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Sample records for phase separated thermotropic

  1. Thermotropic lipid phase separations in human erythrocyte ghosts and cholesterol-enriched rat liver plasma membranes.

    PubMed

    Gordon, L M; Mobley, P W

    1984-01-01

    Electron spin resonance (ESR) studies of human erythrocyte ghosts labeled with 5-nitroxide stearate, I(12,3), indicate that a temperature-dependent lipid phase separation occurs with a high onset at 38 degrees C. Cooling below 38 degrees C induces I(12,3) clustering. Similar phase separations were previously identified in human platelet and cholesterol-loaded [cholesterol/phospholipid molar ratio (C/P) = 0.85] rat liver plasma membranes [L.M. Gordon et al., 1983; J. Membrane Biol. 76; 139-149]; these were attributed to redistribution of endogenous lipid components such that I(12,3) is excluded from cholesterol-rich domains and tends to reside in cholesterol-poor domains. Further enrichment of rat liver plasma membranes to C/P ratios of 0.94-0.98 creates an "artificial" system equivalent to human erythrocyte ghosts (C/P = 0.90), using such criteria as probe flexibility, temperature dependent I(12,3) clustering; and polarity of the probe environment. Consequently, cholesterol-rich and -poor domains probably exist in both erythrocyte ghosts and high cholesterol liver membranes at physiologic temperatures. The temperature dependence of cold-induced hypertonic lysis of intact human erythrocytes was examined by incubating cells in 0.9 M sucrose for 10 min at 1 degree C intervals between 9 and 46 degrees C (Stage 1), and then subjecting them to 0 degrees C for 10 min (Stage 2). Plots of released hemoglobin are approx. sigmoidal, with no lysis below 18 degrees C and maximal lysis above 40 degrees C. The protective effect of low temperatures during Stage 1 may be due to the formation of cholesterol-rich domains that alter the bilayer distribution and/or conformation of critical membrane-associated proteins.

  2. Combined lyotropic and thermotropic phase transitions of deoxycholic acid

    NASA Astrophysics Data System (ADS)

    Vuc˜elić, V.; Vũcelić, D.

    1980-02-01

    Phase transitions of deoxycholic acid have been examined by studying systems which form a clathrate during crystallization. It has been shown that, depending upon the type of solvent molecule present, the deoxycholic acid clathrate may or may not form a thermotropic liquid crystal. In this manner, the simultaneous occurrence of both lyotropic and thermotropic effects was observed.

  3. Skeletal cubic, lamellar, and ribbon phases of bundled thermotropic bolapolyphiles.

    PubMed

    Liu, Feng; Prehm, Marko; Zeng, Xiangbing; Tschierske, Carsten; Ungar, Goran

    2014-05-14

    A series of T-shaped polyphilic molecules composed of a rigid linear biphenyl core with a polar glycerol group at each end and one swallow-tail semiperfluorinated lateral chain were synthesized and their thermotropic liquid crystalline (LC) phases were investigated by X-ray diffraction, calorimetry, and microscopy. The compounds have a long alkyl spacer between the aromatic core and the fluorinated C(n)F(2n+1) ends, where n = 4, 6, 8, and 10. Upon melting, all compounds start with lamellar LC phases, followed on heating by a rectangular columnar ribbon phase with c2mm symmetry. Unusually, a ribbon is a flat bundle of molecular cores highly aligned parallel to the ribbon axis. On further heating, for n = 8 and 10, this phase is succeeded by a bicontinuous cubic phase with Ia3d symmetry. This is a new variant of the "gyroid" phase, with axially oriented rod-like molecular cores forming the skeleton of the two infinite networks and junctions separated by exactly two molecular lengths. In this tricontinuous core-shell structure (aromatic-aliphatic-perfluoroalkyl), the polar glycerol domains of appreciable size, contained within the skeleton, can be considered as micellar.

  4. Thermotropic phase behavior of multilamellar membranes of dioleoylphosphatidylcholine.

    PubMed

    Zhang, Yu-Dong; Lu, Ying; Hu, Shu-Xin; Li, Ming

    2010-02-18

    We use the X-ray diffraction method to examine the thermotropic phase behavior of multilamellar membranes of dioleoylphosphatidylcholine. We find that when the temperature is reduced from room temperature to below 0 degrees C, both the lipid bilayers and the amount of water in the bilayers increase. But the interbilayer distance descends abruptly at a certain temperature between -6 and -15 degrees C, the actual value depending on the relative humidity of the atmosphere, solely due to the thinning of the water layer, d(w). There are several L(alpha) and L(c) phase coexistence states both in the cooling process and in the heating process. In the cooling process, only a part of the lipid molecules accomplish the L(alpha)-to-L(c) main phase transition at -16 degrees C, with the rest of the lipids being frozen down to a very low temperature. In the heating process, however, these frozen lipid molecules are able to move to complete the L(alpha)-to-L(c) main phase transition at -12 degrees C. The reverse of the main phase transition begins at -9 degrees C and is completed at -5 degrees C, after which the water is absorbed into the lipid bilayer to increase the thickness of the water layer, while the thickness of the lipid membranes remain unchanged. This process continues until all the ice on top of the samples melts.

  5. Thermotropic phase transition in soluble nanoscale lipid bilayers

    PubMed Central

    Denisov, Ilia G.; McLean, Mark A.; Shaw, Andrew W.; Grinkova, Yelena V.; Sligar, Stephen G.

    2008-01-01

    The role of lipid domain size and protein-lipid interfaces in the thermotropic phase transition of dipalmitoyl phosphatidylcholine (DPPC) and dimyristoyl phosphatidylcholine (DMPC) bilayers in Nanodiscs was studied using small-angle X-ray scattering (SAXS), differential scanning calorimetry (DSC), and generalized polarization (GP) of the lipophilic probe Laurdan. Nanodiscs are water-soluble, monodisperse self-assembled lipid bilayers encompassed by a helical membrane scaffold protein (MSP). MSPs of different lengths were used to define the diameter of the Nanodisc lipid bilayer from 76 to 108 Å and the number of DPPC molecules from 164 to 335 per discoidal structure. In Nanodiscs of all sizes, the phase transitions were broader and shifted to higher temperatures relative to those observed in vesicle preparations. The size dependences of the transition enthalpies and structural parameters of Nanodiscs reveal the presence of a boundary lipid layer in contact with the scaffold protein encircling the perimeter of the disc. The thickness of this annular layer was estimated to be approximately 15 Å, or two lipid molecules. SAXS was used to measure the lateral thermal expansion of Nanodiscs and a steep decrease of bilayer thickness during the main lipid phase transition was observed. These results provide basis for the quantitative understanding of cooperative phase transitions in membrane bilayers in confined geometries at the nanoscale. PMID:16852976

  6. Phase modulation of thermotropic liquid crystals of tetra-n-alkylammonium polyoxometalate ionic complexes.

    PubMed

    Jiang, Yunxia; Liu, Shuxia; Zhang, Jing; Wu, Lixin

    2013-06-07

    A series of composition analogous polyoxometalate-based ionic complexes are synthesized and studied, with a focus on the correlation between their mesomorphic behavior and their chemical structure. Generally, these polarizable rigid polyoxoanion clusters decorated with hydrophobic flexible alkyl chains have demonstrated a propensity to form thermotropic liquid-crystalline (LC) phases. Characterized by differential scanning calorimetry (DSC), polarized optical microscopy (PM), and X-ray diffraction (XRD), two of the four investigated complexes tend to form thermodynamically stable mesophases. Longer alkyl chains have been found to form mesophases, and the alkyl chain length of the quaternary ammonium cations influences both the occurrence and type of mesophase exhibited.

  7. Formation of a Double Diamond Cubic Phase by Thermotropic Liquid Crystalline Self‐Assembly of Bundled Bolaamphiphiles

    PubMed Central

    Zeng, Xiangbing; Prehm, Marko

    2016-01-01

    Abstract A quaternary amphiphile with swallow‐tail side groups displays a new bicontinuous thermotropic cubic phase with symmetry Pn 3‾ m and formed by two interpenetrating networks where cylindrical segments are linked by H bonds at tetrahedral junctions. Each network segment contains two bundles, each containing 12 rod‐like mesogens, lying along the segment axis. This assembly leads to the first thermotropic structure of the “double diamond” type. A quantitative geometric model is proposed to explain the occurrence of this rare phase. PMID:27270840

  8. Alkyl-bis(imidazolium) salts: a new amphiphile platform that forms thermotropic and non-aqueous lyotropic bicontinuous cubic phases

    SciTech Connect

    Robertson, LA; Schenkel, MR; Wiesenauer, BR; Gin, DL

    2013-01-01

    New ionic amphiphiles with a hexyl-bridged bis(imidazolium) headgroup; Br-, BF4-, or Tf2N- anions; and a long n-alkyl tail can form thermotropic bicontinuous cubic liquid crystal phases in neat form and/or lyotropic bicontinuous cubic phases with several non-aqueous solvents or water.

  9. Structure and Thermotropic phase Behavior of Fluorinated Phospholipid Bilayers: A combined Attenuated Total Reflection FTIR Spectroscopy and Imaging Ellipsometry Study

    PubMed Central

    Schuy, Steffen; Faiss, Simon; Yoder, Nicholas C.; Kalsani, Venkateshwarlu; Kumar, Krishna; Janshoff, Andreas; Vogel, Reiner

    2008-01-01

    Lipid bilayers consisting of lipids with terminally perfluoroalkylated chains have remarkable properties. They exhibit increased stability and phase-separated nanoscale patterns in mixtures with nonfluorinated lipids. In order to understand the bilayer properties that are responsible for this behavior, we have analyzed the structure of solid-supported bilayers composed of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and of a DPPC analogue with 6 terminal perfluorinated methylene units (F6-DPPC). Polarized attenuated total reflection Fourier-transform infrared spectroscopy indicates that for F6-DPPC, the tilt of the lipid acyl chains to the bilayer normal is increased to 39° as compared to 21° for native DPPC, for both lipids in the gel phase. This substantial increase of the tilt angle is responsible for a decrease of the bilayer thickness from 5.4 nm for DPPC to 4.5 nm for F6-DPPC, as revealed by temperature-controlled imaging ellipsometry on microstructured lipid bilayers and solution atomic force microscopy. During the main phase transition from the gel to the fluid phase, both the relative bilayer thickness change and the relative area change are substantially smaller for F6-DPPC than for DPPC. In light of these structural and thermotropic data, we propose a model in which the higher acyl-chain tilt angle in F6-DPPC is the result of a conformational rearrangement to minimize unfavorable fluorocarbon–hydrocarbon interactions in the center of the bilayer due to chain staggering. PMID:18563929

  10. Effect of a glucose-triazole-hydrogenated cardanol conjugate on lipid bilayer membrane organization and thermotropic phase transition

    NASA Astrophysics Data System (ADS)

    Swain, Jitendriya; Kamalraj, M.; Surya Prakash Rao, H.; Mishra, Ashok K.

    2015-02-01

    This work focuses on the membrane perturbation, solubilisation and thermotropic phase transition process of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) MLVs induced by a glucose-triazole-hydrogenated cardanol conjugate (GTHCC). GTHCC is a recently introduced non toxic sugar derivative. Differential scanning calorimetry (DSC) and fluorescence molecular probe based techniques have been used to understand the concentration dependent membrane perturbation, solubilisation and thermotropic phase transition process of DPPC MLVs. The phase transition temperature of DPPC MLVs decreases with increase in mol% of GTHCC. At higher concentration above 10 mol%, GTHCC was significantly perturbed the membrane organization. The intrinsic fluorescence of GTHCC is also found to be sensitive towards phase behaviour and changes in membrane organization of DPPC MLVs.

  11. Effect of ceramide acyl chain length on skin permeability and thermotropic phase behavior of model stratum corneum lipid membranes.

    PubMed

    Janůšová, Barbora; Zbytovská, Jarmila; Lorenc, Petr; Vavrysová, Helena; Palát, Karel; Hrabálek, Alexandr; Vávrová, Kateřina

    2011-03-01

    Stratum corneum ceramides play an essential role in the barrier properties of skin. However, their structure-activity relationships are poorly understood. We investigated the effects of acyl chain length in the non-hydroxy acyl sphingosine type (NS) ceramides on the skin permeability and their thermotropic phase behavior. Neither the long- to medium-chain ceramides (8-24 C) nor free sphingosine produced any changes of the skin barrier function. In contrast, the short-chain ceramides decreased skin electrical impedance and increased skin permeability for two marker drugs, theophylline and indomethacin, with maxima in the 4-6C acyl ceramides. The thermotropic phase behavior of pure ceramides and model stratum corneum lipid membranes composed of ceramide/lignoceric acid/cholesterol/cholesterol sulfate was studied by differential scanning calorimetry and infrared spectroscopy. Differences in thermotropic phase behavior of these lipids were found: those ceramides that had the greatest impact on the skin barrier properties displayed the lowest phase transitions and formed the least dense model stratum corneum lipid membranes at 32°C. In conclusion, the long hydrophobic chains in the NS-type ceramides are essential for maintaining the skin barrier function. However, this ability is not shared by their short-chain counterparts despite their having the same polar head structure and hydrogen bonding ability.

  12. Infrared spectroscopic study of thermotropic phase behavior of newly developed synthetic biopolymers.

    PubMed

    Bista, Rajan K; Bruch, Reinhard F; Covington, Aaron M

    2011-10-15

    The thermotropic phase behavior of a suite of newly developed self-forming synthetic biopolymers has been investigated by variable-temperature Fourier transform infrared (FT-IR) absorption spectroscopy. The temperature-induced infrared spectra of these artificial biopolymers (lipids) composed of 1,2-dimyristoyl-rac-glycerol-3-dodecaethylene glycol (GDM-12), 1,2-dioleoyl-rac-glycerol-3-dodecaethylene glycol (GDO-12) and 1,2-distearoyl-rac-glycerol-3-triicosaethylene glycol (GDS-23) in the spectral range of 4000-500 cm(-1) have been acquired by using a thin layered FT-IR spectrometer in conjunction with a custom built temperature-controlled demountable liquid cell having a pathlength of ∼15 μm. The lipids under consideration have long hydrophobic acyl chains and contain various units of hydrophilic polyethylene glycol (PEG) headgroups. In contrast to conventional phospholipids, this new kind of lipids forms liposomes or nanovesicles spontaneously upon hydration, without requiring external activation energy. We have found that the thermal stability of the PEGylated lipids differs greatly depending upon the acyl chain-lengths as well as the nature of the associated bonds and the number of PEG headgroup units. In particular, GDM-12 (saturated 14 hydrocarbon chains with 12 units of PEG headgroup) exhibits one sharp order-disorder phase transition over a temperature range increasing from 3°C to 5°C. Similarly, GDS-23 (saturated 18 hydrocarbon chains with 23 units of PEG headgroup) displays comparatively broad order-disorder phase transition profiles between temperature 17°C and 22°C. In contrast, GDO-12 (monounsaturated 18 hydrocarbon chains with 12 units of PEG headgroup) does not reveal any order-disorder transition phenomena demonstrating a highly disordered behavior for the entire temperature range. To confirm these observations, differential scanning calorimetry (DSC) was applied to the samples and revealed good agreement with the infrared spectroscopy results

  13. Thermotropic phase behaviour of alpha-dipalmitoylphosphatidylcholine multibilayers is influenced to various extents by carotenoids containing different structural features--evidence from differential scanning calorimetry.

    PubMed

    Kostecka-Gugała, Anna; Latowski, Dariusz; Strzałka, Kazimierz

    2003-01-31

    Carotenoids are the effective modulators of physical properties of model and natural membranes. To demonstrate the relationship between the structure of carotenoids and their effect on the molecular dynamics of membranes, we have investigated the influence of five structurally different carotenoids: beta-carotene, lycopene, lutein, violaxanthin, zeaxanthin and additionally carotane--a fully saturated derivative of beta-carotene, on thermotropic phase behaviour of dipalmitoylphosphatidylcholine (DPPC) multilamellar vesicles by means of differential scanning calorimetry (DSC). The results obtained indicate that the carotenoids used modulated the thermotropic properties of multibilayers to various extents, broadening the pretransition and the main phase transition peaks and shifting them to lower temperatures. Pronounced decrease of pretransition enthalpy (DeltaH(p)) proves that carotenoids very strongly alter the membrane properties in its gel phase. Comparison of the influence of several carotenoids shows that a rigid, polyisoprenoid chain plays a basic role in altering the thermotropic properties of such membranes and the presence of rings without oxygen-containing groups has a minor significance for the observed interactions. Carotenoids containing epoxy and/or hydroxy groups attached to their rings modify the thermotropic phase behaviour of DPPC multilamellar vesicles stronger than carotenes--a result of their orientation in the DPPC bilayer.

  14. The Influence of Disorder on Thermotropic Nematic Liquid Crystals Phase Behavior

    PubMed Central

    Popa-Nita, Vlad; Gerlič, Ivan; Kralj, Samo

    2009-01-01

    We review the theoretical research on the influence of disorder on structure and phase behavior of condensed matter system exhibiting continuous symmetry breaking focusing on liquid crystal phase transitions. We discuss the main properties of liquid crystals as adequate systems in which several open questions with respect to the impact of disorder on universal phase and structural behavior could be explored. Main advantages of liquid crystalline materials and different experimental realizations of random field-type disorder imposed on liquid crystal phases are described. PMID:19865529

  15. Process for phase separation

    DOEpatents

    Comolli, Alfred G.

    1979-01-01

    This invention provides a continuous process for separating a gaseous phase from a hydrocarbon liquid containing carbonaceous particulates and gases. The liquid is fed to a cylindrical separator, with the gaseous phase being removed therefrom as an overhead product, whereas the hydrocarbon liquid and the particulates are withdrawn as a bottoms product. By feeding the liquid tangentially to the separator and maintaining a particulate-liquid slurry downward velocity of from about 0.01 to about 0.25 fps in the separator, a total solids weight percent in the slurry of from about 0.1 to about 30%, a slurry temperature of from about 550.degree. to about 900.degree. F., a slurry residence time in the separator of from about 30 to about 360 seconds, and a length/diameter ratio for the separator of from about 20/1 to about 50/1, so that the characterization factor, .alpha., defined as ##STR1## DOES NOT EXCEED ABOUT 48 (.degree.R sec.sup.2)/ft, the deposit of carbonaceous materials on the interior surface of the separator may be substantially eliminated.

  16. Thermotropic phase transitions in model membranes of the outer skin layer based on ceramide 6

    NASA Astrophysics Data System (ADS)

    Gruzinov, A. Yu.; Kiselev, M. A.; Ermakova, E. V.; Zabelin, A. V.

    2014-01-01

    The lipid intercellular matrix stratum corneum of the outer skin layer is a multilayer membrane consisting of a complex mixture of different lipids: ceramides, fatty acids, cholesterol, and its derivatives. The basis of the multilayer membrane is the lipid bilayer, i.e., a two-dimensional liquid crystal. Currently, it is known that the main way of substance penetration through the skin is the lipid matrix. The complexity of the actual biological system does not allow reliable direct study of its properties; therefore, system modeling is often used. Phase transitions in the lipid system whose composition simulates the native lipid matrix are studied by the X-ray synchrotron radiation diffraction method.

  17. Differential scanning calorimetric and Fourier transform infrared spectroscopic studies of the effects of cholesterol on the thermotropic phase behavior and organization of a homologous series of linear saturated phosphatidylserine bilayer membranes.

    PubMed

    McMullen, T P; Lewis, R N; McElhaney, R N

    2000-10-01

    We have examined the effects of cholesterol on the thermotropic phase behavior and organization of aqueous dispersions of a homologous series of linear disaturated phosphatidylserines by high-sensitivity differential scanning calorimetry and Fourier transform infrared spectroscopy. We find that the incorporation of increasing quantities of cholesterol progressively reduces the temperature, enthalpy, and cooperativity of the gel-to-liquid-crystalline phase transition of the host phosphatidylserine bilayer, such that a cooperative chain-melting phase transition is completely or almost completely abolished at 50 mol % cholesterol, in contrast to the results of previous studies. We are also unable to detect the presence of a separate anhydrous cholesterol or cholesterol monohydrate phase in our binary mixtures, again in contrast to previous reports. We further show that the magnitude of the reduction in the phase transition temperature induced by cholesterol addition is independent of the hydrocarbon chain length of the phosphatidylserine studied. This result contrasts with our previous results with phosphatidylcholine bilayers, where we found that cholesterol increases or decreases the phase transition temperature in a chain length-dependent manner (1993. Biochemistry, 32:516-522), but is in agreement with our previous results for phosphatidylethanolamine bilayers, where no hydrocarbon chain length-dependent effects were observed (1999. Biochim. Biophys. Acta, 1416:119-234). However, the reduction in the phase transition temperature by cholesterol is of greater magnitude in phosphatidylethanolamine as compared to phosphatidylserine bilayers. We also show that the addition of cholesterol facilitates the formation of the lamellar crystalline phase in phosphatidylserine bilayers, as it does in phosphatidylethanolamine bilayers, whereas the formation of such phases in phosphatidylcholine bilayers is inhibited by the presence of cholesterol. We ascribe the limited

  18. Calorimetric and spectroscopic studies of the thermotropic phase behavior of lipid bilayer model membranes composed of a homologous series of linear saturated phosphatidylserines.

    PubMed Central

    Lewis, R N; McElhaney, R N

    2000-01-01

    The thermotropic phase behavior of lipid bilayer model membranes composed of the even-numbered, N-saturated 1,2-diacyl phosphatidylserines was studied by differential scanning calorimetry and by Fourier-transform infrared and (31)P-nuclear magnetic resonance spectroscopy. At pH 7.0, 0.1 M NaCl and in the absence of divalent cations, aqueous dispersions of these lipids, which have not been incubated at low temperature, exhibit a single calorimetrically detectable phase transition that is fully reversible, highly cooperative, and relatively energetic, and the transition temperatures and enthalpies increase progressively with increases in hydrocarbon chain length. Our spectroscopic observations confirm that this thermal event is a lamellar gel (L(beta))-to-lamellar liquid crystalline (L(alpha)) phase transition. However, after low temperature incubation, the L(beta)/L(alpha) phase transition of dilauroyl phosphatidylserine is replaced by a higher temperature, more enthalpic, and less cooperative phase transition, and an additional lower temperature, less enthalpic, and less cooperative phase transition appears in the longer chain phosphatidylserines. Our spectroscopic results indicate that this change in thermotropic phase behavior when incubated at low temperatures results from the conversion of the L(beta) phase to a highly ordered lamellar crystalline (L(c)) phase. Upon heating, the L(c) phase of dilauroyl phosphatidylserine converts directly to the L(alpha) phase at a temperature slightly higher than that of its original L(beta)/L(alpha) phase transition. Calorimetrically, this process is manifested by a less cooperative but considerably more energetic, higher-temperature phase transition, which replaces the weaker L(beta)/L(alpha) phase transition alluded to above. However, with the longer chain compounds, the L(c) phase first converts to the L(beta) phase at temperatures some 10-25 degrees C below that at which the L(beta) phase converts to the L(alpha) phase

  19. Nematic-nematic demixing in polydisperse thermotropic liquid crystals

    NASA Astrophysics Data System (ADS)

    Sollich, Peter

    2005-06-01

    We consider the effects of polydispersity on isotropic-nematic phase equilibria in thermotropic liquid crystals, using a Maier-Saupe theory [Z. Naturforsch. A 13A, 564 (1958)] with factorized interactions. A sufficient spread (≈50%) in the interaction strengths of the particles leads to phase separation into two or more nematic phases, which can in addition coexist with an isotropic phase. The isotropic-nematic coexistence region widens dramatically as polydispersity is increased, leading to reentrant isotropic-nematic phase separation in some regions of the phase diagram. We show that similar phenomena will occur also for nonfactorized interactions as long as the interaction strength between any two particle species is lower than the mean of the intraspecies interactions.

  20. Microgravity Passive Phase Separator

    NASA Technical Reports Server (NTRS)

    Paragano, Matthew; Indoe, William; Darmetko, Jeffrey

    2012-01-01

    A new invention disclosure discusses a structure and process for separating gas from liquids in microgravity. The Microgravity Passive Phase Separator consists of two concentric, pleated, woven stainless- steel screens (25-micrometer nominal pore) with an axial inlet, and an annular outlet between both screens (see figure). Water enters at one end of the center screen at high velocity, eventually passing through the inner screen and out through the annular exit. As gas is introduced into the flow stream, the drag force exerted on the bubble pushes it downstream until flow stagnation or until it reaches an equilibrium point between the surface tension holding bubble to the screen and the drag force. Gas bubbles of a given size will form a front that is moved further down the length of the inner screen with increasing velocity. As more bubbles are added, the front location will remain fixed, but additional bubbles will move to the end of the unit, eventually coming to rest in the large cavity between the unit housing and the outer screen (storage area). Owing to the small size of the pores and the hydrophilic nature of the screen material, gas does not pass through the screen and is retained within the unit for emptying during ground processing. If debris is picked up on the screen, the area closest to the inlet will become clogged, so high-velocity flow will persist farther down the length of the center screen, pushing the bubble front further from the inlet of the inner screen. It is desired to keep the velocity high enough so that, for any bubble size, an area of clean screen exists between the bubbles and the debris. The primary benefits of this innovation are the lack of any need for additional power, strip gas, or location for venting the separated gas. As the unit contains no membrane, the transport fluid will not be lost due to evaporation in the process of gas separation. Separation is performed with relatively low pressure drop based on the large surface

  1. Surface alignment, anchoring transitions, optical properties, and topological defects in the nematic phase of thermotropic bent-core liquid crystal A131

    NASA Astrophysics Data System (ADS)

    Senyuk, B.; Wonderly, H.; Mathews, M.; Li, Q.; Shiyanovskii, S. V.; Lavrentovich, O. D.

    2010-10-01

    We study optical, structural, and surface anchoring properties of thermotropic nematic bent-core material A131. The focus is on the features associated with orientational order as the material has been reported to exhibit not only the usual uniaxial nematic but also the biaxial nematic phase. We demonstrate that A131 experiences a surface anchoring transition from a perpendicular to tilted alignment when the temperature decreases. The features of the tilted state are consistent with surface-induced birefringence associated with smectic layering near the surface and a molecular tilt that changes along the normal to the substrates. The surface-induced birefringence is reduced to zero by a modest electric field that establishes a uniform uniaxial nematic state. Both refractive and absorptive optical properties of A131 are consistent with the uniaxial order. We found no evidence of the “polycrystalline” biaxial behavior in the cells placed in crossed electric and magnetic fields. We observe stable topological point defects (boojums and hedgehogs) and nonsingular “escaped” disclinations pertinent only to the uniaxial order. Finally, freely suspended films of A131 show uniaxial nematic and smectic textures; a decrease in the film thickness expands the temperature range of stability of smectic textures, supporting the idea of surface-induced smectic layering. Our conclusion is that A131 features only a uniaxial nematic phase and that the apparent biaxiality is caused by subtle surface effects rather than by the bulk biaxial phase.

  2. Microcellular foams via phase separation

    SciTech Connect

    Young, A.T.

    1985-01-01

    A study of wide variety of processes for making plastic foams shows that phase separation processes for polymers from solutions offers the most viable methods for obtaining rigid plastic foams which met the physical requirements for fusion target designs. Four general phase separation methods have been shown to give polymer foams with densities less than 0.1 g/cm/sup 3/ and cell sizes of 30..mu..m or less. These methods involve the utilization of non-solvent, chemical or thermal cooling processes to achieve a controlled phase separation wherein either two distinct phases are obtained where the polymer phase is a continuous phase or two bicontinuous phases are obtained where both the polymer and solvent are interpenetrating, continuous, labyrinthine phases. Subsequent removal of the solvent gives the final foam structure.

  3. 19F single-quantum and 19F-33S heteronuclear multiple-quantum coherence NMR of SF6 in thermotropic nematogens and in the gas phase.

    PubMed

    Tervonen, Henri; Saunavaara, Jani; Ingman, L Petri; Jokisaari, Jukka

    2006-08-24

    (19)F single-quantum (SQC) and (19)F-(33)S heteronuclear multiple-quantum coherence (HMQC) NMR spectroscopy of sulfur hexafluoride (SF(6)) dissolved in thermotropic liquid crystals (TLCs) were used to investigate the properties of TLCs. On one hand, environmental effects on the NMR parameters of SF(6), (19)F nuclear shielding, (19)F-(33)S spin-spin coupling, secondary isotope effects of sulfur on (19)F shielding, and the self-diffusion coefficient in the direction of the external magnetic field were studied as well. The temperature dependence of the (19)F shielding of SF(6) in TLCs was modeled with a function that takes into account the properties of both TLC and SF(6). It appears that the TLC environment deforms the electronic system of SF(6) so that the (19)F shielding tensor becomes slightly anisotropic, with the anisotropy being from -0.5 to -1.4 ppm, depending upon the TLC solvent. On the contrary, no sign of residual dipolar coupling between (19)F and (33)S was found, meaning that the so-called deformational effects, which arise from the interaction between vibrational and reorientational motions of the molecule, on the geometry of the molecule are insignificant. Diffusion activation energies, E(a), were determined from the temperature dependence of the self-diffusion coefficients. In each TLC, E(a) increases when moving from an isotropic phase to a nematic phase. The spin-spin coupling constant, J((19)F,(33)S), increases by ca. 10 Hz when moving from the gas phase to TLC solutions. The secondary isotope shifts of (19)F shielding are practically independent of TLC solvent and temperature. For the first time, (19)F-(33)S heteronuclear multiple-quantum NMR spectra were recorded for SF(6) in the gas phase and in a liquid-crystalline solution.

  4. Sterol chemical configuration influences the thermotropic phase behaviour of dipalmitoylphosphatidylcholine bilayers containing 5α-cholestan-3β- and 3α-ol.

    PubMed

    Benesch, Matthew G K; Mannock, David A; McElhaney, Ronald N

    2011-01-01

    It is commonly believed that all membrane sterols are rigid all-trans ring systems with a fully extended alkyl side-chain and that they similarly influence phospholipid bilayer physical properties. Here, we report the sterol concentration-dependent, thermotropic phase behaviour of binary dipalmitoylphosphatidylcholine (DPPC)/sterol mixtures containing two similar 5α-H sterols with different functional group orientations (3α-OH or 3β-OH), which adopt an ideal all-trans planar ring conformation but lack the deformed ring B conformation of cholesterol (Chol) and epicholesterol (Echol), using differential scanning calorimetry (DSC). Our deconvolution of the DSC main phase transition endotherms show differences in the proportions of sterol-poor (sharp) and sterol-rich (broad) domains in the DPPC bilayer with increasing sterol concentration, which delineate gel/liquid-crystalline (P(β')/L(α)) and disordered gel (L(β))/liquid-ordered (l(o)) phase regions. There are similarities in the DPPC main phase transition temperature, cooperativity and enthalpy for each 3β-ol and 3α-ol pair with increasing sterol concentration and differences in the parameters obtained for both the sterol-poor and sterol-rich regions. The sterol-poor domain persists over a greater concentration range in both 3α-ol/DPPC mixtures, suggesting that either those domains are more stable in the 3α-ols or that those sterols are less miscible in the sterol-rich domain. Corresponding parameters for the sterol-rich domain show that at sterol concentrations up to 20mol%, the 5α-H,3β-ol is more effective at reducing the phase transition enthalpy of the broad component (ΔH(m)(brd)) than Chol, but is less effective at higher concentrations. Although mixtures containing Echol and 5α-cholestan-3α-ol have similar positive slopes below 7mol% sterol, suggesting that they abolish the L(β)/l(o) phase transition equally effectively at low concentrations, Echol is more effective than the saturated 3α-ol at

  5. Thermotropic lateral translational motion of intramembrane particles in the inner mitochondrial membrane and its inhibition by artificial peripheral proteins

    PubMed Central

    1977-01-01

    Freeze fracturing and deep etching have been used to study thermotropic lateral translational motion of intramembrane particles and membrane surface anionic groups in the inner mitochondrial membrane. When the inner membrane is equilibrated at low temperature, the fracture faces of both halves of the membrane reveal a lateral separation between intramembrane particles and particle free, large smooth patches. Such separation is completely reversed through free lateral translational diffusion by reversing the temperature. The low temperature induced, particle-free, smooth membrane patches appear to represent regions of protein-excluding, ordered bilayer lipid which form during thermotropic liquid crystalline to gel state phase transitions. When polycationic ferritin is electrostatically bound to anionic groups exposed at the membrane surface at concentrations which inhibit the activities of cytochrome c oxidase and succinate permease, the bound ferritin migrates with intramembrane particles during the thermotropic lateral separation between the membrane particles and smooth patches. When bound polycationic ferritin is cross-bridged with native ferritin, an artificial peripheral protein lattice forms in association with the surface anionic groups and diminishes the thermotropic lateral translational motion of intramembrane particles in the membrane. These results reveal that the anionic groups of metabolically active integral proteins which are known to be exposed at the surface of the inner mitochondrial membrane migrate with intramembrane particles in the plane of the membrane under conditions which induce lipid-protein lateral separations. In addition, cross-bridging of the anionic groups through an artificial peripheral protein lattice appears to diminish such induced lipid protein lateral separations. PMID:833199

  6. Thermotropic behavior of binary mixtures of dipalmitoylphosphatidylcholine and glycosphingolipids in aqueous dispersions.

    PubMed

    Maggio, B; Ariga, T; Sturtevant, J M; Yu, R K

    1985-08-08

    The thermotropic behavior of mixtures of dipalmitoylphosphatidylcholine (DPPC) with natural glycosphingolipids (galactosylceramide, phrenosine, kerasine, glucosylceramide, lactosylceramide, asialo-GM1, sulfatide, GM3, GM1, GD1a, GT1b) in dilute aqueous dispersions were studied by high sensitivity differential scanning calorimetry over the entire composition range. The pretransition of DPPC is abolished and the cooperativity of the main transition decreases sharply at mole fractions of glycosphingolipids below 0.2. All systems exhibit non-ideal temperature-composition phase diagrams. The mono- and di-hexosylceramides are easily miscible with DPPC when the proportion of glycosphingolipids in the system is high. A limited quantity (1-6 molecules of DPPC per molecule of glycosphingolipid (GSL) can be incorporated into a homogeneously mixed lipid phase. Domains of DPPC, immiscible with the rest of a mixed GSL-DPPC phase that shows no cooperative phase transition, are established as DPPC exceeds a certain proportion in the system. One negative charge (sulfatide) or four neutral carbohydrate residues (asialo-GM1) in the oligosaccharide chain of the glycosphingolipids results in phase diagrams exhibiting coexistence of gel and liquid phases over a broad temperature-composition range. Systems containing gangliosides show complex phase diagrams, with more than one phase transition. However, no evidence for phase-separated domains of pure ganglioside species is found. The thermotropic behavior of systems containing DPPC and glycosphingolipids correlates well with their interactions in mixed monolayers at the air/water interface.

  7. Role of Molecular Structure on X-ray Diffraction in Uniaxial and Biaxial Phases of Thermotropic Liquid Crystals

    SciTech Connect

    Acharya, Bharat R.; Kang, Shin-Woong; Prasad, Veena; Kumar, Satyendra

    2009-04-29

    X-ray diffraction is one of the most definitive methods to determine the structure of condensed matter phases, and it has been applied to unequivocally infer the structures of conventional calamitic and lyotropic liquid crystals. With the advent of bent-core and tetrapodic mesogens and the discovery of the biaxial nematic phase in them, the experimental results require more careful interpretation and analysis. Here, we present ab-initio calculations of X-ray diffraction patterns in the isotropic, uniaxial nematic, and biaxial nematic phases of bent-core mesogens. A simple Meier-Saupe-like molecular distribution function is employed to describe both aligned and unaligned mesophases. The distribution function is decomposed into two, polar and azimuthal, distribution functions to calculate the effect of the evolution of uniaxial and biaxial nematic orientational order. The calculations provide satisfactory semiquantitative interpretations of experimental results. The calculations presented here should provide a pathway to more refined and quantitative analysis of X-ray diffraction data from the biaxial nematic phase.

  8. Role of Molecular Structure on X-ray Diffraction in Thermotropic Uniaxial and Biaxial Nematic Liquid Crystal Phases

    SciTech Connect

    Acharya, Bharat R.; Kang, Shin-Woong; Prasad, Veena; Kumar, Satyendra

    2009-08-27

    X-ray diffraction is one of the most definitive methods to determine the structure of condensed matter phases, and it has been applied to unequivocally infer the structures of conventional calamitic and lyotropic liquid crystals. With the advent of bent-core and tetrapodic mesogens and the discovery of the biaxial nematic phase in them, the experimental results require more careful interpretation and analysis. Here, we present ab-initio calculations of X-ray diffraction patterns in the isotropic, uniaxial nematic, and biaxial nematic phases of bent-core mesogens. A simple Meier-Saupe-like molecular distribution function is employed to describe both aligned and unaligned mesophases. The distribution function is decomposed into two, polar and azimuthal, distribution functions to calculate the effect of the evolution of uniaxial and biaxial nematic orientational order. The calculations provide satisfactory semiquantitative interpretations of experimental results. The calculations presented here should provide a pathway to more refined and quantitative analysis of X-ray diffraction data from the biaxial nematic phase.

  9. Triblock polyphiles through click chemistry: self-assembled thermotropic cubic phases formed by micellar and monolayer vesicular aggregates.

    PubMed

    Tan, Xiaoping; Kong, Leiyang; Dai, Heng; Cheng, Xiaohong; Liu, Feng; Tschierske, Carsten

    2013-11-25

    Three series of triblock polyphiles consisting of a rigid 4-phenyl-1,2,3-triazole or 1,4-diphenyl-1,2,3-triazole core with three lipophilic and flexible alkoxyl chains at one end and a polar glycerol group at the opposite end were synthesized by copper-catalyzed azide-alkyne click reactions. Their mesophase behavior was studied by polarizing optical microscopy, differential scanning calorimetry, and XRD. Depending on alkyl chain length and core length, a transition from hexagonal columnar to Pm3n-type cubic phases was observed. In the cubic phases, the molecules are organized as spherical objects. Remarkably, compounds with a longer core unit have a higher tendency to form these cubic phases, and their stability is strongly enhanced over those of the compounds with a shorter core, despite longer cores having a smaller cone angle and therefore being expected to disfavor the formation of spherical objects. There is a large difference in the number of molecules involved in the spherical aggregates formed by compounds with long and short cores. Whereas the aggregates in the cubic phases of the compounds with short rod units are small and could be regarded as micellar, the long-core compounds form much larger aggregates which are regarded as a kind of monolayer vesicular aggregate.

  10. Myelin structures formed by thermotropic smectic liquid crystals.

    PubMed

    Peddireddy, Karthik; Kumar, Pramoda; Thutupalli, Shashi; Herminghaus, Stephan; Bahr, Christian

    2013-12-17

    We report on transient structures, formed by thermotropic smectic-A liquid crystals, resembling the myelin figures of lyotropic lamellar liquid crystals. The thermotropic myelin structures form during the solubilization of a smectic-A droplet in an aqueous phase containing a cationic surfactant at concentrations above the critical micelle concentration. Similar to the lyotropic myelin figures, the thermotropic myelins appear in an optical microscope as flexible tubelike structures growing at the smectic/aqueous interface. Polarizing microscopy and confocal fluorescence microscopy show that the smectic layers are parallel to the tube surface and form a cylindrically bent arrangement around a central line defect in the tube. We study the growth behavior of this new type of myelins and discuss similarities to and differences from the classical lyotropic myelin figures.

  11. Formation and characterization of phospholipid monolayers spontaneously assembled at interfaces between aqueous phases and thermotropic liquid crystals.

    PubMed

    Brake, Jeffrey M; Daschner, Maren K; Abbott, Nicholas L

    2005-03-15

    This paper reports an experimental investigation of the self-assembly of phospholipids (l-alpha-phosphatidylcholine-beta-oleoyl-gamma-palmitoyl (l-POPC), dipalmitoyl phosphatidylcholine (DPPC), and l-alpha-dilauroyl phosphatidylcholine (l-DLPC)) at interfaces between aqueous phases and the nematic liquid crystal (LC) 4'-pentyl-4-cyanobiphenyl. Stable planar interfaces between the aqueous phases and LCs were created by hosting the LCs within gold grids (square pores with widths of 283 microm and depths of 20 microm). At these interfaces, the presence and lateral organization of the phospholipids leads to interface-driven orientational transitions within the LC. By doping the phospholipids with a fluorescently labeled lipid (Texas Red-1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (TR-DPPE)), quantitative epifluorescence microscopy revealed the saturation coverage of phospholipid at the interface to be that of a monolayer with an areal density of approximately 49 +/- 8% relative to hydrated lipid bilayers. By adsorbing phospholipids to the aqueous-LC interface from either vesicles or mixed micelles of dodecyltrimethylammonium and phospholipid, control of the areal density of phospholipid from 42 +/- 10 to 102 +/-18% of saturation monolayer coverage was demonstrated. Fluorescence recovery after photobleaching (FRAP) experiments performed by using laser scanning confocal microscopy (LSCM) revealed the lateral mobility of fluorescently labeled DPPE in l-DLPC assembled at the interface with the liquid crystal to be (6 +/- 1) x 10(-12) m(2)/s for densely packed monolayers. Variation of the surface coverage and composition of phospholipid led to changes in lateral diffusivity between (0.2 +/- 0.1) x 10(-12) and (15 +/- 2) x 10(-12) m(2)/s. We also observed the phospholipid-laden interface to be compartmentalized by the gold grid, thus allowing for the creation of patterned arrays of phospholipids at the LC-aqueous interface.

  12. Imaging the oxidation effects of the Fenton reaction on phospholipids at the interface between aqueous phase and thermotropic liquid crystals.

    PubMed

    Zhang, Minmin; Jang, Chang-Hyun

    2015-08-01

    The lipid peroxidation process has attracted much attention because of the growing evidence of its involvement in the pathogenesis of age-related diseases. Herein, we report a simple, label-free method to study the oxidation of phospholipids by the Fenton reaction at the interface between an aqueous phase and immiscible liquid crystals (LCs). The different images produced by the orientation of 4-cyano-4'-pentylbiphenyl (5CB) corresponded to the presence or absence of oxidized 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt (DOPG). The oxidation effects of the Fenton reaction on DOPG were evaluated by monitoring the orientational response of liquid crystals upon contact with the oxidized DOPG solutions. DOPG was oxidized into chain-changed products containing hydroxy, carbonyl, or aldehyde groups, resulting in the rearrangement of the phospholipid layer. This induced the orientational transition of LCs from homeotropic to planar states; therefore, a dark to bright optical shift was observed. This shift was due to the Fenton reaction preventing DOPG to induce the orientational alignment of LCs at the aqueous/LC interface. We also used an ultraviolet spectrophotometer to confirm the effects of oxidation on phospholipids by the Fenton reaction. Using this simple method, a new approach for investigating phospholipid oxidation was established with high resolution and easy accessibility.

  13. Vapors-liquid phase separator

    NASA Astrophysics Data System (ADS)

    Frederking, T. H. K.; Brown, G. S.; Chuang, C.; Kamioka, Y.; Kim, Y. I.; Lee, J. M.; Yuan, S. W. K.

    1980-10-01

    The use of porous plugs, mostly with in the form of passive devices with constant area were considered as vapor-liquid phase separators for helium 2 storage vessels under reduced gravity. The incorporation of components with variable cross sectional area as a method of flow rate modification was also investigated. A particular device which uses a shutter-type system for area variation was designed and constructed. This system successfully permitted flor rate changes of up to plus or minus 60% from its mean value.

  14. Two-Phase Flow Separator Investigation

    NASA Video Gallery

    The goal of the Two-Phase Flow Separator investigation is to help increase understanding of how to separate gases and liquids in microgravity. Many systems on the space station contain both liquids...

  15. Chaotic background phase matching signal separation method

    NASA Astrophysics Data System (ADS)

    Peng, Wu; Hui, Xia; Chen, Wang

    2016-07-01

    Aiming at the problem of separating the useful signal in the chaos background and using the phase matching method, the signal can be extracted effectively from the chaotic background. In this method, the chaotic background is not estimated with phase reconstruction and the geometric analysis of phase space is not required. Through the separation Simulation of the sinusoidal signal in the chaos background and the separation degree analysis, the low signal to noise ratio of the signal in the chaos background can be effectively separated. The effect of removing the chaotic background noise is obvious.

  16. Binary Colloidal Alloy Test-5: Phase Separation

    NASA Technical Reports Server (NTRS)

    Lynch, Matthew; Weitz, David A.; Lu, Peter J.

    2008-01-01

    The Binary Colloidal Alloy Test - 5: Phase Separation (BCAT-5-PhaseSep) experiment will photograph initially randomized colloidal samples onboard the ISS to determine their resulting structure over time. This allows the scientists to capture the kinetics (evolution) of their samples, as well as the final equilibrium state of each sample. BCAT-5-PhaseSep studies collapse (phase separation rates that impact product shelf-life); in microgravity the physics of collapse is not masked by being reduced to a simple top and bottom phase as it is on Earth.

  17. Study Of Phase Separation In Glass

    NASA Technical Reports Server (NTRS)

    Neilson, George F.; Weinberg, Michael C.; Smith, Gary L.

    1989-01-01

    Report describes an experimental study of effect of hydroxide content on phase separation in soda/silica glasses. Ordinary and gel glasses melted at 1,565 degree C, and melts stirred periodically. "Wet" glasses produced by passing bubbles of N2 saturated with water through melts; "dry" glasses prepared in similar manner, except N2 dried before passage through melts. Analyses of compositions of glasses performed by atomic-absorption and index-of-refraction measurements. Authors conclude hydroxide speeds up phase separation, regardless of method (gel or ordinary) by which glass prepared. Eventually helps material scientists to find ways to control morphology of phase separation.

  18. Thermotropic phase behavior of model membranes composed of phosphatidylcholines containing cis-monounsaturated acyl chain homologues of oleic acid: differential scanning calorimetric and /sup 31/P NMR spectroscopic studies

    SciTech Connect

    Lewis, R.N.A.H.; Sykes, B.D.; McElhaney, R.N.

    1988-02-09

    The thermotropic phase behavior of dioleoylphosphatidylcholine and six of its longer chain homologues was studied by differential scanning calorimetry and /sup 31/P nuclear magnetic resonance (NMR) spectroscopy. Aqueous dispersions of these compounds all exhibit a single endotherm upon heating but upon cooling exhibit at least two exotherms, both of which occur at temperatures lower than those of their heating endotherm. The single transition observed upon heating was shown by /sup 31/P NMR spectroscopy to be a net conversion from a condensed, subgel-like phase (L/sub c/ phase) to the liquid-crystalline state. Aqueous ethylene glycol dispersions of these compounds also exhibit single endotherms upon heating and cooling exotherms centered at temperatures lower than those of their corresponding heating endotherm. However, the behavior of the aqueous ethylene glycol dispersions differs with respect to their transition temperatures and enthalpies as well as the extent of undercooling observed, and there is some evidence of discontinuities in the cooling behavior of the odd- and even-numbered members of the homologous series. Like the aqueous dispersions, /sup 31/P NMR spectroscopy also shows that the calorimetric events observed in aqueous ethylene glycol involve net interconversions between an L/sub c/-like phase and the liquid-crystalline state. These results demonstrate that although the presence of a cis double bond can perturb the solid-state packing of the acyl chains, its presence does not preclude the formation of highly ordered subgel-like phases in lipid bilayers. In the particular case of these unsaturated phosphatidylcholines, the formation of the subgel phases is more kinetically favorable than is the case with their saturated n-acyl counterparts.

  19. Vapor-liquid phase separator studies

    NASA Technical Reports Server (NTRS)

    Yuan, S. W. K.; Lee, J. M.; Kim, Y. I.; Hepler, W. A.; Frederking, T. H. K.

    1983-01-01

    Porous plugs serve as both entropy rejection devices and phase separation components separating the vapor phase on the downstream side from liquid Helium 2 upstream. The liquid upstream is the cryo-reservoir fluid needed for equipment cooling by means of Helium 2, i.e Helium-4 below its lambda temperature in near-saturated states. The topics outlined are characteristic lengths, transport equations and plug results.

  20. Gas-Liquid Flows and Phase Separation

    NASA Technical Reports Server (NTRS)

    McQuillen, John

    2004-01-01

    Common issues for space system designers include:Ability to Verify Performance in Normal Gravity prior to Deployment; System Stability; Phase Accumulation & Shedding; Phase Separation; Flow Distribution through Tees & Manifolds Boiling Crisis; Heat Transfer Coefficient; and Pressure Drop.The report concludes:Guidance similar to "A design that operates in a single phase is less complex than a design that has two-phase flow" is not always true considering the amount of effort spent on pressurizing, subcooling and phase separators to ensure single phase operation. While there is still much to learn about two-phase flow in reduced gravity, we have a good start. Focus now needs to be directed more towards system level problems .

  1. Phase Separation in Solutions of Monoclonal Antibodies

    NASA Astrophysics Data System (ADS)

    Benedek, George; Wang, Ying; Lomakin, Aleksey; Latypov, Ramil

    2012-02-01

    We report the observation of liquid-liquid phase separation (LLPS) in a solution of humanized monoclonal antibodies, IgG2, and the effects of human serum albumin, a major blood protein, on this phase separation. We find a significant reduction of phase separation temperature in the presence of albumin, and a preferential partitioning of the albumin into the antibody-rich phase. We provide a general thermodynamic analysis of the antibody-albumin mixture phase diagram and relate its features to the magnitude of the effective inter-protein interactions. Our analysis suggests that additives (HSA in this report), which have moderate attraction with antibody molecules, may be used to forestall undesirable protein condensation in antibody solutions. Our findings are relevant to understanding the stability of pharmaceutical solutions of antibodies and the mechanisms of cryoglobulinemia.

  2. Phase separations in a copolymer copolymer mixture

    NASA Astrophysics Data System (ADS)

    Zhang, Jin-Jun; Jin, Guojun; Ma, Yuqiang

    2006-01-01

    We propose a three-order-parameter model to study the phase separations in a diblock copolymer-diblock copolymer mixture. The cell dynamical simulations provide rich information about the phase evolution and structural formation, especially the appearance of onion-rings. The parametric dependence and physical reason for the domain growth of onion-rings are discussed.

  3. Charge regularization in phase separating polyelectrolyte solutions.

    PubMed

    Muthukumar, M; Hua, Jing; Kundagrami, Arindam

    2010-02-28

    Theoretical investigations of phase separation in polyelectrolyte solutions have so far assumed that the effective charge of the polyelectrolyte chains is fixed. The ability of the polyelectrolyte chains to self-regulate their effective charge due to the self-consistent coupling between ionization equilibrium and polymer conformations, depending on the dielectric constant, temperature, and polymer concentration, affects the critical phenomena and phase transitions drastically. By considering salt-free polyelectrolyte solutions, we show that the daughter phases have different polymer charges from that of the mother phase. The critical point is also altered significantly by the charge self-regularization of the polymer chains. This work extends the progress made so far in the theory of phase separation of strong polyelectrolyte solutions to a higher level of understanding by considering chains which can self-regulate their charge.

  4. A calorimetric and spectroscopic comparison of the effects of cholesterol and its sulfur-containing analogs thiocholesterol and cholesterol sulfate on the thermotropic phase behavior and organization of dipalmitoylphosphatidylcholine bilayer membranes.

    PubMed

    Benesch, Matthew G K; Lewis, Ruthven N A H; McElhaney, Ronald N

    2016-02-01

    We performed differential scanning calorimetric (DSC) and Fourier transform infrared (FTIR) spectroscopic studies of the effects of cholesterol (Chol), thiocholesterol (tChol) and cholesterol sulfate (CholS) on the thermotropic phase behavior and organization of dipalmitoylphosphatidylcholine (DPPC) bilayer membranes. Our DSC results indicate that Chol and tChol incorporation produce small temperature increases in the main phase transition broad component while CholS markedly decreases it, but Chol decreases cooperativity and enthalpy more strongly than CholS and especially tChol. Hence, Chol and tChol thermally stabilize fluid DPPC bilayer sterol-rich domains while CholS markedly destabilizes them, and CholS and particularly tChol are less miscible in such domains. Our FTIR spectroscopic results indicate that Chol incorporation increases the rotational conformational order of fluid DPPC bilayers to a slightly and somewhat greater degree than tChol and CholS, respectively, consistent with our DSC findings. Also, Chol and CholS produce comparable degrees of H-bonding (hydration) of the DPPC ester carbonyls in fluid bilayers, whereas tChol increases H-bonding. At low temperatures, Chol is fully soluble in gel-state DPPC bilayers, whereas tChol and CholS are not. Thus tChol and CholS incorporation can produce considerably different effects on DPPC bilayers. In particular, the tChol thiol group markedly reduces its lateral miscibility and increases DPPC carbonyl H-bonding without significantly affecting the other characteristic effects of Chol itself, while the CholS sulfate group significantly reduces its ability to thermally stabilize and order fluid DPPC membranes. This latter result suggests that the molecular basis for the purported ability of CholS to "stabilize" various biological membranes should be re-examined.

  5. Impact of the long chain omega-acylceramides on the stratum corneum lipid nanostructure. Part 1: Thermotropic phase behaviour of CER[EOS] and CER[EOP] studied using X-ray powder diffraction and FT-Raman spectroscopy.

    PubMed

    Kessner, Doreen; Brezesinski, Gerald; Funari, Sergio S; Dobner, Bodo; Neubert, Reinhard H H

    2010-01-01

    The stratum corneum (SC), the outermost layer of the mammalian skin, is the main skin barrier. Ceramides (CERs) as the major constituent of the SC lipid matrix are of particular interest. At the moment, 11 classes of CERs are identified, but the effect of each single ceramide species is still not known. Therefore in this article, the thermotropic behaviour of the long chain omega-acylceramides CER[EOS] and CER[EOP] was studied using X-ray powder diffraction and FT-Raman spectroscopy. It was found that the omega-acylceramides CER[EOS] and CER[EOP] do not show a pronounced polymorphism which is observed for shorter chain ceramides as a significant feature. The phase behaviour of both ceramides is strongly influenced by the extremely long acyl-chain residue. The latter has a much stronger influence compared with the structure of the polar head group, which is discussed as extremely important for the appearance of a rich polymorphism. Despite the strong influence of the long chain, the additional OH-group of the phyto-sphingosine type CER[EOP] influences the lamellar repeat distance and the chain packing. The less polar sphingosine type CER[EOS] is stronger influenced by the long acyl-chain residue. Hydration is necessary for the formation of an extended hydrogen-bonding network between the polar head groups leading to the appearance of a long-periodicity phase (LPP). In contrast, the more polar CER[EOP] forms the LPP with densely packed alkyl chains already in the dry state.

  6. Thermotropic phase properties of 1,2-di-O-tetradecyl-3-O-(3-O-methyl- beta-D-glucopyranosyl)-sn-glycerol.

    PubMed Central

    Trouard, T P; Mannock, D A; Lindblom, G; Rilfors, L; Akiyama, M; McElhaney, R N

    1994-01-01

    The hydration properties and the phase structure of 1,2-di-O-tetradecyl-3-O(3-O-methyl-beta-D-glucopyranosyl)-sn-glycerol (3-O-Me-beta-D-GlcDAIG) in water have been studied via differential scanning calorimetry, 1H-NMR and 2H-NMR spectroscopy, and x-ray diffraction. Results indicate that this lipid forms a crystalline (Lc) phase up to temperatures of 60-70 degrees C, where a transition through a metastable reversed hexagonal (Hll) phase to a reversed micellar solution (L2) phase occurs. Experiments were carried out at water concentrations in a range from 0 to 35 wt%, which indicate that all phases are poorly hydrated, taking up < 5 mol water/mol lipid. The absence of a lamellar liquid crystalline (L alpha) phase and the low levels of hydration measured in the discernible phases suggest that the methylation of the saccharide moiety alters the hydrogen bonding properties of the headgroup in such a way that the 3-O-Me-beta-D-GlcDAIG headgroup cannot achieve the same level of hydration as the unmethylated form. Thus, in spite of the small increase in steric bulk resulting from methylation, there is an increase in the tendency of 3-O-Me-beta-D-GlcDAIG to form nonlamellar structures. A similar phase behavior has previously been observed for the Acholeplasma laidlawii A membrane lipid 1,2-diacyl-3-O-(6-O-acyl-alpha-D-glucopyranosyl)-sn-glycerol in water (Lindblom et al. 1993. J. Biol. Chem. 268:16198-16207). The phase behavior of the two lipids suggests that hydrophobic substitution of a hydroxyl group in the sugar ring of the glucopyranosylglycerols has a very strong effect on their physicochemical properties, i.e., headgroup hydration and the formation of different lipid aggregate structures. PMID:7811919

  7. Does dynamic vulcanization induce phase separation?

    PubMed

    Abolhasani, Mohammad Mahdi; Zarejousheghani, Fatemeh; Naebe, Minoo; Guo, Qipeng

    2014-08-14

    Immiscible and miscible blends of poly(vinylidene fluoride) (PVDF) and acrylic rubber (ACM) were subjected to dynamic vulcanization to investigate the effect of crosslinking on phase separation. As a result of different processability, mixing torque behavior of miscible and immiscible blends was significantly different from one another. Scanning electron microscopy (SEM) was used to investigate the morphology of the system. After dynamic vulcanization, submicron ACM droplets were observed in the samples near the binodal curve of the system under mixing conditions. Small angle X-ray scattering (SAXS) and differential scanning calorimetry (DSC) analysis were used to investigate the effect of dynamic vulcanization on the lamellar structure of the system. It was shown that for samples near the boundary of phase separation, increasing the crosslink density led to a decrease in the lamellar long period (L) as a sign of increment of crosslink density induced phase decomposition. Effects of shear rate on the final morphology of the system were investigated by changing the mixing temperature and by comparing the results of dynamic vulcanization at one phase and two phase regions.

  8. Thermocapillary-Induced Phase Separation with Coalescence

    NASA Technical Reports Server (NTRS)

    Davis, Robert H.

    2003-01-01

    Research has been undertaken on interactions of two or more deformable drops (or bubbles) in a viscous fluid and subject to a temperature, gravitational, or flow field. An asymptotic theory for nearly spherical drops shows that small deformations reduce the coalescence and phase separation rates. Boundary-integral simulations for large deformations show that bubbles experience alignment and enhanced coalescence, whereas more viscous drops may break as a result of hydrodynamic interactions. Experiments for buoyancy motion confirm these observations. Simulations of the sedimentation of many drops show clustering phenomena due to deformations, which lead to enhanced phase separation rates, and simulations of sheared emulsions show that deformations cause a reduction in the effective viscosity.

  9. Simualting the Phase Separated rp-ash

    NASA Astrophysics Data System (ADS)

    Caplan, Matthew; Horowitz, Chuck; Berry, Donald

    2017-01-01

    The composition and phase separation of rp-ash on accreting neutron stars determine the thermal properties of the crust which must be understood to interpret observations of crust cooling in X-ray bursts. In this work, we report on recent large scale molecular dynamics simulations of the outer crust. Using the crust compositions calculated by Mckinven et al. 2016, we study the structure of the crystal that forms, as well as diffusion and thermal properties of the crust.

  10. Phase separation kinetics in immiscible liquids

    NASA Technical Reports Server (NTRS)

    Ng, Lee H.; Sadoway, Donald R.

    1987-01-01

    The kinetics of phase separation in the succinonitrile-water system are being investigated. Experiments involve initial physical mixing of the two immiscible liquids at a temperature above the consolute, decreasing the temperature into the miscibility gap, followed by iamging of the resultant microstructure as it evolves with time. Refractive index differences allow documentation of the changing microstructures by noninvasive optical techniques without the need to quench the liquid structures for analysis.

  11. Phase separation kinetics in immiscible liquids

    NASA Technical Reports Server (NTRS)

    Sadoway, D. R.

    1986-01-01

    The kinetics of phase separation in the succinonitrile-water system are being investigated. Experiments involve initial physical mixing of the two immiscible liquids at a temperature above the consolute, decreasing the temperature into the miscibility gap, followed by imaging of the resultant microstructure as it evolves with time. Refractive index differences allow documentation of the changing microstructures by noninvasive optical techniques without the need to quench the liquid structures for analysis.

  12. Wetting and phase separation in soft adhesion

    PubMed Central

    Jensen, Katharine E.; Sarfati, Raphael; Style, Robert W.; Boltyanskiy, Rostislav; Chakrabarti, Aditi; Chaudhury, Manoj K.; Dufresne, Eric R.

    2015-01-01

    In the classic theory of solid adhesion, surface energy drives deformation to increase contact area whereas bulk elasticity opposes it. Recently, solid surface stress has been shown also to play an important role in opposing deformation of soft materials. This suggests that the contact line in soft adhesion should mimic that of a liquid droplet, with a contact angle determined by surface tensions. Consistent with this hypothesis, we observe a contact angle of a soft silicone substrate on rigid silica spheres that depends on the surface functionalization but not the sphere size. However, to satisfy this wetting condition without a divergent elastic stress, the gel phase separates from its solvent near the contact line. This creates a four-phase contact zone with two additional contact lines hidden below the surface of the substrate. Whereas the geometries of these contact lines are independent of the size of the sphere, the volume of the phase-separated region is not, but rather depends on the indentation volume. These results indicate that theories of adhesion of soft gels need to account for both the compressibility of the gel network and a nonzero surface stress between the gel and its solvent. PMID:26553989

  13. Active Nematics Are Intrinsically Phase Separated

    NASA Astrophysics Data System (ADS)

    Mishra, Shradha; Ramaswamy, Sriram

    2006-09-01

    Two-dimensional nonequilibrium nematic steady states, as found in agitated granular-rod monolayers or films of orientable amoeboid cells, were predicted [Europhys. Lett. 62, 196 (2003)EULEEJ0295-507510.1209/epl/i2003-00346-7] to have giant number fluctuations, with the standard deviation proportional to the mean. We show numerically that the steady state of such systems is macroscopically phase separated, yet dominated by fluctuations, as in the Das-Barma model [Phys. Rev. Lett. 85, 1602 (2000)PRLTAO0031-900710.1103/PhysRevLett.85.1602]. We suggest experimental tests of our findings in granular and living-cell systems.

  14. Porous polymers by controlling phase separation during vapor deposition polymerization.

    PubMed

    Tao, Ran; Anthamatten, Mitchell

    2013-11-01

    A template-free method is described to fabricate continuous-phase, porous polymer films by simultaneous phase separation during vapor deposition polymerization. The technique involves concurrent polymerization, crosslinking, and phase separation of condensed species and reaction products. Deposited films form open-cell, macroporous structures consisting of crosslinked and glassy poly(glycidyl methacrylate). By limiting phase separation during vapor phase deposition, spatially dependent morphologies, such as layered morphologies, can be grown. Results show that combining vapor deposition polymerization with phase separation establishes morphological control, which may be applied to applications including cellular scaffolds, thin cushions and vibration dampers, and membranes for separations.

  15. Griffiths phase and temporal effects in phase separated manganites

    NASA Astrophysics Data System (ADS)

    Krivoruchko, V. N.; Marchenko, M. A.

    2016-08-01

    Phenomenological description of relaxation phenomena in magnetic and transport properties of perovskite manganites has been presented. The approach is based on generalization of some hypotheses appropriate to the Preisach picture of magnetization process for half-metallic ferromagnets and on an assumption that in doped manganites the phase separated state exists near the magnetic ordering temperature. For systems with the percolation type of a ferromagnet-paramagnet transition, distinctive features in relaxation of magnetization and resistivity have been found. The relaxation is shown to be most pronounced near the transition temperature, and to be an approximately logarithmic function of time. The theoretical results replicate a broad spectrum of behavior observed experimentally on time dependence of magnetization and resistivity of CMR systems and allow a direct comparison with available experimental data. We propose an additional experimental test to distinguish between the percolation scenario of magnetic and transport transitions in doped manganites, and the ferromagnetic polaron picture. In particular, an anomalously slow relaxation to zero of the order parameter can be considered as a key feature of the Griffiths-like phase transition in doped manganites. It is also shown that a system with the Griffiths-like state will exhibit nonequilibrium aging and rejuvenation phenomena, which in many aspects resemble that of a spin glass. We hope that experimental observation of a set of time decay properties will provide a settlement of apparently conflicting results obtained for different characteristics of phase-separated manganites.

  16. Carbon nanotubes in thermotropic low molar mass liquid crystals

    NASA Astrophysics Data System (ADS)

    Schymura, Stefan; Park, Ji Hyun; Dierking, Ingo; Scalia, Giusy

    Carbon nanotubes constitute a highly anisotropic form of carbon with outstanding mechanical, thermal and electrical properties. Their dispersion and organization are important but challenging and this chapter describes the advantages of using thermotropic liquid crystals as host for nanotube dispersion and ordering. The self organization of LCs is an attractive way to manipulate nanoparticles such as carbon nanotubes or graphene akes. Compared to standard carbon nanotube composites (e.g. with disordered polymer hosts) the introduction of the nanotubes into an LC allows not only the transfer of the outstanding nanotube properties to the oscopic phase, providing strength and conductivity, but these properties also become anisotropic, following the transfer of the orientational order from the LC to the CNTs...

  17. The Kinetics of Phase Separation in Asymmetric Membranes

    PubMed Central

    Wallace, Elizabeth J.; Hooper, Nigel M.; Olmsted, Peter D.

    2005-01-01

    Phase separation in a model asymmetric membrane is studied using Monte Carlo techniques. The membrane comprises two species of particles, which mimic different lipids in lipid bilayers and separately possess either zero or non-zero spontaneous curvatures. We study the influence of phase separation on membrane shape and the influence of the coupling of composition and height dynamics on phase separation and domain growth, via both the degree of shape asymmetry and relative kinetic coefficients for height relaxation. PMID:15778446

  18. Strain phase separation: Formation of ferroelastic domain structures

    NASA Astrophysics Data System (ADS)

    Xue, Fei; Li, Yongjun; Gu, Yijia; Zhang, Jinxing; Chen, Long-Qing

    2016-12-01

    Phase decomposition is a well-known process leading to the formation of two-phase mixtures. Here we show that a strain imposed on a ferroelastic crystal promotes the formation of mixed phases and domains, i.e., strain phase separation with local strains determined by a common tangent construction on the free energy versus strain curves. It is demonstrated that a domain structure can be understood using the concepts of domain/phase rule, lever rule, and coherent and incoherent strain phase separation, in a complete analogy to phase decomposition. The proposed strain phase separation model is validated using phase-field simulations and experimental observations of PbTi O3 and BiFe O3 thin films as examples. The proposed model provides a simple tool to guide and design domain structures of ferroelastic systems.

  19. Toughening Thermoplastics with Thermotropic Liquid Crystal Polymers

    NASA Astrophysics Data System (ADS)

    Wiff, Donald

    1997-03-01

    Blends of thermotropic liquid crystalline and thermoplastic polymers have improvements in mechanical properties when high elongational flow provides LC needle shaped domains. This means the test sample must be a filament. Without elongational flow the LC domains are globular in shape and provide little or no mechanical property enhancement. One solution to this problem is to make the LC domains small enough so that their size approaches that of microvoids in the thermoplastic polymer system. Such an approach can potentially provide a pseudo-compatible blend. Thus if the thermoplastic matrix polymer is transparent, the nano size LC domains can provide reinforcement, modified optical properties, and still leave the bulk material transparent. This investigation focusses on the process and improvement in mechanical and fracture resistant properties.

  20. Superfluid helium 2 liquid-vapor phase separation: Technology assessment

    NASA Technical Reports Server (NTRS)

    Lee, J. M.

    1984-01-01

    A literature survey of helium 2 liquid vapor phase separation is presented. Currently, two types of He 2 phase separators are being investigated: porous, sintered metal plugs and the active phase separator. The permeability K(P) shows consistency in porous plug geometric characterization. Both the heat and mass fluxes increase with K(P). Downstream pressure regulation to adjust for varying heat loads and both temperatures is possible. For large dynamic heat loads, the active phase separator shows a maximum heat rejection rate of up to 2 W and bath temperature stability of 0.1 mK. Porous plug phase separation performance should be investigated for application to SIRTF and, in particular, that plugs of from 10 to the minus ninth square centimeters to 10 to the minus eighth square centimeters in conjunction with downstream pressure regulation be studied.

  1. Thermotropic behavior of poly(oxyethylene) cholesterol ethers.

    PubMed

    López-Quintela, M Arturo; Akahane, Akira; Rodríguez, Carlos; Kunieda, Hironobu

    2002-03-01

    The thermotropic behavior of poly(oxyethylene) cholesterol ether surfactants was studied by differential scanning calorimetry and small-angle X-ray scattering. Contrary to what is usually observed in conventional poly(oxyethylene)-type surfactant systems, poly(oxyethylene) cholesterol ether surfactants show a change of the fusion mechanism as the chain length is varied. For long chain lengths (n > or = 15) the usual solid-liquid transition is found, but for short chain lengths (n < or = 10) the transition goes through a birefringent lamellar phase. The appearance of this liquid crystal (LC) phase seems to be related with the predominance of the cholesterol part in the short chain polyoxyethylene surfactants. On the contrary, for long polyexyethylene chains the polymer gains in importance and only a solid crystalline structure is observed at low temperatures. An antiparallel packing structure with totally overlapped chains is found for both, the solid and the LC phase. The chains seem to be in a zigzag configuration, and only for the longest surfactant here studied (n = 30) a change of the chain configuration to a much shorter meander configuration is observed.

  2. Sequence-Specific Polyampholyte Phase Separation in Membraneless Organelles

    NASA Astrophysics Data System (ADS)

    Lin, Yi-Hsuan; Forman-Kay, Julie D.; Chan, Hue Sun

    2016-10-01

    Liquid-liquid phase separation of charge- and/or aromatic-enriched intrinsically disordered proteins (IDPs) is critical in the biological function of membraneless organelles. Much of the physics of this recent discovery remains to be elucidated. Here, we present a theory in the random phase approximation to account for electrostatic effects in polyampholyte phase separations, yielding predictions consistent with recent experiments on the IDP Ddx4. The theory is applicable to any charge pattern and thus provides a general analytical framework for studying sequence dependence of IDP phase separation.

  3. SEC/reversed-phase separation of E. coli proteins.

    PubMed

    Apffell, Alex

    2010-05-01

    Although many chromatographic modes can be coupled for the multidimensional separation of a complex mixture, a very favorable combination is that of size-exclusion chromatography (SEC) and reversed-phase chromatography. The separation mechanisms are largely orthogonal and the mobile phases are compatible. The use of a retentive second dimension allows trapping of specific fractions from the SEC separation and transferring them to the reversed-phase separation. One of the advantages of multidimensional chromatography is that it is scalable in terms of automation. In a completely manual system, fractions eluting from a first dimension can be manually collected and injected into a second separation dimension. In an automated system, fraction transfer can be accomplished through automated valving. The following protocol illustrates this approach, with both a manual method and an external column switching method integrated into an automated high-performance liquid chromatography (HPLC) method. As an illustration, soluble proteins from Escherichia coli are separated.

  4. Continuum Theory of Phase Separation Kinetics for Active Brownian Particles

    NASA Astrophysics Data System (ADS)

    Stenhammar, Joakim; Tiribocchi, Adriano; Allen, Rosalind J.; Marenduzzo, Davide; Cates, Michael E.

    2013-10-01

    Active Brownian particles (ABPs), when subject to purely repulsive interactions, are known to undergo activity-induced phase separation broadly resembling an equilibrium (attraction-induced) gas-liquid coexistence. Here we present an accurate continuum theory for the dynamics of phase-separating ABPs, derived by direct coarse graining, capturing leading-order density gradient terms alongside an effective bulk free energy. Such gradient terms do not obey detailed balance; yet we find coarsening dynamics closely resembling that of equilibrium phase separation. Our continuum theory is numerically compared to large-scale direct simulations of ABPs and accurately accounts for domain growth kinetics, domain topologies, and coexistence densities.

  5. Phase Separators And Fountain-Effect Pumps For He 11

    NASA Technical Reports Server (NTRS)

    Whitehouse, Paul L.

    1989-01-01

    Fused-glass microchannel arrays for use as HE 11 phase separators and fountain-effect pumps. Microchannel devices for use in low-gravity storage and cooling systems containing superfluid helium. Phase separators and pumps take advantage of thermomechanical effect peculiar to He 11 in restricted spaces. By creating thermal gradient in porous plug, direction of flow reversed, turning phase separator into pump. However, addition of heat disadvantage. Thermal gradient created by using Peltier effect to transfer heat across array, removing heat from He 11 supply and overcoming undesirable addition of heat.

  6. Crystalline structure and thermotropic behavior of alkyltrimethylphosphonium amphiphiles.

    PubMed

    Gamarra, Ana; Urpí, Lourdes; Martínez de Ilarduya, Antxon; Muñoz-Guerra, Sebastián

    2017-02-08

    Quaternary organophosphonium salts bearing long alkyl chains are cationic surfactants of interest owing to their physical and biological properties. In the present work, the crystal structure and thermotropic behavior of the homologous series of alkyltrimethylphosphonium bromides (nATMP·Br), with the alkyl chain containing an even number (n) of carbon atoms from 12 to 22, have been examined within the 0-300 °C range of temperatures. These compounds were shown to be resistant to heat up to ∼390 °C. The phases adopted at different temperatures were detected by DSC, and the structural changes involved in the phase transitions have been characterized by simultaneous WAXS and SAXS carried out in real-time, and by polarizing optical microscopy as well. Three or four phases were identified for n = 12 and 14 or n ≥ 16, respectively, in agreement with the heat exchange peaks observed by DSC. The phase existing at room temperature (Ph-I) was found to be fully crystalline and its crystal lattice was determined by single-crystal X-ray diffraction methods. Ph-II consisted of a semicrystalline structure that can be categorized as Smectic-B with the crystallized ionic pairs hexagonally arranged in layers and the molten alkyl chain confined in the interlayer space. Ph-II of 12ATMP·Br and 14ATMP·Br directly isotropicized upon heating at ∼220 °C, whereas for n ≥ 16, it converted into a Smectic-A phase (Ph-III) that needed to be heated above ∼240 °C to become isotropic (Ph-Is). The correlation existing between the thermal behavior, phase structure and length of the alkyl side chain has been demonstrated.

  7. Phase separation and the formation of cellular bodies

    NASA Astrophysics Data System (ADS)

    Xu, Bin; Broedersz, Chase P.; Meir, Yigal; Wingreen, Ned S.

    Cellular bodies in eukaryotic cells spontaneously assemble to form cellular compartments. Among other functions, these bodies carry out essential biochemical reactions. Cellular bodies form micron-sized structures, which, unlike canonical cell organelles, are not surrounded by membranes. A recent in vitro experiment has shown that phase separation of polymers in solution can explain the formation of cellular bodies. We constructed a lattice-polymer model to capture the essential mechanism leading to this phase separation. We used both analytical and numerical tools to predict the phase diagram of a system of two interacting polymers, including the concentration of each polymer type in the condensed and dilute phase.

  8. Phase separation in the isolation and purification of membrane proteins.

    PubMed

    Arnold, Thomas; Linke, Dirk

    2007-10-01

    Phase separation is a simple, efficient, and cheap method to purify and concentrate detergent-solubilized membrane proteins. In spite of this, phase separation is not widely used or even known among membrane protein scientists, and ready-to-use protocols are available for only relatively few detergent/membrane protein combinations. Here, we summarize the physical and chemical parameters that influence the phase separation behavior of detergents commonly used for membrane protein studies. Examples for the successful purification of membrane proteins using this method with different classes of detergents are provided. As the choice of the detergent is critical in many downstream applications (e.g., membrane protein crystallization or functional assays), we discuss how new phase separation protocols can be developed for a given detergent buffer system.

  9. Separation of Chloroplast Pigments Using Reverse Phase Chromatography.

    ERIC Educational Resources Information Center

    Reese, R. Neil

    1997-01-01

    Presents a protocol that uses reverse phase chromatography for the separation of chloroplast pigments. Provides a simple and relatively safe procedure for use in teaching laboratories. Discusses pigment extraction, chromatography, results, and advantages of the process. (JRH)

  10. Thermotropic and lyotropic behaviour of new liquid-crystalline materials with different hydrophilic groups: synthesis and mesomorphic properties

    PubMed Central

    Kašpar, Miroslav; Hamplová, Věra; Dawin, Ute; Giesselmann, Frank

    2013-01-01

    Summary Several new calamitic liquid-crystalline (LC) materials with flexible hydrophilic chains, namely either hydroxy groups or ethylene glycol units, or both types together, have been synthesized in order to look for new functional LC materials exhibiting both, thermotropic and lyotropic behaviour. Such materials are of high potential interest for challenging issues such as the self-organization of carbon nanotubes or various nanoparticles. Thermotropic mesomorphic properties have been studied by using polarizing optical microscopy, differential scanning calorimetry and X-ray scattering. Four of these nonchiral and chiral materials exhibit nematic and chiral nematic phases, respectively. For some molecular structures, smectic phases have also been detected. A contact sample of one of the prepared compounds with diethylene glycol clearly shows the lyotropic behaviour; namely a lamellar phase was observed. The relationship between the molecular structure and mesomorphic properties of these new LCs with hydrophilic chains is discussed. PMID:23504455

  11. Thermotropic and lyotropic behaviour of new liquid-crystalline materials with different hydrophilic groups: synthesis and mesomorphic properties.

    PubMed

    Bubnov, Alexej; Kašpar, Miroslav; Hamplová, Věra; Dawin, Ute; Giesselmann, Frank

    2013-01-01

    Several new calamitic liquid-crystalline (LC) materials with flexible hydrophilic chains, namely either hydroxy groups or ethylene glycol units, or both types together, have been synthesized in order to look for new functional LC materials exhibiting both, thermotropic and lyotropic behaviour. Such materials are of high potential interest for challenging issues such as the self-organization of carbon nanotubes or various nanoparticles. Thermotropic mesomorphic properties have been studied by using polarizing optical microscopy, differential scanning calorimetry and X-ray scattering. Four of these nonchiral and chiral materials exhibit nematic and chiral nematic phases, respectively. For some molecular structures, smectic phases have also been detected. A contact sample of one of the prepared compounds with diethylene glycol clearly shows the lyotropic behaviour; namely a lamellar phase was observed. The relationship between the molecular structure and mesomorphic properties of these new LCs with hydrophilic chains is discussed.

  12. Phase-Locked Semiconductor Lasers With Separate Contacts

    NASA Technical Reports Server (NTRS)

    Katz, Joseph; Yariv, Amnon; Margalit, Shlomo

    1988-01-01

    Individual current feeds enable better uniformity and flexible control. Separate contacts for lasers in array enable control of output radiation pattern and compensation of manufacturing nonuniformities among lasers. Concept of separate current control described for two-laser array in "Semiconductor Laser Phased Array" (NPO-15963).

  13. Probe diffusion in phase-separated bicontinuous biopolymer gels.

    PubMed

    Wassén, Sophia; Bordes, Romain; Gebäck, Tobias; Bernin, Diana; Schuster, Erich; Lorén, Niklas; Hermansson, Anne-Marie

    2014-11-07

    Probe diffusion was determined in phase separated bicontinuous gels prepared by acid-induced gelation of the whey protein isolate-gellan gum system. The topological characterization of the phase-separated gel systems is achieved by confocal microscopy and the diffusion measurements are performed using pulsed field gradient (PFG) NMR and fluorescence recovery after photo-bleaching (FRAP). These two techniques gave complementary information about the mass transport at different time- and length scales, PFG NMR provided global diffusion rates in the gel systems, while FRAP enabled the measurements of diffusion in different phases of the phase-separated gels. The results revealed that the phase-separated gel with the largest characteristic wavelength had the fastest diffusion coefficient, while the gel with smaller microstructures had a slower probe diffusion rate. By using the diffusion data obtained by FRAP and the structural data from confocal microscopy, modelling through the lattice-Boltzmann framework was carried out to simulate the global diffusion and verify the validity of the experimental measurements. With this approach it was found that discrepancies between the two experimental techniques can be rationalized in terms of probe distribution between the different phases of the system. The combination of different techniques allowed the determination of diffusion in a phase-separated biopolymer gel and gave a clearer picture of this complex system. We also illustrate the difficulties that can arise if precautions are not taken to understand the system-probe interactions.

  14. Thermotropic nematic order upon nanocapillary filling

    NASA Astrophysics Data System (ADS)

    Huber, Patrick; Busch, Mark; Całus, Sylwia; Kityk, Andriy V.

    2013-04-01

    Optical birefringence and light absorption measurements reveal four regimes for the thermotropic behavior of a nematogen liquid (7CB) upon sequential filling of parallel-aligned capillaries of 12 nm diameter in a monolithic, mesoporous silica membrane. No molecular reorientation is observed for the first adsorbed monolayer. In the film-condensed state (up to 1 nm thickness), a weak, continuous paranematic-to-nematic (P-N) transition is found, which is shifted by 10 K below the discontinuous bulk transition at TIN=305 K. The capillary-condensed state exhibits a more pronounced, albeit still continuous P-N reordering, located 4 K below TIN. This shift vanishes abruptly upon complete filling of the capillaries. It could originate in competing anchoring conditions at the free inner surfaces and at the pore walls or result from the 10-MPa tensile pressure release associated with the disappearance of concave menisci in the confined liquid upon complete filling. The study documents that the thermo-optical properties of nanoporous systems (or single nanocapillaries) can be tailored over a surprisingly wide range simply by variation of the filling fraction with liquid crystals.

  15. Separate Magnitude and Phase Regularization via Compressed Sensing

    PubMed Central

    Noll, Douglas C.; Nielsen, Jon-Fredrik; Fessler, Jeffrey A.

    2012-01-01

    Compressed sensing (CS) has been used for accelerating magnetic resonance imaging (MRI) acquisitions, but its use in applications with rapid spatial phase variations is challenging, e.g., proton resonance frequency shift (PRF-shift) thermometry and velocity mapping. Previously, an iterative MRI reconstruction with separate magnitude and phase regularization was proposed for applications where magnitude and phase maps are both of interest, but it requires fully sampled data and unwrapped phase maps. In this paper, CS is combined into this framework to reconstruct magnitude and phase images accurately from undersampled data. Moreover, new phase regularization terms are proposed to accommodate phase wrapping and to reconstruct images with encoded phase variations, e.g., PRF-shift thermometry and velocity mapping. The proposed method is demonstrated with simulated thermometry data and in-vivo velocity mapping data and compared to conventional phase corrected CS. PMID:22552571

  16. Texas A&M vortex type phase separator

    NASA Astrophysics Data System (ADS)

    Best, Frederick

    2000-01-01

    Phase separation is required for regenerative biological and chemical process systems as well as thermal transport and rejection systems. Liquid and gas management requirements for future spacecraft will demand small, passive systems able to operate over wide ranges of inlet qualities. Conservation and recycling of air and water is a necessary part of the construction and operation of the International Space Station as well as future long duration space missions. Space systems are sensitive to volume, mass, and power. Therefore, it is necessary to develop a method to recycle wastewater with minimal power consumption. Regenerative life support systems currently being investigated require phase separation to separate the liquid from the gas produced. The microgravity phase separator designed and fabricated at Texas A&M University relies on centripetal driven buoyancy forces to form a gas-liquid vortex within a fixed, right-circular cylinder. Two-phase flow is injected tangentially along the inner wall of this cylinder producing a radial acceleration gradient. The gradient produced from the intrinsic momentum of the injected mixture results in a rotating flow that drives the buoyancy process by the production of a hydrostatic pressure gradient. Texas A&M has flown several KC-135 flights with separator. These flights have included scaling studies, stability and transient investigations, and tests for inventory instrumentation. Among the hardware tested have been passive devices for separating mixed vapor/liquid streams into single-phase streams of vapor only and liquid only. .

  17. Chromatographic Separations Using Solid-Phase Extraction Cartridges: Separation of Wine Phenolics

    NASA Astrophysics Data System (ADS)

    Brenneman, Charles A.; Ebeler, Susan E.

    1999-12-01

    We describe a simple laboratory experiment that demonstrates the principles of chromatographic separation using solid-phase extraction columns and red wine. By adjusting pH and mobile phase composition, the wine is separated into three fractions of differing polarity. The content of each fraction can be monitored by UV-vis spectroscopy. When the experiment is combined with experiments involving HPLC or GC separations, students gain a greater appreciation for and understanding of the highly automated instrumental systems currently available. In addition, they learn about the chemistry of polyphenolic compounds, which are present in many foods and beverages and which are receiving much attention for their potentially beneficial health effects.

  18. Laser-induced phase separation of silicon carbide.

    PubMed

    Choi, Insung; Jeong, Hu Young; Shin, Hyeyoung; Kang, Gyeongwon; Byun, Myunghwan; Kim, Hyungjun; Chitu, Adrian M; Im, James S; Ruoff, Rodney S; Choi, Sung-Yool; Lee, Keon Jae

    2016-11-30

    Understanding the phase separation mechanism of solid-state binary compounds induced by laser-material interaction is a challenge because of the complexity of the compound materials and short processing times. Here we present xenon chloride excimer laser-induced melt-mediated phase separation and surface reconstruction of single-crystal silicon carbide and study this process by high-resolution transmission electron microscopy and a time-resolved reflectance method. A single-pulse laser irradiation triggers melting of the silicon carbide surface, resulting in a phase separation into a disordered carbon layer with partially graphitic domains (∼2.5 nm) and polycrystalline silicon (∼5 nm). Additional pulse irradiations cause sublimation of only the separated silicon element and subsequent transformation of the disordered carbon layer into multilayer graphene. The results demonstrate viability of synthesizing ultra-thin nanomaterials by the decomposition of a binary system.

  19. Laser-induced phase separation of silicon carbide

    PubMed Central

    Choi, Insung; Jeong, Hu Young; Shin, Hyeyoung; Kang, Gyeongwon; Byun, Myunghwan; Kim, Hyungjun; Chitu, Adrian M.; Im, James S.; Ruoff, Rodney S.; Choi, Sung-Yool; Lee, Keon Jae

    2016-01-01

    Understanding the phase separation mechanism of solid-state binary compounds induced by laser–material interaction is a challenge because of the complexity of the compound materials and short processing times. Here we present xenon chloride excimer laser-induced melt-mediated phase separation and surface reconstruction of single-crystal silicon carbide and study this process by high-resolution transmission electron microscopy and a time-resolved reflectance method. A single-pulse laser irradiation triggers melting of the silicon carbide surface, resulting in a phase separation into a disordered carbon layer with partially graphitic domains (∼2.5 nm) and polycrystalline silicon (∼5 nm). Additional pulse irradiations cause sublimation of only the separated silicon element and subsequent transformation of the disordered carbon layer into multilayer graphene. The results demonstrate viability of synthesizing ultra-thin nanomaterials by the decomposition of a binary system. PMID:27901015

  20. Laser-induced phase separation of silicon carbide

    NASA Astrophysics Data System (ADS)

    Choi, Insung; Jeong, Hu Young; Shin, Hyeyoung; Kang, Gyeongwon; Byun, Myunghwan; Kim, Hyungjun; Chitu, Adrian M.; Im, James S.; Ruoff, Rodney S.; Choi, Sung-Yool; Lee, Keon Jae

    2016-11-01

    Understanding the phase separation mechanism of solid-state binary compounds induced by laser-material interaction is a challenge because of the complexity of the compound materials and short processing times. Here we present xenon chloride excimer laser-induced melt-mediated phase separation and surface reconstruction of single-crystal silicon carbide and study this process by high-resolution transmission electron microscopy and a time-resolved reflectance method. A single-pulse laser irradiation triggers melting of the silicon carbide surface, resulting in a phase separation into a disordered carbon layer with partially graphitic domains (~2.5 nm) and polycrystalline silicon (~5 nm). Additional pulse irradiations cause sublimation of only the separated silicon element and subsequent transformation of the disordered carbon layer into multilayer graphene. The results demonstrate viability of synthesizing ultra-thin nanomaterials by the decomposition of a binary system.

  1. Degree of disorder in cubic mesophases in thermotropics: thermodynamic study of a liquid crystal showing two cubic mesophases.

    PubMed

    Saito, Kazuya; Shinhara, Takashi; Nakamoto, Tadahiro; Kutsumizu, Shoichi; Yano, S; Sorai, Michio

    2002-03-01

    Heat capacity of a thermotropic mesogen ANBC(22) (4(')-alkoxy-3(')-nitrobiphenyl-4-carboxylic acid with 22 carbon atoms in alkyl chain) showing two cubic mesophases was measured by adiabatic calorimetry between 13 and 480 K. Excess enthalpies and entropies due to phase transitions were determined. A small thermal anomaly due to the cubic Im3m-->cubic Ia3d phase transition was successfully detected. Through an analysis of chain-length dependence of the entropy of transition, the sequence of two cubic mesophases (with space groups Ia3d and Im3m) is deduced for thermotropic mesogens ANBC(n). It is shown that the disorder of the core arrangement decreases in the order of Sm-C-->cubic (Im3m)-->cubic (Ia3d) while that of the chain in the reverse order cubic (Ia3d)-->cubic (Im3m)-->Sm C.

  2. Phase separation of lanthanum hydride under high pressure

    NASA Astrophysics Data System (ADS)

    Machida, A.; Watanuki, T.; Kawana, D.; Aoki, K.

    2011-02-01

    Structural change of lanthanum dihydride LaH2.3, which has a face-centered-cubic (fcc) metal lattice with tetrahedral interstitial sites fully occupied with hydrogen atoms and partially occupied octahedral sites, has been investigated at high pressures up to 20 GPa at ambient temperature by synchrotron radiation x-ray diffraction. Additional Bragg reflections appear just on higher angle sides of the original ones at ~11 GPa and their peak intensities increase gradually on further compression. The coexistence state of two fcc metal lattices thus observed above 11 GPa is interpreted in terms of phase separation or disproportionation reaction from the dihydride toward a solid solution and trihydride states, in both of which the octahedral interstitial sites are partially occupied with hydrogen atoms. A gradual distortion from the cubic to a tetragonal lattice is observed prior to the phase separation. The coexistence phase goes back to the dihydride fcc phase via the lattice distorted phase with decreasing pressure.

  3. Gas Phase Chiral Separations By Ion Mobility Spectrometry

    PubMed Central

    Dwivedi, Prabha; Wu, Ching; Hill, Herbert H.

    2013-01-01

    This manuscript introduces the concept of Chiral Ion Mobility Spectrometry (CIMS) and presents examples demonstrating the gas phase separation of enantiomers of a wide range of racemates including pharmaceuticals, amino acids and carbohydrates. CIMS is similar to traditional ion mobility spectrometry (IMS), where gas phase ions, when subjected to a potential gradient are separated at atmospheric pressure due to differences in their shapes and sizes. In addition to size and shape, CIMS separates ions based on their stereospecific interaction with a chiral gas. In order to achieve chiral discrimination by CIMS, an asymmetric environment was provided by doping the drift gas with a volatile chiral reagent. In this study S-(+)-2-butanol was used as a chiral modifier to demonstrate enantiomeric separations of atenolol, serine, methionine, threonine, methyl-α-glucopyranoside, glucose, penicillamine, valinol, phenylalanine, and tryptophan from their respective racemic mixtures. PMID:17165808

  4. Phase separation during radiation crosslinking of unsaturated polyester resin

    NASA Astrophysics Data System (ADS)

    Pucić, Irina; Ranogajec, Franjo

    2003-06-01

    Phase separation during radiation-initiated crosslinking of unsaturated polyester resin was studied. Residual reactivity of liquid phases and gels of partially cured samples was determined by DSC. Uncured resin and liquid phases showed double reaction exotherm, gels had a single maximum that corresponded to higher-temperature maximum of liquid parts. The lower-temperature process was attributed to styrene-polyester copolymerization. At higher temperatures, polyester unsaturations that remained unreacted due to microgel formation homopolymerized. FTIR revealed different composition of phases. In thicker samples, reaction heat influenced microgel formation causing delayed appearance of gel and faster increase in conversion.

  5. Supercritical fluid phase separations induced by chemical reactions

    SciTech Connect

    Ree, F.H.; Viecelli, J.A.; van Thiel, M.

    1997-11-01

    Our statistical mechanical studies predict that a chemically reactive system containing species composed of C, H, N, O atoms can exhibit a phase separation into a N{sub 2}-rich and a N{sub 2}-poor phase. The preset work is concerned with the effect of the fluid phase separation upon addition of F atoms in the system. Our study shows that F atoms mainly appear as a constituent of HF in a N{sub 2}-poor fluid phase up to a certain pressure beyond which they occur as CF{sub 4} in a N{sub 2}-rich phase and that the phase separation may be abrupt in thermodynamic sense. The pressure at the phase boundary can occur at about 30 GPa at 3000 K and about 10 GPa to 20 GPa at 1000 K.Some of these ranges maybe accessible by present-day experimental high-pressure techniques. We discuss implications of this study to detonation physics.

  6. Phase separation in biological membranes: integration of theory and experiment

    PubMed Central

    Elson, Elliot L.; Fried, Eliot; Dolbow, John E.; Genin, Guy M.

    2013-01-01

    Lipid bilayer model membranes can undergo transitions between ordered and disordered phases, and membranes that contain a mixture of lipid species can undergo phase separations. Studies of these transformations are of interest for what they can tell us about the interaction energies of lipid molecules of different species and conformations. Nanoscopic phases can provide a model for membrane rafts, which have important biological functions in cell membranes. Important questions are whether lipid nanodomains can exist in stable equilibrium in membranes and what is the distribution of their sizes in membranes of different composition. It is also important to know the lifetimes of nanodomains. Theoretical methods have supplied much important information on these questions, but better experimental methods are needed to detect and characterize nanodomains under normal membrane conditions. This review summarizes linkages between theoretical and experimental studies of phase separation in lipid bilayer model membranes. PMID:20192775

  7. Phase separation in biological membranes: integration of theory and experiment.

    PubMed

    Elson, Elliot L; Fried, Eliot; Dolbow, John E; Genin, Guy M

    2010-01-01

    Lipid bilayer model membranes that contain a single lipid species can undergo transitions between ordered and disordered phases, and membranes that contain a mixture of lipid species can undergo phase separations. Studies of these transformations are of interest for what they can tell us about the interaction energies of lipid molecules of different species and conformations. Nanoscopic phases (<200 nm) can provide a model for membrane rafts, specialized membrane domains enriched in cholesterol and sphingomyelin, which are believed to have essential biological functions in cell membranes. Crucial questions are whether lipid nanodomains can exist in stable equilibrium in membranes and what is the distribution of their sizes and lifetimes in membranes of different composition. Theoretical methods have supplied much information on these questions, but better experimental methods are needed to detect and characterize nanodomains under normal membrane conditions. This review summarizes linkages between theoretical and experimental studies of phase separation in lipid bilayer model membranes.

  8. Phase Separation kinetics in an Fe-Cr-Al alloy

    SciTech Connect

    Capdevila, C.; Miller, Michael K; Chao, J.

    2012-01-01

    The {alpha}-{alpha}{prime} phase separation kinetics in a commercial Fe-20 wt.% Cr-6 wt.% Al oxide dispersion-strengthened PM 2000{trademark} steel have been characterized with the complementary techniques atom probe tomography and thermoelectric power measurements during isothermal aging at 673, 708, and 748 K for times up to 3600 h. A progressive decrease in the Al content of the Cr-rich {alpha}{prime} phase was observed at 708 and 748 K with increasing time, but no partitioning was observed at 673 K. The variation in the volume fraction of the {alpha}{prime} phase well inside the coarsening regime, along with the Avrami exponent 1.2 and activation energy 264 kJ mol{sup -1}, obtained after fitting the experimental results to an Austin-Rickett type equation, indicates that phase separation in PM 2000{trademark} is a transient coarsening process with overlapping nucleation, growth, and coarsening stages.

  9. DUAL PHASE MEMBRANE FOR HIGH TEMPERATURE CO2 SEPARATION

    SciTech Connect

    Jerry Y.S. Lin

    2002-12-01

    This project is aimed at synthesis of a new inorganic dual-phase carbonate membrane for high temperature CO{sub 2} separation. Metal-carbonate dual-phase membranes were prepared by the direct infiltration method and the synthesis conditions were optimized. The dual-phase membranes are gas-tight with helium permeance about six orders of magnitude lower than that for the metal support. Efforts were made to test seals for permeation and separation experiments for dual-phase membrane at the intermediate temperature range (about 500 C) under oxidizing atmosphere. An effective new permeation cell with a metal seal was designed, fabricated and tested. The permeation setup provided leak-free sealing for the dual-phase membranes under the desired operation conditions. Though the reliable data showing high permeance for carbon dioxide with oxygen for the prepared metal-carbonate dual phase membrane has not been measured, the research efforts in improving membrane synthesis and setting up a new permeation cell with suitable seal have made it closer for one to demonstrate good dual-phase membranes for high temperature carbon dioxide separation. Research efforts were also directed towards preparation of a new ceramic-carbonate dual-phase membrane. Porous lanthanum cobaltite (LC) perovskite type oxide ceramic support with oxidation resistance better than the metal support and high electronic conductivity (1300-1500 S/cm in 400-600 C), was prepared and studied as an alternative support for the dual-phase carbonate membranes. The LC powder was found not reactive with the carbonate at 600 C. The porous LC disks have helium permeance and pore diameter smaller than the metal support but larger than the common {alpha}-alumina support. These results show promise to use the LC support for preparation of oxidation resistant dual-phase carbonate membranes.

  10. Ruthenium Behavior at Phase Separation of Borosilicate Glass-12259

    SciTech Connect

    Enokida, Youichi; Sawada, Kayo

    2012-07-01

    The Rokkasho reprocessing plant (RRP) located in Aomori, Japan, vitrifies high level waste (HLW) into a borosilicate glass. The HLW is generated from the reprocessing of spent fuel and contains ruthenium (Ru) and other platinum group metals (PGMs). Based on the recent consequences after a huge earthquake that occurred in Japan, a hypothetical blackout was postulated for the RRP to address additional safety analysis requirements. During a prolonged blackout, the borosilicate glass could phase separate due to cooling of the glass in the melter. The Ru present in the glass matrix could migrate into separate phases and impact the durability of the borosilicate glass. The durability of the glass is important for quality assurance and performance assessment of the vitrified HLW. A fundamental study was performed at an independent university to understand the impact of a prolonged blackout. Simulated HLW glasses were prepared for the RRP, and the Ru behavior in phase separated glasses was studied. The simulated HLW glasses contained nonradioactive elements and PGMs. The glass compositions were then altered to enhance the formation of the phase-separated glasses when subjected to thermal treatment at 700 deg. C for 24 hours. The synthesized simulated glasses contained 1.1 % Ru by weight as ruthenium dioxide (RuO{sub 2}). A portion of the RuO{sub 2} formed needle-shaped crystals in the glass specimens. After the thermal treatment, the glass specimen had separated into two phases. One of the two phases was a B{sub 2}O{sub 3} rich phase, and the other phase was a SiO{sub 2} rich phase. The majority of the chemical species in the B{sub 2}O{sub 3} rich phase was leached away with the Material Characterization Center-3 (MCC-3) protocol standardized by the Pacific Northwest National Laboratory using an aqueous low-concentrated nitric acid solution, but the leaching of the Ru fraction was very limited; less than 1% of the original Ru content. The Ru leaching was much less than

  11. Modeling Human Population Separation History Using Physically Phased Genomes

    PubMed Central

    Song, Shiya; Sliwerska, Elzbieta; Emery, Sarah; Kidd, Jeffrey M.

    2017-01-01

    Phased haplotype sequences are a key component in many population genetic analyses since variation in haplotypes reflects the action of recombination, selection, and changes in population size. In humans, haplotypes are typically estimated from unphased sequence or genotyping data using statistical models applied to large reference panels. To assess the importance of correct haplotype phase on population history inference, we performed fosmid pool sequencing and resolved phased haplotypes of five individuals from diverse African populations (including Yoruba, Esan, Gambia, Maasai, and Mende). We physically phased 98% of heterozygous SNPs into haplotype-resolved blocks, obtaining a block N50 of 1 Mbp. We combined these data with additional phased genomes from San, Mbuti, Gujarati, and Centre de’Etude du Polymorphism Humain European populations and analyzed population size and separation history using the pairwise sequentially Markovian coalescent and multiple sequentially Markovian coalescent models. We find that statistically phased haplotypes yield a more recent split-time estimation compared with experimentally phased haplotypes. To better interpret patterns of cross-population coalescence, we implemented an approximate Bayesian computation approach to estimate population split times and migration rates by fitting the distribution of coalescent times inferred between two haplotypes, one from each population, to a standard isolation-with-migration model. We inferred that the separation between hunter-gatherer populations and other populations happened ∼120–140 KYA, with gene flow continuing until 30–40 KYA; separation between west-African and out-of-African populations happened ∼70–80 KYA; while the separation between Maasai and out-of-African populations happened ∼50 KYA. PMID:28049708

  12. Phase separation in transparent liquid-liquid miscibility gap systems

    NASA Technical Reports Server (NTRS)

    Gelles, S. H.; Bhat, B. N.; Laub, R. J.

    1979-01-01

    A program to be carried out on transparent liquid-phase miscibility gap materials was developed for the purpose of acquiring additional insight into the separation process occurring in these systems. The transparency feature allows the reaction to be viewed directly through light scattering and holographic methods.

  13. Demixing kinetics of phase separated polymer solutions in microgravity

    NASA Technical Reports Server (NTRS)

    Brooks, D. E.; Bamberger, S. B.; Harris, J. M.; Vanalstine, J.; Snyder, R. S.

    1988-01-01

    Phase separated solutions of two neutral polymers in buffer provide a useful and versatile medium for the partition separation of biological cells. However, the efficiency of such separations is orders of magnitude lower than the thermodynamic limit. To test the hypothesis that this inefficiency is at least partially due to the convection and sedimentation that occur during the gravity driven demixing that follows introduction of cells to the systems, a series of experiments were begun aimed at performing cell partition in a low g environment. Demixing of isopycnic three polymer solvent systems was studied, experiments were performed on KC-135 aircraft and one shuttle middeck experiment was completed. Analysis of the results of these experiments and comparisons with the predictions of scaling relations for the dependence of phase domain size on time, derived for a number of possible demixing mechanisms, are presented.

  14. Diagnostic immunoassay by solid phase separation for digoxin

    SciTech Connect

    Grenier, F.C.; Pry, T.A.; Kolaczkowski, L.

    1988-11-29

    A method is described for conducting a diagnostic immunoassay for digoxin, comprising: (a) forming a reaction mixture of a test sample with a molar excess of labeled anti-digoxin antibodies whereby the labeled antibodies are capable of forming complex with digoxin present in the sample; (b) contacting the reaction mixture with a solid phase material having immobilized thereon a compound; (c) separating the solid phase material from the reaction mixture; and (d) determining the presence of digoxin in the test sample by measuring the amount of complex present in the liquid phase.

  15. Assemblages: Functional units formed by cellular phase separation

    PubMed Central

    Wright, Peter E.

    2014-01-01

    The partitioning of intracellular space beyond membrane-bound organelles can be achieved with collections of proteins that are multivalent or contain low-complexity, intrinsically disordered regions. These proteins can undergo a physical phase change to form functional granules or other entities within the cytoplasm or nucleoplasm that collectively we term “assemblage.” Intrinsically disordered proteins (IDPs) play an important role in forming a subset of cellular assemblages by promoting phase separation. Recent work points to an involvement of assemblages in disease states, indicating that intrinsic disorder and phase transitions should be considered in the development of therapeutics. PMID:25179628

  16. Binary mixtures of polyhedral nanoparticles: from phase separation to superstructures

    NASA Astrophysics Data System (ADS)

    Khadilkar, Mihir; Agarwal, Umang; Escobedo, Fernando

    2014-03-01

    Polyhedral nanoparticles have emerged as important model systems for both fundamental studies of entropic self-assembly as well as material design. The mixing of more than one shape provides a promising strategy towards achieving a greater variety of structures and properties. We explore this with the study of the phase behavior of binary mixtures of hard convex polyhedra having similar sizes but different shapes. Choosing representative particle shapes from those readily synthesizable, we find that the phase behavior of such mixtures is dependent on the interplay of mixing and packing entropy, which can give rise to miscible or phase-separated states. While expectedly many of the binary systems studied exhibit phase separation at high pressures due to the incompatible pure-component crystal structures, our study shows that the essential qualitative trends in miscibility and phase separation can be correlated to properties of the pure components, such as the relative values of the order-disorder transition pressure of each component. However, the relative size ratios and the presence of mesophases for the pure-component systems are also critical in aiding the formation of fully miscible blends of novel plastic crystalline superstructures.

  17. Analysis of Phase Separation in Czochralski Grown Single Crystal Ilmenite

    NASA Technical Reports Server (NTRS)

    Wilkins, R.; Powell, Kirk St. A.; Loregnard, Kieron R.; Lin, Sy-Chyi; Muthusami, Jayakumar; Zhou, Feng; Pandey, R. K.; Brown, Geoff; Hawley, M. E.

    1998-01-01

    Ilmenite (FeTiOs) is a wide bandgap semiconductor with an energy gap of 2.58 eV. Ilmenite has properties suited for radiation tolerant applications, as well as a variety of other electronic applications. Single crystal ilmenite has been grown from the melt using the Czochralski method. Growth conditions have a profound effect on the microstructure of the samples. Here we present data from a variety of analytical techniques which indicate that some grown crystals exhibit distinct phase separation during growth. This phase separation is apparent for both post-growth annealed and unannealed samples. Under optical microscopy, there appear two distinct areas forming a matrix with an array of dots on order of 5 pm diameter. While appearing bright in the optical micrograph, atomic force microscope (AFM) shows the dots to be shallow pits on the surface. Magnetic force microscope (MFM) shows the dots to be magnetic. Phase identification via electron microprobe analysis (EMPA) indicates two major phases in the unannealed samples and four in the annealed samples, where the dots appear to be almost pure iron. This is consistent with micrographs taken with a scanning probe microscope used in the magnetic force mode. Samples that do not exhibit the phase separation have little or no discernible magnetic structure detectable by the MFM.

  18. Phase separation dynamics during Myxococcus xanthus fruiting body formation

    NASA Astrophysics Data System (ADS)

    Liu, Guannan; Bahar, Fatmagul; Patch, Adam; Thutupalli, Shashi; Yllanes, David; Marchetti, M. Cristina; Welch, Roy; Shaevitz, Joshua

    Many living systems take advantage of collective behavior for group survival. We use the soil-dwelling bacterium Myxococcus xanthus as a model to study out-of-equilibrium phase separation during fruiting body formation. M. xanthus cells have the ability to glide on solid surfaces and reverse their direction periodically. When starved, M. xanthus cells aggregate together and form structures called fruiting bodies, inside of which cells sporulate to survive stressful conditions. We show that at high cell density the formation of fruiting bodies is a phase separation process. From experimental data that combines single-cell tracking, population-scale imaging, mutants, and drug applications, we construct the phase diagram of M. xanthus in the space of Péclet number and cell density. When wild type cells are starved, we find that they actively increase their Péclet number by modulating gliding speed and reversal frequency which induces a phase separation from a gas-like state to an aggregated fruiting body state.

  19. Phase separation in solutions with specific and nonspecific interactions

    SciTech Connect

    Jacobs, William M.; Frenkel, Daan; Oxtoby, David W.

    2014-05-28

    Protein solutions, which tend to be thermodynamically stable under physiological conditions, can demix into protein-enriched and protein-depleted phases when stressed. Using a lattice-gas model of proteins with both isotropic and specific, directional interactions, we calculate the critical conditions for phase separation for model proteins with up to four patches via Monte Carlo simulations and statistical associating fluid theory. Given a fixed specific interaction strength, the critical value of the isotropic energy, which accounts for dispersion forces and nonspecific interactions, measures the stability of the solution with respect to nonspecific interactions. Phase separation is suppressed by the formation of protein complexes, which effectively passivate the strongly associating sites on the monomers. Nevertheless, we find that protein models with three or more patches can form extended aggregates that phase separate despite the assembly of passivated complexes, even in the absence of nonspecific interactions. We present a unified view of the critical behavior of model fluids with anisotropic interactions, and we discuss the implications of these results for the thermodynamic stability of protein solutions.

  20. Re-entrant phase behavior for systems with competition between phase separation and self-assembly.

    PubMed

    Reinhardt, Aleks; Williamson, Alexander J; Doye, Jonathan P K; Carrete, Jesús; Varela, Luis M; Louis, Ard A

    2011-03-14

    In patchy particle systems where there is a competition between the self-assembly of finite clusters and liquid-vapor phase separation, re-entrant phase behavior can be observed, with the system passing from a monomeric vapor phase to a region of liquid-vapor phase coexistence and then to a vapor phase of clusters as the temperature is decreased at constant density. Here, we present a classical statistical mechanical approach to the determination of the complete phase diagram of such a system. We model the system as a van der Waals fluid, but one where the monomers can assemble into monodisperse clusters that have no attractive interactions with any of the other species. The resulting phase diagrams show a clear region of re-entrance. However, for the most physically reasonable parameter values of the model, this behavior is restricted to a certain range of density, with phase separation still persisting at high densities.

  1. Enantiomeric phase separation in a lattice gas model: Guggenheim approximation

    NASA Astrophysics Data System (ADS)

    Huckaby, Dale A.; Shinmi, Masato; Ausloos, Marcel; Clippe, Paulette

    1986-05-01

    We consider a lattice gas in which the two enantiomeric forms of a tetrahedral molecule, consisting of a central carbon atom bonded to four different groups A, B, G, and H, are adsorbed onto a triangular lattice, such that the carbon atom is above a lattice site, the three bonds to A, B, and G point toward neighboring lattice sites, and the bond to H points perpendicular to and away from the plane of the lattice. For a certain choice of intermolecular interactions, such as may exist between the zwitterion forms of an amino acid, the phase diagram was investigated using a Guggenheim approximation with two order parameters. Enantiomeric phase separation into two symmetric condensed phases occurs at low temperatures. These condensed phases become a single racemic condensed phase at a critical line, and they are in equilibrium with a racemic gas phase along a line of triple points. These two lines coincide at a critical endpoint. The racemic condensed and gas phases are in equilibrium along a two phase coexistence line which begins at the critical endpoint and ends at a critical point. No tricritical point was found in the model for the special choice of interactions studied.

  2. Growth and Morphology of Phase Separating Supercritical Fluids

    NASA Technical Reports Server (NTRS)

    Hegseth, John; Beysens, Daniel; Perrot, Francoise; Nikolayev, Vadim; Garrabos, Yves

    1996-01-01

    The scientific objective is to study the relation between the morphology and the growth kinetics of domains during phase separation. We know from previous experiments performed near the critical point of pure fluids and binary liquids that there are two simple growth laws at late times. The 'fast' growth appears when the volumes of the phases are nearly equal and the droplet pattern is interconnected. In this case the size of the droplets grows linearly in time. The 'slow' growth appears when the pattern of droplets embedded in the majority phase is disconnected. In this case the size of the droplets increases in proportion to time to the power 1/3. The volume fraction of the minority phase is a good candidate to determine this change of behavior. All previous attempts to vary the volume fraction in a single experimental cell have failed because of the extreme experimental difficulties.

  3. Phase separation of polymer thin films and some applications

    NASA Astrophysics Data System (ADS)

    Zhu, Shaoming

    Phase separation of polymer thin film is a common issue in polymer thin film application. The existence of surface and surfactant are understood to play an important role in thin film final topography. In chapter two, the configuration of polymer blend thin film phase separation on cobalt substrate with PMMA phase forming column structure, and PS phase encapsulating the PMMA phase was used as resist mask to transfer the topographical feature to cobalt thin film. Isolated near spherical single and multi domain magnetic islands were obtained. The island made using this method had a broad single domain range from below 1000 to 5000A. In chapter three, when the polymer blend thin film was in bilayer configuration and diblock copolymer was added on the top layer, we found the confinement can increase the mixing of two homopolymers in highly incompatible polymer blends. By affecting the formation of micelles, the copolymers are forced to the interface between the two homopolymer phases where they reduce the interfacial tension to zero and form a microemulsion. Our findings have two important implications: first, they elucidate the role entropy plays in determining the phase behaviour of confined polymer blends and second, they offer a simple pathway to create thin film coatings with precisely controlled properties and surfaces. In chapter four, the kinetics process of microemulsion formation in confinement configuration has been analyzed. The microemulsion formation proceeded at initial stage by capillary wave, then it followed the growth regime t1/3 and lnt, then followed a more slow growth regime (lnt).56 or (lnt).60 till finally reached equilibrium, when the structure was frozen. In chapter five, we study the evolution of the morphologies of polymer blend thin films on silicon, cobalt, and gold substrates. In asymmetrical system, the substrate surface energy determined the wetting degree of the substrate preferring phases. In chapter six, we present a novel method for

  4. Phase separation of metallic hydrogen-helium alloys

    NASA Technical Reports Server (NTRS)

    Straus, D. M.; Ashcroft, N. W.; Beck, H.

    1977-01-01

    Calculations are presented for the thermodynamic functions and phase-separation boundaries of solid metallic hydrogen-helium alloys at temperatures between zero and 19,000 K and at pressures between 15 and 90 Mbar. Expressions for the band-structure energy of a randomly disordered alloy (including third order in the electron-ion interaction) are derived and evaluated. Short- and long-range orders are included by the quasi-chemical method, and lattice dynamics in the virtual-crystal harmonic approximation. It is concluded that at temperatures below 4000 K, there is essentially complete phase separation of hydrogen-helium alloys and that a miscibility gap remains at the highest temperatures and pressures considered. The relevance of these results to models of the deep interior of Jupiter is briefly discussed.

  5. Phase separation of metallic hydrogen-helium alloys

    NASA Technical Reports Server (NTRS)

    Straus, D. M.; Ashcroft, N. W.; Beck, H.

    1976-01-01

    Calculations are presented for the thermodynamic functions and phase separation boundaries of solid metallic hydrogen helium alloys at temperatures between 0 K and 19,000 K and at pressures between 15 and 90 megabars. Expressions for the band structure energy of a randomly disordered alloy (including third order in the electron ion interaction) are derived and evaluated. Short and long range order are included by the quasi-chemical method, and lattice dynamics in the virtual crystal harmonic approximation. We conclude that at temperatures below 4,000 K there is complete phase separation of hydrogen helium alloys, and that a miscibility gap remains at the highest temperatures and pressures considered. The relevance of these results to models of the deep interior of Jupiter is briefly discussed.

  6. Kinetics of motility-induced phase separation and swim pressure

    NASA Astrophysics Data System (ADS)

    Patch, Adam; Yllanes, David; Marchetti, M. Cristina

    2017-01-01

    Active Brownian particles (ABPs) represent a minimal model of active matter consisting of self-propelled spheres with purely repulsive interactions and rotational noise. Here we examine the pressure of ABPs in two dimensions in both closed boxes and systems with periodic boundary conditions and show that its nonmonotonic behavior with density is a general property of ABPs and is not the result of finite-size effects. We correlate the time evolution of the mean pressure towards its steady-state value with the kinetics of motility-induced phase separation. For parameter values corresponding to phase-separated steady states, we identify two dynamical regimes. The pressure grows monotonically in time during the initial regime of rapid cluster formation, overshooting its steady-state value and then quickly relaxing to it, and remains constant during the subsequent slower period of cluster coalescence and coarsening. The overshoot is a distinctive feature of active systems.

  7. Fibril Formation and Phase Separation in Aqueous Cellulose Ethers

    NASA Astrophysics Data System (ADS)

    Maxwell, Amanda; Schmidt, Peter; McAllister, John; Lott, Joseph; Bates, Frank; Lodge, Timothy

    Aqueous solutions of many cellulose ethers are known to undergo thermoreversible gelation and phase separation upon heating to form turbid hydrogels, but the mechanism and resulting structures have not been well understood. Turbidity, light scattering and small-angle neutron scattering (SANS) are used to show that hydroxypropyl methylcellulose (HPMC) chains are dissolved in water below 50 °C and undergo phase separation at higher temperatures. At 70 °C, at sufficiently high concentrations in water, HPMC orders into fibrillar structures with a well-defined radius of 18 +/- 2 nm, as characterized by cryogenic transmission electron microscopy and SANS. The HPMC fibril structure is independent of concentration and heating rate. However, HPMC fibrils do not form a percolating network as readily as is seen in methylcellulose, resulting in a lower hot-gel modulus, as demonstrated by rheology.

  8. Correlated lateral phase separations in stacks of lipid membranes

    NASA Astrophysics Data System (ADS)

    Hoshino, Takuma; Komura, Shigeyuki; Andelman, David

    2015-12-01

    Motivated by the experimental study of Tayebi et al. [Nat. Mater. 11, 1074 (2012)] on phase separation of stacked multi-component lipid bilayers, we propose a model composed of stacked two-dimensional Ising spins. We study both its static and dynamical features using Monte Carlo simulations with Kawasaki spin exchange dynamics that conserves the order parameter. We show that at thermodynamical equilibrium, due to strong inter-layer correlations, the system forms a continuous columnar structure for any finite interaction across adjacent layers. Furthermore, the phase separation shows a faster dynamics as the inter-layer interaction is increased. This temporal behavior is mainly due to an effective deeper temperature quench because of the larger value of the critical temperature, Tc, for larger inter-layer interaction. When the temperature ratio, T/Tc, is kept fixed, the temporal growth exponent does not increase and even slightly decreases as a function of the increased inter-layer interaction.

  9. GPU accelerated numerical simulations of viscoelastic phase separation model.

    PubMed

    Yang, Keda; Su, Jiaye; Guo, Hongxia

    2012-07-05

    We introduce a complete implementation of viscoelastic model for numerical simulations of the phase separation kinetics in dynamic asymmetry systems such as polymer blends and polymer solutions on a graphics processing unit (GPU) by CUDA language and discuss algorithms and optimizations in details. From studies of a polymer solution, we show that the GPU-based implementation can predict correctly the accepted results and provide about 190 times speedup over a single central processing unit (CPU). Further accuracy analysis demonstrates that both the single and the double precision calculations on the GPU are sufficient to produce high-quality results in numerical simulations of viscoelastic model. Therefore, the GPU-based viscoelastic model is very promising for studying many phase separation processes of experimental and theoretical interests that often take place on the large length and time scales and are not easily addressed by a conventional implementation running on a single CPU.

  10. Correlated lateral phase separations in stacks of lipid membranes.

    PubMed

    Hoshino, Takuma; Komura, Shigeyuki; Andelman, David

    2015-12-28

    Motivated by the experimental study of Tayebi et al. [Nat. Mater. 11, 1074 (2012)] on phase separation of stacked multi-component lipid bilayers, we propose a model composed of stacked two-dimensional Ising spins. We study both its static and dynamical features using Monte Carlo simulations with Kawasaki spin exchange dynamics that conserves the order parameter. We show that at thermodynamical equilibrium, due to strong inter-layer correlations, the system forms a continuous columnar structure for any finite interaction across adjacent layers. Furthermore, the phase separation shows a faster dynamics as the inter-layer interaction is increased. This temporal behavior is mainly due to an effective deeper temperature quench because of the larger value of the critical temperature, Tc, for larger inter-layer interaction. When the temperature ratio, T/Tc, is kept fixed, the temporal growth exponent does not increase and even slightly decreases as a function of the increased inter-layer interaction.

  11. Tc anisotropy and phase separation in strained Vanadium Dioxide films

    NASA Astrophysics Data System (ADS)

    Liu, Mengkun; Wagner, Martin; Abreu, Elsa; Kittiwatanakul, Salinporn; McLeod, Alexander; Goldflam, Michael; Fei, Zhe; Dai, Siyuan; Fogler, Michael; Lu, Jiwei; Wolf, Stuart; Averitt, Richard; Basov, D. N.

    2013-03-01

    We report Infrared near field study on strain induced transition temperature (Tc) anisotropy in vanadium dioxide (VO2) films via direct visualization of a spontaneous structural and electronic phase separation. The films are epitaxially grown on [110]R or [100]R TiO2 substrates and exhibit large uniaxial strain. By mapping the film topography with AFM and electronic percolation with Infrared scattering scanning near-field optical microscopy, a temperature dependent electron-lattice correlation can be clearly observed. Our work sheds a new light onto the nature of the Tc anomaly in metal-insulator transition and leads to the possibility of controlling the material's properties through strain induced phase separation.

  12. Separation of granulocytes from whole blood by leukoadhesion, phase 1

    NASA Technical Reports Server (NTRS)

    1976-01-01

    Capillary glass tubes are investigated for the separation and retrieval of large quantities of viable granulocytes and monocytes from whole blood on a continuous basis from a single donor. This effort represented the feasibility demonstration of a three phase program for development of a capillary tube cell separation device. The activity included the analysis and parametric laboratory testing with subscale models required to design a prototype device. Capillary tubes 40 cm long with a nominal 0.030 cm internal diameter yielded the highest total process efficiency. Recovery efficiencies as high as 89% of the adhering cell population were obtained. Granulocyte phagocytosis of latex particles indicated approximately 90% viability. Monocytes recovered from the separation column retained their capability to stimulate human bone marrow colony growth, as demonstrated in an in vitro cell culture assay.

  13. Rationale for two phase polymer system microgravity separation experiments

    NASA Technical Reports Server (NTRS)

    Brooks, D. E.; Bamberger, S. B.; Harris, J. M.; Vanalstine, J.

    1984-01-01

    The two-phase systems that result when aqueous solutions of dextran and poly(ethylene glycol) are mixed at concentrations above a few percent are discussed. They provide useful media for the partition and isolation of macromolecules and cell subpopulations. By manipulating their composition, separations based on a variety of molecular and surface properties are achieved, including membrane hydrophobic properties, cell surface charge, and membrane antigenicity. Work on the mechanism of cell partition shows there is a randomizing, nonthermal energy present which reduces separation resolution. This stochastic energy is probably associated with hydrodynamic interactions present during separation. Because such factors should be markedly reduced in microgravity, a series of shuttle experiments to indicate approaches to increasing the resolution of the procedure are planned.

  14. Novel Resistive Switching Behavior in Phase Separated Manganites

    NASA Astrophysics Data System (ADS)

    Guo, Hangwen; Ward, T. Zac; Sun, Dali; Snijders, Paul C.; Gai, Zheng; Shen, Jian

    2011-03-01

    Electronic phase separation plays a key role in many novel phenomena in complex materials. Manganites are a prime example of this class of materials and have recently come under increase scrutiny for possible application in resistive random-access memory (RRAM) technology. Here, we will discuss our recent work on spatially confined La5/8-xPrxCa3/8MnO3. We have discovered that it is possible to drive single electronic domain formation/annihilation through electric field pulsing. By measuring the I-V curve, we find such resistive switching is different from normal RRAM mechanisms in manganites and is closely related to the nature of electronic phase separation. These findings open these systems to a new understanding of the nature of electronic phase separation and begin the development of manganites for future applications in RRAM devices. Research sponsored by the Division of Materials Sciences and Engineering, Office of Basic Energy Sciences, U.S. Department of Energy.

  15. Phase separated microstructure and dynamics of polyurethane elastomers under strain

    NASA Astrophysics Data System (ADS)

    Iacob, Ciprian; Padsalgikar, Ajay; Runt, James

    The molecular mobility of polyurethane elastomers is of the utmost importance in establishing physical properties for uses ranging from automotive tires and shoe soles to more sophisticated aerospace and biomedical applications. In many of these applications, chain dynamics as well as mechanical properties under external stresses/strains are critical for determining ultimate performance. In order to develop a more complete understanding of their mechanical response, we explored the effect of uniaxial strain on the phase separated microstructure and molecular dynamics of the elastomers. We utilize X-ray scattering to investigate soft segment and hard domain orientation, and broadband dielectric spectroscopy for interrogation of the dynamics. Uniaxial deformation is found to significantly perturb the phase-separated microstructure and chain orientation, and results in a considerable slowing down of the dynamics of the elastomers. Attenuated total reflectance Fourier transform infrared spectroscopy measurements of the polyurethanes under uniaxial deformation are also employed and the results are quantitatively correlated with mechanical tensile tests and the degree of phase separation from small-angle X-ray scattering measurements.

  16. Evaluation of phase separator number in hydrodesulfurization (HDS) unit

    NASA Astrophysics Data System (ADS)

    Jayanti, A. D.; Indarto, A.

    2016-11-01

    The removal process of acid gases such as H2S in natural gas processing industry is required in order to meet sales gas specification. Hydrodesulfurization (HDS)is one of the processes in the refinery that is dedicated to reduce sulphur.InHDS unit, phase separator plays important role to remove H2S from hydrocarbons, operated at a certain pressure and temperature. Optimization of the number of separator performed on the system is then evaluated to understand the performance and economics. From the evaluation, it shows that all systems were able to meet the specifications of H2S in the desired product. However, one separator system resulted the highest capital and operational costs. The process of H2S removal with two separator systems showed the best performance in terms of both energy efficiency with the lowest capital and operating cost. The two separator system is then recommended as a reference in the HDS unit to process the removal of H2S from natural gas.

  17. Uphill diffusion and phase separation in partially miscible multicomponent mixtures

    NASA Astrophysics Data System (ADS)

    He, Ping; Raghavan, Ashwin; Ghoniem, Ahmed

    2015-11-01

    The partially miscible multicomponent mixtures, which are frequently encountered in green chemistry processes, often exhibit complicated behaviors, and are critical to the production rate, energy efficiency, and pollution controls. Recent studies have been mainly focused on phase behaviors. However, the coupled phase equilibrium and transport process, which may be the answer to phase separations observed in experiments, is not well researched. Here, we present a numerical and theoretical study on coupled mixing of heavy oil and supercritical water, and the results of our state-of-art modeling agree with experimental measurements. We find that due to the non-ideal diffusion driving force, (1) strong uphill diffusion of heavy oil fractions occurs, (2) a new heavy oil phase is separated starting from the plait point, and heavy fractions become highly concentrated, and (3) water diffusion initially overshoots in oil, and is expelled lately. Finally, we conclude our analysis applicable to different molecules and conditions. The authors thank Saudi Aramco for supporting this work (contract number 6600023444).

  18. Thermodynamics of the motility-induced phase separation

    NASA Astrophysics Data System (ADS)

    Solon, Alexandre; Stenhammar, Joachim; Cates, Michael; Tailleur, Julien

    Self-propelled particles are known to accumulate in regions of space where their velocity is lowered. In addition, if their velocity diminishes when the local density increases (for example due to crowding effects), a positive feedback loop leads to the now well-established motility-induced phase separation (MIPS) between a dense immotile phase and a dilute motile phase. Understanding the phase equilibrium of MIPS is still a matter of debate. Although, depending on the models used to study the transition, a chemical potential or a pressure can be defined, these quantities do not play their usual thermodynamic role. In particular, the usual common tangent or equal-area constructions fail in these systems. Indeed, we will show that describing the phase equilibrium of MIPS necessitates generalized thermodynamics that include non-equilibrium contributions. This approach allows us to predict correctly the phase diagram of MIPS and to gain insight into the thermodynamics of active systems. It also sheds light on the (in)equivalence of statistical ensembles for these systems, paving the way for more efficient computational studies.

  19. Separation of peptides on superficially porous particle based macrocyclic glycopeptide liquid chromatography stationary phases: consideration of fast separations.

    PubMed

    Wimalasinghe, Rasangi M; Breitbach, Zachary S; Lee, Jauh T; Armstrong, Daniel W

    2017-03-01

    Macrocyclic glycopeptide based liquid chromatography stationary phases are known for their highly selective peptide separations. Fast and ultrafast (t R < 1 min) high-efficiency separations were achieved with superficially porous particle (SPP)-based stationary phases. Separations of pharmaceutically important classes of peptides such as enkephalins and bradykinins have been achieved in less than 5 min in isocratic elution modes. Selectivity for peptides structurally similar to one another was increased with use of teicoplanin-based stationary phases compared with commercial C18 stationary phases. Ultrafast isocratic separations of structurally related peptides were achieved with teicoplanin- and vancomycin-based short SPP columns. Acidic mobile phases produced better separations. Ammonium formate was the optimal mobile phase buffer additive. Use of an appropriate combination of a macrocyclic glycopeptide stationary phase and a mobile phase permits faster and more electrospray ionization mass spectrometry compatible isocratic separations than previous gradient approaches. The tryptic peptide separation characteristics of the teicoplanin stationary phase are demonstrated. Additionally, compared with commercial C18 stationary phases, teicoplanin showed tryptic peptide separations with different selectivities. Graphical Abstract Ultrafast separation of enkephalin peptide epimers.

  20. Quadruple-junction lattice coherency and phase separation in a binary-phase system

    PubMed Central

    Chung, Sung-Yoon; Choi, Si-Young; Kim, Jin-Gyu; Kim, Young-Min

    2015-01-01

    If each phase has an identical crystal structure and small misfit in the lattice parameters in a binary-phase crystalline system, coherent phase boundaries usually form during separation. Although there have been numerous studies on the effect of coherency elastic energy, no attempt has been made to demonstrate how the phase-separation behaviour varies when multiple interfaces meet at a junction. Here we show that a comprehensively different phase-separation morphology is induced, to release the high coherency strain confined to quadruple junctions. High-temperature in-situ transmission electron microscopy reveals that phase boundaries with a new crystallographic orientation emerge over twinned crystals to provide strain relaxation at quadruple junctions. The high coherency strain and the formation of different phase boundaries can be understood in terms of the force equilibrium between interface tensions at a junction point. Visualizing the quadruple points at atomic resolution, our observations emphasize the impact of multiple junctions on the morphology evolution during phase separation. PMID:26346223

  1. Influence of Side-Groups on Thermotropic Behavior of Polyorganophosphazenes

    DTIC Science & Technology

    1988-07-08

    Rather, these correlations depict how steric interactions associated with side group chemistry and dimensions influence the conformation of side groups ...OFFICE OF NAVAL RESEARCH Contract N00014-85-K-0358 Technical Report No. 8 INFLUENCE OF SIDE- GROUPS ON . j * ’A..,.. -Ti-ERMOTROPIC BEHAVIOR OF...5..i. * I L OFFICE OF NAVAL RESEARCH Contract N00014-85-K-0358 Technical Report No. 8 INFLUENCE OF SIDE- GROUPS ON THERMOTROPIC BEHAVIOR OF

  2. Macroscopic Phase Separation, Modulated Phases, and Microemulsions: A Unified Picture of Rafts

    PubMed Central

    Shlomovitz, Roie; Maibaum, Lutz; Schick, M.

    2014-01-01

    We simulate a simple phenomenological model describing phase behavior in a multicomponent membrane, a model capable of producing macroscopic phase separation, modulated phases, and microemulsions, all of which have been discussed in terms of raft phenomena. We show that one effect of thermal fluctuations on the mean-field phase diagram is that it permits a direct transition between either one of the coexisting liquid phases to a microemulsion. This implies that one system exhibiting phase separation can be related to a similar system exhibiting the heterogeneities characteristic of a microemulsion. The two systems could differ in their average membrane composition or in the relative compositions of their exoplasmic and cytoplasmic leaves. The model provides a unified description of these raft-associated phenomena. PMID:24806930

  3. The phase reversal phenomenon at flow separation and reattachment

    NASA Technical Reports Server (NTRS)

    Stack, J. Pete; Mangalam, S. M.; Kalburgi, V.

    1988-01-01

    Tests were conducted on two different airfoils, one of them in a low-turbulence tunnel, to detect laminar separation and turbulent reattachment locations. A 'nonintrusive' multielement sensor consisting of a large number of closely spaced individual nickel films was vacuum deposited on a thin substrate and bonded to the airfoil model surface. Each sensor element was a part of an independent constant temperature anemometer system. Time history as well as spectral analysis of signals from surface film gauges were used to determine the surface shear flow characteristics. A major breakthrough was achieved with the discovery of phase reversal in low-frequency dynamic shear stress signals across regions of flow separation and reattachment.

  4. Competing phases, phase separation, and coexistence in the extended one-dimensional bosonic Hubbard model

    SciTech Connect

    Batrouni, G. G.; Rousseau, V. G.; Scalettar, R. T.; Grémaud, B.

    2014-11-17

    Here, we study the phase diagram of the one-dimensional bosonic Hubbard model with contact (U) and near neighbor (V ) interactions focusing on the gapped Haldane insulating (HI) phase which is characterized by an exotic nonlocal order parameter. The parameter regime (U, V and μ) where this phase exists and how it competes with other phases such as the supersolid (SS) phase, is incompletely understood. We use the Stochastic Green Function quantum Monte Carlo algorithm as well as the density matrix renormalization group to map out the phase diagram. The HI exists only at = 1, the SS phase exists for a very wide range of parameters (including commensurate fillings) and displays power law decay in the one body Green function were our main conclusions. Additionally, we show that at fixed integer density, the system exhibits phase separation in the (U, V ) plane.

  5. Competing phases, phase separation, and coexistence in the extended one-dimensional bosonic Hubbard model

    DOE PAGES

    Batrouni, G. G.; Rousseau, V. G.; Scalettar, R. T.; ...

    2014-11-17

    Here, we study the phase diagram of the one-dimensional bosonic Hubbard model with contact (U) and near neighbor (V ) interactions focusing on the gapped Haldane insulating (HI) phase which is characterized by an exotic nonlocal order parameter. The parameter regime (U, V and μ) where this phase exists and how it competes with other phases such as the supersolid (SS) phase, is incompletely understood. We use the Stochastic Green Function quantum Monte Carlo algorithm as well as the density matrix renormalization group to map out the phase diagram. The HI exists only at = 1, the SS phase existsmore » for a very wide range of parameters (including commensurate fillings) and displays power law decay in the one body Green function were our main conclusions. Additionally, we show that at fixed integer density, the system exhibits phase separation in the (U, V ) plane.« less

  6. Self-assembly of amorphous biophotonic nanostructures by phase separation

    SciTech Connect

    Dufresne, Eric R.; Noh, Heeso; Saranathan, Vinodkumar; Mochrie, Simon G.J.; Cao, Hui; Prum, Richard O.

    2009-04-23

    Some of the most vivid colors in the animal kingdom are created not by pigments, but by wavelength-selective scattering of light from nanostructures. Here we investigate quasi-ordered nanostructures of avian feather barbs which produce vivid non-iridescent colors. These {beta}-keratin and air nanostructures are found in two basic morphologies: tortuous channels and amorphous packings of spheres. Each class of nanostructure is isotropic and has a pronounced characteristic length scale of variation in composition. These local structural correlations lead to strong backscattering over a narrow range of optical frequencies and little variation with angle of incidence. Such optical properties play important roles in social and sexual communication. To be effective, birds need to precisely control the development of these nanoscale structures, yet little is known about how they grow. We hypothesize that multiple lineages of birds have convergently evolved to exploit phase separation and kinetic arrest to self-assemble spongy color-producing nanostructures in feather barbs. Observed avian nanostructures are strikingly similar to those self-assembled during the phase separation of fluid mixtures; the channel and sphere morphologies are characteristic of phase separation by spinodal decomposition and nucleation and growth, respectively. These unstable structures are locked-in by the kinetic arrest of the {beta}-keratin matrix, likely through the entanglement or cross-linking of supermolecular {beta}-keratin fibers. Using the power of self-assembly, birds can robustly realize a diverse range of nanoscopic morphologies with relatively small physical and chemical changes during feather development.

  7. Vapors-liquid phase separator. [infrared telescope heat sink

    NASA Technical Reports Server (NTRS)

    Frederking, T. H. K.; Brown, G. S.; Chuang, C.; Kamioka, Y.; Kim, Y. I.; Lee, J. M.; Yuan, S. W. K.

    1980-01-01

    The use of porous plugs, mostly with in the form of passive devices with constant area were considered as vapor-liquid phase separators for helium 2 storage vessels under reduced gravity. The incorporation of components with variable cross sectional area as a method of flow rate modification was also investigated. A particular device which uses a shutter-type system for area variation was designed and constructed. This system successfully permitted flor rate changes of up to plus or minus 60% from its mean value.

  8. Nanopatterns by phase separation of patterned mixed polymer monolayers

    DOEpatents

    Huber, Dale L; Frischknecht, Amalie

    2014-02-18

    Micron-size and sub-micron-size patterns on a substrate can direct the self-assembly of surface-bonded mixed polymer brushes to create nanoscale patterns in the phase-separated mixed polymer brush. The larger scale features, or patterns, can be defined by a variety of lithographic techniques, as well as other physical and chemical processes including but not limited to etching, grinding, and polishing. The polymer brushes preferably comprise vinyl polymers, such as polystyrene and poly(methyl methacrylate).

  9. Phase/Shape Transitions and the Two Neutron Separation Energies

    SciTech Connect

    Zamfir, N. V.; Anghel, Sabina; Cata-Danil, G.

    2008-11-11

    We investigated the evolution of experimental two-neutron separation energies (S{sub 2n}) along the isotopic chains for the even-even nuclei. In order to enhance the sensitivity of our search, differential variation of the S{sub 2n} has been investigated. The emphasis is on finding nonmonotonic behaviors which can be correlated with phase/shape transition. Correlations of the ground state S{sub 2n} values with the excited states energies R{sub 4/2} ratio are also discussed.

  10. Anomalous Phase Separation Kinetics Observed in a Micelle Solution

    NASA Astrophysics Data System (ADS)

    Wilcoxon, Jess P.; Martin, James E.; Odinek, Judy

    1995-08-01

    We report a real-time, two-dimensional light scattering study of the evolution of structure in a two-component nonionic micelle system undergoing phase separation. We find that the structure of the domains is qualitatively similar to that observed in binary fluid systems, with some anomalies observed. However, compared to the Lifshitz-Slyozov prediction for simple binary fluids, the domain growth is unexpectedly slow. In fact, the growth kinetics can be empirically described as a stretched exponential approach to a pinned domain size. This anomalous behavior may be due to the ability of the spherical micelles to reorganize into more complex structures.

  11. Polymer-induced phase separation in suspensions of bacteria

    NASA Astrophysics Data System (ADS)

    Schwarz-Linek, J.; Dorken, G.; Winkler, A.; Wilson, L. G.; Pham, N. T.; French, C. E.; Schilling, T.; Poon, W. C. K.

    2010-03-01

    We study phase separation in suspensions of two unrelated species of rod-like bacteria, Escherichia coli and Sinorhizobium meliloti, induced by the addition of two different anionic polyelectrolytes, sodium polystyrene sulfonate or succinoglycan, the former being synthetic and the latter of natural origin. Comparison with the known behaviour of synthetic colloid-polymer mixtures and with simulations show that "depletion" (or, equivalently, "macromolecular crowding") is the dominant mechanism: exclusion of the non-adsorbing polymer from the region between two neighbouring bacteria creates an unbalanced osmotic force pushing them together. The implications of our results for understanding phenomena such as biofilm formation are discussed.

  12. Characterization of Phase Separation Propensity for Amorphous Spray Dried Dispersions.

    PubMed

    McNamara, Daniel; Yin, Shawn; Pan, Duohai; Crull, George; Timmins, Peter; Vig, Balvinder

    2017-02-06

    A generalized screening approach, applying isothermal calorimetry at 37 °C 100% RH, to formulations of spray dried dispersions (SDDs) for two active pharmaceutical ingredients (APIs) (BMS-903452 and BMS-986034) is demonstrated. APIs 452 and 034, with similar chemotypes, were synthesized and promoted during development for oral dosing. Both APIs were formulated as SDDs for animal exposure studies using the polymer hydroxypropylmethlycellulose acetyl succinate M grade (HPMCAS-M). 452 formulated at 30% (wt/wt %) was an extremely robust SDD that was able to withstand 40 °C 75% RH open storage conditions for 6 months with no physical evidence of crystallization or loss of dissolution performance. Though 034 was a chemical analogue with similar physical chemical properties to 452, a physically stable SDD of 034 could not be formulated in HPMCAS-M at any of the drug loads attempted. This study was used to develop experience with specific physical characterization laboratory techniques to evaluate the physical stability of SDDs and to characterize the propensity of SDDs to phase separate and possibly crystallize. The screening strategy adopted was to stress the formulated SDDs with a temperature humidity screen, within the calorimeter, and to apply orthogonal analytical techniques to gain a more informed understanding of why these SDDs formulated with HPMCAS-M demonstrated such different physical stability. Isothermal calorimetry (thermal activity monitor, TAM) was employed as a primary stress screen wherein the SDD formulations were monitored for 3 days at 37 °C 100% RH for signs of phase separation and possible crystallization of API. Powder X-ray diffraction (pXRD), modulated differential scanning calorimetry (mDSC), Fourier transform infrared spectroscopy (FTIR), and solid state nuclear magnetic resonance (ssNMR) were all used to examine formulated SDDs and neat amorphous drug. 452 SDDs formulated at 30% (wt/wt %) or less did not show phase separation behavior upon

  13. Children in divorce: intervention in the phase of separation.

    PubMed

    Derdeyn, A P

    1977-07-01

    Divorce of their parents can create difficulties for the development of young children. The ability of children to integrate the various losses involved in the breaking up of a family is impeded by limitations of their cognitive understanding of events taking place during the separation phase. Because their thinking process is as yet immature, children often feel responsible for the divorce, and they otherwise distort the meaning of the events about them. The pediatrician can often guide and encourage parents to facilitate their children's understanding and acceptance of the changes in their lives.

  14. Vortex motion phase separator for zero gravity liquid transfer

    NASA Technical Reports Server (NTRS)

    Howard, Frank S. (Inventor); Fraser, Wilson M., Jr. (Inventor)

    1989-01-01

    A vortex motion phase separator is disclosed for transferring a liquid in a zero gravity environment while at the same time separating the liquid from vapors found within either the sender or the receiving tanks. The separator comprises a rigid sender tank having a circular cross-section and rigid receiver tank having a circular cross-section. A plurality of ducts connects the sender tank and the receiver tank. Disposed within the ducts connecting the receiver tank and the sender tank is a pump and a plurality of valves. The pump is powered by an electric motor and is adapted to draw either the liquid or a mixture of the liquid and the vapor from the sender tank. Initially, the mixture drawn from the sender tank is directed through a portion of the ductwork and back into the sender tank at a tangent to the inside surface of the sender tank, thereby creating a swirling vortex of the mixture within the sender tank. As the pumping action increases, the speed of the swirling action within the sender tank increases creating an increase in the centrifugal force operating on the mixture. The effect of the centrifugal force is to cause the heavier liquid to migrate to the inside surface of the sender tank and to separate from the vapor. When this separation reaches a predetermined degree, control means is activated to direct the liquid conveyed by the pump directly into the receiver tank. At the same time, the vapor within the receiver tank is directed from the receiver tank back into the sender tank. This flow continues until substantially all of the liquid is transferred from the sender tank to the receiver tank.

  15. Digital holographic microscopy of phase separation in multicomponent lipid membranes

    NASA Astrophysics Data System (ADS)

    Farzam Rad, Vahideh; Moradi, Ali-Reza; Darudi, Ahmad; Tayebi, Lobat

    2016-12-01

    Lateral in-homogeneities in lipid compositions cause microdomains formation and change in the physical properties of biological membranes. With the presence of cholesterol and mixed species of lipids, phospholipid membranes segregate into lateral domains of liquid-ordered and liquid-disordered phases. Coupling of two-dimensional intralayer phase separations and interlayer liquid-crystalline ordering in multicomponent membranes has been previously demonstrated. By the use of digital holographic microscopy (DHMicroscopy), we quantitatively analyzed the volumetric dynamical behavior of such membranes. The specimens are lipid mixtures composed of sphingomyelin, cholesterol, and unsaturated phospholipid, 1,2-dioleoyl-sn-glycero-3-phosphocholine. DHMicroscopy in a transmission mode is an effective tool for quantitative visualization of phase objects. By deriving the associated phase changes, three-dimensional information on the morphology variation of lipid stacks at arbitrary time scales is obtained. Moreover, the thickness distribution of the object at demanded axial planes can be obtained by numerical focusing. Our results show that the volume evolution of lipid domains follows approximately the same universal growth law of previously reported area evolution. However, the thickness of the domains does not alter significantly by time; therefore, the volume evolution is mostly attributed to the changes in area dynamics. These results might be useful in the field of membrane-based functional materials.

  16. Modeling reaction fronts of separated condensed phase reactants

    NASA Astrophysics Data System (ADS)

    Koundinyan, Sushilkumar; Stewart, D. Scott; Matalon, Moshe

    2017-01-01

    We present a Gibbs free energy approach to modeling reaction fronts in condensed phase reactive materials. The current interest is in chemical reactions of condensed phase reactants that are initially separated. In energetic materials such reactions are observed to occur extremely fast and at relatively sharp fronts. The condensed phase combustion process differs in several aspects from classical gaseous combustion due to the disparity between the characteristic thermal conductivity length and the mass diffusion lengths and a volume, temperature, stress, mass fraction equation of state that principally depends only on the component reference volumes and the current mixture composition. To retain a simple planar configuration, we consider the two reactants, in solid phase, are in motion towards each other characterized by counter-flow geometry. We apply the model to a simplified Titanium-Boron system and present the analysis of reaction zone length for various strain rates. The numerical results are validated with asymptotic approximations at the Burke-Schumann (complete combustion) limit.

  17. Phase Separation in Lean Grade Duplex Stainless Steel 2101

    SciTech Connect

    Garfinkel, D.; Poplawsky, Jonathan D.; Guo, Wei; Young, Jr., George A.; Tucker, Julie

    2015-08-19

    The use of duplex stainless steels (DSS) in nuclear power generation systems is limited by thermal instability that leads to embrittlement in the temperature range of 204°C - 538°C. New lean grade alloys, such as 2101, offer the potential to mitigate these effects. Thermal embrittlement was quantified through impact toughness and hardness testing on samples of alloy 2101 after aging at 427°C for various durations (1-10,000 hours). Additionally, atom probe tomography (APT) was utilized in order to observe the kinetics of α-α’ separation and G-phase formation. Mechanical testing and APT data for two other DSS alloys, 2003 and 2205 were used as a reference to 2101. The results show that alloy 2101 exhibits superior performance compared to the standard grade DSS alloy, 2205, but inferior to the lean grade alloy, 2003, in mechanical testing. APT data demonstrates that the degree of α-α’ separation found in alloy 2101 closely resembles that of 2205, and greatly exceeds 2003. Additionally, contrary to what was observed in 2003, 2101 demonstrated G-phase like precipitates after long aging times, though precipitates were not as abundant as was observed in 2205.

  18. Dynamic phase separation: from coarsening to turbulence via structure formation.

    PubMed

    Golovin, A A; Pismen, L M

    2004-09-01

    We investigate some new two-dimensional evolution models belonging to the class of convective Cahn-Hilliard models: (i) a local model with a scalar order parameter, (ii) a nonlocal model with a scalar order parameter, and (iii) a model with a vector order parameter. These models are applicable to phase-separating system where concentration gradients cause hydrodynamic motion due to buoyancy or Marangoni effect. The numerical study of the models shows transition from coarsening, typical of Cahn-Hilliard systems, to spatiotemporally irregular behavior (turbulence), typical of the Kuramoto-Sivashinsky equation, which is obtained in the limit of very strong driving. The transition occurs not in a straightforward way, but through the formation of spatial patterns that emerge for intermediate values of the driving intensity. As in driven one-dimensional models studied before, the mere presence of the driving force, however small, breaks the symmetry between the two separating phases, as well as increases the coarsening rate. With increasing driving, coarsening stops. The dynamics is generally irregular at strong driving, but exhibits specific structural features.

  19. The mechanical properties of phase separated protein droplets

    NASA Astrophysics Data System (ADS)

    Jawerth, Louise; Ijavi, Mahdiye; Patel, Avinash; Saha, Shambaditya; Jülicher, Frank; Hyman, Anthony

    In vivo, numerous proteins associate into liquid compartments by de-mixing from the surrounding solution, similar to oil molecules in water. Many of these proteins and their corresponding liquid compartments play a crucial role in important biological processes, for instance germ line specification in C. elegans or in neurodegenerative diseases such as Amyotrophic lateral sclerosis (ALS). However, despite their importance, very little is known about the physical properties of the resulting droplets as well as the physical mechanisms that control their phase separation from solution. To gain a deeper understanding of these aspects, we study a few such proteins in vitro. When these proteins are purified and added to a physiological buffer, they phase separate into droplets ranging in size from a few to tens of microns with liquid-like behavior similar to their physiological counterparts. By attaching small beads to the surface of the droplets, we can deform the droplets by manipulating the beads directly using optical tweezers. By measuring the force required to deform the droplets we determine their surface tension, elasticity and viscosity as well as the frequency response of these properties. We also measure these properties using passive micro-rheology.

  20. Correlated lateral phase separations in stacks of lipid membranes

    SciTech Connect

    Hoshino, Takuma; Komura, Shigeyuki; Andelman, David

    2015-12-28

    Motivated by the experimental study of Tayebi et al. [Nat. Mater. 11, 1074 (2012)] on phase separation of stacked multi-component lipid bilayers, we propose a model composed of stacked two-dimensional Ising spins. We study both its static and dynamical features using Monte Carlo simulations with Kawasaki spin exchange dynamics that conserves the order parameter. We show that at thermodynamical equilibrium, due to strong inter-layer correlations, the system forms a continuous columnar structure for any finite interaction across adjacent layers. Furthermore, the phase separation shows a faster dynamics as the inter-layer interaction is increased. This temporal behavior is mainly due to an effective deeper temperature quench because of the larger value of the critical temperature, T{sub c}, for larger inter-layer interaction. When the temperature ratio, T/T{sub c}, is kept fixed, the temporal growth exponent does not increase and even slightly decreases as a function of the increased inter-layer interaction.

  1. Phase Separation in Lean Grade Duplex Stainless Steel 2101

    DOE PAGES

    Garfinkel, D.; Poplawsky, Jonathan D.; Guo, Wei; ...

    2015-08-19

    The use of duplex stainless steels (DSS) in nuclear power generation systems is limited by thermal instability that leads to embrittlement in the temperature range of 204°C - 538°C. New lean grade alloys, such as 2101, offer the potential to mitigate these effects. Thermal embrittlement was quantified through impact toughness and hardness testing on samples of alloy 2101 after aging at 427°C for various durations (1-10,000 hours). Additionally, atom probe tomography (APT) was utilized in order to observe the kinetics of α-α’ separation and G-phase formation. Mechanical testing and APT data for two other DSS alloys, 2003 and 2205 weremore » used as a reference to 2101. The results show that alloy 2101 exhibits superior performance compared to the standard grade DSS alloy, 2205, but inferior to the lean grade alloy, 2003, in mechanical testing. APT data demonstrates that the degree of α-α’ separation found in alloy 2101 closely resembles that of 2205, and greatly exceeds 2003. Additionally, contrary to what was observed in 2003, 2101 demonstrated G-phase like precipitates after long aging times, though precipitates were not as abundant as was observed in 2205.« less

  2. Liquid-Liquid Phase Separation of Oil Bodies from Seeds.

    PubMed

    Nykiforuk, Cory L

    2016-01-01

    Fundamentally, oil bodies are discrete storage organelles found in oilseeds, comprising a hydrophobic triacylglycerol core surrounded by a half-unit phospholipid membrane and an outer shell of specialized proteins known as oleosins. Oil bodies possess a number of attributes that were exploited by SemBioSys Genetics to isolate highly enriched fractions of oil bodies through liquid-liquid phase separation for a number of commercial applications. The current chapter provides a general guide for the isolation of oil bodies from Arabidopsis and/or safflower seed, from which protocols can be refined for different oilseed sources. For SemBioSys Genetic's recombinant technology, therapeutic proteins were covalently attached to oleosins or fused in-frame with ligands which bound oil bodies, facilitating their recovery to high levels of purity during "upstream processing" of transformed seed. Core to this technology was oil body isolation consisting of simple manipulation including homogenization of seeds to free the oil bodies, followed by the removal of insoluble fractions, and phase separation to recover the oil bodies. During oil body enrichment (an increase in oil body content concomitant with removal of impurities), a number of options and tips are provided to aid researchers in the manipulation and monitoring of these robust organelles.

  3. Modeling reaction fronts of separated condensed phase reactants

    NASA Astrophysics Data System (ADS)

    Koundinyan, Sushilkumar; Matalon, Moshe; Stewart, D. Scott; Bdzil, John

    2015-06-01

    We present a Gibbs free energy approach to modeling reaction fronts in condensed phase reactive materials. The current interest is in chemical reactions of condensed phase reactants that are initially separated. In energetic materials such reactions are observed to occur extremely fast and at relatively sharp fronts. The solid-to-solid combustion process differs in several aspects from classical gaseous combustion due to the disparity between the characteristic thermal conductivity length and the mass diffusion lengths and a volume, temperature, stress, mass fraction equation of state that principally depends only on the component reference volumes and the current mixture composition. To retain a simple planar configuration, we consider the two reactants, in solid phase, are in motion towards each other characterized by counter-flow geometry. We apply the model to a simplified Titanium-Boron system and present the analysis of reaction zone length for various strain rates. The numerical results are validated with asymptotic approximations at the Burke-Schumann limit. Supported by HDTRA1-10-1-0020 (DTRA), AF Sub MO C00039417-1 (AFOSR/TRE).

  4. Dual Phase Membrane for High Temperature CO2 Separation

    SciTech Connect

    Jerry Lin

    2007-06-30

    This project aimed at synthesis of a new inorganic dual-phase carbonate membrane for high temperature CO{sub 2} separation. Metal-carbonate dual-phase membranes were prepared by the direct infiltration method and the synthesis conditions were optimized. Permeation tests for CO{sub 2} and N{sub 2} from 450-750 C showed very low permeances of those two gases through the dual-phase membrane, which was expected due to the lack of ionization of those two particular gases. Permeance of the CO{sub 2} and O{sub 2} mixture was much higher, indicating that the gases do form an ionic species, CO{sub 3}{sup 2-}, enhancing transport through the membrane. However, at temperatures in excess of 650 C, the permeance of CO{sub 3}{sup 2-} decreased rapidly, while predictions showed that permeance should have continued to increase with temperature. XRD data obtained from used membrane indicated that lithium iron oxides formed on the support surface. This lithium iron oxide layer has a very low conductivity, which drastically reduces the flow of electrons to the CO{sub 2}/O{sub 2} gas mixture; thus limiting the formation of the ionic species required for transport through the membrane. These results indicated that the use of stainless steel supports in a high temperature oxidative environment can lead to decreased performance of the membranes. This revelation created the need for an oxidation resistant support, which could be gained by the use of a ceramic-type membrane. Work was extended to synthesize a new inorganic dual-phase carbonate membrane for high temperature CO{sub 2} separation. Helium permeance of the support before and after infiltration of molten carbonate are on the order of 10{sup -6} and 10{sup -10} moles/m{sup 2} {center_dot} Pa {center_dot} s respectively, indicating that the molten carbonate is able to sufficiently infiltrate the membrane. It was found that La{sub 0.6}Sr{sub 0.4}Co{sub 0.8}Fe{sub 0.2}O{sub 3-{delta}} (LSCF) was a suitable candidate for the support

  5. Tobacco protein separation by aqueous two-phase extraction.

    PubMed

    Balasubramaniam, Deepa; Wilkinson, Carol; Van Cott, Kevin; Zhang, Chenming

    2003-03-07

    Tobacco has long been considered as a host to produce large quantity of high-valued recombinant proteins. However, dealing with large quantities of biomass is a challenge for downstream processing. Aqueous two-phase extraction (ATPE) has been widely used in purifying proteins from various sources. It is a protein-friendly process and can be scaled up easily. In this paper, ATPE was studied for its applicability to recombinant protein purification from tobacco with egg white lysozyme as the model protein. Separate experiments with poly(ethylene glycol) (PEG)-salt-tobacco extract and PEG-salt-lysozyme were carried out to determine the partition behavior of tobacco protein and lysozyme, respectively. Two-level fractional factorial designs were used to study the effects of factors such as, PEG molecular mass, PEG concentration, the concentration of phase forming salt, sodium chloride concentration and pH, on protein partitioning. The results showed that, among the studied systems, PEG-sodium sulfate system was most suitable for lysozyme purification. Detailed experiments were conducted by spiking lysozyme into the tobacco extract. The conditions with highest selectivity of lysozyme over native tobacco protein were determined using a response surface design. The purification factor was further improved by decreasing the phase ratio along the tie line corresponding to the phase compositions with the highest selectivity. Under selected conditions the lysozyme yield was predicted to be 87% with a purification factor of 4 and concentration factor of 14. From this study, ATPE was shown to be suitable for initial protein recovery and partial purification from transgenic tobacco.

  6. Model system studies with a phase separated membrane bioreactor

    NASA Technical Reports Server (NTRS)

    Petersen, G. R.; Seshan, P. K.; Dunlop, Eric H.

    1989-01-01

    The operation and evaluation of a bioreactor designed for high intensity oxygen transfer in a microgravity environment is described. The reactor itself consists of a zero headspace liquid phase separated from the air supply by a long length of silicone rubber tubing through which the oxygen diffuses in and the carbon dioxide diffuses out. Mass transfer studies show that the oxygen is film diffusion controlled both externally and internally to the tubing and not by diffusion across the tube walls. Methods of upgrading the design to eliminate these resistances are proposed. Cell growth was obtained in the fermenter using Saccharomyces cerevisiae showing that this concept is capable of sustaining cell growth in the terrestial simulation.

  7. Phase separated membrane bioreactor - Results from model system studies

    NASA Technical Reports Server (NTRS)

    Petersen, G. R.; Seshan, P. K.; Dunlop, E. H.

    1989-01-01

    The operation and evaluation of a bioreactor designed for high intensity oxygen transfer in a microgravity environment is described. The reactor itself consists of a zero headspace liquid phase separated from the air supply by a long length of silicone rubber tubing through which the oxygen diffuses in and the carbon dioxide diffuses out. Mass transfer studies show that the oxygen is film diffusion controlled both externally and internally to the tubing and not by diffusion across the tube walls. Methods of upgrading the design to eliminate these resistances are proposed. Cell growth was obtained in the fermenter using Saccharomyces cerevisiae showing that this concept is capable of sustaining cell growth in the terrestrial simulation.

  8. The evolutionary significance of phase-separated microsystems

    NASA Technical Reports Server (NTRS)

    Fox, S. W.

    1976-01-01

    The source, preparation, and properties of phase-separated systems such as lipid layers, coacervate droplets, sulphobes, and proteinoid microspheres are reviewed. These microsystems are of interest as partial models for the cell and as partial or total models for the protocell. Conceptual benefits from the study of such models include clues to experiments on origins, insights into principles of action, and, in some instances, presumable models of the origin of the protocell. The benefits to evolution of organized chemical units are many, and can in part be analyzed. Ease of formation suggests that such units would have arisen early in primordial organic evolution. Integration of these various concepts and the results of consequent experiments have contributed to the developing theory of the origins of primordial and contemporary life.

  9. Chronotaxic systems with separable amplitude and phase dynamics

    NASA Astrophysics Data System (ADS)

    Suprunenko, Yevhen F.; Clemson, Philip T.; Stefanovska, Aneta

    2014-01-01

    Until recently, deterministic nonautonomous oscillatory systems with stable amplitudes and time-varying frequencies were not recognized as such and have often been mistreated as stochastic. These systems, named chronotaxic, were introduced in Phys. Rev. Lett. 111, 024101 (2013), 10.1103/PhysRevLett.111.024101. In contrast to conventional limit cycle models of self-sustained oscillators, these systems posses a time-dependent point attractor or steady state. This allows oscillations with time-varying frequencies to resist perturbations, a phenomenon which is ubiquitous in living systems. In this work a detailed theory of chronotaxic systems is presented, specifically in the case of separable amplitude and phase dynamics. The theory is extended by the introduction of chronotaxic amplitude dynamics. The wide applicability of chronotaxic systems to a range of fields from biological and condensed matter systems to robotics and control theory is discussed.

  10. Phase separated membrane bioreactor: results from model system studies.

    PubMed

    Petersen, G R; Seshan, P K; Dunlop, E H

    1989-01-01

    The operation and evaluation of a bioreactor designed for high intensity oxygen transfer in a microgravity environment is described. The reactor itself consists of a zero headspace liquid phase separated from the air supply by a long length of silicone rubber tubing through which the oxygen diffuses in and the carbon dioxide diffuses out. Mass transfer studies show that the oxygen is film diffusion controlled both externally and internally to the tubing and not by diffusion across the tube walls. Methods of upgrading the design to eliminate these resistances are proposed. Cell growth was obtained in the fermenter using Saccharomyces cerevisiae showing that this concept is capable of sustaining cell growth in the terrestrial [correction of terrestial] simulation.

  11. Electronic phase separation transition as the origin of the superconductivity and pseudogap phase of cuprates

    NASA Astrophysics Data System (ADS)

    de Mello, E. V. L.; Kasal, R. B.; Passos, C. A. C.

    2009-06-01

    To deal with the physics of cuprate superconductivity we propose an electronic phase separation transition that segregates the holes into high and low density domains. The calculated grain boundary potential favors the development of intragrain superconducting amplitudes. The zero resistivity transition arises only when the intergrain Josephson coupling EJ is of the order of the thermal energy and phase locking takes place among the superconducting grains. We show that this approach explains the pseudogap and superconducting phases and it also reproduces some recent scanning tunneling microscopy data.

  12. Electronic phase separation transition as the origin of the superconductivity and pseudogap phase of cuprates.

    PubMed

    de Mello, E V L; Kasal, R B; Passos, C A C

    2009-06-10

    To deal with the physics of cuprate superconductivity we propose an electronic phase separation transition that segregates the holes into high and low density domains. The calculated grain boundary potential favors the development of intragrain superconducting amplitudes. The zero resistivity transition arises only when the intergrain Josephson coupling E(J) is of the order of the thermal energy and phase locking takes place among the superconducting grains. We show that this approach explains the pseudogap and superconducting phases and it also reproduces some recent scanning tunneling microscopy data.

  13. Potential of thermotropic layers to prevent overheating -- A review

    SciTech Connect

    Wilson, H.R.

    1994-12-31

    This paper aims to present a representative rather than exhaustive review of recent research on thermotropic materials, which have the potential for being produced on the large scale required for solar energy system applications. Thermochromic and variably light scattering materials are treated, with brief discussions of the physical switching mechanisms, the spectra of the materials in the low-temperature, high-transmittance and high-temperature, low-transmittance states, long-term stability and system simulation. The integrated values of visible (luminous) and solar transmittance above and below the switching temperature are given to allow a qualitative comparison of the different materials and identification of appropriate applications.

  14. Evolution of a phase separated gravity independent bioreactor

    NASA Astrophysics Data System (ADS)

    Villeneuve, Peter E.; Dunlop, Eric H.

    The evolution of a phase-separated gravity-independent bioreactor is described. The initial prototype, a zero head-space manifold silicone membrane based reactor, maintained large diffusional resistances. Obtaining oxygen transfer rates needed to support carbon-recycling aerobic microbes is impossible if large resistances are maintained. Next generation designs (Mark I and II) mimic heat exchanger design to promote turbulence at the tubing-liquid interface, thereby reducing liquid and gas side diffusional resistances. While oxygen transfer rates increased by a factor of ten, liquid channeling prevented further increases. To overcome these problems, a Mark III reactor was developed which maintains inverted phases, i.e., media flows inside the silicone tubing, oxygen gas is applied external to the tubing. This enhances design through changes in gas side driving force concentration and liquid side turbulence levels. Combining an applied external pressure of four atmospheres with increased Reynolds numbers resulted in oxygen transfer intensities of 232 mmol O2/l/h (1000 times greater than first prototype and comparable to a conventional fermenter). A 1.0 liter Mark III reactor can potentially deliver oxygen supplies necessary to support cell cultures needed to recycle a 10 astronaut carbon load continuously.

  15. Evolution of a phase separated gravity independent bioreactor

    NASA Technical Reports Server (NTRS)

    Villeneuve, Peter E.; Dunlop, Eric H.

    1992-01-01

    The evolution of a phase-separated gravity-independent bioreactor is described. The initial prototype, a zero head-space manifold silicone membrane based reactor, maintained large diffusional resistances. Obtaining oxygen transfer rates needed to support carbon-recycling aerobic microbes is impossible if large resistances are maintained. Next generation designs (Mark I and II) mimic heat exchanger design to promote turbulence at the tubing-liquid interface, thereby reducing liquid and gas side diffusional resistances. While oxygen transfer rates increased by a factor of ten, liquid channeling prevented further increases. To overcome these problems, a Mark III reactor was developed which maintains inverted phases, i.e., media flows inside the silicone tubing, oxygen gas is applied external to the tubing. This enhances design through changes in gas side driving force concentration and liquid side turbulence levels. Combining an applied external pressure of 4 atm with increased Reynolds numbers resulted in oxygen transfer intensities of 232 mmol O2/l per hr (1000 times greater than the first prototype and comparable to a conventional fermenter). A 1.0 liter Mark III reactor can potentially deliver oxygen supplies necessary to support cell cultures needed to recycle a 10-astronaut carbon load continuously.

  16. Phase separation in a polarized Fermi gas with spin-orbit coupling

    SciTech Connect

    Yi, W.; Guo, G.-C.

    2011-09-15

    We study the phase separation of a spin-polarized Fermi gas with spin-orbit coupling near a wide Feshbach resonance. As a result of the competition between spin-orbit coupling and population imbalance, the phase diagram for a uniform gas develops a rich structure of phase separation involving topologically nontrivial gapless superfluid states. We then demonstrate the phase separation induced by an external trapping potential and discuss the optimal parameter region for the experimental observation of the gapless superfluid phases.

  17. DUAL PHASE MEMBRANE FOR HIGH TEMPERATURE CO2 SEPARATION

    SciTech Connect

    Jerry Y.S. Lin; Seungjoon Chung; Matthew Anderson

    2005-12-01

    This project is intended to expand upon the previous year's research en route to the development of a sustainable dual phase membrane for CO{sub 2} separation. It was found that the pores within the supports had to be less than 9 {micro}m in order to maintain the stability of the dual phase membrane. Pores larger than 9 {micro}m would be unable to hold the molten carbonate phase in place, rendering the membrane ineffective. Calculations show that 80% of the pore volume of the 0.5 media grade metal support was filled with the molten carbonate. Information obtained from EDS and SEM confirmed that the molten carbonate completely infiltrated the pores on both the contact and non-contact size of the metal support. Permeation tests for CO{sub 2} and N{sub 2} at 450-750 C show very low permeance of those two gases through the dual phase membrane, which was expected due to the lack of ionization of those two gases. Permeance of the CO{sub 2} and O{sub 2} mixture was much higher, indicating that the gases do form an ionic species, CO{sub 3}{sup 2-}, enhancing transport through the membrane. However, at temperatures in excess of 650 C, the permeance of CO{sub 3}{sup 2-} decreased quite rapidly, while predictions showed that permeance should have continued to increase. XRD data obtained form the surface of the membrane indicated the formation of lithium iron oxides on the support. This layer has a very low conductivity, which drastically reduces the flow of electrons to the CO{sub 2}/O{sub 2} gas mixture, limiting the formation of the ionic species. These results indicate that the use of stainless steel supports in a high temperature oxidative environment can lead to decreased performance of the membranes. This revelation has created the need for an oxidation resistant support, which can be gained by the use of a ceramic-type membrane. Future research efforts will be directed towards preparation of a new ceramic-carbonate dual phase membrane. The membrane will based on an

  18. Ferromagnetic order in silicon-manganese alloys with phase separation

    SciTech Connect

    Men'shov, V. N. Tugushev, V. V.

    2011-07-15

    A phenomenological model of high-temperature ferromagnetism in silicon-manganese alloys has been proposed taking into account phase separation in these alloys, where manganese-rich particles of the secondary phase (precipitate MnSi{sub 2-z} with z Almost-Equal-To 0.25-0.30) are formed inside a manganese-depleted matrix of almost pure silicon. Precipitate MnSi{sub 2-z} is considered as the silicide MnSi{sub 1.7} containing a certain number of magnetic defects whose origin is due to the presence of weakly hybridized 3d orbitals of manganese. The silicide MnSi{sub 1.7} is a weak band ferromagnet in which strong fluctuations of the spin density (paramagnons) are present at a temperature much higher than its Curie temperature. It has been shown that the ferromagnetic exchange interactions between the magnetic moments of defects in precipitate exists due to thermal excitations of the spin density and the ferromagnetic order can appear at a temperature much higher than the Curie temperature of the silicide. The spatial structures and characteristics of this order have been described in the framework of the proposed approach for both homogeneous bulk precipitate and precipitate particles of various shapes and sizes. The short-range magnetic order near the bulk phase transition has been analyzed taking into account inhomogeneities in the distribution of magnetic defects in precipitate. The experimental data on the magnetic properties of silicon-manganese alloys have been interpreted in terms of the theoretical results obtained in this work.

  19. Comparison of liquid and supercritical fluid chromatography mobile phases for enantioselective separations on polysaccharide stationary phases.

    PubMed

    Khater, Syame; Lozac'h, Marie-Anne; Adam, Isabelle; Francotte, Eric; West, Caroline

    2016-10-07

    Analysis and production of enantiomerically pure compounds is a major topic of interest when active pharmaceutical ingredients are concerned. Enantioselective chromatography has become a favourite both at the analytical and preparative scales. High-performance liquid chromatography (HPLC) and supercritical fluid chromatography (SFC) are dominating the scene and are often seen as complementary techniques. Nowadays, for economic and ecologic reasons, SFC may be preferred over normal-phase HPLC (NPLC) as it allows significant reductions in solvent consumption. However, the transfer of NPLC methods to SFC is not always straightforward. In this study, we compare the retention of achiral molecules and separation of enantiomers under supercritical fluid (carbon dioxide with ethanol or isopropanol) and liquid normal-phase (heptane with ethanol or isopropanol) elution modes with polysaccharide stationary phases in order to explore the differences between the retention and enantioseparation properties between the two modes. Chemometric methods (namely quantitative structure-retention relationships and discriminant analysis) are employed to compare the results obtained on a large set of analytes (171 achiral probes and 97 racemates) and gain some understanding on the retention and separation mechanisms. The results indicate that, contrary to popular belief, carbon dioxide - solvent SFC mobile phases are often weaker eluents than liquid mobile phases. It appears that SFC and NPLC elution modes provide different retention mechanisms. While some enantioseparations are unaffected, facilitating the transfer between the two elution modes, other enantioseparations may be drastically different due to different types and strength of interactions contributing to enantioselectivity.

  20. Dual Phase Membrane for High Temperature CO2 Separation

    SciTech Connect

    Jerry Y.S. Lin; Matthew Anderson

    2006-09-29

    Dual-phase membranes consisting of stainless steel supports infiltrated with molten carbonate have been shown to be selective to CO{sub 2} at high temperatures (400-650 C). However, over time at high temperatures, the formation of iron oxides on the surface of the stainless steel supports render the membranes ineffective. This report details synthesis and characteristics of dual-phase carbonate membrane with an oxidation resistant perovskite type ceramic (lanthanum-strontium-cobaltite-iron; LSCF) support. Porous LSCF supports were prepared from its powder synthesized by the citrate method. Both steady state permeation and mercury porosimetry confirmed that the LSCF membrane sintered at 900 C has pores large enough to absorb molten carbonate, yet small enough to retain the molten carbonate under high pressure conditions. Results of XRD analysis have shown that LSCF and the molten carbonate mixture do not react with each other at temperatures below 700 C. Four-point method conductivity tests indicate that the support material has sufficiently high electronic conductivity for this application. Li-Na-K carbonate was coated to the porous LSCF support by a liquid infiltration method. Helium permeance of the support before and after infiltration of molten carbonate are on the order of 10{sup -6} and 10{sup -10} moles/m{sup 2} {center_dot} Pa {center_dot} s respectively, indicating that the molten carbonate is able to sufficiently infiltrate the membrane. Preliminary high temperature permeation experiments indicate that the membrane does separate CO{sub 2} in the presence of O{sub 2}, with a maximum flux of 0.623 ml/cm{sup 2} {center_dot} min obtained at 850 C.

  1. Relation between the phase separation and the crystallization in protein solutions

    NASA Astrophysics Data System (ADS)

    Tanaka, Shinpei; Yamamoto, Masahiko; Ito, Kohzo; Hayakawa, Reinosuke; Ataka, Mitsuo

    1997-07-01

    Liquid-liquid phase separation and crystallization (or solid-liquid phase separation) both occur in protein solutions. By adopting egg-white lysozyme for a model system, we compared two types of diagrams, a phase diagram of the liquid-liquid phase separation and a morphological diagram of protein crystals. By superimposing these diagrams, we distinguished two types of white precipitates, urchinlike spherulites arising from the crystallization and protein-rich droplets from the liquid-liquid phase separation. Furthermore, we observed a transformation from the protein-rich droplets to the spherulites, and simultaneously an unusual pattern evolution of the protein-rich phase unlike the conventional phase separation of typical binary mixtures. This is understood in terms of the competition between the crystallization and the liquid-liquid phase separation.

  2. Amorphous-Amorphous Phase Separation in API/Polymer Formulations.

    PubMed

    Luebbert, Christian; Huxoll, Fabian; Sadowski, Gabriele

    2017-02-15

    The long-term stability of pharmaceutical formulations of poorly-soluble drugs in polymers determines their bioavailability and therapeutic applicability. However, these formulations do not only often tend to crystallize during storage, but also tend to undergo unwanted amorphous-amorphous phase separations (APS). Whereas the crystallization behavior of APIs in polymers has been measured and modeled during the last years, the APS phenomenon is still poorly understood. In this study, the crystallization behavior, APS, and glass-transition temperatures formulations of ibuprofen and felodipine in polymeric PLGA excipients exhibiting different ratios of lactic acid and glycolic acid monomers in the PLGA chain were investigated by means of hot-stage microscopy and DSC. APS and recrystallization was observed in ibuprofen/PLGA formulations, while only recrystallization occurred in felodipine/PLGA formulations. Based on a successful modeling of the crystallization behavior using the Perturbed-Chain Statistical Associating Fluid Theory (PC-SAFT), the occurrence of APS was predicted in agreement with experimental findings.

  3. Nanoscale phase separation in ultra-tough hydrogels

    NASA Astrophysics Data System (ADS)

    Nixon, Ryan; Ten Hove, Jan Bart; Orozco, Adrian; Sawyer, W. Gregory; Angelini, Thomas

    2014-03-01

    Soft, wettable, water permeable materials that resist protein adsorption are essential to countless biomaterials, adaptive optics and microfluidics technologies. Hydrogels would be ideal for these applications, but are notoriously brittle and weak. For example, hydrogel coatings of synovial joint prosthetics exhibit irrecoverable damage after a single cycle of wear. The development of elastomer-like hydrogels that are tough, soft, and mechanically resilient would improve their versatility and create opportunities for a wide range of new applications. Here we present studies of an ultra-tough hydrogel, synthesized by the co-polymerization of two monomer species that polymerize at different rates and have strongly differing degrees of solvation. The resulting blended hydrogel network forms with both covalent and labile adhesive bonds, greatly improving recoverable energy dissipation and reducing fatigue relative to networks made from either constituent alone. We have studied the structural origins of the strengthening behavior using small angle x-ray scattering (SAXS) and found that the constituent polymers phase separate into nanoscale domains, which may prevent crack nucleation and propagation.

  4. Confinement-Driven Phase Separation of Quantum Liquid Mixtures

    NASA Astrophysics Data System (ADS)

    Prisk, T. R.; Pantalei, C.; Kaiser, H.; Sokol, P. E.

    2012-08-01

    We report small-angle neutron scattering studies of liquid helium mixtures confined in Mobil Crystalline Material-41 (MCM-41), a porous silica glass with narrow cylindrical nanopores (d=3.4nm). MCM-41 is an ideal model adsorbent for fundamental studies of gas sorption in porous media because its monodisperse pores are arranged in a 2D triangular lattice. The small-angle scattering consists of a series of diffraction peaks whose intensities are determined by how the imbibed liquid fills the pores. Pure He4 adsorbed in the pores show classic, layer-by-layer film growth as a function of pore filling, leaving the long range symmetry of the system intact. In contrast, the adsorption of He3-He4 mixtures produces a structure incommensurate with the pore lattice. Neither capillary condensation nor preferential adsorption of one helium isotope to the pore walls can provide the symmetry-breaking mechanism. The scattering is consistent with the formation of randomly distributed liquid-liquid microdomains ˜2.3nm in size, providing evidence that confinement in a nanometer scale capillary can drive local phase separation in quantum liquid mixtures.

  5. Carbon Dioxide Separation from Flue Gas by Phase Enhanced Absorption

    SciTech Connect

    Liang Hu

    2006-06-30

    A new process, phase enhanced absorption, was invented. The method is carried out in an absorber, where a liquid carrier (aqueous solution), an organic mixture (or organic compound), and a gas mixture containing a gas to be absorbed are introduced from an inlet. Since the organic mixture is immiscible or at least partially immiscible with the liquid carrier, the organic mixture forms a layer or small parcels between the liquid carrier and the gas mixture. The organic mixture in the absorber improves mass transfer efficiency of the system and increases the absorption rate of the gas. The organic mixture serves as a transportation media. The gas is finally accumulated in the liquid carrier as in a conventional gas-liquid absorption system. The presence of the organic layer does not hinder the regeneration of the liquid carrier or recovery of the gas because the organic layer is removed by a settler after the absorption process is completed. In another aspect, the system exhibited increased gas-liquid separation efficiency, thereby reducing the costs of operation and maintenance. Our study focused on the search of the organic layer or transportation layer to enhance the absorption rate of carbon dioxide. The following systems were studied, (1) CO{sub 2}-water system and CO{sub 2}-water-organic layer system; (2) CO{sub 2}-Potassium Carbonate aqueous solution system and CO{sub 2}-Potassium Carbonate aqueous solution-organic layer system. CO{sub 2}-water and CO{sub 2}-Potassium Carbonate systems are the traditional gas-liquid absorption processes. The CO{sub 2}-water-organic layer and CO{sub 2}-Potassium Carbonate-organic layer systems are the novel absorption processes, phase enhanced absorption. As we mentioned early, organic layer (transportation layer phase) is used for the increase of absorption rate. Our study showed that the absorption rate can be increased by adding the organic layer. However, the enhanced factor is highly depended on the liquid mass transfer

  6. Dual Phase Membrane for High temperature CO2 Separation

    SciTech Connect

    Jerry Y.S. Lin; Matthew Anderson

    2005-12-01

    Research in the previous years in this project found that stainless steel supports are oxidized during high temperature, dual phase membrane separation of carbon dioxide (with oxygen). Consequently, a new material has been sought to alleviate the problems with oxidation. Lanthanum cobaltite oxide is a suitable candidate for the support material in the dual phase membrane due to its oxidation resistance and electronic conductivity. Porous lanthanum cobaltite membranes were prepared via the citrate method, using nitrate metal precursors as the source of La, Sr, Co and Fe. The material was prepared and ground into a powder, which was subsequently pressed into disks for sintering at 900 C. Conductivity measurements were evaluated using the four-probe DC method. Support pore size was determined by helium permeation. Conductivity of the lanthanum cobaltite material was found to be at a maximum of 0.1856 S/cm at 550 C. The helium permeance of the lanthanum cobaltite membranes for this research was on the order of 10{sup -6} moles/m{sup 2} {center_dot} Pa {center_dot} s, proving that the membranes are porous after sintering at 900 C. The average pore size based on steady state helium permeance measurements was found to be between 0.37 and 0.57 {micro}m. The lanthanum cobaltite membranes have shown to have desired porosity, pore size and electric conductivity as the support for the dual-phase membranes. Molten carbonate was infiltrated to the pores of lanthanum cobaltite membranes support. After infiltration with molten carbonate, the helium permeance of the membranes decreased by three orders of magnitude to 10{sup -9} moles/m{sup 2} {center_dot} Pa {center_dot} s. This number, however, is one order of magnitude larger than the room temperate permeance of the stainless steel supports after infiltration with molten carbonate. Optimization of the dip coating process with molten carbonate will be evaluated to determine if lower permeance values can be obtained with the

  7. Effect of OH content on phase separation behavior of soda-silica glasses

    NASA Technical Reports Server (NTRS)

    Neilson, G. F.; Weinberg, M. C.; Smith, G. L.

    1986-01-01

    The kinetics of phase separation in a gel and ordinary soda-silica glass are followed by use of small angle X-ray scattering. Also, the influence of OH on the phase separation behavior is studied. It is found that OH accelerates the growth of the secondary phase, and that gel and ordinary glasses of similar composition and OH concentration exhibit similar phase separation characteristics.

  8. Remote Sensing of Niches for Thermotropic Life.

    NASA Astrophysics Data System (ADS)

    Muller, A. W.

    2002-12-01

    The recognized biological energy sources are light and food. Mechanical systems can gain free energy from heat using a temperature difference or thermal cycling. Imagine that biological systems could also live on heat. Call the process `thermosynthesis' and let it occur in a thermal gradient or convection cell. Many candidate niches for thermosynthesizers then exist. Temperature differences are present across many interfaces: soil/air, rock/air, natural water (ocean, lake, river)/air, ice (also snow)/air, soil/snow, water (ocean,lake)/surface-ice. Within natural waters large temperature gradients are found; thermoclines separate the warm surface from the cold deep. Convection occurs in hot springs, in many other natural waters, and in the Earth's atmosphere. On Earth, organism presence is conspicuous in all these candidate niches. The Solar System contains many candidate niches as well. They should be detectable by IR methods. They can be categorized in five types: (1) Convection. Convecting oceans (Mars and Venus in the past) or atmospheres (Venus, Big Outer Planets). (2) Convecting Aquifer (Mars). (3) Surface-Ice Cover. Some of the Moons of the Outer Planets. (4) Shaded Crater Iterior. The poles of Mercury and The Moon. (5) Spinners. Small objects rotating in the sunlight: ice-covered meteorites, asteroids, comets. They could transport thermosynthesizers within the Solar System. How plausible is thermosynthesis? It can be shown that thermosynthesis (1) could be effected using parts of the contemporary photosynthetic machinery, and (2) may have supported early evolution. The standard biological energy carrier, ATP, would be synthesized during thermal cycling of a progenitor of the F1 moiety of the contemporary ATPsynthase enzyme; this progenitor is thermally folded/unfolded during the cycle. Contemporary ATPsynthase works according to the `binding change mechanism': substrates are bound in a local, dehydrated enzymatic cleft, where they condense to form a bound

  9. Carbon Dioxide Separation from Flue Gas by Phase Enhanced Absorption

    SciTech Connect

    Tim Fout

    2007-06-30

    A new process, phase enhanced absorption, was invented. The method is carried out in an absorber, where a liquid carrier (aqueous solution), an organic mixture (or organic compound), and a gas mixture containing a gas to be absorbed are introduced from an inlet. Since the organic mixture is immiscible or at least partially immiscible with the liquid carrier, the organic mixture forms a layer or small parcels between the liquid carrier and the gas mixture. The organic mixture in the absorber improves mass transfer efficiency of the system and increases the absorption rate of the gas. The organic mixture serves as a transportation media. The gas is finally accumulated in the liquid carrier as in a conventional gas-liquid absorption system. The presence of the organic layer does not hinder the regeneration of the liquid carrier or recovery of the gas because the organic layer is removed by a settler after the absorption process is completed. In another aspect, the system exhibited increased gas-liquid separation efficiency, thereby reducing the costs of operation and maintenance. Our study focused on the search of the organic layer or transportation layer to enhance the absorption rate of carbon dioxide. The following systems were studied, (1) CO{sub 2}-water system and CO{sub 2}-water-organic layer system; (2) CO{sub 2}-Potassium Carbonate aqueous solution system and CO{sub 2}-Potassium Carbonate aqueous solution-organic layer system. CO{sub 2}-water and CO{sub 2}-Potassium Carbonate systems are the traditional gas-liquid absorption processes. The CO{sub 2}-water-organic layer and CO{sub 2}-Potassium Carbonate-organic layer systems are the novel absorption processes, phase enhanced absorption. As we mentioned early, organic layer is used for the increase of absorption rate, and plays the role of transportation of CO{sub 2}. Our study showed that the absorption rate can be increased by adding the organic layer. However, the enhanced factor is highly depended on the

  10. Perylenediimide-surfactant complexes: thermotropic liquid-crystalline materials via ionic self-assembly.

    PubMed

    Guan, Ying; Zakrevskyy, Yuriy; Stumpe, Joachim; Antonietti, Markus; Faul, Charl F J

    2003-04-07

    In this communication we present the facile preparation and characterisation of thermotropic liquid-crystalline materials from the ionic self-assembly of a charged perylenediimide derivative and oppositely charged surfactants.

  11. Fluid Phase Separation (FPS) experiment for flight on a space shuttle Get Away Special (GAS) canister

    NASA Technical Reports Server (NTRS)

    Peters, Bruce; Wingo, Dennis; Bower, Mark; Amborski, Robert; Blount, Laura; Daniel, Alan; Hagood, Bob; Handley, James; Hediger, Donald; Jimmerson, Lisa

    1990-01-01

    The separation of fluid phases in microgravity environments is of importance to environmental control and life support systems (ECLSS) and materials processing in space. A successful fluid phase separation experiment will demonstrate a proof of concept for the separation technique and add to the knowledge base of material behavior. The phase separation experiment will contain a premixed fluid which will be exposed to a microgravity environment. After the phase separation of the compound has occurred, small samples of each of the species will be taken for analysis on the Earth. By correlating the time of separation and the temperature history of the fluid, it will be possible to characterize the process. The experiment has been integrated into space available on a manifested Get Away Special (GAS) experiment, CONCAP 2, part of the Consortium for Materials Complex Autonomous Payload (CAP) Program, scheduled for STS-42. The design and the production of a fluid phase separation experiment for rapid implementation at low cost is presented.

  12. A Temperature-Dependent Phase-Field Model for Phase Separation and Damage

    NASA Astrophysics Data System (ADS)

    Heinemann, Christian; Kraus, Christiane; Rocca, Elisabetta; Rossi, Riccarda

    2017-03-01

    In this paper we study a model for phase separation and damage in thermoviscoelastic materials. The main novelty of the paper consists in the fact that, in contrast with previous works in the literature concerning phase separation and damage processes in elastic media, in our model we encompass thermal processes, nonlinearly coupled with the damage, concentration and displacement evolutions. More particularly, we prove the existence of "entropic weak solutions", resorting to a solvability concept first introduced in uc(Feireisl) (Comput Math Appl 53:461-490, 2007) in the framework of Fourier-Navier-Stokes systems and then recently employed in uc(Feireisl) et al. (Math Methods Appl Sci 32:1345-1369, 2009) and uc(Rocca) and uc(Rossi) (Math Models Methods Appl Sci 24:1265-1341, 2014) for the study of PDE systems for phase transition and damage. Our global-in-time existence result is obtained by passing to the limit in a carefully devised time-discretization scheme.

  13. Crystalline Phase Separation in Phosphate Containing Waste Glasses: Relevance to INEEL HAW

    SciTech Connect

    Jantzen, C.M.

    2000-09-21

    As part of the Tanks Focus Area's (TFA) effort to increase waste loading for high-level waste vitrification at various facilities in the Department of Energy (DOE) complex, the occurrence of phase separation in waste glasses spanning the Savannah River Site (SRS) and Idaho National Engineering and Environmental Laboratory (INEEL) composition ranges have been studied. The type of phase separation that occurs in the phosphate rich borosilicate waste glasses, such as those investigated for INEEL, crystallizes upon cooling. This type of phase separation mechanism is less well studied than amorphous phase separation in phosphate poor borosilicate waste glasses. Therefore, the type of phase separation, extent, and impact of phase separation on glass durability for a series of INEEL-type glasses were examined and the data statistically analyzed in this study.

  14. Interplay between gelation and phase separation in aqueous solutions of methylcellulose and hydroxypropylmethylcellulose.

    PubMed

    Fairclough, J Patrick A; Yu, Hao; Kelly, Oscar; Ryan, Anthony J; Sammler, Robert L; Radler, Michael

    2012-07-17

    Thermally induced gelation in aqueous solutions of methylcellulose (MC) and hydroxypropylmethylcellulose (HPMC) has been studied by rheological, optical microscopy, and turbidimetry measurements. The structural and mechanical properties of these hydrogels are dominated by the interplay between phase separation and gelation. In MC solutions, phase separation takes place almost simultaneously with gelation. An increase in the storage modulus is coupled to the appearance of a bicontinuous structure upon heating. However, a thermal gap exists between phase separation and gelation in the case of HPMC solutions. The storage modulus shows a dramatic decrease during phase separation and then rises in the subsequent gelation. A macroporous structure forms in the gels via "viscoelastic phase separation" linked to "double phase separation".

  15. A computational model for swirl vane phase separators

    NASA Astrophysics Data System (ADS)

    Lider, Serhat

    The main objective of this study is to develop a mechanistic separator-dryer model for the TRAC-BF1 code to solve the problems associated with the modeling of the steam separation phenomena. This model, in a sense, is an extension to the existing separator-dryer model in the TRAC-BF1 code. The phasic velocities and the pressures for the vapor core and the liquid film regions of the swirl vane separator are solved by the use of phasic mass and momentum equations along with pressure drop. A new dryer efficiency model is also introduced. In this model, the dryer efficiency is calculated by the corrugated plate efficiency model. The important part of the study focuses on the implementation of the separator-dryer model to the code. The implementation uses the correct convective parameters in the solution of the conservation equation for the mixing cell of separator-dryer component. The model is tested and assessed against the experimental data, an actual reactor transient, and the results of the existing model. The results indicates that the new steam separation model is more accurate and more robust when compared to the separator-dryer model.

  16. Influence of Simple Electrolytes on the Orientational Ordering of Thermotropic Liquid Crystals at Aqueous Interfaces

    PubMed Central

    Carlton, Rebecca J.; Gupta, Jugal K.; Swift, Candice L.; Abbott, Nicholas L.

    2011-01-01

    We report orientational anchoring transitions at aqueous interfaces of a water-immiscible, thermotropic liquid crystal (LC; nematic phase of 4′-pentyl-4-cyanobiphenyl) that are induced by changes in pH of the aqueous solution and the addition of simple electrolytes (NaCl) to the aqueous phase. Whereas measurements of the zeta potential on the aqueous side of the interface of LC-in-water emulsions prepared with 5CB confirm pH-dependent formation of an electrical double layer extending into the aqueous phase, quantification of the orientational ordering of the LC leads to the proposition that an electrical double layer is also formed on the LC-side of the interface with an internal electric field that drives the LC anchoring transition. Further support for this conclusion is obtained from measurements of the dependence of LC ordering on pH and ionic strength, as well as a simple model based on the Poisson-Boltzmann equation from which we calculate the contribution of an electrical double layer to the orientational anchoring energy of the LC. Overall, the results presented herein provide new fundamental insights into ionic phenomena at LC-aqueous interfaces, and expand the range of solutes known to cause orientational anchoring transitions at LC-aqueous interfaces beyond previously examined amphiphilic adsorbates. PMID:22106820

  17. SANS study of phase separation in solid {sup 3}He-{sup 4}He

    SciTech Connect

    Koster, J.P.; Nagler, S.E.; Adams, E.D.; Wignall, G.D.

    1994-12-31

    Small angle neutron scattering has been used to study phase separation in a quantum alloy, solid {sup 3}He{sub x}-{sup 4}He{sub 1{minus}x}. The onset of phase separation is marked by a dramatic increase in the measured scattering. A simple interpretation of the results suggests that the late-stage phase separation kinetics are dominated by an increase in the concentration of {sup 3}He atoms in preexisting precipitate regions.

  18. Liquid crystal alignment with a molecular template of imprinted polymer layer during phase separation

    NASA Astrophysics Data System (ADS)

    Kim, Hak-Rin; Jung, Jong-Wook; Lee, You-Jin; Kim, Jae-Hoon

    2006-03-01

    We developed a liquid crystal (LC) alignment method using a molecular template of an imprinted polymer layer during polymerization-induced phase separation. Our results showed that the nematic ordering of LC is transferred to the polymer chain ordering during an anisotropic phase separation, which produces an anisotropic azimuthal surface anchoring. Using in-plane field treatment during phase separation, a twisted nematic cell is demonstrated.

  19. Phase separation of integral membrane proteins in Triton X-114 solution.

    PubMed

    Bordier, C

    1981-02-25

    A solution of the nonionic detergent Triton X-114 is homogeneous at 0 degrees C but separates in an aqueous phase and a detergent phase above 20 degrees C. The extent of this detergent phase separation increases with the temperature and is sensitive to the presence of other surfactants. The partition of proteins during phase separation in solutions of Triton X-114 is investigated. Hydrophilic proteins are found exclusively in the aqueous phase, and integral membrane proteins with an amphiphilic nature are recovered in the detergent phase. Triton X-114 is used to solubilize membranes and whole cells, and the soluble material is submitted to phase separation. Integral membrane proteins can thus be separated from hydrophilic proteins and identified as such in crude membrane or cellular detergent extracts.

  20. An improved directional growth apparatus for liquid crystals: applications to thermotropic and lyotropic systems

    NASA Astrophysics Data System (ADS)

    Oswald, P.; Moulin, M.; Metz, P.; Géminard, J. C.; Sotta, P.; Sallen, L.

    1993-09-01

    We have built a directional growth apparatus adapted for the study of thermotropic or lyotropic liquid crystals. This cell allows us to work under inert gas, to orient the sample from outside with respect to the temperature gradient, and to measure the front temperature within 0.1°C. Three applications are described. The first deals with the growth of a monocrystal of pivalic acid when the easy growth axis makes an angle with the heat flow direction. The second experiment is concerned with the fast growth of a discotic liquid crystal and the measurement of the molecular attachment kinetic coefficient at the interface between the columnar hexagonal mesophase and the isotropic liquid. A dynamical anchoring transition between domains of planar and homeotropic orientation will be also described. The last example focuses on the growth of a hexagonal phase of a water-surfactant binary mixture and the first observation of the Mullins-Sekerka instability in a lyotropic system. Nous avons construit une cellule de croissance directionnelle adaptée à l'étude des cristaux liquides thermotropes ou lyotropes. Cette cellule permet de travailler en atmosphère inerte, d'orienter l'échantillon de l'extérieur par rapport au gradient de température, et de mesurer la température du front à 0.1°C près. Trois exemples d'application sont décrits. Le premier porte sur la croissance d'un monocristal d'acide pivalique quand l'axe de croissance facile des cellules fait un angle avec la direction du flux de chaleur. La seconde expérience porte sur la croissance rapide d'un cristal liquide discotique et la mesure du coefficient cinétique d'attachement moléculaire à l'interface entre la mésophase colonnaire hexagonale et le liquide isotrope. Une transition d'ancrage dynamique entre des domaines d'orientations planaire et homéotrope sera également décrite. Le dernier exemple porte sur la croissance d'une phase hexagonale d'un mélange binaire eau-surfactant et la premi

  1. On separability of A-phases during the cyclic alternating pattern.

    PubMed

    Mendez, M O; Alba, A; Chouvarda, I; Milioli, G; Grassi, A; Terzano, M G; Parrino, L

    2014-01-01

    A statistical analysis of the separability of EEG A-phases, with respect to basal activity, is presented in this study. A-phases are short central events that build up the Cyclic Alternating Pattern (CAP) during sleep. The CAP is a brain phenomenon which is thought to be related to the construction, destruction and instability of sleep stages dynamics. From the EEG signals, segments obtained around the onset and offset of the A-phases were used to evaluate the separability between A-phases and basal sleep stage oscillations. In addition, a classifier was trained to separate the different A-phase types (A1, A2 and A3). Temporal, energy and complexity measures were used as descriptors for the classifier. The results show a percentage of separation between onset and preceding basal oscillations higher than 85 % for all A-phases types. For Offset separation from following baseline, the accuracy is higher than 80 % but specificity is around 75%. Concerning to A-phase type separation, A1-phase and A3-phase are well separated with accuracy higher than 80, while A1 and A2-phases show a separation lower than 50%. These results encourage the design of automatic classifiers for Onset detection and for separating among A-phases type A1 and A3. On the other hand, the A-phase Offsets present a smooth transition towards the basal sleep stage oscillations, and A2-phases are very similar to A1-phases, suggesting that a high uncertainty may exist during CAP annotation.

  2. Formation of binary phase gratings in photopolymer-liquid crystal composites by a surface-controlled anisotropic phase separation

    SciTech Connect

    Park, Jae-Hong; Khoo, Iam Choon; Yu, Chang-Jae; Jung, Min-Sik; Lee, Sin-Doo

    2005-01-10

    We report on formation of binary phase gratings in photopolymer-liquid crystal (PLC) composites using a surface-controlled phase separation method. The binary nature of the PLC phase gratings is produced by employing a single step photo-ablation through an amplitude photomask which precisely controls the interfacial interactions between the LC and the photopolymer on the alignment layer. A subsequent illumination of the ultraviolet light onto the whole PLC promotes an anisotropic phase separation resulting in the formation of distinct binary patterns for the PLC structure. The electrically tunable diffraction properties of the binary phase gratings are presented.

  3. Two-phase, passive separator-and-filter assembly

    NASA Technical Reports Server (NTRS)

    Erickson, A. C.; Porter, F. J., Jr.

    1974-01-01

    Assembly separates liquid from gas by passive hydrophilic/hydrophobic material approach. Apparatus is comprised of porous glass hydrophilic tubes. Quantity, lateral size, and pore size of glass tubes are determined by particular design requirements with regard to water rate, water quality contamination level, application endurance life, and operating differential pressure level.

  4. Separations/pretreatment considerations for Hanford privatization phase 2

    SciTech Connect

    Hunt, R.D.; McGinnis, C.P.; Welch, T.D.

    1998-05-01

    The Tank Focus Area is funded to develop, demonstrate, and deploy technologies that will assist in the treatment and closure of its nuclear waste tanks. Pretreatment technologies developed to support the privatization effort by the Department of Energy are reviewed. Advancements in evaporation, solid-liquid separation, sludge treatment, solids controls, sodium management, and radionuclide removal are considered.

  5. Phase separation in lipid bilayers triggered by low pH

    SciTech Connect

    Suresh, Swetha; Edwardson, J. Michael

    2010-09-03

    Research highlights: {yields} Lipid bilayers have been imaged by atomic force microscopy (AFM). {yields} At pH 5 phase separation occurs in lipid bilayers containing mixed acyl chains. {yields} Phase separation does not occur when lipids have only unsaturated chains. {yields} Phase separation might drive protein clustering during endocytosis. -- Abstract: Endocytosis involves the capture of membrane from the cell surface in the form of vesicles, which become rapidly acidified to about pH 5. Here we show using atomic force microscopy (AFM) imaging that this degree of acidification triggers phase separation in lipid bilayers containing mixed acyl chains (e.g. palmitoyl/oleoyl) or complex mixtures (e.g. total brain extract) but not in bilayers containing only lipids with unsaturated chains (e.g. dioleoyl). Since mixed-chain lipids are major constituents of the outer leaflet of the plasma membrane, the type of phase separation reported here might support protein clustering and signaling during endocytosis.

  6. Vertical phase separation in bulk heterojunction solar cells formed by in situ polymerization of fulleride

    PubMed Central

    Zhang, Lipei; Xing, Xing; Zheng, Lingling; Chen, Zhijian; Xiao, Lixin; Qu, Bo; Gong, Qihuang

    2014-01-01

    Vertical phase separation of the donor and the acceptor in organic bulk heterojunction solar cells is crucial to improve the exciton dissociation and charge transport efficiencies. This is because whilst the exciton diffusion length is limited, the organic film must be thick enough to absorb sufficient light. However, it is still a challenge to control the phase separation of a binary blend in a bulk heterojunction device architecture. Here we report the realization of vertical phase separation induced by in situ photo-polymerization of the acrylate-based fulleride. The power conversion efficiency of the devices with vertical phase separation increased by 20%. By optimising the device architecture, the power conversion efficiency of the single junction device reached 8.47%. We believe that in situ photo-polymerization of acrylate-based fulleride is a universal and controllable way to realise vertical phase separation in organic blends. PMID:24861168

  7. Pinning of phase separation of aqueous solution of hydroxypropylmethylcellulose by gelation

    NASA Astrophysics Data System (ADS)

    Kita, Rio; Kaku, Takeshi; Kubota, Kenji; Dobashi, Toshiaki

    1999-08-01

    Opalescence of the aqueous solution of hydroxypropylmethylcellulose (HPMC) induced by heating has been studied in terms of the phase diagram and the phase separation dynamics. The cloud point curve and the sol-to-gel transition curve intersected with each other at about 55 °C. Just above the cloud-point curve at which the spinodal curve has its minimum, a ring-like scattering pattern appeared corresponding to the spinodal decomposition. Temporal growth of the scattering function in the course of phase separation was studied by a time-resolved light scattering technique. The gelation pinned the phase separation (spinodal decomposition) of the aqueous HPMC solution.

  8. Demixing kinetics of phase separated polymer solutions in microgravity. [cell separation

    NASA Technical Reports Server (NTRS)

    Brooks, D. E.; Bamberger, S. B.; Harris, J. M.; Vanalstine, J.; Snyder, R. S.

    1987-01-01

    In preparation for performing cell partitioning in space the demixing behavior of aqueous two phase systems containing dextran and poly(ethylene glycol) in microgravity was modeled with an isopycnic system and studied on aircraft flights and on STS 51-D. In all types of experiments demixing occurs, eventually producing one phase localized around the wall of the container with the other internalized within it. The demixing kinetics were analyzed in each case.

  9. Kinetics of phase separation and coarsening in dilute surfactant pentaethylene glycol monododecyl ether solutions.

    PubMed

    Tanaka, S; Kubo, Y; Yokoyama, Y; Toda, A; Taguchi, K; Kajioka, H

    2011-12-21

    We investigated the phase separation phenomena in dilute surfactant pentaethylene glycol monodedecyl ether (C(12)E(5)) solutions focusing on the growth law of separated domains. The solutions confined between two glass plates were found to exhibit the phase inversion, characteristic of the viscoelastic phase separation; the majority phase (water-rich phase) nucleated as droplets and the minority phase (micelle-rich phase) formed a network temporarily, then they collapsed into an usual sea-island pattern where minority phase formed islands. We found from the real-space microscopic imaging that the dynamic scaling hypothesis did not hold throughout the coarsening process. The power law growth of the domains with the exponent close to 1/3 was observed even though the coarsening was induced mainly by hydrodynamic flow, which was explained by Darcy's law of laminar flow.

  10. Multiple liquid crystal phases of DNA at high concentrations.

    PubMed

    Strzelecka, T E; Davidson, M W; Rill, R L

    1988-02-04

    DNA packaging in vivo is very tight, with volume concentrations approaching 70% w/v in sperm heads, virus capsids and bacterial nucleoids. The packaging mechanisms adopted may be related to the natural tendency of semi-rigid polymers to form liquid crystalline phases in concentrated solutions. We find that DNA forms at least three distinct liquid crystalline phases at concentrations comparable to those in vivo, with phase transitions occurring over relatively narrow ranges of DNA concentration. A weakly birefringent, dynamic, 'precholesteric' mesophase with microscopic textures intermediate between those of a nematic and a true cholesteric phase forms at the lowest concentrations required for phase separation. At slightly higher DNA concentrations, a second mesophase forms which is a strongly birefringent, well-ordered cholesteric phase with a concentration-dependent pitch varying from 2 to 10 micron. At the highest DNA concentrations, a phase forms which is two-dimensionally ordered and resembles smectic phases of thermotropic liquid crystals observed with small molecules.

  11. Controllable Phase Separation by Boc-Modified Lipophilic Acid as a Multifunctional Extractant

    NASA Astrophysics Data System (ADS)

    Tao, Kai; Adler-Abramovich, Lihi; Gazit, Ehud

    2015-12-01

    While phase separation of immiscible liquid-liquid systems has become increasingly significant in diverse areas, the irreversible nature limits their further application in controllable extraction-concentration or capture-release fields. There is a need for the development of simple, efficient and reversible methods for numerous research and industrial extraction and separation applications. We envisioned Boc-modified lipophilic acids as a simple model for such use based on the studies of the multi-phase transitions of Boc-modified supramolecular polymeric systems. Here, we demonstrate that in the presence of Boc-7-aminoheptanoic acid (Boc-7), phase separation occurs in mixtures of miscible organic solvent and water. The separation behavior was confirmed by differential colorimetric development in aqueous and organic phases using methyl orange staining assays. Component substitution experiments verified that the phase separation results from the subtle balance between the aggregation and the solvation forces of Boc-7, and is reversible by adjusting the solution pH. Owing to the intrinsic hydrophobic properties of the organic phase and the hydrogen bonding-forming ability of the carboxyl group of Boc-7, the phase separation system captures and releases Sudan Red, fluorescein, and streptavidin in a controllable manner. Consequently, a reversible and simple phase separation system can be designed as a multifunctional extractant.

  12. Controllable Phase Separation by Boc-Modified Lipophilic Acid as a Multifunctional Extractant

    PubMed Central

    Tao, Kai; Adler-Abramovich, Lihi; Gazit, Ehud

    2015-01-01

    While phase separation of immiscible liquid-liquid systems has become increasingly significant in diverse areas, the irreversible nature limits their further application in controllable extraction-concentration or capture-release fields. There is a need for the development of simple, efficient and reversible methods for numerous research and industrial extraction and separation applications. We envisioned Boc-modified lipophilic acids as a simple model for such use based on the studies of the multi-phase transitions of Boc-modified supramolecular polymeric systems. Here, we demonstrate that in the presence of Boc-7-aminoheptanoic acid (Boc-7), phase separation occurs in mixtures of miscible organic solvent and water. The separation behavior was confirmed by differential colorimetric development in aqueous and organic phases using methyl orange staining assays. Component substitution experiments verified that the phase separation results from the subtle balance between the aggregation and the solvation forces of Boc-7, and is reversible by adjusting the solution pH. Owing to the intrinsic hydrophobic properties of the organic phase and the hydrogen bonding-forming ability of the carboxyl group of Boc-7, the phase separation system captures and releases Sudan Red, fluorescein, and streptavidin in a controllable manner. Consequently, a reversible and simple phase separation system can be designed as a multifunctional extractant. PMID:26627307

  13. Phase separation in garnet solid solutions and its effect on optical properties.

    PubMed

    Kaveh, Shakiba; Tremblay, Clément P; Norhashim, Nurhakimah; Curry, Richard J; Cheetham, Anthony K

    2013-11-26

    Phase behavior is studied in erbium-doped Y3 Al5 O12 (YAG) garnets synthesized by solid-state reactions. High resolution synchrotron XRD and SEM-EDX studies reveal phase separation at an erbium content between 8 and 50 at%, depending upon the processing conditions. Similar results are found in closely-related garnet systems. The phase separation has a striking effect on the optical properties of YAG:Er(3+) .

  14. Separation of piracetam derivatives on polysaccharide-based chiral stationary phases.

    PubMed

    Kažoka, H; Koliškina, O; Veinberg, G; Vorona, M

    2013-03-15

    High-performance liquid chromatography was used for the enantiomeric separation of two chiral piracetam derivatives. The suitability of six commercially available polysaccharide-based chiral stationary phases (CSPs) under normal phase mode for direct enantioseparation has been investigated. The influence of the CSPs as well the nature and content of an alcoholic modifier in the mobile phase on separation and elution order was studied. It was established that CSP Lux Amylose-2 shows high chiral recognition ability towards 4-phenylsubstituted piracetam derivatives.

  15. Phase conversion and interface growth in phase-separated 3He - 4He liquid mixtures

    NASA Astrophysics Data System (ADS)

    Abe, Haruka; Satoh, Takeo; Burmistrov, Serguei N.

    2005-10-01

    We have developed a method for measuring the transmission coefficient of a sound propagating through the interface in phase-separated He3-He4 liquid mixtures. The method and the results are described with discussions by examining the phase-conversion process of He3 quasiparticles driven to flow across the interface. From the data, we have determined the kinetic growth coefficient of the interface, ξ(T,P,ω) , as a function of temperature, pressure, and frequency. The temperature range of the present investigation is about 2-100mK at the pressure mainly around 1bar with sound frequency 9.64, 14.4, and 32.4MHz . The main specific features observed for the kinetic growth coefficient are, as follows: (i) there is a maximum at some temperature Tm(ω) depending on the frequency, (ii) above Tm(ω) , ξ decreases with the increase of temperature as ∝ω5/2T-3 , and (iii) below Tm(ω) , ξ becomes frequency independent and diminishes as a cube of temperature, T3 .

  16. Effects of attractive colloids on the phase separation behaviors of binary polymer blends

    NASA Astrophysics Data System (ADS)

    Zhang, Xinghua; Chen, Yunlin; Qu, Lijian; Yan, Dadong

    2013-08-01

    The attractive colloids are added as fillers to control the phase behaviors of binary polymer blends. Because the colloids attract both components in the blends, aggregates are formed by the colloids coated with both kinds of polymer brushes. The aggregation results in two contradictory effects on the phase separation. First, the formation of aggregate decreases the translational entropy, which promotes the phase separation. On the other hand, the phase separation causes the extra free energy penalty due to the stretch of the chains attaching on the colloids, which prevents the phase separation. Furthermore, as the concentration or adsorbability of the colloids increases the local fluctuations within the aggregates become important. This results in a transition from the macro-phase separation to the micro-phase separation and the existence of the Lifshitz point. All of these effects lead to diverse phase behaviors in the polymer nanocomposites system. In present work, these behaviors are studied theoretically by the random phase approximation in a model system.

  17. In situ imaging and height reconstruction of phase separation processes in polymer blends during spin coating.

    PubMed

    Ebbens, Stephen; Hodgkinson, Richard; Parnell, Andrew J; Dunbar, Alan; Martin, Simon J; Topham, Paul D; Clarke, Nigel; Howse, Jonathan R

    2011-06-28

    Spin coating polymer blend thin films provides a method to produce multiphase functional layers of high uniformity covering large surface areas. Applications for such layers include photovoltaics and light-emitting diodes where performance relies upon the nanoscale phase separation morphology of the spun film. Furthermore, at micrometer scales, phase separation provides a route to produce self-organized structures for templating applications. Understanding the factors that determine the final phase-separated morphology in these systems is consequently an important goal. However, it has to date proved problematic to fully test theoretical models for phase separation during spin coating, due to the high spin speeds, which has limited the spatial resolution of experimental data obtained during the coating process. Without this fundamental understanding, production of optimized micro- and nanoscale structures is hampered. Here, we have employed synchronized stroboscopic illumination together with the high light gathering sensitivity of an electron-multiplying charge-coupled device camera to optically observe structure evolution in such blends during spin coating. Furthermore the use of monochromatic illumination has allowed interference reconstruction of three-dimensional topographies of the spin-coated film as it dries and phase separates with nanometer precision. We have used this new method to directly observe the phase separation process during spinning for a polymer blend (PS-PI) for the first time, providing new insights into the spin-coating process and opening up a route to understand and control phase separation structures.

  18. Thermophysical properties of fluorinated acrylate homopolymers: Mixing and phase separation

    NASA Astrophysics Data System (ADS)

    Roussel, F.; Saidi, S.; Guittard, F.; Geribaldi, S.

    2002-06-01

    The thermophysical properties of fluorinated acrylate homopolymers are investigated by differential scanning calorimetry (DSC) and optical microscopy and discussed in terms of relative lengths of the fluorinated chain and the hydrocarbon spacer between the acrylate moiety and the fluorinated chain. These compounds exhibit an intrinsic microphase-separation (Isotropic+Isotropic morphology) occurring between the fluorinated chains and the acrylate polymer backbone. It is shown that the enthalpy of mixing is a function of the length of the lateral fluorocarbon chains. The thermophysical behaviour of these materials may be regarded as demixed systems exhibiting an Upper Critical Solution Temperature. The photopolymerization process of one of the monomer is studied by isothermal photocalorimetry. High acrylate double-bond conversion and fast curing rates were obtained thus demonstrating the promising use of these materials for coating and film processing applications using UV-curing techniques.

  19. Soft nanostructuring of YBCO Josephson junctions by phase separation.

    PubMed

    Gustafsson, D; Pettersson, H; Iandolo, B; Olsson, E; Bauch, T; Lombardi, F

    2010-12-08

    We have developed a new method to fabricate biepitaxial YBa2 Cu3 O7-δ (YBCO) Josephson junctions at the nanoscale, allowing junctions widths down to 100 nm and simultaneously avoiding the typical damage in grain boundary interfaces due to conventional patterning procedures. By using the competition between the superconducting YBCO and the insulating Y2 BaCuO5 phases during film growth, we formed nanometer sized grain boundary junctions in the insulating Y2 BaCuO5 matrix as confirmed by high-resolution transmission electron microscopy. Electrical transport measurements give clear indications that we are close to probing the intrinsic properties of the grain boundaries.

  20. Formation of ion clusters in the phase separated structures of neutral-charged polymer blends

    NASA Astrophysics Data System (ADS)

    Kwon, Ha-Kyung; Olvera de La Cruz, Monica

    2015-03-01

    Polyelectrolyte blends, consisting of at least one charged species, are promising candidate materials for fuel cell membranes, for their mechanical stability and high selectivity for proton conduction. The phase behavior of the blends is important to understand, as this can significantly affect the performance of the device. The phase behavior is controlled by χN, the Flory-Huggins parameter multiplied by the number of mers, as well as the electrostatic interactions between the charged backbone and the counterions. It has recently been shown that local ionic correlations, incorporated via liquid state (LS) theory, enhance phase separation of the blend, even in the absence of polymer interactions. In this study, we show phase diagrams of neutral-charged polymer blends including ionic correlations via LS theory. In addition to enhanced phase separation at low χN, the blends show liquid-liquid phase separation at high electrostatic interaction strengths. Above the critical strength, the charged polymer phase separates into ion-rich and ion-poor regions, resulting in the formation of ion clusters within the charged polymer phase. This can be shown by the appearance of multiple spinodal and critical points, indicating the coexistence of several charge separated phases. This work was performed under the following financial assistance award 70NANB14H012 from U.S. Department of Commerce, National Institute of Standards and Technology as part of the Center for Hierarchical Materials Design (CHiMaD).

  1. A fuzzy controlled three-phase centrifuge for waste separation

    SciTech Connect

    Parkinson, W.J.; Smith, R.E.; Miller, N.

    1998-02-01

    The three-phase centrifuge technology discussed in this paper was developed by Neal Miller, president of Centech, Inc. The three-phase centrifuge is an excellent device for cleaning up oil field and refinery wastes which are typically composed of hydrocarbons, water, and solids. The technology is unique. It turns the waste into salable oil, reusable water, and landfill-able solids. No secondary waste is produced. The problem is that only the inventor can set up and run the equipment well enough to provide an optimal cleanup. Demand for this device has far exceeded a one man operation. There is now a need for several centrifuges to be operated at different locations at the same time. This has produced a demand for an intelligent control system, one that could replace a highly skilled operator, or at least supplement the skills of a less experienced operator. The control problem is ideally suited to fuzzy logic, since the centrifuge is a highly complicated machine operated entirely by the skill and experience of the operator. A fuzzy control system was designed for and used with the centrifuge.

  2. Cell separations and the demixing of aqueous two phase polymer solutions in microgravity

    NASA Technical Reports Server (NTRS)

    Brooks, Donald E.; Bamberger, Stephan; Harris, J. M.; Van Alstine, James M.

    1991-01-01

    Partition in phase separated aqueous polymer solutions is a cell separation procedure thought to be adversely influenced by gravity. In preparation for performing cell partitioning experiments in space, and to provide general information concerning the demixing of immiscible liquids in low gravity, a series of phase separated aqueous polymer solutions have been flown on two shuttle flights. Fluorocarbon oil and water emulsions were also flown on the second flight. The aqueous polymer emulsions, which in one g demix largely by sedimentation and convection due to the density differences between the phases, demixed more slowly than on the ground and the final disposition of the phases was determined by the wetting of the container wall by the phases. The demixing behavior and kinetics were influenced by the phase volume ratio, physical properties of the systems and chamber wall interaction. The average domain size increased linearly with time as the systems demixed.

  3. Phase behavior and molecular dynamics simulation studies of new aqueous two-phase separation systems induced by HEPES buffer.

    PubMed

    Taha, Mohamed; Khoiroh, Ianatul; Lee, Ming-Jer

    2013-01-17

    Here, for the first time, we show that with addition of a biological buffer, 4-(2-hydroxyethyl)piperazine-1-ethanesulfonic acid (HEPES), into aqueous solutions of tetrahydrofuran (THF), 1,3-dioxolane, 1,4-dioxane, 1-propanol, 2-propanol, tert-butanol, acetonitrile, or acetone, the organic solvent can be excluded from water to form a new liquid phase. The phase diagrams have been determined at ambient temperature. In order to understand why and how a zwitterion solute (HEPES) induced phase separation of the investigated systems, molecular dynamics (MD) simulation studies are performed for HEPES + water + THF system. The MD simulations were conducted for the aqueous mixtures with 12 different compositions. The reliability of the simulation results of HEPES in pure water and beyond the phase separation mixtures was justified by comparing the densities obtained from MD with the experimental values. The simulation results of HEPES in pure THF and in a composition inside the phase separation region were justified qualitatively. Interestingly, all HEPES molecules entirely aggregated in pure THF. This reveals that HEPES is insoluble in pure THF, which is consistent with the experimental results. Even more interestingly, the MD simulation for the mixture with composition inside the phase separation region showed the formation of two phases. The THF molecules are squeezed out from the water network into a new liquid phase. The hydrogen bonds (HBs), HB lifetime, HB Gibbs energy (ΔG), radial distribution functions (RDFs), coordination numbers (CNs), electrostatic interactions, and the van der Waals interactions between the different species have been analyzed. Further, MD simulations for the other phase separation systems by choosing a composition inside the two liquids region for each system were also simulated. Our findings will therefore pave the way for designing new benign separation auxiliary agents.

  4. Phase separation in star-linear polymer mixtures.

    PubMed

    Camargo, Manuel; Likos, Christos N

    2009-05-28

    We study mixtures of star polymers and linear chains in good solvent conditions. We consider the effect of the addition of small chains on the equilibrium structure as well as on the phase behavior of low- and intermediate-functionality star solutions. By using a recently introduced effective cross interaction between stars and chains [C. Mayer and C. N. Likos, Macromolecules 40, 1196 (2007)], we solve the two-component Ornstein-Zernike equation, finding evidence for cluster formation, which is accompanied by a spinodal instability at moderate chain concentrations. The binodal lines are numerically calculated and the dependence of the observed phenomena on functionality, size, and concentrations is rationalized by considering the attractive contribution, which is displayed by the effective, chain-modified star-star interaction potential.

  5. Phase Separation and Crystallization of Hemoglobin C in Transgenic Mouse and Human Erythrocytes

    PubMed Central

    Canterino, Joseph E.; Galkin, Oleg; Vekilov, Peter G.; Hirsch, Rhoda Elison

    2008-01-01

    Individuals expressing hemoglobin C (β6 Glu→Lys) present red blood cells (RBC) with intraerythrocytic crystals that form when hemoglobin (Hb) is oxygenated. Our earlier in vitro liquid-liquid (L-L) phase separation studies demonstrated that liganded HbC exhibits a stronger net intermolecular attraction with a longer range than liganded HbS or HbA, and that L-L phase separation preceded and enhanced crystallization. We now present evidence for the role of phase separation in HbC crystallization in the RBC, and the role of the RBC membrane as a nucleation center. RBC obtained from both human homozygous HbC patients and transgenic mice expressing only human HbC were studied by bright-field and differential interference contrast video-enhanced microscopy. RBC were exposed to hypertonic NaCl solution (1.5–3%) to induce crystallization within an appropriate experimental time frame. L-L phase separation occurred inside the RBC, which in turn enhanced the formation of intraerythrocytic crystals. RBC L-L phase separation and crystallization comply with the thermodynamic and kinetics laws established through in vitro studies of phase transformations. This is the first report, to the best of our knowledge, to capture a temporal view of intraerythrocytic HbC phase separation, crystal formation, and dissolution. PMID:18621841

  6. Comprehensive study on the light shielding potential of thermotropic layers for the development of new materials.

    PubMed

    Gruber, D P; Winkler, G; Resch, K

    2015-01-10

    In recent years thermotropic overheating protection glazings have been the focus for both solar thermal collector technology and architecture. A thermotropic glazing changes its light transmittance from highly transparent to light diffusing upon reaching a certain threshold temperature autonomously and reversibly. In thermotropic systems with fixed domains (TSFD) the scattering domains are embedded in a polymer matrix, which exhibits a sudden change of the refractive index upon reaching a threshold temperature. The aim of the present study was to comprehensively investigate the light shielding characteristics and potential of TSFD materials by applying simulation of light scattering in particle-filled layers. In random walk simulations a variety of parameters were varied systematically, and the effect on the light transmission behavior of TSFD was studied. The calculation steps of the simulation process are shown in detail. The simulations demonstrate that there is great potential for the production of functional materials with high overheating protection efficiency.

  7. Structure and thermotropic behavior of the Staphylococcus aureus lipid lysyl-dipalmitoylphosphatidylglycerol.

    PubMed

    Danner, Sabine; Pabst, Georg; Lohner, Karl; Hickel, Andrea

    2008-03-15

    We have characterized the structural and thermotropic properties of one of the most important lipids in the cell membrane of Staphylococcus aureus, lysyl-dipalmitoylphosphatidylglycerol (lysyl-DPPG). applying differential scanning calorimetry and small- and wide-angle x-ray scattering. Microcalorimetry revealed that under physiological conditions (phosphate buffer, 20 mM NaPi, 130 mM NaCl, pH 7.4), the synthetic lysyl-DPPG resembles the features of the parent dipalmitoylphosphatidylglycerol (DPPG) with respect to its melting behavior. However, in contrast to DPPG, lowering the pH did not significantly affect the main transition temperature ( approximately 40 degrees C) of lysyl-DPPG, which can be explained by its difference in protonization because of the lysine group. X-ray experiments yielded the first information on chain packing and morphology of lysyl-DPPG. We found that lysyl-DPPG forms an interdigitated lamellar phase below the chain-melting transition. This can be explained by the large headgroup area of lysyl-DPPG as a result of its charged lysine group, especially if the headgroup is arranged parallel to the bilayer plane. Additionally, lysyl-DPPG degradation products, such as lysine and free fatty acids, had significant influences on the melting behavior and led to a multicomponent melting transition. Our results indicate that the degradation of lysyl-DPPG takes place mainly during the hydration process but also depends on lipid storage time, pH, and thermal treatment. Detailed temperature-resolved experiments at pH 5.0 demonstrated the formation of a lamellar gel phase with tilted hydrocarbon chains and a ripple phase, coexisting with the interdigitated lysyl-DPPG bilayers.

  8. Applied catastrophic phase inversion: a continuous non-centrifugal phase separation step in biphasic whole-cell biocatalysis.

    PubMed

    Glonke, Sebastian; Sadowski, Gabriele; Brandenbusch, Christoph

    2016-11-01

    Biphasic whole-cell biotransformations are known to be efficient alternatives to common chemical synthesis routes, especially for the production of, e.g. apolar enantiopure organic compounds. They provide high stereoselectivity combined with high product concentrations owing to the presence of an organic phase serving as substrate reservoir and product sink. Industrial implementation suffers from the formation of stable Pickering emulsions caused by the presence of cells. State-of-the-art downstream processing includes inefficient strategies such as excessive centrifugation, use of de-emulsifiers or thermal stress. In contrast, using the catastrophic phase inversion (CPI) phenomenon (sudden switch of emulsion type caused by addition of dispersed phase), Pickering-type emulsions can be destabilized efficiently. Within this work a model system using bis(2-ethylhexyl) phthalate (BEHP) as organic phase in combination with E. coli, JM101 was successfully separated using a continuous mixer settler setup. Compared to the state-of-the-art centrifugal separations, this process allows complete phase separation with no detectable water content or cells in the organic phase with no utilities/additives required. Furthermore, the concentration of the product is not affected by the separation. It is therefore a simple applicable method that can be used for separation of stable Pickering-type emulsions based on the knowledge of the point of inversion.

  9. Hierarchical multiscale hyperporous block copolymer membranes via tunable dual-phase separation.

    PubMed

    Yoo, Seungmin; Kim, Jung-Hwan; Shin, Myoungsoo; Park, Hyungmin; Kim, Jeong-Hoon; Lee, Sang-Young; Park, Soojin

    2015-07-01

    The rational design and realization of revolutionary porous structures have been long-standing challenges in membrane science. We demonstrate a new class of amphiphilic polystyrene-block-poly(4-vinylpyridine) block copolymer (BCP)-based porous membranes featuring hierarchical multiscale hyperporous structures. The introduction of surface energy-modifying agents and the control of major phase separation parameters (such as nonsolvent polarity and solvent drying time) enable tunable dual-phase separation of BCPs, eventually leading to macro/nanoscale porous structures and chemical functionalities far beyond those accessible with conventional approaches. Application of this BCP membrane to a lithium-ion battery separator affords exceptional improvement in electrochemical performance. The dual-phase separation-driven macro/nanopore construction strategy, owing to its simplicity and tunability, is expected to be readily applicable to a rich variety of membrane fields including molecular separation, water purification, and energy-related devices.

  10. Multimodal Responses of Self-Organized Circuitry in Electronically Phase Separated Materials

    SciTech Connect

    Herklotz, Andreas; Guo, Hangwen; Wong, Anthony T.; Lee, Ho Nyung; Rack, Philip D.; Ward, Thomas Z.

    2016-07-13

    When confining an electronically phase we separated manganite film to the scale of its coexisting self-organized metallic and these insulating domains allows resistor-capacitor circuit-like responses while providing both electroresistive and magnetoresistive switching functionality.

  11. HPLC SEPARATION OF CHIRAL ORGANOPHOSPHORUS PESTICIDES ON POLYSACCHARIDE CHIRAL STATIONARY PHASES

    EPA Science Inventory

    High-performance liquid chromatographic separation of the individual enantiomers of 12 organophosphorus pesticides (OPs) were obtained on polysaccharide chiral HPLC columns using an alkane-alcohol mobile phase. The OP pesticides were crotoxyphos, dialifor, dyfonate, fenamiphos, ...

  12. An asymmetric tubular ceramic-carbonate dual phase membrane for high temperature CO2 separation.

    PubMed

    Dong, Xueliang; Ortiz Landeros, José; Lin, Y S

    2013-10-25

    For the first time, a tubular asymmetric ceramic-carbonate dual phase membrane was prepared by a centrifugal casting technique and used for high temperature CO2 separation. This membrane shows high CO2 permeation flux and permeance.

  13. HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC SEPARATION OF THE ENANTIOMERS OF ORGANOPHOSPHORUS PESTICIDES ON POLYSACCHARIDE CHIRAL STATIONARY PHASES

    EPA Science Inventory

    High-performance liquid chromatographic separation of the individual enantiomers of 12 organophosphorus pesticides (OPs) was obtained on polysaccharide enantioselective HPLC columns using alkane-alcohol mobile phase. The OP pesticides were crotoxyphos, dialifor, fonofos, fenamiph...

  14. The effect of liquid-liquid phase separation of glass on the properties and crystallization behavior

    NASA Technical Reports Server (NTRS)

    Li, J. Z.

    1985-01-01

    A theoretical discussion is given of the phase separation mechanism of amorphous materials. This includes nucleus growth, spinoidal decomposition, and nuclei agglomeration and coarsening. Various types of glass are analyzed.

  15. Development of the Two Phase Flow Separator Experiment for a Reduced Gravity Aircraft Flight

    NASA Technical Reports Server (NTRS)

    Golliher, Eric; Gotti, Daniel; Owens, Jay; Gilkey, Kelly; Pham, Nang; Stehno, Philip

    2016-01-01

    The recent hardware development and testing of a reduced gravity aircraft flight experiment has provided valuable insights for the future design of the Two Phase Flow Separator Experiment (TPFSE). The TPFSE is scheduled to fly within the Fluids Integration Rack (FIR) aboard the International Space Station (ISS) in 2020. The TPFSE studies the operational limits of gas and liquid separation of passive cyclonic separators. A passive cyclonic separator utilizes only the inertia of the incoming flow to accomplish the liquid-gas separation. Efficient phase separation is critical for environmental control and life support systems, such as recovery of clean water from bioreactors, for long duration human spaceflight missions. The final low gravity aircraft flight took place in December 2015 aboard NASA's C9 airplane.

  16. Smoothed particle hydrodynamics model for phase separating fluid mixtures. II. Diffusion in a binary mixture.

    PubMed

    Thieulot, Cedric; Janssen, L P B M; Español, Pep

    2005-07-01

    A previously formulated smoothed particle hydrodynamics model for a phase separating mixture is tested for the case when viscous processes are negligible and only mass and energy diffusive processes take place. We restrict ourselves to the case of a binary mixture that can exhibit liquid-liquid phase separation. The thermodynamic consistency of the model is assessed and the potential of the model to study complex pattern formation in the presence of various thermal boundaries is illustrated.

  17. Phase Separation of Binary Charged Particle Systems with Small Size Disparities using a Dusty Plasma.

    PubMed

    Killer, Carsten; Bockwoldt, Tim; Schütt, Stefan; Himpel, Michael; Melzer, André; Piel, Alexander

    2016-03-18

    The phase separation in binary mixtures of charged particles has been investigated in a dusty plasma under microgravity on parabolic flights. A method based on the use of fluorescent dust particles was developed that allows us to distinguish between particles of slightly different size. A clear trend towards phase separation even for smallest size (charge) disparities is observed. The diffusion flux is directly measured from the experiment and uphill diffusion coefficients have been determined.

  18. Kinetic model of phase separation in binary mixtures with hard mobile impurities.

    PubMed

    Ginzburg, V V; Peng, G; Qiu, F; Jasnow, D; Balazs, A C

    1999-10-01

    We develop a mean-field rate-equation model for the kinetics of phase separation in binary mixtures with hard mobile impurities. For impurities preferentially wet by one of the components, the phase separation is arrested in the late stage. The "steady-state" domain size depends strongly on both the particle diffusion constant and the particle concentration. We compare theoretical results with the simulation data and find good qualitative agreement.

  19. Use of Solid Phase Extraction in the Biochemistry Laboratory to Separate Different Lipids

    ERIC Educational Resources Information Center

    Flurkey, William H.

    2005-01-01

    Solid-phase extraction (SPE) was used to demonstrate how various lipids and lipid classes could be separated in a biochemistry laboratory setting. Three different SPE methods were chosen on their ability to separate a lipid mixture, consisting of a combination of a either a fatty acid, a triacylglycerol, a mono- or diacylglycerol, phospholipid,…

  20. Fabrication of Janus droplets by evaporation driven liquid-liquid phase separation.

    PubMed

    Zhang, Qingquan; Xu, Meng; Liu, Xiaojun; Zhao, Wenfeng; Zong, Chenghua; Yu, Yang; Wang, Qi; Gai, Hongwei

    2016-04-11

    We present a universal and scalable method to fabricate Janus droplets based on evaporation driven liquid-liquid phase separation. In this work, the morphologies and chemical properties of separate parts of the Janus droplets can be flexibly regulated, and more complex Janus droplets (such as core-shell Janus droplets, ternary Janus droplets, and multiple Janus droplets) can be constructed easily.

  1. Suppression of turbulent energy cascade due to phase separation in homogenous binary mixture fluid

    NASA Astrophysics Data System (ADS)

    Takagi, Youhei; Okamoto, Sachiya

    2015-11-01

    When a multi-component fluid mixture becomes themophysically unstable state by quenching from well-melting condition, phase separation due to spinodal decomposition occurs, and a self-organized structure is formed. During phase separation, free energy is consumed for the structure formation. In our previous report, the phase separation in homogenous turbulence was numerically simulated and the coarsening process of phase separation was discussed. In this study, we extended our numerical model to a high Schmidt number fluid corresponding to actual polymer solution. The governing equations were continuity, Navier-Stokes, and Chan-Hiliard equations as same as our previous report. The flow filed was an isotropic homogenous turbulence, and the dimensionless parameters in the Chan-Hilliard equation were estimated based on the thermophysical condition of binary mixture. From the numerical results, it was found that turbulent energy cascade was drastically suppressed in the inertial subrange by phase separation for the high Schmidt number flow. By using the identification of turbulent and phase separation structure, we discussed the relation between total energy balance and the structures formation processes. This study is financially supported by the Grand-in-Aid for Young Scientists (B) (No. T26820045) from the Ministry of Education, Cul-ture, Sports, Science and Technology of Japan.

  2. Phase separation induced molecular fractionation of gum arabic--sugar beet pectin systems.

    PubMed

    Mao, Peng; Zhao, Meng; Zhang, Fan; Fang, Yapeng; Phillips, Glyn O; Nishinari, Katsuyoshi; Jiang, Fatang

    2013-10-15

    This paper investigates the phase separation and phase separation-induced fractionation of gum arabic (GA)/sugar beet pectin (SBP) mixed solutions. A phase diagram, including cloud and binodal curves, was established by visual observation and phase composition analysis. The deviation of the binodal curve from the cloud curve was a result of phase separation-induced fractionation of polydisperse GA and SBP molecules. Fractionation of GA increased the content of arabinogalactan-protein complex (AGP) from ca. 13% to 27%. The fractionated GA (FGA) showed improved emulsifying functionality, whereas the fractionated SBP (FSBP) had a reduced emulsifying functionality. The changes in emulsifying efficiency can be explained by interfacial adsorption behaviors at the oil-water interface as indicated by interfacial tension measurements.

  3. Images reveal that atmospheric particles can undergo liquid-liquid phase separations

    NASA Astrophysics Data System (ADS)

    Bertram, A. K.; You, Y.; Renbaum-Wolff, L.; Carreras-Sospedra, M.; Hiranuma, N.; Smith, M.; Zhang, X.; Weber, R.; Shilling, J. E.; Dabdub, D.; Martin, S. T.

    2012-12-01

    A large fraction of submicron atmospheric particles contain both organic material and inorganic salts. As the relative humidity cycles in the atmosphere, these mixed particles can undergo a range of phase transitions, possibly including liquid-liquid phase separation. If liquid-liquid phase separation occurs, the gas-particle partitioning of atmospheric semi-volatile organic compounds, the scattering and absorption of solar radiation, and the uptake of reactive gas species on atmospheric particles may be affected. Here, using optical and fluorescence microscopy, we present images that show the coexistence of two non-crystalline phases in particles generated from samples collected on multiple days in Atlanta, Georgia, and in particles generated in the laboratory using simulated atmospheric conditions. These results show that atmospheric particles can undergo liquid-liquid phase separations.

  4. Phase separation of cesium from lead borosilicate glass by heat treatment under a reducing atmosphere.

    PubMed

    Xu, Zhanglian; Okada, Takashi; Nishimura, Fumihiro; Yonezawa, Susumu

    2016-11-05

    A phase-separation technique for removing sodium from glass using a heat-treatment method under a reducing atmosphere was previously developed for sodium recovery from waste glass. In this study, this technique was applied to cesium-containing lead borosilicate glass to concentrate the cesium in phase-separated sodium-rich materials for efficient cesium extraction. The theoretical phase-separation temperature of the sodium-rich phase was simulated by thermodynamic equilibrium calculations and was predicted to occur below 700°C for lead borosilicate glass. Experimentally, a simulated lead borosilicate glass was melted at 1000°C and subsequently annealed below 700°C under a CO-containing reducing atmosphere. The phase separation of cesium was found to occur with sodium enrichment on the glass surface that was in contact with the gas phase, promoting cesium extraction from the treated glass using water. The cesium extraction efficiency was affected by the surface area of the treated glass that was in contact with water, and under the examined conditions, the cesium extraction efficiency was up to 66%. Phase separation using reductive heat treatment, combined with a water leaching technique, is suggested to be effective for extracting cesium incorporated in borosilicate glass waste.

  5. Self-Organisation, Thermotropic and Lyotropic Properties of Glycolipids Related to their Biological Implications

    PubMed Central

    Garidel, Patrick; Kaconis, Yani; Heinbockel, Lena; Wulf, Matthias; Gerber, Sven; Munk, Ariane; Vill, Volkmar; Brandenburg, Klaus

    2015-01-01

    Glycolipids are amphiphilic molecules which bear an oligo- or polysaccharide as hydrophilic head group and hydrocarbon chains in varying numbers and lengths as hydrophobic part. They play an important role in life science as well as in material science. Their biological and physiological functions are quite diverse, ranging from mediators of cell-cell recognition processes, constituents of membrane domains or as membrane-forming units. Glycolipids form an exceptional class of liquid-crystal mesophases due to the fact that their self-organisation obeys more complex rules as compared to classical monophilic liquid-crystals. Like other amphiphiles, the supra-molecular structures formed by glycolipids are driven by their chemical structure; however, the details of this process are still hardly understood. Based on the synthesis of specific glycolipids with a clearly defined chemical structure, e.g., type and length of the sugar head group, acyl chain linkage, substitution pattern, hydrocarbon chain lengths and saturation, combined with a profound physico-chemical characterisation of the formed mesophases, the principles of the organisation in different aggregate structures of the glycolipids can be obtained. The importance of the observed and formed phases and their properties are discussed with respect to their biological and physiological relevance. The presented data describe briefly the strategies used for the synthesis of the used glycolipids. The main focus, however, lies on the thermotropic as well as lyotropic characterisation of the self-organised structures and formed phases based on physico-chemical and biophysical methods linked to their potential biological implications and relevance. PMID:26464591

  6. Enantiomeric separation of biaryl atropisomers using cyclofructan based chiral stationary phases.

    PubMed

    Woods, Ross M; Patel, Darshan C; Lim, Yeeun; Breitbach, Zachary S; Gao, Hongyin; Keene, Craig; Li, Gongqiang; Kürti, László; Armstrong, Daniel W

    2014-08-29

    Normal phase chiral HPLC methods are presented for the enantiomeric separation of 30 biaryl atropisomers including 18 new compounds recently produced via a novel synthetic approach. Three new cyclofructan based chiral stationary phases were evaluated. Separations were achieved for all but six analytes and the LARIHC™ CF6-P alone provided 15 baseline separations. Effects of polar modifiers and temperature effects also were studied. Apparent thermodynamic parameters were determined by van't Hoff plots. Preparative scale methods were developed and employed resulting in the first ever isolation of these novel atropisomers in their pure enantiomeric form. Insights into the mechanism of retention and chiral discrimination are presented.

  7. Enantiomeric Separation of Biaryl Atropisomers Using Cyclofructan Based Chiral Stationary Phases

    PubMed Central

    Woods, Ross M.; Patel, Darshan C.; Lim, Yeeun; Breitbach, Zachary S.; Gao, Hongyin; Keene, Craig; Li, Gongqiang; Kürti, László

    2014-01-01

    Normal phase chiral HPLC methods are presented for the enantiomeric separation of 30 biaryl atropisomers including 18 new compounds recently produced via a novel synthetic approach. Three new cyclofructan based chiral stationary phases were evaluated. Separations were achieved for all but six analytes and the LARIHC™ CF6-P alone provided 15 baseline separations. Effects of polar modifiers and temperature effects also were studied. Apparent thermodynamic parameters were determined by van't Hoff plots. Preparative scale methods were developed and employed resulting in the first ever isolation of these novel atropisomers in their pure enantiomeric form. Insights into the mechanism of retention and chiral discrimination are presented. PMID:24835594

  8. The Two-Phase Flow Separator Experiment Breadboard Model: Reduced Gravity Aircraft Results

    NASA Technical Reports Server (NTRS)

    Rame, E; Sharp, L. M.; Chahine, G.; Kamotani, Y.; Gotti, D.; Owens, J.; Gilkey, K.; Pham, N.

    2015-01-01

    Life support systems in space depend on the ability to effectively separate gas from liquid. Passive cyclonic phase separators use the centripetal acceleration of a rotating gas-liquid mixture to carry out phase separation. The gas migrates to the center, while gas-free liquid may be withdrawn from one of the end plates. We have designed, constructed and tested a breadboard that accommodates the test sections of two independent principal investigators and satisfies their respective requirements, including flow rates, pressure and video diagnostics. The breadboard was flown in the NASA low-gravity airplane in order to test the system performance and design under reduced gravity conditions.

  9. Effect of confinement and kinetics on the morphology of phase separating gelatin-maltodextrin droplets.

    PubMed

    Fransson, Sophia; Lorén, Niklas; Altskär, Annika; Hermansson, Anne-Marie

    2009-06-08

    The effect of confinement on the structure evolution and final morphology during phase separation and gelation of gelatin and maltodextrin was investigated and compared to the structures seen in bulk phase. Emulsion droplets with diameters from 4 to 300 mum were analyzed using confocal laser scanning microscopy and image analysis. With the confocal laser scanning microscope it was possible to follow the entire phase separating process inside the droplets in real-time. The samples were either quenched directly from 70 degrees C down to 20 degrees C or exposed to holding times at 40 degrees C. Different cooling procedures were studied to examine the structure evolution both before and after gelation in the restricted geometries. The concentration of the biopolymer mixture was kept constant at 4 w/w% gelatin and 6 w/w% maltodextrin. The results revealed that the size of the confinement had a great effect on both the initiation of phase separation and the final morphology of the microstructure inside the emulsion droplets. The phase separation in small droplets was observed to occur at a temperature above the phase separating temperature for bulk. Small droplets had either a microstructure with a shell of maltodextrin and core of gelatin or a microstructure where the two biopolymers had formed two separate bicontinuous halves. The initiation of phase separation in large droplets was similar to what was seen in bulk. The microstructure in large droplets was discontinuous, resembling the morphology in bulk phase. The kinetics had an effect on the character of the maltodextrin inclusions, as the cooling procedure of a direct quench gave spherical inclusions with an even size distribution, while a holding time at 40 degrees C resulted in asymmetrical and elongated inclusions.

  10. Extent and mechanism of phase separation during the extrusion of calcium phosphate pastes.

    PubMed

    O'Neill, Rory; McCarthy, Helen O; Cunningham, Eoin; Montufar, Edgar; Ginebra, Maria-Pau; Wilson, D Ian; Lennon, Alex; Dunne, Nicholas

    2016-02-01

    The aim of this study was to increase understanding of the mechanism and dominant drivers influencing phase separation during ram extrusion of calcium phosphate (CaP) paste for orthopaedic applications. The liquid content of extrudate was determined, and the flow of liquid and powder phases within the syringe barrel during extrusion were observed, subject to various extrusion parameters. Increasing the initial liquid-to-powder mass ratio, LPR, (0.4-0.45), plunger rate (5-20 mm/min), and tapering the barrel exit (45°-90°) significantly reduced the extent of phase separation. Phase separation values ranged from (6.22 ± 0.69 to 18.94 ± 0.69 %). However altering needle geometry had no significant effect on phase separation. From powder tracing and liquid content determination, static zones of powder and a non-uniform liquid distribution was observed within the barrel. Measurements of extrudate and paste LPR within the barrel indicated that extrudate LPR remained constant during extrusion, while LPR of paste within the barrel decreased steadily. These observations indicate the mechanism of phase separation was located within the syringe barrel. Therefore phase separation can be attributed to either; (1) the liquid being forced downstream by an increase in pore pressure as a result of powder consolidation due to the pressure exerted by the plunger or (2) the liquid being drawn from paste within the barrel, due to suction, driven by dilation of the solids matrix at the barrel exit. Differentiating between these two mechanisms is difficult; however results obtained suggest that suction is the dominant phase separation mechanism occurring during extrusion of CaP paste.

  11. Polymerization- and solvent-induced phase separation in hydrophilic-rich dentin adhesive mimic.

    PubMed

    Abedin, Farhana; Ye, Qiang; Good, Holly J; Parthasarathy, Ranganathan; Spencer, Paulette

    2014-07-01

    Current dental resin undergoes phase separation into hydrophobic-rich and hydrophilic-rich phases during infiltration of the over-wet demineralized collagen matrix. Such phase separation undermines the integrity and durability of the bond at the composite/tooth interface. This study marks the first time that the polymerization kinetics of model hydrophilic-rich phase of dental adhesive has been determined. Samples were prepared by adding varying water content to neat resins made from 95 and 99 wt.% hydroxyethylmethacrylate and 5 and 1 wt.% (2,2-bis[4-(2-hydroxy-3-methacryloxypropoxy)phenyl1]-propane prior to light curing. Viscosity of the formulations decreased with increased water content. The photopolymerization kinetics study was carried out with a time-resolved Fourier transform infrared spectrometer. All of the samples exhibited two-stage polymerization behavior which has not been reported previously for dental resin formulation. The lowest secondary rate maxima were observed for water contents of 10-30 wt.%. Differential scanning calorimetry (DSC) showed two glass transition temperatures for the hydrophilic-rich phase of dental adhesive. The DSC results indicate that the heterogeneity within the final polymer structure decreased with increasing water content. The results suggest a reaction mechanism involving both polymerization-induced phase separation and solvent-induced phase separation for the model hydrophilic-rich phase of dental resin.

  12. Development of phase-separated scintillators with light-guiding properties.

    PubMed

    Yasui, Nobuhiro; Ohashi, Yoshihiro; Kobayashi, Tamaki; Den, Tohru

    2012-10-23

    Alkali halide systems that function as phase-separated scintillators (PSSs) with light-guiding properties are sucessfully created. Furthermore, it is the matrix phases of the PSSs which display the light-guiding properties. CsI-NaCl:Tl is a practical material pair because of its high pixel light output and good spatial resolution.

  13. Phase separation in the two-dimensional bosonic Hubbard model with ring exchange.

    PubMed

    Rousseau, V; Batrouni, G G; Scalettar, R T

    2004-09-10

    We show that soft-core bosons in two dimensions with a ring exchange term exhibit a tendency for phase separation. This observation suggests that the thermodynamic stability of normal Bose liquid phases driven by ring exchange should be carefully examined.

  14. Double-antibody solid-phase radioimmunoassay: a simplified phase-separation procedure applied to various ligands

    SciTech Connect

    Tevaarwerk, G.J.M.; Boyle, D.A.; Hurst, C.J.; Anguish, I.; Uksik, P.

    1980-06-01

    The purpose was to develop a simplified and reliable method of separating free from antibody-bound ligand using a precipitating antibody linked to a cellulose derivative. Dose-response curves and control sera were set up in parallel for various pituitary and placental polypeptides, steroid hormones, insulin, glucagon, triiodothyronine, thyroxine, angiotensin I, calcitonin, gastrin, cyclic AMP, and digoxin. After first-antibody reactions had reached equilibrium, free and bound ligand were separated using a double-antibody solid-phase system in parallel with conventional methods, including dextran-coated charcoal, double-antibody precipitation, single-antibody solid phase, organic solvents, salt precipitation, and anion-exchange resins. The effect of variations in temperature, incubation time, protein content, pH, and amount of separating material added were studied. The results showed that separation was complete within 1 hr for small ligand molecules and within 2 hr for larger ones. Dose-response curves and control-sera results closely paralleled those obtained with conventional methods. The method was not affected by moderate variations in incubation variables. Nonspecific binding was less than 3% in all assays, while intra-assay and interassay coefficients of variation were similar to those obtained with conventional phase-separation methods. It is concluded that the method is a simple and rapid alternative phase-separation system. It has the advantage of being free from common nonspecific intersample variations, and can be applied to any assay system based on rabbit or guinea pig antibodies without preliminay time- or reagent-consuming titration or adjustments to establish optimum phase-separating conditions.

  15. Liquid-liquid phase separation of freely falling undercooled ternary Fe-Cu-Sn alloy

    PubMed Central

    Wang, W .L.; Wu, Y. H.; Li, L. H.; Zhai, W.; Zhang, X. M.; Wei, B.

    2015-01-01

    The active modulation and control of the liquid phase separation for high-temperature metallic systems are still challenging the development of advanced immiscible alloys. Here we present an attempt to manipulate the dynamic process of liquid-liquid phase separation for ternary Fe47.5Cu47.5Sn5 alloy. It was firstly dispersed into numerous droplets with 66 ~ 810 μm diameters and then highly undercooled and rapidly solidified under the containerless microgravity condition inside drop tube. 3-D phase field simulation was performed to explore the kinetic evolution of liquid phase separation. Through regulating the combined effects of undercooling level, phase separation time and Marangoni migration, three types of separation patterns were yielded: monotectic cell, core shell and dispersive structures. The two-layer core-shell morphology proved to be the most stable separation configuration owing to its lowest chemical potential. Whereas the monotectic cell and dispersive microstructures were both thermodynamically metastable transition states because of their highly active energy. The Sn solute partition profiles of Fe-rich core and Cu-rich shell in core-shell structures varied only slightly with cooling rate. PMID:26552711

  16. Liquid-liquid phase separation of freely falling undercooled ternary Fe-Cu-Sn alloy.

    PubMed

    Wang, W L; Wu, Y H; Li, L H; Zhai, W; Zhang, X M; Wei, B

    2015-11-10

    The active modulation and control of the liquid phase separation for high-temperature metallic systems are still challenging the development of advanced immiscible alloys. Here we present an attempt to manipulate the dynamic process of liquid-liquid phase separation for ternary Fe47.5Cu47.5Sn5 alloy. It was firstly dispersed into numerous droplets with 66 ~ 810 μm diameters and then highly undercooled and rapidly solidified under the containerless microgravity condition inside drop tube. 3-D phase field simulation was performed to explore the kinetic evolution of liquid phase separation. Through regulating the combined effects of undercooling level, phase separation time and Marangoni migration, three types of separation patterns were yielded: monotectic cell, core shell and dispersive structures. The two-layer core-shell morphology proved to be the most stable separation configuration owing to its lowest chemical potential. Whereas the monotectic cell and dispersive microstructures were both thermodynamically metastable transition states because of their highly active energy. The Sn solute partition profiles of Fe-rich core and Cu-rich shell in core-shell structures varied only slightly with cooling rate.

  17. Hierarchical multiscale hyperporous block copolymer membranes via tunable dual-phase separation

    PubMed Central

    Yoo, Seungmin; Kim, Jung-Hwan; Shin, Myoungsoo; Park, Hyungmin; Kim, Jeong-Hoon; Lee, Sang-Young; Park, Soojin

    2015-01-01

    The rational design and realization of revolutionary porous structures have been long-standing challenges in membrane science. We demonstrate a new class of amphiphilic polystyrene-block-poly(4-vinylpyridine) block copolymer (BCP)–based porous membranes featuring hierarchical multiscale hyperporous structures. The introduction of surface energy–modifying agents and the control of major phase separation parameters (such as nonsolvent polarity and solvent drying time) enable tunable dual-phase separation of BCPs, eventually leading to macro/nanoscale porous structures and chemical functionalities far beyond those accessible with conventional approaches. Application of this BCP membrane to a lithium-ion battery separator affords exceptional improvement in electrochemical performance. The dual-phase separation–driven macro/nanopore construction strategy, owing to its simplicity and tunability, is expected to be readily applicable to a rich variety of membrane fields including molecular separation, water purification, and energy-related devices. PMID:26601212

  18. Phase-separation perspective on dynamic heterogeneities in glass-forming liquids.

    PubMed

    Cammarota, C; Cavagna, A; Giardina, I; Gradenigo, G; Grigera, T S; Parisi, G; Verrocchio, P

    2010-07-30

    We study dynamic heterogeneities in a model glass former whose overlap with a reference configuration is constrained to a fixed value. We find that the system phase separates into regions of small and large overlap, indicating that a nonzero surface tension plays an important role in the formation of dynamical heterogeneities. We calculate an appropriate thermodynamic potential and find evidence of a Maxwell construction consistent with a spinodal decomposition of two phases. Our results suggest that even in standard, unconstrained systems dynamic heterogeneities are the expression of an ephemeral phase-separating regime ruled by a finite surface tension.

  19. Laser-induced separation of hydrogen isotopes in the liquid phase

    DOEpatents

    Freund, Samuel M.; Maier, II, William B.; Beattie, Willard H.; Holland, Redus F.

    1980-01-01

    Hydrogen isotope separation is achieved by either (a) dissolving a hydrogen-bearing feedstock compound in a liquid solvent, or (b) liquefying a hydrogen-bearing feedstock compound, the liquid phase thus resulting being kept at a temperature at which spectral features of the feedstock relating to a particular hydrogen isotope are resolved, i.e., a clear-cut isotope shift is delineated, irradiating the liquid phase with monochromatic radiation of a wavelength which at least preferentially excites those molecules of the feedstock containing a first hydrogen isotope, inducing photochemical reaction in the excited molecules, and separating the reaction product containing the first isotope from the liquid phase.

  20. Structure and Phase Separation in Ultrathin Ag/Cu Amorphous Alloy System

    NASA Astrophysics Data System (ADS)

    Chen, Hao

    2005-03-01

    The structure of disordered metallic alloys is an important but unsolved problem. Previous studies on Ag-Cu system showed that relatively homogeneous solid solutions formed at liquid nitrogen temperature decompose into separate phases or evolve into crystalline structure at a higher temperature. In this research project, we prepared ultra-thin Ag-Cu films on amorphous carbon support by HV magnetron sputtering with both targets. With high energy Ag and Cu atoms bombarding on the carbon substrate, they are forced to form amorphous alloy or nano-crystalline thin film at room temperature. We have investigated the structure of ultra-thin Ag-Cu films by examining their pair distribution function (PDF) using electron diffraction and observed phase separation process directly in STEM images. In the STEM Z-contrast images, since the contrast is directly related to the atomic number (Z) of the components, we can see clearly the phase separation process. Experimental results show that the sample morphology evolutions are different in samples with different thickness, and the phase separation depends on various Ag/Cu atomic ratios. In Ag50Cu50 sample, early stage phase separation is associated with increasing Cu crystallite size, indicates that Cu diffuse out of Ag-Cu solid solution phase.

  1. Chiral separation of novel diazenes on a polysaccharide-based stationary phase in the reversed-phase mode.

    PubMed

    Vojtylová, Terézia; Hamplová, Věra; Galewski, Zbigniew; Korbecka, Izabela; Sýkora, David

    2017-01-31

    Chiral high-performance liquid chromatography separation of two recently synthesized liquid crystalline materials C1 and C2 was studied in the reversed-phase mode. Both materials have an azo-moiety and one chiral centre in their molecular structures. They were available in racemic and pure S forms. For the enantiomeric separations, a Chiralpak AY-RH stationary phase based on amylose tris(5-chloro-2-methylphenylcarbamate) coated on 5 μm silica was used. The compounds were analyzed in both of their possible forms, the more thermodynamically stable E form and the labile Z form. The conditions and time scale of the UV-induced E to Z transition were briefly evaluated. Under the optimized conditions, we were able to baseline separate S and R enantiomers of both of the studied materials not only in their E forms but also in their Z forms. In comparison to the separation in the normal-phase mode, which we have reported recently, the resolution in the reversed-phase mode is significantly better. Interestingly, peak reversal was noticed for the S and R enantiomers when the separation was carried out with E versus Z forms of both compounds. This article is protected by copyright. All rights reserved.

  2. Precipitation phase separation schemes in the Naqu River basin, eastern Tibetan plateau

    NASA Astrophysics Data System (ADS)

    Liu, Shaohua; Yan, Denghua; Qin, Tianling; Weng, Baisha; Lu, Yajing; Dong, Guoqiang; Gong, Boya

    2016-11-01

    Precipitation phase has a profound influence on the hydrological processes in the Naqu River basin, eastern Tibetan plateau. However, there are only six meteorological stations with precipitation phase (rainfall/snowfall/sleet) before 1979 within and around the basin. In order to separate snowfall from precipitation, a new separation scheme with S-shaped curve of snowfall proportion as an exponential function of daily mean temperature was developed. The determinations of critical temperatures in the single/two temperature threshold (STT/TTT2) methods were explored accordingly, and the temperature corresponding to the 50 % snowfall proportion (SP50 temperature) is an efficiently critical temperature for the STT, and two critical temperatures in TTT2 can be determined based on the exponential function and SP50 temperature. Then, different separation schemes were evaluated in separating snowfall from precipitation in the Naqu River basin. The results show that the S-shaped curve methods outperform other separation schemes. Although the STT and TTT2 slightly underestimate and overestimate the snowfall when the temperature is higher and colder than SP50 temperature respectively, the monthly and annual separation snowfalls are generally consistent with the observed snowfalls. On the whole, S-shaped curve methods, STT, and TTT2 perform well in separating snowfall from precipitation with the Pearson correlation coefficient of annual separation snowfall above 0.8 and provide possible approaches to separate the snowfall from precipitation for hydrological modelling.

  3. Lower critical solution temperature (LCST) phase separation of glycol ethers for forward osmotic control.

    PubMed

    Nakayama, Daichi; Mok, Yeongbong; Noh, Minwoo; Park, Jeongseon; Kang, Sunyoung; Lee, Yan

    2014-03-21

    Lower critical solution temperature (LCST) phase transition of glycol ether (GE)-water mixtures induces an abrupt change in osmotic pressure driven by a mild temperature change. The temperature-controlled osmotic change was applied for the forward osmosis (FO) desalination. Among three GEs evaluated, di(ethylene glycol) n-hexyl ether (DEH) was selected as a potential FO draw solute. A DEH-water mixture with a high osmotic pressure could draw fresh water from a high-salt feed solution such as seawater through a semipermeable membrane at around 10 °C. The water-drawn DEH-water mixture was phase-separated into a water-rich phase and a DEH-rich phase at around 30 °C. The water-rich phase with a much reduced osmotic pressure released water into a low-salt solution, and the DEH-rich phase was recovered into the initial DEH-water mixture. The phase separation behaviour, the residual GE concentration in the water-rich phase, the osmotic pressure of the DEH-water mixture, and the osmotic flux between the DEH-water mixture and salt solutions were carefully analysed for FO desalination. The liquid-liquid phase separation of the GE-water mixture driven by the mild temperature change between 10 °C and 30 °C is very attractive for the development of an ideal draw solute for future practical FO desalination.

  4. Hydrogen isotope systematics of phase separation in submarine hydrothermal systems: Experimental calibration and theoretical models

    USGS Publications Warehouse

    Berndt, M.E.; Seal, R.R.; Shanks, Wayne C.; Seyfried, W.E.

    1996-01-01

    Hydrogen isotope fractionation factors were measured for coexisting brines and vapors formed by phase separation of NaCl/H2O fluids at temperatures ranging from 399-450??C and pressures from 277-397 bars. It was found that brines are depleted in D compared to coexisting vapors at all conditions studied. The magnitude of hydrogen isotope fractionation is dependent on the relative amounts of Cl in the two phases and can be empirically correlated to pressure using the following relationship: 1000 ln ??(vap-brine) = 2.54(??0.83) + 2.87(??0.69) x log (??P), where ??(vap-brine) is the fractionation factor and ??P is a pressure term representing distance from the critical curve in the NaCl/H2O system. The effect of phase separation on hydrogen isotope distribution in subseafloor hydrothermal systems depends on a number of factors, including whether phase separation is induced by heating at depth or by decompression of hydrothermal fluids ascending to the seafloor. Phase separation in most subseafloor systems appears to be a simple process driven by heating of seawater to conditions within the two-phase region, followed by segregation and entrainment of brine or vapor into a seawater dominated system. Resulting vent fluids exhibit large ranges in Cl concentration with no measurable effect on ??D. Possible exceptions to this include hydrothermal fluids venting at Axial and 9??N on the East Pacific Rise. High ??D values of low Cl fluids venting at Axial are consistent with phase separation taking place at relatively shallow levels in the oceanic crust while negative ??D values in some low Cl fluids venting at 9??N suggest involvement of a magmatic fluid component or phase separation of D-depleted brines derived during previous hydrothermal activity.

  5. Characterization of fish gelatin-gum arabic complex coacervates as influenced by phase separation temperature.

    PubMed

    Anvari, Mohammad; Pan, Cheol-Ho; Yoon, Won-Byong; Chung, Donghwa

    2015-08-01

    The rheological and structural characteristics of fish gelatin (FG)-gum arabic (GA) complex coacervate phase, separated from an aqueous mixture of 1% FG and 1% GA at pH 3.5, were investigated as influenced by phase separation temperature. Decreasing the phase separation temperature from 40 to 10 °C lead to: (1) the formation of a coacervate phase with a larger volume fraction and higher biopolymer concentrations, which is more viscous, more structural resistant at low shear rates, more shear-thinning at high shear rates, and more condensed in microstructure, (2) a solid-like elastic behavior of the phase separated at 10 °C at a high oscillatory frequency, (3) the increase in gelling and melting temperatures of the coacervate phase (3.7-3.9 °C and 6.2-6.9 °C, respectively), (4) the formation of a more rigid and thermo-stable coacervate gel. The coacervate phase is regarded as a homogeneously networked biopolymer matrix dispersed with water vacuoles and its gel as a weak physical gel reinforced by FG-GA attractive electrostatic interactions.

  6. Anion-directed self-organization of thermotropic liquid crystalline materials containing a guanidinium moiety.

    PubMed

    Kim, Dongwoo; Jon, Sangyong; Lee, Hyung-Kun; Baek, Kangkyun; Oh, Nam-Keun; Zin, Wang-Cheol; Kim, Kimoon

    2005-11-28

    New wedge-shaped thermotropic liquid crystalline materials containing a guanidinium moiety at the apex organize into various supramolecular structures such as hexagonal columnar, rectangular columnar and Pm3n cubic mesophases depending on anions illustrating guest-directed self-organization in mesophases.

  7. Evaluation of the Sensitivity of Two-Phase Flow Model for the Steam Separator Analysis

    SciTech Connect

    Michio Murase; Masao Chaki

    2006-07-01

    Reducing of the pressure losses of steam separator systems of boiling water reactor (BWR) plants is useful to reduce the required pump head and enhance core stability design margin. The need to reduce the pressure losses of steam separator systems is especially important in BWR plants that have high power density cores and natural circulation systems. The core flow rate of a BWR plant with a natural circulation system is affected by the pressure losses of steam separator systems. In BWR plants with high power density cores, the core stability design margin is affected by these pressure losses. Generally, reducing the pressure losses of the steam separator systems leads to increased carry-under and carryover. Reducing the pressure losses while keeping the characteristics of both carry-under and carryover is desired, so many studies have been done. The steam separator of a BWR plant consists of a standpipe section, a swirl vane section and three-barrel sections. Two-phase flow of steam and water enters the steam separator through the standpipe section and reaches the swirl vane section. In the swirl vane section, the two-phase flow is given centrifugal force and is basically separated into steam and water. Therefore investigating the two-phase flow characteristics of the swirl vane section is very important. After the swirl vane section, the two-phase flow enters the barrel sections. Each barrel has a pick-off ring. The water in the barrel section is mainly removed by these pick-off rings because the water mainly flows upward as a liquid film in the barrel section due to the centrifugal force given in the swirl vane section. We researched the effect of using the drag force model of the swirling two-phase flow in analyzing a steam separator and we found that the drag force model greatly affects the results of the analysis. (authors)

  8. Ternary Phase-Separation Investigation of Sol-Gel Derived Silica from Ethyl Silicate 40.

    PubMed

    Wang, Shengnan; Wang, David K; Smart, Simon; da Costa, João C Diniz

    2015-09-28

    A ternary phase-separation investigation of the ethyl silicate 40 (ES40) sol-gel process was conducted using ethanol and water as the solvent and hydrolysing agent, respectively. This oligomeric silica precursor underwent various degrees of phase separation behaviour in solution during the sol-gel reactions as a function of temperature and H2O/Si ratios. The solution composition within the immiscible region of the ES40 phase-separated system shows that the hydrolysis and condensation reactions decreased with decreasing reaction temperature. A mesoporous structure was obtained at low temperature due to weak drying forces from slow solvent evaporation on one hand and formation of unreacted ES40 cages in the other, which reduced network shrinkage and produced larger pores. This was attributed to the concentration of the reactive sites around the phase-separated interface, which enhanced the condensation and crosslinking. Contrary to dense silica structures obtained from sol-gel reactions in the miscible region, higher microporosity was produced via a phase-separated sol-gel system by using high H2O/Si ratios. This tailoring process facilitated further condensation reactions and crosslinking of silica chains, which coupled with stiffening of the network, made it more resistant to compression and densification.

  9. Ternary Phase-Separation Investigation of Sol-Gel Derived Silica from Ethyl Silicate 40

    NASA Astrophysics Data System (ADS)

    Wang, Shengnan; Wang, David K.; Smart, Simon; Diniz da Costa, João C.

    2015-09-01

    A ternary phase-separation investigation of the ethyl silicate 40 (ES40) sol-gel process was conducted using ethanol and water as the solvent and hydrolysing agent, respectively. This oligomeric silica precursor underwent various degrees of phase separation behaviour in solution during the sol-gel reactions as a function of temperature and H2O/Si ratios. The solution composition within the immiscible region of the ES40 phase-separated system shows that the hydrolysis and condensation reactions decreased with decreasing reaction temperature. A mesoporous structure was obtained at low temperature due to weak drying forces from slow solvent evaporation on one hand and formation of unreacted ES40 cages in the other, which reduced network shrinkage and produced larger pores. This was attributed to the concentration of the reactive sites around the phase-separated interface, which enhanced the condensation and crosslinking. Contrary to dense silica structures obtained from sol-gel reactions in the miscible region, higher microporosity was produced via a phase-separated sol-gel system by using high H2O/Si ratios. This tailoring process facilitated further condensation reactions and crosslinking of silica chains, which coupled with stiffening of the network, made it more resistant to compression and densification.

  10. Ternary Phase-Separation Investigation of Sol-Gel Derived Silica from Ethyl Silicate 40

    PubMed Central

    Wang, Shengnan; Wang, David K.; Smart, Simon; Diniz da Costa, João C.

    2015-01-01

    A ternary phase-separation investigation of the ethyl silicate 40 (ES40) sol-gel process was conducted using ethanol and water as the solvent and hydrolysing agent, respectively. This oligomeric silica precursor underwent various degrees of phase separation behaviour in solution during the sol-gel reactions as a function of temperature and H2O/Si ratios. The solution composition within the immiscible region of the ES40 phase-separated system shows that the hydrolysis and condensation reactions decreased with decreasing reaction temperature. A mesoporous structure was obtained at low temperature due to weak drying forces from slow solvent evaporation on one hand and formation of unreacted ES40 cages in the other, which reduced network shrinkage and produced larger pores. This was attributed to the concentration of the reactive sites around the phase-separated interface, which enhanced the condensation and crosslinking. Contrary to dense silica structures obtained from sol-gel reactions in the miscible region, higher microporosity was produced via a phase-separated sol-gel system by using high H2O/Si ratios. This tailoring process facilitated further condensation reactions and crosslinking of silica chains, which coupled with stiffening of the network, made it more resistant to compression and densification. PMID:26411484

  11. Movie of phase separation during physics of colloids in space experiment

    NASA Technical Reports Server (NTRS)

    2002-01-01

    Still photographs taken over 16 hours on Nov. 13, 2001, on the International Space Station have been condensed into a few seconds to show the de-mixing -- or phase separation -- process studied by the Experiment on Physics of Colloids in Space. Commanded from the ground, dozens of similar tests have been conducted since the experiment arrived on ISS in 2000. The sample is a mix of polymethylmethacrylate (PMMA or acrylic) colloids, polystyrene polymers and solvents. The circular area in the video is 2 cm (0.8 in.) in diameter. The phase separation process occurs spontaneously after the sample is mechanically mixed. The evolving lighter regions are rich in colloid and have the structure of a liquid. The dark regions are poor in colloids and have the structure of a gas. This behavior carnot be observed on Earth because gravity causes the particles to fall out of solution faster than the phase separation can occur. While similar to a gas-liquid phase transition, the growth rate observed in this test is different from any atomic gas-liquid or liquid-liquid phase transition ever measured experimentally. Ultimately, the sample separates into colloid-poor and colloid-rich areas, just as oil and vinegar separate. The fundamental science of de-mixing in this colloid-polymer sample is the same found in the annealing of metal alloys and plastic polymer blends. Improving the understanding of this process may lead to improving processing of these materials on Earth.

  12. Phase separation during the Experiment on Physics of Colloids in Space

    NASA Technical Reports Server (NTRS)

    2003-01-01

    Still photographs taken over 16 hours on Nov. 13, 2001, on the International Space Station have been condensed into a few seconds to show the de-mixing -- or phase separation -- process studied by the Experiment on Physics of Colloids in Space. Commanded from the ground, dozens of similar tests have been conducted since the experiment arrived on ISS in 2000. The sample is a mix of polymethylmethacrylate (PMMA or acrylic) colloids, polystyrene polymers and solvents. The circular area is 2 cm (0.8 in.) in diameter. The phase separation process occurs spontaneously after the sample is mechanically mixed. The evolving lighter regions are rich in colloid and have the structure of a liquid. The dark regions are poor in colloids and have the structure of a gas. This behavior carnot be observed on Earth because gravity causes the particles to fall out of solution faster than the phase separation can occur. While similar to a gas-liquid phase transition, the growth rate observed in this test is different from any atomic gas-liquid or liquid-liquid phase transition ever measured experimentally. Ultimately, the sample separates into colloid-poor and colloid-rich areas, just as oil and vinegar separate. The fundamental science of de-mixing in this colloid-polymer sample is the same found in the annealing of metal alloys and plastic polymer blends. Improving the understanding of this process may lead to improving processing of these materials on Earth.

  13. Ferromagnetic and antiferromagnetic orders of a phase-separated manganite probed throughout the B -T phase diagram

    NASA Astrophysics Data System (ADS)

    Windsor, Y. W.; Tanaka, Yoshikazu; Scagnoli, V.; Garganourakis, M.; de Souza, R. A.; Medarde, M.; Cheong, S.-W.; Staub, U.

    2016-12-01

    We employ resonant soft x-ray diffraction (RSXD) to isolate the signal from the CE-type antiferromagnetic phase of (La,Pr)1- xC axMn O3 (with x ≈3 /8 ), and follow only this phase through the known phases of the material in the B -T phase diagram. This material is known to exhibit a range of electronic ordering phenomena, most notably a metal-insulator transition (associated with colossal magnetoresistance) and phase separation between the antiferromagnetic phase and a ferromagnetic phase. Bulk magnetization measurements under the same B -T conditions were also conducted, giving a full picture of both phases for direct side-by-side comparison. The comparison specifically focuses on the metal-insulator transition. Upon magnetic field ramping to this transition, we find that the CE-type order undergoes a sharp quench at high temperatures (above phase coexistence temperatures) but that at lower temperatures, where the CE order is metastable, the transition broadens significantly. At the lowest temperatures, where a spin glass-type phase is expected, a slow annihilation of remanent CE domains is observed. Finally, a refined phase diagram is presented.

  14. Separating pairing from quantum phase coherence dynamics above the superconducting transition by femtosecond spectroscopy

    PubMed Central

    Madan, I.; Kurosawa, T.; Toda, Y.; Oda, M.; Mertelj, T.; Kusar, P.; Mihailovic, D.

    2014-01-01

    In classical superconductors an energy gap and phase coherence appear simultaneously with pairing at the transition to the superconducting state. In high-temperature superconductors, the possibility that pairing and phase coherence are distinct and independent processes has led to intense experimental search of their separate manifestations. Using femtosecond spectroscopy methods we now show that it is possible to clearly separate fluctuation dynamics of the superconducting pairing amplitude from the phase relaxation above the critical transition temperature. Empirically establishing a close correspondence between the superfluid density measured by THz spectroscopy and superconducting optical pump-probe response over a wide region of temperature, we find that in differently doped Bi2Sr2CaCu2O8+δ crystals the pairing gap amplitude monotonically extends well beyond Tc, while the phase coherence shows a pronounced power-law divergence as T → Tc, thus showing that phase coherence and gap formation are distinct processes which occur on different timescales. PMID:25014162

  15. The nature of phase separation in a Ru-Sn-O ternary oxide electrocatalyst.

    PubMed

    Wang, Xin; Deng, Fenyong; Tang, Zhongzhi; Wu, Bo; Tang, Dian; Lin, Wei

    2013-03-21

    A phase stability diagram of ruthenium-zirconium oxide (Ru-Sn-O) was constructed by a combination of ab initio density functional theory and thermodynamic calculations. Results suggest that the phase separation/segregation that has been reported in the literature for the RuO(2)-SnO(2) system is through a typical spinodal decomposition mechanism. Ru(0.45)Sn(0.55)O(2) films were prepared by thermal co-decomposition of precursors at 500 °C for varied duration. Quantitative phase analyses of the prepared films based on X-ray diffraction and high-resolution transmission electron microscopy confirmed the spinodal nature of the phase separation. The present fundamental study provides a theoretical guideline for the phase and microstructure design of Ru-Sn-O based mixed oxides for electrocatalysis applications.

  16. Grafted nanoparticles as soft patchy colloids: Self-assembly versus phase separation

    SciTech Connect

    Mahynski, Nathan A.; Panagiotopoulos, Athanassios Z.

    2015-02-21

    We investigate the thermodynamic behavior of a model polymer-grafted nanoparticle (GNP) system on a fine lattice, using grand canonical Monte Carlo simulations, to compare and contrast the validity of two different models for GNPs: “nanoparticle amphiphiles” versus “patchy particles.” In the former model, continuous self-assembly processes are expected to dominate the system, whereas the latter are characterized by first-order phase separation into novel equilibrium phases such as “empty liquids.” We find that, in general, considering GNPs as amphiphiles within the framework of a recent mean-field theory [Pryamtisyn et al., J. Chem. Phys. 131, 221102 (2009)] provides a qualitatively accurate description of the thermodynamics of GNP systems, revealing either first-order phase separation into two isotropic phases or continuous self-assembly. Our model GNPs display no signs of empty liquid formation, suggesting that these nanoparticles do not provide a route to such phases.

  17. Design and Development of Gas-Liquid Cylindrical Cyclone Compact Separators for Three-Phase Flow

    SciTech Connect

    Mohan, Ram S.; Shoham, Ovadia

    1999-10-28

    The objective of this five-year project (October, 1997--September, 2002) is to expand the current research activities of Tulsa University Separation Technology Projects (TUSTP) to multiphase oil/water/gas separation. This project will be executed in two phases. Phase I (1997--2000) will focus on the investigations of the complex multiphase hydrodynamic flow behavior in a three-phase Gas-Liquid Cylindrical Cyclone (GLCC) Separator. The activities of this phase will include the development of a mechanistic model, a computational fluid dynamics (CFD) simulator, and detailed experimentation on the three-phase GLCC. The experimental and CFD simulation results will be suitably integrated with the mechanistic model. In Phase II (2000--2002), the developed GLCC separator will be tested under high pressure and real crudes conditions. This is crucial for validating the GLCC design for field application and facilitating easy and rapid technology deployment. Design criteria for industrial applications will be developed based on these results and will be incorporated into the mechanistic model by TUSTP.

  18. Design and Development of Gas-Liquid Cylindrical Cyclone Compact Separators for Three-Phase Flow

    SciTech Connect

    Mohan, R.S.; Shoham, O.

    2001-01-18

    The objective of this five-year project (October 1997 - September 2002) was to expand the current research activities of Tulsa University Separation Technology Projects (TUSTP) to multiphase oil/water/gas separation. This project was executed in two phases. Phase I (1997 - 2000) focused on the investigations of the complex multiphase hydrodynamic flow behavior in a three-phase Gas-Liquid Cylindrical Cyclone (GLCC) Separator. The activities of this phase included the development of a mechanistic model, a computational fluid dynamics (CFD) simulator, and detailed experimentation on the three-phase GLCC. The experimental and CFD simulation results will be suitably integrated with the mechanistic model. In Phase II (2000 - 2002), the developed GLCC separator will be tested under high pressure and real crude conditions. This is crucial for validating the GLCC design for field application and facilitating easy and rapid technology deployment. Design criteria for industrial applications will be developed based on these results and will be incorporated into the mechanistic model by TUSTP.

  19. Design and Development of Gas-Liquid Cylindrical Cyclone Compact Separators for Three-Phase Flow

    SciTech Connect

    Mohan, R.S.; Shoham, O.

    2001-01-10

    The objective of this five-year project (October 1997--September 2002) was to expand the current research activities of Tulsa University Separation Technology Projects (TUSTP) to multiphase oil/water/gas separation. This project was executed in two phases. Phase I (1997--2000) focused on the investigations of the complex multiphase hydrodynamic flow behavior in a three-phase Gas-Liquid Cylindrical Cyclone (GLCC) Separator. The activities of this phase included the development of a mechanistic model, a computational fluid dynamics (CFD) simulator, and detailed experimentation on the three-phase GLCC. The experimental and CFD simulation results will be suitably integrated with the mechanistic model. In Phase II (2000--2002), the developed GLCC separator will be tested under high pressure and real crude conditions. This is crucial for validating the GLCC design for field application and facilitating easy and rapid technology deployment. Design criteria for industrial applications will be developed based on these results and will be incorporated into the mechanistic model by TUSTP.

  20. D0 Silicon Upgrade: Calc. to Determine Need for a N2 Phase Separator

    SciTech Connect

    Rucinski, Russ; /Fermilab

    1995-04-07

    A nitrogen phase separator is recommended on the liquid supply line at the helium refrigerator plant. This engineering note documents the calculations done to reach that conclusion. The steady state liquid nitrogen consumption rate for the refrigerator, VLPC and solenoid systems is about 30 gal/hr. The estimated heat leak for the piping run to the refrigerator location is 50 watts. The calculated quality at the refrigerator was 0.032. Given this quality, a two phase flow model based on Lockhart-Martinelli and also incorporating Baker diagram nomenclature was run on TK solver. The result of this program was that without the use of a phase separator we could expect a slug flow pattern with a volume fraction of gas of 65%. Based on this, I recommend that we use a phase separator to siphon off the gas before the nitrogen is sent to a standard saver type subcooler. Including the phase separator will help ensure proper operation of the subcooler. The subcooler will help us attempt to deliver single phase liquid to the nitrogen control valves.

  1. Simultaneous separation of hydrophobic and hydrophilic peptides with a silica hydride stationary phase using aqueous normal phase conditions.

    PubMed

    Boysen, Reinhard I; Yang, Yuanzhong; Chowdhury, Jamil; Matyska, Maria T; Pesek, Joseph J; Hearn, Milton T W

    2011-11-04

    The application of a silica hydride modified stationary phase with low organic loading has been investigated as a new type of chromatographic material suitable for the separation and analysis of peptides with electrospray ionization mass spectrometric detection. Retention maps were established to delineate the chromatographic characteristics of a series of peptides with physical properties ranging from strongly hydrophobic to very hydrophilic and encompassing a broad range of pI values (pI 5.5-9.4). The effects of low concentrations of two additives (formic acid and acetic acid) in the mobile phase were also investigated with respect to their contribution to separation selectivity and retention under comparable conditions. Significantly, strong retention of both the hydrophobic and the hydrophilic peptides was observed when high-organic low-aqueous mobile phases were employed, thus providing a new avenue to achieve high resolution peptide separations. For example, simultaneous separation of hydrophobic and hydrophilic peptides was achieved under aqueous normal phase (ANP) chromatographic conditions with linear gradient elution procedures in a single run, whilst further gradient optimization enabled improved peak efficiencies of the more strongly retained hydrophobic and hydrophilic peptides.

  2. Enantiomeric separations of ruthenium (II) polypyridyl complexes using HPLC with cyclofructan chiral stationary phases.

    PubMed

    Shu, Yang; Breitbach, Zachary S; Dissanayake, Milan K; Perera, Sirantha; Aslan, Joseph M; Alatrash, Nagham; MacDonnell, Frederick M; Armstrong, Daniel W

    2015-01-01

    The enantiomeric separation of 21 ruthenium (II) polypyridyl complexes was achieved with a novel class of cyclofructan-based chiral stationary phases (CSPs) in the polar organic mode. Aromatic derivatives on the chiral selectors proved to be essential for enantioselectivity. The R-napthylethyl carbamate functionalized cyclofructan 6 (LARIHC CF6-RN) column proved to be the most effective overall, while the dimethylphenyl carbamate cyclofructan 7 (LARIHC CF7-DMP) showed complementary selectivity. A combination of acid and base additives was necessary for optimal separations. The retention factor vs. acetonitrile/methanol ratio plot showed a U-shaped retention curve, indicating that different interactions take place at different polar organic solvent compositions. The separation results indicated that π-π interactions, steric effects, and hydrogen bonding contribute to the enantiomeric separation of ruthenium (II) polypyridyl complexes with cyclofructan chiral stationary phases in the polar organic mode.

  3. Viscosity and phase separations of binary CO-He and CO-Ar mixtures

    NASA Astrophysics Data System (ADS)

    Rademacher, N.; Bayarjargal, L.; Morgenroth, W.; Ciezak-Jenkins, J. A.; Winkler, B.

    2015-01-01

    Binary mixtures of 10 and 25 vol% CO in He and 10 vol% CO in Ar have been studied at high pressures and ambient temperature in diamond anvil cells. Phase separations were observed at 5.7(3) GPa, 3.6(2) GPa and 1.6(1) GPa. Earlier studies of ?-He mixtures of comparable concentrations revealed phase separations at significantly larger pressures, while ?-Ar mixtures separate at pressures comparable to those observed in the CO-Ar system here. The viscosity of a CO-rich fluid phase was determined by measuring the velocities of rising He bubbles. After corrections for the influence of the finite container size and of remaining helium in CO, the viscosity of the CO-rich fluid at 3.8(1) GPa was ≈3(1) mPa s, similar to what would be expected for isoelectronic liquid ? under the same conditions.

  4. Phase separation in dilute solutions of 3He in solid 4He

    NASA Astrophysics Data System (ADS)

    Huan, C.; Yin, L.; Xia, J. S.; Candela, D.; Cowan, B. P.; Sullivan, N. S.

    2017-03-01

    We report the results of studies of the phase separation of solid solutions of dilute concentrations of 3He in 4He. The temperatures and the kinetics of the phase separation were determined from NMR experiments for 3He concentrations 1.6 ×10-5phase separation temperatures are found to be in excellent agreement with regular solution theory as augmented by Edwards and Balibar [Phys. Rev. B 39, 4083 (1989), 10.1103/PhysRevB.39.4083]. The growth of 3He droplets shows a t1 /3 time dependence at long times consistent with Ostwald ripening.

  5. Effect of Iron Oxide and Phase Separation on the Color of Blue Jun Ware Glaze.

    PubMed

    Wang, Fen; Yang, Changan; Zhu, Jianfeng; Lin, Ying

    2015-09-01

    Based on the traditional Jun ware glaze, the imitated Jun ware glazes were prepared by adding iron oxide and introducing phase separation agent apatite through four-angle-method. The effect of iron oxide contents, phase separation and the firing temperature on the color of Jun ware glazes were investigated by a neutral atmosphere experiment, optical microscope and scanning electronic microscope. The results showed that the colorant, mainly Fe2O3, contributed to the Jun ware glaze blue and cyan colors of Jun ware glaze. The light scatter caused by the small droplets in phase separation structure only influenced the shade of the glaze color, intensify or weaken the color, and thus made the glaze perfect and elegant opal visual effects, but was not the origin of general blue or cyan colors of Jun ware glaze. In addition, the firing temperature and the basic glaze composition affected the glaze colors to some extent.

  6. Device for two-dimensional gas-phase separation and characterization of ion mixtures

    DOEpatents

    Tang, Keqi; Shvartsburg, Alexandre A.; Smith, Richard D.

    2006-12-12

    The present invention relates to a device for separation and characterization of gas-phase ions. The device incorporates an ion source, a field asymmetric waveform ion mobility spectrometry (FAIMS) analyzer, an ion mobility spectrometry (IMS) drift tube, and an ion detector. In one aspect of the invention, FAIMS operating voltages are electrically floated on top of the IMS drift voltage. In the other aspect, the FAIMS/IMS interface is implemented employing an electrodynamic ion funnel, including in particular an hourglass ion funnel. The present invention improves the efficiency (peak capacity) and sensitivity of gas-phase separations; the online FAIMS/IMS coupling creates a fundamentally novel two-dimensional gas-phase separation technology with high peak capacity, specificity, and exceptional throughput.

  7. Recent progress of chiral stationary phases for separation of enantiomers in gas chromatography.

    PubMed

    Xie, Sheng-Ming; Yuan, Li-Ming

    2017-01-01

    Chromatography techniques based on chiral stationary phases are widely used for the separation of enantiomers. In particular, gas chromatography has developed rapidly in recent years due to its merits such as fast analysis speed, lower consumption of stationary phases and analytes, higher column efficiency, making it a better choice for chiral separation in diverse industries. This article summarizes recent progress of novel chiral stationary phases based on cyclofructan derivatives and chiral porous materials including chiral metal-organic frameworks, chiral porous organic frameworks, chiral inorganic mesoporous materials, and chiral porous organic cages in gas chromatography, covering original research papers published since 2010. The chiral recognition properties and mechanisms of separation toward enantiomers are also introduced.

  8. Theory of spatiotemporally resolved spectroscopy for phase-separation dynamics in electron-hole systems

    NASA Astrophysics Data System (ADS)

    Ishikawa, Akira

    2013-02-01

    Phase separation such as the formation of electron-hole droplets has been observed in semiconductor electron-hole systems. In such conventional experiments, the information averaged in real space was obtained. However, in recent years, optical-near-field techniques have enabled us to acquire spatial information. In this study, I propose a theoretical formulation of spatiotemporal dynamics and spatiotemporally resolved optical response of the gas-liquid phase separation in electron-hole systems. In addition, the nature of the nonequilibrium open system is an essential point in electron-hole systems. Therefore, I investigate the effect of the finite lifetime of electron-hole pairs on phase-separation dynamics. Contribution to the Topical Issue "Excitonic Processes in Condensed Matter, Nanostructured and Molecular Materials", edited by Maria Antonietta Loi, Jasper Knoester and Paul H. M. van Loosdrecht.

  9. Influence of red blood cell clustering on phase separation in capillary networks

    NASA Astrophysics Data System (ADS)

    Podgorski, Thomas; Boucly, Celine; Coupier, Gwennou

    2014-11-01

    We investigate the flow of red blood cell suspensions in microfluidic bifurcations and capillary networks. At strong degrees of confinement, such as those encountered in the microcirculation, phase separation takes place at bifurcations of the network, leading to strong heterogeneities and fluctuations of the hematocrit (blood cell concentration). We highlight the influence of the mechanical properties of cells : an increase of membrane or cytoplasm rigidity, as can happen in pathologies such as sickle cell disease tends to reduce the phase separation. The influence of the attractive interaction between cells, that leads to clustering (rouleau formation) was also investigated by varying the concentration of macromolecules in the solution (dextran or fibrinogen). We show that hydrodynamic stresses in bifurcations can lead to rupture of clusters at a critical speed which increases with interaction energy. Overall, the clustering phenomenon tends to increase phase separation and hematocrit heterogeneities.

  10. Coarse-grained molecular dynamics simulation of binary charged lipid membranes: Phase separation and morphological dynamics

    NASA Astrophysics Data System (ADS)

    Ito, Hiroaki; Higuchi, Yuji; Shimokawa, Naofumi

    2016-10-01

    Biomembranes, which are mainly composed of neutral and charged lipids, exhibit a large variety of functional structures and dynamics. Here, we report a coarse-grained molecular dynamics (MD) simulation of the phase separation and morphological dynamics in charged lipid bilayer vesicles. The screened long-range electrostatic repulsion among charged head groups delays or inhibits the lateral phase separation in charged vesicles compared with neutral vesicles, suggesting the transition of the phase-separation mechanism from spinodal decomposition to nucleation or homogeneous dispersion. Moreover, the electrostatic repulsion causes morphological changes, such as pore formation, and further transformations into disk, string, and bicelle structures, which are spatiotemporally coupled to the lateral segregation of charged lipids. Based on our coarse-grained MD simulation, we propose a plausible mechanism of pore formation at the molecular level. The pore formation in a charged-lipid-rich domain is initiated by the prior disturbance of the local molecular orientation in the domain.

  11. Therapeutic Antibody Engineering To Improve Viscosity and Phase Separation Guided by Crystal Structure.

    PubMed

    Chow, Chi-Kin; Allan, Barrett W; Chai, Qing; Atwell, Shane; Lu, Jirong

    2016-03-07

    Antibodies at high concentrations often reveal unanticipated biophysical properties suboptimal for therapeutic development. The purpose of this work was to explore the use of point mutations based on crystal structure information to improve antibody physical properties such as viscosity and phase separation (LLPS) at high concentrations. An IgG4 monoclonal antibody (Mab4) that exhibited high viscosity and phase separation at high concentration was used as a model system. Guided by the crystal structure, four CDR point mutants were made to evaluate the role of hydrophobic and charge interactions on solution behavior. Surprisingly and unpredictably, two of the charge mutants, R33G and N35E, showed a reduction in viscosity and a lower propensity to form LLPS at high concentration compared to the wild-type (WT), while a third charge mutant S28K showed an increased propensity to form LLPS compared to the WT. A fourth mutant, F102H, had reduced hydrophobicity, but unchanged viscosity and phase separation behavior. We further evaluated the correlation of various biophysical measurements including second virial coefficient (A2), interaction parameter (kD), weight-average molecular weight (WAMW), and hydrodynamic diameters (DH), at relatively low protein concentration (4 to 15 mg/mL) to physical properties, such as viscosity and liquid-liquid phase separation (LLPS), at high concentration. Surprisingly, kD measured using dynamic light scattering (DLS) at low antibody concentration correlated better with viscosity and phase separation than did A2 for Mab4. Our results suggest that the high viscosity and phase separation observed at high concentration for Mab4 are mainly driven by charge and not hydrophobicity.

  12. Anion separations for liquid chromatography using propylpyridinium silica as the stationary phase.

    PubMed

    Auler, Lúcia M L A; Silva, César R; Bottoli, Carla B G; Collins, Carol H

    2011-05-30

    This work describes the characterization and potential applications of a silica-based anion-exchange phase prepared by a two-step modification process that incorporates a propylpyridinium group. The effects of pH and eluent concentration on anion separation were examined using 150 mm × 3.9 mm HPLC columns packed with the new phase. The mobile phase pH values ranged from 3.8 to 6.6 using phthalic acid/Tris solutions. The best separation was achieved using 2.5 mmol L(-1) phthalate/2.4 mmol L(-1) Tris solution at pH 4.2 as mobile phase with non-suppressed conductivity detection. The new stationary phase was used for the separation of some inorganic and organic anions showing good resolution. The stability of the silica-based anion exchange phase was also evaluated. Analytical curves, for concentrations ranging from 0.25 to 10 mg L(-1) for the inorganic anions chloride, nitrite, bromide and nitrate, showed good linear correlations (r>0.998). The method was tested with certified rainwater samples. The measured and certified values were in good agreement, indicating that the new phase holds significant promise for the analysis of these anions in environmental samples.

  13. Exploring the dynamics of phase separation in colloid-polymer mixtures with long range attraction.

    PubMed

    Sabin, Juan; Bailey, Arthur E; Frisken, Barbara J

    2016-06-28

    We have studied the kinetics of phase separation and gel formation in a low-dispersity colloid - non-adsorbing polymer system with long range attraction using small-angle light scattering. This system exhibits two-phase and three-phase coexistence of gas, liquid and crystal phases when the strength of attraction is between 2 and 4kBT and gel phases when the strength of attraction is increased. For those samples that undergo macroscopic phase separation, whether to gas-crystal, gas-liquid or gas-liquid-crystal coexistence, we observe dynamic scaling of the structure factor and growth of a characteristic length scale that behaves as expected for phase separation in fluids. In samples that gel, the power law associated with the growth of the dominant length scale is not equal to 1/3, but appears to depend mainly on the strength of attraction, decreasing from 1/3 for samples near the coexistence region to 1/27 at 8kBT, over a wide range of colloid and polymer concentrations.

  14. How to separate ionic liquids: use of hydrophilic interaction liquid chromatography and mixed mode phases.

    PubMed

    Lamouroux, C; Foglia, G; Le Rouzo, G

    2011-05-20

    This chromatographic study deals with the development of a convenient and versatile method to separate Room Temperature Ionic Liquids. Different modes of chromatography were studied. The study attempts to answer the following question: "what were the most important interactions for the separation of ionic liquids?". The results show that the essential interactions to assure a good retention of RTILs are the ionic ones and that hydrophobic interactions play a role in the selectivity of the separation. The separation of five imidazolium salt with a traditional diol columns in Hydrophilic Interaction Chromatography (HILIC) was demonstrated. It shows that neutral diol grafted column allows an important retention that we assume is due to the capability of diol to develop a thick layer of water. Furthermore, stationary phase based on mixed interaction associating ion exchange and hydrophobic properties were studied. Firstly, it will be argued that it is possible to separate RTILs with a convenient retention and resolution according to a reverse phase elution with the Primesep columns made of a brush type long alkyl chain with an embedded negatively charged functional group. Secondly, a sucessful separation of RTILs in HILIC mode with a mixed phase column containing a cationic exchanger and a hydrophobic octyl chain length will be demonstrated.

  15. Systematic Approach to Links between Separations in MEKC and Reversed-Phase HPLC.

    PubMed

    Ferguson, P D; Goodall, D M; Loran, J S

    1998-10-01

    Retention factors and partition coefficients in micellar electrokinetic chromatography (MEKC) and reversed-phase high-performance liquid chromatography (RP-HPLC) are compared for a series of alkylbenzenes and substituted phenols. In both techniques, separations are based on partitioning between an aqueous phase and an alkyl phase. In MEKC, this was an SDS (C12) micellar pseudostationary phase, and in RP-HPLC an ODS 2 (C18) stationary phase. A nonporous silica (Micra 1.5-μm NPS), which has a low carbon loading, was used rather than a standard porous silica to avoid excessive retention in HPLC and to allow identical mobile phase conditions to be used in both separation modes. The average ratio of analyte retention factors, k(MEKC):k(HPLC), was found to be equal to the ratio β(MEKC):β(HPLC), where β is the phase ratio. This implies that partition coefficients, P, are similar in both MEKC and HPLC, since P = k/β, and that the dominant contribution to stability within each alkyl phase arises from hydrophobic interactions which are common to both separation media. Since partition coefficients are similar in MEKC and HPLC under aqueous buffer conditions, information on retention in one technique may be transferred to the other, provided that the phase ratios are known. In MEKC and HPLC, linear correlations of log octanol-water partition coefficients, K(ow), vs log k for the test compounds were transformed, knowing the phase ratio, to give log P values as a function of log K(ow). This allows quantitative links between MEKC and HPLC to be extended to include octanol-water partitioning. The addition of acetonitrile as an organic modifier over the concentration range 0-20% (v/v) was found to have a greater effect on k in HPLC than in MEKC. This could be a result of a decrease in the MEKC phase ratio due to an increase in the critical micelle concentration.

  16. Controlling phase separation of binary Bose-Einstein condensates via mixed-spin-channel Feshbach resonance

    SciTech Connect

    Tojo, Satoshi; Taguchi, Yoshihisa; Masuyama, Yuta; Hayashi, Taro; Hirano, Takuya; Saito, Hiroki

    2010-09-15

    We investigate controlled phase separation of a binary Bose-Einstein condensate in the proximity of a mixed-spin-channel Feshbach resonance in the |F=1,m{sub F}=+1> and |F=2,m{sub F}=-1> states of {sup 87}Rb at a magnetic field of 9.10 G. Phase separation occurs on the lower-magnetic-field side of the Feshbach resonance while the two components overlap on the higher-magnetic-field side. The Feshbach resonance curve of the scattering length is obtained from the shape of the atomic cloud by comparison with the numerical analysis of coupled Gross-Pitaevskii equations.

  17. Submicron-scale manipulation of phase separation in organic solar cells

    NASA Astrophysics Data System (ADS)

    Chen, Fang-Chung; Lin, Yi-Kai; Ko, Chu-Jung

    2008-01-01

    This paper describes a method for controlling the submicron-scale phase separation of poly(3-hexylthiophene) and (6,6)-phenyl-C61-butyric acid methyl ester in organic solar cells. Using microcontact printing of self-assembled monolayers on the device buffer layer to divide the surface into two regimes having different surface energies, an interdigitated structure aligned vertical to the substrate surface is achieved after spontaneous surface-directed phase separation. The power conversion efficiency increases upon decreasing the grating spacing, reaching 2.47%. The hole mobility increased as a consequence of improved polymer chain ordering, resulting in higher device efficiency, while smaller pattern sizes were used.

  18. Feedback stabilization of the Cahn-Hilliard type system for phase separation

    NASA Astrophysics Data System (ADS)

    Barbu, Viorel; Colli, Pierluigi; Gilardi, Gianni; Marinoschi, Gabriela

    2017-02-01

    This article is concerned with the internal feedback stabilization of the phase field system of Cahn-Hilliard type, modeling the phase separation in a binary mixture. Under suitable assumptions on an arbitrarily fixed stationary solution, we construct via spectral separation arguments a feedback controller having its support in an arbitrary open subset of the space domain, such that the closed loop nonlinear system exponentially reaches the prescribed stationary solution. This feedback controller has a finite dimensional structure in the state space of solutions. In particular, every constant stationary solution is admissible.

  19. Influence of recrystallization on phase separation kinetics of oxide dispersion strengthened Fe Cr Al alloy

    SciTech Connect

    Capdevila, C.; Miller, Michael K; Pimentel, G.; Chao, J.

    2012-01-01

    The effect of different starting microstructures on the kinetics of Fe-rich ({alpha}) and Cr-rich ({alpha}') phase separation during aging of Fe-Cr-Al oxide dispersion strengthened (ODS) alloys has been analyzed with a combination of atom probe tomography and thermoelectric power measurements. The results revealed that the high recrystallization temperature necessary to produce a coarse grained microstructure in Fe-base ODS alloys affects the randomness of Cr-atom distributions and defect density, which consequently affect the phase separation kinetics at low annealing temperatures.

  20. [Separation of enantiomers by supercritical fluid chromatography on polysaccharide derivative-based chiral stationary phases].

    PubMed

    Li, Dongyan; Wu, Xi; Hao, Fangli; Yang, Yang; Chen, Xiaoming

    2016-01-01

    Eleven kinds of chiral compounds have been well separated within 10 min on polysaccharide derivative-based chiral stationary phases named Chiralpak IA, IB, IC, ID, IE and IF by supercritical fluid chromatography (SFC). The chiral recognition of these chiral compounds has demonstrated good complementary enantioselectivities of the six chiral columns, which were proved to be useful for chiral SFC. Both the elution time and enantioselectivies could be significantly affected by the modifier types and their concentrations, such as methanol, ethanol and isopropanol, which should be optimized during the experiments. In addition, the solvent versatility of the immobilized chiral stationary phase on the optimization of the chiral separation was helpful.

  1. An atom probe perspective on phase separation and precipitation in duplex stainless steels

    DOE PAGES

    Garfinkel, David A.; Tucker, Julie D.; Haley, Daniel A.; ...

    2016-05-16

    Here, three-dimensional chemical imaging of Fe–Cr alloys showing Fe-rich (α)/Cr-rich (α') phase separation is reported using atom probe tomography techniques. The extent of phase separation, i.e., amplitude and wavelength, has been quantitatively assessed using the Langer-Bar-on-Miller, proximity histogram, and autocorrelation function methods for two separate Fe–Cr alloys, designated 2101 and 2205. Although the 2101 alloy possesses a larger wavelength and amplitude after annealing at 427 °C for 100–10 000 h, it exhibits a lower hardness than the 2205 alloy. In addition to this phase separation, ultra-fine Ni–Mn–Si–Cu-rich G-phase precipitates form at the α/α' interfaces in both alloys. For the 2101more » alloy, Cu clusters act to form a nucleus, around which a Ni–Mn–Si shell develops during the precipitation process. For the 2205 alloy, the Ni and Cu atoms enrich simultaneously and no core–shell chemical distribution was found. This segregation phenomenon may arise from the exact Ni/Cu ratio inside the ferrite. After annealing for 10 000 h, the number density of the G-phase within the 2205 alloy was found to be roughly one order of magnitude higher than in the 2101 alloy. The G-phase precipitates have an additional deleterious effect on the thermal embrittlement, as evaluated by the Ashby–Orowan equation, which explains the discrepancy between the hardness and the rate of phase separation with respect to annealing time (Gladman T 1999 Mater. Sci. Tech. Ser. 15 30–36).« less

  2. An atom probe perspective on phase separation and precipitation in duplex stainless steels

    SciTech Connect

    Garfinkel, David A.; Tucker, Julie D.; Haley, Daniel A.; Young, George A.; Guo, Wei; Poplawsky, Jonathan D.

    2016-05-16

    Here, three-dimensional chemical imaging of Fe–Cr alloys showing Fe-rich (α)/Cr-rich (α') phase separation is reported using atom probe tomography techniques. The extent of phase separation, i.e., amplitude and wavelength, has been quantitatively assessed using the Langer-Bar-on-Miller, proximity histogram, and autocorrelation function methods for two separate Fe–Cr alloys, designated 2101 and 2205. Although the 2101 alloy possesses a larger wavelength and amplitude after annealing at 427 °C for 100–10 000 h, it exhibits a lower hardness than the 2205 alloy. In addition to this phase separation, ultra-fine Ni–Mn–Si–Cu-rich G-phase precipitates form at the α/α' interfaces in both alloys. For the 2101 alloy, Cu clusters act to form a nucleus, around which a Ni–Mn–Si shell develops during the precipitation process. For the 2205 alloy, the Ni and Cu atoms enrich simultaneously and no core–shell chemical distribution was found. This segregation phenomenon may arise from the exact Ni/Cu ratio inside the ferrite. After annealing for 10 000 h, the number density of the G-phase within the 2205 alloy was found to be roughly one order of magnitude higher than in the 2101 alloy. The G-phase precipitates have an additional deleterious effect on the thermal embrittlement, as evaluated by the Ashby–Orowan equation, which explains the discrepancy between the hardness and the rate of phase separation with respect to annealing time (Gladman T 1999 Mater. Sci. Tech. Ser. 15 30–36).

  3. An atom probe perspective on phase separation and precipitation in duplex stainless steels

    NASA Astrophysics Data System (ADS)

    Guo, Wei; Garfinkel, David A.; Tucker, Julie D.; Haley, Daniel; Young, George A.; Poplawsky, Jonathan D.

    2016-06-01

    Three-dimensional chemical imaging of Fe-Cr alloys showing Fe-rich (α)/Cr-rich (α‧) phase separation is reported using atom probe tomography techniques. The extent of phase separation, i.e., amplitude and wavelength, has been quantitatively assessed using the Langer-Bar-on-Miller, proximity histogram, and autocorrelation function methods for two separate Fe-Cr alloys, designated 2101 and 2205. Although the 2101 alloy possesses a larger wavelength and amplitude after annealing at 427 °C for 100-10 000 h, it exhibits a lower hardness than the 2205 alloy. In addition to this phase separation, ultra-fine Ni-Mn-Si-Cu-rich G-phase precipitates form at the α/α‧ interfaces in both alloys. For the 2101 alloy, Cu clusters act to form a nucleus, around which a Ni-Mn-Si shell develops during the precipitation process. For the 2205 alloy, the Ni and Cu atoms enrich simultaneously and no core-shell chemical distribution was found. This segregation phenomenon may arise from the exact Ni/Cu ratio inside the ferrite. After annealing for 10 000 h, the number density of the G-phase within the 2205 alloy was found to be roughly one order of magnitude higher than in the 2101 alloy. The G-phase precipitates have an additional deleterious effect on the thermal embrittlement, as evaluated by the Ashby-Orowan equation, which explains the discrepancy between the hardness and the rate of phase separation with respect to annealing time (Gladman T 1999 Mater. Sci. Tech. Ser. 15 30-36). ).

  4. Fraction transfer process in on-line comprehensive two-dimensional liquid-phase separations.

    PubMed

    Česla, Petr; Křenková, Jana

    2017-01-01

    Two-dimensional liquid-phase separations have gained increasing attention for their ability to separate complex sample mixtures. Among the experimental setups used, an on-line approach is preferred to reduce the probability of sample contamination, for easier automation and high-sample throughput. The interfacing of the separation techniques in the on-line mode brings additional demands on proper optimization of the two-dimensional system. In this review, the possibilities of the on-line coupling of liquid chromatography and liquid chromatography with capillary electrophoresis in two-dimensional systems are discussed. Special attention is paid to the fraction transfer process, which includes an overview of interfaces and experimental setups applied, the compatibility issues of separation systems, and instrumental parameters. The benefits and drawbacks of using electromigration separations in combination with liquid chromatography are presented as well.

  5. Parametric study on phase separation of binary mixtures in a lid driven cavity: A DPD study

    NASA Astrophysics Data System (ADS)

    Gidituri, Harinadha; Anand, Vijay; Panchagnula, Mahesh; Vedantam, Srikanth

    2016-11-01

    We investigate the phase separation behavior of binary mixtures in two dimensional periodic and lid driven cavity domains using dissipative particle dynamics (DPD). The effect of DPD parameters like repulsion coefficient, dissipative coefficient, cut-off radius, and weight function exponent on domain size growth has been studied. The phase separation is delayed for low values of repulsion coefficient. Under these conditions, a few clusters of the dispersed phase are distributed in a continuous phase. This is because of weak inter-particle repulsion. As we increase the repulsion coefficient value, this behavior disappears. The domain growth rate is also observed to increase with an increase in the value of the dissipation coefficient as well as cut-off radius. Finally, the dynamics of phase separation in the lid driven cavity problem are significantly different when compared to that in the periodic domain, due to the formation of a stable vortex in the cavity. The vortex results in a dynamic equilibrium between clustering and separation. The distribution of cluster sizes is studied as a function of the driven cavity parameters.

  6. Structural Characterization of Phase Separation in Fe-Cr: A Current Comparison of Experimental Methods

    NASA Astrophysics Data System (ADS)

    Xu, Xin; Odqvist, Joakim; Colliander, Magnus Hörnqvist; Thuvander, Mattias; Steuwer, Axel; Westraadt, Johan E.; King, Stephen; Hedström, Peter

    2016-12-01

    Self-assembly due to phase separation within a miscibility gap is important in numerous material systems and applications. A system of particular interest is the binary alloy system Fe-Cr, since it is both a suitable model material and the base system for the stainless steel alloy category, suffering from low-temperature embrittlement due to phase separation. Structural characterization of the minute nano-scale concentration fluctuations during early phase separation has for a long time been considered a major challenge within material characterization. However, recent developments present new opportunities in this field. Here, we present an overview of the current capabilities and limitations of different techniques. A set of Fe-Cr alloys were investigated using small-angle neutron scattering (SANS), atom probe tomography, and analytical transmission electron microscopy. The complementarity of the characterization techniques is clear, and combinatorial studies can provide complete quantitative structure information during phase separation in Fe-Cr alloys. Furthermore, we argue that SANS provides a unique in-situ access to the nanostructure, and that direct comparisons between SANS and phase-field modeling, solving the non-linear Cahn Hilliard equation with proper physical input, should be pursued.

  7. Phase separation kinetics in amorphous solid dispersions upon exposure to water.

    PubMed

    Purohit, Hitesh S; Taylor, Lynne S

    2015-05-04

    The purpose of this study was to develop a novel fluorescence technique employing environment-sensitive fluorescent probes to study phase separation kinetics in hydrated matrices of amorphous solid dispersions (ASDs) following storage at high humidity and during dissolution. The initial miscibility of the ASDs was confirmed using infrared (IR) spectroscopy and differential scanning calorimetry (DSC). Fluorescence spectroscopy, as an independent primary technique, was used together with conventional confirmatory techniques including DSC, X-ray diffraction (XRD), fluorescence microscopy, and IR spectroscopy to study phase separation phenomena. By monitoring the emission characteristics of the environment-sensitive fluorescent probes, it was possible to successfully monitor amorphous-amorphous phase separation (AAPS) as a function of time in probucol-poly(vinylpyrrolidone) (PVP) and ritonavir-PVP ASDs after exposure to water. In contrast, a ritonavir-hydroxypropylmethylcellulose acetate succinate (HPMCAS) ASD, did not show AAPS and was used as a control to demonstrate the capability of the newly developed fluorescence method to differentiate systems that showed no phase separation following exposure to water versus those that did. The results from the fluorescence studies were in good agreement with results obtained using various other complementary techniques. Thus, fluorescence spectroscopy can be utilized as a fast and efficient tool to detect and monitor the kinetics of phase transformations in amorphous solid dispersions during hydration and will help provide mechanistic insight into the stability and dissolution behavior of amorphous solid dispersions.

  8. Phase separation in aqueous solutions of lens gamma-crystallins: special role of gamma s.

    PubMed Central

    Liu, C; Asherie, N; Lomakin, A; Pande, J; Ogun, O; Benedek, G B

    1996-01-01

    We have studied liquid-liquid phase separation in aqueous ternary solutions of calf lens gamma-crystallin proteins. Specifically, we have examined two ternary systems containing gamma s--namely, gamma IVa with gamma s in water and gamma II with gamma s in water. For each system, the phase-separation temperatures (Tph (phi)) alpha as a function of the overall protein volume fraction phi at various fixed compositions alpha (the "cloud-point curves") were measured. For the gamma IVa, gamma s, and water ternary solution, a binodal curve composed of pairs of coexisting points, (phi I, alpha 1) and (phi II, alpha II), at a fixed temperature (20 degrees C) was also determined. We observe that on the cloud-point curve the critical point is at a higher volume fraction than the maximum phase-separation temperature point. We also find that typically the difference in composition between the coexisting phases is at least as significant as the difference in volume fraction. We show that the asymmetric shape of the cloud-point curve is a consequence of this significant composition difference. Our observation that the phase-separation temperature of the mixtures in the high volume fraction region is strongly suppressed suggests that gamma s-crystallin may play an important role in maintaining the transparency of the lens. PMID:8552642

  9. Glucaminium ionic liquid-functionalized stationary phase for the separation of nucleosides in hydrophilic interaction chromatography.

    PubMed

    Jiang, Qiong; Zhang, Mingliang; Wang, Xusheng; Guo, Yong; Qiu, Hongdeng; Zhang, Shusheng

    2015-10-01

    A glucaminium-based ionic liquid stationary phase was prepared via facile epoxy-amine reaction and subsequent quaternization. Successful immobilization of glucaminium-based ionic liquid onto silica surface was validated by elemental analysis and infrared spectroscopy. The new stationary phase was evaluated for the separation of nucleosides in hydrophilic interaction liquid chromatography (HILIC). Effects of various factors, such as acetonitrile concentration, salt concentration, pH value, as well as column temperature, on the chromatographic behavior toward nucleosides were studied in detail. The results indicated that this new stationary phase can be used for separation of water-soluble polar substances in HILIC mode. The retention of solutes on the stationary phase was influenced by a mixed-mode retention mechanism with a combination of adsorptive and partitioning interactions.

  10. Stress reduction in phase-separated, cross-linked networks: influence of phase structure and kinetics of reaction.

    PubMed

    Szczepanski, Caroline R; Stansbury, Jeffrey W

    2014-10-05

    A mechanism for polymerization shrinkage and stress reduction was developed for heterogeneous networks formed via ambient, photo-initiated polymerization-induced phase separation (PIPS). The material system used consists of a bulk homopolymer matrix of triethylene glycol dimethacrylate (TEGDMA) modified with one of three non-reactive, linear prepolymers (poly-methyl, ethyl and butyl methacrylate). At higher prepolymer loading levels (10-20 wt%) an enhanced reduction in both shrinkage and polymerization stress is observed. The onset of gelation in these materials is delayed to a higher degree of methacrylate conversion (~15-25%), providing more time for phase structure evolution by thermodynamically driven monomer diffusion between immiscible phases prior to network macro-gelation. The resulting phase structure was probed by introducing a fluorescently tagged prepolymer into the matrix. The phase structure evolves from a dispersion of prepolymer at low loading levels to a fully co-continuous heterogeneous network at higher loadings. The bulk modulus in phase separated networks is equivalent or greater than that of poly(TEGDMA), despite a reduced polymerization rate and cross-link density in the prepolymer-rich domains.

  11. Stress reduction in phase-separated, cross-linked networks: influence of phase structure and kinetics of reaction

    PubMed Central

    Szczepanski, Caroline R.; Stansbury, Jeffrey W.

    2014-01-01

    A mechanism for polymerization shrinkage and stress reduction was developed for heterogeneous networks formed via ambient, photo-initiated polymerization-induced phase separation (PIPS). The material system used consists of a bulk homopolymer matrix of triethylene glycol dimethacrylate (TEGDMA) modified with one of three non-reactive, linear prepolymers (poly-methyl, ethyl and butyl methacrylate). At higher prepolymer loading levels (10–20 wt%) an enhanced reduction in both shrinkage and polymerization stress is observed. The onset of gelation in these materials is delayed to a higher degree of methacrylate conversion (~15–25%), providing more time for phase structure evolution by thermodynamically driven monomer diffusion between immiscible phases prior to network macro-gelation. The resulting phase structure was probed by introducing a fluorescently tagged prepolymer into the matrix. The phase structure evolves from a dispersion of prepolymer at low loading levels to a fully co-continuous heterogeneous network at higher loadings. The bulk modulus in phase separated networks is equivalent or greater than that of poly(TEGDMA), despite a reduced polymerization rate and cross-link density in the prepolymer-rich domains. PMID:25418999

  12. Analysis of Phase Separation in High Performance PbTe–PbS Thermoelectric Materials

    SciTech Connect

    Girard, Steven N.; Schmidt-Rohr, Klaus; Chasapis, Thomas C.; Hatzikraniotis, Euripides; Njegic, B.; Levin, E. M.; Rawal, A.; Paraskevopoulos, Konstantios M.; Kanatzidis, Mercouri G.

    2013-02-11

    Phase immiscibility in PbTe–based thermoelectric materials is an effective means of top-down synthesis of nanostructured composites exhibiting low lattice thermal conductivities. PbTe1-x Sx thermoelectric materials can be synthesized as metastable solid solution alloys through rapid quenching. Subsequent post-annealing induces phase separation at the nanometer scale, producing nanostructures that increase phonon scattering and reduce lattice thermal conductivity. However, there has yet to be any study investigating in detail the local chemical structure of both the solid solution and nanostructured variants of this material system. Herein, quenched and annealed (i.e., solid solution and phase-separated) samples of PbTe–PbS are analyzed by in situ high-resolution synchrotron powder X-ray diffraction, solid-state 125Te nuclear magnetic resonance (NMR), and infrared (IR) spectroscopy analysis. For high concentrations of PbS in PbTe, e.g., x >16%, NMR and IR analyses reveal that rapidly quenched samples exhibit incipient phase separation that is not detected by state-of-the-art synchrotron X-ray diffraction, providing an example of a PbTe thermoelectric “alloy” that is in fact phase inhomogeneous. Thermally-induced PbS phase separation in PbTe–PbS occurs close to 200 °C for all compositions studied, and the solubility of the PbS phase in PbTe at elevated temperatures >500 °C is reported. The findings of this study suggest that there may be a large number of thermoelectric alloy systems that are phase inhomogeneous or nanostructured despite adherence to Vegard's Law of alloys, highlighting the importance of careful chemical characterization to differentiate between thermoelectric alloys and composites.

  13. Cell separation in immunoaffinity partition in aqueous polymer two-phase systems

    NASA Technical Reports Server (NTRS)

    Karr, Laurel J.; Van Alstine, James M.; Snyder, Robert S.; Shafer, Steven G.; Harris, J. Milton

    1989-01-01

    Two methods for immunoaffinity partitioning are described. One technique involves the covalent coupling of poly (ethylene glycol) (PEG) to immunoglobulin G antibody preparations. In the second method PEG-modified Protein A is used to complex with cells and unmodified antibody. The effects of PEG molecular weight, the degree of modification, and varying phase system composition on antibody activity and its affinity for the upper phase are studied. It is observed that both methods resulted in effective cell separation.

  14. Hydrodynamic effects on phase separation morphologies in evaporating thin films of polymer solutions

    NASA Astrophysics Data System (ADS)

    Zoumpouli, Garyfalia A.; Yiantsios, Stergios G.

    2016-08-01

    We examine effects of hydrodynamics on phase separation morphologies developed during drying of thin films containing a volatile solvent and two dissolved polymers. Cahn-Hilliard and Flory-Huggins theories are used to describe the free energy of the phase separating systems. The thin films, considered as Newtonian fluids, flow in response to Korteweg stresses arising due to concentration non-uniformities that develop during solvent evaporation. Numerical simulations are employed to investigate the effects of a Peclet number, defined in terms of system physical properties, as well as the effects of parameters characterizing the speed of evaporation and preferential wetting of the solutes at the gas interface. For systems exhibiting preferential wetting, diffusion alone is known to favor lamellar configurations for the separated phases in the dried film. However, a mechanism of hydrodynamic instability of a short length scale is revealed, which beyond a threshold Peclet number may deform and break the lamellae. The critical Peclet number tends to decrease as the evaporation rate increases and to increase with the tendency of the polymers to selectively wet the gas interface. As the Peclet number increases, the instability moves closer to the gas interface and induces the formation of a lateral segregation template that guides the subsequent evolution of the phase separation process. On the other hand, for systems with no preferential wetting or any other property asymmetries between the two polymers, diffusion alone favors the formation of laterally separated configurations. In this case, concentration perturbation modes that lead to enhanced Korteweg stresses may be favored for sufficiently large Peclet numbers. For such modes, a second mechanism is revealed, which is similar to the solutocapillary Marangoni instability observed in evaporating solutions when interfacial tension increases with the concentration of the non-volatile component. This mechanism may lead

  15. Nanoscale phase separation and superconductivity in the one-dimensional Hirsch model

    NASA Astrophysics Data System (ADS)

    Anfossi, Alberto; Degli Esposti Boschi, Cristian; Montorsi, Arianna

    2009-06-01

    We investigate numerically at various fillings the ground state of the one-dimensional Hubbard model with correlated hopping x (Hirsch model). It is found that, for a large range of filling values n around half filling, and for repulsive Coulomb interaction u≤uc(x,n) , phase separation at a nanoscale (NPS phase) between two conducting phases at different densities occurs when x≳2/3 . The NPS phase is accompanied by the opening of a spin gap and the system behaves as a Luther-Emery liquid with dominant superconducting correlations. Close to half filling, an anomalous peak emerges in the charge structure factor related to the density of doubly occupied sites, which determines the size of the droplets in the NPS phase. For 1/2≲x≲2/3 a crossover to a homogeneous phase, still superconducting, takes place.

  16. A Preliminary Assessment of Phase Separator Ground-Based and Reduced-Gravity Testing for ALS Systems

    NASA Technical Reports Server (NTRS)

    Hall, Nancy Rabel

    2006-01-01

    A viewgraph presentation of phase separator ground-based and reduced-gravity testing for Advanced Life Support (ALS) systems is shown. The topics include: 1) Multiphase Flow Technology Program; 2) Types of Separators; 3) MOBI Phase Separators; 4) Experiment set-up; and 5) Preliminary comparison/results.

  17. Photopolymerization-induced crystallization and phase separation in poly(ethylene oxide)/triacrylate blends

    SciTech Connect

    Park, Soo Jeoung; Kyu, Thein

    2008-12-28

    The present article describes experimental and theoretical investigations of miscibility and crystallization behavior of blends of poly(ethylene oxide) (PEO) and triacrylate monomer (TA) using differential scanning calorimetry and optical microscopy. The PEO/TA blends manifested a single T{sub g} varying systematically with composition suggestive of a miscible character in their amorphous states. Moreover, there occurs melting point depression of PEO crystals with increasing TA. A phase diagram was subsequently established that exhibited a solid+liquid coexistence region bound by the liquidus and solidus lines, followed by an upper critical solution temperature (UCST) at a lower temperature. The emerging phase morphology was investigated to verify the coexistence regions. Upon photopolymerization in the isotropic melt above the melting point depression curve, both the UCST and the melting temperatures move upward and eventually surpass the reaction temperature, resulting in phase separation as well as crystallization of PEO driven by the changing supercooling, i.e., the thermodynamic driving force. Of particular interest is the interplay between photopolymerization-induced phase separation and crystallization, which eventually determines the final phase morphology of the PEO/TA blend such as crystalline lamellae, sheaf, or spherulites in isotropic liquid, phase separated domains, and viscous fingering liquids.

  18. Photopolymerization-induced crystallization and phase separation in poly(ethylene oxide)/triacrylate blends.

    PubMed

    Park, Soo Jeoung; Kyu, Thein

    2008-12-28

    The present article describes experimental and theoretical investigations of miscibility and crystallization behavior of blends of poly(ethylene oxide) (PEO) and triacrylate monomer (TA) using differential scanning calorimetry and optical microscopy. The PEO/TA blends manifested a single T(g) varying systematically with composition suggestive of a miscible character in their amorphous states. Moreover, there occurs melting point depression of PEO crystals with increasing TA. A phase diagram was subsequently established that exhibited a solid+liquid coexistence region bound by the liquidus and solidus lines, followed by an upper critical solution temperature (UCST) at a lower temperature. The emerging phase morphology was investigated to verify the coexistence regions. Upon photopolymerization in the isotropic melt above the melting point depression curve, both the UCST and the melting temperatures move upward and eventually surpass the reaction temperature, resulting in phase separation as well as crystallization of PEO driven by the changing supercooling, i.e., the thermodynamic driving force. Of particular interest is the interplay between photopolymerization-induced phase separation and crystallization, which eventually determines the final phase morphology of the PEO/TA blend such as crystalline lamellae, sheaf, or spherulites in isotropic liquid, phase separated domains, and viscous fingering liquids.

  19. Selective Separation of Fe-Concentrates in EAF Slags Using Mechanical Dissimilarity of Solid Phases

    NASA Astrophysics Data System (ADS)

    Jung, Sung Suk; Jung, Keeyoung; Sohn, Il

    2017-02-01

    We sought to develop an optimized particle size-dependent separation method to lower the Fe content of pulverized glass-ceramic electric arc furnace (EAF) slag for its improved reclamation as construction materials by considering the structures and the mechanical behavior of the discrete solid phases. After an isothermal crystallization process to enhance the spinel growth, the Vickers hardness and fracture toughness were measured on the spinel and amorphous phases separately from the solidified slag using indentation methods. The characteristic differences in the hardness of the phases were magnified when this glass-ceramic composite was isothermally crystallized. The hardness of the spinel was observed to be lower in slags with higher FetO/Al2O3 mass ratios due to the triclinic unit cell expansion of the spinel, whereas the hardness of the amorphous phase decreased with increasing isothermal period because of the structural transformation into a silicate-dominant network. Fracture toughness could be calculated based on the hardness and crack length, where the Young's modulus was determined using nanoindentation. The amorphous phase with a lower Fe content and lower fracture toughness resulted in finer powder distribution after pulverization, allowing better separation of the primary crystalline spinel containing higher Fe content from the Fe-deficient amorphous phase according to the particle size.

  20. Investigation of high velocity separator for particle removal in coal gasification plants. Phase II report

    SciTech Connect

    Linhardt, H.D.

    1980-01-15

    This report summarizes the results of Phase II of the High Velocity Particle Separator Program performed under Contract EF-77-C-01-2709. This high velocity wedge separator has the potential to reduce equipment size and cost of high temperature and pressurized particulate removal equipment for coal derived gases. Phase II has been directed toward testing and detailed conceptual design of an element suitable for a commercial scale high temperature, high pressure particle separator (HTPS). Concurrently, Phase IA has been conducted, which utilized the ambient analog method (AAM) for aerodynamic and collection performance investigation of each HTPS configuration prior and during hot testing. This report summarizes the results of Phase IA and II. The AAM effort established correlation of theoretical analysis and experiment for HTPS pressure drop, purge flow ratio and collection efficiency potential. Task I defined the initial test conditions to be the contract design point of 1800/sup 0/F and 350 psia. The 1800/sup 0/F, 350 psia testing represents the main high temperature testing with coal-derived particulates in the 2 to 10 micron range. Phase IA and Phase II have demonstrated efficient particle collection with acceptable pressure drop. In view of these encouraging results, it is reasonable to apply the developed technology toward future hot gas particulate cleanup requirements.

  1. Liquid-liquid phase separation in supersaturated lysozyme solutions and associated precipitate formation/crystallization

    NASA Astrophysics Data System (ADS)

    Muschol, Martin; Rosenberger, Franz

    1997-08-01

    Using cloud point determinations, the phase boundaries (binodals) for metastable liquid-liquid (L-L) separation in supersaturated hen egg white lysozyme solutions with 3%, 5%, and 7% (w/v) NaCl at pH=4.5 and protein concentrations c between 40 and 400 mg/ml were determined. The critical temperature for the binodal increased approximately linearly with salt concentration. The coexisting liquid phases both remained supersaturated but differed widely in protein concentration. No salt repartitioning was observed between the initial and the two separated liquid phases. After the L-L separation, due to the presence of the high protein concentration phase, crystallization occurred much more rapidly than in the initial solution. At high initial protein concentrations, a metastable gel phase formed at temperatures above the liquid binodal. Both crystal nucleation and gel formation were accelerated in samples that had been cycled through the binodal. Solutions in the gel and L-L regions yielded various types of precipitates. Based on theoretical considerations, previous observations with other proteins, and our experimental results with lysozyme, a generic phase diagram for globular proteins is put forth. A limited region in the (T,c) plane favorable for the growth of protein single crystals is delineated.

  2. Liquid-Liquid Phase Separation in Supersaturated Lysozyme Solutions and Associated Precipitate Formation/Crystallization

    NASA Technical Reports Server (NTRS)

    Muschol, Martin; Rosenberger, Franz

    1997-01-01

    Using cloud point determinations, the phase boundaries (binodals) for metastable liquid-liquid (L-L) separation in supersaturated hen egg white lysozyme solutions with 3%, 5%, and 7% (wlv) NaCl at pH= 4.5 and protein concentrations c between 40 and 400 mg/ml were determined. The critical temperature for the binodal increased approximately linearly with salt concentration. The coexisting liquid phases both remained supersaturated but differed widely in protein concentration. No salt repartitioning was observed between the initial and the two separated liquid phases. After the L-L separation, due to the presence of the high protein concentration phase, crystallization occurred much more rapidly than in the initial solution. At high initial protein concentrations, a metastable gel phase formed at temperatures above the liquid binodal. Both crystal nucleation and gel formation were accelerated in samples that had been cycled through the binodal. Solutions in the gel and L-L regions yielded various types of precipitates. Based on theoretical considerations, previous observations with other proteins, and our experimental results with lysozyme, a generic phase diagram for globular proteins is put forth. A limited region in the (T,c) plane favorable for the growth of protein single crystals is delineated.

  3. Influence of thermal effects on the morphological patterns developed through phase separation in binary systems

    NASA Astrophysics Data System (ADS)

    Borzacchiello, D.; Leygue, A.; Chinesta, F.

    2014-07-01

    This paper is concerned with the modelling and numerical simulation of temperature-induced phase separation (TIPS) coupled with non-uniform temperature fields. The spontaneous phase separation of an initially homogeneous blend can be used, in principle, as a reliable and scalable process to reproduce specific morphologies at the microscopic scale in two-phase composite materials, such as rubber-reinforced resins, or in microstructured porous media. The size of the microstructures that are formed and the degree of anisotropy can be controlled through the imposition of an adequate temperature field. In order to understand the potential use of a temperature gradient to control phase separation, we developed a qualitative model for TIPS based on the Cahn-Hilliard approach and we proposed a computational strategy to obtain numerical solutions for phase separation in confined domains taking into account the thermal interaction with the walls. While the method is based on a volume penalization technique, the novelty of the proposed approach relies on the fact that the penalization term of the equation is constructed on the same theoretical basis from which the Cahn-Hilliard equation is derived. The advantage offered by this technique is that the same pseudo-spectral Fourier discretization schemes that are classically used to solve the Cahn-Hilliard equation in periodic domains can be straightforwardly applied to the case of bounded domains. The application examples shown in this paper emphasize the key role of the dimensionless number given by the ratio of the characteristic heat propagation time and the characteristic time of the phase separation, and demonstrate how control of the microstructure anisotropy could be achieved through TIPS.

  4. Cesium vacancy ordering in phase-separated CsxFe2-ySe2

    DOE PAGES

    Taddei, Keith M.; Sturza, M.; Chung, Duck -Yung; ...

    2015-09-14

    By simultaneously displaying magnetism and superconductivity in a single phase, the iron-based superconductors provide a model system for the study of magnetism's role in superconductivity. The class of intercalated iron selenide superconductors is unique among these in having the additional property of phase separation and coexistence of two distinct phases—one majority phase with iron vacancy ordering and strong antiferromagnetism, and the other a poorly understood minority microscopic phase with a contested structure. Adding to the intrigue, the majority phase has never been found to show superconductivity on its own while the minority phase has never been successfully synthesized separate frommore » the majority phase. In order to better understand this minority phase, a series of high-quality CsxFe2–ySe2 single crystals with (0.8 ≤ x ≤ 1;0 ≤ y ≤ 0.3) were grown and studied. Neutron and x-ray powder diffraction performed on ground crystals show that the average I4/mmm structure of the minority phase is distinctly different from the high-temperature I4/mmm parent structure. Moreover, single-crystal diffraction reveals the presence of discrete superlattice reflections that remove the degeneracy of the Cs sites in both the majority and minority phases and reduce their structural symmetries from body centered to primitive. Group theoretical analysis in conjunction with structural modeling shows that the observed superlattice reflections originate from three-dimensional Cs vacancy ordering. This model predicts a 25% vacancy of the Cs site in the minority phase which is consistent with the site's refined occupancy. Magnetization measurements performed in tandem with neutron single-crystal diffraction provide evidence that the minority phase is the host of superconductivity. Lastly, our results also reveal a superconducting dome in which the superconducting transition temperature varies as a function of the nominal valence of iron.« less

  5. Influence of Specific Anions on the Orientational Ordering of Thermotropic Liquid Crystals at Aqueous Interfaces

    PubMed Central

    Carlton, Rebecca J.; Ma, C. Derek; Gupta, Jugal K.; Abbott, Nicholas L.

    2012-01-01

    We report that specific anions (of sodium salts) added to aqueous phases at molar concentrations can trigger rapid, orientational ordering transitions in water-immiscible, thermotropic liquid crystals (LCs; e.g., nematic phase of 4′-pentyl-4-cyanobiphenyl, 5CB) contacting the aqueous phases. Anions classified as chaotropic, specifically iodide, perchlorate and thiocyanate, cause 5CB to undergo continuous, concentration-dependent transitions from planar to homeotropic (perpendicular) orientations at LC-aqueous interfaces within 20 s of addition of the anions. In contrast, anions classified as relatively more kosmotropic in nature (fluoride, sulfate, phosphate, acetate, chloride, nitrate, bromide, and chlorate) do not perturb the LC orientation from that observed without added salts (i.e., planar orientation). Surface pressure-area isotherms of Langmuir films of 5CB supported on aqueous salt solutions reveal ion-specific effects ranking in a manner similar to the LC ordering transitions. Specifically, chaotropic salts stabilized monolayers of 5CB to higher surface pressures and areal densities (12.6 mN/m at 27 Å2/molec. for NaClO4) and thus smaller molecular tilt angles (30° from the surface normal for NaClO4) than kosmotropic salts (5.0 mN/m at 38 Å2/molec. with a corresponding tilt angle of 53° for NaCl). These results and others reported herein suggest that anion-specific interactions with 5CB monolayers lead to bulk LC ordering transitions. Support for the proposition that these ion-specific interactions involve the nitrile group was obtained by using a second LC with nitrile groups (E7; ion-specific effects similar to 5CB were observed) and a third LC with fluorine-substituted aromatic groups (TL205; weak dipole and no ion-specific effects were measured). Finally, we also establish that anion-induced orientational transitions in micrometer-thick LC films involve a change in the easy axis of the LC. Overall, these results provide new insights into ionic

  6. Development of optimized mobile phases for protein separation by high performance thin layer chromatography.

    PubMed

    Biller, Julia; Morschheuser, Lena; Riedner, Maria; Rohn, Sascha

    2015-10-09

    In recent years, protein chemistry tends inexorably toward the analysis of more complex proteins, proteoforms, and posttranslational protein modifications. Although mass spectrometry developed quite fast correspondingly, sample preparation and separation of these analytes is still a major issue and quite challenging. For many years, electrophoresis seemed to be the method of choice; nonetheless its variance is limited to parameters such as size and charge. When taking a look at traditional (thin-layer) chromatography, further parameters such as polarity and different mobile and stationary phases can be utilized. Further, possibilities of detection are manifold compared to electrophoresis. Similarly, two-dimensional separation can be also performed with thin-layer chromatography (TLC). As the revival of TLC developed enormously in the last decade, it seems to be also an alternative to use high performance thin-layer chromatography (HPTLC) for the separation of proteins. The aim of this study was to establish an HPTLC separation system that allows a separation of protein mixtures over a broad polarity range, or if necessary allowing to modify the separation with only few steps to improve the separation for a specific scope. Several layers and solvent systems have been evaluated to reach a fully utilized and optimized separation system.

  7. Characterization of the thermotropic behavior and lateral organization of lipid-peptide mixtures by a combined experimental and theoretical approach: effects of hydrophobic mismatch and role of flanking residues.

    PubMed Central

    Morein, Sven; Killian, J Antoinette; Sperotto, Maria Maddalena

    2002-01-01

    A combined experimental and theoretical study was performed on a series of mixtures of dipalmitoylphosphatidylcholine (DPPC) and synthetic peptides to investigate their thermotropic behavior and lateral organization. The experimental study was based on differential scanning calorimetry (DSC) and phosphorous nuclear magnetic resonance ((31)P-NMR) techniques; the theoretical study was based on calculations on a microscopic molecular interaction model, where the lipid-peptide interaction is built on the hydrophobic matching principle. The chosen peptides, WALP and KALP, consist of a hydrophobic stretch, of variable length, of alternating leucine and alanine residues, flanked on both ends with tryptophan and lysine residues, respectively. By systematically varying the peptide hydrophobic length it was thus possible to explore different matching conditions between the peptide's hydrophobic length and the lipid bilayer hydrophobic thickness, and to investigate the potential role of flanking residues. The results show that both the WALP and the KALP peptides tend to favor the liquid-crystalline (or fluid) phase of the system; i.e., they tend to depress the main-transition temperature, T(m), of pure DPPC. However, the detailed effects of both peptides on the lateral phase behavior of the lipid-peptide system are dependent on the peptide length and the type of flanking residues. The results suggest that below T(m), the shortest among the WALP and KALP peptides induce gel-fluid phase separation in the system within an extensive temperature-composition region. The longer the hydrophobic length of the peptides is, the more narrow this region appears to become. PMID:11867456

  8. Separating the strengthening phase in nickel-cobalt alloys doped with tantalum

    NASA Astrophysics Data System (ADS)

    Shaipov, R. Kh.; Kerimov, E. Yu.; Slyusarenko, E. M.

    2017-02-01

    The hardness values of monophasic (fcc solid solution) and biphasic (fcc solid solution and separated phase) nickel-cobalt alloys doped with tantalum are determined using the Vickers method. Based on the resulting data, a composition-structure-hardness diagram is devised for the Co-Ni-Ta system.

  9. A Classroom Demonstration of Water-Induced Phase Separation of Alcohol-Gasoline Biofuel Blends

    ERIC Educational Resources Information Center

    Mueller, Sherry A.; Anderson, James E.; Wallington, Timothy J.

    2009-01-01

    A significant issue associated with ethanol-gasoline blends is the phase separation that occurs with the addition of small volumes of water, producing an ethanol-deficient gasoline layer and an ethanol-rich aqueous layer. The gasoline layer may have a lower-than-desired octane rating due to the decrease in ethanol content, resulting in engine…

  10. Correlating structure with fluorescence emission in phase-separated conjugated-polymer blends.

    PubMed

    Chappell, John; Lidzey, David G; Jukes, Paul C; Higgins, Anthony M; Thompson, Richard L; O'Connor, Stephen; Grizzi, Ilaria; Fletcher, Robert; O'Brien, Jim; Geoghegan, Mark; Jones, Richard A L

    2003-09-01

    Blends of conjugated polymers are frequently used as the active semiconducting layer in light-emitting diodes and photovoltaic devices. Here we report the use of scanning near-field optical microscopy, scanning force microscopy and nuclear-reaction analysis to study the structure of a thin film of a phase-separated blend of two conjugated polymers prepared by spin-casting. We show that in addition to the well-known micrometre-scale phase-separated morphology of the blend, one of the polymers preferentially wets the surface and forms a 10-nm-thick, partially crystallized wetting layer. Using near-field microscopy we identify unexpected changes in the fluorescence emission from the blend that occurs in a 300-nm-wide band located at the interface between the different phase-separated domains. Our measurements provide an insight into the complex structure of phase-separated conjugated-polymer thin films. Characterizing and controlling the properties of the interfaces in such films will be critical in the further development of efficient optoelectronic devices.

  11. Anisotropic imprint of amorphization and phase separation in manganite thin films via laser interference irradiation.

    PubMed

    Ding, Junfeng; Lin, Zhipeng; Wu, Jianchun; Dong, Zhili; Wu, Tom

    2015-02-04

    Materials with mesoscopic structural and electronic phase separation, either inherent from synthesis or created via external means, are known to exhibit functionalities absent in the homogeneous counterparts. One of the most notable examples is the colossal magnetoresistance discovered in mixed-valence manganites, where the coexistence of nano- to micrometer-sized phase-separated domains dictates the magnetotransport. However, it remains challenging to pattern and process such materials into predesigned structures and devices. In this work, a direct laser interference irradiation (LII) method is employed to produce periodic stripes in thin films of a prototypical phase-separated manganite Pr0.65 (Ca0.75 Sr0.25 )0.35 MnO3 (PCSMO). LII induces selective structural amorphization within the crystalline PCSMO matrix, forming arrays with dimensions commensurate with the laser wavelength. Furthermore, because the length scale of LII modification is compatible to that of phase separation in PCSMO, three orders of magnitude of increase in magnetoresistance and significant in-plane transport anisotropy are observed in treated PCSMO thin films. Our results show that LII is a rapid, cost-effective and contamination-free technique to tailor and improve the physical properties of manganite thin films, and it is promising to be generalized to other functional materials.

  12. Configurable lipid membrane gradients quantify diffusion, phase separations and binding densities.

    PubMed

    Liu, Katherine N; Hung, Chen-Min S; Swift, Michael A; Muñoz, Kristen A; Cortez, Jose L; Sanii, Babak

    2015-11-14

    Single-experiment analysis of phospholipid compositional gradients reveals diffusion coefficients, phase separation parameters, and binding densities as a function of localized lipid mixture. Compositional gradients are formed by directed self assembly where rapid-prototyping techniques (i.e., additive manufacturing or laser-cutting) prescribe lipid geometries that self-spread, heal and mix by diffusion.

  13. Realization of a universal and phase-covariant quantum cloning machine in separate cavities

    SciTech Connect

    Fang Baolong; Song Qingming; Ye Liu

    2011-04-15

    We present a scheme to realize a special quantum cloning machine in separate cavities. The quantum cloning machine can copy the quantum information from a photon pulse to two distant atoms. Choosing the different parameters, the method can perform optimal symmetric (asymmetric) universal quantum cloning and optimal symmetric (asymmetric) phase-covariant cloning.

  14. Switchable water: microfluidic investigation of liquid-liquid phase separation mediated by carbon dioxide.

    PubMed

    Lestari, Gabriella; Abolhasani, Milad; Bennett, Darla; Chase, Preston; Günther, Axel; Kumacheva, Eugenia

    2014-08-27

    Increase in the ionic strength of water that is mediated by the reaction of carbon dioxide (CO2) with nitrogenous bases is a promising approach toward phase separation in mixtures of water with organic solvents and potentially water purification. Conventional macroscale studies of this complicated process are challenging, due to its occurrence via several consecutive and concurrent steps, mass transfer limitation, and lack of control over gas-liquid interfaces. We report a new microfluidic strategy for fundamental studies of liquid-liquid phase separation mediated by CO2 as well as screening of the efficiency of nitrogenous agents. A single set of microfluidic experiments provided qualitative and quantitative information on the kinetics and completeness of water-tetrahydrofuran phase separation, the minimum amount of CO2 required to complete phase separation, the total CO2 uptake, and the rate of CO2 consumption by the liquid mixture. The efficiency of tertiary diamines with different lengths of alkyl chain was examined in a time- and labor-efficient manner and characterized with the proposed efficiency parameter. A wealth of information obtained using the MF methodology can facilitate the development of new additives for switchable solvents in green chemistry applications.

  15. Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics.

    PubMed

    Boeynaems, Steven; Bogaert, Elke; Kovacs, Denes; Konijnenberg, Albert; Timmerman, Evy; Volkov, Alex; Guharoy, Mainak; De Decker, Mathias; Jaspers, Tom; Ryan, Veronica H; Janke, Abigail M; Baatsen, Pieter; Vercruysse, Thomas; Kolaitis, Regina-Maria; Daelemans, Dirk; Taylor, J Paul; Kedersha, Nancy; Anderson, Paul; Impens, Francis; Sobott, Frank; Schymkowitz, Joost; Rousseau, Frederic; Fawzi, Nicolas L; Robberecht, Wim; Van Damme, Philip; Tompa, Peter; Van Den Bosch, Ludo

    2017-03-16

    Liquid-liquid phase separation (LLPS) of RNA-binding proteins plays an important role in the formation of multiple membrane-less organelles involved in RNA metabolism, including stress granules. Defects in stress granule homeostasis constitute a cornerstone of ALS/FTLD pathogenesis. Polar residues (tyrosine and glutamine) have been previously demonstrated to be critical for phase separation of ALS-linked stress granule proteins. We now identify an active role for arginine-rich domains in these phase separations. Moreover, arginine-rich dipeptide repeats (DPRs) derived from C9orf72 hexanucleotide repeat expansions similarly undergo LLPS and induce phase separation of a large set of proteins involved in RNA and stress granule metabolism. Expression of arginine-rich DPRs in cells induced spontaneous stress granule assembly that required both eIF2α phosphorylation and G3BP. Together with recent reports showing that DPRs affect nucleocytoplasmic transport, our results point to an important role for arginine-rich DPRs in the pathogenesis of C9orf72 ALS/FTLD.

  16. Characterization of thermotropism in primary roots of maize: dependence on temperature and temperature gradient, and interaction with gravitropism

    NASA Technical Reports Server (NTRS)

    Poff, K. L.

    1991-01-01

    Thermotropism in primary roots of Zea mays L. was studied with respect to gradient strength (degrees C cm-1), temperature of exposure within a gradient, pre-treatment temperature, and gravitropic stimulation. The magnitude of the response decreased with gradient strength. Maximum thermotropism was independent of gradient strength and pre-treatment temperature. The range of temperature for positive and negative thermotropism did not change with pre-treatment temperature. However, the exact range of temperatures for positive and negative thermotropism varied with gradient strengths. In general, temperatures of exposure lower than 25 degrees C resulted in positive tropic responses while temperatures of exposure of 39 degrees C or more resulted in negative tropic responses. Thermotropism was shown to modify and reverse the normal gravitropic curvature of a horizontal root when thermal gradients were applied opposite the 1 g vector. It is concluded that root thermotropism is a consequence of thermal sensing and that the curvature of the primary root results from the interaction of the thermal and gravitational sensing systems.

  17. Effective protein separation by coupling hydrophobic interaction and reverse phase chromatography for top-down proteomics.

    PubMed

    Xiu, Lichen; Valeja, Santosh G; Alpert, Andrew J; Jin, Song; Ge, Ying

    2014-08-05

    One of the challenges in proteomics is the proteome's complexity, which necessitates the fractionation of proteins prior to the mass spectrometry (MS) analysis. Despite recent advances in top-down proteomics, separation of intact proteins remains challenging. Hydrophobic interaction chromatography (HIC) appears to be a promising method that provides high-resolution separation of intact proteins, but unfortunately the salts conventionally used for HIC are incompatible with MS. In this study, we have identified ammonium tartrate as a MS-compatible salt for HIC with comparable separation performance as the conventionally used ammonium sulfate. Furthermore, we found that the selectivity obtained with ammonium tartrate in the HIC mobile phases is orthogonal to that of reverse phase chromatography (RPC). By coupling HIC and RPC as a novel two-dimensional chromatographic method, we have achieved effective high-resolution intact protein separation as demonstrated with standard protein mixtures and a complex cell lysate. Subsequently, the separated intact proteins were identified by high-resolution top-down MS. For the first time, these results have shown the high potential of HIC as a high-resolution protein separation method for top-down proteomics.

  18. Chromatographic separation of phenylpropanol enantiomers on a quinidine carbamate-type chiral stationary phase

    SciTech Connect

    Asnin, Leonid; Guiochon, Georges A

    2005-07-01

    The retention and the separation of the enantiomers of 1-phenylpropanol (1PP), 2-phenylpropanol (2PP), and 3-chloro-1-phenylpropanol (3CPP) on silica-bonded quinidine carbamate under normal phase HPLC conditions were investigated. A relatively high selectivity of the stationary phase for 3CPP and 1PP ({alpha} {approx} 1.07-1.09) was achieved with eluents containing ethyl acetate as the polar modifier. These mobile phases were examined in detail. Based on the set of chromatographic and thermodynamic data collected, conclusions regarding the mechanism of enantioselectivity and the structure of the selector chiral center are made.

  19. Separation optimization in reversed-phase liquid chromatography by using alkanol additives in the mobile phase: application to amino acids.

    PubMed

    Pappa-Louisi, A; Agrafiotou, P; Georgiadis, I

    2011-09-30

    In an effort to enhance complex mixture separations by using small amounts of a homologous series of alkanols as additives in the mobile phases, it was proposed an optimization algorithm based on a sixth-parameter retention model. This model considers simultaneously the contents of the main organic modifier and of the alkanol additive in the mobile phase as well as of the number of alkyl chain of the additive. This model is in fact a modification of a previously one derived in a recently published paper for the retention description of a mixture of purely hydrophobic alkylbenzenes under isocratic conditions with mobile phases containing alkanol additives. The effectiveness of the new retention model as well as the optimization algorithm was successfully applied to the separation of ten o-phthalaldehyde (OPA) derivatives of amino acids. Indeed, the new retention model exhibited an excellent prediction performance since the obtained overall predictive error between calculated and experimental times was only 2.8% for all isocratic runs by using a variety of mobile phase compositions containing any alkanol homologue even different than those used in the starting/fitting experiments. Moreover, a perfect resolution of the above amino acid mixture was achieved within only 7.4 min in the chromatogram recorded using the optimal mobile phase determined by means of the simple optimization algorithm proposed in this study.

  20. [Separation of bases, phenols and pharmaceuticals on ionic liquid-modified silica stationary phase with pure water as mobile phase].

    PubMed

    Wang, Xusheng; Qiu, Hongdeng; Liu, Xia; Jiang, Shengxiang

    2011-03-01

    N-methylimidazolium ionic liquid (IL) -modified silica was prepared with the reaction of 3-chloropropyl modified silica and N-methylimidazole using toluene as solvent. Based on the multiple interactions between N-methylimidazolium IL-modified silica and analytes such as hydrophobic interaction, electrostatic attraction, repulsion interaction, hydrogen-bonding, etc., the bases (cytosine, thymine, 2-aminopyrimidine and 6-chloroguanine), phenols (m-aminophenol, resorcinol and m-nitrophenol) and three pharmaceuticals (moroxydine hydrochloride, acyclovir and cephalexin hydrate) were separated successfully with only pure water as the mobile phase. These chromatographic separations are environmental friendly, economical and convenient, without any organic solvent or buffer additive. The retention mechanism of these samples on the stationary phase was also investigated.

  1. Steric Pressure among Membrane-Bound Polymers Opposes Lipid Phase Separation.

    PubMed

    Imam, Zachary I; Kenyon, Laura E; Carrillo, Adelita; Espinoza, Isai; Nagib, Fatema; Stachowiak, Jeanne C

    2016-04-19

    Lipid rafts are thought to be key organizers of membrane-protein complexes in cells. Many proteins that interact with rafts have bulky polymeric components such as intrinsically disordered protein domains and polysaccharide chains. Therefore, understanding the interaction between membrane domains and membrane-bound polymers provides insights into the roles rafts play in cells. Multiple studies have demonstrated that high concentrations of membrane-bound polymeric domains create significant lateral steric pressure at membrane surfaces. Furthermore, our recent work has shown that lateral steric pressure at membrane surfaces opposes the assembly of membrane domains. Building on these findings, here we report that membrane-bound polymers are potent suppressors of membrane phase separation, which can destabilize lipid domains with substantially greater efficiency than globular domains such as membrane-bound proteins. Specifically, we created giant vesicles with a ternary lipid composition, which separated into coexisting liquid ordered and disordered phases. Lipids with saturated tails and poly(ethylene glycol) (PEG) chains conjugated to their head groups were included at increasing molar concentrations. When these lipids were sparse on the membrane surface they partitioned to the liquid ordered phase. However, as they became more concentrated, the fraction of GUVs that were phase-separated decreased dramatically, ultimately yielding a population of homogeneous membrane vesicles. Experiments and physical modeling using compositions of increasing PEG molecular weight and lipid miscibility phase transition temperature demonstrate that longer polymers are the most efficient suppressors of membrane phase separation when the energetic barrier to lipid mixing is low. In contrast, as the miscibility transition temperature increases, longer polymers are more readily driven out of domains by the increased steric pressure. Therefore, the concentration of shorter polymers required

  2. Direct observation of mesoscopic phase separation in KxFeySe2 by scanning microwave microscopy

    NASA Astrophysics Data System (ADS)

    Maeda, Atsutaka; Takahashi, Hideyuki; Imai, Yoshinori

    2015-03-01

    KxFeySe2 is isostructural to 122-FeAs compounds. However, its electronic structure is unique among Fe-based superconductors in the sense that hole Fermi pocket is absent at the center of the Brillouin zone. Therefore, it is important to study this compounds in terms of the mechanism of superconductivity since some pairing (for example, s +/- -wave) needs the interaction between hole and electron Fermi pockets. However, the phase separation in this material makes studies using conventional macroscopic measurement techniques very difficult. Scanning near-field microwave microscope (SMM), which can measure local electric property of inhomogeneous conducting samples, should be a powerful tool. Recently we developed the combined instrument of STM and SMM with high sensitivity, and investigated the local electric property of KxFeySe2 (x = 0.8, y = 1.6 ~2, Tc = 31 K) using this scanning tunneling/microwave microscope. The characteristic pattern of mesoscopic phase separation of the metallic and the semiconducting phase was observed. From the comparison with previously reported SEM/EDS result we identified the metallic phase and the semiconducting phase as the minor Fe-rich phase and the major K2Fe4Se5 phase, respectively.

  3. Formation of Asymmetrical Structured Silica Controlled by a Phase Separation Process and Implication for Biosilicification

    PubMed Central

    Shi, Jia-Yuan; Yao, Qi-Zhi; Li, Xi-Ming; Zhou, Gen-Tao; Fu, Sheng-Quan

    2013-01-01

    Biogenetic silica displays intricate patterns assembling from nano- to microsize level and interesting non-spherical structures differentiating in specific directions. Several model systems have been proposed to explain the formation of biosilica nanostructures. Of them, phase separation based on the physicochemical properties of organic amines was considered to be responsible for the pattern formation of biosilica. In this paper, using tetraethyl orthosilicate (TEOS, Si(OCH2CH3)4) as silica precursor, phospholipid (PL) and dodecylamine (DA) were introduced to initiate phase separation of organic components and influence silica precipitation. Morphology, structure and composition of the mineralized products were characterized using a range of techniques including field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), X-ray diffraction (XRD), thermogravimetric and differential thermal analysis (TG-DTA), infrared spectra (IR), and nitrogen physisorption. The results demonstrate that the phase separation process of the organic components leads to the formation of asymmetrically non-spherical silica structures, and the aspect ratios of the asymmetrical structures can be well controlled by varying the concentration of PL and DA. On the basis of the time-dependent experiments, a tentative mechanism is also proposed to illustrate the asymmetrical morphogenesis. Therefore, our results imply that in addition to explaining the hierarchical porous nanopatterning of biosilica, the phase separation process may also be responsible for the growth differentiation of siliceous structures in specific directions. Because organic amine (e.g., long-chair polyamines), phospholipids (e.g., silicalemma) and the phase separation process are associated with the biosilicification of diatoms, our results may provide a new insight into the mechanism of biosilicification. PMID:23585878

  4. Formation of asymmetrical structured silica controlled by a phase separation process and implication for biosilicification.

    PubMed

    Shi, Jia-Yuan; Yao, Qi-Zhi; Li, Xi-Ming; Zhou, Gen-Tao; Fu, Sheng-Quan

    2013-01-01

    Biogenetic silica displays intricate patterns assembling from nano- to microsize level and interesting non-spherical structures differentiating in specific directions. Several model systems have been proposed to explain the formation of biosilica nanostructures. Of them, phase separation based on the physicochemical properties of organic amines was considered to be responsible for the pattern formation of biosilica. In this paper, using tetraethyl orthosilicate (TEOS, Si(OCH2CH3)4) as silica precursor, phospholipid (PL) and dodecylamine (DA) were introduced to initiate phase separation of organic components and influence silica precipitation. Morphology, structure and composition of the mineralized products were characterized using a range of techniques including field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), X-ray diffraction (XRD), thermogravimetric and differential thermal analysis (TG-DTA), infrared spectra (IR), and nitrogen physisorption. The results demonstrate that the phase separation process of the organic components leads to the formation of asymmetrically non-spherical silica structures, and the aspect ratios of the asymmetrical structures can be well controlled by varying the concentration of PL and DA. On the basis of the time-dependent experiments, a tentative mechanism is also proposed to illustrate the asymmetrical morphogenesis. Therefore, our results imply that in addition to explaining the hierarchical porous nanopatterning of biosilica, the phase separation process may also be responsible for the growth differentiation of siliceous structures in specific directions. Because organic amine (e.g., long-chair polyamines), phospholipids (e.g., silicalemma) and the phase separation process are associated with the biosilicification of diatoms, our results may provide a new insight into the mechanism of biosilicification.

  5. Asymmetrical phase separation and gelation in binary mixtures of oppositely charged colloids

    NASA Astrophysics Data System (ADS)

    Zong, Yiwu; Yuan, Guangcui; Han, Charles C.

    2016-07-01

    Two types of colloidal particles, which are nearly the same in chemical composition but carry opposite surface charges, are mixed in water. Depending on the relative proportion of the oppositely charged particles, the process of aggregation leads to the formation of discrete clusters of various sizes in dilute dispersions, and to the development of particle gel networks in more concentrated systems. Due to the significant difference in the absolute values of surface charges (negative particle: -48 mV, positive particle: +24 mV), the phase separation and the gelation behaviors are asymmetric with respect to the mixing ratio. Mixtures with excess negative particles are more stable, while mixtures with excess positive particles are easily affected by phase separation. The hetero-aggregation triggered by the addition of microscopically large macro-ions is similar to what is often observed in a mono-component charged colloidal system, i.e., phase separation occurs through addition of small electrolyte ions. Within the concentration region investigated here, it is clear that the gel line is buried inside the phase separation region. Gelation occurs only when the number and size of the clusters are large and big enough to connect up into a space-spanning network. Our results indicate that, in this binary mixture of oppositely charged colloids, although the interaction between unlike species is attractive and that between like species is repulsive, the onset of gelation is in fact governed by the equilibrium phase separation, as in the case of purely attractive systems with short-range isotropic interaction.

  6. Asymmetrical phase separation and gelation in binary mixtures of oppositely charged colloids.

    PubMed

    Zong, Yiwu; Yuan, Guangcui; Han, Charles C

    2016-07-07

    Two types of colloidal particles, which are nearly the same in chemical composition but carry opposite surface charges, are mixed in water. Depending on the relative proportion of the oppositely charged particles, the process of aggregation leads to the formation of discrete clusters of various sizes in dilute dispersions, and to the development of particle gel networks in more concentrated systems. Due to the significant difference in the absolute values of surface charges (negative particle: -48 mV, positive particle: +24 mV), the phase separation and the gelation behaviors are asymmetric with respect to the mixing ratio. Mixtures with excess negative particles are more stable, while mixtures with excess positive particles are easily affected by phase separation. The hetero-aggregation triggered by the addition of microscopically large macro-ions is similar to what is often observed in a mono-component charged colloidal system, i.e., phase separation occurs through addition of small electrolyte ions. Within the concentration region investigated here, it is clear that the gel line is buried inside the phase separation region. Gelation occurs only when the number and size of the clusters are large and big enough to connect up into a space-spanning network. Our results indicate that, in this binary mixture of oppositely charged colloids, although the interaction between unlike species is attractive and that between like species is repulsive, the onset of gelation is in fact governed by the equilibrium phase separation, as in the case of purely attractive systems with short-range isotropic interaction.

  7. Phase separation of polymer mixtures induced by light and heat: a comparative study by light scattering

    NASA Astrophysics Data System (ADS)

    Ochi, Yuki; Kawakubo, Rie; Van-Pham, Dan-Thuy; Kitamura, Yuki; Nakanishi, Hideyuki; Norisuye, Tomohisa; Tran-Cong-Miyata, Qui

    2015-12-01

    Phase separation of binary blends composed of a polystyrene derivative (PS) and poly (vinyl methyl ether) (PVME) with a lower critical solution temperature (LCST) was experimentally induced by two different methods: heating and UV light irradiation. Using laser light scattering combined with the temperature jump (T-jump) technique, it was demonstrated that in the case of heating, the mixture undergoes phase separation via the nucleation-and-growth (NG) and the spinodal decomposition (SN) processes under shallow and deep quenches, respectively. Particularly, the crossover from the spinodal decomposition to the nucleation-and-growth process was observed at long time under a deep T-jump by light-scattering experiments. On the other hand, in the photo-crosslink case, the PS/PVME blends undergo a nucleation-and-growth process upon irradiation with weak light intensity, whereas the mixture exhibits the spinodal decomposition under irradiation with strong light intensity. From the analysis of the light-scattering data obtained for the blends under the photo-crosslink, the kinetic data reveal the suppression of morphologies having large characteristic length scales. This feature clearly differs from the phase separation induced by heating where no mode-suppression process was observed. It was also found that distribution of the characteristic length scales (the regularity) of the morphology becomes narrow as the phase separation proceeds for reacting blends, whereas it becomes broader as the phase separation proceeds by heating, revealing the important roles of reaction in the suppression of fluctuations with long wavelengths. These experimental results establish a method to control the length scales and the regularity of the morphology of polymer blends by chemical reaction.

  8. Phase separation behavior of egg yolk suspensions after anionic polysaccharides addition.

    PubMed

    Navidghasemizad, Sahar; Temelli, Feral; Wu, Jianping

    2015-03-06

    The objectives of this study were to understand the interactions between three anionic polysaccharides (gum arabic, xanthan gum and ι-carrageenan) and egg yolk at pH 3, 5, 6, 8, 10 and possible phase separation behavior. Zeta potential of egg yolk was not affected by gum arabic addition while it became more negative at pH 5 after xanthan gum and ι-carrageenan addition. The particle size of ι-carrageenan yolk suspension was considerably higher than the other polysaccharide yolk suspensions at pH below 6 but was dramatically decreased at alkaline pH. Most polysaccharide yolk suspensions formed either a biphasic or a monophasic system, whereas three distinct phases were observed for xanthan gum yolk suspension at pH 6. Protein profile analysis of the lipid-rich cream phase obtained from xanthan gum added yolk showed similarities to apoproteins from low density lipoproteins (LDL) of egg yolk. Microscopy analysis indicated the co-presence of xanthan gum and LDL in the creamy phase, within a network formed by xanthan gum. It was suggested that electrostatic and hydrophobic interactions between the egg yolk and xanthan gum as well as xanthan gum's rheological properties could be responsible for the unique phase separation observed in the study. The findings of this study can form the basis for future studies to develop a new method to separate LDL from egg yolk.

  9. Extraordinary phase separation and segregation in vent fluids from the southern East Pacific Rise

    USGS Publications Warehouse

    Von Damm, Karen L.; Lilley, M.D.; Shanks, Wayne C.; Brockington, M.; Bray, A.M.; O'Grady, K. M.; Olson, E.; Graham, A.; Proskurowski, G.

    2003-01-01

    The discovery of Brandon vent on the southern East Pacific Rise is providing new insights into the controls on midocean ridge hydrothermal vent fluid chemistry. The physical conditions at the time ofsampling (287 bar and 405??C) place the Brandon fluids very close to the critical point of seawater (298 bar and 407??C). This permits in situ study of the effects of near criticalphenomena, which are interpreted to be the primary cause of enhanced transition metal transport in these fluids. Of the five orifices on Brandon sampled, three were venting fluids with less than seawater chlorinity, and two were venting fluids with greater than seawater chlorinity. The liquid phase orifices contain 1.6-1.9 times the chloride content of the vapors. Most other elements, excluding the gases, have this same ratio demonstrating the conservative nature of phase separation and the lack of subsequent water-rock interaction. The vapor and liquid phases vent at the same time from orifices within meters of each other on the Brandon structure. Variations in fluid compositions occur on a time scale of minutes. Our interpretation is that phase separation and segregation must be occurring 'real time' within the sulfide structure itself. Fluids from Brandon therefore provide an unique opportunity to understand in situ phase separation without the overprinting of continued water-rock interaction with the oceanic crust, as well as critical phenomena. ?? 2002 Elsevier Science B.V. All rights reserved.

  10. Separation of selected stable isotopes by liquid-phase thermal diffusion and by chemical exchange

    NASA Astrophysics Data System (ADS)

    Rutherford, W. M.; Jepson, B. E.; Michaels, E. D.

    Useful applications of enriched stable nuclides are unduly restricted by high cost and limited availability. Recent research on liquid phase thermal diffusion (LTD) has resulted in practical processes for separating S34, CL35, and CL37 in significant quantities (100 to 500 g/yr) at costs much lower than those associated with the electromagnetic (Calutron) process. The separation of the isotopes of bromine by LTD is now in progress and BR79 is being produced in relatively simple equivalent at a rate on the order of 0.5 g/day. The results of recent measurements show that the isotopes of Zn can be separated by LTD of zinc alkyls. The isotopes of calcium can be separated by LTD and by chemical exchange. The LTD process is based on the use of aqueous Ca(NO3)2 as a working fluid.

  11. Reversed-phase liquid chromatographic separation and simultaneous profiling of steroidal glycoalkaloids and their aglycones.

    PubMed

    Kuronen, P; Väänänen, T; Pehu, E

    1999-11-19

    Improved and simplified reversed-phase liquid chromatographic conditions for the separation and simultaneous profiling of both steroidal glycoalkaloids and their aglycones, having solanidane- or spirosolane-type structures, are described. The most reproducible retention behavior for these ionizable compounds on C18 columns was achieved under isocratic and gradient elution conditions using acetonitrile in combination with triethylammonium phosphate buffer at pH 3.0, when basic functional groups of solutes and silanol groups on the silica are fully protonated minimizing ionic interactions. Gradient elution was the only feasible approach for the simultaneous separation of steroidal glycoalkaloids and their aglycones. A Zorbax SB C18 column, specially designed for low-pH separations, showed good performance in critical separations. The impurities of the commercial tomatine and tomatidine standards were studied and confirmed using mass spectrometric, liquid chromatographic and thin-layer chromatographic methods.

  12. Manipulating electronic phase separation in strongly correlated oxides with an ordered array of antidots

    SciTech Connect

    Zhang, Kai; Du, Kai; Liu, Hao; Zhang, X. -G.; Lan, Fanli; Lin, Hanxuan; Wei, Wengang; Zhu, Yinyan; Kou, Yunfang; Shao, Jian; Niu, Jiebin; Wang, Wenbin; Wu, Ruqian; Yin, Lifeng; Plummer, E. W.; Shen, Jian

    2015-07-20

    The interesting transport and magnetic properties in manganites depend sensitively on the nucleation and growth of electronic phase-separated domains. In this paper, by fabricating antidot arrays in La0.325Pr0.3Ca0.375MnO3 (LPCMO) epitaxial thin films, we create ordered arrays of micrometer-sized ferromagnetic metallic (FMM) rings in the LPCMO films that lead to dramatically increased metal–insulator transition temperatures and reduced resistances. The FMM rings emerge from the edges of the antidots where the lattice symmetry is broken. Based on our Monte Carlo simulation, these FMM rings assist the nucleation and growth of FMM phase domains increasing the metal–insulator transition with decreasing temperature or increasing magnetic field. Finally, this study points to a way in which electronic phase separation in manganites can be artificially controlled without changing chemical composition or applying external field.

  13. Comment on "Phase separation in a two-species Bose mixture"

    NASA Astrophysics Data System (ADS)

    Zhan, Fei; McCulloch, Ian P.

    2014-05-01

    In an article in 2007, Mishra et al. [Phys. Rev. A 76, 013604 (2007), 10.1103/PhysRevA.76.013604] investigated the two-component Bose-Hubbard model using the numerical density-matrix renormalization-group procedure. In the regime of interspecies repulsion Uab larger than the intraspecies repulsion U, they found a transition from a uniform miscible phase to phase separation occurring at a finite value of U, e.g., at around U =1.3 for Δ =Uab/U =1.05 and ρa=ρb=1/2. In this Comment, we show that this result is not correct, and in fact, the two-component Bose-Hubbard model is unstable to phase separation for any Uab>U >0.

  14. Supercooling transition in phase separated manganite thin films: An electrical transport study

    SciTech Connect

    Singh, Sandeep; Kumar, Pawan; Siwach, P. K.; Singh, H. K.; Tyagi, Pawan Kumar

    2014-05-26

    The impact of variation in the relative fractions of the ferromagnetic metallic and antiferromagnetic/charge ordered insulator phases on the supercooling/superheating transition in strongly phase separated system, La{sub 5/8−y}Pr{sub y}Ca{sub 3/8}MnO{sub 3} (y ≈ 0.4), has been studied employing magnetotransport measurements. Our study clearly shows that the supercooling transition temperature is non-unique and strongly depends on the magneto-thermodynamic path through which the low temperature state is accessed. In contrast, the superheating transition temperature remains constant. The thermo-magnetic hysteresis, the separation of the two transitions and the associated resistivity, all are functions of the relative fraction of the coexisting phases.

  15. Manipulating electronic phase separation in strongly correlated oxides with an ordered array of antidots

    PubMed Central

    Zhang, Kai; Du, Kai; Liu, Hao; Zhang, X.-G.; Lan, Fanli; Lin, Hanxuan; Wei, Wengang; Zhu, Yinyan; Kou, Yunfang; Shao, Jian; Niu, Jiebin; Wang, Wenbin; Wu, Ruqian; Yin, Lifeng; Plummer, E. W.; Shen, Jian

    2015-01-01

    The interesting transport and magnetic properties in manganites depend sensitively on the nucleation and growth of electronic phase-separated domains. By fabricating antidot arrays in La0.325Pr0.3Ca0.375MnO3 (LPCMO) epitaxial thin films, we create ordered arrays of micrometer-sized ferromagnetic metallic (FMM) rings in the LPCMO films that lead to dramatically increased metal–insulator transition temperatures and reduced resistances. The FMM rings emerge from the edges of the antidots where the lattice symmetry is broken. Based on our Monte Carlo simulation, these FMM rings assist the nucleation and growth of FMM phase domains increasing the metal–insulator transition with decreasing temperature or increasing magnetic field. This study points to a way in which electronic phase separation in manganites can be artificially controlled without changing chemical composition or applying external field. PMID:26195791

  16. Chemical ordering suppresses large-scale electronic phase separation in doped manganites

    NASA Astrophysics Data System (ADS)

    Zhu, Yinyan; Du, Kai; Niu, Jiebin; Lin, Lingfang; Wei, Wengang; Liu, Hao; Lin, Hanxuan; Zhang, Kai; Yang, Tieying; Kou, Yunfang; Shao, Jian; Gao, Xingyu; Xu, Xiaoshan; Wu, Xiaoshan; Dong, Shuai; Yin, Lifeng; Shen, Jian

    2016-04-01

    For strongly correlated oxides, it has been a long-standing issue regarding the role of the chemical ordering of the dopants on the physical properties. Here, using unit cell by unit cell superlattice growth technique, we determine the role of chemical ordering of the Pr dopant in a colossal magnetoresistant (La1-yPry)1-xCaxMnO3 (LPCMO) system, which has been well known for its large length-scale electronic phase separation phenomena. Our experimental results show that the chemical ordering of Pr leads to marked reduction of the length scale of electronic phase separations. Moreover, compared with the conventional Pr-disordered LPCMO system, the Pr-ordered LPCMO system has a metal-insulator transition that is ~100 K higher because the ferromagnetic metallic phase is more dominant at all temperatures below the Curie temperature.

  17. Vacancy-mediated fcc/bcc phase separation in Fe1-xNix ultrathin films

    DOE PAGES

    Mentes, T. O.; Stojic, N.; Vescovo, E.; ...

    2016-08-01

    The phase separation occurring in Fe-Ni thin lms near the Invar composition is studied by using high resolution spectromicroscopy techniques and density functional theory calculations. Annealed at temperatures around 300 C, Fe0.70Ni0.30 lms on W(110) break into micron-sized bcc and fcc domains with compositions in agreement with the bulk Fe-Ni phase diagram. Ni is found to be the di using species in forming the chemical heterogeneity. The experimentally-determined energy barrier of 1.59 0.09 eV is identi ed as the vacancy formation energy via density functional theory calculations. Thus, the principal role of the surface in the phase separation process ismore » attributed to vacancy creation without interstitials.« less

  18. Manipulating electronic phase separation in strongly correlated oxides with an ordered array of antidots

    DOE PAGES

    Zhang, Kai; Du, Kai; Liu, Hao; ...

    2015-07-20

    The interesting transport and magnetic properties in manganites depend sensitively on the nucleation and growth of electronic phase-separated domains. In this paper, by fabricating antidot arrays in La0.325Pr0.3Ca0.375MnO3 (LPCMO) epitaxial thin films, we create ordered arrays of micrometer-sized ferromagnetic metallic (FMM) rings in the LPCMO films that lead to dramatically increased metal–insulator transition temperatures and reduced resistances. The FMM rings emerge from the edges of the antidots where the lattice symmetry is broken. Based on our Monte Carlo simulation, these FMM rings assist the nucleation and growth of FMM phase domains increasing the metal–insulator transition with decreasing temperature or increasingmore » magnetic field. Finally, this study points to a way in which electronic phase separation in manganites can be artificially controlled without changing chemical composition or applying external field.« less

  19. Separation of nuclei representing different phases of the growth cycle from unsynchronized mammalian cell cultures.

    PubMed

    McBride, O W; Peterson, E A

    1970-10-01

    Nuclei have been isolated from unsynchronized cultures of Chinese hamster fibroblasts after varying intervals of growth following the incorporation of thymidine (-3)H for 20 min. These nuclei were fractionated by unit gravity sedimentation in a stabilizing density gradient of sucrose, and fractions were analyzed for the concentration of nuclei, DNA, and radioactivity. A more rapidly sedimenting population of nuclei in the G(2) phase of the cell cycle was separated from a group of nuclei in the G(1) phase, and nuclei in progressive stages of DNA synthesis (S phase) were distributed between these two regions. The fractionation of intact cells by sedimentation according to their position in the cell cycle was found to be less satisfactory than the corresponding separation of nuclei. This probably results from the continuous accumulation of mass within individual cells throughout the entire cell cycle, whereas most of the mass of a nucleus is replicated during a relatively narrow interval of the total cell cycle.

  20. Long-term stability of phase-separated half-Heusler compounds.

    PubMed

    Krez, J; Balke, B; Ouardi, S; Selle, S; Höche, T; Felser, C; Hermes, W; Schwind, M

    2015-11-28

    Half-Heusler (HH) compounds have shown high figure of merit up to 1.5. Here, we address the long-term stability of n- and p-type HH materials. For this purpose, we investigated HH materials based on the Ti0.3Zr0.35Hf0.35NiSn-system after 500 cycles (1700 h) from 373 to 873 K. Both compounds exhibit a maximum Seebeck coefficient of |α|≈ 210 μV K(-1) and a phase separation into two HH phases. The dendritic microstructure is temperature resistant and upon cycling the changes in the microstructure are so marginal that the low thermal conductivity values (κ < 4 W m(-1) K(-1)) could be maintained. Our results emphasize that phase-separated HH compounds are suitable low cost materials and can lead to enhanced thermoelectric efficiencies beyond the set benchmark for industrial applications.

  1. Modeling the phase separation in binary lipid membrane under externally imposed oscillatory shear flow.

    PubMed

    Chen, Xiao-Bo; Niu, Li-Sha; Shi, Hui-Ji

    2008-09-01

    By adding external velocity terms, the two-dimensional time-dependent Ginzburg-Landau (TDGL) equations are modified. Based on this, the phase separation in binary lipid membrane under externally imposed oscillatory shear flow is numerically modeled employing the Cell Dynamical System (CDS) approach. Considering shear flows with different frequencies and amplitudes, several aspects of such a phase evolving process are studied. Firstly, visualized results are shown via snapshot figures of the membrane shape. And then, the simulated scattering patterns at typical moments are presented. Furthermore, in order to more quantitatively discuss this phase-separation process, the time growth laws of the characteristic domain sizes in both directions parallel and perpendicular to the flow are investigated for each case. Finally, the peculiar rheological properties of such binary lipid membrane system have been discussed, mainly the normal stress difference and the viscoelastic complex shear moduli.

  2. Vacancy-mediated fcc/bcc phase separation in Fe1 -xNix ultrathin films

    NASA Astrophysics Data System (ADS)

    Menteş, T. O.; Stojić, N.; Vescovo, E.; Ablett, J. M.; Niño, M. A.; Locatelli, A.

    2016-08-01

    The phase separation occurring in Fe-Ni thin films near the Invar composition is studied by using high-resolution spectromicroscopy techniques and density functional theory calculations. Annealed at temperatures around 300 ∘C ,Fe0.70Ni0.30 films on W(110) break into micron-sized bcc and fcc domains with compositions in agreement with the bulk Fe-Ni phase diagram. Ni is found to be the diffusing species in forming the chemical heterogeneity. The experimentally determined energy barrier of 1.59 ±0.09 eV is identified as the vacancy formation energy via density functional theory calculations. Thus, the principal role of the surface in the phase separation process is attributed to vacancy creation without interstitials.

  3. Chemical ordering suppresses large-scale electronic phase separation in doped manganites

    PubMed Central

    Zhu, Yinyan; Du, Kai; Niu, Jiebin; Lin, Lingfang; Wei, Wengang; Liu, Hao; Lin, Hanxuan; Zhang, Kai; Yang, Tieying; Kou, Yunfang; Shao, Jian; Gao, Xingyu; Xu, Xiaoshan; Wu, Xiaoshan; Dong, Shuai; Yin, Lifeng; Shen, Jian

    2016-01-01

    For strongly correlated oxides, it has been a long-standing issue regarding the role of the chemical ordering of the dopants on the physical properties. Here, using unit cell by unit cell superlattice growth technique, we determine the role of chemical ordering of the Pr dopant in a colossal magnetoresistant (La1−yPry)1−xCaxMnO3 (LPCMO) system, which has been well known for its large length-scale electronic phase separation phenomena. Our experimental results show that the chemical ordering of Pr leads to marked reduction of the length scale of electronic phase separations. Moreover, compared with the conventional Pr-disordered LPCMO system, the Pr-ordered LPCMO system has a metal–insulator transition that is ∼100 K higher because the ferromagnetic metallic phase is more dominant at all temperatures below the Curie temperature. PMID:27053071

  4. An improved stochastic separated flow model for turbulent two-phase flow

    NASA Astrophysics Data System (ADS)

    Chan, C. K.; Zhang, H. Q.; Lau, K. S.

    An improved stochastic separated flow model is proposed to obtain reasonable statistical characteristics of a two-phase flow. Effects of the history of a particle and its current trajectory position on the mean-square fluctuating velocity of the dispersed phase are continuously considered in this model. Comparing with the conventional model, results using the improved model are more reasonable and can also be obtained more easily. Furthermore, the improved model requires less computational particles for simulating dispersed-phase turbulence at the beginning of the stochastic trajectory. In this paper, an application in turbulent two-phase flow of planar mixing layer is carried out. Numerical results including velocity, mean-square fluctuating velocity, particle number density and pdf of fluctuation velocity of dispersed phase are shown to compare well with experimental data.

  5. Real-Time Volumetric Phase Monitoring: Advancing Chemical Analysis by Countercurrent Separation.

    PubMed

    Pauli, Guido F; Pro, Samuel M; Chadwick, Lucas R; Burdick, Thomas; Pro, Luke; Friedl, Warren; Novak, Nick; Maltby, John; Qiu, Feng; Friesen, J Brent

    2015-07-21

    Countercurrent separation (CCS) utilizes the differential partitioning behavior of analytes between two immiscible liquid phases. We introduce the first platform ("CherryOne") capable of real-time monitoring, metering, and control of the dynamic liquid-liquid CCS process. Automated phase monitoring and volumetrics are made possible with an array of sensors, including the new permittivity-based phase metering apparatus (PMA). Volumetric data for each liquid phase are converted into a dynamic real-time display of stationary phase retention (Sf) and eluent partition coefficients (K), which represent critical parameters of CCS reproducibility. When coupled with the elution-extrusion operational mode (EECCC), automated Sf and K determination empowers untargeted and targeted applications ranging from metabolomic analysis to preparative purifications.

  6. Hygroscopic and phase separation properties of ammonium sulfate/organics/water ternary solutions

    NASA Astrophysics Data System (ADS)

    Zawadowicz, M. A.; Proud, S. R.; Seppalainen, S. S.; Cziczo, D. J.

    2015-08-01

    Atmospheric aerosol particles are often partially or completely composed of inorganic salts, such as ammonium sulfate and sodium chloride, and therefore exhibit hygroscopic properties. Many inorganic salts have well-defined deliquescence and efflorescence points at which they take up and lose water, respectively. Field measurements have shown that atmospheric aerosols are not typically pure inorganic salt, instead, they often also contain organic species. There is ample evidence from laboratory studies that suggests that mixed particles exist in a phase-separated state, with an aqueous inorganic core and organic shell. Although phase separation has not been measured in situ, there is no reason it would not also take place in the atmosphere. Here, we investigate the deliquescence and efflorescence points, phase separation and ability to exchange gas-phase components of mixed organic and inorganic aerosol using a flow tube coupled with FTIR (Fourier transform infrared) spectroscopy. Ammonium sulfate aerosol mixed with organic polyols with different O : C ratios, including 1,4-butanediol, glycerol, 1,2,6-hexanetriol, 1,2-hexanediol, and 1,5-pentanediol have been investigated. Those constituents correspond to materials found in the atmosphere in great abundance and, therefore, particles prepared in this study should mimic atmospheric mixed-phase aerosol particles. Some results of this study tend to be in agreement with previous microscopy experiments, but others, such as phase separation properties of 1,2,6-hexanetriol, do not agree with previous work. Because the particles studied in this experiment are of a smaller size than those used in microscopy studies, the discrepancies found could be a size-related effect.

  7. Hygroscopic and phase separation properties of ammonium sulfate/organic/water ternary solutions

    NASA Astrophysics Data System (ADS)

    Zawadowicz, M. A.; Proud, S. R.; Seppalainen, S. S.; Cziczo, D. J.

    2015-03-01

    Atmospheric aerosol particles are often partially or completely composed of inorganic salts, such as ammonium sulfate and sodium chloride, and therefore exhibit hygroscopic properties. Many inorganic salts have well-defined deliquescence and efflorescence points at which they take up and lose water, respectively. Deliquescence and efflorescence of simple inorganic salt particles have been investigated by a variety of methods, such as IR spectroscopy, tandem mobility analysis and electrodynamic balance. Field measurements have shown that atmospheric aerosols are not typically pure inorganic salt, instead they often also contain organic species. There is ample evidence from laboratory studies that suggests that mixed particles exist in a phase-separated state, with an aqueous inorganic core and organic shell. Although phase separation has not been measured in situ, there is no reason it would not also take place in the atmosphere. Many recent studies have focused on microscopy techniques that require deposition of the aerosol on a glass slide, possibly changing its surface properties. Here, we investigate the deliquescence and efflorescence points, phase separation and ability to exchange gas-phase components of mixed organic and inorganic aerosol using a flow tube coupled with FTIR spectroscopy. Ammonium sulfate aerosol mixed with organic polyols with different O : C ratios, including 1,4-butanediol, glycerol, 1,2,6-hexanetriol, 1,2-hexanediol, and 1,5-pentanediol have been investigated. Those constituents correspond to materials found in the atmosphere in great abundance, and therefore, particles prepared in this study should mimic atmospheric mixed phase aerosol particles. The results of this study tend to be in agreement with previous microscopy experiments, with several key differences, which possibly reveal a size-dependent effect on phase separation in organic/inorganic aerosol particles.

  8. Nanoscale control over phase separation in conjugated polymer blends using mesoporous silica spheres.

    PubMed

    Kelly, Timothy L; Yano, Kazuhisa; Wolf, Michael O

    2010-01-05

    A method of preparing blended conjugated polymer microparticles using mesoporous silica spheres is described. Poly(3,4-ethylenedioxythiophene) (PEDOT) was blended with poly(furfuryl alcohol) (PFA) by a sequential infiltration-polymerization approach. The materials were evaluated by both scanning and transmission electron microscopy and are shown to retain the overall spherical structure of the silica template. The filling of the mesopores and the polymer distribution within individual particles were determined by a combination of energy-dispersive X-ray microanalysis, X-ray photoelectron spectroscopy, and nitrogen adsorption. The results suggest that when PEDOT is added to the silica host, followed by PFA, the phase separation of the two immiscible polymers is constrained by the dimensions of the silica mesopores, ensuring nanoscale contact between the two phases. The silica template can be removed by etching with 25% hydrofluoric acid, leaving behind a blended polymer microparticle. The etched microparticles exhibit macroporous morphologies different from that of pure PEDOT particles prepared by a similar route. The blended microparticles also appear to undergo limited phase separation; no evidence for distinct polymer domains was observed. Conductivity measurements indicate that the blended particles are above the percolation threshold and support the conclusion that the phase domains are extremely small. Importantly, when PFA is added to the host first, followed by PEDOT, there is a striking difference to the final composition and morphology of the particles. This reversal of the blending order results in a more amorphous, phase-separated material. These results demonstrate the preparation of conjugated polymer blends with engineered nanoscale phase separation and may allow for future improvements in organic device architecture and performance.

  9. Langmuir-Blodgett films of fluorinated glycolipids and polymerizable lipids and their phase separating behavior.

    PubMed

    Scheibe, Patrick; Schoenhentz, Jerome; Platen, Tobias; Hoffmann-Röder, Anja; Zentel, Rudolf

    2010-12-07

    This paper describes the phase separating behavior of Langmuir monolayers from mixtures of different lipids that (i) either carry already a glycopeptide recognition site or can be easily modified to carry one and (ii) polymerizable lipids. To ensure demixing during compression, we used fluorinated lipids for the biological headgroups and hydrocarbon based lipids as polymerizable lipids. As a representative for a lipid monomer, which can be polymerized in the hydrophilic headgroup, a methacrylic monomer was used. As a monomer, which can be polymerized in the hydrophobic tail, a lipid with a diacetylene unit was used (pentacosadiynoic acid, PDA). The fluorinated lipids were on the one hand a perfluorinated lipid with three chains and on the other hand a partially fluorinated lipid with a T(N)-antigen headgroup. The macroscopic phase separation was observed by Brewster angle microscopy, whereas the phase separation on the nanoscale level was observed by atomic force microscopy. It turned out that all lipid mixtures showed (at least) a partial miscibility of the hydrocarbon compounds in the fluorinated compounds. This is positive for pattern formation, as it allows the formation of small demixed 2D patterned structures during crystallization from the homogeneous phase. For miscibility especially a liquid analogue phase proved to be advantageous. As lipid 3 with three fluorinated lipid chains (very stable monolayer) is miscible with the polymerizable lipids 1 and 2, it was mostly used for further investigations. For all three lipid mixtures, a phase separation on both the micrometer and the nanometer level was observed. The size of the crystalline domains could be controlled not only by varying the surface pressure but also by varying the molar composition of the mixtures. Furthermore, we showed that the binary mixture can be stabilized via UV polymerization. After polymerization and subsequent expansion of the barriers, the locked-in polymerized structures are stable

  10. DESIGN AND DEVELOPMENT OF GAS-LIQUID CYLINDRICAL CYCLONE COMPACT SEPARATORS FOR THREE-PHASE FLOW

    SciTech Connect

    Dr. Ram S. Mohan; Dr. Ovadia Shoham

    2000-04-28

    The objective of this five-year project (October, 1997-September, 2002) is to expand the current research activities of Tulsa University Separation Technology Projects (TUSTP) to multiphase oil/water/gas separation. This project will be executed in two phases. Phase I (1997-2000) will focus on the investigations of the complex multiphase hydrodynamic flow behavior in a three-phase Gas-Liquid Cylindrical Cyclone (GLCC{copyright}) Separator. The activities of this phase will include the development of a mechanistic model, a computational fluid dynamics (CFD) simulator, and detailed experimentation on the three-phase GLCC{copyright}. The experimental and CFD simulation results will be suitably integrated with the mechanistic model. In Phase II (2000-2002), the developed GLCC{copyright} separator will be tested under high pressure and real crudes conditions. This is crucial for validating the GLCC{copyright} design for field application and facilitating easy and rapid technology deployment. Design criteria for industrial applications will be developed based on these results and will be incorporated into the mechanistic model by TUSTP. This report presents a brief overview of the activities and tasks accomplished during the first half year (October 1, 1999-March 31, 2000) of the budget period (October 1, 1999-September 30, 2000). The total tasks of the budget period are given initially, followed by the technical and scientific results achieved till date. The report concludes with a detailed description of the plans for the conduct of the project for the second half year (April 1, 2000-September 30, 2000) of the current budget period.

  11. Stability and Oil Migration of Oil-in-Water Emulsions Emulsified by Phase-Separating Biopolymer Mixtures.

    PubMed

    Yang, Nan; Mao, Peng; Lv, Ruihe; Zhang, Ke; Fang, Yapeng; Nishinari, Katsuyoshi; Phillips, Glyn O

    2016-08-01

    Oil-in-water (O/W) emulsions with varying concentration of oil phase, medium-chain triglyceride (MCT), were prepared using phase-separating gum arabic (GA)/sugar beet pectin (SBP) mixture as an emulsifier. Stability of the emulsions including emulsion phase separation, droplet size change, and oil migration were investigated by means of visual observation, droplet size analysis, oil partition analysis, backscattering of light, and interfacial tension measurement. It was found that in the emulsions prepared with 4.0% GA/1.0% SBP, when the concentration of MCT was greater than 2.0%, emulsion phase separation was not observed and the emulsions were stable with droplet size unchanged during storage. This result proves the emulsification ability of phase-separating biopolymer mixtures and their potential usage as emulsifiers to prepare O/W emulsion. However, when the concentration of MCT was equal or less than 2.0%, emulsion phase separation occurred after preparation resulting in an upper SBP-rich phase and a lower GA-rich phase. The droplet size increased in the upper phase whereas decreased slightly in the lower phase with time, compared to the freshly prepared emulsions. During storage, the oil droplets exhibited a complex migration process: first moving to the SBP-rich phase, then to the GA-rich phase and finally gathering at the interface between the two phases. The mechanisms of the emulsion stability and oil migration in the phase-separated emulsions were discussed.

  12. Separation of basic compounds by capillary electrochromatography on an X-Terra RP18 stationary phase.

    PubMed

    Valette, J C; Bizet, A C; Demesmay, C; Rocca, J L; Verdon, E

    2004-09-17

    In this work we demonstrate that the X-Terra RP18 stationary phase, specially designed for the analysis of basic compounds in liquid chromatography, may be successfully used in capillary electrochromatography. Although this packing material does not afford a sufficient electroosmotic flow with classical hydro-organic mobile phases, the addition of a surfactant that adsorbs onto the stationary phase allows to generate a sustainable electroosmosis flow (EOF), the direction of which depends on the charge of the surfactant. The way of manipulating the electroosmotic flow is described (nature and concentration of the added surfactant, proportion of the organic modifier in the mobile phase, pH). It is then demonstrated that high efficiencies can be reached with this packing material (up to 220,000 plates/m with a mean diameter particles of 3.5 microm) when it is operated at high linear velocities. Then the separations of different classes of compounds such as amphenicol antibiotics, macrolide antibiotics or basic test solutes with mobile phases with pH up to 10.8 are described. The influence of the addition of sodium dodcylsulfate (SDS) to the mobile phase on the retention is described and the selectivity of the X-Terra RP18 stationary phase is compared to that of a more traditional phase, i.e. Hypersil C18 stationary phase with SDS added to the mobile phase. However, it is shown that a good repeatability of the retention factors can only be obtained when the ionization of the compounds is totally suppressed since electrolysis of the buffered hydro-organic mobile phase occurs in the buffer reservoirs leading to a variation of the mobile phase pH and consequently to a modification of the ionization degree of the solutes having their pKa close to the mobile phase pH.

  13. Graphitic carbon nitride as high-resolution stationary phase for gas chromatographic separations.

    PubMed

    Zheng, Yunzhong; Qi, Meiling; Fu, Ruonong

    2016-07-08

    This work presents the first example of utilization of graphitic carbon nitride (g-C3N4) as stationary phase for capillary gas chromatographic (GC) separations. The statically coated g-C3N4 column showed the column efficiencies of 3760 plates/m and weak polarity. Its resolving capability and retention behaviours were investigated by using the Grob test mixture, and mixtures of diverse types of analytes, and structural and positional isomers. The results showed superior separation performance of the g-C3N4 stationary phase for some critical analytes and preferential retention for aromatic analytes. Specifically, it exhibited high-resolution capability for aromatic and aliphatic isomers such as methylnaphthalenes and dimethylnaphthalenes, phenanthrene and anthracene and alkane isomers. In addition, g-C3N4 column showed excellent thermal stability up to 280°C and good repeatability with relative standard deviation (RSD) values less than 0.09% for intra-day, below 0.23% for inter-day and in the range of 1.9-8.4% for between-column, respectively. The advantageous separation performance shows the potential of g-C3N4 and related materials as stationary phase in GC and other separation technologies.

  14. Modeling and simulation of steady state model approach for horizontal three phase separator (HTPS)

    NASA Astrophysics Data System (ADS)

    Triwibowo, Bayu; Prasetiawan, Haniif; Hisyam, Anwaruddin; Fauzan, Mohammad Fariz; Rizky, Muhammad Habib Fahd

    2017-03-01

    Main function of oil production facility is to separate oil well stream into three phases i.e. oil, gas and water. A vessel called three phase separator is used for this purpose, commonly in horizontal arrangement. In order to optimize the process, an accurate model for horizontal three phase separator (HTPS) is needed. Computational Fluid Dynamics (CFD) is a mathematical tool capable of simulating a wide range of fluid flows. HTPS dimensions used in this simulation were taken from one of oil and gas company in Indonesia. The CFD simulation used in this study is based on volume of fluid and k-ɛ turbulence models. Gas outlet was assumed using porous media zone model with fluid porosity 0.99. Simulation result displayed concentration and velocity distribution for each component inside HTPS. The result of concentration distribution shows that the region of fluid divided into upper region and lower region. The lower region major component were water and upper region mainly consist of gas and oil. The contour of concentration distribution indicated a good separation process with distribution of water flow rate at the outlet of water, oil, and gas respectively are 405,67; 115,65; and 172.01 lb/min

  15. Oscillating phase separation in microemulsions. II. Description by a bending free energy

    NASA Astrophysics Data System (ADS)

    Vollmer, Jürgen; Vollmer, Doris; Strey, Reinhard

    1997-09-01

    We propose a mechanism to describe the phase separation of a single phase of water-in-oil microemulsion droplets towards a phase of smaller water droplets coexisting with a water-rich excess phase. The phase separation shows oscillatory behavior when induced by a continuous temperature increase. A periodic clouding and clearing is observed in the extinction of transmitted light which is also reflected in the specific heat. To model this behavior the bending free energy describing the equilibrium phase transition is applied to identify the energy barriers in the dynamics of this transition. They are due to conservation laws preventing the relaxation to a close to equilibrium size distribution of droplets unless volume and surface is redistributed simultaneously for a large number of droplets. By numerical integration of an expression for the time evolution of the size distribution of droplets it is verified that constant heating gives rise to oscillations. Besides clarifying the origin of the oscillations this approach also gives good estimates for heat absorbed during a single oscillation.

  16. Search for improved fluorinated stationary phases for separation of fluorine-containing pharmaceuticals from their desfluoro analogs.

    PubMed

    Regalado, Erik L; Makarov, Alexey A; McClain, Ray; Przybyciel, Matthew; Welch, Christopher J

    2015-02-06

    Evaluation of a several fluorine-containing stationary phases for the chromatographic separation of fluorine-containing pharmaceuticals from their corresponding desfluoro analogs revealed a number of perfluoroaryl and perfluoroalky stationary phases that afford good separations. These fluorous stationary phases exhibit greater retention for the fluorine-containing compounds relative to the H-containing analogs, consistent with a fluorophilic retention mechanism. While both perfluoroalkyl and perfluoroaryl stationary phases afford adequate resolution, the perfluoroaryl columns generally exhibit superior separation factor (α) and peak efficiency (N), resulting in faster baseline separations, with the Hypersil Gold PFP and Poroshell 120 PFP columns providing the best overall performance for the test group studied.

  17. Morphology Mapping of Phase-Separated Polymer Films Using Nanothermal Analysis

    SciTech Connect

    Nikiforov, Maxim; Gam, Sangah; Jesse, Stephen; Composto, Russel C; Kalinin, Sergei V

    2010-01-01

    Polymers films are attractive, in part, because their physical properties can be tuned by blending polymer with complementary characteristics. However, blending is typically challenging because most polymers will undergo phase separation, resulting in unpredictable behavior. Here, we introduce band excitation nanothermal analysis (BE-NanoTA) as a nondestructive AFM-based technique for mapping the near surface, thermal properties of polymeric coatings. BE-NanoTA was used to investigate phase separation and domain growth in poly(styrene-ran-acrylonitrile):poly(methyl methacrylate) SAN:PMMA films. The size and shape of PMMA-rich domains are consistent with prior measurements on the same system using a destructive method, namely UV-ozone etching of PMMA followed by topography mapping using standard AFM. Moreover, new insights into the mechanism of phase separation were uncovered including the observation of SAN- and PMMA-rich channels near the surface at early times as well as small SAN-rich domains trapped within large PMMA domains during intermediate times. Because it is nondestructive, BE-NanoTA can be used to explore in situ phase evolution in soft matter systems (e.g., polymer nanocomposites) which do not lend themselves to the UV-ozone etching method

  18. Surface modification of polytetrafluoroethylene column for two-stationary phase separations by counter-current chromatography.

    PubMed

    Quan, Kai-jun; Huang, Xin-yi; Li, Xiao-ting; Wang, Gao-hong; Liu, Yan-juan; Duan, Wen-da; Di, Duo-long

    2015-11-27

    To improve the separation capability of CCC, a novel solid-liquid two-stationary phases CCC (ASP-CCC) column was prepared employing graphene oxide (GO) conjugated poly-dopamine (PD) coating (GO/PD) as auxiliary stationary phase (ASP). The results of Scanning electron microscopy (SEM), contact angle and X-ray photoelectron spectroscopy (XPS) indicated that nanostructured GO and PD were successfully grafted on the inner wall of the PTFE column. Three alkaloid compounds were selected as the target analytes to evaluate the performance of the novel column. Because of the intermolecular force (hydrogen bond, electrostatic interaction and π-π interaction) between the ASP and model compounds, three analytes were well separated with this novel ASP-CCC column. Additionally, the novel column exhibited higher stationary phase retention ratio, about 8%, than original column without changing the chromatographic condition. Furthermore, the eluotropic sequence of analytes on novel column was in accordance with that in the original column. This suggested that the novel column is a CCC column with auxiliary stationary phase (ASP) in its own right, and the present separation mode is the combination of partition chromatography and adsorption chromatography.

  19. Liquid-liquid phase separation in aerosol particles: Imaging at the Nanometer Scale

    SciTech Connect

    O'Brien, Rachel; Wang, Bingbing; Kelly, Stephen T.; Lundt, Nils; You, Yuan; Bertram, Allan K.; Leone, Stephen R.; Laskin, Alexander; Gilles, Mary K.

    2015-04-21

    Atmospheric aerosols can undergo phase transitions including liquid-liquid phase separation (LLPS) while responding to changes in the ambient relative humidity (RH). Here, we report results of chemical imaging experiments using environmental scanning electron microscopy (ESEM) and scanning transmission x-ray microscopy (STXM) to investigate the LLPS of micron sized particles undergoing a full hydration-dehydration cycle. Internally mixed particles composed of ammonium sulfate (AS) and either: limonene secondary organic carbon (LSOC), a, 4-dihydroxy-3-methoxybenzeneaceticacid (HMMA), or polyethylene glycol (PEG-400) were studied. Events of LLPS with apparent core-shell particle morphology were observed for all samples with both techniques. Chemical imaging with STXM showed that both LSOC/AS and HMMA/AS particles were never homogeneously mixed for all measured RH’s above the deliquescence point and that the majority of the organic component was located in the shell. The shell composition was estimated as 65:35 organic: inorganic in LSOC/AS and as 50:50 organic: inorganic for HMMA/AS. PEG-400/AS particles showed fully homogeneous mixtures at high RH and phase separated below 89-92% RH with an estimated 50:50% organic to inorganic mix in the shell. These two chemical imaging techniques are well suited for in-situ analysis of the hygroscopic behavior, phase separation, and surface composition of collected ambient aerosol particles.

  20. MPP1 as a Factor Regulating Phase Separation in Giant Plasma Membrane-Derived Vesicles

    PubMed Central

    Podkalicka, Joanna; Biernatowska, Agnieszka; Majkowski, Michał; Grzybek, Michał; Sikorski, Aleksander F.

    2015-01-01

    The existence of membrane-rafts helps to conceptually understand the spatiotemporal organization of membrane-associated events (signaling, fusion, fission, etc.). However, as rafts themselves are nanoscopic, dynamic, and transient assemblies, they cannot be directly observed in a metabolizing cell by traditional microscopy. The observation of phase separation in giant plasma membrane-derived vesicles from live cells is a powerful tool for studying lateral heterogeneity in eukaryotic cell membranes, specifically in the context of membrane rafts. Microscopic phase separation is detectable by fluorescent labeling, followed by cooling of the membranes below their miscibility phase transition temperature. It remains unclear, however, if this lipid-driven process is tuneable in any way by interactions with proteins. Here, we demonstrate that MPP1, a member of the MAGUK family, can modulate membrane properties such as the fluidity and phase separation capability of giant plasma membrane-derived vesicles. Our data suggest that physicochemical domain properties of the membrane can be modulated, without major changes in lipid composition, through proteins such as MPP1. PMID:25954878

  1. Evidence that oleic acid exists in a separate phase within stratum corneum lipids

    SciTech Connect

    Ongpipattanakul, B.; Burnette, R.R.; Potts, R.O.; Francoeur, M.L. )

    1991-03-01

    Oleic acid is known to be a penetration enhancer for polar to moderately polar molecules. A mechanism related to lipid phase separation has been previously proposed by this laboratory to explain the increases in skin transport. In the studies presented here, Fourier transform infrared spectroscopy (FT-IR) was utilized to investigate whether or not oleic acid exists in a separate phase within stratum corneum (SC) lipids. Per-deuterated oleic acid was employed allowing the conformational phase behavior of the exogenously added fatty acid and the endogenous SC lipids to be monitored independently of each other. The results indicated that oleic acid exerts a significant effect on the SC lipids, lowering the lipid transition temperature (Tm) in addition to increasing the conformational freedom or flexibility of the endogenous lipid alkyl chains above their Tm. At temperatures lower than Tm, however, oleic acid did not significantly change the chain disorder of the SC lipids. Similar results were obtained with lipids isolated from the SC by chloroform:methanol extraction. Oleic acid, itself, was almost fully disordered at temperatures both above and below the endogenous lipid Tm in the intact SC and extracted lipid samples. This finding suggested that oleic acid does exist as a liquid within the SC lipids. The coexistence of fluid oleic acid and ordered SC lipids, at physiological temperatures, is consistent with the previously proposed phase-separation transport mechanism for enhanced diffusion.

  2. Dual Phase Separation for Synthesis of Bimodal Meso/Macroporous Carbon Monoliths

    SciTech Connect

    Liang, Chengdu; Dai, Sheng

    2009-01-01

    Polymerization-induced spinodal decomposition was conducted in glycolic solutions of phloroglucinol/formaldehyde (PF) copolymer and poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) to synthesize bicontinuous macroporous morphologies with micro-domains from 0.5 to 6 microns. The polymeric materials were further carbonized at elevated temperature to yield bimodal meso/macroporous carbon monoliths after the thermal decomposition of the PEO-PPO-PEO template. The bimodal porous nature of the resultant carbon monoliths resulted from the dual phase separation, in which spinodal decomposition and microphase separation occurred simultaneously. We demonstrated the tunability of macropores without alteration of mesopore sizes.

  3. Zero-g experiments with a He II active phase separator for space application

    NASA Astrophysics Data System (ADS)

    Denner, H. D.; Klipping, G.; Lueders, K.; Ruppert, U.; Stahnke, F.; Szuecs, Z.; Elleman, D.; Petrac, D.

    An active phase separator (APS) for temperature control of He II space cooling systems was tested in a zero-g environment during a series of parabolic flights on a NASA KC 135 aircraft. The APS provides for liquid-gas separation and features an annular gap, a downstream heat exchanger and an upstream ball closure. The apparatus was operated during acceleration and floating and in two different heat load situations. The tests confirmed that adequate mass flow rates could be maintained using a vacuum pump to simulate space vacuum and that residual liquid could be evaporated from the heat exchanger after closing a ball valve to seal off flows.

  4. Crystal growth in a three-phase system: Diffusion and liquid-liquid phase separation in lysozyme crystal growth

    NASA Astrophysics Data System (ADS)

    Heijna, M. C. R.; van Enckevort, W. J. P.; Vlieg, E.

    2007-07-01

    In the phase diagram of the protein hen egg-white lysozyme, a region is present in which the lysozyme solution demixes and forms two liquid phases. In situ observations by optical microscopy show that the dense liquid droplets dissolve when crystals grow in this system. During this process the demixed liquid region retracts from the crystal surface. The spatial distribution of the dense phase droplets present special boundary conditions for Fick’s second law for diffusion. In combination with the cylindrical symmetry provided by the kinetically roughened crystals, this system allows for a full numerical analysis. Using experimental data for setting the boundary conditions, a quasi-steady-state solution for the time-dependent concentration profile was shown to be valid. Comparison of kinetically rough growth in a phase separated system and in a nonseparated system shows that the growth kinetics for a three-phase system differs from a two-phase system, in that crystals grow more slowly but the duration of growth is prolonged.

  5. Crystal growth in a three-phase system: diffusion and liquid-liquid phase separation in lysozyme crystal growth.

    PubMed

    Heijna, M C R; van Enckevort, W J P; Vlieg, E

    2007-07-01

    In the phase diagram of the protein hen egg-white lysozyme, a region is present in which the lysozyme solution demixes and forms two liquid phases. In situ observations by optical microscopy show that the dense liquid droplets dissolve when crystals grow in this system. During this process the demixed liquid region retracts from the crystal surface. The spatial distribution of the dense phase droplets present special boundary conditions for Fick's second law for diffusion. In combination with the cylindrical symmetry provided by the kinetically roughened crystals, this system allows for a full numerical analysis. Using experimental data for setting the boundary conditions, a quasi-steady-state solution for the time-dependent concentration profile was shown to be valid. Comparison of kinetically rough growth in a phase separated system and in a nonseparated system shows that the growth kinetics for a three-phase system differs from a two-phase system, in that crystals grow more slowly but the duration of growth is prolonged.

  6. Investigation of phase separation behavior and formation of plasmonic nanocomposites from polypeptide-gold nanorod nanoassemblies.

    PubMed

    Huang, Huang-Chiao; Nanda, Alisha; Rege, Kaushal

    2012-04-24

    Genetically engineered elastin-like polypeptides (ELP) can be interfaced with cetyltrimethyl ammonium bromide (CTAB)-stabilized gold nanorods (GNRs) resulting in the formation of stable dispersions (nanoassemblies). Increasing the dispersion temperature beyond the ELP transition temperature results in phase separation and formation of solid-phase ELP-GNR matrices (nanocomposites). Here, we investigated different physicochemical conditions that influence nanocomposite formation from temperature-induced phase separation of ELP-GNR nanoassemblies. The presence of cetyltrimethyl ammonium bromide (CTAB), used to template the formation of gold nanorods, plays a significant role in the phase separation behavior, with high concentrations of the surfactant leading to dramatic enhancements in ELP transition temperature. Nanocomposites could be generated at 37 °C in the presence of low CTAB concentrations (<1.5 mM); higher concentrations of CTAB necessitated higher temperatures (60 °C) due to elevated transition temperatures. The concentration of gold nanorods, however, had minimal influence on the phase separation behavior and nanocomposite formation. Further analysis of the kinetics of nanocomposite formation using a mathematical model indicated that CTAB largely influenced the early event of coacervation of ELP-GNR nanoassemblies leading to nanocomposites, but had minimal effect on nanocomposite maturation, which is a later-stage longer event. Finally, nanocomposites prepared in the presence of low CTAB concentrations demonstrated a superior photothermal response following laser irradiation compared to those generated using higher CTAB concentrations. Our results on understanding the formation of plasmonic/photothermal ELP-GNR nanocomposites have significant implications for tissue engineering, regenerative medicine, and drug delivery.

  7. The effect of charge separation on the phase behavior of dipolar colloidal rods.

    PubMed

    Rutkowski, David M; Velev, Orlin D; Klapp, Sabine H L; Hall, Carol K

    2016-06-14

    Colloids with anisotropic shape and charge distribution can assemble into a variety of structures that could find use as novel materials for optical, photonic, electronic and structural applications. Because experimental characterization of the many possible types of multi-shape and multipolar colloidal particles that could form useful structures is difficult, the search for novel colloidal materials can be enhanced by simulations of colloidal particle assembly. We have simulated a system of dipolar colloidal rods at fixed aspect ratio using discontinuous molecular dynamics (DMD) to investigate how the charge separation of an embedded dipole affects the types of assemblies that occur. Each dipolar rod is modeled as several overlapping spheres fixed in an elongated shape to represent excluded volume and two smaller, embedded spheres to represent the charges that make up the extended dipole. Large charge separations predominately form structures where the rods link head-to-tail while small charge separations predominately form structures where the rods stack side-by-side. Rods with small charge separations tend to form dense aggregates while rods with large charge separations tend to form coarse gel-like structures. Structural phase boundaries between fluid, string-fluid, and "gel" (networked) phases are mapped out and characterized as to whether they have global head-to-tail or global side-by-side order. A structural coarsening transition is observed for particles with large charge separations in which the head-tail networks thicken as temperature is lowered due to an increased tendency to form side-by-side structures. Triangularly connected networks form at small charge separations; these may be useful for encapsulating smaller particles.

  8. Rapid variations in fluid chemistry constrain hydrothermal phase separation at the Main Endeavour Field

    NASA Astrophysics Data System (ADS)

    Love, Brooke; Lilley, Marvin; Butterfield, David; Olson, Eric; Larson, Benjamin

    2017-02-01

    Previous work at the Main Endeavour Field (MEF) has shown that chloride concentration in high-temperature vent fluids has not exceeded 510 mmol/kg (94% of seawater), which is consistent with brine condensation and loss at depth, followed by upward flow of a vapor phase toward the seafloor. Magmatic and seismic events have been shown to affect fluid temperature and composition and these effects help narrow the possibilities for sub-surface processes. However, chloride-temperature data alone are insufficient to determine details of phase separation in the upflow zone. Here we use variation in chloride and gas content in a set of fluid samples collected over several days from one sulfide chimney structure in the MEF to constrain processes of mixing and phase separation. The combination of gas (primarily magmatic CO2 and seawater-derived Ar) and chloride data, indicate that neither variation in the amount of brine lost, nor mixing of the vapor phase produced at depth with variable quantities of (i) brine or (ii) altered gas rich seawater that has not undergone phase separation, can explain the co-variation of gas and chloride content. The gas-chloride data require additional phase separation of the ascending vapor-like fluid. Mixing and gas partitioning calculations show that near-critical temperature and pressure conditions can produce the fluid compositions observed at Sully vent as a vapor-liquid conjugate pair or as vapor-liquid pair with some remixing, and that the gas partition coefficients implied agree with theoretically predicted values.Plain Language SummaryWhen the chemistry of fluids from deep sea hot springs changes over a short time span, it allows us to narrow down the conditions and processes that created those fluids. This gives us a better idea what is happening under the seafloor where the water is interacting with hot rocks and minerals, boiling, and taking on the character it will have when it emerges at</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23554360','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23554360"><span>Selectivity differences of water-soluble vitamins <span class="hlt">separated</span> on hydrophilic interaction stationary <span class="hlt">phases</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yang, Yuanzhong; Boysen, Reinhard I; Hearn, Milton T W</p> <p>2013-06-01</p> <p>In this study, the retention behavior and selectivity differences of water-soluble vitamins were evaluated with three types of polar stationary <span class="hlt">phases</span> (i.e. an underivatized silica <span class="hlt">phase</span>, an amide <span class="hlt">phase</span>, and an amino <span class="hlt">phase</span>) operated in the hydrophilic interaction chromatographic mode with ESI mass spectrometric detection. The effects of mobile <span class="hlt">phase</span> composition, including buffer pH and concentration, on the retention and selectivity of the vitamins were investigated. In all stationary <span class="hlt">phases</span>, the neutral or weakly charged vitamins exhibited very weak retention under each of the pH conditions, while the acidic and more basic vitamins showed diverse retention behaviors. With the underivatized silica <span class="hlt">phase</span>, increasing the salt concentration of the mobile <span class="hlt">phase</span> resulted in enhanced retention of the acidic vitamins, but decreased retention of the basic vitamins. These observations thus signify the involvement of secondary mechanisms, such as electrostatic interaction in the retention of these analytes. Under optimized conditions, a baseline <span class="hlt">separation</span> of all vitamins was achieved with excellent peak efficiency. In addition, the effects of water content in the sample on retention and peak efficiency were examined, with sample stacking effects observed when the injected sample contained a high amount of water.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17595947','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17595947"><span>Superheated water as chromatographic eluent for parabens <span class="hlt">separation</span> on octadecyl coated zirconia stationary <span class="hlt">phase</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Dugo, Paola; Buonasera, Katia; Crupi, Maria Lucia; Cacciola, Francesco; Dugo, Giovanni; Mondello, Luigi</p> <p>2007-05-01</p> <p>In this study, the use of pure water at superheated temperatures, between 100 and 200 degrees C, as a mobile <span class="hlt">phase</span> for RP <span class="hlt">separation</span> is explored. Instrumental parameters, such as temperature, flow rate, preheating and cooling, have shown significant effects on the quality of the chromatographic peaks. The properties of superheated water as an eluent were investigated by observing the chromatographic behaviour of four parabens on a carbon-clad zirconia (ZR) <span class="hlt">phase</span> with covalently bonded octadecyl groups. Results were compared with those obtained at 30 degrees C on a silica-based <span class="hlt">phase</span> with octadecyl groups, using water and ACN as mobile <span class="hlt">phase</span>. The optimized method was finally applied to analyse parabens in a commercial body cream.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24033058','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24033058"><span>Anisotropic electronic state via spontaneous <span class="hlt">phase</span> <span class="hlt">separation</span> in strained vanadium dioxide films.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, M K; Wagner, M; Abreu, E; Kittiwatanakul, S; McLeod, A; Fei, Z; Goldflam, M; Dai, S; Fogler, M M; Lu, J; Wolf, S A; Averitt, R D; Basov, D N</p> <p>2013-08-30</p> <p>We resolved the enigma of anisotropic electronic transport in strained vanadium dioxide (VO2) films by inquiring into the role that strain plays in the nanoscale <span class="hlt">phase</span> <span class="hlt">separation</span> in the vicinity of the insulator-to-metal transition. The root source of the anisotropy was visualized as the formation of a peculiar unidirectional stripe state which accompanies the <span class="hlt">phase</span> transition. Furthermore, nanoscale infrared spectroscopy unveils distinct facets of electron-lattice interplay at three different stages of the <span class="hlt">phase</span> transition. These stages include the initial formation of sparse nonpercolating metallic domains without noticeable involvement of the lattice followed by an electron-lattice coupled anisotropic stripe state close to percolation which ultimately evolves into a nearly isotropic rutile metallic <span class="hlt">phase</span>. Our results provide a unique mesoscopic perspective for the tunable macroscopic phenomena in strained metal oxide films.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013PhRvL.111i6602L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013PhRvL.111i6602L"><span>Anisotropic Electronic State via Spontaneous <span class="hlt">Phase</span> <span class="hlt">Separation</span> in Strained Vanadium Dioxide Films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liu, M. K.; Wagner, M.; Abreu, E.; Kittiwatanakul, S.; McLeod, A.; Fei, Z.; Goldflam, M.; Dai, S.; Fogler, M. M.; Lu, J.; Wolf, S. A.; Averitt, R. D.; Basov, D. N.</p> <p>2013-08-01</p> <p>We resolved the enigma of anisotropic electronic transport in strained vanadium dioxide (VO2) films by inquiring into the role that strain plays in the nanoscale <span class="hlt">phase</span> <span class="hlt">separation</span> in the vicinity of the insulator-to-metal transition. The root source of the anisotropy was visualized as the formation of a peculiar unidirectional stripe state which accompanies the <span class="hlt">phase</span> transition. Furthermore, nanoscale infrared spectroscopy unveils distinct facets of electron-lattice interplay at three different stages of the <span class="hlt">phase</span> transition. These stages include the initial formation of sparse nonpercolating metallic domains without noticeable involvement of the lattice followed by an electron-lattice coupled anisotropic stripe state close to percolation which ultimately evolves into a nearly isotropic rutile metallic <span class="hlt">phase</span>. Our results provide a unique mesoscopic perspective for the tunable macroscopic phenomena in strained metal oxide films.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004JPhA...37.3769L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004JPhA...37.3769L"><span>New kind of <span class="hlt">phase</span> <span class="hlt">separation</span> in a CA traffic model with anticipation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lárraga, M. E.; del Río, J. A.; Schadschneider, A.</p> <p>2004-03-01</p> <p>A cellular automaton model of traffic flow taking into account velocity anticipation is introduced. The strength of anticipation can be varied to describe different driving schemes. We find a new <span class="hlt">phase</span> <span class="hlt">separation</span> into a free-flow regime and a so-called v-platoon in an intermediate density regime. In a v-platoon all cars move with velocity v and have vanishing headway. The velocity v of a platoon only depends on the strength of anticipation. At high densities, a congested state characterized by the coexistence of a 0-platoon with several v-platoons is reached. The results are not only relevant for automated highway systems, but also help to elucidate the effects of anticipation that play an essential role in realistic traffic models. From a physics point of view the model is interesting because it exhibits <span class="hlt">phase</span> <span class="hlt">separation</span> with a condensed <span class="hlt">phase</span> in which particles move coherently with finite velocity coexisting with either a non-condensed (free-flow) <span class="hlt">phase</span> or another condensed <span class="hlt">phase</span> that is non-moving.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011PhDT........13O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011PhDT........13O"><span>The rheology and <span class="hlt">phase</span> <span class="hlt">separation</span> kinetics of mixed-matrix membrane dopes</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Olanrewaju, Kayode Olaseni</p> <p></p> <p>Mixed-matrix hollow fiber membranes are being developed to offer more efficient gas <span class="hlt">separations</span> applications than what the current technologies allow. Mixed-matrix membranes (MMMs) are membranes in which molecular sieves incorporated in a polymer matrix enhance <span class="hlt">separation</span> of gas mixtures based on the molecular size difference and/or adsorption properties of the component gases in the molecular sieve. The major challenges encountered in the efficient development of MMMs are associated with some of the paradigm shifts involved in their processing, as compared to pure polymer membranes. For instance, mixed-matrix hollow fiber membranes are prepared by a dry-wet jet spinning method. Efficient large scale processing of hollow fibers by this method requires knowledge of two key process variables: the rheology and kinetics of <span class="hlt">phase</span> <span class="hlt">separation</span> of the MMM dopes. Predicting the rheological properties of MMM dopes is not trivial; the presence of particles significantly affects neat polymer membrane dopes. Therefore, the need exists to characterize and develop predictive capabilities for the rheology of MMM dopes. Furthermore, the kinetics of <span class="hlt">phase</span> <span class="hlt">separation</span> of polymer solutions is not well understood. In the case of MMM dopes, the kinetics of <span class="hlt">phase</span> <span class="hlt">separation</span> are further complicated by the presence of porous particles in a polymer solution. Thus, studies on the <span class="hlt">phase</span> <span class="hlt">separation</span> kinetics of polymer solutions and suspensions of zeolite particles in polymer solutions are essential. Therefore, this research thesis aims to study the rheology and <span class="hlt">phase</span> <span class="hlt">separation</span> kinetics of mixed-matrix membrane dopes. In our research efforts to develop predictive models for the shear rheology of suspensions of zeolite particles in polymer solutions, it was found that MFI zeolite suspensions have relative viscosities that dramatically exceed the Krieger-Dougherty predictions for hard sphere suspensions. Our investigations showed that the major origin of this discrepancy is the selective</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1998PhRvE..58.1211A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1998PhRvE..58.1211A"><span>Liquid-crystal-anchoring transitions at surfaces created by polymerization-induced <span class="hlt">phase</span> <span class="hlt">separation</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Amundson, Karl R.; Srinivasarao, Mohan</p> <p>1998-08-01</p> <p>A surface anchoring transition of a nematic at polymer surfaces created by polymerization-induced <span class="hlt">phase</span> <span class="hlt">separation</span> is presented. This transition is unusual in that it occurs far from bulk nematic <span class="hlt">phase</span> transitions and it is tunable across nearly the entire nematic temperature range by modification of the polymer side group. Anchoring behavior is qualitatively understood by considerating enthalpic and entropic contributions to surface energy. Interesting behavior of some polymer-dispersed liquid-crystal films is explained, and observations provide a pathway to control properties.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/21386741','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/21386741"><span><span class="hlt">Phase</span> <span class="hlt">separation</span> and pairing regimes in the one-dimensional asymmetric Hubbard model</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Barbiero, L.; Casadei, M.; Dalmonte, M.; Ercolessi, E.; Ortolani, F.</p> <p>2010-06-01</p> <p>We address some open questions regarding the <span class="hlt">phase</span> diagram of the one-dimensional Hubbard model with asymmetric hopping coefficients and balanced species. In the attractive regime we present a numerical study of the passage from on-site pairing dominant correlations at small asymmetries to charge-density waves in the region with markedly different hopping coefficients. In the repulsive regime we exploit two analytical treatments in the strong- and weak-coupling regimes in order to locate the onset of <span class="hlt">phase</span> <span class="hlt">separation</span> at small and large asymmetries, respectively.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017PhRvL.118i8002S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017PhRvL.118i8002S"><span>Small Activity Differences Drive <span class="hlt">Phase</span> <span class="hlt">Separation</span> in Active-Passive Polymer Mixtures</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Smrek, Jan; Kremer, Kurt</p> <p>2017-03-01</p> <p>Recent theoretical studies found that mixtures of active and passive colloidal particles <span class="hlt">phase</span> <span class="hlt">separate</span> but only at very high activity ratio. The high value poses serious obstacles for experimental exploration of this phenomenon. Here we show using simulations that when the active and passive particles are polymers, the critical activity ratio decreases with the polymer length. This not only facilitates the experiments but also has implications on the DNA organization in living cell nuclei. Entropy production can be used as an accurate indicator of this nonequilibrium <span class="hlt">phase</span> transition.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4561857','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4561857"><span><span class="hlt">Separation</span> of Quadruplex Polymorphism in DNA Sequences by Reversed-<span class="hlt">Phase</span> Chromatography</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Miller, M. Clarke; Ohrenberg, Carl J.; Kuttan, Ashani; Trent, John O.</p> <p>2015-01-01</p> <p>This unit describes a method for the <span class="hlt">separation</span> of a mixture of quadruplex conformations formed from the same parent sequence via reversed-<span class="hlt">phase</span> chromatography (RPC). Polymorphism is inherent to quadruplex formation and even relatively simple quadruplex-forming sequences can fold into a cornucopia of possible conformations and topologies. Isolation of a specific conformation for study can be problematic. This is especially true for conformations of the human telomere sequence d(GGG(TTAGGG)3), High Performance Liquid Chromatography (HPLC), especially reversed-<span class="hlt">phase</span> chromatography, has been a mainstay of nucleic acids research and purification for many decades. We have successfully applied this method to the problem of <span class="hlt">separating</span> individual quadruplex species in the ensemble from the same parent sequence. PMID:26344226</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPhD...50h5007L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPhD...50h5007L"><span>Magnetically induced nonvolatile magnetoresistance and resistance memory effect in <span class="hlt">phase-separated</span> manganite thin films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Li, Qian; Cao, Qingqi; Wang, Dunhui; Du, Youwei</p> <p>2017-03-01</p> <p>We report the observation of magnetically induced resistance memory effect in a typical electronic <span class="hlt">phase-separated</span> manganite La5/8‑x Pr x Ca3/8MnO3 (x  =  0.3) thin film. In the hysteresis region of metal-to-insulator transition, the resistance exhibits a sharp drop with the application of magnetic field and maintains the low resistance state after the removal of field, showing a nonvolatile magnetoresistance effect. The high resistance state can be recovered until the temperature is warmed. More explicit measurements at the hysteresis region exhibit the non-volatility and irreversibility of magnetoresistance, which can be ascribed to the percolative feature in the electronic <span class="hlt">phase-separated</span> manganite. The origin and potential applications of these interesting effects are discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014ARPC...65...59T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014ARPC...65...59T"><span><span class="hlt">Phase</span> <span class="hlt">Separation</span> in Bulk Heterojunctions of Semiconducting Polymers and Fullerenes for Photovoltaics</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Treat, Neil D.; Chabinyc, Michael L.</p> <p>2014-04-01</p> <p>Thin-film solar cells are an important source of renewable energy. The most efficient thin-film solar cells made with organic materials are blends of semiconducting polymers and fullerenes called the bulk heterojunction (BHJ). Efficient BHJs have a nanoscale <span class="hlt">phase-separated</span> morphology that is formed during solution casting. This article reviews recent work to understand the nature of the <span class="hlt">phase-separation</span> process resulting in the formation of the domains in polymer-fullerene BHJs. The BHJ is now viewed as a mixture of polymer-rich, fullerene-rich, and mixed polymer-fullerene domains. The formation of this structure can be understood through fundamental knowledge of polymer physics. The implications of this structure for charge transport and charge generation are given.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_19 --> <div id="page_20" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="381"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16090140','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16090140"><span>Smoothed particle hydrodynamics model for <span class="hlt">phase</span> <span class="hlt">separating</span> fluid mixtures. I. General equations.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Thieulot, Cedric; Janssen, L P B M; Español, Pep</p> <p>2005-07-01</p> <p>We present a thermodynamically consistent discrete fluid particle model for the simulation of a recently proposed set of hydrodynamic equations for a <span class="hlt">phase</span> <span class="hlt">separating</span> van der Waals fluid mixture [P. Español and C.A.P. Thieulot, J. Chem. Phys. 118, 9109 (2003)]. The discrete model is formulated by following a discretization procedure given by the smoothed particle hydrodynamics (SPH) method within the thermodynamically consistent general equation for the nonequilibrium reversible-irreversible coupling (GENERIC) framework. Each fluid particle carries information on the mass, momentum, energy, and the mass fraction of the different components. The discrete model allows one to simulate nonisothermal dynamic evolution of <span class="hlt">phase</span> <span class="hlt">separating</span> fluids with surface tension effects while respecting the first and second laws of thermodynamics exactly.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005PhRvE..72a6713T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005PhRvE..72a6713T"><span>Smoothed particle hydrodynamics model for <span class="hlt">phase</span> <span class="hlt">separating</span> fluid mixtures. I. General equations</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Thieulot, Cedric; Janssen, L. P. B. M.; Español, Pep</p> <p>2005-07-01</p> <p>We present a thermodynamically consistent discrete fluid particle model for the simulation of a recently proposed set of hydrodynamic equations for a <span class="hlt">phase</span> <span class="hlt">separating</span> van der Waals fluid mixture [P. Español and C.A.P. Thieulot, J. Chem. Phys. 118, 9109 (2003)]. The discrete model is formulated by following a discretization procedure given by the smoothed particle hydrodynamics (SPH) method within the thermodynamically consistent general equation for the nonequilibrium reversible-irreversible coupling (GENERIC) framework. Each fluid particle carries information on the mass, momentum, energy, and the mass fraction of the different components. The discrete model allows one to simulate nonisothermal dynamic evolution of <span class="hlt">phase</span> <span class="hlt">separating</span> fluids with surface tension effects while respecting the first and second laws of thermodynamics exactly.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5015022','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5015022"><span>Synthesis of semicrystalline nanocapsular structures obtained by Thermally Induced <span class="hlt">Phase</span> <span class="hlt">Separation</span> in nanoconfinement</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Torino, Enza; Aruta, Rosaria; Sibillano, Teresa; Giannini, Cinzia; Netti, Paolo A.</p> <p>2016-01-01</p> <p><span class="hlt">Phase</span> <span class="hlt">separation</span> of a polymer solution exhibits a peculiar behavior when induced in a nanoconfinement. The energetic constraints introduce additional interactions between the polymer segments that reduce the number of available configurations. In our work, this effect is exploited in a one-step strategy called nanoconfined-Thermally Induced <span class="hlt">Phase</span> <span class="hlt">Separation</span> (nc-TIPS) to promote the crystallization of polymer chains into nanocapsular structures of controlled size and shell thickness. This is accomplished by performing a quench step of a low-concentrated PLLA-dioxane-water solution included in emulsions of mean droplet size <500 nm acting as nanodomains. The control of nanoconfinement conditions enables not only the production of nanocapsules with a minimum mean particle diameter of 70 nm but also the tunability of shell thickness and its crystallinity degree. The specific properties of the developed nanocapsular architectures have important implications on release mechanism and loading capability of hydrophilic and lipophilic payload compounds. PMID:27604818</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012PhDT........31X','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012PhDT........31X"><span><span class="hlt">Separation</span> of basic oligopeptides by ion-pairing reversed-<span class="hlt">phase</span> chromatography</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Xie, Wenchun</p> <p></p> <p>The present thesis consist of five chapters. Chapter I introduces background information on the ion-pairing reversed-<span class="hlt">phase</span> chromatography and liquid chromatography in the critical condition. Chapter II decribes our study on the isocratic <span class="hlt">separation</span> of oligolysine (dp = 2 to 8) using a fixed content of acetonitrile (ACN) (23%) and different concentrations of HFBA in the mobile <span class="hlt">phase</span> (0.6-30.6 mM) on a Waters XBridge Shield RP18® column. We found that the retention time of oligolysine increases as the dp increases, because of an increased number of HFBA bound to the peptides. Furthermore, when [HFBA] increased, the retention time increased at different rates. The greater the dp, the faster the rate. Based on a closed pairing model that presumes an equilibrium between an unpaired state and the paired state with a fixed number of HFBA molecules, an equation was derived for the retention factor of oligolysine. In Chapter III, we compare retention behaviors of oligolysine (dp = 2 to 8) and oligoarginine (dp = 2 to 8) when they are <span class="hlt">separated</span> on the Waters XBridge Shield RP18® using fixed a ACN content (23%) and difference concentrations of HFBA (0.4-30.6 mM) in the mobile <span class="hlt">phase</span>. The retention time of oligoarginine also increased at different rates as [HFBA] increased. The greater the dp, the faster the rate. The retention time of oligolysine is shorter than that of oligarginine having the dame dp. We applied Eq.1 to analyze the plot of ln k as a function of [HFBA] for each oligopeptide component to obtain the values for n, Kip,m, and βKd,ip. For oligolysine, n increases linearly as dp increase and oligoarginine exhibits an accelerated increase in n as dp rises. The plot of ln βKd,ip against dp followed a linear relationship for both peptides. In Chapter IV, we study the effect of mobile <span class="hlt">phase</span> composition on the retention of oligolysine (dp = 2 to 8) on the Waters XBridge Shield RP18 ®. The ACN content was changed from 20% to 33% and the HFBA concentration from 0.7 to</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26651704','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26651704"><span>Molecular dynamics study of <span class="hlt">phase</span> <span class="hlt">separation</span> in fluids with chemical reactions.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Krishnan, Raishma; Puri, Sanjay</p> <p>2015-11-01</p> <p>We present results from the first d=3 molecular dynamics (MD) study of <span class="hlt">phase-separating</span> fluid mixtures (AB) with simple chemical reactions (A⇌B). We focus on the case where the rates of forward and backward reactions are equal. The chemical reactions compete with segregation, and the coarsening system settles into a steady-state mesoscale morphology. However, hydrodynamic effects destroy the lamellar morphology which characterizes the diffusive case. This has important consequences for the <span class="hlt">phase-separating</span> structure, which we study in detail. In particular, the equilibrium length scale (ℓ(eq)) in the steady state suggests a power-law dependence on the reaction rate ε:ℓ(eq)∼ε(-θ) with θ≃1.0.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004JaJAP..43.1578M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004JaJAP..43.1578M"><span>Polymer Wall Formation Using Liquid-Crystal/Polymer <span class="hlt">Phase</span> <span class="hlt">Separation</span> Induced on Patterned Polyimide Films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Murashige, Takeshi; Fujikake, Hideo; Sato, Hiroto; Kikuchi, Hiroshi; Kurita, Taiichiro; Sato, Fumio</p> <p>2004-12-01</p> <p>We could form lattice-shaped polymer walls in a liquid crystal (LC) layer through the thermal <span class="hlt">phase</span> <span class="hlt">separation</span> of an LC/polystyrene solution between substrates with polyimide films etched by short-wavelength ultraviolet irradiation using a photomask. The LC wetting difference between the polyimide and substrate surfaces caused the coalescence of growing LC droplets on patterned polyimide films with the progress of <span class="hlt">phase</span> <span class="hlt">separation</span>. Consequently, polymer walls were formed on substrate surface areas without polyimide films. The shape of the polymer wall formed became sharp with the use of rubbed polyimide films because the nucleation of growing LC droplets concentrated on the patterned polyimide films. It is thought that the increase in the alignment order of LC molecules in the solution near the rubbed polyimide films promotes the formation of LC molecular aggregation, which becomes the growth nuclei of LC droplets.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4792294','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4792294"><span>Tunable tissue scaffolds fabricated by in situ crosslink in <span class="hlt">phase</span> <span class="hlt">separation</span> system</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Liu, Xifeng; Chen, Wenjian; Gustafson, Carl T.; Miller, A. Lee; Waletzki, Brian E.; Yaszemski, Michael J.; Lu, Lichun</p> <p>2015-01-01</p> <p>Three-dimensional (3-D) scaffolds with intrinsic porous structures are desirable in various tissue regeneration applications. In this study, a unique method that combines thermally induced <span class="hlt">phase</span> <span class="hlt">separation</span> with a photocrosslinking process was developed for the fabrication of 3-D crosslinked polymer scaffolds with densely interconnected porous structures. Biodegradable poly(propylene fumarate)-co-poly(L-lactic acid) with crosslinkable fumarate bonds were used as the structural polymer material and a dioxane/water binary system was applied for the <span class="hlt">phase</span> <span class="hlt">separation</span>. By altering the polymer composition (9, 5 and 3 wt%), different types of scaffolds with distinct morphology, mechanical strength, degradation rate, cell growth and morphology, and extracellular matrix production were fabricated. These crosslinked 3-D porous scaffolds with tunable strength and biological responses show promise for potential applications in regenerative therapies, including bone and neural tissue engineering. PMID:26989479</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016NatSR...632727T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016NatSR...632727T"><span>Synthesis of semicrystalline nanocapsular structures obtained by Thermally Induced <span class="hlt">Phase</span> <span class="hlt">Separation</span> in nanoconfinement</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Torino, Enza; Aruta, Rosaria; Sibillano, Teresa; Giannini, Cinzia; Netti, Paolo A.</p> <p>2016-09-01</p> <p><span class="hlt">Phase</span> <span class="hlt">separation</span> of a polymer solution exhibits a peculiar behavior when induced in a nanoconfinement. The energetic constraints introduce additional interactions between the polymer segments that reduce the number of available configurations. In our work, this effect is exploited in a one-step strategy called nanoconfined-Thermally Induced <span class="hlt">Phase</span> <span class="hlt">Separation</span> (nc-TIPS) to promote the crystallization of polymer chains into nanocapsular structures of controlled size and shell thickness. This is accomplished by performing a quench step of a low-concentrated PLLA-dioxane-water solution included in emulsions of mean droplet size <500 nm acting as nanodomains. The control of nanoconfinement conditions enables not only the production of nanocapsules with a minimum mean particle diameter of 70 nm but also the tunability of shell thickness and its crystallinity degree. The specific properties of the developed nanocapsular architectures have important implications on release mechanism and loading capability of hydrophilic and lipophilic payload compounds.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004JChPh.120.9330L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004JChPh.120.9330L"><span>A Langevin dynamics study of mobile filler particles in <span class="hlt">phase-separating</span> binary systems</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Laradji, Mohamed</p> <p>2004-05-01</p> <p>The dynamics of <span class="hlt">phase</span> <span class="hlt">separation</span> in a simple binary mixture containing mobile filler particles that are preferentially wet by one of the two components is investigated systematically via Langevin simulations in two dimensions. We found that while the filler particles reduce the growth rate of spinodal decomposition, the domain growth remains essentially identical to that of the pure binary mixture. The growth rate diminishes as either the filler particles concentration is increased or their diffusivity is decreased.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19488170','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19488170"><span><span class="hlt">Phase</span> space tomography reconstruction of the Wigner distribution for optical beams <span class="hlt">separable</span> in Cartesian coordinates.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cámara, Alejandro; Alieva, Tatiana; Rodrigo, José A; Calvo, María L</p> <p>2009-06-01</p> <p>We propose a simple approach for the <span class="hlt">phase</span> space tomography reconstruction of the Wigner distribution of paraxial optical beams <span class="hlt">separable</span> in Cartesian coordinates. It is based on the measurements of the antisymmetric fractional Fourier transform power spectra, which can be taken using a flexible optical setup consisting of four cylindrical lenses. The numerical simulations and the experimental results clearly demonstrate the feasibility of the proposed scheme.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007PhRvB..75g3401L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007PhRvB..75g3401L"><span>Fluctuations and patterns in nanoscale surface reaction systems: Influence of reactant <span class="hlt">phase</span> <span class="hlt">separation</span> during CO oxidation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liu, Da-Jiang; Evans, J. W.</p> <p>2007-02-01</p> <p>A realistic atomistic model is used to assess spatiotemporal behavior in nanoscale CO oxidation systems at higher pressures than for traditional ultrahigh vacuum studies. The strong influence of adspecies interactions in this regime of high reactant coverages leads to <span class="hlt">phase</span> <span class="hlt">separation</span> between oxygen-rich and CO-rich reactive states. Time-series studies reveal fluctuation-induced transitions between these states, as well as transitions between reactive and inactive states. In addition, we observe flickering spatial patterns with sharp boundaries.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24123636','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24123636"><span>In situ studies of <span class="hlt">phase</span> <span class="hlt">separation</span> and crystallization directed by Marangoni instabilities during spin-coating.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Toolan, Daniel T W; Pullan, Nikki; Harvey, Michael J; Topham, Paul D; Howse, Jonathan R</p> <p>2013-12-23</p> <p>Results of a pioneering study are presented in which for the first time, crystallization, <span class="hlt">phase</span> <span class="hlt">separation</span> and Marangoni instabilities occurring during the spin-coating of polymer blends are directly visualized, in real-space and real-time. The results provide exciting new insights into the process of self-assembly, taking place during spin-coating, paving the way for the rational design of processing conditions, to allow desired morphologies to be obtained.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23182277','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23182277"><span>Utilization of a diol-stationary <span class="hlt">phase</span> column in ion chromatographic <span class="hlt">separation</span> of inorganic anions.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Arai, Kaori; Mori, Masanobu; Kozaki, Daisuke; Nakatani, Nobutake; Itabashi, Hideyuki; Tanaka, Kazuhiko</p> <p>2012-12-28</p> <p>We describe the ion chromatographic <span class="hlt">separation</span> of inorganic anions using a diol-stationary <span class="hlt">phase</span> column (-CH(OH)CH(2)OH; diol-column) without charged functional groups. Anions were <span class="hlt">separated</span> using acidic eluent as in typical anion-exchange chromatography. The retention volumes of anions on the diol-column increased with increasing H(+) concentration in the eluent. The anion-exchange capacities of diol-columns in the acidic eluent (pH 2.8) were larger than that of zwitterionic stationary <span class="hlt">phase</span> column but smaller than that of an anion-exchange column. The <span class="hlt">separation</span> of anions using the diol-column was strongly affected by the interaction of H(+) ions with the diol-functional groups and by the types of the eluents. In particular, the selection of the eluent was very important for controlling the retention time and resolution. Good <span class="hlt">separation</span> was obtained using a diol-column (HILIC-10) with 5 mM phthalic acid as eluent. The limits of detection at a signal-to-noise ratio of 3 ranged from 1.2 to 2.7 μM with relative standard deviations (RSD, n=5) of 0.04-0.07% for the retention time and 0.4-2.0% for the peak areas. This method was successfully applied to the determination of H(2)PO(4)(-), Cl(-), and NO(3)(-) in a liquid fertilizer sample.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22365122','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22365122"><span>Hydrophobic polymer monoliths as novel <span class="hlt">phase</span> <span class="hlt">separators</span>: application in continuous liquid-liquid extraction systems.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Peroni, Daniela; Vanhoutte, Dominique; Vilaplana, Francisco; Schoenmakers, Peter; de Koning, Sjaak; Janssen, Hans-Gerd</p> <p>2012-03-30</p> <p>Hydrophobic macroporous polymer monoliths are shown to be interesting materials for the construction of "selective solvent gates". With the appropriate surface chemistry and porous properties the monoliths can be made permeable only for apolar organic solvents and not for water. Different poly(butyl methacrylate-co-ethylene dimethacrylate) (BMA-EDMA) and poly(styrene-co-divinylbenzene) (PS-DVB) monoliths prepared with tailored chemistries and porosities were evaluated for this purpose. After extensive characterization, the PS-DVB monoliths were selected due to their higher hydrophobicity and their more suitable flow characteristics. BMA-EDMA monoliths are preferred for mid-polarity solvents such as ethyl acetate, for which they provide efficient <span class="hlt">separation</span> from water. Breakthrough experiments confirmed that the pressures necessary to generate flow of organic solvents through PS-DVB monoliths were substantially lower than for water. A <span class="hlt">phase</span> <span class="hlt">separator</span> was constructed using the monoliths as the flow selector. This device was successfully coupled on-line with a chip-based continuous liquid-liquid-extraction (LLE) system with segmented flow. Efficient <span class="hlt">separation</span> of different solvents was obtained across a wide range of flow rates (0.5-4.0 mL min(-1)) and aqueous-to-organic flow ratios (β=1-10). Good robustness and long life-time were also confirmed. The suitability of the device to perform simple, cheap, and reliable <span class="hlt">phase</span> <span class="hlt">separation</span> in a continuous LLE system prior to gas-chromatographic analysis was proven for some selected real-life applications.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23818579','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23818579"><span><span class="hlt">Phase</span> <span class="hlt">separation</span> explains a new class of self-organized spatial patterns in ecological systems.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Quan-Xing; Doelman, Arjen; Rottschäfer, Vivi; de Jager, Monique; Herman, Peter M J; Rietkerk, Max; van de Koppel, Johan</p> <p>2013-07-16</p> <p>The origin of regular spatial patterns in ecological systems has long fascinated researchers. Turing's activator-inhibitor principle is considered the central paradigm to explain such patterns. According to this principle, local activation combined with long-range inhibition of growth and survival is an essential prerequisite for pattern formation. Here, we show that the physical principle of <span class="hlt">phase</span> <span class="hlt">separation</span>, solely based on density-dependent movement by organisms, represents an alternative class of self-organized pattern formation in ecology. Using experiments with self-organizing mussel beds, we derive an empirical relation between the speed of animal movement and local animal density. By incorporating this relation in a partial differential equation, we demonstrate that this model corresponds mathematically to the well-known Cahn-Hilliard equation for <span class="hlt">phase</span> <span class="hlt">separation</span> in physics. Finally, we show that the predicted patterns match those found both in field observations and in our experiments. Our results reveal a principle for ecological self-organization, where <span class="hlt">phase</span> <span class="hlt">separation</span> rather than activation and inhibition processes drives spatial pattern formation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015APS..MARF43002R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015APS..MARF43002R"><span>Controlling <span class="hlt">Phase</span> <span class="hlt">Separation</span> of Interpenetrating Polymer Networks by Addition of Block Copolymers</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rohde, Brian; Krishnamoorti, Ramanan; Robertson, Megan</p> <p>2015-03-01</p> <p>Interpenetrating polymer networks (IPNs) offer a unique way to produce mechanically superior thermoset blends relative to the neat components. In this study, IPNs were prepared consisting of polydicyclopentadiene (polyDCPD), contributing high fracture toughness, and an epoxy resin (the diglycidyl ether of bisphenol A cured with nadic methyl anhydride), contributing high tensile strength and modulus. In the absence of compatibilization, the simultaneous curing of the networks leads to a macroscopically <span class="hlt">phase</span> <span class="hlt">separated</span> blend that exhibits poor mechanical behavior. To control <span class="hlt">phase</span> <span class="hlt">separation</span> and drive the system towards more mechanically robust nanostructured IPNs, block copolymers were designed to compatibilize this system, where one block possesses affinity to polyDCPD (polynorbornene in this study) and the other block possesses affinity to DGEBA (poly(ɛ-caprolactone) in this study). The influence of the block copolymer composition on the degree of <span class="hlt">phase</span> <span class="hlt">separation</span> and interfacial adhesion in the IPN was studied using a combination of small-angle scattering and imaging techniques. The resultant mechanical properties were explored and structure-property relationships were developed in this blend system.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014MolPh.112.1313R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014MolPh.112.1313R"><span>Salt-induced effective interactions and <span class="hlt">phase</span> <span class="hlt">separation</span> of an ultrasoft model of polyelectrolytes</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rotenberg, Benjamin; Bernard, Olivier; Hansen, Jean-Pierre</p> <p>2014-05-01</p> <p>We use a semi-grand canonical version of mean-field density functional theory to determine the total effective interaction energy of a solution of penetrable polyions characterised by a Gaussian charge distribution, in the presence of added salt. We then apply this effective representation of semi-flexible polyelectrolyte chains to investigate the possibility of a <span class="hlt">phase</span> <span class="hlt">separation</span> similar to that predicted earlier for charge-stabilised hard-sphere colloids. Apart from the absence of a hard-core repulsion, the effective pair potential is similar to the familiar Derjaguin-Landau-Verwey-Overbeek (DLVO) potential between charged-stabilised colloids, i.e. of the screened-Coulomb (Yukawa) form, but the effective valence of the polyions differs significantly from that of the DLVO pair potential, especially at high salt concentration. The existence of a well-defined closed-loop spinodal curve predicted by our mean-field calculation points to a <span class="hlt">phase</span> <span class="hlt">separation</span> between solutions with high and low polyion concentrations under reasonable physical conditions. The salt concentration at the upper critical point is typically two orders of magnitude larger than in the case of hard-core polyions, indicating that polyion penetrability appears to enhance the tendency towards <span class="hlt">phase</span> <span class="hlt">separation</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5041185','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5041185"><span>Correlation between structural heterogeneity and plastic deformation for <span class="hlt">phase</span> <span class="hlt">separating</span> FeCu metallic glasses</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Peng, Chuan-Xiao; Song, Kai-Kai; Wang, Li; Şopu, Daniel; Pauly, Simon; Eckert, Jürgen</p> <p>2016-01-01</p> <p>Unlike crystalline metals, the plastic deformation of metallic glasses (MGs) involves a competition between disordering and structural relaxation ordering, which is not well understood, yet. Molecular dynamics (MD) simulations were performed to investigate the evolutions of strain localizations, short-range order (SRO) as well as the free volume in the glass during compressive deformation of Fe50Cu50 MGs with different degrees of <span class="hlt">phase</span> <span class="hlt">separation</span>. Our findings indicate that the free volume in the <span class="hlt">phase</span> <span class="hlt">separating</span> MGs decreases while the shear strain localizations increase with increasing degree of <span class="hlt">phase</span> <span class="hlt">separation</span>. Cu-centered clusters show higher potential energies and Voronoi volumes, and bear larger local shear strains. On the other hand, Fe-centered pentagon-rich clusters in Cu-rich regions seem to play an important role to resist the shear transformation. The dilatation or annihilation of Voronoi volumes is due to the competition between ordering via structural relaxation and shear stress-induced deformation. The present study could provide a better understanding of the relationship between the structural inhomogeneity and the deformation of MGs. PMID:27681052</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26478268','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26478268"><span>Unique insight into <span class="hlt">phase</span> <span class="hlt">separation</span> in polymer solar cells from their electric characteristics.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Jian; Zhang, Fujun; An, Qiaoshi; Sun, Qianqian; Zhang, Jian; Hu, Bin</p> <p>2015-11-28</p> <p>A series of polymer solar cells (PSCs) were fabricated with indene-C60 bisadduct (ICBA) or [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) as an electron acceptor and with PBDT-TS1 as an electron donor. The donor/acceptor (D/A) <span class="hlt">phase</span> <span class="hlt">separation</span> was adjusted with different solution processing methods, consisting of cool (room temperature, 20 °C) solution, hot (70 °C) solution and the solutions with solvent additive 1,8-diiodideoctane (DIO). The champion PCE of PSCs with ICBA or PC61BM as an electron acceptor is 4.32% or 5.97% for the active layers prepared from hot solution with DIO additive or cool solution with DIO additive, respectively. The improved PCEs should be attributed to the optimized D/A <span class="hlt">phase</span> <span class="hlt">separation</span> in the active layers by adjusting the redistribution of PC61BM or the ICBA among the PBDT-TS1 networks. The degree of <span class="hlt">phase</span> <span class="hlt">separation</span> of the active layers with different acceptors was evaluated according to the current density-voltage (J-V) curves of hole-only and electron-only devices. The distribution of PC61BM or ICBA molecules in the normal direction can be simply judged from the symmetry degree of J-V curves of electron-only devices measured under the forward and reverse bias.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21370827','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21370827"><span>Influence of film thickness on the <span class="hlt">phase</span> <span class="hlt">separation</span> mechanism in ultrathin conducting polymer blend films.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Meier, Robert; Ruderer, Matthias A; Diethert, Alexander; Kaune, Gunar; Körstgens, Volker; Roth, Stephan V; Müller-Buschbaum, Peter</p> <p>2011-03-31</p> <p>The film morphology of thin polymer blend films based on poly[(1-methoxy)-4-(2-ethylhexyloxy)-p-phenylenevinylene] (MEH-PPV) and poly(N-vinylcarbazole) (PVK) is probed as a function of film thickness. Blend films are prepared with spin-coating of polymer solutions with different concentrations on top of solid supports. The blending ratio of both conducting polymers is kept constant. The film and surface morphology is probed with grazing incidence ultrasmall-angle X-ray scattering (GIUSAXS) and atomic force microscopy (AFM). A linear dependence between the film thickness and the averaged <span class="hlt">phase</span> <span class="hlt">separation</span> is found. In addition, X-ray reflectivity measurements show an enrichment of PVK at the substrate interface. UV/vis spectroscopy measurements indicate a linearly increasing amount of both homopolymers in the blend films for increasing film thicknesses. The generalized knowledge about the influence of the film thickness on the <span class="hlt">phase</span> <span class="hlt">separation</span> behavior in conducting polymer blend films is finally used to describe the <span class="hlt">phase</span> <span class="hlt">separation</span> formation during the spin-coating process, and the results are discussed in the framework of an adapted Flory-Huggins theory for rodlike polymers.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_20 --> <div id="page_21" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="401"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016APS..MARY38006R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016APS..MARY38006R"><span>Controlling <span class="hlt">Phase</span> <span class="hlt">Separation</span> of Tough Interpenetrating Polymer Networks via Addition of Amphiphilic Block Copolymers</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rohde, Brian; Krishnamoorti, Ramanan; Robertson, Megan</p> <p></p> <p>Interpenetrating polymer networks (IPNs) offer a unique way to combine the mechanical properties of two thermoset systems. Often used to create a material that possesses both high toughness and tensile properties, here we use polydicyclopentadiene, cured via ring opening metathesis polymerization, to contribute high toughness and diglycidyl ether of bisphenol A cured via anhydride chemistry to contribute high tensile strength and modulus. As the uncompatibilized system reacts in the presence of one another, mesoscopic <span class="hlt">phase</span> <span class="hlt">separation</span> occurs and dictates the overall efficacy of combining mechanical properties. To control <span class="hlt">phase</span> <span class="hlt">separation</span> and drive the system towards more mechanically robust nanostructed IPNs, amphiphilic block copolymers of polybutadiene- b-polyethylene oxide, where one block possesses strong affinity to polyDCPD and the other the DGEBA, were added to the system. Here we present a systematic study of the influence of block copolymer composition in the overall blend on degree of <span class="hlt">phase</span> <span class="hlt">separation</span> and morphology using a combination of small-angle x-ray scattering (SAXS) and scanning electron microscopy (SEM) techniques. The resultant mechanical properties are then explored in an effort to link mechanical properties to blend morphology.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24666206','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24666206"><span>From molecular dehydration to excess volumes of <span class="hlt">phase-separating</span> PNIPAM solutions.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Philipp, Martine; Kyriakos, Konstantinos; Silvi, Luca; Lohstroh, Wiebke; Petry, Winfried; Krüger, Jan K; Papadakis, Christine M; Müller-Buschbaum, Peter</p> <p>2014-04-17</p> <p>For aqueous poly(N-isopropyl acrylamide) (PNIPAM) solutions, a structural instability leads to the collapse and aggregation of the macromolecules at the temperature-induced demixing transition. The accompanying cooperative dehydration of the PNIPAM chains is known to play a crucial role in this <span class="hlt">phase</span> <span class="hlt">separation</span>. We elucidate the impact of partial dehydration of PNIPAM on the volume changes related to the <span class="hlt">phase</span> <span class="hlt">separation</span> of dilute to concentrated PNIPAM solutions. Quasi-elastic neutron scattering enables us to directly follow the isotropic jump diffusion behavior of the hydration water and the almost freely diffusing water. As the hydration number decreases from 8 to 2 for the demixing 25 mass % PNIPAM solution, only a partial dehydration of the PNIPAM chains occurs. Dilatation studies reveal that the transition-induced volume changes depend in a remarkable manner on the PNIPAM concentration of the solutions. The excess volume per mole of H2O molecules expelled from the solvation layers of PNIPAM during <span class="hlt">phase</span> <span class="hlt">separation</span> probably strongly increases from dilute to concentrated PNIPAM solutions. This finding is qualitatively related to the immense strain-softening previously observed for demixing PNIPAM solutions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26572324','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26572324"><span>Lamellar, micro-<span class="hlt">phase</span> <span class="hlt">separated</span> blends of methyl cellulose and dendritic polyethylene glycol, POSS-PEG.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chinnam, Parameswara Rao; Mantravadi, Ramya; Jimenez, Jayvic C; Dikin, Dmitriy A; Wunder, Stephanie L</p> <p>2016-01-20</p> <p>Blends of methyl cellulose (MC) and liquid pegylated polyoctahedralsilsesquioxane (POSS-PEG) were prepared from non-gelled, aqueous solutions at room temperature (RT), which was below their gel temperatures (Tm). Lamellar, fibrillated films (pure MC) and increasingly micro-porous morphologies with increasing POSS-PEG content were formed, which had RT moduli between 1 and 5GPa. Evidence of distinct micro-<span class="hlt">phase</span> <span class="hlt">separated</span> MC and POSS-PEG domains was indicated by the persistence of the MC and POSS-PEG (at 77K) crystal structures in the X-ray diffraction data, and scanning transmission electron images. Mixing of MC and POSS-PEG in the interface region was indicated by suppression of crystallinity in the POSS-PEG, and increases/decreases in the glass transition temperatures (Tg) of POSS-PEG/MC in the blends compared with the pure components. These interface interactions may serve as cross-link sites between the micro-<span class="hlt">phase</span> <span class="hlt">separated</span> domains that permit incorporation of high amounts of POSS-PEG in the blends, prevent macro-<span class="hlt">phase</span> <span class="hlt">separation</span> and result in rubbery material properties (at high POSS-PEG content). Above Tg/Tm of POSS-PEG, the moduli of the blends increase with MC content as expected. However, below Tg/Tm of POSS-PEG, the moduli are greater for blends with high POSS-PEG content, suggesting that it behaves like semi-crystalline polyethylene oxide reinforced with silica (SiO1.5).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012APS..MART28012S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012APS..MART28012S"><span>Laser <span class="hlt">Phase</span> <span class="hlt">Separation</span> of Si Rich Oxides: The Role of Composition</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sungur Ozen, Emel; Aydinli, Atilla; Gundogdu, Sinan</p> <p>2012-02-01</p> <p>Continuous-wave laser annealing of Si-rich oxide thin films with varying Si content were performed in order to obtain Si nanocrystals (Sinc) embedded in silica. The composition, irradiation times and power densities were investigated as well as the role of hydrogen in <span class="hlt">phase</span> <span class="hlt">separation</span>. Sinc in SiO2 appear to be very promising for the realization of optical function as light emission or optical memory. Nanocrystaline Si finds also important utility in photovoltaics thanks to quantum confinement in the nanostructures offering a wider bandgap material which, in a tandem configuration, can allow a better use of the solar spectrum. Conventional techniques utilize high-temperature processing to obtain Si-SiO2 <span class="hlt">phase</span> <span class="hlt">separation</span>. These processes are not compatible with mass production methods. An alternative approach capable of avoiding high temperature processing is the laser annealing of SiOx films. The structural effect due to annealing were investigated by Raman and photoluminescence spectroscopy. It has been shown that the size and amount of Sinc depends both on the oxygen content and on the laser power density. PECVD grown hydrogenated SiOx films were compared with sputtered films without hydrogen to identify its role for the <span class="hlt">phase</span> <span class="hlt">separation</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25541813','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25541813"><span>Glass-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> in highly supersaturated aqueous solutions of telaprevir.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mosquera-Giraldo, Laura I; Taylor, Lynne S</p> <p>2015-02-02</p> <p>Amorphous solid dispersions are of great current interest because they can improve the delivery of poorly water-soluble compounds. It has been recently noted that the highly supersaturated solutions generated by dissolution of some ASDs can undergo a <span class="hlt">phase</span> transition to a colloidal, disordered, drug-rich <span class="hlt">phase</span> when the concentration exceeds the "amorphous solubility" of the drug. The purpose of this study was to investigate the <span class="hlt">phase</span> behavior of supersaturated solutions of telaprevir, which is formulated as an amorphous solid dispersion in the commercial product. Different analytical techniques including proton nuclear magnetic resonance spectroscopy (NMR), ultraviolet spectroscopy (UV), fluorescence spectroscopy and flux measurements were used to evaluate the properties of aqueous supersaturated solutions of telaprevir. It was found that highly supersaturated solutions of telaprevir underwent glass-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> (GLPS) when the concentration exceeded 90 μg/mL, forming a water-saturated colloidal, amorphous drug-rich <span class="hlt">phase</span> with a glass transition temperature of 52 °C. From flux measurements, it was observed that the "free" drug concentration reached a maximum at the concentration where GLPS occurred, and did not increase further as the concentration was increased. This <span class="hlt">phase</span> behavior, which results in a precipitate and a metastable equilibrium between a supersaturated solution and a drug-rich <span class="hlt">phase</span>, is obviously important in the context of evaluating amorphous solid dispersion formulations and their crystallization routes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17361308','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17361308"><span>X-ray <span class="hlt">phase</span>-contrast imaging: transmission functions <span class="hlt">separable</span> in Cartesian coordinates.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cao, Guohua; Hamilton, Theron J; Rose-Petruck, Christoph; Diebold, Gerald J</p> <p>2007-04-01</p> <p>In-line, x-ray <span class="hlt">phase</span>-contrast imaging is responsive to both <span class="hlt">phase</span> changes and absorption as the x radiation traverses a body. Expressions are derived for <span class="hlt">phase</span>-contrast imaging of objects having transmission functions <span class="hlt">separable</span> in Cartesian coordinates. Starting from the Fresnel-Kirchhoff integral formula for image formation, an expression is found for the <span class="hlt">phase</span>-contrast image produced by an x-ray source with nonvanishing dimensions. This expression is evaluated in limiting cases where the source-to-object distance is large, where the source acts as a point source, and where the weak <span class="hlt">phase</span> approximation is valid. The integral expression for the image is evaluated for objects with simple geometrical shapes, showing the influence of the source dimensions on the visibility of <span class="hlt">phase</span>-contrast features. The expressions derived here are evaluated for cases where the magnification is substantially greater than one as would be employed in biological imaging. Experiments are reported using the in-line <span class="hlt">phase</span>-contrast imaging method with a microfocus x-ray source and a CCD camera.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/2211900','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/2211900"><span><span class="hlt">Separation</span> and indirect detection of small-chain peptides using chromophoric mobile <span class="hlt">phase</span> additives.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yuan, D X; Pietrzyk, D J</p> <p>1990-06-22</p> <p>Ruthenium(II) 1,10-phenanthroline, Ru(phen)3(2+), and ruthenium(II) 2,2'-bipyridyl, Ru(bipy)3(2+), salts were evaluated as mobile <span class="hlt">phase</span> additives for the liquid chromatographic <span class="hlt">separation</span> of small-chain peptides on a polystyrene-divinylbenzene copolymeric (Hamilton PRP-1) stationary <span class="hlt">phase</span>. In a basic mobile <span class="hlt">phase</span> peptides are anions, and retention, resolution and detection occur because of the interactions between the stationary <span class="hlt">phase</span>, the RuII complex and the peptide anion. Since the RuII complex concentration changes in the analyte band relative to the background eluent RuII complex concentration, the peptide can be detected by indirect photometric detection using the wavelength where the RuII complex absorbs. Peptide analyte peaks may be positive or negative depending on the counter-anion and its concentration. Small-chain peptides that do not contain chromophoric side-chains are detected without derivatization at about 0.1 nmol injected at a 3:1 signal-to-noise ratio. Factors that affect retention, resolution and indirect photometric detection are the RuII complex, its mobile <span class="hlt">phase</span> concentration, mobile <span class="hlt">phase</span> pH and solvent composition, and the type and concentration of the mobile <span class="hlt">phase</span> counter-anion and/or buffer anion.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20010004305','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20010004305"><span><span class="hlt">Phase</span> <span class="hlt">Separation</span> Kinetics in Isopycnic Mixtures of H2O/CO2/Ethoxylated Alcohol Surfactants</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Lesemann, Markus; Paulaitis, Michael E.; Kaler, Eric W.</p> <p>1999-01-01</p> <p>Ternary mixtures of H2O and CO2 with ethoxylated alcohol (C(sub i)E(sub j)) surfactants form three coexisting liquid <span class="hlt">phases</span> at conditions where two of the <span class="hlt">phases</span> have equal densities (isopycnic <span class="hlt">phases</span>). Isopycnic <span class="hlt">phase</span> behavior has been observed for mixtures containing C8E5, C10E6, and C12E6 surfactants, but not for those mixtures containing either C4E1 or C8E3 surfactants. Pressure-temperature (PT) projections for this three-<span class="hlt">phase</span> equilibrium were determined for H2O/CO2/C8E5 and H2O/CO2/C10E6 mixtures at temperatures from approximately 25 to 33 C and pressures between 90 and 350 bar. Measurements of the microstructure in H2O/CO2/C12E6 mixtures as a function of temperature (25-31 C), pressure (63.1-90.7 bar), and CO2 composition (0-3.9 wt%) have also been carried out to show that while micellar structure remains essentially un-changed, critical concentration fluctuations increase as the <span class="hlt">phase</span> boundary and plait point are approached. In this report, we present our first measurements of the kinetics of isopycnic <span class="hlt">phase</span> <span class="hlt">separation</span> for ternary mixtures of H2O/CO2/C8E5.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1335132-dynamics-crowding-induced-mixing-phase-separated-lipid-bilayers','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1335132-dynamics-crowding-induced-mixing-phase-separated-lipid-bilayers"><span>Dynamics of crowding-induced mixing in <span class="hlt">phase</span> <span class="hlt">separated</span> lipid bilayers</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Zeno, Wade F.; Johnson, Kaitlin E.; Sasaki, Darryl Y.; ...</p> <p>2016-10-10</p> <p>We use fluorescence microscopy to examine the dynamics of the crowding-induced mixing transition of liquid ordered (Lo)–liquid disordered (Ld) <span class="hlt">phase</span> <span class="hlt">separated</span> lipid bilayers when the following particles of increasing size bind to either the Lo or Ld <span class="hlt">phase</span>: Ubiquitin, green fluorescent protein (GFP), and nanolipoprotein particles (NLPs) of two diameters. These proteinaceous particles contained histidine-tags, which were <span class="hlt">phase</span> targeted by binding to iminodiacetic acid (IDA) head groups, via a Cu2+ chelating mechanism, of lipids that specifically partition into either the Lo <span class="hlt">phase</span> or Ld <span class="hlt">phase</span>. The degree of steric pressure was controlled by varying the size of the bound particlemore » (10–240 kDa) and the amount of binding sites present (i.e., DPIDA concentrations of 9 and 12 mol%) in the supported lipid multibilayer platform used here. We develop a mass transfer-based diffusional model to analyze the observed Lo <span class="hlt">phase</span> domain dissolution that, along with visual observations and activation energy calculations, provides insight into the sequence of events in crowding-induced mixing. Furthermore, our results suggest that the degree of steric pressure and target <span class="hlt">phase</span> influence not only the efficacy of steric-pressure induced mixing, but the rate and controlling mechanism for which it occurs.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/1335132','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/1335132"><span>Dynamics of crowding-induced mixing in <span class="hlt">phase</span> <span class="hlt">separated</span> lipid bilayers</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Zeno, Wade F.; Johnson, Kaitlin E.; Sasaki, Darryl Y.; Risbud, Subhash H.; Longo, Marjorie L.</p> <p>2016-10-10</p> <p>We use fluorescence microscopy to examine the dynamics of the crowding-induced mixing transition of liquid ordered (L<sub>o</sub>)–liquid disordered (L<sub>d</sub>) <span class="hlt">phase</span> <span class="hlt">separated</span> lipid bilayers when the following particles of increasing size bind to either the L<sub>o</sub> or L<sub>d</sub> <span class="hlt">phase</span>: Ubiquitin, green fluorescent protein (GFP), and nanolipoprotein particles (NLPs) of two diameters. These proteinaceous particles contained histidine-tags, which were <span class="hlt">phase</span> targeted by binding to iminodiacetic acid (IDA) head groups, via a Cu<sup>2+</sup> chelating mechanism, of lipids that specifically partition into either the Lo <span class="hlt">phase</span> or Ld <span class="hlt">phase</span>. The degree of steric pressure was controlled by varying the size of the bound particle (10–240 kDa) and the amount of binding sites present (i.e., DPIDA concentrations of 9 and 12 mol%) in the supported lipid multibilayer platform used here. We develop a mass transfer-based diffusional model to analyze the observed L<sub>o</sub> <span class="hlt">phase</span> domain dissolution that, along with visual observations and activation energy calculations, provides insight into the sequence of events in crowding-induced mixing. Furthermore, our results suggest that the degree of steric pressure and target <span class="hlt">phase</span> influence not only the efficacy of steric-pressure induced mixing, but the rate and controlling mechanism for which it occurs.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24919675','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24919675"><span>Tube radial distribution phenomenon with a two-<span class="hlt">phase</span> <span class="hlt">separation</span> solution of a fluorocarbon and hydrocarbon organic solvent mixture in a capillary tube and metal compounds <span class="hlt">separation</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kitaguchi, Koichi; Hanamura, Naoya; Murata, Masaharu; Hashimoto, Masahiko; Tsukagoshi, Kazuhiko</p> <p>2014-01-01</p> <p>A fluorocarbon and hydrocarbon organic solvent mixture is known as a temperature-induced <span class="hlt">phase-separation</span> solution. When a mixed solution of tetradecafluorohexane as a fluorocarbon organic solvent and hexane as a hydrocarbon organic solvent (e.g., 71:29 volume ratio) was delivered in a capillary tube that was controlled at 10°C, the tube radial distribution phenomenon (TRDP) of the solvents was clearly observed through fluorescence images of the dye, perylene, dissolved in the mixed solution. The homogeneous mixed solution (single <span class="hlt">phase</span>) changed to a heterogeneous solution (two <span class="hlt">phases</span>) with inner tetradecafluorohexane and outer hexane <span class="hlt">phases</span> in the tube under laminar flow conditions, generating the dynamic liquid-liquid interface. We also tried to apply TRDP to a <span class="hlt">separation</span> technique for metal compounds. A model analyte mixture, copper(II) and hematin, was <span class="hlt">separated</span> through the capillary tube, and detected with a chemiluminescence detector in this order within 4 min.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22729039','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22729039"><span>Evaluation of a hydrophilic ionic liquid as a salting-out <span class="hlt">phase</span> <span class="hlt">separation</span> agent to a water-tetrahydrofuran homogeneous system for aqueous biphasic extraction <span class="hlt">separation</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hirayama, Naoki; Higo, Takaaki; Imura, Hisanori</p> <p>2012-01-01</p> <p>The use of a hydrophilic ionic liquid (IL), 1-butyl-3-methylimidazolium chloride (C(4)mimCl), as a salting-out <span class="hlt">phase</span> <span class="hlt">separation</span> agent to a water-tetrahydrofuran homogeneous system was studied for possible applications to novel aqueous biphasic extraction <span class="hlt">separation</span>. The IL showed a salting-out <span class="hlt">phase-separation</span> ability. Also, differences in the polarity between the formed two <span class="hlt">phases</span> were smaller than that when using NaCl as a salting-out agent. This result suggested that C(4)mimCl remaining in water-rich <span class="hlt">phase</span> acts not only as a salting-out agent, but also a component of a mixed-solvent. Possible uses of C(4)mimCl/NaCl mixed salting-out agent system were also discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/22309044','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/22309044"><span><span class="hlt">Phase</span> <span class="hlt">separation</span> and antisite defects in the thermoelectric TiNiSn half-Heusler alloys</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Kirievsky, K.; Gelbstein, Y. Fuks, D.</p> <p>2013-07-15</p> <p>The half-Heusler TiNiSn alloys have recently gained an attention as promising candidates for thermoelectric applications. Improvement of these alloys for such applications can be obtained by both electronic and compositional optimizations. The latter can result in a miscibility gap, allowing a <span class="hlt">phase</span> <span class="hlt">separation</span> in the nano-scale and consequently a thermal conductivity reduction. Combination of ab initio calculations and statistical thermodynamics was applied for studying the relative stability of a number of superstructures in TiNiSn based alloys. The quasi-binary <span class="hlt">phase</span> diagram beyond T=0 K for TiNiSn–TiNi{sub 2}Sn solid solutions was calculated using energy parameters extracted from the total energy calculations for ordered structures in the Ni sublattice. We demonstrated that a decomposition of the off-stoichiometric Ni-rich half-Heusler alloy into the stoichiometric TiNiSn <span class="hlt">phase</span> and into Ni deficient Heusler TiNi{sub 2}Sn <span class="hlt">phase</span> occurs at elevated temperatures—an effect which recently had been observed experimentally. Furthermore, favorable energetic conditions for antisite defects formation were deduced, based on calculations of the energy of formation, an effect which was explained as a cooperative process of partial disordering on the Ni sublattice. The influence of these two effects on improvement of the thermoelectric performance of TiNiSn based half Heusler compounds is discussed. - Graphical abstract: <span class="hlt">Phase</span> <span class="hlt">separation</span> and antisite defects in the thermoelectric TiNiSn alloy, are covered as methods for nanostructuring and thereby enhancement of the thermoelectric potential. - Highlights: • Ab initio calculations/statistical thermodynamics was applied for studying the TiNiSn system. • The <span class="hlt">phase</span> diagram for TiNiSn–TiNi{sub 2}Sn solid solutions was calculated. • Decomposition of the Ni-rich HH into TiNiSn and Ni deficient TiNi{sub 2}Sn <span class="hlt">phases</span> was observed. • Favorable energetic conditions for antisite defects formation were deduced.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015PhDT.......113G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015PhDT.......113G"><span>Effect of electric field and strain on the magnetic properties of <span class="hlt">phase</span> <span class="hlt">separated</span> manganites</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Grant, Daniel M.</p> <p></p> <p>Perovskite manganese oxide (manganites) have attracted research attention due to a wide variety of complex behaviors observed, including colossal responses to external perturbations. More recent work has focused on the competing ground states and the coexistence of magnetic and non-magnetic <span class="hlt">phases</span> in manganites. Anisotropic resistance changes have been observed in high quality thin film manganites, possibly due to dielectrophoresis, upon application of an electric field. Dielectrophoresis is usually observed in fluid-like systems in an electric field but is surprisingly useful in explaining the transport properties of manganites due to the fluid-like behavior of competing <span class="hlt">phases</span>. A main goal of this dissertation is to explore the role of magnetic interactions on the dielectrophoresis effects on ferromagnetic metallic regions in <span class="hlt">phase</span> <span class="hlt">separated</span> manganite thin films. The combined effect of electric and magnetic fields in these manganites could reveal a novel form of magnetoelectric effect. In one set of experiments, a magnetic field decreased the amount of time needed for the dielectrophoresis to lead to a large drop in the resistance along one direction, showing the importance of magnetic interactions in dielectrophoresis. In another set of experiments, breaking down the large resistance of a manganite sample produced a small change in coercive field, further confirming the relationship between electric and magnetic effects in manganites. However, the largest effect on the magnetic properties of the thin films was from confinement of the competing <span class="hlt">phases</span> in micrometer scale structures fabricated on the thin films. Coercive field increases of about 100- 400% were observed in a certain range of film thicknesses. To analyze such behavior in manganites, high quality thin films of the <span class="hlt">phase-separated</span> manganite (La1-xPrx)1-yCa yMnO3 (LPCMO) were grown on NdGaO3 (NGO) substrates using pulsed laser deposition. Mangetotransport, magnetization, and scanning probe microscopy</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/6356523','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/6356523"><span><span class="hlt">Separation</span> of mycotoxins, polycyclic aromatic hydrocarbons, quinones, and heterocyclic compounds on cyclodextrin bonded <span class="hlt">phases</span>: an alternative LC packing</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Armstrong, D.W.; Alak, A.; De Mond, W.; Hinze, W.L.; Riehl, T.E.</p> <p>1985-01-01</p> <p>..beta..-Cyclodextrin and gamma-cyclodextrin chiral bonded <span class="hlt">phases</span> were previously shown to be useful in the <span class="hlt">separation</span> of enantiomers, diastereomers and structural isomers. In this work it is demonstrated that these stationary <span class="hlt">phases</span> are also useful in more routine <span class="hlt">separations</span>. As such, they provide an alternative to the popular reverse <span class="hlt">phase</span> packings. Because the selectivity of cyclodextrin packings is often unique they can be used to compliment conventional columns, particularly when <span class="hlt">separating</span> complex mixtures where peak overlap is a problem. The <span class="hlt">separation</span> of several important classes of compounds is used to demonstrate the general utility of this packing.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26636608','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26636608"><span>On-Chip Pressure Generation for Driving Liquid <span class="hlt">Phase</span> <span class="hlt">Separations</span> in Nanochannels.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Xia, Ling; Choi, Chiwoong; Kothekar, Shrinivas C; Dutta, Debashis</p> <p>2016-01-05</p> <p>In this Article, we describe the generation of pressure gradients on-chip for driving liquid <span class="hlt">phase</span> <span class="hlt">separations</span> in submicrometer deep channels. The reported pressure-generation capability was realized by applying an electrical voltage across the interface of two glass channel segments with different depths. A mismatch in the electroosmotic flow rate at this junction led to the generation of pressure-driven flow in our device, a fraction of which was then directed to an analysis channel to carry out the desired <span class="hlt">separation</span>. Experiments showed the reported strategy to be particularly conducive for miniaturization of pressure-driven <span class="hlt">separations</span> yielding flow velocities in the <span class="hlt">separation</span> channel that were nearly unaffected upon scaling down the depth of the entire fluidic network. Moreover, the small dead volume in our system allowed for high dynamic control over this pressure gradient, which otherwise was challenging to accomplish during the sample injection process using external pumps. Pressure-driven velocities up to 3.1 mm/s were realized in <span class="hlt">separation</span> ducts as shallow as 300 nm using our current design for a maximum applied voltage of 3 kV. The functionality of this integrated device was demonstrated by implementing a pressure-driven ion chromatographic analysis that relied on analyte interaction with the nanochannel surface charges to yield a nonuniform solute concentration across the channel depth. Upon coupling such analyte distribution to the parabolic pressure-driven flow profile in the <span class="hlt">separation</span> duct, a mixture of amino acids could be resolved. The reported assay yielded a higher <span class="hlt">separation</span> resolution compared to its electrically driven counterpart in which sample migration was realized using electroosmosis/electrophoresis.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2006JChPh.124e4503H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2006JChPh.124e4503H"><span>Pair-correlation functions and <span class="hlt">phase</span> <span class="hlt">separation</span> in a two-component point Yukawa fluid</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hopkins, P.; Archer, A. J.; Evans, R.</p> <p>2006-02-01</p> <p>We investigate the structure of a binary mixture of particles interacting via purely repulsive point Yukawa pair potentials with a common inverse screening length λ. Using the hypernetted chain closure to the Ornstein-Zernike equations, we find that for a system with "ideal" (Berthelot mixing rule) pair-potential parameters for the interaction between unlike species, the asymptotic decay of the total correlation functions crosses over from monotonic to damped oscillatory on increasing the fluid total density at fixed composition. This gives rise to a Kirkwood line in the <span class="hlt">phase</span> diagram. We also consider a "nonideal" system, in which the Berthelot mixing rule is multiplied by a factor (1+δ). For any δ >0 the system exhibits fluid-fluid <span class="hlt">phase</span> <span class="hlt">separation</span> and remarkably the ultimate decay of the correlation functions is now monotonic for all (mixture) state points. Only in the limit of vanishing concentration of either species does one find oscillatory decay extending to r =∞. In the nonideal case the simple random-<span class="hlt">phase</span> approximation provides a good description of the <span class="hlt">phase</span> <span class="hlt">separation</span> and the accompanying Lifshitz line.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017OptLT..89...75T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017OptLT..89...75T"><span>Carrier-<span class="hlt">separating</span> demodulation of <span class="hlt">phase</span> shifting self-mixing interferometry</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Tao, Yufeng; Wang, Ming; Xia, Wei</p> <p>2017-03-01</p> <p>A carrier <span class="hlt">separating</span> method associated with noise-elimination had been introduced into a sinusoidal <span class="hlt">phase</span>-shifting self-mixing interferometer. The conventional sinusoidal <span class="hlt">phase</span> shifting self-mixing interferometry was developed into a more competitive instrument with high computing efficiency and nanometer accuracy of λ / 100 in dynamical vibration measurement. The high slew rate electro-optic modulator induced a sinusoidal <span class="hlt">phase</span> carrier with ultralow insertion loss in this paper. In order to extract <span class="hlt">phase</span>-shift quickly and precisely, this paper employed the carrier-<span class="hlt">separating</span> to directly generate quadrature signals without complicated frequency domain transforms. Moreover, most noises were evaluated and suppressed by a noise-elimination technology synthesizing empirical mode decomposition with wavelet transform. The overall laser system was described and inherent advantages such as high computational efficiency and decreased nonlinear errors of the established system were demonstrated. The experiment implemented on a high precision PZT (positioning accuracy was better than 1 nm) and compared with laser Doppler velocity meter. The good agreement of two instruments shown that the short-term resolution had improved from 10 nm to 1.5 nm in dynamic vibration measurement with reduced time expense. This was useful in precision measurement to improve the SMI with same sampling rate. The proposed signal processing was performed in pure time-domain requiring no preprocessing electronic circuits.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28231012','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28231012"><span>Quantum Percolation and Magnetic Nanodroplet States in Electronically <span class="hlt">Phase-Separated</span> Manganite Nanowires.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Kaixuan; Li, Lin; Li, Hui; Feng, Qiyuan; Zhang, Nan; Cheng, Long; Fan, Xiaodong; Hou, Yubin; Lu, Qingyou; Zhang, Zhenyu; Zeng, Changgan</p> <p>2017-03-08</p> <p>One-dimensional (1D) confinement has been revealed to effectively tune the properties of materials in homogeneous states. The 1D physics can be further enriched by electronic inhomogeneity, which unfortunately remains largely unknown. Here we demonstrate the ultrahigh sensitivity to magnetic fluctuations and the tunability of <span class="hlt">phase</span> stability in the electronic transport properties of self-assembled electronically <span class="hlt">phase-separated</span> manganite nanowires with extreme aspect ratio. The onset of magnetic nanodroplet state, a precursor to the ferromagnetic metallic state, is unambiguously revealed, which is attributed to the small lateral size of the nanowires that is comparable to the droplet size. Moreover, the quasi-1D anisotropy stabilizes thin insulating domains to form intrinsic tunneling junctions in the low temperature range, which is robust even under magnetic field up to 14 T and thus essentially modifies the classic 1D percolation picture to stabilize a novel quantum percolation state. A new <span class="hlt">phase</span> diagram is therefore established for the manganite system under quasi-1D confinement for the first time. Our findings offer new insight into understanding and manipulating the colorful properties of the electronically <span class="hlt">phase-separated</span> systems via dimensionality engineering.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4561900','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4561900"><span>Pressure-induced electronic <span class="hlt">phase</span> <span class="hlt">separation</span> of magnetism and superconductivity in CrAs</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Khasanov, Rustem; Guguchia, Zurab; Eremin, Ilya; Luetkens, Hubertus; Amato, Alex; Biswas, Pabitra K.; Rüegg, Christian; Susner, Michael A.; Sefat, Athena S.; Zhigadlo, Nikolai D.; Morenzoni, Elvezio</p> <p>2015-01-01</p> <p>The recent discovery of pressure (p) induced superconductivity in the binary helimagnet CrAs has raised questions on how superconductivity emerges from the magnetic state and on the mechanism of the superconducting pairing. In the present work the suppression of magnetism and the occurrence of superconductivity in CrAs were studied by means of muon spin rotation. The magnetism remains bulk up to p  3.5 kbar while its volume fraction gradually decreases with increasing pressure until it vanishes at p  7 kbar. At 3.5 kbar superconductivity abruptly appears with its maximum Tc  1.2 K which decreases upon increasing the pressure. In the intermediate pressure region (3.5  p  7 kbar) the superconducting and the magnetic volume fractions are spatially <span class="hlt">phase</span> <span class="hlt">separated</span> and compete for <span class="hlt">phase</span> volume. Our results indicate that the less conductive magnetic <span class="hlt">phase</span> provides additional carriers (doping) to the superconducting parts of the CrAs sample thus leading to an increase of the transition temperature (Tc) and of the superfluid density (ρs). A scaling of ρs with as well as the <span class="hlt">phase</span> <span class="hlt">separation</span> between magnetism and superconductivity point to a conventional mechanism of the Cooper-pairing in CrAs. PMID:26346548</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_21 --> <div id="page_22" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="421"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26346548','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26346548"><span>Pressure-induced electronic <span class="hlt">phase</span> <span class="hlt">separation</span> of magnetism and superconductivity in CrAs.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Khasanov, Rustem; Guguchia, Zurab; Eremin, Ilya; Luetkens, Hubertus; Amato, Alex; Biswas, Pabitra K; Rüegg, Christian; Susner, Michael A; Sefat, Athena S; Zhigadlo, Nikolai D; Morenzoni, Elvezio</p> <p>2015-09-08</p> <p>The recent discovery of pressure (p) induced superconductivity in the binary helimagnet CrAs has raised questions on how superconductivity emerges from the magnetic state and on the mechanism of the superconducting pairing. In the present work the suppression of magnetism and the occurrence of superconductivity in CrAs were studied by means of muon spin rotation. The magnetism remains bulk up to p ≃ 3.5 kbar while its volume fraction gradually decreases with increasing pressure until it vanishes at p ≃ 7 kbar. At 3.5 kbar superconductivity abruptly appears with its maximum Tc ≃ 1.2 K which decreases upon increasing the pressure. In the intermediate pressure region (3.5 < or ~  p < or ~ 7 kbar) the superconducting and the magnetic volume fractions are spatially <span class="hlt">phase</span> <span class="hlt">separated</span> and compete for <span class="hlt">phase</span> volume. Our results indicate that the less conductive magnetic <span class="hlt">phase</span> provides additional carriers (doping) to the superconducting parts of the CrAs sample thus leading to an increase of the transition temperature (Tc) and of the superfluid density (ρs). A scaling of ρs with Tc(3.2) as well as the <span class="hlt">phase</span> <span class="hlt">separation</span> between magnetism and superconductivity point to a conventional mechanism of the Cooper-pairing in CrAs.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/servlets/purl/1259706','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/servlets/purl/1259706"><span>Pressure-induced electronic <span class="hlt">phase</span> <span class="hlt">separation</span> of magnetism and superconductivity in CrAs</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Khasanov, Rustem; Guguchia, Zurab; Eremin, Ilya; Luetkens, Hubertus; Amato, Alex; Biswas, Pabitra K.; Ruegg, Christian; Susner, Michael A.; Sefat, Athena S.; Zhigadlo, Nikolai D.; Morenzoni, Elvezio</p> <p>2015-09-08</p> <p>We report that the recent discovery of pressure (p) induced superconductivity in the binary helimagnet CrAs has raised questions on how superconductivity emerges from the magnetic state and on the mechanism of the superconducting pairing. In the present work the suppression of magnetism and the occurrence of superconductivity in CrAs were studied by means of muon spin rotation. The magnetism remains bulk up to p ≃ 3.5 kbar while its volume fraction gradually decreases with increasing pressure until it vanishes at p ≃ 7 kbar. At 3.5 kbar superconductivity abruptly appears with its maximum T<sub>c</sub> ≃ 1.2 K which decreases upon increasing the pressure. In the intermediate pressure region (3.5≲ p ≲ 7 kbar) the superconducting and the magnetic volume fractions are spatially <span class="hlt">phase</span> <span class="hlt">separated</span> and compete for <span class="hlt">phase</span> volume. Our results indicate that the less conductive magnetic <span class="hlt">phase</span> provides additional carriers (doping) to the superconducting parts of the CrAs sample thus leading to an increase of the transition temperature (T<sub>c</sub>) and of the superfluid density (ρ<sub>s</sub>). A scaling of ρ<sub>s</sub> with T<sub>c</sub><sup>3.2</sup> as well as the <span class="hlt">phase</span> <span class="hlt">separation</span> between magnetism and superconductivity point to a conventional mechanism of the Cooper-pairing in CrAs.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19950058801&hterms=design+management&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Ddesign%2Bmanagement','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19950058801&hterms=design+management&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D60%26Ntt%3Ddesign%2Bmanagement"><span>Application of capillary fluid management techniques to the design of a <span class="hlt">phase</span> <span class="hlt">separating</span> microgravity bioreactor</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Finger, Barry W.; Neville, Gale E., Jr.; Sager, John C.</p> <p>1993-01-01</p> <p>Manned space missions require the development of compact, efficient, and reliable life support systems. A number of aqueous biological conversion processes are associated with bioregenerative life support systems. Vessels, or bioreactors, capable of supporting these processes in microgravity must be developed. An annular flow bioreactor has been conceived. It has the potential to incorporate containment, <span class="hlt">phase</span> <span class="hlt">separation</span>, gas exchange, and illumination into a single vessel. The bioreactor utilizes capillary fluid management techniques and is configured as a cylindrical tube in which a two-<span class="hlt">phase</span> liquid-gas flow is maintained. Vanes placed around the inner perimeter enhance capillary forces and cause the liquid <span class="hlt">phase</span> to attach and flow along the interior surface of the tube. No physical barrier is required to complete <span class="hlt">phase</span> <span class="hlt">separation</span>. It is shown analytically that liquid film thickness is limited only by vane geometry and that an annular flow bioreactor capable of managing 284 liters would occupy 0.7 cubic m, less than half the volume of a Spacelab experiment rack.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21304517','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21304517"><span>Electronic <span class="hlt">phase</span> <span class="hlt">separation</span> at the LaAlO₃/SrTiO₃ interface.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ariando; Wang, X; Baskaran, G; Liu, Z Q; Huijben, J; Yi, J B; Annadi, A; Barman, A Roy; Rusydi, A; Dhar, S; Feng, Y P; Ding, J; Hilgenkamp, H; Venkatesan, T</p> <p>2011-02-08</p> <p>There are many electronic and magnetic properties exhibited by complex oxides. Electronic <span class="hlt">phase</span> <span class="hlt">separation</span> (EPS) is one of those, the presence of which can be linked to exotic behaviours, such as colossal magnetoresistance, metal-insulator transition and high-temperature superconductivity. A variety of new and unusual electronic <span class="hlt">phases</span> at the interfaces between complex oxides, in particular between two non-magnetic insulators LaAlO(3) and SrTiO(3), have stimulated the oxide community. However, no EPS has been observed in this system despite a theoretical prediction. Here, we report an EPS state at the LaAlO(3)/SrTiO(3) interface, where the interface charges are <span class="hlt">separated</span> into regions of a quasi-two-dimensional electron gas, a ferromagnetic <span class="hlt">phase</span>, which persists above room temperature, and a (superconductor like) diamagnetic/paramagnetic <span class="hlt">phase</span> below 60 K. The EPS is due to the selective occupancy (in the form of 2D-nanoscopic metallic droplets) of interface sub-bands of the nearly degenerate Ti orbital in the SrTiO(3). The observation of this EPS demonstrates the electronic and magnetic phenomena that can emerge at the interface between complex oxides mediated by the Ti orbital.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25423615','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25423615"><span>The relationship between oxygen permeability and <span class="hlt">phase</span> <span class="hlt">separation</span> morphology of the multicomponent silicone hydrogels.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhao, Zhengbai; Xie, Haijiao; An, Shuangshuang; Jiang, Yong</p> <p>2014-12-18</p> <p>In this article, the multicomponent copolymers were prepared by the copolymerization of two hydrophobic silicon-containing monomers bis(trimethylsilyloxy) methylsilylpropyl glycerol methacrylate (SiMA) and tris(trimethylsiloxy)-3-methacryloxypropylsilane (TRIS) with three hydrophilic monomers 2-hydroxyethyl methacrylate, N-vinylpyrrolidone, and N,N-dimethyl acrylamide. The copolymers were hydrated to form transparent silicone hydrogels. The oxygen permeability coefficients (Dk) of hydrogels were measured, and their relationships with the equilibrium water contents (EWC) and the types and contents of silicon containing monomers as well as the <span class="hlt">phase</span> <span class="hlt">separation</span> structures of silicone hydrogels were analyzed in detail. The results showed that the EWC decreased as the increase of SiMA content. The relationship between Dk and SiMA content, as well as that between Dk and EWC, showed inverted bell curve distributions, which meant two main factors, i.e., silicon-oxygen bond in silicone and water in hydrogel, contributed to oxygen permeation and followed a mutual inhibition competition mechanism. The internal morphologies of the hydrogels were observed by transmission electron microscope, and the results showed that the hydrogels presented two different <span class="hlt">phase</span> <span class="hlt">separation</span> structures depending on the types of the silicon-containing monomers. The silicone <span class="hlt">phase</span> in SiMA containing hydrogel presented to be a granular texture, while the silicone <span class="hlt">phase</span> in TRIS containing hydrogel formed a fibrous texture which resulted in a higher Dk value. These results could help to design a silicone hydrogel with better properties and wider application.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015JSP...158..589B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015JSP...158..589B"><span>Motility-Induced <span class="hlt">Phase</span> <span class="hlt">Separation</span> of Active Particles in the Presence of Velocity Alignment</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Barré, Julien; Chétrite, Raphaël; Muratori, Massimiliano; Peruani, Fernando</p> <p>2015-02-01</p> <p>Self-propelled particle (SPP) systems are intrinsically out of equilibrium systems, where each individual particle converts energy into work to move in a dissipative medium. When interacting through a velocity alignment mechanism, and with the medium acting as a momentum sink, even momentum is not conserved. In this scenario, a mapping into an equilibrium system seems unlikely. Here, we show that an entropy functional can be derived for SPPs with velocity alignment and density-dependent speed, at least in the (orientationally) disordered <span class="hlt">phase</span>. This non-trivial result has important physical consequences. The study of the entropy functional reveals that the system can undergo <span class="hlt">phase</span> <span class="hlt">separation</span> before the orientational-order <span class="hlt">phase</span> transition known to occur in SPP systems with velocity alignment. Moreover, we indicate that the spinodal line is a function of the alignment sensitivity and show that density fluctuations as well as the critical spatial diffusion, that leads to <span class="hlt">phase</span> <span class="hlt">separation</span>, dramatically increase as the orientational-order transition is approached.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1259706-pressure-induced-electronic-phase-separation-magnetism-superconductivity-cras','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1259706-pressure-induced-electronic-phase-separation-magnetism-superconductivity-cras"><span>Pressure-induced electronic <span class="hlt">phase</span> <span class="hlt">separation</span> of magnetism and superconductivity in CrAs</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Khasanov, Rustem; Guguchia, Zurab; Eremin, Ilya; ...</p> <p>2015-09-08</p> <p>We report that the recent discovery of pressure (p) induced superconductivity in the binary helimagnet CrAs has raised questions on how superconductivity emerges from the magnetic state and on the mechanism of the superconducting pairing. In the present work the suppression of magnetism and the occurrence of superconductivity in CrAs were studied by means of muon spin rotation. The magnetism remains bulk up to p ≃ 3.5 kbar while its volume fraction gradually decreases with increasing pressure until it vanishes at p ≃ 7 kbar. At 3.5 kbar superconductivity abruptly appears with its maximum Tc ≃ 1.2 K which decreasesmore » upon increasing the pressure. In the intermediate pressure region (3.5≲ p ≲ 7 kbar) the superconducting and the magnetic volume fractions are spatially <span class="hlt">phase</span> <span class="hlt">separated</span> and compete for <span class="hlt">phase</span> volume. Our results indicate that the less conductive magnetic <span class="hlt">phase</span> provides additional carriers (doping) to the superconducting parts of the CrAs sample thus leading to an increase of the transition temperature (Tc) and of the superfluid density (ρs). A scaling of ρs with Tc3.2 as well as the <span class="hlt">phase</span> <span class="hlt">separation</span> between magnetism and superconductivity point to a conventional mechanism of the Cooper-pairing in CrAs.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23496518','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23496518"><span>Structure of <span class="hlt">phase-separated</span> athermal colloid-polymer systems in the protein limit.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mahynski, Nathan A; Irick, Barry; Panagiotopoulos, Athanassios Z</p> <p>2013-02-01</p> <p>Structural features of <span class="hlt">phase-separated</span> athermal colloid-polymer mixtures in the so-called "protein limit," where polymer chain dimensions exceed those of the colloid, are investigated using grand canonical Monte Carlo simulations on a fine lattice. Previous work [N. A. Mahynski et al., Phys. Rev. E 85, 051402 (2012)] has shown that this model accurately captures the <span class="hlt">phase</span> behavior of experimental systems, and that colloids with sufficiently small diameters, σ(c), relative to that of the monomeric segments, σ(s), <span class="hlt">phase</span> <span class="hlt">separate</span> more readily than their large-diameter counterparts. In the present study, we directly connect colloid and polymer structure with their <span class="hlt">phase</span> behavior by investigating these solutions along their binodal curves; we also explore the role of colloid surface curvature in destabilizing such solutions. Our findings suggest that simple consideration of an additional depletion radius, on the order of the σ(s), leads to a quantitatively accurate prediction of the division between stable and unstable ranges of d=σ(s)/σ(c). We compare these results to continuum models with different bonding potentials between monomer segments in order to elucidate the significance of the lattice model's bond fluctuations and inherently coarse colloid surface. In a number of cases, the continuum models deviate both qualitatively and quantitatively from the lattice results, but the binodals of the continuum models are presently not known, making a strong conclusion about these differences impossible.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/22581546','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/22581546"><span><span class="hlt">Phase</span> <span class="hlt">separated</span> behavior in yttrium doped CaMnO{sub 3}</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Sharma, Neetika; Das, A.; Prajapat, C.L.; Kumar, Amit; Singh, M.R.</p> <p>2016-05-15</p> <p>Highlights: • Electron doped manganite. • Magnetic <span class="hlt">phase</span> <span class="hlt">separation</span> observed. • Structural transition coupled with magnetic transition. - Abstract: The effect of electron doping on the structural, transport, and magnetic properties of Mn (IV)—rich Ca{sub 1−x}Y{sub x}MnO{sub 3} (x ≤ 0.2) samples have been investigated using neutron diffraction, neutron depolarization, magnetization and resistivity techniques. The temperature dependence of resistivity follows the small polaron model and the activation energy exhibits a minimum for x = 0.1 sample. A <span class="hlt">phase</span> <span class="hlt">separated</span> magnetic ground state consisting of ferromagnetic domains (∼7 μm) embedded in G-type antiferromagnetic matrix is observed in the sample, x = 0.1. The transition to the long-range magnetically ordered state in this sample is preceded by a Griffith’s <span class="hlt">phase</span>. On lowering temperature below 300 K a structural transition from orthorhombic structure (Pnma) to a monoclinic structure (P2{sub 1}/m) is observed in the case of x = 0.2 sample. The ferromagnetic behavior in this case is suppressed and the antiferromagnetic ordering is described by coexisting C-type and G-type magnetic structures corresponding to the monoclinic and orthorhombic <span class="hlt">phases</span>, respectively.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27329167','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27329167"><span>Recent development in liquid chromatography stationary <span class="hlt">phases</span> for <span class="hlt">separation</span> of Traditional Chinese Medicine components.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Jin, Hongli; Liu, Yanfang; Guo, Zhimou; Wang, Jixia; Zhang, Xiuli; Wang, Chaoran; Liang, Xinmiao</p> <p>2016-10-25</p> <p>Traditional Chinese Medicine (TCM) is an ancient medical practice which has been used to prevent and cure diseases for thousands of years. TCMs are frequently multi-component systems with mainly unidentified constituents. The study of the chemical compositions of TCMs remains a hotspot of research. Different strategies have been developed to manage the significant complexity of TCMs, in an attempt to determine their constituents. Reversed-<span class="hlt">phase</span> liquid chromatography (RPLC) is still the method of choice for the <span class="hlt">separation</span> of TCMs, but has many problems related to limited selectivity. Recently, enormous efforts have been concentrated on the development of efficient liquid chromatography (LC) methods for TCMs, based on selective stationary <span class="hlt">phases</span>. This can improve the resolution and peak capacity considerably. In addition, high-efficiency stationary <span class="hlt">phases</span> have been applied in the analysis of TCMs since the invention of ultra high-performance liquid chromatography (UHPLC). This review describes the advances in LC methods in TCM research from 2010 to date, and focuses on novel stationary <span class="hlt">phases</span>. Their potential in the <span class="hlt">separation</span> of TCMs using relevant applications is also demonstrated.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11258766','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11258766"><span>Use of vancomycin silica stationary <span class="hlt">phase</span> in packed capillary electrochromatography I. Enantiomer <span class="hlt">separation</span> of basic compounds.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Desiderio, C; Aturki, Z; Fanali, S</p> <p>2001-02-01</p> <p>Chiral <span class="hlt">separation</span> of basic compounds was achieved by using 75 or 100 microm ID fused-silica capillaries packed with a vanoomycin-modified diol silica stationary <span class="hlt">phase</span>. The capillary was firstly packed for about 12 cm with a slurry mixture composed of diolsilica (3:1) then with the vancomycin modified diol-silica (3:1) (23 cm), and finally with diol-silica (3:1) for about 2 cm. Frits were prepared by a heating wire at the two ends of the capillary; the detector window was prepared at 8.5 cm from the end of the capillary where vancomycin was not present. The influence of the mobile <span class="hlt">phase</span> composition (pH and concentration, organic modifier type and concentration) on the velocity of the electroosmotic flow, chiral resolution and enantioselectivity was studied. Good enantiomeric resolution was achieved for atenolol, oxprenolol, propranolol, and venlafaxine using a mobile <span class="hlt">phase</span> composition of 100 mM ammonium acetate solution (pH 6)/water/acetonitrile (5:5:90 v/v/v) while for terbutaline a mixture of 5:15:80 v/v/v provided the best <span class="hlt">separations</span>. The use of methanol instead of acetonitrile caused a general increase of enantiomer resolution of the studied compounds together with a reduction of efficiency and detector response. However, the combination of acetonitrile and methanol in the mobile <span class="hlt">phase</span> (as, e.g., 10% methanol and 80% acetonitrile) allowed to improve the enantiomer resolution with satisfactory detector response.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21924727','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21924727"><span>High performance liquid chromatographic <span class="hlt">separations</span> of gas oil samples and their hydrotreated products using commercial normal <span class="hlt">phases</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Oro, Nicole E; Lucy, Charles A</p> <p>2011-10-28</p> <p>Three commercially available high performance liquid chromatography columns are used in normal <span class="hlt">phase</span> or quasi-normal <span class="hlt">phase</span> mode for the <span class="hlt">separation</span> of gas oil samples. The columns are tested with 20 analytical standards to determine their suitability for <span class="hlt">separations</span> of petroleum samples and their ability to <span class="hlt">separate</span> the nitrogen group-types (pyrrole and pyridine) found in petroleum. The columns studied are polymeric hypercrosslinked polystyrene (HGN), a biphenyl <span class="hlt">phase</span>, and a Chromegabond "DNAP" column from ES Industries. The HGN column <span class="hlt">separates</span> gas oils based on both ring structure and heteroatom, while the biphenyl <span class="hlt">phase</span> has low retention of most compounds studied in quasi-normal <span class="hlt">phase</span> mode. The "DNAP" column is selective for nitrogen-containing compounds, <span class="hlt">separating</span> them from PAHs as well as oxygen and sulphur compounds. Retention data of standards on all three columns is shown, along with chromatograms of gas oil samples on the HGN and "DNAP" columns.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/servlets/purl/889702','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/servlets/purl/889702"><span>Heterogeneity of the Liquid <span class="hlt">Phase</span>, and Vapor <span class="hlt">Separation</span> in Los Azufres (Mexico) Geothermal Reservoir</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Nieva, D.; Quijano, L.; Garfias, A.; Barragan, R.M.; Laredo, F.</p> <p>1983-12-15</p> <p>Data of chemical and isotopic composition of fluids from Los Azufres geothermal wells is interpreted in order to characterize the composition of the liquid <span class="hlt">phase</span>, and to define the relation between this <span class="hlt">phase</span> and fluids from steam-producing wells. Chemical and specific enthalpy data show that most wells considered are fed a mixture of steam and liquid. Thus, flashing occurs in the formation. This poses a problem on the interpretation of isotopic data, because the composition of the feeding mixture need not be representative of the composition of the liquid <span class="hlt">phase</span> in the reservoir. Two extreme alternatives for the interpretation of isotopic data are considered. In the first alternative the composition of the total discharge is considered to be the same as that of the liquid in the reservoir. In the second alternative the feeding fluid is considered to be a mixture of the liquid <span class="hlt">phase</span> in the reservoir and the calculated fraction of steam. In addition, this steam is assumed to <span class="hlt">separate</span> from a much larger mass of that liquid <span class="hlt">phase</span> at the downhole temperature. The contribution of steam is then subtracted from the total discharge to yield the composition of the liquid <span class="hlt">phase</span>. Using data for silica concentration in total discharge and <span class="hlt">separated</span> water, the chloride concentration in the reservoir liquid is calculated. This result is used to calculate the fraction of steam in the feeding mixture of each well. The isotopic data is then corrected as proposed for the second alternative, to yield the composition of the liquid <span class="hlt">phase</span>. Comparison of the corrected and uncorrected isotopic values shows that the correction has an important effect only when the steam mass fraction in the feeding mixture is large (> 20%). The correction tends to reduce the dispersion of data points in a {delta} D vs {delta}{sup 18}O diagram. Points representing composition of liquid <span class="hlt">phase</span> show an approximately linear distribution, suggesting a process of mixing of two fluids. Available data appears to</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/1239535','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/1239535"><span>Dynamic evolution of liquid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> during continuous cooling</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Imhoff, S. D.; Gibbs, P. J.; Katz, M. R.; Ott, T. J.; Patterson, B. M.; Lee, W. -K.; Fezzaa, K.; Cooley, J. C.; Clarke, A. J.</p> <p>2015-03-01</p> <p>Solidification from a multiphase fluid involves many unknown quantities due to the difficulty of predicting the impact of fluid flow on chemical partitioning. Real-time x-ray radiography has been used to observe liquideliquid <span class="hlt">phase</span> <span class="hlt">separation</span> in Al90In10 prior to solidification. Quantitative image analysis has been used to measure the motion and population characteristics of the dispersed indium-rich liquid <span class="hlt">phase</span> during cooling. Here we determine that the droplet growth characteristics resemble well known steady-state coarsening laws with likely enhancement by concurrent growth due to supersaturation. Simplistic views of droplet motion are found to be insufficient until late in the reaction due to a hydrodynamic instability caused by the large density difference between the dispersed and matrix liquid <span class="hlt">phases</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1238610-dynamic-evolution-liquidliquid-phase-separation-during-continuous-cooling','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1238610-dynamic-evolution-liquidliquid-phase-separation-during-continuous-cooling"><span>Dynamic evolution of liquid–liquid <span class="hlt">phase</span> <span class="hlt">separation</span> during continuous cooling</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Imhoff, Seth D.; Gibbs, Paul J.; Katz, Martha R.; ...</p> <p>2015-01-06</p> <p>Solidification from a multiphase fluid involves many unknown quantities due to the difficulty of predicting the impact of fluid flow on chemical partitioning. Real-time x-ray radiography was used to observe liquid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> in Al90In10 prior to solidification. Quantitative image analysis was used to measure the motion and population characteristics of the dispersed indium-rich liquid <span class="hlt">phase</span> during cooling. Here we determine that the droplet growth characteristics resemble well known steady-state coarsening laws with likely enhancement by concurrent growth due to supersaturation. Simplistic views of droplet motion are found to be insufficient until late in the reaction due to a hydrodynamicmore » instability caused by the large density difference between the dispersed and matrix liquid <span class="hlt">phases</span>.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16186910','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16186910"><span>Thermomorphic <span class="hlt">phase</span> <span class="hlt">separation</span> in ionic liquid-organic liquid systems--conductivity and spectroscopic characterization.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Riisager, Anders; Fehrmann, Rasmus; Berg, Rolf W; van Hal, Roy; Wasserscheid, Peter</p> <p>2005-08-21</p> <p>Electrical conductivity, FT-Raman and NMR measurements are demonstrated as useful tools to probe and determine <span class="hlt">phase</span> behavior of thermomorphic ionic liquid-organic liquid systems. To illustrate the methods, consecutive conductivity measurements of a thermomorphic methoxyethoxyethyl-imidazolium ionic liquid/1-hexanol system are performed in the temperature interval 25-80 degrees C using a specially constructed double-electrode cell. In addition, FT-Raman and 1H-NMR spectroscopic studies performed on the <span class="hlt">phase-separable</span> system in the same temperature interval confirm the mutual solubility of the components in the system, the liquid-liquid equilibrium <span class="hlt">phase</span> diagram of the binary mixture, and signify the importance of hydrogen bonding between the ionic liquid and the hydroxyl group of the alcohol.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/969978','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/969978"><span><span class="hlt">Phase</span> <span class="hlt">Separation</span> in the Heisenberg Spin System Gd2Ti2O7</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Ehlers, Georg</p> <p>2010-01-01</p> <p>Gd{sub 2}Ti{sub 2}O{sub 7} is a geometrically frustrated antiferromagnetic system with two magnetic <span class="hlt">phase</span> transitions at 1.1 K and 0.7 K. The determination of the magnetic structure in the ordered <span class="hlt">phases</span> by a powder measurement is greatly complicated by the ambiguity between 1-k and 4-k structures resulting in identical structure factors. Here we will present data and new analyses showing that, as the system cools from the correlated, paramagnetic regime just above 1 K, (i) the magnetic system freezes into a partially ordered state, and (ii) the 4-k structure is maintained throughout down to a base temperature <50 mK. This clears up the ambiguity in the magnetic structure and confirms the <span class="hlt">phase</span> <span class="hlt">separation</span> of the Gd-sites into two in equivalent sites with a 3:1 ratio.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/6889376','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/6889376"><span>Intensive use of biomass feedstock in ethanol conversion: The alcohol-water, vapor-<span class="hlt">phase</span> <span class="hlt">separation</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Robertson, G.H.; Doyle, L.R.; Pavlath, A.E.</p> <p>1983-12-01</p> <p>Fermentation of ethanol in a system whereby the biomass is used intensively (both to <span class="hlt">separate</span> alcohol from water by vapor <span class="hlt">phase</span> adsorption and to serve as the feedstock) is shown to be possible on theoretical grounds when the biomass is grain. The rationale for a vapor-<span class="hlt">phase</span> adsorption process as an alternative to distillation is shown to be energetically valid above 84 wt % ethanol. The capacity of grain in new vapor-<span class="hlt">phase</span> ambient adsorption processes was estimated experimentally with the finding that sufficient capacity exists for the intensive use but that the adsorption is dynamically controlled so that the grain form and particle size are important. Pretreatments such as explosive dehydration improve the transfer of water to the grain in adsorption with potential improvement in the efficiency of liquefaction and saccharification. At room temperature, these sorbents are not perfectly selective for water but adsorb ethanol which will be carried to the liquefaction, saccharification, and fermentation with the feedstock.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16965092','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16965092"><span>Gas-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> in oppositely charged colloids: stability and interfacial tension.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Fortini, Andrea; Hynninen, Antti-Pekka; Dijkstra, Marjolein</p> <p>2006-09-07</p> <p>We study the <span class="hlt">phase</span> behavior and the interfacial tension of the screened Coulomb (Yukawa) restricted primitive model (YRPM) of oppositely charged hard spheres with diameter sigma using Monte Carlo simulations. We determine the gas-liquid and gas-solid <span class="hlt">phase</span> transitions using free energy calculations and grand-canonical Monte Carlo simulations for varying inverse Debye screening length kappa. We find that the gas-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> is stable for kappasigma<or=4, and that the critical temperature decreases upon increasing the screening of the interaction (decreasing the range of the interaction). In addition, we determine the gas-liquid interfacial tension using grand-canonical Monte Carlo simulations. The interfacial tension decreases upon increasing the range of the interaction. In particular, we find that simple scaling can be used to relate the interfacial tension of the YRPM to that of the restricted primitive model, where particles interact with bare Coulomb interactions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/servlets/purl/1238610','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/servlets/purl/1238610"><span>Dynamic evolution of liquid–liquid <span class="hlt">phase</span> <span class="hlt">separation</span> during continuous cooling</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Imhoff, Seth D.; Gibbs, Paul J.; Katz, Martha R.; Ott, Thomas J.; Patterson, Brian M.; Lee, Wah-Keat; Fezzaa, Kamel; Cooley, Jason C.; Clarke, Amy J.</p> <p>2015-01-06</p> <p>Solidification from a multiphase fluid involves many unknown quantities due to the difficulty of predicting the impact of fluid flow on chemical partitioning. Real-time x-ray radiography was used to observe liquid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> in Al<sub>90</sub>In<sub>10</sub> prior to solidification. Quantitative image analysis was used to measure the motion and population characteristics of the dispersed indium-rich liquid <span class="hlt">phase</span> during cooling. Here we determine that the droplet growth characteristics resemble well known steady-state coarsening laws with likely enhancement by concurrent growth due to supersaturation. Simplistic views of droplet motion are found to be insufficient until late in the reaction due to a hydrodynamic instability caused by the large density difference between the dispersed and matrix liquid <span class="hlt">phases</span>.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_22 --> <div id="page_23" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="441"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/servlets/purl/1068840','DOE-PATENT-XML'); return false;" href="http://www.osti.gov/scitech/servlets/purl/1068840"><span><span class="hlt">Phase-separated</span>, epitaxial composite cap layers for electronic device applications and method of making the same</span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Aytug, Tolga [Knoxville, TN; Paranthaman, Mariappan Parans [Knoxville, TN; Polat, Ozgur [Knoxville, TN</p> <p>2012-07-17</p> <p>An electronic component that includes a substrate and a <span class="hlt">phase-separated</span> layer supported on the substrate and a method of forming the same are disclosed. The <span class="hlt">phase-separated</span> layer includes a first <span class="hlt">phase</span> comprising lanthanum manganate (LMO) and a second <span class="hlt">phase</span> selected from a metal oxide (MO), metal nitride (MN), a metal (Me), and combinations thereof. The <span class="hlt">phase-separated</span> material can be an epitaxial layer and an upper surface of the <span class="hlt">phase-separated</span> layer can include interfaces between the first <span class="hlt">phase</span> and the second <span class="hlt">phase</span>. The <span class="hlt">phase-separated</span> layer can be supported on a buffer layer comprising a composition selected from the group consisting of IBAD MgO, LMO/IBAD-MgO, homoepi-IBAD MgO and LMO/homoepi-MgO. The electronic component can also include an electronically active layer supported on the <span class="hlt">phase-separated</span> layer. The electronically active layer can be a superconducting material, a ferroelectric material, a multiferroic material, a magnetic material, a photovoltaic material, an electrical storage material, and a semiconductor material.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27650633','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27650633"><span>Two-<span class="hlt">phase</span> anaerobic digestion of vegetable market waste fraction of municipal solid waste and development of improved technology for <span class="hlt">phase</span> <span class="hlt">separation</span> in two-<span class="hlt">phase</span> reactor.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Majhi, Bijoy Kumar; Jash, Tushar</p> <p>2016-12-01</p> <p>Biogas production from vegetable market waste (VMW) fraction of municipal solid waste (MSW) by two-<span class="hlt">phase</span> anaerobic digestion system should be preferred over the single-stage reactors. This is because VMW undergoes rapid acidification leading to accumulation of volatile fatty acids and consequent low pH resulting in frequent failure of digesters. The weakest part in the two-<span class="hlt">phase</span> anaerobic reactors was the techniques applied for solid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> of digestate in the first reactor where solubilization, hydrolysis and acidogenesis of solid organic waste occur. In this study, a two-<span class="hlt">phase</span> reactor which consisted of a solid-<span class="hlt">phase</span> reactor and a methane reactor was designed, built and operated with VMW fraction of Indian MSW. A robust type filter, which is unique in its implementation method, was developed and incorporated in the solid-<span class="hlt">phase</span> reactor to <span class="hlt">separate</span> the process liquid produced in the first reactor. Experiments were carried out to assess the long term performance of the two-<span class="hlt">phase</span> reactor with respect to biogas production, volatile solids reduction, pH and number of occurrence of clogging in the filtering system or choking in the process liquid transfer line. The system performed well and was operated successfully without the occurrence of clogging or any other disruptions throughout. Biogas production of 0.86-0.889m(3)kg(-1)VS, at OLR of 1.11-1.585kgm(-3)d(-1), were obtained from vegetable market waste, which were higher than the results reported for similar substrates digested in two-<span class="hlt">phase</span> reactors. The VS reduction was 82-86%. The two-<span class="hlt">phase</span> anaerobic digestion system was demonstrated to be stable and suitable for the treatment of VMW fraction of MSW for energy generation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23676903','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23676903"><span>Fabrication of poly(γ-glutamic acid) monolith by thermally induced <span class="hlt">phase</span> <span class="hlt">separation</span> and its application.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Park, Sung-Bin; Fujimoto, Takashi; Mizohata, Eiichi; Inoue, Tsuyoshi; Sung, Moon-Hee; Uyama, Hiroshi</p> <p>2013-01-01</p> <p>Monoliths are functional porous materials with a three-dimensional continuous interconnected pore structure in a single piece. A monolith with uniform shape based on poly(γ-glutamic acid) (PGA) has been prepared via a thermally induced <span class="hlt">phase</span> <span class="hlt">separation</span> technique using a mixture of dimethyl sulfoxide, water, and ethanol as solvent. The morphology of the obtained monolith was observed by scanning electron microscopy and the surface area of the monolith was evaluated by the Brunauer Emmett Teller method. The effects of fabrication parameters such as the concentration and molecular mass of PGA and the solvent composition have been systematically investigated. The PGA monolith was cross-linked with hexamethylene diisocyanate to produce the water-insoluble monolith. The addition of sodium chloride to the <span class="hlt">phase</span> <span class="hlt">separation</span> solvent affected the properties of the cross-linked monolith. The swelling ratio of the cross-linked monolith toward aqueous solutions depended on the buffer pH as well as the monolith fabrication condition. Copper(II) ion was efficiently adsorbed on the cross-linked PGA monolith, and the obtained copper-immobilized monolith showed strong antibacterial activity for Escherichia coli. By combination of the characteristic properties of PGA (e.g., high biocompatibility and biodegradability) and the unique features of monoliths (e.g., through-pore structure, large surface area, and high porosity with small pore size), the PGA monolith possesses large potentials for various industrial applications in the biomedical, environmental, analytical, and <span class="hlt">separation</span> fields.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20010069258','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20010069258"><span>Normal Gravity Testing of a Microchannel <span class="hlt">Phase</span> <span class="hlt">Separator</span> for In Situ Resource Utilization</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>TeGrotenhuis, Ward E.; Stenkamp, Victoria S.; McQuillen, John (Technical Monitor)</p> <p>2001-01-01</p> <p>A microchannel <span class="hlt">separator</span>, with 2.7 millimeters as the smallest dimension, was tested, and a pore throat structure captured and removed liquid from a gas-liquid stream. The microchannel device was tested over a of gas and liquid flow rates ranging from 0.0005 up to 0. 14 volume fraction of liquid. Four liquids were tested with air. The biggest factor affecting the throughput is the capacity of liquid flow through the pore throat, which is dictated by permeability, liquid viscosity, flow area, pore throat thickness, and pressure difference across the pore throat. Typically, complete <span class="hlt">separation</span> of gas and liquid fractions was lost when the liquid flow rate reached about 40 to 60% of the pore throat capacity. However, this could occur over a range of 10 to 90% utilization of pore throat capacity. Breakthrough occurs in the microchannel <span class="hlt">phase</span> <span class="hlt">separator</span> at conditions similar to the annular to plug flow transition of two-<span class="hlt">phase</span> microgravity pipe flow implying that operating in the proper flow regime is crucial. Analysis indicates that the Bond number did not affect performance, supporting the premise that hydrodynamic, interfacial, and capillary forces are more important than gravity. However, the relative importance of gravity is better discerned through testing under reduced gravity conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1990PhDT.......162M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1990PhDT.......162M"><span><span class="hlt">Phase</span> <span class="hlt">Separation</span> in Indium Gallium Arsenide and Indium Gallium Arsenic Phosphide Epitaxial Films.</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>McDevitt, Thomas L.</p> <p>1990-01-01</p> <p>Microstructures of InGaAs and InGaAsP epitaxial layers have been investigated to study the <span class="hlt">phase</span> <span class="hlt">separation</span> reaction that occurs in these materials. InGaAsP layers have been grown by liquid <span class="hlt">phase</span> epitaxy on (001), (110), (111), and (123) oriented InP substrates and have been characterized by plan view and cross sectional transmission electron microscopy. Results indicate that the fine scale contrast modulations are two dimensional and lie in the plane of the substrate surface. The crystallographic alignment of these modulations has been shown to be determined by the elastic anisotropy of the substrate crystal in the growth plane. The coarse modulations that are commonly observed in (001) samples are not found in layers grown on the other orientations. It is proposed that the coarse modulations are the result of a buckling reaction which occurs as a result of the fine scale modulations. Representative molecular beam epitaxy and metallorganic chemical vapor deposition grown samples have also been examined and confirm that the LPE results are generic in nature. Annealing studies have also been carried out on <span class="hlt">phase</span> <span class="hlt">separated</span> InGaAsP layers to study the reversion phenomenon. The conditions that are required to accomplish homogenization reflect the very slow interdiffusion rates in these materials. Consideration of the annealing results establishes that the rates of mass transfer by bulk diffusion are too low to allow the <span class="hlt">phase</span> <span class="hlt">separation</span> reaction to occur by this mechanism. Hall effect measurements show that the carrier mobility increases on annealing and that a concurrent increase in carrier concentration is also observed. Photoluminescence measurements reveal a broadening of the band to band transition peak following the anneal. Finally, the effects of zinc diffusion on <span class="hlt">phase</span> <span class="hlt">separated</span> microstructures in InGaAs and InGaAsP layers have also been analyzed. It is shown that the diffusion of zinc into these materials can also homogenize the modulations. For the In</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011NJPh...13k5013C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011NJPh...13k5013C"><span>Emergence of microstructural patterns in skin cancer: a <span class="hlt">phase</span> <span class="hlt">separation</span> analysis in a binary mixture</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Chatelain, C.; Balois, T.; Ciarletta, P.; Ben Amar, M.</p> <p>2011-11-01</p> <p>Clinical diagnosis of skin cancers is based on several morphological criteria, among which is the presence of microstructures (e.g. dots and nests) sparsely distributed within the tumour lesion. In this study, we demonstrate that these patterns might originate from a <span class="hlt">phase</span> <span class="hlt">separation</span> process. In the absence of cellular proliferation, in fact, a binary mixture model, which is used to represent the mechanical behaviour of skin cancers, contains a cell-cell adhesion parameter that leads to a governing equation of the Cahn-Hilliard type. Taking into account a reaction-diffusion coupling between nutrient consumption and cellular proliferation, we show, with both analytical and numerical investigations, that two-<span class="hlt">phase</span> models may undergo a spinodal decomposition even when considering mass exchanges between the <span class="hlt">phases</span>. The cell-nutrient interaction defines a typical diffusive length in the problem, which is found to control the saturation of a growing <span class="hlt">separated</span> domain, thus stabilizing the microstructural pattern. The distribution and evolution of such emerging cluster morphologies, as predicted by our model, are successfully compared to the clinical observation of microstructural patterns in tumour lesions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005PhRvE..72f1603D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005PhRvE..72f1603D"><span>Kinetics of <span class="hlt">phase</span> <span class="hlt">separation</span> in thin films: Simulations for the diffusive case</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Das, Subir K.; Puri, Sanjay; Horbach, Jürgen; Binder, K.</p> <p>2005-12-01</p> <p>We study the diffusion-driven kinetics of <span class="hlt">phase</span> <span class="hlt">separation</span> of a symmetric binary mixture (AB) , confined in a thin-film geometry between two parallel walls. We consider cases where (i) both walls preferentially attract the same component (A) , and (ii) one wall attracts A and the other wall attracts B (with the same strength). We focus on the interplay of <span class="hlt">phase</span> <span class="hlt">separation</span> and wetting at the walls, which is referred to as surface-directed spinodal decomposition (SDSD). The formation of SDSD waves at the two surfaces, with wave vectors oriented perpendicular to them, often results in a metastable layered state (also referred to as “stratified morphology”). This state is reminiscent of the situation where the thin film is still in the one-<span class="hlt">phase</span> region but the surfaces are completely wet, and hence coated with thick wetting layers. This metastable state decays by spinodal fluctuations and crosses over to an asymptotic growth regime characterized by the lateral coarsening of pancakelike domains. These pancakes may or may not be coated by precursors of wetting layers. We use Langevin simulations to study this crossover and the growth kinetics in the asymptotic coarsening regime.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2002APS..MAR.J2006K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2002APS..MAR.J2006K"><span>Pattern Polymerization-Induced <span class="hlt">Phase</span> <span class="hlt">Separation</span> in a Polymer-Dispersed Liquid Crystal System</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kyu, Thein</p> <p>2002-03-01</p> <p>Liquid crystal (LC)/polymer composite films have gained attention increasingly due to their applications in flat panel displays and shutters. Photopolymerization is a preferred method to produce LC/polymer composite films from mixtures of reactive monomers and LCs. On the basis of the combined Flory-Huggins free energy for isotropic mixing and Maier-Saupe free energy for nematic ordering along with the elastic free energy of the network, <span class="hlt">phase</span> diagrams have been established by solving self-consistently. A theoretical simulation has been modeled by incorporating the kinetics of crosslinking reaction into the time-dependent Ginzburg-Landau (TDGL-model C) equations to elucidate the emergence of nematic domains during photopolymerization induced <span class="hlt">phase</span> <span class="hlt">separation</span> in electrically switchable holographic polymer-dispersed liquid crystals (H-PDLC). The simulated morphological patterns in the concentration and orientation order parameter fields show discrete layers of liquid crystal droplets alternating periodically with polymer network-rich layers. Furthermore, we recognized the potential for producing electrically tunable microlens from PDLC systems through pattern-photopolymerization-induced <span class="hlt">phase</span> <span class="hlt">separation</span> by means of the interference of two horizontal waves and two vertical waves. Our simulation revealed that the emerged LC microlens are of the order of a few hundred nanometers. These LC microlens are not only uniformed in size, but also form in regular arrays, reminiscence of the compound eyes found in flies, ants, and wasps. Supported by ALCOM, NSF DMR 99-03519, and OBR.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013GeoRL..40.3496S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013GeoRL..40.3496S"><span>First calculation of <span class="hlt">phase</span> and coherence of longitudinally <span class="hlt">separated</span> L-band equatorial ionospheric scintillation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Shume, E. B.; Mannucci, A. J.</p> <p>2013-07-01</p> <p>We present the first calculation of <span class="hlt">phase</span> and coherence of cross-wavelet transform applied to longitudinally <span class="hlt">separated</span> L-band equatorial ionospheric scintillation observations received from Geostationary Earth Orbit (GEO) satellites. The <span class="hlt">phase</span> and coherence analysis were employed on two pairs of observations: (1) São Luís and Rio Branco and (2) Alta Floresta and Huancayo. For these case studies, in statistically significant and high-coherence regions, scintillation observations over São Luís (Alta Floresta) lead that of Rio Branco (Huancayo) by ˜2 to 3 h with a 95%frequency. If L-band scintillation happens over São Luís (Alta Floresta), there is a 95%likelihood that scintillation would happen to the west over Rio Branco (Huancayo) after ˜2 to 3 h, suggesting that a forecast can be made ahead of scintillation occurrences. The <span class="hlt">phase</span> and coherence relationships between the longitudinally <span class="hlt">separated</span> scintillation-producing regions can be connected to the large-scale wave structures which are reported to be related to the generation of equatorial spread F and scintillation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/10867184','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/10867184"><span>Gelation by <span class="hlt">phase</span> <span class="hlt">separation</span> in a whey protein system: in-situ kinetics of aggregation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Renard, D; Robert, P; Garnier, C; Dufour, E; Lefebvre, J</p> <p>2000-05-26</p> <p>The aggregation and gelation properties of beta-lactoglobulin (BLG), a globular protein from milk, was studied in aqueous ethanol solutions at room temperature. The <span class="hlt">phase</span> state diagrams as a function of pH and ethanol concentration showed that a gel structure appeared after a period ranging from 1 min to 1 week, depending on the physico-chemical conditions. The in-situ kinetics of aggregation were followed by several methods in order to obtain a better understanding of the building of aggregates by the addition of ethanol. It was shown that the aggregation kinetics highly depended upon the pH, the process being fastest at pH 7. Viscoelasticity and infrared measurements indicated that alcohol-induced gelation would proceed via a two-step mechanism: small aggregates loosely connected between them were first built up; a real network took place in a second step. The coarse and irregular structures formed in aqueous ethanol gels revealed by confocal laser scanning microscopy could be analysed in terms of a <span class="hlt">phase</span> <span class="hlt">separation</span>. This observation was supported by a syneresis phenomenon visible in the final gel state. BLG in water-ethanol solution would undergo either an inhibition of the demixing by gelation or a binary <span class="hlt">phase</span> <span class="hlt">separation</span> accompanied by an irreversible gelation transition.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016SPIE.9718E..2SL','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016SPIE.9718E..2SL"><span>Direct single-shot <span class="hlt">phase</span> retrieval for <span class="hlt">separated</span> objects (Conference Presentation)</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Leshem, Ben; Xu, Rui; Miao, Jianwei; Nadler, Boaz; Oron, Dan; Dudovich, Nirit; Raz, Oren</p> <p>2016-03-01</p> <p>The <span class="hlt">phase</span> retrieval problem arises in various fields ranging from physics and astronomy to biology and microscopy. Computational reconstruction of the Fourier <span class="hlt">phase</span> from a single diffraction pattern is typically achieved using iterative alternating projections algorithms imposing a non-convex computational challenge. A different approach is holography, relying on a known reference field. Here we present a conceptually new approach for the reconstruction of two (or more) sufficiently <span class="hlt">separated</span> objects. In our approach we combine the constraint the objects are finite as well as the information in the interference between them to construct an overdetermined set of linear equations. We show that this set of equations is guaranteed to yield the correct solution almost always and that it can be solved efficiently by standard numerical algebra tools. Essentially, our method combine commonly used constraint (that the object is finite) with a holographic approach (interference information). It differs from holographic methods in the fact that a known reference field is not required, instead the unknown objects serve as reference to one another (hence blind holography). Our method can be applied in a single-shot for two (or more) <span class="hlt">separated</span> objects or with several measurements with a single object. It can benefit <span class="hlt">phase</span> imaging techniques such as Fourier phytography microscopy, as well as coherent diffractive X-ray imaging in which the generation of a well-characterized, high resolution reference beam imposes a major challenge. We demonstrate our method experimentally both in the optical domain and in the X-ray domain using XFEL pulses.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19548276','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19548276"><span>Spatiotemporal control of apical and basal living subcellular chemical environments through vertical <span class="hlt">phase</span> <span class="hlt">separation</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yang, Jui-Ming; Didier, Jonathan E; Cassino, Theresa R; LeDuc, Philip R</p> <p>2009-09-01</p> <p>Molecular distribution within living cells is organized through multiscaled compartmentalization that enables specialized processes to occur with high efficiency. The ability to control the chemical environment at a subcellular level is limited due to deficient positional control over the aqueous stimulant. Here, a multilayered microfluidic system built from polydimethylsiloxane to <span class="hlt">separate</span> chemical stimulants over single living cells vertically through aqueous-<span class="hlt">phase</span> <span class="hlt">separation</span> under laminar flow is demonstrated. Cells are cultured on top of single micrometer-scale channels inside a larger channel, allowing labeling of the apical domain of single cells through the main channel with simultaneous and distinct labeling of the basal domain via the lower microchannels. The system is transparent, which allows the use of optical microscopy to investigate the spatiotemporal response of labeled components. By employing this technique, the examination of localized subcellular domain responses in polarization, lipid bilayer mobility, and apical-to-basal signal transduction can be explored.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015NatSR...511523T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015NatSR...511523T"><span>Engineering Cyclodextrin Clicked Chiral Stationary <span class="hlt">Phase</span> for High-Efficiency Enantiomer <span class="hlt">Separation</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Tang, Jian; Zhang, Shapopeng; Lin, Yuzhou; Zhou, Jie; Pang, Limin; Nie, Xuemei; Zhou, Baojing; Tang, Weihua</p> <p>2015-08-01</p> <p>The <span class="hlt">separation</span> of racemic molecules is of crucial significance not only for fundamental research but also for technical application. Enantiomers remain challenging to be <span class="hlt">separated</span> owing to their identical physical and chemical properties in achiral environments. Chromatographic techniques employing chiral stationary <span class="hlt">phases</span> (CSPs) have been developed as powerful tools for the chiral analysis and preparation of pure enantiomers, most of which are of biological and pharmaceutical interests. Here we report our efforts in developing high-performance phenylcarbamated cyclodextrin (CD) clicked CSPs. Insights on the impact of CD functionalities in structure design are provided. High-efficiency enantioseparation of a range of aryl alcohols and flavanoids with resolution values (Rs) over 10 were demonstrated by per(3-chloro-4-methyl)phenylcarbamated CD clicked CSP. Comparison study and molecular simulations suggest the improved enantioselectivity was attributed to higher interactions energy difference between the complexes of enantiomers and CSPs with phenylcarbamated CD bearing 3-chloro and 4-methyl functionalities.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24975777','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24975777"><span>Evaluation of the <span class="hlt">separation</span> performance of polyvinylpyrrolidone as a virtual stationary <span class="hlt">phase</span> for chromatographic NMR.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Huang, Shaohua; Wu, Rui; Bai, Zhengwu; Yang, Ying; Li, Suying; Dou, Xiaowei</p> <p>2014-09-01</p> <p>Polyvinylpyrrolidone (PVP) was used as a virtual stationary <span class="hlt">phase</span> to <span class="hlt">separate</span> p-xylene, benzyl alcohol, and p-methylphenol by the chromatographic NMR technique. The effects of concentration and weight-average molecular weight (Mw) of PVP, solvent viscosity, solvent polarity, and sample temperature on the resolution of these components were investigated. It was found that both higher PVP concentration and higher PVP Mw caused the increase of diffusion resolution for the three components. Moreover, the diffusion resolution did not change at viscosity-higher solvents. Moreover, the three components showed different resolution at different solvents. As temperature increased, the diffusion resolution between p-xylene and benzyl alcohol gradually increased, and the one between p-xylene and p-methylphenol slightly increased from 278 to 298 K and then decreased above 298 K. It was also found that the polarity of the analytes played an important role for the <span class="hlt">separation</span> by affecting the diffusion coefficient.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23775526','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23775526"><span>Graphene nanoparticles as pseudostationary <span class="hlt">phase</span> for the electrokinetic <span class="hlt">separation</span> of nonsteroidal anti-inflammatory drugs.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Benítez-Martínez, Sandra; Simonet, Bartolomé M; Valcárcel, Miguel</p> <p>2013-09-01</p> <p>The exceptional properties of graphene (G) were exploited here to facilitate capillary electrokinetic <span class="hlt">separations</span>. Two types of commercially available G consisting of nanoparticles containing-one to three and-four to six G sheets, respectively, were compared for this purpose. Both proved effective in <span class="hlt">separating</span> the arylpropyl derivatives of nonsteroidal anti-inflammatory drugs. The highest resolution and shortest migration times were obtained with G containing high amount of single and double G nanosheets. G affords higher resolution than other types of nanoparticles; stable suspensions can be easily prepared and used as BGE without the need of adding an additional surfactant. This results in a high reproducibility in migration times and stability in background noise. The LOD and LOQ obtained by using G nanoparticles as pseudostationary <span class="hlt">phases</span> spanned the range 0.29-1.18 mg/L and 0.95-3.95 mg/L, respectively, and the RSD was less than 4.7% in all instances.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016JPhB...49q5101P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016JPhB...49q5101P"><span>N-block <span class="hlt">separable</span> random <span class="hlt">phase</span> approximation: dipole oscillations in sodium clusters and {C}_{60} fullerene</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Palade, D. I.; Baran, V.</p> <p>2016-09-01</p> <p>We generalize the schematic model based on the Random <span class="hlt">Phase</span> Approximation (RPA) with <span class="hlt">separable</span> interaction, to a collection of subspaces of ph excitations which interact with different coupling constants. This ansatz notably lowers the numerical effort involved, by reducing the RPA eigenvalue problem to a finite small dimensional system of equation. We derive the associated dispersion relation and the normalization condition for the newly defined unknowns of the system. In contrast with the standard <span class="hlt">separable</span> approach, the present formalism is able to describe more than one collective excitation even in the degenerate limit, giving also access to the nature of the resonance. The theoretical framework is tested investigating the dipolar oscillations in various neutral and singly charged sodium clusters and C 60 fullerene with results in good agreement with full RPA calculations and experimental data. It is proven that the 40 eV resonance present in photoabsorption spectra of C 60 is a localized surface plasmon.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013APS..MAR.H1313J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013APS..MAR.H1313J"><span><span class="hlt">Phase</span> <span class="hlt">separation</span> dynamics in polymer blends close to Tg: aging and rejuvenating</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Julien, Gregoire</p> <p>2013-03-01</p> <p>We extend the Percolation of Free Volume Distribution (PFVD) model developed by Long and co-workers to deal with polymer blends dynamics close to the glass transition. The dynamical model incorporates an extension of the Flory Huggins model to the case of compressible blends for calculating the driving forces. Spatial dynamics follows then from an Onsager like description. The model is solved on a 2D lattice corresponding to spatial scales of about a few tens to 100 nm and a resolution corresponding to the scale of dynamical heterogeneities, allowing to study <span class="hlt">phase</span> <span class="hlt">separation</span> close to Tg. We study also the reverse process, after the temperature is increased again in the totally miscible range. We observe a temporal asymmetry between the aging and the rejuvenation dynamics: the slow domains melt much faster than the elapsed time required to built them during the <span class="hlt">separation</span> process and total miscibility is recovered after a much shorter time.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18964971','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18964971"><span><span class="hlt">Separation</span> of some platinum metal 8-hydroxyquinolinates by normal <span class="hlt">phase</span> high-performance liquid chromatography.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Alimarinod, I P; Basova, E M; Malykhin, A Y; Bol'shova, T A</p> <p>1990-05-01</p> <p>The method of normal <span class="hlt">phase</span> high-performance liquid chromatography has been applied to the <span class="hlt">separation</span> and determination of Pd(II), Pt(II), Rh(III), Ir(IV), Ru(III) and Os(IV) as chelates with 8-hydroxyquinoline on a 62 x 2 mm column packed with Silasorb 600 5 mu silica gel by elution with methylene chloride-isopropyl alcohol mixture (97:3 v/v). The detection limits (ng per 5 mul), were Pd 0.3, Pt 1.0, Rh 1.0, Ir 5.0, Ru 1.5, Os 25. The <span class="hlt">separation</span> time was 12 min at a flow-rate of 0.1 ml/min.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25467509','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25467509"><span><span class="hlt">Separation</span> properties of saccharides on a hydrophilic stationary <span class="hlt">phase</span> having hydration layer formed zwitterionic copolymer.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kamichatani, Waka; Inoue, Yoshinori; Yamamoto, Atsushi</p> <p>2015-01-01</p> <p>A novel water-holding adsorbent bonded with a zwitterionic polymer, diallylamine-maleic acid copolymer, was developed. With this adsorbent, hydrophilic solutes are partitioned by a hydration layer that forms on the zwitterions, as a main <span class="hlt">separating</span> force. When the adsorbent was used to <span class="hlt">separate</span> saccharides by normal-<span class="hlt">phase</span> partition chromatography, the saccharides eluted in the order, mono-, di- and trisaccharide. The elution profile for mono- and di-saccharides was similar but not identical to that on anion exchange columns. This indicated that the adsorbent exhibited a complex retention behavior by the existence of both anion and cation exchange moieties in the functional polymer. Selecting Na(+) as a counter-ion of the maleate moiety enhanced the retention of saccharide. When used in an high performance liquid chromatography (HPLC) system with gradient elution, the adsorbent enabled the simultaneous analysis of mono-, di- and oligosaccharides.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19910008809','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19910008809"><span>Fluid <span class="hlt">Phase</span> <span class="hlt">Separation</span> (FPS) experiment for flight on the shuttle in a Get Away Special (GAS) canister: Design and fabrication</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p></p> <p>1990-01-01</p> <p>The <span class="hlt">separation</span> of fluid <span class="hlt">phases</span> in microgravity environments is of importance to environmental control and life support systems (ECLSS) and materials processing in space. A successful fluid <span class="hlt">phase</span> <span class="hlt">separation</span> experiment will demonstrate a proof of concept for the <span class="hlt">separation</span> technique and add to the knowledge base of material behavior. The <span class="hlt">phase</span> <span class="hlt">separation</span> experiment will contain a premixed fluid that will be exposed to a microgravity environment. After the <span class="hlt">phase</span> <span class="hlt">separation</span> of the compound has occurred, small samples of each of the species will be taken for analysis on Earth. By correlating the time of <span class="hlt">separation</span> and the temperature history of the fluid, it will be possible to characterize the process. The <span class="hlt">phase</span> <span class="hlt">separation</span> experiment is totally self-contained, with three levels of containment on all fluids, and provides all necessary electrical power and control. The controller regulates the temperature of the fluid and controls data logging and sampling. An astronaut-activated switch will initiate the experiment and an unmaskable interrupt is provided for shutdown. The experiment has been integrated into space available on a manifested Get Away Special (GAS) experiment, CONCAP 2, part of the Consortium for Materials Complex Autonomous Payload (CAP) Program, scheduled for STS 42 in April 1991. Presented here are the design and the production of a fluid <span class="hlt">phase</span> <span class="hlt">separation</span> experiment for rapid implementation at low cost.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_23 --> <div id="page_24" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="461"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22181315','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22181315"><span><span class="hlt">Phase</span> <span class="hlt">separation</span> in thermal systems: a lattice Boltzmann study and morphological characterization.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gan, Yanbiao; Xu, Aiguo; Zhang, Guangcai; Li, Yingjun; Li, Hua</p> <p>2011-10-01</p> <p>We investigate thermal and isothermal symmetric liquid-vapor <span class="hlt">separations</span> via a fast Fourier transform thermal lattice Boltzmann (FFT-TLB) model. Structure factor, domain size, and Minkowski functionals are employed to characterize the density and velocity fields, as well as to understand the configurations and the kinetic processes. Compared with the isothermal <span class="hlt">phase</span> <span class="hlt">separation</span>, the freedom in temperature prolongs the spinodal decomposition (SD) stage and induces different rheological and morphological behaviors in the thermal system. After the transient procedure, both the thermal and isothermal <span class="hlt">separations</span> show power-law scalings in domain growth, while the exponent for thermal system is lower than that for isothermal system. With respect to the density field, the isothermal system presents more likely bicontinuous configurations with narrower interfaces, while the thermal system presents more likely configurations with scattered bubbles. Heat creation, conduction, and lower interfacial stresses are the main reasons for the differences in thermal system. Different from the isothermal case, the release of latent heat causes the changing of local temperature, which results in new local mechanical balance. When the Prandtl number becomes smaller, the system approaches thermodynamical equilibrium much more quickly. The increasing of mean temperature makes the interfacial stress lower in the following way: σ=σ(0)[(T(c)-T)/(T(c)-T(0))](3/2), where T(c) is the critical temperature and σ(0) is the interfacial stress at a reference temperature T(0), which is the main reason for the prolonged SD stage and the lower growth exponent in the thermal case. Besides thermodynamics, we probe how the local viscosities influence the morphology of the <span class="hlt">phase</span> <span class="hlt">separating</span> system. We find that, for both the isothermal and thermal cases, the growth exponents and local flow velocities are inversely proportional to the corresponding viscosities. Compared with the isothermal case, the</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21709330','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21709330"><span>Hydration, <span class="hlt">phase</span> <span class="hlt">separation</span> and nonlinear rheology of temperature-sensitive water-soluble polymers.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Tanaka, Fumihiko; Koga, Tsuyoshi; Kaneda, Isamu; Winnik, Françoise M</p> <p>2011-07-20</p> <p>The collapse of a poly(N-isopropylacrylamide) (PNIPAM) chain upon heating and the <span class="hlt">phase</span> diagrams of aqueous PNIPAM solutions with a very flat lower critical solution temperature (LCST) <span class="hlt">phase</span> <span class="hlt">separation</span> line are theoretically studied on the basis of cooperative dehydration (simultaneous dissociation of bound water molecules in a group of correlated sequence), and compared with the experimental observation of temperature-induced coil-globule transition by light scattering methods. The transition becomes sharper with the cooperativity parameter σ of hydration. The reentrant coil-globule-coil transition and cononsolvency in a mixed solvent of water and methanol are also studied from the viewpoint of competitive hydrogen bonds between polymer-water and polymer-methanol. The downward shift of the cloud-point curves (LCST cononsolvency) with the mol fraction of methanol due to the competition is calculated and compared with the experimental data. Aqueous solutions of hydrophobically modified PNIPAM carrying short alkyl chains at both chain ends (telechelic PNIPAM) are theoretically and experimentally studied. The LCST of these solutions is found to shift downward along the sol-gel transition curve as a result of end-chain association (association-induced <span class="hlt">phase</span> <span class="hlt">separation</span>), and <span class="hlt">separate</span> from the coil-globule transition line. Associated structures in the solution, such as flower micelles, mesoglobules, and higher fractal assembly, are studied by ultra small-angle neutron scattering with theoretical modeling of the scattering function. Dynamic-mechanical modulus, nonlinear stationary viscosity, and stress build-up in start-up shear flows of the associated networks are studied on the basis of the affine and non-affine transient network theory. The molecular conditions for thickening, strain hardening, and stress overshoot are found in terms of the nonlinear amplitude A of the chain tension and the tension-dissociation coupling constant g.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23352803','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23352803"><span><span class="hlt">Phase</span> <span class="hlt">separation</span> in equiatomic AlCoCrFeNi high-entropy alloy.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Manzoni, A; Daoud, H; Völkl, R; Glatzel, U; Wanderka, N</p> <p>2013-09-01</p> <p>The microstructure of the as-cast AlCoCrFeNi high entropy alloy has been investigated by transmission electron microscopy and atom probe tomography. The alloy shows a very pronounced microstructure with clearly distinguishable dendrites and interdendrites. In both regions a <span class="hlt">separation</span> into an Al-Ni rich matrix and Cr-Fe-rich precipitates can be observed. Moreover, fluctuations of single elements within the Cr-Fe rich <span class="hlt">phase</span> have been singled out by three dimensional atom probe measurements. The results of investigations are discussed in terms of spinodal decomposition of the alloying elements inside the Cr-Fe-rich precipitates.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AIPC.1738U0114K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AIPC.1738U0114K"><span>Preconditioners based on approximation of non-standard norms for <span class="hlt">phase</span> <span class="hlt">separation</span> applications</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kumar, Pawan</p> <p>2016-06-01</p> <p>Some of the <span class="hlt">phase</span> <span class="hlt">separation</span> processes are typically modeled by well known Cahn-Hilliard equation with obstacle potential. Solving these equations correspond to a nonsmooth and nonlinear optimization problem. Recently a globally convergent Newton Schur method was proposed for the non-linear Schur complement corresponding to this 2 × 2 non-linear system. The discrete linear problem has essentially three parameters: the mesh size, time step, and a parameter related to interface width. The preconditioners considered so far has not been robust to one of these parameters. We propose preconditioners that seem to be robust provided the mesh is sufficiently refined.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/478794','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/478794"><span>Enantiomeric <span class="hlt">separations</span> using bovine serum albumin immobilized on ion-exchange stationary <span class="hlt">phases</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Jacobson, S.C.; Guiochon, G. |</p> <p>1992-07-01</p> <p>Bovine serum albumin (BSA) can be readily immobilized on ion-exchange stationary <span class="hlt">phases</span> by frontal analysis of a proper solution. This provides a simple means of adjusting the amount of BSA contained in the column and of measuring it accurately. Although the immobilization is ionic and not covalent, the columns are stable for extensive periods of time. If needed, they can be easily regenerated by the same frontal analysis procedure. Results for the <span class="hlt">separation</span> of various organic compounds on these columns are reported. 11 refs., 3 figs., 2 tabs.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015PhRvE..92b2124M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015PhRvE..92b2124M"><span>Dimensionality dependence of aging in kinetics of diffusive <span class="hlt">phase</span> <span class="hlt">separation</span>: Behavior of order-parameter autocorrelation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Midya, Jiarul; Majumder, Suman; Das, Subir K.</p> <p>2015-08-01</p> <p>Behavior of two-time autocorrelation during the <span class="hlt">phase</span> <span class="hlt">separation</span> in solid binary mixtures is studied via numerical solutions of the Cahn-Hilliard equation as well as Monte Carlo simulations of the Ising model. Results are analyzed via state-of-the-art methods, including the finite-size scaling technique. Full forms of the autocorrelation in space dimensions 2 and 3 are obtained empirically. The long-time behavior is found to be power law, with exponents unexpectedly higher than the ones for the ferromagnetic ordering. Both Cahn-Hilliard and Ising models provide consistent results.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17781466','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17781466"><span>Potassium, rubidium, strontium, barium, and rare-Earth concentrations in lunar rocks and <span class="hlt">separated</span> <span class="hlt">phases</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Philpotts, J A; Schnetzler, C C</p> <p>1970-01-30</p> <p>Concentrations of potassium, rubidium, strontium, barium, and rareearth elements have been determined by mass spectrometric isotope dilution for eight Apollo 11 lunar samples and for some <span class="hlt">separated</span> <span class="hlt">phases</span>. Potassiumn and ritbidium are at chondritic levels, strontium at 15 times, and barium and rare earths at 30 to 100 times chondritic levels. There are trace element similarities between the lunar samples and basaltic achondrites, terrestrial dredge basalts and the bulk earth. The trace element data appear to be consistent with these lunar samples being the result of limited partial fusion of some material similar to the brecciated eucrite meteorites.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003PhyA..328..449D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003PhyA..328..449D"><span>From <span class="hlt">phase</span> <span class="hlt">separation</span> to long-range order in a system of interacting electrons</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Derzhko, Volodymyr; Jȩdrzejewski, Janusz</p> <p>2003-10-01</p> <p>We study a system composed of fermions (electrons), hopping on a square lattice, and of immobile particles (ions), that is described by the spinless Falicov-Kimball Hamiltonian augmented by a next-nearest-neighbor attractive interaction between the ions (a nearest-neighbor repulsive interaction between the ions can be included and does not alter the results). A part of the grand-canonical <span class="hlt">phase</span> diagram of this system is constructed rigorously, when the coupling between the electrons and ions is much stronger than the hopping intensity of electrons. The obtained diagram implies that, at least for a few rational densities of particles, by increasing the hopping intensity the system can be driven from a state of <span class="hlt">phase</span> <span class="hlt">separation</span> to a state with a long-range order. This kind of transitions occurs also, when the hopping fermions are replaced by hopping hard-core bosons.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004OptRv..11..349M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004OptRv..11..349M"><span>Light Diffraction of Aligned Polymer Fibers Periodically Dispersed by <span class="hlt">Phase</span> <span class="hlt">Separation</span> of Liquid Crystal and Polymer</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Murashige, Takeshi; Fujikake, Hideo; Sato, Hiroto; Kikuchi, Hiroshi; Kurita, Taiichiro; Sato, Fumio</p> <p>2004-12-01</p> <p>We have confirmed light diffraction of aligned polymer fibers obtained by a <span class="hlt">phase</span> <span class="hlt">separation</span> of an anisotropic-<span class="hlt">phase</span> solution of liquid crystal and polymer. He—Ne laser light passing through the polymer fibers was scattered in the axis vertical to the fibers, and had two peaks of light intensity symmetrical to the center of the transmitting laser spot. The two peaks were found to be caused by light diffraction due to the periodic polymer-fiber dispersion because the peaks corresponded to values calculated by intervals between the fibers. The periodical fiber networks are considered to be formed by anisotropic spinodal decomposition. This effect can be used to measure the dispersion order of the polymer fibers.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24978241','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24978241"><span>Optical <span class="hlt">phase</span> locking of two infrared continuous wave lasers <span class="hlt">separated</span> by 100  THz.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chiodo, N; Du-Burck, F; Hrabina, J; Lours, M; Chea, E; Acef, O</p> <p>2014-05-15</p> <p>We report on <span class="hlt">phase</span> locking of two continuous wave IR laser sources <span class="hlt">separated</span> by 100 THz emitting around 1029 and 1544 nm, respectively. Our approach uses three independent harmonic generation processes of the IR laser frequencies in periodically poled MgO:LiNbO3 crystals to generate second and third harmonics of those two IR sources. The beat note between the two independent green radiations generated around 515 nm is used to <span class="hlt">phase</span> lock one IR laser to the other, with tunable radio frequency offset. In this way, the whole setup operates as a mini-frequency comb emitting four intense optical radiations (1544, 1029, 772, and 515 nm), with output powers at least three orders of magnitude higher than the available power from each mode emitted by femtosecond lasers.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/21471207','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/21471207"><span>EXOPLANET ALBEDO SPECTRA AND COLORS AS A FUNCTION OF PLANET <span class="hlt">PHASE</span>, <span class="hlt">SEPARATION</span>, AND METALLICITY</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Cahoy, Kerri L.; Marley, Mark S.; Fortney, Jonathan J.</p> <p>2010-11-20</p> <p>First generation space-based optical coronagraphic telescopes will obtain images of cool gas- and ice-giant exoplanets around nearby stars. Exoplanets lying at planet-star <span class="hlt">separations</span> larger than about 1 AU-where an exoplanet can be resolved from its parent star-have spectra that are dominated by reflected light to beyond 1 {mu}m and punctuated by molecular absorption features. Here, we consider how exoplanet albedo spectra and colors vary as a function of planet-star <span class="hlt">separation</span>, metallicity, mass, and observed <span class="hlt">phase</span> for Jupiter and Neptune analogs from 0.35 to 1 {mu}m. We model Jupiter analogs with 1x and 3x the solar abundance of heavy elements, and Neptune analogs with 10x and 30x the solar abundance of heavy elements. Our model planets orbit a solar analog parent star at <span class="hlt">separations</span> of 0.8 AU, 2 AU, 5 AU, and 10 AU. We use a radiative-convective model to compute temperature-pressure profiles. The giant exoplanets are found to be cloud-free at 0.8 AU, possess H{sub 2}O clouds at 2 AU, and have both NH{sub 3} and H{sub 2}O clouds at 5 AU and 10 AU. For each model planet we compute moderate resolution (R = {lambda}/{Delta}{lambda} {approx} 800) albedo spectra as a function of <span class="hlt">phase</span>. We also consider low-resolution spectra and colors that are more consistent with the capabilities of early direct imaging capabilities. As expected, the presence and vertical structure of clouds strongly influence the albedo spectra since cloud particles not only affect optical depth but also have highly directional scattering properties. Observations at different <span class="hlt">phases</span> also probe different volumes of atmosphere as the source-observer geometry changes. Because the images of the planets themselves will be unresolved, their <span class="hlt">phase</span> will not necessarily be immediately obvious, and multiple observations will be needed to discriminate between the effects of planet-star <span class="hlt">separation</span>, metallicity, and <span class="hlt">phase</span> on the observed albedo spectra. We consider the range of these combined effects on</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/6182175','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/6182175"><span><span class="hlt">Separation</span> studies of As(III), Sb(III) and Bi(III) by reversed-<span class="hlt">phase</span> paper chromatographic technique</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Raman, B.; Shinde, V.M.</p> <p>1987-07-01</p> <p>Reversed-<span class="hlt">phase</span> paper chromatographic <span class="hlt">separations</span> of As(III), Sb(III) and Bi(III) have been carried out on Whatman No 1 filter paper impregnated with triphenylphosphine oxide as stationary <span class="hlt">phase</span> and using organic complexing agents such as sodium acetate, sodium succinate and sodium malonate solutions as active mobile <span class="hlt">phases</span>. Results for the <span class="hlt">separation</span> of binary and ternary mixtures are reported and the method has been successfully applied to the <span class="hlt">separation</span> and detection of these elements present in real samples and at ppm level concentration.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22330132','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22330132"><span>Aqueous <span class="hlt">phase</span> <span class="hlt">separation</span> as a possible route to compartmentalization of biological molecules.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Keating, Christine D</p> <p>2012-12-18</p> <p>How could the incredible complexity of modern cells evolve from something simple enough to have appeared in a primordial soup? This enduring question has sparked the interest of researchers since Darwin first considered his theory of natural selection. Organic molecules, even potentially functional molecules including peptides and nucleotides, can be produced abiotically. Amphiphiles such as surfactants and lipids display remarkable self-assembly processes including the spontaneous formation of vesicles resembling the membranes of living cells. Nonetheless, numerous questions remain. Given the presumably dilute concentrations of macromolecules in the prebiotic pools where the earliest cells are thought to have appeared, how could the necessary components become concentrated and encapsulated within a semipermeable membrane? What would drive the further structural complexity that is a hallmark of modern living systems? The interior of modern cells is subdivided into microcompartments such as the nucleoid of bacteria or the organelles of eukaryotic cells. Even within what at first appears to be a single compartment, for example, the cytoplasm or nucleus, chemical composition is often nonuniform, containing gradients, macromolecular assemblies, and/or liquid droplets. What might the internal structure of intermediate evolutionary forms have looked like? The nonideal aqueous solution chemistry of macromolecules offers an attractive possible answer to these questions. Aqueous polymer solutions will form multiple coexisting thermodynamic <span class="hlt">phases</span> under a variety of readily accessible conditions. In this Account, we describe aqueous <span class="hlt">phase</span> <span class="hlt">separation</span> as a model system for biological compartmentalization in both early and modern cells, with an emphasis on systems that have been encapsulated within a lipid bilayer. We begin with an introduction to aqueous <span class="hlt">phase</span> <span class="hlt">separation</span> and discuss how this phenomenon can lead to microcompartmentalization and could facilitate biopolymer</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3525015','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3525015"><span>Aqueous <span class="hlt">Phase</span> <span class="hlt">Separation</span> as a Possible Route to Compartmentalization of Biological Molecules</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p></p> <p>2012-01-01</p> <p>How could the incredible complexity of modern cells evolve from something simple enough to have appeared in a primordial soup? This enduring question has sparked the interest of researchers since Darwin first considered his theory of natural selection. Organic molecules, even potentially functional molecules including peptides and nucleotides, can be produced abiotically. Amphiphiles such as surfactants and lipids display remarkable self-assembly processes including the spontaneous formation of vesicles resembling the membranes of living cells. Nonetheless, numerous questions remain. Given the presumably dilute concentrations of macromolecules in the prebiotic pools where the earliest cells are thought to have appeared, how could the necessary components become concentrated and encapsulated within a semipermeable membrane? What would drive the further structural complexity that is a hallmark of modern living systems? The interior of modern cells is subdivided into microcompartments such as the nucleoid of bacteria or the organelles of eukaryotic cells. Even within what at first appears to be a single compartment, for example, the cytoplasm or nucleus, chemical composition is often nonuniform, containing gradients, macromolecular assemblies, and/or liquid droplets. What might the internal structure of intermediate evolutionary forms have looked like? The nonideal aqueous solution chemistry of macromolecules offers an attractive possible answer to these questions. Aqueous polymer solutions will form multiple coexisting thermodynamic <span class="hlt">phases</span> under a variety of readily accessible conditions. In this Account, we describe aqueous <span class="hlt">phase</span> <span class="hlt">separation</span> as a model system for biological compartmentalization in both early and modern cells, with an emphasis on systems that have been encapsulated within a lipid bilayer. We begin with an introduction to aqueous <span class="hlt">phase</span> <span class="hlt">separation</span> and discuss how this phenomenon can lead to microcompartmentalization and could facilitate biopolymer</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AIPC.1683b0005A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AIPC.1683b0005A"><span><span class="hlt">Thermotropic</span> nanostructured "gel in gel" systems for improved oil recovery and water shutoff</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Altunina, L. K.; Kuvshinov, V. A.; Stasyeva, L. A.</p> <p>2015-10-01</p> <p><span class="hlt">Thermotropic</span> nanostructured system with two gel-forming components has been created based on inorganic hydroxypolymer and organic polymer with a lower critical solution temperature of "aluminum salt-cellulose ether-carbamide-water", forming at heating a bound-dispersed nano-sized "gel in gel" structure. The studies on the kinetics of gelation and rheological properties of solutions and gels in this system have shown that the gels have a higher viscosity and elasticity and thereby are promising for creating deflecting screens in oil reservoirs, redistribution of filtration flows, improved oil recovery and for water shutoff.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016ApPhL.109j3702V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016ApPhL.109j3702V"><span>Investigating <span class="hlt">phase</span> <span class="hlt">separation</span> and structural coloration of self-assembled ternary polymer thin films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Vohra, Varun; Galeotti, Francesco; Giovanella, Umberto; Anzai, Takuya; Kozma, Erika; Botta, Chiara</p> <p>2016-09-01</p> <p>Poly(3-hexylthiophene-2,5-diyl) (P3HT) can generate nanoporous structures with variable pore diameters ranging from 150 to 600 nm from spin-coated blends with polystyrene (PS). In the present study, we observe the effect of the addition of polymethylmethacrylate (PMMA) to P3HT:PS blends to increase the pore-to-pore dimensions up to the micrometer scale. The <span class="hlt">phase</span> <span class="hlt">separation</span> in the ternary blend can be directly visualized by replacing the commercial (non-emissive) PS with a boron-dipyrromethene functionalized PS to distinctively locate the red-emitting P3HT and the green-emitting PS <span class="hlt">phases</span>. In particular, in the ternary blend with high PMMA contents, we observe that PS acts as a compatibilizing agent at the interface between the P3HT and PMMA <span class="hlt">phases</span>. After selective removal of the PS and PMMA <span class="hlt">phases</span> using acetone, we demonstrate that, in these P3HT structured thin films, iridescence can be observed as they exhibit angle dependent reflectivity which is further emphasized when covered with a thin metal layer. The metal covered nanostructured P3HT films display bright color switching properties with blue and red emission at low and high reflection angles, respectively.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4764927','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4764927"><span>Direct single-shot <span class="hlt">phase</span> retrieval from the diffraction pattern of <span class="hlt">separated</span> objects</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Leshem, Ben; Xu, Rui; Dallal, Yehonatan; Miao, Jianwei; Nadler, Boaz; Oron, Dan; Dudovich, Nirit; Raz, Oren</p> <p>2016-01-01</p> <p>The non-crystallographic <span class="hlt">phase</span> problem arises in numerous scientific and technological fields. An important application is coherent diffractive imaging. Recent advances in X-ray free-electron lasers allow capturing of the diffraction pattern from a single nanoparticle before it disintegrates, in so-called ‘diffraction before destruction' experiments. Presently, the <span class="hlt">phase</span> is reconstructed by iterative algorithms, imposing a non-convex computational challenge, or by Fourier holography, requiring a well-characterized reference field. Here we present a convex scheme for single-shot <span class="hlt">phase</span> retrieval for two (or more) sufficiently <span class="hlt">separated</span> objects, demonstrated in two dimensions. In our approach, the objects serve as unknown references to one another, reducing the <span class="hlt">phase</span> problem to a solvable set of linear equations. We establish our method numerically and experimentally in the optical domain and demonstrate a proof-of-principle single-shot coherent diffractive imaging using X-ray free-electron lasers pulses. Our scheme alleviates several limitations of current methods, offering a new pathway towards direct reconstruction of complex objects. PMID:26899582</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.osti.gov/scitech/servlets/purl/1253376','SCIGOV-STC'); return false;" href="http://www.osti.gov/scitech/servlets/purl/1253376"><span>Direct single-shot <span class="hlt">phase</span> retrieval from the diffraction pattern of <span class="hlt">separated</span> objects</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Leshem, Ben; Xu, Rui; Dallal, Yehonatan; Miao, Jianwei; Nadler, Boaz; Oron, Dan; Dudovich, Nirit; Raz, Oren</p> <p>2016-02-22</p> <p>The non-crystallographic <span class="hlt">phase</span> problem arises in numerous scientific and technological fields. An important application is coherent diffractive imaging. Recent advances in X-ray free-electron lasers allow capturing of the diffraction pattern from a single nanoparticle before it disintegrates, in so-called ‘diffraction before destruction’ experiments. Presently, the <span class="hlt">phase</span> is reconstructed by iterative algorithms, imposing a non-convex computational challenge, or by Fourier holography, requiring a well-characterized reference field. Here we present a convex scheme for single-shot <span class="hlt">phase</span> retrieval for two (or more) sufficiently <span class="hlt">separated</span> objects, demonstrated in two dimensions. In our approach, the objects serve as unknown references to one another, reducing the <span class="hlt">phase</span> problem to a solvable set of linear equations. We establish our method numerically and experimentally in the optical domain and demonstrate a proof-of-principle single-shot coherent diffractive imaging using X-ray free-electron lasers pulses. Lastly, our scheme alleviates several limitations of current methods, offering a new pathway towards direct reconstruction of complex objects.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/22489127','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/22489127"><span>Facet-controlled <span class="hlt">phase</span> <span class="hlt">separation</span> in supersaturated Au-Ni nanoparticles upon shape equilibration</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Herz, A. E-mail: dong.wang@tu-ilmenau.de; Rossberg, D.; Hentschel, M.; Theska, F.; Wang, D. E-mail: dong.wang@tu-ilmenau.de; Schaaf, P.; Friák, M.; Holec, D.; Šob, M.; Schneeweiss, O.</p> <p>2015-08-17</p> <p>Solid-state dewetting is used to fabricate supersaturated, submicron-sized Au-Ni solid solution particles out of thin Au/Ni bilayers by means of a rapid thermal annealing technique. <span class="hlt">Phase</span> <span class="hlt">separation</span> in such particles is studied with respect to their equilibrium crystal (or Wulff) shape by subsequent annealing at elevated temperature. It is found that (100) faceting planes of the equilibrated particles are enriched with Ni and (111) faces with Au. Both <span class="hlt">phases</span> are considered by quantum-mechanical calculations in combination with an error-reduction scheme that was developed to compensate for a missing exchange-correlation potential that would reliably describe both Au and Ni. The observed <span class="hlt">phase</span> configuration is then related to the minimization of strongly anisotropic elastic energies of Au- and Ni-rich <span class="hlt">phases</span> and results in a rather unique nanoparticle composite state that is characterized by nearly uniform value of elastic response to epitaxial strains all over the faceted surface. The same conclusion is yielded also by evaluating bi-axial elastic moduli when employing interpolated experimental elastic constants. This work demonstrates a useful route for studying features of physical metallurgy at the mesoscale.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5311949','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5311949"><span>In situ observation of macroscopic <span class="hlt">phase</span> <span class="hlt">separation</span> in cobalt hexacyanoferrate film</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Takachi, Masamitsu; Moritomo, Yutaka</p> <p>2017-01-01</p> <p>Lithium-ion secondary batteries (LIBs) store electric energy via Li+ deintercalation from cathode materials. The Li+ deintercalation frequently drives a first-order <span class="hlt">phase</span> transition of the cathode material as a result of the Li-ordering or Li-concentration effect and causes a <span class="hlt">phase</span> <span class="hlt">separation</span> (PS) into the Li-rich and Li-poor <span class="hlt">phases</span>. Here, we performed an in situ microscopic investigation of the PS dynamics in thin films of cobalt hexacyanoferrate, LixCo[Fe(CN)6]0.9, against Li+ deintercalation. The thick film (d = 1.5 μm) shows a characteristic macroscopic PS of several tens of μm into the green (Li1.6Co[Fe(CN)6]0.9) and black (Li.6Co[Fe(CN)6]0.9) <span class="hlt">phases</span> in the x range of 1.0 < x < 1.6. Reflecting the substrate strain, the thin film (d = 0.5 μm) shows no trace of the PS in the entire x region. Our observation suggests that the macroscopic PS plays a significant role in the charge/discharge dynamics of the cathode. PMID:28205619</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_24 --> <div id="page_25" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="481"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017NatSR...742694T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017NatSR...742694T"><span>In situ observation of macroscopic <span class="hlt">phase</span> <span class="hlt">separation</span> in cobalt hexacyanoferrate film</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Takachi, Masamitsu; Moritomo, Yutaka</p> <p>2017-02-01</p> <p>Lithium-ion secondary batteries (LIBs) store electric energy via Li+ deintercalation from cathode materials. The Li+ deintercalation frequently drives a first-order <span class="hlt">phase</span> transition of the cathode material as a result of the Li-ordering or Li-concentration effect and causes a <span class="hlt">phase</span> <span class="hlt">separation</span> (PS) into the Li-rich and Li-poor <span class="hlt">phases</span>. Here, we performed an in situ microscopic investigation of the PS dynamics in thin films of cobalt hexacyanoferrate, LixCo[Fe(CN)6]0.9, against Li+ deintercalation. The thick film (d = 1.5 μm) shows a characteristic macroscopic PS of several tens of μm into the green (Li1.6Co[Fe(CN)6]0.9) and black (Li.6Co[Fe(CN)6]0.9) <span class="hlt">phases</span> in the x range of 1.0 < x < 1.6. Reflecting the substrate strain, the thin film (d = 0.5 μm) shows no trace of the PS in the entire x region. Our observation suggests that the macroscopic PS plays a significant role in the charge/discharge dynamics of the cathode.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016APS..MARA37003W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016APS..MARA37003W"><span>Mapping Liquid-liquid protein <span class="hlt">phase</span> <span class="hlt">separation</span> using ultra-fast-scanning fluorescence correlation spectroscopy</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wei, Ming-Tzo; Elbaum-Garfinkle, Shana; Arnold, Craig B.; Priestley, Rodney D.; Brangwynne, Clifford P.</p> <p></p> <p>Intrinsically disordered proteins (IDPs) are an understudied class of proteins that play important roles in a wide variety of biological processes in cells. We've previously shown that the C. elegans IDP LAF-1 <span class="hlt">phase</span> <span class="hlt">separates</span> into P granule-like droplets in vitro. However, the physics of the condensed <span class="hlt">phase</span> remains poorly understood. Here, we use a novel technique, ultra-fast-scanning fluorescence correlation spectroscopy, to study the nano-scale rheological properties of LAF-1 droplets. Ultra-fast-scanning FCS uses a tunable acoustic gradient index of refraction (TAG) lens with an oil immersion objective to control axial movement of the focal point over a length of several micrometers at frequencies of 70kHz. Using ultra-fast-scanning FCS allows for the accurate determination of molecular concentrations and their diffusion coefficient, when the particle is passing through an excitation volume. Our work reveals an asymmetric LAF-1 <span class="hlt">phase</span> diagram, and demonstrates that LAF-1 droplets are purely viscous <span class="hlt">phases</span> which are highly tunable by salt concentration.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1253376-direct-single-shot-phase-retrieval-from-diffraction-pattern-separated-objects','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1253376-direct-single-shot-phase-retrieval-from-diffraction-pattern-separated-objects"><span>Direct single-shot <span class="hlt">phase</span> retrieval from the diffraction pattern of <span class="hlt">separated</span> objects</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Leshem, Ben; Xu, Rui; Dallal, Yehonatan; ...</p> <p>2016-02-22</p> <p>The non-crystallographic <span class="hlt">phase</span> problem arises in numerous scientific and technological fields. An important application is coherent diffractive imaging. Recent advances in X-ray free-electron lasers allow capturing of the diffraction pattern from a single nanoparticle before it disintegrates, in so-called ‘diffraction before destruction’ experiments. Presently, the <span class="hlt">phase</span> is reconstructed by iterative algorithms, imposing a non-convex computational challenge, or by Fourier holography, requiring a well-characterized reference field. Here we present a convex scheme for single-shot <span class="hlt">phase</span> retrieval for two (or more) sufficiently <span class="hlt">separated</span> objects, demonstrated in two dimensions. In our approach, the objects serve as unknown references to one another, reducing themore » <span class="hlt">phase</span> problem to a solvable set of linear equations. We establish our method numerically and experimentally in the optical domain and demonstrate a proof-of-principle single-shot coherent diffractive imaging using X-ray free-electron lasers pulses. Lastly, our scheme alleviates several limitations of current methods, offering a new pathway towards direct reconstruction of complex objects.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1301891','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1301891"><span>Nonequilibrium phenomena in the <span class="hlt">phase</span> <span class="hlt">separation</span> of a two-component lipid bilayer.</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>de Almeida, Rodrigo F M; Loura, Luís M S; Fedorov, Aleksandre; Prieto, Manuel</p> <p>2002-01-01</p> <p>Lipid bilayers composed of two phospholipids with significant acyl-chain mismatch behave as nonideal mixtures. Although many of these systems are well characterized from the equilibrium point of view, studies concerning their nonequilibrium dynamics are still rare. The kinetics of lipid demixing (<span class="hlt">phase</span> <span class="hlt">separation</span>) was studied in model membranes (large unilamellar vesicles of 1:1 dilauroylphosphatidylcholine (C(12) acyl chain) and distearoylphosphatidylcholine (C(18) acyl chain)). For this purpose, photophysical techniques (fluorescence intensity, anisotropy, and fluorescence resonance energy transfer) were applied using suitable probes (gel <span class="hlt">phase</span> probe trans-parinaric acid and fluid <span class="hlt">phase</span> probe N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)-dilauroylphosphatidylethanolamine). The nonequilibrium situation was induced by a sudden thermal quench from a one-fluid <span class="hlt">phase</span> equilibrium situation (higher temperature) to the gel/fluid coexistence range (lower temperature). We verified that the attainment of equilibrium is a very slow process (occurs in a time scale of hours), leading to large domains at infinite time. The nonequilibrium structure stabilization is due essentially to temporarily rigidified C(12) chains in the interface between gel/fluid domains, which decrease the interfacial tension by acting as surfactants. The relaxation process becomes faster with the increase of the temperature drop. In addition, heterogeneity is already present in the supposed homogeneous fluid mixture at the higher temperature. PMID:11806924</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28069188','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28069188"><span>Simulation of <span class="hlt">phase</span> <span class="hlt">separation</span> with large component ratio for oil-in-water emulsion in ultrasound field.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Heping; Li, Xiaoguang; Li, Yanggui; Geng, Xingguo</p> <p>2017-05-01</p> <p>This paper presents an exploration for <span class="hlt">separation</span> of oil-in-water and coalescence of oil droplets in ultrasound field via lattice Boltzmann method. Simulations were conducted by the ultrasound traveling and standing waves to enhance oil <span class="hlt">separation</span> and trap oil droplets. The focus was to the effect of ultrasound irradiation on oil-in-water emulsion properties in the standing wave field, such as oil drop radius, morphology and growth kinetics of <span class="hlt">phase</span> <span class="hlt">separation</span>. Ultrasound fields were applied to irradiate the oil-in-water emulsion for getting flocculation of the oil droplets in 420kHz case, and larger dispersed oil droplets and continuous <span class="hlt">phases</span> in 2MHz and 10MHz cases, respectively. The <span class="hlt">separated</span> <span class="hlt">phases</span> started to rise along the direction of sound propagation after several periods. The rising rate of the flocks was significantly greater in ultrasound case than that of oil droplets in the original emulsion, indicating that ultrasound irradiation caused a rapid increase of oil droplet quantity in the progress of the <span class="hlt">separation</span>. The <span class="hlt">separation</span> degree was also significantly improved with increasing frequency or irradiation time. The dataset was rearranged for growth kinetics of ultrasonic <span class="hlt">phase</span> <span class="hlt">separation</span> in a plot by spherically averaged structure factor and the ratio of oil and emulsion <span class="hlt">phases</span>. The analyses recovered the two different temporal regimes: the spinodal decomposition and domain growth stages, which further quantified the morphology results. These numerical results provide guidance for setting the optimum condition for the <span class="hlt">separation</span> of oil-in-water emulsion in the ultrasound field.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21271700','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21271700"><span>3D interconnected ionic nano-channels formed in polymer films: self-organization and polymerization of <span class="hlt">thermotropic</span> bicontinuous cubic liquid crystals.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ichikawa, Takahiro; Yoshio, Masafumi; Hamasaki, Atsushi; Kagimoto, Junko; Ohno, Hiroyuki; Kato, Takashi</p> <p>2011-02-23</p> <p><span class="hlt">Thermotropic</span> bicontinuous cubic (Cub(bi)) liquid-crystalline (LC) compounds based on a polymerizable ammonium moiety complexed with a lithium salt have been designed to obtain lithium ion-conductive all solid polymeric films having 3D interconnected ionic channels. The monomer shows a Cub(bi) <span class="hlt">phase</span> from -5 to 19 °C on heating. The complexes retain the ability to form the Cub(bi) LC <span class="hlt">phase</span>. They also form hexagonal columnar (Col(h)) LC <span class="hlt">phases</span> at temperatures higher than those of the Cub(bi) <span class="hlt">phases</span>. The complex of the monomer and LiBF(4) at the molar ratio of 4:1 exhibits the Cub(bi) and Col(h) <span class="hlt">phases</span> between -6 to 19 °C and 19 to 56 °C, respectively, on heating. The Cub(bi) LC structure formed by the complex has been successfully preserved by in situ photopolymerization through UV irradiation in the presence of a photoinitiator. The resultant nanostructured film is optically transparent and free-standing. The X-ray analysis of the film confirms the preservation of the self-assembled nanostructure. The polymer film with the Cub(bi) LC nanostructure exhibits higher ionic conductivities than the polymer films obtained by photopolymerization of the complex in the Col(h) and isotropic <span class="hlt">phases</span>. It is found that the 3D interconnected ionic channels derived from the Cub(bi) <span class="hlt">phase</span> function as efficient ion-conductive pathways.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23859796','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23859796"><span>Factors influencing the <span class="hlt">separation</span> of oligonucleotides using reversed-<span class="hlt">phase</span>/ion-exchange mixed-mode high performance liquid chromatography columns.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Biba, Mirlinda; Jiang, Eileen; Mao, Bing; Zewge, Daniel; Foley, Joe P; Welch, Christopher J</p> <p>2013-08-23</p> <p>New mixed-mode columns consisting of reversed-<span class="hlt">phase</span> and ion-exchange <span class="hlt">separation</span> modes were evaluated for the analysis of short RNA oligonucleotides (∼20mers). Conventional analysis for these samples typically involves using two complementary methods: strong anion-exchange liquid chromatography (SAX-LC) for <span class="hlt">separation</span> based on charge, and ion-pair reversed-<span class="hlt">phase</span> liquid chromatography (IP-RPLC) for <span class="hlt">separation</span> based on hydrophobicity. Recently introduced mixed-mode high performance liquid chromatography (HPLC) columns combine both reversed-<span class="hlt">phase</span> and ion-exchange modes, potentially offering a simpler analysis by combining the benefits of both <span class="hlt">separation</span> modes into a single method. Analysis of a variety of RNA oligonucleotide samples using three different mixed-mode stationary <span class="hlt">phases</span> showed some distinct benefits for oligonucleotide <span class="hlt">separation</span> and analysis. When using these mixed-mode columns with typical IP-RPLC mobile <span class="hlt">phase</span> conditions, such as ammonium acetate or triethylammonium acetate as the primary ion-pair reagent, the <span class="hlt">separation</span> was mainly based on the IP-RPLC mode. However, when changing the mobile <span class="hlt">phase</span> conditions to those more typical for SAX-LC, such as salt gradients with NaCl or NaBr, very different <span class="hlt">separation</span> patterns were observed due to mixed-mode interactions. In addition, the Scherzo SW-C18 and SM-C18 columns with sodium chloride or sodium bromide salt gradients also showed significant improvements in peak shape.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016GeCoA.183..125S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016GeCoA.183..125S"><span>Fractionation of Cl/Br during fluid <span class="hlt">phase</span> <span class="hlt">separation</span> in magmatic-hydrothermal fluids</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Seo, Jung Hun; Zajacz, Zoltán</p> <p>2016-06-01</p> <p>Brine and vapor inclusions were synthesized to study Cl/Br fractionation during magmatic-hydrothermal fluid <span class="hlt">phase</span> <span class="hlt">separation</span> at 900 °C and pressures of 90, 120, and 150 MPa in Li/Na/K halide salt-H2O systems. Laser ablation ICP-MS microanalysis of high-density brine inclusions show an elevated Cl/Br ratio compared to the coexisting low-density vapor inclusions. The degree of Cl/Br fractionation between vapor and brine is significantly dependent on the identity of the alkali metal in the system: stronger vapor partitioning of Br occurs in the Li halide-H2O system compared to the systems of K and Na halide-H2O. The effect of the identity of alkali-metals in the system is stronger compared to the effect of vapor-brine density contrast. We infer that competition between alkali-halide and alkali-OH complexes in high-temperature fluids might cause the Cl/Br fractionation, consistent with the observed molar imbalances of alkali metals compared to halides in the analyzed brine inclusions. Our experiments show that the identity of alkali metals controls the degrees of Cl/Br fractionation between the <span class="hlt">separating</span> aqueous fluid <span class="hlt">phases</span> at 900 °C, and suggest that a significant variability in the Cl/Br ratios of magmatic fluids can arise in Li-rich systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25063098','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25063098"><span>A novel bio-safe <span class="hlt">phase</span> <span class="hlt">separation</span> process for preparing open-pore biodegradable polycaprolactone microparticles.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Salerno, Aurelio; Domingo, Concepción</p> <p>2014-09-01</p> <p>Open-pore biodegradable microparticles are object of considerable interest for biomedical applications, particularly as cell and drug delivery carriers in tissue engineering and health care treatments. Furthermore, the engineering of microparticles with well definite size distribution and pore architecture by bio-safe fabrication routes is crucial to avoid the use of toxic compounds potentially harmful to cells and biological tissues. To achieve this important issue, in the present study a straightforward and bio-safe approach for fabricating porous biodegradable microparticles with controlled morphological and structural features down to the nanometer scale is developed. In particular, ethyl lactate is used as a non-toxic solvent for polycaprolactone particles fabrication via a thermal induced <span class="hlt">phase</span> <span class="hlt">separation</span> technique. The used approach allows achieving open-pore particles with mean particle size in the 150-250 μm range and a 3.5-7.9 m(2)/g specific surface area. Finally, the combination of thermal induced <span class="hlt">phase</span> <span class="hlt">separation</span> and porogen leaching techniques is employed for the first time to obtain multi-scaled porous microparticles with large external and internal pore sizes and potential improved characteristics for cell culture and tissue engineering. Samples were characterized to assess their thermal properties, morphology and crystalline structure features and textural properties.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27482542','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27482542"><span>Self-optimized superconductivity attainable by interlayer <span class="hlt">phase</span> <span class="hlt">separation</span> at cuprate interfaces.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Misawa, Takahiro; Nomura, Yusuke; Biermann, Silke; Imada, Masatoshi</p> <p>2016-07-01</p> <p>Stabilizing superconductivity at high temperatures and elucidating its mechanism have long been major challenges of materials research in condensed matter physics. Meanwhile, recent progress in nanostructuring offers unprecedented possibilities for designing novel functionalities. Above all, thin films of cuprate and iron-based high-temperature superconductors exhibit remarkably better superconducting characteristics (for example, higher critical temperatures) than in the bulk, but the underlying mechanism is still not understood. Solving microscopic models suitable for cuprates, we demonstrate that, at an interface between a Mott insulator and an overdoped nonsuperconducting metal, the superconducting amplitude is always pinned at the optimum achieved in the bulk, independently of the carrier concentration in the metal. This is in contrast to the dome-like dependence in bulk superconductors but consistent with the astonishing independence of the critical temperature from the carrier density x observed at the interfaces of La2CuO4 and La2-x Sr x CuO4. Furthermore, we identify a self-organization mechanism as responsible for the pinning at the optimum amplitude: An emergent electronic structure induced by interlayer <span class="hlt">phase</span> <span class="hlt">separation</span> eludes bulk <span class="hlt">phase</span> <span class="hlt">separation</span> and inhomogeneities that would kill superconductivity in the bulk. Thus, interfaces provide an ideal tool to enhance and stabilize superconductivity. This interfacial example opens up further ways of shaping superconductivity by suppressing competing instabilities, with direct perspectives for designing devices.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007APS..MARU24001H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007APS..MARU24001H"><span>Influence of <span class="hlt">Phase</span> <span class="hlt">Separation</span> and Shear on the Crystallization of Polyolefin Blends</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Han, Charles C.</p> <p>2007-03-01</p> <p>The correlation between liquid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> (LLPS) and crystallization at several compositions in statistical copolymer blends of poly (ethylene-co-hexene) (PEH) and poly (ethylene-co-butene) (PEB) has been examined by optical microscopy (OM), atomic force microscopy (AFM) and differential scanning calorimetry (DSC). The overwhelming change in the crystallization kinetics due to the density fluctuation caused by the spontaneous spinodal LLPS is observed. This coupling mechanism suggests a new mechanism in the nucleation-crystallization process. All evidences are pointing to a cross-over mechanism from the spinodal fluctuations (of liquid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span>) to the nucleation and than crystallization. Also, the shear dependence and mechanism of the Shih-kebab formation in the isotactic polypropylene (iPP) and isotactic polypropylene/polyethylene-co-octene blends have been studied. The network strands deformation and the primary nucleation mechanism have been studied by the time resolved small angle light scattering and AFM. New mechanism has been proposed. The above studies are aimed to understand the enhanced primary nucleation mechanisms in crystallizable polymers and polymer blends which have not been emphasized in most of the traditional nucleation and crystallization research in polymers. The detailed experimental evidences and proposed physical model will be presented.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003PhyA..319...56K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003PhyA..319...56K"><span>Thermally induced coupling of <span class="hlt">phase</span> <span class="hlt">separation</span> and gelation in an aqueous solution of hydroxypropylmethylcellulose (HPMC)</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kita, Rio; Kaku, Takeshi; Ohashi, Hitoshi; Kurosu, Tateki; Iida, Masamori; Yagihara, Shin; Dobashi, Toshiaki</p> <p>2003-03-01</p> <p>Thermally induced coupling of gelation and <span class="hlt">phase</span> <span class="hlt">separation</span> in polysaccharide aqueous solutions has a complex feature because of critical and tricritical phenomena, thermally induced hydrophobic interaction, and molecular-weight distribution of the polysaccharide. To elucidate the process, the criticality of a hydroxypropylmethylcellulose (HPMC) aqueous solution was assessed, and then dielectric relaxation and fluorescence intensity experiments were carried out. The diffusion coefficient of the solution with a weight fraction of HPMC being 0.06 could be extrapolated to zero at the cloud-point curve which showed the criticality of the solution. The fluorescence intensity increased at a temperature much lower than the cloud point and the gel point, especially for concentrated solutions, indicating the hydrophobic interaction as the driving force of the gelation coupled by the <span class="hlt">phase</span> <span class="hlt">separation</span>. Dielectric relaxation measurements by time-domain reflectometry revealed two characteristic relaxations of chain motions around 100 MHz and orientation of free water around 20 GHz, which is accompanied by a low-frequency tail reflecting hydration water.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19750009113','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19750009113"><span>Thermodynamics and <span class="hlt">phase</span> <span class="hlt">separation</span> of dense fully-ionized hydrogen-helium fluid mixtures</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Stevenson, D. J.</p> <p>1975-01-01</p> <p>The free energy of a hydrogen-helium fluid mixture is evaluated for the temperatures and densities appropriate to the deep interior of a giant planet such as Jupiter. The electrons are assumed to be fully pressure-ionized and degenerate. In this regime, an appropriate first approximation to the ionic distribution functions can be found by assuming hard sphere interactions. Corrections to this approximation are incorporated by means of the perturbation theory of Anderson and Chandler. Approximations for the three-body interactions and the nonlinear response of the electron gas to the ions are included. It is predicted that a hydrogen-helium mixture, containing 10% by number of helium ions, <span class="hlt">separates</span> into hydrogen-rich and helium-rich <span class="hlt">phases</span> below about 8000 K, at the pressures relevant to Jupiter (4-40 Megabars). It is also predicted that the alloy occupies less volume per ion than the <span class="hlt">separated</span> <span class="hlt">phases</span>. The equations of state and other thermodynamic derivatives are tabulated. Implications of these results are discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22678989','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22678989"><span>Construction of macroscopic cytomimetic vesicle aggregates based on click chemistry: controllable vesicle fusion and <span class="hlt">phase</span> <span class="hlt">separation</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Jin, Haibao; Huang, Wei; Zheng, Yongli; Zhou, Yongfeng; Yan, Deyue</p> <p>2012-07-09</p> <p>Vesicle-vesicle aggregation to mimic cell-cell aggregation has attracted much attention. Here, hyperbranched polymer vesicles (branched-polymersomes, BPs) with a cell-like size were selected as model membranes, and the vesicle aggregation process, triggered by click chemistry of the copper-catalysed azide-alkyne cycloaddition reaction, was systematically studied. For this purpose, azide and alkynyl groups were loaded on the membranes of BPs through the co-assembly method to obtain N(3)-BPs and Alk-BPs, respectively. Subsequently, macroscopic vesicle aggregates were obtained when these two kinds of functional BPs were mixed together with the ratio of azide to alkynyl groups of about 1:1. Both the vesicle fusion events and lateral <span class="hlt">phase</span> <span class="hlt">separation</span> on the vesicle membrane occurred during such a vesicle aggregation process, and the fusion rate and <span class="hlt">phase-separation</span> degree could be controlled by adjusting the clickable group content. The vesicle aggregation process with N(3) -micelles as desmosome mimics to connect with Alk-BPs through click-chemistry reaction was also studied, and large-scale vesicle aggregates without vesicle fusion were obtained in this process. The present work has extended the controllable cytomimetic vesicle aggregation process with the use of covalent bonds, instead of noncovalent bonds, as the driving force.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007SPIE.6656E..0PH','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007SPIE.6656E..0PH"><span>Interface control in organic heterojunction photovoltaic cells by <span class="hlt">phase</span> <span class="hlt">separation</span> processes</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Heier, Jakob; Castro, Fernando A.; Nüesch, Frank; Hany, Roland</p> <p>2007-09-01</p> <p>Significant progress is being made in the photovoltaic energy conversion using organic semiconducting materials. One of the focuses of attention is the nanoscale morphology of the donor-acceptor mixture, to ensure efficient charge generation and loss-free charge transport at the same time. Using small molecule and polymer blend systems, recent efforts highlight the problems to ensure an optimized relationship between molecular structure, morphology and device properties. Here, we present two examples using a host/guest mixture approach for the controlled, sequential design of bilayer organic solar cell architectures that consist of a large interface area with connecting paths to the respective electrodes at the same time. In the first example, we employed polymer demixing during spin coating to produce a rough interface: surface directed spinodal decomposition leads to a 2-dimensional spinodal pattern with submicrometer features at the polymer-polymer interface. The second system consists of a solution of a blend of small molecules, where <span class="hlt">phase</span> <span class="hlt">separation</span> into a bilayer during spin coating is followed by dewetting. For both cases, the guest can be removed using a selective solvent after the <span class="hlt">phase</span> <span class="hlt">separation</span> process, and the rough host surface can be covered with a second active, semiconducting component. We explain the potential merits of the resulting interdigitated bilayer films, and explore to which extent polymer-polymer and surface interactions can be employed to create surface features in the nanometer range.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/141292','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/141292"><span>Characterization and <span class="hlt">separation</span> of ash from CANMET coprocessing residue by oil <span class="hlt">phase</span> agglomeration techniques</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Majid, A.; Coleman, R.D.; Toll, R.; Pleizier, G.; Deslandes, Y.; Sparks, B.D.; Ikura, M.</p> <p>1993-12-31</p> <p>CANMET`s coal/heavy oil coprocessing unit yields a solid residue that contains most of the ash originally associated with the feed coal as well as reacted catalyst solids. Removal of these ash solids would make it possible to recycle the material to extinction, thereby increasing production of lighter oils. In this investigation the authors have used surface characterization techniques such as Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Analysis (EDXA) and X-ray Photoelectron Spectroscopy (XPS) to characterize toluene insoluble solids associated with the pitch residue, in order to evaluate the <span class="hlt">separation</span> potential using oil <span class="hlt">phase</span> agglomeration techniques. Washability studies using float-sink tests were also carried out to determine empirically the level of ash <span class="hlt">separation</span> attainable. Based on the results of these studies several tests were carried out to beneficiate the organic matter in the residue pitch, by using liquid <span class="hlt">phase</span> agglomeration techniques. Levels of ash rejection in these tests ranged from 20% to 40%. SEM and EDXA analysis of the agglomerated product and the reject material and Inductively Coupled Plasma (ICP) analysis of the ash from both materials suggest that most of the iron from added catalyst is retained in the agglomerates.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004JChPh.12011864R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004JChPh.12011864R"><span>Confinement effect on the adsorption from a binary liquid system near liquid/liquid <span class="hlt">phase</span> <span class="hlt">separation</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rother, Gernot; Woywod, Dirk; Schoen, Martin; Findenegg, Gerhard H.</p> <p>2004-06-01</p> <p>The preferential adsorption of one component of a binary system at the inner surfaces of mesoporous silica glasses was studied in a wide composition range at temperatures close to liquid/liquid <span class="hlt">phase</span> <span class="hlt">separation</span>. Confinement effects on the adsorption were investigated by using three controlled-pore glass (CPG-10) materials of different mean pore size (10 to 50 nm). For the experimental system (2-butoxyethanol+water), which exhibits an upper miscibility gap, strong preferential adsorption of water occurs, as the coexistence curve is approached at bulk compositions, at which water is the minority component. In this strong adsorption regime the area-related surface excess amount of adsorbed water decreases with decreasing pore width, while the shift in the volume-related mean composition of the pore liquid shows an opposite trend, i.e., greatest deviation from bulk composition occurring in the most narrow pores. A simple mean-field lattice model of a liquid mixture confined by parallel walls is adopted to rationalize these experimental findings. This model reproduces the main findings of the confinement effect on the adsorption near liquid/liquid <span class="hlt">phase</span> <span class="hlt">separation</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17636998','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17636998"><span>Motion of integrated CdS nanoparticles by <span class="hlt">phase</span> <span class="hlt">separation</span> of block copolymer brushes.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yu, Kai; Wang, Hanfu; Han, Yanchun</p> <p>2007-08-14</p> <p>A new method of reversibly moving CdS nanoparticles in the perpendicular direction was developed on the basis of the <span class="hlt">phase</span> <span class="hlt">separation</span> of block copolymer brushes. Polystyrene-b-(poly(methyl methacrylate)-co-poly(cadmium dimethacrylate)) (PS-b-(PMMA-co-PCdMA)) brushes were grafted from the silicon wafer by surface-initiated atom transfer radical polymerization (ATRP). By exposing the polymer brushes to H2S gas, PS-b-(PMMA-co-PCdMA) brushes were converted to polystyrene-b-(poly(methyl methacrylate)-co-poly(methacrylic acid)(CdS)) (PS-b-(PMMA-co-PMAA(CdS))) brushes, in which CdS nanoparticles were chemically bonded by the carboxylic groups of PMAA segment. Alternating treatment of the PS-b-(PMMA-co-PMAA(CdS)) brushes by selective solvents for the outer block (a mixed solvent of acetone and ethanol) and the inner PS block (toluene) induced perpendicular <span class="hlt">phase</span> <span class="hlt">separation</span> of polymer brushes, which resulted in the reversible lifting and lowering of CdS nanoparticles in the perpendicular direction. The extent of movement can be adjusted by the relative thickness of two blocks of the polymer brushes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2998619','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2998619"><span>Liquid-Liquid <span class="hlt">Phase</span> <span class="hlt">Separation</span> of a Monoclonal Antibody and Nonmonotonic Influence of Hofmeister Anions</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Mason, Bruce D.; Zhang-van Enk, Jian; Zhang, Le; Remmele, Richard L.; Zhang, Jifeng</p> <p>2010-01-01</p> <p>Liquid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> was studied for a monoclonal antibody in the monovalent salt solutions of KF, KCl, and KSCN under different pH conditions. A modified Carnahan-Starling hard-sphere model was utilized to fit the experimental data, establish the liquid-liquid coexistence curve, and determine antibody-antibody interactions in the form of Tc (critical temperature) under the different solution conditions. The liquid-liquid <span class="hlt">phase</span> <span class="hlt">separation</span> revealed the complex relationships between antibody-antibody interactions and different solution conditions, such as pH, ionic strength, and the type of anion. At pH 7.1, close to the pI of the antibody, a decrease of Tc versus ionic strength was observed at low salt conditions, suggesting that the protein-protein interactions became less attractive. At a pH value below the pI of the antibody, a nonmonotonic relationship of Tc versus ionic strength was apparent: initially as the ionic strength increased, protein-protein interactions became more attractive with the effectiveness of the anions following the inverse Hofmeister series; then the interactions became less attractive following the direct Hofmeister series. This nonmonotonic relationship may be explained by combining the charge neutralization by the anions, perhaps with the ion-correlation force for polarizable anions, and their preferential interactions with the antibody. PMID:21112304</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/scitech/biblio/22398920','SCIGOV-STC'); return false;" href="https://www.osti.gov/scitech/biblio/22398920"><span>Spontaneous <span class="hlt">phase</span> <span class="hlt">separation</span> during self-assembly in bi-dispersed spherical iron oxide nanoparticle monolayers</span></a></p> <p><a target="_blank" href="http://www.osti.gov/scitech">SciTech Connect</a></p> <p>Stanley, Jacob; Boucheron, Leandra; Shpyrko, Oleg E-mail: oshpyrko@physics.ucsd.edu; Lin, Binhua E-mail: oshpyrko@physics.ucsd.edu; Meron, Mati</p> <p>2015-04-20</p> <p>Recent developments in the synthesis of iron oxide nanoparticles have resulted in the ability to fabricate roughly spherical particles with extremely high size uniformity (low polydispersity). These particles can form self-assembled monolayer films at an air-water interface. When the polydispersity of the particles is low, these monolayers can be well-ordered over a length scale dozens of times the particle size. The van der Waals force between the particles is what drives this self-assembly. Through the use of Grazing Incidence X-Ray Diffraction we demonstrate that, when these films are formed at the liquid surface from bi-dispersed solutions containing 10 and 20 nm spherical particles suspended in chloroform, the particles <span class="hlt">phase</span> <span class="hlt">separate</span> into well-ordered patches during the self-assembly process. Furthermore, the domain sizes of these <span class="hlt">phase</span> <span class="hlt">separated</span> regions are at most 2–3 times smaller than that of a film comprising only mono-dispersed particles and their degree of disorder is comparable. This is shown for multiple solutions with differing ratios of 10 and 20 nm particles.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_25 --> <center> <div class="footer-extlink text-muted"><small>Some links on this page may take you to non-federal websites. 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