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Sample records for solide-liquide application aux

  1. Atomistic simulation of solid-liquid coexistence for molecular systems: Application to triazole and benzene

    NASA Astrophysics Data System (ADS)

    Eike, David M.; Maginn, Edward J.

    2006-04-01

    A method recently developed to rigorously determine solid-liquid equilibrium using a free-energy-based analysis has been extended to analyze multiatom molecular systems. This method is based on using a pseudosupercritical transformation path to reversibly transform between solid and liquid phases. Integration along this path yields the free energy difference at a single state point, which can then be used to determine the free energy difference as a function of temperature and therefore locate the coexistence temperature at a fixed pressure. The primary extension reported here is the introduction of an external potential field capable of inducing center of mass order along with secondary orientational order for molecules. The method is used to calculate the melting point of 1-H-1,2,4-triazole and benzene. Despite the fact that the triazole model gives accurate bulk densities for the liquid and crystal phases, it is found to do a poor job of reproducing the experimental crystal structure and heat of fusion. Consequently, it yields a melting point that is 100K lower than the experimental value. On the other hand, the benzene model has been parametrized extensively to match a wide range of properties and yields a melting point that is only 20K lower than the experimental value. Previous work in which a simple "direct heating" method was used actually found that the melting point of the benzene model was 50K higher than the experimental value. This demonstrates the importance of using proper free energy methods to compute phase behavior. It also shows that the melting point is a very sensitive measure of force field quality that should be considered in parametrization efforts. The method described here provides a relatively simple approach for computing melting points of molecular systems.

  2. Les ADAF : Application aux binaires X

    NASA Astrophysics Data System (ADS)

    Olive, Jean-Francois

    2001-01-01

    Based on the fundamental review by Narayan et al. (1998), this lecture for the ``23ieme Ecole du CNRS de Goutelas'' on binary systems describes the properties of advection-dominated accretion flows (ADAFs) and their applications to black hole X-ray binaries. The possibility of using ADAFs to explore the event horizons of black holes is highlighted.

  3. Application de la combustion catalytique aux turbines à gaz

    NASA Astrophysics Data System (ADS)

    Lebas, E.; Martin, G. H.

    2002-04-01

    La réduction des émissions d'oxydes d'azote sur turbines à gaz est obtenue par diminution de la température au sein de la chambre de combustion. Les techniques possibles comprennent l'injection d'eau ou de vapeur, la combustion pauvre et l'oxydation catalytique. Parmi celles-ci, la dernière est la plus prometteuse en terme de coûts et de performances, avec des émissions de NOx ramenées à un seul chiffre (typiquement inférieures à 3 ppm). L'IFP travaille depuis maintenant 10 ans sur l'adaptation de la combustion catalytique aux turbines à gaz. Les études ont été conduites au travers de projets européen tels que AGATA (Advance Gas Turbine for Automotive Application) et ULECAT (Ultra Low CATalytic combustor for dual fuel gas turbine). Le premier projet était destiné au développement de véhicules hybrides et le second à la combustion stationnaire de biogaz et de combustible Diesel. Les études en cours dans ce domaine portent sur le développement d'une unité de cogénération intégrant une microturbine à combustion catalytique. Les travaux menés à l'IFP concernent la mise au point de catalyseurs répondant aux exigences de la combustion catalytique en turbine à gaz et le développement de chambres de combustion permettant la mise en oeuvre de ces catalyseurs.

  4. CRYOCHEM, Thermodynamic Model for Cryogenic Chemical Systems: Solid-Vapor and Solid-Liquid-Vapor Phase Equilibria Toward Applications on Titan and Pluto

    NASA Astrophysics Data System (ADS)

    Tan, S. P.; Kargel, J. S.; Adidharma, H.; Marion, G. M.

    2014-12-01

    Until in-situ measurements can be made regularly on extraterrestrial bodies, thermodynamic models are the only tools to investigate the properties and behavior of chemical systems on those bodies. The resulting findings are often critical in describing physicochemical processes in the atmosphere, surface, and subsurface in planetary geochemistry and climate studies. The extremely cold conditions on Triton, Pluto and other Kuiper Belt Objects, and Titan introduce huge non-ideality that prevents conventional models from performing adequately. At such conditions, atmospheres as a whole—not components individually—are subject to phase equilibria with their equilibrium solid phases or liquid phases or both. A molecular-based thermodynamic model for cryogenic chemical systems, referred to as CRYOCHEM, the development of which is still in progress, was shown to reproduce the vertical composition profile of Titan's atmospheric methane measured by the Huygens probe (Tan et al., Icarus 2013, 222, 53). Recently, the model was also used to describe Titan's global circulation where the calculated composition of liquid in Ligeia Mare is consistent with the bathymetry and microwave absorption analysis of T91 Cassini fly-by data (Tan et al., 2014, submitted). Its capability to deal with equilibria involving solid phases has also been demonstrated (Tan et al., Fluid Phase Equilib. 2013, 360, 320). With all those previous works done, our attention is now shifting to the lower temperatures in Titan's tropopause and on Pluto's surface, where much technical development remains for CRYOCHEM to assure adequate performance at low temperatures. In these conditions, solid-vapor equilibrium (SVE) is the dominant phase behavior that determines the composition of the atmosphere and the existing ices. Another potential application is for the subsurface phase equilibrium, which also involves liquid, thus three-phase equilibrium: solid-liquid-vapor (SLV). This presentation will discuss the

  5. Ti1-xAux Alloys: Hard Biocompatible Metals and Their Possible Applications

    NASA Astrophysics Data System (ADS)

    Svanidze, Eteri; Besara, Tiglet; Ozaydin, M. Fevzi; Xin, Yan; Han, Ke; Liang, Hong; Siegrist, Theo; Morosan, Emilia

    2015-03-01

    The search for new hard materials is often challenging from both theoretical and experimental points of view. Furthermore, using materials for biomedical applications calls for alloys with high biocompatibility which are even more sparse. The Ti1-xAux (0 . 22 <= x <= 0 . 8) exhibit extreme hardness and strength values, elevated melting temperatures (compared to those of constituent elements), reduced density compared to Au, high malleability, bulk metallicity, high biocompatibility, low wear, reduced friction, potentially high radio opacity, as well as osseointegration. All these properties render the Ti1-xAux alloys particularly useful for orthopedic, dental, and prosthetic applications, where they could be used as both permanent and temporary components. Additionally, the ability of Ti1-xAux alloys to adhere to ceramic parts could reduce the weight and cost of these components. The work at Rice was supported by NSF DMR 0847681 (E.M. and E.S.).

  6. Development of an unresolved CFD-DEM model for the flow of viscous suspensions and its application to solid-liquid mixing

    NASA Astrophysics Data System (ADS)

    Blais, Bruno; Lassaigne, Manon; Goniva, Christoph; Fradette, Louis; Bertrand, François

    2016-08-01

    Although viscous solid-liquid mixing plays a key role in the industry, the vast majority of the literature on the mixing of suspensions is centered around the turbulent regime of operation. However, the laminar and transitional regimes face considerable challenges. In particular, it is important to know the minimum impeller speed (Njs) that guarantees the suspension of all particles. In addition, local information on the flow patterns is necessary to evaluate the quality of mixing and identify the presence of dead zones. Multiphase computational fluid dynamics (CFD) is a powerful tool that can be used to gain insight into local and macroscopic properties of mixing processes. Among the variety of numerical models available in the literature, which are reviewed in this work, unresolved CFD-DEM, which combines CFD for the fluid phase with the discrete element method (DEM) for the solid particles, is an interesting approach due to its accurate prediction of the granular dynamics and its capability to simulate large amounts of particles. In this work, the unresolved CFD-DEM method is extended to viscous solid-liquid flows. Different solid-liquid momentum coupling strategies, along with their stability criteria, are investigated and their accuracies are compared. Furthermore, it is shown that an additional sub-grid viscosity model is necessary to ensure the correct rheology of the suspensions. The proposed model is used to study solid-liquid mixing in a stirred tank equipped with a pitched blade turbine. It is validated qualitatively by comparing the particle distribution against experimental observations, and quantitatively by compairing the fraction of suspended solids with results obtained via the pressure gauge technique.

  7. Calculation of multicomponent chemical equilibria in gas-solid- liquid systems: calculation methods, thermochemical data, and applications to studies of high-temperature volcanic gases with examples from Mount St. Helens

    USGS Publications Warehouse

    Symonds, R.B.; Reed, M.H.

    1993-01-01

    This paper documents the numerical formulations, thermochemical data base, and possible applications of computer programs, SOLVGAS and GASWORKS, for calculating multicomponent chemical equilibria in gas-solid-liquid systems. SOLVGAS and GASWORKS compute simultaneous equilibria by solving simultaneously a set of mass balance and mass action equations written for all gas species and for all gas-solid or gas-liquid equilibria. Examples of gas-evaporation-from-magma and precipitation-with-cooling calculations for volcanic gases collected from Mount St. Helens are shown. -from Authors

  8. Systems and methods for monitoring a solid-liquid interface

    DOEpatents

    Stoddard, Nathan G; Lewis, Monte A.; Clark, Roger F

    2013-06-11

    Systems and methods are provided for monitoring a solid-liquid interface during a casting process. The systems and methods enable determination of the location of a solid-liquid interface during the casting process.

  9. Photoinduced crystal-to-liquid phase transitions of azobenzene derivatives and their application in photolithography processes through a solid-liquid patterning.

    PubMed

    Norikane, Yasuo; Uchida, Emi; Tanaka, Satoko; Fujiwara, Kyoko; Koyama, Emiko; Azumi, Reiko; Akiyama, Haruhisa; Kihara, Hideyuki; Yoshida, Masaru

    2014-10-01

    The direct and reversible transformation of matter between the solid and liquid phases by light at constant temperature is of great interest because of its potential applications in various manufacturing settings. We report a simple molecular design strategy for the phase transitions: azobenzenes having para-dialkoxy groups with a methyl group at the meta-position. The photolithography processes were demonstrated using the azobenzene as a photoresist in a single process combining development and etching of a copper substrate. PMID:25216186

  10. A sessile drop setup for the time-resolved synchrotron study of solid-liquid interactions: Application to intermetallic formation in 55%Al-Zn alloys

    SciTech Connect

    Bernier, N. De Bruyn, D.; De Craene, M.; Scheers, J.; Claessens, S.; Vaughan, G. B. M.; Vitoux, H.; Gleyzolle, H.; Gorges, B.

    2014-04-28

    We introduce a dedicated setup for measuring by synchrotron diffraction in-situ crystallographic and chemical information at the solid–liquid interface. This setup mostly consists of a double-heating furnace composed of a resistive heating for the solid surface and an inductive heating to produce a liquid droplet. The available high energy and high flux beams allow the rapid reaction kinetics to be investigated with very good time resolution down to 1 ms. An application of this setup is illustrated for the growth mechanisms of intermetallic phases during the hot-dipping of steel in a 55%Al-Zn bath. Results show that the three η-Al{sub 5}Fe{sub 2}, θ-Al{sub 13}Fe{sub 4}, and α-Al{sub 8}Fe{sub 2}Si phases grow at different times and rates during the dipping process, whereas the face-centered cubic AlFe{sub 3} phase is not formed.

  11. Ginzburg-Landau theory for the solid-liquid interface of bcc elements. II - Application to the classical one-component plasma, the Wigner crystal, and He-4

    NASA Technical Reports Server (NTRS)

    Zeng, X. C.; Stroud, D.

    1989-01-01

    The previously developed Ginzburg-Landau theory for calculating the crystal-melt interfacial tension of bcc elements to treat the classical one-component plasma (OCP), the charged fermion system, and the Bose crystal. For the OCP, a direct application of the theory of Shih et al. (1987) yields for the surface tension 0.0012(Z-squared e-squared/a-cubed), where Ze is the ionic charge and a is the radius of the ionic sphere. Bose crystal-melt interface is treated by a quantum extension of the classical density-functional theory, using the Feynman formalism to estimate the relevant correlation functions. The theory is applied to the metastable He-4 solid-superfluid interface at T = 0, with a resulting surface tension of 0.085 erg/sq cm, in reasonable agreement with the value extrapolated from the measured surface tension of the bcc solid in the range 1.46-1.76 K. These results suggest that the density-functional approach is a satisfactory mean-field theory for estimating the equilibrium properties of liquid-solid interfaces, given knowledge of the uniform phases.

  12. Calculation of multicomponent chemical equilibria in gas-solid-liquid systems: Calculation methods, thermochemical data, and applications to studies of high-temperature volcanic gases with examples from Mt. St. Helens

    SciTech Connect

    Symonds, R.B. ); Reed, M.H. )

    1993-10-01

    This paper documents the numerical formulations, thermochemical data base, and possible applications of computer programs, SOLVGAS and GASWORKS, for calculating multicomponent chemical equilibria in gas-solid-liquid systems. SOLVGAS and GASWORKS compute simultaneous equilibria by solving simultaneously a set of mass balance and mass action equations written for all gas species and for all gas-solid or gas-liquid equilibria. The programs interface with a thermo-chemical data base, GASTHERM, which contains coefficients for retrieval of the equilibrium constants from 25[degrees] to 1200[degrees]C. The programs and data base model dynamic chemical processes in 30- to 40-component volcanic-gas systems. The authors can model gas evaporation from magma, mixing of magmatic and hydrothermal gases, precipitation of minerals during pressure and temperature decrease, mixing of volcanic gas with air, and reaction of gases with wall rock. Examples are given of the gas-evaporation-from-magma and precipitation-with-cooling calculations for volcanic gases collected from Mt. St. Helens in September 1981. The authors predict: (1) the amounts of trace elements volatilized from shallow magma, deep magma, and wall rock, and (2) the solids that precipitate from the gas upon cooling. The predictions are tested by comparing them with the measured trace-element concentrations in gases and the observed sublimate sequence. This leads to the following conclusions: (1) most of the trace elements in the Mt. St. Helens gases are volatilized from shallow magma as simple chlorides; (2) some elements (for example, Al, Ca) exist dominantly in rock aerosols, not gases, in the gas stream; (3) near-surface cooling of the gases triggers precipitation of oxides, sulfides, halides, tungstates, and native elements; and (4) equilibrium cooling of the gases to 100[degrees]C causes most trace elements, except for Hg, Sb, and Se, to precipitate from the gas. 94 refs., 30 figs., 7 tabs.

  13. Ultrasonic characterization of solid liquid suspensions

    DOEpatents

    Panetta, Paul D.

    2010-06-22

    Using an ultrasonic field, properties of a solid liquid suspension such as through-transmission attenuation, backscattering, and diffuse field are measured. These properties are converted to quantities indicating the strength of different loss mechanisms (such as absorption, single scattering and multiple scattering) among particles in the suspension. Such separation of the loss mechanisms can allow for direct comparison of the attenuating effects of the mechanisms. These comparisons can also indicate a model most likely to accurately characterize the suspension and can aid in determination of properties such as particle size, concentration, and density of the suspension.

  14. Solid-liquid phase transition in argon

    NASA Technical Reports Server (NTRS)

    Tsang, T.; Tang, H. T.

    1978-01-01

    Starting from the Lennard-Jones interatomic potential, a modified cell theory has been used to describe the solid-liquid phase transition in argon. The cell-size variations may be evaluated by a self-consistent condition. With the inclusion of cell-size variations, the transition temperature, the solid and liquid densities, and the liquid-phase radial-distribution functions have been calculated. These ab initio results are in satisfactory agreement with molecular-dynamics calculations as well as experimental data on argon.

  15. Precise AuxPt1-x Alloy Nanoparticle Array of Tunable Composition for Catalytic Applications

    NASA Astrophysics Data System (ADS)

    Jahn, Sarah; Lechner, Sebastian J.; Freichels, Helene; Möller, Martin; Spatz, Joachim P.

    2016-02-01

    A 3-dimensional Block Copolymer Micellar nanoLithography (BCML) process was used to prepare AuxPt1-x alloy nanoparticles (NPs) monodisperse in size and composition, strongly anchored onto SiO2-particles (0.2 wt.% AuxPt1-x/SiO2). The particles possess a face-centered cubic (fcc) crystal structure and their size could be varied from 3-12 nm. We demonstrate the uniformity of the Au/Pt composition by analyzing individual NPs by energy-dispersive X-ray spectroscopy. The strongly bound AuxPt1-x NPs catalyzed the oxidation of CO with high activity. Thermal ageing experiments in pure CO2 as well as in ambient atmosphere demonstrated stability of the size distribution for times as long as 22 h.

  16. Redistribution of fluorescent molecules at the solid/liquid interface with total internal reflection illumination.

    PubMed

    Wei, Lin; Ye, Zhongju; Luo, Wenjuan; Chen, Bo; Xiao, Lehui

    2016-08-01

    Many intriguing physical and chemical processes commonly take place at the solid/liquid interface. Total internal reflection illumination, together with single molecule spectroscopy, provides a robust platform for the selective exploration of kinetic processes close the interface. With these techniques, it was observed that the distribution of Rhodamine B molecules close to a solid/liquid interface could be regulated in a photo-induced route. The laser-induced repulsion force at this interface is enough to compromise the Brownian diffusion of single molecules in a range of several hundred nanometers normal to the solid/liquid interface. This observation is fundamentally and practically interesting because moderate laser intensity is enough to initiate this repulsion effect. Therefore, it might display extensive applications in the development of photo-modulation technique with high throughput capability. PMID:27216678

  17. Coarsening in binary solid-liquid mixtures

    NASA Technical Reports Server (NTRS)

    Voorhees, P. W.

    1990-01-01

    A theory of Ostwald ripening has been developed for a solid-liquid mixture cosisting of a low volume fraction array of spherical solid particles in a liquid wherein the coarsening process proceeds via the transport of both heat and mass. It is found that the simultaneous transport of heat and mass during ripening does not alter the exponents of the temporal power laws governing the ripening process from their classical values but does alter the amplitudes of these power laws. The growth rate of the cube of the average particle radius, the rate constant, is found to depend both on the alloy solute concentration and the ratio of the thermal to solutal diffusivities. In most metallic systems, a large decrease in the rate constant can be expected with small additions of solute to a pure metal. Possible extensions of this theory to the analogous problem of ripening in isothermal ternary alloys are also discussed.

  18. An immersed boundary-thermal lattice Boltzmann method for solid-liquid phase change

    NASA Astrophysics Data System (ADS)

    Huang, Rongzong; Wu, Huiying

    2014-11-01

    In this work, an immersed boundary-thermal lattice Boltzmann method (IB-TLBM) is proposed to simulate solid-liquid phase change problems. To treat the velocity and temperature boundary conditions on the solid-liquid interface, immersed boundary method (IBM) is adopted, in which the solid-liquid interface is represented as a sharp interface rather than a diffusive interface and is tracked explicitly by Lagrangian grid. The surface forces along the immersed boundary, including the “momentum force” for velocity boundary condition and the “energy force” for temperature boundary condition, are calculated by the direct-forcing scheme. The moving velocity of solid-liquid interface induced by phase change is calculated by the amount of latent heat absorbed or released in a time step directly, with no need to compute temperature gradients in solid and liquid phases separately. The temperature on the solid-liquid interface is specified as the melting temperature, which means phase change happens at a constant temperature. As the solid-liquid interface evolves with time, the identification of phase of Eulerian points and the rearrangement of Lagrangian points are also considered. With regard to the velocity and temperature fields, passive scalar thermal lattice Boltzmann method (TLBM) with multiple-relaxation-time (MRT) collision schemes is adopted. Numerical examples, including conduction-induced melting in a semi-infinite space and melting in a square cavity, are carried out to verify the present method and good results are obtained. As a further application, melting in a circular cylinder with considering the motion of solid phase is simulated successfully by the present method; numerical results show that the motion of solid phase accelerates the melting process obviously.

  19. Computational Investigations of Solid-Liquid Interfaces

    SciTech Connect

    Mark Asta

    2011-08-31

    In a variety of materials synthesis and processing contexts, atomistic processes at heterophase interfaces play a critical role governing defect formation, growth morphologies, and microstructure evolution. Accurate knowledge of interfacial structure, free energies, mobilities and segregation coefficients are critical for predictive modeling of microstructure evolution, yet direct experimental measurement of these fundamental interfacial properties remains elusive in many cases. In this project first-principles calculations were combined with molecular-dynamics (MD) and Monte-Carlo (MC) simulations, to investigate the atomic-scale structural and dynamical properties of heterophase interfaces, and the relationship between these properties and the calculated thermodynamic and kinetic parameters that influence the evolution of phase transformation structures at nanometer to micron length scales. The topics investigated in this project were motivated primarily by phenomena associated with solidification processing of metals and alloys, and the main focus of the work was thus on solid-liquid interfaces and high-temperature grain boundaries. Additional efforts involved first-principles calculations of coherent solid-solid heterophase interfaces, where a close collaboration with researchers at the National Center for Electron Microscopy was undertaken to understand the evolution of novel core-shell precipitate microstructures in aluminum alloys.

  20. An improved technique for modeling initial reservoir hydrocarbon saturation distributions: Applications in Illinois (USA) aux vases oil reservoirs

    USGS Publications Warehouse

    Udegbunam, E.; Amaefule, J.O.

    1998-01-01

    An improved technique for modeling the initial reservoir hydrocarbon saturation distributions is presented. In contrast to the Leverett J-function approach, this methodology (hereby termed flow-unit-derived initial oil saturation or FUSOI) determines the distributions of the initial oil saturations from a measure of the mean hydraulic radius, referred to as the flow zone indicator (FZI). FZI is derived from porosity and permeability data. In the FUSOI approach, capillary pressure parameters, S(wir), P(d), and ??, derived from the Brooks and Corey (1966) model [Brooks, R.H., Corey, A.T., 1966. Hydraulic properties of porous media, Hydrology Papers, Colorado State Univ., Ft. Collins, No. 3, March.], are correlated to the FZI. Subsequent applications of these parameters then permit the computation of improved hydrocarbon saturations as functions of FZI and height above the free water level (FWL). This technique has been successfully applied in the Mississippian Aux Vases Sandstone reservoirs of the Illinois Basin (USA). The Aux Vases Zeigler field (Franklin County, IL, USA) was selected for a field-wide validation of this FUSOI approach because of the availability of published studies. With the initial oil saturations determined on a depth-by-depth basis in cored wells, it was possible to geostatistically determine the three-dimensional (3-D) distributions of initial oil saturations in the Zeigler field. The original oil-in-place (OOIP), computed from the detailed initialization of the 3-D reservoir simulation model of the Zeigler field, was found to be within 5.6% of the result from a rigorous material balance method.An improved technique for modeling the initial reservoir hydrocarbon saturation distributions is presented. In contrast to the Leverett J-function approach, this methodology (hereby termed flow-unit-derived initial oil saturation or FUSOI) determines the distributions of the initial oil saturations from a measure of the mean hydraulic radius, referred to

  1. Quantitative modeling of the equilibration of two-phase solid-liquid Fe by atomistic simulations on diffusive time scales

    NASA Astrophysics Data System (ADS)

    Asadi, Ebrahim; Asle Zaeem, Mohsen; Nouranian, Sasan; Baskes, Michael I.

    2015-01-01

    In this paper, molecular dynamics (MD) simulations based on the modified-embedded atom method (MEAM) and a phase-field crystal (PFC) model are utilized to quantitatively investigate the solid-liquid properties of Fe. A set of second nearest-neighbor MEAM parameters for high-temperature applications are developed for Fe, and the solid-liquid coexisting approach is utilized in MD simulations to accurately calculate the melting point, expansion in melting, latent heat, and solid-liquid interface free energy, and surface anisotropy. The required input properties to determine the PFC model parameters, such as liquid structure factor and fluctuations of atoms in the solid, are also calculated from MD simulations. The PFC parameters are calculated utilizing an iterative procedure from the inputs of MD simulations. The solid-liquid interface free energy and surface anisotropy are calculated using the PFC simulations. Very good agreement is observed between the results of our calculations from MEAM-MD and PFC simulations and the available modeling and experimental results in the literature. As an application of the developed model, the grain boundary free energy of Fe is calculated using the PFC model and the results are compared against experiments.

  2. Solid-liquid critical behavior of water in nanopores.

    PubMed

    Mochizuki, Kenji; Koga, Kenichiro

    2015-07-01

    Nanoconfined liquid water can transform into low-dimensional ices whose crystalline structures are dissimilar to any bulk ices and whose melting point may significantly rise with reducing the pore size, as revealed by computer simulation and confirmed by experiment. One of the intriguing, and as yet unresolved, questions concerns the observation that the liquid water may transform into a low-dimensional ice either via a first-order phase change or without any discontinuity in thermodynamic and dynamic properties, which suggests the existence of solid-liquid critical points in this class of nanoconfined systems. Here we explore the phase behavior of a model of water in carbon nanotubes in the temperature-pressure-diameter space by molecular dynamics simulation and provide unambiguous evidence to support solid-liquid critical phenomena of nanoconfined water. Solid-liquid first-order phase boundaries are determined by tracing spontaneous phase separation at various temperatures. All of the boundaries eventually cease to exist at the critical points and there appear loci of response function maxima, or the Widom lines, extending to the supercritical region. The finite-size scaling analysis of the density distribution supports the presence of both first-order and continuous phase changes between solid and liquid. At around the Widom line, there are microscopic domains of two phases, and continuous solid-liquid phase changes occur in such a way that the domains of one phase grow and those of the other evanesce as the thermodynamic state departs from the Widom line. PMID:26100904

  3. Precise AuxPt1−x Alloy Nanoparticle Array of Tunable Composition for Catalytic Applications

    PubMed Central

    Jahn, Sarah; Lechner, Sebastian J.; Freichels, Helene; Möller, Martin; Spatz, Joachim P.

    2016-01-01

    A 3-dimensional Block Copolymer Micellar nanoLithography (BCML) process was used to prepare AuxPt1−x alloy nanoparticles (NPs) monodisperse in size and composition, strongly anchored onto SiO2-particles (0.2 wt.% AuxPt1−x/SiO2). The particles possess a face-centered cubic (fcc) crystal structure and their size could be varied from 3–12 nm. We demonstrate the uniformity of the Au/Pt composition by analyzing individual NPs by energy-dispersive X-ray spectroscopy. The strongly bound AuxPt1−x NPs catalyzed the oxidation of CO with high activity. Thermal ageing experiments in pure CO2 as well as in ambient atmosphere demonstrated stability of the size distribution for times as long as 22 h. PMID:26856888

  4. Self-instability of finite sized solid-liquid interfaces

    PubMed Central

    Wu, L.K.; Xu, B.; Li, Q.L.; Liu, W.

    2015-01-01

    In solid-liquid systems, macroscopic solids lose their equilibrium and melt in a manner that results in overall movement of the solid-liquid interface. This phenomenon occurs when they are subjected to temperature gradients or external stress, for example. However, many experiments suggest that the melting of nano- and micro-sized metallic nuclei follows a different process not described by traditional melting theory. In this paper, we demonstrate through simulation that the melting of solid nuclei of these sizes occurs via random breaches at the interfaces. Moreover, this breaching process occurs at the exact solid-liquid equilibrium temperature and in the absence of any external disturbance, which suggests the name “self-instability” for this melting process. We attribute this spontaneous instability to the curvature of the samples; based on the relationship between the sample’s instability and its curvature, we propose a destabilizing model for small systems. This model fits well with experimental results and leads to new insights into the instability behavior of small-sized systems; these insights have broad implications for research topics ranging from dendrite self-fragmentation to nanoparticle instability. PMID:26685800

  5. Methods and systems for monitoring a solid-liquid interface

    SciTech Connect

    Stoddard, Nathan G.; Clark, Roger F.; Kary, Tim

    2010-07-20

    Methods and systems are provided for monitoring a solid-liquid interface, including providing a vessel configured to contain an at least partially melted material; detecting radiation reflected from a surface of a liquid portion of the at least partially melted material that is parallel with the liquid surface; measuring a disturbance on the surface; calculating at least one frequency associated with the disturbance; and determining a thickness of the liquid portion based on the at least one frequency, wherein the thickness is calculated based on.times. ##EQU00001## where g is the gravitational constant, w is the horizontal width of the liquid, and f is the at least one frequency.

  6. Modelling temperature and concentration dependent solid/liquid interfacial energies

    NASA Astrophysics Data System (ADS)

    Lippmann, Stephanie; Jung, In-Ho; Paliwal, Manas; Rettenmayr, Markus

    2016-01-01

    Models for the prediction of the solid/liquid interfacial energy in pure substances and binary alloys, respectively, are reviewed and extended regarding the temperature and concentration dependence of the required thermodynamic entities. A CALPHAD-type thermodynamic database is used to introduce temperature and concentration dependent melting enthalpies and entropies for multicomponent alloys in the temperature range between liquidus and solidus. Several suitable models are extended and employed to calculate the temperature and concentration dependent interfacial energy for Al-FCC with their respective liquids and compared with experimental data.

  7. A hybrid solid-liquid polymer photodiode for the bioenvironment

    NASA Astrophysics Data System (ADS)

    Antognazza, M. R.; Ghezzi, D.; Musitelli, D.; Garbugli, M.; Lanzani, G.

    2009-06-01

    We demonstrate that a prototypical semiconducting polymer, poly[2-methoxy-5-(2'-ethylhexyloxy)-p-phenylene vinylene] (MEH-PPV) maintains unaltered its optoelectronic properties throughout the various steps for neural preparation. Films of MEH-PPV, after prolonged immersion in water or buffer solution, are characterized by linear and nonlinear optical spectroscopy. Based on this result, we introduce a hybrid solid-liquid photodiode based on MEH-PPV, in which we use culturing media as liquid, ionic cathodes. The hybrid device is proposed as an active interface between living tissue and conducting polymers for cell diagnostic and neural implants.

  8. UV patterned nanoporous solid-liquid core waveguides.

    PubMed

    Gopalakrishnan, Nimi; Sagar, Kaushal S; Christiansen, Mads Brøkner; Vigild, Martin E; Ndoni, Sokol; Kristensen, Anders

    2010-06-01

    Nanoporous Solid-Liquid core waveguides were prepared by UV induced surface modification of hydrophobic nanoporous polymers. With this method, the index contrast (deltan = 0.20) is a result of selective water infiltration. The waveguide core is defined by UV light, rendering the exposed part of a nanoporous polymer block hydrophilic. A propagation loss of 0.62 dB/mm and a bend loss of 0.81 dB/90 degrees for bend radius as low as 1.75 mm was obtained in these multimode waveguides. PMID:20588419

  9. Bioinspired solid-liquid mixed tunable lens with multilayered structure

    NASA Astrophysics Data System (ADS)

    Liang, Dan; Wang, Xuan-Yin; Du, Jia-Wei

    2015-06-01

    A solid-liquid mixed tunable lens with multilayered structure is proposed. The designed lens utilizes a solid-state elastic polymer, optical liquid, and glass as the optical medium, and adjusts the focus by changing the surface curvature of the elastic polymer. The integrated structure of the tunable lens is presented, as well as detailed descriptions of the lens materials, fabrication, and assembling process. Images captured through the tunable lens under different displacement loads are presented, and the relationship among the displacement load, curvature radius, and effective focal length is analyzed. Additionally, the optical property of the tunable lens is simulated using the ZEMAX software. A change in focal length from 14.8 mm to 30 mm is demonstrated within the tiny 0.12 mm variation of the displacement load. Numerical analyses show that the lens distortion is less than 2%, and the modulation transfer function reaches 67 line pairs per mm. The solid-liquid mixed tunable lens shows the potential for developing a compact, low-aberration, and stable optical system.

  10. Solid-liquid work of adhesion of coarse-grained models of n-hexane on graphene layers derived from the conditional reversible work method

    SciTech Connect

    Ardham, Vikram Reddy; Leroy, Frédéric E-mail: f.leroy@theo.chemie.tu-darmstadt.de; Deichmann, Gregor; Vegt, Nico F. A. van der E-mail: f.leroy@theo.chemie.tu-darmstadt.de

    2015-12-28

    We address the question of how reducing the number of degrees of freedom modifies the interfacial thermodynamic properties of heterogeneous solid-liquid systems. We consider the example of n-hexane interacting with multi-layer graphene which we model both with fully atomistic and coarse-grained (CG) models. The CG models are obtained by means of the conditional reversible work (CRW) method. The interfacial thermodynamics of these models is characterized by the solid-liquid work of adhesion W{sub SL} calculated by means of the dry-surface methodology through molecular dynamics simulations. We find that the CRW potentials lead to values of W{sub SL} that are larger than the atomistic ones. Clear understanding of the relationship between the structure of n-hexane in the vicinity of the surface and W{sub SL} is elucidated through a detailed study of the energy and entropy components of W{sub SL}. We highlight the crucial role played by the solid-liquid energy fluctuations. Our approach suggests that CG potentials should be designed in such a way that they preserve the range of solid-liquid interaction energies, but also their fluctuations in order to preserve the reference atomistic value of W{sub SL}. Our study thus opens perspectives into deriving CG interaction potentials that preserve the thermodynamics of solid-liquid contacts and will find application in studies that intend to address materials driven by interfaces.

  11. Resolving amorphous solid-liquid interfaces by atomic force microscopy

    NASA Astrophysics Data System (ADS)

    Burson, Kristen M.; Gura, Leonard; Kell, Burkhard; Büchner, Christin; Lewandowski, Adrian L.; Heyde, Markus; Freund, Hans-Joachim

    2016-05-01

    Recent advancements in liquid atomic force microscopy make it an ideal technique for probing the structure of solid-liquid interfaces. Here, we present a structural study of a two-dimensional amorphous silica bilayer immersed in an aqueous solution utilizing liquid atomic force microscopy with sub-nanometer resolution. Structures show good agreement with atomically resolved ultra-high vacuum scanning tunneling microscopy images obtained on the same sample system, owing to the structural stability of the silica bilayer and the imaging clarity from the two-dimensional sample system. Pair distance histograms of ring center positions are utilized to develop quantitative metrics for structural comparison, and the physical origin of pair distance histogram peaks is addressed by direct assessment of real space structures.

  12. Solid/liquid interfacial free energies in binary systems

    NASA Technical Reports Server (NTRS)

    Nason, D.; Tiller, W. A.

    1973-01-01

    Description of a semiquantitative technique for predicting the segregation characteristics of smooth interfaces between binary solid and liquid solutions in terms of readily available thermodynamic parameters of the bulk solutions. A lattice-liquid interfacial model and a pair-bonded regular solution model are employed in the treatment with an accommodation for liquid interfacial entropy. The method is used to calculate the interfacial segregation and the free energy of segregation for solid-liquid interfaces between binary solutions for the (111) boundary of fcc crystals. The zone of compositional transition across the interface is shown to be on the order of a few atomic layers in width, being moderately narrower for ideal solutions. The free energy of the segregated interface depends primarily upon the solid composition and the heats of fusion of the component atoms, the composition difference of the solutions, and the difference of the heats of mixing of the solutions.

  13. Methods and systems for monitoring a solid-liquid interface

    SciTech Connect

    Stoddard, Nathan G.; Clark, Roger F.

    2011-10-04

    Methods and systems are provided for monitoring a solid-liquid interface, including providing a vessel configured to contain an at least partially melted material; detecting radiation reflected from a surface of a liquid portion of the at least partially melted material; providing sound energy to the surface; measuring a disturbance on the surface; calculating at least one frequency associated with the disturbance; and determining a thickness of the liquid portion based on the at least one frequency, wherein the thickness is calculated based on L=(2m-1)v.sub.s/4f, where f is the frequency where the disturbance has an amplitude maximum, v.sub.s is the speed of sound in the material, and m is a positive integer (1, 2, 3, . . . ).

  14. Solid-liquid coexistence of polydisperse fluids via simulation.

    PubMed

    Wilding, Nigel B

    2009-03-14

    We describe a simulation method for the accurate study of the equilibrium freezing properties of polydisperse fluids under the experimentally relevant condition of fixed polydispersity. The approach is based on the phase switch Monte Carlo method of Wilding and Bruce [Phys. Rev. Lett. 85, 5138 (2000)]. This we have generalized to deal with particle size polydispersity by incorporating updates which alter the diameter sigma of a particle, under the control of a distribution of chemical potential differences mu(sigma). Within the resulting isobaric semi-grand-canonical ensemble, we detail how to adapt mu(sigma) and the applied pressure such as to study coexistence, while ensuring that the ensemble averaged density distribution rho(sigma) matches a fixed functional form. Results are presented for the effects of small degrees of polydispersity on the solid-liquid transition of soft spheres. PMID:19292519

  15. Transport phenomena during solid-liquid phase change in porous media

    SciTech Connect

    Pak, J.; Plumb, O.A.

    1995-12-31

    Transport phenomena in porous media with phase change has been studied in a wide variety of both environmental and engineering systems during the past several decades. Examples of applications of interest include the freezing and melting of soils, thermal energy storage, and post accident analysis of nuclear reactors. The present study focuses on the solid-liquid phase change occurring during the melting of a packed bed. Particular attention is paid to the redistribution of mass. The results are applicable to the manufacture of powder based composites, ceramic-metal or certain metal-metal combinations. Due to the process used in producing ceramics and advanced alloys, many of the raw materials utilized in advanced composites are powders. The objective of the present study is to develop a general model for solid-liquid phase change which results from the application of heat to a porous structure. The system of interest is a packed bed which contains melting and non melting components. A one-dimensional phase change process is examined in this study. The macroscopic energy equation and continuity equations for both the liquid and solid phases are solved numerically and experiments are conducted to confirm the numerical results. The non melting particles used in the experiments are spherical glass beads. Salol (benzoic acid 2-hydroxyphenylester) is chosen as the phase change material because of its low melting temperature and available thermophysical properties. During the melting process, redistribution of the mass of salol was monitored utilizing gamma attenuation and compared with the numerical results. The effects of varying the particle diameter and the geometric melting model from constant volume to constant porosity are discussed.

  16. Mechanisms of reduced solute diffusivity at nanoconfined solid-liquid interface

    NASA Astrophysics Data System (ADS)

    Mahadevan, T.; Kojic, M.; Ferrari, M.; Ziemys, A.

    2013-06-01

    We report results from molecular simulations that reveal the causes of reduced diffusivity at solid-liquid interfaces in the presence of nanoscale confinement. The diffusion of a 2 M glucose solution was simulated inside a 10 nm silica channel together with the calculated thermodynamic properties of diffusion. A strong energy-entropy compensation mechanism was found at the interface with a free energy minimum of -0.6 kcal/mol. Using the Eyring equation the average jump length was reduced by 15% at interface. The complete loss of solute diffusivity at silica surface was explained by the substantial loss of the probability of productive displacements. The results suggested that glucose molecule diffusivity close to the surface might be related to a stiffer cage of the hydration shell, which affects the probability of cage breaking. These results help in understanding of diffusion mechanisms at interface and predicting mass transport in nanoconfinement for engineering and biomedical applications.

  17. Intermetallic Compound Formation Mechanisms for Cu-Sn Solid-Liquid Interdiffusion Bonding

    NASA Astrophysics Data System (ADS)

    Liu, H.; Wang, K.; Aasmundtveit, K. E.; Hoivik, N.

    2012-09-01

    Cu-Sn solid-liquid interdiffusion (SLID) bonding is an evolving technique for wafer-level packaging which features robust, fine pitch and high temperature tolerance. The mechanisms of Cu-Sn SLID bonding for wafer-level bonding and three-dimensional (3-D) packaging applications have been studied by analyzing the microstructure evolution of Cu-Sn intermetallic compounds (IMCs) at elevated temperature up to 400°C. The bonding time required to achieve a single IMC phase (Cu3Sn) in the final interconnects was estimated according to the parabolic growth law with consideration of defect-induced deviation. The effect of predominantly Cu metal grain size on the Cu-Sn interdiffusion rate is discussed. The temperature versus time profile (ramp rate) is critical to control the morphology of scallops in the IMC. A low temperature ramp rate before reaching the bonding temperature is believed to be favorable in a SLID wafer-level bonding process.

  18. Interaction of Porosity with a Planar Solid/Liquid Interface

    NASA Technical Reports Server (NTRS)

    Catalina, Adrian V.; Stefanescu, Doru M.; Sen, Subhayu; Kaukler, William F.

    2004-01-01

    In this article, an investigation of the interaction between gas porosity and a planar solid/liquid (SL) interface is reported. A two-dimensional numerical model able to accurately track sharp SL interfaces during solidification of pure metals and alloys is proposed. The finite-difference method and a rectangular undeformed grid are used for computation. The SL interface is described through the points of intersection with the grid lines. Its motion is determined by the thermal and solute gradients at each particular point. Changes of the interface temperature because of capillarity or solute redistribution as well as any perturbation of the thermal and solute field produced by the presence of non-metallic inclusions can be computed. To validate the model, the dynamics of the interaction between a gas pore and a solidification front in metal alloys was observed using a state of the art X-ray transmission microscope (XTM). The experiments included observation of the distortion of the SL interface near a pore, real-time measurements of the growth rate, and the change in shape of the porosity during interaction with the SL interface in pure Al and Al-0.25 wt pct Au alloy. In addition, porosity-induced solute segregation patterns surrounding a pore were also quantified.

  19. Solid-Liquid Self-Adaptive Polymeric Composite.

    PubMed

    Dong, Pei; Chipara, Alin Cristian; Loya, Phillip; Yang, Yingchao; Ge, Liehui; Lei, Sidong; Li, Bo; Brunetto, Gustavo; Machado, Leonardo D; Hong, Liang; Wang, Qizhong; Yang, Bilan; Guo, Hua; Ringe, Emilie; Galvao, Douglas S; Vajtai, Robert; Chipara, Mircea; Tang, Ming; Lou, Jun; Ajayan, Pulickel M

    2016-01-27

    A solid-liquid self-adaptive composite (SAC) is synthesized using a simple mixing-evaporation protocol, with poly(dimethylsiloxane) (PDMS) and poly(vinylidene fluoride) (PVDF) as active constituents. SAC exists as a porous solid containing a near equivalent distribution of the solid (PVDF)-liquid (PDMS) phases, with the liquid encapsulated and stabilized within a continuous solid network percolating throughout the structure. The pores, liquid, and solid phases form a complex hierarchical structure, which offers both mechanical robustness and a significant structural adaptability under external forces. SAC exhibits attractive self-healing properties during tension, and demonstrates reversible self-stiffening properties under compression with a maximum of 7-fold increase seen in the storage modulus. In a comparison to existing self-healing and self-stiffening materials, SAC offers distinct advantages in the ease of fabrication, high achievable storage modulus, and reversibility. Such materials could provide a new class of adaptive materials system with multifunctionality, tunability, and scale-up potentials. PMID:26720058

  20. Solid-Liquid Interface Characterization Hardware: Advanced Technology Development (ATD)

    NASA Technical Reports Server (NTRS)

    Peters, Palmer N.; Sisk, R. C.; Sen, S.; Kaukler, W. F.; Curreri, Peter A.; Wang, F. C.; Rose, M. Franklin (Technical Monitor)

    2000-01-01

    This ATD has the goal of enabling the integration of three separate measurement techniques to characterize the solid-liquid interface of directionally solidified materials in real-time. Arrays of film-based metal thermocouple elements are under development along with compact Seebeck furnaces suitable for interfacing with separately developed X-ray Transmission Microscopes. Results of applying film arrays to furnace profiling are shown, demonstrating their ability to identify a previously undetected hardware flaw in the development of a second-generation compact furnace. Results of real-time furnace profiling also confirmed that the compact furnace design effectively isolates the temperature profiles in two halves of the furnace, a necessary feature. This isolation had only been inferred previously from the characteristics of Seebeck data reported. Results from a 24-thermocouple array successfully monitoring heating and isothermal cooling of a tin sample are shown. The importance of non-intrusion by the arrays, as well as furnace design, on the profiling of temperature gradients is illustrated with example measurements. Further developments underway for effectively combining all three measurements are assessed in terms of improved x-ray transmission, increased magnification, integral arrays with minimum intrusion, integral scales for velocity measurements and other features being incorporated into the third generation Seebeck furnace under construction.

  1. Solid-liquid phase boundaries of lens protein solutions.

    PubMed Central

    Berland, C R; Thurston, G M; Kondo, M; Broide, M L; Pande, J; Ogun, O; Benedek, G B

    1992-01-01

    We report measurement of the solid-liquid phase boundary, or liquidus line, for aqueous solutions of three pure calf gamma-crystallin proteins: gamma II, gamma IIIa, and gamma IIIb. We also studied the liquidus line for solutions of native gamma IV-crystallin calf lens protein, which consists of 85% gamma IVa/15% gamma IVb. In all four proteins the liquidus phase boundaries lie higher in temperature than the previously determined liquid-liquid coexistence curves. Thus, over the range of concentration and temperature for which liquid-liquid phase separation occurs, the coexistence of a protein crystal phase with a protein liquid solution phase is thermodynamically stable relative to the metastable separated liquid phases. The location of the liquidus lines clearly divides these four crystallin proteins into two groups: those in which liquidus lines flatten at temperatures greater than 70 degrees C: gamma IIIa and gamma IV, and those in which liquidus lines flatten at temperatures less than 50 degrees C: gamma II and gamma IIIb. We have analyzed the form of the liquidus lines by using specific choices for the structures of the Gibbs free energy in solution and solid phases. By applying the thermodynamic conditions for equilibrium between the two phases to the resulting chemical potentials, we can estimate the temperature-dependent free energy change upon binding of protein and water into the solid phase. PMID:1741375

  2. Final Report: Thermal Conductance of Solid-Liquid Interfaces

    SciTech Connect

    Cahil, David, G.; Braun, Paul, V.

    2006-05-31

    Research supported by this grant has significantly advanced fundamental understanding of the thermal conductance of solid-liquid interfaces, and the thermal conductivity of nanofluids and nanoscale composite materials. • The thermal conductance of interfaces between carbon nanotubes and a surrounding matrix of organic molecules is exceptionally small and this small value of the interface conductance limits the enhancement in thermal conductivity that can be achieved by loading a fluid or a polymer with nanotubes. • The thermal conductance of interfaces between metal nanoparticles coated with hydrophilic surfactants and water is relatively high and surprisingly independent of the details of the chemical structure of the surfactant. • We extended our experimental methods to enable studies of planar interfaces between surfactant-coated metals and water where the chemical functionalization can be varied between strongly hydrophobic and strongly hydrophilic. The thermal conductance of hydrophobic interfaces establishes an upper-limit of 0.25 nm on the thickness of the vapor-layer that is often proposed to exist at hydrophobic interfaces. • Our high-precision measurements of fluid suspensions show that the thermal conductivity of fluids is not significantly enhanced by loading with a small volume fraction of spherical nanoparticles. These experimental results directly contradict some of the anomalous results in the recent literature and also rule-out proposed mechanisms for the enhanced thermal conductivity of nanofluids that are based on modification of the fluid thermal conductivity by the coupling of fluid motion and the Brownian motion of the nanoparticles.

  3. Probing Hydrophilic Interface of Solid/Liquid-Water by Nanoultrasonics

    PubMed Central

    Mante, Pierre-Adrien; Chen, Chien-Cheng; Wen, Yu-Chieh; Chen, Hui-Yuan; Yang, Szu-Chi; Huang, Yu-Ru; -Ju Chen, I.; Chen, Yun-Wen; Gusev, Vitalyi; Chen, Miin-Jang; Kuo, Jer-Lai; Sheu, Jinn-Kong; Sun, Chi-Kuang

    2014-01-01

    Despite the numerous devoted studies, water at solid interfaces remains puzzling. An ongoing debate concerns the nature of interfacial water at a hydrophilic surface, whether it is more solid-like, ice-like, or liquid-like. To answer this question, a complete picture of the distribution of the water molecule structure and molecular interactions has to be obtained in a non-invasive way and on an ultrafast time scale. We developed a new experimental technique that extends the classical acoustic technique to the molecular level. Using nanoacoustic waves with a femtosecond pulsewidth and an ångström resolution to noninvasively diagnose the hydration structure distribution at ambient solid/water interface, we performed a complete mapping of the viscoelastic properties and of the density in the whole interfacial water region at hydrophilic surfaces. Our results suggest that water in the interfacial region possesses mixed properties and that the different pictures obtained up to now can be unified. Moreover, we discuss the effect of the interfacial water structure on the abnormal thermal transport properties of solid/liquid interfaces. PMID:25176017

  4. Interaction of Porosity with a Planar Solid/Liquid Interface

    NASA Technical Reports Server (NTRS)

    Catalina, Adrian V.; Stefanescu, Doru M.; Sen, Subhayu; Kaukler, William K.; Curreri, Peter A. (Technical Monitor)

    2002-01-01

    In this paper, an investigation of the interaction between gas porosity and a planar solid/liquid (SL) interface is reported. A two-dimensional numerical model able to accurately track sharp SL interfaces during solidification of pure metals and alloys is proposed. The finite difference method and a rectangular undeformed grid are used for computation. The SL interface is described through the points of intersection with the grid lines. Its motion is determined by the thermal and solute gradients at each particular point. Changes of the interface temperature because of capillarity or solute redistribution as well as any perturbation of the thermal and solute field produced by the presence of non-metallic inclusions can be computed. To validate the model, the dynamics of the interaction between a gas pore and a solidification front in metal alloys was observed using a state of the art X-ray Transmission Microscope. The experiments included observation of the distortion of the SL interface near a pore, real-time measurements of the growth rate and the change in shape of the porosity during interaction with an advancing SL interface in pure Al and Al-0.25 wt% Au alloy. In addition, porosity induced solute segregation patterns surrounding a pore were also quantified.

  5. Wastewater Triad Project: Solid-Liquid Separator FY 2000 Deployment

    SciTech Connect

    Walker, J.F.

    2001-01-11

    The Wastewater Triad Project (WTP) consists of three operational units: the cesium removal (CsR) system, the out-of-tank evaporator (OTE) system, and the solid/liquid separation (SLS) system. These systems were designed to reduce the volume and radioactivity of low-level liquid waste (LLLW) stored in the Melton Valley Storage Tanks (MVSTs) and are operated independently or in series in order to accomplish the treatment goals. Each is a modular, skid-mounted system that is self-contained, individually shielded, and designed to be decontaminated and removed once the project has been completed. The CsR and OTE systems are installed inside Building 7877; the SLS system is installed adjacent to the east side of the MVST 7830 vault cover. The CsR, which consists of ion-exchange equipment for removing {sup 137}Cs from LLLW, was demonstrated in 1997. During the Cesium Removal Demonstration, 30,853 gal of radioactive supernate was processed and 1142 Ci of {sup 137}Cs was removed from the supernate and loaded onto 70 gal of a crystalline silicotitanate sorbent manufactured by UOP, Inc. The OTE system is a subatmospheric single-stage evaporator system designed to concentrate LLLW to smaller volumes. It was previously demonstrated in 1996 and was operated in 1998 to process about 80,000 gal of LLLW. The SLS system was designed to filter and remove suspended solids from LLLW in order to minimize further accumulation of sludge in new storage tanks or to prevent fouling of CsR and OTE systems. The SLS was installed and demonstrated in 1999; {approximately}45,000 gal of radioactive supernate was processed during the demonstration.

  6. Coarsening in Solid Liquid Systems: A Verification of Fundamental Theory

    NASA Astrophysics Data System (ADS)

    Thompson, John D.

    Coarsening is a process that occurs in nearly all multi-phase materials in which the total energy of a system is reduced through the reduction of total interfacial energy. The theoretical description of this process is of central importance to materials design, yet remains controversial. In order to directly compare experiment to theoretical predictions, low solid volume fraction PbSn alloys were coarsened in a microgravity environment aboard the International Space Station (ISS) as part of the Coarsening in Solid Liquid Mixtures (CSLM) project. PbSn samples with solid volume fractions of 15%, 20% and 30% were characterized in 2D and 3D using mechanical serial sectioning. The systems were observed in the self-similar regime predicted by theory and the particle size and particle density obeyed the temporal power laws predicted by theory. However, the magnitudes of the rate constants governing those temporal laws as well as the forms of the particle size distributions were not described well by theoretical predictions. Additionally, in the 30% solid volume fraction system, the higher volume fraction results in a non-spherical particle shape and a more closely packed spatial distribution. The presence of slow particle motion induced by vibrations on the ISS is presented as an explanation for this discrepancy. To model the effect of this particle motion, the Akaiwa-Voorhees multiparticle diffusion simulations are modified to treat coarsening in the presence of a small convection term, such as that of sedimentation, corresponding to low Peclet numbers. The simulations indicate that the particle size dependent velocity of the sedimentation increases the rate at which the system coarsens. This is due to the larger particles traveling farther than normal, resulting in them encountering more small particles, which favors their growth. Additionally, sedimentation resulted in broader PSDs with a peak located at the average particle size. When the simulations are modified to

  7. Solid/liquid lubrication of ceramics at elevated temperatures

    SciTech Connect

    Erdemir, A.; Erck, R.A.; Fenske, G.R.; Hong, H.

    1996-04-01

    This study investigates the effect of solid and liquid lubrication on friction and wear performance of silicon nitride (Si{sub 3}N{sub 4}) and cast iron. The solid lubricant was a thin silver film ({approx}2 {mu}m thick) produced on Si{sub 3}N{sub 4} by ion-beam-assisted deposition. A high-temperature polyol-ester-base synthetic oil served as the liquid lubricant. Friction and wear tests were performed with pin-on-disk and oscillating-slider wear test machines at temperatures up to 300{degrees}C. Without the silver films, the friction coefficients of Si{sub 3}N{sub 4}/Si{sub 3}N{sub 4} test pairs were 0.05 to 0.14, and the average wear rates of Si{sub 3}N{sub 4} pins were {approx}5 x 10{sup -8} mm{sup 3} N{sup -1}. The friction coefficients of Si{sub 3}N{sub 4}/cast iron test pairs ranged from 0.08 to 0.11, depending on test temperature. The average specific wear rates of cast iron pins were {approx}3 x 10{sup -7} mm{sup 3} N{sup -1} m{sup -1}. However, simultaneous use of the solid-lubricant silver and synthetic oil on the sliding surfaces reduced friction coefficients to 0.02 to 0.08. Moreover, the wear of Si{sub 3}N{sub 4} pins and silver-coated Si{sub 3}N{sub 4} disks was so low that it was difficult to assess by a surface profilometer. The wear rates of cast iron pins were {approx}7 x 10{sup -9} mm{sup 3} N{sup -1} m{sup -1} up to 250{degrees}C, but showed a tendency to increase slightly at much higher temperatures. In general, the test results demonstrated that the solid/liquid lubrication of ceramic and/or metallic components is both feasible and effective in controlling friction and wear.

  8. Atomistic simulations of the solid-liquid transition of 1-ethyl-3-methyl imidazolium bromide ionic liquid.

    PubMed

    Feng, Haijun; Zhou, Jian; Qian, Yu

    2011-10-14

    Achieving melting point around room temperature is important for applications of ionic liquids. In this work, molecular dynamics simulations are carried out to investigate the solid-liquid transition of ionic liquid 1-ethyl-3-methyl imidazolium bromide ([emim]Br) by direct heating, hysteresis, void-nucleation, sandwich, and microcanonical ensemble approaches. Variations of the non-bonded energy, density, diffusion coefficient, and translational order parameter of [emim]Br are analyzed as a function of temperature, and a coexisting solid-liquid system is achieved in the microcanonical ensemble method. The melting points obtained from the first three methods are 547 ± 8 K, 429 ± 8 K, and 370 ± 6 K; while for the sandwich method, the melting points are 403 ± 4 K when merging along the x-axis by anisotropic isothermal-isobaric (NPT) ensemble, 393 ± 4 K when along the y-axis by anisotropic NPT ensemble, and 375 ± 4 K when along the y-axis by isotropic NPT ensemble. For microcanonical ensemble method, when the slabs are merging along different directions (x-axis, y-axis, and z-axis), the melting points are 364 ± 3 K, 365 ± 3 K, and 367 ± 3 K, respectively, the melting points we get by different methods are approximately 55.4%, 21.9%, 5.1%, 14.5%, 11.6%, 6.5%, 3.4%, 3.7%, and 4.3% higher than the experimental value of 352 K. The advantages and disadvantages of each method are discussed. The void-nucleation and microcanonical ensemble methods are most favorable for predicting the solid-liquid transition. PMID:22010721

  9. TOPICAL REVIEW: Sensors and actuators based on surface acoustic waves propagating along solid liquid interfaces

    NASA Astrophysics Data System (ADS)

    Lindner, Gerhard

    2008-06-01

    The propagation of surface acoustic waves (SAWs) along solid-liquid interfaces depends sensitively on the properties of the liquid covering the solid surface and may result in a momentum transfer into the liquid and thus a propulsion effect via acoustic streaming. This review gives an overview of the design of different SAW devices used for the sensing of liquids and the basic mechanisms of the interaction of SAWs with overlaying liquids. In addition, applications of devices based on these phenomena with respect to touch sensing and the measurement of liquid properties such as density, viscosity or the composition of mixed liquids are described, including microfabricated as well as macroscopic devices made from non-piezoelectric materials. With respect to the rapidly growing field of acoustic streaming applications, recent developments in the movement of nanolitre droplets on a single piezoelectric chip, the rather macroscopic approaches to the acoustic pumping of liquids in channels and recent attempts at numerical simulations of acoustic streaming are reported.

  10. Adsorption of hydrophobin/β-casein mixtures at the solid-liquid interface.

    PubMed

    Tucker, I M; Petkov, J T; Penfold, J; Thomas, R K; Cox, A R; Hedges, N

    2016-09-15

    The adsorption behaviour of mixtures of the proteins β-casein and hydrophobin at the hydrophilic solid-liquid surface have been studied by neutron reflectivity. The results of measurements from sequential adsorption and co-adsorption from solution are contrasted. The adsorption properties of protein mixtures are important for a wide range of applications. Because of competing factors the adsorption behaviour of protein mixtures at interfaces is often difficult to predict. This is particularly true for mixtures containing hydrophobin as hydrophobin possesses some unusual surface properties. At β-casein concentrations ⩾0.1wt% β-casein largely displaces a pre-adsorbed layer of hydrophobin at the interface, similar to that observed in hydrophobin-surfactant mixtures. In the composition and concentration range studied here for the co-adsorption of β-casein-hydrophobin mixtures the adsorption is dominated by the β-casein adsorption. The results provide an important insight into how the competitive adsorption in protein mixtures of hydrophobin and β-casein can impact upon the modification of solid surface properties and the potential for a wide range of colloid stabilisation applications. PMID:27288573

  11. Tunable synergism/antagonism in a mixed nonionic/anionic surfactant layer at the solid/liquid interface.

    PubMed

    Lu, Shaohua; Somasundaran, Ponisseril

    2008-04-15

    The use of mixed surfactants for modification of solid surfaces is important for many applications, since beneficial synergism often occurs depending on the surfactant type and mixing conditions. Systematical information on the properties of surfactant mixtures at the solid/liquid interface can be helpful for optimizing the interactions between the surfactants and then their corresponding performance. In this work, a nonionic/anionic surfactant combination, n-dodecyl beta-d-maltoside (DM) and sodium dodecyl sulfonate (SDS), was selected for the study of adsorption on an oxide solid, alumina. Interestingly, the mixture of the two surfactants with opposite pH-dependence of adsorption on alumina exhibits some unique synergistic or antagonistic features that were found to be tunable in the region of pH 4-10. In addition, the DM/SDS molar ratio in the adsorbed layer was found to decrease with concentration in the saturated region at all the pH and mixing ratios tested. The decrease is attributed to the monomer concentration changes in solution due to the difference in surface activities of the two surfactants. The tunable features of this mixture at the solid/liquid interface provide a way to optimize the properties by changing the mixing conditions. This can be valuable in many applications, such as enhanced oil recovery, flotation, and solubilization. PMID:18324849

  12. Modeling the solid-liquid phase transition in saturated triglycerides

    NASA Astrophysics Data System (ADS)

    Pink, David A.; Hanna, Charles B.; Sandt, Christophe; MacDonald, Adam J.; MacEachern, Ronald; Corkery, Robert; Rousseau, Dérick

    2010-02-01

    We investigated theoretically two competing published scenarios for the melting transition of the triglyceride trilaurin (TL): those of (1) Corkery et al. [Langmuir 23, 7241 (2007)], in which the average state of each TL molecule in the liquid phase is a discotic "Y" conformer whose three chains are dynamically twisted, with an average angle of ˜120° between them, and those of (2) Cebula et al. [J. Am. Oil Chem. Soc. 69, 130 (1992)], in which the liquid-state conformation of the TL molecule in the liquid phase is a nematic h∗-conformer whose three chains are in a modified "chair" conformation. We developed two competing models for the two scenarios, in which TL molecules are in a nematic compact-chair (or "h") conformation, with extended, possibly all-trans, chains at low-temperatures, and in either a Y conformation or an h∗ conformation in the liquid state at temperatures higher than the phase-transition temperature, T∗=319 K. We defined an h-Y model as a realization of the proposal of Corkery et al. [Langmuir 23, 7241 (2007)], and explored its predictions by mapping it onto an Ising model in a temperature-dependent field, performing a mean-field approximation, and calculating the transition enthalpy ΔH. We found that the most plausible realization of the h-Y model, as applied to the solid-liquid phase transition in TL, and likely to all saturated triglycerides, gave a value of ΔH in reasonable agreement with the experiment. We then defined an alternative h-h∗ model as a realization of the proposal of Cebula et al. [J. Am. Oil Chem. Soc. 69, 130 (1992)], in which the liquid phase exhibits an average symmetry breaking similar to an h conformation, but with twisted chains, to see whether it could describe the TL phase transition. The h-h∗ model gave a value of ΔH that was too small by a factor of ˜3-4. We also predicted the temperature dependence of the 1132 cm-1 Raman band for both models, and performed measurements of the ratios of three TL Raman

  13. Nonlinear vibrational spectroscopic studies of molecular interaction and charging behavior at solid/liquid interfaces

    NASA Astrophysics Data System (ADS)

    Zhang, Luning

    Solid-liquid interfaces have been the focus of different communities of scientists due to its importance in industrial applications and chemical processes in nature. Molecular interactions and surface charges affect the physicochemical properties of these interfaces and a thorough understanding is still lacking now. This thesis describes our work in studying several model solid-liquid interfaces using sum-frequency vibrational spectroscopy. Through the studies of interfacial vibrational spectra, we hope to gain better understanding of molecular interactions in competitive adsorption process and also surface charging behavior at different pH and salt concentrations. We start by studying alcohol-water mixture and the adsorption behavior at both hydrophilic and hydrophobic surfaces. In both cases, alcohol adsorbs preferentially from water. The tendency for water to form strong hydrogen-bonding network is the driving force for preferential adsorption of alcohol. We proposed two different interfacial molecular structures on hydrophilic and hydrophobic surfaces. We move on to study the interaction of pure water with a solid surface. Single crystal alumina is used as a model system. At different pH, the surface can undergo protonation and deprotonation reactions and accumulates surface charge. Both the hydrogen-bonding with water and the surface field created by surface charge can affect interfacial water structure. Combining the information obtained with intensity and phase spectra, we find water molecules have two types of bonding within the interfacial layer: weakly hydrogen-bonded species near 3450 cm-1 that does not flip with switching surface charge, and strongly hydrogen-bonded species at 3200 cm-1 that readily flips with switching surface field. One other system we have studied is nanoporous silica-water interface. We found that signal from interfacial water is reduced due to the porous nature of the film. The water spectral features tell us about the interfacial

  14. Determination of pesticides in lettuce using solid-liquid extraction with low temperature partitioning.

    PubMed

    Costa, Anna I G; Queiroz, Maria E L R; Neves, Antônio A; de Sousa, Flaviane A; Zambolim, Laércio

    2015-08-15

    This work describes the optimization and validation of a method employing solid-liquid extraction with low temperature partitioning (SLE/LTP) together with analysis by gas chromatography with electron capture detection (GC/ECD) for the determination of nine pesticides (chlorothalonil, methyl parathion, procymidone, endosulfan, iprodione, λ-cyhalothrin, permethrin, cypermethrin, and deltamethrin) in lettuce. The method was found to be selective, accurate, and precise, with means recovery values in the range of 72.3-103.2%, coefficients of variation ⩽ 12%, and detection limits in the range 0.4-37 μg kg(-1). The matrix components significantly influence the chromatographic response of the analytes (above 10%). The optimized and validated method was applied to determine the residual concentrations of the fungicides iprodione and procymidone that had been applied to field crops of lettuce. The maximum residual concentrations of the pesticides in the lettuce samples were 13.6 ± 0.4 mg kg(-1) (iprodione) and 1.00 ± 0.01 mg kg(-1) (procymidone), on the day after application of the products. PMID:25794722

  15. Dynamic covalent chemistry of bisimines at the solid/liquid interface monitored by scanning tunnelling microscopy

    NASA Astrophysics Data System (ADS)

    Ciesielski, Artur; El Garah, Mohamed; Haar, Sébastien; Kovaříček, Petr; Lehn, Jean-Marie; Samorì, Paolo

    2014-11-01

    Dynamic covalent chemistry relies on the formation of reversible covalent bonds under thermodynamic control to generate dynamic combinatorial libraries. It provides access to numerous types of complex functional architectures, and thereby targets several technologically relevant applications, such as in drug discovery, (bio)sensing and dynamic materials. In liquid media it was proved that by taking advantage of the reversible nature of the bond formation it is possible to combine the error-correction capacity of supramolecular chemistry with the robustness of covalent bonding to generate adaptive systems. Here we show that double imine formation between 4-(hexadecyloxy)benzaldehyde and different α,ω-diamines as well as reversible bistransimination reactions can be achieved at the solid/liquid interface, as monitored on the submolecular scale by in situ scanning tunnelling microscopy imaging. Our modular approach enables the structurally controlled reversible incorporation of various molecular components to form sophisticated covalent architectures, which opens up perspectives towards responsive multicomponent two-dimensional materials and devices.

  16. Characterization of Solid Liquid Suspensions Utilizing Non-Invasive Ultrasonic Measurements

    SciTech Connect

    Panetta, P.D.; Tucker, B.; Ahmed, S.; Pappas, R.A.

    2004-03-31

    Rapid, on-line characterization of the particle size and concentration of moderate to highly concentrated slurries is required for efficient waste remediation at the DOE complexes. This paper discusses the advancements achieved under the Environmental Management Science Program to accurately characterize high-level waste at the high concentrations expected at the DOE complexes. In addition, the results are applicable to efficient process measurement and control in many chemical and pharmaceutical manufacturing processes. Existing methods for determining the particle size and concentration of non-dilute slurries based on ultrasonic attenuation can become inaccurate due to the complex interactions of ultrasonic waves with the constituents of the slurries and the necessity for very careful transducer alignment. Two measurements that help to overcome these difficulties are the ultrasonic backscattering and diffuse field. The backscattering measurement is attractive because viscous, thermal and inertial effects have small contributions to the backscattering. In addition, the backscattering theories are simpler than attenuation theories and lend themselves to more stable inversion processes. Furthermore, the measurements of backscattering measurement do not require long travel distances and can be made with a single transducer thus eliminating alignment problems. We will present ultrasonic measurements and theoretical comparisons on solid liquid suspensions designed to elucidate the particle size and concentration at high concentration relevant to the high level waste at the DOE complexes.

  17. Step free energies at faceted solid-liquid interfaces from equilibrium molecular dynamics simulations.

    PubMed

    Frolov, T; Asta, M

    2012-12-01

    In this work a method is proposed for computing step free energies for faceted solid-liquid interfaces based on atomistic simulations. The method is demonstrated in an application to (111) interfaces in elemental Si, modeled with the classical Stillinger-Weber potential. The approach makes use of an adiabatic trapping procedure, and involves simulations of systems with coexisting solid and liquid phases separated by faceted interfaces containing islands with different sizes, for which the corresponding equilibrium temperatures are computed. We demonstrate that the calculated coexistence temperature is strongly affected by the geometry of the interface. We find that island radius is inversely proportional to superheating, allowing us to compute the step free energy by fitting simulation data within the formalism of classical nucleation theory. The step free energy value is computed to be γ(st) = 0.103 ± 0.005 × 10(-10) J/m. The approach outlined in this work paves the way to the calculation of step free energies relevant to the solidification of faceted crystals from liquid mixtures, as encountered in nanowire growth by the vapor-liquid-solid mechanism and in alloy casting. The present work also shows that at low undercoolings the Stillinger-Weber interatomic potential for Si tends to crystallize in the wurtzite, rather than the diamond-cubic structure. PMID:23231218

  18. Solid Liquid Interdiffusion Bonding of Zn4Sb3 Thermoelectric Material with Cu Electrode

    NASA Astrophysics Data System (ADS)

    Lin, Y. C.; Lee, K. T.; Hwang, J. D.; Chu, H. S.; Hsu, C. C.; Chen, S. C.; Chuang, T. H.

    2016-06-01

    The ZnSb intermetallic compound may have thermoelectric applications because it is low in cost and environmentally friendly. In this study, a Zn4Sb3 thermoelectric element coated with a Ni barrier layer and a Ag reaction layer was bonded with a Ag-coated Cu electrode using a Ag/Sn/Ag solid-liquid interdiffusion bonding process. The results indicated that a Ni5Zn21 intermetallic phase formed easily at the Zn4Sb3/Ni interface, leading to sound adhesion. In addition, Sn film was found to react completely with the Ag layer to form a Ag3Sn intermetallic layer having a melting point of 480°C. The resulting Zn4Sb3 thermoelectric module can be applied at the optimized operation temperature (400°C) of Zn4Sb3 material as a thermoelectric element. The bonding strengths ranged from 14.9 MPa to 25.0 MPa, and shear tests revealed that the Zn4Sb3/Cu-joints fractured through the interior of the thermoelectric elements.

  19. Solid-liquid phase equilibrium for binary Lennard-Jones mixtures

    NASA Astrophysics Data System (ADS)

    Hitchcock, Monica R.; Hall, Carol K.

    1999-06-01

    Solid-liquid phase diagrams are calculated for binary mixtures of Lennard-Jones spheres using Monte Carlo simulation and the Gibbs-Duhem integration technique of Kofke. We calculate solid-liquid phase diagrams for the model Lennard-Jones mixtures: argon-methane, krypton-methane, and argon-krypton, and compare our simulation results with experimental data and with Cottin and Monson's recent cell theory predictions. The Lennard-Jones model simulation results and the cell theory predictions show qualitative agreement with the experimental phase diagrams. One of the mixtures, argon-krypton, has a different phase diagram than its hard-sphere counterpart, suggesting that attractive interactions are an important consideration in determining solid-liquid phase behavior. We then systematically explore Lennard-Jones parameter space to investigate how solid-liquid phase diagrams change as a function of the Lennard-Jones diameter ratio, σ11/σ22, and well-depth ratio, ɛ11/ɛ22. This culminates in an estimate of the boundaries separating the regions of solid solution, azeotrope, and eutectic solid-liquid phase behavior in the space spanned by σ11/σ22 and ɛ11/ɛ22 for the case σ11/σ22<0.85.

  20. Influence of Melt Convection on Solid-Liquid Interface Under Terrestrial and Reduced Gravity Environments

    NASA Technical Reports Server (NTRS)

    Glicksman, M. E.

    1985-01-01

    Solidification and crystal growth processes involve thermal and solutal gradients within a molten phase. In the presence of gravity, such gradients result in convective flows which interact with diffusion fields at the solid-liquid interface. Dendritic growth kinetics was studied in transparent model systems which freeze similarily to most metals. Succinonitrile shows a strong influence of convection at supercoolings below about 1K. Fluid flows adjacent to solid-liquid interfaces and the behavior of shear flows in vertical annular geometries are studied. Novel low-frequency eigenstates were discovered and classified as coupled modes, for their involvement with interfacial deformation coupled to the fluid flow, and are unknown in systems without deformable interfaces. The dependence of coupled convection modes on interfacial geometry, gravity, fluid properties, and transformation characteristics studied for several annual flow arrangements with nominally pure solid-liquid systems.

  1. Critère de fatigue polycyclique pour des matériaux anisotropes : application aux monocristaux

    NASA Astrophysics Data System (ADS)

    Cano, Florian; Constantinescu, Andrei; Maitournam, Habibou

    2004-02-01

    The high-cycle fatigue criteria based on a macroscopic-mesoscopic scale interpretation, initiated by Dang Van, were used essentially for polycrystalline materials. In the existing criteria the material isotropy at both mesoscopic and macroscopic scales plays a key role. The purpose of this paper is to revisit the macroscopic to mesoscopic fatigue approach taking into account the material anisotropy and some results obtained by Bui. The possible applications are some anisotropic steels or monocrystalline structures such as stitanium turbine blades. To cite this article: F. Cano et al., C. R. Mecanique 332 (2004).

  2. Transport Electronique Dans Les Super Reseaux : Applications Aux Détecteurs Infrarouges à Grandes Longueur D'onde

    NASA Astrophysics Data System (ADS)

    Lhuillier, Emmanuel

    2010-11-01

    The low flux infrared imaging needs performant high wavelength detectors. Quantum Well Infrared Photodetectors (QWIP), thanks to the maturity of GaAs, the possibility to adjust the detected wavelength on a large range and to realize large uniform matrix are good candidate for such applications. In order to validate this interest, we have performed an electro-optic characterization of a 15{μ}m sample. These measurements have been used to simulate the performance of a camera based on this QWIP and used in a low infrared photons flux scenario. We predict that this QWIP would succeed. Nevertheless these simulations also underline the detrimental role of the dark current. Thus we have developed a simulation tool based on a hoping approach between localized states, which provide us a better understanding of the transport in these heterostructures. The code has in particular underlines the role plays by the electron -ionized impurities interaction, which make the dark current very sensitive to the doping profile. Using this tool we have designed new structures, with optimized doping profile, in which the scattering rate has been decreased by a factor two. Moreover we have identified a quantum origin to the plateau shape of the I(V) curve. This code is more generally a useful simulation tool for the transport in hétérostructures. The influence of growth defects (non ideal interface and disorder) has been quantized and we have performed the first evaluation of The R0A in a THz QCD. Finally non local transport effects have been investigated. Saw teeth observation on the I(V) curves have been modeled and their influence on the detectivty estimated.

  3. Abatement of ammonia emissions from swine lagoons using polymer enhanced solid-liquid separation

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A study was conducted to determine the effects of solid-liquid separation of liquid swine manure on ammonia emissions from lagoons. This determination was done at full-scale in two contiguous swine production units that had similar animal production management. One of these units was maintained as a...

  4. Solid-Liquid and Liquid-Liquid Mixing Laboratory for Chemical Engineering Undergraduates

    ERIC Educational Resources Information Center

    Pour, Sanaz Barar; Norca, Gregory Benoit; Fradette, Louis; Legros, Robert; Tanguy, Philippe A.

    2007-01-01

    Solid-liquid and liquid-liquid mixing experiments have been developed to provide students with a practical experience on suspension and emulsification processes. The laboratory focuses on the characterization of the process efficiency, specifically the influence of the main operating parameters and the effect of the impeller type. (Contains 2…

  5. Versatile Side-Illumination Geometry for Tip-Enhanced Raman Spectroscopy at Solid/Liquid Interfaces.

    PubMed

    Martín Sabanés, Natalia; Driessen, Leonie M A; Domke, Katrin F

    2016-07-19

    In situ characterization of surfaces with tip-enhanced Raman spectroscopy (TERS) provides chemical and topographic information with high spatial resolution and submonolayer chemical sensitivity. To further the versatility of the TERS approach toward more complex systems such as biological membranes or energy conversion devices, adaptation of the technique to solid/liquid working conditions is essential. Here, we present a home-built side-illumination TERS setup design based on a commercial scanning tunneling microscope (STM) as a versatile, cost-efficient solution for TERS at solid/liquid interfaces. Interestingly, the results obtained from showcase resonant dye and nonresonant thiophenol monolayers adsorbed on Au single crystals suggest that excitation beam aberrations due to the presence of the aqueous phase are small enough not to limit TER signal detection. The STM parameters are found to play a crucial role for solid/liquid TERS sensitivity. Raman enhancement factors of 10(5) at μW laser power demonstrate the great potential the presented experimental configuration holds for solid/liquid interfacial spectroscopic studies. PMID:27299508

  6. Investigation of surface charge density on solid-liquid interfaces by modulating the electrical double layer.

    PubMed

    Moon, Jong Kyun; Song, Myung Won; Pak, Hyuk Kyu

    2015-05-20

    A solid surface in contact with water or aqueous solution usually carries specific electric charges. These surface charges attract counter ions from the liquid side. Since the geometry of opposite charge distribution parallel to the solid-liquid interface is similar to that of a capacitor, it is called an electrical double layer capacitor (EDLC). Therefore, there is an electrical potential difference across an EDLC in equilibrium. When a liquid bridge is formed between two conducting plates, the system behaves as two serially connected EDLCs. In this work, we propose a new method for investigating the surface charge density on solid-liquid interfaces. By mechanically modulating the electrical double layers and simultaneously applying a dc bias voltage across the plates, an ac electric current can be generated. By measuring the voltage drop across a load resistor as a function of bias voltage, we can study the surface charge density on solid-liquid interfaces. Our experimental results agree very well with the simple equivalent electrical circuit model proposed here. Furthermore, using this method, one can determine the polarity of the adsorbed state on the solid surface depending on the material used. We expect this method to aid in the study of electrical phenomena on solid-liquid interfaces. PMID:25923410

  7. Bionic optical imaging system with aspheric solid-liquid mixed variable-focus lens

    NASA Astrophysics Data System (ADS)

    Du, Jia-Wei; Wang, Xuan-Yin; Liang, Dan

    2016-02-01

    A bionic optical imaging system with an aspheric solid-liquid mixed variable-focus lens was designed and fabricated. The entire system mainly consisted of a doublet lens, a solid-liquid mixed variable-focus lens, a connecting part, and a CCD imaging device. To mimic the structure of the crystalline lens, the solid-liquid mixed variable-focus lens consisted of a polydimethylsiloxane (PDMS) lens, a polymethyl methacrylate lens, and the liquid of ethyl silicone oil. By pumping liquid in or out of the cavity using a microinjector, the curvatures of the front and rear surfaces of the PDMS lens were varied, resulting in a change of focal length. The overall structure of the system was presented, as well as a detailed description of the solid-liquid mixed variable-focus lens, material, and fabrication process. Under different injection volumes, the deformation of the PDMS lens was measured and simulated, pictures were captured, and the optical performance was analyzed in simulations and experiments. The focal length of the system ranged from 25.05 to 14.61 mm, and the variation of the diopter was 28.5D, which was larger than that of the human eye.

  8. All about Solids, Liquids & Gases. Physical Science for Children[TM]. Schlessinger Science Library. [Videotape].

    ERIC Educational Resources Information Center

    2000

    In All About Solids, Liquids and Gases, young students will be introduced to the three common forms of matter. They'll learn that all things are made up of tiny particles called atoms and that the movement of these particles determines the form that matter takes. In solids, the particles are packed tightly together and move very little. The…

  9. Enhanced solid-liquid separation of dairy manure with natural flocculants

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Natural flocculants have potential to replace the use of synthetic flocculants used for enhanced solid-liquid separation of livestock effluents, especially with increased cost of energy and renewed interest on organic farming systems. We conducted a study to determine the effectiveness of natural fl...

  10. Binary Solid-Liquid Phase Diagram of Phenol and t-Butanol: An Undergraduate Physical Chemistry Experiment

    ERIC Educational Resources Information Center

    Xu, Xinhua; Wang, Xiaogang; Wu, Meifen

    2014-01-01

    The determination of the solid-liquid phase diagram of a binary system is always used as an experiment in the undergraduate physical chemistry laboratory courses. However, most phase diagrams investigated in the lab are simple eutectic ones, despite the fact that complex binary solid-liquid phase diagrams are more common. In this article, the…

  11. Occurrence and solid-liquid partition of sulfonated naphthalene-formaldehyde condensates in the aquatic environment.

    PubMed

    Lange, Frank T; Merklinger, Michael; Wenz, Michael; Brauch, Heinz-J; Lehmann, Markus; Pinter, Istvan

    2005-03-15

    Sulfonated naphthalene-formaldehyde condensates (SNFC) are high production volume chemicals used in a variety of applications, for example, as concrete plasticizers, tanning agents, or dye dispersants. They enter the aquatic environment primarily by the wastewater path. The occurrence and fate of the monomers, which are different isomers of mono- and disulfonated naphthalene, was intensively investigated in previous studies. However, the environmental fate of the persistent higher molecular SNFC is so far widely unknown. This paper describes an ultrasonic extraction under alkaline conditions, followed by ion-pair HPLC with fluorescence detection for the analysis of SNFC oligomers from solid environmental matrixes such as sewage sludge, suspended solids, and river sediments. Limits of quantification of about 0.1 mg kg-1 d.m. were well below the measured concentrations in environmental samples. SNFC were adsorbed to suspended solids and river sediments in three major German rivers (Rhine, Neckar, and Danube) in concentrations typically up to several mg kg(-1) d.m. A total content of about 4 g kg(-1) d.m. was measured in a sewage sludge of a municipal wastewater treatment plant, which receives wastewater from a textile dyeing plant. Furthermore, the first quantitative field data on the partition of SNFC and their monomers between the aqueous phase and solid environmental compartments are presented. Solid-liquid partition coefficients (Kd) of oligomers with a chain-length ranging from three to six naphthalenesulfonate units were derived from the analysis of corresponding wastewater and sewage sludge samples and from suspended solids and river water samples, respectively. Determined Kd values were in the range from 10(2) to 10(4) L kg(-1). PMID:15819205

  12. Adsorption of R-OH molecules on TiO2 surfaces at the solid-liquid interface.

    PubMed

    Sánchez, Verónica M; de la Llave, Ezequiel; Scherlis, Damian A

    2011-03-15

    The exploration of TiO2 surface reactivity from first-principles calculations has been almost always limited to the gas phase, even though most of the chemically relevant applications of this interface involve the solid-liquid boundary. The reason for this limitation is the complexity of the solid-liquid interface, which poses a serious challenge to standard ab initio methodologies as density functional theory (DFT). In this work we study the interaction of H2O, CH3OH, H2O2, and HCO2H with anatase (101) and rutile (110) surfaces in aqueous solution, employing a continuum solvation model in a DFT framework in periodic boundary conditions [ J. Chem. Phys. 2009 , 131 , 174108 ]. Different adsorption configurations were analyzed, examining the effect of the first water monolayer explicitly included in the simulation. For water and methanol, molecular adsorption was found to be the most stable in the presence of the solvent, while for hydrogen peroxide the preferred configuration depended on the surface. The explicit inclusion of the first water monolayer turns out to be important since it may play a role in the stabilization of the adsorbates at the interface. In general, the slightly positive adsorption energy values obtained (with respect to water) suggest that CH3OH and H2O2 will poorly adsorb from an aqueous solution at the titania surface. Among the three species investigated other than water, the formic acid was the only one to exhibit a higher affinity for the surface than H2O. PMID:21314168

  13. Solid-liquid separation for liquefied coal industries. Final report

    SciTech Connect

    Tiller, F.M.; Leu, W.

    1984-07-01

    This book has been written for engineers concerned with separation processes related to liquefied coal slurries. Difficulties in removing mineral residues and unconverted carbon represent a major obstacle to economic production of liquefied coal products. Reactor slurries in which hydrogenation has been used to upgrade coal generally contain 5 to 10 weight percents of solids which must be removed. Various kinds of equipment employed for particulate removal include rotary drum pressure, candle, and leaf filters, solid bowl centrifuges, hydrocyclones, and critical solvent de-ashers. Although emphasis has been given to filtration of solvent refined coal, much of the material is of a fundamental character and is applicable to other fields. Analysis of filtration data requires an understanding of the principles of frictional flow through compressible beds of particulates. Much of the analysis appearing in the literature must be carefully evaluated as errors and misinterpretations abound.

  14. Flowing Foam: T1 events and solid-liquid transitions.

    NASA Astrophysics Data System (ADS)

    Dennin, Michael

    2005-11-01

    Flowing aqueous foam is found in many applications ranging from oil recovery, to fire fighting, to spreading shaving cream. Aqueous foam consists of gas bubbles with liquid walls. One of the striking features of foam is that despite being composed entirely of fluids, its mechanical properties are either those of a solid (elastic response) or fluid (viscous flow), depending on the nature of the applied stress and strains. We study the transition between these two regimes using a model foam system: bubble rafts. Bubble rafts are a single layer of bubbles floating on the air-water surface. This allows us to track the motion of all the bubbles during flow. In this talk, we will present two main results. First, we will discuss the observation of the coexistence between a solid-like and fluid-like state during flow. Second, we will discuss the role played by nonlinear, topological rearrangements, known as T1 events, in determining the mechanical response of the system.

  15. Numerical simulation of solid liquid interface behavior during continuous strip casting process.

    PubMed

    Lee, Changbum; Yoon, Wooyoung; Shin, Seungwon; Lee, Jaewoo; Jang, Bo-Yun; Kim, Joonsoo; Ahn, Youngsoo; Lee, Jinseok

    2013-05-01

    A new metal-strip-casting process called continuous strip-casting (CSC) has been developed for making thin metal strips. A numerical simulation model to help understand solid-liquid interface behavior during CSC has been developed and used to identify the solidification morphologies of the strips and to determine the optimum processing conditions. In this study, we used a modified level contour reconstruction method (LCRM) and the sharp interface method to modify interface tracking, and performed a simulation analysis of the CSC process. The effects of process parameters such as heat-transfer coefficient and extrusion velocity on the behavior of the solid-liquid interface were estimated and used to improve the apparatus. A Sn (Tin) plate of dimensions 200 x 50 x 1 mm3 was successfully produced by CSC for a heat-transfer coefficient of 104 W/m2 K and an extrusion velocity of 0.2 m/s. PMID:23858856

  16. Thermodynamic and rheological properties of solid-liquid systems in coal processing

    SciTech Connect

    Kabadi, V.N.; Ilias, S.

    1992-01-01

    In this report we present two data sets that have been compiled to assist in the model developments for solid-liquid equilibria and viscosities of coal derived systems. The first one is on vapor pressures of solid aromatics and the second one consists of viscosities of pure model compounds and some mixtures. These databanks are ready for usage in model development and are summarized in Tables 1 and 2. Literature is being searched to compile similar data for high pressure liquid compressibilities, liquid and solid heat capacities and solid-liquid equilibria for model compound systems. Literature search is also containing to investigate available viscosity models. Once this is completed a few models will be selected for evaluation and consideration as candidates for extension to coal liquids.

  17. Performance analysis on solid-liquid mixed flow in a centrifugal pump

    NASA Astrophysics Data System (ADS)

    Ning, C.; Wang, Y.

    2016-05-01

    In order to study the solid-liquid mixed flow hydraulic characteristics of centrifugal pump, the Pro/E software was used for three-dimensional modeling of centrifugal pump chamber. By using the computational fluid dynamics software CFX, the numerical simulation calculation of solid-liquid two-phase flow within whole flow passage of centrifugal pump was conducted. Aim at different particle diameters, the Reynolds-averaged N-S equations with the RNG k-Ɛ turbulence model and SIMPLEC algorithm were used to simulate the two-phase flow respectively on the condition of different volume fraction. The influence of internal flow characteristic on pump performance was analyzed. On the conditions of different particle diameter and different volume fraction, the turbulence kinetic energy and particle concentration are analyzed. It can be found that the erosion velocity ratio on the flow channel wall increases along with the increasing of the volume fraction

  18. Numerical formulation of composition segregation at curved solid-liquid interface during steady state solidification process

    NASA Technical Reports Server (NTRS)

    Wang, Jai-Ching

    1994-01-01

    The lateral solute segregation that results from a curved solid-liquid interface shape during steady state unidirectional solidification of a binary alloy system has been studied both analytically and numerically by Coriell, Bosivert, Rehm, and Sekerka. The system under their study is a two dimensional rectangular system. However, most real growth systems are cylindrical systems. Thus, in a previous study, we have followed Coriell etc. formalism and obtained analytical results for lateral solute segregation for an azimuthal symmetric cylindrical binary melt system during steady state solidification process. The solid-liquid interface shape is expressed as a series combination of Bessel functions. In this study a computer program has been developed to simulate the lateral solute segregation.

  19. A new continuous device to perform S-L-G photocatalytic studies. [Solid-Liquid-Gas

    SciTech Connect

    Aguado, M.A.; Gimenez, J.; Simarro, R.; Cervera-March, S. )

    1992-07-01

    A new experimental device to carry out solid-liquid-gas photocatalytic studies is presented. It can operate as a continuous system with respect to both the gas and the liquid phase. The solid photocatalyst is held inside the system and is continuously recycled through it to enable the separation of the spent liquid. Steady values of liquid and gas composition as well as temperature and fluidodynamic variables can be set and controlled.

  20. Note: Sample cells to investigate solid/liquid interfaces with neutrons

    SciTech Connect

    Rennie, Adrian R. Hellsing, Maja S.; Lindholm, Eric; Olsson, Anders

    2015-01-15

    The design of sample cells to study solid/liquid interfaces by neutron reflection is presented. Use of standardized components and a modular design has allowed a wide range of experiments that include grazing incidence scattering and conventional small-angle scattering. Features that reduce background scattering are emphasized. Various flow arrangements to fill and replenish the liquid in the cell as well as continuous stirring are described.

  1. Correlation among the laser-induced breakdown thresholds in solids, liquids, and gases.

    PubMed

    Bettis, J R

    1992-06-20

    A simple expression is developed that permits a correlation among laser-induced breakdown thresholds in solids, liquids, and gases. It is shown that the breakdown thresholds for the bulk of solid dielectrics, linear liquids, and gases all follow a linear fit to the expression N(2/3)/(n(2) - 1), where N is the atomic number density and n is the refractive index. The gas breakdown threshold versus pressure is compared with the predicted dependence. PMID:20725310

  2. Interaction of Porosity with an Advancing Solid/Liquid Interface: a Real-Time Investigation

    NASA Technical Reports Server (NTRS)

    Sen, S.; Kaukler, W.; Catalina, A.; Stefanescu, D.; Curreri, P.

    1999-01-01

    Problems associated with formation of porosity during solidification continue to have a daily impact on the metal forming industry. Several past investigations have dealt with the nucleation and growth aspects of porosity. However, investigations related to the interaction of porosity with that of a solidification front has been limited mostly to organic analogues. In this paper we report on real time experimental observations of such interactions in metal alloys. Using a state of the art X-Ray Transmission Microscope (XTM) we have been able to observe and record the dynamics of the interaction. This includes distortion of the solid/liquid interface near a poro.sity, solute segr,egation patterns surrounding a porosity and the change in shape of the porosity during interaction with an advancing solid/liquid interface. Results will be presented for different Al alloys and growth conditions. The experimental data will be compared to theory using a recently developed 2D numerical model. The model employs a finite difference approach where the solid/liquid interface is defined through the points at which the interface intersects the grid lines. The transport variables are calculated at these points and the motion of the solidification front is determined by the magnitude of the transport variables. The model accounts for the interplay of the thermal and solutal field and the influence of capilarity to predict the shape of the solid/liquid interface with time in the vicinity of porosity. One can further calculate the perturbation of the solutal field by the presence of porosity in the melt.

  3. Effect of confinement on the solid-liquid coexistence of Lennard-Jones Fluid

    SciTech Connect

    Das, Chandan K.; Singh, Jayant K.

    2013-11-07

    The solid-liquid coexistence of a Lennard-Jones fluid confined in slit pores of variable pore size, H, is studied using molecular dynamics simulations. Three-stage pseudo-supercritical transformation path of Grochola [J. Chem. Phys. 120(5), 2122 (2004)] and multiple histogram reweighting are employed for the confined system, for various pore sizes ranging from 20 to 5 molecular diameters, to compute the solid-liquid coexistence. The Gibbs free energy difference is evaluated using thermodynamic integration method by connecting solid-liquid phases under confinement via one or more intermediate states without any first order phase transition among them. Thermodynamic melting temperature is found to oscillate with wall separation, which is in agreement with the behavior seen for kinetic melting temperature evaluated in an earlier study. However, thermodynamic melting temperature for almost all wall separations is higher than the bulk case, which is contrary to the behavior seen for the kinetic melting temperature. The oscillation founds to decay at around H = 12, and beyond that pore size dependency of the shift in melting point is well represented by the Gibbs-Thompson equation.

  4. Real-time single-molecule observations of proteins at the solid-liquid interface

    NASA Astrophysics Data System (ADS)

    Langdon, Blake Brianna

    Non-specific protein adsorption to solid surfaces is pervasive and observed across a broad spectrum of applications including biomaterials, separations, pharmaceuticals, and biosensing. Despite great interest in and considerable literature dedicated to the phenomena, a mechanistic understanding of this complex phenomena is lacking and remains controversial, partially due to the limits of ensemble-averaging techniques used to study it. Single-molecule tracking (SMT) methods allow us to study distinct protein dynamics (e.g. adsorption, desorption, diffusion, and intermolecular associations) on a molecule-by-molecule basis revealing the protein population and spatial heterogeneity inherent in protein interfacial behavior. By employing single-molecule total internal reflection fluorescence microscopy (SM-TIRFM), we have developed SMT methods to directly observe protein interfacial dynamics at the solid-liquid interface to build a better mechanistic understanding of protein adsorption. First, we examined the effects of surface chemistry (e.g. hydrophobicity, hydrogen-bonding capacity), temperature, and electrostatics on isolated protein desorption and interfacial diffusion for fibrinogen (Fg) and bovine serum albumin (BSA). Next, we directly and indirectly probed the effects of protein-protein interactions on interfacial desorption, diffusion, aggregation, and surface spatial heterogeneity on model and polymeric thin films. These studies provided many useful insights into interfacial protein dynamics including the following observations. First, protein adsorption was reversible, with the majority of proteins desorbing from all surface chemistries within seconds. Isolated protein-surface interactions were relatively weak on both hydrophobic and hydrophilic surfaces (apparent desorption activation energies of only a few kBT). However, proteins could dynamically and reversibly associate at the interface, and these interfacial associations led to proteins remaining on the

  5. Electrical impedance tomography spectroscopy method for characterising particles in solid-liquid phase

    NASA Astrophysics Data System (ADS)

    Zhao, Yanlin; Wang, Mi; Yao, Jun

    2014-04-01

    Electrical impedance tomography (EIT) is one of the process tomography techniques to provide an on-line non-invasive imaging for multiphase flow measurement. With EIT measurements, the images of impedance real part, impedance imaginary part, phase angle, and magnitude can be obtained. However, most of the applications of EIT in the process industries rely on the conductivity difference between two phases in fluids to obtain the concentration profiles. It is not common to use the imaginary part or phase angle due to the dominant change in conductivity or complication in the use of other impedance information. In a solid-liquid two phases system involving nano- or submicro-particles, characterisation of particles (e.g. particle size and concentration) have to rely on the measurement of impedance phase angle or imaginary part. Particles in a solution usually have an electrical double layer associated with their surfaces and can form an induced electrical dipole moment due to the polarization of the electrical double layer under the influence of an alternating electric field. Similar to EIT, electrical impedance spectroscopy (EIS) measurement can record the electrical impedance data, including impedance real part, imaginary part and phase angle (θ), which are caused by the polarization of the electrical double layer. These impedance data are related to the particle characteristics e.g. particle size, particle and ionic concentrations in the aqueous medium, therefore EIS method provides a capability for characterising the particles in suspensions. Electrical impedance tomography based on EIS measurement or namely, electrical impedance tomography spectroscopy (EITS) could image the spatial distribution of particle characteristics. In this paper, a new method, including test set-up and data analysis, for characterisation of particles in suspensions are developed through the experimental approach. The experimental results on tomographic imaging of colloidal particles

  6. Electrical impedance tomography spectroscopy method for characterising particles in solid-liquid phase

    SciTech Connect

    Zhao, Yanlin; Wang, Mi; Yao, Jun

    2014-04-11

    Electrical impedance tomography (EIT) is one of the process tomography techniques to provide an on-line non-invasive imaging for multiphase flow measurement. With EIT measurements, the images of impedance real part, impedance imaginary part, phase angle, and magnitude can be obtained. However, most of the applications of EIT in the process industries rely on the conductivity difference between two phases in fluids to obtain the concentration profiles. It is not common to use the imaginary part or phase angle due to the dominant change in conductivity or complication in the use of other impedance information. In a solid-liquid two phases system involving nano- or submicro-particles, characterisation of particles (e.g. particle size and concentration) have to rely on the measurement of impedance phase angle or imaginary part. Particles in a solution usually have an electrical double layer associated with their surfaces and can form an induced electrical dipole moment due to the polarization of the electrical double layer under the influence of an alternating electric field. Similar to EIT, electrical impedance spectroscopy (EIS) measurement can record the electrical impedance data, including impedance real part, imaginary part and phase angle (θ), which are caused by the polarization of the electrical double layer. These impedance data are related to the particle characteristics e.g. particle size, particle and ionic concentrations in the aqueous medium, therefore EIS method provides a capability for characterising the particles in suspensions. Electrical impedance tomography based on EIS measurement or namely, electrical impedance tomography spectroscopy (EITS) could image the spatial distribution of particle characteristics. In this paper, a new method, including test set-up and data analysis, for characterisation of particles in suspensions are developed through the experimental approach. The experimental results on tomographic imaging of colloidal particles

  7. Conception, elaboration et mise a l'essai d'un simulateur interactif permettant une approche modelisante: Application aux lois de la genetique mendelienne

    NASA Astrophysics Data System (ADS)

    Lasri, Abdel-Halim

    Dans cette recherche-developpement, nous avons concu, developpe et mis a l'essai un simulateur interactif pour favoriser l'apprentissage des lois probabilistes impliqees dans la genetique mendelienne. Cet environnement informatise devra permettre aux etudiants de mener des experiences simulees, utilisant les statistiques et les probebilites comme outils mathematiques pour modeliser le phenomene de la transmission des caracteres hereditaires. L'approche didactique est essentiellement orientee vers l'utilisation des methodes quantitatives impliquees dans l'experimentation des facteurs hereditaires. En incorporant au simulateur le principe de la "Lunette cognitive" de Nonnon (1986), l'etudiant fut place dans une situation ou il a pu synchroniser la perception de la representation iconique (concrete) et symbolique (abstraite) des lois probabilistes de Mendel. A l'aide de cet environnement, nous avons amene l'etudiant a identifier le(s) caractere(s) hereditaire(s) des parents a croiser, a predire les frequences phenotypiques probables de la descendance issue du croisement, a observer les resultats statistiques et leur fluctuation au niveau de l'histogramme des frequences, a comparer ces resultats aux predictions anticipees, a interpreter les donnees et a selectionner en consequence d'autres experiences a realiser. Les etapes de l'approche inductive sont privilegiees du debut a la fin des activites proposees. L'elaboration, du simulateur et des documents d'accompagnement, a ete concue a partir d'une vingtaine de principes directeurs et d'un modele d'action. Ces principes directeurs et le modele d'action decoulent de considerations theoriques psychologiques, didactiques et technologiques. La recherche decrit la structure des differentes parties composant le simulateur. L'architecture de celui-ci est construite autour d'une unite centrale, la "Principale", dont les liens et les ramifications avec les autres unites confere a l'ensemble du simulateur sa souplesse et sa

  8. Detection of elastic modes in a solid-liquid-solid planar waveguide

    NASA Astrophysics Data System (ADS)

    Ham-Rodriguez, C. I.; Manzanares-Martinez, J.; Moctezuma-Enriquez, D.; Manzanares-Martinez, B.

    2016-08-01

    In this work, we demonstrate that acoustic ultra-short pulses can be used to characterize multiple guided modes in a solid-liquid-solid planar waveguide via the determination of the time of flight (τ) using the Short Time Fourier Transform (STFT). To obtain experimentally τ, we introduce a time dependent ultra-short acoustic signal s(t) at one side of a finite waveguide and we perform the STFT of the outgoing acoustic signal s'(t) from the other side. We have found that this technique is able to discriminate the signature of multiple even and odd modes at the same experimental run.

  9. On the solute coupling at the moving solid/liquid interface during equiaxed solidification

    NASA Astrophysics Data System (ADS)

    Yao, X.

    2006-08-01

    Integral mass conservation was widely accepted for the solute coupling to solve solute redistribution during equiaxed solidification so far. The present study revealed that the integral form was invalid for moving boundary problems as it could not represent the mass balance at the moving interface. Accordingly, differential mass conservation at the solid/liquid interface was used to solve solute diffusion for spherical geometry. The model was applied for hydrogen diffusion in solidification to validate that the hydrogen enrichment was significant and depended on the growth rate.

  10. The Discrete Multi-Hybrid System for the Simulation of Solid-Liquid Flows

    PubMed Central

    Alexiadis, Alessio

    2015-01-01

    This study proposes a model based on the combination of Smoothed Particle Hydrodynamics, Coarse Grained Molecular Dynamics and the Discrete Element Method for the simulation of dispersed solid-liquid flows. The model can deal with a large variety of particle types (non-spherical, elastic, breakable, melting, solidifying, swelling), flow conditions (confined, free-surface, microscopic), and scales (from microns to meters). Various examples, ranging from biological fluids to lava flows, are simulated and discussed. In all cases, the model captures the most important features of the flow. PMID:25961561

  11. Determination of the mean solid-liquid interface energy of pivalic acid

    NASA Technical Reports Server (NTRS)

    Singh, N. B.; Gliksman, M. E.

    1989-01-01

    A high-confidence solid-liquid interfacial energy is determined for an anisotropic material. A coaxial composite having a cylindrical specimen chamber geometry provides a thermal gradient with an axial heating wire. The surface energy is derived from measurements of grain boundary groove shapes. Applying this method to pivalic acid, a surface energy of 2.84 erg/sq cm was determined with a total systematic and random error less than 10 percent. The value of interfacial energy corresponds to 24 percent of the latent heat of fusion per molecule.

  12. Distribution of solute at solid-liquid interface during solidification of melt

    NASA Astrophysics Data System (ADS)

    Fukui, Keisuke; Maeda, Kouji

    1998-11-01

    A model for predicting a distribution coefficient (ki) of solute at the solid-liquid (S-L) interface, when the solid layer is growing, is proposed. The interfacial distribution coefficient is expressed as a function of two gradients of the liquid concentration and equilibrium concentration at the S-L interface. The model is applied to the solidification of a simple eutectic binary liquid of lauric acid and myristic acid in an enclosed rectangular box in which a vertical wall is cooled. The impurity-concentration profile in solid is predicted from the direct numerical computations.

  13. Synthesis of gold-silica composite nanowires through solid-liquid-solid phase growth.

    PubMed

    Paulose, Maggie; Varghese, Oomman K; Grimes, Craig A

    2003-08-01

    Nanoscale wires of silicon oxide, and silicon oxide with embedded gold-silicide nanospheres, are synthesized by heating of a gold-coated silicon wafer at temperatures of 1000 degrees C or above, with the resulting wires having diameters ranging from 30 to 150 nm and lengths of approximately 1 mm. This simple fabrication process should make possible economical bulk production of nanowires. Studies indicate that the growth of these gold-silica composite nanowires occurs directly on the silicon wafer by a solid-liquid-solid mechanism. PMID:14598450

  14. Surface-induced selection during in situ photoswitching at the solid/liquid interface.

    PubMed

    Bonacchi, Sara; El Garah, Mohamed; Ciesielski, Artur; Herder, Martin; Conti, Simone; Cecchini, Marco; Hecht, Stefan; Samorì, Paolo

    2015-04-13

    Here we report for the first time a submolecularly resolved scanning tunneling microscopy (STM) study at the solid/liquid interface of the in situ reversible interconversion between two isomers of a diarylethene photoswitch, that is, open and closed form, self-assembled on a graphite surface. Prolonged irradiation with UV light led to the in situ irreversible formation of another isomer as by-product of the reaction, which due to its preferential physisorption accumulates at the surface. By making use of a simple yet powerful thermodynamic model we provide a quantitative description for the observed surface-induced selection of one isomeric form. PMID:25728405

  15. Investigating the solid-liquid phase transition of water nanofilms using the generalized replica exchange method

    SciTech Connect

    Lu, Qing; Kim, Jaegil; Straub, John E.; Farrell, James D.; Wales, David J.

    2014-11-14

    The generalized Replica Exchange Method (gREM) was applied to study a solid-liquid phase transition in a nanoconfined bilayer water system using the monatomic water (mW) model. Exploiting optimally designed non-Boltzmann sampling weights with replica exchanges, gREM enables an effective sampling of configurations that are metastable or unstable in the canonical ensemble via successive unimodal energy distributions across phase transition regions, often characterized by S-loop or backbending in the statistical temperature. Extensive gREM simulations combined with Statistical Temperature Weighted Histogram Analysis Method (ST-WHAM) for nanoconfined mW water at various densities provide a comprehensive characterization of diverse thermodynamic and structural properties intrinsic to phase transitions. Graph representation of minimized structures of bilayer water systems determined by the basin-hopping global optimization revealed heterogeneous ice structures composed of pentagons, hexagons, and heptagons, consistent with an increasingly ordered solid phase with decreasing density. Apparent crossover from a first-order solid-liquid transition to a continuous one in nanoconfined mW water with increasing density of the system was observed in terms of a diminishing S-loop in the statistical temperature, smooth variation of internal energies and heat capacities, and a characteristic variation of lateral radial distribution functions, and transverse density profiles across transition regions.

  16. A level set method for solid-liquid interface tracking in texturally equilibrated pore networks

    NASA Astrophysics Data System (ADS)

    Ghanbarzadeh, Soheil; Hesse, Marc; Prodanovic, Masa

    2015-04-01

    The properties of some porous media are determined by their evolution towards textural equilibrium. Melt drainage from temperate glacier ice and the accumulation of hydrocarbons beneath rock salt are two examples in natural systems. In these materials, pore geometry evolves to minimize the solid-liquid interfacial energy while maintaining dihedral angle, θ, at solid-liquid contact lines. In this work we present the first computations of 3-D texturally equilibrated pore networks using a novel level set method. Interfacial energy minimization is achieved by evolving interface under surface diffusion to constant mean curvature surface. The porosity and dihedral angle constraints are added to the formulation using virtual velocity terms. A domain decomposition scheme is devised to restrict the computational domain and the coupling between the interfaces is achieved on the original computational domain. For the last 30 years, explicit representation of the interfaces limited the computations to highly idealized geometries. The presented model overcomes these limitations and opens the door to the exploration of the physics of these materials in realistic systems. For example, our results show that the fully wetted grain boundaries exist even for θ>0 which reconciles the theory with experimental observations. This work is sponsored by the Statoil Fellows Program at The University of Texas.

  17. Monitoring the solid-liquid interface in tanks using profiling sonar and 3D visualization techniques

    NASA Astrophysics Data System (ADS)

    Sood, Nitin; Zhang, Jinsong; Roelant, David; Srivastava, Rajiv

    2005-03-01

    Visualization of the interface between settled solids and the optically opaque liquid above is necessary to facilitate efficient retrieval of the high-level radioactive waste (HLW) from underground storage tanks. A profiling sonar was used to generate 2-D slices across the settled solids at the bottom of the tank. By incrementally rotating the sonar about its centerline, slices of the solid-liquid interface can be imaged and a 3-D image of the settled solids interface generated. To demonstrate the efficacy of the sonar in real-time solid-liquid interface monitoring systems inside HLW tanks, two sets of experiments were performed. First, various solid objects and kaolin clay (10 μm dia) were successfully imaged while agitating with 30% solids (by weight) entrained in the liquid. Second, a solid with a density similar to that of the immersed fluid density was successfully imaged. Two dimensional (2-D) sonar images and the accuracy and limitations of the in-tank imaging will be presented for these two experiments. In addition, a brief review of how to utilize a 2-D sonar image to generate a 3-D surface of the settled layer within a tank will be discussed.

  18. Pressure cell for investigations of solid-liquid interfaces by neutron reflectivity

    NASA Astrophysics Data System (ADS)

    Kreuzer, Martin; Kaltofen, Thomas; Steitz, Roland; Zehnder, Beat H.; Dahint, Reiner

    2011-02-01

    We describe an apparatus for measuring scattering length density and structure of molecular layers at planar solid-liquid interfaces under high hydrostatic pressure conditions. The device is designed for in situ characterizations utilizing neutron reflectometry in the pressure range 0.1-100 MPa at temperatures between 5 and 60 °C. The pressure cell is constructed such that stratified molecular layers on crystalline substrates of silicon, quartz, or sapphire with a surface area of 28 cm2 can be investigated against noncorrosive liquid phases. The large substrate surface area enables reflectivity to be measured down to 10-5 (without background correction) and thus facilitates determination of the scattering length density profile across the interface as a function of applied load. Our current interest is on the stability of oligolamellar lipid coatings on silicon surfaces against aqueous phases as a function of applied hydrostatic pressure and temperature but the device can also be employed to probe the structure of any other solid-liquid interface.

  19. Pressure cell for investigations of solid-liquid interfaces by neutron reflectivity.

    PubMed

    Kreuzer, Martin; Kaltofen, Thomas; Steitz, Roland; Zehnder, Beat H; Dahint, Reiner

    2011-02-01

    We describe an apparatus for measuring scattering length density and structure of molecular layers at planar solid-liquid interfaces under high hydrostatic pressure conditions. The device is designed for in situ characterizations utilizing neutron reflectometry in the pressure range 0.1-100 MPa at temperatures between 5 and 60 °C. The pressure cell is constructed such that stratified molecular layers on crystalline substrates of silicon, quartz, or sapphire with a surface area of 28 cm(2) can be investigated against noncorrosive liquid phases. The large substrate surface area enables reflectivity to be measured down to 10(-5) (without background correction) and thus facilitates determination of the scattering length density profile across the interface as a function of applied load. Our current interest is on the stability of oligolamellar lipid coatings on silicon surfaces against aqueous phases as a function of applied hydrostatic pressure and temperature but the device can also be employed to probe the structure of any other solid-liquid interface. PMID:21361606

  20. Convective influence on the stability of a cylindrical solid-liquid interface

    NASA Technical Reports Server (NTRS)

    Fang, Q. T.; Glicksman, M. E.; Coriell, S. R.; Mcfadden, G. B.; Boisvert, R. F.

    1985-01-01

    Experiments in which a long vertical, heated wire is surrounded by concentric annuli of a melt and its crystalline solid show that the convection state changes from a stable unicell surrounded by a stationary cylindrical solid-liquid interface, to a complex time-dependent flow surrounded by a rotating, helical solid-liquid interface. This transition occurs at a Grashof number of approximately 150, which is an order of magnitude less than the critical Grashof number calculated for a liquid annulus surrounded by rigid walls. A linear stability analysis has been carried out for an infinitely tall vertical annulus. When the deformable nature of the crystal-melt interface is taken into account in the boundary conditions, two new modes of instability arise. The most dangerous mode is asymmetrical and corresponds to helical waves travelling vertically upwards. The critical Grashof number and the scaling properties of the eigenstate agree with experiments. The results clearly demonstrate the coupling of convection with crystal-melt interfacial instabilities.

  1. Modified phase-field-crystal model for solid-liquid phase transitions

    NASA Astrophysics Data System (ADS)

    Guo, Can; Wang, Jincheng; Wang, Zhijun; Li, Junjie; Guo, Yaolin; Tang, Sai

    2015-07-01

    A modified phase-field-crystal (PFC) model is proposed to describe solid-liquid phase transitions by reconstructing the correlation function. The effects of fitting parameters of our modified PFC model on the bcc-liquid phase diagram, numerical stability, and solid-liquid interface properties during planar interface growth are examined carefully. The results indicate that the increase of the correlation function peak width at k =km will enhance the stability of the ordered phase, while the increase of peak height at k =0 will narrow the two-phase coexistence region. The third-order term in the free-energy function and the short wave-length of the correlation function have significant influences on the numerical stability of the PFC model. During planar interface growth, the increase of peak width at k =km will decrease the interface width and the velocity coefficient C , but increase the anisotropy of C and the interface free energy. Finally, the feasibility of the modified phase-field-crystal model is demonstrated with a numerical example of three-dimensional dendritic growth of a body-centered-cubic structure.

  2. Modified phase-field-crystal model for solid-liquid phase transitions.

    PubMed

    Guo, Can; Wang, Jincheng; Wang, Zhijun; Li, Junjie; Guo, Yaolin; Tang, Sai

    2015-07-01

    A modified phase-field-crystal (PFC) model is proposed to describe solid-liquid phase transitions by reconstructing the correlation function. The effects of fitting parameters of our modified PFC model on the bcc-liquid phase diagram, numerical stability, and solid-liquid interface properties during planar interface growth are examined carefully. The results indicate that the increase of the correlation function peak width at k=k(m) will enhance the stability of the ordered phase, while the increase of peak height at k=0 will narrow the two-phase coexistence region. The third-order term in the free-energy function and the short wave-length of the correlation function have significant influences on the numerical stability of the PFC model. During planar interface growth, the increase of peak width at k=k(m) will decrease the interface width and the velocity coefficient C, but increase the anisotropy of C and the interface free energy. Finally, the feasibility of the modified phase-field-crystal model is demonstrated with a numerical example of three-dimensional dendritic growth of a body-centered-cubic structure. PMID:26274309

  3. Evaluation and ranking of the tank focus area solid liquid separation needs

    SciTech Connect

    McCabe, D.J.

    1995-08-17

    The Tank Focus Area (TFA) of the Department of Energy (DOE) Office of Environmental Restoration and Waste Management (EM) addresses remediation of liquid waste currently stored in underground tanks. Several baseline technologies for treatment of tank waste can be categorized into three types of solid liquid separation: (a) removal of radioactive species that have been absorbed or precipitated, (b) pretreatment for ion exchange, and (c) volume reduction of sludge and wash water. The solids formed from precipitation or absorption of radioactive ions require separation from the liquid phase to permit treatment of the liquid as Low Level Waste. Prior to ion exchange of radioactive ions, removal of insoluble solids is needed to prevent bed fouling and downstream contamination. Volume reduction of washed sludge solids would reduce the tank space required for interim storage. The scope of this document is to evaluate the solid/liquid separations needed to permit treatment of tank wastes to accomplish these goals. The document summarizes previous alkaline waste testing, with an emphasis on crossflow filtration, to-obtain a general understanding of the behavior of radioactive wastes on available equipment. The document also provides general information about filtration and a path forward for testing.

  4. Kerr-AdS analogue of triple point and solid/liquid/gas phase transition

    NASA Astrophysics Data System (ADS)

    Altamirano, Natacha; Kubizňák, David; Mann, Robert B.; Sherkatghanad, Zeinab

    2014-02-01

    We study the thermodynamic behavior of multi-spinning d = 6 Kerr-anti de Sitter black holes in the canonical ensemble of fixed angular momenta J1 and J2. We find, dependent on the ratio q = J2/J1, qualitatively different interesting phenomena known from the ‘every day thermodynamics’ of simple substances. For q = 0 the system exhibits recently observed reentrant large/small/large black hole phase transitions, but for 0 < q ≪ 1 we find an analogue of a ‘solid/liquid’ phase transition. Furthermore, for q ∈ (0.00905, 0.0985) the system displays the presence of a large/intermediate/small black hole phase transition with two critical and one triple (or tricritical) points. This behavior is reminiscent of the solid/liquid/gas phase transition except that the coexistence line of small and intermediate black holes does not continue for an arbitrary value of pressure (similar to the solid/liquid coexistence line) but rather terminates at one of the critical points. Finally, for q > 0.0985 we observe the ‘standard liquid/gas behavior’ of the Van der Waals fluid.

  5. A New Paradigm of Computer Graphics by Universal Solver for Solid, Liquid and Gas

    NASA Astrophysics Data System (ADS)

    Yabe, Takashi; Takizawa, Kenji; Xiao, Feng; Aoki, Takayuki; Himeno, Takehiro; Takahashi, Tsunemi; Kunimatsu, Atsushi

    We propose a new algorithm for producing computer graphics of melting and evaporation process of matter. Such a computation becomes possible by a universal solver for solid, liquid and gas based on the CIP (Cubic-Interpolated Propagation / Constrained Interpolation Profile) method proposed by one of the authors. This method can also be applied to the movement, deformation and even break up of solid, liquid and gas in one simple algorithm. Therefore seamless computation of all the phases of matter becomes possible. This enables us to reproduce natural phenomena in some instances by computation. In order to demonstrate this reality, we show how precisely the computational result replicates the movies of real phenomena. The flattering motions of metal disk in water and thin name card in air are treated showing accuracy of force calculation on the surface of sub-grid scale. Although the CIP uses semi-Lagrangian form algorithm, the exact mass conservation is guaranteed by additional tool. By using this scheme, separation of a bubble in bifurcation tube and splashing of water surface are successfully simulated.

  6. Digital microfluidics platform for interfacing solid-liquid extraction column with portable capillary electropherograph for analysis of soil amino acids.

    PubMed

    Gorbatsova, Jelena; Jaanus, Martin; Vaher, Merike; Kaljurand, Mihkel

    2016-02-01

    In this work, the concept of a field-portable analyzer is proposed that operates with milliliter amounts of solvents and samples. The need to develop such an analyzer is not only driven by specific extraterrestrial analysis but also, for example, by forensics applications where the amount of liquid that can be taken to the field is severely limited. The prototype of the proposed analyzer consists of a solid-liquid extractor, the output of which is connected to the micropump, which delivers droplets of extracts to digital microfluidic platform (DMFP). In this way, world-to-chip interfacing is established. Further, the sample droplets are transported to CE capillary inlet port, separated and detected via a contactless conductivity detector. Working buffers and other solvents needed to perform CE analysis are also delivered as droplets to the DMFP and transported through the CE capillary. The performance of the analyzer is demonstrated by analysis of amino acids in sand matrices. The recovery of the spiked amino acids from the inert sand sample was from 34 to 51% with analysis LOD from 0.2 to 0.6 ppm and migration time RSD from 0.2 to 6.0%. PMID:26426309

  7. Experimental study of the solid-liquid interface in a yield-stress fluid flow upstream of a step

    NASA Astrophysics Data System (ADS)

    Luu, Li-Hua; Pierre, Philippe; Guillaume, Chambon

    2014-11-01

    We present an experimental study where a yield-stress fluid is implemented to carefully examine the interface between a liquid-like unyielded region and a solid-like yielded region. The studied hydrodynamics consists of a rectangular pipe-flow disturbed by the presence of a step. Upstream of the step, a solid-liquid interface between a dead zone and a flow zone appears. This configuration can both model geophysical erosion phenomenon in debris flows or find applications for industrial extrusion processes. We aim to investigate the dominant physical mechanism underlying the formation of the static domain, by combining the rheological characterization of the yield-stress fluid with local measurements of the related hydrodynamic parameters. In this work, we use a model fluid, namely polymer micro-gel Carbopol, that exhibits a Hershel-Bulkley viscoplastic rheology. Exploiting the fluid transparency, the flow is monitored by Particle Image Velocimetry thanks to internal visualization technique. In particular, we demonstrate that the flow above the dead zone roughly behaves as a plug flow whose velocity profile can successfully be described by a Poiseuille equation including a Hershel-Bulkley rheology (PHB theory), with exception of a thin zone at the close vicinity of the static domain. The border inside the flow zone above which the so-called PHB flow starts, is found to be the same regardless of the flow rate and to move with a constant velocity that increases with the flow rate. We interpret this feature as a slip frontier.

  8. Accommodative Behavior of Non-porous Molecular crystal at Solid-Gas and Solid-Liquid Interface

    PubMed Central

    Mande, Hemant M.; Ghalsasi, Prasanna S.

    2015-01-01

    Molecular crystals demonstrate drastically different behavior in solid and liquid state, mainly due to their difference in structural frameworks. Therefore, designing of unique structured molecular compound which can work at both these interfaces has been a challenge. Here, we present remarkable ‘molecular’ property by non-porous molecular solid crystal, dinuclear copper complex (C6H5CH(X)NH2)2CuCl2, to reversibly ‘adsorb’ HCl gas at solid-gas interface as well as ‘accommodate’ azide anion at solid-liquid interface with crystal to crystal transformation. The latter process is driven by molecular recognition, self-assembly, and anchimeric assistance. The observed transformations are feasible due to breathing of inner and outer coordination sphere around metal center resulting in change in metal polyhedra for ‘accommodating’ guest molecule. These transformations cause changes in optical, magnetic, and/or ferroelectric property offering diversity in ‘sensing’ application. With the proposed underlying principles in these exceptional reversible and cyclic transformations, we prepared a series of compounds, can facilitate designing of novel multifunctional molecular materials. PMID:26411980

  9. A Simple Approach to Characterize Gas-Aqueous Liquid Two-phase Flow Configuration Based on Discrete Solid-Liquid Contact Electrification

    PubMed Central

    Choi, Dongwhi; Lee, Donghyeon; Sung Kim, Dong

    2015-01-01

    In this study, we first suggest a simple approach to characterize configuration of gas-aqueous liquid two–phase flow based on discrete solid-liquid contact electrification, which is a newly defined concept as a sequential process of solid-liquid contact and successive detachment of the contact liquid from the solid surface. This approach exhibits several advantages such as simple operation, precise measurement, and cost-effectiveness. By using electric potential that is spontaneously generated by discrete solid–liquid contact electrification, the configurations of the gas-aqueous liquid two-phase flow such as size of a gas slug and flow rate are precisely characterized. According to the experimental and numerical analyses on parameters that affect electric potential, gas slugs have been verified to behave similarly to point electric charges when the measuring point of the electric potential is far enough from the gas slug. In addition, the configuration of the gas-aqueous liquid two-phase microfluidic system with multiple gas slugs is also characterized by using the presented approach. For a proof-of-concept demonstration of using the proposed approach in a self-triggered sensor, a gas slug detector with a counter system is developed to show its practicality and applicability. PMID:26462437

  10. Comparison of the different responses of surface plasmon resonance and quartz crystal microbalance techniques at solid-liquid interfaces under various experimental conditions.

    PubMed

    Fang, Jiajie; Ren, Chunlai; Zhu, Tao; Wang, Kaiyu; Jiang, Zhongying; Ma, Yuqiang

    2015-02-21

    A molecular level understanding of the phenomena taking place at solid-liquid interfaces, ranging from changes in mass to conformation changes, is the key to developing and improving many chemical and biological systems and their scientific and medical applications. Surface plasmon resonance (SPR) and quartz crystal microbalance (QCM) techniques are often coupled to achieve this understanding. We divided various experimentally relevant scenarios into the following six categories: boundary solutions; surface modifications; conformation; viscoelastic properties; molecular ruler; and mass sensitivity. For each case, based on theoretical analyses, we discuss the following four points with respect to discrete adsorbates at solid-liquid interfaces: (1) the different types of information that can be obtained, why it can be obtained and how to obtain it; (2) the origins of many current approaches and why they are imperfect; (3) guidelines for experimental design; and (4) possible studies, such as the effect of dimensional confinement and adsorption forces on the ability of conformational changes to occur on the receipt of external stimuli and the hysteresis in these changes. PMID:25575354

  11. Double multiple-relaxation-time lattice Boltzmann model for solid-liquid phase change with natural convection in porous media

    NASA Astrophysics Data System (ADS)

    Liu, Qing; He, Ya-Ling

    2015-11-01

    In this paper, a double multiple-relaxation-time lattice Boltzmann model is developed for simulating transient solid-liquid phase change problems in porous media at the representative elementary volume scale. The model uses two different multiple-relaxation-time lattice Boltzmann equations, one for the flow field and the other for the temperature field with nonlinear latent heat source term. The model is based on the generalized non-Darcy formulation, and the solid-liquid interface is traced through the liquid fraction which is determined by the enthalpy-based method. The present model is validated by numerical simulations of conduction melting in a semi-infinite space, solidification in a semi-infinite corner, and convection melting in a square cavity filled with porous media. The numerical results demonstrate the efficiency and accuracy of the present model for simulating transient solid-liquid phase change problems in porous media.

  12. Coarsening in Solid-Liquid Mixtures Studied on the Space Shuttle

    NASA Technical Reports Server (NTRS)

    Caruso, John J.

    1999-01-01

    Ostwald ripening, or coarsening, is a process in which large particles in a two-phase mixture grow at the expense of small particles. It is a ubiquitous natural phenomena occurring in the late stages of virtually all phase separation processes. In addition, a large number of commercially important alloys undergo coarsening because they are composed of particles embedded in a matrix. Many of them, such as high-temperature superalloys used for turbine blade materials and low-temperature aluminum alloys, coarsen in the solid state. In addition, many alloys, such as the tungsten-heavy metal systems, coarsen in the solid-liquid state during liquid phase sintering. Numerous theories have been proposed that predict the rate at which the coarsening process occurs and the shape of the particle size distribution. Unfortunately, these theories have never been tested using a system that satisfies all the assumptions of the theory. In an effort to test these theories, NASA studied the coarsening process in a solid-liquid mixture composed of solid tin particles in a liquid lead-tin matrix. On Earth, the solid tin particles float to the surface of the sample, like ice in water. In contrast, in a microgravity environment this does not occur. The microstructures in the ground- and space-processed samples (see the photos) show clearly the effects of gravity on the coarsening process. The STS-83-processed sample (right image) shows nearly spherical uniformly dispersed solid tin particles. In contrast, the identically processed, ground-based sample (left image) shows significant density-driven, nonspherical particles, and because of the higher effective solid volume fraction, a larger particle size after the same coarsening time. The "Coarsening in Solid-Liquid Mixtures" (CSLM) experiment was conducted in the Middeck Glovebox facility (MGBX) flown aboard the shuttle in the Microgravity Science Laboratory (MSL-1/1R) on STS-83/94. The primary objective of CSLM is to measure the temporal

  13. New Composite Membranes for High Throughput Solid-Liquid Separations at the Savannah River Site

    SciTech Connect

    Bhave, Ramesh R

    2012-01-01

    New Composite Membranes for High Throughput Solid-Liquid Separations at the Savannah River Site R. Bhave (Oak Ridge National Laboratory. Oak Ridge, TN) and M. R. Poirier* (Savannah River National Laboratory, Aiken SC) Solid-liquid separation is the limiting step for many waste treatment processes at the Savannah River Site. SRNL researchers have identified the rotary microfilter as a technology to improve the rate of solid-liquid separation processes. SRNL is currently developing the rotary microfilter for radioactive service and plans to deploy the technology as part of the small column ion exchange process. The rotary microfilter can utilize any filter media that is available as a flat sheet. The current baseline membrane is a 0.5 micron (nominal) porous metal filter (Pall PMM050). Previous testing with tubular filters showed that filters composed of a ceramic membrane on top of a stainless steel support produce higher flux than filters composed only of porous metal. The authors are working to develop flat sheet filter media composed of a ceramic membrane and/or ceramic-metal composite on top of a porous stainless steel support that can be used with the rotary microfilter to substantially increase filter flux resulting in a more compact, energy efficient and cost-effective high level radioactive waste treatment system. Composite membranes with precisely controlled pore size distribution were fabricated on porous metal supports. High quality uniform porous metal (316SS) supports were fabricated to achieve high water permeability. Separative layers of several different materials such as ultrafine metal particles and ceramic oxides were used to fabricate composite membranes. The fabrication process involved several high temperature heat treatments followed by characterization of gas and liquid permeability measurements and membrane integrity analysis. The fabricated composite membrane samples were evaluated in a static test cell manufactured by SpinTek. The

  14. SOLIEX: A Novel Solid-Liquid Method of Radionuclides Extraction from Radioactive Waste Solutions - 13486

    SciTech Connect

    Shilova, E.; Viel, P.; Huc, V.

    2013-07-01

    This paper describes recent developments in new solid-liquid extraction method, called SOLIEX, to remove cesium from alkaline solutions. SOLIEX relies on the use of a reversible complexing system comprising a carbon felt bearing molecular traps (calixarenes). This complexing system exhibits a high selectivity for Cs, and is thus expected to be helpful for the treatment of highly diluted cesium wastes even with a high concentration of competing alkali metal cations. As additional advantage, this complexing system can be adapted by molecular engineering to capture other radionuclides, such as Sr, Eu, Am. Finally, this complexing system can be easily and efficiently regenerated by using a cost effective stripping procedure, which limits further generation of waste to meet 'zero liquid' discharge requirements for nuclear facilities. (authors)

  15. Anaerobic digestion of acidified slurry fractions derived from different solid-liquid separation methods.

    PubMed

    Sutaryo, Sutaryo; Ward, Alastair James; Møller, Henrik Bjarne

    2013-02-01

    Batch assays investigating the ultimate methane yields (B(0)) of acidified slurry fractions produced with different solid-liquid slurry separation techniques were done. The result showed that the anaerobic digestion (AD) process was inhibited when raw and liquid fractions of sow, pig and dairy cow acidified slurry are digested, but AD treating solid fractions (SF) acidified slurry showed no sulphide inhibition. The B(0) of SF acidified sow slurry increased significantly with increasing screen size in the screw press. No significant effect of acidification processes on B(0) of SF dairy cow slurry (DCS) was observed. The ultimate methane yields of SF acidified DCS and SF non acidified DCS were 278±13 and 289±1LkgVS(-1), while in term of fresh weigh substrate were 59±2.8 and 59±0.3Lkgsubstrate(-1), respectively. PMID:23313767

  16. Local conformational switching of supramolecular networks at the solid/liquid interface.

    PubMed

    Cometto, Fernando P; Kern, Klaus; Lingenfelder, Magalí

    2015-05-26

    We use the electric field in a scanning tunneling microscope to manipulate the transition between open and close packed 2D supramolecular networks of neutral molecules in nonpolar media. We found that while the magnitude of the applied field is not decisive, it is the sign of the polarization that needs to be maintained to select one particular polymorph. Moreover, the switching is independent of the solvent used and fully reversible. We propose that the orientation of the surface dipole determined by the electric field might favor different conformation-depended charge transfer mechanisms of the adsorbates to the surface, inducing open (closed) structures for negative (positive) potentials. Our results show the use of local fields to select the polymorphic outcome of supramolecular assemblies at the solid/liquid interface. The effect has potential to locally control the capture and release of analytes in host-guest systems and the 2D morphology in multicomponent layers. PMID:25857528

  17. Influence of solid-liquid separation strategy on biogas yield from a stratified swine production system.

    PubMed

    Cestonaro do Amaral, André; Kunz, Airton; Radis Steinmetz, Ricardo Luis; Scussiato, Lucas Antunes; Tápparo, Deisi Cristina; Gaspareto, Taís Carla

    2016-03-01

    As the fourth largest swine producer and exporter, Brazil has increased its participation in the global swine production market. Generally, these units concentrate a large number of animals and generate effluents that must be correctly managed to prevent environmental impacts, being anaerobic digestion is an interesting alternative for treating these effluents. The low-volatile solid concentration in the manure suggests the need for solid-liquid separation as a tool to improve the biogas generation capacity. This study aimed to determine the influence of simplified and inexpensive solid-liquid separation strategies (screening and settling) and the different manures produced during each swine production phase (gestating and farrowing sow houses, nursery houses and finishing houses) on biogas and methane yield. We collected samples in two gestating sow houses (GSH-a and GSH-b), two farrowing sow houses (FSH-a and FSH-b), a nursery house (NH) and a finishing house (FH). Biochemical methane potential (BMP) tests were performed according to international standard procedures. The settled sludge fraction comprised 20-30% of the raw manure volume, which comprises 40-60% of the total methane yield. The methane potential of the settled sludge fraction was approximately two times higher than the methane potential of the supernatant fraction. The biogas yield differed among the raw manures from different swine production phases (GSH-a 326.4 and GSH-b 577.1; FSH-a 860.1 and FSH-b 479.2; NH -970.2; FH 474.5 NmLbiogas.gVS(-1)). The differences were relative to the production phase (feed type and feeding techniques) and the management of the effluent inside the facilities (water management). Brazilian swine production has increased his participation in the global market, been the fourth producer and the fourth exporter. The segregation of swine production in multiple sites has increased its importance, due to the possibilities to have more specialized units. Generally, these units

  18. Ginzburg-Landau theory for the solid-liquid interface of bcc elements

    NASA Technical Reports Server (NTRS)

    Shih, W. H.; Wang, Z. Q.; Zeng, X. C.; Stroud, D.

    1987-01-01

    Consideration is given to a simple order-parameter theory for the interfacial tension of body-centered-cubic solids in which the principal order parameter is the amplitude of the density wave at the smallest nonzero reciprocal-lattice vector of the solid. The parameters included in the theory are fitted to the measured heat of fusion, melting temperature, and solid-liquid density difference, and to the liquid structure factor and its temperature derivative at freezing. Good agreement is found with experiment for Na and Fe and the calculated anisotropy of the surface tension among different crystal faces is of the order of 2 percent. On the basis of various assumptions about the universal behavior of bcc crystals at melting, the formalism predicts that the surface tension is proportional to the heat of fusion per surface atom.

  19. Preparation of a smooth GaN-Gallium solid-liquid interface

    NASA Astrophysics Data System (ADS)

    de Jong, A. E. F.; Vonk, V.; Ruat, M.; Boćkowski, M.; Kamler, G.; Grzegory, I.; Honkimäki, V.; Vlieg, E.

    2016-08-01

    We discuss the preparation of an atomically flat solid-liquid interface between solid gallium nitride and liquid gallium using in situ surface X-ray diffraction to probe the interface roughness. For the creation of this interface it is necessary to start the experiment with liquid gallium which first etches into the solid at a temperature of 823 K in a nitrogen free ambient. After this rigorous cleaning procedure there is perfect wetting between solid and liquid. The roughness created due to the fast etching of the solid has to be repaired at a nitrogen pressure of 10-20 bar and a temperature around 1150 K. The (2,1) crystal truncation rod data are excellently described by a surface model having 0±0.1 Å roughness, which indicates a successful repair. The lateral length scale on which the roughness is determined has a lower limit of 750±50 Å.

  20. Modeling of ultrasound transmission through a solid-liquid interface comprising a network of gas pockets

    SciTech Connect

    Paumel, K.; Baque, F.; Moysan, J.; Corneloup, G.; Chatain, D.

    2011-08-15

    Ultrasonic inspection of sodium-cooled fast reactor requires a good acoustic coupling between the transducer and the liquid sodium. Ultrasonic transmission through a solid surface in contact with liquid sodium can be complex due to the presence of microscopic gas pockets entrapped by the surface roughness. Experiments are run using substrates with controlled roughness consisting of a network of holes and a modeling approach is then developed. In this model, a gas pocket stiffness at a partially solid-liquid interface is defined. This stiffness is then used to calculate the transmission coefficient of ultrasound at the entire interface. The gas pocket stiffness has a static, as well as an inertial component, which depends on the ultrasonic frequency and the radiative mass.

  1. Design of a monochromatic ellipsometer for studies at the solid-liquid interface

    NASA Astrophysics Data System (ADS)

    Pai-Panandiker, R. S.; Dorgan, J. R.

    1995-02-01

    A new design for a monochromatic ellipsometer used for studies at the solid-liquid interface is described. The design of the ellipsometer incorporates two novel features—a special optical glass cell and a thermally controlled sample oven. The ellipsometer design allows for in situ kinetic studies through use of the optical glass cell. Furthermore, the apparatus is modified to allow thermal equilibration over a range of temperatures. The temperature response of the cell assembly is presented and the response time is seen to be approximately 1 h. Data on the adsorption of a diblock copolymer [poly(ethylene oxide)-block-polystyrene] are presented; the analyzed data agree with previous studies on the same system.

  2. Numerical Calculation of the Morphology of a Solid/Liquid Interface Near an Insoluble Particle

    NASA Technical Reports Server (NTRS)

    Catalina, Adrian V.; Stefanescu, Doru M.; Sen, Subhayu

    2003-01-01

    A numerical mathematical model capable of accurately describing the evolution of the shape of the solid/liquid interface in the proximity of a foreign particle is presented in this paper. The model accounts for the influence of the temperature gradient and the Gibbs-Thomson and disjoining pressure effects. It shows that for the systems characterized by k(sub P) < k(sub L) the disjoining pressure causes the interface curvature to change its sign in the close-contact particle/interface region. It also shows that the increase of the temperature gradient diminishes the effect of the disjoining pressure. Calculated critical solidification velocities for the pushing/engulfment transition are compared with experimental measurements performed in microgravity conditions.

  3. Measurement of solid liquid interfacial energy in the pyrene succinonitrile monotectic system

    NASA Astrophysics Data System (ADS)

    Akbulut, S.; Ocak, Y.; Böyük, U.; Erol, M.; Keslioglu, K.; Marasli, N.

    2006-09-01

    The equilibrated grain boundary groove shapes for solid pyrene (PY) in equilibrium with the PY succinonitrile (SCN) monotectic liquid were directly observed. From the observed grain boundary groove shapes, the Gibbs-Thomson coefficient and solid-liquid interfacial energy for solid PY in equilibrium with the PY SCN monotectic liquid have been determined to be (8.72 ± 0.87) × 10-8 K m and (21.9 ± 3.28) × 10-3 J m-2 with the present numerical method and Gibbs-Thomson equation, respectively. The grain boundary energy of the solid PY phase has been determined to be (42.84 ± 7.28) × 10-3 J m-2 from the observed grain boundary groove shapes. Thermal conductivities of solid and liquid phases for PY-2.5 mol% SCN alloy and pure PY have also been measured.

  4. New density functional approach for solid-liquid-vapor transitions in pure materials.

    PubMed

    Kocher, Gabriel; Provatas, Nikolas

    2015-04-17

    A new phase field crystal (PFC) type theory is presented, which accounts for the full spectrum of solid-liquid-vapor phase transitions within the framework of a single density order parameter. Its equilibrium properties show the most quantitative features to date in PFC modeling of pure substances, and full consistency with thermodynamics in pressure-volume-temperature space is demonstrated. A method to control either the volume or the pressure of the system is also introduced. Nonequilibrium simulations show that 2- and 3-phase growth of solid, vapor, and liquid can be achieved, while our formalism also allows for a full range of pressure-induced transformations. This model opens up a new window for the study of pressure driven interactions of condensed phases with vapor, an experimentally relevant paradigm previously missing from phase field crystal theories. PMID:25933321

  5. Effects of Solid-Liquid Mixing on Microstructure of Semi-Solid A356 Aluminum Alloy

    NASA Astrophysics Data System (ADS)

    Guo, H. M.; Wang, L. J.; Wang, Q.; Yang, X. J.

    2014-08-01

    The desired starting material for semi-solid processing is the semi-solid slurry in which the solid phase is present as fine and globular particles. A modified solid-liquid mixing (SLM) is reported wherein semi-solid slurry can be produced by mixing a solid alloy block into a liquid alloy, and mechanical vibration is utilized to enhance the mixing. Effects such as liquid alloy temperature, mass ratio, and mixing intensity on the microstructure and the cooling curves during SLM were evaluated. 2D and 3D microstructure analysis of treated A356 aluminum alloy shows that microstructure can be refined significantly with a considerable morphology change in primary Al phase. It is critical that the temperature of mixture after mixing is lower than its liquidus temperature to obtain a valid SLM process. Specially, mixing intensity is identified as a primary factor for a favorable microstructure of semi-solid slurry.

  6. Surface Specularity as an Indicator of Shock-induced Solid-liquid Phase Transitions in Tin

    SciTech Connect

    G. D. Stevens, S. S. Lutz, B. R. Marshall, W.D. Turley, et al.

    2007-12-01

    When highly polished metal surfaces melt upon release after shock loading, they exhibit features that suggest significant surface changes accompany the phase transition. The reflection of light from such surfaces changes from specular (pre-shock) to diffuse upon melting. Typical of this phenomenon is the loss of signal light in velocity interferometer system for any reflector (VISAR) measurements, which usually occurs at pressures high enough to melt the free surface. Unlike many other potential material phase-sensitive diagnostics (e.g., reflectometry, conductivity), that show relatively small (1%-10%) changes, the specularity of reflection provides a more sensitive and definitive (>10x) indication of the solid-liquid phase transition. Data will be presented that support the hypothesis that specularity changes indicate melt in a way that can be measured easily and unambiguously.

  7. New Density Functional Approach for Solid-Liquid-Vapor Transitions in Pure Materials

    NASA Astrophysics Data System (ADS)

    Kocher, Gabriel; Provatas, Nikolas

    2015-04-01

    A new phase field crystal (PFC) type theory is presented, which accounts for the full spectrum of solid-liquid-vapor phase transitions within the framework of a single density order parameter. Its equilibrium properties show the most quantitative features to date in PFC modeling of pure substances, and full consistency with thermodynamics in pressure-volume-temperature space is demonstrated. A method to control either the volume or the pressure of the system is also introduced. Nonequilibrium simulations show that 2- and 3-phase growth of solid, vapor, and liquid can be achieved, while our formalism also allows for a full range of pressure-induced transformations. This model opens up a new window for the study of pressure driven interactions of condensed phases with vapor, an experimentally relevant paradigm previously missing from phase field crystal theories.

  8. Modeling of ultrasound transmission through a solid-liquid interface comprising a network of gas pockets

    NASA Astrophysics Data System (ADS)

    Paumel, K.; Moysan, J.; Chatain, D.; Corneloup, G.; Baqué, F.

    2011-08-01

    Ultrasonic inspection of sodium-cooled fast reactor requires a good acoustic coupling between the transducer and the liquid sodium. Ultrasonic transmission through a solid surface in contact with liquid sodium can be complex due to the presence of microscopic gas pockets entrapped by the surface roughness. Experiments are run using substrates with controlled roughness consisting of a network of holes and a modeling approach is then developed. In this model, a gas pocket stiffness at a partially solid-liquid interface is defined. This stiffness is then used to calculate the transmission coefficient of ultrasound at the entire interface. The gas pocket stiffness has a static, as well as an inertial component, which depends on the ultrasonic frequency and the radiative mass.

  9. Solid/liquid phase diagram of the ammonium sulfate/succinic acid/water system.

    PubMed

    Pearson, Christian S; Beyer, Keith D

    2015-05-14

    We have studied the low-temperature phase diagram and water activities of the ammonium sulfate/succinic acid/water system using differential scanning calorimetry and infrared spectroscopy of thin films. Using the results from our experiments, we have mapped the solid/liquid ternary phase diagram, determined the water activities based on the freezing point depression, and determined the ice/succinic acid phase boundary as well as the ternary eutectic composition and temperature. We also compared our results to the predictions of the extended AIM aerosol thermodynamics model (E-AIM) and found good agreement for the ice melting points in the ice primary phase field of this system; however, differences were found with respect to succinic acid solubility temperatures. We also compared the results of this study with those of previous studies that we have published on ammonium sulfate/dicarboxylic acid/water systems. PMID:25431860

  10. Force response of actively deformed polymer microdroplets: dependence on the solid/liquid boundary condition

    NASA Astrophysics Data System (ADS)

    Heppe, Jonas; McGraw, Joshua D.; Bennewitz, Roland; Jacobs, Karin

    2015-03-01

    In fluid dynamics, the solid/liquid boundary condition can play a major role in the flow behavior of a liquid. For example, in the dewetting of identical polymer films on weak slip or strong slip substrates, large qualitative and quantitative differences are observed. Therefore, when applying an external load to a liquid resting on such substrates, the measured reaction forces and the ensuing flow should also depend on the boundary condition. We present atomic force microscopy measurements in which the reaction force of a cantilever is measured as the tip pierces liquid polymer micron sized droplets and films. These indentations are done on substrates with tuned slip. Accessing the size, depth and rate dependence of the resulting force distance curves, we show an influence of the slip condition on the dissipated energy and adhesion.

  11. First-principles molecular dynamics simulations at solid-liquid interfaces with a continuum solvent.

    PubMed

    Sánchez, Verónica M; Sued, Mariela; Scherlis, Damián A

    2009-11-01

    Continuum solvent models have become a standard technique in the context of electronic structure calculations, yet no implementations have been reported capable to perform molecular dynamics at solid-liquid interfaces. We propose here such a continuum approach in a density functional theory framework using plane-wave basis sets and periodic boundary conditions. Our work stems from a recent model designed for Car-Parrinello simulations of quantum solutes in a dielectric medium [D. A. Scherlis et al., J. Chem. Phys. 124, 074103 (2006)], for which the permittivity of the solvent is defined as a function of the electronic density of the solute. This strategy turns out to be inadequate for systems extended in two dimensions: the dependence of the dielectric function on the electronic density introduces a new term in the Kohn-Sham potential, which becomes unphysically large at the interfacial region, seriously affecting the convergence of the self-consistent calculations. If the dielectric medium is properly redefined as a function of the atomic coordinates, a good convergence is obtained and the constant of motion is conserved during the molecular dynamics simulations. The Poisson problem is solved using a multigrid method, and in this way Car-Parrinello molecular dynamics simulations of solid-liquid interfaces can be performed at a very moderate computational cost. This scheme is employed to investigate the acid-base equilibrium at the TiO(2)-water interface. The aqueous behavior of titania surfaces has stimulated a large amount of experimental research, but many open questions remain concerning the molecular mechanisms determining the chemistry of the interface. Here we make an attempt to answer some of them, putting to the test our continuum model. PMID:19894999

  12. Adsorption/aggregation of surfactants and their mixtures at solid-liquid interfaces.

    PubMed

    Somasundaran, P; Huang, L

    2000-12-11

    Adsorption of surfactants and polymers at solid-liquid interfaces is used widely to modify interfacial properties in a variety of industrial processes such as flotation, ceramic processing, flocculation/dispersion, personal care product formulation and enhanced oil recovery. The behavior of surfactants and polymers at interfaces is determined by a number of forces, including electrostatic attraction, covalent bonding, hydrogen bonding, hydrophobic bonding, and solvation and desolvation of various species. The extent and type of the forces involved varies depending on the adsorbate and the adsorbent, and also the composition and other characteristics of the solvent and dissolved components in it. The influence of such forces on the adsorption behavior is reviewed here from a thermodynamics point of view. The experimental results from microcalorimetric and spectroscopic studies of adsorbed layers of different surfactant and polymer systems at solid-liquid interfaces are also presented. Calorimetric data from the adsorption of an anionic surfactant, sodium octylbenzenesulfonate, and a non-ionic surfactant, dodecyloxyheptaethoxyethylalcohol, and their mixtures on alumina, yielded important thermodynamic information. It was found that the adsorption of anionic surfactants alone on alumina was initially highly exothermic due to the electrostatic interaction with the substrate. Further adsorption leading to a solloid (hemimicelle) formation is proposed to be mainly an entropy-driven process. The entropy effect was found to be more pronounced for the adsorption of anionic-non-ionic surfactant mixtures than for the anionic surfactant alone. Fluorescence studies using a pyrene probe on an adsorbed surfactant and polymer layers, along with electron spin resonance (ESR) spectroscopy, reveal the role of surface aggregation and the conformation of the adsorbed molecules in controlling the dispersion and wettability of the system. PMID:11185696

  13. Design and Testing of a Solid-Liquid Interface Monitor for High-Level Waste Tanks

    SciTech Connect

    McDaniel, D.; Awwad, A.; Roelant, D.; Srivastava, R.

    2008-07-01

    A high-level waste (HLW) monitor has been designed, fabricated and tested at full-scale for deployment inside a Hanford tank. The Solid-Liquid Interface Monitor (SLIM) integrates a commercial sonar system with a mechanical deployment system for deploying into an underground waste tank. The system has undergone several design modifications based upon changing requirements at Hanford. We will present the various designs of the monitor from first to last and will present performance data from the various prototype systems. We will also present modeling of stresses in the enclosure under 85 mph wind loading. The system must be able to function at winds up to 15 mph and must withstand a maximum loading of 85 mph. There will be several examples presented of engineering tradeoffs made as FIU analyzed new requirements and modified the design to accommodate. We will present our current plans for installing into the Cold Test Facility at Hanford and into a double-shelled tank at Hanford. Finally, we will present our vision for how this technology can be used at Hanford and Savannah River Site to improve the filling and emptying of high-level waste tanks. In conclusion: 1. The manually operated first-generation SLIM is a viable option on tanks where personnel are allowed to work on top of the tank. 2. The remote controlled second-generation SLIM can be utilized on tanks where personnel access is limited. 3. The totally enclosed fourth-generation SLIM, when the design is finalized, can be used when the possibility exists for wind dispersion of any HLW that maybe on the system. 4. The profiling sonar can be used effectively for real-time monitoring of the solid-liquid interface over a large area. (authors)

  14. Modélisation du cycle de vie d'un polluant en atmosphère : application aux oxydes d'azote (NO{X})

    NASA Astrophysics Data System (ADS)

    Hamzi, R.; Bourmada, N.; Benamrane, B. T.; Londiche, H.

    2005-05-01

    Les problèmes de l'environnement nécessitent des modélisations particulièrement difficiles, mais d'une grande importance sociale. C'est un domaine récent, où les données sont encore peu nombreuses, mais où les attentes sont considérables, tant auprès du public que des politiques et des industriels. En effet, la modélisation consiste à définir un modèle qui permettra de représenter efficacement le processus étudié. Dans cette optique le comportement modélisé n'est que la manifestation extérieure d'une structure plus profonde. La complexité du système et du problème posé détermine celle du modèle, qui va de la simple représentation qualitative d'un comportement aux formules mathématiques les plus élaborées. Lorsque la modélisation est exprimée mathématiquement, on recourt généralement à un programme de simulation pour calculer le comportement prévisionnel du modèle. La compréhension du cycle de vie d'un polluant en atmosphère, dans notre cas les oxydes d'azote (NOX), nécessite la modélisation de l'évolution des réactifs et des produits en fonction du temps exprimée par des équations différentielles. La réalisation de la simulation à partir de ces modèles, nous permet de connaître l'ensemble des processus ayant lieu lors de l'émission du polluant en atmosphère jusqu'à sa consommation.

  15. Laboratory Production of Lemon Liqueur (Limoncello) by Conventional Maceration and a Two-Syringe System to Illustrate Rapid Solid-Liquid Dynamic Extraction

    ERIC Educational Resources Information Center

    Naviglio, Daniele; Montesano, Domenico; Gallo, Monica

    2015-01-01

    Two experimental techniques of solid-liquid extraction are compared relating to the lab-scale production of lemon liqueur, most commonly named "limoncello"; the first is the official method of maceration for the solid-liquid extraction of analytes and is widely used to extract active ingredients from a great variety of natural products;…

  16. Manifestations de la transition solide-liquide dans les agrégats

    NASA Astrophysics Data System (ADS)

    Calvo, F.

    The thermodynamics of clusters is a subject of increasing interest, both from the theoretical and experimental points of view. We present a set of theoretical and numerical methods for studying phase transitions, especially the solid-liquid transition, in atomic or molecular clusters. Several means of characterization (thermodynamical, geometrical and dynamical) are introduced, and the differences between the finite-size behaviour and the bulk behaviour are described. The phenomenon of "dynamical coexistence", which can be seen as the cluster spontaneously going back and forth between the solid and liquid states across the time, is illustrated. Its thermodynamical consequences are also emphasized. Finally, we present some typical thermodynamical phenomena due to the finite-size character, and strongly dependent on the physical chemistry of the matter at the microscopic level. We study these phenomena with Monte Carlo and molecular dynamics simulations: surface melting observed on rare gas clusters, multistage melting observed on ionic clusters, the special behaviours of molecular clusters, and the more intricate problem of free or solvated metallic clusters. La thermodynamique des agrégats est un sujet en développement croissant, tant sur le plan théorique qu'expérimental. Nous présentons un ensemble de méthodes théoriques et numériques destinées à l'étude des transitions de phase, en particulier de la transition solide-liquide, dans les agrégats atomiques et moléculaires. Divers moyens de caractérisation (thermodynamiques, géométriques et dynamiques) sont introduits, et les différences entre les comportements à taille finie et à taille macroscopique sont précisées. Le phénomène de "coexistence dynamique", qui voit l'agrégat passer spontanément de l'état solide à l'état liquide (et réciproquement) au cours du temps, est illustré, et ses conséquences thermodynamiques sont soulignées. Enfin, nous présentons un certain nombre de ph

  17. Unified phonon-based approach to the thermodynamics of solid, liquid and gas states

    NASA Astrophysics Data System (ADS)

    Bolmatov, Dima; Zav'yalov, Dmitry; Zhernenkov, Mikhail; Musaev, Edvard T.; Cai, Yong Q.

    2015-12-01

    We introduce a unified approach to states of matter (solid, liquid and gas) and describe the thermodynamics of the pressure-temperature phase diagram in terms of phonon excitations. We derive the effective Hamiltonian with low-energy cutoff in two transverse phonon polarizations (phononic band gaps) by breaking the symmetry in phonon interactions. Further, we construct the statistical mechanics of states of aggregation employing the Debye approximation. The introduced formalism covers the Debye theory of solids, the phonon theory of liquids, and thermodynamic limits such as the Dulong-Petit thermodynamic limit (cV = 3kB), the ideal gas limit (cV =3/2 kB) and the new thermodynamic limit (cV = 2kB), dubbed here the Frenkel line thermodynamic limit. We discuss the phonon propagation and localization effects in liquids above and below the Frenkel line, and explain the "fast sound" phenomenon. As a test for our theory we calculate velocity-velocity autocorrelation and pair distribution functions within the Green-Kubo formalism. We show the consistency between dynamics of phonons and pair correlations in the framework of the unified approach. New directions towards advancements in phononic band gaps engineering, hypersound manipulation technologies and exploration of exotic behaviour of fluids relevant to geo- and planetary sciences are discussed. The presented results are equally important both for practical implications and for fundamental research.

  18. Focused ultrasound solid-liquid extraction for the determination of organic biomarkers in beachrocks.

    PubMed

    Blanco-Zubiaguirre, L; Arrieta, N; Iturregui, A; Martinez-Arkarazo, I; Olivares, M; Castro, K; Olazabal, M A; Madariaga, J M

    2015-11-01

    Beachrocks are consolidated coastal sedimentary formations resulting mainly from the relative rapid cementation of beach sediments by different calcium carbonate polymorphs. Although previous works have already studied the elemental composition and the mineral phases composing these cements, few of them have focused their attention on the organic matter present therein. This work describes an extraction methodology based on focused ultrasound solid-liquid extraction (FUSLE), followed by analysis using large volume injection (LVI) in a programmable temperature vaporizer (PTV) combined with gas chromatography-mass spectrometry (GC-MS) in order to determine organics such as polycyclic aromatic hydrocarbons (PAHs) and biomarkers (hopanes), which can increase and confirm the information obtained so far. This goal has been achieved after the optimization of the main parameters affecting the extraction procedure, such as, extraction solvent, FUSLE variables (amplitude, extraction time and pulse time) and also variables affecting the LVI-PTV (vent time, injection speed and cryo-focusing temperature). The developed method rendered results comparable to traditional extraction methods in terms of accuracy (77-109%) and repeatability (RSD<23%). Finally, the analyses performed over real beachrock samples from the Bay of Biscay (Northern Spain) revealed the presence of the 16 EPA priority PAHs, as well as some organic biomarkers which could increase the knowledge about such beachrock formation. PMID:26186864

  19. Rapid heating of a strongly coupled plasma at the solid-liquid phase transition

    NASA Astrophysics Data System (ADS)

    Jensen, M. J.; Hasegawa, T.; Bollinger, J. J.; Dubin, D. H. E.

    2004-11-01

    Between 10^4 and 10^6 ^9Be^+ ions are trapped in a 4.5 Tesla Penning trap and laser-cooled to ˜1 mK, where the ions form a crystalline plasma with an interparticle spacing of ˜20 μm. This system is a realization of a strongly coupled one-component plasma. Using Doppler laser spectroscopy on a single-photon transition, we measured the temperature and heating rate of this plasma when not being laser-cooled. We measured a slow heating rate of ≤ 100 mK/s due to residual gas collisions for the first 100-200 ms after turning off the cooling laser. This slow heating is followed by a rapid heating to 1-2 K in 100 ms as the plasma undergoes the solid-liquid phase transition at T=10 mK (Γ ˜ 170). We will present evidence that this rapid heating is due to a sudden release of energy from weakly cooled degrees of freedom involving the cyclotron motion of trapped impurity ions. We will also discuss the prospects for observing the latent heat associated with the phase transition.

  20. Band offsets across solid-liquid interfaces from continuum solvation methods

    NASA Astrophysics Data System (ADS)

    Sundararaman, Ravishankar; Ping, Yuan; Galli, Giulia A.; Goddard, William A., III

    2015-03-01

    The band edge positions of photo-electrodes relative to water redox potentials play an important role in determining the efficiency of the photo-electrochemical cell. Direct theoretical calculations of solid-liquid interfaces are expensive and simplified models are desirable for rapid theoretical screening of new materials. However, traditional solvation models are extensively fit to describe organic solutes and hence extrapolate poorly to highly-polar inorganic surfaces. We develop minimally-empirical continuum solvation models suitable for treating such surfaces and present theoretical predictions of the band positions of rutile TiO2 (110) and WO3 (001) surfaces in water. We obtain non-negligible solvation effects ~ 1-2 eV, in good agreement with experimental results. This material is based upon work performed by the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, supported through the Office of Science of the U.S. Department of Energy under Award Number DE-SC0004993.

  1. Rheological Aspects of the Solid-Liquid Transition in Jammed Systems

    NASA Astrophysics Data System (ADS)

    Coussot, P.

    A common property of jammed systems is a yield stress they have to overcome in order to start to flow. In rheology it is generally assumed that the corresponding solid-liquid transition is continuous, the steady state viscosity progressively decreasing from infinity to a finite value as the applied shear stress is increased beyond the yield stress. Recent experiments with various materials such as colloidal suspensions, foams, emulsions, or polymer gels, show that this transition is in fact abrupt: in steady state, at a critical stress the material viscosity abruptly turns from infinity to a finite value. This phenomenon corresponds to another effect observed from MRI-rheometry tests: in steady state such pasty materials either flow at a sher rate larger than a critical, finite value, associated to a critical stress, or do not flow at all. This phenomenon has also a dynamic character, which is in particular illustrated by the "viscosity bifurcation" in time under controlled stress: below the critical stress value the shear rate progressively decreases until reaching stoppage; beyond this critical stress the shear rate increases and reaches a finite value. Moreover for a material initially at rest the interface between the sheared and unsheared regions, i.e. the slope break, progressively reaches its asymptotic position in time. From these results we deduce that usual macroscopic observations basically reflect complex space and time evolutions of flow and material characteristics in the rheometer gap, rather than local time-dependent properties.

  2. Simulations of solid-liquid friction at ice-Ih/water interfaces

    NASA Astrophysics Data System (ADS)

    Louden, Patrick B.; Gezelter, J. Daniel

    2013-11-01

    We have investigated the structural and dynamic properties of the basal and prismatic facets of the ice Ih/water interface when the solid phase is drawn through the liquid (i.e., sheared relative to the fluid phase). To impose the shear, we utilized a velocity-shearing and scaling approach to reverse non-equilibrium molecular dynamics. This method can create simultaneous temperature and velocity gradients and allow the measurement of transport properties at interfaces. The interfacial width was found to be independent of the relative velocity of the ice and liquid layers over a wide range of shear rates. Decays of molecular orientational time correlation functions gave similar estimates for the width of the interfaces, although the short- and longer-time decay components behave differently closer to the interface. Although both facets of ice are in "stick" boundary conditions in liquid water, the solid-liquid friction coefficients were found to be significantly different for the basal and prismatic facets of ice.

  3. Influence of dielectric properties on van der Waals/Casimir forces in solid-liquid systems

    SciTech Connect

    Zwol, P. J. van; Palasantzas, G.; De Hosson, J. Th. M.

    2009-05-15

    In this paper, we present calculations of van der Waals/Casimir forces, described by Lifshitz theory, for the solid-liquid-solid system using measured dielectric functions of all involved materials for the wavelength range from millimeters down to subnanometers. It is shown that even if the dielectric function is known over all relevant frequency ranges, the scatter in the dielectric data can lead to very large scatter in the calculated van der Waals/Casimir forces. Especially when the liquid dielectric function becomes comparable in magnitude to the dielectric function of one of the interacting solids, the associated variation in the force can be up to a factor of 2 for plate-plate separations 5-500 nm. This corresponds to an uncertainty up to 100% in the theory prediction for a specific system. As a result accuracy testing of the Lifshitz theory under these circumstances is rather questionable. Finally we discuss predictions of Lifshitz theory regarding multiple repulsive-attractive transitions with separation distance, as well as nontrivial scaling of the van der Waals/Casimir force with distance.

  4. How solid-liquid adhesive property regulates liquid slippage on solid surfaces?

    PubMed

    Xue, Yahui; Wu, Yang; Pei, Xiaowei; Duan, Huiling; Xue, Qunji; Zhou, Feng

    2015-01-13

    The influence of solid-liquid adhesive property on liquid slippage at solid surfaces has been investigated using experiment approach on well-defined model surfaces as well as theoretical analysis. Based on a classical molecular-kinetic description for molecular and hydrodynamic slip, we propose a simple theoretical model that directly relates the liquid slip length to the liquid adhesive force on solid surfaces, which yields an exponential decay function. Well-defined smooth surfaces with varied surface wettability/adhesion are fabricated by forming self-assembled monolayers on gold with different mole ratios of hydrophobic and hydrophilic thiols. The adhesive force of a water droplet and the molecular slippage on these surfaces are probed by surface force apparatus and quartz crystal microbalance measurements, respectively. The experiment results are well consistent with our theoretical prediction. Our finding benefits the understanding of the underlying mechanism of liquid slippage on solid surfaces at molecular level and the rational design of microfluidics with an aim to be frictionless or highly controllable. PMID:25511171

  5. Coarsening in Solid-liquid Mixtures: Overview of Experiments on Shuttle and ISS

    NASA Technical Reports Server (NTRS)

    Duval, Walter M. B.; Hawersaat, Robert W.; Lorik, T.; Thompson, J.; Gulsoy, B.; Voorhees, P. W.

    2013-01-01

    The microgravity environment on the Shuttle and the International Space Station (ISS) provides the ideal condition to perform experiments on Coarsening in Solid-Liquid Mixtures (CSLM) as deleterious effects such as particle sedimentation and buoyancy-induced convection are suppressed. For an ideal system such as Lead-Tin in which all the thermophysical properties are known, the initial condition in microgravity of randomly dispersed particles with local clustering of solid Tin in eutectic liquid Lead-Tin matrix, permitted kinetic studies of competitive particle growth for a range of volume fractions. Verification that the quenching phase of the experiment had negligible effect of the spatial distribution of particles is shown through the computational solution of the dynamical equations of motion, thus insuring quench-free effects from the coarsened microstructure measurements. The low volume fraction experiments conducted on the Shuttle showed agreement with transient Ostwald ripening theory, and the steady-state requirement of LSW theory was not achieved. More recent experiments conducted on ISS with higher volume fractions have achieved steady-state condition and show that the kinetics follows the classical diffusion limited particle coarsening prediction and the measured 3D particle size distribution becomes broader as predicted from theory.

  6. Enhanced mass transfer during solid liquid extraction of gamma-irradiated red beetroot

    NASA Astrophysics Data System (ADS)

    Nayak, Chetan A.; Chethana, S.; Rastogi, N. K.; Raghavarao, K. S. M. S.

    2006-01-01

    The exposure to gamma-irradiation pretreatment increases cell wall permeabilization, resulting in loss of turgor pressure, which led to the increase of extractability of betanin from red beetroot. The degree of extraction of betanin was investigated using gamma irradiation as a pretreatment prior to the solid-liquid extraction process and compared with control beetroot samples. The beetroot subjected to different doses of gamma irradiation (2.5, 5.0, 7.5, 10.0 kGy) and control was dipped in an acetic acid medium (1% v/v) to extract the betanin. The diffusion coefficients for betanin as well as ionic component were estimated considering Fickian diffusion. The results indicated an increase in the diffusion coefficient of betanin (0.302×10 -9-0.463×10 -9 m 2/s) and ionic component (0.248×10 -9-0.453×10 -9 m 2/s) as the dose rate increased (from 2.5 to 10.0 kGy). The degradation constant was found to increase (0.050-0.079 min -1) with an increase gamma-irradiation doses (2.5-10.0 kGy), indicating lower stability of the betanin as compared to control sample at 65 °C.

  7. Numerical formulation for the prediction of solid/liquid change of a binary alloy

    NASA Technical Reports Server (NTRS)

    Schneider, G. E.; Tiwari, S. N.

    1990-01-01

    A computational model is presented for the prediction of solid/liquid phase change energy transport including the influence of free convection fluid flow in the liquid phase region. The computational model considers the velocity components of all non-liquid phase change material control volumes to be zero but fully solves the coupled mass-momentum problem within the liquid region. The thermal energy model includes the entire domain and uses an enthalpy like model and a recently developed method for handling the phase change interface nonlinearity. Convergence studies are performed and comparisons made with experimental data for two different problem specifications. The convergence studies indicate that grid independence was achieved and the comparison with experimental data indicates excellent quantitative prediction of the melt fraction evolution. Qualitative data is also provided in the form of velocity vector diagrams and isotherm plots for selected times in the evolution of both problems. The computational costs incurred are quite low by comparison with previous efforts on solving these problems.

  8. Microscopic thin film optical anisotropy imaging at the solid-liquid interface

    NASA Astrophysics Data System (ADS)

    Miranda, Adelaide; De Beule, Pieter A. A.

    2016-04-01

    Optical anisotropy of thin films has been widely investigated through ellipsometry, whereby typically an optical signal is averaged over a ˜1 cm2 elliptical area that extends with increasing angle-of-incidence (AOI). Here, we report on spectroscopic imaging ellipsometry at the solid-liquid interface applied to a supported lipid bilayer (SLB). We detail how a differential spectrally resolved ellipsometry measurement, between samples with and without optically anisotropic thin film on an absorbing substrate, can be applied to recover in and out of plane refractive indices of the thin film with known film thickness, hence determining the thin film optical anisotropy. We also present how optimal wavelength and AOI settings can be determined ensuring low parameter cross correlation between the refractive indices to be determined from a differential measurement in Δ ellipsometry angle. Furthermore, we detail a Monte Carlo type analysis that allows one to determine the minimal required optical ellipsometry resolution to recover a given thin film anisotropy. We conclude by presenting a new setup for a spectroscopic imaging ellipsometry based on fiber supercontinuum laser technology, multi-wavelength diode system, and an improved liquid cell design, delivering a 5 ×-10 × ellipsometric noise reduction over state-of-the-art. We attribute this improvement to increased ellipsometer illumination power and a reduced light path in liquid through the use of a water dipping objective.

  9. Microscopic thin film optical anisotropy imaging at the solid-liquid interface.

    PubMed

    Miranda, Adelaide; De Beule, Pieter A A

    2016-04-01

    Optical anisotropy of thin films has been widely investigated through ellipsometry, whereby typically an optical signal is averaged over a ∼1 cm(2) elliptical area that extends with increasing angle-of-incidence (AOI). Here, we report on spectroscopic imaging ellipsometry at the solid-liquid interface applied to a supported lipid bilayer (SLB). We detail how a differential spectrally resolved ellipsometry measurement, between samples with and without optically anisotropic thin film on an absorbing substrate, can be applied to recover in and out of plane refractive indices of the thin film with known film thickness, hence determining the thin film optical anisotropy. We also present how optimal wavelength and AOI settings can be determined ensuring low parameter cross correlation between the refractive indices to be determined from a differential measurement in Δ ellipsometry angle. Furthermore, we detail a Monte Carlo type analysis that allows one to determine the minimal required optical ellipsometry resolution to recover a given thin film anisotropy. We conclude by presenting a new setup for a spectroscopic imaging ellipsometry based on fiber supercontinuum laser technology, multi-wavelength diode system, and an improved liquid cell design, delivering a 5 ×-10 × ellipsometric noise reduction over state-of-the-art. We attribute this improvement to increased ellipsometer illumination power and a reduced light path in liquid through the use of a water dipping objective. PMID:27131681

  10. Solid-liquid interface free energies of pure bcc metals and B2 phases

    DOE PAGESBeta

    Wilson, S. R.; Gunawardana, K. G. S. H.; Mendelev, M. I.

    2015-04-07

    The solid-liquid interface (SLI) free energy was determined from molecular dynamics (MD) simulation for several body centered cubic (bcc) metals and B2 metallic compounds (space group: Pm3¯m ; prototype: CsCl). In order to include a bcc metal with a low melting temperature in our study, a semi-empirical potential was developed for Na. Two additional synthetic “Na” potentials were also developed to explore the effect of liquid structure and latent heat on the SLI free energy. The obtained MD data were compared with the empirical Turnbull, Laird, and Ewing relations. All three relations are found to predict the general trend observedmore » in the MD data for bcc metals obtained within the present study. However, only the Laird and Ewing relations are able to predict the trend obtained within the sequence of “Na” potentials. The Laird relation provides the best prediction for our MD data and other MD data for bcc metals taken from the literature. Overall, the Laird relation also agrees well with our B2 data but requires a proportionality constant that is substantially different from the bcc case. It also fails to explain a considerable difference between the SLI free energies of some B2 phases which have nearly the same melting temperature. In contrast, this difference is satisfactorily described by the Ewing relation. Thus, the Ewing relation obtained from the bcc dataset also provides a reasonable description of the B2 data.« less

  11. Solid-liquid interface free energies of pure bcc metals and B2 phases

    SciTech Connect

    Wilson, S. R.; Gunawardana, K. G. S. H.; Mendelev, M. I.

    2015-04-07

    The solid-liquid interface (SLI) free energy was determined from molecular dynamics (MD) simulation for several body centered cubic (bcc) metals and B2 metallic compounds (space group: Pm3¯m ; prototype: CsCl). In order to include a bcc metal with a low melting temperature in our study, a semi-empirical potential was developed for Na. Two additional synthetic “Na” potentials were also developed to explore the effect of liquid structure and latent heat on the SLI free energy. The obtained MD data were compared with the empirical Turnbull, Laird, and Ewing relations. All three relations are found to predict the general trend observed in the MD data for bcc metals obtained within the present study. However, only the Laird and Ewing relations are able to predict the trend obtained within the sequence of “Na” potentials. The Laird relation provides the best prediction for our MD data and other MD data for bcc metals taken from the literature. Overall, the Laird relation also agrees well with our B2 data but requires a proportionality constant that is substantially different from the bcc case. It also fails to explain a considerable difference between the SLI free energies of some B2 phases which have nearly the same melting temperature. In contrast, this difference is satisfactorily described by the Ewing relation. Thus, the Ewing relation obtained from the bcc dataset also provides a reasonable description of the B2 data.

  12. Solid-liquid separation of oxidized americium from fission product lanthanides

    NASA Astrophysics Data System (ADS)

    Shehee, T. C.; Martin, L. R.; Nash, K. L.

    2010-03-01

    The separation of americium from the lanthanides and curium is a requirement if transmutation of americium is to be performed in advanced nuclear fuel cycles. Oxidation of Am3+ to AmO2+ or AmO22+ may allow separation of Am from Ln and Cm in one step, since the lanthanides and curium do not have higher oxidation states as accessible. Two possible solid-liquid separation methods have been developed to address this difficult separation. Under acidic conditions using oxone or persulfate, the oxidation and retention of tracer Am in the aqueous phase has been observed with a separation factor of 11 ± 1. Most of these studies have been conducted using 237NpO2(NO3), 233UO2(NO3)2, 238Pu(NO3)4 and 241Am(NO3)3 at radiotracer concentrations. Lanthanides precipitate as the sodium or potassium europium double sulfate salt. Under basic conditions, ozone oxidation of Am(CO3)OH(s) solubilizes Am from a lanthanide carbonate hydroxide solid phase to the aqueous phase as the AmO2(CO3)34-or AmO2(CO3)35- species. For the ozone oxidation of the americium tracer a separation factor of 1.6 ± 0.8 and 47 ± 2 for the oxidation/separation in Na2CO3 and NaHCO3 respectively.

  13. The impact of algal properties and pre-oxidation on solid-liquid separation of algae.

    PubMed

    Henderson, Rita; Parsons, Simon A; Jefferson, Bruce

    2008-04-01

    Algae are traditionally classified according to biological descriptors which do not give information on surface characteristics that are important with respect to removal by water treatment processes. This review examines the character of freshwater algal populations from a water treatment perspective and evaluates the impact of their varying properties and the use of pre-oxidation on their removal by solid-liquid separation processes.. The characteristics shown to impact on treatment were morphology, motility, surface charge, cell density and the extracellular organic matter (EOM) composition and concentration. With the exception of density, these are not phyla specific. It was also shown that dissolved air flotation (DAF) was the most robust clarification method, where up to 99.8% removal was achieved compared to 94% for sedimentation when using metal coagulants. However, successful clarification relied heavily on the optimisation of preceding coagulation and flocculation and coagulant demand was important in this respect. Comparison of all available data reveals a relationship between cell surface area and coagulant demand. It is thus suggested that cell surface area would provide a basis for regrouping algae such that the classification is informative with respect to water treatment. However, the absolute coagulant demand is a result of both surface area and EOM influences. The latter are relatively poorly understood in comparison to natural organic matter (NOM) systems and this remains a limit in current knowledge. PMID:18261761

  14. Measurements of Solid-Liquid Interfacial Energies in the Organic Monotectic Alloys

    NASA Astrophysics Data System (ADS)

    Böyük, U.; Yüceer, K.; Keşlioğlu, K.; Ulgen, A.; Maraşli, N.

    The commercial purity dibromobenzene (DBB) and succinonitrile (SCN) were purified using a columnar distillation system. Thin walled rectangular specimen cells (60-80 μm thick) were fabricated and filled with the purified materials under the vacuum. The specimen cell was placed in a horizontal temperature gradient stage. A thin liquid layer was melted and the specimen was annealed in a constant temperature gradient for an enough time to observe the equilibrated grain boundary groove shapes. The thermal conductivities of solid and liquid phases for the purified DBB and DBB-5.7 mol% SCN alloy were determined with the radial heat flow and the Bridgman-type growth apparatuses. From the observed grain boundary groove shapes, the Gibbs-Thomson coefficients, solid-liquid interfacial energies, and the grain boundary energies for solid DBB in equilibrium with its melts and solid DBB in equilibrium with DBB-SCN monotectic liquid have been determined. The temperature coefficients of the purified DBB and DBB-5.7 mol% SCN alloy were also determined from thermal conductivity curve vs temperature.

  15. Measurement of solid-liquid interfacial energy in the pyrene succinonitrile monotectic system.

    PubMed

    Akbulut, S; Ocak, Y; Böyük, U; Erol, M; Keşlioğlu, K; Maraşli, N

    2006-09-20

    The equilibrated grain boundary groove shapes for solid pyrene (PY) in equilibrium with the PY succinonitrile (SCN) monotectic liquid were directly observed. From the observed grain boundary groove shapes, the Gibbs-Thomson coefficient and solid-liquid interfacial energy for solid PY in equilibrium with the PY SCN monotectic liquid have been determined to be (8.72 ± 0.87) × 10(-8) K m and (21.9 ± 3.28) × 10(-3) J m(-2) with the present numerical method and Gibbs-Thomson equation, respectively. The grain boundary energy of the solid PY phase has been determined to be (42.84 ± 7.28) × 10(-3) J m(-2) from the observed grain boundary groove shapes. Thermal conductivities of solid and liquid phases for PY-2.5 mol% SCN alloy and pure PY have also been measured. PMID:21690896

  16. Coarsening in Solid-Liquid Mixtures-2: A Materials Science Experiment for the ISS

    NASA Technical Reports Server (NTRS)

    Hickman, J. Mark; Voorhees, Peter W.; Kwon, Yongwoo; Lorik, Tibor

    2004-01-01

    A materials science experiment has been developed and readied for operation aboard the International Space Station (ISS). Components of this experiment are onboard ISS and area awaiting the flight of science samples. The goal of the experiment is to understand the dynamics of Ostwald ripening, also known as coarsening, a process that occurs in nearly any two-phase mixture found in nature. Attempts to obtain experimental data in ground-based laboratories are hindered due to the presence of gravity, which introduces material transport modes other than that of the coarsening phenomenon. This introduces adjustable parameters in the formulation of theory. The original Coarsening in Solid-Liquid Mixtures (CSLM) mission, which flew on the Space Shuttle in 1997, produced data from a coarsened eutectic alloy. Unfortunately, both the science matrix and the hardware, while nominally functional, did not account adequately for operations in microgravity. A significantly redesigned follow-on experiment, CSLM-2 has been developed to redress the inadequacies of the original experiment. This paper reviews the CSLM-2 project: its history, science goals, flight hardware implementation, and planned operations and analysis

  17. Biodegradation of Endocrine Disruptors in Solid-Liquid Two-Phase Partitioning Systems by Enrichment Cultures

    PubMed Central

    dos Santos, Silvia Cristina Cunha; Ouellette, Julianne; Juteau, Pierre; Lépine, François; Déziel, Eric

    2013-01-01

    Naturally occurring and synthetic estrogens and other molecules from industrial sources strongly contribute to the endocrine disruption of urban wastewater. Because of the presence of these molecules in low but effective concentrations in wastewaters, these endocrine disruptors (EDs) are only partially removed after most wastewater treatments, reflecting the presence of these molecules in rivers in urban areas. The development of a two-phase partitioning bioreactor (TPPB) might be an effective strategy for the removal of EDs from wastewater plant effluents. Here, we describe the establishment of three ED-degrading microbial enrichment cultures adapted to a solid-liquid two-phase partitioning system using Hytrel as the immiscible water phase and loaded with estrone, estradiol, estriol, ethynylestradiol, nonylphenol, and bisphenol A. All molecules except ethynylestradiol were degraded in the enrichment cultures. The bacterial composition of the three enrichment cultures was determined using 16S rRNA gene sequencing and showed sequences affiliated with bacteria associated with the degradation of these compounds, such as Sphingomonadales. One Rhodococcus isolate capable of degrading estrone, estradiol, and estriol was isolated from one enrichment culture. These results highlight the great potential for the development of TPPB for the degradation of highly diluted EDs in water effluents. PMID:23728808

  18. Visual investigation of solid-liquid phase equilibria for nonflammable mixed refrigerant

    NASA Astrophysics Data System (ADS)

    Lee, C.; Yoo, J.; Park, I.; Park, J.; Cha, J.; Jeong, S.

    2015-12-01

    Non-flammable mixed refrigerant (NF-MR) Joule Thomson (J-T) refrigerators have desirable characteristics and wide cooling temperature range compared to those of pure J-T refrigerators. However, the operating challenge due to freezing is a critical issue to construct this refrigerator. In this paper, the solid-liquid phase equilibria (i.e. freezing point) of the NF-MR which is composed of Argon, R14 (CF4), and R218 (C3F8), has been experimentally investigated by a visualized apparatus. Argon, R14 and R218 mixtures are selected to be effectively capable of reaching 100 K in the MR J-T refrigerator system. Freezing points of the mixtures have been measured with the molar compositions from 0.1 to 0.8 for each component. Each test result is simultaneously acquired by a camcorder for visual inspection and temperature measurement during a warming process. Experimental results show that the certain mole fraction of Argon, R14, and R218 mixture can achieve remarkably low freezing temperature even below 77 K. This unusual freezing point depression characteristic of the MR can be a useful information for designing a cryogenic MR J-T refrigerator to reach further down to 77 K.

  19. Visualization of the solid-liquid equilibria for non-flammable mixed refrigerants

    NASA Astrophysics Data System (ADS)

    Lee, Cheonkyu; Yoo, Junghyun; Lee, Jisung; Jeong, Sangkwon

    2016-04-01

    Non-flammable mixed refrigerant (NF-MR) Joule Thomson (J-T) refrigerators have desirable characteristics and wide cooling temperature range compared to those of pure J-T refrigerators. However, the operating challenge due to freezing is a critical issue to realize this type of refrigerator. In this paper, the solid-liquid phase equilibria (i.e. freezing point) of the NF-MR which is composed of Argon (Ar), R14 (CF4), and R218 (C3F8), has been experimentally investigated by a visualized apparatus. The accuracy of the apparatus is experimentally verified with pure refrigerants and selected binary mixed refrigerants. Freezing points of the ternary NF-MRs have been measured with the molar compositions from 0.1 to 0.8 for each component. Each test result is simultaneously acquired by a camcorder for visual inspection and temperature measurement during a warming process. Experimental results reveal that the specific MR, with R14 molar composition higher than 0.4, can achieve remarkably low freezing temperature even below 77 K. These unusual freezing point depression characteristics of the MR can be a useful information for designing a cryogenic MR J-T refrigerator to reach temperatures less than 77 K.

  20. Molecular Dynamics Study of Freezing Point and Solid-Liquid Interfacial Free Energy of Stockmayer Fluids

    SciTech Connect

    Wang, J.; Apte, Pankaj; Morris, James R; Zeng, X.C.

    2013-01-01

    Freezing temperatures of Stockmayer fluids with different dipolar strength at zero pressure are estimated and computed using three independent molecular-dynamics (MD) simulation methods, namely, the superheating-undercooling method, the constant-pressure and constant-temperature (NPT) two phase coexistence method, and the constant-pressure and constant-enthalpy (NPH) coexistence method. The best estimate of the freezing temperature (in reduced unit) for the Stockmayer (SM) fluid with a reduced dipole moment is 0.656 0.001, 0.726 0.002 and 0.835 0.005, respectively. The freezing temperature increases with the dipolar strength. The solid-liquid interfacial free energies of the (111), (110) and (100) interface are calculated for the first time using two independent methods, namely, the cleaving-wall method and the interfacial fluctuation method. Both methods predict that the interfacial free energy increases with the dipole moment. Although the interfacial fluctuation method suggests a weaker interfacial anisotropy, particularly for strongly dipolar SM fluids, both methods predicted the same trend of interfacial anisotropy, that is, .

  1. Research on the pattern of solid-liquid two-phase distribution in chemical process pump

    NASA Astrophysics Data System (ADS)

    Liu, Y.; Jiang, Y.; Han, Z. J.

    2012-11-01

    In order to explore the pattern of solid-liquid two-phase flow distribution in first stage of double-suction impeller and the double volute channel of the HD type petrol-chemical process pump, the flow field in double-suction impeller and double volute is simulated with the CFD software, by taking the Reynolds Averaged Navier Stokes equations as its governing equations, and the standard k-ε model for turbulence, derives the pattern of solid particle concentration distribution in the impeller and double volute channel under different initial particle concentrations and different particle diameters. The results show that in the double-suction impeller, solid phase distribution changes a lot along with the increase of initial particle concentration; the concentration near the back side is higher than the face side. Solid particles have the motion trend to the back side of blade in double-suction impeller along with the increase of particle diameters. In double volute channel, solid phase concentration distribution is uneven and solid particle concentration is relatively higher from section 1 to section 8. In the diffusion section, concentration is high in lateral side and low in medial side, the solid particles have the motion trend to the lateral side and the solid particle concentration is relatively higher.

  2. Solid/liquid extraction equilibria of phenolic compounds with trioctylphosphine oxide impregnated in polymeric membranes.

    PubMed

    Praveen, Prashant; Loh, Kai-Chee

    2016-06-01

    Trioctylphosphine oxide based extractant impregnated membranes (EIM) were used for extraction of phenol and its methyl, hydroxyl and chloride substituted derivatives. The distribution coefficients of the phenols varied from 2 to 234, in the order of 1-napthol > p-chlorophenol > m-cresol > p-cresol > o-cresol > phenol > catechol > pyrogallol > hydroquinone, when initial phenols loadings was varied in 100-2000 mg/L. An extraction model, based on the law of mass action, was formulated to predict the equilibrium distribution of the phenols. The model was in excellent agreement (R(2) > 0.97) with the experimental results at low phenols concentrations (<800 mg/L). At higher phenols loadings though, Langmuir isotherm was better suited for equilibrium prediction (R(2) > 0.95), which signified high mass transfer resistance in the EIMs. Examination of the effects of ring substitution on equilibrium, and bivariate statistical analysis between the amounts of phenols extracted into the EIMs and factors affecting phenols interaction with TOPO, indicated the dominant role of hydrophobicity in equilibrium determination. These results improve understanding of the solid/liquid equilibrium process between phenols and the EIMs, and these will be useful in designing phenol recovery process from wastewater. PMID:27031803

  3. Vapor-Induced Solid-Liquid-Solid Process for Silicon-based Nanowire Growth

    SciTech Connect

    Zhang, Jiguang; Liu, Jun; Wang, Donghai; Choi, Daiwon; Fifield, Leonard S.; Wang, Chong M.; Xia, Guanguang; Nie, Zimin; Yang, Zhenguo; Pederson, Larry R.; Graff, Gordon L.

    2010-03-10

    Silicon based nanowires have been grown from commercial silicon powders under conditions of differing oxygen and carbon activities. Nanowires grown in the presence of carbon sources consisted of a crystalline SiC core with an amorphous SiOx shell. The thickness of SiOx shell decreased as the oxygen concentration in the precursor gases was lowered. Nanowires grown in a carbon-free environment consisted of amorphous silicon oxide with a typical composition of SiO1.8. The growth rate of nanowires decreased with decreasing oxygen content in the precursor gases. SiO1.8 nanowires exhibited an initial discharge capacity of ~ 1,300 mAh/g and better stability than those of silicon powders. A Vapor Induced Solid-Liquid-Solid (VI-SLS) mechanism is proposed to explain the nanowire growth (including silicon and other metal based nanowires) from powder sources. In this approach, both a gas source and a solid powder source are required for nanowire growth. This mechanism is consistent with experimental observations and can also be used to guide the design and growth of other nanowires.

  4. DETERMINATION OF SOLID-LIQUID EQUILIBRIA DATA FOR MIXTURES OF HEAVY HYDROCARBONS IN A LIGHT SOLVENT

    SciTech Connect

    F.V. Hanson; J.V. Fletcher; Karthik R.

    2003-06-01

    A methodology was developed using an FT-IR spectroscopic technique to obtain solid-liquid equilibria (SLE) data for mixtures of heavy hydrocarbons in significantly lighter hydrocarbon diluents. SLE was examined in multiple Model Oils that were assembled to simulate waxes. The various Model oils were comprised of C-30 to C-44 hydrocarbons in decane. The FT-IR technique was used to identify the wax precipitation temperature (WPT). The DSC technique was also used in the identification of the onset of the two-phase equilibrium in this work. An additional Model oil made up of C-20 to C-30 hydrocarbons in decane was studied using the DSC experiment. The weight percent solid below the WPT was calculated using the FT-IR experimental results. The WPT and the weight percent solid below the WPT were predicted using an activity coefficient based thermodynamic model. The FT-IR spectroscopy method is found to successfully provide SLE data and also has several advantages over other laboratory-based methods.

  5. High Frequency Acoustic Reflectometry for Solid/Liquid Interface Characterization: Application to Droplet Evaporation

    NASA Astrophysics Data System (ADS)

    Carlier, Julien; Toubal, Malika; Li, Sizhe; Campistron, Pierre; Callens, Dorothée; Thomy, Vincent; Senez, Vincent; Nongaillard, Bertrand

    Evolution of the local concentration in a 1 μL droplet of ethanol/water mixture during an evaporation process has been followed using high frequency acoustic reflectometry. This method has been developed for wetting characterization on micro/nanostructures and makes it possible to follow concentration evolution in a droplet deposited on a solid surface. This information gives the opportunity to predict wetting depending on surface tension linked to alcohol concentration evolution. The calibration of the method and concentration evolution in 50% and 30% ethanol droplets are presented. The evolution of a pure ethanol droplet composition is tracked so as to follow hydration process.

  6. Hot Electrons at Solid-Liquid Interfaces: A Large Chemoelectric Effect during the Catalytic Decomposition of Hydrogen Peroxide.

    PubMed

    Nedrygailov, Ievgen I; Lee, Changhwan; Moon, Song Yi; Lee, Hyosun; Park, Jeong Young

    2016-08-26

    The study of energy and charge transfer during chemical reactions on metals is of great importance for understanding the phenomena involved in heterogeneous catalysis. Despite extensive studies, very little is known about the nature of hot electrons generated at solid-liquid interfaces. Herein, we report remarkable results showing the detection of hot electrons as a chemicurrent generated at the solid-liquid interface during decomposition of hydrogen peroxide (H2 O2 ) catalyzed on Schottky nanodiodes. The chemicurrent reflects the activity of the catalytic reaction and the state of the catalyst in real time. We show that the chemicurrent yield can reach values up to 10(-1) electrons/O2 molecule, which is notably higher than that for solid-gas reactions on similar nanodiodes. PMID:27374493

  7. In-drop capillary spooling of spider capture thread inspires hybrid fibers with mixed solid-liquid mechanical properties.

    PubMed

    Elettro, Hervé; Neukirch, Sébastien; Vollrath, Fritz; Antkowiak, Arnaud

    2016-05-31

    An essential element in the web-trap architecture, the capture silk spun by ecribellate orb spiders consists of glue droplets sitting astride a silk filament. Mechanically this thread presents a mixed solid-liquid behavior unknown to date. Under extension, capture silk behaves as a particularly stretchy solid, owing to its molecular nanosprings, but it totally switches behavior in compression to now become liquid-like: It shrinks with no apparent limit while exerting a constant tension. Here, we unravel the physics underpinning the unique behavior of this "liquid wire" and demonstrate that its mechanical response originates in the shape-switching of the silk filament induced by buckling within the droplets. Learning from this natural example of geometry and mechanics, we manufactured programmable liquid wires that present previously unidentified pathways for the design of new hybrid solid-liquid materials. PMID:27185930

  8. Study of the generation characteristics of laser converters with dye-based wide-aperture solid--liquid active elements

    SciTech Connect

    Eremenko, A.S.; Zemskii, V.I.; Kolesnikov, Y.L.; Malinin, B.G.; Meshkovsky, I.K.; Savkin, N.P.; Stepanov, V.E.; Shildyaev, V.S.

    1986-11-01

    The lasing characteristics of an active element, consisting of a fine porous silicate matrix, has been studied. Molecules of a dye (rhodamine 6G) and an ethanol solution of the same dye were introduced into the cells. It has been shown that under conditions of large heat release (when thermooptical distortions begin to appear in the dye solutions), the solid--liquid element preserves the stability of its own lasing characteristics.

  9. ZnO nanoneedle/H2O solid-liquid heterojunction-based self-powered ultraviolet detector

    PubMed Central

    2013-01-01

    ZnO nanoneedle arrays were grown vertically on a fluorine-doped tin oxide-coated glass by hydrothermal method at a relatively low temperature. A self-powered photoelectrochemical cell-type UV detector was fabricated using the ZnO nanoneedles as the active photoanode and H2O as the electrolyte. This solid-liquid heterojunction offers an enlarged ZnO/water contact area and a direct pathway for electron transport simultaneously. By connecting this UV photodetector to an ammeter, the intensity of UV light can be quantified using the output short-circuit photocurrent without a power source. High photosensitivity, excellent spectral selectivity, and fast photoresponse at zero bias are observed in this UV detector. The self-powered behavior can be well explained by the formation of a space charge layer near the interface of the solid-liquid heterojunction, which results in a built-in potential and makes the solid-liquid heterojunction work in photovoltaic mode. PMID:24103153

  10. A molecular dynamics study to determine the solid-liquid interfacial tension using test area simulation method (TASM)

    NASA Astrophysics Data System (ADS)

    Nair, Anjan R.; Sathian, Sarith P.

    2012-08-01

    Molecular dynamics (MD) studies on heat transfer from a heated nanoparticle into the surrounding fluid have indicated that the fluid next to a spherical nanoparticle can get heated well above its boiling point without observing a phase change, while a contradicting behavior was observed for a flat surface-fluid interface. Another interesting observation is that the critical heat flux was found to increase with increase in the wetting characteristics of solid. Thus, the interfacial tension or free energy of solid-liquid interface could play a pivotal role in the mechanism of heat transfer. A recent study by Gloor et al. [J. Chem. Phys. 123, 134703 (2005)], 10.1063/1.2038827 has proposed test area simulation method (TASM) for the determination of interfacial tension. The present study involves the determination and the comparison of solid-liquid interfacial tension for planar and spherical interfaces using MD based on TASM and analyze the results. A higher interfacial tension value is observed for spherical nanoparticle fluid interface compared to flat surface fluid interface. The results also indicate that the solid-liquid interfacial tension is a size and temperature dependent property. The results from this study are also expected to give better insights into the possible reasons for the observed differences in the thermal transport for spherical nanoparticle-liquid interface compared to planar-liquid interface.

  11. Thermodynamic and rheological properties of solid-liquid systems in coal processing. Quarterly technical report, October 1--December 31, 1994

    SciTech Connect

    Kabadi, V.N.; Ilias, S.

    1995-10-01

    The objective of this project is to develop a model for solid-liquid equilibria and a model for viscosities of the products of coal liquefaction processes. The same characterization procedure and representation by continuous distributions as used in previous work on vapor-liquid equilibria and excess enthalpies of coal liquids will be used. Models when fully developed will give the solid-liquid phase equilibrium properties and viscosities as factors of temperature and pressure for known molecular weight distribution and structural characterization of the coal liquid. To accomplish this well, the project requires three tasks: (1) Solid-Liquid phase equilibrium model development; (2) Experimental Viscosity Measurements; and (3) Viscosity Model Development. The work on development of a predictive model for saturated liquid volumes of coal model compounds has been completed. A manuscript has been prepared for submission to AIChE Journal. A copy of the manuscript is attached. Work on extending the viscosity model to coal derived liquids is continuing and progress on this work will be included in the next report.

  12. A bottom-up approach to understanding protein layer formation at solid-liquid interfaces.

    PubMed

    Kastantin, Mark; Langdon, Blake B; Schwartz, Daniel K

    2014-05-01

    A common goal across different fields (e.g. separations, biosensors, biomaterials, pharmaceuticals) is to understand how protein behavior at solid-liquid interfaces is affected by environmental conditions. Temperature, pH, ionic strength, and the chemical and physical properties of the solid surface, among many factors, can control microscopic protein dynamics (e.g. adsorption, desorption, diffusion, aggregation) that contribute to macroscopic properties like time-dependent total protein surface coverage and protein structure. These relationships are typically studied through a top-down approach in which macroscopic observations are explained using analytical models that are based upon reasonable, but not universally true, simplifying assumptions about microscopic protein dynamics. Conclusions connecting microscopic dynamics to environmental factors can be heavily biased by potentially incorrect assumptions. In contrast, more complicated models avoid several of the common assumptions but require many parameters that have overlapping effects on predictions of macroscopic, average protein properties. Consequently, these models are poorly suited for the top-down approach. Because the sophistication incorporated into these models may ultimately prove essential to understanding interfacial protein behavior, this article proposes a bottom-up approach in which direct observations of microscopic protein dynamics specify parameters in complicated models, which then generate macroscopic predictions to compare with experiment. In this framework, single-molecule tracking has proven capable of making direct measurements of microscopic protein dynamics, but must be complemented by modeling to combine and extrapolate many independent microscopic observations to the macro-scale. The bottom-up approach is expected to better connect environmental factors to macroscopic protein behavior, thereby guiding rational choices that promote desirable protein behaviors. PMID:24484895

  13. Solid-liquid separation by sonochemistry: a new approach for the separation of mineral suspensions.

    PubMed

    Nakamura, Takashi; Okawa, Hirokazu; Kawamura, Youhei; Sugawara, Katsuyasu

    2011-01-01

    The effect of sonochemistry to acidify solutions was applied for the solid-liquid separation of three kinds of mineral suspensions. At first, the relationship was measured between zeta-potential and pH in these suspensions to find pH levels correspondent to the isoelectric points. Then sonication (200 kHz or 28 kHz) was applied to adjust pH to the isoelectric points and separated particles from solutions by still-standing and spontaneous precipitation. Compared to the conventional methods using filters and chemical agents, the advantage of this sonochemical separation is two-fold. First, it does not require the maintenance of filters. Second, separated particles are easy to use since they are not mixed with pH adjusters and chemical flocculants. Isoelectric zone (ion strength 0.01, concentration 0.001 wt.%) of green tuff, andesite and titanium dioxide suspensions tested in this study were pH 1.1-3.7, 0.8-3.4, 2.7-5.7, respectively. The sonication of green tuff and andesite suspensions at 200 kHz changed the pH to the isoelectric zone despite the pH buffering effect of eluted alkali earth metals, and successfully precipitated the particles. On the contrary, the sonication of these suspensions at 28 kHz failed to adjust pH to the isoelectric zone, and the particles did not precipitate. In addition, the degradation of particles was observed in the SEM photographs of particles sonicated at 28 kHz, whereas no significant change was detected in particles sonicated at 200 kHz. Thus, it is concluded that the optimal frequency is about 200 kHz because its strong chemical effect can easily adjust the pH while its relatively weak physical effect prevents the degradation of particles. PMID:20643570

  14. Linear morphological stability analysis of the solid-liquid interface in rapidsolidification of a binary system

    NASA Astrophysics Data System (ADS)

    Galenko, P. K.; Danilov, D. A.

    2004-05-01

    The interface stability against small perturbations of the planar solid-liquid interface is considered analytically in linear approximation. Following the analytical procedure of Trivedi and Kurz [

    R. Trivedi and W. Kurz, Acta Metall. 34, 1663 (1986)
    ], which is advancing the original treatment of morphological stability by Mullins and Sekerka [
    W. W. Mullins and R. F. Sekerka, J. Appl. Phys. 35, 444 (1964)
    ] to the case of rapid solidification, we extend the model by introducing the local nonequilibrium in the solute diffusion field around the interface. A solution to the heat- and mass-transport problem around the perturbed interface is given in the presence of the local nonequilibrium solute diffusion. Using the developing local nonequilibrium model of solidification, the self-consistent analysis of linear morphological stability is presented with the attribution to the marginal (neutral) and absolute morphological stability of a rapidly moving interface. Special consideration of the interface stability for the cases of solidification in negative and positive thermal gradients is given. A quantitative comparison of the model predictions for the absolute morphological stability is presented with regard to experimental results of Hoglund and Aziz [ D. E. Hoglund and M. J. Aziz, in Kinetics of Phase Transformations, edited by M.O. Thompson, M. J. Aziz, and G. B. Stephenson, MRS Symposia Proceedings No. 205 (Materials Research Society, Pittsburgh, 1991), p. 325 ] on critical solute concentration for the interface breakdown during rapid solidification of Si-Sn alloys.

  15. Performance Validation and Scaling of a Capillary Membrane Solid-Liquid Separation System

    SciTech Connect

    Rogers, S; Cook, J; Juratovac, J; Goodwillie, J; Burke, T

    2011-10-25

    Algaeventure Systems (AVS) has previously demonstrated an innovative technology for dewatering algae slurries that dramatically reduces energy consumption by utilizing surface physics and capillary action. Funded by a $6M ARPA-E award, transforming the original Harvesting, Dewatering and Drying (HDD) prototype machine into a commercially viable technology has required significant attention to material performance, integration of sensors and control systems, and especially addressing scaling issues that would allow processing extreme volumes of algal cultivation media/slurry. Decoupling the harvesting, dewatering and drying processes, and addressing the rate limiting steps for each of the individual steps has allowed for the development individual technologies that may be tailored to the specific needs of various cultivation systems. The primary performance metric used by AVS to assess the economic viability of its Solid-Liquid Separation (SLS) dewatering technology is algae mass production rate as a function of power consumption (cost), cake solids/moisture content, and solids capture efficiency. An associated secondary performance metric is algae mass loading rate which is dependent on hydraulic loading rate, area-specific hydraulic processing capacity (gpm/in2), filter:capillary belt contact area, and influent algae concentration. The system is capable of dewatering 4 g/L (0.4%) algae streams to solids concentrations up to 30% with capture efficiencies of 80+%, however mass production is highly dependent on average cell size (which determines filter mesh size and percent open area). This paper will present data detailing the scaling efforts to date. Characterization and performance data for novel membranes, as well as optimization of off-the-shelf filter materials will be examined. Third party validation from Ohio University on performance and operating cost, as well as design modification suggestions will be discussed. Extrapolation of current productivities

  16. Experimental studies on irreversibility of electrostatic adsorption of silica nanoparticles at solid-liquid interface.

    PubMed

    Li, Xue; Niitsoo, Olivia; Couzis, Alexander

    2014-04-15

    Adsorption of colloidal nanoparticles (NPs) at solid-liquid interface is a scientifically interesting and technologically important phenomenon due to its fundamental importance in many industrial, environmental, and biological processes, such as wastewater treatment, printing, coating of surfaces, chromatography, papermaking, or biocompatibility. The process is well understood theoretically by the random sequential adsorption (RSA) model, based on the assumption of irreversible adsorption. Irreversible adsorption is defined as a process in which, once adsorbed, a particle can neither desorb, nor to move laterally on the surface. However, published experimental data that verifies the irreversibility of particle adsorption are very limited. In this study, we demonstrate the irreversibility of electrostatically driven nanoparticle adsorption utilizing a carefully selected set of experiments. A simple method was employed by uniquely introducing Ag@SiO2 core/shell NPs to perform exchange adsorptions experiments. Stöber SiO2 NPs with a diameter of 50-80 nm were initially electrostatically adsorbed onto amino-functionalized silicon wafer substrates followed by the subsequent adsorption of Ag@SiO2 NPs. The Ag@SiO2 NPs have the same surface chemistry as the neat SiO2 NPs. For the second step the adsorption time was varied from 1 min to 1 week so as to get a thorough understanding of the process irreversibility. Surface coverage quantification has shown that the surface coverage of the initially adsorbed SiO2 NPs stays the same independent of the duration of the second step adsorption using the Ag@SiO2 core/shell NPs. This observation directly confirms the irreversibility of electrostatic adsorption of NPs. PMID:24559699

  17. Universality and criticality of a second-order granular solid-liquid-like phase transition

    NASA Astrophysics Data System (ADS)

    Castillo, Gustavo; Mujica, Nicolás; Soto, Rodrigo

    2015-01-01

    We experimentally study the critical properties of the nonequilibrium solid-liquid-like transition that takes place in vibrated granular matter. The critical dynamics is characterized by the coupling of the density field with the bond-orientational order parameter Q4, which measures the degree of local crystallization. Two setups are compared, which present the transition at different critical accelerations as a result of modifying the energy dissipation parameters. In both setups five independent critical exponents are measured, associated to different properties of Q4: the correlation length, relaxation time, vanishing wavenumber limit (static susceptibility), the hydrodynamic regime of the pair correlation function, and the amplitude of the order parameter. The respective critical exponents agree in both setups and are given by ν⊥=1 ,ν∥=2 ,γ =1 ,η ≈0.6 -0.67 , and β =1 /2 , whereas the dynamical critical exponent is z =ν∥/ν⊥=2 . The agreement on five exponents is an exigent test for the universality of the transition. Thus, while dissipation is strictly necessary to form the crystal, the path the system undergoes toward the phase separation is part of a well-defined universality class. In fact, the local order shows critical properties while density does not. Being the later conserved, the appropriate model that couples both is model C in the Hohenberg and Halperin classification. The measured exponents are in accord with the nonequilibrium extension to model C if we assume that α , the exponent associated in equilibrium to the specific heat divergence but with no counterpart in this nonequilibrium experiment, vanishes.

  18. Development and Optimization of a Flocculation Procedure for Improved Solid-Liquid Separation of Digested Biomass

    SciTech Connect

    Patton, Caroline; Lischeske, James J.; Sievers, David A.

    2015-11-03

    One viable treatment method for conversion of lignocellulosic biomass to biofuels begins with saccharification (thermochemical pretreatment and enzymatic hydrolysis), followed by fermentation or catalytic upgrading to fuels such as ethanol, butanol, or other hydrocarbons. The post-hydrolysis slurry is typically 4-8 percent insoluble solids, predominantly consisting of lignin. Suspended solids are known to inhibit fermentation as well as poison catalysts and obstruct flow in catalyst beds. Thus a solid-liquid separation following enzymatic hydrolysis would be highly favorable for process economics, however the material is not easily separated by filtration or gravimetric methods. Use of a polyacrylamide flocculant to bind the suspended particles in a corn stover hydrolyzate slurry into larger flocs (1-2mm diameter) has been found to be extremely helpful in improving separation. Recent and ongoing research on novel pretreatment methods yields hydrolyzate material with diverse characteristics. Therefore, we need a thorough understanding of rapid and successful flocculation design in order to quickly achieve process design goals. In this study potential indicators of flocculation performance were investigated in order to develop a rapid analysis method for flocculation procedure in the context of a novel hydrolyzate material. Flocculation conditions were optimized on flocculant type and loading, pH, and mixing time. Filtration flux of the hydrolyzate slurry was improved 170-fold using a cationic polyacrylamide flocculant with a dosing of approximately 22 mg flocculant/g insoluble solids at an approximate pH of 3. With cake washing, sugar recovery exceeded 90 percent with asymptotic yield at 15 L wash water/kg insoluble solids.

  19. A Bottom-Up Approach to Understanding Protein Layer Formation at Solid-Liquid Interfaces

    PubMed Central

    Kastantin, Mark; Langdon, Blake B.; Schwartz, Daniel K.

    2014-01-01

    A common goal across different fields (e.g. separations, biosensors, biomaterials, pharmaceuticals) is to understand how protein behavior at solid-liquid interfaces is affected by environmental conditions. Temperature, pH, ionic strength, and the chemical and physical properties of the solid surface, among many factors, can control microscopic protein dynamics (e.g. adsorption, desorption, diffusion, aggregation) that contribute to macroscopic properties like time-dependent total protein surface coverage and protein structure. These relationships are typically studied through a top-down approach in which macroscopic observations are explained using analytical models that are based upon reasonable, but not universally true, simplifying assumptions about microscopic protein dynamics. Conclusions connecting microscopic dynamics to environmental factors can be heavily biased by potentially incorrect assumptions. In contrast, more complicated models avoid several of the common assumptions but require many parameters that have overlapping effects on predictions of macroscopic, average protein properties. Consequently, these models are poorly suited for the top-down approach. Because the sophistication incorporated into these models may ultimately prove essential to understanding interfacial protein behavior, this article proposes a bottom-up approach in which direct observations of microscopic protein dynamics specify parameters in complicated models, which then generate macroscopic predictions to compare with experiment. In this framework, single-molecule tracking has proven capable of making direct measurements of microscopic protein dynamics, but must be complemented by modeling to combine and extrapolate many independent microscopic observations to the macro-scale. The bottom-up approach is expected to better connect environmental factors to macroscopic protein behavior, thereby guiding rational choices that promote desirable protein behaviors. PMID:24484895

  20. Digestion of frozen/thawed food waste in the hybrid anaerobic solid-liquid system

    SciTech Connect

    Stabnikova, O. Liu, X.Y.; Wang, J.Y.

    2008-07-01

    The hybrid anaerobic solid-liquid (HASL) system, which is a modified two-phase anaerobic digester, is to be used in an industrial scale operation to minimize disposal of food waste at incineration plants in Singapore. The aim of the present research was to evaluate freezing/thawing of food waste as a pre-treatment for its anaerobic digestion in the HASL system. The hydrolytic and fermentation processes in the acidogenic reactor were enhanced when food waste was frozen for 24 h at -20 deg. C and then thawed for 12 h at 25 deg. C (experiment) in comparison with fresh food waste (control). The highest dissolved COD concentrations in the leachate from the acidogenic reactors were 16.9 g/l on day 3 in the control and 18.9 g/l on day 1 in the experiment. The highest VFA concentrations in the leachate from the acidogenic reactors were 11.7 g/l on day 3 in the control and 17.0 g/l on day 1 in the experiment. The same volume of methane was produced during 12 days in the control and 7 days in the experiment. It gave the opportunity to diminish operational time of batch process by 42%. The effect of freezing/thawing of food waste as pre-treatment for its anaerobic digestion in the HASL system was comparable with that of thermal pre-treatment of food waste at 150 deg. C for 1 h. However, estimation of energy required either to heat the suspended food waste to 150 deg. C or to freeze the same quantity of food waste to -20 deg. C showed that freezing pre-treatment consumes about 3 times less energy than thermal pre-treatment.

  1. The Interaction Between an Insoluble Particle and an Advancing Solid/Liquid Interface: Micro-Gravity Experiments and Theoretical Developments

    NASA Technical Reports Server (NTRS)

    Catalina, Adrian V.; Ssen, Subhayu; Stefanescu, Doru M.

    2003-01-01

    The interaction of an insoluble particle with an advancing solid/liquid interface (SLI) has been a subject of investigation for the past four decades. While the original interest stemmed from geology applications (e.g., frost heaving in soil), researchers soon realized that the complex science associated with such an interaction is relevant to many other scientific fields encompassing metal matrix composites (MMCs), high temperature superconductors, inclusion management in steel, growth of monotectics, and preservation of biological cells. During solidification of a liquid containing an insoluble particle, three distinct interaction phenomena have been experimentally observed: instantaneous engulfment of the particle, continuous pushing, and particle pushing followed by engulfment. It was also observed that for given experimental conditions and particle size there is a critical solidification velocity, V(sub cr), above which a particle is engulfed. During solidification of MMCs pushing leads to particle agglomeration at the grain boundaries and this has detrimental effects on mechanical properties of the casting. Consequently, the process must be designed for instantaneous engulfment to occur. This implies the development of accurate theoretical models to predict V(sub cr), and perform benchmark experiments to test the validity of such models. Although considerable progress has been made in understanding the pushing/engulfment phenomenon (PEP), its quantification in terms of the material and processing parameters remains a focus of research. Since natural convection currents occurring during terrestrial solidification experiments complicate the study of PEP, execution of experiments on the International Space Station (ISS) has been approved and funded by NASA. Extensive terrestrial (1g) experiments and preliminary micro-gravity (mu g) experiments on two space shuttle missions have been conducted in preparation for future experiments on the ISS. The investigated

  2. Development and utilization of optical low coherence reflectometry for the study of multiple scattering in randomly distributed solid-liquid suspensions

    NASA Astrophysics Data System (ADS)

    Randall, Summer Lockerbie

    The investigation of Optical Low Coherence Reflectometry (OLCR) for evaluation of highly scattering suspensions involves a balance between the observation of real systems and theoretical development. The main focus of this work was the development and utilization of OLCR to investigate highly scattering solid-liquid suspensions over a wide range of particle sizes, using monodispersed, bimodal, and polydispersed polystyrene nanosphere suspensions and Department of Energy (DOE) waste surrogates. The results were the first experimental demonstration that coherent optical backscattering from media with randomly distributed spherical nanoparticles is dominated by Mie resonances. Industrial process samples of various sizes and dispersity were also measured to expand the applicability of OLCR to a wide range of process needs. Current research has focused on the deconvolution of sample parameters from the tailing decay profiles of highly scattering matrices. Significant progress has been made on data analysis methods for monodispersed and more complex compositions of polystyrene suspensions and these methods have been applied to HLW surrogate suspensions and several industrial models. The research described within this dissertation has implications for measurement needs on basic science, industrial, and national laboratory levels. The scope of this research includes advancements in both fundamental understanding of multiple scattering through analysis of model systems and in development and application of the technology to current measurement needs within industry.

  3. Spontaneous mode-selection in the self-propelled motion of a solid/liquid composite driven by interfacial instability

    NASA Astrophysics Data System (ADS)

    Takabatake, Fumi; Magome, Nobuyuki; Ichikawa, Masatoshi; Yoshikawa, Kenichi

    2011-03-01

    Spontaneous motion of a solid/liquid composite induced by a chemical Marangoni effect, where an oil droplet attached to a solid soap is placed on a water phase, was investigated. The composite exhibits various characteristic motions, such as revolution (orbital motion) and translational motion. The results showed that the mode of this spontaneous motion switches with a change in the size of the solid scrap. The essential features of this mode-switching were reproduced by ordinary differential equations by considering nonlinear friction with proper symmetry.

  4. Bubble Induced Disruption of a Planar Solid-Liquid Interface During Controlled Directional Solidification in a Microgravity Environment

    NASA Technical Reports Server (NTRS)

    Grugel, Richard N.; Brush, Lucien N.; Anilkumar, Amrutur V.

    2013-01-01

    Pore Formation and Mobility Investigation (PFMI) experiments were conducted in the microgravity environment aboard the International Space Station with the intent of better understanding the role entrained porosity/bubbles play during controlled directional solidification. The planar interface in a slowing growing succinonitrile - 0.24 wt% water alloy was being observed when a nitrogen bubble traversed the mushy zone and remained at the solid-liquid interface. Breakdown of the interface to shallow cells subsequently occurred, and was later evaluated using down-linked data from a nearby thermocouple. These results and other detrimental effects due to the presence of bubbles during solidification processing in a microgravity environment are presented and discussed.

  5. Experimental determination and prediction of (solid+liquid) phase equilibria for binary mixtures of heavy alkanes and fatty acids

    NASA Astrophysics Data System (ADS)

    Benziane, Mokhtar; Khimeche, Kamel; Dahmani, Abdellah; Nezar, Sawsen; Trache, Djalal

    2012-06-01

    Solid-liquid equilibria for three binary mixtures, n-Eicosane (1) + Lauric acid (2), n-Tetracosane (1) + Stearic acid (2), and n-Octacosane (1) + Palmitic acid (2), were measured using a differential scanning calorimeter. Simple eutectic behaviour was observed for these systems. The experimental results were correlated by means of the modified UNIFAC (Larsen and Gmehling versions), UNIQUAC and ideal models. The root-mean-square deviations of the solubility temperatures for all measured data vary from 0.26 to 3.15 K and depend on the particular model used. The best solubility correlation was obtained with the UNIQUAC model.

  6. Biphasic Metal Films: Intrinsically Stretchable Biphasic (Solid-Liquid) Thin Metal Films (Adv. Mater. 22/2016).

    PubMed

    Hirsch, Arthur; Michaud, Hadrien O; Gerratt, Aaron P; de Mulatier, Séverine; Lacour, Stéphanie P

    2016-06-01

    On page 4507, S. P. Lacour and co-workers present highly conductive and stretchable solid-liquid films that are formed by physical vapor deposition of gallium onto an alloying gold layer. The image shows patterns defined by lift-off on an elastomer membrane. The magnified view is a false-color scanning electron microscopy (SEM) image (×5000) of the surface of the films under 50% applied strain, showing the liquid Ga (blue-gray) flowing between the AuGa2 /Ga clusters (gold). PMID:27273441

  7. In-Situ Observations of Interaction Between Particulate Agglomerates and an Advancing Planar Solid/Liquid Interface: Microgravity Experiments

    NASA Technical Reports Server (NTRS)

    Sen, S.; Juretzko, F.; Stefanescu, D. M.; Dhindaw, B. K.; Curreri, P. A.

    1999-01-01

    Results are reported of directional solidification experiments on particulate agglomerate pushing and engulfment by a planar solid/liquid (s/1) interface. These experiments were conducted on the Space Shuttle Columbia during the United States Microgravity Payload 4 (USMP-4) Mission. It was found that the pushing to engulfment transition velocity, V(sub ct),, for agglomerates depends not only on their effective size but also their orientation with respect to the s/l interface. The analytical model for predicting V(sub cr) of a single particle was subsequently enhanced to predict V(sub cr) of the agglomerates by considering their shape factor and orientation.

  8. In Situ Observations of Interaction Between Particulate Agglomerates and an Advancing Planar Solid/Liquid Interface: Microgravity Experiments

    NASA Technical Reports Server (NTRS)

    Sen, S.; Juretzko, F.; Stafanescu, D. M.; Dhindaw, B. K.; Curreri, P. A.

    1999-01-01

    Results are reported of directional solidification experiments on particulate agglomerate pushing and engulfment by a planar solid/liquid (s/l) interface. These experiments were conducted on the Space Shuttle Columbia during the United States Microgravity Payload 4 (USMP-4) Mission. It was found that the pushing to engulfment transition velocity, V(sub cr) for agglomerates depends not only on their effective size but also their orientation with respect to the s,1 interface. The analytical model for predicting V(sub cr) of a single particle was subsequently enhanced to predict V(sub cr) of the agglomerates by considering their shape factor and orientation.

  9. Numerical determination of the interfacial energy and nucleation barrier of curved solid-liquid interfaces in binary systems

    NASA Astrophysics Data System (ADS)

    Kundin, Julia; Choudhary, Muhammad Ajmal

    2016-07-01

    The phase-field crystal (PFC) technique is a widely used approach for modeling crystal growth phenomena with atomistic resolution on mesoscopic time scales. We use a two-dimensional PFC model for a binary system based on the work of Elder et al. [Phys. Rev. B 75, 064107 (2007), 10.1103/PhysRevB.75.064107] to study the effect of the curved, diffuse solid-liquid interface on the interfacial energy as well as the nucleation barrier. The calculation of the interfacial energy and the nucleation barrier certainly depends on the proper definition of the solid-liquid dividing surface and the corresponding nucleus size. We define the position of the sharp interface at which the interfacial energy is to be evaluated by using the concept of equimolar dividing surface (re) and the minimization of the interfacial energy (rs). The comparison of the results based on both radii shows that the difference re-rs is always positive and has a limit for large cluster sizes which is comparable to the Tolman length. Furthermore, we found the real nucleation barrier for small cluster sizes, which is defined as a function of the radius rs, and compared it with the classical nucleation theory. The simulation results also show that the extracted interfacial energy as function of both radii is independent of system size, and this dependence can be reasonably described by the nonclassical Tolman formula with a positive Tolman length.

  10. Numerical simulation on the performance of the vortex pump for transporting solid-liquid two-phase with light particles

    NASA Astrophysics Data System (ADS)

    Mao, W. Y.; Song, P. Y.; Deng, Q. G.; Xu, H. J.

    2016-05-01

    With the purpose of studying performance of the vortex pump for transporting solid-liquid two-phase with light particles whose relative density smaller than 1, the numerical simulation of solid-liquid two phase flowing in the whole channel of a vortex pump with the particle diameter being 0.5 mm, 1 mm, 2 mm, 3 mm and the initial solid phase volume concentrations being 10%, 20% and 30% are respectively carried out by using the commercial software ANSYS Fluent by adopting RNG κ-ɛ turbulent flow model, Eulerian-Eulerian multi-phase flow model and SIMPLEC algorithm. The simulation results show that in the impeller region, the particles concentrate on the non-working surface of the blades, and the particles are rare on the working surface of the blades. As the initial solid phase volume concentration and particle diameter increase, the pump delivery head of vortex pump decrease. The pump delivery head of vortex pump with different initial solid phase concentrations and different particle diameters are predicted and compared with those obtained by an empirical formula, and they shows good agreement.

  11. Total enthalpy-based lattice Boltzmann method with adaptive mesh refinement for solid-liquid phase change

    NASA Astrophysics Data System (ADS)

    Huang, Rongzong; Wu, Huiying

    2016-06-01

    A total enthalpy-based lattice Boltzmann (LB) method with adaptive mesh refinement (AMR) is developed in this paper to efficiently simulate solid-liquid phase change problem where variables vary significantly near the phase interface and thus finer grid is required. For the total enthalpy-based LB method, the velocity field is solved by an incompressible LB model with multiple-relaxation-time (MRT) collision scheme, and the temperature field is solved by a total enthalpy-based MRT LB model with the phase interface effects considered and the deviation term eliminated. With a kinetic assumption that the density distribution function for solid phase is at equilibrium state, a volumetric LB scheme is proposed to accurately realize the nonslip velocity condition on the diffusive phase interface and in the solid phase. As compared with the previous schemes, this scheme can avoid nonphysical flow in the solid phase. As for the AMR approach, it is developed based on multiblock grids. An indicator function is introduced to control the adaptive generation of multiblock grids, which can guarantee the existence of overlap area between adjacent blocks for information exchange. Since MRT collision schemes are used, the information exchange is directly carried out in the moment space. Numerical tests are firstly performed to validate the strict satisfaction of the nonslip velocity condition, and then melting problems in a square cavity with different Prandtl numbers and Rayleigh numbers are simulated, which demonstrate that the present method can handle solid-liquid phase change problem with high efficiency and accuracy.

  12. Interaction of SiC particles with moving solid-liquid interface during directional solidification of silicon

    NASA Astrophysics Data System (ADS)

    Friedrich, J.; Reimann, C.; Jauss, T.; Cröll, A.; Sorgenfrei, T.

    2016-08-01

    In this work, the interaction of SiC particles, having sizes of 7 μm to 300 μm, with the moving solid-liquid interface during directional solidification of silicon was experimentally and theoretically investigated. This included both convective and nearly diffusive conditions. In the nearly diffusive regime under microgravity, the particles were incorporated at a lower growth velocity than in the convective regime under 1g conditions. The experimental data were compared to simple theoretical models allowing the calculation of the critical growth velocity for the incorporation of spherical particles in dependence of the particle size. It was found that the theoretical results could qualitatively explain the experimental observations when a proper set of equations for the forces acting on the particle and of the material constants are chosen. It can be concluded that sedimentation of the particles due to gravity seems to play a role only for large particles. On the other hand, melt flow might cause a lift force which would push the particles away from the solid-liquid interface, and thus would result in higher critical growth velocities under convective conditions, e.g. due to buoyancy convection. Therefore, a contribution of the missing lift force under μg conditions could lead to the smaller critical growth velocity for particle incorporation that is observed under microgravity.

  13. Fast contact of solid-liquid interface created high strength multi-layered cellulose hydrogels with controllable size.

    PubMed

    He, Meng; Zhao, Yanteng; Duan, Jiangjiang; Wang, Zhenggang; Chen, Yun; Zhang, Lina

    2014-02-12

    Novel onion-like and multi-layered tubular cellulose hydrogels were constructed, for the first time, from the cellulose solution in a 7% NaOH/12% urea aqueous solvent by changing the shape of the gel cores. In our findings, the contacting of the cellulose solution with the surface of the agarose gel rod or sphere loaded with acetic acid led to the close chain packing to form immediately a gel layer, as a result of the destruction of the cellulose inclusion complex by acid through inducing the cellulose self-aggregation. Subsequently, multi-layered cellulose hydrogels were fabricated via a multi-step interrupted gelation process. The size, layer thickness and inter-layer space of the multi-layered hydrogels could be controlled by adjusting the cellulose concentrations, the gel core diameter and the contacting time of the solid-liquid interface. The multi-layered cellulose hydrogels displayed good architectural stability and solvent resistance. Moreover, the hydrogels exhibited high compressive strength and excellent biocompatibility. L929 cells could adhere and proliferate on the surface of the layers and in interior space, showing great potential as tissue engineering scaffolds and cell culture carrier. This work opens up a new avenue for the construction of the high strength multi-layered cellulose hydrogels formed from inner to outside via a fast contact of solid-liquid interface. PMID:24405277

  14. Transformation of ferulic acid to vanillin using a fed-batch solid-liquid two-phase partitioning bioreactor.

    PubMed

    Ma, Xiao-kui; Daugulis, Andrew J

    2014-01-01

    Amycolatopsis sp. ATCC 39116 (formerly Streptomyces setonii) has shown promising results in converting ferulic acid (trans-4-hydroxy-3-methoxycinnamic acid; substrate), which can be derived from natural plant wastes, to vanillin (4-hydroxy-3-methoxybenzaldehyde). After exploring the influence of adding vanillin at different times during the growth cycle on cell growth and transformation performance of this strain and demonstrating the inhibitory effect of vanillin, a solid-liquid two-phase partitioning bioreactor (TPPB) system was used as an in situ product removal technique to enhance transformation productivity by this strain. The thermoplastic polymer Hytrel(®) G4078W was found to have superior partitioning capacity for vanillin with a partition coefficient of 12 and a low affinity for the substrate. A 3-L working volume solid-liquid fed-batch TPPB mode, using 300 g Hytrel G4078W as the sequestering phase, produced a final vanillin concentration of 19.5 g/L. The overall productivity of this reactor system was 450 mg/L. h, among the highest reported in literature. Vanillin was easily and quantitatively recovered from the polymers mostly by single stage extraction into methanol or other organic solvents used in food industry, simultaneously regenerating polymer beads for reuse. A polymer-liquid two phase bioreactor was again confirmed to easily outperform single phase systems that feature inhibitory or easily further degraded substrates/products. This enhancement strategy might reasonably be expected in the production of other flavor and fragrance compounds obtained by biotransformations. PMID:24167066

  15. Janus Solid-Liquid Interface Enabling Ultrahigh Charging and Discharging Rate for Advanced Lithium-Ion Batteries.

    PubMed

    Zheng, Jiaxin; Hou, Yuyang; Duan, Yandong; Song, Xiaohe; Wei, Yi; Liu, Tongchao; Hu, Jiangtao; Guo, Hua; Zhuo, Zengqing; Liu, Lili; Chang, Zheng; Wang, Xiaowei; Zherebetskyy, Danylo; Fang, Yanyan; Lin, Yuan; Xu, Kang; Wang, Lin-Wang; Wu, Yuping; Pan, Feng

    2015-09-01

    LiFePO4 has long been held as one of the most promising battery cathode for its high energy storage capacity. Meanwhile, although extensive studies have been conducted on the interfacial chemistries in Li-ion batteries,1-3 little is known on the atomic level about the solid-liquid interface of LiFePO4/electrolyte. Here, we report battery cathode consisted with nanosized LiFePO4 particles in aqueous electrolyte with an high charging and discharging rate of 600 C (3600/600 = 6 s charge time, 1 C = 170 mAh g(-1)) reaching 72 mAh g(-1) energy storage (42% of the theoretical capacity). By contrast, the accessible capacity sharply decreases to 20 mAh g(-1) at 200 C in organic electrolyte. After a comprehensive electrochemistry tests and ab initio calculations of the LiFePO4-H2O and LiFePO4-EC (ethylene carbonate) systems, we identified the transient formation of a Janus hydrated interface in the LiFePO4-H2O system, where the truncated symmetry of solid LiFePO4 surface is compensated by the chemisorbed H2O molecules, forming a half-solid (LiFePO4) and half-liquid (H2O) amphiphilic coordination environment that eases the Li desolvation process near the surface, which makes a fast Li-ion transport across the solid/liquid interfaces possible. PMID:26305572

  16. Inferences about radionuclide mobility in soils based on the solid/liquid partition coefficients and soil properties.

    PubMed

    Sohlenius, Gustav; Saetre, Peter; Nordén, Sara; Grolander, Sara; Sheppard, Steve

    2013-05-01

    To assist transport modeling in assessments of the radiological impact of a geological repository for radioactive wastes, the mobility of various elements was studied in arable and wetland soils in the Forsmark region, Sweden. Pore water and total element contents were determined for five types of unconsolidated deposits (regolith), spanning a wide range of soil properties with respect to pH and organic matter content. Two soil depths were sampled to capture element mobility in regolith layers affected and unaffected by soil-forming processes. The solid/liquid partition coefficients (K d values) for most elements varied significantly among regolith types. For most elements, the observed variations in K d values could be explained by variations in soil properties. For many elements, mobility increased with decreasing soil pH. The results provide a significant addition of data on radionuclide retention in soils, taking account of soil properties and processes. PMID:23619799

  17. The use of hard- and soft-modelling to predict radiostrontium solid-liquid distribution coefficients in soils.

    PubMed

    Gil-García, C J; Rigol, A; Vidal, M

    2011-11-01

    The solid-liquid distribution coefficient (K(d)) is the parameter that governs the incorporation of contaminants in soils. Its estimation allows the prediction of the fate of contaminants in the short- and long-term after a contamination event. Here, the K(d) of radiostrontium (K(d)(Sr)), a radionuclide of significant environmental interest, was predicted by hard models, which are based on knowledge of the mechanisms governing its sorption, and by soft models based on Partial Least Squares (PLS), using a large data set with the main soil parameters. The two approaches were tested and compared for 30 soils in Spain. Correlations between the predicted and experimental values of K(d)(Sr) obtained using hard- and soft-modelling showed slopes close to 1 and regression coefficients higher than 0.95, which confirms that both approaches are able to obtain satisfactory estimates for K(d)(Sr) from soil parameters. PMID:21890173

  18. Three-dimensional atomic force microscopy mapping at the solid-liquid interface with fast and flexible data acquisition

    NASA Astrophysics Data System (ADS)

    Söngen, Hagen; Nalbach, Martin; Adam, Holger; Kühnle, Angelika

    2016-06-01

    We present the implementation of a three-dimensional mapping routine for probing solid-liquid interfaces using frequency modulation atomic force microscopy. Our implementation enables fast and flexible data acquisition of up to 20 channels simultaneously. The acquired data can be directly synchronized with commercial atomic force microscope controllers, making our routine easily extendable for related techniques that require additional data channels, e.g., Kelvin probe force microscopy. Moreover, the closest approach of the tip to the sample is limited by a user-defined threshold, providing the possibility to prevent potential damage to the tip. The performance of our setup is demonstrated by visualizing the hydration structure above the calcite (10.4) surface in water.

  19. Growing TiO2 nanowires by solid-liquid-solid mechanism including two factors (Ti and O)

    NASA Astrophysics Data System (ADS)

    Pishekloo, S. Piri; Dariani, R. S.

    2016-04-01

    Identifying the growth factors of nanowires helps in controlling their structure and morphology and determining their optimal growth conditions. This study investigates the effect of titanium substrate in growing TiO2 nanowires (NWs) with evaporation method. It reveals that the titanium in substrate is indeed the main source of growth. Using the substrate as the only source of growth with regulated amount of accessible oxygen in the furnace, NWs with lengths ranging from 1 to 70 µm were obtained. The results of the experiments show that the nanowires' growth is mainly controlled by diffusion of titanium atoms from the substrate through TiO2 grain boundaries and surface diffusion toward NWs' tips rather than adsorption from vapor phase. The solid-liquid-solid mechanism including two factors (Ti and O) is proposed and discussed for growth of TiO2 NWs.

  20. Calculating the role of composition in the anisotropy of solid-liquid interface energy using phase-field-crystal theory

    NASA Astrophysics Data System (ADS)

    Jugdutt, Bernadine A.; Ofori-Opoku, Nana; Provatas, Nikolas

    2015-10-01

    This work uses Ginzburg-Landau theory derived from a recent structural phase-field-crystal model of binary alloys developed by the authors to study the roles of concentration, temperature, and pressure on the interfacial energy anisotropy of a solid-liquid front. It is found that the main contribution to the change in anisotropy with concentration arises from a change in preferred crystallographic orientation controlled by solute-dependent changes in the two-point density correlation function of a binary alloy, a mechanism that leads to such phenomena as solute-induced elastic strain and dislocation-assisted solute clustering. Our results are consistent with experimental observations in recent studies by Rappaz et al. [J. Fife, P. Di Napoli, and M. Rappaz, Metall. Mater. Trans. A 44, 5522 (2013), 10.1007/s11661-013-1912-7]. This is the first PFC work, to our knowledge, to incorporate temperature, pressure, and density into the thermodynamic description of alloys.

  1. Crystal growth kinetics in Lennard-Jones and Weeks-Chandler-Andersen systems along the solid-liquid coexistence line

    NASA Astrophysics Data System (ADS)

    Benjamin, Ronald; Horbach, Jürgen

    2015-07-01

    Kinetics of crystal-growth is investigated along the solid-liquid coexistence line for the (100), (110), and (111) orientations of the Lennard-Jones (LJ) and Weeks-Chandler-Andersen (WCA) fcc crystal-liquid interface, using non-equilibrium molecular dynamics simulations. A slowing down of the growth kinetics along the coexistence line is observed, which is due to the decrease of the melting enthalpy with increasing coexistence temperature and pressure. Other quantities such as the melting pressure and liquid self-diffusion coefficient have a comparatively lesser impact on the kinetic growth coefficient. Growth kinetics of the LJ and WCA potentials become similar at large values of the melting temperature and pressure, when both resemble a purely repulsive soft-sphere potential. Classical models of crystallization from the melt are in reasonable qualitative agreement with our simulation data. Finally, several one-phase empirical melting/freezing rules are studied with respect to their validity along the coexistence line.

  2. Calculating the role of composition in the anisotropy of solid-liquid interface energy using phase-field-crystal theory.

    PubMed

    Jugdutt, Bernadine A; Ofori-Opoku, Nana; Provatas, Nikolas

    2015-10-01

    This work uses Ginzburg-Landau theory derived from a recent structural phase-field-crystal model of binary alloys developed by the authors to study the roles of concentration, temperature, and pressure on the interfacial energy anisotropy of a solid-liquid front. It is found that the main contribution to the change in anisotropy with concentration arises from a change in preferred crystallographic orientation controlled by solute-dependent changes in the two-point density correlation function of a binary alloy, a mechanism that leads to such phenomena as solute-induced elastic strain and dislocation-assisted solute clustering. Our results are consistent with experimental observations in recent studies by Rappaz et al. [J. Fife, P. Di Napoli, and M. Rappaz, Metall. Mater. Trans. A 44, 5522 (2013)]. This is the first PFC work, to our knowledge, to incorporate temperature, pressure, and density into the thermodynamic description of alloys. PMID:26565255

  3. Dynamic formation of a solid-liquid electrolyte interphase and its consequences for hybrid-battery concepts.

    PubMed

    Busche, Martin R; Drossel, Thomas; Leichtweiss, Thomas; Weber, Dominik A; Falk, Mareike; Schneider, Meike; Reich, Maria-Louisa; Sommer, Heino; Adelhelm, Philipp; Janek, Jürgen

    2016-05-01

    The discharging and charging of batteries require ion transfer across phase boundaries. In conventional lithium-ion batteries, Li(+) ions have to cross the liquid electrolyte and only need to pass the electrode interfaces. Future high-energy batteries may need to work as hybrids, and so serially combine a liquid electrolyte and a solid electrolyte to suppress unwanted redox shuttles. This adds new interfaces that might significantly decrease the cycling-rate capability. Here we show that the interface between a typical fast-ion-conducting solid electrolyte and a conventional liquid electrolyte is chemically unstable and forms a resistive solid-liquid electrolyte interphase (SLEI). Insights into the kinetics of this new type of interphase are obtained by impedance studies of a two-chamber cell. The chemistry of the SLEI, its growth with time and the influence of water impurities are examined by state-of-the-art surface analysis and depth profiling. PMID:27102676

  4. Dynamic formation of a solid-liquid electrolyte interphase and its consequences for hybrid-battery concepts

    NASA Astrophysics Data System (ADS)

    Busche, Martin R.; Drossel, Thomas; Leichtweiss, Thomas; Weber, Dominik A.; Falk, Mareike; Schneider, Meike; Reich, Maria-Louisa; Sommer, Heino; Adelhelm, Philipp; Janek, Jürgen

    2016-05-01

    The discharging and charging of batteries require ion transfer across phase boundaries. In conventional lithium-ion batteries, Li+ ions have to cross the liquid electrolyte and only need to pass the electrode interfaces. Future high-energy batteries may need to work as hybrids, and so serially combine a liquid electrolyte and a solid electrolyte to suppress unwanted redox shuttles. This adds new interfaces that might significantly decrease the cycling-rate capability. Here we show that the interface between a typical fast-ion-conducting solid electrolyte and a conventional liquid electrolyte is chemically unstable and forms a resistive solid-liquid electrolyte interphase (SLEI). Insights into the kinetics of this new type of interphase are obtained by impedance studies of a two-chamber cell. The chemistry of the SLEI, its growth with time and the influence of water impurities are examined by state-of-the-art surface analysis and depth profiling.

  5. Free-Surface Optical Scattering as an Indicator of the Shock-Induced Solid-Liquid Phase Transition in Tin

    SciTech Connect

    Stevens, G. D.; Lutz, S. S.; Marshall, B. R.; Turley, W. D.; Veeser, L. R.; Furlanetto, M. R.; Hixson, R. S.; Holtkamp, D. B.; Jensen, B. J.; Rigg, P. A.; Wilke, M. D.

    2008-07-01

    When highly polished metal surfaces melt upon release after shock loading, they exhibit features that suggest significant surface changes accompany the phase transition. The reflection of light from such surfaces changes from specular (pre-shock) to diffuse upon melting. A familiar manifestation of this phenomenon is the loss of signal light in VISAR measurements, which occurs at pressures high enough to melt the free surface. Unlike many other potential material phase-sensitive diagnostics (e.g., reflectometry, conductivity) that show relatively small (1%–10%) changes, the specularity of reflection provides a more sensitive and definitive indication of the solid-liquid phase transition. Data will be presented that support the hypothesis that specularity changes indicate melt in a way that can be measured easily and unambiguously.

  6. Resonant anomalous x-ray reflectivity as a probe of ion adsorption at solid-liquid interfaces.

    SciTech Connect

    Fenter, P.; Park, C.; Nagy, K. L.; Sturchio, N. C.; Chemistry; Univ. of Illinois at Chicago

    2007-05-23

    We discuss new opportunities to understand processes at the solid-liquid interface using resonant anomalous X-ray reflectivity (RAXR). This approach is illustrated by determination of element-specific density profiles at mica surfaces in aqueous electrolyte solutions containing Rb{sup +} and Sr{sup 2+}. The total interfacial electron density profile is determined by specular reflectivity (i.e., reflected intensity vs. momentum transfer, q, at an energy, E, far from any characteristic absorption edge). RAXR spectra (i.e., intensity vs. E at fixed q) reveal element-specific ion distributions. Key differences in the interaction of Rb{sup +} and Sr{sup 2+} with mica are observed using resonant anomalous X-ray reflectivity: Rb{sup +} adsorbs in a partially hydrated state, but Sr{sup 2+} adsorbs in both fully and partially hydrated states.

  7. Solid-liquid-solid process for forming free-standing gold nanowhisker superlattice by interfering femtosecond laser irradiation

    NASA Astrophysics Data System (ADS)

    Nakata, Y.; Miyanaga, N.; Momoo, K.; Hiromoto, T.

    2013-06-01

    One-dimensional nanomaterial superlattices are fundamental components in plasmonics, nanophotonics, and nanoelectronics. Bottom-up techniques such as vapour-liquid-solid (VLS) and chemosynthesis have been used to fabricate the structure but are nonoptimal for controlling alignment and size. Here we report the fabrication of gold nanowhisker superlattice, based on a novel mechanism termed solid-liquid-solid (SLS). An interfering femtosecond laser pulse induces fluid flows of nanosize gold, which is followed by droplets pinching off from them and freezing of a free-standing nanowhisker superlattice fixed on a substrate. The shape is defined by liquid motion and not by crystallographic growth although its structure is polycrystalline. The smallest curvature radius of its vertex was 3.4 nm, which is one-half of the smallest nanorods fabricated by chemosynthesis. SLS process is a superior alternative to sequential bottom-up processes involving catalyst fabrication, bottom-up synthesis, purification, alignment, stabilization, and preservation.

  8. Detection of different oxidation states of individual manganese porphyrins during their reaction with oxygen at a solid/liquid interface

    NASA Astrophysics Data System (ADS)

    den Boer, Duncan; Li, Min; Habets, Thomas; Iavicoli, Patrizia; Rowan, Alan E.; Nolte, Roeland J. M.; Speller, Sylvia; Amabilino, David B.; de Feyter, Steven; Elemans, Johannes A. A. W.

    2013-07-01

    Manganese porphyrins have been extensively investigated as model systems for the natural enzyme cytochrome P450 and as synthetic oxidation catalysts. Here, we report single-molecule studies of the multistep reaction of manganese porphyrins with molecular oxygen at a solid/liquid interface, using a scanning tunnelling microscope (STM) under environmental control. The high lateral resolution of the STM, in combination with its sensitivity to subtle differences in the electronic properties of molecules, allowed the detection of at least four distinct reaction species. Real-space and real-time imaging of reaction dynamics enabled the observation of active sites, immobile on the experimental timescale. Conversions between the different species could be tuned by the composition of the atmosphere (argon, air or oxygen) and the surface bias voltage. By means of extensive comparison of the results to those obtained by analogous solution-based chemistry, we assigned the observed species to the starting compound, reaction intermediates and products.

  9. Solid-liquid boundaries in iron-rich alloys and the age of the Earth's inner core

    NASA Astrophysics Data System (ADS)

    Li, J.; Chen, B.; Gao, L.

    2006-05-01

    Melting and solidification cause major chemical differentiation in the Earth. As the Earth cools, the liquid core solidifies from the center and the inner core grows at the expense of the outer core. The timing of the onset of core solidification remains poorly constrained. Labrosse et al. (2001) estimated the age of the Earth's inner core based on energy budget considerations. In their analysis, the latent heat and gravitational energy are calculated according to dislocation melting theory. We have conducted melting experiments on pure iron and an iron-sulfur alloy containing 15 at.% sulfur, in order to determine the effect of pressure on the Clapeyron slopes of the solid-liquid boundaries. Our results allow a critical examination of the energy estimates, hence the age of the inner core. The implications for the budget of radioactive elements will be discussed.

  10. Rapid Carbonation for Calcite from a Solid-Liquid-Gas System with an Imidazolium-Based Ionic Liquid

    PubMed Central

    Ibrahim, Abdul-Rauf; Vuningoma, Jean Bosco; Huang, Yan; Wang, Hongtao; Li, Jun

    2014-01-01

    Aqueous carbonation of Ca(OH)2 is a complex process that produces calcite with scalenohedral calcite phases and characterized by inadequate carbonate species for effective carbonation due to the poor dissolution of CO2 in water. Consequently, we report a solid-liquid-gas carbonation system with an ionic liquid (IL), 1-butyl-3-methylimidazolium bromide, in view of enhancing the reaction of CO2 with Ca(OH)2. The use of the IL increased the solubility of CO2 in the aqueous environment and enhanced the transport of the reactive species (Ca2+ and CO32−) and products. The presence of the IL also avoided the formation of the CaCO3 protective and passivation layer and ensured high carbonation yields, as well as the production of stoichiometric rhombohedral calcite phases in a short time. PMID:24968273

  11. L'Anse Aux Meadows, Newfoundland

    NASA Technical Reports Server (NTRS)

    2008-01-01

    L'Anse aux Meadows is a site on the northernmost tip of the island of Newfoundland, located in the Province of Newfoundland and Labrador, Canada, where the remains of a Viking village were discovered in 1960 by the Norwegians Helge and Anne Ingstad. The only authenticated Viking settlement in North America outside Greenland, it was the site of a multi-year archaeological dig that found dwellings, tools and implements that verified its time frame. The settlement, dating more than five hundred years before Christopher Columbus, contains the earliest European structures in North America. Named a World Heritage site by UNESCO, it is thought by many to be the semi-legendary 'Vinland' settlement of explorer Leif Ericson around AD 1000. The settlement at L'Anse aux Meadows consisted of at least eight buildings, including a forge and smelter, and a lumber yard that supported a shipyard. The largest house measured 28.8 by 15.6 m and consisted of several rooms. Sewing and knitting tools found at the site indicate women were present at L'Anse aux Meadows

    The image was acquired on September 14, 2007, covers an area of 14.2 x 14.6 km, and is located at 51.5 degrees north latitude, 55.6 degrees west longitude.

    The U.S. science team is located at NASA's Jet Propulsion Laboratory, Pasadena, Calif. The Terra mission is part of NASA's Science Mission Directorate.

  12. Real-time observation of the solid-liquid-vapor dissolution of individual tin(IV) oxide nanowires.

    PubMed

    Hudak, Bethany M; Chang, Yao-Jen; Yu, Lei; Li, Guohua; Edwards, Danielle N; Guiton, Beth S

    2014-06-24

    The well-known vapor-liquid-solid (VLS) mechanism results in high-purity, single-crystalline wires with few defects and controllable diameters, and is the method of choice for the growth of nanowires for a vast array of nanoelectronic devices. It is of utmost importance, therefore, to understand how such wires interact with metallic interconnects-an understanding which relies on comprehensive knowledge of the initial growth process, in which a crystalline wire is ejected from a metallic particle. Though ubiquitous, even in the case of single elemental nanowires the VLS mechanism is complicated by competing processes at multiple heterogeneous interfaces, and despite decades of study, there are still aspects of the mechanism which are not well understood. Recent breakthroughs in studying the mechanism and kinetics of VLS growth have been strongly aided by the use of in situ techniques, and would have been impossible through other means. As well as several systematic studies of nanowire growth, reports which focus on the role and the nature of the catalyst tip reveal that the stability of the droplet is a crucial factor in determining nanowire morphology and crystallinity. Additionally, a reverse of the VLS process dubbed solid-liquid-vapor (SLV) has been found to result in the formation of cavities, or "negative nanowires". Here, we present a series of heating studies conducted in situ in the transmission electron microscope (TEM), in which we observe the complete dissolution of metal oxide nanowires into the metal catalyst particles at their tips. We are able to consistently explain our observations using a solid-liquid-vapor (SLV) type mechanism in which both evaporation at the liquid-vapor interface and adhesion of the catalyst droplet to the substrate surface contribute to the overall rate. PMID:24818706

  13. Numerical determination of the interfacial energy and nucleation barrier of curved solid-liquid interfaces in binary systems.

    PubMed

    Kundin, Julia; Choudhary, Muhammad Ajmal

    2016-07-01

    The phase-field crystal (PFC) technique is a widely used approach for modeling crystal growth phenomena with atomistic resolution on mesoscopic time scales. We use a two-dimensional PFC model for a binary system based on the work of Elder et al. [Phys. Rev. B 75, 064107 (2007)PRBMDO1098-012110.1103/PhysRevB.75.064107] to study the effect of the curved, diffuse solid-liquid interface on the interfacial energy as well as the nucleation barrier. The calculation of the interfacial energy and the nucleation barrier certainly depends on the proper definition of the solid-liquid dividing surface and the corresponding nucleus size. We define the position of the sharp interface at which the interfacial energy is to be evaluated by using the concept of equimolar dividing surface (r^{e}) and the minimization of the interfacial energy (r^{s}). The comparison of the results based on both radii shows that the difference r^{e}-r^{s} is always positive and has a limit for large cluster sizes which is comparable to the Tolman length. Furthermore, we found the real nucleation barrier for small cluster sizes, which is defined as a function of the radius r^{s}, and compared it with the classical nucleation theory. The simulation results also show that the extracted interfacial energy as function of both radii is independent of system size, and this dependence can be reasonably described by the nonclassical Tolman formula with a positive Tolman length. PMID:27575196

  14. Effect of graphene layer thickness and mechanical compliance on interfacial heat flow and thermal conduction in solid-liquid phase change materials.

    PubMed

    Warzoha, Ronald J; Fleischer, Amy S

    2014-08-13

    Solid-liquid phase change materials (PCMs) are attractive candidates for thermal energy storage and electronics cooling applications but have limited applicability in state-of-the-art technologies due to their low intrinsic thermal conductivities. Recent efforts to incorporate graphene and multilayer graphene into PCMs have led to the development of thermal energy storage materials with remarkable values of bulk thermal conductivity. However, the full potential of graphene as a filler material for the thermal enhancement of PCMs remains unrealized, largely due to an incomplete understanding of the physical mechanisms that govern thermal transport within graphene-based nanocomposites. In this work, we show that the number of graphene layers (n) within an individual graphene nanoparticle has a significant effect on the bulk thermal conductivity of an organic PCM. Results indicate that the bulk thermal conductivity of PCMs can be tuned by over an order of magnitude simply by adjusting the number of graphene layers (n) from n = 3 to 44. Using scanning electron microscopy in tandem with nanoscale analytical techniques, the physical mechanisms that govern heat flow within a graphene nanocomposite PCM are found to be nearly independent of the intrinsic thermal conductivity of the graphene nanoparticle itself and are instead found to be dependent on the mechanical compliance of the graphene nanoparticles. These findings are critical for the design and development of PCMs that are capable of cooling next-generation electronics and storing heat effectively in medium-to-large-scale energy systems, including solar-thermal power plants and building heating and cooling systems. PMID:24983698

  15. Pre-Service Primary Science Teachers' Understandings of the Effect of Temperature and Pressure on Solid-Liquid Phase Transition of Water

    ERIC Educational Resources Information Center

    Yalcin, Fatma Aggul

    2012-01-01

    The aim of this study was to explore pre-service primary teachers' understandings of the effect of temperature and pressure on the solid-liquid phase transition of water. In the study a survey approach was used, and the sample consisted of one-hundred and three, third year pre-service primary science teachers. As a tool for data collection, a test…

  16. USDA-ARS research update: Improved solid-liquid separation using polymers in flushing systems and new technology to recover the ammonia from covered lagoons

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Part 1: Improved method for recovery of organic solids from diluted swine manure: Solid-liquid separation of the raw manure increases the capacity of decision making and opportunities for treatment. The high-rate separation up-front using flocculants allows recovery of most of the organic compounds,...

  17. Surface composition variation and high-vacuum performance of DLC/ILs solid-liquid lubricating coatings: Influence of space irradiation

    NASA Astrophysics Data System (ADS)

    Liu, Xiufang; Wang, Liping; Pu, Jibin; Xue, Qunji

    2012-08-01

    In this paper, we fabricated a DLC/ionic liquid (DLC/ILs) solid-liquid lubricating coating and investigated the effect of atomic oxygen (AO), ultraviolet (UV), proton and electron irradiations on composition, structure, morphology and tribological properties of the DLC/ILs solid-liquid lubricating coatings. A ground-based simulation facility was employed to carry out the irradiation experiments. X-ray photoelectron spectroscope (XPS), Raman spectra, and Fourier Transform Infrared Spectroscopy (FTIR) were used to analyzed the structure and composition changes of DLC film and IL lubricant before and after irradiations. The tribological behavior of the DLC/ILs solid-liquid lubricating coating before and after irradiations was investigated by a vacuum tribometer with the pressure of 10-5 Pa. The experimental results revealed that irradiations induced the structural changes, including oxidation, bond break and crosslinking reactions of DLC film and IL lubricant. The damage of proton and AO irradiations to lubricating materials were the most serious, and UV irradiation was the slightest. After irradiations, the friction coefficient of the solid-liquid lubricating coatings decreased (except for AO irradiation), but the disc wear rate increased compared with non-irradiation coatings.

  18. SOLID-LIQUID PHASE TRANSFER CATALYZED SYNTHESIS OF CINNAMYL ACETATE-KINETICS AND ANALYSIS OF FACTORS AFFECTING THE REACTION IN A BATCH REACTOR

    EPA Science Inventory

    The use of solid-liquid phase transfer catalysis has an advantage of carrying out reaction between two immiscible substrates, one in solid phase and the other in liquid phase, with high selectivity and at relatively low temperatures. In this study we investigated the synthesis ci...

  19. Solid-liquid phase coexistence of alkali nitrates from molecular dynamics simulations.

    SciTech Connect

    Jayaraman, Saivenkataraman

    2010-03-01

    Alkali nitrate eutectic mixtures are finding application as industrial heat transfer fluids in concentrated solar power generation systems. An important property for such applications is the melting point, or phase coexistence temperature. We have computed melting points for lithium, sodium and potassium nitrate from molecular dynamics simulations using a recently developed method, which uses thermodynamic integration to compute the free energy difference between the solid and liquid phases. The computed melting point for NaNO3 was within 15K of its experimental value, while for LiNO3 and KNO3, the computed melting points were within 100K of the experimental values [4]. We are currently extending the approach to calculate melting temperatures for binary mixtures of lithium and sodium nitrate.

  20. Communication: Thermal rectification in liquids by manipulating the solid-liquid interface.

    PubMed

    Murad, Sohail; Puri, Ishwar K

    2012-08-28

    Thermal rectification, the origin of which lies in modifying the thermal resistance in a nonlinear manner, could significantly improve the thermal management of a wide range of nano-devices (both electronic and thermoelectric), thereby improving their efficiencies. Since rectification requires a material to be inhomogeneous, it has been typically associated with solids. However, the structure of solids is relatively difficult to manipulate, which makes the tuning of thermal rectification devices challenging. Since liquids are more amenable to tuning, this could open up new applications for thermal rectification. We use molecular dynamics simulations to demonstrate thermal rectification using liquid water. This is accomplished by creating an inhomogeneous water phase, either by changing the morphology of the surface in contact with the liquid or by imposing an arbitrary external force, which in practice could be through an electric or magnetic field. Our system consists of a bulk fluid that is confined in a reservoir that is bounded by two walls, one hot and the other cold. The interfacial (Kapitza) thermal resistance at the solid-fluid interface and the density gradient of the bulk fluid both influence the magnitude of the thermal rectification. However, we find that the role of the interfacial resistance is more prominent than the application of an external force on the bulk fluid. PMID:22938211

  1. Collaborateurs aux lignes directrices en soins primaires

    PubMed Central

    Allan, G. Michael; Kraut, Roni; Crawshay, Aven; Korownyk, Christina; Vandermeer, Ben; Kolber, Michael R.

    2015-01-01

    Résumé Objectif Déterminer la profession des collaborateurs scientifiques aux lignes directrices, les variables associées aux différences de participation des collaborateurs et si oui ou non les lignes directrices en soins primaires fournissent un énoncé sur les conflits d’intérêts. Type d’étude Analyse rétrospective des lignes directrices en soins primaires affichées sur le site web de l’Association médicale canadienne. Deux extracteurs de données indépendants ont examiné les lignes directrices et ont extrait les données pertinentes. Contexte Canada Principaux paramètres à l’étude Commanditaires des lignes directrices, territoire (national ou provincial) visé par les lignes directrices, profession des collaborateurs scientifiques aux lignes directrices et énoncés de conflits d’intérêts rapportés dans les lignes directrices. Résultats Sur les 296 lignes directrices de pratique clinique trouvées dans la section de la médecine familiale de l’Infobanque AMC, 65 apparaissaient en double et 35 se rapportaient de façon limitée à la médecine familiale. Vingt ne fournissaient aucune information sur les collaborateurs scientifiques, ce qui laissait 176 lignes directrices propices à l’analyse. Au total, il y avait 2495 collaborateurs (auteurs et membres de comité) : 1343 (53,8 %) spécialistes autres que des médecins de famille, 423 (17,0 %) médecins de famille, 141 (5,7 %) infirmières, 75 (3,0 %) pharmaciens, 269 (10,8 %) autres cliniciens, 203 (8,1 %) scientifiques non cliniciens et 41 (1,6 %) collaborateurs de profession inconnue. La proportion des collaborateurs de ces professions différait significativement entre les lignes directrices nationales et provinciales, de même qu’entre les lignes directrices financées par l’industrie et celles qui ne l’étaient pas (p < 0,001 dans les 2 cas). Dans le cas des lignes directrices de pratique clinique provinciales, 30,8 % des collaborateurs étaient des médecins de

  2. Direct imaging of complex nano- to microscale interfaces involving solid, liquid, and gas phases.

    PubMed

    Rykaczewski, Konrad; Landin, Trevan; Walker, Marlon L; Scott, John Henry J; Varanasi, Kripa K

    2012-10-23

    Surfaces with special wetting properties not only can efficiently repel or attract liquids such as water and oils but also can prevent formation of biofilms, ice, and clathrate hydrates. Predicting the wetting properties of these special surfaces requires detailed knowledge of the composition and geometry of the interfacial region between the droplet and the underlying substrate. In this work we introduce a 3D quantitative method for direct nanoscale visualization of such interfaces. Specifically, we demonstrate direct nano- to microscale imaging of complex fluidic interfaces using cryostabilization in combination with cryogenic focused ion beam milling and SEM imaging. We show that application of this method yields quantitative information about the interfacial geometry of water condensate on superhydrophilic, superhydrophobic, and lubricant-impregnated surfaces with previously unattainable nanoscale resolution. This type of information is crucial to a fundamental understanding as well as the design of surfaces with special wetting properties. PMID:23020195

  3. Effect of many-body interactions on the solid-liquid phase behavior of charge-stabilized colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Dobnikar, J.; Rzehak, R.; von Grünberg, H. H.

    2003-03-01

    The solid-liquid phase diagram of charge-stabilized colloidal suspensions has been calculated using a technique that combines a continuous Poisson-Boltzmann description for the microscopic electrolyte ions with a molecular-dynamics simulation for the macroionic colloidal spheres. While correlations between the microions are neglected in this approach, many-body interactions between the colloids, mediated by the screening ionic fluid between them, are fully included. The Lindemann criterion has been used to determine the solid-to-liquid transition temperature in a colloidal system at a relatively high colloid volume fraction where many-body interactions are expected to be strong. With a view to the Derjaguin-Landau-Verwey-Overbeek theory predicting that colloids interact via Yukawa pair potentials, we compare our results with the phase diagram of a simple Yukawa liquid. We find an agreement under high-salt conditions, but considerable differences at low ionic strength. Using effective force calculations and data from molecular-dynamics simulations with simple model potentials, we further demonstrate that these differences are due to many-body interactions.

  4. Using scanning electrochemical microscopy to probe chemistry at the solid-liquid interface in chemically amplified immersion lithography

    NASA Astrophysics Data System (ADS)

    LeSuer, Robert J.; Fan, Fu-Ren F.; Bard, Allen J.; Taylor, J. Christopher; Tsiartas, Pavlos; Willson, Grant; Conley, Willard E.; Feit, Gene; Kunz, Roderick R.

    2004-05-01

    Three modes of scanning electrochemical microscopy (SECM) - voltammetry, pH, and conductivity - have been used to better understand the chemistry at, and diffusion through, the solid/liquid interface formed between a resist film and water in 193 nm immersion lithography. Emphasis has been placed on investigating the photoacid generator (PAG), triphenylsulfonium perfluorobutanesulfonate, and the corresponding photoacid. The reduction of triphenylsulfonium at a hemispherical Hg microelectrode was monitored using square wave voltammetry to detect trace amounts of the PAG leaching from the surface. pH measurements at a 100 μm diameter Sb microelectrode show the formation of acid in the water layer above a resist upon exposure with UV irradiation. Bipolar conductance measurements at a 100 μm Pt tip positioned 100 μm from the surface indicate that the conductivity of the solution during illumination is dependent upon the percentage of PAG in the film. Liquid chromatography mass spectrometric analysis of water samples in contact with resist films has been used to quantify the amounts (< 10 ng/cm2) of PAG leaching from the film in the dark which occurs within the first 30 seconds of contact time. Washing the film removes approximately 80% of the total leachable PAG.

  5. Arrhenian and Non-Arrhenian Temperature Dependent Relaxation Time Development in the Solid-Liquid Transition Area of Amorphous Bodies

    NASA Astrophysics Data System (ADS)

    Hlaváček, Bořivoj; Drašar, Čestmír; Kalendová, Andréa; Menc, Pavel; Veselý, David

    The temperature-dependent changes of molecular and sub-molecular motions are studied in amorphous substances. The solid and liquid phases of amorphous bodies are characterized at the micro-level by two types of oscillators, linear and non-linear. It is accepted that an amorphous liquid is formed by domains that group the linear oscillators into the form of icebergs. The serial connection of the viscoelastic elements are arranged inside of these icebergs. The size of the linear connection within the domains is characterized by the number "n", which increases during the cooling process. The linear viscoelastic behavior of the individual serial connections is connected to the individual relaxation processes α, β, and γ. Only the "alpha" process exhibits growth of "n" to infinity on cooling. Therefore, the corresponding relaxation time, τα, for the infinite chain of "n" elements (Voigt or Maxwell elements) can also reach infinity as the material transforms to a glassy state. In contrast to the "alpha" process, the β and γ processes are limited in growth for serial connections in a chain structure. Therefore, the relaxation times for the β and γ processes, τβ and τγ, will only follow the temperature dependence of the sample viscosity on cooling, which is, of course, Arrhenian. We discuss the role of non-linear oscillators in the solid-liquid transition in relation to Brownian motion.

  6. The research on particle trajectory of solid-liquid two-phase flow and erosion predicting in screw centrifugal pump

    NASA Astrophysics Data System (ADS)

    Shen, Z. J.; Li, R. N.; Han, W.; Zhao, W. G.; Wang, X. H.

    2016-05-01

    Use the Discrete Phase Model (DPM) based on Euler-Lagrange method, the internal flow field of screw centrifugal pump was simulated by computational fluid dynamics(CFD) code when transmission medium is solid-liquid two phase flow with large-size particles. The research of liquid phase is under the Euler coordinate system while the solid phase is under the Lagrange coordinate system. The energy change, trajectory characteristic of solid phase particle and its erosion damage rule of solid-phase particle in whole computational domain is analyzed with different density, partical size(d=0.05mm, d=0.2mm, d=2mm) and solid volume fraction(Cv=3%, Cv=5%, Cv=7%).The result shows that within a given diameter range, the low density fine particles trajectory are longer, more collision times with flow passage components, more energy loss and the erosion parts are relatively uniform, but particles which are large-size diameter and high density has a big collision angle with the surface of impeller and volute, even the area of impact and abrasion are quite focus, and easy to be transported. particles will impact with the head of impeller when it enter into impeller domain, the erosion mainly occurs on the work side of impeller.

  7. Structural ordering at solid-liquid interfaces in Al-Sm system: A molecular-dynamics study

    DOE PAGESBeta

    Sun, Yang; Zhang, Feng; Ye, Zhuo; Ding, Zejun; Mendelev, Mikhail I.; Kramer, Matthew J.; Wang, Cai -Zhuang; Ho, Kai -Ming

    2016-07-12

    The structural ordering at solid-liquid interfaces far from equilibrium is studied with molecular dynamics simulations for the Al-Sm system. Using the van-Hove self-correlation function as the criterion to identify attachment/detachment events that occur at the interface, we are able to determine the time-dependent interface position, and characterize the detailed interfacial structure ordering surrounding the attached atoms. For the interface between an undercooled Al90Sm10 liquid and a metastable cubic structure, the solid induces the crystalline order of the cubic phase in the liquid layers, promoting the continuous growth of the crystal phase. When the same liquid is put in contact withmore » f.c.c. Al, Sm from the liquid can still attach to the solid interface despite its insolubility in the Al lattice. Non-f.c.c. order is revealed surrounding the attached Sm atoms. Lastly, we show that the local structure ordering at interface is highly correlated to solid packing and liquid ordering.« less

  8. Interaction mechanism of in-situ nano-TiN-AlN particles and solid/liquid interface during solidification.

    PubMed

    Cui, Chunxiang; Li, Yanchun; Shen, Yutian; Sun, Jibing; Wang, Ru

    2003-10-01

    This paper deals with the interaction mechanism between in situ nanometer-grade TiN-AlN particles and the solid/liquid (S/L) interface during the solidification of an in situ TiN-AlN/Al composite. According to the setting of a force balance for the particles in front of the S/L interface during solidification, F = F(buoyant) + F(repulsive) + F(viscous). We obtained the relationship between the critical cooling velocity of the liquid composite, Vr, and the size of the ceramic particle, rp. By this relationship formula, we can know that the S/L interface engulfs particles or pushes them to the crystal grain boundary during the solidification of a TiN-AlN/Al composite. It is found that Vr is proportional to the radius of ceramic particles by transmission electron microscope (TEM) observation. The TEM test indicates that the smaller the particle is, the more easily the S/L interface engulfs particles. PMID:14733152

  9. Toluene biodegradation in a solid/liquid system involving immobilized activated sludge and silicone oil as pollutant reservoir.

    PubMed

    Diz Castro, Manuel; Gómez-Díaz, Diego; Amrane, Abdeltif; Couvert, Annabelle

    2015-01-01

    A solid/liquid system involving activated sludge immobilized in an agar medium and a non-aqueous phase liquid containing the target pollutant has been considered to treat a model hydrophobic volatile organic compound, toluene. The positive impact of the use of a multiphase bioreactor is that the organic phase constitutes a pollutant reservoir and also helps to overcome possible pollutant toxicity. In addition and to overcome the drawbacks of the use of a solid organic phase (high pressure drop and low mass transfer) instead of a liquid organic phase, the considered solid phase was the aqueous. Consequently, silicone oil (polydimethylsiloxane) which showed its relevance for implementation in multiphase bioreactors was used. Promising results were observed from the analysis of toluene in the gaseous phase; for an initial amount of 2 g L(-1) related to the organic phase, a v/v ratio of 0.5 of the organic phase to the aqueous agar phase, total toluene consumption was observed in about 9 days, leading to a global biodegradation rate of approximately 3.1 mg L(-1) h(-1), namely in the range of values previously observed in liquid/liquid systems. PMID:25187471

  10. Solid-liquid interfacial energy of neopentylglycol solid solution in equilibrium with neopentylglycol-(D) camphor eutectic liquid

    NASA Astrophysics Data System (ADS)

    Bayram, Ü.; Aksöz, S.; Maraşlı, N.

    2012-01-01

    The grain boundary groove shapes for equilibrated solid neopentylglycol (NPG) solution (NPG-3 mol% D-camphor) in equilibrium with the NPG-DC eutectic liquid (NPG-36.1 mol% D-camphor) have been directly observed using a horizontal linear temperature gradient apparatus. From the observed grain boundary groove shapes, the Gibbs-Thomson coefficient ( Г), solid-liquid interfacial energy ( σSL) of NPG solid solution have been determined to be (7.5±0.7)×10 -8 K m and (8.1±1.2)×10 -3 J m -2, respectively. The Gibbs-Thomson coefficient versus TmΩ1/3, where Ω is the volume per atom was also plotted by linear regression for some organic transparent materials and the average value of coefficient ( τ) for nonmetallic materials was obtained to be 0.32 from graph of the Gibbs-Thomson coefficient versus TmΩ1/3. The grain boundary energy of solid NPG solution phase has been determined to be (14.6±2.3)×10 -3 J m -2 from the observed grain boundary groove shapes. The ratio of thermal conductivity of equilibrated eutectic liquid to thermal conductivity of solid NPG solution was also measured to be 0.80.

  11. Solid-Liquid Interfacial Energy of Solid Succinonitrile in Equilibrium with Succinonitrile-(D)Camphor-Aminomethylpropanediol Eutectic Liquid

    NASA Astrophysics Data System (ADS)

    Ata, Pınar; Karamazı, Yasin; Bayram, Ümit; Aksöz, Sezen; Keşlioğlu, Kazım; Maraşlı, Necmettin

    2016-01-01

    The grain boundary groove shapes for equilibrated solid SCN in equilibrium with the eutectic liquid SCN-15.6 mol% DC-2.1 mol% AMPD have been directly observed by using a horizontal linear temperature gradient apparatus. The ratio of the thermal conductivity of the equilibrated liquid to the thermal conductivity of solid SCN has also been determined to be 0.89. From the observed grain boundary groove shapes and measured thermal conductivity ratio, the Gibbs-Thomson coefficient ({{\\varGamma }}), solid-liquid interfacial energy (σ _{SL}), and the grain boundary energy (σ _{gb}) have been determined to be (5.43 ± 0.54)× 10^{-8} K{\\cdot } m, (8.53 ± 1.28) × 10^{-3} J {\\cdot } m^{-2}, and (13.36 ± 2.14) × 10^{-3} J{\\cdot } m^{-2}, respectively, for equilibrated solid SCN in equilibrium with the eutectic liquid (SCN-15.6 mol% DC-2.1 mol% AMPD).

  12. Study on solid-liquid two-phase unsteady flow characteristics with different flow rates in screw centrifugal pump

    NASA Astrophysics Data System (ADS)

    Li, R. N.; Y Wang, H.; Han, W.; Ma, W.; Shen, Z. J.

    2013-12-01

    The screw centrifugal pump is used as an object, and the unsteady numerical simulation of solid-liquid two-phase flow is carried out under different flow rate conditions in one circle by choosing the two-phase flow of sand and water as medium, using the software FLUENT based on the URANS equations, combining with sliding mesh method, and choosing the Mixture multiphase flow model and the SIMPLE algorithm. The results show that, with the flow rate increasing, the change trends for the pressure on volute outlet are almost constant, the fluctuation trends of the impeller axial force have a little change, the pressure and the axial force turn to decrease on the whole, the radial force gradually increases when the impeller maximum radius passes by half a cycle near the volute outlet, and the radial force gradually decreases when the maximum radius passes by the other half a cycle in a rotation cycle. The distributions of the solid particles are very uneven under a small flow rate condition on the face. The solid particles under a big flow rate condition are distributed more evenly than the ones under a small flow rate condition on the back. The theoretical basis and reference are provided for improving its working performance.

  13. Influences of solid/liquid boundary layer thickness and tilting angle on zone-refinement of germanium crystals

    NASA Astrophysics Data System (ADS)

    Yang, Gang; Guan, Yutong; Mei, Hao; Wang, Guojian; Mei, Dongming

    In zone-refining of metals, solid/liquid (S/L) boundary layer thickness has an influence on segregation coefficient of impurity atoms. Additionally, the segregation of impurity elements during zone refining can be maximized by adjusting the zone refinement tube with a proper angle. In this paper, we report the influences of S/L boundary layer thickness on the segregation coefficients of boron, phosphor, aluminum and gallium, which have been identified as four main impurities in germanium crystal by Photothermal Ionization Spectroscopy (PTIS). The thickness of S/L boundary layer was found by using a well-known model to fit the experimental data. The optimized segregation coefficients have been used to calculate the impurity distribution along the purified ingot. In addition, we have also optimized the tilting angle of the germanium ingot to investigate the impact on the segregation. This work is supported by DOE grant DE-FG02-10ER46709 and the state of South Dakota.

  14. Thermodynamic and rheological properties of solid-liquid systems in coal processing. Final technical report

    SciTech Connect

    Kabadi, V.N.

    1995-06-30

    The work on this project was initiated on September 1, 1991. The project consisted of two different tasks: (1) Development of a model to compute viscosities of coal derived liquids, and (2) Investigate new models for estimation of thermodynamic properties of solid and liquid compounds of the type that exist in coal, or are encountered during coal processing. As for task 1, a model for viscosity computation of coal model compound liquids and coal derived liquids has been developed. The detailed model is presented in this report. Two papers, the first describing the pure liquid model and the second one discussing the application to coal derived liquids, are expected to be published in Energy & Fuels shortly. Marginal progress is reported on task 2. Literature review for this work included compilation of a number of data sets, critical investigation of data measurement techniques available in the literature, investigation of models for liquid and solid phase thermodynamic computations. During the preliminary stages it was discovered that for development of a liquid or solid state equation of state, accurate predictive models for a number of saturation properties, such as, liquid and solid vapor pressures, saturated liquid and solid volumes, heat capacities of liquids and solids at saturation, etc. Most the remaining time on this task was spent in developing predictive correlations for vapor pressures and saturated liquid volumes of organic liquids in general and coal model liquids in particular. All these developments are discussed in this report. Some recommendations for future direction of research in this area are also listed.

  15. Detailed monitoring of two biogas plants and mechanical solid-liquid separation of fermentation residues.

    PubMed

    Bauer, Alexander; Mayr, Herwig; Hopfner-Sixt, Katharina; Amon, Thomas

    2009-06-01

    The Austrian "green electricity act" (Okostromgesetz) has led to an increase in biogas power plant size and consequently to an increased use of biomass. A biogas power plant with a generating capacity of 500 kW(el) consumes up to 38,000 kg of biomass per day. 260 ha of cropland is required to produce this mass. The high water content of biomass necessitates a high transport volume for energy crops and fermentation residues. The transport and application of fermentation residues to farmland is the last step in this logistic chain. The use of fermentation residues as fertilizer closes the nutrient cycle and is a central element in the efficient use of biomass for power production. Treatment of fermentation residues by separation into liquid and solid phases may be a solution to the transport problem. This paper presents detailed results from the monitoring of two biogas plants and from the analysis of the separation of fermentation residues. Furthermore, two different separator technologies for the separation of fermentation residues of biogas plants were analyzed. The examined biogas plants correspond to the current technological state of the art and have designs developed specifically for the utilization of energy crops. The hydraulic retention time ranged between 45.0 and 83.7 days. The specific methane yields were 0.40-0.43 m(3)N CH(4) per kg VS. The volume loads ranged between 3.69 and 4.00 kg VS/m(3). The degree of degradation was between 77.3% and 82.14%. The screw extractor separator was better suited for biogas slurry separation than the rotary screen separator. The screw extractor separator exhibited a high throughput and good separation efficiency. The efficiency of slurry separation depended on the dry matter content of the fermentation residue. The higher the dry matter content, the higher the proportion of solid phase after separation. In this project, we found that the fermentation residues could be divided into 79.2% fluid phase with a dry matter

  16. Thermodynamic study of binary system Propafenone Hydrocloride with Metoprolol Tartrate: solid-liquid equilibrium and compatibility with α-lactose monohydrate and corn starch.

    PubMed

    Marinescu, Daniela-Crina; Pincu, Elena; Meltzer, Viorica

    2013-05-20

    Solid-liquid equilibrium (SLE) for binary mixture of Propafenone Hydrocloride (PP) with Metoprolol Tartrate (MT) was investigated using differential scanning calorimetry (DSC) and corresponding activity coefficients were calculated. Simple eutectic behavior for this system was observed. The excess thermodynamic functions: G(E) and S(E) for the pre-, post-, and eutectic composition have been obtained using the computed activity coefficients data of the eutectic phase with their excess chemical potentials μi(E) (i=1, 2). The experimental solid-liquid phase temperatures were compared with predictions obtained from available eutectic equilibrium models. The results indicate non-ideality in this mixture. Also, the compatibility of each component and their eutectic mixture with usual excipients was investigated, and the DSC experiments indicate possible weak interactions with α-lactose monohydrate and compatibility with corn starch. The results obtained were confirmed by FT-IR measurements. PMID:23545398

  17. Thermodynamic and rheological properties of solid-liquid systems in coal processing. Quarterly technical report, March 1, 1992--May 31, 1992

    SciTech Connect

    Kabadi, V.N.; Ilias, S.

    1992-12-31

    In this report we present two data sets that have been compiled to assist in the model developments for solid-liquid equilibria and viscosities of coal derived systems. The first one is on vapor pressures of solid aromatics and the second one consists of viscosities of pure model compounds and some mixtures. These databanks are ready for usage in model development and are summarized in Tables 1 and 2. Literature is being searched to compile similar data for high pressure liquid compressibilities, liquid and solid heat capacities and solid-liquid equilibria for model compound systems. Literature search is also containing to investigate available viscosity models. Once this is completed a few models will be selected for evaluation and consideration as candidates for extension to coal liquids.

  18. Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface

    PubMed Central

    Axnanda, Stephanus; Crumlin, Ethan J.; Mao, Baohua; Rani, Sana; Chang, Rui; Karlsson, Patrik G.; Edwards, Mårten O. M.; Lundqvist, Måns; Moberg, Robert; Ross, Phil; Hussain, Zahid; Liu, Zhi

    2015-01-01

    We report a new method to probe the solid-liquid interface through the use of a thin liquid layer on a solid surface. An ambient pressure XPS (AP-XPS) endstation that is capable of detecting high kinetic energy photoelectrons (7 keV) at a pressure up to 110 Torr has been constructed and commissioned. Additionally, we have deployed a “dip & pull” method to create a stable nanometers-thick aqueous electrolyte on platinum working electrode surface. Combining the newly constructed AP-XPS system, “dip & pull” approach, with a “tender” X-ray synchrotron source (2 keV–7 keV), we are able to access the interface between liquid and solid dense phases with photoelectrons and directly probe important phenomena occurring at the narrow solid-liquid interface region in an electrochemical system. Using this approach, we have performed electrochemical oxidation of the Pt electrode at an oxygen evolution reaction (OER) potential. Under this potential, we observe the formation of both Pt2+ and Pt4+ interfacial species on the Pt working electrode in situ. We believe this thin-film approach and the use of “tender” AP-XPS highlighted in this study is an innovative new approach to probe this key solid-liquid interface region of electrochemistry. PMID:25950241

  19. The effects of liquid composition, temperature, and pressure on the equilibrium dihedral angles of binary solid-liquid systems inferred from a lattice-like model

    NASA Astrophysics Data System (ADS)

    Takei, Yasuko; Shimizu, Ichiko

    2003-10-01

    Dihedral angles of binary eutectic systems, such as silicate+melt systems, silicate+H 2O systems, binary alloys, and binary organic systems, tend to decrease with increasing concentration of the solid component in the liquid phase. This empirical law is useful to estimate dihedral angles in the Earth's interior from phase diagrams of solid-liquid systems. In this paper, we investigate the mechanism underlying this empirical law. By employing a lattice-like model in which the liquid phase is treated as a regular solution, we clarify the liquid composition, temperature, and pressure effects on the solid-liquid interfacial tension. It is shown that the non-ideality in chemical bonding causes a strong compositional dependence of the solid-liquid interfacial tension; due to the non-ideality in chemical bonding, the solid surface preferentially adsorbs the solid component, which results in the decrease of the interfacial tension with increasing concentration of this component in the bulk liquid phase. With this effect, the significant decrease of the dihedral angle with T observed in the SiO 2-H 2O system near the monotectic temperature, and the decrease with P observed in the forsterite-H 2O system, can be explained semi-quantitatively.

  20. Thermoelectric Magnetohydrodynamic Flows and Their Induced Change of Solid-Liquid Interface Shape in Static Magnetic Field-Assisted Directional Solidification

    NASA Astrophysics Data System (ADS)

    Wang, Jiang; Fautrelle, Yves; Nguyen-Thi, Henri; Reinhart, Guillaume; Liao, Hanlin; Li, Xi; Zhong, Yunbo; Ren, Zhongming

    2016-03-01

    Applying static magnetic field can produce flows (thermoelectric magnetohydrodynamic flows, TEMHDF) in the melt by interacting with the thermoelectric currents (TEC) during solidification of metals. A physical model was proposed to interpret how these TEC appear at the solid-liquid interface and verified by a corresponding simulation. The influences of TEMHDF on solidification were investigated through both ex-situ experiments and n situ observations by means of synchrotron X-ray radiography. The 3D numerical simulations of TEMHDF were performed for these two cases, respectively, and suggested that both the change of interface shape with different transverse static magnetic fields demonstrated by the ex-situ experiments and the real time observed interface shape varying under a 0.08 T transverse static magnetic field could attribute to the TEMHDF advanced solid-liquid interface in the static magnetic field-assisted directional solidification. The TEMHDF produced by an axial static magnetic field were also computed along with the interface change predicted based on which is good in line with the published experimental results. This study of TEMHDF and their impacts on the solid-liquid interface shape provides a method to tailor the structure during directional solidification using static magnetic field.

  1. Using “Tender” x-ray ambient pressure x-Ray photoelectron spectroscopy as a direct probe of solid-liquid interface

    SciTech Connect

    Axnanda, Stephanus; Crumlin, Ethan J.; Mao, Baohua; Rani, Sana; Chang, Rui; Karlsson, Patrik G.; Edwards, Mårten O. M.; Lundqvist, Måns; Moberg, Robert; Ross, Phil; Hussain, Zahid; Liu, Zhi

    2015-05-07

    We report a new method to probe the solid-liquid interface through the use of a thin liquid layer on a solid surface. An ambient pressure XPS (AP-XPS) endstation that is capable of detecting high kinetic energy photoelectrons (7 keV) at a pressure up to 110 Torr has been constructed and commissioned. Additionally, we have deployed a “dip & pull” method to create a stable nanometers-thick aqueous electrolyte on platinum working electrode surface. Combining the newly constructed AP-XPS system, “dip & pull” approach, with a “tender” X-ray synchrotron source (2 keV–7 keV), we are able to access the interface between liquid and solid dense phases with photoelectrons and directly probe important phenomena occurring at the narrow solid-liquid interface region in an electrochemical system. Using this approach, we have performed electrochemical oxidation of the Pt electrode at an oxygen evolution reaction (OER) potential. Under this potential, we observe the formation of both Pt²⁺ and Pt⁴⁺ interfacial species on the Pt working electrode in situ. We believe this thin-film approach and the use of “tender” AP-XPS highlighted in this study is an innovative new approach to probe this key solid-liquid interface region of electrochemistry.

  2. Using “Tender” x-ray ambient pressure x-Ray photoelectron spectroscopy as a direct probe of solid-liquid interface

    DOE PAGESBeta

    Axnanda, Stephanus; Crumlin, Ethan J.; Mao, Baohua; Rani, Sana; Chang, Rui; Karlsson, Patrik G.; Edwards, Mårten O. M.; Lundqvist, Måns; Moberg, Robert; Ross, Phil; et al

    2015-05-07

    We report a new method to probe the solid-liquid interface through the use of a thin liquid layer on a solid surface. An ambient pressure XPS (AP-XPS) endstation that is capable of detecting high kinetic energy photoelectrons (7 keV) at a pressure up to 110 Torr has been constructed and commissioned. Additionally, we have deployed a “dip & pull” method to create a stable nanometers-thick aqueous electrolyte on platinum working electrode surface. Combining the newly constructed AP-XPS system, “dip & pull” approach, with a “tender” X-ray synchrotron source (2 keV–7 keV), we are able to access the interface between liquidmore » and solid dense phases with photoelectrons and directly probe important phenomena occurring at the narrow solid-liquid interface region in an electrochemical system. Using this approach, we have performed electrochemical oxidation of the Pt electrode at an oxygen evolution reaction (OER) potential. Under this potential, we observe the formation of both Pt²⁺ and Pt⁴⁺ interfacial species on the Pt working electrode in situ. We believe this thin-film approach and the use of “tender” AP-XPS highlighted in this study is an innovative new approach to probe this key solid-liquid interface region of electrochemistry.« less

  3. Using “Tender” X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface

    NASA Astrophysics Data System (ADS)

    Axnanda, Stephanus; Crumlin, Ethan J.; Mao, Baohua; Rani, Sana; Chang, Rui; Karlsson, Patrik G.; Edwards, Mårten O. M.; Lundqvist, Måns; Moberg, Robert; Ross, Phil; Hussain, Zahid; Liu, Zhi

    2015-05-01

    We report a new method to probe the solid-liquid interface through the use of a thin liquid layer on a solid surface. An ambient pressure XPS (AP-XPS) endstation that is capable of detecting high kinetic energy photoelectrons (7 keV) at a pressure up to 110 Torr has been constructed and commissioned. Additionally, we have deployed a “dip & pull” method to create a stable nanometers-thick aqueous electrolyte on platinum working electrode surface. Combining the newly constructed AP-XPS system, “dip & pull” approach, with a “tender” X-ray synchrotron source (2 keV-7 keV), we are able to access the interface between liquid and solid dense phases with photoelectrons and directly probe important phenomena occurring at the narrow solid-liquid interface region in an electrochemical system. Using this approach, we have performed electrochemical oxidation of the Pt electrode at an oxygen evolution reaction (OER) potential. Under this potential, we observe the formation of both Pt2+ and Pt4+ interfacial species on the Pt working electrode in situ. We believe this thin-film approach and the use of “tender” AP-XPS highlighted in this study is an innovative new approach to probe this key solid-liquid interface region of electrochemistry.

  4. Numerical Calculation of the Drag Force Acting on a Solid Particle Pushed by a Solid/Liquid Interface

    NASA Technical Reports Server (NTRS)

    Catalina, Adrian V.; Stefanescu, Doru M.; Sen, Subhayu

    2000-01-01

    The distribution of insoluble particles in a metal casting depends primarily on the interaction of the particles with the solid/liquid interface (SLI) during the solidification process. The balance of the forces acting on the particle essentially determines whether a particle will be engulfed or pushed by the SLI. An important component of this force balance is the drag force generated by the particle motion in front of the SLI. Previously developed mathematical models for particle/SLI interaction made use of steady-state solutions of this force provided by the lubrication theory. However, our numerical model based on the SLI tracking approach shows that the steady-state approach is inappropriate to model the interaction process and that at steady-state the theoretical solution underestimates the drag force. It was found that regression analysis of steady-state numerical solutions for cylindrical particles moving normal to a flat SLI gives a relationship of the form: Abstract The distribution of insoluble particles in a metal casting depends primarily on the interaction of the particles with the solid/liquid interface (SLI) during the solidification process. The balance of the forces acting on the particle essentially determines whether a particle will be engulfed or pushed by the SLI. An important component of this force balance is the drag force generated by the particle motion in front of the SLI. Previously developed mathematical models for particle/SLI interaction made use of steady-state solutions of this force provided by the lubrication theory. However, our numerical model based on the SLI tracking approach shows that the steady-state approach is inappropriate to model the interaction process and that at steady-state the theoretical solution underestimates the drag force. It was found that regression analysis of steady-state numerical solutions for cylindrical particles moving normal to a flat SLI gives a relationship of the form: F(sub D, sup num) =sqoare

  5. Order-parameter-aided temperature-accelerated sampling for the exploration of crystal polymorphism and solid-liquid phase transitions

    SciTech Connect

    Yu, Tang-Qing Vanden-Eijnden, Eric; Chen, Pei-Yang; Chen, Ming; Samanta, Amit; Tuckerman, Mark

    2014-06-07

    The problem of predicting polymorphism in atomic and molecular crystals constitutes a significant challenge both experimentally and theoretically. From the theoretical viewpoint, polymorphism prediction falls into the general class of problems characterized by an underlying rough energy landscape, and consequently, free energy based enhanced sampling approaches can be brought to bear on the problem. In this paper, we build on a scheme previously introduced by two of the authors in which the lengths and angles of the supercell are targeted for enhanced sampling via temperature accelerated adiabatic free energy dynamics [T. Q. Yu and M. E. Tuckerman, Phys. Rev. Lett. 107, 015701 (2011)]. Here, that framework is expanded to include general order parameters that distinguish different crystalline arrangements as target collective variables for enhanced sampling. The resulting free energy surface, being of quite high dimension, is nontrivial to reconstruct, and we discuss one particular strategy for performing the free energy analysis. The method is applied to the study of polymorphism in xenon crystals at high pressure and temperature using the Steinhardt order parameters without and with the supercell included in the set of collective variables. The expected fcc and bcc structures are obtained, and when the supercell parameters are included as collective variables, we also find several new structures, including fcc states with hcp stacking faults. We also apply the new method to the solid-liquid phase transition in copper at 1300 K using the same Steinhardt order parameters. Our method is able to melt and refreeze the system repeatedly, and the free energy profile can be obtained with high efficiency.

  6. Spectrofluorimetric determination of melatonin in kernels of four different Pistacia varieties after ultrasound-assisted solid-liquid extraction

    NASA Astrophysics Data System (ADS)

    Oladi, Elham; Mohamadi, Maryam; Shamspur, Tayebeh; Mostafavi, Ali

    2014-11-01

    Melatonin is normally consumed to regulate the body's biological cycle. However it also has therapeutic properties, such as anti-tumor, anti-aging and protects the immune system. There are some reports on the presence of melatonin in edible kernels such as walnuts, but the extraction of melatonin from pistachio kernels is reported here for the first time. For this, the methanolic extract of pistachio kernels was exposed to gas chromatography/mass spectrometry analysis which confirmed the presence of melatonin. A fluorescence-based method was applied for the determination of melatonin in different extracts. When excited at λ = 275 nm, the fluorescence emission intensity of melatonin was measured at λ = 366 nm. Ultrasound-assisted solid-liquid extraction was used for the extraction of melatonin from pistachio kernels prior to fluorimetric determination. To achieve the highest extraction recovery, the main parameters affecting the extraction efficiency such as extracting solvent type and volume, temperature, sonication time and pH were evaluated. Under the optimized conditions, a linear dependence of fluorescence intensity on melatonin concentration was observed in the range of 0.0040-0.160 μg mL-1, with a detection limit of 0.0036 μg mL-1. This method was applied successfully for measuring and comparing the melatonin content in the kernels of four different varieties of Pistacia including Ahmad Aghaei, Akbari, Kalle Qouchi and Fandoghi. In addition, the results obtained were compared with those obtained using GC/MS. A good agreement was observed indicating the reliability of the proposed method.

  7. Order-parameter-aided temperature-accelerated sampling for the exploration of crystal polymorphism and solid-liquid phase transitions

    PubMed Central

    Yu, Tang-Qing; Chen, Pei-Yang; Chen, Ming; Samanta, Amit; Vanden-Eijnden, Eric; Tuckerman, Mark

    2014-01-01

    The problem of predicting polymorphism in atomic and molecular crystals constitutes a significant challenge both experimentally and theoretically. From the theoretical viewpoint, polymorphism prediction falls into the general class of problems characterized by an underlying rough energy landscape, and consequently, free energy based enhanced sampling approaches can be brought to bear on the problem. In this paper, we build on a scheme previously introduced by two of the authors in which the lengths and angles of the supercell are targeted for enhanced sampling via temperature accelerated adiabatic free energy dynamics [T. Q. Yu and M. E. Tuckerman, Phys. Rev. Lett. 107, 015701 (2011)]. Here, that framework is expanded to include general order parameters that distinguish different crystalline arrangements as target collective variables for enhanced sampling. The resulting free energy surface, being of quite high dimension, is nontrivial to reconstruct, and we discuss one particular strategy for performing the free energy analysis. The method is applied to the study of polymorphism in xenon crystals at high pressure and temperature using the Steinhardt order parameters without and with the supercell included in the set of collective variables. The expected fcc and bcc structures are obtained, and when the supercell parameters are included as collective variables, we also find several new structures, including fcc states with hcp stacking faults. We also apply the new method to the solid-liquid phase transition in copper at 1300 K using the same Steinhardt order parameters. Our method is able to melt and refreeze the system repeatedly, and the free energy profile can be obtained with high efficiency. PMID:24907992

  8. Modeling migrations of slab-derived fluid in deep crust based on the considerations of solid phase deformation and wettability of solid-liquid system

    NASA Astrophysics Data System (ADS)

    Ohta, J.; Tokunaga, T.

    2012-12-01

    In deep crust, it is considered that the solid phase tends to keep its polycrystalline structure while it flows as highly-viscous fluid, and that the fluid phase flows through polycrystalline solid as porous flow. Here, the solid-framework is considered to change its bulk volume due to the changes of fluid volumetric fraction. In addition, wettability of solid-liquid system, which is expressed as solid-liquid dihedral angle, is also considered to affect internal pore structure. Thus, the solid-framework deformation and wettability of solid-liquid system are considered to influence fluid migration. In this research, we firstly constructed the permeability model to formulate a relationship among solid-liquid dihedral angle, fluid fraction, and permeability based on the energetic and textural considerations of grain boundary interface. The permeability and the fluid fraction under minimum interfacial energy condition were expressed as functions of solid-liquid dihedral angle from this model. Then, we found that permeability can be written as functions of the fluid fraction and the permeability under minimum interfacial energy condition. Secondly, we formulated the deformation of solid-framework and fluid flow through the deforming framework. The governing equations included solid bulk viscosity and solid shear viscosity as necessary parameters to describe the behavior. Based on the derived governing equations, the one-dimensional numerical simulations were conducted with different solid viscosities. From the results where solid bulk/shear viscosity was set to be 1020 Pa×s, intervals with relatively high fluid fraction were formed and the intervals showed attenuated fluctuation of their fluid volume fraction. On the other hand, the results where solid bulk/shear viscosity was set to be 1019 Pa×s did not show such fluctuation. The complex interaction among fluid fraction, permeability, and solid viscosity could contribute to the observed phenomena, and further

  9. A Raman Spectroscopy and High-Speed Video Experimental Study: The Effect of Pressure on the Solid-Liquid Transformation Kinetics of N-octane

    NASA Astrophysics Data System (ADS)

    Liu, C.; Wang, D.

    2015-12-01

    Phase transitions of minerals and rocks in the interior of the Earth, especially at elevated pressures and temperatures, can make the crystal structures and state parameters obviously changed, so it is very important for the physical and chemical properties of these materials. It is known that the transformation between solid and liquid is relatively common in nature, such as the melting of ice and the crystallization of mineral or water. The kinetics relevant to these transformations might provide valuable information on the reaction rate and the reaction mechanism involving nucleation and growth. An in-situ transformation kinetic study of n-octane, which served as an example for this type of phase transition, has been carried out using a hydrothermal diamond anvil cell (HDAC) and high-speed video technique, and that the overall purpose of this study is to develop a comprehensive understanding of the reaction mechanism and the influence of pressure on the different transformation rates. At ambient temperature, the liquid-solid transformation of n-octane first took place with increasing pressure, and then the solid phase gradually transformed into the liquid phase when the sample was heated to a certain temperature. Upon the cooling of the system, the liquid-solid transformation occurred again. According to the established quantitative assessments of the transformation rates, pressure and temperature, it showed that there was a negative pressure dependence of the solid-liquid transformation rate. However, the elevation of pressure can accelerate the liquid-solid transformation rate. Based on the calculated activation energy values, an interfacial reaction and diffusion dominated the solid-liquid transformation, but the liquid-solid transformation was mainly controlled by diffusion. This experimental technique is a powerful and effective tool for the transformation kinetics study of n-octane, and the obtained results are of great significance to the kinetics study

  10. Soins Aux Brules Apres Un Accident Nucleaire

    PubMed Central

    Bargues, L.; Donat, N.; Jault, P.; Leclerc, T.

    2010-01-01

    Summary Les lésions radiques sont dues le plus souvent à des radio-isotopes utilisés dans l’industrie. L’explosion d’un réacteur nucléaire, les armes nucléaires ou une attaque terroriste constituent un risque d’afflux massif de victimes brûlées. Les radiations ionisantes occasionnent des brûlures thermiques, des syndromes d’irradiation aiguë avec pancytopénie et des signes cutanés retardés. Après une période de latence, des symptômes cutanés apparaissent et leur profondeur est proportionnelle à la dose reçue. Les protocoles habituels de réanimation des brûlés s’appliquent ici. Les soins aux irradiés nécessitent aussi une mesure de l’irradiation et une décontamination par des personnels entraînés. En cas de catastrophe nucléaire, la priorité est d’optimiser les structures existantes et de préserver les moyens pour les patients ayant la plus forte probabilité de survie. Après un accident nucléaire isolé, les difficultés dans les centres de brûlés sont l’évaluation de la profondeur et les techniques chirurgicales de couverture cutanée. La préparation des moyens médicaux et des centres de brûlés est nécessaire pour faire face à la prise en charge de ces brûlures différentes et complexes. PMID:21991218