Science.gov

Sample records for colloid chemistry

  1. The colloidal chemistry of ceramic clays

    NASA Technical Reports Server (NTRS)

    Phelps, G. W.

    1984-01-01

    The colloidal chemistry and mineralogy of two argil minerals were studied. Deposits of kaolin and of ceramic clays in the United States and England are discussed for the probable mechanism of formation. The structural modifications of the bed, original material associated with the clays and the proper use of flocculants are discussed.

  2. The use of objects and methods of colloid chemistry in nanochemistry

    NASA Astrophysics Data System (ADS)

    Summ, Boris D.; Ivanova, Nina I.

    2000-11-01

    Experimental methods and theoretical concepts of colloid chemistry regarding their possible use in nanochemistry and nanotechnology are considered. The main types of disperse systems which can be regarded as nanosystems are distinguished. Some methods for the preparation of colloidal nanosystems are described. Conditions for extrapolation of phenomenological laws of colloid chemistry to nanosize objects are considered. Examples of self-organised colloidal structures are given. The bibliography includes 205 references.

  3. Chemistry of the colloidal group II-VI nanocrystal synthesis

    NASA Astrophysics Data System (ADS)

    Liu, Haitao

    In the last two decades, the field of nanoscience and nanotechnology has witnessed tremendous advancement in the synthesis and application of group II-VI colloidal nanocrystals. The synthesis based on high temperature decomposition of organometallic precursors has become one of the most successful methods of making group II-VI colloidal nanocrystals. This method is first demonstrated by Bawendi and coworkers in 1993 to prepare cadmium chalcogenide colloidal quantum dots and later extended by others to prepare other group II-VI quantum dots as well as anisotropic shaped colloidal nanocrystals, such as nanorod and tetrapod. This dissertation focuses on the chemistry of this type of nanocrystal synthesis. The synthesis of group II-VI nanocrystals was studied by characterizing the molecular structures of the precursors and products and following their time evolution in the synthesis. Based on these results, a mechanism was proposed to account for the reaction between the precursors that presumably produces monomer for the growth of nanocrystals. Theoretical study based on density functional theory calculations revealed the detailed free energy landscape of the precursor decomposition and monomer formation pathway. Based on the proposed reaction mechanism, a new synthetic method was designed that uses water as a novel reagent to control the diameter and the aspect ratio of CdSe and US nanorods.

  4. Chemistry of the Colloidal Group II-VI Nanocrystal Synthesis

    SciTech Connect

    Liu, Haitao

    2007-05-17

    In the last two decades, the field of nanoscience andnanotechnology has witnessed tremendous advancement in the synthesis andapplication of group II-VI colloidal nanocrystals. The synthesis based onhigh temperature decomposition of organometallic precursors has becomeone of the most successful methods of making group II-VI colloidalnanocrystals. This method is first demonstrated by Bawendi and coworkersin 1993 to prepare cadmium chalcogenide colloidal quantum dots and laterextended by others to prepare other group II-VI quantum dots as well asanisotropic shaped colloidal nanocrystals, such as nanorod and tetrapod.This dissertation focuses on the chemistry of this type of nanocrystalsynthesis. The synthesis of group II-VI nanocrystals was studied bycharacterizing the molecular structures of the precursors and productsand following their time evolution in the synthesis. Based on theseresults, a mechanism was proposed to account for the 2 reaction betweenthe precursors that presumably produces monomer for the growth ofnanocrystals. Theoretical study based on density functional theorycalculations revealed the detailed free energy landscape of the precursordecomposition and monomerformation pathway. Based on the proposedreaction mechanism, a new synthetic method was designed that uses wateras a novel reagent to control the diameter and the aspect ratio of CdSeand CdS nanorods.

  5. Chemistry of the Colloidal Group II-VI Nanocrystal Synthesis

    SciTech Connect

    Liu, Haitao

    2007-05-17

    In the last two decades, the field of nanoscience andnanotechnology has witnessed tremendous advancement in the synthesis andapplication of group II-VI colloidal nanocrystals. The synthesis based onhigh temperature decomposition of organometallic precursors has becomeone of the most successful methods of making group II-VI colloidalnanocrystals. This methodis first demonstrated by Bawendi and coworkersin 1993 to prepare cadmium chalcogenide colloidal quantum dots and laterextended by others to prepare other group II-VI quantum dots as well asanisotropic shaped colloidal nanocrystals, such as nanorod and tetrapod.This dissertation focuses on the chemistry of this type of nanocrystalsynthesis. The synthesis of group II-VI nanocrystals was studied bycharacterizing the molecular structures of the precursors and productsand following their time evolution in the synthesis. Based on theseresults, a mechanism was proposed to account for the 2 reaction betweenthe precursors that presumably produces monomer for the growth ofnanocrystals. Theoretical study based on density functional theorycalculations revealed the detailed free energy landscape of the precursordecomposition and monomerformation pathway. Based on the proposedreaction mechanism, a new synthetic method was designed that uses wateras a novel reagent to control the diameter and the aspect ratio of CdSeand CdS nanorods.

  6. Hysteresis of colloid retention and release in saturated porous media during transients in solution chemistry.

    PubMed

    Torkzaban, Saeed; Kim, Hyunjung N; Simunek, Jiri; Bradford, Scott A

    2010-03-01

    Saturated packed column and micromodel transport studies were conducted to gain insight on mechanisms of colloid retention and release under unfavorable attachment conditions. The initial deposition of colloids in porous media was found to be a strongly coupled process that depended on solution chemistry and pore space geometry. During steady state chemical conditions, colloid deposition was not a readily reversible process, and micromodel photos indicated that colloids were immobilized in the presence of fluid drag. Upon stepwise reduction in eluting solution ionic strength (IS), a sharp release of colloids occurred in each step which indicates that colloid retention depends on a balance of applied (hydrodynamic) and resisting (adhesive) torques which varied with pore space geometry, surface roughness, and interaction energy. When the eluting fluid IS was reduced to deionized water, the final retention locations occurred near grain-grain contacts, and colloid aggregation was sometimes observed in micromodel experiments. Significant amounts of colloid retention hysteresis with IS were observed in the column experiments, and it depended on the porous medium (glass beads compared with sand), the colloid size (1.1 and 0.5 mum), and on the initial deposition IS. These observations were attributed to weak adhesive interactions that depended on the double layer thickness (e.g., the depth of the secondary minimum and/or nanoscale heterogeneity), colloid mass transfer on the solid phase to regions where the torque and force balances were favorable for retention, the number and extent of grain-grain contacts, and surface roughness. PMID:20136144

  7. Challenges in Teaching "Colloid and Surface Chemistry"--A Danish Experience

    ERIC Educational Resources Information Center

    Kontogeorgis, Georgios M.; Vigild, Martin E.

    2009-01-01

    Seven years ago we were asked, as one of our first teaching duties at the Technical University of Denmark (DTU), to teach a 5 ECTS point course on "Colloid and Surface Chemistry". The topic is itself at the same time exciting and demanding, largely due to its multidisciplinary nature. Several "local" requirements posed additional challenges. The…

  8. Developing new synthetic methods for colloidal hybrid nanoparticles: Conversion chemistry and chemoselectivity

    NASA Astrophysics Data System (ADS)

    Bradley, Matthew

    Colloidal hybrid nanoparticles contain multiple domains, and through their solidsolid interfaces, can facilitate synergistic relationships between domains, resulting in the incorporation of multiple functionalities as well as modification of the intrinsic properties of each domain. Although there is a growing number of materials and applications associated with these unique types of particles, new synthetic methods must be investigated in order to realize the full potential of this new class of particles. To address this need, we demonstrate that the concepts used in total synthesis of complex organic molecules, can be applied to the synthesis of colloidal hybrid nanoparticles. Site selective growth, conversion chemistry, condensation chemistry, and protection/deprotection reactions are examined as ways to add complexity to colloidal hybrid nanoparticles. First, we will discuss the synthesis of PtPb-Fe3O4 and Pt3Sn-Fe3O4 heterodimer particles via a solution mediated conversion chemistry process. These types of reactions are known to be useful for nanoparticle systems but had not been explored as a method for adding complexity to colloidal heterodimers. Pt-Fe3O 4 heterodimers react with Pb(acac)2 and Sn(acac)2 at 180-200°C in a mixture of benzyl ether, oleylamine, oleic acid, and tert-butylamine borane to form PtPb-Fe3O4 and Pt3Sn-Fe3O4 heterodimers, respectively. This chemical transformation reaction introduces intermetallic and alloy components into the heterodimers, proceeds with morphological retention, and preserves the solid-solid interface that characterizes these hybrid nanoparticle systems. In addition, the PtPb-Fe3O4 heterodimers spontaneously aggregate to form colloidally stable (PtPb-Fe3O4) n nanoflowers via a process that is conceptually analogous to a molecular condensation reaction. Next, we will discuss the methanol oxidation activity of PtPb-Fe 3O4 and Pt3Sn- Fe3O4 heterodimers as well as examine the role of ligand exchange in this process. Before

  9. Surface chemistry : a non-negligible parameter in determining optical properties of small colloidal metal nanoparticles.

    SciTech Connect

    Sun, Y.; Gray, S. K.; Peng, S.

    2011-01-01

    Surface chemistry can become pronounced in determining the optical properties of colloidal metal nanoparticles as the nanoparticles become so small (diameters <20 nm) that the surface atoms, which can undergo chemical interactions with the environment, represent a significant fraction of the total number of atoms although this effect is often ignored. For instance, formation of chemical bonds between surface atoms of small metal nanoparticles and capping molecules that help stabilize the nanoparticles can reduce the density of conduction band electrons in the surface layer of metal atoms. This reduced electron density consequently influences the frequency-dependent dielectric constant of the metal atoms in the surface layer and, for sufficiently high surface to volume ratios, the overall surface plasmon resonance (SPR) absorption spectrum. The important role of surface chemistry is highlighted here by carefully analyzing the classical Mie theory and a multi-layer model is presented to produce more accurate predictions by considering the chemically reduced density of conduction band electrons in the outer shell of metal atoms in nanoparticles. Calculated absorption spectra of small Ag nanoparticles quantitatively agree with the experimental results for our monodispersed Ag nanoparticles synthesized via a well-defined chemical reduction process, revealing an exceptional size-dependence of absorption peak positions: the peaks first blue-shift followed by a turnover and a dramatic red-shift as the particle size decreases. A comprehensive understanding of the relationship between surface chemistry and optical properties is beneficial to exploit new applications of small colloidal metal nanoparticles, such as colorimetric sensing, electrochromic devices, and surface enhanced spectroscopies.

  10. A Study of Functional Polymer Colloids Prepared Using Thiol-Ene/Yne Click Chemistry

    NASA Astrophysics Data System (ADS)

    Durham, Olivia Z.

    This project demonstrates the first instance of thiol-ene chemistry as the polymerization method for the production of polymer colloids in two-phase heterogeneous suspensions, miniemulsions, and emulsions. This work was also expanded to thiol-yne chemistry for the production of polymer particles containing increased crosslinking density. The utility of thiol-ene and thiol-yne chemistries for polymerization and polymer modification is well established in bulk systems. These reactions are considered 'click' reactions, which can be defined as processes that are both facile and simple, offering high yields with nearly 100% conversion, no side products, easy product separation, compatibility with a diverse variety of commercially available starting materials, and orthogonality with other chemistries. In addition, thiol-ene and thiol-yne chemistry follow a step-growth mechanism for the development of highly uniform polymer networks, where polymer growth is dependent on the coupling of functional groups. These step-growth polymerization systems are in stark contrast to the chain-growth mechanisms of acrylic and styrenic monomers that have dominated the field of conventional heterogeneous polymerizations. Preliminary studies evaluated the mechanism of particle production in suspension and miniemulsion systems. Monomer droplets were compared to the final polymer particles to confirm that particle growth occurred through the polymerization of monomer droplets. Additional parameters examined include homogenization energy (mechanical mixing), diluent species and concentration, and monomer content. These reactions were conducted using photoinitiation to yield particles in a matter of minutes with diameters in the size range of several microns to hundreds of microns in suspensions or submicron particles in miniemulsions. Improved control over the particle size and size distribution was examined through variation of reaction parameters. In addition, a method of seeded suspension

  11. Surface chemistry investigation of colloid transport in packed beds. Final report, August 1, 1989--July 31, 1996

    SciTech Connect

    Olson, T.M.

    1996-12-31

    The importance of colloids as co-transport agents for pollutants in subsurface systems hinges on the extent to which electrostatic or other sources of repulsive colloid-collector interactions inhibit their filtration. When electrostatic interactions are favorable, for example when the colloid and groundwater media have opposite charge, colloids may be expected to travel only a few centimeters in saturated porous media. Repulsive electrostatic interactions between colloids and aquifer media with the same charge sign are postulated to significantly mobilize particles. As it happens, however, theories describing particle filtration from first principles, i.e., DLVO (Derjagin and Landau, Verwey and Overbeek) theory, dramatically underestimate filtration rates when colloid-collector interactions are electrostatically repulsive. One of the primary objectives of the project was to experimentally investigate potential reasons for the historical lack of agreement between particle filtration models based on DLVO theory and observed particle deposition rates. An important hypothesis of the study was to test the validity of the assumption of surface homogeneity, as required by these models. The approach was to focus on collector surfaces that were commonly used as model systems, e.g., glass beads and quartz sand. Laboratory-scale column filtration experiments were conducted with colloidal polystyrene latex spheres. Collector surface preparation and cleaning approaches were examined, as well as the effects of solution chemistry.

  12. A Study of Functional Polymer Colloids Prepared Using Thiol-Ene/Yne Click Chemistry

    NASA Astrophysics Data System (ADS)

    Durham, Olivia Z.

    This project demonstrates the first instance of thiol-ene chemistry as the polymerization method for the production of polymer colloids in two-phase heterogeneous suspensions, miniemulsions, and emulsions. This work was also expanded to thiol-yne chemistry for the production of polymer particles containing increased crosslinking density. The utility of thiol-ene and thiol-yne chemistries for polymerization and polymer modification is well established in bulk systems. These reactions are considered 'click' reactions, which can be defined as processes that are both facile and simple, offering high yields with nearly 100% conversion, no side products, easy product separation, compatibility with a diverse variety of commercially available starting materials, and orthogonality with other chemistries. In addition, thiol-ene and thiol-yne chemistry follow a step-growth mechanism for the development of highly uniform polymer networks, where polymer growth is dependent on the coupling of functional groups. These step-growth polymerization systems are in stark contrast to the chain-growth mechanisms of acrylic and styrenic monomers that have dominated the field of conventional heterogeneous polymerizations. Preliminary studies evaluated the mechanism of particle production in suspension and miniemulsion systems. Monomer droplets were compared to the final polymer particles to confirm that particle growth occurred through the polymerization of monomer droplets. Additional parameters examined include homogenization energy (mechanical mixing), diluent species and concentration, and monomer content. These reactions were conducted using photoinitiation to yield particles in a matter of minutes with diameters in the size range of several microns to hundreds of microns in suspensions or submicron particles in miniemulsions. Improved control over the particle size and size distribution was examined through variation of reaction parameters. In addition, a method of seeded suspension

  13. Hysteresis of Colloid Retention and Release in Saturated Porous Media During Transients in Solution Chemistry

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Saturated packed column and micromodel transport studies wereconducted to gain insightonmechanismsof colloid retention and release under unfavorable attachment conditions. The initial deposition of colloids in porous media was found to be a strongly coupled process that depended on solution chemistr...

  14. Revisiting the Fundamentals in the Design and Control of Nanoparticulate Colloids in the Frame of Soft Chemistry.

    PubMed

    Uskoković, Vuk

    2013-10-01

    This review presents thoughts on some of the fundamental features of conceptual models applied in the design of fine particles in the frames of colloid and soft chemistry. A special emphasis is placed on the limitations of these models, an acknowledgment of which is vital in improving their intricacy and effectiveness in predicting the outcomes of the corresponding experimental settings. Thermodynamics of self-assembly phenomena illustrated on the examples of protein assembly and micellization is analyzed in relation to the previously elaborated thesis that each self-assembly in reality presents a co-assembly, since it implies a mutual reorganization of the assembling system and its immediate environment. Parameters used in the design of fine particles by precipitation are discussed while referring to solubility product, various measures of supersaturation levels, induction time, nucleation and crystal growth rates, interfacial energies, and the Ostwald-Lussac law of phases. Again, the main drawbacks and inadequacies of using the aforementioned parameters in tailoring the materials properties in a soft and colloidal chemical setting were particularly emphasized. The basic and practical limitations of zeta-potential analyses, routinely used to stabilize colloidal dispersions and initiate specific interactions between soft chemical entities, were also outlined. The final section of the paper reiterates the unavoidable presence of practical qualitative models in the design and control of nanoparticulate colloids, which is supported by the overwhelming complexity of quantitative relationships that govern the processes of their formation and assembly. PMID:24490052

  15. Revisiting the Fundamentals in the Design and Control of Nanoparticulate Colloids in the Frame of Soft Chemistry1

    PubMed Central

    Uskoković, Vuk

    2013-01-01

    This review presents thoughts on some of the fundamental features of conceptual models applied in the design of fine particles in the frames of colloid and soft chemistry. A special emphasis is placed on the limitations of these models, an acknowledgment of which is vital in improving their intricacy and effectiveness in predicting the outcomes of the corresponding experimental settings. Thermodynamics of self-assembly phenomena illustrated on the examples of protein assembly and micellization is analyzed in relation to the previously elaborated thesis that each self-assembly in reality presents a co-assembly, since it implies a mutual reorganization of the assembling system and its immediate environment. Parameters used in the design of fine particles by precipitation are discussed while referring to solubility product, various measures of supersaturation levels, induction time, nucleation and crystal growth rates, interfacial energies, and the Ostwald–Lussac law of phases. Again, the main drawbacks and inadequacies of using the aforementioned parameters in tailoring the materials properties in a soft and colloidal chemical setting were particularly emphasized. The basic and practical limitations of zeta-potential analyses, routinely used to stabilize colloidal dispersions and initiate specific interactions between soft chemical entities, were also outlined. The final section of the paper reiterates the unavoidable presence of practical qualitative models in the design and control of nanoparticulate colloids, which is supported by the overwhelming complexity of quantitative relationships that govern the processes of their formation and assembly. PMID:24490052

  16. Equilibrium and kinetic models for colloid release under transient solution chemistry conditions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    We present continuum models to describe colloid release in the subsurface during transient physicochemical conditions. Our modeling approach relates the amount of colloid release to changes in the fraction of the solid surface area that contributes to retention. Equilibrium, kinetic, equilibrium and...

  17. The effect of artificial seawater on SERS spectra of amino acids-Ag colloids: an experiment of prebiotic chemistry.

    PubMed

    Nascimento, Fernanda C; Carneiro, Cristine E A; de Santana, Henrique; Zaia, Dimas A M

    2014-01-24

    The large enhancement of signal observed in surface enhanced Raman spectroscopy (SERS) could be helpful for identifying amino acids on the surface of other planets, in particular for Mars, as well as in prebiotic chemistry experiments of interaction minerals/amino acids. This paper reports the effect of several substances (NaCl, MgCl2, KBr, CaSO4, K2SO4, MgSO4, KI, NH4Cl, SrCl2, CaCl2, Na2SO4, KOH, NaOH, H3BO3) on the SERS spectra of colloid of sodium citrate-CSC and colloid of sodium borohydride-CSB. The effect of four different artificial seawaters and these artificial seawaters plus amino acids (α-Ala-alanine, Gly-glycine, Cys-cysteine, AIB-2-aminoisobutiric acid) on SERS spectra using both CSC and CSB was also studied. For CSC, the effect of water, after dilution of the colloid, was the appearance of several absorption bands belonging to sodium citrate in the SERS spectrum. In general, artificial seawaters enhanced several bands in SERS spectra using CSC and CSB and CSC was more sensitive to those artificial seawaters than CSB. The identification of Gly, α-Ala and AIB using CSC or CSB was not possible because several bands belonging to artificial seawaters, sodium citrate or sodium borohydride were enhanced. On the other hand, artificial seawaters did not interfere in the SERS spectra of Cys using CSC or CSB, although the interaction of Cys with each colloid was different. For CSC the band at 2568 cm(-1) (S-H stretching) of Cys vanished and for CSB the intensity of this band decreased, indicating the -SH of Cys was bonded to Ag to form -S-Ag. Thus SERS spectroscopy could be used for Cys detection on Mars soils using Mars land rovers as well as to study the interaction between Cys and minerals in prebiotic chemistry experiments. PMID:24051298

  18. Equilibrium and Kinetic Models for Colloid Release Under Transient Solution Chemistry Conditions

    NASA Astrophysics Data System (ADS)

    Bradford, S. A.; Torkzaban, S.; Leij, F. J.; Simunek, J.

    2014-12-01

    Colloid retention and release is well known to depend on a wide variety of physical, chemical, and microbiological factors that may vary temporally in the subsurface environment. We present equilibrium, kinetic, combined equilibrium and kinetic, and two-site kinetic models of colloid release during transient physicochemical conditions. Our mathematical modeling approach relates colloid release under transient conditions to changes in the fraction of the solid surface area that contributes to retention. The developed models were subsequently applied to experimental colloid release datasets to investigate the influence of variations in ionic strength (IS), pH, cation exchange, colloid size, and water velocity on release. Various combinations of equilibrium and/or kinetic release models were needed to describe the experimental data depending on the transient conditions and colloid type. Release of E. coli D21g was promoted by a decrease in solution IS and an increase in pH, similar to expected trends for a reduction in the secondary minimum and nanoscale chemical heterogeneity, respectively. The retention and release of 20 nm carboxyl modified latex nanoparticles (NPs) were demonstrated to be more sensitive to the presence of Ca2+ than D21g. Specifically, retention of NPs was greater than D21g in the presence of 2 mM CaCl2 solution, and release of NPs only occurred after exchange of Ca2+ by Na+ and then a reduction in the solution IS. These findings highlight the limitations of conventional interaction energy calculations to describe colloid retention and release, and point to the need to consider Born repulsion and nanoscale heterogeneity. Temporal changes in the water velocity did not have a large influence on the release of D21g. This insensitivity was likely due to factors that reduce the applied hydrodynamic torque and/or increase the resisting adhesive torque. Collectively, experimental and modeling results indicate that episodic colloid transport in the

  19. Equilibrium and kinetic models for colloid release under transient solution chemistry conditions.

    PubMed

    Bradford, Scott A; Torkzaban, Saeed; Leij, Feike; Simunek, Jiri

    2015-10-01

    We present continuum models to describe colloid release in the subsurface during transient physicochemical conditions. Our modeling approach relates the amount of colloid release to changes in the fraction of the solid surface area that contributes to retention. Equilibrium, kinetic, equilibrium and kinetic, and two-site kinetic models were developed to describe various rates of colloid release. These models were subsequently applied to experimental colloid release datasets to investigate the influence of variations in ionic strength (IS), pH, cation exchange, colloid size, and water velocity on release. Various combinations of equilibrium and/or kinetic release models were needed to describe the experimental data depending on the transient conditions and colloid type. Release of Escherichia coli D21g was promoted by a decrease in solution IS and an increase in pH, similar to expected trends for a reduction in the secondary minimum and nanoscale chemical heterogeneity. The retention and release of 20nm carboxyl modified latex nanoparticles (NPs) were demonstrated to be more sensitive to the presence of Ca(2+) than D21g. Specifically, retention of NPs was greater than D21g in the presence of 2mM CaCl2 solution, and release of NPs only occurred after exchange of Ca(2+) by Na(+) and then a reduction in the solution IS. These findings highlight the limitations of conventional interaction energy calculations to describe colloid retention and release, and point to the need to consider other interactions (e.g., Born, steric, and/or hydration forces) and/or nanoscale heterogeneity. Temporal changes in the water velocity did not have a large influence on the release of D21g for the examined conditions. This insensitivity was likely due to factors that reduce the applied hydrodynamic torque and/or increase the resisting adhesive torque; e.g., macroscopic roughness and grain-grain contacts. Our analysis and models improve our understanding and ability to describe the amounts

  20. Layered Double Hydroxide Nanoclusters: Aqueous, Concentrated, Stable, and Catalytically Active Colloids toward Green Chemistry.

    PubMed

    Tokudome, Yasuaki; Morimoto, Tsuyoshi; Tarutani, Naoki; Vaz, Pedro D; Nunes, Carla D; Prevot, Vanessa; Stenning, Gavin B G; Takahashi, Masahide

    2016-05-24

    Increasing attention has been dedicated to the development of nanomaterials rendering green and sustainable processes, which occur in benign aqueous reaction media. Herein, we demonstrate the synthesis of another family of green nanomaterials, layered double hydroxide (LDH) nanoclusters, which are concentrated (98.7 g/L in aqueous solvent), stably dispersed (transparent sol for >2 weeks), and catalytically active colloids of nano LDHs (isotropic shape with the size of 7.8 nm as determined by small-angle X-ray scattering). LDH nanoclusters are available as colloidal building blocks to give access to meso- and macroporous LDH materials. Proof-of-concept applications revealed that the LDH nanocluster works as a solid basic catalyst and is separable from solvents of catalytic reactions, confirming the nature of nanocatalysts. The present work closely investigates the unique physical and chemical features of this colloid, the formation mechanism, and the ability to act as basic nanocatalysts in benign aqueous reaction systems. PMID:27124717

  1. A Mechanistic Approach to Predicting Colloid Deposition onto Representative Aquifer Materials and Solution Chemistries in the Presence of an Energy Barrier

    NASA Astrophysics Data System (ADS)

    Trauscht, J. S.; Pazmino, E. F.; Johnson, W. P.

    2014-12-01

    Despite several decades of research we lack a mechanistic theory to predict deposition in porous media in the presence of colloid-collector repulsion (unfavorable conditions). Recently, mechanistic models have been developed that incorporate nanoscale surface heterogeneity in colloid-collector interactions. Comparisons of simulations to experimental data allows backing out a representative heterogeneity for the surface, which to date has been reported only for silica. Colloid deposition onto a variety of representative aquifer materials expected to be unfavorable under environmental conditions (quartz, muscovite and albite) was observed for 0.25, 1.1 and 1.95 μm carboxylate-modified latex microspheres using an impinging jet system. Deposition efficiencies varied in response to changes in collector mineralogy, ionic strength, electrolyte valence and pH. Collector surface charge heterogeneity characteristics (heterodomain size and spatial distribution) were backed out from these experiments via comparison to particle trajectory simulations incorporating discrete nano-scale attractive domains (heterodomains). A bi-modal distribution (1:4, ratio of large to small heterodomains) of 120nm and 60nm heterodomains was found to quantitatively predict retention for all three colloid sizes for a given surface. Varying the surface coverage of heterodomains allowed a characteristic coverage for each observed collector surface to be determined. This developing catalog of surface characteristics will aid prediction of colloid transport and deposition under environmentally relevant conditions (aquifer material composition and groundwater chemistry).

  2. Effect of surface chemistry on the morphology, resistance, and colloidal behavior of small silver particles

    NASA Astrophysics Data System (ADS)

    Schwab, Scott D.; McCreery, Richard L.; Cummings, Kevin D.

    1985-07-01

    Raman spectrometry, transmission electron microscopy, and elemental analysis were used to characterize small silver particles prepared by evaporation of silver from a molybdenum or tungsten boat into a reduced-pressure atmosphere of argon and oxygen. Particles prepared with both molybdenum and oxygen present were 50-400-Å-diam spheres, but much larger aspherical particles resulted if either molybdenum or oxygen was absent. The spherical particles were coated with approximately one monolayer of polymeric molybdenum oxide formed during fabrication from volatile MoO3. The polymolybdate-coated particles form a stable suspension in water and have high electrical resistance, while those prepared in the absence of molybdenum have low resistance and do not suspend in water. No evidence of silver oxide formation was obtained, even for particles prepared by silver evaporation in oxygen in the absence of molybdenum, We conclude that the polymolybdate coating prevents the formation of very large (>1000 Å) particles during fabrication. Furthermore, the coating becomes negatively charged in polar solvents, leading to formation of a stable colloidal suspension. Thus the molybdenum boat is essential for the fabrication of small spherical particles, and has a large effect on the properties of the final material. While silver oxide formation cannot be rigorously ruled out, it is clear that molybdenum, not silver, oxides determine the morphology and resistance of the particles.

  3. A Surface Chemistry Approach to Enhancing Colloidal Quantum Dot Solids for Photovoltaics

    NASA Astrophysics Data System (ADS)

    Carey, Graham Hamilton

    Colloidal quantum dot (CQD) photovoltaic devices have improved rapidly over the past decade of research. By taking advantage of the quantum confinement effect, solar cells constructed using films of infrared-bandgap nanoparticles are able to capture previously untapped ranges of the solar energy spectrum. Additionally, films are fabricated using simple, cheap, reproducible solution processing techniques, enabling the creation of low-cost, flexible photovoltaic devices. A key factor limiting the creation of high efficiency CQD solar cells is the short charge carrier diffusion length in films. Driven by a combination of limited carrier mobility, poor nanoparticle surface passivation, and the presence of unexamined electrically active impurities throughout the film, the poor diffusion length limits the active layer thickness in CQD solar cells, leading to lower-than-desired light absorption, and curtailing the photocurrent generated by such devices. This thesis seeks to address poor diffusion length by addressing each of the limiting factors in turn. Electrical transport in quantum dot solids is examined in the context of improved quantum dot packing; methods are developed to improve packing by using actively densifying components, or by dramatically lowering the volume change required between quantum dots in solution and in solid state. Quantum dot surface passivation is improved by introducing a crucial secondary, small halide ligand source, and by surveying the impact of the processing environment on the final quality of the quantum dot surface. A heretofore unidentified impurity present in quantum dot solids is identified, characterized, and chemically eliminated. Finally, lessons learned through these experiments are combined into a single, novel materials system, leading to quantum dot devices with a significantly improved diffusion length (enhanced from 70 to 230 nm). This enabled thick, high current density (30 mA cm -2, compared to typical values in the 20

  4. Colloidal stability of gold nanorod solution upon exposure to excised human skin: Effect of surface chemistry and protein adsorption.

    PubMed

    Mahmoud, Nouf N; Al-Qaoud, Khaled M; Al-Bakri, Amal G; Alkilany, Alaaldin M; Khalil, Enam A

    2016-06-01

    In this study, we evaluated the colloidal stability of gold nanorods (with positive, negative and neutral surface charge) in solution upon contact with excised human skin. UV-vis absorption, plasmon peak broadening index (PPBI%) and transmission electron microscope analysis were used to follow nanoparticles aggregation in solution. Our results show that positively charged gold nanorods aggregate extensively upon exposure to excised human skin compared to negatively and neutrally charged gold nanorods. Skin-induced aggregation of cationic gold nanorods was linked to the adsorption of proteins released from the dermis layer to the surface of gold nanorods. Protein adsorption significantly screen nanorod's effective surface charge and induce their aggregation. Moreover, we demonstrate that the presence of polyethylene glycol polymer on the surface of cationic gold nanorods minimize this aggregation significantly by providing steric repulsion (non-electrostatic stabilization mechanism). This work highlights the importance of evaluating the colloidal stability of nanoparticles in solution upon contact with skin, which is a "usually overlooked" parameter when studying the nanoparticle-skin interaction. PMID:26923289

  5. The Extension of Colloid Chemistry from Aqueous to Non-Aqueous Media with Application to Nanofluid Research

    NASA Astrophysics Data System (ADS)

    Clary, Dan

    Cyclodextrins are cyclic molecules composed of glucose units. The inner cavity of cyclodextrins is noted for its ability to form stable inclusion complexes with a wide variety of guests. A cyclodextrin-glucose host-guest complex was prepared and utilized as both a salt reductant and a particle stabilizer in the generation of aqueous metal colloids including Ag, Au, Pd, and Pt. The resulting colloids demonstrated remarkable stability---3 years and running, in some cases---and have been evaluated for thermal conductivity. Evaluation of the reaction products when the complex is used to reduce Pd 2+ demonstrated a unique comproportionation reaction in which the guest undergoes a two electron oxidation to produce a Pd atom. The resulting atom reduces a neighboring Pd2+ ion to yield two Pd + ions. The monovalent species, in contrast to Pd2+, can then oxidize the host to form atoms which rapidly aggregate to yield particles. Highly stable, crystalline copper(II) oxide particles were prepared which can be isolated as a powder and redispursed in low dielectric media such as hydrocarbons or chloroform. Mass concentrations of up to 20% (1.65 M) were achieved in octane, dodecane, and eicosane and remained stable for at least ten days at room temperature as observed by visible spectroscopy. Quasi-spherical particle shape was observed with the largest fraction possessing a diameter of 9 nm and 90% of the population existing within the range of 5 to 15 nm. The colloidal systems were characterized using FAA, XRD, TEM, UV-Vis, DSC, and a simple device inspired by Newton's Law of cooling which was employed to measure cooling/heating rates. Thermodynamic measurements of sodium oleate-stabilized CuO particles suspended in dodecane and eicosane reveal a decrease in Cp, DeltaH fus , and cooling/heating rates of the resulting colloid with large increases in particle mass concentration. Irradiation with 350 nm photons of anhydrous, air-free octane or toluene solutions of copper(II) oleate

  6. Host-guest chemistry for tuning colloidal solubility, self-organization and photoconductivity of inorganic-capped nanocrystals

    NASA Astrophysics Data System (ADS)

    Bodnarchuk, Maryna I.; Yakunin, Sergii; Piveteau, Laura; Kovalenko, Maksym V.

    2015-12-01

    Colloidal inorganic nanocrystals (NCs), functionalized with inorganic capping ligands, such as metal chalcogenide complexes (MCCs), have recently emerged as versatile optoelectronic materials. As-prepared, highly charged MCC-capped NCs are dispersible only in highly polar solvents, and lack the ability to form long-range ordered NC superlattices. Here we report a simple and general methodology, based on host-guest coordination of MCC-capped NCs with macrocyclic ethers (crown ethers and cryptands), enabling the solubilization of inorganic-capped NCs in solvents of any polarity and improving the ability to form NC superlattices. The corona of organic molecules can also serve as a convenient knob for the fine adjustment of charge transport and photoconductivity in films of NCs. In particular, high-infrared-photon detectivities of up to 3.3 × 1011 Jones with a fast response (3 dB cut-off at 3 kHz) at the wavelength of 1,200 nm were obtained with films of PbS/K3AsS4/decyl-18-crown-6 NCs.

  7. Host–guest chemistry for tuning colloidal solubility, self-organization and photoconductivity of inorganic-capped nanocrystals

    PubMed Central

    Bodnarchuk, Maryna I.; Yakunin, Sergii; Piveteau, Laura; Kovalenko, Maksym V.

    2015-01-01

    Colloidal inorganic nanocrystals (NCs), functionalized with inorganic capping ligands, such as metal chalcogenide complexes (MCCs), have recently emerged as versatile optoelectronic materials. As-prepared, highly charged MCC-capped NCs are dispersible only in highly polar solvents, and lack the ability to form long-range ordered NC superlattices. Here we report a simple and general methodology, based on host–guest coordination of MCC-capped NCs with macrocyclic ethers (crown ethers and cryptands), enabling the solubilization of inorganic-capped NCs in solvents of any polarity and improving the ability to form NC superlattices. The corona of organic molecules can also serve as a convenient knob for the fine adjustment of charge transport and photoconductivity in films of NCs. In particular, high-infrared-photon detectivities of up to 3.3 × 1011 Jones with a fast response (3 dB cut-off at 3 kHz) at the wavelength of 1,200 nm were obtained with films of PbS/K3AsS4/decyl-18-crown-6 NCs. PMID:26647828

  8. Colloidal Phenomena.

    ERIC Educational Resources Information Center

    Russel, William B.; And Others

    1979-01-01

    Described is a graduate level engineering course offered at Princeton University in colloidal phenomena stressing the physical and dynamical side of colloid science. The course outline, reading list, and requirements are presented. (BT)

  9. EDITORIAL: Colloidal suspensions Colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Petukhov, Andrei; Kegel, Willem; van Duijneveldt, Jeroen

    2011-05-01

    Special issue in honour of Henk Lekkerkerker's 65th birthday Professor Henk N W Lekkerkerker is a world-leading authority in the field of experimental and theoretical soft condensed matter. On the occasion of his 65th birthday in the summer of 2011, this special issue celebrates his many contributions to science. Henk Lekkerkerker obtained his undergraduate degree in chemistry at the University of Utrecht (1968) and moved to Calgary where he received his PhD in 1971. He moved to Brussels as a NATO fellow at the Université Libre de Bruxelles and was appointed to an assistant professorship (1974), an associate professorship (1977) and a full professorship (1980) in physical chemistry at the Vrije Universiteit Brussel. In 1985 he returned to The Netherlands to take up a professorship at the Van 't Hoff Laboratory, where he has been ever since. He has received a series of awards during his career, including the Onsager Medal (1999) of the University of Trondheim, the Bakhuys Roozeboom Gold Medal (2003) of the Royal Dutch Academy of Arts and Sciences (KNAW), the ECIS-Rhodia European Colloid and Interface Prize (2003), and the Liquid Matter Prize of the European Physical Society (2008). He was elected a member of KNAW in 1996, was awarded an Academy Chair position in 2005, and has held several visiting lectureships. Henk's work focuses on phase transitions in soft condensed matter, and he has made seminal contributions to both the theoretical and experimental aspects of this field. Here we highlight three major themes running through his work, and a few selected publications. So-called depletion interactions may lead to phase separation in colloid-polymer mixtures, and Henk realised that the partitioning of polymer needs to be taken into account to describe the phase behaviour correctly [1]. Colloidal suspensions can be used as model fluids, with the time- and length-scales involved leading to novel opportunities, notably the direct observation of capillary waves at a

  10. EDITORIAL: Colloidal suspensions Colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Petukhov, Andrei; Kegel, Willem; van Duijneveldt, Jeroen

    2011-05-01

    Special issue in honour of Henk Lekkerkerker's 65th birthday Professor Henk N W Lekkerkerker is a world-leading authority in the field of experimental and theoretical soft condensed matter. On the occasion of his 65th birthday in the summer of 2011, this special issue celebrates his many contributions to science. Henk Lekkerkerker obtained his undergraduate degree in chemistry at the University of Utrecht (1968) and moved to Calgary where he received his PhD in 1971. He moved to Brussels as a NATO fellow at the Université Libre de Bruxelles and was appointed to an assistant professorship (1974), an associate professorship (1977) and a full professorship (1980) in physical chemistry at the Vrije Universiteit Brussel. In 1985 he returned to The Netherlands to take up a professorship at the Van 't Hoff Laboratory, where he has been ever since. He has received a series of awards during his career, including the Onsager Medal (1999) of the University of Trondheim, the Bakhuys Roozeboom Gold Medal (2003) of the Royal Dutch Academy of Arts and Sciences (KNAW), the ECIS-Rhodia European Colloid and Interface Prize (2003), and the Liquid Matter Prize of the European Physical Society (2008). He was elected a member of KNAW in 1996, was awarded an Academy Chair position in 2005, and has held several visiting lectureships. Henk's work focuses on phase transitions in soft condensed matter, and he has made seminal contributions to both the theoretical and experimental aspects of this field. Here we highlight three major themes running through his work, and a few selected publications. So-called depletion interactions may lead to phase separation in colloid-polymer mixtures, and Henk realised that the partitioning of polymer needs to be taken into account to describe the phase behaviour correctly [1]. Colloidal suspensions can be used as model fluids, with the time- and length-scales involved leading to novel opportunities, notably the direct observation of capillary waves at a

  11. Chemistry and stability of thiol based polyethylene glycol surface coatings on colloidal gold and their relationship to protein adsorption and clearance in vivo

    NASA Astrophysics Data System (ADS)

    Carpinone, Paul

    Nanomaterials have presented a wide range of novel biomedical applications, with particular emphasis placed on advances in imaging and treatment delivery. Of the many particulate nanomaterials researched for biomedical applications, gold is one of the most widely used. Colloidal gold has been of great interest due to its chemical inertness and its ability to perform multiple functions, such as drug delivery, localized heating of tissues (hyperthermia), and imaging (as a contrast agent). It is also readily functionalized through the use of thiols, which spontaneously form sulfur to gold bonds with the surface. Polyethylene glycol (PEG) is the most widely used coating material for these particles as it provides both steric stability to the suspension and protein resistance. These properties extend the circulation time of the particles in blood, and consequently the efficacy of the treatment. Despite widespread use of PEG coated gold particles, the coating chemistry and stability of these particles are largely unknown. The goal of this work was to identify the mechanisms leading to degradation and stability of thiol based polyethylene glycol coatings on gold particles and to relate this behavior to protein adsorption and clearance in vivo. The results indicate that the protective PEG coating is susceptible to sources of oxidation (including dissolved oxygen) and competing adsorbates, among other factors. The quality of commercially available thiolated PEG reagents was also found to play a key role in the quality and protein resistance of the final PEG coating. Analysis of the stability of these coatings indicated that they rapidly degrade under physiological conditions, leading to the onset of protein adsorption when exposed to plasma or blood. Paralleling the protein adsorption behavior and onset of coating degradation observed in vitro, blood clearance of parenterally administered PEG coated particles in mice began after approximately 2h of circulation time. Taken

  12. Synthesis and Characterization of Supramolecular Colloids.

    PubMed

    Vilanova, Neus; De Feijter, Isja; Voets, Ilja K

    2016-01-01

    Control over colloidal assembly is of utmost importance for the development of functional colloidal materials with tailored structural and mechanical properties for applications in photonics, drug delivery and coating technology. Here we present a new family of colloidal building blocks, coined supramolecular colloids, whose self-assembly is controlled through surface-functionalization with a benzene-1,3,5-tricarboxamide (BTA) derived supramolecular moiety. Such BTAs interact via directional, strong, yet reversible hydrogen-bonds with other identical BTAs. Herein, a protocol is presented that describes how to couple these BTAs to colloids and how to quantify the number of coupling sites, which determines the multivalency of the supramolecular colloids. Light scattering measurements show that the refractive index of the colloids is almost matched with that of the solvent, which strongly reduces the van der Waals forces between the colloids. Before photo-activation, the colloids remain well dispersed, as the BTAs are equipped with a photo-labile group that blocks the formation of hydrogen-bonds. Controlled deprotection with UV-light activates the short-range hydrogen-bonds between the BTAs, which triggers the colloidal self-assembly. The evolution from the dispersed state to the clustered state is monitored by confocal microscopy. These results are further quantified by image analysis with simple routines using ImageJ and Matlab. This merger of supramolecular chemistry and colloidal science offers a direct route towards light- and thermo-responsive colloidal assembly encoded in the surface-grafted monolayer. PMID:27168201

  13. Hexadecapolar colloids

    PubMed Central

    Senyuk, Bohdan; Puls, Owen; Tovkach, Oleh M.; Chernyshuk, Stanislav B.; Smalyukh, Ivan I.

    2016-01-01

    Outermost occupied electron shells of chemical elements can have symmetries resembling that of monopoles, dipoles, quadrupoles and octupoles corresponding to filled s-, p-, d- and f-orbitals. Theoretically, elements with hexadecapolar outer shells could also exist, but none of the known elements have filled g-orbitals. On the other hand, the research paradigm of ‘colloidal atoms' displays complexity of particle behaviour exceeding that of atomic counterparts, which is driven by DNA functionalization, geometric shape and topology and weak external stimuli. Here we describe elastic hexadecapoles formed by polymer microspheres dispersed in a liquid crystal, a nematic fluid of orientationally ordered molecular rods. Because of conically degenerate boundary conditions, the solid microspheres locally perturb the alignment of the nematic host, inducing hexadecapolar distortions that drive anisotropic colloidal interactions. We uncover physical underpinnings of formation of colloidal elastic hexadecapoles and describe the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously. PMID:26864184

  14. Colloidal polypyrrole

    DOEpatents

    Armes, Steven P.; Aldissi, Mahmoud

    1990-01-01

    Processable electrically conductive latex polymer compositions including colloidal particles of an oxidized, polymerized aromatic heterocyclic monomer, a stabilizing effective amount of a vinyl pyridine-containing polymer and dopant anions and a method of preparing such polymer compositions are disclosed.

  15. Hexadecapolar colloids

    NASA Astrophysics Data System (ADS)

    Senyuk, Bohdan; Puls, Owen; Tovkach, Oleh M.; Chernyshuk, Stanislav B.; Smalyukh, Ivan I.

    2016-02-01

    Outermost occupied electron shells of chemical elements can have symmetries resembling that of monopoles, dipoles, quadrupoles and octupoles corresponding to filled s-, p-, d- and f-orbitals. Theoretically, elements with hexadecapolar outer shells could also exist, but none of the known elements have filled g-orbitals. On the other hand, the research paradigm of `colloidal atoms' displays complexity of particle behaviour exceeding that of atomic counterparts, which is driven by DNA functionalization, geometric shape and topology and weak external stimuli. Here we describe elastic hexadecapoles formed by polymer microspheres dispersed in a liquid crystal, a nematic fluid of orientationally ordered molecular rods. Because of conically degenerate boundary conditions, the solid microspheres locally perturb the alignment of the nematic host, inducing hexadecapolar distortions that drive anisotropic colloidal interactions. We uncover physical underpinnings of formation of colloidal elastic hexadecapoles and describe the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously.

  16. Hexadecapolar colloids.

    PubMed

    Senyuk, Bohdan; Puls, Owen; Tovkach, Oleh M; Chernyshuk, Stanislav B; Smalyukh, Ivan I

    2016-01-01

    Outermost occupied electron shells of chemical elements can have symmetries resembling that of monopoles, dipoles, quadrupoles and octupoles corresponding to filled s-, p-, d- and f-orbitals. Theoretically, elements with hexadecapolar outer shells could also exist, but none of the known elements have filled g-orbitals. On the other hand, the research paradigm of 'colloidal atoms' displays complexity of particle behaviour exceeding that of atomic counterparts, which is driven by DNA functionalization, geometric shape and topology and weak external stimuli. Here we describe elastic hexadecapoles formed by polymer microspheres dispersed in a liquid crystal, a nematic fluid of orientationally ordered molecular rods. Because of conically degenerate boundary conditions, the solid microspheres locally perturb the alignment of the nematic host, inducing hexadecapolar distortions that drive anisotropic colloidal interactions. We uncover physical underpinnings of formation of colloidal elastic hexadecapoles and describe the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously. PMID:26864184

  17. Hexadecapolar Colloids

    DOE PAGESBeta

    Senyuk, Bohdan; Puls, Owen; Tovkach, Oleh M.; Chernyshuk, Stanislav B.; Smalyukh, Ivan I.

    2016-02-11

    Outermost occupied electron shells of chemical elements can have symmetries resembling that of monopoles, dipoles, quadrupoles and octupoles corresponding to filled s-, p-, d- and forbitals. Theoretically, elements with hexadecapolar outer shells could also exist, but none of the known elements have filled g-orbitals. On the other hand, the research paradigm of ‘colloidal atoms’ displays complexity of particle behaviour exceeding that of atomic counterparts, which is driven by DNA functionalization, geometric shape and topology and weak external stimuli. We describe elastic hexadecapoles formed by polymer microspheres dispersed in a liquid crystal, a nematic fluid of orientationally ordered molecular rods. Becausemore » of conically degenerate boundary conditions, the solid microspheres locally perturb the alignment of the nematic host, inducing hexadecapolar distortions that drive anisotropic colloidal interactions. We uncover physical underpinnings of formation of colloidal elastic hexadecapoles and report the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously.« less

  18. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1983

    1983-01-01

    Presents chemistry experiments, laboratory procedures, demonstrations, and classroom materials/activities. These include: experiments on colloids, processing of uranium ore, action of heat on carbonates; color test for phenols and aromatic amines; solvent properties of non-electrolytes; stereoscopic applications/methods; a valency balance;…

  19. Topological colloids.

    PubMed

    Senyuk, Bohdan; Liu, Qingkun; He, Sailing; Kamien, Randall D; Kusner, Robert B; Lubensky, Tom C; Smalyukh, Ivan I

    2013-01-10

    Smoke, fog, jelly, paints, milk and shaving cream are common everyday examples of colloids, a type of soft matter consisting of tiny particles dispersed in chemically distinct host media. Being abundant in nature, colloids also find increasingly important applications in science and technology, ranging from direct probing of kinetics in crystals and glasses to fabrication of third-generation quantum-dot solar cells. Because naturally occurring colloids have a shape that is typically determined by minimization of interfacial tension (for example, during phase separation) or faceted crystal growth, their surfaces tend to have minimum-area spherical or topologically equivalent shapes such as prisms and irregular grains (all continuously deformable--homeomorphic--to spheres). Although toroidal DNA condensates and vesicles with different numbers of handles can exist and soft matter defects can be shaped as rings and knots, the role of particle topology in colloidal systems remains unexplored. Here we fabricate and study colloidal particles with different numbers of handles and genus g ranging from 1 to 5. When introduced into a nematic liquid crystal--a fluid made of rod-like molecules that spontaneously align along the so-called 'director'--these particles induce three-dimensional director fields and topological defects dictated by colloidal topology. Whereas electric fields, photothermal melting and laser tweezing cause transformations between configurations of particle-induced structures, three-dimensional nonlinear optical imaging reveals that topological charge is conserved and that the total charge of particle-induced defects always obeys predictions of the Gauss-Bonnet and Poincaré-Hopf index theorems. This allows us to establish and experimentally test the procedure for assignment and summation of topological charges in three-dimensional director fields. Our findings lay the groundwork for new applications of colloids and liquid crystals that range from

  20. Colloidal polyaniline

    DOEpatents

    Armes, Steven P.; Aldissi, Mahmoud

    1990-01-01

    Processable electrically conductive latex polymer compositions including colloidal particles of an oxidized, polymerized amino-substituted aromatic monomer, a stabilizing effective amount of a random copolymer containing amino-benzene type moieties as side chain constituents, and dopant anions, and a method of preparing such polymer compositions are provided.

  1. Mechanical Failure in Colloidal Gels

    NASA Astrophysics Data System (ADS)

    Kodger, Thomas Edward

    When colloidal particles in a dispersion are made attractive, they aggregate into fractal clusters which grow to form a space-spanning network, or gel, even at low volume fractions. These gels are crucial to the rheological behavior of many personal care, food products and dispersion-based paints. The mechanical stability of these products relies on the stability of the colloidal gel network which acts as a scaffold to provide these products with desired mechanical properties and to prevent gravitational sedimentation of the dispersed components. Understanding the mechanical stability of such colloidal gels is thus of crucial importance to predict and control the properties of many soft solids. Once a colloidal gel forms, the heterogeneous structure bonded through weak physical interactions, is immediately subject to body forces, such as gravity, surface forces, such as adhesion to a container walls and shear forces; the interplay of these forces acting on the gel determines its stability. Even in the absence of external stresses, colloidal gels undergo internal rearrangements within the network that may cause the network structure to evolve gradually, in processes known as aging or coarsening or fail catastrophically, in a mechanical instability known as syneresis. Studying gel stability in the laboratory requires model colloidal system which may be tuned to eliminate these body or endogenous forces systematically. Using existing chemistry, I developed several systems to study delayed yielding by eliminating gravitational stresses through density matching and cyclic heating to induce attraction; and to study syneresis by eliminating adhesion to the container walls, altering the contact forces between colloids, and again, inducing gelation through heating. These results elucidate the varied yet concomitant mechanisms by which colloidal gels may locally or globally yield, but then reform due to the nature of the physical, or non-covalent, interactions which form

  2. Soil colloidal behavior

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Recent understanding that organic and inorganic contaminants are often transported via colloidal particles has increased interest in colloid science. The primary importance of colloids in soil science stems from their surface reactivity and charge characteristics. Characterizations of size, shape,...

  3. Colloid Bound Transport of Contaminats In The Unsaturated Zone

    NASA Astrophysics Data System (ADS)

    Hofmann, T.; Christ, A.

    Colloids can play a major role in the relocation of contaminants in the unsaturated zone. The amount of colloid driven transport is defined by soil chemistry, soil water chemistry and water flow velocity as well as colloid composition and formation. In a current research project we investigate the filtration and mobilization of colloids in unsaturated column studies. We use different soil types, chosen by a wide range of mean grain size and heterogeneity. Particle tracers are polystyrene solids with a de- fined negative surface charge and defined size from 50 nm to 10 µm. In addition, we use natural colloids extracted from a wide range of contaminated and uncontaminated land. Experimental conditions are exactly controlled throughout all the time. We alter mainly flow velocity ionic strength in order to study the filtration behaviour of the soils. In addition, Pyrene and Lead are are used as model contaminants. First results show the colloids are not retarded in many coarse structured soil types. Preferential colloid flow shows a major impact in breakthrough behaviour. Colloid bound lead is relocated significant through the unsaturated zone, whereas non colloid bound lead species are strongly retarded. In the presentation we will show results of contami- nant processes and present new results on the filtration behaviour of colloids in the unsaturated zone depending on flow velocity, soil type and colloid size.

  4. Colloidal characterization of silicon nitride and silicon carbide

    NASA Technical Reports Server (NTRS)

    Feke, Donald L.

    1986-01-01

    The colloidal behavior of aqueous ceramic slips strongly affects the forming and sintering behavior and the ultimate mechanical strength of the final ceramic product. The colloidal behavior of these materials, which is dominated by electrical interactions between the particles, is complex due to the strong interaction of the solids with the processing fluids. A surface titration methodology, modified to account for this interaction, was developed and used to provide fundamental insights into the interfacial chemistry of these systems. Various powder pretreatment strategies were explored to differentiate between true surface chemistry and artifacts due to exposure history. The colloidal behavior of both silicon nitride and carbide is dominated by silanol groups on the powder surfaces. However, the colloid chemistry of silicon nitride is apparently influenced by an additional amine group. With the proper powder treatments, silicon nitride and carbide powder can be made to appear colloidally equivalent. The impact of these results on processing control will be discussed.

  5. Colloidal Dispersions

    NASA Astrophysics Data System (ADS)

    Russel, W. B.; Saville, D. A.; Schowalter, W. R.

    1992-03-01

    The book covers the physical side of colloid science from the individual forces acting between submicron particles suspended in a liquid through the resulting equilibrium and dynamic properties. The relevant forces include Brownian motion, electrostatic repulsion, dispersion attraction, both attraction and repulsion due to soluble polymer, and viscous forces due to relative motion between the particles and the liquid. The balance among Brownian motion and the interparticle forces decides the questions of stability and phase behavior. Imposition of external fields produces complex effects, i.e. electrokinetic phenomena (electric field), sedimentation (gravitational field), diffusion (concentration/chemical potential gradient), and non-Newtonian rheology (shear field). The treatment aims to impart a sound, quantitative understanding based on fundamental theory and experiments with well-characterized model systems. This broad grasp of the fundamentals lends insight and helps to develop the intuitive sense needed to isolate essential features of technological problems and design critical experiments. Some exposure to fluid mechanics, statistical mechanics, and electricity and magnetism is assumed, but each subject is reintroduced in a self-contained manner.

  6. Manipulation of gold colloidal nanoparticles with atomic force microscopy in dynamic mode: influence of particle–substrate chemistry and morphology, and of operating conditions

    PubMed Central

    Darwich, Samer; Rao, Akshata; Gnecco, Enrico; Jayaraman, Shrisudersan; Haidara, Hamidou

    2011-01-01

    Summary One key component in the assembly of nanoparticles is their precise positioning to enable the creation of new complex nano-objects. Controlling the nanoscale interactions is crucial for the prediction and understanding of the behaviour of nanoparticles (NPs) during their assembly. In the present work, we have manipulated bare and functionalized gold nanoparticles on flat and patterned silicon and silicon coated substrates with dynamic atomic force microscopy (AFM). Under ambient conditions, the particles adhere to silicon until a critical drive amplitude is reached by oscillations of the probing tip. Beyond that threshold, the particles start to follow different directions, depending on their geometry, size and adhesion to the substrate. Higher and respectively, lower mobility was observed when the gold particles were coated with methyl (–CH3) and hydroxyl (–OH) terminated thiol groups. This major result suggests that the adhesion of the particles to the substrate is strongly reduced by the presence of hydrophobic interfaces. The influence of critical parameters on the manipulation was investigated and discussed viz. the shape, size and grafting of the NPs, as well as the surface chemistry and the patterning of the substrate, and finally the operating conditions (temperature, humidity and scan velocity). Whereas the operating conditions and substrate structure are shown to have a strong effect on the mobility of the particles, we did not find any differences when manipulating ordered vs random distributed particles. PMID:21977418

  7. Manipulation of gold colloidal nanoparticles with atomic force microscopy in dynamic mode: influence of particle-substrate chemistry and morphology, and of operating conditions.

    PubMed

    Darwich, Samer; Mougin, Karine; Rao, Akshata; Gnecco, Enrico; Jayaraman, Shrisudersan; Haidara, Hamidou

    2011-01-01

    One key component in the assembly of nanoparticles is their precise positioning to enable the creation of new complex nano-objects. Controlling the nanoscale interactions is crucial for the prediction and understanding of the behaviour of nanoparticles (NPs) during their assembly. In the present work, we have manipulated bare and functionalized gold nanoparticles on flat and patterned silicon and silicon coated substrates with dynamic atomic force microscopy (AFM). Under ambient conditions, the particles adhere to silicon until a critical drive amplitude is reached by oscillations of the probing tip. Beyond that threshold, the particles start to follow different directions, depending on their geometry, size and adhesion to the substrate. Higher and respectively, lower mobility was observed when the gold particles were coated with methyl (-CH(3)) and hydroxyl (-OH) terminated thiol groups. This major result suggests that the adhesion of the particles to the substrate is strongly reduced by the presence of hydrophobic interfaces. The influence of critical parameters on the manipulation was investigated and discussed viz. the shape, size and grafting of the NPs, as well as the surface chemistry and the patterning of the substrate, and finally the operating conditions (temperature, humidity and scan velocity). Whereas the operating conditions and substrate structure are shown to have a strong effect on the mobility of the particles, we did not find any differences when manipulating ordered vs random distributed particles. PMID:21977418

  8. Colloidal Silver Products

    MedlinePlus

    ... can be dangerous to your health. What the Science Says About the Safety and Side Effects of ... homemade and commercial colloidal silver products. What the Science Says About the Effectiveness of Colloidal Silver Scientific ...

  9. What Is a Colloid?

    ERIC Educational Resources Information Center

    Lamb, William G.

    1985-01-01

    Describes the properties of colloids, listing those commonly encountered (such as whipped cream, mayonnaise, and fog). Also presents several experiments using colloids and discusses "Silly Putty," a colloid with viscoelastic properties whose counterintuitive properties result from its mixture of polymers. (DH)

  10. Electrohydrodynamically patterned colloidal crystals

    NASA Technical Reports Server (NTRS)

    Hayward, Ryan C. (Inventor); Poon, Hak F. (Inventor); Xiao, Yi (Inventor); Saville, Dudley A. (Inventor); Aksay, Ilhan A. (Inventor)

    2003-01-01

    A method for assembling patterned crystalline arrays of colloidal particles using ultraviolet illumination of an optically-sensitive semiconducting anode while using the anode to apply an electronic field to the colloidal particles. The ultraviolet illumination increases current density, and consequently, the flow of the colloidal particles. As a result, colloidal particles can be caused to migrate from non-illuminated areas of the anode to illuminated areas of the anode. Selective illumination of the anode can also be used to permanently affix colloidal crystals to illuminated areas of the anode while not affixing them to non-illuminated areas of the anode.

  11. Microfluidic colloid filtration

    PubMed Central

    Linkhorst, John; Beckmann, Torsten; Go, Dennis; Kuehne, Alexander J. C.; Wessling, Matthias

    2016-01-01

    Filtration of natural and colloidal matter is an essential process in today’s water treatment processes. The colloidal matter is retained with the help of micro- and nanoporous synthetic membranes. Colloids are retained in a “cake layer” – often coined fouling layer. Membrane fouling is the most substantial problem in membrane filtration: colloidal and natural matter build-up leads to an increasing resistance and thus decreasing water transport rate through the membrane. Theoretical models exist to describe macroscopically the hydrodynamic resistance of such transport and rejection phenomena; however, visualization of the various phenomena occurring during colloid retention is extremely demanding. Here we present a microfluidics based methodology to follow filter cake build up as well as transport phenomena occuring inside of the fouling layer. The microfluidic colloidal filtration methodology enables the study of complex colloidal jamming, crystallization and melting processes as well as translocation at the single particle level. PMID:26927706

  12. Saturated Zone Colloid Transport

    SciTech Connect

    H. Viswanathan; P. Reimus

    2003-09-05

    Colloid retardation is influenced by the attachment and detachment of colloids from immobile surfaces. This analysis demonstrates the development of parameters necessary to estimate attachment and detachment of colloids and, hence, retardation in both fractured tuff and porous alluvium. Field and experimental data specific to fractured tuff are used for the analysis of colloid retardation in fractured tuff. Experimental data specific to colloid transport in alluvial material from Yucca Mountain as well as bacteriophage field studies in alluvial material, which are thought to be good analogs for colloid transport, are used to estimate attachment and detachment of colloids in the alluvial material. There are no alternative scientific approaches or technical methods for calculating these retardation factors.

  13. Microfluidic colloid filtration.

    PubMed

    Linkhorst, John; Beckmann, Torsten; Go, Dennis; Kuehne, Alexander J C; Wessling, Matthias

    2016-01-01

    Filtration of natural and colloidal matter is an essential process in today's water treatment processes. The colloidal matter is retained with the help of micro- and nanoporous synthetic membranes. Colloids are retained in a "cake layer" - often coined fouling layer. Membrane fouling is the most substantial problem in membrane filtration: colloidal and natural matter build-up leads to an increasing resistance and thus decreasing water transport rate through the membrane. Theoretical models exist to describe macroscopically the hydrodynamic resistance of such transport and rejection phenomena; however, visualization of the various phenomena occurring during colloid retention is extremely demanding. Here we present a microfluidics based methodology to follow filter cake build up as well as transport phenomena occuring inside of the fouling layer. The microfluidic colloidal filtration methodology enables the study of complex colloidal jamming, crystallization and melting processes as well as translocation at the single particle level. PMID:26927706

  14. Microfluidic colloid filtration

    NASA Astrophysics Data System (ADS)

    Linkhorst, John; Beckmann, Torsten; Go, Dennis; Kuehne, Alexander J. C.; Wessling, Matthias

    2016-03-01

    Filtration of natural and colloidal matter is an essential process in today’s water treatment processes. The colloidal matter is retained with the help of micro- and nanoporous synthetic membranes. Colloids are retained in a “cake layer” - often coined fouling layer. Membrane fouling is the most substantial problem in membrane filtration: colloidal and natural matter build-up leads to an increasing resistance and thus decreasing water transport rate through the membrane. Theoretical models exist to describe macroscopically the hydrodynamic resistance of such transport and rejection phenomena; however, visualization of the various phenomena occurring during colloid retention is extremely demanding. Here we present a microfluidics based methodology to follow filter cake build up as well as transport phenomena occuring inside of the fouling layer. The microfluidic colloidal filtration methodology enables the study of complex colloidal jamming, crystallization and melting processes as well as translocation at the single particle level.

  15. Getting Reactions to Chemistry.

    ERIC Educational Resources Information Center

    Smith, Walter S.

    1983-01-01

    "COMETS on Careers" describes science-related careers, introduces activities illustrating a science concept being studied, and encourages use of professional persons as activity leaders. Several COMETS chemistry activities are described. These activities, which can be performed in school or at home, focus on colloids, acid/base indicators, and…

  16. Saturated Zone Colloid Transport

    SciTech Connect

    H. S. Viswanathan

    2004-10-07

    This scientific analysis provides retardation factors for colloids transporting in the saturated zone (SZ) and the unsaturated zone (UZ). These retardation factors represent the reversible chemical and physical filtration of colloids in the SZ. The value of the colloid retardation factor, R{sub col} is dependent on several factors, such as colloid size, colloid type, and geochemical conditions (e.g., pH, Eh, and ionic strength). These factors are folded into the distributions of R{sub col} that have been developed from field and experimental data collected under varying geochemical conditions with different colloid types and sizes. Attachment rate constants, k{sub att}, and detachment rate constants, k{sub det}, of colloids to the fracture surface have been measured for the fractured volcanics, and separate R{sub col} uncertainty distributions have been developed for attachment and detachment to clastic material and mineral grains in the alluvium. Radionuclides such as plutonium and americium sorb mostly (90 to 99 percent) irreversibly to colloids (BSC 2004 [DIRS 170025], Section 6.3.3.2). The colloid retardation factors developed in this analysis are needed to simulate the transport of radionuclides that are irreversibly sorbed onto colloids; this transport is discussed in the model report ''Site-Scale Saturated Zone Transport'' (BSC 2004 [DIRS 170036]). Although it is not exclusive to any particular radionuclide release scenario, this scientific analysis especially addresses those scenarios pertaining to evidence from waste-degradation experiments, which indicate that plutonium and americium may be irreversibly attached to colloids for the time scales of interest. A section of this report will also discuss the validity of using microspheres as analogs to colloids in some of the lab and field experiments used to obtain the colloid retardation factors. In addition, a small fraction of colloids travels with the groundwater without any significant retardation

  17. Ring around the colloid

    NASA Astrophysics Data System (ADS)

    Cavallaro, Marcello, Jr.; Gharbi, Mohamed A.; Beller, Daniel A.; Čopar, Simon; Shi, Zheng; Kamien, Randall D.; Yang, Shu; Baumgart, Tobias; Stebe, Kathleen J.

    In this work, we show that Janus washers, genus-one colloids with hybrid anchoring conditions, form topologically required defects in nematic liquid crystals. Experiments under crossed polarizers reveal the defect structure to be a rigid disclination loop confined within the colloid, with an accompanying defect in the liquid crystal. When confined to a homeotropic cell, the resulting colloid-defect ring pair tilts relative to the far field director, in contrast to the behavior of toroidal colloids with purely homeotropic anchoring. We show that this tilting behavior can be reversibly suppressed by the introduction of a spherical colloid into the center of the toroid, creating a new kind of multi-shape colloidal assemblage.

  18. Bulk synthesis of polymer-inorganic colloidal clusters.

    PubMed

    Perro, Adeline; Manoharan, Vinothan N

    2010-12-21

    We describe a procedure to synthesize colloidal clusters with polyhedral morphologies in high yield (liter quantities at up to 70% purity) using a combination of emulsion polymerization and inorganic surface chemistry. We show that the synthesis initially used for silica-polystyrene hybrid clusters can be generalized to create clusters from other inorganic and polymer particles. We also show that high yields of particular morphologies can be obtained by precise control of the inorganic seed particle size, a finding that can be explained using a hard-sphere packing model. These clusters can be further chemically modified for a variety of applications. Introducing a cross-linker leads to colloidal clusters that can be index matched in an appropriate solvent, allowing them to be used for particle tracking or optical studies of colloidal self-assembly. Also, depositing a thin silica layer on these colloids allows the surface properties to be controlled using silane chemistry. PMID:21080658

  19. UZ Colloid Transport Model

    SciTech Connect

    M. McGraw

    2000-04-13

    The UZ Colloid Transport model development plan states that the objective of this Analysis/Model Report (AMR) is to document the development of a model for simulating unsaturated colloid transport. This objective includes the following: (1) use of a process level model to evaluate the potential mechanisms for colloid transport at Yucca Mountain; (2) Provide ranges of parameters for significant colloid transport processes to Performance Assessment (PA) for the unsaturated zone (UZ); (3) Provide a basis for development of an abstracted model for use in PA calculations.

  20. Analysis of colloid transport

    SciTech Connect

    Travis, B.J.; Nuttall, H.E.

    1985-12-31

    The population balance methodology is described and applied to the transport and capture of polydispersed colloids in packed columns. The transient model includes particle growth, capture, convective transport, and dispersion. We also follow the dynamic accumulation of captured colloids on the solids. The multidimensional parabolic partial differential equation was solved by a recently enhanced method of characteristics technique. This computational technique minimized numerical dispersion and is computationally very fast. The FORTRAN 77 code ran on a VAX-780 in less than a minute and also runs on an IBM-AT using the Professional FORTRAN compiler. The code was extensively tested against various simplified cases and against analytical models. The packed column experiments by Saltelli et al. were re-analyzed incorporating the experimentally reported size distribution of the colloid feed material. Colloid capture was modeled using a linear size dependent filtration function. The effects of a colloid size dependent filtration factor and various initial colloid size distributions on colloid migration and capture were investigated. Also, we followed the changing colloid size distribution as a function of position in the column. Some simple arguments are made to assess the likelihood of colloid migration at a potential NTS Yucca Mountain waste disposal site. 10 refs., 3 figs., 1 tab.

  1. Modeling colloid transport for performance assessment.

    PubMed

    Contardi, J S; Turner, D R; Ahn, T M

    2001-02-01

    The natural system is expected to contribute to isolation at the proposed high-level nuclear waste (HLW) geologic repository at Yucca Mountain, NV (YM). In developing performance assessment (PA) computer models to simulate long-term behavior at YM, colloidal transport of radionuclides has been proposed as a critical factor because of the possible reduced interaction with the geologic media. Site-specific information on the chemistry and natural colloid concentration of saturated zone groundwaters in the vicinity of YM is combined with a surface complexation sorption model to evaluate the impact of natural colloids on calculated retardation factors (RF) for several radioelements of concern in PA. Inclusion of colloids into the conceptual model can reduce the calculated effective retardation significantly. Strongly sorbed radionuclides such as americium and thorium are most affected by pseudocolloid formation and transport, with a potential reduction in RF of several orders of magnitude. Radioelements that are less strongly sorbed under YM conditions, such as uranium and neptunium, are not affected significantly by colloid transport, and transport of plutonium in the valence state is only moderately enhanced. Model results showed no increase in the peak mean annual total effective dose equivalent (TEDE) within a compliance period of 10,000 years, although this is strongly dependent on container life in the base case scenario. At longer times, simulated container failures increase and the TEDE from the colloidal models increased by a factor of 60 from the base case. By using mechanistic models and sensitivity analyses to determine what parameters and transport processes affect the TEDE, colloidal transport in future versions of the TPA code can be represented more accurately. PMID:11288586

  2. Swelling-based method for preparing stable, functionalized polymer colloids.

    PubMed

    Kim, Anthony J; Manoharan, Vinothan N; Crocker, John C

    2005-02-16

    We describe a swelling-based method to prepare sterically stabilized polymer colloids with different functional groups or biomolecules attached to their surface. It should be applicable to a variety of polymeric colloids, including magnetic particles, fluorescent particles, polystyrene particles, PMMA particles, and so forth. The resulting particles are more stable in the presence of monovalent and divalent salt than existing functionalized colloids, even in the absence of any surfactant or protein blocker. While we use a PEG polymer brush here, the method should enable the use of a variety of polymer chemistries and molecular weights. PMID:15700965

  3. Interface colloidal robotic manipulator

    DOEpatents

    Aronson, Igor; Snezhko, Oleksiy

    2015-08-04

    A magnetic colloidal system confined at the interface between two immiscible liquids and energized by an alternating magnetic field dynamically self-assembles into localized asters and arrays of asters. The colloidal system exhibits locomotion and shape change. By controlling a small external magnetic field applied parallel to the interface, structures can capture, transport, and position target particles.

  4. Driving magnetic colloidal polymers

    NASA Astrophysics Data System (ADS)

    Dempster, Joshua; Olvera de La Cruz, Monica

    Magnetic colloids are of growing interest for applications such as drug delivery and in vitro tissue growth. Recent experiments have synthesized 1D chains of magnetic colloids into permanent colloidal polymers. We study magnetic colloidal polymers theoretically and computationally under the influence of time-varying external fields and find a rich set of controllable, dynamic conformations. By iterating through a sequence of conformations, these polymers can perform mechanical functions. We discuss possible roles for these polymers beyond those considered for single colloids. This work was supported as part of the Center for Bio-Inspired Energy Science, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under Award # DE-SC0000989.

  5. Assembly of Colloidal Materials Using Bioadhesive Interactions

    NASA Astrophysics Data System (ADS)

    Hammer, Daniel A.; Hiddessen, Amy L.; Tohver, Valeria; Crocker, John C.; Weitz, David A.

    2002-11-01

    We have pursued the use of biological crosslinking molecules of several types to make colloidal materials at relatively low volume fraction of colloidal particles. The objective is to make binary alloys of colloidal particles, made of two different colloidal particles coated with complementary biological lock-and-key binding molecules, which assemble due to the biological specificity. The long-term goal is to use low affinity lock-and-key biological interactions, so that the can anneal to form crystalline states. We have used a variety of different surface chemistries in order to make colloidal materials. Our first system involved using selectin-carbohydrate (sialyl-Lewis) interactions; this chemistry is derived from immune system. This chemical interaction is of relatively low affinity, with timescales for dissociation of several seconds. Furthermore, the adhesion mediated by these molecules can be reversed by the chelation of calcium atoms; thus assembled structures can be disassembled reversibly. Our second system employed avidin-biotin chemistry. This well-studied system is of high affinity, and is generally irreversible on a laboratory time-scale. Thus, we would expect selectin-carbohydrate interactions at high molecular density and avidin-biotin interactions to give kinetically-trapped structures; however, at low densities, we would expect significant differences in the structure and dynamics of the two materials, owing to their very different release rates. We have also begun to use a third chemistry - DNA hybridization. By attaching single stranded DNA oligonucleotide chains to beads, we can drive the assembly of colloidal materials by hybridization of complementary DNA chains. It is well known that DNA adenosine-thymine (A-T) and guanine-cytosine (G-C) bases hybridize pairwise with a Gibbs free energy change of 1.7 kcal/mol per base; thus, the energy of the assembly can be modulated by altering the number of complementary bases in the DNA chains. Using

  6. Assembly of Colloidal Materials Using Bioadhesive Interactions

    NASA Technical Reports Server (NTRS)

    Hammer, Daniel A.; Hiddessen, Amy L.; Tohver, Valeria; Crocker, John C.; Weitz, David A.

    2002-01-01

    We have pursued the use of biological crosslinking molecules of several types to make colloidal materials at relatively low volume fraction of colloidal particles. The objective is to make binary alloys of colloidal particles, made of two different colloidal particles coated with complementary biological lock-and-key binding molecules, which assemble due to the biological specificity. The long-term goal is to use low affinity lock-and-key biological interactions, so that the can anneal to form crystalline states. We have used a variety of different surface chemistries in order to make colloidal materials. Our first system involved using selectin-carbohydrate (sialyl-Lewis) interactions; this chemistry is derived from immune system. This chemical interaction is of relatively low affinity, with timescales for dissociation of several seconds. Furthermore, the adhesion mediated by these molecules can be reversed by the chelation of calcium atoms; thus assembled structures can be disassembled reversibly. Our second system employed avidin-biotin chemistry. This well-studied system is of high affinity, and is generally irreversible on a laboratory time-scale. Thus, we would expect selectin-carbohydrate interactions at high molecular density and avidin-biotin interactions to give kinetically-trapped structures; however, at low densities, we would expect significant differences in the structure and dynamics of the two materials, owing to their very different release rates. We have also begun to use a third chemistry - DNA hybridization. By attaching single stranded DNA oligonucleotide chains to beads, we can drive the assembly of colloidal materials by hybridization of complementary DNA chains. It is well known that DNA adenosine-thymine (A-T) and guanine-cytosine (G-C) bases hybridize pairwise with a Gibbs free energy change of 1.7 kcal/mol per base; thus, the energy of the assembly can be modulated by altering the number of complementary bases in the DNA chains. Using

  7. Lock and key colloids.

    PubMed

    Sacanna, S; Irvine, W T M; Chaikin, P M; Pine, D J

    2010-03-25

    New functional materials can in principle be created using colloids that self-assemble into a desired structure by means of a programmable recognition and binding scheme. This idea has been explored by attaching 'programmed' DNA strands to nanometre- and micrometre- sized particles and then using DNA hybridization to direct the placement of the particles in the final assembly. Here we demonstrate an alternative recognition mechanism for directing the assembly of composite structures, based on particles with complementary shapes. Our system, which uses Fischer's lock-and-key principle, employs colloidal spheres as keys and monodisperse colloidal particles with a spherical cavity as locks that bind spontaneously and reversibly via the depletion interaction. The lock-and-key binding is specific because it is controlled by how closely the size of a spherical colloidal key particle matches the radius of the spherical cavity of the lock particle. The strength of the binding can be further tuned by adjusting the solution composition or temperature. The composite assemblies have the unique feature of having flexible bonds, allowing us to produce flexible dimeric, trimeric and tetrameric colloidal molecules as well as more complex colloidal polymers. We expect that this lock-and-key recognition mechanism will find wider use as a means of programming and directing colloidal self-assembly. PMID:20336142

  8. Colloidal Synthesis of Gold Semishells

    PubMed Central

    Rodríguez-Fernández, Denis; Pérez-Juste, Jorge; Pastoriza-Santos, Isabel; Liz-Marzán, Luis M

    2012-01-01

    This work describes a novel and scalable colloid chemistry strategy to fabricate gold semishells based on the selective growth of gold on Janus silica particles (500 nm in diameter) partly functionalized with amino groups. The modulation of the geometry of the Janus silica particles allows us to tune the final morphology of the gold semishells. This method also provides a route to fabricating hollow gold semishells through etching of the silica cores with hydrofluoric acid. The optical properties were characterized by visible near-infrared (vis-NIR) spectroscopy and compared with simulations performed using the boundary element method (BEM). These revealed that the main optical features are located beyond the NIR region because of the large core size. PMID:24551496

  9. Practical colloidal processing of multication ceramics

    SciTech Connect

    Bell, Nelson S.; Monson, Todd C.; Diantonio, Christopher; Wu, Yiquan

    2015-09-07

    The use of colloidal processing principles in the formation of ceramic materials is well appreciated for developing homogeneous material properties in sintered products, enabling novel forming techniques for porous ceramics or 3D printing, and controlling microstructure to enable optimized material properties. The solution processing of electronic ceramic materials often involves multiple cationic elements or dopants to affect microstructure and properties. Material stability must be considered through the steps of colloidal processing to optimize desired component properties. This review provides strategies for preventing material degradation in particle synthesis, milling processes, and dispersion, with case studies of consolidation using spark plasma sintering of these systems. The prevention of multication corrosion in colloidal dispersions can be achieved by utilizing conditions similar to the synthesis environment or by the development of surface passivation layers. The choice of dispersing surfactants can be related to these surface states, which are of special importance for nanoparticle systems. A survey of dispersant chemistries related to some common synthesis conditions is provided for perovskite systems as an example. Furthermore, these principles can be applied to many colloidal systems related to electronic and optical applications.

  10. Practical colloidal processing of multication ceramics

    DOE PAGESBeta

    Bell, Nelson S.; Monson, Todd C.; Diantonio, Christopher; Wu, Yiquan

    2015-09-07

    The use of colloidal processing principles in the formation of ceramic materials is well appreciated for developing homogeneous material properties in sintered products, enabling novel forming techniques for porous ceramics or 3D printing, and controlling microstructure to enable optimized material properties. The solution processing of electronic ceramic materials often involves multiple cationic elements or dopants to affect microstructure and properties. Material stability must be considered through the steps of colloidal processing to optimize desired component properties. This review provides strategies for preventing material degradation in particle synthesis, milling processes, and dispersion, with case studies of consolidation using spark plasma sinteringmore » of these systems. The prevention of multication corrosion in colloidal dispersions can be achieved by utilizing conditions similar to the synthesis environment or by the development of surface passivation layers. The choice of dispersing surfactants can be related to these surface states, which are of special importance for nanoparticle systems. A survey of dispersant chemistries related to some common synthesis conditions is provided for perovskite systems as an example. Furthermore, these principles can be applied to many colloidal systems related to electronic and optical applications.« less

  11. Colloidal pen lithography.

    PubMed

    Xue, Mianqi; Cai, Xiaojing; Chen, Ghenfu

    2015-02-01

    Colloidal pen lithography, a low-cost, high-throughput scanning probe contact printing method, has been developed, which is based on self-assembled colloidal arrays embedded in a soft elastomeric stamp. Patterned protein arrays are demonstrated using this method, with a feature size ranging from 100 nm to several micrometers. A brief study into the specificity reorganization of protein gives evidence for the feasibility of this method for writing protein chips. PMID:25288364

  12. MOBILIZATION AND CHARACTERIZATION OF COLLOIDS GENERATED FROM CEMENT LEACHATES MOVING THROUGH A SRS SANDY SEDIMENT

    SciTech Connect

    Li, D.; Roberts, K.; Kaplan, D.; Seaman, J.

    2011-09-20

    Naturally occurring mobile colloids are ubiquitous and are involved in many important processes in the subsurface zone. For example, colloid generation and subsequent mobilization represent a possible mechanism for the transport of contaminants including radionuclides in the subsurface environments. For colloid-facilitated transport to be significant, three criteria must be met: (1) colloids must be generated; (2) contaminants must associate with the colloids preferentially to the immobile solid phase (aquifer); and (3) colloids must be transported through the groundwater or in subsurface environments - once these colloids start moving they become 'mobile colloids'. Although some experimental investigations of particle release in natural porous media have been conducted, the detailed mechanisms of release and re-deposition of colloidal particles within natural porous media are poorly understood. Even though this vector of transport is known, the extent of its importance is not known yet. Colloid-facilitated transport of trace radionuclides has been observed in the field, thus demonstrating a possible radiological risk associated with the colloids. The objective of this study was to determine if cementitious leachate would promote the in situ mobilization of natural colloidal particles from a SRS sandy sediment. The intent was to determine whether cementitious surface or subsurface structure would create plumes that could produce conditions conducive to sediment dispersion and mobile colloid generation. Column studies were conducted and the cation chemistries of influents and effluents were analyzed by ICP-OES, while the mobilized colloids were characterized using XRD, SEM, EDX, PSD and Zeta potential. The mobilization mechanisms of colloids in a SRS sandy sediment by cement leachates were studied.

  13. Design and synthesis of model transparent aqueous colloids with optimal scattering properties.

    PubMed

    Perro, Adeline; Meng, Guangnan; Fung, Jerome; Manoharan, Vinothan N

    2009-10-01

    We demonstrate the synthesis and self-assembly of colloidal particles with independently controlled diameter and scattering cross section. We show that it is possible to prepare bulk colloidal suspensions that are nearly transparent in water, while the particles themselves can be individually resolved using optical microscopy. These particles may be ideal model colloids for real-space studies of self-assembly in aqueous media. Moreover, they illustrate the degree to which the optical properties of colloids can be engineered through straightforward chemistry. PMID:19728724

  14. Spherical colloidal photonic crystals.

    PubMed

    Zhao, Yuanjin; Shang, Luoran; Cheng, Yao; Gu, Zhongze

    2014-12-16

    CONSPECTUS: Colloidal photonic crystals (PhCs), periodically arranged monodisperse nanoparticles, have emerged as one of the most promising materials for light manipulation because of their photonic band gaps (PBGs), which affect photons in a manner similar to the effect of semiconductor energy band gaps on electrons. The PBGs arise due to the periodic modulation of the refractive index between the building nanoparticles and the surrounding medium in space with subwavelength period. This leads to light with certain wavelengths or frequencies located in the PBG being prohibited from propagating. Because of this special property, the fabrication and application of colloidal PhCs have attracted increasing interest from researchers. The most simple and economical method for fabrication of colloidal PhCs is the bottom-up approach of nanoparticle self-assembly. Common colloidal PhCs from this approach in nature are gem opals, which are made from the ordered assembly and deposition of spherical silica nanoparticles after years of siliceous sedimentation and compression. Besides naturally occurring opals, a variety of manmade colloidal PhCs with thin film or bulk morphology have also been developed. In principle, because of the effect of Bragg diffraction, these PhC materials show different structural colors when observed from different angles, resulting in brilliant colors and important applications. However, this angle dependence is disadvantageous for the construction of some optical materials and devices in which wide viewing angles are desired. Recently, a series of colloidal PhC materials with spherical macroscopic morphology have been created. Because of their spherical symmetry, the PBGs of spherical colloidal PhCs are independent of rotation under illumination of the surface at a fixed incident angle of the light, broadening the perspective of their applications. Based on droplet templates containing colloidal nanoparticles, these spherical colloidal PhCs can be

  15. Natural analogue studies of the role of colloids, natural organics and microorganisms on radionuclide transport

    SciTech Connect

    McCarthy, J.F.

    1994-10-01

    Colloids may be important as a geochemical transport mechanism for radionuclides at geological repositories if they are (1) present in the groundwater, (2) stable with respect to both colloidal and chemical stabilities, (3) capable of adsorbing radionuclides, especially if the sorption is irreversible, and (4) mobile in the subsurface. The available evidence from natural analogue and other field studies relevant to these issues is reviewed, as is the potential role of mobile microorganisms ({open_quotes}biocolloids{close_quotes}) on radionuclide migration. Studies have demonstrated that colloids are ubiquitous in groundwater, although colloid concentrations in deep, geochemically stable systems may be too low to affect radionuclide transport. However, even low colloid populations cannot be dismissed as a potential concern because colloids appear to be stable, and many radionuclides that adsorb to colloids are not readily desorbed over long periods. Field studies offer somewhat equivocal evidence concerning colloid mobility and cannot prove or disprove the significance of colloid transport in the far-field environment. Additional research is needed at new sites to properly represent a repository far-field. Performance assessment would benefit from natural analogue studies to examine colloid behavior at sites encompassing a suite of probable groundwater chemistries and that mimic the types of formations selected for radioactive waste repositories.

  16. Colloidal characterization of ultrafine silicon carbide and silicon nitride powders

    NASA Technical Reports Server (NTRS)

    Whitman, Pamela K.; Feke, Donald L.

    1986-01-01

    The effects of various powder treatment strategies on the colloid chemistry of aqueous dispersions of silicon carbide and silicon nitride are examined using a surface titration methodology. Pretreatments are used to differentiate between the true surface chemistry of the powders and artifacts resulting from exposure history. Silicon nitride powders require more extensive pretreatment to reveal consistent surface chemistry than do silicon carbide powders. As measured by titration, the degree of proton adsorption from the suspending fluid by pretreated silicon nitride and silicon carbide powders can both be made similar to that of silica.

  17. Self-assembly of active colloidal molecules with dynamic function

    NASA Astrophysics Data System (ADS)

    Soto, Rodrigo; Golestanian, Ramin

    Catalytically active colloids maintain non-equilibrium conditions in which they produce and deplete chemicals at their surface. While individual colloids that are symmetrically coated do not exhibit dynamical activity, the concentration fields resulting from their chemical activity decay as 1/r and produce gradients that attract or repel other colloids depending on their surface chemistry and ambient variables. This results in a non-equilibrium analogue of ionic systems, but with the remarkable novel feature of action-reaction symmetry breaking. In dilute conditions these active colloids join up to form molecules via generalized ionic bonds. Colloids are found to join up to form self-assembled molecules that could be inert or have spontaneous activity in the form of net translational velocity and spin depending on their symmetry properties and their constituents. As the interactions do not satisfy detailed-balance, it is possible to achieve structures with time dependent functionality. We study a molecule that adopts spontaneous oscillations and another that exhibits a run-and-tumble dynamics similar to bacteria. Our study shows that catalytically active colloids could be used for designing self-assembled structures that posses dynamical functionalities.

  18. Colloid-Facilitated Transport of Radionuclides through the Vadose Zone

    SciTech Connect

    Flury, Markus; Harsh, James B.; Zachara, John M.; Jin, Yan

    2002-06-01

    This project seeks to improve the basic understanding of colloid and colloid-facilitated transport of Cs in the vadose zone. The specific objectives are: (1) Determine the structure, composition, and surface charge characteristics of colloidal particles formed under conditions similar to those occurring during leakage of waste typical of Hanford tank supernatants into soils and sediments surrounding the tanks. (2) Characterize the mutual interactions between colloids, contaminant, and soil matrix in batch experiments under various ionic strength and pH conditions. We will investigate the nature of the solid-liquid interactions and the kinetics of the reactions. (3) Evaluate mobility of colloids through soil under different degrees of water saturation and solution chemistry (ionic strength and pH). (4) Determine the potential of colloids to act as carriers to transport the contaminant through the vadose zone and verify the results through comparison with field samples collected under leaking tanks. Results of this project will help to understand the fundamental mechanisms of Cs transport under the leaking Hanford tanks, and thus contribute to the long-term clean-up strategies at the Hanford site.

  19. Viscosity of colloidal suspensions

    SciTech Connect

    Cohen, E.G.D.; Schepper, I.M. de

    1995-12-31

    Simple expressions are given for the effective Newtonian viscosity as a function of concentration as well as for the effective visco-elastic response as a function of concentration and imposed frequency, of monodisperse neutral colloidal suspensions over the entire fluid range. The basic physical mechanisms underlying these formulae are discussed. The agreement with existing experiments is very good.

  20. Probing Interfacial Water on Nanodiamonds in Colloidal Dispersion.

    PubMed

    Petit, Tristan; Yuzawa, Hayato; Nagasaka, Masanari; Yamanoi, Ryoko; Osawa, Eiji; Kosugi, Nobuhiro; Aziz, Emad F

    2015-08-01

    The structure of interfacial water layers around nanoparticles dispersed in an aqueous environment may have a significant impact on their reactivity and on their interaction with biological species. Using transmission soft X-ray absorption spectroscopy in liquid, we demonstrate that the unoccupied electronic states of oxygen atoms from water molecules in aqueous colloidal dispersions of nanodiamonds have a different signature than bulk water. X-ray absorption spectroscopy can thus probe interfacial water molecules in colloidal dispersions. The impacts of nanodiamond surface chemistry and concentration on interfacial water electronic signature are discussed. PMID:26267179

  1. Light-activated self-propelled colloids

    PubMed Central

    Palacci, J.; Sacanna, S.; Kim, S.-H.; Yi, G.-R.; Pine, D. J.; Chaikin, P. M.

    2014-01-01

    Light-activated self-propelled colloids are synthesized and their active motion is studied using optical microscopy. We propose a versatile route using different photoactive materials, and demonstrate a multiwavelength activation and propulsion. Thanks to the photoelectrochemical properties of two semiconductor materials (α-Fe2O3 and TiO2), a light with an energy higher than the bandgap triggers the reaction of decomposition of hydrogen peroxide and produces a chemical cloud around the particle. It induces a phoretic attraction with neighbouring colloids as well as an osmotic self-propulsion of the particle on the substrate. We use these mechanisms to form colloidal cargos as well as self-propelled particles where the light-activated component is embedded into a dielectric sphere. The particles are self-propelled along a direction otherwise randomized by thermal fluctuations, and exhibit a persistent random walk. For sufficient surface density, the particles spontaneously form ‘living crystals’ which are mobile, break apart and reform. Steering the particle with an external magnetic field, we show that the formation of the dense phase results from the collisions heads-on of the particles. This effect is intrinsically non-equilibrium and a novel principle of organization for systems without detailed balance. Engineering families of particles self-propelled by different wavelength demonstrate a good understanding of both the physics and the chemistry behind the system and points to a general route for designing new families of self-propelled particles. PMID:25332383

  2. Generation of colloidal granules and capsules from double emulsion drops

    NASA Astrophysics Data System (ADS)

    Hess, Kathryn S.

    Assemblies of colloidal particles are extensively used in ceramic processing, pharmaceuticals, inks and coatings. In this project, the aim was to develop a new technique to fabricate monodispersed colloidal assemblies. The use of microfluidic devices and emulsion processing allows for the fabrication of complex materials that can be used in a variety of applications. A microfluidic device is used to create monodispersed water/oil/water (w/o/w) double emulsions with interior droplets of colloidal silica suspension ranging in size from tens to hundreds of microns. By tailoring the osmotic pressure using glycerol as a solute in the continuous and inner phases of the emulsion, we can control the final volume size of the monodispersed silica colloidal crystals that form in the inner droplets of the double emulsion. Modifying the ionic strength in the colloidal dispersion can be used to affect the particle-particle interactions and crystal formation of the final colloidal particle. This w/o/w technique has been used with other systems of metal oxide colloids and cellulose nanocrystals. Encapsulation of the colloidal suspension in a polymer shell for the generation of ceramic-polymer core-shell particles has also been developed. These core-shell particles have spawned new research in the field of locally resonant acoustic metamaterials. Systems and chemistries for creating cellulose hydrogels within the double emulsions have also been researched. Water in oil single emulsions and double emulsions have been used to create cellulose hydrogel spheres in the sub-100 micron diameter range. Oil/water/oil double emulsions allow us to create stable cellulose capsules. The addition of a second hydrogel polymer, such as acrylate or alginate, further strengthens the cellulose gel network and can also be processed into capsules and particles using the microfluidic device. This work could have promising applications in acoustic metamaterials, personal care products, pharmaceuticals

  3. COLLOIDS. Colloidal matter: Packing, geometry, and entropy.

    PubMed

    Manoharan, Vinothan N

    2015-08-28

    Colloidal particles with well-controlled shapes and interactions are an ideal experimental system for exploring how matter organizes itself. Like atoms and molecules, these particles form bulk phases such as liquids and crystals. But they are more than just crude analogs of atoms; they are a form of matter in their own right, with complex and interesting collective behavior not seen at the atomic scale. Their behavior is affected by geometrical or topological constraints, such as curved surfaces or the shapes of the particles. Because the interactions between the particles are often short-ranged, we can understand the effects of these constraints using geometrical concepts such as packing. The geometrical viewpoint gives us a window into how entropy affects not only the structure of matter, but also the dynamics of how it forms. PMID:26315444

  4. Colloidal Double Quantum Dots

    PubMed Central

    2016-01-01

    Conspectus Pairs of coupled quantum dots with controlled coupling between the two potential wells serve as an extremely rich system, exhibiting a plethora of optical phenomena that do not exist in each of the isolated constituent dots. Over the past decade, coupled quantum systems have been under extensive study in the context of epitaxially grown quantum dots (QDs), but only a handful of examples have been reported with colloidal QDs. This is mostly due to the difficulties in controllably growing nanoparticles that encapsulate within them two dots separated by an energetic barrier via colloidal synthesis methods. Recent advances in colloidal synthesis methods have enabled the first clear demonstrations of colloidal double quantum dots and allowed for the first exploratory studies into their optical properties. Nevertheless, colloidal double QDs can offer an extended level of structural manipulation that allows not only for a broader range of materials to be used as compared with epitaxially grown counterparts but also for more complex control over the coupling mechanisms and coupling strength between two spatially separated quantum dots. The photophysics of these nanostructures is governed by the balance between two coupling mechanisms. The first is via dipole–dipole interactions between the two constituent components, leading to energy transfer between them. The second is associated with overlap of excited carrier wave functions, leading to charge transfer and multicarrier interactions between the two components. The magnitude of the coupling between the two subcomponents is determined by the detailed potential landscape within the nanocrystals (NCs). One of the hallmarks of double QDs is the observation of dual-color emission from a single nanoparticle, which allows for detailed spectroscopy of their properties down to the single particle level. Furthermore, rational design of the two coupled subsystems enables one to tune the emission statistics from single

  5. Colloidal Double Quantum Dots.

    PubMed

    Teitelboim, Ayelet; Meir, Noga; Kazes, Miri; Oron, Dan

    2016-05-17

    Pairs of coupled quantum dots with controlled coupling between the two potential wells serve as an extremely rich system, exhibiting a plethora of optical phenomena that do not exist in each of the isolated constituent dots. Over the past decade, coupled quantum systems have been under extensive study in the context of epitaxially grown quantum dots (QDs), but only a handful of examples have been reported with colloidal QDs. This is mostly due to the difficulties in controllably growing nanoparticles that encapsulate within them two dots separated by an energetic barrier via colloidal synthesis methods. Recent advances in colloidal synthesis methods have enabled the first clear demonstrations of colloidal double quantum dots and allowed for the first exploratory studies into their optical properties. Nevertheless, colloidal double QDs can offer an extended level of structural manipulation that allows not only for a broader range of materials to be used as compared with epitaxially grown counterparts but also for more complex control over the coupling mechanisms and coupling strength between two spatially separated quantum dots. The photophysics of these nanostructures is governed by the balance between two coupling mechanisms. The first is via dipole-dipole interactions between the two constituent components, leading to energy transfer between them. The second is associated with overlap of excited carrier wave functions, leading to charge transfer and multicarrier interactions between the two components. The magnitude of the coupling between the two subcomponents is determined by the detailed potential landscape within the nanocrystals (NCs). One of the hallmarks of double QDs is the observation of dual-color emission from a single nanoparticle, which allows for detailed spectroscopy of their properties down to the single particle level. Furthermore, rational design of the two coupled subsystems enables one to tune the emission statistics from single photon

  6. Decreased Salinity and Actinide Mobility: Colloid-Facilitated Transport or pH Change?

    PubMed

    Haliena, Brian; Zheng, Hangping; Melson, Nathan; Kaplan, Daniel I; Barnett, Mark O

    2016-01-19

    Colloids have been implicated in influencing the transport of actinides and other adsorbed contaminants in the subsurface, significantly increasing their mobility. Such colloid-facilitated transport can be induced by changes in groundwater chemistry that occur, for example, when high ionic strength contaminant plumes are displaced by infiltrating rainwater. We studied the transport and mobility of Th(IV), as an analogue for Pu(IV) and other tetravalent actinides [An(IV)], in saturated columns packed with a natural heterogeneous subsurface sandy sediment. As expected, decreases in ionic strength both promoted the mobilization of natural colloids and enhanced the transport of previously adsorbed Th(IV). However, colloid-facilitated transport played only a minor role in enhancing the transport of Th(IV). Instead, the enhanced transport of Th(IV) was primarily due to the pH-dependent desorption of Th(IV) caused by the change in ionic strength. In contrast, the adsorption of Th(IV) had a marked impact on the surface charge of the sandy sediment, significantly affecting the mobility of the colloids. In the absence of Th(IV), changes in ionic strength were ineffective at releasing colloids while in the presence of Th(IV), decreases in ionic strength liberated significant concentrations of colloids. Therefore, under the conditions of our experiments which mimicked acidic, high ionic strength groundwater contaminant plumes, Th(IV) had a much greater effect on colloid transport than colloids had on Th(IV) transport. PMID:26687028

  7. Colloid migration in fractured media

    SciTech Connect

    Hunt, J.R. . Dept. of Civil Engineering)

    1989-09-15

    Field studies at the Nevada Test Site by researchers at Lawrence Livermore National Laboratory have demonstrated that radionuclides are being transported by colloidal material suspended in groundwater. This observation is counter to most predictions from contaminant transport models because the models assume adsorbed species are immobile. The purpose of this research is to quantify the transport processes for colloidal materials and develop the mechanistic understanding necessary to predict radionuclide transport in fractured media. There were three areas of investigation during this year that have addressed these issues: chemical control of colloid deposition on clean mineral surfaces, colloid accumulation on fracture surfaces, and the influence of deposited colloids on colloid and tracer migration. 7 refs.

  8. COLLOID-FACILITATED TRANSPORT OF RADIONUCLIDES THROUGH THE VADOSE ZONE

    SciTech Connect

    Flury, Markus

    2003-09-14

    Contaminants have leaked into the vadose zone at the USDOE Hanford reservation. It is important to understand the fate and transport of these contaminants to design remediation strategies and long-term waste management plans at the Hanford reservation. Colloids may play an important role in fate and transport of strongly sorbing contaminants, such as Cs or Pu. This project seeks to improve the basic understanding of colloid and colloid-facilitated transport of contaminants in the vadose zone. The specific objectives addressed are: (1) Determine the structure, composition, and surface charge characteristics of colloidal particles formed under conditions similar to those occurring during leakage of waste typical of Hanford tank supernatants into soils and sediments surrounding the tanks. (2) Characterize the mutual interactions between colloids, contaminant, and soil matrix in batch experiments under various ionic strength and pH conditions. We will investigate the nature of the solid-liquid interactions and the kinetics of the reactions. (3) Evaluate mobility of colloids through soil under different degrees of water saturation and solution chemistry (ionic strength and pH). (4) Determine the potential of colloids to act as carriers to transport the contaminant through the vadose zone and verify the results through comparison with field samples collected under leaking tanks. (5) Improve conceptual characterization of colloid-contaminant-soil interactions and colloid-facilitated transport for implementation into reactive chemical transport models. This project was in part supported by an NSF-IGERT grant to Washington State University. The IGERT grant provided funding for graduate student research and education, and two graduate students were involved in the EMSP project. The IGERT program also supported undergraduate internships. The project is part of a larger EMSP program to study fate and transport of contaminants under leaking Hanford waste tanks. The project has

  9. Mobile colloid generation induced by a cementitious plume: mineral surface-charge controls on mobilization.

    PubMed

    Li, Dien; Kaplan, Daniel I; Roberts, Kimberly A; Seaman, John C

    2012-03-01

    Cementitious materials are increasingly used as engineered barriers and waste forms for radiological waste disposal. Yet their potential effect on mobile colloid generation is not well-known, especially as it may influence colloid-facilitated contaminant transport. Whereas previous papers have studied the introduction of cement colloids into sediments, this study examined the influence of cement leachate chemistry on the mobilization of colloids from a subsurface sediment collected from the Savannah River Site, USA. A sharp mobile colloid plume formed with the introduction of a cement leachate simulant. Colloid concentrations decreased to background concentrations even though the aqueous chemical conditions (pH and ionic strength) remained unchanged. Mobile colloids were mainly goethite and to a lesser extent kaolinite. The released colloids had negative surface charges and the mean particle sizes ranged primarily from 200 to 470 nm. Inherent mineralogical electrostatic forces appeared to be the controlling colloid removal mechanism in this system. In the background pH of ~6.0, goethite had a positive surface charge, whereas quartz (the dominant mineral in the immobile sediment) and kaolinite had negative surface charges. Goethite acted as a cementing agent, holding kaolinite and itself onto the quartz surfaces due to the electrostatic attraction. Once the pH of the system was elevated, as in the cementitious high pH plume front, the goethite reversed to a negative charge, along with quartz and kaolinite, then goethite and kaolinite colloids were mobilized and a sharp spike in turbidity was observed. Simulating conditions away from the cementitious source, essentially no colloids were mobilized at 1:1000 dilution of the cement leachate or when the leachate pH was ≤ 8. Extreme alkaline pH environments of cementitious leachate may change mineral surface charges, temporarily promoting the formation of mobile colloids. PMID:22316126

  10. Graphical Synthesis of Colloid Transport Results on Quirk-Schofield Diagrams

    NASA Astrophysics Data System (ADS)

    Mays, D. C.

    2008-05-01

    The degree of colloid dispersion, or conversely the degree of flocculation, is crucial for understanding colloid transport in natural porous media, since it determines whether colloids are mobile or immobile. Additionally, in porous media containing more than a few percent fines, the degree of colloid dispersion also influences the permeability, and consequently the practicality of fluid extraction or injection. Colloid dispersion is largely determined by the aqueous chemistry, specifically pH, ionic strength, and sodium adsorption ratio (SAR). In the soil science literature, the effects of these three variables on colloid dispersion are commonly illustrated on Quirk-Schofield diagrams. In contrast, Quirk-Schofield diagrams appear to have been overlooked in the contaminant hydrology literature. This presentation will demonstrate the usefulness of Quirk-Schofield diagrams for presenting and interpreting a diversity of published colloid transport results, ranging from microbial pathogens to engineered nanoparticles to colloid-facilitated transport of metals. In particular, a quantitative analysis of published findings is presented using new Quirk-Schofield diagrams for kaolinite, illite, and montmorillonite, three clay minerals that are common in natural porous media. Additionally, because there is a relationship between colloid dispersion and permeability, this presentation will also show how Quirk-Schofield diagrams can provide insight into permeability changes, with applications to aquifer hydraulics and reservoir damage. The common aspects of all these results will be apparent, demonstrating that Quirk-Schofield diagrams are a simple, graphical technique that can be used to synthesize findings across the diverse applications where colloids play a central role. This study also suggests a framework for consistent reporting of colloid transport results: (1) measure the effects of pH, ionic strength, and SAR on colloid dispersion; (2) report results on Quirk

  11. Doping for speed: colloidal nanoparticles for thin-film optoelectronics.

    PubMed

    Noone, Kevin M; Ginger, David S

    2009-02-24

    Solution-processable semiconductor materials ranging from conjugated polymers and small organic molecules to colloidal inorganic nanoparticles are being studied for applications in both low-cost solar cells and photodetectors. High-quality thin films of many inorganic semiconductors can be prepared by techniques such as chemical vapor deposition, molecular beam epitaxy, and atomic layer deposition. In contrast, preparing device-quality films of inorganic materials from colloidal solutions can be more difficult due to the challenge of achieving well-defined doping, controlled trap densities, and reproducible surface chemistry. Nevertheless, solution deposition using colloidal precursors is an attractive goal because of the potential for low-cost, large-area processing. In recent years, a great deal of effort has focused on the colloidal synthesis of wide-band-gap metal oxides such as TiO(2), visible-absorbing II-VI compounds such as CdSe, and small-band-gap materials such as PbSe. Much of the work on visible- and IR-absorbing photodetectors has been done on materials containing metals such as Cd and Pb. A new paper in this issue demonstrates photoconductive detectors made from Cu-containing In(2)S(3) nanoplates. The incorporation of Cu into the In(2)S(3) nanoplates leads to a significant decrease in the lifetime of the photoexcited carriers, resulting in significantly faster response times for the photodetectors processed from colloidal solution. PMID:19236059

  12. Self-assembly of active colloidal molecules with dynamic function

    NASA Astrophysics Data System (ADS)

    Soto, Rodrigo; Golestanian, Ramin

    2015-05-01

    Catalytically active colloids maintain nonequilibrium conditions in which they produce and deplete chemicals and hence effectively act as sources and sinks of molecules. While individual colloids that are symmetrically coated do not exhibit any form of dynamical activity, the concentration fields resulting from their chemical activity decay as 1 /r and produce gradients that attract or repel other colloids depending on their surface chemistry and ambient variables. This results in a nonequilibrium analog of ionic systems, but with the remarkable novel feature of action-reaction symmetry breaking. We study solutions of such chemically active colloids in dilute conditions when they join up to form molecules via generalized ionic bonds and discuss how we can achieve structures with time-dependent functionality. In particular, we study a molecule that adopts a spontaneous oscillatory pattern of conformations and another that exhibits a run-and-tumble dynamics similar to bacteria. Our study shows that catalytically active colloids could be used for designing self-assembled structures that possess dynamical functionalities that are determined by their prescribed three-dimensional structures, a strategy that follows the design principle of proteins.

  13. Organized thiol functional groups in mesoporous core shell colloids

    SciTech Connect

    Marchena, Martin H.; Granada, Mara; Bordoni, Andrea V.; Joselevich, Maria; Troiani, Horacio; Williams, Federico J.; Wolosiuk, Alejandro

    2012-03-15

    The co-condensation in situ of tetraethoxysilane (TEOS) and mercaptopropyltrimethoxysilane (MPTMS) using cetyltrimethylammonium bromide (CTAB) as a template results in the synthesis of multilayered mesoporous structured SiO{sub 2} colloids with 'onion-like' chemical environments. Thiol groups were anchored to an inner selected SiO{sub 2} porous layer in a bilayered core shell particle producing different chemical regions inside the colloidal layered structure. X-Ray Photoelectron Spectroscopy (XPS) shows a preferential anchoring of the -SH groups in the double layer shell system, while porosimetry and simple chemical modifications confirm that pores are accessible. We can envision the synthesis of interesting colloidal objects with defined chemical environments with highly controlled properties. - Graphical abstract: Mesoporous core shell SiO{sub 2} colloids with organized thiol groups. Highlights: Black-Right-Pointing-Pointer Double shell mesoporous silica colloids templated with CTAB. Black-Right-Pointing-Pointer Sequential deposition of mesoporous SiO{sub 2} layers with different chemistries. Black-Right-Pointing-Pointer XPS shows the selective functionalization of mesoporous layers with thiol groups.

  14. Magnetofluidic Tweezing of Nonmagnetic Colloids.

    PubMed

    Timonen, Jaakko V I; Demirörs, Ahmet F; Grzybowski, Bartosz A

    2016-05-01

    Magnetofluidic tweezing based on negative magnetophoresis and microfabricated core-shell magnetic microtips allows controlled on-demand assembly of colloids and microparticles into various static and dynamic structures such as colloidal crystals (as shown for 3.2 μm silica particles). PMID:26990182

  15. Effect of hydrofracking fluid on colloid transport in the unsaturated zone.

    PubMed

    Sang, Wenjing; Stoof, Cathelijne R; Zhang, Wei; Morales, Verónica L; Gao, Bin; Kay, Robert W; Liu, Lin; Zhang, Yalei; Steenhuis, Tammo S

    2014-07-15

    Hydraulic fracturing is expanding rapidly in the US to meet increasing energy demand and requires high volumes of hydrofracking fluid to displace natural gas from shale. Accidental spills and deliberate land application of hydrofracking fluids, which return to the surface during hydrofracking, are common causes of environmental contamination. Since the chemistry of hydrofracking fluids favors transport of colloids and mineral particles through rock cracks, it may also facilitate transport of in situ colloids and associated pollutants in unsaturated soils. We investigated this by subsequently injecting deionized water and flowback fluid at increasing flow rates into unsaturated sand columns containing colloids. Colloid retention and mobilization was measured in the column effluent and visualized in situ with bright field microscopy. While <5% of initial colloids were released by flushing with deionized water, 32-36% were released by flushing with flowback fluid in two distinct breakthrough peaks. These peaks resulted from 1) surface tension reduction and steric repulsion and 2) slow kinetic disaggregation of colloid flocs. Increasing the flow rate of the flowback fluid mobilized an additional 36% of colloids, due to the expansion of water filled pore space. This study suggests that hydrofracking fluid may also indirectly contaminate groundwater by remobilizing existing colloidal pollutants. PMID:24905470

  16. Impact of Dissolved Organic Matter on Colloid Transport in the Vadose Zone

    NASA Astrophysics Data System (ADS)

    Morales, V. L.; Gao, B.; Steenhuis, T. S.

    2008-05-01

    Mobile soil colloids can facilitate contaminant transport through the soil profile through complexation of pollutants previously thought to have very limited mobility in soil. Much work has been done to define the governing transport mechanisms of colloids in unsaturated media, and have demonstrated that the release, transport, and retention of colloidal particles in soil are very sensitive to flow chemistry. However, better understanding of the physicochemical interactions between dissolved organic matter (DOM) and soil colloids is clearly needed, as the transport in manure rich soils has been observed to be much greater than originally suspected. The goal of this study is to fill this knowledge gap by elucidating the role of DOM on the transport and retention of colloidal particles in the vadose zone through multi-scale investigations. The initial phase of the experimental work consists of collecting concomitant visual (with Bright Field Microscopy and Confocal Laser Scanning Microscopy) and breakthrough data from medium sized (d50 = 0.4 mm) quartz sand filled chambers of 10x2x2 cm and 1 cm diameter x 10 cm length. Pulses of synthetic and clay colloid suspensions will be individually injected into the flow chambers at various concentrations of DOM (i.e. extracted humic acid from manure). Results from these experiments indicate that DOM can increase colloid stability in water and thereby potentially facilitate the transport of contaminants adsorbed onto suspended and mobile colloids.

  17. Effect of Hydrofracking Fluid on Colloid Transport in the Unsaturated Zone

    PubMed Central

    2014-01-01

    Hydraulic fracturing is expanding rapidly in the US to meet increasing energy demand and requires high volumes of hydrofracking fluid to displace natural gas from shale. Accidental spills and deliberate land application of hydrofracking fluids, which return to the surface during hydrofracking, are common causes of environmental contamination. Since the chemistry of hydrofracking fluids favors transport of colloids and mineral particles through rock cracks, it may also facilitate transport of in situ colloids and associated pollutants in unsaturated soils. We investigated this by subsequently injecting deionized water and flowback fluid at increasing flow rates into unsaturated sand columns containing colloids. Colloid retention and mobilization was measured in the column effluent and visualized in situ with bright field microscopy. While <5% of initial colloids were released by flushing with deionized water, 32–36% were released by flushing with flowback fluid in two distinct breakthrough peaks. These peaks resulted from 1) surface tension reduction and steric repulsion and 2) slow kinetic disaggregation of colloid flocs. Increasing the flow rate of the flowback fluid mobilized an additional 36% of colloids, due to the expansion of water filled pore space. This study suggests that hydrofracking fluid may also indirectly contaminate groundwater by remobilizing existing colloidal pollutants. PMID:24905470

  18. Colloidal analogs of molecular chain stoppers

    PubMed Central

    Klinkova, Anna; Thérien-Aubin, Héloïse; Choueiri, Rachelle M.; Rubinstein, Michael; Kumacheva, Eugenia

    2013-01-01

    A similarity between chemical reactions and self-assembly of nanoparticles offers a strategy that can enrich both the synthetic chemistry and the nanoscience fields. Synthetic methods should enable quantitative control of the structural characteristics of nanoparticle ensembles such as their aggregation number or directionality, whereas the capability to visualize and analyze emerging nanostructures using characterization tools can provide insight into intelligent molecular design and mechanisms of chemical reactions. We explored this twofold concept for an exemplary system including the polymerization of bifunctional nanoparticles in the presence of monofunctional colloidal chain stoppers. Using reaction-specific design rules, we synthesized chain stoppers with controlled reactivity and achieved quantitative fine-tuning of the self-assembled structures. Analysis of the nanostructures provided information about polymerization kinetics, side reactions, and the distribution of all of the species in the reaction system. A quantitative model was developed to account for the reactivity, kinetics, and side reactions of nanoparticles, all governed by the design of colloidal chain stoppers. This work provided the ability to test theoretical models developed for molecular polymerization. PMID:24190993

  19. Silver clusters and chemistry in zeolites

    SciTech Connect

    Sun, T.; Seff, K. . Dept. of Chemistry)

    1994-06-01

    The spectroscopic work done on silver clusters trapped in solid noble gas matrices at low temperature has been extensively reviewed by Ozin, and Henglein has done the same for photochemical studies of colloidal silver particles in solution. This article will review the chemistry of silver in zeolite hosts, including the synthesis and structures of silver clusters. 127 refs.

  20. MOLECULAR DESIGN OF COLLOIDS IN SUPERCRITICAL FLUIDS

    SciTech Connect

    Keith P. Johnston

    2009-04-06

    The environmentally benign, non-toxic, non-flammable fluids water and carbon dioxide (CO2) are the two most abundant and inexpensive solvents on earth. Emulsions of these fluids are of interest in many industrial processes, as well as CO2 sequestration and enhanced oil recovery. Until recently, formation of these emulsions required stabilization with fluorinated surfactants, which are expensive and often not environmentally friendly. In this work we overcame this severe limitation by developing a fundamental understanding of the properties of surfactants the CO2-water interface and using this knowledge to design and characterize emulsions stabilized with either hydrocarbon-based surfactants or nanoparticle stabilizers. We also discovered a new concept of electrostatic stabilization for CO2-based emulsions and colloids. Finally, we were able to translate our earlier work on the synthesis of silicon and germanium nanocrystals and nanowires from high temperatures and pressures to lower temperatures and ambient pressure to make the chemistry much more accessible.

  1. Colloidal aggregation in polymer blends.

    PubMed

    Benhamou, M; Ridouane, H; Hachem, E-K; Derouiche, A; Rahmoune, M

    2005-06-22

    We consider here a low-density assembly of colloidal particles immersed in a critical polymer mixture of two chemically incompatible polymers. We assume that, close to the critical point of the free mixture, the colloids prefer to be surrounded by one polymer (critical adsorption). As result, one is assisted to a reversible colloidal aggregation in the nonpreferred phase, due the existence of a long-range attractive Casimir force between particles. This aggregation is a phase transition driving the colloidal system from dilute to dense phases, as the usual gas-liquid transition. We are interested in a quantitative investigation of the phase diagram of the immersed colloids. We suppose that the positions of particles are disordered, and the disorder is quenched and follows a Gaussian distribution. To apprehend the problem, use is made of the standard phi(4) theory, where the field phi represents the composition fluctuation (order parameter), combined with the standard cumulant method. First, we derive the expression of the effective free energy of colloids and show that this is of Flory-Huggins type. Second, we find that the interaction parameter u between colloids is simply a linear combination of the isotherm compressibility and specific heat of the free mixture. Third, with the help of the derived effective free energy, we determine the complete shape of the phase diagram (binodal and spinodal) in the (Psi,u) plane, with Psi as the volume fraction of immersed colloids. The continuous "gas-liquid" transition occurs at some critical point K of coordinates (Psi(c) = 0.5,u(c) = 2). Finally, we emphasize that the present work is a natural extension of that, relative to simple liquid mixtures incorporating colloids. PMID:16035822

  2. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1972

    1972-01-01

    Short articles describe techniques for demonstrating corrosion of metallic couples, colloidal dispersion of light, the biodegradability of detergents, the laboratory preparation of chlorine in model electrolytic cells, and the detection of food colorings in candy. (AL)

  3. Colloids in Acute Burn Resuscitation.

    PubMed

    Cartotto, Robert; Greenhalgh, David

    2016-10-01

    Colloids have been used in varying capacities throughout the history of formula-based burn resuscitation. There is sound experimental evidence that demonstrates colloids' ability to improve intravascular colloid osmotic pressure, expand intravascular volume, reduce resuscitation requirements, and limit edema in unburned tissue following a major burn. Fresh frozen plasma appears to be a useful and effective immediate burn resuscitation fluid but its benefits must be weighed against its costs, and risks of viral transmission and acute lung injury. Albumin, in contrast, is less expensive and safer and has demonstrated ability to reduce resuscitation requirements and possibly limit edema-related morbidity. PMID:27600123

  4. Two-dimensional dipolar nematic colloidal crystals.

    PubMed

    Skarabot, M; Ravnik, M; Zumer, S; Tkalec, U; Poberaj, I; Babic, D; Osterman, N; Musevic, I

    2007-11-01

    We study the interactions and directed assembly of dipolar nematic colloidal particles in planar nematic cells using laser tweezers. The binding energies for two stable configurations of a colloidal pair with homeotropic surface alignment are determined. It is shown that the orientation of the dipolar colloidal particle can efficiently be controlled and changed by locally quenching the nematic liquid crystal from the laser-induced isotropic phase. The interaction of a single colloidal particle with a single colloidal chain is determined and the interactions between pairs of colloidal chains are studied. We demonstrate that dipolar colloidal chains self-assemble into the two-dimensional (2D) dipolar nematic colloidal crystals. An odd-even effect is observed with increasing number of colloidal chains forming the 2D colloidal crystal. PMID:18233658

  5. Colloid labelled with radionuclide and method

    DOEpatents

    Atcher, Robert W.; Hines, John J.

    1990-01-01

    A ferric hydroxide colloid having an alpha-emitting radionuclide essentially on the outer surfaces and a method of forming same. The method includes oxidizing a ferrous hydroxide to ferric hydroxide in the presence of a preselected radionuclide to form a colloid having the radionuclide on the outer surface thereof, and thereafter washing the colloid, and suspending the washed colloid in a suitable solution. The labelled colloid is useful in cancer therapy and for the treatment of inflamed joints.

  6. Method of making colloid labeled with radionuclide

    DOEpatents

    Atcher, Robert W.; Hines, John J.

    1991-01-01

    A ferric hydroxide colloid having an alpha-emitting radionuclide essentially on the outer surfaces and a method of forming same. The method includes oxidizing a ferrous hydroxide to ferric hydroxide in the presence of a preselected radionuclide to form a colloid having the radionuclide on the outer surface thereof, and thereafter washing the colloid, and suspending the washed colloid in a suitable solution. The labelled colloid is useful in cancer therapy and for the treatment of inflamed joints.

  7. Colloid labelled with radionuclide and method

    DOEpatents

    Atcher, R.W.; Hines, J.J.

    1990-11-13

    A ferric hydroxide colloid having an alpha-emitting radionuclide essentially on the outer surfaces and a method of forming same. The method includes oxidizing a ferrous hydroxide to ferric hydroxide in the presence of a preselected radionuclide to form a colloid having the radionuclide on the outer surface thereof, and thereafter washing the colloid, and suspending the washed colloid in a suitable solution. The labelled colloid is useful in cancer therapy and for the treatment of inflamed joints. No Drawings

  8. Quantification of Capillary Force Acting on Colloids in a Three-phase Model System of Partially Saturated Porous Media

    NASA Astrophysics Data System (ADS)

    Zhang, W.; Morales, V. L.; Gao, B.; Geohring, L. D.; Parlange, J.; Hay, A. G.; Steenhuis, T. S.

    2008-12-01

    Colloid transport in the vadose zone has gained increasing importance due to groundwater contamination of colloidal-size pathogens and colloid-facilitated transport of contaminants. Although colloid transport in saturated system is well understood, the presence of air phase in partially saturated zone poses an additional challenge for elucidating the mechanisms of the colloid transport. Capillary forces that occur when a colloid protrudes through water film around the grain or near air-water meniscus-solid interface has been identified as the major mechanism for colloid retention. Capillary force could be several orders of magnitude greater than the electrostatic DLVO force. Our current study investigates the effect of colloid surface properties, fluid chemistry, and film thickness on capillary force and associated meniscus configuration in a three-phase model system consisting of a particle protruding out of a spread film. Particles ranging from 100 to 600 micrometer are used as surrogates for colloids since the menisci of colloids cannot be visualized using currently available microscopic resolution. In our experimental setup, menisci configuration of soda-lime glass beads and polystyrene beads are visualized with high resolution Hirox digital bright field microscope in dionized water and solutions of 1:1 electrolyte (NaCl), 1:2 electrolyte (CaCl2), natural organic matters, and anionic, cationic or nonionic surfactants. The hydrophilic glass beads can be made hydrophobic by treating with octadecyltrichlorosilane, while the hydrophobic polystyrene can be made hydrophilic by carboxylation. The film thickness is also varied by allowing for evaporation. Contact angle, radius of three-phase contact line, and other relevant parameters for calculation of capillary force are measured. The changes of surface properties, fluid chemistry, and film thickness are expected to result in the observable changes of capillary force and associated meniscus configuration. This

  9. Engineering colloidal assembly via biological adhesion

    NASA Astrophysics Data System (ADS)

    Hiddessen, Amy Lynn

    Due to highly specialized recognition properties, biological receptor-ligand interactions offer valuable tools for engineering the assembly of novel colloidal materials. A unique sub-class of these macromolecules, called selectins, was exploited to develop binary suspensions where particles are programmed to associate reversibly or irreversibly via specific biomolecular cross-linking. Flow cytometry and videomicroscopy were used to examine factors controlling suspension assembly and structure, including biomolecular affinity and density, and individual and total particle volume fractions. By functionalizing small (RA = 0.47 mum) and larger (RB = 2.75 mum) particles with high surface densities of complementary E-selectin/sialyl Lewis X (sLeX) carbohydrate chemistry, a series of structures, from colloidal micelles (large particle coated with smaller particles) and clusters, to rings and elongated chains, was synthesized by decreasing the number ratio, NA/NB, of small (A) to large (B) particles (2 ≤ NA/NB ≤ 200) at low total volume fraction (10-4 ≤ φT ≤ 10-3 ). Using significantly lower surface densities, the low affinity binding between E-selectin and sLeX was exploited to create particles that interact reversibly, and average particle interaction lifetimes were tuned from minutes down to single selectin-carbohydrate bond lifetimes (≈1 s) by reducing sLeX density, a significant step toward assembling ordered microstructures. Particle binding lifetimes were analyzed with a receptor-ligand binding model, yielding estimates for molecular parameters, including on rate, 10-2 s-1 < kon < 10-1 s-1, and unstressed off rate, 0.25 s-1 ≤ kor ≤ 1.0 s-1, that characterize the docking dynamics of particles. Finally, at significantly higher volume fraction (φ T ≥ 10-1) and low number ratio, the rheology of space-filling networks crosslinked by high affinity streptavidin-biotin chemistry was probed to acquire knowledge on bulk properties of biocolloidal suspensions

  10. Emergent behavior in active colloids

    NASA Astrophysics Data System (ADS)

    Zöttl, Andreas; Stark, Holger

    2016-06-01

    Active colloids are microscopic particles, which self-propel through viscous fluids by converting energy extracted from their environment into directed motion. We first explain how artificial microswimmers move forward by generating near-surface flow fields via self-phoresis or the self-induced Marangoni effect. We then discuss generic features of the dynamics of single active colloids in bulk and in confinement, as well as in the presence of gravity, field gradients, and fluid flow. In the third section, we review the emergent collective behavior of active colloidal suspensions, focusing on their structural and dynamic properties. After summarizing experimental observations, we give an overview of the progress in modeling collectively moving active colloids. While active Brownian particles are heavily used to study collective dynamics on large scales, more advanced methods are necessary to explore the importance of hydrodynamic and phoretic particle interactions. Finally, the relevant physical approaches to quantify the emergent collective behavior are presented.

  11. Colloidal Suspended Iron in Rivers

    NASA Astrophysics Data System (ADS)

    Shiller, A. M.

    2009-12-01

    Iron is transported in most rivers predominantly in two physical-chemical forms: a) organic complexes of Fe(III) and b) crystalline or poorly-ordered suspended phases frequently dominated by iron oxides. These two forms have different properties with respect to transport, bioavailability, and sorption. For the suspended phase iron, the fraction in the colloidal size range may be especially important given the interactions of ferric oxide surfaces with dissolved metal ions and organic compounds. We report the concentrations of colloidal (20 - 450 nm) suspended particulate iron in a wide variety of rivers. Goals of this effort are to ascertain the ubiquity of this material and also to examine other fluvial variables as indicators of its sources and nature. This, in turn, should lead to an understanding of how landscape/climate change could affect fluvial colloidal suspended iron. Possible sources of suspended colloidal iron include ferric oxides precipitated from the oxidation of ferrous iron derived from reducing environments, alumino-silicates derived from physical weathering, products of chemical weathering, and flushing of soils. We observe most commonly that increasing concentrations of colloidal suspended iron follow indicators of reducing sources (e.g., higher dissolved Mn and Ce anomaly close to 1), suggesting that this material is dominated by freshly precipitated iron oxides. Only in glacial watersheds do we find colloidal suspended iron instead correlating with colloidal suspended Si, and hence, likely to be associated with alumino-silicates. We also observe that colloidal suspended iron correlates well with the UV absorbance associated with this size range (20 - 450 nm).

  12. Re-shaping colloidal clusters

    NASA Astrophysics Data System (ADS)

    Kraft, Daniela

    2015-03-01

    Controlling the geometry and yield of anisotropic colloidal particles remains a challenge for hierarchical self-assembly. I will discuss a synthetic strategy for fabricating colloidal clusters by creating order in randomly aggregated polymer spheres using surface tension and geometrical constraints. The technique can be extended to a variety of charge-stabilized polymer spheres and offers control over the cluster size distribution. VENI grant from The Netherlands Organization for Scientific Research (NWO).

  13. Aggregation of Heterogeneously Charged Colloids.

    PubMed

    Dempster, Joshua M; Olvera de la Cruz, Monica

    2016-06-28

    Patchy colloids are attractive as programmable building blocks for metamaterials. Inverse patchy colloids, in which a charged surface is decorated with patches of the opposite charge, are additionally noteworthy as models for heterogeneously charged biological materials such as proteins. We study the phases and aggregation behavior of a single charged patch in an oppositely charged colloid with a single-site model. This single-patch inverse patchy colloid model shows a large number of phases when varying patch size. For large patch sizes we find ferroelectric crystals, while small patch sizes produce cross-linked gels. Intermediate values produce monodisperse clusters and unusual worm structures that preserve finite ratios of area to volume. The polarization observed at large patch sizes is robust under extreme disorder in patch size and shape. We examine phase-temperature dependence and coexistence curves and find that large patch sizes produce polarized liquids, in contrast to mean-field predictions. Finally, we introduce small numbers of unpatched charged colloids. These can either suppress or encourage aggregation depending on their concentration and the size of the patches on the patched colloids. These effects can be exploited to control aggregation and to measure effective patch size. PMID:27253725

  14. Toward Coordinated Colloids: Site-Selective Growth of Titania on Patchy Silica Particles

    PubMed Central

    Bae, Changdeuck; Kim, Hyunchul; Montero Moreno, Josep M.; Yi, Gi-Ra; Shin, Hyunjung

    2015-01-01

    Rational synthesis of coordinated spherical colloids is reported by site-selective growth of secondary hemispherical patches on primary spherical particles with quasi-defined coordination numbers and positions. We clarify the importance of mass transport phenomena on the site-specific secondary nucleation/growth in nanoparticulate colloidal systems. By comparing ultrasonic and conventional agitation during patch growth, we found that enhanced mass transfer is the key to controlled, homogeneous transport of the molecular precursors in a solvent onto the nanoparticles. With chemically defined nucleation sites, the surfaces of spherical silica particles were modified for use as a new kind of colloid with patches at desired coordination positions. Our observations represent a significant breakthrough in colloidal chemistry and self-assembly. PMID:25797616

  15. Characteristics of aqueous colloids generated by corrosion of metallic uranium fuel.

    SciTech Connect

    Fortner, J. A.; Mertz, C. J.; Goldberg, M. M.; Siefert, S.

    2002-09-12

    Metallic uranium fuel from the Hanford N Reactor was corroded in aqueous solutions and the resulting colloidal suspensions were analyzed to determine particle size, morphology, population, and radionuclide association. The experiments used a range of solution chemistry conditions including deionized water, single salt solutions, and modified groundwater from Yucca Mountain. Colloids were analyzed by inductively coupled plasma mass spectrometry, transmission electron microscopy, photon correlation spectroscopy, and synchrotron small-angle x-ray scattering. The results of these analyses indicate that stable suspensions of small (1-10 nm diameter), spherical uranium oxides are generated and aggregate to approximately 100-200 nm colloids. There is no indication that these colloids continue to aggregate to larger size. In silicate solutions, large acicular uranium silicate colloids are formed in small quantities as are large uranium-bearing smectite clay colloids. Plutonium clearly associates with colloidal particles. Large particles contain the same Pu/U ratio as the uncorroded fuel, possibly indicating that the Pu is incorporated in the particle matrix. Smaller particles are highly enriched in Pu relative to the uncorroded fuel.

  16. Chemical Routes to Colloidal Chalcogenide Nanosheets

    SciTech Connect

    Schaak, Raymond

    2015-02-19

    This project sought to develop new low-temperature synthetic pathways to intermetallic and chalcogenide nanostructures and powders, with an emphasis on systems that are relevant to advancing the synthesis, processing, and discovery of superconducting materials. The primary synthetic routes involved solution chemistry methods, and several fundamental synthetic challenges that underpinned the formation of these materials were identified and investigated. Methods for incorporating early transition metals and post transition metals into nanoscale and bulk crystals using low-temperature solution chemistry methods were developed and studied, leading to colloidal nanocrystals of elemental indium, manganese, and germanium, as well as nanocrystalline and bulk intermetallic compounds containing germanium, gallium, tin, indium, zinc, bismuth, and lithium. New chemical tools were developed to help target desired phases in complex binary intermetallic and metal chalcogenide systems that contain multiple stable phases, including direct synthesis methods and chemical routes that permit post-synthetic modification. Several phases that are metastable in bulk systems were targeted, synthesized, and characterized as nanocrystalline solids and bulk powders, including the L12-type intermetallic compounds Au3Fe, Au3Ni, and Au3Co, as well as wurtzite-type MnSe. Methods for accessing crystalline metal borides and carbides using direct solution chemistry methods were also developed, with an emphasis on Ni3B and Ni3C, which revealed useful correlations of composition and magnetic properties. Methods for scale-up and nanoparticle purification were explored, providing access to centimeter-scale pressed pellets of polyol-synthesized nanopowders and a bacteriophage-mediated method for separating impure nanoparticle mixtures into their components. Several advances were made in the synthesis of iron selenide and related superconducting materials, including the production of colloidal Fe

  17. Dielectrophoresis force of colloidal nanoparticles

    NASA Astrophysics Data System (ADS)

    Huang, Hao; Ou-Yang, Daniel

    Dielectrophoresis (DEP) is the motion of a polarizable colloidal particle in a non­uniform electric field. The magnitude of the DEP force is known to be proportional to the gradient of E2. The DEP force also depends on the relative polarizability of the particle to that of the surrounding medium. Due to its ease of use, DEP has been proposed for a variety of applications to manipulate colloidal particles in a microfluidic setting. However, accurate measurements of the DEP force on colloidal nanoparticles are lacking. A new method is proposed to measure accurately the DEP potential force of colloidal nanoparticles by using confocal fluorescence imaging to determine the density distributions of dilute colloidal nanoparticle in a DEP potential force field. The DEP potential field can be calculated from the particle density distributions since the spatial distribution of the particle number density follows the Boltzmann distribution of the DEP potential energy. The validity of the measured DEP force is tested by examining the force as a function of the E field strength and particle size. The classic Maxwell­Wagner­O'Konski is found to be inadequate to fully describe the frequency dependence of the DEP force. NSF 0928299, Emulsion Polymer Institute, Department of Physics of Lehigh University.

  18. Laboratory investigation of the role of desorption kinetics on americium transport associated with bentonite colloids.

    PubMed

    Dittrich, Timothy Mark; Boukhalfa, Hakim; Ware, Stuart Douglas; Reimus, Paul William

    2015-10-01

    Understanding the parameters that control colloid-mediated transport of radionuclides is important for the safe disposal of used nuclear fuel. We report an experimental and reactive transport modeling examination of americium transport in a groundwater-bentonite-fracture fill material system. A series of batch sorption and column transport experiments were conducted to determine the role of desorption kinetics from bentonite colloids in the transport of americium through fracture materials. We used fracture fill material from a shear zone in altered granodiorite collected from the Grimsel Test Site (GTS) in Switzerland and colloidal suspensions generated from FEBEX bentonite, a potential repository backfill material. The colloidal suspension (100 mg L(-1)) was prepared in synthetic groundwater that matched the natural water chemistry at GTS and was spiked with 5.5 × 10(-10) M (241)Am. Batch characterizations indicated that 97% of the americium in the stock suspension was adsorbed to the colloids. Breakthrough experiments conducted by injecting the americium colloidal suspension through three identical columns in series, each with mean residence times of 6 h, show that more than 95% of the bentonite colloids were transported through each of the columns, with modeled colloid filtration rates (k(f)) of 0.01-0.02 h(-1). Am recoveries in each column were 55-60%, and Am desorption rate constants from the colloids, determined from 1-D transport modeling, were 0.96, 0.98, and 0.91 h(-1) in the three columns, respectively. The consistency in Am recoveries and desorption rate constants in each column indicates that the Am was not associated with binding sites of widely-varying strengths on the colloids, as one binding site with fast kinetics represented the system accurately for all three sequential columns. Our data suggest that colloid-mediated transport of Am in a bentonite-fracture fill material system is unlikely to result in transport over long distance scales because

  19. Laboratory investigation of the role of desorption kinetics on americium transport associated with bentonite colloids

    DOE PAGESBeta

    Dittrich, Timothy Mark; Boukhalfa, Hakim; Ware, Stuart Douglas; Reimus, Paul William

    2015-07-13

    Understanding the parameters that control colloid-mediated transport of radionuclides is important for the safe disposal of used nuclear fuel. We report an experimental and reactive transport modeling examination of americium transport in a groundwater–bentonite–fracture fill material system. A series of batch sorption and column transport experiments were conducted to determine the role of desorption kinetics from bentonite colloids in the transport of americium through fracture materials. We used fracture fill material from a shear zone in altered granodiorite collected from the Grimsel Test Site (GTS) in Switzerland and colloidal suspensions generated from FEBEX bentonite, a potential repository backfill material. Themore » colloidal suspension (100 mg L–1) was prepared in synthetic groundwater that matched the natural water chemistry at GTS and was spiked with 5.5 × 10–10 M241Am. Batch characterizations indicated that 97% of the americium in the stock suspension was adsorbed to the colloids. Breakthrough experiments conducted by injecting the americium colloidal suspension through three identical columns in series, each with mean residence times of 6 h, show that more than 95% of the bentonite colloids were transported through each of the columns, with modeled colloid filtration rates (kf) of 0.01–0.02 h–1. Am recoveries in each column were 55–60%, and Am desorption rate constants from the colloids, determined from 1-D transport modeling, were 0.96, 0.98, and 0.91 h–1 in the three columns, respectively. The consistency in Am recoveries and desorption rate constants in each column indicates that the Am was not associated with binding sites of widely-varying strengths on the colloids, as one binding site with fast kinetics represented the system accurately for all three sequential columns. As a result, our data suggest that colloid-mediated transport of Am in a bentonite-fracture fill material system is unlikely to result in transport over long

  20. Laboratory investigation of the role of desorption kinetics on americium transport associated with bentonite colloids

    SciTech Connect

    Dittrich, Timothy Mark; Boukhalfa, Hakim; Ware, Stuart Douglas; Reimus, Paul William

    2015-07-13

    Understanding the parameters that control colloid-mediated transport of radionuclides is important for the safe disposal of used nuclear fuel. We report an experimental and reactive transport modeling examination of americium transport in a groundwater–bentonite–fracture fill material system. A series of batch sorption and column transport experiments were conducted to determine the role of desorption kinetics from bentonite colloids in the transport of americium through fracture materials. We used fracture fill material from a shear zone in altered granodiorite collected from the Grimsel Test Site (GTS) in Switzerland and colloidal suspensions generated from FEBEX bentonite, a potential repository backfill material. The colloidal suspension (100 mg L–1) was prepared in synthetic groundwater that matched the natural water chemistry at GTS and was spiked with 5.5 × 10–10 M241Am. Batch characterizations indicated that 97% of the americium in the stock suspension was adsorbed to the colloids. Breakthrough experiments conducted by injecting the americium colloidal suspension through three identical columns in series, each with mean residence times of 6 h, show that more than 95% of the bentonite colloids were transported through each of the columns, with modeled colloid filtration rates (kf) of 0.01–0.02 h–1. Am recoveries in each column were 55–60%, and Am desorption rate constants from the colloids, determined from 1-D transport modeling, were 0.96, 0.98, and 0.91 h–1 in the three columns, respectively. The consistency in Am recoveries and desorption rate constants in each column indicates that the Am was not associated with binding sites of widely-varying strengths on the colloids, as one binding site with fast kinetics represented the system accurately for all three sequential columns. As a result, our data suggest that colloid-mediated transport of Am in a bentonite-fracture fill

  1. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1972

    1972-01-01

    Thirteen ideas are presented that may be of use to chemistry teachers. Topics covered include vitamin C, industrial chemistry, electrical conductivity, electrolysis, alkali metals, vibration modes infra-red, dynamic equilibrium, and some new demonstrations in gaseous combinations. (PS)

  2. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1976

    1976-01-01

    Described are eight chemistry experiments and demonstrations applicable to introductory chemistry courses. Activities include: measure of lattice enthalpy, Le Chatelier's principle, decarboxylation of soap, use of pocket calculators in pH measurement, and making nylon. (SL)

  3. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1983

    1983-01-01

    Presents background information, laboratory procedures, classroom materials/activities, and chemistry experiments. Topics include sublimation, electronegativity, electrolysis, experimental aspects of strontianite, halide test, evaluation of present and future computer programs in chemistry, formula building, care of glass/saturated calomel…

  4. ENVIRONMENTAL CHEMISTRY

    EPA Science Inventory

    Environmental chemistry is applied to estimating the exposure of ecosystems and humans to various chemical environmental stressors. Among the stressors of concern are mercury, pesticides, and arsenic. Advanced analytical chemistry techniques are used to measure these stressors ...

  5. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1982

    1982-01-01

    Presents background information, laboratory procedures, classroom materials/activities, and experiments for chemistry. Topics include superheavy elements, polarizing power and chemistry of alkali metals, particulate carbon from combustion, tips for the chemistry laboratory, interesting/colorful experiments, behavior of bismuth (III) iodine, and…

  6. Crack formation and prevention in colloidal drops.

    PubMed

    Kim, Jin Young; Cho, Kun; Ryu, Seul-A; Kim, So Youn; Weon, Byung Mook

    2015-01-01

    Crack formation is a frequent result of residual stress release from colloidal films made by the evaporation of colloidal droplets containing nanoparticles. Crack prevention is a significant task in industrial applications such as painting and inkjet printing with colloidal nanoparticles. Here, we illustrate how colloidal drops evaporate and how crack generation is dependent on the particle size and initial volume fraction, through direct visualization of the individual colloids with confocal laser microscopy. To prevent crack formation, we suggest use of a versatile method to control the colloid-polymer interactions by mixing a nonadsorbing polymer with the colloidal suspension, which is known to drive gelation of the particles with short-range attraction. Gelation-driven crack prevention is a feasible and simple method to obtain crack-free, uniform coatings through drying-mediated assembly of colloidal nanoparticles. PMID:26279317

  7. Crack formation and prevention in colloidal drops

    NASA Astrophysics Data System (ADS)

    Kim, Jin Young; Cho, Kun; Ryu, Seul-A.; Kim, So Youn; Weon, Byung Mook

    2015-08-01

    Crack formation is a frequent result of residual stress release from colloidal films made by the evaporation of colloidal droplets containing nanoparticles. Crack prevention is a significant task in industrial applications such as painting and inkjet printing with colloidal nanoparticles. Here, we illustrate how colloidal drops evaporate and how crack generation is dependent on the particle size and initial volume fraction, through direct visualization of the individual colloids with confocal laser microscopy. To prevent crack formation, we suggest use of a versatile method to control the colloid-polymer interactions by mixing a nonadsorbing polymer with the colloidal suspension, which is known to drive gelation of the particles with short-range attraction. Gelation-driven crack prevention is a feasible and simple method to obtain crack-free, uniform coatings through drying-mediated assembly of colloidal nanoparticles.

  8. Crack formation and prevention in colloidal drops

    PubMed Central

    Kim, Jin Young; Cho, Kun; Ryu, Seul-a; Kim, So Youn; Weon, Byung Mook

    2015-01-01

    Crack formation is a frequent result of residual stress release from colloidal films made by the evaporation of colloidal droplets containing nanoparticles. Crack prevention is a significant task in industrial applications such as painting and inkjet printing with colloidal nanoparticles. Here, we illustrate how colloidal drops evaporate and how crack generation is dependent on the particle size and initial volume fraction, through direct visualization of the individual colloids with confocal laser microscopy. To prevent crack formation, we suggest use of a versatile method to control the colloid-polymer interactions by mixing a nonadsorbing polymer with the colloidal suspension, which is known to drive gelation of the particles with short-range attraction. Gelation-driven crack prevention is a feasible and simple method to obtain crack-free, uniform coatings through drying-mediated assembly of colloidal nanoparticles. PMID:26279317

  9. Entropy favours open colloidal lattices

    NASA Astrophysics Data System (ADS)

    Mao, Xiaoming; Chen, Qian; Granick, Steve

    2013-03-01

    Burgeoning experimental and simulation activity seeks to understand the existence of self-assembled colloidal structures that are not close-packed. Here we describe an analytical theory based on lattice dynamics and supported by experiments that reveals the fundamental role entropy can play in stabilizing open lattices. The entropy we consider is associated with the rotational and vibrational modes unique to colloids interacting through extended attractive patches. The theory makes predictions of the implied temperature, pressure and patch-size dependence of the phase diagram of open and close-packed structures. More generally, it provides guidance for the conditions at which targeted patchy colloidal assemblies in two and three dimensions are stable, thus overcoming the difficulty in exploring by experiment or simulation the full range of conceivable parameters.

  10. Doped colloidal artificial spin ice

    NASA Astrophysics Data System (ADS)

    Libál, A.; Olson Reichhardt, C. J.; Reichhardt, C.

    2015-10-01

    We examine square and kagome artificial spin ice for colloids confined in arrays of double-well traps. Unlike magnetic artificial spin ices, colloidal and vortex artificial spin ice realizations allow creation of doping sites through double occupation of individual traps. We find that doping square and kagome ice geometries produces opposite effects. For square ice, doping creates local excitations in the ground state configuration that produce a local melting effect as the temperature is raised. In contrast, the kagome ice ground state can absorb the doping charge without generating non-ground-state excitations, while at elevated temperatures the hopping of individual colloids is suppressed near the doping sites. These results indicate that in the square ice, doping adds degeneracy to the ordered ground state and creates local weak spots, while in the kagome ice, which has a highly degenerate ground state, doping locally decreases the degeneracy and creates local hard regions.

  11. Polymeric stabilization of colloidal asphaltenes

    NASA Astrophysics Data System (ADS)

    Hashmi, Sara; Firoozabadi, Abbas

    2010-03-01

    Asphaltenes, the heaviest component of crude oil, cause many problems in petroleum extraction and recovery. Operationally defined as insoluble in long chain alkanes but soluble in toluene, asphaltenes have been described by bulk thermodynamic models such as the Flory-Huggins theory. However, bulk models work well only for asphaltenes in good solvents. Characterization of asphaltenes in poor solvents remains elusive: molecular scale asphaltenes readily aggregate to the colloidal scale and become highly unstable in solution. We investigate the ability of polymers to stabilize colloidal asphaltene suspensions in heptane. In the absence of added polymer, sedimentation measurements reveal dynamics reminiscent of collapsing gels. Adding polymers to colloidal asphaltene suspensions can delay the characteristic sedimentation time by orders of magnitude. Light scattering results suggest that the mechanism of stabilization may be related to a decrease in both particle size and polydispersity as a function of added polymer.

  12. Gel transitions in colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Bergenholtz, J.; Fuchs, M.

    1999-12-01

    The idealized mode-coupling theory (MCT) is applied to colloidal systems interacting via short-range attractive interactions of Yukawa form. At low temperatures, MCT predicts a slowing down of the local dynamics and ergodicity-breaking transitions. The non-ergodicity transitions share many features with the colloidal gel transition, and are proposed to be the source of gelation in colloidal systems. Previous calculations of the phase diagram are complemented with additional data for shorter ranges of the attractive interaction, showing that the path of the non-ergodicity transition line is then unimpeded by the gas-liquid critical curve at low temperatures. Particular attention is given to the critical non-ergodicity parameters; this is motivated by recent experimental measurements. An asymptotic model is developed, valid for dilute systems of spheres interacting via strong short-range attractions, and is shown to capture all aspects of the low-temperature MCT non-ergodicity transitions.

  13. Colloidal particle assembly using piezoelectric inkjet printing of polystyrene colloidal ink formulations.

    PubMed

    Kwon, Younghwan

    2014-10-01

    We report the feasibility of piezoelectric inkjet printing of colloidal dispersion inks for geometrical patterning to arrange colloids in desired locations. Polystyrene colloid (dia. = 3 μm) inks dispersed with thermally curable binder in organic solvents are explored for fundamental study on colloidal patterning. The inkjet printability of colloidal inks is systematically investigated with different ink formulations and inkjet process variables. In addition, in order to maintain the structural stability of colloidal patterns fabricated on the substrate from externally applied forces such as mechanical, chemical and thermal stimuli, thermally curable binder was formulated into the colloidal ink formulations. PMID:25942838

  14. Colloid cyst: a case report.

    PubMed

    Grasu, Beatrice L; Alberico, Anthony M

    2011-01-01

    Colloid cysts are a rare clinical finding with a unique clinical presentation: non-specific paroxysmal headaches. The current recommended treatment is microsurgery, which poses the greatest risk to the patient but allows complete removal of the cyst to prevent recurrence. A 41-year old man presented with a colloid cyst located in the foramen of Monro causing obstructive hydrocephalus. He had paroxysmal headaches and memory and personality changes. Transcortical transventricle microsurgery was performed to remove the entire cyst. A temporary shunt was placed to prevent post-operative hydrocephalus. Normal neurological function returned upon cyst removal. PMID:22034805

  15. CLUSTER CHEMISTRY

    SciTech Connect

    Muetterties, Earl L.

    1980-05-01

    Metal cluster chemistry is one of the most rapidly developing areas of inorganic and organometallic chemistry. Prior to 1960 only a few metal clusters were well characterized. However, shortly after the early development of boron cluster chemistry, the field of metal cluster chemistry began to grow at a very rapid rate and a structural and a qualitative theoretical understanding of clusters came quickly. Analyzed here is the chemistry and the general significance of clusters with particular emphasis on the cluster research within my group. The importance of coordinately unsaturated, very reactive metal clusters is the major subject of discussion.

  16. Forensic Chemistry

    NASA Astrophysics Data System (ADS)

    Bell, Suzanne

    2009-07-01

    Forensic chemistry is unique among chemical sciences in that its research, practice, and presentation must meet the needs of both the scientific and the legal communities. As such, forensic chemistry research is applied and derivative by nature and design, and it emphasizes metrology (the science of measurement) and validation. Forensic chemistry has moved away from its analytical roots and is incorporating a broader spectrum of chemical sciences. Existing forensic practices are being revisited as the purview of forensic chemistry extends outward from drug analysis and toxicology into such diverse areas as combustion chemistry, materials science, and pattern evidence.

  17. Colloids and Nucleation

    NASA Technical Reports Server (NTRS)

    Ackerson, Bruce

    1997-01-01

    The objectives of the work funded under this grant were to develop a microphotographic technique and use it to monitor the nucleation and growth of crystals of hard colloidal spheres. Special attention is given to the possible need for microgravity studies in future experiments. A number of persons have been involved in this work. A masters student, Keith Davis, began the project and developed a sheet illumination apparatus and an image processing system for detection and analysis. His work on a segmentation program for image processing was sufficient for his master's research and has been published. A post doctoral student Bernie Olivier and a graduate student Yueming He, who originally suggested the sheet illumination, were funded by another source but along with Keith made photographic series of several samples (that had been made by Keith Davis). Data extraction has been done by Keith, Bernie, Yueming and two undergraduates employed on the grant. Results are published in Langmuir. These results describe the sheet lighting technique as one which illuminates not only the Bragg scattering crystal, but all the crystals. Thus, accurate crystal counts can be made for nucleation rate measurements. The strange crystal length scale reduction, observed in small angle light scattering (SALS) studies, following the initial nucleation and growth period, has been observed directly. The Bragg scattering (and dark) crystal size decreases in the crossover region. This could be an effect due to gravitational forces or due to over- compression of the crystal during growth. Direct observations indicate a complex morphology for the resulting hard sphere crystals. The crystal edges are fairly sharp but the crystals have a large degree of internal structure. This structure is a result of (unstable) growth and not aggregation. As yet unpublished work compares growth exponents data with data obtained by SALS. The nucleation rate density is determined over a broad volume fraction range

  18. Influences of Flow Transients and Porous Medium Heterogeneity on Colloid-Associated Contaminant Transport in the Vadose Zone

    SciTech Connect

    Saiers, James; Ryan, Joseph

    2005-06-01

    Our research is guided by an EMSP objective to improve conceptual and predictive models of contaminant movement in vadose-zone environments. As described in the report National Roadmap for Vadose-Zone Science and Technology [DOE, 2001], soil-water colloids are capable of adsorbing contaminants, such as radionuclides and metals, and facilitating their migration through the vadose zone and towards groundwater reservoirs. Our research centers on advancing understanding of this phenomenon. In particular, we are combining mathematical modeling with laboratory experimentation at pore and column scales to (1) elucidate the effects of porewater-flow transients on colloid mobilization in unsaturated porous media; (2) explore the sensitivity of colloid deposition rates to changes in porewater chemistry and colloid mineralogy; (3) develop mathematical models appropriate for simulating colloid mobilization, transport, and deposition under both steady-flow and transient-flow conditions; (4) identify mechanisms that govern mineral-colloid mobilization and deposition in unsaturated porous media; (5) quantify the effects of mineral-grain geometry and surface roughness on colloid-filtration rates; and (6) evaluate the influences of colloids on the transport of strontium and cesium (i.e., DOE-contaminants-of-concern) through soils and sediments.

  19. Defect Chemistry and Plasmon Physics of Colloidal Metal Oxide Nanocrystals

    SciTech Connect

    Lounis, SD; Runnerstrorm, EL; Llordes, A; Milliron, DJ

    2014-05-01

    Plasmonic nanocrystals of highly doped metal oxides have seen rapid development in the past decade and represent a class of materials with unique optoelectronic properties. In this Perspective, we discuss doping mechanisms in metal oxides and the accompanying physics of free carrier scattering, both of which have implications in determining the properties of localized surface plasmon resonances (LSPRs) in these nanocrystals. The balance between activation and compensation of dopants limits the free carrier concentration of the most common metal oxides, placing a ceiling on the LSPR frequency. Furthermore, because of ionized impurity scattering of the oscillating plasma by dopant ions, scattering must be treated in a fundamentally different way in semiconductor metal oxide materials when compared with conventional metals. Though these effects are well-understood in bulk metal oxides, further study is needed to understand their manifestation in nanocrystals and corresponding impact on plasmonic properties, and to develop materials that surpass current limitations in free carrier concentration.

  20. Colloid characterization and quantification in groundwater samples

    SciTech Connect

    K. Stephen Kung

    2000-06-01

    This report describes the work conducted at Los Alamos National Laboratory for studying the groundwater colloids for the Yucca Mountain Project in conjunction with the Hydrologic Resources Management Program (HRMP) and the Underground Test Area (UGTA) Project. Colloidal particle size distributions and total particle concentration in groundwater samples are quantified and characterized. Colloid materials from cavity waters collected near underground nuclear explosion sites by HRMP field sampling personnel at the Nevada Test Site (NTS) were quantified. Selected colloid samples were further characterized by electron microscope to evaluate the colloid shapes, elemental compositions, and mineral phases. The authors have evaluated the colloid size and concentration in the natural groundwater sample that was collected from the ER-20-5 well and stored in a 50-gallon (about 200-liter) barrel for several months. This groundwater sample was studied because HRMP personnel have identified trace levels of radionuclides in the water sample. Colloid results show that even though the water sample had filtered through a series of Millipore filters, high-colloid concentrations were identified in all unfiltered and filtered samples. They had studied the samples that were diluted with distilled water and found that diluted samples contained more colloids than the undiluted ones. These results imply that colloids are probably not stable during the storage conditions. Furthermore, results demonstrate that undesired colloids have been introduced into the samples during the storage, filtration, and dilution processes. They have evaluated possible sources of colloid contamination associated with sample collection, filtrating, storage, and analyses of natural groundwaters. The effects of container types and sample storage time on colloid size distribution and total concentration were studied to evaluate colloid stability by using J13 groundwater. The data suggests that groundwater samples

  1. Microbial effects on colloidal agglomeration

    SciTech Connect

    Hersman, L.

    1995-11-01

    Colloidal particles are known to enhance the transport of radioactive metals through soil and rock systems. This study was performed to determine if a soil microorganism, isolated from the surface samples collected at Yucca Mountain, NV, could affect the colloidal properties of day particles. The agglomeration of a Wyoming bentonite clay in a sterile uninoculated microbial growth medium was compared to the agglomeration in the medium inoculated with a Pseudomonas sp. In a second experiment, microorganisms were cultured in the succinate medium for 50 h and removed by centrifugation. The agglomeration of the clay in this spent was compared to sterile uninoculated medium. In both experiments, the agglomeration of the clay was greater than that of the sterile, uninoculated control. Based on these results, which indicate that this microorganism enhanced the agglomeration of the bentonite clay, it is possible to say that in the presence of microorganisms colloidal movement through a rock matrix could be reduced because of an overall increase in the size of colloidal particle agglomerates. 32 refs.

  2. Solid colloidal optical wavelength filter

    DOEpatents

    Alvarez, Joseph L.

    1992-01-01

    A solid colloidal optical wavelength filter includes a suspension of spheal particles dispersed in a coagulable medium such as a setting plastic. The filter is formed by suspending spherical particles in a coagulable medium; agitating the particles and coagulable medium to produce an emulsion of particles suspended in the coagulable medium; and allowing the coagulable medium and suspended emulsion of particles to cool.

  3. Sonochemical synthesis of iron colloids

    SciTech Connect

    Suslick, K.S.; Fang, M.; Hyeon, T.

    1996-11-27

    We present here a new method for the preparation of stable ferromagnetic colloids of iron using high-intensity ultrasound to sonochemically decompose volatile organometallic compounds. These colloids have narrow size distributions centered at a few nanometers and are found to be superparamagnetic. In conclusion, a simple synthetic method has been discovered to produce nanosized iron colloid using high-intensity ultrasound. Nanometer iron particles dispersed in polyvinylpyrrolidone (PVP) matrix or stabilized by adsorption of oleic acid have been synthesized by sonochemical decomposition of Fe(CO){sub 5}. Transmission electron micrographs show that the iron particles have a relatively narrow range in size from 3 to 8 nm for polyvinylpyrrolidone, while oleic acid gives an even more uniform distribution at 8 nm. magnetic measurements revealed that these nanometer iron particles are superparamagnetic with a saturation magnetization of 101 emu/g (Fe) at 290 K. This work is easily extended to colloids of other metals and to alloys of two or more metals, simply by using multiple volatile precursors. 29 refs., 4 figs.

  4. Physics of Colloids in Space

    NASA Technical Reports Server (NTRS)

    Weitz, Dave; Weeks, Eric; Gasser, Urs; Dinsmore, Tony; Mawley, Suliana; Segre, Phil; Cipelletti, Lucia

    2000-01-01

    This talk will present recent results from ground-based research to support the "Physics of Colloids in Space" project which is scheduled to fly in the ISS approximately one year from now. In addition, results supporting future planned flights will be discussed.

  5. Dynamics of evaporative colloidal patterning

    NASA Astrophysics Data System (ADS)

    Kaplan, C. Nadir; Wu, Ning; Mandre, Shreyas; Aizenberg, Joanna; Mahadevan, L.

    2015-09-01

    Drying suspensions often leave behind complex patterns of particulates, as might be seen in the coffee stains on a table. Here, we consider the dynamics of periodic band or uniform solid film formation on a vertical plate suspended partially in a drying colloidal solution. Direct observations allow us to visualize the dynamics of band and film deposition, where both are made of multiple layers of close packed particles. We further see that there is a transition between banding and filming when the colloidal concentration is varied. A minimal theory of the liquid meniscus motion along the plate reveals the dynamics of the banding and its transition to the filming as a function of the ratio of deposition and evaporation rates. We also provide a complementary multiphase model of colloids dissolved in the liquid, which couples the inhomogeneous evaporation at the evolving meniscus to the fluid and particulate flows and the transition from a dilute suspension to a porous plug. This allows us to determine the concentration dependence of the bandwidth and the deposition rate. Together, our findings allow for the control of drying-induced patterning as a function of the colloidal concentration and evaporation rate.

  6. Towards Structural Complexity with Colloids

    NASA Astrophysics Data System (ADS)

    Engel, Michael

    2012-02-01

    Colloids rather easily assemble into simple crystal structures like the face-centered cubic lattice or the body-centered cubic lattice. More complex phases are harder to achieve, but have recently been reported using a number of approaches. Yet, assembling complex structures often results from trial-and-error and is not well understood. In this presentation, we show how novel crystals, quasicrystals, and liquid crystals can be achieved with colloidal building blocks by varying the interactions and the shapes of the building blocks. Using computer simulations, we demonstrate the formation of unusually ordered phases both with isotropic pair potentials, as well as with facetted shapes like polyhedra. We describe new tools we have developed to perform complex structural analysis on simulated systems and show how they may be used to analyze real space images from colloid experiments. We also compare the assembled structures with densest packings of the building blocks and show that good packings can often be distinct from what is observed to assemble from the disordered state. This suggests that dense packings may not be illustrative of what is achievable in colloid experiments.

  7. Surface-modified silica colloidal crystals: nanoporous films and membranes with controlled ionic and molecular transport.

    PubMed

    Zharov, Ilya; Khabibullin, Amir

    2014-02-18

    Nanoporous membranes are important for the study of the transport of small molecules and macromolecules through confined spaces and in applications ranging from separation of biomacromolecules and pharmaceuticals to sensing and controlled release of drugs. For many of these applications, chemists need to gate the ionic and molecular flux through the nanopores, which in turn depends on the ability to control the nanopore geometry and surface chemistry. Most commonly used nanoporous membrane materials are based on polymers. However, the nanostructure of polymeric membranes is not well-defined, and their surface is hard to modify. Inorganic nanoporous materials are attractive alternatives for polymers in the preparation of nanoporous membranes. In this Account, we describe the preparation and surface modification of inorganic nanoporous films and membranes self-assembled from silica colloidal spheres. These spheres form colloidal crystals with close-packed face centered cubic lattices upon vertical deposition from colloidal solutions. Silica colloidal crystals contain ordered arrays of interconnected three dimensional voids, which function as nanopores. We can prepare silica colloidal crystals as supported thin films on various flat solid surfaces or obtain free-standing silica colloidal membranes by sintering the colloidal crystals above 1000 °C. Unmodified silica colloidal membranes are capable of size-selective separation of macromolecules, and we can surface-modify them in a well-defined and controlled manner with small molecules and polymers. For the surface modification with small molecules, we use silanol chemistry. We grow polymer brushes with narrow molecular weight distribution and controlled length on the colloidal nanopore surface using atom transfer radical polymerization or ring-opening polymerization. We can control the flux in the resulting surface-modified nanoporous films and membranes by pH and ionic strength, temperature, light, and small molecule

  8. Effective Forces Between Colloidal Particles

    NASA Technical Reports Server (NTRS)

    Tehver, Riina; Banavar, Jayanth R.; Koplik, Joel

    1999-01-01

    Colloidal suspensions have proven to be excellent model systems for the study of condensed matter and its phase behavior. Many of the properties of colloidal suspensions can be investigated with a systematic variation of the characteristics of the systems and, in addition, the energy, length and time scales associated with them allow for experimental probing of otherwise inaccessible regimes. The latter property also makes colloidal systems vulnerable to external influences such as gravity. Experiments performed in micro-ravity by Chaikin and Russell have been invaluable in extracting the true behavior of the systems without an external field. Weitz and Pusey intend to use mixtures of colloidal particles with additives such as polymers to induce aggregation and form weak, tenuous, highly disordered fractal structures that would be stable in the absence of gravitational forces. When dispersed in a polarizable medium, colloidal particles can ionize, emitting counterions into the solution. The standard interaction potential in these charged colloidal suspensions was first obtained by Derjaguin, Landau, Verwey and Overbeek. The DLVO potential is obtained in the mean-field linearized Poisson-Boltzmann approximation and thus has limited applicability. For more precise calculations, we have used ab initio density functional theory. In our model, colloidal particles are charged hard spheres, the counterions are described by a continuum density field and the solvent is treated as a homogeneous medium with a specified dielectric constant. We calculate the effective forces between charged colloidal particles by integrating over the solvent and counterion degrees of freedom, taking into account the direct interactions between the particles as well as particle-counterion, counterion-counterion Coulomb, counterion entropic and correlation contributions. We obtain the effective interaction potential between charged colloidal particles in different configurations. We evaluate two

  9. Selenium Redox Reactivity on Colloidal CdSe Quantum Dot Surfaces

    PubMed Central

    2016-01-01

    Understanding the structural and compositional origins of midgap states in semiconductor nanocrystals is a longstanding challenge in nanoscience. Here, we report a broad variety of reagents useful for photochemical reduction of colloidal CdSe quantum dots, and we establish that these reactions proceed via a dark surface prereduction step prior to photoexcitation. Mechanistic studies relying on the specific properties of various reductants lead to the proposal that this surface prereduction occurs at oxidized surface selenium sites. These results demonstrate the use of small-molecule inorganic chemistries to control the physical properties of colloidal QDs and provide microscopic insights into the identities and reactivities of their localized surface species. PMID:27518320

  10. Like-charge interactions between colloidal particles are asymmetric with respect to sign†

    PubMed Central

    Gomez, Esther W.; Clack, Nathan G.; Wu, Hung-Jen; Groves, Jay T.

    2014-01-01

    Two-dimensional dispersions of colloidal particles with a range of surface chemistries and electrostatic potentials are characterized under a series of solution ionic strengths. A combination of optical imaging techniques are employed to monitor both the colloid structure and the electrostatic surface potential of individual particles in situ. We find that like-charge multiparticle interactions can be tuned from exclusively repulsive to long-range attractive by changing the particle surface composition. This behavior is strongly asymmetric with respect to the sign of the surface potential. Collective long-range attractive interactions are only observed among negatively charged particles. PMID:25221611

  11. Selenium Redox Reactivity on Colloidal CdSe Quantum Dot Surfaces.

    PubMed

    Tsui, Emily Y; Hartstein, Kimberly H; Gamelin, Daniel R

    2016-09-01

    Understanding the structural and compositional origins of midgap states in semiconductor nanocrystals is a longstanding challenge in nanoscience. Here, we report a broad variety of reagents useful for photochemical reduction of colloidal CdSe quantum dots, and we establish that these reactions proceed via a dark surface prereduction step prior to photoexcitation. Mechanistic studies relying on the specific properties of various reductants lead to the proposal that this surface prereduction occurs at oxidized surface selenium sites. These results demonstrate the use of small-molecule inorganic chemistries to control the physical properties of colloidal QDs and provide microscopic insights into the identities and reactivities of their localized surface species. PMID:27518320

  12. Distorted colloidal arrays as designed template

    NASA Astrophysics Data System (ADS)

    Yu, Ye; Zhou, Ziwei; Möhwald, Helmuth; Ai, Bin; Zhao, Zhiyuan; Ye, Shunsheng; Zhang, Gang

    2015-01-01

    In this paper, a novel type of colloidal template with broken symmetry was generated using commercial, inductively coupled plasma reactive ion etching (ICP-RIE). With proper but simple treatment, the traditional symmetric non-close-packed colloidal template evolves into an elliptical profile with high uniformity. This unique feature can add flexibility to colloidal lithography and/or other lithography techniques using colloidal particles as building blocks to fabricate nano-/micro-structures with broken symmetry. Beyond that the novel colloidal template we developed possesses on-site tunability, i.e. the transformability from a symmetric into an asymmetric template. Sandwich-type particles with eccentric features were fabricated utilizing this tunable template. This distinguishing feature will provide the possibility to fabricate structures with unique asymmetric features using one set of colloidal template, providing flexibility and broad tunability to enable nano-/micro-structure fabrication with colloidal templates.

  13. Glass/Jamming Transition in Colloidal Aggregation

    NASA Technical Reports Server (NTRS)

    Segre, Philip N.; Prasad, Vikram; Weitz, David A.; Rose, M. Franklin (Technical Monitor)

    2000-01-01

    We have studied colloidal aggregation in a model colloid plus polymer system with short-range attractive interactions. By varying the colloid concentration and the strength of the attraction, we explored regions where the equilibrium phase is expected to consist of colloidal crystallites in coexistance with colloidal gas (i.e. monomers). This occurs for moderate values of the potential depth, U approximately equal to 2-5 kT. Crystallization was not always observed. Rather, over an extended sub-region two new metastable phases appear, one fluid-like and one solid-like. These were examined in detail with light scattering and microscopy techniques. Both phases consist of a near uniform distribution of small irregular shaped clusters of colloidal particles. The dynamical and structural characteristics of the ergodic-nonergodic transition between the two phases share much in common with the colloidal hard sphere glass transition.

  14. Colloid particle size-dependent dispersivity

    NASA Astrophysics Data System (ADS)

    Chrysikopoulos, C. V.; Katzourakis, V. E.

    2014-12-01

    Laboratory and field studies have demonstrated that dispersion coefficients evaluated by fitting advection-dispersion transport models to nonreactive tracer breakthrough curves do not adequately describe colloid transport under the same flow field conditions. Here an extensive laboratory study was undertaken to assess whether the dispersivity, which traditionally has been considered to be a property of the porous medium, is dependent on colloid particle size and interstitial velocity. A total of 49 colloid transport experiments were performed in columns packed with glass beads under chemically unfavorable colloid attachment conditions. Nine different colloid diameters, and various flow velocities were examined. The breakthrough curves were successfully simulated with a mathematical model describing colloid transport in homogeneous, water saturated porous media. The results demonstrated that the dispersivity is positively correlated with colloid particle size, and increases with increasing velocity.

  15. CHARACTERIZATION OF SUB-MICRON AQUEOUS IRON(III) COLLOIDS FORMED IN THE PRESENCE OF PHOSPHATE BY SEDIMENTATION FIELD FLOW FRACTIONATION WITH MULTI-ANGLE LASER LIGHT SCATTERING DETECTION

    EPA Science Inventory

    Iron colloids play a major role in the water chemistry of natural watersheds and of engineered drinking water distribution systems. Phosphate is frequently added to distribution systems to control corrosion problems, so iron-phosphate colloids may form through reaction of iron in...

  16. Impact of dissolved organic matter on colloid transport in the vadose zone: deterministic approximation of transport deposition coefficients from polymeric coating characteristics.

    PubMed

    Morales, Verónica L; Zhang, Wei; Gao, Bin; Lion, Leonard W; Bisogni, James J; McDonough, Brendan A; Steenhuis, Tammo S

    2011-02-01

    Although numerous studies have been conducted to discern colloid transport and stability processes, the mechanistic understanding of how dissolved organic matter (DOM) affects colloid fate in unsaturated soils (i.e., the vadose zone) remains unclear. This study aims to bridge the gap between the physicochemical responses of colloid complexes and porous media interfaces to solution chemistry, and the effect these changes have on colloid transport and fate. Measurements of adsorbed layer thickness, density, and charge of DOM-colloid complexes and transport experiments with tandem internal process visualization were conducted for key constituents of DOM, humic (HA) and fulvic acids (FA), at acidic, neutral and basic pH and two CaCl(2) concentrations. Polymeric characteristics reveal that, of the two tested DOM constituents, only HA electrosterically stabilizes colloids. This stabilization is highly dependent on solution pH which controls DOM polymer adsorption affinity, and on the presence of Ca(+2) which promotes charge neutralization and inter-particle bridging. Transport experiments indicate that HA improved colloid transport significantly, while FA only marginally affected transport despite having a large effect on particle charge. A transport model with deposition and pore-exclusion parameters fit experimental breakthrough curves well. Trends in deposition coefficients are correlated to the changes in colloid surface potential for bare colloids, but must include adsorbed layer thickness and density for sterically stabilized colloids. Additionally, internal process observations with bright field microscopy reveal that, under optimal conditions for retention, experiments with FA or no DOM promoted colloid retention at solid-water interfaces, while experiments with HA enhanced colloid retention at air-water interfaces, presumably due to partitioning of HA at the air-water interface and/or increased hydrophobic characteristics of HA-colloid complexes. PMID:21193215

  17. Surface-Enhanced Resonance Raman Scattering and Visible Extinction Spectroscopy of Copper Chlorophyllin: An Upper Level Chemistry Experiment

    ERIC Educational Resources Information Center

    Schnitzer, Cheryl S.; Reim, Candace Lawson; Sirois, John J.; House, Paul G.

    2010-01-01

    Advanced chemistry students are introduced to surface-enhanced resonance Raman scattering (SERRS) by studying how sodium copper chlorophyllin (CuChl) adsorbs onto silver colloids (CuChl/Ag) as a function of pH. Using both SERRS and visible extinction spectroscopy, the extent of CuChl adsorption and colloidal aggregation are monitored. Initially at…

  18. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1972

    1972-01-01

    Twelve new chemistry expermiments are described. Broad areas covered include atomic structure, solubility, gaseous diffusion, endothermic reactions, alcohols, equilibrium, atomic volumes, and some improvised apparatus. (PS)

  19. Technetium chemistry

    SciTech Connect

    Burns, C.; Bryan, J.; Cotton, F.; Ott, K.; Kubas, G.; Haefner, S.; Barrera, J.; Hall, K.; Burrell, A.

    1996-04-01

    Technetium chemistry is a young and developing field. Despite the limited knowledge of its chemistry, technetium is the workhorse for nuclear medicine. Technetium is also a significant environmental concern because it is formed as a byproduct of nuclear weapons production and fission-power generators. Development of new technetium radio-pharmaceuticals and effective environmental control depends strongly upon knowledge of basic technetium chemistry. The authors performed research into the basic coordination and organometallic chemistry of technetium and used this knowledge to address nuclear medicine and environmental applications. This is the final report of a three-year Laboratory-Directed Research and Development (LDRD) project at the Los Alamos National Laboratory (LANL).

  20. Colloidal aspects of texture perception.

    PubMed

    van Vliet, Ton; van Aken, George A; de Jongh, Harmen H J; Hamer, Rob J

    2009-08-30

    Recently, considerable attention has been given to the understanding of texture attributes that cannot directly be related to physical properties of food, such as creamy, crumbly and watery. The perception of these attributes is strongly related to the way the food is processed during food intake, mastication, swallowing of it and during the cleaning of the mouth after swallowing. Moreover, their perception is modulated by the interaction with other basic attributes, such as taste and aroma attributes (e.g. sourness and vanilla). To be able to link the composition and structure of food products to more complicated texture attributes, their initial physical/colloid chemical properties and the oral processing of these products must be well understood. Understanding of the processes in the mouth at colloidal length scales turned out to be essential to grasp the interplay between perception, oral physiology and food properties. In view of the huge differences in physical chemical properties between food products, it is practical to make a distinction between solid, semi-solid, and liquid food products. The latter ones are often liquid dispersions of emulsion droplets or particles in general. For liquid food products for instance flow behaviour and colloidal stability of dispersed particles play a main role in determining their textural properties. For most solid products stiffness and fracture behaviour in relation to water content are essential while for semi-solids a much larger range of mechanical properties will play a role. Examples of colloidal aspects of texture perception will be discussed for these three categories of products based on selected sensory attributes and/or relevant colloidal processes. For solid products some main factors determining crispness will be discussed. For crispiness of dry cellular solid products these are water content and the architecture of the product at mesoscopic length scales (20-1000 microm). In addition the distribution of

  1. Statistical Physics of Colloidal Dispersions.

    NASA Astrophysics Data System (ADS)

    Canessa, E.

    Available from UMI in association with The British Library. Requires signed TDF. This thesis is concerned with the equilibrium statistical mechanics of colloidal dispersions which represent useful model systems for the study of condensed matter physics; namely, charge stabilized colloidal dispersions and polymer stabilized colloidal dispersions. A one-component macroparticle approach is adopted in order to treat the macroscopic and microscopic properties of these systems in a simple and comprehensive manner. The thesis opens with the description of the nature of the colloidal state before reviewing some basic definitions and theory in Chapter II. In Chapter III a variational theory of phase equilibria based on the Gibbs-Bogolyobov inequality is applied to sterically stabilized colloidal dispersions. Hard spheres are chosen as the reference system for the disordered phases while an Einstein model is used for the ordered phases. The new choice of pair potential, taken for mathematical convenience, is a superposition of two Yukawa functions. By matching a double Yukawa potential to the van der Waals attractive potential at different temperatures and introducing a purely temperature dependent coefficient to the repulsive part, a rich variety of observed phase separation phenomena is qualitatively described. The behaviour of the potential is found to be consistent with a small decrease of the polymer layer thickness with increasing temperature. Using the same concept of a collapse transition the non-monotonic second virial coefficient is also explained and quantified. It is shown that a reduction of the effective macroparticle diameter with increasing temperature can only be partially examined from the point of view of a (binary-) polymer solution theory. This chapter concludes with the description of the observed, reversible, depletion flocculation behaviour. This is accomplished by using the variational formalism and by invoking the double Yukawa potential to allow

  2. What happens when pharmaceuticals meet colloids.

    PubMed

    Xing, Yingna; Chen, Xijuan; Zhuang, Jie; Chen, Xin

    2015-12-01

    Pharmaceuticals (PCs) have been widely detected in natural environment due to agricultural application of reclaimed water, sludge and animal wastes. Their potential risks to various ecosystems and even to human health have caused great concern; however, little was known about their environmental behaviors. Colloids (such as clays, metal oxides, and particulate organics) are kind of substances that are active and widespread in the environment. When PCs meet colloids, their interaction may influence the fate, transport, and toxicity of PCs. This review summarizes the progress of studies on the role of colloids in mediating the environmental behaviors of PCs. Synthesized results showed that colloids can adsorb PCs mainly through ion exchange, complexation and non-electrostatic interactions. During this process the structure of colloids and the stability of PCs may be changed. The adsorbed PCs may have higher risks to induce antibiotic resistance; besides, their transport may also be altered considering they have great chance to move with colloids. Solution conditions (such as pH, ionic strength, and cations) could influence these interactions between PCs and colloids, as they can change the forms of PCs and alter the primary forces between PCs and colloids in the solution. It could be concluded that PCs in natural soils could bind with colloids and then co-transport during the processes of irrigation, leaching, and erosion. Therefore, colloid-PC interactions need to be understood for risk assessment of PCs and the best management practices of various ecosystems (such as agricultural and wetland systems). PMID:26427370

  3. Preparatiion of metal colloids in inverse micelles

    SciTech Connect

    Wilcoxon, J.P.

    1990-11-23

    A method is provided for preparing catalytic elemental metal colloidal particles (e.g., gold, palladium, silver, rhodium, nickel, iron, platinum, molybdenum) or colloidal alloy particles (silver/iridium or platinum/gold). A homogenous inverse micelle solution of a metal salt is first formed in a metal-salt solvent comprised of a surfactant (e.g. a nonionic or cationic surfactant) and an organic solvent. The size and number of inverse micelles is controlled by the proportions of the surfactant and the solvent. Then, the metal salt is reduced (by chemical reduction or by a pulsed or continuous wave UV laser) to colloidal particles of elemental metal. After their formation, the colloidal metal particles can be stabilized by reaction with materials that permanently add surface stabilizing groups to the surface of the colloidal metal particles. The sizes of the colloidal elemental metal particles and their size distribution is determined by the size and number of the inverse micelles. A second salt can be added with further reduction to form the colloidal alloy particles. After the colloidal elemental metal particles are formed, the homogeneous solution distributes to two phases, one phase rich in colloidal elemental metal particles and the other phase rich in surfactant. The colloidal elemental metal particles from one phase can be dried to form a powder useful as a catalyst.

  4. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1981

    1981-01-01

    Outlines laboratory procedures, demonstrations, teaching suggestions, and content information related to chemistry. Topics include polarizing power; calorimetry and momentum; microcomputers in school chemistry; a constant-volume dispenser for liquids, floating magnets, and crystal lattices; preparation of chromium; and solvent polarity and…

  5. Chancellor Water Colloids: Characterization and Radionuclide Association

    SciTech Connect

    Abdel-Fattah, Amr I.

    2012-06-18

    Concluding remarks about this paper are: (1) Gravitational settling, zeta potential, and ultrafiltration data indicate the existence of a colloidal phase of both the alpha and beta emitters in the Chancellor water; (2) The low activity combined with high dispersion homogeneity of the Chancellor water indicate that both alpha and beta emitters are not intrinsic colloids; (3) Radionuclides in the Chancellor water, particularly Pu, coexist as dissolved aqueous and sorbed phases - in other words the radionuclides are partitioned between the aqueous phase and the colloidal phase; (4) The presence of Pu as a dissolved species in the aqueous phase, suggests the possibility of Pu in the (V) oxidation state - this conclusion is supported by the similarity of the k{sub d} value of Pu determined in the current study to that determined for Pu(V) sorbed onto smectite colloids, and the similar electrokinetic behavior of the Chancellor water colloids to smectite colloids; (5) About 50% of the Pu(V) is in the aqueous phase and 50% is sorbed on colloids (mass concentration of colloids in the Chancellor water is 0.12 g/L); (6) The k{sub d} of the Pu and the beta emitters (fission products) between aqueous and colloidal phases in the Chancellor water is {approx}8.0 x 10{sup 3} mL/g using two different activity measurement techniques (LSC and alpha spectroscopy); (7) The gravitational settling and size distributions of the association colloids indicate that the properties (at least the physical ones) of the colloids to which the alpha emitters are associated with seem to be different that the properties of the colloids to which the beta emitters are associated with - the beta emitters are associated with very small particles ({approx}50 - 120 nm), while the alpha emitters are associated with relatively larger particles; and (8) The Chancellor water colloids are extremely stable under the natural pH and ionic strength conditions, indicating high potential for transport in the

  6. Electrokinetic properties of polymer colloids

    NASA Technical Reports Server (NTRS)

    Micale, F. J.; Fuenmayor, D. Y.

    1986-01-01

    The surface of polymer colloids, especially polystyrene latexes, were modified for the purpose of controlling the electrokinetic properties of the resulting colloids. Achievement required a knowledge of electrical double layer charging mechanism, as a function of the electrolyte conditions, at the polymer/water interface. The experimental approach is to control the recipe formulation in the emulsion polymerization process so as to systematically vary the strong acid group concentration on the surface of the polymer particles. The electrophoretic mobility of these model particles will then be measured as a function of surface group concentration and as a function of electrolyte concentration and type. An effort was also made to evaluate the electrophoretic mobility of polystyrene latexes made in space and to compare the results with latexes made on the ground.

  7. Predicting crystals of Janus colloids.

    PubMed

    Vissers, Teun; Preisler, Zdenek; Smallenburg, Frank; Dijkstra, Marjolein; Sciortino, Francesco

    2013-04-28

    We present a numerical study on the phase diagram for a simple model of Janus colloids, including ordered and disordered structures. Using a range of techniques, we generate a set of crystal structures and investigate their relative stability field in the pressure-temperature and temperature-density planes by means of free-energy calculations and thermodynamic integration schemes. We find that despite the Janus colloids' simple architecture, they form stable crystal structures with complicated bond-topologies on an underlying face-centered-cubic or hexagonal-close-packed lattice. In addition, we find a phase consisting of wrinkled bilayer sheets, competing with both the fluid and the crystal phases. We detect a metastable gas-liquid coexistence which displays a micellization-driven re-entrant behavior. PMID:23635155

  8. Magnetic Assisted Colloidal Pattern Formation

    NASA Astrophysics Data System (ADS)

    Yang, Ye

    Pattern formation is a mysterious phenomenon occurring at all scales in nature. The beauty of the resulting structures and myriad of resulting properties occurring in naturally forming patterns have attracted great interest from scientists and engineers. One of the most convenient experimental models for studying pattern formation are colloidal particle suspensions, which can be used both to explore condensed matter phenomena and as a powerful fabrication technique for forming advanced materials. In my thesis, I have focused on the study of colloidal patterns, which can be conveniently tracked in an optical microscope yet can also be thermally equilibrated on experimentally relevant time scales, allowing for ground states and transitions between them to be studied with optical tracking algorithms. In particular, I have focused on systems that spontaneously organize due to particle-surface and particle-particle interactions, paying close attention to systems that can be dynamically adjusted with an externally applied magnetic or acoustic field. In the early stages of my doctoral studies, I developed a magnetic field manipulation technique to quantify the adhesion force between particles and surfaces. This manipulation technique is based on the magnetic dipolar interactions between colloidal particles and their "image dipoles" that appear within planar substrate. Since the particles interact with their own images, this system enables massively parallel surface force measurements (>100 measurements) in a single experiment, and allows statistical properties of particle-surface adhesion energies to be extracted as a function of loading rate. With this approach, I was able to probe sub-picoNewton surface interactions between colloidal particles and several substrates at the lowest force loading rates ever achieved. In the later stages of my doctoral studies, I focused on studying patterns formed from particle-particle interaction, which serve as an experimental model of

  9. Phases transitions and interfaces in temperature-sensitive colloidal systems

    NASA Astrophysics Data System (ADS)

    Nguyen, Duc; Schall, Peter

    2013-03-01

    Colloids are widely used because of their exceptional properties. Beside their own applications in food, petrol, cosmetics and drug industries, photonic, optical filters and chemical sensor, they are also known as powerful model systems to study molecular phase behavior. Here, we examine both aspects of colloids using temperature-sensitive colloidal systems to fully investigate colloidal phase behavior and colloidal assembly.

  10. Colloidal metal oxide nanocrystal catalysis by sustained chemically driven ligand displacement

    NASA Astrophysics Data System (ADS)

    de Roo, Jonathan; van Driessche, Isabel; Martins, José C.; Hens, Zeger

    2016-05-01

    Surface chemistry is a key enabler for colloidal nanocrystal applications. In this respect, metal oxide nanocrystals (NCs) stand out from other NCs as carboxylic acid ligands adsorb on their surface by dissociation to carboxylates and protons, the latter proving essential in electron transfer reactions. Here, we show that this binding motif sets the stage for chemically driven ligand displacement where the binding of amines or alcohols to HfO2 NCs is promoted by the conversion of a bound carboxylic acid into a non-coordinating amide or ester. Furthermore, the sustained ligand displacement, following the addition of excess carboxylic acid, provides a catalytic pathway for ester formation, whereas the addition of esters leads to NC-catalysed transesterification. Because sustained, chemically driven ligand displacement leaves the NCs--including their surface composition--unchanged and preserves colloidal stability, metal oxide nanocrystals are thus turned into effective nanocatalysts that bypass the tradeoff between colloidal stability and catalytic activity.

  11. Recent developments in colloidal synthesis of CuInSe2 nanoparticles.

    PubMed

    Witt, Elena; Kolny-Olesiak, Joanna

    2013-07-22

    Ternary semiconductor nanocrystals, such as CuInSe2 , are of high interest for photovoltaic application due to their relatively low toxicity and unique properties. During the last decades great success has been achieved in the colloidal synthesis of binary nanoparticles, but for ternary compounds this research is still in an early stage of development. These materials are a challenge for synthetic chemistry, because the interaction between the three components (copper, indium, and selenium) plays a major role for the production of high quality material. The purpose of this Minireview is to provide a summary of the achievements in colloidal synthesis of CuInSe2 nanoparticles--in particular, details of reaction mechanism and its characterization possibilities, which might be useful also for the colloidal synthesis of other multicomponent systems. PMID:23788400

  12. Colloidal metal oxide nanocrystal catalysis by sustained chemically driven ligand displacement.

    PubMed

    De Roo, Jonathan; Van Driessche, Isabel; Martins, José C; Hens, Zeger

    2016-05-01

    Surface chemistry is a key enabler for colloidal nanocrystal applications. In this respect, metal oxide nanocrystals (NCs) stand out from other NCs as carboxylic acid ligands adsorb on their surface by dissociation to carboxylates and protons, the latter proving essential in electron transfer reactions. Here, we show that this binding motif sets the stage for chemically driven ligand displacement where the binding of amines or alcohols to HfO2 NCs is promoted by the conversion of a bound carboxylic acid into a non-coordinating amide or ester. Furthermore, the sustained ligand displacement, following the addition of excess carboxylic acid, provides a catalytic pathway for ester formation, whereas the addition of esters leads to NC-catalysed transesterification. Because sustained, chemically driven ligand displacement leaves the NCs-including their surface composition-unchanged and preserves colloidal stability, metal oxide nanocrystals are thus turned into effective nanocatalysts that bypass the tradeoff between colloidal stability and catalytic activity. PMID:26808460

  13. Superconductivity in colloidal lead nanocrystals

    NASA Astrophysics Data System (ADS)

    Zolotavin, Pavlo

    Monodisperse colloidal lead nanoparticles with diameters ranging from 4.4 to 20 nm were prepared by a self-limiting growth method. The nanoparticles are protected from oxidation by an amorphous lead-tin oxide shell of 1.5-2 nm thickness. The magnetic susceptibility of the particles was measured as a function of size, temperature and magnetic field. The Meissner effect was observed indicating the superconducting transition. For the 20 and 16 nm particles, the critical temperature is suppressed to 6.9 K from the bulk value of 7.2 K and is further reduced for smaller particles. Depending on the size of the particles, the critical field is enhanced by 60 to 140 times. The coupling between particles was in situ controlled through the conversion of the oxides present on the surface of the nanoparticles to chalcogenides. This transformation allows for a 109-fold increase in the conductivity. The temperature of the onset of the superconductivity was found to depend upon the degree of coupling of the nanoparticles in the vicinity of the insulator - superconductor transition. The critical current density of the best sample of Pb/PbSe nanocrystals at zero magnetic field was determined to be 4 x 103 A/cm 2. In turn, the critical field of the sample shows 50-fold enhancement compared to bulk Pb. A method to convert the original Pb/PbO nanocrystals into colloidal Pb/PbS (Se, Te) particle was developed. This alleviates the necessity of chemical post processing and provides a truly colloidal superconductor. Paramagnetic Meissner effect of abnormally large amplitude is observed for Pb/PbTe nanocrystal assemblies. The material described in this manuscript is the first nanostructured superconductor prepared by the bottom-up approach starting from colloidal nanoparticles.

  14. Linear viscoelasticity of colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Cichocki, B.; Felderhof, B. U.

    1992-12-01

    We develop a phenomenological theory of the dynamic viscosity of colloidal suspensions, based on an extrapolation of the low-frequency behavior by use of a continued-fraction representation. In lowest approximation the dynamic viscosity depends on a small number of parameters, which may be determined experimentally. For semidilute suspensions the parameters may be found by theoretical calculation. The theory is tested by comparison with an exactly soluble model.

  15. Solid colloidal optical wavelength filter

    NASA Astrophysics Data System (ADS)

    Alvarez, J. L.

    1990-05-01

    A method for constructing a solid colloidal optical wavelength filter is discussed. The device was developed to filter optical wavelengths for spectroscopy, protection from intense radiation, monochromatizing, and analyzing optical radiation. The filter is formed by suspending spherical particles in a coagulable medium (such as setting plastic); agitating the particles and coagulable medium to produce an emulsion of particles suspended in the coagulable medium; and allowing the coagulable medium and suspended emulsion of particles to cool.

  16. Colloidal assembly by ice templating.

    PubMed

    Kumaraswamy, Guruswamy; Biswas, Bipul; Choudhury, Chandan Kumar

    2016-04-12

    We investigate ice templating of aqueous dispersions of polymer coated colloids and crosslinkers, at particle concentrations far below that required to form percolated monoliths. Freezing the aqueous dispersions forces the particles into close proximity to form clusters, that are held together as the polymer chains coating the particles are crosslinked. We observe that, with an increase in the particle concentration from about 10(6) to 10(8) particles per ml, there is a transition from isolated single particles to increasingly larger clusters. In this concentration range, most of the colloidal clusters formed are linear or sheet like particle aggregates. Remarkably, the cluster size distribution for clusters smaller than about 30 particles, as well as the size distribution of linear clusters, is only weakly dependent on the dispersion concentration in the range that we investigate. We demonstrate that the main features of cluster formation are captured by kinetic simulations that do not consider hydrodynamics or instabilities at the growing ice front due to particle concentration gradients. Thus, clustering of colloidal particles by ice templating dilute dispersions appears to be governed only by particle exclusion by the growing ice crystals that leads to their accumulation at ice crystal boundaries. PMID:26780838

  17. Colloidal thermoresponsive gel forming hybrids.

    PubMed

    Liu, Ruixue; Tirelli, Nicola; Cellesi, Francesco; Saunders, Brian R

    2010-09-15

    Colloidal hybrids comprise organic and inorganic components and are attracting considerable attention in the literature. Recently, we reported hybrid anisotropic microsheets that formed thermoresponsive gels in polymer solutions [Liu et al., Langmuir, 25, 490, 2009]. Here, we investigate the composition and properties of these hybrid colloids themselves in detail for the first time. Three different cationic PNIPAm (N-isopropylacrylamide) graft copolymers and two inorganic nanoparticle types (laponite and Ludox silica) were used to prepare a range of hybrids. Anisotropic microsheets only formed when laponite particles were added to the copolymer implying directed self-assembly. Aqueous dispersions of the microsheets spontaneously formed gels at room temperature and these gels were thermoresponsive. They represent a new class of gel forming colloid and are termed thermoresponsive gel forming hybrids. The compositions of the hybrids were determined from thermogravimetric analysis and those that gave gel forming behaviour identified. Variable-temperature rheology experiments showed that the elasticity of the gels increased linearly with temperature. The reversibility of the thermally-triggered changes in gel elasticity was investigated. The concentration dependence of the rheology data was well described by elastic percolation scaling theory and the data could be collapsed onto a master curve. The concentration exponent for the elastic modulus was 2.5. The strong attractive interactions that exist between the dispersed gel forming hybrids was demonstrated by the formation of stable thermoresponsive hybrid hydrogels through casting of hybrid dispersions. PMID:20561633

  18. Crystallization of DNA-coated colloids

    PubMed Central

    Wang, Yu; Wang, Yufeng; Zheng, Xiaolong; Ducrot, Étienne; Yodh, Jeremy S.; Weck, Marcus; Pine, David J.

    2015-01-01

    DNA-coated colloids hold great promise for self-assembly of programmed heterogeneous microstructures, provided they not only bind when cooled below their melting temperature, but also rearrange so that aggregated particles can anneal into the structure that minimizes the free energy. Unfortunately, DNA-coated colloids generally collide and stick forming kinetically arrested random aggregates when the thickness of the DNA coating is much smaller than the particles. Here we report DNA-coated colloids that can rearrange and anneal, thus enabling the growth of large colloidal crystals from a wide range of micrometre-sized DNA-coated colloids for the first time. The kinetics of aggregation, crystallization and defect formation are followed in real time. The crystallization rate exhibits the familiar maximum for intermediate temperature quenches observed in metallic alloys, but over a temperature range smaller by two orders of magnitude, owing to the highly temperature-sensitive diffusion between aggregated DNA-coated colloids. PMID:26078020

  19. Crystallization of DNA-coated colloids.

    PubMed

    Wang, Yu; Wang, Yufeng; Zheng, Xiaolong; Ducrot, Étienne; Yodh, Jeremy S; Weck, Marcus; Pine, David J

    2015-01-01

    DNA-coated colloids hold great promise for self-assembly of programmed heterogeneous microstructures, provided they not only bind when cooled below their melting temperature, but also rearrange so that aggregated particles can anneal into the structure that minimizes the free energy. Unfortunately, DNA-coated colloids generally collide and stick forming kinetically arrested random aggregates when the thickness of the DNA coating is much smaller than the particles. Here we report DNA-coated colloids that can rearrange and anneal, thus enabling the growth of large colloidal crystals from a wide range of micrometre-sized DNA-coated colloids for the first time. The kinetics of aggregation, crystallization and defect formation are followed in real time. The crystallization rate exhibits the familiar maximum for intermediate temperature quenches observed in metallic alloys, but over a temperature range smaller by two orders of magnitude, owing to the highly temperature-sensitive diffusion between aggregated DNA-coated colloids. PMID:26078020

  20. Binodal Colloidal Aggregation Test - 4: Polydispersion

    NASA Technical Reports Server (NTRS)

    Chaikin, Paul M.

    2008-01-01

    Binodal Colloidal Aggregation Test - 4: Polydispersion (BCAT-4-Poly) will use model hard-spheres to explore seeded colloidal crystal nucleation and the effects of polydispersity, providing insight into how nature brings order out of disorder. Crewmembers photograph samples of polymer and colloidal particles (tiny nanoscale spheres suspended in liquid) that model liquid/gas phase changes. Results will help scientists develop fundamental physics concepts previously cloaked by the effects of gravity.

  1. Binary Colloidal Alloy Test Conducted on Mir

    NASA Technical Reports Server (NTRS)

    Hoffmann, Monica I.; Ansari, Rafat R.

    1999-01-01

    Colloids are tiny (submicron) particles suspended in fluid. Paint, ink, and milk are examples of colloids found in everyday life. The Binary Colloidal Alloy Test (BCAT) is part of an extensive series of experiments planned to investigate the fundamental properties of colloids so that scientists can make colloids more useful for technological applications. Some of the colloids studied in BCAT are made of two different sized particles (binary colloidal alloys) that are very tiny, uniform plastic spheres. Under the proper conditions, these colloids can arrange themselves in a pattern to form crystals. These crystals may form the basis of new classes of light switches, displays, and optical devices. Windows made of liquid crystals are already in the marketplace. These windows change their appearance from transparent to opaque when a weak electric current is applied. In the future, if the colloidal crystals can be made to control the passage of light through them, such products could be made much more cheaply. These experiments require the microgravity environment of space because good quality crystals are difficult to produce on Earth because of sedimentation and convection in the fluid. The BCAT experiment hardware included two separate modules for two different experiments. The "Slow Growth" hardware consisted of a 35-mm camera with a 250- exposure photo film cartridge. The camera was aimed toward the sample module, which contained 10 separate colloid samples. A rack of small lights provided backlighting for the photographs. The BCAT hardware was launched on the shuttle and was operated aboard the Russian space station Mir by American astronauts John Blaha and David Wolf (launched September 1996 and returned January 1997; reflown September 1997 and returned January 1998). To begin the experiment, one of these astronauts would mix the samples to disperse the colloidal particles and break up any crystals that might have already formed. Once the samples were mixed and

  2. Circumstellar chemistry

    NASA Technical Reports Server (NTRS)

    Glassgold, Alfred E.; Huggins, Patrick J.

    1987-01-01

    The study of the outer envelopes of cool evolved stars has become an active area of research. The physical properties of CS envelopes are presented. Observations of many wavelengths bands are relevant. A summary of observations and a discussion of theoretical considerations concerning the chemistry are summarized. Recent theoretical considerations show that the thermal equilibrium model is of limited use for understanding the chemistry of the outer CS envelopes. The theoretical modeling of the chemistry of CS envelopes provides a quantitive test of chemical concepts which have a broader interest than the envelopes themselves.

  3. Aggregation kinetics in a model colloidal suspension

    SciTech Connect

    Bastea, S

    2005-08-08

    The authors present molecular dynamics simulations of aggregation kinetics in a colloidal suspension modeled as a highly asymmetric binary mixture. Starting from a configuration with largely uncorrelated colloidal particles the system relaxes by coagulation-fragmentation dynamics to a structured state of low-dimensionality clusters with an exponential size distribution. The results show that short range repulsive interactions alone can give rise to so-called cluster phases. For the present model and probably other, more common colloids, the observed clusters appear to be equilibrium phase fluctuations induced by the entropic inter-colloidal attractions.

  4. Colloid Coalescence with Focused X Rays

    SciTech Connect

    Weon, B. M.; Kim, J. T.; Je, J. H.; Yi, J. M.; Wang, S.; Lee, W.-K.

    2011-07-01

    We show direct evidence that focused x rays enable us to merge polymer colloidal particles at room temperature. This phenomenon is ascribed to the photochemical scission of colloids with x rays, reducing the molecular weight, glass transition temperature, surface tension, and viscosity of colloids. The observation of the neck bridge growth with time shows that the x-ray-induced colloid coalescence is analogous to viscoelastic coalescence. This finding suggests a feasible protocol of photonic nanofabrication by sintering or welding of polymers, without thermal damage, using x-ray photonics.

  5. Conductivity maximum in a charged colloidal suspension

    SciTech Connect

    Bastea, S

    2009-01-27

    Molecular dynamics simulations of a charged colloidal suspension in the salt-free regime show that the system exhibits an electrical conductivity maximum as a function of colloid charge. We attribute this behavior to two main competing effects: colloid effective charge saturation due to counterion 'condensation' and diffusion slowdown due to the relaxation effect. In agreement with previous observations, we also find that the effective transported charge is larger than the one determined by the Stern layer and suggest that it corresponds to the boundary fluid layer at the surface of the colloidal particles.

  6. Collective motion in populations of colloidal bots

    NASA Astrophysics Data System (ADS)

    Bartolo, Denis

    One of the origins of active matter physics was the idea that flocks, herds, swarms and shoals could be quantitatively described as emergent ordered phases in self-driven materials. From a somehow dual perspective, I will show how to engineer active materials our of colloidal flocks. I will show how to motorize colloidal particles capable of sensing the orientation of their neighbors and how to handle them in microfluidic chips. These populations of colloidal bots display a non-equilibrium transition toward collective motion. A special attention will be paid to the robustness of the resulting colloidal flocks with respect to geometrical frustration and to quenched disorder.

  7. Nonequilibrium forces between dragged ultrasoft colloids.

    PubMed

    Singh, Sunil P; Winkler, Roland G; Gompper, Gerhard

    2011-10-01

    The dynamical deformation of ultrasoft colloids as well as their dynamic frictional forces are numerically investigated, when one colloid is dragged past another at constant velocity. Hydrodynamic interactions are captured by a particle-based mesoscopic simulation method. At vanishing relative velocity, the equilibrium repulsive force-distance curve is obtained. At large drag velocities, in contrast, we find an apparent attractive force for departing colloids along the dragging direction. The deformation, in the close encounter of colloids, and the energy dissipation are examined as a function of the drag velocity and their separation. PMID:22107322

  8. Colloid Titration--A Rapid Method for the Determination of Charged Colloid.

    ERIC Educational Resources Information Center

    Ueno, Keihei; Kina, Ken'yu

    1985-01-01

    "Colloid titration" is a volumetric method for determining charged polyelectrolytes in aqueous solutions. The principle of colloid titration, reagents used in the procedure, methods of endpoint detection, preparation of reagent solutions, general procedure used, results obtained, and pH profile of colloid titration are considered. (JN)

  9. SIGNIFICANCE OF STRAINING IN COLLOID DEPOSITION: EVIDENCE AND IMPLICATIONS

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Filtration theory is often used to characterize colloid attachment when deposition is controlled by chemical interactions between colloids and grain surfaces. Over the past decade considerable research suggests that colloid deposition is frequently not consistent with filtration theory predictions u...

  10. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1980

    1980-01-01

    Describes equipment, activities, and experiments useful in chemistry instruction, including among others, a rapid method to determine available chlorine in bleach, simple flame testing apparatus, and a simple apparatus demonstrating the technique of flash photolysis. (SK)

  11. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1973

    1973-01-01

    Several ideas are proposed for chemistry teachers to try in their classrooms. Subjects included are polymerization of acrylate, polymerization of styrene, conductivity, pollution, preparation of chlorine, redox equations, chemiluminescence, and molecular sieves. (PS)

  12. Nuclear Chemistry.

    ERIC Educational Resources Information Center

    Chemical and Engineering News, 1979

    1979-01-01

    Provides a brief review of the latest developments in nuclear chemistry. Nuclear research today is directed toward increased activity in radiopharmaceuticals and formation of new isotopes by high-energy, heavy-ion collisions. (Author/BB)

  13. Catalytic Chemistry.

    ERIC Educational Resources Information Center

    Borer, Londa; And Others

    1996-01-01

    Describes an approach for making chemistry relevant to everyday life. Involves the study of kinetics using the decomposition of hydrogen peroxide by vegetable juices. Allows students to design and carry out experiments and then draw conclusions from their results. (JRH)

  14. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1981

    1981-01-01

    Describes 13 activities, experiments and demonstrations, including the preparation of iron (III) chloride, simple alpha-helix model, investigating camping gas, redox reactions of some organic compounds, a liquid crystal thermometer, and the oxidation number concept in organic chemistry. (JN)

  15. Precolumbian Chemistry.

    ERIC Educational Resources Information Center

    Robinson, Janet Bond

    1995-01-01

    Describes the content and development of a curriculum that provides an approach to descriptive chemistry and the history of technology through consideration of the pottery, metallurgy, pigments, dyes, agriculture, and medicine of pre-Columbian people. (DDR)

  16. Stratospheric chemistry

    SciTech Connect

    Brune, W.H. )

    1991-01-01

    Advances in stratospheric chemistry made by investigators in the United States from 1987 to 1990 are reviewed. Subject areas under consideration include photochemistry of the polar stratosphere, photochemistry of the global stratosphere, and assessments of inadvertent modification of the stratosphere by anthropogenic activity. Particular attention is given to early observations and theories, gas phase chemistry, Antarctic observations, Arctic observations, odd-oxygen, odd-hydrogen, odd-nitrogen, halogens, aerosols, modeling of stratospheric ozone, and reactive nitrogen effects.

  17. Effects of precipitation events on colloids in a karst aquifer

    NASA Astrophysics Data System (ADS)

    Shevenell, Lisa; McCarthy, John F.

    2002-01-01

    The effects of precipitation events on colloid mobilization were evaluated during several storms from six wells in a karstic aquifer at the Oak Ridge Y-12 Plant in eastern Tennessee (USA). Turbidity increases and rapidly recedes following rain events. Although the magnitude of the turbidity increases are relatively small (≤4.78 NTU), the increased turbidity suggests transient increases in colloid abundance during storm versus non-storm periods. During the larger storms (>19 mm), the increased turbidity is associated with increases in pH, total organic carbon (TOC) and temperature, and with decreases in dissolved oxygen (DO). These larger storms result in flushing of a greater proportion of higher pH, TOC (and lower DO) soil or matrix waters into the fractures and conduits than occurs during smaller storms. Smaller storms also result in increases in turbidity, but show increases in DO and decreases in pH reflecting less influence on the water chemistry from the longer residence time epikarst or and matrix waters, and greater impact from the more dilute, newly recharged waters. Due to the complexity of karst flow and temporal variations in flow and chemistry, controls on turbidity are not consistent through time and space at the wells. During smaller storms, recharge by lower ionic strength waters may promote colloid release and thus contribute to observed increases in turbidity. During larger storms, elevated turbidity may be more related to pH increases resulting from greater influx of matrix and soil waters into fractures and conduits. Chemical factors alone cannot account for the changes in turbidity observed during the various storms. Because of the complicated nature of flow and particle transport in karst aquifers, the presence of colloids during precipitation events is dictated by a complex interplay of chemical reactions and the effects of physical perturbations due to increased flow through the conduits and fractures. Simple trends in water quality

  18. Analysis of colloid and tracer breakthrough curves

    NASA Astrophysics Data System (ADS)

    Grindrod, Peter; Edwards, Mark S.; Higgo, Jenny J. W.; Williams, Geoffrey M.

    1996-02-01

    We consider the dispersion and elution of colloids and dissolved nonsorbing tracers within saturated heterogeneous porous media. Since flow path geometry in natural systems is often ill-characterized macroscopic (mean) flow rates and dispersion tensors are utilized in order to account for the sub-model scale microscopic fluctuations in media structure (and the consequent hydrodynamic profile). Even for tracer migration and dispersal this issue is far from settled. Here we consider how colloid and tracer migration phenomena can be treated consistently. Theoretical calculations for model flow geometries yield two quantitative predictions for the transport of free (not yet captured) colloids with reference to a non-sorbing dissolved tracer within the same medium: the average migration velocity of the free colloids is higher than that of the tracer; and that the ratio of the equivalent hydrodynamic dispersion rates of colloids and tracer is dependent only upon properties of the colloids and the porous medium, it is independent of pathlengths and fluid flux, once length scales are large enough. The first of these is well known, since even in simple flow paths free colloids must stay more centre stream. The second, if validated suggests how solute and colloid dispersion may be dealt with consistently in macroscopic migration models. This is crucial since dispersion is usually ill-characterized and unaddressed by the experimental literature. In this paper we present evidence based upon an existing Drigg field injection test for the validity of these predictions. We show that starting from experimental data the fitted dispersion rates of both colloids and non-sorbing tracers increase with the measured elution rates (obeying slightly different rules for tracers and colloids); and that the ratio of colloid and nonsorbing tracer elution rates, and the ratio of colloid and nonsorbing tracer dispersion rates may be dependent upon properties of the colloids and the medium (not

  19. Gold Nanocups: Colloidal Gold Nanocups with Orientation-Dependent Plasmonic Properties (Adv. Mater. 30/2016).

    PubMed

    Jiang, Ruibin; Qin, Feng; Liu, Yejing; Ling, Xing Yi; Guo, Jun; Tang, Minghua; Cheng, Si; Wang, Jianfang

    2016-08-01

    On page 6322, J. F. Wang and co-workers report a wet-chemistry method for the preparation of colloidal Au nanocups and their plasmonic properties. The Au nanocups are prepared through single-vertex-initiated Au deposition on PbS nano-octahedrons and subsequent selective dissolution of PbS. Owing to the orientation-dependent coupling strengths, the obtained Au nanocups display orientation-dependent plasmonic properties and Raman enhancements when deposited on substrates. PMID:27493069

  20. Structural color from colloidal glasses

    NASA Astrophysics Data System (ADS)

    Magkiriadou, Sofia

    When a material has inhomogeneities at a lengthscale comparable to the wavelength of light, interference can give rise to structural colors: colors that originate from the interaction of the material's microstructure with light and do not require absorbing dyes. In this thesis we study a class of these materials, called photonic glasses, where the inhomogeneities form a dense and random arrangement. Photonic glasses have angle-independent structural colors that look like those of conventional dyes. However, when this work started, there was only a handful of colors accessible with photonic glasses, mostly hues of blue. We use various types of colloidal particles to make photonic glasses, and we study, both theoretically and experimentally, how the optical properties of these glasses relate to their structure and constituent particles. Based on our observations from glasses of conventional particles, we construct a theoretical model that explains the scarcity of yellow, orange, and red photonic glasses. Guided by this model, we develop novel colloidal systems that allow a higher degree of control over structural color. We assemble glasses of soft, core-shell particles with scattering cores and transparent shells, where the resonant wavelength can be tuned independently of the reflectivity. We then encapsulate glasses of these core-shell particles into emulsion droplets of tunable size; in this system, we observe, for the first time, angle-independent structural colors that cover the entire visible spectrum. To enhance color saturation, we begin experimenting with inverse glasses, where the refractive index of the particles is lower than the refractive index of the medium, with promising results. Finally, based on our theoretical model for scattering from colloidal glasses, we begin an exploration of the color gamut that could be achieved with this technique, and we find that photonic glasses are a promising approach to a new type of long-lasting, non-toxic, and

  1. Highly uniform polyhedral colloids formed by colloidal crystal templating

    NASA Astrophysics Data System (ADS)

    Wang, Yifan; McGinley, James; Crocker, John; Crocker Research Group Team

    2015-03-01

    We seek to create polyhedral solid particles by trapping oil droplets in a colloidal crystal, and polymerizing them in situ, resulting in polyhedral particles containing spherical dimples in an ordered arrangement. Specifically, highly monodisperse, micron-sized droplets of 3-methacryloxypropyl trimethoxysilane (TPM) were first prepared through a poly condensation reaction, following well established methods. The droplets were mixed with an excess of polystyrene(PS) particles (diameter in 2.58 μm), which formed close packed (FCC or HCP) colloidal crystals by natural sedimentation and compression under partial drying to an extent, with TPM oil droplets trapped into their tetrahedral and octahedral interstitial sites and wet PS particles. Depending on the initial particle volume fraction and extent of drying, a high yield of dimpled particles having different shapes including tetrahedra and cubes were obtained after oil initiated polymerization and dissolution of the host PS particles, as seen under SEM. The effects of TPM to PS particles size ratio, drying time, and other factors in relation to the yield of tetrahedral and cubic dimpled particles will be presented. Finally, fractionation techniques were used to obtain suspensions of uniform polyhedral particles of high purity.

  2. Active colloids at fluid interfaces.

    PubMed

    Malgaretti, P; Popescu, M N; Dietrich, S

    2016-05-01

    If an active Janus particle is trapped at the interface between a liquid and a fluid, its self-propelled motion along the interface is affected by a net torque on the particle due to the viscosity contrast between the two adjacent fluid phases. For a simple model of an active, spherical Janus colloid we analyze the conditions under which translation occurs along the interface and we provide estimates of the corresponding persistence length. We show that under certain conditions the persistence length of such a particle is significantly larger than the corresponding one in the bulk liquid, which is in line with the trends observed in recent experimental studies. PMID:27025167

  3. Colloidal entanglement in highly twisted chiral nematic colloids: twisted loops, Hopf links, and trefoil knots.

    PubMed

    Jampani, V S R; Škarabot, M; Ravnik, M; Čopar, S; Žumer, S; Muševič, I

    2011-09-01

    The topology and geometry of closed defect loops is studied in chiral nematic colloids with variable chirality. The colloidal particles with perpendicular surface anchoring of liquid crystalline molecules are inserted in a twisted nematic cell with the thickness that is only slightly larger than the diameter of the colloidal particle. The total twist of the chiral nematic structure in cells with parallel boundary conditions is set to 0, π, 2π, and 3π, respectively. We use the laser tweezers to discern the number and the topology of the -1/2 defect loops entangling colloidal particles. For a single colloidal particle, we observe that a single defect loop is winding around the particle, with the winding pattern being more complex in cells with higher total twist. We observe that colloidal dimers and colloidal clusters are always entangled by one or several -1/2 defect loops. For colloidal pairs in π-twisted cells, we identify at least 17 different entangled structures, some of them exhibiting linked defect loops-Hopf link. Colloidal entanglement is even richer with a higher number of colloidal particles, where we observe not only linked, but also colloidal clusters knotted into the trefoil knot. The experiments are in good agreement with numerical modeling using Landau-de Gennes theory coupled with geometrical and topological considerations using the method of tetrahedral rotation. PMID:22060386

  4. Colloid transport in dual-permeability media

    Technology Transfer Automated Retrieval System (TEKTRAN)

    It has been widely reported that colloids can travel faster and over longer distances in natural structured porous media than in uniform structureless media used in laboratory studies. The presence of preferential pathways for colloids in the subsurface environment is of concern because of the incre...

  5. Colloidal Electrolytes and the Critical Micelle Concentration

    ERIC Educational Resources Information Center

    Knowlton, L. G.

    1970-01-01

    Describes methods for determining the Critical Micelle Concentration of Colloidal Electrolytes; methods described are: (1) methods based on Colligative Properties, (2) methods based on the Electrical Conductivity of Colloidal Electrolytic Solutions, (3) Dye Method, (4) Dye Solubilization Method, and (5) Surface Tension Method. (BR)

  6. Binary Colloidal Alloy Test-5: Aspheres

    NASA Technical Reports Server (NTRS)

    Chaikin, Paul M.; Hollingsworth, Andrew D.

    2008-01-01

    The Binary Colloidal Alloy Test - 5: Aspheres (BCAT-5-Aspheres) experiment photographs initially randomized colloidal samples (tiny nanoscale spheres suspended in liquid) in microgravity to determine their resulting structure over time. BCAT-5-Aspheres will study the properties of concentrated systems of small particles when they are identical, but not spherical in microgravity..

  7. Radiation Chemistry

    NASA Astrophysics Data System (ADS)

    Wojnárovits, L.

    Ionizing radiation causes chemical changes in the molecules of the interacting medium. The initial molecules change to new molecules, resulting in changes of the physical, chemical, and eventually biological properties of the material. For instance, water decomposes to its elements H2 and O2. In polymers, degradation and crosslinking take place. In biopolymers, e.g., DNS strand breaks and other alterations occur. Such changes are to be avoided in some cases (radiation protection), however, in other cases they are used for technological purposes (radiation processing). This chapter introduces radiation chemistry by discussing the sources of ionizing radiation (radionuclide sources, machine sources), absorption of radiation energy, techniques used in radiation chemistry research, and methods of absorbed energy (absorbed dose) measurements. Radiation chemistry of different classes of inorganic (water and aqueous solutions, inorganic solids, ionic liquids (ILs)) and organic substances (hydrocarbons, halogenated compounds, polymers, and biomolecules) is discussed in concise form together with theoretical and experimental backgrounds. An essential part of the chapter is the introduction of radiation processing technologies in the fields of polymer chemistry, food processing, and sterilization. The application of radiation chemistry to nuclear technology and to protection of environment (flue gas treatment, wastewater treatment) is also discussed.

  8. Stability of Ionic Colloidal Crystals (ICCs)

    NASA Astrophysics Data System (ADS)

    Maskaly, Garry R.; Garcia, R. Edwin; Carter, W. Craig; Chiang, Yet-Ming

    2003-03-01

    Ionic colloidal crystals (ICCs) are here defined as ordered multicomponent colloids formed by attractive electrostatic interactions. Compared to previous approaches to colloidal crystallization, the ICC approach holds the potential for self-assembly of a wide range of structures not easily accessible by other methods. In this work, the colloid-chemical conditions under which ICCs are stable have been theoretically analyzed. A model is presented in which two dimensionless parameters are found to fully characterize an ICC system. We calculate the Madelung constant for ICCs of several classical ionic crystal structures as a function of these two parameters, and discuss the parallels between the ICC Madelung constants and the classical ionic case. Experimentally accessible regions of surface charge, particle sizes, salt concentration, and temperature where ionic colloidal crystallization should be possible are identified.

  9. Shaping Colloids for Self-Assembly

    NASA Astrophysics Data System (ADS)

    Sacanna, Stefano; Yi, Gi-Ra; Pine, David

    2013-03-01

    The creation of a new material often starts from the design of its constituent building blocks at a smaller scale. From macromolecules to colloidal architectures, to granular systems, the interactions between basic units of matter can dictate the macroscopic behavior of the resulting engineered material and even regulate its genesis. Information can be imparted to the building units by altering their physical and chemical properties. In particular, the shape of building blocks plays a fundamental role at the colloidal scale, as it can govern the self-organization of particles into hierarchical structures and ultimately into the desired material. Herein we report a simple and general approach to generate an entire zoo of new anisotropic colloids. Our method is based on a controlled deformation of multiphase colloidal particles that can be selectively liquified, polymerized, dissolved and functionalized in bulk. We further demonstrate control over the particle functionalization and coating by realizing patchy and Janus colloids.

  10. Shaping colloids for self-assembly

    NASA Astrophysics Data System (ADS)

    Sacanna, Stefano; Korpics, Mark; Rodriguez, Kelvin; Colón-Meléndez, Laura; Kim, Seung-Hyun; Pine, David J.; Yi, Gi-Ra

    2013-04-01

    The creation of a new material often starts from the design of its constituent building blocks at a smaller scale. From macromolecules to colloidal architectures, to granular systems, the interactions between basic units of matter can dictate the macroscopic behaviour of the resulting engineered material and even regulate its genesis. Information can be imparted to the building units by altering their physical and chemical properties. In particular, the shape of building blocks has a fundamental role at the colloidal scale, as it can govern the self-organization of particles into hierarchical structures and ultimately into the desired material. Herein we report a simple and general approach to generate an entire zoo of new anisotropic colloids. Our method is based on a controlled deformation of multiphase colloidal particles that can be selectively liquified, polymerized, dissolved and functionalized in bulk. We further demonstrate control over the particle functionalization and coating by realizing patchy and Janus colloids.

  11. Kinetically guided colloidal structure formation

    PubMed Central

    Hecht, Fabian M.; Bausch, Andreas R.

    2016-01-01

    The self-organization of colloidal particles is a promising approach to create novel structures and materials, with applications spanning from smart materials to optoelectronics to quantum computation. However, designing and producing mesoscale-sized structures remains a major challenge because at length scales of 10–100 μm equilibration times already become prohibitively long. Here, we extend the principle of rapid diffusion-limited cluster aggregation (DLCA) to a multicomponent system of spherical colloidal particles to enable the rational design and production of finite-sized anisotropic structures on the mesoscale. In stark contrast to equilibrium self-assembly techniques, kinetic traps are not avoided but exploited to control and guide mesoscopic structure formation. To this end the affinities, size, and stoichiometry of up to five different types of DNA-coated microspheres are adjusted to kinetically control a higher-order hierarchical aggregation process in time. We show that the aggregation process can be fully rationalized by considering an extended analytical DLCA model, allowing us to produce mesoscopic structures of up to 26 µm in diameter. This scale-free approach can easily be extended to any multicomponent system that allows for multiple orthogonal interactions, thus yielding a high potential of facilitating novel materials with tailored plasmonic excitation bands, scattering, biochemical, or mechanical behavior. PMID:27444018

  12. Synthesis of substantially monodispersed colloids

    NASA Technical Reports Server (NTRS)

    Klabunde, Kenneth J. (Inventor); Stoeva, Savka (Inventor); Sorensen, Christopher (Inventor)

    2003-01-01

    A method of forming ligated nanoparticles of the formula Y(Z).sub.x where Y is a nanoparticle selected from the group consisting of elemental metals having atomic numbers ranging from 21-34, 39-52, 57-83 and 89-102, all inclusive, the halides, oxides and sulfides of such metals, and the alkali metal and alkaline earth metal halides, and Z represents ligand moieties such as the alkyl thiols. In the method, a first colloidal dispersion is formed made up of nanoparticles solvated in a molar excess of a first solvent (preferably a ketone such as acetone), a second solvent different than the first solvent (preferably an organic aryl solvent such as toluene) and a quantity of ligand moieties; the first solvent is then removed under vacuum and the ligand moieties ligate to the nanoparticles to give a second colloidal dispersion of the ligated nanoparticles solvated in the second solvent. If substantially monodispersed nanoparticles are desired, the second dispersion is subjected to a digestive ripening process. Upon drying, the ligated nanoparticles may form a three-dimensional superlattice structure.

  13. Nonlinear rheology of colloidal dispersions.

    PubMed

    Brader, J M

    2010-09-15

    Colloidal dispersions are commonly encountered in everyday life and represent an important class of complex fluid. Of particular significance for many commercial products and industrial processes is the ability to control and manipulate the macroscopic flow response of a dispersion by tuning the microscopic interactions between the constituents. An important step towards attaining this goal is the development of robust theoretical methods for predicting from first-principles the rheology and nonequilibrium microstructure of well defined model systems subject to external flow. In this review we give an overview of some promising theoretical approaches and the phenomena they seek to describe, focusing, for simplicity, on systems for which the colloidal particles interact via strongly repulsive, spherically symmetric interactions. In presenting the various theories, we will consider first low volume fraction systems, for which a number of exact results may be derived, before moving on to consider the intermediate and high volume fraction states which present both the most interesting physics and the most demanding technical challenges. In the high volume fraction regime particular emphasis will be given to the rheology of dynamically arrested states. PMID:21386516

  14. Cocklebur-shaped colloidal dispersions.

    PubMed

    Lestage, David J; Urban, Marek W

    2005-11-01

    Unique cocklebur-shaped colloidal dispersions were prepared using a combination of a nanoextruder applied to the aqueous solution containing methyl methacrylate (MMA) and n-butyl acrylate (n-BA) with azo-bis-isobutyronitrile (AIBN) or potassium persulfate (KPS) initiators and stabilized by a mixture of sodium dioctyl sulfosuccinate (SDOSS) and 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (DCPC) phospholipid. Upon extrusion and heating to 75 degrees C, methyl methacrylate/n-butyl acrylate (MMA/nBA) colloidal particles containing tubules pointing outward were obtained as a result of DCPC phospholipids present at the particle surfaces. The same cocklebur-shaped particles were obtained when classical polymerization was used without a nanoextruder under similar compositional and thermal conditions, giving a particle size of 159 nm. However, when Ca(2+) ions are present during polymerization, cocklebur morphologies are disrupted. Because DCPC tubules undergo a transition at 38 degrees C, such cocklebur morphologies may offer numerous opportunities for devices with stimuli-responsive characteristics. PMID:16262269

  15. Colloid-Associated Radionuclide Concentration Limits: ANL

    SciTech Connect

    C. Mertz

    2000-12-21

    The purpose and scope of this report is to describe the analysis of available colloidal data from waste form corrosion tests at Argonne National Laboratory (ANL) to extract characteristics of these colloids that can be used in modeling their contribution to the source term for sparingly soluble radioelements (e.g., Pu). Specifically, the focus is on developing a useful description of the following waste form colloid characteristics: (1) composition, (2) size distribution, and (3) quantification of the rate of waste form colloid generation. The composition and size distribution information are intended to support analysis of the potential transport of the sparingly soluble radionuclides associated with the waste form colloids. The rate of colloid generation is intended to support analysis of the waste form colloid-associated radionuclide concentrations. In addressing the above characteristics, available data are interpreted to address mechanisms controlling colloid formation and stability. This report was developed in accordance with the ''Technical Work Plan for Waste Form Degradation Process Model Report for SR'' (CRWMS M&O 2000). Because the end objective is to support the source term modeling we have organized the conclusions into two categories: (1) data analysis conclusions and (2) recommendations for colloid source term modeling. The second category is included to facilitate use of the conclusions from the data analysis in the abstraction of a colloid source term model. The data analyses and conclusions that are presented in this report are based on small-scale laboratory tests conducted on a limited number of waste glass compositions and spent fuel types.

  16. Chemistry Experiments

    NASA Technical Reports Server (NTRS)

    Brasseur, Guy; Remsberg, Ellis; Purcell, Patrick; Bhatt, Praful; Sage, Karen H.; Brown, Donald E.; Scott, Courtney J.; Ko, Malcolm K. W.; Tie, Xue-Xi; Huang, Theresa

    1999-01-01

    The purpose of the chemistry component of the model comparison is to assess to what extent differences in the formulation of chemical processes explain the variance between model results. Observed concentrations of chemical compounds are used to estimate to what degree the various models represent realistic situations. For readability, the materials for the chemistry experiment are reported in three separate sections. This section discussed the data used to evaluate the models in their simulation of the source gases and the Nitrogen compounds (NO(y)) and Chlorine compounds (Cl(y)) species.

  17. Tropospheric chemistry

    NASA Technical Reports Server (NTRS)

    Mohnen, V. A.; Chameides, W.; Demerjian, K. L.; Lenschow, D. H.; Logan, J. A.; Mcneal, R. J.; Penkett, S. A.; Platt, U.; Schurath, U.; Dias, P. D.

    1985-01-01

    The chemistry of the background troposphere, the source region, and the transition regions are discussed. The troposphere is governed by heterogeneous chemistry far more so than the stratosphere. Heterogeneous processes of interest involve scavenging of trace gases by aerosols, cloud and precipitation elements leading to aqueous phase chemical reactions and to temporary and permanent removal of material from the gas phase. Dry deposition is a major removal process for ozone, as well as for other gases of importance in tropospheric photochemistry. These processes are also discussed.

  18. Polymer Chemistry

    NASA Technical Reports Server (NTRS)

    Williams, Martha; Roberson, Luke; Caraccio, Anne

    2010-01-01

    This viewgraph presentation describes new technologies in polymer and material chemistry that benefits NASA programs and missions. The topics include: 1) What are Polymers?; 2) History of Polymer Chemistry; 3) Composites/Materials Development at KSC; 4) Why Wiring; 5) Next Generation Wiring Materials; 6) Wire System Materials and Integration; 7) Self-Healing Wire Repair; 8) Smart Wiring Summary; 9) Fire and Polymers; 10) Aerogel Technology; 11) Aerogel Composites; 12) Aerogels for Oil Remediation; 13) KSC's Solution; 14) Chemochromic Hydrogen Sensors; 15) STS-130 and 131 Operations; 16) HyperPigment; 17) Antimicrobial Materials; 18) Conductive Inks Formulations for Multiple Applications; and 19) Testing and Processing Equipment.

  19. In-Package Chemistry Abstraction

    SciTech Connect

    E. Thomas

    2004-11-09

    breached but the drip shield remains intact, so all of the seepage flow is diverted from the waste package. The chemistry from the vapor influx case is used to determine the stability of colloids and the solubility of radionuclides available for transport by diffusion, and to determine the degradation rates for the waste forms. TSPA-LA uses the water influx case for the seismic scenario, where the waste package has been breached and the drip shield has been damaged such that seepage flow is actually directed into the waste package. The chemistry from the water influx case that is a function of the flow rate is used to determine the stability of colloids and the solubility of radionuclides available for transport by diffusion and advection, and to determine the degradation rates for the CSNF and HLW glass. TSPA-LA does not use this model for the igneous scenario. Outputs from the in-package chemistry model implemented inside TSPA-LA include pH, ionic strength, and total carbonate concentration. These inputs to TSPA-LA will be linked to the following principle factors: dissolution rates of the CSNF and HLWG, dissolved concentrations of radionuclides, and colloid generation.

  20. Preclinical evaluation of tacrolimus colloidal dispersion for inhalation.

    PubMed

    Watts, Alan B; Peters, Jay I; Talbert, Robert L; O'Donnell, Kevin P; Coalson, Jacqueline J; Williams, Robert O

    2011-02-01

    Substantial improvements in transplant therapy have been made in the past four decades resulting in the acceptance of organ transplantation as a viable treatment for late-stage disease and organ failure. More recently, lung transplantation has gained acceptance; however, high incidence of chronic rejection and opportunistic infections has limited success rates in comparison with other transplant procedures. To achieve more targeted therapy, pulmonary administration of nebulized tacrolimus (TAC) colloidal dispersion once daily for 28 consecutive days in Sprague Dawley (SD) rats has been investigated for safety and systemic elimination. A liquid dispersion of colloidal TAC and lactose (1:1 ratio by weight) was aerosolized using a vibrating mesh nebulizer and administered via a nose-only dosing chamber. Blood chemistry and histological comparisons to saline-dosed animals showed no clinically significant differences in liver and kidney function or lung tissue damage. Maximum blood and lung concentrations sampled 1h after the final dose showed TAC concentrations of 10.1 ± 1.4 ng/mL and 1758.7 ± 80.0 ng/g, respectively. Twenty-four hours after the final dose, systemic TAC concentrations measured 1.0 ± 0.5 ng/mL, which is well below clinically accepted trough concentrations (5-15 ng/mL) for maintenance therapy, and therefore, would not be expected to induce toxic side effects. The propensity for pulmonary retention seen when compared to single dose lung levels may be due to macrophage uptake and the lipophilic nature of TAC. Additionally, three month stability testing of TAC powder for reconstitution showed no changes in amorphous nature or drug potency when stored at ambient conditions. TAC colloidal dispersion proved to be non-toxic when administered by pulmonary inhalation to SD rats over 28 days while providing therapeutic concentrations locally. This delivery strategy may prove safe and effective for the prevention of lung allograft rejection in lung transplant

  1. Programmable colloidal molecules from sequential capillarity-assisted particle assembly

    PubMed Central

    Ni, Songbo; Leemann, Jessica; Buttinoni, Ivo; Isa, Lucio; Wolf, Heiko

    2016-01-01

    The assembly of artificial nanostructured and microstructured materials which display structures and functionalities that mimic nature’s complexity requires building blocks with specific and directional interactions, analogous to those displayed at the molecular level. Despite remarkable progress in synthesizing “patchy” particles encoding anisotropic interactions, most current methods are restricted to integrating up to two compositional patches on a single “molecule” and to objects with simple shapes. Currently, decoupling functionality and shape to achieve full compositional and geometrical programmability remains an elusive task. We use sequential capillarity-assisted particle assembly which uniquely fulfills the demands described above. This is a new method based on simple, yet essential, adaptations to the well-known capillary assembly of particles over topographical templates. Tuning the depth of the assembly sites (traps) and the surface tension of moving droplets of colloidal suspensions enables controlled stepwise filling of traps to “synthesize” colloidal molecules. After deposition and mechanical linkage, the colloidal molecules can be dispersed in a solvent. The template’s shape solely controls the molecule’s geometry, whereas the filling sequence independently determines its composition. No specific surface chemistry is required, and multifunctional molecules with organic and inorganic moieties can be fabricated. We demonstrate the “synthesis” of a library of structures, ranging from dumbbells and triangles to units resembling bar codes, block copolymers, surfactants, and three-dimensional chiral objects. The full programmability of our approach opens up new directions not only for assembling and studying complex materials with single-particle-level control but also for fabricating new microscale devices for sensing, patterning, and delivery applications. PMID:27051882

  2. Programmable colloidal molecules from sequential capillarity-assisted particle assembly.

    PubMed

    Ni, Songbo; Leemann, Jessica; Buttinoni, Ivo; Isa, Lucio; Wolf, Heiko

    2016-04-01

    The assembly of artificial nanostructured and microstructured materials which display structures and functionalities that mimic nature's complexity requires building blocks with specific and directional interactions, analogous to those displayed at the molecular level. Despite remarkable progress in synthesizing "patchy" particles encoding anisotropic interactions, most current methods are restricted to integrating up to two compositional patches on a single "molecule" and to objects with simple shapes. Currently, decoupling functionality and shape to achieve full compositional and geometrical programmability remains an elusive task. We use sequential capillarity-assisted particle assembly which uniquely fulfills the demands described above. This is a new method based on simple, yet essential, adaptations to the well-known capillary assembly of particles over topographical templates. Tuning the depth of the assembly sites (traps) and the surface tension of moving droplets of colloidal suspensions enables controlled stepwise filling of traps to "synthesize" colloidal molecules. After deposition and mechanical linkage, the colloidal molecules can be dispersed in a solvent. The template's shape solely controls the molecule's geometry, whereas the filling sequence independently determines its composition. No specific surface chemistry is required, and multifunctional molecules with organic and inorganic moieties can be fabricated. We demonstrate the "synthesis" of a library of structures, ranging from dumbbells and triangles to units resembling bar codes, block copolymers, surfactants, and three-dimensional chiral objects. The full programmability of our approach opens up new directions not only for assembling and studying complex materials with single-particle-level control but also for fabricating new microscale devices for sensing, patterning, and delivery applications. PMID:27051882

  3. Controlling colloid charge in nonpolar liquids with surfactants.

    PubMed

    Smith, Gregory N; Eastoe, Julian

    2013-01-14

    The formation of ions in nonpolar solvents (with relative permittivity ε(r) of approximately 2) is more difficult than in polar liquids; however, these charged species play an important role in many applications, such as electrophoretic displays. The low relative permittivities of these solvents mean that charges have to be separated by large distances to be stable (approximately 28 nm or 40 times that in water). The inverse micelles formed by surfactants in these solvents provide an environment to stabilize ions and charges. Common surfactants used are sodium dioctylsulfosuccinate (Aerosol OT or AOT), polyisobutylene succinimide, sorbitan oleate, and zirconyl 2-ethyl hexanoate. The behavior of charged inverse micelles has been studied on both the bulk and on the microscopic scale and can be used to determine the motion of the micelles, their structure, and the nature of the electrostatic double layer. Colloidal particles are only weakly charged in the absence of surfactant, but in the presence of surfactants, many types, including polymers, metal oxides, carbon blacks, and pigments, have been observed to become positively or negatively charged. Several mechanisms have been proposed as the origin of surface charge, including acid-base reactions between the colloid and the inverse micelle, preferential adsorption of charged inverse micelles, or dissolution of surface species. While most studies vary only the concentration of surfactant, systematic variation of the particle surface chemistry or the surfactant structure have provided insight into the origin of charging in nonpolar liquids. By carefully varying system parameters and working to understand the interactions between surfactants and colloidal surfaces, further advances will be made leading to better understanding of the origin of charge and to the development of more effective surfactants. PMID:23187453

  4. Plutonium and Cesium Colloid Mediated Transport

    NASA Astrophysics Data System (ADS)

    Boukhalfa, H.; Dittrich, T.; Reimus, P. W.; Ware, D.; Erdmann, B.; Wasserman, N. L.; Abdel-Fattah, A. I.

    2013-12-01

    Plutonium and cesium have been released to the environment at many different locations worldwide and are present in spent fuel at significant levels. Accurate understanding of the mechanisms that control their fate and transport in the environment is important for the management of contaminated sites, for forensic applications, and for the development of robust repositories for the disposal of spent nuclear fuel and nuclear waste. Plutonium, which can be present in the environment in multiple oxidations states and various chemical forms including amorphous oxy(hydr)oxide phases, adsorbs/adheres very strongly to geological materials and is usually immobile in all its chemical forms. However, when associated with natural colloids, it has the potential to migrate significant distances from its point of release. Like plutonium, cesium is not very mobile and tends to remain adhered to geological materials near its release point, although its transport can be enhanced by natural colloids. However, the reactivity of plutonium and cesium are very different, so their colloid-mediated transport might be significantly different in subsurface environments. In this study, we performed controlled experiments in two identically-prepared columns; one dedicated to Pu and natural colloid transport experiments, and the other to Cs and colloid experiments. Multiple flow-through experiments were conducted in each column, with the effluent solutions being collected and re-injected into the same column two times to examine the persistence and scaling behavior of the natural colloids, Pu and Cs. The data show that that a significant fraction of colloids were retained in the first elution through each column, but the eluted colloids collected from the first run transported almost conservatively in subsequent runs. Plutonium transport tracked natural colloids in the first run but deviated from the transport of natural colloids in the second and third runs. Cesium transport tracked natural

  5. Multidentate block-copolymer-stabilized ultrasmall superparamagnetic iron oxide nanoparticles with enhanced colloidal stability for magnetic resonance imaging.

    PubMed

    Chan, Nicky; Laprise-Pelletier, Myriam; Chevallier, Pascale; Bianchi, Andrea; Fortin, Marc-André; Oh, Jung Kwon

    2014-06-01

    Ultrasmall superparamagnetic iron oxide nanoparticles (USPIOs) with diameters <5 nm hold great promise as T1-positive contrast agents for in vivo magnetic resonance imaging. However, control of the surface chemistry of USPIOs to ensure individual colloidal USPIOs with a ligand monolayer and to impart biocompatibility and enhanced colloidal stability is essential for successful clinical applications. Herein, an effective and versatile strategy enabling the development of aqueous colloidal USPIOs stabilized with well-defined multidentate block copolymers (MDBCs) is reported. The multifunctional MDBCs are designed to consist of an anchoring block possessing pendant carboxylates as multidentate anchoring groups strongly bound to USPIO surfaces and a hydrophilic block having pendant hydrophilic oligo(ethylene oxide) chains to confer water dispersibility and biocompatibility. The surface of USPIOs is saturated with multiple anchoring groups of MDBCs, thus exhibiting excellent long-term colloidal stability as well as enhanced colloidal stability at biologically relevant electrolyte, pH, and temperature conditions. Furthermore, relaxometric properties as well as in vitro and in vivo MR imaging results demonstrate that the MDBC-stabilized USPIO colloids hold great potential as an effective T1 contrast agent. PMID:24785001

  6. Colloid Transport in Saturated Porous Media: Elimination of Attachment Efficiency in a New Colloid Transport Model

    SciTech Connect

    Landkamer, Lee L.; Harvey, Ronald W.; Scheibe, Timothy D.; Ryan, Joseph N.

    2013-05-11

    A new colloid transport model is introduced that is conceptually simple but captures the essential features of complicated attachment and detachment behavior of colloids when conditions of secondary minimum attachment exist. This model eliminates the empirical concept of collision efficiency; the attachment rate is computed directly from colloid filtration theory. Also, a new paradigm for colloid detachment based on colloid population heterogeneity is introduced. Assuming the dispersion coefficient can be estimated from tracer behavior, this model has only two fitting parameters: (1) the fraction of colloids that attach irreversibly and (2) the rate at which reversibly attached colloids leave the surface. These two parameters were correlated to physical parameters that control colloid transport such as the depth of the secondary minimum and pore water velocity. Given this correlation, the model serves as a heuristic tool for exploring the influence of physical parameters such as surface potential and fluid velocity on colloid transport. This model can be extended to heterogeneous systems characterized by both primary and secondary minimum deposition by simply increasing the fraction of colloids that attach irreversibly.

  7. Polymer-Induced Depletion Interaction and Its Effect on Colloidal Sedimentation in Colloid-Polymer Mixtures

    NASA Technical Reports Server (NTRS)

    Tong, Penger

    1996-01-01

    In this paper we focus on the polymer-induced depletion attraction and its effect on colloidal sedimentation in colloid-polymer mixtures. We first report a small angle neutron scattering (SANS) study of the depletion effect in a mixture of hard-sphere-like colloid and non-adsorbing polymer. Then we present results of our recent sedimentation measurements in the same colloid-polymer mixture. A key parameter in controlling the sedimentation of heavy colloidal particles is the interparticle potential U(tau), which is the work required to bring two colloidal particles from infinity to a distance tau under a give solvent condition. This potential is known to affect the average settling velocity of the particles and experimentally one needs to have a way to continuously vary U(tau) in order to test the theory. The interaction potential U(tau) can be altered by adding polymer molecules into the colloidal suspension. In a mixture of colloid and non-adsorbing polymer, the potential U(tau) can develop an attractive well because of the depletion effect, in that the polymer chains are expelled from the region between two colloidal particles when their surface separation becomes smaller than the size of the polymer chains. The exclusion of polymer molecules from the space between the colloidal particles leads to an unbalanced osmotic pressure difference pushing the colloidal particles together, which results in an effective attraction between the two colloidal particles. The polymer-induced depletion attraction controls the phase stability of many colloid-polymer mixtures, which are directly of interest to industry.

  8. Engineering novel mesoscopic structures using DNA-programmed colloidal self-assembly

    NASA Astrophysics Data System (ADS)

    Kim, Anthony Ji

    Controlling interactions between colloidal suspensions has been a fascinating challenge both experimentally and theoretically. Three-dimensional colloidal crystals assembled from monodisperse colloidal particles have generated a significant interest because of their potential application as photonic band gap materials (PBG), chemical sensors, optical filters, and switches. DNA-mediated colloidal assembly offers a unique tool for controlling the range and magnitude of interparticle interaction to promote novel crystal formation. We try to delimit those conditions under which the DNA-mediated interaction gives rise to well-ordered 3-D colloidal crystals, as well as to discuss the applications, optimization, and ultimate limitations of such DNA-mediated particle self-assembly. There are many unknowns regarding the expected colloidal phase diagram and the strength and kinetics of the DNA-mediated interaction, as well as the nonspecific interactions between colloids with different surface chemistries. We start with the simplest case of one-component system, where every colloid has a DNA-mediated attraction to every other, since the phase behavior and kinetics of one-component dispersions is well understood from previous studies. We determine and model the temperature and DNA-density dependence of the self-assembly phase diagram and kinetics. We find that crystals only form with the sterically stabilized DNA-particles in a rather narrow range of temperatures and have acceptably fast nucleation and growth in a small range of grafted-DNA density. In addition, the phase behavior of binary alloy solid solutions is studied using the same sterically stabilized colloidal particles. A competition between DNA single-base mismatches is used to create energy penalties for the substitution of a few KBTs'. The minority species substitute into the crystal lattice when the pair interaction difference is a fraction of a K BT, however, they exclude from the growing crystal when the pair

  9. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1972

    1972-01-01

    Short articles on the kinetics of the hydrogen peroxide-iodide ion reaction, simulation of fluidization catalysis, the use of Newman projection diagrams to represent steric relationships in organic chemistry, the use of synthetic substrates for proteolytic enzyme reactions, and two simple clock reactions"--hydrolysis of halogenoalkanes and…

  10. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1983

    1983-01-01

    Presents chemistry experiments, laboratory procedures, demonstrations, teaching suggestions, and classroom materials/activities. These include: game for teaching ionic formulas; method for balancing equations; description of useful redox series; computer programs (with listings) for water electrolysis simulation and for determining chemical…

  11. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1978

    1978-01-01

    Describes some laboratory apparatus, chemistry experiments and demonstrations, such as a Kofler block melting point apparatus, chromatographic investigation of the phosphoric acid, x-ray diffraction, the fountain experiment, endothermic sherbet, the measurement of viscosity, ionization energies and electronic configurations. (GA)

  12. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1982

    1982-01-01

    Presents procedures, experiments, demonstrations, teaching suggestions, and information on a variety of chemistry topics including, for example, inert gases, light-induced reactions, calculators, identification of substituted acetophenones, the elements, analysis of copper minerals, extraction of metallic strontium, equilibrium, halogens, and…

  13. Chemistry Notes.

    ERIC Educational Resources Information Center

    School Science Review, 1980

    1980-01-01

    Presents 12 chemistry notes for British secondary school teachers. Some of these notes are: (1) a simple device for testing pH-meters; (2) portable fume cupboard safety screen; and (3) Mass spectroscopy-analysis of a mass peak. (HM)

  14. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1976

    1976-01-01

    Describes several chemistry projects, including solubility, formula for magnesium oxide, dissociation of dinitrogen tetroxide, use of 1-chloro-2, 4-dinitrobenzene, migration of ions, heats of neutralizations, use of pocket calculators, sonic cleaning, oxidation states of manganese, and cell potentials. Includes an extract from Chemical Age on…

  15. Chemistry Notes

    ERIC Educational Resources Information Center

    School Science Review, 1972

    1972-01-01

    Short articles on the alkylation of aniline, the preparation and properties of perbromate, using scrap copper in chemistry instruction, a safe method of burning hydrogen, and the use of an ion-charge model as an alternative to the mole concept in secondary school instruction. (AL)

  16. Structural evolution of Colloidal Gels under Flow

    NASA Astrophysics Data System (ADS)

    Boromand, Arman; Maia, Joao; Jamali, Safa

    Colloidal suspensions are ubiquitous in different industrial applications ranging from cosmetic and food industries to soft robotics and aerospace. Owing to the fact that mechanical properties of colloidal gels are controlled by its microstructure and network topology, we trace the particles in the networks formed under different attraction potentials and try to find a universal behavior in yielding of colloidal gels. Many authors have implemented different simulation techniques such as molecular dynamics (MD) and Brownian dynamics (BD) to capture better picture during phase separation and yielding mechanism in colloidal system with short-ranged attractive force. However, BD neglects multi-body hydrodynamic interactions (HI) which are believed to be responsible for the second yielding of colloidal gels. We envision using dissipative particle dynamics (DPD) with modified depletion potential and hydrodynamic interactions, as a coarse-grain model, can provide a robust simulation package to address the gel formation process and yielding in short ranged-attractive colloidal systems. The behavior of colloidal gels with different attraction potentials under flow is examined and structural fingerprints of yielding in these systems will be discussed.

  17. Quantification of hydrophobic interaction affinity of colloids

    NASA Astrophysics Data System (ADS)

    Saini, G.; Nasholm, N.; Wood, B. D.

    2009-12-01

    Colloids play an important role in a wide variety of disciplines, including water and wastewater treatment, subsurface transport of metals and organic contaminants, migration of fines in oil reservoirs, biocolloid (virus and bacteria) transport in subsurface, and are integral to laboratory transport studies. Although the role of hydrophobicity in adhesion and transport of colloids, particularly bacteria, is well known; there is scarcity of literature regarding hydrophobicity measurement of non-bacterial colloids and other micron-sized particles. Here we detail an experimental approach based on differential partitioning of colloids between two liquid phases (hydrocarbon and buffer) as a measure of the hydrophobic interaction affinity of colloids. This assay, known as Microbial adhesion to hydrocarbons or MATH, is frequently used in microbiology and bacteriology for quantifying the hydrophobicity of microbes. Monodispersed colloids and particles, with sizes ranging from 1 micron to 33 micron, were used for the experiments. A range of hydrophobicity values were observed for different particles. The hydrophobicity results are also verified against water contact angle measurements of these particles. This liquid-liquid partitioning assay is quick, easy-to-perform and requires minimal instrumentation. Estimation of the hydrophobic interaction affinity of colloids would lead to a better understanding of their adhesion to different surfaces and subsequent transport in porous media.

  18. Dendronized iron oxide colloids for imaging the sentinel lymph node

    NASA Astrophysics Data System (ADS)

    Jouhannaud, J.; Garofalo, A.; Felder-Flesch, D.; Pourroy, G.

    2015-03-01

    Various methods have been used in medicine for more than one century to explore the lymphatic system. Radioactive colloids (RuS labelled with 99mTc) or/and Vital Blue dye are injected around the primary tumour and detected by means of nuclear probe or visual colour inspection respectively. The simultaneous clinical use of both markers (dye and radionuclide) improves the sensitivity of detection close to 100%. Superparamagnetic iron oxides (SPIOs) are currently receiving much attention as strong T2 weighted magnetic resonance imaging contrast agents that can be potentially used for preoperative localization of sentinel nodes, but also for peroperative detection of sentinel node using hand-held probes. In that context, we present the elaboration of dendronized iron oxide nanoparticles elaborated at the Institute of Physics and Chemistry of Materials of Strasbourg.

  19. Colloidal quantum dots for low-cost MWIR imaging

    NASA Astrophysics Data System (ADS)

    Ciani, Anthony J.; Pimpinella, Richard E.; Grein, Christoph H.; Guyot-Sionnest, Philippe

    2016-05-01

    Monodisperse suspensions of HgTe colloidal quantum dots (CQD) are readily synthesized with infrared energy gaps between 3 and 12 microns. Infrared photodetection using dried films of these CQDs has been demonstrated up to a wavelength of 12 microns, and HgTe CQD single-elemnet devices with 3.6 micron cutoff have bee nreported nad show ogod absorption <(10^4 cm^-1), response time and detectivity (2*10^10 Jones) at at emperature of 175 K; with the potential fo uncooled imaging. The synthesis of CQDs and fabrication of detector devices employ bench-top chemistry techniques, leading to the potential for rapid, wafer-scale manufacture of MWIR imaging devices with low production costs and overhead. The photoconductive, photovoltaic and optical properties of HgTe CQD films will be discussed relative to infrared imaging, along with recent achievements in integrating CQD films with readout integrated circuits to produce CQD-based MWIR focal plane arrays.

  20. Interactions between radioactively labeled colloids and natural particles: Evidence for colloidal pumping

    NASA Astrophysics Data System (ADS)

    Wen, Liang-Saw; Santschi, Peter H.; Tang, Degui

    1997-07-01

    It has been hypothesized that colloidal forms of trace metals can be reactive intermediaries in the scavenging processes leading to the removal of their particulate forms. A series of radiotracer experiments using natural colloidal organic matter from Galveston Bay, USA were carried out in order to test this hypothesis. Suspended particle uptake of originally colloidally bound trace metals occurred in a matter of hours to days in estuarine waters. After ten days, the majority (>50%) of the colloidal trace metals had been transferred into the particulate phase (≥0.45 μm), except for 65Zn. Two distinctively different temporal regions of removal of colloidal trace metals were identified: a faster reaction during the first four hours, followed by a slower reaction after approximately one day. In a separate river water-seawater mixing experiment, the solid/solution partitioning of the radiotracers was investigated in the absence of suspended matter. About 30% of most of the elements, except Ag and Fe (˜60%), were associated with a newly formed particulate phase after eight days. There were two major trends: (1) the particulate fraction of 59Fe and 110Ag increased while the colloidal fraction decreased, suggesting a colloidal pumping mechanism. (2) The particulate fraction of 54Mn, 133Ba, 65Zn, 109Cd, 113Sn, and 60CO increased while the LMW (≤ 1 kDa) fraction decreased, suggesting a direct uptake into the particulate fraction with less involvement of a transitory colloidal phase. The values of the particle-water ( Kd) and colloid-water partitioning ( Kc) coefficients for most trace metals were similar to those observed in Galveston Bay waters, suggesting complementary results to field studies. The results from these experiments suggested two different pathways for colloidal tracer uptake by particles: (1) colloidal pumping of a major component (e.g., biopolymer) of the colloidal pool and (2) coagulation of trace components (e.g., phytochelatins) with varying

  1. Assembly of open clusters of colloidal dumbbells via droplet evaporation

    NASA Astrophysics Data System (ADS)

    Pham Van, Hai; Fortini, Andrea; Schmidt, Matthias

    2016-05-01

    We investigate the behavior of a mixture of asymmetric colloidal dumbbells and emulsion droplets by means of kinetic Monte Carlo simulations. The evaporation of the droplets and the competition between droplet-colloid attraction and colloid-colloid interactions lead to the formation of clusters built up of colloid aggregates with both closed and open structures. We find that stable packings and hence complex colloidal structures can be obtained by changing the relative size of the colloidal spheres and/or their interfacial tension with the droplets.

  2. Colloids at NAPL-Interfaces

    NASA Astrophysics Data System (ADS)

    Baumann, Thomas; Metz, Christian

    2014-05-01

    Non-aqueous phase liquids in subsurface are relevant in the scope of contaminated sites as well as for enhanced oil recovery. In both cases colloids and engineered nanoparticles are applied to increase the efficiency of NAPL removal. Particle tracking experiments using fluoresecent latex beads and opaque particles have been run in micromodels mimicking the pore structure of subsurface media. The results show that the interface between NAPL and water is highly dynamic, especially in its early stage. There is a distinct circular flow pattern at the interface, effectively increasing the interfacial area. Concentration gradients measured with Raman Microspectrometry at low Peclet numbers suggest that the mass transfer of dissolved contaminants from the NAPL into the water is highly affected by the interface dynamics. On the other hand the interfaces themselves are less accessible, which has implications for the remediation of contaminated sites.

  3. Colloidal QDs-polymer nanocomposites

    NASA Astrophysics Data System (ADS)

    Gordillo, H.; Suárez, I.; Rodríguez-Cantó, P.; Abargues, R.; García-Calzada, R.; Chyrvony, V.; Albert, S.; Martínez-Pastor, J.

    2012-04-01

    Nanometer-size colloidal semiconductor nanocrystals, or Quantum Dots (NQD), are very prospective active centers because their light emission is highly efficient and temperature-independent. Nanocomposites based on the incorporation of QDs inside a polymer matrix are very promising materials for application in future photonic devices because they combine the properties of QDs with the technological feasibility of polymers. In the present work some basic applications of these new materials have been studied. Firstly, the fabrication of planar and linear waveguides based on the incorporation of CdS, CdSe and CdTe in PMMA and SU-8 are demonstrated. As a result, photoluminescence (PL) of the QDs are coupled to a waveguide mode, being it able to obtain multicolor waveguiding. Secondly, nanocomposite films have been evaluated as photon energy down-shifting converters to improve the efficiency of solar cells.

  4. Three-dimensional ultrasonic colloidal crystals

    NASA Astrophysics Data System (ADS)

    Caleap, Mihai; Drinkwater, Bruce W.

    2016-05-01

    Colloidal assembly represents a powerful method for the fabrication of functional materials. In this article, we describe how acoustic radiation forces can guide the assembly of colloidal particles into structures that serve as microscopic elements in novel acoustic metadevices or act as phononic crystals. Using a simple three-dimensional orthogonal system, we show that a diversity of colloidal structures with orthorhombic symmetry can be assembled with megahertz-frequency (MHz) standing pressure waves. These structures allow rapid tuning of acoustic properties and provide a new platform for dynamic metamaterial applications. xml:lang="fr"

  5. Transport in charged colloids driven by thermoelectricity.

    PubMed

    Würger, Alois

    2008-09-01

    We study the thermal diffusion coefficient D{T} of a charged colloid in a temperature gradient, and find that it is to a large extent determined by the thermoelectric response of the electrolyte solution. The thermally induced salinity gradient leads in general to a strong increase with temperature. The difference of the heat of transport of coions and counterions gives rise to a thermoelectric field that drives the colloid to the cold or to the warm, depending on the sign of its charge. Our results provide an explanation for recent experimental findings on thermophoresis in colloidal suspensions. PMID:18851262

  6. A colloidal quantum dot spectrometer

    NASA Astrophysics Data System (ADS)

    Bao, Jie; Bawendi, Moungi G.

    2015-07-01

    Spectroscopy is carried out in almost every field of science, whenever light interacts with matter. Although sophisticated instruments with impressive performance characteristics are available, much effort continues to be invested in the development of miniaturized, cheap and easy-to-use systems. Current microspectrometer designs mostly use interference filters and interferometric optics that limit their photon efficiency, resolution and spectral range. Here we show that many of these limitations can be overcome by replacing interferometric optics with a two-dimensional absorptive filter array composed of colloidal quantum dots. Instead of measuring different bands of a spectrum individually after introducing temporal or spatial separations with gratings or interference-based narrowband filters, a colloidal quantum dot spectrometer measures a light spectrum based on the wavelength multiplexing principle: multiple spectral bands are encoded and detected simultaneously with one filter and one detector, respectively, with the array format allowing the process to be efficiently repeated many times using different filters with different encoding so that sufficient information is obtained to enable computational reconstruction of the target spectrum. We illustrate the performance of such a quantum dot microspectrometer, made from 195 different types of quantum dots with absorption features that cover a spectral range of 300 nanometres, by measuring shifts in spectral peak positions as small as one nanometre. Given this performance, demonstrable avenues for further improvement, the ease with which quantum dots can be processed and integrated, and their numerous finely tuneable bandgaps that cover a broad spectral range, we expect that quantum dot microspectrometers will be useful in applications where minimizing size, weight, cost and complexity of the spectrometer are critical.

  7. Colloid-Facilitated Transport of Radionuclides through the Vadose Zone

    SciTech Connect

    Flury, Markus; Harsh, James B.; Zachara, John M.; McCarthy, John F.; Lichtner, Peter C.

    2006-05-31

    This project seeks to improve the basic understanding of the role of colloids in facilitating the transport of contaminants in the vadose zone. We focus on three major thrusts: (1) thermodynamic stability and mobility of colloids formed by reactions of sediments with highly alkaline tank waste solutions, (2) colloid-contaminant interactions, and (3) in-situ colloid mobilization and colloid facilitated contaminant transport occurring in both contaminated and uncontaminated Hanford sediments.

  8. Polarity inversion of ζ-potential in concentrated colloidal dispersions.

    PubMed

    Manzanilla-Granados, Héctor M; Jiménez-Ángeles, Felipe; Lozada-Cassou, Marcelo

    2011-10-27

    A concentrated colloidal dispersion is studied by applying an integral equations theory to the colloidal primitive model fluid. Important effects, attributed to large size and charge and to the finite concentration of colloidal particles, are found. We observe a polarity inversion of ζ-potential for concentrated colloidal dispersions, while it is not present for a single colloidal particle at infinite dilution. An excellent qualitative agreement between our theoretical predictions and our computer simulations is observed. PMID:21928833

  9. Colloidal-sized metal-organic frameworks: synthesis and applications.

    PubMed

    Sindoro, Melinda; Yanai, Nobuhiro; Jee, Ah-Young; Granick, Steve

    2014-02-18

    Colloidal metal-organic frameworks (CMOFs), nanoporous colloidal-sized crystals that are uniform in both size and polyhedral shape, are crystals composed of metal ions and organic bridging ligands, which can be used as building blocks for self-assembly in organic and aqueous liquids. They stand in contrast to conventional metal-organic frameworks (MOFs), which scientists normally study in the form of bulk crystalline powders. However, powder MOFs generally have random crystal size and shape and therefore do not possess either a definite mutual arrangement with adjacent particles or uniformity. CMOFs do have this quality, which can be important in vital uptake and release kinetics. In this Account, we present the diverse methods of synthesis, pore chemistry control, surface modification, and assembly techniques of CMOFs. In addition, we survey recent achievements and future applications in this emerging field. There is potential for a paradigm shift, away from using just bulk crystalline powders, towards using particles whose size and shape are regulated. The concept of colloidal MOFs takes into account that nanoporous MOFs, conventionally prepared in the form of bulk crystalline powders with random crystal size, shape, and orientation, may also form colloidal-sized objects with uniform size and morphology. Furthermore, the traditional MOF functions that depend on porosity present additional control over those MOF functions that depend on pore interactions. They also can enable controlled spatial arrangements between neighboring particles. To begin, we discuss progress regarding synthesis of MOF nano- and microcrystals whose crystal size and shape are well regulated. Next, we review the methods to modify the surfaces with dye molecules and polymers. Dyes are useful when seeking to observe nonluminescent CMOFs in situ by optical microscopy, while polymers are useful to tune their interparticle interactions. Third, we discuss criteria to assess the stability of CMOFs

  10. Nanomaterial surface chemistry design for advancements in capillary electrophoresis modes.

    PubMed

    Ivanov, Michael R; Haes, Amanda J

    2011-01-01

    Tailored surface chemistry impacts nanomaterial function and stability in applications including in various capillary electrophoresis (CE) modes. Although colloidal nanoparticles were first integrated as colouring agents in artwork and pottery over 2000 years ago, recent developments in nanoparticle synthesis and surface modification increased their usefulness and incorporation in separation science. For instance, precise control of surface chemistry is critically important in modulating nanoparticle functionality and stability in dynamic environments. Herein, recent developments in nanomaterial pseudostationary and stationary phases will be summarized. First, nanomaterial core and surface chemistry compositions will be classified. Next, characterization methods will be described and related to nanomaterial function in various CE modes. Third, methods and implications of nanomaterial incorporation into CE will be discussed. Finally, nanoparticle-specific mechanisms likely involved in CE will be related to nanomaterial surface chemistry. Better understanding of surface chemistry will improve nanoparticle design for the integration into separation techniques. PMID:20967383

  11. Computational chemistry

    NASA Technical Reports Server (NTRS)

    Arnold, J. O.

    1987-01-01

    With the advent of supercomputers, modern computational chemistry algorithms and codes, a powerful tool was created to help fill NASA's continuing need for information on the properties of matter in hostile or unusual environments. Computational resources provided under the National Aerodynamics Simulator (NAS) program were a cornerstone for recent advancements in this field. Properties of gases, materials, and their interactions can be determined from solutions of the governing equations. In the case of gases, for example, radiative transition probabilites per particle, bond-dissociation energies, and rates of simple chemical reactions can be determined computationally as reliably as from experiment. The data are proving to be quite valuable in providing inputs to real-gas flow simulation codes used to compute aerothermodynamic loads on NASA's aeroassist orbital transfer vehicles and a host of problems related to the National Aerospace Plane Program. Although more approximate, similar solutions can be obtained for ensembles of atoms simulating small particles of materials with and without the presence of gases. Computational chemistry has application in studying catalysis, properties of polymers, all of interest to various NASA missions, including those previously mentioned. In addition to discussing these applications of computational chemistry within NASA, the governing equations and the need for supercomputers for their solution is outlined.

  12. Colloidal suspension simulates linear dynamic pressure profile

    NASA Technical Reports Server (NTRS)

    Mc Cann, R. J.

    1966-01-01

    Missile nose fairings immersed in colloidal suspension prepared with various specific gravities simulate pressure profiles very similar to those encountered during reentry. Stress and deflection conditions similar to those expected during atmospheric reentry are thus attained in the laboratory.

  13. Mesoscopic modelling of colloids in chiral nematics.

    PubMed

    Ravnik, Miha; Alexander, Gareth P; Yeomans, Julia M; Zumer, Slobodan

    2010-01-01

    We present numerical modelling of colloidal particles in chiral nematics with cubic symmetry (blue phases) within the framework of the Landau-de Gennes free energy. The interaction potential of a single, nano-sized colloidal particle with a -1/2 disclination line is calculated as a generic trapping mechanism for particles within the cholesteric blue phases. The interaction potential is shown to be highly anisotropic and have threefold rotational symmetry. We discuss the equilibration of the colloidal texture with respect to particle positions and the unit cell size of the blue phase. We also describe how preservation of the liquid crystal volume and the number of particles allows blue phase colloidal structures with different unit cell sizes and configurations to be compared numerically. PMID:20158028

  14. Polydispersity effects in colloid-polymer mixtures.

    PubMed

    Liddle, S M; Narayanan, T; Poon, W C K

    2011-05-18

    We study phase separation and transient gelation experimentally in a mixture consisting of polydisperse colloids (polydispersity: ≈ 6%) and non-adsorbing polymers, where the ratio of the average size of the polymer to that of the colloid is ≈ 0.062. Unlike what has been reported previously for mixtures with somewhat lower colloid polydispersity (≈ 5%), the addition of polymers does not expand the fluid-solid coexistence region. Instead, we find a region of fluid-solid coexistence which has an approximately constant width but an unexpected re-entrant shape. We detect the presence of a metastable gas-liquid binodal, which gives rise to two-stepped crystallization kinetics that can be rationalized as the effect of fractionation. Finally, we find that the separation into multiple coexisting solid phases at high colloid volume fractions predicted by equilibrium statistical mechanics is kinetically suppressed before the system reaches dynamical arrest. PMID:21525554

  15. Ultrasonically assisted deposition of colloidal crystals

    SciTech Connect

    Wollmann, Sabine; Patel, Raj B.; Wixforth, Achim; Krenner, Hubert J.

    2014-07-21

    Colloidal particles are a versatile physical system which have found uses across a range of applications such as the simulation of crystal kinetics, etch masks for fabrication, and the formation of photonic band-gap structures. Utilization of colloidal particles often requires a means to produce highly ordered, periodic structures. One approach is the use of surface acoustic waves (SAWs) to direct the self-assembly of colloidal particles. Previous demonstrations using standing SAWs were shown to be limited in terms of crystal size and dimensionality. Here, we report a technique to improve the spatial alignment of colloidal particles using traveling SAWs. Through control of the radio frequency power, which drives the SAW, we demonstrate enhanced quality and dimensionality of the crystal growth. We show that this technique can be applied to a range of particle sizes in the μm-regime and may hold potential for particles in the sub-μm-regime.

  16. A Course in Colloid and Surface Science.

    ERIC Educational Resources Information Center

    Scamehorn, John F.

    1984-01-01

    Describes a course for chemical engineers, chemists, and petroleum engineers that focuses on colloid and surface science. Major topic areas in the course include capillarity, surface thermodynamics, adsorption contact angle, micelle formation, solubilization in micelles, emulsions, foams, and applications. (JN)

  17. Dynamical Threshold of Diluteness of Soft Colloids

    SciTech Connect

    Chen, Wei-Ren; Do, Changwoo; Egami, T; Falus, Peter; Li, Xin; Liu, Dazhi; Porcar, L.; Sanchez-Diaz, Luis E; Smith, Gregory Scott; Wu, Bin

    2014-01-01

    The dynamics of soft colloids in solutions is characterized by internal collective motion as well as center-of-mass diffusion. Using neutron scattering we demonstrate that the competition between the relaxation processes associated with these two degrees of freedom results in strong dependence of dynamics and structure on colloid concentration, c, well below the overlap concentration c*. Triggered by the increasing inter-particle collisions, substantial structural dehydration and slowing-down of internal dynamics occurs before geometrically defined colloidal overlap develops. This observation is surprising since it is generally believed that the internal dynamics and conformation of soft colloidal particles essentially remain invariant below c*. The competition between these two relaxation processes gives rise to a new dynamically-defined dilute threshold concentration well below c*.

  18. Colloidal gold: a pluripotent receptor probe.

    PubMed

    Handley, D A; Chien, S

    1983-10-01

    Colloidal gold is an electron-dense, lyophobic colloid that readily forms a stable electrostatic interaction with a variety of macromolecules. Monodispersed colloids ranging from 3-150 nm in diameter can be produced to provide the researcher with flexibility in selecting the optimally sized probe. Gold labeling of antibodies and lectins has been extensively used to study surface antigens and cell components. Recently, the use of gold labeling has been extended to study receptor-ligand binding, enzyme-substrate reactions, and transcellular pathways. Published applications include gold labeling of metabolites (low-density lipoproteins), enzymes (DNAase and RNAase, RNA polymerase, thrombin, collagenase, elastase), hormones (insulin, epidermal growth factor, glucagon), circulating plasma proteins (asialoglycoprotein, alpha 2-macroglobulin, factor VIII-von Willebrand factor), and endotoxins (tetanus toxin, cholera toxin). This broad spectrum of applications emphasizes the versatility and usefulness of colloidal gold as a probe in areas of cell biology related to receptors, endocytosis, transport, and functions of proteins. PMID:6356133

  19. Self-similarity in active colloid motion

    NASA Astrophysics Data System (ADS)

    Constant, Colin; Sukhov, Sergey; Dogariu, Aristide

    The self-similarity of displacements among randomly evolving systems has been used to describe the foraging patterns of animals and predict the growth of financial systems. At micron scales, the motion of colloidal particles can be analyzed by sampling their spatial displacement in time. For self-similar systems in equilibrium, the mean squared displacement increases linearly in time. However, external forces can take the system out of equilibrium, creating active colloidal systems, and making this evolution more complex. A moment scaling spectrum of the distribution of particle displacements quantifies the degree of self-similarity in the colloid motion. We will demonstrate that, by varying the temporal and spatial characteristics of the external forces, one can control the degree of self-similarity in active colloid motion.

  20. Sulfonated nanoporous colloidal films and membranes

    NASA Astrophysics Data System (ADS)

    Smith, Joanna Jane

    The objective of this thesis is to describe the preparation and investigation of a new class of proton-conducting membrane materials, namely, nanoporous colloidal membranes whose proton conductivity results from the nanopore surface modification with organic molecules carrying acid functionalities. Both the proton transport and ion transport were studied in nanoporous silica colloidal crystals that were surface modified with sulfonic groups. First, the transport of ions was studied through sulfonated silica colloidal films that were supported on platinum electrodes using cyclic voltammetry. The surface of self-assembled nanoporous silica colloidal crystalline films was sulfonated using 1,3-propanesultone. We found that the flux of anions through the sulfonated colloidal films is reduced, while the flux of cations is increased, compared to the unmodified colloidal films. Second, the proton transport in free-standing assemblies of surface-sulfonated silica nanospheres, either randomly packed or self-assembled into a close-packed arrangement, were studied. It was demonstrated that colloidal assemblies prepared using surface-sulfonated silica nanospheres posses proton conductivity that depends on the ordering of the material, temperature and relative humidity. Based on the comparison between the close-packed and disordered assemblies made of the same spheres, we conclude that the increase in structural organization of the self-assembled colloidal materials leads to increased proton conductivity and better water retention. Next free-standing colloidal membranes with a relatively large area and no mechanical defects were prepared by sintering silica colloidal films. The sintered membranes were then surface rehydroxylated, which restores the surface silanol groups, and then can be chemically modified. Finally, sintered self-assembled nanoporous silica colloidal crystals were modified with poly(sulfopropyl-methacrylate) (pSPM) and poly(stryrenesulfonic acid) (pSSA) brushes

  1. Assessing the heteroaggregation of manufactured nanoparticles with geogenic colloids in surface water

    NASA Astrophysics Data System (ADS)

    Labille, Jerome; Slomberg, Danielle; Sani-Kaast, Nicole; Praetorius, Antonia; Ollivier, Patrick; Radakovitch, Olivier; Brant, Jonathan; Scheringer, Martin; Bottero, Jean-Yves

    2014-05-01

    To study and predict the fate of engineered nanoparticles (ENP) in surface water, relevant environmental conditions should be applied, regarding both the system composition and the ENP concentration. This is likely to favour the heteroaggregation of ENPs with naturally occurring colloids. In this work, we studied these interactions in natural surface waters from river (Rhone river, France) and lake (Cholet, France) displaying contrasted organic and inorganic compositions. TiO2 nanoparticles were spiked in these systems, and the kinetics for heteroaggregation was assessed using laser diffraction and particle counting. A model approach was also followed with synthetic water of comparable composition in order to better understand the driving mechanisms. It appeared that, depending on the solution physichal-chemistry (pH, ionic strength) and the nature of major colloids (mineral SPM, natural organic matter), ENPs show a significant affinity for the colloids, which induces rapid heteroaggregation of the system and sedimentation of the aggregates formed. The concentration ratio between ENP and colloid, appears highly determining for this mechanism, a critical ENP concentration being evidenced. These data, coupled to a fate model, will enable to deliver a probability ranking of the potential scenarios on the fate of ENPs in natural aqueous systems at the river scale. This work was conducted in the frame of NANOHETER program, ERA-NET SIINN Call 2012.

  2. Flow-induced alignment of (100) fcc thin film colloidal crystals.

    PubMed

    Joy, Midhun; Muangnapoh, Tanyakorn; Snyder, Mark A; Gilchrist, James F

    2015-09-28

    The realization of structural diversity in colloidal crystals obtained by self-assembly techniques remains constrained by thermodynamic considerations and current limits on our ability to alter structure over large scales using imposed fields and confinement. In this work, a convective-based procedure to fabricate multi-layer colloidal crystal films with extensive square-like symmetry is enabled by periodic substrate motion imposed during the continuous assembly. The formation of film-spanning domains of (100) fcc symmetry as a result of added vibration is robust across a range of micron-scale monosized spherical colloidal suspensions (e.g., polystyrene, silica) as well as substrate surface chemistries (e.g., hydrophobic, hydrophilic). The generation of extensive single crystalline (100) fcc domains as large as 15 mm(2) and covering nearly 40% of the colloidal crystalline film is possible by simply tuning coating conditions and multi-layer film thickness. Preferential orientation of the square-packed domains with respect to the direction of deposition is attributed to domain generation based upon a shear-related mechanism. Visualization during assembly gives clues toward the mechanism of this flow-driven self-assembly method. PMID:26238223

  3. Colloids generation from metallic uranium fuel

    SciTech Connect

    Metz, C.; Fortner, J.; Goldberg, M.; Shelton-Davis, C.

    2000-07-20

    The possibility of colloid generation from spent fuel in an unsaturated environment has significant implications for storage of these fuels in the proposed repository at Yucca Mountain. Because colloids can act as a transport medium for sparingly soluble radionuclides, it might be possible for colloid-associated radionuclides to migrate large distances underground and present a human health concern. This study examines the nature of colloidal materials produced during corrosion of metallic uranium fuel in simulated groundwater at elevated temperature in an unsaturated environment. Colloidal analyses of the leachates from these corrosion tests were performed using dynamic light scattering and transmission electron microscopy. Results from both techniques indicate a bimodal distribution of small discrete particles and aggregates of the small particles. The average diameters of the small, discrete colloids are {approximately}3--12 nm, and the large aggregates have average diameters of {approximately}100--200 nm. X-ray diffraction of the solids from these tests indicates a mineral composition of uranium oxide or uranium oxy-hydroxide.

  4. Sterically stabilized colloids with tunable repulsions.

    PubMed

    van Gruijthuijsen, Kitty; Obiols-Rabasa, Marc; Heinen, Marco; Nägele, Gerhard; Stradner, Anna

    2013-09-10

    When studying tunable electrostatic repulsions in aqueous suspensions of charged colloids, irreversible colloid aggregation or gelation may occur at high salt concentrations. For many commonly used synthetic colloids, such as polystyrene and silica particles, the reason for coagulation is the presence of unbalanced, strongly attractive, and short-ranged van der Waals (VDW) forces. Here, we present an aqueous polystyrene model colloid that is sterically stabilized against VDW attractions. We show that the synthesis procedure, based on a neutral initiator couple and a nonionic surfactant, introduces surface charges that can be further increased by the addition of charged comonomer methacrylic acid. Thus, the interactions between the polystyrene spheres can be conveniently tuned from hard-sphere-like to charge-stabilized with long-ranged electrostatic repulsions described by a Yukawa-type pair potential. The particle size, grafting density, core-shell structure, and surface charge are characterized by light and neutron scattering. Using X-ray and neutron scattering in combination with an accurate analytic integral equation scheme for the colloidal static structure factor, we deduce effective particle charges for colloid volume fractions ≥0.1 and salt concentrations in the range of 1.5 to 50 mM. PMID:23937718

  5. Self-replication with magnetic dipolar colloids

    NASA Astrophysics Data System (ADS)

    Dempster, Joshua M.; Zhang, Rui; Olvera de la Cruz, Monica

    2015-10-01

    Colloidal self-replication represents an exciting research frontier in soft matter physics. Currently, all reported self-replication schemes involve coating colloidal particles with stimuli-responsive molecules to allow switchable interactions. In this paper, we introduce a scheme using ferromagnetic dipolar colloids and preprogrammed external magnetic fields to create an autonomous self-replication system. Interparticle dipole-dipole forces and periodically varying weak-strong magnetic fields cooperate to drive colloid monomers from the solute onto templates, bind them into replicas, and dissolve template complexes. We present three general design principles for autonomous linear replicators, derived from a focused study of a minimalist sphere-dimer magnetic system in which single binding sites allow formation of dimeric templates. We show via statistical models and computer simulations that our system exhibits nonlinear growth of templates and produces nearly exponential growth (low error rate) upon adding an optimized competing electrostatic potential. We devise experimental strategies for constructing the required magnetic colloids based on documented laboratory techniques. We also present qualitative ideas about building more complex self-replicating structures utilizing magnetic colloids.

  6. Self-replication with magnetic dipolar colloids.

    PubMed

    Dempster, Joshua M; Zhang, Rui; Olvera de la Cruz, Monica

    2015-10-01

    Colloidal self-replication represents an exciting research frontier in soft matter physics. Currently, all reported self-replication schemes involve coating colloidal particles with stimuli-responsive molecules to allow switchable interactions. In this paper, we introduce a scheme using ferromagnetic dipolar colloids and preprogrammed external magnetic fields to create an autonomous self-replication system. Interparticle dipole-dipole forces and periodically varying weak-strong magnetic fields cooperate to drive colloid monomers from the solute onto templates, bind them into replicas, and dissolve template complexes. We present three general design principles for autonomous linear replicators, derived from a focused study of a minimalist sphere-dimer magnetic system in which single binding sites allow formation of dimeric templates. We show via statistical models and computer simulations that our system exhibits nonlinear growth of templates and produces nearly exponential growth (low error rate) upon adding an optimized competing electrostatic potential. We devise experimental strategies for constructing the required magnetic colloids based on documented laboratory techniques. We also present qualitative ideas about building more complex self-replicating structures utilizing magnetic colloids. PMID:26565238

  7. Autonomous colloidal crystallization in a galvanic microreactor

    NASA Astrophysics Data System (ADS)

    Punckt, Christian; Jan, Linda; Jiang, Peng; Frewen, Thomas A.; Saville, Dudley A.; Kevrekidis, Ioannis G.; Aksay, Ilhan A.

    2012-10-01

    We report on a technique that utilizes an array of galvanic microreactors to guide the assembly of two-dimensional colloidal crystals with spatial and orientational order. Our system is comprised of an array of copper and gold electrodes in a coplanar arrangement, immersed in a dilute hydrochloric acid solution in which colloidal micro-spheres of polystyrene and silica are suspended. Under optimized conditions, two-dimensional colloidal crystals form at the anodic copper with patterns and crystal orientation governed by the electrode geometry. After the aggregation process, the colloidal particles are cemented to the substrate by co-deposition of reaction products. As we vary the electrode geometry, the dissolution rate of the copper electrodes is altered. This way, we control the colloidal motion as well as the degree of reaction product formation. We show that particle motion is governed by a combination of electrokinetic effects acting directly on the colloidal particles and bulk electrolyte flow generated at the copper-gold interface.

  8. Linked topological colloids in a nematic host.

    PubMed

    Martinez, Angel; Hermosillo, Leonardo; Tasinkevych, Mykola; Smalyukh, Ivan I

    2015-04-14

    Geometric shape and topology of constituent particles can alter many colloidal properties such as Brownian motion, self-assembly, and phase behavior. Thus far, only single-component building blocks of colloids with connected surfaces have been studied, although topological colloids, with constituent particles shaped as freestanding knots and handlebodies of different genus, have been recently introduced. Here we develop a topological class of colloids shaped as multicomponent links. Using two-photon photopolymerization, we fabricate colloidal microparticle analogs of the classic examples of links studied in the field of topology, the Hopf and Solomon links, which we disperse in nematic fluids that possess orientational ordering of anisotropic rod-like molecules. The surfaces of these particles are treated to impose tangential or perpendicular boundary conditions for the alignment of liquid crystal molecules, so that they generate a host of topologically nontrivial field and defect structures in the dispersing nematic medium, resulting in an elastic coupling between the linked constituents. The interplay between the topologies of surfaces of linked colloids and the molecular alignment field of the nematic host reveals that linking of particle rings with perpendicular boundary conditions is commonly accompanied by linking of closed singular defect loops, laying the foundations for fabricating complex composite materials with interlinking-based structural organization. PMID:25825765

  9. Colloidal diffusion over a periodic energy landscape

    NASA Astrophysics Data System (ADS)

    Ma, Xiao-Guang; Lai, Pik-Yin; Tong, Penger

    2014-03-01

    A two-layer colloidal system is developed for the study of colloidal diffusion over a two-dimensional periodic energy landscape. The energy landscape is made from the bottom layer of colloidal spheres forming a honey-comb crystalline pattern above a glass substrate. The corrugated surface of the bottom colloidal crystal provides a gravitational potential field for the diffusing particles in the top layer. The obtained population probability histogram P(x , y) of the diffusing particles is used to fully characterize the energy landscape U(x , y) via the Boltzmann distribution. The dynamical properties of the diffusing particle, such as its escape time tR and diffusion coefficient D are simultaneously measured from the particle's trajectories. The long-time diffusion coefficients D is found to be in good agreement with the theory for all colloidal samples studied. The experiment demonstrates the applications of this newly constructed colloidal energy landscape. *Work supported in part by the Research Grants Council of Hong Kong SAR.

  10. Inventions Utilizing Microfluidics and Colloidal Particles

    NASA Technical Reports Server (NTRS)

    Marr, David W.; Gong, Tieying; Oakey, John; Terray, Alexander V.; Wu, David T.

    2009-01-01

    Several related inventions pertain to families of devices that utilize microfluidics and/or colloidal particles to obtain useful physical effects. The families of devices can be summarized as follows: (1) Microfluidic pumps and/or valves wherein colloidal-size particles driven by electrical, magnetic, or optical fields serve as the principal moving parts that propel and/or direct the affected flows. (2) Devices that are similar to the aforementioned pumps and/or valves except that they are used to manipulate light instead of fluids. The colloidal particles in these devices are substantially constrained to move in a plane and are driven to spatially order them into arrays that function, variously, as waveguides, filters, or switches for optical signals. (3) Devices wherein the ultra-laminar nature of microfluidic flows is exploited to effect separation, sorting, or filtering of colloidal particles or biological cells in suspension. (4) Devices wherein a combination of confinement and applied electrical and/or optical fields forces the colloidal particles to become arranged into three-dimensional crystal lattices. Control of the colloidal crystalline structures could be exploited to control diffraction of light. (5) Microfluidic devices, incorporating fluid waveguides, wherein switching of flows among different paths would be accompanied by switching of optical signals.

  11. Linked topological colloids in a nematic host

    PubMed Central

    Martinez, Angel; Hermosillo, Leonardo; Tasinkevych, Mykola; Smalyukh, Ivan I.

    2015-01-01

    Geometric shape and topology of constituent particles can alter many colloidal properties such as Brownian motion, self-assembly, and phase behavior. Thus far, only single-component building blocks of colloids with connected surfaces have been studied, although topological colloids, with constituent particles shaped as freestanding knots and handlebodies of different genus, have been recently introduced. Here we develop a topological class of colloids shaped as multicomponent links. Using two-photon photopolymerization, we fabricate colloidal microparticle analogs of the classic examples of links studied in the field of topology, the Hopf and Solomon links, which we disperse in nematic fluids that possess orientational ordering of anisotropic rod-like molecules. The surfaces of these particles are treated to impose tangential or perpendicular boundary conditions for the alignment of liquid crystal molecules, so that they generate a host of topologically nontrivial field and defect structures in the dispersing nematic medium, resulting in an elastic coupling between the linked constituents. The interplay between the topologies of surfaces of linked colloids and the molecular alignment field of the nematic host reveals that linking of particle rings with perpendicular boundary conditions is commonly accompanied by linking of closed singular defect loops, laying the foundations for fabricating complex composite materials with interlinking-based structural organization. PMID:25825765

  12. Tunable Time-Dependent Colloidal Interactions

    NASA Astrophysics Data System (ADS)

    Bergman, Andrew M.; Rogers, W. Benjamin; Manoharan, Vinothan N.

    Self-assembly of colloidal particles can be driven by changes in temperature, density, or the concentration of solutes, and it is even possible to program the thermal response and equilibrium phase transitions of such systems. It is still difficult, however, to tune how the self-assembly process varies in time. We demonstrate control over the time-dependence of colloidal interactions, using DNA-functionalized colloidal particles with binding energies that are set by the concentration of a free linker strand in solution. We control the rate at which this free strand is consumed using a catalytic DNA reaction, whose rate is governed by the concentration of a catalyst strand. Varying the concentration of the linker, its competitor, and the catalyst at a fixed temperature, we can tune the rate and degree of the formation of colloidal aggregates and their following disassembly. Close to the colloidal melting point, the timescales of these out-of-equilibrium assembly and disassembly processes are determined by the rate of the catalytic reaction. Far below the colloidal melting point, however, the effects from varying our linker and competitor concentrations dominate.

  13. Interactions between radioactively labeled colloids and natural particles: Evidence for colloidal pumping

    SciTech Connect

    Wen, L.S.; Santschi, P.H.; Tang, D.

    1997-07-01

    It has been hypothesized that colloidal forms of trace metals can be reactive intermediaries in the scavenging processes leading to the removal of their particulate forms. A series of radiotracer experiments using natural colloidal organic matter from Galveston Bay, USA were carried out in order to test this hypothesis. Suspended particle uptake of originally colloidally bound trace metals occurred in a matter of hours to days in estuarine waters. After ten days, the majority ( >50%) of the colloidal trace metals had been transferred into the particulate phase ({ge} 0.45{mu}m), except for {sup 65}Zn. Two distinctively different temporal regions of removal of colloidal trace metals were identified: a faster reaction during the first four hours, followed by a slower reaction after approximately one day. In a separate river water-seawater mixing experiment, the solid/solution partitioning of the radiotracers was investigated in the absence of suspended matter. About 30% of most of the elements, except Ag and Fe ({approximately}60%), were associated with a newly formed particulate phase after eight days. There were two major trends: (1) the particulate fraction of {sup 59}Fe and {sup 110}Ag increased while the colloidal fraction decreased, suggesting a colloidal pumping mechanism. (2) The particulate fraction of {sup 54}Mn, {sup 133}Ba, {sup 65}Zn, {sup 109}Cd, {sup 113}Sn, and {sup 60}Co increased while the LMW({le}1 kDa) fraction decreased, suggesting a direct uptake into the particulate fraction with less involvement of a transitory colloidal phase. The results from these experiments suggested two different pathways for colloidal tracer uptake by particles: (1) colloidal pumping of a major component (e.g., biopolymer) of the colloidal pool and (2) coagulation of trace components (e.g., phytochelatins) with varying affinities for different trace metals. 39 refs., 8 figs., 3 tabs.

  14. The redox potential of Pu containing acidic solutions and the fate of "Pu(IV)-colloids": Direct measurement versus optical absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Icker, M.; Walther, C.; Neck, V.; Geckeis, H.

    2010-03-01

    Redox potentials were measured in acidic aqueous solutions (-log10[H+]=0.7) containing different fractions of tri- and tetravalent plutonium. Eh values measured directly by a Pt electrode vs Ag/AgCl reference electrode agree very well with the redox potential calculated from the oxidation state distribution Pu(III)/Pu(IV). By monitoring the solutions over 120 days the kinetics of redox state distribution and dissolution of initially present Pu(IV)-colloids were studied. In solutions of Eh>950mV colloids dissolve and form Pu(VI), whereas at lower Eh the dissolution of colloids leads to formation of Pu(III). These findings corroborate the assumption that colloids are an integral part of the aqueous Pu redox chemistry and that formation and dissolution can be fully understood by means of Eh / pH stability calculations.

  15. Magnetic nanostructures by colloidal lithography

    NASA Astrophysics Data System (ADS)

    Zhu, Frank Qing

    Structural, magnetic and in some cases magneto-transport properties of (1) symmetric and asymmetric ferromagnetic nanorings and (2) single layer, multilayer, and exchange biased ferromagnetic nanodots prepared by colloidal lithography are presented. A fast, reliable and cost effective method has been developed to fabricate large number (˜ 109) of magnetic nanorings over macroscopic areas (˜ cm2) with large areal densities (up to 45 rings/mum 2). Cobalt nanorings with diameters ranging from 100 nm to 500 nm have been fabricated by sputtering Co onto nanosphere-coated substrates followed by ion beam etching. X-ray diffraction verifies that the Co nanorings still have hexagonal close-packed (hcp) structure. Scanning electron microscopy reveals that the cross-section of the symmetric nanoring is tapered and uniform along the circumference, and the cross-section of the asymmetric nanoring changes progressively along the circumference. Two magnetic reversal processes have been found in magnetic nanorings---the vortex formation process and the onion rotation process. The co-existence of these two processes is the manifestation of the competition between the exchange energy and the magnetostatic energy in the nanorings. Micromagnetics simulations have been carried out to reveal the details of the magnetic reversals. The experimental and the computed hysteresis loops agree both qualitatively and quantitatively. For the 100 nm symmetric Co nanorings, the vortex formation process has a probability of about 40%, while the onion rotation process has 60% chances. To increase the probability of vortex formation process, a desirable process for application, asymmetric nanorings have been fabricated by ion beam etching at oblique angles. Unlike the symmetric nanorings, the probability of the vortex formation process in asymmetric nanorings can be controlled by the direction of the external field. For the 100 nm asymmetric nanorings, the fraction of the vortex formation process

  16. Statistical thermodynamics of charge-stabilized colloids

    NASA Astrophysics Data System (ADS)

    Torres Valderrama, A.

    2008-06-01

    This thesis is a theoretical study of equilibrium statistical thermodynamic properties of colloidal systems in which electrostatic interactions play a dominant role, namely, charge-stabilized colloidal suspensions. Such systems are fluids consisting of a mixture of a large number of mesoscopic particles and microscopic ions which interact via the Coulomb force, suspended in a molecular fluid. Quantum statistical mechanics is essential to fully understand the properties and stability of such systems. A less fundamental but for many purposes, sufficient description, is provided by classical statistical mechanics. In such approximation the system is considered as composed of a great number of charged classical particles with additional hard-core repulsions. The kinetic energy or momentum integrals become independent Gaussians, and hence their contribution to the free energy can be trivially evaluated. The contribution of the potential energy to the free energy on the other hand, depends upon the configuration of all the particles and becomes highly non-trivial due to the long-range character of the Coulomb force and the extremely different length scales involved in the problem. Using the microscopic model described above, we focus on the calculation of equilibrium thermodynamic properties (response functions), correlations (structure factors), and mechanical properties (forces and stresses), which can be measured in experiments and computed by Monte Carlo simulations. This thesis is divided into three parts. In part I, comprising chapters 2 and 3, we focus on finite-thickness effects in colloidal platelets and rigid planar membranes. In chapter 2 we study electrolyte-mediated interactions between two of such colloidal objects. Several aspects of these interactions are considered including the nature (attractive or repulsive) of the force between the objects, the osmotic properties for different types of surfaces and image charge effects. In part II, which includes

  17. (Pesticide chemistry)

    SciTech Connect

    Barnthouse, L.W.

    1990-09-04

    This report summarizes a trip by L. W. Barnthouse of the Environmental Sciences Division (ESD), Oak Ridge National Laboratory (ORNL), to Hamburg, Federal Republic of Germany (FRG), where he participated in the 7th International Congress of Pesticide Chemistry. He chaired a workshop on experimental systems for determining effects of pesticides on nontarget organisms and gave an oral presentation at a symposium on pesticide risk assessment. Before returning to the United States, Dr. Barnthouse visited the Netherlands Institute for Sea Research in Texel, the Netherlands.

  18. Colloidal Gelation-2 and Colloidal Disorder-Order Transition-2 Investigations Conducted on STS-95

    NASA Technical Reports Server (NTRS)

    Hoffmann, Monica T.

    2000-01-01

    The Colloidal Gelation-2 (CGEL 2) and Colloidal Disorder-Order Transition-2 (CDOT 2) investigations flew on Space Shuttle Discovery mission STS-95 (also known as the John Glenn Mission). These investigations were part of a series of colloid experiments designed to help scientists answer fundamental science questions and reduce the trial and error involved in developing new and better materials. Industries dealing with semiconductors, electro-optics, ceramics, and composites are just a few that may benefit from this knowledge. The goal of the CGEL 2 investigation was to study the fundamental properties of colloids to help scientists better understand their nature and make them more useful for technology. Colloids consist of very small (submicron) particles suspended in a fluid. They play a critical role in the technology of this country, finding uses in materials ranging from paints and coatings to drugs, cosmetics, food, and drink. Although these products are routinely produced and used, there are still many aspects of their behavior about which scientists know little. Understanding their structures may allow scientists to manipulate the physical properties of colloids (a process called "colloidal engineering") to produce new materials and products. Colloid research may even improve the processing of known products to enhance their desirable properties.

  19. Colloids in the River Inn

    NASA Astrophysics Data System (ADS)

    Ueckert, Martina; Baumann, Thomas

    2014-05-01

    In the light of an increasing number of technical applications using nanoparticles and reports of adverse effects of engineered nanoparticles, research on the occurrence and stability of particles in all compartments has to be intensified. Colloids in river water represent the geologic setting, environmental conditions, and the anthropogenic use in its catchment. The river not only acts as a sink for nanoparticles but also as the source term due to exchange in the hyporheic zone and in bank filtration setups. The concentration, size distribution and elemental composition of particles in the River Inn were studied from the source in the Swiss Alps to the river mouth at Passau. Samples were collected after each tributary from a sub-catchment and filtered on-site. The elemental composition was determined after acid digestion with ICP/MS. SEM/EDX analyses provided morphological and elemental information for single particles. A complementary chemical analysis of the river water was performed to assess the geochemical stability of indvidual particles. Particles in the upper, rural parts mainly reveal changes in the geological setting of the tributary catchments. Not unexpectedly, particles originating from crystalline rocks, were more stable than particles originating from calcareous rocks. Anthropogenic and industrial influences increase in the lower parts. This went together with a change of the size distribution, an increase of the number of organic particles, and a decrease of the microfauna. Interestingly, specific leisure activities in a sub-catchment, like extensive downhill skiing, manifest itself in the particle composition.

  20. Colloidal Bandpass and Bandgap Filters

    NASA Astrophysics Data System (ADS)

    Yellen, Benjamin; Tahir, Mukarram; Ouyang, Yuyu; Nori, Franco

    2013-03-01

    Thermally or deterministically-driven transport of objects through asymmetric potential energy landscapes (ratchet-based motion) is of considerable interest as models for biological transport and as methods for controlling the flow of information, material, and energy. Here, we provide a general framework for implementing a colloidal bandpass filter, in which particles of a specific size range can be selectively transported through a periodic lattice, whereas larger or smaller particles are dynamically trapped in closed-orbits. Our approach is based on quasi-static (adiabatic) transition in a tunable potential energy landscape composed of a multi-frequency magnetic field input signal with the static field of a spatially-periodic magnetization. By tuning the phase shifts between the input signal and the relative forcing coefficients, large-sized particles may experience no local energy barriers, medium-sized particles experience only one local energy barrier, and small-sized particles experience two local energy barriers. The odd symmetry present in this system can be used to nudge the medium-sized particles along an open pathway, whereas the large or small beads remain trapped in a closed-orbit, leading to a bandpass filter, and vice versa for a bandgap filter. NSF CMMI - 0800173, Youth 100 Scholars Fund

  1. Seismic stress mobilization of natural colloids in a porous rock

    SciTech Connect

    Roberts, Peter M; Abdel-fattah, Amr I

    2008-01-01

    Stress oscillations at 26 Hz enhanced the release of natural micro-particles (colloids) in a porous rock sample. Micron-scale effects were induced by meter-scale wavelengths. The results are attributed to altering the release rate coefficient for colloids trapped in pores. The rate change did not depend on colloid size and thus is not due to altering colloid-pore-wall interactions. Enhanced colloid detachment from pore walls and flushing from dead-end pores are likely mechanisms. This phenomenon could impact a broad range of physical sciences involving colloid dynamics and porous transport.

  2. Versatile Aerogel Fabrication by Freezing and Subsequent Freeze-Drying of Colloidal Nanoparticle Solutions.

    PubMed

    Freytag, Axel; Sánchez-Paradinas, Sara; Naskar, Suraj; Wendt, Natalja; Colombo, Massimo; Pugliese, Giammarino; Poppe, Jan; Demirci, Cansunur; Kretschmer, Imme; Bahnemann, Detlef W; Behrens, Peter; Bigall, Nadja C

    2016-01-18

    A versatile method to fabricate self-supported aerogels of nanoparticle (NP) building blocks is presented. This approach is based on freezing colloidal NPs and subsequent freeze drying. This means that the colloidal NPs are directly transferred into dry aerogel-like monolithic superstructures without previous lyogelation as would be the case for conventional aerogel and cryogel fabrication methods. The assembly process, based on a physical concept, is highly versatile: cryogelation is applicable for noble metal, metal oxide, and semiconductor NPs, and no impact of the surface chemistry or NP shape on the resulting morphology is observed. Under optimized conditions the shape and volume of the liquid equal those of the resulting aerogels. Also, we show that thin and homogeneous films of the material can be obtained. Furthermore, the physical properties of the aerogels are discussed. PMID:26638874

  3. The Dynamic Organic/Inorganic Interface of Colloidal PbS Quantum Dots.

    PubMed

    Grisorio, Roberto; Debellis, Doriana; Suranna, Gian Paolo; Gigli, Giuseppe; Giansante, Carlo

    2016-06-01

    Colloidal quantum dots are composed of nanometer-sized crystallites of inorganic semiconductor materials bearing organic molecules at their surface. The organic/inorganic interface markedly affects forms and functions of the quantum dots, therefore its description and control are important for effective application. Herein we demonstrate that archetypal colloidal PbS quantum dots adapt their interface to the surroundings, thus existing in solution phase as equilibrium mixtures with their (metal-)organic ligand and inorganic core components. The interfacial equilibria are dictated by solvent polarity and concentration, show striking size dependence (leading to more stable ligand/core adducts for larger quantum dots), and selectively involve nanocrystal facets. This notion of ligand/core dynamic equilibrium may open novel synthetic paths and refined nanocrystal surface-chemistry strategies. PMID:27038221

  4. Evaluation of Colloid Retention Site Dominance in Variably Saturated Porous Media: An All Pores Pore-Scale Analysis

    NASA Astrophysics Data System (ADS)

    Morales, Veronica; Perez-Reche, Francisco; Holzner, Markus; Kinzelbach, Wolfgang

    2016-04-01

    It is well accepted that colloid and nanoparticle transport processes in porous media differ substantially between water saturated and unsaturated conditions. Differences are frequently ascribed to particle immobilization by association with interfaces with the gas, as well as to restrictions of the liquid medium through which colloids are transported. Yet, the current understanding of the importance of particle retention at gas interfaces is based on observations of single pores or two-dimensional pore network representations, leaving open the question of their statistical significance when all pores in the medium are considered. In order to address this question, column experiments were performed using a model porous medium of glass beads through which Silver particles were transported for conditions of varying water content and water chemistry. X-ray microtomography was subsequently employed as a non-destructive imaging technique to obtain pore-scale information of the entire column regarding: i) the presence and distribution of the main locations where colloids can become retained (interfaces with the water-solid, air-water, air-solid, and air-water-solid, grain-grain contacts, and the bulk liquid), ii) deposition profiles of colloids along the column classified by the available retention location, and iii) channel widths of 3-dimensional pore-water network representations. The results presented provide a direct statistical evaluation on the significance of colloid retention by attachment to interfaces or by strainig at contact points where multiple interfaces meet.

  5. Processing pathway dependence of amorphous silica nanoparticle toxicity: colloidal vs pyrolytic.

    PubMed

    Zhang, Haiyuan; Dunphy, Darren R; Jiang, Xingmao; Meng, Huan; Sun, Bingbing; Tarn, Derrick; Xue, Min; Wang, Xiang; Lin, Sijie; Ji, Zhaoxia; Li, Ruibin; Garcia, Fred L; Yang, Jing; Kirk, Martin L; Xia, Tian; Zink, Jeffrey I; Nel, Andre; Brinker, C Jeffrey

    2012-09-26

    We have developed structure/toxicity relationships for amorphous silica nanoparticles (NPs) synthesized through low-temperature colloidal (e.g., Stöber silica) or high-temperature pyrolysis (e.g., fumed silica) routes. Through combined spectroscopic and physical analyses, we have determined the state of aggregation, hydroxyl concentration, relative proportion of strained and unstrained siloxane rings, and potential to generate hydroxyl radicals for Stöber and fumed silica NPs with comparable primary particle sizes (16 nm in diameter). On the basis of erythrocyte hemolytic assays and assessment of the viability and ATP levels in epithelial and macrophage cells, we discovered for fumed silica an important toxicity relationship to postsynthesis thermal annealing or environmental exposure, whereas colloidal silicas were essentially nontoxic under identical treatment conditions. Specifically, we find for fumed silica a positive correlation of toxicity with hydroxyl concentration and its potential to generate reactive oxygen species (ROS) and cause red blood cell hemolysis. We propose fumed silica toxicity stems from its intrinsic population of strained three-membered rings (3MRs) along with its chainlike aggregation and hydroxyl content. Hydrogen-bonding and electrostatic interactions of the silanol surfaces of fumed silica aggregates with the extracellular plasma membrane cause membrane perturbations sensed by the Nalp3 inflammasome, whose subsequent activation leads to secretion of the cytokine IL-1β. Hydroxyl radicals generated by the strained 3MRs in fumed silica, but largely absent in colloidal silicas, may contribute to the inflammasome activation. Formation of colloidal silica into aggregates mimicking those of fumed silica had no effect on cell viability or hemolysis. This study emphasizes that not all amorphous silicas are created equal and that the unusual toxicity of fumed silica compared to that of colloidal silica derives from its framework and surface

  6. Processing pathway dependence of amorphous silica nanoparticle toxicity - colloidal versus pyrolytic

    PubMed Central

    Zhang, Haiyuan; Dunphy, Darren R.; Jiang, Xingmao; Meng, Huan; Sun, Bingbing; Tarn, Derrick; Xue, Min; Wang, Xiang; Lin, Sijie; Ji, Zhaoxia; Li, Ruibin; Garcia, Fred L.; Yang, Jing; Kirk, Martin L.; Xia, Tian; Zink, Jeffrey I; Nel, Andre; Brinker, C. Jeffrey

    2012-01-01

    We have developed structure/toxicity relationships for amorphous silica nanoparticles (NPs) synthesized through low temperature, colloidal (e.g. Stöber silica) or high temperature pyrolysis (e.g. fumed silica) routes. Through combined spectroscopic and physical analyses, we have determined the state of aggregation, hydroxyl concentration, relative proportion of strained and unstrained siloxane rings, and potential to generate hydroxyl radicals for Stöber and fumed silica NPs with comparable primary particle sizes (16-nm in diameter). Based on erythrocyte hemolytic assays and assessment of the viability and ATP levels in epithelial and macrophage cells, we discovered for fumed silica an important toxicity relationship to post-synthesis thermal annealing or environmental exposure, whereas colloidal silicas were essentially non-toxic under identical treatment conditions. Specifically, we find for fumed silica a positive correlation of toxicity with hydroxyl concentration and its potential to generate reactive oxygen species (ROS) and cause red blood cell hemolysis. We propose fumed silica toxicity stems from its intrinsic population of strained three-membered rings (3MRs) along with its chain-like aggregation and hydroxyl content. Hydrogen-bonding and electrostatic interactions of the silanol surfaces of fumed silica aggregates with the extracellular plasma membrane cause membrane perturbations sensed by the Nalp3 inflammasome, whose subsequent activation leads to secretion of the cytokine IL-1β. Hydroxyl radicals generated by the strained 3MRs in fumed silica but largely absent in colloidal silicas may contribute to the inflammasome activation. Formation of colloidal silica into aggregates mimicking those of fumed silica had no effect on cell viability or hemolysis. This study emphasizes that not all amorphous silica is created equal and that the unusual toxicity of fumed silica compared to colloidal silica derives from its framework and surface chemistry along

  7. Interparticle interactions and polarization effects in colloids

    SciTech Connect

    Hayter, J.B.

    1987-01-01

    The physics of simple colloidal systems is usually dominated by three independent length scales: the particle size, the average interparticle distance, and the range of the interparticle potential. The dispersed particles typically have characteristic dimensions in the range 5 to 100 nm, often with spherical or cylindrical symmetry. Dispersion densities vary over volume fractions ranging from 0.5 to 10/sup -4/, with the corresponding mean interparticle distances ranging from about 1 to 10 diameters (in spherical systems). The interaction potential may be very short ranged (hard sphere), very long ranged (Coulomb or dipolar), or anywhere in between (screened Coulomb), and the correlations exhibited in the dispersion may be gas-like, liquid-like or crystalline, depending on the range of the potential relative to the interparticle distance. This rich phase behavior is responsible for the remarkable importance of colloidal studies in many areas of condensed matter physics and biophysics, but it poses often intractable problems in developing the statistical mechanical descriptions necessary for an understanding of scattering data from colloids. This paper will review the considerable recent progress in this field, in the context of SANS experiments on colloids in which the potentials are dominated by either screened Coulomb or magnetic dipolar interactions; in the case of magnetic colloids (ferrofluids), the use of polarization analysis will also be discussed. 32 refs., 4 figs.

  8. Diffusing colloidal probes of cell surfaces.

    PubMed

    Duncan, Gregg A; Fairbrother, D Howard; Bevan, Michael A

    2016-05-25

    Measurements and analyses are reported to quantify dynamic and equilibrium interactions between colloidal particles and live cell surfaces using dark field video microscopy. Two-dimensional trajectories of micron-sized polyethylene glycol (PEG)-coated silica colloids relative to adherent epithelial breast cancer cell perimeters are determined allowing measurement of position dependent diffusivities and interaction potentials. PEG was chosen as the material system of interest to assess non-specific interactions with cell surfaces and establishes a basis for investigation of specific interactions in future studies. Analysis of measured potential energies on cell surfaces reveals the spatial dependence in cell topography. With the measured cell topography and models for particle-cell surface hydrodynamic interactions, excellent agreement is obtained between theoretical and measured colloidal transport on cell surfaces. Quantitative analyses of association lifetimes showed that PEG coatings act to stabilize colloids above the cell surface through net repulsive, steric interactions. Our results demonstrate a self-consistent analysis of diffusing colloidal probe interactions due to conservative and non-conservative forces to characterize biophysical cell surface properties. PMID:27117575

  9. Method for electrohydrodynamically assembling patterned colloidal structures

    NASA Technical Reports Server (NTRS)

    Trau, Mathias (Inventor); Aksay, Ilhan A. (Inventor); Saville, Dudley A. (Inventor)

    1999-01-01

    A method apparatus is provided for electrophoretically depositing particles onto an electrode, and electrohydrodynamically assembling the particles into crystalline structures. Specifically, the present method and apparatus creates a current flowing through a solution to cause identically charged electrophoretically deposited colloidal particles to attract each other over very large distances (<5 particle diameters) on the surface of electrodes to form two-dimensional colloidal crystals. The attractive force can be created with both DC and AC fields and can modulated by adjusting either the field strength or frequency of the current. Modulating this lateral attraction between the particles causes the reversible formation of two-dimensional fluid and crystalline colloidal states on the electrode surface. Further manipulation allows for the formation of two or three-dimensional colloidal crystals, as well as more complex designed structures. Once the required structures are formed, these three-dimension colloidal crystals can be permanently frozen or glued by controlled coagulation induced by to the applied field to form a stable crystalline structure.

  10. Apparatus for electrohydrodynamically assembling patterned colloidal structures

    NASA Technical Reports Server (NTRS)

    Trau, Mathias (Inventor); Aksay, Ilhan A. (Inventor); Saville, Dudley A. (Inventor)

    2000-01-01

    A method apparatus is provided for electrophoretically depositing particles onto an electrode, and electrohydrodynamically assembling the particles into crystalline structures. Specifically, the present method and apparatus creates a current flowing through a solution to cause identically charged electrophoretically deposited colloidal particles to attract each other over very large distances (<5 particle diameters) on the surface of electrodes to form two-dimensional colloidal crystals. The attractive force can be created with both DC and AC fields and can modulated by adjusting either the field strength or frequency of the current. Modulating this lateral attraction between the particles causes the reversible formation of two-dimensional fluid and crystalline colloidal states on the electrode surface. Further manipulation allows for the formation of two or three-dimensional colloidal crystals, as well as more complex designed structures. Once the required structures are formed, these three-dimension colloidal crystals can be permanently frozen or glued by controlled coagulation induced by to the applied field to form a stable crystalline structure.

  11. Colloidal spirals in nematic liquid crystals.

    PubMed

    Senyuk, Bohdan; Pandey, Manoj B; Liu, Qingkun; Tasinkevych, Mykola; Smalyukh, Ivan I

    2015-12-01

    One of the central experimental efforts in nematic colloids research aims to explore how the interplay between the geometry of particles along with the accompanying nematic director deformations and defects around them can provide a means of guiding particle self-assembly and controlling the structure of particle-induced defects. In this work, we design, fabricate, and disperse low-symmetry colloidal particles with shapes of spirals, double spirals, and triple spirals in a nematic fluid. These spiral-shaped particles, which are controlled by varying their surface functionalization to provide tangential or perpendicular boundary conditions of the nematic molecular alignment, are found inducing director distortions and defect configurations with non-chiral or chiral symmetry. Colloidal particles also exhibit both stable and metastable multiple orientational states in the nematic host, with a large number of director configurations featuring both singular and solitonic nonsingular topological defects accompanying them, which can result in unusual forms of colloidal self-assembly. Our findings directly demonstrate how the symmetry of particle-generated director configurations can be further lowered, or not, as compared to the low point group symmetry of solid micro-inclusions, depending on the nature of induced defects while satisfying topological constraints. We show that achiral colloidal particles can cause chiral symmetry breaking of elastic distortions, which is driven by complex three-dimensional winding of induced topological line defects and solitons. PMID:26358649

  12. Colloids with continuously tunable surface charge.

    PubMed

    van Ravensteijn, Bas G P; Kegel, Willem K

    2014-09-01

    In this paper, we present a robust way to tune the surface potential of polystyrene colloids without changing the pH, ionic strength, etc. The colloids are composed of a cross-linked polystyrene core and a cross-linked vinylbenzyl chloride layer. Besides the chlorine groups, the particle surface contains sulfate/sulfonate groups (arising from the polymerization initiators) that provide a negative surface potential. Performing a Menschutkin reaction on the surface chlorine groups with tertiary amines allows us to introduce quaternary, positively charged amines. The overall charge on the particles is then determined by the ratio between the sulfate/sulfonate moieties and the quaternary amines. Using this process, we were able to invert the charge in a continuous manner without losing colloidal stability upon passing the isoelectric point. The straightforward reaction mechanism together with the fact that the reaction could be quenched rapidly resulted in a colloidal system in which the ζ potential can be tuned between -80 and 45 mV. As proof of principle, the positively charged particles were used in heterocoagulation experiments with nanometer- and micrometer-sized negatively charged silica particles to create geometrically well-defined colloidal (nano) clusters. PMID:25127340

  13. Tropospheric Chemistry

    NASA Technical Reports Server (NTRS)

    Mohnen, V.

    1984-01-01

    The fundamental processes that control the chemical composition and cycles of the global troposphere and how these processes and properties affect the physical behavior of the atmosphere are examined. The long-term information needs for tropospheric chemistry are: to be able to predict tropospheric responses to perturbations, both natural and anthropogenic, of these cycles, and to provide the information required for the maintenance and effective future management of the atmospheric component of our global life support system. The processes controlling global tropospheric biogeochemical cycles include: the input of trace species into the troposphere, their long-range transport and distribution as affected by the mean wind and vertical venting, their chemical transformations, including gas to particle conversion, leading to the appearance of aerosols or aqueous phase reactions inside cloud droplets, and their removal from the troposphere via wet (precipitation) and dry deposition.

  14. Combustion chemistry

    SciTech Connect

    Brown, N.J.

    1993-12-01

    This research is concerned with the development and use of sensitivity analysis tools to probe the response of dependent variables to model input variables. Sensitivity analysis is important at all levels of combustion modeling. This group`s research continues to be focused on elucidating the interrelationship between features in the underlying potential energy surface (obtained from ab initio quantum chemistry calculations) and their responses in the quantum dynamics, e.g., reactive transition probabilities, cross sections, and thermal rate coefficients. The goals of this research are: (i) to provide feedback information to quantum chemists in their potential surface refinement efforts, and (ii) to gain a better understanding of how various regions in the potential influence the dynamics. These investigations are carried out with the methodology of quantum functional sensitivity analysis (QFSA).

  15. Specific activity of polypyrrole nanoparticulate immunoreagents: comparison of surface chemistry and immobilization options.

    PubMed

    Pope, M R; Armes, S P; Tarcha, P J

    1996-01-01

    Polypyrrole-based colloids with differing surface chemistries were compared with respect to the specific activity of immobilized antibody. Monoclonal antibody to the alpha subunit of human chorionic gonadotropin (hCG) was modified by incorporation of cystamine into the Fc-carbohydrate, followed by reduction with dithiothreitol resulting in the generation of 4.5 free thiols per IgG. The reduced IgG was added to clean, unmodified and surface-modified polypyrrole colloids. Functionalized colloids included carboxylate-modified polypyrrole, poly[pyrrole-co-1-(2-carboxyethyl) pyrrole]-silica composite, and amine forms of the carboxylated colloids. The amine-functionalized colloids were subsequently treated with sulfosuccinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate to provide thiol-reactive maleimide surface groups. Following the conjugation of IgG to the colloids, bound and soluble antibody activity was quantitated using a sequentially competitive immunoassay for hCG, based on an automated commercial hCG kit. The results indicated that all forms of polypyrrole retained the equivalence of between 12 and 33 micrograms of IgG activity/mg of colloidal solids, relative to the unmodified soluble IgG. PMID:8853457

  16. Influence of heteroaggregation processes between intrinsic colloids and carrier colloids on cerium(III) mobility through fractured carbonate rocks.

    PubMed

    Tran, Emily; Klein Ben-David, Ofra; Teutch, Nadya; Weisbrod, Noam

    2016-09-01

    Colloid facilitated transport of radionuclides has been implicated as a major transport vector for leaked nuclear waste in the subsurface. Sorption of radionuclides onto mobile carrier colloids such as bentonite and humic acid often accelerates their transport through saturated rock fractures. Here, we employ column studies to investigate the impact of intrinsic, bentonite and humic acid colloids on the transport and recovery of Ce(III) through a fractured chalk core. Ce(III) recovery where either bentonite or humic colloids were added was 7.7-26.9% Ce for all experiments. Greater Ce(III) recovery was observed when both types of carrier colloids were present (25.4-37.4%). When only bentonite colloids were present, Ce(III) appeared to be fractionated between chemical sorption to the bentonite colloid surfaces and heteroaggregation of bentonite colloids with intrinsic carbonate colloids, precipitated naturally in solution. However, scanning electron microscope (SEM) images and colloid stability experiments reveal that in suspensions of humic acid colloids, colloid-facilitated Ce(III) migration results only from the latter attachment mechanism rather than from chemical sorption. This observed heteroaggregation of different colloid types may be an important factor to consider when predicting potential mobility of leaked radionuclides from geological repositories for spent fuel located in carbonate rocks. PMID:27183207

  17. Technetium-99m antimony colloid for bone-marrow imaging

    SciTech Connect

    Martindale, A.A.; Papadimitriou, J.M.; Turner, J.H.

    1980-11-01

    Technetium-99m antimony colloid was prepared in our laboratory for bone-marrow imaging. Optimal production of colloid particles of size range 1 to 13 nm was achieved by the use of polyvinylpyrrolidone of mol. wt. 44,000. Electron microscopy was used to size the particles. Studies in rabbits showed exclusive concentration in the subendothelial dendritic phagocytes of the bone marrow. Pseudopods from these cells were found to traverse interendothelial junctions and concentrate colloid from the sinusoids. Imaging studies of bone marrow in rabbits showed the superiority of the Tc-99m antimony colloid over the much larger colloidal particle of Tc-99m sulfur colloid. Tissue distribution studies in the rat confirmed that bone-marrow uptake of Tc-99m antimony colloid was greater than that of Tc-99m sulfur colloid, although blood clearance was much slower.

  18. COLLOIDAL CONSIDERATIONS IN GROUNDWATER SAMPLING AND CONTAMINANT TRANSPORT PREDICTIONS

    EPA Science Inventory

    The association of contaminants with suspended colloidal material in groundwater is a possible transport mechanism and a complicating factor for accurate estimations of the aqueous geochemistry of subsurface systems. esearch to date indicates colloidal facilitated transport of co...

  19. Industrial application of surface and colloid science

    SciTech Connect

    Borgarello, E.

    1995-12-01

    Interfacial phenomena are playing a key role in several industrial processes such as oil production and refining, synthesis of chemicals and catalytic reactions. Eniricerche has gained a quite wide experience in applied colloid science in the last fifteen years working together with the Operating Companies of the ENI group. The main areas of interest have been oil production and transportation, fuel formulation, lubrication, bitumen, detergency, reactions in microemulsions, gels for cosmetics, blood substitutes, and photocatalytic degradation of pollutants in colloidal dispersions. The understanding of the interfacial phenomena occurring at the solid-liquid or at the liquid-liquid interface has been a major contribution to the solution of industrial problems. After a short description of Eniricerche activities in applied colloid science, two examples will be described: the hydroformulation of olefines in a microemulsion and the transportation of heavy oil in an oil-in-water emulsion.

  20. Nematic colloidal tilings as photonic materials

    NASA Astrophysics Data System (ADS)

    Ravnik, M.; Dontabhaktuni, J.; Cancula, M.; Zumer, S.

    2014-02-01

    Colloidal platelets are explored as elementary building blocks for the shape-controlled assembly of crystalline and quasicrystalline tilings. Using three-dimensional (3D) numerical modelling based on the minimization of Landau-de Gennes free energy for modelling of colloids combined with Finite Difference Time Domain calculations for optics, we demonstrate the self-assembly and optical (transmission) properties of triangular, square and pentagonal sub-micrometer sized platelets in a thin layer of nematic liquid crystal. Interactions between platelets are explored, providing an insight into the assembly process. Two-dimensional tilings of various-shaped colloidal platelets are demonstrated, and their use as diffraction layers is explored by using FDTD simulations. Designing symmetry-breaking surface anchoring profiles on pentagonal platelets opens also a possibility to achieve interactions that could lead to tilings with non-crystalline symmetry.

  1. Shape-shifting colloids via stimulated dewetting

    NASA Astrophysics Data System (ADS)

    Youssef, Mena; Hueckel, Theodore; Yi, Gi-Ra; Sacanna, Stefano

    2016-07-01

    The ability to reconfigure elementary building blocks from one structure to another is key to many biological systems. Bringing the intrinsic adaptability of biological systems to traditional synthetic materials is currently one of the biggest scientific challenges in material engineering. Here we introduce a new design concept for the experimental realization of self-assembling systems with built-in shape-shifting elements. We demonstrate that dewetting forces between an oil phase and solid colloidal substrates can be exploited to engineer shape-shifting particles whose geometry can be changed on demand by a chemical or optical signal. We find this approach to be quite general and applicable to a broad spectrum of materials, including polymers, semiconductors and magnetic materials. This synthetic methodology can be further adopted as a new experimental platform for designing and rapidly prototyping functional colloids, such as reconfigurable micro swimmers, colloidal surfactants and switchable building blocks for self-assembly.

  2. Colloids in food: ingredients, structure, and stability.

    PubMed

    Dickinson, Eric

    2015-01-01

    This article reviews progress in the field of food colloids with particular emphasis on advances in novel functional ingredients and nanoscale structuring. Specific aspects of ingredient development described here are the stabilization of bubbles and foams by the protein hydrophobin, the emulsifying characteristics of Maillard-type protein-polysaccharide conjugates, the structural and functional properties of protein fibrils, and the Pickering stabilization of dispersed droplets by food-grade nanoparticles and microparticles. Building on advances in the nanoscience of biological materials, the application of structural design principles to the fabrication of edible colloids is leading to progress in the fabrication of functional dispersed systems-multilayer interfaces, multiple emulsions, and gel-like emulsions. The associated physicochemical insight is contributing to our mechanistic understanding of oral processing and textural perception of food systems and to the development of colloid-based strategies to control delivery of nutrients during food digestion within the human gastrointestinal tract. PMID:25422877

  3. Dynamic Assembly of Magnetic Colloidal Vortices.

    PubMed

    Mohorič, Tomaž; Kokot, Gašper; Osterman, Natan; Snezhko, Alexey; Vilfan, Andrej; Babič, Dušan; Dobnikar, Jure

    2016-05-24

    Magnetic colloids in external time-dependent fields are subject to complex induced many-body interactions governing their self-assembly into a variety of equilibrium and out-of-equilibrium structures such as chains, networks, suspended membranes, and colloidal foams. Here, we report experiments, simulations, and theory probing the dynamic assembly of superparamagnetic colloids in precessing external magnetic fields. Within a range of field frequencies, we observe dynamic large-scale structures such as ordered phases composed of precessing chains, ribbons, and rotating fluidic vortices. We show that the structure formation is inherently coupled to the buildup of torque, which originates from internal relaxation of induced dipoles and from transient correlations among the particles as a result of short-lived chain formation. We discuss in detail the physical properties of the vortex phase and demonstrate its potential in particle-coating applications. PMID:27128501

  4. Collective behavior of thermally active colloids.

    PubMed

    Golestanian, Ramin

    2012-01-20

    Colloids with patchy metal coating under laser irradiation could act as local heat sources and generate temperature gradients that could induce self-propulsion and interactions between them. The collective behavior of a dilute solution of such thermally active particles is studied using a stochastic formulation. It is found that when the Soret coefficient is positive, the system could be described in a stationary state by the nonlinear Poisson-Boltzmann equation and could adopt density profiles with significant depletion in the middle region when confined. For colloids with a negative Soret coefficient, the system can be described as a dissipative equivalent of a gravitational system. It is shown that in this case the thermally active colloidal solution could undergo an instability at a critical laser intensity, which has similarities to a supernova explosion. PMID:22400792

  5. Collective Behavior of Thermally Active Colloids

    NASA Astrophysics Data System (ADS)

    Golestanian, Ramin

    2012-01-01

    Colloids with patchy metal coating under laser irradiation could act as local heat sources and generate temperature gradients that could induce self-propulsion and interactions between them. The collective behavior of a dilute solution of such thermally active particles is studied using a stochastic formulation. It is found that when the Soret coefficient is positive, the system could be described in a stationary state by the nonlinear Poisson-Boltzmann equation and could adopt density profiles with significant depletion in the middle region when confined. For colloids with a negative Soret coefficient, the system can be described as a dissipative equivalent of a gravitational system. It is shown that in this case the thermally active colloidal solution could undergo an instability at a critical laser intensity, which has similarities to a supernova explosion.

  6. Boundaries Matter for Confined Colloidal Glasses

    NASA Astrophysics Data System (ADS)

    Hunter, Gary L.; Edmond, Kazem V.; Weeks, Eric R.

    2012-02-01

    We confine dense colloidal suspensions within emulsion droplets to examine how confinement and properties of the confining medium affect the colloidal glass transition. Samples are imaged via fast confocal microscopy. By observing a wide range of droplet sizes and varying the viscosity of the external continuous phase, we separate finite size and boundary effects on particle motions within the droplet. Suspensions are composed of binary PMMA spheres in organic solvents while the external phases are simple mixtures of water and glycerol. In analogy with molecular super-cooled liquids and thin-film polymers, we find that confinement effects in colloidal systems are not merely functions of the finite size of the system, but are strongly dependent on the viscosity of the confining medium and interactions between particles and the interface of the two phases.

  7. Shape-shifting colloids via stimulated dewetting.

    PubMed

    Youssef, Mena; Hueckel, Theodore; Yi, Gi-Ra; Sacanna, Stefano

    2016-01-01

    The ability to reconfigure elementary building blocks from one structure to another is key to many biological systems. Bringing the intrinsic adaptability of biological systems to traditional synthetic materials is currently one of the biggest scientific challenges in material engineering. Here we introduce a new design concept for the experimental realization of self-assembling systems with built-in shape-shifting elements. We demonstrate that dewetting forces between an oil phase and solid colloidal substrates can be exploited to engineer shape-shifting particles whose geometry can be changed on demand by a chemical or optical signal. We find this approach to be quite general and applicable to a broad spectrum of materials, including polymers, semiconductors and magnetic materials. This synthetic methodology can be further adopted as a new experimental platform for designing and rapidly prototyping functional colloids, such as reconfigurable micro swimmers, colloidal surfactants and switchable building blocks for self-assembly. PMID:27426418

  8. Convection of a stratified colloidal suspension

    SciTech Connect

    Cherepanov, I. N.; Smorodin, B. L.

    2013-11-15

    The convection of a colloidal suspension, which is a binary mixture of a carrier medium with an admixture of nanoparticles having a large positive thermal diffusion parameter, has been studied for the case of the heating of a horizontal cell from below and periodic conditions at the vertical boundaries corresponding to the experimental situation of ring channels. Bifurcation diagrams have been constructed for vibrational and monotonic regimes of the convection of the colloidal mixture. The time dependences of the maximum stream function and the stream function at a fixed point of the cell, as well as the spatial distributions of the concentration field of the colloid admixture, have been obtained. It has been shown that a stable regime of traveling waves exists in a certain region of the parameters of the problem (Boltzmann and Rayleigh numbers characterizing the gravitational stratification and intensity of the thermal effect, respectively)

  9. Premelting at Defects Within Bulk Colloidal Crystals

    NASA Astrophysics Data System (ADS)

    Alsayed, A. M.; Islam, M. F.; Zhang, J.; Collings, P. J.; Yodh, A. G.

    2005-08-01

    Premelting is the localized loss of crystalline order at surfaces and defects at temperatures below the bulk melting transition. It can be thought of as the nucleation of the melting process. Premelting has been observed at the surfaces of crystals but not within. We report observations of premelting at grain boundaries and dislocations within bulk colloidal crystals using real-time video microscopy. The crystals are equilibrium close-packed, three-dimensional colloidal structures made from thermally responsive microgel spheres. Particle tracking reveals increased disorder in crystalline regions bordering defects, the amount of which depends on the type of defect, distance from the defect, and particle volume fraction. Our observations suggest that interfacial free energy is the crucial parameter for premelting in colloidal and atomic-scale crystals.

  10. Targeted delivery of colloids by swimming bacteria

    PubMed Central

    Koumakis, N.; Lepore, A.; Maggi, C.; Di Leonardo, R.

    2013-01-01

    The possibility of exploiting motile microorganisms as tiny propellers represents a fascinating strategy for the transport of colloidal cargoes. However, delivery on target sites usually requires external control fields to steer propellers and trigger cargo release. The need for a constant feedback mechanism prevents the design of compact devices where biopropellers could perform their tasks autonomously. Here we show that properly designed three-dimensional (3D) microstructures can define accumulation areas where bacteria spontaneously and efficiently store colloidal beads. The process is stochastic in nature and results from the rectifying action of an asymmetric energy landscape over the fluctuating forces arising from collisions with swimming bacteria. As a result, the concentration of colloids over target areas can be strongly increased or depleted according to the topography of the underlying structures. Besides the significance to technological applications, our experiments pose some important questions regarding the structure of stationary probability distributions in non-equilibrium systems. PMID:24100868

  11. Shape-shifting colloids via stimulated dewetting

    PubMed Central

    Youssef, Mena; Hueckel, Theodore; Yi, Gi-Ra; Sacanna, Stefano

    2016-01-01

    The ability to reconfigure elementary building blocks from one structure to another is key to many biological systems. Bringing the intrinsic adaptability of biological systems to traditional synthetic materials is currently one of the biggest scientific challenges in material engineering. Here we introduce a new design concept for the experimental realization of self-assembling systems with built-in shape-shifting elements. We demonstrate that dewetting forces between an oil phase and solid colloidal substrates can be exploited to engineer shape-shifting particles whose geometry can be changed on demand by a chemical or optical signal. We find this approach to be quite general and applicable to a broad spectrum of materials, including polymers, semiconductors and magnetic materials. This synthetic methodology can be further adopted as a new experimental platform for designing and rapidly prototyping functional colloids, such as reconfigurable micro swimmers, colloidal surfactants and switchable building blocks for self-assembly. PMID:27426418

  12. Colloidal Disorder-Order Transition (CDOT-2)

    NASA Technical Reports Server (NTRS)

    2004-01-01

    This is an image of a colloidal crystal from the CDOT-2 investigation flown on STS-95. There are so many colloidal particles in this sample that it behaves like a glass. In the laboratory on Earth, the sample remained in an amorphous state, showing no sign of crystal growth. In microgravity the sample crystallized in 3 days, as did the other glassy colloidal samples examined in the CDOT-2 experiment. During the investigation, crystallization occurred in samples that had a volume fraction (number of particles per total volume) larger than the formerly reported glass transition of 0.58. This has great implications for theories of the structural glass transition. These crystals were strong enough to survive space shuttle re-entry and landing.

  13. Phosphate binding by natural iron-rich colloids in streams.

    PubMed

    Baken, Stijn; Moens, Claudia; van der Grift, Bas; Smolders, Erik

    2016-07-01

    Phosphorus (P) in natural waters may be bound to iron (Fe) bearing colloids. However, the natural variation in composition and P binding strength of these colloids remain unclear. We related the composition of "coarse colloids" (colloids in the 0.1-1.2 μm size range) in 47 Belgian streams to the chemical properties of the streamwater. On average, 29% of the P in filtered (<1.2 μm) samples of these streams is present in coarse colloids. The concentration of Fe-rich colloids in streams decreases with increasing water hardness and pH. The P bearing colloids in these streams mostly consist of Fe hydroxyphosphates and of Fe oxyhydroxides with surface adsorbed P, which is underpinned by geochemical speciation calculations. In waters with molar P:Fe ratios above 0.5, only a minor part of the P is bound to coarse colloids. In such waters, the colloids have molar P:Fe ratios between 0.2 and 1 and are, therefore, nearly saturated with P. Conversely, in streams with molar P:Fe ratios below 0.1, most of the P is bound to Fe-rich colloids. Equilibration of synthetic and natural Fe and P bearing colloids with a zero sink reveals that colloids with low molar P:Fe ratios contain mostly nonlabile P, whereas P-saturated colloids contain mostly labile P which can be released within 7 days. Equilibration at a fixed free orthophosphate activity shows that the Fe-rich colloids may bind only limited P through surface adsorption, in the range of 0.02-0.04 mol P (mol Fe)(-1). The P:Fe ratios measured in naturally occurring Fe and P bearing colloids is clearly higher (between 0.05 and 1). These colloids are therefore likely formed by coprecipitation of P during oxidation of Fe(II), which leads to the formation of Fe hydroxyphosphate minerals. PMID:27110889

  14. Why Teach Environmental Chemistry?

    ERIC Educational Resources Information Center

    Gardner, Marjorie H.

    1974-01-01

    Discusses the importance of teaching environmental chemistry in secondary school science classes, and outlines five examples of environmental chemistry problems that focus on major concepts of chemistry and have critical implications for human survival and well-being. (JR)

  15. Science Update: Inorganic Chemistry

    ERIC Educational Resources Information Center

    Rawls, Rebecca

    1978-01-01

    This first in a series of articles describing the state of the art of various branches of chemistry reviews inorganic chemistry, including bioinorganic, photochemistry, organometallic, and solid state chemistries. (SL)

  16. Colloidal-gold electrosensor measuring device

    DOEpatents

    Wegner, Steven; Harpold, Michael A.; McCaffrey, Terence M.; Morris, Susan E.; Wojciechowski, Marek; Zhao, Junguo; Henkens, Robert W.; Naser, Najih; O'Daly, John P.

    1995-01-01

    The present invention provides a new device for use in measuring lead levels in biological and environmental samples. Using square wave coulometry and colloidal gold particles impregnated on carbon electrodes, the present invention provides a rapid, reliable, portable and inexpensive means of detecting low lead levels. The colloidal gold modified electrodes have microelectrode array characteristics and produce significantly higher stripping detection signals for lead than are produced at bulk gold electrode surfaces. The method is effective in determining levels of lead down to at least 5 .mu.g/dL in blood samples as small as 10 .mu.L.

  17. Dynamic Light Scattering From Colloidal Gels

    NASA Technical Reports Server (NTRS)

    Krall, A. H.; Weitz, David A.

    1996-01-01

    We present a brief, preliminary account of the interpretation of dynamic light scattering from fractal colloidal gels. For small scattering angles, and for high initial colloid particle volume fractions, the correlation functions exhibit arrested decay, reflecting the non-ergodic nature of these systems and allowing us to directly determine the elastic modulus of the gels. For smaller initial volume fractions, the correlation functions decay completely. In all cases, the initial decay is not exponential, but is instead described by a stretched exponential. We summarize the principles of a model that accounts for these data and discuss the scaling behavior of the measured parameters.

  18. Wetting reversal in colloid-polymer systems.

    PubMed

    Blokhuis, Edgar M; Kuipers, Joris

    2010-05-01

    The wetting of a phase-separated colloid-polymer mixture in contact with a hard wall is analyzed using free volume theory in a Nakanishi-Fisher-type approach. We present results for the wetting phase diagram for several model approximations. Our analysis is compared with a previous analysis by Aarts [J. Chem. Phys. 120, 1973 (2004)]. We find that there is a crossover from wetting to drying at a threshold value for the colloid-polymer size ratio and that the transitions are close to the critical point and of second order in nature. PMID:20866234

  19. Fabrication of anisotropic multifunctional colloidal carriers

    NASA Astrophysics Data System (ADS)

    Jerri, Huda A.

    The field of colloidal assembly has grown tremendously in recent years, although the direct or template-assisted methods used to fabricate complex colloidal constructions from monodisperse micro- and nanoparticles have been generally demonstrated on model materials. In this work, novel core particle syntheses, particle functionalizations and bottom-up assembly techniques are presented to create functional colloidal devices. Using particle lithography, high-information colloidal vectors have been developed and modified with imaging and targeting agents. Localized nanoscale patches have been reliably positioned on microparticles to serve as foundations for further chemical or physical modifications. Site-specific placement of RGD targeting ligands has been achieved in these lithographed patches. Preferential uptake of these targeted vectors by RGD-specific 3T3 fibroblasts was verified using confocal laser scanning microscopy. A transition was made from the functionalization of model imaging core particles to the lithography of colloidal cartridges, in an effort to construct colloidal syringes with specialized, programmable release profiles. A variety of functional, pH-sensitive fluorescent cores were engineered to respond to solution conditions. When triggered, the diverse composite core microparticles and reservoir microcapsules released embedded fluorescent moieties such as dye molecules, and fluorophore-conjugated nanoparticles. The microcapsules, created using layer-by-layer polyelectrolyte deposition on sacrificial templates, were selectively modified with a robust coating. The pH-responsive anisotropic reservoir microcapsules were extremely stable in solution, and exhibited a "Lazarus" functionality of rehydrating to their original state following desiccation. A snapshot of focused-release of core constituents through the lone opening in colloidal monotremes has been obtained by anisotropically-functionalizing degradable cores with barrier shells. Additionally

  20. Synthesis of Ionic Colloidal Crystals (ICCs)

    NASA Astrophysics Data System (ADS)

    Maskaly, Garry R.; Garcia, R. Edwin; Carter, W. Craig; Chiang, Yet-Ming

    2003-03-01

    Binary ionic colloidal crystals (ICCs) have been produced by ordered heterocoagulation of colloidal mixtures of silica (negative surface charge) and polystyrene functionalized with amidine (positive surface charge) suspended in isopropanol. Experimental conditions predicted by the theoretical model discussed in a separate talk have been implemented to obtain heterocoagulation of these particles in the rocksalt structure. To our knowledge, this is the first experimental demonstration of the ICC concept. The importance of various experimental parameters on ICC formation is discussed. Particle dynamics simulations are carried out to provide insight into the kinetics of ICCs. Potential applications are discussed.

  1. Colloidal-gold electrosensor measuring device

    DOEpatents

    Wegner, S.; Harpold, M.A.; McCaffrey, T.M.; Morris, S.E.; Wojciechowski, M.; Zhao, J.; Henkens, R.W.; Naser, N.; O`Daly, J.P.

    1995-11-21

    The present invention provides a new device for use in measuring lead levels in biological and environmental samples. Using square wave coulometry and colloidal gold particles impregnated on carbon electrodes, the present invention provides a rapid, reliable, portable and inexpensive means of detecting low lead levels. The colloidal gold modified electrodes have microelectrode array characteristics and produce significantly higher stripping detection signals for lead than are produced at bulk gold electrode surfaces. The method is effective in determining levels of lead down to at least 5 {micro}g/dL in blood samples as small as 10 {micro}L. 9 figs.

  2. Controlling colloidal interaction through asymetric functionalization

    NASA Astrophysics Data System (ADS)

    Snyder, Charles E.

    The use of colloids and nanoparticles is becoming more and more prevalent across all scientific disciplines. The ability to control how these particles interact may yield new structures with unique and useful properties. This thesis contributes a new method of creating dual functionality on colloids, "particle lithography". These modified colloids may be used to bottom-up assemble asymmetric colloidal aggregate structures. Particle lithography allows for the site specific functionalization of a colloid at a single site. The technique is not limited to any specific material and is scalable. The ability to control the patch's size is demonstrated. Characterization of the patch confirms the ability to control the patch size through varying the size of the colloid, the hydrodynamic radius of the coating particles or molecules, and the salt concentration at which the coating is applied. The effects of other experimental conditions on the particle lithography process, such as sonication, are examined. The particle lithography process is extended to functionalize a colloid at two sites. The sites are ninety degrees relative to the center of the colloid. This functionalization is used to form self-assembled trimers. Through this process, the ability to use other particles as masking agents in the particle lithography process is demonstrated. Also demonstrated is the ability to assemble particles composed of differing materials. Modeling aided in understanding how a lithographed and complementary particle might interact. Phase diagrams were constructed to show the critical coagulation concentration of salt needed for a lithographed particle to bind to its complement. This salt concentration is a function of patch size and potential, and particle size and potential. An effective patch size is defined and found to vary little as a function of system parameters. Defining a critical coagulation concentration suggests the ability to store lithographed precursor particles. This

  3. Dynamics of Colloidal Disorder-Order Transition

    NASA Technical Reports Server (NTRS)

    2001-01-01

    Experiments with colloidal solutions of plastic microspheres suspended in a liquid serve as models of how molecules interact and form crystals. For the Dynamics of Colloidal Disorder-Order Transition (CDOT) experiment, Paul Chaikin of Princeton University has identified effects that are attributable to Earth's gravity and demonstrated that experiments are needed in the microgravity of orbit. Space experiments have produced unexpected dendritic (snowflake-like) structures. To date, the largest hard sphere crystal grown is a 3 mm single crystal grown at the cool end of a ground sample. At least two more additional flight experiments are plarned aboard the International Space Station. This image is from a video downlink.

  4. Partial rejuvenation of a colloidal glass.

    PubMed

    Ozon, F; Narita, T; Knaebel, A; Debrégeas, G; Hébraud, P; Munch, J-P

    2003-09-01

    We study the effect of shear on the aging dynamics of a colloidal suspension of synthetic clay particles. We find that a shear of amplitude gamma reduces the relaxation time measured just after the cessation of shear by a factor exp(-gamma/gamma(c)), with gamma(c) approximately 5%, and is independent of the duration and the frequency of the shear. This simple law for the rejuvenation effect shows that the energy involved in colloidal rearrangements is proportional to the shear amplitude gamma rather than gamma(2), leading to an Eyring-like description of the dynamics of our system. PMID:14524814

  5. Bidisperse colloids: nanoparticles and microemulsions in coexistence.

    PubMed

    Tabor, Rico F; Eastoe, Julian; Dowding, Peter J; Grillo, Isabelle; Rogers, Sarah E

    2010-04-15

    Mixed 'hard-soft' colloidal systems have been generated in which the 'hard' components (80 nm diameter silica nanoparticles) coexist with a population of 'soft' microemulsion droplets, both structures stabilised by the anionic surfactant sodium bis(ethylhexyl)sulfosuccinate (AOT) with toluene as solvent. The addition of water to swell the inverse micelles to form microemulsion droplets appears to increase attractive interactions between the silica particles (determined by DLS), possibly due to adsorption of some water at the silica-toluene interface; however, long-term stability of the dispersions is maintained. Small-angle neutron scattering was used to examine the structures present in these new colloidal systems. PMID:20144832

  6. Binary Colloidal Alloy Test-5: Compete

    NASA Technical Reports Server (NTRS)

    Frisken, Barbara J.; Bailey, Arthur E.; Weitz, David A.

    2008-01-01

    The Binary Colloidal Alloy Test - 5: Compete (BCAT-5-Compete) investigation will photograph andomized colloidal samples onboard the International Space Station (ISS) to determine their resulting structure over time. The use of EarthKAM software and hardware will allow the scientists to capture the kinetics (evolution) of their samples, as well as the final equilibrium state of each sample. BCAT-5-Compete will utilize samples 6 - 8 in the BCAT-5 hardware to study the competition between phase separation and crystallization, which is important in the manufacture of plastics and other materials.

  7. Self-assembly of colloidal surfactants

    NASA Astrophysics Data System (ADS)

    Kegel, Willem

    2012-02-01

    We developed colloidal dumbbells with a rough and a smooth part, based on a method reported in Ref. [1]. Specific attraction between the smooth parts occurs upon addition of non-adsorbing polymers of appropriate size. We present the first results in terms of the assemblies that emerge in these systems. [4pt] [1] D.J. Kraft, W.S. Vlug, C.M. van Kats, A. van Blaaderen, A. Imhof and W.K. Kegel, Self-assembly of colloids with liquid protrusions, J. Am. Chem. Soc. 131, 1182, (2009)

  8. Collective sliding states for colloidal molecular crystals

    SciTech Connect

    Reichhardt, Charles; Reichhardt, Cynthia

    2008-01-01

    We study the driving of colloidal molecular crystals over periodic substrates such as those created with optical traps. The n-merization that occurs in the colloidal molecular crystal states produces a remarkably rich variety of distinct dynamical behaviors, including polarization effects within the pinned phase and the formation of both ordered and disordered sliding phases. Using computer simulations, we map the dynamic phase diagrams as a function of substrate strength for dimers and trimers on a triangular substrate, and correlate features on the phase diagram with transport signatures.

  9. Binary Colloidal Alloy Test-5: Phase Separation

    NASA Technical Reports Server (NTRS)

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

    2008-01-01

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

  10. Colloid mobilization and transport during capillary fringe fluctuations.

    PubMed

    Aramrak, Surachet; Flury, Markus; Harsh, James B; Zollars, Richard L

    2014-07-01

    Capillary fringe fluctuations due to changing water tables lead to displacement of air-water interfaces in soils and sediments. These moving air-water interfaces can mobilize colloids. We visualized colloids interacting with moving air-water interfaces during capillary fringe fluctuations by confocal microscopy. We simulated capillary fringe fluctuations in a glass-bead-filled column. We studied four specific conditions: (1) colloids suspended in the aqueous phase, (2) colloids attached to the glass beads in an initially wet porous medium, (3) colloids attached to the glass beads in an initially dry porous medium, and (4) colloids suspended in the aqueous phase with the presence of a static air bubble. Confocal images confirmed that the capillary fringe fluctuations affect colloid transport behavior. Hydrophilic negatively charged colloids initially suspended in the aqueous phase were deposited at the solid-water interface after a drainage passage, but then were removed by subsequent capillary fringe fluctuations. The colloids that were initially attached to the wet or dry glass bead surface were detached by moving air-water interfaces in the capillary fringe. Hydrophilic negatively charged colloids did not attach to static air-bubbles, but hydrophobic negatively charged and hydrophilic positively charged colloids did. Our results demonstrate that capillary fringe fluctuations are an effective means for colloid mobilization. PMID:24897130

  11. Fabrication of High Sensitive Immunochromato Kit Using Au Colloid

    NASA Astrophysics Data System (ADS)

    Okamoto, Koji

    Au colloid have characteristics of surface plasmon resonance with absorption at 500 nm~600 nm wavelength. Surface on the citric acid Au colloid can be conjugated with protein eg. antibody. Various particle size of Au colloid makes it high sensitive immunochromato as diagnostics. High sensitive immunochromato will be useful for application of cancer marker eg. prostate specific antigen and influenza early diagnosis.

  12. Ultrasound Propagation in Colloidal Dispersions.

    NASA Astrophysics Data System (ADS)

    Sherman, Nigel E.

    Available from UMI in association with The British Library. This thesis describes apparatus and techniques for making ultrasonic measurements in fluids and applications of them to measurements of ultrasonic parameters in colloidal dispersions. A brief description of the properties and uses of ultrasound propagation in dispersions is followed by an extensive review of theories which relate the particulate properties of the dispersions to the measurable ultrasonic parameters, velocity (c) and attenuation (alpha ). Measurement principles are outlined related to the design of near-field measurement methods and the development of three techniques is described. These are shown to give results which are both highly self-consistent and in excellent agreement with a far-field method. Measurements of alpha and c for model dispersions of glass spheres in Newtonian liquids are shown to be in good agreement with the relevant theory when particle polydispersity is taken into account. For structured fluids as the continuous phase, the alpha and c data for suspensions of spheres are used to obtain the continuous phase viscosity ( eta). The alpha data agree approximately with the macroscopic viscosity, but the velocity data requires the introduction of a shear elastic term and the revision of theory in order to obtain agreement. Attenuation as a function of barite concentration in Newtonian liquids was investigated and the ultrasonic particle radius was found to be systematically larger than expected. This is attributed to particle rugosity. Measurements of alpha and c using non-gelling aqueous kaolinite suspensions are shown to agree well with theory when the eccentricity and the interactions of particles are taken into account. For gelling aqueous bentonite suspensions, alpha and c were found to be time-dependent over a period of several days following initial dispersion. The observed increases in both alpha and c are interpreted in terms of a growth in gel fraction and shear

  13. Colloids in the River Inn

    NASA Astrophysics Data System (ADS)

    Ueckert, Martina; Niessner, Reinhard; Baumann, Thomas

    2015-04-01

    In the light of an increasing number of technical applications using nanoparticles and reports of adverse effects of engineered nanoparticles, research on the occurrence and stability of particles in all compartments has to be intensified. Colloids in river water represent the geologic setting, environmental conditions, and the anthropogenic use in its catchment. The river not only acts as a sink for nanoparticles but also as the source term due to exchange in the hyporheic zone and in bank filtration setups. The concentration, size distribution and elemental composition of particles in the River Inn were studied from the source in the Swiss Alps to the river mouth at Passau from 2008 to 2014. Samples were collected after each tributary from a sub-catchment and filtered on site using a new filtration device for gentle filtration. The elemental composition was determined after acid digestion with ICP/MS. SEM/EDX analysis provided morphological and elemental information for single particles. A complementary chemical analysis of the river water was performed to assess the geochemical stability of individual particles. As presented at EGU 2014, particles in the upper, rural parts mainly reveal changes in the geological setting of the tributary catchments. Not unexpectedly, particles originating from crystalline rocks, were more stable than particles originating from calcareous rocks. Anthropogenic and industrial influences increase in the lower parts. This went together with a change of the size distribution, an increase of the number of organic particles, and a decrease of the microfauna. Interestingly, specific leisure activities in a sub-catchment, like extensive downhill skiing, manifest itself in the particle composition. This general setting was validated in last year's sampling campaigns. An interesting change in on site parameters and hydrochemical composition was seen during all sampling campaigns at an inflow from the valley Kaunertal, Austria. Therefore

  14. Science Update: Inorganic Chemistry.

    ERIC Educational Resources Information Center

    Rawls, Rebecca

    1981-01-01

    Describes areas of inorganic chemistry which have changed dramatically in the past year or two, including photochemistry, electrochemistry, organometallic complexes, inorganic reaction theory, and solid state chemistry. (DS)

  15. Trace Chemistry

    NASA Technical Reports Server (NTRS)

    Radhakrishnan, Krishnan; Whitefield, Philip

    1999-01-01

    The goals of the trace chemistry group were to identify the processes relevant to aerosol and aerosol precursor formation occurring within aircraft gas turbine engines; that is, within the combustor, turbine, and nozzle. The topics of discussion focused on whether the chemistry of aerosol formation is homogeneous or heterogeneous; what species are important for aerosol and aerosol precursor formation; what modeling/theoretical activities to pursue; what experiments to carry out that both support modeling activities and elucidate fundamental processes; and the role of particulates in aerosol and aerosol precursor formation. The consensus of the group was that attention should be focused on SO2, SO3, and aerosols. Of immediate concern is the measurement of the concentration of the species SO3, SO2, H2SO4 OH, HO2, H2O2, O, NO, NO2, HONO, HNO3, CO, and CO2 and particulates in various engines, both those currently in use and those in development. The recommendation was that concentration measurements should be made at both the combustor exit and the engine exit. At each location the above species were classified into one of four categories of decreasing importance, Priority I through IV, as follows: Combustor exit: Priority I species - SO3:SO2 ratio, SO3, SO2, and particulates; Priority II species: OH and O; Priority III species - NO and NO2; and Priority IV species - CO and CO2. For the Engine exit: Priority I species - SO3:SO2 ratio, SO3, SO2,H2SO4, and particulates; Priority II species: OH,HO2, H2O2, and O; Priority III species - NO, NO2, HONO, and HNO3; and Priority IV species - CO and CO2. Table I summarizes the anticipated concentration range of each of these species. For particulate matter, the quantities of interest are the number density, size distribution, and composition. In order to provide data for validating multidimensional reacting flow models, it would be desirable to make 2-D, time-resolved measurements of the concentrations of the above species and

  16. Pore water colloid properties in argillaceous sedimentary rocks.

    PubMed

    Degueldre, Claude; Cloet, Veerle

    2016-11-01

    The focus of this work is to evaluate the colloid nature, concentration and size distribution in the pore water of Opalinus Clay and other sedimentary host rocks identified for a potential radioactive waste repository in Switzerland. Because colloids could not be measured in representative undisturbed porewater of these host rocks, predictive modelling based on data from field and laboratory studies is applied. This approach allowed estimating the nature, concentration and size distributions of the colloids in the pore water of these host rocks. As a result of field campaigns, groundwater colloid concentrations are investigated on the basis of their size distribution quantified experimentally using single particle counting techniques. The colloid properties are estimated considering data gained from analogue hydrogeochemical systems ranging from mylonite features in crystalline fissures to sedimentary formations. The colloid concentrations were analysed as a function of the alkaline and alkaline earth element concentrations. Laboratory batch results on clay colloid generation from compacted pellets in quasi-stagnant water are also reported. Experiments with colloids in batch containers indicate that the size distribution of a colloidal suspension evolves toward a common particle size distribution independently of initial conditions. The final suspension size distribution was found to be a function of the attachment factor of the colloids. Finally, calculations were performed using a novel colloid distribution model based on colloid generation, aggregation and sedimentation rates to predict under in-situ conditions what makes colloid concentrations and size distributions batch- or fracture-size dependent. The data presented so far are compared with the field and laboratory data. The colloid occurrence, stability and mobility have been evaluated for the water of the considered potential host rocks. In the pore water of the considered sedimentary host rocks, the clay

  17. Prospects of Colloidal Copper Chalcogenide Nanocrystals.

    PubMed

    van der Stam, Ward; Berends, Anne C; de Mello Donega, Celso

    2016-03-01

    Over the past few years, colloidal copper chalcogenide nanocrystals (NCs) have emerged as promising alternatives to conventional Cd and Pb chalcogenide NCs. Owing to their wide size, shape, and composition tunability, Cu chalcogenide NCs hold great promise for several applications, such as photovoltaics, lighting and displays, and biomedical imaging. They also offer characteristics that are unparalleled by Cd and Pb chalcogenide NCs, such as plasmonic properties. Moreover, colloidal Cu chalcogenide NCs have low toxicity, potentially lower costs, and excellent colloidal stability. This makes them attractive materials for the large-scale deployment of inexpensive, sustainable, and environmentally benign solution-processed devices. Nevertheless, the synthesis of colloidal Cu chalcogenide NCs, especially that of ternary and quaternary compositions, has yet to reach the same level of mastery as that available for the prototypical Cd chalcogenide based NCs. This review provides a concise overview of this rapidly advancing field, sketching the state of the art and highlighting the key challenges. We discuss recent developments in the synthesis of size-, shape-, and composition-controlled NCs of Cu chalcogenides, with emphasis in strategies to circumvent the limitations arising from the need to precisely balance the reactivities of multiple precursors in synthesizing ternary and quaternary compositions. In this respect, we show that topotactic cation-exchange reactions are a promising alternative route to complex multinary Cu chalcogenide NCs and hetero-NCs, which are not attainable by conventional routes. The properties and potential applications of Cu chalcogenide NCs and hetero-NCs are also addressed. PMID:26684665

  18. Advanced Colloids Experiment (ACE-T1)

    NASA Technical Reports Server (NTRS)

    Meyer, William V.; Sicker, Ron; Brown, Dan; Eustace, John

    2015-01-01

    Increment 45 - 46 Science Symposium presentation of Advanced Colloids Experiment (ACE-T1) to RPO. The purpose of this event is for Principal Investigators to present their science objectives, testing approach, and measurement methods to agency scientists, managers, and other investigators.

  19. Colloid Formation at Waste Plume Fronts

    SciTech Connect

    Wan, Jiamin; Tokunaga, Tetsu K.; Saiz, Eduardo; Larsen, Joern T.; Zheng, Zuoping; Couture, Rex A.

    2004-05-22

    Highly saline and caustic tank waste solutions containing radionuclides and toxic metals have leaked into sediments at U. S. Department of Energy (DOE) facilities such as the Hanford Site (Washington State). Colloid transport is frequently invoked to explain migration of radionuclides and metals in the subsurface. To understand colloid formation during interactions between highly reactive fluids and sediments and its impact on contaminant transport, we simulated tank waste solution (TWS) leakage processes in laboratory columns at ambient and elevated (70 C) temperatures. We found that maximum formation of mobile colloids occurred at the plume fronts (hundreds to thousands times higher than within the plume bodies or during later leaching). Concentrations of suspended solids were as high as 3 mass%, and their particle-sizes ranged from tens of nm to a few {micro}m. Colloid chemical composition and mineralogy depended on temperature. During infiltration of the leaked high Na{sup +} waste solution, rapid and completed Na{sup +} replacement of exchangeable Ca{sup 2+} and Mg{sup 2+} from the sediment caused accumulation of these divalent cations at the moving plume front. Precipitation of supersaturated Ca{sup 2+}/Mg{sup 2+}-bearing minerals caused dramatic pH reduction at the plume front. In turn, the reduced pH caused precipitation of other minerals. This understanding can help predict the behavior of contaminant trace elements carried by the tank waste solutions, and could not have been obtained through conventional batch studies.

  20. Advanced Colloids Experiment (ACE-H-2)

    NASA Technical Reports Server (NTRS)

    Meyer, William V.; Sicker, Ron; Chmiel, Alan J.; Eustace, John; LaBarbera, Melissa

    2015-01-01

    Increment 43 - 44 Science Symposium presentation of Advanced Colloids Experiment (ACE-H-2) to RPO. The purpose of this event is for Principal Investigators to present their science objectives, testing approach, and measurement methods to agency scientists, managers, and other investigators.

  1. Colloidal crystal grain boundary formation and motion

    PubMed Central

    Edwards, Tara D.; Yang, Yuguang; Beltran-Villegas, Daniel J.; Bevan, Michael A.

    2014-01-01

    The ability to assemble nano- and micro- sized colloidal components into highly ordered configurations is often cited as the basis for developing advanced materials. However, the dynamics of stochastic grain boundary formation and motion have not been quantified, which limits the ability to control and anneal polycrystallinity in colloidal based materials. Here we use optical microscopy, Brownian Dynamic simulations, and a new dynamic analysis to study grain boundary motion in quasi-2D colloidal bicrystals formed within inhomogeneous AC electric fields. We introduce “low-dimensional” models using reaction coordinates for condensation and global order that capture first passage times between critical configurations at each applied voltage. The resulting models reveal that equal sized domains at a maximum misorientation angle show relaxation dominated by friction limited grain boundary diffusion; and in contrast, asymmetrically sized domains with less misorientation display much faster grain boundary migration due to significant thermodynamic driving forces. By quantifying such dynamics vs. compression (voltage), kinetic bottlenecks associated with slow grain boundary relaxation are understood, which can be used to guide the temporal assembly of defect-free single domain colloidal crystals. PMID:25139760

  2. Self assembly of anisotropic colloidal particles

    NASA Astrophysics Data System (ADS)

    Florea, Daniel; Wyss, Hans

    2012-02-01

    Colloidal particles have been successfully used as ''model atoms'', as their behavior can be more directly studied than that of atoms or molecules by direct imaging in a confocal microscope. Most studies have focussed on spherical particles with isotropic interactions. However, a range of interesting materials such as many supramolecular polymers or biopolymers exhibit highly directional interactions. To capture their behavior in colloidal model systems, particles with anisotropic interactions are clearly required. Here we use a colloidal system of nonspherical colloids, where highly directional interactions can be induced via depletion. By biaxially stretching spherical PMMA particles we create oblate spheroidal particles. We induce attractive interactions between these particles by adding a non-adsorbing polymer to the background liquid. The resulting depletion interaction is stronger along the minor axis of the oblate spheroids. We study the phase behavior of these materials as a function of the ellipsoid aspect ratio, the strength of the depletion interactions, and the particle concentration. The resulting morphologies are qualitatively different from those observed with spherical particles. This can be exploited for creating new materials with tailored structures.

  3. Photoelectrochromism in Tungsten Trioxide Colloidal Solutions

    ERIC Educational Resources Information Center

    Chenthamarakshan, C. R.; Tacconi, N. R. de; Xu, Lucy; Rajeshwar, Krishnan

    2004-01-01

    Photophysical and photochemical properties of semiconductor metal oxide colloids are studied in the context of photoelectrochemical conversion and storage of solar energy. The experiment teaches the instrumental principles of UV-visible spectrophotometry, spectral acquisition and background subtraction strategies and diode array spectrometers.

  4. Cobalt-doped cadmium selenide colloidal nanowires.

    PubMed

    Li, Zhen; Du, Ai Jun; Sun, Qiao; Aljada, Muhsen; Cheng, Li Na; Riley, Mark J; Zhu, Zhong Hua; Cheng, Zhen Xiang; Wang, Xiao Lin; Hall, Jeremy; Krausz, Elmars; Qiao, Shi Zhang; Smith, Sean C; Lu, Gao Qing Max

    2011-11-21

    Co(2+)-doped CdSe colloidal nanowires with tunable size and dopant concentration have been prepared by a solution-liquid-solid (SLS) approach for the first time. These doped nanowires exhibit anomalous photoluminescence temperature dependence in comparison with undoped nanowires. PMID:21975534

  5. Solid colloids with surface-mobile linkers.

    PubMed

    van der Meulen, Stef A J; Helms, Gesa; Dogterom, Marileen

    2015-06-17

    In this report we review the possibilities of using colloids with surface mobile linkers for the study of colloidal self-assembly processes. A promising route to create systems with mobile linkers is the use of lipid (bi-)layers. These lipid layers can be either used in the form of vesicles or as coatings for hard colloids and emulsion droplets. Inside the lipid bilayers molecules can be inserted via membrane anchors. Due to the fluidity of the lipid bilayer, the anchored molecules remain mobile. The use of different lipid mixtures even allows creating Janus-like particles that exhibit directional bonding if linkers are used which have a preference for a certain lipid phase. In nature mobile linkers can be found e.g. as receptors in cells. Therefore, towards the end of the review, we also briefly address the possibility of using colloids with surface mobile linkers as model systems to mimic cell-cell interactions and cell adhesion processes. PMID:25993272

  6. Motile Fluids: Granular, Colloidal and Living

    NASA Astrophysics Data System (ADS)

    Ramaswamy, Sriram

    2014-03-01

    My talk will present our recent results from theory, simulation and experiment on flocking, swarming and instabilities in diverse realizations of active systems. The findings I will report include: flocking at a distance in vibrated granular monolayers; the active hydrodynamics of self-propelled solids; clusters, asters and oscillations in colloidal chemotaxis. Supported by a J C Bose Fellowship.

  7. Collective dynamics of rotating colloidal particles

    NASA Astrophysics Data System (ADS)

    Magkiriadou, Sofia; Soni, Vishal; van Zuiden, Benny; Bartolo, Denis; Vitelli, Vincenzo; Irvine, William T. M.

    We study magnetic colloidal particles in suspension under the influence of a rotating magnetic field. When in aggregates, these particles show rich dynamics that are governed by magnetic and hydrodynamic interactions. By tuning these interactions, we probe the phase diagram of this system and study the emergent collective dynamics. Finally, we begin to investigate whether we can control this phase diagram with geometry.

  8. Grafting of oligosaccharides onto synthetic polymer colloids.

    PubMed

    Mange, Siyabonga; Dever, Cédric; De Bruyn, Hank; Gaborieau, Marianne; Castignolles, Patrice; Gilbert, Robert G

    2007-06-01

    A new method to form colloidally stable oligosaccharide-grafted synthetic polymer particles has been developed. The oligosaccharides, of weight-average degree of polymerization approximately 38, were obtained by enzymatic debranching of amylopectin. Through the use of a cerium(IV)-based redox initiation process, oligosaccharide chains are grafted onto a synthetic polymer colloid comprising electrostatically stabilized poly(methyl methacrylate) or polystyrene latex particles swollen with methyl methacrylate monomer. Ce(IV) creates a radical species on these oligosaccharides, which then propagates, initially with aqueous-phase monomer, then with the methyl methacrylate monomer inside the particles. Ultracentrifugation, NMR, and total starch analyses together prove that the grafting process has occurred, with at least 7.7 wt % starch grafted and a grafting efficiency of 33%. The surfactant used in latex preparation was removed by dialysis, resulting in particles colloidally stabilized with only linear starch as a steric stabilizer. The debranched starch that comprises these oligosaccharides is found to be a remarkably effective colloidal stabilizer, albeit at low electrolyte concentration, stabilizing particles with very sparse surface coverage. PMID:17497920

  9. Colloidal nickel boride catalyst for hydrogenation of olefins

    SciTech Connect

    Nakao, Y.; Fujishige, S.

    1981-04-01

    Colloidal nickel boride was prepared from nickel(II) chloride by reduction with sodium borohydride in the presence of polyvinylpyrrolidone in ethanol. Hydrogenation of various olefins was examined over the colloidal catalyst at 30/sup 0/C and atmospheric pressure. The colloidal nickel boride was much more effective than the precipitated nickel boride prepared in the absence of polyvinylpyrrolidone as a hydrogenation catalyst, especially for isopropenyl compounds. Additional amines and sodium acetate were slightly inhibitive to the colloidal catalyst, while, being strongly promotive to the precipitated catalyst. The colloidal nickel boride was superior to the charcoal-supported metals of the platinum group in catalytic activity for ..cap alpha..-methylstyrene.

  10. Bonded boojum-colloids in nematic liquid crystals.

    PubMed

    Eskandari, Zahra; Silvestre, Nuno M; Telo da Gama, Margarida M

    2013-08-20

    We investigate bonded boojum-colloids in nematic liquid crystals, configurations where two colloids with planar degenerate anchoring are double-bonded through line defects connecting their surfaces. This bonded structure promotes the formation of linear chains aligned with the nematic director. We show that the bonded configuration is the global minimum in systems that favor twist deformations. In addition, we investigate the influence of confinement on the stability of bonded boojum-colloids. Although the unbonded colloid configuration, where the colloids bundle at oblique angles, is favored by confinement, the bonded configuration is again the global minimum for liquid crystals with sufficiently small twist elastic constants. PMID:23859624

  11. Colloid suspension stability and transport through unsaturated porous media

    SciTech Connect

    McGraw, M.A.; Kaplan, D.I.

    1997-04-01

    Contaminant transport is traditionally modeled in a two-phase system: a mobile aqueous phase and an immobile solid phase. Over the last 15 years, there has been an increasing awareness of a third, mobile solid phase. This mobile solid phase, or mobile colloids, are organic or inorganic submicron-sized particles that move with groundwater flow. When colloids are present, the net effect on radionuclide transport is that radionuclides can move faster through the system. It is not known whether mobile colloids exist in the subsurface environment of the Hanford Site. Furthermore, it is not known if mobile colloids would likely exist in a plume emanating from a Low Level Waste (LLW) disposal site. No attempt was made in this study to ascertain whether colloids would form. Instead, experiments and calculations were conducted to evaluate the likelihood that colloids, if formed, would remain in suspension and move through saturated and unsaturated sediments. The objectives of this study were to evaluate three aspects of colloid-facilitated transport of radionuclides as they specifically relate to the LLW Performance Assessment. These objectives were: (1) determine if the chemical conditions likely to exist in the near and far field of the proposed disposal site are prone to induce flocculation (settling of colloids from suspension) or dispersion of naturally occurring Hanford colloids, (2) identify the important mechanisms likely involved in the removal of colloids from a Hanford sediment, and (3) determine if colloids can move through unsaturated porous media.

  12. Analysis of colloids released from bentonite and crushed rock

    NASA Astrophysics Data System (ADS)

    Lahtinen, M.; Hölttä, P.; Riekkola, M.-L.; Yohannes, G.

    Inorganic colloids are present in natural groundwater but colloids can also be produced from degraded Engineered Barrier System (EBS) materials. The potential relevance of colloids for radionuclide transport is highly dependent on the release and stability of colloids in different chemical environments and their interaction with radionuclides. In this work, release and stability of inorganic colloids were determined from bentonite and crushed rock which will be used in the tunnel back-fill. In the batch dispersion experiments, MX-80 bentonite powder or crushed rock samples of mica gneiss, unaltered and two altered tonalites were added to Milli-Q water, saline OLSO, and low salinity Allard reference water with adjusted pH values 7-9. After 4 months, pH, particle size distribution, zeta potential, morphology, elemental composition, and colloid concentration were analyzed. The release and stability of colloids depended significantly on groundwater salinity, pH, and the degree of alteration of the rock. In saline OLSO, zeta potential values near zero, wide particle size range, and low colloid concentrations indicated particle aggregation and instable colloidal dispersion. In low salinity Allard and Milli-Q water, high or moderate negative zeta potential values, smaller particle sizes, and higher colloid concentrations than in OLSO indicated the existence of stable colloids.

  13. Scattering from correlations in colloidal systems

    SciTech Connect

    Hayter, J.B.

    1984-01-01

    Colloidal suspensions typically exhibit spatial correlations over distances of order 10-10/sup 4/ A, corresponding either to the size of individual particles (e.g., polymer chains, surfactant micelles) or to the range of interaction between particles (e.g., charged polymer lattices at low ionic strength). Apart from having fundamental intrinsic interest, such systems are also extremely useful as model systems with which to study, for example, non-Newtonian hydrodynamics, since temporal correlations are generally much longer lived (10/sup -8/-10/sup -3/ sec) than those found in simple atomic or small molecular systems (10/sup -13/-10/sup -10/ sec). Colloids have long been the subject of macroscopic phenomenological research (on rheological properties, for example), but it is only recently that microscopic light, x-ray and neutron scattering techniques have been applied to their study, in large part because of theoretical difficulties in understanding the scattering from dense liquid-like systems of interacting particles. For spherical colloids, such theoretical problems have now been largely overcome, and for anisotropic colloids experimental techniques are being developed which circumvent the intractable theoretical areas. This paper will first review some static light and small-angle neutron scattering (SANS) results on colloidal suspensions, both at equilibrium and in steady-state non-equilibrium situations, and will then discuss some dynamic measurements on polymer solutions and melts made using the neutron spin-echo (NSE) technique. Emphasis is placed on experiments which have a possible counterpart in synchrotron radiation studies. In particular, NSE extends the results of photon correlation spectroscopy (PCS) to larger momentum transfers and shorter time-scales than are available with visible light, and the extension of PCS to short wavelength on a synchrotron source would be of similar fundamental interest.

  14. [Preliminary study of colloid osmotic pressure for cardiopulmonary bypass].

    PubMed

    Wang, D; Xiang, L; Luo, J

    1996-12-01

    The ideal colloid osmotic pressure is beneficial to decrease the fluid accumulated in the pulmonary and other tissue during cardiopulmonary bypass. Schupbach reported the proper colloidosmotic pressure for cardiopulmonary bypass was 2.1 kPa (16 mmHg). Colloid osmotic pressures of blood and priming fluid during cardiopulmonary bypass were measured in 28 patients with heart disease by using colloid osmotic pressure detection apparatus. The value of colloid osmotic pressure suitable for the designed standard was apparently different among the Gelofusine group and other groups. P value was 0.005. Priming fluid for cardiopulmonary bypass needs to satisfy the quality and the quantity of colloid osmotic pressure. Using Albumin isn't economical. Whole blood and plazma are not suitable for increasing colloid osmotic pressure. Hydroxyethyl starch or Gelofusine is best choice in priming to get designed standard of colloid osmotic pressure. The ratio of hydroxyethyl starch or Gelofusine in priming fluid should beyond 1/2. PMID:9590779

  15. Tracking liquid in drying colloidal fluids with polarized light microscopy

    NASA Astrophysics Data System (ADS)

    Cho, Kun; Park, Jung Soo; Kim, Joon Heon; Weon, Byung Mook

    2014-11-01

    When colloidal fluids dry, tracking liquid surfaces around colloids is difficult with conventional imaging techniques. Here we show that polarized light microscopy (PM) is very useful in tracking liquid surfaces during drying processes of colloidal fluids. In particular, the PM mode is not a new or difficult way but is able to visualize liquid films above colloids in real time. We demonstrate that when liquid films above colloidal particles are broken, the PM patterns appear clearly: this feature is useful to identify the moment of liquid film rupture above colloids in drying colloidal fluids. This result is helpful to improve relevant processes such as inkjet printing, painting, and nanoparticle patterning (K.C. and J.S.P. equally contributed). This work (NRF-2013R1A22A04008115) was supported by Mid-career Researcher Program through NRF grant funded by the MEST.

  16. Colloid Mobilization and Transport during Capillary Fringe Fluctuations

    NASA Astrophysics Data System (ADS)

    Aramrak, Surachet; Flury, Markus

    2016-04-01

    Capillary fringe fluctuations due to changing water tables lead to displacement of air-water interfaces in soils and sediments. These moving air-water interfaces can mobilize colloids. We visualized colloids interacting with moving air-water interfaces during capillary fringe fluctuations by confocal microscopy. We simulated capillary fringe fluctuations in a glass-bead filled column. Confocal images showed that the capillary fringe fluctuations affect colloid transport behavior. Hydrophilic negatively-charged colloids initially suspended in the aqueous phase were deposited at the solid-water interface after a drainage passage, but then were removed by subsequent capillary fringe fluctuations. The colloids that were initially attached to the wet or dry glass bead surface were detached by moving air-water interfaces in the capillary fringe. Hydrophilic negatively-charged colloids did not attach to static air-bubbles, but hydrophobic negatively-charged and hydrophilic positively-charged colloids did.

  17. Modeling of Hydrodynamic Chromatography for Colloid Migration in Fractured Rock

    SciTech Connect

    Li Shihhai; Jen, C.-P

    2001-02-15

    The role of colloids in the migration of radionuclides in the geosphere has been emphasized in the performance assessment of high-level radioactive waste disposal. The literature indicates that the colloid velocity may not be equal to the velocity of groundwater owing to hydrodynamic chromatography. A theoretical model for hydrodynamic chromatography of colloid migration in the fracture is proposed in the present work. In this model, the colloids are treated as nonreactive and the external forces acting on colloidal particles are considered including the inertial force, the van der Waals attractive force, and the electrical double-layer repulsive force, as well as the gravitational force. A fully developed concentration profile for colloids is obtained to elucidate migration behavior for colloids in the fracture. The effects of parameters governing these forces and the aperture of the fracture are determined using a theoretical model.

  18. Green synthesis of colloid silver nanoparticles and resulting biodegradable starch/silver nanocomposites.

    PubMed

    Cheviron, Perrine; Gouanvé, Fabrice; Espuche, Eliane

    2014-08-01

    Environmentally friendly silver nanocomposite films were prepared by an ex situ method consisting firstly in the preparation of colloidal silver dispersions and secondly in the dispersion of the as-prepared nanoparticles in a potato starch/glycerol matrix, keeping a green chemistry process all along the synthesis steps. In the first step concerned with the preparation of the colloidal silver dispersions, water, glucose and soluble starch were used as solvent, reducing agent and stabilizing agent, respectively. The influences of the glucose amount and reaction time were investigated on the size and size distribution of the silver nanoparticles. Two distinct silver nanoparticle populations in size (diameter around 5 nm size for the first one and from 20 to 50 nm for the second one) were distinguished and still highlighted in the potato starch/glycerol based nanocomposite films. It was remarkable that lower nanoparticle mean sizes were evidenced by both TEM and UV-vis analyses in the nanocomposites in comparison to the respective colloidal silver dispersions. A dispersion mechanism based on the potential interactions developed between the nanoparticles and the polymer matrix and on the polymer chain lengths was proposed to explain this morphology. These nanocomposite film series can be viewed as a promising candidate for many applications in antimicrobial packaging, biomedicines and sensors. PMID:24751276

  19. LONG-TERM COLLOID MOBILIZATION AND COLLOID-FACILITATED TRANSPORT OF RADIONUCLIDES IN A SEMI-ARID VADOSE ZONE

    SciTech Connect

    Markus Flury; James B. Harsh; Fred Zhang; Glendon W. Gee; Earl D. Mattson; Peter C. L

    2012-08-01

    The main purpose of this project was to improve the fundamental mechanistic understanding and quantification of long-term colloid mobilization and colloid-facilitated transport of radionuclides in the vadose zone, with special emphasis on the semi-arid Hanford site. While we focused some of the experiments on hydrogeological and geochemical conditions of the Hanford site, many of our results apply to colloid and colloid-facilitated transport in general. Specific objectives were (1) to determine the mechanisms of colloid mobilization and colloid-facilitated radionuclide transport in undisturbed Hanford sediments under unsaturated flow, (2) to quantify in situ colloid mobilization and colloid-facilitated radionuclidetransport from Hanford sediments under field conditions, and (3) to develop a field-scale conceptual and numerical model for colloid mobilization and transport at the Hanford vadose zone, and use that model to predict long-term colloid and colloid- facilitated radionuclide transport. To achieve these goals and objectives, we have used a combination of experimental, theoretical, and numerical methods at different spatial scales, ranging from microscopic investigationsof single particle attachment and detachment to larger-scale field experiments using outdoor lysimeters at the Hanford site. Microscopic and single particle investigations provided fundamental insight into mechanisms of colloid interactions with the air-water interface. We could show that a moving air water interface (such as a moving water front during infiltration and drainage) is very effective in removing and mobilizing particles from a stationary surface. We further demonstrated that it is particularly the advancing air-water interface which is mainly responsible for colloid mobilization. Forces acting on the colloids calculated from theory corroborated our experimental results, and confirm that the detachment forces (surface tension forces) during the advancing air-water interface

  20. Quantitative uptake of colloidal particles by cell cultures.

    PubMed

    Feliu, Neus; Hühn, Jonas; Zyuzin, Mikhail V; Ashraf, Sumaira; Valdeperez, Daniel; Masood, Atif; Said, Alaa Hassan; Escudero, Alberto; Pelaz, Beatriz; Gonzalez, Elena; Duarte, Miguel A Correa; Roy, Sathi; Chakraborty, Indranath; Lim, Mei L; Sjöqvist, Sebastian; Jungebluth, Philipp; Parak, Wolfgang J

    2016-10-15

    The use of nanotechnologies involving nano- and microparticles has increased tremendously in the recent past. There are various beneficial characteristics that make particles attractive for a wide range of technologies. However, colloidal particles on the other hand can potentially be harmful for humans and environment. Today, complete understanding of the interaction of colloidal particles with biological systems still remains a challenge. Indeed, their uptake, effects, and final cell cycle including their life span fate and degradation in biological systems are not fully understood. This is mainly due to the complexity of multiple parameters which need to be taken in consideration to perform the nanosafety research. Therefore, we will provide an overview of the common denominators and ideas to achieve universal metrics to assess their safety. The review discusses aspects including how biological media could change the physicochemical properties of colloids, how colloids are endocytosed by cells, how to distinguish between internalized versus membrane-attached colloids, possible correlation of cellular uptake of colloids with their physicochemical properties, and how the colloidal stability of colloids may vary upon cell internalization. In conclusion three main statements are given. First, in typically exposure scenarios only part of the colloids associated with cells are internalized while a significant part remain outside cells attached to their membrane. For quantitative uptake studies false positive counts in the form of only adherent but not internalized colloids have to be avoided. pH sensitive fluorophores attached to the colloids, which can discriminate between acidic endosomal/lysosomal and neutral extracellular environment around colloids offer a possible solution. Second, the metrics selected for uptake studies is of utmost importance. Counting the internalized colloids by number or by volume may lead to significantly different results. Third, colloids

  1. Versatile Route to Colloidal Stability and Surface Functionalization of Hydrophobic Nanomaterials.

    PubMed

    Culver, Heidi R; Steichen, Stephanie D; Herrera-Alonso, Margarita; Peppas, Nicholas A

    2016-06-01

    We introduce a general method for the stabilization and surface functionalization of hydrophobic nanoparticles using an amphiphilic copolymer, poly(maleic anhydride-alt-1-octadecene)-poly(ethylene glycol) methacrylate (PMAO-PEGMA). Coating nanoparticles with PMAO-PEGMA results in colloidally stable nanoparticles decorated with reactive carboxylic acid and methacrylate functionalities, providing a versatile platform for chemical reactions. The versatility and ease of surface functionalization is demonstrated by varying both the core material and the chemistry used. Specifically, the carboxylic acid functionalities are used to conjugate wheat germ agglutinin to conducting polymer nanoparticles via carbodiimide-mediated coupling, and the methacrylate groups are used to link cysteamine to the surface of poly(ε-caprolactone) nanoparticles via thiol-ene click chemistry and to link temperature-responsive polymer shells to the surface of gold nanoparticles via free radical polymerization. PMID:27203863

  2. EDITORIAL: Colloidal dispersions in external fields Colloidal dispersions in external fields

    NASA Astrophysics Data System (ADS)

    Löwen, Hartmut

    2012-11-01

    Colloidal dispersions have long been proven as pivotal model systems for equilibrium phase transition such as crystallization, melting and liquid-gas phase transition. The last decades have revealed that this is also true for nonequilibrium phenomena. In fact, the fascinating possibility to track the individual trajectories of colloidal particles has greatly advanced our understanding of collective behaviour in classical many-body systems and has helped to reveal the underlying physical principles of glass transition, crystal nucleation, and interfacial dynamics (to name just a few typical nonequilibrium effects). External fields can be used to bring colloids out of equilibrium in a controlled way. Different kinds of external fields can be applied to colloidal dispersions, namely shear flow, electric, magnetic and laser-optical fields, and confinement. Typical research areas can be sketched with the by now traditional complexity diagram (figure 1). The complexity of the colloidal system itself as embodied in statistical degrees of freedom is shown on the x-axis while the complexity of the problem posed, namely bulk, an inhomogeneity in equilibrium, steady state nonequilibrium and full time-dependent nonequilibrium are shown on the y-axis. The different external fields which can be imposed are indicated by the different hatched areas. figure1 Figure 1. Diagram of complexity for colloidal dispersions in external fields: while the x-axis shows the complexity of the system, the y-axis shows the complexity of the problem. Regions which can be accessed by different kinds of external fields are indicated. The arrows indicate recent research directions. Active particles are also indicated with a special complexity of internal degrees of freedom [1]. This collection of papers reflects the scientific programme of the International Conference on Colloidal Dispersions in External Fields III (CODEF III) which took place in Bonn-Bad Godesberg from 20-23 March 2012. This was the

  3. Industrial Chemistry and School Chemistry: Making Chemistry Studies More Relevant

    ERIC Educational Resources Information Center

    Hofstein, Avi; Kesner, Miri

    2006-01-01

    In this paper, we present the development and implementation over the period of more than 15 years of learning materials focusing on industrial chemistry as the main theme. The work was conducted in the Department of Science Teaching at the Weizmann Institute of Science, Israel. The project's general goal was to teach chemistry concepts in the…

  4. Hierarchical microstructures formed by bidisperse colloidal suspensions within colloid-in-liquid crystal gels.

    PubMed

    Diestra-Cruz, Heberth; Bukusoglu, Emre; Abbott, Nicholas L; Acevedo, Aldo

    2015-04-01

    Past studies have reported that colloids of a single size dispersed in the isotropic phase of a mesogenic solvent can form colloid-rich networks (and gels) upon thermal quenching of the system across the isotropic-nematic phase boundary of the mesogens. Herein we report the observation and characterization of complex hierarchical microstructures that form when bidisperse colloidal suspensions of nanoparticles (NPs; iron oxide with diameters of 188 ± 20 nm or poly(methyl methacrylate) with diameters of 150 ± 15 nm) and microparticles (MPs; polystyrene with diameters of 2.77 ± 0.20 μm) are dispersed in the isotropic phase of 4-pentyl-4'-cyanobiphenyl (5CB) and thermally quenched. Specifically, we document microstructuring that results from three sequential phase separation processes that occur at distinct temperatures during stepwise cooling of the ternary mixture from its miscibility region. The first phase transition demixes the system into coexisting MP-rich and NP-rich phases; the second promotes formation of a particle network within the MP-rich phase; and the third, which coincides with the isotropic-to-nematic phase transition of 5CB, produces a second colloidal network within the NP-rich phase. We quantified the dynamics of each demixing process by using optical microscopy and Fourier transform image analysis to establish that the phase transitions occur through (i) surface-directed spinodal decomposition, (ii) spinodal decomposition, and (iii) nucleation and growth, respectively. Significantly, the observed series of phase transitions leads to a hierarchical organization of cellular microstructures not observed in colloid-in-liquid crystal gels formed from monodisperse colloids. The results of this study suggest new routes to the synthesis of colloidal materials with hierarchical microstructures that combine large surface areas and organized porosity with potential applications in catalysis, separations, chemical sensing, or tissue engineering. PMID

  5. Assembling patchy nanorods with spheres: limitations imposed by colloidal interactions.

    PubMed

    Pothorszky, Sz; Zámbó, D; Deák, T; Deák, A

    2016-02-14

    For gold nanorods the intrinsic shape-anisotropy offers the prospect of anisotropic assembly, provided that their region-selective surface modification can be realized. Here we developed nanorods with a patchy surface chemistry, featuring positively charged molecules in the tip region and polymer molecules at the sides by careful control of molecule concentrations during ligand exchange. When these patchy nanorods are assembled with small negatively charged spherical particles, electric double layer interaction can direct the assembly of two nanospheres at the opposite ends of the nanorods. The PEG chains promote the selectivity of the procedure. As the size of the nanospheres increases, they start to shift towards the side of the nanorod due to increased van der Waals interaction. When the relative size of the nanospheres is even larger, only a single nanosphere is assembled, but instead of the tip region, they are attached to the side of the nanorods. The apparent cross-over of the region-selectivity can be interpreted in terms of colloidal interactions, i.e. the second spherical particle is excluded due to nanosphere-nanosphere electric double layer repulsion, while the large vdW attraction results in a side positioning of the single adsorbed spherical particle. The results underline the importance of absolute values of the different interaction strengths and length scales in the programmed assembly of patchy nanoscale building blocks. PMID:26795220

  6. Approaches to separations using silica colloidal membranes

    NASA Astrophysics Data System (ADS)

    Ignacio-de Leon, Patricia Anne Argana

    This thesis describes the synthesis and properties of free-standing nanoporous silica colloidal membranes where the molecular transport is controlled on the basis of size, charge, and chiral selectivity. To achieve this, free-standing membranes were prepared from colloidal solutions of silica nanospheres and the nanopore size and surface functionality were varied. First, Au-coated membranes were prepared and the transport of neutral and charged small molecules through Au-coated silica colloidal membranes modified with poly(methacrylic acid) was studied. Polymer length was controlled by polymerization time to produce pH- and ion-responsive brushes inside the nanopores. By monitoring the flux of a diffusing species, it was demonstrated that the polyelectrolyte brush undergoes swelling and collapse when the pH is increased and decreased, respectively. We also observed an expansion and contraction in the absence and presence of counterions, respectively. We also studied the transport of enantiomers of a chiral dye molecule through silica colloidal membranes with attached chiral moieties. We used small molecules and polymers of amino acid derivatives and chiral calixarenes capable of chiral recognition as a result of stereochemically dependent noncovalent interactions with the diffusing molecule. We found that the selectivity remains approximately the same for membranes modified with small molecules and with polymers. This suggests that enantiopermselectivity depends primarily on the strength of noncovalent interactions rather than the availability of recognition sites. Next, the transport of various generations of dendrimers through silica colloidal membranes was studied in a proof-of-concept experiment to demonstrate the size-selectivity of our materials. Smaller dendrimers were found to diffuse faster and selectivity is improved by using smaller nanopores. Finally, the transport of proteins through silica colloidal membranes was studied as a function of nanopore size

  7. Advanced Colloids Experiment (ACE) Science Overview

    NASA Technical Reports Server (NTRS)

    Meyer, William V.; Sicker, Ronald J.; Chiaramonte, Francis P.; Luna, Unique J.; Chaiken, Paul M.; Hollingsworth, Andrew; Secanna, Stefano; Weitz, David; Lu, Peter; Yodh, Arjun; Yunker, Peter; Lohr, Matthew; Gratale, Matthew; Lynch, Matthew; Kodger, Thomas; Piazza, Roberto; Buzzaccaro, Stefano; Cipelletti, Luca; Schall, Peter; Veen, Sandra; Wegdam, Gerhard; Lee, Chand-Soo; Choi, Chang-Hyung; Paul, Anna-Lisa; Ferl, Robert J.; Cohen, Jacob

    2013-01-01

    The Advanced Colloids Experiment is being conducted on the International Space Station (ISS) using the Light Microscopy Module (LMM) in the Fluids Integrated Rack (FIR). Work to date will be discussed and future plans and opportunities will be highlighted. The LMM is a microscope facility designed to allow scientists to process, manipulate, and characterize colloidal samples in micro-gravity where the absence of gravitational settling and particle jamming enables scientists to study such things as:a.The role that disordered and ordered-packing of spheres play in the phase diagram and equation of state of hard sphere systems,b.crystal nucleation and growth, growth instabilities, and the glass transition, c.gelation and phase separation of colloid polymer mixtures,d.crystallization of colloidal binary alloys,e.competition between crystallization and phase separation,f.effects of anisotropy and specific interactions on packing, aggregation, frustration and crystallization,g.effects of specific reversible and irreversible interactions mediated in the first case by hybridization of complementary DNA strands attached to separate colloidal particles,h.Lock and key interactions between colloids with dimples and spheres which match the size and shape of the dimples,i.finding the phase diagrams of isotropic and interacting particles,j.new techniques for complex self-assembly including scenarios for self-replication, k.critical Casimir forces,l.biology (real and model systems) in microgravity,m.etc. By adding additional microscopy capabilities to the existing LMM, NASA will increase the tools available for scientists that fly experiments on the ISS enabling scientists to observe directly what is happening at the particle level. Presently, theories are needed to bridge the gap between what is being observed (at a macroscopic level when photographing samples) with what is happening at a particle (or microscopic) level. What is happening at a microscopic level will be directly

  8. Quantum confined colloidal nanorod heterostructures for solar-to-fuel conversion.

    PubMed

    Wu, Kaifeng; Lian, Tianquan

    2016-07-11

    Solar energy conversion, particularly solar-driven chemical fuel formation, has been intensely studied in the past decades as a potential approach for renewable energy generation. Efficient solar-to-fuel conversion requires artificial photosynthetic systems with strong light absorption, long-lived charge separation and efficient catalysis. Colloidal quantum confined nanoheterostructures have emerged as promising materials for this application because of the ability to tailor their properties through size, shape and composition. In particular, colloidal one-dimensional (1D) semiconductor nanorods (NRs) offer the opportunity to simultaneously maintain quantum confinement in radial dimensions for tunable light absorptions and bulk like carrier transport in the axial direction for long-distance charge separations. In addition, the versatile chemistry of colloidal NRs enables the formation of semiconductor heterojunctions (such as CdSe/CdS dot-in-rod NRs) to separate photogenerated electron-hole pairs and deposition of metallic domains to accept charges and catalyze redox reactions. In this review, we summarize research progress on colloidal NR heterostructures and their applications for solar energy conversion, emphasizing mechanistic insights into the working principle of these systems gained from spectroscopic studies. Following a brief overview of synthesis of various NRs and heterostructures, we introduce their electronic structures and dynamics of exciton and carrier transport and interfacial transfer. We discuss how these exciton and carrier dynamics are controlled by their structures and provide key mechanistic understanding on their photocatalytic performance, including the photo-reduction of a redox mediator (methyl viologen) and light driven H2 generation. We discuss the solar-driven H2 generation mechanism, key efficiency limiting steps, and potential approaches for rational improvement in semiconductor NR/metal heterostructures (such as Pt tipped Cd

  9. Infrared detection with colloidal quantum dots based on interband and intraband transitions

    NASA Astrophysics Data System (ADS)

    Guyot-Sionnest, Philippe

    2015-03-01

    While much research on colloidal quantum dots is focused on their potential as visible emitter or light harvester, this talk will cover our investigations of the mercury chalcogenide colloidal quantum dots in the thermal mid-infrared ranges of 3-5 microns and 8-12 microns where the atmosphere is transparent. HgTe is a zero-gap semiconductor. As a result, colloidal quantum dots (CQD) of sizes between 10 and 20 nm readily lead to infrared gaps tuning between 3 and 12 microns respectively. It is also very promising that infrared photodetection using dried films of these CQDs has now been demonstrated up to 12 microns. Further improvement through chemistry are likely and will be required to raise the detectivity to the level required to transform thermal infrared detection technology. In contrast to HgTe CQDs which tend to be intrinsic, beta-HgS and HgSe CQDs are naturally n-doped, in the first such instance with CQDs. Furthermore, the doping is modulated by modifying the surface composition, and this effect is attributed to the tuning of the energy level with respect to the environment, via the surface electrostatics. With controlled doping, both HgSe and HgS CQDs have now led to the first operation of mid-infrared CQD photodetector based on the intraband absorption. This is a breakthrough in the field of colloidal quantum dots where interband transitions had been exclusively used for the past 30 years. One challenge with both interband and intraband infrared CQDs will be to reduce the nonradiative recombination, which will improve the detectivity as well as allow to use their infrared luminescence.

  10. [Protoplasm, coagulation and colloids : Forgotten chapter in the research history of anesthesia between Zeitgeist and paradigm].

    PubMed

    Perouansky, M

    2015-05-01

    The historically most important mechanistic theories attributed the fundamental cause of anesthesia to interactions betweeen anesthetics and proteins as early as the 1870s. According to the underlying thought, the resulting changes in the consistency of cellular protoplasm were the cause of the anesthetized state of the whole organism.These protoplasm coagulation theories, as they were collectively referred to, brought the contemporary enthusiasm for protoplasm, the rapid advances in colloid chemistry and the unified theory of narcosis proclamed by Claude Bernard under a unified mechanistic theory that reflected the Zeitgeist of the epoch.This research effort, on the intersection of the developing disciplines of cellular biology and colloid chemistry, lasted for almost a century. It involved scientists of worldwide reputation and resulted in a number of elegant theories. Contrary to widespread opinion, proteins and not lipids were recognized and investigated first as the critical molecular target of anesthetics more than a century prior to their much publicized rediscovery in 1984.The protoplasm coagulation theories of anesthesia were pursued after the First World War across ideological trenches by scientists in Europe, the Soviet Union and the United States. They united research in anesthesia with research of fundamental cell biology.In contrast to the much less fruitful lipid theories, protoplasm coagulation theories are largely forgotten without leaving a trace in contemporary discussions of the history of anesthesia. For many tyears, however, they constituted an essential part of fundamental anesthetic research and must therefore be mentioned in any historical review. PMID:25776209

  11. Colloid Mobilization in Two Atlantic Coastal Plain Aquifers: Field Studies

    NASA Astrophysics Data System (ADS)

    Ryan, Joseph N.; Gschwend, Philip M.

    1990-02-01

    The geochemical mechanisms leading to the mobilization of colloids in groundwater were investigated in the Pine Barrens of New Jersey and in rural central Delaware by sampling pairs of wells screened in oxic and anoxic groundwaters in the same geologic formations. Samples were carefully taken at very low flow rates (˜100 mL min-1) to avoid suspending immobilized particles. The colloidal matter was characterized by light-scattering photometry, scanning electron microscopy, energy-dispersive X ray analysis, microelectrophoresis, and Fe, Al, Si, and organic carbon analyses. The colloids, composed primarily of clays, were observed at high concentrations (up to 60 mg colloids/L) in the anoxic groundwaters, while the oxic groundwaters exhibited ≤1 mg colloids/L. Colloidal organic carbon was present in all groundwaters; but under anoxic conditions, one-third to one-half of the total organic carbon was associated with the inorganic colloids. The field evidence indicates that anoxic conditions cause the mobilization of soil colloids by dissolving the ferric oxyhydroxide coatings cementing the clay particles to the aquifer solids. The depletion of oxidized iron on the surfaces of immobile particles and the addition of organic carbon coatings on the soil particles and colloids apparently stabilizes the colloidal suspension in the anoxic groundwaters.

  12. Colloidal mode of transport in the Potomac River watershed

    SciTech Connect

    Maher, I.L.; Foster, G.D.

    1995-12-31

    Similarly to the particulate phase the colloidal phase may play an important role in the organic contaminant transport downstream the river. The colloidal phase consisting of microparticles and micromolecules which are small enough to be mobile and large enough to attract pollutants can absorb nonpolar organic compounds similarly as do soil and sediment particles. To test the hypothesis three river water samples have been analyzed for PAH content in the dissolved, the colloidal, and the particulate phase. The first sample was collected at the Blue Ridge province of Potomac River watershed, at Point of Rocks, the second one in the Pidmont province, at Riverbend Park, and the third sample at Coastal Plane, at Dyke Marsh (Belle Heven marina). In the laboratory environment each water sample was prefiltered to separate the particulate phase form the dissolved and colloidal phase. One part of the prefiltered water sample was ultrafiltered to separate colloids while the second part of the water was Goulden extracted. The separated colloidal phase was liquid-liquid extracted (LLE) while filters containing the suspended solids were Soxhlet extracted. The extracts of the particulate phase, the colloidal phase, and the dissolved plus colloidal phase were analyzed for selected PAHs via GC/MS. It is planned that concentrations of selected PAHs in three phases will be used for calculations of the partition coefficients, the colloid/dissolved partition coefficient and the particle/dissolved partition coefficient. Both partition coefficients will be compared to define the significance of organic contaminant transport by aquatic colloids.

  13. Methods for colloid transport visualization in pore networks

    NASA Astrophysics Data System (ADS)

    Ochiai, Naoyuki; Kraft, Erika L.; Selker, John S.

    2006-12-01

    Prediction of colloid transport in the subsurface is relevant to researchers in a variety of fields such as contaminant transport, wastewater treatment, and bioremediation. Investigations have traditionally relied on column studies whereby mechanistic inferences must be drawn on the basis of colloid behavior at the outlet. Over the past decade, development of noninvasive visualization techniques based on visible light, magnetic resonance, and X rays have provided insight into a number of colloid transport mechanisms by enabling direct observation of individual colloids at the pore scale and colloid concentrations at longer length scales. As research focus shifts from transport of ideal colloids in ideal media such as glass beads to natural colloids in natural porous media, these noninvasive techniques will become increasingly useful for studying the collection of mechanisms at work in heterogeneous pore systems. It is useful at this juncture to review recent progress in colloid transport visualization as a starting point for further development of visualization tools to support investigation of colloids in natural systems. We briefly discuss characteristics of visualization systems currently used to study colloid transport in porous media and review representative microscale and mesoscale visualization studies conducted over the past decade, with additional attention given to two optical visualization systems being developed by the authors.

  14. Application of ESEM to environmental colloids. [Environmental Scanning Electron Microscopy

    SciTech Connect

    Nuttall, H.E.; Kale, R. . Dept. of Chemical/Nuclear Engineering)

    1993-08-01

    Environmental colloids are toxic or radioactive particles suspended in ground or surface water. These hazardous particles can facilitate and accelerate the transport of toxicants and enhance the threat to humans by exposure to pathogenic substances. The chemical and physical properties of hazardous colloids have not been well characterized nor are there standard colloid remediation technologies to prevent their deleterious effects. Colloid characterization requires measurement of their size distribution, zeta potential, chemical composition, adsorption capacity and morphology. The environmental scanning electron microscope (ESEM) by ElectroScan, Inc., analyzes particle sizes, composition, and morphology. It is also used in this study to identify the attachment of colloids onto packing or rock surfaces in the development of a colloid remediation process. The ESEM has confirmed the composition of groundwater colloids in these studies to be generally the same material as the surrounding rock. The morphology studies have generally shown that colloids are simply small pieces of the rock surface that have exfoliated into the surrounding water. However, in general, the source and chemical composition of groundwater colloids is site dependent. The authors have found that an ESEM works best as a valuable analysis tool within a suite of colloid characterization instruments.

  15. Cotransport of bismerthiazol and montmorillonite colloids in saturated porous media

    NASA Astrophysics Data System (ADS)

    Shen, Chongyang; Wang, Hong; Lazouskaya, Volha; Du, Yichun; Lu, Weilan; Wu, Junxue; Zhang, Hongyan; Huang, Yuanfang

    2015-06-01

    While bismerthiazol [N,N‧-methylene-bis-(2-amino-5-mercapto-1,3,4-thiadiazole)] is one of the most widely used bactericides, the transport of bismerthiazol in subsurface environments is unclear to date. Moreover, natural colloids are ubiquitous in the subsurface environments. The cotransport of bismerthiazol and natural colloids has not been investigated. This study conducted laboratory column experiments to examine the transport of bismerthiazol in saturated sand porous media both in the absence and presence of montmorillonite colloids. Results show that a fraction of bismerthiazol was retained in sand and the retention was higher at pH 7 than at pH 4 and 10. The retention did not change with ionic strength. The retention was attributed to the complex of bismerthiazol with metals/metal oxides on sand surfaces through ligand exchange. The transport of bismerthiazol was enhanced with montmorillonite colloids copresent in the solutions and, concurrently, the transport of montmorillonite colloids was facilitated by the bismerthiazol. The transport of montmorillonite colloids was enhanced likely because the bismerthiazol and the colloids competed for the attachment/adsorption sites on collector surfaces and the presence of bismerthiazol changed the Derjaguin-Landau-Verwey-Overbeek (DLVO) interaction energies between colloids and collectors. The transport of bismerthiazol was inhibited if montmorillonite colloids were pre-deposited in sand because bismerthiazol could adsorb onto the colloid surfaces. The adsorbed bismerthiazol could be co-remobilized with the colloids from primary minima by decreasing ionic strength. Whereas colloid-facilitated transport of pesticides has been emphasized, our study implies that transport of colloids could also be facilitated by the presence of pesticides.

  16. Shape recognition of microbial cells by colloidal cell imprints

    NASA Astrophysics Data System (ADS)

    Borovička, Josef; Stoyanov, Simeon D.; Paunov, Vesselin N.

    2013-08-01

    We have engineered a class of colloids which can recognize the shape and size of targeted microbial cells and selectively bind to their surfaces. These imprinted colloid particles, which we called ``colloid antibodies'', were fabricated by partial fragmentation of silica shells obtained by templating the targeted microbial cells. We successfully demonstrated the shape and size recognition between such colloidal imprints and matching microbial cells. High percentage of binding events of colloidal imprints with the size matching target particles was achieved. We demonstrated selective binding of colloidal imprints to target microbial cells in a binary mixture of cells of different shapes and sizes, which also resulted in high binding selectivity. We explored the role of the electrostatic interactions between the target cells and their colloid imprints by pre-coating both of them with polyelectrolytes. Selective binding occurred predominantly in the case of opposite surface charges of the colloid cell imprint and the targeted cells. The mechanism of the recognition is based on the amplification of the surface adhesion in the case of shape and size match due to the increased contact area between the target cell and the colloidal imprint. We also tested the selective binding for colloid imprints of particles of fixed shape and varying sizes. The concept of cell recognition by colloid imprints could be used for development of colloid antibodies for shape-selective binding of microbes. Such colloid antibodies could be additionally functionalized with surface groups to enhance their binding efficiency to cells of specific shape and deliver a drug payload directly to their surface or allow them to be manipulated using external fields. They could benefit the pharmaceutical industry in developing selective antimicrobial therapies and formulations.

  17. Narrow bandgap colloidal metal chalcogenide quantum dots: synthetic methods, heterostructures, assemblies, electronic and infrared optical properties.

    PubMed

    Kershaw, Stephen V; Susha, Andrei S; Rogach, Andrey L

    2013-04-01

    The chemistry, material processing and fundamental understanding of colloidal semiconductor nanocrystals (quantum dots) are advancing at an astounding rate, bringing the prospects of widespread commercialization of these novel and exciting materials ever closer. Interest in narrow bandgap nanocrystals in particular has intensified in recent years, and the results of research worldwide point to the realistic prospects of applications for these materials in solar cells, infrared optoelectronics (e.g. lasers, optical modulators, photodetectors and photoimaging devices), low cost/large format microelectronics, and in biological imaging and biosensor systems to name only some technologies. Improvements in fundamental understanding and material quality are built on a vast body of experience spread over many different methods of colloidal synthetic growth, each with their own strengths and weaknesses for different materials and sometimes with regard to particular applications. The nanocrystal growth expertise is matched by a rapidly expanding, and highly interdisciplinary, understanding of how best to assemble these materials into films or hybrid composites and thereby into useful devices, and again there are many different strategies that can be adopted. In this review we have attempted to survey and compare the recent work on colloidal synthesis, film and nanocrystal composite material fabrication, concentrating on narrow bandgap chalcogenide materials and some of their topical applications in the solar energy and biological fields. Since these applications are attracting rising interest across a wide range of disciplines, from the biological sciences, device engineering, and materials processing fields as well as the physics and synthetic chemistry communities, we have endeavoured to make the review of these narrow bandgap nanomaterials both comprehensive and accessible to newcomers to the area. PMID:23361653

  18. Colloidal pseudocapacitor: Nanoscale aggregation of Mn colloids from MnCl2 under alkaline condition

    NASA Astrophysics Data System (ADS)

    Chen, Kunfeng; Xue, Dongfeng; Komarneni, Sridhar

    2015-04-01

    Novel colloidal pseudocapacitors are designed using commercially available MnCl2 salts as starting materials and KOH as electrolyte, where the colloids synthesis and subsequently integrating into practical electrode structures occur at the same spatial and temporal scale. Highly electroactive Mn7O13·5H2O colloids are formed in-situ by electric field assisted chemical coprecipitation in KOH solution. The highly efficient Faradaic redox reactions involving Mn3+ ↔ Mn4+ and Mn2+ ↔ Mn3+ are confirmed in electroactive Mn7O13·5H2O pseudocapacitors, which can deliver high specific capacitance of 2518 F/g based on active Mn cations at current density of 5 A/g. The present results show that instead of one-electron Faradaic reaction, Mn cations in our designed system can lead to two-electron Faradaic reactions. The colloidal pseudocapacitor system involving Mn-based colloids is a novel route to engineer electrochemical performances of inorganic pseudocapacitors.

  19. Slab photonic crystals with dimer colloid bases

    SciTech Connect

    Riley, Erin K.; Liddell Watson, Chekesha M.

    2014-06-14

    The photonic band gap properties for centered rectangular monolayers of asymmetric dimers are reported. Colloids in suspension have been organized into the phase under confinement. The theoretical model is inspired by the range of asymmetric dimers synthesized via seeded emulsion polymerization and explores, in particular, the band structures as a function of degree of lobe symmetry and degree of lobe fusion. These parameters are varied incrementally from spheres to lobe-tangent dimers over morphologies yielding physically realizable particles. The work addresses the relative scarcity of theoretical studies on photonic crystal slabs with vertical variation that is consistent with colloidal self-assembly. Odd, even and polarization independent gaps in the guided modes are determined for direct slab structures. A wide range of lobe symmetry and degree of lobe fusion combinations having Brillouin zones with moderate to high isotropy support gaps between odd mode band indices 3-4 and even mode band indices 1-2 and 2-3.

  20. Microscopic dynamics of synchronization in driven colloids

    PubMed Central

    Juniper, Michael P.N.; Straube, Arthur V.; Besseling, Rut; Aarts, Dirk G.A.L.; Dullens, Roel P.A.

    2015-01-01

    Synchronization of coupled oscillators has been scrutinized for over three centuries, from Huygens' pendulum clocks to physiological rhythms. One such synchronization phenomenon, dynamic mode locking, occurs when naturally oscillating processes are driven by an externally imposed modulation. Typically only averaged or integrated properties are accessible, leaving underlying mechanisms unseen. Here, we visualize the microscopic dynamics underlying mode locking in a colloidal model system, by using particle trajectories to produce phase portraits. Furthermore, we use this approach to examine the enhancement of mode locking in a flexible chain of magnetically coupled particles, which we ascribe to breathing modes caused by mode-locked density waves. Finally, we demonstrate that an emergent density wave in a static colloidal chain mode locks as a quasi-particle, with microscopic dynamics analogous to those seen for a single particle. Our results indicate that understanding the intricate link between emergent behaviour and microscopic dynamics is key to controlling synchronization. PMID:25994921

  1. Polymers at interfaces and in colloidal dispersions.

    PubMed

    Fleer, Gerard J

    2010-09-15

    This review is an extended version of the Overbeek lecture 2009, given at the occasion of the 23rd Conference of ECIS (European Colloid and Interface Society) in Antalya, where I received the fifth Overbeek Gold Medal awarded by ECIS. I first summarize the basics of numerical SF-SCF: the Scheutjens-Fleer version of Self-Consistent-Field theory for inhomogeneous systems, including polymer adsorption and depletion. The conformational statistics are taken from the (non-SCF) DiMarzio-Rubin lattice model for homopolymer adsorption, which enumerates the conformational details exactly by a discrete propagator for the endpoint distribution but does not account for polymer-solvent interaction and for the volume-filling constraint. SF-SCF corrects for this by adjusting the field such that it becomes self-consistent. The model can be generalized to more complex systems: polydispersity, brushes, random and block copolymers, polyelectrolytes, branching, surfactants, micelles, membranes, vesicles, wetting, etc. On a mean-field level the results are exact; the disadvantage is that only numerical data are obtained. Extensions to excluded-volume polymers are in progress. Analytical approximations for simple systems are based upon solving the Edwards diffusion equation. This equation is the continuum variant of the lattice propagator, but ignores the finite segment size (analogous to the Poisson-Boltzmann equation without a Stern layer). By using the discrete propagator for segments next to the surface as the boundary condition in the continuum model, the finite segment size can be introduced into the continuum description, like the ion size in the Stern-Poisson-Boltzmann model. In most cases a ground-state approximation is needed to find analytical solutions. In this way realistic analytical approximations for simple cases can be found, including depletion effects that occur in mixtures of colloids plus non-adsorbing polymers. In the final part of this review I discuss a

  2. Glassy Spin Dynamics in Buckled Colloidal Crystal

    NASA Astrophysics Data System (ADS)

    Zhou, Di; Wang, Feng; Han, Yilong

    Geometric frustration arises when lattice structure prevents simultaneous minimization of local interaction energies. It leads to highly degenerate ground states and complex behaviors in frustrated magnetic materials. Here we experimentally studied buckled 1.5-layer colloidal NIPA microgel crystals confined between parallel plates. Spheres buckled up and down are analogous to antiferromagnetic Ising spins. These spins on the distorted triangular lattice exhibit glassy dynamics at low temperatures. In particular, a spin only has 13 nearest-neighbor configurations, which enables to reveal the correlation between structures and dynamical heterogeneity. Soft modes also localize at high-energy regions. Further, we compared the colloidal spin system with kinetic constrained models (KCMs) and observed dynamical facilitation behaviors including excitations lines in space-time. Similar structures and glassy dynamics are also observed in our simulation of Coulomb charges on a triangular lattice. The work was supported by Grant RGC-GRF601613.

  3. Structure and hydrodynamics of colloidal systems

    NASA Astrophysics Data System (ADS)

    Hayter, John B.

    1986-02-01

    Invited paperColloidal phases (for example, micellar solutions, latex suspensions, ferrofluids and microemulsions) provide excellent model systems with which to test structural and hydrodynamic theories of the liquid state. Interparticle potentials may be attractive or repulsive, and the experimentalist is often free to control the strength, range and symmetry of the interactions. Small-angle neutron scattering (SANS) and small-angle neutron spin-echo (SANSE) provide excellent complementary tools for studying the structure and time-dependence of these systems, where correlation lengths typically vary from about one to several tens of nm. Correlation times are usually in the nsec to μsec range, but may be of order minutes in certain systems. This paper will review some of the current theories and their recent experimental tests, using colloidal systems in which the direct interaction potentials may have spherical, dipolar or cylindrical symmetry and the hydrodynamic interactions may be weak or strong.

  4. Structure and hydrodynamics of colloidal systems

    NASA Astrophysics Data System (ADS)

    Hayter, J. B.

    1985-07-01

    Colloidal phases (for example, micellar solutions, latex suspensions, ferrofluids and microemulsions) provide excellent model systems with which to test structural and hydrodynamic theories of the liquid state. Interparticle potentials may be attractive or repulsive, and the experimentalist is often free to control the strength, range and symmetry of the interactions. Small-angle neutron scattering (SANS) and small-angle neutron spin-echo (SANSE) provide excellent complementary tools for studying the structure and time-dependence of these systems, where correlation lengths typically vary from about one to several tens of nm. Correlation times are usually in the nsec to (MU) sec range, but may be of order minutes in certain systems. This paper will review some of the current theories and their recent experimental tests, using colloidal systems in which the direct interaction potentials may have spherical, dipolar or cylindrical symmetry and the hydrodynamic interactions may be weak or strong.

  5. Functionalized patchy particles using colloidal lenses

    NASA Astrophysics Data System (ADS)

    Middleton, Christine

    2014-03-01

    Colloidal assembly had been limited by the isotropic, nonspecific nature of interactions between spherical colloidal particles. By giving particles patches functionalized with single stranded DNA, these interactions can be made both directional and specific. We create patchy particles by adding patches to spherical emulsion droplets using the depletion interaction. First we make polystyrene particles in the shape of contact lenses to be the patches. The lenses are functionalized with single stranded DNA on their convex side. Then we put the lenses on the surface of oil emulsion droplets using the depletion interaction, creating a patch (or multiple patches) on the surface of each emulsion droplet. The emulsion droplets can now interact with each other in a specific, directional way through DNA functionalized patches.

  6. Collective motion in populations of colloidal robots

    NASA Astrophysics Data System (ADS)

    Bartolo, Denis; Bricard, Antoine; Caussin, Jean-Baptiste; Dauchot, Olivier; Desreumaux, Nicolas

    2014-03-01

    Could the behavior of bacteria swarms, fish schools, and bird flocks be understood within a unified framework? Can one ignore the very details of the interaction mechanisms at the individual level to elucidate how strikingly similar collective motion emerges at the group level in this broad range of motile systems? These seemingly provocative questions have triggered significant advance in the physics and the biology, communities over the last decade. In the physics language these systems, made of motile individuals, can all be though as different realizations of ``active matter.'' In this talk, I will show how to gain more insight into this vivid field using self-propelled colloids as a proxy for motile organism. I will show how to motorize colloidal particles capable of sensing the orientation of their neighbors. Then, I will demonstrate that these archetypal populations display spontaneous transitions to swarming motion, and to global directed motion with very few density and orientation fluctuations.

  7. Knot theory realizations in nematic colloids.

    PubMed

    Čopar, Simon; Tkalec, Uroš; Muševič, Igor; Žumer, Slobodan

    2015-02-10

    Nematic braids are reconfigurable knots and links formed by the disclination loops that entangle colloidal particles dispersed in a nematic liquid crystal. We focus on entangled nematic disclinations in thin twisted nematic layers stabilized by 2D arrays of colloidal particles that can be controlled with laser tweezers. We take the experimentally assembled structures and demonstrate the correspondence of the knot invariants, constructed graphs, and surfaces associated with the disclination loop to the physically observable features specific to the geometry at hand. The nematic nature of the medium adds additional topological parameters to the conventional results of knot theory, which couple with the knot topology and introduce order into the phase diagram of possible structures. The crystalline order allows the simplified construction of the Jones polynomial and medial graphs, and the steps in the construction algorithm are mirrored in the physics of liquid crystals. PMID:25624467

  8. Colloidal cholesteric liquid crystal in spherical confinement.

    PubMed

    Li, Yunfeng; Jun-Yan Suen, Jeffrey; Prince, Elisabeth; Larin, Egor M; Klinkova, Anna; Thérien-Aubin, Héloïse; Zhu, Shoujun; Yang, Bai; Helmy, Amr S; Lavrentovich, Oleg D; Kumacheva, Eugenia

    2016-01-01

    The organization of nanoparticles in constrained geometries is an area of fundamental and practical importance. Spherical confinement of nanocolloids leads to new modes of packing, self-assembly, phase separation and relaxation of colloidal liquids; however, it remains an unexplored area of research for colloidal liquid crystals. Here we report the organization of cholesteric liquid crystal formed by nanorods in spherical droplets. For cholesteric suspensions of cellulose nanocrystals, with progressive confinement, we observe phase separation into a micrometer-size isotropic droplet core and a cholesteric shell formed by concentric nanocrystal layers. Further confinement results in a transition to a bipolar planar cholesteric morphology. The distribution of polymer, metal, carbon or metal oxide nanoparticles in the droplets is governed by the nanoparticle size and yields cholesteric droplets exhibiting fluorescence, plasmonic properties and magnetic actuation. This work advances our understanding of how the interplay of order, confinement and topological defects affects the morphology of soft matter. PMID:27561545

  9. The NASA GSFC MEMS Colloidal Thruster

    NASA Technical Reports Server (NTRS)

    Cardiff, Eric H.; Jamieson, Brian G.; Norgaard, Peter C.; Chepko, Ariane B.

    2004-01-01

    A number of upcoming missions require different thrust levels on the same spacecraft. A highly scaleable and efficient propulsion system would allow substantial mass savings. One type of thruster that can throttle from high to low thrust while maintaining a high specific impulse is a Micro-Electro-Mechanical System (MEMS) colloidal thruster. The NASA GSFC MEMS colloidal thruster has solved the problem of electrical breakdown to permit the integration of the electrode on top of the emitter by a novel MEMS fabrication technique. Devices have been successfully fabricated and the insulation properties have been tested to show they can support the required electric field. A computational finite element model was created and used to verify the voltage required to successfully operate the thruster. An experimental setup has been prepared to test the devices with both optical and Time-Of-Flight diagnostics.

  10. Colloidal cholesteric liquid crystal in spherical confinement

    PubMed Central

    Li, Yunfeng; Jun-Yan Suen, Jeffrey; Prince, Elisabeth; Larin, Egor M.; Klinkova, Anna; Thérien-Aubin, Héloïse; Zhu, Shoujun; Yang, Bai; Helmy, Amr S.; Lavrentovich, Oleg D.; Kumacheva, Eugenia

    2016-01-01

    The organization of nanoparticles in constrained geometries is an area of fundamental and practical importance. Spherical confinement of nanocolloids leads to new modes of packing, self-assembly, phase separation and relaxation of colloidal liquids; however, it remains an unexplored area of research for colloidal liquid crystals. Here we report the organization of cholesteric liquid crystal formed by nanorods in spherical droplets. For cholesteric suspensions of cellulose nanocrystals, with progressive confinement, we observe phase separation into a micrometer-size isotropic droplet core and a cholesteric shell formed by concentric nanocrystal layers. Further confinement results in a transition to a bipolar planar cholesteric morphology. The distribution of polymer, metal, carbon or metal oxide nanoparticles in the droplets is governed by the nanoparticle size and yields cholesteric droplets exhibiting fluorescence, plasmonic properties and magnetic actuation. This work advances our understanding of how the interplay of order, confinement and topological defects affects the morphology of soft matter. PMID:27561545

  11. Particles with changeable topology in nematic colloids.

    PubMed

    Ravnik, Miha; Čopar, Simon; Žumer, Slobodan

    2015-09-01

    We show that nematic colloids can serve as a highly variable and controllable platform for studying inclusions with changeable topology and their effects on the surrounding ordering fields. We explore morphing of toroidal and knotted colloidal particles into effective spheres, distinctively changing their Euler characteristic and affecting the surrounding nematic field, including topological defect structures. With toroidal particles, the inner nematic defect eventually transitions from a wide loop to a point defect (a small loop). Trefoil particles become linked with two knotted defect loops, mutually forming a three component link, that upon tightening transform into a two-component particle-defect loop link. For more detailed topological analysis, Pontryagin-Thom surfaces are calculated and visualised, indicating an interesting cascade of defect rewirings caused by the shape morphing of the knotted particles. PMID:26291540

  12. Particles with changeable topology in nematic colloids

    NASA Astrophysics Data System (ADS)

    Ravnik, Miha; Čopar, Simon; Žumer, Slobodan

    2015-09-01

    We show that nematic colloids can serve as a highly variable and controllable platform for studying inclusions with changeable topology and their effects on the surrounding ordering fields. We explore morphing of toroidal and knotted colloidal particles into effective spheres, distinctively changing their Euler characteristic and affecting the surrounding nematic field, including topological defect structures. With toroidal particles, the inner nematic defect eventually transitions from a wide loop to a point defect (a small loop). Trefoil particles become linked with two knotted defect loops, mutually forming a three component link, that upon tightening transform into a two-component particle-defect loop link. For more detailed topological analysis, Pontryagin-Thom surfaces are calculated and visualised, indicating an interesting cascade of defect rewirings caused by the shape morphing of the knotted particles.

  13. Knot theory realizations in nematic colloids

    PubMed Central

    Čopar, Simon; Tkalec, Uroš; Muševič, Igor; Žumer, Slobodan

    2015-01-01

    Nematic braids are reconfigurable knots and links formed by the disclination loops that entangle colloidal particles dispersed in a nematic liquid crystal. We focus on entangled nematic disclinations in thin twisted nematic layers stabilized by 2D arrays of colloidal particles that can be controlled with laser tweezers. We take the experimentally assembled structures and demonstrate the correspondence of the knot invariants, constructed graphs, and surfaces associated with the disclination loop to the physically observable features specific to the geometry at hand. The nematic nature of the medium adds additional topological parameters to the conventional results of knot theory, which couple with the knot topology and introduce order into the phase diagram of possible structures. The crystalline order allows the simplified construction of the Jones polynomial and medial graphs, and the steps in the construction algorithm are mirrored in the physics of liquid crystals. PMID:25624467

  14. Magnetic Colloids By Pulsed Laser Ablation

    NASA Astrophysics Data System (ADS)

    Pandey, B. K.; Singh, M. K.; Agarwal, A.; Gopal, R.

    2011-06-01

    Colloidal magnetic nanoparticles have been successfully synthesized by nano second pules laser ablation of a cobalt slice immersed in liquid (distilled water) medium. The focused output of 1064 nm wavelength of pulsed Nd: YAG laser operating at 40 mJ/pulse is used for ablation. The liquid enviorment allows formation of colloids with nanoparticles in uniform particle diameter. Synchrotron X-ray powder diffraction (XRD) is used for the study of structural property of synthesized nanoparticles. The magnetic properties of cobalt nanoparticles are also investigated. The coercivity of is found to be 73 Oe. The optical properties have been determined by UV-visible absorption spectroscopy and band gap found to be 2.16 and 3.60 eV.

  15. Structure and hydrodynamics of colloidal systems

    SciTech Connect

    Hayter, J.B.

    1985-07-01

    Colloidal phases (for example, micellar solutions, latex suspensions, ferrofluids and microemulsions) provide excellent model systems with which to test structural and hydrodynamic theories of the liquid state. Interparticle potentials may be attractive or repulsive, and the experimentalist is often free to control the strength, range and symmetry of the interactions. Small-angle neutron scattering (SANS) and small-angle neutron spin-echo (SANSE) provide excellent complementary tools for studying the structure and time-dependence of these systems, where correlation lengths typically vary from about one to several tens of nm. Correlation times are usually in the nsec to ..mu..sec range, but may be of order minutes in certain systems. This paper will review some of the current theories and their recent experimental tests, using colloidal systems in which the direct interaction potentials may have spherical, dipolar or cylindrical symmetry and the hydrodynamic interactions may be weak or strong.

  16. Microscopic dynamics of synchronization in driven colloids.

    PubMed

    Juniper, Michael P N; Straube, Arthur V; Besseling, Rut; Aarts, Dirk G A L; Dullens, Roel P A

    2015-01-01

    Synchronization of coupled oscillators has been scrutinized for over three centuries, from Huygens' pendulum clocks to physiological rhythms. One such synchronization phenomenon, dynamic mode locking, occurs when naturally oscillating processes are driven by an externally imposed modulation. Typically only averaged or integrated properties are accessible, leaving underlying mechanisms unseen. Here, we visualize the microscopic dynamics underlying mode locking in a colloidal model system, by using particle trajectories to produce phase portraits. Furthermore, we use this approach to examine the enhancement of mode locking in a flexible chain of magnetically coupled particles, which we ascribe to breathing modes caused by mode-locked density waves. Finally, we demonstrate that an emergent density wave in a static colloidal chain mode locks as a quasi-particle, with microscopic dynamics analogous to those seen for a single particle. Our results indicate that understanding the intricate link between emergent behaviour and microscopic dynamics is key to controlling synchronization. PMID:25994921

  17. Overview of actinide chemistry in the WIPP

    SciTech Connect

    Borkowski, Marian; Lucchini, Jean - Francois; Richmann, Michael K; Reed, Donald T; Khaing, Hnin; Swanson, Juliet

    2009-01-01

    inorganic complexants are expected to be carbonate/bicarbonate and hydroxide. There are also organic complexants in TRU waste with the potential to strongly influence actinide solubility. (3) Intrinsic and pseudo-actinide colloid formation - Many actinide species in their expected oxidation states tend to form colloids or strongly associate with non actinide colloids present (e.g., microbial, humic and organic). In this context, the relative importance of actinides, based on the TRU waste inventory, with respect to the potential release of actinides from the WIPP, is greater for plutonium and americium, and to less extent for uranium and thorium. The most important oxidation states for WIPP-relevant conditions are III and IV. We will present an update of the literature on WIPP-specific data, and a summary of the ongoing research related to actinide chemistry in the WIPP performed by the Los Alamos National Laboratory (LANL) Actinide Chemistry and Repository Science (ACRSP) team located in Carlsbad, NM [Reed 2007, Lucchini 2007, and Reed 2006].

  18. Chemistry Rocks: Redox Chemistry as a Geologic Tool.

    ERIC Educational Resources Information Center

    Burns, Mary Sue

    2001-01-01

    Applies chemistry to earth science, uses rocks in chemistry laboratories, and teaches about transition metal chemistry, oxidation states, and oxidation-reduction reactions from firsthand experiences. (YDS)

  19. Nanoparticle engineering of colloidal suspension behavior

    NASA Astrophysics Data System (ADS)

    Chan, Angel Thanda

    We investigate the effects of highly charged nanoparticles on the phase behavior, structure, and assembly of colloidal microsphere suspensions. Specifically, by selectively tuning the electrostatic interactions between silica microspheres and polystyrene nanoparticles, we study the behavior of four key systems: (i) strongly repulsive, (ii) haloing, (iii) weakly attractive, and (iv) strongly attractive systems. In each system, a combination of nanoparticle adsorption, zeta potential, and confocal microscopy measurements are carried out to systematically study the effects of nanoparticle volume fraction, microsphere/nanoparticle size ratios, and interparticle interactions on their behavior. Our observations indicate that minimal adsorption of highly charged nanoparticles occurs on like-charged and negligibly-charged microspheres, whereas their extent of association increases dramatically with increasing microsphere-nanoparticle attraction. A rich phase behavior emerges in these systems based on whether the nanoparticle species serve as depletants, haloing, or bridging species. The phase transitions in the haloing system occur at constant nanoparticle volume fractions, φnano, over a broad range of microsphere volume fractions, φmicro . By contrast, the observed transitions in the weakly and strongly attractive mixtures occur at a constant number ratio of nanoparticles per microsphere, Nnano/Nmicro. Important structural differences emerge, which can be exploited in the assembly of colloidal gels for direct ink writing and colloidal crystals on epitaxially patterned substrates. Finally, for the first time, we explore nanoparticle haloing as a new route for stabilizing hydrophobic colloidal drugs in aqueous suspensions media for preparation of injectable pharmaceuticals. These microsphere suspensions exhibit improved stability relative to their surfactant-stabilized counterparts after autoclaving, a critical processing step for this target applications. This research

  20. Colloidal Nanocrystals Fluoresced by Surface Coordination Complexes

    PubMed Central

    Wang, Guan; Ji, Jianwei; Zhang, Xinwen; Zhang, Yan; Wang, Qiangbin; You, Xiaozeng; Xu, Xiangxing

    2014-01-01

    Colloidal Nanocrystals (NCs) with fluorescence originating from surface complexes are successfully prepared. The components of these NCs range from insulator, semiconductor to metal, with either pure phase, doped or core/shell structures. The photoluminescence of these NCs can be reversibly tuned across the visible to infrared spectrum, and even allow multi-color emission. A light emitting device is fabricated and a new in vivo cell imaging method is performed to demonstrate the power of this technology for emerging applications. PMID:24970242

  1. Structure and dynamics of biphasic colloidal mixtures.

    PubMed

    Mohraz, Ali; Weeks, Eric R; Lewis, Jennifer A

    2008-06-01

    We investigate the structure and dynamics of biphasic colloidal mixtures composed of coexisting attractive and repulsive microspheres by confocal microscopy. Attractive gels formed in the presence of repulsive microspheres are more spatially homogeneous and, on average, are both more locally tenuous and have fewer large voids than their unary counterparts. The repulsive microspheres within these mixtures display heterogeneous dynamics, with some species exhibiting freely diffusive Brownian motion while others are trapped within the gel network during aggregation. PMID:18643205

  2. DNA- and AC electric field-assisted assembly of two-dimensional colloidal photonic crystals and their controlled defect insertion

    NASA Astrophysics Data System (ADS)

    Kim, Sejong

    Photonic crystals (PC) are structures in which the refractive index is a periodic function in space. The ability of photonic crystals to localize and manipulate electromagnetic waves has attracted considerable attention from the scientific community. The self-assembly of monodisperse micrometer scale colloidal spheres into hexagonal closed-packed colloidal crystals provides a simple, fast, and cheap materials chemistry approach to PCs. Employing DNA supramolecular recognition, 2-dimensional (2D) photonic crystal monolayer was fabricated with monodisperse polystyrene colloidal microspheres. Amine-terminated DNA oligomers were covalently attached onto carboxy-decorated microspheres and enabled their DNA-functionalization while preserving their colloidal stability and organization properties. Following a capillary-force-assisted organization of DNA-decorated microspheres into close-packed 2D opaline arrays, the first monolayer was immobilized by DNA hybridization. Insertion of vacancies at predetermined sites within the lattice of colloidal crystals is a prerequisite in order to realize high-quality, opaline-based photonic devices. The previously obtained DNA-hybridization type binding of 2D-opaline arrays provides a heat-sensitive "adhesive" between substrate and microspheres within a surrounding aqueous medium that enables tuning the hybridization strength of DNA linker as well as a mechanism to facilitate the removal of unbound microspheres. Focusing a laser beam onto a single microsphere of the opaline array induces localized heating that enables the microsphere to detach, leaving behind vacancies. By repeating this process, line vacancies were successfully obtained. The effects of salt concentration, laser power, light-absorbing dyes, DNA length and refractive index mismatch were investigated and found to correlate with heat-induced DNA dehybridization. In addition, AC (alternating current) electrokinetic force was also utilized to obtain assembly of colloidal

  3. Dynamics of Polymers in Colloidal Flows

    NASA Astrophysics Data System (ADS)

    Chen, Hsieh; Alexander-Katz, Alfredo

    2011-03-01

    This research is motivated by recent studies on the von Willebrand factor (vWF), a large multimeric protein that plays an essential role in the initial stages of blood clotting in blood vessels. Recent experiments substantiated the hypothesis that the vWF is activated by shear stress in blood flow that causes its shape to transform from a compact globule to an extended state, and biological function is obtained only in the extended state. Simple simulations (which only consider a single polymer in bulk shear flow) have successfully reproduced the observed dynamics of the vWF. However, a more refined model is still demanding for the better understanding of the behaviors of this biomolecule in the physiological environments. Here we refine the existing model by adding the drifting colloids into the flows to mimic the presence of the blood cells in the bloodstream. Preliminary result shows that colloids greatly influence the dynamics of the polymers. It is observed that the average extensions of polymers along and perpendicular to the shear flow direction are both increased with the presence of the colloids.

  4. Microfluidic Rheology of Soft Colloidal Suspensions

    NASA Astrophysics Data System (ADS)

    Nordstrom, Kerstin; Arratia, Paulo; Verneuil, Emilie; Gollub, Jerry; Durian, Douglas

    2008-11-01

    The rheology of a suspension of soft colloidal particles is investigated using a pressure-driven flow in a deep 25 μm wide microchannel. The system is composed of N-isopropylacrylamide (NIPA), colloidal microgel particles, suspended in aqueous solution. NIPA is temperature-sensitive in that the hydrodynamic radius of a particle decreases as temperature increases [1]. Therefore, colloidal suspensions of different packing fraction can be obtained simply by varying the temperature using a temperature-controlled stage. We determine the velocity profile and the local shear rate of the suspension using particle image velocimetry (PIV). We have developed methods to accurately infer the suspension shear viscosity and shear stress as a function of shear rate. The dynamical range of shear rates probed is approximately 5 orders of magnitude, ranging from 10-3 to 10^2 s-1. Results show that as the packing fraction is increased towards the jamming point, the velocity profiles are markedly non-Newtonian. Further, near the jamming point, the stress versus shear rate curves show yield stress behavior. [1] Alsayed, A.M., Islam, M.F., Zhang, J., Collings, P.J., Yodh, A.J., Science 309, 1207.-1210 (2005)

  5. Synthesis of metal colloids in inverse microemulsions

    NASA Astrophysics Data System (ADS)

    Barnickel, P.; Wokaun, A.

    Colloidal silver and gold particles have been prepared by reduction of aqueous metal salt solutions in inverse microemulsions. The sols are characterized by absorption spectroscopy and electron microscopy. Ultrasound treatment during reduction results in a narrower size distribution of the colloidal particles, as evidenced by a narrower absorption band. Photochemical silver and gold sol formation, without the addition of a reducing agent, has been observed for inverse microemulsions of metal salt solutions in a medium consisting of dodecyl-heptaethyleneglycol-ether and hexane. The particle sizes determined from electron microscopy have been used as input parameters for the simulation of absorption spectra, based on the electromagnetic theory of localized surface plasmon excitation. For the gold sols a quantitative agreement between experimental and simulated spectra is obtained. With the silver colloids, the observed red-shift of the absorption maximum points to the presence of an ionic layer on the surface of the particles. When this layer is included in the theoretical model, good agreement with the experiment is achieved.

  6. Colloidal particle deposition in turbulent flow

    SciTech Connect

    Morton, D.S.

    1994-05-01

    A theoretical analysis is presented which describes the initial deposition of monodispersed spherical colloidal particles from a steady fully developed turbulent flow onto conduit walls. When the net particle-conduit electrical interaction potential is attractive, particle deposition is shown to be often governed by turbulent hydrodynamics. When the net particle-conduit electrical interaction potential possess a repulsive maximum, particle deposition to first order is uniform and depends solely on electrical interaction effects. The developed theoretical model specialized to orifice deposition with the use of Harwell Flow3D turbulence modelling software qualitatively described the deposition of 0.5 {mu}m silica particles onto glass orifices from an aqueous suspension. The effect of the electrical double layer on the rate of colloidal particle deposition in laminar flow has been described by Spielman and Friedlander (1), Dahneke (2), Bowen et al. (3) and Bowen and Epstein (4). This article describes the extension of their work to colloidal particle deposition under steady fully developed turbulent flow conditions. This article also reports the results of orifice particle deposition experiments which were conducted to qualitatively investigate the developed theoretical model.

  7. Dense colloidal fluids form denser amorphous sediments

    PubMed Central

    Liber, Shir R.; Borohovich, Shai; Butenko, Alexander V.; Schofield, Andrew B.; Sloutskin, Eli

    2013-01-01

    We relate, by simple analytical centrifugation experiments, the density of colloidal fluids with the nature of their randomly packed solid sediments. We demonstrate that the most dilute fluids of colloidal hard spheres form loosely packed sediments, where the volume fraction of the particles approaches in frictional systems the random loose packing limit, φRLP = 0.55. The dense fluids of the same spheres form denser sediments, approaching the so-called random close packing limit, φRCP = 0.64. Our experiments, where particle sedimentation in a centrifuge is sufficiently rapid to avoid crystallization, demonstrate that the density of the sediments varies monotonically with the volume fraction of the initial suspension. We reproduce our experimental data by simple computer simulations, where structural reorganizations are prohibited, such that the rate of sedimentation is irrelevant. This suggests that in colloidal systems, where viscous forces dominate, the structure of randomly close-packed and randomly loose-packed sediments is determined by the well-known structure of the initial fluids of simple hard spheres, provided that the crystallization is fully suppressed. PMID:23530198

  8. An evaporation model of colloidal suspension droplets

    NASA Astrophysics Data System (ADS)

    Sartori, Silvana; Li\\ Nán, Amable; Lasheras, Juan C.

    2009-11-01

    Colloidal suspensions of polymers in water or other solvents are widely used in the pharmaceutical industry to coat tablets with different agents. These allow controlling the rate at which the drug is delivered, taste or physical appearance. The coating is performed by simultaneously spraying and drying the tablets with the colloidal suspension at moderately high temperatures. The spreading of the coating on the pills surface depends on the droplet Webber and Reynolds numbers, angle of impact, but more importantly on the rheological properties of the drop. We present a model for the evaporation of a colloidal suspension droplet in a hot air environment with temperatures substantially lower than the boiling temperature of the carrier fluid. As the liquid vaporizes from the surface, a compacting front advances into the droplet faster than the liquid surface regresses, forming a shell of a porous medium where the particles reach their maximum packing density. While the surface regresses, the evaporation rate is determined by both the rate at which heat is transported to the droplet surface and the rate at which liquid vapor is diffused away from it. This regime continues until the compacting front reaches the center of the droplet, at which point the evaporation rate is drastically reduced.

  9. Composition of estuarine colloidal material: organic components

    USGS Publications Warehouse

    Sigleo, A.C.; Hoering, T.C.; Helz, G.R.

    1982-01-01

    Colloidal material in the size range 1.2 nm to 0.4 ??m was isolated by ultrafiltration from Chesapeake Bay and Patuxent River waters (U.S.A.). Temperature controlled, stepwise pyrolysis of the freeze-dried material, followed by gas chromatographic-mass spectrometric analyses of the volatile products indicates that the primary organic components of this polymer are carbohydrates and peptides. The major pyrolysis products at the 450??C step are acetic acid, furaldehydes, furoic acid, furanmethanol, diones and lactones characteristic of carbohydrate thermal decomposition. Pyrroles, pyridines, amides and indole (protein derivatives) become more prevalent and dominate the product yield at the 600??C pyrolysis step. Olefins and saturated hydrocarbons, originating from fatty acids, are present only in minor amounts. These results are consistent with the composition of Chesapeake phytoplankton (approximately 50% protein, 30% carbohydrate, 10% lipid and 10% nucleotides by dry weight). The pyrolysis of a cultured phytoplankton and natural particulate samples produced similar oxygen and nitrogencontaining compounds, although the proportions of some components differ relative to the colloidal fraction. There were no lignin derivatives indicative of terrestrial plant detritus in any of these samples. The data suggest that aquatic microorganisms, rather than terrestrial plants, are the dominant source of colloidal organic material in these river and estuarine surface waters. ?? 1982.

  10. Equilibrium crystal phases of triblock Janus colloids.

    PubMed

    Reinhart, Wesley F; Panagiotopoulos, Athanassios Z

    2016-09-01

    Triblock Janus colloids, which are colloidal spheres decorated with attractive patches at each pole, have recently generated significant interest as potential building blocks for functional materials. Their inherent anisotropy is known to induce self-assembly into open structures at moderate temperatures and pressures, where they are stabilized over close-packed crystals by entropic effects. We present a numerical investigation of the equilibrium phases of triblock Janus particles with many different patch geometries in three dimensions, using Monte Carlo simulations combined with free energy calculations. In all cases, we find that the free energy difference between crystal polymorphs is less than 0.2 kBT per particle. By varying the patch fraction and interaction range, we show that large patches stabilize the formation of structures with four bonds per patch over those with three. This transition occurs abruptly above a patch fraction of 0.30 and has a strong dependence on the interaction range. Furthermore, we find that a short interaction range favors four bonds per patch, with longer range increasingly stabilizing structures with only three bonds per patch. By quantifying the effect of patch geometry on the stability of the equilibrium crystal structures, we provide insights into the fundamental design rules for constructing complex colloidal crystals. PMID:27609002

  11. Nanosized gismondine grown in colloidal precursor solutions.

    PubMed

    Kecht, J; Mihailova, B; Karaghiosoff, K; Mintova, S; Bein, T

    2004-06-22

    A colloidal molecular sieve with GIS-type structure was prepared from aged aluminosilicate precursor solutions containing tetramethylammonium (TMA) hydroxide under hydrothermal treatment at 100 degrees C. The nucleation and the development of the GIS zeolite structure were studied by dynamic light scattering, scanning electron microscopy, X-ray diffraction, Raman and infrared spectroscopies, and liquid-state NMR spectroscopy. It is shown that the aging at room temperature leads to the formation of subcolloidal particles that incorporate TMA cations and form larger aggregates. After an extended heating of 13 days, a complete transformation from amorphous precursor material to crystalline GIS-type colloidal particles is observed. The mean hydrodynamic radius of the crystalline GIS particles is in the range of 30-50 nm. The specific template-framework interactions influence the spectral features of the TMA cations incorporated in the zeolite structure, thus making possible the use of the corresponding Raman spectra and 13C NMR data for the examination of the crystallinity of GIS-type colloidal particles stabilized in water. PMID:15986662

  12. Theory of dynamic arrest in colloidal mixtures

    NASA Astrophysics Data System (ADS)

    Juárez-Maldonado, R.; Medina-Noyola, M.

    2008-05-01

    We present a first-principles theory of dynamic arrest in colloidal mixtures based on the multicomponent self-consistent generalized Langevin equation theory of colloid dynamics [M. A. Chávez-Rojo and M. Medina-Noyola, Phys. Rev. E 72, 031107 (2005); M. A. Chávez-Rojo and M. Medina-Noyola, Phys. Rev. E76, 039902 (2007)]. We illustrate its application with a description of dynamic arrest in two simple model colloidal mixtures: namely, hard-sphere and repulsive Yukawa binary mixtures. Our results include observation of the two patterns of dynamic arrest, one in which both species become simultaneously arrested and the other involving the sequential arrest of the two species. The latter case gives rise to mixed states in which one species is arrested while the other species remains mobile. We also derive the (”bifurcation” or fixed-point”) equations for the nonergodic parameters of the system, which takes the surprisingly simple form of a system of coupled equations for the localization length of the particles of each species. The solution of this system of equations indicates unambiguously which species is arrested (finite localization length) and which species remains ergodic (infinite localization length). As a result, we are able to draw the entire ergodic-nonergodic phase diagram of the binary hard-sphere mixture.

  13. Colloidal particle deposition in turbulent flow

    NASA Astrophysics Data System (ADS)

    Morton, D. S.

    1994-05-01

    A theoretical analysis is presented which describes the initial deposition of monodispersed spherical colloidal particles from a steady fully developed turbulent flow onto conduit walls. When the net particle-conduit electrical interaction potential is attractive, particle deposition is shown to be often governed by turbulent hydrodynamics. When the net particle-conduit electrical interaction potential possess a repulsive maximum, particle deposition to first order is uniform and depends solely on electrical interaction effects. The developed theoretical model specialized to orifice deposition with the use of Harwell Flow 3D turbulence modelling software qualitatively described the deposition of 0.5 (mu)m silica particles onto glass orifices from an aqueous suspension. The effect of the electrical double layer on the rate of colloidal particle deposition in laminar flow has been described by Spielman and Friedlander, Dahneke, Bowen et al. and Bowen and Epstein. This article describes the extension of their work to colloidal particle deposition under steady fully developed turbulent flow conditions. This article also reports the results of orifice particle deposition experiments which were conducted to qualitatively investigate the developed theoretical model.

  14. Remotely Controlled Mixers for Light Microscopy Module (LMM) Colloid Samples

    NASA Technical Reports Server (NTRS)

    Kurk, Michael A. (Andy)

    2015-01-01

    Developed by NASA Glenn Research Center, the LMM aboard the International Space Station (ISS) is enabling multiple biomedical science experiments. Techshot, Inc., has developed a series of colloid specialty cell systems (C-SPECS) for use in the colloid science experiment module on the LMM. These low-volume mixing devices will enable uniform particle density and remotely controlled repetition of LMM colloid experiments. By automating the experiment process, C-SPECS allow colloid samples to be processed more quickly. In addition, C-SPECS will minimize the time the crew will need to spend on colloid experiments as well as eliminate the need for multiple and costly colloid samples, which are expended after a single examination. This high-throughput capability will lead to more efficient and productive use of the LMM. As commercial launch vehicles begin routine visits to the ISS, C-SPECS could become a significant means to process larger quantities of high-value materials for commercial customers.

  15. Design and elaboration of colloidal molecules: an overview.

    PubMed

    Duguet, Etienne; Désert, Anthony; Perro, Adeline; Ravaine, Serge

    2011-02-01

    The concept of colloidal molecules was first evoked by van Blaaderen in 2003 for describing small non-spherical colloids made of the aggregation of a small number of particles. He predicted original properties to the complex assemblies of such colloids, in particular in optics. This critical review deals with the different strategies reported for creating robust clusters of spherical particles which could mimic the space-filling models of simple conventional molecules. These routes concern either the controlled clustering of preformed colloids directed by coalescence, physical routes, chemical routes, or 2-D/3-D geometrical confinement, or strategies starting from a single colloid which is decorated by satellite colloids by taking advantage of controlled phase separation or nucleation and growth phenomena. These routes are compared from the viewpoint of the accessible shapes, their tunability and scalability (146 references). PMID:21212874

  16. Spatially and temporally reconfigurable assembly of colloidal crystals

    NASA Astrophysics Data System (ADS)

    Kim, Youngri; Shah, Aayush A.; Solomon, Michael J.

    2014-04-01

    The self-assembly of colloidal crystals is important to the production of materials with functional optical, mechanical and conductive properties. Yet, self-assembly methods are limited by their slow kinetics and lack of structural control in space and time. Refinements such as templating and directed assembly partially address the problem, albeit by introducing fixed surface features such as templates or electrodes. A template-free method to reconfigure colloidal crystals simultaneously in three-dimensional space and time would better align work in colloidal assembly with materials applications. Here, we report a photo-induced assembly method that yields regions either filled with colloidal crystals or completely devoid of colloids. The origin of the effect is found to be electrophoresis of colloids generated by photochemistry at an indium tin oxide-coated substrate. Simple optical manipulations are applied to reconfigure these assembly and depletion regions. Thus, the method represents a new kind of template-free, reconfigurable three-dimensional photolithography.

  17. A colloidal singularity reveals the crucial role of colloidal stability for nanomaterials in-vitro toxicity testing: nZVI-microalgae colloidal system as a case study.

    PubMed

    Gonzalo, Soledad; Llaneza, Veronica; Pulido-Reyes, Gerardo; Fernández-Piñas, Francisca; Bonzongo, Jean Claude; Leganes, Francisco; Rosal, Roberto; García-Calvo, Eloy; Rodea-Palomares, Ismael

    2014-01-01

    Aggregation raises attention in Nanotoxicology due to its methodological implications. Aggregation is a physical symptom of a more general physicochemical condition of colloidal particles, namely, colloidal stability. Colloidal stability is a global indicator of the tendency of a system to reduce its net surface energy, which may be achieved by homo-aggregation or hetero-aggregation, including location at bio-interfaces. However, the role of colloidal stability as a driver of ENM bioactivity has received little consideration thus far. In the present work, which focuses on the toxicity of nanoscaled Fe° nanoparticles (nZVI) towards a model microalga, we demonstrate that colloidal stability is a fundamental driver of ENM bioactivity, comprehensively accounting for otherwise inexplicable differential biological effects. The present work throws light on basic aspects of Nanotoxicology, and reveals a key factor which may reconcile contradictory results on the influence of aggregation in bioactivity of ENMs. PMID:25340509

  18. A Colloidal Singularity Reveals the Crucial Role of Colloidal Stability for Nanomaterials In-Vitro Toxicity Testing: nZVI-Microalgae Colloidal System as a Case Study

    PubMed Central

    Fernández-Piñas, Francisca; Bonzongo, Jean Claude; Leganes, Francisco; Rosal, Roberto; García-Calvo, Eloy; Rodea-Palomares, Ismael

    2014-01-01

    Aggregation raises attention in Nanotoxicology due to its methodological implications. Aggregation is a physical symptom of a more general physicochemical condition of colloidal particles, namely, colloidal stability. Colloidal stability is a global indicator of the tendency of a system to reduce its net surface energy, which may be achieved by homo-aggregation or hetero-aggregation, including location at bio-interfaces. However, the role of colloidal stability as a driver of ENM bioactivity has received little consideration thus far. In the present work, which focuses on the toxicity of nanoscaled Fe° nanoparticles (nZVI) towards a model microalga, we demonstrate that colloidal stability is a fundamental driver of ENM bioactivity, comprehensively accounting for otherwise inexplicable differential biological effects. The present work throws light on basic aspects of Nanotoxicology, and reveals a key factor which may reconcile contradictory results on the influence of aggregation in bioactivity of ENMs. PMID:25340509

  19. Inorganic Chemistry Solutions to Semiconductor Nanocrystal Problems

    SciTech Connect

    Alvarado, Samuel R.; Guo, Yijun; Ruberu, T. Purnima A.; Tavasoli, Elham; Vela, Javier

    2014-03-15

    The optoelectronic and chemical properties of semiconductor nanocrystals heavily depend on their composition, size, shape and internal structure, surface functionality, etc. Available strategies to alter these properties through traditional colloidal syntheses and ligand exchange methods place a premium on specific reaction conditions and surfactant combinations. In this invited review, we apply a molecular-level understanding of chemical precursor reactivity to reliably control the morphology, composition and intimate architecture (core/shell vs. alloyed) of semiconductor nanocrystals. We also describe our work aimed at achieving highly selective, low-temperature photochemical methods for the synthesis of semiconductor–metal and semiconductor–metal oxide photocatalytic nanocomposites. In addition, we describe our work on surface modification of semiconductor nanocrystal quantum dots using new approaches and methods that bypass ligand exchange, retaining the nanocrystal's native ligands and original optical properties, as well as on spectroscopic methods of characterization useful in determining surface ligand organization and chemistry. Using recent examples from our group and collaborators, we demonstrate how these efforts have lead to faster, wider and more systematic application of semiconductor nanocrystal-based materials to biological imaging and tracking, and to photocatalysis of unconventional substrates. We believe techniques and methods borrowed from inorganic chemistry (including coordination, organometallic and solid state chemistry) have much to offer in reaching a better understanding of the synthesis, functionalization and real-life application of such exciting materials as semiconductor nanocrystals (quantum dots, rods, tetrapods, etc.).

  20. Multiarm Star Polymers as Model Soft Colloids

    NASA Astrophysics Data System (ADS)

    Vlassopoulos, Dimitris

    2010-03-01

    Over the last decade, star polymers emerged as a useful model colloids that interpolate between polymers and hard sphere colloids. Together with microgels, they represent two benchmark soft colloidal systems, their internal structure being the key difference. Indeed, in the case of stars with open structure, the arms can interpenetrate in dense suspensions. The latter feature, that can be probed experimentally, is responsible for a number of interesting structural and dynamic properties of star polymers that set them apart from microgels. In this talk we present the basic properties of star polymers and focus on their extraordinary behavior in the highly concentrated regime, which is typically glassy. Our rheological and scattering experiments demonstrate unique features of the star glasses. Here we discuss two major ones: (i) Aging after pre-shear (the so-called rejuvenation) proceeds via a two-step process, associated with a fast arm engagement and a slow cooperative (cage) rearrangement. Remarkably, at extremely long times a steady state is observed and the terminal time in these systems can be experimentally accessible (and hence tailored at molecular level), as a consequence of the arms fluctuations. (ii) Multiple glassy states can be obtained when mixing stars with polymers or with other stars. Simultaneous theoretical and simulations work suggests that the softness is at the core of this unexpected behavior where depletion gives rise to glass melting and eventually re-entrant glasses are formed. Construction of a state diagram suggests kinetic pathways for tailoring the flow of soft colloids. These examples outline the importance of particle architecture on colloidal properties. Stars are a representative of a large class of hairy particles. The parallel important developments in mode coupling theory and its verses provide much needed predictive tools and rationalization for a number of phenomena such as those discussed here, as well as the complex

  1. Electric field mediated colloidal assembly and control

    NASA Astrophysics Data System (ADS)

    Juarez, Jaime Javier

    2011-12-01

    This dissertation presents video microscopy measurements and computer simulations of colloidal particle interactions in inhomogeneous, high-frequency AC electric fields. The interactions of particles with each other and inhomogeneous electric fields are quantified as a function of concentration, field amplitude, and frequency. Visual state diagrams show that these interactions in concentrated systems produce quasi-two dimensional microstructures including confined hard disk fluids, oriented dipolar chains, and oriented hexagonal close packed crystals. The interaction of a particle interacting with an electric field is directly measured with analyses of a single diffusing colloid within electric fields in the absence of many body effects. Concentrated systems are characterized in terms of density profiles across the electrode gap and angular pair distribution functions. An inverse Monte Carlo analysis extracted the induced dipole-induced dipole interaction from concentrated measurements. A single adjustable parameter consistently modified the induced dipole-field potential and the induced dipole-induced dipole potential to account for modification of the local electric field as the result of the local particle concentration, frequency and configuration. Confocal laser scanning microscopy (CLSM) perform sensitive measurements of internal three dimensional structure of crystals assembled in an interfacial quadrupole electrode device. Radial distributions as functions of elevation are used to characterize the equilibrium structure. A single adjustable parameter modified known potentials to match Monte Carlo simulations with experiment. The local density from experiment and simulation matched the expected density calculated from a balance of osmotic pressure and dielectrophoretic compression. Simulations qualitatively matched experimental observations of microstructure as a function of field amplitude. Programmable assembly for colloidal crystals is implemented in the

  2. Environmental chemistry: Volume A

    SciTech Connect

    Yen, T.F.

    1999-08-01

    This is an extensive introduction to environmental chemistry for engineering and chemical professionals. The contents of Volume A include a brief review of basic chemistry prior to coverage of litho, atmo, hydro, pedo, and biospheres.

  3. Special Report: Brain Chemistry.

    ERIC Educational Resources Information Center

    Krassner, Michael B.

    1983-01-01

    Chemical actions in the brain result in cognitive, emotional, neuroendocrine, neuromuscular, and/or neurocirculatory effects. Developments in understanding brain chemistry are discussed, considering among others, neurotransmitter chemistry, neuropeptides, drugs and the brain, antidepressants, and actions of minor tranquilizers. (JN)

  4. Chemistry for Potters.

    ERIC Educational Resources Information Center

    Denio, Allen A.

    1980-01-01

    Relates pottery making to chemistry by providing chemical information about clay, its origin, composition, properties, and changes that occur during firing; also describes glaze compositions, examples of redox chemistry, salt glazing, crystalline glazes, and problems in toxicity. (CS)

  5. Organometallic Chemistry of Molybdenum.

    ERIC Educational Resources Information Center

    Lucas, C. Robert; Walsh, Kelly A.

    1987-01-01

    Suggests ways to avoid some of the problems students have learning the principles of organometallic chemistry. Provides a description of an experiment used in a third-year college chemistry laboratory on molybdenum. (TW)

  6. Colloidal Particles at Fluid Interfaces and the Interface of Colloidal Fluids

    NASA Astrophysics Data System (ADS)

    McGorty, Ryan

    Holographic microscopy is a unifying theme in the different projects discussed in this thesis. The technique allows one to observe microscopic objects, like colloids and droplets, in a three-dimensional (3D) volume. Unlike scanning 3D optical techniques, holography captures a sample's 3D information in a single image: the hologram. Therefore, one can capture 3D information at video frame rates. The price for such speed is paid in computation time. The 3D information must be extracted from the image by methods such as reconstruction or fitting the hologram to scattering calculations. Using holography, we observe a single colloidal particle approach, penetrate and then slowly equilibrate at an oil--water interface. Because the particle moves along the optical axis (z-axis) and perpendicular to the interface holography is used to determine its position. We are able to locate the particle's z-position to within a few nanometers with a time resolution below a millisecond. We find that the capillary force pulling the particle into the interface is not balanced by a hydrodynamic force. Rather, a larger-than-viscous dissipation associated with the three-phase contact-line slipping over the particle's surface results in equilibration on time scales orders of magnitude longer than the minute time scales over which our setup allows us to examine. A separate project discussed here also examines colloidal particles and fluid-fluid interfaces. But the fluids involved are composed of colloids. With a colloid and polymer water-based mixture we study the phase separation of the colloid-rich (or liquid) and colloid-poor (or gas) region. In comparison to the oil--water interface in the previously mentioned project, the interface between the colloidal liquid and gas phases has a surface tension nearly six orders of magnitude smaller. So interfacial fluctuations are observable under microscopy. We also use holographic microscopy to study this system but not to track particles with

  7. Internal Dynamics of Equilibrium Colloidal Clusters

    NASA Astrophysics Data System (ADS)

    Perry, Rebecca Wood

    Colloidal clusters, aggregates of a few micrometer-sized spherical particles, are a model experimental system for understanding the physics of self-assembly and processes such as nucleation. Colloidal clusters are well suited for studies on these topics because they are the simplest colloidal system with internal degrees of freedom. Clusters made from particles that weakly attract one another continually rearrange between different structures. By characterizing these internal dynamics and the structures connected by the rearrangement pathways, we seek to understand the statistical physics underlying self-assembly and equilibration. In this thesis, we examine the rearrangement dynamics of colloidal clusters and analyze the equilibrium distributions of ground and excited states. We prepare clusters of up to ten microspheres bound by short-range depletion interactions that are tuned to allow equilibration between multiple isostatic arrangements. To study these clusters, we use bright-field and digital holographic microscopy paired with computational post-processing to amass ensemble-averaged and time-averaged probabilities. We study both two-dimensional (2D) and three-dimensional (3D) clusters composed of either one or two species of particles. To learn about geometrical nucleation barriers, we track rearrangements of particles within freely rotating and translating 3D clusters. We show that rearrangements occur on a timescale of seconds, consistent with diffusion-dominated internal dynamics. To better understand excited states and transition pathways, we track hundreds of rearrangements between degenerate ground states in 2D clusters. We show that the rearrangement rates can be understood using a model with two parameters, which account for the diffusion coefficient along the excited-state rearrangement pathways and the interaction potential. To explore new methods to control self-assembly, we analyze clusters of two species with different masses and different

  8. Oppositely charged colloids out of equilibrium

    NASA Astrophysics Data System (ADS)

    Vissers, T.

    2010-11-01

    Colloids are particles with a size in the range of a few nanometers up to several micrometers. Similar to atomic and molecular systems, they can form gases, liquids, solids, gels and glasses. Colloids can be used as model systems because, unlike molecules, they are sufficiently large to be studied directly with light microscopy and move sufficiently slow to study their dynamics. In this thesis, we study binary systems of polymethylmethacrylate (PMMA) colloidal particles suspended in low-polar solvent mixtures. Since the ions can still partially dissociate, a surface charge builds up which causes electrostatic interactions between the colloids. By carefully tuning the conditions inside the suspension, we make two kinds of particles oppositely charged. To study our samples, we use Confocal Laser Scanning Microscopy (CLSM). The positively and negatively charged particles can be distinguished by a different fluorescent dye. Colloids constantly experience a random motion resulting from random kicks of surrounding solvent molecules. When the attractions between the oppositely charged particles are weak, the particles can attach and detach many times and explore a lot of possible configurations and the system can reach thermodynamic equilibrium. For example, colloidal ‘ionic’ crystals consisting of thousands to millions of particles can form under the right conditions. When the attractions are strong, the system can become kinetically trapped inside a gel-like state. We observe that when the interactions change again, crystals can even emerge again from this gel-like phase. By using local order parameters, we quantitatively study the crystallization of colloidal particles and identify growth defects inside the crystals. We also study the effect of gravity on the growth of ionic crystals by using a rotating stage. We find that sedimentation can completely inhibit crystal growth and plays an important role in crystallization from the gel-like state. The surface

  9. Synthesis and self-assembly of Janus and patchy colloidal particles

    NASA Astrophysics Data System (ADS)

    Jiang, Shan

    Colloidal particles are considered classically as spherical particles with homogeneous surface chemistry. When this is so, the interactions between particles are isotropic and governed only by their separations. One can take advantage of this to simulate atoms, visualizing them one-by-one in a microscope, albeit at a larger length scale and longer time scale than for true atoms. However if the particles are not homogeneous, but Janus or patchy instead, with different surface chemistry on different hemispheres or otherwise different surface sites that are addressably controlled, the interactions between these particles depend not only on their separation, but also on their orientation. Research on Janus and patchy colloidal particles has opened a new chapter in the colloid research field, allowing us to mimic the behavior of these colloidal analogues of molecules, and in this way to ask new and exciting questions of condensed matter physics. In this dissertation, I investigated the synthesis and self-assembly of Janus and patchy colloidal particles with emphasis on Janus amphiphilic particles, which are the colloidal counterpart of surfactant molecules. Improving the scale-up capability, and also the capacity to control the geometry of Janus particles, I developed a simple and versatile method to synthesize Janus particles using an approach based on Pickering emulsions with particles adsorbed at the liquid-liquid interface. I showed that this method can be scaled up to synthesize Janus particles in large quantity. Also, the Janus balance can be predictably controlled by adding surfactant molecules during emulsification. In addition, going beyond the Janus geometry, I developed another synthetic method to fabricate trivalent patchy colloidal particles using micro-contact printing. With these synthetic methods in hand, I explored the self-assembly of Janus amphiphilic particles in aqueous solutions, while controlling systematically the salt concentration, the particle

  10. Study of the stability coated and uncoated nanosilver colloid

    NASA Astrophysics Data System (ADS)

    Harsojo, Respitaningrum, Afrianto, Toto; Sosiati, Harini

    2013-09-01

    The stability of nanosilver colloids made using electrochemical process and chemical process were investigated. In the process using a DC generator cell, two silver electrodes under a DC voltage were used to generate the colloid. In the chemical process the colloid was made using the dilution of AgNO3 in deionized water with the addition of sodium citrate. To increase the stability to this colloid was added polyvinyl alcohol. The stability In those three colloids were investigated using UV-Vis spectrometer. The size of the nano Ag was measured using transmission electron microscope (TEM). The study reveals that within period of two weeks the trend toward a stable colloid is shown by colloid using DC generator. The addition of PVA may stabilize the unstable colloid made using the chemichal process and reduce the size particle to significantly smaller particle compared to the one made using DC generator cell. The condition of obtaining the stable nano colloid silver with smaller particle size was discussed.

  11. Colloid mobilization by fluid displacement fronts in channels.

    PubMed

    Lazouskaya, Volha; Wang, Lian-Ping; Or, Dani; Wang, Gang; Caplan, Jeffrey L; Jin, Yan

    2013-09-15

    Understanding colloid mobilization during transient flow in soil is important for addressing colloid and contaminant transport issues. While theoretical descriptions of colloid detachment exist for saturated systems, corresponding mechanisms of colloid mobilization during drainage and imbibition have not been considered in detail. In this work, theoretical force and torque analyses were performed to examine the interactive effects of adhesion, drag, friction, and surface tension forces on colloid mobilization and to outline conditions corresponding to the mobilization mechanisms such as lifting, sliding, and rolling. Colloid and substrate contact angles were used as variables to determine theoretical criteria for colloid mobilization mechanisms during drainage and imbibition. Experimental mobilization of hydrophilic and hydrophobic microspheres with drainage and imbibition fronts was investigated in hydrophilic and hydrophobic channels using a confocal microscope. Colloid mobilization differed between drainage and imbibition due to different dynamic contact angles and interfacial geometries on the contact line. Experimental results did not fully follow the theoretical criteria in all cases, which was explained with additional factors not included in the theory such as presence of aggregates and trailing films. Theoretical force and torque analyses resulted in similar mobilization predictions and suggested that all mobilization mechanisms contributed to the observed colloid mobilization. PMID:23800372

  12. Statics and dynamics of colloidal particles on optical tray arrays

    SciTech Connect

    Reichardt, Charles; Reichhardt, Cynthia J

    2009-01-01

    We examine the statics and dynamics of charged colloids interacting with periodic optical trap arrays. In particular we study the regime where more than one colloid is confined in each trap, creating effective dimer, trimer, and higher order states called colloidal molecular crystals. The n-mer states have all effective orientational degree of freedom which can be controlled with an external driving field. In general, the external field causes a polarization effect where the orientation of the n-mers aligns with the external field, similar to liquid crystal systems. Additionally, under a rotating external drive the n-mers can rotate with the drive. In some cases a series of structural transitions in the colloidal crystal states occur in the rotating field due to a competition between the ordering of the colloidal molecular crystals and the polarization effect which orients the n-mers in the direction of the drive. We also show that for some parameters, the n-mers continuously rotate with the drive without witching, that depinning transitions can occur where the colloids jump from well to well, and that there are a number of distinct dynamical transitions between the phases. Finally, we illustrate colloidal orderings at fillings of more than four colloids per trap, indicating that it is possible to create higher order colloidal crystal cluster phases.

  13. Sodium meta-autunite colloids: Synthesis, characterization,stability

    SciTech Connect

    zzuoping@lbl.gov

    2004-04-10

    Waste forms of U such as those in the United States Department of Energy's Hanford Site often contain high concentrations of Na and P. Low solubility sodium uranyl phosphates such as sodium meta-autunite have the potential to form mobile colloids that can facilitate transport of this radionuclide. In order to understand the geochemical behavior of uranyl phosphate colloids, we synthesized sodiummeta-autunite colloids, and characterized their morphology, chemical composition, structure, dehydration, and surface charge. The stability of these synthetic plate-shaped colloids was tested with respect to time and pH. The highest aggregation rate was observed at pH 3, and the rate decreases as pH increases, indicating that higher stability of colloid dispersion under neutral and alkaline pH conditions. The synthetic colloids are all negatively charged and no isoelectric points were found over a pH range of 3 to 9. The zeta-potentials of the colloids in the phosphate solution show a strong pH-dependence in the more acidic range over time, but are relatively constant in the neutral and alkaline pH range. The geochemical behavior of the synthetic colloids can be interpreted using DLVO theory. The results suggest that formation of mobile sodium meta-autunite colloids can enhance the transport of U in some contaminated sediments.

  14. Tuning Colloid-Interface Interactions by Salt Partitioning.

    PubMed

    Everts, J C; Samin, S; van Roij, R

    2016-08-26

    We show that the interaction of an oil-dispersed colloidal particle with an oil-water interface is highly tunable from attractive to repulsive, either by varying the sign of the colloidal charge via charge regulation or by varying the difference in hydrophilicity between the dissolved cations and anions. In addition, we investigate the yet unexplored interplay between the self-regulated colloidal surface charge distribution with the planar double layer across the oil-water interface and the spherical one around the colloid. Our findings explain recent experiments and have direct relevance for tunable Pickering emulsions. PMID:27610887

  15. Analysis of colloidal phases in urban stormwater runoff

    SciTech Connect

    Grout, H.; Wiesner, M.R.; Bottero, J.Y.

    1999-03-15

    The composition and morphology of colloidal materials entering an urban waterway (Brays Bayou, Houston, USA) during a storm event was investigated. Analyses of organic carbon, Si, Al, Fe, Cr, Cu, Mn, Zn, Ca, Mg, and Ba were performed on the fraction of materials passing through a 0.45 {micro}m filter. This fraction, traditionally defined as dissolved, was further fractionated by ultracentrifugation into colloidal and dissolved fractions. Colloids, operationally defined by this procedure, accounted for 17% of the carbon, 32% of the silica, 79% of the Al, 85% of the Fe, 52% of the Cr, 43% of the Mn, and 29% of the Zn present in filtrates when averaged over the storm event. However, the composition of colloidal material was observed to change over time. For example, colloids were predominantly composed of silica during periods of dry weather flow and at the maximum of the stormwater flow, while carbon dominated the colloidal fraction at the beginning and declining stages of the storm event. These changes in colloidal composition were accompanied by changes in colloidal morphologies, varying from organic aggregates to diffuse gel-like structures rich in Si, Al, and Fe. The colloidal phase largely determined the variability of elements in the 0.45 {micro}m filtrate.

  16. Zero-valent iron colloid emplacement in sand columns

    SciTech Connect

    Cantrell, K.J.; Kaplan, D.I.

    1997-05-01

    Application of chemically reactive barriers to mitigate contaminant migration is an active area of research and development. Studies were conducted to evaluate a novel approach of emplacing chemically reactive barriers composed of zero-valent iron (Fe{sup 0}) by injecting suspensions of colloidal-size Fe{sup 0} particles into porous media. The specific objective of this study was to evaluate the effect of influent colloid concentration, rate, and volume of colloidal suspensions on Fe{sup 0} colloid emplacement in sand columns. Relatively even distributions of Fe{sup 0} throughout a sand column were obtained at low influent colloid concentrations and high injection rates. As the concentration of influent suspensions was increased, a point was reached beyond which a significant increase in the filtration of Fe{sup 0} particles near the front of the column was observed. This point was also found to occur at lower influent colloid concentrations as the injection rate was decreased, i.e., there was an interactive effect of influent colloid concentration and injection rate on the extent of filtration that occurred near the front of the column. As the volume of the colloidal suspension injected into the column was increased, the distribution of Fe{sup 0} colloids within the column became increasingly even.

  17. Three-dimensional colloidal crystals in liquid crystalline blue phases

    PubMed Central

    Ravnik, Miha; Alexander, Gareth P.; Yeomans, Julia M.; Žumer, Slobodan

    2011-01-01

    Applications for photonic crystals and metamaterials put stringent requirements on the characteristics of advanced optical materials, demanding tunability, high Q factors, applicability in visible range, and large-scale self-assembly. Exploiting the interplay between structural and optical properties, colloidal lattices embedded in liquid crystals (LCs) are promising candidates for such materials. Recently, stable two-dimensional colloidal configurations were demonstrated in nematic LCs. However, the question as to whether stable 3D colloidal structures can exist in an LC had remained unanswered. We show, by means of computer modeling, that colloidal particles can self-assemble into stable, 3D, periodic structures in blue phase LCs. The assembly is based on blue phases providing a 3D template of trapping sites for colloidal particles. The particle configuration is determined by the orientational order of the LC molecules: Specifically, face-centered cubic colloidal crystals form in type-I blue phases, whereas body-centered crystals form in type-II blue phases. For typical particle diameters (approximately 100 nm) the effective binding energy can reach up to a few 100 kBT, implying robustness against mechanical stress and temperature fluctuations. Moreover, the colloidal particles substantially increase the thermal stability range of the blue phases, for a factor of two and more. The LC-supported colloidal structure is one or two orders of magnitude stronger bound than, e.g., water-based colloidal crystals. PMID:21368186

  18. Electrochromism with colloidal WO3 and IrO2

    NASA Astrophysics Data System (ADS)

    Michalak, Franck; Rault, L.; Aldebert, Pierre

    1992-11-01

    Colloidal particles of WO3 and IrO2 are synthesized and dispersed within a gelatinous perfluorinated ionomer matrix. Experimental procedures are established in order to obtain percolation between the electrochromic particles. Colloidal particle sizes are measured by quasi elastic light scattering. Electrochemical properties of the mixed colloid electrodes are determined by cyclic voltammetry and impedance spectroscopy. Preliminary optical tests are performed in order to measure transmission and contrast of electrochromic half cells with a mixed colloid electrode, and also a sputtered oxide electrode.

  19. Infrared colloidal lead chalcogenide nanocrystals: synthesis, properties, and photovoltaic applications.

    PubMed

    Fu, Huiying; Tsang, Sai-Wing

    2012-04-01

    Simple solution phase, catalyst-free synthetic approaches that offer monodispersed, well passivated, and non-aggregated colloidal semiconductor nanocrystals have presented many research opportunities not only for fundamental science but also for technological applications. The ability to tune the electrical and optical properties of semiconductor nanocrystals by manipulating the size and shape of the crystals during the colloidal synthesis provides potential benefits to a variety of applications including photovoltaic devices, light-emitting diodes, field effect transistors, biological imaging/labeling, and more. Recent advances in the synthesis and characterization of colloidal lead chalcogenide nanocrystals and the achievements in colloidal PbS or PbSe nanocrystals solar cells have demonstrated the promising application of infrared-emitting colloidal lead chalcogenide nanocrystals in photovoltaic devices. Here, we review recent progress in the synthesis and optical properties of colloidal lead chalcogenide nanocrystals. We focus in particular upon the size- and shape-controlled synthesis of PbS, PbSe, and PbTe nanocrystals by using different precursors and various stabilizing surfactants for the growth of the colloidal nanocrystals. We also summarize recent advancements in the field of colloidal nanocrystals solar cells based on colloidal PbS and PbSe nanocrystals. PMID:22382898

  20. Colloid formation and laser-induced bleaching in fluorite

    SciTech Connect

    LeBret, Joel B.; Cramer, Loren P.; Norton, M. Grant; Dickinson, J. T.

    2004-11-08

    Colloid formation and subsequent laser-induced bleaching in fluorite has been studied by transmission electron microscopy and electron diffraction. At high incident electron-beam (e-beam) energies, Ca colloids with diameter {approx}10 nm form a simple cubic superlattice with lattice parameter a{approx}18 nm. The colloids themselves are topotactic with the fluorite matrix forming low-energy interfaces close to a {sigma}=21 special grain boundary in cubic materials. Laser irradiation using {lambda}=532 nm has been shown to effectively bleach the e-beam-irradiated samples returning the fluorite to its monocrystalline state. The bleached samples appear more resistant to further colloid formation.

  1. Fabrication and characterization of colloidal crystal thin films

    NASA Astrophysics Data System (ADS)

    Rodríguez, I.; Ramiro-Manzano, F.; Meseguer, F.; Bonet, E.

    2011-03-01

    We present a laboratory experiment that allows undergraduate or graduate students to get introduced to colloidal crystal research concepts in an interesting way. Moreover, such experiments and studies can also be useful in the field of crystallography or solid-state physics. The work concerns the growth of colloidal crystal thin films obtained from the crystallization of a latex colloidal solution in a wedge cell. Depending on the thickness of the sample, microcrystals with different structures and orientation are obtained. Colloidal arrangements are studied by scanning electronic microscopy images of the top and edge views of several areas of the crystals.

  2. Switching light with light - advanced functional colloidal monolayers

    NASA Astrophysics Data System (ADS)

    Bley, K.; Sinatra, N.; Vogel, N.; Landfester, K.; Weiss, C. K.

    2013-12-01

    Colloidal monolayers comprising of highly ordered two dimensional crystals are of high interest to generate surface patterns for a variety of different applications. Mostly, unfunctionalized polymer or silica colloids are assembled into monolayers. However, the incorporation of functional molecules into such colloids offers a convenient possibility of implementing additional properties to the two-dimensional crystal. Here, we present the formation of novel functional colloidal monolayers with photoswitchable fluorescence. The miniemulsion polymerization technique was used to incorporate an appropriate dye system of a perylene-based fluorophore and a bis-arylethene as a photochrome in polymeric colloids in defined ratios. Upon irradiation with UV or visible light the photochrome reversibly isomerizes from the ring-closed form, which is able to absorb light of the emission wavelength of the fluorescent dye and the ring-open form, which is not. The fluorescence emission of the dye can thus be reversibly switched on and off with light even when embedded in colloids. The colloids were self-assembled at the air-water interface to produce hexagonally ordered functional monolayers and more complex binary crystals. We investigate in detail the influence of the polymeric matrix on the switching properties of the fluorophore/photochrome system and find that the rate constants for the photoswitching, which all lie in the same range, are less influenced by the polymeric environment than expected. We demonstrate the reversible switching of the fluorescence emission in self-assembled colloidal monolayers. The arrangement of broadly distributed functional colloids into ordered monolayers with high addressability was obtained by the formation of binary colloidal monolayers.Colloidal monolayers comprising of highly ordered two dimensional crystals are of high interest to generate surface patterns for a variety of different applications. Mostly, unfunctionalized polymer or silica

  3. Characterization of colloidal silica and its adsorption phenomenon with silicon-base surfactants with relation to film strength

    SciTech Connect

    Fariza, H.; Huang, D.

    1996-10-01

    Colloidal silica has been used for film formation in many industrial applications. The film strength depends on the siloxane bond formation, which is modulated by the surfactants present in the system. The adsorption of surfactants on surface of silica dispersed in aqueous systems affects its surface properties - well as physical and chemical reactions. Colloidal silica, having surface silanol groups can interact with the hydrophilic end of surfactant molecules through H-bonding. A commonly used surfactant, a polyalkylene oxide-modified polydimethylsiloxane, affects the reactions of silica under various conditions. A systematic study of silica and its chemistry in presence of the surfactant show that the surface properties of silica particles influence hydrogen bonding of silanols and adsorption of the surfactant. The level of surfactant adsorption on silica modifies the film strength by changing the extent of siloxane bond formed between two silicon atoms.

  4. Chemistry and Art.

    ERIC Educational Resources Information Center

    Berry, Martyn

    1999-01-01

    Describes a Chemistry and Art project developed for secondary students and teachers sponsored by the National Gallery and The Royal Society of Chemistry in the United Kingdom. Discusses aspects of the techniques used in creating five paintings as well as the chemistry involved in their making, deterioration, conservation, and restoration.…

  5. Teaching School Chemistry.

    ERIC Educational Resources Information Center

    Waddington, D. J., Ed.

    This eight-chapter book is intended for use by chemistry teachers, curriculum developers, teacher educators, and other key personnel working in the field of chemical education. The chapters are: (1) "The Changing Face of Chemistry" (J. A. Campbell); (2) "Curriculum Innovation in School Chemistry" (R. B. Ingel and A. M. Ranaweera); (3) "Some…

  6. Green Chemistry and Education.

    ERIC Educational Resources Information Center

    Hjeresen, Dennis L.; Schutt, David L.; Boese, Janet M.

    2000-01-01

    Many students today are profoundly interested in the sustainability of their world. Introduces Green Chemistry and its principles with teaching materials. Green Chemistry is the use of chemistry for pollution prevention and the design of chemical products and processes that are environmentally benign. (ASK)

  7. Environmental Chemistry Activities.

    ERIC Educational Resources Information Center

    Jackland, Thomas; And Others

    The authors of this curriculum supplement believe in a laboratory approach to chemistry and express the feeling that environmental chemistry provides the students an opportunity to apply theoretical chemistry to important practical problems. There are eighteen activities presented, each accompanied with behavioral objectives, one or more suggested…

  8. Chemistry on Stamps.

    ERIC Educational Resources Information Center

    Schreck, James O.

    1986-01-01

    Suggests how postage stamps can be incorporated into chemistry teaching. Categories considered include emergence of chemistry as a science, metric system, atoms (and molecules and ions), stoichiometry, energy relationships in chemical systems, chemical bonding, nuclear chemistry, biochemistry, geochemistry, matter (gases, liquids, and solids),…

  9. Chemistry as General Education

    ERIC Educational Resources Information Center

    Tro, Nivaldo J.

    2004-01-01

    The efficacy of different science and chemistry courses for science-major and non-major students, and the question of chemistry's contribution to general education are evaluated. Chemistry and science curriculum are too profession- and consumer-oriented, and to overcome this problem, it is advised that all disciplines must incorporate the major…

  10. History of Chemistry.

    ERIC Educational Resources Information Center

    Servos, John W.

    1985-01-01

    Discusses the development of chemistry in the United States by considering: (1) chemistry as an evolving body of ideas/techniques, and as a set of conceptual resources affecting and affected by the development of other sciences; and (2) chemistry related to the history of American social and economic institutions and practices. (JN)

  11. Wavefunction engineering: From quantum wells to near-infrared type-II colloidal quantum dots synthesized by layer-by-layer colloidal epitaxy.

    PubMed

    Li, J Jack; Tsay, James M; Michalet, Xavier; Weiss, Shimon

    2005-11-15

    We review the concept and the evolution of bandgap and wavefunction engineering, the seminal contributions of Dr. Chemla to the understanding of the rich phenomena displayed in epitaxially grown quantum confined systems, and demonstrate the application of these concepts to the colloidal synthesis of high quality type-II CdTe/CdSe quantum dots using successive ion layer adsorption and reaction chemistry. Transmission electron microscopy reveals that CdTe/CdSe can be synthesized layer by layer, yielding particles of narrow size distribution. Photoluminescence emission and excitation spectra reveal discrete type-II transitions, which correspond to energy lower than the type-I bandgap. The increase in the spatial separation between photoexcited electrons and holes as a function of successive addition of CdSe monolayers was monitored by photoluminescence lifetime measurements. Systematic increase in lifetimes demonstrates the high level of wavefunction engineering and control in these systems. PMID:22865949

  12. School Chemistry vs. Chemistry in Research: An Exploratory Experiment.

    ERIC Educational Resources Information Center

    Habraken, Clarisse L.; Buijs, Wim; Borkent, Hens; Ligeon, Willy; Wender, Harry; Meijer, Marijn

    2001-01-01

    Reports on a study exploring why students are not studying chemistry. Three groups of graduating high school students and their chemistry teachers stayed at a research institute working on molecular modeling and wrote essays on school chemistry versus chemistry in research. Concludes that school chemistry does not convey today's chemistry in…

  13. Switching light with light - advanced functional colloidal monolayers

    NASA Astrophysics Data System (ADS)

    Bley, K.; Sinatra, N.; Vogel, N.; Landfester, K.; Weiss, C. K.

    2013-12-01

    Colloidal monolayers comprising of highly ordered two dimensional crystals are of high interest to generate surface patterns for a variety of different applications. Mostly, unfunctionalized polymer or silica colloids are assembled into monolayers. However, the incorporation of functional molecules into such colloids offers a convenient possibility of implementing additional properties to the two-dimensional crystal. Here, we present the formation of novel functional colloidal monolayers with photoswitchable fluorescence. The miniemulsion polymerization technique was used to incorporate an appropriate dye system of a perylene-based fluorophore and a bis-arylethene as a photochrome in polymeric colloids in defined ratios. Upon irradiation with UV or visible light the photochrome reversibly isomerizes from the ring-closed form, which is able to absorb light of the emission wavelength of the fluorescent dye and the ring-open form, which is not. The fluorescence emission of the dye can thus be reversibly switched on and off with light even when embedded in colloids. The colloids were self-assembled at the air-water interface to produce hexagonally ordered functional monolayers and more complex binary crystals. We investigate in detail the influence of the polymeric matrix on the switching properties of the fluorophore/photochrome system and find that the rate constants for the photoswitching, which all lie in the same range, are less influenced by the polymeric environment than expected. We demonstrate the reversible switching of the fluorescence emission in self-assembled colloidal monolayers. The arrangement of broadly distributed functional colloids into ordered monolayers with high addressability was obtained by the formation of binary colloidal monolayers.Colloidal monolayers comprising of highly ordered two dimensional crystals are of high interest to generate surface patterns for a variety of different applications. Mostly, unfunctionalized polymer or silica

  14. American Association for Clinical Chemistry

    MedlinePlus

    ... indispensable patient care tool. Learn more IN CLINICAL CHEMISTRY ddPCR Quantification of Lymphoma Mutations Researchers have developed ... Online Harmonization.net Commission on Accreditation in Clinical Chemistry American Board of Clinical Chemistry Clinical Chemistry Trainee ...

  15. Cell shape recognition by colloidal cell imprints: energy of the cell-imprint interaction.

    PubMed

    Borovička, Josef; Stoyanov, Simeon D; Paunov, Vesselin N

    2015-09-01

    The results presented in this study are aimed at the theoretical estimate of the interactions between a spherical microbial cell and the colloidal cell imprints in terms of the Derjaguin, Landau, Vervey, and Overbeek (DLVO) surface forces. We adapted the Derjaguin approximation to take into account the geometry factor in the colloidal interaction between a spherical target particle and a hemispherical shell at two different orientations with respect to each other. We took into account only classical DLVO surface forces, i.e., the van der Waals and the electric double layer forces, in the interaction of a spherical target cell and a hemispherical shell as a function of their size ratio, mutual orientation, distance between their surfaces, their respective surface potentials, and the ionic strength of the aqueous solution. We found that the calculated interaction energies are several orders higher when match and recognition between the target cell and the target cell imprint is achieved. Our analysis revealed that the recognition effect of the hemispherical shell towards the target microsphere comes from the greatly increased surface contact area when a full match of their size and shape is produced. When the interaction between the surfaces of the hemishell and the target cell is attractive, the recognition greatly amplifies the attraction and this increases the likelihood of them to bind strongly. However, if the surface interaction between the cell and the imprint is repulsive, the shape and size match makes this interaction even more repulsive and thus decreases the likelihood of binding. These results show that the surface chemistry of the target cells and their colloidal imprints is very important in controlling the outcome of the interaction, while the shape recognition only amplifies the interaction. In the case of nonmonotonous surface-to-surface interaction we discovered some interesting interplay between the effects of shape match and surface chemistry

  16. Cell shape recognition by colloidal cell imprints: Energy of the cell-imprint interaction

    NASA Astrophysics Data System (ADS)

    Borovička, Josef; Stoyanov, Simeon D.; Paunov, Vesselin N.

    2015-09-01

    The results presented in this study are aimed at the theoretical estimate of the interactions between a spherical microbial cell and the colloidal cell imprints in terms of the Derjaguin, Landau, Vervey, and Overbeek (DLVO) surface forces. We adapted the Derjaguin approximation to take into account the geometry factor in the colloidal interaction between a spherical target particle and a hemispherical shell at two different orientations with respect to each other. We took into account only classical DLVO surface forces, i.e., the van der Waals and the electric double layer forces, in the interaction of a spherical target cell and a hemispherical shell as a function of their size ratio, mutual orientation, distance between their surfaces, their respective surface potentials, and the ionic strength of the aqueous solution. We found that the calculated interaction energies are several orders higher when match and recognition between the target cell and the target cell imprint is achieved. Our analysis revealed that the recognition effect of the hemispherical shell towards the target microsphere comes from the greatly increased surface contact area when a full match of their size and shape is produced. When the interaction between the surfaces of the hemishell and the target cell is attractive, the recognition greatly amplifies the attraction and this increases the likelihood of them to bind strongly. However, if the surface interaction between the cell and the imprint is repulsive, the shape and size match makes this interaction even more repulsive and thus decreases the likelihood of binding. These results show that the surface chemistry of the target cells and their colloidal imprints is very important in controlling the outcome of the interaction, while the shape recognition only amplifies the interaction. In the case of nonmonotonous surface-to-surface interaction we discovered some interesting interplay between the effects of shape match and surface chemistry

  17. Fast microbial reduction of ferrihydrite colloids from a soil effluent

    NASA Astrophysics Data System (ADS)

    Fritzsche, Andreas; Bosch, Julian; Rennert, Thilo; Heister, Katja; Braunschweig, Juliane; Meckenstock, Rainer U.; Totsche, Kai U.

    2012-01-01

    Recent studies on the microbial reduction of synthetic iron oxide colloids showed their superior electron accepting property in comparison to bulk iron oxides. However, natural colloidal iron oxides differ in composition from their synthetic counterparts. Besides a potential effect of colloid size, microbial iron reduction may be accelerated by electron-shuttling dissolved organic matter (DOM) as well as slowed down by inhibitors such as arsenic. We examined the microbial reduction of OM- and arsenic-containing ferrihydrite colloids. Four effluent fractions were collected from a soil column experiment run under water-saturated conditions. Ferrihydrite colloids precipitated from the soil effluent and exhibited stable hydrodynamic diameters ranging from 281 (±146) nm in the effluent fraction that was collected first and 100 (±43) nm in a subsequently obtained effluent fraction. Aliquots of these oxic effluent fractions were added to anoxic low salt medium containing diluted suspensions of Geobacter sulfurreducens. Independent of the initial colloid size, the soil effluent ferrihydrite colloids were quickly and completely reduced. The rates of Fe2+ formation ranged between 1.9 and 3.3 fmol h-1 cell-1, and are in the range of or slightly exceeding previously reported rates of synthetic ferrihydrite colloids (1.3 fmol h-1 cell-1), but greatly exceeding previously known rates of macroaggregate-ferrihydrite reduction (0.07 fmol h-1 cell-1). The inhibition of microbial Fe(III) reduction by arsenic is unlikely or overridden by the concurrent enhancement induced by soil effluent DOM. These organic species may have increased the already high intrinsic reducibility of colloidal ferrihydrite owing to quinone-mediated electron shuttling. Additionally, OM, which is structurally associated with the soil effluent ferrihydrite colloids, may also contribute to the higher reactivity due to increasing solubility and specific surface area of ferrihydrite. In conclusion, ferrihydrite

  18. Physics of Colloids in Space (PCS): Microgravity Experiment Completed Operations on the International Space Station

    NASA Technical Reports Server (NTRS)

    Doherty, Michael P.; Sankaran, Subramanian

    2003-01-01

    Immediately after mixing, the two-phase-like colloid-polymer critical point sample begins to phase separate, or de-mix, into two phases-one that resembles a gas and one that resembles a liquid, except that the particles are colloids and not atoms. The colloid-poor black regions (colloidal gas) grow bigger, and the colloid-rich white regions (colloidal liquid) become whiter as the domains further coarsen. Finally, complete phase separation is achieved, that is, just one region of each colloid-rich (white) and colloid-poor (black) phase. This process was studied over four decades of length scale, from 1 micrometer to 1 centimeter.

  19. Colloidal Moderate-Refractive-Index Cu₂O Nanospheres as Visible-Region Nanoantennas with Electromagnetic Resonance and Directional Light-Scattering Properties.

    PubMed

    Zhang, Shouren; Jiang, Ruibin; Xie, Ya-Ming; Ruan, Qifeng; Yang, Baocheng; Wang, Jianfang; Lin, Hai-Qing

    2015-12-01

    Moderate-refractive-index dielectric nano-spheres are found to possess strong electric and magnetic dipole resonances in the visible region. Owing to the overlap of the electric and magnetic dipole resonances, moderate-refractive-index dielectric nanospheres exhibit directional forward scattering at the strongest scattering peak. Such directional scattering is experimentally observed on colloidal Cu2O nanospheres, which are readily prepared through wet-chemistry methods. PMID:26484637

  20. DNA hybridization and ligation for directed colloidal assembly

    NASA Astrophysics Data System (ADS)

    Shyr, Margaret

    Colloidal assembly using DNA hybridization has been pursued as a means assemble non-conventional ordered colloidal structures. However, to date it is undetermined whether DNA hybridization can be used to achieve non-FCC colloidal crystals. Using microcontact printing techniques, we have fabricated covalently bound single stranded DNA (ssDNA) two-dimensional arrays on glass surfaces, which were used to direct the assembly of complementary DNA functionalized polystyrene colloids. Two of the hallmarks of DNA hybridization, sequence specificity and thermal reversibility, were demonstrated. Due to the periodicity of these arrays, laser diffraction was used to directly monitor these structures during assembly. To demonstrate the versatility of the 2D colloidal array assembled via DNA hybridization, a catalytic DNA sequence or DNAzyme was incorporated into the colloidal array system. By tethering the enzymatic strand to the patterned glass surface and the substrate strand to polystyrene colloids, we showed that the DNAzyme could prevent the assembly of the arrays when the required Pb2+ cofactor was provided. Attempts to assemble the colloid arrays and disassemble via the Pb2+-DNAzyme induced cleavage were unsuccessful, likely due to the incomplete cleavage of the multitude of hybridized linkages between each colloid and the surface. Since DNA is not only capable of catalyzing reactions, but also capable of being reacted upon by a variety of biological enzymes, we examined the use of DNA ligase as a means to control the assembly of DNA-functionalized colloids. A three-sequence linker system was used for the hybridization mediated assembly of colloids: one sequence was tethered to the surface of the glass slide or colloids, one was tethered to another colloid surface, and the linker sequence hybridizes simultaneously to both tethered sequences. Once hybridized, the two tethered fragments can be ligated using DNA ligase, resulting in a continuous sequence tethered on one end

  1. Duration test of an annular colloid thruster.

    NASA Technical Reports Server (NTRS)

    Perel, J.; Mahoney, J. F.; Daley, H. L.

    1972-01-01

    An annular colloid thruster was continuously operated for 1023 hours. Performance was stable with no sparking and negligible drain currents observed. An average thrust of 25.1 micropounds and an average specific impulse of 1160 seconds were obtained at an accelerating voltage of 15 k he thruster exhaust beam was continuously neutralized using electrons and electrostatic vectoring was demonstrated periodically. The only clear trend with time was an increase in specific impulse during the last third of the test period. From these results the thruster lifetime was estimated to be over an order of magnitude greater than the test duration.

  2. Thermoelectricity and thermodiffusion in charged colloids

    NASA Astrophysics Data System (ADS)

    Huang, B. T.; Roger, M.; Bonetti, M.; Salez, T. J.; Wiertel-Gasquet, C.; Dubois, E.; Cabreira Gomes, R.; Demouchy, G.; Mériguet, G.; Peyre, V.; Kouyaté, M.; Filomeno, C. L.; Depeyrot, J.; Tourinho, F. A.; Perzynski, R.; Nakamae, S.

    2015-08-01

    The Seebeck and Soret coefficients of ionically stabilized suspension of maghemite nanoparticles in dimethyl sulfoxide are experimentally studied as a function of nanoparticle volume fraction. In the presence of a temperature gradient, the charged colloidal nanoparticles experience both thermal drift due to their interactions with the solvent and electric forces proportional to the internal thermoelectric field. The resulting thermodiffusion of nanoparticles is observed through forced Rayleigh scattering measurements, while the thermoelectric field is accessed through voltage measurements in a thermocell. Both techniques provide independent estimates of nanoparticle's entropy of transfer as high as 82 meV K-1. Such a property may be used to improve the thermoelectric coefficients in liquid thermocells.

  3. Colloidal solutions of organic conductive nanoparticles.

    PubMed

    de Caro, Dominique; Souque, Matthieu; Faulmann, Christophe; Coppel, Yannick; Valade, Lydie; Fraxedas, Jordi; Vendier, Olivier; Courtade, Frédéric

    2013-07-16

    Although molecular metals have been known for decades, their insolubility, low vapor pressure, and synthesis routes have prevented them from being integrated into electronic devices. We have prepared stable colloidal solutions of the organic metal TTF-TCNQ that overcome such difficulties. The solutions contain well-dispersed nanoparticles stabilized by long alkyl chain amines. They afford soluble powders by evaporation and homogeneous thin films by drop-casting. Powders and films show room temperature conductivities in the 0.01-0.1 S cm(-1) range. PMID:23772890

  4. Fractal-like structures in colloid science.

    PubMed

    Lazzari, S; Nicoud, L; Jaquet, B; Lattuada, M; Morbidelli, M

    2016-09-01

    The present work aims at reviewing our current understanding of fractal structures in the frame of colloid aggregation as well as the possibility they offer to produce novel structured materials. In particular, the existing techniques to measure and compute the fractal dimension df are critically discussed based on the cases of organic/inorganic particles and proteins. Then the aggregation conditions affecting df are thoroughly analyzed, pointing out the most recent literature findings and the limitations of our current understanding. Finally, the importance of the fractal dimension in applications is discussed along with possible directions for the production of new structured materials. PMID:27233526

  5. Crystalline Colloidal Arrays in Polymer Matrices

    NASA Technical Reports Server (NTRS)

    Sunkara, Hari B.; Penn, B. G.; Frazier, D. O.; Ramachandran, N.

    1997-01-01

    Crystalline Colloidal Arrays (CCA, also known as colloidal crystals), composed of aqueous or nonaqueous dispersions of self-assembled nanosized polymer colloidal spheres, are emerging toward the development of advanced optical devices for technological applications. The spontaneous self assembly of polymer spheres in a dielectric medium results from the electrostatic repulsive interaction between particles of uniform size and charge distribution. In a way similar to atomic crystals that diffract X-rays, CCA dispersions in thin quartz cells selectively and efficiently Bragg diffract the incident visible light. The reason for this diffraction is because the lattice (body or face centered cubic) spacing is on the order of the wavelength of visible light. Unlike the atomic crystals that diffract a fixed wavelength, colloidal crystals in principle, depending on the particle size, particle number and charge density, can diffract W, Vis or IR light. Therefore, the CCA dispersions can be used as laser filters. Besides, the diffraction intensity depends on the refractive index mismatch between polymer spheres and dielectric medium; therefore, it is possible to modulate incident light intensities by manipulating the index of either the spheres or the medium. Our interest in CCA is in the fabrication of all-optical devices such as optical switches, limiters, and spatial light modulators for optical signal processing. The two major requirements from a materials standpoint are the incorporation of suitable nonlinear optical materials (NLO) into polymer spheres which will allow us to alter the refractive index of the spheres by intense laser radiation, and preparation of solid CCA filters which can resist laser damage. The fabrication of solid composite filters not only has the advantage that the films are easier to handle, but also the arrays in solid films are more robust than in liquid media. In this paper, we report the photopolymerization process used to trap CCA in polymer

  6. Deterministic aggregation kinetics of superparamagnetic colloidal particles

    NASA Astrophysics Data System (ADS)

    Reynolds, Colin P.; Klop, Kira E.; Lavergne, François A.; Morrow, Sarah M.; Aarts, Dirk G. A. L.; Dullens, Roel P. A.

    2015-12-01

    We study the irreversible aggregation kinetics of superparamagnetic colloidal particles in two dimensions in the presence of an in-plane magnetic field at low packing fractions. Optical microscopy and image analysis techniques are used to follow the aggregation process and in particular study the packing fraction and field dependence of the mean cluster size. We compare these to the theoretically predicted scalings for diffusion limited and deterministic aggregation. It is shown that the aggregation kinetics for our experimental system is consistent with a deterministic mechanism, which thus shows that the contribution of diffusion is negligible.

  7. The promise of next generation colloids

    PubMed Central

    Creagh-Brown, Ben C; Evans, Timothy W

    2008-01-01

    The aim of perioperative haemodilution is to reduce loss of red blood cells during elective surgery. The oncotic and molecular characteristics of the various plasma substitutes employed determine how effectively normovolaemia is maintained, and their non-oncotic effects include alterations in microvascular perfusion. In the previous issue of Critical Care, Martini and colleagues assessed the effects of haemodilution with either polyethylene glycol (PEG)ylated albumin or a commercially available hydroxyethyl starch-based colloid in a hamster haemorrhage model. PEGylated albumin was superior to hydroxyethyl starch, as reflected by survival, haemodynamic parameters and assessment of the microcirculation using intravital microscopy. PMID:18492220

  8. Antibacterial Fluorinated Silica Colloid Superhydrophobic Surfaces

    PubMed Central

    Privett, Benjamin J.; Youn, Jonghae; Hong, Sung A; Lee, Jiyeon; Han, Junhee

    2011-01-01

    A superhydrophobic xerogel coating synthesized from a mixture of nanostructured fluorinated silica colloids, fluoroalkoxysilane, and a backbone silane is reported. The resulting fluorinated surface was characterized using contact angle goniometry, SEM, and AFM. Quantitative bacterial adhesion studies performed using a parallel plate flow cell demonstrated that the adhesion of Staphylococcus aureus and Pseudomonas aeruginosa were reduced by 2.08 ± 0.25 and 1.76 ± 0.12 log over controls, respectively. This simple superhydrophobic coating synthesis may be applied to any surface regardless of geometry and does not require harsh synthesis or processing conditions, making it an ideal candidate as a biopassivation strategy. PMID:21718023

  9. Colloidally deposited nanoparticle wires for biophysical detection

    NASA Astrophysics Data System (ADS)

    Shen, Sophie C.; Liu, Wen-Tao; Diao, Jia-Jie

    2015-12-01

    Among the techniques developed to prepare nanoparticle wires for multiple applications, the colloidal deposition method at interface has been regarded as cost-efficient and eco-friendly, and hence has attracted an increasing amount of research attention. In this report, the recent developments in preparing nanoparticle wires and integrated nanoparticle wire arrays using this technique have been reviewed. Furthermore, we have also discussed the application of these nanoparticle structures in detecting chemical and biological molecules. Project supported by the Fundamental Research Funds for the Central Universities through Xi’an Jiaotong University and the National Key Basic Research Program of China (Grant No. 2015CB856304).

  10. Lead removal with adsorbing colloid flotation

    SciTech Connect

    Thackston, E.L.; Wilson, D.J.; Hanson, J.S.; Miller, D.L. Jr.

    1980-02-01

    A process that removes lead from industrial waste by adsorbing colloid foam flotation has been designed and demonstrated. A system of ferric chloride and sodium lauryl sulfate, both relatively inexpensive chemicals, gave good performance with optimum dosages of sodium lauryl sulfate at 40 mg/l and trivalent iron at 150 mg/l. With optimum chemical and hydraulic conditions, the pilot plant was able to produce effluents with lead concentrations of less than 0.5 mg/l. The process may be especially attractive where space for heavy metals removal equipment is extremely limited.

  11. Stable monodisperse nanomagnetic colloidal suspensions: An overview.

    PubMed

    Ramimoghadam, Donya; Bagheri, Samira; Abd Hamid, Sharifah Bee

    2015-09-01

    Magnetic iron oxide nanoparticles (MNPs) have emerged as highly desirable nanomaterials in the context of many research works, due to their extensive industrial applications. However, they are prone to agglomerate on account of the anisotropic dipolar attraction, and therefore misled the particular properties related to single-domain magnetic nanostructures. The surface modification of MNPs is quite challenging for many applications, as it involves surfactant-coating for steric stability, or surface modifications that results in repulsive electrostatic force. Hereby, we focus on the dispersion of MNPs and colloidal stability. PMID:26073507

  12. Foam analogy in charged colloidal crystals.

    PubMed

    Kung, William; Ziherl, P; Kamien, Randall D

    2002-05-01

    We model charged colloidal suspensions using an analogy with foams. We study the solid-solid phase transitions of these systems as a function of particle volume fraction and ionic strength. The screened-Coulomb interaction is replaced by an interaction between walls of the Voronoi cells around each particle. We fit the surface charge to reproduce the phase diagram for the charged suspension studied by Sirota et al. [Phys. Rev. Lett. 62, 1524 (1989)]. With this fit parameter we are able to calculate the elastic moduli of the system and find good agreement with the available data. PMID:12059512

  13. Three-dimensional lock and key colloids.

    PubMed

    Wang, Yu; Wang, Yufeng; Zheng, Xiaolong; Yi, Gi-Ra; Sacanna, Stefano; Pine, David J; Weck, Marcus

    2014-05-14

    Colloids with well-defined multicavities are synthesized through the hydrolytic removal of silica cluster templates from organo-silica hybrid patchy particles. The geometry of the cavities stems from the originally assembled cluster templates, displaying well-defined three-dimensional symmetries, ranging from spherical, linear, triangular, tetrahedral, trigonal dipyramidal, octahedral, to pentagonal dipyramidal. The concave surface of the cavities is smooth, and the cavity shallowness and size can be varied. These particles with multicavities can act as "lock" particles with multiple "key holes". Up to n "key" particles can self-assemble into the lock particles via depletion interaction, resulting in multivalent, site-specific, reversible, and flexible bonding. PMID:24785203

  14. Steering trajectories in magnetically actuated colloidal propellers.

    PubMed

    Tierno, P; Sagués, F

    2012-08-01

    Microscale colloidal doublets composed of DNA-linked paramagnetic particles and floating close to a surface are able to propel in viscous fluids when subjected to external precessing magnetic fields. We show here that for certain values of the precession angle, the composite particles can be steered into tilted rather than linear trajectories characterized by a non-vanishing lateral velocity during motion. We extend the original model developed in Phys. Rev. Lett. 101, 218304 (2008) in order to explain this phenomenon, by including high-order corrections in the expansion of the director field and demonstrate the validity of this approach by comparing the analytical results with the experimental data. PMID:22872443

  15. Measurement of Diffraction Properties of Colloidal Crystals

    NASA Astrophysics Data System (ADS)

    Selan, Nicholas; Blades, Michael; Joy, Midhun; Gilchrist, James; Rotkin, Slava

    Close-packed, self-assembled arrays of micrometer polystyrene or silica spheres are high quality artificial crystals that generate well-defined diffraction patterns in the visible range. Such crystals are explored as possible substrates for deposition of nanomaterials such as graphene. Quasi-monochromatic visible light diffraction microscopy is used to characterize effective refractive index and crystal structure, specifically grain size, orientation, and lattice parameters. These parameters can be used to monitor deformations of the colloidal crystal lattice during transfer of nanomaterials. NSF ECCS-1509786, N.S. acknowledges RET supplement to NSF ECCS-1202398.

  16. Avalanches, plasticity, and ordering in colloidal crystals under compression

    NASA Astrophysics Data System (ADS)

    McDermott, D.; Reichhardt, C. J. Olson; Reichhardt, C.

    2016-06-01

    Using numerical simulations we examine colloids with a long-range Coulomb interaction confined in a two-dimensional trough potential undergoing dynamical compression. As the depth of the confining well is increased, the colloids move via elastic distortions interspersed with intermittent bursts or avalanches of plastic motion. In these avalanches, the colloids rearrange to minimize their colloid-colloid repulsive interaction energy by adopting an average lattice constant that is isotropic despite the anisotropic nature of the compression. The avalanches take the form of shear banding events that decrease or increase the structural order of the system. At larger compression, the avalanches are associated with a reduction of the number of rows of colloids that fit within the confining potential, and between avalanches the colloids can exhibit partially crystalline or anisotropic ordering. The colloid velocity distributions during the avalanches have a non-Gaussian form with power-law tails and exponents that are consistent with those found for the velocity distributions of gliding dislocations. We observe similar behavior when we subsequently decompress the system, and find a partially hysteretic response reflecting the irreversibility of the plastic events.

  17. Avalanches, plasticity, and ordering in colloidal crystals under compression.

    PubMed

    McDermott, D; Reichhardt, C J Olson; Reichhardt, C

    2016-06-01

    Using numerical simulations we examine colloids with a long-range Coulomb interaction confined in a two-dimensional trough potential undergoing dynamical compression. As the depth of the confining well is increased, the colloids move via elastic distortions interspersed with intermittent bursts or avalanches of plastic motion. In these avalanches, the colloids rearrange to minimize their colloid-colloid repulsive interaction energy by adopting an average lattice constant that is isotropic despite the anisotropic nature of the compression. The avalanches take the form of shear banding events that decrease or increase the structural order of the system. At larger compression, the avalanches are associated with a reduction of the number of rows of colloids that fit within the confining potential, and between avalanches the colloids can exhibit partially crystalline or anisotropic ordering. The colloid velocity distributions during the avalanches have a non-Gaussian form with power-law tails and exponents that are consistent with those found for the velocity distributions of gliding dislocations. We observe similar behavior when we subsequently decompress the system, and find a partially hysteretic response reflecting the irreversibility of the plastic events. PMID:27415320

  18. Recent Results from the Physics of Colloids in Space

    NASA Technical Reports Server (NTRS)

    Weitz, David A.; Bailey, A.; Christianson, R.; Manley, S.; Prasad, V.; Segre, P.; Gasser, U.; Cipelletti, L.; Schoefield, A.; Pusey, P.

    2002-01-01

    The Physics of Colloids in Space is an experiment which flew in the ISS. Data on several different samples of colloidal particles were obtained. They provided unexpected information about the behavior of the samples in microgravity. The data are currently being analyzed. The most recent findings will be discussed in this talk.

  19. Feasibility of colloidal silver SERS for rapid bacterial screening

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Citrate-reduced silver colloids have been used extensively for surface-enhanced Raman scattering (SERS) study and are commonly characterized by UV-visible spectroscopy. In this work, relative standard deviation (RSD) of SERS spectra from silver colloidal suspensions and ratios of SERS peaks from sma...

  20. Fabrication and Characterization of Colloidal Crystal Thin Films

    ERIC Educational Resources Information Center

    Rodriguez, I.; Ramiro-Manzano, F.; Meseguer, F.; Bonet, E.

    2011-01-01

    We present a laboratory experiment that allows undergraduate or graduate students to get introduced to colloidal crystal research concepts in an interesting way. Moreover, such experiments and studies can also be useful in the field of crystallography or solid-state physics. The work concerns the growth of colloidal crystal thin films obtained…

  1. Stable Colloidal Drug Aggregates Catch and Release Active Enzymes.

    PubMed

    McLaughlin, Christopher K; Duan, Da; Ganesh, Ahil N; Torosyan, Hayarpi; Shoichet, Brian K; Shoichet, Molly S

    2016-04-15

    Small molecule aggregates are considered nuisance compounds in drug discovery, but their unusual properties as colloids could be exploited to form stable vehicles to preserve protein activity. We investigated the coaggregation of seven molecules chosen because they had been previously intensely studied as colloidal aggregators, coformulating them with bis-azo dyes. The coformulation reduced colloid sizes to <100 nm and improved uniformity of the particle size distribution. The new colloid formulations are more stable than previous aggregator particles. Specifically, coaggregation of Congo Red with sorafenib, tetraiodophenolphthalein (TIPT), or vemurafenib produced particles that are stable in solutions of high ionic strength and high protein concentrations. Like traditional, single compound colloidal aggregates, the stabilized colloids adsorbed and inhibited enzymes like β-lactamase, malate dehydrogenase, and trypsin. Unlike traditional aggregates, the coformulated colloid-protein particles could be centrifuged and resuspended multiple times, and from resuspended particles, active trypsin could be released up to 72 h after adsorption. Unexpectedly, the stable colloidal formulations can sequester, stabilize, and isolate enzymes by spin-down, resuspension, and release. PMID:26741163

  2. A Stochastic Model for Colloid Transport and Deposition

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Profiles of retained colloids in porous media have frequently been observed to be hyper-exponential or nonmonotonic with transport depth under unfavorable attachment conditions, whereas filtration theory predicts an exponential profile. In this work we present a stochastic model for colloid transpo...

  3. Colloidal deposition and aggregation in the presence of charged collectors

    NASA Astrophysics Data System (ADS)

    Sadri, Behnam; Rajendran, Arvind; Bhattacharjee, Subir; Colloids; complex fluid laboratory Team

    2014-11-01

    The transport of colloidal particles in porous media is of great importance in sub-surface environments. These colloidal particles facilitate transport of contaminants, low-soluble compounds and metals in groundwater. Here, we have studied transport dynamics of colloids inside porous medium using a combination of column experiments and batch studies. Polystyrene latex beads (100 nm), as colloidal agents, and soda lime glass beads, as porous medium, are employed in this work. On the one hand, batch experiments are undertaken to better understand concurrent aggregation and deposition of particles. On the other hand, column experiments are performed to understand the flow induced deposition of colloidal particles in the interstitial voids. Effect of collector surface preparation, pH, colloidal suspension concentration and collector beads mass is studied. Chemical release and shear field are revealed as two significant factors lying behind the coagulation of colloidal particles. These findings help us to better distinguish mechanisms responsible for the transport of colloids inside porous medium. We are collaborators. Behnam Sadri is master of science student while two other professor are supervising his research work.

  4. Reentrant phase transitions from depletion: colloidal crystals to flocculation

    NASA Astrophysics Data System (ADS)

    Feng, Lang; Laderman, Bezia; Sacanna, Stefano; Chaikin, Paul

    2014-03-01

    Conventional depletion is supposed to be temperature independent. However, we find that many typical colloid-depletion systems show remarkable phenomena as temperature is varied. 1 μm polystyrene spheres in water are known to form colloidal crystals when PEO is added as a depletant. When this system is heated the crystal melts at a first critical temperature T1 ~ 60 C , and then at higher temperature T2 ~ 70 C the colloids flocculate. We argue that a weak temperature-dependent interaction between polymer and colloid is responsible for the observed phenomena: crystals form when the colloid-polymer interaction is repulsive, flocculation occurs when the interaction is attractive, and melting occurs in between when both phases are frustrated. The melted phase occurs due to an unexpected cancelation when combining both entropic and enthalpic attractions. We propose a simple statistical model to map out the observed transitions and fill the theoretical gap between the two established scenarios for colloid-polymer systems, namely depletion and flocculation. We have seen the same temperature dependent phenomena for TPM, PS and silica spheres with PEO and dextran as depletants. Our discovery provides a fundamental understanding of the polymer-colloid system and opens new possibilities for colloidal self-assembly and temperature-controlled viscoelastic materials.

  5. STABILITY AND TRANSPORT OF INORGANIC COLLOIDS THROUGH CONTAMINATED AQUIFER MATERIAL

    EPA Science Inventory

    Laboratory columns using contaminated natural aquifer material from Globe, Arizona, were used to investigate the transport of inorganic colloids under saturated flow conditions. e2O3 radio-labeled spherical colloids of various diameters were synthesized and introduced into the co...

  6. Physics of Colloids in Space: Flight Hardware Operations on ISS

    NASA Technical Reports Server (NTRS)

    Doherty, Michael P.; Bailey, Arthur E.; Jankovsky, Amy L.; Lorik, Tibor

    2002-01-01

    The Physics of Colloids in Space (PCS) experiment was launched on Space Shuttle STS-100 in April 2001 and integrated into EXpedite the PRocess of Experiments to Space Station Rack 2 on the International Space Station (ISS). This microgravity fluid physics investigation is being conducted in the ISS U.S. Lab 'Destiny' Module over a period of approximately thirteen months during the ISS assembly period from flight 6A through flight 9A. PCS is gathering data on the basic physical properties of simple colloidal suspensions by studying the structures that form. A colloid is a micron or submicron particle, be it solid, liquid, or gas. A colloidal suspension consists of these fine particles suspended in another medium. Common colloidal suspensions include paints, milk, salad dressings, cosmetics, and aerosols. Though these products are routinely produced and used, we still have much to learn about their behavior as well as the underlying properties of colloids in general. The long-term goal of the PCS investigation is to learn how to steer the growth of colloidal structures to create new materials. This experiment is the first part of a two-stage investigation conceived by Professor David Weitz of Harvard University (the Principal Investigator) along with Professor Peter Pusey of the University of Edinburgh (the Co-Investigator). This paper describes the flight hardware, experiment operations, and initial science findings of the first fluid physics payload to be conducted on ISS: The Physics of Colloids in Space.

  7. Spontaneous resolution of a colloid cyst of the third ventricle.

    PubMed

    Annamalai, G; Lindsay, K W; Bhattacharya, J J

    2008-01-01

    We report a case of an asymptomatic colloid cyst of the third ventricle in a 35-year-old male, which on follow-up MRI at 15 months appears to have spontaneously resolved. To our knowledge, this is the first such case reported and supports the role of conservative management of small asymptomatic colloid cysts. PMID:18079347

  8. Colloid adhesive parameters for chemical heterogeneous porous media

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A simple modeling approach was developed to calculate colloid adhesive parameters for chemically heterogeneous porous media. The area of the zone of electrostatic influence between a colloid and solid-water interface (Az) was discretized into a number of equally sized grid cells to capture chemical...

  9. Coherent Acoustic Phonons in Colloidal Semiconductor Nanocrystal Superlattices.

    PubMed

    Poyser, Caroline L; Czerniuk, Thomas; Akimov, Andrey; Diroll, Benjamin T; Gaulding, E Ashley; Salasyuk, Alexey S; Kent, Anthony J; Yakovlev, Dmitri R; Bayer, Manfred; Murray, Christopher B

    2016-01-26

    The phonon properties of films fabricated from colloidal semiconductor nanocrystals play a major role in thermal conductance and electron scattering, which govern the principles for building colloidal-based electronics and optics including thermoelectric devices with a high ZT factor. The key point in understanding the phonon properties is to obtain the strength of the elastic bonds formed by organic ligands connecting the individual nanocrystallites. In the case of very weak bonding, the ligands become the bottleneck for phonon transport between infinitively rigid nanocrystals. In the opposite case of strong bonding, the colloids cannot be considered as infinitively rigid beads and the distortion of the superlattice caused by phonons includes the distortion of the colloids themselves. We use the picosecond acoustics technique to study the acoustic coherent phonons in superlattices of nanometer crystalline CdSe colloids. We observe the quantization of phonons with frequencies up to 30 GHz. The frequencies of quantized phonons depend on the thickness of the colloidal films and possess linear phonon dispersion. The measured speed of sound and corresponding wave modulus in the colloidal films point on the strong elastic coupling provided by organic ligands between colloidal nanocrystals. PMID:26696021

  10. Assembling patchy nanorods with spheres: limitations imposed by colloidal interactions

    NASA Astrophysics Data System (ADS)

    Pothorszky, Sz.; Zámbó, D.; Deák, T.; Deák, A.

    2016-02-01

    For gold nanorods the intrinsic shape-anisotropy offers the prospect of anisotropic assembly, provided that their region-selective surface modification can be realized. Here we developed nanorods with a patchy surface chemistry, featuring positively charged molecules in the tip region and polymer molecules at the sides by careful control of molecule concentrations during ligand exchange. When these patchy nanorods are assembled with small negatively charged spherical particles, electric double layer interaction can direct the assembly of two nanospheres at the opposite ends of the nanorods. The PEG chains promote the selectivity of the procedure. As the size of the nanospheres increases, they start to shift towards the side of the nanorod due to increased van der Waals interaction. When the relative size of the nanospheres is even larger, only a single nanosphere is assembled, but instead of the tip region, they are attached to the side of the nanorods. The apparent cross-over of the region-selectivity can be interpreted in terms of colloidal interactions, i.e. the second spherical particle is excluded due to nanosphere-nanosphere electric double layer repulsion, while the large vdW attraction results in a side positioning of the single adsorbed spherical particle. The results underline the importance of absolute values of the different interaction strengths and length scales in the programmed assembly of patchy nanoscale building blocks.For gold nanorods the intrinsic shape-anisotropy offers the prospect of anisotropic assembly, provided that their region-selective surface modification can be realized. Here we developed nanorods with a patchy surface chemistry, featuring positively charged molecules in the tip region and polymer molecules at the sides by careful control of molecule concentrations during ligand exchange. When these patchy nanorods are assembled with small negatively charged spherical particles, electric double layer interaction can direct the

  11. Predicting colloid transport through saturated porous media: A critical review

    NASA Astrophysics Data System (ADS)

    Molnar, Ian L.; Johnson, William P.; Gerhard, Jason I.; Willson, Clinton S.; O'Carroll, Denis M.

    2015-09-01

    Understanding and predicting colloid transport and retention in water-saturated porous media is important for the protection of human and ecological health. Early applications of colloid transport research before the 1990s included the removal of pathogens in granular drinking water filters. Since then, interest has expanded significantly to include such areas as source zone protection of drinking water systems and injection of nanometals for contaminated site remediation. This review summarizes predictive tools for colloid transport from the pore to field scales. First, we review experimental breakthrough and retention of colloids under favorable and unfavorable colloid/collector interactions (i.e., no significant and significant colloid-surface repulsion, respectively). Second, we review the continuum-scale modeling strategies used to describe observed transport behavior. Third, we review the following two components of colloid filtration theory: (i) mechanistic force/torque balance models of pore-scale colloid trajectories and (ii) approximating correlation equations used to predict colloid retention. The successes and limitations of these approaches for favorable conditions are summarized, as are recent developments to predict colloid retention under the unfavorable conditions particularly relevant to environmental applications. Fourth, we summarize the influences of physical and chemical heterogeneities on colloid transport and avenues for their prediction. Fifth, we review the upscaling of mechanistic model results to rate constants for use in continuum models of colloid behavior at the column and field scales. Overall, this paper clarifies the foundation for existing knowledge of colloid transport and retention, features recent advances in the field, critically assesses where existing approaches are successful and the limits of their application, and highlights outstanding challenges and future research opportunities. These challenges and opportunities

  12. Humic colloid-borne natural polyvalent metal ions: dissociation experiment.

    PubMed

    Geckeis, H; Rabung, Th; Ngo Manh, T; Kim, J I; Beck, H P

    2002-07-01

    The natural association nature of the humic colloid-borne trace elements is investigated. Rare earth elements (REE) Th and U are chosen as naturally occurring representatives and chemical homologues for actinides of different oxidation states present in nuclear waste. Tri- and tetravalent elements in two investigated Gorleben groundwaters (Gohy-532 and -2227) almost exclusively occur as humic or fulvic colloid-borne species. Their desorption behavior from colloids is examined in the unperturbed groundwater (pH approximately 8) under anaerobic conditions (Ar/1% CO2) by addition of a chelating cation exchanger resin. Particularly, the dissociation process of naturally occurring Eu(III) in the groundwater is compared with the Eu(III) desorption from its humate complex prepared with purified Aldrich humic acid in a buffered aqueous solution at pH approximately 8. The Eu(III) dissociation from the groundwater colloids is found to be considerably slower than found for the humate complex synthesized in the laboratory. This suggests that under natural aquatic conditions the Eu(III) binding in colloids is chemically different from the simple humate complexation as observed in the laboratory experiment. The colloid characterization bythe size exclusion chromatography (SEC) and the flow field-flow fractionation (FFFF) indicates that natural colloid-borne trace elements are found predominantly in colloids of larger size (>15 nm in size), while Eu(III) in its humate complex is found mainly in colloids of hydrodynamic diameters <5 nm. The slower desorption kinetics and the larger colloid size suggest that the polyvalent metal ion binding in natural humic colloids is associated to polynucleation with other co-present trace metal ions. Radiotracer experiments reveal that isotopic equilibria with the naturally colloid-borne trace elements are not attained within a period of more than 100 days, indicating irreversible binding of at least a part of colloid-borne polyvalent trace

  13. Dielectric effects on the ion distribution near a Janus colloid

    NASA Astrophysics Data System (ADS)

    Wu, Huanxin; Han, Ming; Luijten, Erik

    Spherical Janus colloids, particles with two domains of different materials, are typically heterogeneous in permittivity. This dielectric heterogeneity will influence their behavior in electrolytes, ranging from their aggregation to their electrokinetics in external fields. We investigate the structure of the electric double layer around spherical Janus colloids immersed in solution via molecular dynamics simulations. Polarization of the colloidal surfaces by the surrounding ions is calculated dynamically with a boundary-element method based Poisson solver. One observation is that even neutral Janus colloids may carry a net dipole moment in the presence of asymmetric salts. Moreover, we extend this study to incorporate a spatially varying permittivity of the solvent near a charged Janus colloid, and demonstrate the effect of this dielectric variation on the electric double layer.

  14. SUBSURFACE MOBILE PLUTONIUM SPECIATION: SAMPLING ARTIFACTS FOR GROUNDWATER COLLOIDS

    SciTech Connect

    Kaplan, D.; Buesseler, K.

    2010-06-29

    A recent review found several conflicting conclusions regarding colloid-facilitated transport of radionuclides in groundwater and noted that colloids can both facilitate and retard transport. Given these contrasting conclusions and the profound implications even trace concentrations of plutonium (Pu) have on the calculated risk posed to human health, it is important that the methodology used to sample groundwater colloids be free of artifacts. The objective of this study was: (1) to conduct a field study and measure Pu speciation, ({sup 239}Pu and {sup 240}Pu for reduced-Pu{sub aq}, oxidized-Pu{sub aq}, reduced-Pu{sub colloid}, and oxidized-Pu{sub colloid}), in a Savannah River Site (SRS) aquifer along a pH gradient in F-Area, (2) to determine the impact of pumping rate on Pu concentration, Pu speciation, and Pu isotopic ratios, (3) determine the impact of delayed sample processing (as opposed to processing directly from the well).

  15. Using depletion to control colloidal crystal assemblies of hard cuboctahedra.

    PubMed

    Karas, Andrew S; Glaser, Jens; Glotzer, Sharon C

    2016-06-21

    Depletion interactions arise from entropic forces, and their ability to induce aggregation and even ordering of colloidal particles through self-assembly is well established, especially for spherical colloids. We vary the size and concentration of penetrable hard sphere depletants in a system of cuboctahedra, and we show how depletion changes the preferential facet alignment of the colloids and thereby selects different crystal structures. Moreover, we explain the cuboctahedra phase behavior using perturbative free energy calculations. We find that cuboctahedra can form a stable simple cubic phase, and, remarkably, that the stability of this phase can be rationalized only by considering the effects of both the colloid and depletant entropy. We corroborate our results by analyzing how the depletant concentration and size affect the emergent directional entropic forces and hence the effective particle shape. We propose the use of depletants as a means of easily changing the effective shape of self-assembling anisotropic colloids. PMID:27194463

  16. Reconfigurable multi-scale colloidal assembly on excluded volume patterns

    NASA Astrophysics Data System (ADS)

    Edwards, Tara D.; Yang, Yuguang; Everett, W. Neil; Bevan, Michael A.

    2015-09-01

    The ability to create multi-scale, periodic colloidal assemblies with unique properties is important to emerging applications. Dynamically manipulating colloidal structures via tunable kT-scale attraction can provide the opportunity to create particle-based nano- and microstructured materials that are reconfigurable. Here, we report a novel tactic to obtain reconfigurable, multi-scale, periodic colloidal assemblies by combining thermoresponsive depletant particles and patterned topographical features that, together, reversibly mediate local kT-scale depletion interactions. This method is demonstrated in optical microscopy experiments to produce colloidal microstructures that reconfigure between well-defined ordered structures and disordered fluid states as a function of temperature and pattern feature depth. These results are well described by Monte Carlo simulations using theoretical depletion potentials that include patterned excluded volume. Ultimately, the approach reported here can be extended to control the size, shape, orientation, and microstructure of colloidal assemblies on multiple lengths scales and on arbitrary pre-defined pattern templates.

  17. Laser speckle reduction via colloidal-dispersion-filled projection screens.

    PubMed

    Riechert, Falko; Bastian, Georg; Lemmer, Uli

    2009-07-01

    We use projection screens filled with colloidal dispersions to reduce laser speckle in laser projection systems. Laser light is multiply scattered at the globules of the colloidal dispersion's internal phase, which do Brownian movement. The integration time of the human eye causes a perception of a reduced laser speckle contrast because of temporal averaging. As a counteracting effect, blurring of projected images occurs in the colloidal dispersion, which degrades image quality. We measure and compare speckle reduction and blurring of three different colloidal dispersions filled into transmission screens of different thicknesses. We realized a high speckle contrast reduction at simultaneously low blurring with a thin screen filled with a highly scattering colloidal dispersion with forward-peaked scattering. We realize speckle contrast values below 3% at acceptable blurring. PMID:19571932

  18. Nonlinear machine learning and design of reconfigurable digital colloids.

    PubMed

    Long, Andrew W; Phillips, Carolyn L; Jankowksi, Eric; Ferguson, Andrew L

    2016-09-14

    Digital colloids, a cluster of freely rotating "halo" particles tethered to the surface of a central particle, were recently proposed as ultra-high density memory elements for information storage. Rational design of these digital colloids for memory storage applications requires a quantitative understanding of the thermodynamic and kinetic stability of the configurational states within which information is stored. We apply nonlinear machine learning to Brownian dynamics simulations of these digital colloids to extract the low-dimensional intrinsic manifold governing digital colloid morphology, thermodynamics, and kinetics. By modulating the relative size ratio between halo particles and central particles, we investigate the size-dependent configurational stability and transition kinetics for the 2-state tetrahedral (N = 4) and 30-state octahedral (N = 6) digital colloids. We demonstrate the use of this framework to guide the rational design of a memory storage element to hold a block of text that trades off the competing design criteria of memory addressability and volatility. PMID:27498992

  19. Glassy dislocation dynamics in colloidal dimer crystals

    NASA Astrophysics Data System (ADS)

    Gerbode, Sharon

    2012-02-01

    Dislocation mobility is central to both the mechanical response and the relaxation mechanisms of crystalline materials. Recent experiments have explored the role of novel particle anisotropies in affecting the rules of defect motion in crystals. ``Peanut-shaped'' colloidal dimer particles consisting of two connected spherical lobes form densely packed crystals in 2D. In these ``degenerate crystals,'' the particle lobes occupy triangular lattice sites while the particle axes are randomly oriented among the three crystalline directions. One consequence of the random orientations of the dimers is that dislocation glide is severely limited by certain particle arrangements in the degenerate crystals. Using optical tweezers to manipulate single lobe-sized spherical intruder particles, we locally deform the crystal, creating defects. During subsequent relaxation, the dislocations formed during the deformation leave the crystal grain, either via annihilation with other dislocations or by moving to a grain boundary. Interestingly, in large crystalline grains this dislocation relaxation occurs through a two-stage process reminiscent of slow relaxations in glassy systems, suggesting the novel concept that glassy phenomena may be introduced to certain kinds of colloidal crystals via simple anisotropic constituents.

  20. Critical Casimir forces for colloidal assembly.

    PubMed

    Nguyen, V D; Dang, M T; Nguyen, T A; Schall, P

    2016-02-01

    Critical Casimir forces attract increasing interest due to their opportunities for reversible particle assembly in soft matter and nano science. These forces provide a thermodynamic analogue of the celebrated quantum mechanical Casimir force that arises from the confinement of vacuum fluctuations of the electromagnetic field. In its thermodynamic analogue, solvent fluctuations, confined between suspended particles, give rise to an attractive or repulsive force between the particles. Due to its unique temperature dependence, this effect allows in situ control of reversible assembly. Both the force magnitude and range vary with the solvent correlation length in a universal manner, adjusting with temperature from fractions of the thermal energy, k B T, and nanometre range to several ten kT and micrometer length scale. Combined with recent breakthroughs in the synthesis of complex particles, critical Casimir forces promise the design and assembly of complex colloidal structures, for fundamental studies of equilibrium and out-of-equilibrium phase behaviour. This review highlights recent developments in this evolving field, with special emphasis on the dynamic interaction control to assemble colloidal structures, in and out of equilibrium. PMID:26750980