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Sample records for adv colloid interface

  1. 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.

  2. Colloids at Curved Fluid Interfaces

    NASA Astrophysics Data System (ADS)

    Stebe, Kathleen

    2016-11-01

    Fluid interfaces are remarkable sites for colloidal assembly. When a colloid attaches to a fluid interface, it distorts a region around it; this distortion has an associated capillary energy, the product of its area and interfacial tension. The particle's capillary energy depends on the local interface curvature. By molding the interface, we can define curvature fields that drive microparticles along pre-determined paths. This example captures the emergent nature of the interactions. We discuss curvature fields as analogues to external electro-magnetic fields, and define curvatures that drive particles to well-defined locations, and to equilibrium sites far from boundaries. Particle-particle and particle-curvature interactions can guide particles into structures via interaction among many particles. This work demonstrates the potential importance of curvature capillary interactions in schemes to make reconfigurable materials, since interfaces and their associated capillary energy landscapes can be readily reconfigured. Analogies in other soft systems will be described. Support acknowledged from NSF DMR 1607878.

  3. 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.

  4. Nonequilibrium interfaces in colloidal fluids

    NASA Astrophysics Data System (ADS)

    Bier, Markus; Arnold, Daniel

    2013-12-01

    The time-dependent structure, interfacial tension, and evaporation of an oversaturated colloid-rich (liquid) phase in contact with an undersaturated colloid-poor (vapor) phase of a colloidal dispersion is investigated theoretically during the early-stage relaxation, where the interface is relaxing towards a local equilibrium state while the bulk phases are still out of equilibrium. Since systems of this type exhibit a clear separation of colloidal and solvent relaxation time scales with typical times of interfacial tension measurements in between, they can be expected to be suitable for analogous experimental studies, too. The major finding is that, irrespective of how much the bulk phases differ from two-phase coexistence, the interfacial structure and the interfacial tension approach those at two-phase coexistence during the early-stage relaxation process. This is a surprising observation since it implies that the relaxation towards global equilibrium of the interface is not following but preceding that of the bulk phases. Scaling forms for the local chemical potential, the flux, and the dissipation rate exhibit qualitatively different leading order contributions depending on whether an equilibrium or a nonequilibrium system is considered. The degree of nonquilibrium between the bulk phases is found to not influence the qualitative relaxation behavior (i.e., the values of power-law exponents), but to determine the quantitative deviation of the observed quantities from their values at two-phase coexistence. Whereas the underlying dynamics differs between colloidal and molecular fluids, the behavior of quantities such as the interfacial tension approaching the equilibrium values during the early-stage relaxation process, during which nonequilibrium conditions of the bulk phases are not changed, can be expected to occur for both types of systems.

  5. Tissue Boundaries: Mimicking Tissue Boundaries by Sharp Multiparameter Matrix Interfaces (Adv. Healthcare Mater. 15/2016).

    PubMed

    Sapudom, Jiranuwat; Rubner, Stefan; Martin, Steve; Pompe, Tilo

    2016-08-01

    Engineering interfaces of extracellular compartments mimicking native tissues is key to study cell behavior in a physiologically relevant context and for a successful translation of these new biomaterials engineering principles in regenerative and therapeutic applications. Tilo Pompe and co-workers demonstrate a strategy to engineer multiparameter matrix interfaces using a sequential reconstitution of two well-defined Collagen I based matrices on page 1861. Such matrix interfaces trigger cell migration directionality normal to the interface plane in dependence on matrix pore size.

  6. Does colloid shape affect detachment of colloids by a moving air-water interface?

    PubMed

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

    2013-05-14

    Air-water interfaces interact strongly with colloidal particles by capillary forces. The magnitude of the interaction force depends on, among other things, the particle shape. Here, we investigate the effects of particle shape on colloid detachment by a moving air-water interface. We used hydrophilic polystyrene colloids with four different shapes (spheres, barrels, rods, and oblong disks), but otherwise identical surface properties. The nonspherical shapes were created by stretching spherical microspheres on a film of polyvinyl alcohol (PVA). The colloids were then deposited onto the inner surface of a glass channel. An air bubble was introduced into the channel and passed through, thereby generating a receding followed by an advancing air-water interface. The detachment of colloids by the air-water interfaces was visualized with a confocal microscope, quantified by image analysis, and analyzed statistically to determine significant differences. For all colloid shapes, the advancing air-water interface caused pronounced colloid detachment (>63%), whereas the receding interface was ineffective in colloid detachment (<1.5%). Among the different colloid shapes, the barrels were most readily removed (94%) by the advancing interface, followed by the spheres and oblong disks (80%) and the rods (63%). Colloid detachment was significantly affected by colloid shape. The presence of an edge, as it occurs in a barrel-shaped colloid, promoted colloid detachment because the air-water interface is being pinned at the edge of the colloid. This suggests that the magnitude of colloid mobilization and transport in porous media is underestimated for edged particles and overestimated for rodlike particles when a sphere is used as a model colloid.

  7. Liquid-vapor interfaces of patchy colloids

    NASA Astrophysics Data System (ADS)

    Oleksy, A.; Teixeira, P. I. C.

    2015-01-01

    We investigate the liquid-vapor interface of a model of patchy colloids. This model consists of hard spheres decorated with short-ranged attractive sites ("patches") of different types on their surfaces. We focus on a one-component fluid with two patches of type A and nine patches of type B (2 A 9 B colloids), which has been found to exhibit reentrant liquid-vapor coexistence curves and very low-density liquid phases. We have used the density-functional theory form of Wertheim's first-order perturbation theory of association, as implemented by Yu and Wu [J. Chem. Phys. 116, 7094 (2002), 10.1063/1.1463435], to calculate the surface tension, and the density and degree of association profiles, at the liquid-vapor interface of our model. In reentrant systems, where A B bonds dominate, an unusual thickening of the interface is observed at low temperatures. Furthermore, the surface tension versus temperature curve reaches a maximum, in agreement with Bernardino and Telo da Gama's mesoscopic Landau-Safran theory [Phys. Rev. Lett. 109, 116103 (2012), 10.1103/PhysRevLett.109.116103]. If B B attractions are also present, competition between A B and B B bonds gradually restores the monotonic temperature dependence of the surface tension. Lastly, the interface is "hairy," i.e., it contains a region where the average chain length is close to that in the bulk liquid, but where the density is that of the vapor. Sufficiently strong B B attractions remove these features, and the system reverts to the behavior seen in atomic fluids.

  8. Tuning Colloid-Interface Interactions by Salt Partitioning

    NASA Astrophysics Data System (ADS)

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

    2016-08-01

    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.

  9. Electrostatic interaction between colloidal particles trapped at an electrolyte interface.

    PubMed

    Majee, Arghya; Bier, Markus; Dietrich, S

    2014-04-28

    The electrostatic interaction between colloidal particles trapped at the interface between two immiscible electrolyte solutions is studied in the limit of small inter-particle distances. Within an appropriate model analytic expressions for the electrostatic potential as well as for the surface and line interaction energies are obtained. They demonstrate that the widely used superposition approximation, which is commonly applied to large distances between the colloidal particles, fails qualitatively at small distances, and is quantitatively unreliable even at large distances. Our results contribute to an improved description of the interaction between colloidal particles trapped at fluid interfaces.

  10. Charge-Controlled Colloids on Liquid-Liquid Interfaces

    NASA Astrophysics Data System (ADS)

    Kunz, Daniel A.; Reck, Bernd; Manoharan, Vinothan N.

    2014-03-01

    The tendency of colloidal particles to stabilize interfaces has been exploited for many years to generate Pickering emulsions with a variety of industrial applications. However, the exact stabilization mechanism and its dependence on the surface properties of the colloidal particles are not yet fully understood. We provide new interfacial studies on the nonequilibrium dynamics of a colloidal system with tunable surface charge density. We push individual sub-micron colloidal particles towards an oil-water interface and track their motion in three-dimensions using holographic microscopy to examine the influence of zeta potential on the dynamics of the system. This project was funded by the BASF Advanced Research Initiative, BASF SE, Germany.

  11. Non-capillary binding of colloidal particles to liquid interfaces

    NASA Astrophysics Data System (ADS)

    Kaz, David; McGorty, Ryan; Manoharan, Vinothan

    2012-02-01

    We observe colloidal polystyrene particles binding reversibly to an oil-water interface through the combination of a repulsive electrostatic force and an attractive van der Waals force. Previously studied interactions of an aqueous colloidal particle and a liquid interface have generally fallen into two categories: 1) electrostatic repulsion indicated by the dependence on salt and 2) capillary adsorption where surface tension brings the particle in contact with both phases and is indicated by practically irreversible binding. With our technique of pushing individual colloidal particles towards a planar oil-water interface and observing their motion in three-dimensions with holographic microscopy we have observed both interactions. However, our observations indicate that under certain conditions the electrostatic repulsion, which is due to repulsive image charges, is weak enough for a particle to experience a van der Waals attraction while strong enough to prevent a particle from penetrating the interface and becoming bound through capillary action. We observe individual particles transition between repulsive and attractive interactions with the interface suggesting that these colloidal particles have a heterogeneous surface charge.

  12. Ultrafast desorption of colloidal particles from fluid interfaces

    PubMed Central

    Poulichet, Vincent; Garbin, Valeria

    2015-01-01

    The self-assembly of solid particles at fluid–fluid interfaces is widely exploited to stabilize emulsions and foams, and in materials synthesis. The self-assembly mechanism is very robust owing to the large capillary energy associated with particle adsorption, of the order of millions of times the thermal energy for micrometer-sized colloids. The microstructure of the interfacial colloid monolayer can also favor stability, for instance in the case of particle-stabilized bubbles, which can be indefinitely stable against dissolution due to jamming of the colloid monolayer. As a result, significant challenges arise when destabilization and particle removal are a requirement. Here we demonstrate ultrafast desorption of colloid monolayers from the interface of particle-stabilized bubbles. We drive the bubbles into periodic compression–expansion using ultrasound waves, causing significant deformation and microstructural changes in the particle monolayer. Using high-speed microscopy we uncover different particle expulsion scenarios depending on the mode of bubble deformation, including highly directional patterns of particle release during shape oscillations. Complete removal of colloid monolayers from bubbles is achieved in under a millisecond. Our method should find a broad range of applications, from nanoparticle recycling in sustainable processes to programmable particle delivery in lab-on-a-chip applications. PMID:25922529

  13. Ultrafast desorption of colloidal particles from fluid interfaces.

    PubMed

    Poulichet, Vincent; Garbin, Valeria

    2015-05-12

    The self-assembly of solid particles at fluid-fluid interfaces is widely exploited to stabilize emulsions and foams, and in materials synthesis. The self-assembly mechanism is very robust owing to the large capillary energy associated with particle adsorption, of the order of millions of times the thermal energy for micrometer-sized colloids. The microstructure of the interfacial colloid monolayer can also favor stability, for instance in the case of particle-stabilized bubbles, which can be indefinitely stable against dissolution due to jamming of the colloid monolayer. As a result, significant challenges arise when destabilization and particle removal are a requirement. Here we demonstrate ultrafast desorption of colloid monolayers from the interface of particle-stabilized bubbles. We drive the bubbles into periodic compression-expansion using ultrasound waves, causing significant deformation and microstructural changes in the particle monolayer. Using high-speed microscopy we uncover different particle expulsion scenarios depending on the mode of bubble deformation, including highly directional patterns of particle release during shape oscillations. Complete removal of colloid monolayers from bubbles is achieved in under a millisecond. Our method should find a broad range of applications, from nanoparticle recycling in sustainable processes to programmable particle delivery in lab-on-a-chip applications.

  14. Detachment of colloids from a solid surface by a moving air-water interface.

    PubMed

    Sharma, Prabhakar; Flury, Markus; Zhou, Jun

    2008-10-01

    Colloid attachment to liquid-gas interfaces is an important process used in industrial applications to separate suspended colloids from the fluid phase. Moving gas bubbles can also be used to remove colloidal dust from surfaces. Similarly, moving liquid-gas interfaces lead to colloid mobilization in the natural subsurface environment, such as in soils and sediments. The objective of this study was to quantify the effect of moving air-water interfaces on the detachment of colloids deposited on an air-dried glass surface, as a function of colloidal properties and interface velocity. We selected four types of polystyrene colloids (positive and negative surface charge, hydrophilic and hydrophobic). The colloids were deposited on clean microscope glass slides using a flow-through deposition chamber. Air-water interfaces were passed over the colloid-deposited glass slides, and we varied the number of passages and the interface velocity. The amounts of colloids deposited on the glass slides were visualized using confocal laser scanning microscopy and quantified by image analysis. Our results showed that colloids attached under unfavorable conditions were removed in significantly greater amounts than those attached under favorable conditions. Hydrophobic colloids were detached more than hydrophilic colloids. The effect of the air-water interface on colloid removal was most pronounced for the first two passages of the air-water interface. Subsequent passages of air-water interfaces over the colloid-deposited glass slides did not cause significant additional colloid removal. Increasing interface velocity led to decreased colloid removal. The force balances, calculated from theory, supported the experimental findings, and highlight the dominance of detachment forces (surface tension forces) over the attachment forces (DLVO forces).

  15. The Importance of Moving Air-Water Interfaces for Colloid Transport in Porous Media

    NASA Astrophysics Data System (ADS)

    Flury, M.

    2015-12-01

    In the vadose zone, or in unsaturated porous media in general, transport of colloids is usually less pronounced than in groundwater. An important retention mechanism for colloids in unsaturated porous media is attachment to air-water interfaces. However, air-water interfaces can also lead to colloid mobilization and enhanced transport if air-water interfaces are moving, such as during infiltration, imbibition, and drainage. Colloid attachment to air-water interfaces is caused by surface tension forces, and these forces usually exceed other interactions forces; therefore, surface tension forces play a dominant role for colloid transport in unsaturated porous media. In this presentation, experimental and theoretical evidence of surface tension forces acting on colloids will be presented, and the role of moving air-water interfaces will be discussed.

  16. Adsorption dynamics of colloidal ellipsoids at oil-water interfaces

    NASA Astrophysics Data System (ADS)

    Wang, Anna; Rogers, W. Benjamin; Manoharan, Vinothan N.

    Nonspherical particles at immiscible fluid interfaces have strong interactions with each other and with the curvature of the host interface. However, the dynamics of nonspherical colloidal particles attaching to an interface have not yet been studied. We use digital holographic microscopy to image micron-sized polystyrene ellipsoids breaching an oil-water interface at hundreds of frames per second. We show that the particle height and polar angle have large fluctuations, but both change approximately logarithmic with time, likely due to contact line pinning on the surface of the particle. Equilibrium is reached on a timescale at least three orders of magnitude slower than that expected from Langevin dynamics simulations. We also find that all the trajectories collapse into straight lines when we plot particle polar angle as a function of particle height, unlike the trajectories seen in simulation. The differences between experiment and simulation suggest that contact line pinning and the shape of the three phase contact line may strongly influence the dynamics of particle adsorption.

  17. Phase behavior of charged colloids at a fluid interface

    NASA Astrophysics Data System (ADS)

    Kelleher, Colm P.; Guerra, Rodrigo E.; Hollingsworth, Andrew D.; Chaikin, Paul M.

    2017-02-01

    We study the phase behavior of a system of charged colloidal particles that are electrostatically bound to an almost flat interface between two fluids. We show that, despite the fact that our experimental system consists of only 103-104 particles, the phase behavior is consistent with the theory of melting due to Kosterlitz, Thouless, Halperin, Nelson, and Young. Using spatial and temporal correlations of the bond-orientational order parameter, we classify our samples into solid, isotropic fluid, and hexatic phases. We demonstrate that the topological defect structure we observe in each phase corresponds to the predictions of Kosterlitz-Thouless-Halperin-Nelson-Young theory. By measuring the dynamic Lindemann parameter γL(τ ) and the non-Gaussian parameter α2(τ ) of the displacements of the particles relative to their neighbors, we show that each of the phases displays distinctive dynamical behavior.

  18. Interaction of Charged Colloidal Particles at the Air-Water Interface.

    PubMed

    Girotto, Matheus; Dos Santos, Alexandre P; Levin, Yan

    2016-07-07

    We study, using Monte Carlo simulations, the interaction between charged colloidal particles confined to the air-water interface. The dependence of force on ionic strength and counterion valence is explored. For 1:1 electrolyte, we find that the electrostatic interaction at the interface is very close to the one observed in the bulk. On the other hand, for salts with multivalent counterions, an interface produces an enhanced attraction between like charged colloids. Finally, we explore the effect of induced surface charge at the air-water interface on the interaction between colloidal particles.

  19. Fabrication of colloidal photonic crystal heterostructures free of interface imperfection based on solvent vapor annealing.

    PubMed

    Liu, Xiaomiao; Zhao, Duobiao; Geng, Chong; Zhang, Lijing; Tan, Tianya; Hu, Mingzhe; Yan, Qingfeng

    2014-11-15

    We describe the transformation of a colloidal photonic crystal into a photonic crystal heterostructure. It was achieved by annealing a polystyrene multilayer colloidal photonic crystal partially immersed in water using a solvent vapor. The floating polystyrene colloidal photonic crystal was divided into two parts by the liquid level, which can be manipulated by the addition of ethanol into the water. The top part protruding out of the water experienced a uniform lattice stretching upon exposure to the solvent vapor. The bottom part that stayed immersed in the water remained unaffected due to the protection by the water. The inconsistent behaviors of the two parts resulted in the formation of a colloidal photonic crystal heterostructure. Such a heterostructure was free of interface imperfection since it was a direct descendant of the original colloidal crystal. Meanwhile, optical measurements demonstrated the presence of a wider photonic band gap along the crystallographic [111] direction in these photonic crystal heterostructures compared with the original colloidal photonic crystals.

  20. Interface instability modes in freezing colloidal suspensions: revealed from onset of planar instability

    PubMed Central

    Wang, Lilin; You, Jiaxue; Wang, Zhijun; Wang, Jincheng; Lin, Xin

    2016-01-01

    Freezing colloidal suspensions widely exists in nature and industry. Interface instability has attracted much attention for the understandings of the pattern formation in freezing colloidal suspensions. However, the interface instability modes, the origin of the ice banding or ice lamellae, are still unclear. In-situ experimental observation of the onset of interface instability remains absent up to now. Here, by directly imaging the initial transient stage of planar interface instability in directional freezing colloidal suspensions, we proposed three interface instability modes, Mullins-Sekerka instability, global split instability and local split instability. The intrinsic mechanism of the instability modes comes from the competition of the solute boundary layer and the particle boundary layer, which only can be revealed from the initial transient stage of planar instability in directional freezing. PMID:26996630

  1. Effective interaction between a colloid and a soft interface near criticality.

    PubMed

    Law, A D; Harnau, L; Tröndle, M; Dietrich, S

    2014-10-07

    Within mean-field theory we determine the universal scaling function for the effective force acting on a single colloid located near the interface between two coexisting liquid phases of a binary liquid mixture close to its critical consolute point. This is the first study of critical Casimir forces emerging from the confinement of a fluctuating medium by at least one shape responsive, soft interface, instead of by rigid walls only as studied previously. For this specific system, our semi-analytical calculation illustrates that knowledge of the colloid-induced, deformed shape of the interface allows one to accurately describe the effective interaction potential between the colloid and the interface. Moreover, our analysis demonstrates that the critical Casimir force involving a deformable interface is accurately described by a universal scaling function, the shape of which differs from that one for rigid walls.

  2. Physical ageing of the contact line on colloidal particles at liquid interfaces.

    PubMed

    Kaz, David M; McGorty, Ryan; Mani, Madhav; Brenner, Michael P; Manoharan, Vinothan N

    2011-12-04

    Young's law predicts that a colloidal sphere in equilibrium with a liquid interface will straddle the two fluids, its height above the interface defined by an equilibrium contact angle. This has been used to explain why colloids often bind to liquid interfaces, and has been exploited in emulsification, water purification, mineral recovery, encapsulation and the making of nanostructured materials. However, little is known about the dynamics of binding. Here we show that the adsorption of polystyrene microspheres to a water/oil interface is characterized by a sudden breach and an unexpectedly slow relaxation. The relaxation appears logarithmic in time, indicating that complete equilibration may take months. Surprisingly, viscous dissipation appears to play little role. Instead, the observed dynamics, which bear strong resemblance to ageing in glassy systems, agree well with a model describing activated hopping of the contact line over nanoscale surface heterogeneities. These results may provide clues to longstanding questions on colloidal interactions at an interface.

  3. Effective interaction between a colloid and a soft interface near criticality

    SciTech Connect

    Law, A. D. Harnau, L. Tröndle, M. Dietrich, S.

    2014-10-07

    Within mean-field theory we determine the universal scaling function for the effective force acting on a single colloid located near the interface between two coexisting liquid phases of a binary liquid mixture close to its critical consolute point. This is the first study of critical Casimir forces emerging from the confinement of a fluctuating medium by at least one shape responsive, soft interface, instead of by rigid walls only as studied previously. For this specific system, our semi-analytical calculation illustrates that knowledge of the colloid-induced, deformed shape of the interface allows one to accurately describe the effective interaction potential between the colloid and the interface. Moreover, our analysis demonstrates that the critical Casimir force involving a deformable interface is accurately described by a universal scaling function, the shape of which differs from that one for rigid walls.

  4. Dynamic broadening of the crystal-fluid interface of colloidal hard spheres.

    PubMed

    Dullens, Roel P A; Aarts, Dirk G A L; Kegel, Willem K

    2006-12-01

    We investigate the structure and dynamics of the crystal-fluid interface of colloidal hard spheres in real space by confocal microscopy. Tuning the buoyancy of the particles allows us to study the interface close to and away from equilibrium. We find that the interface broadens from 8-9 particle diameters close to equilibrium to 15 particle diameters away from equilibrium. Furthermore, the interfacial velocity, i.e., the velocity by which the interface moves upwards, increases significantly. The increasing gravitational drive leads to supersaturation of the fluid above the crystal surface. This dramatically affects crystal nucleation and growth, resulting in the observed dynamic broadening of the crystal-fluid interface.

  5. Structure and Spectroscopy of Buried Interfaces in Organic Thin Films and Colloids

    DTIC Science & Technology

    2012-03-01

    interfaces of micron to nanometer size particles buried deep in colloids. We have shown for the first time that SHG from the surface of silver ...patent application on Metallic Nanoparticles with Saturated Coverage of Thiols for Greatly Enhancing Fluorescence Yield is in preparation and will be...bonding. The interface dipole of the benzene- silver complex have been determined to be 5.41.8 D. For aniline on Ag(111) there is repulsive inter

  6. Capillarity-induced ordering of spherical colloids on an interface with anisotropic curvature.

    PubMed

    Ershov, Dmitry; Sprakel, Joris; Appel, Jeroen; Cohen Stuart, Martien A; van der Gucht, Jasper

    2013-06-04

    Objects floating at a liquid interface, such as breakfast cereals floating in a bowl of milk or bubbles at the surface of a soft drink, clump together as a result of capillary attraction. This attraction arises from deformation of the liquid interface due to gravitational forces; these deformations cause excess surface area that can be reduced if the particles move closer together. For micrometer-sized colloids, however, the gravitational force is too small to produce significant interfacial deformations, so capillary forces between spherical colloids at a flat interface are negligible. Here, we show that this is different when the confining liquid interface has a finite curvature that is also anisotropic. In that case, the condition of constant contact angle along the three-phase contact line can only be satisfied when the interface is deformed. We present experiments and numerical calculations that demonstrate how this leads to quadrupolar capillary interactions between the particles, giving rise to organization into regular square lattices. We demonstrate that the strength of the governing anisotropic interactions can be rescaled with the deviatoric curvature alone, irrespective of the exact shape of the liquid interface. Our results suggest that anisotropic interactions can easily be induced between isotropic colloids through tailoring of the interfacial curvature.

  7. Stability and minimum size of colloidal clusters on a liquid-air interface

    NASA Astrophysics Data System (ADS)

    Pergamenshchik, V. M.

    2012-02-01

    A vertical force applied to each of two colloids, trapped at a liquid-air interface, induces their logarithmic pairwise attraction. I recently showed [Phys. Rev. EPLEEE81539-375510.1103/PhysRevE.79.011407 79, 011407 (2009)] that in clusters of size R much larger than the capillary length λ, the attraction changes to that of a power law and is much stronger due to a many-body effect, and I derived two equations that describe the equilibrium coarse-grained meniscus profile and colloid density in such clusters. In this paper, this theory is shown also to describe small clusters with R≪ λ provided the number N of colloids therein is sufficiently large. An analytical solution for a small circular cluster with an arbitrary short-range power-law pairwise repulsion is found. The energy of a cluster is obtained as a function of its radius R and colloid number N. As in large clusters, the attraction force and energy universally scale with the distance L between colloids as L-3 and L-2, respectively, for any repulsion forces. The states of an equilibrium cluster, predicted by the theory, are shown to be stable with respect to small perturbations of the meniscus profile and colloid density. The minimum number of colloids in a circular cluster, which sustains the thermal motion, is estimated. For standard parameters, it can be very modest, e.g., in the range 20-200, which is in line with experimental findings on reversible clusterization on a liquid-air interface.

  8. Dynamics of non-spherical colloidal particles near and at oil-water interfaces

    NASA Astrophysics Data System (ADS)

    Wang, Anna; Dimiduk, Thomas G.; Fung, Jerome; Chaudhary, Kundan; Lewis, Jennifer A.; Razavi, Sepideh; Kretzschmar, Ilona; Manoharan, Vinothan N.

    2014-03-01

    Whereas much is known about how spherical colloidal particles interact with and at oil-water interfaces, not much is known about their non-spherical counterparts. The rotation of non-spherically symmetric particles adds extra degrees of freedom to how such particles interact with each other and the interface, so to study their three-dimensional dynamics we must first be able to image the rotation which has so far only been possible in viscous fluids or for particles with large aspect ratios. Here we track both the three-dimensional translation and the rotation of non-spherical colloidal particles at high speeds using the discrete dipole approximation in conjunction with digital holographic microscopy. We study the dynamics of such particles at an oil-water interface to determine interactions and dynamics prior to or after attachment. We aim to connect these measurements to the formation and stability of Pickering emulsions.

  9. Active colloids at liquid-liquid interfaces: dynamic self-assembly and functionality

    NASA Astrophysics Data System (ADS)

    Snezhko, Alexey; Aranson, Igor

    2012-02-01

    Self-assembled materials must actively consume energy and remain out of equilibrium in order to support structural complexity and functional diversity. Colloids of interacting particles suspended at liquid-liquid interfaces and maintained out of equilibrium by external alternating electromagnetic fields develop nontrivial collective dynamics and self-assembly. We use ferromagnetic colloidal micro-particles (so the magnetic moment is fixed in each particle and interactions between colloids is highly anisotropic and directional) suspended over an interface of two immiscible liquids and energized by vertical alternating magnetic fields to demonstrate novel dynamic and active self-assembled structures (``asters'') which are not accessible through thermodynamic assembly. Structures are attributed to the interplay between surface waves, generated at the liquid/liquid interface by the collective response of magnetic microparticles to the alternating magnetic field, and hydrodynamic fields induced in the boundary layers of both liquids forming the interface. Two types of magnetic order are reported. We demonstrate that asters develop self-propulsion in the presence of a small in-plane dc magnetic field. We show that asters can capture, transport, and position target microparticles.

  10. Cosmology in a petri dish? Simulation of collective of colloids at fluid interfaces

    NASA Astrophysics Data System (ADS)

    Bleibel, J.

    2014-04-01

    Interfacially trapped, micrometer-sized colloidal particles interact via ranged capillary attraction which is analogous to two-dimensional screened Newtonian gravity with the capillary length λ as the tuneable screening length. Using Brownian namics simulations and density functional theory, we study the dynamics of an initially prepared distribution of colloids, either a random homogeneous distribution, or a finitely- sized patch of colloids. Whereas the limit λ → ∞ corresponds to the global collapse self-gravitating fluid, for smaller λ the dynamics crosses over to spinodal decomposition showing a coarsening of regions of enhanced density which emerge from initial fluctuations. For the finite patch of colloids and intermediate λ we predict theoretically and serve in simulations a ringlike density peak at the outer rim of the disclike patch, moving as an inbound shock wave. Experimental realizations of this crossover scenario appear be well possible for colloids trapped at water interfaces and having a radius of around micrometer. Finally, the influence of hydrodynamic interactions on this capillary collapse will be discussed briefly.

  11. Polystyrene colloidal crystals: Interface controlled thermal conductivity in an open-porous mesoparticle superstructure.

    PubMed

    Nutz, Fabian A; Ruckdeschel, Pia; Retsch, Markus

    2015-11-01

    Colloidal crystals typically consist of sub-micron sized monodisperse particles, which are densely packed on a face centered cubic lattice. While many properties of this material class have been studied over the past decades, little is known about their thermal transport properties. The high amount of interfaces and their small interparticle contact area should result in efficient thermal insulation. Using laser flash analysis we report for the first time on the temperature dependent thermal conductivity of a freestanding 366 nm polystyrene (PS) colloidal crystal. Macroscopic monoliths of these samples were fabricated by colloidal self-assembly. We demonstrate a very low thermal conductivity κ of 51 mW K(-1) m(-1) (κ of bulk PS∼140 mW K(-1) m(-1)). Remarkably, this low thermal conductivity is reached at a comparatively high density of 750 kg m(-3). It can be further increased by almost 300% upon film formation and loss of the colloidal mesostructure. Additionally, this open porous structure is largely independent of the surrounding atmosphere. This can be rationalized by the small size (∼100 nm) of the pores present within this colloidal crystal.

  12. Correlated Diffusion of Colloidal Particles near a Liquid-Liquid Interface

    PubMed Central

    Zhang, Wei; Chen, Song; Li, Na; Zhang, Jia zheng; Chen, Wei

    2014-01-01

    Optical microscopy and multi-particle tracking are used to investigate the cross-correlated diffusion of quasi two-dimensional colloidal particles near an oil-water interface. The behaviors of the correlated diffusion along longitudinal and transverse direction are asymmetric. It is shown that the characteristic length for longitudinal and transverse correlated diffusion are particle diameter and the distance from particle center to the interface, respectively, for large particle separation . The longitudinal and transverse correlated diffusion coefficient and are independent of the colloidal area fraction when , which indicates that the hydrodynamic interactions(HIs) among the particles are dominated by HIs through the surrounding fluid for small . For high area fraction , the power law exponent for the spatial decay of begins to decrease, which suggests the HIs are more contributed from the 2D particle monolayer self for large . PMID:24465498

  13. Emulsions stabilised by food colloid particles: role of particle adsorption and wettability at the liquid interface.

    PubMed

    Paunov, Vesselin N; Cayre, Olivier J; Noble, Paul F; Stoyanov, Simeon D; Velikov, Krassimir P; Golding, Matt

    2007-08-15

    We study the effect of the particle wettability on the preferred type of emulsion stabilised solely by food colloid particles. We present results obtained with the recently developed gel trapping technique (GTT) for characterisation of wettability and surface structuring of individual food colloid particles adsorbed at air-water and oil-water interfaces. This method allows us to replicate a particle monolayer onto the surface of polydimethylsiloxane (PDMS) without altering the position of the particles. By observing the polymer surface with scanning electron microscopy (SEM), we are able to determine the contact angle of the individual particles at the initial liquid interface. We demonstrate that the GTT can be applied to fat crystal particles, calcium carbonate particles coated with stearic acid and spray-dried soy protein/calcium phosphate particles at air-water and oil-water interfaces. Subsequently, we prepare emulsions of decane and water stabilised by the same food colloid particles and correlate the wettability data obtained for these particles to the preferred type of emulsions they stabilise.

  14. Colloidal binary mixtures at fluid-fluid interfaces under steady shear: structural, dynamical and mechanical response†

    PubMed Central

    Zell, Zachary A.; Squires, Todd M.; Isa, Lucio

    2015-01-01

    We experimentally study the link between structure, dynamics and mechanical response of two-dimensional (2D) binary mixtures of colloidal microparticles spread at water/oil interfaces. The particles are driven into steady shear by a microdisk forced to rotate at a controlled angular velocity. The flow causes particles to layer into alternating concentric rings of small and big colloids. The formation of such layers is linked to the local, position-dependent shear rate, which triggers two distinct dynamical regimes: particles either move continuously (“Flowing”) close to the microdisk, or exhibit intermittent “Hopping” between local energy minima farther away. The shear-rate-dependent surface viscosity of the monolayers can be extracted from a local interfacial stress balance, giving “macroscopic” flow curves whose behavior corresponds to the distinct microscopic regimes of particle motion. Hopping Regions reveal a higher resistance to flow compared to the Flowing Regions, where spatial organization into layers reduces dissipation. PMID:26347409

  15. Effect of interaction heterogeneity on colloidal arrangements at a curved oil-water interface.

    PubMed

    Lee, Mina; Lee, Daeyeon; Park, Bum Jun

    2015-01-14

    We report the unique arrangement behaviour of colloidal particles at a curved oil-water interface. Particles trapped at a centrosymmetrically curved oil-water interface, formed by placing an oil lens at a neat air-water interface, organize into diverse arrangement structures due to electrostatic repulsion under the gravitational field. To reveal a possible mechanism behind the observed diversity, we investigate the interactions between pairs of particles at the curved oil-water interface. The magnitude of electrostatic repulsive interactions between pairs of particles is determined by minimizing the total potential of the particle pairs. We show that the pair interactions are quite heterogeneous, following a Gamma distribution. Using the experimentally determined pair potential and the heterogeneity in the potential as input parameters for Monte Carlo simulations, we show that such interaction heterogeneity affects the particle arrangements at the curved interface and results in an observed diversity in the particle arrangement structures. We believe that this work prompts further experimental and simulation studies to extensively understand hierarchical relations from small scale measurements (e.g., pair interactions and heterogeneity) to bulk scale properties (e.g., microstructure and interfacial rheology).

  16. Interaction between colloidal particles on an oil-water interface in dilute and dense phases.

    PubMed

    Parolini, Lucia; Law, Adam D; Maestro, Armando; Buzza, D Martin A; Cicuta, Pietro

    2015-05-20

    The interaction between micron-sized charged colloidal particles at polar/non-polar liquid interfaces remains surprisingly poorly understood for a relatively simple physical chemistry system. By measuring the pair correlation function g(r) for different densities of polystyrene particles at the decane-water interface, and using a powerful predictor-corrector inversion scheme, effective pair-interaction potentials can be obtained up to fairly high densities, and these reproduce the experimental g(r) in forward simulations, so are self consistent. While at low densities these potentials agree with published dipole-dipole repulsion, measured by various methods, an apparent density dependence and long range attraction are obtained when the density is higher. This condition is thus explored in an alternative fashion, measuring the local mobility of colloids when confined by their neighbors. This method of extracting interaction potentials gives results that are consistent with dipolar repulsion throughout the concentration range, with the same magnitude as in the dilute limit. We are unable to rule out the density dependence based on the experimental accuracy of our data, but we show that incomplete equilibration of the experimental system, which would be possible despite long waiting times due to the very strong repulsions, is a possible cause of artefacts in the inverted potentials. We conclude that to within the precision of these measurements, the dilute pair potential remains valid at high density in this system.

  17. Electrohydrodynamic controlled assembly and fracturing of thin colloidal particle films confined at drop interfaces

    NASA Astrophysics Data System (ADS)

    Rozynek, Z.; Dommersnes, P.; Mikkelsen, A.; Michels, L.; Fossum, J. O.

    2014-09-01

    Particles can adsorb strongly at liquid interfaces due to capillary forces, which in practice can confine the particles to the interface. Here we investigate the electrohydrodynamic flow driven packing and deformation of colloidal particle layers confined at the surface of liquid drops. The electrohydrodynamic flow has a stagnation point at the drop equator, leading to assembly of particles in a ribbon shaped film. The flow is entirely controlled by the electric field, and we demonstrate that AC fields can be used to induce hydrodynamic "shaking" of the colloidal particle film. We find that the mechanical properties of the film is highly dependent on the particles: monodisperse polystyrene beads form packed granular monolayers which "liquefies" upon shaking, whereas clay mineral particles form cohesive films that fracture upon shaking. The results are expected to be relevant for understanding the mechanics and rheology of particle stabilized emulsions. Supplementary material in the form of a pdf file available from the Journal web page at http://dx.doi.org/10.1140/epjst/e2014-02231-x

  18. Directed Self-assembly of Colloidal Particles on a Blue Phase I Interface

    NASA Astrophysics Data System (ADS)

    Martinez-Gonzalez, Jose; Zhou, Ye; Sadati, Monirosadat; Abbott, Nicholas; de Pablo, Juan

    Blue phases are liquid states of matter with a highly ordered defect structure which confers unique properties among complex fluids. In this work, a free energy model of chiral liquid crystals is used to consider the self-assembly of colloids and nanoparticles on the interface of a Blue Phase I. It is shown that the crystalline defect structure of the blue phase produces intricate, two-dimensional hexagonal and Kagome structures among the nanoparticle arrangements, with lattice parameters that depend on the type of anchoring of the liquid crystal at the particle's surface. These parameters can be tuned via the chirality of the material, thereby offering intriguing possibilities for the creation of hierarchical materials based on the directed assembly of particles in chiral liquid crystals. This work is supported by the Department of Energy, Basic Energy Sciences, Materials Science and Engineering Division, Biomaterials Program, through DE-SC004025.

  19. 75 FR 49233 - Amendments to Form ADV

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-12

    ... From the Federal Register Online via the Government Publishing Office ] Part III Securities and... / Vol. 75 , No. 155 / Thursday, August 12, 2010 / Rules and Regulations#0;#0; ] SECURITIES AND EXCHANGE COMMISSION 17 CFR Parts 275 and 279 RIN 3235-AI17 Amendments to Form ADV AGENCY: Securities and...

  20. Generation and stability of bentonite colloids at the bentonite/granite interface of a deep geological radioactive waste repository.

    PubMed

    Missana, Tiziana; Alonso, Ursula; Turrero, Maria Jesús

    2003-03-01

    The possible mechanisms of colloid generation at the near field/far field interface of a radioactive repository have been investigated by means of novel column experiments simulating the granite/bentonite boundary, both in dynamic and in quasi-static water flow conditions. It has been shown that solid particles and colloids can be detached from the bulk and mobilised by the water flow. The higher the flow rate, the higher the concentration of particles found in the water, according to an erosion process. However, the gel formation and the intrinsic tactoid structure of the clay play an important role in the submicron particle generation even in the compacted clay and in a confined system. In fact, once a bentonite gel is formed, in the regions where the clay is contacted with water, clay colloids can be formed even in quasi-static flow conditions. The potential relevance of these colloids in radionuclide transport has been studied by evaluating their stability in different chemical environments. The coagulation kinetics of natural bentonite colloids was experimentally studied as a function of the ionic strength and pH, by means of time-resolved light scattering techniques. It has been shown that these colloids are very stable in low saline (approximately 1 x 10(-3) M) and alkaline (pH > or = 8) waters.

  1. Introducing high-quality planar defects into colloidal crystals via self-assembly at the air/water interface

    NASA Astrophysics Data System (ADS)

    Zhong, Kuo; Demeyer, Pieter-Jan; Zhou, Xingping; Kruglova, Olga; Verellen, Niels; Moshchalkov, Victor V.; Song, Kai; Clays, Koen

    2015-02-01

    We demonstrate a facile method for fabrication of colloidal crystals containing a planar defect by using PS@SiO2 core-shell spheres as building blocks. A monolayer of solid spheres was embedded in core-shell colloidal crystals serving as the defect layer, which formed by means of self-assembly at the air/water interface. Compared with previous methods, this fabrication method results in pronounced passbands in the band gaps of the colloidal photonic crystal. The FWHM of the obtained passband is only ~16nm, which is narrower than the previously reported results. The influence of the defect layer thickness on the optical properties of these sandwiched structures was also investigated. No high-cost processes or specific equipment is needed in our approach. Inverse opals with planar defects can be obtained via calcination of the PS cores, without the need of infiltration. The experimental results are in good agreement with simulations performed using the FDTD method.

  2. Nanoscale Interfaces in Colloidal Quantum Dot Solar Cells: Physical Insights and Materials Engineering Strategies

    NASA Astrophysics Data System (ADS)

    Kemp, Kyle Wayne

    With growing global energy demand there will be an increased need for sources of renewable energy such as solar cells. To make these photovoltaic technologies more competitive with conventional energy sources such as coal and natural gas requires further reduction in manufacturing costs that can be realized by solution processing and roll-to-roll printing. Colloidal quantum dots are a bandgap tunable, solution processible, semiconductor material which may offer a path forward to efficient, inexpensive photovoltaics. Despite impressive progress in performance with these materials, there remain limitations in photocarrier collection that must be overcome. This dissertation focuses on the characterization of charge recombination and transport in colloidal quantum dot photovoltaics, and the application of this knowledge to the development of new and better materials. Core-shell, PbS-CdS, quantum dots were investigated in an attempt to achieve better surface passivation and reduce electronic defects which can limit performance. Optimization of this material led to improved open circuit voltage, exceeding 0.6 V for the first time, and record published performance of 6% efficiency. Using temperature-dependent and transient photovoltage measurements we explored the significance of interface recombination on the operation of these devices. Careful engineering of the electrode using atomic layer deposition of ZnO helped lead to better TiO2 substrate materials and allowed us to realize a nearly two-fold reduction in recombination rate and an enhancement upwards of 50 mV in open circuit voltage. Carrier extraction efficiency was studied in these devices using intensity dependent current-voltage data of an operational solar cell. By developing an analytical model to describe recombination loss within the active layer of the device we were able to accurately determine transport lengths ranging up to 90 nm. Transient absorption and photoconductivity techniques were used to study

  3. Structuring of colloidal particles at interfaces and the relationship to food emulsion and foam stability.

    PubMed

    Dickinson, Eric

    2015-07-01

    We consider the influence of spherical colloidal particles on the structure and stabilization of dispersions, emulsions and foams. Emphasis is placed on developments in the use of the methods of liquid state theory and computer simulation to understand short-range structuring of concentrated colloidal dispersions and ordering of particle layers near surfaces and within liquid films. Experimental information on the structuring of surfactant micelles and caseinate particles in thin liquid films is described, including an assessment of the effect of particle polydispersity on depletion interactions and kinetic structural stabilization. We specifically discuss the relevance of some of these structural concepts to the stability of food colloids.

  4. Long-range attraction between colloidal spheres at the air-water interface: the consequence of an irregular meniscus

    PubMed

    Stamou; Duschl; Johannsmann

    2000-10-01

    Recent observations of charged colloidal particles trapped at the air-water interface revealed long-range interparticle attractive forces, not accounted for by the standard theories of colloidal interactions. We propose a mechanism for attraction which is based on nonuniform wetting causing an irregular shape of the particle meniscus. The excess water surface area created by these distortions can be minimized when two adjacent particles assume an optimum relative orientation and distance. Typically, for spheres with diameter of 1 &mgr;m at an interparticle distance of 2 &mgr;m, deviations from the ideal contact line by as little as 50 nm result in an interaction energy of the order of 10(4)kT. Roughness-induced capillarity explains the experimental findings, including the cluster dissolution caused by addition of detergent to the subphase and the formation of linear aggregates. This kind of interaction should also be of importance in particle-stabilized foams and emulsions.

  5. Controlling the Transient Interface Shape and Deposition Profile Left by Desiccation of Colloidal Droplets on Multiple Polymer Surfaces

    NASA Astrophysics Data System (ADS)

    Dunning, Peter David

    A colloidal suspension is a small constituent of insoluble solid particles suspended in a liquid medium. Control over the wetting, evaporation, and deposition patterns left by colloidal suspensions is valuable in many biological, medical, industrial, and agricultural applications. Understanding the governing principles of wetting and evaporative phenomena of these colloidal suspensions may lead to greater control over resultant deposition patterns. Perhaps the most familiar pattern forms when an initially heterogeneous colloidal suspension leaves a dark ring pattern at the edge of a drop. This pattern is referred to as a coffee-stain and it can be seen from dried droplets of spilled coffee. This coffee-stain effect was first investigated by Deegan et. al. who discovered that these patterns occur when outward radial flows driven by evaporation at the triple contact line dominate over other effects. While the presence of coffee-stain patterns is undesirable in many printing and medical diagnostic processes, it can also be advantageous in the production of low cost transparent conductive films, the deposition of metal vapor, and the manipulation of biological structures. Controlling the interactions between the substrate, liquid, vapor, and particles can lead to control over the size and morphology of evaporative deposition patterns left by aqueous colloidal suspensions. Several methods have been developed to control the evaporation of colloidal suspensions to either suppress or enhance the coffee stain effect. Electrowetting on Dielectric (EWOD) is one promising method that has been used to control colloidal depositions by applying either an AC or DC electric field. EWOD actuation has the potential to dynamically control colloidal deposition left by desiccated droplets to either suppress or enhance the coffee stain effect. It may also allow for independent control of the fluidic interface and deposition of particles via electrowetting and electrokinetic forces

  6. Influence of an Additive-Free Particle Spreading Method on Interactions between Charged Colloidal Particles at an Oil/Water Interface.

    PubMed

    Gao, Peng; Yi, Zonglin; Xing, Xiaochen; Ngai, To; Jin, Fan

    2016-05-17

    The assembly and manipulation of charged colloidal particles at oil/water interfaces represent active areas of fundamental and applied research. Previously, we have shown that colloidal particles can spontaneously generate unstable residual charges at the particle/oil interface when spreading solvent is used to disperse them at an oil/water interface. These residual charges in turn affect the long-ranged electrostatic repulsive forces and packing of particles at the interface. To further uncover the influence arising from the spreading solvents on interfacial particle interactions, in the present study we utilize pure buoyancy to drive the particles onto an oil/water interface and compare the differences between such a spontaneously adsorbed particle monolayer to the spread monolayer based on solvent spreading techniques. Our results show that the solvent-free method could also lead particles to spread well at the interface, but it does not result in violent sliding of particles along the interface. More importantly, this additive-free spreading method can avoid the formation of unstable residual charges at the particle/oil interface. These findings agree well with our previous hypothesis; namely, those unstable residual charges are triboelectric charges that arise from the violently rubbing of particles on oil at the interface. Therefore, if the spreading solvents could be avoided, then we would be able to get rid of the formation of residual charges at interfaces. This finding will provide insight for precisely controlling the interactions among colloidal particles trapped at fluid/fluid interfaces.

  7. Visualization of the equilibrium position of colloidal particles at fluid-water interfaces by deposition of nanoparticles

    NASA Astrophysics Data System (ADS)

    Sabapathy, Manigandan; Kollabattula, Viswas; Basavaraj, Madivala G.; Mani, Ethayaraja

    2015-08-01

    We present a general yet simple method to measure the contact angle of colloidal particles at fluid-water interfaces. In this method, the particles are spread at the required fluid-water interface as a monolayer. In the water phase a chemical reaction involving reduction of a metal salt such as aurochloric acid is initiated. The metal grows as a thin film or islands of nanoparticles on the particle surface exposed to the water side of the interface. Analyzing the images of particles by high resolution scanning microscopy (HRSEM), we trace the three phase contact line up to which deposition of the metal film occurs. From geometrical relations, the three phase contact angle is then calculated. We report the measurements of the contact angle of silica and polystyrene (PS) particles at different interfaces such as air-water, decane-water and octanol-water. We have also applied this method to measure the contact angle of surfactant treated polystyrene particles at the air-water interface, and we find a non-monotonic change of the contact angle with the concentration of the surfactant. Our results are compared with the well-known gel trapping technique and we find good comparison with previous measurements.We present a general yet simple method to measure the contact angle of colloidal particles at fluid-water interfaces. In this method, the particles are spread at the required fluid-water interface as a monolayer. In the water phase a chemical reaction involving reduction of a metal salt such as aurochloric acid is initiated. The metal grows as a thin film or islands of nanoparticles on the particle surface exposed to the water side of the interface. Analyzing the images of particles by high resolution scanning microscopy (HRSEM), we trace the three phase contact line up to which deposition of the metal film occurs. From geometrical relations, the three phase contact angle is then calculated. We report the measurements of the contact angle of silica and polystyrene (PS

  8. Visualization of the equilibrium position of colloidal particles at fluid-water interfaces by deposition of nanoparticles.

    PubMed

    Sabapathy, Manigandan; Kollabattula, Viswas; Basavaraj, Madivala G; Mani, Ethayaraja

    2015-09-07

    We present a general yet simple method to measure the contact angle of colloidal particles at fluid-water interfaces. In this method, the particles are spread at the required fluid-water interface as a monolayer. In the water phase a chemical reaction involving reduction of a metal salt such as aurochloric acid is initiated. The metal grows as a thin film or islands of nanoparticles on the particle surface exposed to the water side of the interface. Analyzing the images of particles by high resolution scanning microscopy (HRSEM), we trace the three phase contact line up to which deposition of the metal film occurs. From geometrical relations, the three phase contact angle is then calculated. We report the measurements of the contact angle of silica and polystyrene (PS) particles at different interfaces such as air-water, decane-water and octanol-water. We have also applied this method to measure the contact angle of surfactant treated polystyrene particles at the air-water interface, and we find a non-monotonic change of the contact angle with the concentration of the surfactant. Our results are compared with the well-known gel trapping technique and we find good comparison with previous measurements.

  9. Non-equilibrium magnetic colloidal dispersions at liquid-air interfaces: dynamic patterns, magnetic order and self-assembled swimmers.

    SciTech Connect

    Snezhko, A.

    2011-04-20

    Colloidal dispersions of interacting particles subjected to an external periodic forcing often develop nontrivial self-assembled patterns and complex collective behavior. A fundamental issue is how collective ordering in such non-equilibrium systems arises from the dynamics of discrete interacting components. In addition, from a practical viewpoint, by working in regimes far from equilibrium new self-organized structures which are generally not available through equilibrium thermodynamics can be created. In this review spontaneous self-assembly phenomena in magnetic colloidal dispersions suspended at liquid-air interfaces and driven out of equilibrium by an alternating magnetic field are presented. Experiments reveal a new type of nontrivially ordered self-assembled structures emerging in such systems in a certain range of excitation parameters. These dynamic structures emerge as a result of the competition between magnetic and hydrodynamic forces and have complex unconventional magnetic ordering. Nontrivial self-induced hydrodynamic fields accompany each out-of-equilibrium pattern. Spontaneous symmetry breaking of the self-induced surface flows leading to a formation of self-propelled microstructures has been discovered. Some features of the self-localized structures can be understood in the framework of the amplitude equation (Ginzburg-Landau type equation) for parametric waves coupled to the conservation law equation describing the evolution of the magnetic particle density and the Navier-Stokes equation for hydrodynamic flows. To understand the fundamental microscopic mechanisms governing self-assembly processes in magnetic colloidal dispersions at liquid-air interfaces a first-principle model for a non-equilibrium self-assembly is presented. The latter model allows us to capture in detail the entire process of out-of-equilibrium self-assembly in the system and reproduces most of the observed phenomenology.

  10. Dynamic Self-Assembly and Self-Propulsion in Nonequilibrium Magnetic Colloidal Ensembles at a Liquid/Liquid Interface

    NASA Astrophysics Data System (ADS)

    Snezhko, Alexey; Aranson, Igor

    2011-03-01

    Ensembles of interacting particles subject to external periodic energy fluxes often develop nontrivial dynamics. Magnetic colloidal particles suspended over an interface of two immiscible liquids and energized by vertical alternating magnetic fields give rise to novel dynamic self-assembled structures (``asters'') which are not accessible at the liquid/air interfaces. Ferromagnetically ordered nickel spherical particles have been used in our experiments. Novel structures are attributed to the interplay between surface waves, generated at the liquid/liquid interface by the collective response of magnetic microparticles to the alternating magnetic field, and hydrodynamic fields induced in the boundary layers of both liquids forming the interface. Two types of magnetic order is reported. We show that self-assembled aster structures become distorted in the presence of a small in-plane dc magnetic field and develop self-propulsion. The speed of locomotion can be effectively tuned by the amplitude of the dc field. The research was supported by the U.S. DOE, Office of Basic Energy Sciences, Division of Materials Science and Engineering, under the Contract No. DE AC02-06CH11357.

  11. Particle contact angles at fluid interfaces: pushing the boundary beyond hard uniform spherical colloids.

    PubMed

    Zanini, Michele; Isa, Lucio

    2016-08-10

    Micro and nanoparticles at fluid interfaces have been attracting increasing interest in the last few decades as building blocks for materials, as mechanical and structural probes for complex interfaces and as models for two-dimensional systems. The three-phase contact angle enters practically all aspects of the particle behavior at the interface: its thermodynamics (binding energy to the interface), dynamics (motion and drag at the interface) and interactions with the interface (adsorption and wetting). Moreover, many interactions among particles at the interface also strongly depend on the contact angle. These concepts have been extensively discussed for non-deformable, homogeneous and mostly spherical particles, but recent progress in particle synthesis and fabrication has instead moved in the direction of producing more complex micro and nanoscale objects, which can be responsive, deformable, heterogenous and/or anisotropic in shape, surface chemistry and material properties. These new particles have a much greater potential for applications and new science, and the study of their behavior at interfaces has only very recently started. In this paper, we critically review the current state of the art of the experimental methods available to measure the contact angle of micro and nanoparticles at fluid interfaces, indicating their strengths and limitations. We then comment on new particle systems that are currently attracting increasing interest in relation to their adsorption and assembly at fluid interfaces and discuss if and which ones of the current techniques are suited to investigate their properties at interfaces. Based on this discussion, we will finally try to indicate a direction in which new experimental methods should develop in the future to tackle the new challenges posed by the novel types of particles that more and more often are used at interfaces.

  12. Phase diagram, design of monolayer binary colloidal crystals, and their fabrication based on ethanol-assisted self-assembly at the air/water interface.

    PubMed

    Dai, Zhengfei; Li, Yue; Duan, Guotao; Jia, Lichao; Cai, Weiping

    2012-08-28

    Flexible structural design and accurate controlled fabrication with structural tunability according to need for binary or multicomponent colloidal crystals have been expected. However, it is still a challenge. In this work, the phase diagram of monolayer binary colloidal crystals (bCCs) is established on the assumption that both large and small polystyrene (PS) colloidal spheres can stay at the air/water interface, and the range diagram for the size ratio and number ratio of small to large colloidal spheres is presented. From this phase diagram, combining the range diagram, we can design and relatively accurately control fabrication of the bCCs with specific structures (or patterns) according to need, including single or mixed patterns with the given relative content. Further, a simple and facile approach is presented to fabricate large-area (more than 10 cm(2)) monolayer bCCs without any surfactants, using differently sized PS spheres, based on ethanol-assisted self-assembly at the air/water interface. bCCs with different patterns and stoichiometries are thus designed from the established phase diagram and then successfully fabricated based on the volume ratios (V(S/L)) of the small to large PS suspensions using the presented colloidal self-assembling method. Interestingly, these monolayer bCCs can be transferred to any desired substrates using water as the medium. This study allows us to design desired patterns of monolayer bCCs and to more accurately control their structures with the used V(S/L).

  13. Preparation of high-quality colloidal mask for nanosphere lithography by a combination of air/water interface self-assembly and solvent vapor annealing.

    PubMed

    Yu, Jie; Geng, Chong; Zheng, Lu; Ma, Zhaohui; Tan, Tianya; Wang, Xiaoqing; Yan, Qingfeng; Shen, Dezhong

    2012-08-28

    Nanosphere lithography (NSL) has been regarded as an inexpensive, inherently parallel, high-throughput, materials-general approach to the fabrication of nanoparticle arrays. However, the order of the resulting nanoparticle array is essentially dependent on the quality of the colloidal monolayer mask. Furthermore, the lateral feature size of the nanoparticles created using NSL is coupled with the diameter of the colloidal spheres, which makes it inconvenient for studying the size-dependent properties of nanoparticles. In this work, we demonstrate a facile approach to the fabrication of a large-area, transferrable, high-quality latex colloidal mask for nanosphere lithography. The approach is based on a combination of the air/water interface self-assembly method and the solvent-vapor-annealing technique. It enables the fabrication of colloidal masks with a higher crystalline integrity compared to those produced by other strategies. By manipulating the diameter of the colloidal spheres and precisely tuning the solvent-vapor-annealing process, flexible control of the size, shape, and spacing of the interstice in a colloidal mask can be realized, which may facilitate the broad use of NSL in studying the size-, shape-, and period-dependent optical, magnetic, electronic, and catalytic properties of nanomaterials.

  14. Adsorption and diffusion of colloidal Au nanoparticles at a liquid-vapor interface.

    PubMed

    Poddar, Nitun N; Amar, Jacques G

    2014-06-28

    Motivated by recent drop-drying experiments of Au nanoparticle (NP) island self-assembly, we investigate the structure, diffusion, and binding of dodecanethiol-coated Au NPs adsorbed at the toluene-vapor interface using molecular dynamics (MD) simulations as well as analytical calculations. For a 6 nm core diameter NP our results indicate the existence of significant intermixing between the ligands and the solvent. As a result, the NP lies primarily below the interface with only a portion of the ligands sticking out, while the toluene-vapor interface is significantly higher in the region above the NP core than away from the NP. These results are consistent with a competition between the negative free energy of mixing of toluene and the dodecanethiol ligands, which tends to keep the NP below the interface, and the effects of surface tension which keeps the NP near the interface. Consistent with this result, we find that the coefficient for nanoparticle diffusion along the interface is close to the Stokes-Einstein prediction for three-dimensional bulk diffusion. An analysis of the ligand arrangement surrounding the NP also indicates that there is relatively little asymmetry in the ligand-coating. We then consider the effects of van der Waals interactions on the adsorption energy. In particular, we derive an analytical expression for the van der Waals interaction energy between a coated nanoparticle and the surrounding solvent along with a closed-form expression for the van der Waals corrections to the binding energy at the interface due to the long-range core-solvent interaction. Using these results along with the results of our MD simulations, we then estimate the van der Waals corrections to the adsorption energy for dodecanethiol-coated Au nanoparticles at the toluene-vapor interface as well as for decanethiol-coated nanoparticles at the water-vapor interface. In both cases, we find that the long-range core-solvent interaction may significantly reduce the binding

  15. Simultaneous investigation of sedimentation and diffusion of a single colloidal particle near an interface.

    PubMed

    Oetama, Ratna J; Walz, John Y

    2006-04-28

    We describe here a new procedure for the simultaneous investigation of sedimentation and diffusion of a colloidal particle in close proximity to a solid, planar wall. The measurements were made using the optical technique of total internal reflection microscopy, coupled with optical radiation pressure, for dimensionless separation distances (gap width/radius of particle) ranging from 0.01 to 0.05. In this region, the hydrodynamic mobility and diffusion coefficient are substantially reduced below bulk values. The procedure involved measuring the mean and the variance of vertical displacements of a Brownian particle settling under gravity toward the plate. The spatially varying diffusion coefficient was calculated from the displacements at small times (where diffusive motion was dominant). The mobility relationship for motion normal to a flat plate was tested by measuring the average distance of travel versus time as the particle settled under the constant force of gravity. For the simple Newtonian fluid used here (aqueous salt solution), the magnitude of the diffusion coefficient and mobility, plus their dependence on separation distance, showed excellent agreement with predictions. This new technique could be of great value in measuring the mobility and diffusion coefficient for near-contact motion in more complex fluids for which the hydrodynamic correction factors are not known a priori, such as shear-thinning fluids.

  16. A semi-analytical calculation of the electrostatic pair interaction between nonuniformly charged colloidal spheres at an air-water interface.

    PubMed

    Lian, Zengju

    2016-07-07

    We study the electrostatic pair interaction between two nonuniformly like-charged colloidal spheres trapped in an air-water interface. Under the linear Poisson-Boltzmann approximation, a general form of the electrostatic potential for the system is shown in terms of multipole expansions. After combining the translation-rotation transform of the coordinates with the numerical multipoint collection, we give a semi-analytical result of the electrostatic pair interaction between the colloids. The pair interaction changes quantitatively or even qualitatively with different distributions of the surface charges on the particles. Because of the anisotropic distribution of the surface charge and the asymmetric dielectric medium, the dipole moment of the ion cloud associating with the particle orients diagonally to the air-water interface with an angle α. When the angle is large, the colloids interact repulsively, while they attract each other when the angle is small. The attractive colloids may be "Janus-like" charged and be arranged with some specific configurations. Whatever the repulsions or the attractions, they all decay asymptotically ∝1/d(3) (d is the center-center distance of the particles) which is consistent with our general acknowledge. The calculation results also provide an insight of the effect of the ion concentration, particle size, and the total charge of the particle on the pair interaction between the particles.

  17. The influence of the membrane-polymer interface on colloidal membrane dynamics and phase behavior

    NASA Astrophysics Data System (ADS)

    Zakhary, Mark J.

    A primary challenge in the field of self-assembly is to identify simple interactions that produce well-defined, complex, and controllable materials. A large part of this task is to creatively engineer appropriate assembly components with such suitable interactions built-in. Here, we demonstrate that rod-like subunits, experimentally modeled by fd bacteriophage viruses, with simple and predictable hard-core repulsive interactions, exhibit a great wealth of fascinating self-assembly behavior. These rods form two-dimensional liquid crystalline colloidal membranes consisting of monolayers of aligned particles owing purely to entropic considerations. Due to surface tension, rods near the edge of the monolayers twist, resulting in an elastic nematic ring surrounding the fluid-like membrane interior, and it is the rich phenomena rooted in the interplay between the edge and the interior that is the subject of this thesis. The chiral nature of the fd subunits causes a symmetry breaking at the membrane edge, which leads to chiral control of interfacial tension and resultantly a controllable, reversible morphological transition between membranes and one-dimensional twisted ribbons. Using optical microscopic and optical tweezer techniques, we show that a nucleation barrier exists in association with the membrane-ribbon transition, and investigate this barrier using fluctuation analysis as well as highly controlled force-extension experiments. The finite bending rigidity of the membrane edge is studied, and we show that long filamentous polymers spontaneously adhere to the edge, introducing the concept of geometrical edge-active agents. By analyzing the suppressed edge fluctuations of filament-bound membranes, it is found that the edge bending rigidity varies by up to an order of magnitude in a predictable and controllable way. Finally, we study the effect of the monolayer edge on the membrane coalescence, and observe two types of stable liquid crystalline defects that form at

  18. Probing Effect of Salinity and pH on Surface Interactions between Air Bubbles and Hydrophobic Solids: Implications on Colloidal Assembly at Air/Water Interface.

    PubMed

    Cui, Xin; Shi, Chen; Zhang, Shuo; Xie, Lei; Liu, Jing; Jiang, Dazhi; Zeng, Hongbo

    2017-04-05

    In this work, bubble probe atomic force microscope (AFM) was employed to quantify the interactions between two air bubbles and between an air bubble and an octadecyltrichlorosilane (OTS)-hydrophobized mica under various aqueous conditions. The key parameters (e.g. surface potentials, decay length of hydrophobic attraction) were obtained by analyzing the measured forces through a theoretical model based on Reynolds lubrication theory and augmented Young-Laplace equation by including effect of disjoining pressure. The bubble-OTS hydrophobic attraction with a decay length of 1.0 nm was found to be independent of solution pH and salinity. These parameters were further used to predict the attachment of OTS-hydrophobized particles onto air/water interface, demonstrating that particle attachment driven by hydrophobic attraction could be facilitated by suppressing electrical double-layer repulsion at low pH or high salinity condition. This facile methodology can be readily extended to quantify interactions of many other colloidal particles with gas/water and oil/water interfaces, with implications on colloidal assembly at different interfaces in many engineering applications.

  19. Floc Growth and Changes in ADV Acoustic Backscatter Signal

    NASA Astrophysics Data System (ADS)

    Rouhnia, M.; Keyvani, A.; Strom, K.

    2013-12-01

    A series of experiments were conducted to examine the effect of mud floc growth on the acoustic back-scatter signal recorded by a Nortek Vector acoustic Doppler velocimeter (ADV). Several studies have shown that calibration equations can be developed to link the backscatter strength with average suspended sediment concentration (SSC) when the sediment particle size distribution remains constant. However, when mud is present, the process of flocculation can alter the suspended particle size distribution. Past studies have shown that it is still unclear as to the degree of dependence of the calibration equation on changes in floc size. Part of the ambiguity lies in the fact that flocs can be porous and rather loosely packed and therefore might not scatter to the same extent as a grain of sand. In addition, direct, detailed measurements of floc size have not accompanied experiments examining the dependence of ADV backscatter and suspended sediment concentration. In this research, a set of laboratory experiments is used to test how floc growth affects the backscatter strength. The laboratory data is examined in light of an analytic model that was developed based on scatter theory to account for changes in both SSC and the floc properties of size and density. For the experiments, a turbulent suspension was created in a tank with a rotating paddle. Fixed concentrations of a mixture of kaolinite and montmorillonite were added to the tank in a step-wise manner. For each step, the flocs were allowed to grow to their equilibrium size before breaking the flocs with high turbulent mixing, adding more sediment, and then returning the mixing rate to a range suitable for the re-growth of flocs. During each floc growth phase, data was simultaneously collected at the same elevation in the tank using a floc camera to capture the changes in floc size, a Nortek Vector ADV for the acoustic backscatter, and a Campbell Scientific OBS 3+ for optical backscatter. Physical samples of the

  20. Cation coordination reactions on nanocrystals: surface/interface, doping control and advanced photocatalysis applications (Conference Presentation)

    NASA Astrophysics Data System (ADS)

    Zhang, Jiatao

    2016-10-01

    Abstract: Including the shape and size effect, the controllable doping, hetero-composite and surface/interface are the prerequisite of colloidal nanocrystals for exploring their optoelectronic properties, such as fluorescence, plasmon-exciton coupling, efficient electron/hole separation, and enhanced photocatalysis applications. By controlling soft acid-base coordination reactions between cation molecular complexes and colloidal nanocrystals, we showed that chemical thermodynamics could drive nanoscale monocrystalline growth of the semiconductor shell on metal nano-substrates and the substitutional heterovalent doping in semiconductor nanocrystals. We have demonstrated evolution of relative position of Au and II-VI semiconductor in Au-Semi from symmetric to asymmetric configuration, different phosphines initiated morphology engineering, oriented attachment of quantum dots into micrometer nanosheets with synergistic control of surface/interface and doing, which can further lead to fine tuning of plasmon-exciton coupling. Therefore, different hydrogen photocatalytic performance, Plasmon enhanced photocatalysis properties have been achieved further which lead to the fine tuning of plasmon-exciton coupling. Substitutional heterovalent doping here enables the tailoring of optical, electronic properties and photocatalysis applications of semiconductor nanocrystals because of electronic impurities (p-, n-type doping) control. References: (1) J. Gui, J. Zhang*, et al. Angew. Chem. Int. Ed. 2015, 54, 3683. (2) Q. Zhao, J. Zhang*, etc., Adv. Mater. 2014, 26, 1387. (3) J. Liu, Q. Zhao, S. G. Wang*, J. Zhang*, etc., Adv. Mater. 2015, 27-2753-2761. (4) H. Qian, J. Zhang*, etc., NPG Asia Mater. (2015) 7, e152. (5) M. Ji, M. Xu, etc., J. Zhang*, Adv. Mater. 2016, in proof. (6) S. Yu, J. T. Zhang, Y. Tang, M. Ouyang*, Nano Lett. 2015, 15, 6282-6288. (7) J. Zhang, Y. Tang, K. Lee and M. Ouyang*, Science 2010, 327, 1634. (8) J. Zhang, Y. Tang, K. Lee, M. Ouyang*, Nature 2010, 466

  1. 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)

  2. Comparison of vapor formation of water at the solid/water interface to colloidal solutions using optically excited gold nanostructures.

    PubMed

    Baral, Susil; Green, Andrew J; Livshits, Maksim Y; Govorov, Alexander O; Richardson, Hugh H

    2014-02-25

    The phase transformation properties of liquid water to vapor is characterized by optical excitation of the lithographically fabricated single gold nanowrenches and contrasted to the phase transformation properties of gold nanoparticles located and optically excited in a bulk solution system [two and three dimensions]. The 532 nm continuous wave excitation of a single gold nanowrench results in superheating of the water to the spinodal decomposition temperature of 580 ± 20 K with bubble formation below the spinodal decomposition temperature being a rare event. Between the spinodal decomposition temperature and the boiling point liquid water is trapped into a metastable state because a barrier to vapor nucleation exists that must be overcome before the thermodynamically stable state is realized. The phase transformation for an optically heated single gold nanowrench is different from the phase transformation of optically excited colloidal gold nanoparticles solution where collective heating effects dominates and leads to the boiling of the solution exactly at the boiling point. In the solution case, the optically excited ensemble of nanoparticles collectively raises the ambient temperature of water to the boiling point where liquid is converted into vapor. The striking difference in the boiling properties of the single gold nanowrench and the nanoparticle solution system can be explained in terms of the vapor-nucleation mechanism, the volume of the overheated liquid, and the collective heating effect. The interpretation of the observed regimes of heating and vaporization is consistent with our theoretical modeling. In particular, we explain with our theory why the boiling with the collective heating in a solution requires 3 orders of magnitude less intensity compared to the case of optically driven single nanowrench.

  3. Effects of bulk colloidal stability on adsorption layers of poly(diallyldimethylammonium chloride)/sodium dodecyl sulfate at the air-water interface studied by neutron reflectometry.

    PubMed

    Campbell, Richard A; Yanez Arteta, Marianna; Angus-Smyth, Anna; Nylander, Tommy; Varga, Imre

    2011-12-29

    We show for the oppositely charged system poly(diallyldimethylammonium chloride)/sodium dodecyl sulfate that the cliff edge peak in its surface tension isotherm results from the comprehensive precipitation of bulk complexes into sediment, leaving a supernatant that is virtually transparent and a depleted adsorption layer at the air/water interface. The aggregation and settling processes take about 3 days to reach completion and occur at bulk compositions around charge neutrality of the complexes which lack long-term colloidal stability. We demonstrate excellent quantitative agreement between the measured surface tension values and a peak calculated from the surface excess of surfactant in the precipitation region measured by neutron reflectometry, using the approximation that there is no polymer left in the liquid phase. The nonequilibrium nature of the system is emphasized by the production of very different interfacial properties from equivalent aged samples that are handled differently. We go on to outline our perspective on the "true equilibrium" state of this intriguing system and conclude with a comment on its practical relevance given that the interfacial properties can be so readily influenced by the handling of kinetically trapped bulk aggregates.

  4. Interface control of electronic and optical properties in IV-VI and II-VI core/shell colloidal quantum dots: a review.

    PubMed

    Jang, Youngjin; Shapiro, Arthur; Isarov, Maya; Rubin-Brusilovski, Anna; Safran, Aron; Budniak, Adam K; Horani, Faris; Dehnel, Joanna; Sashchiuk, Aldona; Lifshitz, Efrat

    2017-01-17

    Semiconductor colloidal quantum dots (CQDs) have attracted vast scientific and technological interest throughout the past three decades, due to the unique tuneability of their optoelectronic properties by variation of size and composition. However, the nanoscale size brings about a large surface-to-bulk volume ratio, where exterior surfaces have a pronounced influence on the chemical stability and on the physical properties of the semiconductor. Therefore, numerous approaches have been developed to gain efficient surface passivation, including a coverage by organic or inorganic molecular surfactants as well as the formation of core/shell heterostructures (a semiconductor core epitaxially covered by another semiconductor shell). This review focuses on special designs of core/shell heterostructures from the IV-VI and II-VI semiconductor compounds, and on synthetic approaches and characterization of the optical properties. Experimental observations revealed the formation of core/shell structures with type-I or quasi-type-II band alignment between the core and shell constituents. Theoretical calculations of the electronic band structures, which were also confirmed by experimental work, exposed surplus electronic tuning (beyond the radial diameter) with adaptation of the composition and control of the interface properties. The studies also considered strain effects that are created between two different semiconductors. It was disclosed experimentally and theoretically that the strain can be released via the formation of alloys at the core-shell interface. Overall, the core/shell and core/alloyed-shell heterostructures showed enhancement in luminescence quantum efficiency with respect to that of pure cores, extended lifetime, uniformity in size and in many cases good chemical sustainability under ambient conditions.

  5. Research Gaps and Technology Needs in Development of PHM for Passive AdvSMR Components

    SciTech Connect

    Meyer, Ryan M.; Ramuhalli, Pradeep; Coble, Jamie B.; Hirt, Evelyn H.; Mitchell, Mark R.; Wootan, David W.; Berglin, Eric J.; Bond, Leonard J.; Henager, Charles H.

    2014-01-01

    Advanced small modular reactors (AdvSMRs), which are based on modularization of advanced reactor concepts, may provide a longer-term alternative to traditional light-water reactors and near term small modular reactors (SMRs), which are based on integral pressurized water reactor (iPWR) concepts. SMRs are challenged economically due to losses in economy of scale, thus, there is increased motivation to reduce the controllable operations and maintenance (O&M) costs through automation technologies including prognostics health management (PHM) systems. In this regard, PHM systems have the potential to play a vital role in supporting the deployment of AdvSMRs and face several unique challenges with respect to implementation for passive AdvSMR components. This paper presents a summary of a research gaps and technical needs assessment performed for implementation of PHM for passive AdvSMR components. state-of-the-art in PHM.

  6. Research gaps and technology needs in development of PHM for passive AdvSMR components

    SciTech Connect

    Meyer, Ryan M.; Ramuhalli, Pradeep; Hirt, Evelyn H.; Mitchell, Mark R.; Wootan, David W.; Berglin, Eric J.; Henagar, Chuck H. Jr.; Coble, Jamie B.; Bond, Leonard J.

    2014-02-18

    Advanced small modular reactors (AdvSMRs), which are based on modularization of advanced reactor concepts, may provide a longer-term alternative to traditional light-water reactors and near-term small modular reactors (SMRs), which are based on integral pressurized water reactor (iPWR) concepts. SMRs are challenged economically because of losses in economy of scale; thus, there is increased motivation to reduce the controllable operations and maintenance costs through automation technologies including prognostics health management (PHM) systems. In this regard, PHM systems have the potential to play a vital role in supporting the deployment of AdvSMRs and face several unique challenges with respect to implementation for passive AdvSMR components. This paper presents a summary of a research gaps and technical needs assessment performed for implementation of PHM for passive AdvSMR components.

  7. 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

  8. Active colloids

    NASA Astrophysics Data System (ADS)

    Aranson, Igor S.

    2013-01-01

    A colloidal suspension is a heterogeneous fluid containing solid microscopic particles. Colloids play an important role in our everyday life, from food and pharmaceutical industries to medicine and nanotechnology. It is useful to distinguish two major classes of colloidal suspensions: equilibrium and active, i.e., maintained out of thermodynamic equilibrium by external electric or magnetic fields, light, chemical reactions, or hydrodynamic shear flow. While the properties of equilibrium colloidal suspensions are fairly well understood, active colloids pose a formidable challenge, and the research is in its early exploratory stage. One of the most remarkable properties of active colloids is the possibility of dynamic self-assembly, a natural tendency of simple building blocks to organize into complex functional architectures. Examples range from tunable, self-healing colloidal crystals and membranes to self-assembled microswimmers and robots. Active colloidal suspensions may exhibit material properties not present in their equilibrium counterparts, e.g., reduced viscosity and enhanced self-diffusivity, etc. This study surveys the most recent developments in the physics of active colloids, both in synthetic and living systems, with the aim of elucidation of the fundamental physical mechanisms governing self-assembly and collective behavior.

  9. 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.

  10. Local-Level Prognostics Health Management Systems Framework for Passive AdvSMR Components. Interim Report

    SciTech Connect

    Ramuhalli, Pradeep; Roy, Surajit; Hirt, Evelyn H.; Pardini, Allan F.; Jones, Anthony M.; Deibler, John E.

    2014-09-12

    This report describes research results to date in support of the integration and demonstration of diagnostics technologies for prototypical AdvSMR passive components (to establish condition indices for monitoring) with model-based prognostics methods. The focus of the PHM methodology and algorithm development in this study is at the localized scale. Multiple localized measurements of material condition (using advanced nondestructive measurement methods), along with available measurements of the stressor environment, enhance the performance of localized diagnostics and prognostics of passive AdvSMR components and systems.

  11. 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.

  12. 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.

  13. 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.

  14. 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

  15. Hexadecapolar Colloids

    DOE PAGES

    Senyuk, Bohdan; Puls, Owen; Tovkach, Oleh M.; ...

    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

  16. Hexadecapolar Colloids

    SciTech Connect

    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. 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 report the ensuing bonding inaccessible to elastic dipoles, quadrupoles and other nematic colloids studied previously.

  17. 76 FR 255 - Amendments To Form ADV; Extension of Compliance Date

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-04

    ... Commission is extending the compliance date generally for four months to provide certain investment advisers... of Investment Adviser Regulation, Division of Investment Management, U.S. Securities and Exchange... Commission adopted amendments to Part 2 of Form ADV , and related rules under the Investment Advisers Act...

  18. Parameter identifiability in application of soft particle electrokinetic theory to determine polymer and polyelectrolyte coating thicknesses on colloids.

    PubMed

    Louie, Stacey M; Phenrat, Tanapon; Small, Mitchell J; Tilton, Robert D; Lowry, Gregory V

    2012-07-17

    Soft particle electrokinetic models have been used to determine adsorbed nonionic polymer and polyelectrolyte layer properties on nanoparticles or colloids by fitting electrophoretic mobility data. Ohshima first established the formalism for these models and provided analytical approximations ( Ohshima, H. Adv. Colloid Interface Sci.1995, 62, 189 ). More recently, exact numerical solutions have been developed, which account for polarization and relaxation effects and require fewer assumptions on the particle and soft layer properties. This paper characterizes statistical uncertainty in the polyelectrolyte layer charge density, layer thickness, and permeability (Brinkman screening length) obtained from fitting data to either the analytical or numerical electrokinetic models. Various combinations of particle core and polymer layer properties are investigated to determine the range of systems for which this analysis can provide a solution with reasonably small uncertainty bounds, particularly for layer thickness. Identifiability of layer thickness in the analytical model ranges from poor confidence for cases with thick, highly charged coatings, to good confidence for cases with thin, low-charged coatings. Identifiability is similar for the numerical model, except that sensitivity is improved at very high charge and permeability, where polarization and relaxation effects are significant. For some poorly identifiable cases, parameter reduction can reduce collinearity to improve identifiability. Analysis of experimental data yielded results consistent with expectations from the simulated theoretical cases. Identifiability of layer charge density and permeability is also evaluated. Guidelines are suggested for evaluation of statistical confidence in polymer and polyelectrolyte layer parameters determined by application of the soft particle electrokinetic theory.

  19. Colloid transport and retention in unsaturated porous media: effect of colloid input concentration.

    PubMed

    Zhang, Wei; Morales, Verónica L; Cakmak, M Ekrem; Salvucci, Anthony E; Geohring, Larry D; Hay, Anthony G; Parlange, Jean-Yves; Steenhuis, Tammo S

    2010-07-01

    Colloids play an important role in facilitating transport of adsorbed contaminants in soils. Recent studies showed that under saturated conditions colloid retention was a function of its concentration. It is unknown if this is the case under unsaturated conditions. In this study, the effect of colloid concentration on colloid retention was investigated in unsaturated columns by increasing concentrations of colloid influents with varying ionic strength. Colloid retention was observed in situ by bright field microscopy and quantified by measuring colloid breakthrough curves. In our unsaturated experiments, greater input concentrations resulted in increased colloid retention at ionic strength above 0.1 mM, but not in deionized water (i.e., 0 mM ionic strength). Bright field microscope images showed that colloid retention mainly occurred at the solid-water interface and wedge-shaped air-water-solid interfaces, whereas the retention at the grain-grain contacts was minor. Some colloids at the air-water-solid interfaces were rotating and oscillating and thus trapped. Computational hydrodynamic simulation confirmed that the wedge-shaped air-water-solid interface could form a "hydrodynamic trap" by retaining colloids in its low velocity vortices. Direct visualization also revealed that colloids once retained acted as new retention sites for other suspended colloids at ionic strength greater than 0.1 mM and thereby could explain the greater retention with increased input concentrations. Derjaguin-Landau-Verwey-Overbeek (DLVO) energy calculations support this concept. Finally, the results of unsaturated experiments were in agreement with limited saturated experiments under otherwise the same conditions.

  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. Stable colloids in molten inorganic salts

    NASA Astrophysics Data System (ADS)

    Zhang, Hao; Dasbiswas, Kinjal; Ludwig, Nicholas B.; Han, Gang; Lee, Byeongdu; Vaikuntanathan, Suri; Talapin, Dmitri V.

    2017-02-01

    A colloidal solution is a homogeneous dispersion of particles or droplets of one phase (solute) in a second, typically liquid, phase (solvent). Colloids are ubiquitous in biological, chemical and technological processes, homogenizing highly dissimilar constituents. To stabilize a colloidal system against coalescence and aggregation, the surface of each solute particle is engineered to impose repulsive forces strong enough to overpower van der Waals attraction and keep the particles separated from each other. Electrostatic stabilization of charged solutes works well in solvents with high dielectric constants, such as water (dielectric constant of 80). In contrast, colloidal stabilization in solvents with low polarity, such as hexane (dielectric constant of about 2), can be achieved by decorating the surface of each particle of the solute with molecules (surfactants) containing flexible, brush-like chains. Here we report a class of colloidal systems in which solute particles (including metals, semiconductors and magnetic materials) form stable colloids in various molten inorganic salts. The stability of such colloids cannot be explained by traditional electrostatic and steric mechanisms. Screening of many solute–solvent combinations shows that colloidal stability can be traced to the strength of chemical bonding at the solute–solvent interface. Theoretical analysis and molecular dynamics modelling suggest that a layer of surface-bound solvent ions produces long-ranged charge-density oscillations in the molten salt around solute particles, preventing their aggregation. Colloids composed of inorganic particles in inorganic melts offer opportunities for introducing colloidal techniques to solid-state science and engineering applications.

  2. 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

  3. 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,...

  4. SACR ADVance 3-D Cartesian Cloud Cover (SACR-ADV-3D3C) product

    DOE Data Explorer

    Meng Wang, Tami Toto, Eugene Clothiaux, Katia Lamer, Mariko Oue

    2017-03-08

    SACR-ADV-3D3C remaps the outputs of SACRCORR for cross-wind range-height indicator (CW-RHI) scans to a Cartesian grid and reports reflectivity CFAD and best estimate domain averaged cloud fraction. The final output is a single NetCDF file containing all aforementioned corrected radar moments remapped on a 3-D Cartesian grid, the SACR reflectivity CFAD, a profile of best estimate cloud fraction, a profile of maximum observable x-domain size (xmax), a profile time to horizontal distance estimate and a profile of minimum observable reflectivity (dBZmin).

  5. Colloid Thrusters, Physics, Fabrication and Performance

    DTIC Science & Technology

    2005-11-17

    Murray, Paulo Lozano and Manuel Martinez-Sanchez, "Mass Spectrometric Analysis of Colloid Thruster Ion Emission from Selected Propellants", JOURNAL...OF PROPULSION AND POWER Vol. 21, No. 3, May-June 2005. 21. Paulo Lozano and Manuel Martinez-Sanchez, "Ionic liquid ion sources: characterization of...externally wetted emitters", Journal of Colloid and Interface Science 282 (2005) 415-421. 22. Paulo Lozano and Manuel Martinez-Sanchez, "Efficiency

  6. Tumor-targeted gene therapy using Adv-AFP-HRPC/IAA prodrug system suppresses growth of hepatoma xenografted in mice.

    PubMed

    Dai, M; Liu, J; Chen, D-E; Rao, Y; Tang, Z-J; Ho, W-Z; Dong, C-Y

    2012-02-01

    Clinical efficacy of current therapies for hepatocellular carcinoma (HCC) treatment is limited. Indole-3-acetic acid (IAA) is non-toxic for mammalian cells. Oxidative decarboxylation of IAA by horseradish peroxidase (HRP) leads to toxic effects of IAA. The purpose of this study was to investigate the effects of a novel gene-targeted enzyme prodrug therapy with IAA on hepatoma growth in vitro and in vivo mouse hepatoma models. We generated a plasmid using adenovirus to express HRP isoenzyme C (HRPC) with the HCC marker, alpha-fetoprotein (AFP), as the promoter (pAdv-AFP-HRPC). Hepatocellular cells were infected with pAdv-AFP-HRPC and treated with IAA. Cell death was detected using MTT assay. Hepatoma xenografts were developed in mice by injection of mouse hepatoma cells. The size and weight of tumors and organs were evaluated. Cell death in tumors was assessed using hematoxylin and eosin-stained tissue sections. HRPC expression in tissues was detected using Reverse Transcriptase-Polymerase Chain Reaction. IAA stimulated death of hepatocellular cells infected with pAdv-AFP-HRPC, in a dose- and time-dependent manner, but not in control cells. Growth of hepatoma xenografts, including the size and weight, was inhibited in mice treated with pAdv-AFP-HRPC and IAA, compared with that in control group. pAdv-AFP-HRPC/IAA treatment induced cell death in hepatoma xenografts in mice. HRPC gene expressed only in hepatoma, but not in other normal organs of mice. pAdv-AFP-HRPC/IAA treatment did not cause any side effects on normal organs. These findings suggest that pAdv-AFP-HRPC/IAA enzyme/prodrug system may serve as a strategy for HCC therapy.

  7. EVALUATION OF RANGE ESTIMATES FOR TOYOTA FCHV-ADV UNDER OPEN ROAD DRIVING CONDITIONS

    SciTech Connect

    Anton, D.; Wipke, K.; Sprik, S.

    2009-07-10

    The objective of this evaluation was to independently and objectively verify driving ranges of >400 miles announced by Toyota for its new advanced Fuel Cell Hybrid Vehicle (FCHV-adv) utilizing 70 MPa compressed hydrogen. To accomplish this, participants from both Savannah River National Laboratory (SRNL) and the National Renewable Energy Laboratory (NREL) witnessed and participated in a 2-vehicle evaluation with Toyota Motor Engineering & Manufacturing North America, Inc. (TEMA) over a typical open road route for over 11 hours in one day with all relevant data recorded. SRNL and TEMA first entered into discussions of verifying the range of the advanced Toyota Fuel Cell Hybrid Vehicle (FCHV-adv) in August 2008 resulting from reported 400+ mile range by Toyota. After extended negotiations, a CRADA agreement, SRNS CRADA No. CR-04-003, was signed on May 6, 2009. Subsequently, on June 30, 2009 SRNL and NREL participated in an all-day evaluation of the FCHV-adv with TEMA to determine the real-world driving range of this vehicle through on-road driving on an extended round-trip drive between Torrance and San Diego, California. SRNL and NREL observed the vehicles being refueled at Toyota's headquarters the day before the evaluation in Torrance, CA on June 29. At 8:00 AM on June 30, the vehicles departed Torrance north toward downtown Los Angeles, then west to the Pacific Coast Highway, and down to San Diego. After lunch the vehicles retraced their route back to Torrance. The traffic encountered was much heavier than anticipated, causing the vehicles to not return to Torrance until 9 PM. Each vehicle was driven by the same Toyota driver all day, with one SRNL/NREL observer in each vehicle the entire route. Data was logged by Toyota and analyzed by NREL. The maximum range of the FCHV-adv vehicles was calculated to be 431 miles under these driving conditions. This distance was calculated from the actual range of 331.5 miles during over 11 hours driving, plus 99.5 miles of

  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. 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.

  10. 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.

  11. 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)

  12. 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.

  13. Plasma interferon-gamma, interleukin-10 and soluble markers of immune activation in infants with primary adenovirus (ADV) and respiratory syncytial virus (RSV) infection.

    PubMed

    Fernández, J Alonso; Tapia, Lorena; Palomino, M Angélica; Larrañaga, Carmen; Peña, Mónica; Jaramillo, Héctor

    2005-01-01

    Adenovirus (ADV) and respiratory syncytial virus (RSV) are etiological agents of acute respiratory tract infection in infants. Long-term prognosis of ADV infection includes severe lung damage, bronchiectasis and hyperlucent lung, while RSV infection is associated with development of recurrent wheezing and subsequent asthma. These differences may be related to differences in the primary immune responses elicited by these viruses. In this paper, we investigated the type of cytokine responses and the magnitude of immune activation in ADV and RSV infections in infants. We examined plasma concentrations of interferon-gamma (IFN-gamma), interleukin-10 (IL-10), soluble interleukin-2 receptor (sCD25) and soluble tumor necrosis factor receptor II (sTNFR-II) in previously healthy infants during the acute phase of primary ADV infection (n = 21) and RSV infection (n = 68), and in uninfected controls (n = 44). In ADV-infected infants, IFN-gamma plasma levels were significantly higher than those observed in RSV cases and the control group (p < 0.05). RSV cases did not show any differences in IFN-gamma plasma levels compared to the other groups. sCD25 levels were significantly higher in ADV- and RSV-infected infants than in controls (p < 0.0001), and higher in ADV than in RSV cases (p < 0.05). sTNFR-II levels were significantly higher in RSV- and ADV-infected infants than in controls (p < 0.0001, p < 0.05, respectively), and higher in RSV than in ADV infection (p < 0.05). No significant differences were observed in IL-10 plasma concentrations between the three groups. These results indicate that ADV and RSV infections in infants differ significantly with regard to the magnitude of production of interferon-gamma and soluble immune activation markers sCD25 and sTNFR-II. These immunological differences may be involved in the different clinical outcomes associated with these viral infections.

  14. Quantifying colloid retention in partially saturated porous media

    NASA Astrophysics Data System (ADS)

    Zevi, Yuniati; Dathe, Annette; Gao, Bin; Richards, Brian K.; Steenhuis, Tammo S.

    2006-12-01

    The transport of colloid-contaminant complexes and colloid-sized pathogens through soil to groundwater is of concern. Visualization and quantification of pore-scale colloid behavior will enable better description and simulation of retention mechanisms at individual surfaces, in contrast to breakthrough curves which only provide an integrated signal. We tested two procedures for quantifying colloid movement and retention as observed in pore-scale image sequences. After initial testing with static images, three series of images of synthetic microbead suspensions passing through unsaturated sand were examined. The region procedure (implemented in ImageJ) and the Boolean procedure (implemented in KS400) yielded nearly identical results for initial test images and for total colloid-covered areas in three image series. Because of electronic noise resulting in pixel-level brightness fluctuations the Boolean procedure tended to underestimate attached colloid counts and conversely overestimate mobile colloid counts. The region procedure had a smaller overestimation error of attached colloids. Reliable quantification of colloid retention at pore scale can be used to improve current understanding on the transport mechanisms of colloids in unsaturated porous media. For example, attachment counts at individual air/water meniscus/solid interface were well described by Langmuir isotherms.

  15. 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.

  16. 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.

  17. 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

  18. Dynamics of evaporative colloidal patterning

    NASA Astrophysics Data System (ADS)

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

    2014-11-01

    Evaporating suspensions of colloidal particles lead to the formation of a variety of patterns, ranging from rings left behind a coffee drop to periodic bands or uniform solid films deposited on a substrate suspended vertically in a container of the colloidal solution. To characterize the transition between different types of patterns, we develop minimal models of the liquid meniscus deformation due to the evaporation and colloidal deposition. A complementary multiphase model allows us to investigate the detailed dynamics of patterning in a drying solvent. This approach couples the inhomogeneous evaporation at the evolving liquid-air interface to the dynamics inside the suspension, i.e. the liquid flow, local variations of the particle concentration, and the propagation of the deposition front where the solute forms a wet, incompressible porous medium at high concentrations. The results of our theory are in good agreement with direct observations. This research was supported by the Air Force Office of Scientific Research (AFOSR) under Award FA9550-09-1-0669-DOD35CAP and the Kavli Institute for Bionano Science and Technology at Harvard University.

  19. 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.

  20. 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

  1. 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.

  2. 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.

  3. Pituitary Colloid Cyst

    PubMed Central

    Guduk, Mustafa; Sun, Halil Ibrahim; Sav, Murat Aydin; Berkman, Zafer

    2017-01-01

    Abstract Colloid cysts appear most commonly in the third ventricle, their occurrence in the sellar region is uncommon. The authors report a female patient with a pituitary colloid cyst. She was diagnosed incidentally with a sellar lesion by a routine paranasal computed tomography examination performed for planning of a dental implant surgery. Radiologic examinations revealed a pituitary lesion that was removed by transnasal transsphenoidal route. Her pathologic examination revealed that the lesion was a colloid cyst. Although rare, colloid cysts should be considered in the differential diagnosis of pituitary lesions PMID:27792102

  4. 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.

  5. Organized assemblies of colloids formed at the poles of micrometer-sized droplets of liquid crystal.

    PubMed

    Wang, Xiaoguang; Miller, Daniel S; de Pablo, Juan J; Abbott, Nicholas L

    2014-11-28

    We report on the formation of organized assemblies of 1 μm-in-diameter colloids (polystyrene (PS)) at the poles of water-dispersed droplets (diameters 7-20 μm) of nematic liquid crystal (LC). For 4-cyano-4'-pentylbiphenyl droplets decorated with two to five PS colloids, we found 32 distinct arrangements of the colloids to form at the boojums of bipolar droplet configurations. Significantly, all but one of these configurations (a ring comprised of five PS colloids) could be mapped onto a local (non-close packed) hexagonal lattice. To provide insight into the origin of the hexagonal lattice, we investigated planar aqueous-LC interfaces, and found that organized assemblies of PS colloids did not form at these interfaces. Experiments involving the addition of salts revealed that a repulsive interaction of electrostatic origin prevented formation of assemblies at planar interfaces, and that regions of high splay near the poles of the LC droplets generated cohesive interactions between colloids that could overcome the repulsion. Support for this interpretation was obtained from a model that included (i) a long-range attraction between adsorbed colloids and the boojum due to the increasing rate of strain (splay) of LC near the boojum (splay attraction), (ii) an attractive inter-colloid interaction that reflects the quadrupolar symmetry of the strain in the LC around the colloids, and (iii) electrostatic repulsion between colloids. The model predicts that electrostatic repulsion between colloids can lead to a ∼1000kBT energy barrier at planar interfaces of LC films, and that the repulsive interaction can be overcome by splay attraction of the colloids to the boojums of the LC droplets. Overall, the results reported in this paper advance our understanding of the directed assembly of colloids at interfaces of LC droplets.

  6. Manipulating semiconductor colloidal stability through doping.

    PubMed

    Fleharty, Mark E; van Swol, Frank; Petsev, Dimiter N

    2014-10-10

    The interface between a doped semiconductor material and electrolyte solution is of considerable fundamental interest, and is relevant to systems of practical importance. Both adjacent domains contain mobile charges, which respond to potential variations. This is exploited to design electronic and optoelectronic sensors, and other enabling semiconductor colloidal materials. We show that the charge mobility in both phases leads to a new type of interaction between semiconductor colloids suspended in aqueous electrolyte solutions. This interaction is due to the electrostatic response of the semiconductor interior to disturbances in the external field upon the approach of two particles. The electrostatic repulsion between two charged colloids is reduced from the one governed by the charged groups present at the particles surfaces. This type of interaction is unique to semiconductor particles and may have a substantial effect on the suspension dynamics and stability.

  7. 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.

  8. 3-D Distribution of Retained Colloids in Unsaturated Porous Media

    NASA Astrophysics Data System (ADS)

    Morales, V. L.; Perez-Reche, F. J.; Holzner, M.; Kinzelbach, W. K.; Otten, W.

    2013-12-01

    It is well accepted that colloid transport processes in porous media differ substantially between water saturated and unsaturated conditions. Differences are frequently ascribed to colloid immobilization by association with interfaces with the gas, as well as to restrictions of the liquid medium through which colloids are transported. Such factors depend on interfacial conditions provided by the water saturation of the porous medium. Yet, the current understanding of the importance of colloid 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 colloidal silver particles were transported for conditions of varying water content. 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 four main locations where colloids can become retained (interfaces with the liquid-solid, gas-liquid and gas-solid, and the bulk liquid), ii) deposition profiles of colloids along the column classified by the available retention location, iii) morphological characteristics of the deposited colloidal aggregates, and iv) channel widths of 3-dimensional pore-water network representations. The results presented provide, for the first time, a direct statistical evaluation on the significance of colloid retention by attachment to the liquid-solid, gas-liquid, gas-solid interfaces, and by straining in the bulk liquid. Additionally, an effective-pore structure characteristic is proposed to improve predictions of mass removal by straining under various water saturations. A) Unsaturated conditions. B) Saturated conditions. Left: Tomograph slice illustrating with false

  9. Colloid-polymer mixtures under slit confinement.

    PubMed

    Pérez-Ramírez, Allan; Figueroa-Gerstenmaier, Susana; Odriozola, Gerardo

    2017-03-14

    We report a NVT molecular dynamic study of colloid-polymer mixtures under slit confinement. For this purpose, we are employing the Asakura-Oosawa model for studying colloidal particles, polymer coils, and hard walls as the external confining field. The colloid-polymer size ratio, q, is varied in the range 1⩾q⩾0.4 and the confinement distance, H, in 10σc⩾H⩾3σc, σc being the colloidal diameter. Vapor-liquid coexistence properties are assessed, from which phase diagrams are built. The obtained data fulfill the corresponding states law for a constant H when q is varied. The shift of the polymer and colloidal chemical potentials of coexistence follows a linear relationship with (H-σc)(-1) for H≳4σc. The confined vapor-liquid interfaces can be fitted with a semicircular line of curvature (H-σc)(-1), from which the contact angle can be obtained. We observe complete wetting of the confining walls for reservoir polymer concentrations above and close to the critical value, and partial wetting for reservoir polymer concentrations above and far from it.

  10. Colloid-polymer mixtures under slit confinement

    NASA Astrophysics Data System (ADS)

    Pérez-Ramírez, Allan; Figueroa-Gerstenmaier, Susana; Odriozola, Gerardo

    2017-03-01

    We report a NVT molecular dynamic study of colloid-polymer mixtures under slit confinement. For this purpose, we are employing the Asakura-Oosawa model for studying colloidal particles, polymer coils, and hard walls as the external confining field. The colloid-polymer size ratio, q, is varied in the range 1 ⩾q ⩾0.4 and the confinement distance, H, in 10 σc ⩾H ⩾3 σc , σc being the colloidal diameter. Vapor-liquid coexistence properties are assessed, from which phase diagrams are built. The obtained data fulfill the corresponding states law for a constant H when q is varied. The shift of the polymer and colloidal chemical potentials of coexistence follows a linear relationship with (H-σc ) -1 for H ≳4 σc . The confined vapor-liquid interfaces can be fitted with a semicircular line of curvature (H-σc ) -1, from which the contact angle can be obtained. We observe complete wetting of the confining walls for reservoir polymer concentrations above and close to the critical value, and partial wetting for reservoir polymer concentrations above and far from it.

  11. Controlled assembly of jammed colloidal shells on fluid droplets.

    PubMed

    Subramaniam, Anand Bala; Abkarian, Manouk; Stone, Howard A

    2005-07-01

    Assembly of colloidal particles on fluid interfaces is a promising technique for synthesizing two-dimensional microcrystalline materials useful in fields as diverse as biomedicine, materials science, mineral flotation and food processing. Current approaches rely on bulk emulsification methods, require further chemical and thermal treatments, and are restrictive with respect to the materials used. The development of methods that exploit the great potential of interfacial assembly for producing tailored materials have been hampered by the lack of understanding of the assembly process. Here we report a microfluidic method that allows direct visualization and understanding of the dynamics of colloidal crystal growth on curved interfaces. The crystals are periodically ejected to form stable jammed shells, which we refer to as colloidal armour. We propose that the energetic barriers to interfacial crystal growth and organization can be overcome by targeted delivery of colloidal particles through hydrodynamic flows. Our method allows an unprecedented degree of control over armour composition, size and stability.

  12. 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.

  13. Model colloid system for interfacial sorption kinetics

    NASA Astrophysics Data System (ADS)

    Salipante, Paul; Hudson, Steven

    2014-11-01

    Adsorption kinetics of nanometer scale molecules, such as proteins at interfaces, is usually determined through measurements of surface coverage. Their small size limits the ability to directly observe individual molecule behavior. To better understand the behavior of nanometer size molecules and the effect on interfacial kinetics, we use micron size colloids with a weak interfacial interaction potential as a model system. Thus, the interaction strength is comparable to many nanoscale systems (less than 10 kBT). The colloid-interface interaction potential is tuned using a combination of depletion, electrostatic, and gravitational forces. The colloids transition between an entropically trapped adsorbed state and a desorbed state through Brownian motion. Observations are made using an LED-based Total Internal Reflection Microscopy (TIRM) setup. The observed adsorption and desorption rates are compared theoretical predictions based on the measured interaction potential and near wall particle diffusivity. This experimental system also allows for the study of more complex dynamics such as nonspherical colloids and collective effects at higher concentrations.

  14. From crystal chemistry to colloid stability

    NASA Astrophysics Data System (ADS)

    Gilbert, B.; Burrows, N.; Penn, R. L.

    2008-12-01

    Aqueous suspensions of ferrihydrite nanoparticles form a colloid with properties that can be understood using classical theories but which additionally exhibit the distinctive phenomenon of nanocluster formation. While use of in situ light and x-ray scattering methods permit the quantitative determination of colloid stability, interparticle interactions, and cluster or aggregate geometry, there are currently few approaches to predict the colloidal behavior of mineral nanoparticles. A longstanding goal of aqueous geochemistry is the rationalization and prediction of the chemical properties of hydrated mineral interfaces from knowledge of interface structure at the molecular scale. Because interfacial acid-base reactions typically lead to the formation of a net electrostatic charge at the surfaces of oxide, hydroxide, and oxyhydroxide mineral surfaces, quantitative descriptions of this behavior have the potential to permit the prediction of long-range interactions between mineral particles. We will evaluate the feasibility of this effort by constructing a model for surface charge formation for ferrihydrite that combines recent insights into the crystal structure of this phase and proposed methods for estimating the pKa of acidic surface groups. We will test the ability of this model to predict the colloidal stability of ferrihydrite suspensions as a function of solution chemistry.

  15. The Neurospora Transcription Factor ADV-1 Transduces Light Signals and Temporal Information to Control Rhythmic Expression of Genes Involved in Cell Fusion

    PubMed Central

    Dekhang, Rigzin; Wu, Cheng; Smith, Kristina M.; Lamb, Teresa M.; Peterson, Matthew; Bredeweg, Erin L.; Ibarra, Oneida; Emerson, Jillian M.; Karunarathna, Nirmala; Lyubetskaya, Anna; Azizi, Elham; Hurley, Jennifer M.; Dunlap, Jay C.; Galagan, James E.; Freitag, Michael; Sachs, Matthew S.; Bell-Pedersen, Deborah

    2016-01-01

    Light and the circadian clock have a profound effect on the biology of organisms through the regulation of large sets of genes. Toward understanding how light and the circadian clock regulate gene expression, we used genome-wide approaches to identify the direct and indirect targets of the light-responsive and clock-controlled transcription factor ADV-1 in Neurospora crassa. A large proportion of ADV-1 targets were found to be light- and/or clock-controlled, and enriched for genes involved in development, metabolism, cell growth, and cell fusion. We show that ADV-1 is necessary for transducing light and/or temporal information to its immediate downstream targets, including controlling rhythms in genes critical to somatic cell fusion. However, while ADV-1 targets are altered in predictable ways in Δadv-1 cells in response to light, this is not always the case for rhythmic target gene expression. These data suggest that a complex regulatory network downstream of ADV-1 functions to generate distinct temporal dynamics of target gene expression relative to the central clock mechanism. PMID:27856696

  16. 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.

  17. 58th Colloid and surface science symposium: program and abstracts

    SciTech Connect

    Not Available

    1984-01-01

    These proceedings contain abstracts of 225 papers presented at the symposium. Papers are grouped under the following categories: dispersions in non-aqueous media; membrane transport and structure; rheology of dispersions and polymer solutions; micellization and microemulsions; fluid/fluid interfaces; spectroscopic characterization of solid/gas and solid/liquid interfaces; structure in concentrated systems; transport phenomena in colloidal systems; polymers at interfaces; and general papers.

  18. Fluctuation forces and wetting layers in colloid-polymer mixtures.

    PubMed

    Hennequin, Y; Aarts, D G A L; Indekeu, J O; Lekkerkerker, H N W; Bonn, D

    2008-05-02

    We present confocal microscopy experiments on the wetting of phase-separated colloid-polymer mixtures. We observe that an unusually thick wetting layer of the colloid-rich phase forms at the walls of the glass container that holds the mixture. Because of the ultralow interfacial tension between the colloid-rich and the polymer-rich phases, the thermally activated roughness of the interfaces becomes very big and measurable. We observe that close to the critical point the roughness of the interface between the wetting layer and the polymer-rich phase decreases with decreasing layer thickness: large excursions of the interface are confined in the wetting layer. The measured relationship between the roughness and the thickness of the wetting layer is in qualitative agreement with the predictions of renormalization group theory for short-range forces and complete wetting.

  19. Brownian diffusion of a partially wetted colloid

    NASA Astrophysics Data System (ADS)

    Boniello, Giuseppe; Blanc, Christophe; Fedorenko, Denys; Medfai, Mayssa; Mbarek, Nadia Ben; in, Martin; Gross, Michel; Stocco, Antonio; Nobili, Maurizio

    2015-09-01

    The dynamics of colloidal particles at interfaces between two fluids plays a central role in microrheology, encapsulation, emulsification, biofilm formation, water remediation and the interface-driven assembly of materials. Common intuition corroborated by hydrodynamic theories suggests that such dynamics is governed by a viscous force lower than that observed in the more viscous fluid. Here, we show experimentally that a particle straddling an air/water interface feels a large viscous drag that is unexpectedly larger than that measured in the bulk. We suggest that such a result arises from thermally activated fluctuations of the interface at the solid/air/liquid triple line and their coupling to the particle drag through the fluctuation-dissipation theorem. Our findings should inform approaches for improved control of the kinetically driven assembly of anisotropic particles with a large triple-line-length/particle-size ratio, and help to understand the formation and structure of such arrested materials.

  20. Magnetic manipulation of self-assembled colloidal asters.

    SciTech Connect

    Snezhko, A.; Aranson, I. S.

    2011-09-01

    Self-assembled materials must actively consume energy and remain out of equilibrium to support structural complexity and functional diversity. Here we show that a magnetic colloidal suspension 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, which exhibit locomotion and shape change. By controlling a small external magnetic field applied parallel to the interface, we show that asters can capture, transport, and position target microparticles. The ability to manipulate colloidal structures is crucial for the further development of self-assembled microrobots

  1. Magnetic manipulation of self-assembled colloidal asters

    NASA Astrophysics Data System (ADS)

    Snezhko, Alexey; Aranson, Igor S.

    2011-09-01

    Self-assembled materials must actively consume energy and remain out of equilibrium to support structural complexity and functional diversity. Here we show that a magnetic colloidal suspension 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, which exhibit locomotion and shape change. By controlling a small external magnetic field applied parallel to the interface, we show that asters can capture, transport, and position target microparticles. The ability to manipulate colloidal structures is crucial for the further development of self-assembled microrobots.

  2. Magnetic manipulation of self-assembled colloidal asters.

    PubMed

    Snezhko, Alexey; Aranson, Igor S

    2011-08-07

    Self-assembled materials must actively consume energy and remain out of equilibrium to support structural complexity and functional diversity. Here we show that a magnetic colloidal suspension 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, which exhibit locomotion and shape change. By controlling a small external magnetic field applied parallel to the interface, we show that asters can capture, transport, and position target microparticles. The ability to manipulate colloidal structures is crucial for the further development of self-assembled microrobots.

  3. Centrifugation-assisted Assembly of Colloidal Silica into Crack-Free and Transferrable Films with Tunable Crystalline Structures

    PubMed Central

    Fan, Wen; Chen, Min; Yang, Shu; Wu, Limin

    2015-01-01

    Self-assembly of colloidal particles into colloidal films has many actual and potential applications. While various strategies have been developed to direct the assembly of colloidal particles, fabrication of crack-free and transferrable colloidal film with controllable crystal structures still remains a major challenge. Here we show a centrifugation-assisted assembly of colloidal silica spheres into free-standing colloidal film by using the liquid/liquid interfaces of three immiscible phases. Through independent control of centrifugal force and interparticle electrostatic repulsion, polycrystalline, single-crystalline and quasi-amorphous structures can be readily obtained. More importantly, by dehydration of silica particles during centrifugation, the spontaneous formation of capillary water bridges between particles enables the binding and pre-shrinkage of the assembled array at the fluid interface. Thus the assembled colloidal films are not only crack-free, but also robust and flexible enough to be easily transferred on various planar and curved substrates. PMID:26159121

  4. Centrifugation-assisted Assembly of Colloidal Silica into Crack-Free and Transferrable Films with Tunable Crystalline Structures.

    PubMed

    Fan, Wen; Chen, Min; Yang, Shu; Wu, Limin

    2015-07-10

    Self-assembly of colloidal particles into colloidal films has many actual and potential applications. While various strategies have been developed to direct the assembly of colloidal particles, fabrication of crack-free and transferrable colloidal film with controllable crystal structures still remains a major challenge. Here we show a centrifugation-assisted assembly of colloidal silica spheres into free-standing colloidal film by using the liquid/liquid interfaces of three immiscible phases. Through independent control of centrifugal force and interparticle electrostatic repulsion, polycrystalline, single-crystalline and quasi-amorphous structures can be readily obtained. More importantly, by dehydration of silica particles during centrifugation, the spontaneous formation of capillary water bridges between particles enables the binding and pre-shrinkage of the assembled array at the fluid interface. Thus the assembled colloidal films are not only crack-free, but also robust and flexible enough to be easily transferred on various planar and curved substrates.

  5. Sampling colloids and colloid-associated contaminants in ground water

    USGS Publications Warehouse

    Backhus, Debera A.; Ryan, Joseph N.; Groher, Daniel M.; MacFarlane, John K.; Gschwend, Philip M.

    1993-01-01

    It has recently been recognized that mobile colloids may affect the transport of contaminants in ground water. To determine the significance of this process, knowledge of both the total mobile load (dissolved + colloid-associated) and the dissolved concentration of a ground-water contaminant must be obtained. Additional information regarding mobile colloid characteristics and concentrations are required to predict accurately the fate and effects of contaminants at sites where significant quantities of colloids are found. To obtain this information, a sampling scheme has been designed and refined to collect mobile colloids while avoiding the inclusion of normally immobile subsurface and well-derived solids. The effectiveness of this sampling protocol was evaluated at a number of contaminated and pristine sites.The sampling results indicated that slow, prolonged pumping of ground water is much more effective at obtaining ground-water samples that represent in situ colloid populations than bailing. Bailed samples from a coal tar-contaminated site contained 10–100 times greater colloid concentrations and up to 750 times greater polycyclic aromatic hydrocarbon concentrations as were detected in slowly pumped samples. The sampling results also indicated that ground-water colloid concentrations should be monitored in the field to determine the adequacy of purging if colloid and colloid-associated contaminants are of interest. To avoid changes in the natural ground-water colloid population through precipitation or coagulation, in situ ground-water chemistry conditions must be preserved during sampling and storage. Samples collected for determination of the total mobile load of colloids and low-solubility contaminants must not be filtered because some mobile colloids are removed by this process. Finally, suggestions that mobile colloids are present in ground water at any particular site should be corroborated with auxiliary data, such as colloid levels in

  6. 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

  7. Software for fitting and simulating fate and transport of dense colloids and biocolloids in one-dimensional porous media: Re-introducing ColloidFit.

    NASA Astrophysics Data System (ADS)

    Katzourakis, Vasileios; Chrysikopoulos, Constantinos

    2016-04-01

    The present work re-introduces ColloidFit, which is an autonomous, modular, multipurpose fitting software for dense colloid and biocolloid transport phenomena in porous media. The initial version of ColloidFit, introduced by Sim and Chrysikopoulos (1995), was substantially improved and combined with a relatively intuitive and easy to use graphical user interface. The re-introduced ColloidFit can simulate the migration of suspended colloid or biocolloid particles in one-dimensional, water saturated, homogeneous porous media with uniform flow, accounting for non-equilibrium attachment onto the solid matrix, as well as gravitational effects. Furthermore, the improved ColloidFit software employs a variety of non-equilibrium, linear and nonlinear models for the simulation of colloid attachment onto a solid matrix under batch experimental conditions. The re-introduced ColloidFit uses the state of the art fitting software "Pest" to estimate unknown model parameter values, together with their 95% confidence intervals. Pest is a model-independent parameter estimation software capable of adjusting model parameters, so that discrepancies between model-generated data and the corresponding experimental measurements are reduced to a user preselected minimum. The fitting process is graphed and displayed in real time. The user is allowed to overview every step of the fitting progress, and if needed to change the initial parameter values. The re-introduced ColloidFit software is expected to make the fitting process of colloid and biocolloid transport data, just a simple task.

  8. Charge-extraction strategies for colloidal quantum dot photovoltaics

    NASA Astrophysics Data System (ADS)

    Lan, Xinzheng; Masala, Silvia; Sargent, Edward H.

    2014-03-01

    The solar-power conversion efficiencies of colloidal quantum dot solar cells have advanced from sub-1% reported in 2005 to a record value of 8.5% in 2013. Much focus has deservedly been placed on densifying, passivating and crosslinking the colloidal quantum dot solid. Here we review progress in improving charge extraction, achieved by engineering the composition and structure of the electrode materials that contact the colloidal quantum dot film. New classes of structured electrodes have been developed and integrated to form bulk heterojunction devices that enhance photocharge extraction. Control over band offsets, doping and interfacial trap state densities have been essential for achieving improved electrical communication with colloidal quantum dot solids. Quantum junction devices that not only tune the optical absorption spectrum, but also provide inherently matched bands across the interface between p- and n-materials, have proven that charge separation can occur efficiently across an all-quantum-tuned rectifying junction.

  9. Armoring confined bubbles in concentrated colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Yu, Yingxian; Khodaparast, Sepideh; Stone, Howard

    2016-11-01

    Encapsulation of a bubble with microparticles is known to significantly improve the stability of the bubble. This phenomenon has recently gained increasing attention due to its application in a variety of technologies such as foam stabilization, drug encapsulation and colloidosomes. Nevertheless, the production of such colloidal armored bubble with controlled size and particle coverage ratio is still a great challenge industrially. We study the coating process of a long air bubble by microparticles in a circular tube filled with a concentrated microparticles colloidal suspension. As the bubble proceeds in the suspension of particles, a monolayer of micro-particles forms on the interface of the bubble, which eventually results in a fully armored bubble. We investigate the phenomenon that triggers and controls the evolution of the particle accumulation on the bubble interface. Moreover, we examine the effects of the mean flow velocity, the size of the colloids and concentration of the suspension on the dynamics of the armored bubble. The results of this study can potentially be applied to production of particle-encapsulated bubbles, surface-cleaning techniques, and gas-assisted injection molding.

  10. A test of the ADV-based Reynolds flux method for in situ estimation of sediment settling velocity in a muddy estuary

    NASA Astrophysics Data System (ADS)

    Cartwright, Grace M.; Friedrichs, Carl T.; Smith, S. Jarrell

    2013-12-01

    Under conditions common in muddy coastal and estuarine environments, acoustic Doppler velocimeters (ADVs) can serve to estimate sediment settling velocity ( w s) by assuming a balance between upward turbulent Reynolds flux and downward gravitational settling. Advantages of this method include simple instrument deployment, lack of flow disturbance, and relative insensitivity to biofouling and water column stratification. Although this method is being used with increasing frequency in coastal and estuarine environments, to date it has received little direct ground truthing. This study compared in situ estimates of w s inferred by a 5-MHz ADV to independent in situ observations from a high-definition video settling column over the course of a flood tide in the bottom boundary layer of the York River estuary, Virginia, USA. The ADV-based measurements were found to agree with those of the settling column when the current speed at about 40 cm above the bed was greater than about 20 cm/s. This corresponded to periods when the estimated magnitude of the settling term in the suspended sediment continuity equation was four or more times larger than the time rate of change of concentration. For ADV observations restricted to these conditions, ADV-based estimates of w s (mean 0.48±0.04 mm/s) were highly consistent with those observed by the settling column (mean 0.45±0.02 mm/s). However, the ADV-based method for estimating w s was sensitive to the prescribed concentration of the non-settling washload, C wash. In an objective operational definition, C wash can be set equal to the lowest suspended solids concentration observed around slack water.

  11. DNA hybridization and ligation for directed colloidal assembly

    NASA Astrophysics Data System (ADS)

    Shyr, Margaret

    membrane to achieve well-ordered colloidal crystals. Well-ordered hexagonally close-packed polystyrene colloid monolayers could be assembled by sedimentation, hybridization, and ligation. Layer-by-layer assembly is also possible on the sedimented colloidal crystals. Since the drying and liquid-air interface effects experienced during vertical deposition are not a factor for sedimented colloidal crystals, we attempted to use templated substrates, created by imprint and holographic lithography, to assemble non-FCC colloidal crystals.

  12. Enhanced adhesion of bioinspired nanopatterned elastomers via colloidal surface assembly

    PubMed Central

    Akerboom, Sabine; Appel, Jeroen; Labonte, David; Federle, Walter; Sprakel, Joris; Kamperman, Marleen

    2015-01-01

    We describe a scalable method to fabricate nanopatterned bioinspired dry adhesives using colloidal lithography. Close-packed monolayers of polystyrene particles were formed at the air/water interface, on which polydimethylsiloxane (PDMS) was applied. The order of the colloidal monolayer and the immersion depth of the particles were tuned by altering the pH and ionic strength of the water. Initially, PDMS completely wetted the air/water interface outside the monolayer, thereby compressing the monolayer as in a Langmuir trough; further application of PDMS subsequently covered the colloidal monolayers. PDMS curing and particle extraction resulted in elastomers patterned with nanodimples. Adhesion and friction of these nanopatterned surfaces with varying dimple depth were studied using a spherical probe as a counter-surface. Compared with smooth surfaces, adhesion of nanopatterned surfaces was enhanced, which is attributed to an energy-dissipating mechanism during pull-off. All nanopatterned surfaces showed a significant decrease in friction compared with smooth surfaces. PMID:25392404

  13. Enhanced adhesion of bioinspired nanopatterned elastomers via colloidal surface assembly.

    PubMed

    Akerboom, Sabine; Appel, Jeroen; Labonte, David; Federle, Walter; Sprakel, Joris; Kamperman, Marleen

    2015-01-06

    We describe a scalable method to fabricate nanopatterned bioinspired dry adhesives using colloidal lithography. Close-packed monolayers of polystyrene particles were formed at the air/water interface, on which polydimethylsiloxane (PDMS) was applied. The order of the colloidal monolayer and the immersion depth of the particles were tuned by altering the pH and ionic strength of the water. Initially, PDMS completely wetted the air/water interface outside the monolayer, thereby compressing the monolayer as in a Langmuir trough; further application of PDMS subsequently covered the colloidal monolayers. PDMS curing and particle extraction resulted in elastomers patterned with nanodimples. Adhesion and friction of these nanopatterned surfaces with varying dimple depth were studied using a spherical probe as a counter-surface. Compared with smooth surfaces, adhesion of nanopatterned surfaces was enhanced, which is attributed to an energy-dissipating mechanism during pull-off. All nanopatterned surfaces showed a significant decrease in friction compared with smooth surfaces.

  14. 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.

  15. Nucleation in food colloids

    NASA Astrophysics Data System (ADS)

    Povey, Malcolm J. W.

    2016-12-01

    Nucleation in food colloids has been studied in detail using ultrasound spectroscopy. Our data show that classical nucleation theory (CNT) remains a sound basis from which to understand nucleation in food colloids and analogous model systems using n-alkanes. Various interpretations and modifications of CNT are discussed with regard to their relevance to food colloids. Much of the evidence presented is based on the ultrasound velocity spectrometry measurements which has many advantages for the study of nucleating systems compared to light scattering and NMR due to its sensitivity at low solid contents and its ability to measure true solid contents in the nucleation and early crystal growth stages. Ultrasound attenuation spectroscopy also responds to critical fluctuations in the induction region. We show, however, that a periodic pressure fluctuation such as a quasi-continuous (as opposed to a pulse comprising only a few pressure cycles) ultrasound field can alter the nucleation process, even at very low acoustic intensity. Thus care must be taken when using ultrasound techniques that the measurements do not alter the studied processes. Quasi-continuous ultrasound fields may enhance or suppress nucleation and the criteria to determine such effects are derived. The conclusions of this paper are relevant to colloidal systems in foods, pharmaceuticals, agro-chemicals, cosmetics, and personal products.

  16. Work Domain Analysis of a Predecessor Sodium-cooled Reactor as Baseline for AdvSMR Operational Concepts

    SciTech Connect

    Ronald Farris; David Gertman; Jacques Hugo

    2014-03-01

    This report presents the results of the Work Domain Analysis for the Experimental Breeder Reactor (EBR-II). This is part of the phase of the research designed to incorporate Cognitive Work Analysis in the development of a framework for the formalization of an Operational Concept (OpsCon) for Advanced Small Modular Reactors (AdvSMRs). For a new AdvSMR design, information obtained through Cognitive Work Analysis, combined with human performance criteria, can and should be used in during the operational phase of a plant to assess the crew performance aspects associated with identified AdvSMR operational concepts. The main objective of this phase was to develop an analytical and descriptive framework that will help systems and human factors engineers to understand the design and operational requirements of the emerging generation of small, advanced, multi-modular reactors. Using EBR-II as a predecessor to emerging sodium-cooled reactor designs required the application of a method suitable to the structured and systematic analysis of the plant to assist in identifying key features of the work associated with it and to clarify the operational and other constraints. The analysis included the identification and description of operating scenarios that were considered characteristic of this type of nuclear power plant. This is an invaluable aspect of Operational Concept development since it typically reveals aspects of future plant configurations that will have an impact on operations. These include, for example, the effect of core design, different coolants, reactor-to-power conversion unit ratios, modular plant layout, modular versus central control rooms, plant siting, and many more. Multi-modular plants in particular are expected to have a significant impact on overall OpsCon in general, and human performance in particular. To support unconventional modes of operation, the modern control room of a multi-module plant would typically require advanced HSIs that would

  17. Effect of fluid-colloid interactions on the mobility of a thermophoretic microswimmer in non-ideal fluids.

    PubMed

    Fedosov, Dmitry A; Sengupta, Ankush; Gompper, Gerhard

    2015-09-07

    Janus colloids propelled by light, e.g., thermophoretic particles, offer promising prospects as artificial microswimmers. However, their swimming behavior and its dependence on fluid properties and fluid-colloid interactions remain poorly understood. Here, we investigate the behavior of a thermophoretic Janus colloid in its own temperature gradient using numerical simulations. The dissipative particle dynamics method with energy conservation is used to investigate the behavior in non-ideal and ideal-gas like fluids for different fluid-colloid interactions, boundary conditions, and temperature-controlling strategies. The fluid-colloid interactions appear to have a strong effect on the colloid behavior, since they directly affect heat exchange between the colloid surface and the fluid. The simulation results show that a reduction of the heat exchange at the fluid-colloid interface leads to an enhancement of colloid's thermophoretic mobility. The colloid behavior is found to be different in non-ideal and ideal fluids, suggesting that fluid compressibility plays a significant role. The flow field around the colloid surface is found to be dominated by a source-dipole, in agreement with the recent theoretical and simulation predictions. Finally, different temperature-control strategies do not appear to have a strong effect on the colloid's swimming velocity.

  18. Effect of fluid-colloid interactions on the mobility of a thermophoretic microswimmer in non-ideal fluids

    NASA Astrophysics Data System (ADS)

    Fedosov, Dmitry A.; Sengupta, Ankush; Gompper, Gerhard

    Janus colloids propelled by light, e.g., thermophoretic particles, offer promising prospects as artificial microswimmers. However, their swimming behavior and its dependence on fluid properties and fluid-colloid interactions remain poorly understood. Here, we investigate the behavior of a thermophoretic Janus colloid in its own temperature gradient using numerical simulations. The dissipative particle dynamics method with energy conservation is used to investigate the behavior in non-ideal and ideal-gas like fluids for different fluid-colloid interactions, boundary conditions, and temperature-controlling strategies. The fluid-colloid interactions appear to have a strong effect on the colloid behavior, since they directly affect heat exchange between the colloid surface and the fluid. The simulation results show that a reduction of the heat exchange at the fluid-colloid interface leads to an enhancement of colloid's thermophoretic mobility. The colloid behavior is found to be different in non-ideal and ideal fluids, suggesting that fluid compressibility plays a significant role. The flow field around the colloid surface is found to be dominated by a source-dipole, in agreement with the recent theoretical and simulation predictions. Finally, different temperature-control strategies do not appear to have a strong effect on the colloid's swimming velocity.

  19. 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.

  20. Non-equilibrium phenomena in disordered colloidal solids

    NASA Astrophysics Data System (ADS)

    Yunker, Peter

    Colloidal particles are a convenient tool for studying a variety of non-equilibrium phenomena. I will discuss experiments that investigate the aging and non-equilibrium growth of disordered solids. In the first set of experiments, colloidal glasses are rapidly formed to study aging in jammed packings. A colloidal fluid, composed of micron-sized temperature-sensitive pNIPAM particles, is rapidly quenched into a colloidal glass. After the glass is formed, collective rearrangements occur as the glass ages. Particles that undergo irreversible rearrangements, which break nearest-neighbor pairings and allow the glass to relax, are identified. These irreversible rearrangements are accompanied by large clusters of fast moving particles; the number of particles involved in these clusters increases as the glass ages, leading to the slowing of dynamics that is characteristic of aging. In the second set of experiments, we study the role particle shape, and thus, interparticle interaction, plays in the formation of disordered solids with different structural and mechanical properties. Aqueous suspensions of colloidal particles with different shapes evaporate on glass slides. Convective flows during evaporation carry particles from drop center to drop edge, where they accumulate. The resulting particle deposits grow heterogeneously from the edge on the air-water interface. Three distinct growth processes were discovered in the evaporating colloidal suspensions by tuning particle shape-dependent capillary interactions and thus varying the microscopic rules of deposition. Mechanical testing of these particulate deposits reveals that the deposit bending rigidity increases as particles become more anisotropic in shape.

  1. Direct visualization of the interfacial position of colloidal particles and their assemblies

    NASA Astrophysics Data System (ADS)

    Vogel, N.; Ally, J.; Bley, K.; Kappl, M.; Landfester, K.; Weiss, C. K.

    2014-05-01

    A method for direct visualization of the position of nanoscale colloidal particles at air-water interfaces is presented. After assembling hard (polystyrene, poly(methyl methacrylate), silica) or soft core-shell gold-hydrogel composite (Au@PNiPAAm) colloids at the air-water interface, butylcyanoacrylate is introduced to the interface via the gas phase. Upon contact with water, an anionic polymerization reaction of the monomer is initiated and a film of poly(butylcyanoacrylate) (PBCA) is generated, entrapping the colloids at their equilibrium position at the interface. We apply this method to investigate the formation of complex, binary assembly structures directly at the interface, to visualize soft, nanoscale hydrogel colloids in the swollen state, and to visualize and quantify the equilibrium position of individual micro- and nanoscale colloids at the air-water interface depending of the amount of charge present on the particle surface. We find that the degree of deprotonation of the carboxyl group shifts the air-water contact angle, which is further confirmed by colloidal probe atomic force microscopy. Remarkably, the contact angles determined for individual colloidal particles feature a significant distribution that greatly exceeds errors attributable to the size distribution of the colloids. This finding underlines the importance of accessing soft matter on an individual particle level.A method for direct visualization of the position of nanoscale colloidal particles at air-water interfaces is presented. After assembling hard (polystyrene, poly(methyl methacrylate), silica) or soft core-shell gold-hydrogel composite (Au@PNiPAAm) colloids at the air-water interface, butylcyanoacrylate is introduced to the interface via the gas phase. Upon contact with water, an anionic polymerization reaction of the monomer is initiated and a film of poly(butylcyanoacrylate) (PBCA) is generated, entrapping the colloids at their equilibrium position at the interface. We apply

  2. 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

  3. 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

  4. Colloidal Material Box: In-situ Observations of Colloidal Self-Assembly and Liquid Crystal Phase Transitions in Microgravity

    NASA Astrophysics Data System (ADS)

    Li, WeiBin; Lan, Ding; Sun, ZhiBin; Geng, BaoMing; Wang, XiaoQing; Tian, WeiQian; Zhai, GuangJie; Wang, YuRen

    2016-05-01

    To study the self-assembly behavior of colloidal spheres in the solid/liquid interface and elucidate the mechanism of liquid crystal phase transition under microgravity, a Colloidal Material Box (CMB) was designed which consists of three modules: (i) colloidal evaporation experimental module, made up of a sample management unit, an injection management unit and an optical observation unit; (ii) liquid crystal phase transition experimental module, including a sample management unit and an optical observation unit; (iii) electronic control module. The following two experimental plans will be performed inside the CMB aboard the SJ-10 satellite in space. (i) Self-assembly of colloidal spheres (with and without Au shell) induced by droplet evaporation, allowing observation of the dynamic process of the colloidal spheres within the droplet and the change of the droplet outer profile during evaporation; (ii) Phase behavior of Mg2Al LDHs suspensions in microgravity. The experimental results will be the first experimental observations of depositing ordered colloidal crystals and their self-assembly behavior under microgravity, and will illustrate the influence of gravity on liquid crystal phase transition.

  5. Development of a model colloidal system for rheology simulation.

    SciTech Connect

    Schunk, Peter Randall; Tallant, David Robert; Piech, Martin; Bell, Nelson Simmons; Frischknecht, Amalie Lucile

    2008-10-01

    The objective of the experimental effort is to provide a model particle system that will enable modeling of the macroscopic rheology from the interfacial and environmental structure of the particles and solvent or melt as functions of applied shear and volume fraction of the solid particles. This chapter describes the choice of the model particle system, methods for synthesis and characterization, and results from characterization of colloidal dispersion, particle film formation, and the shear and oscillatory rheology in the system. Surface characterization of the grafted PDMS interface, dispersion characterization of the colloids, and rheological characterization of the dispersions as a function of volume fraction were conducted.

  6. Fractal nematic colloids

    PubMed Central

    Hashemi, S. M.; Jagodič, U.; Mozaffari, M. R.; Ejtehadi, M. R.; Muševič, I.; Ravnik, M.

    2017-01-01

    Fractals are remarkable examples of self-similarity where a structure or dynamic pattern is repeated over multiple spatial or time scales. However, little is known about how fractal stimuli such as fractal surfaces interact with their local environment if it exhibits order. Here we show geometry-induced formation of fractal defect states in Koch nematic colloids, exhibiting fractal self-similarity better than 90% over three orders of magnitude in the length scales, from micrometers to nanometres. We produce polymer Koch-shaped hollow colloidal prisms of three successive fractal iterations by direct laser writing, and characterize their coupling with the nematic by polarization microscopy and numerical modelling. Explicit generation of topological defect pairs is found, with the number of defects following exponential-law dependence and reaching few 100 already at fractal iteration four. This work demonstrates a route for generation of fractal topological defect states in responsive soft matter. PMID:28117325

  7. Fractal nematic colloids

    NASA Astrophysics Data System (ADS)

    Hashemi, S. M.; Jagodič, U.; Mozaffari, M. R.; Ejtehadi, M. R.; Muševič, I.; Ravnik, M.

    2017-01-01

    Fractals are remarkable examples of self-similarity where a structure or dynamic pattern is repeated over multiple spatial or time scales. However, little is known about how fractal stimuli such as fractal surfaces interact with their local environment if it exhibits order. Here we show geometry-induced formation of fractal defect states in Koch nematic colloids, exhibiting fractal self-similarity better than 90% over three orders of magnitude in the length scales, from micrometers to nanometres. We produce polymer Koch-shaped hollow colloidal prisms of three successive fractal iterations by direct laser writing, and characterize their coupling with the nematic by polarization microscopy and numerical modelling. Explicit generation of topological defect pairs is found, with the number of defects following exponential-law dependence and reaching few 100 already at fractal iteration four. This work demonstrates a route for generation of fractal topological defect states in responsive soft matter.

  8. Fractal nematic colloids.

    PubMed

    Hashemi, S M; Jagodič, U; Mozaffari, M R; Ejtehadi, M R; Muševič, I; Ravnik, M

    2017-01-24

    Fractals are remarkable examples of self-similarity where a structure or dynamic pattern is repeated over multiple spatial or time scales. However, little is known about how fractal stimuli such as fractal surfaces interact with their local environment if it exhibits order. Here we show geometry-induced formation of fractal defect states in Koch nematic colloids, exhibiting fractal self-similarity better than 90% over three orders of magnitude in the length scales, from micrometers to nanometres. We produce polymer Koch-shaped hollow colloidal prisms of three successive fractal iterations by direct laser writing, and characterize their coupling with the nematic by polarization microscopy and numerical modelling. Explicit generation of topological defect pairs is found, with the number of defects following exponential-law dependence and reaching few 100 already at fractal iteration four. This work demonstrates a route for generation of fractal topological defect states in responsive soft matter.

  9. Colloidal interactions between asphaltene surfaces in aqueous solutions.

    PubMed

    Liu, Jianjun; Zhang, Liyan; Xu, Zhenghe; Masliyah, Jacob

    2006-02-14

    Asphaltene at oil/water interfaces plays a dominant role in the recovery of crude oil. In this study, asphaltene monolayer films were deposited on hydrophobic silicon wafers and silica spheres from oil-water interfaces using a Langmuir interfacial trough. The morphology of the deposited asphaltene films was characterized with an atomic force microscope (AFM). The colloidal forces between the prepared asphaltene films in aqueous solutions were measured with AFM to shed light on the stabilization of water or oil droplets coated with asphaltene films. Factors such as solution pH, KCl concentration, calcium addition, and temperature all showed a strong impact on colloidal forces between the prepared asphaltene films. The findings provided a better understanding of asphaltene interfacial films at an oil/water interface in stabilizing bitumen-in-water and water-in-bitumen emulsions.

  10. Colloidal Covalent Organic Frameworks

    PubMed Central

    2017-01-01

    Covalent organic frameworks (COFs) are two- or three-dimensional (2D or 3D) polymer networks with designed topology and chemical functionality, permanent porosity, and high surface areas. These features are potentially useful for a broad range of applications, including catalysis, optoelectronics, and energy storage devices. But current COF syntheses offer poor control over the material’s morphology and final form, generally providing insoluble and unprocessable microcrystalline powder aggregates. COF polymerizations are often performed under conditions in which the monomers are only partially soluble in the reaction solvent, and this heterogeneity has hindered understanding of their polymerization or crystallization processes. Here we report homogeneous polymerization conditions for boronate ester-linked, 2D COFs that inhibit crystallite precipitation, resulting in stable colloidal suspensions of 2D COF nanoparticles. The hexagonal, layered structures of the colloids are confirmed by small-angle and wide-angle X-ray scattering, and kinetic characterization provides insight into the growth process. The colloid size is modulated by solvent conditions, and the technique is demonstrated for four 2D boronate ester-linked COFs. The diameter of individual COF nanoparticles in solution is monitored and quantified during COF growth and stabilization at elevated temperature using in situ variable-temperature liquid cell transmission electron microscopy imaging, a new characterization technique that complements conventional bulk scattering techniques. Solution casting of the colloids yields a free-standing transparent COF film with retained crystallinity and porosity, as well as preferential crystallite orientation. Collectively this structural control provides new opportunities for understanding COF formation and designing morphologies for device applications. PMID:28149954

  11. Flocking ferromagnetic colloids

    PubMed Central

    Kaiser, Andreas; Snezhko, Alexey; Aranson, Igor S.

    2017-01-01

    Assemblages of microscopic colloidal particles exhibit fascinating collective motion when energized by electric or magnetic fields. The behaviors range from coherent vortical motion to phase separation and dynamic self-assembly. Although colloidal systems are relatively simple, understanding their collective response, especially under out-of-equilibrium conditions, remains elusive. We report on the emergence of flocking and global rotation in the system of rolling ferromagnetic microparticles energized by a vertical alternating magnetic field. By combing experiments and discrete particle simulations, we have identified primary physical mechanisms, leading to the emergence of large-scale collective motion: spontaneous symmetry breaking of the clockwise/counterclockwise particle rotation, collisional alignment of particle velocities, and random particle reorientations due to shape imperfections. We have also shown that hydrodynamic interactions between the particles do not have a qualitative effect on the collective dynamics. Our findings shed light on the onset of spatial and temporal coherence in a large class of active systems, both synthetic (colloids, swarms of robots, and biopolymers) and living (suspensions of bacteria, cell colonies, and bird flocks). PMID:28246633

  12. Functional models for colloid retention in porous media at the triple line.

    PubMed

    Dathe, Annette; Zevi, Yuniati; Richards, Brian K; Gao, Bin; Parlange, J-Yves; Steenhuis, Tammo S

    2014-01-01

    Spectral confocal microscope visualizations of microsphere movement in unsaturated porous media showed that attachment at the Air Water Solid (AWS) interface was an important retention mechanism. These visualizations can aid in resolving the functional form of retention rates of colloids at the AWS interface. In this study, soil adsorption isotherm equations were adapted by replacing the chemical concentration in the water as independent variable by the cumulative colloids passing by. In order of increasing number of fitted parameters, the functions tested were the Langmuir adsorption isotherm, the Logistic distribution, and the Weibull distribution. The functions were fitted against colloid concentrations obtained from time series of images acquired with a spectral confocal microscope for three experiments performed where either plain or carboxylated polystyrene latex microspheres were pulsed in a small flow chamber filled with cleaned quartz sand. Both moving and retained colloids were quantified over time. In fitting the models to the data, the agreement improved with increasing number of model parameters. The Weibull distribution gave overall the best fit. The logistic distribution did not fit the initial retention of microspheres well but otherwise the fit was good. The Langmuir isotherm only fitted the longest time series well. The results can be explained that initially when colloids are first introduced the rate of retention is low. Once colloids are at the AWS interface they act as anchor point for other colloids to attach and thereby increasing the retention rate as clusters form. Once the available attachment sites diminish, the retention rate decreases.

  13. Quantification of colloid retention and release by straining and energy minima in variably saturated porous media.

    PubMed

    Sang, Wenjing; Morales, Verónica L; Zhang, Wei; Stoof, Cathelijne R; Gao, Bin; Schatz, Anna Lottie; Zhang, Yalei; Steenhuis, Tammo S

    2013-08-06

    The prediction of colloid transport in unsaturated porous media in the presence of large energy barrier is hampered by scant information of the proportional retention by straining and attractive interactions at surface energy minima. This study aims to fill this gap by performing saturated and unsaturated column experiments in which colloid pulses were added at various ionic strengths (ISs) from 0.1 to 50 mM. Subsequent flushing with deionized water released colloids held at the secondary minimum. Next, destruction of the column freed colloids held by straining. Colloids not recovered at the end of the experiment were quantified as retained at the primary minimum. Results showed that net colloid retention increased with IS and was independent of saturation degree under identical IS and Darcian velocity. Attachment rates were greater in unsaturated columns, despite an over 3-fold increase in pore water velocity relative to saturated columns, because additional retention at the readily available air-associated interfaces (e.g., the air-water-solid [AWS] interfaces) is highly efficient. Complementary visual data showed heavy retention at the AWS interfaces. Retention by secondary minima ranged between 8% and 46% as IS increased, and was greater for saturated conditions. Straining accounted for an average of 57% of the retained colloids with insignificant differences among the treatments. Finally, retention by primary minima ranged between 14% and 35% with increasing IS, and was greater for unsaturated conditions due to capillary pinning.

  14. Increasing entropy for colloidal stabilization

    PubMed Central

    Mo, Songping; Shao, Xuefeng; Chen, Ying; Cheng, Zhengdong

    2016-01-01

    Stability is of paramount importance in colloidal applications. Attraction between colloidal particles is believed to lead to particle aggregation and phase separation; hence, stability improvement can be achieved through either increasing repulsion or reducing attraction by modifying the fluid medium or by using additives. Two traditional mechanisms for colloidal stability are electrostatic stabilization and steric stabilization. However, stability improvement by mixing attractive and unstable particles has rarely been considered. Here, we emphasize the function of mixing entropy in colloidal stabilization. Dispersion stability improvement is demonstrated by mixing suspensions of attractive nanosized titania spheres and platelets. A three-dimensional phase diagram is proposed to illustrate the collaborative effects of particle mixing and particle attraction on colloidal stability. This discovery provides a novel method for enhancing colloidal stability and opens a novel opportunity for engineering applications. PMID:27872473

  15. Equilibrium Shape of Colloidal Crystals.

    PubMed

    Sehgal, Ray M; Maroudas, Dimitrios

    2015-10-27

    Assembling colloidal particles into highly ordered configurations, such as photonic crystals, has significant potential for enabling a broad range of new technologies. Facilitating the nucleation of colloidal crystals and developing successful crystal growth strategies require a fundamental understanding of the equilibrium structure and morphology of small colloidal assemblies. Here, we report the results of a novel computational approach to determine the equilibrium shape of assemblies of colloidal particles that interact via an experimentally validated pair potential. While the well-known Wulff construction can accurately capture the equilibrium shape of large colloidal assemblies, containing O(10(4)) or more particles, determining the equilibrium shape of small colloidal assemblies of O(10) particles requires a generalized Wulff construction technique which we have developed for a proper description of equilibrium structure and morphology of small crystals. We identify and characterize fully several "magic" clusters which are significantly more stable than other similarly sized clusters.

  16. Increasing entropy for colloidal stabilization

    NASA Astrophysics Data System (ADS)

    Mo, Songping; Shao, Xuefeng; Chen, Ying; Cheng, Zhengdong

    2016-11-01

    Stability is of paramount importance in colloidal applications. Attraction between colloidal particles is believed to lead to particle aggregation and phase separation; hence, stability improvement can be achieved through either increasing repulsion or reducing attraction by modifying the fluid medium or by using additives. Two traditional mechanisms for colloidal stability are electrostatic stabilization and steric stabilization. However, stability improvement by mixing attractive and unstable particles has rarely been considered. Here, we emphasize the function of mixing entropy in colloidal stabilization. Dispersion stability improvement is demonstrated by mixing suspensions of attractive nanosized titania spheres and platelets. A three-dimensional phase diagram is proposed to illustrate the collaborative effects of particle mixing and particle attraction on colloidal stability. This discovery provides a novel method for enhancing colloidal stability and opens a novel opportunity for engineering applications.

  17. The Role of Surface Tension in Colloid Retention and Remobilization during Two-phase Flow

    NASA Astrophysics Data System (ADS)

    Zhang, Q.

    2015-12-01

    During unsaturated flow, the accumulation of colloids at fluid-fluid interfaces (AWIs) and fluid-fluid-solid contact lines (AWSs) depend on those areas and surface tension. The area and capillary forces exerting on colloids can be different by adjusting the liquid-liquid surface tension. In the present work, we adjust only surface tension to change the configuration of AWI and AWSs. Experiments were performed in a Polydimethylsiloxane (PDMS) micro-model. Fluorescent carboxylate-modified polystyrene microspheres, with diameter of 300nm were used as model colloids. Water and fluorinert-FC43 were used as the two immiscible liquids. Given the fact that PDMS is a hydrophobic material, fluorinert was the wetting phase and water was the non-wetting phase in this micro-model. Surface tension was changed by adding fluorinert soluble surfactant into fluorinert-FC43. We visualized colloids interacting with the moving fluid-fluid interfaces by confocal microscopy. We also obtained colloid concentration breakthrough curves by measuring the fluorescent intensities in the outlet of the micro-model. The breakthrough curves showed that under steady-state unsaturated flow, less colloid were retained in the system under low surface tension. The visualization results showed that, under low surface tension, the fluid-fluid interfaces are almost flat, thus less area and short contact line available for colloids to attach to. During transient flow, more colloids were remobilized by the moving fluorinert-water interfaces (FWIs) and fluorinert-water-solid contact lines (FWSCs) under high surface tension. Confocal results and measured breakthrough curves confirmed that lowing surface tension decreased capillary force and liquid-liquid area, resulting less retention and remobilization of colloids.

  18. Colloidal Metamaterials at Optical Frequencies

    DTIC Science & Technology

    2014-07-18

    AFRL-OSR-VA-TR-2014-0184 Colloidal Metamaterials at Optical Frequencies Jennifer Dionne LELAND STANFORD JUNIOR UNIV CA Final Report 07/18/2014...Prescribed by ANSI Std. Z39.18 Colloidal Metamaterials at Optical Frequencies Annual Report, June 30, 2014 A. Investigators PI: Jennifer Dionne...team has combined theoretical and experimental methods to produce a colloidally -synthesized metamaterial fluid, or “metafluid,” exhibiting strong

  19. Static and dynamic friction in sliding colloidal monolayers

    PubMed Central

    Vanossi, Andrea; Manini, Nicola; Tosatti, Erio

    2012-01-01

    In a pioneer experiment, Bohlein et al. realized the controlled sliding of two-dimensional colloidal crystals over laser-generated periodic or quasi-periodic potentials. Here we present realistic simulations and arguments that besides reproducing the main experimentally observed features give a first theoretical demonstration of the potential impact of colloid sliding in nanotribology. The free motion of solitons and antisolitons in the sliding of hard incommensurate crystals is contrasted with the soliton–antisoliton pair nucleation at the large static friction threshold Fs when the two lattices are commensurate and pinned. The frictional work directly extracted from particles’ velocities can be analyzed as a function of classic tribological parameters, including speed, spacing, and amplitude of the periodic potential (representing, respectively, the mismatch of the sliding interface and the corrugation, or “load”). These and other features suggestive of further experiments and insights promote colloid sliding to a unique friction study instrument. PMID:23019582

  20. Forced spreading of films and droplets of colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Espin, Leonardo; Kumar, Satish

    2014-11-01

    When a thin film of a colloidal suspension flows over a substrate, uneven distribution of the suspended particles can lead to an uneven coating. Motivated by this phenomenon, we analyse the flow of perfectly wetting films and droplets of colloidal suspensions down an inclined plane. Lubrication theory and the rapid-vertical-diffusion approximation are used to derive a coupled pair of one-dimensional partial differential equations describing the evolution of the interface height and particle concentration. Precursor films are assumed to be present, the colloidal particles are taken to be hard spheres, and particle and liquid dynamics are coupled through a concentration-dependent viscosity and diffusivity. We find that for sufficiently high Péclet numbers, even small initial concentration inhomogeneities produce viscosity gradients that cause the film or droplet front to evolve continuously in time instead of travelling without changing shape as happens in the absence of colloidal particles. Our results suggest that particle concentration gradients can have a dramatic influence on interface evolution in flowing films and droplets, a finding which may be relevant for understanding the onset of patterns that are observed experimentally.

  1. 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.

  2. Colloid retention at the meniscus-wall contact line in an open microchannel.

    PubMed

    Zevi, Yuniati; Gao, Bin; Zhang, Wei; Morales, Verónica L; Cakmak, M Ekrem; Medrano, Evelyn A; Sang, Wenjing; Steenhuis, Tammo S

    2012-02-01

    Colloid retention mechanisms in partially saturated porous media are currently being researched with an array of visualization techniques. These visualization techniques have refined our understanding of colloid movement and retention at the pore scale beyond what can be obtained from breakthrough experiments. One of the remaining questions is what mechanisms are responsible for colloid immobilization at the triple point where air, water, and soil grain meet. The objective of this study was to investigate how colloids are transported to the air-water-solid (AWS) contact line in an open triangular microchannel, and then retained as a function of meniscus contact angle with the wall and solution ionic strength. Colloid flow path, meniscus shape and meniscus-wall contact angle, and colloid retention at the AWS contact line were visualized and quantified with a confocal microscope. Experimental results demonstrated that colloid retention at the AWS contact line was significant when the meniscus-wall contact angle was less than 16°, but was minimal for the meniscus-wall contact angles exceeding 20°. Tracking of individual colloids and computational hydrodynamic simulation both revealed that for small contact angles (e.g., 12.5°), counter flow and flow vortices formed near the AWS contact line, but not for large contact angles (e.g., 28°). This counter flow helped deliver the colloids to the wall surface just below the contact line. In accordance with DLVO and hydrodynamic torque calculations, colloid movement may be stopped when the colloid reached the secondary minimum at the wall near the contact line. However, contradictory to the prediction of the torque analysis, colloid retention at the AWS contact line decreased with increasing ionic strength for contact angles of 10-20°, indicating that the air-water interface was involved through both counter flow and capillary force. We hypothesized that capillary force pushed the colloid through the primary energy

  3. MODFLOW-2000 : the U.S. Geological Survey modular ground-water model--documentation of the Advective-Transport Observation (ADV2) Package

    USGS Publications Warehouse

    Anderman, Evan R.; Hill, Mary Catherine

    2001-01-01

    Observations of the advective component of contaminant transport in steady-state flow fields can provide important information for the calibration of ground-water flow models. This report documents the Advective-Transport Observation (ADV2) Package, version 2, which allows advective-transport observations to be used in the three-dimensional ground-water flow parameter-estimation model MODFLOW-2000. The ADV2 Package is compatible with some of the features in the Layer-Property Flow and Hydrogeologic-Unit Flow Packages, but is not compatible with the Block-Centered Flow or Generalized Finite-Difference Packages. The particle-tracking routine used in the ADV2 Package duplicates the semi-analytical method of MODPATH, as shown in a sample problem. Particles can be tracked in a forward or backward direction, and effects such as retardation can be simulated through manipulation of the effective-porosity value used to calculate velocity. Particles can be discharged at cells that are considered to be weak sinks, in which the sink applied does not capture all the water flowing into the cell, using one of two criteria: (1) if there is any outflow to a boundary condition such as a well or surface-water feature, or (2) if the outflow exceeds a user specified fraction of the cell budget. Although effective porosity could be included as a parameter in the regression, this capability is not included in this package. The weighted sum-of-squares objective function, which is minimized in the Parameter-Estimation Process, was augmented to include the square of the weighted x-, y-, and z-components of the differences between the simulated and observed advective-front locations at defined times, thereby including the direction of travel as well as the overall travel distance in the calibration process. The sensitivities of the particle movement to the parameters needed to minimize the objective function are calculated for any particle location using the exact sensitivity

  4. Experimental study on thermophoresis of colloids in aqueous surfactant solutions

    NASA Astrophysics Data System (ADS)

    Dong, Ruo-Yu; Zhou, Yi; Yang, Chun; Cao, Bing-Yang

    2015-12-01

    Thermophoresis refers to the motion of particles under a temperature gradient and it is one of the particle manipulation techniques. Regarding the thermophoresis of particles in liquid media, however, many open questions still remain, especially the role of the interfacial effect. This work reports on a systematic experimental investigation of surfactant effects, especially the induced interfacial effect, on the thermophoresis of colloids in aqueous solutions via a microfluidic approach. Two kinds of commonly used surfactants, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB), are selected and the results show that from relatively large concentrations, the two surfactants can greatly enhance the thermophilic mobilities. Specifically, it is found that the colloid-water interfaces modified with more polar end groups can potentially lead to a stronger thermophilic tendency. Due to the complex effects of surfactants, further theoretical model development is needed to quantitatively describe the dependence of thermophoresis on the interface characteristics.

  5. Experimental study on thermophoresis of colloids in aqueous surfactant solutions.

    PubMed

    Dong, Ruo-Yu; Zhou, Yi; Yang, Chun; Cao, Bing-Yang

    2015-12-16

    Thermophoresis refers to the motion of particles under a temperature gradient and it is one of the particle manipulation techniques. Regarding the thermophoresis of particles in liquid media, however, many open questions still remain, especially the role of the interfacial effect. This work reports on a systematic experimental investigation of surfactant effects, especially the induced interfacial effect, on the thermophoresis of colloids in aqueous solutions via a microfluidic approach. Two kinds of commonly used surfactants, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB), are selected and the results show that from relatively large concentrations, the two surfactants can greatly enhance the thermophilic mobilities. Specifically, it is found that the colloid-water interfaces modified with more polar end groups can potentially lead to a stronger thermophilic tendency. Due to the complex effects of surfactants, further theoretical model development is needed to quantitatively describe the dependence of thermophoresis on the interface characteristics.

  6. Modeling the co-transport of viruses and colloids in unsaturated porous media.

    PubMed

    Seetha, N; Mohan Kumar, M S; Majid Hassanizadeh, S

    2015-10-01

    A mathematical model is developed to simulate the co-transport of viruses and colloids in unsaturated porous media under steady-state flow conditions. The virus attachment to the mobile and immobile colloids is described using a linear reversible kinetic model. Colloid transport is assumed to be decoupled from virus transport; that is, we assume that colloids are not affected by the presence of attached viruses on their surface. The governing equations are solved numerically using an alternating three-step operator splitting approach. The model is verified by fitting three sets of experimental data published in the literature: (1) Syngouna and Chrysikopoulos (2013) and (2) Walshe et al. (2010), both on the co-transport of viruses and clay colloids under saturated conditions, and (3) Syngouna and Chrysikopoulos (2015) for the co-transport of viruses and clay colloids under unsaturated conditions. We found a good agreement between observed and fitted breakthrough curves (BTCs) under both saturated and unsaturated conditions. Then, the developed model was used to simulate the co-transport of viruses and colloids in porous media under unsaturated conditions, with the aim of understanding the relative importance of various processes on the co-transport of viruses and colloids in unsaturated porous media. The virus retention in porous media in the presence of colloids is greater during unsaturated conditions as compared to the saturated conditions due to: (1) virus attachment to the air-water interface (AWI), and (2) co-deposition of colloids with attached viruses on its surface to the AWI. A sensitivity analysis of the model to various parameters showed that the virus attachment to AWI is the most sensitive parameter affecting the BTCs of both free viruses and total mobile viruses and has a significant effect on all parts of the BTC. The free and the total mobile viruses BTCs are mainly influenced by parameters describing virus attachment to the AWI, virus interaction

  7. Fabrication of planar colloidal clusters with template-assisted interfacial assembly.

    PubMed

    Wirth, Christopher L; De Volder, Michael; Vermant, Jan

    2015-02-10

    The synthesis of nanoparticle clusters, also referred to as colloidal clusters or colloidal molecules, is being studied intensively as a model system for small molecule interactions as well as for the directed self-assembly of advanced materials. This paper describes a technique for the interfacial assembly of planar colloidal clusters using a combination of top-down lithographic surface modification and bottom-up Langmuir-Blodgett deposition. Micrometer sized polystyrene latex particles were deposited onto a chemically modified substrate from a decane-water interface with Langmuir-Blodgett deposition. The surface of the substrate contained hydrophilic domains of various size, spacing, and shape, while the remainder of the substrate was hydrophobic. Particles selectively deposited onto hydrophilic regions from the decane-water interface. The number of deposited particles depended on the size of each patch, thereby demonstrating that tuning cluster size is possible by engineering patch geometry. Following deposition, the clusters were permanently bonded with temperature annealing and then removed from the substrate via sonication. The permanently bonded planar colloidal clusters were stable in an aqueous environment and at a decane-water interface laden with isotropic colloidal particles. The method is a simple and fast way to synthesize colloidal clusters with few limitations on particle chemistry, composition, and shape.

  8. Physics of colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Huang, Jiping

    Colloidal suspensions are complex fluids that consist of mesoscopic particles suspended in a solvent, e.g. water, oil, etc. In this thesis, the objective is to investigate the four aspects of colloidal suspensions: electrorotation, dielectrophoresis, dielectric dispersion spectrum, and nonlinear alternating current (AC) response. The traditional theories failed to fit the recent experimental data, and hence, for the purpose of a better fitting, we aim to develop new theories. In addition, our theories also predicted some new phenomena which are expected to be verified in experiments. Electrorotation has been increasingly employed as a sensitive tool for non-invasive studies of a broad variety of microparticles, ranging from living cells to spores and seeds, as well as synthetic materials. In order to analyze the abundant experimental data, we extend here the existing theory by taking into account crucial elements, such as inhomogeneities, multipolar interactions, nonspherical shapes as well as many-body (local-field) effects. Good agreement is shown between our theoretical results and the experimental data. Dielectrophoresis is typically used for micromanipulation and separation of biological cellular size particles, and it has recently been successfully applied to submicron size particles as well. Specific applications include diverse problems in medicine, colloidal science and nanotechnology. To analyze the recent experimental observations, we present a theory which includes the effects of both charging and multipolar interactions. Our theoretical results are favorably compared with the recent experimental observations. Recent experiments revealed that the dielectric dispersion spectrum of fission yeast cells in a suspension was mainly composed of two sub-dispersions. The low-frequency sub-dispersion depended on the cell length, while the high-frequency one was independent of it. However, the existing theory does not fit the experimental data. Hence, we here put

  9. Light-structured colloidal assemblies

    NASA Astrophysics Data System (ADS)

    Aubret, Antoine; Mena, Youssef; Ramananarivo, Sophie; Sacanna, Stefano; Palacci, Jeremie; Palacci lab Team; Sacanna lab Team

    2016-11-01

    Self-propelled particles (SPP) are a key tool since they are of relative simplicity as compared to biological micro-entities and provide a higher level of control. They can convert an energy source into motion and work, and exhibit surprising non-equilibrium behavior. In our work, we focus on the manipulation of colloids using light. We exploit osmotic and phoretic effects to act on single and ensemble of colloids. The key mechanism relies on the photocatalytic decomposition of hydrogen peroxide using hematite, which triggers the motion of colloids around it when illuminated. We use hematite particles and particles with photocatalytic inclusions (i.e. SPP). We first show that the interactions between hematite and colloidal tracers can be tuned by adjusting the chemical environment. Furthermore, we report a phototaxic behavior (migration in light gradient) of the particles. From this, we explore the effect of spatio-temporal modulation of the light to control the motion of colloids at the single particle level, and to generate self-assembled colloidal structures through time and space. The so-formed structures are maintained by phoretic and hydrodynamic forces resulting from the motion of each particles. Ultimately, a dynamic light modulation may be a route for the creation of active colloidal motion on a collective scale through the synchronization of the individual motions of SPP. This work is supported by NSF CAREER DMR 1554724.

  10. Clathrate colloidal crystals

    NASA Astrophysics Data System (ADS)

    Lin, Haixin; Lee, Sangmin; Sun, Lin; Spellings, Matthew; Engel, Michael; Glotzer, Sharon C.; Mirkin, Chad A.

    2017-03-01

    DNA-programmable assembly has been used to deliberately synthesize hundreds of different colloidal crystals spanning dozens of symmetries, but the complexity of the achieved structures has so far been limited to small unit cells. We assembled DNA-modified triangular bipyramids (~250-nanometer long edge, 177-nanometer short edge) into clathrate architectures. Electron microscopy images revealed that at least three different structures form as large single-domain architectures or as multidomain materials. Ordered assemblies, isostructural to clathrates, were identified with the help of molecular simulations and geometric analysis. These structures are the most sophisticated architectures made via programmable assembly, and their formation can be understood based on the shape of the nanoparticle building blocks and mode of DNA functionalization.

  11. Microfluidic control using colloidal devices.

    PubMed

    Terray, Alex; Oakey, John; Marr, David W M

    2002-06-07

    By manipulating colloidal microspheres within customized channels, we have created micrometer-scale fluid pumps and particulate valves. We describe two positive-displacement designs, a gear and a peristaltic pump, both of which are about the size of a human red blood cell. Two colloidal valve designs are also demonstrated, one actuated and one passive, for the direction of cells or small particles. The use of colloids as both valves and pumps will allow device integration at a density far beyond what is currently achievable by other approaches and may provide a link between fluid manipulation at the macro- and nanoscale.

  12. Microfluidic Control Using Colloidal Devices

    NASA Astrophysics Data System (ADS)

    Terray, Alex; Oakey, John; Marr, David W. M.

    2002-06-01

    By manipulating colloidal microspheres within customized channels, we have created micrometer-scale fluid pumps and particulate valves. We describe two positive-displacement designs, a gear and a peristaltic pump, both of which are about the size of a human red blood cell. Two colloidal valve designs are also demonstrated, one actuated and one passive, for the direction of cells or small particles. The use of colloids as both valves and pumps will allow device integration at a density far beyond what is currently achievable by other approaches and may provide a link between fluid manipulation at the macro- and nanoscale.

  13. Coffee-rings and glasses: Colloids out of equilibrium

    NASA Astrophysics Data System (ADS)

    Yunker, Peter Joseph

    This thesis describes experiments that utilize colloids to explore nonequilibrium phenomena. Specifically, the deposition of particles during evaporation and the glass transition are explored. In the first set of experiments, we found that particle shape has a profound effect on particle deposition. We evaporated drops of colloidal suspensions containing micron-sized particles that range in shape from isotropic spheres to very anisotropic ellipsoids. For sessile drops, i.e., drops sitting on a solid surface, spheres are deposited in a ring-like stain, while ellipsoids are deposited uniformly. We also confined drops between glass plates and allowed them to evaporate. During evaporation, colloidal particles coat the air-water interface, forming colloidal monolayer membranes (CMMs). As particle anisotropy increases, CMM bending rigidity was found to increase. This increase in bending rigidity provides a new mechanism that produces a uniform deposition of ellipsoids and a heterogeneous deposition of spheres. In the second set of experiments, we employed colloidal suspensions to investigate the character of glassy materials. "Anisotropic glasses'' were investigated with ellipsoidal particles confined to two-dimensional chambers at high packing fractions; this system enabled the study of the effects of particle shape on the vibrational properties of colloidal glasses. Low frequency modes in glasses composed of slightly anisotropic particles are found to have predominantly rotational character. Conversely, low frequency modes in glasses of highly anisotropic particles exhibit a mix of rotational and translational character. Aging effects in glasses were explored using suspensions of temperature-sensitive microgel spheres. We devised a method to rapidly quench from liquid to glass states, and then observed the resultant colloidal glasses as they aged. Particle rearrangements in glasses occur collectively, i.e., many particles move in a correlated manner. During aging, we

  14. 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

  15. 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.

  16. 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.

  17. The dielectric response of a colloidal spheroid.

    PubMed

    Chassagne, C; Bedeaux, D

    2008-10-01

    In this article, we present a theory for the dielectric behavior of a colloidal spheroid, based on an improved version of a previously published analytical theory [C. Chassagne, D. Bedeaux, G.J.M. Koper, Physica A 317 (2003) 321-344]. The theory gives the dipolar coefficient of a dielectric spheroid in an electrolyte solution subjected to an oscillating electric field. In the special case of the sphere, this theory is shown to agree rather satisfactorily with the numerical solutions obtained by a code based on DeLacey and White's [E.H.B. DeLacey, L.R. White, J. Chem. Soc. Faraday Trans. 2 77 (1981) 2007] for all zeta potentials, frequencies and kappa a1 where kappa is the inverse of the Debye length and a is the radius of the sphere. Using the form of the analytical solution for a sphere we were able to derive a formula for the dipolar coefficient of a spheroid for all zeta potentials, frequencies and kappa a1. The expression we find is simpler and has a more general validity than the analytical expression proposed by O'Brien and Ward [R.W. O'Brien, D.N. Ward, J. Colloid Interface Sci. 121 (1988) 402] which is valid for kappa a > 1 and zero frequency.

  18. Colloidal nanomaterial-based immunoassay.

    PubMed

    Teste, Bruno; Descroix, Stephanie

    2012-06-01

    Nanomaterials have been widely developed for their use in nanomedicine, especially for immunoassay-based diagnosis. In this review we focus on the use of nanomaterials as a nanoplatform for colloidal immunoassays. While conventional heterogeneous immunoassays suffer from mass transfer limitations and consequently long assay time, colloidal immunosupports allow target capture in the entire volume, thus speeding up reaction kinetics and shortening assay time. Owing to their wide range of chemical and physical properties, nanomaterials are an interesting candidate for immunoassay development. The most popular colloidal nanomaterials for colloidal immunoassays will be discussed, as well as their influence on immune reactions. Recent advances in nanomaterial applications for different formats of immunoassays will be reported, such as nanomaterial-based indirect immunoassays, optical-based agglutination immunoassays, resonance energy transfer-based immunoassays and magnetic relaxation-based immunoassays. Finally, the future of using nanomaterials for homogeneous immunoassays dedicated to clinical diagnosis will be discussed.

  19. Colloids in Flatland: a perspective on 2D phase-separated systems, characterisation methods, and lineactant design.

    PubMed

    Bernardini, C; Stoyanov, S D; Arnaudov, L N; Cohen Stuart, M A

    2013-03-07

    In 1861 Thomas Graham gave birth to a new field of science, today known as colloid science. Nowadays, the notion "colloid" is often used referring to systems consisting of two immiscible phases, one of which is finely dispersed into the other. Research on colloids deals mostly with sols (solids dispersed in a liquid), emulsions (liquids dispersed in liquid), and foams (gas dispersed in a liquid). Because the dispersed particles are small, there is a lot of interface per unit mass. Not surprisingly, therefore, the properties of the interface have often a decisive effect on the behaviour of colloids. Water-air interfaces have a special relevance in this field: many water-insoluble molecules can be spread on water and, given the right spreading conditions and enough available surface area, their spreading proceeds until a monolayer (a one-molecule thick layer) eventually remains. Several 2D phases have been identified for such monolayers, like "gas", "liquid expanded", "liquid condensed", and "solid". The central question of this review is whether these 2D phases can also exist as colloidal systems, and what stabilizes the dispersed state in such systems. We shall present several systems capable of yielding 2D phase separation, from those based on either natural or fluorinated amphiphiles, to polymer-based ones. We shall seek for analogies in 3D and we shall try to clarify if the lines between these 2D objects play a similar role as the interfaces between 3D colloidal systems. In particular, we shall consider the special role of molecules that tend to accumulate at the phase boundaries, that is, at the contact lines, which will therefore be denoted "line-actants" (molecules that adsorb at a 1D interface, separating two 2D colloidal entities), by analogy to the term "surfactant" (which indicates a molecule that adsorbs at a 2D interface separating two 3D colloidal entities).

  20. 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

  1. 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.

  2. 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.

  3. Effect of polymer-polymer interactions on the surface tension of colloid-polymer mixtures

    NASA Astrophysics Data System (ADS)

    Moncho-Jordá, A.; Rotenberg, B.; Louis, A. A.

    2003-12-01

    The density profile and surface tension for the interface of phase-separated colloid-polymer mixtures have been studied in the framework of the square gradient approximation for both ideal and interacting polymers in good solvent. The calculations show that in the presence of polymer-polymer excluded volume interactions the interfaces have lower widths and surface tensions compared to the case of ideal polymers. These results are a direct consequence of the shorter range and smaller depth of the depletion potential between colloidal particles induced by interacting polymers.

  4. A coupled field study of subsurface fracture flow and colloid transport

    NASA Astrophysics Data System (ADS)

    Zhang, Wei; Tang, Xiang-Yu; Weisbrod, Noam; Zhao, Pei; Reid, Brian J.

    2015-05-01

    Field studies of subsurface transport of colloids, which may act as carriers of contaminants, are still rare. This is particularly true for heterogeneous and fractured matrices. To address this knowledge gap, a 30-m long monitoring trench was constructed at the lower end of sloping farmland in central Sichuan, southwest China. During the summer of 2013, high resolution dynamic and temporal fracture flow discharging from the interface between fractured mudrock and impermeable sandstone was obtained at intervals of 5 min (for fast rising stages), 30-60 min (for slow falling stages) or 15 min (at all other times). This discharge was analyzed to elucidate fracture flow and colloid transport in response to rainfall events. Colloid concentrations were observed to increase quickly once rainfall started (∼15-90 min) and reached peak values of up to 188 mg/L. Interestingly, maximum colloid concentration occurred prior to the arrival of flow discharge peak (i.e. maximum colloid concentration was observed before saturation of the soil layer). Rainfall intensity (rather than its duration) was noted to be the main factor controlling colloid response and transport. Dissolved organic carbon concentration and δ18O dynamics in combination with soil water potential were used to apportion water sources of fracture flow at different stages. These approaches suggested the main source of the colloids discharged to be associated with the flushing of colloids from the soil mesopores and macropores. Beyond the scientific interest of colloid mobilization and transport at the field scale, these results have important implications for a region of about 160,000 km2 in southwest China that featured similar hydrogeologic settings as the experimental site. In this agriculture-dominated area, application of pesticides and fertilizers to farmland is prevalent. These results highlight the need to avoid such applications immediately before rainfall events in order to reduce rapid migration to

  5. Transport and retention of colloid particles in partially saturated porous media: effect of surfactant and ionic strength

    NASA Astrophysics Data System (ADS)

    Zevi, Y.; Dathe, A.; Gao, B.; Cakmak, M.; Richards, B. K.; Parlange, J.; Steenhuis, T. S.

    2006-12-01

    The effect of surfactant and ionic strength concentration on colloid transport through saturated or partially saturated media has typically been studied inferentially using breakthrough curves. In this work, we made pore-scale observations in a small flow chamber to count colloids retained on the grain, air and liquid interfaces using a confocal microscope system and public domain image analysis software ImageJ. Stacks of images were analyzed for colloid retention in which the ionic strength and concentration of surfactant (nonionic Surfynol 485) were varied. The number of mobile (free in the water phase) colloids and attached colloids (retained at the surface of sand grains) for each image were quantified. We found that as ionic strength increased, the location where the colloids were retained changed from the air/water meniscus/solid (AWmS) interface to the water/solid (WS) interface. In addition, we observed that increasing the surfactant concentration reduced the retention of colloids due to decreased contact angle and surface tension.

  6. Hierarchical organization of chiral rafts in colloidal membranes

    NASA Astrophysics Data System (ADS)

    Sharma, Prerna; Ward, Andrew; Gibaud, T.; Hagan, Michael F.; Dogic, Zvonimir

    2014-09-01

    Liquid-liquid phase separation is ubiquitous in suspensions of nanoparticles, proteins and colloids. It has an important role in gel formation, protein crystallization and perhaps even as an organizing principle in cellular biology. With a few notable exceptions, liquid-liquid phase separation in bulk proceeds through the continuous coalescence of droplets until the system undergoes complete phase separation. But when colloids, nanoparticles or proteins are confined to interfaces, surfaces or membranes, their interactions differ fundamentally from those mediated by isotropic solvents, and this results in significantly more complex phase behaviour. Here we show that liquid-liquid phase separation in monolayer membranes composed of two dissimilar chiral colloidal rods gives rise to thermodynamically stable rafts that constantly exchange monomeric rods with the background reservoir to maintain a self-limited size. We visualize and manipulate rafts to quantify their assembly kinetics and to show that membrane distortions arising from the rods' chirality lead to long-range repulsive raft-raft interactions. Rafts assemble into cluster crystals at high densities, but they can also form bonds to yield higher-order structures. Taken together, our observations demonstrate a robust membrane-based pathway for the assembly of monodisperse membrane clusters that is complementary to existing methods for colloid assembly in bulk suspensions. They also reveal that chiral inclusions in membranes can acquire long-range repulsive interactions, which might more generally have a role in stabilizing assemblages of finite size.

  7. Investigation of Hydrodynamic and Depletion Interactions in Binary Colloidal Dispersions

    NASA Astrophysics Data System (ADS)

    James, Gregory K.

    Within a colloidal dispersion, the presence of negatively adsorbing material can produce a variety of effects on the dispersion properties and interactions. With increasing concentration, the negatively adsorbing material induces both depletion and structural forces on the dispersion, which can dramatically affect both colloidal stability and near-contact hydrodynamics. This project focused on expanding our understanding of the effects of such negatively adsorbing materials on both equilibrium and dynamic interactions between particles. The effects of charged, hard spheres (silica nanoparticle) on the hydrodynamic drag force a particle experiences as it approaches a flat plate were measured experimentally using colloid probe atomic force microscopy (CP-AFM). Deviation was found between the measured drag force and predictions for the drag force in a simple, Newtonian fluid. The measured drag force was always smaller than the predicted drag force as the particle approached contact with the plate. An effective viscosity, that approached the dispersing fluid viscosity at contact and the bulk viscosity at large separations, was determined for the system. This effective viscosity displayed similar characteristics to those predicted theoretically by Bhattacharya and Blawzdziewicz ( J. Chem. Phys. 2008, 128, 214704.). The effects of both anionic and cationic micelles on the depletion and structural forces in a colloidal dispersion were studied both experimentally (with CP-AFM) and theoretically. The depletion and structural forces between a microparticle and a flat plate were measured and compared with the depletion force predicted by the force-balance model of Walz and Sharma (J. Colloid Interface Sci. 1994, 168, 485-496.). Consistent with previous work, the measured depletion force for both micelles was smaller in magnitude than that predicted by the Walz and Sharma model for hard, charged spheres. It is theorized that rearrangement of the micelle surfaces charges or

  8. Preliminary 3-D site-scale studies of radioactive colloid transortin the unsaturated zone at Yucca Mountain, Nevada

    SciTech Connect

    Moridis, G.J.; Hu, Q.; Wu, Y.-S.; Bodvarsson, G.S.

    2001-09-01

    The U.S: Department of Energy is actively investigating the technical feasibility of permanent disposal of high-level nuclear waste in a repository to be situated in the unsaturated zone at Yucca Mountain, Nevada. In this study we investigate, by means of numerical simulation, the transport of radioactive colloids under ambient conditions from the potential repository horizon to the water table. The site hydrology and the effects of the spatial distribution of hydraulic and transport properties in the Yucca Mountain subsurface are considered. The study of migration and retardation of colloids accounts for the complex processes in the unsaturated zone of Yucca Mountain, and includes advection, diffusion, hydrodynamic dispersion, kinetic colloid filtration, colloid straining, and radioactive decay. The results of the study indicate that the most important factors affecting colloid transport are the subsurface geology and site hydrology, i.e., the presence of faults (they dominate and control transport), fractures (the main migration pathways), and the relative distribution of zeolitic and vitric tuffs. The transport of colloids is strongly influenced by their size (as it affects diffusion into the matrix, straining at hydrogeologic unit interfaces, and transport velocity) and by the parameters of the kinetic-filtration model used for the simulations. Arrival times at the water table decrease with an increasing colloid size because of smaller diffusion, increased straining, and higher transport velocities. The importance of diffusion as a retardation mechanism increases with a decreasing colloid size, but appears to be minimal in large colloids.

  9. Edge pinning and transformation of defect lines induced by faceted colloidal rings in nematic liquid crystals

    NASA Astrophysics Data System (ADS)

    Senyuk, Bohdan; Liu, Qingkun; Yuan, Ye; Smalyukh, Ivan I.

    2016-06-01

    Nematic colloids exhibit a large diversity of topological defects and structures induced by colloidal particles in the orientationally ordered liquid crystal host fluids. These defects and field configurations define elastic interactions and medium-mediated self-assembly, as well as serve as model systems in exploiting the richness of interactions between topologies and geometries of colloidal surfaces, nematic fields, and topological singularities induced by particles in the nematic bulk and at nematic-colloidal interfaces. Here we demonstrate formation of quarter-strength surface-pinned disclinations, as well as a large variety of director field configurations with splitting and reconnections of singular defect lines, prompted by colloidal particles with sharp edges and size large enough to define strong boundary conditions. Using examples of faceted ring-shaped particles of genus g =1 , we explore transformation of defect lines as they migrate between locations in the bulk of the nematic host to edge-pinned locations at the surfaces of particles and vice versa, showing that this behavior is compliant with topological constraints defined by mathematical theorems. We discuss how transformation of bulk and surface defect lines induced by faceted colloids can enrich the diversity of elasticity-mediated colloidal interactions and how these findings may impinge on prospects of their controlled reconfigurable self-assembly in nematic hosts.

  10. Interfacial & colloidal aspects of lipid digestion.

    PubMed

    Wilde, P J; Chu, B S

    2011-06-09

    Amongst the main issues challenging the food manufacturing sector, health and nutrition are becoming increasingly important. Global concerns such as obesity, the ageing population and food security will have to be addressed. Food security is not just about assuring food supply, but is also about optimising nutritional delivery from the food that is available [1]. Therefore one challenge is to optimise the health benefits from the lipids and lipid soluble nutrients. Colloid scientists have an affinity for lipids because they are water insoluble, however this presents a challenge to the digestive system, which has to convert them to structures that are less insoluble so they are available for uptake. Despite this, the human digestive system is remarkably effective at digesting and absorbing most lipids. This is primarily driven through maximising energy intake, as lipids possess the highest calorific value, which was a survival trait to survive times of famine, but is now an underlying cause of obesity in developed countries with high food availability. The critical region here is the lipid-water interface, where the key reactions take place to solubilise lipids and lipid soluble nutrients. Digestive lipases have to adsorb to the oil water interface in order to hydrolyse triacylglycerols into fatty acids and mono glycerides, which accumulate at the interface [2], and inhibit lipase activity. Pancreatic lipase, which is responsible for the majority of lipid hydrolysis, also requires the action of bile salts and colipase to function effectively. Bile salts both aid the adsorption of co-lipase and lipase, and help solubilise the lipolysis products which have accumulated at the interface, into mixed micelles composing bile salts and a range of other lipids, to facilitate transport to the gut mucosal surface prior to uptake and absorption. The process can be affected by the lipid type, as shorter chain, fatty acids are more easily absorbed, whereas the uptake of longer

  11. Quantification of Colloid Retention in Unsaturated Porous Media Using Microscopic Image Analysis Data

    NASA Astrophysics Data System (ADS)

    Dathe, A.; Zevi, Y.; Gao, B.; Richards, B. K.; Steenhuis, T. S.

    2006-05-01

    The movement of contaminants via colloidal transport mechanisms through the vadose zone to groundwater is of growing concern. Normally-immobile contaminants can enter an aquifer via colloid-facilitated transport, and pathogens themselves (e.g. Cryptosporidium parvum) are colloidal in scale. Little is known about the complex pore-scale mechanisms of transport and retention of colloids in soils. Measurements of colloid and microbial transport have been typically limited to the evaluation of breakthrough curves from column experiments (which yield only an integrated signal of all retention processes in the column) or to the visualization in micromodels with limited applicability to realistic conditions. The objective of the work discussed here is to observe and model colloid transport and retention on the pore scale. Flow experiments were run in a horizontal flow chamber containing clean quartz sand as the porous medium. Synthetic fluorescent microspheres were used as easily-detected colloid surrogates. A syringe inlet pump and peristaltic outlet pump controlled the chamber moisture content and flow rate. The chamber was mounted under a Laser Scanning Confocal Microscope (Leica TCS SP2, 10x 0.40 UV objective) which allowed the acquisition of time series images and 3D reconstruction of pore-scale images. Three spectral channels were used to detect: 1) fluorescent microsphere emissions (500 to 540 nm) excited at 488 nm by an argon laser; 2) water phase emissions (555 to 650 nm) due to Rhodamine B stain excited at 543 nm by a green HeNe laser; and 3) reflectance of laser light at the grain surfaces. Three 8-bit images were detected simultaneously for every time step. The system is also capable of obtaining image stacks in the z-direction, which allow the determination of the position of attached colloids relative to the interface between air, water menisci, and solid grains. The 3D z-axis stacks reveal that the colloids are attaching at the air/water meniscus/solid (AWm

  12. Colloids in the vicinity of landfills

    NASA Astrophysics Data System (ADS)

    Baumann, T.; Fruhstorfer, P.; Klein, T.; Niessner, R.

    2003-04-01

    Waste disposals without adequate landfill liner system are a source of contaminants and colloids. In order to assess the effects of the presence of colloids on the transport of heavy metal ions, the colloids at three landfill sites were characterized with regard to their chemical and mineralogical composition, their size distribution, and the concentration of heavy metal ions associated to the colloids. It can be shown that the pattern of the colloids inside and outside of the landfill is different in all examined parameters, e.g. inside of the disposal we find organic colloids and salt particles, whereas the groundwater downstream of the disposal contains mainly iron-colloids and carbonatic particles. Therefore a direct transfer of colloids from the landfill to the aquifer seems unlikely. Changes of the hydrochemical (mainly redox) and hydrodynamic conditions contribute to this behaviour. The association of heavy metal ions to colloids shows an interesting pattern: High concentrations are present in solution and associated to smaller (< 10 nm) and larger (> 1 μm) colloids, whereas the colloids in between show only small concentrations. This finding has some impact on the assessment of colloidal transport processes, since it suggests, that the more mobile colloids do not carry high concentrations of heavy metal ions.

  13. Coalescence, evaporation and particle deposition of consecutively printed colloidal drops

    NASA Astrophysics Data System (ADS)

    Chhasatia, Viral; Yang, Xin; Shah, Jaymeen; Sun, Ying

    2012-11-01

    In applications such as inkjet printing and spray deposition, colloid drops are often used as building blocks for line and pattern printing where their interactions play important roles in determining the deposition morphology and properties. In this study, the particle deposition dynamics of two consecutively printed evaporating colloidal drops is examined using a fluorescence microscope and a synchronized side-view camera. The results show that the relaxation time of the water-air interface of the merged drop is shorter than that of a single drop impacting on a dry surface. It is also found that both morphology and particle distribution uniformity of the deposit change significantly with varying jetting delay and spatial spacing between two drops. As the drop spacing increases while keeping jetting delay constant, the circularity of the coalesced drop reduces. For the regime where the time scale for drop evaporation is comparable with the relaxation time scale for two drops to completely coalesce, the capillary flow induced by the local curvature variation of the air-water interface redistributes particles inside a merged drop, causing suppression of the coffee-ring effect for the case of a high jetting frequency while resulting in a region of particle accumulation in the middle of the merged drop at a low jetting frequency. By tuning the interplay of wetting, evaporation, capillary relaxation, and particle assembly, the deposition morphology of consecutively printed colloidal drops can be controlled.

  14. Exploiting the colloidal nanocrystal library to construct electronic devices

    NASA Astrophysics Data System (ADS)

    Choi, Ji-Hyuk; Wang, Han; Oh, Soong Ju; Paik, Taejong; Sung, Pil; Sung, Jinwoo; Ye, Xingchen; Zhao, Tianshuo; Diroll, Benjamin T.; Murray, Christopher B.; Kagan, Cherie R.

    2016-04-01

    Synthetic methods produce libraries of colloidal nanocrystals with tunable physical properties by tailoring the nanocrystal size, shape, and composition. Here, we exploit colloidal nanocrystal diversity and design the materials, interfaces, and processes to construct all-nanocrystal electronic devices using solution-based processes. Metallic silver and semiconducting cadmium selenide nanocrystals are deposited to form high-conductivity and high-mobility thin-film electrodes and channel layers of field-effect transistors. Insulating aluminum oxide nanocrystals are assembled layer by layer with polyelectrolytes to form high-dielectric constant gate insulator layers for low-voltage device operation. Metallic indium nanocrystals are codispersed with silver nanocrystals to integrate an indium supply in the deposited electrodes that serves to passivate and dope the cadmium selenide nanocrystal channel layer. We fabricate all-nanocrystal field-effect transistors on flexible plastics with electron mobilities of 21.7 square centimeters per volt-second.

  15. A quick and simple route to form soft Janus colloids

    NASA Astrophysics Data System (ADS)

    Sosa, Chris; Priestley, Rodney; Prud'Homme, Robert

    2014-03-01

    Janus colloids, i.e., particles with two chemically distinct compartments or ``faces,'' are of significant scientific interest as they could serve as the enabling material for self-organizing superstructures and functional nanodevices. The internally segregated structures present in Janus particles are not only beneficial for self-assembly applications, but are also attractive from a more fundamental scientific perspective for the insight they can provide on hybrid material interfaces. Here, we present a novel, one-step nano-precipitation process for the formation of soft Janus colloids composed of two compositionally distinct and surface-active polymer domains. In particular, this approach allows for the fabrication of Janus particles from both homopolymers and block co-polymers, generates phase-separated Janus structures on extremely fast timescales, and provides excellent scalability. Supported, in part, by the Department of Energy (DOE) Office of Science Graduate Fellowship Program (DOE SCGF).

  16. Pattern transition and sluggish cracking of colloidal droplet deposition with polymer additives

    NASA Astrophysics Data System (ADS)

    Zhang, YongJian; Liu, ZhengTang; Zang, DuYang; Qian, YiMeng; Lin, KeJun

    2013-09-01

    Drying of colloidal droplets often develops versatile depositions. We study the drying deposition of both colloidal droplets containing silica nanoparticles and the silica colloidal droplets with polyethylene oxide (PEO) additives. We focus on the effect of polymer additives on the deposition formation and the cracking dynamics by using in-situ microscope observation. With PEO additives, a transition from ring-like deposition to uniform deposition is observed, and the cracking dynamics is greatly reduced. The PEO additives enhance the adsorption of particles at the air-water interface, thus forming the network structure at the interface which blocks the outward capillary flow. This contributes to the uniform deposition. Meanwhile, the multi-distribution of the aggregates size enhances the non-homogeneity of the drying film and consequently results in multi-nucleation of cracks. This reduces the stress accumulation that drives the crack propagation and may be responsible for the sluggish cracking dynamics.

  17. Colloid Transport in Unsaturated Porous Media: 3D Visualization Using Synchrotron X-Ray Microtomography

    NASA Astrophysics Data System (ADS)

    Brueck, C. L.; Meisenheimer, D.; Wildenschild, D.

    2015-12-01

    Understanding the mechanisms controlling colloid transport and deposition in the vadose zone is an important step in protecting our water resources. Not only may these particles themselves be undesirable contaminants, but they can also aid in the transport of smaller, molecular-scale contaminants by chemical attachment. In this research, we examined the influence that air-water interfaces (AWI) and air-water-solid contact lines (AWS) have on colloid deposition and mobilization in three-dimensional systems. We used x-ray microtomography to visualize the transport of hydrophobic colloids as they move through a partially saturated glass bead pack. Drainage and imbibition experiments were conducted using syringe pumps to control the flow of a colloid suspension through the porous media at 0.6 mL/hr. The high ionic strength fluid was adjusted to a pH of 9.5 and a concentration of 1.0 mol/L KI. During the drainage and imbibition, the flow was periodically halted and allowed to equilibrate before collecting the microtomography scans. Dopants were used to enhance the contrast between the four phases (water, air, beads, and colloids), including potassium iodide dissolved in the fluid, and an outer layer of silver coating the colloids. We hypothesized that AWIs and AWSs will scour and mobilize a significant percentage of colloids, and therefore reduce the concentration of colloids along the vertical profile of the column. The concentration of potassium iodide, and thus the ionic strength, necessary for adequate image segmentation was also explored in separate experiments so that the influence of ionic strength on colloid deposition and mobilization can be studied.

  18. Coupling of physical and chemical mechanisms of colloid straining in saturated porous media.

    PubMed

    Bradford, Scott A; Torkzaban, Saeed; Walker, Sharon L

    2007-07-01

    Filtration theory does not include the potential influence of pore structure on colloid removal by straining. Conversely, previous research on straining has not considered the possible influence of chemical interactions. Experimental and theoretical studies were therefore undertaken to explore the coupling of physical and chemical mechanisms of colloid straining under unfavorable attachment conditions (pH=10). Negatively charged latex microspheres (1.1 and 3 microm) and quartz sands (360, 240, and 150 microm) were used in packed column studies that encompassed a range in suspension ionic strengths (6-106 mM) and Darcy water velocities (0.1-0.45 cm min(-1)). Derjaguin-Landau-Verwey-Overbeek (DLVO) calculations and torque analysis suggests that attachment of colloids to the solid-water interface was not a significant mechanism of deposition for the selected experimental conditions. Effluent concentration curves and hyperexponential deposition profiles were strongly dependent on the solution chemistry, the system hydrodynamics, and the colloid and collector grain size, with greater deposition occurring for increasing ionic strength, lower flow rates, and larger ratios of the colloid to the median grain diameter. Increasing the solution ionic strength is believed to increase the force and number of colloids in the secondary minimum of the DLVO interaction energy profile. These weakly associated colloids can be funneled to small regions of the pore space formed adjacent to grain-grain junctions. For select systems, the ionic strength of the eluant solution was decreased to 6mM following the recovery of the effluent concentration curve. In this case, only a small portion of the deposited colloids was recovered in the effluent and the majority was still retained in the sand. These observations suggest that the extent of colloid removal by straining is strongly coupled to solution chemistry.

  19. 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.

  20. 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

  1. Electrohydrodynamic simulation of an electrospray in a colloid thruster

    NASA Astrophysics Data System (ADS)

    Jugroot, Manish; Forget, Martin; Malardier-Jugroot, Cecile

    2012-02-01

    A precise understanding of electrosprays is highly interesting as the complexity of micro-technology (such as nano-material processing, spacecraft propulsion and mass-spectrometers) systems increases. A multi-component CFD-based model coupling fluid dynamics, charged species dynamics and electric field is developed. The simulations describe the charged fluid interface with emphasis on the Taylor cone formation and cone-jet transition under the effect of a electric field. The goal is to recapture this transition from a rounded liquid interface into a Taylor cone from an initial uniform distribution, without making assumptions on the behaviour, geometry or charge distribution of the system. The time evolution of the interface highlights the close interaction among space charge, coulombic forces and the surface tension, which appear as governing and competing processes in the transition. The results from the coupled formalism provide valuable insights on the physical phenomena and will be applied to a colloid thruster for small spacecrafts.

  2. Site-specific retention of colloids at rough rock surfaces.

    PubMed

    Darbha, Gopala Krishna; Fischer, Cornelius; Luetzenkirchen, Johannes; Schäfer, Thorsten

    2012-09-04

    The spatial deposition of polystyrene latex colloids (d = 1 μm) at rough mineral and rock surfaces was investigated quantitatively as a function of Eu(III) concentration. Granodiorite samples from Grimsel test site (GTS), Switzerland, were used as collector surfaces for sorption experiments. At a scan area of 300 × 300 μm(2), the surface roughness (rms roughness, Rq) range was 100-2000 nm, including roughness contribution from asperities of several tens of nanometers in height to the sample topography. Although, an increase in both roughness and [Eu(III)] resulted in enhanced colloid deposition on granodiorite surfaces, surface roughness governs colloid deposition mainly at low Eu(III) concentrations (≤5 × 10(-7) M). Highest deposition efficiency on granodiorite has been found at walls of intergranular pores at surface sections with roughness Rq = 500-2000 nm. An about 2 orders of magnitude lower colloid deposition has been observed at granodiorite sections with low surface roughness (Rq < 500 nm), such as large and smooth feldspar or quartz crystal surface sections as well as intragranular pores. The site-specific deposition of colloids at intergranular pores is induced by small scale protrusions (mean height = 0.5 ± 0.3 μm). These protrusions diminish locally the overall DLVO interaction energy at the interface. The protrusions prevent further rolling over the surface by increasing the hydrodynamic drag required for detachment. Moreover, colloid sorption is favored at surface sections with high density of small protrusions (density (D) = 2.6 ± 0.55 μm(-1), asperity diameter (φ) = 0.6 ± 0.2 μm, height (h) = 0.4 ± 0.1 μm) in contrast to surface sections with larger asperities and lower asperity density (D = 1.2 ± 0.6 μm(-1), φ = 1.4 ± 0.4 μm, h = 0.6 ± 0.2 μm). The study elucidates the importance to include surface roughness parameters into predictive colloid-borne contaminant migration calculations.

  3. Synthesis and Applications of Non-spherical Dimer Colloids

    NASA Astrophysics Data System (ADS)

    Yoon, Kisun

    Colloids are promising building blocks in material synthesis because of their controllability of size and surface properties. The synthesis of chemically and/or geometrically anisotropic colloidal particles has received attentions with the expectation of building blocks for complex structures. However, the synthesis of anisotropic colloidal particles is by far more difficult than the synthesis of spherical colloidal particles. Lack of monodispersity and productivity of many anisotropic particles often limits their applications as a building block for complex structures. Thus, it is highly desirable to develop methods which can produce a large amount of monodisperse non-spherical particles with controllable asymmetric surface properties. This dissertation details the work for developing such a method. The major result of this dissertation is a synthetic method to produce monodisperse non-spherical colloids with anisotropic surface property in a large quantity. The anisotropic colloid, which we call it as Dimer particle, has two fused lobes like a dumbbell and each lobe's size can be independently controlled. We present a novel method to synthesize sub-micron size Dimer particles. This method can produce a large amount of submicron-sized Dimer particles with good monodispersity and well-controlled shape. Submicron-sized Dimer particles have been highly desired since they can be used as a building block for self assembly using Brownian motion, colloidal surfactant for Pickering emulsion, and photonic materials. To fully take advantage of the anisotropy of the particles, we develop a facile method to tailor the surface property of each lobe independently by asymmetrically coating the particles with gold nanoparticles. This method doesn't need the arrangement of particles onto any type of interfaces. Asymmetric coating of gold nanoparticles can be carried out simply by mixing Dimer particles with gold nanoparticles. The formation mechanism of the submicron-sized Dimer

  4. Sensitivity analyses of a colloid-facilitated contaminant transport model for unsaturated heterogeneous soil conditions.

    NASA Astrophysics Data System (ADS)

    Périard, Yann; José Gumiere, Silvio; Rousseau, Alain N.; Caron, Jean

    2013-04-01

    Certain contaminants may travel faster through soils when they are sorbed to subsurface colloidal particles. Indeed, subsurface colloids may act as carriers of some contaminants accelerating their translocation through the soil into the water table. This phenomenon is known as colloid-facilitated contaminant transport. It plays a significant role in contaminant transport in soils and has been recognized as a source of groundwater contamination. From a mechanistic point of view, the attachment/detachment of the colloidal particles from the soil matrix or from the air-water interface and the straining process may modify the hydraulic properties of the porous media. Šimůnek et al. (2006) developed a model that can simulate the colloid-facilitated contaminant transport in variably saturated porous media. The model is based on the solution of a modified advection-dispersion equation that accounts for several processes, namely: straining, exclusion and attachement/detachement kinetics of colloids through the soil matrix. The solutions of these governing, partial differential equations are obtained using a standard Galerkin-type, linear finite element scheme, implemented in the HYDRUS-2D/3D software (Šimůnek et al., 2012). Modeling colloid transport through the soil and the interaction of colloids with the soil matrix and other contaminants is complex and requires the characterization of many model parameters. In practice, it is very difficult to assess actual transport parameter values, so they are often calibrated. However, before calibration, one needs to know which parameters have the greatest impact on output variables. This kind of information can be obtained through a sensitivity analysis of the model. The main objective of this work is to perform local and global sensitivity analyses of the colloid-facilitated contaminant transport module of HYDRUS. Sensitivity analysis was performed in two steps: (i) we applied a screening method based on Morris' elementary

  5. A field study of colloid transport in surface and subsurface flows

    NASA Astrophysics Data System (ADS)

    Zhang, Wei; Tang, Xiang-Yu; Xian, Qing-Song; Weisbrod, Noam; Yang, Jae E.; Wang, Hong-Lan

    2016-11-01

    Colloids have been recognized to enhance the migration of strongly-sorbing contaminants. However, few field investigations have examined combined colloid transport via surface runoff and subsurface flows. In a headwater catchment of the upper Yangtze River, a 6 m (L) by 4 m (W) sloping (6°) farmland plot was built by cement walls to form no-flow side boundaries. The plot was monitored in the summer of 2014 for the release and transport of natural colloids via surface runoff and subsurface flows (i.e., the interflow from the soil-mudrock interface and fracture flow from the mudrock-sandstone interface) in response to rain events. The water sources of the subsurface flows were apportioned to individual rain events using a two end-member model (i.e., mobile pre-event soil water extracted by a suction-cup sampler vs. rainwater (event water)) based on δ18O measurements. For rain events with high preceding soil moisture, mobile pre-event soil water was the main contributor (generally >60%) to the fracture flow. The colloid concentration in the surface runoff was 1-2 orders of magnitude higher than that in the subsurface flows. The lowest colloid concentration was found in the subsurface interflow, which was probably the result of pore-scale colloid straining mechanisms. The rainfall intensity and its temporal variation govern the dynamics of the colloid concentrations in both surface runoff and subsurface flows. The duration of the antecedent dry period affected not only the relative contributions of the rainwater and the mobile pre-event soil water to the subsurface flows but also the peak colloid concentration, particularly in the fracture flow. The <10 μm fine colloid size fraction accounted for more than 80% of the total suspended particles in the surface runoff, while the colloid size distributions of both the interflow and the fracture flow shifted towards larger diameters. These results highlight the need to avoid the application of strongly

  6. 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

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. Enhanced colloidal stability of hydroxyapatite

    NASA Astrophysics Data System (ADS)

    Borum, La Rhonda Terese

    Hydroxyapatite, Ca10(PO4)6(OH) 2 is the most thermodynamically stable calcium phosphate in physiological environments. Hence, it is the main inorganic mineral found in bone and teeth. Its colloidal stability, however, is poor because hydroxyapatite (HAp) particles exhibit sediment formation upon standing at short time periods, where agglomerates form and lead to non-homogeneous suspensions. Surface modification is a promising method to tailor the colloidal stability of hydroxyapatite for biomaterial applications. Three techniques to modify the HAp surface and enhance the colloidal stability of HAp were investigated. Modified particles were characterized by methods sensitive to surface chemistry changes, such as sedimentation studies, diffuse reflectance Fourier transform infrared spectroscopy (DRIFT), Brunauer-Emmett-Teller (BET) surface area, and electrophoresis. Sedimentation studies demonstrated how effective each technique was in improving the colloidal stability of hydroxyapatite particles. Electrophoresis provided information on electrostatic interactions within each system. The first technique entailed an esterification reaction of the HAp surface with dodecyl alcohol at elevated temperatures. DRIFT results showed that dodecyl groups from the alcohol replaced acidic hydroxyl and phosphate sites on the HAp surface, giving rise to enhanced colloidal stability through steric interactions in ethanol suspensions. TGA curves gave insight to the degree of esterification for the esterified particles. Higher reaction temperatures give rise to a higher degree of esterification resulting in better colloidal stability. The second technique applied a silica coating on the HAp surface by the hydrolysis of tetraethyl orthosilicate in ethanol. Silica was coated onto the HAp surface at 5--75 wt% loading amounts. A combination of acid dissolution and x-ray diffraction (XRD), along with BET showed that the silica coating is complete at 50 wt% silica loading. The silica coating

  12. 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

  13. 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.

  14. Micro- and Nanotechnologies for Optical Neural Interfaces

    PubMed Central

    Pisanello, Ferruccio; Sileo, Leonardo; De Vittorio, Massimo

    2016-01-01

    In last decade, the possibility to optically interface with the mammalian brain in vivo has allowed unprecedented investigation of functional connectivity of neural circuitry. Together with new genetic and molecular techniques to optically trigger and monitor neural activity, a new generation of optical neural interfaces is being developed, mainly thanks to the exploitation of both bottom-up and top-down nanofabrication approaches. This review highlights the role of nanotechnologies for optical neural interfaces, with particular emphasis on new devices and methodologies for optogenetic control of neural activity and unconventional methods for detection and triggering of action potentials using optically-active colloidal nanoparticles. PMID:27013939

  15. Simulation of the self-assembly of colloidal droplets in a micro-channel

    NASA Astrophysics Data System (ADS)

    Ge, Zhouyang; Brandt, Luca

    2016-11-01

    In colloidal sciences, much progress has been made on the synthesis of complex building blocks mimicking molecular structures to elaborate innovative materials. The basic elements of such colloidal molecules are particles or droplets less than one millimeter in size. Their self-assembly relies on either lengthy brownian motion or careful microfludic designs, on top of typical colloidal interactions, e.g. depletion attraction. Regardless of the approach, however, questions remain why the colloids undergo certain path to organize themselves and how such process can be optimized. Here, we perform direct numerical simulations using a Navier-Stokes solver at low Reynolds number, combined with either the immersed boundary method (IBM) or a newly-proposed level set (LS) method for interface description. In the IBM simulations, the colloids are treated as rigid, spherical particles under a Lennard-Jones-like potential, reproducing attractive depletion force. Results show that, for four particles, a planar diamond is formed under a weak potential while a 3D tetrahedron is formed under a strong potential, which agree qualitatively with experiments. In the next step, LS simulation of colloidal droplets will be performed to investigate the roles of surface tension in the self-assembly. This project has received funding from the European Union's Horizon 2020 research and innovation programme under Grant agreement No 664823.

  16. Onset of anomalous diffusion in colloids confined to quasimonolayers

    NASA Astrophysics Data System (ADS)

    Bleibel, J.; Domínguez, Alvaro; Oettel, M.

    2017-03-01

    It has been recently shown that a colloidal monolayer, e.g., formed at a fluid interface or by means of a suitable confining potential, exhibits anomalous collective diffusion. This is a consequence of the hydrodynamic interactions mediated by the three-dimensional (3D) ambient fluid when the particles are confined to reside on a two-dimensional (2D) manifold. We study theoretically and with numerical simulations the crossover from normal to anomalous diffusion as the particles are, in real systems, confined by a 3D external potential and thus have the possibility to fluctuate out of the 2D manifold, thus forming a quasimonolayer.

  17. 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

  18. Colloid transport in unsaturated porous media: the role of water content and ionic strength on particle straining.

    PubMed

    Torkzaban, Saeed; Bradford, Scott A; van Genuchten, Martinus Th; Walker, Sharon L

    2008-02-19

    Packed column and mathematical modeling studies were conducted to explore the influence of water saturation, pore-water ionic strength, and grain size on the transport of latex microspheres (1.1 microm) in porous media. Experiments were carried out under chemically unfavorable conditions for colloid attachment to both solid-water interfaces (SWI) and air-water interfaces (AWI) using negatively charged and hydrophilic colloids and modifying the solution chemistry with a bicarbonate buffer to pH 10. Interaction energy calculations and complementary batch experiments were conducted and demonstrated that partitioning of colloids to the SWI and AWI was insignificant across the range of the ionic strengths considered. The breakthrough curve and final deposition profile were measured in each experiment indicating colloid retention was highly dependent on the suspension ionic strength, water content, and sand grain size. In contrast to conventional filtration theory, most colloids were found deposited close to the column inlet, and hyper-exponential deposition profiles were observed. A mathematical model, accounting for time- and depth-dependent straining, produced a reasonably good fit for both the breakthrough curves and final deposition profiles. Experimental and modeling results suggest that straining--the retention of colloids in low velocity regions of porous media such as grain junctions--was the primary mechanism of colloid retention under both saturated and unsaturated conditions. The extent of stagnant regions of flow within the pore structure is enhanced with decreasing water content, leading to a greater amount of retention. Ionic strength also contributes to straining, because the number of colloids that are held in the secondary energy minimum increases with ionic strength. These weakly associated colloids are prone to be translated to stagnation regions formed at grain-grain junctions, the solid-water-air triple point, and dead-end pores and then becoming

  19. Theory of the dynamics of evaporation-driven colloidal patterning

    NASA Astrophysics Data System (ADS)

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

    2014-03-01

    In the suspensions of colloidal particles in a volatile liquid film, deposits of the solute form near the contact line due to the flow generated by evaporation. An enticingly simple and experimentally realizable model system of this mechanism is the drying of a spilled drop of coffee on the countertop. Similarly, patterns of periodic bands or continuous solid films are commonly observed on a substrate suspended vertically in a container of the colloidal solution. In order to characterize these patterns, we develop a multiphase model that couples both the liquid and solid flows, local variation of the particle concentration, the propagation dynamics of the solid front, and the liquid-air interface deformation. For vertical liquid films, we further determine the nature of the filming-banding transition and the phase boundary in terms of the volume fraction of the colloids. The results of our theory are in good agreement with direct observations of these patterns. We gratefully acknowledge financial support from the Air Force Office of Scientific Research and the Kavli Institute for Bionano Science and Technology at Harvard University.

  20. Effects of Coalescence on Shear-Induced Gelation of Colloids.

    PubMed

    Jaquet, Baptiste; Lazzari, Stefano; Colonna, Luca; Colombo, Gabriele; Soos, Miroslav; Morbidelli, Massimo

    2017-02-07

    Shearing lyophobic colloidal suspensions can lead to aggregation, followed by gelation, if the formed clusters grow to sizes large enough to percolate. If the temperature is set over the glass transition temperature of the suspended material, the particles embedded in the same aggregate start to coalesce with one another. Coalescence occurs to the finite viscosity of the particles' material, which leads to material diffusion from particle to particle. The driving force of this process is the reduction of the particle-dispersant interface and, as a consequence, the decrease the center-to-center separation of the particles. This leads to decreased cluster size, and hence a delayed gelation. Simultaneously, coalescence reinforces the particle-particle bonds formed upon aggregation, leading to clusters that are able to resist higher hydrodynamic forces before breaking up, hence leading to faster gelation. These two competing effects, combined with the natural complexity of colloidal aggregation makes it rather difficult to understand and predict which trend becomes dominant. In the present work, the shear-induced gelation of model polymeric colloidal systems with different glass transition temperatures has been studied. Starting with their interaction potential we investigate the impact of temperature on the gel time in concentrated suspensions (φ = 5%) under steady shear, followed by the effect of temperature on the stress-resistance of fully destabilized clusters under agitation. The results of the present work allow for a systematic view and deepened understanding of the factors governing shear-induced gelation in the presence of coalescence.

  1. Colloid Straining within Saturated Heterogeneous Porous Media

    NASA Astrophysics Data System (ADS)

    Porubcan, A.; Walczak, J.; Xu, S.

    2008-12-01

    A thorough understanding of colloid movement in the subsurface system is critical to the assessment of groundwater pollution by pathogenic bacteria and colloid-bound contaminants. It is increasingly recognized that straining, a process that occurs when the pore space is too small to allow for a particle's passage, represents an important process in colloid immobilization within groundwater systems. Previously published studies have focused on the kinetics of colloid straining within sand packs composed of uniform mineral grains. Natural aquifers, however, are usually characterized by physically heterogeneous sediments. In this study, we conducted column transport experiments with carboxylated latex particles and quartz sand to investigate the impact of sediment texture (i.e., the size distribution of mineral grains) on colloid straining kinetics. The quartz sands used in the experiment were thoroughly cleaned and the strong repulsive interactions between colloid particles and quartz sands resulted in minimal physicochemical deposition so the straining kinetics can be quantified unambiguously. Sand packs of different textures were prepared by mixing sands of various sizes (mesh sizes of 20-25, 35-40 and 60-70). Our results suggested that the ratio of colloid size and the median sand grain size was insufficient to predict colloid straining within heterogeneous sediments. Soil texture, which was related to the size distribution of the sand grains, must be considered. A relationship between colloid straining kinetics and the heterogeneity of porous media that can be useful for the prediction of colloid transport within heterogeneous sediments was presented.

  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).

  3. Analytic studies of colloid transport in fractured porous media

    SciTech Connect

    Hwang, Y.; Chambre, P.L.; Lee, W.W.L.; Pigford, T.H.

    1989-11-01

    We analyze the interactive migration of radioactive colloids and solute in fractured rock. Two possible interactions between radionuclides as colloids and as solute are considered: solute sorption on nonradioactive colloids to form pseudocolloids, and dissolution of radioactive colloids. Previous studies have discussed the formation and transport of colloids in porous media, including removal of colloids by filtration and sedimentation. Colloids can migrate faster than solute because of weaker sorption on stationary solids and because of hydrochromatography of colloid particles in flow channels. However, the migration of colloids and pseudocolloids can be retarded by the interaction of colloids with solute, and the migration of solute in local equilibrium with colloids can be more rapid than if colloids were not present. Here we present a new quantative analysis to predict the interactive migration of colloids and solute in porous and fractured media. 4 figs.

  4. 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

  5. Designing Colloidal Molecules with Microfluidics

    PubMed Central

    Shen, Bingqing; Ricouvier, Joshua; Malloggi, Florent

    2016-01-01

    The creation of new colloidal materials involves the design of functional building blocks. Here, a microfluidic method for designing building blocks one by one, at high throughput, with a broad range of shapes is introduced. The method exploits a coupling between hydrodynamic interactions and depletion forces that controls the configurational dynamics of droplet clusters traveling in microfluidic channels. Droplet clusters can be solidified in situ with UV. By varying the flow parameters, clusters are prescribed a given size, geometry, chemical and/or magnetic heterogeneities enabling local bonding. Compact structures (chains, triangles, diamonds, tetrahedrons,...) and noncompact structures, such as crosses and T, difficult to obtain with current techniques are produced. Size dispersions are small (2%) and throughputs are high (30 000 h−1). The work opens a new pathway, based on microfluidics, for designing colloidal building blocks with a potential to enable the creation of new materials. PMID:27840804

  6. Biaxial ferromagnetic liquid crystal colloids

    PubMed Central

    Liu, Qingkun; Ackerman, Paul J.; Lubensky, Tom C.; Smalyukh, Ivan I.

    2016-01-01

    The design and practical realization of composite materials that combine fluidity and different forms of ordering at the mesoscopic scale are among the grand fundamental science challenges. These composites also hold a great potential for technological applications, ranging from information displays to metamaterials. Here we introduce a fluid with coexisting polar and biaxial ordering of organic molecular and magnetic colloidal building blocks exhibiting the lowest symmetry orientational order. Guided by interactions at different length scales, rod-like organic molecules of this fluid spontaneously orient along a direction dubbed “director,” whereas magnetic colloidal nanoplates order with their dipole moments parallel to each other but pointing at an angle to the director, yielding macroscopic magnetization at no external fields. Facile magnetic switching of such fluids is consistent with predictions of a model based on competing actions of elastic and magnetic torques, enabling previously inaccessible control of light. PMID:27601668

  7. Predicting crystals of Janus colloids

    NASA Astrophysics Data System (ADS)

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

    2013-04-01

    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.

  8. Visualizing the Analogy between Competitive Adsorption and Colloid Stability to Restore Lung Surfactant Function

    PubMed Central

    Shieh, Ian C.; Waring, Alan J.; Zasadzinski, Joseph A.

    2012-01-01

    We investigated a model of acute respiratory distress syndrome in which the serum protein albumin adsorbs to an air-liquid interface and prevents the thermodynamically preferable adsorption of the clinical lung surfactant Survanta by inducing steric and electrostatic energy barriers analogous to those that prevent colloidal aggregation. Chitosan and polyethylene glycol (PEG), two polymers that traditionally have been used to aggregate colloids, both allow Survanta to quantitatively displace albumin from the interface, but through two distinct mechanisms. Direct visualization with confocal microscopy shows that the polycation chitosan coadsorbs to interfacial layers of both Survanta and albumin, and also colocalizes with the anionic domains of Survanta at the air-liquid interface, consistent with it eliminating the electrostatic repulsion by neutralizing the surface charges on albumin and Survanta. In contrast, the PEG distribution does not change during the displacement of albumin by Survanta, consistent with PEG inducing a depletion attraction sufficient to overcome the repulsive energy barrier toward adsorption. PMID:22385848

  9. Thermophoresis of charged colloidal particles.

    PubMed

    Fayolle, Sébastien; Bickel, Thomas; Würger, Alois

    2008-04-01

    Thermally induced particle flow in a charged colloidal suspension is studied in a fluid-mechanical approach. The force density acting on the charged boundary layer is derived in detail. From Stokes' equation with no-slip boundary conditions at the particle surface, we obtain the particle drift velocity and the thermophoretic transport coefficients. The results are discussed in view of previous work and available experimental data.

  10. Three-dimensional colloidal lithography.

    PubMed

    Nagai, Hironori; Poteet, Austen; Zhang, Xu A; Chang, Chih-Hao

    2017-03-24

    Light interactions with colloidal particles can generate a variety of complex three-dimensional (3D) intensity patterns, which can be utilized for nanolithography. The study of particle-light interactions can add more types of intensity patterns by manipulating key factors. Here we investigate a novel 3D nanolithography technique using colloidal particles under two-beam coherent illuminations. The fabricated 3D nanostructures are hollow, nested within periodic structures, and possess multiple chamber geometry. The effects of incident angles and particle size on the fabricated nanostructures were examined. The relative phase shift between particle position and interference pattern is identified as another significant parameter influencing the resultant nanostructures. A numerical model has been developed to show the evolution of nanostructure geometry with phase shifts, and experimental studies confirm the simulation results. Through the introduction of single colloidal particles, the fabrication capability of Lloyd's mirror interference can now be extended to fabrication of 3D nanostructure with complex shell geometry. The fabricated hollow nanostructures with grating background could find potential applications in the area of photonics, drug delivery, and nanofluidics.

  11. Three-dimensional colloidal lithography

    NASA Astrophysics Data System (ADS)

    Nagai, Hironori; Poteet, Austen; Zhang, Xu A.; Chang, Chih-Hao

    2017-03-01

    Light interactions with colloidal particles can generate a variety of complex three-dimensional (3D) intensity patterns, which can be utilized for nanolithography. The study of particle–light interactions can add more types of intensity patterns by manipulating key factors. Here we investigate a novel 3D nanolithography technique using colloidal particles under two-beam coherent illuminations. The fabricated 3D nanostructures are hollow, nested within periodic structures, and possess multiple chamber geometry. The effects of incident angles and particle size on the fabricated nanostructures were examined. The relative phase shift between particle position and interference pattern is identified as another significant parameter influencing the resultant nanostructures. A numerical model has been developed to show the evolution of nanostructure geometry with phase shifts, and experimental studies confirm the simulation results. Through the introduction of single colloidal particles, the fabrication capability of Lloyd’s mirror interference can now be extended to fabrication of 3D nanostructure with complex shell geometry. The fabricated hollow nanostructures with grating background could find potential applications in the area of photonics, drug delivery, and nanofluidics.

  12. Overview: Experimental studies of crystal nucleation: Metals and colloids

    NASA Astrophysics Data System (ADS)

    Herlach, Dieter M.; Palberg, Thomas; Klassen, Ina; Klein, Stefan; Kobold, Raphael

    2016-12-01

    Crystallization is one of the most important phase transformations of first order. In the case of metals and alloys, the liquid phase is the parent phase of materials production. The conditions of the crystallization process control the as-solidified material in its chemical and physical properties. Nucleation initiates the crystallization of a liquid. It selects the crystallographic phase, stable or meta-stable. Its detailed knowledge is therefore mandatory for the design of materials. We present techniques of containerless processing for nucleation studies of metals and alloys. Experimental results demonstrate the power of these methods not only for crystal nucleation of stable solids but in particular also for investigations of crystal nucleation of metastable solids at extreme undercooling. This concerns the physical nature of heterogeneous versus homogeneous nucleation and nucleation of phases nucleated under non-equilibrium conditions. The results are analyzed within classical nucleation theory that defines the activation energy of homogeneous nucleation in terms of the interfacial energy and the difference of Gibbs free energies of solid and liquid. The interfacial energy acts as barrier for the nucleation process. Its experimental determination is difficult in the case of metals. In the second part of this work we therefore explore the potential of colloidal suspensions as model systems for the crystallization process. The nucleation process of colloids is observed in situ by optical observation and ultra-small angle X-ray diffraction using high intensity synchrotron radiation. It allows an unambiguous discrimination of homogeneous and heterogeneous nucleation as well as the determination of the interfacial free energy of the solid-liquid interface. Our results are used to construct Turnbull plots of colloids, which are discussed in relation to Turnbull plots of metals and support the hypothesis that colloids are useful model systems to investigate crystal

  13. 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

  14. Nanostructured colloidal crystals from forced hydrolysis methods.

    PubMed

    Otal, Eugenio H; Granada, Mara; Troiani, Horacio E; Cánepa, Horacio; Walsöe de Reca, Noemí E

    2009-08-18

    In this work, an original route for ZnO nanostructured spherical colloids and their assembly into colloidal crystals are presented. The temporal evolution of crystal size and shape was followed by X-ray diffraction and the colloids size distribution by scanning electron microscopy. These spherical colloids showed a change in their size dispersion with aging time. Early stage suspensions, with a narrow size distribution, were settled to the bottom and dried with a slow evaporation rate to obtain colloidal crystals. This original route provides a new material for future applications in opalline photonic crystals, with a dielectric constant higher than that of classical materials (silica and latex). Moreover, this route means an improvement of previously reported data from the literature since it involves a one-pot strategy and room-temperature colloid assembly.

  15. Crystallization of DNA-coated colloids

    NASA Astrophysics Data System (ADS)

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

    2015-06-01

    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.

  16. Colloidal polycrystalline monolayers under oscillatory shear

    NASA Astrophysics Data System (ADS)

    Buttinoni, Ivo; Steinacher, Mathias; Spanke, Hendrik Th.; Pokki, Juho; Bahmann, Severin; Nelson, Bradley; Foffi, Giuseppe; Isa, Lucio

    2017-01-01

    In this paper we probe the structural response to oscillatory shear deformations of polycrystalline monolayers of soft repulsive colloids with varying area fraction over a broad range of frequencies and amplitudes. The particles are confined at a fluid interface, sheared using a magnetic microdisk, and imaged through optical microscopy. The structural and mechanical response of soft materials is highly dependent on their microstructure. If crystals are well understood and deform through the creation and mobilization of specific defects, the situation is much more complex for disordered jammed materials, where identifying structural motifs defining plastically rearranging regions remains an elusive task. Our materials fall between these two classes and allow the identification of clear pathways for structural evolution. In particular, we demonstrate that large enough strains are able to fluidize the system, identifying critical strains that fulfill a local Lindemann criterion. Conversely, smaller strains lead to localized and erratic irreversible particle rearrangements due to the motion of structural defects. In this regime, oscillatory shear promotes defect annealing and leads to the growth of large crystalline domains. Numerical simulations help identify the population of rearranging particles with those exhibiting the largest deviatoric stresses and indicate that structural evolution proceeds towards the minimization of the stress stored in the system. The particles showing high deviatoric stresses are localized around grain boundaries and defects, providing a simple criterion to spot regions likely to rearrange plastically under oscillatory shear.

  17. Dynamic Colloidal Stabilization by Nanoparticle Halos

    NASA Astrophysics Data System (ADS)

    Karanikas, S.; Louis, A. A.

    2004-12-01

    We explore the conditions under which colloids can be stabilized by the addition of smaller particles. The largest repulsive barriers between colloids occur when the added particles repel each other with soft interactions, leading to an accumulation near the colloid surfaces. At lower densities these layers of mobile particles (nanoparticle halos) result in stabilization, but when too many are added, the interactions become attractive again. We systematically study these effects—accumulation repulsion, reentrant attraction, and bridging—by accurate integral equation techniques.

  18. Transformative Colloidal Nanomaterials for Mid- Infrared Devices

    DTIC Science & Technology

    2015-06-11

    SECURITY CLASSIFICATION OF: The grant focused on the Photoluminescence efficiency of HgTe colloidal quantum dots. The photoluminescence quantum yield...of HgTe colloidal quantum dots was measured from 1800 to 6500 cm-1 . There is a steep drop at low energy consistent with the generic gap law...Distribution Unlimited Final Report: Transformative Colloidal Nanomaterials for Mid- Infrared Devices The views, opinions and/or findings contained in this

  19. 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.

  20. Thermophoresis of colloids by mesoscale simulations.

    PubMed

    Lüsebrink, Daniel; Yang, Mingcheng; Ripoll, Marisol

    2012-07-18

    The motion of a colloid induced by a temperature gradient is simulated by means of multiparticle collision dynamics, a mesoscale simulation technique. Two algorithms to quantify the thermophoretic behavior are employed and contrasted. The validity of the methods is verified as a function of the temperature gradient, system size, and algorithm parameters. The variation of the solvent-colloid interaction from attractive to purely repulsive interestingly results in the change of the colloid behavior from thermophobic to thermophilic.

  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. The role of ionic strength and grain size on the transport of colloids in unsaturated sand columns

    NASA Astrophysics Data System (ADS)

    Mitropoulou, Polyxeni N.; Syngouna, Vasiliki I.; Chrysikopoulos, Constantinos V.

    2013-04-01

    The main objective of this study was to better understand the combined effects of ionic strength, and sand grain size on colloid fate and transport in unsaturated porous media. Spherical fluorescent polymer microspheres with three different sizes (0.075, 0.30 and 2.1 μm), and laboratory columns packed with two size fractions of clean quartz sand (0.513 and 0.181 mm) were used. The saturation level of the packed columns was set to 83-95% with solutions having a wide range of ionic strength (0.1-1000 mM). The electrophoretic mobility of colloids and sand grains were evaluated for all the experimental conditions employed. The various experimental collision efficiencies were quantified using the classical colloid filtration theory. The theoretical collision efficiencies were estimated with appropriate DLVO energies using a Maxwell model. The experimental results suggested that the retention of the bigger colloids (2.1 μm) was slightly higher compared to the conservative tracer and smaller colloids (0.3 and 0.075 μm) in deionized-distilled-water, indicating sorption at air-water interfaces or straining. Moreover, relatively smaller attachment was observed onto fine than medium quartz sand. The mass recovery of the 0.3 μm microspheres in NaCl solution was shown to significantly decrease with increasing ionic strength. Both the experimental and theoretical collision efficiencies based on colloid interactions with solid-water interfaces, were increased with increasing ionic strength.

  3. Grain-boundary fluctuations in two-dimensional colloidal crystals.

    PubMed

    Skinner, Thomas O E; Aarts, Dirk G A L; Dullens, Roel P A

    2010-10-15

    We study grain-boundary fluctuations in two-dimensional colloidal crystals in real space and time using video microscopy. The experimentally obtained static and dynamic correlation functions are very well described by expressions obtained using capillary wave theory. This directly leads to values for the interfacial stiffness and the interface mobility, the key parameters in curvature-driven grain-boundary migration. Furthermore, we show that the average grain-boundary position exhibits a one-dimensional random walk as recently suggested by computer simulations [Z. T. Trautt, M. Upmanyu, and A. Karma, Science 314, 632 (2006)]. The interface mobility determined from the mean-square displacement of the average grain-boundary position is in good agreement with values inferred from grain-boundary fluctuations.

  4. 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)

  5. 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.

  6. 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.

  7. Analysis on laser plasma emission for characterization of colloids by video-based computer program

    NASA Astrophysics Data System (ADS)

    Putri, Kirana Yuniati; Lumbantoruan, Hendra Damos; Isnaeni

    2016-02-01

    Laser-induced breakdown detection (LIBD) is a sensitive technique for characterization of colloids with small size and low concentration. There are two types of detection, optical and acoustic. Optical LIBD employs CCD camera to capture the plasma emission and uses the information to quantify the colloids. This technique requires sophisticated technology which is often pricey. In order to build a simple, home-made LIBD system, a dedicated computer program based on MATLAB™ for analyzing laser plasma emission was developed. The analysis was conducted by counting the number of plasma emissions (breakdowns) during a certain period of time. Breakdown probability provided information on colloid size and concentration. Validation experiment showed that the computer program performed well on analyzing the plasma emissions. Optical LIBD has A graphical user interface (GUI) was also developed to make the program more user-friendly.

  8. Transport and crystallization of colloidal particles in a thin nematic cell

    NASA Astrophysics Data System (ADS)

    Karabot, M. Å.; Tkalec, U.; Muševič, I.

    2007-09-01

    In a thin planar nematic cell, the application of an AC electric field induces a macroscopic transport of micrometer-sized colloidal particles along the nematic director. We have analyzed the dependence of particle velocities on the electric-field amplitude and frequency and found that it decreases exponentially with increasing frequency. Using specially designed electrodes we have observed that colloidal particles could be pumped and accelerated across the field-no-field interface, and measured the structural force and the corresponding potential, which is of the order of 10000 kBT for 4μm particles. We demonstrate that spatially periodic close-packed crystalline colloidal structures can be obtained, which are thermodinamically metastable for many days after turning off the electric field and slowly decay into linear chains. Above the nematic-isotropic phase transition, such crystalline structures are non-stable and decay in few minutes.

  9. Colloid transport in dual-permeability media.

    PubMed

    Leij, Feike J; Bradford, Scott A

    2013-07-01

    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 increased risks for disease caused by microorganisms and colloid-associated contaminants. This study presents a model for colloid transport in dual-permeability media that includes reversible and irreversible retention of colloids and first-order exchange between the aqueous phases of the two regions. The model may also be used to describe transport of other reactive solutes in dual-permeability media. Analytical solutions for colloid concentrations in aqueous and solid phases were obtained using Laplace transformation and matrix decomposition. The solutions proved convenient to assess the effect of model parameters on the colloid distribution. The analytical model was used to describe effluent concentrations for a bromide tracer and 3.2- or 1-μm-colloids that were observed after transport through a composite 10-cm long porous medium made up of a cylindrical lens or core of sand and a surrounding matrix with sand of a different grain size. The tracer data were described very well and realistic estimates were obtained for the pore-water velocity in the two flow domains. An accurate description was also achieved for most colloid breakthrough curves. Dispersivity and retention parameters were typically greater for the larger 3.2-μm-colloids while both reversible and irreversible retention rates tended to be higher for the finer sands than the coarser sand. The relatively small sample size and the complex flow pattern in the composite medium made it difficult to reach definitive conclusions regarding transport parameters for colloid transport.

  10. The hydrodynamics of colloidal gelation.

    PubMed

    Varga, Zsigmond; Wang, Gang; Swan, James

    2015-12-14

    Colloidal gels are formed during arrested phase separation. Sub-micron, mutually attractive particles aggregate to form a system spanning network with high interfacial area, far from equilibrium. Models for microstructural evolution during colloidal gelation have often struggled to match experimental results with long standing questions regarding the role of hydrodynamic interactions. In nearly all models, these interactions are neglected entirely. In the present work, we report simulations of gelation with and without hydrodynamic interactions between the suspended particles executed in HOOMD-blue. The disparities between these simulations are striking and mirror the experimental-theoretical mismatch in the literature. The hydrodynamic simulations agree with experimental observations, however. We explore a simple model of the competing transport processes in gelation that anticipates these disparities, and conclude that hydrodynamic forces are essential. Near the gel boundary, there exists a competition between compaction of individual aggregates which suppresses gelation and coagulation of aggregates which enhances it. The time scale for compaction is mildly slowed by hydrodynamic interactions, while the time scale for coagulation is greatly accelerated. This enhancement to coagulation leads to a shift in the gel boundary to lower strengths of attraction and lower particle concentrations when compared to models that neglect hydrodynamic interactions. Away from the gel boundary, differences in the nearest neighbor distribution and fractal dimension persist within gels produced by both simulation methods. This result necessitates a fundamental rethinking of how dynamic, discrete element models for gelation kinetics are developed as well as how collective hydrodynamic interactions influence the arrest of attractive colloidal dispersions.

  11. Patchy particles using colloidal caps

    NASA Astrophysics Data System (ADS)

    Middleton, Christine; Pine, David

    2015-03-01

    We present a method for making patchy particles functionalized with single stranded sticky end DNA only on their patches. This is done by adding ``spherical cap'' particles as patches to spherical colloids using the depletion interaction. The caps are then functionalized with single stranded DNA using copper-free click chemistry. Due to being attached only by depletion, the patches diffuse on the surface of the particle. The patchy particles can then interact with each other in a specific, directional way through the mobile, DNA functionalized patches.

  12. Corralled Colloids in Four Dimensions

    NASA Astrophysics Data System (ADS)

    Anthony, Stephen; Kim, Minsu; Granick, Steve

    2008-03-01

    Three colloidal particles were placed in small corrals and the strong correlations between their translation and rotation were quantified using the optical anisotropy of MOON (Modulated Optical Nanoprobes) particles to simultaneously measure their translation and rotation in an optical microscope. This system represents the simplest system which can capture one of the relevant components of multi-body interactions, the fact that while two particles can freely rotate together (like gears), once a third particle (or gear) is added there is no universally favorable set of rotations. This simple multi-body system provides a paradigm of how rotation influences translation and vice-versa.

  13. 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)

  14. 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..

  15. 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...

  16. Interfacial undercooling in solidification of colloidal suspensions: analyses with quantitative measurements

    PubMed Central

    You, Jiaxue; Wang, Lilin; Wang, Zhijun; Li, Junjie; Wang, Jincheng; Lin, Xin; Huang, Weidong

    2016-01-01

    Interfacial undercooling in the complex solidification of colloidal suspensions is of significance and remains a puzzling problem. Two types of interfacial undercooling are supposed to be involved in the freezing of colloidal suspensions, i.e., solute constitutional supercooling (SCS) caused by additives in the solvent and particulate constitutional supercooling (PCS) caused by particles. However, quantitative identification of the interfacial undercooling in the solidification of colloidal suspensions, is still absent; thus, the question of which type of undercooling is dominant in this complex system remains unanswered. Here, we quantitatively measured the static and dynamic interface undercoolings of SCS and PCS in ideal and practical colloidal systems. We show that the interfacial undercooling primarily comes from SCS caused by the additives in the solvent, while PCS is minor. This finding implies that the thermodynamic effect of particles from the PCS is not the fundamental physical mechanism for pattern formation of cellular growth and lamellar structure in the solidification of colloidal suspensions, a general case of ice-templating method. Instead, the patterns in the ice-templating method can be controlled effectively by adjusting the additives. PMID:27329394

  17. Interface engineering in inorganic hybrid structures towards improved photocatalysis (Conference Presentation)

    NASA Astrophysics Data System (ADS)

    Xiong, Yujie

    2016-10-01

    Designing new photocatalytic materials for improving photoconversion efficiency is a promising route to alleviate the steadily worsening environmental issues and energy crisis. Despite the invention of a large number of catalytic materials with well-defined structures, their overall efficiency in photocatalysis is still quite limited as the three key steps - light harvesting, charge generation and separation, and charge transfer to surface for redox reactions - have not been substantially improved. To improve each step in the complex process, there is a major trend to develop materials based on inorganic hybrid structures. In this case, interface engineering holds the promise for boosting the overall efficiency, given the key roles of interface structures in charge and energy transfer. In this talk, I will demonstrate several different approaches to designing inorganic hybrid structures with improved photocatalytic performance via interface engineering. The typical demonstrations include semiconductor-plasmonics systems for broad-spectrum light harvesting, metal-semiconductor interfaces for improved charge separation, semiconductor-MOF (metal-organic framework) configurations for activated surface reactions. It is anticipated that this series of works open a new window to rationally designing inorganic hybrid materials for photo-induced applications. References: (1) Bai, S.; Yang, L.; Wang, C.; Lin, Y.; Lu, J.; Jiang, J. and Xiong, Y.*, Angew. Chem. Int. Ed. 54, 14810-14814 (2015). (2) Bai, S.; Jiang, J.; Zhang, Q. and Xiong, Y.*, Chem. Soc. Rev. 44, 2893-2939 (2015). (3) Bai, S.; Li, X.; Kong, Q.; Long, R.; Wang, C.; Jiang, J. and Xiong, Y.*, Adv. Mater. 27, 3444-3452 (2015). (4) Bai, S.; Ge, J.; Wang, L.; Gong, M.; Deng, M.; Kong, Q.; Song, L.; Jiang, J.;* Zhang, Q.;* Luo, Y.; Xie, Y. and Xiong, Y.*, Adv. Mater. 26, 5689-5695 (2014). (5) Li, R.; Hu, J.; Deng, M.; Wang, H.; Wang, X.; Hu, Y.; Jiang, H. L.; Jiang, J.;* Zhang, Q.;* Xie, Y. and Xiong, Y.*, Adv. Mater

  18. Structural transitions in condensed colloidal virus phases

    NASA Astrophysics Data System (ADS)

    Schmidt, Nathan; Barr, Steve; Udit, Andrew; Gutierrez, Leonardo; Nguyen, Thanh; Finn, M. G.; Luijten, Erik; Wong, Gerard

    2010-03-01

    Analogous to monatomic systems colloidal phase behavior is entirely determined by the interaction potential between particles. This potential can be tuned using solutes such as multivalent salts and polymers with varying affinity for the colloids to create a hierarchy of attractions. Bacteriophage viruses are a naturally occurring type of colloidal particle with characteristics difficult to achieve by laboratory synthesis. They are monodisperse, nanometers in size, and have heterogeneous surface charge distributions. We use the MS2 and Qbeta bacteriophages (diameters 27-28nm) to understand the interplay between different attraction mechanisms on nanometer-sized colloids. Small Angle X-ray Scattering (SAXS) is used to characterize the inter-particle interaction between colloidal viruses using several polymer species and different salt types.

  19. Optical effects of charges in colloidal solutions

    NASA Astrophysics Data System (ADS)

    Chang, Railing; Chung, Hung-Yi; Chen, Chih-Wei; Chiang, Hai-Pang; Leung, P. T.

    2017-04-01

    The optical response of charged polymeric and metallic colloids is investigated using effective medium theories for composite systems of nanoparticles. Based on the Bohren-Hunt theory for generalized Mie scattering from charged particles, an effective quasi-static dielectric function previously obtained is applied to the present study to characterize the response from the various colloidal particles. It is found that such effects are more prominent for polymeric and nonmetallic colloidal solutions in general. In addition, the effects of clustering among the colloidal particles are also studied via a fractal model available from the literature. Detailed numerical studies of the dependence of these effects on the amount of extraneous charge, as well as on the geometry and volume fraction of the colloidal particles are presented.

  20. Pickering emulsions stabilized by oppositely charged colloids: Stability and pattern formation

    NASA Astrophysics Data System (ADS)

    Christdoss Pushpam, Sam David; Basavaraj, Madivala G.; Mani, Ethayaraja

    2015-11-01

    A binary mixture of oppositely charged colloids can be used to stabilize water-in-oil or oil-in-water emulsions. A Monte Carlo simulation study to address the effect of charge ratio of colloids on the stability of Pickering emulsions is presented. The colloidal particles at the interface are modeled as aligned dipolar hard spheres, with attractive interaction between unlike-charged and repulsive interaction between like-charged particles. The optimum composition (fraction of positively charged particles) required for the stabilization corresponds to a minimum in the interaction energy per particle. In addition, for each charge ratio, there is a range of compositions where emulsions can be stabilized. The structural arrangement of particles or the pattern formation at the emulsion interface is strongly influenced by the charge ratio. We find well-mixed isotropic, square, and hexagonal arrangements of particles on the emulsion surface for different compositions at a given charge ratio. The distribution of coordination numbers is calculated to characterize structural features. The simulation study is useful for the rational design of Pickering emulsifications wherein oppositely charged colloids are used, and for the control of pattern formation that can be useful for the synthesis of colloidosomes and porous shells derived thereof.

  1. Mechanistic principles of colloidal crystal growth by evaporation-induced convective steering.

    PubMed

    Brewer, Damien D; Allen, Joshua; Miller, Michael R; de Santos, Juan M; Kumar, Satish; Norris, David J; Tsapatsis, Michael; Scriven, L E

    2008-12-02

    We simulate evaporation-driven self-assembly of colloidal crystals using an equivalent network model. Relationships between a regular hexagonally close-packed array of hard, monodisperse spheres, the associated pore space, and selectivity mechanisms for face-centered cubic microstructure propagation are described. By accounting for contact line rearrangement and evaporation at a series of exposed menisci, the equivalent network model describes creeping flow of solvent into and through a rigid colloidal crystal. Observations concerning colloidal crystal growth are interpreted in terms of the convective steering hypothesis, which posits that solvent flow into and through the pore space of the crystal may play a major role in colloidal self-assembly. Aspects of the convective steering and deposition of high-Peclet-number rigid spherical particles at a crystal boundary are inferred from spatially resolved solvent flow into the crystal. Gradients in local flow through boundary channels were predicted due to the channels' spatial distribution relative to a pinned free surface contact line. On the basis of a uniform solvent and particle flux as the criterion for stability of a particular growth plane, these network simulations suggest the stability of a declining {311} crystal interface, a symmetry plane which exclusively propagates fcc microstructure. Network simulations of alternate crystal planes suggest preferential growth front evolution to the declining {311} interface, in consistent agreement with the proposed stability mechanism for preferential fcc microstructure propagation in convective assembly.

  2. Colloid Transport and Retention in Fractured Media

    SciTech Connect

    McCarthy, J.F.

    2001-02-01

    The goal of this project was to identify the chemical and physical factors that control the transport of colloids in fractured materials, and develop a generalized capability to predict colloid attachment and detachment based on hydraulic factors (head, flow rate), physical processes and structure (fracture aperture, matrix porosity), and chemical properties (surface properties of colloids, solution chemistry, and mineralogy of fracture surfaces). Both aqueous chemistry and physical structure of geologic formations influenced transport. Results of studies at all spatial scales reached consensus on the importance of several key controlling variables: (1) colloid retention is dominated by chemical conditions favoring colloid-wall interactions; (2) even in the presence of conditions favorable to colloid collection, deposited colloids are remobilized over long times and this process contributes substantially to the overall extent of transport; (3) diffusive exchange between water-conducting fractures and finer fractures and pores acts to ''buffer'' the effects of the major fracture network structure, and reduces predictive uncertainties. Predictive tools were developed that account for fundamental mechanisms of colloid dynamics in fracture geometry, and linked to larger-scale processes in networks of fractures. The results of our study highlight the key role of physical and hydrologic factors, and processes of colloid remobilization that are potentially of even greater importance to colloid transport in the vadose zone than in saturated conditions. We propose that this work be extended to focus on understanding vadose zone transport processes so that they can eventually be linked to the understanding and tools developed in our previous project on transport in saturated groundwater systems.

  3. Gel trapping of dense colloids.

    PubMed

    Laxton, Peter B; Berg, John C

    2005-05-01

    Phase density differences in sols, foams, or emulsions often lead to sedimentation or creaming, causing problems for materials where spatial uniformity over extended periods of time is essential. The problem may be addressed through the use of rheology modifiers in the continuous phase. Weak polymer gels have found use for this purpose in the food industry where they appear to be capable of trapping dispersoid particles in a three-dimensional matrix while displaying water-like viscosities at low shear. Attempts to predict sedimentation stability in terms of particle properties (size, shape, density difference) and gel yield stress have led to qualitative success for suspensions of large particles. The effect of particle size, however, in particular the case in which colloidal dimensions are approached, has not been investigated. The present work seeks to determine useful stability criteria for colloidal dispersions in terms of readily accessible viscoelastic descriptors. Results are reported for systems consisting of 12 microm poly(methyl methacrylate) (PMMA) spheres dispersed in aqueous gellan gum. Monovalent salt concentration is varied to control rheological properties, and sedimentation/centrifugation experiments are performed to determine dispersion stability. Necessary conditions for stability consist of a minimum yield stress together with a value of tan delta less than unity.

  4. 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.

  5. 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

  6. Recent Advances in Colloidal and Interfacial Phenomena Involving Liquid Crystals

    PubMed Central

    Bai, Yiqun; Abbott, Nicholas L.

    2011-01-01

    This article describes recent advances in several areas of research involving the interfacial ordering of liquid crystals (LCs). The first advance revolves around the ordering of LCs at bio/chemically functionalized surfaces. Whereas the majority of past studies of surface-induced ordering of LCs have involved surfaces of solids that present a limited diversity of chemical functional groups (surfaces at which van der Waals forces dominate surface-induced ordering), recent studies have moved to investigate the ordering of LCs on chemically complex surfaces. For example, surfaces decorated with biomolecules (e.g. oligopeptides and proteins) and transition metal ions have been investigated, leading to an understanding of the roles that metal-ligand coordination interactions, electrical double-layers, acid-base interactions, and hydrogen bonding can have on the interfacial ordering of LCs. The opportunity to create chemically-responsive LCs capable of undergoing ordering transitions in the presence of targeted molecular events (e.g., ligand exchange around a metal center) has emerged from these fundamental studies. A second advance has focused on investigations of the ordering of LCs at interfaces with immiscible isotropic fluids, particularly water. In contrast to prior studies of surface-induced ordering of LCs on solid surfaces, LC- aqueous interfaces are deformable and molecules at these interfaces exhibit high levels of mobility and thus can reorganize in response to changes in interfacial environment. A range of fundamental investigations involving these LC-aqueous interfaces have revealed that (i) the spatial and temporal characteristics of assemblies formed from biomolecular interactions can be reported by surface-driven ordering transitions in the LCs, (ii) the interfacial phase behaviour of molecules and colloids can be coupled to (and manipulated via) the ordering (and nematic elasticity) of LCs, and (iii) confinement of LCs leads to unanticipated size

  7. 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

  8. A generalized description of aquatic colloidal interactions: The three-colloidal component approach

    SciTech Connect

    Buffle, J.; Wilkinson, K.J.; Stoll, S.; Filella, M.; Zhang, J.

    1998-10-01

    This paper describes several possible interactions among the different types of organic and inorganic aquatic colloids, based on present knowledge of their size, electric charge, and conformation. The physico-chemical properties of the different groups of colloids are described. Emphasis is placed on the various types of organic components, including fulvic compounds. Subsequently, the role of each colloid class is discussed with respect to homoaggregation (aggregation within a given colloid class) and heteroaggregation (aggregation among different colloid types). On the basis of a synthesis of literature reports, microscopic observations of natural colloids, experimental results obtained with model systems, and numerical simulations, it is concluded that the formation of aggregates in aquatic systems can be understood by mainly considering the roles of three types of colloids: (1) compact inorganic colloids; (2) large, rigid biopolymers; and (3) either the soil-derived fulvic compounds or their equivalent in pelagic waters, aquagenic refractory organic matter. In most natural aquatic systems, the small fulvic compounds will stabilize the inorganic colloids whereas the rigid biopolymers will destabilize them. The concentration of stable colloids in a particular aquatic system will depend on the relative proportions of these three components.

  9. Fluid-fluid demixing curves for colloid-polymer mixtures in a random colloidal matrix

    NASA Astrophysics Data System (ADS)

    Annunziata, Mario Alberto; Pelissetto, Andrea

    2011-12-01

    We study fluid-fluid phase separation in a colloid-polymer mixture adsorbed in a colloidal porous matrix close to the θ point. For this purpose we consider the Asakura-Oosawa model in the presence of a quenched matrix of colloidal hard spheres. We study the dependence of the demixing curve on the parameters that characterize the quenched matrix, fixing the polymer-to-colloid size ratio to 0.8. We find that, to a large extent, demixing curves depend only on a single parameter f, which represents the volume fraction which is unavailable to the colloids. We perform Monte Carlo simulations for volume fractions f equal to 40% and 70%, finding that the binodal curves in the polymer and colloid packing-fraction plane have a small dependence on disorder. The critical point instead changes significantly: for instance, the colloid packing fraction at criticality increases with increasing f. Finally, we observe for some values of the parameters capillary condensation of the colloids: a bulk colloid-poor phase is in chemical equilibrium with a colloid-rich phase in the matrix.

  10. 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.

  11. 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.

  12. Photochemical manipulation of colloidal structures in liquid-crystal colloids

    NASA Astrophysics Data System (ADS)

    Yamamoto, T.; Tabe, Y.; Yokoyama, H.

    2007-05-01

    We investigated photochemical manipulation of physical properties and colloidal structures in liquid-crystal (LC) colloids containing azobenzene compounds. In a LC suspension where polymeric particles were dispersed in a host LC, we achieved photochemical control of light-scattering properties of the suspension. In a nematic phase, when the suspension was sandwiched with two glass plates, the film became opaque. This would be attributable to an appearance of both multidomain structures of LC alignment and mismatches of refractive indices between the materials. The opaque state turned into a transparent one when a nematic-to-isotropic phase transition was induced by the trans-to-cis photoisomerization of the azo-dye. This will result from a disappearance of both the multidomain structures and the refractive-index mismatches in the isotropic phase. The transparent film went back into the initial opaque film when the nematic phase was obtained by the cis-to-trans photoisomerization. In a LC emulsion in which glycerol or water droplets were dispersed in liquid crystals, we examined photochemical change of defect structures and inter-droplet distances by the photochemical manner. At the initial state, Saturn ring and hedgehog defects were formed around the droplets. For the glycerol droplets, we observed structural transformations between Saturn ring and boojums on irradiation with ultra-violet and visible light. For the water droplets, the inter-droplet distances varied by changing defect size on the irradiation. These phenomena would result from modulation of anchoring conditions of the droplets by the photoisomerization of the azo-dyes.

  13. 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.

  14. 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.

  15. In vitro interaction of colloidal nanoparticles with mammalian cells: What have we learned thus far?

    PubMed Central

    Nazarenus, Moritz; Zhang, Qian; Soliman, Mahmoud G; del Pino, Pablo; Pelaz, Beatriz; Carregal-Romero, Susana; Rejman, Joanna; Rothen-Rutishauser, Barbara; Clift, Martin J D; Zellner, Reinhard; Nienhaus, G Ulrich; Delehanty, James B; Medintz, Igor L

    2014-01-01

    Summary The interfacing of colloidal nanoparticles with mammalian cells is now well into its second decade. In this review our goal is to highlight the more generally accepted concepts that we have gleaned from nearly twenty years of research. While details of these complex interactions strongly depend, amongst others, upon the specific properties of the nanoparticles used, the cell type, and their environmental conditions, a number of fundamental principles exist, which are outlined in this review. PMID:25247131

  16. Transport of colloidal silica in unsaturated sand: Effect of charging properties of sand and silica particles.

    PubMed

    Fujita, Yosuke; Kobayashi, Motoyoshi

    2016-07-01

    We have studied the transport of colloidal silica in various degrees of a water-saturated Toyoura sand column, because silica particles are widely used as catalyst carriers and abrasive agents, and their toxicity is reported recently. Since water-silica, water-sand, and air-water interfaces have pH-dependent negative charges, the magnitude of surface charge was controlled by changing the solution pH. The results show that, at high pH conditions (pH 7.4), the deposition of colloidal silica to the sand surface is interrupted and the silica concentration at the column outlet immediately reaches the input concentration in saturated conditions. In addition, the relative concentration of silica at the column outlet only slightly decreases to 0.9 with decreasing degrees of water saturation to 38%, because silica particles are trapped in straining regions in the soil pore and air-water interface. On the other hand, at pH 5 conditions (low pH), where sand and colloid have less charge, reduced repulsive forces result in colloidal silica attaching onto the sand in saturated conditions. The deposition amount of silica particles remarkably increases with decreasing degrees of water saturation to 37%, which is explained by more particles being retained in the sand column associated with the air-water interface. In conclusion, at higher pH, the mobility of silica particles is high, and the air-water interface is inactive for the deposition of silica. On the other hand, at low pH, the deposition amount increases with decreasing water saturation, and the particle transport is inhibited.

  17. [The colloid milium: An observation associated with trichinosis].

    PubMed

    Okhremchuk, Ilona; Abed, Safia; Nguyen, Anh Tuan; Brandone, Nicolas; Morand, Jean-Jacques

    2016-04-01

    The colloid milium has four clinical forms: adult colloid milium, juvenile colloid milium, paracolloid (or nodular colloid degeneration) and pigmented colloid milium. We report the case of an adult colloid milium in a man of 56, who presented episodes of diffuse pruritus associated with myalgia and digestive disorders, indicative of trichinosis. He also developed gradually over the past 10 years, yellowish injuries in the mandibles and neck for whom histology objectified a colloid milium. Etiology and treatment are still unknown; association with a trichinosis is probably coincidental.

  18. Straining soft colloids in aqueous nematic liquid crystals

    NASA Astrophysics Data System (ADS)

    Mushenheim, Peter C.; Pendery, Joel S.; Weibel, Douglas B.; Spagnolie, Saverio E.; Abbott, Nicholas L.

    2016-05-01

    Liquid crystals (LCs), because of their long-range molecular ordering, are anisotropic, elastic fluids. Herein, we report that elastic stresses imparted by nematic LCs can dynamically shape soft colloids and tune their physical properties. Specifically, we use giant unilamellar vesicles (GUVs) as soft colloids and explore the interplay of mechanical strain when the GUVs are confined within aqueous chromonic LC phases. Accompanying thermal quenching from isotropic to LC phases, we observe the elasticity of the LC phases to transform initially spherical GUVs (diameters of 2-50 µm) into two distinct populations of GUVs with spindle-like shapes and aspect ratios as large as 10. Large GUVs are strained to a small extent (R/r < 1.54, where R and r are the major and minor radii, respectively), consistent with an LC elasticity-induced expansion of lipid membrane surface area of up to 3% and conservation of the internal GUV volume. Small GUVs, in contrast, form highly elongated spindles (1.54 < R/r < 10) that arise from an efflux of LCs from the GUVs during the shape transformation, consistent with LC-induced straining of the membrane leading to transient membrane pore formation. A thermodynamic analysis of both populations of GUVs reveals that the final shapes adopted by these soft colloids are dominated by a competition between the LC elasticity and an energy (˜0.01 mN/m) associated with the GUV-LC interface. Overall, these results provide insight into the coupling of strain in soft materials and suggest previously unidentified designs of LC-based responsive and reconfigurable materials.

  19. 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

  20. Diffusiophoretic Focusing of Suspended Colloids

    NASA Astrophysics Data System (ADS)

    Shi, Nan; Nery-Azevedo, Rodrigo; Abdel-Fattah, Amr I.; Squires, Todd M.

    2016-12-01

    Using a microfluidic system to impose and maintain controlled, steady-state multicomponent p H and electrolyte gradients, we present systems where the diffusiophoretic migration of suspended colloids leads them to focus at a particular position, even in steady-state gradients. We show that naively superpositing effects of each gradient may seem conceptually and qualitatively reasonable, yet is invalid due to the coupled transport of these multicomponent electrolytes. In fact, reformulating the classic theories in terms of the flux of each species (rather than local gradients) reveals rather stringent conditions that are necessary for diffusiophoretic focusing in steady gradients. Either particle surface properties must change as a function of local composition in solution (akin to isoelectric focusing in electrophoresis), or chemical reactions must occur between electrolyte species, for such focusing to be possible. The generality of these findings provides a conceptual picture for understanding, predicting, or designing diffusiophoretic systems.

  1. Oxyhydroxy Silicate Colloids: A New Type of Waterborne Actinide(IV) Colloids

    PubMed Central

    Weiss, Stephan; Hennig, Christoph; Brendler, Vinzenz; Ikeda‐Ohno, Atsushi

    2016-01-01

    Abstract At the near‐neutral and reducing aquatic conditions expected in undisturbed ore deposits or in closed nuclear waste repositories, the actinides Th, U, Np, and Pu are primarily tetravalent. These tetravalent actinides (AnIV) are sparingly soluble in aquatic systems and, hence, are often assumed to be immobile. However, AnIV could become mobile if they occur as colloids. This review focuses on a new type of AnIV colloids, oxyhydroxy silicate colloids. We herein discuss the chemical characteristics of these colloids and the potential implication for their environmental behavior. The binary oxyhydroxy silicate colloids of AnIV could be potentially more mobile as a waterborne species than the well‐known mono‐component oxyhydroxide colloids. PMID:27957406

  2. 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.

  3. Transport in charged colloids driven by thermoelectricity.

    PubMed

    Würger, Alois

    2008-09-05

    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.

  4. Linear colloidal crystal arrays by electrohydrodynamic printing

    NASA Astrophysics Data System (ADS)

    Poon, H. F.; Saville, D. A.; Aksay, I. A.

    2008-09-01

    We use electrohydrodynamic jets of colloidal suspensions to produce arrays of colloidal crystalline stripes on surfaces. A critical factor in maintaining a stable jet is the distance of separation between the nozzle and the surface. Colloidal crystalline stripes are produced as two wetting lines of the deployed suspension merge during drying. To ensure that the two wetting lines merge, the "deployed-line-width" to "particle size" ratio is kept below a critical value so that the capillary forces overcome the frictional forces between the particles and the substrate.

  5. Food colloids research: historical perspective and outlook.

    PubMed

    Dickinson, Eric

    2011-06-09

    Trends and past achievements in the field of food colloids are reviewed. Specific mention is made of advances in knowledge and understanding in the areas of (i) structure and rheology of protein gels, (ii) properties of adsorbed protein layers, (iii) functionality derived from protein-polysaccharide interactions, and (iv) oral processing of food colloids. Amongst ongoing experimental developments, the technique of particle tracking for monitoring local dynamics and microrheology of food colloids is highlighted. The future outlook offers exciting challenges with expected continued growth in research into digestion processes, encapsulation, controlled delivery, and nanoscience.

  6. Aggregation and Gelation of Anisometric Colloidal Particles

    NASA Astrophysics Data System (ADS)

    Mohraz, Ali; Solomon, Michael J.

    2002-11-01

    The quiescent and flow-induced structure and dynamics of colloidal aggregates and gels of anisometric particles are studied by means of static and dynamic light scattering. Ground-based studies of weak gels are possible due to the submicron size of the boehmite rod suspensions investigated; however, microgravity conditions would be required for more general studies. The properties of colloidal rod suspensions are compared to typical properties of spherical particle gels to understand the role of anisotropic excluded volume on gel structure and dynamics. The structure and dynamics of colloidal aggregates and gels have long been of scientific and technological interest; however, most research has focused on suspensions of spherical particles. Yet, aggregates and gels of anisometric particles - colloidal rods and platelets - may exhibit structure and dynamics that are quite different from spherical colloids. For example, suspensions of colloidal rods gel at extremely low volume fractions and form birefringent sediments. The rheology of solutions and gels of colloidal rods and platelets differs dramatically from that of colloidal spheres. Scientifically, studies with anisometric particles offer the opportunity to assess the role of anisotropic excluded volume and particle orientation in aggregates and gels. Technologically, anisometric colloids find use in a wide range of materials such as ceramics, polymer nanocomposites, well-bore drilling fluids and magnetic storage media. Model colloidal boehmite rods of approximately monodisperse dimension and aspect ratio have been synthesized according to the method of Philipse and coworkers. In aqueous solution, these materials undergo gelation upon the addition of divalent salt. By means of a novel grafting reaction and procedure for solvent refractive index matching, the rods have also been dispersed in mixed organic solvents. In this case, gelation is induced by means of depletion interaction. We report the effect of

  7. Study of colloids transport during two-phase flow using a novel polydimethylsiloxane micro-model.

    PubMed

    Zhang, Qiulan; Karadimitriou, N K; Hassanizadeh, S M; Kleingeld, P J; Imhof, A

    2013-07-01

    As a representation of a porous medium, a closed micro-fluidic device made of polydimethylsiloxane (PDMS), with uniform wettability and stable hydrophobic properties, was designed and fabricated. A flow network, with a mean pore size of 30 μm, was formed in a PDMS slab, covering an area of 1 mm × 10 mm. The PDMS slab was covered and bonded with a 120-μm-thick glass plate to seal the model. The glass plate was first spin-coated with a thin layer, roughly 10 μm, of PDMS. The micro-model was treated with silane in order to make it uniformly and stably hydrophobic. Fluorescent particles of 300 μm in diameter were used as colloids. It is known that more removal of colloids occurs under unsaturated conditions, compared to saturated flow in soil. At the same time, the change of saturation has been observed to cause remobilization of attached colloids. The mechanisms for these phenomena are not well understood. This is the first time that a closed micro-model, made of PDMS with uniform and stable wettability, has been used in combination with confocal microscopy to study colloid transport under transient two-phase flow conditions. With confocal microscopy, the movement of fluorescent particles and flow of two liquids within the pores can be studied. One can focus at different depths within the pores and thus determine where the particles exactly are. Thus, remobilization of attached colloids by moving fluid-fluid interfaces was visualized. In order to allow for the deposition and subsequent remobilization of colloids during two-phase flow, three micro-channels for the injection of liquids with and without colloids were constructed. An outlet channel was designed where effluent concentration breakthrough curves can be quantified by measuring the fluorescence intensity. A peak concentration also indicated in the breakthrough curve with the drainage event. The acquired images and breakthrough curve successfully confirmed the utility of the combination of such a PDMS

  8. 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.

  9. 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.

  10. 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.

  11. Transition from glass- to gel-like states in clay at a liquid interface

    PubMed Central

    Gholamipour-Shirazi, A.; Carvalho, M. S.; Huila, M. F. G.; Araki, K.; Dommersnes, P.; Fossum, J. O.

    2016-01-01

    Colloidal clay in water suspensions are known to exhibit a multitude of bulk phases depending on initial colloidal concentration and ionic strength, and examples of this include repulsive Wigner colloidal glasses at low ionic strength and attractive gels at higher ionic strength due to screened electrostatic forces by the electrolyte. From confocal Raman microscopy combined with elasticity measurements, we infer that clay trapped at quasi two-dimensional interfaces between oil and water also exhibit confined glass-like or gel-like states. The results can be important for the preparation of particles stabilized colloidal emulsions or colloidal capsules, and a better understanding of this phenomenon may lead to new emulsion or encapsulation technologies. PMID:27883031

  12. Transition from glass- to gel-like states in clay at a liquid interface

    NASA Astrophysics Data System (ADS)

    Gholamipour-Shirazi, A.; Carvalho, M. S.; Huila, M. F. G.; Araki, K.; Dommersnes, P.; Fossum, J. O.

    2016-11-01

    Colloidal clay in water suspensions are known to exhibit a multitude of bulk phases depending on initial colloidal concentration and ionic strength, and examples of this include repulsive Wigner colloidal glasses at low ionic strength and attractive gels at higher ionic strength due to screened electrostatic forces by the electrolyte. From confocal Raman microscopy combined with elasticity measurements, we infer that clay trapped at quasi two-dimensional interfaces between oil and water also exhibit confined glass-like or gel-like states. The results can be important for the preparation of particles stabilized colloidal emulsions or colloidal capsules, and a better understanding of this phenomenon may lead to new emulsion or encapsulation technologies.

  13. Charged colloids and polyelectrolytes: from statics to electrokinetics

    NASA Astrophysics Data System (ADS)

    Löwen, H.; Esztermann, A.; Wysocki, A.; Allahyarov, E.; Messina, R.; Jusufi, A.; Hoffmann, N.; Gottwald, D.; Kahl, G.; Konieczny, M.; Likos, C. N.

    2005-01-01

    A review is given on recent studies of charged colloidal suspensions and polyelectrolytes both in static and non-equilibrium situations. As far as static equilibrium situations are concerned, we discuss three different problems: 1) Sedimentation density profiles in charged suspensions are shown to exhibit a stretched non-bariometric wing at large heights and binary suspensions under gravity can exhibit an analog of the brazil-nut effect known from granular matter, i.e. the heavier particles settle on top of the lighter ones. 2) Soft polyelectrolyte systems like polyelectrolyte stars and microgels show an ultra-soft effective interaction and this results into an unusual equilibrium phase diagram including reentrant melting transitions and stable open crystalline lattices. 3) The freezing transition in bilayers of confined charged suspensions is discussed and a reentrant behaviour is obtained. As far as nonequilibrium problems are concerned, we discuss an interface instability in oppositely driven colloidal mixtures and discuss possible approaches to simulate electrokinetic effects in charged suspensions.

  14. Universal scaling of correlated diffusion in colloidal monolayers.

    PubMed

    Zhang, Wei; Li, Na; Bohinc, Klemen; Tong, Penger; Chen, Wei

    2013-10-18

    Using the techniques of optical microscopy and particle tracking, we measure the correlated diffusion in a monolayer of uniform silica spheres dispersed at a water-air interface. It is found that the correlated motion of the interfacial particles can be well described by two universal response functions, the normalized longitudinal and transverse diffusion coefficients D(∥)(r/r0) and D(⊥)(r/r0), where r is the interparticle distance and r0=a(λS/a)(3/2) is a new scaling length, which depends on both the Saffman length λS and particle radius a. The obtained response functions characterize the crossover behavior of the colloidal monolayers from the subphase-dominated three-dimensional hydrodynamics at low surface coverage to the monolayer-dominated 2D hydrodynamics at high concentrations. The surface viscosity ηs(2) of the colloidal monolayer obtained by two-particle rheology compares well with the one-particle measurements.

  15. Universal Scaling of Correlated Diffusion in Colloidal Monolayers

    NASA Astrophysics Data System (ADS)

    Zhang, Wei; Li, Na; Bohinc, Klemen; Tong, Penger; Chen, Wei

    2013-10-01

    Using the techniques of optical microscopy and particle tracking, we measure the correlated diffusion in a monolayer of uniform silica spheres dispersed at a water-air interface. It is found that the correlated motion of the interfacial particles can be well described by two universal response functions, the normalized longitudinal and transverse diffusion coefficients D˜∥(r/r0) and D˜⊥(r/r0), where r is the interparticle distance and r0=a(λS/a)3/2 is a new scaling length, which depends on both the Saffman length λS and particle radius a. The obtained response functions characterize the crossover behavior of the colloidal monolayers from the subphase-dominated three-dimensional hydrodynamics at low surface coverage to the monolayer-dominated 2D hydrodynamics at high concentrations. The surface viscosity ηs(2) of the colloidal monolayer obtained by two-particle rheology compares well with the one-particle measurements.

  16. Depinning transition and 2D superlubricity in incommensurate colloidal monolayers

    NASA Astrophysics Data System (ADS)

    Mandelli, Davide; Vanossi, Andrea; Manini, Nicola; Tosatti, Erio

    2014-03-01

    Colloidal monolayers sliding over periodic corrugated potential are highly tunable systems allowing to visualize the dynamics between crystalline surfaces. Based on molecular dynamics, Vanossi and coworkers reproduced the main experimental results and explored the potential impact of colloid sliding in nanotribology. The degree of interface commensurability was found to play a major role in determining the frictional properties, the static friction force Fs becoming vanishingly small in incommensurate geometries for weak corrugation U0.Lead by this result,here we systematically investigate the possibility to observe a 2D Aubry-like transition from a superlubric state to a pinned state for increasing U0. By using a reliable protocol, we generate annealed configurations at different values of U0 for an underdense monolayer. We find Fs to be vanishingly small up to a critical corrugation Uc coinciding with an abrupt structural transition in the ground state configuration. Similarly to what is observed in the Frenkel Kontorova model,this transition is characterized by a significant decrease in the number of particles sampling regions near the maxima of the substrate potential. Research partly sponsored by Sinergia Project CRSII2 136287-1 and ERC 2012ADG320796 MODPHYSFRICT.

  17. Quantum oscillations in magnetically doped colloidal nanocrystals.

    PubMed

    Ochsenbein, Stefan T; Gamelin, Daniel R

    2011-02-01

    Progress in the synthesis of colloidal quantum dots has recently provided access to entirely new forms of diluted magnetic semiconductors, some of which may find use in quantum computation. The usefulness of a spin qubit is defined by its Rabi frequency, which determines the operation time, and its coherence time, which sets the error correction window. However, the spin dynamics of magnetic impurity ions in colloidal doped quantum dots remain entirely unexplored. Here, we use pulsed electron paramagnetic resonance spectroscopy to demonstrate long spin coherence times of ∼0.9 µs in colloidal ZnO quantum dots containing the paramagnetic dopant Mn(2+), as well as Rabi oscillations with frequencies ranging between 2 and 20 MHz depending on microwave power. We also observe electron spin echo envelope modulations of the Mn(2+) signal due to hyperfine coupling with protons outside the quantum dots, a situation unique to the colloidal form of quantum dots, and not observed to date.

  18. Luminol chemiluminescence catalysed by colloidal platinum nanoparticles.

    PubMed

    Xu, Sheng-Liang; Cui, Hua

    2007-01-01

    Platinum colloids prepared by the reduction of hexachloroplatinic acid with citrate in the presence of different stabilizers were found to enhance the chemiluminescence (CL) of the luminol-H(2)O(2) system, and the most intensive CL signals were obtained with citrate-protected Pt colloids synthesized with citrate as both a reductant and a stabilizer. Light emission was intense and reproducible. Transmission electron microscopy and X-ray photoelectron spectroscopy studies were conducted before and after the CL reaction to investigate the possible CL enhancement mechanism. It is suggested that this CL enhancement is attributed to the catalysis of platinum nanoparticles, which could accelerate the electron-transfer process and facilitate the CL radical generation in aqueous solution. The effects of Pt colloids prepared by the hydroborate reduction were also investigated. The application of the luminol-H(2)O(2)-Pt colloids system was exploited for the determination of compounds such as uric acid, ascorbic acid, phenols and amino acids.

  19. Computer simulations of charged colloids in confinement.

    PubMed

    Puertas, Antonio M; de las Nieves, F Javier; Cuetos, Alejandro

    2015-02-15

    We study by computer simulations the interaction between two similarly charged colloidal particles confined between parallel planes, in salt free conditions. Both the colloids and ions are simulated explicitly, in a fine-mesh lattice, and the electrostatic interaction is calculated using Ewald summation in two dimensions. The internal energy is measured by setting the colloidal particles at a given position and equilibrating the ions, whereas the free energy is obtained introducing a bias (attractive) potential between the colloids. Our results show that upon confining the system, the internal energy decreases, resulting in an attractive contribution to the interaction potential for large charges and strong confinement. However, the loss of entropy of the ions is the dominant mechanism in the interaction, irrespective of the confinement of the system. The interaction potential is therefore repulsive in all cases, and is well described by the DLVO functional form, but effective values have to be used for the interaction strength and Debye length.

  20. 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)

  1. 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.

  2. Thin film interference of colloidal thin films.

    PubMed

    Cong, Hailin; Cao, Weixiao

    2004-09-14

    A stairlike colloidal crystal thin film composed of poly(styrene-methyl methacrylate-acrylic acid) (P(St-MMA-AA)) monodispersed colloids was fabricated on an inclined silicon substrate. Different bright colors were observed on the various parts of the film with different layers as white light irradiated perpendicularly on it. The relationship between the colors and layers of the film was investigated and discussed according to the principle of thin film interference. On the basis of the phenomenon of thin film interference, a one-layer colloidal film having uniform color was researched and it would display diverse colors before and after swollen by styrene (St). A circular stairlike colloidal film was achieved to mimic the colors of the peacock tail feather.

  3. Hemorrhagic Colloid Cyst Presenting with Acute Hydrocephaly

    PubMed Central

    Akhavan, Reza; Zandi, Behrouz; Pezeshki-Rad, Masoud; Farrokh, Donya

    2017-01-01

    Colloid cysts are benign slow-growing cystic lesions located on the roof of the third ventricle that usually present with symptoms related to gradual rise of intracranial pressure. They mostly remain asymptomatic and sometimes grow progressively and cause diverse symptoms associated with increased intracranial pressure such as headache, diplopia, and sixth cranial nerve palsy. Here we report a 47-year-old female who presented to the emergency department with acute severe headache and nausea/vomiting. On MRI examination acute hydrocephaly due to hemorrhagic colloid cyst was detected. Acute hemorrhage in colloid cysts is extremely rare and may present with symptoms of acute increase in the intracranial pressure. Intracystic hemorrhage is very rarely reported as a complication of colloid cyst presenting with paroxysmal symptoms of acute hydrocephaly. PMID:28210514

  4. 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

  5. Colloid milium: a rare cutaneous deposition disease.

    PubMed

    Rahman, Simeen Ber; Arfan Ul Bari; Mumtaz, Nadeem

    2008-04-01

    Colloid milium is a rare degenerative skin disorder known by the development of small translucent, yellowish brown pappular nodules or plaques, generally located in sun exposed areas. Clinically they are of two types, adult and juvenile type. We present a case of adult type Colloid milium in a 60 years old female patient with clinical and histological findings unmistakable of the condition. She was treated with IPL. (Intense Pulsed Light) laser following unsatisfactory response with dermabrasion.

  6. Compact Video Microscope Imaging System Implemented in Colloid Studies

    NASA Technical Reports Server (NTRS)

    McDowell, Mark

    2002-01-01

    Long description Photographs showing fiber-optic light source, microscope and charge-coupled discharge (CCD) camera head connected to camera body, CCD camera body feeding data to image acquisition board in PC, and Cartesian robot controlled via PC board. The Compact Microscope Imaging System (CMIS) is a diagnostic tool with intelligent controls for use in space, industrial, medical, and security applications. CMIS can be used in situ with a minimum amount of user intervention. This system can scan, find areas of interest in, focus on, and acquire images automatically. Many multiple-cell experiments require microscopy for in situ observations; this is feasible only with compact microscope systems. CMIS is a miniature machine vision system that combines intelligent image processing with remote control. The software also has a user-friendly interface, which can be used independently of the hardware for further post-experiment analysis. CMIS has been successfully developed in the SML Laboratory at the NASA Glenn Research Center and adapted for use for colloid studies and is available for telescience experiments. The main innovations this year are an improved interface, optimized algorithms, and the ability to control conventional full-sized microscopes in addition to compact microscopes. The CMIS software-hardware interface is being integrated into our SML Analysis package, which will be a robust general-purpose image-processing package that can handle over 100 space and industrial applications.

  7. Domain and droplet sizes in emulsions stabilized by colloidal particles

    NASA Astrophysics Data System (ADS)

    Frijters, Stefan; Günther, Florian; Harting, Jens

    2014-10-01

    Particle-stabilized emulsions are commonly used in various industrial applications. These emulsions can present in different forms, such as Pickering emulsions or bijels, which can be distinguished by their different topologies and rheology. We numerically investigate the effect of the volume fraction and the uniform wettability of the stabilizing spherical particles in mixtures of two fluids. For this, we use the well-established three-dimensional lattice Boltzmann method, extended to allow for the added colloidal particles with non-neutral wetting properties. We obtain data on the domain sizes in the emulsions by using both structure functions and the Hoshen-Kopelman (HK) algorithm, and we demonstrate that both methods have their own (dis)advantages. We confirm an inverse dependence between the concentration of particles and the average radius of the stabilized droplets. Furthermore, we demonstrate the effect of particles detaching from interfaces on the emulsion properties and domain-size measurements.

  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.

  9. 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.

  10. 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.

  11. 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.

  12. Colloids with high-definition surface structures.

    PubMed

    Chen, Hsien-Yeh; Rouillard, Jean-Marie; Gulari, Erdogan; Lahann, Joerg

    2007-07-03

    Compared with the well equipped arsenal of surface modification methods for flat surfaces, techniques that are applicable to curved, colloidal surfaces are still in their infancy. This technological gap exists because spin-coating techniques used in traditional photolithographic processes are not applicable to the curved surfaces of spherical objects. By replacing spin-coated photoresist with a vapor-deposited, photodefinable polymer coating, we have now fabricated microstructured colloids with a wide range of surface patterns, including asymmetric and chiral surface structures, that so far were typically reserved for flat substrates. This high-throughput method can yield surface-structured colloidal particles at a rate of approximately 10(7) to 10(8) particles per operator per day. Equipped with spatially defined binding pockets, microstructured colloids can engage in programmable interactions, which can lead to directed self-assembly. The ability to create a wide range of colloids with both simple and complex surface patterns may contribute to the genesis of previously unknown colloidal structures and may have important technological implications in a range of different applications, including photonic and phononic materials or chemical sensors.

  13. Colloids with high-definition surface structures

    PubMed Central

    Chen, Hsien-Yeh; Rouillard, Jean-Marie; Gulari, Erdogan; Lahann, Joerg

    2007-01-01

    Compared with the well equipped arsenal of surface modification methods for flat surfaces, techniques that are applicable to curved, colloidal surfaces are still in their infancy. This technological gap exists because spin-coating techniques used in traditional photolithographic processes are not applicable to the curved surfaces of spherical objects. By replacing spin-coated photoresist with a vapor-deposited, photodefinable polymer coating, we have now fabricated microstructured colloids with a wide range of surface patterns, including asymmetric and chiral surface structures, that so far were typically reserved for flat substrates. This high-throughput method can yield surface-structured colloidal particles at a rate of ≈107 to 108 particles per operator per day. Equipped with spatially defined binding pockets, microstructured colloids can engage in programmable interactions, which can lead to directed self-assembly. The ability to create a wide range of colloids with both simple and complex surface patterns may contribute to the genesis of previously unknown colloidal structures and may have important technological implications in a range of different applications, including photonic and phononic materials or chemical sensors. PMID:17592149

  14. Estuarine mixing behavior of colloidal organic carbon and colloidal mercury in Galveston Bay, Texas.

    PubMed

    Lee, Seyong; Han, Seunghee; Gill, Gary A

    2011-06-01

    Mercury (Hg) in estuarine water is distributed among different physical phases (i.e. particulate, colloidal, and truly dissolved). This phase speciation influences the fate and cycling of Hg in estuarine systems. However, limited information exists on the estuarine distribution of colloidal phase Hg, mainly due to the technical difficulties involved in measuring it. In the present study, we determined Hg and organic carbon levels from unfiltered, filtered (<0.45 μm), colloidal (10 kDa-0.45 μm), and truly dissolved (<10 kDa) fractions of Galveston Bay surface water in order to understand the estuarine mixing behavior of Hg species as well as interactions of Hg with colloidal organic matter. For the riverine end-member, the colloidal fraction comprised 43 ± 11% of the total dissolved Hg pool and decreased to 17 ± 8% in brackish water. In the estuarine mixing zone, dissolved Hg and colloidal organic carbon showed non-conservative removal behavior, particularly in the low salinity (<15 ppt) region. This removal may be caused by salt-induced coagulation of colloidal matter and consequent removal of dissolved Hg. The particle-water interaction, K(d) ([particulate Hg (mol kg(-1))]/[dissolved Hg (mol L(-1))]) of Hg decreased as particle concentration increased, while the particle-water partition coefficient based on colloidal Hg and the truly dissolved Hg fraction, K(c) ([colloidal Hg (mol kg(-1))]/[truly dissolved Hg (mol L(-1))]) of Hg remained constant as particle concentration increased. This suggests that the particle concentration effect is associated with the amount of colloidal Hg, increasing in proportion to the amount of suspended particulate matter. This work demonstrates that, colloidal organic matter plays an important role in the transport, particle-water partitioning, and removal of dissolved Hg in estuarine waters.

  15. Colloid's influences on microalgae growth as a potential environmental factor

    NASA Astrophysics Data System (ADS)

    Zhao, Xinhuai; Zhang, Zhengbin; Liu, Liansheng

    2003-09-01

    The role of colloid as “colloid pump” in the ocean is well known. The important influence of colloid in seawater on the growth of microalga was found in our 1999 2000 study. Colloid concentrates were obtained by employing a cross-flow filtration system to ultrafilter seawater (which had been pre-filtrated by 0.45 μm acetate cellulose membrane) successively with different membranes. Ultrafiltration retentions (we called them colloid concentrates) together with control sample (seawater without colloid) were then inoculated with two species of microalgae and cultivated in selected conditions. Monitoring of microalgae growth during cultivation showed that all colloid concentrates had obvious influence on the growth of the microalgae studied. Addition of Fe(OH)3 colloid or organic colloid (protein or carbohydrate) to the control sample enhanced the microalgae’s growth.

  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. Colloids and polymers in random colloidal matrices: Demixing under good-solvent conditions

    NASA Astrophysics Data System (ADS)

    Annunziata, Mario Alberto; Pelissetto, Andrea

    2012-10-01

    We consider a simplified coarse-grained model for colloid-polymer mixtures, in which polymers are represented as monoatomic molecules interacting by means of pair potentials. We use it to study polymer-colloid segregation in the presence of a quenched matrix of colloidal hard spheres. We fix the polymer-to-colloid size ratio to 0.8 and consider matrices such that the fraction f of the volume that is not accessible to the colloids due to the matrix is equal to 40%. As in the Asakura-Oosawa-Vrij (AOV) case, we find that binodal curves in the polymer and colloid volume-fraction plane have a small dependence on disorder. As for the position of the critical point, the behavior differs from that observed in the AOV case: While the critical colloid volume fraction is essentially the same in the bulk and in the presence of the matrix, the polymer volume fraction at criticality increases as f increases. At variance with the AOV case, no capillary colloid condensation or evaporation is generically observed.

  18. Colloids and polymers in random colloidal matrices: demixing under good-solvent conditions.

    PubMed

    Annunziata, Mario Alberto; Pelissetto, Andrea

    2012-10-01

    We consider a simplified coarse-grained model for colloid-polymer mixtures, in which polymers are represented as monoatomic molecules interacting by means of pair potentials. We use it to study polymer-colloid segregation in the presence of a quenched matrix of colloidal hard spheres. We fix the polymer-to-colloid size ratio to 0.8 and consider matrices such that the fraction f of the volume that is not accessible to the colloids due to the matrix is equal to 40%. As in the Asakura-Oosawa-Vrij (AOV) case, we find that binodal curves in the polymer and colloid volume-fraction plane have a small dependence on disorder. As for the position of the critical point, the behavior differs from that observed in the AOV case: While the critical colloid volume fraction is essentially the same in the bulk and in the presence of the matrix, the polymer volume fraction at criticality increases as f increases. At variance with the AOV case, no capillary colloid condensation or evaporation is generically observed.

  19. 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.

  20. Stabilization of plutonium nano-colloids by epitaxial distortion on mineral surfaces.

    PubMed

    Powell, Brian A; Dai, Zurong; Zavarin, Mavrik; Zhao, Pihong; Kersting, Annie B

    2011-04-01

    The subsurface migration of Pu may be enhanced by the presence of colloidal forms of Pu. Therefore, complete evaluation of the risk posed by subsurface Pu contamination needs to include a detailed physical/chemical understanding of Pu colloid formation and interactions of Pu colloids with environmentally relevant solid phases. Transmission electron microscopy (TEM) was used to characterize Pu nanocolloids and interactions of Pu nanocolloids with goethite and quartz. We report that intrinsic Pu nanocolloids generated in the absence of goethite or quartz were 2-5 nm in diameter, and both electron diffraction analysis and HRTEM confirm the expected Fm3m space group with the fcc, PuO2 structure. Plutonium nanocolloids formed on goethite have undergone a lattice distortion relative to the ideal fluorite-type structure, fcc, PuO2, resulting in the formation of a bcc, Pu4O7 structure. This structural distortion results from an epitaxial growth of the plutonium colloid on goethite, leading to stronger binding of plutonium to goethite compared with other minerals such as quartz, where the distortion was not observed. This finding provides new insight for understanding how molecular-scale behavior at the mineral-water interface may facilitate transport of plutonium at the field scale.

  1. Assembling nanoparticle coatings to improve the drug delivery performance of lipid based colloids

    NASA Astrophysics Data System (ADS)

    Simovic, Spomenka; Barnes, Timothy J.; Tan, Angel; Prestidge, Clive A.

    2012-02-01

    Lipid based colloids (e.g. emulsions and liposomes) are widely used as drug delivery systems, but often suffer from physical instabilities and non-ideal drug encapsulation and delivery performance. We review the application of engineered nanoparticle layers at the interface of lipid colloids to improve their performance as drug delivery systems. In addition we focus on the creation of novel hybrid nanomaterials from nanoparticle-lipid colloid assemblies and their drug delivery applications. Specifically, nanoparticle layers can be engineered to enhance the physical stability of submicron lipid emulsions and liposomes, satbilise encapsulated active ingredients against chemical degradation, control molecular transport and improve the dermal and oral delivery characteristics, i.e. increase absorption, bioavailability and facilitate targeted delivery. It is feasible that hybrid nanomaterials composed of nanoparticles and colloidal lipids are effective encapsulation and delivery systems for both poorly soluble drugs and biological drugs and may form the basis for the next generation of medicines. Additional pre-clinical research including specific animal model studies are required to advance the peptide/protein delivery systems, whereas the silica lipid hybrid systems have now entered human clinical trials for poorly soluble drugs.

  2. Direct numerical simulations of agglomeration of circular colloidal particles in two-dimensional shear flow

    SciTech Connect

    Choi, Young Joon Djilali, Ned

    2016-01-15

    Colloidal agglomeration of nanoparticles in shear flow is investigated by solving the fluid-particle and particle-particle interactions in a 2D system. We use an extended finite element method in which the dynamics of the particles is solved in a fully coupled manner with the flow, allowing an accurate description of the fluid-particle interfaces without the need of boundary-fitted meshes or of empirical correlations to account for the hydrodynamic interactions between the particles. Adaptive local mesh refinement using a grid deformation method is incorporated with the fluid-structure interaction algorithm, and the particle-particle interaction at the microscopic level is modeled using the Lennard-Jones potential. Motivated by the process used in fabricating fuel cell catalysts from a colloidal ink, the model is applied to investigate agglomeration of colloidal particles under external shear flow in a sliding bi-periodic Lees-Edwards frame with varying shear rates and particle fraction ratios. Both external shear and particle fraction are found to have a crucial impact on the structure formation of colloidal particles in a suspension. Segregation intensity and graph theory are used to analyze the underlying agglomeration patterns and structures, and three agglomeration regimes are identified.

  3. Ultrastructural changes in hepatic sinusoidal endothelial cells acutely exposed to colloidal iron.

    PubMed

    Bassett, Mark L; Dahlstrom, Jane E; Taylor, Matthew C; Koina, Mark E; Maxwell, Lesley; Francis, Douglas; Jain, Sanjiv; McLean, Allan J

    2003-07-01

    Hepatic sinusoidal endothelial cells form an important interface between the vascular system, represented by the sinusoids, and the space of Disse that surrounds the hepatocyte microvilli. This study aimed to assess the light microscopic and ultrastructural effects of acute exposure of hepatic sinusoidal endothelial cells to colloidal iron by injection of rats with iron polymaltose. Eight minutes after a single intravenous injection of iron polymaltose sinusoidal endothelial cells showed defenestration, and thickening and layering as assessed by transmission electron microscopy. Kupffer cells and stellate cells appeared activated. These changes were not observed in control animals, experiments using equivalent doses of maltose, or experiments using colloidal carbon except for Kupffer cell activation due to colloidal carbon. No significant light microscopic changes were seen in study or control animals. The findings indicate that acute exposure to colloidal iron causes changes in hepatic sinusoidal endothelial cells, stellate cells and Kupffer cells. This may be the result of a direct toxic effect of iron or increased production of reactive oxygen species. These observations suggest a possible mechanism for defenestration of sinusoidal endothelial cells in ageing and in disease states.

  4. 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.

  5. Drying of thin colloidal films

    NASA Astrophysics Data System (ADS)

    Routh, Alexander F.

    2013-04-01

    When thin films of colloidal fluids are dried, a range of transitions are observed and the final film profile is found to depend on the processes that occur during the drying step. This article describes the drying process, initially concentrating on the various transitions. Particles are seen to initially consolidate at the edge of a drying droplet, the so-called coffee-ring effect. Flow is seen to be from the centre of the drop towards the edge and a front of close-packed particles passes horizontally across the film. Just behind the particle front the now solid film often displays cracks and finally the film is observed to de-wet. These various transitions are explained, with particular reference to the capillary pressure which forms in the solidified region of the film. The reasons for cracking in thin films is explored as well as various methods to minimize its effect. Methods to obtain stratified coatings through a single application are considered for a one-dimensional drying problem and this is then extended to two-dimensional films. Different evaporative models are described, including the physical reason for enhanced evaporation at the edge of droplets. The various scenarios when evaporation is found to be uniform across a drying film are then explained. Finally different experimental techniques for examining the drying step are mentioned and the article ends with suggested areas that warrant further study.

  6. Self-assembly of gold nanoparticles and polystyrene: a highly versatile approach to the preparation of colloidal particles with polystyrene cores and gold nanoparticle coronae.

    PubMed

    Tian, Jia; Jin, Jie; Zheng, Fan; Zhao, Hanying

    2010-06-01

    Colloidal particles with polystyrene (PS) cores and gold nanoparticle (AuNP) coronae were prepared on the basis of the self-assembly of AuNP's and PS. Citrate-stabilized AuNP's were dispersed in aqueous solution, and PS with thiol terminal groups (PS-SH) was dissolved in toluene. A stable emulsion was obtained by mixing the two solutions. Optical microscope images indicate that after grafting of PS-SH to the citrate-stabilized AuNP's at liquid-liquid interface, the interfacial tension is reduced and the average size of toluene droplets in the emulsion decreases. Transmission electron microscope (TEM) results also prove the grafting of PS-SH to AuNP's and the location of the hybrid nanoparticles at the liquid-liquid interface. Colloidal particles with PS cores and AuNP coronae were prepared by adding the emulsion to excess methanol. The weight ratio of PS-SH to AuNP exerts a significant effect on the size of colloidal particles. TEM and dynamic light scattering results both indicate that the size of colloidal particles increases with the weight ratio. The application of the core-shell-structured colloidal particles to protein separation was also investigated in this research. Colloidal particles with PS-coated magnetic nanoparticles in the cores were also prepared by this strategy.

  7. Self-Pinning by Colloids Confined at a Contact Line

    NASA Astrophysics Data System (ADS)

    Weon, Byung Mook; Je, Jung Ho

    2013-01-01

    Colloidal particles suspended in a fluid usually inhibit complete wetting of the fluid on a solid surface and cause pinning of the contact line, known as self-pinning. We show differences in spreading and drying behaviors of pure and colloidal droplets using optical and confocal imaging methods. These differences come from spreading inhibition by colloids confined at a contact line. We propose a self-pinning mechanism based on spreading inhibition by colloids. We find a good agreement between the mechanism and the experimental result taken by directly tracking individual colloids near the contact lines of evaporating colloidal droplets.

  8. 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.

  9. Capillary migration of microdisks on curved interfaces.

    PubMed

    Yao, Lu; Sharifi-Mood, Nima; Liu, Iris B; Stebe, Kathleen J

    2015-07-01

    The capillary energy landscape for particles on curved fluid interfaces is strongly influenced by the particle wetting conditions. Contact line pinning has now been widely reported for colloidal particles, but its implications in capillary interactions have not been addressed. Here, we present experiment and analysis for disks with pinned contact lines on curved fluid interfaces. In experiment, we study microdisk migration on a host interface with zero mean curvature; the microdisks have contact lines pinned at their sharp edges and are sufficiently small that gravitational effects are negligible. The disks migrate away from planar regions toward regions of steep curvature with capillary energies inferred from the dissipation along particle trajectories which are linear in the deviatoric curvature. We derive the curvature capillary energy for an interface with arbitrary curvature, and discuss each contribution to the expression. By adsorbing to a curved interface, a particle eliminates a patch of fluid interface and perturbs the surrounding interface shape. Analysis predicts that perfectly smooth, circular disks do not migrate, and that nanometric deviations from a planar circular, contact line, like those around a weakly roughened planar disk, will drive migration with linear dependence on deviatoric curvature, in agreement with experiment.

  10. Photophysical Properties of Colloidal Mn(II)-Doped CdSe Nanoparticles: Exchange Fields, Exciton Storage, and Light-Induced Spontaneous Magnetization

    NASA Astrophysics Data System (ADS)

    Beaulac, Remi

    2010-03-01

    An attractive approach to controlling spin effects in semiconductor nanostructures for applications in electronics is to use light to generate, manipulate, or read out spins. The main focus of this presentation will be on the recent demonstration of spontaneous photoinduced polarization of Mn(II) spins in doped colloidal CdSe quantum dots, an effect due to the formation of excitonic magnetic polarons. Photoexcitation generates large dopant-carrier exchange fields, enhanced by strong spatial confinement, that lead to giant Zeeman splittings of the semiconductor band structure in the absence of applied magnetic fields. These internal exchange fields allow spontaneous magnetic saturation of the Mn(II) spins to be achieved at zero external magnetic field up to ca. 50 K, and photomagnetic effects are observed all the way up to room temperature. The factors that allow this fascinating effect to be observed in colloidal Mn(II)-doped CdSe nanoparticles will be discussed. Relevant Publications: 1) Beaulac, Schneider, Archer, Bacher, and Gamelin. Science, 325, 973 (2009) 2) Beaulac, Archer, Ochsenbein, and Gamelin, Adv. Funct. Mat., 18, 3873 (2008)

  11. Ceramic Interfaces

    SciTech Connect

    Yet-Ming Chiang

    2004-10-28

    During the period of this grant, we significantly advanced the understanding of stable surface amorphous films (SAFs), the existence of which was first postulated and then demonstrated under this program. SAFs are nanometer-thick amorphous films which are characterized by a self-selecting thickness, and a composition and structure distinct from the bulk phases with which they coexist. Importantly, they are present as an equilibrium, disordered phase below bulk solidus temperatures where all other phases in the system are crystalline. They are true surface phases which coexist in thermodynamic equilibrium with the bulk phases. We have shown that SAFs form in a number of binary oxide systems, and that they play an important role in the processing of materials (e.g., solid-state activated sintering in ZnO-Bi2O3) and in forming surface-active layers in supported catalyst systems. These experimental results as well as a theoretical model for the stability of SAFs have now been published. We believe that SAFs can be controlled and manipulated in a wide range of systems, with potential applications in nanotechnology, MEMS, microelectronics, adhesion, and colloidal crystals.

  12. Single crystal growth and anisotropic crystal-fluid interfacial free energy in soft colloidal systems.

    PubMed

    Nguyen, Van Duc; Hu, Zhibing; Schall, Peter

    2011-07-01

    We measure the anisotropy of the crystal-fluid interfacial free energy in soft colloidal systems. A temperature gradient is used to direct crystal nucleation and control the growth of large single crystals in order to achieve well-equilibrated crystal-fluid interfaces. Confocal microscopy is used to follow both the growth process and the equilibrium crystal-fluid interface at the particle scale: heterogeneous crystal nucleation, the advancing interface, and the stationary equilibrium interface. We use the measured growth velocity to determine the chemical potential difference between crystal and fluid phases. Well-equilibrated, large crystal-fluid interfaces are then used to determine the interfacial free energy and its anisotropy directly from thermally excited interface fluctuations. We find that while the measured average interfacial free energy is in good agreement with values found in simulations, the anisotropy is significantly larger than simulation values. Finally, we investigate the effect of impurities on the advancing interface. We determine the critical force needed to overcome impurity particles from the local interface curvature.

  13. Rheological properties of Cubic colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Boromand, Arman; Maia, Joao

    2016-11-01

    Colloidal and non-colloidal suspensions are ubiquitous in many industrial application. There are numerous studies on these systems to understand and relate their complex rheological properties to their microstructural evolution under deformation. Although most of the experimental and simulation studies are centered on spherical particles, in most of the industrial applications the geometry of the colloidal particles deviate from the simple hard sphere and more complex geometries exist. Recent advances in microfabrication paved the way to fabricate colloidal particles with complex geometries for applications in different areas such as drug delivery where the fundamental understanding of their dynamics has remained unexplored. In this study, using dissipative particle dynamics, we investigate the rheological properties of cubic (superball) particles which are modeled as the cluster of core-modified DPD particles. Explicit representation of solvent particles in the DPD scheme will conserve the full hydrodynamic interactions between colloidal particles. Rheological properties of these cubic suspensions are investigated in the dilute and semi-dilute regimes. The Einstein and Huggins coefficients for these particles with different superball exponent will be calculate which represent the effect of single particle's geometry and multibody interactions on viscosity, respectively. The response of these suspensions is investigated under simple shear and oscillatory shear where it is shown that under oscillation these particles tend to form crystalline structure giving rise to stronger shear-thinning behavior recently measured experimentally.

  14. Quasicrystalline tilings with nematic colloidal platelets

    PubMed Central

    Dontabhaktuni, Jayasri; Ravnik, Miha; Žumer, Slobodan

    2014-01-01

    Complex nematic fluids have the remarkable capability for self-assembling regular colloidal structures of various symmetries and dimensionality according to their micromolecular orientational order. Colloidal chains, clusters, and crystals were demonstrated recently, exhibiting soft-matter functionalities of robust binding, spontaneous chiral symmetry breaking, entanglement, shape-driven and topological driven assembly, and even memory imprinting. However, no quasicrystalline structures were found. Here, we show with numerical modeling that quasicrystalline colloidal lattices can be achieved in the form of original Penrose P1 tiling by using pentagonal colloidal platelets in layers of nematic liquid crystals. The tilings are energetically stabilized with binding energies up to 2500 kBT for micrometer-sized platelets and further allow for hierarchical substitution tiling, i.e., hierarchical pentagulation. Quasicrystalline structures are constructed bottom-up by assembling the boat, rhombus, and star maximum density clusters, thus avoiding other (nonquasicrystalline) stable or metastable configurations of platelets. Central to our design of the quasicrystalline tilings is the symmetry breaking imposed by the platelet shape and the surface anchoring conditions at the colloidal platelets, which are misaligning and asymmetric over two perpendicular mirror planes. Finally, the design of the quasicrystalline tilings as platelets in nematic liquid crystals is inherently capable of a continuous variety of length scales of the tiling, ranging over three orders of magnitude in the typical length (from to ), which could allow for the design of quasicrystalline photonics at multiple frequency ranges. PMID:24550269

  15. Colloids with continuously tunable surface charge.

    PubMed

    van Ravensteijn, Bas G P; Kegel, Willem K

    2014-09-09

    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.

  16. 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.

  17. 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.

  18. 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.

  19. Design, synthesis, and film formation of stimuli-responsive colloidal dispersions containing phospholipids

    NASA Astrophysics Data System (ADS)

    Lestage, David Jackson

    These studies were undertaken to further understand the design of colloidal dispersions containing bio-active phospholipids (PL) as stabilizing agents and their stimuli-responsive behaviors during film formation. Methyl methacrylate (MMA) and n-butyl acrylate (nBA) dispersions were synthesized using anionic surfactants and PL, and the surface-responsiveness of coalesced films was monitored at the film-air (F-A) and film-substrate (F-S) interfaces after exposure to temperature, UV, pH, ionic strength, and enzymatic stimuli. Using spectroscopic molecular-level probes such as attenuated total reflectance (ATR) and internal reflection IR imaging (IRIRI), these studies show that structural features of PL and surfactants significantly affect stimuli-responsiveness of polymeric films. MMA/nBA homopolymer, blend, copolymer, and core-shell particle coalescence studies indicated that controlled permeability is influenced by particle composition and sodium dioctyl sulfosuccinate (SDOSS) mobility to the F-A interface is enhanced in response to temperature. Utilization of hydrogenated soybean phosphocholine (HSPC) as a co-surfactant with SDOSS resulted in bimodal p-MMA/nBA colloidal particles, and experiments showed that ionic interactions with HSPC inhibit SDOSS mobility. However, the controlled release of individual species is detected in the presence of Ca2+ ionic strength stimuli. Utilizing 1,2-bis(10,12-tricosadiynoyl)- sn-glycero-3-phosphocholine (DCPC), cocklebur-shape particle morphologies were obtained and using transmission electron microscopy (TEM), self-assembled tubules were detected at particle interfaces, but not in the presence of Ca 2+. At altered concentration levels of DCPC, surface localized ionic clusters (SLICs) composed of SDOSS and DCPC form at the F-A and F-S interfaces in response to temperature and ionic strength stimuli. Micelle formation of 1-myristoyl-2-hydroxy-sn-glycero-phosphocholine (MHPC) stabilizes unimodal p-MMA/nBA colloidal particles

  20. 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.

  1. Colloidal crystallization of colloidal silica modified with ferrocenyl group-contained polymers in organic solvents.

    PubMed

    Yoshinaga, Kohji; Shigeta, Maki; Komune, Seishu; Mouri, Emiko; Nakai, Akemi

    2007-01-15

    Surface modification of colloidal silica with ferrocenyl-grafted polymer and colloidal crystallization of the particles in organic solvent were studied. Poly(methyl methacrylate-co-vinylferrocene)-grafted silica never formed colloidal crystals in polar solvent, such as acetone, acetonitrile, ethanol and N,N-dimethylformamide (DMF), while poly(methyl methacrylate-co-ferrocenyl acrylate)-grafted silica gave colloidal crystallization in DMF. The particles prepared by grafting of poly(N,N-dimethylacrylamide-co-vinylferrocene), with vinylferrocene (Vfc) mole fraction of 1/13 and 1/23, were observed to give the crystallization in ethanol and DMF over particle volume fraction of 0.058. Further, silica modified with copolymer of Vfc and N-vinyl-2-pyrrolidone, N-vinylcarbazole or N-isopropylacrylamide formed colloidal crystals in ethanol and DMF. Especially, poly(N-isopropylacrylamide-co-Vfc)-grafted silica, which was composed of the highest mole fraction of vinylferrocene, 1/3, afforded colloidal crystallization in ethanol over particle volume fraction of 0.053. Relatively high polar vinylferrocene copolymer grafting of silica resulted in colloidal polymerization in organic solvents.

  2. Electrochemical reduction of chlorophyll in colloidal solutions

    SciTech Connect

    Suponeva, E.P.; Kadoshnikova, I.G.; Kazakova, A.A.; Kiselev, B.A.

    1986-02-01

    This paper discusses determining the energy yield of the photochemical reaction. The authors investigated the peculiarities of the electrochemical reduction of Chl in the colloidal state, where the elements of the molecular organization of the pigments in the reaction centers of photosynthesis are simulated and, as a result, the lifetime of Chl.- is substantially increased. Polarograms of a colloidal solution of Chl ''a'' in aqueous buffer solution contining less than 5% acetone are presented. The adsorption spectra were measured on a spectrophotometer and the fluorescence spectra were recorded on a setup assembled on the basis of RM-w and FEU-30 monochromators. The results obtained are evidence of the ability of Chl for spontaneous formation of molecular associates in aqueous medium, which are characterized by hindrance of the protonation of Chl.- in comparison with monomeric Chl at a high rate of exchange of an electron between the eletrode and the colloidal particle and between molecules in the volume of the particle.

  3. Spin Dynamics of Charged Colloidal Quantum Dots

    NASA Astrophysics Data System (ADS)

    Stern, N. P.

    2005-03-01

    Colloidal semiconductor quantum dots are promising structures for controlling spin phenomena because of their highly size- tunable physical properties, ease of manufacture, and nanosecond-scale spin lifetimes at room temperature. Recent experiments have succeeded in controlling the charging of the lowest electronic state of colloidal quantum dots ootnotetextC. Wang, B. L. Wehrenberg, C. Y. Woo, and P. Guyot-Sionnest, J. Phys. Chem B 108, 9027 (2004).. Here we use time-resolved Faraday rotation measurements in the Voigt geometry to investigate the spin dynamics of colloidal CdSe quantum dot films in both a charged and uncharged state at room temperature. The charging of the film is controlled by applying a voltage in an electrochemical cell and is confirmed by absorbance measurements. Significant changes in the spin precession are observed upon charging, reflecting the voltage- controlled electron occupation of the quantum dot states and filling of surface states.

  4. Targeted delivery of colloids by swimming bacteria

    NASA Astrophysics Data System (ADS)

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

    2013-10-01

    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.

  5. 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.

  6. 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

  7. Manipulating colloidal assemblies with active dopants

    NASA Astrophysics Data System (ADS)

    Ramananarivo, Sophie; Palacci, Jeremie

    2016-11-01

    The dynamics of a densely packed 2D layer of colloids can be significantly altered upon introducing a small amount of active microparticles. Those motile intruders drive the system out-of-equilibrium, which produces a variety of new complex phenomena such as the accentuation of density heterogeneities or the reorganization of crystalline colloidal structures. We investigate the altered dynamics of the passive spheres, as well as the behavior of micro-swimmers propelling in such crowded environment where interactions with passive obstacles or other active units become important. Ultimately, understanding and controlling such mixed systems could open new routes toward activity-assisted manipulation of colloids, potentially guiding the design of materials able to self-anneal their defects.

  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. Plasmonic films based on colloidal lithography.

    PubMed

    Ai, Bin; Yu, Ye; Möhwald, Helmuth; Zhang, Gang; Yang, Bai

    2014-04-01

    This paper reviews recent advances in the field of plasmonic films fabricated by colloidal lithography. Compared with conventional lithography techniques such as electron beam lithography and focused ion beam lithography, the unconventional colloidal lithography technique with advantages of low-cost and high-throughput has made the fabrication process more efficient, and moreover brought out novel films that show remarkable surface plasmon features. These plasmonic films include those with nanohole arrays, nanovoid arrays and nanoshell arrays with precisely controlled shapes, sizes, and spacing. Based on these novel nanostructures, optical and sensing performances can be greatly enhanced. The introduction of colloidal lithography provides not only efficient fabrication processes but also plasmonic films with unique nanostructures, which are difficult to be fabricated by conventional lithography techniques.

  10. Dynamic Assembly of Magnetic Colloidal Vortices

    SciTech Connect

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

    2016-04-29

    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.

  11. Energy transport velocity in bidispersed magnetic colloids

    NASA Astrophysics Data System (ADS)

    Bhatt, Hem; Patel, Rajesh; Mehta, R. V.

    2012-07-01

    Study of energy transport velocity of light is an effective background for slow, fast, and diffuse light and exhibits the photonic property of the material. We report a theoretical analysis of magnetic field dependent resonant behavior in forward-backward anisotropy factor, light diffusion constant, and energy transport velocity for bidispersed magnetic colloids. A bidispersed magnetic colloid is composed of micrometer size magnetic spheres dispersed in a magnetic nanofluid consisting of magnetic nanoparticles in a nonmagnetic liquid carrier. Magnetic Mie resonances and reduction in energy transport velocity accounts for the possible delay (longer dwell time) by field dependent resonant light transport. This resonant behavior of light in bidispersed magnetic colloids suggests a novel magnetophotonic material.

  12. 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.

  13. A fast algorithm for treating dielectric discontinuities in charged spherical colloids.

    PubMed

    Xu, Zhenli

    2012-03-01

    Electrostatic interactions between multiple colloids in ionic fluids are attracting much attention in studies of biological and soft matter systems. The evaluation of the polarization surface charges due to the spherical dielectric discontinuities poses a challenging problem to highly efficient computer simulations. In this paper, we propose a new method for fast calculating the electric field of spaced spheres using the multiple reflection expansion. The method uses a technique of recursive reflections among the spherical interfaces based on a formula of the multiple image representation, resulting in a simple, accurate and close-form expression of the surface polarization charges. Numerical calculations of the electric potential energies of charged spheres demonstrate the method is highly accurate with small number of reflections, and thus attractive for the use in practical simulations of related problems such as colloid suspension and macromolecular interactions.

  14. Colloid and materials science for the conservation of cultural heritage: cleaning, consolidation, and deacidification.

    PubMed

    Baglioni, Piero; Chelazzi, David; Giorgi, Rodorico; Poggi, Giovanna

    2013-04-30

    Serendipity and experiment have been a frequent approach for the development of materials and methodologies used for a long time for either cleaning or consolidation of works of art. Recently, new perspectives have been opened by the application of materials science, colloid science, and interface science frameworks to conservation, generating a breakthrough in the development of innovative tools for the conservation and preservation of cultural heritage. This Article is an overview of the most recent contributions of colloid and materials science to the art conservation field, mainly focusing on the use of amphiphile-based fluids, gels, and alkaline earth metal hydroxide nanoparticles dispersions for the cleaning of pictorial surfaces, the consolidation of artistic substrates, and the deacidification of paper, canvas, and wood. Future possible directions for solving several conservation issues that still need to be faced are also highlighted.

  15. Predicting the phase diagram of two-dimensional colloidal systems with long-range interactions.

    PubMed

    Mejía-Rosales, Sergio J; Gil-Villegas, Alejandro; Ivlev, Boris I; Ruiz-García, Jaime

    2006-11-09

    The phase diagram of a two-dimensional model system for colloidal particles at the air-water interface was determined using Monte Carlo computer simulations in the isothermic-isobaric ensemble. The micrometer-range binary colloidal interaction has been modeled by hard disklike particles interacting via a secondary minimum followed by a weaker longer-range repulsive maximum, both of the order of kBT. The repulsive part of the potential drives the clustering of particles at low densities and low temperatures. Pinned voids are formed at higher densities and intermediate values of the surface pressure. The analysis of isotherms, translational and orientational correlation functions as well as structure factor gives clear evidence of the presence of a melting first-order transition. However, the melting process can be also followed by a metastable route through a hexatic phase at low surface pressures and low temperatures, before crystalization occurs at higher surface pressure.

  16. Roles of Colloidal Silicon Dioxide Particles in Chemical Mechanical Polishing of Dielectric Silicon Dioxide

    NASA Astrophysics Data System (ADS)

    Choi, Wonseop; Singh, Rajiv K.

    2005-12-01

    Chemical mechanical polishing (CMP) is carried out using slurry particles in contact with a wafer and a pad. The size and distribution of particles between the wafer and the pad play a crucial role in achieving desired CMP performance. Polishing rates and friction forces were measured as a function of particle size and solids loading, and surface finishes of silica wafers polished with colloidal silica particles were analyzed to validate the polishing mechanism. On the basis of polishing rate, friction force and surface finish, polishing occurring at the pad-particles-wafer interface was analyzed and an interfacial contact model was proposed. Understanding the polishing mechanism using colloidal particles makes it possible to achieve desired CMP performance.

  17. 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.

  18. Highly Elastic and Self-Healing Composite Colloidal Gels.

    PubMed

    Diba, Mani; Wang, Huanan; Kodger, Thomas E; Parsa, Shima; Leeuwenburgh, Sander C G

    2017-03-01

    Composite colloidal gels are formed by the pH-induced electrostatic assembly of silica and gelatin nanoparticles. These injectable and moldable colloidal gels are able to withstand substantial compressive and tensile loads, and exhibit a remarkable self-healing efficiency. This study provides new, critical insight into the structural and mechanical properties of composite colloidal gels and opens up new avenues for practical application of colloidal gels.

  19. Colloid straining within saturated heterogeneous porous media.

    PubMed

    Porubcan, Alexis A; Xu, Shangping

    2011-02-01

    The transport of 0.46 μm, 2.94 μm, 5.1 μm and 6.06 μm latex particles in heterogeneous porous media prepared from the mixing of 0.78 mm, 0.46 mm and 0.23 mm quartz sands was investigated through column transport experiments. It was observed that the 0.46 μm particles traveled conservatively within the heterogeneous porous media, suggesting that under the experimental conditions employed in this research the strong repulsive interactions between the negatively charged latex particles and the clean quartz sands led to minimal colloid immobilization due to physicochemical filtration. The immobilization of the 2.94 μm, 5.1 μm and 6.06 μm latex particles was thus attributed to colloid straining. Experimental results showed that the straining of colloidal particles within heterogeneous sand mixtures increased when the fraction of finer sands increased. The mathematical model that was developed and tested based on results obtained using uniform sands (Xu et al., 2006) was found to be able to describe colloid straining within heterogeneous porous media. Examination of the relationship between the best-fit values of the clean-bed straining rate coefficients (k(0)) and the ratio of colloid diameter (d(p)) and sand grain size (d(g)) indicated that when number-average sizes were used to represent the size of the heterogeneous porous media, there existed a consistent relationship for both uniform sands and heterogeneous sand mixtures. Similarly, the use of the number-averaged sizes for the heterogeneous porous media produced a uniform relationship between the colloid straining capacity term (λ) and the ratio of d(p)/d(g) for all the sand treatments.

  20. Gravitational compression of colloidal gels

    NASA Astrophysics Data System (ADS)

    Liétor-Santos, J. J.; Kim, C.; Lu, P. J.; Fernández-Nieves, A.; Weitz, D. A.

    2009-02-01

    We study the compression of depletion gels under the influence of a gravitational stress by monitoring the time evolution of the gel interface and the local volume fraction, φ , inside the gel. We find φ is not constant throughout the gel. Instead, there is a volume fraction gradient that develops and grows along the gel height as the compression process proceeds. Our results are correctly described by a non-linear poroelastic model that explicitly incorporates the φ -dependence of the gravitational, elastic and viscous stresses acting on the gel.

  1. Two-Dimensional Colloidal Alloys

    NASA Astrophysics Data System (ADS)

    Law, Adam D.; Buzza, D. Martin A.; Horozov, Tommy S.

    2011-03-01

    We study the structure of mixed monolayers of large (3μm diameter) and small (1μm diameter) very hydrophobic silica particles at an octane-water interface as a function of the number fraction of small particles ξ. We find that a rich variety of two-dimensional hexagonal super-lattices of large (A) and small (B) particles can be obtained in this system due to strong and long-range electrostatic repulsions through the nonpolar octane phase. The structures obtained for the different compositions are in good agreement with zero temperature calculations and finite temperature computer simulations.

  2. Two-dimensional colloidal alloys.

    PubMed

    Law, Adam D; Buzza, D Martin A; Horozov, Tommy S

    2011-03-25

    We study the structure of mixed monolayers of large (3 μm diameter) and small (1 μm diameter) very hydrophobic silica particles at an octane-water interface as a function of the number fraction of small particles ξ. We find that a rich variety of two-dimensional hexagonal super-lattices of large (A) and small (B) particles can be obtained in this system due to strong and long-range electrostatic repulsions through the nonpolar octane phase. The structures obtained for the different compositions are in good agreement with zero temperature calculations and finite temperature computer simulations.

  3. The role of colloidal plasmonic nanostructures in organic solar cells.

    PubMed

    Singh, C R; Honold, T; Gujar, T P; Retsch, M; Fery, A; Karg, M; Thelakkat, M

    2016-08-17

    Plasmonic particles can contribute via multiple processes to the light absorption process in solar cells. These particles are commonly introduced into organic solar cells via deposition techniques such as spin-coating or dip-coating. However, such techniques are inherently challenging to achieve homogenous surface coatings as they lack control of inter-particle spacing and particle density on larger areas. Here we introduce interface assisted colloidal self-assembly as a concept for the fabrication of well-defined macroscopic 2-dimensional monolayers of hydrogel encapsulated plasmonic gold nanoparticles. The monolayers showed a pronounced extinction in the visible wavelength range due to localized surface plasmon resonance with excellent optical homogeneity. Moreover this strategy allowed for the investigation of the potential of plasmonic monolayers at different interfaces of P3HT:PCBM based inverted organic solar cells. In general, for monolayers located anywhere underneath the active layer, the solar cell performance decreased due to parasitic absorption. However with thick active layers, where low hole mobility limited the charge transport to the top electrode, the plasmonic monolayer near that electrode spatially redistributed the light and charge generation close to the electrode led to an improved performance. This work systematically highlights the trade-offs that need to be critically considered for designing an efficient plasmonically enhanced organic solar cell.

  4. Imaging grain boundary grooves in hard-sphere colloidal bicrystals

    NASA Astrophysics Data System (ADS)

    Maire, Eric; Redston, Emily; Persson Gulda, Maria; Weitz, David A.; Spaepen, Frans

    2016-10-01

    Colloidal particles were sedimented onto patterned glass slides to grow three-dimensional bicrystals with a controlled structure. Three types of symmetric tilt grain boundaries between close-packed face-centered-cubic crystals were produced: Σ 5 (100 ),Σ 17 (100 ) , and Σ 3 (110 ) . The structure of the crystals and their defects were visualized by confocal microscopy, and characterized by simple geometric measurements, including image difference, thresholding, and reprojection. This provided a quick and straightforward way to detect the regions in which the atoms are mobile. This atomic mobility was higher at the grain boundaries and close to the solid-liquid interface. This method was compared to the more conventional analysis based on the calculation of the local order parameter of the individual particles to identify the interface. This was used in turn to identify the presence of grooves at the grain-boundary-liquid triple junction for every type of grain boundary, except for the twin [Σ 3 (110 )] , for which no groove could be detected. Images of these grooves were processed, and the angle linking the grain boundary energy to the solid-liquid interfacial energy was measured. The resulting values of the grain boundary energy were compared to estimates based on the density deficit in the boundary.

  5. Pair Potential of Charged Colloidal Stars

    NASA Astrophysics Data System (ADS)

    Huang, F.; Addas, K.; Ward, A.; Flynn, N. T.; Velasco, E.; Hagan, M. F.; Dogic, Z.; Fraden, S.

    2009-03-01

    We report on the construction of colloidal stars: 1μm polystyrene beads grafted with a dense brush of 1μm long and 10 nm wide charged semiflexible filamentous viruses. The pair interaction potentials of colloidal stars are measured using an experimental implementation of umbrella sampling, a technique originally developed in computer simulations in order to probe rare events. The influence of ionic strength and grafting density on the interaction is measured. Good agreements are found between the measured interactions and theoretical predictions based upon the osmotic pressure of counterions.

  6. 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

  7. 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.

  8. 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.

  9. 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.

  10. Anisotropic elasticity of experimental colloidal Wigner crystals.

    PubMed

    Russell, Emily R; Spaepen, Frans; Weitz, David A

    2015-03-01

    Colloidal particles interacting via a long-range repulsion can, in contrast to hard-sphere systems, exhibit crystalline ordering at low volume fraction. Here we experimentally investigate the structure and properties of such "colloidal Wigner crystals." We find a body-centered-cubic crystalline phase at volume fractions of ϕ≳15%, which exhibits large fluctuations of individual particles from their average positions. We determine the three independent crystalline elastic constants and find that these crystals are very compliant and highly anisotropic.

  11. 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.

  12. 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)

  13. 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.

  14. 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.

  15. Novel Colloidal and Dynamic Interfacial Phenomena in Liquid Crystalline Systems

    DTIC Science & Technology

    2014-09-13

    investigation supported by this grant moved beyond past studies of interfacial and colloidal phenomena involving isotropic liquids to explore and understand a...2010 20-May-2014 Approved for Public Release; Distribution Unlimited Final Report: Novel Colloidal and Dynamic Interfacial Phenomena in Liquid...Army Research Office P.O. Box 12211 Research Triangle Park, NC 27709-2211 liquid crystals, interfacial phenomena, colloids , amphiphiles

  16. 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

  17. Interface resistance

    NASA Astrophysics Data System (ADS)

    Sinkkonen, Juha

    1983-11-01

    Interface resistance is studied by using the Landauer formula which relates the resistance to the quantum mechanical transmission coefficient. A simple rederivation of the Landauer formula is given. Using a step-like potential barrier as a model for the metal-semiconductor contact an analytical expression for the effective Richardson constant is derived. As an other application the grain boundary resistance in polycrystalline semiconductors is studied. The short-range potential fluctuation associated with the grain boundary is described by a rectangular potential barrier. The results for the grain boundary limited mobility cover both the strong and weak scattering regimes.

  18. 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

  19. Colloid Transport in Porous Medium: Impact of High Salinity Solutions

    NASA Astrophysics Data System (ADS)

    Weisbrod, N.; Magal, E.; Yechieli, Y.; Yakirevich, A.

    2009-12-01

    We explored the transport of colloids suspended in natural saline solutions with a wide range of ionic strengths, up to Dead Sea brines. Migration of latex microspheres through saturated sand columns of different sizes was studied in lab experiments, and colloid transport was simulated with a mathematical model. We have found that latex microspheres were mobile even in the extremely saline brines of the Dead Sea (ionic strength = 100.9 M). At this high ionic strength, according to the common colloid transport theories, no energetic barrier to colloid attachment exists and colloid adsorption was expected to be a favorable process. Apparently, even in that high salinity, colloids adsorption is not complete and ~20% colloids are allowed to transport (through 30-cm long column). Colloid transport was found to be related to the solution salinity, as expected. After 2-3 pore volumes (PV) the relative concentration of colloids at the outlet of 30-cm long columns decreased as the solution ionic strength increased until some critical value (ionic strength greater than 10-1.8 M) and then remained constant as the solution salinity increased. To further explore the sorption of colloids on sand surfaces in Dead Sea brines, breakthrough curves (BTCs) were studied using 7-cm long columns, through which hundreds of PV were introduced. The observed BTCs exhibited a bi-modal shape that suggests different rates of colloid attachment. After initial breakthrough the relative concentration of colloids at the outlet rose to a value of 0.8 (after 1.5 PV), and it remained relatively constant until approximately 17 PV were flushed through the column. After a total flow of about 20 PV, the relative concentration reached a value of one. The colloid migration process was successfully modeled using the limited entrapment model (Pachepsky et al., 2006), assuming the colloid attachment rate is dependent on the concentration of attached colloids.

  20. Measuring colloidal osmotic compressibility of a polymer-crowded colloidal suspension by optical trapping

    NASA Astrophysics Data System (ADS)

    Fu, Jinxin; Kara, Vural; Ou-Yang, H. Daniel

    2013-03-01

    Particle interactions determine the stability of nanoparticle suspensions and the phase separation of particle-polymer mixtures. However, due to the small sizes of the dispersed nanoparticles, it is not easy to directly measure interaction forces between particles in a colloidal suspension. In this paper, we propose an ``Optical Bottle'' approach to quantify these particle interactions in a suspension by measuring the colloidal osmotic compressibility of the nanoparticles. Virial expansion of the colloidal osmotic compressibility yields virial coefficients of different orders. The second order virial coefficient of aqueous suspensions of colloidal polystyrene nanospheres in the presence of high-salt (KCl) and polyethylene glycol (PEG) is found to decrease with increasing PEG concentration, suggesting an attractive depletion interaction between the PEG-crowed polystyrene particles.

  1. Detachment energies of spheroidal particles from fluid-fluid interfaces

    NASA Astrophysics Data System (ADS)

    Davies, Gary B.; Krüger, Timm; Coveney, Peter V.; Harting, Jens

    2014-10-01

    The energy required to detach a single particle from a fluid-fluid interface is an important parameter for designing certain soft materials, for example, emulsions stabilised by colloidal particles, colloidosomes designed for targeted drug delivery, and bio-sensors composed of magnetic particles adsorbed at interfaces. For a fixed particle volume, prolate and oblate spheroids attach more strongly to interfaces because they have larger particle-interface areas. Calculating the detachment energy of spheroids necessitates the difficult measurement of particle-liquid surface tensions, in contrast with spheres, where the contact angle suffices. We develop a simplified detachment energy model for spheroids which depends only on the particle aspect ratio and the height of the particle centre of mass above the fluid-fluid interface. We use lattice Boltzmann simulations to validate the model and provide quantitative evidence that the approach can be applied to simulate particle-stabilized emulsions, and highlight the experimental implications of this validation.

  2. Size determinations of plutonium colloids using autocorrelation photon spectroscopy

    SciTech Connect

    Triay, I.R.; Rundberg, R.S.; Mitchell, A.J.; Ott, M.A.; Hobart, D.E.; Palmer, P.D.; Newton, T.W.; Thompson, J.L.

    1989-12-01

    Autocorrelation Photon Spectroscopy (APS) is a light-scattering technique utilized to determine the size distribution of colloidal suspensions. The capabilities of the APS methodology have been assessed by analyzing colloids of known sizes. Plutonium(IV) colloid samples were prepared by a variety of methods including: dilution; peptization; and alpha-induced auto-oxidation of Pu(III). The size of theses Pu colloids was analyzed using APS. The sizes determined for the Pu colloids studied varied from 1 to 370 nanometers. 7 refs., 5 figs., 3 tabs.

  3. Preparation of iridescent colloidal crystal coatings with variable structural colors.

    PubMed

    Cong, Hailin; Yu, Bing; Wang, Shaopeng; Qi, Limin; Wang, Jilei; Ma, Yurong

    2013-07-29

    Iridescent colloidal crystal coatings with variable structural colors were fabricated by incorporating carbon black nanoparticles (CB-NPs) into the voids of polystyrene (PS) colloidal crystals. The structural color of the colloid crystal coatings was not only greatly enhanced after the composition but also varied with observation angles. By changing the diameter of monodisperse PS colloids in the composites, colloidal crystal coatings with three primary colors for additive or subtractive combination were obtained. After incorporation of the PS/CB-NPs hybrid coatings into polydimethylsiloxane (PDMS) matrix, manmade opal jewelry with variable iridescent colors was made facilely.

  4. 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.

  5. Aggregation kinetics of coalescing polymer colloids.

    PubMed

    Gauer, Cornelius; Jia, Zichen; Wu, Hua; Morbidelli, Massimo

    2009-09-01

    The aggregation behavior of a soft, rubbery colloidal system with a relatively low glass transition temperature, T(g) approximately -20 degrees C, has been investigated. It is found that the average gyration and hydrodynamic radii, R(g) and R(h), measured by light scattering techniques, evolve in time in parallel, without exhibiting the crossover typical of rigid particle aggregation. Cryogenic scanning electron microscopy (cryo-SEM) images reveal sphere-like clusters, indicating that complete coalescence between particles occurs during aggregation. Since coalescence leads to a reduction in the total colloidal surface area, the surfactant adsorption equilibrium, and thus the colloidal stability, change in the course of aggregation. It is found that to simulate the observed kinetic behavior based on the population balance equations, it is necessary to assume that all the clusters are spherical and to account for variations in the colloidal stability of each aggregating particle pair with time. This indicates that, for the given system, the coalescence is very fast, i.e., its time scale is much smaller than that of the aggregation.

  6. 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.

  7. 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.

  8. 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.

  9. Electroneutrality and phase behavior of colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Denton, A. R.

    2007-11-01

    Several statistical mechanical theories predict that colloidal suspensions of highly charged macroions and monovalent microions can exhibit unusual thermodynamic phase behavior when strongly deionized. Density-functional, extended Debye-Hückel, and response theories, within mean-field and linearization approximations, predict a spinodal phase instability of charged colloids below a critical salt concentration. Poisson-Boltzmann cell model studies of suspensions in Donnan equilibrium with a salt reservoir demonstrate that effective interactions and osmotic pressures predicted by such theories can be sensitive to the choice of reference system, e.g., whether the microion density profiles are expanded about the average potential of the suspension or about the reservoir potential. By unifying Poisson-Boltzmann and response theories within a common perturbative framework, it is shown here that the choice of reference system is dictated by the constraint of global electroneutrality. On this basis, bulk suspensions are best modeled by density-dependent effective interactions derived from a closed reference system in which the counterions are confined to the same volume as the macroions. Lower-dimensional systems (e.g., monolayers, clusters), depending on the strength of macroion-counterion correlations, may be governed instead by density-independent effective interactions tied to an open reference system with counterions dispersed throughout the reservoir, possibly explaining the observed structural crossover in colloidal monolayers and anomalous metastability of colloidal crystallites.

  10. Practical colloidal processing of multication ceramics

    DOE PAGES

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

    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. 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.

  12. Stratification dynamics in drying colloidal mixtures.

    PubMed

    Howard, Michael P; Nikoubashman, Arash; Panagiotopoulos, Athanassios Z

    2017-03-28

    Stratification in binary colloidal mixtures was investigated using implicit-solvent molecular dynamics simulations. For large particle size ratios and film Péclet numbers greater than unity, smaller colloids migrated to the top of the film, while big colloids were pushed to the bottom, creating an "inverted" stratification. This peculiar behavior was observed in recent simulations and experiments conducted by Fortini et al. (Phys. Rev. Lett. 2016, 116, 118301). To rationalize this behavior, particle size ratios and drying rates spanning qualitatively different Péclet number regimes were systematically studied, and the dynamics of the inverted stratification were quantified in detail. The stratified layer of small colloids was found to grow faster and to larger thicknesses for larger size ratios. Interestingly, inverted stratification was observed even at moderate drying rates where the film Péclet numbers were comparable to unity, but the thickness of the stratified layer decreased. A model based on dynamical density functional theory is proposed to explain the observed phenomena.

  13. Forces between colloid particles in natural waters.

    PubMed

    Mosley, Luke M; Hunter, Keith A; Ducker, William A

    2003-08-01

    The origin and nature of interparticle forces acting on colloid surfaces in natural waters has been examined using an atomic force microscope. Natural colloids were represented by a surface film of iron oxide precipitated onto spherical SiO2 particles, and the effects of adsorbed natural organic matter (NOM), solution pH, and ionic composition on the force-separation curves were investigated. NOM from both riverine and marine environments was strongly adsorbed to the iron oxide surface. Under conditions of low ionic strength, the interparticle forces were dominated by electrostatic repulsion arising from negative functional groups on the NOM, except at very small separations (<10 nm) where repulsive forces arising from steric interference of the NOM molecules were also present. At high ionic strength (e.g., seawater) or low pH, the electrostatic forces were largely absent, allowing steric repulsion forces to dominate. In addition, adhesive bridging between surfaces by adsorbed NOM was observed, creating a strong energy barrier to spontaneous disaggregation of colloid aggregates. Our results demonstrate that adsorbed NOM dominates the surface forces and thus stability with respect to aggregation of natural water colloids.

  14. Colloidal nanophotonics: the emerging technology platform.

    PubMed

    Gaponenko, Sergey; Demir, Hilmi Volkan; Seassal, Christian; Woggon, Ulrike

    2016-01-25

    Dating back to decades or even centuries ago, colloidal nanophotonics during the last ten years rapidly extends towards light emitting devices, lasers, sensors and photonic circuitry to manifest itself as an emerging technology platform rather than an entirely academic research field.

  15. 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.

  16. 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.

  17. Rheology and dynamics of colloidal superballs.

    PubMed

    Royer, John R; Burton, George L; Blair, Daniel L; Hudson, Steven D

    2015-07-28

    Recent advances in colloidal synthesis make it possible to generate a wide array of precisely controlled, non-spherical particles. This provides a unique opportunity to probe the role that particle shape plays in the dynamics of colloidal suspensions, particularly at higher volume fractions, where particle interactions are important. We examine the role of particle shape by characterizing both the bulk rheology and micro-scale diffusion in a suspension of pseudo-cubic silica superballs. Working with these well-characterized shaped colloids, we can disentangle shape effects in the hydrodynamics of isolated particles from shape-mediated particle interactions. We find that the hydrodynamic properties of isolated superballs are marginally different from comparably sized hard spheres. However, shape-mediated interactions modify the suspension microstructure, leading to significant differences in the self-diffusion of the superballs. While this excluded volume interaction can be captured with a rescaling of the superball volume fraction, we observe qualitative differences in the shear thickening behavior of moderately concentrated superball suspensions that defy simple rescaling onto hard sphere results. This study helps to define the unknowns associated with the effects of shape on the rheology and dynamics of colloidal solutions.

  18. Continuous separation of colloidal particles using dielectrophoresis.

    PubMed

    Yunus, Nurul Amziah Md; Nili, Hossein; Green, Nicolas G

    2013-04-01

    Dielectrophoresis is the movement of particles in nonuniform electric fields and has been of interest for application to manipulation and separation at and below the microscale. This technique has the advantages of being noninvasive, nondestructive, and noncontact, with the movement of particle achieved by means of electric fields generated by miniaturized electrodes and microfluidic systems. Although the majority of applications have been above the microscale, there is increasing interest in application to colloidal particles around a micron and smaller. This paper begins with a review of colloidal and nanoscale dielectrophoresis with specific attention paid to separation applications. An innovative design of integrated microelectrode array and its application to flow-through, continuous separation of colloidal particles is then presented. The details of the angled chevron microelectrode array and the test microfluidic system are then discussed. The variation in device operation with applied signal voltage is presented and discussed in terms of separation efficiency, demonstrating 99.9% separation of a mixture of colloidal latex spheres.

  19. Preparation and properties of uniform size colloids

    SciTech Connect

    Matijevic, E. )

    1993-04-01

    The achievements and problems in the preparation of uniform colloids by precipitation from homogeneous electrolyte solutions are reviewed. Specifically, the syntheses of [open quotes]monodispersed[close quotes] particles of simple and mixed compositions as well as of coated and hollow particles of different shapes are described, and the physical and chemical mechanisms of their formation are discussed. 126 refs., 25 figs., 1 tab.

  20. 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.

  1. 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

  2. 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.

  3. 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.

  4. Active structuring of colloidal armour on liquid drops

    PubMed Central

    Dommersnes, Paul; Rozynek, Zbigniew; Mikkelsen, Alexander; Castberg, Rene; Kjerstad, Knut; Hersvik, Kjetil; Otto Fossum, Jon

    2013-01-01

    Adsorption and assembly of colloidal particles at the surface of liquid droplets are at the base of particle-stabilized emulsions and templating. Here we report that electrohydrodynamic and electro-rheological effects in leaky-dielectric liquid drops can be used to structure and dynamically control colloidal particle assemblies at drop surfaces, including electric-field-assisted convective assembly of jammed colloidal ‘ribbons’, electro-rheological colloidal chains confined to a two-dimensional surface and spinning colloidal domains on that surface. In addition, we demonstrate the size control of ‘pupil’-like openings in colloidal shells. We anticipate that electric field manipulation of colloids in leaky dielectrics can lead to new routes of colloidosome assembly and design for ‘smart armoured’ droplets. PMID:23811716

  5. [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.

  6. Introduction to special section on Colloid Transport in Subsurface Environments

    NASA Astrophysics Data System (ADS)

    Saiers, James E.; Ryan, Joseph N.

    2006-12-01

    The Water Resources Research special section on Colloid Transport in Subsurface Environments presents new knowledge that is critical to solving problems related to groundwater pollution by microbial pathogens and hazardous chemicals. This introduction to the special section surveys fourteen manuscripts that advance current understanding of the transport of biocolloids (e.g., bacteria, viruses, and protozoa), mineral colloids, and colloid-associated contaminants in the vadose zone and in groundwater. These papers present new techniques for elucidating mechanisms that govern colloid mobility, propose mathematical models appropriate for quantifying colloid and colloid-associated contaminant transport, and report pore-scale and column-scale observations requisite for evaluating these models. Together, the papers of this special section illuminate the complexity of the colloid transport problem and describe progress toward understanding this complexity.

  7. 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.

  8. Amphiphilic crescent-moon-shaped microparticles formed by selective adsorption of colloids.

    PubMed

    Kim, Shin-Hyun; Abbaspourrad, Alireza; Weitz, David A

    2011-04-13

    We use a microfluidic device to prepare monodisperse amphiphilic particles in the shape of a crescent-moon and use these particles to stabilize oil droplets in water. The microfluidic device is comprised of a tapered capillary in a theta (θ) shape that injects two oil phases into water in a single receiving capillary. One oil is a fluorocarbon, while the second is a photocurable monomer, which partially wets the first oil drop; silica colloids in the monomer migrate and adsorb to the interface with water but do not protrude into the oil interface. Upon UV-induced polymerization, solid particles with the shape of a crescent moon are formed; removal of fluorocarbon oil yields amphiphilic particles due to the selective adsorption of silica colloids. The resultant amphiphilic microparticles can be used to stabilize oil drops in a mixture of water and ethanol; if they are packed to sufficient surface density on the interface of the oil drop, they become immobilized, preventing direct contact between neighboring drops, thereby providing the stability.

  9. Interface standardization

    NASA Technical Reports Server (NTRS)

    Spencer, R.; Wong, V.

    1983-01-01

    Central-station applications create a large and attractive market for photovoltaics in the near future. However, some significant barriers lie between the industry of today and realization of that market. Manufacturing capacity and price are two principal impediments. The Utilities, which are the future system owners, are gaining experience with central-station PV power through the Sacramento Municipal Utility District, Hesperia and similar small central-station installations. SMUD has recognized that competition must be maintained to help reduce prices. So little standardization exists that the cost is driven upward to redefine mechanical and electrical interfaces for each vendor. New structues are required for each vendor and nonoptimum field geometries result from attempts to include more than one vendor in an array field. Standards at some hardware level are required.

  10. A Landau-de Gennes theory for hard colloidal rods: Defects and tactoids

    NASA Astrophysics Data System (ADS)

    Everts, J. C.; Punter, M. T. J. J. M.; Samin, S.; van der Schoot, P.; van Roij, R.

    2016-05-01

    We construct a phenomenological Landau-de Gennes theory for hard colloidal rods by performing an order parameter expansion of the chemical-potential dependent grand potential. By fitting the coefficients to known results of Onsager theory, we are not only able to describe the isotropic-nematic phase transition as function of density, including the well-known density jump, but also the isotropic-nematic planar interface. The resulting theory is applied in calculations of the isotropic core size in a radial hedgehog defect, the density dependence of linear defects of hard rods in square confinement, and the formation of a nematic droplet in an isotropic background.

  11. Beyond Millikan: the dynamics of charging events on individual colloidal particles.

    PubMed

    Beunis, Filip; Strubbe, Filip; Neyts, Kristiaan; Petrov, Dmitri

    2012-01-06

    By measuring the stable charge on oil drops in air, Millikan demonstrated the discrete nature of electric charge. We extend his approach to the charge on solid-liquid interfaces, and focus on the dynamics of the discrete fluctuations. Our measurements are accurate and fast enough to observe changes of one elementary charge. Experiments over thousands of seconds yield information about the fast dynamics of electrochemical reactions, relevant for physicochemical and biological systems. As an example, we study (dis)charging processes on colloidal particles in a nonpolar liquid.

  12. Beyond Millikan: The Dynamics of Charging Events on Individual Colloidal Particles

    NASA Astrophysics Data System (ADS)

    Beunis, Filip; Strubbe, Filip; Neyts, Kristiaan; Petrov, Dmitri

    2012-01-01

    By measuring the stable charge on oil drops in air, Millikan demonstrated the discrete nature of electric charge. We extend his approach to the charge on solid-liquid interfaces, and focus on the dynamics of the discrete fluctuations. Our measurements are accurate and fast enough to observe changes of one elementary charge. Experiments over thousands of seconds yield information about the fast dynamics of electrochemical reactions, relevant for physicochemical and biological systems. As an example, we study (dis)charging processes on colloidal particles in a nonpolar liquid.

  13. 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

  14. Monte Carlo simulations of the solid-liquid transition in hard spheres and colloid-polymer mixtures.

    PubMed

    Zykova-Timan, T; Horbach, J; Binder, K

    2010-07-07

    Monte Carlo simulations at constant pressure are performed to study coexistence and interfacial properties of the liquid-solid transition in hard spheres and in colloid-polymer mixtures. The latter system is described as a one-component Asakura-Oosawa (AO) model where the polymer's degrees of freedom are incorporated via an attractive part in the effective potential for the colloid-colloid interactions. For the considered AO model, the polymer reservoir packing fraction is eta(p) (r)=0.1 and the colloid-polymer size ratio is q[triple bond]sigma(p)/sigma=0.15 (with sigma(p) and sigma as the diameter of polymers and colloids, respectively). Inhomogeneous solid-liquid systems are prepared by placing the solid fcc phase in the middle of a rectangular simulation box, creating two interfaces with the adjoined bulk liquid. By analyzing the growth of the crystalline region at various pressures and for different system sizes, the coexistence pressure p(co) is obtained, yielding p(co)=11.576 k(B)T/sigma(3) for the hard-sphere system and p(co)=8.00 k(B)T/sigma(3) for the AO model (with k(B) as the Boltzmann constant and T as the temperature). Several order parameters are introduced to distinguish between solid and liquid phases and to describe the interfacial properties. From the capillary-wave broadening of the solid-liquid interface, the interfacial stiffness is obtained for the (100) crystalline plane, giving the values gamma approximately 0.49 k(B)T/sigma(2) for the hard-sphere system and gamma approximately 0.95 k(B)T/sigma(2) for the AO model.

  15. Monte Carlo simulations of the solid-liquid transition in hard spheres and colloid-polymer mixtures

    NASA Astrophysics Data System (ADS)

    Zykova-Timan, T.; Horbach, J.; Binder, K.

    2010-07-01

    Monte Carlo simulations at constant pressure are performed to study coexistence and interfacial properties of the liquid-solid transition in hard spheres and in colloid-polymer mixtures. The latter system is described as a one-component Asakura-Oosawa (AO) model where the polymer's degrees of freedom are incorporated via an attractive part in the effective potential for the colloid-colloid interactions. For the considered AO model, the polymer reservoir packing fraction is ηpr=0.1 and the colloid-polymer size ratio is q ≡σp/σ=0.15 (with σp and σ as the diameter of polymers and colloids, respectively). Inhomogeneous solid-liquid systems are prepared by placing the solid fcc phase in the middle of a rectangular simulation box, creating two interfaces with the adjoined bulk liquid. By analyzing the growth of the crystalline region at various pressures and for different system sizes, the coexistence pressure pco is obtained, yielding pco=11.576 kBT/σ3 for the hard-sphere system and pco=8.00 kBT/σ3 for the AO model (with kB as the Boltzmann constant and T as the temperature). Several order parameters are introduced to distinguish between solid and liquid phases and to describe the interfacial properties. From the capillary-wave broadening of the solid-liquid interface, the interfacial stiffness is obtained for the (100) crystalline plane, giving the values γ˜≈0.49 kBT/σ2 for the hard-sphere system and γ˜≈0.95 kBT/σ2 for the AO model.

  16. 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

  17. 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

  18. Temporally Anticorrelated Motion of Nanoparticles at a Liquid Interface.

    PubMed

    Wang, Dapeng; Hu, Renfeng; Skaug, Michael J; Schwartz, Daniel K

    2015-01-02

    Quantum dots at the hexane-glycerol interface exhibited unexpected behavior including highly dynamic adsorption/desorption, where the lateral nanoparticle motion was anomalously fast immediately after adsorption and prior to desorption. At the interface, particles exhibited pseudo-Brownian lateral motion, in which the instantaneous diffusion coefficient was temporally anticorrelated, in agreement with our simulations involving fractional Brownian motion in the surface-normal direction. These phenomena suggest that, in contrast to the conventional picture for colloidal particles, nanoparticles explore a landscape of metastable interfacial positions, with different exposures to the two adjacent phases.

  19. And yet it moves - propulsion of colloidal clusters under reciprocal actuation

    NASA Astrophysics Data System (ADS)

    Steinbach, Gabi; Gemming, Sibylle; Erbe, Artur

    In the regime of low Reynolds numbers, the challenge of torque-based magnetic actuation lies in the conversion of torque into an effective force via symmetry breaking without inertial effects. Most reported systems rely on the hydrodynamic coupling between rotation and translation by an asymmetry in the environment (surfaces/interfaces) or the object shape. There, net translation can be realized only under non-reciprocal actuation given by precessing and rotating fields. In contrast, under oscillating fields, which are easier to realize, hydrodynamic coupling intrinsically leads to cyclic, reciprocal translation (Scallop theorem) unless the object has a certain flexible shape such as a flagellum. We present an alternative approach where symmetry breaking can be realized by magnetically interacting colloids which have been effectively modeled by spheres with shifted dipoles. If such colloids self-assemble, they form rigid clusters. We show how the collective, non-equilibrium dynamics of the colloids under oscillating fields propel the cluster. Depending on the configuration of the cluster it can rotate, translate and perform screw-like motion. Grants funding by DFG: FOR 1713 GE 1202/9-1 and ER 341/9-1.

  20. Surface functionalized LSMO nanoparticles with improved colloidal stability for hyperthermia applications

    NASA Astrophysics Data System (ADS)

    Thorat, N. D.; Khot, V. M.; Salunkhe, A. B.; Prasad, A. I.; Ningthoujam, R. S.; Pawar, S. H.

    2013-03-01

    LSMO (La0.7Sr0.3MnO3) magnetic nanoparticles (MNPs) coated with double layer oleic acid (OA) surfactant are prepared to make a water based magnetic nanofluid for hyperthermia application. Various experimental techniques are used for bilayer coating analysis. The effect of the bilayer coating on magnetic properties is studied by superconducting quantum interface device (SQUID). Colloidal behaviour of coated MNPs in aqueous medium is studied by the zeta potential and dynamic light scattering. The effects of pH and ionic strength on the colloidal stability of the MNPs are studied in detail. For the bilayer-coated LSMO MNPs aggregation is not observed even in high ionic strength and at physiological pH (7.4). For making the nanofluid of the bilayer-coated MNPs the colloidal stability is studied in physiological media like phosphate buffer solution. Under induction heating experiment, hyperthermia temperature (42-43 °C) could be achieved by the bilayer-coated sample at a magnetic field of 168-335 Oe and frequency of 267 kHz. The bilayer OA coating can hinder the agglomeration of MNPs significantly and produce stable suspension with improved hyperthermia properties. The bilayer OA coating also improves the specific absorption rate (SAR) of LSMO MNPs from 25 to 40 W g-1.

  1. 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.

  2. Sorption of selected endocrine disrupting chemicals to different aquatic colloids.

    PubMed

    Zhou, J L; Liu, R; Wilding, A; Hibberd, A

    2007-01-01

    The sorption of seven endocrine disrupting chemicals (EDCs) to aquatic colloids was determined by cross-flow ultrafiltration (CFUF) followed by gas chromatography-mass spectrometry (GC-MS). Results show that the colloidal organic carbon normalized sorption coefficient (Kcoc) of EDCs to different aquatic colloids varies by a factor of 6-12 because such colloids are of different origin. Through characterization of colloidal samples, a significant relationship was established between Kcoc values and the molar extinction coefficient of colloids at 280 nm, whereas no other colloidal properties such as elemental ratios were correlated with Kcoc values. The results are consistent with other reports of the importance of the quality of sorbents such as their aromatic carbon content in sorbing various organic pollutants. The presence of a surfactant was found to increase Kcoc values for estrone (El) and 17alpha-ethynylestradiol (EE2). The method was subsequently applied for determining EDC concentrations in field samples, where both conventional and truly dissolved EDCs showed higher concentrations close to sewage outfalls than either upstream or downstream, confirming the sourceconcentration relationship. In addition, the truly dissolved EDC concentrations were lower than the conventional dissolved concentrations, confirming that there were interactions between aquatic colloids and EDCs. It is estimated that between 10 and 29% of EDCs are associated with aquatic colloids. As colloids are highly abundant in rivers and ocean, they will therefore play a significant role in the environmental behavior and fate of EDCs.

  3. 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.

  4. 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.

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

    PubMed

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

    2015-01-01

    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 pH7 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.

  6. Colloidal Dancers: Designing networks of DNA-functionalized colloids for non-random walks

    NASA Astrophysics Data System (ADS)

    Gehrels, Emily W.; Rogers, W. Benjamin; Zeravcic, Zorana; Manoharan, Vinothan N.

    2014-03-01

    We present experimental developments of a system of DNA-functionalized colloidal particles with the goal of creating directed motion (`dancing') along patterned substrates in response to temperature cycling. We take advantage of toehold exchange in the design of the DNA sequences that mediate the colloidal interactions to produce broadened, flat, or even re-entrant binding and unbinding transitions between the particles and substrate. Using this new freedom of design, we devise systems where, by thermal ratcheting, we can externally control the direction of motion and sequence of steps of the colloidal dancer. In comparison to DNA-based walkers, which move autonomously and whose motion is controlled by the substrate, our colloidal dancers respond to external driving, and their motion can be controlled in situ. Our use of DNA-functionalized colloidal particles instead of pure DNA systems also enables walking on the mesoscale in contrast to the molecular length scales previously demonstrated, allowing for the future prospect of directed transport over larger distances.

  7. Tunable Assembly of Heterogeneously Charged Colloids

    PubMed Central

    2014-01-01

    The self-assembly of colloidal particles is a route to designed materials production that combines high flexibility, cost effectiveness, and the opportunity to create ordered structures at length scales ranging from nano- to micrometers. For many practical applications in electronics, photovoltaics, and biomimetic material synthesis, ordered mono- and bilayers are often needed. Here we present a novel and simple way to tune via external parameters the ordering of heterogeneously charged colloids into quasi two-dimensional structures. Depending on the charges of the underlying substrate and of the particles, a rich and versatile assembly scenario takes place, resulting from the complex interplay between directional attractive and repulsive particle–particle and particle–substrate interactions. Upon subtle variations of the relative charge of the system components, emerging via pH modification, reversible changes either from extended aggregates to a monomeric phase or from triangular to square domains are observed. PMID:24842542

  8. Renormalized jellium model for colloidal mixtures

    NASA Astrophysics Data System (ADS)

    García de Soria, María Isabel; Álvarez, Carlos E.; Trizac, Emmanuel

    2016-10-01

    In an attempt to quantify the role of polydispersity in colloidal suspensions, we present an efficient implementation of the renormalized jellium model for a mixture of spherical charged colloids. The different species may have different size, charge, and density. Advantage is taken from the fact that the electric potential pertaining to a given species obeys a Poisson's equation that is species independent; only boundary conditions do change from one species to the next. All species are coupled through the renormalized background (jellium) density, that is determined self-consistently. The corresponding predictions are compared to the results of Monte Carlo simulations of binary mixtures, where Coulombic interactions are accounted for exactly, at the primitive model level (structureless solvent with fixed dielectric permittivity). An excellent agreement is found.

  9. 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.

  10. Correlated Clusters in Aging Colloidal Glass

    NASA Astrophysics Data System (ADS)

    Robe, Dominic; Boettcher, Stefan; Yunker, Peter

    A numerical model of correlated domains in glassy colloids is recreated, following its development by Becker, et. al.. The model is a course grained representation of 2D colloidal systems inspired by record dynamics, and produces emergent dynamic heterogeneity and aging. Results from the original development are reproduced, and compared to the same observables in an experimental system of bidisperse microgel spheres studied by Yunker, et. al.. Basic observables such as particle persistence and mean square displacement are measured at different waiting times to observe aging. Four-point correlation lengths are also examined for signs of dynamic heterogeneity. Results from both the numerical and experimental systems are consistent with the predictions of record dynamics, that aging systems evolve on a logarithmic time scale. This work is supported by NSF Grant DMR-1207431.

  11. Hybrid colloidal plasmonic-photonic crystals.

    PubMed

    Romanov, Sergei G; Korovin, Alexander V; Regensburger, Alois; Peschel, Ulf

    2011-06-17

    We review the recently emerged class of hybrid metal-dielectric colloidal photonic crystals. The hybrid approach is understood as the combination of a dielectric photonic crystal with a continuous metal film. It allows to achieve a strong modification of the optical properties of photonic crystals by involving the light scattering at electronic excitations in the metal component into moulding of the light flow in series to the diffraction resonances occurring in the body of the photonic crystal. We consider different realizations of hybrid plasmonic-photonic crystals based on two- and three-dimensional colloidal photonic crystals in association with flat and corrugated metal films. In agreement with model calculations, different resonance phenomena determine the optical response of hybrid crystals leading to a broadly tuneable functionality of these crystals.

  12. 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

  13. 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

  14. 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.

  15. 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.

  16. 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.

  17. Forging Colloidal Nanostructures via Cation Exchange Reactions

    PubMed Central

    2016-01-01

    Among the various postsynthesis treatments of colloidal nanocrystals that have been developed to date, transformations by cation exchange have recently emerged as an extremely versatile tool that has given access to a wide variety of materials and nanostructures. One notable example in this direction is represented by partial cation exchange, by which preformed nanocrystals can be either transformed to alloy nanocrystals or to various types of nanoheterostructures possessing core/shell, segmented, or striped architectures. In this review, we provide an up to date overview of the complex colloidal nanostructures that could be prepared so far by cation exchange. At the same time, the review gives an account of the fundamental thermodynamic and kinetic parameters governing these types of reactions, as they are currently understood, and outlines the main open issues and possible future developments in the field. PMID:26891471

  18. Restricted Defect Dynamics in Colloidal Peanut Crystals

    NASA Astrophysics Data System (ADS)

    Gerbode, Sharon; Lee, Stephanie; John, Bettina; Wolfgang, Angie; Liddell, Chekesha; Escobedo, Fernando; Cohen, Itai

    2008-03-01

    We report that monolayers of hard peanut-shaped colloidal particles consisting of two connected spherical lobes order into a crystalline phase at high area fractions. In this ``lobe-close-packed'' (LCP) crystal, the peanut particle lobes occupy triangular lattice sites, much like close-packed spheres, while the connections between lobe pairs are randomly oriented, uniformly populating the three crystalline directions of the underlying lattice. Using optical microscopy, we directly observe defect nucleation and dynamics in sheared LCP crystals. We find that many particle configurations form obstacles blocking dislocation glide. Consequently, in stark contrast to colloidal monolayers of close-packed spheres, single dislocation pair nucleation is not the only significant energetic barrier to relieving an imposed shear strain. Dislocation propagation beyond such obstructions can proceed only through additional mechanisms such as dislocation reactions. We discuss the implications of such restricted defect mobility for the plasticity of LCP crystals.

  19. Restricted Defect Dynamics in Colloidal Peanut Crystals

    NASA Astrophysics Data System (ADS)

    Gerbode, Sharon; Lee, Stephanie; John, Bettina; Wolfgang, Angie; Liddell, Chakesha; Escobedo, Fernando; Cohen, Itai

    2008-03-01

    We report that monolayers of hard peanut-shaped colloidal particles consisting of two connected spherical lobes order into a crystalline phase at high area fractions. In this ``lobe- close-packed'' (LCP) crystal, the peanut particle lobes occupy triangular lattice sites, much like close-packed spheres, while the connections between lobe pairs are randomly oriented, uniformly populating the three crystalline directions of the underlying lattice. Using optical microscopy, we directly observe defect nucleation and dynamics in sheared LCP crystals. We find that many particle configurations form obstacles blocking dislocation glide. Consequently, in stark contrast to colloidal monolayers of close-packed spheres, single dislocation pair nucleation is not the only significant energetic barrier to relieving an imposed shear strain. Dislocation propagation beyond such obstructions can proceed only through additional mechanisms such as dislocation reactions. We discuss the implications of such restricted defect mobility for the plasticity of LCP crystals.

  20. Colloidal cholesteric liquid crystal in spherical confinement

    NASA Astrophysics Data System (ADS)

    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

    2016-08-01

    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.

  1. Renormalized jellium model for colloidal mixtures.

    PubMed

    García de Soria, María Isabel; Álvarez, Carlos E; Trizac, Emmanuel

    2016-10-01

    In an attempt to quantify the role of polydispersity in colloidal suspensions, we present an efficient implementation of the renormalized jellium model for a mixture of spherical charged colloids. The different species may have different size, charge, and density. Advantage is taken from the fact that the electric potential pertaining to a given species obeys a Poisson's equation that is species independent; only boundary conditions do change from one species to the next. All species are coupled through the renormalized background (jellium) density, that is determined self-consistently. The corresponding predictions are compared to the results of Monte Carlo simulations of binary mixtures, where Coulombic interactions are accounted for exactly, at the primitive model level (structureless solvent with fixed dielectric permittivity). An excellent agreement is found.

  2. 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

  3. Colloidal nanocrystals fluoresced by surface coordination complexes.

    PubMed

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

    2014-06-27

    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.

  4. Toward Multispectral Imaging with Colloidal Metasurface Pixels.

    PubMed

    Stewart, Jon W; Akselrod, Gleb M; Smith, David R; Mikkelsen, Maiken H

    2017-02-01

    Multispectral colloidal metasurfaces are fabricated that exhibit greater than 85% absorption and ≈100 nm linewidths by patterning film-coupled nanocubes in pixels using a fusion of bottom-up and top-down fabrication techniques over wafer-scale areas. With this technique, the authors realize a multispectral pixel array consisting of six resonances between 580 and 1125 nm and reconstruct an RGB image with 9261 color combinations.

  5. CGEL-2: Structural Studies of Colloidal Suspensions

    NASA Technical Reports Server (NTRS)

    2004-01-01

    These are images of CGEL-2 samples taken during STS-95. They show binary colloidal suspensions that have formed ordered crystalline structures in microgravity. In sample 5, there are more particles therefore, many, many crystallites (small crystals) form. In sample 6, there are less particles therefore, the particles are far apart and few, much larger crystallites form. The white object in the right corner of sample 5 is the stir bar used to mix the sample at the begirning of the mission.

  6. Stabilization of Colloidal Silica Using Small Polyols

    SciTech Connect

    GULLEY, GERALD L.; MARTIN, JAMES E.

    1999-09-07

    We have discovered that small polyols are reasonably effective at stabilizing colloidal silica against aggregation, even under the conditions of high pH and salt concentration. Both quasielastic and elastic light scattering were used to show that these polyols dramatically decrease the aggregation rate of the suspension, changing the growth kinetics from diffusion-limited cluster-cluster aggregation to reaction-limited cluster-cluster aggregation. These polyols maybe useful in the treatment of tank wastes at the Hanford site.

  7. Columnar self-assembly of colloidal nanodisks.

    PubMed

    Saunders, Aaron E; Ghezelbash, Ali; Smilgies, Detlef-M; Sigman, Michael B; Korgel, Brian A

    2006-12-01

    The self-assembly of sterically stabilized colloidal copper sulfide nanodisks, 14-20 nm in diameter and 5-7 nm thick, was studied. The nanodisks were observed by electron microscopy and small-angle X-ray scattering to form columnar arrays when evaporated as thin films from concentrated dispersions. These superstructured nanomaterials might give rise to technologically useful properties, such as anisotropic electrical transport and electrorheological and optical properties.

  8. Influence of biofilms on the movement of colloids in porous media. Implications for colloid facilitated transport in subsurface environments.

    PubMed

    Leon Morales, Carlos Felipe; Strathmann, Martin; Flemming, Hans-Curt

    2007-05-01

    Colloid transport through porous media can be influenced by the presence of biofilms. Sterile and non-sterile sand columns were investigated using Laponite RD as model colloid and a highly mucoid strain of Pseudomonas aeruginosa as model biofilm former. Laponite RD was marked specifically by fluorescent complexes with rhodamine 6G. Breakthrough curves (BTCs) were used as parameters for determination of colloid transport characteristics. In the sterile columns, the colloid was mobile (collision efficiencies from 0.05 to 0.08) both after the presence of Na(+) and Ca(2+) ions followed by deionised water influent. In the biofilm-grown column, the same treatment did not result in colloid retention in the case of Na(+) exposure, but in altered or enhanced colloid transport. In the case of Ca(2+) ions exposure, colloid retention increased with biofilm age. After 3 weeks, almost complete retention was observed. Similar observations were made in columns packed with material from slow sand filtration units. These data reveal the complex interactions between biofilms, cations and colloid transport. Changes in the electrolyte composition of water percolating the subsurface can frequently occur and will result in different colloid transport characteristics with regard to the dominating species of ions and the relative abundance of microbial biofilms. This has to be considered when modelling colloid transport through the subsurface.

  9. Transport of Intrinsic Plutonium Colloids in Saturated Porous Media

    NASA Astrophysics Data System (ADS)

    Zhou, D.; Abdel-Fattah, A.; Boukhalfa, H.; Ware, S. D.; Tarimala, S.; Keller, A. A.

    2011-12-01

    Actinide contaminants were introduced to the subsurface environment as a result of nuclear weapons development and testing, as well as for nuclear power generation and related research activities for defense and civilian applications. Even though most actinide species were believed to be fairly immobile once in the subsurface, recent studies have shown the transport of actinides kilometers away from their disposal sites. For example, the treated liquid wastes released into Mortandad Canyon at the Los Alamos National Laboratory were predicted to travel less than a few meters; however, plutonium and americium have been detected 3.4 km away from the waste outfall. A colloid-facilitated mechanism has been suggested to account for this unexpected transport of these radioactive wastes. Clays, oxides, organic matters, and actinide hydroxides have all been proposed as the possible mobile phase. Pu ions associated with natural colloids are often referred to as pseudo-Pu colloids, in contrast with the intrinsic Pu colloids that consist of Pu oxides. Significant efforts have been made to investigate the role of pseudo-Pu colloids, while few studies have evaluated the environmental behavior of the intrinsic Pu colloids. Given the fact that Pu (IV) has extremely low solubility product constant, it can be inferred that the transport of Pu in the intrinsic form is highly likely at suitable environmental conditions. This study investigates the transport of intrinsic Pu colloids in a saturated alluvium material packed in a cylindrical column (2.5-cm Dia. x 30-cm high) and compares the results to previous data on the transport of pseudo Pu colloids in the same material. A procedure to prepare a stable intrinsic Pu colloid suspension that produced consistent and reproducible electrokinetic and stability data was developed. Electrokinetic properties and aggregation stability were characterized. The Pu colloids, together with trillium as a conservative tracer, were injected into the

  10. General nonequilibrium theory of colloid dynamics.

    PubMed

    Ramírez-González, Pedro; Medina-Noyola, Magdaleno

    2010-12-01

    A nonequilibrium extension of Onsager's canonical theory of thermal fluctuations is employed to derive a self-consistent theory for the description of the statistical properties of the instantaneous local concentration profile n(r,t) of a colloidal liquid in terms of the coupled time-evolution equations of its mean value n(r,t) and of the covariance [Formula in text] of its fluctuations δn(r,t)=n(r,t)-n(r,t). These two coarse-grained equations involve a local mobility function b(r,t) which, in its turn, is written in terms of the memory function of the two-time correlation function [Formula in text]. For given effective interactions between colloidal particles and applied external fields, the resulting self-consistent theory is aimed at describing the evolution of a strongly correlated colloidal liquid from an initial state with arbitrary mean and covariance n(0)(r) and σ(0)(r,r') toward its equilibrium state characterized by the equilibrium local concentration profile n(eq)(r) and equilibrium covariance σ(eq)(r,r'). This theory also provides a general theoretical framework to describe irreversible processes associated with dynamic arrest transitions, such as aging, and the effects of spatial heterogeneities.

  11. 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.

  12. 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.

  13. Colloidal solitary waves with temperature dependent compressibility

    NASA Astrophysics Data System (ADS)

    Azmi, A.; Marchant, T. R.

    2014-05-01

    Spatial solitary waves which form in colloidal suspensions of dielectric nanoparticles are considered. The interactions, or compressibility, of the colloidal particles, is modelled using a series in the particle density, or packing fraction, where the virial, or series, coefficients depend on the type of particle interaction model. Both the theoretical hard disk and sphere repulsive models, and a model with temperature dependent compressibility, are considered. Experimental results show that particle interactions can be temperature dependent and either repulsive or attractive in nature, so we model the second virial coefficient using a physically realistic temperature power law. One- and two-dimensional semi-analytical colloidal solitary wave solutions are found. Trial functions, based on the form of the nonlinear Schrödinger equation soliton, are used, together with averaging, to develop the semi-analytical solutions. When the background packing fraction is low, the one-dimensional solitary waves have three solutions branches (with a bistable regime) while the two-dimensional solitary waves have two solution branches, with a single stable branch. The temperature dependent second virial coefficient results in changes to the solitary wave properties and the parameter space, in which multiple solutions branches occur. An excellent comparison is found between the semi-analytical and numerical solutions.

  14. Colloidal competences of any polyethyleneglycol conjugates.

    PubMed

    Jianu, C; Cocan, Ileana; Rujescu, Cristina; Jianu, I

    2008-01-01

    The present paper presents research rely on the knowledge of basic colloidal competences (surface tension, critical micelar concentration, HLB value) of certain new structured lipids by accessing "homogeneous" polyoxyethylene chains (n=3-18) (PEGn) monoderivatized R(NF; EH) during processing by cyanoethylation, hydrolysis, and esterification together with fatty acids (R') isolated and characterized from grape seeds (Vitis vinifera) (S), wild chestnut (Aesculus hyppocastanum) (Ca), wild rose (Rosa Canina) (mn), coriander (Coriandri fructus) (Co) in the architecture of the conjugates about foaming and wetting competences. Basic colloidal characterisation aimed at directing future research to optimagrape seed technological directions for agroalimentary and horticultural processing (and not only) among which these structures through synergic cumulus of defining competences of the polyunsaturated fatty acids (1 delta; 2delta; 3delta), of "homogeneous" derivatised polyethyleneoxy chains (PEO) with monitored degree of oligomerization (n=3-18). We thought it useful to access oligomeric chains PEO processed through adapted Williamson synthesis to clearly quantify its role in the global "colloidal fingerprint" of the studied conjugate. On the other hand, polyunsaturated plant lipid residues we selected constitute a variant of valorification by-products from horticultural and/or agroalimentary processing accessible over worldwide geographical areas with differences due to soil and climate conditions and to the cultivars specific to spontaneous and cultivated flora.

  15. Patchy polymer colloids with tunable anisotropy dimensions.

    PubMed

    Kraft, Daniela J; Hilhorst, Jan; Heinen, Maria A P; Hoogenraad, Mathijs J; Luigjes, Bob; Kegel, Willem K

    2011-06-09

    We present the synthesis of polymer colloids with continuously tunable anisotropy dimensions: patchiness, roughness, and branching. Our method makes use of controlled fusion of multiple protrusions on highly cross-linked polymer particles produced by seeded emulsion polymerization. Carefully changing the synthesis conditions, we can tune the number of protrusions, or branching, of the obtained particles from spheres with one to three patches to raspberry-like particles with multiple protrusions. In addition to that, roughness is generated on the seed particles by adsorption of secondary nucleated particles during synthesis. The size of the roughness relative to the smooth patches can be continuously tuned by the initiator, surfactant, and styrene concentrations. Seed colloids chemically different from the protrusions induce patches of different chemical nature. The underlying generality of the synthesis procedure allows for application to a variety of seed particle sizes and materials. We demonstrate the use of differently sized polyNIPAM (poly-N-isopropylacrylamide), as well as polystyrene and magnetite filled polyNIPAM seed particles, the latter giving rise to magnetically anisotropic colloids. The high yield together with the uniform, anisotropic shape make them interesting candidates for use as smart building blocks in self-assembling systems.

  16. 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

  17. 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

  18. Improving feed slurry rheology by colloidal techniques

    SciTech Connect

    Heath, W.O.; Ternes, R.L.

    1984-06-01

    Pacific Northwest Laboratory (PSN) has investigated three colloidal techniques in the laboratory to improve the sedimentation and flowability of Hanford simulated (nonradioactive) current acid waste (CAW) melter feed slurry: polymer-induced bridging flocculation; manipulating glass former (raw SiO/sub 2/ or frit) particle size; and alteration of nitric acid content. All three methods proved successful in improving the rheology of the simulated CAW feed. This initially had exhibited nearly worst-case flow and clogging properties, but was transformed into a flowable, resuspendable (nonclogging) feed. While each has advantages and disadvantages, the following three specific alternatives proved successful: addition of a polyelectrolyte in 2000 ppM concentration to feed slurry; substitution of a 49 wt % SiO/sub 2/ colloidal suspension (approx. 10-micron particle size) for the -325 mesh (less than or equal to 44-micron particle size) raw-chemical SiO/sub 2/; and increase of nitric acid content from the reference 1.06 M to optimum 1.35 M. The first method, polymer-induced bridging flocculation, results in a high sediment volume, nonclogging CAW feed. The second method, involving the use of colloidal silica particles results in a nonsedimenting feed that when left unagitated forms a gel. The third method, increase in feed acidity, results in a highly resuspendable (nonclogging) melter feed. Further research is therefore required to determine which of the three alternatives is the preferred method of achieving rheological control of CAW melter feeds.

  19. 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.

  20. Dissipative Particle Dynamics simulation of colloidal suspensions

    NASA Astrophysics Data System (ADS)

    Jamali, Safa; Boromand, Arman; Maia, Joao

    2014-03-01

    DPD as a mesoscale method was firstly proposed to study dynamics of suspensions under flow condition. However the proposed method failed to capture shear properties of suspensions because it lacked: first a potential to reproduce lubrication forces and second a clear definition for the colloid surface. Recently we reported a modified DPD method which defines colloidal particles as particles with hard core and a dissipative coat. An additional lubrication force was introduced to include the short-range hydrodynamics that are not captured in original DPD. The model was found to be able to reproduce shear properties of suspensions for a wide range of different systems, from monodisperse to bimodal with different volume fractions, compositions and size ratios. In present work our modified DPD method is employed to study both equilibrium and flow properties of colloidal suspension. Zero shear viscosity of suspension is measured using Green-Kubo expressions and the results are compared to theoretical predictions. Furthermore, structure formation in suspensions is studied in respect to energy landscape of the fluid both at rest and under flow.

  1. 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).

  2. Local elastic response measured near the colloidal glass transition

    NASA Astrophysics Data System (ADS)

    Anderson, D.; Schaar, D.; Hentschel, H. G. E.; Hay, J.; Habdas, Piotr; Weeks, Eric R.

    2013-03-01

    We examine the response of a dense colloidal suspension to a local force applied by a small magnetic bead. For small forces, we find a linear relationship between the force and the displacement, suggesting the medium is elastic, even though our colloidal samples macroscopically behave as fluids. We interpret this as a measure of the strength of colloidal caging, reflecting the proximity of the samples' volume fractions to the colloidal glass transition. The strain field of the colloidal particles surrounding the magnetic probe appears similar to that of an isotropic homogeneous elastic medium. When the applied force is removed, the strain relaxes as a stretched exponential in time. We introduce a model that suggests this behavior is due to the diffusive relaxation of strain in the colloidal sample.

  3. Self-pinning by colloids confined at a contact line

    NASA Astrophysics Data System (ADS)

    Weon, Byung; Je, Jung

    2013-03-01

    Colloidal particles suspended in a fluid usually inhibit complete wetting of the fluid on a solid surface and cause pinning of the contact line, known as self-pinning. We show differences in spreading and drying behaviors of pure and colloidal droplets using optical and confocal imaging methods. These differences come from spreading inhibition by colloids confined at a contact line. We propose a self-pinning mechanism based on spreading inhibition by colloids. We find a good agreement between the mechanism and the experimental result taken by directly tracking individual colloids near the contact lines of evaporating colloidal droplets. This research was supported by the Creative Research Initiatives (Functional X-ray Imaging) of MEST/NRF.

  4. Evanescent wave excited luminescence from levitated quantum dot modified colloids.

    PubMed

    Everett, W Neil; Beckham, Richard E; Meissner, Kenith; Bevan, Michael A

    2007-08-14

    Evanescent wave excited luminescence of quantum dot modified polystyrene (QDPS) colloids is investigated to measure potential energy profiles of QDPS colloids electrostatically levitated above a planar glass surface. Luminescence is characterized for three different-sized PS colloids modified with three different-sized QDs using confocal microscopy, emission spectra, flow cytometry, and temporal measurements of levitated and deposited colloids. Colloid-surface potential energy profiles constructed from scattering and luminescence intensity data display excellent agreement with each other, theoretical predictions, and independently measured parameters. QDPS luminescence intensity is indirectly confirmed to have an exponential dependence on height similar to conventional colloidal evanescent wave scattering. Our findings indicate that evanescent wave excited QDPS luminescence could enable total internal reflection microscopy measurements of index-matched hard spheres, multiple specific biomolecular interactions via spectral multiplexing, enhanced morphology-dependent resonance modes, and integrated evanescent wave-video-confocal microscopy experiments not possible with scattering.

  5. Inertial and viscoelastic forces on rigid colloids in microfluidic channels.

    PubMed

    Howard, Michael P; Panagiotopoulos, Athanassios Z; Nikoubashman, Arash

    2015-06-14

    We perform hybrid molecular dynamics simulations to study the flow behavior of rigid colloids dispersed in a dilute polymer solution. The underlying Newtonian solvent and the ensuing hydrodynamic interactions are incorporated through multiparticle collision dynamics, while the constituent polymers are modeled as bead-spring chains, maintaining a description consistent with the colloidal nature of our system. We study the cross-stream migration of the solute particles in slit-like channels for various polymer lengths and colloid sizes and find a distinct focusing onto the channel center under specific solvent and flow conditions. To better understand this phenomenon, we systematically measure the effective forces exerted on the colloids. We find that the migration originates from a competition between viscoelastic forces from the polymer solution and hydrodynamically induced inertial forces. Our simulations reveal a significantly stronger fluctuation of the lateral colloid position than expected from thermal motion alone, which originates from the complex interplay between the colloid and polymer chains.

  6. 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.

  7. Defect Dynamics and Zipping of 2D Colloidal Crystallites

    NASA Astrophysics Data System (ADS)

    Bowley, Chris; Smullin, Sylvia; Ling, Xinsheng

    1998-03-01

    We use video microscopy to study defect dynamics in 2D colloidal (charged polystyrene microspheres) crystallites formed at the water-air interface. For small 2D crystallites, one might expect to see free edge dislocations in such small systems since the cost of forming such defects scales logarithmically with the size of the crystallite. But we found that as soon as an edge dislocation forms, it quickly moves to the edge of the crystallite and disappears. This is due to an attraction with an image dislocation outside the edge. As a result, most crystallites are defect-free during most of the time. Interesting things happen when two crystallites try to bind to each other, or zip together. A sharp transition occurs at the shared edge of the two crystallites during the zipping process. This is clearly manifested by a sudden change in the relative velocity between two drifting crystallites or a sudden re-orientation of one of the crystallites relative to the other. This work was supported by the startup funds and a Richard Salomon Faculty Research Award from Brown University.

  8. Modifying Thermal Transport in Colloidal Nanocrystal Solids with Surface Chemistry.

    PubMed

    Liu, Minglu; Ma, Yuanyu; Wang, Robert Y

    2015-12-22

    We present a systematic study on the effect of surface chemistry on thermal transport in colloidal nanocrystal (NC) solids. Using PbS NCs as a model system, we vary ligand binding group (thiol, amine, and atomic halides), ligand length (ethanedithiol, butanedithiol, hexanedithiol, and octanedithiol), and NC diameter (3.3-8.2 nm). Our experiments reveal several findings: (i) The ligand choice can vary the NC solid thermal conductivity by up to a factor of 2.5. (ii) The ligand binding strength to the NC core does not significantly impact thermal conductivity. (iii) Reducing the ligand length can decrease the interparticle distance, which increases thermal conductivity. (iv) Increasing the NC diameter increases thermal conductivity. (v) The effect of surface chemistry can exceed the effect of NC diameter and becomes more pronounced as NC diameter decreases. By combining these trends, we demonstrate that the thermal conductivity of NC solids can be varied by an overall factor of 4, from ∼0.1-0.4 W/m-K. We complement these findings with effective medium approximation modeling and identify thermal transport in the ligand matrix as the rate-limiter for thermal transport. By combining these modeling results with our experimental observations, we conclude that future efforts to increase thermal conductivity in NC solids should focus on the ligand-ligand interface between neighboring NCs.

  9. Colloidal Surfaces with Boundaries, Apex Boojums, and Nested Elastic Self-Assembly of Nematic Colloids

    NASA Astrophysics Data System (ADS)

    Park, Sungoh; Liu, Qingkun; Smalyukh, Ivan I.

    2016-12-01

    Self-assembly of colloidal particles is poised to become a powerful composite material fabrication technique, but remains challenged by a limited control over the ensuing structures. We develop a new breed of nematic colloids that are physical analogs of a mathematical surface with boundary, interacting with the molecular alignment field without inducing defects when flat. However, made from a thin nanofoil, they can be shaped to prompt formation of self-compensating defects that drive preprogramed elastic interactions mediated by the nematic host. To show this, we wrap the nanofoil on all triangular side faces of a pyramid, except its square base. The ensuing pyramidal cones induce point defects with fractional hedgehog charges of opposite signs, spontaneously align with respect to the far-field director to form elastic dipoles and nested assemblies with tunable spacing. Nanofoils shaped into octahedrons interact as elastic quadrupoles. Our findings may drive realization of low-symmetry colloidal phases.

  10. [Bactericidal activity of colloidal silver against grampositive and gramnegative bacteria].

    PubMed

    Afonina, I A; Kraeva, L A; Tseneva, G Ia

    2010-01-01

    It was shown that colloidal silver solution prepared in cooperation with the A. F. Ioffe Physical Technical Institute of the Russian Academy of Sciences, had significant bactericidal activity. Stable bactericidal effect on gramnegative microorganisms was observed after their 2-hour exposition in the solution of colloidal silver at a concentration of 10 ppm. Grampositive capsule-forming microorganisms were less susceptible to the colloidal silver solution: their death was observed after the 4-hour exposition in the solution.

  11. Influence of Nanoscale Surface Roughness on Colloidal Force Measurements.

    PubMed

    Zou, Yi; Jayasuriya, Sunil; Manke, Charles W; Mao, Guangzhao

    2015-09-29

    Forces between colloidal particles determine the performances of many industrial processes and products. Colloidal force measurements conducted between a colloidal particle AFM probe and particles immobilized on a flat substrate are valuable in selecting appropriate surfactants for colloidal stabilization. One of the features of inorganic fillers and extenders is the prevalence of rough surfaces-even the polymer latex particles, often used as model colloidal systems including the current study, have rough surfaces albeit at a much smaller scale. Surface roughness is frequently cited as the reason for disparity between experimental observations and theoretical treatment but seldom verified by direct evidence. This work reports the effect of nanoscale surface roughness on colloidal force measurements carried out in the presence of surfactants. We applied a heating method to reduce the mean surface roughness of commercial latex particles from 30 to 1 nm. We conducted force measurements using the two types of particles at various salt and surfactant concentrations. The surfactants used were pentaethylene glycol monododecyl ether, Pluronic F108, and a styrene/acrylic copolymer, Joncryl 60. In the absence of the surfactant, nanometer surface roughness affects colloidal forces only in high salt conditions when the Debye length becomes smaller than the surface roughness. The adhesion is stronger between colloids with higher surface roughness and requires a higher surfactant concentration to be eliminated. The effect of surface roughness on colloidal forces was also investigated as a function of the adsorbed surfactant layer structure characterized by AFM indentation and dynamic light scattering. We found that when the layer thickness exceeds the surface roughness, the colloidal adhesion is less influenced by surfactant concentration variation. This study demonstrates that surface roughness at the nanoscale can influence colloidal forces significantly and should be taken

  12. The Colloidal Stability of Magnetic Nanoparticles in Ionic Liquids

    DTIC Science & Technology

    2014-09-01

    SEP 2014 2. REPORT TYPE Final 3. DATES COVERED 06-03-2013 to 05-06-2014 4. TITLE AND SUBTITLE The Colloidal Stability of Magnetic...DATES COVERED (From - To) 6 Mar 2013 – 5 June 2014 4. TITLE AND SUBTITLE The Colloidal Stability of Magnetic Nanoparticles in Ionic Liquids...Polymers and Colloids , Chemistry F11, The University of Sydney, NSW 2006, Australia. - Phone : +61 2 9351 6973 - Fax : +61 2 9351 851 Period of

  13. Computational Study of Colloidal Droplet Interactions with Three Dimensional Structures

    DTIC Science & Technology

    2015-05-18

    SECURITY CLASSIFICATION OF: The colloidal droplet spreading on and sorption into a porous medium is important to 3D printing technology. In this study... colloidal fluid distribution in the porous structure after sorption of single/multiple droplets in powder beds. The spreading of the droplet on the surface...Feb-2015 Approved for Public Release; Distribution Unlimited Final Report: Computational Study of Colloidal Droplet Interactions with Three Dimensional

  14. Exotic crystal superstructures of colloidal crystals in confinement.

    PubMed

    Fontecha, Ana Barreira; Schöpe, Hans Joachim

    2008-06-01

    Colloidal model systems have been used for over three decades for investigating liquids, crystals, and glasses. Colloidal crystal superstructures have been observed in binary systems of repulsive spheres as well as oppositely charged sphere systems showing structures well known from atomic solids. In this work we study the structural transition of colloidal crystals under confinement. In addition to the known sequence of crystalline structures, crystal superstructures with dodecagonal and hexagonal symmetry are observed in one component systems. These structures have no atomic counterpart.

  15. Colloidal crystallization of colloidal silica grafted with iron(0) complex-tethered polymers in organic solvents

    NASA Astrophysics Data System (ADS)

    Yoshinaga, Kohji; Mouri, Emiko

    2007-09-01

    Incorporation of iron(0) complex into polymer-grafted silica and colloidal crystallization in organic solvent were studied. In this study, zero-valence iron complex, vinylferrocene (Vfc) and iron(0)tricarbonyl(4,4-dimethyl-1,-4-cyclohexadienyl) acrylate (Fe(0)Ac) or methacrylate (Fe(0)Me), were introduced into grafted polymer to prevent from increasing ionic strength in colloidal crystallization system. Poly(methyl methacrylate (MMA)-co-Vfc)-grafted silica never formed colloidal crystals in polar solvent, such as acetone or acetonitrile. However, increasing ferrocenyl group fraction in the polymer resulted in disturbing the crystallization. Poly(N-isopropylacrylamide (NIPAAm)-co-Vfc)-grafted silica, which was composed of mole fraction of Vfc, 1/3, afforded crystallization in ethanol over the particle fraction of 0.053. In the case of diene-Fe(0)(CO) 3/polymer-grafted silica, poly(MMA-co-Fe(0)Ac)-, poly(NIPAAm-co-Fe(0)Ac)- and poly(N.N-dimethylacrylamide (DMAAm)-co-Fe(0)Ac)-grafted silica gave colloidal crystallization in relatively low polar solvents, DMF, acetone, acetonirile and ethanol, critical volume fraction for which were in the range from 0.054 to 0.117. In the case of copolymer-grafted silica containing Fe(0)Me, poly(MMA-co-FeMe)-grafted silica crystallized in DMF, Interestingly, especially in cases of polymer-grafted silica containing Fe(0)Ac or Fe(0)Me composed of the highest mole fraction Fe(0)Me, 1/2, afforded crystallization in DMF. The iridescence color of the colloidal crystals was changed with the combination of grafted polymer and solvent. The characteristic coloration of the solution from reddish to greenish color is possibly due to absorption of blue light region by diene-Fe(0)(CO) 3 complex and Bragg deflection on colloidal crystals.

  16. Nanoimprint-Transfer-Patterned Solids Enhance Light Absorption in Colloidal Quantum Dot Solar Cells.

    PubMed

    Kim, Younghoon; Bicanic, Kristopher; Tan, Hairen; Ouellette, Olivier; Sutherland, Brandon R; García de Arquer, F Pelayo; Jo, Jea Woong; Liu, Mengxia; Sun, Bin; Liu, Min; Hoogland, Sjoerd; Sargent, Edward H

    2017-04-12

    Colloidal quantum dot (CQD) materials are of interest in thin-film solar cells due to their size-tunable bandgap and low-cost solution-processing. However, CQD solar cells suffer from inefficient charge extraction over the film thicknesses required for complete absorption of solar light. Here we show a new strategy to enhance light absorption in CQD solar cells by nanostructuring the CQD film itself at the back interface. We use two-dimensional finite-difference time-domain (FDTD) simulations to study quantitatively the light absorption enhancement in nanostructured back interfaces in CQD solar cells. We implement this experimentally by demonstrating a nanoimprint-transfer-patterning (NTP) process for the fabrication of nanostructured CQD solids with highly ordered patterns. We show that this approach enables a boost in the power conversion efficiency in CQD solar cells primarily due to an increase in short-circuit current density as a result of enhanced absorption through light-trapping.

  17. Test of the Universal Scaling Law of Diffusion in Colloidal Monolayers

    NASA Astrophysics Data System (ADS)

    Ma, Xiaoguang; Chen, Wei; Wang, Ziren; Peng, Yuan; Han, Yilong; Tong, Penger

    2013-02-01

    Using the techniques of optical microscopy and particle tracking, we measure the pair correlation function and Brownian diffusion in monolayers of strongly interacting colloidal particles suspended at or near three different interfaces and test the universal scaling law of the normalized diffusion coefficient, D˜≃eαΔS, as a function of the excess entropy ΔS for a wide range of particle concentrations. It is found that the universal scaling law with α=1 holds well for highly charged polystyrene spheres suspended at an air-water interface, where the strong electrostatic interactions play a dominant role. For monolayer suspensions of hard-sphere-like particles, where hydrodynamic interactions become important, deviations from the universal scaling law are observed. The experiment indicates that the hydrodynamic corrections could be incorporated into the universal scaling law of diffusion with an exponent α<1.

  18. 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.

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

    PubMed

    Fu, Huiying; Tsang, Sai-Wing

    2012-04-07

    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.

  20. Nonlinear Optical Properties of Colloids with Carbon Nanoparticles

    NASA Astrophysics Data System (ADS)

    Mayor, A. Yu.; Proschenko, D. Yu.; Golik, S. S.; Postnova, I. V.; Shchipunov, Yu. A.; Podlesnyh, A. A.

    Experimentally studied linear and nonlinear characteristics of colloid on the basis of a new class of carbon nanoparticles (CN) synthesized by hydrothermal synthesis. The spectral characteristics of supercontinuum of the colloids with CN in the range 420 - 700 nm were investigated. The effectiveness of excitation of one- and two-photon fluorescence colloids with UN was determined. The anomalous dependence of the nonlinear refractive index of the wavelength of the radiation was revealed. It was installed that the efficiency of spectral transformation of the supercontinuum process in the case of colloid with carbon nanoparticles is less in the anti-stokes region than in case with water.

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. Size and density of a /sup 242/Pu colloid

    SciTech Connect

    Rundberg, R.S.; Mitchell, A.J.; Torstenfelt, N.B.

    1987-01-01

    The size and density of a /sup 242/Pu colloid has been measured by autocorrelation photon spectrometry. The density of the colloid was determined by ultraspeed centrifugation. From the concentration profiles of /sup 242/Pu in the centrifuged test tubes, a standard sedimentation formula was used to calculate the density; the size of the colloid was known from the light scattering experiments. The determined density of the /sup 242/Pu colloid was unexpectedly low compared to the density of crystalline PuO/sub 2/. 5 refs., 1 tab.

  6. Modes of surface premelting in colloidal crystals composed of attractive particles

    NASA Astrophysics Data System (ADS)

    Li, Bo; Wang, Feng; Zhou, Di; Peng, Yi; Ni, Ran; Han, Yilong

    2016-03-01

    Crystal surfaces typically melt into a thin liquid layer at temperatures slightly below the melting point of the crystal. Such surface premelting is prevalent in all classes of solids and is important in a variety of metallurgical, geological and meteorological phenomena. Premelting has been studied using X-ray diffraction and differential scanning calorimetry, but the lack of single-particle resolution makes it hard to elucidate the underlying mechanisms. Colloids are good model systems for studying phase transitions because the thermal motions of individual micrometre-sized particles can be tracked directly using optical microscopy. Here we use colloidal spheres with tunable attractions to form equilibrium crystal-vapour interfaces, and study their surface premelting behaviour at the single-particle level. We find that monolayer colloidal crystals exhibit incomplete premelting at their perimeter, with a constant liquid-layer thickness. In contrast, two- and three-layer crystals exhibit conventional complete melting, with the thickness of the surface liquid diverging as the melting point is approached. The microstructures of the surface liquids differ in certain aspects from what would be predicted by conventional premelting theories. Incomplete premelting in the monolayer crystals is triggered by a bulk isostructural solid-solid transition and truncated by a mechanical instability that separately induces homogeneous melting within the bulk. This finding is in contrast to the conventional assumption that two-dimensional crystals melt heterogeneously from their free surfaces (that is, at the solid-vapour interface). The unexpected bulk melting that we observe for the monolayer crystals is accompanied by the formation of grain boundaries, which supports a previously proposed grain-boundary-mediated two-dimensional melting theory. The observed interplay between surface premelting, bulk melting and solid-solid transitions challenges existing theories of surface

  7. Modes of surface premelting in colloidal crystals composed of attractive particles.

    PubMed

    Li, Bo; Wang, Feng; Zhou, Di; Peng, Yi; Ni, Ran; Han, Yilong

    2016-03-24

    Crystal surfaces typically melt into a thin liquid layer at temperatures slightly below the melting point of the crystal. Such surface premelting is prevalent in all classes of solids and is important in a variety of metallurgical, geological and meteorological phenomena. Premelting has been studied using X-ray diffraction and differential scanning calorimetry, but the lack of single-particle resolution makes it hard to elucidate the underlying mechanisms. Colloids are good model systems for studying phase transitions because the thermal motions of individual micrometre-sized particles can be tracked directly using optical microscopy. Here we use colloidal spheres with tunable attractions to form equilibrium crystal-vapour interfaces, and study their surface premelting behaviour at the single-particle level. We find that monolayer colloidal crystals exhibit incomplete premelting at their perimeter, with a constant liquid-layer thickness. In contrast, two- and three-layer crystals exhibit conventional complete melting, with the thickness of the surface liquid diverging as the melting point is approached. The microstructures of the surface liquids differ in certain aspects from what would be predicted by conventional premelting theories. Incomplete premelting in the monolayer crystals is triggered by a bulk isostructural solid-solid transition and truncated by a mechanical instability that separately induces homogeneous melting within the bulk. This finding is in contrast to the conventional assumption that two-dimensional crystals melt heterogeneously from their free surfaces (that is, at the solid-vapour interface). The unexpected bulk melting that we observe for the monolayer crystals is accompanied by the formation of grain boundaries, which supports a previously proposed grain-boundary-mediated two-dimensional melting theory. The observed interplay between surface premelting, bulk melting and solid-solid transitions challenges existing theories of surface

  8. Crystal nuclei in melts: a Monte Carlo simulation of a model for attractive colloids

    NASA Astrophysics Data System (ADS)

    Statt, Antonia; Virnau, Peter; Binder, Kurt

    2015-09-01

    As a model for a suspension of hard-sphere-like colloidal particles where small non-adsorbing dissolved polymers create a depletion attraction, we introduce an effective colloid-colloid potential closely related to the Asakura-Oosawa model, but that does not have any discontinuities. In simulations, this model straightforwardly allows the calculation of the pressure from the virial formula, and the phase transition in the bulk from the liquid to crystalline solid can be accurately located from a study where a stable coexistence of a crystalline slab with a surrounding liquid phase occurs. For this model, crystalline nuclei surrounded by fluid are studied both by identifying the crystal-fluid interface on the particle level (using suitable bond orientational order parameters to distinguish the phases) and by 'thermodynamic' means, i.e. the latter method amounts to compute the enhancement of chemical potential and pressure relative to their coexistence values. We show that the chemical potential can be obtained from simulating thick films, where one wall with a rather long-range repulsion is present, since near this wall, the Widom particle insertion method works, exploiting the fact that the chemical potential in the system is homogeneous. Finally, the surface excess free energy of the nucleus is obtained, for a wide range of nuclei volumes. From this method, it is established that classical nucleation theory works, showing that for the present model, the anisotropy of the interface excess free energy of crystals and their resulting non-spherical shape has only a very small effect on the barrier.

  9. Colloidal interactions between Langmuir-Blodgett bitumen films and fine solid particles.

    PubMed

    Long, Jun; Zhang, Liyan; Xu, Zhenghe; Masliyah, Jacob H

    2006-10-10

    In oil sand processing, accumulation of surface-active compounds at various interfaces imposes a significant impact on bitumen recovery and bitumen froth cleaning (i.e., froth treatment) by altering the interfacial properties and colloidal interactions among various oil sand components. In the present study, bitumen films were prepared at toluene/water interfaces using a Langmuir-Blodgett (LB) upstroke deposition technique. The surface of the prepared LB bitumen films was found to be hydrophobic, comprised of wormlike aggregates containing a relatively high content of oxygen, sulfur, and nitrogen, indicating an accumulation of surface-active compounds in the films. Using an atomic force microscope, colloidal interactions between the LB bitumen films and fine solids (model silica particles and clay particles chosen directly from an oil sand tailing stream) were measured in industrial plant process water and compared with those measured in simple electrolyte solutions of controlled pH and divalent cation concentrations. The results show a stronger long-range repulsive force and weaker adhesion force in solutions of higher pH and lower divalent cation concentration. In plant process water, a moderate long-range repulsive force and weak adhesion were measured despite its high electrolyte content. These findings provide more insight into the mechanisms of bitumen extraction and froth treatment.

  10. Identification of Al13 on the Colloid Surface Using Surface-Enhanced Raman Spectroscopy.

    PubMed

    Li, Ning; Hu, Chengzhi; Fu, Xiaoning; Xu, Xiufang; Liu, Rui; Liu, Huijuan; Qu, Jiuhui

    2017-02-21

    Al13 is the most active polymeric Al species responsible for coagulation at the solid-liquid interface, whereas the detection techniques for Al13 at the interface are currently limited. In this study, for the first time, the identification of Al13 on the silicon dioxide-based colloid surface was realized by using surface-enhanced Raman scattering (SERS), which is an ideal surface method sensitive for single-molecule detection. The high purity Al13 salts were prepared by an electrolysis procedure followed by precipitation or metathesis. Al13-Cln was determined to be feasible for the Raman detection as it exhibited more noticeable signals in comparison to Al13-(SO4)p and Al13-(NO3)m. The peak of Al13-Cln at 635 cm(-1) could be the major characteristic peak of Al13, and the other two peaks at 300 and 987 cm(-1) could be accessorial evidence for the identification. Further, the identification of Al13 adsorbed on the surface of Ag and gold-core/silica-shell colloids was confirmed by the SERS response at the above three wavenumbers with a higher signal-to-noise ratio than the normal Raman scattering. According to the least-squares fitting computed Raman spectra, each of the characteristic peaks was associated with specific vibrational modes.

  11. Controlling the complexation of polysaccharides into multi-functional colloidal assemblies for nanomedicine.

    PubMed

    Costalat, M; Alcouffe, P; David, L; Delair, T

    2014-09-15

    The controlled assembly of oppositely charged polysaccharides led to colloids stable in physiological media, capable of encapsulating a molecular drug and of sorbing proteins at their interface. Two types of particles were obtained: both chitosan-dextran sulfate (CS-DS) and chitosan-heparin (CS-HP) stable over 30 days in PBS at 25 and 37°C. At gastric pH 1.2, these particles remained stable over 3 days, enough for a stomach transit. The structural analysis by small angle X-ray scattering (SAXS) showed that CS-DS surface was semi-rough and chains inside particle exhibited rod-like conformation. Moreover, the particle interfaces could efficiently be functionalized with anti-OVA or anti-α4β7 antibodies, in PBS, with the conservation of the antibody bioactivity over at least 8 days. Finally, during the assembly process, a molecular model drug, AMP, could be encapsulated with a loading efficiency up to 72% for CS-DS particles and 66% for CS-HP. All these data establish that the controlled assembly process under equilibrium conditions lead to colloids well suited for the targeted nanodelivery of drugs.

  12. 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

  13. 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.

  14. Ionic Structure at Dielectric Interfaces

    NASA Astrophysics Data System (ADS)

    Jing, Yufei

    The behavior of ions in liquids confined between macromolecules determines the outcome of many nanoscale assembly processes in synthetic and biological materials such as colloidal dispersions, emulsions, hydrogels, DNA, cell membranes, and proteins. Theoretically, the macromolecule-liquid boundary is often modeled as a dielectric interface and an important quantity of interest is the ionic structure in a liquid confined between two such interfaces. The knowledge gleaned from the study of ionic structure in such models can be useful in several industrial applications, such as biosensors, lithium-ion batteries double-layer supercapacitors for energy storage and seawater desalination. Electrostatics plays a critical role in the development of such functional materials. Many of the functions of these materials, result from charge and composition heterogeneities. There are great challenges in solving electrostatics problems in heterogeneous media with arbitrary shapes because electrostatic interactions remains unknown but depend on the particular density of charge distributions. Charged molecules in heterogeneous media affect the media's dielectric response and hence the interaction between the charges is unknown since it depends on the media and on the geometrical properties of the interfaces. To determine the properties of heterogeneous systems including crucial effects neglected in classical mean field models such as the hard core of the ions, the dielectric mismatch and interfaces with arbitrary shapes. The effect of hard core interactions accounts properly for short range interactions and the effect of local dielectric heterogeneities in the presence of ions and/or charged molecules for long-range interactions are both analyzed via an energy variational principle that enables to update charges and the medium's response in the same simulation time step. In particular, we compute the ionic structure in a model system of electrolyte confined by two planar dielectric

  15. Thermoelectricity and thermodiffusion in charged colloids.

    PubMed

    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

    2015-08-07

    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.

  16. Trion decay in colloidal quantum dots.

    PubMed

    Jha, Praket P; Guyot-Sionnest, Philippe

    2009-04-28

    Using charged films of colloidal CdSe/CdS core/shell quantum dots of approximately 3.5 to 4.5 nm core diameters and 0.6 to 1.2 nm thick CdS shells, the radiative and nonradiative decay of the negatively charged exciton, the trion T-, are measured. The T- radiative rate is faster than the exciton by a factor of 2.2 +/- 0.4 and estimated at approximately 10 ns. The T- lifetime is approximately 0.7-1.5 ns for the samples measured and is longer than the biexciton lifetime by a factor or 7.5 +/- 1.7.

  17. Argyria associated with colloidal silver supplementation.

    PubMed

    McKenna, Jeffrey K; Hull, Christopher M; Zone, John J

    2003-07-01

    A 65-year-old male presented for skin examination and was incidentally noted to have discoloration of the fingernails. These findings were completely asymptomatic. The patient had been taking colloidal silver supplementation (Silverzone 140 ppm silver Gifts of Nature, St. George, UT, USA) for 2 years as therapy for diabetes. He first noticed the onset of nail discoloration 1 year ago. His past medical history included type II diabetes and hypertension. His current medications were metformin, glyburide, and benazepril. Physical examination revealed slate-gray discoloration involving the lunulae of the fingernails (Fig. 1). The skin, mucous membranes, and sclerae were unaffected.

  18. 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.

  19. Colloidal polymeric nanoparticles and brain drug delivery.

    PubMed

    Khalil, Najeh Maissar; Mainardes, Rubiana Mara

    2009-07-01

    The blood brain barrier protects the brain from harmful substances in the blood stream and has stopped the development of many powerful and interesting drugs candidates for central nervous system due to the low poor distribution and by efflux mechanisms. Many different approaches have been developed in order to overcome this barrier and the drug gain access to the brain. The polymeric nanoparticles are efficient colloidal systems that have been investigated to the brain drug delivery. This review will focus on the current strategies for brain drug delivery emphasizing the properties and characteristics of polymeric nanoparticles for this purpose.

  20. 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