Characterization of Complex Colloidal Suspensions

Science.gov (United States)

Seaman, J. C.; Guerin, M.; Jackson, B. P.; Ranville, J. M.

2003-04-01

Surface chemical reactions play a major role in controlling contaminant fate and transport in the subsurface environment. Recent field and laboratory evidence suggests that mobile soil and groundwater colloids may facilitate the migration of sparingly soluble groundwater contaminants. Colloidal suspensions collected in the field or generated in laboratory column experiments tend to be fairly dilute in nature and comprised of relatively small particulates (reserved for studying ideal systems to the characterization of mobile colloids. However, many of these analytical techniques, including total/selective dissolution methods, dynamic light scattering, micro-electrophoresis, streaming potential, and even scanning electron microscopy (SEM), can be biased in of larger size fractions, and therefore, extremely sensitive to sampling, storage, and fractionation artifacts. In addition, surface modifiers such as sorbed oxides or organics can alter particulate appearance, composition, and behavior when compared to synthetic analogues or mineral standards. The current presentation will discuss the limitations and inherent biases associated with a number of analytical characterization techniques that are commonly applied to the study of mobile soil and groundwater colloids, including field flow fractionation (FFF) and acoustic based methods that have only recently become available.

Accelerated lattice Boltzmann model for colloidal suspensions rheology and interface morphology

CERN Document Server

Farhat, Hassan; Kondaraju, Sasidhar

2014-01-01

Colloids are ubiquitous in the food, medical, cosmetics, polymers, water purification, and pharmaceutical industries. The thermal, mechanical, and storage properties of colloids are highly dependent on their interface morphology and their rheological behavior. Numerical methods provide a convenient and reliable tool for the study of colloids. Accelerated Lattice Boltzmann Model for Colloidal Suspensions introduce the main building-blocks for an improved lattice Boltzmann–based numerical tool designed for the study of colloidal rheology and interface morphology. This book also covers the migrating multi-block used to simulate single component, multi-component, multiphase, and single component multiphase flows and their validation by experimental, numerical, and analytical solutions.   Among other topics discussed are the hybrid lattice Boltzmann method (LBM) for surfactant-covered droplets; biological suspensions such as blood; used in conjunction with the suppression of coalescence for investigating the...

Mesoscopic electrohydrodynamic simulations of binary colloidal suspensions

NARCIS (Netherlands)

Rivas, Nicolas; Frijters, Stefan; Pagonabarraga, Ignacio; Harting, Jens

2018-01-01

A model is presented for the solution of electrokinetic phenomena of colloidal suspensions in fluid mixtures. We solve the discrete Boltzmann equation with a Bhatnagar-Gross-Krook collision operator using the lattice Boltzmann method to simulate binary fluid flows. Solvent-solvent and solvent-solute

Emergent structures and dynamics in suspensions of self-phoretic colloids

Science.gov (United States)

Scagliarini, Andrea; Pagonabarraga, Ignacio

2013-11-01

Active fluids, such as suspensions of self-propelled particles , are a fascinating example of Soft Matter displaying complex collective behaviours which provide challenges in non-equilibrium Statistical Physics. The recent development of techniques to assemble miniaturized devices has led to a growing interest for micro and nanoscale engines that can perform autonomous motion (``microrobots''), as, for instance, self-phoretic colloids, for which the propulsion is induced by the generation of a chemical species in a reaction catalyzed at the particle surface. We perform a mesoscopic numerical study of suspensions of self-phoretic colloids. We show that, at changing the sign of the phoretic mobility (which accounts for the colloid-solute interactions), the system switches from a cluster phase to a state with slowed dynamics. We find that the cluster size distribution follows an exponential behaviour, with a characteristic size growing linearly with the colloid activity, while the density fluctuations grow as a power-law with an exponent depending on the cluster fractal dimension.We single out hydrodynamic interactions, showing that their effect is to work against cluster formation. For positive μ, we observe that colloids tend to reach an ordered state on a triangular lattice.

DC electrophoresis and viscosity of realistic salt-free concentrated suspensions: non-equilibrium dissociation-association processes.

Science.gov (United States)

Ruiz-Reina, Emilio; Carrique, Félix; Lechuga, Luis

2014-03-01

Most of the suspensions usually found in industrial applications are concentrated, aqueous and in contact with the atmospheric CO2. The case of suspensions with a high concentration of added salt is relatively well understood and has been considered in many studies. In this work we are concerned with the case of concentrated suspensions that have no ions different than: (1) those stemming from the charged colloidal particles (the added counterions, that counterbalance their surface charge); (2) the H(+) and OH(-) ions from water dissociation, and (3) the ions generated by the atmospheric CO2 contamination. We call this kind of systems "realistic salt-free suspensions". We show some theoretical results about the electrophoretic mobility of a colloidal particle and the electroviscous effect of realistic salt-free concentrated suspensions. The theoretical framework is based on a cell model that accounts for particle-particle interactions in concentrated suspensions, which has been successfully applied to many different phenomena in concentrated suspensions. On the other hand, the water dissociation and CO2 contamination can be described following two different levels of approximation: (a) by local equilibrium mass-action equations, because it is supposed that the reactions are so fast that chemical equilibrium is attained everywhere in the suspension, or (b) by non-equilibrium dissociation-association kinetic equations, because it is considered that some reactions are not rapid enough to ensure local chemical equilibrium. Both approaches give rise to different results in the range from dilute to semidilute suspensions, causing possible discrepancies when comparing standard theories and experiments concerning transport properties of realistic salt-free suspensions. Copyright © 2013 Elsevier Inc. All rights reserved.

Active and Nonlinear Microrheology of Dense Colloidal Suspensions

OpenAIRE

Harrer, Christian Josef

2013-01-01

In this work, we have investigated active and nonlinear microrheology of dense colloidal suspensions, i.e., the forced motion of a singled-out tracer particle by an external force, both in the framework of MCT and via event-driven Brownian Dynamics simulations.

Three-particle correlation functions of quasi-two-dimensional one-component and binary colloid suspensions.

Science.gov (United States)

Ho, Hau My; Lin, Binhua; Rice, Stuart A

2006-11-14

We report the results of experimental determinations of the triplet correlation functions of quasi-two-dimensional one-component and binary colloid suspensions in which the colloid-colloid interaction is short ranged. The suspensions studied range in density from modestly dilute to solid. The triplet correlation function of the one-component colloid system reveals extensive ordering deep in the liquid phase. At the same density the ordering of the larger diameter component in a binary colloid system is greatly diminished by a very small amount of the smaller diameter component. The possible utilization of information contained in the triplet correlation function in the theory of melting of a quasi-two-dimensional system is briefly discussed.

Van der Waals-like instability in suspensions of mutually repelling charged colloids

NARCIS (Netherlands)

Roij, R. van; Hansen, J.-P.

1997-01-01

We show theoretically that the purely repulsive screened-Coulomb (or Derjaguin-Landau-Verwey- Overbeek) interaction between charged colloidal particles is compatible with gas-liquid, gas-solid, and solid-solid coexistence in colloidal suspensions of low ionic strength of about 1026

Convection in a colloidal suspension in a closed horizontal cell

International Nuclear Information System (INIS)

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

2015-01-01

The experimentally detected [1] oscillatory regimes of convection in a colloidal suspension of nanoparticles with a large anomalous thermal diffusivity in a closed horizontal cell heated from below have been simulated numerically. The concentration inhomogeneity near the vertical cavity boundaries arising from the interaction of thermal-diffusion separation and convective mixing has been proven to serve as a source of oscillatory regimes (traveling waves). The dependence of the Rayleigh number at the boundary of existence of the traveling-wave regime on the aspect ratio of the closed cavity has been established. The spatial characteristics of the emerging traveling waves have been determined

A Navier-Stokes phase-field crystal model for colloidal suspensions.

Science.gov (United States)

Praetorius, Simon; Voigt, Axel

2015-04-21

We develop a fully continuous model for colloidal suspensions with hydrodynamic interactions. The Navier-Stokes Phase-Field Crystal model combines ideas of dynamic density functional theory with particulate flow approaches and is derived in detail and related to other dynamic density functional theory approaches with hydrodynamic interactions. The derived system is numerically solved using adaptive finite elements and is used to analyze colloidal crystallization in flowing environments demonstrating a strong coupling in both directions between the crystal shape and the flow field. We further validate the model against other computational approaches for particulate flow systems for various colloidal sedimentation problems.

Measurement of the effective refractive index of a turbid colloidal suspension using light refraction

International Nuclear Information System (INIS)

Reyes-Coronado, A; Garcia-Valenzuela, A; Sanchez-Perez, C; Barrera, R G

2005-01-01

We propose and analyse a simple method to measure simultaneously the real and imaginary parts of the effective refractive index of a turbid suspension of particles. The method is based on measurements of the angle of refraction and transmittance of a laser beam that traverses a hollow glass prism filled with a colloidal suspension. We provide a comprehensive assessment of the method. It can offer high sensitivity while still being simple to interpret. We present results of experiments using an optically turbid suspension of polystyrene particles and compare them with theoretical predictions. We also report experimental evidence showing that the refractive behaviour of the diffuse component of light coming from a suspension depends on the volume fraction of the colloidal particles

Aqueous suspensions of carbon nanotubes: surface oxidation, colloidal stability and uranium sorption.

Science.gov (United States)

Schierz, A; Zänker, H

2009-04-01

The objective of this study is to obtain information on the behaviour of carbon nanotubes (CNTs) as potential carriers of pollutants in the case of accidental CNT release to the environment and on the properties of CNTs as a potential adsorbent material in water purification. The effects of acid treatment of CNTs on (i) the surface properties, (ii) the colloidal stability and (iii) heavy metal sorption are investigated, the latter being exemplified by uranium(VI) sorption. There is a pronounced influence of surface treatment on the behaviour of the CNTs in aqueous suspension. Results showed that acid treatment increases the amount of acidic surface groups on the CNTs. Therefore, acid treatment has an increasing effect on the colloidal stability of the CNTs and on their adsorption capacity for U(VI). Another way to stabilise colloids of pristine CNTs in aqueous suspension is the addition of humic acid.

Long time diffusion in suspensions of interacting charged colloids

NARCIS (Netherlands)

Schepper, I.M. de; Cohen, E.G.D.; Pusey, P.N.; Lekkerkerker, H.N.W.

1989-01-01

A new expression is given for the long time diffusion coefficient DL(k) of charged interacting colloidal spheres in suspension, as a function of the wavenumber k, near k = km, where the static structure factor has a maximum. The expression is based on a physical analogy between a mode description

Kinetics of ergodic-to-nonergodic transitions in charged colloidal suspensions : aging and gelation

NARCIS (Netherlands)

Tanaka, H.; Jabbari-Farouji, S.; Meunier, J.; Bonn, D.

2005-01-01

There are two types of isotropic disordered nonergodic states in colloidal suspensions: colloidal glasses and gels. In a recent paper [H. Tanaka, J. Meunier, and D. Bonn, Phys. Rev. E 69, 031404 (2004)], we discussed the static aspect of the differences and the similarities between the two. In this

Accelerated lattice Boltzmann model for colloidal suspensions rheology and interface morphology

Science.gov (United States)

Farhat, Hassan

Colloids are ubiquitous in the food, medical, cosmetic, polymer, water purification and pharmaceutical industries. Colloids thermal, mechanical and storage properties are highly dependent on their interface morphology and their rheological behavior. Numerical methods provide a cheap and reliable virtual laboratory for the study of colloids. However efficiency is a major concern to address when using numerical methods for practical applications. This work introduces the main building-blocks for an improved lattice Boltzmann-based numerical tool designed for the study of colloidal rheology and interface morphology. The efficiency of the proposed model is enhanced by using the recently developed and validated migrating multi-block algorithms for the lattice Boltzmann method (LBM). The migrating multi-block was used to simulate single component, multi-component, multiphase and single component multiphase flows. Results were validated by experimental, numerical and analytical solutions. The contamination of the fluid-fluid interface influences the colloids morphology. This issue was addressed by the introduction of the hybrid LBM for surfactant-covered droplets. The module was used for the simulation of surfactant-covered droplet deformation under shear and uniaxial extensional flows respectively and under buoyancy. Validation with experimental and theoretical results was provided. Colloids are non-Newtonian fluids which exhibit rich rheological behavior. The suppression of coalescence module is the part of the proposed model which facilitates the study of colloids rheology. The model results for the relative viscosity were in agreement with some theoretical results. Biological suspensions such as blood are macro-colloids by nature. The study of the blood flow in the microvasculature was heuristically approached by assuming the red blood cells as surfactant covered droplets. The effects of interfacial tension on the flow velocity and the droplet exclusion from the walls

Nonequilibrium Equation of State in Suspensions of Active Colloids

Directory of Open Access Journals (Sweden)

Félix Ginot

2015-01-01

Full Text Available Active colloids constitute a novel class of materials composed of colloidal-scale particles locally converting chemical energy into motility, mimicking micro-organisms. Evolving far from equilibrium, these systems display structural organizations and dynamical properties distinct from thermalized colloidal assemblies. Harvesting the potential of this new class of systems requires the development of a conceptual framework to describe these intrinsically nonequilibrium systems. We use sedimentation experiments to probe the nonequilibrium equation of state of a bidimensional assembly of active Janus microspheres and conduct computer simulations of a model of self-propelled hard disks. Self-propulsion profoundly affects the equation of state, but these changes can be rationalized using equilibrium concepts. We show that active colloids behave, in the dilute limit, as an ideal gas with an activity-dependent effective temperature. At finite density, increasing the activity is similar to increasing adhesion between equilibrium particles. We quantify this effective adhesion and obtain a unique scaling law relating activity and effective adhesion in both experiments and simulations. Our results provide a new and efficient way to understand the emergence of novel phases of matter in active colloidal suspensions.

Phase behaviour and dynamics of suspensions of hard colloidal platelets

NARCIS (Netherlands)

Kooij, F.M. van der

2000-01-01

In this thesis we aim to provide a many-sided answer to the question: what are the consequences of plate-like colloidal shape on a suspensions' physical properties? A central role in this investigation is played by the experimental model system of platelets which, building on the Van 't Hoff

Particle-scale structure in frozen colloidal suspensions from small-angle x-ray scattering

KAUST Repository

Spannuth, Melissa

2011-02-01

During directional solidification of the solvent in a colloidal suspension, the colloidal particles segregate from the growing solid, forming high-particle-density regions with structure on a hierarchy of length scales ranging from that of the particle-scale packing to the large-scale spacing between these regions. Previous work has concentrated mostly on the medium- to large-length scale structure, as it is the most accessible and thought to be more technologically relevant. However, the packing of the colloids at the particle scale is an important component not only in theoretical descriptions of the segregation process, but also to the utility of freeze-cast materials for new applications. Here we present the results of experiments in which we investigated this structure across a wide range of length scales using a combination of small-angle x-ray scattering and direct optical imaging. As expected, during freezing the particles were concentrated into regions between ice dendrites forming a microscopic pattern of high- and low-particle-density regions. X-ray scattering indicates that the particles in the high-density regions were so closely packed as to be touching. However, the arrangement of the particles does not conform to that predicted by standard interparticle pair potentials, suggesting that the particle packing induced by freezing differs from that formed during equilibrium densification processes. © 2011 American Physical Society.

Particle-scale structure in frozen colloidal suspensions from small-angle x-ray scattering

KAUST Repository

Spannuth, Melissa; Mochrie, S. G. J.; Peppin, S. S. L.; Wettlaufer, J. S.

2011-01-01

During directional solidification of the solvent in a colloidal suspension, the colloidal particles segregate from the growing solid, forming high-particle-density regions with structure on a hierarchy of length scales ranging from that of the particle-scale packing to the large-scale spacing between these regions. Previous work has concentrated mostly on the medium- to large-length scale structure, as it is the most accessible and thought to be more technologically relevant. However, the packing of the colloids at the particle scale is an important component not only in theoretical descriptions of the segregation process, but also to the utility of freeze-cast materials for new applications. Here we present the results of experiments in which we investigated this structure across a wide range of length scales using a combination of small-angle x-ray scattering and direct optical imaging. As expected, during freezing the particles were concentrated into regions between ice dendrites forming a microscopic pattern of high- and low-particle-density regions. X-ray scattering indicates that the particles in the high-density regions were so closely packed as to be touching. However, the arrangement of the particles does not conform to that predicted by standard interparticle pair potentials, suggesting that the particle packing induced by freezing differs from that formed during equilibrium densification processes. © 2011 American Physical Society.

Convective flows of colloidal suspension in an inclined closed cell

Energy Technology Data Exchange (ETDEWEB)

Smorodin, Boris; Ishutov, Sergey [Department of Physics of Phase Transitions, Perm State University, Perm (Russian Federation); Cherepanov, Ivan, E-mail: bsmorodin@yandex.ru [Department of Radio Electronics and Information Security, Perm State University, Perm (Russian Federation)

2016-12-15

The nonlinear spatiotemporal evolution of convective flows is numerically investigated in the case of colloidal suspension filling an inclined closed cell heated from below. The bifurcation diagram (the dependency of the Nusselt number on the Rayleigh number) is obtained. The characteristics of the wave and steady patterns are investigated depending on heat intensity. The travelling wave changing travel direction and the non-regular oscillatory flow are found to be stable solutions within a certain interval of the Rayleigh number. Temporal Fourier decomposition is used together with other diagnostic tools to analyse the complex bifurcation and spatiotemporal properties caused by the interplay of the gravity-induced gradient of concentration and convective mixing of the fluid. It is shown that a more complex flow structure exists at a lower heating intensity (Rayleigh number). (paper)

Optical limiting in gelatin stabilized Cu-PVP nanocomposite colloidal suspension

Science.gov (United States)

Tamgadge, Y. S.; Gedam, P. P.; Thakare, N. B.; Talwatkar, S. S.; Sunatkari, A. L.; Muley, G. G.

2018-05-01

This article illustrates investigations on optical limiting properties of Cu-PVP nanocomposite colloidal suspension. Gelatin stabilized Cu nanoparticles have been synthesized using chemical reduction method and thin films in PVP matrix have been obtained using spin coating technique. Thin films have been characterized by X-ray diffraction (XRD), Ultraviolet-visible (UV-vis) spectroscopy, etc. for structural and linear optical studies. Optical limiting properties of Colloidal Cu-PVP nanocomposites have been investigated at 808 nm diode CW laser. Minimum optical limiting threshold was found for GCu3-PVP nanocomposites sample. The strong optical limiting is thermal in origin as CW laser is used and effects are attributed to thermal lensing effect.

Active colloids

International Nuclear Information System (INIS)

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. (physics of our days)

Colloidal Photoluminescent Amorphous Porous Silicon, Methods Of Making Colloidal Photoluminescent Amorphous Porous Silicon, And Methods Of Using Colloidal Photoluminescent Amorphous Porous Silicon

KAUST Repository

Chaieb, Sahraoui

2015-04-09

Embodiments of the present disclosure provide for a colloidal photoluminescent amorphous porous silicon particle suspension, methods of making a colloidal photoluminescent amorphous porous silicon particle suspension, methods of using a colloidal photoluminescent amorphous porous silicon particle suspension, and the like.

Colloidal Photoluminescent Amorphous Porous Silicon, Methods Of Making Colloidal Photoluminescent Amorphous Porous Silicon, And Methods Of Using Colloidal Photoluminescent Amorphous Porous Silicon

KAUST Repository

Chaieb, Saharoui; Mughal, Asad Jahangir

2015-01-01

Embodiments of the present disclosure provide for a colloidal photoluminescent amorphous porous silicon particle suspension, methods of making a colloidal photoluminescent amorphous porous silicon particle suspension, methods of using a colloidal photoluminescent amorphous porous silicon particle suspension, and the like.

Equivalence of Brownian dynamics and dynamic Monte Carlo simulations in multicomponent colloidal suspensions.

Science.gov (United States)

Cuetos, Alejandro; Patti, Alessandro

2015-08-01

We propose a simple but powerful theoretical framework to quantitatively compare Brownian dynamics (BD) and dynamic Monte Carlo (DMC) simulations of multicomponent colloidal suspensions. By extending our previous study focusing on monodisperse systems of rodlike colloids, here we generalize the formalism described there to multicomponent colloidal mixtures and validate it by investigating the dynamics in isotropic and liquid crystalline phases containing spherical and rodlike particles. In order to investigate the dynamics of multicomponent colloidal systems by DMC simulations, it is key to determine the elementary time step of each species and establish a unique timescale. This is crucial to consistently study the dynamics of colloidal particles with different geometry. By analyzing the mean-square displacement, the orientation autocorrelation functions, and the self part of the van Hove correlation functions, we show that DMC simulation is a very convenient and reliable technique to describe the stochastic dynamics of any multicomponent colloidal system. Our theoretical formalism can be easily extended to any colloidal system containing size and/or shape polydisperse particles.

Structure and stability of charged colloid-nanoparticle mixtures

Science.gov (United States)

Weight, Braden M.; Denton, Alan R.

2018-03-01

Physical properties of colloidal materials can be modified by addition of nanoparticles. Within a model of like-charged mixtures of particles governed by effective electrostatic interactions, we explore the influence of charged nanoparticles on the structure and thermodynamic phase stability of charge-stabilized colloidal suspensions. Focusing on salt-free mixtures of particles of high size and charge asymmetry, interacting via repulsive Yukawa effective pair potentials, we perform molecular dynamics simulations and compute radial distribution functions and static structure factors. Analysis of these structural properties indicates that increasing the charge and concentration of nanoparticles progressively weakens correlations between charged colloids. We show that addition of charged nanoparticles to a suspension of like-charged colloids can induce a colloidal crystal to melt and can facilitate aggregation of a fluid suspension due to attractive van der Waals interactions. We attribute the destabilizing influence of charged nanoparticles to enhanced screening of electrostatic interactions, which weakens repulsion between charged colloids. This interpretation is consistent with recent predictions of an effective interaction theory of charged colloid-nanoparticle mixtures.

Pore water colloid properties in argillaceous sedimentary rocks

Energy Technology Data Exchange (ETDEWEB)

Degueldre, Claude, E-mail: c.degueldre@lancaster.ac.uk [Engineering Department, University of Lancaster, LA1 4YW Lancaster (United Kingdom); ChiAM & Institute of Environment, University of Geneva, 1211 Genève 4, Swizerland (Switzerland); Earlier, NES, Paul Scherrer Institute, 5232 Villigen (Switzerland); Cloet, Veerle [NAGRA, Hardstrasse 73, 5430 Wettingen (Switzerland)

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

Imaging the Microscopic Structure of Shear Thinning and Thickening Colloidal Suspensions

KAUST Repository

Cheng, X.

2011-09-01

The viscosity of colloidal suspensions varies with shear rate, an important effect encountered in many natural and industrial processes. Although this non-Newtonian behavior is believed to arise from the arrangement of suspended particles and their mutual interactions, microscopic particle dynamics are difficult to measure. By combining fast confocal microscopy with simultaneous force measurements, we systematically investigate a suspension\\'s structure as it transitions through regimes of different flow signatures. Our measurements of the microscopic single-particle dynamics show that shear thinning results from the decreased relative contribution of entropic forces and that shear thickening arises from particle clustering induced by hydrodynamic lubrication forces. This combination of techniques illustrates an approach that complements current methods for determining the microscopic origins of non-Newtonian flow behavior in complex fluids.

Boundary Effects and Shear Thickening of Colloidal Suspensions: A study based on measurement of Suspension Microstructure

Science.gov (United States)

Perera, M. Tharanga D.

Microstructure is key to understanding rheological behaviors of flowing particulate suspensions. During the past decade, Stokesian Dynamics simulations have been the dominant method of determining suspension microstructure. Structure results obtained numerically reveal that an anisotropic structure is formed under high Peclet (Pe) number conditions. Researchers have used various experimental techniques such as small angle neutron scattering (SANS) and light scattering methods to validate microstructure. This work outlines an experimental technique based on confocal microscopy to study microstructure of a colloidal suspension in an index-matched fluid flowing in a microchannel. High resolution scans determining individual particle locations in suspensions 30-50 vol % yield quantitative results of the local microstructure in the form of the pair distribution function, g(r). From these experimentally determined g(r), the effect of shear rate, quantified by the Peclet number as a ratio of shear and Brownian stress, on the suspension viscosity and normal stress follow that seen in macroscopic rheological measurements and simulations. It is generally believed that shear thickening behavior of colloidal suspensions is driven by the formation of hydroclusters. From measurements of particle locations, hydroclusters are identified. The number of hydroclusters grows exponentially with increasing Pe, and the onset of shear thickening is driven by the increase in formation of clusters having 5-8 particles. At higher Pe, we notice the emergence of 12 or more particle clusters. The internal structure of these hydroclusters has been investigated, and there is some evidence that particles internal to hydroclusters preferentially align along the 45° and 135° axis. Beyond observations of bulk suspension behavior, the influence of boundaries on suspension microstructure is also investigated. Experiments were performed for suspensions flowing over smooth walls, made of glass

The physics of the colloidal glass transition.

Science.gov (United States)

Hunter, Gary L; Weeks, Eric R

2012-06-01

As one increases the concentration of a colloidal suspension, the system exhibits a dramatic increase in viscosity. Beyond a certain concentration, the system is said to be a colloidal glass; structurally, the system resembles a liquid, yet motions within the suspension are slow enough that it can be considered essentially frozen. For several decades, colloids have served as a valuable model system for understanding the glass transition in molecular systems. The spatial and temporal scales involved allow these systems to be studied by a wide variety of experimental techniques. The focus of this review is the current state of understanding of the colloidal glass transition, with an emphasis on experimental observations. A brief introduction is given to important experimental techniques used to study the glass transition in colloids. We describe features of colloidal systems near and in glassy states, including increases in viscosity and relaxation times, dynamical heterogeneity and ageing, among others. We also compare and contrast the glass transition in colloids to that in molecular liquids. Other glassy systems are briefly discussed, as well as recently developed synthesis techniques that will keep these systems rich with interesting physics for years to come.

The physics of the colloidal glass transition

International Nuclear Information System (INIS)

Hunter, Gary L; Weeks, Eric R

2012-01-01

As one increases the concentration of a colloidal suspension, the system exhibits a dramatic increase in viscosity. Beyond a certain concentration, the system is said to be a colloidal glass; structurally, the system resembles a liquid, yet motions within the suspension are slow enough that it can be considered essentially frozen. For several decades, colloids have served as a valuable model system for understanding the glass transition in molecular systems. The spatial and temporal scales involved allow these systems to be studied by a wide variety of experimental techniques. The focus of this review is the current state of understanding of the colloidal glass transition, with an emphasis on experimental observations. A brief introduction is given to important experimental techniques used to study the glass transition in colloids. We describe features of colloidal systems near and in glassy states, including increases in viscosity and relaxation times, dynamical heterogeneity and ageing, among others. We also compare and contrast the glass transition in colloids to that in molecular liquids. Other glassy systems are briefly discussed, as well as recently developed synthesis techniques that will keep these systems rich with interesting physics for years to come. (review article)

Pore water colloid properties in argillaceous sedimentary rocks.

Science.gov (United States)

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

Nonlinear oscillatory rheology and structure of wormlike micellar solutions and colloidal suspensions

Science.gov (United States)

Gurnon, Amanda Kate

The complex, nonlinear flow behavior of soft materials transcends industrial applications, smart material design and non-equilibrium thermodynamics. A long-standing, fundamental challenge in soft-matter science is establishing a quantitative connection between the deformation field, local microstructure and macroscopic dynamic flow properties i.e., the rheology. Soft materials are widely used in consumer products and industrial processes including energy recovery, surfactants for personal healthcare (e.g. soap and shampoo), coatings, plastics, drug delivery, medical devices and therapeutics. Oftentimes, these materials are processed by, used during, or exposed to non-equilibrium conditions for which the transient response of the complex fluid is critical. As such, designing new dynamic experiments is imperative to testing these materials and further developing micromechanical models to predict their transient response. Two of the most common classes of these soft materials stand as the focus of the present research; they are: solutions of polymer-like micelles (PLM or also known as wormlike micelles, WLM) and concentrated colloidal suspensions. In addition to their varied applications these two different classes of soft materials are also governed by different physics. In contrast, to the shear thinning behavior of the WLMs at high shear rates, the near hard-sphere colloidal suspensions are known to display increases, sometimes quite substantial, in viscosity (known as shear thickening). The stress response of these complex fluids derive from the shear-induced microstructure, thus measurements of the microstructure under flow are critical for understanding the mechanisms underlying the complex, nonlinear rheology of these complex fluids. A popular micromechanical model is reframed from its original derivation for predicting steady shear rheology of polymers and WLMs to be applicable to weakly nonlinear oscillatory shear flow. The validity, utility and limits of

Study of shear thickening behavior in colloidal suspensions

Directory of Open Access Journals (Sweden)

N Maleki Jirsaraee

2015-01-01

Full Text Available We studied the shear thickening behavior of the nano silica suspension (silica nanoparticles 12 nm in size suspended in ethylene glycol under steady shear. The critical shear rate for transition into shear thickening phase was determined at different concentrations and temperatures. The effect of temperature and concentration was studied on the shear thickening behavior. In silica suspension, it was observed that all the samples had a transition into shear thickening phase and also by increasing the temperature, critical shear rate increased and viscosity decreased. Our observations showed that movement in silica suspension was Brownian and temperature could cause a delay in transition into shear thickening phase. Yet, we observed that increasing the concentration would decrease critical shear rate and increase viscosity. Increasing temperature increased Brownian forces and increasing concentration increased hydrodynamic forces, confirming the contrast between these two forces for transition into shear thickening phase for the suspensions containing nano particles

Fast technetium Eigen-colloid determination: preparative CPC combined with suspension liquid scintillation

International Nuclear Information System (INIS)

Breynaert, E.; Maes, A.

2005-01-01

Full text of publication follows: Both medical and environmental studies concerned with the solubility and the complexation chemistry of technetium have encountered colloidal Tc(IV)-forms. Although the existence of the Tc colloids has been proven by various techniques [1-6], their determination still remains an issue. Recently a Column Precipitation Chromatography (CPC) technique was developed which enabled the quantitative determination of technetium Eigen-colloids. Based on this technique, a solid phase extraction (SPE)-like methodology was developed that can be used in combination with suspension liquid scintillation to provide a fast analysis of the Eigen-colloid content of a sample. The CPC technique is a thorough analysis methodology for the quantitative determination of the Eigen-colloid content of a sample containing reduced technetium species. This technique requires a relative long elution scheme and fractionation of the eluate. The fractionation also implies a relatively long counting time to determine the Eigen-colloid activity of a sample. Currently an SPE-like analysis methodology was developed which combines a good estimate of the Eigen-colloid content with fast analysis times. To construct a methodology providing both features a specialized extraction apparatus was constructed and a quantitative suspension liquid scintillation technique was developed. This combination enables the Eigen-colloid determination within a short experimental time (15 min) and a limited counting time (60 min). The authors acknowledge a grant from KULeuven University and financial support from the KULeuven Geconcerteerde Onderzoeksacties (GOA2000/007). We also kindly acknowledge NIRAS/ONDRAF for financial support from Contract CCHO 20004004862 [1] Grossmann, B. and R. Muenze, Relationship between complex formation by 99 Tc(IV) and the chemical structure of aliphatic carboxylic acid ligands. The International Journal of Applied Radiation and Isotopes, 1982. 33(3): p. 189

Laser diffraction analysis of colloidal crystals

Energy Technology Data Exchange (ETDEWEB)

Sogami, Ikuo S.; Shinohara, Tadatomi; Yoshiyama, Tsuyoshi [Kyoto Sangyo Univ., Department of Physics, Kyoto (Japan)

2001-10-01

Laser diffraction analysis is made on crystallization in salt-free aqueous suspensions of highly-charged colloidal particles for semi-dilute specimens of concentration 0.1-10.0 vol%. Kossel diffraction patterns which represent faithfully accurate information on lattice symmetries in the suspensions enable us to investigate the time evolution of colloidal crystals. The results show that the crystallization proceeds by way of the following intermediate phase transitions: two-dimensional hcp structure {yields} random layer structure {yields} layer structure with one sliding degree of freedom {yields} stacking disorder structure {yields} stacking structure with multivariant periodicity {yields} fcc twin structure with twin plane (111) {yields} normal fcc structure {yields} bcc twin structure with twin plane (11-bar2) or (1-bar12) {yields} normal bcc structure. For concentrated suspensions (>2 vol %), the phase transition ceases to proceed at the normal fcc structure. (author)

Laser diffraction analysis of colloidal crystals

International Nuclear Information System (INIS)

Sogami, Ikuo S.; Shinohara, Tadatomi; Yoshiyama, Tsuyoshi

2001-01-01

Laser diffraction analysis is made on crystallization in salt-free aqueous suspensions of highly-charged colloidal particles for semi-dilute specimens of concentration 0.1-10.0 vol%. Kossel diffraction patterns which represent faithfully accurate information on lattice symmetries in the suspensions enable us to investigate the time evolution of colloidal crystals. The results show that the crystallization proceeds by way of the following intermediate phase transitions: two-dimensional hcp structure → random layer structure → layer structure with one sliding degree of freedom → stacking disorder structure → stacking structure with multivariant periodicity → fcc twin structure with twin plane (111) → normal fcc structure → bcc twin structure with twin plane (11-bar2) or (1-bar12) → normal bcc structure. For concentrated suspensions (>2 vol %), the phase transition ceases to proceed at the normal fcc structure. (author)

Structure and dynamics of soft repulsive colloidal suspensions in the vicinity of the glass transition.

Science.gov (United States)

Crassous, Jérôme J; Casal-Dujat, Lucia; Medebach, Martin; Obiols-Rabasa, Marc; Vincent, Romaric; Reinhold, Frank; Boyko, Volodymyr; Willerich, Immanuel; Menzel, Andreas; Moitzi, Christian; Reck, Bernd; Schurtenberger, Peter

2013-08-20

We use a combination of different scattering techniques and rheology to highlight the link between structure and dynamics of dense aqueous suspensions of soft repulsive colloids in the vicinity of a glass transition. Three different latex formulations with an increasing amount of the hydrophilic component resulting in either purely electrostatically or electrosterically stabilized suspensions are investigated. From the analysis of the static structure factor measured by small-angle X-ray scattering, we derive an effective volume fraction that includes contributions from interparticle interactions. We further investigate the dynamics of the suspensions using 3D cross-correlation dynamic light scattering (3DDLS) and rheology. We analyze the data using an effective hard sphere model and in particular compare the linear viscoelasticity and flow behavior to the predictions of mode coupling theory, which accounts for a purely kinetic glass transition determined by the equilibrium structure factor. We demonstrate that seemingly very different colloidal systems exhibit the same generic behavior when the effects from interparticle interactions are incorporated using an effective volume fraction description.

Structure of colloidal sphere-plate mixtures

International Nuclear Information System (INIS)

Doshi, N; Cinacchi, G; Van Duijneveldt, J S; Cosgrove, T; Prescott, S W; Grillo, I; Phipps, J; Gittins, D I

2011-01-01

In addition to containing spherical pigment particles, coatings usually contain plate-like clay particles. It is thought that these improve the opacity of the paint film by providing an efficient spacing of the pigment particles. This observation is counterintuitive, as suspensions of particles of different shapes and sizes tend to phase separate on increase of concentration. In order to clarify this matter a model colloidal system is studied here, with a sphere-plate diameter ratio similar to that found in paints. For dilute suspensions, small angle neutron scattering revealed that the addition of plates leads to enhanced density fluctuations of the spheres, in agreement with new theoretical predictions. On increasing the total colloid concentration the plates and spheres phase separate due to the disparity in their shape. This is in agreement with previous theoretical and experimental work on colloidal sphere-plate mixtures, where one particle acts as a depleting agent. The fact that no large scale phase separation is observed in coatings is ascribed to dynamic arrest in intimately mixed, or possibly micro-phase separated structures, at elevated concentration.

Structure of colloidal sphere-plate mixtures

Energy Technology Data Exchange (ETDEWEB)

Doshi, N; Cinacchi, G; Van Duijneveldt, J S; Cosgrove, T; Prescott, S W [School of Chemistry, University of Bristol, Bristol BS8 1TS (United Kingdom); Grillo, I [Institut Laue-Langevin, 6 rue Jules Horowitz BP 156, 38042 Grenoble Cedex 9 (France); Phipps, J [Imerys Minerals Ltd, Par Moor Centre, Par Moor Road, Par, Cornwall PL24 2SQ (United Kingdom); Gittins, D I, E-mail: Giorgio.Cinacchi@bristol.ac.uk, E-mail: J.S.van-Duijneveldt@bristol.ac.uk [Imerys Performance and Filtration Minerals Ltd, 130 Castilian Drive, Goleta, CA 93117 (United States)

2011-05-18

In addition to containing spherical pigment particles, coatings usually contain plate-like clay particles. It is thought that these improve the opacity of the paint film by providing an efficient spacing of the pigment particles. This observation is counterintuitive, as suspensions of particles of different shapes and sizes tend to phase separate on increase of concentration. In order to clarify this matter a model colloidal system is studied here, with a sphere-plate diameter ratio similar to that found in paints. For dilute suspensions, small angle neutron scattering revealed that the addition of plates leads to enhanced density fluctuations of the spheres, in agreement with new theoretical predictions. On increasing the total colloid concentration the plates and spheres phase separate due to the disparity in their shape. This is in agreement with previous theoretical and experimental work on colloidal sphere-plate mixtures, where one particle acts as a depleting agent. The fact that no large scale phase separation is observed in coatings is ascribed to dynamic arrest in intimately mixed, or possibly micro-phase separated structures, at elevated concentration.

Aqueous Colloid + Polymer Depletion System for Confocal Microscopy and Rheology

Science.gov (United States)

Park, Nayoung; Umanzor, Esmeralda J.; Conrad, Jacinta C.

2018-05-01

We developed a model depletion system with colloidal particles that were refractive index- and density-matched to 80 (w/w)% glycerol in water, and characterized the effect of interparticle interactions on the structure and dynamics of non-equilibrium phases. 2,2,2-trifluoroethyl methacrylate-co-tert-butyl methacrylate copolymer particles were synthesized following Kodger et al. (Sci. Rep. 5, 14635 (2015)). Particles were dispersed in glycerol/water solutions to generate colloidal suspensions with good control over electrostatic interactions and a moderately high background viscosity of 55 mPa-s. To probe the effects of charge screening and depletion attractions on the suspension phase behavior, we added NaCl and polyacrylamide (M_w = 186 kDa) at various concentrations to particle suspensions formulated at volume fractions of phi = 0.05 and 0.3 and imaged the suspensions using confocal microscopy. The particles were nearly hard spheres at a NaCl concentration of 20 mM, but aggregated when the concentration of NaCl was further increased. Changes in the particle structure and dynamics with increasing concentration of the depletant polyacrylamide followed the trends expected from earlier experiments on depletion-driven gelation. Additionally, we measured the viscosity and corrected first normal stress difference of suspensions formulated at phi = 0.4 with and without added polymer. The solvent viscosity was suitable for rheology measurements without the onset of instabilities such as secondary flows or edge fracture. These results validate this system as an alternative to one common model system, suspensions of poly(methyl methacrylate) particles and polystyrene depletants in organic solvents, for investigating phase behavior and flow properties in attractive colloidal suspensions.

Analytical scale purification of zirconia colloidal suspension using field programmed sedimentation field flow fractionation.

Science.gov (United States)

Van-Quynh, Alexandra; Blanchart, Philippe; Battu, Serge; Clédat, Dominique; Cardot, Philippe

2006-03-03

Sedimentation field flow fractionation was used to obtain purified fractions from a polydispersed zirconia colloidal suspension in the potential purpose of optical material hybrid coating. The zirconia particle size ranged from 50/70 nm to 1000 nm. It exhibited a log-Gaussian particle size distribution (in mass or volume) and a 115% polydispersity index (P.I.). Time dependent eluted fractions of the original zirconia colloidal suspension were collected. The particle size distribution of each fraction was determined with scanning electron microscopy and Coulter sub-micron particle sizer (CSPS). These orthogonal techniques generated similar data. From fraction average elution times and granulometry measurements, it was shown that zirconia colloids are eluted according to the Brownian elution mode. The four collected fractions have a Gaussian like distribution and respective average size and polydispersity index of 153 nm (P.I. = 34.7%); 188 nm (P.I. = 27.9%); 228 nm (P.I. = 22.6%), and 276 nm (P.I. = 22.3%). These data demonstrate the strong size selectivity of SdFFF operated with programmed field of exponential profile for sorting particles in the sub-micron range. Using this technique, the analytical production of zirconia of given average size and reduced polydispersity is possible.

Orientational Order of Carbon Nanotube Guests in a Nematic Host Suspension of Colloidal Viral Rods

NARCIS (Netherlands)

Puech, N.; Dennison, M.; Blanc, C.; van der Schoot, P.; van Roij, R.; Poulin, P.; Grelet, E.

2012-01-01

In order to investigate the coupling between the degrees of alignment of elongated particles in binary nematic dispersions, surfactant stabilized single-wall carbon nanotubes (CNTs) have been added to nematic suspensions of colloidal rodlike viruses in aqueous solution. We have independently

Orientational order of carbon nanotube guests in a nematic host suspension of colloidal viral rods

NARCIS (Netherlands)

Puech, N.; Dennison, M.; Blanc, C.; Schoot, van der P.P.A.M.; Dijkstra, Marjolein; Roij, van R.; Poulin, P.; Grelet, E.

2012-01-01

In order to investigate the coupling between the degrees of alignment of elongated particles in binary nematic dispersions, surfactant stabilized single-wall carbon nanotubes (CNTs) have been added to nematic suspensions of colloidal rodlike viruses in aqueous solution. We have independently

Formation of a barrier to groundwater contaminants by the injection of zero-valent iron colloids: Suspension properties

International Nuclear Information System (INIS)

Kaplan, D.I.; Cantrell, K.J.; Wietsma, T.W.

1994-01-01

Zero-valent iron (Fe 0 ) (metallic iron) is a strong chemical reductant that is capable of degrading several halogenated-hydrocarbon compounds (e.g., trichloroethene and tetrachloroethene) and chemically reducing several highly mobile oxidized oxyanions and oxycations to their immobile forms. A series of studies was undertaken to develop methods of injecting micrometer-sized Fe 0 colloids into the subsurface environment to form a chemical barrier to these highly mobile contaminants. Forming a barrier by means of this technique may have the distinct advantage over traditional trench-and-fill technologies: it may be safer, more cost-effective, and may be used at greater depths. Several commercially available Fe 0 colloids were evaluated. One type was selected for further study based on its small size (1 to 2 microm) and the presence of an organic coating. This organic coating was weathered away within 7 days by Hanford ground water (CaCO 3 system, pH 8.1) and exposed the chemically active Fe 0 -colloid surface. Through the use of surfactants in a low ionic strength solution, the length of time that these extremely dense (7.8 g cm -3 ) colloids remained in suspension increased as much as 250%. The efficiency of quartz-sand columns to remove surfactant-coated Fe 0 colloids appeared to be at least partially controlled by injection rate; the filter coefficient values at injection rates of 6, 124, and 248 ml min -1 were 0.30, 0.05, and 0.02 cm -1 , respectively. Studies are underway to develop further understanding of this relationship and to determine the interactive effect of influent colloid concentration and injection flow rate on colloid placement in aquifer sediments for barrier formation

Pair mobility functions for rigid spheres in concentrated colloidal dispersions: Force, torque, translation, and rotation.

Science.gov (United States)

Zia, Roseanna N; Swan, James W; Su, Yu

2015-12-14

The formulation of detailed models for the dynamics of condensed soft matter including colloidal suspensions and other complex fluids requires accurate description of the physical forces between microstructural constituents. In dilute suspensions, pair-level interactions are sufficient to capture hydrodynamic, interparticle, and thermodynamic forces. In dense suspensions, many-body interactions must be considered. Prior analytical approaches to capturing such interactions such as mean-field approaches replace detailed interactions with averaged approximations. However, long-range coupling and effects of concentration on local structure, which may play an important role in, e.g., phase transitions, are smeared out in such approaches. An alternative to such approximations is the detailed modeling of hydrodynamic interactions utilizing precise couplings between moments of the hydrodynamic traction on a suspended particle and the motion of that or other suspended particles. For two isolated spheres, a set of these functions was calculated by Jeffrey and Onishi [J. Fluid Mech. 139, 261-290 (1984)] and Jeffrey [J. Phys. Fluids 4, 16-29 (1992)]. Along with pioneering work by Batchelor, these are the touchstone for low-Reynolds-number hydrodynamic interactions and have been applied directly in the solution of many important problems related to the dynamics of dilute colloidal dispersions [G. K. Batchelor and J. T. Green, J. Fluid Mech. 56, 375-400 (1972) and G. K. Batchelor, J. Fluid Mech. 74, 1-29 (1976)]. Toward extension of these functions to concentrated systems, here we present a new stochastic sampling technique to rapidly calculate an analogous set of mobility functions describing the hydrodynamic interactions between two hard spheres immersed in a suspension of arbitrary concentration, utilizing accelerated Stokesian dynamics simulations. These mobility functions provide precise, radially dependent couplings of hydrodynamic force and torque to particle translation

Pair mobility functions for rigid spheres in concentrated colloidal dispersions: Force, torque, translation, and rotation

International Nuclear Information System (INIS)

Zia, Roseanna N.; Su, Yu; Swan, James W.

2015-01-01

The formulation of detailed models for the dynamics of condensed soft matter including colloidal suspensions and other complex fluids requires accurate description of the physical forces between microstructural constituents. In dilute suspensions, pair-level interactions are sufficient to capture hydrodynamic, interparticle, and thermodynamic forces. In dense suspensions, many-body interactions must be considered. Prior analytical approaches to capturing such interactions such as mean-field approaches replace detailed interactions with averaged approximations. However, long-range coupling and effects of concentration on local structure, which may play an important role in, e.g., phase transitions, are smeared out in such approaches. An alternative to such approximations is the detailed modeling of hydrodynamic interactions utilizing precise couplings between moments of the hydrodynamic traction on a suspended particle and the motion of that or other suspended particles. For two isolated spheres, a set of these functions was calculated by Jeffrey and Onishi [J. Fluid Mech. 139, 261–290 (1984)] and Jeffrey [J. Phys. Fluids 4, 16–29 (1992)]. Along with pioneering work by Batchelor, these are the touchstone for low-Reynolds-number hydrodynamic interactions and have been applied directly in the solution of many important problems related to the dynamics of dilute colloidal dispersions [G. K. Batchelor and J. T. Green, J. Fluid Mech. 56, 375–400 (1972) and G. K. Batchelor, J. Fluid Mech. 74, 1–29 (1976)]. Toward extension of these functions to concentrated systems, here we present a new stochastic sampling technique to rapidly calculate an analogous set of mobility functions describing the hydrodynamic interactions between two hard spheres immersed in a suspension of arbitrary concentration, utilizing accelerated Stokesian dynamics simulations. These mobility functions provide precise, radially dependent couplings of hydrodynamic force and torque to particle

Cements and concentrated model suspensions. Flow, jamming and flocculation; Ciments et suspensions concentrees modeles. Ecoulement, encombrement et floculation

Energy Technology Data Exchange (ETDEWEB)

Lootens, D

2004-10-15

Here we report about the rheological behavior of very concentrated dispersions -or pastes- of granular or colloidal particles of cement or of monodisperse spherical silica particles. The model system of silica particles is used in order to control the physical chemistry properties of the suspension. Our research project is centered on two points which are focusing on the slurries properties: (i) the first one is the study of the structuring process by the coagulation at rest and its relation with setting. We use special tools (ultrasonic, confocal) to follow and understand the evolution from coagulation to the setting of cement (ii) the second is the study of the dynamic structuring phenomena, under shear, typical of the concentrated suspensions and named jamming. The flow can enter into a shear-thickening and, possibly jamming regime. The onset of this regime is shown to involve giant fluctuations of stress, assigned to the formation and breakup of direct frictional contact chains. The surface state of the particles is a determining factor in this transition. The studies of the normal stress and microscopic observation give good reasons to believe that solid friction is involved in the jamming transition. (author)

Colloidal suspensions in external rotating electric field: experimental studies and prospective applications in physics, material science, and biomedicine

Science.gov (United States)

Yakovlev, Egor V.; Troshina, Anna V.; Korsakova, Sofia A.; Andronik, Mikhail; Rodionov, Ilya A.; Aliev, Ismail N.; Zaytsev, Kirill I.; Cherkasova, Olga P.; Tuchin, Valery V.; Yurchenko, Stanislav O.

2018-04-01

Colloidal suspensions and tunable self-assembly of colloidal particles attract a great interest in recent years. In this paper, we propose a new setup and technology for studies of self-assembly of colloidal particles, interection of which between themselves is tuned by external rotating electric fields. We reveal wide prospectives of electric field employment for tunable self-assembly, from suspensions of inorganic particles to ensembles of biological cells. These results make enable particle-resolved studies of various collective phenomena and fundamental processes in many-particle systems in equilibrium state and far from it, while the dynamics can be resolved at the level of individual particles using video microscopy. For the first time, we demonstrate that, apart from ability to prepare photonic crystalline films of inorganic silica particles, the tunable self-assembly provides a novel technological way for manipulation with ensembles of biological cells by control of interactions between them.

Orientational order of carbon nanotube guests in a nematic host suspension of colloidal viral rods

NARCIS (Netherlands)

Puech, N.; Dennison, M; Blanc, C; van der Schoot, P. P. A. M.; Dijkstra, M.; Van Roij, R.; Poulin, P.; Grelet, E

2012-01-01

In order to investigate the coupling between the degrees of alignment of elongated particles in binary nematic dispersions, surfactant stabilized single-wall carbon nanotubes (CNTs) have been added to nematic suspensions of colloidal rodlike viruses in aqueous solution.We have independently measured

Colloidal suspensions hydrodynamic retention mechanisms in model porous media

International Nuclear Information System (INIS)

Salehi, N.

1996-01-01

This study deals with the retention mechanisms of colloidal particles in porous media flows, and the subsequent reduction in permeability in the case of stable and non adsorbing colloids. It combines experimental results and modelling. This study has been realised with stable dispersion of monodispersed carboxylate polystyrene latexes negatively charged injected through negatively charged polycarbonate membranes having mono-sized cylindrical pores. The mean particle diameter is smaller than the mean pore diameter. Both batch and flow experiments in Nuclepore membranes have been done. The results of batch experiments have proved no adsorption of the colloidal latex particles on the surface of the Nuclepore membranes without flow at low salinity. In flow experiments at low particle concentration, only deposition on the upstream side of the membrane have been induced by hydrodynamic forces even for non adsorbing particles without creating any permeability reduction. The retention levels are zero at low and high Peclet numbers with a maximum at intermediate values. Partial plugging was observed at higher colloid concentration even at low salinity without any upstream surface deposition. The modelling of plugging processes is achieved by considering the particle concentration, fluid rate and ratio between the mean pore diameter and the mean particle diameter. This study can be particularly useful in the fields of water treatment and of restoration of lands following radioactive contamination. (author). 96 refs., 99 figs., 29 tabs

Viscothermal Coupling Effects on Sound Attenuation in Concentrated Colloidal Dispersions.

Science.gov (United States)

Han, Wei

1995-11-01

This thesis describes a Unified Coupled Phase Continuum (UCPC) model to analyze sound propagation through aerosols, emulsions and suspensions in terms of frequency dependent attenuation coefficient and sound speed. Expressions for the viscous and thermal coupling coefficients explicitly account for the effects of particle size, shape factor, orientation as well as concentration and the sound frequency. The UCPC model also takes into account the intrinsic acoustic absorption within the fluid medium due to its viscosity and heat conductivity. The effective complex wave number as a function of frequency is derived. A frequency- and concentration-dependent complex Nusselt number for the interfacial thermal coupling coefficient is derived using an approximate similarity between the 'viscous skin drag' and 'heat conduction flux' associated with the discontinuous suspended phase, on the basis of a cell model. The theoretical predictions of attenuation spectra provide satisfactory agreement with reported experimental data on two concentrated suspensions (polystyrene latex and kaolin pigment), two concentrated emulsions (toluene -in-water, n-hexadecane-in-water), and two aerosols (oleic acid droplets-in-nitrogen, alumina-in-air), covering a wide range of relative magnitudes (from 10^ {-3} to 10^{3}) of thermal versus viscous contributions, for dispersed phase volume fractions as high as 50%. The relative differences between the additive result of separate viscous and thermal loss estimates and combined viscothermal absorption results are also presented. Effects of particle shape on viscous attenuation of sound in concentrated suspensions of non-spherical clay particles are studied. Attenuation spectra for 18 frequencies from 3 to 100 MHz are measured and analyzed for eleven kaolin clay slurries with solid concentrations ranging from 0.6% to 35% (w/w). A modified viscous drag coefficient that considers frequency, concentration, particle size, shape and orientation of

Pt based PEMFC catalysts prepared from colloidal particle suspensions--a toolbox for model studies.

Science.gov (United States)

Speder, Jozsef; Altmann, Lena; Roefzaad, Melanie; Bäumer, Marcus; Kirkensgaard, Jacob J K; Mortensen, Kell; Arenz, Matthias

2013-03-14

A colloidal synthesis approach is presented that allows systematic studies of the properties of supported proton exchange membrane fuel cell (PEMFC) catalysts. The applied synthesis route is based on the preparation of monodisperse nanoparticles in the absence of strong binding organic stabilizing agents. No temperature post-treatment of the catalyst is required rendering the synthesis route ideally suitable for comparative studies. We report work concerning a series of catalysts based on the same colloidal Pt nanoparticle (NP) suspension, but with different high surface area (HSA) carbon supports. It is shown that for the prepared catalysts the carbon support has no catalytic co-function, but carbon pre-treatment leads to enhanced sticking of the Pt NPs on the support. An unwanted side effect, however, is NP agglomeration during synthesis. By contrast, enhanced NP sticking without agglomeration can be accomplished by the addition of an ionomer to the NP suspension. The catalytic activity of the prepared catalysts for the oxygen reduction reaction is comparable to industrial catalysts and no influence of the particle size is found in the range of 2-5 nm.

Tracer diffusion in colloidal suspensions under dilute and crowded conditions with hydrodynamic interactions

DEFF Research Database (Denmark)

Tomilov, A.; Videcoq, A.; Chartier, T.

2012-01-01

We consider tracer diffusion in colloidal suspensions under solid loading conditions, where hydrodynamic interactions play an important role. To this end, we carry out computer simulations based on the hybrid stochastic rotation dynamics-molecular dynamics (SRD-MD) technique. Many details of the ...... that hydrodynamic interactions are correctly included within the SRD-MD technique. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4731661]...

Stability of colloidal silver nanoparticles trapped in lipid bilayer: effect of lecithin concentration and applied temperature

NARCIS (Netherlands)

Barani, H.; Montazer, M.; Braun, H.G.; Dutschk, Victoria

2014-01-01

The use of silver nanoparticle on various substrates has been widespread because of its good antibacterial properties that directly depend on the stability of the silver nanoparticles in a colloidal suspension. In this study, the colloidal solutions of the silver nanoparticles were synthesised by a

Experimental data and theoretical predictions for the rate of electrophoretic clarification of colloidal suspensions

Energy Technology Data Exchange (ETDEWEB)

Johnson, T.J.; Davis, E.J.

2000-05-01

An experimental and theoretical investigation of the electrophoretic clarification rate of colloidal suspensions was conducted. The suspensions included a coal-washing effluent and a model system of TiO{sub 2} particles. A parametric study of TiO{sub 2} suspensions was performed to validate and analysis of the electrophoretic motion of the clarification front formed between a clear zone and the suspension. To measure the electric field strength needed in the prediction of the location of the front, a moveable probe and salt bridge were connected to a reference electrode. Using the measured electric field strengths, it was found that the numerical solution to the unit cell electrophoresis model agrees with the measured clarification rates. For suspensions with moderately thick electric double layers and high particle volume fractions the deviations from classical Smoluchowski theory are substantial, and the numerical analysis is in somewhat better agreement with the data than a prior solution of the problem. The numerical model reduces to the predictions of previous theories as the thickness of the electric double layer decreases, and it is in good agreement with the clarification rate measured for a coal-washing effluent suspension with thin electric double layers.

Rheological State Diagrams for Rough Colloids in Shear Flow.

Science.gov (United States)

Hsiao, Lilian C; Jamali, Safa; Glynos, Emmanouil; Green, Peter F; Larson, Ronald G; Solomon, Michael J

2017-10-13

To assess the role of particle roughness in the rheological phenomena of concentrated colloidal suspensions, we develop model colloids with varying surface roughness length scales up to 10% of the particle radius. Increasing surface roughness shifts the onset of both shear thickening and dilatancy towards lower volume fractions and critical stresses. Experimental data are supported by computer simulations of spherical colloids with adjustable friction coefficients, demonstrating that a reduction in the onset stress of thickening and a sign change in the first normal stresses occur when friction competes with lubrication. In the quasi-Newtonian flow regime, roughness increases the effective packing fraction of colloids. As the shear stress increases and suspensions of rough colloids approach jamming, the first normal stresses switch signs and the critical force required to generate contacts is drastically reduced. This is likely a signature of the lubrication films giving way to roughness-induced tangential interactions that bring about load-bearing contacts in the compression axis of flow.

Rheological State Diagrams for Rough Colloids in Shear Flow

Science.gov (United States)

Hsiao, Lilian C.; Jamali, Safa; Glynos, Emmanouil; Green, Peter F.; Larson, Ronald G.; Solomon, Michael J.

2017-10-01

To assess the role of particle roughness in the rheological phenomena of concentrated colloidal suspensions, we develop model colloids with varying surface roughness length scales up to 10% of the particle radius. Increasing surface roughness shifts the onset of both shear thickening and dilatancy towards lower volume fractions and critical stresses. Experimental data are supported by computer simulations of spherical colloids with adjustable friction coefficients, demonstrating that a reduction in the onset stress of thickening and a sign change in the first normal stresses occur when friction competes with lubrication. In the quasi-Newtonian flow regime, roughness increases the effective packing fraction of colloids. As the shear stress increases and suspensions of rough colloids approach jamming, the first normal stresses switch signs and the critical force required to generate contacts is drastically reduced. This is likely a signature of the lubrication films giving way to roughness-induced tangential interactions that bring about load-bearing contacts in the compression axis of flow.

Investigating high-concentration monoclonal antibody powder suspension in nonaqueous suspension vehicles for subcutaneous injection.

Science.gov (United States)

Bowen, Mayumi; Armstrong, Nick; Maa, Yuh-Fun

2012-12-01

Developing high-concentration monoclonal antibody (mAb) liquid formulations for subcutaneous (s.c.) administration is challenging because increased viscosity makes injection difficult. To overcome this obstacle, we investigated a nonaqueous powder suspension approach. Three IgG1 mAbs were spray dried and suspended at different concentrations in Miglyol® 840, benzyl benzoate, or ethyl lactate. Suspensions were characterized for viscosity, particle size, and syringeability; physical stability was visually inspected. Suspensions generally outperformed liquid solutions for injectability despite higher viscosity at the same mAb concentrations. Powder formulations and properties had little effect on viscosity or injectability. Ethyl lactate suspensions had lowest viscosity (Miglyol® 840 improved overall performance in high mAb concentration suspensions. This study demonstrated the viability of high mAb concentration (>300 mg/mL) in suspension formulations for s.c. administration. Copyright © 2012 Wiley Periodicals, Inc.

Brownian dynamics simulations of an order-disorder transition in sheared sterically stabilized colloidal suspensions

International Nuclear Information System (INIS)

Rigos, A.A.; Wilemski, G.

1992-01-01

The shear thinning behavior of a sterically stabilized nonaqueous colloidal suspension was investigated using nonequilibrium Brownian dynamics simulations of systems with 108 and 256 particles. At a volume fraction of 0.4, the suspension is thixotropic: it has a reversible shear thinning transition from a disordered state to an ordered, lamellar state with triangularly packed strings of particles. The time scale for the transition is set by the free particle diffusion constant. For the smaller system, the transition occurs gradually with increasing shear rate. For the larger system, the transition is sharp and discontinuous shear thinning is found. 34 refs., 9 figs., 1 tab

Colloid-Associated Radionuclide Concentration Limits: ANL

International Nuclear Information System (INIS)

Mertz, C.

2000-01-01

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

Characteristics of colloids generated during the corrosion of nuclear waste glasses in groundwater

International Nuclear Information System (INIS)

Feng, X.; Buck, E.C.; Mertz, C.; Bates, J.K.; Cunnane, J.C.; Chaiko, D.

1993-10-01

Aqueous colloidal suspensions were generated by reacting nuclear waste glasses with groundwater at 90 degrees C at different ratios of the glass surface area to solution volume (S/V). The colloids have been characterized in terms of size, charge, identity, and stability with respect to salt concentration, pH, and time, by examination using dynamic light scattering, electrophoretic mobility, and transmission electron microscopy. The colloids are predominately produced by precipitation from solution, possibly with contribution from reacted layers that have spallated from the glass. These colloids are silicon-rich minerals. The colloidal suspensions agglomerate when the salinity of the solutions increase. The following implications for modeling the colloidal transport of contaminants have been derived from this study: (1) The sources of the colloids are not only solubility-limited real colloids and the pseudo colloids formed by adsorption of radionuclides onto a groundwater colloid, but also from the spalled surface layers of reacted waste glasses. (2) In a repository, the local environment is likely to be glass-reaction dominated and the salt concentration is likely to be high, leading to rapid colloid agglomeration and settling; thus, colloid transport may be insignificant. (3) If large volumes of groundwater contact the glass reaction site, the precipitated colloids may become resuspended, and colloid transport may become important. (4) Under most conditions, the colloids are negatively charged and will deposit readily on positively charged surfaces. Negatively charged surfaces will, in general, facilitate colloid stability and transport

Experimental data and theoretical predictions of the rate of electrophoretic clarification of colloidal suspensions

Energy Technology Data Exchange (ETDEWEB)

Johnson, T.J.; Davis, E.J. [University of Washington, Seattle, WA (USA). Dept. of Chemical Engineering

2000-05-01

An experimental and theoretical investigation of the electrophoretic clarification rate of colloidal suspensions was conducted. The suspensions included a coal-washing effluent and a model system of TiO{sub 2} particles. A parametric study of TiO{sub 2} suspensions was performed to validate an analysis of the electrophoretic motion of the clarification front formed between a clear zone and the suspension. To measure the electric field strength needed in the prediction of the location of the front, a moveable probe and salt bridge were connected to a reference electrode. Using the measured electric field strength, it was found that the numerical solution to the unit cell electrophoresis model agrees with the measured clarification rates. For suspensions with moderately thick electric double layers and high particle volume fractions the deviations from classical Smoluchowski theory are substantial, and the numerical analysis is in somewhat better agreement with the data than a prior solution of the problem. The numerical model reduces to the predictions of previous theories as the thickness of the electric double layer decreases, and it is in good agreement with the clarification rate measured for a coal-washing effluent suspension with thin electric double layers. 21 refs., 8 figs., 4 tabs.

Colloidal organization

CERN Document Server

Okubo, Tsuneo

2015-01-01

Colloidal Organization presents a chemical and physical study on colloidal organization phenomena including equilibrium systems such as colloidal crystallization, drying patterns as an example of a dissipative system and similar sized aggregation. This book outlines the fundamental science behind colloid and surface chemistry and the findings from the author's own laboratory. The text goes on to discuss in-depth colloidal crystallization, gel crystallization, drying dissipative structures of solutions, suspensions and gels, and similar-sized aggregates from nanosized particles. Special emphas

Modelling the evaporation of thin films of colloidal suspensions using dynamical density functional theory

Energy Technology Data Exchange (ETDEWEB)

Robbins, M J; Archer, A J; Thiele, U [Department of Mathematical Sciences, Loughborough University, Leicestershire LE11 3TU (United Kingdom)

2011-10-19

Recent experiments have shown that various structures may be formed during the evaporative dewetting of thin films of colloidal suspensions. Nanoparticle deposits of strongly branched 'flower-like', labyrinthine and network structures are observed. They are caused by the different transport processes and the rich phase behaviour of the system. We develop a model for the system, based on a dynamical density functional theory, which reproduces these structures. The model is employed to determine the influences of the solvent evaporation and of the diffusion of the colloidal particles and of the liquid over the surface. Finally, we investigate the conditions needed for 'liquid-particle' phase separation to occur and discuss its effect on the self-organized nanostructures. (paper)

Dynamics of highly polydisperse colloidal suspensions as a model system for bacterial cytoplasm.

Science.gov (United States)

Hwang, Jiye; Kim, Jeongmin; Sung, Bong June

2016-08-01

There are various kinds of macromolecules in bacterial cell cytoplasm. The size polydispersity of the macromolecules is so significant that the crystallization and the phase separation could be suppressed, thus stabilizing the liquid state of bacterial cytoplasm. On the other hand, recent experiments suggested that the macromolecules in bacterial cytoplasm should exhibit glassy dynamics, which should be also affected significantly by the size polydispersity of the macromolecules. In this work, we investigate the anomalous and slow dynamics of highly polydisperse colloidal suspensions, of which size distribution is chosen to mimic Escherichia coli cytoplasm. We find from our Langevin dynamics simulations that the diffusion coefficient (D_{tot}) and the displacement distribution functions (P(r,t)) averaged over all colloids of different sizes do not show anomalous and glassy dynamic behaviors until the system volume fraction ϕ is increased up to 0.82. This indicates that the intrinsic polydispersity of bacterial cytoplasm should suppress the glass transition and help maintain the liquid state of the cytoplasm. On the other hand, colloids of each kind show totally different dynamic behaviors depending on their size. The dynamics of colloids of different size becomes non-Gaussian at a different range of ϕ, which suggests that a multistep glass transition should occur. The largest colloids undergo the glass transition at ϕ=0.65, while the glass transition does not occur for smaller colloids in our simulations even at the highest value of ϕ. We also investigate the distribution (P(θ,t)) of the relative angles of displacement for macromolecules and find that macromolecules undergo directionally correlated motions in a sufficiently dense system.

How Confinement-Induced Structures Alter the Contribution of Hydrodynamic and Short-Ranged Repulsion Forces to the Viscosity of Colloidal Suspensions

Directory of Open Access Journals (Sweden)

Meera Ramaswamy

2017-10-01

Full Text Available Confined systems ranging from the atomic to the granular are ubiquitous in nature. Experiments and simulations of such atomic and granular systems have shown a complex relationship between the microstructural arrangements under confinement, the short-ranged particle stresses, and flow fields. Understanding the same correlation between structure and rheology in the colloidal regime is important due to the significance of such suspensions in industrial applications. Moreover, colloidal suspensions exhibit a wide range of structures under confinement that could considerably modify such force balances and the resulting viscosity. Here, we use a combination of experiments and simulations to elucidate how confinement-induced structures alter the relative contributions of hydrodynamic and short-range repulsive forces to produce up to a tenfold change in the viscosity. In the experiments we use a custom-built confocal rheoscope to image the particle configurations of a colloidal suspension while simultaneously measuring its stress response. We find that as the gap decreases below 15 particle diameters, the viscosity first decreases from its bulk value, shows fluctuations with the gap, and then sharply increases for gaps below 3 particle diameters. These trends in the viscosity are shown to strongly correlate with the suspension microstructure. Further, we compare our experimental results to those from two different simulations techniques, which enables us to determine the relative contributions of hydrodynamic and short-range repulsive stresses to the suspension rheology. The first method uses the lubrication approximation to find the hydrodynamic stress and includes a short-range repulsive force between the particles while the second is a Stokesian dynamics simulation that calculates the full hydrodynamic stress in the suspension. We find that the decrease in the viscosity at moderate confinements has a significant contribution from both the

Growth kinetics of tin oxide nanocrystals in colloidal suspensions under hydrothermal conditions

International Nuclear Information System (INIS)

Lee, Eduardo J.H.; Ribeiro, Caue; Longo, Elson; Leite, Edson R.

2006-01-01

Colloidal suspensions of tin oxide nanocrystals were synthesized at room temperature by the hydrolysis reaction of tin chloride (II), in an ethanolic solution. The coarsening kinetics of such nanocrystals was studied by submitting the as-prepared suspensions to hydrothermal treatments at temperatures of 100, 150 and 200 deg. C for periods between 60 and 12,000 min. Transmission electron microscopy (TEM) was used to characterize the samples (i.e. distribution of nanocrystal size, average particle radius and morphology). The results show that the usual Ostwald ripening coarsening mechanism does not fit well the experimental data, which is an indicative that this process is not significant for SnO 2 nanocrystals, in the studied experimental conditions. The morphology evolution of the nanocrystals upon hydrothermal treatment indicates that growth by oriented attachment (OA) should be significant. A kinetic model that describes OA growth is successfully applied to fit the data

Liquid crystalline phases in suspensions of pigments in non-polar solvents

Science.gov (United States)

Klein, Susanne; Richardson, Robert M.; Eremin, Alexey

We will discuss colloid suspensions of pigments and compare their electro-optic properties with those of traditional dyed low molecular weight liquid crystal systems. There are several potential advantages of colloidal suspensions over low molecular weight liquid crystal systems: a very high contrast because of the high orientational order parameter of suspensions of rod shaped nano-particles, the excellent light fastness of pigments as compared to dyes and high colour saturations resulting from the high loading of the colour stuff. Although a weak `single-particle' electro-optic response can be observed in dilute suspensions, the response is very much enhanced when the concentration of the particles is sufficient to lead to a nematic phase. Excellent stability of suspensions is beneficial for experimental observation and reproducibility, but it is a fundamental necessity for display applications. We therefore discuss a method to achieve long term stability of dispersed pigments and the reasons for its success. Small angle X-ray scattering was used to determine the orientational order parameter of the suspensions as a function of concentration and the dynamic response to an applied electric field. Optical properties were investigated for a wide range of pigment concentrations. Electro-optical phenomena, such as field-induced birefringence and switching, were characterised. In addition, mixtures of pigment suspensions with small amounts of ferrofluids show promise as future magneto-optical materials.

Waste Form and Indrift Colloids-Associated Radionuclide Concentrations: Abstraction and Summary

International Nuclear Information System (INIS)

Aguilar, R.

2003-01-01

This Model Report describes the analysis and abstractions of the colloids process model for the waste form and engineered barrier system components of the total system performance assessment calculations to be performed with the Total System Performance Assessment-License Application model. Included in this report is a description of (1) the types and concentrations of colloids that could be generated in the waste package from degradation of waste forms and the corrosion of the waste package materials, (2) types and concentrations of colloids produced from the steel components of the repository and their potential role in radionuclide transport, and (3) types and concentrations of colloids present in natural waters in the vicinity of Yucca Mountain. Additionally, attachment/detachment characteristics and mechanisms of colloids anticipated in the repository are addressed and discussed. The abstraction of the process model is intended to capture the most important characteristics of radionuclide-colloid behavior for use in predicting the potential impact of colloid-facilitated radionuclide transport on repository performance

Waste Form and Indrift Colloids-Associated Radionuclide Concentrations: Abstraction and Summary

Energy Technology Data Exchange (ETDEWEB)

R. Aguilar

2003-06-24

This Model Report describes the analysis and abstractions of the colloids process model for the waste form and engineered barrier system components of the total system performance assessment calculations to be performed with the Total System Performance Assessment-License Application model. Included in this report is a description of (1) the types and concentrations of colloids that could be generated in the waste package from degradation of waste forms and the corrosion of the waste package materials, (2) types and concentrations of colloids produced from the steel components of the repository and their potential role in radionuclide transport, and (3) types and concentrations of colloids present in natural waters in the vicinity of Yucca Mountain. Additionally, attachment/detachment characteristics and mechanisms of colloids anticipated in the repository are addressed and discussed. The abstraction of the process model is intended to capture the most important characteristics of radionuclide-colloid behavior for use in predicting the potential impact of colloid-facilitated radionuclide transport on repository performance.

Fracture in Kaolinite clay suspensions

Science.gov (United States)

Kosgodagan Acharige, Sebastien; Jerolmack, Douglas J.; Arratia, Paulo E.

2017-11-01

Clay minerals are involved in many natural (landslides, river channels) and industrial processes (ceramics, cosmetics, oil recovery). They are plate shaped charged colloids and exhibit different flow properties than simpler colloids when suspended in a liquid such as thixotropy and shear-banding. kaolinite platelets are non-swelling, meaning that the stacks formed by the platelets do not have water layers, and thus the suspension does not have a sol-gel transition. However, it has been shown that kaolinite suspensions possesses a non-zero yield stress even at low concentrations, indicating that the particles arrange themselves in a structure through attractive interactions. Here, we experimentally investigate the sedimentation of kaolinite suspensions in a Hele-Shaw cell. The sedimentation of these dilute suspensions can display solid behavior like fracture, revealed in cross-polarized light, which is linked to the failure of the weakly-bonded structure (typical yield stress 10-2 Pa). By changing the interaction potential of the particles (by sonication or introducing salts), we show through these sedimentation experiments, how the fracture pattern can be avoided. Research was sponsored by the Army Research Laboratory and was accomplished under Grant Number 569074.

Hybrid electrokinetics for separation, mixing, and concentration of colloidal particles

International Nuclear Information System (INIS)

Sin, Mandy L Y; Shimabukuro, Yusuke; Wong, Pak Kin

2009-01-01

The advent of nanotechnology has facilitated the preparation of colloidal particles with adjustable sizes and the control of their size-dependent properties. Physical manipulation, such as separation, mixing, and concentration, of these colloidal particles represents an essential step for fully utilizing their potential in a wide spectrum of nanotechnology applications. In this study, we investigate hybrid electrokinetics, the combination of dielectrophoresis and electrohydrodynamics, for active manipulation of colloidal particles ranging from nanometers to micrometers in size. A concentric electrode configuration, which is optimized for generating electrohydrodynamic flow, has been designed to elucidate the effectiveness of hybrid electrokinetics and define the operating regimes for different microfluidic operations. The results indicate that the relative importance of electrohydrodynamics increases with decreasing particle size as predicted by a scaling analysis and that electrohydrodynamics is pivotal for manipulating nanoscale particles. Using the concentric electrodes, we demonstrate separation, mixing, and concentration of colloidal particles by adjusting the relative strengths of different electrokinetic phenomena. The effectiveness of hybrid electrokinetics indicates its potential to serve as a generic technique for active manipulation of colloidal particles in various nanotechnology applications.

Modified Mason number for charged paramagnetic colloidal suspensions

Science.gov (United States)

Du, Di; Hilou, Elaa; Biswal, Sibani Lisa

2016-06-01

The dynamics of magnetorheological fluids have typically been described by the Mason number, a governing parameter defined as the ratio between viscous and magnetic forces in the fluid. For most experimental suspensions of magnetic particles, surface forces, such as steric and electrostatic interactions, can significantly influence the dynamics. Here we propose a theory of a modified Mason number that accounts for surface forces and show that this modified Mason number is a function of interparticle distance. We demonstrate that this modified Mason number is accurate in describing the dynamics of a rotating pair of paramagnetic colloids of identical or mismatched sizes in either high or low salt solutions. The modified Mason number is confirmed to be pseudoconstant for particle pairs and particle chains undergoing a stable-metastable transition during rotation. The interparticle distance term can be calculated using theory or can be measured experimentally. This modified Mason number is more applicable to magnetorheological systems where surface forces are not negligible.

Manipulating colloids with charges and electric fields

Science.gov (United States)

Leunissen, M. E.

2007-02-01

This thesis presents the results of experimental investigations on a variety of colloidal suspensions. Colloidal particles are at least a hundred times larger than atoms or molecules, but suspended in a liquid they display the same phase behavior, including fluid and crystalline phases. Due to their relatively large size, colloids are much easier to investigate and manipulate, though. This makes them excellent condensed matter model systems. With this in mind, we studied micrometer-sized perspex (‘PMMA’) spheres, labeled with a fluorescent dye for high-resolution confocal microscopy imaging, and suspended in a low-polar mixture of the organic solvents cyclohexyl bromide and cis-decalin. This system offered us the flexibility to change the interactions between the particles from ‘hard-sphere-like’ to long-ranged repulsive (between like-charged particles), long-ranged attractive (between oppositely charged particles) and dipolar (in an electric field). We investigated the phase behavior of our suspensions as a function of the particle concentration, the ionic strength of the solvent and the particles’ charges. In this way, we obtained new insight in the freezing and melting behavior of like-charged and oppositely charged colloids. Interestingly, we found that the latter can readily form large crystals, thus defying the common belief that plus-minus interactions inevitably lead to aggregation. Moreover, we demonstrated that these systems can serve as a reliable model system for classical ionic matter (‘salts’), and that opposite-charge interactions can greatly facilitate the self-assembly of new structures with special properties for applications. On a slightly different note, we also studied electrostatic effects in mixtures of the cyclohexyl bromide solvent and water, both with and without colloidal particles present. This provided new insight in the stabilization mechanisms of oil-water emulsions and gave us control over the self-assembly of various

A radiometric method for the characterization of particulate processes in colloidal suspensions. II

International Nuclear Information System (INIS)

Subotic, B.

1979-01-01

A radiometric method for the characterization of particulate processes is verified using stable hydrosols of silver iodide. Silver iodide hydrosols satisfy the conditions required for the applications of the proposed method. Comparison shows that the values for the change of particle size measured in silver iodide hydrosols by the proposed method are in excellent agreement with the values obtained by other methods on the same systems (electron microscopy, sedimentation analysis, light scattering). This shows that the proposed method is suitable for the characterization of particulate processes in colloidal suspensions. (Auth.

Nonlinear response of dense colloidal suspensions under oscillatory shear: mode-coupling theory and Fourier transform rheology experiments.

Science.gov (United States)

Brader, J M; Siebenbürger, M; Ballauff, M; Reinheimer, K; Wilhelm, M; Frey, S J; Weysser, F; Fuchs, M

2010-12-01

Using a combination of theory, experiment, and simulation we investigate the nonlinear response of dense colloidal suspensions to large amplitude oscillatory shear flow. The time-dependent stress response is calculated using a recently developed schematic mode-coupling-type theory describing colloidal suspensions under externally applied flow. For finite strain amplitudes the theory generates a nonlinear response, characterized by significant higher harmonic contributions. An important feature of the theory is the prediction of an ideal glass transition at sufficiently strong coupling, which is accompanied by the discontinuous appearance of a dynamic yield stress. For the oscillatory shear flow under consideration we find that the yield stress plays an important role in determining the nonlinearity of the time-dependent stress response. Our theoretical findings are strongly supported by both large amplitude oscillatory experiments (with Fourier transform rheology analysis) on suspensions of thermosensitive core-shell particles dispersed in water and Brownian dynamics simulations performed on a two-dimensional binary hard-disk mixture. In particular, theory predicts nontrivial values of the exponents governing the final decay of the storage and loss moduli as a function of strain amplitude which are in good agreement with both simulation and experiment. A consistent set of parameters in the presented schematic model achieves to jointly describe linear moduli, nonlinear flow curves, and large amplitude oscillatory spectroscopy.

Au, Ag and Au:Ag colloidal nanoparticles synthesized by pulsed laser ablation as SERS substrates

Directory of Open Access Journals (Sweden)

M. Vinod

2014-12-01

Full Text Available Chemically pure colloidal suspensions of gold and silver nanoparticles were synthesized using pulsed laser ablation. The dependence of laser fluence on the surface plasmon characteristics of the nanoparticles was investigated. Au:Ag colloidal suspensions were prepared by mixing highly monodisperse Au and Ag nanocolloids. The plasmon band of these mixtures was found to be highly sensitive to Au:Ag concentration ratio and wavelength of the laser beam used in the ablation process. The Au:Ag mixture consists of almost spherical shaped nanostructures with a tendency to join with adjacent ones. The surface enhanced Raman scattering activity of the Au, Ag and Au:Ag colloidal suspensions was tested using crystal violet as probe molecules. Enhancement in Raman signal obtained with Au:Ag substrates was found to be promising and strongly depends on its plasmon characteristics.

Low frequency dielectric relaxation processes and ionic conductivity of montmorillonite clay nanoparticles colloidal suspension in poly(vinyl pyrrolidone−ethylene glycol blends

Directory of Open Access Journals (Sweden)

2008-11-01

Full Text Available The dielectric dispersion behaviour of montmorillonite (MMT clay nanoparticles colloidal suspension in poly(vinyl pyrrolidone-ethylene glycol (PVP-EG blends were investigated over the frequency range 20 Hz to 1 MHz at 30°C. The 0, 1, 2, 3, 5 and 10 wt% MMT clay concentration of the weight of total solute (MMT+PVP were prepared in PVP-EG blends using EG as solvent. The complex relative dielectric function, alternating current (ac electrical conductivity, electric modulus and impedance spectra of these materials show the relaxation processes corresponding to the micro-Brownian motion of PVP chain, ion conduction and electrode polarization phenomena. The real part of ac conductivity spectra of these materials obeys Jonscher power law σ′(ω =σdc + Aωn in upper frequency end of the measurement, whereas dispersion in lower frequency end confirms the presence of electrode polarization effect. It was observed that the increase of clay concentration in the PVP-EG blends significantly increases the ac conductivity values, and simultaneously reduces the ionic conductivity relaxation time and electric double layer relaxation time, which suggests that PVP segmental dynamics and ionic motion are strongly coupled. The intercalation of EG structures in clay galleries and exfoliation of clay sheets by adsorption of PVP-EG structures on clay surfaces are discussed by considering the hydrogen bonding interactions between the hydroxyl group (–OH of EG molecules, carbonyl group (C=O of PVP monomer units, and the hydroxylated aluminate surfaces of the MMT clay particles. Results suggest that the colloidal suspension of MMT clay nano particles in the PVP-EG blends provide a convenient way to obtain an electrolyte solution with tailored electrical conduction properties.

Colloidal approach to dispersion and enhanced deaggregation of aqueous ferrite suspensions

Science.gov (United States)

Mandanas, Michael Patrick M.

The role of solution and surface chemistry on deaggregation of calcined ferrites during attrition (stirred-media) milling of aqueous suspensions were investigated. Suspensions of commercially calcined Fe2O 3 powder (d50 ˜ 5.0 mum) were milled at different solid loadings and suspension pH. The drift of suspension pH, from pH 2.5 to pH 7.0, during solid loading experiments accounted for the observed reagglomeration with milling time. The observed deaggregation rates during pH stat milling, in the acidic region, can be related to (i) elevated solubility and (ii) enhanced dispersion via surface charge. Proton adsorption density during pH stat milling at different pH values is also comparable to existing potentiometric titration plots and can be related to deaggregation rates. A passivation-dispersion approach for dispersing manganese zinc ferrite (MnxZn(1 - x)Fe2O4) powder is presented. Addition of oxalic acid can help control dissolution reactions from particle surfaces and is subsequently dispersed with polyethyleneimine (PEI). Fully dissociated oxalic acid (pK1 = 1.2, pK2 = 4.3) solutions reacted with MnxZn(1 - x)Fe 2O4 leads to the formation of a uniform negative charge on the particle surface, resulting from the sparingly soluble salt formed on the surface. The resulting rheological data for passivation/dispersion of relatively high solid MnxZn(1 - x)Fe2O 4 suspensions (˜80 w/o, (˜40 v/o)) demonstrate improved colloid stability with improved rheological properties. Using the passivation dispersion scheme developed, deaggregation of commercially calcined MnxZn(1 - x)Fe2O4 powders during attrition milling was investigated. Reagglomeration is apparent when using a typical treatment, 2 w/w of a sulfonated based naphthalene condensate, during deaggregation of the calcined MnxZn(1 - x)Fe 2O4. However, is not observed for select oxalate/PEI treatments. The determined ideal treatment is 2 w/w oxalate and 3 w/w PEI based on the particle size and rheological

Yielding and flow of sheared colloidal glasses

International Nuclear Information System (INIS)

Petekidis, G; Vlassopoulos, D; Pusey, P N

2004-01-01

We have studied some of the rheological properties of suspensions of hard-sphere colloids with particular reference to behaviour near the concentration of the glass transition. First we monitored the strain on the samples during and after a transient step stress. We find that, at all values of applied step stress, colloidal glasses show a rapid, apparently elastic, recovery of strain after the stress is removed. This recovery is found even in samples which have flowed significantly during stressing. We attribute this behaviour to 'cage elasticity', the recovery of the stress-induced distorted environment of any particle to a more isotropic state when the stress is removed. Second, we monitored the stress as the strain rate dot γ of flowing samples was slowly decreased. Suspensions which are glassy at rest show a stress which becomes independent of dot γ as dot γ →0. This limiting stress can be interpreted as the yield stress of the glass and agrees well both with the yield stress deduced from the step stress and recovery measurements and that predicted by a recent mode coupling theory of sheared suspensions. Thus, the behaviours under steady shearing and transient step stress both support the idea that colloidal glasses have a finite yield stress. We note however that the samples do exhibit a slow accumulation of strain due to creep at stresses below the yield stress

Interactions in YBa2Cu3O7-x aqueous suspensions

International Nuclear Information System (INIS)

Dusoulier, Laurent; Cloots, Rudi; Vertruyen, Benedicte; Garcia-Fierro, Jose L.; Moreno, Rodrigo; Ferrari, Begona

2009-01-01

Surface charging mechanism of YBa 2 Cu 3 O 7-x (YBCO) particles in water has been investigated in order to understand their colloidal behaviour and stabilise concentrated suspensions. A broad study relating the suspension parameters (pH and zeta potential) vs. the conditions of the suspension performance (atmosphere and time) has been shown and discussed. The zeta potential values remain positive in all the pH range for the highest powder concentration studied (10 g l -1 ), evidencing a large influence of the solid content in the particle charge. The chemistry of YBa 2 Cu 3 O 7-x in water has been studied through the chemical analysis of the supernatant by inductively coupled plasma (ICP), and the surface analysis of the particles by X-ray diffraction analysis (XRD) and X-ray photoelectron spectroscopy (XPS). The presence of BaCO 3 , CuO, and the hydrolysed Ba species, such as Ba(OH) 2 and Ba(OH) + , at the particles surface has been evaluated as a function of the powder concentration. Based on these analyses, the dependence of the colloidal behaviour of YBCO on the presence of Ba soluble species has been determined. A stabilisation mechanism for YBCO particles in aqueous suspension focus on the powders deleterious minimization was proposed.

Elastic Modulus at High Frequency of Polymerically Stabilized Suspensions

NARCIS (Netherlands)

Nommensen, P.A.; Duits, Michael H.G.; van den Ende, Henricus T.M.; Mellema, J.

2000-01-01

The elastic moduli of polymerically stabilized suspensions consisting of colloidal silica particles coated with endgrafted PDMS (Mn = 80 000) in heptane, were measured as a function of concentration. And the elastic modulus at high frequency G'.. was quantitatively described by model calculations

Correlated particle dynamics in concentrated quasi-two-dimensional suspensions

International Nuclear Information System (INIS)

Diamant, H; Cui, B; Lin, B; Rice, S A

2005-01-01

We investigate theoretically and experimentally how the hydrodynamically correlated lateral motion of particles in a suspension confined between two surfaces is affected by the suspension concentration. Despite the long range of the correlations (decaying as 1/r 2 with the inter-particle distance r), the concentration effect is present only at short inter-particle distances for which the static pair correlation is nonuniform. This is in sharp contrast with the effect of hydrodynamic screening in unconfined suspensions, where increasing the concentration changes the prefactor of the large-distance correlation

Shear-induced changes of electrical conductivity in suspensions

Energy Technology Data Exchange (ETDEWEB)

Crawshaw, John; Meeten, Gerald [Schlumberger Cambridge Research, Cambridge (United Kingdom)

2006-12-15

The effect of shear on electrical conductivity (rheo-conduction) is studied to give information about particle behaviour in suspensions. Past work is reviewed, and expressions are derived for the rheo-conduction of a suspension of nonconducting spheroids in a conducting matrix for current flow, parallel and normal to the suspension flow direction. A simple apparatus to study rheo-conduction in pipe flow is described, and measurements of steady and time-dependent effects are reported for various suspensions of colloidal particles. Suspensions of anisometric rod- and platelike particles at low concentrations showed rheo-conductive changes of sign, magnitude and relaxation that were consistent with the particle shape, concentration and interactions. The rheo-conductive response decreased with increasing volume fraction for platelike kaolinite particles, attributed to orientational jamming. Spherical latex particles gave unexpected rheo-conductive changes consistent with shear disruption of a conductive network of particles. It is concluded that rheo-conduction measurements are a useful adjunct to conventional rheometry. (orig.)

Microscopic dynamics of binary mixtures and quasi-colloidal systems

International Nuclear Information System (INIS)

Smorenburg, H.E.

1996-01-01

In the study on the title subject two questions are addressed. One is whether the microscopic dynamics of binary mixtures and quasi-colloidal systems can be understood theoretically with kinetic theories for equivalent hard sphere mixtures. The other question that arises is whether the similarity in the dynamics of dense simple fluids and concentrated colloidal suspensions also holds for binary mixtures and quasi-colloidal systems. To answer these questions, we have investigated a number of binary gas mixtures and quasi-colloidal system with different diameter ratios and concentrations. We obtain the experimental dynamic structure factors S expt (κ,ω) of the samples from inelastic neutron scattering. We compare S expt (κ,ω) with the dynamic structure S HS (κ,ω) of an equivalent hard sphere fluid, that we calculate with the Enskog theory. In chapter 2, 3 and 4 we study dense He-Ar gas mixtures (diameter ratio R=1.4, and mass ratio M=10) at low and high Ar concentrations. Experiment and kinetic theory are in good agreement. In chapter 5 we study dilute quasi-colloidal suspensions of fullerene C60 molecules dissolved in liquid CS2. The diameter ratio R=2.2 is larger than in previous experiments while the mass ratio M=9.5 is more or less the same. We obtain the self diffusion coefficient D S of one C60 molecule in CS2 and find D s ≤D SE ≤D E , with D E obtained from kinetic theory and D SE from the Stokes-Einstein description. It appears that both descriptions are relevant but not so accurate. In chapter 6 we study three dense mixtures of neopentane in 40 Ar (diameter ratio R=1.7, mass ratio M=2) at low and high neopentane concentrations. At low concentration, we find a diffusion coefficient of neopentane in Ar, which is in good agreement with kinetic theory and in moderate agreement with the Stokes-Einstein description. At high concentration the collective translational dynamics of neopentane shows a similar behaviour as in dense colloids and simple fluids

Colloidal suspensions hydrodynamic retention mechanisms in model porous media; Mecanismes de retention hydrodynamique de suspensions colloidales en milieux poreux modeles

Energy Technology Data Exchange (ETDEWEB)

Salehi, N

1996-04-19

This study deals with the retention mechanisms of colloidal particles in porous media flows, and the subsequent reduction in permeability in the case of stable and non adsorbing colloids. It combines experimental results and modelling. This study has been realised with stable dispersion of monodispersed carboxylate polystyrene latexes negatively charged injected through negatively charged polycarbonate membranes having mono-sized cylindrical pores. The mean particle diameter is smaller than the mean pore diameter. Both batch and flow experiments in Nuclepore membranes have been done. The results of batch experiments have proved no adsorption of the colloidal latex particles on the surface of the Nuclepore membranes without flow at low salinity. In flow experiments at low particle concentration, only deposition on the upstream side of the membrane have been induced by hydrodynamic forces even for non adsorbing particles without creating any permeability reduction. The retention levels are zero at low and high Peclet numbers with a maximum at intermediate values. Partial plugging was observed at higher colloid concentration even at low salinity without any upstream surface deposition. The modelling of plugging processes is achieved by considering the particle concentration, fluid rate and ratio between the mean pore diameter and the mean particle diameter. This study can be particularly useful in the fields of water treatment and of restoration of lands following radioactive contamination. (author). 96 refs., 99 figs., 29 tabs.

Simulation of shear thickening in attractive colloidal suspensions.

Science.gov (United States)

Pednekar, Sidhant; Chun, Jaehun; Morris, Jeffrey F

2017-03-01

The influence of attractive forces between particles under conditions of large particle volume fraction, ϕ, is addressed using numerical simulations which account for hydrodynamic, Brownian, conservative and frictional contact forces. The focus is on conditions for which a significant increase in the apparent viscosity at small shear rates, and possibly the development of a yield stress, is observed. The high shear rate behavior for Brownian suspensions has been shown in recent work [R. Mari, R. Seto, J. F. Morris and M. M. Denn PNAS, 2015, 112, 15326-15330] to be captured by the inclusion of pairwise forces of two forms, one a contact frictional interaction and the second a repulsive force often found in stabilized colloidal dispersions. Under such conditions, shear thickening is observed when shear stress is comparable to the sum of the Brownian stress, kT/a 3 , and a characteristic stress based on the combination of interparticle force, i.e. σ ∼ F 0 /a 2 with kT the thermal energy, F 0 the repulsive force scale and a the particle radius. At sufficiently large ϕ, this shear thickening can be very abrupt. Here it is shown that when attractive interactions are present with the noted forces, the shear thickening is obscured, as the viscosity shear thins with increasing shear rate, eventually descending from an infinite value (yield stress conditions) to a plateau at large stress; this plateau is at the same level as the large-shear rate viscosity found in the shear thickened state without attractive forces. It is shown that this behavior is consistent with prior observations in shear thickening suspensions modified to be attractive through depletion flocculation [V. Gopalakrishnan and C. F. Zukoski J. Rheol., 2004, 48, 1321-1344]. The contributions of the contact, attractive, and hydrodynamics forces to the bulk stress are presented, as are the contact networks found at different attractive strengths.

Silver carbonate and stability in colloidal silver: A by-product of the electric spark discharge method

International Nuclear Information System (INIS)

Tseng, Kuo-Hsiung; Liao, Chih-Yu; Tien, Der-Chi

2010-01-01

Many methods of producing colloidal silver (CS) include the introduction of surfactants to improve the suspensivity of the silver particles. The electric spark discharge method (ESDM) which involves pulses of direct current being passed through a silver electrode submerged in deionized water has been shown to successfully produce colloidal silver in a stable suspension without the use of chemical additives. A by-product of the electric spark discharge method, a silver ion compound (AgX), is shown to be the cause of the high suspensivity of the silver nanoparticles (AgNPs). The silver ion compound has been identified as Ag 2 CO 3 using X-ray diffraction, and it has been determined that the Ag 2 CO 3 is formed during the electric spark discharge process through a reaction with atmospheric CO 2 . It has been shown that an Ag 2 CO 3 concentration of 10 ppm or more is sufficient to generate a stable suspension of silver particles. Because of the occurrence of Ag 2 CO 3 , the electric spark discharge method can produce stable colloidal silver.

Stability of colloidal silver nanoparticles trapped in lipid bilayer: effect of lecithin concentration and applied temperature.

Science.gov (United States)

Barani, Hossein; Montazer, Majid; Braun, Hans-Georg; Dutschk, Victoria

2014-12-01

The use of silver nanoparticle on various substrates has been widespread because of its good antibacterial properties that directly depend on the stability of the silver nanoparticles in a colloidal suspension. In this study, the colloidal solutions of the silver nanoparticles were synthesised by a simple and safe method by using lecithin as a stabilising agent and their stability was examined at various temperatures. The effect of the lecithin concentrations on the stability of the synthesised silver nanoparticles was examined from 25 to 80°C at 5°C intervals, by recording the changes in the UV-vis absorption spectra, the hydrodynamic diameter and the light scattering intensity of the silver nanoparticles. In addition, the morphology of the synthesised silver nanoparticles was investigated with the low-voltage scanning electron microscopy and transmission electron microscopy. The results indicated that increasing temperature caused different changes in the size of the stabilised and the unstabilised silver nanoparticles. The size of the stabilised silver nanoparticles reduced from 38 to 36 nm during increasing temperature, which confirmed good stability.

Transport coefficients and mechanical response in hard-disk colloidal suspensions

International Nuclear Information System (INIS)

Zhang Bo-Kai; Ma Yu-Qiang; Li Jian; Chen Kang; Tian Wen-De

2016-01-01

We investigate the transport properties and mechanical response of glassy hard disks using nonlinear Langevin equation theory. We derive expressions for the elastic shear modulus and viscosity in two dimensions on the basis of thermal-activated barrier-hopping dynamics and mechanically accelerated motion. Dense hard disks exhibit phenomena such as softening elasticity, shear-thinning of viscosity, and yielding upon deformation, which are qualitatively similar to dense hard-sphere colloidal suspensions in three dimensions. These phenomena can be ascribed to stress-induced “landscape tilting”. Quantitative comparisons of these phenomena between hard disks and hard spheres are presented. Interestingly, we find that the density dependence of yield stress in hard disks is much more significant than in hard spheres. Our work provides a foundation for further generalizing the nonlinear Langevin equation theory to address slow dynamics and rheological behavior in binary or polydisperse mixtures of hard or soft disks. (rapid communication)

Improving the strength of ceramics by controlling the interparticle forces and rheology of the ceramic suspensions

International Nuclear Information System (INIS)

Chou, Yi-Ping

2001-01-01

This thesis describes a study of the modification of the interparticle forces of colloidal ceramic particles in aqueous suspensions in order to improve the microstructural homogeneity, and hence the reliability and mechanical performances, of subsequently formed ceramic compacts. A concentrated stable fine ceramic powder suspension has been shown to be able to generate a higher density of a ceramic product with better mechanical, and also electrical, electrochemical and optical, properties of the ceramic body. This is because in a colloidally stable suspension there are no aggregates and so defect formation, which is responsible for the ceramic body performance below its theoretical maximum, is reduced. In order to achieve this, it is necessary to form a well dispersed ceramic suspension by ensuring the interparticle forces between the particles are repulsive, with as a high a loading with particles as possible. By examining the rheological behaviour and the results of Atomic Force Microscope, the dispersion state of the suspensions and hence the interparticle forces can be analysed. In this study, concentrated ceramic suspensions were made from two kinds of zirconia powders, monoclinic (DK1) and yttria partially stabilised (HSY3) zirconia, in the presence of a dispersant, 4,5-dihydroxy-1,3-benzenedisulfonic acid disodium salt (Tiron), in aqueous system. The optimum dispersant concentrations, where the viscosity and rheological moduli are the entire minimum, for DK1 and HSY3 suspensions, respectively, are 0.625% and 0.1%. The modifications of the interparticle forces were also achieved by pH adjustment and it was found that both of the suspensions at the optimum dispersant concentration were stable over the pH range 7 ∼ 10, which coincide with the results of the electrophoretic mobility measurements. Ceramic compacts have then been made by slip casting the suspensions of different dispersant concentration, followed by firing procedure. Mechanical properties of

[MAXIMUM SINGLE DOSE OF COLLOIDAL SILVER NEGATIVELY AFFECTS ERYTHROPOIESIS IN VITRO].

Science.gov (United States)

Tishevskayal, N V; Zakharovl, Y M; Bolotovl, A A; Arkhipenko, Yu V; Sazontova, T G

2015-01-01

Erythroblastic islets (EI) of rat bone marrow were cultured for 24 h in the presence of silver nanoparticles (1.07 · 10(-4) mg/ml; 1.07 · 10(-3) mg/ml; and 1.07 · 10(-2) mg/mL). The colloidal silver at 1.07 · 10(-3) mg/ml concentration inhibited the formation of new Elby disrupting contacts of bone marrow macrophages with CFU-E (erythropoiesis de novo) by 65.3% (p Colloidal silver nanoparticles suppressed the reconstruction of erythropoiesis and inhibited the formation of new EI by disrupting contacts of CFU-E and central macrophages with matured erythroidal "crown" (erythropoiesis de repeto). The colloidal silver concentration of 1.07 · 10(-3) mg/ml in the culture medium also reduced the number of self-reconstructing EI by 67.5% (p colloidal silver reduced this value by 93.7% (p Silver nanoparticles retarded maturation of erythroid cells at the stage of oxiphylic normoblast denucleation: 1.07 · 10(-3) mg/ml colloidal silver increased the number of mature El by 53% (p colloidal silver in concentration equivalent to the maximum single dose is related to the effect of silver nanoparticles rather than glycerol present in the colloidal suspension.

Measurements of colloid concentrations in the fracture zone, Aespoe Hard Rock Laboratory, Sweden

International Nuclear Information System (INIS)

Ledin, A.; Dueker, A.; Karlsson, Stefan; Allard, B.

1995-06-01

The applicability of light scattering in combination with photon correlation spectroscopy (PCS) for determination of concentration and size distribution of colloidal matter in a deep groundwater was tested in situ and on-line. Well-defined reference colloids of Fe 2 O 3 , Al(OH) 3 , SiO 2 , kaolinite, illite and a high molecular humic acid in aqueous media were used as model substances for calibration of the PCS instrument. The intensity of scattered light was found to be dependent on the composition of the colloids. The colloid concentration in the rather saline groundwater was below the detection limit for the PCS equipment used, which corresponds to a colloid concentration not higher than 0.5 mg/l and probably below 0.1 mg/l according to the measurements on-line and in situ at Aespoe and in comparison to the calibrations performed with reference colloids. The results clearly demonstrated that the stability, concentration and composition of a colloid-size suspended phase in the anoxic groundwater with high content of Fe(II), like the one in Aespoe, is extremely sensitive to exposure to atmospheric conditions during sample handling and preparation. Diffusion of air into the closed measuring cuvette was enough to alter the colloid content significantly within 6 hours. A particle fraction with the size distribution in the range 170-700 nm was formed within 45 min when air was allowed to diffuse into the aqueous phase from the air filled upper part of the cuvette. The corresponding time to generate a significant colloid precipitate was less than 1 min when a stream of air was bubbled through the water samples. The precipitated colloid phase consisted of a mixture of ferric (hydr)oxide and calcium carbonate in all three cases. 53 refs, 8 figs, 2 tabs

Colloid transport in porous media: impact of hyper-saline solutions.

Science.gov (United States)

Magal, Einat; Weisbrod, Noam; Yechieli, Yoseph; Walker, Sharon L; Yakirevich, Alexander

2011-05-01

The transport of colloids suspended in natural saline solutions with a wide range of ionic strengths, up to that of Dead Sea brines (10(0.9) M) was explored. Migration of microspheres through saturated sand columns of different sizes was studied in laboratory experiments and simulated with mathematical models. Colloid transport was found to be related to the solution salinity as expected. The relative concentration of colloids at the columns outlet decreased (after 2-3 pore volumes) as the solution ionic strength increased until a critical value was reached (ionic strength > 10(-1.8) M) and then remained constant above this level of salinity. The colloids were found to be mobile even in the extremely saline brines of the Dead Sea. At such high ionic strength no energetic barrier to colloid attachment was presumed to exist and colloid deposition was expected to be a favorable process. However, even at these salinity levels, colloid attachment was not complete and the transport of ∼ 30% of the colloids through the 30-cm long columns was detected. To further explore the deposition of colloids on sand surfaces in Dead Sea brines, transport was studied using 7-cm long columns through which hundreds of pore volumes were introduced. The resulting breakthrough curves exhibited a bimodal shape whereby the relative concentration (C/C(0)) of colloids at the outlet rose to a value of 0.8, and it remained relatively constant (for the ∼ 18 pore volumes during which the colloid suspension was flushed through the column) and then the relative concentration increased to a value of one. The bimodal nature of the breakthrough suggests different rates of colloid attachment. Colloid transport processes were successfully modeled using the limited entrapment model, which assumes that the colloid attachment rate is dependent on the concentration of the attached colloids. Application of this model provided confirmation of the colloid aggregation and their accelerated attachment during

Aging of a Binary Colloidal Glass

Science.gov (United States)

Lynch, Jennifer M.; Cianci, Gianguido C.; Weeks, Eric R.

2008-03-01

After having undergone a glass transition, a glass is in a non-equilibrium state, and its properties depend on the time elapsed since vitrification. We study this phenomenon, known as aging. In particular, we study a colloidal suspension consisting of micron-sized particles in a liquid --- a good model system for studying the glass transition. In this system, the glass transition is approached by increasing the particle concentration, instead of decreasing the temperature. We observe samples composed of particles of two sizes (d1= 1.0μm and d2= 2.0μm) using fast laser scanning confocal microscopy, which yields real-time, three-dimensional movies deep inside the colloidal glass. We then analyze the trajectories of several thousand particles as the glassy suspension ages. Specifically, we look at how the size, motion and structural organization of the particles relate to the overall aging of the glass. We find that areas richer in small particles are more mobile and therefore contribute more to the structural changes found in aging glasses.

Preparation of dielectrics HR mirrors from colloidal oxide suspensions containing organic polymer binders

International Nuclear Information System (INIS)

Thomas, I.M.

1994-01-01

Colloidal suspensions of oxides have been used to prepare dielectric HR (high reflective) mirrors, specifically for high power fusion case applications, on substrates up to 38 cm square using a meniscus coater. These coatings consist of porous quarterwave layers of alternating high and low refractive index oxides. Silica was used as the low index oxide and AlOOH, ZrO 2 , or HfO 2 as the high index material. Coatings were weak because of low particle-to-particle adhesion. Use of organic polymer binders in the high index component was found to increase strength, thereby improving the laser damage threshold and also reducing the number of layers required for 99% reflection due to increased refractive index

Colloidal stability of silver nanoparticles in biologically relevant conditions

International Nuclear Information System (INIS)

MacCuspie, Robert I.

2011-01-01

Understanding the colloidal stability of nanoparticles (NPs) plays a key role in phenomenological interpretation of toxicological experiments, particularly if single NPs or their aggregates or agglomerates determine the dominant experimental result. This report examines a variety of instrumental techniques for surveying the colloidal stability of aqueous suspensions of silver nanoparticles (AgNPs), including atomic force microscopy, dynamic light scattering, and colorimetry. It was found that colorimetry can adequately determine the concentration of single AgNPs that remained in solution if morphological information about agglomerates is not required. The colloidal stability of AgNPs with various surface capping agents and in various solvents ranging from cell culture media to different electrolytes of several concentrations, and in different pH conditions was determined. It was found that biocompatible bulky capping agents, such as bovine serum albumin or starch, that provided steric colloidal stabilization, as opposed to purely electrostatic stabilization such as with citrate AgNPs, provided better retention of single AgNPs in solution over a variety of conditions for up to 64 h of observation.

Magnetic switching of optical reflectivity in nanomagnet/micromirror suspensions: colloid displays as a potential alternative to liquid crystal displays.

Science.gov (United States)

Bubenhofer, S B; Athanassiou, E K; Grass, R N; Koehler, F M; Rossier, M; Stark, W J

2009-12-02

Two-particle colloids containing nanomagnets and microscale mirrors can be prepared from iron oxide nanoparticles, microscale metal flakes and high-density liquids stabilizing the mirror suspension against sedimentation by matching the constituent's density. The free Brownian rotation of the micromirrors can be magnetically controlled through an anisotropic change in impulse transport arising from impacts of the magnetic nanoparticles onto the anisotropic flakes. The resulting rapid mirror orientation allows large changes in light transmission and switchable optical reflectivity. The preparation of a passive display was conceptually demonstrated through colloid confinement in a planar cavity over an array of individually addressable solenoids and resulted in 4 x 4 digit displays with a reaction time of less than 100 ms.

Probing droplets with biological colloidal suspensions on smart surfaces by synchrotron radiation micro- and nano-beams

KAUST Repository

Marinaro, Giovanni

2015-03-01

Droplets with colloidal biological suspensions evaporating on substrates with defined wetting properties generate confined environments for initiating aggregation and self-assembly processes. We describe smart micro- and nanostructured surfaces, optimized for probing single droplets and residues by synchrotron radiation micro- and nanobeam diffraction techniques. Applications are presented for Ac-IVD and β-amyloid (1-42) peptides capable of forming cross-β sheet structures. Complementary synchrotron radiation FTIR microspectroscopy addresses secondary structure formation. The high synchrotron radiation source brilliance enables fast raster-scan experiments. © 2015 Elsevier Ltd.

Probing droplets with biological colloidal suspensions on smart surfaces by synchrotron radiation micro- and nano-beams

KAUST Repository

Marinaro, Giovanni; Accardo, Angelo; Benseny-Cases, Nú ria; Burghammer, Manfred C.; Castillo-Michel, Hiram A.; Cotte, Marine; Dante, Silvia; De Angelis, Francesco De; Di Cola, Emanuela; Di Fabrizio, Enzo M.; Hauser, C.; Riekel, Christian

2015-01-01

Droplets with colloidal biological suspensions evaporating on substrates with defined wetting properties generate confined environments for initiating aggregation and self-assembly processes. We describe smart micro- and nanostructured surfaces, optimized for probing single droplets and residues by synchrotron radiation micro- and nanobeam diffraction techniques. Applications are presented for Ac-IVD and β-amyloid (1-42) peptides capable of forming cross-β sheet structures. Complementary synchrotron radiation FTIR microspectroscopy addresses secondary structure formation. The high synchrotron radiation source brilliance enables fast raster-scan experiments. © 2015 Elsevier Ltd.

Probing the equilibrium dynamics of colloidal hard spheres above the mode-coupling glass transition

NARCIS (Netherlands)

Brambilla, G.; al Masri, J.H.M.; Pierno, M.; Berthier, L.; Cipelletti, L.

2010-01-01

We use dynamic light scattering and computer simulations to study equilibrium dynamics and dynamic heterogeneity in concentrated suspensions of colloidal hard spheres. Our study covers an unprecedented density range and spans seven decades in structural relaxation time, , including equilibrium

Numerical and experimental analysis of the sedimentation of spherical colloidal suspensions under centrifugal force

Science.gov (United States)

Antonopoulou, Evangelia; Rohmann-Shaw, Connor F.; Sykes, Thomas C.; Cayre, Olivier J.; Hunter, Timothy N.; Jimack, Peter K.

2018-03-01

Understanding the sedimentation behaviour of colloidal suspensions is crucial in determining their stability. Since sedimentation rates are often very slow, centrifugation is used to expedite sedimentation experiments. The effect of centrifugal acceleration on sedimentation behaviour is not fully understood. Furthermore, in sedimentation models, interparticle interactions are usually omitted by using the hard-sphere assumption. This work proposes a one-dimensional model for sedimentation using an effective maximum volume fraction, with an extension for sedimentation under centrifugal force. A numerical implementation of the model using an adaptive finite difference solver is described. Experiments with silica suspensions are carried out using an analytical centrifuge. The model is shown to be a good fit with experimental data for 480 nm spherical silica, with the effects of centrifugation at 705 rpm studied. A conversion of data to Earth gravity conditions is proposed, which is shown to recover Earth gravity sedimentation rates well. This work suggests that the effective maximum volume fraction accurately captures interparticle interactions and provides insights into the effect of centrifugation on sedimentation.

Ethanol vapor-induced fabrication of colloidal crystals with controllable layers and photonic properties.

Science.gov (United States)

Zhou, Chuanqiang; Gong, Xiangxiang; Han, Jie; Guo, Rong

2015-04-07

A novel fabrication method for colloidal crystals has been proposed for the first time in this research. In this method, a suspension droplet containing colloidal particles was first spread onto a glass substrate placed in an ethanol vapor environment, and then the droplet was extracted from its center. In that case, the contact angle of the droplet reduced and the contact line receded toward the center, during which the colloidal particles self-assembled and immobilized forming a 2D colloidal crystal film on the substrate upon drying the liquid film. Alternately spreading and drying of suspension films could construct fine multi-layers of colloidal crystals, while the ethanol fraction in the suspension would be used to control roughly but rapidly the layer numbers of colloidal crystals. It was also found that the photonic properties of resultant colloidal crystal films were elevated by increasing their thickness.

Effective viscous flow properties for fiber suspensions under concentrated conditions

International Nuclear Information System (INIS)

Christensen, R.M.

1993-01-01

The effective longitudinal and transverse shear viscosities are derived for an aligned fiber suspension. The solutions are valid under very concentrated conditions for a hexagonal arrangement of the single size fibers. The results compliment the classical dilute suspension forms at the other extreme of concentration. Empirical forms are constructed to cover the full range of volume fraction of the fiber phase. Also, single size spherical particle suspensions are given a similar treatment to that of the fiber case

Influence of the initial state of carbon nanotubes on their colloidal stability under natural conditions

International Nuclear Information System (INIS)

Schwyzer, Irene; Kaegi, Ralf; Sigg, Laura; Magrez, Arnaud; Nowack, Bernd

2011-01-01

The colloidal stability of dry and suspended carbon nanotubes (CNTs) in the presence of amphiphilic compounds (i.e. natural organic matter or surfactants) at environmentally realistic concentrations was investigated over several days. The suspensions were analyzed for CNT concentration (UV-vis spectroscopy), particle size (nanoparticle tracking analysis), and CNT length and dispersion quality (TEM). When added in dry form, around 1% of the added CNTs remained suspended. Pre-dispersion in organic solvent or anionic detergent stabilized up to 65% of the added CNTs after 20 days of mild shaking and 5 days of settling. The initial state of the CNTs (dry vs. suspended) and the medium composition hence are critical determinants for the partitioning of CNTs between sediment and the water column. TEM analysis revealed that single suspended CNTs were present in all suspensions and that shaking and settling resulted in a fractionation of the CNTs with shorter CNTs remaining predominantly in suspension. - Highlights: → Individually suspended CNTs are present under environment relevant conditions. → The number of suspended CNTs varies depending on the medium composition. → Surfactants at environmental concentrations have no suspending effect on dry CNTs. → Pre-dispersed CNTs are more stable in suspension than dry CNTs. - The colloidal stability of CNTs varies a lot depending on the initial state of the CNTs (dry vs. pre-dispersed), the applied dispersant for pre-suspension, and the composition of the medium.

Rheological Properties of Aqueous Nanometric Alumina Suspensions

Energy Technology Data Exchange (ETDEWEB)

Li, Chuanping [Iowa State Univ., Ames, IA (United States)

2004-01-01

Colloidal processing is an effective and reliable approach in the fabrication of the advanced ceramic products. Successful colloidal processing of fine ceramic powders requires accurate control of the rheological properties. The accurate control relies on the understanding the influences of various colloidal parameters on the rheological properties. Almost all research done on the rheology paid less attention to the interactions of particle and solvent. However, the interactions of the particles are usually built up through the media in which the particles are suspended. Therefore, interactions of the particle with the media, the adsorbed layers on the particle surface, and chemical and physical properties of media themselves must influence the rheology of the suspension, especially for the dense suspensions containing nanosized particles. Relatively little research work has been reported in this area. This thesis addresses the rheological properties of nanometric alumina aqueous suspensions, and paying more attention to the interactions between particle and solvent, which in turn influence the particle-particle interactions. Dense nanometric alumina aqueous suspensions with low viscosity were achieved by environmentally-benign fructose additives. The rheology of nanometric alumina aqueous suspensions and its variation with the particle volume fraction and concentration of fructose were explored by rheometry. The adsorptions of solute (fructose) and solvent (water) on the nanometric alumina particle surfaces were measured and analyzed by TG/DSC, TOC, and NMR techniques. The mobility of water molecules in the suspensions and its variation with particle volume fractions and fructose additive were determined by the ¹⁷O NMR relaxation method. The interactions between the nanometric alumina particles in water and fructose solutions were investigated by AFM. The results indicated that a large number of water layers were physically bound on the particles

Effect of sonication on the colloidal stability of iron oxide nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Sodipo, Bashiru Kayode [Nano-Optoelectronics Research and Technology (NOR) Lab, School of Physics, Universiti Sains Malaysia, 11800 Pulau Pinang (Malaysia); Aziz, Azlan Abdul [Nano-Biotechnology Research and Innovation (NanoBRI), Institute for Research in Molecular Medicine (INFORMM), Universiti Sains Malaysia, 11800, Pulau Pinang (Malaysia)

2015-04-24

Colloidal stability of superparamagnetic iron oxide nanoparticles’ (SPION) suspensions, ultrasonically irradiated at various pH was studied. Electrophoresis measurement of the sonicated SPION showed that the shock waves and other unique conditions generated from the acoustic cavitation process (formation, growth and collapse of bubbles) affect the zeta potential value of the suspension. In this work, stabled colloidal suspensions of SPION were prepared and their pH is varied between 3 and 5. Prior to ultrasonic irradiation of the suspensions, their initial zeta potential values were determined. After ultrasonic irradiation of the suspensions, we observed that the sonication process interacts with colloidal stability of the nanoparticles. The results demonstrated that only suspensions with pH less 4 were found stable and able to retain more than 90% of its initial zeta potential value. However, at pH greater than 4, the suspensions were found unstable. The result implies that good zeta potential value of SPION can be sustained in sonochemical process as long as the pH of the mixture is kept below 4.

Transport coefficients and mechanical response in hard-disk colloidal suspensions

Science.gov (United States)

Zhang, Bo-Kai; Li, Jian; Chen, Kang; Tian, Wen-De; Ma, Yu-Qiang

2016-11-01

We investigate the transport properties and mechanical response of glassy hard disks using nonlinear Langevin equation theory. We derive expressions for the elastic shear modulus and viscosity in two dimensions on the basis of thermal-activated barrier-hopping dynamics and mechanically accelerated motion. Dense hard disks exhibit phenomena such as softening elasticity, shear-thinning of viscosity, and yielding upon deformation, which are qualitatively similar to dense hard-sphere colloidal suspensions in three dimensions. These phenomena can be ascribed to stress-induced “landscape tilting”. Quantitative comparisons of these phenomena between hard disks and hard spheres are presented. Interestingly, we find that the density dependence of yield stress in hard disks is much more significant than in hard spheres. Our work provides a foundation for further generalizing the nonlinear Langevin equation theory to address slow dynamics and rheological behavior in binary or polydisperse mixtures of hard or soft disks. Project supported by the National Basic Research Program of China (Grant No. 2012CB821500) and the National Natural Science Foundation of China (Grant Nos. 21374073 and, 21574096).

Increasing surface enhanced Raman spectroscopy effect of RNA and DNA components by changing the pH of silver colloidal suspensions.

Science.gov (United States)

Primera-Pedrozo, Oliva M; Rodríguez, Gabriela Del Mar; Castellanos, Jorge; Felix-Rivera, Hilsamar; Resto, Oscar; Hernández-Rivera, Samuel P

2012-02-15

This work focused on establishing the parameters for enhancing the Raman signals of DNA and RNA constituents: nitrogenous bases, nucleosides and nucleotides, using metallic nanoparticles as surface enhanced Raman scattering substrates. Silver nanospheres were synthesized using sodium borohydride as a reducing agent and sodium citrate as a capping agent. The prepared nanoparticles had a surface plasmon band at ∼384nm and an average size of 12±3nm. The nanoparticles' surface charge was manipulated by changing the pH of the Ag colloidal suspensions in the range of 1-13. Low concentrations as 0.7μM were detected under the experimental conditions. The optimum pH values were: 7 for adenine, 9 for AMP, 5 for adenosine, 7 for dAMP and 11 for deoxyadenosine. Copyright © 2011 Elsevier B.V. All rights reserved.

Colloid Mobilization in Two Atlantic Coastal Plain Aquifers: Field Studies

Science.gov (United States)

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.

Non-equilibrium relaxation and near-arrest dynamics in colloidal suspensions

International Nuclear Information System (INIS)

Medina-Noyola, M; RamIrez-Gonzalez, Pedro

2009-01-01

In this work we propose a theory to describe the irreversible diffusive relaxation of the local concentration of a colloidal dispersion that proceeds toward its stable thermodynamic equilibrium state, but which may in the process be trapped in metastable or dynamically arrested states. The central assumption of this theory is that the irreversible relaxation of the macroscopically observed mean value n-bar(r,t) of the local concentration of colloidal particles is described by a diffusion equation involving a local mobility b*(r,t) that depends not only on the mean value n-bar(r,t) but also on the covariance σ(r,r';t)≡δn(r,t)δn(r',t)-bar of the fluctuations δn(r,t)≡n(r,t)-n-bar(r,t). This diffusion equation must hence be solved simultaneously with the relaxation equation for the covariance σ(r,r';t), and here we also derive the corresponding relaxation equation. The dependence of the local mobility b*(r,t) on the mean value and the covariance is determined by a self-consistent set of equations involving now the spatially and temporally non-local time-dependent correlation functions, which in a uniform system in equilibrium reduces to the self-consistent generalized Langevin equation (SCGLE) theory of colloid dynamics. The resulting general theory considers the possibility that these relaxation processes occur under the influence of external fields, such as gravitational forces acting in the process of sedimentation. In this paper, however, we describe a simpler application, in which the system remains spatially uniform during the irreversible relaxation process, and discuss the general features of the glass transition scenario predicted by this non-equilibrium theory.

Stilbazolium Merocyanine Dye Determination in Different Solutions, Concentrations and Colloids Using SERS

DEFF Research Database (Denmark)

Pajchrowski, Grzegorz; Abdali, Salim; Nørbygaard, Thomas

2006-01-01

Surface Enhanced Raman Scattering (SERS) measurements were carried out on stilbazolium merocyanine dye in methanol and pyridine solvents. Both solutions were measured in series of concentrations, covering a range of 5·10-5 M to 5·10-8 M. In these measurements Ag and Au colloids were used and the ......Surface Enhanced Raman Scattering (SERS) measurements were carried out on stilbazolium merocyanine dye in methanol and pyridine solvents. Both solutions were measured in series of concentrations, covering a range of 5·10-5 M to 5·10-8 M. In these measurements Ag and Au colloids were used...... report here on the success of using SERS to obtain Raman spectra of merocyanine dye at very low concentration in an attempt of new approach, which can be used for further investigations of the dye. The SERS spectra will here be reported and the results from different solutions, colloids, concentrations...

Some aspects related to stability, critical concentrations and kinetics of flocculation of the calcium phytate colloid

International Nuclear Information System (INIS)

Lucas, F.J.M.; Alvarez, J.G.; Sanchis, S.E.; Munoz, B.C.

1986-01-01

As sup(99m)Tc-Ca phytate is an important radiopharmaceutical and its colloidal nature presents problems, we investigated some of them. This work describes the study of the colloidal behaviour of the calcium phytate colloid in terms of its formation, stability and kinetics of flocculation. The study of spontaneous, and centrifugation-induced flocculation allows the determination of two critical concentrations of sol flocculation. The titrations of calcium phytate colloid at different concentrations provide information on the colloidal formation conditions. Moreover, a study on flocculation kinetics was made by turbidity measurements. (author)

An Experimental Study of the Equation of State of Nano Colloids Using a Novel Dielectrophoresis Osmometer

Science.gov (United States)

Shen, Chong; Sirorattanakul, Krittanon; Huang, Hao; Ou-Yang, H. Daniel

This talk reports a novel method to measure equation of state (EOS) relating the colloidal osmotic pressure with particle concentration. Recent theories and simulations have made predictions for such EOS for various particle interactions, but measurements are rare. Conventional methods to determine the osmotic pressure in colloid suspensions use gravity or centrifugation. However, the nano colloidal system requires a long time to reach equilibrium when the particle sizes are small or their mass densities are close to that of the solvent. Here, we propose a new method involving electric bottle that will solve all such challenges. In the equilibrium under dielectrophoresis (DEP) force field, the spatial distribution of the particle density can be determined from fluorescent microscopy. According to Einstein's osmotic equilibrium theory, the osmotic pressure of the colloid suspensions can be calculated. Then, the DEP force field is calibrated using the well-established EOS of colloidal hard spheres. Using the known force field, we determine the EOS for other particles with various interactions and compare the results with theoretical predictions. This work supports by NSF-DMR 0923299, Lehigh department of physics, Emulsion Polymers Institute.

Automated preparation method for colloidal crystal arrays of monodisperse and binary colloid mixtures by contact printing with a pintool plotter.

Science.gov (United States)

Burkert, Klaus; Neumann, Thomas; Wang, Jianjun; Jonas, Ulrich; Knoll, Wolfgang; Ottleben, Holger

2007-03-13

Photonic crystals and photonic band gap materials with periodic variation of the dielectric constant in the submicrometer range exhibit unique optical properties such as opalescence, optical stop bands, and photonic band gaps. As such, they represent attractive materials for the active elements in sensor arrays. Colloidal crystals, which are 3D gratings leading to Bragg diffraction, are one potential precursor of such optical materials. They have gained particular interest in many technological areas as a result of their specific properties and ease of fabrication. Although basic techniques for the preparation of regular patterns of colloidal crystals on structured substrates by self-assembly of mesoscopic particles are known, the efficient fabrication of colloidal crystal arrays by simple contact printing has not yet been reported. In this article, we present a spotting technique used to produce a microarray comprising up to 9600 single addressable sensor fields of colloidal crystal structures with dimensions down to 100 mum on a microfabricated substrate in different formats. Both monodisperse colloidal crystals and binary colloidal crystal systems were prepared by contact printing of polystyrene particles in aqueous suspension. The array morphology was characterized by optical light microscopy and scanning electron microscopy, which revealed regularly ordered crystalline structures for both systems. In the case of binary crystals, the influence of the concentration ratio of the large and small particles in the printing suspension on the obtained crystal structure was investigated. The optical properties of the colloidal crystal arrays were characterized by reflection spectroscopy. To examine the stop bands of the colloidal crystal arrays in a high-throughput fashion, an optical setup based on a CCD camera was realized that allowed the simultaneous readout of all of the reflection spectra of several thousand sensor fields per array in parallel. In agreement with

Radiometric method for the characterization of particulate processes in colloidal suspensions. II. Experimental verification of the method

Energy Technology Data Exchange (ETDEWEB)

Subotic, B. [Institut Rudjer Boskovic, Zagreb (Yugoslavia)

1979-09-15

A radiometric method for the characterization of particulate processes is verified using stable hydrosols of silver iodide. Silver iodide hydrosols satisfy the conditions required for the applications of the proposed method. Comparison shows that the values for the change of particle size measured in silver iodide hydrosols by the proposed method are in excellent agreement with the values obtained by other methods on the same systems (electron microscopy, sedimentation analysis, light scattering). This shows that the proposed method is suitable for the characterization of particulate processes in colloidal suspensions. (Auth.).

Dynamic assembly of ultrasoft colloidal networks enables cell invasion within restrictive fibrillar polymers

Science.gov (United States)

Douglas, Alison M.; Fragkopoulos, Alexandros A.; Gaines, Michelle K.; Lyon, L. Andrew; Fernandez-Nieves, Alberto; Barker, Thomas H.

2017-01-01

In regenerative medicine, natural protein-based polymers offer enhanced endogenous bioactivity and potential for seamless integration with tissue, yet form weak hydrogels that lack the physical robustness required for surgical manipulation, making them difficult to apply in practice. The use of higher concentrations of protein, exogenous cross-linkers, and blending synthetic polymers has all been applied to form more mechanically robust networks. Each relies on generating a smaller network mesh size, which increases the elastic modulus and robustness, but critically inhibits cell spreading and migration, hampering tissue regeneration. Here we report two unique observations; first, that colloidal suspensions, at sufficiently high volume fraction (ϕ), dynamically assemble into a fully percolated 3D network within high-concentration protein polymers. Second, cells appear capable of leveraging these unique domains for highly efficient cell migration throughout the composite construct. In contrast to porogens, the particles in our system remain embedded within the bulk polymer, creating a network of particle-filled tunnels. Whereas this would normally physically restrict cell motility, when the particulate network is created using ultralow cross-linked microgels, the colloidal suspension displays viscous behavior on the same timescale as cell spreading and migration and thus enables efficient cell infiltration of the construct through the colloidal-filled tunnels.

Colloidal behavior of aqueous montmorillonite suspensions in the presence of non-ionic polymer

Science.gov (United States)

Gareche, M.; Azri, N.; Allal, A.; Zeraibi, N.

2015-04-01

In this paper we characterized at first, the rheological behavior of the bentonite suspensions and the aqueous solutions of polyethylene oxide (PEO), then we were investigated the influence of this polymer in a water-based drilling fluid model (6% of bentonite suspension). The objective is to exhibit how the non ionic polymer with molecular weight 6×103 g/mol. of varying concentration mass (0.7%, 1%, 2% et 3%) significantly alter the rheological properties (yield stress, viscosity, loss and elastic modulus) of the bentonite suspensions. The rheological measurements made in simple shear and in dynamic on the mixture (water-bentonite-PEO), showed rheological properties of bentonite suspensions both in the presence and absence of non-ionic polymer. The PEO presents an affinity for the bentonite particles slowing down their kinetic aggregation. The analysis by X-rays diffraction also allowed understanding the structure of this mixture. It had revealed the intercalation between of the clay platelets on one hand, and the links bridges assured by the chains of polymer between bentonite particles beyond a critical concentration in PEO on the other hand. The Herschel- Bulkley rheological model is used for the correlation of our experimental results.

Colloidal behavior of aqueous montmorillonite suspensions in the presence of non-ionic polymer

International Nuclear Information System (INIS)

Gareche, M; Azri, N; Zeraibi, N; Allal, A

2015-01-01

In this paper we characterized at first, the rheological behavior of the bentonite suspensions and the aqueous solutions of polyethylene oxide (PEO), then we were investigated the influence of this polymer in a water-based drilling fluid model (6% of bentonite suspension). The objective is to exhibit how the non ionic polymer with molecular weight 6×10 3 g/mol. of varying concentration mass (0.7%, 1%, 2% et 3%) significantly alter the rheological properties (yield stress, viscosity, loss and elastic modulus) of the bentonite suspensions. The rheological measurements made in simple shear and in dynamic on the mixture (water-bentonite-PEO), showed rheological properties of bentonite suspensions both in the presence and absence of non-ionic polymer. The PEO presents an affinity for the bentonite particles slowing down their kinetic aggregation. The analysis by X-rays diffraction also allowed understanding the structure of this mixture. It had revealed the intercalation between of the clay platelets on one hand, and the links bridges assured by the chains of polymer between bentonite particles beyond a critical concentration in PEO on the other hand. The Herschel- Bulkley rheological model is used for the correlation of our experimental results. (paper)

Transport and Deposition of Variably Charged Soil Colloids in Saturated Porous Media

DEFF Research Database (Denmark)

Sharma, Anu; Kawamoto, Ken; Møldrup, Per

2011-01-01

Okinawa (RYS colloids) in Japan. The VAS colloids exhibited a negative surface charge with a high pH dependency, whereas the RYS colloids exhibited a negative surface charge with less pH dependency. The soil colloids were applied as colloidal suspensions to 10-cm-long saturated sand columns packed...

Manipulating colloids with charges and electric fields

NARCIS (Netherlands)

Leunissen, M.E.

2007-01-01

This thesis presents the results of experimental investigations on a variety of colloidal suspensions. Colloidal particles are at least a hundred times larger than atoms or molecules, but suspended in a liquid they display the same phase behavior, including fluid and crystalline phases. Due to their

Simulating colloid hydrodynamics with lattice Boltzmann methods

International Nuclear Information System (INIS)

Cates, M E; Stratford, K; Adhikari, R; Stansell, P; Desplat, J-C; Pagonabarraga, I; Wagner, A J

2004-01-01

We present a progress report on our work on lattice Boltzmann methods for colloidal suspensions. We focus on the treatment of colloidal particles in binary solvents and on the inclusion of thermal noise. For a benchmark problem of colloids sedimenting and becoming trapped by capillary forces at a horizontal interface between two fluids, we discuss the criteria for parameter selection, and address the inevitable compromise between computational resources and simulation accuracy

Colloidal processing and rapid prototyping of Si{sub 3}N{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Liwu Wang

1998-12-01

Some progresses have been made in the wet shaping of Si{sub 3}N{sub 4} based on a better understanding of the colloidal behavior of suspensions and by improved pressure casting with porous polystyrene (PS) molds. This work illustrated that the combination of proper colloidal processing and rapid prototyping is an effective way to fabricate high-performance ceramics with complex shapes. In colloidal processing the packing density and microstructure of green bodies can be controlled if the interaction between ceramic particles in suspensions and the conditions under which the suspensions are consolidated are understood. Therefore, detailed studies on the surface chemistry of the Si{sub 3}N{sub 4} powder, the dispersing behavior of Si{sub 3}N{sub 4} suspensions, the influence of dispersants and the mechanism during powder consolidation into complex-shaped green bodies are performed. (orig.)

Rheology of dense suspensions of non colloidal particles

Science.gov (United States)

Guazzelli, Élisabeth

2017-06-01

Dense suspensions are materials with broad applications both in industrial processes (e.g. waste disposal, concrete, drilling muds, metalworking chip transport, and food processing) and in natural phenomena (e.g. flows of slurries, debris, and lava). Despite its long research history and its practical relevance, the mechanics of dense suspensions remain poorly understood. The major difficulty is that the grains interact both by hydrodynamic interactions through the liquid and by mechanical contact. These systems thus belong to an intermediate regime between pure suspensions and granular flows. We show that we can unify suspension and granular rheology under a common framework by transferring the frictional approach of dry granular media to wet suspensions of spherical particles. We also discuss non-Newtonian behavior such as normal-stress differences and shear-induced migration. Beyond the classical problem of dense suspension of hard spheres which is far from being completely resolved, there are also entirely novel avenues of study concerning more complex mixtures of particles and fluids such as those involving other types of particles (e.g. fibers) or non-Newtonian fluids that we will also address.

Concentrations and compositions of colloidal particles in groundwater near the ICPP, Idaho National Laboratory, Idaho

International Nuclear Information System (INIS)

Estes, M.; McCurry, M.

1994-01-01

The presence of colloidal material is being investigated in groundwater near the ICPP to determine whether the concentrations and chemical compositions are suitable to have an impact on the transport of Sr-90. Colloids are proposed as a viable transport mechanism, and may have an influence on the chemical trends observed in three wells near the ICPP. Ultrafiltration of groundwater samples has been performed on difFerent intervals in USGS wells 45, 46, and Site 14, has provided filtrate samples, for analyses by ICP-MS, and filters for analyses by SEM/EDS. Preliminary results indicate that concentrations of colloids are from 2.1-0.8 ppm for the >0.45 μm size fraction, and 2.3-9.8 ppm for the <0.45 μm size fractions. Compositions consist of calcite, silicic acid, ferrihydrite, clay, and possibly dolomite. Calcium was shown to have the largest contribution from both EDS and ICP-MS. Magnesium and silicon were also found to filter out in large concentrations. Iron and aluminum are minor constituents of the colloidal mass and contain concentrations of <10ppb and <1ppb, respectively. These results indicate that if colloids are going to have a major impact on contaminant migration then the coprecipitation of Sr-90 with calcite and dolomite would have to be a sorption mechanism. Sorption onto Fe and Al colloids probably does not have a major impact because of the low concentrations. Clay colloids were noted to be relatively abundant and may also have an impact on Sr-90 migration, due to the exchange of Sr with other cations in the clay structure. 14 refs., 4 figs., 2 tabs

Suspension Hydrogen Reduction of Iron Oxide Concentrates

Energy Technology Data Exchange (ETDEWEB)

H.Y. Sohn

2008-03-31

The objective of the project is to develop a new ironmaking technology based on hydrogen and fine iron oxide concentrates in a suspension reduction process. The ultimate objective of the new technology is to replace the blast furnace and to drastically reduce CO2 emissions in the steel industry. The goals of this phase of development are; the performance of detailed material and energy balances, thermochemical and equilibrium calculations for sulfur and phosphorus impurities, the determination of the complete kinetics of hydrogen reduction and bench-scale testing of the suspension reduction process using a large laboratory flash reactor.

Rheology of dense suspensions of non colloidal particles

Directory of Open Access Journals (Sweden)

Guazzelli Élisabeth

2017-01-01

Full Text Available Dense suspensions are materials with broad applications both in industrial processes (e.g. waste disposal, concrete, drilling muds, metalworking chip transport, and food processing and in natural phenomena (e.g. flows of slurries, debris, and lava. Despite its long research history and its practical relevance, the mechanics of dense suspensions remain poorly understood. The major difficulty is that the grains interact both by hydrodynamic interactions through the liquid and by mechanical contact. These systems thus belong to an intermediate regime between pure suspensions and granular flows. We show that we can unify suspension and granular rheology under a common framework by transferring the frictional approach of dry granular media to wet suspensions of spherical particles. We also discuss non-Newtonian behavior such as normal-stress differences and shear-induced migration. Beyond the classical problem of dense suspension of hard spheres which is far from being completely resolved, there are also entirely novel avenues of study concerning more complex mixtures of particles and fluids such as those involving other types of particles (e.g. fibers or non-Newtonian fluids that we will also address.

Crack formation and prevention in colloidal drops

Science.gov (United States)

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

2015-08-01

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

Bio-inactivation of human malignant cells through highly responsive diluted colloidal suspension of functionalized magnetic iron oxide nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Ferreira, Roberta V. [Federal Center of Technological Education of Minas Gerais, Department of Materials (Brazil); Silva-Caldeira, Priscila P. [Federal Center of Technological Education of Minas Gerais, Department of Chemistry (Brazil); Pereira-Maia, Elene C.; Fabris, José D.; Cavalcante, Luis Carlos D. [Federal University of Minas Gerais (UFMG), Department of Chemistry – ICEx (Brazil); Ardisson, José D. [Nuclear Technology Development Center (CDTN) (Brazil); Domingues, Rosana Z., E-mail: rosanazd@yahoo.com.br, E-mail: rosanazd@ufmg.br [Federal University of Minas Gerais (UFMG), Department of Chemistry – ICEx (Brazil)

2016-04-15

Magnetic fluids, more specifically aqueous colloidal suspensions containing certain magnetic nanoparticles (MNPs), have recently been gaining special interest due to their potential use in clinical treatments of cancerous formations in mammalians. The technological application arises mainly from their hyperthermic behavior, which means that the nanoparticles dissipate heat upon being exposed to an alternating magnetic field (AMF). If the temperature is raised to slightly above 43 °C, cancer cells are functionally inactivated or killed; however, normal cells tend to survive under those same conditions, entirely maintaining their bioactivity. Recent in vitro studies have revealed that under simultaneous exposure to an AMF and magnetic nanoparticles, certain lines of cancer cells are bio-inactivated even without experiencing a significant temperature increase. This non-thermal effect is cell specific, indicating that MNPs, under alternating magnetic fields, may effectively kill cancer cells under conditions that were previously thought to be implausible, considering that the temperature does not increase more than 5 °C, which is also true in cases for which the concentration of MNPs is too low. To experimentally test for this effect, this study focused on the feasibility of inducing K562 cell death using an AMF and aqueous suspensions containing very low concentrations of MNPs. The assay was designed for a ferrofluid containing magnetite nanoparticles, which were obtained through the co-precipitation method and were functionalized with citric acid; the particles had an average diameter of 10 ± 2 nm and a mean hydrodynamic diameter of approximately 40 nm. Experiments were first performed to test for the ability of the ferrofluid to release heat under an AMF. The results show that for concentrations ranging from 2.5 to 1.0 × 10{sup 3} mg L{sup −1}, the maximum temperature increase was actually less than 2 °C. However, the in vitro test results from K

Parameters for Fabricating Nano-Au Colloids through the Electric Spark Discharge Method with Micro-Electrical Discharge Machining.

Science.gov (United States)

Tseng, Kuo-Hsiung; Chung, Meng-Yun; Chang, Chaur-Yang

2017-06-02

In this study, the Electric Spark Discharge Method (ESDM) was employed with micro-electrical discharge machining (m-EDM) to create an electric arc that melted two electrodes in deionized water (DW) and fabricated nano-Au colloids through pulse discharges with a controlled on-off duration (T ON -T OFF ) and a total fabrication time of 1 min. A total of six on-off settings were tested under normal experimental conditions and without the addition of any chemical substances. Ultraviolet-visible spectroscopy (UV-Vis), Zetasizer Nano measurements, and scanning electron microscopy-energy dispersive X-ray (SEM-EDX) analyses suggested that the nano-Au colloid fabricated at 10-10 µs (10 µs on, 10 µs off) had higher concentration and suspension stability than products made at other T ON -T OFF settings. The surface plasmon resonance (SPR) of the colloid was 549 nm on the first day of fabrication and stabilized at 532 nm on the third day. As the T ON -T OFF period increased, the absorbance (i.e., concentration) of all nano-Au colloids decreased. Absorbance was highest at 10-10 µs. The SPR peaks stabilized at 532 nm across all T ON -T OFF periods. The Zeta potential at 10-10 µs was -36.6 mV, indicating that no nano-Au agglomeration occurred and that the particles had high suspension stability.

Determining Quiescent Colloidal Suspension Viscosities Using the Green-Kubo Relation and Image-Based Stress Measurements

Science.gov (United States)

Lin, Neil Y. C.; Bierbaum, Matthew; Cohen, Itai

2017-09-01

By combining confocal microscopy and stress assessment from local structural anisotropy, we directly measure stresses in 3D quiescent colloidal liquids. Our noninvasive and nonperturbative method allows us to measure forces ≲50 fN with a small and tunable probing volume, enabling us to resolve the stress fluctuations arising from particle thermal motions. We use the Green-Kubo relation to relate these measured stress fluctuations to the bulk Brownian viscosity at different volume fractions, comparing against simulations and conventional rheometry measurements. We find that the Green-Kubo analysis gives excellent agreement with these prior results, suggesting that similar methods could be applied to investigations of local flow properties in many poorly understood far-from-equilibrium systems, including suspensions that are glassy, strongly sheared, or highly confined.

Size determinations of plutonium colloids using autocorrelation photon spectroscopy

International Nuclear Information System (INIS)

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

1989-01-01

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

Large Scale Brownian Dynamics of Confined Suspensions of Rigid Particles

Science.gov (United States)

Donev, Aleksandar; Sprinkle, Brennan; Balboa, Florencio; Patankar, Neelesh

2017-11-01

We introduce new numerical methods for simulating the dynamics of passive and active Brownian colloidal suspensions of particles of arbitrary shape sedimented near a bottom wall. The methods also apply for periodic (bulk) suspensions. Our methods scale linearly in the number of particles, and enable previously unprecedented simulations of tens to hundreds of thousands of particles. We demonstrate the accuracy and efficiency of our methods on a suspension of boomerang-shaped colloids. We also model recent experiments on active dynamics of uniform suspensions of spherical microrollers. This work was supported in part by the National Science Foundation under award DMS-1418706, and by the U.S. Department of Energy under award DE-SC0008271.

Effect of concentration on the rheology and serum separation of tomato suspensions

NARCIS (Netherlands)

Ouden, den F.W.C.; Vliet, van T.

2002-01-01

The °Brix value of the tomato concentrate, from which tomato suspensions were prepared, was shown to have a large effect on the resulting apparent viscosity and storage modulus. The apparent viscosity of a tomato suspension prepared from a 30 °Brix tomato concentrate was only 35␘f that of a

Origins of microstructural transformations in charged vesicle suspensions: the crowding hypothesis.

Science.gov (United States)

Seth, Mansi; Ramachandran, Arun; Murch, Bruce P; Leal, L Gary

2014-09-02

It is observed that charged unilamellar vesicles in a suspension can spontaneously deflate and subsequently transition to form bilamellar vesicles, even in the absence of externally applied triggers such as salt or temperature gradients. We provide strong evidence that the driving force for this deflation-induced transition is the repulsive electrostatic pressure between charged vesicles in concentrated suspensions, above a critical effective volume fraction. We use volume fraction measurements and cryogenic transmission electron microscopy imaging to quantitatively follow both the macroscopic and microstructural time-evolution of cationic diC18:1 DEEDMAC vesicle suspensions at different surfactant and salt concentrations. A simple model is developed to estimate the extent of deflation of unilamellar vesicles caused by electrostatic interactions with neighboring vesicles. It is determined that when the effective volume fraction of the suspension exceeds a critical value, charged vesicles in a suspension can experience "crowding" due to overlap of their electrical double layers, which can result in deflation and subsequent microstructural transformations to reduce the effective volume fraction of the suspension. Ordinarily in polydisperse colloidal suspensions, particles interacting via a repulsive potential transform into a glassy state above a critical volume fraction. The behavior of charged vesicle suspensions reported in this paper thus represents a new mechanism for the relaxation of repulsive interactions in crowded situations.

A study of the effect of certain formulation variables on the mucoadhesive properties of per oral sucralfate suspensions

Science.gov (United States)

Dobrozsi, Douglas Joseph

1999-10-01

The primary objective of this research was to evaluate the effect of formulation variables on the ability of a suspension of the material sucralfate to be triggered to gel by components of the gastrointestinal fluid and in so doing, act as an in situ gelling mucoadhesive liquid. The particle size and type of sucralfate raw material, suspension pH, ionic strength, and presence of the humectant suspension aid glycerin were studied. Sucralfate materials were prepared in sizes ranging from under 50 nanometers up to 60 microns. Included were conventional powders, and a gel form prepared by controlled precipitation from acid solution. Sucralfate zero point of charge was determined by titration to be pH 4.8--4.9 for powder, and 5--5.3 for gel. The gel was found to exist as aggregates of a relatively uniform, spherical, nanoparticulate colloidal sol with particle size in the range of 50 to 400 nanometers. The aggregates could be disrupted by high pressure homogenization so that individual colloidal particles could be detected in water dispersion. Rheologic and mucoadhesion evaluations of suspensions were conducted. Models were established for in vitro mucoadhesion by rheologic synergism with mucin, and for mucosal coating and retention on rat esophagus ex vivo. Experiments with marketed sucralfate suspensions indicated that rheologic synergism with gastric mucin correlated with ex vivo mucoretention and agreed directionally with published human mucoretention. Aqueous suspension viscosity was found to be increased by KCl, by increasing sucralfate concentration, and for the gel by adjusting pH near the zero point of charge. Viscosity also increased with decreasing sucralfate particle size but rheologic synergism did not correlate with particle size. Glycerin increased rheologic synergism with mucin. Suspension viscosity and rheologic synergism were much greater under all conditions for sucralfate gel suspensions than for sucralfate powder suspensions. Disruption of gel

Origins of the anomalous stress behavior in charged colloidal suspensions under shear.

Science.gov (United States)

Kumar, Amit; Higdon, Jonathan J L

2010-11-01

Numerical simulations are conducted to determine microstructure and rheology of sheared suspensions of charged colloidal particles at a volume fraction of ϕ=0.33. Over broad ranges of repulsive force strength F0 and Péclet number Pe, dynamic simulations show coexistence of ordered and disordered stable states with the state dependent on the initial condition. In contrast to the common view, at low shear rates, the disordered phase exhibits a lower viscosity (μ(r)) than the ordered phase, while this behavior is reversed at higher shear rates. Analysis shows the stress reversal is associated with different shear induced microstructural distortions in the ordered and disordered systems. Viscosity vs shear rate data over a wide range of F0 and Pe collapses well upon rescaling with the long-time self-diffusivity. Shear thinning viscosity in the ordered phase scaled as μ(r)∼Pe(-0.81) at low shear rates. The microstructural dynamics revealed in these studies explains the anomalous behavior and hysteresis loops in stress data reported in the literature.

Large-scale photochemical reactions of nanocrystalline suspensions: a promising green chemistry method.

Science.gov (United States)

Veerman, Marcel; Resendiz, Marino J E; Garcia-Garibay, Miguel A

2006-06-08

Photochemical reactions in the solid state can be scaled up from a few milligrams to 10 grams by using colloidal suspensions of a photoactive molecular crystal prepared by the solvent shift method. Pure products are recovered by filtration, and the use of H(2)O as a suspension medium makes this method a very attractive one from a green chemistry perspective. Using the photodecarbonylation of dicumyl ketone (DCK) as a test system, we show that reaction efficiencies in colloidal suspensions rival those observed in solution. [reaction: see text

Renormalized charge in a two-dimensional model of colloidal suspension from hypernetted chain approach.

Science.gov (United States)

Camargo, Manuel; Téllez, Gabriel

2008-04-07

The renormalized charge of a simple two-dimensional model of colloidal suspension was determined by solving the hypernetted chain approximation and Ornstein-Zernike equations. At the infinite dilution limit, the asymptotic behavior of the correlation functions is used to define the effective interactions between the components of the system and these effective interactions were compared to those derived from the Poisson-Boltzmann theory. The results we obtained show that, in contrast to the mean-field theory, the renormalized charge does not saturate, but exhibits a maximum value and then decays monotonically as the bare charge increases. The results also suggest that beyond the counterion layer near to the macroion surface, the ionic cloud is not a diffuse layer which can be handled by means of the linearized theory, as the two-state model claims, but a more complex structure is settled by the correlations between microions.

Particle Trapping and Banding in Rapid Colloidal Solidification

KAUST Repository

Elliott, J. A. W.

2011-10-11

We derive an expression for the nonequilibrium segregation coefficient of colloidal particles near a moving solid-liquid interface. The resulting kinetic phase diagram has applications for the rapid solidification of clay soils, gels, and related colloidal systems. We use it to explain the formation of bandlike defects in rapidly solidified alumina suspensions. © 2011 American Physical Society.

Unveiling the relationships among the viscosity equations of glass liquids and colloidal suspensions for obtaining universal equations with the generic free volume concept.

Science.gov (United States)

Hao, Tian

2015-09-14

The underlying relationships among viscosity equations of glass liquids and colloidal suspensions are explored with the aid of free volume concept. Viscosity equations of glass liquids available in literature are focused and found to have a same physical basis but different mathematical expressions for the free volume. The glass transitions induced by temperatures in glass liquids and the percolation transition induced by particle volume fractions in colloidal suspensions essentially are a second order phase transition: both those two transitions could induce the free volume changes, which in turn determines how the viscosities are going to change with temperatures and/or particle volume fractions. Unified correlations of the free volume to both temperatures and particle volume fractions are thus proposed. The resulted viscosity equations are reducible to many popular viscosity equations currently widely used in literature; those equations should be able to cover many different types of materials over a wide temperature range. For demonstration purpose, one of the simplified versions of those newly developed equations is compared with popular viscosity equations and the experimental data: it can well fit the experimental data over a wide temperature range. The current work reveals common physical grounds among various viscosity equations, deepening our understanding on viscosity and unifying the free volume theory across many different systems.

Colloidal agglomerates in tank sludge and their impact on waste processing

International Nuclear Information System (INIS)

Tingey, J.M.; Bunker, B.C.; Graff, G.L.; Keefer, K.D.; Lea, A.S.; Rector, D.R.

1999-01-01

Disposal of millions of gallons of existing radioactive wastes in underground storage tanks is a major remediation activity for the US Department of Energy. These wastes include a substantial volume of insoluble sludges consisting of submicron colloidal particles. Processing these sludges under the proposed processing conditions presents unique challenges in retrieval transport, separation, and solidification of these waste streams. Depending on processing conditions, these colloidal particles can form agglomerated networks having high viscosities that could clog transfer lines or produce high volumes of low-density sediments that interfere with solid-liquid separations. Under different conditions, these particles can be dispersed to form very fine suspended particles that do not settle. Given the wide range of waste chemistries present at Department of Energy sites, it is impractical to measure the properties of all treatment procedures. Under the current research activities, the underlying principles of colloid chemistry and physics are being studied to predict and eventually control the physical properties of sludge suspensions and sediment layers in tank wastes and other waste processing streams. Proposed tank processing strategies include retrieval transport, and solid-liquid separations in basic (pH 10 to 14), high ionic strength (0.1 to 1.0 M) salt solutions. The effect of salt concentration, ionic strength, and salt composition on the physical properties such as viscosity, agglomerate size, and sedimentation of model suspensions containing mixtures of one or two of the major components found in actual wastes have been measured to understand how agglomeration influences processing. Property models developed from theory and experiment on these simple suspensions are then applied to explain the results obtained on actual wastes

Spinodal decomposition in a food colloid-biopolymer mixture: evidence for a linear regime

Energy Technology Data Exchange (ETDEWEB)

Bhat, Suresh [Department of Physics and Fribourg Center for Nanomaterials, University of Fribourg, 1700 Fribourg (Switzerland); Tuinier, Remco [Forschungszentrum Juelich, Institut fuer Festkoerperforschung, 52425 Juelich (Germany); Schurtenberger, Peter [Department of Physics and Fribourg Center for Nanomaterials, University of Fribourg, 1700 Fribourg (Switzerland)

2006-07-05

We investigate phase separation and structural evolution in a complex food colloid (casein micelles) and biopolymer (xanthan) mixture using small-angle light scattering. We demonstrate that phase separation is induced by a depletion mechanism, and that the resulting coexistence curve can be described by osmotic equilibrium theory for mixtures of colloids and polymer chains in a background solvent, taking into account interactions between the polymer chains in the excluded volume limit. We show that the light scattering pattern of an unstable mixture exhibits the typical behaviour of spinodal decomposition, and we are able to confirm the validity of dynamic similarity scaling. We find three distinct regimes (initial or linear, intermediate and transition stage) for the decomposition kinetics that differ in the time dependence of the peak position of the structure factor. In particular we find clear evidence for the existence of an initial linear regime, where the peak position remains constant and the amplitude grows. The existence of spinodal-like decomposition and the validity of universal scaling in the intermediate and transition stages have been found in previous studies of phase separation in attractive colloidal suspensions. However, to our knowledge the initial linear regime has never been observed in colloidal suspensions, and we attribute this at least partly to the effect of hydrodynamic interactions which are efficiently screened in our system due to the fact that the measurements were performed at high polymer concentrations, i.e. in the semi-dilute regime. (letter to the editor)

Niobium Pentoxide thin films employ simple colloidal suspension at low preparation temperature

Directory of Open Access Journals (Sweden)

Abood M. K.

2017-01-01

Full Text Available In this work a nano-colloidal suspension is used to prepare Nb2O5 thin films. The effect of different substrates on structural properties of niobium pentoxide thin film deposited by spin coating technique on silicon and quartz substrates are presented. We observed that the obtained structure is monocline in both substrates. The diffraction peaks in both substrates ensured the successful formation of Nb2O5 thin films with a clear polymorphous structure. However, the structure became more crystalline with additional distinguished peaks on silicon substrate comparing to quartz substrate. The extracted structural parameters from X-Ray diffraction show that the grain size of the thin films on quartz is smaller than silicon with the values of 16.47 nm and 20.98 nm respectively. The stress measurement records the values of 0.19 and 0.00719 for the thin films deposited on silicon and quartz substrates respectively. Effects of film thickness depicted increment in the absorbance and reduction in the band gap. Energy gaps of 2.7, 2.58 and, 2.5 eV are measured as a result of increasing the film thicknesses of 325, 420 and 450 nm respectively.

Dynamics and Rheology of Soft Colloidal Glasses

KAUST Repository

Wen, Yu Ho

2015-01-20

© 2015 American Chemical Society. The linear viscoelastic (LVE) spectrum of a soft colloidal glass is accessed with the aid of a time-concentration superposition (TCS) principle, which unveils the glassy particle dynamics from in-cage rattling motion to out-of-cage relaxations over a broad frequency range 10-13 rad/s < ω < 101 rad/s. Progressive dilution of a suspension of hairy nanoparticles leading to increased intercenter distances is demonstrated to enable continuous mapping of the structural relaxation for colloidal glasses. In contrast to existing empirical approaches proposed to extend the rheological map of soft glassy materials, i.e., time-strain superposition (TSS) and strain-rate frequency superposition (SRFS), TCS yields a LVE master curve that satis fies the Kramers-Kronig relations which interrelate the dynamic moduli for materials at equilibrium. The soft glassy rheology (SGR) model and literature data further support the general validity of the TCS concept for soft glassy materials.

Experimental evidence of colloids and nanoparticles presence from 25 waste leachates

Energy Technology Data Exchange (ETDEWEB)

Hennebert, Pierre, E-mail: pierre.hennebert@ineris.fr [INERIS – Institut National de l’Environnement Industriel et des Risques, Domaine du Petit Arbois BP33, F-13545 Aix-en-Provence (France); Avellan, Astrid; Yan, Junfang [INERIS – Institut National de l’Environnement Industriel et des Risques, Domaine du Petit Arbois BP33, F-13545 Aix-en-Provence (France); Aguerre-Chariol, Olivier [INERIS, Parc Technologique ALATA, BP No. 2, 60550 Verneuil en Halatte (France)

2013-09-15

Highlights: • This work is the first assessment of colloids in waste leachates. • Analytical methods are proposed and discussed. • All the waste have at least one element in colloidal form, and some elements are always colloidal. • Man-made nanoparticles are observed. • It can change the interpretation of leachate elemental concentration. - Abstract: The potential colloids release from a large panel of 25 solid industrial and municipal waste leachates, contaminated soil, contaminated sediments and landfill leachates was studied. Standardized leaching, cascade filtrations and measurement of element concentrations in the microfiltrate (MF) and ultrafiltrate (UF) fraction were used to easily detect colloids potentially released by waste. Precautions against CO{sub 2} capture by alkaline leachates, or bacterial re-growth in leachates from wastes containing organic matter should be taken. Most of the colloidal particles were visible by transmission electron microscopy with energy dispersion spectrometry (TEM–EDS) if their elemental MF concentration is greater than 200 μg l{sup −1}. If the samples are dried during the preparation for microscopy, neoformation of particles can occur from the soluble part of the element. Size distribution analysis measured by photon correlation spectroscopy (PCS) were frequently unvalid, particularly due to polydispersity and/or too low concentrations in the leachates. A low sensitivity device is required, and further improvement is desirable in that field. For some waste leachates, particles had a zeta potential strong enough to remain in suspension. Mn, As, Co, Pb, Sn, Zn had always a colloidal form (MF concentration/UF concentration > 1.5) and total organic carbon (TOC), Fe, P, Ba, Cr, Cu, Ni are partly colloidal for more than half of the samples). Nearly all the micro-pollutants (As, Ba, Co, Cr, Cu, Mo, Ni, Pb, Sb, Sn, V and Zn) were found at least once in colloidal form greater than 100 μg l{sup −1}. In particular

Relations between fatty acid synthesis, pyruvate concentration and cell concentration of suspensions of isolated rat hepatocytes

NARCIS (Netherlands)

Beynen, A.C.; Geelen, M.J.H.

1984-01-01

1. 1. The cell concentration of suspensions of isolated rat hepatocytes affects both the rate of pyruvate accumulation in the incubation medium and the rate of fatty acid synthesis. 2. 2. At low cell concentrations pyruvate accumulation is directly related to the cell concentration but levels off

Rheology of dense suspensions of non colloidal particles

OpenAIRE

Guazzelli , Elisabeth

2017-01-01

International audience; Dense suspensions are materials with broad applications both in industrial processes (e.g. waste disposal, concrete, drilling muds, metalworking chip transport, and food processing) and in natural phenomena (e.g. flows of slurries, debris, and lava). Despite its long research history and its practical relevance, the mechanics of dense suspensions remain poorly understood. The major difficulty is that the grains interact both by hydrodynamic interactions through the liq...

Chain Dynamics in Magnetorheological Suspensions

Science.gov (United States)

Gast, A. P.; Furst, E. M.

1999-01-01

Magnetorheological (MR) suspensions are composed of colloidal particles which acquire dipole moments when subjected to an external magnetic field. At sufficient field strengths and concentrations, the dipolar particles rapidly aggregate to form long chains. Subsequent lateral cross-linking of the dipolar chains is responsible for a rapid liquid-to-solid-like rheological transition. The unique, magnetically-activated rheological properties of MR suspensions make them ideal for interfacing mechanical systems to electronic controls. Additionally, the ability to experimentally probe colloidal suspensions interacting through tunable anisotropic potentials is of fundamental interest. Our current experimental work has focused on understanding the fluctuations of dipolar chains. It has been proposed by Halsey and Toor (HT) that the strong Landau-Peierls thermal fluctuations of dipolar chains could be responsible for long-range attractions between chains. Such interactions will govern the long-time relaxation of MR suspensions. We have synthesized monodisperse neutrally buoyant MR suspensions by density matching stabilized ferrofluid emulsion droplets with D2O. This allows us to probe the dynamics of the dipolar chains using light scattering without gravitational, interfacial, and polydispersity effects to resolve the short-wavelength dynamics of the dipolar chains. We used diffusing wave spectroscopy to measure these dynamics. The particle displacements at short times that show an independence to the field strength, but at long times exhibit a constrained, sub-diffusive motion that slows as the dipole strength is increased. The experiments are in good qualitative agreement with Brownian dynamics simulations of dipolar chains. Although there have been several important and detailed studies of the structure and interactions in MR suspensions, there has not been conclusive evidence that supports or contradicts the HT model prediction that long-range interactions exist between

Rheology of dense suspensions of non colloidal particles

OpenAIRE

Guazzelli Élisabeth

2017-01-01

Dense suspensions are materials with broad applications both in industrial processes (e.g. waste disposal, concrete, drilling muds, metalworking chip transport, and food processing) and in natural phenomena (e.g. flows of slurries, debris, and lava). Despite its long research history and its practical relevance, the mechanics of dense suspensions remain poorly understood. The major difficulty is that the grains interact both by hydrodynamic interactions through the liquid and by mechanical co...

Injection of colloidal size particles of Fe0 in porous media with shearthinning fluids as a method to emplace a permeable reactive zone

International Nuclear Information System (INIS)

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

1997-01-01

Previous work has demonstrated the feasibility of injecting suspensions of micron-size zero-valent (FeO) particles into porous media as a method to emplace a permeable reactive zone. Further studies were conducted to evaluate the effects of several shearthinning fluids on enhancing the injectability of micron-size FeO particles into porous media. In contrast to Newtonian fluids, whose viscosities are constant with shear rate, certain non-Newtonian fluids are shearthinning, that is, the viscosity of these fluids decreases with increasing shear rate. The primary benefit of using these fluids for this application is that they increase the viscosity of the aqueous phase without adversely decreasing the hydraulic conductivity. A suspension formulated with a shearthinning fluid will maintain a relatively high viscosity in solution near the FeO particles (where the shear stress is low) relative to locations near the surfaces of the porous media, where the shear stress is high. The increased viscosity decreases the rate of gravitational settling of the dense FeO colloids (7.6 9/cm3) while maintaining a relatively high hydraulic conductivity that permits pumping the colloid suspensions into porous media at greater flowrates and distances. Aqueous solutions of three polymers at different concentrations were investigated. It was determined that, the use of shear thinning fluids greatly increases the injectability of the colloidal FeO suspensions in porous media

Influence of vibration on structure rheological properties of a highly concentrated suspension

Science.gov (United States)

Ouriev Uriev, Boris N.; Uriev, Naum B.

2005-08-01

The influence of mechanical vibration on the flow properties of a highly concentrated multiphase food system is explored in this work. An experimental set-up was designed and adapted to a conventional rotational rheometer with precise rheological characterization capability. A number of calibration tests were performed prior to fundamental experiments with a highly concentrated chocolate suspension. Also, the prediction of wall slippage in shear flow under vibration was evaluated. Analysis of the boundary conditions shows that no side effects such as wall slippage or the Taylor effect were present during the shear experiment under vibration. It was found that superposition of mechanical vibration and shear flow radically decreases the shear viscosity. Comparison between reference shear viscosities at specified shear rates and those measured under vibration shows considerable differences in flow properties. Conversion of the behaviour of the concentrated suspension from strongly shear-thinning to Newtonian flow is reported. Also, the appearance of vibration-induced dilatancy as a new phenomenon is described. It is suggested to relate such phenomena to the non-equilibrium between structure formation and disintegration under vibration and hydrodynamic forces of shear flow. The influence of vibration on structure formation can be well observed during measurement of the yield value of the chocolate suspension under vibration. Comparison with reference data shows how sensitive the structure of the concentrated suspension is to vibration in general. The effects and observations revealed provide a solid basis for further fundamental investigations of structure formation regularities in the flow of any highly concentrated system. The results also show the technological potential for non-conventional treatment of concentrated, multiphase systems.

Electric-surface characteristics and stability of type K coal suspensions

Energy Technology Data Exchange (ETDEWEB)

Baichenko, A A; Baran, A A; Mitina, N S; Kocherga, I I

1987-07-01

Investigates with the help of potentiometric titration, electrophoresis and conductometry the structure of double electric layer and aggregation stability of type K coal suspension at the Berezovsk preparation plant (Kuzbassugol' association). Discusses tests carried out with coal which was preliminarily crushed, sieved, crushed again in colloid mills, elutriated and separated into sedimento-stable fractions. Data obtained indicate that coal suspensions represent typical ion-stabilized dispersions, coagulation of which by electrolytes can be depicted within the framework of lyophobic colloid stability theory. Addition of double-charged gegenions considerably reduces electrokinetic potential while addition of triple-charged gegenions results in surface recharging. 10 refs.

Exploration and characterization of new synthesis methods for C60 colloidal suspensions in water

Science.gov (United States)

Hilburn, Martha E.

Buckminsterfullerene, C60, has been used in the production of several commercial products from badminton racquets and lubricants for their mechanical properties to cosmetics and even dietary supplements for their "antioxidant" properties. Multi-ton production of C60 began in 2003 encouraging serious consideration of its fate in the environment in the case of an accidental release or improper disposal. Although C60 is practically insoluble in water, it readily forms stable aqueous colloidal suspensions (termed nC60) through solvent exchange methods or long-term vigorous stirring in water. Two new solvent exchange methods for synthesizing nC60 are presented. These methods combine key advantages of multiple existing synthesis methods including high yield, narrow particle size distribution, short synthesis time, and an absence of solvents such as tetrahydrofuran that have historically caused problems in laboratory synthesized aggregates. The resulting samples are attractive candidates for use in controlled environmental impact, biological, and toxicity studies. An improved method for quantifying residual solvents in nC60 samples utilizing solid phase micro extraction gas chromatography mass spectrometry (SPME-GC-MS) is also discussed.

Flocking ferromagnetic colloids.

Science.gov (United States)

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

2017-02-01

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).

Scattering from correlations in colloidal systems

International Nuclear Information System (INIS)

Hayter, J.B.

1984-01-01

Colloidal suspensions typically exhibit spatial correlations over distances of order 10-10 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 -8 -10 -3 sec) than those found in simple atomic or small molecular systems (10 -13 -10 -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

Association behaviour of 241Am(III) on SiO2(amorphous) and SiO2(quartz) colloids

International Nuclear Information System (INIS)

Degueldre, C.; Wernli, B.

1993-01-01

SiO 2 colloids have been identified as a potential vector for enhancing radionuclide transport in granitic groundwater and in concrete pore water. The sorption behaviour of 241 Am(III) on SiO 2 colloids was studied as a function of americium concentration pH (5-12), colloid concentration, ionic strength, temperature and SiO 2 allotropic species. The Am(III) sorption mechanism on amorphous silica is different from that on quartz. For SiO 2(amorphous) solution, the variation of log K p (ml g -1 ) with pH is linear (pH=5-9) with a slope of +1 indicating a one proton exchange mechanism. The colloid concentration (ppm) affects the sorption and log K p 3.7-0.67 log [SiO 2 ] (pH = 6). K p increases insignificantly when the ionic strength decreases. It shows no significant variation, however, with the Am concentration. On amorphous silica, the Am(III) sorption is driven by proton exchange from the silanol groups. For SiO 2 (quartz), log K p is constant over a large range of quartz concentration in suspension and the variation of log K p with pH is about linear (pH = 5-12), with a slope of 0.28, indicating a more complex exchange mechanism. Reactions taking into account the interaction of positive Am(OH) w (3-w)+ species on to the negatively charged quartz surface are suggested. (author)

Sorption of microamount of colloidal silver iodide on hydrated iron(III) oxide

International Nuclear Information System (INIS)

Kepak, F.; Nova, J.

1975-01-01

Sorption of a microamount of colloidal silver iodide labelled with 131 I on hydrated iron/III/ oxide suspension was studied. The sorption dependence upon pH, sorbent amount, and inert electrolyte concentration has revealed that sorption of silver iodide reaches no more than 63%. The sorption lasted one hour during which the maximum value was reached. Desorption time was one hour, as well. Except for measuring the sorption dependence on pH, the sorption pH was 7.0, temperature 24+-2 0 C. (F.G.)

Size, velocity, and concentration in suspension measurements of spherical droplets and cylindrical jets.

Science.gov (United States)

Onofri, F; Bergougnoux, L; Firpo, J L; Misguich-Ripault, J

1999-07-20

The principle of an optical technique for simultaneous velocity, size, and concentration in suspension measurements of spherical droplets and cylindrical jets is proposed. This technique is based on phase Doppler anemometry working in the dual burst technique configuration. The particle size and velocity are deduced from the reflected signal phase and frequency, whereas the amplitude ratio between the refracted and the reflected signals is used for measuring the concentration of small scatterers inside the particles. Numerical simulations, based on geometrical optics and a Monte Carlo model, and an experimental validation test on cylindrical jets made of various suspensions, are used to validate the principle of the proposed technique. It is believed that this new technique could be useful in investigating processes in which liquid suspensions are sprayed for surface coating, drying, or combustion applications.

Self-Suspended Suspensions of Covalently Grafted Hairy Nanoparticles

KAUST Repository

Choudhury, Snehashis; Agrawal, Akanksha; Kim, Sung A; Archer, Lynden A.

2015-01-01

length scales. On mesoscopic length scales, the suspensions display exceptional homogeneity and colloidal stability. We attribute this feature to steric repulsions between grafted chains and the space-filling constraint on the tethered chains

Colloid properties in groundwaters from crystalline formations

International Nuclear Information System (INIS)

Degueldre, C.A.

1994-09-01

Colloids are present in all groundwaters. The role they may play in the migration of safety-relevant radionuclides in the geosphere therefore must be studied. Colloid sampling and characterisation campaigns have been carried out in Switzerland. On the bases of the results from studies in the Grimsel area, Northern Switzerland and the Black Forest, as well as those obtained by other groups concerned with crystalline waters, a consistent picture is emerging. The groundwater colloids in crystalline formations are predominantly comprised of phyllosilicates and silica originating from the aquifer rock. Under constant hydrogeochemical conditions, the colloid concentration is not expected to exceed 100 ng.ml -1 when the calcium concentration is greater than 10 -4 . However, under transient chemical or physical conditions, such as geothermal or tectonic activity, colloid generation may be enhanced and the colloid concentration may reach 10 μg.ml -1 or more, if both the calcium and sodium concentrations are low. In the Nagra Crystalline Reference Water the expected colloid concentration is -1 . This can be compared, for example, to a colloid concentration of about 10 ng.ml -1 found in Zurzach water. The small colloid concentration in the reference water is a consequence of an attachment factor for clay colloids (monmorillonite) close to 1. A model indicates that at pH 8, the nuclide partition coefficients between water and colloid (K p ) must be smaller than 10 7 ml.g -1 if sorption takes place by surface complexation on colloids, = AIOH active groups forming the dominant sorption sites. This pragmatic model is based on the competition between the formation of nuclide hydroxo complexes in solution and their sorption on colloids. Experimental nuclide sorption data on colloids are compared with those obtained by applying this model. For a low colloid concentration, a sorption capacity of the order of 10 -9 M and reversible surface complexation, their presence in the

Colloidal silver fabrication using the spark discharge system and its antimicrobial effect on Staphylococcus aureus.

Science.gov (United States)

Tien, Der-Chi; Tseng, Kuo-Hsiung; Liao, Chih-Yu; Tsung, Tsing-Tshih

2008-10-01

Nanoscale techniques for silver production may assist the resurgence of the medical use of silver, especially given that pathogens are showing increasing resistance to antibiotics. Traditional chemical synthesis methods for colloidal silver (CS) may lead to the presence of toxic chemical species or chemical residues, which may inhibit the effectiveness of CS as an antibacterial agent. To counter these problems a spark discharge system (SDS) was used to fabricate a suspension of colloidal silver in deionized water with no added chemical surfactants. SDS-CS contains both metallic silver nanoparticles (Ag(0)) and ionic silver forms (Ag(+)). The antimicrobial affect of SDS-CS on Staphylococcus aureus was studied. The results show that CS solutions with an ionic silver concentration of 30 ppm or higher are strong enough to destroy S. aureus. In addition, it was found that a solution's antimicrobial potency is directly related to its level of silver ion concentration.

Generation of colloidal granules and capsules from double emulsion drops

Science.gov (United States)

Hess, Kathryn S.

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

Microfluidic Fabrication Solutions for Tailor-Designed Fiber Suspensions

Directory of Open Access Journals (Sweden)

Helene Berthet

2016-11-01

Full Text Available Fibers are widely used in different industrial processes, for example in paper manufacturing or lost circulation problems in the oil industry. Recently, interest towards the use of fibers at the microscale has grown, driven by research in bio-medical applications or drug delivery systems. Microfluidic systems are not only directly relevant for lab-on-chip applications, but have also proven to be good model systems to tackle fundamental questions about the flow of fiber suspensions. It has therefore become necessary to provide fiber-like particles with an excellent control of their properties. We present here two complementary in situ methods to fabricate controlled micro-fibers allowing for an embedded fabrication and flow-on-a-chip platform. The first one, based on a photo-lithography principle, can be used to make isolated fibers and dilute fiber suspensions at specific locations of interest inside a microchannel. The self-assembly property of super-paramagnetic colloids is the principle of the second fabrication method, which enables the fabrication of concentrated suspensions of more flexible fibers. We propose a flow gallery with several examples of fiber flow illustrating the two methods’ capabilities and a range of recent laminar flow results.

Bletilla colloid as a vascular embolization agent: experimental studies

International Nuclear Information System (INIS)

Zheng Chuansheng; Feng Gansheng; Zhang Yanfang

1998-01-01

Purpose: To study the efficacy, safety and related characteristics of bletilla colloid as a vascular embolization agent. Materials and methods: The authors prepared bletilla colloid as a vascular embolization agent from the stem tubers of bletilla of Chinese medicinal herb. Related characteristics of bletilla colloid were studied. In four pigs hepatic arterial embolization was performed with the bletilla colloid. Results: The bletilla colloid was a homogenous viscous colloid whose relative viscosity was 2324.6 mm 2 /s. It was easily injected through 4-F catheter and hyperattenuating under fluoroscopy, meanwhile, with good histocompatibility and hemo-compatibility, without pyrogenetic response and toxicity. In vitro, the mixture of bletilla colloid and MMC did not produce separation and suspension phenomena but released 50% of MMC at 1.8h and 100% at 3.4h. The bletilla colloid mainly embolized peripheral arteries, maintaining occlusion for 5 weeks and without formation of collateral circulation. The injuries of normal hepatic tissues were slight, without hepatic cytonecrosis. Conclusions: Bletilla colloid, safe and effective in use with angioembolic function and characteristics of carrier and slow-release, is a potential peripheral embolization agent

Development of a Fabrication Process Using Suspension Plasma Spray for Titanium Oxide Photovoltaic Device

Directory of Open Access Journals (Sweden)

Hsian Sagr Hadi A

2017-03-01

Full Text Available In order to reduce the high costs of conventional materials, and to reduce the power necessary for the deposition of titanium dioxide, titanium tetrabutoxide has been developed in the form of a suspension of TiO2 using water instead of expensive ethanol. To avoid sedimentation of hydroxide particles in the suspension, mechanical milling of the suspension was conducted in order to create diffusion in colloidal suspension before using it as feedstock. Consequently, through the creation of a colloidal suspension, coating deposition was able to be conducted without sedimentation of the hydroxide particles in the suspension during the deposition process. Though an amorphous as-deposited coating was able to be deposited, through post heat treatment at 630 °C for 60 min, the chemical structure became anatase rich. In addition, it was confirmed that the post heat treated anatase rich coating had enough photo-catalytic activity to decolor methylene-blue droplets. From these results, this technique was found to have high potential in the low cost photo-catalytic titanium coating production process.

Manipulating semiconductor colloidal stability through doping.

Science.gov (United States)

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.

EDITORIAL: Colloidal dispersions in external fields Colloidal dispersions in external fields

Science.gov (United States)

Löwen, Hartmut

2012-11-01

third conference in a series that began in 2004 [2] and was continued in 2008 [3]. The CODEF meeting series is held in conjunction with the German Dutch Transregional Collaborative Research Centre SFB TR6 with the title Physics of Colloidal Dispersions in External Fields. Papers from scientists working within this network as well as those from further invited contributors are summarized in this issue. They are organized according to the type of field applied, namely: shear flow electric field laser-optical and magnetic field confinement other fields and active particles To summarize the highlights of this special issue as regards shear fields, the response of depletion-induced colloidal clusters to shear is explored in [4]. Soft particles deform under shear and their structural and dynamical behaviour is studied both by experiment [5] and theory [6]. Transient dynamics after switching on shear is described by a joint venture of theory, simulation and experiment in [7]. Colloids provide the fascinating possibility to drag single particles through the suspension, which gives access to microrheology (as opposed to macrorheology, where macroscopic boundaries are moved). Several theoretical aspects of microrheology are discussed in this issue [8-10]. Moreover, a microscopic theory for shear viscosity is presented [11]. Various aspects of colloids in electric fields are also included in this issue. Electrokinetic phenomena for charged suspensions couple flow and electric phenomena in an intricate way and are intensely discussed both by experiment and simulation in contributions [12-14]. Dielectric phenomena are also influenced by electric fields [15]. Electric fields can induce effective dipolar forces between colloids leading to string formation [16]. Finally, binary mixtures in an electric driving field exhibit laning [17]. Simulation [18] and theoretical [19] studies of this nonequilibrium phenomenon are also discussed in this issue. Laser-optical fields can be used to

Colloidal spray method for low cost thin coating deposition

Science.gov (United States)

Pham, Ai-Quoc; Glass, Robert S.; Lee, Tae H.

2002-01-01

A dense or porous coating of material is deposited onto a substrate by forcing a colloidal suspension through an ultrasonic nebulizer and spraying a fine mist of particles in a carrier medium onto a sufficiently heated substrate. The spraying rate is essentially matched to the evaporation rate of the carrier liquid from the substrate to produce a coating that is uniformly distributed over the surface of the substrate. Following deposition to a sufficient coating thickness, a single sintering step may be used to produce a dense ceramic coating. Using this method, coatings ranging in thickness from about one to several hundred microns can be obtained. By using a plurality of compounds in the colloidal suspension, coatings of mixed composition can be obtained. By using a plurality of solutions and separate pumps and a single or multiple ultrasonic nebulizer(s), and varying the individual pumping rates and/or the concentrations of the solutions, a coating of mixed and discontinuously graded (e.g., stepped) or continuously graded layers may be obtained. This method is particularly useful for depositing ceramic coatings. Dense ceramic coating materials on porous substrates are useful in providing improved electrode performance in devices such as high power density solid oxide fuel cells. Dense ceramic coatings obtained by the invention are also useful for gas turbine blade coatings, sensors, steam electrolyzers, etc. The invention has general use in preparation of systems requiring durable and chemically resistant coatings, or coatings having other specific chemical or physical properties.

The non-monotonic shear-thinning flow of two strongly cohesive concentrated suspensions

OpenAIRE

Buscall, Richard; Kusuma, Tiara E.; Stickland, Anthony D.; Rubasingha, Sayuri; Scales, Peter J.; Teo, Hui-En; Worrall, Graham L.

2014-01-01

The behaviour in simple shear of two concentrated and strongly cohesive mineral suspensions showing highly non-monotonic flow curves is described. Two rheometric test modes were employed, controlled stress and controlled shear-rate. In controlled stress mode the materials showed runaway flow above a yield stress, which, for one of the suspensions, varied substantially in value and seemingly at random from one run to the next, such that the up flow-curve appeared to be quite irreproducible. Th...

Rheological properties of ceramic nanopowders in aqueous and nonaqueous suspensions

International Nuclear Information System (INIS)

Tomaszewski, H.; Loiko, E.M.

2003-01-01

The potential for ceramic nanocomposites to offer significantly enhanced mechanical properties is generally known since the first work of Niihara published in 1991. However achieving these properties needs carefully done colloidal processing, because ceramic nanopowders are naturally prone to agglomeration. The work presented here is concerned with the processing of zirconia/alumina nanocomposites via aqueous and alumina silicon carbide nanocomposites via nonaqueous colloidal route. The effect of pH of aqueous alumina and zirconia suspensions on properties of suspension and centrifuged green bodies was studied. A correlation between surface electric charge of grains (zeta potential)and agglomerate size, viscosity of suspension and porosity of green compacts was found. In the case of nonaqueous route alumina and silicon carbide suspensions in iso-propanol were investigated. Electrostatic surface charge of grains was changed by addition of chloroacetic acid and determined indirectly by the mass of powder deposited on electrode during electrophoresis. Different behaviour of SiC nanopowder than of alumina was observed and mechanism of charge creation is proposed on the base of DLVO theory. The effect of grain charge on preventing agglomeration on the silicon carbide powder is presented on micrographs of sintered nanocomposites. (author)

Temperature-Triggered Colloidal Gelation through Well-Defined Grafted Polymeric Surfaces

Directory of Open Access Journals (Sweden)

Jan Maarten van Doorn

2017-06-01

Full Text Available Sufficiently strong interparticle attractions can lead to aggregation of a colloidal suspension and, at high enough volume fractions, form a mechanically rigid percolating network known as a colloidal gel. We synthesize a model thermo-responsive colloidal system for systematically studying the effect of surface properties, grafting density and chain length, on the particle dynamics within colloidal gels. After inducing an attraction between particles by heating, aggregates undergo thermal fluctuation which we observe and analyze microscopically; the magnitude of the variance in bond angle is larger for lower grafting densities. Macroscopically, a clear increase of the linear mechanical behavior of the gels on both the grafting density and chain length arises, as measured by rheology, which is inversely proportional to the magnitude of local bond angle fluctuations. This colloidal system will allow for further elucidation of the microscopic origins to the complex macroscopic mechanical behavior of colloidal gels including bending modes within the network.

Microrheology of colloidal systems

International Nuclear Information System (INIS)

Puertas, A M; Voigtmann, T

2014-01-01

Microrheology was proposed almost twenty years ago as a technique to obtain rheological properties in soft matter from the microscopic motion of colloidal tracers used as probes, either freely diffusing in the host medium, or subjected to external forces. The former case is known as passive microrheology, and is based on generalizations of the Stokes–Einstein relation between the friction experienced by the probe and the host-fluid viscosity. The latter is termed active microrheology, and extends the measurement of the friction coefficient to the nonlinear-response regime of strongly driven probes. In this review article, we discuss theoretical models available in the literature for both passive and active microrheology, focusing on the case of single-probe motion in model colloidal host media. A brief overview of the theory of passive microrheology is given, starting from the work of Mason and Weitz. Further developments include refined models of the host suspension beyond that of a Newtonian-fluid continuum, and the investigation of probe-size effects. Active microrheology is described starting from microscopic equations of motion for the whole system including both the host-fluid particles and the tracer; the many-body Smoluchowski equation for the case of colloidal suspensions. At low fluid densities, this can be simplified to a two-particle equation that allows the calculation of the friction coefficient with the input of the density distribution around the tracer, as shown by Brady and coworkers. The results need to be upscaled to agree with simulations at moderate density, in both the case of pulling the tracer with a constant force or dragging it at a constant velocity. The full many-particle equation has been tackled by Fuchs and coworkers, using a mode-coupling approximation and the scheme of integration through transients, valid at high densities. A localization transition is predicted for a probe embedded in a glass-forming host suspension. The

Grimsel colloid exercise

International Nuclear Information System (INIS)

Degueldre, C.; Longworth, G.; Vilks, P.

1989-11-01

The Grimsel Colloid Exercise was an intercomparison exercise which consisted of an in situ sampling phase followed by a colloid characterisation step. The goal of this benchmark exercise, which involved 12 laboratories, was to evaluate both sampling and characterisation techniques with emphasis on the colloid specific size distribution. The sampling phase took place at the Grimsel Test Site between February 1 and 13, 1988 and the participating groups produced colloid samples using the following methods: 1. Cross-flow ultrafiltration with production of membranes loaded with colloids. 2. Tangential diaultrafiltration and production of colloid concentrates. 3. Filtrates produced by each group. 4. Unfiltered water was also collected by PSI in glass bottles, under controlled anaerobic conditions, and by the other sampling groups in various plastic bottles. In addition, on-line monitoring of pH, χ, [O-2] and T of the water and of [O-2] in the atmosphere of the sampling units was carried out routinely. All samples were shipped according to the CoCo Club scheme for characterisation, with emphasis on the size distribution. The exercise differentiates the colloid samples produced on site from those obtained after transfer of the fluid samples to the laboratories. The colloid concentration and size distribution can be determined by scanning electron microscopy (SEM), gravimetry (GRAV), chemical analysis of fluid samples after micro/ultrafiltration (MF/UF) and by transmission single particle counting (PC). The colloid concentration can also be evaluated by transmission electron microscopy (TEM), static and dynamic light scattering (SLS,DLS) and by laser-induced photoacoustic spectroscopy (LPAS). The results are discussed on the basis of the detection limit, lateral resolution and counting conditions of the technique (precision) as well as sample preparation, artefact production and measurement optimisation (accuracy). A good agreement between size distribution results was

Characterization and Correlation of Particle-Level Interactions to the Macroscopic Rheology of Powders, Granular Slurries, and Colloidal Suspensions

Energy Technology Data Exchange (ETDEWEB)

A.P. Poloski; R.C. Daniel; D.R. Rector; P.R. Bredt; E.C. Buck; Berg, J.C.; Saez, A.E.

2006-09-29

This project had two primary objectives. The first was to understand the physical properties and behavior of select Hanford tank sludges under conditions that might exist during retrieval, treatment, packaging, and transportation for disposal at the Waste Isolation Pilot Plant (WIPP). The second objective was to develop a fundamental understanding of these sludge suspensions by correlating the macroscopic properties with particle interactions occurring at the colloidal scale. The specific tank wastes considered herein are contained in thirteen Hanford tanks including three double-shell tanks (DSTs) (AW-103, AW-105, and SY-102) and ten single-shell tanks (SSTs) (B-201 through B-204, T-201 through T-204, T-110, and T-111). At the outset of the project, these tanks were designated as potentially containing transuranic (TRU) process wastes that would be treated and disposed of in a manner different from the majority of the tank wastes.

Emulsions, foams, suspensions, and aerosols microscience and applications

CERN Document Server

Schramm, Laurier L

2014-01-01

This is the first book to provide an integrated introduction to the nature, formation and occurrence, stability, propagation, and uses of the most common types of colloidal dispersion in the process-related industries. The primary focus is on the applications of the principles, paying attention to practical processes and problems. This is done both as part of the treatment of the fundamentals, where appropriate, and also in the separate sections devoted to specifi c kinds of industries. Throughout, the treatment is integrated, with the principles of colloid and interface science common to each dispersion type presented for each major physical property class, followed by separate treatments of features unique to emulsions, foams, or suspensions. The first half of the book introduces the fundamental principles, introducing readers to suspension formation and stability, characterization, and fl ow properties, emphasizing practical aspects throughout. The following chapters discuss a wide range of industrial appl...

Crystallization in polydisperse colloidal suspensions

International Nuclear Information System (INIS)

Martin, S.; Bryant, G.; Van Megen, W.

2004-01-01

Full text: Crystallization and glass formation in colloidal hard spheres has been a very active area of research over the last 15-20 years. For most of this time particle polydispersity has been considered to be a minor concern in these studies. However, over the last few years an increasing number of simulations, theoretical work and experiments have shown that consideration of the polydispersity is critical in understanding these phenomena. In this paper we provide an overview of recent crystallization studies on particles with two very different particle size distributions. These particles exhibit very different equilibrium crystal structures and crystallization kinetics. Based on these measurements and time lapse photographs, we propose a growth mechanism whereby crystallization occurs in conjunction with a local fractionation process near the crystal-fluid interface, which significantly alters the kinetics of crystallite nucleation and growth. This fractionation effect becomes more significant as polydispersity or skewness increases. The unusual crystal structures observed are explained using a schematic model that explains the structure in terms of stacks of planes, which are unregistered due to a high incidence of stacking faults caused by the incorporation of a large number of small particles

Simulating the initial growth of a deposit from colloidal suspensions

International Nuclear Information System (INIS)

Oliveira, T J; Aarão Reis, F D A

2014-01-01

We study the short time properties of a two-dimensional film growth model in which incident particles execute advective-diffusive motion with a vertical step followed by D horizontal steps. The model represents some features of the deposition of anisotropic colloidal particles of the experiment of Yunker et al (2013 Phys. Rev. Lett. 110 035501), in which wandering particles are attracted to particle-rich regions in the deposit. Height profiles changing from rough to columnar structure are observed as D increases from 0 (ballistic deposition) to 8, with striking similarity to the experimental ones. The effective growth exponents match the experimental estimates and the scaling of those exponents on D shows a remarkable effect of the range of the particle-deposit interaction. The nearly ellipsoidal shape of colloidal particles is represented for the calculation of roughness exponents in conditions that parallel the experimental ones, giving a range of estimates that also includes the experimental values. The effective dynamic exponents calculated from the autocorrelation function are shown to be suitable to decide between a true dynamic scaling or transient behavior, particularly because the latter leads to deviations in an exponent relation. These results are consistent with arguments on short time unstable (columnar) growth of Nicoli et al (2013 Phys. Rev. Lett. 111 209601), indicating that critical quenched KPZ dynamics does not explain that colloidal particle deposition problem. (paper)

Green synthesis of highly concentrated aqueous colloidal solutions of large starch-stabilised silver nanoplatelets.

Science.gov (United States)

Cheng, Fei; Betts, Jonathan W; Kelly, Stephen M; Hector, Andrew L

2015-01-01

A simple, environmentally friendly and cost-effective method has been developed to prepare a range of aqueous silver colloidal solutions, using ascorbic acid as a reducing agent, water-soluble starch as a combined crystallising, stabilising and solubilising agent, and water as the solvent. The diameter of silver nanoplatelets increases with higher concentrations of AgNO3 and starch. The silver nanoparticles are also more uniform in shape the greater the diameter of the nanoparticles. Colloidal solutions with a very high concentration of large, flat, hexagonal silver nanoplatelets (~230 nm in breadth) have been used to deposit and fix an antibacterial coating of these large starch-stabilised silver nanoplates on commercial cotton fibres, using a simple dip-coating process using water as the solvent, in order to study the dependence of the antibacterial properties of these nanoplatelets on their size. Copyright © 2014 Elsevier B.V. All rights reserved.

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

Science.gov (United States)

Durham, Olivia Z.

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

Colloidal agglomerates in tank sludge: Impact on waste processing

International Nuclear Information System (INIS)

Bunker, B.C.; Martin, J.E.

1998-01-01

'Insoluble colloidal sludges in hazardous waste streams such as tank wastes can pose serious problems for waste processing, interfering with retrieval, transport, separation, and solidification procedures. Properties of sediment layers and sludge suspensions such as slurry viscosities, sedimentation rates, and final sediment densities can vary by orders of magnitude depending on the particle types present, the degree to which the particles agglomerate or stick to each other, and on a wide range of processing parameters such as solution shear rates, pH, salt content, and temperature. The objectives of this work are to: (1) understand the factors controlling the nature and extent of colloidal agglomeration under expected waste processing conditions; (2) determine how agglomeration phenomena influence physical properties relevant to waste processing including rheology, sedimentation, and filtration; and (3) develop strategies for optimizing processing conditions via control of agglomeration phenomena. Insoluble colloidal sludges in hazardous waste streams such as tank wastes can pose serious problems for waste processing, interfering with retrieval, transport, separation, and solidification procedures. Properties of sediment layers and sludge suspensions such as slurry viscosities, sedimentation rates, and final sediment densities can vary by orders of magnitude depending on the particle types present, the degree to which the particles agglomerate or stick to each other, and on a wide range of processing parameters such as solution shear rates, pH, salt content, and temperature. The objectives of this work are to: (1) understand the factors controlling the nature and extent of colloidal agglomeration under expected waste processing conditions; (2) determine how agglomeration phenomena influence physical properties relevant to waste processing including rheology, sedimentation, and filtration; and (3) develop strategies for optimizing processing conditions via control

Sampling and analysis of groundwater colloids. A literature review

International Nuclear Information System (INIS)

Takala, M.; Manninen, P.

2006-03-01

The purpose of this literature study was to give basic information of colloids: their formation, colloid material, sampling and characterisation of groundwater colloids. Colloids are commonly refereed to as particles in the size range of 1 nm to 1000 nm. They are defined as a suspension of solid material in a liquid that does not appear to separate even after a long period of time. Colloids can be formed from a variety of inorganic or organic material. Inorganic colloids in natural groundwaters are formed by physical fragmentation of the host rock or by precipitation. The water chemistry strongly controls the stability of colloids. The amount of colloid particles in a solution tends to decrease with the increasing ionic strength of the solution. Increases in pH and organic material tend to increase the stability of colloids. The mobility of colloids in a porous medium is controlled mainly by groundwater movement, sedimentation, diffusion and interception. Factors controlling sampling artefacts are oxygen diffusion: leads to e.g. calcite precipitation, pumping rates and filtering techniques. Efforts to minimise artefact formation should be taken if the scope of the sampling programme is to study the colloid particles. The colloid phase size distribution can be determined by light scattering systems, laser induced break down or by single particle analysis using SEM micrographs. Elemental compositions can be analysed with EDS spectrometry from single colloid particles. Bulk compositions of the colloid phase can be analysed with e.g. ICP-MS analyser. The results of this study can be used as guidelines for groundwater colloid samplings. Recommendations for future work are listed in the conclusions of this report. (orig.)

Technetium migration in Boom Clay - Assessing the role of colloid-facilitated transport in a deep clay formation

International Nuclear Information System (INIS)

Bruggeman, C.; Martens, E.; Maes, N.; Jacops, E.; Van Gompel, M.; Van Ravestyn, L.

2010-01-01

Document available in extended abstract form only. The role of colloids - mainly dissolved natural organic matter (NOM, 50-150 mg/l) - in the transport of radionuclides in the Boom Clay formation (Mol, Belgium), has long since been a matter of (heavy) debate. For more than 20 years, batch experiments with Boom Clay suspensions showed a pronounced influence of the dissolved organic carbon concentration on the aqueous concentrations of different radionuclides like Tc, Np, Am and U. Moreover, small fractions of these radionuclides were also observed to elute almost un-retarded out of confined clay cores in percolation experiments. In the past years, a new conceptual model for the speciation of the long-lived fission product Technetium- 99 ( 99 Tc) under Boom Clay conditions has been drafted. In brief, the stable oxidation state of 99 Tc in these conditions is +IV, and, therefore, Tc solution concentrations are limited by the solubility of TcO 2 .nH 2 O(s). However, during reduction of TcVII (in the TcO 4 - form) to TcIV, precursor TcO 2 .nH 2 O colloids are formed, which are stabilised by the dissolved organic matter present in Boom Clay interstitial pore water, and in supernatants of Boom Clay batch suspensions. Moreover, this stabilisation process occurs in such a systematic way, that (conditional) interaction constants could be established, and the behaviour was described as a 'hydrophobic sorption', or, more accurately, a 'colloid-colloid' interaction. This conceptual model was implemented into PHREEQC geochemical and Hydrus transport code to come to a reactive transport model that was used to simulate both the outflow and the tracer profile in several long-term running percolation experiments (both in lab and under in situ conditions). To account for slow dissociation kinetics of Tc from the NOM colloid, a first-order kinetic rate equation was also added to the model. In order to describe the migration of colloidal particles (NOM), an

Structure of Colloidal Flocs in relation to the Dynamic Properties of Unstable Suspension

Directory of Open Access Journals (Sweden)

Yasuhisa Adachi

2012-01-01

Full Text Available Dynamic behaviors of unstable colloidal dispersions are reviewed in terms of floc formation. Geometrical structure of flocs in terms of chemical conditions and formation mechanics is a key to predict macroscopic transportation properties. The rate of sedimentation and rheological properties can be described with the help of fractal dimension (D that is the function of the number of contacts between clusters (Nc. It is also well known that the application of water soluble polymers and polyelectrolytes, which are usually used as a conditioner or flocculants in colloidal dispersions, critically affects the process of flocculation. The resulted floc structure is also influenced by the application of polymer. In order to reveal the roles of the polymers, the elementary rate process of polymer reaching to colloidal interface and subsequent reconformation process into more stable adsorption state are needed to be analyzed. The properties of permeable flocs and adsorbed polymer (polyelectrolyte layers formed on the colloidal surfaces remain to be worked out in relation to inhomogeneous porous structure and electrokinetics in the future.

Optical filter based on Fabry-Perot structure using a suspension of goethite nanoparticles as electro-optic material

Science.gov (United States)

Abbas, Samir; Dupont, Laurent; Dozov, Ivan; Davidson, Patrick; Chanéac, Corinne

2018-02-01

We have investigated the feasibility of optical tunable filters based on a Fabry-Perot etalon that uses a suspension of goethite (α-FeOOH) nanorods as electro-optic material for application in optical telecommunications in the near IR range. These synthetic nanoparticles have a high optical anisotropy that give rise to a very strong Kerr effect in their colloidal suspensions. Currently, these particles are dispersed in aqueous solvent, with pH2 to ensure the colloidal electrostatic stability. However, the high conductivity of these suspensions requires using high-frequency electric fields (f > 1 MHz), which brings about a high power consumption of the driver. To decrease the field frequency, we have changed the solvent to ethylene glycol which has a lower electrical conductivity than the aqueous solvent. We have built a Fabry-Perot cell, filled with this colloidal suspension in the isotropic phase, and showed that a phase shift of 14 nm can be obtained in a field of 3V/μm. Therefore, the device can operate as a tunable filter. A key advantage of this filter is that it is, by principle, completely insensitive to the polarization of the input light. However, several technological issues still need to be solved, such as ionic contamination of the suspension from the blocking layers, and dielectrophoretic and thermal effects.

Sedimentation dynamics and equilibrium profiles in multicomponent mixtures of colloidal particles

International Nuclear Information System (INIS)

Spruijt, E; Biesheuvel, P M

2014-01-01

In this paper we give a general theoretical framework that describes the sedimentation of multicomponent mixtures of particles with sizes ranging from molecules to macroscopic bodies. Both equilibrium sedimentation profiles and the dynamic process of settling, or its converse, creaming, are modeled. Equilibrium profiles are found to be in perfect agreement with experiments. Our model reconciles two apparently contradicting points of view about buoyancy, thereby resolving a long-lived paradox about the correct choice of the buoyant density. On the one hand, the buoyancy force follows necessarily from the suspension density, as it relates to the hydrostatic pressure gradient. On the other hand, sedimentation profiles of colloidal suspensions can be calculated directly using the fluid density as apparent buoyant density in colloidal systems in sedimentation–diffusion equilibrium (SDE) as a result of balancing gravitational and thermodynamic forces. Surprisingly, this balance also holds in multicomponent mixtures. This analysis resolves the ongoing debate of the correct choice of buoyant density (fluid or suspension): both approaches can be used in their own domain. We present calculations of equilibrium sedimentation profiles and dynamic sedimentation that show the consequences of these insights. In bidisperse mixtures of colloids, particles with a lower mass density than the homogeneous suspension will first cream and then settle, whereas particles with a suspension-matched mass density form transient, bimodal particle distributions during sedimentation, which disappear when equilibrium is reached. In all these cases, the centers of the distributions of the particles with the lowest mass density of the two, regardless of their actual mass, will be located in equilibrium above the so-called isopycnic point, a natural consequence of their hard-sphere interactions. We include these interactions using the Boublik–Mansoori–Carnahan–Starling–Leland (BMCSL

Startup of electrophoresis in a suspension of colloidal spheres.

Science.gov (United States)

Chiang, Chia C; Keh, Huan J

2015-12-01

The transient electrophoretic response of a homogeneous suspension of spherical particles to the step application of an electric field is analyzed. The electric double layer encompassing each particle is assumed to be thin but finite, and the effect of dynamic electroosmosis within it is incorporated. The momentum equation for the fluid outside the double layers is solved through the use of a unit cell model. Closed-form formulas for the time-evolving electrophoretic and settling velocities of the particles in the Laplace transform are obtained in terms of the electrokinetic radius, relative mass density, and volume fraction of the particles. The time scale for the development of electrophoresis and sedimentation is significantly smaller for a suspension with a higher particle volume fraction or a smaller particle-to-fluid density ratio, and the electrophoretic mobility at any instant increases with an increase in the electrokinetic particle radius. The transient electrophoretic mobility is a decreasing function of the particle volume fraction if the particle-to-fluid density ratio is relatively small, but it may increase with an increase in the particle volume fraction if this density ratio is relatively large. The particle interaction effect in a suspension on the transient electrophoresis is much weaker than that on the transient sedimentation of the particles. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Colloidal stabilization of cerium-gadolinium oxide (CGO) suspensions via rheology

DEFF Research Database (Denmark)

Marani, Debora; Sudireddy, Bhaskar Reddy; Bentzen, Janet Jonna

2015-01-01

colloidally stable state. The method was applied to explore the ability of four commercial dispersants (acidic affine, neutral, basic affine, and polyvinylpyrrolidone (PVP)) to disperse cerium-gadolinium oxide (CGO) in ethanol. Only the acidic affine and the PVP dispersants were found to efficiently disperse...

Particle phase distribution of polycyclic aromatic hydrocarbons in stormwater — Using humic acid and iron nano-sized colloids as test particles

DEFF Research Database (Denmark)

Nielsen, Katrine; Kalmykova, Yuliya; Strömvall, Ann-Margret

2015-01-01

The distribution of polycyclic aromatic hydrocarbons (PAHs) in different particulate fractions in stormwater: Total, Particulate, Filtrated, Colloidal and Dissolved fractions, were examined and compared to synthetic suspensions of humic acid colloids and iron nano-sized particles. The distribution...

Superhydrophobic analyte concentration utilizing colloid-pillar array SERS substrates.

Science.gov (United States)

Wallace, Ryan A; Charlton, Jennifer J; Kirchner, Teresa B; Lavrik, Nickolay V; Datskos, Panos G; Sepaniak, Michael J

2014-12-02

The ability to detect a few molecules present in a large sample is of great interest for the detection of trace components in both medicinal and environmental samples. Surface enhanced Raman spectroscopy (SERS) is a technique that can be utilized to detect molecules at very low absolute numbers. However, detection at trace concentration levels in real samples requires properly designed delivery and detection systems. The following work involves superhydrophobic surfaces that have as a framework deterministic or stochastic silicon pillar arrays formed by lithographic or metal dewetting protocols, respectively. In order to generate the necessary plasmonic substrate for SERS detection, simple and flow stable Ag colloid was added to the functionalized pillar array system via soaking. Native pillars and pillars with hydrophobic modification are used. The pillars provide a means to concentrate analyte via superhydrophobic droplet evaporation effects. A ≥ 100-fold concentration of analyte was estimated, with a limit of detection of 2.9 × 10(-12) M for mitoxantrone dihydrochloride. Additionally, analytes were delivered to the surface via a multiplex approach in order to demonstrate an ability to control droplet size and placement for scaled-up uses in real world applications. Finally, a concentration process involving transport and sequestration based on surface treatment selective wicking is demonstrated.

Colloid-Colloid Hydrodynamic Interaction Around a Bend in a Quasi-One-Dimensional Channel

Science.gov (United States)

Liepold, Christopher; Zarcone, Ryan; Heumann, Tibor; Lin, Binhua; Rice, Stuart

We report a study of the correlation between a pair of particles in a colloid suspension in a bent quasi-one-dimensional (q1d) channel as a function of bend angle. As the bend angle becomes more acute, we observe an increasing depletion of particles in the vicinity of the bend and an increase in the nearest-neighbor separation in the pair correlation function for particles on opposite sides of the bend. Further, we observe that the peak value of D12, the coupling term in the pair diffusion tensor that characterizes the effect of the motion of particle 1 on particle 2, coincides with the first peak in the pair correlation function, and that the pair separation dependence of D12 mimics that of the pair correlation function. We show that the observed behavior is a consequence of the geometric constraints imposed by the single-file requirement that the particle centers lie on the centerline of the channel and the requirement that the hydrodynamic flow must follow the channel around the bend. We find that the correlation between a pair of particles in a colloidal suspension in a bent q1D channel has the same functional dependence on the pair correlation function as in a straight q1D channel when measured in a coordinate system that follows the centerline of the bent channel. NSF MRSEC (DMR-1420709), Dreyfus Foundation (SI-14-014).

Final Report: Model interacting particle systems for simulation and macroscopic description of particulate suspensions

Energy Technology Data Exchange (ETDEWEB)

Peter J. Mucha

2007-08-30

Suspensions of solid particles in liquids appear in numerous applications, from environmental settings like river silt, to industrial systems of solids transport and water treatment, and biological flows such as blood flow. Despite their importance, much remains unexplained about these complicated systems. Mucha's research aims to improve understanding of basic properties of suspensions through a program of simulating model interacting particle systems with critical evaluation of proposed continuum equations, in close collaboration with experimentalists. Natural to this approach, the original proposal centered around collaboration with studies already conducted in various experimental groups. However, as was detailed in the 2004 progress report, following the first year of this award, a number of the questions from the original proposal were necessarily redirected towards other specific goals because of changes in the research programs of the proposed experimental collaborators. Nevertheless, the modified project goals and the results that followed from those goals maintain close alignment with the main themes of the original proposal, improving efficient simulation and macroscopic modeling of sedimenting and colloidal suspensions. In particular, the main investigations covered under this award have included: (1) Sedimentation instabilities, including the sedimentation analogue of the Rayleigh-Taylor instability (for heavy, particle-laden fluid over lighter, clear fluid). (2) Ageing dynamics of colloidal suspensions at concentrations above the glass transition, using simplified interactions. (3) Stochastic reconstruction of velocity-field dependence for particle image velocimetry (PIV). (4) Stochastic modeling of the near-wall bias in 'nano-PIV'. (5) Distributed Lagrange multiplier simulation of the 'internal splash' of a particle falling through a stable stratified interface. (6) Fundamental study of velocity fluctuations in sedimentation

Rheological studies of aqueous stabilised nano-zirconia particle suspensions

Directory of Open Access Journals (Sweden)

Asad Ullah Khan

2012-02-01

Full Text Available In the present investigation aqueous suspensions of nano- and colloidal range particles are stabilised by changing the ambient pH. Rheology is used to establish the stability of the suspensions and it is found that the rheology of the suspensions is strongly dependent on the pH values. The viscosity is highest close to the iso-electric point of the powders. At the iso-electric point the net surface charge on the powder particles is zero and is the cause of the high viscosity. Away from the iso-electric point, the particles are charged, giving rise to a double layer phenomenon and causing the reduction in viscosity. It is also found that increasing the solid contents of the suspensions reduces the pH region of low viscosity.

Preparation of conjugated polymer suspensions by using ultrasonic atomizer

Energy Technology Data Exchange (ETDEWEB)

Tada, Kazuya, E-mail: tada@eng.u-hyogo.ac.jp; Onoda, Mitsuyoshi

2010-11-30

The electrophoretic deposition is a method useful to prepare conjugated polymer films for electronic devices. This method provides high material recovery rate on the substrate from the suspension, in contrast to the conventional spin-coating in which most of the material placed on the substrate is blown away. Although manual reprecipitation technique successfully yields suspensions of various conjugated polymers including polyfluorene derivatives, it is favorable to control the preparation process of suspensions. In this context, this paper reports preliminary results on the preparation of suspension of conjugated polymer by using an ultrasonic atomizer. While the resultant films do not show particular difference due to the preparation methods of the suspension, the electric current profiles during the electrophoretic deposition suggests that the ultrasonic atomization of polymer solution prior to be mixed with poor solvent results in smaller and less uniform colloidal particles than the conventional manual pouring method.

Actinide colloid generation in groundwater

International Nuclear Information System (INIS)

Kim, J.I.

1990-05-01

The progress made in the investigation of actinide colloid generation in groundwaters is summarized and discussed with particular examples relevant to an understanding of the migration behaviour of actinides in natural aquifer systems. The first part deals with the characterization of colloids: groundwater colloids, actinide real-colloids and actinide pseudocolloids. The second part concentrates on the generation processes and migration behaviour of actinide pseudocolloids, which are discussed with some notable experimental examples. Importance is stressed more on the chemical aspects of the actinide colloid generation in groundwater. This work is a contribution to the CEC project MIRAGE II, particularly, to research area: complexation and colloids. (orig.)

Determination of adsorbed protein concentration in aluminum hydroxide suspensions by near-infrared transmittance Spectroscopy

DEFF Research Database (Denmark)

Lai, Xuxin; Zheng, Yiwu; Jacobsen, Susanne

2008-01-01

, using the partial least square regression (PLSR) method to construct a calibration model. The linear concentration range of adsorbed BSA is from 0 to 1.75 mg/mL by using 10 mm path length cuvettes. The influence of the sedimentation in suspension, different buffers, and different aluminum hydroxide......Analysis of aluminum hydroxide based vaccines is difficult after antigen adsorption. Adsorbed protein is often assessed by measuring residual unadsorbed protein for quality control. A new method for the direct determination of adsorbed protein concentration in suspension using near-infrared (NIR......) transmittance spectroscopy is proposed here. A simple adsorption system using albumin from bovine serum (BSA) and aluminum hydroxide as a model system is employed. The results show that the NIR absorbance at 700-1300 nm is correlated to the adsorbed BSA concentration, measured by the ultraviolet (UV) method...

Separation process for very concentrated emulsions and suspensions in the food industry

NARCIS (Netherlands)

Dinther, van A.M.C.; Schroën, C.G.P.H.; Boom, R.M.

2013-01-01

Separation of concentrated food suspensions and emulsions by e.g. microfiltration is currently not possible and therefore preceded by dilution, wasting energy and water. A new approach is shown, with sieves having pores much larger than the micron-sized droplets, low cross-flow velocities and a

A splitting integration scheme for the SPH simulation of concentrated particle suspensions

Science.gov (United States)

Bian, Xin; Ellero, Marco

2014-01-01

Simulating nearly contacting solid particles in suspension is a challenging task due to the diverging behavior of short-range lubrication forces, which pose a serious time-step limitation for explicit integration schemes. This general difficulty limits severely the total duration of simulations of concentrated suspensions. Inspired by the ideas developed in [S. Litvinov, M. Ellero, X.Y. Hu, N.A. Adams, J. Comput. Phys. 229 (2010) 5457-5464] for the simulation of highly dissipative fluids, we propose in this work a splitting integration scheme for the direct simulation of solid particles suspended in a Newtonian liquid. The scheme separates the contributions of different forces acting on the solid particles. In particular, intermediate- and long-range multi-body hydrodynamic forces, which are computed from the discretization of the Navier-Stokes equations using the smoothed particle hydrodynamics (SPH) method, are taken into account using an explicit integration; for short-range lubrication forces, velocities of pairwise interacting solid particles are updated implicitly by sweeping over all the neighboring pairs iteratively, until convergence in the solution is obtained. By using the splitting integration, simulations can be run stably and efficiently up to very large solid particle concentrations. Moreover, the proposed scheme is not limited to the SPH method presented here, but can be easily applied to other simulation techniques employed for particulate suspensions.

Using Potentiometric Free Drug Sensors to Determine the Free Concentration of Ionizable Drugs in Colloidal Systems

DEFF Research Database (Denmark)

Tran, Thuy; Chakraborty, Anjan; Xi, Xi

2018-01-01

The present study investigates the use of free drug sensors (FDS) to measure free ionized drug concentrations in colloidal systems, including micellar solutions, emulsions, and lipid formulations during in vitro lipolysis. Diphenhydramine hydrochloride (DPH) and loperamide hydrochloride (LOP) wer...

Observations of the initial stages of colloidal band formation

Science.gov (United States)

Li, Yanrong; Tagawa, Yoshiyuki; Yee, Andrew; Yoda, Minami

2017-11-01

A number of studies have shown that particles suspended in a conducting fluid near a wall are subject to wall-normal repulsive ``lift'' forces, even in the absence of interparticle interactions, in a flowing suspension. Evanescent-wave visualizations have shown that colloidal particles in a dilute (volume fractions negative zeta-potentials. Above a minimum ``threshold'' electric field magnitude |Emin | , the particles assemble into dense ``bands'' with cross-sectional dimensions of a few μm and length comparable to that of the channel (i.e., a few cm). The results suggest that the threshold field |Emin | is large enough so that there is a region of ``reverse'' flow, along the direction of the EO flow, near the wall. Visualization of a large segment of the channel (>300 hydraulic diameters) at frame rates as great as 1 kHz is used to determine banding maps for a variety of dilute colloidal suspensions and to investigate the initial stages of band formation over a wide range of flow conditions. Supported by US Army Research Office.

Colloids from the aqueous corrosion of uranium nuclear fuel

Science.gov (United States)

Kaminski, M. D.; Dimitrijevic, N. M.; Mertz, C. J.; Goldberg, M. M.

2005-12-01

Colloids may enhance the subsurface transport of radionuclides and potentially compromise the long-term safe operation of the proposed radioactive waste repository at Yucca Mountain. Little data is available on colloid formation for the many different waste forms expected to be buried in the repository. This work expands the sparse database on colloids formed during the corrosion of metallic uranium nuclear fuel. We characterized spherical UO 2 and nickel-rich montmorilonite smectite-clay colloids formed during the corrosion of uranium metal fuel under bathtub conditions at 90 °C. Iron and chromium oxides and calcium carbonate colloids were present but were a minor population. The estimated upper concentration of the UO 2 and clays was 4 × 10 11 and 7 × 10 11-3 × 10 12 particles/L, respectively. However, oxygen eventually oxidized the UO 2 colloids, forming long filaments of weeksite K 2(UO 2) 2Si 6O 15 · 4H 2O that settled from solution, reducing the UO 2 colloid population and leaving predominantly clay colloids. The smectite colloids were not affected by oxygen. Plutonium was not directly observed within the UO 2 colloids but partitioned completely to the colloid size fraction. The plutonium concentration in the colloidal fraction was slightly higher than the value used in the viability assessment model, and does not change in concentration with exposure to oxygen. This paper provides conclusive evidence for single-phase radioactive colloids composed of UO 2. However, its impact on repository safety is probably small since oxygen and silica availability will oxidize and effectively precipitate the UO 2 colloids from concentrated solutions.

Improved sentinel node visualization in breast cancer by optimizing the colloid particle concentration and tracer dosage

NARCIS (Netherlands)

Valdés Olmos, R. A.; Tanis, P. J.; Hoefnagel, C. A.; Nieweg, O. E.; Muller, S. H.; Rutgers, E. J.; Kooi, M. L.; Kroon, B. B.

2001-01-01

Faint lymph uptake may hamper sentinel node (SN) identification by scintigraphy and subsequent gamma probe localization. The aim of the present study was to evaluate an adjustment in the colloid particle concentration and tracer dosage to optimize mammary lymphoscintigraphy. Scintigraphy was

Characterization, origin and aggregation behavior of colloids in eutrophic shallow lake.

Science.gov (United States)

Xu, Huacheng; Xu, Mengwen; Li, Yani; Liu, Xin; Guo, Laodong; Jiang, Helong

2018-05-31

Stability of colloidal particles contributes to the turbidity in the water column, which significantly influences water quality and ecological functions in aquatic environments especially shallow lakes. Here we report characterization, origin and aggregation behavior of aquatic colloids, including natural colloidal particles (NCPs) and total inorganic colloidal particles (TICPs), in a highly turbid shallow lake, via field observations, simulation experiments, ultrafiltration, spectral and microscopic, and light scattering techniques. The colloidal particles were characterized with various shapes (spherical, polygonal and elliptical) and aluminum-, silicon-, and ferric-containing mineralogical structures, with a size range of 20-200 nm. The process of sediment re-suspension under environmentally relevant conditions contributed 78-80% of TICPs and 54-55% of NCPs in Lake Taihu, representing an important source of colloids in the water column. Both mono- and divalent electrolytes enhanced colloidal aggregation, while a reverse trend was observed in the presence of natural organic matter (NOM). The influence of NOM on colloidal stability was highly related to molecular weight (MW) properties with the high MW fraction exhibiting higher stability efficiency than the low MW counterparts. However, the MW-dependent aggregation behavior for NCPs was less significant than that for TICPs, implying that previous results on colloidal behavior using model inorganic colloids alone should be reevaluated. Further studies are needed to better understand the mobility/stability and transformation of aquatic colloids and their role in governing the fate and transport of pollutants in natural waters. Copyright © 2018. Published by Elsevier Ltd.

Characterization of colloidal manganese hydroxylapatite: A potential magnetic resonance contrast agent

Science.gov (United States)

Dorshow, Richard B.; Kofi Adzamli, I.; Nosco, Dennis L.; Joslin, Frederick L.

1996-03-01

Particulate contrast agents for blood pool imaging need to be constructed with the appropriate particle size distribution (PSD), and need to be resistant to opsonization. Hence, the PSD of an aqueous colloidal suspension of polyethylene glycol (PEG)-stabilized manganese hydroxylapatite (potentially useful as a magnetic resonance contrast agent for blood pool imaging) has been investigated as a function of PEG concentration and molecular weight. At low PEG concentrations, dynamic light scattering (DLS) and sedimentation field flow fractionation measurements yield a broad PSD, with the largest particle diameters near 100nm. Flow field flow fractionation (FlFFF) measurements, however, yield a distinct population near 10nm, which is not readily detectable by the other two techniques. As the PEG concentration is increased, the PSD shifts toward the lower size population. At the highest PEG concentration employed, only particles of diameter 10nm remain, verified by both FlFFF and DLS. Thus, the search for an optimum PSD for blood pool imaging is facilitated by choice of PEG molecular weight and concentration, and by employing complementary use of light scattering and field flow fractionation techniques.

The colloid investigations conducted at the Aespoe Hard Rock Laboratory during 2000-2004

Energy Technology Data Exchange (ETDEWEB)

Laaksoharju, Marcus [Geopoint AB, Stockholm (Sweden); Wold, Susanna [Royal Inst. of Tech., Stockholm (Sweden). School of Chemical Science and Engineering, Nuclear Chemistry] (eds.)

2005-12-15

In 2000, SKB decided to initiate an international colloid project at the Aespoe Hard Rock Laboratory in Sweden. The objectives of the colloid project are to: (i) study the role of bentonite as a colloid source, (ii) verify the background colloid concentration at Aespoe HRL and, (iii) investigate the potential for colloid formation/transport in natural groundwater concentrations. The experimental concepts for the colloid project are: laboratory experiments with bentonite, background field measurements of natural colloids, borehole specific bentonite colloid stability experiments and a fracture specific transport experiment. The activities concerning the laboratory experiments and background field measurements are described in this work; the other activities are ongoing or planned. The following conclusions were made: The bentonite colloid stability is strongly dependent on the groundwater ionic strength. Natural colloids are organic degradation products such as humic and fulvic acids, inorganic colloids (clay, calcite, iron hydroxide) and microbes. Microbes form few but large particles and their concentration increase with increasing organic carbon concentrations. The small organic colloids are present in very low concentrations in deep granitic groundwater. The concentrations can be rather high in shallow waters. The colloid concentration decreases with depth and salinity, since colloids are less stable in saline waters. The colloid content at Aespoe is less than 300 ppb. The colloid content at repository level is less than 50 ppb. The groundwater variability obtained in the boreholes reflects well the natural groundwater variability along the whole HRL tunnel.

The colloid investigations conducted at the Aespoe Hard Rock Laboratory during 2000-2004

International Nuclear Information System (INIS)

Laaksoharju, Marcus; Wold, Susanna

2005-12-01

In 2000, SKB decided to initiate an international colloid project at the Aespoe Hard Rock Laboratory in Sweden. The objectives of the colloid project are to: (i) study the role of bentonite as a colloid source, (ii) verify the background colloid concentration at Aespoe HRL and, (iii) investigate the potential for colloid formation/transport in natural groundwater concentrations. The experimental concepts for the colloid project are: laboratory experiments with bentonite, background field measurements of natural colloids, borehole specific bentonite colloid stability experiments and a fracture specific transport experiment. The activities concerning the laboratory experiments and background field measurements are described in this work; the other activities are ongoing or planned. The following conclusions were made: The bentonite colloid stability is strongly dependent on the groundwater ionic strength. Natural colloids are organic degradation products such as humic and fulvic acids, inorganic colloids (clay, calcite, iron hydroxide) and microbes. Microbes form few but large particles and their concentration increase with increasing organic carbon concentrations. The small organic colloids are present in very low concentrations in deep granitic groundwater. The concentrations can be rather high in shallow waters. The colloid concentration decreases with depth and salinity, since colloids are less stable in saline waters. The colloid content at Aespoe is less than 300 ppb. The colloid content at repository level is less than 50 ppb. The groundwater variability obtained in the boreholes reflects well the natural groundwater variability along the whole HRL tunnel

Effect of solvent composition on dispersing ability of reaction sialon suspensions.

Science.gov (United States)

Xu, Xin; Oliveira, Marta; Ferreira, José M F

2003-03-15

This work focuses on the optimization of the rheological behavior of suspensions considering different solvent compositions. The effects of methyl ethyl ketone (MEK)/ethanol (E) solvent mixtures on reaction sialon suspensions were investigated by measuring sedimentation behavior, adsorption of dispersant, and flow behavior. It was shown that both the flow behavior and the sedimentation behavior strongly depended on selection of solvent composition. Using 3 wt% KD1 as dispersant, well-dispersed colloidal suspensions could be obtained in MEK-rich solvents. The suspensions with 60 vol% MEK/40 vol% E as solvent could be fitted to the Bingham model with very low yield stress, while suspensions with pure MEK or ethanol-rich mixtures as solvent showed pseudo plastic behavior with relatively high yield stress values. A model was proposed to explain the different flow behaviors of suspensions considering the different configurations of dispersant at particles' surfaces.

Magnetic Assisted Colloidal Pattern Formation

Science.gov (United States)

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

Granular-front formation in free-surface flow of concentrated suspensions

Science.gov (United States)

Leonardi, Alessandro; Cabrera, Miguel; Wittel, Falk K.; Kaitna, Roland; Mendoza, Miller; Wu, Wei; Herrmann, Hans J.

2015-11-01

A granular front emerges whenever the free-surface flow of a concentrated suspension spontaneously alters its internal structure, exhibiting a higher concentration of particles close to its front. This is a common and yet unexplained phenomenon, which is usually believed to be the result of fluid convection in combination with particle size segregation. However, suspensions composed of uniformly sized particles also develop a granular front. Within a large rotating drum, a stationary recirculating avalanche is generated. The flowing material is a mixture of a viscoplastic fluid obtained from a kaolin-water dispersion with spherical ceramic particles denser than the fluid. The goal is to mimic the composition of many common granular-fluid materials, such as fresh concrete or debris flow. In these materials, granular and fluid phases have the natural tendency to separate due to particle settling. However, through the shearing caused by the rotation of the drum, a reorganization of the phases is induced, leading to the formation of a granular front. By tuning the particle concentration and the drum velocity, it is possible to control this phenomenon. The setting is reproduced in a numerical environment, where the fluid is solved by a lattice-Boltzmann method, and the particles are explicitly represented using the discrete element method. The simulations confirm the findings of the experiments, and provide insight into the internal mechanisms. Comparing the time scale of particle settling with the one of particle recirculation, a nondimensional number is defined, and is found to be effective in predicting the formation of a granular front.

Confocal microscopy of colloidal dispersions in shear flow using a counter-rotating cone-plate shear cell

International Nuclear Information System (INIS)

Derks, Didi; Wisman, Hans; Blaaderen, Alfons van; Imhof, Arnout

2004-01-01

We report on novel possibilities for studying colloidal suspensions in a steady shear field in real space. Fluorescence confocal microscopy is combined with the use of a counter-rotating cone-plate shear cell. This allows imaging of individual particles in the bulk of a sheared suspension in a stationary plane. Moreover, this plane of zero velocity can be moved in the velocity gradient direction while keeping the shear rate constant. The colloidal system under study consists of rhodamine labelled PMMA spheres in a nearly density and refractive index matched mixture of cyclohexylbromide and cis-decalin. We show measured flow profiles in both the fluid and the crystalline phase and find indications for shear banding in the case of a sheared crystal. Furthermore, we show that, thanks to the counter-rotating principle of the cone-plate shear cell, a layer of particles in the bulk of a sheared crystalline suspension can be imaged for a prolonged time, with the result that their positions can be tracked

Sampling and characterisation of groundwater colloids in ONKALO at Olkiluoto, Finland, 2011

Energy Technology Data Exchange (ETDEWEB)

Takala, M.; Ojala, S.; Jarvinen, E.; Manninen, P. [Ramboll Finland Oy, Espoo (Finland)

2012-11-15

The purpose of this study was to estimate the concentration of colloids and composition of the colloid phase on the basis of the water chemistry results of filtered and unfiltered water samples and to compare the results with the previous ones. The water samples were collected from groundwater stations ONK-PVA1 and ONK-PVA3 in October 2011. The colloid concentrations were determined from scanning electron microscopy (SEM) micrographs taken from the filters. The change in the water chemistry due to filtration was also analysed. The decrease of element concentrations due to filtration would possibly reflect the composition of the colloid phase. Because the concentration of the colloids is very low, two parallel water samples were analysed five times with an Inductively Coupled Plasma - Mass Spectrometry (ICP-MS) analyser so that the chemical differences between the filtered and unfiltered water could be evaluated. The colloid concentration in ONK-PVA1, determined by the single particle analysis of SEM micrographs, was 6 {mu}g/l while the colloid concentration in ONK-PVA3 was 7 {mu}g/l. The colloid phase composition could not be reliably determined due to the low colloid concentration. (orig.)

Formation and stability of aluminosilicate colloids by coprecipitation

Energy Technology Data Exchange (ETDEWEB)

Putri, Kirana Yuniati

2011-02-15

Colloids are ubiquitous in natural waters. Colloid-facilitated migration is of importance in safety assessment of a nuclear waste disposal. Aluminosilicate colloids are considered to be the kernel of aquatic colloids. Their stability is affected by a number of geochemical parameters. This work aims to study qualitatively and quantitatively the stability of aluminosilicate colloids formed by coprecipitation under various geochemical conditions, i.e. pH, concentration of Al and Si metal ions, ionic strength, and omnipresent cations (Na{sup +}, Ca{sup 2+}, and Mg{sup 2+}). The work is performed by colorimetric method and laser-induced breakdown detection (LIBD). Two consecutive phase separations at 450 nm and 1 kDa are applied to separate the precipitates and colloids from the ionic species. By means of colorimetry, Si and Al can be detected down to 5.8 x10{sup -8} M and 7.4x10{sup -7} M, respectively. On the other hand, LIBD is able to quantify the colloidal size and its number density down to several ppt. Depending on the concentration of Al and Si metal ions, the formation trend of aluminosilicate colloid changes following its solubility curve. The lower the concentration, the higher the pH range in which the colloids start to emerge. Furthermore, the colloids are stable at higher Al and Si concentration and at low ionic strength. In the low pH range, cations provide different effects at low and high ionic strengths. At high ionic strength, the colloids are stable in the presence of a larger cation, while all cations exhibit similar effects at low ionic strength. However, in the high pH range, valence seems to have a stronger effect than ionic radius; colloids are more stable in the presence of monovalent cations than divalent ones. Meanwhile, XRD shows non- and/or poor crystalline structure of the aluminosilicate species. Nevertheless, results from XPS may suggest that the chemical composition (Si/Al ∼ 0.6) of the aluminosilicate precipitates is sillimanite or

Viscoelasticity and diffusional properties of colloidal model dispersions

International Nuclear Information System (INIS)

Naegele, Gerhard

2003-01-01

We examine linear viscoelastic, and translational and rotational diffusion properties of colloidal model dispersions. Theoretical results are discussed, in comparison with experiments, for monodisperse suspensions of charged and neutral colloidal spheres, and for binary dispersions of differently sized tracer and host particles. The theoretical methods employed comprise a mode-coupling scheme for Brownian particles, and a rooted cluster expansion scheme of tracer diffusion with two- and three-body hydrodynamic interactions included. We analyse in particular the validity of various empirical generalized Stokes-Einstein-Debye (SED) relations between the (dynamic) shear viscosity and translational/rotational diffusion coefficients. Some of these generalized SED relations are basic to microrheological measurements aimed at characterizing the viscoelasticity of complex fluids on the basis of the diffusional properties of immersed tracer particles

Viscoelasticity and diffusional properties of colloidal model dispersions

CERN Document Server

Naegele, G

2003-01-01

We examine linear viscoelastic, and translational and rotational diffusion properties of colloidal model dispersions. Theoretical results are discussed, in comparison with experiments, for monodisperse suspensions of charged and neutral colloidal spheres, and for binary dispersions of differently sized tracer and host particles. The theoretical methods employed comprise a mode-coupling scheme for Brownian particles, and a rooted cluster expansion scheme of tracer diffusion with two- and three-body hydrodynamic interactions included. We analyse in particular the validity of various empirical generalized Stokes-Einstein-Debye (SED) relations between the (dynamic) shear viscosity and translational/rotational diffusion coefficients. Some of these generalized SED relations are basic to microrheological measurements aimed at characterizing the viscoelasticity of complex fluids on the basis of the diffusional properties of immersed tracer particles.

Method to separate lignin-rich solid phase from acidic biomass suspension at an acidic pH

Science.gov (United States)

Yasarla, Kumar Lakshmi Rakesh; Ramarao, Bandaru V; Amidon, Thomas

2017-09-05

A method of separating a lignin-rich solid phase from a solution suspension, by pretreating a lignocellulosic biomass with a pretreatment fluid having remove soluble components, colloidal material and primarily lignin containing particles; separating the pretreated lignocellulosic biomass from the pretreatment fluid with soluble components, colloidal material and primarily lignin containing particles; flocculating the separated pretreatment fluid with soluble components, colloidal material and primarily lignin containing particles using polyethylene oxide (i.e., PEO) or cationic Poly acrylamide (i.e., CPAM) as a flocculating agent; and filtering the flocculated separated pretreatment fluid with soluble components, colloidal material and primarily lignin containing particles to remove agglomerates.

Injection molding of Y-TZP powders prepared by colloidal processing

International Nuclear Information System (INIS)

Kimura, Y.; Mineshita, O.; Kaga, T.; Tokinaga, T.; Obitsu, M.

1991-01-01

TZP powders containing 3mol% Y 2 O 3 were prepared from ZrOCl 2 solution via an aqueous colloidal suspension of ZrO 2 . Processing variables were optimized to obtain powders suitable for injection molding. Wettability of powders with binders, fluidity of melting compound, removal of binder from green body, and properties of sintered body were investigated

Actinide colloid generation in groundwater. Part 2

International Nuclear Information System (INIS)

Kim, J.I.

1991-01-01

The progress made in the investigation of actinide colloid generation in groundwater is summarized and discussed with particular examples relevant to an understanding of the migration behaviour of actinides in natural aquifer systems. The first part deals with the characterization of colloids: groundwater colloids, actinide real-colloids and actinide pseudocolloids. The second part concentrates on the generation processes and migration behaviour of actinide pseudo colloids, which are discussed with some notable experimental examples. Importance is stressed more on the chemical aspects of the actinide colloid generation in groundwater. This work is a contribution to the CEC Mirage II project, in particular the complexation and colloids research area

Colloid-colloid hydrodynamic interaction around a bend in a quasi-one-dimensional channel.

Science.gov (United States)

Liepold, Christopher; Zarcone, Ryan; Heumann, Tibor; Rice, Stuart A; Lin, Binhua

2017-07-01

We report a study of how a bend in a quasi-one-dimensional (q1D) channel containing a colloid suspension at equilibrium that exhibits single-file particle motion affects the hydrodynamic coupling between colloid particles. We observe both structural and dynamical responses as the bend angle becomes more acute. The structural response is an increasing depletion of particles in the vicinity of the bend and an increase in the nearest-neighbor separation in the pair correlation function for particles on opposite sides of the bend. The dynamical response monitored by the change in the self-diffusion [D_{11}(x)] and coupling [D_{12}(x)] terms of the pair diffusion tensor reveals that the pair separation dependence of D_{12} mimics that of the pair correlation function just as in a straight q1D channel. We show that the observed behavior is a consequence of the boundary conditions imposed on the q1D channel: both the single-file motion and the hydrodynamic flow must follow the channel around the bend.

Sampling and characterisation of groundwater colloids in ONKALO at Olkiluoto, Finland 2009-2010

International Nuclear Information System (INIS)

Jaervinen, E.; Manninen, P.; Takala, M.; Vilhunen, S.

2011-04-01

The purpose of this study was to estimate the concentration of colloids and composition of the colloid phase on the basis of the water chemistry results of filtered and unfiltered water samples and to compare the results with the previous ones. The water samples were collected from groundwater stations ONK-PVA1 in December 2009 and ONKPVA5 in June 2010. The colloid concentrations were determined from scanning electron microscopy (SEM) micrographs taken from the filters. The change in the water chemistry due to filtration was also analysed. The decrease of element concentrations due to filtration would possibly reflect the composition of the colloid phase. Because the concentration of the colloids is very low, three parallel water samples were analysed three times with an Inductively Coupled Plasma - Mass Spectrometry (ICP-MS) analyser so that the chemical differences between the filtered and unfiltered water could be evaluated. The colloid concentration in ONK-PVA1, determined by the single particle analysis of SEM micrographs, was 0.5 μg/l while the colloid concentration in ONK-PVA5 was 0.15 μg/l. The colloid phase composition could not be reliably determined due to the low colloid concentration. (orig.)

Concentration and size dependence of peak wavelength shift on quantum dots in colloidal suspension

Science.gov (United States)

Rinehart, Benjamin S.; Cao, Caroline G. L.

2016-08-01

Quantum dots (QDs) are semiconductor nanocrystals that have significant advantages over organic fluorophores, including their extremely narrow Gaussian emission bands and broad absorption bands. Thus, QDs have a wide range of potential applications, such as in quantum computing, photovoltaic cells, biological sensing, and electronics. For these applications, aliasing provides a detrimental effect on signal identification efficiency. This can be avoided through characterization of the QD fluorescence signals. Characterization of the emissivity of CdTe QDs as a function of concentration (1 to 10 mg/ml aqueous) was conducted on 12 commercially available CdTe QDs (emission peaks 550 to 730 nm). The samples were excited by a 50-mW 405-nm laser with emission collected via a free-space CCD spectrometer. All QDs showed a redshift effect as concentration increased. On average, the CdTe QDs exhibited a maximum shift of +35.6 nm at 10 mg/ml and a minimum shift of +27.24 nm at 1 mg/ml, indicating a concentration dependence for shift magnitude. The concentration-dependent redshift function can be used to predict emission response as QD concentration is changed in a complex system.

Novel star-like surfactant as dispersant for multi-walled carbon nanotubes in aqueous suspensions at high concentration

Science.gov (United States)

Qiao, Min; Ran, Qianping; Wu, Shishan

2018-03-01

A kind of novel surfactant with star-like molecular structure and terminated sulfonate was synthesized, and it was used as the dispersant for multi-walled carbon nanotubes (CNTs) in aqueous suspensions compared with a traditional single-chained surfactant. The star-like surfactant showed good dispersing ability for multi-walled CNTs in aqueous suspensions. Surface tension analysis, total organic carbon analysis, X-ray photoelectron spectroscopy, zeta potential, dynamic light scattering and transmission electron microscopy were performed to research the effect of star-like surfactant on the dispersion of multi-walled CNTs in aqueous suspensions. With the assistance of star-like surfactant, the CNTs could disperse well in aqueous suspension at high concentration of 50 g/L for more than 30 days, while the CNTs precipitated completely in aqueous suspension after 1 day without any dispersant or after 10 days with sodium 4-dodecylbenzenesulfonic acid as dispersant.

Fast microbial reduction of ferrihydrite colloids from a soil effluent

Science.gov (United States)

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

Stress modeling in colloidal dispersions undergoing non-viscometric flows

Science.gov (United States)

Dolata, Benjamin; Zia, Roseanna

2017-11-01

We present a theoretical study of the stress tensor for a colloidal dispersion undergoing non-viscometric flow. In such flows, the non-homogeneous suspension stress depends on not only the local average total stresslet-the sum of symmetric first moments of both the hydrodynamic traction and the interparticle force-but also on the average quadrupole, octupole, and higher-order moments. To compute the average moments, we formulate a six dimensional Smoluchowski equation governing the microstructural evolution of a suspension in an arbitrary fluid velocity field. Under the conditions of rheologically slow flow, where the Brownian relaxation of the particles is much faster than the spatiotemporal evolution of the flow, the Smoluchowski equation permits asymptotic solution, revealing a suspension stress that follows a second-order fluid constitutive model. We obtain a reciprocal theorem and utilize it to show that all constitutive parameters of the second-order fluid model may be obtained from two simpler linear-response problems: a suspension undergoing simple shear and a suspension undergoing isotropic expansion. The consequences of relaxing the assumption of rheologically slow flow, including the appearance of memory and microcontinuum behaviors, are discussed.

Colloid transport in dual-permeability media

Science.gov (United States)

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.

Characterization of colloids in groundwater

International Nuclear Information System (INIS)

Kim, J.I.; Buckau, G.; Klenze, R.

1987-07-01

Natural colloids in the Gorleben aquifer systems have been investigated as for their chemical composition, quantification and size distribution. Humic substances appear to be the major organic materials in these groundwaters, generating humic colloids which are analysed to be humic acid (and fulvic acid) loaded with a large number of trace heavy metal ions. These metal ions include natural homologues of actinides and some fission products in trivalent, tetravalent and hexavalent state. Concentrations of trivalent and tetravalent heavy metal ions are linearly correlated with the dissolved organic carbon (DDC) concentration in different groundwaters. The DOC is found to be present as humic colloids. The Am 3+ ions introduced in such a groundwater readily undergo the generation of its pseudocolloids through sorption or ion exchange reactions with humic colloids. The chemical behaviour of Am(III), being similar to the trivalent metal ions, e.g. Fe 3+ , REE etc. found in natural colloids, has been investigated by laser induced photoacoustic spectroscopy (LPAS). Groundwaters from Ispra, Markham Clinton and Felslabor Grimsel. Bidistilled water and one of Gorleben groundwaters, Gohy 1011, are taken for the purpose of comparison. This groundwater contains the least amount of natural colloids of all Gorleben groundwaters hitherto investigated. An indirect quantification is made by comparison of the LPAS results with experiment from Latex solution. (orig./IRB)

Development of Colloidal Gold-Based Immunochromatographic Assay for Rapid Detection of Goose Parvovirus

Directory of Open Access Journals (Sweden)

Xianglong Yu

2018-05-01

Full Text Available Goose parvovirus (GPV remains as a worldwide problem in goose industry. For this reason, it is necessary to develop a new diagnostic approach that is easier and faster than conventional tests. A rapid immunochromatographic assay based on antibody colloidal gold nanoparticles specific to GPV was developed for the detection of GPV in goose allantoic fluid and supernatant of tissue homogenate. The monoclonal antibodies (Mab was produced by immunizing the BALB/c mice with purified GPV suspension, and the polyclonal antibody (pAb was produced by immunizing the rabbits with recombinant VP3 protein. The colloidal gold was prepared by the reduction of gold salt with sodium citrate coupled with Mab against GPV. The optimal concentrations of the coating antibody and capture antibody were determined to be 1.6 mg/ml and 9 μg/ml. With visual observation, the lower limit was found to be around 1.2 μg/ml. Common diseases of goose were tested to evaluate the specificity of the immune colloidal gold (ICG strip, and no cross-reaction was observed. The clinical detection was examined by carrying out the ICG strip test with 92 samples and comparing the results of these tests with those obtained via agar diffusion test and polymerase chain reaction (PCR test. Therefore, the ICG strip test was a sufficiently sensitive and accurate detection method for a rapid screening of GPV.

Glass/Jamming Transition in Colloidal Aggregation

Science.gov (United States)

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

2000-01-01

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

Direct observation of impact propagation and absorption in dense colloidal monolayers

Science.gov (United States)

Buttinoni, Ivo; Cha, Jinwoong; Lin, Wei-Hsun; Job, Stéphane; Daraio, Chiara; Isa, Lucio

2017-11-01

Dense colloidal suspensions can propagate and absorb large mechanical stresses, including impacts and shocks. The wave transport stems from the delicate interplay between the spatial arrangement of the structural units and solvent-mediated effects. For dynamic microscopic systems, elastic deformations of the colloids are usually disregarded due to the damping imposed by the surrounding fluid. Here, we study the propagation of localized mechanical pulses in aqueous monolayers of micron-sized particles of controlled microstructure. We generate extreme localized deformation rates by exciting a target particle via pulsed-laser ablation. In crystalline monolayers, stress propagation fronts take place, where fast-moving particles (V approximately a few meters per second) are aligned along the symmetry axes of the lattice. Conversely, more viscous solvents and disordered structures lead to faster and isotropic energy absorption. Our results demonstrate the accessibility of a regime where elastic collisions also become relevant for suspensions of microscopic particles, behaving as “billiard balls” in a liquid, in analogy with regular packings of macroscopic spheres. We furthermore quantify the scattering of an impact as a function of the local structural disorder.

Sedimentation behaviour and colloidal properties of porous, chemically modified silicas in non-aqueous solvents

NARCIS (Netherlands)

Vissers, J.P.C.; Laven, J.; Claessens, H.A.; Cramers, C.A.M.G.; Agterof, W.G.M.

1997-01-01

The sedimentation behaviour and colloidal properties of porous, chemically modified silicas dispersed in non-aqueous solvents have been studied. The free settling behaviour of non-aggregated silica suspensions could effectively be described with a modified Stokes equation that takes into account the

Studies on agglomeration of colloidal suspensions in an alternating electric field; Untersuchungen zur Agglomeration kolloidaler Suspensionen im elektrischen Wechselfeld

Energy Technology Data Exchange (ETDEWEB)

Mueller, M. [Inst. fuer Mechanische Verfahrenstechnik und Mechanik, Univ. Karlsruhe (Germany); Loeffler, F. [Inst. fuer Mechanische Verfahrenstechnik und Mechanik, Univ. Karlsruhe (Germany)

1996-07-01

Colloidal solutions contain particles in the {mu}m range whose agglomeration and coagulation is of interest for certain applications. `Electrocoagulation` means that in an electric field droplets or particles in a disperse phase have higher kinetic energy so that the probability of overcoming repulsive forces and of forming bigger aggregates will increase. The electrocoagulation technique is applied for emulsion cracking of water-in-oil systems (desalination and dewatering of petroleum, petroleum cracking) and, in some cases, also for cracking oil-in-water systems. Removal of colloidal solids from aqueous solution during electrochemical waste water treatment is often carried out with the aid of dissolving aluminium or iron electrodes. The authors describe experiments in which the flow of an electric current, which would cause the electrodes to dissolve, was to be prevented. An alternating field was to induce oscillation of the particles, i.e. relative motion of the particles with respect to each other. (orig./SR) [Deutsch] Kolloidale Loesungen enthalten Partikel im {mu}m-Bereich. In manchen Bereichen ist deren Agglomeration bzw. Koagulation von Interesse. Unter dem Begriff der Elektrokoagulation versteht man im allgemeinen das Phaenomen, dass in einem elektrischen Feld Tropfen oder Partikel in einer dispersen Phase eine hoehere kinetische Energie besitzen, und dadurch die Wahrscheinlichkeit zur Ueberwindung von Abstossungskraeften und zur Bildung groesserer Aggregate steigt. Das Verfahren der Elektrokoagulation wird bisher zur Emulsionsspaltung von Wasser/Oel-Systemen (Entsaltzung und Entwaesserung von Erdoel/Erdoelspaltung) und z.T. auch zur Spaltung von Oel/Wasser-Systemen eingesetzt. Zur Entfernung kolloidaler Feststoffe aus waessrigen Loesungen bei der elektrochemischen Aufarbeitung von Abwasser wird haeufig mit sich aufloesenden Aluminium- oder Eisenelektroden gearbeitet. In den im folgenden dargestellten Untersuchungen sollte ein Stromfluss durch die

Far-from-equilibrium sheared colloidal liquids: Disentangling relaxation, advection, and shear-induced diffusion

KAUST Repository

Lin, Neil Y. C.

2013-12-01

Using high-speed confocal microscopy, we measure the particle positions in a colloidal suspension under large-amplitude oscillatory shear. Using the particle positions, we quantify the in situ anisotropy of the pair-correlation function, a measure of the Brownian stress. From these data we find two distinct types of responses as the system crosses over from equilibrium to far-from-equilibrium states. The first is a nonlinear amplitude saturation that arises from shear-induced advection, while the second is a linear frequency saturation due to competition between suspension relaxation and shear rate. In spite of their different underlying mechanisms, we show that all the data can be scaled onto a master curve that spans the equilibrium and far-from-equilibrium regimes, linking small-amplitude oscillatory to continuous shear. This observation illustrates a colloidal analog of the Cox-Merz rule and its microscopic underpinning. Brownian dynamics simulations show that interparticle interactions are sufficient for generating both experimentally observed saturations. © 2013 American Physical Society.

Assembly of vorticity-aligned hard-sphere colloidal strings in a simple shear flow

KAUST Repository

Cheng, X.

2011-12-23

Colloidal suspensions self-assemble into equilibrium structures ranging from face- and body-centered cubic crystals to binary ionic crystals, and even kagome lattices. When driven out of equilibrium by hydrodynamic interactions, even more diverse structures can be accessed. However, mechanisms underlying out-of-equilibrium assembly are much less understood, though such processes are clearly relevant in many natural and industrial systems. Even in the simple case of hard-sphere colloidal particles under shear, there are conflicting predictions about whether particles link up into string-like structures along the shear flow direction. Here, using confocal microscopy, we measure the shear-induced suspension structure. Surprisingly, rather than flow-aligned strings, we observe log-rolling strings of particles normal to the plane of shear. By employing Stokesian dynamics simulations, we address the mechanism leading to this out-of-equilibrium structure and show that it emerges from a delicate balance between hydrodynamic and interparticle interactions. These results demonstrate a method for assembling large-scale particle structures using shear flows.

Far-from-equilibrium sheared colloidal liquids: Disentangling relaxation, advection, and shear-induced diffusion

KAUST Repository

Lin, Neil Y. C.; Goyal, Sushmit; Cheng, Xiang; Zia, Roseanna N.; Escobedo, Fernando A.; Cohen, Itai

2013-01-01

Using high-speed confocal microscopy, we measure the particle positions in a colloidal suspension under large-amplitude oscillatory shear. Using the particle positions, we quantify the in situ anisotropy of the pair-correlation function, a measure of the Brownian stress. From these data we find two distinct types of responses as the system crosses over from equilibrium to far-from-equilibrium states. The first is a nonlinear amplitude saturation that arises from shear-induced advection, while the second is a linear frequency saturation due to competition between suspension relaxation and shear rate. In spite of their different underlying mechanisms, we show that all the data can be scaled onto a master curve that spans the equilibrium and far-from-equilibrium regimes, linking small-amplitude oscillatory to continuous shear. This observation illustrates a colloidal analog of the Cox-Merz rule and its microscopic underpinning. Brownian dynamics simulations show that interparticle interactions are sufficient for generating both experimentally observed saturations. © 2013 American Physical Society.

Sampling and characterisation of groundwater colloids in ONKALO at Olkiluoto, Finland in 2007

International Nuclear Information System (INIS)

Takala, M.; Manninen, P.

2008-08-01

Colloid samples were collected from ONKALO groundwater station ONK-PVA1 in October 2007 and an additional sample was taken from groundwater station ONK-PVA3 in November 2007. The colloids were collected by filtering the groundwater on site with an Anopore 0.02 μm aluminium oxide filter. In the sampling in October, water samples were also collected to analyse the differences in the water chemistry before and after filtration. The water samples were freeze-dried so that the elements would be concentrated in the water. The colloid concentrations were determined by counting the particles from the SEM micrographs and by calculating the concentration using the micrograph area, the filter area and the filtered volume. The colloid concentration in ONK-PVA1 was very low. The particle concentration within the size range from 0.1 μm to 1 μm was 1.6 x 10 4 pt/L and the mass concentration within the same size range 0.001 μg/L. Owing to the very low concentration, an additional colloid sample was taken from ONK-PVA3. The colloid concentration in ONK-PVA3 within the size range from 0.1 μm to 1 μm was 8.2 x 10 7 pt/L and the mass concentration 0.013 mg/L. When studying the ONKALO groundwater monitoring data it was noticed that in the samples where the colloid concentration was elevated also the sodium fluorescein concentration was probably elevated. This indicated that process water (e.g. drilling water) was present in the water samples. The ONK-PVA1 water probably also contained process water during the colloid sampling performed in 2006. The composition of the colloid phase could not be determined by analysing the differences in the filtered and unfiltered water owing to the low colloid concentration. Furthermore, the aluminium oxide filter caused aluminium contamination. (orig.)

Formation and transport of radioactive colloids in porous media

International Nuclear Information System (INIS)

Chung, J.Y.; Lee, K.J.

1993-01-01

This paper deals with the effect of the presence of colloids in natural groundwater on radionuclide transport. The system considered here treats groundwater as a dispersing medium and colloid or finely divided solid material resulting from several different repository sources as a dispersed phase. Evaluation of the radionuclides adsorption on colloid, concepts of effective transport velocity and migration distance, and mathematical formulation of the filtration equation were driven, along with the case studies using typical parameter values of a conceptual radioactive waste repository and concentration on the effect of poly dispersed colloid on radionuclide transport. This paper also introduces the three phase analysis to treat the radionuclide transport more practically. When compared with the previously published experimental data, the modified filtration equation gives a satisfactory result. Results of the case studies show that the reduction of colloidal size enhances the corresponding colloid concentration when colloidal transport is only affected by diffusion phenomena. However, the three phase analysis shows that this trend can be reversed if the colloidal filtration becomes a dominant mechanism in the colloidal transport. Consequently, these results show that colloid could play a very important role in radionuclide transport under a repository environment

EOS9nT: A TOUGH2 module for the simulation of flow and solute/colloid transport

International Nuclear Information System (INIS)

Moridis, G.J.; Wu, Y.S.; Pruess, K.

1998-04-01

EOS9nT is a new TOUGH2 module for the simulation of flow and transport of an arbitrary number n of tracers (solutes and/or colloids) in the subsurface. The module first solves the flow-related equations, which are comprised of (a) the Richards equation and, depending on conditions, may also include (b) the flow equation of a dense brine or aqueous suspension and/or (c) the heat equation. A second set of transport equations, corresponding to the n tracers, are then solved sequentially. The low concentrations of the n tracers are considered to have no effect on the liquid phase, thus making possible the decoupling of their equations. The first set of equations in EOS9nT provides the flow regime and account for fluid density variations due to thermal and/or solute concentration effects. The n tracer transport equations account for sorption, radioactive decay, advection, hydrodynamic dispersion, molecular diffusion, as well as filtration (for colloids only). EOS9nT can handle gridblocks or irregular geometry in three-dimensional domains. Preliminary results from four 1-D verification problems show an excellent agreement between the numerical predictions and the known analytical solutions

Studies of colloids and their importance for repository performance assessment

International Nuclear Information System (INIS)

Laaksoharju, M.; Skaarman, C.; Degueldre, C.

1995-12-01

The processes, parameters and data used to evaluate the potential of nuclide transport by a colloid facilitated mechanism are reviewed and discussed in this report. Both steady-state (present situation) and possible future non-steady-state hydrogeochemistry in the geosphere are covered. In the steady-state scenario, the colloid (clay, silica, iron(III)hydroxide) concentration is around 20-45 micrograms/l which is considered to be a low value. The low colloid concentration is justified by the large attachment factor to the rock which reduces the stability of the colloids in the aquifer. Both reversible and irreversible sorption processes are reviewed. In the non-steady-state scenario, changes of hydrogeochemical properties may induce larger colloid concentrations. The increase of concentration is however limited and relaxation is always observed after any change. Emphasis is placed on the glaciation-deglaciation scenario. 53 refs, 12 figs, 3 tabs

Composition inversion in mixtures of binary colloids and polymer

Science.gov (United States)

Zhang, Isla; Pinchaipat, Rattachai; Wilding, Nigel B.; Faers, Malcolm A.; Bartlett, Paul; Evans, Robert; Royall, C. Patrick

2018-05-01

Understanding the phase behaviour of mixtures continues to pose challenges, even for systems that might be considered "simple." Here, we consider a very simple mixture of two colloidal and one non-adsorbing polymer species, which can be simplified even further to a size-asymmetrical binary mixture, in which the effective colloid-colloid interactions depend on the polymer concentration. We show that this basic system exhibits surprisingly rich phase behaviour. In particular, we enquire whether such a system features only a liquid-vapor phase separation (as in one-component colloid-polymer mixtures) or whether, additionally, liquid-liquid demixing of two colloidal phases can occur. Particle-resolved experiments show demixing-like behaviour, but when combined with bespoke Monte Carlo simulations, this proves illusory, and we reveal that only a single liquid-vapor transition occurs. Progressive migration of the small particles to the liquid phase as the polymer concentration increases gives rise to composition inversion—a maximum in the large particle concentration in the liquid phase. Close to criticality, the density fluctuations are found to be dominated by the larger colloids.

Decrease of concentration and colloidal fraction of organic carbon and trace elements in response to the anomalously hot summer 2010 in a humic boreal lake

International Nuclear Information System (INIS)

Shirokova, L.S.; Pokrovsky, O.S.; Moreva, O.Yu.; Chupakov, A.V.; Zabelina, S.A.; Klimov, S.I.; Shorina, N.V.; Vorobieva, T.Ya.

2013-01-01

The colloidal distribution and size fractionation of organic carbon (OC), major elements and trace elements (TE) were studied in a seasonally stratified, organic-rich boreal lake, Lake Svyatoe, located in the European subarctic zone (NW Russia, Arkhangelsk region). This study took place over the course of 4 years in both winter and summer periods using an in situ dialysis technique (1 kDa, 10 kDa and 50 kDa) and traditional frontal filtration and ultrafiltration (5, 0.22 and 0.025 μm). We observed a systematic difference in dissolved elements and colloidal fractions between summer and winter periods with the highest proportion of organic and organo-ferric colloids (1 kDa–0.22 μm) observed during winter periods. The anomalously hot summer of 2010 in European Russia produced surface water temperatures of approximately 30 °C, which were 10° above the usual summer temperatures and brought about crucial changes in element speciation and size fractionation. In August 2010, the concentration of dissolved organic carbon (DOC) decreased by more than 30% compared to normal period, while the relative proportion of organic colloids decreased from 70–80% to only 20–30% over the full depth of the water column. Similarly, the proportion of colloidal Fe decreased from 90–98% in most summers and winters to approximately 60–70% in August 2010. During this hot summer, measurable and significant (> 30% compared to other periods) decreases in the colloidal fractions of Ca, Mg, Sr, Ba, Al, Ti, Ni, As, V, Co, Y, all rare earth elements (REEs), Zr, Hf, Th and U were also observed. In addition, dissolved ( 100 for Co), the second and third factors could have brought about the decrease of allochthonous DOC concentration as well as the concentration and proportion of organic and organo-mineral colloidal forms of non-essential low-soluble trace elements present in the form of organic colloids (Al, Y, Ti, Zr, Hf, Th, Pb, all REEs). It can be hypothesized that climate warming in

Formation mechanisms of colloidal silica via sodium silicate

International Nuclear Information System (INIS)

Tsai, M.-S.; Huang, P.Y.; Yang, C.-H.

2006-01-01

Colloidal silica is formed by titrating active silicic acid into a heated KOH with seed solution. The colloidal silica formation mechanisms are investigated by sampling the heated solution during titration. In the initial stage, the added seeds were dissolved. This might due to the dilution of seed concentration, the addition of potassium hydroxide (KOH) and the heating at 100 deg. C. Homogenous nucleation and surface growth occur simultaneously in the second stage of colloidal silica formation. Homogenous nucleation is more important when the seed concentration is relatively low. On the other hand, surface growth plays an important role when the seed concentration is increased. In the middle seed concentration, the seed particles grow up and some new small particles are born by the homogenous nucleation process to form a bimodal size distribution product. As the titrating volume of active silicic acid exceeds a specific value in the last stage the particle size increases rapidly and the particle number decreases, which may be caused by the aggregation of particles. The intervals between each stage were varied with the seed concentration. Increasing the seed concentration led to the formation of uniform particle size colloidal silica

Colloid remediation in groundwater by polyelectrolyte capture

International Nuclear Information System (INIS)

Nuttall, H.E.; Rao, S.; Jain, R.

1992-01-01

This paper describes an ongoing study to characterize groundwater colloids, to understand the geochemical factors affecting colloid transport in groundwater, and to develop an in-situ colloid remediation process. The colloids and suspended particulate matter used in this study were collected from a perched aquifer site that has radiation levels several hundred times the natural background and where previous researchers have measured and reported the presence of radiocolloids containing plutonium and americium. At this site, radionuclides have spread over several kilometers. Inorganic colloids collected from water samples are characterized with respect to concentration, mineralogy, size distribution, electrophoretic mobility (zeta potential), and radioactivity levels. Presented are the methods used to investigate the physiochemical factors affecting colloid transport and the preliminary analytical results. Included below are a description of a colloid transport model and the corresponding computational code, water analyses, characterization of the inorganic colloids, and a conceptual description of a process for in-situ colloid remediation using the phenomenon of polyelectrolyte capture

The role of colloids in the transport of radionuclides in geological media

International Nuclear Information System (INIS)

Moulin, V.

1993-01-01

The main objective of this programme is to understand how colloids could influence the migration behaviour of radionuclides in geological formations. This is being achieved firstly, by identifying the retention mechanisms of colloids and pseudocolloids (association of radionuclides with colloids) on mineral surfaces by static and dynamic experiments, and secondly by investigating the formation of pseudocolloids. Moreover, these studies will be focused on model systems (surfaces, colloids) selected from studies carried out on the El Berrocal site (characterization of the granite, of the colloids). Two types of experiments are planned: for the study of pseudocolloid formation, sorption experiments (batch tests) with radionuclides will be conducted either with model inorganic colloidal suspensions or with mineral monoliths as macroscopic surfaces of colloids. Dynamic experiments will be performed using well-defined packings of both synthetic and natural minerals (major constituents of granite). Moreover, a particular attention will be devoted to the organic coatings (in static and dynamic conditions). These studies will provide data directly usable by migration models to predict colloid transport under conditions relevant to geological disposals. This programme will be carried out in collaboration with the different partners of this contract: CEA (Fontenay-aux-Roses/F), CIEMAT (Madrid/S), CNRS (Orsay/F), GERMETRAD (Nantes/F), GSF (Munich/G), INFM (Padua/I), INTERA (London/UK) with Dr V. Moulin, Dr P. Rivas, Dr J.C. Dran, Pr Pieri, Dr C. Wolfrum, Pr G. Della Mea and Dr P. Grindrod as project leaders respectively. 4 refs., 2 figs., 1 tab

Experimental analysis of colloid capture by a cylindrical collector in laminar overland flow.

Science.gov (United States)

Wu, Lei; Gao, Bin; Muñoz-Carpena, Rafael

2011-09-15

Although colloid-facilitated contaminant transport in water flow is a well-known contamination process, little research has been conducted to investigate the transport of colloidal particles through emergent vegetation in overland flow. In this work, a series of laboratory experiments were conducted to measure the single-collector contact efficiency (η(0)) of colloid capture by a simulated plant stem in laminar lateral flow. Fluorescent microspheres of various sizes were used as experimental colloids. The colloid suspensions were applied to a glass cylinder installed in a small size flow chamber at different flow rates. Two cylinder sizes were tested in the experiment and silicone grease was applied to the cylinder surface to make it favorable for colloid deposition. Our results showed that increases in flow rate and collector size reduced the value of η(0) and a minimum value of η(0) might exist for a colloid size. The experimental data were compared to theoretical predictions of different single-collector contact efficiency models. The results indicated that existing single-collector contact efficiency models underestimated the η(0) of colloid capture by the cylinders in laminar overland flow. A regression equation of η(0) as a function of collector Reynolds number (Re(c)) and Peclet number (N(Pe)) was developed and fit the experimental data very well (R(2) > 0.98). This regression equation can be used to help construct and refine mathematical models of colloid transport and filtration in laminar overland flow on vegetated surfaces.

Chancellor Water Colloids: Characterization and Radionuclide Associated Transport

Energy Technology Data Exchange (ETDEWEB)

Reimus, Paul William [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Boukhalfa, Hakim [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2014-09-26

Column transport experiments were conducted in which water from the Chancellor nuclear test cavity was transported through crushed volcanic tuff from Pahute Mesa. In one experiment, the cavity water was spiked with solute ¹³⁷Cs, and in another it was spiked with ^239/240Pu(IV) nanocolloids. A third column experiment was conducted with no radionuclide spike at all, although the ¹³⁷Cs concentrations in the water were still high enough to quantify in the column effluent. The radionuclides strongly partitioned to natural colloids present in the water, which were characterized for size distribution, mass concentration, zeta potential/surface charge, critical coagulation concentration, and qualitative mineralogy. In the spiked water experiments, the unanalyzed portion of the high-concentration column effluent samples were combined and re-injected into the respective columns as a second pulse. This procedure was repeated again for a third injection. Measurable filtration of the colloids was observed after each initial injection of the Chancellor water into the columns, but the subsequent injections (spiked water experiments only) exhibited no apparent filtration, suggesting that the colloids that remained mobile after relatively short transport distances were more resistant to filtration than the initial population of colloids. It was also observed that while significant desorption of ¹³⁷Cs from the colloids occurred after the first injection in both the spiked and unspiked waters, subsequent injections of the spiked water exhibited much less ¹³⁷Cs desorption (much greater ¹³⁷Cs colloid-associated transport). This result suggests that the ¹³⁷Cs that remained associated with colloids during the first injection represented a fraction that was more strongly adsorbed to the mobile colloids than the initial ¹³⁷Cs associated with the colloids. A greater amount of the ^239/240

Colloidal stability of suspended and agglomerate structures of settled carbon nanotubes in different aqueous matrices.

Science.gov (United States)

Schwyzer, Irène; Kaegi, Ralf; Sigg, Laura; Nowack, Bernd

2013-08-01

Carbon nanotubes (CNTs) are often processed in suspended form and therefore a release of CNT-suspensions into the aquatic environment is plausible. In this study, the behaviour of two physico-chemically very different CNT types in the presence of varying, environmentally relevant calcium-containing media was investigated, including the long-term colloidal stability and the sedimentary structures of settled CNTs. Calcium induced CNT flocculation, however, the stability of the CNTs in the medium did not monotonously decrease with increasing calcium concentration. At intermediate calcium concentrations (0.5-1.5 mM Ca) pre-dispersed CNTs were stabilized in humic acid medium to similar, temporarily even to higher degree than in the absence of calcium. Between pH 5 and 8 only at the highest pH an influence on CNT stability was observed by either promoting flocculation or stabilisation depending on the CNT type. Humic acid stabilized CNTs much better than fulvic acid. Generally, the colloidal stability of the long, thick CNTs with higher surface oxygen content was less affected by the media composition. An investigation of the settled CNT material using analytical electron microscopy revealed the presence of spheroidal, bundle-like and net like CNT-agglomerate structures. Calcium possibly acted as bridging agent linking CNTs in a network like manner, temporarily increasing the CNT concentrations stabilized in the supernatants due to the low density of these structures. With increasing settling time the CNTs formed a fluffy sediment layer at the bottom of the reaction vessels. Bundle-like CNT agglomerates were also observed within that layer of settled CNTs, possibly caused by calcium neutralizing the surface charges. Furthermore, the CNT suspensions contained spheroidal CNT agglomerates, most likely residues from the original dry powder that were not disaggregated. The analysis of settled CNT material is a novelty and illustrates CNT agglomerate structures possibly

Transport of Intrinsic Plutonium Colloids in Saturated Porous Media

Science.gov (United States)

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

Micro-rheology on (polymer-grafted) colloids using optical tweezers

International Nuclear Information System (INIS)

Gutsche, C; Elmahdy, M M; Kegler, K; Semenov, I; Stangner, T; Otto, O; Ueberschaer, O; Kremer, F; Keyser, U F; Krueger, M; Rauscher, M; Weeber, R; Harting, J; Kim, Y W; Lobaskin, V; Netz, R R

2011-01-01

Optical tweezers are experimental tools with extraordinary resolution in positioning (± 1 nm) a micron-sized colloid and in the measurement of forces (± 50 fN) acting on it-without any mechanical contact. This enables one to carry out a multitude of novel experiments in nano- and microfluidics, of which the following will be presented in this review: (i) forces within single pairs of colloids in media of varying concentration and valency of the surrounding ionic solution, (ii) measurements of the electrophoretic mobility of single colloids in different solvents (concentration, valency of the ionic solution and pH), (iii) similar experiments as in (i) with DNA-grafted colloids, (iv) the nonlinear response of single DNA-grafted colloids in shear flow and (v) the drag force on single colloids pulled through a polymer solution. The experiments will be described in detail and their analysis discussed.

Experimental analysis of an effect of the nutrient type and its concentration on the rheological properties of the baker’s yeast suspensions

Directory of Open Access Journals (Sweden)

Major-Godlewska Marta

2015-09-01

Full Text Available The aim of the study presented was to experimentally analyze an effect of the nutrient type and its concentration on the variability of rheological properties of the baker’s yeast suspensions for different time periods. Aqueous suspensions of the baker’s yeast of various concentration (solution I, without nutrient and yeasts suspended in aqueous solution of sucrose or honey as nutrients with different concentration (solution II or solution III were tested. Experiments were carried out using rotational rheoviscometer of type RT10 by a company HAAKE. The measurements were conducted for different time periods (from 1 h up to 144 h at given fluid temperature. On the basis of the obtained data, rheological characteristics of the aqueous solution of baker’s yeast suspensions without and with nutrients of different sucrose or honey concentration were identified and mathematically described.

Elaboration of hybrid materials by templating with mineral liquid crystals stabilization of a mixed sol of YSZ nanoparticles and V2O5 ribbon-like colloids

International Nuclear Information System (INIS)

Guiot, C.

2009-01-01

The purpose of this PhD was to investigate innovative soft chemistry ways to prepare hybrid materials with ordered nano-structures. Concretely, research were conducted on the development of a hybrid material made of an yttria-stabilized zirconia (YSZ) matrix templated by a mineral liquid crystal, namely V 2 O 5 . In aqueous solutions, vanadium oxide exhibits ribbon-like colloids of typical dimensions 1 nm x 25 nm x 500 nm, stabilized by a strong negative surface charge. Above a critical concentration, the anisotropic colloids assemble into a nematic liquid crystal, whose domains can be oriented within the same direction over a macroscopic range under a weak magnetic field. The idea is to use V 2 O 5 anisotropic colloids as a template for a hybrid material, taking advantage of their ordering behavior. Preliminary experiments revealed a strong reactivity between molecular compounds of zirconium and vanadium oxide. Therefore, the studies were directed toward the preparation of a mixed colloidal sol containing YSZ nanoparticles and vanadium oxide ribbon-like colloids, as a precursor sol for the intended hybrid material. The YSZ nanoparticles are obtained through an outstanding hydrothermal synthesis leading to a stable suspension of nanocrystalline particles of ca. 5 nm, in pure water. Providing a mixed sol of YSZ and V 2 O 5 is a key challenge for it implies the co-stabilization of two types of colloids having different shape, size and surface properties. Besides, the existence of V 2 O 5 in its ribbon-like form requires acidic conditions and very low ionic strength. The first part of this work was then dedicated to the study of electro-steric stabilization of zirconia suspension by addition of acidic poly-electrolytes. Different polymers with carboxylic and/or sulfonic acidic functions were investigated. Based on zeta potential measurements and adsorption isotherms, the influence of molecular weight and polymer charge were discussed. Among the studied polymers, poly

Saturated Zone Colloid Transport

International Nuclear Information System (INIS)

H. S. Viswanathan

2004-01-01

sorbed onto this fraction of colloids also transport without retardation. The transport times for these radionuclides will be the same as those for nonsorbing radionuclides. The fraction of nonretarding colloids developed in this analysis report is used in the abstraction of SZ and UZ transport models in support of the total system performance assessment (TSPA) for the license application (LA). This analysis report uses input from two Yucca Mountain Project (YMP) analysis reports. This analysis uses the assumption from ''Waste Form and In-Drift Colloids-Associated Radionuclide Concentrations: Abstraction and Summary'' that plutonium and americium are irreversibly sorbed to colloids generated by the waste degradation processes (BSC 2004 [DIRS 170025]). In addition, interpretations from RELAP analyses from ''Saturated Zone In-Situ Testing'' (BSC 2004 [DIRS 170010]) are used to develop the retardation factor distributions in this analysis

Morphological instability of a non-equilibrium ice-colloid interface

KAUST Repository

Peppin, S. S. L.

2009-10-02

We assess the morphological stability of a non-equilibrium ice-colloidal suspension interface, and apply the theory to bentonite clay. An experimentally convenient scaling is employed that takes advantage of the vanishing segregation coefficient at low freezing velocities, and when anisotropic kinetic effects are included, the interface is shown to be unstable to travelling waves. The potential for travelling-wave modes reveals a possible mechanism for the polygonal and spiral ice lenses observed in frozen clays. A weakly nonlinear analysis yields a long-wave evolution equation for the interface shape containing a new parameter related to the highly nonlinear liquidus curve in colloidal systems. We discuss the implications of these results for the frost susceptibility of soils and the fabrication of microtailored porous materials. © 2009 The Royal Society.

Decrease of concentration and colloidal fraction of organic carbon and trace elements in response to the anomalously hot summer 2010 in a humic boreal lake.

Science.gov (United States)

Shirokova, L S; Pokrovsky, O S; Moreva, O Yu; Chupakov, A V; Zabelina, S A; Klimov, S I; Shorina, N V; Vorobieva, T Ya

2013-10-01

The colloidal distribution and size fractionation of organic carbon (OC), major elements and trace elements (TE) were studied in a seasonally stratified, organic-rich boreal lake, Lake Svyatoe, located in the European subarctic zone (NW Russia, Arkhangelsk region). This study took place over the course of 4 years in both winter and summer periods using an in situ dialysis technique (1 kDa, 10 kDa and 50 kDa) and traditional frontal filtration and ultrafiltration (5, 0.22 and 0.025 μm). We observed a systematic difference in dissolved elements and colloidal fractions between summer and winter periods with the highest proportion of organic and organo-ferric colloids (1 kDa-0.22 μm) observed during winter periods. The anomalously hot summer of 2010 in European Russia produced surface water temperatures of approximately 30°C, which were 10° above the usual summer temperatures and brought about crucial changes in element speciation and size fractionation. In August 2010, the concentration of dissolved organic carbon (DOC) decreased by more than 30% compared to normal period, while the relative proportion of organic colloids decreased from 70-80% to only 20-30% over the full depth of the water column. Similarly, the proportion of colloidal Fe decreased from 90-98% in most summers and winters to approximately 60-70% in August 2010. During this hot summer, measurable and significant (>30% compared to other periods) decreases in the colloidal fractions of Ca, Mg, Sr, Ba, Al, Ti, Ni, As, V, Co, Y, all rare earth elements (REEs), Zr, Hf, Th and U were also observed. In addition, dissolved (organic matter by heterotrophic aerobic bacterioplankton and 3) photo-degradation of DOM and photo-chemical liberation of organic-bound TE. While the first process may have caused significant decreases in the total dissolved concentration of micronutrients (a factor of 2 to 5 for Cr, Mn, Fe, Ni, Cu, Zn and Cd and a factor of >100 for Co), the second and third factors could have brought

Colloidal silver: a novel treatment for Staphylococcus aureus biofilms?

Science.gov (United States)

Goggin, Rachel; Jardeleza, Camille; Wormald, Peter-John; Vreugde, Sarah

2014-03-01

Colloidal silver is an alternative medicine consisting of silver particles suspended in water. After using this solution as a nasal spray, the symptoms of a previously recalcitrant Staphylococcus aureus (S. aureus)-infected chronic rhinosinusitis patient were observed to have improved markedly. The aim of this study was to determine whether colloidal silver has any direct bactericidal effects on these biofilms in vitro. S. aureus biofilms were grown from the ATCC 25923 reference strain on Minimum Biofilm Eradication Concentration (MBEC) device pegs, and treated with colloidal silver. Concentrations tested ranged from 10 to 150 μL colloidal silver diluted to 200 μL with sterile water in 50 μL cerebrospinal fluid (CSF) broth. Control pegs were exposed to equivalent volumes of CSF broth and sterile water. The sample size was 4 biomass values per treatment or control group. Confocal scanning laser microscopy and COMSTAT software were used to quantify biofilms 24 hours after treatment. Significant differences from control were found for all concentrations tested bar the lowest of 10 μL colloidal silver in 200 μL. At 20 μL colloidal silver, the reduction in biomass was 98.9% (mean difference between control and treatment = -4.0317 μm(3) /μm(2) , p colloidal silver (mean differences = -4.0681 and -4.0675μm(3) /μm(2) , respectively, p Colloidal silver directly attenuates in vitro S. aureus biofilms. © 2014 ARS-AAOA, LLC.

Characterization of colloids found in various groundwater environments in central and southern Nevada

International Nuclear Information System (INIS)

Kingston, W.L.; Whitbeck, M.

1991-07-01

Colloid concentration and composition were determined and compared for 23 groundwater samples collected in central and southern Nevada. Mean colloid concentration in the 1.0 to 0.03 μm range is 0.9 mg/l. Composition consists of silica (cristobalite, fused silica, or amorphous silica) and possibly small amounts of clay or zeolite. Calcite and organic material were also identified, but may be sampling artifacts or contaminants. Concentrations of colloidal-sized particles are similar for the following sample groups: (1) carbonate and volcanic; (2) well and spring; and (3) Nevada Test Site (NTS) and off-NTS sites. Trends were not observed between water chemistry and either colloid concentration or composition. Absorption studies performed in the laboratory indicate that cesium-137, cobalt-60, and europium-152 adsorb to colloids collected from the NTS. Comparisons of colloid and rock distribution coefficient (K d s) suggest that europium will preferentially absorb to these colloids compared to tuffaceous rocks of the NTS

Self-Suspended Suspensions of Covalently Grafted Hairy Nanoparticles

KAUST Repository

Choudhury, Snehashis

2015-03-17

© 2015 American Chemical Society. Dispersions of small particles in liquids have been studied continuously for almost two centuries for their ability to simultaneously advance understanding of physical properties of fluids and their widespread use in applications. In both settings, the suspending (liquid) and suspended (solid) phases are normally distinct and uncoupled on long length and time scales. In this study, we report on the synthesis and physical properties of a novel family of covalently grafted nanoparticles that exist as self-suspended suspensions with high particle loadings. In such suspensions, we find that the grafted polymer chains exhibit unusual multiscale structural transitions and enhanced conformational stability on subnanometer and nanometer length scales. On mesoscopic length scales, the suspensions display exceptional homogeneity and colloidal stability. We attribute this feature to steric repulsions between grafted chains and the space-filling constraint on the tethered chains in the single-component self-suspended materials, which inhibits phase segregation. On macroscopic length scales, the suspensions exist as neat fluids that exhibit soft glassy rheology and, counterintuitively, enhanced elasticity with increasing temperature. This feature is discussed in terms of increased interpenetration of the grafted chains and jamming of the nanoparticles. (Chemical Presented).

Single-particle colloid tracking in four dimensions.

Science.gov (United States)

Anthony, Stephen M; Hong, Liang; Kim, Minsu; Granick, Steve

2006-11-21

Coating a close-packed fluorescent colloid monolayer with a nanometer-thick metal film followed by sonication in liquid produces modulated optical nanoprobes. The metal coating modulates the fluorescence as these structures rotate in suspension, enabling the use of these particles as probes to monitor both rotational and center-of-mass (translational) dynamics in complex environments. Here, we demonstrate methods to simultaneously measure two translational and two rotational degrees of freedom, with excellent agreement to theory. The capability to determine two angles of rotation opens several new avenues of future research.

Detection of colloidal silver chloride near solubility limit

Science.gov (United States)

Putri, K. Y.; Adawiah, R.

2018-03-01

Detection of nanoparticles in solution has been made possible by several means; one of them is laser-induced breakdown detection (LIBD). LIBD is able to distinguish colloids of various sizes and concentrations. This technique has been used in several solubility studies. In this study, the formation of colloids in a mixed system of silver nitrate and sodium chloride was observed by acoustic LIBD. Silver chloride has low solubility limit, therefore LIBD measurement is appropriate. Silver and chloride solutions with equal concentrations, set at below and above the solubility of silver chloride as the expected solid product, were mixed and the resulting colloids were observed. The result of LIBD measurement showed that larger particles were present as more silver and chloride introduced. However, once the concentrations exceeded the solubility limit of silver chloride, the detected particle size seemed to be decreasing, hence suggested the occurrence of coprecipitation process. This phenomenon indicated that the ability of LIBD to detect even small changes in colloid amounts might be a useful tool in study on formation and stability of colloids, i.e. to confirm whether nanoparticles synthesis has been successfully performed and whether the system is stable or not.

Polymorphism in Bacterial Flagella Suspensions

Science.gov (United States)

Schwenger, Walter J.

Bacterial flagella are a type of biological polymer studied for its role in bacterial motility and the polymorphic transitions undertaken to facilitate the run and tumble behavior. The naturally rigid, helical shape of flagella gives rise to novel colloidal dynamics and material properties. This thesis studies methods in which the shape of bacterial flagella can be controlled using in vitro methods and the changes the shape of the flagella have on both single particle dynamics and bulk material properties. We observe individual flagellum in both the dilute and semidilute regimes to observe the effects of solvent condition on the shape of the filament as well as the effect the filament morphology has on reptation through a network of flagella. In addition, we present rheological measurements showing how the shape of filaments effects the bulk material properties of flagellar suspensions. We find that the individual particle dynamics in suspensions of flagella can vary with geometry from needing to reptate linearly via rotation for helical filaments to the prevention of long range diffusion for block copolymer filaments. Similarly, for bulk material properties of flagella suspensions, helical geometries show a dramatic enhancement in elasticity over straight filaments while block copolymers form an elastic gel without the aid of crosslinking agents.

Size-dependent optical properties of colloidal PbS quantum dots.

Science.gov (United States)

Moreels, Iwan; Lambert, Karel; Smeets, Dries; De Muynck, David; Nollet, Tom; Martins, José C; Vanhaecke, Frank; Vantomme, André; Delerue, Christophe; Allan, Guy; Hens, Zeger

2009-10-27

We quantitatively investigate the size-dependent optical properties of colloidal PbS nanocrystals or quantum dots (Qdots), by combining the Qdot absorbance spectra with detailed elemental analysis of the Qdot suspensions. At high energies, the molar extinction coefficient epsilon increases with the Qdot volume d(3) and agrees with theoretical calculations using the Maxwell-Garnett effective medium theory and bulk values for the Qdot dielectric function. This demonstrates that quantum confinement has no influence on epsilon in this spectral range, and it provides an accurate method to calculate the Qdot concentration. Around the band gap, epsilon only increases with d(1.3), and values are comparable to the epsilon of PbSe Qdots. The data are related to the oscillator strength f(if) of the band gap transition and results agree well with theoretical tight-binding calculations, predicting a linear dependence of f(if) on d. For both PbS and PbSe Qdots, the exciton lifetime tau is calculated from f(if). We find values ranging between 1 and 3 mus, in agreement with experimental literature data from time-resolved luminescence spectroscopy. Our results provide a thorough general framework to calculate and understand the optical properties of suspended colloidal quantum dots. Most importantly, it highlights the significance of the local field factor in these systems.

Oppositely charged colloids out of equilibrium

Science.gov (United States)

Vissers, T.

2010-11-01

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

Saturated Zone Colloid Transport

Energy Technology Data Exchange (ETDEWEB)

H. S. Viswanathan

2004-10-07

retardation. Radionuclides irreversibly sorbed onto this fraction of colloids also transport without retardation. The transport times for these radionuclides will be the same as those for nonsorbing radionuclides. The fraction of nonretarding colloids developed in this analysis report is used in the abstraction of SZ and UZ transport models in support of the total system performance assessment (TSPA) for the license application (LA). This analysis report uses input from two Yucca Mountain Project (YMP) analysis reports. This analysis uses the assumption from ''Waste Form and In-Drift Colloids-Associated Radionuclide Concentrations: Abstraction and Summary'' that plutonium and americium are irreversibly sorbed to colloids generated by the waste degradation processes (BSC 2004 [DIRS 170025]). In addition, interpretations from RELAP analyses from ''Saturated Zone In-Situ Testing'' (BSC 2004 [DIRS 170010]) are used to develop the retardation factor distributions in this analysis.

Electroacoustic theory for concentrated colloids with overlapped DLs at arbitrary kappa alpha. I. Application to nanocolloids and nonaqueous colloids.

Science.gov (United States)

Shilov, V N; Borkovskaja, Y B; Dukhin, A S

2004-09-15

Existing theories of electroacoustic phenomena in concentrated colloids neglect the possibility of double layer overlap and are valid mostly for the "thin double layer," when the double layer thickness is much less than the particle size. In this paper we present a new electroacoustic theory which removes this restriction. This would make this new theory applicable to characterizing a variety of aqueous nanocolloids and of nonaqueous dispersions. There are two versions of the theory leading to the analytical solutions. The first version corresponds to strongly overlapped diffuse layers (so-called quasi-homogeneous model). It yields a simple analytical formula for colloid vibration current (CVI), which is valid for arbitrary ultrasound frequency, but for restricted kappa alpha range. This version of the theory, as well the Smoluchowski theory for microelectrophoresis, is independent of particle shape and polydispersity. This makes it very attractive for practical use, with the hope that it might be as useful as classical Smoluchowski theory. In order to determine the kappa alpha range of the quasi-homogeneous model validity we develop the second version that limits ultrasound frequency, but applies no restriction on kappa alpha. The ultrasound frequency should substantially exceed the Maxwell-Wagner relaxation frequency. This limitation makes active conductivity related current negligible compared to the passive dielectric displacement current. It is possible to derive an expression for CVI in the concentrated dispersion as formulae inhering definite integrals with integrands depending on equilibrium potential distribution. This second version allowed us to estimate the ranges of the applicability of the first, quasi-homogeneous version. It turns out that the quasi-homogeneous model works for kappa alpha values up to almost 1. For instance, at volume fraction 30%, the highest kappa alpha limit of the quasi-homogeneous model is 0.65. Therefore, this version of the

Two-Dimensional Nucleation on the Terrace of Colloidal Crystals with Added Polymers.

Science.gov (United States)

Nozawa, Jun; Uda, Satoshi; Guo, Suxia; Hu, Sumeng; Toyotama, Akiko; Yamanaka, Junpei; Okada, Junpei; Koizumi, Haruhiko

2017-04-04

Understanding nucleation dynamics is important both fundamentally and technologically in materials science and other scientific fields. Two-dimensional (2D) nucleation is the predominant growth mechanism in colloidal crystallization, in which the particle interaction is attractive, and has recently been regarded as a promising method to fabricate varieties of complex nanostructures possessing innovative functionality. Here, polymers are added to a colloidal suspension to generate a depletion attractive force, and the detailed 2D nucleation process on the terrace of the colloidal crystals is investigated. In the system, we first measured the nucleation rate at various area fractions of particles on the terrace, ϕ area . In situ observations at single-particle resolution revealed that nucleation behavior follows the framework of classical nucleation theory (CNT), such as single-step nucleation pathway and existence of critical size. Characteristic nucleation behavior is observed in that the nucleation and growth stage are clearly differentiated. When many nuclei form in a small area of the terrace, a high density of kink sites of once formed islands makes growth more likely to occur than further nucleation because nucleation has a higher energy barrier than growth. The steady-state homogeneous 2D nucleation rate, J, and the critical size of nuclei, r*, are measured by in situ observations based on the CNT, which enable us to obtain the step free energy, γ, which is an important parameter for characterizing the nucleation process. The γ value is found to change according to the strength of attraction, which is tuned by the concentration of the polymer as a depletant.

Filtration of polydispersed colloids

International Nuclear Information System (INIS)

Nuttall, H.E.

1988-01-01

In this study, the dynamic microscopic form of the population balance model is applied to the problem of polydispersed particle capture in one spatial diffusion. This mathematical modeling approach can be applied to the difficult and potentially important problem of particulate (radiocolloid) transport in the groundwater surrounding a nuclear waste disposal site. To demonstrate the population balance methodology, the equations were developed and used to investigate transport and capture of polydispersed colloids in packed columns. Modeling simulations were compared to experimental column data. The multidimensional form of the population balance equation was used to analyze the transport and capture of polydispersed colloids. A numerical model was developed to describe transport of polydispersed colloids through a one-dimensional porous region. The effects of various size distributions were investigated in terms of capture efficiency. For simulating the column data, it was found by trial and error that as part of the population balance model a linear size dependent filtration function gave a good fit to the measured colloid concentration profile. The effects of constant versus size dependent filtration coefficients were compared and the differences illustrated by the calculated colloid profile within the column. Also observed from the model calculations was the dramatically changing liquid-phase colloid-size distribution which was plotted as a function of position down the column. This modeling approach was excellent for describing and understanding microscopic filtration in porous media

Effect of flexibility on the growth of concentration fluctuations in a suspension of sedimenting fibers: Particle simulations

Energy Technology Data Exchange (ETDEWEB)

Manikantan, Harishankar; Saintillan, David [Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, California 92093 (United States)

2016-01-15

Three-dimensional numerical simulations are performed to study the stability of a sedimenting suspension of weakly flexible fibers. It is well known that a suspension of rigid rods sedimenting under gravity at low Reynolds number is unstable to concentration fluctuations owing to hydrodynamic interactions. Flexible fibers, however, reorient while settling and even weak flexibility can alter their collective dynamics. In our recent work [Manikantan et al., “The instability of a sedimenting suspension of weakly flexible fibres,” J. Fluid Mech. 756, 935–964 (2014)], we developed a mean-field theory to predict the linear stability of such a system. Here, we verify these predictions using accurate and efficient particle simulations based on a slender-body model. We also demonstrate the mechanisms by which flexibility-induced reorientation alters suspension microstructure, and through it, its stability. Specifically, we first show that the anisotropy of the base state in the case of a suspension of flexible fibers has a destabilizing effect compared to a suspension of rigid rods. Second, a conflicting effect of flexibility is also shown to suppress particle clustering and slow down the growth of the instability. The relative magnitude of filament flexibility and rotational Brownian motion dictates which effect dominates, and our simulations qualitatively follow theoretically predicted trends. The mechanism for either effects is tied to the flexibility-induced reorientation of particles, which we illustrate using velocity and orientation statistics from our simulations. Finally, we also show that, in the case of an initially homogeneous and isotropic suspension, flexibility always acts to suppress the growth of the instability.

Effect of flexibility on the growth of concentration fluctuations in a suspension of sedimenting fibers: Particle simulations

International Nuclear Information System (INIS)

Manikantan, Harishankar; Saintillan, David

2016-01-01

Three-dimensional numerical simulations are performed to study the stability of a sedimenting suspension of weakly flexible fibers. It is well known that a suspension of rigid rods sedimenting under gravity at low Reynolds number is unstable to concentration fluctuations owing to hydrodynamic interactions. Flexible fibers, however, reorient while settling and even weak flexibility can alter their collective dynamics. In our recent work [Manikantan et al., “The instability of a sedimenting suspension of weakly flexible fibres,” J. Fluid Mech. 756, 935–964 (2014)], we developed a mean-field theory to predict the linear stability of such a system. Here, we verify these predictions using accurate and efficient particle simulations based on a slender-body model. We also demonstrate the mechanisms by which flexibility-induced reorientation alters suspension microstructure, and through it, its stability. Specifically, we first show that the anisotropy of the base state in the case of a suspension of flexible fibers has a destabilizing effect compared to a suspension of rigid rods. Second, a conflicting effect of flexibility is also shown to suppress particle clustering and slow down the growth of the instability. The relative magnitude of filament flexibility and rotational Brownian motion dictates which effect dominates, and our simulations qualitatively follow theoretically predicted trends. The mechanism for either effects is tied to the flexibility-induced reorientation of particles, which we illustrate using velocity and orientation statistics from our simulations. Finally, we also show that, in the case of an initially homogeneous and isotropic suspension, flexibility always acts to suppress the growth of the instability

Effective charge versus bare charge: an analytical estimate for colloids in the infinite dilution limit

International Nuclear Information System (INIS)

Aubouy, Miguel; Trizac, Emmanuel; Bocquet, Lyderic

2003-01-01

We propose an analytical approximation for the dependence of the effective charge on the bare charge for spherical and cylindrical macro-ions as a function of the size of the colloid and salt content, for the situation of a unique colloid immersed in a sea of electrolyte (where the definition of an effective charge is non-ambiguous). Our approach is based on the Poisson-Boltzmann (PB) mean-field theory. Mathematically speaking, our estimate is asymptotically exact in the limit κa >> 1, where a is the radius of the colloid and κ is the inverse screening length. In practice, a careful comparison with effective charge parameters, obtained by numerically solving the full nonlinear PB theory, proves that our estimate is good down to κa ∼ 1. This is precisely the limit appropriate to treat colloidal suspensions. A particular emphasis is put on the range of parameters suitable to describe both single and double strand DNA molecules under physiological conditions

Bentonite as a colloid source in groundwaters at Olkiluoto

International Nuclear Information System (INIS)

Vuorinen, U.; Hirvonen, H.

2005-02-01

In this work bentonite was studied as a potential source of colloids in Olkiluoto groundwaters. Samples were collected at two groundwater stations, PVA1 at 37.5 m dept and PVA3 at 95.6 m depth, in the VLJ-tunnel. The deeper groundwater at PVA3 was more saline (2.6g/L of Cl-) than the shallow at PVA1 (0.8g/L of Cl-). A bentonite source had been assembled at each groundwater station so that two sample lines were available for water samples; one for collecting a sample before and the other for collecting a sample after interaction with bentonite. Before starting the actual colloid sampling groundwaters from both sample lines at both stations were analysed. Only minor alterations, mostly within the uncertainty limits of the analysis methods, were brought about in the water chemistries after interaction with the bentonite sources. The only clear changes were seen in the concentration of iron which decreased after interaction with bentonite in the groundwaters at both stations. After groundwater sampling the actual colloid sampling was performed. The water samples were collected and treated inside a movable nitrogen filled glove-box. The samples could be collected from each sampling line directly in the glove-box via two quick-couplings that had been assembled on the front face of the box. The sample lines had been assembled with 0.45 μm filters before entering the glove-box, because only colloids smaller than 0.45 μm were of interest, as they are not prone to sedimentation in slow groundwater flows and therefore could act as potential radionuclide carriers. Colloid samples were collected and treated similarly from both sampling lines at both groundwater stations. For estimating the colloid content the groundwater samples were filtered with centrifugal ultrafiltration tubes of different cut-off values (0.3 μm, 300kD and 10kD). The ultrafiltrations produced the colloid-containing concentrate fractions and the soluble substances-containing filtrate fractions. In

Pair-correlations in swimmer suspensions

Science.gov (United States)

Nambiar, Sankalp; Subramanian, Ganesh

2017-11-01

Suspensions of rear-actuated swimming microorganisms, such as E.coli, exhibit several interesting phenomena including spontaneous pattern formation above a critical concentration, novel rheological properties, shear-induced concentration banding etc. Explanations based on mean-field theory are only qualitative, since interactions between swimmers are important for typical experimental concentrations. We analytically characterize the hydrodynamic pair-interactions in a quiescent suspension of slender straight swimmers. The pair-correlation, calculated at leading order by integrating the swimmer velocity disturbances along straight trajectories, decays as 1/r2 for r >> L (L being the swimmer size). This allows us to characterize both polar and nematic correlations in an interacting swimmer suspension. In the absence of correlations, the velocity covariance asymptotes from a constant for r > L, the latter being characteristic of a suspension of non-interacting point force-dipoles. On including correlations, the slow decay of the pair-orientation correlation leads to an additional contribution to the velocity covariance that diverges logarithmically with system size.

MD simulation of pair correlation function and static structure of charged colloidal suspensions

NARCIS (Netherlands)

Allahyarov, E.A.; Schram, P.P.J.M.; Trigger, S.A.

1996-01-01

On the basis of molecular dynamics the radial distribution function (r.d.f.) of colloidal plasma is calculated by using the effective macroion interaction in TPS-form. The vital importance of the minimum in the potential, which is a consequences of the strong counterion-macroion interaction, is

Two step continuous method to synthesize colloidal spheroid gold nanorods.

Science.gov (United States)

Chandra, S; Doran, J; McCormack, S J

2015-12-01

This research investigated a two-step continuous process to synthesize colloidal suspension of spheroid gold nanorods. In the first step; gold precursor was reduced to seed-like particles in the presence of polyvinylpyrrolidone and ascorbic acid. In continuous second step; silver nitrate and alkaline sodium hydroxide produced various shape and size Au nanoparticles. The shape was manipulated through weight ratio of ascorbic acid to silver nitrate by varying silver nitrate concentration. The specific weight ratio of 1.35-1.75 grew spheroid gold nanorods of aspect ratio ∼1.85 to ∼2.2. Lower weight ratio of 0.5-1.1 formed spherical nanoparticle. The alkaline medium increased the yield of gold nanorods and reduced reaction time at room temperature. The synthesized gold nanorods retained their shape and size in ethanol. The surface plasmon resonance was red shifted by ∼5 nm due to higher refractive index of ethanol than water. Copyright © 2015 Elsevier Inc. All rights reserved.

Collective hypersonic excitations in strongly multiple scattering colloids.

Science.gov (United States)

Still, T; Gantzounis, G; Kiefer, D; Hellmann, G; Sainidou, R; Fytas, G; Stefanou, N

2011-04-29

Unprecedented low-dispersion high-frequency acoustic excitations are observed in dense suspensions of elastically hard colloids. The experimental phononic band structure for SiO(2) particles with different sizes and volume fractions is well represented by rigorous full-elastodynamic multiple-scattering calculations. The slow phonons, which do not relate to particle resonances, are localized in the surrounding liquid medium and stem from coherent multiple scattering that becomes strong in the close-packing regime. Such rich phonon-matter interactions in nanostructures, being still unexplored, can open new opportunities in phononics.

Adsorption of ions by colloids in electrolyte solutions

International Nuclear Information System (INIS)

Kallay, N.

1977-01-01

The adsorption isotherm for ionic adsorption by colloid particles was evaluated. The adsorption process was treated as the reaction between colloid particles and ions. The colloid particle has been here considered as a reaction entity. The possibility of the surface potential determination was presented. The analyses of the experimental data showed, that (at electrolyte concentration higher than the critical coagulation one) the surface potential reaches its zero value

Colloids in the mortar backfill of a cementitious repository for radioactive waste

International Nuclear Information System (INIS)

Wieland, E.; Spieler, P.

1999-01-01

Colloids are present in groundwater aquifers and water-permeable engineered barrier systems and may facilitate the migration of radionuclides. A careful evaluation of colloid concentrations is required to assess the potential effect of colloids on nuclide migration and, consequently, on the safety of a repository for radioactive waste. A highly permeable mortar is foreseen to be used as backfill for the engineered barrier of the Swiss repository for low- and intermediate-level waste (L/ILW). The backfill is considered to be a chemical environment with a potential for colloid generation and, due to its high porosity, for colloid mobility. In this contribution a novel in-house built particle counting device is described, and measurements of colloid concentrations in the pore water of backfill mortar are presented. (author)

A New, General Strategy for Fabricating Highly Concentrated and Viscoplastic Suspensions Based on a Structural Approach To Modulate Interparticle Interaction.

Science.gov (United States)

Sakurai, Shunsuke; Kamada, Fuminori; Kobashi, Kazufumi; Futaba, Don N; Hata, Kenji

2018-01-24

We report a general strategy to fabricate highly concentrated, viscoplastic and stable suspensions by designing the particle surface structure to control the interparticle attractive forces. Unlike conventional methods, where the choice of solvent is critical in balancing interparticle interactions, suspensions showing excellent stability and viscoplastic properties were made using various solvents. We demonstrated this approach using highly sparse agglomerates of carbon nanotubes (CNTs) as the particles. Our results revealed that the essential feature of the CNT agglomerate to fabricate these suspensions was high porosity with a spacing size much smaller than the overall size, which was only possible using long single-walled carbon nanotubes (SWNTs). In this way, the agglomerate surface was characterized by fine network of CNT bundles. These suspensions exhibited solid-like behavior at rest (characterized by a high yield stress of c.a. 100 Pa) and a liquid-like behavior when subjected to a stress (characterized by a significant drop of an apparent viscosity to 1 Pa·s at a shear rate of 1000 s -1 ). Furthermore, in contrast to conventionally fabricated suspensions, these "CNT pastes" exhibited exceptional stability at rest, under flow, and at extremely high concentrations during the drying process, with only a weakly observable dependence on solvent type. As a result, highly uniform micrometer-thick SWNT films were successfully fabricated by dried blade-coated films of these pastes. Finally, we developed a simple, semiempirical model and clarified the importance of the CNT agglomerate microstructure (the ratio of spacing size/particle size and porosity) on tailoring the cohesive forces between particles to fabricate stable viscoplastic suspensions.

Microstructural Dynamics and Rheology of Suspensions of Rigid Fibers

Science.gov (United States)

Butler, Jason E.; Snook, Braden

2018-01-01

The dynamics and rheology of suspensions of rigid, non-Brownian fibers in Newtonian fluids are reviewed. Experiments, theories, and computer simulations are considered, with an emphasis on suspensions at semidilute and concentrated conditions. In these suspensions, interactions between the particles strongly influence the microstructure and rheological properties of the suspension. The interactions can arise from hydrodynamic disturbances, giving multibody interactions at long ranges and pairwise lubrication forces over short distances. For concentrated suspensions, additional interactions due to excluded volume (contacts) and adhesive forces are addressed. The relative importance of the various interactions as a function of fiber concentration is assessed.

Effect of Nitric Acid Concentrations on Synthesis and Stability of Maghemite Nanoparticles Suspension

Directory of Open Access Journals (Sweden)

Irwan Nurdin

2014-01-01

Full Text Available Maghemite (γ-Fe2O3 nanoparticles have been synthesized using a chemical coprecipitation method at different nitric acid concentrations as an oxidizing agent. Characterization of all samples performed by several techniques including X-ray diffraction (XRD, transmission electron microscopy (TEM, alternating gradient magnetometry (AGM, thermogravimetric analysis (TGA, dynamic light scattering (DLS, and zeta potential. The XRD patterns confirmed that the particles were maghemite. The crystallite size of all samples decreases with the increasing concentration of nitric acid. TEM observation showed that the particles have spherical morphology with narrow particle size distribution. The particles showed superparamagnetic behavior with decreased magnetization values at the increasing concentration of nitric acid. TGA measurement showed that the stability temperature decreases with the increasing concentration of nitric acid. DLS measurement showed that the hydrodynamic particle sizes decrease with the increasing concentration of nitric acid. Zeta potential values show a decrease with the increasing concentration of nitric acid. The increasing concentration of nitric acid in synthesis of maghemite nanoparticles produced smaller size particles, lower magnetization, better thermal stability, and more stable maghemite nanoparticles suspension.

Administrative license suspension: Does length of suspension matter?

Science.gov (United States)

Fell, James C; Scherer, Michael

2017-08-18

Administrative license revocation (ALR) laws, which provide that the license of a driver with a blood alcohol concentration at or over the illegal limit is subject to an immediate suspension by the state department of motor vehicles, are an example of a traffic law in which the sanction rapidly follows the offense. The power of ALR laws has been attributed to how swiftly the sanction is applied, but does the length of suspension matter? Our objectives were to (a) determine the relationship of the ALR suspension length to the prevalence of drinking drivers relative to sober drivers in fatal crashes and (b) estimate the extent to which the relationship is associated to the general deterrent effect compared to the specific deterrent effect of the law. Data comparing the impact of ALR law implementation and ALR law suspension periods were analyzed using structural equation modeling techniques on the ratio of drinking drivers to nondrinking drivers in fatal crashes from the Fatality Analysis Reporting System (FARS). States with an ALR law with a short suspension period (1-30 days) had a significantly lower drinking driver ratio than states with no ALR law. States with a suspension period of 91-180 days had significantly lower ratios than states with shorter suspension periods, while the three states with suspension lengths of 181 days or longer had significantly lower ratios than states with shorter suspension periods. The implementation of any ALR law was associated with a 13.1% decrease in the drinking/nondrinking driver fatal crash ratio but only a 1.8% decrease in the intoxicated/nonintoxicated fatal crash ratio. The ALR laws and suspension lengths had a significant general deterrent effect, but no specific deterrent effect. States might want to keep (or adopt) ALR laws for their general deterrent effects and pursue alternatives for specific deterrent effects. States with short ALR suspension periods should consider lengthening them to 91 days or longer.

Dissociation behavior of Np(IV) from humic acid colloid

Energy Technology Data Exchange (ETDEWEB)

Iijima, K.; Tobitsuka, S. [Japan Nuclear Cycle Development Institute, 4-33 Muramatsu, Tokai, Naka-gun, Ibaraki 319-1194 (Japan); Kohara, Y. [Inspection Development Corporation, 4-33, Muramatsu, Tokai, Nakagun, Ibaraki 319-1112 (Japan)

2005-07-01

Full text of publication follows: Dissociation behavior of Np(IV) from humic colloid, which was prepared with purified Aldrich humic acid (PAHA) was investigated. The complexation experiments were carried out in 0.1 M NaClO{sub 4} - 0.05 M Na{sub 2}S{sub 2}O{sub 4} solution at pH 8 with PAHA concentration between 0 and 500 mg L-1 under anaerobic condition. Np-237 was added as Np(V) solution so that its concentration becomes 1.1 x 10-5 mol L-1. After shaking from 1 to 156 days, aliquots of experimental solution were filtered through the membranes with 50, 10 and 3 kD of MWCO to obtain the size distribution of colloid, followed by adding the filtrate into the 6 M HCl for dissociation. At the end of experiments for 596 days, 0.1 M NaHCO{sub 3} was used for dissociation solution. The concentration of Np released into this solution was evaluated by measuring a activity of Np-237. The concentration of Np becomes constant by 112 days. Since Eh of the solution has been kept between -300 and -100 mV vs. SHE during experimental duration, Np is presumed to be reduced into tetravalent. In the case of higher PAHA concentration than 50 mg L{sup -1}, the Np concentration is close to that of initially added Np. Since the size of the dissolved species of Np during complexation experiments varies from 3 to 50 kD, the Np is sorbed on humic acid colloid. In the dissociation experiments, the Np dissociated by 6 M HCl decreases with increasing complexation time and PAHA concentration. After 156 days complexation with 500 mg L{sup -1} of PAHA, 35% of Np can be dissociated from the colloid. Such a tendency, however, is not observed in case of the lowest PAHA concentration, 5 mg L{sup -1}. After 596 days complexation, the dissociation experiments were carried out by adding 0.1 M NaHCO{sub 3} solution to avoid the precipitation which might hinder the dissociation of Np in the aforementioned experiments with HCl. As a result, 50% of Np is dissociated in the presence of 50 and 100 mg L-1 of

The use of synthetic Zn-/Ni-labeled montmorillonite colloids as a natural bentonite marker

International Nuclear Information System (INIS)

Huber, F.; Heck, S.; Hoess, P.; Bouby, M.; Schaefer, T.; Truche, L.; Brendle, J.

2012-01-01

Document available in extended abstract form only. Quantification of bentonite erosion rates/colloid release rates and the colloid attachment under unfavourable conditions for clay colloids is frequently based on the detection of the alumino-silicate building blocks and accompanied by relative high analytical uncertainties due to the presence of high background concentrations in the groundwater. In situ experiments planned at the Grimsel Test Site (CH) in the frame of the Colloid Formation and Migration (CFM) project foresee the emplacement of a compacted bentonite source and determination of the bentonite erosion rate under near-natural flow conditions. To univocally differentiate between the natural background colloid concentration and the eroded bentonite an irreversible labeling of the bentonite colloid source placed in a granite fracture would greatly improve their detection and reduce the analytical uncertainty. It is thought to use an admixture to label the natural bentonite. Therefore, the characteristics as erosion behavior, colloid stability and radionuclide sorption/reversibility behavior have to be studied and compared. Here, we focus on the radionuclide sorption reversibility. Synthetic montmorillonite containing structurally bound Zn and Ni in its octahedral layer was used within this study. Actually, Zn and Ni are good candidates to determine more accurately the colloid concentration as the ICP-MS sensitivity is at least one order of magnitude higher and the Zn and Ni background concentrations found in natural ground waters (e.g. Grimsel ground water, GGW) are very low. In the present study, the colloids are first separated and characterized by AsFlFFF-ICP-MS. Then, they are used to perform radionuclide reversibility kinetic experiments similar to those already published under anoxic conditions and room temperature. The aim is to compare the results obtained with those already available on natural FEBEX bentonite derived colloids. The size

Distribution of cesium between colloid-rock phases-establishment of experimental system and investigation of Cs distribution between colloid and rock

International Nuclear Information System (INIS)

Nakata, Kotaro

2006-01-01

Distribution and re-distribution of cesium between 3-phases (colloid, rock and water) was investigated. Analcite and bentonite colloid ware used as colloid phase and muscovite was used as rock phase. Before investigating the distribution between 3-phases, sorption and desorption behavior of Cs on analcite colloid, bentonite colloid and muscovite was investigated. It was found some fraction of Cs sorbed irreversibly on analcite colloid, while Cs sorbed reversibly on bentonite colloid. The experimental system was established for assessment of the distribution of nuclides between 3-phases by using combination of membrane filter and experimental cell. Since colloid and muscovite were separated by membrane filter, sorption of colloid on muscovite could be prevented and we could obtain distribution of Cs as ion. The distribution of Cs between 3-phases were obtained by this experimental system. Furthermore, re-distribution experiment was also carried out by using this system. After 7 days contact of colloid with Cs, distribution of sorbed Cs on colloid to liquid or muscovite phase was investigated. Comparing sorption and desorption isotherm with the distribution of Cs between 3-phases, it was found that Kd value of colloid (ratio of Cs concentration in liquid phase to amount of sorbed Cs on colloid phase) estimated in 2-phases (water and colloid) is different from that in 3-phases. Furthermore, in the case of analcite colloid, Kd value of colloid obtained in 3-phases distribution experiment was different from that obtained in re-distribution experiment. This is considered because of the irreversibility of Cs sorption on analcite colloid. Thus, it was found distribution of Cs in 3-phases was not predictable from sorption and desorption isotherm or Kd value of 2-phases (water-rock, water-colloid). (author)

THE INFLUENCES OF Fe(III ION and Fe(OH3 COLLOID ON THE PHOTODEGRADATION of p-CHLOROPHENOL CATALYZED BY TiO2

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Endang Tri Wahyuni

2010-06-01

Full Text Available The influences of ionic Fe(III and colloidal Fe(OH3 on the effectiveness of p-chlorophenol photodegradation catalyzed by TiO2 has been studied. Photodegradation was carried out in a batch system by irradiating a suspension of TiO2, p-chlorophenol, and Fe(III as ionic or colloidal forms, using UV lamp for a period of time accompanied by magnetic stirring. Concentration of photodegraded p-chlorophenol was calculated by subtracting the initial concentration with that of undegraded p-chlorophenol. Concentration of undegraded p-chlorophenol was determined by gas chromatography. In this study, TiO2 mass and the photodegradation time were optimized. The influences of concentration of Fe(III solution, mass of Fe(OH3, and pH of the solution have also been systematically studied. The research results showed that the presence of Fe(III ions improved the effectiveness of photocatalytical degradation of p-chlorophenol, which was proportional to the concentrations of Fe(III ion. In contrast, the increasing mass of Fe(OH3 led to a decrease in the degree of p-chlorophenol photodegradation. Furthermore, it was observed that increasing pH of the solution resulted in a decrease in the photodegradation of p-chlorophenol. This phenomena may be due to the different species of TiO2 available at the surface of photocatalyst and of ionic Fe(III and colloidal Fe(OH3 in the solution resulted from the pH alteration. The highest photodegradation degree, ca. 80 % was obtained when 20 mg of TiO2 was applied in the photodegradation of 50 mL of 100 ppm p-chlorophenol solution in the presence of 100 ppm Fe3+ irradiated by UV-light for 25 hours.    Keywords: p-chlorophenol photodegradation, TiO2, Fe(III species

Comparison of different filtration techniques for the pre-concentration of natural colloidal dispersions for field-flow-fractionation (FFF); Vergleich verschiedener Filtrationstechniken zur Aufkonzentrierung natuerlicher kolloidaler Dispersionen fuer die Feld-Fluss-Fraktionierung (FFF)

Energy Technology Data Exchange (ETDEWEB)

Saal, C.; Kammer, F. v.d. [Technische Univ. Hamburg-Harburg, Arbeitsbereich Umweltschutztechnik, Hamburg (Germany)

2002-07-01

The objektive of this study was to compare different pre-treatment techniques (active and passive filtration techniques applying various membranes) for field-flow-fractionation (FFF) analysis of natural aquatic colloids. In most cases FFF of natural water samples requires a pre-concentration step prior to analysis. The used FFF-method with online multi-detector-analysis (MDA) is a versatile method to specify the size distribution of particles (> 10 nm) in aqueous systems. Coupling FFF with trace element analysis (e. g. ICP-MS or total reflextion X-ray fluorescence (TXRF)) is a possibility for the determination of element/ size distributions. Analysing natural water samples with FFF a sample pre-treatment is needed in most cases, which can be a coarse filtration (> 5 {mu}m) to separate algea from the sample and a preconcentration of the colloidal fraction. The pre-treatment of the sample has to assure a minimum loss of colloidal particulate matter (CPM) and no change of size distribution. The different pre-concentration techniques were tested with water extractable soil colloids. We have developed methods with concentration factors F < 50 showing minor effects on the colloidal composition of the sample, so that these methods can be used to concentrate CPM of natural waters for size- and trace metal analysis. (orig.)

THE COLLOIDAL BEHAVIOR OF EDESTIN

Science.gov (United States)

Hitchcock, David I.

1922-01-01

1. It has been shown by titration experiments that the globulin edestin behaves like an amphoteric electrolyte, reacting stoichiometrically with acids and bases. 2. The potential difference developed between a solution of edestin chloride or acetate separated by a collodion membrane from an acid solution free from protein was found to be influenced by salt concentration and hydrogen ion concentration in the way predicted by Donnan's theory of membrane equilibrium. 3. The osmotic pressure of such edestin-acid salt solutions was found to be influenced by salt concentration and by hydrogen ion concentration in the same way as is the potential difference. 4. The colloidal behavior of edestin is thus completely analogous to that observed by Loeb with gelatin, casein, and egg albumin, and may be explained by Loeb's theory of colloidal behavior, which is based on the idea that proteins react stoichiometrically as amphoteric electrolytes and on Donnan's theory of membrane equilibrium. PMID:19871959

Small-angle neutron scattering from colloidal dispersions

International Nuclear Information System (INIS)

Ottewill, R.H.

1991-01-01

A survey is given of recent work on the use of small-angle neutron scattering to examine colloidal dispersions. Particular attention is given to the determination of particle size and polydispersity, the determination of particle morphology and the behaviour of concentrated colloidal dispersions, both at rest and under the influence of an applied shear field. (orig.)

Review on influences of colloids on geologic disposal of high level radioactive waste. For better understanding of natural colloidal materials

International Nuclear Information System (INIS)

Kanai, Yutaka; Suzuki, Masaya; Kamioka, Hikari; Yoshida, Takahiro; Suko, Takeshi

2007-01-01

Although the influences of colloidal materials on radionuclide transport in geological media are pointed out, their behaviors in natural environment have not yet been well elucidated and therefore their influences on the geologic disposal of high-level radioactive waste (HLW) are not fully estimated quantitatively. This paper reviewed the studies on natural colloids, especially focused on inorganic, organic and biological colloids, and discussed the future works to be carried out. Much attention should be paid to the sampling and analysis. Excellent techniques for in-situ observation, concentration without changing the state of colloid, standard procedure for analysis, are necessary to be developed. More research studies on the behaviors of colloids are required in not only far- and near-fields but also items on effects of the environments and its evolution. (author)

Bottom concentrations Determination of particle material in suspension in Medellin City

International Nuclear Information System (INIS)

Echeverri Londono, Carlos Alberto

2000-01-01

The aim of this work is at achieving a better understanding of background concentrations of particle materials in suspension (pst) in Medellin. This will allow certain actions and programs for watching and controlling air pollution in this city. Metals analyzed in particle material were: calcium, chromium, copper, iron, magnesium, nickel and lead. Chromium and nickel were not detected in any station and lead was detected in one station only. It is observed that all metals have a large dispersion, excepting total iron in La America and magnesium in point 2 at Belencito, which demonstrates the high temporal variability of these metals in these places. also It is observed that metals do not have a homogenous variation in their breathable fraction (encountered in pm-10) in relation to the total metals (encountered in PST) which is indication of the different sources contribution to the metals concentration and, in general, of PST and PM - 10

Tangential Flow Ultrafiltration Allows Purification and Concentration of Lauric Acid-/Albumin-Coated Particles for Improved Magnetic Treatment.

Science.gov (United States)

Zaloga, Jan; Stapf, Marcus; Nowak, Johannes; Pöttler, Marina; Friedrich, Ralf P; Tietze, Rainer; Lyer, Stefan; Lee, Geoffrey; Odenbach, Stefan; Hilger, Ingrid; Alexiou, Christoph

2015-08-14

Superparamagnetic iron oxide nanoparticles (SPIONs) are frequently used for drug targeting, hyperthermia and other biomedical purposes. Recently, we have reported the synthesis of lauric acid-/albumin-coated iron oxide nanoparticles SEON(LA-BSA), which were synthesized using excess albumin. For optimization of magnetic treatment applications, SPION suspensions need to be purified of excess surfactant and concentrated. Conventional methods for the purification and concentration of such ferrofluids often involve high shear stress and low purification rates for macromolecules, like albumin. In this work, removal of albumin by low shear stress tangential ultrafiltration and its influence on SEON(LA-BSA) particles was studied. Hydrodynamic size, surface properties and, consequently, colloidal stability of the nanoparticles remained unchanged by filtration or concentration up to four-fold (v/v). Thereby, the saturation magnetization of the suspension can be increased from 446.5 A/m up to 1667.9 A/m. In vitro analysis revealed that cellular uptake of SEON(LA-BSA) changed only marginally. The specific absorption rate (SAR) was not greatly affected by concentration. In contrast, the maximum temperature Tmax in magnetic hyperthermia is greatly enhanced from 44.4 °C up to 64.9 °C by the concentration of the particles up to 16.9 mg/mL total iron. Taken together, tangential ultrafiltration is feasible for purifying and concentrating complex hybrid coated SPION suspensions without negatively influencing specific particle characteristics. This enhances their potential for magnetic treatment.

Towards conducting inks: Polypyrrole–silver colloids

International Nuclear Information System (INIS)

Omastová, Mária; Bober, Patrycja; Morávková, Zuzana; Peřinka, Nikola; Kaplanová, Marie; Syrový, Tomáš; Hromádková, Jiřina; Trchová, Miroslava; Stejskal, Jaroslav

2014-01-01

Graphical abstract: - Highlights: • Composite colloidal particles combining conducting polymer and metal have been prepared. • Conducting colloids are suitable for printing applications. • Polypyrrole/silver colloids are prepared in a single reaction step. • The conductivity control is discussed and still needs improvement. - Abstract: The oxidation of pyrrole with silver nitrate in the presence of suitable water-soluble polymers yields composite polypyrrole–silver colloids. The polypyrrole–silver nanoparticles stabilized with poly(N-vinylpyrrolidone) have a typical size around 350 nm and polydispersity index 0.20, i.e. a moderate polydispersity in size. Similar results have been obtained with poly(vinyl alcohol) as stabilizer. The effect of stabilizer concentration on the particle size is marginal. In the present study, several types of stabilizers have been tested in addition to currently used poly(N-vinylpyrrolidone). Transmission electron microscopy and optical microscopy revealed the gemini morphology of polypyrrole and silver colloidal nanoparticles and confirmed their size and size-distribution determined by dynamic light scattering. The use of colloidal dispersions provides an efficient tool for the UV–vis and FT Raman spectroscopic characterization of polypyrrole, including the transition between polypyrrole salt and corresponding polypyrrole base. The dispersions were used for the preparation of coatings on polyethylene terephthalate foils, and the properties for polypyrrole–silver composites have been compared with those produced from polypyrrole colloids alone

Comparison of photon correlation spectroscopy with photosedimentation analysis for the determination of aqueous colloid size distributions

Science.gov (United States)

Rees, Terry F.

1990-01-01

Colloidal materials, dispersed phases with dimensions between 0.001 and 1 μm, are potential transport media for a variety of contaminants in surface and ground water. Characterization of these colloids, and identification of the parameters that control their movement, are necessary before transport simulations can be attempted. Two techniques that can be used to determine the particle-size distribution of colloidal materials suspended in natural waters are compared. Photon correlation Spectroscopy (PCS) utilizes the Doppler frequency shift of photons scattered off particles undergoing Brownian motion to determine the size of colloids suspended in water. Photosedimentation analysis (PSA) measures the time-dependent change in optical density of a suspension of colloidal particles undergoing centrifugation. A description of both techniques, important underlying assumptions, and limitations are given. Results for a series of river water samples show that the colloid-size distribution means are statistically identical as determined by both techniques. This also is true of the mass median diameter (MMD), even though MMD values determined by PSA are consistently smaller than those determined by PCS. Because of this small negative bias, the skew parameters for the distributions are generally smaller for the PCS-determined distributions than for the PSA-determined distributions. Smaller polydispersity indices for the distributions are also determined by PCS.

Irreversible colloidal agglomeration in presence of associative inhibitors: Computer simulation study

International Nuclear Information System (INIS)

Barcenas, Mariana; Duda, Yurko

2007-01-01

Monte Carlo simulation is employed to study the irreversible particle-cluster agglomeration of valence-limited colloids affected by associative inhibitors. The cluster size distribution and number of connections between colloids are analyzed as a function of density and inhibitor concentration. The influence of colloid functionality on its aggregation is discussed

Transport of Silica Colloid through Saturated Porous Media under Different Hydrogeochemical and Hydrodynamic Conditions Considering Managed Aquifer Recharge

Directory of Open Access Journals (Sweden)

Zhuo Wang

2016-11-01

Full Text Available Colloids may have an important role in regulating the structure and function of groundwater ecosystems, and may influence the migration of low solubility contaminants in groundwater. There is, however, a degree of uncertainty about how colloids behave under the variable hydrogeochemical and hydrodynamic conditions that occur during managed aquifer recharge. We used an online monitoring system to monitor the transport of silica colloid in saturated porous media under different hydrogeochemical conditions, including a range of pH values (5, 7, and 9, ionic strengths (<0.0005, 0.02, and 0.05 M, cation valences (Na+, Ca2+, flow rates (0.1, 0.2, and 0.4 mL/min. The results showed that silica colloid was more likely to deposit on the surface of porous media in acidic conditions (pH = 5 than in alkaline conditions (pH = 9, indicating that the risks of pollution from colloidal interactions would be higher when the pH of the recharge water was higher. Colloid deposition occurred when the ionic strength of the colloidal suspension increased, and bivalent cations had a greater effect than monovalent cations. This suggests that bivalent cation-rich recharge water might affect the porosity of the porous medium because of colloid deposition during the managed aquifer recharge process. As the flow rate increased, the migration ability of silica colloid increased. We simulated the migration of silica colloid in porous media with the COMSOL Multiphysics model.

Formation, characterization, and stability of plutonium (IV) colloid

International Nuclear Information System (INIS)

Hobart, D.E.; Morris, D.E.; Palmer, P.D.; Newton, T.W.

1989-01-01

Plutonium is expected to be a major component of the waste element package in any high-level nuclear waste repository. Plutonium(IV) is known to form colloids under chemical conditions similar to those found in typical groundwaters. In the event of a breach of a repository, these colloids represent a source of radionuclide transport to the far-field environment, in parallel with the transport of dissolved waste element species. In addition, the colloids may decompose or disaggregate into soluble ionic species. Thus, colloids represent an additional term in determining waste element solubility limits. A thorough characterization of the physical and chemical properties of these colloids under relevant conditions is essential to assess the concentration limits and transport mechanisms for the waste elements at the proposed Yucca Mountain Repository site. This report is concerned primarily with recent results obtained by the Yucca Mountain Project (YMP) Solubility Determination Task pertaining to the characterization of the structural and chemical properties of Pu(IV) colloid. Important results will be presented which provides further evidence that colloidal plutonium(IV) is structurally similar to plutonium dioxide and that colloidal plutonium(IV) is electrochemically reactive. 13 refs., 7 figs

Colloid mobilization and heavy metal transport in the sampling of soil solution from Duckum soil in South Korea.

Science.gov (United States)

Lee, Seyong; Ko, Il-Won; Yoon, In-Ho; Kim, Dong-Wook; Kim, Kyoung-Woong

2018-03-24

Colloid mobilization is a significant process governing colloid-associated transport of heavy metals in subsurface environments. It has been studied for the last three decades to understand this process. However, colloid mobilization and heavy metal transport in soil solutions have rarely been studied using soils in South Korea. We investigated the colloid mobilization in a variety of flow rates during sampling soil solutions in sand columns. The colloid concentrations were increased at low flow rates and in saturated regimes. Colloid concentrations increased 1000-fold higher at pH 9.2 than at pH 7.3 in the absence of 10 mM NaCl solution. In addition, those were fourfold higher in the absence than in the presence of the NaCl solution at pH 9.2. It was suggested that the mobility of colloids should be enhanced in porous media under the basic conditions and the low ionic strength. In real field soils, the concentrations of As, Cr, and Pb in soil solutions increased with the increase in colloid concentrations at initial momentarily changed soil water pressure, whereas the concentrations of Cd, Cu, Fe, Ni, Al, and Co lagged behind the colloid release. Therefore, physicochemical changes and heavy metal characteristics have important implications for colloid-facilitated transport during sampling soil solutions.

Sorption and mechanism of aqueous U(Ⅵ) onto red soil-colloid

International Nuclear Information System (INIS)

Xia Liangshu; Huang Xin; Cao Cuncun; Chen Wei; Lu Junwen

2013-01-01

By static adsorption experiments, the effects of pH, ionic strength, adsorption time, uranium initial concentration, adsorbent dosage, red soil-colloid size, and organic matters on the biosorption capacity of red soil-colloid extracted from the soil around uranium tailing for uranium were studied. The adsorption process was analyzed by thermodynamics and kinetics, and the adsorption mechanism was characterized by the element analysis, infrared spectroscopy and scanning electron microscopy. The results show that the adsorption capacity for U (Ⅵ) on red soil-colloid increases with the decrease of ionic strength or particle size, increases with the initial concentration of uranium, decreases with the increase of the amount of red soil-colloid; the saturated adsorption capacity q max can be up to 76.76 μg/mg by red soil-colloid which diameter is less than 1 μm at 25 ℃ and pH=3.5, when the ionic strength is 0.001 mol/L. FT-IR micrograph before and after red soil-colloid adsorbed uranyl ions indicates that the red soil-colloid are mainly composed of hydroxyl, carbonyl, Si-O, Si-O-Fe, etc. The adsorption of U (Ⅵ) on red soil-colloid follows Langmuir adsorption isotherm, and the pseudo-second-order equation provides the best correlation for the adsorption process. (authors)

Diffusing colloidal probes of protein-carbohydrate interactions.

Science.gov (United States)

Eichmann, Shannon L; Meric, Gulsum; Swavola, Julia C; Bevan, Michael A

2013-02-19

We present diffusing colloidal probe measurements of weak, multivalent, specific protein-polysaccharide interactions mediated by a competing monosaccharide. Specifically, we used integrated evanescent wave and video microscopy methods to monitor the three-dimensional Brownian excursions of conconavilin A (ConA) decorated colloids interacting with dextran-functionalized surfaces in the presence of glucose. Particle trajectories were interpreted as binding lifetime histograms, binding isotherms, and potentials of mean force. Binding lifetimes and isotherms showed clear trends of decreasing ConA-dextran-specific binding with increasing glucose concentration, consistent with expectations. Net potentials were accurately captured by superposition of a short-range, glucose-independent ConA-dextran repulsion and a longer-range, glucose-dependent dextran bridging attraction modeled as a harmonic potential. For glucose concentrations greater than 100 mM, the net ConA-dextran potential was found to have only a nonspecific repulsion, similar to that of bovine serum albumin (BSA) decorated colloids over dextran determined in control experiments. Our results demonstrate the first use of optical microscopy methods to quantify the connections between potentials of mean force and the binding behavior of ConA-decorated colloids on dextran-functionalized surfaces.

Cation colloidal particles in alkaline-earth halides

Energy Technology Data Exchange (ETDEWEB)

Alcala, R; Orera, V M [Zaragoza Univ. (Spain). Facultad da Ciencias

1976-01-01

The formation of calcium, strontium and barium colloids both in heavily electron irradiated samples and in additively colored crystals of CaF/sub 2/, SrF/sub 2/ and BaF/sub 2/ has been investigated. Detailed data on the temperature dependence of the efficiency of colloid formation by irradiation have been obained. The growth of metallic particles in additively colored samples containing F and M centers has been studied for different color center concentrations and annealing temperatures. The optical absorption bands due to metallic colloids have been calculated using the theory of Mie. To take account of the pressure exerted by the matrix on the metallic particles several corrections to the optical constants of the metals have been introduced. A good agreement between theoretical calculations and experimental results has been obtained. The evolution of colloids along several thermal annealing experiments has also been investigated. A diffusion-limited model has been used which accounts for the dependence of the colloid radii with the annealing time.

Extraction and characterisation of colloids in waste repository leachate

International Nuclear Information System (INIS)

Verrall, K.E.

1998-10-01

Inorganic colloids are ubiquitous in environmental waters and are thought to be potential transporters of radionuclides and other toxic metals. Colloids present large surface areas to pollutants and contaminants present in waters and are therefore capable of sorbing and transporting them via groundwater and surface water movement. Much research has been and is currently being undertaken to understand more fully the stability of colloids in different water chemistries, factors which affect metal sorption onto colloids, and the processes which affect metal-colloid transport. This thesis first investigates groundwater and surface water sampling and characterisation techniques for the investigation of the colloids present in and around a low-level waste repository. Samples were collected anaerobically using micro-purge low-flow methodology (MPLF) and then subjected to sequential ultrafiltration, again anaerobically. After separation into size fractions the solids were analysed for radiochemical content, colloid population and morphology. It was found that colloids were present in large numbers in the groundwaters extracted from the trench waste burial area (anaerobic environment), but in the surface drain waters (aerobic environment) colloid population was comparable to levels found in waters extracted from above the trenches. There was evidence that the non-tritium activity was associated with the colloids and particulates in the trenches, but outside of the trenches the evidence was not conclusive because the activity and colloid concentrations were low. Secondly this thesis investigates the stability of inorganic colloids, mainly haematite, in the presence of humic acid, varying pH and electrolyte concentrations. The applicability of the SchuIze-Hardy rule to haematite and haematite/humic acid mixtures was investigated using photon correlation spectroscopy to measure the rate of fast and slow coagulation after the addition of mono, di and trivalent ions. It was

Natural colloids in groundwater from granite and their potential impact on radionuclide transport

International Nuclear Information System (INIS)

Vilks, P.; Bachinski, D.B.

1997-03-01

AECL has submitted an Environmental Impact Statement (EIS) to evaluate the concept of nuclear fuel disposal at depth in crystalline rock of the Canadian Shield. As part of geochemical studies carried out in support of the EIS, the role of natural groundwater colloids (0.001 to 0.45 μm) and suspended particles (>0.45 μm) in radionuclide transport in granite rock has been investigated. This report summarizes the results of investigations carried out in groundwaters from the Whiteshell Research Area (WRA) of southern Manitoba and the Atikokan Research Area (ARA) of northwestern Ontario to determine the concentrations, size distributions, and compositions of natural particles in groundwaters from the Canadian Shield. Particles from groundwater were isolated by ultrafiltration under a nitrogen atmosphere and particle concentrations and size distributions were determined by filtration, and by laser-based particle counting and size analysis. Groundwaters from Canadian Shield granites contain particles in a broad range of sizes, with no one particular size being dominant. Particle compositions include aluminosilicates, Fe oxides, carbonate and organics. Suspended particles are most likely generated by the mobilization of fracture-lining minerals by groundwater flow, while colloids are formed by a combination of precipitation and mobilization of colloidal material from fracture surfaces. The average concentration of 0.01 to 0.45 μm colloids in WRA groundwaters was 1.05 ± 0.14 mg/L. Average colloid concentrations were slightly higher in the more highly fractured ARA, although the highest observed colloid concentration in the ARA was below the 7 mg/L maximum observed in a sample from the WRA. The existence of colloids in the 0.001 to 0.01 μm size range was demonstrated using the results of chemical analysis of particle concentrates and data obtained with the laser-based Ultrafine Particle Size Analyzer (UPA). The WRA groundwaters contain on average about 2.7 mg/L of 0

Engineering Multifunctional Living Paints: Thin, Convectively-Assembled Biocomposite Coatings of Live Cells and Colloidal Latex Particles Deposited by Continuous Convective-Sedimentation Assembly

Science.gov (United States)

Jenkins, Jessica Shawn

Advanced composite materials could be revolutionized by the development of methods to incorporate living cells into functional materials and devices. This could be accomplished by continuously and rapidly depositing thin ordered arrays of adhesive colloidal latex particles and live cells that maintain stability and preserve microbial reactivity. Convective assembly is one method of rapidly assembling colloidal particles into thin (advantages over thicker randomly ordered composites, including enhanced cell stability and increased reactivity through minimized diffusion resistance to nutrients and reduced light scattering. This method can be used to precisely deposit live bacteria, cyanobacteria, yeast, and algae into biocomposite coatings, forming reactive biosensors, photoabsorbers, or advanced biocatalysts. This dissertation developed new continuous deposition and coating characterization methods for fabricating and characterizing 90 hours) photohydrogen production under anoxygenic conditions. Nutrient reduction slows cell division, minimizing coating outgrowth, and promotes photohydrogen generation, improving coating reactivity. Scanning electron microscopy of microstructure revealed how coating reactivity can be controlled by the size and distribution of the nanopores in the biocomposite layers. Variations in colloid microsphere size and suspension composition do not affect coating reactivity, but both parameters alter coating microstructure. Porous paper coated with thin coatings of colloidal particles and cells to enable coatings to be used in a gas-phase without dehydration may offer higher volumetric productivity for hydrogen production. Future work should focus on optimization of cell density, light intensity, media cycling, and acetate concentration.

Sensitive chemical neutron dosimetry using silver colloids

International Nuclear Information System (INIS)

Brede, O.; Boes, J.; Hoesselbarth, B.

1982-01-01

The radiation-induced formation of silver colloid was checked for its use as a sensitive dosimeter for neutron irradiation. For non-monoenergetic pulsed neutron irradiation in the Dubna IBR-30 reactor, the colloid dosimeter was found to be suitable to indicate the chemical neutron effect, i.e., to determine the sum concentration of the primary particles of water radiolysis: esub(aq)sup(-), OH and H. (author)

Field-effect measurements of mobility and carrier concentration of Cu2S colloidal quantum dot thin films after ligand exchange

International Nuclear Information System (INIS)

Brewer, Adam S.; Arnold, Michael S.

2014-01-01

Colloidal quantum dots (CQDs) of copper sulfide (Cu 2 S), an earth-abundant semiconductor, have a number of intriguing applications that require knowledge of their electrical properties. Depending on stoichiometry, mobility, and surface treatment, applications include photoabsorbers for solar cells, tunable plasmonics, and counter-electrodes for polysulfate electrolytes. However, there have not been any direct measurements of electrical properties in Cu 2 S CQD thin films. Here, we exchange as synthesized dodecanethiol ligands with short ethanedithiol or ethylenediamine ligands to form thin films of coupled Cu 2 S CQDs. The mobility and carrier concentration were found to vary by ligand treatment from 10 −5 cm 2 /Vs and 10 19 holes/cm 3 for ethanedithiol ligands to 10 −3 cm 2 /Vs and 10 20 holes/cm 3 for ethylenediamine. These results are consistent with the carrier concentrations inferred from sub-bandgap surface-plasmon-resonances measured by infrared spectroscopy. These results will be useful when designing Cu 2 S materials for future applications. - Highlights: • Colloidal Cu2S quantum dots were synthesized and characterized. • Ligand exchange was performed to alter the Cu2S nanocrystal properties. • Ligand exchange was studied using photoluminescence and infrared spectroscopy. • Field effect mobility and carrier concentration were directly measured. • Carrier concentration was compared to estimates from surface plasmon resonances

Implications of the effective one-component analysis of pair correlations in colloidal fluids with polydispersity

Science.gov (United States)

Pond, Mark J.; Errington, Jeffrey R.; Truskett, Thomas M.

2011-09-01

Partial pair-correlation functions of colloidal suspensions with continuous polydispersity can be challenging to characterize from optical microscopy or computer simulation data due to inadequate sampling. As a result, it is common to adopt an effective one-component description of the structure that ignores the differences between particle types. Unfortunately, whether this kind of simplified description preserves or averages out information important for understanding the behavior of the fluid depends on the degree of polydispersity and can be difficult to assess, especially when the corresponding multicomponent description of the pair correlations is unavailable for comparison. Here, we present a computer simulation study that examines the implications of adopting an effective one-component structural description of a polydisperse fluid. The square-well model that we investigate mimics key aspects of the experimental behavior of suspended colloids with short-range, polymer-mediated attractions. To characterize the partial pair-correlation functions and thermodynamic excess entropy of this system, we introduce a Monte Carlo sampling strategy appropriate for fluids with a large number of pseudo-components. The data from our simulations at high particle concentrations, as well as exact theoretical results for dilute systems, show how qualitatively different trends between structural order and particle attractions emerge from the multicomponent and effective one-component treatments, even with systems characterized by moderate polydispersity. We examine consequences of these differences for excess-entropy based scalings of shear viscosity, and we discuss how use of the multicomponent treatment reveals similarities between the corresponding dynamic scaling behaviors of attractive colloids and liquid water that the effective one-component analysis does not capture.

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

International Nuclear Information System (INIS)

Choi, Young Joon; Djilali, Ned

2016-01-01

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

Experimental studies on the inventory of cement-derived colloids in the pore water of a cementitious backfill material

International Nuclear Information System (INIS)

Wieland, E.

2001-06-01

The potential role of near-field colloids for the colloid-facilitated migration of radionuclides has stimulated investigations concerning the generation and presence of colloids in the near-field of a repository for low- and intermediate level waste (L/ILW). The highly gas permeable mortar (Nagra designation: mortar M1) is currently favoured as backfill material for the engineered barrier of the planned Swiss L/ILW repository. The cementitious backfill is considered to be a chemical environment with some potential for colloid generation. In a series of batch-style laboratory experiments the physico-chemical processes controlling the inventory of colloids in cement pore water of the backfill were assessed for chemical conditions prevailing in the initial stage of the cement degradation. In these experiments, backfill mortar M1 or quartz, respectively, which may be used as aggregate material for the backfill, were immersed in artificial cement pore water (a NaOH/KOH rich cement fluid). Colloid concentrations in the cement pore water were recorded as a function of time for different experimental settings. The results indicate that a colloid-colloid interaction process (coagulation) controlled the colloid inventory. The mass concentration of dispersed colloids was found to be typically lower than 0.02 ppm in undisturbed batch systems. An upper-bound value was estimated to be 0.1 ppm taking into account uncertainties on the measurements. To assess the potential for colloid generation in a dynamic system, colloid concentrations were determined in the pore water of a column filled with backfill mortar. The chemical conditions established in the mortar column corresponded to conditions observed in the second stage of the cement degradation (a Ca(OH) 2 - controlled cement system). In this dynamic system, the upper-bound value for the colloid mass concentration was estimated to be 0.1 ppm. Implications for radionuclide mobility were deduced taking into account the

Modeling of Hydrodynamic Chromatography for Colloid Migration in Fractured Rock

International Nuclear Information System (INIS)

Li Shihhai; Jen, C.-P.

2001-01-01

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

Microfluidic generation of droplets with a high loading of nanoparticles.

Science.gov (United States)

Wan, Jiandi; Shi, Lei; Benson, Bryan; Bruzek, Matthew J; Anthony, John E; Sinko, Patrick J; Prudhomme, Robert K; Stone, Howard A

2012-09-18

Microfluidic approaches for controlled generation of colloidal clusters, for example, via encapsulation of colloidal particles in droplets, have been used for the synthesis of functional materials including drug delivery carriers. Most of the studies, however, use a low concentration of an original colloidal suspension (60 wt %) particle concentrations. Three types of microfluidic devices, PDMS flow-focusing, PDMS T-junction, and microcapillary devices, are investigated for direct encapsulation of a high concentration of polystyrene (PS) nanoparticles in droplets. In particular, it is shown that PDMS devices fabricated by soft lithography can generate droplets from a 25 wt % PS suspension, whereas microcapillary devices made from glass capillary tubes are able to produce droplets from a 67 wt % PS nanoparticle suspension. When the PS concentration is between 0.6 and 25 wt %, the size of the droplets is found to change with the oil-to-water flow rate ratio and is independent of the concentration of particles in the initial suspensions. Drop sizes from ~12 to 40 μm are made using flow rate ratios Q(oil)/Q(water) from 20 to 1, respectively, with either of the PDMS devices. However, clogging occurs in PDMS devices at high PS concentrations (>25 wt %) arising from interactions between the PS colloids and the surface of PDMS devices. Glass microcapillary devices, on the other hand, are resistant to clogging and can produce droplets continuously even when the concentration of PS nanoparticles reaches 67 wt %. We believe that our findings indicate useful approaches and guidelines for the controlled generation of emulsions filled with a high loading of nanoparticles, which are useful for drug delivery applications.

Microfluidic generation of droplets with a high loading of nanoparticles

Science.gov (United States)

Wan, Jiandi; Shi, Lei; Benson, Bryan; Bruzek, Matthew J.; Anthony, John E.; Sinko, Patrick J.; Prudhomme, Robert K.; Stone, Howard A.

2012-01-01

Microfluidic approaches for controlled generation of colloidal clusters, e.g., via encapsulation of colloidal particles in droplets, have been used for the synthesis of functional materials including drug delivery carriers. Most of the studies, however, use a low concentration of an original colloidal suspension ( 60 wt%) particle concentrations. Three types of microfluidic devices, PDMS flow-focusing, PDMS T-junction, and microcapillary devices, are investigated for direct encapsulation of a high concentration of polystyrene (PS) nanoparticles in droplets. In particular, it is shown that PDMS devices fabricated by soft lithography can generate droplets from a 25 wt% PS suspension, whereas microcapillary devices made from glass capillary tubes are able to produce droplets from a 67 wt% PS nanoparticle suspension. When the PS concentration is between 0.6 and 25 wt%, the size of the droplets is found to change with the oil-to-water flow rate ratio and is independent of the concentration of particles in the initial suspensions. Drop sizes from ~12 to 40 μm are made using flow rate ratios Qoil/Qwater from 20 to 1, respectively, with either of the PDMS devices. However, clogging occurs in PDMS devices at high PS concentrations (> 25 wt%) arising from interactions between the PS colloids and the surface of PDMS devices. Glass microcapillary devices, on the other hand, are resistant to clogging and can produce droplets continuously even when the concentration of PS nanoparticles reaches 67 wt%. We believe that our findings indicate useful approaches and guidelines for the controlled generation of emulsions of microparticles that are filled with a high loading of nanoparticles and which are useful for drug delivery applications. PMID:22934976

Dispersions of Goethite Nanorods in Aprotic Polar Solvents

Directory of Open Access Journals (Sweden)

Delphine Coursault

2017-10-01

Full Text Available Colloidal suspensions of anisotropic nanoparticles can spontaneously self-organize in liquid-crystalline phases beyond some concentration threshold. These phases often respond to electric and magnetic fields. At lower concentrations, usual isotropic liquids are observed but they can display very strong Kerr and Cotton-Mouton effects (i.e., field-induced particle orientation. For many examples of these colloidal suspensions, the solvent is water, which hinders most electro-optic applications. Here, for goethite (α-FeOOH nanorod dispersions, we show that water can be replaced by polar aprotic solvents, such as N-methyl-2-pyrrolidone (NMP and dimethylsulfoxide (DMSO, without loss of colloidal stability. By polarized-light microscopy, small-angle X-ray scattering and electro-optic measurements, we found that the nematic phase, with its field-response properties, is retained. Moreover, a strong Kerr effect was also observed with isotropic goethite suspensions in these polar aprotic solvents. Furthermore, we found no significant difference in the behavior of both the nematic and isotropic phases between the aqueous and non-aqueous dispersions. Our work shows that goethite nanorod suspensions in polar aprotic solvents, suitable for electro-optic applications, can easily be produced and that they keep all their outstanding properties. It also suggests that this solvent replacement method could be extended to the aqueous colloidal suspensions of other kinds of charged anisotropic nanoparticles.

Colloids related to low level and intermediate level waste

International Nuclear Information System (INIS)

Ramsay, J.D.F.; Russell, P.J.; Avery, R.G.

1991-03-01

A comprehensive investigation has been undertaken to improve the understanding of the potential role of colloids in the context of disposal and storage of low and intermediate level waste immobilised in cement. Several topics have been investigated using a wide range of advanced physico-chemical and analytical techniques. These include: (a) the study of formation and characteristics of colloids in cement leachates, (b) the effects of the near-field aqueous chemistry on the characteristics of colloids in repository environments, (c) colloid sorption behaviour, (d) interactions of near-field materials with leachates, and (e) preliminary assessment of colloid migration behaviour. It has been shown that the generation of colloids in cement leachates can arise from a process of nucleation and growth leading to an amorphous phase which is predominantly calcium silicate hydrate. Such colloidal material has a capacity for association with polyvalent rare earths and actinides and these may be significant in the source term and processes involving radionuclide retention in the near field. It has also been shown that the near-field aqueous chemistry (pH, Ca 2+ concentration) has a marked effect on colloid behaviour (deposition and stability). A mechanistic approach to predict colloid sorption affinity has been developed which highlights the importance of colloid characteristics and the nature of the ionic species. (author)

Dissolved and colloidal trace elements in the Mississippi River delta outflow after Hurricanes Katrina and Rita

Science.gov (United States)

Shim, Moo-Joon; Swarzenski, Peter W.; Shiller, Alan M.

2012-07-01

The Mississippi River delta outflow region is periodically disturbed by tropical weather systems including major hurricanes, which can terminate seasonal bottom water hypoxia and cause the resuspension of shelf bottom sediments which could result in the injection of trace elements into the water column. In the summer of 2005, Hurricanes Katrina and Rita passed over the Louisiana Shelf within a month of each other. Three weeks after Rita, we collected water samples in the Mississippi River delta outflow, examining the distributions of trace elements to study the effect of Hurricanes Katrina and Rita. We observed limited stratification on the shelf and bottom waters that were no longer hypoxic. This resulted, for instance, in bottom water dissolved Mn being lower than is typically observed during hypoxia, but with concentrations still compatible with Mn-O2 trends previously reported. Interestingly, for no element were we able to identify an obvious effect of sediment resuspension on its distribution. In general, elemental distributions were compatible with previous observations in the Mississippi outflow system. Co and Re, which have not been reported for this system previously, showed behavior consistent with other systems: input for Co likely from desorption and conservative mixing for Re. For Cs, an element for which there is little information regarding its estuarine behavior, conservative mixing was also observed. Our filtration method, which allowed us to distinguish the dissolved (<0.02 μm) from colloidal (0.02-0.45 μm) phase, revealed significant colloidal fractions for Fe and Zn, only. For Fe, the colloidal phase was the dominant fraction and was rapidly removed at low salinity. Dissolved Fe, in contrast, persisted out to mid-salinities, being removed in a similar fashion to nitrate. This ability to distinguish the smaller Fe (likely dominantly organically complexed) from larger colloidal suspensates may be useful in better interpreting the bioavailablity

Study of conditions of production and characterization of noble metal micro-particles suspensions

International Nuclear Information System (INIS)

Malabre, Catherine

1983-01-01

As the production and identification of metal micro-particle suspensions are some aspects of issues related to nuclear fuel reprocessing, this research thesis reports the use of ruthenium, molybdenum, niobium, palladium and rhodium (fission metals) to generate such micro-particles. They are produced by erosion of two electrodes between which occurs an electric arc discharge in aqueous media. Different analytic methods are developed to determine the characteristics of so-produced colloidal solutions. A granulometry study is performed by transmission electronic microscopy, light quasi-elastic scattering, and turbidimetry associated to centrifugation. This has lead to the production of steady micro-particle suspensions which have been used in a first set of industrial trials [fr

Aqueous suspensions of natural swelling clay minerals. 2. Rheological characterization.

Science.gov (United States)

Paineau, Erwan; Michot, Laurent J; Bihannic, Isabelle; Baravian, Christophe

2011-06-21

We report in this article a comprehensive investigation of the viscoelastic behavior of different natural colloidal clay minerals in aqueous solution. Rheological experiments were carried out under both dynamic and steady-state conditions, allowing us to derive the elasticity and yield stress. Both parameters can be renormalized for all sizes, ionic strength, and type of clay using in a first approach only the volume of the particles. However, applying such a treatment to various clays of similar shapes and sizes yields differences that can be linked to the repulsion strength and charge location in the swelling clays. The stronger the repulsive interactions, the better the orientation of clay particles in flows. In addition, a master linear relationship between the elasticity and yield stress whose value corresponds to a critical deformation of 0.1 was evidenced. Such a relationship may be general for any colloidal suspension of anisometric particles as revealed by the analysis of various experimental data obtained on either disk-shaped or lath- and rod-shaped particles. The particle size dependence of the sol-gel transition was also investigated in detail. To understand why suspensions of larger particles gel at a higher volume fraction, we propose a very simplified view based on the statistical hydrodynamic trapping of a particle by an another one in its neighborhood upon translation and during a short period of time. We show that the key parameter describing this hydrodynamic trapping varies as the cube of the average diameter and captures most features of the sol-gel transition. Finally, we pointed out that in the high shear limit the suspension viscosity is still closely related to electrostatic interactions and follows the same trends as the viscoelastic properties. © 2011 American Chemical Society

Electrostratic stabilization of suspensions in non-aqueous media

NARCIS (Netherlands)

Hoeven, van der P.C.

1991-01-01

Concentrated suspensions of detergent powder solids in a liquid nonionic surfactant are considered for practical application as liquid detergent products. If no precautions are taken, upon storage the viscosity of such suspensions increases and the pourability drops because the suspensions are

Phase behaviour of charged colloidal sphere dispersions with added polymer chains

International Nuclear Information System (INIS)

Fortini, Andrea; Dijkstra, Marjolein; Tuinier, Remco

2005-01-01

We study the stability of mixtures of highly screened repulsive charged spheres and non-adsorbing ideal polymer chains in a common solvent using free volume theory. The effective interaction between charged colloids in an aqueous salt solution is described by a screened Coulomb pair potential, which supplements the pure hard-sphere interaction. The ideal polymer chains are treated as spheres that are excluded from the colloids by a hard-core interaction, whereas the interaction between two ideal chains is set to zero. In addition, we investigate the phase behaviour of charged colloid-polymer mixtures in computer simulations, using the two-body (Asakura-Oosawa pair potential) approximation to the effective one-component Hamiltonian of the charged colloids. Both our results obtained from simulations and from free volume theory show similar trends. We find that the screened Coulomb repulsion counteracts the effect of the effective polymer-mediated attraction. For mixtures of small polymers and relatively large charged colloidal spheres, the fluid-crystal transition shifts to significantly larger polymer concentrations with increasing range of the screened Coulomb repulsion. For relatively large polymers, the effect of the screened Coulomb repulsion is weaker. The resulting fluid-fluid binodal is only slightly shifted towards larger polymer concentrations upon increasing the range of the screened Coulomb repulsion. In conclusion, our results show that the miscibility of dispersions containing charged colloids and neutral non-adsorbing polymers increases upon increasing the range of the screened Coulomb repulsion, or upon lowering the salt concentration, especially when the polymers are small compared to the colloids

Colloids as a sink for certain pharmaceuticals in the aquatic environment.

Science.gov (United States)

Maskaoui, Khalid; Zhou, John L

2010-05-01

The occurrence and fate of pharmaceuticals in the aquatic environment is recognized as one of the emerging issues in environmental chemistry and as a matter of public concern. Existing data tend to focus on the concentrations of pharmaceuticals in the aqueous phase, with limited studies on their concentrations in particulate phase such as sediments. Furthermore, current water quality monitoring does not differentiate between soluble and colloidal phases in water samples, hindering our understanding of the bioavailability and bioaccumulation of pharmaceuticals in aquatic organisms. In this study, an investigation was conducted into the concentrations and phase association (soluble, colloidal, suspended particulate matter or SPM) of selected pharmaceuticals (propranolol, sulfamethoxazole, meberverine, thioridazine, carbamazepine, tamoxifen, indomethacine, diclofenac, and meclofenamic acid) in river water, effluents from sewage treatment works (STW), and groundwater in the UK. The occurrence and phase association of selected pharmaceuticals propranolol, sulfamethoxazole, meberverine, thioridazine, carbamazepine, tamoxifen, indomethacine, diclofenac, and meclofenamic acid in contrasting aquatic environments (river, sewage effluent, and groundwater) were studied. Colloids were isolated by cross-flow ultrafiltration (CFUF). Water samples were extracted by solid-phase extraction (SPE), while SPM was extracted by microwave. All sample extracts were analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) in the multiple reaction monitoring. Five compounds propranolol, sulfamethoxazole, carbamazepine, indomethacine, and diclofenac were detected in all samples, with carbamazepine showing the highest concentrations in all phases. The highest concentrations of these compounds were detected in STW effluents, confirming STW as a key source of these compounds in the aquatic environments. The calculation of partition coefficients of pharmaceuticals between SPM and

Stability and aggregation of nanoscale titanium dioxide particle (nTiO2): Effect of cation valence, humic acid, and clay colloids.

Science.gov (United States)

Tang, Zhong; Cheng, Tao

2018-02-01

Fate and transport of engineered nanoscale titanium dioxide (nTiO 2 ) have received much attention during the past decade. The aggregation and stability of nTiO 2 in water with complicated components, however, have not been fully examined. The objective of this paper is to determine the individual and synergistic effect of cation valence, humic acid, and clay colloids on nTiO 2 stability and aggregation, and elucidate the related mechanisms. We conducted systematic laboratory experiments to determine nTiO 2 stability and aggregation in NaCl and MgCl 2 solutions, both in the absence and presence of humic acid and illite colloids. Results showed that Mg 2+ , in comparison to Na + , could make the zeta potential of nTiO 2 more positive, and shift the point of zero charge of nTiO 2 (pH pzc,TiO2 ) towards higher pH. We also found that nTiO 2 are destabilized by illite colloids at pH < pH pzc,TiO2 through formation of illite-nTiO 2 hetero-aggregates, but are not interfered by illite colloids at higher pH. HA was found to make nTiO 2 stable via electrostatic and steric effects, both in the absence and presence of illite colloids. Calculated interaction energy based on DLVO theory revealed that instability of the nTiO 2 suspensions is mainly caused by primary minima, and that secondary minima normally do not destabilize the suspension, even though they are found to promote aggregation. Copyright © 2017 Elsevier Ltd. All rights reserved.

Experimental studies on the inventory of cement-derived colloids in the pore water of a cementitious backfill material

Energy Technology Data Exchange (ETDEWEB)

Wieland, E

2001-06-01

The potential role of near-field colloids for the colloid-facilitated migration of radionuclides has stimulated investigations concerning the generation and presence of colloids in the near-field of a repository for low- and intermediate level waste (L/ILW). The highly gas permeable mortar (Nagra designation: mortar M1) is currently favoured as backfill material for the engineered barrier of the planned Swiss L/ILW repository. The cementitious backfill is considered to be a chemical environment with some potential for colloid generation. In a series of batch-style laboratory experiments the physico-chemical processes controlling the inventory of colloids in cement pore water of the backfill were assessed for chemical conditions prevailing in the initial stage of the cement degradation. In these experiments, backfill mortar M1 or quartz, respectively, which may be used as aggregate material for the backfill, were immersed in artificial cement pore water (a NaOH/KOH rich cement fluid). Colloid concentrations in the cement pore water were recorded as a function of time for different experimental settings. The results indicate that a colloid-colloid interaction process (coagulation) controlled the colloid inventory. The mass concentration of dispersed colloids was found to be typically lower than 0.02 ppm in undisturbed batch systems. An upper-bound value was estimated to be 0.1 ppm taking into account uncertainties on the measurements. To assess the potential for colloid generation in a dynamic system, colloid concentrations were determined in the pore water of a column filled with backfill mortar. The chemical conditions established in the mortar column corresponded to conditions observed in the second stage of the cement degradation (a Ca(OH){sub 2{sup -}} controlled cement system). In this dynamic system, the upper-bound value for the colloid mass concentration was estimated to be 0.1 ppm. Implications for radionuclide mobility were deduced taking into account the

Colloidal behavior of goethite nanoparticles modified with humic acid and implications for aquifer reclamation

Energy Technology Data Exchange (ETDEWEB)

Tiraferri, Alberto; Saldarriaga Hernandez, Laura Andrea; Bianco, Carlo; Tosco, Tiziana; Sethi, Rajandrea, E-mail: rajandrea.sethi@polito.it [Politecnico di Torino, Department of Land, Environment, and Infrastructure Engineering (DIATI) (Italy)

2017-03-15

Nanosized colloids of iron oxide adsorb heavy metals, enhance the biodegradation of contaminants, and represent a promising technology to clean up contaminated aquifers. Goethite particles for aquifer reclamation were recently synthesized with a coating of humic acids to reduce aggregation. This study investigates the stability and the mobility in porous media of this material as a function of aqueous chemistry, and it identifies the best practices to maximize the efficacy of the related remediation. Humic acid-coated nanogoethite (hydrodynamic diameter ∼90 nm) displays high stability in solutions of NaCl, consistent with effective electrosteric stabilization. However, particle aggregation is fast when calcium is present and, to a lesser extent, also in the presence of magnesium. This result is rationalized with complexation phenomena related to the interaction of divalent cations with humic acid, inducing rapid flocculation and sedimentation of the suspensions. The calcium dose, i.e., the amount of calcium ions with respect to solids in the dispersion, is the parameter governing stability. Therefore, more concentrated slurries may be more stable and mobile in the subsurface than dispersions of low particle concentration. Particle concentration during field injection should be thus chosen based on concentration and proportion of divalent cations in groundwater.

Wavelength-dependent Faraday–Tyndall effect on laser-induced microbubble in gold colloid

International Nuclear Information System (INIS)

Liaw, Jiunn-Woei; Tsai, Shiao-Wen; Lin, Hung-Hsun; Yen, Tzu-Chen; Chen, Bae-Renn

2012-01-01

The cavitation microbubbles in dilute gold colloids of different concentrations (2–10 ppm) induced by a focused nanosecond-pulsed laser beam were measured and characterized at different wavelengths by using the passive and active ultrasound measurements. Three colloids with gold nanoparticles (GNPs) of different sizes (10, 45, and 75 nm) were used for experiment. The results show that the lifespan of the microbubble is reduced as the concentration of GNP increases, particularly at the wavelength of 532 nm, the surface plasmon resonance (SPR) of GNP. In contrast, at the off-resonant wavelength (e.g. 700 nm), the lifespan reduction is relatively small. This wavelength-dependent cavitation is attributed to the Faraday–Tyndall effect, a strong light scattering by GNPs. A slight defocusing of the Gaussian beam in gold colloid was proposed. Hence, the waist of the focused beam increases to reduce the optical breakdown in gold colloid. For simplicity, a linear relation between the incremental waist radius of Gaussian beam and the concentration of GNP was assumed. According to this formulation, the theoretical results are consistent with the experimental ones. In addition, the dynamics of the microbubble in gold colloid measured by the active ultrasound method agree with the Rayleigh–Plesset model. -- Highlights: ► The Faraday–Tyndall effect of gold colloid on laser induced microbubble is studied. ► Faraday–Tyndall effect of gold colloid causes the defocusing of laser beam. ► Lifespan of the microbubble is reduced as the concentration of GNP increases. ► Light scattering of laser beam at the surface plasmon resonance of GNP is the maximum.

Large scale structures in liquid crystal/clay colloids

Science.gov (United States)

van Duijneveldt, Jeroen S.; Klein, Susanne; Leach, Edward; Pizzey, Claire; Richardson, Robert M.

2005-04-01

Suspensions of three different clays in K15, a thermotropic liquid crystal, have been studied by optical microscopy and small angle x-ray scattering. The three clays were claytone AF, a surface treated natural montmorillonite, laponite RD, a synthetic hectorite, and mined sepiolite. The claytone and laponite were sterically stabilized whereas sepiolite formed a relatively stable suspension in K15 without any surface treatment. Micrographs of the different suspensions revealed that all three suspensions contained large scale structures. The nature of these aggregates was investigated using small angle x-ray scattering. For the clays with sheet-like particles, claytone and laponite, the flocs contain a mixture of stacked and single platelets. The basal spacing in the stacks was independent of particle concentration in the suspension and the phase of the solvent. The number of platelets in the stack and their percentage in the suspension varied with concentration and the aspect ratio of the platelets. The lath shaped sepiolite did not show any tendency to organize into ordered structures. Here the aggregates are networks of randomly oriented single rods.

Large scale structures in liquid crystal/clay colloids

International Nuclear Information System (INIS)

Duijneveldt, Jeroen S van; Klein, Susanne; Leach, Edward; Pizzey, Claire; Richardson, Robert M

2005-01-01

Suspensions of three different clays in K15, a thermotropic liquid crystal, have been studied by optical microscopy and small angle x-ray scattering. The three clays were claytone AF, a surface treated natural montmorillonite, laponite RD, a synthetic hectorite, and mined sepiolite. The claytone and laponite were sterically stabilized whereas sepiolite formed a relatively stable suspension in K15 without any surface treatment. Micrographs of the different suspensions revealed that all three suspensions contained large scale structures. The nature of these aggregates was investigated using small angle x-ray scattering. For the clays with sheet-like particles, claytone and laponite, the flocs contain a mixture of stacked and single platelets. The basal spacing in the stacks was independent of particle concentration in the suspension and the phase of the solvent. The number of platelets in the stack and their percentage in the suspension varied with concentration and the aspect ratio of the platelets. The lath shaped sepiolite did not show any tendency to organize into ordered structures. Here the aggregates are networks of randomly oriented single rods

Magneto-optical characterization of colloidal dispersions. Application to nickel nanoparticles.

Science.gov (United States)

Pascu, Oana; Caicedo, José Manuel; Fontcuberta, Josep; Herranz, Gervasi; Roig, Anna

2010-08-03

We report here on a fast magneto-optical characterization method for colloidal liquid dispersions of magnetic nanoparticles. We have applied our methodology to Ni nanoparticles with size equal or below 15 nm synthesized by a ligand stabilized solution-phase synthesis. We have measured the magnetic circular dichroism (MCD) of colloidal dispersions and found that we can probe the intrinsic magnetic properties within a wide concentration range, from 10(-5) up to 10(-2) M, with sensitivity to concentrations below 1 microg/mL of magnetic Ni particles. We found that the measured MCD signal scales up with the concentration thus providing a means of determining the concentration values of highly diluted dispersions. The methodology presented here exhibits large flexibility and versatility and might be suitable to study either fundamental problems related to properties of nanosize particles including surface related effects which are highly relevant for magnetic colloids in biomedical applications or to be applied to in situ testing and integration in production lines.

Synthesis of aqueous suspensions of magnetic nanoparticles with the co-precipitation of iron ions in the presence of aspartic acid

Science.gov (United States)

Pušnik, Klementina; Goršak, Tanja; Drofenik, Miha; Makovec, Darko

2016-09-01

There is increasing demand for the production of large quantities of aqueous suspensions of magnetic iron-oxide nanoparticles. Amino acids are one possible type of inexpensive, nontoxic, and biocompatible molecules that can be used as the surfactants for the preparation of stable suspensions. This preparation can be conducted in a simple, one-step process based on the co-precipitation of Fe3+/Fe2+ ions in the presence of the amino acid. However, the presence of this amino acid changes the mechanism of the magnetic nanoparticles' formation. In this investigation we analyzed the influence of aspartic amino acid (Asp) on the formation of magnetic iron-oxide nanoparticles during the co-precipitation. The process of the nanoparticles' formation was followed using a combination of TEM, x-ray diffractometry, magnetic measurements, in-situ FT-IR spectroscopy, and chemical analysis, and compared with the formation of nanoparticles without the Asp. The Asp forms a coordination complex with the Fe3+ ions, which impedes the formation of the intermediate iron oxyhydroxide phase and suppresses the growth of the final magnetic iron-oxide nanoparticles. Slower reaction kinetics can lead to the formation of nonmagnetic secondary phases. The aspartic-acid-absorbed nanoparticles can be dispersed to form relatively concentrated aqueous suspensions displaying a good colloidal stability at an increased pH.

Phosphate Suspension Chromium (III) radiolabelled with 32P and 90Y

International Nuclear Information System (INIS)

Cruz Arencibia, Jorge; Turiño Pérez, David; Cruz Morales, Amed; Morín Zorrilla, José; Taylor Delgado, Tamara; García Rodríguez, Enrique; Baganet Cobas, Aymara

2016-01-01

Chronic synovitis is a manifestation common joint of rheumatoid arthritis, hemophilia and other systemic diseases. The modalities of treatment of this complication radiosynoviorthesis stands out for its good response, ease of implementation and lower total cost. In the United States, Europe and some countries in Latin America they are used to this different radioactive colloids and suspensions. In Cuba it was developed and is approved suspension Chromic Phosphate 32 P-labeled. At work the consistency of the production process of this suspension is examined. As a result of the evaluation was found that the suspension is characterized by a radiochemical purity of 94 ± 1% and particle size predominantly of 91 ± 3 between 0.2-10 microns. The results achieved in regular production and application to patients with rheumatic diseases and hemophiliacs, with follow-up to one year prove their efficacy and safety, the latter associated with low leakage articular detected and the absence of adverse reactions. Also at work the results achieved in the development of a technology for the production of suspension Phosphate Chromium (III) labeled with 90 Y, similarly to existing 32 P composition is exposed, and properties even more favorable, in particular radiochemical purity of 97%, favoring the registration of a radiopharmaceutical with better technical and economic characteristics, which must ensures the use of this form of treatment in the country. (author)

Prediction of Nanoparticle and Colloid Attachment on Unfavorable Mineral Surfaces Using Representative Discrete Heterogeneity.

Science.gov (United States)

Trauscht, Jacob; Pazmino, Eddy; Johnson, William P

2015-09-01

Despite several decades of research there currently exists no mechanistic theory to predict colloid attachment in porous media under environmental conditions where colloid-collector repulsion exists (unfavorable conditions for attachment). It has long been inferred that nano- to microscale surface heterogeneity (herein called discrete heterogeneity) drives colloid attachment under unfavorable conditions. Incorporating discrete heterogeneity into colloid-collector interaction calculations in particle trajectory simulations predicts colloid attachment under unfavorable conditions. As yet, discrete heterogeneity cannot be independently measured by spectroscopic or other approaches in ways directly relevant to colloid-surface interaction. This, combined with the fact that a given discrete heterogeneity representation will interact differently with differently sized colloids as well as different ionic strengths for a given sized colloid, suggests a strategy to back out representative discrete heterogeneity by a comparison of simulations to experiments performed across a range of colloid size, solution IS, and fluid velocity. This has recently been performed for interaction of carboxylate-modified polystyrene latex (CML) microsphere attachment to soda lime glass at pH 6.7 with NaCl electrolyte. However, extension to other surfaces, pH values, and electrolytes is needed. For this reason, the attachment of CML (0.25, 1.1, and 2.0 μm diameters) from aqueous suspension onto a variety of unfavorable mineral surfaces (soda lime glass, muscovite, and albite) was examined for pH values of 6.7 and 8.0), fluid velocities (1.71 × 10(-3) and 5.94 × 10(-3) m s(-1)), IS (6.0 and 20 mM), and electrolytes (NaCl, CaSO4, and multivalent mixtures). The resulting representative heterogeneities (heterodomain size and surface coverage, where heterodomain refers to nano- to microscale attractive domains) yielded colloid attachment predictions that were compared to predictions from existing

Colloids or artefacts? A TVO/SKB cooperation project in Olkiluoto, Finland

International Nuclear Information System (INIS)

Laaksoharju, M.; Vuorinen, U.; Snellman, M.; Helenius, J.; Allard, B.; Pettersson, C.; Hinkkanen, H.

1993-12-01

TVO (Teollisuuden Voima Oy, Finland) initiated a co-operative task with SKB (Swedish Nuclear Fuel and Waste Management Co.) to critically evaluate colloid sampling methods at the test site in Olkiluoto, SW Finland. Three different colloid sampling methods were compared when sampling borehole OL-KR1 at 613-618 m depth. One possible way to make a conservative in-situ colloid estimation is to omit the contribution from calcite precipitation which is considered to be the main artefact. When this is made the inorganic colloid content (size 1-1000 nm) in Olkiluoto is 184 ±177 ppb consisting of clay minerals, silica, pyrite, goethite and magnesium oxide; the concentration of organic substances are around 100 ppb. The in-situ colloid concentration seems to be low which is in good agreement with experiences from years of sampling in similar environment and depths. The exercise shows the many difficulties encountered when sampling colloids. Small error in the planning, pump rate selection, a lack of precautionary measures, artefact sensitivity of the method etc have a tendency to affect significantly the results on the measured ppb colliod level

On the aging and colloid properties of AgI soils

International Nuclear Information System (INIS)

Despotovicj, R.; Kapetanovicj, J.

1977-01-01

A study of the changes of silver iodide sol properties has shown the role of the ageing process in the characterization of the colloid system. An analysis of the critical coagulation concentration changes and of the sedimentation rates with time and electrophoretic mobility of sols has revealed, that sols in the presence of various counter ions do not exhibit strictly equal colloid properties, although counter ions are present at the critical coagulation concentration

Colloidal silica films for high-capacity DNA arrays

Science.gov (United States)

Glazer, Marc Irving

The human genome project has greatly expanded the amount of genetic information available to researchers, but before this vast new source of data can be fully utilized, techniques for rapid, large-scale analysis of DNA and RNA must continue to develop. DNA arrays have emerged as a powerful new technology for analyzing genomic samples in a highly parallel format. The detection sensitivity of these arrays is dependent on the quantity and density of immobilized probe molecules. We have investigated substrates with a porous, "three-dimensional" surface layer as a means of increasing the surface area available for the synthesis of oligonucleotide probes, thereby increasing the number of available probes and the amount of detectable bound target. Porous colloidal silica films were created by two techniques. In the first approach, films were deposited by spin-coating silica colloid suspensions onto flat glass substrates, with the pores being formed by the natural voids between the solid particles (typically 23nm pores, 35% porosity). In the second approach, latex particles were co-deposited with the silica and then pyrolyzed, creating films with larger pores (36 nm), higher porosity (65%), and higher surface area. For 0.3 mum films, enhancements of eight to ten-fold and 12- to 14-fold were achieved with the pure silica films and the films "templated" with polymer latex, respectively. In gene expression assays for up to 7,000 genes using complex biological samples, the high-capacity films provided enhanced signals and performed equivalently or better than planar glass on all other functional measures, confirming that colloidal silica films are a promising platform for high-capacity DNA arrays. We have also investigated the kinetics of hybridization on planar glass and high-capacity substrates. Adsorption on planar arrays is similar to ideal Langmuir-type adsorption, although with an "overshoot" at high solution concentration. Hybridization on high-capacity films is

Colloid characterization and in situ release in shallow groundwater under different hydrogeology conditions.

Science.gov (United States)

Zhou, Jingjing; Liu, Dan; Zhang, Wenjing; Chen, Xuequn; Huan, Ying; Yu, Xipeng

2017-06-01

Changes to groundwater hydrodynamics and chemistry can lead to colloid release that can have a major impact on the groundwater environment. To analyze the effects of colloid release caused by artificial groundwater recharge, field and laboratory tests on colloid characterization and colloid release were conducted. The field tests were carried out at an artificial recharge test site in Shandong Province. In the field investigation, one recharge water sample and five groundwater samples were collected and filtered through three levels of ultrafiltration membranes, with pore sizes of 0.45 μm, 100 kDa, and 50 kDa. The field results indicated that the colloid mass concentrations in groundwater retained between membranes with pore sizes of 100 kDa-0.45 μm and 50 kDa-100 kDa were 19 and 62 mg/L, respectively. In recharge water, the colloid mass concentrations retained by 100-kDa-0.45-μm and 50-kDa-100-kDa membranes were 3 and 99 mg/L, respectively. Colloids detected on the ultrafiltration membranes were mainly inorganic between 100 kDa and 0.45 μm, and mainly organic between 50 and 100 kDa. Based on the field colloid investigation results, the organic colloid was chosen in the laboratory experiments to reveal its release behavior under different conditions. Porous media diameter, flux, ionic strength (IS), and ion valence were changed to determine their influences on organic colloid concentration outflow from undisturbed porous media. The experiment's results indicate that decreasing the diameter, and increasing the flux, ionic strength, and the number of divalent cations, can promote organic colloid release. The organic colloid release rate in the early stage was high and is thus likely to affect the quality of groundwater. The results provide a useful scientific basis for minimizing changes to hydrodynamic and hydrochemical conditions during artificial recharge, thus safeguarding groundwater quality.

Zein nanoparticles and the strategies to improve the colloidal stability: a mini review

Science.gov (United States)

Pascoli, Mônica; de Lima, Renata; Fraceto, Leonardo F.

2018-01-01

Zein, a protein extracted from maize, can be employed to easily produce nanoscale particles suitable for use as carrier systems. This review investigates the main methods for obtaining zein nanoparticles, as well as the problems and options available in the development of stable colloidal suspensions. Considerable gaps were identified in the literature concerning this topic, with studies being unclear about the factors that affect the stability of zein particles. In the vast majority of cases, no data are presented in relation to the stability of the formulations over time. It could be concluded that in order to produce a high quality system, detailed evaluation is required, considering factors including the zein concentration, pH, ionic strength, thermal treatment of the protein prior to preparation of the nanoparticles, strategies employing other materials as coatings, and the storage conditions. It is extremely important that these aspects should be considered during product development, prior to commercial-scale manufacture.

Solution or suspension - Does it matter for lipid based systems? In vivo studies of chase dosing lipid vehicles with aqueous suspensions of a poorly soluble drug.

Science.gov (United States)

Larsen, A T; Holm, R; Müllertz, A

2017-08-01

In this study, the potential of co-administering an aqueous suspension with a placebo lipid vehicle, i.e. chase dosing, was investigated in rats relative to the aqueous suspension alone or a solution of the drug in the lipid vehicle. The lipid investigated in the present study was Labrafil M2125CS and three evaluated poorly soluble model compounds, danazol, cinnarizine and halofantrine. For cinnarizine and danazol the oral bioavailability in rats after chase dosing or dosing the compound dissolved in Labrafil M21515CS was similar and significantly higher than for the aqueous suspension. For halofantrine the chase dosed group had a tendency towards a low bioavailability relative to the Labrafil M2125CS solution, but still a significant higher bioavailability relative to the aqueous suspension. This could be due to factors such as a slower dissolution rate in the intestinal phase of halofantrine or a lower solubility in the colloidal structures formed during digestion, but other mechanisms may also be involved. The study thereby supported the potential of chase dosing as a potential dosing regimen in situations where it is beneficial to have a drug in the solid state, e.g. due to chemical stability issues in the lipid vehicle. Copyright © 2017 Elsevier B.V. All rights reserved.

Non-homogeneous flow profiles in sheared bacterial suspensions

Science.gov (United States)

Samanta, Devranjan; Cheng, Xiang

Bacterial suspensions under shear exhibit interesting rheological behaviors including the remarkable ``superfluidic'' state with vanishing viscosity at low shear rates. Theoretical studies have shown that such ``superfluidic'' state is linked with non-homogeneous shear flows, which are induced by coupling between nematic order of active fluids and hydrodynamics of shear flows. However, although bulk rheology of bacterial suspensions has been experimentally studied, shear profiles within bacterial suspensions have not been explored so far. Here, we experimentally investigate the flow behaviors of E. coli suspensions under planar oscillatory shear. Using confocal microscopy and PIV, we measure velocity profiles across gap between two shear plates. We find that with increasing shear rates, high-concentration bacterial suspensions exhibit an array of non-homogeneous flow behaviors like yield-stress flows and shear banding. We show that these non-homogeneous flows are due to collective motion of bacterial suspensions. The phase diagram of sheared bacterial suspensions is systematically mapped as functions of shear rates an bacterial concentrations. Our experiments provide new insights into rheology of bacterial suspensions and shed light on shear induced dynamics of active fluids. Chemical Engineering and Material Science department.

Large-scale assembly of colloidal particles

Science.gov (United States)

Yang, Hongta

This study reports a simple, roll-to-roll compatible coating technology for producing three-dimensional highly ordered colloidal crystal-polymer composites, colloidal crystals, and macroporous polymer membranes. A vertically beveled doctor blade is utilized to shear align silica microsphere-monomer suspensions to form large-area composites in a single step. The polymer matrix and the silica microspheres can be selectively removed to create colloidal crystals and self-standing macroporous polymer membranes. The thickness of the shear-aligned crystal is correlated with the viscosity of the colloidal suspension and the coating speed, and the correlations can be qualitatively explained by adapting the mechanisms developed for conventional doctor blade coating. Five important research topics related to the application of large-scale three-dimensional highly ordered macroporous films by doctor blade coating are covered in this study. The first topic describes the invention in large area and low cost color reflective displays. This invention is inspired by the heat pipe technology. The self-standing macroporous polymer films exhibit brilliant colors which originate from the Bragg diffractive of visible light form the three-dimensional highly ordered air cavities. The colors can be easily changed by tuning the size of the air cavities to cover the whole visible spectrum. When the air cavities are filled with a solvent which has the same refractive index as that of the polymer, the macroporous polymer films become completely transparent due to the index matching. When the solvent trapped in the cavities is evaporated by in-situ heating, the sample color changes back to brilliant color. This process is highly reversible and reproducible for thousands of cycles. The second topic reports the achievement of rapid and reversible vapor detection by using 3-D macroporous photonic crystals. Capillary condensation of a condensable vapor in the interconnected macropores leads to the

Evaluation of sup(99m)Tc-Sn-colloid on liver scintigram

Energy Technology Data Exchange (ETDEWEB)

Matsuyuki, Y; Kanao, K; Honda, M; Ishihara, S [Sumitomo Hospital, Osaka (Japan)

1975-04-01

sup(99m)Tc-Sn-colloid injectable solution and Sn-colloid preparation set were used for nuclear medical examination of the liver and their efficiency was discussed. Both sup(99m)Tc-Sn-colloid injectable solution and Sn-colloid preparation set showed the same kinetics in vivo, and the sup(99m)Tc-Sn-colloid rapidly disappeared from the serum and concentrated to the liver and spleen. Comparing /sup 198/Au-colloid, sup(99m)Tc-Sn-colloid could be increased the administration dose, and provided easy examination within short time period, easy observation from multiple directions, and improvement of resolution by scinticamera. Imaging of the spleen with sup(99m)Tc-Sn-colloid was slightly superior to that with sup(99m)Tc-sulfur-colloid. sup(99m)Tc-Sn-colloid injectable solution which required no procedure of labeling was evaluated as the most safe and easy technique. Side effects were not recognized. As the results, already made preparation, such as sup(99m)Tc-Sn-colloid injectable solution, which provided easy preparation with less absorbed dose of the tissue and high resolution would be frequently required.

Evaluation of sup(99m)Tc-Sn-colloid on liver scintigram

International Nuclear Information System (INIS)

Matsuyuki, Yoshihiko; Kanao, Keisuke; Honda, Minoru; Ishihara, Shizumori

1975-01-01

sup(99m)Tc-Sn-colloid injectable solution and Sn-colloid preparation set were used for nuclear medical examination of the liver and their efficiency was discussed. Both sup(99m)Tc-Sn-colloid injectable solution and Sn-colloid preparation set showed the same kinetics in vivo, and the sup(99m)Tc-Sn-colloid rapidly disappeared from the serum and concentrated to the liver and spleen. Comparing 198 Au-colloid, sup(99m)Tc-Sn-colloid could be increased the administration dose, and provided easy examination within short time period, easy observation from multiple directions, and improvement of resolution by scinticamera. Imaging of the spleen with sup(99m)Tc-Sn-colloid was slightly superior to that with sup(99m)Tc-sulfur-colloid. sup(99m)Tc-Sn-colloid injectable solution which required no procedure of labeling was evaluated as the most safe and easy technique. Side effects were not recognized. As the results, already made preparation, such as sup(99m)Tc-Sn-colloid injectable solution, which provided easy preparation with less absorbed dose of the tissue and high resolution would be frequently required. (Mukohata, S.)

Electro-elastoviscous response of polyaniline functionalized nano-porous zeolite based colloidal dispersions.

Science.gov (United States)

Chattopadhyay, Ankur; Rani, Poonam; Srivastava, Rajendra; Dhar, Purbarun

2018-06-01

The present article discusses the typical influence of grafted conducting polymers in the mesoscale pores of dielectric particles on the static and dynamic electrorheology and electro-viscoelastic behavior of corresponding colloids. Nanocrystalline meso-nanoporous zeolite has been prepared by chemical synthesis and subsequently polyaniline (PANI) coating has been implemented. Electrorheological (ER) suspensions have been formed by dispersing the nanoparticles in silicone oil and their viscoelastic behaviors are examined to understand the nature of such complex colloidal systems under electric fields. PANI-Zeolite ER fluids demonstrate higher static electroviscous effects and yield stress potential than untreated Zeolite, typically studied in literature. Transient electro-viscous characterizations show a stable and negligible hysteresis behavior when both the fluids are exposed to constant as well as time varying electric field intensities. Further oscillatory shear experiments of frequency and strain sweeps exhibit predominant elastic behavior in case of Zeolite based ER suspensions as compared to PANI systems. Detailed investigations reveal Zeolite based ER suspensions display enhanced relative yielding as well as electro-viscoelastic stability than the PANI-Zeolite. The steady state viscous behaviors are scaled against the non-dimensional Mason number to model the system behavior for both fluids. Experimental data of flow behaviors of both the ER fluids are compared with semi-classical models and it is found that the CCJ model possesses a closer proximity than traditional Bingham model, thereby revealing the fluids to be generic pseudo-linear fluids. The present article reveals that while the PANI based fluids are typically hailed superior in literature, it is only restricted to steady shear utilities. In case of dynamic and oscillatory systems, the traditional Zeolite based fluids exhibit superior ER caliber. Copyright © 2018 Elsevier Inc. All rights reserved.

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

Science.gov (United States)

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.

Colloidal silver solutions with antimicrobial properties

International Nuclear Information System (INIS)

Petica, A.; Gavriliu, S.; Lungu, M.; Buruntea, N.; Panzaru, C.

2008-01-01

Some colloidal silver solutions involving the electrochemical technique with 'sacrificial anode method and different stabilizers and co-stabilizers' have been prepared. A constant current pulse generator with stirrer at different working times has been used. To achieve stable colloidal silver solutions, a mix of different tensioactive agents namely [poly (N-vinylpyrrolidone)], Na-naphthalene sulphonate, Na-lauryl sulfate and Na-dodecyl sulphonate were tested. The effects of these various mixes of polymer and ionic surfactants upon the Ag concentration and UV-vis spectra of silver nanoparticles were determined by spectrophotometer techniques. The nanoparticles sizes have been analyzed through dynamic light scattering technique and the silver nanoparticle morphology has been evidenced by transmission electron microscopy (TEM). Micobiological analysis has been made by determining minimal inhibitorial concentration upon the following germs: Staphylococcus aureus (ATCC) (Gram-positive cocci), Pseudomonas aeruginosa (ATTC), Escherichia coli (ATCC) and Acinetobacter spp. (Gram-negative coccobacillus). To evaluate the antifungal effect, the antibiogram method involving various tests using a fungi mix of Aspergillus, Penicillium and Trichoderma species has been used. The presented method allows obtaining of some stable colloidal solutions containing up to 35 ppm of Ag with very good antimicrobial and antifungal properties

Colloidal silver solutions with antimicrobial properties

Energy Technology Data Exchange (ETDEWEB)

Petica, A. [INCDIE ICPE-Advanced Research, Bucharest (Romania)], E-mail: petica@icpe-ca.ro; Gavriliu, S.; Lungu, M.; Buruntea, N. [INCDIE ICPE-Advanced Research, Bucharest (Romania); Panzaru, C. [Institute of Medicine and Pharmacy, Iassy (Romania)

2008-08-25

Some colloidal silver solutions involving the electrochemical technique with 'sacrificial anode method and different stabilizers and co-stabilizers' have been prepared. A constant current pulse generator with stirrer at different working times has been used. To achieve stable colloidal silver solutions, a mix of different tensioactive agents namely [poly (N-vinylpyrrolidone)], Na-naphthalene sulphonate, Na-lauryl sulfate and Na-dodecyl sulphonate were tested. The effects of these various mixes of polymer and ionic surfactants upon the Ag concentration and UV-vis spectra of silver nanoparticles were determined by spectrophotometer techniques. The nanoparticles sizes have been analyzed through dynamic light scattering technique and the silver nanoparticle morphology has been evidenced by transmission electron microscopy (TEM). Micobiological analysis has been made by determining minimal inhibitorial concentration upon the following germs: Staphylococcus aureus (ATCC) (Gram-positive cocci), Pseudomonas aeruginosa (ATTC), Escherichia coli (ATCC) and Acinetobacter spp. (Gram-negative coccobacillus). To evaluate the antifungal effect, the antibiogram method involving various tests using a fungi mix of Aspergillus, Penicillium and Trichoderma species has been used. The presented method allows obtaining of some stable colloidal solutions containing up to 35 ppm of Ag with very good antimicrobial and antifungal properties.

Non-Newtonian flow between concentric cylinders calculated from thermophysical properties obtained from simulations

International Nuclear Information System (INIS)

Narayan, A.P.; Rainwater, J.C.; Hanley, H.J.M.

1995-01-01

A study of the Weissenberg effect (rod climbing in a stirred system) based on nonequilibrium molecular dynamics (NEMD) is reported. Simulation results from a soft-sphere fluid are used to obtain a self-consistent free-surface profile of the fluid of finite compressibility undergoing Couette flow between concentric cylinders. A numerical procedure is then applied to calculate the height profile for a hypothetical fluid with thermophysical properties of the soft-sphere liquid and of a dense colloidal suspension. The height profile calculated is identified with shear thickening and the forms of the viscometric functions. The maximum climb occurs between the cylinders rather than at the inner cylinder

Shear thickening in suspensions: the lubricated-to-frictional contact scenario

Science.gov (United States)

Morris, Jeffrey

2017-11-01

Suspensions of solid particles in viscous liquids can vary from low-viscosity liquids to wet granular materials or soft solids depending on the solids loading and the forces acting between particles. When the particles are very concentrated, these mixtures are ''dense suspensions.'' Dense suspensions often exhibit shear thickening, an increase in apparent viscosity as the shear rate is increased. In its most extreme form, order of magnitude increases in viscosity over such a narrow range in shear rate occur that the term discontinuous shear thickening (DST) is applied. DST is particularly striking as it occurs in the relatively simple case of nearly hard spheres in a Newtonian liquid, and is found to take place for submicron particles in colloidal dispersions to much larger particle corn starch dispersions. We focus on simulations of a recently developed ``lubricated-to-frictional'' rheology in which the interplay of viscous lubrication, repulsive surface forces, and contact friction between particle surfaces provides a scenario to explain DST. Our simulation method brings together elements of the discrete-element method from granular flow with a simplified Stokesian Dynamics, and can rationalize not only the abrupt change in properties with imposed shear rate (or shear stress), but also the magnitude of the change. The large change in properties is associated with the breakdown of lubricating films between particles, with activation of Coulomb friction between particles. The rate dependence is caused by the shearing forces driving particles to contact, overwhelming conservative repulsive forces between surfaces; the repulsive forces are representative of colloidal stabilization by surface charge or steric effects, e.g. due to adsorbed polymer. The results of simulation are compared to developments by other groups, including a number of experimental studies and a theory incorporating the same basic elements as the simulation. The comparison to experiments of the

Naratriptan hydrochloride in extemporaneosly compounded oral suspensions.

Science.gov (United States)

Zhang, Y P; Trissel, L A; Fox, J L

2000-01-01

The purpose of this study was to determine the pharmaceutical acceptability and chemical stability of naratriptan hydrochloride in three extemporaneously compounded suspension formulations. The naratriptan-hydrochloride oral suspensions were prepared from 2.5-mg commercial tablets yielding a nominal naratriptan concentration of 0.5 mg/mL. The suspension vehicles selected for testing were Syrpalta, an equal-parts mixture of Ora-Plus and Ora-Sweet, and an equal-parts mixture of Ora-Plus and Ora-Sweet SF. The tablets were crushed and thoroughly triturated to a fine powder using a porcelain mortar and pestle. The powder was incorporated into a portion of the Syrpalta or Ora-Plus suspension vehicle and mixed until homogeneous. The mixtures were then brought to volume with Syrpalta, Ora-Sweet or Ora-Sweet SF, as appropriate. The suspensions were packaged in amber, plastic, screw-cap prescription bottles and stored at 23 deg C for seven days and 4 deg C for 90 days. An adequate suspension was never achieved in Syrpalta. The crushed-tablet powder did not produce a uniformly dispersed mixture and exhibited clumping and a high rate of sedimentation. A distinct layer of the solid tablet material settled immediately after shaking. Over the next four hours, a densely packed, yellow, caked layer formed at the bottom of the containers, making resuspension difficult. During storage, the caking became worse. Chemical analysis was not performed. The Ora-Plus and Ora-Sweet or Ora-Sweet SF suspensions had a slight greenish cast and were resuspended without difficulty by shaking for approximately ten seconds, yielding easily poured and homogeneous mixtures throughout the study. Visible settling and layering did not begin for four hours with the Ora-Sweet suspension and 24 hours for the Ora-Sweet SF suspension. High pressure liquid chromatographic analysis found that the naratriptan concentration in both suspension-vehicle combinations exhibited little or no loss for seven days at 23

Impact of colloids on uranium transport in groundwater applied to the Aube radioactive waste disposal

International Nuclear Information System (INIS)

Le Cointe, Pierre

2011-01-01

The presence of colloids, known vectors of radionuclides and chemical contaminants in groundwater, has been identified in groundwater at the Aube radioactive waste disposal in 2004. This thesis aims to characterize these colloids, and to determine their potential impact in the transport of Uranium, chosen as the element of interest for this study. The identified 60 nm in diameter clay colloids and the fulvic and humic acids can move in Aptian groundwater, as indirectly evidenced by column experiments. A feasibility study of a in situ test has been done through a transport modeling to confirm the colloid mobility at the field scale. Using the conditions of the study, the clay colloids do not influence Uranium transport. Even with the greatest concentration assumed on site, they have a very limited impact on the mobilization of Uranium, in the pH range measured on site. On the contrary, the organic colloids, despite their low concentration, can facilitate Uranium transport, the uranyl - organic acid chemical bond being exceptionally strong. Therefore their low concentration in groundwater makes their impact on uranium mobility equally insignificant. (author)

Sorption of prioritized elements on montmorillonite colloids and their potential to transport radionuclides

International Nuclear Information System (INIS)

Wold, Susanna

2010-04-01

Due to colloids potential to bind radionuclides (RN) and even mobilise sorbed RN, colloid transport of RN should be taken into account when modeling radionuclide transport in the scenario of a leaking canister in a deep bedrock repository of spent nuclear fuel. Colloids are always present in natural waters and the concentrations are controlled by the groundwater chemistry where specifically the ionic strength is of major importance. In many deep bedrock groundwaters, the ionic strength is fairly high (above the Critical Coagulation Concentration) and therefore colloids are not likely to be stable. In these types of groundwaters colloid concentrations up to 100 μg/l could be expected, and clay colloids organic degradation products and bacteria and viruses represent can be found. In a long time perspective cycles of glaciations can be expected in Sweden as in other Nordic countries. It can not be excluded that glacial melt water can intrude to repository depth with high flows. In this scenario the groundwater conditions may drastically change. In contact with dilute groundwater the bentonite barrier can start to propagate a bentonite gel and further release montmorillonite colloids into water bearing fractures. The concentration of colloids in vicinity of the bentonite barrier can then increase drastically. In contact with Grimsel groundwater types with [Na] and [Ca] of 0.001 and 0.0001 M respectively a montmorillonite concentration of a maximum of 20 mg/l is expected. Further, the groundwater chemistry of Grimsel seems to be representative for glacial meltwater when comparing with the water chemistry data on meltwaters from existing glaciers. A key to be able to model colloid transport of radionuclides is the sorption strength and the sorption reversibility. To facilitate this, a compilation of literature K d -values and an inventory of available sorption kinetic data has been composed for the prioritized elements Pu, Th, Am, Pb, Pa, Ra, Np, Cm, Ac, Tc, Cs, Nb, Ni

Sorption of prioritized elements on montmorillonite colloids and their potential to transport radionuclides

Energy Technology Data Exchange (ETDEWEB)

Wold, Susanna (Royal Inst. of Technology, Stockholm (Sweden). School of Chemical Science and Engineering, Nuclear Chemistry)

2010-04-15

Due to colloids potential to bind radionuclides (RN) and even mobilise sorbed RN, colloid transport of RN should be taken into account when modeling radionuclide transport in the scenario of a leaking canister in a deep bedrock repository of spent nuclear fuel. Colloids are always present in natural waters and the concentrations are controlled by the groundwater chemistry where specifically the ionic strength is of major importance. In many deep bedrock groundwaters, the ionic strength is fairly high (above the Critical Coagulation Concentration) and therefore colloids are not likely to be stable. In these types of groundwaters colloid concentrations up to 100 mug/l could be expected, and clay colloids organic degradation products and bacteria and viruses represent can be found. In a long time perspective cycles of glaciations can be expected in Sweden as in other Nordic countries. It can not be excluded that glacial melt water can intrude to repository depth with high flows. In this scenario the groundwater conditions may drastically change. In contact with dilute groundwater the bentonite barrier can start to propagate a bentonite gel and further release montmorillonite colloids into water bearing fractures. The concentration of colloids in vicinity of the bentonite barrier can then increase drastically. In contact with Grimsel groundwater types with [Na] and [Ca] of 0.001 and 0.0001 M respectively a montmorillonite concentration of a maximum of 20 mg/l is expected. Further, the groundwater chemistry of Grimsel seems to be representative for glacial meltwater when comparing with the water chemistry data on meltwaters from existing glaciers. A key to be able to model colloid transport of radionuclides is the sorption strength and the sorption reversibility. To facilitate this, a compilation of literature K{sub d}-values and an inventory of available sorption kinetic data has been composed for the prioritized elements Pu, Th, Am, Pb, Pa, Ra, Np, Cm, Ac, Tc, Cs, Nb

Sorption of 241Am onto montmorillonite, illite and hematite colloids

International Nuclear Information System (INIS)

Degueldre, C.; Ulrich, H.J.; Silby, H.

1994-01-01

Actinide sorption on colloids may be described as a competition between the formation of complexes in solution and the build up of surface complexes. The role of particle and of carbonate concentrations on the sorption/desorption of 241 Am on montmorillonite, illite and hematite colloids is investigated. Since the partition coefficient (K p ) values are virtually independent of the colloid concentrations, within the range 1 to 300 ppm, no significant aggregation takes place in the sorption/desorption experiment. At pH 8, a slight decrease of K p is observed if the concentration of total carbonate exceeds 10 -2 M. The formation of the carbonato- (and hydroxo-carbonato-) complexes in the solution competes with the formation of surface complexes on the colloids. A relationship between the sorption coefficient and the complexation of 241 Am in the solution has been found. This leads to the conclusion that, besides free americium cation, the hydroxo-, and carbonato- as well as the mixed hydroxo-carbonato-complexes are sorbed. Only when the tricarbonatocomplex [Am(CO 3 ) 3 ] 3- prevails (total carbonate concentration > 10 -2 M), a significant decrease of the distribution coefficient is observed. At pH 10 this decrease disappears because under these conditions the strong hydroxo-complexes dominate. A pragmatic and relatively simple application of surface complexation model describes the observed features. (orig.)

Out-of-equilibrium processes in suspensions of oppositely charged colloids: liquid-to-crystal nucleation and gel formation

Science.gov (United States)

Sanz, Eduardo

2009-03-01

We study the kinetics of the liquid-to-crystal transformation and of gel formation in colloidal suspensions of oppositely charged particles. We analyse, by means of both computer simulations and experiments, the evolution of a fluid quenched to a state point of the phase diagram where the most stable state is either a homogeneous crystalline solid or a solid phase in contact with a dilute gas. On the one hand, at high temperatures and high packing fractions, close to an ordered-solid/disordered-solid coexistence line, we find that the fluid-to-crystal pathway does not follow the minimum free energy route. On the other hand, a quench to a state point far from the ordered-crystal/disordered-crystal coexistence border is followed by a fluid-to-solid transition through the minimum free energy pathway. At low temperatures and packing fractions we observe that the system undergoes a gas-liquid spinodal decomposition that, at some point, arrests giving rise to a gel-like structure. Both our simulations and experiments suggest that increasing the interaction range favors crystallization over vitrification in gel-like structures. [4pt] In collaboration with Chantal Valeriani, Soft Condensed Matter, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, 3584 CC Utrecht, The Netherlands and SUPA, School of Physics, University of Edinburgh, JCMB King's Buildings, Mayfield Road, Edinburgh EH9 3JZ, UK; Teun Vissers, Andrea Fortini, Mirjam E. Leunissen, and Alfons van Blaaderen, Soft Condensed Matter, Debye Institute for Nanomaterials Science, Utrecht University; Daan Frenke, FOM Institute for Atomic and Molecular Physics, Kruislaan 407, 1098 SJ Amsterdam, The Netherlands and Department of Chemistry, University of Cambridge, Lensfield Road, CB2 1EW, Cambridge, UK; and Marjolein Dijkstra, Soft Condensed Matter, Debye Institute for Nanomaterials Science, Utrecht University.

Iron colloids reduce the bioavailability of phosphorus to the green alga Raphidocelis subcapitata.

Science.gov (United States)

Baken, Stijn; Nawara, Sophie; Van Moorleghem, Christoff; Smolders, Erik

2014-08-01

Phosphorus (P) is a limiting nutrient in many aquatic systems. The bioavailability of P in natural waters strongly depends on its speciation. In this study, structural properties of iron colloids were determined and related to their effect on P sorption and P bioavailability. The freshwater green alga Raphidocelis subcapitata was exposed to media spiked with radiolabelled (33)PO4, and the uptake of (33)P was monitored for 1 h. The media contained various concentrations of synthetic iron colloids with a size between 10 kDa and 0.45 μm. The iron colloids were stabilised by natural organic matter. EXAFS spectroscopy showed that these colloids predominantly consisted of ferrihydrite with small amounts of organically complexed Fe. In colloid-free treatments, the P uptake flux by the algae obeyed Michaelis-Menten kinetics. In the presence of iron colloids at 9 or 90 μM Fe, corresponding to molar P:Fe ratios between 0.02 and 0.17, the truly dissolved P (<10 kDa) was between 4 and 60% of the total dissolved P (<0.45 μm). These colloids reduced the P uptake flux by R. subcapitata compared to colloid-free treatments at the same total dissolved P concentration. However, the P uptake flux from colloid containing solutions equalled that from colloid-free ones when expressed as truly dissolved P. This demonstrates that colloidal P did not contribute to the P uptake flux. It is concluded that, on the short term, phosphate adsorbed to ferrihydrite colloids is not available to the green alga R. subcapitata. Copyright © 2014 Elsevier Ltd. All rights reserved.

Osmotic consolidation of suspensions and gels

International Nuclear Information System (INIS)

Miller, K.T.; Zukoski, C.F.

1994-01-01

An osmotic method for the consolidation of suspensions of ceramic particles is demonstrated. Concentrated solutions of poly(ethylene oxide) are separated from a suspension of ceramic particles by a semipermeable membrane, creating a gradient in solvent chemical potential. Solvent passes from the suspension into the polymer solution, lowering its free energy and consolidating the suspension. Dispersions of stable 8-nm hydrous zirconia particles were consolidated to over 47% by volume. Suspensions of α-alumina in three states of aggregation (dispersed, weakly flocculated, and strongly flocculated) were consolidated to densities greater than or equal to those produced in conventional pressure filtration. Moreover, the as-consolidated alumina bodies were partially drained of fluid during the osmotic consolidation process, producing cohesive partially dried bodies with improved handling characteristics

Silver distribution and release from an antimicrobial denture base resin containing silver colloidal nanoparticles.

Science.gov (United States)

Monteiro, Douglas Roberto; Gorup, Luiz Fernando; Takamiya, Aline Satie; de Camargo, Emerson Rodrigues; Filho, Adhemar Colla Ruvolo; Barbosa, Debora Barros

2012-01-01

The aim of this study was to evaluate a denture base resin containing silver colloidal nanoparticles through morphological analysis to check the distribution and dispersion of these particles in the polymer and by testing the silver release in deionized water at different time periods. A Lucitone 550 denture resin was used, and silver nanoparticles were synthesized by reduction of silver nitrate with sodium citrate. The acrylic resin was prepared in accordance with the manufacturers' instructions, and silver nanoparticle suspension was added to the acrylic resin monomer in different concentrations (0.05, 0.5, and 5 vol% silver colloidal). Controls devoid of silver nanoparticles were included. The specimens were stored in deionized water at 37°C for 7, 15, 30, 60, and 120 days, and each solution was analyzed using atomic absorption spectroscopy. Silver was not detected in deionized water regardless of the silver nanoparticles added to the resin and of the storage period. Micrographs showed that with lower concentrations, the distribution of silver nanoparticles was reduced, whereas their dispersion was improved in the polymer. Moreover, after 120 days of storage, nanoparticles were mainly located on the surface of the nanocomposite specimens. Incorporation of silver nanoparticles in the acrylic resin was evidenced. Moreover, silver was not detected by the detection limit of the atomic absorption spectrophotometer used in this study, even after 120 days of storage in deionized water. Silver nanoparticles are incorporated in the PMMA denture resin to attain an effective antimicrobial material to help control common infections involving oral mucosal tissues in complete denture wearers. © 2011 by the American College of Prosthodontists.

Effect of colloidal aggregation on the sedimentation and rheological properties of tank waste

International Nuclear Information System (INIS)

Rector, D.R.; Bunker, B.C.

1995-09-01

Tank farm experience and work performed under the Tank Waste Treatment Science task of the Tank Waste Remediation System (TWRS) Pretreatment Technology Development Project indicate that colloidal interactions can have an enormous impact on tank waste processing. This report provides the theoretical and experimental background required to understand how such agglomeration phenomena control the sedimentation and theological behavior of colloidal tank wastes. First, the report describes the conditions under which the colloidal particles present in tank sludge are expected to aggregate. Computational models have been developed to predict solution conditions leading to agglomeration, and to predict the rate and size of aggregate growth. The models show that tank sludge should be heavily agglomerated under most baseline processing conditions. Second, the report describes models used to predict sedimentation rates and equilibrium sediment density profiles based on knowledge of agglomerate structures. The sedimentation models provide a self-consistent picture that explains the apparent discrepancies between bench-top experiments and tank-farm experience. Finally, both discrete and empirical models are presented that can be used to rationalize and predict the rheological properties of colloidal sludge suspensions. In all cases, model predictions are compared and contrasted with experimental results. The net results indicate that most of the observed behaviors of real sludges can be predicted, understood, and perhaps ultimately controlled by understanding a few key central concepts regarding agglomeration phenomena

Photoelastic colloidal gel for a high-sensitivity strain sensor

Science.gov (United States)

Pan, Hui; Chen, Zhixin; Zhu, Shenmin; Jiang, Chun; Zhang, Di

2018-04-01

Nanoparticles, having the ability to self-assemble into an ordered structure in their suspensions, analogous to liquid crystals, have attracted extensive attention. Herein, we report a new type of colloidal gel with an ordered crystal structure assembled from 1D and 2D nanoparticles. The material has high elasticity and, more interestingly, it shows significant photoelasticity. Its refractive index can be tuned under external stress and exhibits an ultra-wide dynamic range (Δn) of the order of 10-2. Due to the large Δn, the material shows an extremely high strain sensibility of 720 nm/ɛ, an order of magnitude higher than the reported ones.

From colloidal spheres to nanofibrils: extensional flow properties of mineral pigment and mixtures with micro and nanofibrils under progressive double layer suppression.

Science.gov (United States)

Dimic-Misic, Katarina; Hummel, Michael; Paltakari, Jouni; Sixta, Herbert; Maloney, Thad; Gane, Patrick

2015-05-15

Suspensions of mineral pigment and cellulose fibrillar derivatives are materials regularly found in the forest products industries, particularly in paper and board production. Many manufacturing processes, including forming and coating employ flow geometries incorporating extensional flow. Traditionally, colloidal mineral pigment suspensions have been considered to show little to no non-linear behaviour in extensional viscosity. Additionally, recently, nanofibrillar materials, such as microfibrillar (MFC) and nanofibrillar cellulose (NFC), collectively termed MNFC, have been confirmed by their failure to follow the Cox-Merz rule to behave more as particulate material rather than showing polymeric rheological properties when dispersed in water. Such suspensions and their mixtures are currently intensively investigated to enable them to generate likely enhanced composite material properties. The processes frequently involve exposure to increasing levels of ionic strength, coming either from the weak solubility of pigments, such as calcium carbonate, or retained salts arising from the feed fibre source processing. By taking the simple case of polyacrylate stabilised calcium carbonate suspension and comparing the extensional viscosity as a function of post extension capillary-induced Hencky strain on a CaBER extensional rheometer over a range of increasing salt concentration, it has been shown that the regime of constriction changes as the classic DLVO double layer is progressively suppressed. This change is seen to lead to a characteristic double (bimodal) measured viscosity response for flocculated systems. With this novel characteristic established, more complex mixed suspensions of calcium carbonate, clay and MNFC have been studied, and the effects of fibrils versus flocculation identified and where possible separated. This technique is suggested to enable a better understanding of the origin of viscoelasticity in these important emerging water-based suspensions

Anisotropic Model Colloids

NARCIS (Netherlands)

van Kats, C.M.

2008-01-01

The driving forces for fundamental research in colloid science are the ability to manage the material properties of colloids and to unravel the forces that play a role between colloids to be able to control and understand the processes where colloids play an important role. Therefore we are

Spontaneous formation of stringlike clusters and smectic sheets for colloidal rods confined in thin wedgelike gaps.

Science.gov (United States)

Maeda, Hideatsu; Maeda, Yoshiko

2013-08-20

Monodispersed colloidal rods of β-FeOOH with sizes ranging from 270 to 580 nm in length and 50 to 80 nm in width were synthesized. Narrow wedgelike gaps (0 to 700 nm in height) were formed around the inner bottom edge of the suspension glass cells. Optical microscopic observations revealed the formation of stringlike clusters of the rods and smectic sheets (by spontaneous side-by-side clustering of the strings) in the isotropic phase of the rod suspensions confined in narrow gaps; the electrolyte (HCl) concentrations of the suspensions are 5-40 mM, at which inter-rod interactions are attractive. The strings exhibit different colors that were used to investigate the structures of the strings with the help of interference color theory for thin films. The results are as follows. (1) The rods, lying flat on the gap bottom, are connected side-by-side and stacked upward to form stringlike clusters with different thicknesses depending on the gap height. (2) The stacking numbers (N(sr)) of the rods are estimated to be 1-5. With N(sr) increasing from 2 to 5, the volume fractions (ϕ) of the rods in the strings increased typically from 0.25-0.3 to 0.35-0.42 to reach limiting values (close to the ϕ values of the rods in the bulk smectic phase). (3) Unexpected low-ϕ strings are found in regions with an intermediate height in the gaps. These behaviors of ϕ may be caused by thermal fluctuations of the strings.

Colloid Detection in Natural Ground Water from Ruprechtov by Laser-Induced Breakdown Detection

Energy Technology Data Exchange (ETDEWEB)

Hauser, W.; Geckeis, H.; Goetz, R. [FZK - Inst. fuer Nukleare Entsorgung, Ka rlsruhe (Germany)]. e-mail: hauser@ine.fzk.de; Noseck, U. [Gesellschaft fuer Anlagen- und Reaktorsicherheit, D-38122 Braunschweig (Germany); Laciok, A. [Nuclear Research Inst. Rez plc, Waste and Environmental Management Dept., Husinec-Rez, PSC 250 68 (Czech Republic)

2007-06-15

A borehole ground water sampling system and a mobile laser-induced breakdown detection (LIBD) equipment for colloid detection combined with a geomonitoring unit have been applied to characterize the natural background colloid concentration in ground waters of the Ruprechtov natural analogue site (Czech Republic). Ground water has been sampled using steel cylinders. To minimize artifacts during ground water sampling the contact to atmospheric oxygen has been excluded. The ground water samples collected in this way are transported to the laboratory where they have been connected to a series of flow-through detection cells. Argon gas is used to press the ground water through these detection cells for colloid analysis (LIBD), pH, Eh, electrical conductivity and oxygen content. After the above mentioned analysis additional samples are taken for chemical analysis by ICP-AES, ICP-MS, IC- and DOC-detection. Our data obtained by in-situ- and laboratory- measurements point out that the natural colloid concentration found at the Ruprechtov site is a strong function of the ground water ionic strength. The LIBD determined natural background colloid concentrations found at Ruprechtov are compared with data of studies performed in Aespoe (Sweden) and Grimsel (Switzerland)

Natural colloidal P and its contribution to plant P uptake.

Science.gov (United States)

Montalvo, Daniela; Degryse, Fien; McLaughlin, Mike J

2015-03-17

Phosphorus (P) bioavailability depends on its concentration and speciation in solution. Andisols and Oxisols have very low soil solution concentration of free orthophosphate, as they contain high concentrations of strongly P-sorbing minerals (Al/Fe oxyhydroxides, allophanes). Free orthophosphate is the form of P taken up by plants, but it is not the only P species present in the soil solution. Natural colloidal P (P associated with Al, Fe, and organic matter of sizes ranging from 1 to 1000 nm) constitutes an important fraction of soil solution P in these soils; however, its availability has not been considered. We measured the uptake of P by wheat (Triticum aestivum) from radiolabeled nonfiltered (colloid-containing) and 3-kDa filtered (nearly colloid-free) soil-water extracts from Andisols and Oxisols. In the Andisol extracts, P uptake was up to 5-fold higher from the nonfiltered solutions than the corresponding 3-kDa filtered solutions. In the Oxisol extract, no difference in P uptake between both solutions was observed. Also the diffusional flux of P as measured with the DGT technique was larger in the nonfiltered than in the 3-kDa filtered solutions. Our results suggest that colloidal P from Andisols is not chemically inert and contributes to plant uptake of P.

Leaching of natural colloids from forest topsoils and their relevance for phosphorus mobility.

Science.gov (United States)

Missong, Anna; Holzmann, Stefan; Bol, Roland; Nischwitz, Volker; Puhlmann, Heike; V Wilpert, Klaus; Siemens, Jan; Klumpp, Erwin

2018-09-01

The leaching of P from the upper 20cm of forest topsoils influences nutrient (re-)cycling and the redistribution of available phosphate and organic P forms. However, the effective leaching of colloids and associated P forms from forest topsoils was so far sparsely investigated. We demonstrated through irrigation experiments with undisturbed mesocosm soil columns, that significant proportions of P leached from acidic forest topsoils were associated with natural colloids. These colloids had a maximum size of 400nm. By means of Field-flow fractionation the leached soil colloids could be separated into three size fractions. The size and composition was comparable to colloids present in acidic forest streams known from literature. The composition of leached colloids of the three size classes was dominated by organic carbon. Furthermore, these colloids contained large concentrations of P which amounted between 12 and 91% of the totally leached P depending on the type of the forest soil. The fraction of other elements leached with colloids ranged between 1% and 25% (Fe: 1-25%; C org : 3-17%; Al: leaching. Leaching of total and colloid-associated P from the forest surface soil did not increase with increasing bulk soil P concentrations and were also not related to tree species. The present study highlighted that colloid-facilitated P leaching can be of higher relevance for the P leaching from forest surface soils than dissolved P and should not be neglected in soil water flux studies. Copyright © 2018 Elsevier B.V. All rights reserved.

Hydrophilic/hydrophobic surface modification impact on colloid lithography: Schottky-like defects, dislocation, and ideal distribution

Science.gov (United States)

Burtsev, Vasilii; Marchuk, Valentina; Kugaevskiy, Artem; Guselnikova, Olga; Elashnikov, Roman; Miliutina, Elena; Postnikov, Pavel; Svorcik, Vaclav; Lyutakov, Oleksiy

2018-03-01

Nano-spheres lithography is actually considered as a powerful tool to manufacture various periodic structures with a wide potential in the field of nano- and micro-fabrication. However, during self-assembling of colloid microspheres, various defects and mismatches can appear. In this work the size and quality of single-domains of closed-packed polystyrene (PS), grown up on thin Au layers modified by hydrophilic or hydrophobic functional groups via diazonium chemistry was studied. The effects of the surface modification on the quality and single-domain size of polystyrene (PS) microspheres array were investigated and discussed. Modified surfaces were characterized using the AFM and wettability tests. PS colloidal suspension was deposited using the drop evaporation method. Resulted PS microspheres array was characterized using the SEM, AFM and confocal microscopy technique.

Hardening of particle/oil/water suspensions due to capillary bridges: Experimental yield stress and theoretical interpretation.

Science.gov (United States)

Danov, Krassimir D; Georgiev, Mihail T; Kralchevsky, Peter A; Radulova, Gergana M; Gurkov, Theodor D; Stoyanov, Simeon D; Pelan, Eddie G

2018-01-01

Suspensions of colloid particles possess the remarkable property to solidify upon the addition of minimal amount of a second liquid that preferentially wets the particles. The hardening is due to the formation of capillary bridges (pendular rings), which connect the particles. Here, we review works on the mechanical properties of such suspensions and related works on the capillary-bridge force, and present new rheological data for the weakly studied concentration range 30-55 vol% particles. The mechanical strength of the solidified capillary suspensions, characterized by the yield stress Y, is measured at the elastic limit for various volume fractions of the particles and the preferentially wetting liquid. A quantitative theoretical model is developed, which relates Y with the maximum of the capillary-bridge force, projected on the shear plane. A semi-empirical expression for the mean number of capillary bridges per particle is proposed. The model agrees very well with the experimental data and gives a quantitative description of the yield stress, which increases with the rise of interfacial tension and with the volume fractions of particles and capillary bridges, but decreases with the rise of particle radius and contact angle. The quantitative description of capillary force is based on the exact theory and numerical calculation of the capillary bridge profile at various bridge volumes and contact angles. An analytical formula for Y is also derived. The comparison of the theoretical and experimental strain at the elastic limit reveals that the fluidization of the capillary suspension takes place only in a deformation zone of thickness up to several hundred particle diameters, which is adjacent to the rheometer's mobile plate. The reported experimental results refer to water-continuous suspension with hydrophobic particles and oily capillary bridges. The comparison of data for bridges from soybean oil and hexadecane surprisingly indicate that the yield strength is

PCR detection of groundwater bacteria associated with colloidal transport

Energy Technology Data Exchange (ETDEWEB)

Cruz-Perez, P.; Stetzenbach, L.D.; Alvarez, A.J.

1996-02-29

Colloidal transport may increase the amount of contaminant material than that which could be transported by water flow alone. The role of colloids in groundwater contaminant transport is complicated and may involve many different processes, including sorption of elements onto colloidal particles, coagulation/dissolution, adsorption onto solid surfaces, filtration, and migration. Bacteria are known to concentrate minerals and influence the transport of compounds in aqueous environments and may also serve as organic colloids, thereby influencing subsurface transport of radionuclides and other contaminants. The initial phase of the project consisted of assembling a list of bacteria capable of sequestering or facilitating mineral transport. The development and optimization of the PCR amplification assay for the detection of the organisms of interest, and the examination of regional groundwaters for those organisms, are presented for subsequent research.

PCR detection of groundwater bacteria associated with colloidal transport

International Nuclear Information System (INIS)

Cruz-Perez, P.; Stetzenbach, L.D.; Alvarez, A.J.

1996-01-01

Colloidal transport may increase the amount of contaminant material than that which could be transported by water flow alone. The role of colloids in groundwater contaminant transport is complicated and may involve many different processes, including sorption of elements onto colloidal particles, coagulation/dissolution, adsorption onto solid surfaces, filtration, and migration. Bacteria are known to concentrate minerals and influence the transport of compounds in aqueous environments and may also serve as organic colloids, thereby influencing subsurface transport of radionuclides and other contaminants. The initial phase of the project consisted of assembling a list of bacteria capable of sequestering or facilitating mineral transport. The development and optimization of the PCR amplification assay for the detection of the organisms of interest, and the examination of regional groundwaters for those organisms, are presented for subsequent research

Green synthesis of silver nanoparticles and silver colloidal solutions

International Nuclear Information System (INIS)

Nguyen Thi Phuong Phong; Ngo Hoang Minh; Ngo Vo Ke Thanh; Dang Mau Chien

2009-01-01

In this paper, silver colloidal solutions have been synthesized rapidly in green conditions by using microwave irradiation and non-toxic chemistry substances (acid oxalic, silver nitrate, polyvinyl pyrolidone (PVP; Mw = 55 000)). The particle size and morphology of these solutions can be controlled by altering several factors like the time, the power of microwave exposure, and the ratio of silver oxalate and PVP etc. The silver nanoparticles were fabricated by thermal decomposition of silver oxalate. The synthesized silver colloidal solutions and silver nanoparticles were characterized by several analytical techniques like UV- VIS, XRD, TEM, FESEM/EDS and ICP-AAS studies. Finally, we used the synthesized silver colloidal solutions for antibacterial purpose. The obtained results showed that the synthesized silver colloidal solutions, even at very low concentrations, have highly efficient anti-bacterial property.

Long-term colloidal stability of 10 carbon nanotube types in the absence/presence of humic acid and calcium

International Nuclear Information System (INIS)

Schwyzer, Irène; Kaegi, Ralf; Sigg, Laura; Smajda, Rita; Magrez, Arnaud; Nowack, Bernd

2012-01-01

The colloidal stabilities of ten carbon nanotubes (CNTs) having varying physico-chemical properties were compared in long-term experiments. The presence of Suwannee River Humic Acid (SRHA) increased the fraction of CNTs in the supernatants (4–88% for the various CNT types) after addition in pre-dispersed form and 20 days of shaking and 5 days of settling. These suspensions were monomodal, containing individually suspended CNTs with highly negative surface charges. Calcium (2 mM) removed most of the CNT types from the supernatant, due to CNT-agglomerate formation initiated by reduction in surface charge. The amount of SRHA adsorbed to the different CNT types did not correlate (r 2 < 0.1) with the percentage of CNTs remaining in suspension. Multiple linear regression analysis revealed that the oxygen content and the diameter of the CNTs significantly influenced the percentage of stabilized CNTs, resulting in an increased fraction of functionalized and large-diameter CNTs that remained in suspension. Highlights: ► Ten different CNT types with varying physico-chemical properties were used. ► The presence of SRHA increased the fraction of CNTs in the supernatants for all CNT-types. ► The O-content and diameter of the CNTs influenced the percentage of CNTs stabilized. ► Functionalization and large diameter made CNTs resistant against Ca flocculation. - The long-term colloidal stability of 10 different CNT types in the presence of humic acid was dependent on oxygen content and diameter of the CNTs.

Short- and long-range correlated motion observed in colloidal glasses and liquids

International Nuclear Information System (INIS)

Weeks, Eric R; Crocker, John C; Weitz, D A

2007-01-01

We use a confocal microscope to examine the motion of individual particles in a dense colloidal suspension. Close to the glass transition, particle motion is strongly spatially correlated. The correlations decay exponentially with particle separation, yielding a dynamic length scale of O(2-3σ) (in terms of particle diameter σ). This length scale grows modestly as the glass transition is approached. Further, the correlated motion exhibits a strong spatial dependence on the pair correlation function g(r). Motion within glassy samples is weakly correlated, but with a larger spatial scale for this correlation

Synthesis and characterization of Nb_2O_5 by a colloidal route

International Nuclear Information System (INIS)

Falk, G.S.; Borlaf, M.; Oliveira, A.P. Novaes de; Rodrigues Neto, J.B.; Hotza, D.; Moreno, R.

2014-01-01

The niobium pentoxide (Nb_2O_5) is known to be a polymorphic ceramic semiconductor and display features, which makes it a potential candidate in the field of photocatalysis. In this paper, we evaluate a colloidal route for the synthesis of Nb_2O_5. The properties of the suspension and the powder obtained were determined by analysis of particle size, zeta potential, thermogravimetric and differential thermal analysis (TG-DTA) and X-ray diffraction (XRD). The results indicated that the particle size was 0.3 μm and at pHs between 8 and 9, stable suspensions were obtained. Through the XRD results it was observed that the synthesized powder is amorphous and that at 300°C/1h niobic acid (HNbO_3) crystallizes, which after calcination at 450, 650, 850 and 1050 deg C/1h, turns into Nb_2O_5 with different crystalline structures. (author)

Laboratory investigation of the factors impact on bubble size, pore blocking and enhanced oil recovery with aqueous Colloidal Gas Aphron.

Science.gov (United States)

Shi, Shenglong; Wang, Yefei; Li, Zhongpeng; Chen, Qingguo; Zhao, Zenghao

Colloidal Gas Aphron as a mobility control in enhanced oil recovery is becoming attractive; it is also designed to block porous media with micro-bubbles. In this paper, the effects of surfactant concentration, polymer concentration, temperature and salinity on the bubble size of the Colloidal Gas Aphron were studied. Effects of injection rates, Colloidal Gas Aphron fluid composition, heterogeneity of reservoir on the resistance to the flow of Colloidal Gas Aphron fluid through porous media were investigated. Effects of Colloidal Gas Aphron fluid composition and temperature on residual oil recovery were also studied. The results showed that bubble growth rate decreased with increasing surfactant concentration, polymer concentration, and decreasing temperature, while it decreased and then increased slightly with increasing salinity. The obvious increase of injection pressure was observed as more Colloidal Gas Aphron fluid was injected, indicating that Colloidal Gas Aphron could block the pore media effectively. The effectiveness of the best blend obtained through homogeneous sandpack flood tests was modestly improved in the heterogeneous sandpack. The tertiary oil recovery increased 26.8 % by Colloidal Gas Aphron fluid as compared to 20.3 % by XG solution when chemical solution of 1 PV was injected into the sandpack. The maximum injected pressure of Colloidal Gas Aphron fluid was about three times that of the XG solution. As the temperature increased, the Colloidal Gas Aphron fluid became less stable; the maximum injection pressure and tertiary oil recovery of Colloidal Gas Aphron fluid decreased.

Progress report on colloid-facilitated transport at Yucca Mountain: Yucca Mountain site characterization program milestone 3383

International Nuclear Information System (INIS)

Triay, I.R.; Degueldre, C.; Wistrom, A.O.; Cotter, C.R.; Lemons, W.W.

1996-06-01

To assess colloid-facilitated radionuclide transport in groundwaters at the potential nuclear waste repository at Yucca Mountain, it is very important to understand the generation and stability of colloids, including naturally occurring colloids. To this end, we measured the colloid concentration in waters from Well J-13, which is on the order of 106 particles per milliliter (for particle sizes larger than 100 manometers). At this low particle loading, the sorption of radionuclides to colloids would have to be extremely high before the colloids could carry a significant amount of radionuclides from the repository to the accessible environment. We also performed aggregation experiments to evaluate the stability of silica (particle diameter: 85 nm) and clay colloids (particle diameter: 140 nm) as a function of ionic strength in a carbonate-rich synthetic groundwater. When the concentration of electrolyte is increased to induce aggregation, the aggregation is irreversible and the rate of aggregation increases with increasing electrolyte strength. We used autocorrelation photon spectroscopy to estimate the rate of particle aggregation for both types of colloids. By relating the measured aggregation rate to the Smoluchowski rate expression, we determined the stability ratio, W. Aggregation of silica particles and kaolinite clay particles decreased dramatically for an electrolyte concentration, C NaCl , below 300 mM and 200 mM, respectively

Colloid-facilitated radionuclide transport in the fractured rock: effects of decay chain and limited matrix diffusion

International Nuclear Information System (INIS)

Park, J. B.; Park, J. W.; Lee, E. Y.; Kim, C. R.

2002-01-01

Colloid-facilitated radionuclide transport in the fractured rock is studies by considering radioactive decay chain and limited matrix diffusion into surrounding porous media. Semi-analytical solution in the Laplace domain is obtained from the mass balance equation of radionuclides and colloid particles. Numerical inversion of the Laplace solution is used to get the concentration profiles both in a fracture and in rock matrix. There issues are analyzed for the radionuclide concentration in a fracture by 1) formation constant of pseudo-colloid, 2) filtration coefficient of radio-colloid and 3) effective diffusion depth into the surrounding porous rock media

Flocculation of colloidal clay by bacterial polysaccharides: effect of macromolecule charge and structure.

Science.gov (United States)

Labille, J; Thomas, F; Milas, M; Vanhaverbeke, C

2005-04-01

The molecular mechanism of montmorillonite flocculation by bacterial polysaccharides was investigated, with special emphasis on the effect of carboxylic charges in the macromolecules on the mechanisms of interaction with the clay surface. An indirect way to quantify the energy of interaction was used, by comparing the flocculation ability of variously acidic polysaccharides. Data on tensile strength of aggregates in diluted suspension were collected by timed size measurements in the domain 0.1-600 microm, using laser diffraction. The flow behavior of settled aggregates was studied by rheology measurements. Flocculation of colloidal clay suspension by polysaccharides requires cancelling of the electrostatic repulsions by salts, which allows approach of clay surfaces close enough to be bridged by adsorbing macromolecules. The amount of acidic charges of the polysaccharides, and especially their location in the molecular structure, governs the bridging mechanism and the resulting tensile strength of the aggregates. The exposure of carboxylate groups located on side chains strongly promotes flocculation. In turn, charges located on the backbone of the polysaccharide are less accessible to interaction, and the flocculation ability of such polysaccharides is lowered. Measurements at different pH indicate that adsorption of acidic polysaccharides occurs via electrostatic interactions on the amphoteric edge surface of clay platelets, whereas neutral polysaccharides rather adsorb via weak interactions. Increased tensile strength in diluted aggregates due to strong surface interactions results in proportionally increased viscosity of the concentrated aggregates.

Sorption behavior of cesium onto bentonite colloid

International Nuclear Information System (INIS)

Iijima, Kazuki; Masuda, Tsuguya; Tomura, Tsutomu

2004-01-01

It is considered that bentonite colloid might be generated from bentonite which will be used as buffer material in geological disposal system, and can facilitate the migration of radionuclides by means of sorption. In order to examine this characteristic, sorption and desorption experiments of Cs onto bentonite colloid were carried out to obtain its distribution coefficient (Kd) and information on the reversibility of its sorption. In addition, particle size distribution and shape of colloid were investigated and their effect on the sorption behavior was discussed. Kds for Cs were around 20 m 3 /kg for sorption and 30 m 3 /kg for desorption, in which sorbed Cs was desorbed by 8.4x10 -4 mol/l of NaCl solution. These values did not show any dependencies on Cs concentration and duration of sorption and desorption. The first 20% of sorbed Cs was desorbed reversibly at least. Most of colloidal particles were larger than 200 nm and TEM micrographs showed they had only several sheets of the clay crystal. Obtained Kds for colloidal bentonite were larger than those for powdered bentonite. This can be caused by difference of competing ions in the solution, characteristics of contained smectite, or sorption site density. (author)

On the influence of the hydrodynamic interactions on the aggregation rate of magnetic spheres in a dilute suspension

International Nuclear Information System (INIS)

Cunha, F.R.; Couto, H.L.G.

2011-01-01

Magnetostatic attraction may lead to formation of aggregates in stable colloidal magnetic suspensions and magneto-rheological suspensions. The aggregation problem of magnetic composites under differential sedimentation is a key problem in the control of the instability of non-Brownian suspensions. Against these attractive forces are the electrostatic repulsion and the hydrodynamic interactions acting as stabilizing effects to the suspension. This work concerns an investigation of the pairwise interaction of magnetic particles in a dilute sedimenting suspension. We focus attention on suspensions where the Peclet number is large (negligible Brownian motion) and where the Reynolds number (negligible inertia) is small. The suspension is composed of magnetic micro-spheres of different radius and density immersed in a Newtonian fluid moving under the action of gravity. The theoretical calculations are based on direct computations of the hydrodynamic and the magnetic interactions among the rigid spheres in the regime of low particle Reynolds number. From the limiting trajectory in which aggregation occurs, we calculate the collision efficiency, representing the dimensionless rate at which aggregates are formed. The numerical results show clear evidence that the hydrodynamic interactions are of fundamental relevance in the process of magnetic particle aggregation. We compare the stabilizing effects between electrostatic repulsion and hydrodynamic interactions.

On the influence of the hydrodynamic interactions on the aggregation rate of magnetic spheres in a dilute suspension

Energy Technology Data Exchange (ETDEWEB)

Cunha, F.R., E-mail: frcunha@unb.b [Universidade de Brasilia, Faculdade de Tecnologia, Depto. de Engenharia Mecanica, Grupo de Mecanica dos Fluidos de Escoamentos Complexos - VORTEX, Campus Universitario Darcy Ribeiro, 70910-900, Brasilia, DF (Brazil); Couto, H.L.G. [Universidade de Brasilia, Faculdade de Tecnologia, Depto. de Engenharia Mecanica, Grupo de Mecanica dos Fluidos de Escoamentos Complexos - VORTEX, Campus Universitario Darcy Ribeiro, 70910-900, Brasilia, DF (Brazil)

2011-01-15

Magnetostatic attraction may lead to formation of aggregates in stable colloidal magnetic suspensions and magneto-rheological suspensions. The aggregation problem of magnetic composites under differential sedimentation is a key problem in the control of the instability of non-Brownian suspensions. Against these attractive forces are the electrostatic repulsion and the hydrodynamic interactions acting as stabilizing effects to the suspension. This work concerns an investigation of the pairwise interaction of magnetic particles in a dilute sedimenting suspension. We focus attention on suspensions where the Peclet number is large (negligible Brownian motion) and where the Reynolds number (negligible inertia) is small. The suspension is composed of magnetic micro-spheres of different radius and density immersed in a Newtonian fluid moving under the action of gravity. The theoretical calculations are based on direct computations of the hydrodynamic and the magnetic interactions among the rigid spheres in the regime of low particle Reynolds number. From the limiting trajectory in which aggregation occurs, we calculate the collision efficiency, representing the dimensionless rate at which aggregates are formed. The numerical results show clear evidence that the hydrodynamic interactions are of fundamental relevance in the process of magnetic particle aggregation. We compare the stabilizing effects between electrostatic repulsion and hydrodynamic interactions.

Characterization and Correlation of Particle-Level Interactions to the Macroscopic Rheology of Powders, Granular Slurries, and Colloidal Suspensions

Energy Technology Data Exchange (ETDEWEB)

Poloski, Adam P.; Daniel, Richard C.; Rector, David R.; Bredt, Paul R.; Buck, Edgar C.; Berg, John C.; Saez, Avelino E.

2006-09-29

Hanford TRU tank sludges are complex mixtures of undissolved minerals and salt solids in an aqueous phase of high ionic strength. They show complex rheological behavior resulting from interactions at the macroscopic level, such as interparticle friction between grains in the coarse fraction, as well as from interactions at the nano-scale level, such as the agglomeration of colloidal particles. An understanding of how phenomena such as interparticle friction and aggregate stability under shear will allow better control of Hanford TRU tank sludges being processed for disposal. The project described in this report had two objectives. The first was to understand the physical properties and behavior of the Hanford transuranic (TRU) tank sludges under conditions that might exist during retrieval, treatment, packaging, and transportation for disposal at the Waste Isolation Pilot Plant (WIPP). The second objective was to develop a fundamental understanding of sludge physical properties by correlating the macroscopic behavior with interactions occurring at the particle/colloidal scale. These objectives were accomplished by: 1) developing continuum models for coarse granular slurries and 2) studying the behavior of colloidal agglomerates under shear and under irradiation.

Dissolved and colloidal trace elements in the Mississippi River Delta outflow after Hurricanes Katrina and Rita

Science.gov (United States)

Shim, Moo-Joon; Swarzenski, Peter W.; Shiller, Alan M.

2012-01-01

The Mississippi River delta outflow region is periodically disturbed by tropical weather systems including major hurricanes, which can terminate seasonal bottom water hypoxia and cause the resuspension of shelf bottom sediments which could result in the injection of trace elements into the water column. In the summer of 2005, Hurricanes Katrina and Rita passed over the Louisiana Shelf within a month of each other. Three weeks after Rita, we collected water samples in the Mississippi River delta outflow, examining the distributions of trace elements to study the effect of Hurricanes Katrina and Rita. We observed limited stratification on the shelf and bottom waters that were no longer hypoxic. This resulted, for instance, in bottom water dissolved Mn being lower than is typically observed during hypoxia, but with concentrations still compatible with Mn–O2 trends previously reported. Interestingly, for no element were we able to identify an obvious effect of sediment resuspension on its distribution. In general, elemental distributions were compatible with previous observations in the Mississippi outflow system. Co and Re, which have not been reported for this system previously, showed behavior consistent with other systems: input for Co likely from desorption and conservative mixing for Re. For Cs, an element for which there is little information regarding its estuarine behavior, conservative mixing was also observed. Our filtration method, which allowed us to distinguish the dissolved (<0.02 μm) from colloidal (0.02–0.45 μm) phase, revealed significant colloidal fractions for Fe and Zn, only. For Fe, the colloidal phase was the dominant fraction and was rapidly removed at low salinity. Dissolved Fe, in contrast, persisted out to mid-salinities, being removed in a similar fashion to nitrate. This ability to distinguish the smaller Fe (likely dominantly organically complexed) from larger colloidal suspensates may be useful in better interpreting the

Dynamic localization and shear-induced hopping of particles: A way to understand the rheology of dense colloidal dispersions

International Nuclear Information System (INIS)

Jiang, Tianying; Zukoski, Charles F.

2014-01-01

For decades, attempts have been made to understand the formation of colloidal glasses and gels by linking suspension mechanics to particle properties where details of size, shape, and spatial dependencies of pair potentials present a bewildering array of variables that can be manipulated to achieve observed properties. Despite the range of variables that control suspension properties, one consistent observation is the remarkably similarity of flow properties observed as particle properties are varied. Understanding the underlying origins of the commonality in those behaviors (e.g., shear-thinning with increasing stress, diverging zero shear rate viscosity with increasing volume fraction, development of a dynamic yield stress plateau with increases in volume faction or strength of attraction, development of two characteristic relaxation times probed in linear viscoelasticity, the creation of a rubbery plateau modulus at high strain frequencies, and shear-thickening) remains a challenge. Recently, naïve mode coupling and dynamic localization theories have been developed to capture collective behavior giving rise to formation of colloidal glasses and gels. This approach characterizes suspension mechanics of strongly interacting particles in terms of sluggish long-range particle diffusion modulated by varying particle interactions and volume fraction. These theories capture the scaling of the modulus with the volume fraction and strength of interparticle attraction, the frequency dependence of the moduli at the onset of the gel/glass transition, together with the divergence of the zero shear rate viscosity and cessation of diffusivity for hard sphere systems as close packing is approached. In this study, we explore the generality of the predictions of dynamic localization theory for systems of particles composed of bimodal particle size distributions experiencing weak interactions. We find that the mechanical properties of these suspensions are well captured within

Dynamic localization and shear-induced hopping of particles: A way to understand the rheology of dense colloidal dispersions

Energy Technology Data Exchange (ETDEWEB)

Jiang, Tianying; Zukoski, Charles F., E-mail: czukoski@illinois.edu [Department of Chemical and Biomolecular Engineering, University of Illinois Urbana-Champaign, Urbana, Illinois 61801 (United States)

2014-09-01

For decades, attempts have been made to understand the formation of colloidal glasses and gels by linking suspension mechanics to particle properties where details of size, shape, and spatial dependencies of pair potentials present a bewildering array of variables that can be manipulated to achieve observed properties. Despite the range of variables that control suspension properties, one consistent observation is the remarkably similarity of flow properties observed as particle properties are varied. Understanding the underlying origins of the commonality in those behaviors (e.g., shear-thinning with increasing stress, diverging zero shear rate viscosity with increasing volume fraction, development of a dynamic yield stress plateau with increases in volume faction or strength of attraction, development of two characteristic relaxation times probed in linear viscoelasticity, the creation of a rubbery plateau modulus at high strain frequencies, and shear-thickening) remains a challenge. Recently, naïve mode coupling and dynamic localization theories have been developed to capture collective behavior giving rise to formation of colloidal glasses and gels. This approach characterizes suspension mechanics of strongly interacting particles in terms of sluggish long-range particle diffusion modulated by varying particle interactions and volume fraction. These theories capture the scaling of the modulus with the volume fraction and strength of interparticle attraction, the frequency dependence of the moduli at the onset of the gel/glass transition, together with the divergence of the zero shear rate viscosity and cessation of diffusivity for hard sphere systems as close packing is approached. In this study, we explore the generality of the predictions of dynamic localization theory for systems of particles composed of bimodal particle size distributions experiencing weak interactions. We find that the mechanical properties of these suspensions are well captured within

Characterization of natural colloids sampled from a fractured granite groundwater

Energy Technology Data Exchange (ETDEWEB)

Baik, Min Hoon; Keum, Dong Kwon; Hahn, Pil Soo [Korea Atomic Energy Research Institute, Taejeon (Korea); Vilks, Peter [AECL Whiteshell Laboratories (Canada)

2000-02-01

This study was carried out as a part of international joint study of KAERI with AECL. The main purpose of this study is to analyze the physicochemical characteristics and sorption properties of natural colloids sampled from the deep fractured granite groundwater located in the Underground Research Laboratory (URL) of AECL. Physicochemical characteristics such as composition, size distribution, and concentrations of natural colloids was analyzed. This study will be basic data for the analysis of the effect of colloids on the radionuclide migration in a geological medium. This study may provide information for the evaluation of the roles and effects of colloids in the safety and performance assessment of a possible future radioactive waste repository. 20 refs., 8 figs., 8 tabs. (Author)

Self-assembly of patchy colloidal dumbbells

NARCIS (Netherlands)

Avvisati, Guido|info:eu-repo/dai/nl/407630198; Vissers, Teun|info:eu-repo/dai/nl/304829943; Dijkstra, Marjolein|info:eu-repo/dai/nl/123538807

2015-01-01

We employ Monte Carlo simulations to investigate the self-assembly of patchy colloidal dumbbells interacting via a modified Kern-Frenkel potential by probing the system concentration and dumbbell shape. We consider dumbbells consisting of one attractive sphere with diameter sigma(1) and one

Erbium-implanted silica colloids with 80% luminescence quantum efficiency

Science.gov (United States)

Slooff, L. H.; de Dood, M. J. A.; van Blaaderen, A.; Polman, A.

2000-06-01

Silica colloids with a diameter of 240-360 nm, grown by wet chemical synthesis using ethanol, ammonia, water, and tetraethoxysilane, were implanted with 350 keV Er ions, to peak concentrations of 0.2-1.1 at. % and put onto a silicon or glass substrate. After annealing at 700-900 °C the colloids show clear room-temperature photoluminescence at 1.53 μm, with lifetimes as high as 17 ms. By comparing data of different Er concentrations, the purely radiative lifetime is estimated to be 20-22 ms, indicating a high quantum efficiency of about 80%. This high quantum efficiency indicates that, after annealing, the silica colloids are almost free of OH impurities. Spinning a layer of polymethylmethacrylate over the silica spheres results in an optically transparent nanocomposite layer, that can be used as a planar optical waveguide amplifier at 1.5 μm that is fully compatible with polymer technology.

Cream formulation impact on topical administration of engineered colloidal nanoparticles.

Directory of Open Access Journals (Sweden)

Benedetta Santini

Full Text Available In order to minimize the impact of systemic toxicity of drugs in the treatment of local acute and chronic inflammatory reactions, the achievement of reliable and efficient delivery of therapeutics in/through the skin is highly recommended. While the use of nanoparticles is now an established practice for drug intravenous targeted delivery, their transdermal penetration is still poorly understood and this important administration route remains almost unexplored. In the present study, we have synthesized magnetic (iron oxide nanoparticles (MNP coated with an amphiphilic polymer, developed a water-in-oil emulsion formulation for their topical administration and compared the skin penetration routes with the same nanoparticles deposited as a colloidal suspension. Transmission and scanning electron microscopies provided ultrastructural evidence that the amphiphilic nanoparticles (PMNP cream formulation allowed the efficient penetration through all the skin layers with a controllable kinetics compared to suspension formulation. In addition to the preferential follicular pathway, also the intracellular and intercellular routes were involved. PMNP that crossed all skin layers were quantified by inductively coupled plasma mass spectrometry. The obtained data suggests that combining PMNP amphiphilic character with cream formulation improves the intradermal penetration of nanoparticles. While PMNP administration in living mice via aqueous suspension resulted in preferential nanoparticle capture by phagocytes and migration to draining lymph nodes, cream formulation favored uptake by all the analyzed dermis cell types, including hematopoietic and non-hematopoietic. Unlike aqueous suspension, cream formulation also favored the maintenance of nanoparticles in the dermal architecture avoiding their dispersion and migration to draining lymph nodes via afferent lymphatics.

Geometrical analysis of suspension flows near jamming

Science.gov (United States)

Wyart, Matthieu

2012-02-01

The viscosity of suspensions was computed early on by Einstein and Batchelor in the dilute regime. At high density however, their rheology remains mystifying. As the packing fraction increases, steric hindrance becomes dominant and particles move under stress in a more and more coordinated way. Eventually, the viscosity diverges as the suspension jams into an amorphous solid. Such a jamming transition is reminiscent of critical points: the rheology displays scaling and a diverging length scale. Jamming bear similarities with the glass transition where steric hindrance is enhanced under cooling, and where the dynamics is also observed to become more and more collective as it slows down. In all these examples, understanding the nature of the collective dynamics and the associated rheology remains a challenge. Recent progress has been made however on a related problem, the unjamming transition where a solid made of repulsive soft particles is isotropically decompressed toward vanishing pressure. In this situation various properties of the amorphous solid, such as elasticity, transport or force propagation, display scaling with the distance to threshold. Theoretically these observations can be shown to stem from the presence of soft modes in the vibrational spectrum, a result that can be extended to thermal colloidal glasses as well. Here we focus on particles driven by shear at zero temperature. We show that if hydrodynamical interactions are neglected an analogy can be made between the rheology of such a suspension and the elasticity of simple networks, building a link between the jamming and the unjamming transition. This analogy enables us to unify in a common framework key aspects of the elasticity of amorphous solids with the rheology of dense suspensions, and to relate features of the latter to the geometry of configurations visited under flow.

Novel forms of colloidal self-organization in temporally and spatially varying external fields: from low-density network-forming fluids to spincoated crystals

Science.gov (United States)

Yethiraj, Anand

2010-03-01

External fields affect self-organization in Brownian colloidal suspensions in many different ways [1]. High-frequency time varying a.c. electric fields can induce effectively quasi-static dipolar inter-particle interactions. While dipolar interactions can provide access to multiple open equilibrium crystal structures [2] whose origin is now reasonably well understood, they can also give rise to competing interactions on short and long length scales that produce unexpected low-density ordered phases [3]. Farther from equilibrium, competing external fields are active in colloid spincoating. Drying colloidal suspensions on a spinning substrate produces a ``perfect polycrystal'' - tiny polycrystalline domains that exhibit long-range inter-domain orientational order [4] with resultant spectacular optical effects that are decoupled from single-crystallinity. High-speed movies of drying crystals yield insights into mechanisms of structure formation. Phenomena arising from multiple spatially- and temporally-varying external fields can give rise to further control of order and disorder, with potential application as patterned (photonic and magnetic) materials. [4pt] [1] A. Yethiraj, Soft Matter 3, 1099 (2007). [2] A. Yethiraj, A. van Blaaderen, Nature 421, 513 (2003). [3] A.K. Agarwal, A. Yethiraj, Phys. Rev. Lett ,102, 198301 (2009). [4] C. Arcos, K. Kumar, W. Gonz'alez-Viñas, R. Sirera, K. Poduska, A. Yethiraj, Phys. Rev. E ,77, 050402(R) (2008).

The role of quench rate in colloidal gels.

Science.gov (United States)

Royall, C Patrick; Malins, Alex

2012-01-01

Interactions between colloidal particles have hitherto usually been fixed by the suspension composition. Recent experimental developments now enable the control of interactions in situ. Here we use Brownian dynamics simulations to investigate the effect of controlling interactions upon gelation, by "quenching" the system from an equilibrium fluid to a gel. We find that, contrary to the normal case of an instantaneous quench, where the local structure of the gel is highly disordered, controlled quenching results in a gel with a much higher degree of local order. Under sufficiently slow quenching, local crystallisation is found, which is strongly enhanced when a monodisperse system is used. The higher the degree of local order, the smaller the mean squared displacement, indicating an enhancement of gel stability.

Simultaneous transport of synthetic colloids and a nonsorbing solute through single saturated natural fractures

International Nuclear Information System (INIS)

Reimus, P.W.; Robinson, B.A.; Nuttall, H.E.; Kale, R.

1994-01-01

Tracer transport experiments involving colloids that showed little tendency to attach to rock surfaces and a nonsorbing solute (iodide) -were conducted in three different well-characterized natural fractures in tuff. The colloids always arrived earlier in the effluent than the iodide, which we believe is evidence of (1) hydrodynamic chromatography and/or (2) the fact that the colloids experience a smaller effective volume in the fracture because they diffuse too slowly to enter low-velocity regions (dead zones) along the rough fracture walls. The iodide also approached the inlet concentration in the effluent more slowly than the colloids, with the concentration at a given elution volume being greater at higher flow rates. By contrast, the rate of approach of the colloid concentration to the inlet concentration did not vary with flow rate. We attribute this behavior to matrix diffusion of the iodide, with the colloids being too large/nondiffusive to experience this phenomenon. Dispersion of all tracers was greatest in the fracture of widest average aperture and least in the fracture of narrowest aperture, which is consistent with Taylor dispersion theory. The tracer experiments were modeled/interpreted using a three-step approach that involved (1) estimating the aperture distribution in each fracture using surface profiling techniques, (2) predicting the flow field in the fractures using a localized parallel-plate approximation, and (3) predicting tracer transport in the fractures using particle-tracking techniques. Although considered preliminary at this time, the model results were in qualitative agreement with the experiments

Preparation of silver colloid and enhancement of dispersion stability in organic solvent

International Nuclear Information System (INIS)

Kim, Ki Young; Choi, Young Tai; Seo, Dae Jong; Park, Seung Bin

2004-01-01

Silver colloid of nanometer size was prepared in liquid phase by a reduction method. AgNO 3 , FeSO 4 .7H 2 O, and Na 3 C 6 H 5 O 7 .2H 2 O were used as silver precursor, reducing agent and dispersing agent, respectively. As precursor concentration was decreased or the concentration of dispersing agent was increased, the prepared particle size was decreased from 180 nm to 20 nm. Apparently, the particle size seemed to be decreased with the increase of stirring rate, but it was confirmed by TEM that the size of primary particle remained the same. This result indicates that the uniformity of precursor concentration in the reactor affects the particle size and the stirring rate should be kept higher than the critical value to prevent the agglomeration of particles. In order to make the dispersion stability of the prepared silver colloid maintained even in non-polar organic solvent, electrodialysis technique was applied. As ionic species in colloidal solution were removed by electrodialysis, the dispersability of the colloid in the organic solvent of long carbon chain was confirmed to be increased

Antibacterial Activity of Electrochemically Synthesized Colloidal Silver Nanoparticles Against Hospital-Acquired Infections

Science.gov (United States)

Thuc, Dao Tri; Huy, Tran Quang; Hoang, Luc Huy; Hoang, Tran Huy; Le, Anh-Tuan; Anh, Dang Duc

2017-06-01

This study evaluated the antibacterial activity of electrochemically synthesized colloidal silver nanoparticles (AgNPs) against hospital-acquired infections. Colloidal AgNPs were synthesized via a single process using bulk silver bars, bi-distilled water, trisodium citrate, and direct current voltage at room temperature. Colloidal AgNPs were characterized by transmission electron microscopy, field-emission scanning electron microscopy, and energy-dispersive x-ray analyses. The antibacterial activity of colloidal AgNPs against four bacterial strains isolated from clinical samples, including methicillin-resistant Staphylococcus aureus, Escherichia coli O157:H7, multidrug-resistant Pseudomonas aeruginosa, and carbapenem-resistant Klebsiella pneumonia, was evaluated by disc diffusion, minimum inhibitory concentration (MIC), and ultrathin sectioning electron microscopy. The results showed that the prepared AgNPs were 19.7 ± 4.3 nm in size, quasi-spherical, and of high purity. Zones of inhibition approximately 6-10 mm in diameter were found, corresponding to AgNPs concentrations of 50 μg/mL to 100 μg/mL. The MIC results revealed that the antibacterial activity of the prepared AgNPs was strongly dependent on the concentration and strain of the tested bacteria.

Rheological study of two-dimensional very anisometric colloidal particle suspensions: from shear-induced orientation to viscous dissipation.

Science.gov (United States)

Philippe, A M; Baravian, C; Bezuglyy, V; Angilella, J R; Meneau, F; Bihannic, I; Michot, L J

2013-04-30

In the present study, we investigate the evolution with shear of the viscosity of aqueous suspensions of size-selected natural swelling clay minerals for volume fractions extending from isotropic liquids to weak nematic gels. Such suspensions are strongly shear-thinning, a feature that is systematically observed for suspensions of nonspherical particles and that is linked to their orientational properties. We then combined our rheological measurements with small-angle X-ray scattering experiments that, after appropriate treatment, provide the orientational field of the particles. Whatever the clay nature, particle size, and volume fraction, this orientational field was shown to depend only on a nondimensional Péclet number (Pe) defined for one isolated particle as the ratio between hydrodynamic energy and Brownian thermal energy. The measured orientational fields were then directly compared to those obtained for infinitely thin disks through a numerical computation of the Fokker-Plank equation. Even in cases where multiple hydrodynamic interactions dominate, qualitative agreement between both orientational fields is observed, especially at high Péclet number. We have then used an effective approach to assess the viscosity of these suspensions through the definition of an effective volume fraction. Using such an approach, we have been able to transform the relationship between viscosity and volume fraction (ηr = f(φ)) into a relationship that links viscosity with both flow and volume fraction (ηr = f(φ, Pe)).

Preparation and evaluation of tilmicosin-loaded hydrogenated castor oil nanoparticle suspensions of different particle sizes.

Science.gov (United States)

Chen, Xiaojin; Wang, Ting; Lu, Mengmeng; Zhu, Luyan; Wang, Yan; Zhou, WenZhong

2014-01-01

Three tilmicosin-loaded hydrogenated castor oil nanoparticle (TMS-HCO-NP) suspensions of different particle sizes were prepared with different polyvinyl alcohol surfactant concentrations using a hot homogenization and ultrasonic technique. The in vitro release, in vitro antibacterial activity, mammalian cytotoxicity, acute toxicity in mice, and stability study were conducted to evaluate the characteristics of the suspensions. The in vitro tilmicosin release rate, antibacterial activity, mammalian cytotoxicity, acute toxicity in mice, and stability of the suspensions were evaluated. When prepared with polyvinyl alcohol concentrations of 0.2%, 1%, and 5%, the mean diameters of the nanoparticles in the three suspensions were 920±35 nm, 452±10 nm, and 151±4 nm, respectively. The three suspensions displayed biphasic release profiles similar to that of freeze-dried TMS-HCO-NP powders, with the exception of having a faster initial release. Moreover, suspensions of smaller-sized particles showed faster initial release, and lower minimum inhibitory concentrations and minimum bactericidal concentrations. Time-kill curves showed that within 12 hours, the suspension with the 151 nm particles had the most potent bactericidal activity, but later, the suspensions with larger-sized particles showed increased antibacterial activity. None of the three suspensions were cytotoxic at clinical dosage levels. At higher drug concentrations, all three suspensions showed similar concentration-dependent cytotoxicity. The suspension with the smallest-sized particle showed significantly more acute toxicity in mice, perhaps due to faster drug release. All three suspensions exhibited good stability at 4°C and at room temperature for at least 6 months. These results demonstrate that TMS-HCO-NP suspensions can be a promising formulation for tilmicosin, and that nanoparticle size can be an important consideration for formulation development.

Laser induced breakdown detection for the assessment of colloid mediated radionuclide migration