Cell-compatible conducting polyaniline films prepared in colloidal dispersion mode

Czech Academy of Sciences Publication Activity Database

Kašpárková, V.; Humpolíček, P.; Capáková, Z.; Bober, Patrycja; Stejskal, Jaroslav; Trchová, Miroslava; Rejmontová, P.; Junkar, I.; Lehocký, M.; Mozetič, M.

2017-01-01

Roč. 157, 1 September (2017), s. 309-316 ISSN 0927-7765 R&D Projects: GA ČR(CZ) GA17-05095S Institutional support: RVO:61389013 Keywords : polyaniline * conducting films * colloidal dispersions Subject RIV: CD - Macromolecular Chemistry OBOR OECD: Polymer science Impact factor: 3.887, year: 2016

Magnetorheology of colloidal dispersion containing Fe nanoparticles synthesized by the arc-plasma method

International Nuclear Information System (INIS)

Noma, Junichi; Abe, Hiroya; Kikuchi, Takehito; Furusho, Junji; Naito, Makio

2010-01-01

Spherical crystalline Fe nanoparticles, ∼100 nm in diameter, were synthesized under Ar-50% H 2 arc-plasma. These nanoparticles were dispersed in silicone oil after silane treatment on as-grown thin oxide layer (∼2 nm) to make their surfaces hydrophobic. The resulting Fe nanoparticles exhibited a high saturation magnetization of ∼190 emu/g at room temperature. The static magnetorheological behavior was measured for the colloidal dispersion (solid concentration: 15 vol%) at room temperature under magnetic flux densities of 0-0.3 T, using a parallel-plate-type commercial rheometer. The yield stress continuously increased with magnetic flux density, demonstrating the Bingham plastic behavior. Moreover, subjecting the sample to a magnetic flux density of 0.3 T increased the yield stress by ∼10 2 . Additionally, the colloidal dispersion exhibited good stability against sedimentation.

Magnetorheology of colloidal dispersion containing Fe nanoparticles synthesized by the arc-plasma method

Science.gov (United States)

Noma, Junichi; Abe, Hiroya; Kikuchi, Takehito; Furusho, Junji; Naito, Makio

2010-07-01

Spherical crystalline Fe nanoparticles, ˜100 nm in diameter, were synthesized under Ar-50% H 2 arc-plasma. These nanoparticles were dispersed in silicone oil after silane treatment on as-grown thin oxide layer (˜2 nm) to make their surfaces hydrophobic. The resulting Fe nanoparticles exhibited a high saturation magnetization of ˜190 emu/g at room temperature. The static magnetorheological behavior was measured for the colloidal dispersion (solid concentration: 15 vol%) at room temperature under magnetic flux densities of 0-0.3 T, using a parallel-plate-type commercial rheometer. The yield stress continuously increased with magnetic flux density, demonstrating the Bingham plastic behavior. Moreover, subjecting the sample to a magnetic flux density of 0.3 T increased the yield stress by ˜10 2. Additionally, the colloidal dispersion exhibited good stability against sedimentation.

Stereolithographic processing of ceramics: Photon diffusion in colloidal dispersion

Science.gov (United States)

Garg, Rajeev

The technique of ceramic stereolithography (CSL) has been developed for fabricating near net shape ceramic objects. In stereolithography, the three-dimensional computer design file of the object is sliced into thin layers. Each layer is physically fabricated by photocuring the surface of a liquid photo-polymerizable resin bath by raster scanning an ultra-violet laser across the surface of the resin. In CSL, the liquid resin is a high concentration colloidal dispersion in a solution of ultraviolet curable polymers. The ceramic green body fabricated by ceramic stereolithography technique is subjected to the post processing steps of drying, binder burnout and sintering to form a dense ceramic object. An aqueous alumina dispersion in photocuring polymers with particle volume fraction greater than 0.5 was formulated for CSL process. Low molecular weight solution polymers were found to be best suited for formulating ceramic resins due to their inherently low viscosity and favorable interactions with the ceramic dispersant. A hydroxyapatite ceramic resin was also developed for the use in the CSL technique. A model is developed to describe the photocuring process in concentrated ceramic dispersion. The curing profile in ceramic dispersion is governed by multiple scattering from the ceramic particles and absorption by the photocuring polymers. Diffusion theory of light transport is used to model the multiple scattering and absorption phenomena. It is found that diffusive transport adequately describes the phenomena of laser pulse propagation in highly concentrated colloidal dispersions. A model was developed to describe the absorption in highly concentrated ceramic dispersion. Various complex-shaped monolithic alumina and hydroxyapatite objects were fabricated by CSL and shown to possess uniform microstructure. The mechanical properties and sintering behavior of the parts fabricated by CSL are shown to be comparable to those fabricated by other ceramic processing technique

Dynamics of polyelectrolyte adsorption and colloidal flocculation upon mixing studied using mono-dispersed polystyrene latex particles

NARCIS (Netherlands)

Feng, Lili; Cohen Stuart, Martien; Adachi, Yasuhisa

2015-01-01

The dynamic behavior of polyelectrolytes just after their encounter with the surface of bare colloidal particles is analyzed, using the flocculation properties of mono-dispersed polystyrene latex (PSL) particles. Applying a Standardized Colloid Mixing (SCM) approach, effects of ionic strength and

Arsenic speciation in the dispersible colloidal fraction of soils from a mine-impacted creek

International Nuclear Information System (INIS)

Serrano, Susana; Gomez-Gonzalez, Miguel Angel; O’Day, Peggy A.; Laborda, Francisco; Bolea, Eduardo; Garrido, Fernando

2015-01-01

Highlights: • Nanoparticle scorodite may dissolve from mine wastes and release As down-gradient. • Large fractions of total As in soils may be associated with dispersible colloids. • Up to one third of total As in soils was associated with the colloid fraction. • AsFlFFF-ICP-MS and XAS provides information on the partitioning of contaminants in colloids. - Abstract: Arsenic and iron speciation in the dispersible colloid fraction (DCF; 10–1000 nm) from an As-rich mine waste pile, sediments of a streambed that collects runoff from waste pile, the streambed subsoil, and the sediments of a downstream pond were investigated by combining asymmetrical-flow field-flow fractionation (AsFlFFF)/inductively-coupled plasma–mass spectrometry (ICP–MS), transmission electron microscopy (TEM) and X-ray absorption (XAS) spectroscopy. Calcium, Fe and As (Fe/As molar ratio ∼ 1) were the main components of the DCF from waste pile. TEM/EDS and As and Fe XAS analysis revealed the presence of nanoparticle scorodite in this same DCF, as well as Fe nanoparticles in all samples downstream of the waste pile. Arsenic and Fe XAS showed As(V) adsorbed onto nanoparticulate ferrihydrite in the DCF of downstream samples. Micro-X-ray fluorescence indicated a strong correlation between Fe and As in phyllosilicate/Fe 3+ (oxi) hydroxide aggregates from the sediment pond. Fractionation analysis showed the mean particle size of the DCF from the streambed sample to be smaller than that of the streambed subsoil and sediment ponds samples. These results show that an important and variable fraction of As may be bound to dispersible colloids that can be released from contaminated soils and transported downstream in natural systems

Arsenic speciation in the dispersible colloidal fraction of soils from a mine-impacted creek

Energy Technology Data Exchange (ETDEWEB)

Serrano, Susana [Institute of Agrochemistry and Food Technology, CSIC, Agustín Escardino 7, 46980 Paterna, Valencia (Spain); Gomez-Gonzalez, Miguel Angel [National Museum of Natural Sciences, CSIC, José Gutiérrez Abascal 2, 28006 Madrid (Spain); O’Day, Peggy A. [School of Natural Sciences,University of California, Merced, CA 95343 (United States); Laborda, Francisco; Bolea, Eduardo [Group of Analytical Spectroscopy and Sensors (GEAS), Institute of Environmental Sciences (IUCA), University of Zaragoza, Pedro Cerbuna 12, 50009 Zaragoza (Spain); Garrido, Fernando, E-mail: fernando.garrido@mncn.csic.es [National Museum of Natural Sciences, CSIC, José Gutiérrez Abascal 2, 28006 Madrid (Spain)

2015-04-09

Highlights: • Nanoparticle scorodite may dissolve from mine wastes and release As down-gradient. • Large fractions of total As in soils may be associated with dispersible colloids. • Up to one third of total As in soils was associated with the colloid fraction. • AsFlFFF-ICP-MS and XAS provides information on the partitioning of contaminants in colloids. - Abstract: Arsenic and iron speciation in the dispersible colloid fraction (DCF; 10–1000 nm) from an As-rich mine waste pile, sediments of a streambed that collects runoff from waste pile, the streambed subsoil, and the sediments of a downstream pond were investigated by combining asymmetrical-flow field-flow fractionation (AsFlFFF)/inductively-coupled plasma–mass spectrometry (ICP–MS), transmission electron microscopy (TEM) and X-ray absorption (XAS) spectroscopy. Calcium, Fe and As (Fe/As molar ratio ∼ 1) were the main components of the DCF from waste pile. TEM/EDS and As and Fe XAS analysis revealed the presence of nanoparticle scorodite in this same DCF, as well as Fe nanoparticles in all samples downstream of the waste pile. Arsenic and Fe XAS showed As(V) adsorbed onto nanoparticulate ferrihydrite in the DCF of downstream samples. Micro-X-ray fluorescence indicated a strong correlation between Fe and As in phyllosilicate/Fe{sup 3+} (oxi) hydroxide aggregates from the sediment pond. Fractionation analysis showed the mean particle size of the DCF from the streambed sample to be smaller than that of the streambed subsoil and sediment ponds samples. These results show that an important and variable fraction of As may be bound to dispersible colloids that can be released from contaminated soils and transported downstream in natural systems.

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

Liquid-liquid and liquid-solid phase separation and flocculation for a charged colloidal dispersion

International Nuclear Information System (INIS)

Lai, S.K.; Wu, K.L.

2002-01-01

We model the intercolloidal interaction by a hard-sphere Yukawa repulsion to which is added the long-range van der Waals attraction. In comparison with the Derjaguin-Landau-Verwey-Overbeek repulsion, the Yukawa repulsion explicitly incorporates the spatial correlations between colloids and small ions. As a result, the repulsive part can be expressed analytically and has a coupling strength depending on the colloidal volume fraction. By use of this two-body potential of mean force and in conjunction with a second-order thermodynamic perturbation theory, we construct the colloidal Helmholtz free energy and use it to calculate the thermodynamic quantities, pressure and chemical potential, needed in the determination of the liquid-liquid and liquid-solid phase diagrams. We examine, in an aqueous charged colloidal dispersion, the effects of the Hamaker constant and particle size on the conformation of a stable liquid-liquid phase transition calculated with respect to the liquid-solid coexistence phases. We find that there exists a threshold Hamaker constant or particle size whose value demarcates the stable liquid-liquid coexistence phases from their metastable counterparts. Applying the same technique and using the energetic criterion, we extend our calculations to study the flocculation phenomenon in aqueous charged colloids. Here, we pay due attention to determining the loci of a stability curve stipulated for a given temperature T 0 , and obtain the parametric phase diagram of the Hamaker constant vs the coupling strength or, at given surface potential, the particle size. By imposing T 0 to be the critical temperature T c , i.e., setting k B T 0 (=k B T c ) equal to a reasonable potential barrier, we arrive at the stability curve that marks the irreversible reversible phase transition. The interesting result is that there occurs a minimum size for the colloidal particles below (above) which the colloidal dispersion is driven to an irreversible (reversible) phase

Organic-inorganic nanocomposite films made from polyurethane dispersions and colloidal silica particles

Czech Academy of Sciences Publication Activity Database

Serkis, Magdalena; Špírková, Milena; Kredatusová, Jana; Hodan, Jiří; Bureš, R.

2016-01-01

Roč. 23, č. 2 (2016), s. 157-173 ISSN 0927-6440 R&D Projects: GA ČR(CZ) GA13-06700S Institutional support: RVO:61389013 Keywords : polyurethane dispersion * colloidal silica * composites Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.083, year: 2016

Hierarchical opal grating films prepared by slide coating of colloidal dispersions in binary liquid media.

Science.gov (United States)

Lee, Wonmok; Kim, Seulgi; Kim, Seulki; Kim, Jin-Ho; Lee, Hyunjung

2015-02-15

There are active researches on well ordered opal films due to their possible applications to various photonic devices. A recently developed slide coating method is capable of rapid fabrication of large area opal films from aqueous colloidal dispersion. In the current study, the slide coating of polystyrene colloidal dispersions in water/i-propanol (IPA) binary media is investigated. Under high IPA content in a dispersing medium, resulting opal film showed a deterioration of long range order, as well as a decreased film thickness due to dilution effect. From the binary liquid, the dried opal films exhibited the unprecedented topological groove patterns with varying periodic distances as a function of alcohol contents in the media. The groove patterns were consisted of the hierarchical structures of the terraced opal layers with periodic thickness variations. The origin of the groove patterns was attributed to a shear-induced periodic instability of colloidal concentration within a thin channel during the coating process which was directly converted to a groove patterns in a resulting opal film due to rapid evaporation of liquid. The groove periods of opal films were in the range of 50-500 μm, and the thickness differences between peak and valley of the groove were significantly large enough to be optically distinguishable, such that the coated films can be utilized as the optical grating film to disperse infra-red light. Utilizing a lowered hydrophilicity of water/IPA dispersant, an opal film could be successfully coated on a flexible Mylar film without significant dewetting problem. Copyright © 2014 Elsevier Inc. All rights reserved.

Antimicrobial polyethyleneimine-silver nanoparticles in a stable colloidal dispersion.

Science.gov (United States)

Lee, Hyun Ju; Lee, Se Guen; Oh, Eun Jung; Chung, Ho Yun; Han, Sang Ik; Kim, Eun Jung; Seo, Song Yi; Ghim, Han Do; Yeum, Jeong Hyun; Choi, Jin Hyun

2011-11-01

Excellent colloidal stability and antimicrobial activity are important parameters for silver nanoparticles (AgNPs) in a range of biomedical applications. In this study, polyethyleneimine (PEI)-capped silver nanoparticles (PEI-AgNPs) were synthesized in the presence of sodium borohydride (NaBH(4)) and PEI at room temperature. The PEI-AgNPs had a positive zeta potential of approximately +49 mV, and formed a stable nanocolloid against agglomeration due to electrostatic repulsion. The particle size and hydrodynamic cluster size showed significant correlations with the amount of PEI and NaBH(4). PEI-AgNPs and even PEI showed excellent antimicrobial activity against Staphylococus aureus and Klebsiella pneumoniae. The cytotoxic effects of PEI and PEI-AgNPs were confirmed by an evaluation of the cell viability. The results suggest that the amount of PEI should be minimized to the level that maintains the stability of PEI-AgNPs in a colloidal dispersion. Copyright © 2011 Elsevier B.V. All rights reserved.

Dispersions of attractive semiflexible fiberlike colloidal particles from bacterial cellulose microfibrils.

Science.gov (United States)

Kuijk, Anke; Koppert, Remco; Versluis, Peter; van Dalen, Gerard; Remijn, Caroline; Hazekamp, Johan; Nijsse, Jaap; Velikov, Krassimir P

2013-11-26

We prepared dispersions from bacterial cellulose microfibrils (CMF) of a commercial Nata de Coco source. We used an ultra-high-energy mechanical deagglomeration process that is able to disperse the CMFs from the pellicle in which they are organized in an irregular network. Because of the strong attractions between the CMFs, the dispersion remained highly heterogeneous, consisting of fiber bundles, flocs, and voids spanning tens to hundreds of micrometers depending on concentration. The size of these flocs increased with CMF concentration, the size of the bundles stayed constant, and the size of the voids decreased. The observed percolation threshold in MFC dispersions is lower than the theoretical prediction, which is accounted for by the attractive interactions in the system. Because bacterial cellulose is chemically very pure, it can be used to study the interaction of attractive and highly shape-anisotropic, semiflexible fiberlike colloidal particles.

Stability of nano-metric colloidal dispersions of titanium: effect of surface complexation

International Nuclear Information System (INIS)

Peyre, Veronique

1996-01-01

This research thesis reports the study of the adsorption of small organic molecules at the surface of nano-particles of mineral oxides (zirconia), and of its effects on the stability of the colloidal dispersion. Adsorption has been quantified by adsorption isotherms and surface titrations. Processes and mechanisms are thus discussed with respect to pH. The influence of various protecting molecules (acetyl acetone, but also acetic acid, citric acid and diethanolamine) has been studied, and notably highlighted the role of the outer face of the complexing agent in the assessment of reactions between particles which govern the compression and re-dispersability properties of protected dispersions. This study is performed by osmotic pressure measurements and by X-ray diffusion at small angles, completed by statistical mechanics calculations [fr

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

Science.gov (United States)

Lestage, David Jackson

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

Biological properties of printable polyaniline and polyaniline-silver colloidal dispersions stabilized by gelatin

Czech Academy of Sciences Publication Activity Database

Bober, Patrycja; Humpolíček, P.; Syrový, T.; Capáková, Z.; Syrová, L.; Hromádková, Jiřina; Stejskal, Jaroslav

2017-01-01

Roč. 232, October (2017), s. 52-59 ISSN 0379-6779 R&D Projects: GA ČR(CZ) GP14-05568P; GA ČR(CZ) GA17-05095S; GA TA ČR(CZ) TE01020022 Institutional support: RVO:61389013 Keywords : conducting polymer * colloidal dispersion * hybrid composite Subject RIV: CD - Macromolecular Chemistry OBOR OECD: Polymer science Impact factor: 2.435, year: 2016

Colloidal dispersions in external fields: from equilibrium to non-equilibrium

Science.gov (United States)

Lowen, Hartmut

2010-03-01

Dispersions of colloidal particles are excellent model systems of classical statistical mechanics in order to understand the principles of self-organization processes. Using an external field (e.g. electric or magnetic field) the effective interaction between the colloidal particles can be tailored and the system can be brought into non-equilibrium in a controlled way. Glass formation after an ultrafast quench in a two-dimensional superparamagnetic binary colloidal mixture [1,2] will be discussed as well as lane [3,4,5,6,7] and band [8] formation in mixtures of charged suspensions and dusty plasmas driven by an electric field. [4pt] References:[0pt] [1] L. Assoud, F. Ebert, P. Keim, R. Messina, G. Maret, H. Lowen, Phys. Rev. Letters 102, 238301 (2009). [0pt] [2] L. Assoud, F. Ebert, P. Keim, R. Messina, G. Maret, H. Lowen, J. Phys.: Condensed Matter 21, 464114 (2009). [0pt] [3] J. Dzubiella, G. P. Hoffmann, H. Lowen, Phys. Rev. E 65, 021402 (1-8) (2002). [0pt] [4] M. E. Leunissen, C. G. Christova, A. P. Hynninen, C. P. Royall, A. I. Campbell, A. Imhof, M. Dijkstra, R. van Roij, A. van Blaaderen, Nature 437, 235 (2005). [0pt] [5] M. Rex, H. Lowen, Phys. Rev. E 75, 051402 (2007). [0pt] [6] M. Rex, C. P. Royall, A. van Blaaderen, H. Lowen, Lane formation in driven colloidal mixtures: is it continuous or discontinuous?, http://arxiv.org/abs/0812.0908 [0pt] [7] K. R. Sutterlin, A. Wysocki, A. V. Ivlev, C. Rath, H. M. Thomas, M. Rubin-Zuzic, W. J. Goedheer, V. E. Fortov, A. M. Lipaev, V. I. Molotkov, O. F. Petrov, G. E. Morfill, H. Lowen, Phys. Rev. Letters 102, 085003 (2009). [0pt] [8] A. Wysocki, H. Lowen, Phys. Rev. E 79, 041408 (2009).

On the effects from the simultaneous occurrence of the critical Casimir and dispersion forces between conical colloid particle and a thick plate immersed in nonpolar critical fluid

Directory of Open Access Journals (Sweden)

Valchev Galin

2018-01-01

Full Text Available Here we study the interplay between the van der Waals (vdWF and critical Casimir forces (CCF, as well as the total force (TF between a conical colloid particle and a thick planar slab. We do that using general scaling arguments and mean-field type calculations utilizing the so-called “surface integration approach”, a generalization of the well known Derjaguin approximation. Its usage in the present research, requires knowledge on the forces between two parallel slabs, confining in between some fluctuating fluid medium characterized by its temperature T and chemical potential μ. The surfaces of the colloid particle and the slab are assumed coated by thin layers exerting strong preference to the liquid phase of a simple fluid, or one of the components of a binary mixture, modeled by strong adsorbing local surface potentials, ensuring the so-called (+,+ boundary conditions. On the other hand, the core region of the slab and the particle, influence the fluid by long-ranged competing dispersion potentials. We demonstrate that for a suitable set of colloid-fluid, slab-fluid, and fluid-fluid coupling parameters the competition between the effects due to the coatings and the core regions of the objects, result, when one changes T or μ, in sign change of the Casimir force (CF and the TF acting between the colloid and the slab. Such an effect can provide a strategy for solving problems with handling, feeding, trapping and fixing of microparts in nanotechnology.

Analysis of colloid transport

International Nuclear Information System (INIS)

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

1985-01-01

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

Low molecular weight compounds as effective dispersing agents in the formation of colloidal silver nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Natsuki, Jun; Natsuki, Toshiaki, E-mail: natsuki@shinshu-u.ac.jp; Abe, Takao [Shinshu University, Faculty of Textile Science and Technology (Japan)

2013-03-15

A convenient method to synthesize uniform, well-dispersed colloidal silver nanoparticles is described. Aldonic acid or {alpha}-hydroxy acid compounds of low molecular weight are used instead of polymeric compounds as dispersing agents to prepare silver nanoparticles. The size, conformation, and electrical conductivity of the silver nanoparticles, and the effect and function of the dispersing agents are investigated in detail. Using these low molecular weight compounds as dispersing agents, silver nanoparticles with a diameter of 10 nm or less and high electrical conductivity can be obtained. In addition, this procedure allows silver nanoparticles to be sintered at 150 Degree-Sign C, which is lower than that required for silver nanoparticle formulation using polymeric compounds (200 Degree-Sign C). The silver nanoparticles produced by this process can be used to prepare various inks and to manufacture electronic circuits. It is found that low molecular weight compounds are more effective dispersing agents than polymeric compounds in the formation of silver nanoparticles.

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

International Nuclear Information System (INIS)

Snezhko, Alexey

2011-01-01

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

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

Colloidal phytosterols: synthesis, characterization and bioaccessibility

NARCIS (Netherlands)

Rossi, L.; Seijen ten Hoorn, J.W.M.; Melnikov, S.M.; Velikov, K.P.

2010-01-01

We demonstrate the synthesis of phytosterol colloidal particles using a simple food grade method based on antisolvent precipitation in the presence of a non-ionic surfactant. The resulting colloidal particles have a rod-like shape with some degree of crystallinity. The colloidal dispersions display

Polymers at interfaces and in colloidal dispersions.

Science.gov (United States)

Fleer, Gerard J

2010-09-15

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

Lanthanide Phytanates: Liquid-Crystalline Phase Behavior, Colloidal Particle Dispersions, and Potential as Medical Imaging Agents

Energy Technology Data Exchange (ETDEWEB)

Conn, Charlotte E.; Panchagnula, Venkateswarlu; Weerawardena, Asoka; Waddington, Lynne J.; Kennedy, Danielle F.; Drummond, Calum J. (CSIRO/MHT); (CSIRO/MSE)

2010-08-23

Lanthanide salts of phytanic acid, an isoprenoid-type amphiphile, have been synthesized and characterized. Elemental analysis and FTIR spectroscopy were used to confirm the formed product and showed that three phytanate anions are complexed with one lanthanide cation. The physicochemical properties of the lanthanide phytanates were investigated using DSC, XRD, SAXS, and cross-polarized optical microscopy. Several of the hydrated salts form a liquid-crystalline hexagonal columnar mesophase at room temperature, and samarium(III) phytanate forms this phase even in the absence of water. Select lanthanide phytanates were dispersed in water, and cryo-TEM images indicate that some structure has been retained in the dispersed phase. NMR relaxivity measurements were conducted on these systems. It has been shown that a particulate dispersion of gadolinium(III) phytanate displays proton relaxivity values comparable to those of a commercial contrast agent for magnetic resonance imaging and a colloidal dispersion of europium(III) phytanate exhibits the characteristics of a fluorescence imaging agent.

Lanthanide Phytanates: Liquid-Crystalline Phase Behavior, Colloidal Particle Dispersions, and Potential as Medical Imaging Agents

International Nuclear Information System (INIS)

Conn, Charlotte E.; Panchagnula, Venkateswarlu; Weerawardena, Asoka; Waddington, Lynne J.; Kennedy, Danielle F.; Drummond, Calum J.

2010-01-01

Lanthanide salts of phytanic acid, an isoprenoid-type amphiphile, have been synthesized and characterized. Elemental analysis and FTIR spectroscopy were used to confirm the formed product and showed that three phytanate anions are complexed with one lanthanide cation. The physicochemical properties of the lanthanide phytanates were investigated using DSC, XRD, SAXS, and cross-polarized optical microscopy. Several of the hydrated salts form a liquid-crystalline hexagonal columnar mesophase at room temperature, and samarium(III) phytanate forms this phase even in the absence of water. Select lanthanide phytanates were dispersed in water, and cryo-TEM images indicate that some structure has been retained in the dispersed phase. NMR relaxivity measurements were conducted on these systems. It has been shown that a particulate dispersion of gadolinium(III) phytanate displays proton relaxivity values comparable to those of a commercial contrast agent for magnetic resonance imaging and a colloidal dispersion of europium(III) phytanate exhibits the characteristics of a fluorescence imaging agent.

Self-Assembly of Faceted Colloidal Particles

NARCIS (Netherlands)

Gantapara, A.P.

2015-01-01

A colloidal dispersion consists of insoluble microscopic particles that are suspended in a solvent. Typically, a colloid is a particle for which at least one of its dimension is within the size range of a nanometer to a micron. Due to collisions with much smaller solvent molecules, colloids perform

Stability studies of colloidal silica dispersions in binary solvent mixtures

International Nuclear Information System (INIS)

Bean, Keith Howard

1997-01-01

A series of monodispersed colloidal silica dispersions, of varying radii, has been prepared. These particles are hydrophilic in nature due to the presence of surface silanol groups. Some of the particles have been rendered hydrophobic by terminally grafting n-alkyl (C 18 ) chains to the surface. The stability of dispersions of these various particles has been studied in binary mixtures of liquids, namely (i) ethanol and cyclohexane, and (ii) benzene and n-heptane. The ethanol - cyclohexane systems have been studied using a variety of techniques. Adsorption excess isotherms have been established and electrophoretic mobility measurements have been made. The predicted stability of the dispersions from D.V.L.O. calculations is compared to the observed stability. The hydrophilic silica particles behave as predicted by the calculations, with the zeta potential decreasing and the van der Waals attraction increasing with increasing cyclohexane concentration. The hydrophobic particles behave differently than expected, and the stability as a function of solvent mixture composition does not show a uniform trend. The effect of varying the coverage of C 18 chains on the surface and the effect of trace water in the systems has also been investigated. Organophilic silica dispersions in benzene - n-heptane solvent mixtures show weak aggregation and phase separation into a diffuse 'gas-like' phase and a more concentrated 'liquid-like' phase, analogous to molecular condensation processes. Calculations of the van der Waals potential as a function of solvent mixture composition show good agreement with the observed stability. Determination of the number of particles in each phase at equilibrium allows the energy of flocculation to be determined using a simple thermodynamic relationship. Finally, the addition of an AB block copolymer to organophilic silica particles in benzene n-heptane solvent mixtures has been shown to have a marked effect on the dispersion stability. This stability

Clustering and self-assembly in colloidal systems

NARCIS (Netherlands)

Smallenburg, F.

2012-01-01

A colloidal dispersion consists of small particles called colloids, typically tens of nanometers to a few micrometers in size, suspended in a solvent. Due to collisions with the much smaller particles in the solvent, colloids perform Brownian motion: randomly directed movements that cause the

Superhydrophilic graphite surfaces and water-dispersible graphite colloids by electrochemical exfoliation

Energy Technology Data Exchange (ETDEWEB)

Li, Yueh-Feng [Department of Chemical and Materials Engineering, National Central University, Jhongli, 320 Taiwan (China); Chen, Shih-Ming; Lai, Wei-Hao [Materials and Chemical Research Laboratories, Industrial Technology Research Institute, Chutung, Hsinchu, 31040 Taiwan (China); Sheng, Yu-Jane [Department of Chemical Engineering, National Taiwan University, Taipei, 106 Taiwan (China); Tsao, Heng-Kwong [Department of Chemical and Materials Engineering, Department of Physics, National Central University, Jhongli, 320 Taiwan (China)

2013-08-14

Superhydrophilic graphite surfaces and water-dispersible graphite colloids are obtained by electrochemical exfoliation with hydrophobic graphite electrodes. Such counterintuitive characteristics are caused by partial oxidation and investigated by examining both graphite electrodes and exfoliated particles after electrolysis. The extent of surface oxidation can be explored through contact angle measurement, scanning electron microscope, electrical sheet resistance, x-ray photoelectron spectroscopy, zeta-potential analyzer, thermogravimetric analysis, UV-visible, and Raman spectroscopy. The degree of wettability of the graphite anode can be altered by the electrolytic current and time. The water contact angle declines generally with increasing the electrolytic current or time. After a sufficient time, the graphite anode becomes superhydrophilic and its hydrophobicity can be recovered by peeling with adhesive tape. This consequence reveals that the anodic graphite is oxidized by oxygen bubbles but the oxidation just occurs at the outer layers of the graphite sheet. Moreover, the characteristics of oxidation revealed by UV peak shift, peak ratio between D and G bands, and negative zeta-potential indicate the presence of graphite oxide on the outer shell of the exfoliated colloids. However, thermogravimetric analysis for the extent of decomposition of oxygen functional groups verifies that the amount of oxygen groups is significantly less than that of graphite oxide prepared via Hummer method. The structure of this partially oxidized graphite may consist of a graphite core covered with an oxidized shell. The properties of the exfoliated colloids are also influenced by pH of the electrolytic solution. As pH is increased, the extent of oxidation descends and the thickness of oxidized shell decreases. Those results reveal that the degree of oxidation of exfoliated nanoparticles can be manipulated simply by controlling pH.

Density fluctuation in a screened Coulombic colloid dispersion: comparison of the liquid and cubic phases of lipid A-diphosphate

International Nuclear Information System (INIS)

Brown, Helen; Ross, D. Keith; Paradies, Henrich H.

2004-01-01

Light-, small-angle X-ray and neutron scattering measurements of the dynamic structure factor S(Q,t) of strong interacting dispersions of lipid A-diphosphate were recorded and analysed applying existing models of liquid state theory. Lipid A-diphosphate ordering was observed at low volume fractions (phi=2.2x10 -4 ) and at very low ionic strength (I=10 -5 M). Upon increasing the particle number density of lipid A-diphosphate a transformation of the lattices of the colloidal crystals from a BCC lattice (a=36.20 nm) to a FCC lattice (a=57.30 nm) occurred. This strongly suggests a similarity in the preformed liquid structure and the cubic colloidal phase. The fit of both S eff (Q) and the principle peak I p (Q) with the effective particle charge supports of the main conclusions drawn from the SANS experiments and the liquid state theory indicating the presence of long-range order for the dispersions of lipid A-diphosphate

Colloidal dispersions of maghemite nanoparticles produced by laser pyrolysis with application as NMR contrast agents

Energy Technology Data Exchange (ETDEWEB)

Veintemillas-Verdaguer, Sabino [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049 Madrid (Spain); Morales, Maria del Puerto [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049 Madrid (Spain); Bomati-Miguel, Oscar [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049 Madrid (Spain); Bautista, Carmen [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049 Madrid (Spain); Zhao, Xinqing [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049 Madrid (Spain); Bonville, Pierre [CEA, CE Saclay, DSM/DRECAM/SPEC, 91191 Gif-Sur-Yvette (France); Alejo, Rigoberto Perez de [Universidad Complutense de Madrid, Unidad de RMN, Paseo Juan XXIII, 1, 28040 Madrid (Spain); Ruiz-Cabello, Jesus [Universidad Complutense de Madrid, Unidad de RMN, Paseo Juan XXIII, 1, 28040 Madrid (Spain); Santos, Martin [Hospital Universitario Puerta de Hierro, Servicio de Cirugia Experimental. C/San Martin de Porres 4, 28035 Madrid (Spain); Tendillo-Cortijo, Francisco J [Hospital Universitario Puerta de Hierro, Servicio de Cirugia Experimental. C/San Martin de Porres 4, 28035 Madrid (Spain); Ferreiros, Joaquin [Hospital Clinico de Madrid ' San Carlos' , Ciudad Universitaria, 28040 Madrid (Spain)

2004-08-07

Biocompatible magnetic dispersions have been prepared from {gamma}-Fe{sub 2}O{sub 3} nanoparticles (5 nm) synthesized by continuous laser pyrolysis of Fe(CO){sub 5} vapours. The feasibility of using these dispersions as magnetic resonance imaging (MRI) contrast agents has been analysed in terms of chemical structure, magnetic properties, {sup 1}H NMR relaxation times and biokinetics. The magnetic nanoparticles were dispersed in a strong alkaline solution in the presence of dextran, yielding stable colloids in a single step. The dispersions consist of particle-aggregates 25 nm in diameter measured using transmission electron microscope and a hydrodynamic diameter of 42 nm measured using photon correlation spectroscopy. The magnetic and relaxometric properties of the dispersions were of the same order of magnitude as those of commercial contrast agents produced using coprecipitation. However, these dispersions, when injected intravenously in rats at standard doses showed a mono-exponential blood clearance instead of a biexponential one, with a blood half-life of 7 {+-} 1 min. Furthermore, an important enhancement of the image contrast was observed after the injection, mainly located at the liver and the spleen of the rat. In conclusion, the laser pyrolysis technique seems to be a good alternative to the coprecipitation method for producing MRI contrast agents, with the advantage of being a continuous synthesis method that leads to very uniform particles capable of being dispersed and therefore transformed in a biocompatible magnetic liquid.

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

Evolution of colloidal dispersions in novel time-varying optical potentials

Science.gov (United States)

Koss, Brian Alan

Optical traps use forces exerted by a tightly focused light beam to trap objects from tens of nanometers to tens of micrometers in size. Since their introduction in 1986, optical tweezers have become very useful to biology, chemistry, and soft condensed-matter physics. Work presented here, promises to advance optical tweezers not only in fundamental scientific research, but also in applications outside of the laboratory and into the mainstream of miniaturized manufacturing and diagnostics. By providing unprecedented access to the mesoscopic world, a new generation of optical traps, called Dynamic Holographic Optical Tweezers (HOTs) offers revolutionary new opportunities for fundamental and applied research. To demonstrate this technique, HOTs will be used to pump particles via a new method of transport called Optical Peristalsis (OP). OP is efficient method for transporting mesoscopic objects in three dimensions using short repetitive sequences of holographic optical trapping patterns. Transport in this process is analogous to peristaltic pumping, with the configurations of optical traps mimicking states of a peristaltic pump. While not limited to the deterministic particle transport, OP, can also be a platform to investigate the stochastic limit of particle transport. Advances in recent years have demonstrated that a variety of time-varying perturbations can induce drift in a diffusive system without exerting an overall force. Among these, are thermal ratchet models in which the system is subjected to time-varying energy landscapes that break spatiotemporal symmetry and thereby induce drift. Typically, the potential energy landscape is chosen to be the sawtooth potential. This work describes an alternate class of symmetric thermal ratchet models, that are not sawtooth, and demonstrates their efficacy in biasing the diffusion of colloidal spheres in both the stochastic and deterministic limits. Unlike previous models, each state in this thermal ratchet consists of

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

Wetting in a colloidal liquid-gas system

NARCIS (Netherlands)

Wijting, W.K.; Besseling, N.A.M.; Cohen Stuart, M.A.

2003-01-01

We present first observations of wetting phenomena in depletion interaction driven, phase separated colloidal dispersions (coated silica-cyclohexane-polydimethylsiloxane). The contact angle of the colloidal liquid-gas interface at a solid substrate (coated glass) was determined for a series of

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.

Colloidal nematostatics

Directory of Open Access Journals (Sweden)

V.M. Pergamenshchik

2010-01-01

Full Text Available We give a review of the theory of large distance colloidal interaction via the nematic director field. The new area of nematic colloidal systems (or nematic emulsions has been guided by the analogy between the colloidal nematostatics and electrostatics. The elastic charge density representation of the colloidal nematostatics [V.M. Pergamenshchik, V.O. Uzunova, Eur. Phys. J. E, 2007, 23, 161; Phys. Rev. E, 2007, 76, 011707] develops this analogy at the level of charge density and Coulomb interaction. The analogy is shown to lie in common mathematics based on the solutions of Laplace equation. However, the 3d colloidal nematostatics substantially differs from electrostatics both in its mathematical structure and physical implications. The elastic charge is a vector fully determined by the torque exerted upon colloid, the role of Gauss' theorem is played by conservation of the torque components. Elastic multipoles consist of two tensors (dyads. Formulas for the elastic multipoles, the Coulomb-like, dipole-dipole, and quadrupole-quadrupole pair interaction potentials are derived and illustrated by particular examples. Based on the tensorial structure, we list possible types of elastic dipoles and quadrupoles. An elastic dipole is characterized by its isotropic strength, anisotropy, chirality, and its longitudinal component. An elastic quadrupole can be uniaxial and biaxial. Relation between the multipole type and its symmetry is discussed, sketches of some types of multipoles are given. Using the mirror image method of electrostatics as a guiding idea, we develop the mirror image method in nematostatics for arbitrary director tilt at the wall. The method is applied to the charge-wall and dipole-wall interaction.

Non-iridescent structural colors from uniform-sized SiO2 colloids

Science.gov (United States)

Topçu, Gökhan; Güner, Tuğrul; Demir, Mustafa M.

2018-05-01

Structural colors have recently attracted interest from diverse fields of research due to their ease of fabrication and eco-friendliness. These types of colors are, in principle, achieved by periodically arranged submicron-diameter colloidal particles. The interaction of light with a structure containing long-range ordered colloidal particles leads to coloration; this usually varies depending on the angle of observation (iridescence). However, the majority of the applications demand constant color that is independent of the viewing angle (non-iridescence). In this work, silica colloids were obtained using the Stöber method at different sizes from 150 to 300 nm in an alcoholic dispersion. The casting of the dispersion on a substrate leaves behind a photonic crystal showing a colorful iridescent film. However, centrifugation and redispersion of the SiO2 particles into fresh solvent may cause the formation of small, aggregated silica domains in the new dispersion. The casting of this dispersion allows for the development of photonic glass, presumably due to the accumulation of aggregates showing stable colloidal film independent of viewing angle. Moreover, depending on the size of the silica colloids, non-iridescent photonic glasses with various colors (violet, blue, green, and orange) are obtained.

Colloid Release from Soil Aggregates

DEFF Research Database (Denmark)

Vendelboe, Anders Lindblad; Møldrup, Per; Schjønning, Per

2012-01-01

The content of water-dispersible colloids (WDC) has a major impact on soil functions and structural stability. In addition, the presence of mobile colloids may increase the risk of colloid-facilitated transport of strongly sorbing environmental contaminants. The WDC content was measured in 39 soils......, using laser diffraction, by agitating the samples using a wet-dispersion unit. This approach eliminated the need for long sedimentation times required by the more classical end-over-end shaking approach and provided information about the time-dependent release of WDC. The total clay content of the soils...... ranged from 0.1 to 0.44 kg kg−1. The WDC content was measured on air-dry and moist 1- to 2-mm aggregates. The WDC content at a reference time was highly correlated to the total clay content (r > 0.91, P soils. Only for two sites was the WDC content correlated to the content of clay...

Cell-compatible conducting polyaniline films prepared in colloidal dispersion mode.

Science.gov (United States)

Kašpárková, Věra; Humpolíček, Petr; Capáková, Zdenka; Bober, Patrycja; Stejskal, Jaroslav; Trchová, Miroslava; Rejmontová, Petra; Junkar, Ita; Lehocký, Marián; Mozetič, Miran

2017-09-01

Conducting polyaniline can be prepared and modified using several procedures, all of which can significantly influence its applicability in different fields of biomedicine or biotechnology. The modifications of surface properties are crucial with respect to the possible applications of this polymer in tissue engineering or as biosensors. Innovative technique for preparing polyaniline films via in-situ polymerization in colloidal dispersion mode using four stabilizers (poly-N-vinylpyrrolidone; sodium dodecylsulfate; Tween 20 and Pluronic F108) was developed. The surface energy, conductivity, spectroscopic features, and cell compatibility of thin polyaniline films were determined using contact-angle measurement, the van der Pauw method, Fourier-transform infrared spectroscopy, and assay conducted on mouse fibroblasts, respectively. The stabilizers significantly influenced not only the surface and electrical properties of the films but also their cell compatibility. Sodium dodecylsulfate seems preferentially to combine both the high conductivity and good cell compatibility. Moreover, the films with sodium dodecylsulfate were non-irritant for skin, which was confirmed by their in-vitro exposure to the 3D-reconstructed human tissue model. Copyright © 2017 Elsevier B.V. All rights reserved.

Preparation and dispersive properties of Ag colloid by electrical explosion of wire

International Nuclear Information System (INIS)

Yun, G.S.; Bac, L.H.; Kim, J.S.; Kwon, Y.S.; Choi, H.S.; Kim, J.C.

2011-01-01

Research highlights: → Wire diameter and synthetic temperature affect on properties of Ag colloid by EEW. → The lower temperature and smaller diameter make smaller size and narrower size distribution. → Ag colloid are more stable at lower synthetic temperature and smaller size. - Abstract: In this work, Ag colloid was prepared by electrical explosion of wire in deionized water with 0.2 mm and 0.3 mm wire diameter. The temperature of water used for medium of explosion process was change from 20 deg. C to 80 deg. C. Morphology and particle size of nanoparticles was observed by transmission electron microscope. The particle size and size distribution of nanoparticles was found to shift to a smaller size with a decrease of temperature and smaller wire diameter. Surface plasmon resonance of the silver colloids was studied by UV-vis spectroscopy. Stability of silver colloids was investigated by zeta-potential and Turbiscan techniques. The results indicated that temperature of medium during explosion affects much on the stability of Ag colloid. The silver colloidal stability prepared at lower temperature and smaller wire diameter was more stable.

Amphotericin B colloidal dispersion (Amphocil) vs fluconazole for the prevention of fungal infections in neutropenic patients : data of a prematurely stopped clinical trial

NARCIS (Netherlands)

Timmers, G J; Zweegman, S; Simoons-Smit, A M; van Loenen, A C; Touw, D; Huijgens, P C

We conducted an open label, randomised clinical trial to compare amphotericin B colloidal dispersion (ABCD, Amphocil) 2 mg/kg/day intravenously with fluconazole 200 mg/day orally, for the prevention of fungal disease in neutropenic patients with haematological malignancies. In the event of

Liquid Crystal Phases of Colloidal Platelets and their Use as Nanocomposite Templates

NARCIS (Netherlands)

Mourad, M.C.D.|info:eu-repo/dai/nl/304837563

2009-01-01

This thesis explores the gelation and liquid crystal phase behavior of colloidal dispersions of platelike particles as well as the use of such dispersions for the generation of nanocomposites. We report on the sol-gel, sol-glass and liquid crystal phase transitions of positively charged colloidal

Depletion and the dynamics in colloid-polymer mixtures

NARCIS (Netherlands)

Tuinier, R.; Fan, T.H.; Taniguchi, T.

2015-01-01

The status of work on the influence of nonadsorbing polymers on depletion dynamics in colloidal dispersions is reviewed. In the past focus has been paid to equilibrium properties of colloid-polymer mixtures. In practice the dynamical behaviour is equally important. Dynamic properties including

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.

Wetting in a Colloidal Liquid-Gas System

Science.gov (United States)

Wijting, W. K.; Besseling, N. A.; Stuart, M. A.

2003-05-01

We present first observations of wetting phenomena in depletion interaction driven, phase separated colloidal dispersions (coated silica cyclohexane-polydimethylsiloxane). The contact angle of the colloidal liquid-gas interface at a solid substrate (coated glass) was determined for a series of compositions. Upon approach to the critical point, a transition occurs from partial to complete wetting.

Wetting in a colloidal liquid-gas system

OpenAIRE

Wijting, W.K.; Besseling, N.A.M.; Cohen Stuart, M.A.

2003-01-01

We present first observations of wetting phenomena in depletion interaction driven, phase separated colloidal dispersions (coated silica-cyclohexane-polydimethylsiloxane). The contact angle of the colloidal liquid-gas interface at a solid substrate (coated glass) was determined for a series of compositions. Upon approach to the critical point, a transition occurs from partial to complete wetting.

Glass transition in soft-sphere dispersions

International Nuclear Information System (INIS)

RamIrez-Gonzalez, P E; Medina-Noyola, M

2009-01-01

The concept of dynamic equivalence among mono-disperse soft-sphere fluids is employed in the framework of the self-consistent generalized Langevin equation (SCGLE) theory of colloid dynamics to calculate the ideal glass transition phase diagram of model soft-sphere colloidal dispersions in the softness-concentration state space. The slow dynamics predicted by this theory near the glass transition is compared with available experimental data for the decay of the intermediate scattering function of colloidal dispersions of soft-microgel particles. Increasing deviations from this simple scheme occur for increasingly softer potentials, and this is studied here using the Rogers-Young static structure factor of the soft-sphere systems as the input of the SCGLE theory, without assuming a priori the validity of the equivalence principle above.

Holographic characterization of colloidal particles in turbid media

Science.gov (United States)

Cheong, Fook Chiong; Kasimbeg, Priya; Ruffner, David B.; Hlaing, Ei Hnin; Blusewicz, Jaroslaw M.; Philips, Laura A.; Grier, David G.

2017-10-01

Holographic particle characterization uses in-line holographic microscopy and the Lorenz-Mie theory of light scattering to measure the diameter and the refractive index of individual colloidal particles in their native dispersions. This wealth of information has proved invaluable in fields as diverse as soft-matter physics, biopharmaceuticals, wastewater management, and food science but so far has been available only for dispersions in transparent media. Here, we demonstrate that holographic characterization can yield precise and accurate results even when the particles of interest are dispersed in turbid media. By elucidating how multiple light scattering contributes to image formation in holographic microscopy, we establish the range conditions under which holographic characterization can reliably probe turbid samples. We validate the technique with measurements on model colloidal spheres dispersed in commercial nanoparticle slurries.

Structure of magnetic particles studied by small angle neutron scattering. [Magnetic colloid particles in stable liquid dispersion

Energy Technology Data Exchange (ETDEWEB)

Cebula, D J; Charles, S W; Popplewell, J

1981-03-01

The purpose of this note is to show how the use of small angle neutron scattering (SANS) can provide fundamental information on the structure of magnetic colloid particles in stable liquid dispersion. A more detailed account elaborating the use of the technique to provide fundamental information on interactions will appear later. This contribution contains some principal results on particle structure. The technique of SANS provides a very sensitive means of measuring particle size by measuring the scattered neutron intensity, I(Q), as a function of scattered wave vector, Q.

Wetting behavior in colloid-polymer mixtures at different substrates

NARCIS (Netherlands)

Wijting, W.K.; Besseling, N.A.M.; Cohen Stuart, M.A.

2003-01-01

We present experimental observations on wetting phenomena in depletion interaction driven, phase separated colloidal dispersions. The contact angle of the colloidal liquid-gas interface at a solid substrate was determined for a series of compositions. Upon approach to the critical point, a

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...

Stabilized super-thermite colloids: A new generation of advanced highly energetic materials

Science.gov (United States)

Elbasuney, Sherif; Gaber Zaky, M.; Radwan, Mostafa; Mostafa, Sherif F.

2017-10-01

One of the great impetus of nanotechnology on energetic materials is the achievement of nanothermites (metal-oxide/metal) which are characterized by massive heat output. Yet, full exploitation of super-thermites in highly energetic systems has not been achieved. This manuscript reports on the sustainable fabrication of colloidal Fe2O3 and CuO nanoparticles for thermite applications. TEM micrographs demonstrated mono-dispersed Fe2O3 and CuO with an average particle size of 3 and 15 nm respectively. XRD diffractograms demonstrated highly crystalline materials. SEM micrographs demonstrated a great tendency of the developed oxides to aggregate over drying process. The effective integration and dispersion of mono-dispersed colloidal thermite particles into energetic systems are vital for enhanced performance. Aluminum is of interest as highly energetic metal fuel. In this paper, synthesized Fe2O3 and CuO nanoparticles were re-dispersed in isopropyl alcohol (IPA) with aluminum nanoparticles using ultrasonic prope homogenizer. The colloidal thermite peraticles can be intgegrated into highly energetic system for subsequent nanocomposite development. Thanks to stabilization of colloidal CuO nanoparticles in IPA which could offer intimate mixing between oxidizer and metal fuel. The stabilization mechanism of CuO in IPA was correlated to steric stabilization with solvent molecules. This approach eliminated nanoparticle drying and the re-dispersion of dry aggregates into energetic materials. This manuscript shaded the light on the real development of colloidal thermite mixtures and their integration into highly energetic systems.

Measurements of dispersion forces between colloidal latex particles with the atomic force microscope and comparison with Lifshitz theory

Energy Technology Data Exchange (ETDEWEB)

Elzbieciak-Wodka, Magdalena; Ruiz-Cabello, F. Javier Montes; Trefalt, Gregor; Maroni, Plinio; Borkovec, Michal, E-mail: michal.borkovec@unige.ch [Department of Inorganic and Analytical Chemistry, University of Geneva, Sciences II, 30, Quai Ernest-Ansermet, 1205 Geneva (Switzerland); Popescu, Mihail N. [Ian Wark Research Institute, University of South Australia, Mawson Lakes, SA 5095 (Australia)

2014-03-14

Interaction forces between carboxylate colloidal latex particles of about 2 μm in diameter immersed in aqueous solutions of monovalent salts were measured with the colloidal probe technique, which is based on the atomic force microscope. We have systematically varied the ionic strength, the type of salt, and also the surface charge densities of the particles through changes in the solution pH. Based on these measurements, we have accurately measured the dispersion forces acting between the particles and estimated the apparent Hamaker constant to be (2.0 ± 0.5) × 10{sup −21} J at a separation distance of about 10 nm. This value is basically independent of the salt concentration and the type of salt. Good agreement with Lifshitz theory is found when roughness effects are taken into account. The combination of retardation and roughness effects reduces the value of the apparent Hamaker constant and its ionic strength dependence with respect to the case of ideally smooth surfaces.

Hydrothermal synthesis of highly water-dispersible anatase nanocrystals from transparent aqueous sols of titanate colloids

International Nuclear Information System (INIS)

Ban, Takayuki; Tanaka, Yusuke; Ohya, Yutaka

2011-01-01

Transparent colloidal aqueous solutions of anatase nanocrystals were hydrothermally synthesized from aqueous transparent sols with tetramethylammonium titanate colloids, the surfaces of which were modified with citric acid, by structural conversion of the titanate to anatase. This modification hindered coalescence of the titanate colloids during the hydrothermal synthesis. Although the amount of citric acid adsorbed on the colloids was reduced during hydrothermal treatment, a small amount of citric acid was adsorbed on the resulting anatase nanocrystals. Moreover, the use of the titanate colloids as a precursor was compared with the use of a citrato Ti complex, tetramethylammonium citratotitanate. The hydrothermal treatment of the transparent aqueous solutions of the Ti complex yielded opaque solutions with large anatase colloids, suggesting that the titanate colloids were useful for preparing transparent anatase colloidal solutions. Because the shape and size of resulting colloids may be dependent on the size and shape of starting colloids, the use of titanate colloids as a precursor may make it easy to control size and shape of anatase colloids.

Particle morphology as a control of permeation in polymer films obtained from MMA/nBA colloidal dispersions.

Science.gov (United States)

Lestage, David J; Urban, Marek W

2004-07-20

The combination of precision-controlled weight loss measurements and spectroscopic surface FT-IR analysis allowed us to identify unique behaviors of poly(methyl methacrylate) (p-MMA). When MMA and n-butyl acrylate (nBA) are polymerized into p-MMA and p-nBA homopolymer blends, MMA/nBA random copolymers, and p-MMA/p-nBA core-shell morphologies, a controlled mobility and stratification of low molecular weight components occurs in films formed from coalesced colloidal dispersions. Due to different affinities toward water, p-MMA and p-nBA are capable of releasing water at different rates, depending upon particle morphological features of initial dispersions. As coalescence progresses, water molecules are released from the high free volume p-nBA particles, whereas p-MMA retains water molecules for the longest time due to its hydrophilic nature. As a result, water losses at extended coalescence times are relatively small for p-MMA. MMA/nBA copolymer and p-MMA/p-nBA blends follow the same trends, although the magnitudes of changes are not as pronounced. The p-MMA/p-nBA core-shell behavior resembles that of p-nBA homopolymer, which is attributed to significantly lower content of the p-MMA component in particles. Annealing of coalesced colloidal films at elevated temperatures causes migration of SDOSS to the F-A interface, but for films containing primarily p-nBA, reverse diffusion back into the bulk is observed. These studies illustrate that the combination of different particle morphologies and temperatures leads to controllable permeation processes through polymeric films. Copyright 2004 American Chemical Society

Colloid transport in saturated porous media: Elimination of attachment efficiency in a new colloid transport model

Science.gov (United States)

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

2013-01-01

A colloid transport model is introduced that is conceptually simple yet captures the essential features of colloid transport and retention in saturated porous media when colloid retention is dominated by the secondary minimum because an electrostatic barrier inhibits substantial deposition in the primary minimum. This model is based on conventional colloid filtration theory (CFT) but eliminates the empirical concept of attachment efficiency. The colloid deposition rate is computed directly from CFT by assuming all predicted interceptions of colloids by collectors result in at least temporary deposition in the secondary minimum. Also, a new paradigm for colloid re-entrainment based on colloid population heterogeneity is introduced. To accomplish this, the initial colloid population is divided into two fractions. One fraction, by virtue of physiochemical characteristics (e.g., size and charge), will always be re-entrained after capture in a secondary minimum. The remaining fraction of colloids, again as a result of physiochemical characteristics, will be retained “irreversibly” when captured by a secondary minimum. Assuming the dispersion coefficient can be estimated from tracer behavior, this model has only two fitting parameters: (1) the fraction of the initial colloid population that will be retained “irreversibly” upon interception by a secondary minimum, and (2) the rate at which reversibly retained colloids leave the secondary minimum. These two parameters were correlated to the depth of the Derjaguin-Landau-Verwey-Overbeek (DLVO) secondary energy minimum and pore-water velocity, two physical forces that influence colloid transport. Given this correlation, the model serves as a heuristic tool for exploring the influence of physical parameters such as surface potential and fluid velocity on colloid transport.

Colloid and phosphorus leaching from undisturbed soil cores sampled along a natural clay gradient

DEFF Research Database (Denmark)

Vendelboe, Anders Lindblad; Møldrup, Per; Heckrath, Goswin Johann

2011-01-01

correlated to the accumulated outflow and was described as a diffusion controlled process, using ¾(accumulated outflow). The mass of leached particles was positively correlated to the clay content as well as to water-dispersible colloids. Particulate phosphorus (P) was linearly correlated to concentration......The presence of strongly sorbing compounds in groundwater and tile drains can be a result of colloid-facilitated transport. Colloid and phosphorus leaching from macropores in undisturbed soil cores sampled across a natural clay gradient at Aarup, Denmark, were studied. The aim of the study...... was to correlate easily measurable soil properties, such as clay content and water-dispersible colloids, to colloid and phosphorus leaching. The clay contents across the gradient ranged from 0.11 to 0.23 kg kgj1. Irrigating with artificial rainwater, all samples showed a high first flush of colloids and phosphorus...

On the nature of fibres grown from nanodiamond colloids

Energy Technology Data Exchange (ETDEWEB)

Batsanov, Stepan S., E-mail: batsanov@mail.ru [National Research Institute of Physical-Technical Measurements, Moscow Region (Russian Federation); Guriev, Dmitry L.; Gavrilkin, Sergey M. [National Research Institute of Physical-Technical Measurements, Moscow Region (Russian Federation); Hamilton, Katherine A.; Lindsey, Keith [School of Biological and Biomedical Sciences, Durham University, Durham (United Kingdom); Mendis, Budhika G. [Physics Department, Durham University, Durham (United Kingdom); Riggs, Helen J.; Batsanov, Andrei S. [Chemistry Department, Durham University, Durham (United Kingdom)

2016-04-15

Contrary to earlier assumptions, the fibres spontaneously forming in aqueous colloids of detonation-produced nanodiamond (ND), do not consist purely of ND particles but are agglomerates of the latter with water and/or soft matter of biological (probably fungal) origin, as shown by elemental analysis, IR and Raman spectroscopy, X-ray diffraction, optical refractometry, optical and electron (TEM and ESEM)microscopy, as well as biological staining tests. - Graphical abstract: Fibres spontaneously formed in water colloids of nanodiamond, consist of diamond nanoparticles dispersed in bioorganic matter. - Highlights: • Entangled fibres slowly grow in dilute (∼0.1%) colloids of nanodiamond in water. • Refractive index (∼1.56), electron microscopy and CHN analysis indicate nanodiamond dispersed in organic matter. • Explanation: nanodiamond grains help the growth of fungi which assemble them.

On the nature of fibres grown from nanodiamond colloids

International Nuclear Information System (INIS)

Batsanov, Stepan S.; Guriev, Dmitry L.; Gavrilkin, Sergey M.; Hamilton, Katherine A.; Lindsey, Keith; Mendis, Budhika G.; Riggs, Helen J.; Batsanov, Andrei S.

2016-01-01

Contrary to earlier assumptions, the fibres spontaneously forming in aqueous colloids of detonation-produced nanodiamond (ND), do not consist purely of ND particles but are agglomerates of the latter with water and/or soft matter of biological (probably fungal) origin, as shown by elemental analysis, IR and Raman spectroscopy, X-ray diffraction, optical refractometry, optical and electron (TEM and ESEM)microscopy, as well as biological staining tests. - Graphical abstract: Fibres spontaneously formed in water colloids of nanodiamond, consist of diamond nanoparticles dispersed in bioorganic matter. - Highlights: • Entangled fibres slowly grow in dilute (∼0.1%) colloids of nanodiamond in water. • Refractive index (∼1.56), electron microscopy and CHN analysis indicate nanodiamond dispersed in organic matter. • Explanation: nanodiamond grains help the growth of fungi which assemble them.

Anomalous interactions in confined charge-stabilized colloid

International Nuclear Information System (INIS)

Grier, D G; Han, Y

2004-01-01

Charge-stabilized colloidal spheres dispersed in weak 1:1 electrolytes are supposed to repel each other. Consequently, experimental evidence for anomalous long-ranged like-charged attractions induced by geometric confinement inspired a burst of activity. This has largely subsided because of nagging doubts regarding the experiments' reliability and interpretation. We describe a new class of thermodynamically self-consistent colloidal interaction measurements that confirm the appearance of pairwise attractions among colloidal spheres confined by one or two bounding walls. In addition to supporting previous claims for this as-yet unexplained effect, these measurements also cast new light on its mechanism

Liquid crystal boojum-colloids

International Nuclear Information System (INIS)

Tasinkevych, M; Silvestre, N M; Telo da Gama, M M

2012-01-01

Colloidal particles dispersed in a liquid crystal (LC) lead to distortions of the director field. The distortions are responsible for long-range effective colloidal interactions whose asymptotic behaviour is well understood. The short-distance behaviour depends on the structure and dynamics of the topological defects nucleated near the colloidal particles and a full nonlinear theory is required to describe it. Spherical colloidal particles with strong planar degenerate anchoring nucleate a pair of antipodal surface topological defects, known as boojums. We use the Landau-de Gennes theory to resolve the mesoscopic structure of the boojum cores and to determine the pairwise colloidal interactions. We compare the results in three (3D) and two (2D) spatial dimensions for spherical and disc-like colloidal particles, respectively. The corresponding free energy functionals are minimized numerically using finite elements with adaptive meshes. Boojums are always point-like in 2D, but acquire a rather complex structure in 3D, which depends on the combination of the anchoring potential, the radius of the colloid, the temperature and the LC elastic anisotropy. We identify three types of defect cores in 3D that we call single, double and split-core boojums, and investigate the associated structural transitions. The split-core structure is favoured by low temperatures, strong anchoring and small twist to splay or bend ratios. For sufficiently strong anchoring potentials characterized by a well-defined uniaxial minimum, the split-core boojums are the only stable configuration. In the presence of two colloidal particles, we observe substantial re-arrangements of the inner defects in both 3D and 2D. These re-arrangements lead to qualitative changes in the force-distance profile when compared to the asymptotic quadrupole-quadrupole interaction. In line with the experimental results, the presence of the defects prevents coalescence of the colloidal particles in 2D, but not in 3D

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.

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

Energy Technology Data Exchange (ETDEWEB)

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

2012-08-01

movement were stronger than during the receding movement. Theory indicates that, for hydrophilic colloids, the advancing interface movement generally exerts a stronger detachment force than the receding, except when the hysteresis of the colloid-air-water contact angle is small. These results of our study are particularly relevant for colloid mobilization and transport related to three process in the vadose zone at Hanford: (1) water infiltration into sediments during rainfall or snowmelt events, (2) groundwater fluctuations as caused by river stage fluctuations, and (3) steady-state, low-flow recharge in deep vadose zone sediments. Transient water flow, like during infiltration or groundwater level fluctuations, are most conducive for colloid mobilization, but even during steady-state, low-flow recharge, colloids can be mobile, although to a much lesser extent. The results of this project have led to a comprehensive and fundamental understanding of colloid transport and mobilization under unsaturated flow conditions at the Hanford site.

Magnetoresponsive conductive colloidal suspensions with magnetized carbon nanotubes

Energy Technology Data Exchange (ETDEWEB)

Abdalla, Ahmed M. [Department of Engineering Physics, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4L7 (Canada); Abdel Fattah, Abdel Rahman [Department of Mechanical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4L7 (Canada); Ghosh, Suvojit [Department of Engineering Physics, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4L7 (Canada); Puri, Ishwar K., E-mail: ikpuri@mcmaster.ca [Department of Engineering Physics, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4L7 (Canada); Department of Mechanical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4L7 (Canada)

2017-01-01

We synthesize a novel and hitherto unreported class of colloidal suspensions for which the dispersed phase, which consists of multiwall carbon nanotubes (MWNTs) decorated with magnetic nanoparticles (MNPs), is both magnetoresponsive and electrically conductive. Synthesis of the dispersed phase merges processes for producing ferrofluids and magnetic MWNTs (mMWNTs). We explore means to tune the properties of these magnetic conductive colloids (MCCs) by varying the (1) MNP material composition, and (2) MNP:MWNT (w/w) magnetization weight ratio (γ). The mMWNTs are examined using XRD, TEM, EDX and SQUID and MCCs are by measuring their zeta potential and electric conductivity. Magnetite (Fe{sub 3}O{sub 4}) MNPs, which possess a high Curie temperature, produce mMWNTs with high saturation magnetization that respond relatively weakly to temperature variations. Mn{sub 0.2}Cu{sub 0.2}Zn{sub 0.6}Fe{sub 2}O{sub 4} and Cu{sub 0.4}Zn{sub 0.6}Fe{sub 2}O{sub 4} MNPs with lower Curie temperatures are more sensitive to changing temperature. Increasing the MNP Cu content improves the electric conductivity of the corresponding MCC while increasing γ enhances its magnetic response. After γ is raised above a threshold value, mMWNT decoration on the CNT surface becomes nonuniform since the MNPs now agglomerate perpendicular to the nanotube surface. These colloidal suspensions are a promising new class of material that can be manipulated with a magnetic field to tune their electrical conductivity. - Highlights: ●We synthesize a novel and hitherto unreported class of colloidal suspensions. ●These colloidal suspensions are both magnetoresponsive and electrically conductive. ●The dispersed phase consists of MWNTs decorated with different magnetic nanoparticles. ●These colloids have enhanced magnetic response and electric conductivity (up to 169.5 mS cm{sup −1}). ●It is a promising new class of material that can be manipulated with a magnetic field.

Sustainable steric stabilization of colloidal titania nanoparticles

Science.gov (United States)

Elbasuney, Sherif

2017-07-01

A route to produce a stable colloidal suspension is essential if mono-dispersed particles are to be successfully synthesized, isolated, and used in subsequent nanocomposite manufacture. Dispersing nanoparticles in fluids was found to be an important approach for avoiding poor dispersion characteristics. However, there is still a great tendency for colloidal nanoparticles to flocculate over time. Steric stabilization can prevent coagulation by introducing a thick adsorbed organic layer which constitutes a significant steric barrier that can prevent the particle surfaces from coming into direct contact. One of the main features of hydrothermal synthesis technique is that it offers novel approaches for sustainable nanoparticle surface modification. This manuscript reports on the sustainable steric stabilization of titanium dioxide nanoparticles. Nanoparticle surface modification was performed via two main approaches including post-synthesis and in situ surface modification. The tuneable hydrothermal conditions (i.e. temperature, pressure, flow rates, and surfactant addition) were optimized to enable controlled steric stabilization in a continuous fashion. Effective post synthesis surface modification with organic ligand (dodecenyl succinic anhydride (DDSA)) was achieved; the optimum surface coating temperature was reported to be 180-240 °C to ensure DDSA ring opening and binding to titania nanoparticles. Organic-modified titania demonstrated complete change in surface properties from hydrophilic to hydrophobic and exhibited phase transfer from the aqueous phase to the organic phase. Exclusive surface modification in the reactor was found to be an effective approach; it demonstrated surfactant loading level 2.2 times that of post synthesis surface modification. Titania was also stabilized in aqueous media using poly acrylic acid (PAA) as polar polymeric dispersant. PAA-titania nanoparticles demonstrated a durable amorphous polymeric layer of 2 nm thickness. This

Self-Supporting Nanodiamond Gels: Elucidating Colloidal Interactions Through Rheology_

Science.gov (United States)

Adhikari, Prajesh; Tripathi, Anurodh; Vogel, Nancy A.; Rojas, Orlando J.; Raghavan, Sriunivasa R.; Khan, Saad A.

This work investigates the colloidal interactions and rheological behavior of nanodiamond (ND) dispersions. While ND represents a promising class of nanofiller due to its high surface area, superior mechanical strength, tailorable surface functionality and biocompatibility, much remains unknown about the behavior of ND dispersions. We hypothesize that controlling interactions in ND dispersions will lead to highly functional systems with tunable modulus and shear response. Steady and dynamic rheology techniques are thus employed to systematically investigate nanodiamonds dispersed in model polar and non-polar media. We find that low concentrations of ND form gels almost instantaneously in a non-polar media. In contrast, ND's in polar media show a time-dependent behavior with the modulus increasing with time. We attribute the difference in behavior to variations in inter-particle interactions as well as the interaction of the ND with the media. Large steady and oscillatory strains are applied to ND colloidal gels to investigate the role of shear in gel microstructure breakdown and recovery. For colloidal gels in non-polar medium, the incomplete recovery of elastic modulus at high strain amplitudes indicates dominance of particle-particle interactions; however, in polar media the complete recovery of elastic modulus even at high strain amplitudes indicates dominance of particle-solvent interactions. These results taken together provide a platform to develop self-supporting gels with tunable properties in terms of ND concentration, and solvent type.

Colloid electrochemistry of conducting polymer: towards potential-induced in-situ drug release

International Nuclear Information System (INIS)

Sankoh, Supannee; Vagin, Mikhail Yu.; Sekretaryova, Alina N.; Thavarungkul, Panote; Kanatharana, Proespichaya; Mak, Wing Cheung

2017-01-01

Highlights: • Pulsed electrode potential induced an in-situ drug release from dispersion of conducting polymer microcapsules. • Fast detection of the released drug within the colloid microenvironment. • Improved the efficiency of localized drug release at the electrode interface. - Abstract: Over the past decades, controlled drug delivery system remains as one of the most important area in medicine for various diseases. We have developed a new electrochemically controlled drug release system by combining colloid electrochemistry and electro-responsive microcapsules. The pulsed electrode potential modulation led to the appearance of two processes available for the time-resolved registration in colloid microenvironment: change of the electronic charge of microparticles (from 0.5 ms to 0.1 s) followed by the drug release associated with ionic equilibration (1–10 s). The dynamic electrochemical measurements allow the distinction of drug release associated with ionic relaxation and the change of electronic charge of conducting polymer colloid microparticles. The amount of released drug (methylene blue) could be controlled by modulating the applied potential. Our study demonstrated a surface-potential driven controlled drug release of dispersion of conducting polymer carrier at the electrode interfaces, while the bulk colloids dispersion away from the electrode remains as a reservoir to improve the efficiency of localized drug release. The developed new methodology creates a model platform for the investigations of surface potential-induced in-situ electrochemical drug release mechanism.

Linear Optical Properties of Gold Colloid

Directory of Open Access Journals (Sweden)

Jingmin XIA

2015-11-01

Full Text Available Gold colloid was prepared by reducing HAuCl4·4H2O with Na3C6H5O7·2H2O. The morphology, size of gold nanoparticles and the optical property of colloid were characterized by transmission electron microscope and UV-Vis spectrophotometer, respectively. It shows that the gold nanoparticles are in the shape of spheres with diameters less than 8 nm, and the surface plasmon resonance absorption peak is located at about 438 nm. As the volume fraction of gold particles increases, the intensity of absorption peak strengthens. The optical property of gold colloid was analyzed by Maxwell-Garnett (MG effective medium theory in the company of Drude dispersion model. The results show that the matrix dielectric constant is a main factor, which influences the optical property of gold colloid.DOI: http://dx.doi.org/10.5755/j01.ms.21.4.9558

Deposition of bi-dispersed particles in inkjet-printed evaporating colloidal drops

Science.gov (United States)

Sun, Ying; Joshi, Abhijit; Chhasatia, Viral

2010-11-01

In this study, the deposition behaviors of inkjet-printed evaporating colloidal drops consisting of bi-dispersed micro and nano-sized particles are investigated by fluorescence microscopy and SEM. The results on hydrophilic glass substrates show that, evaporatively-driven outward flow drives the nanoparticles to deposit close to the pinned contact line while an inner ring deposition is formed by microparticles. This size-induced particle separation is consistent with the existence of a wedge-shaped drop edge near the contact line region of an evaporating drop on a hydrophilic substrate. The replenishing evaporatively-driven flow assembles nanoparticles closer to the pinned contact line forming an outer ring of nanoparticles and this particle jamming further enhances the contact line pinning. Microparticles are observed to form an inner ring inside the nano-sized deposits. This size-induced particle separation presents a new challenge to the uniformity of functional materials in bioprinting applications where nanoparticles and micro-sized cells are mixed together. On the other hand, particle self-assembly based on their sizes provides enables easy and well-controlled pattern formation. The effects of particle size contrast, particle volume fraction, substrate surface energy, and relative humidity of the printing environment on particle separation are examined in detail.

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.

Long-term Effects of Organic Waste Fertilizers on Soil Structure, Tracer Transport, and Leaching of Colloids.

Science.gov (United States)

Lekfeldt, Jonas Duus Stevens; Kjaergaard, Charlotte; Magid, Jakob

2017-07-01

Organic waste fertilizers have previously been observed to significantly affect soil organic carbon (SOC) content and soil structure. However, the effect of organic waste fertilizers on colloid dispersibility and leaching of colloids from topsoil has not yet been studied extensively. We investigated how the repeated application of different types of agricultural (liquid cattle slurry and solid cattle manure) and urban waste fertilizers (sewage sludge and composted organic household waste) affected soil physical properties, colloid dispersion from aggregates, tracer transport, and colloid leaching from intact soil cores. Total porosity was positively correlated with SOC content. Yearly applications of sewage sludge increased absolute microporosity (pores 30 μm) compared with the unfertilized control, whereas organic household waste compost fertilization increased both total porosity and the absolute porosity in all pore size classes (though not significant for 100-600 μm). Treatments receiving large amounts of organic fertilizers exhibited significantly lower levels of dispersible colloids compared with an unfertilized control and a treatment that had received moderate applications of cattle slurry. The content of water-dispersible colloids could not be explained by a single factor, but differences in SOC content, electrical conductivity, and sodium adsorption ratio were important factors. Moreover, we found that the fertilizer treatments did not significantly affect the solute transport properties of the topsoil. Finally, we found that the leaching of soil colloids was significantly decreased in treatments that had received large amounts of organic waste fertilizers, and we ascribe this primarily to treatment-induced differences in effluent electrical conductivity during leaching. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Lysine-functionalized nanodiamonds as gene carriers: development of stable colloidal dispersion for in vitro cellular uptake studies and siRNA delivery application

Directory of Open Access Journals (Sweden)

Alwani S

2016-02-01

Full Text Available Saniya Alwani,1 Randeep Kaur,1 Deborah Michel,1 Jackson M Chitanda,2 Ronald E Verrall,3 Chithra Karunakaran,4 Ildiko Badea1 1Drug Design and Discovery Research Group, College of Pharmacy and Nutrition, 2Department of Chemical & Biological Engineering, 3Department of Chemistry, University of Saskatchewan, 4Canadian Light Source, Saskatoon, SK, Canada Purpose: Nanodiamonds (NDs are emerging as an attractive tool for gene therapeutics. To reach their full potential for biological application, NDs should maintain their colloidal stability in biological milieu. This study describes the behavior of lysine-functionalized ND (lys-ND in various dispersion media, with an aim to limit aggregation and improve the colloidal stability of ND-gene complexes called diamoplexes. Furthermore, cellular and macromolecular interactions of lys-NDs are also analyzed in vitro to establish the understanding of ND-mediated gene transfer in cells. Methods: lys-NDs were synthesized earlier through covalent conjugation of lysine amino acid to carboxylated NDs surface generated through re-oxidation in strong oxidizing acids. In this study, dispersions of lys-NDs were prepared in various media, and the degree of sedimentation was monitored for 72 hours. Particle size distributions and zeta potential measurements were performed for a period of 25 days to characterize the physicochemical stability of lys-NDs in the medium. The interaction profile of lys-NDs with fetal bovine serum showed formation of a protein corona, which was evaluated by size and charge distribution measurements. Uptake of lys-NDs in cervical cancer cells was analyzed by scanning transmission X-ray microscopy, flow cytometry, and confocal microscopy. Cellular uptake of diamoplexes (complex of lys-NDs with small interfering RNA was also analyzed using flow cytometry. Results: Aqueous dispersion of lys-NDs showed minimum sedimentation and remained stable over a period of 25 days. Size distributions showed

Viscothermal Coupling Effects on Sound Attenuation in Concentrated Colloidal Dispersions.

Science.gov (United States)

Han, Wei

1995-11-01

spheroids, is developed and applied to estimate the viscous attenuation coefficients. With incorporation of particle size and shape distributions (PSSD), predictions agree quantitatively with observed attenuation coefficients. The effects of particle aspect ratio and orientation become more evident as particle concentrations and frequencies are increased. The UCPC model combined with the ultrasonic spectroscopy techniques can provide for theoretical and experimental frameworks in characterization of concentrated colloidal dispersions.

Antimicrobial Peptide-Driven Colloidal Transformations in Liquid-Crystalline Nanocarriers

DEFF Research Database (Denmark)

Gontsarik, Mark; Buhmann, Matthias T; Yaghmur, Anan

2016-01-01

Designing efficient colloidal systems for the delivery of membrane active antimicrobial peptides requires in-depth understanding of their structural and morphological characteristics. Using dispersions of inverted type bicontinuous cubic phase (cubosomes), we examine the effect of integrating...... structure, inducing colloidal transformations to sponge and lamellar phases and micelles in a concentration-dependent manner. These investigations, together with in vitro evaluation studies using a clinically relevant bacterial strain, established the composition-nanostructure-activity relationship that can...

Slow Auger Relaxation in HgTe Colloidal Quantum Dots.

Science.gov (United States)

Melnychuk, Christopher; Guyot-Sionnest, Philippe

2018-05-03

The biexciton lifetimes in HgTe colloidal quantum dots are measured as a function of particle size. Samples produced by two synthetic methods, leading to partially aggregated or well-dispersed particles, exhibit markedly different dynamics. The relaxation characteristics of partially aggregated HgTe inhibit reliable determinations of the Auger lifetime. In well-dispersed HgTe quantum dots, the biexciton lifetime increases approximately linearly with particle volume, confirming trends observed in other systems. The extracted Auger coefficient is three orders of magnitude smaller than that for bulk HgCdTe materials with similar energy gaps. We discuss these findings in the context of understanding Auger relaxation in quantum-confined systems and their relevance to mid-infrared optoelectronic devices based on HgTe colloidal quantum dots.

Valence holes observed in nanodiamonds dispersed in water

Science.gov (United States)

Petit, Tristan; Pflüger, Mika; Tolksdorf, Daniel; Xiao, Jie; Aziz, Emad F.

2015-02-01

Colloidal dispersion is essential for most nanodiamond applications, but its influence on nanodiamond electronic properties remains unknown. Here we have probed the electronic structure of oxidized detonation nanodiamonds dispersed in water by using soft X-ray absorption and emission spectroscopies at the carbon and oxygen K edges. Upon dispersion in water, the π* transitions from sp2-hybridized carbon disappear, and holes in the valence band are observed.Colloidal dispersion is essential for most nanodiamond applications, but its influence on nanodiamond electronic properties remains unknown. Here we have probed the electronic structure of oxidized detonation nanodiamonds dispersed in water by using soft X-ray absorption and emission spectroscopies at the carbon and oxygen K edges. Upon dispersion in water, the π* transitions from sp2-hybridized carbon disappear, and holes in the valence band are observed. Electronic supplementary information (ESI) available: Experimental methods, details on XAS/XES normalization and background correction procedures. See DOI: 10.1039/c4nr06639a

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.

Colloid suspension stability and transport through unsaturated porous media

International Nuclear Information System (INIS)

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

1997-04-01

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

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.)

Tuning the morphology, stability and photocatalytic activity of TiO2 nanocrystal colloids by tungsten doping

International Nuclear Information System (INIS)

Xu, Haiping; Liao, Jianhua; Yuan, Shuai; Zhao, Yin; Zhang, Meihong; Wang, Zhuyi; Shi, Liyi

2014-01-01

Graphical abstract: - Highlights: • W 6+ -doped TiO 2 nanocrystal colloids were prepared by hydrothermal methods. • The properties of TiO 2 nanocrystal colloids can be tuned by tungsten doping. • W 6+ -doped TiO 2 nanocrystal colloids show higher stability and dispersity. • W 6+ -doped TiO 2 nanocrystal colloids show higher photocatalytic activity. - Abstract: The effects of tungsten doping on the morphology, stability and photocatalytic activity of TiO 2 nanocrystal colloids were investigated. The nanostructure, chemical state of Ti, W, O, and the properties of tungsten doped TiO 2 samples were investigated carefully by TEM, XRD, XPS, UV–vis, PL and photocatalytic degradation experiments. And the structure–activity relationship was discussed according to the analysis and measurement results. The analysis results reveal that the morphology, zeta potential and photocatalytic activity of TiO 2 nanocrystals can be easily tuned by changing the tungsten doping concentration. The tungsten doped TiO 2 colloid combines the characters of high dispersity and high photocatalytic activity

Colloid and interface chemistry for nanotechnology

CERN Document Server

Kralchevsky, Peter; Ravera, Francesca

2016-01-01

Colloid and interface science dealt with nanoscale objects for nearly a century before the term nanotechnology was coined. An interdisciplinary field, it bridges the macroscopic world and the small world of atoms and molecules. Colloid and Interface Chemistry for Nanotechnology is a collection of manuscripts reflecting the activities of research teams that have been involved in the networking project Colloid and Interface Chemistry for Nanotechnology (2006-2011), Action D43, the European Science Foundation. The project was a part of the intergovernmental framework for Cooperation in Science and Technology (COST), allowing the coordination of nationally funded research across Europe. With contributions by leading experts, this book covers a wide range of topics. Chapters are grouped into three sections: "Nanoparticle Synthesis and Characterization," "New Experimental Tools and Interpretation," and "Nanocolloidal Dispersions and Interfaces." The topics covered belong to six basic research areas: (1) The synthes...

Wetting Behavior in Colloid-Polymer Mixtures at Different Substrates.

Science.gov (United States)

Wijting, Willem K; Besseling, Nicolaas A M; Cohen Stuart, Martien A

2003-09-25

We present experimental observations on wetting phenomena in depletion interaction driven, phase separated colloidal dispersions. The contact angle of the colloidal liquid-gas interface at a solid substrate was determined for a series of compositions. Upon approach to the critical point, a transition occurs from partial to complete wetting. The interaction with the substrate was manipulated by modifying the substrate with a polymer. In that case, a transition from partial to complete drying is observed upon approach to the critical point.

Long-term aging behaviors in a model soft colloidal system.

Science.gov (United States)

Li, Qi; Peng, Xiaoguang; McKenna, Gregory B

2017-02-15

Colloidal and molecular systems share similar behaviors near to the glass transition volume fraction or temperature. Here, aging behaviors after volume fraction up-jump (induced by performing temperature down-jumps) conditions for a PS-PNIPAM/AA soft colloidal system were investigated using light scattering (diffusing wave spectroscopy, DWS). Both aging responses and equilibrium dynamics were investigated. For the aging responses, long-term experiments (100 000 s) were performed, and both equilibrium and non-equilibrium behaviors of the system were obtained. In the equilibrium state, as effective volume fraction increases (or temperature decreases), the colloidal dispersion displays a transition from the liquid to a glassy state. The equilibrium α-relaxation dynamics strongly depend on both the effective volume fraction and the initial mass concentration for the studied colloidal systems. Compared with prior results from our lab [X. Di, X. Peng and G. B. McKenna, J. Chem. Phys., 2014, 140, 054903], the effective volume fractions investigated spanned a wider range, to deeper into the glassy domain. The results show that the α-relaxation time τ α of the samples aged into equilibrium deviate from the classical Vogel-Fulcher-Tammann (VFT)-type expectations and the super-Arrhenius signature disappears above the glass transition volume fraction. The non-equilibrium aging response shows that the time for the structural evolution into equilibrium and the α-relaxation time are decoupled. The DWS investigation of the aging behavior after different volume fraction jumps reveals a different non-equilibrium or aging behavior for the considered colloidal systems compared with either molecular glasses or the macroscopic rheology of a similar colloidal dispersions.

Uranium facilitated transport by water-dispersible colloids in field and soil columns

Energy Technology Data Exchange (ETDEWEB)

Crancon, P., E-mail: pierre.crancon@cea.fr [CEA, DAM, DIF, F-91297 Arpajon (France); Pili, E. [CEA, DAM, DIF, F-91297 Arpajon (France); Charlet, L. [Laboratoire de Geophysique Interne et Tectonophysique (LGIT-OSUG), University of Grenoble-I, UMR5559-CNRS-UJF, BP53, 38041 Grenoble cedex 9 (France)

2010-04-01

The transport of uranium through a sandy podzolic soil has been investigated in the field and in column experiments. Field monitoring, numerous years after surface contamination by depleted uranium deposits, revealed a 20 cm deep uranium migration in soil. Uranium retention in soil is controlled by the < 50 {mu}m mixed humic and clayey coatings in the first 40 cm i.e. in the E horizon. Column experiments of uranium transport under various conditions were run using isotopic spiking. After 100 pore volumes elution, 60% of the total input uranium is retained in the first 2 cm of the column. Retardation factor of uranium on E horizon material ranges from 1300 (column) to 3000 (batch). In parallel to this slow uranium migration, we experimentally observed a fast elution related to humic colloids of about 1-5% of the total-uranium input, transferred at the mean porewater velocity through the soil column. In order to understand the effect of rain events, ionic strength of the input solution was sharply changed. Humic colloids are retarded when ionic strength increases, while a major mobilization of humic colloids and colloid-borne uranium occurs as ionic strength decreases. Isotopic spiking shows that both {sup 238}U initially present in the soil column and {sup 233}U brought by input solution are desorbed. The mobilization process observed experimentally after a drop of ionic strength may account for a rapid uranium migration in the field after a rainfall event, and for the significant uranium concentrations found in deep soil horizons and in groundwater, 1 km downstream from the pollution source.

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.

Dispersion and absorption of longitudinal electro-kinetic wave in ion-implanted GaN semiconductor plasmas

Energy Technology Data Exchange (ETDEWEB)

Soni, Dilip [Government P G Madhav Science College, Ujjain (M P) (India); Sharma, Giriraj, E-mail: grsharma@gmail.com [SRJ Government Girls’ College, Neemuch (M P) (India); Saxena, Ajay [Government College, Garoth, Dist. Mandsaur (M P) (India); Jadhav, Akhilesh [Government J Yoganandam Chhattisgarh College, Raipur (C G) (India)

2015-07-31

An analytical study on propagation characteristics of longitudinal electro-kinetic (LEK) waves is presented. Based on multi-fluid model of plasma, we have derived a dispersion relation for LEK waves in colloid laden GaN semiconductor plasmas. It is assumed that ions are implanted to form colloids in the GaN sample. The colloids are continuously bombarded by the plasma particles and stick on them, but they acquire a net negative charge due to relatively higher mobility of electrons. It is found from the dispersion relation that the presence of charged colloids not only modifies the existing modes but also supports new novel modes of LEKWs. It is hoped that the study would enhance understanding on dispersion and absorption of LEKWs and help in singling out the appropriate configurations in which GaN crystal would be better suited for fabrication of microwave devices.

Uranium facilitated transport by water-dispersible colloids in field and soil columns

Energy Technology Data Exchange (ETDEWEB)

Crancon, P.; Pili, E. [CEA Bruyeres-le-Chatel, DIF, 91 (France); Charlet, L. [Univ Grenoble 1, Lab Geophys Interne and Tectonophys LGIT OSUG, CNRS, UJF, UMR5559, F-38041 Grenoble 9 (France)

2010-07-01

The transport of uranium through a sandy podsolic soil has been investigated in the field and in column experiments. Field monitoring, numerous years after surface contamination by depleted uranium deposits, revealed a 20 cm deep uranium migration in soil. Uranium retention in soil is controlled by the {<=} 50 {mu}m mixed humic and clayey coatings in the first 40 cm i.e. in the E horizon. Column experiments of uranium transport under various conditions were run using isotopic spiking. After 100 pore volumes elution, 60% of the total input uranium is retained in the first 2 cm of the column. Retardation factor of uranium on E horizon material ranges from 1300 (column) to 3000 (batch). In parallel to this slow uranium migration, we experimentally observed a fast elution related to humic colloids of about 1-5% of the total-uranium input, transferred at the mean pore-water velocity through the soil column. In order to understand the effect of rain events, ionic strength of the input solution was sharply changed. Humic colloids are retarded when ionic strength increases, while a major mobilization of humic colloids and colloid-borne uranium occurs as ionic strength decreases. Isotopic spiking shows that both {sup 238}U initially present in the soil column and {sup 233}U brought by input solution are desorbed. The mobilization process observed experimentally after a drop of ionic strength may account for a rapid uranium migration in the field after a rainfall event, and for the significant uranium concentrations found in deep soil horizons and in groundwater, 1 km downstream from the pollution source. (authors)

Lysine-functionalized nanodiamonds as gene carriers: development of stable colloidal dispersion for in vitro cellular uptake studies and siRNA delivery application

Science.gov (United States)

Alwani, Saniya; Kaur, Randeep; Michel, Deborah; Chitanda, Jackson M; Verrall, Ronald E; Karunakaran, Chithra; Badea, Ildiko

2016-01-01

Purpose Nanodiamonds (NDs) are emerging as an attractive tool for gene therapeutics. To reach their full potential for biological application, NDs should maintain their colloidal stability in biological milieu. This study describes the behavior of lysine-functionalized ND (lys-ND) in various dispersion media, with an aim to limit aggregation and improve the colloidal stability of ND-gene complexes called diamoplexes. Furthermore, cellular and macromolecular interactions of lys-NDs are also analyzed in vitro to establish the understanding of ND-mediated gene transfer in cells. Methods lys-NDs were synthesized earlier through covalent conjugation of lysine amino acid to carboxylated NDs surface generated through re-oxidation in strong oxidizing acids. In this study, dispersions of lys-NDs were prepared in various media, and the degree of sedimentation was monitored for 72 hours. Particle size distributions and zeta potential measurements were performed for a period of 25 days to characterize the physicochemical stability of lys-NDs in the medium. The interaction profile of lys-NDs with fetal bovine serum showed formation of a protein corona, which was evaluated by size and charge distribution measurements. Uptake of lys-NDs in cervical cancer cells was analyzed by scanning transmission X-ray microscopy, flow cytometry, and confocal microscopy. Cellular uptake of diamoplexes (complex of lys-NDs with small interfering RNA) was also analyzed using flow cytometry. Results Aqueous dispersion of lys-NDs showed minimum sedimentation and remained stable over a period of 25 days. Size distributions showed good stability, remaining under 100 nm throughout the testing period. A positive zeta potential of >+20 mV indicated a preservation of surface charges. Size distribution and zeta potential changed for lys-NDs after incubation with blood serum, suggesting an interaction with biomolecules, mainly proteins, and a possible formation of a protein corona. Cellular internalization

Lysine-functionalized nanodiamonds as gene carriers: development of stable colloidal dispersion for in vitro cellular uptake studies and siRNA delivery application.

Science.gov (United States)

Alwani, Saniya; Kaur, Randeep; Michel, Deborah; Chitanda, Jackson M; Verrall, Ronald E; Karunakaran, Chithra; Badea, Ildiko

2016-01-01

Nanodiamonds (NDs) are emerging as an attractive tool for gene therapeutics. To reach their full potential for biological application, NDs should maintain their colloidal stability in biological milieu. This study describes the behavior of lysine-functionalized ND (lys-ND) in various dispersion media, with an aim to limit aggregation and improve the colloidal stability of ND-gene complexes called diamoplexes. Furthermore, cellular and macromolecular interactions of lys-NDs are also analyzed in vitro to establish the understanding of ND-mediated gene transfer in cells. lys-NDs were synthesized earlier through covalent conjugation of lysine amino acid to carboxylated NDs surface generated through re-oxidation in strong oxidizing acids. In this study, dispersions of lys-NDs were prepared in various media, and the degree of sedimentation was monitored for 72 hours. Particle size distributions and zeta potential measurements were performed for a period of 25 days to characterize the physicochemical stability of lys-NDs in the medium. The interaction profile of lys-NDs with fetal bovine serum showed formation of a protein corona, which was evaluated by size and charge distribution measurements. Uptake of lys-NDs in cervical cancer cells was analyzed by scanning transmission X-ray microscopy, flow cytometry, and confocal microscopy. Cellular uptake of diamoplexes (complex of lys-NDs with small interfering RNA) was also analyzed using flow cytometry. Aqueous dispersion of lys-NDs showed minimum sedimentation and remained stable over a period of 25 days. Size distributions showed good stability, remaining under 100 nm throughout the testing period. A positive zeta potential of >+20 mV indicated a preservation of surface charges. Size distribution and zeta potential changed for lys-NDs after incubation with blood serum, suggesting an interaction with biomolecules, mainly proteins, and a possible formation of a protein corona. Cellular internalization of lys-NDs was confirmed

Sustainable steric stabilization of colloidal titania nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Elbasuney, Sherif, E-mail: sherif_basuney2000@yahoo.com

2017-07-01

Graphical abstract: Controlled surface properties of titania nanoparticles via surface modification, flocculation from aqueous phase (a), stabilization in aqueous phase (b), extraction to organic phase (c). - Highlights: • Complete change in surface properties of titania nanoparticles from hydrophilic to hydrophobic. • Harvesting the formulated nanoparticles from the aqueous phase to the organic phase. • Exclusive surface modification in the reactor during nanoparticle synthesis. • Sustainable stabilization of titania nanoparticles in aqueous media with polar polymeric dispersant. - Abstract: A route to produce a stable colloidal suspension is essential if mono-dispersed particles are to be successfully synthesized, isolated, and used in subsequent nanocomposite manufacture. Dispersing nanoparticles in fluids was found to be an important approach for avoiding poor dispersion characteristics. However, there is still a great tendency for colloidal nanoparticles to flocculate over time. Steric stabilization can prevent coagulation by introducing a thick adsorbed organic layer which constitutes a significant steric barrier that can prevent the particle surfaces from coming into direct contact. One of the main features of hydrothermal synthesis technique is that it offers novel approaches for sustainable nanoparticle surface modification. This manuscript reports on the sustainable steric stabilization of titanium dioxide nanoparticles. Nanoparticle surface modification was performed via two main approaches including post-synthesis and in situ surface modification. The tuneable hydrothermal conditions (i.e. temperature, pressure, flow rates, and surfactant addition) were optimized to enable controlled steric stabilization in a continuous fashion. Effective post synthesis surface modification with organic ligand (dodecenyl succinic anhydride (DDSA)) was achieved; the optimum surface coating temperature was reported to be 180–240 °C to ensure DDSA ring opening

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

NARCIS (Netherlands)

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

2013-01-01

In 1861 Thomas Graham gave birth to a new field of science, today known as colloid science. Nowadays, the notion “colloid” is often used referring to systems consisting of two immiscible phases, one of which is finely dispersed into the other. Research on colloids deals mostly with sols (solids

The effect of colloid preload versus prophylactic ephedrine ...

African Journals Online (AJOL)

Aim: We aimed to investigate the effect of colloid infusion immediately before the spinal anesthesia, and the prophylactic intravenous (IV) infusion of ephedrine after injection of intrathecal bupivacaine on hemodynamic parameters, QT, The QT interval corrected for heart rate (QTc), and dispersion of QTc (QTcDisp) intervals ...

Phase behaviour of rod-like colloid + flexible polymer mixtures

NARCIS (Netherlands)

Lekkerkerker, H.N.W.; Stroobants, A.

The effect of non-adsorbing, flexible polymer on the isotropic-nematic transition in dispersions of rod-like colloids is investigated. A widening of the biphasic gap is observed, in combination with a marked polymer partitioning between the coexisting phases. Under certain conditions, areas of

Influence of Corynebacterium parvum on the phagocytosis of 198Au colloids in rats

International Nuclear Information System (INIS)

Bergoc, R.M.; Bianchin, A.M.; Caro, R.A.; Ihlo, J.E.; Rivera, E.S.

1982-01-01

The kinetics of the phagocytosis of gelatin-protected 198 Au colloids in Wistar rats treated with Corynebacterium Parvum (CBP), was studied in order to explain its mechanism of immunomodulation. A previously developed extracorporeal blood circulation technique was used. The changes in the rate of phagocytosis, v, after the administration of CBP, for a dose of the 198 Au colloid smaller or higher than the substratum constant, were studied. In the first case, no significant changes of v were observed; in the second case, significant increases of v were determined, which reached a maximum 6 days after the CBP administration. The kinetic analysis of the obtained data indicates that the action of CBP is exerted on the stage of the entrance of the colloidal particle into the reticuloendothelial cell. (author) [es

Photochemical Synthesis and Properties of Colloidal Copper, Silver and Gold Adsorbed on Quartz

International Nuclear Information System (INIS)

Loginov, Anatoliy V.; Gorbunova, Valentina V.; Boitsova, Tatiana B.

2002-01-01

Original methods for the photochemical production of stable copper, silver and gold colloids in the form of films on quartz, and dispersion in liquids were devised. It is shown that photochemical synthesis of colloidal metals is a difficult multiphase process, and includes the formation of low-valence forms of Cu(I), Au(I) and nonmetal clusters, colloidal particles and their agglomerates. Cluster stabilization and further growth to colloidal particles are achieved by adsorption onto the solid surface (quartz) or by increasing the viscosity of photolyte. In the absence of these methods of stabilization, the processes of intermediate reoxidation to Cu(II) and Au(III) and agglomeration of Ag and Au colloids proceed in a photolyte. Adsorption and the rate of cluster growth on a quartz surface are speeded up by the action of monochromatic UV light. Experimental models of the mechanism of colloidal formation are suggested. The dependence of the growth rate and the properties of the colloids on conditions of the photochemical procedure (energy and light intensity, concentration of initial complex) has been established

Physical aging and structural recovery in a colloidal glass subjected to volume-fraction jump conditions

Science.gov (United States)

Peng, Xiaoguang; McKenna, Gregory B.

2016-04-01

Three important kinetic phenomena have been cataloged by Kovacs in the investigation of molecular glasses during structural recovery or physical aging. These are responses to temperature-jump histories referred to as intrinsic isotherms, asymmetry of approach, and memory effect. Here we use a thermosensitive polystyrene-poly (N -isopropylacrylamide)-poly (acrylic acid) core-shell particle-based dispersion as a colloidal model and by working at a constant number concentration of particles we use temperature changes to create volume-fraction changes. This imposes conditions similar to those defined by Kovacs on the colloidal system. We use creep experiments to probe the physical aging and structural recovery behavior of colloidal glasses in the Kovacs-type histories and compare the results with those seen in molecular glasses. We find that there are similarities in aging dynamics between molecular glasses and colloidal glasses, but differences also persist. For the intrinsic isotherms, the times teq needed for relaxing or evolving into the equilibrium (or stationary) state are relatively insensitive to the volume fraction and the values of teq are longer than the α -relaxation time τα at the same volume fraction. On the other hand, both of these times grow at least exponentially with decreasing temperature in molecular glasses. For the asymmetry of approach, similar nonlinear behavior is observed for both colloidal and molecular glasses. However, the equilibration time teq is the same for both volume-fraction up-jump and down-jump experiments, different from the finding in molecular glasses that it takes longer for the structure to evolve into equilibrium for the temperature up-jump condition than for the temperature down-jump condition. For the two-step volume-fraction jumps, a memory response is observed that is different from observations of structural recovery in two-step temperature histories in molecular glasses. The concentration dependence of the dynamics

Synthesis of nanosized silver colloids by microwave dielectric heating

Indian Academy of Sciences (India)

Silver nanosized crystallites have been synthesized in aqueous and polyols viz., ethylene glycol and glycerol, using a microwave technique. Dispersions of colloidal silver have been prepared by the reduction of silver nitrate both in the presence and absence of stabilizer poly(vinylpyrolidone) (PVP). It was observed that ...

A study on the characteristics of colloid-associated radionuclide transport in porous media

International Nuclear Information System (INIS)

Jeong, Yun Chang

1997-02-01

Recently, the radionuclide transport in the form of colloids has been focused intensively in the safety assessment of a radioactive waste repository. As colloids are considered to be able to increase the transport rate of radionuclide through geologic media, the transport of radionuclide should be adjusted by the presence of colloids. The migration of dissolved radionuclide is expected to depend on various process such as advection, dispersion and interactions with soils, and, in addition, the transport of colloid-mediated radionuclide is considered to be more complicated because of the interactions between radionuclides and colloids. In this paper the migration behavior of colloid-associated radionuclides within subsurface are reviewed and studied in detail. The colloid-mediated transport system was modelled and simulated in order to illustrate the effects of colloids on the transport of radionuclide in the aquifer system. The transport rate of radionuclide is mainly controlled by a retardation factor which is controlled by colloidal behaviors, degree of adsorption, and the related geologic parameters. Therefore it is necessary to carefully understand the accelerating tendency of the retardation difference factor, and in this study the trends are analyzed, described and the retardation difference factor is mathematically defined, simplified and applied practically to the safety and performance assessment of a future repository

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

Dispersion for the preparation of an injectable radiopharmaceutical scanning agent

International Nuclear Information System (INIS)

Wolfangel, R.G.

1976-01-01

The invention deals with the preparation of a dispersion of a tin (II) sulphur colloid in an aqueous solution with additions of a stabilizing agent. Labelled with sup(99m)Tc, the dispersion can be used as an injectable radiopharmaceutical scanning agent. (VJ) [de

Influence of Corynebacterium parvum on the phagocytosis of /sup 198/Au colloids in rats

Energy Technology Data Exchange (ETDEWEB)

Bergoc, R.M.; Bianchin, A.M.; Caro, R.A.; Ihlo, J.E.; Rivera, E.S. (Buenos Aires Univ. Nacional (Argentina). Facultad de Farmacia y Bioquimica)

1982-07-01

The kinetics of the phagocytosis of gelatin-protected /sup 198/Au colloids in Wistar rats treated with Corynebacterium Parvum (CBP), was studied in order to explain its mechanism of immunomodulation. A previously developed extracorporeal blood circulation technique was used. The changes in the rate of phagocytosis, v, after the administration of CBP, for a dose of the /sup 198/Au colloid smaller or higher than the substratum constant, were studied. In the first case, no significant changes of v were observed; in the second case, significant increases of v were determined, which reached a maximum 6 days after the CBP administration. The kinetic analysis of the obtained data indicates that the action of CBP is exerted on the stage of the entrance of the colloidal particle into the reticuloendothelial cell.

Controlled synthesis of colloidal silver nanoparticles in capillary micro-flow reactor

International Nuclear Information System (INIS)

He Shengtai; Liu Yulan; Maeda, Hideaki

2008-01-01

In this study, using a polytetrafluoroethylene (PTFE) capillary tube as a micro-flow reactor, well-dispersed colloidal silver nanoparticles were controllably synthesized with different flow rates of precursory solution. Scanning transmission electron microscopy images and UV-visible absorbance spectra showed that silver nanoparticles with large size can be prepared with slow flow rate in the PTFE capillary reactor. The effects of tube diameters on the growth of colloidal silver nanoparticles were investigated. Experiment results demonstrated that using tube with small diameter was more propitious for the controllable synthesis of silver nanoparticles with different sizes.

THE STUDYING OF COLLOIDAL-CHEMICAL PROPERTIES OF CLAY MINERALS DISPERSIONS

Directory of Open Access Journals (Sweden)

A. F. Tymchuk

2015-02-01

Full Text Available The element structure is studied, the microscopic analysis of fine-dispersed min­eral systems (ground sediments of a mouth of the river Danube is carried out. The sedimentation process of clay minerals dispersions in solutions of surfactants and macromolecular substances is studied. Concentration intervals of stabilization of investigating dispersions were defined.

Use of nuclear recoil for separating 228Ra, 224Ra, and 233Pa from colloidal thorium

International Nuclear Information System (INIS)

Beydon, J.; Gratot, I.

1968-01-01

By using α-recoil it is possible to separate by dialysis the α disintegration products (224 Ra; 228 Ra) of thorium from colloidal thorium hydroxide.The use of n, γ recoil allows the separation of 233 Pa produced by the neutron irradiation of thorium, on condition that the colloidal thorium hydroxide is irradiated in the presence of a dispersing. (author) [fr

Colloidal mobilization of arsenic from mining-affected soils by surface runoff.

Science.gov (United States)

Gomez-Gonzalez, Miguel Angel; Voegelin, Andreas; Garcia-Guinea, Javier; Bolea, Eduardo; Laborda, Francisco; Garrido, Fernando

2016-02-01

Scorodite-rich wastes left as a legacy of mining and smelting operations pose a threat to environmental health. Colloids formed by the weathering of processing wastes may control the release of arsenic (As) into surface waters. At a former mine site in Madrid (Spain), we investigated the mobilization of colloidal As by surface runoff from weathered processing wastes and from sediments in the bed of a draining creek and a downstream sedimentation-pond. Colloids mobilized by surface runoff during simulated rain events were characterized for their composition, structure and mode of As uptake using asymmetric flow field-flow fractionation coupled to inductively plasma mass spectrometry (AF4-ICP-MS) and X-ray absorption spectroscopy (XAS) at the As and Fe K-edges. Colloidal scorodite mobilized in surface runoff from the waste pile is acting as a mobile As carrier. In surface runoff from the river bed and the sedimentation pond, ferrihydrite was identified as the dominant As-bearing colloidal phase. The results from this study suggest that mobilization of As-bearing colloids by surface runoff may play an important role in the dispersion of As from metallurgical wastes deposited above ground and needs to be considered in risk assessment. Copyright © 2015 Elsevier Ltd. All rights reserved.

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

Surface self-assembly of fluorosurfactants during film formation of MMA/nBA colloidal dispersions.

Science.gov (United States)

Dreher, W R; Urban, M W

2004-11-23

These studies focus on the behavior of fluorosurfactants (FS) containing hydrophobic and ionic entities in the presence of methyl methacrylate/n-butyl acrylate (MMA/nBA) colloidal dispersions stabilized by sodium dodecyl sulfate (SDS). The presence of FS significantly not only alters the mobility of SDS in MMA/nBA films, but their hydrophobic and ionic nature results in self-assembly near the film-air (F-A) interface leading to different surface morphologies. Spherical islands and rodlike morphologies are formed which diminish the kinetic coefficient of friction of films by at least 3 orders of magnitude, and the presence of dual hydrophobic tails and an anionic head appears to have the largest effect on the surface friction. Using internal reflection IR imaging, these studies show that structural and chemical features of FS are directly related to their ability to migrate to the F-A interface and self-assemble to form specific morphological features. While the anionic nature of FS allows for SDS migration to the F-A interface and the formation of stable domains across the surface, intermolecular cohesion of nonionic FS allows for the formation of rodlike structures due to inability to form mixed micelles with SDS. These studies also establish the relationship between surface morphologies, kinetic coefficient of friction, and structural features of surfactants in the complex environments.

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)

Tailoring particle size and morphology of colloidal Ag particles via chemical precipitation for Ag-BSCCO composites

International Nuclear Information System (INIS)

Medendorp, N.W. Jr.; Bowman, K.J.; Trumble, K.P.

1996-01-01

The chemical precipitation of silver particles is an effective method for tailoring the particle size and morphology. This article investigates a chemical precipitation method for producing silver colloids, and how processing parameters affected particle size, morphology and adherence. Decreasing the silver nitrate concentration during precipitation with sodium borohydride decreased the colloidal silver particle size. Decreasing the addition rate of the reducing agent produced faceted particles. Reversing the reactant addition order also changed the particle size and the morphology. Precipitated colloids demonstrated a difference between the growth-dominated and the equilibrium structures. Co-dispersing Bi-based superconducting platelets during precipitation allowed Ag colloids to preferentially nucleate on the platelets and to remain adhered even after the additional processing. (orig.)

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.

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

Colloidal graphite/graphene nanostructures using collagen showing enhanced thermal conductivity

Science.gov (United States)

Bhattacharya, Soumya; Dhar, Purbarun; Das, Sarit K; Ganguly, Ranjan; Webster, Thomas J; Nayar, Suprabha

2014-01-01

In the present study, the exfoliation of natural graphite (GR) directly to colloidal GR/graphene (G) nanostructures using collagen (CL) was studied as a safe and scalable process, akin to numerous natural processes and hence can be termed “biomimetic”. Although the exfoliation and functionalization takes place in just 1 day, it takes about 7 days for the nano GR/G flakes to stabilize. The predominantly aromatic residues of the triple helical CL forms its own special micro and nanoarchitecture in acetic acid dispersions. This, with the help of hydrophobic and electrostatic forces, interacts with GR and breaks it down to nanostructures, forming a stable colloidal dispersion. Surface enhanced Raman spectroscopy, X-ray diffraction, photoluminescence, fluorescence, and X-ray photoelectron spectroscopy of the colloid show the interaction between GR and CL on day 1 and 7. Differential interference contrast images in the liquid state clearly reveal how the GR flakes are entrapped in the CL fibrils, with a corresponding fluorescence image showing the intercalation of CL within GR. Atomic force microscopy of graphene-collagen coated on glass substrates shows an average flake size of 350 nm, and the hexagonal diffraction pattern and thickness contours of the G flakes from transmission electron microscopy confirm ≤ five layers of G. Thermal conductivity of the colloid shows an approximate 17% enhancement for a volume fraction of less than approximately 0.00005 of G. Thus, through the use of CL, this new material and process may improve the use of G in terms of biocompatibility for numerous medical applications that currently employ G, such as internally controlled drug-delivery assisted thermal ablation of carcinoma cells. PMID:24648728

Colloidal graphite/graphene nanostructures using collagen showing enhanced thermal conductivity.

Science.gov (United States)

Bhattacharya, Soumya; Dhar, Purbarun; Das, Sarit K; Ganguly, Ranjan; Webster, Thomas J; Nayar, Suprabha

2014-01-01

In the present study, the exfoliation of natural graphite (GR) directly to colloidal GR/graphene (G) nanostructures using collagen (CL) was studied as a safe and scalable process, akin to numerous natural processes and hence can be termed "biomimetic". Although the exfoliation and functionalization takes place in just 1 day, it takes about 7 days for the nano GR/G flakes to stabilize. The predominantly aromatic residues of the triple helical CL forms its own special micro and nanoarchitecture in acetic acid dispersions. This, with the help of hydrophobic and electrostatic forces, interacts with GR and breaks it down to nanostructures, forming a stable colloidal dispersion. Surface enhanced Raman spectroscopy, X-ray diffraction, photoluminescence, fluorescence, and X-ray photoelectron spectroscopy of the colloid show the interaction between GR and CL on day 1 and 7. Differential interference contrast images in the liquid state clearly reveal how the GR flakes are entrapped in the CL fibrils, with a corresponding fluorescence image showing the intercalation of CL within GR. Atomic force microscopy of graphene-collagen coated on glass substrates shows an average flake size of 350 nm, and the hexagonal diffraction pattern and thickness contours of the G flakes from transmission electron microscopy confirm ≤ five layers of G. Thermal conductivity of the colloid shows an approximate 17% enhancement for a volume fraction of less than approximately 0.00005 of G. Thus, through the use of CL, this new material and process may improve the use of G in terms of biocompatibility for numerous medical applications that currently employ G, such as internally controlled drug-delivery assisted thermal ablation of carcinoma cells.

Heteroaggregation of titanium dioxide nanoparticles with natural clay colloids.

Science.gov (United States)

Labille, Jérôme; Harns, Carrie; Bottero, Jean-Yves; Brant, Jonathan

2015-06-02

To better understand and predict the fate of engineered nanoparticles in the water column, we assessed the heteroaggregation of TiO2 nanoparticles with a smectite clay as analogues for natural colloids. Heteroaggregation was evaluated as a function of water salinity (10(-3) and 10(-1) M NaCl), pH (5 and 8), and selected nanoparticle concentration (0-4 mg/L). Time-resolved laser diffraction was used, coupled to an aggregation model, to identify the key mechanisms and variables that drive the heteroaggregation of the nanoparticles with colloids. Our data show that, at a relevant concentration, nanoparticle behavior is mainly driven by heteroaggregation with colloids, while homoaggregation remains negligible. The affinity of TiO2 nanoparticles for clay is driven by electrostatic interactions. Opposite surface charges and/or high ionic strength favored the formation of primary heteroaggregates via the attachment of nanoparticles to the clay. The initial shape and dispersion state of the clay as well as the nanoparticle/clay concentration ratio also affected the nature of the heteroaggregation mechanism. With dispersed clay platelets (10(-3) M NaCl), secondary heteroaggregation driven by bridging nanoparticles occurred at a nanoparticle/clay number ratio of greater than 0.5. In 10(-1) M NaCl, the clay was preaggregated into larger and more spherical units. This favored secondary heteroaggregation at lower nanoparticle concentration that correlated to the nanoparticle/clay surface area ratio. In this latter case, a nanoparticle to clay sticking efficiency could be determined.

EDITORIAL: Colloidal suspensions Colloidal suspensions

Science.gov (United States)

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

2011-05-01

fluid-fluid interface [2]. Together with Remco Tuinier, Henk has recently completed a book in this area which is to appear later this year. A major theme in Henk's research is that of phase transitions in lyotropic liquid crystals. Henk, together with Daan Frenkel and Alain Stroobants, realized in the 1980s that a smectic phase in dispersions of rod-like particles can be stable without the presence of attractive interactions, similar to nematic ordering as predicted earlier by Onsager [3]. Together with Gert-Jan Vroege he wrote a seminal review in this area [4]. Henk once said that 'one can only truly develop one colloidal model system in one's career' and in his case this must be that of gibbsite platelets. Initially Henk's group pursued another polymorph of aluminium hydroxide, boehmite, which forms rod-like particles [5], which already displayed nematic liquid crystal phases. The real breakthrough came when the same precursors treated the produced gibbsite platelets slightly differently. These reliably form a discotic nematic phase [6] and, despite the polydispersity in their diameter, a columnar phase [7]. A theme encompassing a wide range of soft matter systems is that of colloidal dynamics and phase transition kinetics. Many colloidal systems have a tendency to get stuck in metastable states, such as gels or glasses. This is a nuisance if one wishes to study phase transitions, but it is of great practical significance. Such issues feature in many of Henk's publications, and with Valerie Anderson he wrote a highly cited review in this area [8]. Henk Lekkerkerker has also invested significant effort into the promotion of synchrotron radiation studies of colloidal suspensions. He was one of the great supporters of the Dutch-Belgian beamline 'DUBBLE' project at the ESRF [9]. He attended one of the very first experiments in Grenoble in 1999, which led to a Nature publication [7]. He was strongly involved in many other experiments which followed and also has been a

Experimental and Numerical Investigations on Colloid-facilitated Plutonium Reactive Transport in Fractured Tuffaceous Rocks

Science.gov (United States)

Dai, Z.; Wolfsberg, A. V.; Zhu, L.; Reimus, P. W.

2017-12-01

Colloids have the potential to enhance mobility of strongly sorbing radionuclide contaminants in fractured rocks at underground nuclear test sites. This study presents an experimental and numerical investigation of colloid-facilitated plutonium reactive transport in fractured porous media for identifying plutonium sorption/filtration processes. The transport parameters for dispersion, diffusion, sorption, and filtration are estimated with inverse modeling for minimizing the least squares objective function of multicomponent concentration data from multiple transport experiments with the Shuffled Complex Evolution Metropolis (SCEM). Capitalizing on an unplanned experimental artifact that led to colloid formation and migration, we adopt a stepwise strategy to first interpret the data from each experiment separately and then to incorporate multiple experiments simultaneously to identify a suite of plutonium-colloid transport processes. Nonequilibrium or kinetic attachment and detachment of plutonium-colloid in fractures was clearly demonstrated and captured in the inverted modeling parameters along with estimates of the source plutonium fraction that formed plutonium-colloids. The results from this study provide valuable insights for understanding the transport mechanisms and environmental impacts of plutonium in fractured formations and groundwater aquifers.

Mobilization And Characterization Of Colloids Generated From Cement Leachates Moving Through A SRS Sandy Sediment

International Nuclear Information System (INIS)

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

2011-01-01

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

Dispersions of silica nanoparticles in ionic liquids investigated with advanced rheology

International Nuclear Information System (INIS)

Wittmar, Alexandra; Ruiz-Abad, David; Ulbricht, Mathias

2012-01-01

The colloidal stabilities of dispersions of unmodified and surface-functionalized SiO 2 nanoparticles in hydrophobic and hydrophilic imidazolium-based ionic liquids were studied with advanced rheology at three temperatures (25, 100, and 200 °C). The rheological behavior of the dispersions was strongly affected by the ionic liquids hydrophilicity, by the nanoparticles surface, by the concentration of the nanoparticles in the dispersion as well as by the temperature. The unmodified hydrophilic nanoparticles showed a better compatibility with the hydrophilic ionic liquid. The SiO 2 surface functionalization with hydrophobic groups clearly improved the colloidal stability of the dispersions in the hydrophobic ionic liquid. The temperature increase was found to lead to a destabilization in all studied systems, especially at higher concentrations. The results of this study imply that ionic liquids with tailored properties could be used in absorbers directly after reactors for gas-phase synthesis of nanoparticles or/and as solvents for their further surface functionalization without agglomeration or aggregation.

Reductive and oxidative reactions with inorganic colloids in aqueous solution initiated by ultrasound

International Nuclear Information System (INIS)

Mulvaney, P.C.; Sostaric, J.Z.; Ashokkumar, M.; Grieser, F.

1998-01-01

Full text: The absorption of ultrasound in an aqueous solution can lead to the formation of H and OH radicals which can act as redox species or react with solutes to produce secondary radicals which themselves may participate in electron transfer reactions. The radical formation occurs through the growth then rapid collapse of microbubbles a process that produces localised hot spots with an internal temperature of the order of 5000 K. We have examined two colloidal systems one involving the reductive dissolution of MnO 2 colloids and the other the oxidative dissolution of CdS colloids. In the case of MnO 2 dissolution we found that the reduction of the colloidal metal oxide was considerably enhanced in the presence of aliphatic alcohols in solution and the longer the alkyl chain length on the alcohol the greater its effect. The dissolution of CdS colloids which we ascribe to the reaction of H 2 O 2 and O 2 - with the metal sulfide lo yield Cd 2+ and S could be significantly retarded by the presence of excess S 2- in solution. The mechanisms involved in these two dissolution processes will he presented. Our results clearly show that sonochemical reactions are quite efficient in colloidal solutions and this fact needs to be considered when using sonication to disperse colloidal material in solution, a common practice among colloid chemists

SANS observations on weakly flocculated dispersions

DEFF Research Database (Denmark)

Mischenko, N.; Ourieva, G.; Mortensen, K.

1997-01-01

Structural changes occurring in colloidal dispersions of poly-(methyl metacrylate) (PMMA) particles, sterically stabilized with poly-(12-hydroxystearic acid) (PHSA), while varying the solvent quality, temperature and shear rate, are investigated by small-angle neutron scattering (SANS......). For a moderately concentrated dispersion in a marginal solvent the transition on cooling from the effective stability to a weak attraction is monitored, The degree of attraction is determined in the framework of the sticky spheres model (SSM), SANS and rheological results are correlated....

Long-term kinetic effects and colloid formations in dissolution of LWR spent fuels

Energy Technology Data Exchange (ETDEWEB)

Ahn, T.M.

1996-11-01

This report evaluates continuous dissolution and colloid formation during spent-fuel performance under repository conditions in high-level waste disposal. Various observations suggest that reprecipitated layers formed on spent-fuel surfaces may not be protective. This situation may lead to continuous dissolution of highly soluble radionuclides such as C-14, Cl-36, Tc-99, I-129, and Cs-135. However, the diffusion limits of various species involved may retard dissolution significantly. For low-solubility actinides such as Pu-(239+240) or Am-(241+243), various processes regarding colloid formation have been analyzed. The processes analyzed are condensation, dispersion, and sorption. Colloid formation may lead to significant releases of low-solubility actinides. However, because there are only limited data available on matrix dissolution, colloid formation, and solubility limits, many uncertainties still exist. These uncertainties must be addressed before the significance of radionuclide releases can be determined. 118 refs.

Long-term kinetic effects and colloid formations in dissolution of LWR spent fuels

International Nuclear Information System (INIS)

Ahn, T.M.

1996-11-01

This report evaluates continuous dissolution and colloid formation during spent-fuel performance under repository conditions in high-level waste disposal. Various observations suggest that reprecipitated layers formed on spent-fuel surfaces may not be protective. This situation may lead to continuous dissolution of highly soluble radionuclides such as C-14, Cl-36, Tc-99, I-129, and Cs-135. However, the diffusion limits of various species involved may retard dissolution significantly. For low-solubility actinides such as Pu-(239+240) or Am-(241+243), various processes regarding colloid formation have been analyzed. The processes analyzed are condensation, dispersion, and sorption. Colloid formation may lead to significant releases of low-solubility actinides. However, because there are only limited data available on matrix dissolution, colloid formation, and solubility limits, many uncertainties still exist. These uncertainties must be addressed before the significance of radionuclide releases can be determined. 118 refs

Conducting polymer colloids, hydrogels, and cryogels: common start to various destinations

Czech Academy of Sciences Publication Activity Database

Stejskal, Jaroslav; Bober, Patrycja

2018-01-01

Roč. 296, č. 5 (2018), s. 989-994 ISSN 0303-402X R&D Projects: GA ČR(CZ) GA16-02787S Institutional support: RVO:61389013 Keywords : conducting polymer * polyaniline * colloidal dispersion Subject RIV: CD - Macromolecular Chemistry OBOR OECD: Polymer science Impact factor: 1.723, year: 2016

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

Experimental and Theoretical Investigations on Agglomeration of Magnetic Colloidal Particles in Magnetic Fluids

Science.gov (United States)

Taketomi, Susamu; Takahashi, Hiromasa; Inaba, Nobuyuki; Miyajima, Hideki

1991-05-01

Macro-clusters formation of the magnetic colloidal particles in magnetic fluids is investigated. Experiments of an optical microscope observation of the macro-clusters formation and of anomalous light scattering by the magnetic fluid are reported. Looking upon the anomalous light scattering of the magnetic fluid as a kind of critical opalescence and using Debye’s opalescence theory, we derive a thermodynamical instability theory of the colloidal particles’ dispersion. Relations among the instability theory of Cebers, that of Sano and Doi, and ours are discussed. An interaction energy among the colloidal particles is evaluated from the light scattering experiment. Similarities among the macro-cluster formation, spinodal decomposition of precipitation-type magnetic alloys, and flux-line lattice formation in type-II superconductors are discussed.

Colloid Release From Differently Managed Loess Soil

DEFF Research Database (Denmark)

Vendelboe, Anders Lindblad; Schjønning, Per; Møldrup, Per

2012-01-01

The content of water-dispersible colloids (WDC) in a soil can have a major impact on soil functions, such as permeability to water and air, and on soil strength, which can impair soil fertility and workability. In addition, the content of WDC in the soil may increase the risk of nutrient loss...... and of colloid-facilitated transport of strongly sorbing compounds. In the present study, soils from the Bad Lauchsta¨dt longterm static fertilizer experiment with different management histories were investigated to relate basic soil properties to the content of WDC, the content of water-stable aggregates (WSA......), and aggregate tensile strength. Our studies were carried out on soils on identical parent material under controlled management conditions, enabling us to study the long-term effects on soil physical properties with few explanatory variables in play. The content of WDC and the amount of WSA were measured...

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

Spatial and Temporal Variability in Colloid Dispersion as a Function of Groundwater Injection Rate within Atlantic Coastal Plain Sediments

International Nuclear Information System (INIS)

Seaman, J.C.; P.M. Bertsch and D.I. Kaplan

2007-01-01

A subsurface injection experiment was conducted on the USDOE's Savannah River Site (SRS) to determine the influence of pump-and-treat remediation activities on the generation and transport of groundwater colloids. The impact of colloid generation on formation permeability at injection rates ranging from 19 to 132 L min -1 was monitored using a set of six sampling wells radially spaced at approximate distances of 2.0, 3.0, and 4.5 m from a central injection well. Each sampling well was further divided into three discrete sampling depths that were pumped continuously at a rate of ∼0.1 L min -1 throughout the course of the injection experiment. Discrete samples were collected for turbidity and chemical analysis. Turbidity varied greatly between sampling wells and zones within a given well, ranging from 1 (micro)m) to be readily mobile within the formation. Turbidity measurements taken during this study indicate that colloid mobilization induced by water injection was both spatially and temporally heterogeneous. Furthermore, colloid release did not follow simple predictions based on shear force, presumably due to the complexities encountered in real heterogeneous systems. These findings have important implications to our understanding of how colloids and the co-contaminants are mobilized in the subsurface environment, as well as for the development of monitoring practices that minimize the creation of colloidal artifacts. Technical and logistical obstacles encountered in conducting such an extensive field experiment are also discussed

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

Solid colloidal particles inducing coalescence in bitumen-in-water emulsions.

Science.gov (United States)

Legrand, J; Chamerois, M; Placin, F; Poirier, J E; Bibette, J; Leal-Calderon, F

2005-01-04

Silica particles are dispersed in the continuous phase of bitumen-in-water emulsions. The mixture remains dispersed in quiescent storage conditions. However, rapid destabilization occurs once a shear is applied. Observations under the microscope reveal that the bitumen droplets form a colloidal gel and coalesce upon application of a shear. We follow the kinetic evolution of the emulsions viscosity, eta, at constant shear rate: eta remains initially constant and exhibits a dramatic increase after a finite time, tau. We study the influence of various parameters on the evolution of tau: bitumen droplet size and volume fraction, silica diameter and concentration, shear rate, etc.

Building micro-soccer-balls with evaporating colloidal fakir drops

Science.gov (United States)

Gelderblom, Hanneke; Marín, Álvaro G.; Susarrey-Arce, Arturo; van Housselt, Arie; Lefferts, Leon; Gardeniers, Han; Lohse, Detlef; Snoeijer, Jacco H.

2013-11-01

Drop evaporation can be used to self-assemble particles into three-dimensional microstructures on a scale where direct manipulation is impossible. We present a unique method to create highly-ordered colloidal microstructures in which we can control the amount of particles and their packing fraction. To this end, we evaporate colloidal dispersion drops from a special type of superhydrophobic microstructured surface, on which the drop remains in Cassie-Baxter state during the entire evaporative process. The remainders of the drop consist of a massive spherical cluster of the microspheres, with diameters ranging from a few tens up to several hundreds of microns. We present scaling arguments to show how the final particle packing fraction of these balls depends on the drop evaporation dynamics, particle size, and number of particles in the system.

A re-circulated toxicity exposure chamber to evaluate hydrocarbon dispersions

International Nuclear Information System (INIS)

Fuller, C.B.; Bonner, J.S.; Bujnoch, J.D.; Ussery, S.F.; Arrambide, G.; Sterling, M.C.

2002-01-01

Traditional toxicology methods are not suitable for evaluating chemically dispersed oil which exists mostly as a colloidal suspension and as dissolved fractions. A new toxicity exposure chamber was designed with separate chambers for scaled mixing and organism exposure. The design of the chamber incorporates continuous recirculation between the mixing and exposure chamber and an upward flow in the exposure chamber. The toxicity exposure system incorporates scalable and quantitative mixing inputs with real time particle size analysis and traditional petrochemistry methods to characterize the exposure regime. Changes in dispersion were successfully translated to the organism exposure regime. The study determined the petroleum toxicity with a juvenile marine test species. Low control mortality demonstrated the usefulness of the method for testing toxicity of colloidal oil suspensions. 20 refs., 1 tab., 4 figs

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

Adsorption of polyelectrolytes and charged block copolymers on oxides consequences for colloidal stability

NARCIS (Netherlands)

Hoogeveen, N.G.

1996-01-01

The aim of the study described in this thesis was to examine the adsorption properties of polyelectrolytes and charged block copolymers on oxides, and the effect of these polymers on the colloidal stability of oxidic dispersions. For this purpose the interaction of some well-characterised

Shape-tailored polymer colloids on the road to become structural motifs for hierarchically organized materials.

Science.gov (United States)

Plüisch, Claudia Simone; Wittemann, Alexander

2013-12-01

Anisometric polymer colloids are likely to behave differently when compared with centrosymmetric particles. Their study may not only shine new light on the organization of matter; they may also serve as building units with specific symmetries and complexity to build new materials from them. Polymer colloids of well-defined complex geometries can be obtained by packing a limited number of spherical polymer particles into clusters with defined configurations. Such supracolloidal architectures can be fabricated at larger scales using narrowly dispersed emulsion droplets as templates. Assemblies built from at least two different types of particles as elementary building units open perspectives in selective targeting of colloids with specific properties, aiming for mesoscale building blocks with tailor-made morphologies and multifunctionality. Polymer colloids with defined geometries are also ideal to study shape-dependent properties such as the diffusion of complex particles. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

pH Triggered Recovery and Reuse of Thiolated Poly(acrylic acid) Functionalized Gold Nanoparticles with Applications in Colloidal Catalysis.

Science.gov (United States)

Ansar, Siyam M; Fellows, Benjamin; Mispireta, Patrick; Mefford, O Thompson; Kitchens, Christopher L

2017-08-08

Thiolated poly(acrylic acid) (PAA-SH) functionalized gold nanoparticles were explored as a colloidal catalyst with potential application as a recoverable catalyst where the PAA provides pH-responsive dispersibility and phase transfer capability between aqueous and organic media. This system demonstrates complete nanoparticle recovery and redispersion over multiple reaction cycles without changes in nanoparticle morphology or reduction in conversion. The catalytic activity (rate constant) was reduced in subsequent reactions when recovery by aggregation was employed, despite unobservable changes in morphology or dispersibility. When colloidal catalyst recovery employed a pH induced phase transfer between two immiscible solvents, the catalytic activity of the recovered nanoparticles was unchanged over four cycles, maintaining the original rate constant and 100% conversion. The ability to recover and reuse colloidal catalysts by aggregation/redispersion and phase transfer methods that occur at low and high pH, respectively, could be used for different gold nanoparticle catalyzed reactions that occur at different pH conditions.

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

Formation of Polyelectrolyte Complex Colloid Particles between Chitosan and Pectin with Different Degree of Esterification

Science.gov (United States)

Wang, Hui; Sun, Hongyuan; He, Jieyu

2017-12-01

The effects of degree of esterification, pectin/chitosan ratio and pH on the formation of polyelectrolyte complex colloid particles between chitosan (CS) and pectin (PE) were investigated. Low methoxyl pectin (LPE) was achieved by de-esterifying high methoxyl pectin (HPE) with pectin methyl esterase. Turbidity titration and colorimetric method was used to determine the stability of complex colloid particles. The structure and morphology of complex particles were characterized by FTIR and TEM. When pectin solution was dropped into chitosan solution, complex colloidal dispersion was stable as PE/CS mass ratio was no more than 3:2. Colloidal particles of HPE-CS complex coagulated at larger ratio of PE/CS than LPE-CS. The maximum complex occurred at pH 6.1 for HPE-CS and pH 5.7 for LPE-CS, and decreasing pH leaded to the dissociation of complex particles. Electrostatic interactions between carboxyl groups on pectin and amino groups on chitosan were confirmed by FTIR. Colloidal particle sizes ranged from about 100 nm to 400 nm with spherical shape.

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

A binomial modeling approach for upscaling colloid transport under unfavorable conditions: Emergent prediction of extended tailing

Science.gov (United States)

Hilpert, Markus; Rasmuson, Anna; Johnson, William P.

2017-07-01

Colloid transport in saturated porous media is significantly influenced by colloidal interactions with grain surfaces. Near-surface fluid domain colloids experience relatively low fluid drag and relatively strong colloidal forces that slow their downgradient translation relative to colloids in bulk fluid. Near-surface fluid domain colloids may reenter into the bulk fluid via diffusion (nanoparticles) or expulsion at rear flow stagnation zones, they may immobilize (attach) via primary minimum interactions, or they may move along a grain-to-grain contact to the near-surface fluid domain of an adjacent grain. We introduce a simple model that accounts for all possible permutations of mass transfer within a dual pore and grain network. The primary phenomena thereby represented in the model are mass transfer of colloids between the bulk and near-surface fluid domains and immobilization. Colloid movement is described by a Markov chain, i.e., a sequence of trials in a 1-D network of unit cells, which contain a pore and a grain. Using combinatorial analysis, which utilizes the binomial coefficient, we derive the residence time distribution, i.e., an inventory of the discrete colloid travel times through the network and of their probabilities to occur. To parameterize the network model, we performed mechanistic pore-scale simulations in a single unit cell that determined the likelihoods and timescales associated with the above colloid mass transfer processes. We found that intergrain transport of colloids in the near-surface fluid domain can cause extended tailing, which has traditionally been attributed to hydrodynamic dispersion emanating from flow tortuosity of solute trajectories.

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

Transport of a Two-Member Decay Chain of Radionuclides Through a Discrete Fracture in a Porous Rock Matrix in the Presence of Colloids

International Nuclear Information System (INIS)

Tien, N.-C.; Li Shihhai

2002-01-01

Many physical and chemical processes dominate the transport of radionuclides in groundwater. Among these processes, the decay chain process of radionuclides was frequently disregarded in previous research. However, the daughter products may travel much farther than their parents along the fracture. Therefore, some models neglecting the effect of the decay chain may underestimate the transport radionuclide concentration in geological media. The transport of radionuclides in groundwater is also controlled by colloidal particles. The radionuclides may be enhanced or retarded by the colloids, according to the mobility of these colloidal particles. This work describes a novel model of the transport of a two-member decay chain of radionuclides through a discrete fracture in a porous rock matrix in the presence of colloids. The model addresses the following processes: (a) advective transport in the fracture, (b) mechanical dispersion and molecular diffusion along the fracture, (c) molecular diffusion from the fracture to the rock matrix, (d) adsorption onto the fracture wall, (e) adsorption in the rock matrix, and (f) radioactive decay. Furthermore, colloids are assumed to be excluded from the matrix pores because of their size. A fully developed concentration profile system with nonreactive colloids is used to understand the effect of colloidal sizes by using hydrodynamic chromatography. The external forces acting on the colloid surface, such as the inertial, the van der Waals attractive force, the double layer force, and the gravitational force are accounted for. The parameters, the average velocity of the colloid, the dispersion coefficient of the colloid, and the distribution coefficient of radionuclides with colloids are modified according to the colloidal size. The transport equations for the parent radionuclides are solved analytically using the Laplace transformation and inversion method. However, for the transformed solution of the daughter products along the

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.

Polymer depletion-driven cluster aggregation and initial phase separation in charged nanosized colloids

Science.gov (United States)

Gögelein, Christoph; Nägele, Gerhard; Buitenhuis, Johan; Tuinier, Remco; Dhont, Jan K. G.

2009-05-01

We study polymer depletion-driven cluster aggregation and initial phase separation in aqueous dispersions of charge-stabilized silica spheres, where the ionic strength and polymer (dextran) concentration are systematically varied, using dynamic light scattering and visual observation. Without polymers and for increasing salt and colloid content, the dispersions become increasingly unstable against irreversible cluster formation. By adding nonadsorbing polymers, a depletion-driven attraction is induced, which lowers the stabilizing Coulomb barrier and enhances the cluster growth rate. The initial growth rate increases with increasing polymer concentration and decreases with increasing polymer molar mass. These observations can be quantitatively understood by an irreversible dimer formation theory based on the classical Derjaguin, Landau, Verwey, and Overbeek pair potential, with the depletion attraction modeled by the Asakura-Oosawa-Vrij potential. At low colloid concentration, we observe an exponential cluster growth rate for all polymer concentrations considered, indicating a reaction-limited aggregation mechanism. At sufficiently high polymer and colloid concentrations, and lower salt content, a gas-liquidlike demixing is observed initially. Later on, the system separates into a gel and fluidlike phase. The experimental time-dependent state diagram is compared to the theoretical equilibrium phase diagram obtained from a generalized free-volume theory and is discussed in terms of an initial reversible phase separation process in combination with irreversible aggregation at later times.

Colloid Transport and Retention

DEFF Research Database (Denmark)

Yuan, Hao; Shapiro, Alexander

2012-01-01

related to historical prospective, synthesis, characterization, theoretical modeling and application of unique class of colloidal materials starting from colloidal gold to coated silica colloid and platinum, titania colloids. This book is unique in its design, content, providing depth of science about...

Silver nanoparticle colloids with γ-cyclodextrin: enhanced stability and Gibbs–Marangoni flow

Energy Technology Data Exchange (ETDEWEB)

Amiri, Setareh; Duroux, Laurent; Larsen, Kim Lambertsen, E-mail: kll@bio.aau.dk [Aalborg University, Department of Chemistry and Bioscience (Denmark)

2015-01-15

Although cyclodextrins (CD) are effective stabilizers for metal nanoparticle colloids, differences between α-, β- and γ-CD in stabilizing such colloids have not been previously reported. In this study, silver nanoparticles (AgNP) were synthesized using NaBH{sub 4} as reducing agent and cyclodextrins as stabilizers. Long-term stability of AgNP colloids in equilibrium conditions showed no marked differences between CD types. Transmission electron microscopy and quantitative image analysis revealed only marginal differences in particle sizes for CD-AgNP, although statistically significant. CD-AgNP colloids showed dispersed particles with average diameters of 7.3 ± 2.2, 6.3 ± 2.9 and 4.9 ± 1.9 nm for α-, β- and γ-CD, respectively, and with similar ζ-potentials about −25 to −30 mV. AgNP without CD showed bigger and aggregated particles of 15.0 ± 2.0 nm with lower ζ-potentials of about −40 mV. When subjected to centrifugal forces, i.e. non-equilibrium conditions, γ-CD was markedly more efficient than α- and β-CD in stabilizing the colloids. Drying patterns of colloid droplets showed a typical self-pinned coffee ring for all but the colloid stabilized by γ-CD, which showed a pattern resulting from a dominant Gibbs–Marangoni flow inside the drying droplet. Calculations using the Derjaguin, Landau, Verwey and Overbeek (DLVO) theory supported the stabilizing effect of CD in equilibrium conditions; it however did not provide clues for the superior stabilization by γ-CD in conditions of hydrodynamic stress.

Silver nanoparticle colloids with γ-cyclodextrin: enhanced stability and Gibbs–Marangoni flow

International Nuclear Information System (INIS)

Amiri, Setareh; Duroux, Laurent; Larsen, Kim Lambertsen

2015-01-01

Although cyclodextrins (CD) are effective stabilizers for metal nanoparticle colloids, differences between α-, β- and γ-CD in stabilizing such colloids have not been previously reported. In this study, silver nanoparticles (AgNP) were synthesized using NaBH 4 as reducing agent and cyclodextrins as stabilizers. Long-term stability of AgNP colloids in equilibrium conditions showed no marked differences between CD types. Transmission electron microscopy and quantitative image analysis revealed only marginal differences in particle sizes for CD-AgNP, although statistically significant. CD-AgNP colloids showed dispersed particles with average diameters of 7.3 ± 2.2, 6.3 ± 2.9 and 4.9 ± 1.9 nm for α-, β- and γ-CD, respectively, and with similar ζ-potentials about −25 to −30 mV. AgNP without CD showed bigger and aggregated particles of 15.0 ± 2.0 nm with lower ζ-potentials of about −40 mV. When subjected to centrifugal forces, i.e. non-equilibrium conditions, γ-CD was markedly more efficient than α- and β-CD in stabilizing the colloids. Drying patterns of colloid droplets showed a typical self-pinned coffee ring for all but the colloid stabilized by γ-CD, which showed a pattern resulting from a dominant Gibbs–Marangoni flow inside the drying droplet. Calculations using the Derjaguin, Landau, Verwey and Overbeek (DLVO) theory supported the stabilizing effect of CD in equilibrium conditions; it however did not provide clues for the superior stabilization by γ-CD in conditions of hydrodynamic stress

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

Proceedings of the fifth Asian conference on colloid and interface science

International Nuclear Information System (INIS)

2013-01-01

Colloid and Interfacial (Surface) phenomena constitute a field of science which today embodies concepts that are fundamental to the understanding of both microscopic and macroscopic behaviors, and hence the design of a wide range of system of great potential interest. Now a days, this branch of science has entered a new era where modern development and knowledge of physics, chemistry, biology, material science, pharmacy, engineering, etc., have been extensively exploited and adopted. As a result, both fundamental and applied aspects of colloid and surface science have advanced over the years, for example, starting from tertiary oil recovery to nanotechnology to environmental science. These multifaceted fields also find applications in everyday life, and helps in understanding the intricacies of the life process. All these developments have enriched the field, which is considered to be the front-line/emerging area of research in the national and international scenario. Recent growth of modern colloid and interface science in Asian countries has encouraged the scientists to share in-depth discussions within the regional scientific community in Asia. Scientific topics covered by the conference were: Adsorption, Molecular Assemblies, Colloids and Dispersions, Gels, Surfaces and Interfaces, Thin Films, Membranes, Nanomaterials, Biomaterials, Devices and Applications etc. Papers relevant to INIS are indexed separately

Soft colloidal probes for AFM force measurements between water droplets in oil

KAUST Repository

Vakarelski, Ivan Uriev; Li, Erqiang; Thoroddsen, Sigurdur T

2014-01-01

Here we introduce an extension of the atomic force microscopy (AFM) colloidal probe technique, as a simple and reliable experimental approach to measure the interaction forces between small water droplets (~80-160. μm) dispersed in oil. Small water droplets are formed by capillary breakup of a microscale water jet in air, which is forced out of a fine capillary nozzle, and deposited on a superhydrophobic substrate immersed in tetradecane oil medium. In these conditions the water droplets are very loosely attached to the superhydrophobic substrate and are easily picked up with a hydrophobic AFM cantilever to form a soft colloidal probe. Sample force measurements are conducted to demonstrate the capability of the technique.

Soft colloidal probes for AFM force measurements between water droplets in oil

KAUST Repository

Vakarelski, Ivan Uriev

2014-11-01

Here we introduce an extension of the atomic force microscopy (AFM) colloidal probe technique, as a simple and reliable experimental approach to measure the interaction forces between small water droplets (~80-160. μm) dispersed in oil. Small water droplets are formed by capillary breakup of a microscale water jet in air, which is forced out of a fine capillary nozzle, and deposited on a superhydrophobic substrate immersed in tetradecane oil medium. In these conditions the water droplets are very loosely attached to the superhydrophobic substrate and are easily picked up with a hydrophobic AFM cantilever to form a soft colloidal probe. Sample force measurements are conducted to demonstrate the capability of the technique.

Saturated Zone Colloid Transport

International Nuclear Information System (INIS)

H. S. Viswanathan

2004-01-01

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

Towards vibrational spectroscopy on surface-attached colloids performed with a quartz crystal microbalance

Directory of Open Access Journals (Sweden)

Diethelm Johannsmann

2016-12-01

Full Text Available Colloidal spheres attached to a quartz crystal microbalance (QCM produce the so-called “coupled resonances”. They are resonators of their own, characterized by a particle resonance frequency, a resonance bandwidth, and a modal mass. When the frequency of the main resonator comes close to the frequency of the coupled resonance, the bandwidth goes through a maximum. A coupled resonance can be viewed as an absorption line in acoustic shear-wave spectroscopy. The known concepts from spectroscopy apply. This includes the mode assignment problem, selection rules, and the oscillator strength. In this work, the mode assignment problem was addressed with Finite Element calculations. These reveal that a rigid sphere in contact with a QCM displays two modes of vibration, termed “slipping” and “rocking”. In the slipping mode, the sphere rotates about its center; it exerts a tangential force onto the resonator surface at the point of contact. In the rocking mode, the sphere rotates about the point of contact; it exerts a torque onto the substrate. In liquids, both axes of rotation are slightly displaced from their ideal positions. Characteristic for spectroscopy, the two modes do not couple to the mechanical excitation equally well. The degree of coupling is quantified by an oscillator strength. Because the rocking mode mostly exerts a torque (rather than a tangential force, its coupling to the resonator's tangential motion is weak; the oscillator strength consequently is small. Recent experiments on surface-adsorbed colloidal spheres can be explained by the mode of vibration being of the rocking type. Keywords: Quartz crystal microbalance, Coupled resonance, Biocolloids, Adsorption

Colloid chemistry: available sorption models and the question of colloid adhesion

International Nuclear Information System (INIS)

Grauer, R.

1990-05-01

A safety analysis of a radioactive waste repository should consider the possibility of nuclide transport by colloids. This would involve describing the sorption properties of the colloids and their transport in porous and fissured media. This report deals with a few selected aspects of the chemistry of this complex subject. Because the mechanisms of ion adsorption onto surfaces are material-specific, increased attention should be paid to identifying the material constitution of aquatic colloids. Suitable models already exist for describing reversible adsorption; these models describe sorption using mass action equations. The surface coordination model, developed for hydrous oxide surfaces, allows a uniform approach to be adopted for different classes of materials. This model is also predictive and has been applied successfully to natural systems. From the point of view of nuclide transport by colloids, irreversible sorption represents the most unfavourable situation. There is virtually no information available on the extent of reversibility and on the desorption kinetics of important nuclide/colloid combinations. Experimental investigations are therefore necessary in this respect. The only question considered in connection with colloid transport and its modelling is that of colloid sticking. Natural colloids, and the surfaces of the rock on which they may be collected, generally have negative surface charges so that colloid sticking will be difficult. The DLVO theory contains an approach for calculating the sticking factor from the surface potentials of the solid phases and the ionic strength of the water. However, it has been shown that this theory is inapplicable because of inherent shortcomings which lead to completely unrealistic predictions. The sticking probability of colloids should therefore be determined experimentally for systems which correspond as closely as possible to reality. (author) 66 figs., 12 tabs., 204 refs

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.

Synthesis of Ag-coated polystyrene colloids by an improved surface seeding and shell growth technique

International Nuclear Information System (INIS)

Tian Chungui; Wang Enbo; Kang Zhenhui; Mao Baodong; Zhang Chao; Lan Yang; Wang Chunlei; Song Yanli

2006-01-01

In this paper, an improved surface seeding and shell growth technique was developed to prepare Ag-polystyrene core shell composite. Polyethyleneimine (PEI) could act as the linker between Ag ions (Ag nanoparticles) and polystyrene (PS) colloids and the reducing agent in the formation of Ag nanoparticles. Due to the multi-functional characteristic of PEI, Ag seeds formed in-situ and were immobilized on the surface of PEI-modified PS colloids and no free Ag clusters coexist with the Ag 'seeding' PS colloids in the system. Then, the additional agents could be added into the resulting dispersions straightly to produce a thick Ag nanoshell. The Ag nanoshell with controllable thickness was formed on the surface of PS by the 'one-pot' surface seeding and shell growth method. The Ag-coverage increased gradually with the increasing of mass ratio of AgNO 3 /PS. The optical properties of the Ag-PS colloids could be tailored by changing the coverage of Ag. - Graphical abstract: An improved surface seeding and shell growth technique was developed to prepare Ag-polystyrene core shell composite. The optical properties of the Ag-PS colloids could be tailored by changing the coverage of Ag. Display Omitted

COLLAGE 2: a numerical code for radionuclide migration through a fractured geosphere in aqueous and colloidal phases

International Nuclear Information System (INIS)

Grindrod, P.; Cooper, N.

1993-05-01

In previous work, the COLLAGE code was developed to model the impacts of mobile and immobile colloidal material upon the dispersal and migration of a radionuclide species within a saturated planer fracture surrounded by porous media. The adsorption of radionuclides to colloid surfaces was treated as instantaneous and reversible. In this report we present a new version of the code, COLLAGE 2. Here the adsorption of radionuclides to the colloidal material is treated via first order kinetics. The flow and geometry of the fracture remain as in the previous model. The major effect of colloids upon the radionuclide species is to adsorb them within the fracture space and thus exclude them from the surrounding porous medium. Thus the matrix diffusion process, a strongly retarding effect, is exchanged for a colloid capture/release process by which adsorbed nuclides are also retarded. The effects of having a colloid-radionuclide kinetic interaction include the phenomena of double pulse breakthrough (the pseudo colloid population followed by the solute plume) in cases where the desorption process is slow and the pseudo colloids are highly mobile. Some example calculations are given and some verification examples are discussed. Finally a complete listing of the code is presented as an appendix, including the subroutines allowing for the numerical inversion of the Laplace transformed solution via Talbot's method. 6 figs

COLLAGE 2: a numerical code for radionuclide migration through a fractured geosphere in aqueous and colloidal phases

Energy Technology Data Exchange (ETDEWEB)

Grindrod, P.; Cooper, N. [Intera Information Technologies Ltd., Henley-on-Thames (United Kingdom)

1993-05-01

In previous work, the COLLAGE code was developed to model the impacts of mobile and immobile colloidal material upon the dispersal and migration of a radionuclide species within a saturated planer fracture surrounded by porous media. The adsorption of radionuclides to colloid surfaces was treated as instantaneous and reversible. In this report we present a new version of the code, COLLAGE 2. Here the adsorption of radionuclides to the colloidal material is treated via first order kinetics. The flow and geometry of the fracture remain as in the previous model. The major effect of colloids upon the radionuclide species is to adsorb them within the fracture space and thus exclude them from the surrounding porous medium. Thus the matrix diffusion process, a strongly retarding effect, is exchanged for a colloid capture/release process by which adsorbed nuclides are also retarded. The effects of having a colloid-radionuclide kinetic interaction include the phenomena of double pulse breakthrough (the pseudo colloid population followed by the solute plume) in cases where the desorption process is slow and the pseudo colloids are highly mobile. Some example calculations are given and some verification examples are discussed. Finally a complete listing of the code is presented as an appendix, including the subroutines allowing for the numerical inversion of the Laplace transformed solution via Talbot`s method. 6 figs.

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

Science.gov (United States)

Ueno, Keihei; Kina, Ken'yu

1985-01-01

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

Saturated Zone Colloid Transport

Energy Technology Data Exchange (ETDEWEB)

H. S. Viswanathan

2004-10-07

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

Size-fractionation of groundwater arsenic in alluvial aquifers of West Bengal, India: the role of organic and inorganic colloids.

Science.gov (United States)

Majumder, Santanu; Nath, Bibhash; Sarkar, Simita; Chatterjee, Debashis; Roman-Ross, Gabriela; Hidalgo, Manuela

2014-01-15

Dissolved organic carbon (DOC) and Fe mineral phases are known to influence the mobility of arsenic (As) in groundwater. Arsenic can be associated with colloidal particles containing organic matter and Fe. Currently, no data is available on the dissolved phase/colloidal association of As in groundwater of alluvial aquifers in West Bengal, India. This study investigated the fractional distribution of As (and other metals/metalloids) among the particulate, colloidal and dissolved phases in groundwater to decipher controlling behavior of organic and inorganic colloids on As mobility. The result shows that 83-94% of As remained in the 'truly dissolved' phases (i.e., 0.05 μm size) colloidal particles, which indicates the close association of As with larger Fe-rich inorganic colloids. In smaller (i.e., <0.05 μm size) colloidal particles strong positive correlation is observed between As and DOC (r(2)=0.85), which highlights the close association of As with smaller organic colloids. As(III) is mainly associated with larger inorganic colloids, whereas, As(V) is associated with smaller organic/organometallic colloids. Scanning Electron Microscopy and Energy Dispersive X-ray spectroscopy confirm the association of As with DOC and Fe mineral phases suggesting the formation of dissolved organo-Fe complexes and colloidal organo-Fe oxide phases. Attenuated total reflectance-Fourier transform infrared spectroscopy further confirms the formation of As-Fe-NOM organometallic colloids, however, a detailed study of these types of colloids in natural waters is necessary to underpin their controlling behavior. © 2013 Elsevier B.V. All rights reserved.

Photoinduced charge separation in a colloidal system of exfoliated layered semiconductor controlled by coexisting aluminosilicate clay.

Science.gov (United States)

Nakato, Teruyuki; Yamada, Yoshimi; Miyamoto, Nobuyoshi

2009-02-05

We investigated photoinduced charge separation occurring in a multicomponent colloidal system composed of oxide nanosheets of photocatalytically active niobate and photochemically inert clay and electron accepting methylviologen dications (MV2+). The inorganic nanosheets were obtained by exfoliation of layered hexaniobate and hectorite clay. The niobate and clay nanosheets were spatially separated in the colloidally dispersed state, and the MV2+ molecules were selectively adsorbed on the clay platelets. UV irradiation of the colloids led to electron transfer from the niobate nanosheets to the MV2+ molecules adsorbed on clay. The photoinduced electron transfer produced methylviologen radical cations (MV*+), which was characterized by high yield and long lifetime. The yield and stability of the MV*+ species were found to depend strongly on the clay content of the colloid: from a few mol % to approximately 70 mol % of the yield and several tens of minutes to more than 40 h of the lifetime. The contents of the niobate nanosheets and MV2+ molecules and the aging of the colloid also affected the photoinduced charge separation. In the absence of MV2+ molecules in the colloid, UV irradiation induced electron accumulation in the niobate nanosheets. The stability of the electron-accumulated state also depended on the clay content. The variation in the photochemical behavior is discussed in relation to the viscosity of the colloid.

Titanium in UK rural, agricultural and urban/industrial rivers: Geogenic and anthropogenic colloidal/sub-colloidal sources and the significance of within-river retention

International Nuclear Information System (INIS)

Neal, Colin; Jarvie, Helen; Rowland, Philip; Lawler, Alan; Sleep, Darren; Scholefield, Paul

2011-01-01

Operationally defined dissolved Titanium [Ti] (the 1 kDa i.e. > c. 1-2 nm) for the rural areas, but as low as 28% for the urban/industrial rivers. This raises fundamental issues of the pollutant inputs of Ti, with the possibility of significant complexation of Ti in the sewage effluents and subsequent breakdown within the rivers, as well as the physical dispersion of fine colloids down to the macro-molecular scale. Although not directly measured, the particulate Ti can make an important contribution to the net Ti flux. - Research Highlights: → Filtered Ti in agricultural, urban and industrial UK rivers described. → Highest concentrations occur just downstream of STWs. → The urban/industrial inputs increased background [Ti] by up to 11 fold. → Anthropogenic Ti input lowered by within-river retention. → Up to 79% of Ti colloidal/NP for rural, down to 28% for urban/industrial rivers.

Ni(0-CMC-Na Nickel Colloids in Sodium Carboxymethyl-Cellulose: Catalytic Evaluation in Hydrogenation Reactions

Directory of Open Access Journals (Sweden)

Abdallah Karim

2011-01-01

Full Text Available A recyclable catalyst, Ni(0-CMC-Na, composed of nickel colloids dispersed in a water soluble bioorganic polymer, sodium carboxymethylcellulose (CMC-Na, was synthesized by a simple procedure from readily available reagents. The catalyst thus obtained is stable and highly active in alkene hydrogenations.

Long-Ranged Oppositely Charged Interactions for Designing New Types of Colloidal Clusters

Directory of Open Access Journals (Sweden)

Ahmet Faik Demirörs

2015-04-01

Full Text Available Getting control over the valency of colloids is not trivial and has been a long-desired goal for the colloidal domain. Typically, tuning the preferred number of neighbors for colloidal particles requires directional bonding, as in the case of patchy particles, which is difficult to realize experimentally. Here, we demonstrate a general method for creating the colloidal analogs of molecules and other new regular colloidal clusters without using patchiness or complex bonding schemes (e.g., DNA coating by using a combination of long-ranged attractive and repulsive interactions between oppositely charged particles that also enable regular clusters of particles not all in close contact. We show that, due to the interplay between their attractions and repulsions, oppositely charged particles dispersed in an intermediate dielectric constant (4<ϵ<10 provide a viable approach for the formation of binary colloidal clusters. Tuning the size ratio and interactions of the particles enables control of the type and shape of the resulting regular colloidal clusters. Finally, we present an example of clusters made up of negatively charged large and positively charged small satellite particles, for which the electrostatic properties and interactions can be changed with an electric field. It appears that for sufficiently strong fields the satellite particles can move over the surface of the host particles and polarize the clusters. For even stronger fields, the satellite particles can be completely pulled off, reversing the net charge on the cluster. With computer simulations, we investigate how charged particles distribute on an oppositely charged sphere to minimize their energy and compare the results with the solutions to the well-known Thomson problem. We also use the simulations to explore the dependence of such clusters on Debye screening length κ^{−1} and the ratio of charges on the particles, showing good agreement with experimental observations.

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.

Colloid process engineering

CERN Document Server

Peukert, Wolfgang; Rehage, Heinz; Schuchmann, Heike

2015-01-01

This book deals with colloidal systems in technical processes and the influence of colloidal systems by technical processes. It explores how new measurement capabilities can offer the potential for a dynamic development of scientific and engineering, and examines the origin of colloidal systems and its use for new products. The future challenges to colloidal process engineering are the development of appropriate equipment and processes for the production and obtainment of multi-phase structures and energetic interactions in market-relevant quantities. The book explores the relevant processes and for controlled production and how they can be used across all scales.

Third-order nonlinear optical response of colloidal gold nanoparticles prepared by sputtering deposition

Energy Technology Data Exchange (ETDEWEB)

Castro, Hemerson P. S.; Alencar, Márcio A. R. C.; Hickmann, Jandir M. [Optics and Materials Group–OPTMA, Universidade Federal de Alagoas, CAIXA POSTAL 2051, 57061-970 Maceió (Brazil); Wender, Heberton [Brazilian Synchrotron National Laboratory (LNLS), CNPEM, Rua Giuseppe Máximo Scolfaro 10.000, 13083-970 Campinas (Brazil); Department of Physics, Universidade Federal do Mato Grosso do Sul, 79070-900, Campo Grande (Brazil); Teixeira, Sergio R. [Institute of Physics, Universidade Federal do Rio Grande do Sul, 91501-970, Porto Alegre (Brazil); Dupont, Jairton [Laboratory of Molecular Catalysis, Institute of Chemistry, Universidade Federal do Rio Grande do Sul, 91501-970, Porto Alegre (Brazil)

2013-11-14

The nonlinear optical responses of gold nanoparticles dispersed in castor oil produced by sputtering deposition were investigated, using the thermally managed Z-scan technique. Particles with spherical shape and 2.6 nm of average diameter were obtained and characterized by transmission electron microscopy and small angle X-ray scattering. This colloid was highly stable, without the presence of chemical impurities, neither stabilizers. It was observed that this system presents a large refractive third-order nonlinear response and a negligible nonlinear absorption. Moreover, the evaluation of the all-optical switching figures of merit demonstrated that the colloidal nanoparticles prepared by sputtering deposition have a good potential for the development of ultrafast photonic devices.

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.

Origin of blue photoluminescence from colloidal silicon nanocrystals fabricated by femtosecond laser ablation in solution.

Science.gov (United States)

Hao, H L; Wu, W S; Zhang, Y; Wu, L K; Shen, W Z

2016-08-12

We present a detailed investigation into the origin of blue emission from colloidal silicon (Si) nanocrystals (NCs) fabricated by femtosecond laser ablation of Si powder in 1-hexene. High resolution transmission electron microscopy and Raman spectroscopy observations confirm that Si NCs with average size 2.7 nm are produced and well dispersed in 1-hexene. Fourier transform infrared spectrum and x-ray photoelectron spectra have been employed to reveal the passivation of Si NCs surfaces with organic molecules. On the basis of the structural characterization, UV-visible absorption, temperature-dependent photoluminescence (PL), time-resolved PL, and PL excitation spectra investigations, we deduce that room-temperature blue luminescence from colloidal Si NCs originates from the following two processes: (i) under illumination, excitons first form within colloidal Si NCs by direct transition at the X or Γ (Γ25 → Γ'2) point; (ii) and then some trapped excitons migrate to the surfaces of colloidal Si NCs and further recombine via the surface states associated with the Si-C or Si-C-H2 bonds.

Observation particle morphology of colloidal system by conventional SEM with an improved specimen preparation technique.

Science.gov (United States)

Xu, Jing; Hou, Zhaosheng; Yuan, Xiaojiao; Guo, Hong

2011-08-01

On the basis of our previous report that polymer emulsion with different viscosity can be investigated by conventional scanning electron microscopy (SEM), we have developed an improved specimen preparation technique for obtaining particle morphology and size of colloidal silver, collagen, glutin, and polymer microspheres. In this study, we expect to provide a means for charactering the three-dimensional surface microstructure of colloidal particles. Dilution of the samples with appropriate volatile solvent like ethanol is effective for SEM specimen preparation. At a proper ratio between sample and ethanol, the colloidal particles are dispersed uniformly in ethanol and then deposited evenly on the substrate. Different drying methods are studied to search a proper drying condition, in which the small molecule solvent is removed without destroying the natural particle morphology. And the effects of ethanol in the specimen preparation process are described by analyzing the physicochemical properties of ethanol. The specimen preparation technique is simple and can be achieved in common laboratory for charactering the particle morphology of colloidal system. Copyright © 2010 Wiley-Liss, Inc.

Preparation and Optical Properties of Spherical Inverse Opals by Liquid Phase Deposition Using Spherical Colloidal Crystals

International Nuclear Information System (INIS)

Aoi, Y; Tominaga, T

2013-01-01

Titanium dioxide (TiO 2 ) inverse opals in spherical shape were prepared by liquid phase deposition (LPD) using spherical colloidal crystals as templates. Spherical colloidal crystals were produced by ink-jet drying technique. Aqueous emulsion droplets that contain polystyrene latex particles were ejected into air and dried. Closely packed colloidal crystals with spherical shape were obtained. The obtained spherical colloidal crystals were used as templates for the LPD. The templates were dispersed in the deposition solution of the LPD, i.e. a mixed solution of ammonium hexafluorotitanate and boric acid and reacted for 4 h at 30 °C. After the LPD process, the interstitial spaces of the spherical colloidal crystals were completely filled with titanium oxide. Subsequent heat treatment resulted in removal of templates and spherical titanium dioxide inverse opals. The spherical shape of the template was retained. SEM observations indicated that the periodic ordered voids were surrounded by titanium dioxide. The optical reflectance spectra indicated that the optical properties of the spherical titanium dioxide inverse opals were due to Bragg diffractions from the ordered structure. Filling in the voids of the inverse opals with different solvents caused remarkable changes in the reflectance peak.

Effects of confinement and external fields on structure and transport in colloidal dispersions in reduced dimensionality

International Nuclear Information System (INIS)

Wilms, D; Virnau, P; Binder, K; Deutschländer, S; Siems, U; Franzrahe, K; Henseler, P; Keim, P; Schwierz, N; Maret, G; Nielaba, P

2012-01-01

In this work, we focus on low-dimensional colloidal model systems, via simulation studies and also some complementary experiments, in order to elucidate the interplay between phase behavior, geometric structures and transport properties. In particular, we try to investigate the (nonlinear!) response of these very soft colloidal systems to various perturbations: uniform and uniaxial pressure, laser fields, shear due to moving boundaries and randomly quenched disorder. We study ordering phenomena on surfaces or in monolayers by Monte Carlo computer simulations of binary hard-disk mixtures, the influence of a substrate being modeled by an external potential. Weak external fields allow a controlled tuning of the miscibility of the mixture. We discuss the laser induced de-mixing for the three different possible couplings to the external potential. The structural behavior of hard spheres interacting with repulsive screened Coulomb or dipolar interaction in 2D and 3D narrow constrictions is investigated using Brownian dynamics simulations. Due to misfits between multiples of the lattice parameter and the channel widths, a variety of ordered and disordered lattice structures have been observed. The resulting local lattice structures and defect probabilities are studied for various cross sections. The influence of a self-organized order within the system is reflected in the velocity of the particles and their diffusive behavior. Additionally, in an experimental system of dipolar colloidal particles confined by gravity on a solid substrate we investigate the effect of pinning on the dynamics of a two-dimensional colloidal liquid. This work contains sections reviewing previous work by the authors as well as new, unpublished results. Among the latter are detailed studies of the phase boundaries of the de-mixing regime in binary systems in external light fields, configurations for shear induced effects at structured walls, studies on the effect of confinement on the structures

Radioactive colloids

International Nuclear Information System (INIS)

Bergqvist, L.

1987-01-01

Different techniques for the characterization of radioactive colloids, used in nuclear medicine, have been evaluated and compared. Several radioactive colloids have been characterized in vitro and in vivo and tested experimentally. Colloid biokinetics following interstitial or intravenous injection were evaluated with a scintillation camera technique. Lymphoscintigraphy with a Tc-99-labelled antimony sulphur colloid was performed in 32 patients with malignant melanoma in order to evaluate the technique. Based on the biokinetic results, absorbed doses in tissues and organs were calculated. The function of the reticuloendothelial system has been evaluated in rats after inoculation with tumour cells. Microfiltration and photon correlation spectroscopy were found to be suitable in determining activity-size and particle size distributions, respectively. Maximal lymph node uptake following subcutaneous injection was found to correspond to a colloid particle size between 10 and 50 nm. Lymphoscintigraphy was found to be useful in the study of lymphatic drainage from the primary tumour site in patients with malignant melanoma on the trunk. Quantitative analysis of ilio-inguinal lymph node uptake in patients with malignant melanoma on the lower extremities was, however, found to be of no value for the detection of metastatic disease in lymph nodes. High absorbed doses may be received in lymph nodes (up to 1 mGy/MBq) and at the injection site (about 10 mGy/MBq). In an experimental study it was found that the relative colloid uptake in bone marrow and spleen depended on the total number of intravenously injected particles. This may considerably affect the absorbed dose in these organs. (author)

Cracking in Drying Colloidal Films

Science.gov (United States)

Singh, Karnail B.; Tirumkudulu, Mahesh S.

2007-05-01

It has long been known that thick films of colloidal dispersions such as wet clays, paints, and coatings crack under drying. Although capillary stresses generated during drying have been recently identified as the cause for cracking, the existence of a maximum crack-free film thickness that depends on particle size, rigidity, and packing has not been understood. Here, we identify two distinct regimes for crack-free films based on the magnitude of compressive strain at the maximum attainable capillary pressure and show remarkable agreement of measurements with our theory. We anticipate our results to not only form the basis for design of coating formulations for the paints, coatings, and ceramics industry but also assist in the production of crack-free photonic band gap crystals.

Redox active polymers and colloidal particles for flow batteries

Science.gov (United States)

Gavvalapalli, Nagarjuna; Moore, Jeffrey S.; Rodriguez-Lopez, Joaquin; Cheng, Kevin; Shen, Mei; Lichtenstein, Timothy

2018-05-29

The invention provides a redox flow battery comprising a microporous or nanoporous size-exclusion membrane, wherein one cell of the battery contains a redox-active polymer dissolved in the non-aqueous solvent or a redox-active colloidal particle dispersed in the non-aqueous solvent. The redox flow battery provides enhanced ionic conductivity across the electrolyte separator and reduced redox-active species crossover, thereby improving the performance and enabling widespread utilization. Redox active poly(vinylbenzyl ethylviologen) (RAPs) and redox active colloidal particles (RACs) were prepared and were found to be highly effective redox species. Controlled potential bulk electrolysis indicates that 94-99% of the nominal charge on different RAPs is accessible and the electrolysis products are stable upon cycling. The high concentration attainable (>2.0 M) for RAPs in common non-aqueous battery solvents, their electrochemical and chemical reversibility, and their hindered transport across porous separators make them attractive materials for non-aqueous redox flow batteries based on size-selectivity.

EFFECT OF HEAT-DISPERSING ON STICKIES AND THEIR REMOVAL IN POST-FLOTATION

OpenAIRE

Yang Gao,; Menghua Qin,; Hailong Yu,; Fengshan Zhang

2012-01-01

The effect of heat-dispersing on sticky substances in a deinking pulping line was studied under different conditions including varying temperature, disc clearance, and pulp consistency. Sticky substances were quantitatively investigated before and after the heat-dispersing, and categorized into macro-, mini-, and micro-stickies as well as dissolved and colloidal substances. Meanwhile, their extents of removal in post-flotation were evaluated. The results showed that raising temperature, reduc...

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

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

Colloid formation in groundwater by subsurface aeration: characterisation of the geo-colloids and their counterparts

International Nuclear Information System (INIS)

Wolthoorn, Anke; Temminghoff, Erwin J.M.; Riemsdijk, Willem H. van

2004-01-01

Subsurface aeration is used to oxidise Fe in situ in groundwater to make the water potable. In a groundwater system with pH > 7, subsurface aeration results in a non-mobile Fe precipitate and mobile Fe colloids. Since originally the goal of subsurface aeration is to remove Fe in situ, the formation of non-mobile Fe precipitate is the desired result. In addition to this intended effect, subsurface aeration may also strongly enhance the microbiological removal of NH 4 in the purification station. A hypothesis is that mobile Fe colloids may be the link between subsurface aeration and the positive effect on the microbiological removal of NH 4 . The objective of this study is to characterise the mobile Fe colloids and to derive a synthetic substitute for the naturally formed Fe colloids in order to be able to apply the Fe colloids as a management tool to enhance the removal of NH 4 in the process of producing drinking water from groundwater. At a purification station in The Netherlands natural Fe colloids from an aerated well were sampled. Furthermore, eight synthetic Fe colloids were prepared by oxidising synthetic solutions differing in elemental composition. The colloids were analysed using chemical analysis and electron microscopy (SEM and SEM-EDAX). The Fe colloids sampled in the field contained Fe, Ca, Na, PO 4 and Mn. Also in the synthetic Fe colloids PO 4 , Ca, Na and Mn were the most important elements next to Fe. Phosphate and dissolved organic C strongly influenced the morphology of the synthetic Fe colloids. When both the elemental composition and the morphology of the Fe colloids are taken into account, the synthetic Fe colloids formed in the synthetic solution containing Fe, Mn, PO 4 , SiO 4 and dissolved organic matter best match the Fe colloids from the field

Colloid formation in groundwater by subsurface aeration: characterisation of the geo-colloids and their counterparts

Energy Technology Data Exchange (ETDEWEB)

Wolthoorn, Anke; Temminghoff, Erwin J.M.; Riemsdijk, Willem H. van

2004-09-01

Subsurface aeration is used to oxidise Fe in situ in groundwater to make the water potable. In a groundwater system with pH > 7, subsurface aeration results in a non-mobile Fe precipitate and mobile Fe colloids. Since originally the goal of subsurface aeration is to remove Fe in situ, the formation of non-mobile Fe precipitate is the desired result. In addition to this intended effect, subsurface aeration may also strongly enhance the microbiological removal of NH{sub 4} in the purification station. A hypothesis is that mobile Fe colloids may be the link between subsurface aeration and the positive effect on the microbiological removal of NH{sub 4}. The objective of this study is to characterise the mobile Fe colloids and to derive a synthetic substitute for the naturally formed Fe colloids in order to be able to apply the Fe colloids as a management tool to enhance the removal of NH{sub 4} in the process of producing drinking water from groundwater. At a purification station in The Netherlands natural Fe colloids from an aerated well were sampled. Furthermore, eight synthetic Fe colloids were prepared by oxidising synthetic solutions differing in elemental composition. The colloids were analysed using chemical analysis and electron microscopy (SEM and SEM-EDAX). The Fe colloids sampled in the field contained Fe, Ca, Na, PO{sub 4} and Mn. Also in the synthetic Fe colloids PO{sub 4}, Ca, Na and Mn were the most important elements next to Fe. Phosphate and dissolved organic C strongly influenced the morphology of the synthetic Fe colloids. When both the elemental composition and the morphology of the Fe colloids are taken into account, the synthetic Fe colloids formed in the synthetic solution containing Fe, Mn, PO{sub 4}, SiO{sub 4} and dissolved organic matter best match the Fe colloids from the field.

Colloidal glasses

Indian Academy of Sciences (India)

First page Back Continue Last page Overview Graphics. Colloidal glasses. Glassy state is attained when system fails to reach equilibrium due to crowding of constituent particles. In molecular glasses, glassy state is reached by rapidly lowering the temperature. In colloidal glasses, glassy state is reached by increasing the ...

Preparation and characterization compatible pellets for immobilization of colloidal sulphur nanoparticles

Science.gov (United States)

Adlim, M.; Zarlaida, F.; Khaldun, I.; Dewi, R.; Jamilah, M.

2018-03-01

Mercury pollution in atmosphere is dominated by mercury vapour release from coal burning and gold-amalgam separation in gold mining. The initial steps in formulating a compatible mercury absorbent for mercury stabilization was fabrication of pellet supported colloidal sulphur. Sulphur is used to stabilize mercury vapour by formation of metacinnabar that has much lower toxicity. The sulphur reactivity toward mercury vapour can be enhanced by using colloidal sulphur nanoparticles immobilized on compatible pellets. Clay pellets would have heat resistance but in fact, they were less stable in aqueous solution although their stability increased with inclusion of rice husk ash and sawdust or pineapple leaf fibre in the composite. Pellets made of rice husk ash and polyvinyl acetate were stable in water at least for 24 hours. Sulphur from thiosulfate precursor that immobilized onto surface of pellet using chitosan as the stabilizer and the binding agent gave lower sulphur content compared to sulphur from other precursors (sulphur powder and sulphur-CS2). Sulphur from thiosulfate precursor was in form of colloid, has nanosize, and disperse particles on the surface of rice husk ash pellets. Sulphur immobilization methods affect on sulphur particles exposure on the pellet surface.

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

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.

Colloid formation during waste glass corrosion

International Nuclear Information System (INIS)

Mertz, C.J.; Buck, E.C.; Fortner, J.A.; Bates, J.K.

1996-01-01

The long-term behavior of nuclear waste glass in a geologic repository may require a technical consideration of the role of colloids in the release and transport of radionuclides. The neglect of colloidal properties in assessing the near- and far-field migration behavior of actinides may lead to significant underestimates and poor predictions of biosphere exposure from high-level waste (HLW) disposal. Existing data on colloid-facilitated transport suggests that radionuclide migration may be enhanced, but the importance of colloids is not adequately assessed. Indeed, the occurrence of radionuclide transport, attributed to colloidal species, has been reported at Mortandad Canyon, Los Alamos and at the Nevada Test Site; both unsaturated regions are similar to the proposed HLW repository at Yucca Mountain. Although some developments have been made on understanding the transport characteristics of colloids, the characterization of colloids generated from the corrosion of the waste form has been limited. Colloids are known to incorporate radionuclides either from hydrolysis of dissolved species (real colloids) or from adsorption of dissolved species onto existing groundwater colloids (pseudocolloids); however, these colloids may be considered secondary and solubility limited when compared to the colloids generated during glass alteration

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.)

Sustainable colloidal-silver-impregnated ceramic filter for point-of-use water treatment.

Science.gov (United States)

Oyanedel-Craver, Vinka A; Smith, James A

2008-02-01

Cylindrical colloidal-silver-impregnated ceramic filters for household (point-of-use) water treatment were manufactured and tested for performance in the laboratory with respect to flow rate and bacteria transport. Filters were manufactured by combining clay-rich soil with water, grog (previously fired clay), and flour, pressing them into cylinders, and firing them at 900 degrees C for 8 h. The pore-size distribution of the resulting ceramic filters was quantified by mercury porosimetry. Colloidal silver was applied to filters in different quantities and ways (dipping and painting). Filters were also tested without any colloidal-silver application. Hydraulic conductivity of the filters was quantified using changing-head permeability tests. [3H]H2O water was used as a conservative tracer to quantify advection velocities and the coefficient of hydrodynamic dispersion. Escherichia coli (E. coli) was used to quantify bacterial transport through the filters. Hydraulic conductivity and pore-size distribution varied with filter composition; hydraulic conductivities were on the order of 10(-5) cm/s and more than 50% of the pores for each filter had diameters ranging from 0.02 to 15 microm. The filters removed between 97.8% and 100% of the applied bacteria; colloidal-silver treatments improved filter performance, presumably by deactivation of bacteria. The quantity of colloidal silver applied per filter was more important to bacteria removal than the method of application. Silver concentrations in effluent filter water were initially greater than 0.1 mg/L, but dropped below this value after 200 min of continuous operation. These results indicate that colloidal-silver-impregnated ceramic filters, which can be made using primarily local materials and labor, show promise as an effective and sustainable point-of-use water treatment technology for the world's poorest communities.

UZ Colloid Transport Model

International Nuclear Information System (INIS)

McGraw, M.

2000-01-01

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

Programming Hierarchical Self-Assembly of Patchy Particles into Colloidal Crystals via Colloidal Molecules.

Science.gov (United States)

Morphew, Daniel; Shaw, James; Avins, Christopher; Chakrabarti, Dwaipayan

2018-03-27

Colloidal self-assembly is a promising bottom-up route to a wide variety of three-dimensional structures, from clusters to crystals. Programming hierarchical self-assembly of colloidal building blocks, which can give rise to structures ordered at multiple levels to rival biological complexity, poses a multiscale design problem. Here we explore a generic design principle that exploits a hierarchy of interaction strengths and employ this design principle in computer simulations to demonstrate the hierarchical self-assembly of triblock patchy colloidal particles into two distinct colloidal crystals. We obtain cubic diamond and body-centered cubic crystals via distinct clusters of uniform size and shape, namely, tetrahedra and octahedra, respectively. Such a conceptual design framework has the potential to reliably encode hierarchical self-assembly of colloidal particles into a high level of sophistication. Moreover, the design framework underpins a bottom-up route to cubic diamond colloidal crystals, which have remained elusive despite being much sought after for their attractive photonic applications.

Colloid migration in fractured media

International Nuclear Information System (INIS)

Hunt, J.R.

1989-01-01

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

Nanocomposites Based on Luminescent Colloidal Nanocrystals and Polymeric Ionic Liquids towards Optoelectronic Applications

Directory of Open Access Journals (Sweden)

Annamaria Panniello

2014-01-01

Full Text Available Polymeric ionic liquids (PILs are an interesting class of polyelectrolytes, merging peculiar physical-chemical features of ionic liquids with the flexibility, mechanical stability and processability typical of polymers. The combination of PILs with colloidal semiconducting nanocrystals leads to novel nanocomposite materials with high potential for batteries and solar cells. We report the synthesis and properties of a hybrid nanocomposite made of colloidal luminescent CdSe nanocrystals incorporated in a novel ex situ synthesized imidazolium-based PIL, namely, either a poly(N-vinyl-3-butylimidazolium hexafluorophosphate or a homologous PIL functionalized with a thiol end-group exhibiting a chemical affinity with the nanocrystal surface. A capping exchange procedure has been implemented for replacing the pristine organic capping molecules of the colloidal CdSe nanocrystals with inorganic chalcogenide ions, aiming to disperse the nano-objects in the PILs, by using a common polar solvent. The as-prepared nanocomposites have been studied by TEM investigation, UV-Vis, steady-state and time resolved photoluminescence spectroscopy for elucidating the effects of the PIL functionalization on the morphological and optical properties of the nanocomposites.

Colloid migration in groundwaters: Geochemical interactions of radionuclides with natural colloids. Final report

International Nuclear Information System (INIS)

Kim, J.J.; Longworth, G.; Hasler, S.E.; Gardiner, M.; Fritz, P.; Klotz, D.; Lazik, D.; Wolf, M.; Geyer, S.; Alexander, J.L.; Read, D.; Thomas, J.B.

1994-08-01

In this joint research programme the significance of groundwater colloids in far field radionuclide migration has been studied. The characterization, quantification and theoretical interpretation of colloid-borne transport phenomena for radionuclides were the main objectives of this research programme. Groundwaters, colloids and sediments were sampled from aquifer system overlying a saltdome in the Gorleben area in northern Germany and were characterized by various analytical methods (ICP-MS, ICP-AES, neutron activation analysis (NAA), DOC-Analyser, HPIC, potentiometric titration). Different natural isotopes ( 2 H, 3 H, 13 C, 14 C, 18 O, 34 S, U/Th decay series) were determined and their ratios were compared with one another in the order to ascertain the provenance of the groundwater colloids. The investigated groundwaters contain substantial amounts of colloids mainly composed of humic and fulvic acids loaded with various metal ions. The chemical interaction of radionuclide ions of various oxidation states (Am, Eu, for M(III), Th, Pu for M(IV), Np for M(V) and U for M(VI)) with groundwater colloids was investigated in order to elucidate the colloid facilitated migration behaviour of actinides in a given aquifer system. Transport process studies with generated pseudocolloids of radionuclides in various oxidation states were undertaken in scaled column experiments, pre-equilibrated with colloid rich Gorleben groundwater. A modelling programme was developed to predict chemical transport of radionuclides in the presence of humic colloids using a modified version of the CHEMTARD code. Modelling predictions have generated acceptable results for Eu, Am and U and poorer agreement between experimental and modelling results for Th and Np as a result of more limited data. (orig.)

Colloid migration in groundwaters: Geochemical interactions of radionuclides with natural colloids. Final report

Energy Technology Data Exchange (ETDEWEB)

Kim, J.J. [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Radiochemie; Delakowitz, B. [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Radiochemie; Zeh, P. [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Radiochemie; Probst, T. [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Radiochemie; Lin, X. [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Radiochemie; Ehrlicher, U. [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Radiochemie; Schauer, C. [Technische Univ. Muenchen, Garching (Germany). Inst. fuer Radiochemie; Ivanovich, M. [AEA Environment and Energy, Harwell (United Kingdom); Longworth, G. [AEA Environment and Energy, Harwell (United Kingdom); Hasler, S.E. [AEA Environment and Energy, Harwell (United Kingdom); Gardiner, M. [AEA Decommissioning and Radwaste, Harwell (United Kingdom); Fritz, P. [Gesellschaft fuer Strahlen- und Umweltforschung mbH Muenchen, Neuherberg (Germany); Klotz, D. [Gesellschaft fuer Strahlen- und Umweltforschung mbH Muenchen, Neuherberg (Germany); Lazik, D. [Gesellschaft fuer Strahlen- und Umweltforschung mbH Muenchen, Neuherberg (Germany); Wolf, M. [Gesellschaft fuer Strahlen- und Umweltforschung mbH Muenchen, Neuherberg (Germany); Geyer, S. [Gesellschaft fuer Strahlen- und Umweltforschung mbH Muenchen, Neuherberg (Germany); Alexander, J.L. [Atkins (W.S.) Engineering Sciences, Epsom (United Kingdom); Read, D. [Atkins (W.S.) Engineering Sciences, Epsom (United Kingdom); Thomas, J.B. [Atkins (W.S.) Engineering Sciences, Epsom (United Kingdom)

1994-08-01

In this joint research programme the significance of groundwater colloids in far field radionuclide migration has been studied. The characterization, quantification and theoretical interpretation of colloid-borne transport phenomena for radionuclides were the main objectives of this research programme. Groundwaters, colloids and sediments were sampled from aquifer system overlying a saltdome in the Gorleben area in northern Germany and were characterized by various analytical methods (ICP-MS, ICP-AES, neutron activation analysis (NAA), DOC-Analyser, HPIC, potentiometric titration). Different natural isotopes ({sup 2}H, {sup 3}H, {sup 13}C, {sup 14}C, {sup 18}O, {sup 34}S, U/Th decay series) were determined and their ratios were compared with one another in the order to ascertain the provenance of the groundwater colloids. The investigated groundwaters contain substantial amounts of colloids mainly composed of humic and fulvic acids loaded with various metal ions. The chemical interaction of radionuclide ions of various oxidation states (Am, Eu, for M(III), Th, Pu for M(IV), Np for M(V) and U for M(VI)) with groundwater colloids was investigated in order to elucidate the colloid facilitated migration behaviour of actinides in a given aquifer system. Transport process studies with generated pseudocolloids of radionuclides in various oxidation states were undertaken in scaled column experiments, pre-equilibrated with colloid rich Gorleben groundwater. A modelling programme was developed to predict chemical transport of radionuclides in the presence of humic colloids using a modified version of the CHEMTARD code. Modelling predictions have generated acceptable results for Eu, Am and U and poorer agreement between experimental and modelling results for Th and Np as a result of more limited data. (orig.)

[The study of antimicrobial properties of silver nanoparticles in the form of a colloidal solution in the matrix of finely dispersed silica].

Science.gov (United States)

Korchak, G I; Surmasheva, E V; Mikhienkova, A I; Nikonova, N A; Romanenko, L I; Oliĭnyk, Z A; Gorval', A K; Rosada, M A

2012-01-01

In the experimental study obtained with chemical method colloid solution of nanoparticles (NPs) of silver (Ag) and a composite on his base in the matrix of finely dispersed silica with particle size of 8-12 nm and NPs concentration in basic solution of 0,0016% (0,016 mg/cm3) were established to exhibit high antimicrobial activity against the test organisms: E. coli, P. aeruginosa, S. Aureus and C. Albicans, which depended on a set of factors. Antibacterial properties of tissue impregnated with Ag-NPs were studied. As stabilizing substances a mixture of surface-active substance sodium dodecyl sulfate and polymer polyvinylpyrrolidone was used Before the beginning of the study effective neutralizer was tailored. Times of preservation of antimicrobial activity of test samples have been established, and also their stability throughout long term of supervision (24 months) has been shown. Effect of organic pollution on antimicrobal activity of the samples has been studied. Based on obtained results the algorithm of the study of antimicrobial properties of nanopreparations has been elaborated.

Harnessing the advantages of hard and soft colloids by the use of core-shell particles as interfacial stabilizers

NARCIS (Netherlands)

Buchcic, C.; Tromp, R.H.; Meinders, M.B.J.; Cohen Stuart, M.A.

2017-01-01

The ability of colloidal particles to penetrate fluid interfaces is a crucial factor in the preparation of particle stabilized disperse systems such as foams and emulsions. For hard micron-sized particles the insertion into fluid interfaces requires substantial energy input, but soft particles

Colloids in Biotechnology

CERN Document Server

Fanun, Monzer

2010-01-01

Colloids have come a long way from when Thomas Graham coined the term colloid to describe 'pseudo solutions'. This book enables scientists to close the gap between extensive research and translation into commercial options in biomedicine and biotechnology. It covers biosurfactants and surface properties, phase behavior, and orientational change of surfactant mixtures with peptides at the interface. It also covers adsorption of polymers and biopolymers on the surface and interface, discusses colloidal nanoparticles and their use in biotechnology, and delves into bioadhesion and microencapsulati

Sign change in the net force in sphere-plate and sphere-sphere systems immersed in nonpolar critical fluid due to the interplay between the critical Casimir and dispersion van der Waals forces.

Science.gov (United States)

Valchev, Galin; Dantchev, Daniel

2017-08-01

We study systems in which both long-ranged van der Waals and critical Casimir interactions are present. The latter arise as an effective force between bodies when immersed in a near-critical medium, say a nonpolar one-component fluid or a binary liquid mixture. They are due to the fact that the presence of the bodies modifies the order parameter profile of the medium between them as well as the spectrum of its allowed fluctuations. We study the interplay between these forces, as well as the total force (TF) between a spherical colloid particle and a thick planar slab and between two spherical colloid particles. We do that using general scaling arguments and mean-field-type calculations utilizing the Derjaguin and the surface integration approaches. They both are based on data of the forces between two parallel slabs separated at a distance L from each other, confining the fluctuating fluid medium characterized by its temperature T and chemical potential μ. The surfaces of the colloid particles and the slab are coated by thin layers exerting strong preference to the liquid phase of the fluid, or one of the components of the mixture, modeled by strong adsorbing local surface potentials, ensuring the so-called (+,+) boundary conditions. On the other hand, the core region of the slab and the particles influence the fluid by long-ranged competing dispersion potentials. We demonstrate that for a suitable set of colloids-fluid, slab-fluid, and fluid-fluid coupling parameters, the competition between the effects due to the coatings and the core regions of the objects involved result, when one changes T, μ, or L, in sign change of the Casimir force (CF) and the TF acting between the colloid and the slab, as well as between the colloids. This can be used for governing the behavior of objects, say colloidal particles, at small distances, say in colloid suspensions for preventing flocculation. It can also provide a strategy for solving problems with handling, feeding

Sign change in the net force in sphere-plate and sphere-sphere systems immersed in nonpolar critical fluid due to the interplay between the critical Casimir and dispersion van der Waals forces

Science.gov (United States)

Valchev, Galin; Dantchev, Daniel

2017-08-01

We study systems in which both long-ranged van der Waals and critical Casimir interactions are present. The latter arise as an effective force between bodies when immersed in a near-critical medium, say a nonpolar one-component fluid or a binary liquid mixture. They are due to the fact that the presence of the bodies modifies the order parameter profile of the medium between them as well as the spectrum of its allowed fluctuations. We study the interplay between these forces, as well as the total force (TF) between a spherical colloid particle and a thick planar slab and between two spherical colloid particles. We do that using general scaling arguments and mean-field-type calculations utilizing the Derjaguin and the surface integration approaches. They both are based on data of the forces between two parallel slabs separated at a distance L from each other, confining the fluctuating fluid medium characterized by its temperature T and chemical potential μ . The surfaces of the colloid particles and the slab are coated by thin layers exerting strong preference to the liquid phase of the fluid, or one of the components of the mixture, modeled by strong adsorbing local surface potentials, ensuring the so-called (+,+) boundary conditions. On the other hand, the core region of the slab and the particles influence the fluid by long-ranged competing dispersion potentials. We demonstrate that for a suitable set of colloids-fluid, slab-fluid, and fluid-fluid coupling parameters, the competition between the effects due to the coatings and the core regions of the objects involved result, when one changes T , μ , or L , in sign change of the Casimir force (CF) and the TF acting between the colloid and the slab, as well as between the colloids. This can be used for governing the behavior of objects, say colloidal particles, at small distances, say in colloid suspensions for preventing flocculation. It can also provide a strategy for solving problems with handling, feeding

Cobalt ferrite nanoparticles with improved aqueous colloidal stability and electrophoretic mobility

International Nuclear Information System (INIS)

Munjal, Sandeep; Khare, Neeraj

2016-01-01

We have synthesized CoFe 2 O 4 (CFO) nanoparticles of size ∼ 12.2 nm by hydrothermal synthesis method. To control the size of these CFO nanoparticles, oleic acid was used as a surfactant. The inverse spinel phase of the synthesized nanoparticles was confirmed by X-ray diffraction method. As synthesized oleic acid coated CFO (OA@CFO) nanoparticles has very less electrophoretic mobility in the water and are not water dispersible. These OA@CFO nanoparticles were successfully turned into water soluble phase with a better colloidal aqueous stability, through a chemical treatment using citric acid. The modified citric acid coated CFO (CA@CFO) nanoparticles were dispersible in water and form a stable aqueous solution with high electrophoretic mobility.

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

A column experiment for the study of colloidal radionuclide migration in Gorleben aquifer systems

International Nuclear Information System (INIS)

Kim, J.I.; Delakowitz, B.; Zeh, P.; Klotz, D.; Lazik, D.

1994-01-01

A column experiment is performed for the assessment of the migration behaviour of trivalent 152 Eu, 241 Am and tetra- and pentavalent 237 Np, 233 Pa in the presence of humic colloids. Groundwater of an organic rich aquifer from the geological site at Gorleben is chosen for the experiment, as this has been well characterized during the earlier work and contains a substantial amount of humic colloids. The chemical and mineralogical composition of the pleistocene quartz-sand used in the column experiment is characterized by various analytical and mineralogical methods. Prior to the actinide migration experiment, the hydraulic properties (flow velocity, effective porosity, longitudinal dispersion coefficient) are determined in order to ascertain stable conditions for the experiment. In addition, the microstructure parameters (sediment surface, pore size distribution) of the groundwater-sand system in the column are determined. Radiotracers used for the determination of the hydraulic properties are 3 HHO and 82 Br - . Results obtained to date indicate a relatively high mobility of the lanthanide and actinide ions loaded on aquatic humic colloids. The recovery of injected radiotracer ions in eluates is found to depend on the flow velocity of groundwater through the column. The results help to elucidate the actinide migration behaviour in the presence of natural humic colloids. (orig.)

Experimental investigation on the use of highly charged nanoparticles to improve the stability of weakly charged colloidal system.

Science.gov (United States)

Zubir, Mohd Nashrul Mohd; Badarudin, A; Kazi, S N; Misran, Misni; Amiri, Ahmad; Sadri, Rad; Khalid, Solangi

2015-09-15

The present work highlighted on the implementation of a unique concept for stabilizing colloids at their incipiently low charge potential. A highly charged nanoparticle was introduced within a coagulated prone colloidal system, serving as stabilizer to resist otherwise rapid flocculation and sedimentation process. A low size asymmetry of nanoparticle/colloid serves as the new topic of investigation in addition to the well-established large size ratio nanoparticle/microparticle study. Highly charged Al2O3 nanoparticles were used within the present research context to stabilize TiO2 and Fe3O4 based colloids via the formation of composite structures. It was believed, based on the experimental evidence, that Al2O3 nanoparticle interact with the weakly charged TiO2 and Fe3O4 colloids within the binary system via absorption and/or haloing modes to increase the overall charge potential of the respective colloids, thus preventing further surface contact via van der Waal's attraction. Series of experimental results strongly suggest the presence of weakly charged colloids in the studied bimodal system where, in the absence of highly charged nanoparticle, experience rapid instability. Absorbance measurement indicated that the colloidal stability drops in accordance to the highly charged nanoparticle sedimentation rate, suggesting the dominant influence of nanoparticles to attain a well-dispersed binary system. Further, it was found that the level of colloidal stability was enhanced with increasing nanoparticle fraction within the mixture. Rheological observation revealed that each hybrid complexes demonstrated behavior reminiscence to water with negligible increase in viscosity which serves as highly favorable condition particularly in thermal transport applications. Copyright © 2015 Elsevier Inc. All rights reserved.

Stability enhancement of an electrically tunable colloidal photonic crystal using modified electrodes with a large electrochemical potential window

Energy Technology Data Exchange (ETDEWEB)

Shim, HongShik [Samsung Advanced Institute of Technology, Yongin-Si, Gyeonggi-do (Korea, Republic of); Department of Chemistry, Seoul National University, Seoul (Korea, Republic of); Gyun Shin, Chang; Heo, Chul-Joon; Jeon, Seog-Jin; Jin, Haishun; Woo Kim, Jung; Jin, YongWan; Lee, SangYoon; Gyu Han, Moon, E-mail: moongyu.han@samsung.com, E-mail: jinklee@snu.ac.kr [Samsung Advanced Institute of Technology, Yongin-Si, Gyeonggi-do (Korea, Republic of); Lim, Joohyun; Lee, Jin-Kyu, E-mail: moongyu.han@samsung.com, E-mail: jinklee@snu.ac.kr [Department of Chemistry, Seoul National University, Seoul (Korea, Republic of)

2014-02-03

The color tuning behavior and switching stability of an electrically tunable colloidal photonic crystal system were studied with particular focus on the electrochemical aspects. Photonic color tuning of the colloidal arrays composed of monodisperse particles dispersed in water was achieved using external electric field through lattice constant manipulation. However, the number of effective color tuning cycle was limited due to generation of unwanted ions by electrolysis of the water medium during electrical switching. By introducing larger electrochemical potential window electrodes, such as conductive diamond-like carbon or boron-doped diamond, the switching stability was appreciably enhanced through reducing the number of ions generated.

Colloidal polymer particles as catalyst carriers and phase transfer agents in multiphasic hydroformylation reactions.

Science.gov (United States)

Peral, D; Stehl, D; Bibouche, B; Yu, H; Mardoukh, J; Schomäcker, R; Klitzing, R von; Vogt, D

2018-03-01

Colloidal particles have been used to covalently bind ligands for the heterogenization of homogeneous catalysts. The replacement of the covalent bonds by electrostatic interactions between particles and the catalyst could preserve the selectivity of a truly homogeneous catalytic process. Functionalized polymer particles with trimethylammonium moieties, dispersed in water, with a hydrophobic core and a hydrophilic shell have been synthesized by emulsion polymerization and have been thoroughly characterized. The ability of the particles with different monomer compositions to act as catalyst carriers has been studied. Finally, the colloidal dispersions have been applied as phase transfer agents in the multiphasic rhodium-catalyzed hydroformylation of 1-octene. The hydrodynamic radius of the particles has been shown to be around 100 nm, and a core-shell structure could be observed by atomic force microscopy. The polymer particles were proven to act as carriers for the water-soluble hydroformylation catalyst, due to electrostatic interaction between the functionalized particles bearing ammonium groups and the sulfonated ligands of the catalyst. The particles were stable under the hydroformylation conditions and the aqueous catalyst phase could be recycled three times. Copyright © 2017 Elsevier Inc. All rights reserved.

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

Science.gov (United States)

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

2013-04-01

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

On adiabatic pair potentials of highly charged colloid particles

Science.gov (United States)

Sogami, Ikuo S.

2018-03-01

Generalizing the Debye-Hückel formalism, we develop a new mean field theory for adiabatic pair potentials of highly charged particles in colloid dispersions. The unoccupied volume and the osmotic pressure are the key concepts to describe the chemical and thermodynamical equilibrium of the gas of small ions in the outside region of all of the colloid particles. To define the proper thermodynamic quantities, it is postulated to take an ensemble averaging with respect to the particle configurations in the integrals for their densities consisting of the electric potential satisfying a set of equations that are derived by linearizing the Poisson-Boltzmann equation. With the Fourier integral representation of the electric potential, we calculate first the internal electric energy of the system from which the Helmholtz free energy is obtained through the Legendre transformation. Then, the Gibbs free energy is calculated using both ways of the Legendre transformation with respect to the unoccupied volume and the summation of chemical potentials. The thermodynamic functions provide three types of pair potentials, all of which are inversely proportional to the fraction of the unoccupied volume. At the limit when the fraction factor reduces to unity, the Helmholtz pair potential turns exactly into the well known Derjaguin-Landau-Verwey-Overbeek repulsive potential. The Gibbs pair potential possessing a medium-range strong repulsive part and a long-range weak attractive tail can explain the Schulze-Hardy rule for coagulation in combination with the van der Waals-London potential and describes a rich variety of phenomena of phase transitions observed in the dilute dispersions of highly charged particles.

Colloidal characterization of ultrafine silicon carbide and silicon nitride powders

Science.gov (United States)

Whitman, Pamela K.; Feke, Donald L.

1986-01-01

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

Semiconductor nanocrystals dispersed in imidazolium-based ionic liquids: a spectroscopic and morphological investigation

International Nuclear Information System (INIS)

Panniello, Annamaria; Binetti, Enrico; Ingrosso, Chiara; Curri, M. Lucia; Agostiano, Angela; Tommasi, Raffaele; Striccoli, Marinella

2013-01-01

A growing interest is devoted to the study of imidazolium-based ionic liquids as innovative materials to combine with functional elements for advanced technological applications. Materials based on semiconductor and oxide nanocrystals in ionic liquids can be promising for their integration in lithium batteries, as well as in innovative solar cells. Although the physical chemical properties and the solvation dynamics of bare ionic liquids have been extensively studied, their combination with colloidal nanocrystals still remains almost unexplored. Here, the optical properties of organic-capped luminescent cadmium selenide nanocrystals coated by a shell of zinc sulfide (CdSe(ZnS)) dispersed in 1,3-dialkyl imidazolium ionic liquids have been investigated, also in dependence of the alkyl chain length on the imidazolium ring and of the anion nature, by using both time-integrated and time-resolved optical spectroscopy. The observed variations in decay profiles of the ionic liquid in presence of colloidal nanocrystals suggest that the dispersion of the nanostructures induces modifications in the ionic liquid structural order. Finally, atomic force microscopy analysis has provided insight into the topography of the investigated dispersions deposited as film, confirming the organization of the ionic liquids in super-structures, also upon nanocrystal incorporation.

Colloidal paradigm in supercapattery electrode systems

Science.gov (United States)

Chen, Kunfeng; Xue, Dongfeng

2018-01-01

Among decades of development, electrochemical energy storage systems are now sorely in need of a new design paradigm at the nano size and ion level to satisfy the higher energy and power demands. In this review paper, we introduce a new colloidal electrode paradigm for supercapattery that integrates multiple-scale forms of matter, i.e. ion clusters, colloidal ions, and nanosized materials, into one colloid system, coupled with multiple interactions, i.e. electrostatic, van der Waals forces, and chemical bonding, thus leading to the formation of many redox reactive centers. This colloidal electrode not only keeps the original ionic nature in colloidal materials, but also creates a new attribute of high electroactivity. Colloidal supercapattery is a perfect application example of the novel colloidal electrode, leading to higher specific capacitance than traditional electrode materials. The high electroactivity of the colloidal electrode mainly comes from the contribution of exposed reactive centers, owing to the confinement effect of carbon and a binder matrix. Systematic and thorough research on the colloidal system will significantly promote the development of fundamental science and the progress of advanced energy storage technology.

Liquid crystal colloids

CERN Document Server

Muševič, Igor

2017-01-01

This book brings together the many concepts and discoveries in liquid crystal colloids contributed over the last twenty years and scattered across numerous articles and book chapters. It provides both a historical overview of the development of the field and a clear perspective on the future applications in photonics. The book covers all phenomena observed in liquid crystal colloids with an emphasis on experimental tools and applications of topology in condensed matter, as well as practical micro-photonics applications. It includes a number of spectacular manifestations of new topological phenomena not found or difficult to observe in other systems. Starting from the early works on nematic colloids, it explains the basics of topological defects in ordered media, charge and winding, and the elastic forces between colloidal particles in nematics. Following a detailed description of experimental methods, such as optical tweezing and particle tracking, the book eases the reader into the theoretical part, which de...

Liquid Crystal Colloids

Science.gov (United States)

Smalyukh, Ivan I.

2018-03-01

Colloids are abundant in nature, science, and technology, with examples ranging from milk to quantum dots and the colloidal atom paradigm. Similarly, liquid crystal ordering is important in contexts ranging from biological membranes to laboratory models of cosmic strings and liquid crystal displays in consumer devices. Some of the most exciting recent developments in both of these soft matter fields emerge at their interface, in the fast-growing research arena of liquid crystal colloids. Mesoscale self-assembly in such systems may lead to artificial materials and to structures with emergent physical behavior arising from patterning of molecular order and nano- or microparticles into precisely controlled configurations. Liquid crystal colloids show exceptional promise for new discovery that may impinge on composite material fabrication, low-dimensional topology, photonics, and so on. Starting from physical underpinnings, I review the state of the art in this fast-growing field, with a focus on its scientific and technological potential.

The mechanism of hydrophilic and hydrophobic colloidal silicon dioxide types as glidants

OpenAIRE

Jonat, Stéphane

2005-01-01

AEROSIL® 200 is a hydrophilic highly disperse colloidal silicon dioxide (CSD) that is commonly used to improve flowability. This conventional CSD has low bulk and tapped densities and can produce dust if handled improperly. In order to improve its handling, special mechanical processes were developed for the homogeneous compaction of CSD. As a result, two new products have been recently introduced: AEROSIL® 200 VV and AEROSIL® R 972 V. AEROSIL® 200 VV is hydrophilic and chemically identical t...

Insulin-egg yolk dispersions in self microemulsifying system.

Science.gov (United States)

Singnurkar, P S; Gidwani, S K

2008-11-01

Formulation of insulin into a microemulsion very often presents a physicochemical instability during their preparation and storage. In order to overcome this lack of stability and facilitate the handling of these colloidal systems, stabilization of insulin in presence of hydrophobic components of a microemulsion appears as the most promising strategy. The present paper reports the use of egg yolk for stabilization of insulin in self microemulsifying dispersions. Insulin loaded egg yolk self microemulsifying dispersions were prepared by lyophilization followed by dispersion into self microemulsifying vehicle. The physicochemical characterization of selfmicroemulsifying dispersions includes such as insulin encapsulation efficiency, in vitro stability of insulin in presence of proteolytic enzymes and in vitro release. The biological activity of insulin from the dispersion was estimated by enzyme-linked immunosorbant assay and in vivo using Wistar diabetic rats. The particle size ranged 1.023±0.316 μm in diameter and insulin encapsulation efficiency was 98.2±0.9 %. Insulin hydrophobic self microemulsifying dispersions suppressed insulin release in pH 7.4 phosphate buffer and shown to protect insulin from enzymatic degradation in vitro in presence of chymotripsin. Egg yolk encapsulated insulin was bioactive, demonstrated through both in vivo and in vitro.

Driving dynamic colloidal assembly using eccentric self-propelled colloids

OpenAIRE

Ma, Zhan; Lei, Qun-li; Ni, Ran

2017-01-01

Designing protocols to dynamically direct the self-assembly of colloidal particles has become an important direction in soft matter physics because of the promising applications in fabrication of dynamic responsive functional materials. Here using computer simulations, we found that in the mixture of passive colloids and eccentric self-propelled active particles, when the eccentricity and self-propulsion of active particles are high enough, the eccentric active particles can push passive coll...

Crystallization of DNA-coated colloids

Science.gov (United States)

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

2015-01-01

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

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.

Size determinations of colloidal fat emulsions

DEFF Research Database (Denmark)

Kuntsche, Judith; Klaus, Katrin; Steiniger, Frank

2009-01-01

Size and size distributions of colloidal dispersions are of crucial importance for their performance and safety. In the present study, commercially available fat emulsions (Lipofundin N, Lipofundin MCT and Lipidem) were analyzed by photon correlation spectroscopy, laser diffraction with adequate...... was checked with mixtures of monodisperse polystyrene nanospheres. In addition, the ultrastructure of Lipofundin N and Lipofundin MCT was investigated by cryo-electron microscopy. All different particle sizing methods gave different mean sizes and size distributions but overall, results were in reasonable...... agreement. By all methods, a larger mean droplet size (between 350 and 400 nm) as well as a broader distribution was measured for Lipofundin N compared to Lipofundin MCT and Lipidem (mean droplet size between about 280 and 320 nm). Size distributions of Lipofundin MCT and Lipidem were very similar...

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)

Surfactant-enhanced flushing enhances colloid transport and alters macroporosity in diesel-contaminated soil.

Science.gov (United States)

Guan, Zhuo; Tang, Xiang-Yu; Nishimura, Taku; Katou, Hidetaka; Liu, Hui-Yun; Qing, Jing

2018-02-01

Soil contamination by diesel has been often reported as a result of accidental spillage, leakage and inappropriate use. Surfactant-enhanced soil flushing is a common remediation technique for soils contaminated by hydrophobic organic chemicals. In this study, soil flushing with linear alkylbenzene sulfonates (LAS, an anionic surfactant) was conducted for intact columns (15cm in diameter and 12cm in length) of diesel-contaminated farmland purple soil aged for one year in the field. Dynamics of colloid concentration in column outflow during flushing, diesel removal rate and resulting soil macroporosity change by flushing were analyzed. Removal rate of n-alkanes (representing the diesel) varied with the depth of the topsoil in the range of 14%-96% while the n-alkanes present at low concentrations in the subsoil were completely removed by LAS-enhanced flushing. Much higher colloid concentrations and larger colloid sizes were observed during LAS flushing in column outflow compared to water flushing. The X-ray micro-computed tomography analysis of flushed and unflushed soil cores showed that the proportion of fine macropores (30-250μm in diameter) was reduced significantly by LAS flushing treatment. This phenomenon can be attributed to enhanced clogging of fine macropores by colloids which exhibited higher concentration due to better dispersion by LAS. It can be inferred from this study that the application of LAS-enhanced flushing technique in the purple soil region should be cautious regarding the possibility of rapid colloid-associated contaminant transport via preferential pathways in the subsurface and the clogging of water-conducting soil pores. Copyright © 2017. Published by Elsevier B.V.

A short textbook of colloid chemistry

CERN Document Server

Jirgensons, B

1962-01-01

A Short Textbook of Colloid Chemistry, Second Revised Edition details the factual aspect of colloid chemistry that includes the basic facts, established empirical and mathematical relationships, and practical applications. The chapters of the title are organized into two parts. In the first part, the text discusses the general concepts of colloid chemistry, such as the history and scope, basic terms, and basic methods in experiment with colloids. Part Two covers the technical aspect of colloid chemistry, such as the optical properties, electrical properties, and viscosity. The book will be of

Insulin-egg yolk dispersions in self microemulsifying system

OpenAIRE

Singnurkar P; Gidwani S

2008-01-01

Formulation of insulin into a microemulsion very often presents a physicochemical instability during their preparation and storage. In order to overcome this lack of stability and facilitate the handling of these colloidal systems, stabilization of insulin in presence of hydrophobic components of a microemulsion appears as the most promising strategy. The present paper reports the use of egg yolk for stabilization of insulin in self microemulsifying dispersions. Insulin loaded egg yolk self m...

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

Hemocompatibility of ultrafine systems on the basis of chitosan and its derivatives polymer-colloid complexes

Directory of Open Access Journals (Sweden)

M.V. Bazunova

2015-03-01

Full Text Available This article presents the results of the development process for the preparation of micro and nano-sized polymer-colloid com-plexes (РСС on the basis of water-soluble natural polymer chitosan (СTZ and the sodium salt of chitosan succinylamid (SСTZ with silver halide sols in aqueous media. Results of research of СTZ, sodium salt of SСTZ solutions and PСС of CTZ and SСTZ with colloidal parti-cles of silver iodide influence on structurally-functional properties of erythrocytes’ membranes on model of acidic hemolisis are presented in the article. Their influence on the nature of erythrocytes distribution by degree of their stability and on kinetic parameters (the beginning, intensity and completion of process of their destruction under the influence of the damaging agent (HCl is shown. The comparative analysis of results convinces that СTZ, SСTZ solutions and disperse systems on the basis of PСС of СTZ and SСTZ with colloidal particles of the silver iodide are capable of modulating variously matrix properties of erythrocytes of blood.

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

Control of colloids with gravity, temperature gradients, and electric fields

CERN Document Server

Sullivan, M; Harrison, C; Austin, R H; Megens, M; Hollingsworth, A; Russel, W B; Cheng Zhen; Mason, T; Chaikin, P M

2003-01-01

We have used a variety of different applied fields to control the density, growth, and structure of colloidal crystals. Gravity exerts a body force proportional to the buoyant mass and in equilibrium produces a height-dependent concentration profile. A similar body force can be obtained with electric fields on charged particles (electrophoresis), a temperature gradient on all particles, or an electric field gradient on uncharged particles (dielectrophoresis). The last is particularly interesting since its magnitude and sign can be changed by tuning the applied frequency. We study these effects in bulk (making 'dielectrophoretic bottles' or traps), to control concentration profiles during nucleation and growth and near surfaces. We also study control of non-spherical and optically anisotropic particles with the light field from laser tweezers.

Control of colloids with gravity, temperature gradients, and electric fields

Energy Technology Data Exchange (ETDEWEB)

Sullivan, Matt [Department of Physics, Princeton University, Princeton, NJ (United States); Zhao Kun [Department of Physics, Princeton University, Princeton, NJ (United States); Harrison, Christopher [Department of Physics, Princeton University, Princeton, NJ (United States); Austin, Robert H [Department of Physics, Princeton University, Princeton, NJ (United States); Megens, Mischa [Department of Physics, Princeton University, Princeton, NJ (United States); Hollingsworth, Andrew [Department of Chemical Engineering, Princeton University, Princeton, NJ (United States); Russel, William B [Department of Chemical Engineering, Princeton University, Princeton, NJ (United States); Cheng Zhengdong [ExxonMobil Research, Annandale, NJ (United States); Mason, Thomas [ExxonMobil Research, Annandale, NJ (United States); Chaikin, P M [Department of Physics, Princeton University, Princeton, NJ (United States)

2003-01-15

We have used a variety of different applied fields to control the density, growth, and structure of colloidal crystals. Gravity exerts a body force proportional to the buoyant mass and in equilibrium produces a height-dependent concentration profile. A similar body force can be obtained with electric fields on charged particles (electrophoresis), a temperature gradient on all particles, or an electric field gradient on uncharged particles (dielectrophoresis). The last is particularly interesting since its magnitude and sign can be changed by tuning the applied frequency. We study these effects in bulk (making 'dielectrophoretic bottles' or traps), to control concentration profiles during nucleation and growth and near surfaces. We also study control of non-spherical and optically anisotropic particles with the light field from laser tweezers.

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.

Design of Magnetic Gelatine/Silica Nanocomposites by Nanoemulsification: Encapsulation versus in Situ Growth of Iron Oxide Colloids

Directory of Open Access Journals (Sweden)

Joachim Allouche

2014-07-01

Full Text Available The design of magnetic nanoparticles by incorporation of iron oxide colloids within gelatine/silica hybrid nanoparticles has been performed for the first time through a nanoemulsion route using the encapsulation of pre-formed magnetite nanocrystals and the in situ precipitation of ferrous/ferric ions. The first method leads to bi-continuous hybrid nanocomposites containing a limited amount of well-dispersed magnetite colloids. In contrast, the second approach allows the formation of gelatine-silica core-shell nanostructures incorporating larger amounts of agglomerated iron oxide colloids. Both magnetic nanocomposites exhibit similar superparamagnetic behaviors. Whereas nanocomposites obtained via an in situ approach show a strong tendency to aggregate in solution, the encapsulation route allows further surface modification of the magnetic nanocomposites, leading to quaternary gold/iron oxide/silica/gelatine nanoparticles. Hence, such a first-time rational combination of nano-emulsion, nanocrystallization and sol-gel chemistry allows the elaboration of multi-component functional nanomaterials. This constitutes a step forward in the design of more complex bio-nanoplatforms.

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

Impact of in situ polymer coating on particle dispersion into solid laser-generated nanocomposites.

Science.gov (United States)

Wagener, Philipp; Brandes, Gudrun; Schwenke, Andreas; Barcikowski, Stephan

2011-03-21

The crucial step in the production of solid nanocomposites is the uniform embedding of nanoparticles into the polymer matrix, since the colloidal properties or specific physical properties are very sensitive to particle dispersion within the nanocomposite. Therefore, we studied a laser-based generation method of a nanocomposite which enables us to control the agglomeration of nanoparticles and to increase the single particle dispersion within polyurethane. For this purpose, we ablated targets of silver and copper inside a polymer-doped solution of tetrahydrofuran by a picosecond laser (using a pulse energy of 125 μJ at 33.3 kHz repetition rate) and hardened the resulting colloids into solid polymers. Electron microscopy of these nanocomposites revealed that primary particle size, agglomerate size and particle dispersion strongly depend on concentration of the polyurethane added before laser ablation. 0.3 wt% polyurethane is the optimal polymer concentration to produce nanocomposites with improved particle dispersion and adequate productivity. Lower polyurethane concentration results in agglomeration whereas higher concentration reduces the production rate significantly. The following evaporation step did not change the distribution of the nanocomposite inside the polyurethane matrix. Hence, the in situ coating of nanoparticles with polyurethane during laser ablation enables simple integration into the structural analogue polymer matrix without additives. Furthermore, it was possible to injection mold these in situ-stabilized nanocomposites without affecting particle dispersion. This clarifies that sufficient in situ stabilization during laser ablation in polymer solution is able to prevent agglomeration even in a hot polymer melt.

Clusters in attractive colloids

Energy Technology Data Exchange (ETDEWEB)

Coniglio, A [Dipartimento di Scienze Fisiche, Universita di Napoli ' Federico II' , Complesso Universitario di Monte Sant' Angelo, via Cintia 80126 Naples (Italy); Arcangelis, L de [Dipartimento di Ingegneria dell' Informazione and CNISM II Universita di Napoli, Aversa (CE) (Italy); Candia, A de [Dipartimento di Scienze Fisiche, Universita di Napoli ' Federico II' , Complesso Universitario di Monte Sant' Angelo, via Cintia 80126 Naples (Italy); Gado, E Del [Dipartimento di Scienze Fisiche, Universita di Napoli ' Federico II' , Complesso Universitario di Monte Sant' Angelo, via Cintia 80126 Naples (Italy); Fierro, A [Dipartimento di Scienze Fisiche, Universita di Napoli ' Federico II' , Complesso Universitario di Monte Sant' Angelo, via Cintia 80126 Naples (Italy); Sator, N [Laboratoire de Physique Theorique de la Matiere Condensee, Universite Pierre et Marie Curie-Paris6, UMR (CNRS) 7600 Case 121, 4 Place Jussieu 75252 Paris Cedex 05 (France)

2006-09-13

We discuss how the anomalous increase of the viscosity in colloidal systems with short-range attraction can be related to the formation of long-living clusters. Based on molecular dynamics and Monte Carlo numerical simulations of different models, we propose a similar picture for colloidal gelation at low and intermediate volume fractions. On this basis, we analyze the distinct role played by the formation of long-living bonds and the crowding of the particles in the slow dynamics of attractive colloidal systems.

Grimsel colloid exercise, an international intercomparison exercise on the sampling and characterization of groundwater colloids

International Nuclear Information System (INIS)

Degueldre, C.

1990-01-01

The Grimsel colloid exercise was an intercomparison exercise which consisted of an in situ sampling phase followed by a colloid characterization step. The goal of this benchmark exercise, which involved 12 laboratories, was to evaluate both sampling and characterization techniques with emphasis on the colloid specific size distribution. The sampling phase took place at the Grimsel test site between 1 and 13 February 1988 and the participating groups produced colloid samples using various methods. This work was carried out within the Community COCO Club, as a component of the Mirage project (second phase)

Colloidal agglomerates in tank sludge: Impact on waste processing. 1997 annual progress report

Energy Technology Data Exchange (ETDEWEB)

Virden, J.W.

1997-06-01

'Disposal of millions of gallons of existing radioactive wastes is a major remediation problem for the Department of Energy (DOE). Although radionuclides are the most hazardous waste con- stituents. the components of greatest concern from a waste processing standpoint are insoluble sludges consisting of submicron colloidal particles. Depending on processing conditions, these colloidal particles can form agglomerate networks that could clog transfer lines or interfere with solid-liquid separations such as settle-decant operations. Under different conditions, the particles can be dispersed to form very fine suspended particles that will not create sediment in settle- decant steps and that can foul and contaminate downstream treatment components including ion exchangers or filtrations systems. Given the wide range of tank chemistries present at Hanford and other DOE sites, it is impractical to measure the properties of all potential processing conditions to design effective treatment procedures. Instead. a framework needs to be established to allow sludge property trends to be predicted on a sound scientific basis. The scientific principles of greatest utility in characterizing, understanding, and controlling the physical properties of sludge fall in the realm of colloid chemistry. The objectives of this work are to accomplish the following: understand the factors controlling the nature and extent of colloidal agglomeration under expected waste processing conditions determine how agglomeration phenomena influence physical properties relevant to waste processing including rheology, sedimentation. and filtration develop strategies for optimizing processing conditions via control of agglomeration phenomena.'

Colloidal agglomerates in tank sludge: Impact on waste processing. 1997 annual progress report

International Nuclear Information System (INIS)

Virden, J.W.

1997-01-01

'Disposal of millions of gallons of existing radioactive wastes is a major remediation problem for the Department of Energy (DOE). Although radionuclides are the most hazardous waste constituents. the components of greatest concern from a waste processing standpoint are insoluble sludges consisting of submicron colloidal particles. Depending on processing conditions, these colloidal particles can form agglomerate networks that could clog transfer lines or interfere with solid-liquid separations such as settle-decant operations. Under different conditions, the particles can be dispersed to form very fine suspended particles that will not create sediment in settle- decant steps and that can foul and contaminate downstream treatment components including ion exchangers or filtrations systems. Given the wide range of tank chemistries present at Hanford and other DOE sites, it is impractical to measure the properties of all potential processing conditions to design effective treatment procedures. Instead. a framework needs to be established to allow sludge property trends to be predicted on a sound scientific basis. The scientific principles of greatest utility in characterizing, understanding, and controlling the physical properties of sludge fall in the realm of colloid chemistry. The objectives of this work are to accomplish the following: understand the factors controlling the nature and extent of colloidal agglomeration under expected waste processing conditions determine how agglomeration phenomena influence physical properties relevant to waste processing including rheology, sedimentation. and filtration develop strategies for optimizing processing conditions via control of agglomeration phenomena.'

Titanium in UK rural, agricultural and urban/industrial rivers: Geogenic and anthropogenic colloidal/sub-colloidal sources and the significance of within-river retention

Energy Technology Data Exchange (ETDEWEB)

Neal, Colin; Jarvie, Helen [Centre for Ecology and Hydrology, Wallingford, Crowmarsh Gifford, Wallingford, OXON, OX10 8BB (United Kingdom); Rowland, Philip, E-mail: apr@ceh.ac.uk [Centre for Ecology and Hydrology, Lancaster, Lancaster Environment Centre, Library Avenue, Bailrigg, Lancaster, LA1 4AP (United Kingdom); Lawler, Alan; Sleep, Darren; Scholefield, Paul [Centre for Ecology and Hydrology, Lancaster, Lancaster Environment Centre, Library Avenue, Bailrigg, Lancaster, LA1 4AP (United Kingdom)

2011-04-15

Operationally defined dissolved Titanium [Ti] (the < 0.45 {mu}m filtered fraction) in rivers draining rural, agricultural, urban and industrial land-use types in the UK averaged 2.1 {mu}g/l with a range in average of 0.55 to 6.48 {mu}g/l. The lowest averages occurred for the upland areas of mid-Wales the highest just downstream of major sewage treatment works (STWs). [Ti] in rainfall and cloud water in mid-Wales averaged 0.2 and 0.7 {mu}g/l, respectively. Average, baseflow and stormflow [Ti] were compared with two markers of sewage effluent and thus human population: soluble reactive phosphorus (SRP) and boron (B). While B reflects chemically conservative mixing, SRP declined downstream of STW inputs due to in-stream physico-chemical and biological uptake. The results are related to colloidal and sub-colloidal Ti inputs from urban/industrial conurbations coupled with diffuse background (geological) sources and within-river removal/retention under low flows as a result of processes of aggregation and sedimentation. The urban/industrial inputs increased background [Ti] by up to eleven fold, but the total anthropogenic Ti input might well have been underestimated owing to within-river retention. A baseline survey using cross-flow ultrafiltration revealed that up to 79% of the [Ti] was colloidal/nanoparticulate (> 1 kDa i.e. > c. 1-2 nm) for the rural areas, but as low as 28% for the urban/industrial rivers. This raises fundamental issues of the pollutant inputs of Ti, with the possibility of significant complexation of Ti in the sewage effluents and subsequent breakdown within the rivers, as well as the physical dispersion of fine colloids down to the macro-molecular scale. Although not directly measured, the particulate Ti can make an important contribution to the net Ti flux. - Research Highlights: {yields} Filtered Ti in agricultural, urban and industrial UK rivers described. {yields} Highest concentrations occur just downstream of STWs. {yields} The urban

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

THE LIME PURIFICATION OF SUGAR –CONTAINING SOLUTION USING HIGH VISCOSITY COLLOIDAL SOLUTIONS

Directory of Open Access Journals (Sweden)

K. V.

2015-12-01

Full Text Available Aim of the work was to determine the efficiency of combined application of lime and high-viscous suspensions, containing the aluminium nanoparticles as a precursor in treatment of sugar-containing solutions. At the first stage the aluminium nanopowder, encapsulated into a salt matrix, was produced by the combined precipitation from a gas phase of metal and halogenide of alkali metal (NaCl. For the long-term stabilization of aluminum nanoparticles the method, developed by the authors, for dispersing these powders in the composition of polyethylene glycols was used, providing the colloidal solution of high viscosity (gel. At the second stage, as an object of investigation a juice of sugar beet, produced in the laboratory conditions by water extracting from the beet chips, was applied. In the produced juice the main characteristics of its quality were determined: the content of solids, sucrose, its purity was calculated (ratio of sucrose to solids content, in%. The content of protein and pectin components was also determined (as the main components of the colloidal fraction of the diffusion juice. Conventionally, as a basic reagent for the process of a lime pretreatment a lime milk of 1.18 g/cm3 density, prepared by liming the burned lime using hot water, was used. During the experiments the effectiveness of reagents, containing aluminum in nanoform, on the degree of removal of the colloidal dispersion substances in the process of juice purification in sugar beet production and improvement of its quality, is shown. However, the obtained results show that, depending on the method of producing, the additional reagents with aluminium nanoparticles have different effect on change of diffusion juice purity in the process of its treatment by the lime milk.

A close collaboration of chitosan with lipid colloidal carriers for drug delivery applications.

Science.gov (United States)

Bugnicourt, Loïc; Ladavière, Catherine

2017-06-28

Chitosan and lipid colloids have separately shown a growing interest in the field of drug delivery applications. Their success is mainly due to their interesting physicochemical behaviors, as well as their biological properties such as bioactivity and biocompatibility. While chitosan is a well-known cationic polysaccharide with the ability to strongly interact with drugs and biological matrices through mainly electrostatic interactions, lipid colloids are carriers particularly recognized for the drug vectorization. In recent years, the combination of both entities has been considered because it offers new systems which gather the advantages of each of them to efficiently deliver various types of bioactive species. The purpose of this review is to describe these associations between chemically-unmodified chitosan chains (solubilized or dispersed) and lipid colloids (as nanoparticles or organized in lipid layers), as well as their potential in the drug delivery area so far. Three assemblies have mainly been reported in the literature: i) lipid nanoparticles (solid lipid nanoparticles or nanostructured lipid carriers) coated with chitosan chains, ii) lipid vesicles covered with chitosan chains, and iii) chitosan chains structured in nanoparticles with a lipid coating. Their elaboration processes, their physicochemical characterization, and their biological studies are detailed and discussed herein. The different bioactive species (drugs and bio(macro)molecules) incorporated in these assemblies, their maximal incorporation efficiency, and their loading capacity are also presented. This review reveals the versatility of these assemblies. Depending on the organization of lipids (i.e., nanoparticles or vesicles) and the state of polymer chains (i.e., solubilized or dispersed under the form of nanoparticles), a large variety of drugs can be successfully incorporated, and various routes of administration can be considered. Copyright © 2017 Elsevier B.V. All rights reserved.

Characterization of silver colloids formed in LiBbO3 by Ag and O implantation at room and elevated temperatures

International Nuclear Information System (INIS)

Williams, E.K.; Ila, D.; Darwish, A.; Poker, D.B.; Sarkisov, S.S.; Curley, M.J.; Wang, J.-C.; Svetchnikov, V.L.; Zandbergen, H.W.

1999-01-01

To address the issue of dispersion of Ag colloids in LiNbO 3 at heat treatment temperatures of 400-500 deg. C, Ag and O were implanted at energies of 160 and 35 keV, respectively, at room temperature (Rt) and at 500 deg. C. Fluences were 4x10 16 and 8x10 16 /cm 2 and the order of the Ag and O implants was varied. Electron paramagnetic resonance spectra indicated that only O followed by Ag implantation of 500 deg. C produced silver oxide. Optical absorption spectrometry and RBS showed significant differences in the dispersion of the colloids with implant temperature and implant order. Implantation of Ag at 1.5 MeV to a fluence of 2x10 16 /cm 2 followed by heat treatment at 500 deg. C for 1 h produced nonlinear optical waveguides with a nonlinear index of the order of 10 -10 cm 2 /W at 532 nm

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

Effect of highly dispersed yttria addition on thermal stability of hydroxyapatite

International Nuclear Information System (INIS)

Parente, P.; Savoini, B.; Ferrari, B.; Monge, M.A.; Pareja, R.; Sanchez-Herencia, A.J.

2013-01-01

The capability of the colloidal method to produce yttria (Y 2 O 3 ) dispersed hydroxyapatite (HA) has been investigated as an alternative method to the conventional method of mechanical mixing and sintering for developing HA-based materials that could exhibit controllable and enhanced functional properties. A water based colloidal route to produce HA materials with highly dispersed Y 2 O 3 has been applied, and the effect of 10 wt.% Y 2 O 3 addition to HA investigated by thermal analysis, X-ray diffraction and Fourier transform infrared spectroscopy. These measurements evidence a remarkable effect of this Y 2 O 3 addition on decomposition mechanisms of synthetic HA. Results show that incorporation of Y 2 O 3 as dispersed second phase is beneficial because it hinders the decomposition mechanisms of HA into calcium phosphates. This retardation will allow the control of the sintering conditions for developing HA implants with improved properties. Besides, substitution of Ca 2+ with Y 3+ ions appears to promote the formation of OH − vacancies, which could improve the conductive properties of HA favorable to osseointegration. - Highlights: ► We reveal the influence of Y 2 O 3 on thermal stability of hydroxyapatite. ► Incorporation of Y 2 O 3 delays decomposition of hydroxyapatite to calcium phosphates. ► Addition of Y 2 O 3 enables sintering conditions more favorable to the densification.

Fabricating colloidal crystals and construction of ordered nanostructures

Directory of Open Access Journals (Sweden)

Sun Zhiqiang

2006-01-01

Full Text Available AbstractColloidal crystals of polymeric or inorganic microspheres are of extensive interest due to their potential applications in such as sensing, optics, photonic bandgap and surface patterning. The article highlights a set of approaches developed in our group, which are efficient to prepare colloidal crystals with ordered voids, patterned colloidal crystals on non-planar surfaces, heterogeneous colloidal crystals of different building blocks, colloidal crystals composed of non-spherical polyhedrons, and colloidal crystals of non-close-packed colloidal microspheres in particular. The use of these colloidal crystals as templates for different microstructures range from nanoscale to micron-scale is also summarized.

Constructing of DNA vectors with controlled nanosize and single dispersion by block copolymer coating gold nanoparticles as template assembly

Energy Technology Data Exchange (ETDEWEB)

Li, Junbo, E-mail: Lijunbo@haust.edu.cn [Henan University of Science and Technology, School of Chemical Engineering and Pharmaceutics (China); Wu, Wenlan [Henan University of Science and Technology, School of Medicine (China); Gao, Jiayu; Liang, Ju; Zhou, Huiyun; Liang, Lijuan [Henan University of Science and Technology, School of Chemical Engineering and Pharmaceutics (China)

2017-03-15

Synthesized vectors with nanoscale size and stable colloid dispersion are highly desirable for improving gene delivery efficiency. Here, a core-shell template particle was constructed with polyethylene glycol-b-poly1-(3-aminopropyl)-3-(2-methacryloyloxy propylimidazolium bromine) (PEG-b-PAMPImB) coating gold nanoparticles (PEG-b-PAMPImB-@-Au NPs) for loading DNA and delivering in vitro. Data from transmission electron microscopy (TEM) and dynamic light scattering (DLS) suggest that these nanoplexes, by forming an electrostatic complex with DNA at the inner PAMPImB shell, offer steric protection for the outer PEG corona leading to single dispersion and small size. Notably, higher colloid stability and lower cytotoxicity were achieved with these nanoplexes when compared with PAMPImB monolayer-coated gold nanoparticles (Au NPs). Confocal laser scanning microscopy and intracellular trafficking TEM further indicate that the nanoplexes can translocate across the cell membrane and partly enter the nucleus for high efficient expression. Thus, template assembly represents a promising approach to control the size and colloid stability of gene vectors and ensure safety and efficiency of DNA delivery.

Constructing of DNA vectors with controlled nanosize and single dispersion by block copolymer coating gold nanoparticles as template assembly

Science.gov (United States)

Li, Junbo; Wu, Wenlan; Gao, Jiayu; Liang, Ju; Zhou, Huiyun; Liang, Lijuan

2017-03-01

Synthesized vectors with nanoscale size and stable colloid dispersion are highly desirable for improving gene delivery efficiency. Here, a core-shell template particle was constructed with polyethylene glycol- b-poly1-(3-aminopropyl)-3-(2-methacryloyloxy propylimidazolium bromine) (PEG- b-PAMPImB) coating gold nanoparticles (PEG- b-PAMPImB-@-Au NPs) for loading DNA and delivering in vitro. Data from transmission electron microscopy (TEM) and dynamic light scattering (DLS) suggest that these nanoplexes, by forming an electrostatic complex with DNA at the inner PAMPImB shell, offer steric protection for the outer PEG corona leading to single dispersion and small size. Notably, higher colloid stability and lower cytotoxicity were achieved with these nanoplexes when compared with PAMPImB monolayer-coated gold nanoparticles (Au NPs). Confocal laser scanning microscopy and intracellular trafficking TEM further indicate that the nanoplexes can translocate across the cell membrane and partly enter the nucleus for high efficient expression. Thus, template assembly represents a promising approach to control the size and colloid stability of gene vectors and ensure safety and efficiency of DNA delivery.

Synthesis and green up-conversion fluorescence of colloidal La0.78Yb0.20Er0.02F3/SiO2 core/shell nanocrystals

International Nuclear Information System (INIS)

Wang Yan; Qin Weiping; Zhang Jisen; Cao Chunyan; Zhang Jishuang; Jin Ye; Zhu Peifen; Wei Guodong; Wang Guofeng; Wang Lili

2007-01-01

Water-soluble PVP-stabilized hexagonal-phase La 0.78 Yb 0.20 Er 0.02 F 3 nanocrystals (NCs) were synthesized by hydrothermal method. The NCs were coated with a very thin silica shell, and amino groups were introduced to the surface of silica shells by copolymerization of 3-aminopropyl(triethoxy)silane. The core/shell NCs can be dispersed in ethanol and water to form stable colloidal solution. The transmission electron microscopy (TEM), selected area electron diffraction (SAED), powder X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR) were used to characterize the core/shell materials. In addition, the green up-conversion fluorescence mechanism of La 0.78 Yb 0.20 Er 0.02 F 3 /SiO 2 NCs was studied with a 980-nm diode laser as excitation source. The water solubility, small core/shell particles size, and well colloidal stability mean the green up-conversion fluorescence NCs have potential applications in bioassay. - Graphical abstract: Colloidal La 0.78 Yb 0.20 Er 0.02 F 3 /SiO 2 Core/Shell nanocrystals (NCs) were synthesized and the free amino groups were introduced to the surface of silica shells by copolymerization 3-aminopropyl(triethoxy)silane. The NCs can be dispersed in ethanol and water to form stable colloidal solution. In addition, the NCs exhibit green up-conversion fluorescence under 980-nm excitation

Optical and structural properties of ensembles of colloidal Ag2S quantum dots in gelatin

International Nuclear Information System (INIS)

Ovchinnikov, O. V.; Smirnov, M. S.; Shapiro, B. I.; Shatskikh, T. S.; Perepelitsa, A. S.; Korolev, N. V.

2015-01-01

The size dependences of the absorption and luminescence spectra of ensembles of hydrophilic colloidal Ag 2 S quantum dots produced by the sol-gel method and dispersed in gelatin are analyzed. By X-ray diffraction analysis and transmission electron microscopy, the formation of core/shell nanoparticles is detected. The characteristic feature of the nanoparticles is the formation of crystalline cores, 1.5–2.0 nm in dimensions, and shells of gelatin and its complexes with the components of synthesis. The observed slight size dependence of the position of infrared photoluminescence bands (in the range 1000–1400 nm) in the ensembles of hydrophilic colloidal Ag 2 S quantum dots is explained within the context of the model of the radiative recombination of electrons localized at structural and impurity defects with free holes

Antimicrobial and antioxidant potentials of biosynthesized colloidal zinc oxide nanoparticles for a fortified cold cream formulation: A potent nanocosmeceutical application.

Science.gov (United States)

S, Sonia; H, Linda Jeeva Kumari; K, Ruckmani; M, Sivakumar

2017-10-01

Nanocosmeceuticals are promising applications of nanotechnology in personal care industries. Zinc oxide is an inorganic material that is non-toxic and skin compatible with self-cleansing and microbicidal properties. Herein, exploitation of colloidal zinc oxide nanoparticles (ZnONps) as potent biomaterial for a topical formulation of cosmetic and dermatological significance is employed. ZnONps were green synthesized using environmentally benign Adhatoda vasica leaf extract and characterized by UV-Vis absorption spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), dynamic light scattering (DLS), high-resolution transmission electron microscopy (HR-TEM) and energy-dispersive X-ray spectroscopy (EDX). The results reveal that the biosynthesized ZnONps exhibit an absorption peak at 352nm. XRD and HR-TEM analyses confirm the hexagonal wurtzite structure of ZnONps with particle size of about 10nm to 12nm. Elemental analysis by EDX confirms the presence of zinc and oxygen. Zeta potential of -24.6mV affirms the stability of nanoparticles. The antibacterial and antifungal activities of biosynthesized ZnONps exhibit mean zone of inhibition from 08.667±0.282 to 21.666±0.447 (mm) and 09.000±0.177 to 19.000±0.307 (mm) respectively, in a dose-dependent manner. The IC 50 value exerted from the antioxidant activity of ZnONps is found to be 139.27μgmL -1 . ZnONps infused cold cream formulation of microbicidal and antioxidant properties was further tested against clinical skin pathogens. The nano-based cold cream exhibited significant inhibitory action against Candida sp., which showed resistance against a commercial antifungal cream (2%). Therefore, this study demonstrates the exploitation of ZnONps as promising colloidal drug carriers in cosmeceuticals that can significantly alleviate human skin infections and oxidative stress induced cellular damage. Copyright © 2017 Elsevier B.V. All rights reserved.

Quantitative uptake of colloidal particles by cell cultures

Energy Technology Data Exchange (ETDEWEB)

Feliu, Neus [Department of Physics, Philipps University Marburg, Marburg (Germany); Department for Clinical Science, Intervention and Technology (CLINTEC),Karolinska Institutet, Stockholm (Sweden); Hühn, Jonas; Zyuzin, Mikhail V.; Ashraf, Sumaira; Valdeperez, Daniel; Masood, Atif [Department of Physics, Philipps University Marburg, Marburg (Germany); Said, Alaa Hassan [Department of Physics, Philipps University Marburg, Marburg (Germany); Physics Department, Faculty of Science, South Valley University (Egypt); Escudero, Alberto [Department of Physics, Philipps University Marburg, Marburg (Germany); Instituto de Ciencia de Materiales de Sevilla, CSIC — Universidad de Sevilla, Seville (Spain); Pelaz, Beatriz [Department of Physics, Philipps University Marburg, Marburg (Germany); Gonzalez, Elena [Department of Physics, Philipps University Marburg, Marburg (Germany); University of Vigo, Vigo (Spain); Duarte, Miguel A. Correa [University of Vigo, Vigo (Spain); Roy, Sathi [Department of Physics, Philipps University Marburg, Marburg (Germany); Chakraborty, Indranath [Department of Chemistry, University of Illinois at Urbana Champaign, Urbana, IL (United States); Lim, Mei L.; Sjöqvist, Sebastian [Department for Clinical Science, Intervention and Technology (CLINTEC),Karolinska Institutet, Stockholm (Sweden); Jungebluth, Philipp [Department of Thoracic Surgery, Thoraxklinik, Heidelberg University, Heidelberg (Germany); Parak, Wolfgang J., E-mail: wolfgang.parak@physik.uni-marburg.de [Department of Physics, Philipps University Marburg, Marburg (Germany); CIC biomaGUNE, San Sebastian (Spain)

2016-10-15

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

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

Efficient One-Pot Synthesis of Colloidal Zirconium Oxide Nanoparticles for High-Refractive-Index Nanocomposites.

Science.gov (United States)

Liu, Chao; Hajagos, Tibor Jacob; Chen, Dustin; Chen, Yi; Kishpaugh, David; Pei, Qibing

2016-02-01

Zirconium oxide nanoparticles are promising candidates for optical engineering, photocatalysis, and high-κ dielectrics. However, reported synthetic methods for the colloidal zirconium oxide nanoparticles use unstable alkoxide precursors and have various other drawbacks, limiting their wide application. Here, we report a facile one-pot method for the synthesis of colloidally stable zirconium oxide nanoparticles. Using a simple solution of zirconium trifluoroacetate in oleylamine, highly stable zirconium oxide nanoparticles have been synthesized with high yield, following a proposed amidization-assisted sol-gel mechanism. The nanoparticles can be readily dispersed in nonpolar solvents, forming a long-term stable transparent solution, which can be further used to fabricate high-refractive-index nanocomposites in both monolith and thin-film forms. In addition, the same method has also been extended to the synthesis of titanium oxide nanoparticles, demonstrating its general applicability to all group IVB metal oxide nanoparticles.

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

Science.gov (United States)

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

2013-04-30

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

Modeling Evaporation and Particle Assembly in Colloidal Droplets.

Science.gov (United States)

Zhao, Mingfei; Yong, Xin

2017-06-13

Evaporation-induced assembly of nanoparticles in a drying droplet is of great importance in many engineering applications, including printing, coating, and thin film processing. The investigation of particle dynamics in evaporating droplets can provide fundamental hydrodynamic insight for revealing the processing-structure relationship in the particle self-organization induced by solvent evaporation. We develop a free-energy-based multiphase lattice Boltzmann method coupled with Brownian dynamics to simulate evaporating colloidal droplets on solid substrates with specified wetting properties. The influence of interface-bound nanoparticles on the surface tension and evaporation of a flat liquid-vapor interface is first quantified. The results indicate that the particles at the interface reduce surface tension and enhance evaporation flux. For evaporating particle-covered droplets on substrates with different wetting properties, we characterize the increase of evaporate rate via measuring droplet volume. We find that droplet evaporation is determined by the number density and circumferential distribution of interfacial particles. We further correlate particle dynamics and assembly to the evaporation-induced convection in the bulk and on the surface of droplet. Finally, we observe distinct final deposits from evaporating colloidal droplets with bulk-dispersed and interface-bound particles. In addition, the deposit pattern is also influenced by the equilibrium contact angle of droplet.

Particle and surfactant interactions effected polar and dispersive components of interfacial energy in nanocolloids

Science.gov (United States)

Harikrishnan, A. R.; Das, Sarit K.; Agnihotri, Prabhat K.; Dhar, Purbarun

2017-08-01

We segregate and report experimentally for the first time the polar and dispersive interfacial energy components of complex nanocolloidal dispersions. In the present study, we introduce a novel inverse protocol for the classical Owens Wendt method to determine the constitutive polar and dispersive elements of surface tension in such multicomponent fluidic systems. The effect of nanoparticles alone and aqueous surfactants alone are studied independently to understand the role of the concentration of the dispersed phase in modulating the constitutive elements of surface energy in fluids. Surfactants are capable of altering the polar component, and the combined particle and surfactant nanodispersions are shown to be effective in modulating the polar and dispersive components of surface tension depending on the relative particle and surfactant concentrations as well as the morphological and electrostatic nature of the dispersed phases. We observe that the combined surfactant and particle colloid exhibits a similar behavior to that of the particle only case; however, the amount of modulation of the polar and dispersive constituents is found to be different from the particle alone case which brings to the forefront the mechanisms through which surfactants modulate interfacial energies in complex fluids. Accordingly, we are able to show that the observations can be merged into a form of quasi-universal trend in the trends of polar and dispersive components in spite of the non-universal character in the wetting behavior of the fluids. We analyze the different factors affecting the polar and dispersive interactions in such complex colloids, and the physics behind such complex interactions has been explained by appealing to the classical dispersion theories by London, Debye, and Keesom as well as by Derjaguin-Landau-Verwey-Overbeek theory. The findings shed light on the nature of wetting behavior of such complex fluids and help in predicting the wettability and the degree of

Clay dispersibility and soil friability – testing the soil clay-to-carbon saturation concept

OpenAIRE

Schjønning, P.; de Jonge, L.W.; Munkholm, L.J.; Moldrup, P.; Christensen, B.T.; Olesen, J.E.

2011-01-01

Soil organic carbon (OC) influences clay dispersibility, which affects soil tilth conditions and the risk of vertical migration of clay colloids. No universal lower threshold of OC has been identified for satisfactory stabilization of soil structure. We tested the concept of clay saturation with OC as a predictor of clay dispersibility and soil friability. Soil was sampled three years in a field varying in clay content (~100 to ~220 g kg-1 soil) and grown with different crop rotations. Clay ...

Colloid mobilization and transport during capillary fringe fluctuations.

Science.gov (United States)

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

2014-07-01

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

Stabilization of silica nanoparticles dispersions by surface modification with silicon derivative of thiacalix[4]arene

Energy Technology Data Exchange (ETDEWEB)

Gorbachuk, Vladimir V.; Ziatdinova, Ramilia V. [Kazan Federal University, A.M. Butlerov’ Chemical Institute (Russian Federation); Evtugyn, Vladimir G. [Kazan Federal University, Interdisciplinary Centre for Analytical Microscopy (Russian Federation); Stoikov, Ivan I., E-mail: ivan.stoikov@mail.ru [Kazan Federal University, A.M. Butlerov’ Chemical Institute (Russian Federation)

2015-03-15

For the first time, silica nanopowder functionalized with thiacalixarene derivatives was synthesized by ultrasonication of nanoparticles (diameter 23.7 ± 2.4 nm) with organosilicon derivative of thiacalixarene in glacial acetic acid. The protocol resulted in the formation of colloidal solution of low-disperse (polydispersity index of 0.11) submicron-sized (diameter 192.5 nm) clusters of nanoparticles according to the dynamic light scattering data. As defined by scanning electron microscopy (SEM), mean diameter of thiacalixarene-functionalized nanoparticles is equal to 25.5 ± 2.5 nm and the shape is close to spherical. SEM images confirm low aggregation of thiacalixarene-modified nanoparticle compared to initial silica nanopowder (mean diameter of aggregates 330 and 429 nm, correspondingly). According to the thermogravimetry/differential scanning calorimetry and elemental analysis of the nanoparticles obtained, 5 % of the powder mass was related to thiacalixarene units. The effect of thiacalixarene functionalization of silica nanoparticles on linear polydimethylsiloxane (PDMS)—silica dispersions was modeled to achieve high resistance toward liquid media required for similar sol–gel prepared PDMS-based materials applied for solid-phase microextraction. In such a manner, the influence of thiacalixarene-modified nanofiller on thermal stability and resistance against polar organic solvents was estimated. Similarity of decomposition temperature of both thiacalixarene-functionalized nanoparticles and non-functionalized silica nanoparticles was found. Swelling/solubility behavior observed was related to partial dissolution of PDMS/silica (10 % mixture) in alcohols. Thiacalixarene-functionalized silica particles exerted significantly higher resistance of PDMS/silica composites toward alcohol solvents.

Stabilization of silica nanoparticles dispersions by surface modification with silicon derivative of thiacalix[4]arene

International Nuclear Information System (INIS)

Gorbachuk, Vladimir V.; Ziatdinova, Ramilia V.; Evtugyn, Vladimir G.; Stoikov, Ivan I.

2015-01-01

For the first time, silica nanopowder functionalized with thiacalixarene derivatives was synthesized by ultrasonication of nanoparticles (diameter 23.7 ± 2.4 nm) with organosilicon derivative of thiacalixarene in glacial acetic acid. The protocol resulted in the formation of colloidal solution of low-disperse (polydispersity index of 0.11) submicron-sized (diameter 192.5 nm) clusters of nanoparticles according to the dynamic light scattering data. As defined by scanning electron microscopy (SEM), mean diameter of thiacalixarene-functionalized nanoparticles is equal to 25.5 ± 2.5 nm and the shape is close to spherical. SEM images confirm low aggregation of thiacalixarene-modified nanoparticle compared to initial silica nanopowder (mean diameter of aggregates 330 and 429 nm, correspondingly). According to the thermogravimetry/differential scanning calorimetry and elemental analysis of the nanoparticles obtained, 5 % of the powder mass was related to thiacalixarene units. The effect of thiacalixarene functionalization of silica nanoparticles on linear polydimethylsiloxane (PDMS)—silica dispersions was modeled to achieve high resistance toward liquid media required for similar sol–gel prepared PDMS-based materials applied for solid-phase microextraction. In such a manner, the influence of thiacalixarene-modified nanofiller on thermal stability and resistance against polar organic solvents was estimated. Similarity of decomposition temperature of both thiacalixarene-functionalized nanoparticles and non-functionalized silica nanoparticles was found. Swelling/solubility behavior observed was related to partial dissolution of PDMS/silica (10 % mixture) in alcohols. Thiacalixarene-functionalized silica particles exerted significantly higher resistance of PDMS/silica composites toward alcohol solvents

Colloidal stability, surface characterisation and intracellular accumulation of Rhodium(II) citrate coated superparamagnetic iron oxide nanoparticles in breast tumour: a promising platform for cancer therapy

Energy Technology Data Exchange (ETDEWEB)

Silva Nunes, Eloiza da [Universidade Federal de Goias, Campus Samambaia, Instituto de Quimica (Brazil); Lemos Brettas Carneiro, Marcella; Guirelli Simoes de Oliveira, Ricardo; Nair Bao, Sonia [Universidade de Brasilia (UnB), Instituto de Ciencias Biologicas (Brazil); Ribeiro de Souza, Aparecido, E-mail: ardsouza@quimica.ufg.br [Universidade Federal de Goias, Campus Samambaia, Instituto de Quimica (Brazil)

2013-06-15

The colloidal stability of a rhodium(II) citrate, Rh{sub 2}(H{sub 2}cit){sub 4}, coating on the surface of maghemite ({gamma}-Fe{sub 2}O{sub 3}) nanoparticles was studied and compared in different dispersion media. The adsorption of Rh{sub 2}(H{sub 2}cit){sub 4} at the water-maghemite interface was evaluated as a function of pH and complex concentration. A slight pH-dependent adsorption of the complex was observed with a maximum at pH 3. The colloidal stability of the functionalised nanoparticles with different amounts of Rh{sub 2}(H{sub 2}cit){sub 4} as a function of pH was evaluated using dynamic light scattering measurements. The particles have a mean magnetic core size of 5.6 nm and the hydrodynamic diameters are approximately 60 nm, which remained unchanged in the pH range in which the samples were a stable sol. The tolerance to different dispersion media, which were deionised water, saline, phosphate-buffered saline (PBS), foetal bovine serum (FBS) and NaCl solutions with different concentrations, was investigated. At moderate ionic strength, the colloidal stability of the dispersions was similar in saline and in PBS compared to the stability of dispersions diluted in water. Moreover, the intracellular accumulation of nanoparticles in 4T1 breast tumour was examined by ultrastructural analysis performed by transmission electron microscopy. The rhodium(II) citrate-coated nanoparticles were found mostly in the cytoplasm and nucleus. Thus, we suggest that these SPIO nanoparticles functionalized with Rh{sub 2}(H{sub 2}Cit){sub 4} can be potential tools for anticancer therapy.

Colloid migration in porous media

International Nuclear Information System (INIS)

Hunt, J.R.; McDowell-Boyer; Sitar, N.

1985-01-01

Retention of radionuclides for long periods near waste repositories depends upon multiple barriers, one of which is adsorption to immobile solid surfaces. Since small particles and colloidal matter have high adsorption capacities per unit mass and can be mobile in subsurface flows, colloidal transport of waste components requires analysis. Theories for predicting colloid migration through porous media have been developed in the filtration literature. The applicability of filtration theories for predicting particle and colloid transport. Emphasis is on suspended matter much smaller than pore sizes, where physical and chemical forces control migration rather than size dependent physical straining. In general, experimentally verifiable theories exist for particle filtration by clean media, and a sensitivity analysis is possible on particle and media properties and fluid flow rate. When particle aggregates accumulate within pores, media permeability decreases, resulting in flow field alteration and possible radionuclide isolation. An analysis of the limited experimental data available indicates that present theories cannot predict long-term colloid transport when permeability reduction occurs. The coupling of colloid attachment processes and the hydrologic flow processes requires more extensive laboratory field research than has currently been carried out. An emphasis on the fundamental mechanisms is necessary to enhance long-term predictability

Simulation of bentonite colloid migration through granite

International Nuclear Information System (INIS)

Rosicka, Dana; Hokr, Milan

2012-01-01

Document available in extended abstract form only. Full text of publication follows: Colloidal bentonite particles generate at the interface of buffer and host rock in spent nuclear fuel repository due to an erosion process and migrate through granite by the water flow. Stability of these colloids and their migration possibilities have been studied on account of radionuclide transport possibility as colloid could carry adsorbed radionuclides in groundwater through granite. That is why a simulation of bentonite colloid migration in the surrounding of a repository might be requested. According to chemical condition as ionic strength and pH, the colloidal particles coagulate into clusters and that influence the migration of particles. The coagulation kinetics of natural bentonite colloids were experimentally studied in many articles, for example by light scattering techniques. We created a model of coagulation of bentonite colloids and simulation of a chosen experiment with use of the multicomponent reactive transport equation. The coagulation model describes clustering of particles due to attractive van der Waals forces as result of collision of particles due to heat fluctuation and different velocity of particles during sedimentation and velocity gradient of water flow. Next, the model includes influence of repulsive electrostatic forces among colloidal particles leading to stability of particles provided high surface charge of colloids. In the model, each group of clusters is transported as one solution component and the kinetics of coagulation are implemented as reactions between the components: a shift of particles among groups of particles with similar migration properties, according to size of the clusters of colloids. The simulation of migration of bentonite colloid through granite using the coagulation model was calibrated according to experiment results. On the basis of the simulation, one can estimate the basic processes that occur during bentonite colloid

Controlling electrical percolation in multicomponent carbon nanotube dispersions.

Science.gov (United States)

Kyrylyuk, Andriy V; Hermant, Marie Claire; Schilling, Tanja; Klumperman, Bert; Koning, Cor E; van der Schoot, Paul

2011-04-10

Carbon nanotube reinforced polymeric composites can have favourable electrical properties, which make them useful for applications such as flat-panel displays and photovoltaic devices. However, using aqueous dispersions to fabricate composites with specific physical properties requires that the processing of the nanotube dispersion be understood and controlled while in the liquid phase. Here, using a combination of experiment and theory, we study the electrical percolation of carbon nanotubes introduced into a polymer matrix, and show that the percolation threshold can be substantially lowered by adding small quantities of a conductive polymer latex. Mixing colloidal particles of different sizes and shapes (in this case, spherical latex particles and rod-like nanotubes) introduces competing length scales that can strongly influence the formation of the system-spanning networks that are needed to produce electrically conductive composites. Interplay between the different species in the dispersions leads to synergetic or antagonistic percolation, depending on the ease of charge transport between the various conductive components.

Wave oscillations in colloid oxyhydrates wave oscillations in colloid oxyhydrates

CERN Document Server

Sucharev, Yuri I

2010-01-01

The importance of coherent chemistry, that is, the chemistry of periodic oscillatory processes, is increasing at a rapid rate in specific chemical disciplines. While being perfectly understood and highly developed in the fields of physical chemistry, chemical physics and biological chemistry, the periodic developmental paradigm of processes and phenomena still remains poorly developed and misunderstood in classical inorganic chemistry and related branches, such as colloid chemistry. The probability is that we miss subtle colloid chemical phenomena that could be of utmost importance if taken into consideration when catalysis or adsorption is involved. The author here reveals all of the astonishing vistas that periodic wave paradigms open up to researchers in certain colloid chemical systems, and will doubtless stimulate researchers to look at them in a new light.Review from Book News Inc.: Coherent chemistry, the chemistry of periodical oscillatory processes, is well established in physical chemistry, chemical...

Coulomb force directed single and binary assembly of nanoparticles from aqueous dispersions by AFM nanoxerography.

Science.gov (United States)

Palleau, Etienne; Sangeetha, Neralagatta M; Viau, Guillaume; Marty, Jean-Daniel; Ressier, Laurence

2011-05-24

We present a simple protocol to obtain versatile assemblies of nanoparticles from aqueous dispersions onto charge patterns written by atomic force microscopy, on a 100 nm thin film of polymethylmethacrylate spin-coated on silicon wafers. This protocol of nanoxerography uses a two-stage development involving incubation of the desired aqueous colloidal dispersion on charge patterns and subsequent immersion in an adequate water-soluble alcohol. The whole process takes only a few minutes. Numerical simulations of the evolution of the electric field generated by charge patterns in various solvents are done to resolve the mechanism by which nanoparticle assembly occurs. The generic nature of this protocol is demonstrated by constructing various assemblies of charged organic/inorganic/metallic (latex, silica, gold) nanoparticles of different sizes (3 to 100 nm) and surface functionalities from aqueous dispersions onto charge patterns of complex geometries. We also demonstrate that it is possible to construct a binary assembly of nanoparticles on a pattern made of positive and negative charges generated in a single charge writing step, by sequential developments in two aqueous dispersions of oppositely charged particles. This protocol literally extends the spectra of eligible colloids that can be assembled by nanoxerography and paves the way for building complex assemblies of nanoparticles on predefined areas of surfaces, which could be useful for the elaboration of nanoparticle-based functional devices.

Magnetic field dependence observed by 27 Al NMR of species contained in alumina colloidal dispersions

International Nuclear Information System (INIS)

Morgado Junior, Edisson; Menezes, Sonia M.C.; San Gil, Rosane

1995-01-01

The behaviour of some aluminium species front a magnetic field have been investigated by 27 Al NMR analysis, this method was used for characterization of an octahedric aluminium specie from sols prepared by bohemite acid peptization. X-ray diffraction data have identified the mineral structure. The results have been shown and discussed, and NMR spectra were also presented and studied. Concluding this work, the nature of a colloidal specie of alumina was clarified through the dependence research of magnetic field by 27 Al NMR

The Effects of Subsurface Bioremediation on Soil Structure, Colloid Formation, and Contaminant Transport

Science.gov (United States)

Wang, Y.; Liang, X.; Zhuang, J.; Radosevich, M.

2016-12-01

Anaerobic bioremediation is widely applied to create anaerobic subsurface conditions designed to stimulate microorganisms that degrade organic contaminants and immobilize toxic metals in situ. Anaerobic conditions that accompany such techniques also promotes microbially mediated Fe(III)-oxide mineral reduction. The reduction of Fe(III) could potentially cause soil structure breakdown, formation of clay colloids, and alternation of soil surface chemical properties. These processes could then affect bioremediation and the migration of contaminants. Column experiments were conducted to investigate the impact of anaerobic bioreduction on soil structure, hydraulic properties, colloid formation, and transport of three tracers (bromide, DFBA, and silica shelled silver nanoparticles). Columns packed with inoculated water stable soil aggregates were placed in anaerobic glovebox, and artificial groundwater media was pumped into the columns to simulate anaerobic bioreduction process for four weeks. Decent amount of soluble Fe(II) accompanied by colloids were detected in the effluent from bioreduction columns a week after initiation of bioreduction treatment, which demonstrated bioreduction of Fe(III) and formation of colloids. Transport experiments were performed in the columns before and after bioreduction process to assess the changes of hydraulic and surface chemical properties through bioreduction treatment. Earlier breakthrough of bromide and DFBA after treatment indicated alterations in flow paths (formation of preferential flow paths). Less dispersion of bromide and DFBA, and less tailing of DFBA after treatment implied breakdown of soil aggregates. Dramatically enhanced transport and early breakthrough of silica shelled silver nanoparticles after treatment supported the above conclusion of alterations in flow paths, and indicated changes of soil surface chemical properties.

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.

Spectral characteristics and colloidal properties of chlorophyll a{prime} in aqueous methanol

Energy Technology Data Exchange (ETDEWEB)

Oba, Toru [Ritsumeikan Univ., Kusatsu (Japan); Mimuro, Mamoru [National Inst. for Basic Biology, Okazaki (Japan); Wang, Z.Y.; Nozawa, Tsunenori [Tohoku Univ., Sendai (Japan); Yoshida, Shoichiro; Watanabe, Tadashi [Univ. of Tokyo (Japan)

1997-04-17

The `phase behavior` of chlorophyll a` (Chl a`, C13{sup 2}-epimer of Chl a) dissolved in aqueous methanol was examined in terms of the composition of the solvent. The study aimed at elucidating the property of Chl a`, the exotic pigment found in a photosynthetic reaction center complex, as well as at clarifying the nature of the Chl aggregation in aqueous media. Visible absorption, circular dichroism (CD), fluorescence and resonance Raman spectroscopies, dynamic light-scattering measurements, and electron microscopy were utilized. Chl a` formed either of two types of colloids depending on the solvent composition. The one formed over a wide methanol volume percentage (ca. 73-30%) commonly possessed a single microscopic structural unit that yielded the double-peaked absorption (ca. 690 and 715 nm) accompanied by a symmetric dispersed-type CD spectrum. Increasing methanol concentration within this solvent composition range enhanced the size of the colloid and finally caused critical opalescence, which was reminiscent of the critical behavior of the aqueous solution of nonionic surfactants. These findings indicate that the microscopic structure of the Chl a` aggregate was independent of the size and shape of the colloid. The difference between the aggregation behaviors of Chl a and a` suggests a narrower choice of possible molecular arrangements in the Chl a` aggregate as an inherent property of the pigment. 37 refs., 11 figs.

Optical and structural properties of ensembles of colloidal Ag{sub 2}S quantum dots in gelatin

Energy Technology Data Exchange (ETDEWEB)

Ovchinnikov, O. V., E-mail: Ovchinnikov-O-V@rambler.ru; Smirnov, M. S. [Voronezh State University (Russian Federation); Shapiro, B. I. [Moscow State University of Fine Chemical Technologies (Russian Federation); Shatskikh, T. S.; Perepelitsa, A. S.; Korolev, N. V. [Voronezh State University (Russian Federation)

2015-03-15

The size dependences of the absorption and luminescence spectra of ensembles of hydrophilic colloidal Ag{sub 2}S quantum dots produced by the sol-gel method and dispersed in gelatin are analyzed. By X-ray diffraction analysis and transmission electron microscopy, the formation of core/shell nanoparticles is detected. The characteristic feature of the nanoparticles is the formation of crystalline cores, 1.5–2.0 nm in dimensions, and shells of gelatin and its complexes with the components of synthesis. The observed slight size dependence of the position of infrared photoluminescence bands (in the range 1000–1400 nm) in the ensembles of hydrophilic colloidal Ag{sub 2}S quantum dots is explained within the context of the model of the radiative recombination of electrons localized at structural and impurity defects with free holes.

Preparation of radioactive colloidal gold 198Au

International Nuclear Information System (INIS)

Cammarosano, S.A.

1979-01-01

The preparation with simple equipment of radioactive colloidal gold of particle size about approximately 300 A from seed colloid stabilized by gelatine is described. Some physico-chemical parameters which can affect the process of formation of these colloidal particles are analysed; particle size has been meassured with an electron microscope. The colloid stability has been studied as a function of dilution, age and pH. Nucleation and growth of radioactive colloidal gold have been studied using spectrophotometry. Absorption spectra of the two ones are presented and compared. Quality control of the production process is verified through measurement of parameters, such as radioactive and radiochemical purity and biological distribution in laboratorial animals. This distribution was evalusted for rats injected endovenously with the gold colloidal solution.(Author) [pt

Saturated Zone Colloid-Facilitated Transport

International Nuclear Information System (INIS)

Wolfsberg, A.; Reimus, P.

2001-01-01

The purpose of the Saturated Zone Colloid-Facilitated Transport Analysis and Modeling Report (AMR), as outlined in its Work Direction and Planning Document (CRWMS MandO 1999a), is to provide retardation factors for colloids with irreversibly-attached radionuclides, such as plutonium, in the saturated zone (SZ) between their point of entrance from the unsaturated zone (UZ) and downgradient compliance points. Although it is not exclusive to any particular radionuclide release scenario, this AMR especially addresses those scenarios pertaining to evidence from waste degradation experiments, which indicate that plutonium and perhaps other radionuclides may be irreversibly attached to colloids. This report establishes the requirements and elements of the design of a methodology for calculating colloid transport in the saturated zone at Yucca Mountain. In previous Total Systems Performance Assessment (TSPA) analyses, radionuclide-bearing colloids were assumed to be unretarded in their migration. Field experiments in fractured tuff at Yucca Mountain and in porous media at other sites indicate that colloids may, in fact, experience retardation relative to the mean pore-water velocity, suggesting that contaminants associated with colloids should also experience some retardation. Therefore, this analysis incorporates field data where available and a theoretical framework when site-specific data are not available for estimating plausible ranges of retardation factors in both saturated fractured tuff and saturated alluvium. The distribution of retardation factors for tuff and alluvium are developed in a form consistent with the Performance Assessment (PA) analysis framework for simulating radionuclide transport in the saturated zone. To improve on the work performed so far for the saturated-zone flow and transport modeling, concerted effort has been made in quantifying colloid retardation factors in both fractured tuff and alluvium. The fractured tuff analysis used recent data

In vivo biodegradation of colloidal quantum dots by a freshwater invertebrate, Daphnia magna

Energy Technology Data Exchange (ETDEWEB)

Kwon, Dongwook; Kim, Min Jung; Park, Chansik; Park, Jaehong [Department of Chemistry, Hanyang University, Seoul 133-791 (Korea, Republic of); Choi, Kyungho [Department of Environmental Health, Seoul National University, Seoul 151-742 (Korea, Republic of); Yoon, Tae Hyun, E-mail: thyoon@gmail.com [Department of Chemistry, Hanyang University, Seoul 133-791 (Korea, Republic of)

2012-06-15

Impacts of planktonic invertebrate, Daphnia magna, on the speciation of colloidal quantum dots (QD) were investigated using fluorescence spectromicroscopic technique. Well-dispersed {sup GA/TOPO}QD were prepared by forming a supramolecular assembly of hydrophobic {sup TOPO}QD with biomacromolecules (i.e., Gum Arabic, GA). Biological degradation of this nanomaterial was monitored by fluorescence spectromicroscopic methods. Our study confirmed the major uptake pathway of manufactured nanomaterials and in vivo biodegradation processes in a well-known toxicity test organism, D. magna. In addition, we also found that D. magna can induce significant deterioration of aquatic media by releasing fragments of partially degraded QD colloids. These biological processes may significantly change the predicted toxicities of nanomaterials in aquatic environments. Thus, we propose that the impacts of aquatic living organisms on the environmental fate of manufactured nanomaterials (MNs) should be carefully taken into account when assessing the risk of MNs to the environment and human health.

Extraordinary Hall-effect in colloidal magnetic nanoparticle films

Energy Technology Data Exchange (ETDEWEB)

Ben Gur, Leah; Tirosh, Einat [School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 6997801 (Israel); Segal, Amir [School of Physics, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 6997801 (Israel); Markovich, Gil, E-mail: gilmar@post.tau.ac.il [School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 6997801 (Israel); Gerber, Alexander, E-mail: gerber@post.tau.ac.il [School of Physics, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 6997801 (Israel)

2017-03-15

Colloidal nickel nanoparticles (NPs) coated with polyvinylpyrrolidone (PVP) were synthesized. The nanoparticle dispersions were deposited on substrates and dried under mild heating to form conductive films. The films exhibited very small coercivity, nearly metallic conductivity, and a significant extraordinary Hall effect signal. This method could be useful for preparing simple, printed magnetic field sensors with the advantage of relatively high sensitivity around zero magnetic field, in contrast to magnetoresistive sensors, which have maximal field sensitivity away from zero magnetic field. - Highlights: • Ni nanoparticle ink capable of forming conductive films on drying. • The Ni nanoparticle films exhibit significant extraordinary Hall effect. • This system could be used for preparing printed magnetic field sensors integrated in 3D printed structures.

Paclitaxel-Nanodiamond Nanocomplexes Enhance Aqueous Dispersibility and Drug Retention in Cells.

Science.gov (United States)

Lim, Dae Gon; Jung, Joo Hyun; Ko, Hyuk Wan; Kang, Eunah; Jeong, Seong Hoon

2016-09-14

Nanodiamonds (NDs) with 5 nm crystalline structures have been recognized as emerging carbon delivery vehicles due to their biocompatible inertness, high surface-to-volume ratio, and energy absorbance properties. In this study, carboxylated nanodiamond (ND-COOH) was reduced to hydroxylated nanodiamond (ND-OH) for stable and pH-independent colloidal dispersity. The poorly water-soluble paclitaxel (PTX) was physically loaded into ND-OH clusters, forming amorphous PTX nanostructure on the interparticle nanocage of the ND substrate. Stable physical PTX loading onto the ND substrate with stable colloidal stability showed enhanced PTX release. ND-OH/PTX complexes retained the sustained release of PTX by up to 97.32% at 70 h, compared with the 47.33% release of bare crystalline PTX. Enhanced PTX release from ND substrate showed low cell viability in Hela, MCF-9, and A549 cancer cells due to sustained release and stable dispersity in a biological aqueous environment. Especially, the IC50 values of ND-OH/PTX complexes and PTX in Hela cells were 0.037 μg/mL and 0.137 μg/mL, respectively. Well-dispersed cellular uptake of suprastructure ND-OH/PTX nanocomplexes was directly observed from the TEM images. ND-OH/PTX nanocomplexes assimilated into cells might provide convective diffusion with high PTX concentration, inducing initial necrosis. This study suggests that poorly water-soluble drugs can be formulated into a suprastructure with ND and acts as a highly concentrated drug reservoir directly within a cell.

Active structuring of colloidal armour on liquid drops

Science.gov (United States)

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

2013-06-01

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

Thermophoretic torque in colloidal particles with mass asymmetry

Science.gov (United States)

Olarte-Plata, Juan; Rubi, J. Miguel; Bresme, Fernando

2018-05-01

We investigate the response of anisotropic colloids suspended in a fluid under a thermal field. Using nonequilibrium molecular dynamics computer simulations and nonequilibrium thermodynamics theory, we show that an anisotropic mass distribution inside the colloid rectifies the rotational Brownian motion and the colloids experience transient torques that orient the colloid along the direction of the thermal field. This physical effect gives rise to distinctive changes in the dependence of the Soret coefficient with colloid mass, which features a maximum, unlike the monotonic increase of the thermophoretic force with mass observed in homogeneous colloids.

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)

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

Colloid-facilitated radionuclide transport: a regulatory perspective

Science.gov (United States)

Dam, W. L.; Pickett, D. A.; Codell, R. B.; Nicholson, T. J.

2001-12-01

What hydrogeologic-geochemical-microbial conditions and processes affect migration of radionuclides sorbed onto microparticles or native colloid-sized radionuclide particles? The U.S. Nuclear Regulatory Commission (NRC) is responsible for protecting public health, safety, and the environment at numerous nuclear facilities including a potential high-level nuclear waste disposal site. To fulfill these obligations, NRC needs to understand the mechanisms controlling radionuclide release and transport and their importance to performance. The current focus of NRC staff reviews and technical interactions dealing with colloid-facilitated transport relates to the potential nuclear-waste repository at Yucca Mountain, Nevada. NRC staff performed bounding calculations to quantify radionuclide releases available for ground-water transport to potential receptors from a Yucca Mountain repository. Preliminary analyses suggest insignificant doses of plutonium and americium colloids could be derived from spent nuclear fuel. Using surface complexation models, NRC staff found that colloids can potentially lower actinide retardation factors by up to several orders of magnitude. Performance assessment calculations, in which colloidal transport of plutonium and americium was simulated by assuming no sorption or matrix diffusion, indicated no effect of colloids on human dose within the 10,000 year compliance period due largely to long waste-package lifetimes. NRC staff have identified information gaps and developed technical agreements with the U.S. Department of Energy (DOE) to ensure sufficient information will be presented in any potential future Yucca Mountain license application. DOE has agreed to identify which radionuclides could be transported via colloids, incorporate uncertainties in colloid formation, release and transport parameters, and conceptual models, and address the applicability of field data using synthetic microspheres as colloid analogs. NRC is currently

Exploring how organic matter controls structural transformations in natural aquatic nanocolloidal dispersions.

Science.gov (United States)

King, Stephen M; Jarvie, Helen P

2012-07-03

The response of the dispersion nanostructure of surface river bed sediment to the controlled removal and readdition of natural organic matter (NOM), in the absence and presence of background electrolyte, was examined using the technique of small-angle neutron scattering (SANS). Partial NOM removal induced aggregation of the mineral particles, but more extensive NOM removal restored colloidal stability. When peat humic acid (PHA) was added to a NOM-deficient sediment concentration-related structural transformations were observed: at 255 mg/L PHA aggregation of the nanocolloid was actually enhanced, but at 380 mg/L PHA disaggregation and colloidal stability were promoted. The addition of 2 mM CaCl(2) induced mild aggregation in the native sediment but not in sediments with added PHA, suggesting that the native NOM and the PHA respond differently to changes in ionic strength. A first attempt at using SANS to directly characterize the thickness and coverage of an adsorbed PHA layer in a natural nanocolloid is also presented. The results are discussed in the context of a hierarchical aquatic colloidal nanostructure, and the implications for contemporary studies of the role of dissolved organic carbon (DOC) in sustaining the transport of colloidal iron in upland catchments.

Recommendations for plutonium colloid size determination

International Nuclear Information System (INIS)

Kosiewicz, S.T.

1984-02-01

This report presents recommendations for plutonium colloid size determination and summarizes a literature review, discussions with other researchers, and comments from equipment manufacturers. Four techniques suitable for plutonium colloid size characterization are filtration and ultrafiltration, gel permeation chromatography, diffusion methods, and high-pressure liquid chromatography (conditionally). Our findings include the following: (1) Filtration and ultrafiltration should be the first methods used for plutonium colloid size determination because they can provide the most rapid results with the least complicated experimental arrangement. (2) After expertise has been obtained with filtering, gel permeation chromatography should be incorporated into the colloid size determination program. (3) Diffusion methods can be used next. (4) High-pressure liquid chromatography will be suitable after appropriate columns are available. A plutonium colloid size characterization program with filtration/ultrafiltration and gel permeation chromatography has been initiated

Colloidal stability of Ni(OH){sub 2} in water and its dispersion into a ceramic matrix from the reaction media to obtain Ni/Al{sub 2}O{sub 3} materials

Energy Technology Data Exchange (ETDEWEB)

Cabanas-Polo, S.; Ferrari, B.; Sanchez-Herencia, A. J.

2014-07-01

Ni/Al{sub 2}O{sub 3} composites have been fabricated by slip casting of concentrated Ni(OH){sub 2}/Al{sub 2}O{sub 3} suspensions and subsequent in situ reduction to metallic nickel during sintering. For that, the synthesis assisted by ultrasound of both α- and β-Ni(OH){sub 2} polymorphs, as well as their colloidal stability, have been studied. The structural differences between both polymorphs have been thoroughly studied by means of XRD, FTIR, DTA-TG, SSA, SEM and TEM, in order to optimize the starting suspensions. This way, the IEP of both polymorphs have been established (9.7 y 12 for β- and α-Ni(OH){sub 2}, respectively), as well as the optimal content of an anionic dispersant (PAA) to stabilize the particles (0.8 wt. % for beta phase and 3.0 wt. % for alpha phase). Three different Ni/Al{sub 2}O{sub 3} composites, with a high dispersion degree of the metallic phase, have been obtained considering the potential vs. particles distance curve of the Ni(OH){sub 2}, and their structure has been discussed in terms of the strength of the agglomerates and/or aggregates of the Ni(OH){sub 2}. (Author)

Quantum-size colloid metal systems

International Nuclear Information System (INIS)

Roldugin, V.I.

2000-01-01

In the review dealing with quantum-dimensional metallic colloid systems the methods of preparation, electronic, optical and thermodynamic properties of metal nanoparticles and thin films are considered, the effect of ionizing radiation on stability of silver colloid sols and existence of a threshold radiation dose affecting loss of stability being discussed. It is shown that sol stability loss stems from particles charge neutralization due to reduction of sorbed silver ions induced by radiation, which results in destruction of double electric layer on colloid particles boundary [ru

FEBEX bentonite colloid stability in ground water

Energy Technology Data Exchange (ETDEWEB)

Seher, H.; Schaefer, T.; Geckeis, H. [Inst. fuer Nukleare Entsorgung (INE), Forschungszentrum Karlsruhe, 76021 Karlsruhe (Germany)]. e-mail: holger.seher@ine.fzk .de; Fanghaenel, T. [Ruprecht-Karls-Univ. Heidelberg, Physikalisch-Chemisches In st., D-69120 Heidelberg (Germany)

2007-06-15

Coagulation experiments are accomplished to identify the geochemical conditions for the stability of Febex bentonite colloids in granite ground water. The experiments are carried out by varying pH, ionic strength and type of electrolyte. The dynamic light scattering technique (photon correlation spectroscopy) is used to measure the size evolution of the colloids with time. Agglomeration rates are higher in MgCl{sub 2} and CaCl{sub 2} than in NaCl solution. Relative agglomeration rates follow approximately the Schulze-Hardy rule. Increasing agglomeration rates at pH>8 are observed in experiments with MgCl{sub 2} and CaCl{sub 2} which are, however, caused by coprecipitation phenomena. Bentonite colloid stability fields derived from the colloid agglomeration experiments predict low colloid stabilization in granite ground water taken from Aespoe, Sweden, and relatively high colloid stability in Grimsel ground water (Switzerland)

Modeling of the geochemical behaviour and of the radionuclide transport in the presence of colloids

International Nuclear Information System (INIS)

Van der Lee, Jan

1997-01-01

CHESS, a complete geochemical model, especially developed for coupling purposes in a transparent manner with transport codes. The second topic concerns the development of a probabilistic theory for colloid retention, as well as for the kinetics involved in the reaction. The proposed theory seem to be robust, predicts correctly the impact of System parameters such as pH, ionic strength and colloid size, and is applicable to real Systems, at least at the scale of laboratory experiments. The thesis also presents the theory of adsorption kinetics. This theory is more rigorous than the theories available in the literature, and applies for porous as well as fractured media. A comparison with models provided by the literature and with experimental data seems to confirm the correctness of the theory. The third topic involves reactive transport modelling of chemical species and colloids and has lead to the development of a new transport model, HYTEC. This tool includes convective-diffusive-dispersive transport of colloids, aqueous species and gases, calculates the thermodynamic equilibrium state of the solution and incorporates the newly developed theory of colloid retention. As far as we know, this is the first model which integrates colloids as well as the complete geochemistry in a transport model. Resuming, this work shows the importance of the adsorption capacity of most of the natural colloids with respect to actinides, such as uranium, americium and europium. The complexation capacity of organic colloids is even greater than that of inorganic colloids, such as silica, clays and hydrous ferric oxide. This study also indicates that colloids are capable of keeping the radioactive load during their journey through the geological medium, even if the complexing affinity of the medium is much stronger than of the colloids. Accordingly, colloids may act as a very rapid transport vehicle for radionuclides, provided they are chemically and electrostatically stable in suspension

Use of polysulfides of alkali and alkaline-earth metals to obtain highly dispersed sulfur

International Nuclear Information System (INIS)

Massalimov, I.A.; Vikhareva, I.N.; Kireeva, M.S.

2008-01-01

Possibilities of obtaining polysulfides of alkali and alkaline earth metals (M is Na, K, Ca, Sr, Ba) in aqueous solutions were considered. The composition of the polysulfides and their concentration in solutions were found. The efficiencies of application of highly dispersed sulfur, produced from calcium polysulfide, and colloid sulfur as a fungicide were compared [ru

Interface colloidal robotic manipulator

Science.gov (United States)

Aronson, Igor; Snezhko, Oleksiy

2015-08-04

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

Synthesis of pure colloidal silver nanoparticles with high electroconductivity for printed electronic circuits: the effect of amines on their formation in aqueous media.

Science.gov (United States)

Natsuki, Jun; Abe, Takao

2011-07-01

This paper describes a practical and convenient method to prepare stable colloidal silver nanoparticles for use in printed electronic circuits. The method uses a dispersant and two kinds of reducing agents including 2-(dimethylamino) ethanol (DMAE), which play important roles in the reduction of silver ions in an aqueous medium. The effect of DMAE and dispersant, as well as the factors affecting particle size and morphology are investigated. In the formation of the silver nanoparticles, reduction occurs rapidly at room temperature and the silver particles can be separated easily from the mixture in a short time. In addition, organic solvents are not used. Pure, small and relatively uniform particles with a diameter less than 10 nm can be obtained that exhibit high electroconductivity. The silver nanoparticles are stable, and can be isolated as a dried powder that can be fully redispersed in deionized water. This method of producing colloidal silver nanoparticles will find practical use in electronics applications. Copyright © 2011 Elsevier Inc. All rights reserved.

Molecular Recognition in the Colloidal World.

Science.gov (United States)

Elacqua, Elizabeth; Zheng, Xiaolong; Shillingford, Cicely; Liu, Mingzhu; Weck, Marcus

2017-11-21

Colloidal self-assembly is a bottom-up technique to fabricate functional nanomaterials, with paramount interest stemming from programmable assembly of smaller building blocks into dynamic crystalline domains and photonic materials. Multiple established colloidal platforms feature diverse shapes and bonding interactions, while achieving specific orientations along with short- and long-range order. A major impediment to their universal use as building blocks for predesigned architectures is the inability to precisely dictate and control particle functionalization and concomitant reversible self-assembly. Progress in colloidal self-assembly necessitates the development of strategies that endow bonding specificity and directionality within assemblies. Methodologies that emulate molecular and polymeric three-dimensional (3D) architectures feature elements of covalent bonding, while high-fidelity molecular recognition events have been installed to realize responsive reconfigurable assemblies. The emergence of anisotropic 'colloidal molecules', coupled with the ability to site-specifically decorate particle surfaces with supramolecular recognition motifs, has facilitated the formation of superstructures via directional interactions and shape recognition. In this Account, we describe supramolecular assembly routes to drive colloidal particles into precisely assembled architectures or crystalline lattices via directional noncovalent molecular interactions. The design principles are based upon the fabrication of colloidal particles bearing surface-exposed functional groups that can undergo programmable conjugation to install recognition motifs with high fidelity. Modular and versatile by design, our strategy allows for the introduction and integration of molecular recognition principles into the colloidal world. We define noncovalent molecular interactions as site-specific forces that are predictable (i.e., feature selective and controllable complementary bonding partners

Boiling of water in flow restricted areas modeled by colloidal silica deposits

International Nuclear Information System (INIS)

Peixinho, Jorge; Lefevre, Gregory; Coudert, Francois-Xavier; Hurisse, Olivier

2012-09-01

Understanding the effects of particle deposits on evaporation and boiling of water represents an important issue for EDF because it causes a severe reduction in efficiency particularly in steam generators of pressurized water reactor. These deposits are made of oxide metallic particles and the deposition process depends on multiple factors. Here we mimic deposits using a simple system made of hydrophilic silica particles. The present study reports experiments on evaporation or boiling of water confined in the pores of colloidal mono-dispersed silica micro-sphere deposits. The boiling of water confined in the pores of the colloidal crystal is studied using optical microscopy, scanning electron microscopy, nitrogen adsorption, water adsorption through infrared attenuated total reflectance spectroscopy, differential scanning calorimetry and thermal gravimetric analysis. By comparison of the results with silica deposits and alumina membranes with cylindrical pores, our study shows that the morphology of the pores contributes to the evaporation and boiling of water. The measurements suggest that particle resuspension and crust formation take place during drying at elevated temperature and are responsible for cracks formation within the deposit film. (authors)

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.)

One-pot synthesis of stable colloidal solutions of MFe2O4 nanoparticles using oleylamine as solvent and stabilizer

International Nuclear Information System (INIS)

Pérez-Mirabet, Leonardo; Solano, Eduardo; Martínez-Julián, Fernando; Guzmán, Roger; Arbiol, Jordi; Puig, Teresa; Obradors, Xavier; Pomar, Alberto; Yáñez, Ramón; Ros, Josep; Ricart, Susagna

2013-01-01

Highlights: ► One-pot synthesis of ferrite magnetic nanoparticles ( 3 and M(acac) 2 (M = Co, Mn, Cu and Zn) in oleylamine, which also acts as a capping ligand, by producing stable colloidal dispersions of nanoparticles in non-polar solvents. The properties of the nanoparticles have been studied via different techniques, such as transmission electron microscopy, which shows that nanoparticles are monocrystallines and a narrow dispersion in size; magnetic analyses have demonstrated that the resulting ferrite nanoparticles show high saturation values and superparamagnetic behavior at room temperature; X-ray diffraction has also been performed, and it confirms that the synthesized nanoparticles have a spinel structure. Complementarily, ligand exchange has been also carried out in order to produce dispersions of the synthesized nanoparticles in polar media

Horseradish peroxidase-nanoclay hybrid particles of high functional and colloidal stability.

Science.gov (United States)

Pavlovic, Marko; Rouster, Paul; Somosi, Zoltan; Szilagyi, Istvan

2018-08-15

Highly stable dispersions of enzyme-clay nanohybrids of excellent horseradish peroxidase activity were developed. Layered double hydroxide nanoclay was synthesized and functionalized with heparin polyelectrolyte to immobilize the horseradish peroxidase enzyme. The formation of a saturated heparin layer on the platelets led to charge inversion of the positively charged bare nanoclay and to highly stable aqueous dispersions. Great affinity of the enzyme to the surface modified platelets resulted in strong horseradish peroxidase adsorption through electrostatic and hydrophobic interactions as well as hydrogen bonding network and prevented enzyme leakage from the obtained material. The enzyme kept its functional integrity upon immobilization and showed excellent activity in decomposition of hydrogen peroxide and oxidation of an aromatic compound in the test reactions. In addition, remarkable long term functional stability of the enzyme-nanoclay hybrid was observed making the developed colloidal system a promising antioxidant candidate in biomedical treatments and industrial processes. Copyright © 2018 Elsevier Inc. All rights reserved.

Functional Nanofibers and Colloidal Gels: Key Elements to Enhance Functionality

Science.gov (United States)

Vogel, Nancy Amanda

material so that prolonged release can be readily achieved from highly water soluble nanofibers. The final research theme focuses on gaining a fundamental understanding of a new class of materials, nanodiamond, so that a desired microstructure can be achieved via functionalization or manipulating processing parameters. In particular, we utilize both steady and dynamic rheology techniques to systematically investigate systems of nanodiamonds dispersed in model nonpolar (mineral oil) and polar (glycerol) media. In both cases, selfsupporting colloidal gels form at relatively low nanodiamond content; however, the gel behavior is highly dependent on the type of media used. Nanodiamonds dispersed in mineral oil exhibit characteristic colloidal gel behavior, with a rheological response that is independent of both frequency and time. However, nanodiamonds dispersed in glycerol exhibit a time dependent response, with the strength of the colloidal gels increasing several orders of magnitude. We attribute these rheological differences to changes in solvent complexity, where new particle-solvent and particle-particle interactions have the potential to delay optimal gel formation. In addition to colloidal gel formation, we use large oscillatory strains to probe the effect of processing parameters on microstructure disruption and recovery. The results indicate that the formation and rearrangement of the nanodiamond microstructures are concentration dependent for both media types; however, the recovery after breakdown is different for each system. Recovery of the nanodiamond/mineral oil gels is incomplete, with the strength of the recovered gel being significantly reduced. In contrast, the original strength of the nanodiamond/glycerol gels is recoverable as the system restructures with time. The practical implications of these results are significant as it suggest that shear history and solvent polarity play a dominant role in nanodiamond processing.

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.

Synthesis and colloidal properties of anisotropic hydrothermal barium titanate

Science.gov (United States)

Yosenick, Timothy James

2005-11-01

Nanoparticles of high dielectric constant materials, especially BaTiO3, are required to achieve decreased layer thickness in multilayer ceramic capacitors (MLCCs). Tabular metal nanoparticles can produce thin metal layers with low surface roughness via electrophoretic deposition (EPD). To achieve similar results with dielectric layers requires the synthesis and dispersion of tabular BaTiO3 nanoparticles. The goal of this study was to investigate the deposition of thin BaTiO3 layers using a colloidal process. The synthesis, interfacial chemistry and colloidal properties of hydrothermal BaTiO3 a model particle system, was investigated. After characterization of the material system particulates were deposited to form thin layers using EPD. In the current study, the synthesis of BaTiO3 has been investigated using a hydrothermal route. TEM and AFM analyses show that the synthesized particles are single crystal with a majority of the particle having a zone axis and {111} large face. The particles have a median thickness of 5.8 +/- 3.1 nm and face diameter of 27.1 +/- 12.3 nm. Particle growth was likely controlled by the formation of {111} twins and the synthesis pH which stabilizes the {111} face during growth. With limited growth in the direction, the particles developed a plate-like morphology. Physical property characterization shows the powder was suitable for further processing with high purity, low hydrothermal defect concentration, and controlled stoichiometry. TEM observations of thermally treated powders indicate that the particles begin to loose the plate-like morphology by 900 °C. The aqueous passivation, dispersion, and doping of nanoscale BaTiO 3 powders was investigated. Passivation BaTiO3 was achieved through the addition of oxalic acid. The oxalic acid selectively adsorbs onto the particle surface and forms a chemically stable 2-3 nm layer of barium oxalate. The negative surface charge of the oxalate effectively passivated the BaTiO3 providing a surface

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

Science.gov (United States)

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

2016-06-28

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

Colloid-Facilitated Transport of Radionuclides Through The Vadose Zone

International Nuclear Information System (INIS)

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

2007-01-01

The main purpose of this project was to advance the basic scientific understanding of colloid and colloid-facilitated Cs transport of radionuclides in the vadose zone. We focused our research on the hydrological and geochemical conditions beneath the leaking waste tanks at the USDOE Hanford reservation. Specific objectives were (1) to determine the lability and thermodynamic stability of colloidal materials, which form after reacting Hanford sediments with simulated Hanford Tank Waste, (2) to characterize the interactions between colloidal particles and contaminants, i.e., Cs and Eu, (3) to determine the potential of Hanford sediments for in situ mobilization of colloids, (4) to evaluate colloid-facilitated radionuclide transport through sediments under unsaturated flow, (5) to implement colloid-facilitated contaminant transport mechanisms into a transport model, and (6) to improve conceptual characterization of colloid-contaminant-soil interactions and colloid-facilitated transport for clean-up procedures and long-term risk assessment

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)

Adsorption of dispersing polyelectrolytes: stabilization of drilling fluids; Adsorption de polyelectrolytes dispersants: stabilisation des fluides de forage

Energy Technology Data Exchange (ETDEWEB)

Balastre, M.

1999-11-10

Instabilities of concentrated colloidal suspensions are a source of many industrial problems, as in drilling fluid formulations where aggregation and severe settling phenomena can occur. Low molecular weight polyelectrolyte dispersants are used to solve these problems, but their optimal use requires a better understanding of the phenomena that are involved. After materials characterization, adsorption mechanisms of two anionic polyelectrolytes (PANa, PSSNa) on a soluble substrate model, barium sulfate powder are studied. Barium sulfate is the principal additive used to adapt the density of drilling fluids. A simple model allows us to propose a distribution of the microscopic species at the interface. Presence of divalent ions induces the formation of a strong complex with the polyelectrolyte. Adsorption and electro-kinetic data are presented and exchange equilibrium are examined in relation with the surface uptake. The binding mechanism and the surface speciation of the polymer groups are deduced from the ion exchange analysis. The macroscopic behavior of suspensions on different conditions (volume fraction, ionic strength, dispersant concentration) is studied by settling and rheological measurements. The macroscopic properties are connected to structural aspects, and we show that dispersing effects are mostly related to electro-steric repulsion. The dispersion state depends on two principal factors adsorbed amounts and adsorbed layer properties, especially the excess charge, and the molecules conformation. (author)

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.

Colloidal dispersions of conducting copolymers of aniline and p-phenylenediamine for films with enhanced conductometric sensitivity to temperature

Czech Academy of Sciences Publication Activity Database

Li, Yu; Bober, Patrycja; Trchová, Miroslava; Stejskal, Jaroslav

2017-01-01

Roč. 5, č. 7 (2017), s. 1668-1674 ISSN 2050-7526 R&D Projects: GA ČR(CZ) GP14-05568P Institutional support: RVO:61389013 Keywords : colloids * polyaniline * poly(p-phenylenediamine) Subject RIV: JI - Composite Materials OBOR OECD: Composites (including laminates, reinforced plastics, cermets, combined natural and synthetic fibre fabrics Impact factor: 5.256, year: 2016

Water evaporation in silica colloidal deposits.

Science.gov (United States)

Peixinho, Jorge; Lefèvre, Grégory; Coudert, François-Xavier; Hurisse, Olivier

2013-10-15

The results of an experimental study on the evaporation and boiling of water confined in the pores of deposits made of mono-dispersed silica colloidal micro-spheres are reported. The deposits are studied using scanning electron microscopy, adsorption of nitrogen, and adsorption of water through attenuated total reflection-infrared spectroscopy. The evaporation is characterized using differential scanning calorimetry and thermal gravimetric analysis. Optical microscopy is used to observe the patterns on the deposits after evaporation. When heating at a constant rate and above boiling temperature, the release of water out of the deposits is a two step process. The first step is due to the evaporation and boiling of the surrounding and bulk water and the second is due to the desorption of water from the pores. Additional experiments on the evaporation of water from membranes having cylindrical pores and of heptane from silica deposits suggest that the second step is due to the morphology of the deposits. Copyright © 2013 Elsevier Inc. All rights reserved.

Perspectives on Exertional Rhabdomyolysis.

Science.gov (United States)

Rawson, Eric S; Clarkson, Priscilla M; Tarnopolsky, Mark A

2017-03-01

Exertional (exercise-induced) rhabdomyolysis is a potentially life threatening condition that has been the subject of research, intense discussion, and media attention. The causes of rhabdomyolysis are numerous and can include direct muscle injury, unaccustomed exercise, ischemia, extreme temperatures, electrolyte abnormalities, endocrinologic conditions, genetic disorders, autoimmune disorders, infections, drugs, toxins, and venoms. The objective of this article is to review the literature on exertional rhabdomyolysis, identify precipitating factors, and examine the role of the dietary supplement creatine monohydrate. PubMed and SPORTDiscus databases were searched using the terms rhabdomyolysis, muscle damage, creatine, creatine supplementation, creatine monohydrate, and phosphocreatine. Additionally, the references of papers identified through this search were examined for relevant studies. A meta-analysis was not performed. Although the prevalence of rhabdomyolysis is low, instances still occur where exercise is improperly prescribed or used as punishment, or incomplete medical history is taken, and exertional rhabdomyolysis occurs. Creatine monohydrate does not appear to be a precipitating factor for exertional rhabdomyolysis. Healthcare professionals should be able to recognize the basic signs of exertional rhabdomyolysis so prompt treatment can be administered. For the risk of rhabdomyolysis to remain low, exercise testing and prescription must be properly conducted based on professional standards.

Dynamic Colloidal Molecules Maneuvered by Light-Controlled Janus Micromotors.

Science.gov (United States)

Gao, Yirong; Mou, Fangzhi; Feng, Yizheng; Che, Shengping; Li, Wei; Xu, Leilei; Guan, Jianguo

2017-07-12

In this work, we propose and demonstrate a dynamic colloidal molecule that is capable of moving autonomously and performing swift, reversible, and in-place assembly dissociation in a high accuracy by manipulating a TiO 2 /Pt Janus micromotor with light irradiation. Due to the efficient motion of the TiO 2 /Pt Janus motor and the light-switchable electrostatic interactions between the micromotor and colloidal particles, the colloidal particles can be captured and assembled one by one on the fly, subsequently forming into swimming colloidal molecules by mimicking space-filling models of simple molecules with central atoms. The as-demonstrated dynamic colloidal molecules have a configuration accurately controlled and stabilized by regulating the time-dependent intensity of UV light, which controls the stop-and-go motion of the colloidal molecules. The dynamic colloidal molecules are dissociated when the light irradiation is turned off due to the disappearance of light-switchable electrostatic interaction between the motor and the colloidal particles. The strategy for the assembly of dynamic colloidal molecules is applicable to various charged colloidal particles. The simulated optical properties of a dynamic colloidal molecule imply that the results here may provide a novel approach for in-place building functional microdevices, such as microlens arrays, in a swift and reversible manner.

Colloidal CdSe Quantum Rings.

Science.gov (United States)

Fedin, Igor; Talapin, Dmitri V

2016-08-10

Semiconductor quantum rings are of great fundamental interest because their non-trivial topology creates novel physical properties. At the same time, toroidal topology is difficult to achieve for colloidal nanocrystals and epitaxially grown semiconductor nanostructures. In this work, we introduce the synthesis of luminescent colloidal CdSe nanorings and nanostructures with double and triple toroidal topology. The nanorings form during controlled etching and rearrangement of two-dimensional nanoplatelets. We discuss a possible mechanism of the transformation of nanoplatelets into nanorings and potential utility of colloidal nanorings for magneto-optical (e.g., Aharonov-Bohm effect) and other applications.

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.

Effect of highly dispersed yttria addition on thermal stability of hydroxyapatite

Energy Technology Data Exchange (ETDEWEB)

Parente, P., E-mail: pparente@icv.csic.es [Instituto de Ceramica y Vidrio, CSIC, C/Kelsen 5, Madrid 28049 (Spain); Savoini, B. [Departamento de Fisica, Universidad Carlos III de Madrid, Avda. Universidad 30, Leganes 28911 (Spain); Ferrari, B. [Instituto de Ceramica y Vidrio, CSIC, C/Kelsen 5, Madrid 28049 (Spain); Monge, M.A.; Pareja, R. [Departamento de Fisica, Universidad Carlos III de Madrid, Avda. Universidad 30, Leganes 28911 (Spain); Sanchez-Herencia, A.J. [Instituto de Ceramica y Vidrio, CSIC, C/Kelsen 5, Madrid 28049 (Spain)

2013-03-01

The capability of the colloidal method to produce yttria (Y{sub 2}O{sub 3}) dispersed hydroxyapatite (HA) has been investigated as an alternative method to the conventional method of mechanical mixing and sintering for developing HA-based materials that could exhibit controllable and enhanced functional properties. A water based colloidal route to produce HA materials with highly dispersed Y{sub 2}O{sub 3} has been applied, and the effect of 10 wt.% Y{sub 2}O{sub 3} addition to HA investigated by thermal analysis, X-ray diffraction and Fourier transform infrared spectroscopy. These measurements evidence a remarkable effect of this Y{sub 2}O{sub 3} addition on decomposition mechanisms of synthetic HA. Results show that incorporation of Y{sub 2}O{sub 3} as dispersed second phase is beneficial because it hinders the decomposition mechanisms of HA into calcium phosphates. This retardation will allow the control of the sintering conditions for developing HA implants with improved properties. Besides, substitution of Ca{sup 2+} with Y{sup 3+} ions appears to promote the formation of OH{sup -} vacancies, which could improve the conductive properties of HA favorable to osseointegration. - Highlights: Black-Right-Pointing-Pointer We reveal the influence of Y{sub 2}O{sub 3} on thermal stability of hydroxyapatite. Black-Right-Pointing-Pointer Incorporation of Y{sub 2}O{sub 3} delays decomposition of hydroxyapatite to calcium phosphates. Black-Right-Pointing-Pointer Addition of Y{sub 2}O{sub 3} enables sintering conditions more favorable to the densification.

The definition of exertion-related cardiac events.

Science.gov (United States)

Rai, M; Thompson, P D

2011-02-01

Vigorous physical activity increases the risk of sudden cardiac death (SCD) and acute myocardial infarction (AMI) but there is no standard definition as to what constitutes an exertion-related cardiac event, specifically the time interval between physical exertion and cardiac event. A systematic review of studies related to exertion-related cardiac events was performed and the time interval between exertion and the event or the symptoms leading to the event was looked for in all the articles selected for inclusion. A total of 12 of 26 articles "suggested" or "defined" exertion-related events as those events whose symptoms started during or within 1 h of exertion. Others used definitions of 0.5 h, 2 h, "during exertion", "during or immediately post exertion" and "during or within several hours after exertion". It is suggested, therefore, that the definition of an exertion-related cardiac event be established as a cardiac event in which symptoms started during or within 1 h of physical exertion.

Conductivity maximum in a charged colloidal suspension

Energy Technology Data Exchange (ETDEWEB)

Bastea, S

2009-01-27

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

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

Active structuring of colloidal armour on liquid drops

OpenAIRE

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

2013-01-01

Adsorption and assembly of colloidal particles at the surface of liquid droplets are at the base of particle-stabilized emulsions and templating. Here we report that electrohydrodynamic and electro-rheological effects in leaky-dielectric liquid drops can be used to structure and dynamically control colloidal particle assemblies at drop surfaces, including electric-fieldassisted convective assembly of jammed colloidal ‘ribbons’, electro-rheological colloidal chains confined to a...

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

Radiolytic reduction reaction of colloidal silver bromide solution

International Nuclear Information System (INIS)

Oya, Yasuhisa; Zushi, Takehiro; Hasegawa, Kunihiko; Matsuura, Tatsuo.

1995-01-01

The reduction reaction of colloidal silver bromide (AgBr 3 ) 2- in nitrous oxide gas saturated solution of some alcohols: methanol, ethanol, 2-propanol and 2-methyl-2-propanol by γ-irradiation was studied spectrophotometrically in order to elucidate the mechanism of the formation of colloidal silver bromide (AgBr 3 ) 3- at ambient temperature. The amount of colloidal silver bromide formed increases in the order: i-PrOH, EtOH, MeOH. In t-BuOH, colloidal silver bromide did not form. The relative reactivities of alcohols for colloidal silver bromide was also studied kinetically. (author)

Colloid Thrusters, Physics, Fabrication and Performance

National Research Council Canada - National Science Library

Martinez-Sanchez, Manuel; Akinwande, Akintunde I

2005-01-01

... discovered pure ionic mode, the microfabrication in Silicon of two types of arrays of colloid or electrospray emitters, and the development of a quantitative theory for the colloidal regime (no ions...

Colloid-Facilitated Transport of Radionuclides through the Vadose Zone

International Nuclear Information System (INIS)

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

2006-01-01

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

Impact of Redox Reactions on Colloid Transport in Saturated Porous Media: An Example of Ferrihydrite Colloids Transport in the Presence of Sulfide.

Science.gov (United States)

Liao, Peng; Yuan, Songhu; Wang, Dengjun

2016-10-18

Transport of colloids in the subsurface is an important environmental process with most research interests centered on the transport in chemically stable conditions. While colloids can be formed under dynamic redox conditions, the impact of redox reactions on their transport is largely overlooked. Taking the redox reactions between ferrihydrite colloids and sulfide as an example, we investigated how and to what extent the redox reactions modulated the transport of ferrihydrite colloids in anoxic sand columns over a range of environmentally relevant conditions. Our results reveal that the presence of sulfide (7.8-46.9 μM) significantly decreased the breakthrough of ferrihydrite colloids in the sand column. The estimated travel distance of ferrihydrite colloids in the absence of sulfide was nearly 7-fold larger than that in the presence of 46.9 μM sulfide. The reduced breakthrough was primarily attributed to the reductive dissolution of ferrihydrite colloids by sulfide in parallel with formation of elemental sulfur (S(0)) particles from sulfide oxidation. Reductive dissolution decreased the total mass of ferrihydrite colloids, while the negatively charged S(0) decreased the overall zeta potential of ferrihydrite colloids by attaching onto their surfaces and thus enhanced their retention in the sand. Our findings provide novel insights into the critical role of redox reactions on the transport of redox-sensitive colloids in saturated porous media.

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).

Colloid transport in model fracture filling materials

Science.gov (United States)

Wold, S.; Garcia-Garcia, S.; Jonsson, M.

2010-12-01

Colloid transport in model fracture filling materials Susanna Wold*, Sandra García-García and Mats Jonsson KTH Chemical Science and Engineering Royal Institute of Technology, SE-100 44 Stockholm, Sweden *Corresponding author: E-mail: wold@kth.se Phone: +46 8 790 6295 In colloid transport in water-bearing fractures, the retardation depends on interactions with the fracture surface by sorption or filtration. These mechanisms are difficult to separate. A rougher surface will give a larger area available for sorption, and also when a particle is physically hindered, it approaches the surface and enables further sorption. Sorption can be explained by electrostatics were the strongest sorption on minerals always is observed at pH below pHpzc (Filby et al., 2008). The adhesion of colloids to mineral surfaces is related to the surface roughness according to a recent study (Darbha et al., 2010). There is a large variation in the characteristics of water-bearing fractures in bedrock in terms of aperture distribution, flow velocity, surface roughness, mineral distributions, presence of fracture filling material, and biological and organic material, which is hard to implement in modeling. The aim of this work was to study the transport of negatively charged colloids in model fracture filling material in relation to flow, porosity, mineral type, colloid size, and surface charge distribution. In addition, the impact on transport of colloids of mixing model fracture filling materials with different retention and immobilization capacities, determined by batch sorption experiments, was investigated. The transport of Na-montmorillonite colloids and well-defined negatively charged latex microspheres of 50, 100, and 200 nm diameter were studied in either columns containing quartz or quartz mixed with biotite. The ionic strength in the solution was exclusively 0.001 and pH 6 or 8.5. The flow rates used were 0.002, 0.03, and 0.6 mL min-1. Sorption of the colloids on the model fracture

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)

Pharmacology of colloids and crystalloids.

Science.gov (United States)

Griffel, M I; Kaufman, B S

1992-04-01

We have attempted to review body fluid distribution by compartments so that the reader understands the physiology of ICF and ECF, and the relationship between interstitial and intravascular fluids. Crystalloids such as NS and RL are distributed to the ECF, whereas colloids primarily remain intravascular for longer periods. Although effective, crystalloids tend to require larger volumes for infusion, and edema remains a problem. Colloids as a group are extremely effective volume expanders, but none is ideal. Albumin, hetastarch, dextran, and the less commonly used colloids each have significant toxicities that must be considered when using them. Intelligent choices can be made to optimize use of these fluids.

Anomalous columnar order of charged colloidal platelets

Science.gov (United States)

Morales-Anda, L.; Wensink, H. H.; Galindo, A.; Gil-Villegas, A.

2012-01-01

Monte Carlo computer simulations are carried out for a model system of like-charged colloidal platelets in the isothermal-isobaric ensemble (NpT). The aim is to elucidate the role of electrostatic interactions on the structure of synthetic clay systems at high particle densities. Short-range repulsions between particles are described by a suitable hard-core model representing a discotic particle. This potential is supplemented with an electrostatic potential based on a Yukawa model for the screened Coulombic potential between infinitely thin disklike macro-ions. The particle aspect-ratio and electrostatic parameters were chosen to mimic an aqueous dispersion of thin, like-charged, rigid colloidal platelets at finite salt concentration. An examination of the fluid phase diagram reveals a marked shift in the isotropic-nematic transition compared to the hard cut-sphere reference system. Several statistical functions, such as the pair correlation function for the center-of-mass coordinates and structure factor, are obtained to characterize the structural organization of the platelets phases. At low salinity and high osmotic pressure we observe anomalous hexagonal columnar structures characterized by interpenetrating columns with a typical intercolumnar distance corresponding to about half of that of a regular columnar phase. Increasing the ionic strength leads to the formation of glassy, disordered structures consisting of compact clusters of platelets stacked into finite-sized columns. These so-called "nematic columnar" structures have been recently observed in systems of charge-stabilized gibbsite platelets. Our findings are corroborated by an analysis of the static structure factor from a simple density functional theory.

The radiation chemistry of colloids

International Nuclear Information System (INIS)

Sellers, R.M.

1976-08-01

One of the most important problems associated with water cooled reactors is the accumulation on the pipework of radio-active deposits. These are formed from corrosion products which become activated during their passage through the reactor core. The first step of the activation process involves the deposition of the corrosion products, which are present as either colloidal or particulate matter, onto surfaces in the reactor core, i.e. within the radiation zone. A review of the literature on the effect of radiation on colloids is presented. Particular emphasis is given to the dependence of colloidal parameters such as particle size, turbidity and electrophoretic mobility on radiation dose. Most of the data available is of a qualitative nature only. Evidence is presented that colloids of iron are affected (in some cases precipitated) by radiation, and it is suggested that this process plays a part in the deposition of corrosion products in nuclear reactor cores. The bulk of the information available can be rationalized in terms of the radiation chemistry of aqueous solutions, and the interaction of the radicals produced with the atoms or molecules at the surface of the colloidal particles. This approach is very successful in explaining the variation of the mean particle size of monodisperse sulphur hydrosols with dose, for which quantitative experimental data are available. (author)

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.

Colloidal quantum dot photovoltaics: The effect of polydispersity

KAUST Repository

Zhitomirsky, David

2012-02-08

The size-effect tunability of colloidal quantum dots enables facile engineering of the bandgap at the time of nanoparticle synthesis. The dependence of effective bandgap on nanoparticle size also presents a challenge if the size dispersion, hence bandgap variability, is not well-controlled within a given quantum dot solid. The impact of this polydispersity is well-studied in luminescent devices as well as in unipolar electronic transport; however, the requirements on monodispersity have yet to be quantified in photovoltaics. Here we carry out a series of combined experimental and model-based studies aimed at clarifying, and quantifying, the importance of quantum dot monodispersity in photovoltaics. We successfully predict, using a simple model, the dependence of both open-circuit voltage and photoluminescence behavior on the density of small-bandgap (large-diameter) quantum dot inclusions. The model requires inclusion of trap states to explain the experimental data quantitatively. We then explore using this same experimentally tested model the implications of a broadened quantum dot population on device performance. We report that present-day colloidal quantum dot photovoltaic devices with typical inhomogeneous linewidths of 100-150 meV are dominated by surface traps, and it is for this reason that they see marginal benefit from reduction in polydispersity. Upon eliminating surface traps, achieving inhomogeneous broadening of 50 meV or less will lead to device performance that sees very little deleterious impact from polydispersity. © 2012 American Chemical Society.

Melanocortin systems on pigment dispersion in fish chromatophores.

Science.gov (United States)

Kobayashi, Yuki; Mizusawa, Kanta; Saito, Yumiko; Takahashi, Akiyoshi

2012-01-01

α-Melanocyte-stimulating hormone (α-MSH) is responsible for pigment dispersion in the chromatophores of fish and other tetrapods such as amphibians and reptiles. Recently, we discovered that α-MSH did not always stimulate pigment dispersion because this hormonal peptide exerted no effects on the melanophores of flounders. We assumed that the reduction of α-MSH activity was related to the co-expression of different α-MSH receptor subtypes - termed melanocortin receptors (MCR) - a member of G-protein-coupled receptors (GPCR) - based on several reports demonstrating that GPCR forms heterodimers with various properties that are distinct from those of the corresponding monomers. In this review, we summarize the relationships between the pigment-dispersing activity of α-MSH-related peptides, molecular forms of α-MSH-related peptides, and mcr subtypes expressed in fish chromatophores.

Structural properties of dendrimer-colloid mixtures

International Nuclear Information System (INIS)

Lenz, Dominic A; Blaak, Ronald; Likos, Christos N

2012-01-01

We consider binary mixtures of colloidal particles and amphiphilic dendrimers of the second generation by means of Monte Carlo simulations. By using the effective interactions between monomer-resolved dendrimers and colloids, we compare the results of simulations of mixtures stemming from a full monomer-resolved description with the effective two-component description at different densities, composition ratios, colloid diameters and interaction strengths. Additionally, we map the two-component system onto an effective one-component model for the colloids in the presence of the dendrimers. Simulations based on the resulting depletion potentials allow us to extend the comparison to yet another level of coarse graining and to examine under which conditions this two-step approach is valid. In addition, a preliminary outlook into the phase behavior of this system is given. (paper)

Influences on physicians' choices of intravenous colloids.

Science.gov (United States)

Miletin, Michael S; Stewart, Thomas E; Norton, Peter G

2002-07-01

Controversy over the optimal intravenous fluid for volume resuscitation continues unabated. Our objectives were to characterize the demographics of physicians who prescribe intravenous colloids and determine factors that enter into their decision to choose a colloid. Questionnaire with 61 items. Ten percent ( n = 364) of frequent intravenous fluid prescribers in the province of Ontario, Canada. The response rate was 74%. Colloid use in the past year was reported by 79% of the responding physicians. Important reasons for choosing a colloid included blood loss and manipulation of oncotic pressure. Physicians tended to prefer either albumin or pentastarch, but no important reasons were found for choosing between the two. Albumin with or without crystalloid was preferred in 5/13 scenarios by more than 50% of the respondents, whereas pentastarch was not favored by more than 50% of respondents in any scenario. Physicians practising in critical care areas and teaching hospitals generally preferred pentastarch to albumin. Physicians reporting pentastarch as representing greater than 90% of total colloid use were more likely to have been visited by a drug detailer for pentastarch than those who used less synthetic colloid (54 vs 22%, p distribution. Although albumin appeared to be preferred in more clinical niches, most physicians did not state reasons for choosing between products. Marketing, specialty, location of practice and clinical scenario appear to play significant roles in the utilization of colloid products.

Characterization of magnetic colloids by means of magnetooptics

OpenAIRE

Baraban, Larysa; Erbe, Artur; Leiderer, Paul

2007-01-01

A new, efficient method for the characterization of magnetic colloids based on the Faraday effect is proposed. According to the main principles of this technique, it is possible to detect the stray magnetic field of the colloidal particles induced inside the magnetooptical layer. The magnetic properties of individual particles can be determined providing measurements in a wide range of magnetic fields. The magnetization curves of capped colloids and paramagnetic colloids were measured by mean...

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

A Molecular Dynamics Study of Single-Walled Carbon Nanotubes (SWCNTs) Dispersed in Bile Salt Surfactants

Science.gov (United States)

Phelan, Frederick, Jr.; Sun, Huai

2014-03-01

Single-walled carbon nanotubes (SWNCTs) are materials with structural, electronic and optical properties that make them attractive for a myriad of advanced technology applications. A practical barrier to their use is that SWCNT synthesis techniques produce heterogeneous mixtures of varying lengths and chirality, whereas applications generally require tubes with narrow size distributions and individual type. Most separation techniques currently in use to obtain monodisperse tube fractions rely on dispersion of these materials in aqueous solution using surfactants. The dispersion process results in a mixture of colloidal structures in which individual tubes are dispersed and contained in a surfactant shell. Understanding the structure and properties of the SWCNT-surfactant complex at the molecular level, and how this is affected by chirality, is key to understanding and improving separations processes. In this study, we use molecular dynamics (MD) simulations to study the structure and properties of SWCNT-surfactant colloidal complexes. We tested a number of methods and protocols in order to build an accurate model for simulating SWCNT systems for a variety of bile salt surfactants as well as anionic co-surfactants, components that are widely used and important in experimental separation studies at NIST. The custom force field parameters used here will be stored in WebFF, a Web-hosted smart force-field repository for polymeric and organic materials being developed at NIST for the Materials Genome Initiative.

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

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

Science.gov (United States)

Uskoković, Vuk

2013-10-01

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

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

Feasibility of the development of reference materials for the detection of Ag nanoparticles in food: neat dispersions and spiked chicken meat

NARCIS (Netherlands)

Grombe, R.; Allmaier, G.; Charoud-Got, J.; Dudkiewicz, A.; Emteborg, H.; Hofmann, T.; Huusfeldt-Larsen, E.; Lehner, A.; Llinas, M.; Loeschner, K.; Molhave, K.; Peters, R.J.B.; Seghers, J.; Solans, C.; Kammer, van den F.; Wagner, S.; Weigel, S.; Linsinger, T.P.J.

2015-01-01

The feasibility of producing colloidal silver nanoparticle reference materials and silver nanoparticle spiked reference matrix materials was investigated. Two concentrations of PVP-coated silver nanoparticle dispersions were evaluated and used to spike chicken meat, with the aim of producing a set

Optical detection of magnetic nanoparticles in colloidal suspensions

Energy Technology Data Exchange (ETDEWEB)

Gimenez, Alejandro J.; Ramirez-Wong, Diana G.; Favela-Camacho, Sarai E. [Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional Unidad Querétaro, Querétaro, México (Mexico); Sanchez, Isaac C. [Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712 (United States); Yáñez-Limón, J.M.; Luna-Bárcenas, Gabriel [Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional Unidad Querétaro, Querétaro, México (Mexico)

2016-03-15

This study reports the change of light transmittance and light scattering dispersion by colloidal suspensions of magnetic nanoparticles. Optical changes were observed during the application of transversal magnetic fields to magnetic nanoparticles and nanowires at concentrations spanning from 20 µg/mL to 2 ng/mL. Results show that light scattering modulation is a simple, fast and inexpensive method for detection of magnetic nanoparticles at low concentrations. Frequency and time response of the optical modulation strongly depends on the geometry of the particles. In this regard, light transmittance and scattering measurements may prove useful in characterizing the morphology of suspended nanoparticles. - Highlights: • A simple route to characterize magnetic nanowire suspension is proposed. • Studied concentration as low as 2 ng/mL compares with more complex techniques. • Transmission and scattering modes allow full characterization of nanoparticles.

Phosphate binding by natural iron-rich colloids in streams

NARCIS (Netherlands)

Baken, S.; Moens, C.; Griffioen, J.J.; Smolders, E.

2016-01-01

Phosphorus (P) in natural waters may be bound to iron (Fe) bearing colloids. However, the natural variation in composition and P binding strength of these colloids remain unclear. We related the composition of "coarse colloids" (colloids in the 0.1-1.2 μm size range) in 47 Belgian streams to the

Microbial effects on colloidal agglomeration

International Nuclear Information System (INIS)

Hersman, L.

1995-11-01

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

Behavior of colloids in radionuclide migration in deep geologic formation

International Nuclear Information System (INIS)

Kanno, Takuji

1994-01-01

In case high level waste is isolated in deep strata, it is important to elucidate the behavior of movement that radionuclides take in the strata. Recently, it has been recognized that the participation of colloids is very important, and it has been studied actively. In this study, as to the mechanism of the adsorption of colloids to geological media or buffers, analysis was carried out for a number of systems, and it was clarified in what case they are caught or they move without being caught. Also it is considered what research is necessary hereafter. First, the kinds of colloids are shown. As the properties of colloids that control the movement of colloids in groundwater in deep strata, the surface potential, shape, size and so on of colloids are conceivable. These properties are briefly discussed. As the interaction of colloids and geological media, the interaction by electrostatic attraction, the fast and slow movement of colloids through rock crevices, and the filtration of colloids in buffers and porous media are described. The experimental results on the movement of colloids are reported. (K.I.)

Does mental exertion alter maximal muscle activation?

Directory of Open Access Journals (Sweden)

Vianney eRozand

2014-09-01

Full Text Available Mental exertion is known to impair endurance performance, but its effects on neuromuscular function remain unclear. The purpose of this study was to test the hypothesis that mental exertion reduces torque and muscle activation during intermittent maximal voluntary contractions of the knee extensors. Ten subjects performed in a randomized order three separate mental exertion conditions lasting 27 minutes each: i high mental exertion (incongruent Stroop task, ii moderate mental exertion (congruent Stroop task, iii low mental exertion (watching a movie. In each condition, mental exertion was combined with ten intermittent maximal voluntary contractions of the knee extensor muscles (one maximal voluntary contraction every 3 minutes. Neuromuscular function was assessed using electrical nerve stimulation. Maximal voluntary torque, maximal muscle activation and other neuromuscular parameters were similar across mental exertion conditions and did not change over time. These findings suggest that mental exertion does not affect neuromuscular function during intermittent maximal voluntary contractions of the knee extensors.

Synthesis and characterization of ultrafine well-dispersed magnetic nanoparticles

International Nuclear Information System (INIS)

Liu, Z.L.; Wang, H.B.; Lu, Q.H.; Du, G.H.; Peng, L.; Du, Y.Q.; Zhang, S.M.; Yao, K.L.

2004-01-01

Ultrafine well-dispersed magnetic nanoparticles were directly prepared in aqueous solution using controlled coprecipitation method. The structure, size, size distributions and magnetic properties of the magnetic nanoparticles, characterized by TEM, XRD and VSM, indicated the formation of single domain nanoparticles with average size smaller than 5 nm. The magnetic nanoparticles show superparamagnetism and a lower saturation magnetization is found as a consequence of smaller particle size. The relevant conditions for obtaining these magnetic colloids are discussed and the so-prepared magnetic nanoparticles are stable in a wide pH range

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

Suspensions of colloidal particles and aggregates

CERN Document Server

Babick, Frank

2016-01-01

This book addresses the properties of particles in colloidal suspensions. It has a focus on particle aggregates and the dependency of their physical behaviour on morphological parameters. For this purpose, relevant theories and methodological tools are reviewed and applied to selected examples. The book is divided into four main chapters. The first of them introduces important measurement techniques for the determination of particle size and interfacial properties in colloidal suspensions. A further chapter is devoted to the physico-chemical properties of colloidal particles—highlighting the interfacial phenomena and the corresponding interactions between particles. The book’s central chapter examines the structure-property relations of colloidal aggregates. This comprises concepts to quantify size and structure of aggregates, models and numerical tools for calculating the (light) scattering and hydrodynamic properties of aggregates, and a discussion on van-der-Waals and double layer interactions between ...

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

Silica colloids and their effect on radionuclide sorption. A literature review

International Nuclear Information System (INIS)

Hoelttae, P.; Hakanen, M.

2008-05-01

Silica sol, commercial colloidal silica manufactured by Eka Chemicals in Bohus, Sweden is a promising inorganic grout material for sealing small fractures in low permeable rock. This literature review collects information about the use of silica sol as an injection grout material, the properties of inorganic, especially silica colloids, colloid contents in granitic groundwater conditions, essential characterization methods and colloid-mediated transport of radionuclides. Objective was to evaluate the release and mobility of silica sol colloids, the effect of the groundwater conditions, the amount of colloids compared with natural colloids in Olkiluoto conditions, radionuclide sorption on colloids and their contribution to radionuclide transport. Silica sol seems to be a feasible material to seal fractures with an aperture as small as 10 μm in low permeable rock. The silica sol gel is sufficiently stable to limit to water ingress during the operational phase, the requirement that the pH should be below 11 is fulfilled and the compatibility with Engineered Barrier System (EBS) materials is expected to be good. No significant influence on the bentonite properties caused by the silica sol is expected when calcium chloride is used as an accelerator but the influence of sodium chloride has not been examined. No significant release of colloids is expected under prevailing groundwater conditions. The long-term (100 y) stability of silica sol gel has not yet been clearly demonstrated and a long-term release of silica colloids cannot be excluded. The question is the amount of colloids, how mobile they are and the influence of possible glacial melt waters. The bentonite buffer used in the EBS system is assumed to be a potential source of colloids. In a study in Olkiluoto, bentonite colloids were found only in low salinity groundwater. In general, low salinity water (total dissolved solids -1 ) favours colloid stability and bentonite colloids can remain stable over long

Determination of radiochemical purity and pharmacokinetic parameters of sup(99m)Tc-sulphur colloid and sup(99m)Tc-tin colloid

International Nuclear Information System (INIS)

Jovanovic, V.; Konstantinovska, D.; Milivojevic, K.; Bzenic, J.

1981-01-01

Labelling yield and radiochemical purity, higher than 95%, of sup(99m)Tc-colloid preparations were determined by using the paper chromatography method. Less than 3% of labelled citric acid, added to the preparation as a buffer solution, has been found in sup(99m)Tc-sulphur colloid. High radiochemical purity and optimum size of colloid particles has also been proved by biodistribution studies on experimental animals. The analysis performed has shown that more than 50% of sup(99m)Tc-colloid preparations excreted by urine is sup(99m)TcO - , the remaining past 50% being protein bound sup(99m)Tc. Biological half-time of excretion of the fast phase is the same for both preparations, i.e. 10 min, while for the slow component it is 120 min in sup(99m)Tc-S-colloid and 160 min in sup(99m)Tc-Sn colloid. (orig.) [de

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.

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

Exertional dyspnoea in obesity

Directory of Open Access Journals (Sweden)

Vipa Bernhardt

2016-12-01

Full Text Available The purpose of cardiopulmonary exercise testing (CPET in the obese person, as in any cardiopulmonary exercise test, is to determine the patient's exercise tolerance, and to help identify and/or distinguish between the various physiological factors that could contribute to exercise intolerance. Unexplained dyspnoea on exertion is a common reason for CPET, but it is an extremely complex symptom to explain. Sometimes obesity is the simple answer by elimination of other possibilities. Thus, distinguishing among multiple clinical causes for exertional dyspnoea depends on the ability to eliminate possibilities while recognising response patterns that are unique to the obese patient. This includes the otherwise healthy obese patient, as well as the obese patient with potentially multiple cardiopulmonary limitations. Despite obvious limitations in lung function, metabolic disease and/or cardiovascular dysfunction, obesity may be the most likely reason for exertional dyspnoea. In this article, we will review the more common cardiopulmonary responses to exercise in the otherwise healthy obese adult with special emphasis on dyspnoea on exertion.

Analysis report for WIPP colloid model constraints and performance assessment parameters

Energy Technology Data Exchange (ETDEWEB)

Mariner, Paul E.; Sassani, David Carl

2014-03-01

An analysis of the Waste Isolation Pilot Plant (WIPP) colloid model constraints and parameter values was performed. The focus of this work was primarily on intrinsic colloids, mineral fragment colloids, and humic substance colloids, with a lesser focus on microbial colloids. Comments by the US Environmental Protection Agency (EPA) concerning intrinsic Th(IV) colloids and Mg-Cl-OH mineral fragment colloids were addressed in detail, assumptions and data used to constrain colloid model calculations were evaluated, and inconsistencies between data and model parameter values were identified. This work resulted in a list of specific conclusions regarding model integrity, model conservatism, and opportunities for improvement related to each of the four colloid types included in the WIPP performance assessment.

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)

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

Evaluation of the liver scintigraphy with /sup 99m/Tc-Sn-colloid. II. C Clinical studies by comparison with /sup 198/Au-colloid

Energy Technology Data Exchange (ETDEWEB)

Kimura, K; Nishimura, T; Takeda, H; Furukawa, T [Osaka Univ. (Japan). Faculty of Medicine; Kajiya, Fumihiko

1975-08-01

Clinical significance of the liver scintigraphy with sup(99m)Tc-Sn-colloid was evaluated in comparison with those with /sup 198/Au-colloid. The liver scintigrams with sup(99m)Tc-Sn-colloid and /sup 198/Au-colloid were done in 36 cases of various hepatic diseases and RI accumulation curves in the liver and the spleen, and the blood disapearance curves were also obtained. The conclusions were as follows. The liver scintigrams with sup(99m)Tc-Sn-colloid proved to be more sensitive in the detection of tumors, especially, in the lower margin, left lobe and superficial layers of the liver than those with /sup 198/Au-colloid. In all cases, including normal and cirrhotic subjects, visualizations of the spleen were seen on the scintigrams with sup(99m)Tc-Sn-colloid. In diffuse hepatic diseases, comparing both radiopharmaceuticals, the splenic accumulations were studied qualitatively and quantitatively. As a result, the ratio (spleen/liver) was thought to be useful for the differentiation of diffuse hepatic diseases concerned with splenic function and/or size. It was also shown that sup(99m)Tc-Sn-colloid was useful as a spleen scanning agent. The Tl/2 in the liver accumulation curves with sup(99m)Tc-Sn-colloid were not as clearly differentiated in the various hepatic diseases as those with /sup 198/Au-colloid where those indexes were useful in the evaluation of liver functions.

Rheological Characteristics of 2D Titanium Carbide (MXene) Dispersions: A Guide for Processing MXenes.

Science.gov (United States)

Akuzum, Bilen; Maleski, Kathleen; Anasori, Babak; Lelyukh, Pavel; Alvarez, Nicolas Javier; Kumbur, E Caglan; Gogotsi, Yury

2018-03-27

Understanding the rheological properties of two-dimensional (2D) materials in suspension is critical for the development of various solution processing and manufacturing techniques. 2D carbides and nitrides (MXenes) constitute one of the largest families of 2D materials with >20 synthesized compositions and applications already ranging from energy storage to medicine to optoelectronics. However, in spite of a report on clay-like behavior, not much is known about their rheological response. In this study, rheological behavior of single- and multilayer Ti 3 C 2 T x in aqueous dispersions was investigated. Viscous and viscoelastic properties of MXene dispersions were studied over a variety of concentrations from colloidal dispersions to high loading slurries, showing that a multilayer MXene suspension with up to 70 wt % can exhibit flowability. Processing guidelines for the fabrication of MXene films, coatings, and fibers have been established based on the rheological properties. Surprisingly, high viscosity was observed at very low concentrations for solutions of single-layer MXene flakes. Single-layer colloidal solutions were found to exhibit partial elasticity even at the lowest tested concentrations (<0.20 mg/mL) due to the presence of strong surface charge and excellent hydrophilicity of MXene, making them amenable to fabrication at dilute concentrations. Overall, the findings of this study provide fundamental insights into the rheological response of this quickly growing 2D family of materials in aqueous environments as well as offer guidelines for processing of MXenes.

Investigation on the Stability of Aluminosilicate Colloids by Various Analytical Tools

Energy Technology Data Exchange (ETDEWEB)

Putri, Kirana Y.; Lee, D. H.; Yun, J. I. [Korea Advanced Institute of Science and Technology, Daejeon (Korea, Republic of)

2010-05-15

Colloids are ubiquitous in natural aquatic systems. Aquatic colloids may play a significant carrier role for radionuclide migration in aquifer systems. Being omnipresent in natural aquatic systems, aluminosilicate colloids are considered as a kernel for various aquatic colloids. Characterization of aluminosilicate colloids formed under various geochemical conditions is of importance to understand their chemical behavior in natural aquatic systems. In this work, a preliminary study on the formation of aluminosilicate colloids with a help of colorimetry and other colloid detection techniques is presented

Component-Customizable Porous Rare-Earth-Based Colloidal Spheres towards Highly Effective Catalysts and Bioimaging Applications.

Science.gov (United States)

Li, Cheng Chao; Rui, Xianhong; Wei, Weifeng; Chen, Libao; Yu, Yan

2017-11-16

Multicomponent porous colloidal spheres are of interest because they not only show a combination of the properties associated with all different components, but also usually present synergy effects. However, a combination of different components in a single porous sphere is still greatly challenged due to the different precipitation behaviors of each component. In this work, we have developed a general synthetic route to prepare several categories of porous monodisperse rare-earth (RE)-based colloidal spheres with customizable elemental compositions and a uniform element distribution. The two-step synthetic strategy is based on the integration of coordination chemistry precipitation of RE ions and a subsequent ion-exchange process, which steers clear of obstacles, such as differences in solubility product constant, that are to be found in traditional co-precipitation methods. Our approach provides a new mixing mechanism to realize homogeneous distribution of each element within the porous spheres. An array of binary, ternary, and even senary RE colloidal porous spheres with diameters of 500 nm to 700 nm has been successfully synthesized. Taking advantage of their good dispersibility, porosity, and customizable components, these porous RE oxide spheres show excellent catalytic activity for the reduction of 4-nitrophenol, and promising application in single-phase multifunctional bioprobes. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entropy favours open colloidal lattices

Science.gov (United States)

Mao, Xiaoming; Chen, Qian; Granick, Steve

2013-03-01

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

Patterned Colloidal Photonic Crystals.

Science.gov (United States)

Hou, Jue; Li, Mingzhu; Song, Yanlin

2018-03-01

Colloidal photonic crystals (PCs) have been well developed because they are easy to prepare, cost-effective, and versatile with regards to modification and functionalization. Patterned colloidal PCs contribute a novel approach to constructing high-performance PC devices with unique structures and specific functions. In this review, an overview of the strategies for fabricating patterned colloidal PCs, including patterned substrate-induced assembly, inkjet printing, and selective immobilization and modification, is presented. The advantages of patterned PC devices are also discussed in detail, for example, improved detection sensitivity and response speed of the sensors, control over the flow direction and wicking rate of microfluidic channels, recognition of cross-reactive molecules through an array-patterned microchip, fabrication of display devices with tunable patterns, well-arranged RGB units, and wide viewing-angles, and the ability to construct anti-counterfeiting devices with different security strategies. Finally, the perspective of future developments and challenges is presented. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Influence of Protamine Functionalization on the Colloidal Stability of 1D and 2D Titanium Oxide Nanostructures.

Science.gov (United States)

Rouster, Paul; Pavlovic, Marko; Horváth, Endre; Forró, László; Dey, Sandwip K; Szilagyi, Istvan

2017-09-26

The colloidal stability of titanium oxide nanosheets (TNS) and nanowires (TiONW) was studied in the presence of protamine (natural polyelectrolyte) in aqueous dispersions, where the nanostructures possessed negative net charge, and the protamine was positively charged. Regardless of their shape, similar charging and aggregation behaviors were observed for both TNS and TiONW. Electrophoretic experiments performed at different protamine loadings revealed that the adsorption of protamine led to charge neutralization and charge inversion depending on the polyelectrolyte dose applied. Light scattering measurements indicated unstable dispersions once the surface charge was close to zero or slow aggregation below and above the charge neutralization point with negatively or positively charged nanostructures, respectively. These stability regimes were confirmed by the electron microscopy images taken at different polyelectrolyte loadings. The protamine dose and salt-dependent colloidal stability confirmed the presence of DLVO-type interparticle forces, and no experimental evidence was found for additional interactions (e.g., patch-charge, hydrophobic, or steric forces), which are usually present in similar polyelectrolyte-particle systems. These findings indicate that the polyelectrolyte adsorbs on the TNS and TiONW surfaces in a flat and extended conformation giving rise to the absence of surface heterogeneities. Therefore, protamine is an excellent biocompatible candidate to form smooth surfaces, for instance in multilayers composed of polyelectrolytes and particles to be used in biomedical applications.

The influence of colloids on the migration of radionuclides

International Nuclear Information System (INIS)

Seher, Holger

2011-01-01

For a concept of deep geological disposal of high level nuclear waste, the repository will be designed as a multiple-barrier system including bentonite as the buffer/backfill material and the host rock formation as the geological barrier. The engineered barrier (compacted bentonite) will be in contact with the host rock formation (e.g. granite). Consequently the bentonite will be saturated over time with formation groundwater, which will induce swelling and gel formation of the bentonite. At the gel-groundwater boundary, colloid detachment might be a possible colloid source and therefore might enhance the mobility of strong sorbing actinides. This work will focus on three aspects of colloidal transport: (a) Colloid stability in the mixing zone between granite groundwater and bentonite pore water, including its description with an extended DLVO model. (b) Colloid generation and erosion of the bentonite at the interface between compacted bentonite and granitic groundwater, as well as formation of new colloids in the mixing zone between the bentonite porewater and the granitic groundwater. (c) Colloid transport and the interaction of U, Th, Hf, Tb, Eu and Cm with bentonite colloids and fracture filling material, as well as their mobility in a natural fracture.

Melanocortin systems on pigment dispersion in fish chromatophores

Directory of Open Access Journals (Sweden)

Yuki eKobayashi

2012-02-01

Full Text Available Alpha-Melanocyte-stimulating hormone (alpha-MSH is responsible for pigment dispersion in the chromatophores of fish and other tetrapods such as amphibians and reptiles. Recently, we discovered that alpha-MSH did not always stimulate pigment dispersion because this hormonal peptide exerted no effects on the melanophores of flounders. We assumed that the reduction of alpha-MSH activity was related to the co-expression of different alpha-MSH receptor subtypes—termed melanocortin receptors (MCR—a member of G-protein-coupled receptors (GPCR—based on several reports demonstrating that GPCR forms heterodimers with various properties that are distinct from those of the corresponding monomers. In this review, we summarize the relationships between the pigment-dispersing activity of alpha-MSH-related peptides, molecular forms of alpha-MSH-related peptides, and Mcr subtypes expressed in fish chromatophores.

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

Science.gov (United States)

Uskoković, Vuk

2013-01-01

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

Hydrodynamic interactions in active colloidal crystal microrheology

OpenAIRE

Weeber, R; Harting, JDR Jens

2012-01-01

In dense colloids it is commonly assumed that hydrodynamic interactions do not play a role. However, a found theoretical quantification is often missing. We present computer simulations that are motivated by experiments where a large colloidal particle is dragged through a colloidal crystal. To qualify the influence of long-ranged hydrodynamics, we model the setup by conventional Langevin dynamics simulations and by an improved scheme with limited hydrodynamic interactions. This scheme signif...

Rheological behavior of high-concentration sodium caseinate dispersions.

Science.gov (United States)

Loveday, Simon M; Rao, M Anandha; Creamer, Lawrence K; Singh, Harjinder

2010-03-01

Apparent viscosity and frequency sweep (G', G'') data for sodium caseinate dispersions with concentrations of approximately 18% to 40% w/w were obtained at 20 degrees C; colloidal glass behavior was exhibited by dispersions with concentration >or=23% w/w. The high concentrations were obtained by mixing frozen powdered buffer with sodium caseinate in boiling liquid nitrogen, and allowing the mixtures to thaw and hydrate at 4 degrees C. The low-temperature G'-G'' crossover seen in temperature scans between 60 and 5 degrees C was thought to indicate gelation. Temperature scans from 5 to 90 degrees C revealed gradual decrease in G' followed by plateau values. In contrast, G'' decreased gradually and did not reach plateau values. Increase in hydrophobicity of the sodium caseinate or a decrease in the effective volume fraction of its aggregates may have contributed to these phenomena. The gelation and end of softening temperatures of the dispersions increased with the concentration of sodium caseinate. From an Eldridge-Ferry plot, the enthalpy of softening was estimated to be 29.6 kJ mol(-1). The results of this study should be useful for creating new products with high concentrations of sodium caseinate.

Better Resolved Low Frequency Dispersions by the Apt Use of Kramers-Kronig Relations, Differential Operators, and All-In-1 Modeling

NARCIS (Netherlands)

van Turnhout, J.

2016-01-01

The dielectric spectra of colloidal systems often contain a typical low frequency dispersion, which usually remains unnoticed, because of the presence of strong conduction losses. The KK relations offer a means for converting ε′ into ε″ data. This allows us to calculate conduction free ε″ spectra in

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.

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

USE OF WOOD DERIVATIVES AS DOPING / DISPERSING AGENTS IN THE PREPARATION OF POLYPYRROLE AQUEOUS DISPERSIONS

Directory of Open Access Journals (Sweden)

Claudia Sasso

2008-11-01

Full Text Available Polystyrene sulfonic acid (PSS, lignosulfonic acid (LS sodium salts, and carboxymethylcellulose (CMC were used as doping/dispersing agents in the chemical polymerization of polypyrrole (Ppy. Conductivity measure-ments performed on dry Ppy pellets showed a sharp increase in conductivity when adding the anionic polymers to the polymerization liquor. For a polyanion/pyrrole weight ratio ranging between 0.1 and 0.6, the highest conductivity was given by PpyCMC (82 S/m and PpyPSS (80 S/m, followed by PpyLS (6 S/m. On the other hand, for a polyanion/pyrrole ratio higher than 0.6, the conductivity of PpyPSS systems sharply decreased, and for polyanion/pyrrole ratios higher than 1, the highest conductivity was given by PpyCMC (~10 S/m, followed by PpyLS (~7 S/m and PpyPSS (~5 S/m. Zeta-potential measurements showed that the surface charge of Ppy was strongly affected by the polyanion type and amount. Cationic Ppy particles were obtained in the presence of the two polymers bearing strongly acidic moieties (PSS and LS. Anionic PpyPSS colloids were obtained at the highest PSS/Py ratio, after the degradation of the conducting properties. When using a weakly acidic dopant (CMC, PpyCMC colloids had a negative charge for all of the tested conditions.

Bonding assembled colloids without loss of colloidal stability

NARCIS (Netherlands)

Vutukuri, H.R.; Stiefelhagen, J.C.P.; Vissers, T; Imhof, A.; van Blaaderen, A.

2012-01-01

In recent years the diversity of self-assembled colloidal structures has strongly increased, as it is fueled by a wide range of applications in materials science and also in soft condensed-matter physics.[1–4] Some potential applications include photonic bandgap (PBG) crystals, materials for

Colloidal Fe-doped ZnO nanocrystals: Facile low temperature synthesis, characterization and properties

Energy Technology Data Exchange (ETDEWEB)

Singhal, A. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)], E-mail: ansing@barc.gov.in; Achary, S.N.; Tyagi, A.K. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Manna, P.K.; Yusuf, S.M. [Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

2008-09-25

Colloidal Fe-doped ZnO nanocrystals, Zn{sub 1-x}Fe{sub x}O (x = 0.00, 0.05, 0.07 and 0.1) have been prepared by thermal decomposition of metal precursors at 200 deg. C with hexadecylamine (HDA) as solvent and surfactant. The nanocrystals so prepared can be easily dispersed in non-polar solvents like chloroform and toluene. The nanocrystals have been structurally characterized using X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), energy dispersive X-ray analysis (EDX) and X-ray photoelectron spectroscopy (XPS). Magnetization measurements on a representative sample, Zn{sub 0.95}Fe{sub 0.05}O using a vibrating sample magnetometer (VSM) reveal that the nanocrystals exhibit a weak ferromagnetic behavior at 300 K. This observation is further confirmed by the electron paramagnetic resonance spectrum of Zn{sub 0.95}Fe{sub 0.05}O nanocrystals, which shows a distinct ferromagnetic resonance signal at room temperature.

Seed predators exert selection on the subindividual variation of seed size.

Science.gov (United States)

Sobral, M; Guitián, J; Guitián, P; Larrinaga, A R

2014-07-01

Subindividual variation among repeated organs in plants constitutes an overlooked level of variation in phenotypic selection studies, despite being a major component of phenotypic variation. Animals that interact with plants could be selective agents on subindividual variation. This study examines selective pressures exerted during post-dispersal seed predation and germination on the subindividual variation of seed size in hawthorn (Crataegus monogyna). With a seed offering experiment and a germination test, we estimated phenotypic selection differentials for average and subindividual variation of seed size due to seed predation and germination. Seed size affects germination, growth rate and the probability of an individual seed of escaping predation. Longer seeds showed higher germination rates, but this did not result in significant selection on phenotypes of the maternal trees. On the other hand, seed predators avoided wider seeds, and by doing so exerted phenotypic selection on adult average and subindividual variation of seed size. The detected selection on subindividual variation suggests that the levels of phenotypic variation within individual plants may be, at least partly, the adaptive consequence of animal-mediated selection. © 2013 German Botanical Society and The Royal Botanical Society of the Netherlands.

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

Colloid cyst in pituitary gland: a case report

International Nuclear Information System (INIS)

Koo, Hee Youn; Lee, Myung Jun; Lee, Chang Joon; Yoo, Jeong Hyun

2001-01-01

Colloid cyst is a congenital lesion which is thought to be derived from the primitive neuro epithelium, and is most frequently located in the anterior half of the third ventricle. Colloid cysts rarely occur in the pituitary gland, and we describe a case of pituitary colloid cyst, including the CT, MRI and pathologic findings

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.

Sodium caseinate stabilized zein colloidal particles.

Science.gov (United States)

Patel, Ashok R; Bouwens, Elisabeth C M; Velikov, Krassimir P

2010-12-08

The present work deals with the preparation and stabilization of zein colloidal particles using sodium caseinate as electrosteric stabilizer. Colloidal particles with well-defined size range (120-150 nm) and negative surface potential (-29 to -47 mV) were obtained using a simple antisolvent precipitation method. Due to the presence of caseinate, the stabilized colloidal particles showed a shift of isoelectric point (IEP) from 6.0 to around pH 5.0 and thus prevent the aggregation of zein near its native IEP (pH 6.2). The particles also showed good stability to varying ionic strength (15 mM-1.5 M NaCl). Furthermore, stabilized particles retained the property of redispersibility after drying. In vitro protein hydrolysis study confirmed that the presence of caseinate did not alter the digestibility of zein. Such colloidal particles could potentially serve as all-natural delivery systems for bioactive molecules in food, pharmaceutical, and agricultural formulations.

Solid colloids with surface-mobile linkers

International Nuclear Information System (INIS)

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

2015-01-01

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

Surface modification and characterization for dispersion stability of inorganic nanometer-scaled particles in liquid media

International Nuclear Information System (INIS)

Kamiya, Hidehiro; Iijima, Motoyuki

2010-01-01

Inorganic nanoparticles are indispensable for science and technology as materials, pigments and cosmetics products. Improving the dispersion stability of nanoparticles in various liquids is essential for those applications. In this review, we discuss why it is difficult to control the stability of nanoparticles in liquids. We also overview the role of surface interaction between nanoparticles in their dispersion and characterization, e.g. by colloid probe atomic force microscopy (CP-AFM). Two types of surface modification concepts, post-synthesis and in situ modification, were investigated in many previous studies. Here, we focus on post-synthesis modification using adsorption of various kinds of polymer dispersants and surfactants on the particle surface, as well as surface chemical reactions of silane coupling agents. We discuss CP-AFM as a technique to analyze the surface interaction between nanoparticles and the effect of surface modification on the nanoparticle dispersion in liquids. (topical review)

Surface modification and characterization for dispersion stability of inorganic nanometer-scaled particles in liquid media

Directory of Open Access Journals (Sweden)

Hidehiro Kamiya and Motoyuki Iijima

2010-01-01

Full Text Available Inorganic nanoparticles are indispensable for science and technology as materials, pigments and cosmetics products. Improving the dispersion stability of nanoparticles in various liquids is essential for those applications. In this review, we discuss why it is difficult to control the stability of nanoparticles in liquids. We also overview the role of surface interaction between nanoparticles in their dispersion and characterization, e.g. by colloid probe atomic force microscopy (CP-AFM. Two types of surface modification concepts, post-synthesis and in situ modification, were investigated in many previous studies. Here, we focus on post-synthesis modification using adsorption of various kinds of polymer dispersants and surfactants on the particle surface, as well as surface chemical reactions of silane coupling agents. We discuss CP-AFM as a technique to analyze the surface interaction between nanoparticles and the effect of surface modification on the nanoparticle dispersion in liquids.

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.)

Exerting Capacity.

Science.gov (United States)

Leger, J Michael; Phillips, Carolyn A

2017-05-01

Patient safety has been at the forefront of nursing research since the release of the Institute of Medicine's report estimating the number of preventable adverse events in hospital settings; yet no research to date has incorporated the perspectives of bedside nurses using classical grounded theory (CGT) methodology. This CGT study explored the perceptions of bedside registered nurses regarding patient safety in adult acute care hospitals. Data analysis used three techniques unique to CGT-the constant comparative method, coding, and memoing-to explore the values, realities, and beliefs of bedside nurses about patient safety. The analysis resulted in a substantive theory, Exerting Capacity, which explained how bedside nurses balance the demands of keeping their patients safe. Exerting Capacity has implications for health care organization leaders, nursing leaders, and bedside nurses; it also has indications for future research into the concept of patient safety.

Monodisperse, submicrometer-scale platinum colloidal spheres with high electrocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Zhang, Lixue; Wang, Liang; Guo, Shaojun; Zhai, Junfeng; Dong, Shaojun; Wang, Erkang [State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, 130022 Jilin, Changchun (China)

2009-02-15

Monodisperse, submicrometer-scale platinum (Pt) colloidal spheres were prepared through a simple direct chemical reduction of p-phenylenediamine (PPD)-chloroplatinic acid (H{sub 2}PtCl{sub 6}) coordination polymer colloids. It was found that the prepared Pt colloids had the similar size and morphology with their coordination polymer precursors, and the prepared Pt colloids with rough surfaces were three-dimensional (3D) structured assemblies of high-density small Pt nanoparticles. The electrochemical experiments confirmed that the prepared Pt colloids possessed a high electrocatalytic activity towards mainly four-electron reduction of dioxygen to water, making the prepared Pt colloids potential candidates for the efficient cathode material in fuel cells. (author)

A differential dielectric spectroscopy setup to measure the electric dipole moment and net charge of colloidal quantum dots.

Science.gov (United States)

Kortschot, R J; Bakelaar, I A; Erné, B H; Kuipers, B W M

2014-03-01

A sensitive dielectric spectroscopy setup is built to measure the response of nanoparticles dispersed in a liquid to an alternating electric field over a frequency range from 10(-2) to 10(7) Hz. The measured complex permittivity spectrum records both the rotational dynamics due to a permanent electric dipole moment and the translational dynamics due to net charges. The setup consists of a half-transparent capacitor connected in a bridge circuit, which is balanced on pure solvent only, using a software-controlled compensating voltage. In this way, the measured signal is dominated by the contributions of the nanoparticles rather than by the solvent. We demonstrate the performance of the setup with measurements on a dispersion of colloidal CdSe quantum dots in the apolar liquid decalin.

Biomolecule-assisted exfoliation and dispersion of graphene and other two-dimensional materials: a review of recent progress and applications.

Science.gov (United States)

Paredes, J I; Villar-Rodil, S

2016-08-25

Direct liquid-phase exfoliation of layered materials by means of ultrasound, shear forces or electrochemical intercalation holds enormous promise as a convenient, cost-effective approach to the mass production of two-dimensional (2D) materials, particularly in the form of colloidal suspensions of high quality and micrometer- and submicrometer-sized flakes. Of special relevance due to environmental and practical reasons is the production of 2D materials in aqueous medium, which generally requires the use of certain additives (surfactants and other types of dispersants) to assist in the exfoliation and colloidal stabilization processes. In this context, biomolecules have received, in recent years, increasing attention as dispersants for 2D materials, as they provide a number of advantages over more conventional, synthetic surfactants. Here, we review research progress in the use of biomolecules as exfoliating and dispersing agents for the production of 2D materials. Although most efforts in this area have focused on graphene, significant advances have also been reported with transition metal dichalcogenides (MoS2, WS2, etc.) or hexagonal boron nitride. Particular emphasis is placed on the specific merits of different types of biomolecules, including proteins and peptides, nucleotides and nucleic acids (RNA, DNA), polysaccharides, plant extracts and bile salts, on their role as efficient colloidal dispersants of 2D materials, as well as on the potential applications that have been explored for such biomolecule-exfoliated materials. These applications are wide-ranging and encompass the fields of biomedicine (photothermal and photodynamic therapy, bioimaging, biosensing, etc.), energy storage (Li- and Na-ion batteries), catalysis (e.g., catalyst supports for the oxygen reduction reaction or electrocatalysts for the hydrogen evolution reaction), or composite materials. As an incipient area of research, a number of knowledge gaps, unresolved issues and novel future

Facile hydrothermal method for synthesizing nitrogen-doped graphene nanoplatelets using aqueous ammonia: dispersion, stability in solvents and thermophysical performances

Science.gov (United States)

Shafiah Shazali, Siti; Amiri, Ahmad; Zubir, Mohd. Nashrul Mohd; Rozali, Shaifulazuar; Zakuan Zabri, Mohd; Sabri, Mohd Faizul Mohd

2018-03-01

A simple and green approach has been developed to synthesize nitrogen-doped graphene nanoplatelets (N-doped GNPs) for mass production with a very high stability in different solvents e.g. water, ethylene glycol, methanol, ethanol, and 1-hexanol. The strategy is based on mild oxidation of GNPs using hydrogen peroxide and doping with nitrogen using hydrothermal process. The modification of N-doped GNPs was demonstrated by FTIR, TGA, XPS, Raman spectroscopy and high resolution-transmission electron microscope (HRTEM). Further study was carried out by using N-doped GNPs as an additive to prepare different colloidal dispersions. Water-based N-doped GNPs, methanol-based N-doped GNPs, ethanol-based N-doped GNPs, ethylene-glycol based N-doped GNPs and 1-hexanol-based N-doped GNPs dispersions at 0.01 wt.% shown great colloidal stabilities, indicating 17%, 29%, 33%, 18%, and 43% sedimentations after a 15-days period, respectively. The thermophysical properties e.g., viscosity and thermal conductivity of water-based N-doped GNP nanofluids were also evaluated for different weight concentrations of 0.100, 0.075, 0.050, and 0.025 wt.%. Through this, it is found that the obtained dispersions have great potential to be used as working fluids for industrial thermal systems.

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

Mobility of radioactive colloidal particles in groundwater

International Nuclear Information System (INIS)

Nuttall, H.E.; Long, R.L.

1993-01-01

Radiocolloids are a major factor in the rapid migration of radioactive waste in groundwater. For at least two Los Alamos National Laboratory (LANL) sites, researchers have shown that groundwater colloidal particles were responsible for the rapid transport of radioactive waste material in groundwater. On an international scale, a review of reported field observations, laboratory column studies, and carefully collected field samples provides compelling evidence that colloidal particles enhance both radioactive and toxic waste migration. The objective of this project is to understand and predict colloid-contaminant migration through fundamental mathematical models, water sampling, and laboratory experiments and use this information to develop an effective and scientifically based colloid immobilization strategy. The article focuses on solving the suspected radiocolloid transport problems at LANL's Mortandad Canyon site. (author) 6 figs., 5 tabs., 18 refs

A general method to coat colloidal particles with titiana

NARCIS (Netherlands)

Demirors, A.F.; van Blaaderen, A.; Imhof, A.

2010-01-01

We describe a general one-pot method for coating colloidal particles with amorphous titania. Various colloidal particles such as silica particles, large silver colloids, gibbsite platelets, and polystyrene spheres were successfully coated with a titania shell. Although there are several ways of

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.

Field-scale colloid migration experiments in a granite fracture

International Nuclear Information System (INIS)

Vilks, P.; Frost, L.H.; Bachinski, D.B.

1997-01-01

An understanding of particle migration in fractured rock, required to assess the potential for colloid-facilitated transport of radionuclides, can best be evaluated when the results of laboratory experiments are demonstrated in the field. Field-scale migration experiments with silica colloids were carried out at AECL's Underground Research Laboratory (URL), located in southern Manitoba, to develop the methodology for large-scale migration experiments and to determine whether colloid transport is possible over distances up to 17 m. In addition, these experiments were designed to evaluate the effects of flow rate and flow path geometry, and to determine whether colloid tracers could be used to provide additional information on subsurface transport to that provided by conservative tracers alone. The colloid migration studies were carried out as part of AECL's Transport Properties in Highly Fractured Rock Experiment, the objective of which was to develop and demonstrate methods for evaluating the solute transport characteristics of zones of highly fractured rock. The experiments were carried out within fracture zone 2 as two-well recirculating, two-well non-recirculating, and convergent flow tests, using injection rates of 5 and 101 min -1 . Silica colloids with a 20 nm size were used because they are potentially mobile due to their stability, small size and negative surface charge. The shapes of elution profiles for colloids and conservative tracers were similar, demonstrating that colloids can migrate over distances of 17 m. The local region of drawdown towards the URL shaft affected colloid migration and, to a lesser extent, conservative tracer migration within the flow field established by the two-well tracer tests. These results indicate that stable colloids, with sizes as small as 20 nm, have different migration properties from dissolved conservative tracers. (author)

Study on liver scintigram using sup(99m)Tc-Sn colloid

International Nuclear Information System (INIS)

Nagase, Katsuya; Maruo, Kuninobu

1975-01-01

First of all, the liver scintigram was taken using 198 Au-colloid in cases of liver diseases, especially cases which seemed to have morphological changes in the liver. Of these cases, in cases which were found to have lesions the liver scintigram was subsequently taken using sup(99m)Tc-Sn colloid. In addition, in order to compare the state of lesions in both liver scintigrams with 198 Au-colloid and sup(99m)Tc-Sn colloid, ultrasonic tomogram was taken at each time. The scintigram using sup(99m)Tc-Sn colloid seemed to more clearly reveal the state of lesions and their sizes in the thin liver regions, especially the right border, the lower border and the left lobe in the liver, compared with 198 Au-colloid scintigram. The lesions in the thick liver tissues, especially the central right lobe, sometimes became unclear using sup(99m)Tc-Sn colloid. Therefore, 198 Au-colloid seemed to be available in these lesions. The scintigram using sup(99m)Tc-Sn colloid was found more useful for the diagnosis of lesions of patients with liver, cirrhosis whom the uptake rate of 198 Au-colloid is poor, compared with 198 Au-colloid scintigram. (Namekawa, K.)

Contamination of pig carcasses with scalding water studied with a radiolabelled colloid

Energy Technology Data Exchange (ETDEWEB)

Jones, E; Nilsson, T; Ekman, L; Oestlund, K [Sveriges Lantbruksuniversitet, Uppsala. Dept. of Clinical Chemistry; Sveriges Lantbruksuniversitet, Uppsala. Abt. fuer Lebensmittelhygiene; Schwedisches Fleischforschungszentrum, Kaevlinge

1979-10-01

Swine carcasses at slaughter are normally scalded after bleeding, i.e. immersed in a hot-water-tank. The present study was made to investigate whether during this treatment scalding water enters the severed vessels via the stick wound and contaminates the carcass. Five experimental pigs were slaughtered and immersed in a scalding vat containing water with a dispersed radiolabelled colloid, sup(99m)Tc-sulphide. After scalding muscles and other tissues from various parts of the body were examined for radioactivity. Scalding water (radioactivity) could be demonstrated in tissues from all investigated parts of the carcass. The highest amounts were found in the lungs and in the large blood vessels. The hygienic significance of the findings is discussed.

Colloidal assemblies modified by ion irradiation

NARCIS (Netherlands)

Snoeks, E.; Blaaderen, A. van; Dillen, T. van; Kats, C.M. van; Velikov, K.P.; Brongersma, M.L.; Polman, A.

2001-01-01

Spherical SiO2 and ZnS colloidal particles show a dramatic anisotropic plastic deformation under 4 MeV Xe ion irradiation, that changes their shape into oblate into oblate ellipsional, with an aspect ratio that can be precisely controlled by the ion fluence. The 290 nm and 1.1 um diameter colloids

The effects of corrosion product colloids on actinide transport

International Nuclear Information System (INIS)

Gardiner, M.P.; Smith, A.J.; Williams, S.J.

1991-11-01

This report assesses the possible effects of colloidal corrosion products on the transport of actinides from the near field of radioactive waste repositories. The desorption of plutonium and americium from colloidal corrosion products of iron and zirconium was studied under conditions simulating a transition from near-field to far-field environmental conditions. Desorption of actinides occurred slowly from the colloids under far-field conditions. Measurements of particle stability showed all the colloids to be unstable in the near field. Stability increased under far-field conditions or as a result of the evolution of the near field. Migration of colloids from the near field is unlikely except in the presence of organic materials. (Author)

Transport and Deposition of Suspended Soil-Colloids in Saturated Sand Columns

DEFF Research Database (Denmark)

Sharma, Anu; Kawamoto, Ken; Møldrup, Per

2011-01-01

Understanding colloid mobilization, transport and deposition in the subsurface is a prerequisite for predicting colloid‐facilitated transport of strongly adsorbing contaminants and further developing remedial activities. This study investigated the transport behavior of soil‐colloids extracted from...... caused tailing of colloid BTCs with higher reversible entrapment and release of colloids than high flow velocity. The finer Toyoura sand retained more colloids than the coarser Narita sand at low pH conditions. The deposition profile and particle size distribution of colloids in the Toyoura sand clearly...

Shape recognition of microbial cells by colloidal cell imprints

NARCIS (Netherlands)

Borovicka, J.; Stoyanov, S.D.; Paunov, V.N.

2013-01-01

We have engineered a class of colloids which can recognize the shape and size of targeted microbial cells and selectively bind to their surfaces. These imprinted colloid particles, which we called "colloid antibodies", were fabricated by partial fragmentation of silica shells obtained by templating

Influence of acidification of circulating water on differential distribution of dispersed phase

Directory of Open Access Journals (Sweden)

Oleksandr B. Gulyaenko

2015-06-01

Full Text Available The paper analyzes the connection between processing technologies of circulating water cooling tower and coagulation-aggregation properties of colloidal particles of the dispersed phase. In circulating water cooling tower when clarifying additional water the reduction of HCO3- and CO32- concentrations happens with corresponding pH increase. Absorption of atmospheric carbon dioxide by cooling tower circulating water offsets this increase. The estimation of the probability of adhesion to the surface of the dispersed phase, distributed in the volume of circulation water, and the heat exchange surface of the condenser for different degrees of evaporation of the coolant is made. The distribution of cooling water micro-disperse particles which are adsorbed on the heat exchange surfaces of the condenser (deposit formation and on the surface of larger particles (particle aggregation reflects the efficiency of applied water treatment technology. It is shown that acidification of additional water facilitates solution of most fine fractions and increases hardness of treated water.

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

Violet-to-Blue Gain and Lasing from Colloidal CdS Nanoplatelets: Low-Threshold Stimulated Emission Despite Low Photoluminescence Quantum Yield

Energy Technology Data Exchange (ETDEWEB)

Diroll, Benjamin T.; Talapin, Dmitri V.; Schaller, Richard D.

2017-02-13

Amplified spontaneous emission (ASE) and lasing from solution-processed materials are demonstrated in the challenging violet-to-blue (430–490 nm) spectral region for colloidal nanoplatelets of CdS and newly synthesized core/shell CdS/ZnS nanoplatelets. Despite modest band-edge photoluminescence quantum yields of 2% or less for single excitons, which we show results from hole trapping, the samples exhibit low ASE thresholds. Furthermore, four-monolayer CdS samples show ASE at shorter wavelengths than any reported film of colloidal quantum-confined material. This work underlines that low quantum yields for single excitons do not necessarily lead to a poor gain medium. The low ASE thresholds originate from negligible dispersion in thickness, large absorption cross sections of 2.8 × 10–14 cm–2, and rather slow (150 to 300 ps) biexciton recombination. We show that under higher-fluence excitation, ASE can kinetically outcompete hole trapping. Using nanoplatelets as the gain medium, lasing is observed in a linear optical cavity. This work confirms the fundamental advantages of colloidal quantum well structures as gain media, even in the absence of high photoluminescence efficiency.

Colloidal superballs

NARCIS (Netherlands)

Rossi, L.

2012-01-01

This thesis is organized in four parts as follows. Part 1 focuses on the synthetic aspects of the colloidal model systems that will be used throughout the work described in this thesis. In Chapter 2 we describe synthetic procedures for the preparation of polycrystalline hematite superballs and

Self-assembled three-dimensional chiral colloidal architecture

Science.gov (United States)

Ben Zion, Matan Yah; He, Xiaojin; Maass, Corinna C.; Sha, Ruojie; Seeman, Nadrian C.; Chaikin, Paul M.

2017-11-01

Although stereochemistry has been a central focus of the molecular sciences since Pasteur, its province has previously been restricted to the nanometric scale. We have programmed the self-assembly of micron-sized colloidal clusters with structural information stemming from a nanometric arrangement. This was done by combining DNA nanotechnology with colloidal science. Using the functional flexibility of DNA origami in conjunction with the structural rigidity of colloidal particles, we demonstrate the parallel self-assembly of three-dimensional microconstructs, evincing highly specific geometry that includes control over position, dihedral angles, and cluster chirality.

Interplay between Colloids and Interfaces : Emulsions, Foams and Microtubes

NARCIS (Netherlands)

de Folter, J.W.J.

2013-01-01

The central theme of this thesis is the interplay between colloids and interfaces. The adsorption of colloids at fluid-fluid interfaces is the main topic and covers Chapters 2-6. Pickering emulsions where colloidal particles act as emulsion stabilizers in the absence of surfactants are studied in a

Colloidal nanocrystals for quality lighting and displays: milestones and recent developments

Directory of Open Access Journals (Sweden)

Erdem Talha

2016-06-01

Full Text Available Recent advances in colloidal synthesis of nanocrystals have enabled high-quality high-efficiency light-emitting diodes, displays with significantly broader color gamut, and optically-pumped lasers spanning the whole visible regime. Here we review these colloidal platforms covering the milestone studies together with recent developments. In the review, we focus on the devices made of colloidal quantum dots (nanocrystals, colloidal quantum rods (nanorods, and colloidal quantum wells (nanoplatelets as well as those of solution processed perovskites and phosphor nanocrystals. The review starts with an introduction to colloidal nanocrystal photonics emphasizing the importance of colloidal materials for light-emitting devices. Subsequently,we continue with the summary of important reports on light-emitting diodes, in which colloids are used as the color converters and then as the emissive layers in electroluminescent devices. Also,we review the developments in color enrichment and electroluminescent displays. Next, we present a summary of important reports on the lasing of colloidal semiconductors. Finally, we summarize and conclude the review presenting a future outlook.

Colloid cysts of the third ventricle

International Nuclear Information System (INIS)

Pina, J.I.; Medrano, J.; Benito, J.L. de; Lasierra, R.; Lopez, S.; Fernandez, J.A.; Villavieja, J.L.

1994-01-01

Colloid cysts (CC) are uncommon cystic endo dermal tumors located in the roof of the third ventricle. The clinical features depend on their capacity for obstructing the foramen of Monro, which results in univentricular or biventricular hydrocephalus. We present three cases of colloid cysts of the third ventricle, diagnosed by CT, reviewing their diagnostic, clinical and pathological features

Colloidal characterization of silicon nitride and silicon carbide

Science.gov (United States)

Feke, Donald L.

1986-01-01

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

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

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

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.

Giant Leaking Colloid Cyst Presenting with Aseptic Meningitis

DEFF Research Database (Denmark)

Bakhtevari, Mehrdad Hosseinzadeh; Sharifi, Guive; Jabbari, Reza

2015-01-01

BACKGROUND: Colloid cysts are benign third ventricle lesions that need to be diagnosed correctly because of their association with sudden death. Chemical or aseptic meningitis is a rare presentation of a colloid cyst. METHODS: We present a case of a 69-year-old man with fever, alteration of mental...... status, and meningismus. Microbiological examination of the cerebrospinal fluid revealed aseptic meningitis. Brain imaging revealed a third ventricular colloid cyst with hydrocephalus. RESULTS: The tumor was resected via endoscopic intervention. There were no persistent operative complications related...... to the endoscopic procedure. CONCLUSIONS: Chemical or aseptic meningitis is an unusual clinical manifestation of a colloid cyst, complicating the differential diagnosis, especially in the elderly....

Colloidal alloys with preassembled clusters and spheres.

Science.gov (United States)

Ducrot, Étienne; He, Mingxin; Yi, Gi-Ra; Pine, David J

2017-06-01

Self-assembly is a powerful approach for constructing colloidal crystals, where spheres, rods or faceted particles can build up a myriad of structures. Nevertheless, many complex or low-coordination architectures, such as diamond, pyrochlore and other sought-after lattices, have eluded self-assembly. Here we introduce a new design principle based on preassembled components of the desired superstructure and programmed nearest-neighbour DNA-mediated interactions, which allows the formation of otherwise unattainable structures. We demonstrate the approach using preassembled colloidal tetrahedra and spheres, obtaining a class of colloidal superstructures, including cubic and tetragonal colloidal crystals, with no known atomic analogues, as well as percolating low-coordination diamond and pyrochlore sublattices never assembled before.

A Study on Liver Scan using 113mIn Colloid

International Nuclear Information System (INIS)

Koh, Chang Soon; Rhee, Chong Hoen; Chang, Kochang; Hong, Chang Gi

1969-01-01

There have been reported numberous cases of liver scanning in use of 198 Au colloid by many investigators, however, one in use of 113m In colloid has not been reported as yet in this country. The dose of 113 mIn for high diagnostic value in examination of each organ was determined and the diagnostic interpretability of liver scanning with the use of 113m In was carefully evaluated in comparison with the results of the liver scanning by the conventionally applied radioisotope. The comparative study of both figures of liver scanning with the use of 113m In colloid and 198 Au colloid delivered following results:1) The liver uptake rate and clearance into peripheral blood were accentuated more in case of 113m In colloid than in case of 198 Au colloid. 2) The interpretability of space occupying lesion in liver scanning with 113m In was also superior to one with 198 Au. 3) The figure of liver scanning with 113m In colloid corresponds not always to the figure with 198 Au. This difference can be explained by difference of phagocytic ability of reticuloendothelial system within liver. 4) In the liver scanning with 113m In colloid, the spleen is also visualized even in normal examine. 5) In the cases of disturbed liver function, uptake is more decreased in use of 113m In colloid than in 198 Au, in the spleen, however, the way is contrary. 6) With use of 113m In colloid, the time required for scanning could be shortened in comparison with 198 Au. 7) The filtration of 113m In colloid for scanning prior to human administration gives an expectation for better scanning figure.

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

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...

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.

Diffusion of organic colloids in compacted bentonite. The influence of ionic strength on molecular size and transport capacity of the colloids

International Nuclear Information System (INIS)

Wold, S.; Eriksen, Trygve E.

2000-09-01

Diffusion of radionuclides in compacted bentonite can be affected by inorganic and organic colloids if the radionuclides form complexes with the colloids. Formation and mobility of the colloid-radionuclide complexes will be governed by the properties of the colloids as well as the competition between complexation and sorption of the radionuclides on bentonite. This report presents the results of experiments with organic colloids humic acid (HA) and lignosulfonate (LS). The aim of the experiments has been to describe the HA and LS properties: size distribution, acidity, sorption on bentonite, diffusivity in compacted bentonite, complexation with strontium, and diffusion of strontium in bentonite in the presence of HA. This study indicates that the diffusion of cationic radionuclides like Sr 2+ is not affected by the presence of HA in high ionic strength solution. In 0.1 M NaClO 4 solution, HA is most probably not available for complexation due to coiling and shielding of the negative sites

Evaluation of colloid transport issues and recommendations for SKI performance assessments

International Nuclear Information System (INIS)

Wickham, S. M.; Bennett, D. G.; Higgo, J. J. W.

2000-08-01

The primary objective of this project was to develop recommendations to SKI for evaluating the potential significance of colloids in performance assessment (PA) studies by: Updating a previous review of the treatment of colloids in PA studies for radioactive waste repositories and to include information on PAs published in the period 1997-1999. We have reviewed sixteen PAs conducted in nine countries and have made the following observations: All PAs include colloid formation and colloid transport in their FEP list. Although some programmes have deferred consideration of colloidal radionuclide transport until further research has been performed, more recent PAs do account for the effects of colloids. PAs of disposal systems in which the waste canister is surrounded by a bentonite buffer do not consider the effect of colloids on the source term. These PAs assume that all colloids are filtered by the bentonite buffer and cannot escape from the near-field. PAs of disposal systems with no bentonite buffer have to account for mobilisation of radionuclides from the waste by colloids. The concentration of colloids that may form in the repository is a key uncertainty. Many PA programmes have modelled colloidal radionuclide transport in the geosphere using one-dimensional transport equations. No PA has included a comprehensive treatment of colloid transport using mechanistic modelling. Some PAs have not undertaken modelling of colloid transport in the geosphere, but have relied instead on arguments that such transport processes will be of low consequence to the performance of the disposal system. Five PAs have shown the effects of colloid transport through the geosphere to be potentially significant. For the disposal of spent nuclear fuel, SKB has developed the KBS-3 concept. For the disposal of long-lived low-level and intermediate-level radioactive waste, SKB has developed the SFL 3-5 concept. In the SFL 3-5 concept, waste is placed in underground disposal caverns and

Reversibility of sorption of plutonium-239 onto hematite and goethite colloids

International Nuclear Information System (INIS)

Lu, N.; Cotter, C.R.; Kitten, H.D.; Bentley, J.; Triay, I.R.

1998-01-01

Laboratory batch sorption experiments were conducted to evaluate: (1) sorption of plutonium-239 ( 239 Pu) on different iron oxide colloids (hematite and geothite), (2) sorption kinetics of colloidal Pu(IV) and soluble Pu(V) onto these two colloids, and (3) desorption of colloidal Pu(IV) and soluble Pu(V) from 239 Pu-loaded colloids as a function of time. Natural groundwater and carbonate-rich synthetic groundwater were used in this study. To examine the possible influence of bicarbonate on 239 Pu sorption, an additional set of experiments was conducted in sodium nitrate (NaNO 3 ) solutions under carbon dioxide free environments. Our results show that colloidal Pu(IV) as well as soluble Pu(V) was rapidly adsorbed by hematite and goethite colloids in both natural and synthetic groundwater. The amount of 239 Pu adsorbed by both iron oxide colloids in synthetic groundwater was higher than in natural groundwater. The presence of carbonate did not influence the sorption of 239 Pu. While sorption of soluble Pu(V) is a slow process, sorption of colloidal Pu(IV) occurs rapidly. Desorption of Pu from iron oxide colloids is much slower than the sorption processes. Our findings suggest that different sorption and desorption behaviors of 239 Pu by iron oxide colloids in groundwater may facilitate the transport of 239 Pu along potential flowpaths from the areas contaminated by radionuclide and release to the accessible environment. (orig.)

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.

A differential dielectric spectroscopy setup to measure the electric dipole moment and net charge of colloidal quantum dots

Energy Technology Data Exchange (ETDEWEB)

Kortschot, R. J.; Bakelaar, I. A.; Erné, B. H.; Kuipers, B. W. M., E-mail: B.W.M.Kuipers@uu.nl [Van ' t Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Padualaan 8, 3584 CH Utrecht (Netherlands)

2014-03-15

A sensitive dielectric spectroscopy setup is built to measure the response of nanoparticles dispersed in a liquid to an alternating electric field over a frequency range from 10{sup −2} to 10{sup 7} Hz. The measured complex permittivity spectrum records both the rotational dynamics due to a permanent electric dipole moment and the translational dynamics due to net charges. The setup consists of a half-transparent capacitor connected in a bridge circuit, which is balanced on pure solvent only, using a software-controlled compensating voltage. In this way, the measured signal is dominated by the contributions of the nanoparticles rather than by the solvent. We demonstrate the performance of the setup with measurements on a dispersion of colloidal CdSe quantum dots in the apolar liquid decalin.

Colloid-templated multisectional porous polymeric fibers.

Science.gov (United States)