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Colloidal Material (colloidal + material)
Selected AbstractsConcentration dependency of biota-sediment accumulation factors for chlorinated dibenzo- p -dioxins and dibenzofurans in dungeness crab (Cancer magister) at marine pulp mill sites in British Columbia, CanadaENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2000Walter J. Cretney Abstract Biota-sediment accumulation factors (BSAFs) for some chlorinated dibenzo- p -dioxin and dibenzofuran congeners (PCDD/Fs) in Dungeness crab (Cancer magister) hepatopancreas and associated sediments are concentration independent as required by equilibrium partition models. In particular 2, 3, 7, 8-tetrachlorodibenzo- p -dioxin (2, 3, 7, 8-TCDD), 2, 3, 7, 8-tetrachlorodibenzofuran, the 2, 3, 7, 8-substituted pentachlorodibenzofurans, and the non-2, 3, 7, 8-hexachlorodibenzofurans (HxCDFs) seem to fall into this group. The BSAFs for other isomers exhibit significant, nonlinear variations with sediment or crab PCDD/F concentrations. For some of these other isomers (e.g., the non-2, 3, 7, 8 TCDDs and possibility the 2, 3, 7, 8-substituted HxCDFs), association of a variable fraction of the total present with soot carbon may provide a satisfactory explanation for the concentration behavior. For the HxCDDs we propose that the nonlinear concentration behavior may arise from the thermodynamic properties of fluids confined in hydrophobic voids within particulate and colloidal material produced by the pulp mills. The nonlinear relationship between BSAFs and PCDD/F concentrations greatly complicates prediction of the potential for dioxin and furan bioaccumulation in crabs and the formulation of sediment quality criteria. We provide a nonlinear equation relating toxic equivalency and sediment concentrations. [source] Enhanced Optical Properties and Opaline Self-Assembly of PPV Encapsulated in Mesoporous Silica SpheresADVANCED FUNCTIONAL MATERIALS, Issue 23 2009Timothy L. Kelly Abstract A new poly(p -phenylenevinylene) (PPV) composite material has been developed by the incorporation of insoluble PPV polymer chains in the pores of monodisperse mesoporous silica spheres through an ion-exchange and in situ polymerization method. The polymer distribution within the resultant colloidal particles is characterized by electron microscopy, energy dispersive X-ray microanalysis, powder X-ray diffraction, and nitrogen adsorption. It was found that the polymer was selectively incorporated into the mesopores of the silica host and was well distributed throughout the body of the particles. This confinement of the polymer influences the optical properties of the composite; these were examined by UV,vis and fluorescence spectroscopy and time-correlated single-photon counting. The results show a material that exhibits an extremely high fluorescence quantum yield (approaching 85%), and an improved resistance to oxidative photobleaching compared to PPV. These enhanced optical properties are further complemented by the overall processability of the colloidal material. In marked contrast to the insolubility of PPV, the material can be processed as a stable colloidal dispersion, and the individual composite spheres can be self-assembled into opaline films using the vertical deposition method. The bandgap of the opal can be engineered to overlap with the emission band of the polymer, which has significant ramifications for lasing. [source] Ultra scale-down prediction using microwell technology of the industrial scale clarification characteristics by centrifugation of mammalian cell brothsBIOTECHNOLOGY & BIOENGINEERING, Issue 2 2009A.S. Tait Abstract This article describes how a combination of an ultra scale-down (USD) shear device feeding a microwell centrifugation plate may be used to provide a prediction of how mammalian cell broth will clarify at scale. In particular a method is described that is inherently adaptable to a robotic platform and may be used to predict how the flow rate and capacity (equivalent settling area) of a centrifuge and the choice of feed zone configuration may affect the solids carry over in the supernatant. This is an important consideration as the extent of solids carry over will determine the required size and lifetime of a subsequent filtration stage or the passage of fine particulates and colloidal material affecting the performance and lifetime of chromatography stages. The extent of solids removal observed in individual wells of a microwell plate during centrifugation is shown to correlate with the vertical and horizontal location of the well on the plate. Geometric adjustments to the evaluation of the equivalent settling area of individual wells (,M) results in an improved prediction of solids removal as a function of centrifuge capacity. The USD centrifuge settling characteristics need to be as for a range of equivalent flow rates as may be experienced at an industrial scale for a machine of different shear characteristics in the entry feed zone. This was shown to be achievable with two microwell-plate based measurements and the use of varying fill volumes in the microwells to allow the rapid study of a fivefold range of equivalent flow rates (i.e., at full scale for a particular industrial centrifuge) and the effect of a range of feed configurations. The microwell based USD method was used to examine the recovery of CHO-S cells, prepared in a 5,L reactor, at different points of growth and for different levels of exposure to shear post reactor. The combination of particle size distribution measurements of the cells before and after shear and the effect of shear on the solids remaining after centrifugation rate provide insight into the state of the cells throughout the fermentation and the ease with which they and accumulated debris may be removed by continuous centrifugation. Hence bioprocess data are more readily available to help better integrate cell culture and cell removal stages and resolve key bioprocess design issues such as choice of time of harvesting and the impact on product yield and contaminant carry over. Operation at microwell scale allows data acquisition and bioprocess understanding over a wide range of operating conditions that might not normally be achieved during bioprocess development. Biotechnol. Bioeng. 2009; 104: 321,331 © 2009 Wiley Periodicals, Inc. [source] The two-Yukawa model and its applications: the cases of charged proteins and copolymer micellar solutionsJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2007Sow-Hsin Chen Charged and uncharged colloidal systems are known from experiment to display an extremely rich phase behavior, which is ultimately determined by the effective pair potential between particles in solution. As a confirmation, the recent striking observation of an equilibrium cluster phase in charged globular protein solutions [Stradner, Sedgwick, Cardinaux, Poon, Egelhaaf & Schurtenberger (2004). Nature, 432, 492,495] has been interpreted as the effect of competing short-range attractive and long-range repulsive interactions. The `two-Yukawa (2Y) fluid' model assumes an interparticle potential consisting of a hard core plus an attractive and a repulsive Yukawa tail. We show that this rather simple model can indeed explain satisfactorily the structural properties of diverse colloidal materials, measured in small-angle neutron scattering (SANS) experiments, including the cases of equilibrium cluster formation and soft-core repulsion. We apply this model to the analysis of SANS data from horse-heart cytochrome c protein solutions (whose effective potential can be modeled as a hard-sphere part plus a short-range attraction and a weaker screened electrostatic repulsion) and micellar solutions of a triblock copolymer (whose effective potential can be modeled as a hard-sphere part plus a repulsive shoulder and a short-range attraction). The accuracy of the 2Y model predictions is successfully tested against Monte Carlo simulations in both cases. [source] Probing interactions by means of pulsed field gradient nuclear magnetic resonance spectroscopy,MAGNETIC RESONANCE IN CHEMISTRY, Issue S1 2008Sara Cozzolino Abstract Molecular self-diffusion coefficients (D) of species in solution are related to size and shape and can be used for studying association phenomena. Pulsed field gradient nuclear magnetic resonance (PFG-NMR) spectroscopy has been revealed to be a powerful analytical tool for D measurement in different research fields. The present work briefly illustrates the use of PFG-NMR for assessing the existence of interactions in very different chemical systems: organic and organometallic compounds, colloidal materials and biological aggregates. The application of PFG-NMR is remarkable for understanding the role of anions in homogenous transition metal catalysis and for assessing the aggregation behaviour of biopolymers in material science. Copyright © 2008 John Wiley & Sons, Ltd. [source] | |||||||||||||