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Surface Charge Density (surface + charge_density)
Selected AbstractsMicrostructure of microemulsion in MEEKCELECTROPHORESIS, Issue 4 2010Yuhua Cao Abstract The influences of the composition of microemulsion on the microstructure including dimensions and , potentials of microdroplets were measured in details. The average dynamic dimension of microdroplets was measured by dynamic laser light scattering, and , potential was determined to characterize average surface charge density of microdroplets. The experiment results showed that increase of the amount of surfactant resulted in decrease of microdroplet size but almost invariant , potential, which would enlarge migration time of the microdroplet in MEEKC. With increment of cosurfactant concentration, the microdroplet size had an increasing trend, whereas the , potential decreased. Thus, observed migration velocity of microdroplets increased, which made the separation window in MEEKC shortened. Neither dimension nor , potential of microdroplets changed by varying both the type and the amount of the oil phase. Adding organic solvent as modifier to microemulsion did not change the microdroplet size, but lowered , potential. The migration time of microdroplet still became larger, since EOF slowed down owing to organic solvent in capillary. So, besides increment of surfactant concentration, organic additive could also enlarge the separation window. Increase of cosurfactant concentration was beneficial for separation efficiency thanks to the looser structure of swollen microdroplet, and the peak sharpening might compensate for the resolution and peak capacity owing to a narrow separation window. Except the oil phase, tuning the composition of microemulsion would change the microstructure, eventually could be exploited to optimize the resolution and save analysis time in MEEKC. [source] Analysis of effect of electrolyte types on electrokinetic energy conversion in nanoscale capillariesELECTROPHORESIS, Issue 3 2010Reiyu Chein Abstract An analytical study on the effect of electrolyte types on the electrokinetic energy conversion is presented using nanoscale cylindrical capillary, which is either positively or negatively charged. The sign of surface charge determines the role and concentration magnitude of ions in the capillary and the energy conversion performance. Our study shows that the electrokinetic energy conversion performance (maximum efficiency, pressure rise and streaming potential) are approximately identical for 1:1 (KCl), 2:1 (CaCl2) and 3:1 (LaCl3) electrolytes when capillary is positively charged. For negatively charged capillary, energy conversion performance degrades significantly with the increase of counter-ion valence. For both positively and negatively charged capillaries, higher maximum efficiency can be resulted in low bulk concentration and surface charge density regimes. However, high maximum pressure rise generation for the pumping is found in the low bulk concentration and high surface charge density regimes. For the electric power generation, higher maximum streaming potential is found when both bulk concentration and surface charge density are low. [source] A model incorporating the diffuse double layer to predict the electrical conductivity of bulk soilEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2007M. A. Mojid Summary A model has been developed to predict the electrical conductivity of bulk soil. The total soil-water content is divided into free water and water in the diffuse double layer (DDL) around clay particles. These two fractions of soil water conduct electrical current through the soil and are assumed to act in parallel with the soil solid. The volume of water in the DDL is evaluated from the surface area of the clay and the thickness of the DDL. The surface area of the clay is estimated from its cation exchange capacity (CEC) and surface charge density. A transmission coefficient correcting for the effect of the tortuous flow path of current through the soil, and a proportionality constant relating the electrical conductivity of water in the DDL to that of free water, are included in the model. The transmission coefficient is a function of the contents of water and clay and has been modelled in terms of these factors. The values of the proportionality constant and those relating to the transmission coefficient were optimized for five different soils. The electrical conductivities of the five soils estimated by the model compare well with the measured values, which, however, deviate systematically from predictions by the three-component model of Rhoades et al. [source] Physico-chemical requirements for cellular uptake of pAntp peptideFEBS JOURNAL, Issue 5 2001Role of lipid-binding affinity The pAntp peptide, corresponding to the third helix of the Antennapedia homeodomain, is internalized by a receptor-independent process into eucaryotic cells. The precise mechanism of entry remains unclear but the interaction between the phospholipids of plasma membrane and pAntp is probably involved in the translocation process. In order to define the role of peptide,lipid interaction in this mechanism and the physico-chemical properties that are necessary for an efficient cellular uptake, we have carried out an Ala-Scan mapping. The peptides were labeled with a fluorescent group (7-nitrobenz-2-oxo-1,3-diazol-4-yl-; NBD) and their cell association was measured by flow cytometry. Furthermore, we determined the fraction of internalized peptide by using a dithionite treatment. Comparison between cell association and cell uptake suggests that the affinity of pAntp for the plasma membrane is required for the import process. To further investigate which are the physico-chemical requirements for phospholipid-binding of pAntp, we have determined the surface partition coefficient of peptides by titrating them with phospholipid vesicles having different compositions. In addition, we estimated by circular dichroism the conformation adopted by these peptides in a membrane-mimetic environment. We show that the phospholipid binding of pAntp depends on its helical amphipathicity, especially when the negative surface charge density of phospholipid vesicles is low. The cell uptake of pAntp, related to lipid-binding affinity, requires a minimal hydrophobicity and net charge. As pAntp does not seem to translocate through an artificial phospholipid bilayer, this might indicate that it could interact with other cell surface components or enters into cells by a nonelucidated biological mechanism. [source] Binding of rat brain hexokinase to recombinant yeast mitochondriaFEBS JOURNAL, Issue 10 2000Identification of necessary physico-chemical determinants The association of rat brain hexokinase with heterologous recombinant yeast mitochondria harboring human porin (Yh) is comparable to that with rat liver mitochondria in terms of cation requirements, cooperativity in binding, and the effect of amphipathic compounds. Mg2+, which is required for hexokinase binding to all mitochondria, can be replaced by other cations. The efficiency of hexokinases, however, depends on the valence of hydrophilic cations, or the partition of hydrophobic cations in the membrane, implying that these act by reducing a prohibitive negative surface charge density on the outer membrane rather than fulfilling a specific structural requirement. Macromolecular crowding (using dextran) has dual effects. Dextran added in excess increases hexokinase binding to yeast mitochondria, according to the porin molecule they harbor. This effect, significant with wild-type yeast mitochondria, is only marginal with Yh as well as rat mitochondria. On the other hand, an increase in the number of hexokinase binding sites on mitochondria is also observed. This increase, moderate in wild-type organelles, is more pronounced with Yh. Finally, dextran, which has no effect on the modulation of hexokinase binding by cations, abolishes the inhibitory effect of amphipathic compounds. Thus, while hexokinase binding to mitochondria is predetermined by the porin molecule, the organization of the latter in the membrane plays a critical role as well, indicative that porin must associate with other mitochondrial components to form competent binding sites on the outer membrane. [source] Water-elutability of nucleic acids from metal-chelate affinity adsorbents: enhancement by control of surface charge density,JOURNAL OF MOLECULAR RECOGNITION, Issue 4 2006Joseph Y. Fu Abstract Immobilized metal affinity chromatography (IMAC) is widely used for purification of proteins, especially "hexahistidine-tagged" recombinant proteins. We previously demonstrated the application of IMAC to selective capture of nucleic acids, including RNA, selectively-denatured genomic DNA, and PCR primers through interactions with purine bases exposed in single-stranded regions. We also found that the binding affinity of nucleic acids for IMAC adsorbents can be increased several-fold by addition of 20 volume% of neutral additives such as ethanol or DMSO. In the present work, it is demonstrated that bound nucleic acids can be effectively eluted with water instead of the usual imidazole-containing competitive eluants, when the surface density of negative charges is enhanced by operation at alkaline pH, or by deliberate metal-underloading of the anionic chelating ligands. With enhanced negative surface charge density, nucleic acid adsorption can be made strongly dependent on the presence of adsorption-promoting additives and/or repulsion-shielding salts, and removal of these induces elution. Complete water-elutability is demonstrated for baker's yeast RNA bound to 10% Cu(II)- underloaded IDA Chelating Sepharose in a binding buffer of 20,mM HEPES, 240,mM NaCl, pH,7. Water elutability will significantly enhance the utility of IMAC in nucleic acid separations. Copyright © 2006 John Wiley & Sons, Ltd. [source] Composition-Size Effects in Nickel,Zinc Ferrite Nanoparticles Prepared by Aqueous CoprecipitationJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2008Brian T. Naughton Nickel,zinc ferrite nanoparticles across the solid solution range, Ni1,xZnxFe2O4, from nickel ferrite to zinc ferrite were prepared by aqueous precipitation of mixed nitrate solutions at the same pH of 12.3. There is a linear relationship between the nanoparticle diameter and composition, decreasing with increasing zinc concentration across the solid solution. The nanoparticles are highly resistant to coarsening and some of them are faceted, suggesting that they are close to thermodynamic equilibrium. Measurements of the surface charge density of the nanoparticles, based on simultaneous conductimetric and potentiometeric titration, are presented as a function of composition for the zinc-rich compositions. A trend exists between the surface charge density and the zinc concentration, suggesting that they may be stabilized by charge. [source] Biological and Optical Properties of Fluorescent Nanoparticles Developed for Intravascular ImagingMICROSCOPY RESEARCH AND TECHNIQUE, Issue 9 2007Dino J. Ravnic Abstract Intravascular tracers in the blood circulation can provide a description of the flow field over time and space. To address the limitations of existing intravascular tracers, we have developed fluorescent nanoparticles capable of providing detailed information regarding the intravascular flow field. The nanoparticles were designed to maximize plasma half-life as well as minimize interactions with other blood components. The bioavailability of the particles in the blood circulation required nanoscale size and low surface charge density. Intravital imaging of nanoparticles in the microcirculation demonstrated that the fluorescence intensity of the nanoparticles was a major determinant of both temporal and spatial resolution of the flow field. We conclude that nanoparticles prepared with these physical and optical properties can provide an accurate description of the localized intravascular flow field. Microsc. Res. Tech., 2007. © 2007 Wiley-Liss, Inc. [source] Size and Structure Characterization of Dye Flocs during Coagulation of Reactive Black 5 DyePARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 2 2006Marta Janeczko Abstract This paper deals with results from laboratory scale experiments with model dye effluents comprising of the commercially used textile diazo dye, CI "Reactive Black 5", coagulated with ZETAG type primary coagulants. Size and structure analysis of flocs in coagulated dye sludge was undertaken in order to evaluate their separation abilities. The particle size distribution was estimated by use of a Galai CIS-100 particle counting system working on a time-of-transition principle, while their fractal dimension was obtained from laser scattering instrument in LALS mode. An image analysis of the flocculated dye-sludge has also been carried out. In parallel to the flocs characterization, the measurement of surface charge density of coagulated dye sludge was performed with the aim of linking surface charge data with the floc characteristics, and on this basis, to outline the predominant mechanism of color removal. It was found that flocs produced at optimal dosage are characterized by large sizes and a high value of fractal dimension, which is manifested in a very good level of color removal by sedimentation. The evident correlation between the surface charge density progression of coagulated dye flocs and color removal, suggests adsorption and charge neutralization as the predominant mechanism of dye destabilization. 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