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BV Zhmud

Publications and source records attributed to BV Zhmud.

6 recordsLinked to original sources

Micellar Interactions in Nonionic/Ionic Mixed Surfactant Systems.

To study the influence of the chemical nature of headgroups and the type of counterion on the process of micellization in mixed surfactant systems, the cmc's of several binary mixtures of surfactants with the same length of hydrocarbon tail but with different headgroups have been determined as a function of the monomer composition using surface tension measurements. Based on these results, the interaction parameter between the surfactant species in mixed micelles has been determined using the pseudophase separation model. Experiments were carried out with (a) the nonionic/anionic C(12)E(6)/SDS ((hexa(ethyleneglycol) mono-n-dodecyl ether)/(sodium dodecyl sulfate)), (b) amphoteric/anionic DDAO/SDS ((dodecyldimethylamine oxide)/(sodium dodecyl sulfate)), and (c) amphoteric/nonionic C(12)E(6)/DDAO mixed surfactant systems. In the case of the mixed surfactant systems containing DDAO, experiments were carried out at pH 2 and pH 8 where the surfactant was in the cationic and nonionic form, respectively. It was shown that the mixtures of the nonionic surfactants with different kinds of headgroups exhibit almost ideal behavior, whereas for the nonionic/ionic surfactant mixtures, significant deviations from ideal behavior (attractive interactions) have been found, suggesting binding between the head groups. Molecular orbital calculations confirmed the existence of the strong specific interaction between (1) SDS and nonionic and cationic forms of DDAO and between (2) C(12)E(6) and the cationic form of DDAO. In the case for the C(12)E(6)/SDS system, an alternative mechanism for the stabilization of mixed micelles was suggested, which involved the lowering in the free energy of the hydration layer. Copyright 2000 Academic Press.

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Dynamics of Capillary Rise.

An overview and detailed analysis of the classical theory of capillarity is presented. A number of known equations of capillary rise dynamics are shown to be different limiting cases of one rather general equation. Some internal inconsistencies of the classical equations are pointed out. The role of nonlinear dissipation and flow pattern effects in the front zone of the liquid column and near the capillary entrance is discussed. Numerical simulations and experimental data demonstrating some characteristic types of dynamic behavior predicted by the theory are reported. Special attention is paid to the capillary rise of surfactant solutions. As applied to this special case, the existing theory is substantially elaborated by setting up a closed system of equations describing the surfactant transport and relaxation processes in the adsorption layer. A simplified relation for the capillary rise dynamics in the case of strong depletion of the interfacial region is obtained, which is in qualitative agreement with the experimental behavior. Copyright 2000 Academic Press.

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Dissolution Kinetics of Silicon Nitride in Aqueous Suspension.

A general system of equations describing the dissolution of polydisperse solids having a porous particulate structure is set up and applied to study the hydrolysis and subsequent dissolution of silicon nitride powder in aqueous suspensions. The latter process has been found to follow a simple kinetic equation, c(t) = c(s)[1 - exp(-kt)], with the dissolution rate constant k = 2.3 x 10(-6) s(-1) (or 2.5 x 10(-11) mol m(-2) s(-1)) and the saturation concentration c(s) = 3.2 mmol dm(-3) at room temperature and pH 9. The role of diffusion is unimportant, so the concentration of soluble species in pore water changes almost simultaneously with their concentration in the surrounding solution. Copyright 1999 Academic Press.

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Evaluation of Surface Ionization Parameters from AFM Data.

A new application of atomic force microscopy (AFM) for evaluation of surface ionization parameters on the basis of a charge-regulation model is demonstrated. Interactions between symmetrical silicon nitride and silica surfaces have been measured in aqueous electrolytic solutions at different pHs and separations from a few Debye lengths down to zero. The obtained experimental data are reported and interpreted on a quantitative level in the framework of Derjaguin's approximation; the computational procedure used for this purpose is outlined. Surface charge density, surface potential, and species concentrations are calculated as functions of pH and separation, unveiling the limits of applicability of classical constant-charge and constant-potential approximations. The integrity of the results on the charge properties of interacting surfaces is discussed in reference to electrokinetic and titration data, potential problems caused by the existence of non-DLVO forces and surface irregularities being highlighted. Copyright 1998 Academic Press.

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Probing the Sol-Gel Conversion in the Tetraethoxysilane/Alcohol/Water System with the Aid of Diffusion-Controlled Fluorescence Quenching

The sol-gel conversion in the tetraethoxysilane/alcohol/water system can be probed by means of the diffusion-controlled fluorescence quenching of Py* by Cu2+ ions. In the course of tetraethoxysilane hydrolysis, the viscosity of the system increases, thereby causing the quenching rate to decrease and the mean lifetime of the excited state to elongate dramatically as the system approaches the gel-point. Incorporating the equation proposed by Vogelsberger et al. (1992) for the time-dependence of the viscosity of gelating systems into the Smoluchowsky kinetic equation, an equation has been proposed to describe the observed time-dependence of the Py* lifetime. Copyright 1997 Academic Press. Copyright 1997Academic Press

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Electrical Double Layer and Charge Regulation for a Homotattic Surface

The spatial distribution of the electrostatic potential near a charge-regulated homotattic surface containing zones with altering ionization ability is studied in the framework of the Debye approximation. In contrast to the constant-charge case traditionally discussed in the literature, charge regulation causes inhomogeneity of the surface charge distribution within each zone at the surface. Possible methods of solution of the charge regulation problem are outlined, and the results of a model calculation are reported.

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