


Vol 79, No 4 (2017)
- Year: 2017
- Articles: 15
- URL: https://journal-vniispk.ru/1061-933X/issue/view/12575
Review
Mineral liquid crystals
Abstract
The contemporary state of studying mineral liquid crystals has been analyzed. Such crystals are lyotropic aqueous or water–organic colloidal solutions, the dispersed phases of which are represented by nano- and microsized crystalline particles. The methods of production, structure, and physicochemical properties of these systems, as well as the influence of electric and magnetic fields on them, have been discussed in detail.



Article



Colloid chemical characteristics of nanoporous glasses with different compositions in solutions of simple and organic electrolytes. 3. Calculation of electrochemical characteristics of membranes in terms of a homogeneous model
Abstract
The electrosurface characteristics of nanoporous glass membranes–ion concentrations in pores with taking into account the specificity of counterions, electrokinetically mobile charge, the convective component of pore solution electrical conductivity, electroosmotic mobility of a liquid in the field of streaming potential and ion mobilities in pore space–were calculated within the homogeneous model. The effects of the type of counterion (sodium, potassium, ammonium, tetramethylammonium, and tetraethylammonium ions), solution concentration, glass composition, and pore size on the equilibrium and transport characteristics of membrane systems have been analyzed. A method for the determining of electrolyte activity coefficients in the membranes has been proposed.



Filtration of nanoaerosols through a granular layer
Abstract
Diffusion deposition of nanoparticles in model granular filters with different structures has been considered at low Reynolds numbers. On the basis of a three-dimensional flow field calculated for layers of granules, nanoparticle-collection efficiences have been determined for the granules in a wide range of the Peclet diffusion numbers. The interference of the layers has been studied, and approximation equations have been derived for calculating the pressure drop and the nanoparticle-collection efficiency.



Nanoparticle deposition in granular filters at Reynolds numbers higher than unity
Abstract
The influence of the inertia of a viscous incompressible liquid flow on the viscous drag and diffusion deposition of particles in model granular filters at Reynolds numbers higher than unity, Re > 1, has been considered. The granule drag forces and particle-collection efficiencies in isolated layers with square and hexagonal packings of granules have been calculated. The influence on each other of approaching monolayers of granules on pressure drop and nanoparticle deposition has been studied. It has been shown that, at Re > 1, the collection efficiency dramatically increases due to the effect of interception.



Dynamics simulation of disperse systems in the presence of a structure-related mechanical barrier resulting from surfactant adsorption
Abstract
A computer model has been developed to refine the notions of the kinetics of structural transformations in surfactant-modified disperse systems, the mechanism of the influence of adsorption layers on viscosity, conditions of aggregation, and evolution of nonuniformities in microstructures. Classical concepts of the structure-related mechanical barrier providing disperse systems with stability to aggregation, as well as the criterion of adsorption-layer breakdown upon interparticle collisions under dynamic conditions, have been used. It has been shown that adsorption-layer breakdown under dynamic conditions may lead to the appearance of an extreme in the viscosity curve of a disperse system. The combined effect of additives of surfactants with different molecular masses successively added to the systems has been studied via taking into account the influence of surfactant adsorption layers on the dynamics of contact interactions. The simulation results make it possible to optimize the regulation of structure-related rheological properties of dispersions so as to decrease their apparent viscosity with a simultaneous increase in the uniformity of the structure.



A study of cryostructuring of polymer systems. 45. Effect of porosity of dispersed filler on physicochemical characteristics of composite poly(vinyl alcohol) cryogels
Abstract
Composite cryogels simulating the properties of waterproof screens of hydraulic structures, such as protruding dykes and dams, have been obtained by a cryogenic treatment (freezing at –10…–30°C followed by incubation in the frozen state for 12 h and defrosting at a rate of 0.03°C/min) of suspensions of calcium-carbonate-containing (marble or coquina) or cellulose-containing (microcrystalline cellulose or sawdust) particles in aqueous poly(vinyl alcohol) solutions. Viscometric examinations of initial suspensions have shown that adhesion contacts arise between filler particles, as well as discrete and continuous phases, already at the stage of suspension preparation, thereby affecting the properties of resulting cryogels. This is most pronounced when high-porosity sawdust is used as a filler. It has been shown that all the dispersed materials used in the work are “active” fillers for poly(vinyl alcohol) cryogels, these fillers increasing the rigidity of the formed composites. Therewith, porous particles, into which the polymer solution can penetrate, are more efficient. The dependence of the composite rigidity on the temperature of the cryogenic treatment has, as a rule, a bell-shaped pattern with a maximum in the region of –20°C. Being tested for water permeability, the obtained model composite cryogels have exhibited pronounced antifiltration properties (the filtration coefficient is ≤(1–2) × 10–9 cm/s), thus indicating that such materials are promising for solving problems relevant to the protection of fascine hydraulic structures from erosion with snow water.



Interaction between polymer capsules with hydrophobic cores and a model cellular membrane at an air–water interface
Abstract
Submicrocapsules have been prepared from diethylaminoethyl dextran and xanthan gum on oil cores by ultrasonic treatment. These capsules have been modified with poly-L-lysine via electrostatic adsorption. The behavior of the capsules has been investigated at an air–water interface after their introduction into the aqueous subphase. The interaction of the capsules with a 1,2-dimyristoyl-sn-glycero-3-phosphocholine monolayer formed on the water surface (model cellular membrane) has been studied both upon their introduction under the condensed monolayer and with the use of a dilute colloidal solution of the capsules as a subphase.



Mechanisms of depinning accompanying evaporation of colloidal dispersion droplets
Abstract
Experiments have been performed to clarify the mechanism of depinning, i.e., the onset of the movement of the menisci of evaporating dispersion droplets under the conditions of the formation of ringshaped deposits (the coffee-ring effect). The influence of the nature and concentration of dispersed particles on depinning has been studied. It has been shown that there are three main effects responsible for depinning. The first effect is due to the hysteresis of droplet contact angle, the second one results from the influence of the particles on the surface tension of a dispersion, and the third effect is caused by the formation of a dense gel in the meniscus region. A relation has been revealed between the mechanisms being realized and scenarios of droplet evaporation.



Methodological features of mass-spectrometric studies of oxidized metal surfaces
Abstract
Clustering of silver halides under the conditions of photoionization has previously been studied by laser desorption/ionization mass spectrometry. Some features of desorption/ionization of silver halides from different metal surfaces (stainless steel and different partially oxidized aluminum alloys) are discussed in this study. The data on the m/z values determination accuracy, resolving power, ionization efficiency, and distortion of isotope distribution in the studies of oxidized surfaces are statistically generalized. It is shown that the results can be used to gain insight into the chemical nature and morphology of examined surfaces and, in particular, to plot diagrams for distribution of analyzed compounds over the surfaces.



On the Schroeder paradox for nonionogenic polymers
Abstract
The well-known Schroeder paradox, i.e., the difference in the degrees of swelling of nonionogenic polymers occurring at equilibrium with liquid and vapor phases, has been discussed. A simple example has been presented, which illustrates the unavoidability of different degrees of swelling for a polymer brought into contact with vapor and liquid phases. A simple mechanism has been proposed for the excess swelling of a nonionogenic polymer immersed in a liquid phase, this mechanism being associated with the action of van der Waals and solvation forces at a polymer/solvent interface. The estimation of the contribution from the van der Waals interaction to the “excess” swelling has shown that the predicted values of the “excess” swelling agree with the data of real experiments.



The mechanism of action and place of application of capillary forces
Abstract
The question of the mechanism of action and the place of application of capillary forces has been discussed. It has been shown that the conventional notions of the character of capillary forces are often contradictory. A molecular-kinetic approach has been employed to determine the places of application of capillary forces and the mechanism of their action.



Hydrogen diffusion transfer through an asymmetric three-layer vanadium membrane
Abstract
Hydrogen diffusion transfer through a three-layer membrane has been studied within the framework of the lattice model under the Bragg‒Williams approximation. A set of equations describing hydrogen transfer through a vanadium membrane coated with thin palladium layers has been derived taking into account the interactions of hydrogen atoms in the membrane layers. The obtained equations have been solved using the Mathcad-14 software package. It has been shown that the interaction between hydrogen atoms has a significant influence on hydrogen permeability at near-atmospheric pressures. It has been found that the permeability of the vanadium membrane is markedly higher than that of a palladium one at the same thickness. The effect of asymmetric vanadium membrane embrittlement has been shown to depend on the location of palladium layers with different thicknesses. The embrittlement of the vanadium membrane begins at higher pressures, when a thicker palladium layer is located at the inlet. It has been revealed that, for asymmetric membranes, the value of the diffusion flux of hydrogen atoms may depend on the transfer direction. At the same membrane thickness, the permeability of the asymmetric membrane is actually equal to that of a symmetrical membrane, provided that a thicker palladium layer is located at the inlet. At the opposite orientation, of the permeability of the asymmetric membrane is lower than that of the symmetric one.



Diffusion of electrolytes of different natures through the cation-exchange membrane
Abstract
Diffusion of different electrolytes through a negatively charged (cation-exchange) membrane into distilled water has been studied. It has been established theoretically (with no regard to the presence of diffusion layers) that the integral diffusion permeability coefficient of an electrolyte depends on the diffusion coefficients and the ratio between the charge numbers of a cation–anion pair, the ratio between the density of charges fixed in the membrane and electrolyte concentration, and the averaged coefficient of equilibrium distribution of cation−anion ion pairs in the membrane matrix. It has been found that, when co-ions have a higher mobility, the dependence of diffusion permeability on electrolyte concentration passes through a maximum. Derived equations have been compared with experimental dependences of the diffusion permeability of an MC-40 membrane with respect to different solutions of inorganic 1: 1 and 2: 1 electrolytes. The developed method has been shown to be applicable for describing diffusion of any electrolytes (including asymmetric ones) through arbitrary uniformly charged membranes.



Short Communications
Counterion condensation in hydrosols of single-crystalline detonation nanodiamond particles obtained by air annealing of their agglomerates
Abstract
The pattern of previously recorded dependences of the specific surface charge and electrophoretic mobility of monodisperse detonation nanodiamond particles on pH of aqueous KCl solutions suggests that counterions are condensed on the particle surface. Counterion condensation is considered in terms of the Levin model, and the experimental ratios between the densities of the electrokinetic and surface charges of dispersed particles, as well as the fractions of condensed counterions, are calculated as depending on pH and KCl concentration in nanodiamond hydrosols. The obtained dependences lead to the conclusion that counterion condensation on the surface of detonation nanodiamond particles does indeed take place.


