


Vol 87, No 1 (2025)
Articles
Effect of conditions for obtaining detonation nanodiamond on surface composition and stability of its aqueous sols
Abstract
In present work, the effect of additional treatment of detonation nanodiamond (DND) powder of basic purification on the surface composition of DND particles, their electrokinetic properties, as well as aggregate stability in solutions of indifferent electrolyte (NaCl) in a wide pH range was studied. It has been found that a higher degree of purification of the samples and an increase in the number of protonated carboxyl groups on the surface of the DND particles due to additional acid and thermoammonia treatment leads to a shift in the position of the isoelectric point (IET) from pH 7.0 for the initial sample to pH 6.3 and pH 6.0, respectively. It is shown that the coagulation thresholds of hydrosols at natural pH and the position of stability zones in 10–3 M sodium chloride solution are in full compliance with the IET values. The highest thresholds are observed at pH 5.8 for the initial DND, while for the dispersion of DND particles after thermoammonia treatment, fast coagulation occurs already at a concentration of 10–4 M. It is also shown that the aggregate stability zones for additionally treated DND samples almost coincide. In the case of DND of basic purification, the stability zone expands in the area of positive zeta-potential, and in the area of negative values stability is not observed, probably due to the partial dissolution of surface impurities at high pH and their transition in ionic form to the solution, which causes coagulation of DND particles.



Electroconvection near two-layer composite microparticles
Abstract
This paper presents the results of a numerical simulation of an electrolyte solution behavior near a spherical dielectric microparticle covered with a homogeneous ion-selective shell under the influence of an external electric field. The particle is assumed to be stationary, and the electrolyte either stays still or is pumped externally with a constant velocity in absence of the electric field. The field, in turn, generates electroosmotic flow near the particle’s surface. It is shown that concentration polarization can occur near the particle, whereas electrokinetic instability only occurs near particles with a sufficiently thick shell. When the particle’s surface charge is opposite to the one of its shell, non-stationary regimes may be observed when the shell is thin enough.



Spherical polymer gels containing sulfonate groups: synthesis and adsorption properties
Abstract
Porous cross-linked polyelectrolyte microspheres with diameter from 1 to 5 μm based on para-styrene sulfonate or copolymer of para-styrene sulfonate with vinyl acetate were synthesized. The content of sulfonate groups in the obtained polyelectrolyte microspheres is more than 2 mmol/g. It was shown that introduction of hydrophobic comonomer significantly increased the degree of swelling of polyelectrolyte microspheres. It was found that the value of adsorption of model compounds (fuchsin, methylene blue) significantly exceed the concentration of sulfonate groups. Morphology, structure of the surface layer of polyelectrolyte matrices were studied by optical and scanning electron microscopy, FTIR spectroscopy, specific surface by the BET method.



Stabilization of bulk nanobubbles with a hydrate layer
Abstract
The stabilization of nanobubbles is considered with the balance of the Laplace pressure at their boundary due to surface tension and electrostatic pressure due to Coulomb forces. The presence of a hydrate layer of thickness ~1 nm with a tangential orientation of water dipoles around it is taken into account, the low permittivity of which, approximately equal to 3, increases the pressure at the nanobubble boundary. The sizes and charge of a stable nanobubble are determined. It is shown that in salt water, the hydration layer, regardless of the charge of the nanobubble, increases the pressure at its boundary by almost 30 times, and in fresh water - several times less.



Rheology of structured liquids. Flow regimes and rheological equations
Abstract
A system of rheological equations is presented, obtained on the basis of structural-kinetic representations, which describes viscous and elastic properties of structured liquids, namely concentrated suspensions, emulsions, micellar solutions, solutions and polymer melts. The structural model equations hold for equilibrium steady-state flow and for equilibrium oscillating flow. The equations are suitable for approximating rheological curves , , , , at individual intervals of shear rate or oscillation frequency. Each such interval corresponds to a certain state of the structure. As an example, the results of approximation of shear viscosity curves for polymer solution, micellar solution and emulsion are given.



Generation of latex particles and phase formation in a heterogeneous static monomer–water system
Abstract
The aim of this work is to find new ways to synthesize latexes (polymer suspensions) with a given size and surface structure of particles. The need for such latexes is not large-scale, but their development and production are extremely important for the development of high technologies. Monodisperse latexes are especially valuable in immunological diagnostics of a wide range of diseases. The article presents the results of studies of the nucleation of latex particles in a heterogeneous monomer–water system. The results of these studies made it possible to find conditions for the reproducible synthesis of monodisperse polystyrene latexes. In order to change the surface structure of latex particles, cetyl alcohol was dissolved in the initial monomer phase (styrene). The article presents the results of electron microscopic studies of the synthesized latexes. Nano crystals of this alcohol are clearly visible on the surface of the latex particles. It is suggested that, in deep monomer conversions, the process of crystallization of cetyl alcohol begins in polymer-monomer particles.



Surface modifiers for reducing bacterial contamination in medicine and food industry
Abstract
Antibacterial coatings are used in the food and textile industries, in the construction industry, in biotechnology and medicine. The review considers the main types of coatings that prevent fouling with biomacromolecules and microorganisms: anti-adhesive, contact, release-based, multifunctional and intelligent (“smart”) coatings. For each type of coating, the most relevant and effective active substances and their mechanism of action are described. Despite the widespread use of anti-adhesive surfaces and contact coatings, they have many disadvantages that limit the scope of their application and reduce activity and durability. Numerous studies show that multifunctional and intelligent coatings have high potential for practical application and further research on their modification to obtain universal and cost-effective coatings. The main problem of the practical application of such surfaces is the imperfection of methods for assessing the stability and antibacterial properties of the coating in laboratory conditions.



Kinetics of interaction of Co–Cu melts with graphite and microstructure of forming metal-carbon compositions
Abstract
The time dependences of the contact angle and the wetted surface spot diameter were measured during the interaction of Co–Cu melts with copper contents of 20, 40 and 60 at. % with graphite at temperatures of 1390, 1440, 1490, 1540 and 1590°C. Wetting of graphite by Co–Cu melts does not occur under these conditions: the final contact angle for Co80–Cu20 is 95°, Co60–Cu40 is 110°, Co40–Cu60 is 100°. The final value of the diameter of the wetted surface spot increases somewhat. Metallographic analysis of the microstructure of Co–Cu–C composite materials obtained by contact alloying of Co–Cu melts with carbon showed the dependence of the morphology of the structural components and the phase composition of the samples on the copper content. Composite materials (Co–27%C–10%Cu) + (Co–32%C–62%Cu) + C and (Co–19%C–15%Cu) + (Co–25%C–72%Cu) + C, obtained by the interaction of Co–Cu melts with a copper content of 20, 40 at. % with graphite, have a macro-homogeneous structure.


