Erasov V.S.

Candidate of Chemical Sciences (Ph.D.), Lecturer, Lomonosov Institute of Fine Chemical Technologies, MIREA – Russian Technological University

Surface modification of silica and titanium dioxide powders with silver nano- and microparticles by a thermal method

https://doi.org/10.58224/2619-0575-2026-9-2-2
Abstract
Objectives: to modify silica powder synthesized by the sol–gel method and commercial titanium dioxide with silver particles via thermal decomposition of silver nitrate within oxide matrices. To carry out a comparative study of the morphology and distribution of silver on different supports in terms of their potential application in photocatalysis and as functional abrasive fillers in toothpastes. To determine the nanostructure and specific surface area of silica and to assess the influence of the porous structure of the support on the dispersion of the silver phase.
Methods. Silica was obtained by sol–gel synthesis based on tetraethoxysilane. Modification of titanium dioxide and silica with silver was performed by impregnation with a silver nitrate solution followed by thermal decomposition of the salt at 700 °C. The morphology and distribution of silver were investigated by scanning electron microscopy and energy-dispersive elemental analysis with mapping. The nanostructure and porosity of silica were characterized by Sears titration and methylene blue adsorption with calculation of Langmuir equation constants and specific surface area.
Results. It was shown that commercial titanium dioxide consists of coarse particles (medium size 35,4 µm), whereas the sol–gel synthesized silica has the form of microspheres with medium size 1,4 µm and is composed of primary nanoparticles of about ~3.7 nm. According to methylene blue adsorption data, the specific surface area of silica is about 10 m²/g, which corresponds to a mesoporous structure. It was found that, upon modification of titanium dioxide with silver, submicron and micron-sized silver particles (up to ~2 µm) are formed on its surface, whereas on mesoporous silica a more highly dispersed silver phase is produced, which is not size-resolvable in SEM mode but is uniformly distributed over the surface according to EDS mapping data.
Conclusions. The morphology of the silver phase strongly depends on the type and structure of the oxide support. Mesoporous nanostructured silica promotes the formation of more highly dispersed (nanosized) and uniformly distributed silver particles compared to commercial titanium dioxide, on the surface of which submicron and micron silver inclusions prevail. The obtained data can be used to optimize the photocatalytic and antibacterial properties of silver-containing composites, as well as to select the composition of abrasive fillers based on SiO₂@Ag and TiO₂@Ag for toothpastes and other oral hygiene products.
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Colloidal protection of magnetite hydrosols with polysaccharides

https://doi.org/10.58224/2619-0575-2025-8-3-2
Abstract
This article investigates the stabilization of aqueous dispersions of magnetic Fe₃O₄ nanoparticles using polysaccharide stabilizers. The effect of electrolyte coagulants and polysaccharide stabilizers on the stability of magnetite hydrosols and their stability at physiological pH with and without the addition of polysaccharides is stud-ied. The results demonstrate the effectiveness of nonionic polysaccharides, such as hydroxypropyl methylcellulose and hydroxyethylcellulose, in stabilizing magnetic nanoparticles from electrolyte coagulation and over time, which is important for their application in medicine.
Objectives. To obtain and characterize magnetite hydrosols and to study their stabilization with polysaccharides over time and with the addition of non-indifferent and indifferent electrolytes.
Methods. Hydrosol coagulation was studied photometrically. The size of hydrosol nanoparticles was determined using dynamic light scattering.
Results. Nonionic polysaccharides, such as hydroxyethyl cellulose and hydroxypropyl methylcellulose, are promising for stabilizing aqueous dispersions (hydrosols) of Fe3O4 magnetic nanoparticles.
Conclusions. The coagulation threshold of magnetite hydrosol with a non-differentiated electrolyte, sodium hy-droxide, is 20,5 times lower than the coagulation threshold of magnetite hydrosol with an indifferent electrolyte, sodium chloride. Hydroxyethyl cellulose and hydroxypropyl methylcellulose exhibited the greatest protection of magnetite hydrosol from coagulation with sodium chloride. Hydroxypropyl methylcellulose exhibited the greatest protection of magnetite hydrosol from coagulation with sodium hydroxide. Sols containing hydroxypropyl methyl-cellulose exhibit the greatest stability over time at pH 7.4 (the pH of blood), created by the addition of a phosphate-buffered saline mixture.
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Surface-active and micelle-forming properties of binary mixtures of glycyrrhizin and decyl glycoside and stabilization of foam stabilized by such a mixture with xanthan and keratin additives

Abstract
The surface and micelle-forming properties of two surface-active sugar derivatives and their binary mixtures were studied: dipotassium glycyrrhizinate, which is an anionic surfactant of natural origin (saponin) and has biologically active properties, and a nonionic sugar surfactant decyl glycoside. Decyl glycoside has a noticeably higher surface activity and a noticeably lower CMC value than dipotassium glycyrrhizinate. Using Rubin's equations, the composition of mixed micelles and the parameters of surfactant interaction in them were calculated. It has been shown that a synergistic effect is observed in aqueous solutions of binary mixtures of these surfactants. Due to this, dipotassium glycyrrhizinate can be used together with decyl glycoside as a base for foaming solutions for cosmetic, pharmaceutical and medical foams. Using dispersion analysis of foam over time, the stability of foam stabilized with a mixture of dipotassium glycyrrhizinate and decyl glycoside in a molar ratio of 0.2:0.8 and the ef-fect on the stability of foam of the addition of two different biopolymers: polysaccharide - xanthan (xanthan gum) and protein - keratin of sheep wool hydrolyzate were studied. Based on dispersion analysis of foam micrographs, it was shown that both polymers increase the durability of the foam over time. Foam containing xanthan breaks down primarily through Ostwald ripening rather than coalescence. Foam with keratin hydrolyzate has a lower initial dispersion and number of bubbles than foam with keratin hydrolyzate. The stability of both foams is close, but slightly higher in the case of the addition of keratin.
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Adsorption of kappa-carrageenan on the surface of chitosan and its sulfuric acid salt and stabilization of chitosan-sulfate nanoparticles by it

Abstract
Objectives: to investigate the adsorption of k-carrageenan on the surface of chitosan at pH 7.4 and chitosan treated with dilute sulfuric acid solution (pH 2.5-2.7). To develop a method for obtaining the sol of the chitosan sulfate salt - chitosan sulfate (CX) and to investigate its stability in time depending on the use of various acids as precursors, and its increase with the addition of different concentrations of k–carrageenan.
Methods. To determine the viscosity of polymer solutions, their molecular weight and to study the adsorption of k-carrageenan on CX, the method of capillary viscometry was used. The assessment of the stability of the zones over time was carried out photometrically.
Results. The adsorption of k-carrageenan on chitosan and CX has been studied: experimental isotherms of k-carrageenan adsorption have been constructed.on the surfaces of chitosan and CX, the constants of the Langmuir equation are calculated and complete theoretical adsorption isotherms are constructed using them. A method for obtaining a CX hydrosol with a positive particle charge has been developed. The stability of CX sols in time both without additives and with additives of k-carrageenan in time has been studied.
Conclusions. The adsorption of k-carrageenan on chitosan and CX is monomolecular. The adsorption equilibrium constant is greater with the adsorption of k-carrageenan on the surface of CX, and the maximum adsorption value is greater with the adsorption on the surface of chitosan. Of the acids used as precursors, the sol obtained using citric acid has the greatest stability. With an additional additive to the sols of the protective colloid - k-carrageenan to sols obtained using hydrochloric acid and citric acid, the sol obtained with the use of hydrochloric acid and carrageenan additives in the range of 0.04-0.06% has the greatest aggregate stability.
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