Publications by authors named "Gennady P Kopitsa"

Article Synopsis
  • Ionogels were created by mixing Aerosil A380 with varying amounts (16.3 to 79.9 mol %) of a specific ionic liquid, 1-methyl-3-octyl-imidazolium tetrafluoroborate (OMIM BF).
  • Evidence of changes in the ionic liquid's behavior was observed through NMR and IR spectroscopy, indicating that the liquid was confined within the silica structure, which also affected its decomposition temperature.
  • Structural analysis revealed that the ionic liquid filled different pore sizes in the Aerosil, with notable increases in size correlations in higher IL content; this suggests that altering IL concentrations can modulate the material's properties effectively.
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A series of silica-based aerogels comprising novel bifunctional chelating ligands was prepared. To produce target aerogels, two aminosilanes, namely (3-aminopropyl)trimethoxysilane (APTMS) and -(2-aminoethyl)-3-aminopropyltrimethoxysilane (AEAPTMS), were acylated by natural amino acids (()-(+)-2-phenylglycine or -phenylalanine), followed by gelation and supercritical drying (SCD). Lithium tetrachloropalladate was used as the metal ion source to prepare strong complexes of Pd with amino acids covalently bonded to a silica matrix.

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New composite hydrogels (CH) based on bacterial cellulose (BC) and poly-1-vinyl-1,2,4-triazole (PVT) doped with orthophosphoric acid (oPA), presenting interpenetrating polymeric networks (IPN), have been synthesized. The mesoscopic study of the supramolecular structure (SMS) of both native cellulose, produced by the strain , and the CH based on BC and containing PVT/oPA complex were carried out in a wide range of momentum transfer using ultra- and classical small-angle neutron scattering techniques. The two SMS hierarchical levels were revealed from 1.

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The chemical immobilization of cobalt(II) ions in a silica aerogel matrix enabled the synthesis of the first representative example of aerogel-based single-ion magnets. For the synthesis of the lyogels, methyl-trimethoxysilane and N-3-(trimethoxysilyl)propyl ethylenediamine were co-hydrolyzed, then the ethylenediamine groups that were immobilized on the silica matrix enabled the subsequent binding of cobalt(II) ions. Lyogels with various amounts of ethylenediamine moieties (0.

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A series of multiblock polyurethane-ureas (PUU) based on polycaprolactone diol (PCL) with a molecular mass of 530 or 2000 g/mol, as well as hard segments of different lengths and structures, were synthesized by the step-growth polymerization method. The chemical structure of the synthesized multiblock copolymers was confirmed by IR- and NMR-spectroscopy. Differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) were used to determine the relaxation and phase transition temperatures for the entire series of the obtained PUU.

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Microbially induced CaCO precipitation (MICP) is considered as an alternative green technology for cement self-healing and a basis for the development of new biomaterials. However, some issues about the role of bacteria in the induction of biogenic CaCO crystal nucleation, growth and aggregation are still debatable. Our aims were to screen for ureolytic calcifying microorganisms and analyze their MICP abilities during their growth in urea-supplemented and urea-deficient media.

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Article Synopsis
  • Ceric hydrogen phosphate gels have a unique fibrous and nearly amorphous structure, making them special materials.
  • Researchers used a sol-gel method to create gels that can hold up to 20,000 water molecules for each cerium atom.
  • Supercritical processing of these gels led to the development of ultralight aerogels that are noncarbonaceous and have an extremely low density of just 1 mg/cm³.
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The crystal and supramolecular structure of the bacterial cellulose (BC) has been studied at different stages of cellobiohydrolase hydrolysis using various physical and microscopic methods. Enzymatic hydrolysis significantly affected the crystal and supramolecular structure of native BC, in which the 3D polymer network consisted of nanoribbons with a thickness ≈ 8 nm and a width ≈ 50 nm, and with a developed specific surface ≈ 260 m·g. Biodegradation for 24 h led to a ten percent decrease in the mean crystal size of BC, to two-fold increase in the sizes of nanoribbons, and in the specific surface area up to ≈ 100 m·g.

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Tungsten oxide-based bulk and nanocrystalline materials are widely used as photocatalytic and photo- and electrochromic materials, as well as materials for biomedical applications. In our work, we focused our attention on the effect of sodium cations on the structure and photochromic properties of the WO@PVP aqueous sols. To establish the effect, the sols were synthesized by either simple pH adjusting of sodium or ammonium tungstates' solutions, or using an ion exchange technique to remove the cations from the materials to the greatest possible extent.

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Spherical nanoparticles of ZrO with 2 and 10 mol% EuO up to 20 nm size were prepared by the method of hydrothermal synthesis for luminescent functionalization of the polymer-inorganic nanocomposites based on poly(methyl methacrylate). Surface modification of oxide nanoparticles was carried out by 3-(trimethoxysilyl)propyl methacrylate, dimethoxymethylvinyl silane and 2-hydroxyethyl methacrylate to provide uniform distribution and to prevent agglomeration of nanosized filler in the polymer matrix. Polymer-inorganic composites were synthesized by in situ free radical polymerization in bulk.

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