The hydrolytic and enzymatic degradation of polymer films of poly(3-hydroxybutyrate) (PHB) of different molecular mass and its copolymers with 3-hydroxyvalerate (PHBV) of different 3-hydroxyvalerate (3-HV) content and molecular mass, 3-hydroxy-4-methylvalerate (PHB4MV), and polyethylene glycol (PHBV-PEG) produced by the Azotobacter chroococcum 7B by controlled biosynthesis technique were studied under in vitro model conditions. The changes in the physicochemical properties of the polymers during their in vitro degradation in the pancreatic lipase solution and in phosphate-buffered saline for a long time (183 days) were investigated using different analytical techniques. A mathematical model was used to analyze the kinetics of hydrolytic degradation of poly(3-hydroxyaklannoate)s by not autocatalytic and autocatalytic hydrolysis mechanisms. It was also shown that the degree of crystallinity of some polymers changes differently during degradation in vitro. The total mass of the films decreased slightly up to 8–9% (for the high-molecular weight PHBV with the 3-HV content 17.6% and 9%), in contrast to the copolymer molecular mass, the decrease of which reached 80%. The contact angle for all copolymers after the enzymatic degradation decreased by an average value of 23% compared to 17% after the hydrolytic degradation. Young’s modulus increased up to 2-fold. It was shown that the effect of autocatalysis was observed during enzymatic degradation, while autocatalysis was not available during hydrolytic degradation. During hydrolytic and enzymatic degradation in vitro, it was found that PHBV, containing 5.7–5.9 mol.% 3-HV and having about 50% crystallinity degree, presents critical content, beyond which the structural and mechanical properties of the copolymer have essentially changed. The obtained results could be applicable to biomedical polymer systems and food packaging materials.

In our study, we investigated the accelerated aging process of PLA under 253.7 nm UV-C irradiation with the use of the GPC, NMR, FTIR, and DSC methods and formal kinetic analysis. The results of GPC and DSC indicated a significant degree of destructive changes in the PLA macromolecules, while spectroscopic methods NMR and FTIR showed maintenance of the PLA main structural elements even after a long time of UV exposure. In addition to that, the GPC method displayed the formation of a high molecular weight fraction starting from 24 h of irradiation, and an increase in its content after 144 h of irradiation. It has been shown for the first time that a distinctive feature of prolonged UV exposure is the occurrence of intra- and intermolecular radical recombination reactions, leading to the formation of a high molecular weight fraction of PLA decomposition products. This causes the observed slowdown of the photolysis process. It was concluded that photolysis of PLA is a complex physicochemical process, the mechanism of which depends on morphological changes in the solid phase of the polymer under UV radiation.

Compositions of polylactide (PLA) and poly(3-hydroxybutyrate) (PHB) thermoplastic polyesters originated from the nature raw have been obtained by blending under shear deformations and electrospinning methods in the form of films and nanofibers as well as unwoven nanofibrous materials, respectively. The degrees of crystallinity calculated on the base of melting enthalpies and thermal transition temperatures for glassy state, cold crystallization, and melting point for individual biopolymers and ternary polymer blends PLA-PHB- poly(ethyleneglycol) (PEG) have been evaluated. It has been shown that the mechanical properties of compositions depend on the presence of plasticizers PEG with different molar masses in interval of 400–1000. The experiments on the action of mold fungi on the films have shown that PHB is a fully biodegradable polymer unlike PLA, whereas the biodegradability of the obtained composites is determined by their composition. The sorption activity of PLA–PHB nanofibers and unwoven nanofibrous PLA–PHB composites relative to water and oil has been studied and the possibility of their use as absorbents in wastewater treatment from petroleum products has been demonstrated.

The main problems of remote sensing of the Earth’s surface within the frequency range 1.2–1.6 GHz are discussed. They are related to the resonant quantum properties of the radio wave propagation medium in the lower ionosphere. It is shown that, for the passive remote sensing, the main source is incoherent microwave radiation of the D and E ionospheric layers in the decimeter range. For the first time, a theoretically grounded principally new scheme of measurements is suggested. The scheme assumes that the radiation source exists below the satellite orbit and accounts for the fact that two types of radiation (direct and reflected) reach the satellite sensor. The separation of the respective fluxes is a serious problem that should be solved for the correct interpretation of the measurements. The question is raised regarding the correct calibration of measuring equipment, depending on the current state of the ionosphere.

An epoxy resin modified with polysulfone (PSU) and active diluent furfuryl glycidyl ether (FGE) was studied. Triethanolaminotitanate (TEAT) and iso-methyltetrahydrophthalic anhydride (iso-MTHPA) were used as curing agents. It is shown that during the curing of initially homogeneous mixtures, heterogeneous structures are formed. The type of these structures depends on the concentration of active diluent and the type of hardener. The physico-mechanical properties of the hybrid matrices are determined by the structure formed. The maximum resistance to a growing crack is provided by structures with a thermoplastic-enriched matrix-interpenetrating structures. The main mechanism for increasing the energy of crack propagation is associated with the implementation of microplasticity of extended phases enriched in polysulfone and their involvement in the fracture process.

The review considers the current ideas of a relatively new field of "green chemistry" in the field of chemical processing of renewable natural plant raw materials. For a number of processes, the ways, methods and some technological aspects of obtaining new compounds and reagent systems, biodegradable compositions and "green chemistry" products that are in demand in various sectors of the economy, industry and life support of society are shown. The article presents the results of the analysis of Russian and world reserves of forest resources according to authoritative modern sources and proposals for their conservation and restora-tion. The problems of biorefiling of plant raw materials are described, one of which is the val-orization of lignin-the aromatic component of the chemical composition of wood. It is pro-posed to obtain biodegradable systems and compositions based on the by-product of wood processing lignosulfonate of a neutral production method characterized by a high content of polysaccharides in the hemicellulose of the carbohydrate part of wood after the separation of cellulose. The ways of using modified cellulose products as inhibitors of salt deposition and gas hydrate formation, and the areas of their application in oilfield chemistry are shown. Lig-nin and other components of plant resources have long been the basis of various classes of fi-bers of natural origin, including plant and animal origin, artificial fibers. In the sector of cre-ating materials with new properties that have a wide range of practical applications, the review describes the production of PLA polylactide synthesized from lactic acid as a modern alterna-tive to many synthetic polymers obtained from refined petroleum products. For the products of the interaction of ammonium lactate and N-butyl alcohol, a kinetic model for the production of butyl lactate, an intermediate product of green chemistry, is described. The results of the study of a specific class of compounds – ionic liquids – traditionally considered as so-called "green solvents" are presented. An approach to the creation of a mathematical model by calculating the adsorption characteristics for evaluating the effectiveness of systems and composites based on biodegradable polymers in the direction of "green chemistry" is proposed.