Aliphatic and aromatic polyesters of hydroxycarboxylic acids are characterized not only by biodegradability, but also by biocompatibility and inertness, which makes them suitable for use in different applications. Polyesters with high enzymatic hydrolysis capacity include poly(lactic acid), poly(ε-caprolactone), poly(butylene succinate) and poly(butylene adipate-co-terephthalate), poly(butylene succinate-co-adipate). At the same time, poly(lactic acid) is the most durable, widespread, and cheap polyester from this series. However, it has a number of drawbacks, such as high brittleness, narrow temperature-viscosity processing range, and limited biodegradability. Three main approaches are known for poly(lactic acid) modification: incorporation of dispersed particles or low molecular weight and oligomeric substances, copolymerization with other polymers, and blending with other polymers. The review includes an analysis of experimental works devoted to developing mixtures based on poly(lactic acid) and other polymers. Regularities in the formation of the structure of such systems and the possibility of controlling the properties of poly(lactic acid) are considered.

A review of data on the thermo, photo-, and biodegradation of compositions of synthetic polymers with poly-3-hydroxybutyrate and poly(lactic acid) is presented. The influence of these polymers on the...

In the work, the impact of the biological medium and water on structural rearrangements in pure polylactide and polylactide/natural rubber film composites was studied. Polylactide/natural rubber films with a rubber content of 5, 10, and 15 wt.% were obtained by the solution method. Biotic degradation was carried out according to the Sturm method at a temperature of 22 ± 2 °C. Hydrolytic degradation was studied at the same temperature in distilled water. The structural characteristics were controlled by thermophysical, optical, spectral, and diffraction methods. Optical microscopy revealed the surface erosion of all samples after exposure to microbiota and water. Differential scanning calorimetry showed a decrease in the degree of crystallinity of polylactide by 2–4% after the Sturm test, and a tendency to an increase in the degree of crystallinity after the action of water was noted. Changes in the chemical structure were shown in the spectra recorded by infrared spectroscopy. Due to degradation, significant changes in the intensities of the bands in the regions of 3500–2900 and 1700–1500 cm⁻¹ were shown. The X-ray diffraction method established differences in diffraction patterns in very defective and less damaged regions of polylactide composites. It was determined that pure polylactide hydrolyzed more readily under the action of distilled water than polylactide/natural rubber composites. Film composites were more rapidly subjected to biotic degradation. The degree of biodegradation of polylactide/natural rubber composites increased with the rise in the content of natural rubber in the compositions.

Lignosulfonate is a cheap material available in large quantities obtained as a byproduct of paper and cellulose. In this work, blends of polypropylene (PP) and sodium lignosulfonate (LGNa) were developed to evaluate the potential use of lignosulfonate as a lightweight, thermal insulation and flame retardant material. The blends were obtained by mixing in a torque rheometer and molded after compression. The blend proprieties were evaluated by physical, morphological, thermal, thermal conductivity, and flammability tests. The measured values were compared with theoretical models. The results indicated that a heterogeneous blend with a higher number of separated domains is formed when the LGNa content increases from 10 to 40 wt%. In addition, the density and thermal conductivity coefficient of the blends studied are not affected by the addition of LGNa. However, when the LGNa content in the blend exceeds 20 wt% the thermal stability and flame retardant proprieties are considerably reduced. The theoretical models based on the rule of mixtures showed a good agreement with the experimental values obtained from blend density, thermal conductivity, and thermal stability. In general, lignosulfonate tested in this work shows potential to be used as a reactive component in polymer blends.

Electrospun fabrics have unique properties due to their uniform morphology and high surface area to volume ratio. Ultrathin nonwoven fabrics are produced for many applications: biomedical, nanosensors, tissue engineering and filtration systems. In this work, nonwoven polylactide, polylactide/natural rubber, poly-3-hydroxybutyrate, and poly-3-hydroxybutyrate/nitrile butadiene rubber fabrics were prepared by electrospinning methods. The obtained fabric samples were used as substrates for the growth of winter wheat seeds “Yubileinaya 100” (Triticum aestivum L.). The stimulating effect of polymer substrates on seed germination and plant growth was shown. The structure and properties of nonwoven agromaterials were controlled by differential scanning calorimetry, IR-spectroscopy, and optical microscopy. The mechanical properties of the obtained fabrics before and after their utilization as substrates were studied. After the wheat growing experiment, the degree of crystallinity of PHB and PHB/NBR samples decreased by 12% and they completely lost their mechanical properties. It is shown that the main factors providing the efficiency of seed growth technology on polymer substrates are the chemical nature and structure of the biodegradable matrix.

The influence of physical factors on the destruction of biodegradable polymers is also important to evaluate, predicting the period of their full degradation in the environment. One of the most significant environmental factors is the ultraviolet radiation. The influence of UV radiation time on polylactide destruction was proved by infrared (IR) spectroscopy and differential scanning calorimetry (DSC).