Patterns of Degradation of Binary Mixtures of Ultrafine Fibers Based on Poly-(3-Hydroxybutyrate) and Polyvinylpyrrolidone Under the Action of Ozonolysis

To obtain data on the effects of ozonolysis on the structural and dynamic parameters of ultrafine fibers based on the binary compositions of poly-(3-hydroxybutyrate) (PHB) and polyvinylpyrrolidone (PVP) with varying ratios of polymer components ranging from 0/100 to 100/0 mass%, produced by electrospinning, a study was conducted. The morphology and structural–dynamic characteristics of the ultrafine fibers were examined. Comprehensive research was carried out, combining thermophysical measurements (DSC), dynamic measurements using an electron paramagnetic resonance (EPR) technique, scanning electron microscopy, and infrared spectroscopy. The influence of the mixture’s composition and ozonolysis on the degree of crystallinity of PHB and the molecular mobility of the TEMPO radical (tetramethylpiperidine-1-oxyl) in the amorphous regions of the PHB/PVP fiber material was demonstrated. The low-temperature maximum on the DSC thermograms provided information about the fraction of hydrogen bonds in the mixed compositions, allowing for the enthalpy of thermal destruction of these bonds in both the original and oxidized samples to be determined. The study showed significant changes in the degree of crystallinity of PHB, the enthalpy of hydrogen bond destruction, molecular mobility, moisture absorption of the compositions, and the activation energy of rotational diffusion in the amorphous regions of the PHB/PVP mixed compositions. It was established that within the 50/50% PHB/PVP ratio, an inversion transition occurs from the dispersion material to the dispersion medium. Ozonolysis induces a sharp change in the material’s structure. The conducted research provided the first opportunity to assess the impact of ozonolysis on the structural and dynamic characteristics of PHB/PVP ultrafine fibers at a molecular level. These materials may serve as a therapeutic system for controlled drug delivery.