Biomaterials (films, foils, fibers, coatings) based on proteins are becoming increasingly important due to the growing applications for which pork and beef gelatins are used. Alternative types of gelatins (poultry or fish), which have not yet been sufficiently tested, represent a high potential. This study looks at the effect of different UV exposure times on chicken gelatin films with added glycerol. The gelatin was prepared using a unique enzymatic hydrolysis process. The quality of the UV-exposed films was compared with gelatin films not exposed to UV light. Radiation-induced crosslinking improved the mechanical and physical properties of the films. The UV crosslinked films are stabilized at a degree of swelling from 700 to 900%; moreover, they extend their dissolution to more than 7 days while maintaining their original shape. In contrast, non-crosslinked films swell and dissolve in water faster. Further, the effect of UV radiation on the water vapor permeability and color of the films was monitored. Water vapor permeability decreased by 2.5 times with increasing crosslinking time for 30% and 40% glycerol content, and the yellowness of the irradiated samples increased with exposure time in the interval from 24 to 28. Using Fourier transform infrared spectroscopy, the differences in the amount of bonding based on irradiation time were analyzed. As a result of crosslinking, the intensity of existing bonds increased. Thermal properties were verified through differential scanning calorimetry and thermogravimetric analysis. The results proved that chicken gelatin is suitable for preparing films in foods and medicine. Applying UV radiation to crosslink gelatin films is an alternative to traditionally used chemical crosslinkers.

This study examines binary blends of three types of polyhydroxyalkanoates (PHAs)—poly(3-hydroxybutyrate) (PHB), poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH), and poly(3-hydroxybutyrate-co-4-hydroxybutyrate) (P3HB4HB)—with a focus on their rheological, thermal, and mechanical behavior. The blends exhibit partial miscibility in both the melt and solid states. Glass transition analysis revealed that semicrystalline/amorphous PHA combinations are fully miscible (single Tg) at amorphous PHA contents below 30 wt%. Above this threshold, a two-phase morphology develops, consisting of crystalline spherulites embedded in an amorphous matrix. When the amorphous PHA content reached ≥30 wt%, the blends could be oriented by stretching, yielding materials that display thermoplastic elastomer (TPE)-like behavior without chemical modification of the base polymers. Thermal and mechanical characterization, supported by X-ray diffraction of samples before and after orientation, confirmed that the elastomeric properties originate from the multiphase architecture formed by crystalline and amorphous domains interconnected through a miscible amorphous fraction.

In this work, we examined the degradation behavior of isotactic poly(1-butene) (PB-1) under artificial aging and natural weathering conditions. PB-1 samples underwent accelerated aging through UV irradiation and natural weathering. Chemical and structural changes in the degraded samples were characterized using Fourier-transform infrared–attenuated total reflectance (FTIR–ATR) spectroscopy, surface analysis, and wide-angle X-ray scattering (WAXS). The mechanical properties were evaluated via tensile testing. FTIR–ATR analysis revealed the presence of carbonyl groups in the degraded samples, indicating oxidative degradation. Surface observations employing scanning electron microscopy (SEM) revealed the formation of surface cracks in both samples, with differing crack initiation mechanisms. The two aging methods affected the mechanical properties of the samples: artificial aging induced a gradual reduction in both tensile modulus and strength, whereas natural weathering engendered a marginal increment in modulus alongside diminished strength. Additionally, elongation-at-break value witnessed a marked decrease in both sample sets during the preliminary stages of degradation. This work employed accelerated time equivalent, obtained by juxtaposition of the values of carbonyl index during both artificial aging and natural weathering and their interpolation to determine the degradation rate and adequately to correlate the final properties of the aged PB-1. It was observed that surface morphology and mechanical attributes of degraded samples were subject to additional influences such as temperature, humidity, and precipitation during natural weathering. This research work provided significant insights into PB-1 degradation mechanisms and effect of different aging conditions on its performance. Graphical abstract