Biodegradable polymers are getting attention as renewable alternatives to petroleum-based plastics due to their environmental benefits. However, improving their physical properties remains challenging. In this work, biodegradable biopolymers (PVA-PCD) were fabricated by chemically crosslinking petroleum-based polyvinyl alcohol (PVA) with biomass-derived cardanol-based polyols (PCD). Biopolymers were characterized using various techniques, including Fourier-transform infrared (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and swelling tests. Cardanol, the raw material, was converted into polyols via epoxidation followed by hydroxylation. FT-IR analysis confirmed that PVA-PCD biopolymers were crosslinked between the hydroxyl groups of PVA and PCD and the aldehydes of crosslinker glutaraldehyde (GLU), accompanied by the formation of acetal groups with ether bridges. XRD showed that the crystallinity of crosslinked polymers decreased, indicating that crosslinking occurs disorderly. TGA exhibited that GLU significantly improved the thermal stabilities of PVA and PCD-PVA polymers, as evidenced by increased decomposition temperatures. On the other hand, the effect of PVA/PCD ratios was minor on biopolymers’ thermal stabilities. Swelling tests revealed that increased crosslinking density decreased the swelling ratio, suggesting that PVA-PCD biopolymers become more hydrophobic with high brittleness, high strength, and low swelling capacity. In summary, this study demonstrates that PVA-PCD biopolymers fabricated from biomass-derived materials have potential for various applications, such as biodegradable materials and sustainable packaging.

Marine biomass has attracted attention as an environmentally sustainable energy source that can replace petroleum-based resources. Alginates, the main natural polysaccharides extracted from seaweeds, are used in various fields, such as food, pharmaceuticals, and chemical raw materials. Because the versatile applications of alginates depend on their physicochemical properties, which are controlled by their molecular weights, proper alginate depolymerization should be established. Previous approaches have limitations such as long reaction times and environmental issues. In this study, we report eco-friendly alginate depolymerization using hydrogen peroxide (H₂O₂)-induced oxidative decomposition and high-frequency ultrasonication. In oxidative decomposition, the depolymerization tendency depends on both the temperature and the use of iron oxide catalysts that can promote the Fenton reaction. Ultrasonication is effective in promoting selective depolymerization and ring-opening reactions. Oligo-alginates obtained through the precise molecular weight regulation of alginate offer potential applications in medical devices and platform chemicals.