In an environment of high salinity, low temperature, and the presence of a few bacteria in seawater, improving the non-enzymatic hydrolysis of polyesters is one of the effective methods for developing seawater degradable materials. In this research, poly­(butylene furandicarboxylate-co-glycolate) (PBFGA) copolyesters were synthesized via melt polycondensation. The PBFGA copolymer possessed excellent mechanical properties and thermal stability. Its tensile strength was 15–50 MPa and the elongation at break was more than 120% from the tensile tests. GA units improved the flexibility of PBF segments, and the PBFGA copolymer exhibited an amorphous structure. The PBFGA copolymer possessed good hydrolysis properties and the weight loss of PBFGA50 was more than 30% after 84 days of degradation in deionized water. Lipase catalyzed, and the salt inhibited the hydrolysis of the ester bond. PBFGA exhibited a bulk degradation mechanism, and sponge pores were formed on the surface due to preferential degradation of the PGA component, which was conducive to the further degradation of the internal groups. Some butanediol and glycolic acid terminated oligomers were produced during the degradation process, and rearrangement crystallization occurred in the chain segment. Thus, PBFGA copolyesters have the potential to serve as promising seawater degradable materials with excellent tensile and non-enzymatic degradable properties.

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In response to the shortage of fossil fuels, efficient electrochemical energy conversion devices are attracting increasing attentions while a daunting challenge regarding the limited electrochemical performance and high cost of...

Biodegradable nanocomposites were prepared by melt blending biodegradable poly(lactic acid) (PLA) and poly(butylene adipate-co-butylene terephthalate) (PBAT) (70/30, w/w) with diatomite or talc (1–7%). From the SEM test, the particles were transported to the interface of two phases, which acted as an interface modifier to strengthen the interfacial adhesion between PLA and PBAT. Talc and diatomite acted as nucleating agents to improve the crystallization of PBAT in the blends by DSC analysis. Moreover, adding the particles improved the tensile and impact toughness of the blends. The elongation at break with 5% talc was 78% (vs ∼21%) and the impact strength was 15 kJ/m2 (vs ∼6.5 kJ/m2). The rheological measurement revealed that the talc and diatomite reduced the viscosity of the blends. The results showed a good possibility of using talc- and diatomite-filled PLA/PBAT blends with high toughness for green-packaging and bio-membranes application.