Synthesis of renewable and seawater-degradable polyesters based on a fully biobased diester

• Fully biobased monomer PBPC with two pyrrolidone rings was synthesized from renewable 1,5-pentanediamine and dimethyl itaconate . • The polyesters with high molecular weight derived from PBPC exhibited rapid seawater-degradability. • The homopolyesters incorporated PBPC showed remarkable UV shielding abilities compared with poly(lactic acid) (PLA) and poly(butylene succinate) (PBS). • The introduction of PBPC into poly(butylene terephthalate) (PBT) resulted in the elevated toughness. The design and development of biobased plastics that can degrade in seawater is a potential approach to address the seawater pollution of fossil plastics. Herein, N,N '-pentamethylene-bis(pyrrolidone-4-methyl carboxylate) (PBPC), a biobased diester with two pyrrolidone rings, was synthesized from renewable 1,5-pentanediamine and dimethyl itaconate. PBPC was polymerized with three α,ω-diols to prepare biobased homopolyesters with number-average molecular weight ( M n ) around 25 kDa. These amorphous homopolyesters presented remarkable UV shielding abilities compared with poly(lactic acid) (PLA) and poly(butylene succinate) (PBS). Incubation experiments in artificial seawater for 150 days indicated that the homopolyesters based on PBPC exhibited rapid seawater-degradability. Then, PBPC was copolymerized with 1,4-butanediol and terephthalic acid to prepare a series of copolyesters with M n around 20 kDa. The introduction of PBPC into poly(butylene terephthalate) (PBT) resulted in the elevated toughness and sensitivity to seawater degradation. Depending on the composition of PBPC, the thermal, mechanical, and degradation rate of the copolyesters were adjustable. Overall, the PBPC-based polyesters are promising alternatives to commercial packaging materials in improving the renewability of raw materials and achieving seawater degradation.