Journal
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 9, Issue 5, Pages 2280-2290Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c08274
Keywords
Biodegradable polyesters; Spiro diacetal; Switch of degradation; Acid degradation; Physicochemical properties
Categories
Funding
- National Key Research and Development Program of China [2017YFB0303000]
- National Natural Science Foundation of China [51773218]
- China Postdoctoral Science Foundation [2020M681963]
- Youth Innovation Promotion Association of CAS [2018338]
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By introducing acetal units into poly(butylene succinate), the biodegradation of copolyesters has been locked and unlocked, showing reliable stability and controlled degradation. Among them, PBSS65 exhibited excellent mechanical properties and stability, making it a promising candidate for future applications.
The gradual degradation of polyester in daily use causes unpredictable failure and restricts its reliable applications. The realization of excellent stability in use and controlled degradation in a specific environment is highly appreciated but still remains challengeable. Here, we demonstrate a new solution via introducing acetal units into poly(butylene succinate): locking the biodegradation of copolyesters by rigid Spiro diacetal, which could be unlocked in strong acidic circumstances. In detail, a series of poly(butylene succinate-co-spirocyclic succinate) (PBSS) copolyesters containing different contents of spiroglycol (SPG) were prepared and characterized. Among them PBSS65 behaved as an excellent candidate for future application, which possessed a high elastic modulus (1.87 GPa) and tensile strength (46 MPa) and moderate elongation at break (252%). It kept stable after melt processing and pH 0-14 soaking, showing solid reliability in daily use. Its biodegradation was locked by the steric hindrance effect of SPG units. Only after treatment in acetone/H2O mixed acidic solution could the biodegradation be triggered. Moreover, it was found that the prolongation of the acid treatment time could accelerate the biodegradation process. The controlled degradation mechanism was proposed to be consisted of acid cleavage of SPG unit and enzymatic degradation of ester group.
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