弹性体
羟基烷酸
生物降解
共价键
材料科学
聚合物
高分子科学
纳米技术
化学
有机化学
复合材料
遗传学
细菌
生物
作者
Robin M. Cywar,Chen Ling,Ryan W. Clarke,Dong Hyun Kim,Colin M. Kneucker,Davinia Salvachúa,Bennett Addison,Sarah A. Hesse,Christopher J. Takacs,Shu Xu,Meltem Urgun Demirtas,Sean P. Woodworth,Nicholas A. Rorrer,Christopher W. Johnson,Christopher J. Tassone,Robert D. Allen,Eugene Y.‐X. Chen,Gregg T. Beckham
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-11-24
卷期号:9 (47)
被引量:5
标识
DOI:10.1126/sciadv.adi1735
摘要
Cross-linked elastomers are stretchable materials that typically are not recyclable or biodegradable. Medium-chain-length polyhydroxyalkanoates (mcl-PHAs) are soft and ductile, making these bio-based polymers good candidates for biodegradable elastomers. Elasticity is commonly imparted by a cross-linked network structure, and covalent adaptable networks have emerged as a solution to prepare recyclable thermosets via triggered rearrangement of dynamic covalent bonds. Here, we develop biodegradable and recyclable elastomers by chemically installing the covalent adaptable network within biologically produced mcl-PHAs. Specifically, an engineered strain of Pseudomonas putida was used to produce mcl-PHAs containing pendent terminal alkenes as chemical handles for postfunctionalization. Thiol-ene chemistry was used to incorporate boronic ester (BE) cross-links, resulting in PHA-based vitrimers. mcl-PHAs cross-linked with BE at low density (<6 mole %) affords a soft, elastomeric material that demonstrates thermal reprocessability, biodegradability, and denetworking at end of life. The mechanical properties show potential for applications including adhesives and soft, biodegradable robotics and electronics.
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