解聚
聚酯纤维
聚合物
生物复合材料
纤维小体
咪唑酯
挤压
化学
材料科学
生物催化
降级(电信)
基质(水族馆)
化学工程
水解
可生物降解聚合物
高分子
有机化学
生物降解
聚苯乙烯
高分子化学
漆酶
聚羟基丁酸酯
催化作用
聚合物降解
聚-3-羟基丁酸酯
酶
纤维素酶
颗粒
去肽
反应挤出
酶水解
作者
Shitong Cui,Jing Tian,Mengyu Zhu,Z B Liu,Yufei Cao,Yu Liu,Yuxiao Feng,Wanghui Xu,Weijian Lai,Hongyi Yang,J H Xu,Baohua Guo,Lin Qiu,Zhenzhong Yang,Paolo Falcaro,Jun Ge
摘要
ABSTRACT Controlling biocatalytic activity in melt‐processed polymers is a central challenge for triggered depolymerization, because enzymes deactivate at melt‐extrusion temperatures. Here, metal–organic framework‐gated biocatalysis, achieved by encapsulating enzymes within zeolitic imidazolate framework‐8 (ZIF‐8), preserves > 85% activity after 2 min at 180°C while regulating substrate access. Enzyme@ZIF‐8 biocomposite production scales to ∼50 kg day − 1 and is compounded by twin‐screw extrusion into poly(ε‐caprolactone) (PCL), poly(butylene adipate‐co‐terephthalate) (PBAT), and polylactide (PLA) at a tonne‐per‐day scale; pellets are compatible with standard thermoforming. The enzyme@ZIF/plastic composites retain mechanical performance comparable to the neat polymers during processing and use. At the end‐of‐life, chemical triggers dissolve the ZIF‐8 gate, releasing the enzyme, Zn 2 + and imidazolate to cooperatively accelerate depolymerization. Degradation increases 13.3–62.8‐fold for PCL and PLA in water and 1.7‐fold under industrial composting for PBAT and enables anaerobic PBAT digestion, whereas pristine polyesters show negligible conversion. This melt‐processable platform establishes gated, on‐demand depolymerization compatible with industrial polymer manufacturing.
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