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用于塑料解聚的金属有机框架催化剂。

MOF Catalysts for Plastic Depolymerization.

作者信息

Nguyen Bao-Nguyen T, Tan Tristan T Y, Otake Ken-Ichi, Kitagawa Susumu, Lim Jason Y C

机构信息

Laboratory of Green Porous Materials, Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology and Research (A*STAR), 2 Fusionopolis Way, Innovis #08-03, Singapore, 138634, Republic of Singapore.

Institute for Integrated Cell-Material Sciences, Kyoto University Institute for Advanced Study, Kyoto University Yoshida, Ushinomiya-cho, Sakyo-ku, Kyoto, 606-8501, Japan.

出版信息

Angew Chem Int Ed Engl. 2025 Jun 17;64(25):e202504017. doi: 10.1002/anie.202504017. Epub 2025 May 8.

DOI:10.1002/anie.202504017
PMID:40302236
Abstract

Depolymerization is a promising solution to address the escalating global plastic waste crisis, as a key enabler for emerging technologies in chemical upcycling and closed-loop recycling of plastics. By virtue of their unparalleled bottom-up designability for structural control, stability, reactivity, and compatibility with catalytically-active metal nanoparticles and enzymes, MOFs have enormous potential as an emerging class of porous heterogeneous catalysts for plastics depolymerization. Herein, we highlight key considerations and advances in MOF catalyst development and design for a range of depolymerization reactions, including alcoholysis, hydrogenolysis, pyrolysis, photocatalytic oxidation, and enzymatic hydrolysis. Other than enabling MOFs to efficiently depolymerize the most abundant plastics in production today, including those with unreacted C─C backbones (e.g., polyolefins) and polymers with cleavable backbone linkages (e.g., polyesters), their versatility also extends to emerging applications in microplastic capture and degradation from wastewater. These unique properties of MOFs position them as potentially scalable and reusable heterogeneous catalysts that can complement existing inorganic catalysts for practical depolymerization.

摘要

解聚是解决全球塑料垃圾危机不断升级的一个有前景的解决方案,是塑料化学升级循环和闭环回收等新兴技术的关键推动因素。由于金属有机框架材料(MOFs)在结构控制、稳定性、反应活性以及与催化活性金属纳米颗粒和酶的兼容性方面具有无与伦比的自下而上的可设计性,它们作为一类新兴的用于塑料解聚的多孔多相催化剂具有巨大潜力。在此,我们重点介绍了MOF催化剂在一系列解聚反应(包括醇解、氢解、热解、光催化氧化和酶促水解)的开发和设计中的关键考虑因素和进展。MOFs不仅能够有效地解聚当今生产中最常见的塑料,包括那些具有未反应碳 - 碳主链的塑料(如聚烯烃)和具有可裂解主链键的聚合物(如聚酯),其多功能性还扩展到从废水中捕获和降解微塑料的新兴应用。MOFs的这些独特性质使其成为潜在的可扩展和可重复使用的多相催化剂,可补充现有的无机催化剂用于实际解聚。

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