催化作用
热解
聚烯烃
化学工程
材料科学
脱氢
分解
聚合物
产量(工程)
石油化工
有机化学
沸石咪唑盐骨架
热分解
精细化工
纳米材料基催化剂
金属有机骨架
碳氢化合物
化学反应
烯烃纤维
化学
碳纤维
无机化学
焦炭
过程(计算)
作者
Guoping Lu,Xueping Zhang,Kai Xu,Chenhao Tan,Yamei Lin,Wenbin Yi,Kangkang Sun,Matthias Beller
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-11-06
卷期号:12 (45)
标识
DOI:10.1126/sciadv.aeh0938
摘要
The chemical recycling of polyolefins (PO) via pyrolysis offers a circular pathway for plastic waste management, yet industrial implementation remains hindered by high energy demands and poor product selectivity. Here, we report an Fe-catalyzed pyrolysis process that achieves 97% PO conversion and a 94% yield of C6 to C35 liquid hydrocarbons. By using a zeolitic imidazolate framework (ZIF)–derived, N-doped porous carbon-supported iron single-atom catalyst (Fe 1 @NC) in combination with a strategic temperature gradient control, we overcome traditional thermolysis limitations. The process was further demonstrated on a kilogram scale, supporting the practical scalability of this catalytic system. Mechanistic investigations reveal that the rate-determining step is an acid base–promoted dehydrogenation of the polymer backbone. Specifically, electronic synergy between the single iron centers and the carbon support stabilizes reactive carbocation intermediates, facilitating their rapid decomposition into high-value olefins and alkanes. These findings provide a scalable and highly efficient catalytic framework for the upcycling of plastic waste into liquid hydrocarbon fractions and chemical feedstocks.
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