解耦(概率)
乙丙橡胶
聚乙烯
动能
乙烯
闭环
材料科学
化学
复合材料
物理
共聚物
催化作用
有机化学
经典力学
工程类
聚合物
控制工程
作者
Tianrui Bi,Yinlin Chen,Longfei Lin,Xue Han,Yang Pan,Chengyuan Liu,Z. H. Cen,Cong Luo,Weilong Wen,Hunain Zulfiqar,Xinrui Zheng,Pascal Manuel,Qian Li,Ningning Wu,Junfeng Xiang,Sihai Yang⧫,Buxing Han
标识
DOI:10.1038/s44286-025-00290-y
摘要
Abstract Conversion of polyethylene (PE) into ethylene and propylene will enable closed-loop recycling of plastics. Conventional catalytic cracking of PE is restricted by kinetic entanglement between the formation of main products and by-products, limiting ethylene and propylene yields to less than 25%. Here we address this challenge with a kinetic decoupling–recoupling (KDRC) strategy, achieving yields of ethylene and propylene up to 79% from PE conversion using a tandem reactor with dual zeolite catalysts. Reaction kinetics analysis, synchrotron-based vacuum ultraviolet photoionization mass spectrometry and in situ neutron powder diffraction reveal that KDRC decouples kinetics of PE cracking to intermediates (butenes and pentenes) in the first stage and synchronizes this process with dimerization–β-scission reactions in the second stage. This synchronization minimizes by-products and enhances ethylene and propylene production substantially. Combined with high catalytic stability, this KDRC strategy represents a robust pathway to combating plastic pollution via a circular economy.
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