催化作用
聚乙烯
路易斯酸
异构化
产量(工程)
布朗斯特德-洛瑞酸碱理论
有机化学
辛烷值
汽油
选择性
材料科学
化学
高分子化学
复合材料
作者
Wanying Han,Longfei Lin,Z. H. Cen,Yubin Ke,Qian Xu,Junfa Zhu,Xuelei Mei,Zhanghui Xia,Xinrui Zheng,Yaqin Wang,Yani Liu,Mingyuan He,Haihong Wu,Buxing Han
标识
DOI:10.1002/anie.202417923
摘要
Abstract Branched alkanes, which enhance the octane number of gasoline, can be produced from waste polyethylene. However, achieving highly selective production of branched alkanes presents a significant challenge in the upcycling of waste polyethylene. Here, we report a one‐pot process to convert polyethylene into gasoline‐range hydrocarbons (C 4 –C 13 ) with yield of 73.3 % over SO 4 /ZrO 2 ‐Al 2 O 3 catalyst at 280 °C. The proportion of branched alkanes reaches 90.1 % within the C 4 –C 13 fraction. Incorporation of sulfate group endows the catalyst with strong Lewis acid sites and weak and moderate Brønsted acid sites. In situ X‐ray absorption, in situ infrared spectroscopy, in situ small angle neutron scattering, and DFT calculations reveal that polyethylene activation occurs through the synergy between sulfate groups and strong Lewis acid sites (Zr sites). The weak and moderate Brønsted acid sites preferentially catalyze the isomerization and type A β‐scission processes, which favors the formation of branched alkanes, while suppressing competing reactions that produce straight‐chain alkanes.
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