石脑油
微型多孔材料
双功能
介孔材料
催化作用
材料科学
化学工程
聚乙烯
石油化工
选择性
铂金
多孔性
沸石
聚合物
双功能催化剂
纳米技术
化学
二乙胺
聚烯烃
有机化学
作者
Guojing Shi,Zhenlei Zhang,Yuliang Li,Xiaochun Zhu,Zhenchen Tang,Zhentao Chen,Y Chen,Jiaqi Feng,bingyu li,Xi Zhang
标识
DOI:10.1021/acssuschemeng.5c13791
摘要
The chemical upcycling of polyethylene (PE) into high-value naphtha is hindered by the inherent diffusion limitations of microporous zeolites and the destructive nature of conventional mesopore engineering. Herein, we utilize a transformative inner pore-directing agent (iPDA) strategy to fabricate hierarchical Beta zeolites that decouple mesopore formation from the loss of catalytic activity. By preadsorbing diethylamine (DEA) to shield intrinsic micropores during alkaline etching, we created a robust, interconnected mesoporous network (pore diameters >25 nm) while preserving critical Brønsted acid sites. When paired with an ultralow platinum loading (0.1 wt % Pt), this bifunctional catalyst achieves near-complete PE conversion (>99%) with an exceptional naphtha (C5–C12) selectivity exceeding 90% at 280 °C. This performance significantly outperforms conventional alkali-treated zeolites, which suffer from acidity depletion. Our findings demonstrate that strategic iPDA modification provides a scalable and efficient pathway for the precision design of catalysts capable of deconstructing macromolecular plastic waste into circular chemical feedstocks.
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