Upcycling of polyethylene to gasoline through a self-supplied hydrogen strategy in a layered self-pillared zeolite

Z. H. Cen(Chinese Academy of Sciences), Xue Han(Beijing Normal University), Longfei Lin(Chinese Academy of Sciences), Sihai Yang⧫(Peking University), Wanying Han(East China Normal University), Weilong Wen(Chinese Academy of Sciences), Wen‐Li Yuan(Chinese Academy of Sciences), Minghua Dong(Chinese Academy of Sciences), Zhiye Ma(Chinese Academy of Sciences), Fang Li(East China Normal University), Yubin Ke(China Spallation Neutron Source), Juncai Dong(Chinese Academy of Sciences), Jin Zhang(Chinese Academy of Sciences), Shuhu Liu(Chinese Academy of Sciences), Jialiang Li(Chinese Academy of Sciences), Qian Li(Chinese Academy of Sciences), Ningning Wu(Chinese Academy of Sciences), Junfeng Xiang(Chinese Academy of Sciences), Hao Wu(Sinopec (China)), Lile Cai(Sinopec (China)), Yanbo Hou(Sinopec (China)), Yongqiang Cheng(Oak Ridge National Laboratory), Luke L. Daemen(Oak Ridge National Laboratory), Anibal J. Ramirez‐Cuesta(Oak Ridge National Laboratory), Pilar Ferrer(Diamond Light Source), David C. Grinter(Diamond Light Source), Georg Held(Diamond Light Source), Yueming Liu(East China Normal University), Buxing Han(Beijing National Laboratory for Molecular Sciences)
Nature Chemistry
April 9, 2024
Cited by 135Open Access
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Abstract

Conversion of plastic wastes to valuable carbon resources without using noble metal catalysts or external hydrogen remains a challenging task. Here we report a layered self-pillared zeolite that enables the conversion of polyethylene to gasoline with a remarkable selectivity of 99% and yields of >80% in 4 h at 240 °C. The liquid product is primarily composed of branched alkanes (selectivity of 72%), affording a high research octane number of 88.0 that is comparable to commercial gasoline (86.6). In situ inelastic neutron scattering, small-angle neutron scattering, solid-state nuclear magnetic resonance, X-ray absorption spectroscopy and isotope-labelling experiments reveal that the activation of polyethylene is promoted by the open framework tri-coordinated Al sites of the zeolite, followed by β-scission and isomerization on Brönsted acids sites, accompanied by hydride transfer over open framework tri-coordinated Al sites through a self-supplied hydrogen pathway to yield selectivity to branched alkanes. This study shows the potential of layered zeolite materials in enabling the upcycling of plastic wastes.


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