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

  • Ziyu Cen,
  • Xue Han,
  • Longfei Lin,
  • Sihai Yang,
  • Wanying Han,
  • Weilong Wen,
  • Wenli Yuan,
  • Minghua Dong,
  • Zhiye Ma,
  • Fang Li,
  • Yubin Ke,
  • Juncai Dong,
  • Jin Zhang,
  • Shuhu Liu,
  • Jialiang Li,
  • Qian Li,
  • Ningning Wu,
  • Junfeng Xiang,
  • Hao Wu,
  • Lile Cai,
  • Yanbo Hou,
  • Yongqiang Cheng,
  • Luke L. Daemen,
  • Anibal J. Ramirez-Cuesta,
  • Pilar Ferrer,
  • David C. Grinter,
  • Georg Held,
  • Yueming Liu,
  • Buxing Han

摘要

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.