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

Nature Chemistry 2024 111 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 65 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Z. H. Cen, Xue Han, Jin Zhang, Longfei Lin, Sihai Yang⧫, Wanying Han, Wanying Han, Weilong Wen, Weilong Wen, Wen‐Li Yuan, Wen‐Li Yuan, Minghua Dong, Minghua Dong, Zhiye Ma, Zhiye Ma, Buxing Han Fang Li, Yubin Ke, Juncai Dong, Jin Zhang, Shuhu Liu, Jialiang Li, Qian Li, Ningning Wu, Ningning Wu, Junfeng Xiang, Hao Wu, Lile Cai, Lile Cai, Yanbo Hou, Yanbo Hou, Yongqiang Cheng, Luke L. Daemen, Luke L. Daemen, Anibal J. Ramirez‐Cuesta, Pilar Ferrer, David C. Grinter, Georg Held, Yueming Liu, Buxing Han

Summary

Researchers developed a special zeolite material (a porous mineral catalyst) that converts polyethylene plastic waste into high-quality gasoline with over 80% yield, without needing expensive metals or added hydrogen. This breakthrough offers a practical pathway for recycling one of the most common plastics into usable fuel, potentially reducing plastic waste and reliance on fossil fuel extraction.

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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