Shape selective cracking of polypropylene on an H-MFI type zeolite catalyst with recovery of cyclooctane solvent†

Tomohiro Fukumasa, Yuya Kawatani, Hiroki Masuda, Ikuto Nakashita, Ryusei Hashiguchi, Masanori Takemoto, Satoshi Suganuma, Etsushi Tsuji, Toru Wakaihara and Naonobu Katada
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Abstract

The use of hydrocarbon solvents for zeolite-catalyzed polyolefin cracking narrows the molecular weight distribution of the products, which enhances the efficiency of polyolefin chemical recycling to naphtha, a key precursor to polyolefins. However, solvent consumption remains a challenge. In this study, zeolite microporosity was used to achieve shape-selective polyolefin cracking while allowing solvent recovery. With an H-MFI type zeolite catalyst combined with cyclooctane as the solvent, polypropylene was selectively converted without cyclooctane reactivity. In a typical case, 84% of polypropylene was converted into C3-27 aliphatic and monocyclic aromatic compounds (equivalent to liquid petroleum gas, naphtha, kerosene, jet and diesel) with 79% selectivity, while 95% of cyclooctane was recovered. This study is the first to demonstrate solvent recyclability in polyolefin cracking on an acidic zeolite, contributing to the chemical recycling of polyolefin into its precursor, naphtha, with high selectivity facilitated by the presence of solvent but without solvent consumption.

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Inside back cover Back cover Afterglow quenching in plasma-based dry reforming of methane: a detailed analysis of the post-plasma chemistry via kinetic modelling. Showcasing the technological advancements of carbon dioxide conversion: a pathway to a sustainable future From lead–acid batteries to perovskite solar cells – efficient recycling of Pb-containing materials†
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