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

IF 4.9 RSC sustainability Pub Date : 2024-11-21 DOI:10.1039/D4SU00484A
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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H-MFI型沸石催化剂对聚丙烯形状选择性裂化的影响及环辛烷溶剂的回收
沸石催化聚烯烃裂解采用烃类溶剂,使产物分子量分布变窄,提高了聚烯烃化学再循环制取石脑油的效率,而石脑油是聚烯烃的关键前驱体。然而,溶剂消耗仍然是一个挑战。在本研究中,利用沸石微孔来实现聚烯烃的形状选择性裂解,同时允许溶剂回收。以H-MFI型沸石催化剂和环辛烷为溶剂,对聚丙烯进行了选择性转化,无环辛烷反应性。在典型情况下,84%的聚丙烯转化为C3-27脂肪族和单环芳香族化合物(相当于液化石油气、石脑油、煤油、喷气和柴油),选择性为79%,而环辛烷的回收率为95%。这项研究首次证明了在酸性沸石上裂解聚烯烃时溶剂的可回收性,有助于聚烯烃化学再循环成其前驱体石脑油,溶剂的存在促进了高选择性,但不消耗溶剂。
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