Coking Reduction of Cr‐loaded Beta Zeolite during Polymer Cracking: Hydrocracking of Aromatics by Synergistic Effect of Cr6+ and Zeolitic Acid Sites

Author:

Kokuryo Shinya1,Tamura Kazuya1,Tsubota Soshi1,Miyake Koji12ORCID,Uchida Yoshiaki1,Mizusawa Atsushi3,Kubo Tadashi3,Nishiyama Norikazu12

Affiliation:

1. Division of Chemical Engineering Graduate School of Engineering Science Osaka University Nanoreaction Engineering Group (Nishiyama Lab.) Toyonaka, Osaka 560-8531 Japan

2. Innovative Catalysis Science Division Institute for Open and Transdisciplinary Research Initiatives (ICS-OTRI) Osaka University Suita Osaka 565-0871 Japan

3. AC Biode Co., Ltd. Sakyo Kyoto 606-0024 Japan

Abstract

AbstractZeolite deactivation induced by coke deposition is a critical problem in the industrialization of the chemical recycling (CR) of plastics. We previously demonstrated that Cr6+ species bonded to silanol groups in the zeolite framework inhibit coke deposition in low‐density polyethylene (LDPE) cracking. In this study, the role of Cr6+ species and the mechanism of coke reduction were determined experimentally. During LDPE cracking, hydrogen was generated from the alkane products at the Cr6+ sites. Furthermore, the hydrogenation and decomposition of aromatics, which are coke precursors, occurred at the zeolitic acid sites, resulting in the reduction of coke deposition. Owing to the synergistic effect of the Cr6+ and zeolitic acid sites, coke reduction was achieved without reducing cracking activity.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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