Related Experiment Video
Updated: May 16, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Conversion of polyethylene to monoaromatics via a tandem catalytic strategy
Zhiye Ma1, Ziyu Cen1, Tianrui Bi1
1Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China; School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 101408, China.
Abstract:
The catalytic conversion of polyethylene (PE) waste into high-value aromatics, particularly benzene-toluene-xylene (BTX), remains a challenge in chemical recycling. We present a tandem two-stage fixed-bed system that efficiently converts PE into BTX without requiring noble-metal catalysts or external hydrogen acceptors. The process achieves an aromatics yield of 59.9%, including a BTX yield of 51.5%, which represents 86% of the total aromatics produced. In the first stage, PE undergoes near-complete catalytic cracking over a layered self-pillared zeolite (LSP-Z100). The second stage employs a dual-catalyst configuration where Ga/LSP-Z100 promotes aromatization of cracking intermediates, while Co/LSP-Z100 adsorbs small alkanes, catalyzes their dehydrogenation to olefins, and cleaves low-value polycyclic aromatic hydrocarbons to enhance BTX production. The catalyst maintains stable performance over five consecutive cycles and yields approximately 55% aromatics from real plastic waste. This tandem catalytic strategy offers a highly effective and sustainable route for the valorization of PE waste into high-value aromatic chemicals.
More Related Videos
Related Concept Videos
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Free-Radical Chain Reaction and Polymerization of Alkenes
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction

