Polyethylene upcycling to long-chain alkylaromatics by tandem hydrogenolysis/aromatization

Author:

Zhang Fan1ORCID,Zeng Manhao2ORCID,Yappert Ryan D.3ORCID,Sun Jiakai2ORCID,Lee Yu-Hsuan2ORCID,LaPointe Anne M.4ORCID,Peters Baron3ORCID,Abu-Omar Mahdi M.12ORCID,Scott Susannah L.12ORCID

Affiliation:

1. Department of Chemical Engineering, University of California, Santa Barbara, CA 93106, USA.

2. Department of Chemistry and Biochemistry, University of California, Santa Barbara, CA 93106, USA.

3. Department of Chemical Engineering, University of Illinois, Urbana-Champaign, IL 61801, USA.

4. Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14583, USA.

Abstract

A new future for polyethylene Most current plastic recycling involves chopping up the waste and repurposing it in materials with less stringent engineering requirements than the original application. Chemical decomposition at the molecular level could, in principle, lead to higher-value products. However, the carbon-carbon bonds in polyethylene, the most common plastic, tend to resist such approaches without exposure to high-pressure hydrogen. F. Zhang et al. now report that a platinum/alumina catalyst can transform waste polyethylene directly into long-chain alkylbenzenes, a feedstock for detergent manufacture, with no need for external hydrogen (see the Perspective by Weckhuysen). Science , this issue p. 437 ; see also p. 400

Funder

U.S. Department of Energy

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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