Catalytic deconstruction of waste polyethylene with ethylene to form propylene

Author:

Conk Richard J.12ORCID,Hanna Steven12ORCID,Shi Jake X.12ORCID,Yang Ji2ORCID,Ciccia Nicodemo R.12ORCID,Qi Liang23,Bloomer Brandon J.12ORCID,Heuvel Steffen1ORCID,Wills Tyler1,Su Ji2ORCID,Bell Alexis T.23ORCID,Hartwig John F.12ORCID

Affiliation:

1. Department of Chemistry, University of California, Berkeley, Berkeley, CA 94720, USA.

2. Division of Chemical Sciences, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

3. Department of Chemical and Biomolecular Engineering, University of California, Berkeley, Berkeley, CA 94720, USA.

Abstract

The conversion of polyolefins to monomers would create a valuable carbon feedstock from the largest fraction of waste plastic. However, breakdown of the main chains in these polymers requires the cleavage of carbon–carbon bonds that tend to resist selective chemical transformations. Here, we report the production of propylene by partial dehydrogenation of polyethylene and tandem isomerizing ethenolysis of the desaturated chain. Dehydrogenation of high-density polyethylene with either an iridium-pincer complex or platinum/zinc supported on silica as catalysts yielded dehydrogenated material containing up to 3.2% internal olefins; the combination of a second-generation Hoveyda-Grubbs metathesis catalyst and [PdP( t Bu) 3 (μ-Br)] 2 as an isomerization catalyst selectively degraded this unsaturated polymer to propylene in yields exceeding 80%. These results show promise for the application of mild catalysis to deconstruct otherwise stable polyolefins.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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