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Science ; 377(6614): 1561-1566, 2022 09 30.
Artigo em Inglês | MEDLINE | ID: mdl-36173865

RESUMO

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(tBu)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.


Assuntos
Alcenos , Etilenos , Polietileno , Gerenciamento de Resíduos , Alcenos/síntese química , Carbono/química , Catálise , Etilenos/química , Irídio , Platina , Polienos , Polietileno/química , Dióxido de Silício , Gerenciamento de Resíduos/métodos
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