| Literature DB >> 35681045 |
Francesca Arcudi1,2, Luka Ðorđević1,2,3, Neil Schweitzer4, Samuel I Stupp1,2,3,5,6,7, Emily A Weiss8,9,10.
Abstract
The production of polymers from ethylene requires the ethylene feed to be sufficiently purified of acetylene contaminant. Accomplishing this task by thermally hydrogenating acetylene requires a high temperature, an external feed of H2 gas and noble-metal catalysts. It is not only expensive and energy-intensive, but also prone to overhydrogenating to ethane. Here we report a photocatalytic system that reduces acetylene to ethylene with ≥99% selectivity under both non-competitive (no ethylene co-feed) and competitive (ethylene co-feed) conditions, and near 100% conversion under the latter industrially relevant conditions. Our system uses a molecular catalyst based on earth-abundant cobalt operating under ambient conditions and sensitized by either [Ru(bpy)3]2+ or an inexpensive organic semiconductor (metal-free mesoporous graphitic carbon nitride) under visible light. These features and the use of water as a proton source offer advantages over current hydrogenation technologies with respect to selectivity and sustainability.Entities:
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Year: 2022 PMID: 35681045 DOI: 10.1038/s41557-022-00966-5
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.274