Boosting Selective Oxidation of Ethylene to Ethylene Glycol Assisted by In situ Generated H O from O Electroreduction.

Angew Chem Int Ed Engl

State Key Laboratory of Fine Chemicals, Liaoning Key Laboratory for Catalytic Conversion of Carbon Resources, School of Chemical Engineering, Dalian University of Technology, Dalian, 116024, Liaoning, China.

Published: May 2023


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Article Abstract

Ethylene glycol is a useful organic compound and chemical intermediate for manufacturing various commodity chemicals of industrial importance. Nevertheless, the production of ethylene glycol in a green and safe manner is still a long-standing challenge. Here, we established an integrated, efficient pathway for oxidizing ethylene into ethylene glycol. Mesoporous carbon catalyst produces H O , and titanium silicalite-1 catalyst would subsequently oxidize ethylene into ethylene glycol with the in situ generated H O . This tandem route presents a remarkable activity, i.e., 86 % H O conversion with 99 % ethylene glycol selectivity and 51.48 mmol g  h production rate at 0.4 V vs. reversible hydrogen electrode. Apart from generated H O as an oxidant, there exists ⋅OOH intermediate which could omit the step of absorbing and dissociating H O over titanium silicalite-1, showing faster reaction kinetics compared to the ex situ one. This work not only provides a new idea for yielding ethylene glycol but also demonstrates the superior of in situ generated H O in tandem route.

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http://dx.doi.org/10.1002/anie.202302466DOI Listing

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