Selective electrocatalytic semihydrogenation of acetylene impurities for the production of polymer-grade ethylene

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Jun Bu - , Northwestern Polytechnical University Xian (Author)
  • Zhenpeng Liu - , Northwestern Polytechnical University Xian (Author)
  • Wenxiu Ma - , Northwestern Polytechnical University Xian (Author)
  • Lei Zhang - , Northwestern Polytechnical University Xian (Author)
  • Tao Wang - , Westlake University (Author)
  • Hepeng Zhang - , Northwestern Polytechnical University Xian (Author)
  • Qiuyu Zhang - , Northwestern Polytechnical University Xian (Author)
  • Xinliang Feng - , Chair of Molecular Functional Materials (cfaed) (Author)
  • Jian Zhang - , Northwestern Polytechnical University Xian (Author)

Abstract

The current thermocatalytic acetylene hydrogenation process suffers from the use of excessive hydrogen and the noble metal Pd, high temperatures and overhydrogenation. Here we report an electrocatalytic semihydrogenation strategy to selectively reduce acetylene impurities to ethylene under ambient conditions. For a crude ethylene flow that contains 1 × 104 ppm acetylene, electrochemically deposited Cu dendrites exhibited a high specific selectivity of 97%, continuous production of a polymer-grade ethylene stream (4 ppm acetylene) at a large space velocity of 9.6 × 104 ml gcat–1 h–1 and excellent long-term stability. Theoretical and operando electrochemical Raman investigations revealed that the outstanding electrocatalytic acetylene semihydrogenation performance of Cu catalysts originates from its exothermic acetylene adsorption and ethylene desorption. Meanwhile, the electrocatalytic semihydrogenation strategy is universally applicable for hydrogenating other alkyne impurities to produce polymer-grade olefins, for example, propylene and 1,3-butadiene. [Figure not available: see fulltext.]

Details

Original languageEnglish
Pages (from-to)557-564
Number of pages8
JournalNature Catalysis
Volume4
Issue number7
Publication statusPublished - Jul 2021
Peer-reviewedYes