4.5 Article

Yttria-doped Cu/ZnO catalyst with excellent performance for CO2 hydrogenation to methanol

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MOLECULAR CATALYSIS
卷 509, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.mcat.2021.111641

关键词

CO2 hydrogenation to methanol; Cu/ZnO catalyst; the promotion of yttria

资金

  1. National Key Research and Development Program of China [2017YFB0603301]
  2. Doctoral Fund of Ministry of Education of China [2017M621315]
  3. Fundamental Research Funds for the Central Universities [DUT17GJ204]
  4. Xinjiang Dunhua Petroleum Technology Co., Ltd.

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The research findings suggest that the addition of yttria (Y2O3) can enhance the performance of the Cu/ZnO catalyst for CO2 hydrogenation to methanol. The newly synthesized Cu/ZnO/Y2O3 catalyst showed higher methanol yield and selectivity due to small, well-dispersed Cu species, abundant surface adsorption sites, and more Cu-ZnO interfaces. This basic design strategy offers a promising approach for developing scalable and cost-effective catalysts for industrial methanol synthesis.
Revealing the origin of the enhanced performance on yttria (Y2O3) promoted Cu/ZnO based catalyst for methanol synthesis via CO2 hydrogenation is still challenging. To shed light upon the promotion effect of Y2O3 modifier on binary Cu/ZnO catalyst for CO2 hydrogenation reaction, a ternary Cu/ZnO/Y2O3 catalyst was synthesized via a citric acid coordination-assisted strategy. The developed Cu/ZnO/Y2O3 catalyst exhibited a remarkably higher Weight-time yeild of methanol (236.8 gMeOH g(cat)(-1).h(-1)) and methanol selectivity (81.1%) in comparison to Cu/ZnO catalyst (159.6 g(MeOH) g(cat)(-1).h(-1) and 73.9%, respectively). Various characterizations results have uncovered the enhanced catalytic activity of Cu/ZnO/Y2O3 catalyst for methanol synthesis was associated with small size and highly dispersed Cu species and abundant surface adsorption sites as well as more Cu-ZnO interfaces with strong interaction. Moreover, the Cu/ZnO/Y2O3 catalyst displayed a superior weight-time yield of methanol with a time-on-stream of 100 h in comparison with classic Cu/ZnO catalyst. We anticipate that this basic design strategy will provide a novel alternative to expand opportunities to explore scalable, cost-effective catalysts for industrial methanol synthesis.

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