4.6 Article

Direct conversion of CO2 into methanol over promoted indium oxide-based catalysts

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APPLIED CATALYSIS A-GENERAL
卷 583, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.apcata.2019.117144

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Methanol synthesis; CO2 hydrogenation; Indium oxide; Yttrium; Lanthanum

资金

  1. U.S. Army [GTS-S-17-013]

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Supported indium oxide catalysts are investigated for the CO2 hydrogenation to methanol at a total pressure of 40 bar (528-573 K) using a laboratory flow reactor. Surface reducibility, optical spectral characteristics, and catalytic rates and selectivity were correlated to catalyst composition. Promoted catalysts, especially Yttrium or Lanthanum-promoted indium oxide, require higher temperatures (H-2-TPR) for surface reduction and display higher CO2 desorption temperatures (CO2-TPD). The promoted samples also have (similar to)20% higher methanol selectivity compared to the non-promoted catalyst, while having similar methanol formation rates (0.330-0.420 g(MeOH) g(cat).(-1) h(-1) at 573 K). From 528 K to 558 K, methanol selectivity was over 80%, over all the promoted catalysts, and nearly 100% selectivity was observed at the low temperature range ((similar to)528 K) investigated. The reaction kinetics of Y-promoted catalyst and the results of CO co-feeding experiments suggest that formate pathway is the likely reaction mechanism for methanol formation.

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