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

被引:88
作者
Chou, Chen-Yu [1 ]
Lobo, Raul F. [1 ]
机构
[1] Univ Delaware, Ctr Catalyt Sci & Technol, Dept Chem & Biomol Engn, Newark, DE 19716 USA
关键词
Methanol synthesis; CO2; hydrogenation; Indium oxide; Yttrium; Lanthanum; COPPER-BASED CATALYSTS; CARBON-DIOXIDE HYDROGENATION; HYDROTALCITE-LIKE PRECURSORS; ACTIVE-SITE; PERFORMANCE; PRESSURE; ZIRCONIA; SELECTIVITY; ADSORPTION; MECHANISM;
D O I
10.1016/j.apcata.2019.117144
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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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页数:9
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