Longbo Zhang, Jia Guo, Yanyan Wang, Ying Wang, Jie Li, Hongxing Wang, Chenglong Yu, Yanru Zhang, Jun He, Xianyu Meng, Zhuo Zhang, Tianbin Wu, Qingli Qian, Li Tan, Buxing Han
{"title":"Synthesis of ethanol via methanol homologation with CO2 and H2 using an industrially relevant Ru–Co catalyst","authors":"Longbo Zhang, Jia Guo, Yanyan Wang, Ying Wang, Jie Li, Hongxing Wang, Chenglong Yu, Yanru Zhang, Jun He, Xianyu Meng, Zhuo Zhang, Tianbin Wu, Qingli Qian, Li Tan, Buxing Han","doi":"10.1039/d6cy00285d","DOIUrl":null,"url":null,"abstract":"<div><div>Homogeneously catalyzed ethanol synthesis from CO<sub>2</sub> and H<sub>2</sub> usually uses expensive, unstable and complex catalyst precursors, hindering their industrial viability. In this work, a homogeneous catalytic system consisting of economic and stable catalyst precursors (RuCl<sub>3</sub>·3H<sub>2</sub>O and CoCl<sub>2</sub>·6H<sub>2</sub>O), cocatalyst (LiI) and <em>N</em>-ethyl-2-pyrrolidone (NEP) solvent was designed to accelerate ethanol production <em>via</em> methanol homologation with CO<sub>2</sub> and H<sub>2</sub>. After activation of the catalyst precursors at 200 °C with CO, the target reaction could proceed efficiently under mild conditions (170 °C), with top level reaction selectivity (64.9%) and much higher space time yield (STY) of ethanol (3.9 g L<sup>−1</sup> h<sup>−1</sup>) compared to previous reports with Ru/Co catalysts. The impact of activation conditions, reaction conditions, and the catalytic mechanism of the reaction were studied by a series of control experiments. This method of ethanol production has the advantages of a stable and easily available catalyst, excellent performance, and easy separation and recycling of the catalyst, showing great potential for industrialization.</div></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"16 12","pages":"Pages 4068-4077"},"PeriodicalIF":4.0000,"publicationDate":"2026-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475326002376","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/18 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Homogeneously catalyzed ethanol synthesis from CO2 and H2 usually uses expensive, unstable and complex catalyst precursors, hindering their industrial viability. In this work, a homogeneous catalytic system consisting of economic and stable catalyst precursors (RuCl3·3H2O and CoCl2·6H2O), cocatalyst (LiI) and N-ethyl-2-pyrrolidone (NEP) solvent was designed to accelerate ethanol production via methanol homologation with CO2 and H2. After activation of the catalyst precursors at 200 °C with CO, the target reaction could proceed efficiently under mild conditions (170 °C), with top level reaction selectivity (64.9%) and much higher space time yield (STY) of ethanol (3.9 g L−1 h−1) compared to previous reports with Ru/Co catalysts. The impact of activation conditions, reaction conditions, and the catalytic mechanism of the reaction were studied by a series of control experiments. This method of ethanol production has the advantages of a stable and easily available catalyst, excellent performance, and easy separation and recycling of the catalyst, showing great potential for industrialization.
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A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
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