4.8 Review

Recent advances in the routes and catalysts for ethanol synthesis from syngas

Journal

CHEMICAL SOCIETY REVIEWS
Volume 51, Issue 13, Pages 5606-5659

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cs01003k

Keywords

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Funding

  1. National Key R&D Program of China [2018YFB1501403]
  2. Strategic Priority Research Program of Chinese Academy of Sciences [XDA 21060800]
  3. New Energy and Industrial Technology Development Organization of Japan
  4. Japan Science and Technology Agency [MIRAI-JPMJMI17E2]
  5. Award Program for the Fujian Minjiang Scholar Professorship [0040/511076]

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Ethanol, as an important bulk chemical, is widely used in modern society. Conversion of syngas to ethanol (STE) is the most environmentally friendly and economical process. This review summarizes and analyzes the routes and catalyst designs used in STE technology. The goal is to provide a comprehensive perspective on STE technology and inspire the invention of new catalysts and pathway designs in the future.
Ethanol, as one of the important bulk chemicals, is widely used in modern society. It can be produced by fermentation of sugar, petroleum refining, or conversion of syngas (CO/H-2). Among these approaches, conversion of syngas to ethanol (STE) is the most environmentally friendly and economical process. Although considerable progress has been made in STE conversion, control of CO activation and C-C growth remains a great challenge. This review highlights recent advances in the routes and catalysts employed in STE technology. The catalyst designs and pathway designs are summarized and analysed for the direct and indirect STE routes, respectively. In the direct STE routes (i.e., one-step synthesis of ethanol from syngas), modified catalysts of methanol synthesis, modified catalysts of Fischer-Tropsch synthesis, Mo-based catalysts, noble metal catalysts and multifunctional catalysts are systematically reviewed based on their catalyst designs. Further, in the indirect STE routes (i.e., multistep processes for ethanol synthesis from syngas via methanol/dimethyl ether as intermediates), carbonylation of methanol/dimethyl ether followed by hydrogenation, and coupling of methanol with CO to form dimethyl oxalate followed by hydrogenation, are outlined according to their pathway designs. The goal of this review is to provide a comprehensive perspective on STE technology and inspire the invention of new catalysts and pathway designs in the near future.

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