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多相催化剂上甘油的催化转移氢解:机理研究综述

Catalytic Transfer Hydrogenolysis of Glycerol over Heterogeneous Catalysts: A Short Review on Mechanistic Studies.

作者信息

Liu Xi, Yin Bin, Zhang Wenxiang, Yu Xiao, Du Yiyao, Zhao Siming, Zhang Guangyu, Liu Mengyuan, Yan Hao, Abbotsi-Dogbey Manuela, Al-Absi Saleem T, Yeredil Sayan, Yang Chaohe, Shen Jian, Yan Wenjuan, Jin Xin

机构信息

State Key Laboratory of Heavy Oil Processing, College of Chemical Engineering, China University of Petroleum, No. 66 Changjiang West Road, Qingdao, Shandong Province, 266580, China.

College of Fisheries, Southwest University, No.2 Tiansheng Road, Beibei District, Chongqing, 400715, China.

出版信息

Chem Rec. 2021 Jul;21(7):1792-1810. doi: 10.1002/tcr.202100037. Epub 2021 May 11.

Abstract

Catalytic transfer hydrogenolysis, using liquid H-donors in the absence of pressurized H under mild temperatures, is regarded as the most important technology to substitute traditional hydrogenation processes in industry. Despite decade development with several breakthroughs in catalyst design, the reaction mechanism involved in H generation and subsequent hydrogenolysis reactions is still under debate. In this review, transfer hydrogenolysis of glycerol, as a representative example, on metallic catalysts is revised critically with respect to surface reaction mechanism and catalyst design. The detailed reaction pathways for propanol, methanol, formic acid and ethanol for H generation have been discussed systematically. In particular, reaction mechanism for catalytic C-H cleavage, H spillover/transfer and C-O cleavage reaction steps will be critically revised with experimental and theoretical results in literature. Insights into reaction pathways, mechanism and H transfer efficiency and structure-performance relation for Pd, Cu and Ni catalysts will be provided for future development of catalyst manufacture and process development. The outcome of this work is useful for successful implementation of bio-refinery.

摘要

在温和温度下,使用液体氢供体且无需加压氢气的催化转移氢解反应,被视为工业中替代传统氢化工艺的最重要技术。尽管经过了十年的发展,在催化剂设计方面取得了多项突破,但氢生成及后续氢解反应所涉及的反应机理仍存在争议。在本综述中,以甘油的转移氢解反应为例,对金属催化剂上的表面反应机理和催化剂设计进行了批判性修订。系统地讨论了丙醇、甲醇、甲酸和乙醇生成氢的详细反应途径。特别是,将结合文献中的实验和理论结果,对催化碳氢键断裂、氢溢流/转移和碳氧键断裂反应步骤的反应机理进行批判性修订。将为钯、铜和镍催化剂的反应途径、机理、氢转移效率以及结构-性能关系提供见解,以促进催化剂制造和工艺开发的未来发展。这项工作的成果有助于生物炼制的成功实施。

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