Recent advances in the methanol carbonylation reaction into acetic acid

被引:135
作者
Kalck, Philippe [1 ]
Le Berre, Carole [1 ]
Serp, Philippe [1 ]
机构
[1] Univ Toulouse, UPS INP, Composante ENSIACET Inst Natl Polytech Toulouse, CNRS,UPR 8241,Lab Chim Coordinat, 4 Allee Emile Monso, F-31030 Toulouse 4, France
关键词
VAPOR-PHASE CARBONYLATION; NICKEL-ACTIVE-CARBON; RHODIUM-CATALYZED CARBONYLATION; DIMETHYL ETHER CARBONYLATION; TRANSITION-METAL CATALYSTS; MIGRATORY CO INSERTION; OXIDATIVE ADDITION; METHYL ACETATE; ORGANIC-COMPOUNDS; DIPHOSPHINE LIGANDS;
D O I
10.1016/j.ccr.2019.213078
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Although the high efficiency of the homogeneous processes, using rhodium or iridium complexes, was clearly demonstrated industrially, heterogeneous catalysts offer the advantages of facile product separation and vapor phase operation, which often limit catalyst losses. Both noble and non-noble metal homogeneous and heterogeneous catalyzed carbonylation of methanol have been studied for many years. In this short chapter, we intend to analyze the recent evolutions of the most promising catalytic systems for this important reaction of catalysis. A presentation by metals was chosen, always referring to the origins of the first catalytic systems. (C) 2019 Elsevier B.V. All rights reserved.
引用
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页数:14
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