Heterogeneous catalysis for bio-based polyester monomers from cellulosic biomass: advances, challenges and prospects

被引:139
作者
De Clercq, R. [1 ]
Dusselier, M. [1 ]
Sels, B. F. [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Celestijnenlaan 200F, B-3001 Heverlee, Belgium
关键词
ONE-POT CONVERSION; LACTIC-ACID PRODUCTION; LIQUID-PHASE DEHYDRATION; SELECTIVE AEROBIC OXIDATION; MEERWEIN-PONNDORF-VERLEY; RING-OPENING POLYMERIZATION; ETHYLENE-GLYCOL PRODUCTION; SOLID LEWIS-ACIDS; 2,5-FURANDICARBOXYLIC ACID; METHYL LACTATE;
D O I
10.1039/c7gc02040f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is a 21st century challenge to develop a more sustainable chemical industry where fossil-based resources are, where possible, preferentially replaced by renewable alternatives. Bio-based polymers, in particular those derived from cellulose or other carbohydrates, are often considered benign alternatives for petrochemical plastics. The majority of bioplastic precursors are currently derived from fermentation or biotechnology. Chemocatalytic routes to both similar and new polymer building blocks are emerging in an effort to mitigate challenges related to carbohydrate fermentation, such as waste generation and costly product purification. This review critically surveys recent developments in applying heterogeneous catalysis for the production of bio-based polyester monomers from cellulose or cellulose-derived carbohydrates. Highlighted target molecules include various alpha-hydroxy acids or esters (e.g. lactic and glycolic acid, lactide and methyl vinyl glycolate), furandicarboxylic acid, ethylene glycol and isosorbide. The production of lactic acid from glycerol will exceptionally be included as well, as an oversupply of glycerol might contribute to non-negligible amounts of lactic acid in the future. Where possible, remaining challenges and future prospects are highlighted.
引用
收藏
页码:5012 / 5040
页数:29
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