Porous nanomaterials as green catalyst for the conversion of biomass to bioenergy

被引:101
作者
Bhanja, Piyali [1 ]
Bhaumik, Asim [1 ]
机构
[1] Indian Assoc Cultivat Sci, Dept Mat Sci, Kolkata 700032, India
关键词
Biomass conversion; Porous nanomaterials; HMF; Heterogeneous catalysis; SOLID ACID CATALYSTS; METAL-ORGANIC FRAMEWORK; CARBON BEARING SO3H; IONIC-LIQUID; AEROBIC OXIDATION; LIGNOCELLULOSIC BIOMASS; SELECTIVE CONVERSION; MESOPOROUS-CARBON; LEVULINIC ACID; 2,5-FURANDICARBOXYLIC ACID;
D O I
10.1016/j.fuel.2016.08.004
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Natural fossil fuel is the prime resource of energy and with the rapid technological development its reserve is depleting at an alarming rate. To overcome this concern bio-refinery is the most emerging and necessary approach, where liquid fuels and related demanding fine chemicals can be derived very effectively from biomass via platform chemical 5-hydroxymethylfurfural (HMF). HMF, furfural and 2,5-furandicarboxylic acid (FDCA) can be derived from biomass via several catalytic processes. Thus the objective of this review is to summarize various catalytic methods to produce 5-hydroxymethylfurfural (HMF) the precursor of 2,5-dimethylfuran (DMF) from a variety of monomeric bioresources such as glucose, fructose, dimeric (sucrose) and also polymeric carbohydrates like starch, cellulose and biomass derived carbohydrates (raw biomass). High surface acidity and porous nanostructures (high surface area) of the nanomaterials play crucial role in these heterogeneous catalytic processes. Several nanoporous solid acid catalysts like porous resin, micro/mesoporous carbons, microporous zeolites, mesoporous metal oxides, functionalized mesoporous silicas and porous organic polymers employed in the selective biomass conversion reactions are discussed in detail in this review. Bifunctional catalysts, MOFs and metal phosphonates with functionalised surfaces in comparison to those of the conventional solid acid catalysts are also discussed in-depth. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:432 / 441
页数:10
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