Cellulose hydrothermal conversion promoted by heterogeneous Bronsted and Lewis acids: Remarkable efficiency of solid Lewis acids to produce lactic acid

被引:228
作者
Chambon, Flora [1 ]
Rataboul, Franck [1 ]
Pinel, Catherine [1 ]
Cabiac, Amandine [2 ]
Guillon, Emmanuelle [2 ]
Essayem, Nadine [1 ]
机构
[1] CNRS, IRCELYON, F-69626 Villeurbanne, France
[2] IFP Energies Nouvelles, F-69360 Solaize, France
关键词
Cellulose hydrolysis; Solid Lewis acid catalysts; Tungstated zirconia; Tungstated alumina; Lactic acid; CATALYTIC CONVERSION; HYDROLYSIS; GLUCOSE; WATER; CSXH3-XPW12O40; DYNAMICS;
D O I
10.1016/j.apcatb.2011.04.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Crystalline cellulose treated in hydrothermal conditions (190 degrees C, 24h) is partially solubilised, 30%, into water soluble oligosaccharides/polymers with the formation of small amounts of glucose and 5-HMF. In the presence of solid Bronsted catalysts such as Cs2HPW12O40 and HY zeolite, the extent of the cellulose depolymerisation was not changed when no leaching occurred. However, a quite different products distribution was obtained, in favour of further transformations of glucose and HMF in levulinic and formic acids. On the opposite, solid Lewis acids such as tungstated zirconia (ZrW) and tungstated alumina (AIW) exhibited a remarkable promoting effect on the cellulose depolymerisation which was raised up to 45% while an unexpected decrease of the proportion of water soluble oligosaccharides/polymers was observed. Yields of 27 mol% and 18.5 mol% in lactic acid were achieved on AIW and ZrW, respectively. Moreover, these tungsten based Lewis acids exhibited a good stability and recyclability. The efficiency of the solid Lewis acids ZrW and AIW to produce lactic acid directly from crystalline cellulose was explained by a positive synergy between water autoprotolysis responsible of the cellulose depolymerisation into soluble intermediates which are further converted on the solid Lewis catalyst surface. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 181
页数:11
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