Investigation of deactivation mechanisms of a solid acid catalyst during esterification of the bio-oils from mallee biomass

被引:47
|
作者
Hu, Xun [1 ]
Lievens, Caroline [1 ]
Mourant, Daniel [1 ]
Wang, Yi [1 ]
Wu, Liping [1 ]
Gunawan, Richard [1 ]
Song, Yao [1 ]
Li, Chun-Zhu [1 ]
机构
[1] Curtin Univ Technol, Fuels & Energy Technol Inst, Perth, WA 6845, Australia
关键词
Bio-oil esterification; Metal ions; Ion exchange; Polymer; Catalyst deactivation and regeneration; FAST PYROLYSIS; TRANSPORTATION FUELS; REACTION PATHWAYS; ACETIC-ACID; CONVERSION; METHANOL; CRACKING;
D O I
10.1016/j.apenergy.2013.04.078
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
This study reports the deactivation mechanisms of the solid acid catalyst Amberlyst 70 during the esterification of bio-oils from mallee biomass and the methods for catalyst regeneration. The metal ions in bio-oil deactivated Amberlyst 70 via ion exchange with the hydrogen ions on/in catalyst, which changed structure of catalysts and reduced availability of acidic sites. N-containing organics reacted with the hydrogen ions on/in catalyst, forming neutral salts and resulting in complete catalyst deactivation. Polymers formed during the esterification of bio-oils deposited on/in catalyst, reducing the accessibility of catalytic sites. Washing with solvents could remove some adsorbed organics and restore some catalytic activity but not much. In comparison, ion exchange in a concentrated sulfuric acid removes most of metal ions and the N-containing organics and significantly improves the catalytic activity. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:94 / 103
页数:10
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