Impact of oleic acid on the fermentation of glucose and xylose mixtures to hydrogen and other byproducts

被引:9
作者
Chaganti, Subba Rao [1 ]
Kim, Dong-Hoon [2 ]
Lalman, Jerald A. [1 ]
机构
[1] Univ Windsor, Dept Civil & Environm Engn, Windsor, ON N9B 3P4, Canada
[2] Korea Inst Energy Res, Wastes Energy Res Ctr, Taejon 305343, South Korea
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrogen; Mixed anaerobic cultures; Lignocellulosic materials; Glucose; Xylose; Oleic acid; CHAIN FATTY-ACIDS; PH;
D O I
10.1016/j.renene.2011.09.015
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
Using low value lignocellulosic feedstocks to produce hydrogen (H-2) could be a more economically viable option in comparison to grains derived from agriculture crops. The glucose and xylose composition of lignocellulosic feedstocks is relatively high and can vary from 55-65% to 35-45%, respectively. Mixed anaerobic cultures which are suitable for fermentative H-2 production are capable of utilizing a variety of substrates. However, the H-2 yields from mixed anaerobic cultures are low because of the syntrophic association between H-2 producers and H-2 consumers. In this study, oleic acid (OA) was used to control the growth of H-2 consumers and hence, increase the H-2 yield. The H-2 yield was affected by changing the glucose to xylose ratio. In control cultures, the H-2 yield (1.6 +/- 0.32 mol H-2 mol(-1) glucose) was low because the electron flux was diverted towards the formation of propionate and methane in addition to acetate and butyrate. In presence of 2000 mg L-1 OA, 60-70% of the electron fluxes were diverted towards acetate and butyrate production and this resulted in a maximum H-2 yield of 2.84 +/- 0.24 mol H-2 mol(-1) glucose. This study revealed that the addition of OA to the mixed anaerobic cultures is an effective method for diverting the electron fluxes to H-2 instead of CH4. Based on a principal component analysis 1 (PCA 1), the control cultures were related; however, in case of the OA treated cultures, they were related in terms of PCA 1 and PCA 2. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:60 / 65
页数:6
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