Enhancing anaerobic digestibility of lignin-rich submerged macrophyte using thermochemical pre-treatment

被引:34
作者
Koyama, Mitsuhiko [1 ]
Yamamoto, Shuichi [1 ]
Ishikawa, Kanako [2 ]
Ban, Syuhei [3 ]
Toda, Tatsuki [1 ]
机构
[1] Soka Univ, Grad Sch Engn, Hachioji, Tokyo 1928577, Japan
[2] Lake Biwa Environm Res Inst, Otsu, Shiga 5200022, Japan
[3] Univ Shiga Prefecture, Sch Environm Sci, Hikone, Shiga 5228533, Japan
关键词
Anaerobic processes; Waste treatment; Biodegradation; Biogas; Lignin; Pre-treatment; Inhibition; METHANE PRODUCTION; STRUCTURAL FEATURES; BIOGAS PRODUCTION; SOUTHERN BASIN; WATER HYACINTH; LAKE BIWA; BIOMASS; DIGESTION; BIODEGRADABILITY; HYDROLYSIS;
D O I
10.1016/j.bej.2015.03.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The present study investigated the effect of alkaline thermochemical pre-treatment on anaerobic digestibility of two submerged macrophyte species which have significantly different lignin content. The highest hydrolysis efficiency was achieved at NaOH loading rate of 0.20 gg-TSsubstrate-1, 80 degrees C, 3.0 h for both species. Alkaline delignification was much conspicuous in lignin-rich macrophyte (Potamogeton maackianus) as compared with lignin-poor macrophyte (Egeria densa). Ferulic acid, which is cross-linked with lignin polymer and polysaccharides, remarkably declined with increase of NaOH loading rate. It suggests that alkali removed lignin-ferulate complex from the surface of polysaccharides. The CH4 yield of pre-treated P. maackianus was 243 mLg-VS-1, which is 51% higher than the un-treated (161 mLg-VS-1). In contrast, the CH4 yield of pre-treated E. densa was 24% higher than the un-treated. These results indicated that alkaline thermochemical pre-treatment could be an effective method for anaerobic digestion of lignin-rich macrophytes. However, it was also suggested that the high NaOH addition to lignin-rich macrophyte possibly inhibit the methane recovery, due to the increase of solubilized lignin in the digestate. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:124 / 130
页数:7
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