Carbon dioxide reduction by mixed and pure cultures in microbial electrosynthesis using an assembly of graphite felt and stainless steel as a cathode

被引:230
作者
Bajracharya, Suman [1 ,2 ]
ter Heijne, Annemiek [2 ]
Benetton, Xochitl Dominguez [1 ]
Vanbroekhoven, Karolien [1 ]
Buisman, Cees J. N. [2 ]
Strik, David P. B. T. B. [2 ]
Pant, Deepak [1 ]
机构
[1] Flemish Inst Technol Res VITO, Separat & Convers Technol, Mol, Belgium
[2] Wageningen Univ, Subdept Environm Technol, NL-6700 AP Wageningen, Netherlands
关键词
Microbial electrosynthesis; CO2; reduction; Biocathode; Hydrogen evolution; Bioproduction; BIOELECTROCHEMICAL SYSTEMS; GEOBACTER-SULFURREDUCENS; METABOLIC INTERACTIONS; ACETOGENIC BACTERIA; ANAEROBIC-DIGESTION; ELECTRON-TRANSFER; ACETATE; CO2; METHANE; GAS;
D O I
10.1016/j.biortech.2015.05.081
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Carbon dioxide (CO2) reduction to multi-carbon compounds at the cathode using chemolithoautotrophs is an emerging application of microbial electrosynthesis (MES). In this study, CO2 reduction in MES was investigated at hydrogen evolving potentials, separately by a mixed culture and Clostridium ljungdahlii, using a graphite felt and stainless steel assembly as cathode. The mixed culture reactor produced acetate at the maximum rate of 1.3 mM d(-1), along with methane and hydrogen at -1.1 V/(Ag/AgCl). Over 160 days of run-time in four fed-batches, 26% of bicarbonate was converted to acetate between day 28 and 41, whereas in the late batches, methane production prevailed. Out of 45 days of run-time in the C. ljungdahlii reactor, 2.4 mM d(-1) acetate production was achieved at -0.9 V/(Ag/AgCl) in Batch 1. Simultaneous product degradation occurred when the mixed culture was not selectively enriched. Hydrogen evolution is potentially the rapid way of transferring electrons to the biocatalysts for higher bioproduction rates. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:14 / 24
页数:11
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