Multi response optimization of waste activated sludge oxidation and azo dye reduction in microbial fuel cell

被引:8
作者
Piskin, Elif Durna [1 ]
Genc, Nevim [1 ,2 ]
机构
[1] Kocaeli Univ, Fac Engn, Dept Environm Engn, Kocaeli, Turkiye
[2] Kocaeli Univ, Fac Engn, Dept Environm Engn, TR-41000 Kocaeli, Turkiye
关键词
Activated sludge oxidation; azo dye removal; bioelectricity; microbial fuel cells; optimization; ELECTRICITY-GENERATION; SURFACE METHODOLOGY; WATER; DEGRADATION; WASTEWATERS; RECOVERY; IMPACT;
D O I
10.1080/09593330.2023.2179422
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Microbial fuel cell technology draws attention with its ability to directly recover electrical energy from various organic materials. In this study, the operating conditions affecting the oxidation-reduction and electricity generation efficiency of MFC were optimized using the Taguchi Experimental Design model. Optimization was carried out for maximum power density, coulombic efficiency, azo dye removal, and COD removal. With the determined optimum conditions (cathode pH of 3.0, cathode oxygen status of anaerobic, anode substrate of pre-treated, external resistance of 100 omega, cathode electrode type of plain carbon, cathode electrode surface of 22 cm(2), cathode conductivity of 20 mu s/cm), 177.03 mW/m(2) power density, 7.50% coulombic efficiency, 91.26% azo dye removal efficiency and 21.61% COD removal efficiency were obtained. By Pareto analysis, it was determined that the power density, coulombic efficiency and COD removal efficiency were most affected by the substrate type at the anode, and the azo dye removal was most affected by the catholyte pH. The maximum power density and internal resistance of the MFC operated under optimum conditions were determined as 145.11 mW/m(2) and 243.30 omega, respectively by the polarization curve. Cyclic voltammetry was also performed for the electrochemical characterization of MFC operated under optimum conditions. An anodic peak at -183.2 mV and a cathodic peak at -181.2 mV was visible in the CV curve.
引用
收藏
页码:2599 / 2611
页数:13
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