Synthesis of nanostructured carbon on graphite electrodes with a supported Co catalyst for preparing anodes for microbial fuel cells

被引:0
作者
Kovalenko, G. A. [1 ,2 ]
Chuenko, T. V. [1 ]
Perminova, L. V. [1 ]
Rudina, N. A. [1 ]
Sherstyuk, O. V. [1 ,2 ]
Tyurin-Kuzmin, A. Yu. [3 ]
Smirnov, I. A. [3 ]
机构
[1] Russian Acad Sci, Siberian Branch, Boreskov Inst Catalysis, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Novosibirsk 630090, Russia
[3] Russian Acad Sci, Inst Biomed Problems, Moscow 123007, Russia
关键词
Co catalyst; nanostructured carbon; C-3 and C-4 alkane pyrolysis; microbial fuel cell; anode; SHEWANELLA-ONEIDENSIS MR-1; MUTANTS;
D O I
10.1134/S0023158416010079
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis of nanostructured carbon (NSC) on graphite electrodes with a supported Co catalyst by C-3 and C-4 alkane pyrolysis in the presence of hydrogen has been investigated. Co(II) hydroxo compounds have been deposited onto graphite, and a Co/graphite catalyst has been prepared by the homogeneous precipitation of divalent cobalt from cobalt nitrate solutions in the presence of urea and compounds containing OH groups, namely, lower alcohols (ethanol, n-propanol, and n-butanol) and polyols (ethylene glycol, glycerol, and sorbitol). The effect of Co catalyst preparation conditions on the pyrolytic activity of the catalyst and on the morphology of the synthesized NSC has been investigated. An active Co/graphite catalyst forms in the presence of an alcohol containing 1-3 OH groups. A fairly uniform NSC layer on the graphite surface is obtained at Co(II) nitrate concentrations of 0.05-0.1 mol/L, a urea concentration of 1 mol/L, and glycerol concentrations of 5-20 vol %. The electrochemical characteristics of the electrodes prepared and those of a microbial fuel cell (MFC) involving an NSC/graphite anode and an activated-sludge microbial consortium have been determined. The maximum power of the MFC under the conditions examined is 4.8 mW per square meter of the anode's geometric surface area.
引用
收藏
页码:104 / 112
页数:9
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