Enhanced reductive degradation of methyl orange in a microbial fuel cell through cathode modification with redox mediators

2010 ◽  
Vol 89 (1) ◽  
pp. 201-208 ◽  
Author(s):  
Rong-Hua Liu ◽  
Guo-Ping Sheng ◽  
Min Sun ◽  
Guo-Long Zang ◽  
Wen-Wei Li ◽  
...  
2013 ◽  
Vol 291-294 ◽  
pp. 602-605 ◽  
Author(s):  
Liang Liu ◽  
Wen Yi Zhang

In this study we investigated the use of a microbial fuel cell (MFC) to abioticlly cathodic decolorization of a model azo dye, Methyl Orange (MO). Experimental results showed that electricity could be continuously generated the MO-fed MFC and MO was successfully decolorized in the cathode. The decolorization rate was highly dependent on the catholyte pH. When pH was varied from 3.0 to 9.0, the k value in relation to MO degradation decreased from 0.298 to 0.016 μmol min-1, and the maximum power density decreased from 34.77 to 1.51 mW m-2. Sulfanilic acid and N,N-dimethyl-p-phenylenediamine were identified as the decolorization products of MO by HPLC-MS.


2008 ◽  
Vol 74 (14) ◽  
pp. 4472-4476 ◽  
Author(s):  
Moustafa Malki ◽  
Antonio L. De Lacey ◽  
Nuria Rodríguez ◽  
Ricardo Amils ◽  
Victor M. Fernandez

ABSTRACT Several anaerobic metal-reducing bacteria have been shown to be able to donate electrons directly to an electrode. This property is of great interest for microbial fuel cell development. To date, microbial fuel cell design requires avoiding O2 diffusion from the cathodic compartment to the sensitive anodic compartment. Here, we show that Acidiphilium sp. strain 3.2 Sup 5 cells that were isolated from an extreme acidic environment are able to colonize graphite felt electrodes. These bacterial electrodes were able to produce high-density electrocatalytic currents, up to 3 A/m2 at a poised potential of +0.15 V (compared to the value for the reference standard calomel electrode) in the absence of redox mediators, by oxidizing glucose even at saturating air concentrations and very low pHs.


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