Abstract
A double chambered microbial fuel cell (MFC) showed enormous capacity in the simultaneous degradation of synthetic wastewater and dihydroxybenzene isomers (catechol, resorcinol and hydroquinone) and concurrently with bioelectricity generation. Operating parameter such as effect of catalyst on MFC system was evaluated using bare carbon plate and copper (II) oxide (CuO) loaded carbon plate as cathodes, respectively, in terms of chemical oxygen demand (COD) and dihydroxybenzene isomers removal efficiency, maximum voltage output and power density. Results revealed that the application of CuO loaded carbon plate was more effective in the COD removal of synthetic wastewater in the anodic chamber and degradation of dihydroxybenzene isomers in the cathodic chamber. Compared with the bare carbon plate as cathode, the COD removal efficiency of synthetic wastewater, removal rate of dihydroxybenzene isomers and maximum voltage output increased 20, 100 and 31 %, respectively, when CuO was applied as cathodic catalyst. Among the dihydroxybenzene isomers, hydroquinone exhibited the best performance in both absence and presence of catalyst in the MFC. The position of the substituent of hydroxyl groups possessed significant effect on the reaction rate, reactivity and conductivity of dihydroxybenzene isomers. Hydroquinone was more susceptible to be degraded than that of catechol and resorcinol due to its lower dipole moment which eased the bond cleavage. The intermediate products of degradation of catechol, resorcinol and hydroquinone were determined using gas chromatograph-mass spectrometer and the degradation pathways were proposed.
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