The Key Laboratory of Orogenic Belts and Crustal Evolution, School of Earth and Space Sciences, Peking University, Beijing 100871, PR China.
Bioresour Technol. 2010 May;101(10):3500-5. doi: 10.1016/j.biortech.2009.11.107. Epub 2010 Jan 25.
Reductive decolorization of azo dye in wastewater was investigated in a dual-chamber microbial fuel cell (MFC) equipped with cathodes made of graphite or rutile-coated graphite. Rapid reduction of methyl orange (MO) with concomitant electricity production was achieved when the rutile-coated cathode was irradiated by visible light. The electrochemical impedance spectra (EIS) indicate that the polarization resistance (R(p)) of the rutile-cathode MFC decreased from 1378 Omega in dark to 443.4 Omega in light, demonstrating that photocatalysis of rutile can enhance the cathodic electron transfer process. The combination of the biologically active anode and photocatalysis-supported cathodic reduction of MO obeyed the pseudo-first-order kinetics. The analysis of decolorization products indicates that the azo bond of MO was probably cleaved by photoelectrons at the irradiated rutile-cathode, resulting in the products of colorless hydrazine derivatives. In addition, concurrently enhanced electricity generation in the MFCs involving photocatalyzed cathodic reduction of MO was observed throughout this study.
在配备有石墨或锐钛矿涂覆石墨制成的阴极的双室微生物燃料电池(MFC)中研究了废水中偶氮染料的还原脱色。当锐钛矿涂覆的阴极受到可见光照射时,甲基橙(MO)迅速还原并同时产生电能。电化学阻抗谱(EIS)表明,锐钛矿阴极 MFC 的极化电阻(R(p))从黑暗中的 1378 Ω降低到光中的 443.4 Ω,表明锐钛矿的光催化作用可以增强阴极电子转移过程。具有生物活性的阳极和 MO 的光催化支持的阴极还原的组合遵循准一级动力学。脱色产物的分析表明,MO 的偶氮键可能是由照射在锐钛矿阴极上的光电子断裂的,导致无色腙衍生物的产物。此外,在这项研究中还观察到涉及 MO 的光催化阴极还原的 MFC 中同时增强的发电。