Compared to Two Kinds of Methods for the Degradation of an Anthraquinone Dye Reactive Brilliant Blue KN-R

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Taking anthraquinone dye reactive brilliant blue KN-R as a target pollutant, this paper studied KN-R degradation rates and electric generation performances in the system of Fe2+/PDS and Fe2+/PDS-MFC. The Fe2+/PDS system is that persulfate (PDS) is activated by ferrous iron (Fe2+) ,while Fe2+/PDS-MFC system is using Fe2+/PDS system as the cathode of microbial fuel cells (MFC) .The results showed that in the two systems, the KN-R degradation rate was increased and then decreased with the increase of initial Fe2+ dosage. With the increase of pH, the KN-R degradation rapid declines. In the two systems, both of the KN-R degradation reaction was divided into two stages. In addition, the process of reaction conforms to the first-order kinetic equation. Compared with Fe2+/PDS system, the Fe2+/PDS-MFC system’s ability to degrade pollutants have little change, the main advantage of Fe2+/PDS-MFC system is able to obtain higher and more stable power. Under an optimal condition, the maximum power density achieved 294.07 mW/m2, the KN-R degradation rate was 96.90%.

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Advanced Materials Research (Volumes 955-959)

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2254-2260

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June 2014

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] J. M. Fanchiang, D. H. Tseng. Chemosphere Vol. 77(2) (2009), 214-221.

Google Scholar

[2] T. Robinson, G. McMullan, R. Marchant, P. Nigam. Bioresource technology Vol. 77(3) (2001), 247-255.

Google Scholar

[3] X. R. Xu, X. Z. Li. Separation and Purification Technology Vol. 72(1) (2010), 105-111.

Google Scholar

[4] A. Rastogi, S. R. Al-Abed, D. D. Dionysiou. Water Research Vol. 43(3) (2009), 684-694.

Google Scholar

[5] S. Yang, P. Wang, X. Yang, L. Shan, W. Y. Zhang, X. T. Shao, R. Niu. Journal of Hazardous Materials Vol. 179(1) (2010), 552-558.

Google Scholar

[6] C. Choi, Y. Cui. Bioresource Technology Vol. 107(2012), 522-525.

Google Scholar

[7] R. D. Cusick, P. D. Kiely, B. E. Logan. International Journal of Hydrogen Energy Vol. 35(17)(2010), 8855-8861.

Google Scholar

[8] Y. Wang, C. G. Niu, G. M. Zeng, W. J. Hu, D. W. Huang. International Journal of Hydrogen Energy Vol. 36(23) (2011), 15344-15351.

Google Scholar

[9] D. R. Lovely, E. J. P Phillips. Appl. Environ. Microbiol. Vol. 54(1988), 1472–1480.

Google Scholar

[10] X. Jiang, Y. Wu, P. Wang, H. Li, W. Dong. Environmental Science and Pollution Research Vol. 20(7)( 2013), 4947-4953.

Google Scholar

[11] J. Deng, Y. Shao, N. Gao, Y. Deng, C. Tan, S. Zhou. International Journal of Environmental Science and Technology (2013) http: /link. springer. com/article/10. 1007/s13762-013-0284-2.

Google Scholar

[12] W. J. Mcelroy, S. J. Waygood. Journal of the Chemical Society, Faraday Transactions Vol, 86 (14)(1990), 2557–2564.

Google Scholar

[13] J. Li, Q. Fu, Q. Liao, X. Zhu, D. Ye, X. Tian. Journal of Power Sources Vol. 194(1)(2009), 268-274.

Google Scholar

[14] C.G. Niu, Y. Wang, X. G. Zhang, G. M. Zeng, D. W. Huang. Bioresource technology Vol. 126(2012), 101-106.

Google Scholar