Electrochemical Degradation of Benzene in Water Using Platinum Supported on Carbon Black Materials

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Abstract:

This study investigated the feasibility of the electrochemical degradation of benzene (C6H6) in a NaCl electrolyte solution between 0.05 and 0.5 M under the temperature of 298 K and reaction concentration between 1.28×10-5 and 1.28×10-3 M with an applied potential of 3 V was conducted in this study to investigate the destruction of the C6H6 in the batch reactors using a Pt/XC-72 composite as a catalyst. Experimental results indicated that the optimal conditions in the reaction were developed as a NaCl solution with 0.1 M at pH of 1.0 under C6H6 concentration of 6.41×10-4 M. The results reveal that electrochemical degradation of C6H6 in acidic medium is highly effective, while a maximum about 41% reduction at 120 min was achieved with Pt/XC-72 composite during the electrochemical degradation. In comparsion, the removal efficiency reached only 29% with the Pt electrode, showing the suitability of the Pt/XC-72 composites for electro-oxidation of C6H6. As a result, XC-72 carbon black materials played an important role in the decomposition of C6H6. Furthermore, the Pt/XC-72 composite used in this research has been developed as a potential catalyst for the application of C6H6 electro-oxidation.

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Advanced Materials Research (Volumes 1044-1045)

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43-46

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October 2014

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] S.H. Liang, C.M. Kao, Y.C. Kuo, K.F. Chen, B.M. Yang, Water Res. 45 (2011) 2496–2506.

Google Scholar

[2] M. Ioth, W.C. Xu, S. Hara, K. Sakaki, Catal. Today 56 (2000) 307–314.

Google Scholar

[3] J. Sanabria-Chinchilla, J.H. Baricuatro, M.P. Soriaga, F. Hernandez, H. Baltruschat, J. Colloid Interface Sci. 314 (2007) 152–159.

DOI: 10.1016/j.jcis.2007.05.024

Google Scholar

[4] J.C. Farmer, F.T. Wang, R.A. Hawley-Fedder, P.R. Lewis, L.J. Summers, L. Foiles, J. Electrochem. Soc. 139 (1992) 654–662.

DOI: 10.1149/1.2069280

Google Scholar

[5] I. Cesarino, V. Cesarino, F.C. Moraes, T.C.R. Ferreira, M.R.V. Lanza, L.H. Mascaro, S.A.S., Mat. Chem. Phys. 141 (2013) 304–309.

DOI: 10.1016/j.matchemphys.2013.05.015

Google Scholar

[6] X. Yu, S. Ye, J. Power Sources 172 (2007) 145–154.

Google Scholar

[7] F.J. Vidal-Iglesias, J. Solla-Gullón, J.M. Feliu, H. Baltruschat, A. Aldaz, J. Electroanal. Chem. 588 (2006) 331–338.

DOI: 10.1016/j.jelechem.2006.01.009

Google Scholar