Degradation of crystal violet using copper modified iron oxide as heterogeneous photo-fenton reagent
Subject Areas : Journal of the Iranian Chemical ResearchPinki B. Punjabi 1 , Noopur Ameta 2 , Jyoti Sharma 3 , Kiran Chanderia Rakshit Ameta 4
1 - Photochemistry Laboratory, Department of Chemistry, University College of Science, M. L.
Sukhadia University, Udaipur, India
2 - Photochemistry Laboratory, Department of Chemistry, University College of Science, M. L.
Sukhadia University, Udaipur, India
3 - Photochemistry Laboratory, Department of Chemistry, University College of Science, M. L.
Sukhadia University, Udaipur, India
4 - Photochemistry Laboratory, Department of Chemistry, University College of Science, M. L.
Sukhadia University, Udaipur, India
Keywords: Heterogeneous photo–Fenton reagent, Copper modified iron oxide, Crystal violet,
Abstract :
The heterogeneous photo-Fenton degradation of crystal violet under visible light has been investigated usingcopper modified iron oxide. The photocatalyst has been prepared by coprecipitation method. The rate ofphotocatalyic degradation of dye was monitored spectrophotometrically. It has been observed thatphotocatalytic degradation follows pseudo first order kinetics. The effect of various parameters like pH,concentration of dye, amount of photocatalyst, amount of H2O2 and light intensity on the rate of photo-Fenton degradation has also been observed. Photocatalyst has been characterized by IR spectroscopy,scanning electron microscopy and X-ray diffraction. Chemical Oxygen Demand (COD) of the reactionmixture before and after exposure was determined. A tentative mechanism for the photocatalytic degradationof crystal violet has also been proposed. Involvement of •OH radicals has been confirmed by usingisopropanol and butylated hydroxy toluene (BHT) as •OH radical scavengers. It has been observed that rateof reaction is drastically reduced in the presence of these scavangers. Under similar conditions Fe2O3 hasalso been prepared. The efficiency of Fe2O3 and copper modified Fe2O3 has been compared for thephotocatalytic degradation of crystal violet.NN+NCl-Structure of crystal violet
[1] A. G. Vlyssides, D. Papaioannou, M. Loizido, P. K. Karlis, A. A. Zorpas, Waste Manage. 20 (2000) 569-
574.
[2] Y.-C. Li, L. -D. Zou, E. Hu, J. Environ. Sci. 16 (2004) 375-379.
[3] A. F. Martins, M. L. Wilde, C. Dasilveira, J. Environ. Sci. Health. 41 (2006) 675-685.
[4] H. J. H. Fenton, J. Chem. Soc. 65 (1894) 899-911.
[5] A. G. Vlyssides, H. Loukakis, P. K. Karlis, Environ. Technol. 24 (2003) 931-935.
[6] S. Lee, J. Oh, Y. Park, Bull. Korean Chem. Soc. 27 (2006) 489-494.
[7] L. Gomathi Devi, K. S. Anantha Raju, S. Girish Kumar, J. Environ. Monit. 11 (2009) 1397-1404.
[8] T. M. El-Morsi, M. M. Emara, M. H. Hassan, Abd El Bary, A. S. Abd-El-Aziz, K. J. Friesen,
Chemosphere 47 (2002) 343–348.
[9] P. B. Punjabi, R. Ameta, D. Vaya, S Lodha, J. Serb. Chem. Soc. 73 (2008) 631-639.
[10] P. B. Punjabi, V. K. Sharma, A. Jain, S. Lodha, Ind. J. Chem. 47A (2008) 397-400.
[11] F. Duarte, L. M. Madeira, Separ. Sci. Technol. 45 (2010) 1512-1520.
[12] N. Soon, B. H. Hameed, Desalination 269 (2011) 1-16.
[13] F. Martínez, G. Calleja, J. A. Melero, R. Molina, Appl. Catal. B: Environ. 60 (2005) 181–190.
[14] H. Li, P. Wu, Z. Dang, N. Zhu, P. Li J. Wu, Clays Clay Miner. 59 (2011) 435-437.
[15] J. Y. Feng, X. J. Hu., P. L. Yue, H. Y. Zhu, G. Q. Lu, Wat. Res. 37 (2003) 3776-3784.
[16] L. Liu., G. Zhang, L. Wang, T. Huang, L. Qin, Ind. Eng. Chem. Res. 50 (2011) 7219–7227.
[17] Q. Chen, P. Wu, Y. Li, N. Zhu, Z. Dang, J. Hazard. Mater. 168 (2009) 901-908.
[18] B. De la Plata, O. M. Alfano, A. E. Cassano, Appl. Catal. B. 95 (2010) 14-25.
[19] S. Yang, H. He, D. Wu, D. Chen, Y. Ma, X. Li, J. Zhu, P. Yuan, Ind. Eng. Chem. Res. 48 (2009)
9915–9921.
[20] A. Jain, S. Lodha, P.B. Punjabi, V.K. Sharma, S.C. Ameta, Ind. Acad. Sci., 121 (2009) 1027-1034.
[21] J. Sharma, R. Ameta, V. K. Sharma, P. B. Punjabi, Bull. Catal. Soc. Ind. 9 (2010) 99-106.
[22] G. Velraj, K. Prabhakaran, A. Mohamad Musthafa, R. Hemamalini, Ind. Rec. Res. Sci. Technol. 2