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Kinetics of Degradation of Bisphenol A by Ozonization in Aqueous Solution
Corresponding Author(s) : Shouhua Jia
Asian Journal of Chemistry,
Vol. 27 No. 7 (2015): Vol 27 Issue 7, 2015
Abstract
The degradation of bisphenol A in aqueous solution by ozonization was investigated at the laboratory scale. The primary factors that influenced the removal efficiency of bisphenol A were investigated, including the pH, the initial concentration of bisphenol A, the ozone gas concentration and the reaction temperature. Ozone enabled the efficient removal of bisphenol A and the maximum removal efficiency was achieved at pH 7. An accurate kinetic model of the chemical reaction and mass transfer was described by an exponential relationship between the pseudo-first-order rate constant and the operational parameters. The intrinsic kinetic constants for the reaction of bisphenol A with ozone were also determined using a competitive kinetics method with phenol as a reference compound. The results revealed that the pH exerted a strong influence on the kinetic constants and that the rate constants increased exponentially from 3.27 × 103 M-1 s-1 to 1.23 × 109 M-1 s-1 as the pH was increased from 3 to 11, respectively.
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M. Sugiura-Ogasawara, Y. Ozaki, S.-i. Sonta, T. Makino and K. Suzumori, Hum. Reprod., 20, 2325 (2005); doi:10.1093/humrep/deh888.
N. Olea, R. Pulgar, P. Pérez, F. Olea-Serrano, A. Rivas, A. Novillo-Fertrell, V. Pedraza, A.M. Soto and C. Sonnenschein, Environ. Health Perspect., 104, 298 (1996); doi:10.1289/ehp.96104298.
C. Gupta, Proc. Soc. Exp. Biol. Med., 224, 61 (2000); doi:10.1046/j.1525-1373.2000.22402.x.
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T. Garoma and S. Matsumoto, J. Hazard. Mater., 167, 1185 (2009); doi:10.1016/j.jhazmat.2009.01.133.
C.A. Staples, P.B. Dome, G.M. Klecka, S.T. Oblock and L.R. Harris, Chemosphere, 36, 2149 (1998); doi:10.1016/S0045-6535(97)10133-3.
M.F.L. Lemos, C.A.M. Gestel and A.M.V.M. Soares, J. Soils Sediments, 9, 492 (2009); doi:10.1007/s11368-009-0104-y.
L.N. Vandenberg, R. Hauser, M. Marcus, N. Olea and W.V. Welshons, Reprod. Toxicol., 24, 139 (2007); doi:10.1016/j.reprotox.2007.07.010.
S. Jayashree, D. Indumathi, N. Akilavalli, S. Sathish, J. Selvaraj and K. Balasubramanian, Environ. Toxicol. Pharmacol., 35, 300 (2013); doi:10.1016/j.etap.2012.12.016.
Z. Qiang, H. Dong, B. Zhu, J. Qu and Y. Nie, Chemosphere, 92, 986 (2013); doi:10.1016/j.chemosphere.2013.03.019.
B. Gözmen, M.A. Oturan, N. Oturan and O. Erbatur, Environ. Sci. Technol., 37, 3716 (2003); doi:10.1021/es034011e.
Z. Frontistis, V.M. Daskalaki, A. Katsaounis, I. Poulios and D. Mantzavinos, Water Res., 45, 2996 (2011); doi:10.1016/j.watres.2011.03.030.
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D. Bing-zhi, W. Lin and G. Nai-yun, Desalination, 221, 312 (2008); doi:10.1016/j.desal.2007.01.088.
G. Xiao, L. Fu and A. Li, Chem. Eng. J., 191, 171 (2012); doi:10.1016/j.cej.2012.02.092.
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T. Garoma, S. Matsumoto, Y. Wu and R. Klinger, Ozone Sci. Eng., 32, 338 (2010); doi:10.1080/01919512.2010.508484.
M. Deborde, S. Rabouan, J.-P. Duguet and B. Legube, Environ. Sci. Technol., 39, 6086 (2005); doi:10.1021/es0501619.
J. Lee, H. Park and J. Yoon, Environ. Technol., 24, 241 (2003); doi:10.1080/09593330309385555.
A. Alvares, C. Diaper and S. Parsons, Environ. Technol., 22, 409 (2001); doi:10.1080/09593332208618273.
K.S. Tay, N.A. Rahman and M.R.B. Abas, Maejo Int. J. Sci. Technol., 6, 77 (2012).
I. Arslan-Alaton and A.E. Caglayan, Chemosphere, 59, 31 (2005); doi:10.1016/j.chemosphere.2004.10.014.
R. Keykavoos, R. Mankidy, H. Ma, P. Jones and J. Soltan, Sep. Purif. Technol., 107, 310 (2013); doi:10.1016/j.seppur.2013.01.050.
F. Wang, Y. Wang and M. Ji, J. Hazard. Mater., 123, 145 (2005); doi:10.1016/j.jhazmat.2005.03.033.
C.-H. Ko, C.-Y. Guan, P.-J. Lu and J.-M. Chern, Chem. Eng. J., 171, 1045 (2011); doi:10.1016/j.cej.2011.04.059.
J. Hoigné and H. Bader, Water Res., 17, 173 (1983); doi:10.1016/0043-1354(83)90098-2.
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J. Staehelin and J. Hoigne, Environ. Sci. Technol., 19, 1206 (1985); doi:10.1021/es00142a012.