The experimental investigation of bisphenol A degradation by Fenton process with different types of cyclodextrins

Wenjing Chen; Changjun Zou; Yuan Liu; Xiaoke Li

Journal of Industrial and Engineering Chemistry, Vol.56, 428-434, December, 2017

DOI10.1016/j.jiec.2017.07.042 Export Citation

The experimental investigation of bisphenol A degradation by Fenton process with different types of cyclodextrins

Wenjing Chen, Changjun Zou^†, Yuan Liu, and Xiaoke Li¹

College of Chemistry and Chemical Engineering, Southwest Petroleum University, PR China
¹Organic Chemicals Co., Ltd., Chinese Academy of Sciences, Chengdu 610041, PR China

E-mail:

In this work, the degradation efficiencies of bisphenol A (BPA) by Fenton reaction were compared systematically with varying cyclodextrins. The results showed that the removal rate of BPA displays a considerable increase by Fenton reaction in presence of β-cyclodextrin (β-CD) and its derivatives. Specifically, 98 ± 2% and 89 ± 2% of BPA was removed with carboxymethyl-β-cyclodextrin (CMCD) and β-CD, respectively. Additionally, to understand the reaction mechanism, the structure activity of cyclodextrins with substrate and the kinetic of Fenton reaction with cyclodextrins have been investigated. Results showed that the structure activity was the major role for cyclodextrins in this system.

Keywords:Remediation;Bisphenol A;Advanced oxidation processes (AOPs);Cyclodextrins

[References]

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Lindsey ME, Tarr MA, Chemosphere, 41, 409 (2000)
Canals M, Gonzalez-Olmos R, Costas M, Company A, Environ. Sci. Technol., 47, 9918 (2013)
ElShafei GMS, Yehia FZ, Dimitry OIH, Badawi AM, Eshaq G, Appl. Catal. B: Environ., 99(1-2), 242 (2010)
Sillanpaa MET, Res. J. Chem. Environ., 13, 99 (2009)
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[Referenced By]

[1] Rebuli ME, Cao JY, Sluzas E, Delclos KB, Camacho L, Lewis SM, Vanlandingham MM, Patisaul HB, Toxicol. Sci., 140, 190 (2014)

[2] Lee MS, Lee YS, Lee HH, Song HY, J. Occup. Med. Toxicol., 7 (2012)

[3] Hussain I, Bhan A, Ansari KI, Deb P, Bobzean SAM, Perrotti LI, Mandal SS, BBA Gene Regul. Mech., 1849, 697 (2015)

[4] Arslan-Alaton I, Aytac E, Kusk KO, Environ. Sci. Pollut. Res., 21, 12122 (2014)

[5] Rivero MJ, Alonso E, Dominguez S, Ribao P, Ibanez R, Ortiz I, Irabien A, J. Chem. Technol. Biotechnol., 89(8), 1228 (2014)

[6] Oller I, Malato S, Sanchez-Perez JA, Sci. Total Environ., 409, 4141 (2011)

[7] Lipczynska-Kochany E, Kochany J, Chemosphere, 73, 745 (2008)

[8] Lindsey ME, Tarr MA, Environ. Sci. Technol., 34, 444 (2000)

[9] Lindsey ME, Tarr MA, Chemosphere, 41, 409 (2000)

[10] Canals M, Gonzalez-Olmos R, Costas M, Company A, Environ. Sci. Technol., 47, 9918 (2013)

[11] ElShafei GMS, Yehia FZ, Dimitry OIH, Badawi AM, Eshaq G, Appl. Catal. B: Environ., 99(1-2), 242 (2010)

[12] Sillanpaa MET, Res. J. Chem. Environ., 13, 99 (2009)

[13] Liu X, Fan JH, Hao Y, Ma LM, Chem. Eng. J., 250, 354 (2014)

[14] Jarand CW, Chen K, Pozniak B, Cole RB, Pham DT, Lincoln SF, Tarr MA, ACS Symp. Ser., 1069, 343 (2011)

[15] Veignie E, Rafin C, Landy D, Fourmentin S, Surpateanu G, J. Hazard. Mater., 168(2-3), 1296 (2009)

[16] Matta R, Hanna K, Kone T, Chiron S, Chem. Eng. J., 144(3), 453 (2008)

[17] Yang CC, Castelvetro V, Scalarone D, Bianchi S, Zhang YM, J. Polym. Sci. A: Polym. Chem., 49(21), 4518 (2011)

[18] Ciobanu A, Ruellan S, Mallard I, Landy D, Gennequin C, Siffert S, Fourmentin S, J. Incl. Phenom. Macrocycl. Chem., 75, 333 (2013)

[19] Benesi HA, Hildebrand JH, J. Am. Chem. Soc (1949).

[20] He PJ, Zheng Z, Zhang H, Shao LM, Tang QY, Sci. Total Environ., 407, 4928 (2009)

[21] Poerschmann J, Trommler U, Gorecki T, Chemosphere, 79, 975 (2010)

[22] Buxton GV, Greenstock CL, Helman WP, Ros AB, J. Phys. Chem. Ref Data, 17, 513 (1988)

[23] Xue XF, Hanna K, Despas C, Wu F, Deng NS, J. Mol. Catal. A-Chem., 311(1-2), 29 (2009)

[24] Yang ZX, Chen Y, Liu Y, Carbohydr. Res., 343, 2439 (2008)

[25] Yang ZX, Zhang X, Cui J, Appl. Catal. B: Environ., 148, 243 (2014)

[26] Vidal RBP, Ibanez GA, Escandar GM, RSC Adv., 5, 20914 (2015)

[27] Liang CJ, Huang CF, Chen YJ, Water Res., 42, 4091 (2008)

[28] Fu L, Zhao Z, Ma J, Hu X, Catal. Commun., 65, 96 (2015)

[29] Zheng W, Tarr MA, Mol. Biomol. Spectrosc., 65, 1098 (2006)

[30] Lindsey ME, Xu G, Lu J, Tarr MA, Sci. Total Environ., 307, 215 (2003)

[31] He J, Yang XF, Men B, Yu L, Wang DS, J. Mol. Catal. A-Chem., 408, 179 (2015)

[32] Peller JR, Mezyk SP, Cooper WJ, Res. Chem. Intermed., 35, 21 (2009)

[33] Huang WY, Brigante M, Wu F, Mousty C, Hanna K, Mailhot G, Environ. Sci. Technol., 47, 1952 (2013)

[34] Peings V, Frayret J, Pigot T, J. Environ. Manage., 157, 287 (2015)

[35] Molkenthin M, Olmez-Hanci T, Jekel MR, Arslan-Alaton I, Water Res., 47, 5052 (2013)

[36] Han Q, Wang HJ, Dong WY, Liu TZ, Yin YL, Fan HK, Chem. Eng. J., 262, 34 (2015)

[37] Zhou YB, Gu XC, Zhang RZ, Lu J, Ind. Eng. Chem. Res., 54(1), 426 (2015)

[38] Luo HY, Liu Y, Yu ZJ, Zhang S, Li BJ, Biomacromolecules, 9(10), 2573 (2008)

[39] Shuai XT, Wei M, Porbeni FE, Bullions TA, Tonelli AE, Biomacromolecules, 3(1), 201 (2002)

[40] Endo H, Nakaji-Hirabayashi T, Morokoshi S, Gemmei-Ide M, Kitano H, Langmuir, 21(4), 1314 (2005)