Catalytic oxidative degradation of bisphenol A using an ultrasonic-assisted tourmaline-based system: Influence factors and mechanism study

Chemical Engineering Journal

Volumn 252, Issue , 2014, Pages 346-354

  Yu, Li ^a   Wang, Cuiping ^a   Ren, Xinhao ^a   Sun, Hongwen ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

Bisphenol A; Degradation pathway; Kinetics; Surface mechanism; Tourmaline

Indexed keywords

CATALYTIC OXIDATION; DATA HANDLING; ENZYME KINETICS; X RAY PHOTOELECTRON SPECTROSCOPY;

BIS-PHENOL A; DEGRADATION PATHWAYS; FIRST-ORDER KINETIC MODELS; HETEROGENEOUS CATALYST; OPTIMIZED REACTION CONDITIONS; SURFACE MECHANISM; TOURMALINE; ULTRASOUND IRRADIATION;

SILICATE MINERALS;

EID: 84901684426     PISSN: 13858947     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cej.2014.05.014     Document Type: Article

References (69)

1. Huang Y.Q., Wong C.K.C., Zheng J.S., Bouwman H., Barra R., Wahlström B., Neretin L., Wong M.H. Bisphenol A (BPA) in China: a review of sources, environmental levels, and potential human health impacts. Environ. Int. 2012, 42:91-99.
2. Greiner E., Kaelin T., Nakamura K. Chemical Economics Handbook - Bisphenol A 2007, SRI Consulting.
3. Chemical Economics Handbook - Bisphenol A 2010, SRI, SRI Consulting, California.
4. Ballesteros-Gómez A., Rubio S., Pérez-Bendito D. Analytical methods for the determination of bisphenol A in food. J. Chromatogr. A 2009, 1216:449-469.
5. Flint S., Markle T., Thompson S., Wallace E. Bisphenol A exposure, effects, and policy: a wildlife perspective. J. Environ. Manage. 2012, 104:19-34.
6. Zoeller R.T., Bansal R., Parris C. Bisphenol-A, an environmental contaminant that acts as a thyroid hormone receptor antagonist in vitro, increases serum thyroxine, and alters RC3/neurogranin expression in the developing rat brain. Endocrinology 2005, 146:607-612.
7. Gibson R.L. Toxic Baby Bottles: Scientific Study Finds Leaching Chemicals in Clear Plastic Baby Bottles 2007, Environment California Research & Policy Center, Los Angeles.
8. Liu Z., Kanjo Y., Mizutani S. Removal mechanisms for endocrine disrupting compounds (EDCs) in wastewater treatment-physical means, biodegradation, and chemical advanced oxidation: a review. Sci. Total Environ. 2009, 407:731-748.
9. The CRC Handbook of Chemistry and Physics 2001, Chemical Rubber Company, Boca Raton, FL. D.R. Lide (Ed.).
10. Neamtu M., Frimmel F.H. Degradation of endocrine disrupting bisphenol A by 254nm irradiation in different water matrices and effect on yeast cells. Water Res. 2006, 40:3745-3750.
11. 2 photocatalyst. Environ. Sci. Technol. 2001, 35:2365-2368.
12. Deborde M., Rabouan S., Mazellier P., Duguet J.P., Legube B. Oxidation of bisphenol A by ozone in aqueous solution. Water Res. 2008, 42:4299-4308.
13. Li C., Li X., Graham N., Gao N.Y. The aqueous degradation of bisphenol A and steroid estrogens by ferrate. Water Res. 2008, 42:109-120.
14. Inoue M., Masuda Y., Okada F., Sakurai A., Takahashi I., Sakakibara M. Degradation of bisphenol A using sonochemical reactions. Water Res. 2008, 42:1379-1386.
15. Lin S., Gurol M.D. Catalytic decomposition of hydrogen peroxide on iron oxide: kinetics, mechanism, and implications. Environ. Sci. Technol. 1998, 32:1417-1423.
16. Heckert E.G., Seal S., Self W.T. Fenton-like reaction catalyzed by the rare earth inner transition metal cerium. Environ. Sci. Technol. 2008, 42:5014-5019.
17. Katsumata H., Kawabe S., Kaneco S., Suzuki T., Ohta K. Degradation of bisphenol A in water by the photo-Fenton reaction. J. Photochem. Photobiol. A: Chem. 2004, 162:297-305.
18. Rodríguez E.M., Fernández G., Klamerth N., Ignacio Maldonado M., Álvarez P.M., Malato S. Efficiency of different solar advanced oxidation processes on the oxidation of bisphenol A in water. Appl. Catal. B: Environ. 2010, 95:228-237.
19. Torres R.A., Pétrier C., Combet E., Moulet F., Pulgarin C. Bisphenol A mineralization by integrated ultrasound-UV-iron (II) treatment. Environ. Sci. Technol. 2007, 41:297-302.
20. 2 photoassisted process for bisphenol A mineralization. Water Res. 2010, 44:2245-2252.
21. Mohapatra D.P., Brar S.K., Tyagi R.D., Surampalli R.Y. Concomitant degradation of bisphenol A during ultrasonication and Fenton oxidation and production of biofertilizer from wastewater sludge. Ultrason. Sonochem. 2011, 18:1018-1027.
22. Pignatello J.J., Oliveros E., MacKay A. Advanced oxidation processes for organic contaminant destruction based on the Fenton reaction and related chemistry. Crit. Rev. Environ. Sci. Technol. 2006, 36:1-84.
23. Huang H.H., Lu M.C., Chen J.N. Catalytic decomposition of hydrogen peroxide and 2-chlorophenol with iron oxides. Water Res. 2001, 35:2291-2299.
24. Kwan W.P., Voelker B.M. Rates of hydroxyl radical generation and organic compound oxidation in mineral-catalyzed Fenton-like systems. Environ. Sci. Technol. 2003, 37:1150-1158.
25. Matta R., Hanna K., Chiron S. Fenton-like oxidation of 2,4,6-trinitrotoluene using different iron minerals. Sci. Total Environ. 2007, 385:242-251.
26. Neamtu M., Catrinescu C., Kettrup A. Effect of dealumination of iron(III)-exchanged Y zeolites on oxidation of Reactive Yellow 84 azo dye in the presence of hydrogen peroxide. Appl. Catal. B: Environ. 2004, 51:149-157.
27. Iurascu B., Siminiceanu I., Vione D., Vicente M.A., Gil A. Phenol degradation in water through a heterogeneous photo-Fenton process catalyzed by Fe-treated laponite. Water Res. 2009, 43:1313-1322.
28. Yang X., Tian P., Zhang C., Deng Y., Xu J., Gong J., Han Y. Au/carbon as Fenton-like catalysts for the oxidative degradation of bisphenol A. Appl. Catal. B: Environ. 2013, 134-135:145-152.
29. 3 as a reusable heterogeneous Fenton-like catalyst. Environ. Sci. Technol. 2010, 44:1786-1791.
30. 2 composite as an efficient Fenton-Like heterogeneous catalyst for degradation of 4-chlorophenol. Environ. Sci. Technol. 2012, 46:10145-10153.
31. Hu Y., Yang X. The surface organic modification of tourmaline powder by span-60 and its composite. Appl. Surf. Sci. 2012, 258:7540-7545.
32. Yeredla R.R., Xu H. Incorporating strong polarity minerals of tourmaline with semiconductor titania to improve the photosplitting of water. J. Phys. Chem. C 2008, 112:532-539.
33. Wu Z., Wang H., Zheng K., Xue M., Cui P., Tian X. Incorporating strong polarity minerals of tourmaline with carbon nanotubes to improve the electrical and electromagnetic interference shielding properties. J. Phys. Chem. C 2012, 116:12814-12818.
34. Liang J., Wang L., Xu G., Meng J., Ding Y. Far infrared radiation property of rare earth mineral composite materials. J. Rare Earths 2006, 24:281-283.
35. Segura Y., Molina R., Martínez F., Melero J.A. Integrated heterogeneous sono-photo Fenton processes for the degradation of phenolic aqueous solutions. Ultrason. Sonochem. 2009, 16:417-424.
36. Rubert K.F., Pedersen J.A. Kinetics of oxytetracycline reaction with a hydrous manganese oxide. Environ. Sci. Technol. 2006, 40:7216-7221.
37. Weber W.J. Environmental Systems and Processes: Principles, Modeling, and Design 2001, Wiley-Interscience, New York.
38. Breitbach M., Bathen D. Influence of ultrasound on adsorption processes. Ultrason. Sonochem. 2001, 8:277-283.
39. Hamdaoui O., Naffrechoux E., Suptil J., Fachinger C. Ultrasonic desorption of p-chlorophenol from granular activated carbon. Chem. Eng. J. 2005, 106:153-161.
40. Neppolian B., Park J.S., Choi H. Effect of Fenton-like oxidation on enhanced oxidative degradation of para-chlorobenzoic acid by ultrasonic irradiation. Ultrason. Sonochem. 2004, 11:273-279.
41. Zhang H., Fu H., Zhang D. Degradation of C.I. Acid Orange 7 by ultrasound enhanced heterogeneous Fenton-like process. J. Hazard. Mater. 2009, 172:654-660.
42. 4 magnetic nanoparticles under neutral condition. Chem. Eng. J. 2012, 197:242-249.
43. Xu H., Prasad M., Liu Y. Schorl: a novel catalyst in mineral-catalyzed Fenton-like system for dyeing wastewater discoloration. J. Hazard. Mater. 2009, 165:1186-1192.
44. Teel A.L., Warberg C.R., Atkinson D.A., Watts R.J. Comparison of mineral and soluble iron Fenton's catalysts for the treatment of trichloroethylene. Water Res. 2001, 35:977-984.
45. Andreozzi R., D'Apuzzo A., Marotta R. Oxidation of aromatic substrates in water/goethite slurry by means of hydrogen peroxide. Water Res. 2002, 36:4691-4698.
46. Rusevova K., Kopinke F.D., Georgi A. Nano-sized magnetic iron oxides as catalysts for heterogeneous Fenton-like reactions - influence of Fe(II)/Fe(III) ratio on catalytic performance. J. Hazard. Mater. 2012, 241-242:433-440.
47. Hanna K., Kone T., Medjahdi G. Synthesis of the mixed oxides of iron and quartz and their catalytic activities for the Fenton-like oxidation. Catal. Commun. 2008, 9:955-959.
48. Watts R.J., Foget M.K., Kong S.H., Teel A.L. Hydrogen peroxide decomposition in model subsurface systems. J. Hazard. Mater. 1999, 69:229-243.
49. Masomboon N., Ratanatamskul C., Lu M.C. Kinetics of 2,6-dimethylaniline oxidation by various Fenton processes. J. Hazard. Mater. 2011, 192:347-353.
50. Feng J., Hu X., Yue P.L. Discoloration and mineralization of orange II using different heterogeneous catalysts containing Fe: a comparative study. Environ. Sci. Technol. 2004, 38:5773-5778.
51. Melero J.A., Martinez F., Molina R. Effect of ultrasound on the properties of heterogeneous catalysts for sono-Fenton oxidation processes. J. Adv. Oxid. Technol. 2008, 11:75-83.
52. Xia M., Hu C., Zhang H. Effects of tourmaline addition on the dehydrogenase activity of Rhodopseudomonas palustris. Process Biochem. 2006, 41:221-225.
53. Lipczynska-Kochany E. Hydrogen peroxide mediated photodegradation of phenol as studied by a flash photolysis/HPLC technique. Environ. Pollut. 1993, 80:147-152.
54. Reisz E., Schmidt W., Schuchmann H.P., von Sonntag C. Photolysis of ozone in aqueous solutions in the presence of tertiary butanol. Environ. Sci. Technol. 2003, 37:1941-1948.
55. Kitajima N., Fukuzumi S.I., Ono Y. Formation of superoxide ion during the decomposition of hydrogen peroxide on supported metal oxides. J. Phys. Chem. 1978, 82:1505-1509.
56. Suter D., Banwart S., Stumm W. Dissolution of hydrous iron (III) oxides by reductive mechanisms. Langmuir 1991, 7:809-813.
57. Zinder B., Furrer G., Stumm W. The coordination chemistry of weathering: II. Dissolution of Fe(III) oxides. Geochim. Cosmochim. Acta 1986, 50:1861-1869.
58. Segal M.G., Sellers R.M. Reactions of solid iron (III) oxides with aqueous reducing agents. J. Chem. Soc., Chem. Commun. 1980, 21:991-993.
59. Manceau A., Lanson B., Drits V.A., Chateigner D., Gates W.P., Wu J., Huo D., Stucki J.W. Oxidation-reduction mechanism of iron in dioctahedral smectites: I. Crystal chemistry of oxidized reference nontronites. Am. Mineral. 2000, 85:133-152.
60. Handler R.M., Beard B.L., Johnson C.M., Scherer M.M. Atom exchange between aqueous Fe(II) and goethite: an Fe isotope tracer study. Environ. Sci. Technol. 2009, 43:1102-1107.
61. Gorski C.A., Scherer M.M. Influence of magnetite stoichiometry on Fe(II) uptake and nitrobenzene reduction. Environ. Sci. Technol. 2009, 43:3675-3680.
62. Yanina S.V., Rosso K.M. Linked reactivity at mineral-water interfaces through bulk crystal conduction. Science 2008, 320:218-222.
63. Williams A.G.B., Scherer M.M. Spectroscopic evidence for Fe(II)-Fe(III) electron transfer at the iron oxide-water interface. Environ. Sci. Technol. 2004, 38:4782-4790.
64. Schaefer M.V., Gorski C.A., Scherer M.M. Spectroscopic evidence for interfacial Fe(II)-Fe(III) electron transfer in a clay mineral. Environ. Sci. Technol. 2011, 45:540-545.
65. Wang C., Wang B., Liu J., Yu L., Sun H., Wu J. Adsorption of Cd(II) from acidic aqueous solutions by tourmaline as a novel material. Chin. Sci. Bull. 2012, 57:3218-3225.
66. Lin K., Liu W., Gan J. Oxidative removal of bisphenol A by manganese dioxide: efficacy, products, and pathways. Environ. Sci. Technol. 2009, 43:3860-3864.
67. Zhan M., Yang X., Xian Q., Kong L. Photosensitized degradation of bisphenol A involving reactive oxygen species in the presence of humic substances. Chemosphere 2006, 63:378-386.
68. Poerschmann J., Trommler U., Górecki T. Aromatic intermediate formation during oxidative degradation of bisphenol A by homogeneous sub-stoichiometric Fenton reaction. Chemosphere 2010, 79:975-986.
69. Spivack J., Leib T.K., Lobos J.H. Novel pathway for bacterial metabolism of bisphenol A: rearrangements and stilbene cleavage in bisphenol A metabolism. J. Biol. Chem. 1994, 269:7323-7329.