Modulating the Oxidation of FMNH2 by Organophosphorus Compounds

Journal of Advanced Oxidation Technologies

Volumn 11, Issue 3, 2008, Pages 455-462

  Guo, Wen ^a   Ciptadjaya, Christopher G E ^b   Liu, Minghong ^a   Simms, Catherine M ^b   Obare, Sherine O ^a,b  

^a UNIVERSITY OF NORTH CAROLINA AT CHARLOTTE   (United States)

^b WESTERN MICHIGAN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONDUCTION BANDS; FREE RADICAL REACTIONS; METHANOL; NANOCRYSTALS; PHOSPHORUS COMPOUNDS; TITANIUM DIOXIDE;

CONDUCTION BAND ELECTRONS; ELECTRON TRANSFER; ENVIRONMENTAL FACTORS; FENTHION; NANOCRYSTALLINE TIO2; ORGANOPHOSPHORUS COMPOUNDS; PHOTO-REDUCTION; SEMIQUINONE RADICALS;

ORGANIC SOLVENTS;

EID: 63049140008     PISSN: 12038407     EISSN: None     Source Type: Journal    
DOI: 10.1515/jaots-2008-0304     Document Type: Article

References (36)

1. Coats, J. R. Chemtech. 1993, 25-29.
2. Liu, G.; Lin, Y. Anal. Chem. 2005, 77(18), 5894-5901.
3. Gilliom, R. J.; Barbash, J. E.; Kolpin, D. W.; Larson, S. J. Environ. Sci. Technol. 1999, 33(7), 164A-169A
4. United States Geological Survey. Organophosphorous pesticides occurrence and distribution in surface and ground water of the United States; 1992-1997; 2000; pp 1-4.
5. Holland, P. T.; Malcolm, C. P., Multiresidue analysis of fruit and vegetables. In Emerging Strategies for Pesticide Analysis, Cairns, T.; Sherma, J., Eds. CRC Press: 1992; pp 71.
6. Coates, J. R. In Pesticide Transformation Products: Fate and Significance in the Environment, ACS Symposium Series 459; American Chemical Society, Washington, D. C., 1991;
7. Somasundaram, L.; Coates, J. R., Eds. Washington, D. C, 1991, 10.
8. Han, X.; Balakrishnan, V. K.; vanLoon, G. W.; Buncel, E. Langmuir 2006, 22, 9009-9017.
9. Balakrishnan, V. K.; Buncel, E.; VanLoon, G. W. Environ. Sci. Technol. 2005, 39, 5824-5830.
10. Fujisawa, T.; Katagi, T. J. Pest. Sci. 2005, 30(2), 103-110.
11. 10) Horne, I.; Sutherland, T. D.; Harcourt, R. L.; Russell, R. J.; Oakeshott, J. G. Appl. Environ. Microbiol. 2002, 68, 3371-3376.
12. hang J. L., Qiao, C. L, Int. J. Environ. Pollut. 2002, 18, 423-443.
13. Bhadbhade, B. J.; Sarnaik, S. S.; Kanekar, P. P. J. Appl. Microbiol. 2002, 93(2), 224-234.
14. Goncalves, C.; Dimou, A.; Sakkas, V.; Alpendurada, M. F.; Albanis, T. A. Chemosphere 2006, 64, 1375-1382.
15. Keum, Y. S.; Li, Q. X. Chemosphere 2004, 54, 255-263.
16. Sakkas, V. A.; Lambropoulou, D. A.; Sakellarides, T. M.; Albanis, T. A. Anal. Chim. Acta. 2002, 467, 233-243.
17. Li, L.; Wu, Q. Y.; Guo, Y. H.; Hu, C. W. Micropor. Mesopor. Mater. 2005, 87, 1-9.
18. Daneshvar, N.; Hejazi, M. J.; Rangarangy, B.; Khataee, A. R. J. Environ. Sci. Health B. 2004, 39(2), 285-296.
19. Chanda, A.; Khetan, S. K.; Banerjee, D.; Ghosh, A.; Collins, T. J. J. Am. Chem. Soc. 2006, 128, 12058-12059.
20. Zamy, C.; Mazellier, P.; Legube, B. Water Research 2004, 38, 2305-2314.
21. Franko, M.; Sarakha, M.; Cibej, A; Boskin, A.; Bavcon, M.; Trebse, P. Pure Appl. Chem. 2005, 77, 1727-1736.
22. Evgenidou, E.; Konstantinou, I.; Fytianos, K.; Poulios, I. Water Research 2007, 41, 2015-2027.
23. Zayats, M.; Katz, E.; Willner, I. J. Am. Chem. Soc. 2002,124, 2120-2121.
24. Willner, I.; Blonder, R.; Katz, E. J. Am. Chem. Soc. 1996, 118, 5310-5311.
25. Blonder, R.; Katz, E.; Willner, I.; Wray, V.; Buckmann, A. F. J. Am. Chem. Soc. 1997, 119, 11747-11757.
26. Blonder, R.; Willner, I.; Buckmann, A. F. J. Am. Chem. Soc. 1998, 120, 9335-9341.
27. Willner, I.; Heleg-Shabtai, V.; Blonder, R.; Katz, E.; Tao, G. J. Am. Chem. Soc. 1996, 118, 10321-10322.
28. Walsh, C. Acc. Chem. Res. 1980, 18, 148-155.
29. Ghisla, S.; Massey, V.; Lhoste, J. M.; Mayhew, S. G. Biochem. 1974, 13, 589-597.
30. Totten, L. A.; Roberts, A. L. Critical Review Environmental Science and Technology 2001, 31, 175-221.
31. Nakhle, B. M.; Trammell, S. A.; Sigel, K. M.; Meyer, T. J.; Erickson, B. W. Tetrahedron 1999, 55, 2835-2846.
32. Langmuir, I. J. Am. Chem. Soc. 1918, 40, 1316.
33. Trammell, S. A.; Meyer, T. J. J. Phys. Chem. B. 1999, 103(1), 104-107.
34. Obare, S. O.; Ito, T.; Meyer, G. J. Environ. Sci. & Technol. 2005, 39, 6266-6272.
35. It is well known that phosphates have a tendency to bind to metal oxide surfaces such as TiO2. To assess whether the OP compounds investigated in this study could bind to the TiO2 surface, we prepared known concentrations of either ethion, fenthion, or DCP. We immersed a TiO2 slide in each of the solutions, and after 24 hours removed the slide and measured the concentration of each of the OP compounds. In each case, there is loss in the concentration of the OP compound (assessed by UV-visible absorbance or GC-MS analysis of the solution after the TiO2 slide was removed), which suggests that some of the compound may be adsorbed to the TiO2 surface. On the other hand, comparable experiments conducted with FMN functionalized TiO2 showed no significant changes in the concentration of any of the OP pesticides.
36. 35) Obare, S. O.; Ito, T.; Meyer, G. J. J. Am. Chem. Soc. 2006, 128, 712-713.