Photoassisted catalytic cleavage of the C-F bond in pentafluorophenol with ZnO and the effect of operational parameters

Australian Journal of Chemistry

Volumn 60, Issue 12, 2007, Pages 951-956

  Ravichandran, Lakshiminarasimhan ^a   Selvam, Kaliyamoorthy ^b   Swaminathan, Meenakshisundaram ^b  

^a ANNAMALAI UNIVERSITY   (India)

^b Sipcot   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST ACTIVITY; CHEMICAL BONDS; FLUORINE COMPOUNDS; OXIDANTS; PHOTOCATALYSIS; ULTRAVIOLET RADIATION;

DEFLUORIDATION; PENTAFLUOROPHENOL; PHOTOCATALYTIC CLEAVAGE;

AROMATIC COMPOUNDS;

EID: 36749035433     PISSN: 00049425     EISSN: None     Source Type: Journal    
DOI: 10.1071/CH07109     Document Type: Article

References (39)

1. B. D. Key, R. D. Howell, C. S. Griddle, Environ. Sci. Technol. 1997, 31, 2445. doi:10.1021/ES961007C
2. E. Sinclair, S. Taniyasu, N. Yamashita, K. Kannan, Organohalogen Compounds 2004, 66, 4069.
3. K. Kannan, L. Tao, E. Sinclair, S. D. Pastva, D. J. Jude, J. P. Giesy, Arch. Environ. Contam. Toxicol. 2005, 48, 559. doi:10.1007/S00244-004-0133-X
4. K. S. Guruge, S. Taniyasu, N. Yamashita, S. Wijeratna, K. M. Mohotti, H. R. Senevriatne, K. Kannan, N. Yamanaka, S. Miyazaki, J. Environ. Monit. 2005, 7, 371. doi:10.1039/B412532K
5. R. Renner, Environ. Sci. Technol. 2001, 35, 154A.
6. H. Hori, Y. Takano, K. Koike, S. Kutsuna, H. Einaga, T. Ibusuki, Appl. Catal. B: Environ. 2003, 46, 333. doi:10.1016/S0926-3373(03) 00225-X
7. R. Natarajan, R. Azerad, B. Badet, E. Copin, J. Fluorine Chem. 2005, 424. doi:10.1016/J.JFLUCHEM.2004.12.001
8. A. P. New, L. M. Freitas dos Santos, G. L. Biundo, A. Spicq, J. Chromatogr. A 2000, 889, 177. doi:10.1016/S0021-9673(00)00571- 9
9. C. Minero, E. Pelizzetti, Langmuir 1994, 10, 692. doi:10.1021/LA00015A017
10. K. Selvam, M. Muruganandham, M. Swaminathan, Sol. Energy Mater. Sol. Cells 2005, 89, 61. doi:10.1016/J.SOLMAT.2005.01.002
11. M. Muruganandham, M. Swaminathan, Sol. Energy Mater. Sol. Cells 2004, 81, 439. doi:10.1016/J.SOLMAT.2003.11.022
12. M. Muruganandham, M. Swaminathan, Dyes Pigments 2004, 62, 269. doi:10.1016/J.DYEPIG.2003.12.006
13. M. Muruganandham, M. Swaminathan, Dyes Pigments 2004, 63, 315. doi:10.1016/J.DYEPIG.2004.03.004
14. M. Muruganandham, M. Swaminathan, J. Mol. Catal. A: Chem. 2006, 246, 154. doi:10.1016/J.MOLCATA.2005.09.052
15. L. Ravichandran, K. Selvam, M. Muruganandam, M. Swaminathan, J. Fluorine Chem. 2006, 127, 1204. doi:10.1016/JJFLUCHEM.2006.06. 009
16. L. Ravichandran, K. Selvam, M. Muruganandam, M. Swaminathan, J. Photochem. Photobiol. Chem. 2007, 188, 392. doi:10.1016/J.JPHOTOCHEM.2006.12.041
17. D. F. Ollis, Catal. Technol. 1998, 2, 149.
18. M. R. Hoffmann, S. T. Martin, W. Choi, D. W. Bahnemann, Chem. Rev. 1995, 95, 69. doi:10.1021/CR00033A004
19. B. Dindar, S. Icli, J. Photochem. Photobiol. Chem. 2001, 140, 263. doi:10.1016/S1010-6030(01)00414-2
20. M. C. Yeber, J. Roderiguez, J. Freer, J. Baeza, N. Duran, H. D. Mansilla, Chemosphere 1999, 39, 1679. doi:10.1016/S0045-6535(99) 00068-5
21. A. A. Khodja, T. Sheili, J. F. Pihichowski, P. Boule, J. Photochem. Photobiol. Chem. 2001, 141, 231. doi:10.1016/S1010-6030(01) 00423-3
22. N. Serpone, P. Maruthamuthu, P. Pichat, E. Pelizzetti, H. Hidaka, J. Photochem. Photobiol. Chem. 1995, 85, 247. doi:10.1016/1010-6030(94)03906-B
23. T. Hiyama, Organofluorine Compounds: Chemistry and Applications 2000, p. 1 (Springer: Berlin).
24. N. Daneshvar, D. Salari, A. R. Khataee, J. Photochem. Photobiol. Chem. 2004, 162, 317. doi:10.1016/S1010-6030(03)00378-2
25. E. Evgenidou, K. Fytianos, I. Poulios, Appl. Catal. B: Environ. 2005, 59, 81. doi:10.1016/J.APCATB.2005.01.005
26. M. Anpo, T. Shima, Y. Kupakowa, Chem. Lett. (Jpn.) 1985, 1799. doi:10.1246/CL.1985.1799
27. C. D. Jaeger, A. Bard, J. Phys. Chem. 1979, 83, 3146. doi:10.1021/J100487A017
28. Y. Xu, M. A. A. Schoonen, Am. Mineral. 2000, 85, 543.
29. I. A. Alaton, I. A. Balcioglu, D. W. Bahnemann, Water Res. 2002, 36, 1143. doi:10.1016/S0043-1354(01)00335-9
30. P. C. Heimenz, Principle of Colloid and Surface Photochemistry 1986 (Marcel Deckker: New York, NY).
31. L. Wenhua, L. Hong, C. Suo'an, Z. Jianqing, C. Chunan, J. Photochem. Photobiol. Chem. 2000, 131, 125. doi:10.1016/S1010-6030(99) 00232-4
32. D. Chen, A. K. Ray, Water Res. 1998, 32, 3223. doi:10.1016/S0043-1354(98)00118-3
33. G. Galindo, P. Jacques, A. Kalt, Chemosphere 2001, 45, 997. doi:10.1016/S0045-6535(01)00118-7
34. C. Chen, J. C. Chou, Ind. Eng. Chem. Res. 1993, 32, 1520. doi:10.1021/IE00019A028
35. H. Al-Ekabi, N. Serpone, J. Phys. Chem. 1988, 92, 5726. doi:10.1021/J100331A036
36. R. W. Matthews, J. Phys. Chem. 1987, 91, 3328. doi:10.1021/J100296A044
37. D. R. Lide, Handbook of Chemistry and Physics, 76th edn 1995 (CRC Press: London).
38. D. H. Kim, M. A. Anderson, J. Photochem. Photobiol. Chem. 1996, 94, 221. doi:10.1016/1010-6030(95)04178-8
39. K. Okamoto, Y. Yamamoto, H. Tanaka, M. Tanaka, A. Itaya, Bull. Chem. Soc. Jpn. 1985, 58, 2015. doi:10.1246/BCSJ.58.2015