Mechanisms of catalyst action in the TiO2-mediated photocatalytic degradation and cis-trans isomerization of maleic and fumaric acid

Applied Catalysis B: Environmental

Volumn 54, Issue 2, 2004, Pages 105-114

  Oh, Youn Chul ^a   Li, Xiaojing ^a   Cubbage, Jerry W ^a   Jenks, William S ^a  

^a IOWA STATE UNIVERSITY   (United States)

Author keywords

Fumaric acid; Maleic acid; Photocatalytic degradation; Superoxide; Titanium dioxide

Indexed keywords

ADSORPTION; CATALYSTS; ISOMERIZATION; PHOTOCATALYSIS;

ELECTRON TRANSFER; MALEIC ACID; SUPEROXIDES;

TITANIUM OXIDES;

EID: 4644285418     PISSN: 09263373     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcatb.2004.05.024     Document Type: Article

References (80)

1. D.F. Ollis, H. Al-Ekabi (Eds.), Photocatalytic Purification and Treatment of Water and Air, Elsevier, New York, 1993, p. 820.
2. G.R. Helz, R.G. Zepp, D.G. Crosby (Eds.), Aquatic and Surface Photochemistry, Lewis Publishers, Boca Raton, 1994.
3. Bhatkhande D.S., Pangarkar V.G., Beenackers A.A.C.M. J. Chem. Technol. Biotechnol. 77:2002;102
4. Stafford U., Gray K.A., Kamat P.V. Heterog. Chem. Rev. 3:1996;77
5. P.V. Kamat, K. Vinodgopal, in: V. Ramamurthy, Schanze, K., Molecular and Supramolecular Photochemistry: Organic and Inorganic Photochemistry, Marcel Dekker, New York, 1998, p. 307.
6. Hoffmann M.R., Martin S.T., Choi W., Bahnemann D.W. Chem. Rev. 95:1995;69
7. D. Bahnemann, in: P. Boule (Ed.), Handbook of Environmental Chemistry, Springer, Berlin, 1999, p. 285.
8. Mills A., Le Hunte S. J. Photochem. Photobiol. A. 108:1997;1
9. Serpone N. Res. Chem. Intermed. 20:1994;953
10. Hu C., Yu J.C., Hao Z., Wong P.K. Appl. Catal. B. 42:2003;47
11. H. Tada, M. Kubo, Y.-I. Inubushi, S. Ito, Chem. Commun. (2000) 977.
12. Brown G.T., Darwent J.R. J. Chem. Soc., Faraday Trans. 1 Phys. Chem. Condensed Phases. 80:1984;1631
13. Kunitou K., Maeda S., Hongyou S., Mishima K. Canadian J. Chem. Eng. 80:2002;208
14. Tanaka K., Padermpole K., Hisanaga T. Wat. Res. 34:1999;327
15. You D., Xie H., Dai S. J. Environ. Sci. (China). 4:1992;97
16. Muneer M., Bahnemann D. Water Sci. Technol. 44:2001;331
17. Muneer M., Bahnemann D. Appl. Catal. B. 36:2002;95
18. Muneer M., Theurich J., Bahnemann D. J. Photochem. Photobiol. A. 143:2001;213
19. D. Bahnemann, Handbook of Environmental Chemistry, vol. 2, 1999, p. 285.
20. Richard C. New J. Chem. 18:1994;443
21. Richard C., Boule P. New J. Chem. 18:1994;547
22. Richard C., Boule P. Sol. Energy Mater. Sol. Cells. 38:1995;431
23. Theurich J., Lindner M., Bahnemann D.W. Langmuir. 12:1996;6368
24. Li X., Cubbage J.W., Tetzlaff T.A., Jenks W.S. J. Org. Chem. 64:1999;8509
25. Li X., Cubbage J.W., Jenks W.S. J. Org. Chem. 64:1999;8525
26. Bouquet-Somrani C., Finiels A., Graffin P., Olivé J.-L. Appl. Catal. B. 8:1996;101
27. Amalric L., Guillard C., Pichat P. Res. Chem. Intermed. 21:1995;33
28. Pichat P. Water Sci. Technol. 35:1997;73
29. Li X., Cubbage J.W., Jenks W.S. J. Photochem. Photobiol. A. 143:2001;69
30. Tseng J.M., Huang C.P. Water Sci. Technol. 23:1991;377
31. Vulliet E., Emmelin C., Chovelon J.-M., Guillard C., Herrmann J.-M. Appl. Catal. B. 38:2002;127
32. Stylidi M., Kondarides D.I., Verykios X.E. Appl. Catal. B. 40:2003;271
33. Izumi I., Fan F.-R.F., Bard A.J. J. Phys. Chem. 85:1981;218
34. Matthews R.W. J. Chem. Soc., Faraday Trans. 1. 80:1984;457
35. Tahiri H., Ait Ichou Y., Herrmann J.-M. J. Photochem. Photobiol. A. 114:1998;219
36. Prevot A.B., Pramauro E. Talanta. 48:1999;847
37. Assabbane A., Boussaoud A., Albourine A., Aitichou Y., Petit-Ramel M. Ann. Chim. (Paris). 22:1997;301
38. Sakata T., Kawai T., Hashimoto K. J. Phys. Chem. 88:1984;2344
39. Chemseddine A., Boehm H.P. J. Mol. Catal. 60:1990;295
40. Guillard C. J. Photochem. Photobiol. A. 135:2000;65
41. Herrmann J.-M., Tahiri H., Guillard C., Pichat P. Catal. Today. 54:1999;131
42. Sun Y., Pignatello J.J. Environ. Sci. Technol. 29:1995;2065
43. Topalov A., Abramovic B., Molnár-Gábor D., Csanádi J., Arcson O. J. Photochem. Photobiol. A. 140:2001;249
44. Horikoshi S., Hidaka H., Serpone N. J. Photochem. Photobiol. A. 159:2003;289
45. Tanaka K., Reddy K.S.N. Appl. Catal. B. 39:2002;305
46. Trillas M., Peral J., Domenech X. Appl. Catal. B. 5:1995;377
47. Franch M.I., Ayllon J.A., Peral J., Domenech X. Catal. Today. 76:2002;221
48. 2O) δ 3.61 (cis) 3.32 (trans).
49. Payne G.B., Williams P.H. J. Org. Chem. 24:1959;54
50. Hartree E.F. J. Am. Chem. Soc. 75:1953;6244
51. Valentine J.S., Curtis A.B. J. Am. Chem. Soc. 97:1975;224
52. Pedersen C.J., Frensdorff H.K. Angew. Chem. Int. Ed. Engl. 11:1972;16
53. Amalric L., Guillard C., Pichat P. Res. Chem. Int. 20:1994;579
54. Cermenati L., Albini A., Pichat P., Guillard C. Res. Chem. Intermed. 26:2000;221
55. Cermenati L., Pichat P., Guillard C., Albini A. J. Phys. Chem. B. 101:1997;2650
56. Minero C., Mariella G., Maurino V., Vione D., Pelizzetti E. Langmuir. 16:2000;8964
57. Minero C., Mariella G., Maurino V., Pelizzetti E. Langmuir. 16:2000;2632
58. Turchi C.S., Ollis D.F. J. Catal. 122:1990;178
59. Minero C., Catozzo F., Pelizzetti E. Langmuir. 8:1992;481
60. We cite our own work here not out of vanity or because others have not done it, but because we wish to stress that the conditions we are speaking of are identical to those used with other compounds, i.e., done in our hands with our exact procedures.
61. Oh Y.-C., Bao Y., Jenks W.S. J. Photochem. Photobiol. A. 160:2003;69
62. This interpretation is also consistent with our lack of observation of acrylic acid, a product that would likely result from oxidative electron transfer.
63. Kalyanaraman B., Mason R.P., Rowlett R., Kispert L.D. Biochim. Biophys. Acta. 660:1981;102
64. Chang R., Johnson C.S. J. Chem. Phys. 41:1964;3272
65. Johnson C.S., Chang R. J. Chem. Phys. 43:1965;3183
66. Oh Y.-C., Jenks W.S. J. Photochem. Photobiol. A. 162:2004;323
67. As noted in the Experimental section, a different sample holding system was used for these experiments, so the extents of conversions cannot be directly compared to those in Table 1, despite the like irradiation times.
68. Moser J., Punchihewa S., Infelta P.P., Grätzel M. Langmuir. 7:1991;3012
69. Martin S.T., Kesselman J.M., Park D.S., Lewis N.S., Hoffmann M.R. Environ. Sci. Technol. 30:1996;2535
70. Fox M.A., Chen C.C. J. Am. Chem. Soc. 103:1981;6757
71. Araña J., Gonzalez Diaz O., Miranda Saracho M., Dona Rodriguez J.M., Herrera Melian J.A., Perez Pena J. Appl. Catal. B. 36:2002;113
72. Rienstra-Kracofe J.C., Allen W.D., Schaefer H.F.I. J. Phys. Chem. A. 104:2000;9823
73. Stark M.S. J. Am. Chem. Soc. 122:2000;4162
74. Baldwin R.R., Stout D.R., Walker R.W. J. Chem. Soc., Faraday Trans. 87:1991;2147
75. Baker R.R., Baldwin R.R., Fuller A.R., Waker R.W. J. Chem. Soc., Faraday Trans. 1. 71:1975;736
76. Ruiz Diaz R., Selby K., Waddington D.J. J. Chem. Soc., Perkin Trans. 2:1975;758
77. Stothard N.D., Walker R.W. J. Chem. Soc., Faraday Trans. 86:1990;2115
78. Koelewijn P. Recueil. 91:1972;759
79. von Sonntag C., Schuchmann H.-P. Angew. Chem. Int. Ed. Engl. 30:1991;1229
80. Russell G.A. J. Am. Chem. Soc. 79:1957;3871