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Photocatalysis of sulfo and carboxy derivatives of indigo in a TiO2 slurry with the use of polychromatic irradiation

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Abstract

The photocatalytic decomposition of indigo-5,5′-disulfonic acid (indigocarmine) and indigo-6,6′-dicarboxylic acid has been studied using TiO2 suspension and the polychromatic irradiation of a high-pressure Hg arc lamp. The dyestuffs were dissolved in aqueous medium at pH = 10 and photolyzed in a back-flow tubular photoreactor. The reaction products were determined by HPLC, NMR and MS spectroscopy. Two main photoproducts obtained from indigocarmine (2-amino-5-sulfobenzoic acid and isatine-5-sulfonic acid) were detected. The photocatalysis of indigo-6,6′-dicarboxylic acid gave aminoterephthalic acid and isatine-6-carboxylic acid as two main products. The quantitative analyses of reaction products were performed with UV/Vis and HPLC using chemical standards. A stoichiometric model and kinetic description of photocatalysis of sulfo and carboxy indigo dyes are suggested. The effect of hydroxide and carbonate anions on the rate of photocatalysis was also studied.

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References

  1. Saggioro EM, Oliveira AS, Pavesi T, Maia CG, Ferreira LFV, Moreira JC (2011) Molecules 16:10370

    Article  CAS  Google Scholar 

  2. Chen C, Lu C, Chung Y (2006) J Photochem Photobiol A Chem 181:120

    Article  CAS  Google Scholar 

  3. Oliveira AS, Saggioro EM, Barbosa NR, Mazzei A, Ferreira LFV, Moreira JC (2011) Rev Chim 62:462

    CAS  Google Scholar 

  4. Sojić D, Despotović V, Abramović B, Todorova N, Giannakopoulou T, Trapalis C (2010) Molecules 15:2994

    Article  Google Scholar 

  5. Vasapollo G, Mele G, Sole RD, Pio I, Li J, Mazzetto SE (2011) Molecules 16:5769

    Article  CAS  Google Scholar 

  6. Long D (1968) Energy bands in semiconductors. Interscience Publishers, New York

    Google Scholar 

  7. Gonçalves MST, Campos AMFO, Pinto EMMS, Plasencia PMS, Queiroz MJRP (1999) Chemosphere 39:781

    Article  Google Scholar 

  8. Turchi CS, Ollis DF (1990) J Catal 122:178

    Article  CAS  Google Scholar 

  9. Sun L, Bolton JR (1996) J Phys Chem 100:4127

    Article  CAS  Google Scholar 

  10. Vautier M, Guillard C, Hermann J-M (2001) J Catal 201:46

    Article  CAS  Google Scholar 

  11. Vlachopoulos N, Liska P, Augustynski J, Grätzel M (1988) J Am Chem Soc 110:1216

    Article  CAS  Google Scholar 

  12. Kietzmann R, Willig F, Weller H, Vogel R, Nath DN, Eichberger R, Liska P, Lehnert J (1991) Mol Cryst Liq Cryst 194:169

    Article  CAS  Google Scholar 

  13. Spitler M, Calvin M (1976) J Chem Phys 66:4294

    Article  Google Scholar 

  14. Zhang F, Zhao J, Shen T, Hidaka H, Pelizzetti E, Serpone N (1998) Appl Catal B 15:147

    Article  Google Scholar 

  15. Wu G, Wu T, Zhao J, Hidaka H, Serpone N (1999) Environ Sci Technol 33:2081

    Article  Google Scholar 

  16. Liu G, Li X, Zhao J, Horikoshi S, Hidaka H (2000) J Mol Catal A 153:221

    Article  CAS  Google Scholar 

  17. Nguyen T, Ollis DF (1984) J Phys Chem 88:3386

    Article  CAS  Google Scholar 

  18. Ollis DF, Chen-Yung H, Budiman L, Chung-Li Lee (1984) J Catal 88:89

    Article  CAS  Google Scholar 

  19. Ollis DF (1985) Environ Sci Technol 19:480

    Article  CAS  Google Scholar 

  20. Hachem C, Bocquillon F, Zahraa O, Bouchy M (2001) Dyes Pigm 49:117

    Article  CAS  Google Scholar 

  21. Pruden AL, Ollis DF (1983) Environ Sci Technol 17:628

    Article  CAS  Google Scholar 

  22. Cundall RB, Rudham R, Salim M (1976) J Chem Soc Faraday Trans 1:1642

    Google Scholar 

  23. Harvey P, Rudham R, Ward S (1983) J Chem Soc Faraday Trans 1:1381

    Google Scholar 

  24. Harvey P, Rudham R, Ward S (1983) J Chem Soc Faraday Trans 1:2975

    Google Scholar 

  25. Schiavello M, Augugliaro V, Palmisano L (1991) J Catal 127:332

    Article  CAS  Google Scholar 

  26. Martín CA, Baltanás MA, Cassano AE (1996) J Photochem Photobiol A 94:173

    Article  Google Scholar 

  27. Serpone N, Salinaro A (1999) Pure Appl Chem 71:303

    Article  CAS  Google Scholar 

  28. Bailey EJ Jr, Travis J (1985) Dyes Pigm 6:135

  29. National Academy of Sciences (1971) Committee on Food Protection, Food and Nutrition Board, Division of Biology and Agriculture, National Research Council, Food Colors, National Academy of Sciences, Washington DC

  30. Guidelines for Good Manufacturing Practice: Use of Certified FD & C Colors in Food (1968) Food Technol 22:946

    Google Scholar 

  31. Unger J (1956) J Appl Chem 6:245

    Article  Google Scholar 

  32. Maly J, Fadrus H (1966) Cesk Hyg 11:277

    CAS  Google Scholar 

  33. Maly J, Fadrus H (1966) Chem Abstr 65:14429a

    Google Scholar 

  34. Jain BD, Singh JJ (1963) Z Anal Chem 196:89

    Article  CAS  Google Scholar 

  35. Jain BD, Singh JJ (1962) J Less-Common Met 4:145

    Article  CAS  Google Scholar 

  36. Krause A, Slawek J (1969) Fresenius’ Z Anal Chem 244:44

    Article  CAS  Google Scholar 

  37. Ackermann G (1967) Z Chem 7:316

    Article  CAS  Google Scholar 

  38. Bader H, Hoigne J (1981) Water Res 15:449

    Article  CAS  Google Scholar 

  39. Baum K (1978) Schweissen Schneiden 30:439

    CAS  Google Scholar 

  40. Santoro PF, Powell AS (1959) U.S. Atomic Energy Commission, CEND/2401/MD/44, pp 2

  41. Santoro PF, Powell AS (1959) Chem Abstr 57:6607a

    Google Scholar 

  42. Merck WF (1977) Germ Patent 2:742

    Google Scholar 

  43. Merck WF (1977) Chem Abstr 91:2179t

    Google Scholar 

  44. Socha P (1962) Z Urol 55:303

    CAS  Google Scholar 

  45. Deture FA, Drylie DM (1974) J Urol 112:693

    CAS  Google Scholar 

  46. Nelson WL, Ciaccio ET (1961) Anal Biochem 2:39

    Article  CAS  Google Scholar 

  47. Dapson RW, Feldman AT (1980) J Histotechnol 3:138

    Article  CAS  Google Scholar 

  48. Shaw RA, Wylie DW (1967) Sterling-Winthrop Group Ltd., British Patent 1 180957

  49. Shaw RA, Wylie DW (1967) Chem Abstr 73:48541m

    Google Scholar 

  50. Löw W (1885) Chem Ber 18:950

    Google Scholar 

  51. Löw W (1885) Justus Liebegs Ann Chem 231:368

    Google Scholar 

  52. Machalický O, Lichý L, Bad’ura J, Hrdina R, Miranda TM (2006) J Photochem Photobiol A 180:28

    Article  Google Scholar 

  53. Gardecki JA, Maroncelli M (1998) Appl Spectrosc 52:1179

    Article  CAS  Google Scholar 

  54. Cassano AE, Martin CA, Brandi RJ, Alfano OM (1995) Ind Eng Chem Res 34:2155

    Article  CAS  Google Scholar 

  55. Salinaro A, Emeline AV, Zhao J, Hidaka H, Ryabchuk V, Serpone N (1999) Pure Appl Chem 71:321

    Article  CAS  Google Scholar 

  56. Camarero L, Peche R, Merino JM, Rodriguez E (2003) Environ Eng Sci 20(4):281–287

    Article  CAS  Google Scholar 

Download references

Acknowledgments

The support from Research Grant GA104/09/0694, the Czech Republic, is gratefully acknowledged. Authors also thank to Dr. J. Panchartek for careful text revision.

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Correspondence to O. Machalický.

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Machalický, O., Lichý, L., Tomica, M. et al. Photocatalysis of sulfo and carboxy derivatives of indigo in a TiO2 slurry with the use of polychromatic irradiation. Reac Kinet Mech Cat 107, 63–77 (2012). https://doi.org/10.1007/s11144-012-0442-4

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  • DOI: https://doi.org/10.1007/s11144-012-0442-4

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