Iron cycling during the autocatalytic decomposition of benzoic acid derivatives by Fenton-like and photo-Fenton techniques

Applied Catalysis B: Environmental

Volumn 170-171, Issue , 2015, Pages 312-321

  Nichela, Daniela A ^a,c   Donadelli, Jorge A ^a   Caram, Bruno F ^a   Haddou, Ménana ^b   Rodriguez Nieto, Felipe J ^a   Oliveros, Esther ^b   García Einschlag, Fernando S ^a  

^a INSTITUTO DE INVESTIGACIONES FISICOQUÍMICAS TEÓRICAS Y APLICADAS INIFTA   (Argentina)

^b Université Paul Sabatier   (France)

^c LABORATORIO ECOTONO   (Argentina)

Author keywords

Autocatalysis; Benzoic acid derivatives; Hydroxyl radicals; Iron(III) complexation; Iron(III) reduction

Indexed keywords

AROMATIC COMPOUNDS; BENZOIC ACID; CARBOXYLATION; COMPLEXATION; COORDINATION REACTIONS; DEGRADATION; IRON; MOLECULES; OXIDATION; PHENOLS; REACTION INTERMEDIATES;

ALIPHATIC CARBOXYLATE; AUTOCATALYSIS; AUTOCATALYTIC DECOMPOSITIONS; BENZOIC ACID DERIVATIVES; HYDROXYL RADICALS; OXIDATIVE DEGRADATION; PHOTO-FENTON PROCESS; RING OPENING REACTION;

IRON COMPOUNDS;

EID: 84922996859     PISSN: 09263373     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcatb.2015.01.028     Document Type: Article

References (55)

1. Pignatello J.J., Oliveros E., MacKay A. Crit. Rev. Env. Sci. Technol. 2006, 36:1-84.
2. Carlos L., Fabbri D., Capparelli A.L.B.P., Alessandra E., Pramauro, García Einschlag F.S. Chemosphere 2008, 72:952-958.
3. Nichela D., Carlos L., García Einschlag F.S. Appl. Catal. B: Environ. 2008, 82:11-18.
4. Neyens E., Baeyens J. J. Hazard. Mater. 2003, 98:33-50.
5. Malato S., Fernández-Ibáñez P., Maldonado M.I., Blanco J., Gernjak W. Catal. Today 2009, 147:1-59.
6. Nichela D., Haddou M., Benoit-Marquié F., Maurette M.-T., Oliveros E., García Einschlag F.S. Appl. Catal. B: Environ. 2010, 98:171-179.
7. Ohashi Y., Kan Y., Watanabe T., Honda Y., Watanabe T. Org. Biomol. Chem. 2007, 5:840-847.
8. Uchimiya M., Stone A.T. Geochim. Cosmochim. Acta 2006, 70:1388-1401.
9. Rahmawati N., Ohashi Y., Watanabe T., Honda Y., Watanabe T. Biomacromolecules 2005, 6:2851-2856.
10. Pignatello J.J. Environ. Sci. Technol. 1992, 26:944-951.
11. Arslan-Alaton I., Gurses F. J. Photochem. Photobiol. A 2004, 165:165-175.
12. Benkelberg H.-J., Warneck P. J. Phys. Chem. 1995, 99:5214-5221.
13. Catastini C., Sarakha M., Mailhot G., Bolte M. Sci. Total Environ. 2002, 298:219-228.
14. Wang L., Zhang C., Mestankova H., Wu F., Deng N., Pan G., Bolte M., Mailhot G. Photochem. Photobiol. Sci. 2009, 8:1059-1065.
15. Silva M.R.A., Trovó A.G., Nogueira R.F.P. J. Photochem. Photobiol. A 2007, 191:187-192.
16. Ou X., Chen S., Quan X., Zhao H. J. Geochem. Explor. 2009, 102:49-55.
17. Kieber R.J., Hardison D.R., Whitehead R.F., Willey J.D. Environ. Sci. Technol. 2003, 37:4610-4616.
18. Prato-Garcia D., Vasquez-Medrano R., Hernandez-Esparza M. Sol. Energy 2009, 83:306-315.
19. Hug S.J., Laubascher H.-U. Environ. Sci. Technol. 1997, 31:160-170.
20. Zhang C., Wang L., Pan G., Wu F., Deng N., Mailhot G., Mestankova H., Bolte M. J. Hazard. Mater. 2009, 169:772-779.
21. Huang W., Brigante M., Wu F., Hanna K., Mailhot G. J. Photochem. Photobiol. A 2012, 239:17-23.
22. Barbeau K. Photochem. Photobiol. 2006, 82:1505-1516.
23. Rios-Enriquez M., Shahin N., Durán-de-Bazúa C., Lang J., Oliveros E., Bossmann S.H., Braun A.M. Sol. Energy 2004, 77:491-501.
24. Tauler R. Chemometr. Intell. Lab. Sys. 1995, 30:133-146.
25. Garrido M., Larrechi M.S., Rius F.X., Tauler R. Chemometr. Intell. Lab. Sys. 2005, 76:111-120.
26. Garrido M., Lázaro I., Larrechi M.S., Rius F.X. Anal. Chim. Acta 2004, 515:65-73.
27. de Juan A., Tauler R. Anal. Chim. Acta 2003, 500:195-210.
28. Cuesta Sánchez F., Rutan S.C., Gil García M.D., Massart D.L. Chemometr. Intell. Lab. Sys. 1997, 36:153-164.
29. Tauler R., de Juan A. Practical Guide to Chemometrics 2006, 417-467. Taylor & Francis Group, LLC, Greenville. second ed. P. Gemperline (Ed.).
30. Gemperline P.J., Cash E. Anal. Chem. 2003, 75:4236-4243.
31. Nurchi V.M., Pivetta T., Lachowicz J.I., Crisponi G. J. Inorg. Biochem. 2009, 103:227-236.
32. Aydin R., Özer U., Türkel N. Turk. J. Chem. 1997, 21:428-436.
33. Lee K.S., Lee D.W. Anal. Chem. 1974, 46:1903-1908.
34. Hirayama N., Kuwamoto T. Anal. Chem. 1993, 65:141-147.
35. Pozdnyakov I.P., Plyusnin V.F., Grivin V.P., Vorobyev D.Y., Bazhin N.M., Pagés S., Vauthey E. J. Photochem. Photobiol. A 2006, 182:75-81.
36. Gallard H., De Laat J., Legube B. Water Res. 1999, 33:2929-2936.
37. Wu F., Deng N. Chemosphere 2000, 41:1137-1147.
38. Crisponi G., Nurchi V.M., Pivetta T. J. Inorg. Biochem. 2008, 102:209-215.
39. Kawabata T., Schepkin V., Haramaki N., Phadket R., Packer L. Biochem. Pharmacol. 1996, 51:1569-1577.
40. Lopes L., De Laat J., Legube B. Inorg. Chem. 2002, 41:2505-2517.
41. Zuo Y., Hoigné J. Environ. Sci. Technol. 1992, 26:1014-1022.
42. Borer P., Hug S.J., Sulzberger B., Kraeme S.M., Kretzschmar R. J. Phys. Chem. C 2007, 111:10560-10569.
43. David F., David G. J. Phys. Chem. 1976, 80:579-583.
44. Weller C., Horn S., Herrmann H. J. Photochem. Photobiol. A 2013, 268:24-36.
45. Vogler A., Kern A. Z. Naturforsch. B 1979, 34:271-274.
46. Eberson L., Nyberg K. J. Am. Chem. Soc. 1966, 88:1686-1691.
47. Hilborn J., Pincock J. J. Am. Chem. Soc. 1991, 113:2683-2686.
48. Palmisano G., Addamo M., Augugliaro V., Caronna T., Di Paola A., García López E., Loddo V., Marcì G., Palmisano L., Schiavello M. Catal. Today 2007, 122:118-127.
49. Tauber A., Schuchmann H.-P., von Sonntag C. Ultrason. Sonochem. 2000, 7:45-52.
50. Rabaaoui N., Allagui M.S. J. Hazard. Mater. 2012, 243:187-192.
51. Matthews R.W., Sangster D.F. J. Phys. Chem. 1965, 65:1938-1946.
52. Albarra G., Schuler R.H. Radiat. Phys. Chem. 2003, 67:279-285.
53. Xu J., Jordan R.B. Inorg. Chem. 1988, 27:4563-4566.
54. Liu R., Goodell B., Jellison J., Amirbaham A. Environ. Sci. Technol. 2005, 39:175-180.
55. Azrague K., Pradines V., Bonnefille E., Claparols C., Maurette M.-T., Benoit-Marquié F. J. Hazard. Mater. 2012, 237-238:71-78.