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Original Articles

The role of iron species on the turbidity of oxidized phenol solutions in a photo-Fenton system

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Pages 1855-1863 | Received 07 Nov 2014, Accepted 24 Jan 2015, Published online: 05 Mar 2015

References

  • Sprague JB. Measurement of pollutant toxicity to fish I. Bioassay methods for acute toxicity. Wat Res. 1969;3:793–821. doi: 10.1016/0043-1354(69)90050-5
  • Sprague JB. Measurement of pollutant toxicity to fish. II. Utilizing and applying bioassay results. Wat Res. 1970;4:3–32. doi: 10.1016/0043-1354(70)90018-7
  • Santos A, Yustos P, Quintanilla A, García-Ochoa F. Lower toxicity route in catalytic wet oxidation of phenol at basic pH by using bicarbonate media. Appl Cat B Environ. 2004;53(3):181–194. doi: 10.1016/j.apcatb.2004.04.022
  • Ghioureliotis M, Nicell JA. Toxicity of soluble products from the peroxidase-catalysed polymerization of substituted phenolic compounds. J Chem Technol Biotechnol. 2000;75:98–106. doi: 10.1002/(SICI)1097-4660(200001)75:1<98::AID-JCTB181>3.0.CO;2-X
  • Chang YC, Tai KW, Huang FM, Huang MF. Cytotoxic and nongenotoxic effects of phenolic compounds in human pulp cell cultures. J Endod. 2000;26(8):440–443. doi: 10.1097/00004770-200008000-00002
  • Smith CJ, Perfetti TA, Morton MJ, Rodgman A, Garg R, Selassie CD, Hansch C. The relative toxicity of substituted phenols reported in cigarette mainstream smoke. Toxicol Sci. 2002;69(1):265–278. doi: 10.1093/toxsci/69.1.265
  • Lahlou S, Interaminense LF, Magalhães PJ, Leal-Cardoso JH, Duarte GP. Cardiovascular effects of eugenol, a phenolic compound present in many plant essential oils, in normotensive rats. J Cardiovasc Pharm. 2004;43(2):250–257. doi: 10.1097/00005344-200402000-00013
  • Eisenhauer HR. Oxidation of phenolic wastes: I. Oxidation with hydrogen peroxide and a ferrous salt reagent. J Water Pollut Control Fed. 1964;36:1116–1128.
  • Fenton HJH. Oxidation of tartaric acid in the presence of iron. J Chem Soc Trans. 1984;65:889–910.
  • Neyens E, Baeyens J. A review of classic Fenton's peroxidation as an advanced oxidation technique. J Hazard Mater. 2003;98(1–3):33–50. doi: 10.1016/S0304-3894(02)00282-0
  • Villota N, Camarero LM, Lomas JM, Pérez J. Changes of turbidity during the phenol oxidation by photo-Fenton treatment. Environ Sci Pollut Res. 2014;21:12208–12216. doi: 10.1007/s11356-014-3017-2
  • Chevaldonnet C, Cardy H, Dargelos A. Ab initio CI calculations on the PE and VUV spectra of hydrogen peroxide. Chem Phys. 1986;102:55–61. doi: 10.1016/0301-0104(86)85117-5
  • Pignatello JJ, Liu D, Huston P. Evidence for an additional oxidant in the photoassisted Fenton reaction. Environ Sci Technol. 1999;33:1832–1839. doi: 10.1021/es980969b
  • Walling C, Goosen A. Mechanism of the ferric ion catalyzed decomposition of hydrogen peroxide. Effect of organic substrates. J Am Chem Soc. 1973;95:2987–2991. doi: 10.1021/ja00790a042
  • Hynes MJ, O'Coinceanainn M. The kinetics and mechanism of reactions of iron(III) with caffeic acid, chlorogenic acid, sinapic acid, feluric acid and naringin. J Inorg Biochem. 2004;98:1457–1464. doi: 10.1016/j.jinorgbio.2004.05.009
  • Villota N, Mijangos F, Varona F, Andrés J. Kinetic modelling of toxic compounds generated during phenol elimination in wastewaters. Int J Chem React Eng. 2007;5(1):1542–6580.
  • Pignatello JJ. Dark and photoassisted Fe (III)-catalyzed degradation of chlorophenoxy herbicides by hydrogen peroxide. Environ Sci Technol. 1992;26:944–951. doi: 10.1021/es00029a012
  • Gozzo F. Radical and non-radical chemistry of the Fenton-like systems in the presence of organic substrates. J Mol Catal A Chem. 2001;171:1–22. doi: 10.1016/S1381-1169(01)00099-1
  • Hynes MJ, O'Coinceanainn M. The kinetics and mechanisms of the reaction of iron(III) with gallic acid, gallic acid methyl ester and catechin. J Inorg Biochem. 2001;85:131–142. doi: 10.1016/S0162-0134(01)00205-7
  • Yamahara R, Ogo S, Masuda H, Watanabe Y. (Catecholato)iron(III) complexes: structural and functional models for the catechol-bound iron(III) form of catechol dioxygenases. J Inorg Biochem. 2002;88:284–294. doi: 10.1016/S0162-0134(01)00353-1
  • Lindsey ME, Xu G, Lu J, Tarr MA. Enhanced Fenton degradation of hydrophobic organics by simultaneous iron and pollutant complexation with cyclodextrins. Sci Total Environ. 2003;307:215–229. doi: 10.1016/S0048-9697(02)00544-2
  • Chan KH, Chu W. Modeling the reaction kinetics of Fenton's process on the removal of antrazine. Chemosphere. 2003;51:305–311. doi: 10.1016/S0045-6535(02)00812-3
  • Song Y, Xie J, Shu H, Zhao G, Lva X, Caic H. Density-functional theory and ab initio Hartree–Fork studies on the structural parameters and chemical activity of the free radicals generated by benzoquinone and hydroquinone. Bioorg Med Chem. 2005;13:5658–5667. doi: 10.1016/j.bmc.2005.05.029
  • Mijangos F, Varona F, Villota N. Changes in solution color during phenol oxidation by Fenton reagent. Environ Sci Technol. 2006;40:5538–5543. doi: 10.1021/es060866q
  • Rodríguez E, Mimbrero M, Masa FJ, Beltrán FJ. Homogeneous iron-catalyzed photochemical degradation of muconic acid in water. Water Res. 2007;41(6):1325–1333. doi: 10.1016/j.watres.2006.12.007
  • Rodríguez EM, Núñez B, Fernández G, Beltrán FJ. Effects of some carboxylic acids on the Fe(III)/UVA photocatalytic oxidation of muconic acid in water. Appl Catal B Environ. 2009;89(1–2):214–222. doi: 10.1016/j.apcatb.2008.11.030
  • Fortune WB, Mellon MG. Determination of iron with o-phenanthroline. A spectrophotometric study. Ind Eng Chem Anal Ed. 1938;10:60–64. doi: 10.1021/ac50118a004
  • Villota N, Camarero LM, Lomas JM, Legaristi M. Kinetic modelling of photoconversion of phenol by a photo-Fenton reagent and UV. Int J Chem React Eng. 2014;12(1):1542–6580.
  • Zazo JA, Casas JA, Mohedano AF, Gilarranz MA, Rodríguez JJ. Chemical pathway and kinetics of phenol oxidation by Fenton's reagent. Environ Sci Technol. 2005;39:9295–9302. doi: 10.1021/es050452h
  • Devlin HP, Harris IJ. Mechanism of the oxidation of aqueous phenol with dissolved oxygen. Ind Eng Chem Fund. 1984;23:387–392. doi: 10.1021/i100016a002
  • Santos A, Yustos P, Quintanilla A, Rodríguez S, García-Ochoa F. Route of the catalytic oxidation of phenol in aqueous phase. Appl Cat B Environ. 2002;39:97–113. doi: 10.1016/S0926-3373(02)00087-5
  • Friedrich LC, Mendes MA, Oliveira V, Zanta CL, Machulek A, Herbert F. Mechanistic implications of zinc(II) ions on the degradation of phenol by the Fenton reaction. J Braz Chem Soc. 2012;23(7):1372–1377. doi: 10.1590/S0103-50532012000700022
  • Zeng Q, Li Z, Dong L, Han D, Wang R, Li X, Bai G. Remote substituent effects on gas-phase homolytic Fe–O and Fe–S bond energies of p-G-C6H4OFe(CO)2(η5-C5H5) and p-G-C6H4SFe(CO)2(η5-C5H5) studied using Hartree–Fock and density functional theory methods. J Phys Org Chem. 2013;26:664–674. doi: 10.1002/poc.3152
  • Scheck CK, Frimmel FH. Degradation of phenol and salicylic acid by ultraviolet radiation/hydrogen peroxide/oxygen. Wat Res. 1995;29(10):2346–2352. doi: 10.1016/0043-1354(95)00060-X
  • Rasalingam S, Kibombo HS, Wu C-M, Peng R, Baltrusaitis J, Koodali RT. Competitive role of structural properties of titania–silica mixed oxides and a mechanistic study of the photocatalytic degradation of phenol. Appl Catal B Environ. 2014;148–149:394–405. doi: 10.1016/j.apcatb.2013.11.025
  • Mir MH, Vittal JJ. Muconate bridged coordination polymers of Cu(II): effect of auxiliary ligand on their structural architectures. Inorg Chim Acta. 2013;403:97–101. doi: 10.1016/j.ica.2013.01.002
  • Lam SW, Chiang K, Lim TM, Amal R, Low GK-C. The role of ferric ion in the photochemical and photocatalytic oxidation of resorcinol. J Catal. 2005;234:292–299. doi: 10.1016/j.jcat.2005.06.014

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