메뉴 건너뛰기




Volumn 35, Issue 1, 2009, Pages 21-34

Bisphenol A reactions with hydroxyl radicals: Diverse pathways determined between deionized water and tertiary treated wastewater solutions

Author keywords

Bisphenol A; Deionized water; Hydroxyl radical reaction; Tertiary treated wastewaters

Indexed keywords

AROMATIC RINGS; BISPHENOL A; DEGRADATION EFFICIENCY; HYDROXYL RADICAL ADDITION; HYDROXYL RADICAL REACTIONS; HYDROXYL RADICALS; INTERMEDIATE PRODUCT; MECHANISTIC PATHWAYS; OXIDATIVE REACTION; TREATED WASTEWATER; WATER SOLUTIONS;

EID: 77952693850     PISSN: 09226168     EISSN: 15685675     Source Type: Journal    
DOI: 10.1007/s11164-008-0012-6     Document Type: Article
Times cited : (60)

References (33)
  • 1
    • 0032055606 scopus 로고    scopus 로고
    • Identification of alkylphenols and other estrogenic phenolic compounds in wastewater, septage, and groundwater on Cape Cod, Massachusetts
    • R.A. Rudel, S.J. Melly, P.W. Geno, G. Sun, J.G. Brody, Identification of alkylphenols and other estrogenic phenolic compounds in wastewater, septage, and groundwater on Cape Cod, Massachusetts. Environ. Sci. Technol. 32, 861-869 (1998)
    • (1998) Environ. Sci. Technol. , vol.32 , pp. 861-869
    • Rudel, R.A.1    Melly, S.J.2    Geno, P.W.3    Sun, G.4    Brody, J.G.5
  • 2
    • 0035417251 scopus 로고    scopus 로고
    • Determination of endocrine-disrupting phenolic compounds and estrogens in surface and drinking water by HRGC-(NCI)-MS in the picogram per liter range
    • H.M. Kuch, K. Ballschmiter, Determination of endocrine-disrupting phenolic compounds and estrogens in surface and drinking water by HRGC-(NCI)-MS in the picogram per liter range. Environ. Sci. Technol. 35, 3201-3206 (2001)
    • (2001) Environ. Sci. Technol. , vol.35 , pp. 3201-3206
    • Kuch, H.M.1    Ballschmiter, K.2
  • 3
    • 0141621939 scopus 로고    scopus 로고
    • Bisphenol A: Emissions from point sources
    • M. Furhacker, S. Scharf, H. Weber, Bisphenol A: emissions from point sources. Chemosphere 41, 751-756 (2000)
    • (2000) Chemosphere , vol.41 , pp. 751-756
    • Furhacker, M.1    Scharf, S.2    Weber, H.3
  • 4
    • 0035993434 scopus 로고    scopus 로고
    • Occurrence of phthalates and bisphenol A and F in the environment
    • H. Fromme, T. Kuchler, T. Otto, K. Pilz, J. Muller, A. Wenzel, Occurrence of phthalates and bisphenol A and F in the environment. Water Res. 36, 1429-1438 (2002)
    • (2002) Water Res. , vol.36 , pp. 1429-1438
    • Fromme, H.1    Kuchler, T.2    Otto, T.3    Pilz, K.4    Muller, J.5    Wenzel, A.6
  • 5
    • 1842682046 scopus 로고    scopus 로고
    • Environmental fate of bisphenol A and its biological metabolites in river water and their xeno-estrogenic activity
    • T. Suzuki, Y. Nakagawa, I. Takano, K. Yaguchi, Y. Kazuo, Environmental fate of bisphenol A and its biological metabolites in river water and their xeno-estrogenic activity. Environ. Sci. Technol. 38, 2389-2396 (2004)
    • (2004) Environ. Sci. Technol. , vol.38 , pp. 2389-2396
    • Suzuki, T.1    Nakagawa, Y.2    Takano, I.3    Yaguchi, K.4    Kazuo, Y.5
  • 6
    • 34247092973 scopus 로고    scopus 로고
    • Novel estrogen receptor-related transcripts in Marisa cornuarietis; A freshwater snail with reported sensitivity to estrogenic chemicals
    • R. Bannister, N. Beresford, D. May, E.J. Routledge, S. Jobling, M. Rand-Weaver, Novel estrogen receptor-related transcripts in Marisa cornuarietis; a freshwater snail with reported sensitivity to estrogenic chemicals. Environ. Sci. Technol. 41, 2643-2650 (2007)
    • (2007) Environ. Sci. Technol. , vol.41 , pp. 2643-2650
    • Bannister, R.1    Beresford, N.2    May, D.3    Routledge, E.J.4    Jobling, S.5    Rand-Weaver, M.6
  • 8
    • 33845868010 scopus 로고    scopus 로고
    • Exposure to environmentally relevant doses of the xenoestrogen bisphenol-A alters development of the fetal mouse mammary gland
    • L.N. Vandenberg, M.V. Maffini, P.R. Wadia, C. Sonnenschein, B.S. Rubin, A.M. Soto, Exposure to environmentally relevant doses of the xenoestrogen bisphenol-A alters development of the fetal mouse mammary gland. Endocrinology 148, 116-127 (2007)
    • (2007) Endocrinology , vol.148 , pp. 116-127
    • Vandenberg, L.N.1    Maffini, M.V.2    Wadia, P.R.3    Sonnenschein, C.4    Rubin, B.S.5    Soto, A.M.6
  • 9
    • 34249335034 scopus 로고    scopus 로고
    • Prenatal exposure to bisphenol A affects adult murine neocortical structure
    • K. Nakamura, K. Itoh, T. Sugimoto, S. Fushiki, Prenatal exposure to bisphenol A affects adult murine neocortical structure. Neurosci. Lett. 420, 100-105 (2007)
    • (2007) Neurosci. Lett. , vol.420 , pp. 100-105
    • Nakamura, K.1    Itoh, K.2    Sugimoto, T.3    Fushiki, S.4
  • 12
    • 0042238475 scopus 로고    scopus 로고
    • Indirect electrochemical treatment of bisphenol A in water via electrochemically generated Fenton's reagent
    • G. Belgin, M.A. Oturan, N. Oturan, O. Erbatur, Indirect electrochemical treatment of bisphenol A in water via electrochemically generated Fenton's reagent. Environ. Sci. Technol. 37, 3716-3723 (2003)
    • (2003) Environ. Sci. Technol. , vol.37 , pp. 3716-3723
    • Belgin, G.1    Oturan, M.A.2    Oturan, N.3    Erbatur, O.4
  • 13
    • 23844442152 scopus 로고    scopus 로고
    • Transformation and removal of bisphenol A from aqueous phase via peroxidasemediated oxidative coupling reactions: Efficacy, products, and pathways
    • Q. Huang, J. Weber, Transformation and removal of bisphenol A from aqueous phase via peroxidasemediated oxidative coupling reactions: efficacy, products, and pathways. Environ. Sci. Technol. 39, 6029-6036 (2005)
    • (2005) Environ. Sci. Technol. , vol.39 , pp. 6029-6036
    • Huang, Q.1    Weber, J.2
  • 15
    • 29744466516 scopus 로고    scopus 로고
    • Application of slurry type photocatalytic oxidationsubmerged hollow fiber microfiltration hybrid system for the degradation of bisphenol A (BPA)
    • R. Thiruvenkatachari, T.O. Kwon, S. Moon, Application of slurry type photocatalytic oxidationsubmerged hollow fiber microfiltration hybrid system for the degradation of bisphenol A (BPA). Sep. Sci. Technol. 40, 2871-2888 (2005)
    • (2005) Sep. Sci. Technol. , vol.40 , pp. 2871-2888
    • Thiruvenkatachari, R.1    Kwon, T.O.2    Moon, S.3
  • 18
    • 23844496724 scopus 로고    scopus 로고
    • Kinetics of aqueous ozone-induced oxidation of some endocrine disruptors
    • M. Deborde, S. Rabouan, J.-P. Duguet, B. Legube, Kinetics of aqueous ozone-induced oxidation of some endocrine disruptors. Environ. Sci. Technol. 39, 6086-6092 (2005)
    • (2005) Environ. Sci. Technol. , vol.39 , pp. 6086-6092
    • Deborde, M.1    Rabouan, S.2    Duguet, J.-P.3    Legube, B.4
  • 19
    • 4143069310 scopus 로고    scopus 로고
    • Detoxification of bisphenol A and nonylphenol by purified extracellular laccase from a fungus isolated from soil
    • T. Saito, K. Kato, Y. Yokogawa, M. Nishida, N. Yamashita, Detoxification of bisphenol A and nonylphenol by purified extracellular laccase from a fungus isolated from soil. J. Biosci. Bioeng. 98, 64-66 (2004)
    • (2004) J. Biosci. Bioeng. , vol.98 , pp. 64-66
    • Saito, T.1    Kato, K.2    Yokogawa, Y.3    Nishida, M.4    Yamashita, N.5
  • 20
    • 84918833988 scopus 로고
    • Critical review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals (OH/O-) in aqueous solution
    • G. Buxton, C. Greenstock, W.P. Helman, A.B. Ross, Critical review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals (OH/O-) in aqueous solution. J. Phys. Chem. Ref. Data 17, 513-886 (1988)
    • (1988) J. Phys. Chem. Ref. Data , vol.17 , pp. 513-886
    • Buxton, G.1    Greenstock, C.2    Helman, W.P.3    Ross, A.B.4
  • 21
    • 27744601021 scopus 로고    scopus 로고
    • Radiolytic transformations of chlorinated phenols and chlorinated phenoxyacetic acids
    • J. Peller, P.V. Kamat, Radiolytic transformations of chlorinated phenols and chlorinated phenoxyacetic acids. J. Phys. Chem. A 109, 9528-9535 (2005)
    • (2005) J. Phys. Chem. A , vol.109 , pp. 9528-9535
    • Peller, J.1    Kamat, P.V.2
  • 22
    • 0034598859 scopus 로고    scopus 로고
    • Hydroxyl radical reactions with phenol as a model for generation of biologically reactive tyrosyl radicals
    • M.J. Lundqvist, L.A. Eriksson, Hydroxyl radical reactions with phenol as a model for generation of biologically reactive tyrosyl radicals. J. Phys. Chem. B 104, 848-855 (2000)
    • (2000) J. Phys. Chem. B , vol.104 , pp. 848-855
    • Lundqvist, M.J.1    Eriksson, L.A.2
  • 23
    • 33751157922 scopus 로고
    • 2-assisted photocatalytic degradation of 4chlorophenol. A comparative study
    • 2-assisted photocatalytic degradation of 4chlorophenol. A comparative study. J. Phys. Chem. 98, 6343-6351 (1994)
    • (1994) J. Phys. Chem. , vol.98 , pp. 6343-6351
    • Stafford, U.1    Gray, K.2    Kamat, P.V.3
  • 24
    • 0026405450 scopus 로고
    • Pulse radiolytic studies of the reaction of pentahalophenols with OH radicals: Formation of pentahalophenoxyl, dihydroxylpentahalocyclohexadienyl, and semiquinone radicals
    • R. Terzian, N. Serpone, Pulse radiolytic studies of the reaction of pentahalophenols with OH radicals: formation of pentahalophenoxyl, dihydroxylpentahalocyclohexadienyl, and semiquinone radicals. Langmuir 7, 3081-3089 (1991)
    • (1991) Langmuir , vol.7 , pp. 3081-3089
    • Terzian, R.1    Serpone, N.2
  • 26
    • 37049084188 scopus 로고
    • Re-evaluation of the thiocyanate dosimeter for pulse radiolysis
    • G.V. Buxton, C.R. Stuart, Re-evaluation of the thiocyanate dosimeter for pulse radiolysis. J. Chem. Soc. Faraday Trans. 91, 279 (1995)
    • (1995) J. Chem. Soc. Faraday Trans. , vol.91 , pp. 279
    • Buxton, G.V.1    Stuart, C.R.2
  • 27
    • 34948894525 scopus 로고    scopus 로고
    • Free-radical-induced oxidative and reductive degradation of sulfa drugs in water: Absolute kinetics and efficiencies of hydroxyl radical and hydrated electron reactions
    • S.P. Mezyk, T. Neubauer, W.J. Cooper, J.R. Peller, Free-radical-induced oxidative and reductive degradation of sulfa drugs in water: absolute kinetics and efficiencies of hydroxyl radical and hydrated electron reactions. J. Phys. Chem. A 111, 9019-9024 (2007)
    • (2007) J. Phys. Chem. A , vol.111 , pp. 9019-9024
    • Mezyk, S.P.1    Neubauer, T.2    Cooper, W.J.3    Peller, J.R.4
  • 28
    • 0142030625 scopus 로고    scopus 로고
    • Substituent effects in the reaction of OH radicals with aromatics: Toluene
    • G. Albarran, J. Bentley, R.H. Schuler, Substituent effects in the reaction of OH radicals with aromatics: toluene. J. Phys. Chem.A 107, 7770-7774 (2003)
    • (2003) J. Phys. Chem.A , vol.107 , pp. 7770-7774
    • Albarran, G.1    Bentley, J.2    Schuler, R.H.3
  • 29
    • 0031238795 scopus 로고    scopus 로고
    • Mechanisms of ionizing radiation-induced destruction of 2,6-dichlorophenyl in aqueous solutions
    • M. Al-Sheikhly, J. Silverman, P. Neta, L. Karam, Mechanisms of ionizing radiation-induced destruction of 2,6-dichlorophenyl in aqueous solutions. Environ. Sci. Technol. 31, 2473-2477 (1997)
    • (1997) Environ. Sci. Technol. , vol.31 , pp. 2473-2477
    • Al-Sheikhly, M.1    Silverman, J.2    Neta, P.3    Karam, L.4
  • 30
    • 0042238475 scopus 로고    scopus 로고
    • Indirect electrochemical treatment of bisphenol A in water via electrochemically generated Fenton's reagent
    • B. Gozmen, M.A. Oturan, O. Oturan, O. Erbatur, Indirect electrochemical treatment of bisphenol A in water via electrochemically generated Fenton's reagent. Environ. Sci. Technol. 37, 3716-3723 (2003)
    • (2003) Environ. Sci. Technol. , vol.37 , pp. 3716-3723
    • Gozmen, B.1    Oturan, M.A.2    Oturan, O.3    Erbatur, O.4
  • 31
    • 0344359720 scopus 로고    scopus 로고
    • Addition and elimination kinetics in OH radical induced oxidation of phenol and cresols in acidic and alkaline solutions
    • M. Roder, L. Wojnarovits, G. Foldiak, S.S. Emmi, G. Beggiato, M. D'Angelantonio, Addition and elimination kinetics in OH radical induced oxidation of phenol and cresols in acidic and alkaline solutions. Radiat. Phys. Chem. 54, 475-479 (1999)
    • (1999) Radiat. Phys. Chem. , vol.54 , pp. 475-479
    • Roder, M.1    Wojnarovits, L.2    Foldiak, G.3    Emmi, S.S.4    Beggiato, G.5    D'Angelantonio, M.6
  • 32
    • 33847085484 scopus 로고
    • Electrophilic reaction of the OH radical with phenol. Determination of the distribution of isomeric dihydroxycyclohexadienyl radicals
    • N.V. Raghavan, S. Steenken, Electrophilic reaction of the OH radical with phenol. Determination of the distribution of isomeric dihydroxycyclohexadienyl radicals. J. Am. Chem. Soc. 102, 3495-3499 (1980)
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 3495-3499
    • Raghavan, N.V.1    Steenken, S.2
  • 33
    • 0000048953 scopus 로고
    • Aromatic hydroxylation. 8. A radiation chemistry study of the oxidation of hydroxycyclohexadienyl radicals
    • G. Buxton, J.R. Langan, J.R. Smith, Aromatic hydroxylation. 8. A radiation chemistry study of the oxidation of hydroxycyclohexadienyl radicals. J Phys. Chem. 90, 6309-6313 (1986)
    • (1986) J Phys. Chem. , Issue.90 , pp. 6309-6313
    • Buxton, G.1    Langan, J.R.2    Smith, J.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.