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Volumn 54, Issue 8, 2004, Pages 1207-1215

Photochemical degradation of selected nitropolycyclic aromatic hydrocarbons in solution and adsorbed to solid particles

Author keywords

Nitro group orientation; Nitropolycyclic aromatic hydrocarbons; Photodegradation

Indexed keywords

ADSORPTION; ALUMINA; CELLULOSE; IRRADIATION; PHOTODEGRADATION; SILICA; STRUCTURE (COMPOSITION); SURFACE PHENOMENA;

EID: 1642517118     PISSN: 00456535     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2003.09.020     Document Type: Article
Times cited : (37)

References (20)
  • 1
    • 0000290949 scopus 로고
    • Oxidation of polynuclear aromatic hydrocarbons with ceric ammonium sulfate: Preparation of quinones and lactones
    • Balanikas, G., Hussain, N., Amin, S., Hecht, S.S., 1988. Oxidation of polynuclear aromatic hydrocarbons with ceric ammonium sulfate: preparation of quinones and lactones. J. Org. Chem. 53 (5), 1007-1010.
    • (1988) J. Org. Chem. , vol.53 , Issue.5 , pp. 1007-1010
    • Balanikas, G.1    Hussain, N.2    Amin, S.3    Hecht, S.S.4
  • 2
    • 20244371230 scopus 로고
    • Vibrational spectra of bromotetracarbonyl nitrosyltungsten(I)
    • Butler, I.S., Shaw III, C.F., 1975. Vibrational spectra of bromotetracarbonyl nitrosyltungsten(I). J. Raman Spectrosc. 3 (1), 65-71.
    • (1975) J. Raman Spectrosc. , vol.3 , Issue.1 , pp. 65-71
    • Butler, I.S.1    Shaw III, C.F.2
  • 3
    • 33947336646 scopus 로고
    • Photochemical transformations. XVII. Photochemical studies on 9-nitroanthracene
    • Chapman, O.L., Heckert, D.C., Reasoner, J.W., Thackaberry, S.P., 1966. Photochemical transformations. XVII. Photochemical studies on 9-nitroanthracene. J. Am. Chem. Soc. 88 (23), 5550-5554.
    • (1966) J. Am. Chem. Soc. , vol.88 , Issue.23 , pp. 5550-5554
    • Chapman, O.L.1    Heckert, D.C.2    Reasoner, J.W.3    Thackaberry, S.P.4
  • 4
    • 0000235491 scopus 로고
    • Synthesis and conformational analysis of nitropolycyclic fluoranthenes
    • Cho, B.P., Kim, M., Harvey, R.G.J., 1993. Synthesis and conformational analysis of nitropolycyclic fluoranthenes. J. Org. Chem. 58 (21), 5788-5796.
    • (1993) J. Org. Chem. , vol.58 , Issue.21 , pp. 5788-5796
    • Cho, B.P.1    Kim, M.2    Harvey, R.G.J.3
  • 5
    • 0030111594 scopus 로고    scopus 로고
    • Photostability of nitro-polycyclic aromatic hydrocarbons on combustion soot particles in sunlight
    • Fan, Z., Kamens, R.M., Hu, J., Zhang, J., McDow, S., 1996. Photostability of nitro-polycyclic aromatic hydrocarbons on combustion soot particles in sunlight. Environ. Sci. Technol. 30 (4), 1358-1364.
    • (1996) Environ. Sci. Technol. , vol.30 , Issue.4 , pp. 1358-1364
    • Fan, Z.1    Kamens, R.M.2    Hu, J.3    Zhang, J.4    McDow, S.5
  • 6
    • 0032912954 scopus 로고    scopus 로고
    • Nitro-polycyclic aromatic hydrocarbons: A class of genotoxic environmental pollutants
    • Fu, P.P., Herreno-Saenz, D., 1999. Nitro-polycyclic aromatic hydrocarbons: a class of genotoxic environmental pollutants. Environ. Carcinog. Ecotoxicol. Rev. C 17 (1), 1-43.
    • (1999) Environ. Carcinog. Ecotoxicol. Rev. C , vol.17 , Issue.1 , pp. 1-43
    • Fu, P.P.1    Herreno-Saenz, D.2
  • 7
    • 0021811197 scopus 로고
    • The orientation of the nitro substituent predicts the direct-acting bacterial mutagenicity of nitrated polycyclic aromatic hydrocarbons
    • Fu, P.P., Chou, M.W., Miller, D.W., White, G.L., Heflich, R.H., Beland, F.A., 1985. The orientation of the nitro substituent predicts the direct-acting bacterial mutagenicity of nitrated polycyclic aromatic hydrocarbons. Mutat. Res. 143, 173-181.
    • (1985) Mutat. Res. , vol.143 , pp. 173-181
    • Fu, P.P.1    Chou, M.W.2    Miller, D.W.3    White, G.L.4    Heflich, R.H.5    Beland, F.A.6
  • 8
    • 0041287655 scopus 로고
    • Separation and characterization of mononitro derivatives of benzo(a)pyrene, benzo(e)pyrene and benzo[ghi]perylene
    • Johansen, E., Sydnes, L.K., Greibrokk, T., 1984. Separation and characterization of mononitro derivatives of benzo(a)pyrene, benzo(e)pyrene and benzo[ghi]perylene. Acta Chem. Scand. B 38, 309-318.
    • (1984) Acta Chem. Scand. B , vol.38 , pp. 309-318
    • Johansen, E.1    Sydnes, L.K.2    Greibrokk, T.3
  • 9
    • 0025779868 scopus 로고
    • Nitro group orientation, reduction potential, and direct-acting mutagenicity of nitro-polycyclic aromatic hydrocarbons
    • Jung, H., Shaikh, A.U., Heflich, R.H., Fu, P.P., 1991. Nitro group orientation, reduction potential, and direct-acting mutagenicity of nitro-polycyclic aromatic hydrocarbons. Environ. Mol. Mutagen. 17, 169-180.
    • (1991) Environ. Mol. Mutagen. , vol.17 , pp. 169-180
    • Jung, H.1    Shaikh, A.U.2    Heflich, R.H.3    Fu, P.P.4
  • 10
    • 0018842602 scopus 로고
    • Oxidative transformations of polycyclic aromatic hydrocarbons adsorbed on coal fly ash
    • Korfmacher, W.A., Natusch, D.F.S., Taylor, D.R., Mamantov, G., Wehry, E.L., 1980. Oxidative transformations of polycyclic aromatic hydrocarbons adsorbed on coal fly ash. Science 207, 763-765.
    • (1980) Science , vol.207 , pp. 763-765
    • Korfmacher, W.A.1    Natusch, D.F.S.2    Taylor, D.R.3    Mamantov, G.4    Wehry, E.L.5
  • 11
    • 0034609424 scopus 로고    scopus 로고
    • The conformation of some nitro-polycyclic aromatic hydrocarbons
    • Li, Y.S., Fu, P.P., Church, J.S., 2000. The conformation of some nitro-polycyclic aromatic hydrocarbons. J. Mol. Struct. 550-551, 217-223.
    • (2000) J. Mol. Struct. , vol.550-551 , pp. 217-223
    • Li, Y.S.1    Fu, P.P.2    Church, J.S.3
  • 12
    • 0013195310 scopus 로고    scopus 로고
    • Mass spectral analysis of nitropolycyclic aromatic hydrocarbons with torsion angles obtained from semiempirical calculations
    • Lin, S.-T., Jih, Y.-F., Fu, P.P., 1996. Mass spectral analysis of nitropolycyclic aromatic hydrocarbons with torsion angles obtained from semiempirical calculations. J. Org. Chem. 61, 5271-5273.
    • (1996) J. Org. Chem. , vol.61 , pp. 5271-5273
    • Lin, S.-T.1    Jih, Y.-F.2    Fu, P.P.3
  • 13
    • 0002805072 scopus 로고
    • Effect of a nitro group geometry on the proton NMR chemical shifts of nitro aromatics
    • Miller, D.W., Evans, F.E., Fu, P.P., 1985. Effect of a nitro group geometry on the proton NMR chemical shifts of nitro aromatics. Spectrosc. Int. J. 4 (2), 91-94.
    • (1985) Spectrosc. Int. J. , vol.4 , Issue.2 , pp. 91-94
    • Miller, D.W.1    Evans, F.E.2    Fu, P.P.3
  • 15
    • 0020579803 scopus 로고
    • Mutagenicity and genotoxicity of nitroarenes. All nitro-containing chemicals are not created equal
    • Rosenkranz, H.S., Mermelstein, R., 1983. Mutagenicity and genotoxicity of nitroarenes. All nitro-containing chemicals are not created equal. Mutat. Res. 114, 217-267.
    • (1983) Mutat. Res. , vol.114 , pp. 217-267
    • Rosenkranz, H.S.1    Mermelstein, R.2
  • 16
    • 0007797746 scopus 로고
    • The crystal structure of some anthracene derivatives. V. 9-Nitroanthracene
    • Trotter, J., 1959. The crystal structure of some anthracene derivatives. V. 9-nitroanthracene. Acta Cryst. 12, 237-242.
    • (1959) Acta Cryst. , vol.12 , pp. 237-242
    • Trotter, J.1
  • 17
    • 0003613758 scopus 로고
    • The crystal structure of 1,5-dinitronaphthalene
    • Trotter, J., 1960. The crystal structure of 1,5-dinitronaphthalene. Acta Cryst. 13, 95-99.
    • (1960) Acta Cryst. , vol.13 , pp. 95-99
    • Trotter, J.1
  • 19
    • 84954810418 scopus 로고
    • Photodecomposition of environmental nitro-polycyclic aromatic hydrocarbons
    • Yang, D.T.C., Chou, A., Chen, E., Chiu, L.-H., Ni, Y., 1994. Photodecomposition of environmental nitro-polycyclic aromatic hydrocarbons. Polycyclic Aromat. Compd. 5, 201-208.
    • (1994) Polycyclic Aromat. Compd. , vol.5 , pp. 201-208
    • Yang, D.T.C.1    Chou, A.2    Chen, E.3    Chiu, L.-H.4    Ni, Y.5
  • 20
    • 0012943915 scopus 로고
    • Formation of 1-nitro-2-hydroxypyrene from 1-nitropyrene by photolysis
    • Yasuhara, A., Fuwa, K., 1983. Formation of 1-nitro-2-hydroxypyrene from 1-nitropyrene by photolysis. Chem. Lett., 347-348.
    • (1983) Chem. Lett. , pp. 347-348
    • Yasuhara, A.1    Fuwa, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.