Abstract
When a dilute aqueous solution (100 ppm) of pentachlorophenol (PCP) was irradiated with sunlight or UV light, the photodegradation products were found to be chlorinated phenols, tetrachlorodihydroxyl benzenes and non-aromatic fragments such as dichloromaleic acid. Subsequent irradiation of the tetrachlorodiols resulted in the formations of hydroxylated trichlorobenzoquinones, trichlorodiols, dichloromaleic acid and non-aromatic fragments. Dichloromaleic acid, when irradiated, produced chloride ions and carbon dioxide. Prolonged irradiation of PCP or its photodegradation products yielded colorless solutions containing no ether-extractable volatile materials; and evaporation of the aqueous layer left no observable polymeric residue such as humic acid. Octachlorodibenzo-p-dioxin was formed when a high concentration of the sodium salt of PCP was irradiated.
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References
Bevenue, A., and H. Beckman, 1967. Pentachlorophenol: A discussion of its properties and its occurrence as a residue in human and animal tissues. Residue Rev., 19: 83–134.
Crosby, D.G., K.W. Moilanen, M. Nakagawa, and A.S. Wong, 1972. Photonucleophilic reactions of pesticides. In, Environmental Toxicology of Pesticides, pp. 423–431 ( F. Matsumura, G.M. Boush, and T. Misato, Eds.). Academic Press, New York. pp. 423–431.
Crosby, D.G., A.S. Wong, J.R. Plimmer, and E.A. Woolson, 1971. Photodecomposition of chlorinated dibenzo-p-dioxins. Science, 173: 748–749.
Crosby, D.G., and A.S. Wong, 1973a. Photodecomposition of p-chlorophenoxyacetic acid. J. Agr. Food Chem., 21: 1049–1052.
Crosby, D.G., and A.S. Wong, 1973b. Photodecomposition of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) in water. J. Agr. Food Chem., 21: 1052–1054.
Crosby, D.G., and A.S. Wong, 1976. Photochemical generation of chlorinated dioxins. Chemosphere, 5: 327–332.
Hamadmad, N., 1967. Photolysis of pentachloronitrobenzene, 2,3,5,6-tetrachloronitro-benzene, and pentachlorophenol. Ph.D. Dissertation, Univ. of California, Davis, California, 93 p.
Karrer, P., and E. Testa, 1949. Oxydatives Abbau des Tetrachloro-o-benzothinons mit Perphtalsaure. Untersuchung der Oxydationsprodukte. Helv. Chim. Acta, 32: 1019–1028.
Kuwahara, M., N. Kato, and K. Munakata, 1966a. The photochemical reaction of pentachlorophenol. Part I. The structure of the yellow compound. Agr. Biol. Chem., Japan, 30: 232–238.
Kuwahara, M., N. Kato, and K. Munakata, 1966b. The photochemical reaction of pentachlorophenol. Part II. The chemical structure of minor products. Agr. Biol. Chem., Japan, 30: 239–245.
Omura, K., and T. Matsura, 1969. Photolysis of halogeno-phenols in aqueous alkali and cyanide. Chem. Commun., 1394–1395.
von Rumker, R., W. Lawless, and A.F. Meiners, 1974. Production, Distribution, Use and Environmental Impact Potential of Selected Pesticides. Office of Pesticide Programs, Environmental Protection Agency, Washington, D.C. 439 p.
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© 1978 Plenum Press, New York
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Crosby, D.G., Wong, A.S. (1978). Photolysis of Pentachlorophenol in Water. In: Rao, K.R. (eds) Pentachlorophenol. Environmental Science Research, vol 12. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-8948-8_3
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DOI: https://doi.org/10.1007/978-1-4615-8948-8_3
Publisher Name: Springer, Boston, MA
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