Dioxin and dioxin-like PCB impurities in some Japanese agrochemical formulations

被引:188
作者
Masunaga, S
Takasuga, T
Nakanishi, J
机构
[1] Yokohama Natl Univ, Inst Environm Sci & Technol, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
[2] Japan Sci & Technol Corp, CREST, Kawaguchi 3320012, Japan
[3] Shimadzu Technores Inc, Nakagyo Ku, Kyoto 6048436, Japan
关键词
agrochemical; dioxin; dioxin-like PCB; impurity;
D O I
10.1016/S0045-6535(00)00310-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The profile and amount of dioxin impurity in agrochemicals were studied through detailed analysis of historic Japanese formulations. The chemicals analyzed include pentachlorophenol (PCP), 2,4,6-trichlorophenyl-4 ' -nitrophenyl ether (chloronitrofen, CNP), 2,4-dichlorophenyl-4 ' -nitrophenyl ether (nitrofen, NIP), tetrachloro-iso-phthalonitrile (chlorothalonil, TPN), 2-methyl-4-chloro-phenoxyacetic acid (MCP) and 2,4-dichlorophenoxyacetic acid (2,4-D), Among the six, two herbicides, PCP and CNP, produced during the 1960s and 1970s, contained very high concentrations of PCDD/DFs and TEQ. Others contained relatively low concentrations of PCDD/DFs. Dioxin-like PCB concentrations in all chemicals studied were low and their contributions to TEQ were negligible. The total dioxin emissions from the use of agrochemicals in Japan during the past 40 years (1955-1995) were estimated to be about a few hundred thousand kg of PCDD/DFs and 250 kg of WHO-TEQ from PCP and 190 x 10(3) kg of PCDD/DFs and 440 kg of WHO-TEQ from CNP. The major dioxin congeners present in PCP formulations were highly chlorinated PCDD/ DFs that can be formed by the coupling of PCP and/or 2,3,4,6-tetrachlorophenol, and those in the CNP formulations were tetra- to hexa-chlorinated PCDD/DFs that can be formed from 2,4,6-trichlorophenol and/or 2,3,4,6-tetrachlorophenol. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:873 / 885
页数:13
相关论文
共 12 条
[1]  
[Anonymous], 1979, ANN NY ACAD SCI, DOI 10.1111/j.1749-6632.1979.tb56588.x
[2]  
BUSER HR, 1976, J ASSOC OFF ANA CHEM, V59, P562
[3]   ISOMERSPECIFIC ANALYSIS OF PENTACHLOROPHENOL AND SODIUM PENTACHLOROPHENATE FOR 2,3,7,8-SUBSTITUTED PCDD AND PCDF AT SUB-PPB LEVELS [J].
HAGENMAIER, H ;
BRUNNER, H .
CHEMOSPHERE, 1987, 16 (8-9) :1759-1764
[4]  
HANAI Y, 1997, UNPUB
[5]  
MASUNAGA S, 1998, ORGANOHALOGEN COMPD, V39, P81
[6]  
MORITA M, 1991, CONCENTRATION DIOXIN, P96
[7]   IDENTIFICATION OF POLYCHLORINATED DIBENZOFURANS (PCDFS) IN COMMERCIAL CHLOROPHENOL FORMULATIONS [J].
RAPPE, C ;
GARA, A ;
BUSER, HR .
CHEMOSPHERE, 1978, 7 (12) :981-991
[8]   MECHANISMS OF FORMATION OF POLYCHLORINATED DIBENZO (PARA) DIOXINS (PCDDS) AND POLYCHLORINATED DIBENZOFURANS (PCDFS) FROM POTENTIAL INDUSTRIAL SOURCES [J].
REE, KCM ;
EVERS, EHG ;
VANDENBERG, M .
TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY, 1988, 17 (03) :171-195
[9]  
RYAN JJ, 1991, J CHROMATOGR, V541, P134
[10]  
SCHECTER A, 1997, ORGANOHALOGEN COMPOU, V32, P51