1975
DOI: 10.1002/chin.197517153
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ChemInform Abstract: PHOTODECOMPOSITION OF MIREX ON SILICA GEL CHROMATOPLATES EXPOSED TO NATURAL AND ARTIFICIAL LIGHT

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Cited by 6 publications
(10 citation statements)
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“…Any 5b-hydroCLD detected in the environment must then necessarily come from a man-made bishomocubane structure. It is known that 5b-hydroCLD may be formed by photoreaction with sunlight of the perchlorinated bishomocubane pesticides, Mirex (C 10 Cl 12 ) and CLD (Ivie et al 1974) and so also from a compound such as Kelevan that is a source of CLD upon breakdown of the bond connecting its CLD and levulinate moieties (Maier-Bode 1976). However, there is no evidence that Kelevan has ever been used in the FWI.…”
Section: Different Physical Behaviour Of 5b-hydrocld and Cld Resultinmentioning
confidence: 99%
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“…Any 5b-hydroCLD detected in the environment must then necessarily come from a man-made bishomocubane structure. It is known that 5b-hydroCLD may be formed by photoreaction with sunlight of the perchlorinated bishomocubane pesticides, Mirex (C 10 Cl 12 ) and CLD (Ivie et al 1974) and so also from a compound such as Kelevan that is a source of CLD upon breakdown of the bond connecting its CLD and levulinate moieties (Maier-Bode 1976). However, there is no evidence that Kelevan has ever been used in the FWI.…”
Section: Different Physical Behaviour Of 5b-hydrocld and Cld Resultinmentioning
confidence: 99%
“…As an example, in the USA, only 2.2 and 8.5 % of Mirex spreads in a field in 1962, at a concentration of 1 ppm, were recovered 12 years later in the soils of this field under the form of CLD and 5b-hydromirex, respectively (Carlson et al 1976), which are known precursors of 5b-hydroCLD under the action of light and UV Ivie et al 1974). The production of 5b-hydroCLD from these compounds occurs, however, with an extremely slow kinetics, even when sunlight exposure is optimum (Ivie et al 1974), which is obviously not the case of a compound buried in soil.…”
Section: Different Physical Behaviour Of 5b-hydrocld and Cld Resultinmentioning
confidence: 99%
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“…Photomirex is not a commercial product, but chlordecone was marketed as an insecticide until 1976, when severe health and environmental effects were identified at its production site in Hopewell, VA (16). Photomirex has been identified as a contaminant of fish in Lake Ontario, presumably as a result of mirex production at Niagara Falls, NY (1) and subsequent exposure of the mirex to UV light (17). In addition to their close chemical relationship, both mirex and chlordecone are highly lipophilic, highly persistent, and carcinogenic (3,(18)(19)(20).…”
Section: Introductionmentioning
confidence: 99%