{"title":"Systematic Studies on the Breakdown of p,p'-DDT in Tobacco Smokes","authors":"N. M. Chopra, J. Domanski, N. B. Osborne","doi":"10.2478/cttr-2013-0231","DOIUrl":null,"url":null,"abstract":"Abstract These studies, on the pyrolysis of DDT, can be divided into two sections. Section 1 deals with the pyrolysis of p,p'-DDT in a nitrogen atmosphere at 900°C and subsequent isolation and identification of CH2Cl2, CHCl3, CCl4, CHCl = CCl2, CCl2 = CCl2, chlorobenzene, CCl3- CCl3, a,p-dichlorotoluene, p,p'-dichlorobiphenyl, bis-(p-chlorophenyl)methane, cis-p,p'-dichlorostilbene, bis-(p-chlorophenyI)chloromethane, p,p'-DDM, p,p'-DDE, trans-p,p'-dichlorostilbene, p,p'-TDE, and p,p'-DDT. Mechanisms for the formation of these compounds are proposed, and on that basis prediction is made on the formation of DDT degradation products when DDT-treated tobacco is smoked. Section 2 deals with pyrolytic degradation of DDT incorporated in tobacco. Methyl chloride, bis-(p-chlorophenyl)methane, p,p'-dichlorobenzophenone, p,p'-DDM, trans-p,p'-dichlorostilbene, p,p'-DDE, p,p'-TDE and p,p'-DDT were identified as the pyrolysis products. Based on the type and nature of pyrolysis products obtained, eight conclusions are made.","PeriodicalId":35431,"journal":{"name":"Beitrage zur Tabakforschung International/ Contributions to Tobacco Research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1970-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Beitrage zur Tabakforschung International/ Contributions to Tobacco Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2478/cttr-2013-0231","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 6
Abstract
Abstract These studies, on the pyrolysis of DDT, can be divided into two sections. Section 1 deals with the pyrolysis of p,p'-DDT in a nitrogen atmosphere at 900°C and subsequent isolation and identification of CH2Cl2, CHCl3, CCl4, CHCl = CCl2, CCl2 = CCl2, chlorobenzene, CCl3- CCl3, a,p-dichlorotoluene, p,p'-dichlorobiphenyl, bis-(p-chlorophenyl)methane, cis-p,p'-dichlorostilbene, bis-(p-chlorophenyI)chloromethane, p,p'-DDM, p,p'-DDE, trans-p,p'-dichlorostilbene, p,p'-TDE, and p,p'-DDT. Mechanisms for the formation of these compounds are proposed, and on that basis prediction is made on the formation of DDT degradation products when DDT-treated tobacco is smoked. Section 2 deals with pyrolytic degradation of DDT incorporated in tobacco. Methyl chloride, bis-(p-chlorophenyl)methane, p,p'-dichlorobenzophenone, p,p'-DDM, trans-p,p'-dichlorostilbene, p,p'-DDE, p,p'-TDE and p,p'-DDT were identified as the pyrolysis products. Based on the type and nature of pyrolysis products obtained, eight conclusions are made.