Use of carbon stable isotope to investigate chloromethane formation in the electrolytic dechlorination of trichloroethylene [An article from: Journal of Hazardous Materials] Buy on Amazon

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Use of carbon stable isotope to investigate chloromethane formation in the electrolytic dechlorination of trichloroethylene [An article from: Journal of Hazardous Materials]

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Book Details

PublisherElsevier
ISBN / ASINB000PDTYOK
ISBN-13978B000PDTYO2
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States  🇺🇸

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This digital document is a journal article from Journal of Hazardous Materials, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Carbon stable isotope trichloroethylene (^1^3C TCE) was used to investigate the formation of chloromethane (CM) during the electrolytic dechlorination of trichloroethylene (TCE) at a granular-graphite packed cathode. A method was developed to use a conventional GC/MS to analyze and quantify regular and ^1^3C TCE and their dechlorination products. The concentration of a ^1^3C compound can be calculated, based on the concentration of its regular counterpart, from the response ratio of two fragments of different mass per charge values from the compounds in a sample and two characteristic MS spectrum ratios: one is the response ratio of the two fragments of the regular compound, and the other is the response ratio of the corresponding fragments of the regular and ^1^3C compounds at the same concentrations. The method was used to analyze the regular and ^1^3C compounds observed in an experiment of dechlorination in an ammonium acetate solution that contained both regular TCE and ^1^3C TCE. Results of analysis confirmed that CM was not a direct product of TCE dechlorination at the granular graphite cathode that cis-DCE was an intermediate product of TCE dechlorination, and that 1,1-DCE was not a dechlorination product.
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