Most approaches that have been proposed for the remediation of groundwater contaminated with CCl 4 produce chloroform as the major product and methylene chloride as a minor product. Both of these products are nearly as persistent and problematic as the parent compound, but competing reaction pathways produce the more desirable products CO and/or formate. To improve the applicability of reductive remediation technologies to the large plumes of CCl 4 at several DOE sites, the complete characterization of the mechanisms and kinetics of competing degradation reactions of CCl 4 were studied through laboratory experiments closely coordinated with theoretical modeling studies. The results are starting to suggest strategies for maximizing the yield of desirable products from CCl 4 degradation, which will be tested in column model systems using real site waters and matrix materials. This is an abstract of a paper presented at the 227th ACS National Meeting (Anaheim, CA 3/28/2004-4/1/2004).
|Original language||English (US)|
|Journal||ACS National Meeting Book of Abstracts|
|State||Published - Jun 1 2004|
|Event||227th ACS National Meeting Abstracts of Papers - Anaheim, CA., United States|
Duration: Mar 28 2004 → Apr 1 2004
ASJC Scopus subject areas
- Chemical Engineering(all)