Abstract
The rate limiting mechanisms for reductive dechlorination of carbon tetrachloride (CT) and tetraethylene chloride (TCE) involve electron transfer were determined. The apparent Ea for CT reduction decreased with increasingly negative electrode potentials, suggesting that the rate of CT dechlorination is controlled by an electron transfer step. In contrast to CT, the Ea values for TCE exhibited a slight increase with decreasing E. Rates of CT reduction at iron surfaces were limited by the rate of electron transfer, while rates of TCE reduction were limited by chemical dependent factors. Reduction via an outer sphere mechanism might explain why halogenated alkanes undergo stepwise reductive dechlorination and produce chlorinated byproducts. In contrast, inner sphere reactions, which might involve chemisorption and thus produce longer interactions with the iron surface, might explain why the primary pathway for chlorinated alkene reduction produces few detectable chlorinated byproducts. This is an abstract of a paper presented at the 222nd ACS National Meeting (Chicago, IL 8/26-30/2001).
Original language | English (US) |
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Pages (from-to) | 739-744 |
Number of pages | 6 |
Journal | ACS Division of Environmental Chemistry, Preprints |
Volume | 41 |
Issue number | 2 |
State | Published - 2001 |
Event | 222nd ACS National Meeting - Chicago, IL, United States Duration: Aug 26 2001 → Aug 30 2001 |
ASJC Scopus subject areas
- General Chemical Engineering