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Title: Abiotic dehalogenation of 1,2-dichloroethane and 1,2-dibromoethane in aqueous solution containing hydrogen sulfide

Technical Report ·
OSTI ID:6728838

The detection of significant levels of halogenated aliphatic contaminants in groundwater resources in the United States has spurred a considerable effort to understand the various mechanisms--both microbiological and abiotic--by which these compounds may be transformed. In aerobic environments, the abiotic reactions that predominate are elimination of hydrogen halide (dehydrohalogenation) and nucleophilic substitution by H{sub 2}O (hydrolysis). Little research has examined the rates and pathways of abiotic reactions that may be significant under hypoxic conditions. The dehalogenation of 1,2-dichloroethane (1,2-DCA) and 1,2-dibromoethane (EDB) in phosphate buffer was examined alone, and in phosphate buffer containing hydrogen sulfide. Kinetic runs were conducted at pH 7 over the temperature range from 25 to 87.5 C. Phosphate buffer catalyzed the hydrolysis of both 1,2-SCA and EDB. This catalysis was attributed to the buffer anion HPO4(2-). The rate laws for these transformations exhibit the following form: -d(RX)/dt=(K{sup 1}{sub H}) + K{sub HS{minus}}(HS{sup {minus}}) + K{sub HPO4(2-)}(HPO4(2-))(RX) where RX denotes either 1,2-DCA or EDB, and the rate constants correspond to the overall reactions.

Research Organization:
Stanford Univ., CA (USA). Dept. of Civil Engineering
OSTI ID:
6728838
Report Number(s):
PB-90-216284/XAB
Resource Relation:
Other Information: Pub. in Environmental Science and Technology, Vol. 23, No. 11, 1349-1358(Nov 1989)
Country of Publication:
United States
Language:
English