Long-term sustainability of reductive dechlorination reactions at chlorinated solvents sites

被引:4
作者
Newell, CJ [1 ]
Aziz, CE [1 ]
机构
[1] Groundwater Serv Inc, Houston, TX 77098 USA
关键词
biodegradation; chlorinated solvents; electron acceptors; natural attenuation; reductive dechlorination; sustainability;
D O I
10.1023/B:BIOD.0000044682.92391.bb
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The sustainability of biodegradation reactions is of interest at Type I chlorinated solvent sites where monitored natural attenuation is being considered as a remedial alternative. Type I chlorinated solvent sites are sites undergoing reductive dechlorination where anthropogenic substrates (such as landfill leachate or fermentable organics in the waste materials) ferment to produce hydrogen, a key electron donor. A framework is provided that classifies Type I chlorinated solvent sites based on the relative amounts and the depletion rates of the electron donors and the electron acceptors (i.e., chlorinated solvents). Expressions are presented for estimating the total electron donor demand due to the presence of solvents and competing electron acceptors such as dissolved oxygen, nitrate, and sulfate. Finally, a database of 13 chlorinated solvent sites was analyzed to estimate the median and maximum mass discharge rate for dissolved oxygen, nitrate. and sulfate flowing into chlorinated solvent plumes. These values were then used to calculate the amount of hydrogen equivalents and potential for lost perchloroethylene (PCE) biodegradation represented by the inflow of these competing electron acceptors. The median and maximum mass of PCE biodegradation lost due to competing electron acceptors, assuming 100% efficiency, was 226 and 4621 kg year(-1), respectively.
引用
收藏
页码:387 / 394
页数:8
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