Monitoring trichloroethene remediation at an iron permeable reactive barrier using stable carbon isotopic analysis

被引:39
作者
VanStone, N
Przepiora, A
Vogan, J
Lacrampe-Couloume, G
Powers, B
Perez, E
Mabury, S
Lollar, BS
机构
[1] Univ Toronto, Stable Isotope Lab, Toronto, ON M5S 3B1, Canada
[2] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
[3] EnviroMet Technol Inc, Waterloo, ON N2V 2G6, Canada
[4] URS Corp, Denver, CO 80237 USA
[5] AFCEE, ERD FEW, FE Warren AFB, WY 82005 USA
基金
加拿大自然科学与工程研究理事会;
关键词
carbon isotopes; groundwater remediation; permeable reactive barrier; reductive dechlorination; trichloroethene; zero-valent iron;
D O I
10.1016/j.jconhyd.2005.05.013
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Stable carbon isotopic analysis, in combination with compositional analysis, was used to evaluate the performance of an iron permeable reactive barrier (PRB) for the rernediation of ground water contaminated with trichloroethene (TCE) at Spill Site 7 (SS7), F.E. Warren Air Force Base, Wyoming. Compositional data indicated that although the PRB appeared to be reducing TCE to concentrations below treatment goals within and immediately downgradient of the PRB, concentrations remained higher than expected at wells further downgradient (i.e. > 9 m) of the PRB. At two wells downgradient of the PRB, TCE concentrations were comparable to upgradient values, and delta C-13 values of TCE at these wells were not significantly different than upgradient values. Since the process of sorption/desorption. does not significantly fractionate carbon isotope values, this suggests that the TCE observed at these wells is desorbing from local aquifer materials and was present before the PRB was installed. In contrast, three other downgradient wells show significantly more enriched delta C-13 values compared to the upgradient mean. In addition, delta C-13 values for the degradation products of TCE, cis-dichloroethene and vinyl chloride, show fractionation patterns expected for the products of the reductive dechlorination of TCE. Since concentrations of both TCE and degradation products drop to below detection limit in wells within the PRB and directly below it, these downgradient chlorinated hydrocarbon concentrations are attributed to desorption from local aquifer material. The carbon isotope values indicate that this dissolved contaminant is subject to local degradation, likely due to in situ microbial activity. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:313 / 325
页数:13
相关论文
共 43 条
[1]  
AGRANOVICH MS, 1996, FUNKTSIONAL ANAL PRI, V30, P1
[2]   Kinetics of nitrate, nitrite, and Cr(VI) reduction by iron metal [J].
Alowitz, MJ ;
Scherer, MM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (03) :299-306
[3]   Dechlorination of carbon tetrachloride by Fe(II) associated with goethite [J].
Amonette, JE ;
Workman, DJ ;
Kennedy, DW ;
Fruchter, JS ;
Gorby, YA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (21) :4606-4613
[4]  
[Anonymous], 1999, NATURAL ATTENUATION
[5]   Isotopic characterization of chlorinated solvents-laboratory and field results [J].
Beneteau, KM ;
Aravena, R ;
Frape, SK .
ORGANIC GEOCHEMISTRY, 1999, 30 (8A) :739-753
[6]   Carbon isotope fractionation during abiotic reductive dehalogenation of trichloroethene (TCE) [J].
Bill, M ;
Schüth, C ;
Barth, JAC ;
Kalin, RM .
CHEMOSPHERE, 2001, 44 (05) :1281-1286
[7]   Carbon isotope fractionation during microbial dechlorination of trichloroethene, cis-1,2-dichloroethene, and vinyl chloride:: Implications for assessment of natural attenuation [J].
Bloom, Y ;
Aravena, R ;
Hunkeler, D ;
Edwards, E ;
Frape, SK .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (13) :2768-2772
[8]  
Clark I., 1997, ENV ISOTOPES HYDROLO, DOI DOI 10.1201/9781482242911
[9]   Carbon isotopic fractionation during reductive dehalogenation of chlorinated ethenes by metallic iron [J].
Dayan, H ;
Abrajano, T ;
Sturchio, NC ;
Winsor, L .
ORGANIC GEOCHEMISTRY, 1999, 30 (8A) :755-763
[10]   Tracing organic contaminants in groundwater: A new methodology using compound-specific isotopic analysis [J].
Dempster, HS ;
Lollar, BS ;
Feenstra, S .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (11) :3193-3197