Assessment of anaerobic biodegradation of bis(2-chloroethyl) ether in groundwater using carbon and chlorine compound-specific isotope analysis

被引:3
作者
Segal, Daniel C. [1 ]
Kuder, Tomasz [3 ]
Kolhatkar, Ravi [2 ]
机构
[1] Chevron Energy Technol Co, San Ramon, CA 94583 USA
[2] Chevron Energy Technol Co, Houston, TX 77002 USA
[3] Univ Oklahoma, Sch Geol & Geophys, Norman, OK 73019 USA
关键词
CSIA; Dual-element isotope analysis; Groundwater; Bis(2-chloroethyl) ether; BCEE; Anaerobic biodegradation; RATIO MASS-SPECTROMETRY; REDUCTIVE DEHALOGENATION; MICROBIAL-DEGRADATION; HYDROGEN-SULFIDE; FRACTIONATION; 1,2-DICHLOROETHANE; TRICHLOROETHENE; PATHWAYS; FIELD; 1,2-DIBROMOETHANE;
D O I
10.1016/j.scitotenv.2017.12.246
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Carbon and chlorine compound specific isotope analysis (CSIA) of bis(2-chloroethyl) ether (BCEE) was performed to distinguish the primary processes contributing to observed concentration reductions in an anaerobic groundwater plume. Laboratory microcosms were constructed to demonstrate and obtain isotopic enrichment factors and dual-element CSIA trends from two potential transformation processes (1) anaerobic biodegradation using saturated sediment samples fromthe field site (epsilon(C) = -14.8 and epsilon(Cl) = -5.0) and (2) abiotic reactions with sulfide nucleophiles in water (epsilon(C) = -12.8 and epsilon(Cl) = -5.0). The results suggested a nucleophilic, SN2-type dechlorination as the mechanism of biodegradation of BCEE. Identical dual-element CSIA trends observed in the field and in the microcosm samples suggested that the same degradation mechanism was responsible for BCEE degradation in the field. While biodegradation was the likely dominant mechanism of BCEE mass destruction in the aquifer, potential contribution of abiotic hydrolysis to the net budget of degradation could not be confidently excluded. To our knowledge, this is the first unequivocal demonstration of BCEE biodegradation at a field site. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:696 / 705
页数:10
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