Transformation of Chlorofluorocarbons Investigated via Stable Carbon Compound-Specific Isotope Analysis
Author(s) -
Elizabeth Phillips,
Tetyana Gilevska,
Axel Horst,
Jesse Manna,
Edward S. Seger,
Edward J. Lutz,
Scott Norcross,
Scott A. Morgan,
Kathryn A. West,
E. Erin Mack,
Sandra Dworatzek,
Jennifer Webb,
Barbara Sherwood Lollar
Publication year - 2019
Publication title -
environmental science and technology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.851
H-Index - 397
eISSN - 1520-5851
pISSN - 0013-936X
DOI - 10.1021/acs.est.9b05746
Subject(s) - environmental chemistry , isotope analysis , chemistry , isotopes of carbon , biotransformation , groundwater , environmental remediation , fractionation , isotope fractionation , contamination , total organic carbon , chromatography , organic chemistry , geology , ecology , oceanography , geotechnical engineering , biology , enzyme
Compound-specific isotope analysis (CSIA) is a valuable tool in contaminant remediation studies. Chlorofluorocarbons (CFCs) are ozone-depleting substances previously thought to be persistent in groundwater under most geochemical conditions but more recently have been found to (bio)transform in some laboratory experiments. To date, limited applications of CSIA to CFCs have been undertaken. Here, biotransformation-associated carbon isotope enrichment factors, ε C,bulk for CFC-113 (ε C,bulk = -8.5 ± 0.4‰) and CFC-11 (ε C,bulk = -14.5 ± 1.9‰), were determined. δ 13 C signatures of pure-phase CFCs and hydrochlorofluorocarbons were measured to establish source signatures. These findings were applied to investigate potential in situ CFC transformation in groundwater at a field site, where carbon isotope fractionation of CFC-11 suggests naturally occurring biotransformation by indigenous microorganisms. The maximum extent of CFC-11 transformation is estimated to be up to 86% by an approximate calculation using the Rayleigh concept. CFC-113 δ 13 C values in contrast were not resolvably different from pure-phase sources measured to date, demonstrating that CSIA can aid in identifying which compounds may, or may not, be undergoing reactive processes at field sites. Science and public attention remains focused on CFCs, as unexplained source inputs to the atmosphere have been recently reported, and the potential for CFC biotransformation in surface and groundwaters remains unclear. This study proposes δ 13 C CSIA as a novel application to study the fate of CFCs in groundwater.
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