Carbon and Hydrogen Isotope Fractionation of Benzene, Toluene, and o‐Xylene during Chemical Oxidation by Persulfate

Experiments were performed to investigate the carbon and hydrogen isotope fractionation of benzene, toluene, and o‐xylene (BTX) during chemical oxidation by unactivated persulfate at two concentrations (8 and 20 g/L). Carbon enrichment (ϵC) values of −1.7 ± 0.1‰ for benzene, −0.64 ± 0.1‰ for toluene...

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Veröffentlicht in:Ground water monitoring & remediation 2018-11, Vol.38 (4), p.62-72
Hauptverfasser: Solano, Felipe M., Marchesi, Massimo, Thomson, Neil R., Bouchard, Daniel, Aravena, Ramon
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container_issue 4
container_start_page 62
container_title Ground water monitoring & remediation
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creator Solano, Felipe M.
Marchesi, Massimo
Thomson, Neil R.
Bouchard, Daniel
Aravena, Ramon
description Experiments were performed to investigate the carbon and hydrogen isotope fractionation of benzene, toluene, and o‐xylene (BTX) during chemical oxidation by unactivated persulfate at two concentrations (8 and 20 g/L). Carbon enrichment (ϵC) values of −1.7 ± 0.1‰ for benzene, −0.64 ± 0.1‰ for toluene and −0.36 ± 0.04‰ for o‐xylene were obtained. No significant hydrogen enrichment (ϵH) was observed for benzene, while the hydrogen enrichment for toluene and o‐xylene were −20 ± 3‰ and −23 ± 2‰, respectively. The dual isotope plot (Δδ13C vs. Δδ2H) for benzene and o‐xylene revealed a distinct fractionation trend compared to the majority of the biodegradation data compiled from the literature; however, no unique trend was observed for toluene. The significant carbon and/or hydrogen enrichment, and the distinct trend observed on the dual isotope plot suggest that compound specific isotope analysis (CSIA) can potentially be used to monitor the chemical oxidation of BTX by persulfate, and to distinguish treatment areas where persulfate or biodegradation reactions are occurring for benzene and o‐xylene. Article Impact Statement: Carbon and hydrogen isotope fractionation of benzene, toluene and o‐xylene in the presence of persulfate established.
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Carbon enrichment (ϵC) values of −1.7 ± 0.1‰ for benzene, −0.64 ± 0.1‰ for toluene and −0.36 ± 0.04‰ for o‐xylene were obtained. No significant hydrogen enrichment (ϵH) was observed for benzene, while the hydrogen enrichment for toluene and o‐xylene were −20 ± 3‰ and −23 ± 2‰, respectively. The dual isotope plot (Δδ13C vs. Δδ2H) for benzene and o‐xylene revealed a distinct fractionation trend compared to the majority of the biodegradation data compiled from the literature; however, no unique trend was observed for toluene. The significant carbon and/or hydrogen enrichment, and the distinct trend observed on the dual isotope plot suggest that compound specific isotope analysis (CSIA) can potentially be used to monitor the chemical oxidation of BTX by persulfate, and to distinguish treatment areas where persulfate or biodegradation reactions are occurring for benzene and o‐xylene. 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subjects Benzene
Biodegradation
Carbon
Enrichment
Fractionation
Hydrocarbons
Hydrogen
Hydrogen enrichment
Hydrogen isotopes
Isotope fractionation
Isotopes
Organic chemistry
Oxidation
Toluene
Xylene
title Carbon and Hydrogen Isotope Fractionation of Benzene, Toluene, and o‐Xylene during Chemical Oxidation by Persulfate
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