期刊
ANALYTICAL CHEMISTRY
卷 88, 期 24, 页码 12066-12071出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.6b02597
关键词
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资金
- Natural Sciences and Engineering Research Council of Canada (NSERC)
- Canada Research Chair Program
- Chemours Canada Company
Volatilization causes changes in the isotopic composition of organic compounds as a result of different vapor pressures of molecules containing heavy and light isotopes. Both normal and inverse vapor pressure isotope effects (VPIE) have been observed, depending on molecular interactions in the liquid phase and the investigated element. Previous studies have focused mostly on pure compound volatilization or on compounds dissolved in organic liquids. Environmentally relevant scenarios, such as isotope fractionation during volatilization of organics from open water surfaces, have largely been neglected. In the current study, open-system volatilization experiments (focusing thereby on kinetic/-nonequilibrium effects) were carried out at ambient temperatures for trichloromethane, trichloroethene, trichlorofluoromethane, trichlorotrifluoroethane, methanol, and ethanol dissolved in water and, if not previously reported in the literature for these compounds, for volatilization from pure liquids. Stable carbon isotopic signatures were measured using continuous flow isotope ratio mass spectrometry. The results demonstrate that volatilization of the four halogenated compounds from water does not cause a measurable change in the carbon isotopic composition, whereas for pure-phase evaporation, significant inverse isotope effects are consistently observed (+0.3 parts per thousand< epsilon < + 1.7 parts per thousand). In contrast, methanol and ethanol showed normal isotope effects for evaporation of pure organic liquids (-3.9 parts per thousand and -1.9 parts per thousand) and for volatilization of compounds dissolved in water (-4.4 parts per thousand and -2.9 parts per thousand), respectively. This absence of measurable carbon isotope fractionation considerably facilitates the application of isotopic techniques for extraction of field samples and preconcentration of organohalogens-known to be important pollutants in groundwater and in the atmosphere.
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