TY - JOUR
T1 - Carbon and hydrogen isotopic fractionation of low molecular weight organic compounds during ultraviolet degradation
AU - Oba, Yasuhiro
AU - Naraoka, Hiroshi
N1 - Funding Information:
Professor R.E. Summons is acknowledged for bringing about this special issue based on the John M. Hayes Symposium held at the 16th V.M. Goldschmidt Conference. We also thank for two anonymous reviewers for their helpful comments to improve our manuscript. The work was supported by a research fellowship from the Japan Society for the Promotion of Science for Young Scientists (Y.O.) and a Grant-in-Aid for Scientific Research from the Japanese Ministry of Education, Science, Culture and Technology (H.N.).
PY - 2008/5
Y1 - 2008/5
N2 - Ultraviolet (UV) radiation is a ubiquitous energy source for chemical reactions in nature. In particular, UV radiation provides an important pathway for degradation of organic compounds. Although isotopic change in organic compounds exposed to UV radiation may be an indicator for evaluating the extent of degradation, the isotope behavior has not been yet clarified. In this study, stable carbon and hydrogen isotope fractionations were determined for volatile organic compounds including methanol, acetonitrile, benzene and propionic acid during UV degradation in order to reveal the isotopic behavior with respect to different functional groups. All the studied compounds became enriched in 13C and D with increase in UV exposure time. The isotopic fractionation factor (α) ranged from 0.9968 to 0.9875 for carbon, and from 0.9890 to 0.9406 for hydrogen. The order of carbon isotopic fractionation was different from that of hydrogen isotopic fractionation, probably due to intra- and inter-molecular reactions with different functional groups. UV degradation is a process potentially able to induce isotope enrichment in organic compounds in natural environments.
AB - Ultraviolet (UV) radiation is a ubiquitous energy source for chemical reactions in nature. In particular, UV radiation provides an important pathway for degradation of organic compounds. Although isotopic change in organic compounds exposed to UV radiation may be an indicator for evaluating the extent of degradation, the isotope behavior has not been yet clarified. In this study, stable carbon and hydrogen isotope fractionations were determined for volatile organic compounds including methanol, acetonitrile, benzene and propionic acid during UV degradation in order to reveal the isotopic behavior with respect to different functional groups. All the studied compounds became enriched in 13C and D with increase in UV exposure time. The isotopic fractionation factor (α) ranged from 0.9968 to 0.9875 for carbon, and from 0.9890 to 0.9406 for hydrogen. The order of carbon isotopic fractionation was different from that of hydrogen isotopic fractionation, probably due to intra- and inter-molecular reactions with different functional groups. UV degradation is a process potentially able to induce isotope enrichment in organic compounds in natural environments.
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U2 - 10.1016/j.orggeochem.2007.11.009
DO - 10.1016/j.orggeochem.2007.11.009
M3 - Article
AN - SCOPUS:42749090190
SN - 0146-6380
VL - 39
SP - 501
EP - 509
JO - Organic Geochemistry
JF - Organic Geochemistry
IS - 5
ER -