HYDROGEN ISOTOPE FRACTIONATION BETWEEN KAOLINITE AND WATER REVISITED

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dc.contributor.author Gilg H.A.
dc.contributor.author Sheppard S.M.F.
dc.date.accessioned 2020-11-23T10:53:31Z
dc.date.available 2020-11-23T10:53:31Z
dc.date.issued 1996
dc.identifier https://elibrary.ru/item.asp?id=491618
dc.identifier.citation Geochimica et Cosmochimica Acta, 1996, , 3, 529-533
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/19403
dc.description.abstract The equilibrium hydrogen isotope fractionation factor (α) between kaolinite and water in the temperature range 330 to 0°C is 1000 ln αkaol-water = ?2.2 ? 106 T?2 ? 7.7. This monotonic expression is based on a combination of experimental data with ?75% of exchange and empirical calibrations. The previously proposed and widely accepted complex fractionation expression is considered to reflect the role of surface and intersite fractionation effects in the low percent of exchange experiments (Liu and Epstein, 1984), and incorrect δD water values for the empirical values (Lambert and Epstein, 1980). There is no measurable fractionation between dickite and kaolinite. The temperature dependence of the kaolinite-water hydrogen isotope fractionation factor can probably be used as a model for other phyllosilicate-water systems below 350°C.
dc.title HYDROGEN ISOTOPE FRACTIONATION BETWEEN KAOLINITE AND WATER REVISITED
dc.type Статья


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