TY - JOUR
T1 - Hydrogen Isotope Fractionation in the Epidote-Hydrogen and Epidote-Water Systems
T2 - Theoretical Study and Implications
AU - Asaduzzaman, Abu
AU - Ganguly, Jibamitra
N1 - Funding Information:
This research was supported by National Aeronautics and Space Administration (NASA) Grant NNX14AG28G. Thanks are due to the anonymous reviewers and Merlin Meh́ eut for their critical comments and raising some important questions. Revision of the manuscript and providing additional details in the Supporting Information file in response to these questions has led to significant improvement of the manuscript. The authors are grateful to Prof. Sumit Chakraborty for his judicious and insightful editorial handling and making specific suggestions to make the methodological aspects more convincing and Drs. Donato Belmonte, Krishna Muralidharan, and Tom Chacko for helpful discussions.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/10/18
Y1 - 2018/10/18
N2 - Experimental data for hydrogen isotope and, in general, stable isotope fractionation between mineral and water often tend to be widely divergent primarily because of solution and reprecipitation of finely ground mineral grains in the experimental charges. With the objective of development of a theoretical methodology for calculation of stable isotope fractionation that may be suitably integrated with experimental data to produce better constraints on the fractionation behavior, we have calculated hydrogen isotope fractionation in the epidote-water and epidote-hydrogen systems, for which reliable experimental data are available. The calculations were carried out using a combination of classical and statistical thermodynamics and quantum chemical methods. The calculated fractionation factors versus temperature in both systems have been found to be in very good agreement with the experimental data and provide a theoretical framework for extrapolation of experimental data as a function of temperature.
AB - Experimental data for hydrogen isotope and, in general, stable isotope fractionation between mineral and water often tend to be widely divergent primarily because of solution and reprecipitation of finely ground mineral grains in the experimental charges. With the objective of development of a theoretical methodology for calculation of stable isotope fractionation that may be suitably integrated with experimental data to produce better constraints on the fractionation behavior, we have calculated hydrogen isotope fractionation in the epidote-water and epidote-hydrogen systems, for which reliable experimental data are available. The calculations were carried out using a combination of classical and statistical thermodynamics and quantum chemical methods. The calculated fractionation factors versus temperature in both systems have been found to be in very good agreement with the experimental data and provide a theoretical framework for extrapolation of experimental data as a function of temperature.
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U2 - 10.1021/acsearthspacechem.8b00076
DO - 10.1021/acsearthspacechem.8b00076
M3 - Article
AN - SCOPUS:85053941505
SN - 2472-3452
VL - 2
SP - 1029
EP - 1034
JO - ACS Earth and Space Chemistry
JF - ACS Earth and Space Chemistry
IS - 10
ER -