%0 Journal Article
%9 ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES
%A Pinilla, C.
%A Blanchard, M.
%A Balan, Etienne
%A Ferlat, G.
%A Vuilleumier, R.
%A Mauri, F.
%T Equilibrium fractionation of H and O isotopes in water from path integral molecular dynamics
%D 2014
%L fdi:010062034
%G ENG
%J Geochimica et Cosmochimica Acta
%@ 0016-7037
%M ISI:000335656900010
%P 203-216
%R 10.1016/j.gca.2014.03.027
%U https://www.documentation.ird.fr/hor/fdi:010062034
%> https://www.documentation.ird.fr/intranet/publi/2014/06/010062034.pdf
%V 135
%W Horizon (IRD)
%X The equilibrium fractionation factor between two phases is of importance for the understanding of many planetary and environmental processes. Although thermodynamic equilibrium can be achieved between minerals at high temperature, many natural processes involve reactions between liquids or aqueous solutions and solids. For crystals, the fractionation factor a can be theoretically determined using a statistical thermodynamic approach based on the vibrational properties of the phases. These calculations are mostly performed in the harmonic approximation, using empirical or ab-initio force fields. In the case of aperiodic and dynamic systems such as liquids or solutions, similar calculations can be done using finite-size molecular clusters or snapshots obtained from molecular dynamics (MD) runs. It is however difficult to assess the effect of these approximate models on the isotopic fractionation properties. In this work we present a systematic study of the calculation of the D/H and O-18/O-16 equilibrium fractionation factors in water for the liquid/vapour and ice/vapour phases using several levels of theory within the simulations. Namely, we use a thermodynamic integration approach based on Path Integral MD calculations (PIMD) and an empirical potential model of water. Compared with standard MD, PIMD takes into account quantum effects in the thermodynamic modeling of systems and the exact fractionation factor for a given potential can be obtained. We compare these exact results with those of modeling strategies usually used, which involve the mapping of the quantum system on its harmonic counterpart. The results show the importance of including configurational disorder for the estimation of isotope fractionation in liquid phases. In addition, the convergence of the fractionation factor as a function of parameters such as the size of the simulated system and multiple isotope substitution is analyzed, showing that isotope fractionation is essentially a local effect in the investigated system.
%$ 062 ; 064 ; 020