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1 GeoKinetics, P.O. Box 1042, Lemont, Pennsylvania 16851, U.S.A.
2 Department of Earth Science MS-126, Rice University, 6100 Main Street, Houston, Texas 77251-1892, U.S.A.
Correspondence: * E-mail: aluttge{at}rice.edu
We introduce a general kinetic model for crystal dissolution that explicitly tracks all the various atoms in the crystal structure as part of the reaction mechanism. This model will be used in this and subsequent articles to develop a theory for the treatment of experimental and field water-rock kinetic data. The model is based on a many-body reaction mechanism. It is built from both elementary reactions, i.e., bond-breaking and bond-forming, and basic reactions, i.e., dissolution of surface units, adsorption and incorporation of solution units, and mobility of units at the crystal surface. The full crystal structure is used to calculate the interactions of neighboring atoms as well as possible defects of the crystal lattice in the model. This approach is different from models based on either molecular precursor complexes or adsorption.
We analyze several fundamental concepts such as activation energy, surface free energy, the solubility product, inhibition/catalysis, and saturation-state dependence using our approach. In addition, surface features such as nucleation, steps, and defects are presented and put in a quantitative basis in this paper. The resulting kinetic framework can handle explicitly any crystal structure, treating the actual bonding and position of all atoms within a given surface orientation in the structure. Investigation of the properties of such a general kinetic model leads to new relations between the activation energy and the net energy changes in the hydrolyses reactions, between surface free energy and activation energies and between inhibition and the statistical mechanics of kink sites. The kinetic model can actually account for the emergence of a solubility product from a reaction mechanism involving independent kinetics for the different species using steady-state concepts on the behavior of surface sites. The possible 
G dependence of the overall rate is studied with the general approach. Isotachs are used to exhibit the interplay of G and inhibition within a simple AB mineral structure. The crystal-based reaction mechanism not only leads to a unified explanation of many observed water-rock features but also produce a series of modifications of kinetic results not fully understood before.
This article has been cited by other articles:
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  L. Zhang and A. Luttge Al,Si order in albite and its effect on albite dissolution processes: A Monte Carlo study American Mineralogist, August 1, 2007; 92(8-9): 1316 - 1324. [Abstract] [Full Text] [PDF]
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A. Luttge Etch pit coalescence, surface area, and overall mineral dissolution rates American Mineralogist, November 1, 2005; 90(11-12): 1776 - 1783. [Abstract] [Full Text] [PDF]
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 A. Luttge, L. Zhang, and K. H. Nealson Mineral surfaces and their implications for microbial attachment: Results from Monte Carlo simulations and direct surface observations Am J Sci, June 1, 2005; 305(6-8): 766 - 790. [Abstract] [Full Text] [PDF]
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M. D. Vinson and A. Luttge Multiple length-scale kinetics: an integrated study of calcite dissolution rates and strontium inhibition Am J Sci, February 1, 2005; 305(2): 119 - 146. [Abstract] [Full Text] [PDF]
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