Part VII – July 1969 - Papers - The Dissolution and Growth Kinetics of Spherical Precipitates

The American Institute of Mining, Metallurgical, and Petroleum Engineers
Frank V. Nolfi Paul G. Shewmon James S. Foster
Organization:
The American Institute of Mining, Metallurgical, and Petroleum Engineers
Pages:
7
File Size:
442 KB
Publication Date:
Jan 1, 1970

Abstract

Analytical expressions are developed for the kinetics of dissolution or growth of a spheroidized, solute rich stoichiometric Precipitate in the surrounding matrix. There are two limiting cases; in one the rate of dissolution or growth is limited by long range solute diffusion through the matrix and in the other by the transfer of atoms across the mrdrix-precipitate interface. In the former case local interfacial equilibrium exists while in the latter it does not and the rate of dissolution or growth is controlled by an interfacial reaction. The analysis treats both limiting cases as well as mixed control in a single development, where it is found that the thermodynamic state of the interface is completely specified by a single parameter, o, defined by where K is the reaction rate constant, D is the matrix solute diffusivity, and R, is the precipitate radiz~s. If K is infinite then a is zero and local equilibrium prevails; if K deviates infinitesimally from zero, then a is very near unity and an interfacial reaction is rate controlling. Mixed control occurs for intermediate values of o. From the analytical results, numbers are computed which are useful in determining the duration of interfacial reaction or mixed control; following this time period, long range diffusion is rate controlling. THE rate controlling process or processes governing phase boundary migration has been the subject of much speculation and investigation. Traditionally, the most widely assumed boundary condition in quantitative treatments of this problem has been that of local interfacial equilibrium. This condition implies that long range diffusion of one or more elements controls the migration and is referred to as "diffusion controlled migration" (herein DCM). In contrast to the above view is the proposition that local interfacial equilibrium does not exist and that transport of atoms across the interface is rate controlling. Consequently, this mechanism is referred to as "interface controlled migration" (herein ICM). In processes of the latter type, the activity, a, of one or more elements is discontinuous at the phase bound- ary and the flux, J, across the boundary of a given element is some function of its activity discontinuity, a. One of the most comprehensive contributions to a mathematical description of phase boundary migration is due to am.' His analyses are applicable to precipitation in binary systems in which a) the precipitates are spherical* solute rich compounds of constant
Citation

APA: Frank V. Nolfi Paul G. Shewmon James S. Foster  (1970)  Part VII – July 1969 - Papers - The Dissolution and Growth Kinetics of Spherical Precipitates

MLA: Frank V. Nolfi Paul G. Shewmon James S. Foster Part VII – July 1969 - Papers - The Dissolution and Growth Kinetics of Spherical Precipitates. The American Institute of Mining, Metallurgical, and Petroleum Engineers, 1970.

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