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Journal ArticleDOI

Granulation, Phase Change, and Microstructure Kinetics of Phase Change. III

Melvin Avrami
- 01 Feb 1941 - 
- Vol. 9, Iss: 2, pp 177-184
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TLDR
In this paper, a comprehensive description of the phenomena of phase change may be summarized in Phase Change, Grain Number and Microstructure Formulas or Diagrams, giving, respectively, the transformed volume, grain, and microstructure densities as a function of time, temperature, and other variables.
Abstract
The theory of the preceding papers is generalized and the notation simplified. A cluster of molecules in a stable phase surrounded by an unstable phase is itself unstable until a critical size is reached, though for statistical reasons a distribution of such clusters may exist. Beyond the critical size, the cluster tends to grow steadily. The designation ``nuclei'' or ``grains'' is used according as the clusters are below or above the critical size. It is shown that a comprehensive description of the phenomena of phase change may be summarized in Phase Change, Grain Number and Microstructure Formulas or Diagrams, giving, respectively, the transformed volume, grain, and microstructure densities as a function of time, temperature, and other variables. To facilitate the deduction of formulas for these densities the related densities of the ``extended'' grain population are introduced. The extended population is that system of interpenetrating volumes that would obtain if the grains granulated and grew through each other without mutual interference. The extended densities are much more readily derivable from an analysis of the fundamental processes of granulation and growth. It is shown that, under very general circumstances, the densities of the actual grain population may be expressed simply in terms of the extended population.

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Citations
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Journal ArticleDOI

A three-dimensional microstructural model of reactions and transport in aqueous mineral systems

TL;DR: In this paper, a stochastic three-dimensional microstructure model is introduced for simulating spatial and temporal variations in aqueous mineral systems, where dissolution, nucleation, precipitation and solute transport are governed by local probabilistic rules applied on a regular computational lattice.
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Electrocrystallization: Nucleation and growth of nano-clusters on solid surfaces

TL;DR: Theoretical and experimental findings related to the stationary and non-stationary nucleation kinetics, growth of single two-and three-dimensional crystals as well as underpotential deposition phenomena and spatial distribution of clusters are reviewed and referred to suitable sources of reliable information on the most important subjects concerned as mentioned in this paper.
Journal ArticleDOI

Electrical, Mechanical, and Structural Characterization of Self-Assembly in Poly(3-hexylthiophene) Organogel Networks

TL;DR: In this paper, the authors investigate the potential to design an interconnected network of conjugated polymers using the gelation of poly(3-hexylthiophene) (P3HT) as a model system.
Journal ArticleDOI

The use of the JMAYK kinetic equation for the analysis of solid-state reactions: critical considerations and recent interpretations

TL;DR: In this article, the classical Johnson-Mehl-Avrami-Yerofeev-Kolmogorov (JMAYK) equation is used for recrystallization of plastically deformed metals.
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Strain Effect on the γ′ Dissolution at High Temperatures of a Nickel-Based Single Crystal Superalloy

TL;DR: In this article, a modified Polystar model is proposed to incorporate the role of the accumulated plastic strain on the γ′ dissolution kinetics and to achieve a better predictability of the creep deformation under non-isothermal loading paths.
References
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Journal ArticleDOI

Kinetics of Phase Change. I General Theory

TL;DR: In this paper, the theory of phase change is developed with the experimentally supported assumptions that the new phase is nucleated by germ nuclei which already exist in the old phase, and whose number can be altered by previous treatment.
Journal ArticleDOI

Kinetics of Phase Change. II Transformation‐Time Relations for Random Distribution of Nuclei

TL;DR: In this article, a relation between the actual transformed volume V and a related extended volume V1 ex is derived upon statistical considerations, and a rough approximation to this relation is shown to lead, under the proper conditions, to the empirical formula of Austin and Rickett.
Journal ArticleDOI

Grand Partition Functions and So‐Called ``Thermodynamic Probability''

TL;DR: The relation due to Boltzmann between entropy and thermodynamic probability is enunciated in a precise form in this paper and generalized in such a way that each of the other thermodynamic potentials is related in a similar manner to a ''thermodynamic probability'' for which a more suitable name is a ''partition function''.