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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

X-ray diffraction study of the hydrogen reduction of NiO/α-Al2O3 steam reforming catalysts

TL;DR: In this paper, the authors measured NiO disappearance and Ni appearance simultaneously, together with the crystallite size of each, using in situ hot-stage X-ray diffraction in the temperature range 175-900°C.
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Recrystallization behavior of a high-manganese steel: Experiments and simulations

TL;DR: In this article, the thermal treatment of a 30% cold-rolled Fe-28Mn-0.28C twinning-induced plasticity (TWIP) steel was investigated.
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Quantification of phase transformation kinetics of 18 wt.% Ni C250 maraging steel

TL;DR: In this paper, the phase transformation kinetics of an 18 ¾wt.% Ni maraging grade C250 was investigated using differential scanning calorimetry (DSC).
Journal ArticleDOI

Phase field modeling of void nucleation and growth in irradiated metals

TL;DR: In this paper, a phase field model for void formation in metals with vacancy concentrations exceeding the thermal equilibrium values is presented, which allows for a unified treatment of void nucleation and growth under the condition of random generation of vacancies, which is similar to vacancy generation by collision cascade in irradiated materials.
Journal ArticleDOI

Novel synthesis of Ni/Fe layered double hydroxides using urea and glycerol and their enhanced adsorption behavior for Cr(VI) removal

TL;DR: It is suggested that the modified Ni/Fe LDH/GL materials were promising nanoadsorbents for efficient potassium dichromate removal and chemical stability and recyclability of these adsorbents were studied.
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''.