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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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Influence of Additions of Anatase TiO2 Nanoparticles on Early-Age Properties of Cement-Based Materials

TL;DR: In this paper, the effect of chemically nonreactive anatase TiO2 nanoparticles on early-age hydration of portland cements was investigated through isothermal calorimetry and measurements of chemical shrinkage.
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Isothermal crystallization kinetics and crystal structure of poly(lactic acid): Effect of triphenyl phosphate and talc

TL;DR: In this article, the results showed that the average value of Avrami exponents n is around 2.0 for neat poly(lactic acid) (PLA) and its blends with triphenyl phosphate (TPP) and/or talc crystallized isothermally in the temperature range of 113-128°C.
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Palm oil hydrolysis by lipase from Candida cylindracea immobilized on zeolite type Y

TL;DR: In this paper, the lipase was used to hydrolyze palm oil in a microaqueous two-phase reaction system containing isooctane as organic medium and lecithin as surfactant.
Journal ArticleDOI

Effects of the degree of undercooling on flow induced crystallization in polymer melts

TL;DR: In this paper, the authors investigated the coupled effects of mild shear flow and temperature on the crystallization behavior of two thermoplastic polymers, namely, an isotactic polypropylene and an isotactically poly(1-butene).
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Structural and thermal stability criteria of Bi2O3–B2O3 glasses

TL;DR: In this paper, the authors used IR spectroscopy to estimate the glass thermal stability in the above composition range and added the kinetic parameter Kr(T) to the stability criteria.
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''.