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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

Co-firing of biomass with coals Part 1. Thermogravimetric kinetic analysis of combustion of fir (abies bornmulleriana) wood

TL;DR: In this paper, the chemical composition and reactivity of fir (Abies bornmulleriana) wood under non-isothermal thermogravimetric (TG) conditions were studied.
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Non-isothermal melt-crystallization and mechanical properties of titanium(IV) oxide nanoparticle-filled isotactic polypropylene

TL;DR: In this paper, the effect of the addition of titanium(IV) oxide (TiO 2 ) with diverse surface characteristics (i.e., neat, silica (SiO 2 ),coated and stearic acid-coated) on non-isothermal melt-crystallization, subsequent melting behavior and mechanical properties of filled isotactic polypropylene (iPP) was investigated.
Journal ArticleDOI

High Speed SPM Applied for Direct Nanoscale Mapping of the Influence of Defects on Ferroelectric Switching Dynamics

TL;DR: In this article, a high speed variation of Scanning Probe Microscopy with continuous image rates on the order of 1 frame per second is applied to investigate the nucleation and growth of individual ferroelectric domains.
Journal ArticleDOI

Unified description of the rate of nucleation-mediated crystal growth

TL;DR: In this article, the steady-state rate of nucleation-mediated growth of crystals is described by a unified expression combining the known equations for mononuclear and polynuclear growth mechanisms.
Journal ArticleDOI

Large-scale production of alkali-resistant Shirasu porous glass (SPG) membranes: Influence of ZrO2 addition on crystallization and phase separation in Na2O–CaO–Al2O3–B2O3–SiO2 glasses; and alkali durability and pore morphology of the membranes

TL;DR: In this paper, a crystalline phase of wollastonite (CaSiO 3 ) was formed in the ZrO 2 -free mother glass heat-treated at approximately 900°C, corresponding to the glass-shaping temperature.
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''.