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Unidirectional transformation of Fe-0.8C-Co alloys: Part II. Kinetics of the eutectoid reaction

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TLDR
In this article, unidirectional transformation was applied to a study of the kinetics of eutectoid growth in Fe-0.8C-Co alloys.
Abstract
Unidirectional transformation techniques have been applied to a study of the kinetics of eutectoid growth in Fe-0.8C-Co alloys. The technique readily yielded kinetic data which it is shown could be used to indicate the rate controlling process for pearlitic growth. Accurate measurements of interlamellar spacing (λ) could be made at controlled growth rates (V) and analyzed in terms of the expressionVλn, where the exponentn can indicate the rate controlling process. The results obtained by unidirectional transformation were compared with those achieved by conventional isothermal transformation, both to aid in the initial interpretation of the more unfamiliarV:λ data and also to show that the two different experimental routes lead to equivalent kinetic data. Analysis of the results obtained for Fe-0.8C-Co alloys suggested control by interfacial diffusion of carbon at high growth rates (n=3) changing towards volume diffusion of carbon at lower growth rates (n=2), but also revealed an unexpected region at very slow growth rates (n=4). This anomalous region could be explained in terms of the partitioning of cobalt as the growth rate decreased. It was also shown that cobalt additions decreased the pearlite interlamellar spacing at constant undercooling or growth rate.

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Citations
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Journal ArticleDOI

A Review of the Data on the Interlamellar Spacing of Pearlite

TL;DR: In this article, the relationship between interlamellar spacing and temperature for isothermal growth conditions and between translation velocity and spacing for forced-velocity growth conditions is reviewed for a range of steels and nonferrous alloys.
Journal ArticleDOI

Unidirectional transformation of Fe-0.8C-Co alloys: Part I. Process per structure relationships and the significance of pearlite interlamellar spacing measurements

TL;DR: In this paper, a comparison between the temperature gradient calculated to maintain a single planar interface by preventing nucleation ahead of the interface and that actually required in the experiment led to the conclusion that the temperature gradients must retard the nucleation of pearlite.
Journal ArticleDOI

Pearlite in Multicomponent Steels: Phenomenological Steady-State Modeling

TL;DR: In this article, a steady-state model for austenite-to-pearlite transformation in multicomponent steel is presented, including Fe, C, and eight more elements, and a smooth and physical transition between orthopearlite and parapearlite is realized by optimizing the partitioning of substitutional alloying elements between ferrite and cementite to maximize growth rate or dissipation rate.
Journal ArticleDOI

Partitioning of Co during pearlite growth in a eutectoid steel

N. Ridley, +1 more
- 01 Jan 1984 - 
TL;DR: Partitioning of cobalt between ferrite and cementite during the isothermal decomposition of austenite to pearlite has been studied for a 2.1 wt%Co eutectoid steel using analytical electron microscopy of two stage extraction replicas as mentioned in this paper.
References
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Constitution of Binary Alloys

Max Hansen, +1 more
Journal ArticleDOI

The pearlite reaction

TL;DR: In this article, a critical appraisal of theory and experiments for both isothermal and forced velocity pearlite is presented, and a new perturbation procedure for definition of the optimal steady-state spacing is presented.
Journal ArticleDOI

The free energy of formation and the interfacial enthalpy in pearlite

TL;DR: In this article, a constant heat-flow calorimeter was used to measure the enthalpy of the pearlite-austenite transformation as a function of pearlite spacing in the iron-carbon and copper-aluminum eutectoids.
Journal ArticleDOI

The edgewise growth of pearlite

TL;DR: In this article, the edgewise growth rate of pearlite into austenite has been computed on the assumptions that interface diffusion is the dominant means of carbon transport and that local equilibrium exists across all interfaces.
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