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The theory of transformations in metals and alloys

TL;DR: In this paper, the authors present a general introduction to the theory of transformation kinetics of real metals, including the formation and evolution of martensitic transformations, as well as a theory of dislocations.
Abstract: Part I General introduction. Formal geometry of crystal lattices. The theory of reaction rates. The thermodynamics of irreversable processes. The structure of real metals. Solids solutions. The theory of dislocations. Polycrystalline aggregates. Diffusion in the solid state. The classical theory of nucleation. Theory of thermally activated growth. Formal theory of transformation kinetics. Part II Growth from the vapour phase. Solidification and melting. Polymorphic Changes. Precipitation from supersaturated solid solution. Eutectoidal transformations. Order-disorder transformations. Recovery recrystalisation and grain growth. Deformation twinning. Characteristics of martensic transformations. Crystallography of martensitic transformations. Kinetics of martensitic transformations. Rapid solidification. Bainite steels. Shape memory alloys.
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Journal ArticleDOI
B.C. Shang1, Zhi Min Yin1, Guangrong Wang1, Bowei Liu1, Huang Zhucheng1 
TL;DR: In this paper, the quench sensitivity of 6082 aluminum alloy was investigated by time-temperature-property (TTP) curves and the important coefficients k 2 − k 5 and critical cooling rate for 6082 Al-alloy were identified, and the properties after different rates of cooling were predicted using quench factor analysis.

69 citations

Journal ArticleDOI
01 Nov 1971-Polymer
TL;DR: In this article, new theories of the crystallography of deformation twinning and phase transformations have been used to examine in detail for the first time the crystallographic processes which have been reported to occur in crystalline polyethylene.

69 citations

Journal ArticleDOI
TL;DR: In this article, a time integration scheme is presented for the martensitic phase transformation model developed in recent theoretical work of Turteltaub and Suiker (A multi-scale thermomechanical model for cubic to tetragonal martENSITIC phase transformations 2005; Transformation-induced plasticity in ferrous alloys 2005).
Abstract: SUMMARY A time integration scheme is presented for the martensitic phase transformation model developed in recent theoretical work of Turteltaub and Suiker (A multi-scale thermomechanical model for cubic to tetragonal martensitic phase transformations 2005; Transformation-induced plasticity in ferrous alloys 2005). The phase transformation model can be used for analysing transformation-induced plasticity (TRIP) phenomena in ferrous alloys. The microstructural information for the phase transformation model is provided by the crystallographic theory of martensitic transformations. The transformation characteristics depend on the specific transformation systems activated during a loading process. The time integration scheme is formulated within a framework of finite deformations, where the stressupdate algorithm is based on a fully implicit Euler backward discretization. A robust search algorithm is used for detecting the transformation systems activated during loading. The completion of the transformation process is prescribed by a constraint on the total martensitic volume fraction, which is accurately satisfied in the converged state using a sub-stepping algorithm. The computation of the consistent tangent operator is performed through a numerical differentiation method, which avoids the determination of extensive analytical derivatives and allows the model to be easily adapted if necessary. The ability of the algorithm to solve complex transformation-induced plasticity problems is illustrated with the aid of three-dimensional analyses, in which an aggregate of single-crystal grains of retained austenite embedded in a ferrite-based matrix is subjected to uniaxial tension. The response characteristics are in agreement with experimental findings of Jacques et al. (Philos. Mag. 2001; 81(7):1789; Metall. Mater. Trans. A 2001; 32A:2759) and Oliver et al. (Appl. Phys. A 2002; 74:S1143). Copyright 2005 John Wiley & Sons, Ltd.

69 citations

Journal ArticleDOI
TL;DR: This work presents a rigorous thermodynamic formulation of Fletcher's model using a novel analytical approach and discusses the new perspectives derived.
Abstract: Fletcher’s spherical substrate model [J. Chem. Phys. 29, 572 (1958)] is a basic model for understanding the heterogeneous nucleation phenomena in nature. However, a rigorous thermodynamic formulation of the model has been missing due to the significant complexities involved. This has not only left the classical model deficient but also likely obscured its other important features, which would otherwise have helped to better understand and control heterogeneous nucleation on spherical substrates. This work presents a rigorous thermodynamic formulation of Fletcher’s model using a novel analytical approach and discusses the new perspectives derived. In particular, it is shown that the use of an intermediate variable, a selected geometrical angle or pseudocontact angle between the embryo and spherical substrate, revealed extraordinary similarities between the first derivatives of the free energy change with respect to embryo radius for nucleation on spherical and flat substrates. Enlightened by the discovery, it was found that there exists a local maximum in the difference between the equivalent contact angles for nucleation on spherical and flat substrates due to the existence of a local maximum in the difference between the shape factors for nucleation on spherical and flat substrate surfaces. This helps to understand the complexity of the heterogeneous nucleation phenomena in a practical system. Also, it was found that the unfavorable size effect occurs primarily when R<5r∗ (R: radius of substrate and r∗: critical embryo radius) and diminishes rapidly with increasing value of R/r∗ beyond R/r∗=5. This finding provides a baseline for controlling the size effects in heterogeneous nucleation.

69 citations

Journal ArticleDOI
TL;DR: The nucleation of martensite is studied in defect-free single crystals of iron and iron-nickel over a size range of 0.002-0.2 µm as discussed by the authors.

68 citations