Diffusionless transformations, also referred to as displacive transformations, are solid-state changes in the crystal structure that do not rely on the diffusion of atoms over long distances. Instead, they occur due to coordinated shifts in atomic positions, where atoms move by a distance less than the span between neighboring atoms while maintaining their relative arrangement. An illustrative instance of this is the martensitic transformation observed in steel. The term "martensite" was initially used to designate the hard and finely dispersed constituent that forms in rapidly cooled steels. Subsequently, it was discovered that other materials, including non-ferrous alloys and ceramics, can undergo diffusionless transformations as well. As a result, the term "martensite" has taken on a more inclusive meaning to encompass the resulting product of such transformations. With diffusionless transformations, there is some form of cooperative, homogenous movement that results in a change to the crystal structure during a phase change. These movements are small, usually less than their interatomic distances, and the neighbors of an atom remain close. The systematic movement of large numbers of atoms led to some to refer to these as military transformations in contrast to civilian diffusion-based phase changes, initially by Frederick Charles Frank and John Wyrill Christian.
The most commonly encountered transformation of this type is the martensitic transformation which, while probably the most studied, is only one subset of non-diffusional transformations. The martensitic transformation in steel represents the most economically significant example of this category of phase transformations. However, an increasing number of alternatives, such as shape memory alloys, are becoming more important as well.
When a structural change occurs by the coordinated movement of atoms (or groups of atoms) relative to their neighbors, the change is termed a displacive transformation. This covers a broad range of transformations so further classifications have been developed.
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Diffusionless transformations, also referred to as displacive transformations, are solid-state changes in the crystal structure that do not rely on the diffusion of atoms over long distances. Instead, they occur due to coordinated shifts in atomic positions, where atoms move by a distance less than the span between neighboring atoms while maintaining their relative arrangement. An illustrative instance of this is the martensitic transformation observed in steel.
Austenite, also known as gamma-phase iron (γ-Fe), is a metallic, non-magnetic allotrope of iron or a solid solution of iron with an alloying element. In plain-carbon steel, austenite exists above the critical eutectoid temperature of 1000 K (727 °C); other alloys of steel have different eutectoid temperatures. The austenite allotrope is named after Sir William Chandler Roberts-Austen (1843–1902); it exists at room temperature in some stainless steels due to the presence of nickel stabilizing the austenite at lower temperatures.
Martensite is a very hard form of steel crystalline structure. It is named after German Adolf Martens. By analogy the term can also refer to any crystal structure that is formed by diffusionless transformation. Martensite is formed in carbon steels by the rapid cooling (quenching) of the austenite form of iron at such a high rate that carbon atoms do not have time to diffuse out of the crystal structure in large enough quantities to form cementite (Fe3C). Austenite is gamma-phase iron (γ-Fe), a solid solution of iron and alloying elements.
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The microstructure of many alloys and ceramics are constituted of very fine intricate domains (variants) created by diffusive or displacive phase transformations. The course introduces the crystallogr
The objective of this project is to analyse welding processes in high strength low-carbon steel grade S690 in numerical simulation with MORFEO codes and in experiments with a Gleeble® thermo-mechanica
Gamma titanium aluminide (γ-TiAl) based alloys are very interesting materials for structural applications at elevated temperatures owing to the combination of high specific strength, good oxidation, c
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