Martensite

For the transformation, see Diffusionless transformations.

Iron alloy phases
Ferrite (α-iron, δ-iron) Austenite (γ-iron) Pearlite (88% ferrite, 12% cementite) Martensite Bainite Ledeburite (austenite-cementite eutectic, 4.3% carbon) Cementite (iron carbide, Fe3C) Beta ferrite (β-iron) Hexaferrum (ε-iron)
Steel classes
Crucible steel Carbon steel (≤2.1% carbon; low alloy) Spring steel (low or no alloy) Alloy steel (contains non-carbon elements) Maraging steel (contains nickel) Stainless steel (contains ≥10.5% chromium) Weathering steel Tool steel (alloy steel for tools)
Other iron-based materials
Cast iron (>2.1% carbon) Ductile iron Gray iron Malleable iron White iron Wrought iron (contains slag)
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Martensite in AISI 4140 steel

0.35%C Steel, water-quenched from 870°C

Martensite, named after the German metallurgist Adolf Martens (1850–1914), most commonly refers to a very hard form of steel crystalline structure, but it can also refer to any crystal structure that is formed by displacive transformation.^[1] It includes a class of hard minerals occurring as lath- or plate-shaped crystal grains. When viewed in cross-section, the lenticular (lens-shaped) crystal grains appear acicular (needle-shaped), which is how they are sometimes incorrectly described.^[vague]

In the 1890s, Martens studied samples of different steels under a microscope, and found that the hardest steels had a regular crystalline structure.^[1] He was the first to explain the cause of the widely differing mechanical properties of steels. Martensitic structures have since been found in many other practical materials, including shape memory alloys and transformation-toughened ceramics.^[1]

The martensite is formed by rapid cooling (quenching) of austenite which traps carbon atoms that do not have time to diffuse out of the crystal structure. This martensitic reaction begins during cooling when the austenite reaches the martensite start temperature (M_s) and the parent austenite becomes mechanically unstable. At a constant temperature below M_s, a fraction of the parent austenite transforms rapidly, then no further transformation will occur.^[1] When the temperature is decreased, more of the austenite transforms to martensite. Finally, when the martensite finish temperature (M_f) is reached, the transformation is complete. Martensite can also be formed by application of stress (this property is frequently used in toughened ceramics like yttria-stabilized zirconia and in special steels like TRIP steels (i.e. transformation induced plasticity steels)). Thus, Martensite can be thermally induced or stress induced.^[1]

One of the differences between the two phases is that martensite has a body-centered tetragonal (BCT) crystal structure, whereas austenite has a face-centered cubic (FCC) structure. The transition between these two structures requires very little thermal activation energy because it is a martensitic transformation, which results in the subtle but rapid rearrangement of atomic positions, and has been known to occur even at cryogenic temperatures.^[1] Martensite has a lower density than austenite, so that the martensitic transformation results in a relative change of volume.^[2] Of considerably greater importance than the volume change is the shear strain which has a magnitude of about 0.26 and which determines the shape of the plates of martensite.^[3]

Martensite is not shown in the equilibrium phase diagram of the iron-carbon system because it is not an equilibrium phase. Equilibrium phases form by slow cooling rates allowing sufficient time for diffusion, whereas martensite is usually formed by fast cooling rates. Since chemical processes (the attainment of equilibrium) accelerate at higher temperature, martensite is easily destroyed by the application of heat. This process is called tempering. In some alloys, the effect is reduced by adding elements such as tungsten that interfere with cementite nucleation, but, more often than not, the phenomenon is exploited instead. Since quenching can be difficult to control, many steels are quenched to produce an overabundance of martensite, then tempered to gradually reduce its concentration until the right structure for the intended application is achieved. Too much martensite leaves steel brittle, too little leaves it soft.

See also

• Eutectoid
• Ferrite (iron)
• Maraging steel
• Spring steel
• Tool steel

References

1. ^ ^{a b c d e f} Khan, Abdul Qadeer (March 1972) [1972], "3" (in German and English), The effect of morphology on the strength of copper-based martensites,, 1, 1 (1 ed.), Leuven, Belgium: A.Q. Khan, University of Leuven, Belgium, pp. 300 
2. ^ Ashby, Michael F.; & David R. H. Jones (1992) [1986]. Engineering Materials 2 (with corrections ed.). Oxford: Pergamon Press. ISBN 0-08-032532-7. 
3. ^ Bhadeshia, H. K. D. H. (2001) [2001]. Geometry of Crystals (with corrections ed.). London: Institute of Materials. ISBN ISBN 0-904357-94-5. 

External links

• Comprehensive resources on martensite, from the University of Cambridge