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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. When the temperature is decreased, more of the austenite transforms to martensite. Finally, when the martensite finish temperature (Mf) is reached, the transformation is complete. Martensite can also form by application of stress (this property is frequently used in toughened ceramics like yttria stabilised zirconia and in special steels like TRIP steels (i.e. transformation induced plasticity steels). Thus, Martensite can be thermally induced or stress induced. 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.
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.
Category:Metallurgy Category:Metals Category:Ceramics Category:Steel
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