Lec 8 Super Alloys Intro

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    SUPERALLOYSINTRODUCTION & APPLICATIONS

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    Characteristics of high temperature materials

    First characteristic is an ability to withstandloading at an operating temperature close to

    its melting point.

    Homologous temperature

    this should be greater than about 0.6.

    Thus, a superalloy operating at 1000C in the

    vicinity of the melting temperature of nickel,1455C, working at a of (1000 + 273)/(1455 +

    273) 0.75, is classied as a high-temperature

    material.

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    A second characteristic is a substantial resistance to mechanical degradation over

    extended periods of time.

    For high-temperature applications, a time-dependent,inelastic and irrecoverable deformation known as creep mustbe considered due to the promotion of thermally activatedprocesses at high .

    Thus, as time increases, creep strain (creep) is accumulated;

    A nal characteristic is tolerance of severe operatingenvironments. For example, the hot gases generated in a coal-red

    electricity-generating turbine are highly corrosive due to thehigh sulphur levels in the charge.

    Kerosene used for aero engine fuel tends to be cleaner, butcorrosion due to impurities such as potassium salts and theingestion of sea-water can occur during operation.

    In these cases, the high operating temperatures enhance thepossibility of oxidation.

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    Turbine entry temperature (TET) is the temperature of the hot gases

    entering the turbine arrangement

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    The selection of materials for high-temperature applications

    Materials for high-temperature service must

    withstand considerable loads for extended

    periods of time.

    What are the best materials to choose for these

    applications? Can we justify the use of the superalloys which

    have nickel as the major constituent?

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    LarsonMiller approach for the ranking of creep performance

    Resistance to creep deformation is a major

    consideration. For many materials and under loading conditions

    which are invariant with time, the creep strainrate, ss , is constant; i.e. it approaches a steady-

    state.

    This implies a balance of

    creep hardening, for example, due to dislocationmultiplication and interaction with obstacles, and

    creep softening, for example, due to dislocationannihilation and recovery.

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    Very often, it is found that

    where is the applied stress,

    n is the stress exponent,

    A is a constant and Q is an activation energy.

    When a value for Q is deduced from the experimental creepdata, one often nds that it correlates with the activationenergy for self-diffusion. This implies that some form of masstransport on the scale of the microstructure is rate-controlling.

    Design against creep usually necessitates a consideration of

    the time to rupture, tr, which usually satises the so-calledMonkmanGrant relationship

    where B is a constant which is numerically equal to the creep ductility,i.e. the creep strain to failure.

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    At constant , one has

    where C and D are constants.

    The above Equation can be written in the form

    where P is known as the LarsonMiller parameterand Eisthe LarsonMiller constant;

    this is found to vary between 15 and 25 log h and is takento be 20 log h.

    When creep tests for various combinations of (, T) arecarried out, one usually nds a strong correlation betweenPand log , consistent with the assumptions made. Theseplots are known as LarsonMiller diagrams.

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    Nickel as a high-temperature material

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