Abstract

The effects of hydrogen on crack growth in martensitic AISI 4340 steel are shown to be fundamentally the same whether the hydrogen is supplied as molecular gas, through stress corrosion, or by electrolytic charging. At a given yield strength differences observed in the values of threshold stress intensity for crack growth are proposed to be linked to the degree of dissociation of the hydrogen near the crack tip, and hence to the concentration of hydrogen developed in the critical crack-tip region. Over a range of yield strength values, an upper bound of threshold stress intensity is developed in molecular hydrogen gas and a lower bound on exposure to atomic hydrogen from cathodic charging during or prior to testing. The open circuitK Iscc values of the steel fall always within the upper and lower bounds, but the values ofK Iscc may be moved to the lower bound by coupling to magnesium (cathodic charging) or to the upper bound by coupling to copper (anodic polarization). Variations in the concentration of carbon or manganese in the steel at a fixed yield strength produce effects on the value ofK Iscc similar to the effects produced by cathodic or anodic polarization. With the lower concentrations of carbon or manganese the steel acts as if it were coupled to copper and at the higher concentrations as if coupled to magnesium. Carbon and manganese are therefore proposed to shift the positions of local anodes and cathodes and so influence the proportions of molecular and atomic hydrogen which reach the critical crack-tip region. The proposal is supported by data which show that only cathodic polarization affects the threshold stress intensity of the lowest carbon and manganese steelsK Iscc is lowered) whereas only anodic polarization affects the higher carbon or manganese steels(K Iscc is raised).

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