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Abstract¡G

The aim of this study is to investigate the influence of environmental factors, including pH value, temperature, chloride, and pitting inhibitor, on the corrosion fatigue properties of AISI 347 stainless steel.  In particular, the high-cycle fatigue (HCF) and fatigue crack growth (FCG) behavior in air and five aqueous environments were made a comparison.  The effect of environmentally assisted cracking mechanisms on the degradation of fatigue resistance was characterized.  The electrochemical properties in five aqueous environments were also made a comparison.  Fractography and microstructural analyses with optical microscopy (OM) and scanning electron microscopy (SEM) were conducted to determine the corrosion fatigue crack initiation and propagation modes.

Results showed that the fatigue strength of AISI 347 in H2SO4 and 3.5% NaCl solutions was lower than that in air, water, 80oC water, and 3.5% NaCl with inhibitor; especially fatigue strength in H2SO4 was the lowest.  However, the FCG rates in all environments were almost the same.  These results indicated that the initial fatigue cracking stage controlled the HCF life of AISI 347.

The H2SO4 and 3.5% NaCl solutions had more detrimental effects on the HCF of AISI 347 in crack initiation and stage I cracking stages as compared with other aqueous environments.  The fatigue-strength reduction in 3.5% NaCl solution resulted from the formation of corrosion pits as the stress concentrations for premature fatigue crack initiation.  The lower pH value in H2SO4 would dissolve the protective passive surface film and enhance the synergism between corrosive environment and cyclic stresses leading to the shorter fatigue life by reducing the periods of stage I cracking and transition from stage I to stage II cracking.  Adding pitting inhibitor in 3.5% NaCl solution can prevent formation of corrosion pits on specimen surface and extend HCF life.  This is due to the fact that the inhibitor added in 3.5% NaCl solution can prevent pitting formation by reacting with the metal ions to form a protective film on specimen surface.

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