Inhibition, of Stress Corrosion Cracking of AISI 4340 Steel in 10% Potassium Nitrate Solution at 100 C

CORROSION ◽  
1972 ◽  
Vol 28 (10) ◽  
pp. 385-387
Author(s):  
H. R. BAKER ◽  
C. R. SINGLETERRY
CORROSION ◽  
1969 ◽  
Vol 25 (8) ◽  
pp. 342-344 ◽  
Author(s):  
A. TIRMAN ◽  
E. G. HANEY ◽  
PAUL FUGASSI

Abstract The resistance to stress corrosion cracking of AISI 4340 steel foil in 0.6M aqueous sodium chloride, acidified to pH 1.5 with hydrochloric acid, is greatly decreased by prior treatment of the specimens for short periods of time with aqueous and nonaqueous solutions of sulfur, organic and inorganic sulfides, sulfur dioxides, and the inorganic salts of sulfurousand sulfuric acids. It is suggested that this prior treatment produces sulfided areas which are inhibitors of the combination of atomic hydrogen into molecular hydrogen. The decreased resistance to stress corrosion cracking is thus attributed to hydrogen embrittlement. If the stress corrosion cracking test is made in 0.6M aqueous sodium chloride, adjusted to an initial pH of 8, the effect of a prior sulfiding treatment is small. The formation of such sulfided areas in practice result from the exposure of 4340 steels to industrial atmospheres which may contain hydrogen sulfide, sulfur dioxide, and elemental sulfur.


CORROSION ◽  
1972 ◽  
Vol 28 (9) ◽  
pp. 340-344 ◽  
Author(s):  
H. R. BAKER ◽  
C. R. SINGLETERRY

Abstract The effects of solutions of 16 different electrolytes on the stress corrosion cracking (SCC) of AISI 4340 steel U-bend specimens have been studied at various concentrations and at 25, 65, and 100 C (77, 149, and 212 F). Stresses were near the yield point of the alloy. In unbuffered solutions of neutral salts, there was poor correlation between time to failure and the initial or final pH of the solution. In strongly buffered solutions, there was a strong pH dependence; the time to failure in 10% NaCl increased about 100 fold between pH 4–5 and pH 7. Susceptibility to cracking increased moderately with the concentration of KNO3 solutions, but decreased with rising concentration of NaCl solutions. The cracking rate increased by 50% per 10 C for NaCl solutions. The rate increased 85% per 10 C for KNO3 solutions. KNO2 or NaNO2, dicyclohexylammonium nitrate, some K2CrO4 solutions and all alkaline solutions with a strong reserve of base inhibited SCC by factors of 10 to 100 times as compared with cracking in distilled H2O.


An important contributory role of grain boundary segregation of residual impurities in the intergranular stress-corrosion cracking of carbon and low alloy steels is proposed. Experimental results are presented of the stress corrosion susceptibility of mild steel in nitrate solution, and in relation to varying grain boundary composition as monitored by Auger electron spectroscopy. The harmfulness of a particular impurity element depends on three factors: its bulk level; its segregation thermodynamics and kinetics resulting in an equilibrium enrichment at the grain boundaries; and its ability to promote electrochemical dissolution of the grain boundary. A hierarchy of impurity elements that exacerbate stress corrosion cracking is presented and correlated with equilibrium oxidation potentials. The results and simple model allow the prediction of the relative harmfulness of impurity elements with respect to intergranular stress corrosion in commercial carbon and low alloy steels from a knowledge of the bulk concentration only. This enables significant improvements in performance to be designed in the alloy by respecifying lower levels of only the one or two highly detrimental impurities.


Sign in / Sign up

Export Citation Format

Share Document