Influence of chloride cations on pore solution chloride and critical chloride threshold of carbon steel rebar

Author(s):  
I.G. Ogunsanya ◽  
L. Kristufek ◽  
P. Le Meur ◽  
C.M. Hansson
CORROSION ◽  
2006 ◽  
Vol 62 (10) ◽  
pp. 892-904 ◽  
Author(s):  
M. F. Hurley ◽  
J. R. Scully

Abstract The threshold chloride concentration for solid Type 316LN (UNS S31653) stainless steel, Type 316L (UNS S31603) stainless steel clad, 2101 (UNS S32101), Fe-9%Cr, and carbon steel rebar (ordinary ASTM A 615M) was investigated using potentiodynamic and potentiostatic current monitoring techniques in saturated calcium hydroxide (Ca[OH]2) + sodium chloride (NaCl) solutions. There is general consensus in this study and the literature that the chloride threshold for carbon steel is less than a chloride to hydroxl (Cl−/OH−) molar ratio of 1. Solid Type 316LN stainless steel rebar was found to have a much higher chloride threshold (i.e., threshold Cl−/OH− ratio > 20) than carbon steel (0.25 < Cl−/OH−< 0.34). Type 316L stainless steel clad rebar possessed a chloride threshold expressed as a Cl−/OH− ratio of 4.9 when cladding was intact. However, surface preparation, test method, duration of period exposed to a passivating condition prior to the introduction of chloride, and the presence of cladding defects all affected the threshold chloride concentration obtained. For instance, the presence of mill scale on any of the more corrosion-resistant materials reduced the chloride threshold to approximately that of carbon steel. The chloride threshold for Type 316L clad rebar was highly dependent on any defects that exposed the carbon steel core. At best, it was similar to that of solid stainless steel. However, when defective, it was equal to that of carbon steel rebar in the potentiostatic method used here. A model was implemented to predict the extension of the Cl− diffusion time period until corrosion initiation would be expected using rebar materials with a higher chloride threshold concentration than carbon steel. Model results confirmed that corrosion-resistant rebar materials in a pickled condition may increase time until chloride-induced breakdown of passivity and onset of corrosion to 100 years or more.


CORROSION ◽  
2012 ◽  
Vol 68 (4) ◽  
pp. 045003-1-045003-10 ◽  
Author(s):  
M. Akhoondan ◽  
A.A. Sagüés

The extent of the oxygen reduction reaction in concrete was evaluated for ~9% Cr rebar approaching the ASTM A1035 specification and compared to that of conventional carbon steel rebar, at ages of up to ~1 year. Cathodic strength was measured by the cathodic current density developed at −0.35 V vs. copper/copper sulfate (Cu/CuSO4 [CSE]) and −0.40 VCSE in cyclic cathodic potentiodynamic polarization tests, both in the as-received condition with mill scale and with scale removed by glass bead surface blasting. In both conditions the ~9% Cr alloy was a substantially weaker cathode, by a factor of several fold, than carbon steel. Within each material, the surface-blasted condition yielded also much lower cathodic current density than the as-received condition. For a small anode-large cathode system with a given anode polarization function, and no important oxygen reduction concentration polarization, the corrosion current was projected to be significantly lower if the cathodic region were ~9% Cr instead of plain steel rebar with comparable surface condition. There was strong correlation between the charge storage capability of the interface and the extent of cathodic reaction of oxygen. The result cannot be ascribed solely to differences in effective surface area between the different materials and conditions.


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