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Chloride-induced corrosion in steel-reinforced concrete under wet-dry conditions: Corrosion mechanism and critical chloride content
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Chloride-induced corrosion of steel is a major durability issue for reinforced concrete (RC) structures. The critical chloride content (
C
crit
), a key parameter in engineering, is generally studied under simplified exposure conditions. However, data on how wet-dry cycles – common in practice – affect
C
crit
and the corrosion mechanism are lacking. Thus, in this study, RC specimens were subjected to permanent immersion, daily wet-dry cycles (6/18 hours), and weekly cycles (2/5 days). Mass transport was studied by chloride profiling and moisture sorption tests, corrosion initiation was determined electrochemically, and corrosion products were identified by Raman spectroscopy. Cyclic exposure accelerated moisture and chloride ingress relative to immersion, reducing
C
crit
testing from 2–5 years to
∼
1 year.
C
crit
scattered widely in all exposure regimes (0.5
…
3.5% chloride by cement weight), and statistics showed at most weak inter-regime differences in
C
crit
. Post-autopsy Raman consistently identified chloride green rust near anodic zones and Fe(III) oxyhydroxides further away. Combined with thermodynamic modelling, these observations are consistent with established chloride-assisted pathways that can sustain localised corrosion under the exposure regimes tested. Finally, implications for
C
crit
laboratory testing are discussed.
Title: Chloride-induced corrosion in steel-reinforced concrete under wet-dry conditions: Corrosion mechanism and critical chloride content
Description:
Chloride-induced corrosion of steel is a major durability issue for reinforced concrete (RC) structures.
The critical chloride content (
C
crit
), a key parameter in engineering, is generally studied under simplified exposure conditions.
However, data on how wet-dry cycles – common in practice – affect
C
crit
and the corrosion mechanism are lacking.
Thus, in this study, RC specimens were subjected to permanent immersion, daily wet-dry cycles (6/18 hours), and weekly cycles (2/5 days).
Mass transport was studied by chloride profiling and moisture sorption tests, corrosion initiation was determined electrochemically, and corrosion products were identified by Raman spectroscopy.
Cyclic exposure accelerated moisture and chloride ingress relative to immersion, reducing
C
crit
testing from 2–5 years to
∼
1 year.
C
crit
scattered widely in all exposure regimes (0.
5
…
3.
5% chloride by cement weight), and statistics showed at most weak inter-regime differences in
C
crit
.
Post-autopsy Raman consistently identified chloride green rust near anodic zones and Fe(III) oxyhydroxides further away.
Combined with thermodynamic modelling, these observations are consistent with established chloride-assisted pathways that can sustain localised corrosion under the exposure regimes tested.
Finally, implications for
C
crit
laboratory testing are discussed.
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