Proceedings of the International rilem conference Materials, Systems and Structures in Civil Engineering 2016



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98

International RILEM Conference on Materials, Systems and Structures in Civil Engineering 

Conference segment on Service Life of Cement-Based Materials and Structures 

22-24 August 2016, Technical University of Denmark, Lyngby, Denmark 

 

 

Figure 3. Electrochemical setup 



2.4

 

Observation of corrosion products, of steel/concrete interface and estimation of the 

crack patterns  

 

Visual observations 

After the accelerated corrosion test, the specimens were observed and a special focus was 

made on the top and the front sides because of their lower concrete cover (30mm). Cracks 

opening were measured with a crack measuring magnifier (resolution 0.1mm) on these two 

surfaces. Then the specimens were sliced (125x100x20mm

3

), considering corroded areas as 



illustrated in [Figure 4]. After 24h drying in an oven at 45°C, the slices were photographied 

and examined in order to characterize the crack pattern (angle and length) [Figure 5]. To 

determine the angular position, the methodology developed by Sanz-Merino [8] was adopted 

[Figure 5-a]. To estimate the length of the cracks in each cross-sections, the photographs of 

the cross-section and a circle graduated every centimeter were superimposed as shown in 

[Figure 5-b]. Moreover, the corrosion products embedding the rebar and filling the concrete 

cracks were analyzed. Then from both results an attempt was made to correlate what was seen 

on the concrete surface in 2Dimensions (by the bridge's owner) and what happened inside the 

concrete with an aim of 3Dimensions. 

 

Scanning Electron Microscopy observations 

The slices were then impregnated with an epoxy resin under vaccum (to prevent decohesion 

between concrete and steel when the corrosion damage was severe) and then cut into samples 

which dimensions (2x4.5x4.5cm

3

) fitted in the Scanning Electron Microscopy  (SEM) 



observation room. A first goal is to determine the corrosion product thickness and their length 

circling the perimeter of the rebar. A second objective is to observe the crack pattern and the 

transfer of the oxides through the cracks.  

 

 




99

International RILEM Conference on Materials, Systems and Structures in Civil Engineering 

Conference segment on Service Life of Cement-Based Materials and Structures 

22-24 August 2016, Technical University of Denmark, Lyngby, Denmark 

 

 

 



Figure 4. Specimen sawing design (25 slices named Tn° according to the axis. Corrosion test 

zone is between x=10 and x= 40 cm 



 

 

 

Figure 5. Determination of the crack angular position (a) and the crack length (b) after the 



accelerated corrosion test on the two sections of a slice  



PVC tank length = 27.5 cm 

T10 


T13 

T16 


(a) 

(b) 



100

International RILEM Conference on Materials, Systems and Structures in Civil Engineering 

Conference segment on Service Life of Cement-Based Materials and Structures 

22-24 August 2016, Technical University of Denmark, Lyngby, Denmark 

 

3.

 

Experimental results 

3.1

 

Voltage evolution during the accelerated corrosion test

 

Figure 6. Voltage evolution during the accelerated corrosion test 



[Figure 6] shows the voltage evolution for each RC specimen subjected to the accelerated 

corrosion test versus time. Before the test (time=0), the voltage reflects the electrical 

resistance of the specimens which are in a close range from 2.5 to 3 V except for P004-7d 

specimen (3.3V). During the test, three stages are observed. In the first stage, the voltage 

increase (about 1V) may be explained by the formation of resistive iron oxides (passive layer) 

[9], [10] around the rebar and also by the diffusion into the concrete and the filling up of the 

concrete pores by the oxides in the vicinity of the steel. In the second step, the drastic voltage 

decrease (50% loss) can arise from the concrete cracking and the steel / concrete debonding. 

The last stage with a constant voltage (1.4V) appears for longer durations, 28d and 35d and is 

likely representative of a constant impedance of the corrosion layer. These preliminary 

observations need to be discussed considering the migration of the ionic species under current 

and particularly the penetration of the chloride ions. Tests are under progress.  



3.2

 

Corrosion rate and crack patterns 

[Figure 7] shows the corrosion signs and the cracks observed for the top side and the front 

side of the two specimens after an accelerated corrosion test of 21 days.  

Regarding the top sides, specimen P-007 shows some corrosion product stains and a visible 

crack roughly along the steel rebar whereas specimen P-008 is not damaged. Regarding the 

front sides, the opposite behaviour is observed: specimen P-007 only exhibits a single spot of 

corrosion product while specimen P-008 shows significant corrosion products along the crack 



101

International RILEM Conference on Materials, Systems and Structures in Civil Engineering 

Conference segment on Service Life of Cement-Based Materials and Structures 

22-24 August 2016, Technical University of Denmark, Lyngby, Denmark 

 

that follows the rebar. An assumption to explain this difference could be that the aggregate as 



well as the rebar's ribs are not homogeneously distributed and promote this heterogeneity.  

 

Top side P-007-21d 



Top side P-008-21d 

 

Front side P-007-21d 



Front side P-008-21d 

Figure 7. Qualitative results of the specimens after an accelerated corrosion of 21 days 

 

[Figure 8] reveals that all corroded specimens for over 14 days have a J



corr

 equal to 10 μA/cm² 

approximately except the specimen P-004-7d corroded for 7 days. The proposed assumption 

is that at 7 days chloride ions have not reached the steel/concrete interface yet and 

consequently, the corrosion is still passive. To give an answer to this question, chloride 

measurement ingress with AgNO

3

 will be achieved on each slice. Regarding the crack width



the behaviour of corroded specimens is different. As previously mentioned, all specimens are 

not cracked on the same side. As already suggested, this difference could be ascribed to the 

heterogeneity of the concrete (the random distribution of the aggregates into the cement 

paste). Besides, the crack on the top side is wider than the one on the front side. This 

observation might be attributed to the close localization of the counter electrode on the top 

side of the specimen (by comparison with the steel rebar) that permits chloride ions to quickly 

reach the rebar (modification of the physico-chemical conditions that locally enhances the 

corrosion process).  

[Figure 9] shows the evaluation of the crack patterns (angular position (a), length (b) and 

width (c)) for each of the 10 cross-sections of the five slices of specimen P-008-21d. The 

cracks propagate from the steel/concrete interface to the concrete surface.  

 



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