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Application of electrochemical methods for studying steel corrosion in alkali-activated materials
(2023)
Alkali-activated materials (AAMs) are binders that can complement and partially substitute the current use of conventional cement. However, the present knowledge about how AAMs protect steel reinforcement in concrete elements is incomplete, and uncertainties exist regarding the application of electrochemical methods to investigate this issue. The present review by EFC WP11-Task Force ‘Corrosion of steel in alkali-activated materials’ demonstrates that important differences exist between AAMs and Portland cement, and between different classes of AAMs, which are mainly caused by differing pore solution compositions, and which affect the outcomes of electrochemical measurements. The high sulfide concentrations in blast furnace slag-based AAMs lead to distinct anodic polarisation curves, unusually low open circuit potentials, and low polarisation resistances, which might be incorrectly interpreted as indicating active corrosion of steel reinforcement. No systematic study of the influence of the steel–concrete interface on the susceptibility of steel to corrosion in AAMs is available. Less common electrochemical methods present an opportunity for future progress in the field.
Corrosion of steel rebars in concrete presents one of the main deterioration mechanisms limiting service life of the reinforced structures. The corrosion is accompanied by an expansion of the corrosion products causing high pressures, concrete cracking and finally spalling of a cover layer. Critical chloride concentration, loss of alkalinity and modeling of the steel corrosion are in researchers' spotlight for decades, however reinforcement corrosion in alkali activated materials is insufficiently described and understood yet.
In this work, the steel reinforcement corrosion in alkali-activated fly ash mortars is investigated in terms of electrochemical behaviour of the reinforced mortars exposed to aggressive environments such as leaching, carbonation and chloride ingress. A selected geopolymer mixture based on hard coal fly ash activated with sodium hydroxide and sodium silicate solutions is used for the steel reinforcement-corrosion experiments. The formation of passive layer on the steel rebars is observed after approx. two weeks of hardening at laboratory temperature. However, alternative heat-treatment at 80°C for several hours leads to immediate formation of the passive layer as well as to a faster strength gain (80 MPa after 24h at 80°C). Chloride-induced corrosion, leaching and carbonation resistance of the alkali activated fly ash-based concrete is studied, where leaching in deionized water or carbonation under natural conditions (~0.04 % CO2) for 300 days did not lead to corrosion of the embedded steel. On the other hand, accelerated carbonation under 100 % CO2 atmosphere lead to depassivation within two weeks.
The contribution reports on durability-related transport properties of geopolymer-based mortars. We show results of accelerated carbonation, rapid chloride migration (RCM), accelerated chloride diffusion, and air permeability measurements for fly ash-based geopolymer mortars, including mixes containing ground granulated blast furnace slag (GGBFS). In addition, we report polarization resistance data and corrosion potential vs. time curves for carbon steel bars embedded in two of the fly ash-based geopolymer mortars and a CEM I-based mortar (as reference).
Despite comparable total porosities, the carbonation depths, the chloride migration coefficients and the air permeabilities of the mortars differed significantly. In general, the addition of GGBFS to the binders improved the performance (decreased transport coefficients); however, this was not found to be true for the air permeability in all cases. This latter effect can be explained by drying damage of the C-(A-)S-H gel in GGBFS-containing binders. On the other hand, low transport coefficients can also be achieved by optimization of the binder formulation without the addition of GGBFS, which is also reflected in the material’s air permeability.
The corrosion potential vs. time curves in combination with polarization resistance values reveal that the steel reinforcement in geopolymer mortars assumed a passive state. However, this happened considerably later than for steel in CEM I-based mortars. The free corrosion potential of carbon steel reinforcement in the geopolymer mortars had different values than the free corrosion potential values for the CEM I-based mortar for both the active and the passive state.
In this article, we present a laboratory experiment to monitor the accelerated corrosion in concrete using ground-penetrating radar (GPR). Four concrete test specimens were cast with rebars of different size and placed at different depths. The lifetime decades of reinforcement corrosion process were accelerated into 18 days by using the impress current technique. The electrochemical corrosion process was periodically monitored with GPR. Two control specimens were also prepared to investigate the influence of chloride contamination on GPR signal. The measured data were analysed both in time and frequency domains. In time domain, the peak-to-peak amplitude of a wave reflected by a rebar was calculated to investigate the relationship between an increase in signal amplitude and the degree of corrosion. In frequency domain, the time–frequency representations of the signal were computed by using S-transform. The results show that reinforce corrosion increased the amplitude of reflected signal in time domain but did not change the peak frequency in frequency domain while chloride contamination attenuates the signal to smaller amplitude and lower peak frequency. Based on the results, a novel process is finally proposed for GPR-based corrosion detection.
Periodic mapping of reinforcement corrosion in intrusive chloride contaminated concrete with GPR
(2014)
This paper presents an experimental effort for developing a novel reinforcement corrosion monitoring technique based on Ground Penetrating Radar (GPR). Experiments were carried out to periodically monitor the accelerated reinforcement corrosion process with GPR. The data were processed in both time and timefrequency domains to investigate the tendencies of GPR signal attribute changes related with corrosion, moisture and chloride contamination. Data processing methods were proposed to visualize the reinforcement corrosion and chloride distribution with target specified signal attribute mapping. Half-Cell Potential (HCP) and Laser-Induced Breakdown Spectroscopy (LIBS) methods were employed to verify the GPR observations.
In this research, laboratory experiments were carried out to investigate the feasibility of using ground penetrating radar (GPR) for corrosion detection and/or monitoring, and the mechanism of corrosion caused GPR signal changes, taking into account the influence of several parameters: Chloride, rebar size and cover depth. With the understanding of the mechanism, a novel method for detecting reinforcement corrosion in concrete with GPR is proposed, together with a series of signal processing toolkits for corrosion visualization and image comparison.
The paper presents the damage model of German Research Unit 537 which was used as a working hypothesis for the development of a user-friendly design model. Excerpts from the laboratory experiments and numerical calculations processed in project A of the research unit are presented here. The excerpts include the quantification of self-corrosion, geometrical effects in the macrocell corrosion, development of corroding steel surface and pit depth as well as the quantification of the resistivity of the concrete and the corrosion of steel in cracked concrete.