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- Cathodic protection (4)
- Steel in concrete (3)
- Cathodic Protection (2)
- Concrete (2)
- Concrete parameters (2)
- Self-corrosion (2)
- X-ray tomography (2)
- Carbon steel (1)
- Chloride Induced Corrosion (1)
- Chloride Migration (1)
Long-term experiences with cathodic corrosion protection of steel reinforced concrete structures
(2002)
Cathodic protection (CP) is a common method for rehabilitation of reinforced concrete structures suffering from Chloride induced corrosion. A sufficient protection of the corroding rebar can be ensured by use of several protection criteria. The use of these assessment criteria, in particular the so called 100 mV-criterion, can lead to erroneous resuits for certain unconventional arrangements of rebar and cp anode.
Therefore a joint research project of the Institute for Building Materials Research, RWTH-Aachen University, Germany, (ibac) and the Federal Institute for Materials Research and Testing, Berlin, Germany, (BAM) has been set up to determine the applicability of CP under arbitrary geometrical conditions. A special focus was set on the applicability of surface applied anode Systems for protection of the reinforcement of structures opposite to the accessible side (e.g. outer side of tunnel Shell, Bridge deck protected from inside a box girder) In this paper, the impact of the time dependent changes of the Polarisation behaviour of the rebar on the current and potential distribution is shown by means of parametric studies using the FEM method.
Corrosion of steel reinforcement in concrete exposed to chloride containing environments is a serious problem in civil engineering practice. The standards and guidelines contain only minimum requirements regarding concrete quality and concrete cover. In very critical cases, for example the ingress of chlorides, the application of different coatings is currently the only possibility to protect the reinforced concrete structures. In this case the modelling of reinforcement corrosion would be more practical. One sub-project of a DFG-research project (FOR 537) is currently performed at the Federal Institute for Materials Research and Testing (BAM). Aim of the sub-project is the description of corrosion propagation and the characterization of the corrosion on specimens with small and large cathodes, by electrochemical parameters. The electrochemical parameters are determined by suitable electrochemical measurements, considering concrete parameters as well as different environmental conditions.
Pitting corrosion of carbon steel and iron in chloride containing alkaline environment is already well investigated, although a couple of questions are not clarified satisfactorily. The critical chloride content for steel in concrete and the critical chloride to hydroxide ion ratio for steel in alkaline solutions is still a major concern, considering chloride induced corrosion problems of steel in concrete. Another not satisfactorily clarified point is the repassivation of carbon steel in consequence of cathodic polarization. In the recent literature some indications are shown that repassivation occurs after a certain time of polarization. GLASS [4-9] and PEDEFERRI [1-3] draw the conclusion that the ennoblement of open circuit potentials (OCP) indicates re-passivation effects due to cathodic polarization. SAGÜÉS [10] carried out potentiodynamic repassivation tests and draws the conclusion that the repassivation potential Er is nearly independent of the solution composition, but influenced by severity of corrosion attack and is in the potential range from - 0.8 V to - 0.4 V vs. Saturated Calomel Electrode (SCE). The transferability of SAGÜÉS results to questions concerning cathodic protection (cp) is questionable, as potentiodynamic polarization tests (PPT) give no information on changes induced by long time polarization.
Therefore, the investigations discussed in this paper aim to clarify, to what extend the re-passivation of carbon steel due to cathodic polarization occurs, and if the ennoblement of OCP is a sufficient indication for repassivation. In a first step the corrosion state of five nominal equal test specimens was determined by electrochemical techniques, i.e. electrochemical noise measurements (ENM) and electrochemical impedance spectroscopy (EIS). After determining the initial corrosion state by evaluating the charge transfer resistance and the polarization resistance respectively as well as evaluating potential and current noise signals, the specimens were polarized cathodically. Impedance data were recorded previous to, during and after polarization. The impedance data were evaluated by equivalent circuit fitting with special attention to charge transfer resistances and diffusion properties. The results show that reduction of oxides and oxygen diffusion during cathodic polarization has strong impact on the systems behavior.
Corrosion of steel reinforcement in concrete exposed to chloride containing
environments is a serious problem in civil engineering practice. Electrochemical
methods, e.g. potential mapping, provide information whether the steel reinforcement
is still passive or depassivation has been initiated. By applying such techniques no
information on the type of corrosion, its extent and distribution of corrosion products
is available. Particular the corrosion progress is a significant problem. Especially in
the case of element corrosion in reinforced concrete structures, the development at
the anode can not be separated into corrosion damage causing by element corrosion
or self-corrosion. Until now also in laboratory tests it is impossible to collect such
information without destroying specimens after electrochemical testing was
performed place. To overcome this problem it was tried to study the steel surface
within the mortar specimens by X-ray tomography (CT). Within the scope of these
investigations it could be shown, that X-ray tomography is suitable to make corrosion
pits visible which are embedded in a mortar with a cover thickness of about 35 mm.
In this publication the corrosion damage of reinforced steel is documented timedependent
by X-ray tomography.
A joint research project was accomplished by ibac and BAM with the aim to develop a numerical model
of cathodic protection (CP) of reinforced concrete with a special focus on CP of the rear reinforcement
layer. The model was intended to include the effects of chemical alterations within the concrete and the
steel concrete interface, which are induced by long-term application of CP. The investigations presented
in this paper focus on the migration of chloride ions due to small electric fields as applied during cathodic
protection of steel in reinforced concrete structures and its impact on polarisation characteristics. A
comparatively new method, laser induced breakdown spectroscopy (LIBS), was used to determine
chloride profiles on laboratory specimens in order to investigate one of several model parameters to
describe cathodic protection of the rear reinforcement of reinforced concrete structures. These
investigations are described elsewhere, [1].
The paper focuses on long term polarisation tests and their impact on the charge depending cathodic
polarisation behaviour of laboratory specimens.