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The reduction of the chromate contents in cements affects the electrochemical reactions of galvanized reinforcing steels in fresh concrete. By means of electrochemical measurements and bar pull-out tests the effect of chromates on the formation of protective coatings at the zinc and the bond behaviour have been investigated using chromate-containing and chromate-reduced cements. The results have shown that the bond zone was affected as a result of chromate reduction for cement types CEM I and CEM II. The disturbance to the bond zone should be considered as long-term in relation to the pore structure which is formed. The effects on the bond are largely compensated for as the concrete ages. The results of the related bond strength with displacement paths of 0.1 and 0.5?mm, respectively, are still within the range of expected figures for non-galvanized reinforcing steel despite the structural disturbance. Under practical aspects it is not necessary that the existing structural disturbance with respect to bond strength is taken into consideration.
Korrosions- und Verbundverhalten verzinkter Betonstähle in Betonen mit chromatreduzierten Zementen
(2011)
Durch die Absenkung des Chromatgehalts der Zemente verändern sich die elektrochemischen Reaktionen von verzinkten Betonstählen in der Frischbetonphase. Mit Hilfe von elektrochemischen Messungen sowie Stabauszugsversuchen wurde an chromathaltigen und chromatreduzierten Zementen die Auswirkung des Chromats auf die Deckschichtbildung am Zink und auf das Verbundverhalten untersucht.
Mit den Ergebnissen konnte eine Beeinträchtigung der Verbundzone als Folge der Chromatreduzierung für die Zementarten CEM I und CEM II nachgewiesen werden. Die Störung der Verbundzone ist in Bezug auf die sich ausbildende Porenstruktur als dauerhaft anzusehen. Die Auswirkungen auf das Verbundverhalten werden mit zunehmendem Betonalter weitgehend kompensiert. Die Ergebnisse der bezogenen Verbundspannung bei Verschiebewegen von 0,1 mm und 0,5 mm liegen trotz der Gefügestörung noch im Bereich der Erwartungswerte für den unverzinkten Betonstahl. Unter baupraktischen Gesichtspunkten muss die auftretende Gefügestörung hinsichtlich der Verbundspannung daher keine Berücksichtigung finden.
Electrochemical potential mapping according to guideline B3 of DGZfP (German Society for Nondestructive Testing) is a recognized technique for the localization of corroding reinforcing steels. In reinforced concrete structures the measured potentials are not necessarily directly linked to the corrosion likelihood of the reinforcing steel. The measured values may be significantly affected, different from, e.g., stress measurement, by different influences on the potential formation at the phase boundary metal/concrete itself as well as the acquisition procedure. Due to the complexity of influencing factors there is a risk that the results are misinterpreted. Therefore, in a training concept firstly the theoretical basics of the test method should be imparted. Then, frequently occurring practical situations of various influencing factors will be made accessible to the participants by a model object specially designed for this purpose. The aim is to impart profound knowledge concerning the characteristics of potential mapping for detecting corrosion of reinforcing steel in order to apply this technique in practice as reliable and economical test method.
Steel in concrete is protected by the alkaline pore water environment and the resulting formation of a protective passive layer against corrosion. Adverse environmental conditions due to carbonation or chloride ingress can destroy the passive layer on the steel surface. Corrosion processes starting in those areas lead to uniform corrosion or local corrosion like pitting corrosion. In comparison to uniform corrosion pitting corrosion is a form of increased local corrosion and thus leads to a progressive reduction in cross-section of the reinforcing steel. The corrosion products are first absorbed by the pores of the concrete matrix, without causing visible external changes at the concrete surface.
Carbon‐based conductive coatings are complex composites, consisting of an organic or inorganic binder and conductive carbon components, for application as anodes in impressed current cathodic protection systems of reinforced concrete structures. The electrochemical properties of three coatings at different humidity and in saturated calcium hydroxide solution were studied by electrochemical methods, such as electrochemical impedance measurement, measuring of open circuit potential over time and galvanostatic polarization. The dissolved organic and inorganic carbons in electrolyte solution were quantified by using a photometric method. The structures of the coatings were investigated before and after the electrochemical tests by microscopy and scanning electron microscope/EDX analysis. The results of the electrochemical impedance measurements show that the tested coatings all have a relatively low resistance, which is between 100 and 200V. The binder and the surface porosity influence the degradation behavior of those coatings. Especially the organic binder reacts with the strong alkaline medium under dissolving of organic carbon.
Aufgrund der in den letzten Jahren stark angestiegenen Rohstoffpreise sind die im Bauwesen häufig eingesetzten nichtrostenden Standardaustenite in vielen Fällen nicht mehr wettbewerbsfähig. Eine deutlich kostengünstigere Alternative stellt der Duplex-Stahl 1.4362 dar, der bisher aber noch nicht bauaufsichtlich zugelassen ist. Mit Hilfe von Auslagerungsversuchen sowie elektrochemischen Untersuchungen sollte das Korrosionsverhalten dieses Werkstoffs unter neutralen bis leicht sauren, chloridhaltigen Umgebungsbedingungen, wie sie in vielen Bereichen des Bauwesens vorkommen, geklärt werden. Insgesamt belegen die Ergebnisse, dass der kostengünstigere Werkstoff 1.4362 für baupraktische Anwendungen eine Alternative für Anwendungen darstellen kann, in denen bisher die Werkstoffe 1.4404 oder 1.4571 eingesetzt wurden.
In indoor swimming pools stainless steels are used not only due to structural and economic reasons but also due to aesthetic considerations. And therefore not only safety relevant load bearing components have to fulfil their tasks but also the visual appearance should be free of any staining. In a lot of cases basic requirements (e.g. design criteria, material selection and maintenance) being essential parts of technical regulations were not taken into account. Typical case studies with explanation of the cause of the corrosion problems and possibilities to prevent them are shown in the present paper.
Chloride contents at the steel–mortar interface that initiate steel corrosion were determined for carbon steel in alkali‐activated fly ash mortar for three different exposure conditions: exposure to 1 M NaCl solution; leaching in deionized water and then exposure to 1 M NaCl solution; and leaching in deionized water, aging in air at 20°C and natural CO2 concentration, and then exposure to 1 M NaCl solution. For comparison, a Portland cement mortar, exposed to 1 M NaCl solution, was studied. The median values of the corrosion‐initiating chloride contents (average over the full length of the rebar) in the alkali‐activated fly ash mortar varied between 0.35 and 1.05 wt% Cl with respect to binder, consistently lower than what was obtained for the Portland cement mortar, but with no clear trend regarding the exposure conditions. For most of the alkali‐activated fly ash mortar specimens, preferential corrosion at the connection between the working electrode and the external measurement setup was observed, while preferential corrosion did not occur for the Portland cement mortar. Scanning electron microscopy and auxiliary experiments in synthetic solutions indicated that this behavior was caused by inhomogeneities at the steel–mortar interface in the alkali‐activated mortar, likely due to its peculiar rheological properties in the fresh state.
Alkali-activated fly ash mortars were studied with regard to durability-relevant transport coefficients and the electrochemical behaviour of embedded carbon steel bars on exposure of the mortars to leaching, carbonation and chloride penetration environments. The transport coefficients differed considerably between different formulations, being lowest for a mortar with BFS addition, but still acceptable for one of the purely fly ash-based mortars. Leaching over a period of ~300 days in de-ionized water did not lead to observable corrosion of the embedded steel, as shown by the electrochemical data and visual inspection of the steel. Exposure to 100 % CO2 atmosphere caused steel depassivation within approx. two weeks; in addition, indications of a deterioration of the mortar were observed. The results are discussed in the context of the different reaction products expected in high- and low-Ca alkali-activated binders, and the alterations caused by leaching and carbonation.