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Agar gel pads have been used for electrochemical measurements for some time. For zinc in particular, a standard method for measuring the stability of the corrosion product layer is being established. The main interpretation factor is the corrosion product layer resistance RL, as it is easy to determine and interpret. A high corrosion product layer resistance indicates a high level of protection. However, it is not yet known how low the corrosion product layer resistance is for freshly produced zinc samples. As zinc is highly active, it reacts immediately with the environment to form a corrosion product layer, which affects the corrosion product layer resistance. The addition of zinc acetate to the agar gel pads prevents the formation of a surface layer and destroys existing ones.
This makes it possible to measure an almost corrosion product-free zinc surface. This is important in defining the range of corrosion product layer resistance for a protective surface.
Literature data on the influence of concrete cracks on corrosion propagation of reinforcing steel are contradictory. This might be due to very different exposure and test conditions but also to a lack of time-resolved data in cyclic wetting–drying exposure. Here, the influence of the environmental conditions on the corrosion rates in cracked concrete is studied experimentally. The results show that the corrosion rate in cracked concrete depends on the duration of wetting and drying phases and the relative humidity (RH) during the drying phase. The lower the ambient RH in the drying phase, the faster the cracks dry, which depresses the corrosion rate in the periods between the wetting events. A model is proposed to estimate corrosion rates in cracked concrete cyclic wetting/drying exposure.
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.
The second part of this paper looks continues the comparative investigation of lean duplex stainless steels, manganese alloyed austenitic and duplex stainless steels and ferritic stainless steels. These new materials were investigated in many different test procedures and in different conditions focused on the application in civil engineering and common use. In addition to electrochemical investigations, all materials were exposed to atmospheric conditions in different surface states. In Part 2, Prof. Gümpel and his team examine the effects of coastal and urban atmospheres on the samples, and presents their final conclusions.
Rising prices of nickel and molybdenum in the recent past years have led to unprecedented interest in substituting leaner-content alloys for standard 300-series austenitic stainless steels in many applications. Due to the price volatility of various alloying elements, many new materials have entered the market, yet no direct comparison of corrosion resistance of these new materials exists. In this project, comparative investigations were carried out and in each case one or several representatives of a material group were taken into account. The material groups covered were: lean duplex stainless steels, manganese alloyed austenitic and duplex stainless steels and ferritic stainless steels. In addition to electrochemical investigations, all materials were exposed to various atmospheric conditions in different surface states.
In addition to constructional requirements in civil engineering stainless steels often have to fulfil high visual demands. Unexpected impairments of the visual appearance of stainless steels under low corrosive conditions are a widespread problem today. Frequently it is supposed that this is caused by changes in the alloy composition, worse environmental conditions or improper handling. Within a research project the systematic investigation of several cases of damaged stainless steel bars has shown that the reasons are based on well-known material defects like chemical inhomogeneities (e.g. precipitations or local carburization) or geometrical defects (e.g. undercuts, rolling defects or shell formation). Thus, the failures could be clearly identified as production failures of the respective semi-finished products.
An unusual feature known as the negative difference effect (NDE) can be observed in magnesium when recording corrosion current density–potential curves. More hydrogen is evolved at a more positive potential which does not occur in conventional metals. Several models have been proposed in the literature in order to explain the phenomenon of NDE. They succeed in explaining some effects, and fail to deal with others. A new model, which explains the NDE by two electron consuming processes, is presented in this paper. By potentiostatic investigations of magnesium in a chloride electrolyte, measurements of hydrogen evolution and chemical analysis of the electrolyte the new model was experimentally verified.
Investigations have been carried out on an erosion-corrosion apparatus to investigate the behaviour of corrosion-resistant highalloy iron-base materials containing hard phases. These materials had been optimized for increased wear resistance under complex stress conditions. As expected, in dry erosion tests, very low mass losses were established; there was little difference between the materials. Also, in corrosive environments (NaCl, H2SO4), the materials showed good stability; however, the duplex structures were superior to the martensitic ones. The combination of erosion and corrosion produced large differences and, in some cases, markedly reduced resistance to damage. These results confirmed observations that it is impossible to deduce the environmentally influenced mechanical behaviour of an alloy from its behaviour in separate corrosion and erosion experiments. The basic mechanisms underlying these processes have been investigated only tentatively.