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Eingeladener Vortrag
- nein (191)
Although zinc and zinc coatings have been widely used for corrosion protection for decades new zinc coatings are constantly being developed. Characterizing the corrosion protectiveness of these new coatings, however, should not be underestimated. While exposure tests are time intensive, cyclic tests can only be used for a very limited field of application. Thus, electrochemical measurements provide both an efficient and an effective alternative. Conventional aqueous bulk electrolytes influence the surface layers of a tested zinc coating and are therefore not reliable. Gel electrolytes, however, have evolved over the last few years, are minimally invasive and provide reliable results.
This work describes experiments with gel electrolytes made of agar. Unlike previous work, it proposes a composition of gel electrolyte for minimally invasive description of the protective power of naturally formed oxide layers on zinc and zinc coatings. Therefore, as a first part, the gel electrolyte made of agar is verified as a method for zinc and zinc-coated samples. Afterwards, this paper introduces the corrosion product layer resistance RL as a promising parameter to evaluate the protective power of zinc coatings. Results are verified with EIS and FTIR measurements. An example on a representative zinc coating demonstrates the practical application.
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.
Hot cracks as stress corrosion cracking initiation sites in laser welded corrosion resistant alloys
(2005)
Although hot cracks at weld surfaces of corrosion resistant alloys (CRAs) might provide access to respective aggressive media and thus, might provide the conditions for a local potential and pH drop, the interaction between hot cracking and corrosion phenomena has not been investigated up to the present. This particularly concerns the initiation of stress corrosion cracking inside such crevices.
As a first approach to clarify the influence of hot cracks on corrosion resistance, considering particularly stress corrosion cracking, hot crack afflicted laser welds of three different CRAs have been subjected to a series of different corrosion tests.
Besides the fact that the Drop Evaporation (DE) Test represents a more realistic procedure than standard immersion tests it turned out that hot cracks can obviously represent an initiation site of stress corrosion cracking in the austenitic stainless steel AISI 309 (German No. 1.4828). The susceptibility of such hot crack afflicted laser welds to stress corrosion cracking (SCC) significantly depends on temperature and chloride concentration of the test environment In comparison, the high nitrogen austenitic stainless steel AISI S 34565 (German No. 1.4565) did not exhibit any stress corrosion cracking associated with hot cracking. This material exhibited pitting corrosion and stress corrosion only in the base material. The Alloy 50 (German No. 2.4850), a Nickel based material, was susceptible to pitting corrosion, but showed no tendency towards stress corrosion cracking at all.
Electrochemical noise (EN) enables corrosion research and monitoring in real time and with high sensitivity. In the case of submicroscopic nucleation events of pitting corrosion it has been observed that the cathodic process plays a decisive role in the mechanism as well as in the origin of EN signals, which depend not only on the metallic dissolution reaction but also on the electron-consuming process. EN signals arising from the nucleation process of localized corrosion on stainless steels can only be recorded due to the inhibition effect on the cathodic process achieved by the spontaneous formation of the passive layer. In consequence, passive layer stability becomes a significant factor in influencing EN signals. The way in which the passive layer stability affects the acquisition and analysis of EN signals arising from pitting corrosion on stainless steels is discussed in detail.
Unwanted corrosive phenomena on stainless steel surfaces like rouging had been observed for years occurring at certain service conditions. Rouging consists in the formation of a colored surface film containing mainly iron on metallic surfaces in contact with high-purity waters. In spite of numerous hypotheses and experimental examinations a clear explanation about the origin of rouging on stainless steels is currently still lacking. Because rouging occurs even at well passivated stainless steel surfaces the origin of this corrosive phenomenon should be related to the weakness of the stability of the passive film. In the present paper electrochemical noise measurements regarding the stability of the passive layer of alloy 904L (1.4539, X1NiCrMoCu25-20-5) in high-purity water at 70 °C depending on the cathodic process are presented. In addition, the importance of the cathodic reaction on the passivation and stability of the passive layer is discussed.
Electrochemical noise measurements on anodically polarised type 304 stainless steel surfaces in contact with buffer solutions of neutral pH were performed to study the effect of chloride ions in the nucleation of pitting corrosion. Passive layer stability and susceptibility to pitting corrosion after pickling and passivation at different environmental conditions were also investigated by means of electrochemical current noise measurements under cathodic and anodic polarisation. According to the obtained experimental results pits nucleate independently on the presence of chloride ions. It has been also shown that protectiveness of stainless steel surfaces after pickling strongly depends on the relative humidity of the environment in which the surface is subsequently passivated.
Recent progress in the qualification of materials used in geothermal energy conversion systems
(2010)
The corrosion resistance of stainless-steels grades is of high importance for the technical safety in different environmental conditions. Processing and surface finish influences the corrosion resistance of ferritic stainless steels, which may be considered for some application in marine environment. Three ferritic stainless steel alloys (X2CrNi12, X2CrTiNb18 and X2CrMoTi18-2) were exposed in four different surface finishes (rolled, dry grinding, glass beaded and electro polished) for five years in marine environment to obtain reliable information about the corrosion resistance. All samples were assessed after 22 and 60 months according to DIN EN ISO 10289 in validation degrees from 1 to 10. Complementary investigation using accelerated chamber test (salt spray test followed by four weeks storage at 30 °C / 80 % relative humidity) and short-term electrochemical methods (electrochemical potentiodynamic reactivation, pitting potentials and the KorroPad method) were conducted to compare their results. The presentation gives an overview on all methods and the generated results, which show benefits and restrictions of long-term, accelerated and short-term corrosion tests.
Samples of the austenitic stainless steel grade X5CrNi18‐10 (1.4301, AISI 304) were ground industrially with various grinding parameters to study their influence on corrosion resistance. The ability of the mechanically ground surfaces to form a stable passive layer was evaluated by KorroPad test and a modified electrochemical potentiodynamic reactivation test based on a single loop (EPR‐SL). Furthermore, the surfaces were characterized by surface analytical methods. The main influence was determined regarding abrasive belt type. Surfaces mechanically ground with granulate abrasive belts constantly had a lower corrosion resistance than surfaces ground with single‐coated grain. The granulate abrasive belts generated more sensitized surface areas and left formations of welded sample material on the mechanically ground surfaces. A post‐treatment with a nonwoven abrasive proved to be an effective finishing process by which the surface defects and sensitized material got removed and the surfaces regained the expected corrosion resistance.