The application of organic coatings is a common way of protecting metal substrates against corrosion. To dry the coating faster, catalytic infrared radiation (IR) can be applied. This paper aims to assess the differences in the physical, chemical, and corrosion properties of primer coatings dried with catalytic infrared radiation, compared to the same coatings dried under atmospheric conditions. Corrosion properties were characterized using humidity and a salt spray chamber, as well as electrochemical impedance spectroscopy (EIS), preceded by open circuit potential (OCP) measurement. Pencil hardness, cross-cut, and pull-off adhesion tests were used to compare the properties of examined primers before and after testing in the corrosion acceleration chambers. The microstructure and distribution of chemical composition were studied by scanning electron microscope (SEM) with energy-dispersive X-ray spectroscopy (EDX) together with Fourier-transform infrared spectroscopy (FTIR). Phase transitions in the coating were determined by differential scanning calorimeter (DSC). Infrared-dried primers achieved a higher curing degree. Therefore, their mechanical and corrosion properties are superior when compared to the same coatings dried under atmospheric conditions.
Nanostructured cemented carbides with Co binders have shown excellent mechanical properties in various applications. Nevertheless, their corrosion resistance has shown to be insufficient in different corrosive environments, leading to premature tool failure. In this study, WC-based cemented carbide samples with different binders were produced using 9 wt% of FeNi or FeNiCo with the addition of Cr3C2 and NbC as the grain growth inhibitors. The samples were investigated using electrochemical corrosion techniques: the open circuit potential Ecorr, the linear polarization resistance (LPR), the Tafel extrapolation method, and the electrochemical impedance spectroscopy (EIS) at room temperature in the solution of 3.5% NaCl. Microstructure characterization, surface texture analysis, and instrumented indentation were conducted to investigate the influence of corrosion on the micro-mechanical properties and the surface characteristics of the samples before and after corrosion. The obtained results indicate a strong binder chemical composition's effect on the consolidated materials' corrosive behavior. Compared to the conventional WC-Co systems, a significantly improved corrosion resistance was observed for both alternative binder systems. The study shows that the samples with the FeNi binder are superior to those with the FeNiCo binder since they were almost unaffected when exposed to the acidic medium.
This paper presents the conformity assessment process of the epoxy coating thickness applied on water pipes made of gray cast iron with the specifications given for this kind of coating appliance. An epoxy coating was applied to prevent a special form of corrosion called the graphitization of cast iron. In order for the pipe to withstand its designed service life, it is necessary to ensure the required thickness of the applied coating. In accordance with the EN 877 norm, the thickness of the epoxy coating on the pipes for the projected corrosiveness of the environment C4 and the durability of 20 years is at least 70 µm and this indicates the required accuracy of the product. To achieve the desired product quality, statistical control of the coating application process was carried out and the impact of uncertainty associated with the measurement result was analyzed. Considering the quality of the coating application process and the quality of the measuring system, and to ensure the quality of products and to reduce consumer risk, the optimal thickness of the coating was determined.
Increasing attention is given to waterborne coatings for corrosion protection due to the lower ecological impact on the environment. It has been found that by using waterborne coatings, the emission of harmful volatile organic compounds (VOCs) is reduced by more than 50 g/L. However, they require longer drying time, their anti-corrosion performance is not as good as solvent-borne coatings and they still have not been developed for all corrosion environments. Another way to reduce VOCs is by using infrared (IR) drying technology. With catalytic infrared radiation, it is possible to cure all surfaces at notably reduced costs compared to traditional systems and in total respect for the environment, thanks to significant energy savings and minimal CO2 emissions. The aim of this paper was to evaluate corrosion protective properties of waterborne coatings which were dried with traditional and accelerated drying techniques, i.e., under atmospheric conditions and by using IR technology. Two different coating systems were applied, with and without Zn in the primer. To achieve this goal, the test samples were subjected to electrochemical, corrosion, and physical tests. It was shown that infrared technology does not affect the quality of the coating and it drastically reduces the intercoating interval. A coating system with zinc in the primer showed better overall protection properties after being subjected to impedance and salt spray testing, but generally, solvent-borne coatings still have higher durability than waterborne in extreme marine conditions according to recent research. Microstructure and porosity remained intact and the atomic force microscope confirmed that the flash-off was conducted correctly since there were no pinholes and blisters detected on the coating's surface. This study can serve as a foundation for further investigations of IC-dried waterborne coatings because there are not many at the moment.
The electrochemical corrosion resistance of nanostructured hardmetals with grain sizes dWC < 200 nm was researched concerning Co content and the chemical nature of the Co binder. Fully dense nanostructured hardmetals with the addition of grain growth inhibitors GGIs, VC and Cr3C2, and 5 wt.%Co, 10 wt.%Co, and 15 wt.%Co were developed by a one cycle sinter-HIP process. The samples were detailly characterized in terms of microstructural characteristics and researched in the solution of H2SO4 + CO2 by direct and alternative current techniques, including electrochemical impedance spectroscopy. Performed analysis revealed a homogeneous microstructure of equal and uniform grain size for different Co contents. The importance of GGIs content adjustment was established as a key factor of obtaining a homogeneous microstructure with WC grain size retained at the same values as in starting mixtures of different Co binder content. From the conducted research, Co content has shown to be the dominant influential factor governing electrochemical corrosion resistance of nanostructured hardmetals compared to the chemical composition of the Co binder and WC grain size. Negative values of Ecorr measured for 30 min in 96% H2SO4 + CO2 were obtained for all samples indicating material dissolution and instability in acidic solution. Higher values of Rp and lower values of icorr and vcorr were obtained for samples with lower Co content. In contrast, the anodic Tafel slope increases with increasing Co content which could be attributed to more pronounced oxidation of the higher Co content samples. Previously researched samples with the same composition but different chemical composition of the binder were introduced in the analysis. The chemical composition of the Co binder showed an influence; samples with lower relative magnetic saturation related to lower C content added to the starting mixtures and more W dissolved in the Co binder during the sintering process showed better corrosion resistance. WC-5Co sample with significantly lower magnetic saturation value showed approximately 30% lower corrosion rate. WC-10Co sample with slightly lower relative magnetic saturation value and showed approximately 10% lower corrosion rate. Higher content of Cr3C2 dissolved in the binder contributed to a lower corrosion rate. Slight VC increase did not contribute to corrosion resistance. Superior corrosion resistance is attributed to W and C dissolved in the Co binder, lower magnetic saturation, or WC grain size of the sintered sample.
