The aim of this review is to summarize the possibilities of replacing graphite bipolar plates in fuel-cells. The review is mostly focused on metallic bipolar plates, which benefit from many properties required for fuel cells, viz. good mechanical properties, thermal and electrical conductivity, availability, and others. The main disadvantage of metals is that their corrosion resistance in the fuel-cell environment originates from the formation of a passive layer, which significantly increases interfacial contact resistance. Suitable coating systems prepared by a proper deposition method are eventually able to compensate for this disadvantage and make the replacement of graphite bipolar plates possible. This review compares coatings, materials, and deposition methods based on electrochemical measurements and contact resistance properties with respect to achieving appropriate parameters established by the DOE as objectives for 2020. An extraordinary number of studies have been performed, but only a minority of them provided promising results. One of these is the nanocrystalline β-Nb₂N coating on AISI 430, prepared by the disproportionation reaction of Nb(IV) in molten salt, which satisfied the DOE 2020 objectives in terms of corrosion resistance and interfacial contact resistance. From other studies, TiN, CrN, NbC, TiC, or amorphous carbon-based coatings seem to be promising. This paper is novel in extracting important aspects for future studies and methods for testing the properties of metallic materials and factors affecting monitoring characteristics and parameters.

The Czech Republic has a well-developed nuclear programme with two nuclear power plants currently in operation and three operational near-surface repositories serving for the disposal of institutional and operational low- and intermediate-level waste. Spent nuclear fuel will be disposed of in a deep geological repository to be constructed in crystalline or metamorphic rock approximately 500 m below the surface. Czech Ca–Mg bentonites will be used as the buffer and backfilling material. Steel-based materials are currently considered as the reference metallic materials in the Czech disposal canister concept. The preferred design is based on a double-walled canister with an inner shell of stainless steel and an outer shell of carbon-steel. Both parts of the canister must provide mechanical stability; the wall of the carbon-steel canister will be strengthened for corrosion-resistance purposes. The presented work focuses on canister design as confirmed by means of mechanical, thermal and criticality calculations and a detailed experimental corrosion plan. This paper is part of a supplement on the 6th International Workshop on Long-Term Prediction of Corrosion Damage in Nuclear Waste Systems.

Sixteen localities were involved in a broad study, resulting in the classification of the indoor corrosivity of metals considered in the ISO 11844 standard, especially lead. Recently, lead has been added to the standard as a metal specifically sensitive to volatile organic compounds such as acetic acid. Data on one-year exposure in museum depositories and exhibition spaces, archives, libraries, and churches show that the currently valid lead corrosivity categories are not correctly defined. The obtained data allowed for the proposal of new realistic ranges of indoor corrosivity categories for lead. The exposure program was also used to validate techniques for determining the corrosion degradation of metal coupons. Mass increase and mass loss techniques were supplemented with the galvanostatic reduction technique and the measurement of color changes. The study identified the limitations of the mass gain method. Not only is the galvanostatic reduction technique applicable for silver and copper coupons, but the build-up of reducible lead corrosion products depends on air corrosivity. CIELab color-change measurement has proven to be a simple and easy-to-apply method for monitoring the corrosivity of indoor atmospheres with regard to lead. A more reliable response is provided by the determination of color change after 3 months of exposure rather than after one year.

This paper studies the effect of water as an oxidation agent and also of oxygen on zinc corrosion kinetics in active state in concrete, using high-sensitivity electrical resistance sensors. It was proven that zinc corrosion in active state is strongly affected by the presence of water at its surface. Zinc corrosion in real concrete in the absence of water can be misinterpreted as salt passivity. The presence of oxygen results in an increase of zinc corrosion rate, however at pH 12.6, passivity can occur. It was verified that corrosion products consisting primarily of Ca[Zn(OH)₃]₂·2H₂O cannot effectively passivate zinc surface in concrete, even after 1800 h of exposure and zinc, or hot-dip galvanized steel can corrode at an unacceptable corrosion rate (more than 4 µm·a⁻¹).

This article provides a comprehensive overview of the potential use of organofunctional silane coatings in the corrosion protection of concrete reinforcement in close relation to other commercially used coating technologies—i.e., epoxy coatings and bath hot-dip galvanizing coatings. The application technology of the steel surface is described in detail, and the corrosion performance and bond strength in concrete are compared. The paper also points out the possibility of improving the durability of epoxy coatings by the addition of silanes and, in the case of application to the surface of hot-dip galvanized steel, they can prevent corrosion of the coating by hydrogen evolution. The application potential of organofunctional silanes is also presented in the form of hydrophobic coatings on concrete surfaces or as corrosion inhibitors in simulated concrete pore solutions. The use of a suitable type of modified silane coating on the surface of carbon steel reinforcement can increase the corrosion performance and can also increase the bond strength in concrete. However, these facts need to be experimentally verified.