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Epoxy-based intumescent coatings are effective solutions for protecting steel against fire. To design a successful product, it is, however, of primary importance to investigate its long-term durability. Some of these coatings do not resist accelerated aging conditions such as contact with salted water. One solution to overcome this drawback consists of applying a specific topcoat. In this work, various topcoats were applied on a model intumescent coating. Topcoats were shown to impact, under heating, the char expansion, char morphology, and char strength. The general trend is that the topcoats, before any aging exposure, improve the fire resistance behavior of the intumescent coatings. Most topcoats, however, do not limit penetration of salted water into the coating, thus affecting the intumescent properties. Only a silane-based topcoat was reported to trap or limit the diffusion of sodium and chlorine ions, thus protecting the underlying intumescent coating.

International audience; Using XRD, impedance spectroscopy, and XPS, it was shown that both Bi2Ru2O7 and Pb2Ru2O6.5, generally announced as attractive electrode materials for IT-SOFCs, chemically react with CGO. In addition, a never-mentioned time-instability under electrochemical measurements with YZS as electrolyte mediates the polarization tests. For Pb2Ru2O6.5, long time experiments (stabilization time > 900 h, previously to complementary electrochemical tests), yields strong increasing of the resistance polarization. Concerning Bi2Ru2O7, a partial transformation into Bi3Ru3O11 is observed after impedance measurements. The investigation of the Bi2−xMxRu2O7−δ (M = Sr, Pb) solid solutions was performed with the aim to improve the catalytic/electric properties. For low x values, it shows a time and chemical stabilization of the electrode/electrolyte cells, able to preserve high electrode performances of these materials. For higher substitution, the chemical/electrochemical instability reappears. According to our polarization measurements versus oxygen pressure and temperature in the so-called “stabilized” samples, the electrode performance appears limited by the diffusion of adsorbed oxygen on the triple point boundary. It is fully compatible with the metallic behavior checked in all the series.

Luminescent ionogels were prepared by doping an europium(III) tetrakis β-diketonate complex into an imidazolium ionic liquid, followed by immobilization of the ionic liquid by confinement in a silica network. The ionogels were obtained by a non-hydrolytic method as perfect monoliths featuring both the transparency of silica and the ionic conductivity performances of ionic liquids. The ionogels contain 80 vol % of ionic liquid. The organic−inorganic hybrid materials showed a very intense red photoluminescence under ultraviolet irradiation. The red emission has a very high coloric purity.

A simple nonaqueous sol−gel processing led to ionogels, resulting in the confinement of an ionic liquid within a silica-like network. In the case of a non-water-soluble ionic liquid, ionogels were made stable toward water immersion by the presence of hydrophobic methyl groups in the solid network. A set of ionogels with different ionic liquid content was studied by DSC and 1H NMR spectroscopy. The nanometric level of the confinement of the ionic liquid turned out to significantly modify the phase transitions, while still allowing some molecular mobility. Moreover, ionogels were found to keep the high conducting performances of the ionic liquid.