Molten fluorides of alkali metals are considered a technological medium for molten salt reactors (MSRs). However, these media are known to be extremely corrosive. The successful implementation of high-temperature technological devices using molten alkali metal fluorides requires the selection of such structural materials that have high corrosion resistance in melts with compositional characteristic of MSRs. In this research, the corrosion behavior of 12Cr18Ni10Ti steel, the alloy Ni60Cr20Mo15, and the alloy Monel 404 (Ni50Cu50) was investigated in the LiF–NaF–KF eutectic melt, containing additions of CeF3 and NdF3 from 0 to 5 wt.% as imitator fluorides of actinides in an inert argon atmosphere at 550 °C for 100 h. Gravimetry, energy-dispersive X-ray (EDX) microanalysis of surfaces and cross-section of samples, and ICP-MS were used to establish the corrosion behavior of the investigated alloys. Corrosion resistance of the studied materials was found to decrease in a row from Monel 404 > Hastelloy C2000 > 12Cr18Ni10Ti. The addition of cerium fluoride into the melt resulted in the additional etching of the alloy surface. The addition of neodymium fluoride resulted in the formation of the point/inter-crystalline corrosion damages in the sample bulk. The samples of steel 12Cr18Ni10Ti were subjected to local cracking corrosion. The austenitic nickel-based alloys suffered specific local corrosion with formation of subsurface voids. Excellent corrosion resistance of the Monel alloy under the test conditions was found.
Composites of (1-x)Gd2Zr2O7·xMgO were prepared by mixing gadolinium zirconate with freshly precipitated Mg(OH)2 followed by heat treatment at 1500 °C. Small concentrations of magnesium oxide dissolved in the complex oxide matrix of Gd2Zr2O7. This led to decrease in the lattice parameters of the matrix phase and a complex redistribution of Gd and Zr over the A and B sublattices. According to the impedance spectroscopy results of the studied samples, for (1-x)Gd2Zr2O7·xMgO (x = 0.05, 0.07, 0.10), the ionic conductivity was slightly higher than that for the undoped Gd2Zr2O7. The share of dominant ion transport did not change upon doping with magnesium oxide. The composites showed chemical resistance in a lithium halide (LiCl) melt and interacted with LiCl-xLi2O (x = 2 wt.%, 4 wt.%) melts at 650 °C with the formation of a Gd2O3 phase or a mixture of phases (Gd2O3, Li2ZrO3, ZrO2, LiGdO2, or LiGdCl2) on the ceramic surface, respectively.
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