Two tristructural isotropic (TRISO)-coated nuclear fuel particles were examined by electron probe microanalysis (EPMA) as part of the Advanced Gas Reactor program. The compacts’ average irradiation temperatures ranged from approximately 1260 to 1290 °C. One particle was examined in the as-irradiated condition, while the other was subject to 1600 °C post-irradiation safety testing. This study was undertaken to test a newly-developed EPMA technique to determine fission product masses in TRISO particles on a layer-by-layer basis, and to compare fission product distributions between an as-irradiated and safety-tested particle. Fission product concentration profiles were collected along two radii in each particle, with measured concentrations used to compute the fission product mass in each TRISO particle layer. These measured masses were then compared to those predicted from ORIGEN modeling calculations. Data collected from these measurements show that for these two particles, masses determined via EPMA were within ± 20% of the calculated masses for the rare-earth elements, Mo, Zr, Cs, I, and Pd. Elements that tend to be less homogeneously distributed include Sr, Te, Eu, Ag, and possibly Ba. Measured Ag masses differed by more than 40% from the calculated mass. Lanthanides other than Eu remain primarily within the fuel kernel in the as-irradiated particle but in the safety-tested particle these element masses were divided approximately equally between the kernel and kernel periphery. In both particles, the majority of Sr and Eu accumulated in the carbon-rich kernel periphery, although in the safety-tested particle, Sr and Eu accumulated farther from the fuel kernel than occurred with irradiation alone. A greater mass fraction of mobile elements, such as Cs and I accumulated in the buffer and IPyC in the safety-tested particle as compared to the as-irradiated particle. When fully developed and tested, this mass balance approach to TRISO particle analysis has the potential to provide insight into fuel behavior.

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This paper presents experimental investigations into the effects of ultrafine blast furnace slag on microstructure improvements against chloride penetration in saturated and unsaturated cementitious systems exposed to cyclic drying–wetting conditions. The hydration kinetics of ultrafine slag powders and pore solution chemistry in slag-blended cementitious systems at different ages, together with the main hydration products and pore structure characteristics, were determined. The chloride profiles accounting for different slag contents and drying–wetting cycles were measured. The results reveal that the reactivity of ultrafine slag can be well described with Avrami’s equation. The dilution effect of the slag predominated the pore solution chemistry, and the pH value decreased with a higher inclusion of slag. An optimal inclusion of 65% slag by mass of the binder corresponding to the finest pore structure and highest hydrotalcite content was found, which provides a reasonable basis for the slow chloride diffusion and high chloride binding. Under drying–wetting exposure, the specimen with a lower saturation exhibited a higher chloride transport caused by capillary absorption in the skin layer. The chloride transport tended to be diffusion controlled after sufficient drying–wetting cycles@en