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The aim of this work is to quantify the corrosion kinetics of high-alumina refractories by a binary slag (Al 2 O 3 50 wt.% CaO 50 wt.%) and a ternary slag (Al 2 O 3 45 wt.% CaO 45 wt.% SiO 2 10 wt.%). The main objectives are i) to determine corrosion kinetics based on time-resolved X-ray diffraction at high temperature (1600 °C) combined with Rietveld quantification and (ii) to propose a reaction model based on the dissolution/precipitation/diffusion mechanisms. The results show that the corrosion process is very fast and involves an indirect dissolution mechanism with the formation of Al 2 O 3 /CA 6 /CA 2 /slag interfaces. [ABSTRACT FROM AUTHOR]

There is a growing interest in on-site, real-time analytical solutions for mining and environmental projects to characterize large areas and/or volumes of raw materials that are sometimes highly heterogeneous in terms of elemental distribution and mineralogy. Several fast and cost-effective methods are used for rapid on-site screening and real-time chemical and mineralogical characterization, such as portable X-ray fluorescence (pXRF) and X-ray diffraction (pXRD). However, these methods are not always applicable due to limitations in the detection and quantification of light elements (Mg, Al, Si) for pXRF or complex or minor minerals for pXRD, whose results need to be supported by laboratory analysis. This study presents a new methodological approach for in situ rapid chemical and mineralogical characterization of samples, based on the use of a transportable instrument (called ID2B) that allows, in a single acquisition step, a combined XRD-XRF analysis to identify and quantify the chemical elements and their associated minerals. The HI0 harzburgite sample from New Caledonia used to evaluate the data was analyzed in the laboratory (SEM-EDS, EPMA, XRF and XRD) and with the ID2B instrument to highlight the potential of our new methodology. In order to demonstrate the interest of using the ID2B combined XRF-XRD analysis approach directly in the field, where sample preparation is not always easy to implement, this comparison was made on the same sample (HI0), prepared in two different ways, either as a powderized (optimal preparation) or as-sawn (unprepared) sample. After automated processing of the combined XRF-XRD datasets acquired with the ID2B instrument, the chemical elements and mineralogical phases identified on both the powder and as-sawn samples are identical to the laboratory analyses. The chemical proportions calculated from the combined XRF-XRD data sets are also close to the laboratory XRF analysis with relative errors <5 % for Al, Mg and Si and even closer for Ca, Cr, Mn, Ni and Fe. The variability in the calculated chemical proportions is attributed to the sample heterogeneity highlighted by the mineral proportions that vary slightly between the laboratory XRD and XRD ID2B analyses of the powder, and more pronounced for the as-sawn XRD ID2B analysis. These observations show that the combined XRF-XRD approach performed on powder and as-sawn samples provides accurate chemical and mineralogical results to those obtained in the laboratory. The deployment of this new methodological approach directly on the field can provide valuable chemical and mineralogical analyses. • Field transportable XRF-DRX instrument for mineralogical and chemical quantification • Results from powder and as-sawn sample are quantitatively comparable. • Individual laboratory and combined XRF-XRD analyses provide very close results. [ABSTRACT FROM AUTHOR]