Bentonite is a claystone formed by a complex mineralogical mixture, composed of montmorillonite, illite, and accessory minerals like quartz, cristobalite, feldspars, carbonates, and minor amounts of iron oxy-hydroxides. Bentonite presents complexity at various scales: (1): a single mineral may present different chemical composition within the same quarry (e.g., feldspars solid solutions); (2): montmorillonite presents variability in the cation-exchange distribution while illite may be presented as mixed-layer with smectite sheets; and (3): hardness and crystal size are larger in accessory minerals than in clay minerals, preventing uniform grinding of bentonite. The FEBEX bentonite used is originally from Almería (Spain), and it is a predominantly calcium, magnesium, and sodium bentonite. This Spanish FEBEX bentonite has been hydrothermally altered at laboratory scale for 7–14 years. A thermal gradient was generated by heating a disk of pressed iron powder, simulating the metal waste canister, in contact with the compacted bentonite sample. Hydration was forced from the opposite direction. XRD recorded patterns were very similar. In order to minimize the bias of XRD semi-quantitative determination methods, Rietveld refinement was performed using BGMN software and different structural models. Confidence in the quantification of the main phases allows us to convincingly detect other subtle changes such as the presence of calcite in the hydration front, right at the interface between the saturated and unsaturated bentonite, or the presence of goethite, and not hematite, in the saturated bentonite, near the source of hydration. Smectite component was 72 ± 3% and the refinement was consistent with the presence of ~10% illite, comparable with previous characterizations.

Despite the multiple impacts of mineral aerosols on global and regional climate and the primary climatic control on atmospheric dust fluxes, dust-climate feedbacks remain poorly constrained, particularly at submillennial time scales, hampering regional and global climate models. We reconstruct Saharan dust fluxes over Western Europe for the last 5000 years, by means of speleothem strontium isotope ratios (⁸⁷Sr/⁸⁶Sr) and karst modeling. The record reveals a long-term increase in Saharan dust flux, consistent with progressive North Africa aridification and strengthening of Northern Hemisphere latitudinal climatic gradients. On shorter, centennial to millennial scales, it shows broad variations in dust fluxes, in tune with North Atlantic ocean-atmosphere patterns and with monsoonal variability. Dust fluxes rapidly increase before (and peaks at) Late Holocene multidecadal- to century-scale cold climate events, including those around 4200, 2800, and 1500 years before present, suggesting the operation of previously unknown strong dust-climate negative feedbacks preceding these episodes.

Artificial and singular geochemical environments are created around the engineered barrier systems (EBS) designed to isolate high level nuclear wastes in deep geological repositories. A concrete-bentonite interface takes place within the EBS and it builds a significant chemical gradient (pH), approximately from pH 8 (bentonite) to pH 12 (low alkali concrete), in a few millimetre thickness. This disequilibrium triggers dissolution and precipitation reactions and form a thin altered region. In this area, poorly ordered authigenic clay minerals, mainly hydrated magnesium silicates, are formed adjacent to hydrated calcium silicates and calcite precipitates adhered to the interface with concrete. This paper presents the development of this authigenic mineral layer comparing 6–18 months to 13 years interfaces. Scanning Electron Microscopy with Energy Dispersive X-ray spectroscopy (SEM-EDX) morphological and chemical characterization with the aid of ternary plots, X-ray diffraction (XRD) and infrared (IR) data show the young to old interface evolution from single brucite layers to stevensite-saponite silicates composition. Geochemical calculations indicate that this layer acts as a pH~11 buffer useful to minimize bentonite alteration and to favour the retention of amphoteric metal ions.

Cementation using Ordinary Portland Cement (OPC) remains the standard method for conditioning low- and intermediate-level radioactive waste, including Spent Ion Exchange Resins (SIERs). This work presents an integrated strategy involving thermal pretreatment to minimize waste volume and eliminate organic constituents, followed by encapsulation within three distinct binders: CEM I, CEM III, and a novel one-part geopolymer. The one-part geopolymer system represents a significant operational innovation, enabling safe and simple “just-add-water” processing and avoiding the need to handle alkaline solutions. The proposed geopolymer, synthesized from metakaolin, blast furnace slag, and solid sodium silicate, was systematically benchmarked against conventional OPC matrices (CEM I, CEM III) by assessing their capacity to immobilize thermally treated SIER ashes under accelerated leaching conditions. For benchmarking, leaching indices for Cs and Sr were determined following the ANSI/ANS 16.9 standard protocol in three representative environments simulating operational and long-term repository scenarios, providing a quantitative evaluation of radionuclide retention and matrix durability. Results indicate that the one-part geopolymer improved leaching indices for Cs and Sr compared to both cementitious binders and complied with regulatory waste acceptance criteria. The comparative results highlight the potential of geopolymer technology to increase waste loading efficiencies and improve long-term safety, establishing a robust framework for future radioactive waste management approaches.