This work investigates the potential of wollastonite-based brushite cement (WBC) for the stabilization and solidification of radioactive waste contaminated by 90Sr. This phosphate binder was formed by the reaction of wollastonite (CaSiO3) with a phosphoric acid solution containing borax and metallic cations (Al3+, Zn2+). Two cement pastes were investigated: a commercial binder (WBC-C) and an optimized formulation (WBC-O), produced using a zinc-free mixing solution with a higher aluminum content than that of WBC-C. Mineralogical characterizations using XRD, TGA, XRF, SEM-EDX, and Raman spectroscopy showed that both materials mainly contained amorphous hydrated silica and calcium aluminophosphate, along with crystalline brushite, residual wollastonite, and quartz. The stability of WBC-C under γ-irradiation was evaluated up to a dose of 1 MGy. The only observable effect was water radiolysis, leading to dihydrogen production at yields comparable to Portland cement matrices and geopolymers. Strontium leaching, assessed using the ANSI/ANS-16.1-2003 (R2008) procedure, followed a two-stage release mechanism combining surface wash-off and diffusion. The apparent diffusion coefficient Da of Sr in WBC-C was markedly lower than typical values reported for Portland cement matrices. WBC-O exhibited enhanced Sr retention, possibly due to its higher aluminum content, which refines mesopores and reduces diffusion pathways accessible to Sr. WBC binders therefore appear to be promising candidates for strontium immobilization.
28 August 2026 in Journal of the American Ceramic Society
This work investigates the potential of wollastonite-based brushite cement (WBC) for the stabilization and solidification of radioactive waste contaminated by 90Sr. This phosphate binder was formed by the reaction of wollastonite (CaSiO₃) with a phosphoric acid solution containing borax and metallic cations (Al3+, Zn2+). Two cement pastes were investigated: a commercial binder (WBC-C) and an optimized formulation (WBC-O), produced using a zinc-free mixing solution with a higher aluminum content than that of WBC-C. Both materials mainly contained amorphous hydrated silica and calcium aluminophosphate, along with crystalline brushite, residual wollastonite, and quartz. The stability of WBC-C under γ-irradiation was evaluated up to a dose of 1 MGy. The only observable effect was water radiolysis, leading to dihydrogen production at yields comparable to Portland cement matrices and geopolymers. Strontium leaching, assessed using the ANSI/ANS-16.1 procedure, followed a two-stage release mechanism combining surface wash-off and diffusion. The apparent diffusion coefficient Da of Sr in WBC-C was three orders of magnitude lower than typical values reported for Portland cement matrices. WBC-O showed enhanced Sr retention due to its higher aluminum content, which refines mesopores and reduces diffusion pathways accessible to Sr. WBC binders therefore appear to be promising candidates for strontium immobilization.
To achieve zero net carbon dioxide (CO2) emissions by 2050, the search for new alternative materials to replace Portland clinker is urgent. Biomass fly ash (BFA) is one of the possible materials. Given the extremely high variability in the mineralogical, chemical and microstructural properties of these ashes, a large number of samples must be explored. This study presents a physicochemical characterisation of wood and paper BFA, offering guidelines for sample preparation and data analysis. Four BFAs were characterised using particle size analysis, specific gravity, Brunauer–Emmett–Teller (BET)-surface area analysis, total carbon analysis, scanning electron microscopy, X-ray fluorescence, thermogravimetric analysis and X-ray diffraction (XRD). The studied biomass ashes were found to contain more than 15 phases, with 30 wt.% of potentially reactive phases, including both crystalline and amorphous components. The chemical composition of the amorphous phase is estimated to lie between that of calcareous fly ash and blast-furnace slag. The correlation between the XRD amorphous hump position and the calcium oxide/(silicon dioxide + aluminium oxide) (CaO/(SiO2+Al2O3)) ratio of the amorphous phase is further refined within the calcareous fly ash domain.