Leaching behaviour of cementitious nuclear wasteforms containing caesium and strontium

The leaching behaviour and physicochemical properties of cementitious nuclear wasteforms containing caesium and strontium waste simulants has been investigated. The cement wasteform consisted of a 9∶1 blend of blast furnace slag and ordinary Portland cement. Both non-loaded samples and samples that were waste loaded with 3 wt-% caesium and strontium added as nitrates have been studied. The cement hydration phases in the samples were identified, and the porosity and microstructure were analysed before leaching. The samples were leached for up to 6 months and the leached elements quantified. In the waste loaded cements, portlandite was not formed, and the monosulphate AFm phase appeared to be altered by the incorporation of the Sr(NO3)2. Incorporation of Cs and Sr also resulted in the increase in the leach rate of Ca2+

Phosphate modification of calcium aluminate cement to enhance stability for immobilisation of metallic wastes

Cementing systems based on calcium aluminate cement (CAC) have been studied as an alternative cement matrix for the encapsulation of intermediate level wastes (ILWs) arising from the nuclear industry. Calcium aluminate cement based systems have great potential for the incorporation of aluminium containing ILW owing to the near neutral internal pH of these binders. However, CAC based binders usually undergo phase conversion from the metastable hydration phases C3AH6 and/or C2AH8 to the stable C3AH6, resulting in strength regression and dimensional instability. The present study investigates the feasibility of CAC modification to prevent this detrimental process of phase conversion. Two different types of sodium phosphates are used to modify a CAC system, and the setting behaviour and the mineralogy of the binder products were studied. It is shown that it is possible to avoid the conventional phase conversion of CAC hydrates due to the formation of an amorphous aluminate phase in place of the metastable hydrates, leading to the production of a phase assemblage, which is stable for at least 180 days

Probing the water phases and microstructure in a model cement blend matrix used for the encapsulation of intermediate level nuclear wastes

The changes in microstructure and content of water phases during hydration of a 3:1 BFS:OPC blend are investigated by Mercury Intrusion Porosimetry (MIP), freeze-drying, Thermal Gravimetric Analysis (TGA) and 1H Nuclear Magnetic Resonance (NMR) relaxometry. MIP indicates that during the blend hydration, a reduction in the population of capillary pores (larger than about 100 nm) occurs while the population of gel pores (smaller than few tens of nanometres) increases. Between 3 and 90 days, the porosity estimated by MIP decreases from about 36% down to 18% while the median pore size decreases from about 140 nm down to 6 nm. 1HNMR relaxometry shows that after 1 day of hydration, nearly 70% of the evaporable water is held in capillary pores while about 30% is present in gel pores. After two weeks, most of the evaporable water (90%) is found in pores smaller than few tens of nanometres. : The amount of evaporable water detected by freeze drying decreases from less than 20 wt.% after one week of hydration down to about 16.3 wt.% after 90 days while the amount of chemical ly bound water related to the degree of advancement of the cement hydration and detected by TGA increases from 8 wt.% to 10.3 wt.%. During hydration the BFS:OPC blend matrix evolves from an open microporous network to one of a poorly connected network of water rich nanopores with increasing amounts of chemically bound water. © 2006 Materials Research Society