The incorporation of Li2SO4 into barium borosilicate glass for nuclear waste immobilisation

• Published in: Journal of alloys and compounds 2022-03, Vol.897, p.162746, Article 162746
• Main Authors: Farzana, Rifat, Dayal, Pranesh, Karatchevtseva, Inna, Aly, Zaynab, Gregg, Daniel J.
• Format: Article
• Language: English
• Subjects: Barite; Barium; Barium oxides; Barium sulfate; Borosilicate glass; Crystallization; Depolymerization; Diffusion layers; Durability; Environmental assessment; Glass transition temperature; High temperature; Lithium Sulphate; Miscibility; Nuclear waste; Radioactive wastes; Raman spectroscopy; Sodium; Sodium sulfate; Sulfur; Sulfur trioxide; Sulphate incorporation; Wasteforms
• ISSN: 0925-8388; 1873-4669
• DOI: 10.1016/j.jallcom.2021.162746

•A glass wasteform was designed for Mo-99 production Li2SO4-rich wastes.•Incorporation of 2.78 wt% SO3 was achieved in the glass melted at 1200 °C.•At low temperature an immiscible layer of BaSO4 and Na2SO4 formed.•Formation of Na2SO4 lowered the sulphur incorporation rate compared of BaSO4.•PCT leach values showed satisfactory aqueous durability as glass wasteform. This study has systematically investigated the effect of Li2SO4 addition (2.75 −16.5 wt%) in barium borosilicate glass, to provide a pathway to optimise the glass composition and maximise sulphate incorporation. The work also provides a mechanistic understanding as to how SO42- is incorporated within the glass structure. The highest sulphate incorporation of 2.78 wt% SO3 (from 11 wt% Li2SO4 addition) was achieved without crystallisation following melting at 1200 °C. Sulphate incorporation in glass was confirmed by XRF, ICP, EDS and Raman analysis. Addition of Li2SO4 along with sodium and barium oxides improved the sulphate incorporation by mixed alkali network depolymerisation and the larger Ba cations helped to create sufficient space within the boron-silicate network to incorporate sulphate ions into the glass. An immiscible sulphate layer rich in BaSO4 and Na2SO4 formed on top of the glass at lower temperature (800–1100 °C) and subsequent diffusion of Na, Ba oxides and sulphur from this layer increased with increasing time and temperature to form a sulphate incorporated amorphous glass. Addition of Na2O played an important role to improve sulphate incorporation in the glass, as well as formation of an immiscible layer on top of the glass however, the formation of Na2SO4 lowered the sulphur incorporation rate at high temperature compared to BaSO4. Increasing the Li2SO4 content in the glass decreased the glass transition temperature. Aqueous durability testing using the standard PCT tests indicated the glass had satisfactory aqueous durability compared to benchmark environmental assessment glass. This study provides opportunities to convert Li+ and SO42- rich nuclear wastes into appropriate glass wasteforms.