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Ion-Exchange Properties of Microporous Tungstates

Christopher S. GriffithAustralian Nuclear Science and Technology Organization, PMB 1, Menai, NSW 2234, AustraliaVittorio LucaAustralian Nuclear Science and Technology Organization, PMB 1, Menai, NSW 2234, Australia
2004de
ABI

Abstract

Hydrothermally prepared microporous, hexagonal tungsten bronze (HTB) phases display promising distribution coefficients (Kd) for both Cs+ (2−100 ppm) and Sr2+ (0.5−60 ppm) cations in acidic (1.0 M HNO3) radioactive waste (radwaste) simulants. The selectivity for Cs+ and Sr2+ increases significantly on isomorphous substitution of molybdenum into the tungstate framework and is optimal for material of composition Na0.2Mo0.03W0.97O3·ZH2O. This composition results from attempts to prepare materials doped at a 10 atom % level viz. Na0.2Mo0.1W0.9O3·ZH2O (Mo0.1−HTB). Both the parent HTB and Mo0.1−HTB phases reach maximum uptake of Cs+ and Sr2+ after 30−60 min contact. The cation exchange capacity (CEC) of the parent HTB phase for Cs+ and Sr2+ is ca. 0.2 mmol·g-1 (26.6 g·kg-1) and 0.12 mmol·g-1 (10.5 g·kg-1), respectively, with a 100% increase displayed on 0.03 atom % molybdenum incorporation into the tungstate framework. The optimized Mo0.1−HTB sorbent displays good tolerance of the alkali metal cations, Na+, K+, and Ca2+, with respect to the sorption of Cs+ from acidic solutions. In contrast, the sorption of Sr2+ from similar solutions is reduced to a much greater extent by the presence of these cations.

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