KNa3(UO2)2(Si4O10)2(H2O)(4), a new compound formed during vapor hydration of an actinide-bearing borosilicate waste glass

Citation
Pc. Burns et al., KNa3(UO2)2(Si4O10)2(H2O)(4), a new compound formed during vapor hydration of an actinide-bearing borosilicate waste glass, J NUCL MAT, 278(2-3), 2000, pp. 290-300
Citations number
18
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Nuclear Emgineering
Journal title
JOURNAL OF NUCLEAR MATERIALS
ISSN journal
00223115 → ACNP
Volume
278
Issue
2-3
Year of publication
2000
Pages
290 - 300
Database
ISI
SICI code
0022-3115(200004)278:2-3<290:KANCFD>2.0.ZU;2-O
Abstract
Vapor hydration experiments on a U-doped borosilicate waste glass at 200 de grees C produced a novel uranium silicate. Single crystal X-ray structure a nalysis of this phase indicate the ideal formula KNa3(UO2)(2)(Si4O10)(2)(H2 O)(4), although the compound shows some compositional variability. It is mo noclinic, space group C2, Z = 2, a = 1.2782(1), b = 1.3654(1), c = 0.82677( 8) nm, beta = 119.240(1)degrees. The structure was solved by direct methods and refined to an agreement index (R) of 3.6% for 2239 unique observed (\F -0\ greater than or equal to 4 sigma(F)) reflections and a goodness-of-fit of 1.05. The structure contains vertex-sharing silicate tetrahedra arranged in four and eight-membered rings that are linked to give sheets parallel t o (0 0 1). The sheets are cross-linked by vertex-sharing with UrO(4) square bipyramids [Ur = (UO2)(2+) uranyl ion], forming a framework of polyhedra o f higher bond-valence. The title phase is the major sink for U during glass corrosion at 200 degrees C after approximately 60 days in a saturated vapo r environment. Consideration of the structural sites reveals the potential of this compound to incorporate radionuclides from a variety of nuclear-was te glasses over a wide range of environmental conditions. (C) 2000 Elsevier Science B.V. All rights reserved.