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
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.