The Effects of Uranium on the Structure of Iron Phosphate Glasses

1999 ◽  
Vol 556 ◽  
Author(s):  
Yaspal Badyal ◽  
Mevlut Karabulut ◽  
Kanishka Marasinghe ◽  
Marie-Louise Saboungi ◽  
Dean Haeffner ◽  
...  

AbstractBecause of their high chemical durability and waste loading capacity, iron phosphate glasses are a natural candidate for a nuclear waste disposal medium. We have studied the effects of uranium on the structure of iron phosphate glasses with both neutron and high-energy x-raydiffraction. The results of neutron scattering, which is mostly sensitive to pair correlations involving light atoms i.e. O-O, Fe-O and P-O, indicate the main structural features of the base glass are largely unaffected by the addition of UO2. The nearest-neighborbour P-O, Fe-O and O- O peaks remain at the same position in real space and their intensities scale approximately with concentration. These findings are consistent with earlier results using Raman scattering and EXAFS on the Fe-K edge, where in both cases the spectra remain similar to the base glass. The results of high-energy x-ray scattering, which is sensitive to correlations involving the heavier atoms and thus complements the neutron measurements, are also consistent with the overall picture of uranium occupying interstitial sites in the relatively undisturbed base glass structure. Combining the neutron and x-ray data for a 10 mol% UO2 glass suggests the intriguing possibility of a U6+ uranyl ion configuration although further work is needed to establish the precise local structure and valence state of uranium in these glasses.

2003 ◽  
Vol 15 (36) ◽  
pp. 6143-6153 ◽  
Author(s):  
U Hoppe ◽  
M Karabulut ◽  
E Metwalli ◽  
R K Brow ◽  
P J v ri

2000 ◽  
Vol 87 (5) ◽  
pp. 2185-2193 ◽  
Author(s):  
M. Karabulut ◽  
G. K. Marasinghe ◽  
C. S. Ray ◽  
G. D. Waddill ◽  
D. E. Day ◽  
...  

1999 ◽  
Vol 14 (6) ◽  
pp. 2628-2639 ◽  
Author(s):  
C. H. Booth ◽  
P. G. Allen ◽  
J. J. Bucher ◽  
N. M. Edelstein ◽  
D. K. Shuh ◽  
...  

Fe K-edge x-ray absorption fine-structure (XAFS) measurements were performed on glass samples of (Fe3O4)0.3(P2O5)0.7 with various amounts of Na2O or UO2. Near-edge and extended XAFS regions are studied and comparisons are made to several reference compounds. We find that iron in the base glass is ∼25% divalent and that the Fe2+ coordination is predominantly octahedral, while Fe3+ sites are roughly split between tetrahedral and octahedral coordinations. Also, we measure roughly one Fe–O–P link per iron. Substitution of Na2O or UO2 up to 15 mol% primarily affects the first Fe–O shell. The results are compared to data from the related material Fe3(P2O7)2.


2009 ◽  
Vol 355 (31-33) ◽  
pp. 1571-1573 ◽  
Author(s):  
M. Karabulut ◽  
M. Yuksek ◽  
G.K. Marasinghe ◽  
D.E. Day

2008 ◽  
Vol 354 (52-54) ◽  
pp. 5542-5546 ◽  
Author(s):  
Dong Qiu ◽  
Robert M. Moss ◽  
Dave M. Pickup ◽  
Ifty Ahmed ◽  
Jonathan C. Knowles ◽  
...  

2002 ◽  
Vol 304 (1-3) ◽  
pp. 188-194 ◽  
Author(s):  
S.T. Reis ◽  
D.L.A. Faria ◽  
J.R. Martinelli ◽  
W.M. Pontuschka ◽  
D.E. Day ◽  
...  

1999 ◽  
Vol 249 (2-3) ◽  
pp. 106-116 ◽  
Author(s):  
M Karabulut ◽  
G.K Marasinghe ◽  
C.S Ray ◽  
D.E Day ◽  
O Ozturk ◽  
...  

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