The Fe–O coordination in iron phosphate glasses by x-ray diffraction with high energy photons

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


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

2005 ◽  
Vol 60 (7) ◽  
pp. 517-526 ◽  
Author(s):  
Uwe Hoppe ◽  
Yanko Dimitriev ◽  
Pal Jóvári

X-Ray diffraction, using high-energy photons from a synchrotron, was used to extend the investigation of (ZnO)x(P2O5)1−x glasses to samples of ZnO content close to x = 0.8 which were obtained by roller-quenching. The isolated PO4 tetrahedra are surrounded by ZnOn polyhedra, where Zn−O coordination numbers of ∼ 4.5 are determined. The small increase of NZnO from ∼ 4 at metaphosphate composition (x = 0.5) to ∼ 4.5 is not sufficient to explain the strong increase of the packing density beyond the minimum at x = 0.5. The medium-range order was analyzed on the basis of partial SPP(Q) and SZnZn(Q) factors obtained from Reverse Monte Carlo simulations of glasses with 0 ≤ x ≤ 0.8. The positions of the first peaks in these factors, the number densities of P and Zn atoms and knowledge of definite P-P and Zn-Zn distances were used to check the applicability of simple models such as the dense packing of uniform P- and Zn-centered spherical environments for glasses with x=0.8 and 0.5, the packing of corrugated sheets for vitreous P2O5 and the packing of phosphate chains for Zn metaphosphate glass.


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

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

2002 ◽  
Vol 297 (2-3) ◽  
pp. 263-274 ◽  
Author(s):  
Uwe Hoppe ◽  
EzzEldin Metwalli ◽  
Richard K Brow ◽  
Jörg Neuefeind

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