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Published bySophia Pitts Modified over 9 years ago
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By Prashant Selvaratnam Department of Earth Sciences University of Cambridge Supervisor: Dr. Ian Farnan
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Mineral Based Phosphate Ceramics Phosphate minerals: - Evidence from nature of long term stability. - Ability to incorporate tri- and tetra- valent actinides and other fission products. - Ability to incorporate halides. Ceramics: - High durability. - High waste loading. Oklo natural reactor, Gabon Image from DOE Office of Civilian Radioactive Waste Management.
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Fluorapatite Ca 10 (PO 4 ) 6 F 2 Structure and chemistry allow for a multitude of substitutions. Two distinct cationic sites: Four Ca1 sites, 9-fold co-ordination. Six Ca2 sites, 7-fold co-ordination. Suitable for waste streams from fluoride- salt extraction: Experimental pyroprocessing techniques. Decommissioning of nuclear weapons. Generation IV nuclear fuels.
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Fluorapatite Synthesis Solid state synthesis. 3Ca 3 (PO 4 ) 2 + CaF 2 Ca 10 (PO 4 ) 6 F 2 Mixture ground together. Sintered at 800 0 C for 2 hours. Re-ground and pressed into ~1g pellets. Calcinated at 1,000 0 C for 2 hours. Analysed by powder X-ray diffraction and 31 P Nuclear Magnetic Resonance. } X 2
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Powder X-ray Diffraction
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31 P NMR One Phosphorus environment. Peak at 2.3ppm. Full width half maximum ~1ppm.
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Ce Doping Ce used as a surrogate for Pu. Similar electronegativity, ionic radii and oxidation states. Require Ce 3+ state. Coupled substitution: Ce 3+ and Na + for 2Ca 2+ 3Ca 3 (PO 4 ) 6 + 10 x CeF 3 + (1-20 x )CaF 2 + 10 x NaF → (Ca (1-2 x ) Ce x Na x ) 10 (PO 4 ) 6 F 2 Where 0 ≤ x ≥ 0.05. Problems with melting samples. Reducing ramp rate from 20 0 C/min to 10 0 C/min helps.
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Ce Doping Use X-ray diffraction and NMR to study phase assemblages, solid solubility, Ce oxidation state and site distribution.
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SRIM Calculations Produce a sample with a uniform damage profile. Ions must completely penetrate sample. 29MeV/nucleon Pb ion beam, retarded to 11MeV/nucleon.
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Xenotime YPO 4 Empirical potential suitable for molecular dynamics simulations of radiation damage. Empirically tuned, using GULP, to re-produce: Inter-atomic distances and lattice parameters. Elastic constants. Mindful of phase separation into P 2 O 5 and Y 2 O 3. Interatomic potentials: Buckingham Potential: V(r) = Aexp(-Br) – C/r 6 Morse Potential: V(r) = D [1-exp(a(r-r o ))) 2 – 1] Where r is the inter-atomic distance.
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Xenotime Potentials Potential 1Potential 2*Potential 3 Charge balanced for P 2 O 5 & Y 2 O 3 X Y-O PotentialBuckingham O-O PotentialBuckingham P-O PotentialMorseBuckinghamMorse C11-0.4%+53%-5.9% C33+0.9%+12.9%+3.6% C44-6.1%+18.4%+3.0% C66+1.1%+52.9%+17.6% C12-47.2%+5.4%-40.0% C13+2.3%+16.3%-4.6% Lattice constant 10.0%-1.7%-0.2% Lattice constant 20.0%+3.3%+0.2% P-O distance0.0%+1.0%-12.0% Y-O distance 1+0.8%-7.0%+6.8% Y-O distance 2-1.7%+4.2%+4.0% * P-O-P bond angle term used
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Preliminary Conclusions Fluorapatite Pure phase fluorapatite synthesis possible via solid state methods. 31 P NMR peak at 2.3ppm. Problems with sample melting for Ce-doped sample synthesis in ambient atmosphere. Sample thickness of < 82µm required to obtain uniform damage profile in 11MeV/nucleon Pb beam. Xenotime Difficult to get a wholly satisfactory YPO 4 potential that is charge balanced with respect to P 2 O 5 and Y 2 O 3. Having a Morse potential between P and O improves the output.
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Future Work Fluorapatite Ce-doped sample synthesis under reducing atmosphere. NMR analysis of Ce-doped fluorapatite samples. Make and analyse 80µm thick, 1.5cm x 1.5cm samples for ion beam damage. Xenotime Do one GULP fit for YPO 4, P 2 O 5 and Y 2 O 3. Run DL_POLY radiation damage simulations using obtained potentials.
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Acknowledgements Ian Farnan, Martin Dove, Clive Brigden, Katie Gunderson, Tony Abraham, Martin Walker (University of Cambridge). Shirley Fong, Brian Metcalfe, Phillip Mallinson (AWE). Ram Devanathan (Pacific North West National Lab, US Department of Energy). Christina Trautmann, (GSI Helmholtz Centre for Heavy Ion Research) Lou Vance (Australian Nuclear Science and Technology Organisation).
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