1 / 39

Modelling and theory of systems relevant to nuclear waste processing Kostya Trachenko

Modelling and theory of systems relevant to nuclear waste processing Kostya Trachenko Queen Mary University of London. Today’s talk Molecular dynamics of radiation damage in waste forms. My research interests:

rdacus
Download Presentation

Modelling and theory of systems relevant to nuclear waste processing Kostya Trachenko

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Modelling and theory of systems relevant to nuclear waste processing Kostya Trachenko Queen Mary University of London

  2. Today’s talk Molecular dynamics of radiation damage in waste forms My research interests: - Theory (dynamics and thermodynamics) of liquids, liquid-glass transition and supercritical stateExtension to field theory and cosmology- Modelling radiation damage effects (nuclear and fusion applications)

  3. Transport and diffusion in radiation-damaged zircon • Resistance of materials to amorphization by radiation damage • Properties of collision cascades • High-energy radiation damage in iron • Diffusion rates and activation energies in radiation-amorphized zirconolite

  4. Modelling of high-energy radiation damage Future of nuclear industry is linked to safe encapsulation of nuclear waste • Radiation damage in materials to be used to encapsulate highly radioactive nuclear waste: ceramic materials 2. Radiation damage in nuclear fuels in current and future nuclear reactors: metals 3. Radiation damage in future fusion reactors: metals

  5. Crystalline ceramics as waste forms • Safe and more durable alternative to glasses: CaTiO3, CaZrTi2O7, BaAl2Ti6O16 and TiO2- geochemically stable minerals which have immobilised uranium and thorium for billions of years. Can incorporate high-level radioactive waste (Pu, Sr, Ba, Cs) • Pyrochlore (Gd, Sm, Hf-based)-rich titanate phases for Pu encapsulation: high waste load plus criticality control (neutron absorbants) • Other potential “waste forms”: ZrSiO4, ZrO2, Gd2Zr2O7 and so on What are the effects of radiation damage? How do they affect performance of waste forms?

  6. Effect of radiation-induced amorphization on diffusion What are long-term (millions of years) effects of irradiation on the performance of waste forms? Case study: zircon ZrSiO4 minerals are ~1 billion years old, completely amorphous yet intact Absorbs large ions like Pu on Zr site Can we learn from Nature?

  7. What are the effects of radiation damage? Processes are too fast and collision cascades are too small for experiments -> MD simulations Challenge of large energy and large size: Recoil energies: 100-500 keV Require very large MD boxes Not achievable previously

  8. Molecular dynamics simulation of radiation damage: challenge of large energy and large size Details: 1. Empirical potentials; short-range ZBLpotential at short <~1 Å distances 2. Perfectly scalable MD code based on domain decomposition strategy (DL_POLY MD package) 3. Parallel computers (Cambridge HPC, HPCx, HECToR, Archer) 4. Adapted MD code to handle out-of-equilibrium conditions (variable time step, boundary scaling)

  9. High-energy U recoils in ZrSiO4 50 keV U recoil and their overlap Density variations appeared inside cascades and during their overlap Density variations later confirmed in diffuse X-ray scattering

  10. The value of percolation threshold in the continuum percolation is pc=0.3 (approx.) (non-trivial because it is continuous percolation) This gives channels of increased diffusion and explains percolation-type increases of transport (Geisler et al, Trachenko et al, 2003, 2004)

  11. Amorphizability A material is amorphizable if it is able to form a covalent network

  12. Resistant vs amorphizable materials Some materials are easily amorphized (silicates and titanates) Others are extremely resistant to amorphization (e.g., ZrO2, Gd2Zr2O7) What is the nature of the process of resistance to amorphization by radiation damage? The same question is relevant in other areas: GaN and ZnO are considerably more resistant than GaAs, GaSb, Si etc

  13. Understanding resistance to amorphization to radiation damage Resistance is governed by activation barriers for damage recovery and the nature of the bond

  14. Understanding resistance to amorphization • Many criteria do not generally work (review in JPCM 2004) • Out of ~10 criteria, Naguib&Kelly (1975) empirically noticed that for binaries, resistance increases with ionicity (Pauling ionicity scale). Many other followed. • Need: generality and applicability to all systems =>physical explanation • Way to quantify: need hard numbers. Neither Pauling nor Phillips scales work generally! Trachenko et al, PRB 2005

  15. Understanding resistance to amorphization Trachenko et al, PRB 2005 Prediction, verified experimentally Review paper in JPCM 2004: 115 complex materials with no exception to this rule: increased covalency (reduced ionicity) decreases resistance

  16. Molecular dynamics: look at the process in detail Rutile TiO2

  17. Two types of damage relaxation: 1. Elastic reversible relaxation of crystalline lattice around the swollen cascade – large peak in Ndef 2. Irreversible topological damage 1-2 ps 50-100 ps

  18. Resistance to amorphization 50 keV U recoil Poor recovery Good and perfect recovery Intermediate recovery GeO2 TiO2 MgO Al2O3 SiO2 t=1 ps t=5, 50 ps MD simulations reproduce experimental behaviour of resistance to amorphization. Damage increases with the stiffness of O-O interaction

  19. Why do empirical potentials reproduce activation barriers that govern damage recovery?

  20. Resistance to amorphization • Classical MD simulations reproduce experimental behaviour of resistance to amorphization • MD simulations can be used to predicthighly resistant materialswhere resistance to amorphization operates on the time scale of picoseconds. Successfully predicted resistance of series of pyrochlores. • Slower recovery processes are possible. Even then, predictions work if recovery is slow (cascade size in MD simulations on ps time scale=in billion-year-old samples from NMR experiments)

  21. Radiation damage in iron Simulate radiation damage in fusion reactors: ~1 Mev Fe recoil atoms from 14 MeV neutrons Also relevant for nuclear fuels: fission products (many MeVs)These energies were not studied before, yet are important to simulate Need up to 1 billion atoms in a MD box. The size of this system is about 0.2 micrometers – size where, for the first time, simulations and many experiments meet!

  22. DL_POLY development work (supported by the EPSRC grant) Radiation damage-specific developments: • Identification of radiation damage and defects • Electronic energy loss mechanism (friction term and two-temperature models) • Tuning potentials to very non-equilibrium conditions

  23. DL_POLY development work(supported by the current EPSRC grant) General developments related to very large system sizes: • Calculation of properties on the fly (one configuration of 250 mln atoms is about 100 Gb, 10,000-frame history file is Petabyte in size) • Change the paradigm of how to run&analyze MD results – MD of the future • Relevant for many interested in phenomena operating on microscale: shock, fracture, initiation of micro-cracks, micro-structural changes, interfacial effects, macromolecules, biological systems and so on

  24. 0.2 - 0.5 MeV Fe recoils in iron • These energies have not been simulated before • Many-body (embedded atom) potential optimized against several defect energies in alpha-iron • 100-500 million atoms, system size ~100-200 nm • 24,000-60,000 parallel HeCTOR processors • Great PhD student! 1. What does the collision cascade actually look like?First visualization of high-energy cascades 2. Novel insights into the cascade structure:continuous damage morphology vs sub-cascade branching

  25. 0.5 MeV recoils in Fe Displaced atoms Defect atoms

  26. 0.5 MeV recoils in Fe Displaced atoms Defect atoms

  27. 500 keV Fe recoils in iron anharmonicity displaced atoms defect atoms Look at defects locally: Large (~100 atoms) clusters of interstitials and vacancies. Quantify and discuss their stability. News Story in JPCM 2013

  28. Current work: Radiation damage at interfaces and effects of microstructure Gd2Zr2O7, Gd2Zr2O7 and CaZrTi2O7 interface

  29. Current work: Radiation damage at interfaces and effects of microstructure Slab: defects Spherical inclusion: defects • The number of displaced and defect atoms increases compared to the crystal • Presumably due to disorder at interfaces and grains

  30. Current work: interfaces in Y2O3-ZrO2 5% Y 0% Y 10% Y 8% Y 11% Y 15% Y 20% Y 12% Y Cubic phase Orthorhombic (not monoclinic) phase

  31. Current work: effect of shock waves Can the damage due to shock waves be PERMANENT?

  32. Diffusion in waste forms What are the effects of amorphization and density decrease on diffusion? • Problem of long time scales • Several methods exist (search for transition states, temperature-accelerated dynamics and so on) • We simulate at high temperature and extract activation energy barriers

  33. Solid-state diffusion in amorphous zirconolite ZrCaTi2O7 • Under typical waste load, zirconolite becomes amorphousin about 1000 years • Most of radiation damage will take place in an amorphous system • Insert some U atoms. Prepare an amorphous structure by liquid quenching • Directly observe diffusion of atomic species • Calculate diffusion coefficient D from <r2>=6Dt at different temperature and density and calculate activation energy barrier U from D=D0exp(-U/T) • Disentangle effects of amorphization and density on diffusion(not possible in the experiment) • Yang et al, Journal of Applied Physics 2014

  34. Diffusion of O atoms Disorder increases diffusion of O atoms Density does not

  35. Diffusion of cations Smaller density increasesdiffusion of cations

  36. Activation energy barriers O Ca • Activation energies for cations dramatically depend on disorder (no diffusion is seen in the crystal) butnot on density – a surprise. • Activation energies of O atoms are not sensitiveto disorder and density • Diffusion pre-factors increase at smaller density forcations by 1.5-3. • Diffusion pre-factors for O do not depend ondensity and increase as a result of amorphization • not affected by density – a surp Zr Ti U

  37. Activation energies and pre-factors enable us to predict diffusion of atomic species at long times and evaluate performance of a nuclear waste

  38. Thank you

More Related