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Reprocessing. NUCP 2311 Radioactive waste Disposal and MAnagement. Reprocessing Concepts. Break down the spent nuclear fuel to separate the useful actinides (U, Pu, etc.) from the fission product and waste elements.
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Reprocessing NUCP 2311 Radioactive waste Disposal and MAnagement
Reprocessing Concepts • Break down the spent nuclear fuel to separate the useful actinides (U, Pu, etc.) from the fission product and waste elements. • Many actinides have half lives on the order of 100,000 to 1,000,000,000 years. • Contain useful energy content. • Most fission products have half lives on the order of 10, 50, 100, or 1000 years (exceptions include Tc-99 and a few others). • Some are useful for medical applications (e.g., Mo-99).
Highest Level Flowsheet U as U, UOx, or UF6 SNF Reprocessing Pu as nitrate, PuO2, or ? Spent Nuclear Fuel (metal or oxide) TRU (Waste?) Gaseous Waste (Kr, Xe, I, and Ru?) Fission Product HLW (Cs, Sr, Zr, Ni, La, . . .) Solid Waste (Cladding and other hardware) (LLW?) Process Chemistry
Reprocessed fuel wastes • Uranium- can be used as fuel • Plutonium- can be used as fuel • Other transuranics- waste stream • Waste Gasses- unknown, waste or vent to atmosphere • Fision products (Cs, Co, Sr)- Cs-Co can be used in irradiators(food or medical) Sr- can be used for electro- or thermal generators • Liquid waste- waste stream • Will be different forms of waste from original spent fuel but will be less volume
Processing Options • Aqueous Processing • Dissolve the spent fuel in acid. • Water-based acid solvents (e.g., HNO3) and water-insoluble organic solvents (e.g., Tributyl Phosphate - TBP) to extract and exchange the chemicals. • PUREX, UREX, THOREX, Bismuth Phosphate, and others. • Pyrochemical Processing • Molten Salts, “high” temperatures (~500ºC), and electrochemistry. • Uses electrons as the reducing agent! • Small-scale compact process.
General Fuel Cycle Operations Chopping/Decladding Physical Separations Chemical Pretreatment Spent Nuclear Fuel (metal or oxide) • Gas release • Powder/Particulate Control • Contamination Control • Gas release • Powder/Particulate Control • Contamination Control • Process Specific • Fuel type specific • Fission product release (more gas) • Chemistry, corrosion, and containment issues Product Treatment Storage forms or fuels for advanced burning Chemical Separations Waste Treatment Waste forms to storage or geologic repository • Process Specific • Fuel type specific • Fission product management (may have more gas) • Chemistry, corrosion, and containment issues • Element Distributions • Phase Separations Aqueous Processing Definitions Product = Effluent Waste = Raffinate
Chopping/Decladding • Some Design Questions • Do you remove the cladding before or after chopping? • How do you recover “all” of the fuel? • How do you define “all”? • What about fine particles? • What is the decontamination spec for the cladding? (is it LLW or HLW?) • Do you want/need to recover the fuel from the FCCI reaction zone? • FCCI = Fuel-Clad Chemical Interaction
Example: Roller-Straitener (Preliminary work in Japan/US, perhaps others . . . Not known to be planned for implementation) • Option designed to recover oxide powder. • Avoid acid dissolution. • Bend cladding and crush ceramic. • Single or multiple pass. • Must remove assembly hardware first. • Shake powder out after runs. • Technical Barriers • Radiation embrittlement concerns at high burnup. • Powder flowability concerns for oxide removal (agglomerates and bridging). • 100% recovery is a challenge (acid wash to get FCCI residue?)
Example: Chopping • Option designed to expose fuel for further processing. • Increase material surface area to enhance processing rates. • Simple chopping operation. • Multiple pins at a time. • Must remove assembly hardware first. • Shake powder out after runs. • Technical Issues to Manage (not barriers) • Possible dispersion of fine radioactive particles (esp. for oxide fuel). • Handling of liquid metal bond (Na, NaK or Pb-Bi) in advanced fuels.
Example: Voloxidation • Designed to convert UO2 to fluffy yellow powder • Scroll, pierce, or chop cladding to expose fuel • Heat in a flowing oxygen-rich environment (not 100% O2) • Density change causes swelling of fuel and rupture of cladding. • Powder ready for further treatment. • Rate controlled by temperature, surface area, and O2 feed rate.
Other decladding options that have been discussed • Direct Chlorination or Fluorination • Electrolysis: anodic dissolution of cladding into salt • Others are being investigated
Chemical Pretreatment • Highly process specific. • The chemical form of the “soup” is defined by the separation method selected. • Phase options: • Reaction Rate Speculation • = Prohibitively slow rates • ?= Potentially slow rates • = Reasonably fast rates • = Rapid reaction rates
Chemical Pretreatment: Aqueous • Dissolve collected fuel materials in nitric acid solution. • Precursor to liquid-liquid solvent extraction separations. • Accomplished by the manipulation of Pu and U valence state. • Rates and chemical species depend on the dissolver temperature. • Uranium Valence: • UO2 = U+4 (insoluble) • UO2(NO3)2 = U+6 (soluble)
a) b) Example: a) UO2 pellets and b) uranium metal electrochemically reduced from UO2 (ANL) Chemical Pretreatment: Pyrochemical • Molten salt processing • Halides: Cl-, F-,I-, and Br- • Molten Metal Solvents (historical) • Zn, Cd, Cu, Mg, alloys • Tend to focus on metallic and intermetallic chemistry. • Pretreatment by chemical or electrochemical reduction • Solubility is still a critical issue.
Question: How do you separate the Pu from the U? Answer: Chemistry Take advantage of the considerable differences in the rates of oxidation-reduction of the ions of Pu and U. Pu(IV) is much less stable and requires more powerful oxidants to form than either U(IV) or Np(IV). Pu(III) is more stable and easily formed by mild reducing agents than U(III) or Np(III). Np(V) is very stable. It is feasible to form situation containing: U(VI) as UO2+2 in aqueous solution Np(V) as NpO+ in aqueous solution Pu(III) or Pu(IV) in an insoluble inorganic complex Chemical Separations - Overview
Chemical Separations - Overview • Issue: Fission products with similar valence states in solution may (and do) follow Pu(III) and Pu(IV) into the organic phase? • Decontamination is possible through re-oxidizing to Pu(VI) and kicking it into a clean aqueous solution? • Based on these Ideas, a number of processing techniques have been designed and implemented. • Early work reviewed by J. Rydberg and L.G. Sillen, Acta Chem. Scand., v9 (1955) 1241-51.
Four Basic Separation Families • Co-Precipitation • Adjust solution chemistry to precipitate a solid Pu compound (salt) for Solid-Liquid separation. • Lanthanum Fluoride Cycle, Bismuth Phosphate (BiPO4) Cycle, and Double Sulphate Precipitation. • Solvent Extraction • Selective extraction of Pu from an aqueous solution into an immiscible organic liquid. • REDOX, PUREX, Chelation, BUTEX, TLA (tertiary amines), and many more. • Modern methods are PUREX and portions of UREX. • Note: PUREX and UREX do not normally use reduction-oxidation reactions. • Non-Aqueous Methods • Separation through inorganic chemistry. • Molten metals, molten salts, pyrometallurgicalslagging, fluoride volatility, electrometallurgical processing, and combinations of all of the above. • Ion Exchange Separation • Selective cation exchange for Solid-Liquid extraction. • Often used for higher actinide separations (e.g., Am and Cm)
Bismuth Phosphate/Lanthanum Fluoride Carrier Precipitation • Used from 1945 to ? to produce plutonium. • Precipitates Pu metal leaving U in solution with the fission products. • Fission products removed in a subsequent cycle. • Lack the ability to extract uranium.
Pu production • Lanthanum Fluoride Process • Start with uranyl nitrate solution containing Pu and FPs from dissolver. • Speciation: Pu(IV), Np(V), and U(VI). • Results: • Solid LaF3 with most of the fission products. • Liquid with nearly pure PuO2+2 • Bismuth Phosphate Process • Start with uranyl nitrate solution containing Pu and FPs from dissolver • Speciation: Pu(IV), Np(V), and U(VI). • Results • BiPO4 is very selective of Pu and insoluble in HNO3. • Direct precipitation of PuO2
Solvent Extraction • Aqueous solution of a metallic component is brought into equilibrium with an immiscible organic solvent for the component • The two phases are separated • The component will be found distributed between the two phases • Characterized by the distribution coefficient
From: Joseph J. Katz, Glen T. Seaborg, and Lester R. Morss, “The Chemistry of the Actinide Elements, Second Edition,” Volume 1, p. 519 (Chapman and Hall, 1986).