scholarly journals Depleted Uranium Oxides and Silicates as Spent Nuclear Fuel Waste Package Fill Materials

1996 ◽  
Vol 465 ◽  
Author(s):  
C. W. Forsberg

ABSTRACTA new repository waste package (WP) concept for spent nuclear fuel (SNF) is being investigated. The WP uses depleted uranium (DU) to improve performance and reduce the uncertainties of geological disposal of SNF. The WP would be loaded with SNF. Void spaces would then be filled with DU (∼0.2 wt % 235U) dioxide (UO2) or DU silicate-glass beads.Fission products and actinides can not escape the SNF UO2 crystals until the UO2 dissolves or is transformed into other chemical species. After WP failure, the DU fill material slows dissolution by three mechanisms: (1) saturation of WP groundwater with DU and suppression of SNF dissolution, (2) maintenance of chemically reducing conditions in the WP that minimize SNF solubility by sacrificial oxidation of DU from the +4 valence state, and (3) evolution of DU to lower-density hydrated uranium silicates. The fill expansion minimizes water flow in the degraded WP. The DU also isotopically exchanges with SNF uranium as the SNF degrades to reduce long-term nuclear-criticality concerns.

1998 ◽  
Vol 121 (2) ◽  
pp. 174-188 ◽  
Author(s):  
Bernd Grambow ◽  
Andreas Loida ◽  
Emmanuel Smailos

Author(s):  
Jerzy Narbutt

<p>Recycling of actinides from spent nuclear fuel by their selective separation followed by transmutation in fast reactors will optimize the use of natural uranium resources and minimize the long-term hazard from high-level nuclear waste. This paper describes solvent extraction processes recently developed, aimed at the separation of americium from lanthanide fission products as well as from curium present in the waste. Depicted are novel poly-N-heterocyclic ligands used as selective extractants of actinide ions from nitric acid solutions or as actinide-selective hydrophilic stripping agents.</p>


2021 ◽  
Vol 1 ◽  
pp. 237-238
Author(s):  
Michel Herm ◽  
Elke Bohnert ◽  
Luis Iglesias Pérez ◽  
Tobias König ◽  
Volker Metz ◽  
...  

Abstract. Disposal of spent nuclear fuel (SNF) in deep geological repositories is considered a preferential option for the management of such wastes in many countries with nuclear power plants. With the aim to permanently and safely isolate the radionuclide inventory from the biosphere for a sufficient time, a multibarrier system consisting of technical, geotechnical and geological barriers is interposed between the emplaced waste and the environment. In safety assessments for deep underground repositories, access of water, followed by failure of canisters and finally loss of the cladding integrity is considered in the long-term. Hence, evaluating the performance of SNF in deep geological disposal systems requires process understanding of SNF dissolution and rates as well as quantification of radionuclides release from SNF under reducing conditions of a breached container. In order to derive a radionuclide source term, the SNF dissolution and alteration processes can be assigned to two steps: (i) instantaneous release of radionuclides upon cladding failure from gap and grain boundaries and (ii) a long-term release that results from dissolution of the fuel grains itself (Ewing, 2015). In this context, research at KIT-INE has focused for more than 20 years on the behavior of SNF (irradiated UO2 and MOX fuels) under geochemical conditions (pH, redox and ionic strength) representative of various repository concepts, including the interaction of SNF with backfill material, such as bentonite as well as the influence of iron corrosion products, e.g. magnetite and radiolytic reactions on SNF dissolution mechanisms. Since 2001, KIT-INE has contributed with experimental and theoretical studies on the behavior of SNF under repository relevant conditions to six Euratom projects viz SFS (2001–2004), NF-PRO (2004–2006), MICADO (2006–2009), RECOSY (2007–2011), FIRST-Nuclides (2012–2014) and DISCO (2016–2021). Moreover, since 2007, overall 4 consecutive projects for the Belgian waste management organization, ONDRAF-NIRAS, were performed on the behavior of SNF under conditions representative of the Belgian “Supercontainer” concept. In this contribution, we summarize major achievements of theses research projects to understand and quantify the radionuclide release from dissolving SNF under repository conditions. In particular, the dependence of radionuclide release on the chemical composition of the aqueous and gaseous phase in the proximity of repositories in different types of host rock is discussed.


2002 ◽  
Vol 757 ◽  
Author(s):  
Charles W. Forsberg ◽  
Leslie R. Dole

ABSTRACTMost fission products and actinides in spent nuclear fuel (SNF) are trapped in the uranium dioxide (UO2) crystal structure and cannot escape until the UO2 is oxidized. Oxidation destroys the crystal structure, exposes the radionuclides to groundwater, and creates the potential for dissolution. For a repository in an oxidizing geochemical environment, the potential exists to delay the release of radionuclides for hundreds of thousands to millions of years by using a combination of excess depleted uranium dioxide and iron in the waste package (WP) to locally maintain chemically reducing conditions. This approach limits the rate of oxygen transport to the SNF after WP failure. Alternative methods of oxygen transport to the SNF were investigated, including transport by groundwater, diffusion through air, and diffusion through water.


2002 ◽  
Vol 713 ◽  
Author(s):  
Charles W. Forsberg ◽  
Leslie R. Dole

ABSTRACTDepleted uranium dioxide (DUO2) waste packages (WPs) for disposal of spent nuclear fuel (SNF) are being investigated to (1) reduce radionuclide releases from WPs, (2) decrease the potential for repository nuclear criticality events, (3) provide radiation shielding, and (4) provide a means to beneficially use excess depleted uranium (DU). The DUO2 is incorporated into the WP as (1) a particulate fill for void spaces within the package and (2) a component of a DUO2-steel cermet (DUO2 embedded in steel) that replaces the steel components of the WP. Depending upon the design, there is 3 to 8 times as much DUO2 as SNF UO2 in the WP. Most radionuclides in the SNF cannot be released until the UO2 crystal structure is destroyed. The DUO2 surrounding the SNF slows the degradation of the SNF UO2 in the interior. This behavior is similar to the mechanisms that slow the degradation of natural uranium ore bodies containing UO2. The results of initial investigations and the expected thermodynamic WP behavior are described.


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