Corrosion behavior of spent nuclear fuel in high pH solutions – Effect of hydrogen

2012 ◽  
Vol 1475 ◽  
Author(s):  
A. Loida ◽  
R. Gens ◽  
C. Bube ◽  
K. Lemmens ◽  
C. Cachoir ◽  
...  

ABSTRACTIn accordance with the Belgian “supercontainer design”, spent nuclear fuel (SNF) will be encapsulated in carbon steel canisters, surrounded by a concrete overpack for disposal in poorly-indurated clay. After re-saturation of the barriers by porewater, interactions with the concrete will result in solutions rich in NaOH, KOH and Ca(OH)2. Corrosion studies of SNF in ECW-type solution (Evolved Cement Water) and YCWCa-type solution (Young Cement Water with Ca) were performed under externally applied H2 overpressures over 426 days. Directly after H2 application, Tc concentrations decreased from >10-8 M to concentrations below detection limit. Based on the fractional release of selected fission products, low matrix dissolution rates of ~10-8/day were found in both experiments. U concentrations decreased finally to 1.5•10-9 M (YCWCa) and to 2.1•10-10 M (ECW), respectively. Am, Np and Pu concentrations were found throughout the experiments below their detection limits indicating an effective retention process.

2021 ◽  
Author(s):  
Xuesong Yan ◽  
Yaling Zhang ◽  
Yucui Gao ◽  
Lei Yang

Abstract To make the nuclear fuel cycle more economical and convenient, as well as prevent nuclear proliferation, the conceptual study of a simple high-temperature dry reprocessing of spent nuclear fuel (SNF) for a ceramic fast reactor is proposed in this paper. This simple high-temperature dry (HT-dry) reprocessing includes the Atomics International Reduction Oxidation (AIROX) process and purification method for rare-earth elements. After removing the part of fission products from SNF by a HT-dry reprocessing without fine separation, the remaining nuclides and some uranium are fabricated into fresh fuel which can be used back to the ceramic fast reactor. Based on the ceramic coolant fast reactor, we studied neutron physics of nuclear fuel cycle which consists operation of ceramic reactor, removing part of fission products from SNF and preparation of fresh fuels for many time. The parameters of the study include effective multiplication factor (Keff), beam density, and nuclide mass for different ways to remove the fission products from SNF. With the increase in burnup time, the trend of increasing 239Pu gradually slows down, and the trend of 235U gradually decreases and become balanced. For multiple removal of part of fission products in the nuclear fuel cycle, the higher the removal, the larger the initial Keff.


1999 ◽  
Vol 5 (S2) ◽  
pp. 848-849
Author(s):  
J.S. Luo ◽  
D.P. Abraham

Stainless steel-zirconium (SS-Zr) alloys have been developed as waste forms to immobilize and retain fission products generated during the electrometallurgical treatment of spent nuclear fuel. The baseline waste form is a stainless steel-15 wt.% zirconium (SS-15Zr) alloy, which is prepared by melting appropriate amount of Type 316 stainless steel (SS316) and high purity zirconium. As zirconium has very low solubility in iron, the addition of zirconium to SS316 results in the formation of ZrFe2 -type Laves intermetallic phases. The corrosion behavior of stainless steel has been widely studied; however, the corrosion behavior of the Zr-based-intermetallic has not been previously investigated. In this paper, we present a microstructural characterization of the corrosion layer formed on the Zr-intermetallic phase using energy-filtering transmission electron microscopy (TEM) and energy dispersive x-ray spectroscopy (EDS).Specimens of SS-15Zr alloy, crushed to 75 to 150 μm sizes, were immersed in 90°C deionized water for a period of two years.


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.


2004 ◽  
Vol 148 (3) ◽  
pp. 348-357 ◽  
Author(s):  
Yuichi Sano ◽  
Yoshihiko Shinoda ◽  
Masaki Ozawa

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>


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