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Colin Judge: Testing structural materials in Idaho’s newest hot cell facility
Idaho National Laboratory’s newest facility—the Sample Preparation Laboratory (SPL)—sits across the road from the Hot Fuel Examination Facility (HFEF), which started operating in 1975. SPL will host the first new hot cells at INL’s Materials and Fuels Complex (MFC) in 50 years, giving INL researchers and partners new flexibility to test the structural properties of irradiated materials fresh from the Advanced Test Reactor (ATR) or from a partner’s facility.
Materials meant to withstand extreme conditions in fission or fusion power plants must be tested under similar conditions and pushed past their breaking points so performance and limitations can be understood and improved. Once irradiated, materials samples can be cut down to size in SPL and packaged for testing in other facilities at INL or other national laboratories, commercial labs, or universities. But they can also be subjected to extreme thermal or corrosive conditions and mechanical testing right in SPL, explains Colin Judge, who, as INL’s division director for nuclear materials performance, oversees SPL and other facilities at the MFC.
SPL won’t go “hot” until January 2026, but Judge spoke with NN staff writer Susan Gallier about its capabilities as his team was moving instruments into the new facility.
Masatoshi Iizuka, Masaaki Akagi, Takashi Omori
Nuclear Technology | Volume 181 | Number 3 | March 2013 | Pages 507-525
Technical Papers | Reprocessing | doi.org/10.13182/NT13-A15807
Articles are hosted by Taylor and Francis Online.
A new treatment process was proposed for the anode residue from a molten salt electrorefining step in the pyrometallurgical reprocessing of spent metallic fast reactor fuel. This treatment process consists of two steps: (a) oxidation of the remaining actinides in the anode residue by the addition of CdCl2 and (b) removal of the accompanying chloride by high-temperature distillation. The oxidation of the remaining uranium by CdCl2 was studied using anode residue from previous electrorefining experiments using U-Zr alloys. The reaction between uranium and CdCl2 was completed in [approximately]2 days with a satisfactory chlorine balance among the species in the molten chlorides solvent. A high uranium oxidation rate was attained by appropriately controlling the rate of CdCl2 addition. The high-temperature distillation tests were carried out at 1473 K with pressure of [approximately]300 Pa to remove the solvent accompanying the anode residue. The chloride content in the anode residue was lowered to 1% to 2.5% by the distillation operation. Although the anode residue was heated to 1673 to 1773 K at a pressure of [approximately]50 kPa after the distillation, it was not melted completely. The remaining ratio of uranium after the electrorefining and the above treatment process was evaluated to be 0.04% to 0.20%. Material flow calculations were performed for a pyrometallurgical reprocessing facility equipped with the anode residue treatment process. It showed that (a) the chlorine and uranium supply/demand balance is maintained unless the remaining ratio of uranium after electrorefining exceeds a certain value and (b) the addition of the anode residue treatment process does not have an adverse effect on either the performance of the overall process or the facility design.