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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.
Yuezhou Wei, Tsuyoshi Arai, Harutaka Hoshi, Mikio Kumagai, Aimé Bruggeman, Patrick Goethals
Nuclear Technology | Volume 149 | Number 2 | February 2005 | Pages 217-231
Technical Paper | Reprocessing | doi.org/10.13182/NT05-A3591
Articles are hosted by Taylor and Francis Online.
We have studied a new aqueous reprocessing system that consists of anion exchange as the main separation method, electrolytic reduction for reducing U(VI) to U(IV), and extraction chromatography for minor actinide partitioning. In this work, hot tests were carried out on the main flow sheet (U and Pu recovery) using a nitric acid solution of a spent commercial boiling water reactor fuel with burnup of 55 000 MWd/t HM. First, a separation experiment was conducted using a column packed with AR-01 anion exchanger, and the separation behavior of about 20 elements was examined. Then electrolytic reduction was performed for the U(VI) eluate from the first column using a flow-type electrolysis cell. Subsequently, the reduced U solution was applied to the second AR-01 column to separate the U(IV) from contaminated fission products. Most amounts of Pu(IV)-Np(IV), were successfully separated and recovered in the first column. In the electrolysis, U(VI), Np(V,VI), and a trace amount of Pu(VI) were reduced to U(IV), Np(IV), and Pu(IV), respectively. In the second column, the U(IV) with small amounts of Np(IV) and Pu(IV) was completely separated from the fission products. These results demonstrated that the proposed U and Pu recovery process is essentially feasible, though more effective elution methods for Pd and Tc need to be investigated further.