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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.
Noriyuki Momoshima, Yusaku Nagao, Takahiro Toyoshima
Fusion Science and Technology | Volume 48 | Number 1 | July-August 2005 | Pages 520-523
Technical Paper | Tritium Science and Technology - Containment, Safety, and Environment | doi.org/10.13182/FST05-A980
Articles are hosted by Taylor and Francis Online.
We evaluated electrolytic separation factors of hydrogen isotopes by SPE (Solid Polymer Electrolyte) for application to environmental tritium analysis. The apparent separation factors a for deuterium and a for tritium were determined as 3.5 ± 0.1 and 6.2 ± 0.5, respectively. The tritium enrichment of 8.4 times was achieved, when a 1000 ml of sample water was electrolyzed to about 60 ml. The chemical composition changes before and after the electrolysis were examined, showing an increase in H+ and Na+ concentrations and a decrease in Mg2+ and Ca2+concentrations. F-, which was not contained in the sample water, was detected after electrolysis accompanying with a reduction of SO42-, Cl- and NO3-. The memory of tritium and ions in the electrolysis cell after electrolysis was possible to be eliminated by washings with de-ionized water. Tritium concentrations of rain at Kumamoto, Japan were determined with a combination of the present electrolytic enrichment system and liquid scintillation counting.