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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.
Alina Niculescu, Gheorghe Bulubașa, George Ana, Ciprian Bucur, Maria Crăciun, Anisia Bornea
Fusion Science and Technology | Volume 80 | Number 3 | May 2024 | Pages 416-421
Research Article | doi.org/10.1080/15361055.2023.2273043
Articles are hosted by Taylor and Francis Online.
A hydrogen generator is used in the combined electrolysis catalytic exchange process (CECE) for low-level tritiated water detritiation as a source of H2 (Q2) for the liquid-phase catalytic exchange column(s) within the process. To produce H2, the H2 generator employs an electrolytic process for H2O splitting into H2 and O2, resulting two streams: a hydrogen stream and an oxygen stream. During the detritiation of water, tritium is accumulated in the H2 generator in the form of tritiated water, and the effluent streams (hydrogen and oxygen) show in time an increased tritium concentration in the form of both tritiated water vapors and gas, which need to be recovered.
The traditional methods for recovery present a risk of explosion due to the high concentration of hydrogen in oxygen (above 3%, while the explosion limit is 1%). In order to minimize this risk, a microchannel reactor with platinated channels has been developed and tested for the oxidation of tritiated hydrogen from the O2 electrolyzer stream in view of its recovery in a scrubber column and returned as tritiated water to the process. The reactor has been coupled to an electrolyzer and tested with regard to the operating temperature. It has been found that it reaches the highest oxidation efficiency of hydrogen when operated at 200°C. The design of the equipment is presented together with the results of the tests done with the equipment integrated in the CECE process.