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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.
Gregg A. Morgan, Brittany J. Hodge, Anita S. Poore
Fusion Science and Technology | Volume 72 | Number 3 | October 2017 | Pages 426-433
Technical Paper | doi.org/10.1080/15361055.2017.1333858
Articles are hosted by Taylor and Francis Online.
A prototype Pd-Ag diffuser manufactured by Power and Energy was evaluated for performance characterization testing at the Savannah River National Laboratory (SRNL). The prototype Pd-Ag diffuser was characterized to determine the overall performance as a function of the permeation of hydrogen through the membrane. The tests described in this report consider the effects of feed gas compositions, feed flow rates, pump type and internal tube pressure on the permeation of H2 through the Pd-Ag tubes.
For the 96% H2/4% N2 mixtures, nearly all of the H2 permeated through the membrane at flow rates up to 3000 sccm. However, results for the 50% H2/50% N2 composition show that 100% permeation is only achieved up to a flow rate of 1000 sccm. A significant reduction in the hydrogen permeation was observed for the 2% H2/98% N2 composition. This Pd-Ag diffuser design is not suitable for a tritium purification system within the fusion energy fuel cycle. Typical tritium purification systems can be expected to see a range of hydrogen isotope concentrations and this particular prototype diffuser is only suitable for process streams containing high concentrations of hydrogen isotopes.
Significant efforts should be undertaken to identify additional commercial vendors for Pd-Ag diffusers. It is of critical importance to identify, procure, and test different Pd-Ag designs that can perform well over a range of hydrogen isotope concentrations for tritium gas processing applications.