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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.
K. Ichimura, M. Matsuyama, K. Watanabe, T. Takeuchi
Fusion Science and Technology | Volume 8 | Number 2 | September 1985 | Pages 2407-2412
Material Property and Tritium Control | Proceedings of the Second National Topical Meeting on Tritium Technology in Fission, Fusion and Isotopic Applications (Dayton, Ohio, April 30 to May 2, 1985) | doi.org/10.13182/FST85-A24639
Articles are hosted by Taylor and Francis Online.
The rates of ab/desorption of water vapor for Zr-V-Fe getter were investigated by means of mass analyzed thermal desorption spectroscopy. The absorption rate obeyed first order kinetics with respect to the pressure of water vapor. The activation energies for absorption were determined as 1.8 (H2O), 2.7 (D2O), and 3.2 (T2O) kcal/mol. Only hydrogen was desorbed by heating the getter in which water was absorbed. The desorption obeyed second order kinetics with respect to the amount of absorption. The activation energies for desorption were determined as 28.0 (H2O), 28.6 (D2O), and 29.3 (T2O) kcal/mol. It is concluded that the rate determining step for absorption is the dissociation reaction of adsorbed water molecules or hydroxyl groups on the surface. The rate determining step for desorption is the association reaction of hydrogen atoms which diffuse from the bulk to the surface.