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DOE on track to deliver high-burnup SNF to Idaho by 2027
The Department of Energy said it anticipated delivering a research cask of high-burnup spent nuclear fuel from Dominion Energy’s North Anna nuclear power plant in Virginia to Idaho National Laboratory by fall 2027. The planned shipment is part of the High Burnup Dry Storage Research Project being conducted by the DOE with the Electric Power Research Institute.
As preparations continue, the DOE said it is working closely with federal agencies as well as tribal and state governments along potential transportation routes to ensure safety, transparency, and readiness every step of the way.
Watch the DOE’s latest video outlining the project here.
Hiroo Numata, Izumi Ohno
Fusion Science and Technology | Volume 38 | Number 2 | September 2000 | Pages 206-223
Technical Paper | doi.org/10.13182/FST00-A143
Articles are hosted by Taylor and Francis Online.
The physicochemical properties of the Pd-H system were studied by in situ potentiometric, resistance, and dilatometric measurements in each of three applied pulse modes, A, B, and C, and repeated H absorption and desorption. Potential, resistance ratio, and an increase in dilation (l/l0) were measured simultaneously after H equilibrium was attained with the Pd electrode. During continuous absorption, structural phase transition ( [right arrow] ) and void formation occurred, and the values of the H/Pd ratio in the limiting phase, in the + phase coexistence, and in the transition and the +voids coexistence regions are consistent with those obtained from the Pd-H isotherm at 40°C. Hydrogen absorption caused the dilation, from whose slope the molar volume was obtained as 0.64 ( phase) and 0.40 ( + phase) cm3/mol. The resistance increased in proportion to the H/Pd ratio and was kept constant at 1.7 to 1.8 over Rtr.For the first absorption through the phase (>min), the electrode potential shifted with an increase in dilation, which suggests nonequilibrium PdH2-x precipitation followed by conversion to the phase and void formation. Although there was a remarkable lack of any dependence on the number of repetitions of the values of the limiting resistance and potential corresponding to the + and + void coexistence, the onset of the phase, min, increased as the number of repetitions increased. The volumetric ratio for an increase in the H/Pd ratio corresponds to the absorption in high-density defect areas surrounding voids. During repeated absorption and desorption in the C applied pulse mode, the apparent molar volumes of the + phase coexistence show that absorption proceeds inhomogenously, in contrast to the first absorption in the A applied pulse mode.