A method of obtaining transuranic elements for nanofuel including: receiving spent nuclear fuel (SNF); separating elements from SNF, including a stream of elements with Z>92, fissile fuel, passive agent, fertile fuel, or fission products; and providing elements. A method of using transuranic elements to create nanofuel, including: receiving, converting, and mixing the transuranic elements with a moderator to obtain nanofuel.

A nanofuel engine including receiving nanofuel (including a molecular mixture, where the molecular mixture includes at least one molecule with dimensions on a nanometer scale) internally in an internal engine that releases nuclear energy, is set forth. A nanofuel chemical composition of fissile fuel, passive agent, and moderator. A method of operating a nanofuel engine loaded with nanofuel in spark or compression ignition mode. A method of cycling a nanofuel engine, including compressing nanofuel; igniting nanofuel; capturing energy released in nanofuel, which is also the working fluid; and using the working fluid to perform mechanical work or generate heat.

A process for recovering uranium from components contaminated with uranium oxide includes providing a cleaning apparatus with a cleaning solution for dissolving the uranium oxide of the components, carrying out a cleaning process by introducing a batch of components into the cleaning apparatus, and carrying out a measurement for determining the uranium content of the components. The cleaning and the measuring are repeated if a limit value for the uranium content is exceeded. The components are discharged from the process if the uranium content falls below a limit value. The cleaning is carried out on a plurality of successive batches of components until a control measurement indicates an unsatisfactory cleaning action of the cleaning solution. The uranium oxide dissolved in the cleaning solution is recovered after indication of the unsatisfactory cleaning action.

According to embodiments, a light water reactor uranium fuel assembly is capable of reducing heating values of both Am-241 and Cm-244, to reduce the amount of generated vitrified waste without using fast reactors. The light water reactor uranium fuel assembly is a light water reactor uranium fuel assembly to be used in a nuclear fuel cycle that extracts. An americium isotope is extracted at the time of reprocessing of spent fuel to be added to a fuel, in which a weight fraction W (unit: wt %) of americium 241 to be added to a fuel heavy metal is in ranges of W<−0.006e.sup.2+0.12e−0.43 (enrichment: 5 wt % or more), W<−0.000356e+0.00357 (enrichment: 4.2 wt % or more and less than 5.0 wt %) with respect to an average enrichment of uranium 235 e (unit: wt %) of the fuel assembly.

The invention provides a system for collecting metal in an electrorefining process, the system having a hollow cathode; and a container defining an upwardly extending surface adapted to be received by the hollow cathode. An embodiment of the invention provides for metal reduction to occur on laterally facing and medially facing surfaces of the cathode such that electrolyte resides between surfaces of the cathode. Also provided is a metal electrorefining process having the steps of subjecting molten salt containing metal moieties to electrolysis wherein reduced metal accumulates in a cathode-cup construct in a first position; raising the construct to a second position above the molten salt while subjecting the construct to heat from the molten salt; withdrawing the cathode from the construct into a vestibule to the electrorefiner to a third position; and removing the cathode and cup from the electrorefiner to a fourth position.

The invention provides a system for collecting metal in an electrorefining process, the system having a hollow cathode; and a container defining an upwardly extending surface adapted to be received by the hollow cathode. An embodiment of the invention provides for metal reduction to occur on laterally facing and medially facing surfaces of the cathode such that electrolyte resides between surfaces of the cathode. Also provided is a metal electrorefining process having the steps of subjecting molten salt containing metal moieties to electrolysis wherein reduced metal accumulates in a cathode-cup construct in a first position; raising the construct to a second position above the molten salt while subjecting the construct to heat from the molten salt; withdrawing the cathode from the construct into a vestibule to the electrorefiner to a third position; and removing the cathode and cup from the electrorefiner to a fourth position.

In a debris trap that may be used in an Emergency Core Cooling System of a nuclear power plant, the filter media is arranged to define both filtration and bypass flowpaths that are in fluid communication with one another. At least initially, each of the filtration and bypass flowpaths are open, and the filtration and bypass flowpaths have relatively low and relatively high head loss, respectively. The debris trap is operative so that flow through the debris trap may passively, and typically gradually, transition from the filtration flowpaths to the bypass flowpath in response to the filter media collecting increasing amounts of debris. More specifically, initially substantially all of the flow may be through the filtration flowpaths, and thereafter the filtration flowpaths may become substantially obstructed so that substantially all of the flow is through the bypass flowpath.

Targetry coupled separation refers to enhancing the production of a predetermined radiation product through the selection of a target (including selection of the target material and the material's physical structure) and separation chemistry in order to optimize the recovery of the predetermined radiation product. This disclosure describes systems and methods for creating (through irradiation) and removing one or more desired radioisotopes from a target and further describes systems and methods that allow the same target to undergo multiple irradiations and separation operations without damage to the target. In contrast with the prior art that requires complete dissolution or destruction of a target before recovery of any irradiation products, the repeated reuse of the same physical target allowed by targetry coupled separation represents a significant increase in efficiency and decrease in cost over the prior art.

Targetry coupled separation refers to enhancing the production of a predetermined radiation product through the selection of a target (including selection of the target material and the material's physical structure) and separation chemistry in order to optimize the recovery of the predetermined radiation product. This disclosure describes systems and methods for creating (through irradiation) and removing one or more desired radioisotopes from a target and further describes systems and methods that allow the same target to undergo multiple irradiations and separation operations without damage to the target. In contrast with the prior art that requires complete dissolution or destruction of a target before recovery of any irradiation products, the repeated reuse of the same physical target allowed by targetry coupled separation represents a significant increase in efficiency and decrease in cost over the prior art.

A material (e.g., an alloy) comprises molybdenum, rhenium, and at least one element selected from the group consisting of tellurium, iodine, selenium, chromium, nickel, copper, titanium, zirconium, tungsten, vanadium, and niobium. Methods of forming the material (e.g., the alloy) comprise mixing molybdenum powder, rhenium powder, and a powder comprising at least one element selected from the group consisting of tellurium, iodine, selenium, chromium, nickel, copper, titanium, zirconium, tungsten, vanadium, and niobium. The mixed powders may be coalesced to form the material (e.g., the alloy).