Patent classifications
G21C19/50
ELECTROCHEMICAL CELLS FOR DIRECT OXIDE REDUCTION, AND RELATED METHODS
A method of direct oxide reduction includes forming a molten salt electrolyte in an electrochemical cell, disposing at least one metal oxide in the electrochemical cell, disposing a counter electrode comprising a material selected from the group consisting of osmium, ruthenium, rhodium, iridium, palladium, platinum, silver, gold, lithium iridate, lithium ruthenate, a lithium rhodate, a lithium tin oxygen compound, a lithium manganese compound, strontium ruthenium ternary compounds, calcium iridate, strontium iridate, calcium platinate, strontium platinate, magnesium ruthenate, magnesium iridate, sodium ruthenate, sodium iridate, potassium iridate, and potassium ruthenate in the electrochemical cell, and applying a current between the counter electrode and the at least one metal oxide to reduce the at least one metal oxide. Related methods of direct oxide reduction and related electrochemical cells are also disclosed.
CONTINUOUS REPROCESSING OF SPENT NUCLEAR FUEL
Spent nuclear fuel is added to an electro-reduction cell, wherein the electro-reduction cell includes a halide salt electrolyte, and anode, and a cathode including an alloy of uranium and a first metal forming a low melting point alloy with uranium, the first metal being one or more of: iron; chromium; nickel; manganese; and cobalt. The spent nuclear fuel is electrochemically reduced at a potential sufficient to reduce plutonium and lanthanides in the spent nuclear fuel, to form a molten alloy of the first metal, uranium and higher actinides present in the spent nuclear fuel. The alloy is extracted from the electro-reduction cell while uranium oxide is present in the electro-reduction cell. The spent nuclear fuel includes uranium oxide and at least 1 mol of lanthanides per tonne of uranium in the spent nuclear fuel, and the electro-reduction cell is operated at a temperature above the melting point of the alloy.
CONTINUOUS REPROCESSING OF SPENT NUCLEAR FUEL
Spent nuclear fuel is added to an electro-reduction cell, wherein the electro-reduction cell includes a halide salt electrolyte, and anode, and a cathode including an alloy of uranium and a first metal forming a low melting point alloy with uranium, the first metal being one or more of: iron; chromium; nickel; manganese; and cobalt. The spent nuclear fuel is electrochemically reduced at a potential sufficient to reduce plutonium and lanthanides in the spent nuclear fuel, to form a molten alloy of the first metal, uranium and higher actinides present in the spent nuclear fuel. The alloy is extracted from the electro-reduction cell while uranium oxide is present in the electro-reduction cell. The spent nuclear fuel includes uranium oxide and at least 1 mol of lanthanides per tonne of uranium in the spent nuclear fuel, and the electro-reduction cell is operated at a temperature above the melting point of the alloy.
Electrochemical cells for direct oxide reduction, and related methods
A method of direct oxide reduction includes forming a molten salt electrolyte in an electrochemical cell, disposing at least one metal oxide in the electrochemical cell, disposing a counter electrode comprising a material selected from the group consisting of osmium, ruthenium, rhodium, iridium, palladium, platinum, silver, gold, lithium iridate, lithium ruthenate, a lithium rhodate, a lithium tin oxygen compound, a lithium manganese compound, strontium ruthenium ternary compounds, calcium iridate, strontium iridate, calcium platinate, strontium platinate, magnesium ruthenate, magnesium iridate, sodium ruthenate, sodium iridate, potassium iridate, and potassium ruthenate in the electrochemical cell, and applying a current between the counter electrode and the at least one metal oxide to reduce the at least one metal oxide. Related methods of direct oxide reduction and related electrochemical cells are also disclosed.
Electrochemical cells for direct oxide reduction, and related methods
A method of direct oxide reduction includes forming a molten salt electrolyte in an electrochemical cell, disposing at least one metal oxide in the electrochemical cell, disposing a counter electrode comprising a material selected from the group consisting of osmium, ruthenium, rhodium, iridium, palladium, platinum, silver, gold, lithium iridate, lithium ruthenate, a lithium rhodate, a lithium tin oxygen compound, a lithium manganese compound, strontium ruthenium ternary compounds, calcium iridate, strontium iridate, calcium platinate, strontium platinate, magnesium ruthenate, magnesium iridate, sodium ruthenate, sodium iridate, potassium iridate, and potassium ruthenate in the electrochemical cell, and applying a current between the counter electrode and the at least one metal oxide to reduce the at least one metal oxide. Related methods of direct oxide reduction and related electrochemical cells are also disclosed.
In-vessel rod handling systems
A rod transfer assembly has an outer rotating plug. A pick-up arm assembly extends from the outer rotating plug and includes a pivoting arm. An inner rotating plug is disposed off-center from and within the outer rotating plug and is rotatable independent of a rotation of the outer rotating plug. An access port rotating plug is disposed off-center from and within the inner rotating plug and is rotatable independent of rotation of the outer and inner rotating plugs. A pull arm extends from the access port rotating plug.
In-vessel rod handling systems
A rod transfer assembly has an outer rotating plug. A pick-up arm assembly extends from the outer rotating plug and includes a pivoting arm. An inner rotating plug is disposed off-center from and within the outer rotating plug and is rotatable independent of a rotation of the outer rotating plug. An access port rotating plug is disposed off-center from and within the inner rotating plug and is rotatable independent of rotation of the outer and inner rotating plugs. A pull arm extends from the access port rotating plug.
ANTI-PROLIFERATION SAFEGUARDS FOR NUCLEAR FUEL SALTS
An anti-proliferation technique is disclosed to reduce the likelihood of nuclear proliferation due to the use fissionable fuel salts. The technique includes doping the fuel salt with one or more elements (referred to herein as activation dopants) that, upon exposure to neutrons such as would occur in the fuel salt when a reactor is in operation, undergo a nuclear reaction to, directly or indirectly, form highly active protecting isotopes (of the same element as the activation dopant or a different element). A sufficient mass of activation dopants is used so that the Figure of Merit (FOM) of the fuel salt is decreased to below 1.0 within some target number of days of fission. This allows the FOM of the fuel salt to be controlled so that the fuel becomes too dangerous to handle before to the creation of a significant amount of weaponizable isotopes.
ANTI-PROLIFERATION SAFEGUARDS FOR NUCLEAR FUEL SALTS
An anti-proliferation technique is disclosed to reduce the likelihood of nuclear proliferation due to the use fissionable fuel salts. The technique includes doping the fuel salt with one or more elements (referred to herein as activation dopants) that, upon exposure to neutrons such as would occur in the fuel salt when a reactor is in operation, undergo a nuclear reaction to, directly or indirectly, form highly active protecting isotopes (of the same element as the activation dopant or a different element). A sufficient mass of activation dopants is used so that the Figure of Merit (FOM) of the fuel salt is decreased to below 1.0 within some target number of days of fission. This allows the FOM of the fuel salt to be controlled so that the fuel becomes too dangerous to handle before to the creation of a significant amount of weaponizable isotopes.
ACTINIDE AND RARE EARTH DRAWDOWN SYSTEM FOR MOLTEN SALT RECYCLE
A method for recycling molten salt from electrorefining processes, the method having the steps of collecting actinide metal using a first plurality of cathodes from an electrolyte bath, collecting rare earths metal using a second plurality of cathodes from the electrolyte bath, inserting the collected actinide metal and uranium into the bath, and chlorinating the inserted actinide metal and uranium. Also provided is a system for recycling molten salt, the system having a vessel adapted to receive and heat electrolyte salt, a first plurality of cathodes adapted to be removably inserted into the vessel, a second plurality of cathodes adapted to be removably inserted into the vessel, an anode positioned within the vessel so as to be coaxially aligned with the vessel, and a vehicle for inserting uranium into the salt.