This study focuses on techniques that can be used to fuel next generation reactors. The first two studies are new techniques for recycling used nuclear fuel (UNF) and the third is a method of separating uranium (U) from lithium fluoride (LiF) and thorium fluoride (ThF4) salt also known as FLiTh for a thorium (Th) fuel cycle. The first technique proposed for UNF recycling was to use the cladding as an anode to oxidize the zircaloy and dissolve it into a LiF, sodium fluoride (NaF), zirconium fluoride (ZrF4) salt. Zirconium (Zr) was also reduced and deposited on a tungsten (W) cathode at the same time transporting the Zr through the salt. As commercial zircaloy would be contaminated with UNF oxides, and the oxides will not oxidize as part of the electrochemical process, they would be left at the anode as the Zr is dissolved away. This means the deposited Zr, on the cathode, can be disposed of as low-level waste (LLW) or recycled back into the nuclear industry instead of being stored as high-level waste (HLW). The next technique was fluorination of UNF oxides using ZrF4. Using the same LiF-NaF-ZrF4 salt, uranium oxide (UO2), lanthanum oxide (La2O3), and yttrium oxide (Y2O3) were fluorinated into uranium fluoride (UF4), lanthanum fluoride (LaF3), and yttrium fluoride (YF3). By sampling and recording the change in concentration over time, the reaction rate of all three oxides was determined and a temperature dependent reaction rate was reported from 500°C to 650°C. A zirconium oxide (ZrO2) product layer developed on UO2, but it only slowed down the fluorination process but did not stop it. UO2 and Y2O3 fluorinated entirely but La2O3 did not. The solubility limit of LaF3 in the salt was determined to be the reason the reaction did not go to completion. The last technique was the electrochemical separation of U from FLiTh, to simulate irradiated Th that decays to protactinium (Pa). A constant, albeit small current, was used to deposit U on a W electrode without Th depositing with it. A liquid metal bismuth (Bi) electrode was used as well, and a constant current resulted in Th depositing with the U. To get just U to deposit, the current needed to be applied for a time and then no current applied for a time so the system could reach equilibrium. By cycling these two steps it was possible to get U to deposit in Bi without Th. / Doctor of Philosophy / This study focused on techniques useful to the fabrication of next generation reactor fuels. The first focus was on new techniques for recycling used nuclear fuel (UNF). Nuclear waste currently needs to be stored for hundreds of thousands of years to reach background radiotoxicity levels. If plutonium (Pu) is removed from the waste this time is limited to ten thousand years and if the other transuranics (TRU) are removed the waste only needs to be stored for 300 years to reach background radiotoxicity levels. As recycling UNF can make such a drastic difference, developing techniques for this are of utmost importance. The first technique studied was to show that the zirconium (Zr) in zircaloy cladding could be oxidized and transported through salt. This was done by applying a current between a zircaloy anode and tungsten (W) cathode, dissolving the cladding into the salt. The salt used was lithium fluoride (LiF), sodium fluoride (NaF), and zirconium fluoride (ZrF4) salt called FLiNaZr. This transported Zr through the salt and then deposited it on W. If this process was done with zircaloy contaminated with used nuclear fuel (UNF) oxides, the oxides would not dissolve into the salt as part of the process and would be left behind at the anode as Zr is transported through the salt, effectively separating the two. This alone leads to a 25% reduction in the weight of the UNF that needs to be stored. The next technique studied was converting the UNF oxides into fluorides. This was done by having it react with ZrF4 to make zirconium oxide (ZrO2) and UNF fluorides. The oxides studied here were uranium oxide (UO2), yttrium oxide (Y2O3), and lanthanum oxide (La2O3). UO2 and Y2O3 reacted until no material was left but La2O3 did not. This was due to lanthanum fluoride (LaF3) having a solubility limit in the salt that made it impossible for more to be made and stopping the reacting. The reaction rate for each oxide was found and the order of the reaction rates was Y2O3>UO2>La2O3. This process was a success and should be studied more to ensure it will work with all oxides found in UNF. The last technique studied was electrochemically separating uranium (U) from lithium fluoride and thorium fluoride (ThF4) salt. Thorium (Th) is another nuclear material, and while it cannot fission in a reactor it can be turned into an isotope of U, U-233, that can. To do this Th must be irradiated so it turns into protactinium (Pa) which can then be separated from the salt. In this study U was a surrogate for Pa as it is too radioactive to handle in this lab. First, an inert W electrode was used to deposit U metal, and once it was successful a liquid metal bismuth (Bi) electrode was used. A small constant current was able to deposit U on W without co-deposition of Th. For a Bi electrode, an alternating time of applying current and then letting the system rest was needed to deposit U without co-deposition of Th.