Aluminum chlorine battery Final technical report, 27 May 1968 - 26 Mar. 1970

Rechargeable, high energy density battery using molten salt electrolyte and aluminum and chlorine electrode

Aluminum chlorine battery Quarterly report, 27 Apr. - 26 Aug. 1969

Aluminum chlorine batterie

Development of a high capacity toroidal Ni/Cd cell

A nickel cadmium battery design which can offer better thermal management, higher energy density and much lower cost than the state-of-the-art is emphasized. A toroidal Ni/Cd cell concept is described. It was critically reviewed and used to develop two cell designs for practical implementation. One is a double swaged and the other a swaged welded configuration

Aluminum chlorine battery

Rechargeable high energy density battery based on aluminum and chlorine carbon electrodes and molten aluminum chloride-alkali chloride eutectic as electrolyt

Aluminum chlorine battery Quarterly report 27 Aug. - 26 Dec. 1969

Current and electrolyte conductivity measurements of aluminum chlorine batter

Carbon monoxide detector

A sensitive carbon monoxide detector, developed specifically for spacecraft use, is described. An instrument range of 0 to 60 ppm CO in air was devised. The fuel cell type detector is used as a highly sensitive electrolysis cell for electrochemically detecting gases. The concept of an electrochemical CO detector is discussed and the CO oxidation behavior in phosphoric and sulfuric acid electrolytes is reported

Behavior of Metallic Inclusions in Uranium Dioxide

The mobility of micron-size powders of refractory and noble metals in UO{sub 2} was investigated under isothermal and temperature gradient conditions, The metal particles were initially placed between two polished surfaces of UO{sub 2} and any movement which occurred during high temperature annealing was determined microscopically. Tungsten and molybdenum particles 1 to 10 {micro}m in diameter were immobile in UO{sub 2} at 2500°C in a temperature gradient of 1400°C/cm. Ruthenium, however, dissolved into and spread through hypostoichiometric, polycrystalline urania and was found after isothermal annealing as the U-Ru intermetallic compound in the grain boundaries of the oxide. The mechanism does not involve bodily motion of the metal particles. Rather, ruthenium dissolves in the grain bmmdaries of the oxide, migrates as atoms via the same pathway, and reacts while migrating to form URu{sub 3}, This product grows as layers in the grain boundaries. Isothermal ruthenium spreading followed simple diffusion theory, and apparent solubilities and effective diffusivities were obtained from the data for the temperature nmge 2000 to 2300°C. In a temperature gradient, ruthenium moves to the hot zones of UO{sub 2}; the mechanism appears to be the same as found for isothermal spreading, but the extent of movement up the temperature gradient cannot be explained by simple diffusion theory, even with an appreciable Soret effect