Study of zinc-silver oxide battery system Quarterly report
Silver oxide electrode study and transport parameters of zincate ion through polyethlene separator
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Silver oxide electrode study and transport parameters of zincate ion through polyethlene separator
Electrolyte purity effect on initiation times and growth rate of Zn dendrites in alkaline zincate solution, discussing dendrite initiation retardation
Anisotropic superconducting energy gap of pure Zn from microwave absorption measurements
Anisotropic energy gap model in superconducting Zn to describe microwave absorption measurements
UV irradiation effects on ZnO used as pigment for spacecraft thermal control coatings
Iron cyanide surface additives effect on photodamage to ZnO powder, using ESR method
High impact Ag-Zn cell design for space missions instrument package landing, considering heat sterilization and minimum operational capability
Surface oxide, organic and lead film effects on friction and plastic deformation of Zn single crystal during sliding
Development of battery terminal seal for sealing electrolyte for periods of three to five years is discussed. Operating conditions of battery are defined. Components of electrolyte seal and method of production are reported. Schematic diagrams of device are included.
Unit automatically charges batteries to desired state-of-charge levels, monitors functional battery parameter data both on meters and printer, and automatically activates alarm in event of battery malfunctions. Unit consists of state-of-charge indicator panel, control panel, monitor panel, power panel, charging-current power supply, and load panel.
The effects of a number of cell process and performance variables upon the oxygen evolution rate of silver/silver oxide cathodes are studied to predict and measure the conditions which would result in the production of a minimum of oxygen. The following five tasks comprise the study: the design and fabrication of two pilot test cells to be used for electrode testing; the determination of the sensitivity and accuracy of the test cell; the determination of total volumes and rates of generation by cathodes of standard production procedures; the construction of a sequential test plan; and the construction of a series of positive formation cells in which formation process factors can be controlled.
Theoretical and experimental models for the evaluation of current distribution in flooded, porous electrodes are discussed. An approximation for the local current distribution function was derived for conditions of a linear overpotential, a uniform concentration, and a very conductive matrix. By considering the porous electrode to be an analog of chemical catalyst structures, a dimensionless performance parameter was derived from the approximated current distribution function. In this manner the electrode behavior was characterized in terms of an electrochemical Thiele parameter and an effectiveness factor. It was shown that the electrochemical engineering approach makes possible the organizations of theoretical descriptions and of practical experience in the form of dimensionless parameters, such as the electrochemical Thiele parameters, and hence provides useful information for the design of new electrochemical systems.
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Excitation of the 4d and 5p levels of Zn+ by charge exchange bewteen Ne+ and Zn was investigated. From measured electron temperature and line intensity ratios it was concluded that charge exchange is the dominate mechanism for populating the 4d2D5/2 level of Zn+. Comparison of Zn-Ne and Zn-Ar results imply the same conclusion. No evidence for charge exchange as the dominant pumping mechanism for the 5p2Pl/2, 5p2P3/2, or 4d2D3/2 levels was obtained.
The results of three experimental studies related to the inorganic/organic battery separator operating mechanism are described: saponification of the plasticizer, resistivity of the simulated separators, and zincate diffusion through the separators. The inorganic/organic separator appears to be a particular example of a general class of ionic conducting films composed of inorganic fillers and/or substrates bonded together by an organic polymer containing an incompatible plasticizer that may be leached by the electrolyte. The I/O separator functions as a microporous film of varying tortuosity with essentially no specific chemical inhibition to zincate diffusion.
Over 100 sealed AgO-Zn cells were subjected to prolonged periods of storage over a range of temperatures and storage modes including open circuit, trickle charge, and float charge. Impedances of these cells were monitored throughout, and at the end of the storage period their transient voltage characteristics were observed at the onset of discharge. Results revealed that the impedances of these cells tended to increase with storage time; the magnitude of the impedance rise was dependent primarily on temperature and to a lesser degree on storage mode. Typical values for 50 A-hr cells were usually less than 100 mohm immediately after activation and from 1 to 30 ohm after 6-10 months of storage. Transient voltages of these cells droped sharply during the first msec of discharge and then rose to a stablized value during the following few seconds. The magnitude of the initial drop and the stabilized voltage values were found to be related to impedance but not in a linear manner. The magnitude and duration of the low transient voltages may be unacceptable in some applications of these cells. The impedance variations are attributed to changes occurring at the positive electrode.
Excitation of the 4d and 5p levels of Zn(+) by charge exchange between Ne(+) and Zn was investigated. From measured electron temperature and line intensity ratios it was concluded that charge exchange is the dominant mechanism for populating the 4d 2D5/2 level of Zn(+). Comparison of Zn-Ne and Zn-Ar results imply the same conclusion. No evidence for charge exchange as the dominant pumping mechanism for the 5p 2P1/2, 5p 2P3/2, or 4d 2D3/2 levels was obtained.