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  Partner: UNT Libraries Government Documents Department
 Resource Type: Text
 Decade: 1990-1999
ELECTROMOTIVE FORCE, EMF (CELLS)

ELECTROMOTIVE FORCE, EMF (CELLS)

Date: September 16, 1998
Creator: Archer, M. D. & Feldberg, S. W.
Description: The voltage or electric potential difference across the terminals of a cell when no current is drawn from it. The emf of a cell is the sum of the electric potential differences (PDs) produced by a separation of charges (electrons or ions) that can occur at each phase boundary (or interface) in the cell. The magnitude of each PD depends on the chemical nature of the two contacting phases. Thus, at the interface between two different metals, some electrons will have moved from the metal with a higher free energy of electrons to the metal with a lower free energy of electrons. The resultant charge separation will produce a PD (just as charge separation produces a voltage across a capacitor) that, at equilibrium, exactly opposes further electron flow. Similarly, PDs can be produced when electrons partition across a metal/solution interface or metal/solid interface, and when ions partition across a solution/membrane/solution interface.
Contributing Partner: UNT Libraries Government Documents Department
Optical apparatus and method for sensing uranyl

Optical apparatus and method for sensing uranyl

Date: January 1, 1994
Creator: Baylor, L.C. & Buchanan, B.R.
Description: An optical sensing device for uranyl and other substances, a method for making an optical sensing device and a method for chemically binding uranyl and other indicators to glass, quartz, cellulose and similar substrates. The indicator, such as arsenazo III, is immobilized on the substrate using a chemical binding process. The immobilized arsenazo III causes uranyl from a fluid sample to bind irreversibly to the substrate at its active sites, thus causing absorption of a portion of light transmitted through the substrate. Determination of the amount of light absorbed, using conventional means, yields the concentration of uranyl present in the sample fluid. The binding of uranyl on the substrate can be reversed by subsequent exposure of the substrate to a solution of 2,6-pyridinedicarboxylic acid. The chemical binding process is suitable for similarly binding other indicators, such as bromocresol green.
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Composition for detecting uranyl

Composition for detecting uranyl

Date: January 1, 1994
Creator: Baylor, L.C. & Stephens, S.M.
Description: The present invention relates to an indicator composition for use in spectrophotometric detection of a substance in a solution, and a method for making the composition. Useful indicators are sensitive to the particular substance being measured, but are unaffected by the fluid and other chemical species that may be present in the fluid. Optical indicators are used to measure the uranium concentration of process solutions in facilities for extracting uranium from ores, production of nuclear fuels, and reprocessing of irradiated fuels. The composition comprises an organohalide covalently bonded to an indicator for the substance, in such a manner that the product is itself an indicator that provides increased spectral resolution for detecting the substance. The indicator is preferably arsenazo III and the organohalide is preferably cyanuric chloride. These form a composition that is ideally suited for detecting uranyl.
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Method for verification of constituents of a process stream

Method for verification of constituents of a process stream

Date: January 1, 1993
Creator: Baylor, L.C.; Buchanan, B.R. & O`Rourke, P.E.
Description: This invention is comprised of a method for validating a process stream for the presence or absence of a substance of interest such as a chemical warfare agent; that is, for verifying that a chemical warfare agent is present in an input line for feeding the agent into a reaction vessel for destruction, or, in a facility for producing commercial chemical products, that a constituent of the chemical warfare agent has not been substituted for the proper chemical compound. The method includes the steps of transmitting light through a sensor positioned in the feed line just before the chemical constituent in the input line enters the reaction vessel, measuring an optical spectrum of the chemical constituent from the light beam transmitted through it, and comparing the measured spectrum to a reference spectrum of the chemical agent and preferable also reference spectra of surrogates. A signal is given if the chemical agent is not entering a reaction vessel for destruction, or if a constituent of a chemical agent is added to a feed line in substitution of the proper chemical compound.
Contributing Partner: UNT Libraries Government Documents Department
Method for compression of data using single pass LZSS and run-length encoding

Method for compression of data using single pass LZSS and run-length encoding

Date: January 1, 1994
Creator: Berlin, G.J.
Description: A method used preferably with LZSS-based compression methods for compressing a stream of digital data. The method uses a run-length encoding scheme especially suited for data strings of identical data bytes having large run-lengths, such as data representing scanned images. The method reads an input data stream to determine the length of the data strings. Longer data strings are then encoded in one of two ways depending on the length of the string. For data strings having run-lengths less than 18 bytes, a cleared offset and the actual run-length are written to an output buffer and then a run byte is written to the output buffer. For data strings of 18 bytes or longer, a set offset and an encoded run-length are written to the output buffer and then a run byte is written to the output buffer. The encoded run-length is written in two parts obtained by dividing the run length by a factor of 255. The first of two parts of the encoded run-length is the quotient; the second part is the remainder. Data bytes that are not part of data strings of sufficient length are written directly to the output buffer.
Contributing Partner: UNT Libraries Government Documents Department
RPM-SIM (Renewable Energy Power System Modular Simulator) user's guide

RPM-SIM (Renewable Energy Power System Modular Simulator) user's guide

Date: November 15, 1999
Creator: Bialasiewicz, J.T.; Muljadi, E.; Nix, G.R. & Drouilhet, S.
Description: Using the VisSimTM visual environment, researchers developed a modular simulation system to facilitate an application-specific, low-cost study of the system dynamics for wind-diesel hybrid power systems. This manual presents the principal modules of the simulator and, using case studies of a hybrid system, demonstrates some of the benefits that can be gained from understanding the effects of the designer's modifications to these complex dynamic systems.
Contributing Partner: UNT Libraries Government Documents Department
Vitrification of organics-containing wastes

Vitrification of organics-containing wastes

Date: January 1, 1995
Creator: Bickford, D.F.
Description: A process for stabilizing organics-containing waste materials and recovery metals therefrom, and a waste glass product made according to the process are described. Vitrification of wastes such as organic ion exchange resins, electronic components and the like can be accomplished by mixing at least one transition metal oxide with the wastes, and, if needed, glass formers to compensate for a shortage of silicates or other glass formers in the wastes. The transition metal oxide increases the rate of oxidation of organic materials in the wastes to improve the composition of the glass-forming mixture: at low temperatures, the oxide catalyzes oxidation of a portion of the organics in the waste; at higher temperatures, the oxide dissolves and the resulting oxygen ions oxidize more of the organics; and at vitrification temperatures, the metal ions conduct oxygen into the melt to oxidize the remaining organics. In addition, the transition metal oxide buffers the redox potential of the glass melt so that metals such as Au, Pt, Ag, and Cu separate form the melt in the metallic state and can be recovered. After the metals are recovered, the remainder of the melt is allowed to cool and may subsequently be disposed of. The product ...
Contributing Partner: UNT Libraries Government Documents Department
Purge water management system

Purge water management system

Date: January 1995
Creator: Cardoso-Neto, J. E. & Williams, D. W.
Description: A purge water management system is described for effectively eliminating the production of purge water when obtaining a groundwater sample from a monitoring well. In its preferred embodiment, the purge water management system comprises an expandable container, a transportation system, and a return system. The purge water management system is connected to a wellhead sampling configuration, typically permanently installed at the well site. A pump, positioned with the monitoring well, pumps groundwater through the transportation system into the expandable container, which expands in direct proportion with volume of groundwater introduced, usually three or four well volumes, yet prevents the groundwater from coming into contact with the oxygen in the air. After this quantity of groundwater has been removed from the well, a sample is taken from a sampling port, after which the groundwater in the expandable container can be returned to the monitoring well through the return system. The purge water management system prevents the purge water from coming in contact with the outside environment, especially oxygen, which might cause the constituents of the groundwater to oxidize. Therefore, by introducing the purge water back into the monitoring well, the necessity of dealing with the purge water as a hazardous waste ...
Contributing Partner: UNT Libraries Government Documents Department
Method for extracting metals from aqueous waste streams for long term storage

Method for extracting metals from aqueous waste streams for long term storage

Date: January 1, 1993
Creator: Chaiko, D.J.
Description: A liquid-liquid extraction method for removing metals and hydrous metal colloids from waste streams is provided wherein said waste streams are contacted with a solvent system containing a water-in-oil microemulsion wherein the inverted micelles contain the extracted metal. A silicon alkoxide, either alone or in combination with other metal alkoxide compounds is added to the water-in-oil microemulsion, thereby allowing encapsulation of the extracted metal within a silicon oxide network. Lastly, the now-encapsulated metal is precipitated from the water-in-oil microemulsion phase to yield aggregates of metal-silicate particles having average. individual particle sizes of approximately 40 manometers.
Contributing Partner: UNT Libraries Government Documents Department
Starting apparatus for internal combustion engines

Starting apparatus for internal combustion engines

Date: January 1, 1995
Creator: Dyches, G.M. & Dudar, A.M.
Description: This report is a patent description for a system to start an internal combustion engine. Remote starting and starting by hearing impaired persons are addressed. The system monitors the amount of current being drawn by the starter motor to determine when the engine is started. When the engine is started the system automatically deactivates the starter motor. Five figures are included.
Contributing Partner: UNT Libraries Government Documents Department
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