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Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
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We encourage you to perform a real-time search of NLEBeta
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1

METHOD OF PREPARING METAL HALIDES  

DOE Patents (OSTI)

The conversion of plutonium halides from plutonium peroxide can be done by washing the peroxide with hydrogen peroxide, drying the peroxide, passing a dry gaseous hydrohalide over the surface of the peroxide at a temperature of about lOO icient laborato C until the reaction rate has stabillzed, and then ralsing the reaction temperature to between 400 and 600 icient laborato C until the conversion to plutonium halide is substantially complete.

Hendrickson, A.V.

1958-11-18T23:59:59.000Z

2

Method for producing hydrocarbon fuels from heavy polynuclear hydrocarbons by use of molten metal halide catalyst  

DOE Patents (OSTI)

In a process for hydrocracking heavy polynuclear carbonaceous feedstocks to produce lighter hydrocarbon fuels by contacting the heavy feedstocks with hydrogen in the presence of a molten metal halide catalyst, thereafter separating at least a substantial portion of the carbonaceous material associated with the reaction mixture from the spent molten metal halide and thereafter regenerating the metal halide catalyst, an improvement comprising contacting the spent molten metal halide catalyst after removal of a major portion of the carbonaceous material therefrom with an additional quantity of hydrogen is disclosed.

Gorin, Everett (San Rafael, CA)

1979-01-01T23:59:59.000Z

3

X-ray Methods in High-Intensity Discharges and Metal-Halide Lamps: X-ray Induced Fluorescence  

SciTech Connect

We describe the use of x-ray induced fluorescence to study metal-halide high-intensity discharge lamps and to measure equilibrium vapor pressures of metal-halide salts. The physical principles of metal-halide lamps, relevant aspects of x-ray-atom interactions, the experimental method using synchrotron radiation, and x-ray induced fluorescence measurements relevant to metal-halide lamps are covered.

Curry, John J.; Lapatovich, Walter P.; Henins, Albert (NIST)

2011-12-09T23:59:59.000Z

4

Method for producing hydrocarbon fuels and fuel gas from heavy polynuclear hydrocarbons by the use of molten metal halide catalysts  

DOE Patents (OSTI)

In a process for hydrocracking heavy polynuclear carbonaceous feedstocks to produce lighter hydrocarbon fuels by contacting the heavy feedstocks with hydrogen in the presence of a molten metal halide catalyst in a hydrocracking zone, thereafter separating at least a major portion of the lighter hydrocarbon fuels from the spent molten metal halide and thereafter regenerating the spent molten metal halide by incinerating the spent molten metal halide by combustion of carbon and sulfur compounds in the spent molten metal halide in an incineration zone, the improvement comprising: (a) contacting the heavy feedstocks and hydrogen in the presence of the molten metal halide in the hydrocracking zone at reaction conditions effective to convert from about 60 to about 90 weight percent of the feedstock to lighter hydrocarbon fuels; (b) separating at least a major portion of the lighter hydrocarbon fuels from the spent molten metal halide; (c) contacting the spent molten metal halide with oxygen in a liquid phase gasification zone at a temperature and pressure sufficient to vaporize from about 25 to about 75 weight percent of the spent metal halide, the oxygen being introduced in an amount sufficient to remove from about 60 to about 90 weight percent of the carbon contained in the spent molten metal halide to produce a fuel gas and regenerated metal halide; and (d) incinerating the spent molten metal halide by combusting carbon and sulfur compounds contained therein.

Gorin, Everett (San Rafael, CA)

1979-01-01T23:59:59.000Z

5

Thermal battery. [solid metal halide electrolytes with enhanced electrical conductance after a phase transition  

DOE Patents (OSTI)

The patent describes an improved thermal battery whose novel design eliminates various disadvantages of previous such devices. Its major features include a halide cathode, a solid metal halide electrolyte which has a substantially greater electrical conductance after a phase transition at some temperature, and a means for heating its electrochemical cells to activation temperature.

Carlsten, R.W.; Nissen, D.A.

1973-03-06T23:59:59.000Z

6

400-Watt Electronic High-Bay Fixture for Metal-Halide High-Intensity Discharge Lighting  

Science Conference Proceedings (OSTI)

The product under assessment is an advanced lighting technology8212a 400-watt, metal-halide, electronic high-intensity discharge (HID) ballast technology designed to be operated as a stand-alone ballast or integrated as a fixture where the ballast becomes part of the fixture mechanical support system.

2008-06-12T23:59:59.000Z

7

Method for hydrocracking a heavy polynuclear hydrocarbonaceous feedstock in the presence of a molten metal halide catalyst  

DOE Patents (OSTI)

A method for hydrocracking a heavy polynuclear hydrocarbonaceous feedstock to produce lighter hydrocarbon fuels by contacting the feedstock with hydrogen in the presence of a molten metal halide catalyst, the method comprising: mixing the feedstock with a heavy naphtha fraction which has an initial boiling point from about 100.degree. to about 160.degree. C. with a boiling point difference between the initial boiling point and the final boiling point of no more than about 50.degree. C. to produce a mixture; thereafter contacting the mixture with partially spent molten metal halide and hydrogen under temperature and pressure conditions so that the temperature is near the critical temperature of the heavy naphtha fraction; separating at least a portion of the heavy naphtha fraction and lighter hydrocarbon fuels from the partially spent molten metal halide, unreacted feedstock and reaction products; thereafter contacting the partially spent molten metal halide, unreacted feedstock and reaction products with hydrogen and fresh molten metal halide in a hydrocracking zone to produce additional lighter hydrocarbon fuels and separating at least a major portion of the lighter hydrocarbon fuels from the spent molten metal halide.

Gorin, Everett (San Rafael, CA)

1981-01-01T23:59:59.000Z

8

Lanthanide-alkali Metal Halide Systems: Characterization and ...  

Science Conference Proceedings (OSTI)

Recovery of Precious Metals from Chloride Media Using Microalgae Waste from Biofuel Extraction Segregation Roasting of a Saprolitic Laterite Ore: An...

9

LaNi{sub 5}-based metal hydride electrode in Ni-MH rechargeable cells  

DOE Patents (OSTI)

An at least ternary metal alloy of the formula AB{sub (Z-Y)}X{sub (Y)} is disclosed. In this formula, A is selected from the rare earth elements, B is selected from the elements of Groups 8, 9, and 10 of the Periodic Table of the Elements, and X includes at least one of the following: antimony, arsenic, germanium, tin or bismuth. Z is greater than or equal to 4.8 and less than or equal to 6.0. Y is greater than 0 and less than 1. Ternary or higher-order substitutions to the base AB{sub 5} alloys that form strong kinetic interactions with the predominant metals in the base metal hydride are used to form metal alloys with high structural integrity after multiple cycles of hydrogen sorption. 16 figs.

Bugga, R.V.; Fultz, B.; Bowman, R.; Surampudi, S.R.; Witham, C.K.; Hightower, A.

1999-03-30T23:59:59.000Z

10

Alkaline and alkaline earth metal phosphate halides and phosphors  

SciTech Connect

Compounds, phosphor materials and apparatus related to nacaphite family of materials are presented. Potassium and rubidium based nacaphite family compounds and phosphors designed by doping divalent rare earth elements in the sites of alkaline earth metals in the nacaphite material families are descried. An apparatus comprising the phosphors based on the nacaphite family materials are presented herein. The compounds presented is of formula A.sub.2B.sub.1-yR.sub.yPO.sub.4X where the elements A, B, R, X and suffix y are defined such that A is potassium, rubidium, or a combination of potassium and rubidium and B is calcium, strontium, barium, or a combination of any of calcium, strontium and barium. X is fluorine, chlorine, or a combination of fluorine and chlorine, R is europium, samarium, ytterbium, or a combination of any of europium, samarium, and ytterbium, and y ranges from 0 to about 0.1.

Lyons, Robert Joseph; Setlur, Anant Achyut; Cleaver, Robert John

2012-11-13T23:59:59.000Z

11

Transition metal ion-assisted photochemical generation of alkyl halides and hydrocarbons from carboxylic acids  

Science Conference Proceedings (OSTI)

Near-UV photolysis of aqueous solutions of propionic acid and aqueous Fe3+ in the absence of oxygen generates a mixture of hydrocarbons (ethane, ethylene and butane), carbon dioxide, and Fe2+. The reaction becomes mildly catalytic (about five turnovers) in the presence of oxygen which converts a portion of alkyl radicals to oxidizing intermediates that reoxidize Fe2+. The photochemistry in the presence of halide ions (X? = Cl?, Br?) generates ethyl halides via halogen atom abstraction from FeXn3?n by ethyl radicals. Near-quantitative yields of C2H5X are obtained at ?0.05 M X?. Competition experiments with Co(NH3)5Br2+ provided kinetic data for the reaction of ethyl radicals with FeCl2+ (k = (4.0 0.5) 106 M?1 s?1) and with FeBr2+ (k = (3.0 0.5) 107 M?1 s?1). Photochemical decarboxylation of propionic acid in the presence of Cu2+ generates ethylene and Cu+. Longer-chain acids also yield alpha olefins as exclusive products. These reactions become catalytic under constant purge with oxygen which plays a dual role. It reoxidizes Cu+ to Cu2+, and removes gaseous olefins to prevent accumulation of Cu+(olefin) complexes and depletion of Cu2+. The results underscore the profound effect that the choice of metal ions, the medium, and reaction conditions exert on the photochemistry of carboxylic acids.

Carraher, Jack; Pestovsky, Oleg; Bakac, Andreja

2012-03-14T23:59:59.000Z

12

Silicon halide-alkali metal flames as a source of solar grade silicon. Final report  

DOE Green Energy (OSTI)

The object of this program was to determine the feasibility of using continuous high-temperature reactions of alkali metals and silicon halides to produce silicon in large quantities and of suitable purity for use in the production of photovoltaic solar cells. Equilibrium calculations showed that a range of conditions were available where silicon was produced as a condensed phase but the byproduct alkali metal salt was a vapor. A process was proposed using the vapor phase reaction of Na with SiCl/sub 4/. Low pressure experiments were performed demonstrating that free silicon was produced and providing experience with the construction of reactant vapor generators. Further experiments at higher reagent flow rates were performed in a low temperature flow tube configuration with co-axial injection of reagents. Relatively pure silicon was produced in these experiments. A high temperature graphite flow tube was built and continuous separation of Si from NaCl was demonstrated. A larger-scaled well-stirred reactor was built. Experiments were performed to investigate the compatibility of graphite-based reactor materials of construction with sodium. At 1100 to 1200 K none of these materials were found to be suitable. At 1700 K the graphites performed well with little damage except to coatings of pyrolytic graphite and silicon carbide which were damaged.

Olson, D.B.; Miller, W.J.; Gould, R.K.

1980-01-01T23:59:59.000Z

13

Technetium Dichloride: A New Binary Halide Containing Metal-Metal Multiple Bonds  

Science Conference Proceedings (OSTI)

Technetium dichloride has been discovered. It was synthesized from the elements and characterized by several physical techniques, including single crystal X-ray diffraction. In the solid state, technetium dichloride exhibits a new structure type consisting of infinite chains of face sharing [Tc{sub 2}Cl{sub 8}] rectangular prisms that are packed in a commensurate supercell. The metal-metal separation in the prisms is 2.127(2) {angstrom}, a distance consistent with the presence of a Tc {triple_bond} Tc triple bond that is also supported by electronic structure calculations.

Poineau, Frederic; Malliakas, Christos D.; Weck, Philippe F.; Scott, Brian L.; Johnstone, Erik V.; Forster, Paul M.; Kim, Eunja; Kanatzidis, Mercouri G.; Czerwinski, Kenneth R.; Sattelberge, Alfred P. (UNLV); (NWU); (LANL)

2011-10-19T23:59:59.000Z

14

Technetium dichloride : a new binary halide containing metal-metal multiple bonds.  

Science Conference Proceedings (OSTI)

Technetium dichloride has been discovered. It was synthesized from the elements and characterized by several physical techniques, including single crystal X-ray diffraction. In the solid state, technetium dichloride exhibits a new structure type consisting of infinite chains of face sharing [Tc{sub 2}Cl{sub 8}] rectangular prisms that are packed in a commensurate supercell. The metal-metal separation in the prisms is 2.127(2) {angstrom}, a distance consistent with the presence of a Tc {triple_bond} Tc triple bond that is also supported by electronic structure calculations.

Poineau, F.; Malliakas, C. D.; Weck, P. F.; Scott, B. L.; Johnstone, E. V.; Forster, P. M.; Kim, E.; Kanatzidis, M. G.; Czerwinski, K. R.; Sattelberger, A. P. (Materials Science Division); ( OTD-EESA); (Univ. of Nevada at Las Vegas); (LANL); (Northwestern Univ.)

2011-06-15T23:59:59.000Z

15

MH  

NLE Websites -- All DOE Office Websites (Extended Search)

Martin B. Hecht phone: 630252-8264 fax: 630252-3903 e-mail: hecht@theory.phy.anl.gov Biographical sketch 1993 Bachelor of Science, University of Adelaide, Australia 1994 Bachelor...

16

Actinide halide complexes  

DOE Patents (OSTI)

A compound of the formula MX{sub n}L{sub m} wherein M = Th, Pu, Np,or Am thorium, X = a halide atom, n = 3 or 4, L is a coordinating ligand selected from the group consisting of aprotic Lewis bases having an oxygen-, nitrogen-, sulfur-, or phosphorus-donor, and m is 3 or 4 for monodentate ligands or is 2 for bidentate ligands, where n + m = 7 or 8 for monodentate ligands or 5 or 6 for bidentate ligands, a compound of the formula MX{sub n} wherein M, X, and n are as previously defined, and a process of preparing such actinide metal compounds including admixing the actinide metal in an aprotic Lewis base as a coordinating solvent in the presence of a halogen-containing oxidant, are provided.

Avens, L.R.; Zwick, B.D.; Sattelberger, A.P.; Clark, D.L.; Watkin, J.G.

1991-02-07T23:59:59.000Z

17

Oxidation of hydrogen halides to elemental halogens  

DOE Patents (OSTI)

A process for oxidizing hydrogen halides having substantially no sulfur impurities by means of a catalytically active molten salt is disclosed. A mixture of the subject hydrogen halide and an oxygen bearing gas is contacted with a molten salt containing an oxidizing catalyst and alkali metal normal sulfates and pyrosulfates to produce an effluent gas stream rich in the elemental halogen and substantially free of sulfur oxide gases.

Rohrmann, Charles A. (Kennewick, WA); Fullam, Harold T. (Richland, WA)

1985-01-01T23:59:59.000Z

18

Actinide halide complexes  

DOE Patents (OSTI)

A compound is described of the formula MX[sub n]L[sub m] wherein M is a metal atom selected from the group consisting of thorium, plutonium, neptunium or americium, X is a halide atom, n is an integer selected from the group of three or four, L is a coordinating ligand selected from the group consisting of aprotic Lewis bases having an oxygen-, nitrogen-, sulfur-, or phosphorus-donor, and m is an integer selected from the group of three or four for monodentate ligands or is the integer two for bidentate ligands, where the sum of n+m equals seven or eight for monodentate ligands or five or six for bidentate ligands. A compound of the formula MX[sub n] wherein M, X, and n are as previously defined, and a process of preparing such actinide metal compounds are described including admixing the actinide metal in an aprotic Lewis base as a coordinating solvent in the presence of a halogen-containing oxidant.

Avens, L.R.; Zwick, B.D.; Sattelberger, A.P.; Clark, D.L.; Watkin, J.G.

1992-11-24T23:59:59.000Z

19

Actinide halide complexes  

DOE Patents (OSTI)

A compound of the formula MX.sub.n L.sub.m wherein M is a metal atom selected from the group consisting of thorium, plutonium, neptunium or americium, X is a halide atom, n is an integer selected from the group of three or four, L is a coordinating ligand selected from the group consisting of aprotic Lewis bases having an oxygen-, nitrogen-, sulfur-, or phosphorus-donor, and m is an integer selected from the group of three or four for monodentate ligands or is the integer two for bidentate ligands, where the sum of n+m equals seven or eight for monodentate ligands or five or six for bidentate ligands, a compound of the formula MX.sub.n wherein M, X, and n are as previously defined, and a process of preparing such actinide metal compounds including admixing the actinide metal in an aprotic Lewis base as a coordinating solvent in the presence of a halogen-containing oxidant, are provided.

Avens, Larry R. (Los Alamos, NM); Zwick, Bill D. (Santa Fe, NM); Sattelberger, Alfred P. (Los Alamos, NM); Clark, David L. (Los Alamos, NM); Watkin, John G. (Los Alamos, NM)

1992-01-01T23:59:59.000Z

20

Development of processes for the production of solar grade silicon from halides and alkali metals. First quarterly report, October 3-December 31, 1979  

DOE Green Energy (OSTI)

This program is directed toward the development of processes involving high temperature reactions of silicon halides with alkali metals for the production of solar grade silicon in volume at low cost. Experiments are being performed to evaluate product separation and collection processes, measure heat release parameters for scaling purposes, determine the effects of reactants and/or products on materials of reactor construction, and make preliminary engineering and economic analyses of a scaled-up process. Samples of the silicon product will be delivered to JPL for evaluation of solar cell performance. During this reporting period the silicon reactor test apparatus reached operational capabilities after a shutdown for two months. Several design improvements were made while returning it to an operational stage. During the initial series of experiments complete product separation of the silicon from the salt was achieved and small samples (approx. = 3 to 40 g) of fused silicon were collected. The test apparatus is now being operated on a routine basis for periods of about twenty minutes. Finally, the initial work began on the engineering and economic analysis for scale-up of the silicon production process.

Dickson, C.R.; Gould, R.K.

1980-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Implications of NiMH Hysteresis on HEV Battery Testing and Performance  

SciTech Connect

Nickel Metal-Hydride (NiMH) is an advanced high-power battery technology that is presently employed in Hybrid Electric Vehicles (HEVs) and is one of several technologies undergoing continuing research and development by FreedomCAR. Unlike some other HEV battery technologies, NiMH exhibits a strong hysteresis effect upon charge and discharge. This hysteresis has a profound impact on the ability to monitor state-of-charge and battery performance. Researchers at the Idaho National Engineering and Environmental Laboratory (INEEL) have been investigating the implications of NiMH hysteresis on HEV battery testing and performance. Experimental results, insights, and recommendations are presented.

Motloch, Chester George; Belt, Jeffrey R; Hunt, Gary Lynn; Ashton, Clair Kirkendall; Murphy, Timothy Collins; Miller, Ted J.; Coates, Calvin; Tataria, H. S.; Lucas, Glenn E.; Duong, T.Q.; Barnes, J.A.; Sutula, Raymond

2002-08-01T23:59:59.000Z

22

APPARATUS FOR THE PRODUCTION OF LITHIUM METAL  

DOE Patents (OSTI)

Methods and apparatus for the production of high-purity lithium from lithium halides are described. The apparatus is provided for continuously contacting a molten lithium halide with molten barium, thereby forming lithium metal and a barium halide, establishing separate layers of these reaction products and unreacted barium and lithium halide, and continuously withdrawing lithium and barium halide from the reaction zone. (AEC)

Baker, P.S.; Duncan, F.R.; Greene, H.B.

1961-08-22T23:59:59.000Z

23

Photochemical studies of alkali halide vapors  

SciTech Connect

Thesis. An apparatus has been constructed for studying the photodissociation of alkali halides to produce excited alkali metal atoms. The key component is a low pressure H/sub 2/ arc continuum uv source. Radiation from this source, modulated by a chopping wheel and analyzed by a monochromator, enters a cell containing the alkali halide vapor. In the appropriate wavelength range, photodissociation occurs to produce the alkali atom in an excited /sup 2/p state, the flourescence from which is detected by a photomultiplier-lock-in amplifier combination. (auth)

Earl, B.L.

1973-08-01T23:59:59.000Z

24

1999 Toyota RAV 4 EV Performance Characterization: Panasonic NiMH Battery -- Conductive Charging  

Science Conference Proceedings (OSTI)

This report characterizes the performance of the 1998 and 1999 Toyota RAV 4 conductively-charged electric vehicle models equipped with Panasonic Nickel Metal Hydride (NiMH) batteries. The tests performed were: weight certification, range, state of charge meter evaluation, sound level, acceleration, maximum speed, braking, power quality evaluation, and charger performance.

1999-12-16T23:59:59.000Z

25

1999 Toyota RAV 4 EV Performance Characterization: Panasonic NiMH Battery -- Inductive Charging  

Science Conference Proceedings (OSTI)

This report characterizes the performance of a 1999 Toyota RAV 4 inductively-charged electric vehicle equipped with Panasonic Nickel Metal Hydride (NiMH) batteries. The tests performed were weight certification, range, vehicle performance, sound level tests, power quality evaluation, state of charge meter evaluation, and charger performance.

1999-12-15T23:59:59.000Z

26

PREPARATION OF HALIDES OF PLUTONIUM  

DOE Patents (OSTI)

A dry chemical method is described for preparing plutonium halides, which consists in contacting plutonyl nitrate with dry gaseous HCl or HF at an elevated temperature. The addition to the reaction gas of a small quantity of an oxidizing gas or a reducing gas will cause formation of the tetra- or tri-halide of plutonium as desired.

Garner, C.S.; Johns, I.B.

1958-09-01T23:59:59.000Z

27

Process for oxidation of hydrogen halides to elemental halogens  

DOE Patents (OSTI)

An improved process for generating an elemental halogen selected from chlorine, bromine or iodine, from a corresponding hydrogen halide by absorbing a molten salt mixture, which includes sulfur, alkali metals and oxygen with a sulfur to metal molar ratio between 0.9 and 1.1 and includes a dissolved oxygen compound capable of reacting with hydrogen halide to produce elemental halogen, into a porous, relatively inert substrate to produce a substrate-supported salt mixture. Thereafter, the substrate-supported salt mixture is contacted (stage 1) with a hydrogen halide while maintaining the substrate-supported salt mixture during the contacting at an elevated temperature sufficient to sustain a reaction between the oxygen compound and the hydrogen halide to produce a gaseous elemental halogen product. This is followed by purging the substrate-supported salt mixture with steam (stage 2) thereby recovering any unreacted hydrogen halide and additional elemental halogen for recycle to stage 1. The dissolved oxygen compound is regenerated in a high temperature (stage 3) and an optical intermediate temperature stage (stage 4) by contacting the substrate-supported salt mixture with a gas containing oxygen whereby the dissolved oxygen compound in the substrate-supported salt mixture is regenerated by being oxidized to a higher valence state.

Lyke, Stephen E. (Middleton, WI)

1992-01-01T23:59:59.000Z

28

ELECTROLYTIC PROCESS FOR PRODUCING METALS  

DOE Patents (OSTI)

A method is described for reducing beryllium halides to beryllium. The beryllfum halide fs placed in an eutectic mixture of alkali halides and alkaline earth halides. The constituents of this eutectic bath are so chosen that it has a melting point less than the boiling point of mercury, which acts as a cathode for the system. The beryllium metal is then deposited in the mercury upon electrolysis.

Kopelman, B.; Holden, R.B.

1961-06-01T23:59:59.000Z

29

Oxidation of hydrogen halides to elemental halogens with catalytic molten salt mixtures  

DOE Patents (OSTI)

A process for oxidizing hydrogen halides by means of a catalytically active molten salt is disclosed. The subject hydrogen halide is contacted with a molten salt containing an oxygen compound of vanadium and alkali metal sulfates and pyrosulfates to produce an effluent gas stream rich in the elemental halogen. The reduced vanadium which remains after this contacting is regenerated to the active higher valence state by contacting the spent molten salt with a stream of oxygen-bearing gas.

Rohrmann, Charles A. (Kennewick, WA)

1978-01-01T23:59:59.000Z

30

RARE-EARTH METAL FISSION PRODUCTS FROM LIQUID U-Bi  

DOE Patents (OSTI)

Fission product metals can be removed from solution in liquid bismuth without removal of an appreciable quantity of uranium by contacting the liquid metal solution with fused halides, as for example, the halides of sodium, potassium, and lithium and by adding to the contacted phases a quantity of a halide which is unstable relative to the halides of the fission products, a specific unstable halide being MgCl/sub 3/.

Wiswall, R.H.

1960-05-10T23:59:59.000Z

31

Lanthanide doped strontium barium mixed halide scintillators  

DOE Patents (OSTI)

The present invention provides for a composition comprising an inorganic scintillator comprising a lanthanide-doped strontium barium mixed halide useful for detecting nuclear material.

Gundiah, Gautam; Bizarri, Gregory; Hanrahan, Stephen M; Bourret-Courchesne, Edith; Derenzo, Stephen E

2013-07-16T23:59:59.000Z

32

PROCESSING OF URANIUM-METAL-CONTAINING FUEL ELEMENTS  

DOE Patents (OSTI)

A process is given for recovering uranium from neutronbombarded uranium- aluminum alloys. The alloy is dissolved in an aluminum halide--alkali metal halide mixture in which the halide is a mixture of chloride and bromide, the aluminum halide is present in about stoichiometric quantity as to uranium and fission products and the alkali metal halide in a predominant quantity; the uranium- and electropositive fission-products-containing salt phase is separated from the electronegative-containing metal phase; more aluminum halide is added to the salt phase to obtain equimolarity as to the alkali metal halide; adding an excess of aluminum metal whereby uranium metal is formed and alloyed with the excess aluminum; and separating the uranium-aluminum alloy from the fission- productscontaining salt phase. (AEC)

Moore, R.H.

1962-10-01T23:59:59.000Z

33

APPARATUS FOR HIGH PURITY METAL RECOVERY  

DOE Patents (OSTI)

An apparatus is described for preparing high purity metal such as uranium, plutonium and the like from an impure mass of the same metal. The apparatus is arranged so that the impure metal is heated and swept by a stream of hydrogen gas bearing a halogen such as iodine. The volatiie metal halide formed is carried on to a hot filament where the metal halide is decomposed and the molten high purity metal is collected in a rceeiver below

Magel, T.T.

1959-02-10T23:59:59.000Z

34

Browse wiki | Open Energy Information  

Open Energy Info (EERE)

OpenEIUtilityRateBasicInformationComments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH),...

35

Rare Earth Metal research, at DOE  

Office of Scientific and Technical Information (OSTI)

Energy Citations Database - Intermultiplet transitions in rare-earth metals DOE Green Energy - LaNi.sub.5 is-based metal hydride electrode in Ni-MH rechargeable cells...

36

Faster Dissociation: Aryl Halide Radical Anions  

NLE Websites -- All DOE Office Websites (Extended Search)

Faster Dissociation: Measured Rates and Computed Effects on Barriers in Faster Dissociation: Measured Rates and Computed Effects on Barriers in Aryl Halide Radical Anions Norihiko Takeda, Pavel V. Poliakov, Andrew R. Cook, and John R. Miller J. Am. Chem. Soc. 126, 4301-4309 (2004). [Find paper at ACS Publications] Abstract: Carbon-halogen bond dissociation rates for a series of aryl halide radical anions (ArX-·: X = Cl, Br) in NMP were measured at room temperature by pulse radiolysis with 10-11 s time resolution. To obtain accurate dissociation rates, care was taken to measure and correct for competing decay channels. The observed rates correlated well with activation energies computed in the gas phase by density functional (DFT) calculations. The rates did not correlate well with electron affinities or dissociation energies obtained by the same computational methods, although such

37

Lanthanide-halide based humidity indicators  

SciTech Connect

The present invention discloses a lanthanide-halide based humidity indicator and method of producing such indicator. The color of the present invention indicates the humidity of an atmosphere to which it is exposed. For example, impregnating an adsorbent support such as silica gel with an aqueous solution of the europium-containing reagent solution described herein, and dehydrating the support to dryness forms a substance with a yellow color. When this substance is exposed to a humid atmosphere the water vapor from the air is adsorbed into the coating on the pore surface of the silica gel. As the water content of the coating increases, the visual color of the coated silica gel changes from yellow to white. The color change is due to the water combining with the lanthanide-halide complex on the pores of the gel.

Beitz, James V. (Hinsdale, IL); Williams, Clayton W. (Chicago, IL)

2008-01-01T23:59:59.000Z

38

HIGGS BOSON SEARCH AT PHOTON COLLIDER FOR MH = 140 ? 190 GEV.  

E-Print Network (OSTI)

A Higgs boson within the mass range MH = 140 ? 190 GeV can be discovered at a photon collider in the reaction ?? ? WW (with real or virtual W). Quite moderate resolution in the effective mass of the WW system is required. Preliminary remarks. A discovery of the Higgs boson is one of the main goals for the next generation of colliders. If the Higgs boson mass MH is larger than 2MZ, Higgs boson can be discovered at LHC, photon colliders [1] or e + e ? linear colliders [2] via the sizable decay mode H ? ZZ. For all types of collisions a background to this decay mode is rather small. If MH Higgs boson can be discovered at photon colliders or e + e ? linear colliders via the dominant decay mode H ? b b and at LHC via the decay mode H ? ??. The mass range MH = 140 ? 190 GeV is the most difficult one for the Higgs boson discovery. In this mass range the decay mode H ? W + W ? with real or virtual Ws (W ? ? qq, e?,...) is dominant, branching ratios of other decay modes decrease rapidly and their using for the Higgs boson discovery is very difficult. The use of the H ? W + W ? decay at e + e ?

unknown authors

1997-01-01T23:59:59.000Z

39

HIGGS BOSON SEARCH AT PHOTON COLLIDER FOR MH = 140 ? 190 GEV.  

E-Print Network (OSTI)

A Higgs boson within the mass range MH = 140 ? 190 GeV can be discovered at a photon collider in the reaction ?? ? WW (with real or virtual W) with the luminosity integral about 1 fb ?1. The reasonable resolution in the effective mass of the WW system is required. Preliminary remarks. A discovery of the Higgs boson is one of the main goals for the next generation of colliders. If the Higgs boson mass MH is larger than 2MZ, it can be discovered at LHC, photon colliders [1] or e + e ? linear colliders [2] via the sizable decay mode H ? ZZ. For all types of collisions a background to this decay mode is rather small. If MH Higgs boson can be discovered at e + e ? linear colliders or photon colliders via the dominant decay mode H ? b b and at LHC via the decay mode H ? ??. The mass range MH = 140 ? 190 GeV is the most difficult one for the Higgs boson discovery. In this mass range the decay mode H ? W + W ? with real or virtual Ws

unknown authors

1997-01-01T23:59:59.000Z

40

METHOD FOR THE PREPARATION OF PLUTONIUM HALIDES AND OXYHALIDES  

DOE Patents (OSTI)

Plutonium trihalide or plutonium(III) oxyhalide is prepared by reacting plutonium dioxide with hydrogen halide at 300 to 1000 deg C in the presence of hydrogen, ammonium iodide, or ammonium bromide.

Davidson, N.R.; Katz, J.J.

1960-02-23T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Planar Sodium Metal Halide Battery for Renewable Integration and ...  

Science Conference Proceedings (OSTI)

In this work we will present a sodium ߔ-alumina cell designed for widespread renewable energy integration and electrical grid applications. The new generation...

42

Spectroscopy on Metal-Halide Lamps under Varying Gravity Conditions  

E-Print Network (OSTI)

orange street lighting), which has a slightly lower discharge conversion efficiency, but the 589 nm line. They are mainly used for applications where a high light output is desired; examples are shop lighting, street. Haverlag Copromotor: dr.ir. W.W. Stoffels Copyright c 2008 by A.J. Flikweert This research was financially

Eindhoven, Technische Universiteit

43

Characteristics of the high-rate discharge capability of a nickel/metal hydride battery electrode  

Science Conference Proceedings (OSTI)

The high rate discharge capability of the negative electrode in a Ni/MH battery is mainly determined by the charge transfer process at the interface between the metal hydride (MH) alloy powder and the electrolyte, and the mass transfer process in the bulk MH alloy powder. In this study, the anodic polarization curves of a MH electrode were measured and analyzed. An alloy of nominal composition Mm{sub 0.95}Ti{sub 0.05}Ni{sub 3.85}Co{sub 0.45}Mn{sub 0.35}Al{sub 0.35} was used as the negative electrode material. With increasing number of charge/discharge cycles, the MH alloy powders microcrack into particles several micrometers in diameter. The decrease in the MH alloy particle size results in an increase in both the activation surface area and the exchange current density of the MH alloy electrode. The electrode overpotentials of the MH electrode decreases with increasing number of cycles at a large value of anodic polarization current. The decrease in electrode overpotential leads to an increase in the high rate discharge capability of the MH electrode. By using the limiting current, the hydrogen diffusion coefficient in the MH alloy was estimated to be 1.2 x 10{sup {minus}11}cm{sup 2}s{sup {minus}1} assuming an average particle radius of 5 {micro}m.

Geng, M.; Han, J.; Feng, F.; Northwood, D.O.

1999-10-01T23:59:59.000Z

44

A Solid-State 199Hg NMR Study of Mercury Halides  

E-Print Network (OSTI)

red polymorph) suggest that the mercury is in sites of cubicTable III. NMR Properties of Mercury Halide Nuclei a IsotopeState 199 Hg NMR Study of Mercury Halides R. E. Taylor 1 *,

Taylor, Robert E; Bai, Shi; Dybowski, Cecil

2011-01-01T23:59:59.000Z

45

Regeneration of zinc halide catalyst used in the hydrocracking of polynuclear hydrocarbons  

DOE Patents (OSTI)

Improved recovery of spent molten zinc halide hydro-cracking catalyst is achieved in the oxidative vapor phase regeneration thereof by selective treatment of the zinc oxide carried over by the effluent vapors from the regeneration zone with hydrogen halide gas under conditions favoring the reaction of the zinc oxide with the hydrogen halide, whereby regenerated zinc halide is recovered in a solids-free state with little loss of zinc values.

Gorin, Everett (San Rafael, CA)

1978-01-01T23:59:59.000Z

46

Method for calcining nuclear waste solutions containing zirconium and halides  

DOE Patents (OSTI)

A reduction in the quantity of gelatinous solids which are formed in aqueous zirconium-fluoride nuclear reprocessing waste solutions by calcium nitrate added to suppress halide volatility during calcination of the solution while further suppressing chloride volatility is achieved by increasing the aluminum to fluoride mole ratio in the waste solution prior to adding the calcium nitrate.

Newby, Billie J. (Idaho Falls, ID)

1979-01-01T23:59:59.000Z

47

Max Tech and Beyond: High-Intensity Discharge Lamps  

E-Print Network (OSTI)

the reason industry started by developing ceramic MH lampsceramic metal halide lamps, which are the focus of industryindustry had invested in the development of very low wattage ceramic

Scholand, Michael

2012-01-01T23:59:59.000Z

48

Beyond child's play : wealth, status, and the death of children in the MH-LH I periods of the Argolid, Greece.  

E-Print Network (OSTI)

??This study explores the mortuary remains of children from the MH-LH I periods of the Argolid, Greece. This examination concentrates on how the child in (more)

Schleifer, Katherine

2010-01-01T23:59:59.000Z

49

SEPARATION OF METAL SALTS BY ADSORPTION  

DOE Patents (OSTI)

It has been found that certain metal salts, particularly the halides of iron, cobalt, nickel, and the actinide metals, arc readily absorbed on aluminum oxide, while certain other salts, particularly rare earth metal halides, are not so absorbed. Use is made of this discovery to separate uranium from the rare earths. The metal salts are first dissolved in a molten mixture of alkali metal nitrates, e.g., the eutectic mixture of lithium nitrate and potassium nitrate, and then the molten salt solution is contacted with alumina, either by slurrying or by passing the salt solution through an absorption tower. The process is particularly valuable for the separation of actinides from lanthanum-group rare earths.

Gruen, D.M.

1959-01-20T23:59:59.000Z

50

Ultrasonic Relaxation in Ethanol?Ethyl Halide Mixtures  

Science Conference Proceedings (OSTI)

Ultrasonic studies in mixtures of ethanol and various ethyl halides show that maxima exist in the plots of the absorption coefficient versus concentration. These maxima are located at relatively small ethanol concentrations. The measurements made include a detailed investigation of the temperature and frequency dependence of the absorption in the ethanol?ethyl chloride system and somewhat less complete studies of the ethanol?ethyl bromide and ethanol?ethyl iodide systems. In each of the systems the measurements were made as a function of concentration. The results in the ethanol?ethyl chloride mixtures indicate the presence of a single relaxation process occurring in the range of measurement (15?165 MHz). The mechanism for this relaxation process is considered both in terms of a quasichemical association theory and in terms of a fluctuating concentration theory. The suggestion is made that the relaxational behavior may be connected with the existence azeotropic concentrations in these mixtures.

V. A. Solovyev; C. J. Montrose; M. H. Watkins; T. A. Litovitz

1968-01-01T23:59:59.000Z

51

THE STABILITY AND REVERSIBILITY OF METALLIC BOROHYDRIDES  

DOE Green Energy (OSTI)

In effort to develop reversible metallic borohydrides with high hydrogen storage capacity and low dehydriding temperature, several new materials have been synthesized by modifying LiBH{sub 4} with various metal halides and hydrides. The investigation shows that the halide modification effectively reduced the dehydriding temperature through ion exchange interaction. The effective halides are TiCl{sub 3}, TiF{sub 3}, ZnF{sub 2} and AlF{sub 3}. The material LiBH{sub 4}+0.1TiF{sub 3} desorbs 3.5wt% and 8.5wt% hydrogen at 150 C and 450 C respectively. It re-absorbed 6wt% hydrogen at 500 C and 70 bar after dehydrogenation. The XRD of the rehydrided samples confirmed the formation of LiBH{sub 4}. It indicates that the materials are reversible at the conditions given. However, a number of other halides: MgF{sub 2}, MgCl{sub 2}, CaCl{sub 2}, SrCl{sub 2} and FeCl{sub 3}, did not reduce dehydriding temperature of LiBH{sub 4} significantly. TGA-RGA analysis indicated that some halide modified lithium borohydrides such as LiBH{sub 4}+0.1ZnF{sub 2} evolved diborane during dehydrogenation, but some did not such as LiBH{sub 4}+0.1TiCl{sub 3}. The formation of diborane caused unrecoverable capacity loss resulting in irreversibility. It is suggested that the lithium borohydrides modified by the halides containing the metals that can not form metal borides with boron are likely to evolve diborane during dehydriding. It was discovered that halide modification reduces sensitivity of LiBH{sub 4}. The materials such as LiBH{sub 4}+0.1TiCl{sub 3} and LiBH{sub 4}+0.5TiCl{sub 3} can be handled in open air without visible reaction.

Au, M

2007-07-27T23:59:59.000Z

52

Methods for synthesizing alane without the formation of adducts and free of halides  

Science Conference Proceedings (OSTI)

A process is provided to synthesize an alane without the formation of alane adducts as a precursor. The resulting product is a crystallized .alpha.-alane and is a highly stable product and is free of halides.

Zidan, Ragaiy; Knight, Douglas A; Dinh, Long V

2013-02-19T23:59:59.000Z

53

Composite metal-hydrogen electrodes for metal-hydrogen batteries. Final report, October 1, 1993--April 15, 1997  

SciTech Connect

The purpose of this project is to develop and conduct a feasibility study of metallic thin films (multilayered and alloy composition) produced by advanced sputtering techniques for use as anodes in Ni-metal hydrogen batteries that would be deposited as distinct anode, electrolyte and cathode layers in thin film devices. The materials could also be incorporated in secondary consumer batteries (i.e. type AF(4/3 or 4/5)) which use electrodes in the form of tapes. The project was based on pioneering studies of hydrogen uptake by ultra-thin Pd-capped Nb films, these studies suggested that materials with metal-hydrogen ratios exceeding those of commercially available metal hydride materials and fast hydrogen charging and discharging kinetics could be produced. The project initially concentrated on gas phase and electrochemical studies of Pd-capped niobium films in laboratory-scale NiMH cells. This extended the pioneering work to the wet electrochemical environment of NiMH batteries and exploited advanced synchrotron radiation techniques not available during the earlier work to conduct in-situ studies of such materials during hydrogen charging and discharging. Although batteries with fast charging kinetics and hydrogen-metal ratios approaching unity could be fabricated, it was found that oxidation, cracking and corrosion in aqueous solutions made pure Nb films and multilayers poor candidates for battery application. The project emphasis shifted to alloy films based on known elemental materials used for NiMH batteries. Although commercial NiMH anode materials contain many metals, it was found that 0.24 {mu}m thick sputtered Zr-Ni films cycled at least 50 times with charging efficiencies exceeding 95% and [H]/[M] ratios of 0.7-1.0. Multilayered or thicker Zr-Ni films could be candidates for a thin film NiMH battery that may have practical applications as an integrated power source for modern electronic devices.

Ruckman, M.W.; Strongin, M.; Weismann, H. [and others

1997-04-01T23:59:59.000Z

54

Gas phase chromatography of halides of elements 104 and 105  

Science Conference Proceedings (OSTI)

On-line isothermal gas phase chromatography was used to study halides of {sup 261}104 (T{sub {1/2}} = 65 s) and {sup 262,263}105 (T{sub {1/2}} = 34 s and 27 s) produced an atom-at-a time via the reactions {sup 248}Cm({sup 18}O, 5n) and {sup 249}Bk({sup 18}O, 5n, 4n), respectively. Using HBr and HCl gas as halogenating agents, we were able to produce volatile bromides and chlorides of the above mentioned elements and study their behavior compared to their lighter homologs in Groups 4 or 5 of the periodic table. Element 104 formed more volatile bromides than its homolog Hf. In contrast, element 105 bromides were found to be less volatile than the bromides of the group 5 elements Nb and Ta. Both 104 and Hf chlorides were observed to be more volatile than their respective bromides. 31 refs., 8 figs.

Tuerler, A.; Gregorich, K.E.; Czerwinski, K.R.; Hannink, N.J.; Henderson, R.A.; Hoffman, D.C.; Kacher, C.D.; Kadkhodayan, B.; Kreek, S.A.; Lee, D.M.; Leyba, J.D.; Nurmia, M.J. (Lawrence Berkeley Lab., CA (United States)); Gaeggeler, H.W.; Jost, D.T.; Kovacs, J.; Scherer, U.W.; Vermeulen, D.; Weber, A. (Paul Scherrer Inst. (PSI), Villigen (Switzerland)); Barth, H.; Gober, M.K.; Kratz, J.V. (Philipps-Univ., Marburg

1991-04-01T23:59:59.000Z

55

Calcium Phosphate: A potential host for halide contaminated plutonium wastes.  

Science Conference Proceedings (OSTI)

The presence of significant quantities of fluoride and chloride in four types of legacy wastes from plutonium pyrochemical reprocessing required the development of a new wasteform which could adequately immobilize the halides in addition to the Pu and Am. Using a simulant chloride-based waste (Type I waste) and Sm as the surrogate for the Pu3+ and Am3+ present in the waste, AWE developed a process which utilised Ca3(PO4)2 as the host material. The waste was successfully incorporated into two crystalline phases, chlorapatite, [Ca5(PO4)3Cl], and spodiosite, [Ca2(PO4)Cl]. Radioactive studies performed at PNNL with 239Pu and 241Am confirmed the process. A slightly modified version of the process in which CaHPO4 was used as the host was successful in immobilizing a more complex multi-cation oxidebased waste (Type II) which contained significant concentrations of Cl and F in addition to 239Pu and 241Am. This waste resulted in the formation of cation-doped whitlockite, Ca3-xMgx(PO4)2, ?-calcium phosphate, ?-Ca2P2O7 and chlor-fluorapatite rather than the chlorapatite and spodiosite formed with Type I waste.

Metcalfe, Brian L.; Donald, Ian W.; Fong, Shirley K.; Gerrard, Lee A.; Strachan, Denis M.; Scheele, Randall D.

2009-07-06T23:59:59.000Z

56

DOE Science Showcase - Rare Earth Metal Research from DOE Databases |  

Office of Scientific and Technical Information (OSTI)

Rare Earth Metal Research from DOE Databases Rare Earth Metal Research from DOE Databases Information Bridge Energy Citations Database Highlighted documents of Rare Earth Metal research in DOE databases Information Bridge - Corrosion-resistant metal surfaces DOE R&D Project Summaries - Structural and magnetic studies on heavy rare earth metals at high pressures using designer diamonds Energy Citations Database - Intermultiplet transitions in rare-earth metals DOE Green Energy - LaNi.sub.5 is-based metal hydride electrode in Ni-MH rechargeable cells Science.gov - H.R.4866 - Rare Earths Supply-Chain Technology and Resources Transformation Act of 2010 WorldWideScience.org - China produces most of the world's rare earth metals DOepatents - Recycling of rare earth metals from rare earth-transition metal alloy scrap by liquid metal extraction

57

FUSED SALT METHOD FOR COATING URANIUM WITH A METAL  

DOE Patents (OSTI)

A method is presented for coating uranium with a less active metal such as Cr, Ni, or Cu comprising immersing the U in a substantially anhydrous molten solution of a halide of these less active metals in a ternary chloride composition which consists of selected percentages of KCl, NaCl and another chloride such as LiCl or CaCl/sub 2/.

Eubank, L.D.

1959-02-01T23:59:59.000Z

58

THE EFFECTS OF HALIDE MODIFIERS ON THE SORPTION KINETICS OF THE LI-MG-N-H SYSTEM  

DOE Green Energy (OSTI)

The effects of different transition metal halides (TiCl{sub 3}, VCl{sub 3}, ScCl{sub 3} and NiCl{sub 2}) on the sorption properties of the 1:1 molar ratio of LiNH{sub 2} to MgH{sub 2} are investigated. The modified mixtures were found to contain LiNH{sub 2}, MgH{sub 2} and LiCl. TGA results showed that the hydrogen desorption temperature was reduced with the modifier addition in this order: TiCl{sub 3} > ScCl{sub 3} > VCl{sub 3} > NiCL{sub 2}. Ammonia release was not significantly reduced resulting in a weight loss greater than the theoretical hydrogen storage capacity of the material. The isothermal sorption kinetics of the modified systems showed little improvement after the first dehydrogenation cycle over the unmodified system but showed drastic improvement in rehydrogenation cycles. X-ray diffraction and Raman spectroscopy identified the cycled material to be composed of LiH, MgH{sub 2}, Mg(NH{sub 2}){sub 2} and Mg{sub 3}N{sub 2}.

Anton, D.; Gray, J.; Price, C.; Lascola, R.

2011-07-20T23:59:59.000Z

59

THE AFFECTS OF HALIDE MODIFIERS ON THE SORPTION KINETICS OF THE LI-MG-N-H SYSTEM  

DOE Green Energy (OSTI)

In this present work, the affects of different transition metal halides (TiCl{sub 3}, VCl{sub 3}, ScCl{sub 3} and NiCl{sub 2}) on the sorption properties of the 1:1 molar ratio of LiNH{sub 2} to MgH{sub 2} are investigated. The modified mixtures were found to contain LiNH{sub 2}, MgH{sub 2} and LiCl. TGA results showed that the hydrogen desorption temperature was reduced with the modifier addition in this order: TiCl{sub 3}>ScCl{sub 3}>VCl{sub 3}>NiCl{sub 2}. Ammonia release was not significantly reduced resulting in a weight loss greater than the theoretical hydrogen storage capacity of the material. The isothermal sorption kinetics of the modified systems showed little improvement after the first dehydrogenation cycle over the unmodified system but showed drastic improvement in rehydrogenation cycles. XRD and Raman spectroscopy identified the cycled material to be composed of LiH, MgH{sub 2}, Mg(NH{sub 2}){sub 2} and Mg{sub 3}N{sub 2}.

Erdy, C.; Gray, J.; Lascola, R.; Anton, D.

2010-12-16T23:59:59.000Z

60

HANGER\MH  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

MASON & HANGER CORPORATION MASON & HANGER CORPORATION February 10, 1998 U. S. Department of Energy Office of General Counsel, GC-52 1000 Independence Ave. SW. Washington, DC 20585 Subject: Reply comments to notice of inquiry concerning preparation of report to Congress on the Price-Anderson Act Dear Sir or Madam: Mason & Hanger Corporation has reviewed the Federal Register Notice published December 31, 1997. It is our intent to offer the attached replies to the listed questions contained in the Notice. Thank you for the opportunity to provide input to the report preparation process. Please contact myself or Alan G. Wagner, Esq. at (806) 477-7233 if you have any questions. Very truly yours,

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

Extraction of trace metals from fly ash  

DOE Patents (OSTI)

A process for recovering silver, gallium and/or other trace metals from a fine grained industrial fly ash associated with a process for producing phosphorous, the fly ash having a silicate base and containing surface deposits of the trace metals as oxides, chlorides or the like, with the process being carried out by contacting the fly ash with AlCl.sub.3 in an alkali halide melt to react the trace metals with the AlCl.sub.3 to form compositions soluble in the melt and a residue containing the silicate and aluminum oxide or other aluminum precipitate, and separating the desired trace metal or metals from the melt by electrolysis or other separation techniques.

Blander, Milton (Palos Park, IL); Wai, Chien M. (Moscow, ID); Nagy, Zoltan (Woodridge, IL)

1984-01-01T23:59:59.000Z

62

Extraction of trace metals from fly ash  

DOE Patents (OSTI)

A process is described for recovering silver, gallium and/or other trace metals from a fine grained industrial fly ash associated with a process for producing phosphorous. The fly ash has a silicate base and contains surface deposits of the trace metals as oxides, chlorides or the like. The process is carried out by contacting the fly ash with AlCl/sub 3/ in an alkali halide melt to react the trace metals with the AlCl/sub 3/ to form compositions soluble in the melt and a residue containing the silicate and aluminum oxide or other aluminum precipitate, and separating the desired trace metal or metals from the melt by electrolysis or other separation techniques.

Blander, M.; Wai, C.M.; Nagy, Z.

1983-08-15T23:59:59.000Z

63

Studies on a novel secondary battery: MH/MnO{sub 2} rechargeable battery. 2: Characteristics of the MnO{sub 2} cathode  

SciTech Connect

The characteristics of the MnO{sub 2} cathode of a MH/MnO{sub 2} battery have been studied by cyclic voltammetry, x-ray diffraction, and potentiostatic techniques. It was found that the addition of Ni(OH){sub 2} to the MnO{sub 2} can prevent overcharge of the MnO{sub 2} and decrease the imbalance of the charge/discharge states of the positive and negative electrodes, raise the working voltage of the MH/MnO{sub 2} cell, and prevent the formation of Mn{sub 3}O{sub 4}, thereby improving the rechargeability of the MnO{sub 2} electrode. The discharge mechanism is also discussed.

Xia, X.; Guo, Z. [Xinjiang Univ., Urumqi, Xinjiang (China). Dept. of Chemistry

1997-08-01T23:59:59.000Z

64

Self-discharge mechanism of sealed-type nickel/metal-hydride battery  

Science Conference Proceedings (OSTI)

Factors affecting the self-discharge rate of a nickel/metal-hydride (Ni-MH) battery, generally much higher than that of nickel/cadmium (Ni-Cd) battery, are investigated, and the self-discharge mechanism is discussed. Ammonia and amine participate in the shuttle reaction like nitrate ion in the Ni-Cd battery, resulting in acceleration of the self-discharge. When nonwoven fabric made of sulfonated-polypropylene is used as a separator instead of conventional polyamide separator, the self-discharge rate of the Ni-MH battery is strongly depressed, to the same level as that of Ni-Cd battery.

Ikoma, Munehisa; Hoshina, Yasuko; Matsumoto, Isao [Matsushita Battery Industrial Co., Ltd., Osaka (Japan); Iwakura, Chiaki [Univ. of Osaka Prefecture, Sakai, Osaka (Japan). Dept. of Applied Chemistry

1996-06-01T23:59:59.000Z

65

Investigation into Nanostructured Lanthanum Halides and CeBr{sub 3} for Nuclear Radiation Detection  

Science Conference Proceedings (OSTI)

This slide-show presents work on radiation detection with nanostructured lanthanum halides and CeBr{sub 3}. The goal is to extend the gamma energy response on both low and high-energy regimes by demonstrating the ability to detect low-energy x-rays and relatively high-energy activation prompt gamma rays simultaneously using the nano-structured lanthanum bromide, lanthanum fluoride, cerium bromide, or other nanocrystal material. Homogeneous and nano structure cases are compared.

Guss, P., Guise, R., Mukhopadhyay, S., Yuan, D.

2011-06-22T23:59:59.000Z

66

Liquid suspensions of reversible metal hydrides  

DOE Patents (OSTI)

The reversibility of the process M + x/2 H/sub 2/ ..-->.. MH/sub x/, where M is a metal hydride former that forms a hydride MH/sub x/ in the presence of H/sub 2/, generally used to store and recall H/sub 2/, is found to proceed under a liquid, thereby to reduce contamination, provide better temperature control and provide in situ mobility of the reactants. Thus, a slurry of particles of a metal hydride former with an inert solvent is subjected to temperature and pressure controlled atmosphere containing H/sub 2/, to store hydrogen (at high pressures) and to release (at low pressures) previously stored hydrogen. The direction of the flow of the H/sub 2/ through the liquid is dependent upon the H/sub 2/ pressure in the gas phase at a given temperature. When the former is above the equilibrium absorption pressure of the respective hydride the reaction proceeds to the right, i.e., the metal hydride is formed and hydrogen is stored in the solid particle. When the H/sub 2/ pressure in the gas phase is below the equilibrium dissociation pressure of the respective hydride the reaction proceeds to the left, the metal hydride is decomposed and hydrogen is released into the gas phase.

Reilly, J.J.; Grohse, E.W.; Winsche, W.E.

1983-12-08T23:59:59.000Z

67

Current status of environmental, health, and safety issues of nickel metal-hydride batteries for electric vehicles  

Science Conference Proceedings (OSTI)

This report identifies important environment, health, and safety issues associated with nickel metal-hydride (Ni-MH) batteries and assesses the need for further testing and analysis. Among the issues discussed are cell and battery safety, workplace health and safety, shipping requirements, and in-vehicle safety. The manufacture and recycling of Ni-MH batteries are also examined. This report also overviews the ``FH&S`` issues associated with other nickel-based electric vehicle batteries; it examines venting characteristics, toxicity of battery materials, and the status of spent batteries as a hazardous waste.

Corbus, D.; Hammel, C.J.; Mark, J.

1993-08-01T23:59:59.000Z

68

Method of removal of heavy metal from molten salt in IFR fuel pyroprocessing  

DOE Patents (OSTI)

An electrochemical method of separating heavy metal values from a radioactive molten salt including Li halide at temperatures of about 500{degree}C. The method comprises positioning a solid Li-Cd alloy anode in the molten salt containing the heavy metal values, positioning a Cd-containing cathode or a solid cathode positioned above a catch crucible in the molten salt to recover the heavy metal values, establishing a voltage drop between the anode and the cathode to deposit material at the cathode to reduce the concentration of heavy metals in the salt, and controlling the deposition rate at the cathode by controlling the current between the anode and cathode.

Gay, E.C.

1993-12-23T23:59:59.000Z

69

Method of removal of heavy metal from molten salt in IFR fuel pyroprocessing  

DOE Patents (OSTI)

An electrochemical method of separating heavy metal values from a radioactive molten salt including Li halide at temperatures of about 500.degree. C. The method comprises positioning a solid Li--Cd alloy anode in the molten salt containing the heavy metal values, positioning a Cd-containing cathode or a solid cathode positioned above a catch crucible in the molten salt to recover the heavy metal values, establishing a voltage drop between the anode and the cathode to deposit material at the cathode to reduce the concentration of heavy metals in the salt, and controlling the deposition rate at the cathode by controlling the current between the anode and cathode.

Gay, Eddie C. (Park Forest, IL)

1995-01-01T23:59:59.000Z

70

Nickel-metal hydride battery development. Final technical report  

SciTech Connect

Rechargeable batteries are used as the power source for a broad range of portable equipment. Key battery selection criteria typically are weight, volume, first cost, life cycle cost, and environmental impact. Rechargeable batteries are favored from a life cycle cost and environmental impact standpoint over primary batteries. The nickel-metal hydride (Ni-MH) battery system has emerged as the battery of choice for many applications based on its superior characteristics when judged on the above criteria against other battery types. In most cases commercial Ni-MH batteries are constructed with coiled electrodes in cylindrical metal containers. Electro Energy, Inc. (EEI) has been developing a novel flat bipolar configuration of the Ni-MH system that offers weight, volume, and cost advantages when compared to cylindrical cells. The unique bipolar approach consists of fabricating individual flat wafer cells in conductive, carbon-filled, plastic face plates. The individual cells contain a nonconductive plastic border which is heat sealed around the perimeter to make a totally sealed unit cell. Multi-cell batteries are fabricated by stacking the individual wafer cells in such a way that the positive face of one cell contacts the negative face of the adjacent cell. The stack is then contained in an outer housing with end contacts. The purpose of this program was to develop, evaluate, and demonstrate the capabilities of the EEI Ni-MH battery system for consumer applications. The work was directed at the development and evaluation of the compact bipolar construction for its potential advantages of high power and energy density. Experimental investigations were performed on various nickel electrode types, hydride electrode formulations, and alternate separator materials. Studies were also directed at evaluating various oxygen recombination techniques for low pressure operation during charge and overcharge.

1995-06-01T23:59:59.000Z

71

Method for dry etching of transition metals  

DOE Patents (OSTI)

A method for dry etching of transition metals. The method for dry etching of a transition metal (or a transition metal alloy such as a silicide) on a substrate comprises providing at least one nitrogen- or phosphorous-containing .pi.-acceptor ligand in proximity to the transition metal, and etching the transition metal to form a volatile transition metal/.pi.-acceptor ligand complex. The dry etching may be performed in a plasma etching system such as a reactive ion etching (RIE) system, a downstream plasma etching system (i.e. a plasma afterglow), a chemically-assisted ion beam etching (CAIBE) system or the like. The dry etching may also be performed by generating the .pi.-acceptor ligands directly from a ligand source gas (e.g. nitrosyl ligands generated from nitric oxide), or from contact with energized particles such as photons, electrons, ions, atoms, or molecules. In some preferred embodiments of the present invention, an intermediary reactant species such as carbonyl or a halide ligand is used for an initial chemical reaction with the transition metal, with the intermediary reactant species being replaced at least in part by the .pi.-acceptor ligand for forming the volatile transition metal/.pi.-acceptor ligand complex.

Ashby, Carol I. H. (Edgewood, NM); Baca, Albert G. (Albuquerque, NM); Esherick, Peter (Albuquerque, NM); Parmeter, John E. (Albuquerque, NM); Rieger, Dennis J. (Tijeras, NM); Shul, Randy J. (Albuquerque, NM)

1998-01-01T23:59:59.000Z

72

Method for dry etching of transition metals  

DOE Patents (OSTI)

A method for dry etching of transition metals is disclosed. The method for dry etching of a transition metal (or a transition metal alloy such as a silicide) on a substrate comprises providing at least one nitrogen- or phosphorus-containing {pi}-acceptor ligand in proximity to the transition metal, and etching the transition metal to form a volatile transition metal/{pi}-acceptor ligand complex. The dry etching may be performed in a plasma etching system such as a reactive ion etching (RIE) system, a downstream plasma etching system (i.e. a plasma afterglow), a chemically-assisted ion beam etching (CAIBE) system or the like. The dry etching may also be performed by generating the {pi}-acceptor ligands directly from a ligand source gas (e.g. nitrosyl ligands generated from nitric oxide), or from contact with energized particles such as photons, electrons, ions, atoms, or molecules. In some preferred embodiments of the present invention, an intermediary reactant species such as carbonyl or a halide ligand is used for an initial chemical reaction with the transition metal, with the intermediary reactant species being replaced at least in part by the {pi}-acceptor ligand for forming the volatile transition metal/{pi}-acceptor ligand complex.

Ashby, C.I.H.; Baca, A.G.; Esherick, P.; Parmeter, J.E.; Rieger, D.J.; Shul, R.J.

1998-09-29T23:59:59.000Z

73

J. Am. Chem. SOC.1991, 113,9575-9585 9575 Mixed Aggregation of Lithium Enolates and Lithium Halides  

E-Print Network (OSTI)

J. Am. Chem. SOC.1991, 113,9575-9585 9575 Mixed Aggregation of Lithium Enolates and Lithium Halides with Lithium 2,2,6,6-Tetramethylpiperidide(LiTMP) Patricia L. Hall, James H. Gilchrist, Aidan T. Harrison]-lithiumdi-tert-butylamide and conformationally locked [6Li]-lithium2,2,4,6,6-pentamethylpiperidide shed further light

Collum, David B.

74

Metal Aminoboranes  

Metal aminoboranes of the formula M(NH.sub.2BH.sub.3).sub.n have been synthesized. Metal aminoboranes are hydrogen storage materials. Metal aminoboranes are also precursors for synthesizing other metal aminoboranes. Metal aminoboranes can be ...

75

High Permeability Ternary Palladium Alloy Membranes with Improved Sulfur and Halide Tolerance  

NLE Websites -- All DOE Office Websites (Extended Search)

9 9 HigH Permeability ternary Palladium alloy membranes witH imProved sulfur and Halide tolerance Description A critical step in the transition to the hydrogen economy is the separation of hydrogen from coal gasification gases (syngas) or methane. This is typically accomplished through membrane separation. Past research has shown that palladium (Pd) alloys possess great potential as robust and economical membranes. However, the search for the optimal binary or ternary alloys is an involved and costly process due to the immense number of alloy variations that could be prepared and tested. Recent modeling work at Georgia Institute of Technology using density functional theory (DFT) identified several promising ternary alloy compositions with improved

76

Studies of non-proportionality in alkali halide and strontium iodide scintillators using SLYNCI  

Science Conference Proceedings (OSTI)

Recently a collaboration of LLNL and LBNL has constructed a second generation Compton coincidence instrument to study the non-proportionality of scintillators. This device, known as SLYNCI (Scintillator Light-Yield Non-proportionality Characterization Instrument), has can completely characterize a sample with less than 24 hours of running time. Thus, SLYNCI enables a number of systematic studies of scintillators since many samples can be processed in a reasonable length of time. These studies include differences in nonproportionality between different types of scintillators, different members of the same family of scintillators, and impact of different doping levels. The results of such recent studies are presented here, including a study of various alkali halides, and the impact of europium doping level in strontium iodide. Directions of future work area also discussed.

Ahle, Larry; Bizarri, Gregory; Boatner, Lynn; Cherepy, Nerine J.; Choong, Woon-Seng; Moses, William W.; Payne, Stephen A.; Shah, Kanai; Sheets, Steven; Sturm, Benjamin, W.

2010-10-14T23:59:59.000Z

77

Studies of Non-Proportionality in Alkali Halide and Strontium Iodide Scintillators Using SLYNCI  

Science Conference Proceedings (OSTI)

Recently a collaboration of LLNL and LBNL has constructed a second generation Compton coincidence instrument to study the non-proportionality of scintillators [1-3]. This device, known as SLYNCI (Scintillator Light-Yield Non-proportionality Characterization Instrument), has can completely characterize a sample with less than 24 hours of running time. Thus, SLYNCI enables a number of systematic studies of scintillators since many samples can be processed in a reasonable length of time. These studies include differences in nonproportionality between different types of scintillators, different members of the same family of scintillators, and impact of different doping levels. The results of such recent studies are presented here, including a study of various alkali halides, and the impact of europium doping level in strontium iodide. Directions of future work area also discussed.

Ahle, L; Bizarri, G; Boatner, L; Cherepy, N J; Choong, W; Moses, W W; Payne, S A; Shah, K; Sheets, S; Sturm, B W

2009-05-05T23:59:59.000Z

78

Ambient-temperature superconductor symetrical metal-dihalide bis-(ethylenedithio)-tetrathiafulvalene compounds  

DOE Patents (OSTI)

A new class of organic superconductors having the formula (ET).sub.2 MX.sub.2 wherein ET represents bis(ethylenedithio)-tetrathiafulvalene, M is a metal such as Au, Ag, In, Tl, Rb, Pd and the like and X is a halide. The superconductor (ET).sub.2 AuI.sub.2 exhibits a transition temperature of 5 K. which is high for organic superconductors.

Williams, Jack M. (Downers Grove, IL); Wang, Hsien-Hau (Willowbrook, IL); Beno, Mark A. (Woodridge, IL)

1987-01-01T23:59:59.000Z

79

Persistent infrared spectral hole burning of NO; ions in potassium halide crystals. I. Priric9ple and satellite.holle generation  

E-Print Network (OSTI)

Persistent infrared spectral hole burning of NO; ions in potassium halide crystals. I. Priric9ple spectroscopyand persistentinfrared spectralhole (PIRSH) burning separatelyand together. With interferometry cm --'and, with PIRSH burning, it has beendemijnstratedthat the narrowestlinesare

Sethna, James P.

80

Nanostructured Lanthanum Halides and CeBr3 for Nuclear Radiation and Detection  

Science Conference Proceedings (OSTI)

Scintillator materials are used to detect, and in some cases identify, gamma rays. Higher performance scintillators are expensive, hard to manufacture, fragile, and sometimes require liquid nitrogen or cooling engines. But whereas lower-quality scintillators are cheap, easy to manufacture, and more rugged, their performance is lower. At issue: can the desirable qualities of high-and low-performance scintillators be combined to achieve better performance at lower cost? Preliminary experiments show that a LaF{sub 3}:Ce oleic acid-based nanocomposite exhibits a photopeak when exposed to {sup 137}Cs source gamma-radiation. The chemical synthesis of the cerium-doped lanthanum halide nanoparticles are scalable and large quantities of material can be produced at a time, unlike typical crystal growth processes such as the Bridgeman process. Using a polymer composite (Figure 1), produced by LANL, initial measurements of the unloaded and 8% LaF{sub 3}:Ce-loaded sample have been made using {sup 137}Cs sources. Figure 2 shows an energy spectrum acquired for CeF{sub 3}. The lighter plot is the measured polymer-only spectrum and the black plot is the spectrum from the nanocomposite scintillator. As the development of this material continues, the energy resolution is expected to improve and the photopeak-to-Compton ratio will become greater at higher loadings. These measurements show the expected Compton edge in the polymer-only sample, and the Compton edge and photo-peak expected in the nanophosphor composites that LANL has produced. Using a porous VYCORR with CdSe/ZnS core shell quantum dots, Letant has demonstrated that he has obtained signatures of the 241Am photopeak with energy resolution as good at NaI (Figure 3). We begin with the fact that CeBr{sub 3} crystals do not have a self-activity component as strong as the lanthanum halides. The radioactive 0.090% {sup 138}La component of lanthanum leads to significant self-activity, which will be a problem for very large detector volumes. Yet a significant strength of the nanostructure detector concept is the ability to create extremely large detector volumes by mixing nanoparticles into a transparent matrix. This would argue for use of nanoparticles other than lanthanum halides. Nanocomposites are easy to prepare; it is much less costly to use nanocomposites than to grow large whole crystals of these materials. The material can be fabricated at an industrial scale, further reducing cost. This material potentially offers the performance of $300/cc material (e.g., lanthanum bromide) at a cost of $1/cc. Because the material acts as a plastic, it is rugged and flexible, and can be made in large sheets, increasing the sensitivity of a detector using it. It would operate at ambient temperatures. Very large volumes of detector may be produced at greatly reduced cost, enhancing the non-proliferation posture of the nation for the same dollar value.

Paul Guss, Sanjoy Mukhopadhyay, Ron Guise, Ding Yuan

2010-06-09T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Calcium looping process for high purity hydrogen production integrated with capture of carbon dioxide, sulfur and halides  

DOE Patents (OSTI)

A process for producing hydrogen comprising the steps of: (i) gasifying a fuel into a raw synthesis gas comprising CO, hydrogen, steam, sulfur and halide contaminants in the form of H.sub.2S, COS, and HX, wherein X is a halide; (ii) passing the raw synthesis gas through a water gas shift reactor (WGSR) into which CaO and steam are injected, the CaO reacting with the shifted gas to remove CO.sub.2, sulfur and halides in a solid-phase calcium-containing product comprising CaCO.sub.3, CaS and CaX.sub.2; (iii) separating the solid-phase calcium-containing product from an enriched gaseous hydrogen product; and (iv) regenerating the CaO by calcining the solid-phase calcium-containing product at a condition selected from the group consisting of: in the presence of steam, in the presence of CO.sub.2, in the presence of synthesis gas, in the presence of H.sub.2 and O.sub.2, under partial vacuum, and combinations thereof.

Ramkumar, Shwetha; Fan, Liang-Shih

2013-07-30T23:59:59.000Z

82

Metal Aminoboranes  

NLE Websites -- All DOE Office Websites (Extended Search)

Metal Aminoboranes Metal Aminoboranes Metal Aminoboranes Metal aminoboranes of the formula M(NH.sub.2BH.sub.3).sub.n have been synthesized. June 25, 2013 Metal Aminoboranes Metal aminoboranes of the formula M(NH.sub.2BH.sub.3).sub.n have been synthesized. Available for thumbnail of Feynman Center (505) 665-9090 Email Metal Aminoboranes Metal aminoboranes of the formula M(NH.sub.2BH.sub.3).sub.n have been synthesized. Metal aminoboranes are hydrogen storage materials. Metal aminoboranes are also precursors for synthesizing other metal aminoboranes. Metal aminoboranes can be dehydrogenated to form hydrogen and a reaction product. The reaction product can react with hydrogen to form a hydrogen storage material. Metal aminoboranes can be included in a kit. U.S. Patent No.: 7,713,506 (DOE S-112,798)

83

Progress in the development of Ovonic nickel-metal hydride batteries  

SciTech Connect

Proprietary, multicomponent hydrogen storage alloys using the principles of atomic engineering form the heart of Ovonic Nickel-Metal Hydride (Ni/MH) battery technology. This battery system, in development for 10 years, has been licensed to several manufacturers both for consumer cells and electric vehicle batteries. These cells have achieved a specific energy of over 80 Wh/kg, a peak power in excess of 200 W/kg, and over 1000 cycles at 100% depth of discharge. They also have an intrinsic ability to withstand overcharge and overdischarge abuse. Ovonic Ni/MH batteries are environmentally friendly and can be recycled. Performance data will be presented showing the successful scale-up of this technology for electric vehicle applications.

Venkatesan, S.; Corrigan, D.A.; Gifford, P.R.; Fetcenko, M.A.; Dhar, S.K.; Ovshinsky, S.R. (Ovonic Battery Co., Troy, MI (United States))

1993-05-01T23:59:59.000Z

84

Synthesis of Cyclic Aza-Ether Compounds and Studies of Their Use as Anion Receptors in Non-Aqueous Lithium Halide Salt Solutions  

DOE Green Energy (OSTI)

A series of new anion receptors, based on cyclic aza-ether compounds, have been synthesized. In all of these cyclic aza-ether compounds, the electron-withdrawing group CF{sub 3}SO{sub 2} was attached to each of the nitrogen atoms. When used as additives, all of them can significantly increase the ionic conductivity of lithium halide salts in THF solutions. This is due to the complexation between these compounds and halide anions. Ionic conductivity studies show that the complexation behavior is related to both the ring structure of the cyclic compounds and the characteristics of the halide anions. X-ray diffraction data show that the diffraction patterns of the complex crystals are different from the pure cyclic aza-ether compounds. New Bragg peaks representing a large d-spacing ({approx}15 {angstrom}) are observed for the complex crystals which provides a clear evidence for complexation.

Lee, H. S.; Sun, X.; Yang, X. Q.; McBreen, J.; Callahan, J. H.; Choi, L. S.

1999-11-01T23:59:59.000Z

85

Gas Phase Chromatography of some Group 4, 5, and 6 Halides  

Science Conference Proceedings (OSTI)

Gas phase chromatography using The Heavy Element Volatility Instrument (HEVI) and the On Line Gas Apparatus (OLGA III) was used to determine volatilities of ZrBr{sub 4}, HfBr{sub 4}, RfBr{sub 4}, NbBr{sub 5}, TaOBr{sub 3}, HaCl{sub 5}, WBr{sub 6}, FrBr, and BiBr{sub 3}. Short-lived isotopes of Zr, Hf, Rf, Nb, Ta, Ha, W, and Bi were produced via compound nucleus reactions at the 88-Inch Cyclotron at Lawrence Berkeley National Laboratory and transported to the experimental apparatus using a He gas transport system. The isotopes were halogenated, separated from the other reaction products, and their volatilities determined by isothermal gas phase chromatography. Adsorption Enthalpy ({Delta}H{sub a}) values for these compounds were calculated using a Monte Carlo simulation program modeling the gas phase chromatography column. All bromides showed lower volatility than molecules of similar molecular structures formed as chlorides, but followed similar trends by central element. Tantalum was observed to form the oxybromide, analogous to the formation of the oxychloride under the same conditions. For the group 4 elements, the following order in volatility and {Delta}H{sub a} was observed: RfBr{sub 4} > ZrBr{sub 4} > HfBr{sub 4}. The {Delta}H{sub a} values determined for the group 4, 5, and 6 halides are in general agreement with other experimental data and theoretical predictions. Preliminary experiments were performed on Me-bromides. A new measurement of the half-life of {sup 261}Rf was performed. {sup 261}Rf was produced via the {sup 248}Cm({sup 18}O, 5n) reaction and observed with a half-life of 74{sub -6}{sup +7} seconds, in excellent agreement with the previous measurement of 78{sub -6}{sup +11} seconds. We recommend a new half-life of 75{+-}7 seconds for {sup 261}Rf based on these two measurements. Preliminary studies in transforming HEVI from an isothermal (constant temperature) gas phase chromatography instrument to a thermochromatographic (variable temperature) instrument have been completed. Thermochromatography is a technique that can be used to study the volatility and {Delta}H{sub a} of longer-lived isotopes off-line, Future work will include a comparison between the two techniques and the use of thermochromatography to study isotopes in a wider range of half-lives and molecular structures.

Sylwester, Eric Robert

1998-10-01T23:59:59.000Z

86

The Open Cluster Chemical Analysis and Mapping Survey: Local Galactic Metallicity Gradient with APOGEE using SDSS DR10  

E-Print Network (OSTI)

The Open Cluster Chemical Analysis and Mapping (OCCAM) Survey aims to produce a comprehensive, uniform, infrared-based dataset for hundreds of open clusters, and constrain key Galactic dynamical and chemical parameters from this sample. This first contribution from the OCCAM survey presents analysis of 141 members stars in 28 open clusters with high-resolution metallicities derived from a large uniform sample collected as part of the SDSS-III/Apache Point Observatory Galactic Evolution Experiment (APOGEE). This sample includes the first high-resolution metallicity measurements for 22 open clusters. With this largest ever uniformly observed sample of open cluster stars we investigate the Galactic disk gradients of both [M/H] and [alpha/M]. We find basically no gradient across this range in [alpha/M], but [M/H] does show a gradient for R_{GC} < 10 kpc and a significant flattening beyond R_{GC} = 10 kpc. In particular, whereas fitting a single linear trend yields an [M/H] gradient of -0.09 +/- 0.03$ dex/kpc -...

Frinchaboy, Peter M; Jackson, Kelly M; O'Connell, Julia; Meyer, Brianne; Zasowski, Gail; Majewski, Steven R; Chojnowksi, S Drew; Johnson, Jennifer A; Prieto, Carlos Allende; Beers, Timothy C; Bizyaev, Dmitry; Brewington, Howard; Cunha, Katia; Ebelke, Garrett; Perez, Ana Elia Garcia; Hearty, Frederick R; Holtzman, Jon; Kinemuchi, Karen; Malanushenko, Elena; Malanushenko, Viktor; Marchante, Moses; Meszaros, Szabolcs; Muna, Demitri; Nidever, David L; Oravetz, Daniel; Pan, Kaike; Schiavon, Ricardo P; Schneider, Donald P; Shetrone, Matthew; Simmons, Audrey; Snedden, Stephanie; Smith, Verne V; Wilson, John C

2013-01-01T23:59:59.000Z

87

Light Metals  

Science Conference Proceedings (OSTI)

Alternative processes; Anode design and operation; Cell fundamentals and ... Hot-rolling technologies; Deformation of materials; Primary metal production.

88

Method of removal of heavy metal from molten salt in IFR fuel pyroprocessing  

DOE Patents (OSTI)

An electrochemical method is described for separating heavy metal values from a radioactive molten salt including Li halide at temperatures of about 500 C. The method comprises positioning a solid Li--Cd alloy anode in the molten salt containing the heavy metal values, positioning a Cd-containing cathode or a solid cathode positioned above a catch crucible in the molten salt to recover the heavy metal values, establishing a voltage drop between the anode and the cathode to deposit material at the cathode to reduce the concentration of heavy metals in the salt, and controlling the deposition rate at the cathode by controlling the current between the anode and cathode. 3 figs.

Gay, E.C.

1995-10-03T23:59:59.000Z

89

The effects of halides on the performance of coal gas-fueled molten carbonate fuel cells: Final report, October 1986-October 1987  

DOE Green Energy (OSTI)

This report presents the results of a program to determine the probable tolerable limits of hydrogen chloride and hydrogen fluoride present in the fuel and oxidant streams of molten carbonate fuel cells that are operating on gasified coal. A literature survey and thermodynamic analyses were performed to determine the likely effects of halides on cell performance and materials. Based on the results of these studies, accelerated corrosion experiments and electrode half-cell performance tests were conducted using electrolyte which contained chloride and fluoride. These data and the results of previous in-cell tests were used to develop a computer for predicting the performance decay due to these halides. The tolerable limits were found to be low (less than 1 PPM) and depend on the power plant system configuration, the operating conditions of the fuel cell stack, the cell design and initial electrolyte inventory, and the ability of the cell to scrub low levels of halide from the reactant streams. The primary decay modes were conversion of the electrolyte from pure carbonate to a carbonate-halide mixture and accelerated electrolyte evaporation. 75 figs., 16 tabs.

Magee, T.P.; Kunz, H.R.; Krasij, M.; Cote, H.A.

1987-10-01T23:59:59.000Z

90

Halide, Chromate, and Phosphate Impacts on LAW Glass for Dynamic Flowsheet 24590-WTP-MCR-PET-09-0037, Rev. 1  

SciTech Connect

Revision 1 of this Model Change Request changed Equation 6 in Attachment Al only. Melter studies have shown that halide, chromium, and phosphates can cause precipitation of solids that can interfer the melting process. Pilot melter data now shows what concentrations LAW glass can tolerate. These limits shall be incorporated into the existing LAW glass algorithm per Attachment Al.

Gimpel, Rodney F.; Kruger, Albert A.

2013-12-16T23:59:59.000Z

91

Plutonium metal preparation and purification at Los Alamos, 1984  

Science Conference Proceedings (OSTI)

Plutonium metal preparation and purification are well established at Los Alamos. Metal is prepared by calcothermic reduction of both PuF/sub 4/ and PuO/sub 2/. Metal is purified by halide slagging, casting, and electrorefining. The product from the production sequence is ultrapure plutonium metal. All of the processes involve high temperature operation and all but casting involve molten salt media. Development efforts are fourfold: (1) recover plutonium values from residues; (2) reduce residue generation through process improvements and changes; (3) recycle of reagents, and (4) optimize and integrate all processes into a close-loop system. Plutonium residues are comprised of oxides, chlorides, colloidal metal suspensions, and impure metal heels. Pyrochemical recovery techniques are under development to address each residue. In addition, we are looking back at each residue generation step and are making process changes to reduce plutonium content in each residue. Reagent salt is the principle media used in pyrochemical processing. The regeneration and recycle of these reagents will both reduce our waste handling and operating expense. The fourth area, process optimization, involves both existing processes and new process developments. A status of efforts in all four of these areas will be summarized.

Christensen, D.C.; Williams, J.D.; McNeese, J.A.; Fife, K.W.

1984-01-01T23:59:59.000Z

92

Versatile 0. 5 TW electron beam facility for power conditioning studies of large rare-gas/halide lasers  

Science Conference Proceedings (OSTI)

Rare-gas/halide lasers which are being developed for Inertial Confinement Fusion will require large area, low impedance electron beam drivers. A wide range of electron beam parameters are being considered for future systems in an effort to optimize the overall system design. A number of power conditioning issues must be investigated in order to obtain a better understanding of the various trade-offs involved in making such optimizations. The RAYITO electron beam accelerator is being designed and built at Sandia National Laboratories and will be used for such investigations. It will be capable of operating in either a 2 or 4 ohm configuration at 1 MV, 50 ns or 0.8 MV, 200 ns. Design details for RAYITO are presented in this paper. Experiments planned for this facility are also discussed.

Ramirez, J. J.

1980-01-01T23:59:59.000Z

93

Studies of Non-Proportionality in Alkali Halide and Strontium Iodide Scintillators Using SLYNCI 6-16-2009  

Science Conference Proceedings (OSTI)

Recently a collaboration of LLNL and LBNL has constructed a second generation Compton coincidence instrument to study the non-proportionality of scintillators. This device, known as SLYNCI (Scintillator Light-Yield Non-proportionality Characterization Instrument), has can completely characterize a sample with less than 24 hours of running time. Thus, SLYNCI enables a number of systematic studies of scintillators since many samples can be processed in a reasonable length of time. These studies include differences in non-proportionality between different types of scintillators, different members of the same family of scintillators, and impact of different doping levels. The results of such recent studies are presented here, including a study of various alkali halides, and the impact of europium doping level in strontium iodide. Directions of future work area also discussed.

Ahle, Larry [Lawrence Livermore National Laboratory (LLNL); Bizarri, Gregory [Lawrence Berkeley National Laboratory (LBNL); Boatner, Lynn A [ORNL; Cherepy, Nerine [Lawrence Livermore National Laboratory (LLNL); Choong, Woon-Seng [Lawrence Berkeley National Laboratory (LBNL); Moses, W. W. [Lawrence Berkeley National Laboratory (LBNL); Payne, Stephen A. [Lawrence Livermore National Laboratory (LLNL); Shah, Kanai [Radiation Monitoring Devices, Watertown, MA; Sheets, Steven [Lawrence Livermore National Laboratory (LLNL); Sturm, Benjamin [Lawrence Livermore National Laboratory (LLNL)

2009-01-01T23:59:59.000Z

94

Precious Metals  

Science Conference Proceedings (OSTI)

"Advances in the Extractive Metallurgy of Selected Rare and Precious Metals" ( 1991 Review of Extractive Metallurgy), J.E. Hoffmann, April 1991, pp. 18-23.

95

Integrated DWPF Melter System (IDMS) campaign report: The first two noble metals operations  

DOE Green Energy (OSTI)

The Integrated DWPF Melter System (IDMS) is designed and constructed to provide an engineering-scale representation of the DWPF melter and its associated feed preparation and off-gas systems. The facility is the first pilot-scale melter system capable of processing mercury, and flowsheet levels of halides and noble metals. In order to characterize the processing of noble metals (Pd, Rh, Ru, and Ag) on a large scale, the IDMS will be operated batchstyle for at least nine feed preparation cycles. The first two of these operations are complete. The major observation to date occurred during the second run when significant amounts of hydrogen were evolved during the feed preparation cycle. The runs were conducted between June 7, 1990 and March 8, 1991. This time period included nearly six months of ``fix-up`` time when forced air purges were installed on the SRAT MFT and other feed preparation vessels to allow continued noble metals experimentation.

Hutson, N.D.; Zamecnik, J.R.; Smith, M.E.; Miller, D.H.; Ritter, J.A.

1991-06-06T23:59:59.000Z

96

Process for forming epitaxial perovskite thin film layers using halide precursors  

DOE Patents (OSTI)

A process for forming an epitaxial perovskite-phase thin film on a substrate. This thin film can act as a buffer layer between a Ni substrate and a YBa.sub.2 Cu.sub.3 O.sub.7-x superconductor layer. The process utilizes alkali or alkaline metal acetates dissolved in halogenated organic acid along with titanium isopropoxide to dip or spin-coat the substrate which is then heated to about 700.degree. C. in an inert gas atmosphere to form the epitaxial film on the substrate. The YBCO superconductor can then be deposited on the layer formed by this invention.

Clem, Paul G. (Albuquerque, NM); Rodriguez, Mark A. (Albuquerque, NM); Voigt, James A. (Corrales, NM); Ashley, Carol S. (Albuquerque, NM)

2001-01-01T23:59:59.000Z

97

BEFORE THE U.S. DEPARTMENT OF ENERGY  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

I, 2009, each metal halide lamp fixture with a magnetic probe-start metal halide ballast must contain a magnetic probe-start metal halide ballast with a minimum ballast...

98

Dry halide method for separating the components of spent nuclear fuels  

DOE Patents (OSTI)

The invention is a nonaqueous, single method for processing multiple spent nuclear fuel types by separating the fission- and transuranic products from the nonradioactive and fissile uranium product. The invention has four major operations: exposing the spent fuels to chlorine gas at temperatures preferably greater than 1200.degree. C. to form volatile metal chlorides; removal of the fission product chlorides, transuranic product chlorides, and any nickel chloride and chromium chloride in a molten salt scrubber at approximately 400.degree. C.; fractional condensation of the remaining volatile chlorides at temperatures ranging from 164.degree. C. to 2.degree. C.; and regeneration and recovery of the transferred spent molten salt by vacuum distillation. The residual fission products, transuranic products, and nickel- and chromium chlorides are converted to fluorides or oxides for vitrification. The method offers the significant advantages of a single, compact process that is applicable to most of the diverse nuclear fuels, minimizes secondary wastes, segregates fissile uranium from the high level wastes to resolve potential criticality concerns, segregates nonradioactive wastes from the high level wastes for volume reduction, and produces a common waste form glass or glass-ceramic.

Christian, Jerry Dale (Idaho Falls, ID); Thomas, Thomas Russell (Rigby, ID); Kessinger, Glen F. (Idaho Falls, ID)

1998-01-01T23:59:59.000Z

99

Nickel-Metal-Hydride Batterie--High Energy Storage for Electric Vehicles  

NLE Websites -- All DOE Office Websites (Extended Search)

Freedomcar & Vehicle Technologies Program Freedomcar & Vehicle Technologies Program Nickel-Metal-Hydride Batteries - High Energy Storage for Electric Vehicles Background The key to making electric vehicles (EVs) practical is the development of batteries that can provide performance comparable with that of con ventional vehicles at a similar cost. Most EV batteries have limited energy storage capabili ties, permitting only relatively short driving distances before the batteries must be recharged. In 1991, under a coopera tive agreement with The U.S. Department of Energy (DOE), the United States Advanced Battery Consortium (USABC) initiated development of nickel- metal-hydride (NiMH) battery technology and established it as a prime mid-term candidate for use in EVs. DOE funding has been instru

100

Thermostat Metals  

Science Conference Proceedings (OSTI)

...A thermostat metal is a composite material (usually in the form of sheet or strip) that consists of two or more materials bonded together, of which one can be a nonmetal. Because the materials bonded together to form the composite differ in

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

METAL COMPOSITIONS  

DOE Patents (OSTI)

Alloys of uranium which are strong, hard, and machinable are presented, These alloys of uranium contain bctween 0.1 to 5.0% by weight of at least one noble metal such as rhodium, palladium, and gold. The alloys may be heat treated to obtain a product with iniproved tensile and compression strengths,

Seybolt, A.U.

1959-02-01T23:59:59.000Z

102

Energy Efficiency and Conservation Block Grant Program  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

1) Upgrade lighting and metal halide fixtures along Emma Street with light-emitting diode (LED) fixtures; 2) replace metal halide fixtures in Murphy and Hunt Parks; 3)...

103

Energy Conservation in Metals  

Science Conference Proceedings (OSTI)

About this Symposium. Meeting, 2010 TMS Annual Meeting & Exhibition. Symposium, Energy Conservation in Metals. Sponsorship, The Minerals, Metals and...

104

Advanced nickel-metal hydride cell development. Final report, September 1993--March 1996  

DOE Green Energy (OSTI)

Inert gas atomization using metal hydride alloys for a Ni/MH{sub x}cell was studied. Atomization of the alloys was demonstrated on a small production scale up to batch size of several kg. Relative performance of the atomized and nonatomized alloys was investigated for the electrode material in a Ni/MH{sub x} cell. The study included effects of charge-discharge rates, temperature, and particle size on cell voltage (polarization) and specific capacity. Results show that the specific capacity of the present atomized alloys was apprecialy smaller than that of the nonatomized powder, especially for initial cycles. Full activation of the atomized alloys oftentook several hundreds of cycles. However, no appreciable difference in discharge rate capability was observed with R10 and R12 alloys. Chemical compositions were indistinguishable, although the oxygen contents of the atomized alloys were always higher. Effects of Ni and Cu coating on alloy performance were studied after electroless coating; the coatings noticeably improved the electrode rate capability for all the alloys. The electrode polarization was esecially improved, but not the cycle life. Further studies are needed.

Lim, Hong S.

1996-03-01T23:59:59.000Z

105

Mechanochemical processing for metals and metal alloys  

DOE Patents (OSTI)

A set of processes for preparing metal powders, including metal alloy powders, by ambient temperature reduction of a reducible metal compound by a reactive metal or metal hydride through mechanochemical processing. The reduction process includes milling reactants to induce and complete the reduction reaction. The preferred reducing agents include magnesium and calcium hydride powders. A process of pre-milling magnesium as a reducing agent to increase the activity of the magnesium has been established as one part of the invention.

Froes, Francis H. (Moscow, ID); Eranezhuth, Baburaj G. (Moscow, ID); Prisbrey, Keith (Moscow, ID)

2001-01-01T23:59:59.000Z

106

Extracting metals directly from metal oxides  

DOE Patents (OSTI)

A method of extracting metals directly from metal oxides by exposing the oxide to a supercritical fluid solvent containing a chelating agent is described. Preferably, the metal is an actinide or a lanthanide. More preferably, the metal is uranium, thorium or plutonium. The chelating agent forms chelates that are soluble in the supercritical fluid, thereby allowing direct removal of the metal from the metal oxide. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is selected from the group consisting of .beta.-diketones, halogenated .beta.-diketones, phosphinic acids, halogenated phosphinic acids, carboxylic acids, halogenated carboxylic acids, and mixtures thereof. In especially preferred embodiments, at least one of the chelating agents is fluorinated. The method provides an environmentally benign process for removing metals from metal oxides without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the metal recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Smart, Neil G. (Moscow, ID); Phelps, Cindy (Moscow, ID)

1997-01-01T23:59:59.000Z

107

Extracting metals directly from metal oxides  

DOE Patents (OSTI)

A method of extracting metals directly from metal oxides by exposing the oxide to a supercritical fluid solvent containing a chelating agent is described. Preferably, the metal is an actinide or a lanthanide. More preferably, the metal is uranium, thorium or plutonium. The chelating agent forms chelates that are soluble in the supercritical fluid, thereby allowing direct removal of the metal from the metal oxide. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is selected from the group consisting of {beta}-diketones, halogenated {beta}-diketones, phosphinic acids, halogenated phosphinic acids, carboxylic acids, halogenated carboxylic acids, and mixtures thereof. In especially preferred embodiments, at least one of the chelating agents is fluorinated. The method provides an environmentally benign process for removing metals from metal oxides without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the metal recovered, to provide an economic, efficient process. 4 figs.

Wai, C.M.; Smart, N.G.; Phelps, C.

1997-02-25T23:59:59.000Z

108

PREPARATION OF PLUTONIUM HALIDES  

DOE Patents (OSTI)

A process ls presented for the preparation of plutonium trihalides. Plutonium oxide or a compound which may be readily converted to plutonlum oxide, for example, a plutonium hydroxide or plutonlum oxalate is contacted with a suitable halogenating agent. Speciflc agents mentioned are carbon tetrachloride, carbon tetrabromide, sulfur dioxide, and phosphorus pentachloride. The reaction is carried out under superatmospberic pressure at about 300 icient laborato C.

Davidson, N.R.; Katz, J.J.

1958-11-01T23:59:59.000Z

109

The formation of metallic nanoparticles in single crystal CaF{sub 2} under 157 nm excimer laser irradiation  

SciTech Connect

Single crystal calcium fluoride (CaF{sub 2}) is an important material for vacuum-ultraviolet optical components. Unfortunately, all metal halides tend to form defects when exposed to energetic particles and laser radiation, and these defects can degrade optical performance. Here we examine the consequences of exposing CaF{sub 2} to 157 nm excimer laser radiation and show that several tens of thousands of pulses at fluences near 1 J/cm{sup 2} can color the material. Absorption spectra of the exposed material confirm the formation of metallic calcium nanoparticles similar to those produced by other forms of energetic radiation. The rate of nanoparticle formation depends on the bulk temperature and displays a local maximum near 50 deg. C. Absorption measurements at 157 nm display a transient absorption component that grows during prolonged irradiation and disappears on time scales of several minutes after irradiation ceases. The implications of these effects in optical components are discussed.

Cramer, L.P.; Langford, S.C.; Dickinson, J.T. [Physics Department, Washington State University, Pullman, Washington 99164-2814 (United States)

2006-03-01T23:59:59.000Z

110

メタンハイドレート資源開発研究コンソーシアム 平成23年度事業報告 平成24年度事業計画 (概要) MH21プロジェクトリーダー 増田 昌敬  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

First Offshore MH Production Test First Offshore MH Production Test Takami Kawamoto JOGMEC June 7, 2013 1 機密性○ To conduct studies to establish the technological platform for commercialization of methane hydrate *Preparatory study for commercial production *Feasibility *Environmental Impacts *Overall evaluation of the total Program etc. Offshore Production Tests * 1 st Production Test - FY2012 * 2 nd Production Test - FY2014 Technological Studies * Designing and Manufacturing Systems for Flow Test * Studying Production Methods * Assessing Environmental Impacts * Resource Assessments Onshore Production Tests ・1 st Production Test 2002 ・ 2 nd Production Test in 2008 Resource Assessment in Eastern Nankai Trough ・Seismic

111

Fabrication of large-volume, low-cost ceramic lanthanum halide scintillators for gamma ray detection : final report for DHS/DNDO/TRDD project TA-01-SL01.  

SciTech Connect

This project uses advanced ceramic processes to fabricate large, optical-quality, polycrystalline lanthanum halide scintillators to replace small single crystals produced by the conventional Bridgman growth method. The new approach not only removes the size constraint imposed by the growth method, but also offers the potential advantages of both reducing manufacturing cost and increasing production rate. The project goal is to fabricate dense lanthanum halide ceramics with a preferred crystal orientation by applying texture engineering and solid-state conversion to reduce the thermal mechanical stress in the ceramic and minimize scintillation light scattering at grain boundaries. Ultimately, this method could deliver the sought-after high sensitivity and <3% energy resolution at 662 keV of lanthanum halide scintillators and unleash their full potential for advanced gamma ray detection, enabling rapid identification of radioactive materials in a variety of practical applications. This report documents processing details from powder synthesis, seed particle growth, to final densification and texture development of cerium doped lanthanum bromide (LaBr{sub 3}:Ce{sup +3}) ceramics. This investigation demonstrated that: (1) A rapid, flexible, cost efficient synthesis method of anhydrous lanthanum halides and their solid solutions was developed. Several batches of ultrafine LaBr{sub 3}:Ce{sup +3} powder, free of oxyhalide, were produced by a rigorously controlled process. (2) Micron size ({approx} 5 {micro}m), platelet shape LaBr{sub 3} seed particles of high purity can be synthesized by a vapor phase transport process. (3) High aspect-ratio seed particles can be effectively aligned in the shear direction in the ceramic matrix, using a rotational shear-forming process. (4) Small size, highly translucent LaBr{sub 3} (0.25-inch diameter, 0.08-inch thick) samples were successfully fabricated by the equal channel angular consolidation process. (5) Large size, high density, translucent LaBr{sub 3} ceramics samples (3-inch diameter, > 1/8-inch thick) were fabricated by hot pressing, demonstrating the superior manufacturability of the ceramic approach over single crystal growth methods in terms of size capability and cost. (6) Despite all these advances, evidence has shown that LaBr{sub 3} is thermally unstable at temperatures required for the densification process. This is particularly true for material near the surface where lattice defects and color centers can be created as bromine becomes volatile at high temperatures. Consequently, after densification these samples made using chemically prepared ultrafine powders turned black. An additional thermal treatment in a flowing bromine condition proved able to reduce the darkness of the surface layer for these densified samples. These observations demonstrated that although finer ceramic powders are desirable for densification due to a stronger driving force from their large surface areas, the same desirable factor can lead to lattice defects and color centers when these powders are densified at higher temperatures where material near the surface becomes thermally unstable.

Boyle, Timothy J.; Ottley, Leigh Anna M.; Yang, Pin; Chen, Ching-Fong; Sanchez, Margaret R.; Bell, Nelson Simmons

2008-10-01T23:59:59.000Z

112

Metallic Glass II  

Science Conference Proceedings (OSTI)

Aug 8, 2013 ... Application of Metallic Glass for High Performance Si Solar Cell: ... of the metallic glasses during heating is dependent on the thermal stability of...

113

Light Metals 2010  

Science Conference Proceedings (OSTI)

Feb 1, 2010 ... Softcover book: Light Metals 2008 Volume 2: Aluminum Reduction. Hardcover book and CD-ROM: Light Metals 2009...

114

Bulk Metallic Glasses IX  

Science Conference Proceedings (OSTI)

... of elements to form metallic-glass alloys] have resulted in the required cooling rate ... Bauschinger Effect in Metallic Glass Nanowires under Cyclic Loading.

115

Refractory Metals Committee  

Science Conference Proceedings (OSTI)

The Refractory Metals Committee is part of the Structural Materials Division. Our Mission: Includes all technical aspects of the science of refractory metals and...

116

Principal Metals Online  

Science Conference Proceedings (OSTI)

Topic Title: WEB RESOURCE: Principal Metals Online Topic Summary: Principal Metals inventory database. Created On: 2/9/2007 5:41 AM, Topic View:.

117

Bulk Metallic Glasses XI  

Science Conference Proceedings (OSTI)

Jul 15, 2013 ... A Bulk Metallic Glass with Record-breaking Damage Tolerance ... Oxidation on the Surface Characteristics of Zr-based Bulk Metallic Glasses.

118

21st Century Locomotive Technology: Quarterly Technical Status Report 21 DOE/AL68284-TSR21  

DOE Green Energy (OSTI)

Development of thermal analysis capabilities for a sodium metal halide battery system was initiated.

Lembit Salasoo

2008-04-29T23:59:59.000Z

119

Trending: Metal Oxo Bonds  

NLE Websites -- All DOE Office Websites (Extended Search)

Trending: Metal Oxo Bonds Trending: Metal Oxo Bonds Trending: Metal Oxo Bonds Print Wednesday, 29 May 2013 00:00 Metal oxides are important for scientific and technical applications in a variety of disciplines, including materials science, chemistry, and biology. Highly covalent metal-oxygen multiple bonds (metal oxos) are the building blocks of metal oxides and have a bearing on the oxide's desirable chemical, magnetic, electronic, and thermal properties. The lack of a more sophisticated grasp of bonding in metal oxides constitutes a roadblock to innovation in a wide variety of important emergent technologies, including industrial catalysis, biomimetic transformations, and artificial photosynthesis. To address this problem, a research team from four national laboratories, three Department of Energy synchrotron user facilities, and the University of Washington has applied spectroscopic and computational analyses to a number of metal oxides, quantifying trends in metal oxo bonding for groups of metals across the periodic table.

120

Method and making group IIB metal - telluride films and solar cells  

DOE Patents (OSTI)

A technique is disclosed forming thin films (13) of group IIB metal-telluride, such as Cd.sub.x Zn.sub.1-x Te (0.ltoreq.x.ltoreq.1), on a substrate (10) which comprises depositing Te (18) and at least one of the elements (19) of Cd, Zn, and Hg onto a substrate and then heating the elements to form the telluride. A technique is also provided for doping this material by chemically forming a thin layer of a dopant on the surface of the unreacted elements and then heating the elements along with the layer of dopant. A method is disclosed of fabricating a thin film photovoltaic cell which comprises depositing Te and at least one of the elements of Cd, Zn, and Hg onto a substrate which contains on its surface a semiconductor film (12) and then heating the elements in the presence of a halide of the Group IIB metals, causing the formation of solar cell grade Group IIB metal-telluride film and also causing the formation of a rectifying junction, in situ, between the semiconductor film on the substrate and the Group IIB metal-telluride layer which has been formed.

Basol, Bulent M. (Redondo Beach, CA); Kapur, Vijay K. (Northridge, CA)

1990-08-21T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

Corrosion of valve metals  

DOE Green Energy (OSTI)

A general survey related to the corrosion of valve metals or film-forming metals. The way these metals corrode with some general examples is described. Valve metals form relatively perfect oxide films with little breakdown or leakage when anodized. (FS)

Draley, J.E.

1976-01-01T23:59:59.000Z

122

Precious Metals Conversion Information  

Science Conference Proceedings (OSTI)

Precious Metals Conversion Information. The Office of Weights and Measures (OWM) has prepared a Conversion Factors ...

2012-11-21T23:59:59.000Z

123

METAL PRODUCTION AND CASTING  

DOE Patents (OSTI)

This patent covers a method and apparatus for collecting the molten metal produced by high temperature metal salt reduction. It consists essentially of subjecting the reaction vessel to centrifugal force in order to force the liberatcd molten metal into a coherent molten mass, and allowing it to solidify there. The apparatus is particularly suitable for use with small quantities of rare metals.

Magel, T.T.

1958-03-01T23:59:59.000Z

124

Ceramic to metal seal  

DOE Patents (OSTI)

Providing a high strength, hermetic ceramic to metal seal by essentially heating a wire-like metal gasket and a ceramic member, which have been chemically cleaned, while simultaneously deforming from about 50 to 95 percent the metal gasket against the ceramic member at a temperature of about 30 to 75 percent of the melting temperature of the metal gasket.

Snow, Gary S. (Albuquerque, NM); Wilcox, Paul D. (Albuquerque, NM)

1976-01-01T23:59:59.000Z

125

Trending: Metal Oxo Bonds  

NLE Websites -- All DOE Office Websites (Extended Search)

Trending: Metal Oxo Bonds Print Trending: Metal Oxo Bonds Print Metal oxides are important for scientific and technical applications in a variety of disciplines, including materials science, chemistry, and biology. Highly covalent metal-oxygen multiple bonds (metal oxos) are the building blocks of metal oxides and have a bearing on the oxide's desirable chemical, magnetic, electronic, and thermal properties. The lack of a more sophisticated grasp of bonding in metal oxides constitutes a roadblock to innovation in a wide variety of important emergent technologies, including industrial catalysis, biomimetic transformations, and artificial photosynthesis. To address this problem, a research team from four national laboratories, three Department of Energy synchrotron user facilities, and the University of Washington has applied spectroscopic and computational analyses to a number of metal oxides, quantifying trends in metal oxo bonding for groups of metals across the periodic table.

126

Trending: Metal Oxo Bonds  

NLE Websites -- All DOE Office Websites (Extended Search)

Trending: Metal Oxo Bonds Print Trending: Metal Oxo Bonds Print Metal oxides are important for scientific and technical applications in a variety of disciplines, including materials science, chemistry, and biology. Highly covalent metal-oxygen multiple bonds (metal oxos) are the building blocks of metal oxides and have a bearing on the oxide's desirable chemical, magnetic, electronic, and thermal properties. The lack of a more sophisticated grasp of bonding in metal oxides constitutes a roadblock to innovation in a wide variety of important emergent technologies, including industrial catalysis, biomimetic transformations, and artificial photosynthesis. To address this problem, a research team from four national laboratories, three Department of Energy synchrotron user facilities, and the University of Washington has applied spectroscopic and computational analyses to a number of metal oxides, quantifying trends in metal oxo bonding for groups of metals across the periodic table.

127

Trending: Metal Oxo Bonds  

NLE Websites -- All DOE Office Websites (Extended Search)

Trending: Metal Oxo Bonds Print Trending: Metal Oxo Bonds Print Metal oxides are important for scientific and technical applications in a variety of disciplines, including materials science, chemistry, and biology. Highly covalent metal-oxygen multiple bonds (metal oxos) are the building blocks of metal oxides and have a bearing on the oxide's desirable chemical, magnetic, electronic, and thermal properties. The lack of a more sophisticated grasp of bonding in metal oxides constitutes a roadblock to innovation in a wide variety of important emergent technologies, including industrial catalysis, biomimetic transformations, and artificial photosynthesis. To address this problem, a research team from four national laboratories, three Department of Energy synchrotron user facilities, and the University of Washington has applied spectroscopic and computational analyses to a number of metal oxides, quantifying trends in metal oxo bonding for groups of metals across the periodic table.

128

Trending: Metal Oxo Bonds  

NLE Websites -- All DOE Office Websites (Extended Search)

Trending: Metal Oxo Bonds Print Trending: Metal Oxo Bonds Print Metal oxides are important for scientific and technical applications in a variety of disciplines, including materials science, chemistry, and biology. Highly covalent metal-oxygen multiple bonds (metal oxos) are the building blocks of metal oxides and have a bearing on the oxide's desirable chemical, magnetic, electronic, and thermal properties. The lack of a more sophisticated grasp of bonding in metal oxides constitutes a roadblock to innovation in a wide variety of important emergent technologies, including industrial catalysis, biomimetic transformations, and artificial photosynthesis. To address this problem, a research team from four national laboratories, three Department of Energy synchrotron user facilities, and the University of Washington has applied spectroscopic and computational analyses to a number of metal oxides, quantifying trends in metal oxo bonding for groups of metals across the periodic table.

129

Data:564a3135-a0a4-42c8-93cf-ca55dbcbf90c | Open Energy Information  

Open Energy Info (EERE)

a0a4-42c8-93cf-ca55dbcbf90c a0a4-42c8-93cf-ca55dbcbf90c No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Algoma Utility Comm Effective date: 2008/05/28 End date if known: Rate name: Street Lighting Service - Option B - 100 W MH Sector: Lighting Description: Application: This schedule will be applied to municipal street lighting. Option B: Customer Owned and Utility Maintained. Power Cost Adjustment Clause: Charge per all kWh varies monthly. See schedule PCAC. Note: HPS = High Pressure Sodium MH = Metal Halide Source or reference: http://www.algomautilities.com/media/Electric_Rate_Tariff_Sheets.pdf

130

Data:Ac07146b-8d32-45e7-9042-85f065e602d6 | Open Energy Information  

Open Energy Info (EERE)

Ac07146b-8d32-45e7-9042-85f065e602d6 Ac07146b-8d32-45e7-9042-85f065e602d6 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Algoma Utility Comm Effective date: 2008/05/28 End date if known: Rate name: Street Lighting Service - Option A - 175 W MH Sector: Lighting Description: Application: This schedule will be applied to municipal street lighting. Option A: Utility Owned and Maintained. Power Cost Adjustment Clause: Charge per all kWh varies monthly. See schedule PCAC. Note: HPS = High Pressure Sodium MH = Metal Halide Source or reference: http://www.algomautilities.com/media/Electric_Rate_Tariff_Sheets.pdf

131

Data:Da8c4406-ba6e-4564-aa77-7003d74bee60 | Open Energy Information  

Open Energy Info (EERE)

06-ba6e-4564-aa77-7003d74bee60 06-ba6e-4564-aa77-7003d74bee60 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 1000W MH - Shoebox ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

132

Data:B86ebcf3-870c-4233-9e75-a0471a221774 | Open Energy Information  

Open Energy Info (EERE)

-870c-4233-9e75-a0471a221774 -870c-4233-9e75-a0471a221774 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 400W MH - Shoebox ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

133

Data:B37ad405-1bd7-40e7-9478-baf3c053a57e | Open Energy Information  

Open Energy Info (EERE)

05-1bd7-40e7-9478-baf3c053a57e 05-1bd7-40e7-9478-baf3c053a57e No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Algoma Utility Comm Effective date: 2008/05/28 End date if known: Rate name: Street Lighting Service - Option A - 100 W MH Sector: Lighting Description: Application: This schedule will be applied to municipal street lighting. Option A: Utility Owned and Maintained. Power Cost Adjustment Clause: Charge per all kWh varies monthly. See schedule PCAC. Note: HPS = High Pressure Sodium MH = Metal Halide Source or reference: http://www.algomautilities.com/media/Electric_Rate_Tariff_Sheets.pdf

134

Data:13c51b15-5cae-49e3-9ee6-400f38d52613 | Open Energy Information  

Open Energy Info (EERE)

-5cae-49e3-9ee6-400f38d52613 -5cae-49e3-9ee6-400f38d52613 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 175W MH - Torch ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

135

Data:71d6b6fd-5996-4692-8470-e8e9fd2cea39 | Open Energy Information  

Open Energy Info (EERE)

fd-5996-4692-8470-e8e9fd2cea39 fd-5996-4692-8470-e8e9fd2cea39 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 250W MH - Shoebox ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

136

Data:8528a9dd-9b7c-4f63-bc00-065e48d37e29 | Open Energy Information  

Open Energy Info (EERE)

dd-9b7c-4f63-bc00-065e48d37e29 dd-9b7c-4f63-bc00-065e48d37e29 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Algoma Utility Comm Effective date: 2008/05/28 End date if known: Rate name: Street Lighting Service - Option B - 175 W MH Sector: Lighting Description: Application: This schedule will be applied to municipal street lighting. Option B: Customer Owned and Utility Maintained. Power Cost Adjustment Clause: Charge per all kWh varies monthly. See schedule PCAC. Note: HPS = High Pressure Sodium MH = Metal Halide Source or reference: http://www.algomautilities.com/media/Electric_Rate_Tariff_Sheets.pdf

137

Metal-Air Batteries  

Science Conference Proceedings (OSTI)

Metal-air batteries have much higher specific energies than most currently available primary and rechargeable batteries. Recent advances in electrode materials and electrolytes, as well as new designs on metal-air batteries, have attracted intensive effort in recent years, especially in the development of lithium-air batteries. The general principle in metal-air batteries will be reviewed in this chapter. The materials, preparation methods, and performances of metal-air batteries will be discussed. Two main metal-air batteries, Zn-air and Li-air batteries will be discussed in detail. Other type of metal-air batteries will also be described.

Zhang, Jiguang; Bruce, Peter G.; Zhang, Gregory

2011-08-01T23:59:59.000Z

138

Alkali metal nitrate purification  

DOE Patents (OSTI)

A process is disclosed for removing contaminants from impure alkali metal nitrates containing them. The process comprises heating the impure alkali metal nitrates in solution form or molten form at a temperature and for a time sufficient to effect precipitation of solid impurities and separating the solid impurities from the resulting purified alkali metal nitrates. The resulting purified alkali metal nitrates in solution form may be heated to evaporate water therefrom to produce purified molten alkali metal nitrates suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of purified alkali metal nitrates.

Fiorucci, Louis C. (Hamden, CT); Morgan, Michael J. (Guilford, CT)

1986-02-04T23:59:59.000Z

139

Metal phthalocyanine catalysts  

DOE Patents (OSTI)

As a new composition of matter, alkali metal or ammonium or tetraalkylammonium diazidoperfluorophthalocyanatoferrate. Other embodiments of the invention comprise compositions wherein the metal of the coordination complex is cobalt, manganese and chromium.

Ellis, Jr., Paul E. (Downingtown, PA); Lyons, James E. (Wallingford, PA)

1994-01-01T23:59:59.000Z

140

Metal phthalocyanine catalysts  

DOE Patents (OSTI)

A new composition of matter is described which is an alkali metal or ammonium or tetraalkylammonium diazidoperfluorophthalocyanatoferrate. Other embodiments of the invention comprise compositions wherein the metal of the coordination complex is cobalt, manganese and chromium.

Ellis, P.E. Jr.; Lyons, J.E.

1994-10-11T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

Bulk Metallic Glasses X  

Science Conference Proceedings (OSTI)

Jul 31, 2012 ... Aerospace and Spacecraft Applications for Bulk Metallic Glasses and Matrix Composites Air Oxidation of a Binary Cu64.5Zr35.5 Bulk Metallic...

142

Bulk Metallic Glasses VII  

Science Conference Proceedings (OSTI)

Sponsorship, The Minerals, Metals and Materials Society ... Air-Oxidation of a ( Zr55Cu30Al10Ni5)98Er2 Bulk Metallic Glass at 350-500oc Anelastic...

143

Precision metal rulers  

Science Conference Proceedings (OSTI)

... precision metal rulers. Our customers include state bureaus of Weights and Measures and departments of Agriculture. We also ...

2011-10-28T23:59:59.000Z

144

Fasteners & Metals Program  

Science Conference Proceedings (OSTI)

Directory of Accredited Laboratories. Fasteners & Metals Program. The Fastener Quality Act (FQA), Public Law 101-592, was ...

2013-11-08T23:59:59.000Z

145

TMS Light Metals Publication  

Science Conference Proceedings (OSTI)

The following instructions should be used when submitting a manuscript for any TMS Light Metals proceedings volume. INTRODUCTION. Orientation to...

146

Refractory Metals 2011  

Science Conference Proceedings (OSTI)

Aug 2, 2010 ... TMS Structural Materials Division TMS: Refractory Metals Committee. Organizer( s), Omer Dogan, DOE National Energy Technology Laboratory

147

Durable metallized polymer mirror  

DOE Patents (OSTI)

A metallized polymer mirror construction is disclosed having improved durability against delamination and tunneling, comprising: an outer layer of polymeric material; a metal oxide layer underlying the outer layer of polymeric material; a silver reflective layer underneath the metal oxide layer; and a layer of adhesive attaching the silver layer to a substrate. 6 figs.

Schissel, P.O.; Kennedy, C.E.; Jorgensen, G.J.; Shinton, Y.D.; Goggin, R.M.

1994-11-01T23:59:59.000Z

148

PRODUCTION OF METALS  

DOE Patents (OSTI)

A process is described producing metallic thorium, titanium, zirconium, or hafnium from the fluoride. In the process, the fluoride is reduced with alkali or alkaline earth metal and a booster compound (e.g. iodine or a decomposable oxysalt) in a sealed bomb at superatmospheric pressure and a temperature above the melting point of the metal to be produced.

Spedding, F.H.; Wilhelm, H.A.; Keller, W.H.

1961-09-19T23:59:59.000Z

149

Progress in transition metal-based enantioselective catalysis  

E-Print Network (OSTI)

In Chapter 1, the first enantioselective cross-coupling reactions of racemic secondary benzylic halides are described (eq 1). This method was applied to the syntheses of intermediates employed by other groups in the ...

Arp, Forrest O

2008-01-01T23:59:59.000Z

150

Silica Embedded Metal Hydrides  

DOE Green Energy (OSTI)

A method to produce silica embedded metal hydride was developed. The product is a composite in which metal hydride particles are embedded in a matrix of silica. The silica matrix is highly porous. Hydrogen gas can easily reach the embedded metal hydride particles. The pores are small so that the metal hydride particles cannot leave the matrix. The porous matrix also protects the metal hydride particles from larger and reactive molecules such as oxygen, since the larger gas molecules cannot pass through the small pores easily. Tests show that granules of this composite can absorb hydrogen readily and withstand many cycles without making fines.

Heung, L.K. [Westinghouse Savannah River Company, AIKEN, SC (United States); Wicks, G.G.

1998-08-01T23:59:59.000Z

151

Extraction process for removing metallic impurities from alkalide metals  

DOE Patents (OSTI)

A development is described for removing metallic impurities from alkali metals by employing an extraction process wherein the metallic impurities are extracted from a molten alkali metal into molten lithium metal due to the immiscibility of the alkali metals in lithium and the miscibility of the metallic contaminants or impurities in the lithium. The purified alkali metal may be readily separated from the contaminant-containing lithium metal by simple decanting due to the differences in densities and melting temperatures of the alkali metals as compared to lithium.

Royer, Lamar T. (Knoxville, TN)

1988-01-01T23:59:59.000Z

152

Extraction process for removing metallic impurities from alkalide metals  

DOE Patents (OSTI)

A development is described for removing metallic impurities from alkali metals by employing an extraction process wherein the metallic impurities are extracted from a molten alkali metal into molten lithium metal due to the immiscibility of the alkali metals in lithium and the miscibility of the metallic contaminants or impurities in the lithium. The purified alkali metal may be readily separated from the contaminant-containing lithium metal by simple decanting due to the differences in densities and melting temperatures of the alkali metals as compared to lithium.

Royer, L.T.

1987-03-20T23:59:59.000Z

153

Sumitomo Metal Industries Ltd Sumitomo Metals | Open Energy Information  

Open Energy Info (EERE)

Sumitomo Metal Industries Ltd Sumitomo Metals Sumitomo Metal Industries Ltd Sumitomo Metals Jump to: navigation, search Name Sumitomo Metal Industries Ltd (Sumitomo Metals) Place Osaka-shi, Osaka, Japan Zip 540-0041 Sector Solar Product Engaged in the steel, engineering, and electronics businesses; works on fuel cell component technology and manufactures silicon wafers for the solar sector. References Sumitomo Metal Industries Ltd (Sumitomo Metals)[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Sumitomo Metal Industries Ltd (Sumitomo Metals) is a company located in Osaka-shi, Osaka, Japan . References ↑ "Sumitomo Metal Industries Ltd (Sumitomo Metals)" Retrieved from "http://en.openei.org/w/index.php?title=Sumitomo_Metal_Industries_Ltd_Sumitomo_Metals&oldid=351744"

154

FORMING PROTECTIVE FILMS ON METAL  

DOE Patents (OSTI)

Methods are described of inhibiting the corrosion of ferrous metal by contact with heavy liquid metals such as bismuth and gallium at temperatures above 500 icient laborato C generally by bringing nltrogen and either the metal zirconium, hafnium, or titanium into reactlve contact with the ferrous metal to form a thin adherent layer of the nitride of the metal and thereafter maintaining a fractional percentage of the metal absorbed in the heavy liquid metal in contact with the ferrous metal container. The general purpose for uslng such high boiling liquid metals in ferrous contalners would be as heat transfer agents in liquid-metal-fueled nuclear reactors.

Gurinsky, D.H.; Kammerer, O.F.; Sadofsky, J.; Weeks, J.R.

1958-12-16T23:59:59.000Z

155

Metal atomization spray nozzle  

DOE Patents (OSTI)

A spray nozzle for a magnetohydrodynamic atomization apparatus has a feed passage for molten metal and a pair of spray electrodes mounted in the feed passage. The electrodes, diverging surfaces which define a nozzle throat and diverge at an acute angle from the throat. Current passes through molten metal when fed through the throat which creates the Lorentz force necessary to provide atomization of the molten metal.

Huxford, Theodore J. (Harriman, TN)

1993-01-01T23:59:59.000Z

156

Supported metal alloy catalysts  

DOE Patents (OSTI)

A process of preparing a Group IV, V, or VI metal carbonitride including reacting a Group IV, V, or VI metal amide complex with ammonia to obtain an intermediate product; and, heating the intermediate product to temperatures and for times sufficient to form a Group IV, V, or VI metal carbonitride is provided together with the product of the process and a process of reforming an n-alkane by use of the product.

Barrera, Joseph (Albuquerque, NM); Smith, David C. (Santa Clara, CA)

2000-01-01T23:59:59.000Z

157

Metal atomization spray nozzle  

DOE Patents (OSTI)

A spray nozzle for a magnetohydrodynamic atomization apparatus has a feed passage for molten metal and a pair of spray electrodes mounted in the feed passage. The electrodes, diverging surfaces which define a nozzle throat and diverge at an acute angle from the throat. Current passes through molten metal when fed through the throat which creates the Lorentz force necessary to provide atomization of the molten metal. 6 figures.

Huxford, T.J.

1993-11-16T23:59:59.000Z

158

Metal atom oxidation laser  

DOE Patents (OSTI)

A chemical laser which operates by formation of metal or carbon atoms and reaction of such atoms with a gaseous oxidizer in an optical resonant cavity is described. The lasing species are diatomic or polyatomic in nature and are readily produced by exchange or other abstraction reactions between the metal or carbon atoms and the oxidizer. The lasing molecules may be metal or carbon monohalides or monoxides. (auth)

Jensen, R.J.; Rice, W.W.; Beattie, W.H.

1975-10-28T23:59:59.000Z

159

Metal atom oxidation laser  

DOE Patents (OSTI)

A chemical laser which operates by formation of metal or carbon atoms and reaction of such atoms with a gaseous oxidizer in an optical resonant cavity is described. The lasing species are diatomic or polyatomic in nature and are readily produced by exchange or other abstraction reactions between the metal or carbon atoms and the oxidizer. The lasing molecules may be metal or carbon monohalides or monoxides.

Jensen, R.J.; Rice, W.W.; Beattie, W.H.

1975-10-28T23:59:59.000Z

160

Characterization of Light Metals  

Science Conference Proceedings (OSTI)

Mar 15, 2012 ... Characterization of Grit Blasted Metallic Biomaterials by ... The grit blasting, a surface improvement treatment is used to enhance mechanical...

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

Metal Matrix Composites - TMS  

Science Conference Proceedings (OSTI)

METAL- MATRIX COMPOSITES UNDER MULTI- AXIAL LOADINGS: M. V. S. Ravisankar ... including the values of the stress exponent and the activation energy.

162

ELECTRON WELDING OF METALS  

SciTech Connect

The advantages and disadvantages of the electron welding of metals are briefly reviewed. Typical apparatuses used for electron welding are described. (J.S.R)

Stohr, J.-A.

1958-03-01T23:59:59.000Z

163

Strong Bond Activation with Late Transition-Metal Pincer Complexes as a Foundation for Potential Catalysis  

E-Print Network (OSTI)

Strong bond activation mediated by pincer ligated transiton-metal complexes has been the subject of intense study in recent years, due to its potential involvement in catalytic transformations. This dissertation has focused on the net heterolytic cleavage of B-H and B-B bonds across the N-Pd bond in a cationic (PNP)Pd fragment, the C-H oxidative addition to a (PNP)Ir center and the recent results on the C-H and C-O oxidative addition in reactions of aryl carboxylates with the (PNP)Rh fragment. Transition metal carbene and carbyne complexes are of great interest because of their role in a wide variety of catalytic reactions. Our work has resulted in the isolation of a rhodium(I) difluorocarbene. Reaction of the rhodium difluorocarbene complex with a silylium salt led to the C-F bond cleavage and the formation of a terminal fluorocarbyne complex. Reductive elimination is a critical step of cross coupling reactions. In order to examine the effect of the pincer ligand on the reductive elimination reactions from Rh(III), the first pi-accepting PNP ligand bearing pyrrolyl substituents was prepared and installed onto the rhodium center. Arylhalide (halide = Br, I) oxidative addition was achieved in the presence of donor ligands such as acetonitrile to form stable six-coordinate Rh(III) compounds. The C-O reductive elimination reactions in this system were also explored.

Zhu, Yanjun

2012-05-01T23:59:59.000Z

164

Final Report: Metal Perhydrides for Hydrogen Storage  

DOE Green Energy (OSTI)

Hydrogen is a promising energy source for the future economy due to its environmental friendliness. One of the important obstacles for the utilization of hydrogen as a fuel source for applications such as fuel cells is the storage of hydrogen. In the infrastructure of the expected hydrogen economy, hydrogen storage is one of the key enabling technologies. Although hydrogen possesses the highest gravimetric energy content (142 KJ/g) of all fuels, its volumetric energy density (8 MJ/L) is very low. It is desired to increase the volumetric energy density of hydrogen in a system to satisfy various applications. Research on hydrogen storage has been pursed for many years. Various storage technologies, including liquefaction, compression, metal hydride, chemical hydride, and adsorption, have been examined. Liquefaction and high pressure compression are not desired due to concerns related to complicated devices, high energy cost and safety. Metal hydrides and chemical hydrides have high gravimetric and volumetric energy densities but encounter issues because high temperature is required for the release of hydrogen, due to the strong bonding of hydrogen in the compounds. Reversibility of hydrogen loading and unloading is another concern. Adsorption of hydrogen on high surface area sorbents such as activated carbon and organic metal frameworks does not have the reversibility problem. But on the other hand, the weak force (primarily the van der Waals force) between hydrogen and the sorbent yields a very small amount of adsorption capacity at ambient temperature. Significant storage capacity can only be achieved at low temperatures such as 77K. The use of liquid nitrogen in a hydrogen storage system is not practical. Perhydrides are proposed as novel hydrogen storage materials that may overcome barriers slowing advances to a hydrogen fuel economy. In conventional hydrides, e.g. metal hydrides, the number of hydrogen atoms equals the total valence of the metal ions. One LiH molecule contains one hydrogen atom because the valence of a Li ion is +1. One MgH2 molecule contains two hydrogen atoms because the valence of a Mg ion is +2. In metal perhydrides, a molecule could contain more hydrogen atoms than expected based on the metal valance, i.e. LiH1+n and MgH2+n (n is equal to or greater than 1). When n is sufficiently high, there will be plenty of hydrogen storage capacity to meet future requirements. The existence of hydrogen clusters, Hn+ (n = 5, 7, 9, 11, 13, 15) and transition metal ion-hydrogen clusters, M+(H2)n (n = 1-6), such as Sc(H2)n+, Co(H2)n+, etc., have assisted the development of this concept. Clusters are not stable species. However, their existence stimulates our approach on using electric charges to enhance the hydrogen adsorption in a hydrogen storage system in this study. The experimental and modeling work to verify it are reported here. Experimental work included the generation of cold hydrogen plasma through a microwave approach, synthesis of sorbent materials, design and construction of lab devices, and the determination of hydrogen adsorption capacities on various sorbent materials under various electric field potentials and various temperatures. The results consistently show that electric potential enhances the adsorption of hydrogen on sorbents. NiO, MgO, activated carbon, MOF, and MOF and platinum coated activated carbon are some of the materials studied. Enhancements up to a few hundred percents have been found. In general, the enhancement increases with the electrical potential, the pressure applied, and the temperature lowered. Theoretical modeling of the hydrogen adsorption on the sorbents under the electric potential has been investigated with the density functional theory (DFT) approach. It was found that the interaction energy between hydrogen and sorbent is increased remarkably when an electric field is applied. This increase of binding energy offers a potential solution for DOE when looking for a compromise between chemisorption and physisorption for hydrogen storage. Bonding of chemisorption is too

Hwang, J-Y.; Shi, S.; Hackney, S.; Swenson, D.; Hu, Y.

2011-07-26T23:59:59.000Z

165

Porous metallic bodies  

DOE Patents (OSTI)

Porous metallic bodies having a substantially uniform pore size of less than about 200 microns and a density of less than about 25 percent theoretical, as well as the method for making them, are disclosed. Group IIA, IIIB, IVB, VB, and rare earth metal hydrides a

Landingham, R.L.

1984-03-13T23:59:59.000Z

166

Clean Metal Spray Forming  

Science Conference Proceedings (OSTI)

controlled transfer of liquid metal from the ESR pool to the spray forming system is performed using a ... heating to maintain superheat and avoid freezing of the liquid metal as it flows through the funnel. ... As is the case with all similar cross-.

167

Explosion metal welding  

SciTech Connect

Process parameters pertaining to welding similar and dissimilar metals using explosives are reviewed. The discussion centers on the interrelationship of physical parameters which play a part in achieving desirable metallurgical results. Present activities in explosion metal welding at LASL are presented and shown how they related to the interests of the ERDA community.

Popoff, A.A.

1976-01-01T23:59:59.000Z

168

Liquid metal hydrogen barriers  

DOE Patents (OSTI)

Hydrogen barriers which comprise liquid metals in which the solubility of hydrogen is low and which have good thermal conductivities at operating temperatures of interest. Such barriers are useful in nuclear fuel elements containing a metal hydride moderator which has a substantial hydrogen dissociation pressure at reactor operating temperatures.

Grover, George M. (Los Alamos, NM); Frank, Thurman G. (Los Alamos, NM); Keddy, Edward S. (Los Alamos, NM)

1976-01-01T23:59:59.000Z

169

PRODUCTION OF PLUTONIUM METAL  

DOE Patents (OSTI)

A process is given for producing plutonium metal by the reduction of plutonium chloride, dissolved in alkali metal chloride plus or minus aluminum chloride, with magnesium or a magnesium-aluminum alloy at between 700 and 800 deg C and separating the plutonium or plutonium-aluminum alloy formed from the salt.

Lyon, W.L.; Moore, R.H.

1961-01-17T23:59:59.000Z

170

Production of magnesium metal  

DOE Patents (OSTI)

A process of producing magnesium metal includes providing magnesium carbonate, and reacting the magnesium carbonate to produce a magnesium-containing compound and carbon dioxide. The magnesium-containing compound is reacted to produce magnesium metal. The carbon dioxide is used as a reactant in a second process. In another embodiment of the process, a magnesium silicate is reacted with a caustic material to produce magnesium hydroxide. The magnesium hydroxide is reacted with a source of carbon dioxide to produce magnesium carbonate. The magnesium carbonate is reacted to produce a magnesium-containing compound and carbon dioxide. The magnesium-containing compound is reacted to produce magnesium metal. The invention further relates to a process for production of magnesium metal or a magnesium compound where an external source of carbon dioxide is not used in any of the reactions of the process. The invention also relates to the magnesium metal produced by the processes described herein.

Blencoe, James G. (Harriman, TN); Anovitz, Lawrence M. (Knoxville, TN); Palmer, Donald A. (Oliver Springs, TN); Beard, James S. (Martinsville, VA)

2010-02-23T23:59:59.000Z

171

Business Center for Precious Metals  

NLE Websites -- All DOE Office Websites (Extended Search)

Department of Energy Business Center for Precious Metals Department of Energy Business Center for Precious Metals Becky Eddy National Nuclear Security Administration Y-12 Site...

172

Nonferrous Metals Society of China  

Science Conference Proceedings (OSTI)

The Nonferrous Metals Society of China (NFSoc) is a technological organization of scientists and technologists engaged in the nonferrous metals industry.

173

Metal RIE 1: Unaxis 790  

Science Conference Proceedings (OSTI)

... Scientific Opportunities / Applications: Physical milling of most metals; Anisotropic etching of metal films; Anisotropic etching of SiO 2 and SiN x. ...

2013-04-23T23:59:59.000Z

174

Actinide metal processing  

DOE Patents (OSTI)

A process for converting an actinide metal such as thorium, uranium, or plutonium to an actinide oxide material by admixing the actinide metal in an aqueous medium with a hypochlorite as an oxidizing agent for sufficient time to form the actinide oxide material and recovering the actinide oxide material is described together with a low temperature process for preparing an actinide oxide nitrate such as uranyl nitrate. Additionally, a composition of matter comprising the reaction product of uranium metal and sodium hypochlorite is provided, the reaction product being an essentially insoluble uranium oxide material suitable for disposal or long term storage.

Sauer, N.N.; Watkin, J.G.

1992-03-24T23:59:59.000Z

175

Actinide metal processing  

DOE Patents (OSTI)

This invention is comprised of a process of converting an actinide metal such as thorium, uranium, or plutonium to an actinide oxide material by admixing the actinide metal in an aqueous medium with a hypochlorite as an oxidizing agent for sufficient time to form the actinide oxide material and recovering the actinide oxide material is provided together with a low temperature process of preparing an actinide oxide nitrate such as uranyl nitrate. Additionally, a composition of matter comprising the reaction product of uranium metal and sodium hypochlorite is provided, the reaction product being an essentially insoluble uranium oxide material suitable for disposal or long term storage.

Sauer, N.N.; Watkin, J.G.

1991-04-05T23:59:59.000Z

176

Charged Metallic Clusters  

Science Conference Proceedings (OSTI)

Usually in Nuclear Physics the minimum of the liquid drop model (LDM) energy occurs at a mass asymmetry which is different from the minimum of shell correction. Charged metallic clusters are ideal emitters of singly ionized trimers because both LDM and shell correction are reaching a minimum for the same mass asymmetry corresponding to the emission of a charged particle with two delocalized electrons. Maximum dissociation energy (Q-value) is obtained for metallic clusters with high surface tension and low Wigner-Seitz radius (transition metals). The Q-values for spheroidal shapes are much larger than for hemispheroids.

Poenaru, D. N.; Gherghescu, R. A. [Horia Hulubei National Institute of Physics and Nuclear Engineering (IFIN-HH), Bucharest-Magurele (Romania); Frankfurt Institute for Advanced Studies, Johann Wolfgang Goethe University, Frankfurt am Main (Germany); Solov'yov, A. V.; Greiner, W. [Frankfurt Institute for Advanced Studies, Johann Wolfgang Goethe University, Frankfurt am Main (Germany)

2009-12-03T23:59:59.000Z

177

Liquid metal electric pump  

DOE Patents (OSTI)

An electrical pump for pumping liquid metals to high pressures in high temperature environments without the use of magnets or moving mechanical parts. The pump employs a non-porous solid electrolyte membrane, typically ceramic, specific to the liquid metal to be pumped. A DC voltage is applied across the thickness of the membrane causing ions to form and enter the membrane on the electrically positive surface, with the ions being neutralized on the opposite surface. This action provides pumping of the liquid metal from one side of the non-porous solid electrolyte membrane to the other. 3 figs.

Abbin, J.P.; Andraka, C.E.; Lukens, L.L.; Moreno, J.B.

1992-01-14T23:59:59.000Z

178

Divalent metal nanoparticles  

E-Print Network (OSTI)

Metal nanoparticles hold promise for many scientific and technological applications, such as chemical and biological sensors, vehicles for drug delivery, and subdiffraction limit waveguides. To fabricate such devices, a ...

DeVries, Gretchen Anne

2008-01-01T23:59:59.000Z

179

Production of magnesium metal  

DOE Patents (OSTI)

A process of producing magnesium metal includes providing magnesium carbonate, and reacting the magnesium carbonate to produce a magnesium-containing compound and carbon dioxide. The magnesium-containing compound is reacted to produce magnesium metal. The carbon dioxide is used as a reactant in a second process. In another embodiment of the process, a magnesium silicate is reacted with a caustic material to produce magnesium hydroxide. The magnesium hydroxide is reacted with a source of carbon dioxide to produce magnesium carbonate. The magnesium carbonate is reacted to produce a magnesium-containing compound and carbon dioxide. The magnesium-containing compound is reacted to produce magnesium metal. The invention also relates to the magnesium metal produced by the processes described herein.

Blencoe, James G. (Harriman, TN); Anovitz, Lawrence M. (Knoxville, TN); Palmer, Donald A. (Oliver Springs, TN); Beard, James S. (Martinsville, VA)

2012-04-10T23:59:59.000Z

180

Controlled Metal Photodeposition  

A reliable syntheses of semiconductor-metal heterostructure has been developed to enable application of materials in catalytic, magnetic, and opto-electronic devices, and Iowa State University, The Ames Laboratory's Contractor, is looking for ...

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

General Light Metals  

Science Conference Proceedings (OSTI)

Mar 3, 2011 ... A detailed literature survey indicates that vacuum sintering is able to produce ... In recent years, there is a high demand for light-weight metals foams. ... Each powder mixture's composition is determined by response surface...

182

Metal Matrix Composites II  

Science Conference Proceedings (OSTI)

Oct 29, 2013... of Al-AC8H/Al2O3p Metal Matrix Composites Produced by Stir Casting Route: Anne Zulfia1; Maman Ajiriyanto1; 1University of Indonesia

183

Molten metal reactors  

SciTech Connect

A molten metal reactor for converting a carbon material and steam into a gas comprising hydrogen, carbon monoxide, and carbon dioxide is disclosed. The reactor includes an interior crucible having a portion contained within an exterior crucible. The interior crucible includes an inlet and an outlet; the outlet leads to the exterior crucible and may comprise a diffuser. The exterior crucible may contain a molten alkaline metal compound. Contained between the exterior crucible and the interior crucible is at least one baffle.

Bingham, Dennis N; Klingler, Kerry M; Turner, Terry D; Wilding, Bruce M

2013-11-05T23:59:59.000Z

184

Lithium metal reduction of plutonium oxide to produce plutonium metal  

DOE Patents (OSTI)

A method is described for the chemical reduction of plutonium oxides to plutonium metal by the use of pure lithium metal. Lithium metal is used to reduce plutonium oxide to alpha plutonium metal (alpha-Pu). The lithium oxide by-product is reclaimed by sublimation and converted to the chloride salt, and after electrolysis, is removed as lithium metal. Zinc may be used as a solvent metal to improve thermodynamics of the reduction reaction at lower temperatures. Lithium metal reduction enables plutonium oxide reduction without the production of huge quantities of CaO--CaCl.sub.2 residues normally produced in conventional direct oxide reduction processes.

Coops, Melvin S. (Livermore, CA)

1992-01-01T23:59:59.000Z

185

PROCESS FOR PRODUCING URANIUM HALIDES  

DOE Patents (OSTI)

A process amd associated apparatus for producing UF/sub 4/ from U/sub 3/ O/sub 8/ by a fluidized'' technique are reported. The U/sub 3/O/sub 8/ is first reduced to UO/sub 2/ by reaction with hydrogen, and the lower oxide of uranium is then reacted with gaseous HF to produce UF/sub 4/. In each case the reactant gas is used, alone or in combination with inert gases, to fluidize'' the finely divided reactant solid. The complete setup of the plant equipment including bins, reactor and the associated piping and valving, is described. An auxiliary fluorination reactor allows for the direct production of UF/sub 6/ from UF/sub 4/ and fluorine gas, or if desired, UF/sub 4/ may be collected as the product.

Murphree, E.V.

1957-10-29T23:59:59.000Z

186

Liquid metal thermal electric converter  

DOE Patents (OSTI)

A liquid metal thermal electric converter which converts heat energy to electrical energy. The design of the liquid metal thermal electric converter incorporates a unique configuration which directs the metal fluid pressure to the outside of the tube which results in the structural loads in the tube to be compressive. A liquid metal thermal electric converter refluxing boiler with series connection of tubes and a multiple cell liquid metal thermal electric converter are also provided.

Abbin, Joseph P. (Albuquerque, NM); Andraka, Charles E. (Albuquerque, NM); Lukens, Laurance L. (Albuquerque, NM); Moreno, James B. (Albuquerque, NM)

1989-01-01T23:59:59.000Z

187

Method for forming metal contacts  

DOE Patents (OSTI)

Methods of forming metal contacts with metal inks in the manufacture of photovoltaic devices are disclosed. The metal inks are selectively deposited on semiconductor coatings by inkjet and aerosol apparatus. The composite is heated to selective temperatures where the metal inks burn through the coating to form an electrical contact with the semiconductor. Metal layers are then deposited on the electrical contacts by light induced or light assisted plating.

Reddington, Erik; Sutter, Thomas C; Bu, Lujia; Cannon, Alexandra; Habas, Susan E; Curtis, Calvin J; Miedaner, Alexander; Ginley, David S; Van Hest, Marinus Franciscus Antonius Maria

2013-09-17T23:59:59.000Z

188

Transition-Metal Hydrides  

NLE Websites -- All DOE Office Websites (Extended Search)

Transition-Metal Hydride Electrochromics Transition-Metal Hydride Electrochromics A new type of electrochromic hydride material has interesting and unusual properties. Thin Ni-Mg films, for example, are mirror-like in appearance and have very low visible transmittance. On exposure to hydrogen gas or on reduction in alkaline electrolyte, the films become transparent. The transition is believed to result from formation of nickel magnesium hydride, Mg2NiH4. Switchable mirrors based on rare earth hydrides were discovered in 1996 at Vrije University in the Netherlands, Rare earth-magnesium alloy films were subsequently found to be superior to the pure lanthanides in maximum transparency and mirror-state reflectivity by Philips Laboratories. The newer transition-metal types which use less expensive and less reactive materials were discovered at LBNL. This has now become a very active area of study with a network of researchers.

189

LEVELING METAL COATINGS  

DOE Patents (OSTI)

A method is described for applying metallic coatings to a cylinder of uranium. An aluminum-silicon coat is applied by a process consisting of first cleaning the article by immersion for 5 minutes in 50% nitric acid at 65 C. The article then is dipped through a flux, prepared by adding 10% sodium fluoride to 90% of a flux comprising 53% potassium chloride, 42% lithium chloride, and 5% sodium chloride at 560 for 2 minutes and then directly into a molten metal bath comprising 99% aluminun and 12% silicon at 620 C for 3 minutes. While the coating is yet molten the article is transferred to a pair of steel rollers and rolled until the coating solidifies. By varying the composition of the flux other metals such as zinc, lead or the like may be coated on uranium in a similar manner.

Gage, H.A.

1959-02-10T23:59:59.000Z

190

Are Batteries Ready for Plug-in Hybrid Buyers?  

E-Print Network (OSTI)

M. (2008) Emerging lithium-ion battery technologies forbattery chemistries: nickel-metal hydride (NiMH) and lithium-ion (battery chemistries, including nickel-metal hydride (NiMH) and several lithium-ion (

Axsen, Jonn; Kurani, Kenneth S; Burke, Andy

2009-01-01T23:59:59.000Z

191

Are batteries ready for plug-in hybrid buyers?  

E-Print Network (OSTI)

M. (2008) Emerging lithium-ion battery technologies forbattery chemistries: nickel-metal hydride (NiMH) and lithium-ion (battery chemistries, including nickel-metal hydride (NiMH) and several lithium-ion (

Axsen, Jonn; Kurani, Kenneth S.; Burke, Andrew

2008-01-01T23:59:59.000Z

192

Are Batteries Ready for Plug-in Hybrid Buyers?  

E-Print Network (OSTI)

M. , 2008. Emerging lithium-ion battery technologies forbattery chemistries: nickel- metal hydride (NiMH) and lithium-ion (battery chemistries, including nickel- metal hydride (NiMH) and several lithium-ion (

Axsen, Jonn; Burke, Andy; Kurani, Kenneth S

2010-01-01T23:59:59.000Z

193

Method for locating metallic nitride inclusions in metallic alloy ingots  

DOE Patents (OSTI)

A method of determining the location and history of metallic nitride and/or oxynitride inclusions in metallic melts. The method includes the steps of labeling metallic nitride and/or oxynitride inclusions by making a coreduced metallic-hafnium sponge from a mixture of hafnium chloride and the chloride of a metal, reducing the mixed chlorides with magnesium, nitriding the hafnium-labeled metallic-hafnium sponge, and seeding the sponge to be melted with hafnium-labeled nitride inclusions. The ingots are neutron activated and the hafnium is located by radiometric means. Hafnium possesses exactly the proper metallurgical and radiochemical properties for this use.

White, Jack C. (Albany, OR); Traut, Davis E. (Corvallis, OR); Oden, Laurance L. (Albany, OR); Schmitt, Roman A. (Corvallis, OR)

1992-01-01T23:59:59.000Z

194

Metallic carbon materials  

DOE Patents (OSTI)

Novel metallic forms of planar carbon are described, as well as methods of designing and making them. Nonhexagonal arrangements of carbon are introduced into a graphite carbon network essentially without destroying the planar structure. Specifically a form of carbon comprising primarily pentagons and heptagons, and having a large density of states at the Fermi level is described. Other arrangements of pentagons and heptagons that include some hexagons, and structures incorporating squares and octagons are additionally disclosed. Reducing the bond angle symmetry associated with a hexagonal arrangement of carbons increases the likelihood that the carbon material will have a metallic electron structure.

Cohen, Marvin Lou (Berkeley, CA); Crespi, Vincent Henry (Darien, IL); Louie, Steven Gwon Sheng (Berkeley, CA); Zettl, Alexander Karlwalter (Kensington, CA)

1999-01-01T23:59:59.000Z

195

Catalysis Without Precious Metals  

Science Conference Proceedings (OSTI)

Written for chemists in industry and academia, this ready reference and handbook summarizes recent progress in the development of new catalysts that do not require precious metals. The research thus presented points the way to how new catalysts may ultimately supplant the use of precious metals in some types of reactions, while highlighting the remaining challenges. This material is based upon work supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Office of Basic Energy Sciences.

Bullock, R. Morris

2010-11-01T23:59:59.000Z

196

Metal alloy identifier  

DOE Patents (OSTI)

To identify the composition of a metal alloy, sparks generated from the alloy are optically observed and spectrographically analyzed. The spectrographic data, in the form of a full-spectrum plot of intensity versus wavelength, provide the "signature" of the metal alloy. This signature can be compared with similar plots for alloys of known composition to establish the unknown composition by a positive match with a known alloy. An alternative method is to form intensity ratios for pairs of predetermined wavelengths within the observed spectrum and to then compare the values of such ratios with similar values for known alloy compositions, thereby to positively identify the unknown alloy composition.

Riley, William D. (Avondale, MD); Brown, Jr., Robert D. (Avondale, MD)

1987-01-01T23:59:59.000Z

197

Energy efficiency improvement and cost saving opportunities for the Corn Wet Milling Industry: An ENERGY STAR Guide for Energy and Plant Managers  

E-Print Network (OSTI)

efficiency motors Lighting Controls Replace metal halide HID with high-intensity Daylighting fluorescents Replace incandescent with fluorescent or CFL

Galitsky, Christina; Worrell, Ernst; Ruth, Michael

2003-01-01T23:59:59.000Z

198

Low Light Imaging for Power Outage and Fire Detection  

E-Print Network (OSTI)

.Metal halide 7.High pressure sodium 8.Low pressure sodium 9.Light emitting diode #12;Spectral Signatures

199

Physical and Electrochemical Properties of Ionic Liquids for Na ...  

Science Conference Proceedings (OSTI)

Development of Hybrid Supercapacitors for Portable Power Applications ... Planar Sodium Metal Halide Battery for Renewable Integration and Grid Applications.

200

Serpentine metal gasket  

DOE Patents (OSTI)

A metallic seal or gasket for use in the joining of cryogenic fluid conduits, the seal or gasket having a generally planar and serpentine periphery defining a central aperture. According to a preferred embodiment, the periphery has at least two opposing elongated serpentine sides and two opposing arcuate ends joining the opposing elongated serpentine sides and is of a hexagonal cross-section.

Rothgeb, Timothy Moore (Norfolk, VA); Reece, Charles Edwin (Yorktown, VA)

2009-06-02T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Metal halogen electrochemical cell  

DOE Patents (OSTI)

It has now been discovered that reduction in the coulombic efficiency of metal halogen cells can be minimized if the microporous separator employed in such cells is selected from one which is preferably wet by the aqueous electrolyte and is not wet substantially by the cathodic halogen.

Bellows, Richard J. (Hampton, NJ); Kantner, Edward (E. Brunswick, NJ)

1988-08-23T23:59:59.000Z

202

Weld Metal Metallurgical Handbook  

Science Conference Proceedings (OSTI)

This report is part of an ongoing series of metallurgical handbooks that are being developed for utility engineers to use in assessing metallurgical characteristics of any given alloy. This report focuses specifically on the weld metal metallurgical characteristics of carbon, low-alloy martensitic, and austenitic stainless steel welds.

2009-03-31T23:59:59.000Z

203

STRIPPING METAL COATINGS  

DOE Patents (OSTI)

A method is described for removing aluminumuranium-silicon alloy bonded to metallic U comprising subjecting the Al-U -Si alloy to treatment with hot concentrated HNO/sun 3/ to partially dissolve and embrittle the alloy and shot- blasting the embrittled alloy to loosen it from the U.

Siefen, H.T.; Campbell, J.M.

1959-02-01T23:59:59.000Z

204

Ductile transplutonium metal alloys  

DOE Patents (OSTI)

Alloys of Ce with transplutonium metals such as Am, Cm, Bk and Cf have properties making them highly suitable as souces of the transplutonium element, e.g., for use in radiation detector technology or as radiation sources. The alloys are ductile, homogeneous, easy to prepare and have a fairly high density.

Conner, W.V.

1981-10-09T23:59:59.000Z

205

Functional Metal Phosphonates  

E-Print Network (OSTI)

The primary goal of the work described in this dissertation was the incorporation of functionality into metal phosphonates. This was done in one of several ways. The first involved using phosphonate ligands that had covalently attached organic functional groups. In some cases, these ligands undergo reactions during the solvothermal syntheses which can impart new chemical reactivity. Another method used to introduce functionality was to partially or completely substitute metal atoms within phosphonate clusters to create materials which may have interesting magnetic properties. By controlling the way these clusters pack in the solids, their magnetic properties may be able to be augmented. The final method used to impart functionality to metal phosphonates was the incorporation of N-donor and bulky aryl groups into the phosphonate ligands. These influences caused structural variations which exposed potentially active sites within the materials, including both Lewis acidic and basic sites, as well as Bronsted acid sites. The first strategy was employed in the design of tetravalent metal phosphonates which have covalently incorporated bipyridine moieties. The materials are porous so that the bipyridine sites can chelate Pd atoms from solution, which can then be reduced to stable nanoparticles trapped within the phosphonate matrix. This approach was also used in the synthesis of surface-functionalized divalent metal phosphonates which exhibit interesting amine uptake properties. Solvent and cation substitution effects were used to control the packing and connectivity of phosphonate-based clusters. The selective substitution of metal atoms within the clusters may lead to interesting magnetic materials. In other work, N-donor and bulky phosphonates were used to influence the structure of several SnII phosphonates, which resulted in the discovery of a new layered structure type. The effect of the Sn-N interaction on the structures is investigated, and found to have significant effects on the structural units formed and how they pack in the solid state. The work presented herein represents only a small fraction of the rich chemistry of metal phosphonates. Creative researchers will continue to push boundaries and find new and interesting applications for phosphonate-based materials.

Perry, Houston Phillipp

2011-12-01T23:59:59.000Z

206

Recipients: The 2001 LMD Light Metals Award  

Science Conference Proceedings (OSTI)

The Minerals, Metals & Materials Society's Light Metals Division Light Metals Award, established in 1983, is awarded to the author(s) of a paper published in the...

207

Recipients: The 2003 LMD Light Metals Award  

Science Conference Proceedings (OSTI)

The Minerals, Metals & Materials Society's Light Metals Division Light Metals Award, established in 1983, is awarded to the author(s) of a paper published in the...

208

Recipients: The 2002 LMD Light Metals Award  

Science Conference Proceedings (OSTI)

The Minerals, Metals & Materials Society's Light Metals Division Light Metals Award, established in 1983, is awarded to the author(s) of a paper published in the...

209

Recipients: The 2004 LMD Light Metals Award  

Science Conference Proceedings (OSTI)

The Minerals, Metals & Materials Society's Light Metals Division Light Metals Award, established in 1983, is awarded to the author(s) of a paper published in the...

210

Metal-Ion-Mediated Reactions  

NLE Websites -- All DOE Office Websites (Extended Search)

Metal-Ion-Mediated Reactions Metal-Ion-Mediated Reactions Metal-Ion-Mediated Reactions Print Monday, 19 December 2011 18:29 While mononuclear, polynuclear, and polymeric metal complexes are most often synthesized by the reaction of a metal precursor and a presynthesized organic ligand, it is also possible to generate the ligand in situ from an easily available organic compound. This approach allows the reactivity of the metal ion to activate a proligand, transforming it through an in situ reaction, sometimes providing coordination compounds with ligands not accessible by conventional organic synthesis. The intense interest in the reactivity of coordinated ligands is mainly due to the necessity of interpreting the mechanisms of homogeneous metal-catalyzed processes, in which a substrate is activated upon its coordination to one or more metal sites. A coordinated oxime group contains three active sites (C, N, O) for reactivity.

211

Metal reduction kinetics in Shewanella  

Science Conference Proceedings (OSTI)

Motivation: Metal reduction kinetics have been studied in cultures of dissimilatory metal reducing bacteria which include the Shewanella oneidensis strain MR-1. Estimation of system parameters from time-series data faces obstructions in ...

Raman Lall; Julie Mitchell

2007-09-01T23:59:59.000Z

212

Purification of alkali metal nitrates  

DOE Patents (OSTI)

A process is disclosed for removing heavy metal contaminants from impure alkali metal nitrates containing them. The process comprises mixing the impure nitrates with sufficient water to form a concentrated aqueous solution of the impure nitrates, adjusting the pH of the resulting solution to within the range of between about 2 and about 7, adding sufficient reducing agent to react with heavy metal contaminants within said solution, adjusting the pH of the solution containing reducing agent to effect precipitation of heavy metal impurities and separating the solid impurities from the resulting purified aqueous solution of alkali metal nitrates. The resulting purified solution of alkali metal nitrates may be heated to evaporate water therefrom to produce purified molten alkali metal nitrate suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of alkali metal nitrates.

Fiorucci, Louis C. (Hamden, CT); Gregory, Kevin M. (Woodridge, IL)

1985-05-14T23:59:59.000Z

213

SURFACE TREATMENT OF METALLIC URANIUM  

DOE Patents (OSTI)

The treatment of metallic uranium to provide a surface to which adherent electroplates can be applied is described. Metallic uranium is subjected to an etchant treatment in aqueous concentrated hydrochloric acid, and the etched metal is then treated to dissolve the resulting black oxide and/or chloride film without destroying the etched metal surface. The oxide or chloride removal is effected by means of moderately concentrated nitric acid in 3 to 20 seconds.

Gray, A.G.; Schweikher, E.W.

1958-05-27T23:59:59.000Z

214

Electroless metal plating of plastics  

DOE Patents (OSTI)

Process for plating main group metals on aromatic polymers is carried out by the use of a nonaqueous solution of a salt of an alkali metal in a positive valence state and a main group metal in a negative valence state with contact between the solution and polymer providing a redox reaction causing the deposition of the main group metal and the reduction of the polymer. Products from the process exhibit useful decorative and electrical properties.

Krause, L.J.

1982-09-20T23:59:59.000Z

215

Inert electrode containing metal oxides, copper and noble metal  

DOE Patents (OSTI)

A cermet composite material is made by treating at an elevated temperature a mixture comprising a compound of iron and a compound of at least one other metal, together with an alloy or mixture of copper and a noble metal. The alloy or mixture preferably comprises particles having an interior portion containing more copper than noble metal and an exterior portion containing more noble metal than copper. The noble metal is preferably silver. The cermet composite material preferably includes alloy phase portions and a ceramic phase portion. At least part of the ceramic phase portion preferably has a spinel structure.

Ray, Siba P. (Murrysville, PA); Woods, Robert W. (New Kensington, PA); Dawless, Robert K. (Monroeville, PA); Hosler, Robert B. (Sarver, PA)

2000-01-01T23:59:59.000Z

216

Inert electrode containing metal oxides, copper and noble metal  

DOE Patents (OSTI)

A cermet composite material is made by treating at an elevated temperature a mixture comprising a compound of iron and a compound of at least one other metal, together with an alloy or mixture of copper and a noble metal. The alloy or mixture preferably comprises particles having an interior portion containing more copper than noble metal and an exterior portion containing more noble metal than copper. The noble metal is preferably silver. The cermet composite material preferably includes alloy phase portions and a ceramic phase portion. At least part of the ceramic phase portion preferably has a spinel structure.

Ray, Siba P. (Murrysville, PA); Woods, Robert W. (New Kensington, PA); Dawless, Robert K. (Monroeville, PA); Hosler, Robert B. (Sarver, PA)

2001-01-01T23:59:59.000Z

217

METHOD OF PURIFYING URANIUM METAL  

DOE Patents (OSTI)

The removal of lmpurities from uranlum metal can be done by a process conslstlng of contacting the metal with liquid mercury at 300 icient laborato C, separating the impunitycontalnlng slag formed, cooling the slag-free liquld substantlally below the point at which uranlum mercurlde sollds form, removlng the mercury from the solids, and recovering metallic uranium by heating the solids.

Blanco, R.E.; Morrison, B.H.

1958-12-23T23:59:59.000Z

218

Integrated decontamination process for metals  

DOE Patents (OSTI)

An integrated process for decontamination of metals, particularly metals that are used in the nuclear energy industry contaminated with radioactive material. The process combines the processes of electrorefining and melt refining to purify metals that can be decontaminated using either electrorefining or melt refining processes.

Snyder, Thomas S. (Oakmont, PA); Whitlow, Graham A. (Murrysville, PA)

1991-01-01T23:59:59.000Z

219

Fabrication of metallic glass structures  

DOE Patents (OSTI)

Amorphous metal powders or ribbons are fabricated into solid shapes of appreciable thickness by the application of compaction energy. The temperature regime wherein the amorphous metal deforms by viscous flow is measured. The metal powders or ribbons are compacted within the temperature regime.

Cline, C.F.

1983-10-20T23:59:59.000Z

220

PRODUCTION OF ACTINIDE METAL  

DOE Patents (OSTI)

A process of reducing actinide oxide to the metal with magnesium-zinc alloy in a flux of 5 mole% of magnesium fluoride and 95 mole% of magnesium chloride plus lithium, sodium, potassium, calcium, strontium, or barium chloride is presented. The flux contains at least 14 mole% of magnesium cation at 600-- 900 deg C in air. The formed magnesium-zinc-actinide alloy is separated from the magnesium-oxide-containing flux. (AEC)

Knighton, J.B.

1963-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

METAL COATING BATHS  

DOE Patents (OSTI)

A method is presented for restoring the effectiveness of bronze coating baths used for hot dip coating of uranium. Such baths, containing a high proportion of copper, lose their ability to wet uranium surfaces after a period of use. The ability of such a bath to wet uranium can be restored by adding a small amount of metallic aluminum to the bath, and skimming the resultant hard alloy from the surface.

Robinson, J.W.

1958-08-26T23:59:59.000Z

222

Ni-MH battery modelling for ambient intelligence applications  

E-Print Network (OSTI)

Mobile devices, like sensor networks and MEMS actuators use mobile power supplies to ensure energy for their operation. These are mostly batteries. The lifetime of the devices depends on the power consumption and on the quality and capacitance of the battery. Though the integrated circuits and their power consumption improve continually, their clock frequency also increases with the time, and the resultant power consumption seems not to vary, or slightly increase. On the other hand, the properties of batteries are developing much slower, necessitating the optimization of their usage on system level.

Szente-Varga, D; Rencz, M

2008-01-01T23:59:59.000Z

223

Study fo Ni-MH Battery Capacity Management.  

E-Print Network (OSTI)

??The topic of this study is to develop a battery capacity management system. The main purpose is to monitor the state of battery during charging (more)

Chang, Chiung-jen

2005-01-01T23:59:59.000Z

224

Spray casting of metallic preforms  

SciTech Connect

A metal alloy is melted in a crucible and ejected from the bottom of the crucible as a descending stream of molten metal. The descending stream is impacted with a plurality of primary inert gas jets surrounding the molten metal stream to produce a plume of atomized molten metal droplets. An inert gas is blown onto a lower portion of the plume with a plurality of auxiliary inert gas jets to deflect the plume into a more restricted pattern of high droplet density, thereby substantially eliminating unwanted overspray and resulting wasted material. The plume is projected onto a moving substrate to form a monolithic metallic product having generally parallel sides.

Flinn, John E. (Idaho Falls, ID); Burch, Joseph V. (Shelley, ID); Sears, James W. (Niskayuna, NY)

2000-01-01T23:59:59.000Z

225

Recycling Metals for the Environment - TMS  

Science Conference Proceedings (OSTI)

Jun 26, 2008 ... This article describes metal production from primary and secondary resources, recovering metals from waste streams and environmental...

226

Liquid Metal Processing and Casting 2013  

Science Conference Proceedings (OSTI)

Ceramic, Slag and Refractory Reactions with Liquid Metals - Refining, Evaporation and Gas/Metal Reactions - Fundamentals of Reactions involving Liquid...

227

Materials Sustainability: Digital Resource Center - Recycling Metals ...  

Science Conference Proceedings (OSTI)

Jul 2, 2008 ... This article describes metal production from primary and secondary resources, recovering metals from waste streams and environmental...

228

MESOPOROUS METAL OXIDE MICROSPHERE ELECTRODE COMPOSITIONS AND ...  

Compositions and methods of making are provided for mesoporous metal oxide microspheres electrodes. The mesoporous metal oxide microsphere ...

229

Hydrothermal alkali metal recovery process  

DOE Patents (OSTI)

In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by treating them with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of an added base to establish a pH during the treatment step that is higher than would otherwise be possible without the addition of the base. During the treating process the relatively high pH facilitates the conversion of water-insoluble alkali metal compounds in the alkali metal residues into water-soluble alkali metal constituents. The resultant aqueous solution containing water-soluble alkali metal constituents is then separated from the residue solids, which consist of the treated particles and any insoluble materials formed during the treatment step, and recycled to the gasification process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preferably, the base that is added during the treatment step is an alkali metal hydroxide obtained by water washing the residue solids produced during the treatment step.

Wolfs, Denise Y. (Houston, TX); Clavenna, Le Roy R. (Baytown, TX); Eakman, James M. (Houston, TX); Kalina, Theodore (Morris Plains, NJ)

1980-01-01T23:59:59.000Z

230

Hydrothermal alkali metal recovery process  

SciTech Connect

In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by treating them with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250/sup 0/F and about 700/sup 0/F and in the presence of an added base to establish a pH during the treatment step that is higher than would otherwise be possible without the addition of the base. During the treating process the relatively high pH facilitates the conversion of water-insoluble alkali metal compounds in the alkali metal residues into water-soluble alkali metal constituents. The resultant aqueous solution containing watersoluble alkali metal constituents is then separated from the residue solids, which consist of the treated particles and any insoluble materials formed during the treatment step, and recycled to the gasification process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preferably, the base that is added during the treatment step is an alkali metal hydroxide obtained by water washing the residue solids produced during the treatment step.

Clavenna, L.R.; Eakman, J.M.; Kalina, T.; Wolfs, D.Y.

1980-08-26T23:59:59.000Z

231

Dimensionally stable metallic hydride composition  

SciTech Connect

A stable, metallic hydride composition and a process for making such a composition. The composition comprises a uniformly blended mixture of a metal hydride, kieselguhr, and a ballast metal, all in the form of particles. The composition is made by subjecting a metal hydride to one or more hydrogen absorption/desorption cycles to disintegrate the hydride particles to less than approximately 100 microns in size. The particles are partly oxidized, then blended with the ballast metal and the kieselguhr to form a uniform mixture. The mixture is compressed into pellets and calcined. Preferably, the mixture includes approximately 10 vol. % or more kieselguhr and approximately 50 vol. % or more ballast. Metal hydrides that can be used in the composition include Zr, Ti, V, Nb, Pd, as well as binary, tertiary, and more complex alloys of La, Al, Cu, Ti, Co, Ni, Fe, Zr, Mg, Ca, Mn, and mixtures and other combinations thereof. Ballast metals include Al, Cu and Ni.

Heung, Leung K. (Aiken, SC)

1994-01-01T23:59:59.000Z

232

Dimensionally stable metallic hydride composition  

SciTech Connect

A stable, metallic hydride composition and a process for making such a composition are described. The composition comprises a uniformly blended mixture of a metal hydride, kieselguhr, and a ballast metal, all in the form of particles. The composition is made by subjecting a metal hydride to one or more hydrogen absorption/desorption cycles to disintegrate the hydride particles to less than approximately 100 microns in size. The particles are partly oxidized, then blended with the ballast metal and the kieselguhr to form a uniform mixture. The mixture is compressed into pellets and calcined. Preferably, the mixture includes approximately 10 vol. % or more kieselguhr and approximately 50 vol. % or more ballast. Metal hydrides that can be used in the composition include Zr, Ti, V, Nb, Pd, as well as binary, tertiary, and more complex alloys of La, Al, Cu, Ti, Co, Ni, Fe, Zr, Mg, Ca, Mn, and mixtures and other combinations thereof. Ballast metals include Al, Cu and Ni.

Heung, L.K.

1994-03-22T23:59:59.000Z

233

Reduction of Metal Oxide to Metal using Ionic Liquids  

Science Conference Proceedings (OSTI)

A novel pathway for the high efficiency production of metal from metal oxide means of electrolysis in ionic liquids at low temperature was investigated. The main emphasis was to eliminate the use of carbon and high temperature application in the reduction of metal oxides to metals. The emphasis of this research was to produce metals such as Zn, and Pb that are normally produced by the application of very high temperatures. The reduction of zinc oxide to zinc and lead oxide to lead were investigated. This study involved three steps in accomplishing the final goal of reduction of metal oxide to metal using ionic liquids: 1) Dissolution of metal oxide in an ionic liquid, 2) Determination of reduction potential using cyclic voltammetry (CV) and 3) Reduction of the dissolved metal oxide. Ionic liquids provide additional advantage by offering a wide potential range for the deposition. In each and every step of the process, more than one process variable has been examined. Experimental results for electrochemical extraction of Zn from ZnO and Pb from PbO using eutectic mixtures of Urea ((NH2)2CO) and Choline chloride (HOC2H4N(CH3)3+Cl-) or (ChCl) in a molar ratio 2:1, varying voltage and temperatures were carried out. Fourier Transform Infra-Red (FTIR) spectroscopy studies of ionic liquids with and without metal oxide additions were conducted. FTIR and induction coupled plasma spectroscopy (ICPS) was used in the characterization of the metal oxide dissolved ionic liquid. Electrochemical experiments were conducted using EG&G potentiostat/galvanostat with three electrode cell systems. Cyclic voltammetry was used in the determination of reduction potentials for the deposition of metals. Chronoamperometric experiments were carried out in the potential range of -0.6V to -1.9V for lead and -1.4V to -1.9V for zinc. The deposits were characterized using XRD and SEM-EDS for phase, morphological and elemental analysis. The results showed that pure metal was deposited on the cathode. Successful extraction of metal from metal oxide dissolved in Urea/ChCl (2:1) was accomplished. The current efficiencies were relatively high in both the metal deposition processes with current efficiency greater than 86% for lead and 95% for zinc. This technology will advance the metal oxide reduction process by increasing the process efficiency and also eliminate the production of CO2 which makes this an environmentally benign technology for metal extraction.

Dr. Ramana Reddy

2012-04-12T23:59:59.000Z

234

Corrosion protective coating for metallic materials  

DOE Patents (OSTI)

Corrosion protective coatings for metallic materials, particularly aluminum and aluminum alloys, produced with simple, low-cost equipment and materials other than toxic metals or metal salts, or metal cyanides. The metallic material is cleaned, degreased, and deoxidized, the surface is converted to a substantially alkaline condition, and the surface is chemically sealed with inorganic metal compounds.

Buchheit, Rudolph G. (Albuquerque, NM); Martinez, Michael A. (Albuquerque, NM)

1998-01-01T23:59:59.000Z

235

Metal nanoparticle inks  

DOE Patents (OSTI)

Stabilized silver particles comprise particles comprising silver, a short-chain capping agent adsorbed on the particles, and a long-chain capping agent adsorbed on the particles. The short-chain capping agent is a first anionic polyelectrolyte having a molecular weight (Mw) of at most 10,000, and the long-chain capping agent is a second anionic polyelectrolyte having a molecular weight (Mw) of at least 25,000. The stabilized silver particles have a solid loading of metallic silver of at least 50 wt %.

Lewis, Jennifer A. (Urbana, IL); Ahn, Bok Yeop (Champaign, IL); Duoss, Eric B. (Urbana, IL)

2011-04-12T23:59:59.000Z

236

COORDINATION CHEMISTRY OF METAL SURFACES AND METAL COMPLEXES  

E-Print Network (OSTI)

molecular coordination chemistry of CH3NC has been reported.features of this surface chemistry. ACKNOw"LEDGMENTS The1980 Catalysis~ COORDINATION CHEMISTRY OF METAL SURFACES AND

Muetterties, E.L.

2013-01-01T23:59:59.000Z

237

Impact Resistance of Carbon Fiber and Metallic Glass Fiber Metal ...  

Science Conference Proceedings (OSTI)

The combination of thin metallic sheets with carbon fiber composite results in a ... Ceramic Textile Composites under In Situ Loading at Ultrahigh Temperatures.

238

Metal to ceramic sealed joint  

DOE Patents (OSTI)

A metal to ceramic sealed joint which can withstand wide variations in temperature and maintain a good seal is provided for use in a device adapted to withstand thermal cycling from about 20 to about 1000 degrees C. The sealed joint includes a metal member, a ceramic member having an end portion, and an active metal braze forming a joint to seal the metal member to the ceramic member. The joint is positioned remote from the end portion of the ceramic member to avoid stresses at the ends or edges of the ceramic member. The sealed joint is particularly suited for use to form sealed metal to ceramic joints in a thermoelectric generator such as a sodium heat engine where a solid ceramic electrolyte is joined to metal parts in the system.

Lasecki, John V. (Livonia, MI); Novak, Robert F. (Farmington Hills, MI); McBride, James R. (Ypsilanti, MI)

1991-01-01T23:59:59.000Z

239

Metals removal from spent salts  

DOE Patents (OSTI)

A method and apparatus for removing metal contaminants from the spent salt of a molten salt oxidation (MSO) reactor is described. Spent salt is removed from the reactor and analyzed to determine the contaminants present and the carbonate concentration. The salt is dissolved in water, and one or more reagents may be added to precipitate the metal oxide and/or the metal as either metal oxide, metal hydroxide, or as a salt. The precipitated materials are filtered, dried and packaged for disposal as waste or can be immobilized as ceramic pellets. More than about 90% of the metals and mineral residues (ashes) present are removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be spray-dried and returned to the reactor for re-use. Salt solutions containing a carbonate concentration <20% require further clean-up using an ion exchange column, which yields salt solutions that contain less than 1.0 ppm of contaminants.

Hsu, Peter C. (Pleasanton, CA); Von Holtz, Erica H. (Livermore, CA); Hipple, David L. (Livermore, CA); Summers, Leslie J. (Livermore, CA); Brummond, William A. (Livermore, CA); Adamson, Martyn G. (Danville, CA)

2002-01-01T23:59:59.000Z

240

Metal to ceramic sealed joint  

DOE Patents (OSTI)

A metal to ceramic sealed joint which can withstand wide variations in temperature and maintain a good seal is provided for use in a device adapted to withstand thermal cycling from about 20 to about 1000 degrees C. The sealed joint includes a metal member, a ceramic member having an end portion, and an active metal braze forming a joint to seal the metal member to the ceramic member. The joint is positioned remote from the end portion of the ceramic member to avoid stresses at the ends or edges of the ceramic member. The sealed joint is particularly suited for use to form sealed metal to ceramic joints in a thermoelectric generator such as a sodium heat engine where a solid ceramic electrolyte is joined to metal parts in the system. 11 figures.

Lasecki, J.V.; Novak, R.F.; McBride, J.R.

1991-08-27T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

Metallic hydrogen research  

DOE Green Energy (OSTI)

Theoretical studies predict that molecular hydrogen can be converted to the metallic phase at very high density and pressure. These conditions were achieved by subjecting liquid hydrogen to isentropic compression in a magnetic-flux compression device. Hydrogen became electrically conducting at a density of about 1.06 g/cm/sup 3/ and a calculated pressure of about 2 Mbar. In the experimental device, a cylindrical liner, on implosion by high explosive, compresses a magnetic flux which in turn isentropically compresses a hydrogen sample; coaxial conical anvils prevent escape of the sample during compression. One anvil contains a coaxial cable that uses alumina ceramic as an insulator; this probe allows continuous measurement of the electrical conductivity of the hydrogen. A flash x-ray radiograph exposed during the experiment records the location of the sample-tube boundaries and permits calculation of the sample density. The theoretical underpinnings of the metallic transition of hydrogen are briefly summarized, and the experimental apparatus and technique, analytical methods, and results are described. 9 figures.

Burgess, T.J.; Hawke, R.S.

1978-11-16T23:59:59.000Z

242

Corrosion-resistant metal surfaces  

DOE Patents (OSTI)

The present invention relates to metal surfaces having thereon an ultrathin (e.g., less than ten nanometer thickness) corrosion-resistant film, thereby rendering the metal surfaces corrosion-resistant. The corrosion-resistant film includes an at least partially crosslinked amido-functionalized silanol component in combination with rare-earth metal oxide nanoparticles. The invention also relates to methods for producing such corrosion-resistant films.

Sugama, Toshifumi (Wading River, NY)

2009-03-24T23:59:59.000Z

243

Nonferrous Metal Melting -- Marketing Kit  

Science Conference Proceedings (OSTI)

The industrial sector increasingly relies on electric furnaces for nonferrous metal melting due to declining electricity cost, greater use of recycled secondary nonferrous materials, and tightened environmental regulations. This Nonferrous Metal Melting -- Marketing Kit is designed to help utility sales and marketing personnel perform a progressive analysis of electrotechnology applications in nonferrous metal melting systems. The kit is designed for utility personnel who have limited knowledge of the no...

2000-07-27T23:59:59.000Z

244

Metal-ceramic joint assembly  

DOE Patents (OSTI)

A metal-ceramic joint assembly in which a brazing alloy is situated between metallic and ceramic members. The metallic member is either an aluminum-containing stainless steel, a high chromium-content ferritic stainless steel or an iron nickel alloy with a corrosion protection coating. The brazing alloy, in turn, is either an Au-based or Ni-based alloy with a brazing temperature in the range of 9500 to 1200.degree. C.

Li, Jian (New Milford, CT)

2002-01-01T23:59:59.000Z

245

Metals Welded and Thickness Parameters  

Science Conference Proceedings (OSTI)

...more sheet metal stampings that do not require gas-tight or liquid-tight joints can be more economically joined by high-speed RSW than by

246

SOLDERING OF ALUMINUM BASE METALS  

DOE Patents (OSTI)

This patent deals with the soldering of aluminum to metals of different types, such as copper, brass, and iron. This is accomplished by heating the aluminum metal to be soldered to slightly above 30 deg C, rubbing a small amount of metallic gallium into the part of the surface to be soldered, whereby an aluminum--gallium alloy forms on the surface, and then heating the aluminum piece to the melting point of lead--tin soft solder, applying lead--tin soft solder to this alloyed surface, and combining the aluminum with the other metal to which it is to be soldered.

Erickson, G.F.

1958-02-25T23:59:59.000Z

247

Primary Metals - Compressor Motors Failing  

Science Conference Proceedings (OSTI)

This power quality (PQ) case study presents the investigation of four failures of compressor motors for a two stage chiller at a primary metals manufacturing facility.

2003-12-31T23:59:59.000Z

248

Method for preparing porous metal hydride compacts  

DOE Patents (OSTI)

A method for preparing porous metallic-matrix hydride compacts which can be repeatedly hydrided and dehydrided without disintegration. A mixture of a finely divided metal hydride and a finely divided matrix metal is contacted with a poison which prevents the metal hydride from dehydriding at room temperature and atmospheric pressure. The mixture of matrix metal and poisoned metal hydride is then compacted under pressure at room temperature to form porous metallic-matrix hydride compacts.

Ron, M.; Gruen, D.M.; Mendelsohn, M.H.; Sheft, I.

1980-01-21T23:59:59.000Z

249

Metal decontamination for waste minimization using liquid metal refining technology  

Science Conference Proceedings (OSTI)

The current Department of Energy Mixed Waste Treatment Project flowsheet indicates that no conventional technology, other than surface decontamination, exists for metal processing. Current Department of Energy guidelines require retrievable storage of all metallic wastes containing transuranic elements above a certain concentration. This project is in support of the National Mixed Low Level Waste Treatment Program. Because of the high cost of disposal, it is important to develop an effective decontamination and volume reduction method for low-level contaminated metals. It is important to be able to decontaminate complex shapes where surfaces are hidden or inaccessible to surface decontamination processes and destruction of organic contamination. These goals can be achieved by adapting commercial metal refining processes to handle radioactive and organic contaminated metal. The radioactive components are concentrated in the slag, which is subsequently vitrified; hazardous organics are destroyed by the intense heat of the bath. The metal, after having been melted and purified, could be recycled for use within the DOE complex. In this project, we evaluated current state-of-the-art technologies for metal refining, with special reference to the removal of radioactive contaminants and the destruction of hazardous organics. This evaluation was based on literature reports, industrial experience, plant visits, thermodynamic calculations, and engineering aspects of the various processes. The key issues addressed included radioactive partitioning between the metal and slag phases, minimization of secondary wastes, operability of the process subject to widely varying feed chemistry, and the ability to seal the candidate process to prevent the release of hazardous species.

Joyce, E.L. Jr.; Lally, B. [Los Alamos National Lab., NM (United States); Ozturk, B.; Fruehan, R.J. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Dept. of Materials Science and Engineering

1993-09-01T23:59:59.000Z

250

METAL EXTRACTION PROCESS  

DOE Patents (OSTI)

An improved method for extracting uranium from aqueous solutions by solvent extraction is presented. A difficulty encountered in solvent extraction operations using an organic extractant (e.g., tributyl phosphate dissolved in kerosene or carbon tetrachloride) is that emulsions sometimes form, and phase separation is difficult or impossible. This difficulty is overcome by dissolving the organic extractant in a molten wax which is a solid at operating temperatures. After cooling, the wax which now contains the extractant, is broken into small particles (preferably flakes) and this wax complex'' is used to contact the uranium bearing solutions and extract the metal therefrom. Microcrystalline petroleum wax and certain ethylene polymers have been found suitable for this purpose.

Lewis, G.W. Jr.; Rhodes, D.E.

1957-11-01T23:59:59.000Z

251

Physical Properties of Metals  

Science Conference Proceedings (OSTI)

Table 1   Some physical properties of metals at room temperature...0.176 ? ? ? Tantalum 16.6 0.1391 6.5 54.4 135.0 Technetium 11.5 ? 7.05 50.2 185.0 Tellurium 6.237 0.201 18.2 5.98??6.02 1??50 Terbium 8.230 0.1818 10.3 11.1 1150 Thallium 11.872 0.130 28 47 150 Thorium 11.8 0.11308 10.9 77 157 Thulium 9.321 0.1598 13.3 16.9 676 Tin 5.765 0.205 21 62.8 110 Titanium 4.507...

252

Creating bulk nanocrystalline metal.  

Science Conference Proceedings (OSTI)

Nanocrystalline and nanostructured materials offer unique microstructure-dependent properties that are superior to coarse-grained materials. These materials have been shown to have very high hardness, strength, and wear resistance. However, most current methods of producing nanostructured materials in weapons-relevant materials create powdered metal that must be consolidated into bulk form to be useful. Conventional consolidation methods are not appropriate due to the need to maintain the nanocrystalline structure. This research investigated new ways of creating nanocrystalline material, new methods of consolidating nanocrystalline material, and an analysis of these different methods of creation and consolidation to evaluate their applicability to mesoscale weapons applications where part features are often under 100 {micro}m wide and the material's microstructure must be very small to give homogeneous properties across the feature.

Fredenburg, D. Anthony (Georgia Institute of Technology, Atlanta, GA); Saldana, Christopher J. (Purdue University, West Lafayette, IN); Gill, David D.; Hall, Aaron Christopher; Roemer, Timothy John (Ktech Corporation, Albuquerque, NM); Vogler, Tracy John; Yang, Pin

2008-10-01T23:59:59.000Z

253

Liquid metal thermoacoustic engine  

DOE Green Energy (OSTI)

We are studying a liquid metal thermoacoustic engine both theoretically and experimentally. This type of engine promises to produce large quantities of electrical energy from heat at modest efficiency with no moving parts. A sound wave is usually thought of as consisting of pressure oscillations, but always attendant to the pressure oscillation are temperature oscillations. The combination produces a rich variety of ''thermoacoustic'' effects. These effects are usually so small that they are never noticed in everyday life; nevertheless under the right circumstances they can be harnessed to produce powerful heat engines, heat pumps, and refrigerators. In our liquid metal thermoacoustic engine, heat flow from a high temperature source to a low temperature sink generates a high-amplitude standing acoustic wave in liquid sodium. This acoustic power is converted to electric power by a simple magnetohydrodynamic effect at the acoustic oscillation frequency. We have developed a detailed thermoacoustic theory applicable to this engine, and find that a reasonably designed liquid sodium engine operating between 700/sup 0/C and 100/sup 0/C should generate about 60 W/cm/sup 2/ of acoustic power at about 1/3 of Carnot's efficiency. Construction of a 3000 W-thermal laboratory model engine has just been completed, and we have exciting preliminary experimental results as of the time of preparation of this manuscript showing, basically, that the engine works. We have also designed and built a 1 kHz liquid sodium magnetohydrodynamic generator and have extensive measurements on it. It is now very well characterized both experimentally and theoretically. The first generator of its kind, it already converts acoustic power to electric power with 40% efficiency. 16 refs., 5 figs.

Swift, G.W.; Migliori, A.; Wheatley, J.C.

1986-01-01T23:59:59.000Z

254

Appliances and Commercial Equipment Standards  

NLE Websites -- All DOE Office Websites (Extended Search)

High Intensity Discharge Lamps Test Procedures High Intensity Discharge Lamps Test Procedures Sign up for e-mail updates on regulations for this and other products High-intensity discharge (HID) lamps include mercury vapor (MV), metal halide (MH), and high-pressure sodium (HPS) lamps. The Department of Energy (DOE) is establishing test procedures for HID lamps. This rulemaking is mandated by the Energy Policy and Conservation Act (EPCA). ( 42 U.S.C. 6291-6309) This Rulemaking is related to the High-Intensity Discharge Lamps Standard and Test Procedure. Recent Updates | Public Meeting Information | Submitting Public Comments | Milestones and Documents | Related Rulemakings | Statutory Authority | Contact Information Recent Updates DOE published a notice of proposed rulemaking regarding test procedures for HID lamps. 76 FR 77914 (Dec. 15, 2011).

255

Data:D45500ec-a27b-481a-a5e3-9c927b664a5c | Open Energy Information  

Open Energy Info (EERE)

ec-a27b-481a-a5e3-9c927b664a5c ec-a27b-481a-a5e3-9c927b664a5c No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Algoma Utility Comm Effective date: 2008/05/28 End date if known: Rate name: Street Lighting Service - 250 W HPS(Overhead) Sector: Lighting Description: Application: This schedule will be applied to municipal street lighting. Power Cost Adjustment Clause: Charge per all kWh varies monthly. See schedule PCAC. Note: HPS = High Pressure Sodium MH = Metal Halide Source or reference: http://www.algomautilities.com/media/Electric_Rate_Tariff_Sheets.pdf Source Parent: Comments Applicability

256

Data:239dd8c3-2660-4fb5-a10f-200895eb226c | Open Energy Information  

Open Energy Info (EERE)

c3-2660-4fb5-a10f-200895eb226c c3-2660-4fb5-a10f-200895eb226c No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 250W HPS - Shoebox ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

257

Data:982a1454-aa93-4ab1-a5cd-76205b2d6aa6 | Open Energy Information  

Open Energy Info (EERE)

aa93-4ab1-a5cd-76205b2d6aa6 aa93-4ab1-a5cd-76205b2d6aa6 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 100W HPS - Traditional ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

258

Data:982fa5fd-b44a-4196-8c97-39a136f8ea38 | Open Energy Information  

Open Energy Info (EERE)

b44a-4196-8c97-39a136f8ea38 b44a-4196-8c97-39a136f8ea38 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 150W HPS - Expressway ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

259

Data:Fd4a1d85-7f5c-46aa-90b2-bccb09df9df3 | Open Energy Information  

Open Energy Info (EERE)

-7f5c-46aa-90b2-bccb09df9df3 -7f5c-46aa-90b2-bccb09df9df3 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Crisp County Power Comm Effective date: 2012/01/01 End date if known: Rate name: Rental Light Service-Parking Lot Shoebox- One Fixture (350/400 W MH/HPS) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide. Source or reference: ISU Documentation Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh):

260

Data:Ec8a2a34-0d66-487d-a4d3-3d24e442eb86 | Open Energy Information  

Open Energy Info (EERE)

4-0d66-487d-a4d3-3d24e442eb86 4-0d66-487d-a4d3-3d24e442eb86 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 250W HPS - Expressway ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

Data:D96a197b-661d-43e7-83c0-879ab36d94c2 | Open Energy Information  

Open Energy Info (EERE)

97b-661d-43e7-83c0-879ab36d94c2 97b-661d-43e7-83c0-879ab36d94c2 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 100W HPS - Cobrahead ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability

262

Data:Dfeb10f5-b315-4b62-880c-3b952e4d4e63 | Open Energy Information  

Open Energy Info (EERE)

Dfeb10f5-b315-4b62-880c-3b952e4d4e63 Dfeb10f5-b315-4b62-880c-3b952e4d4e63 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Algoma Utility Comm Effective date: 2008/05/28 End date if known: Rate name: Street Lighting Service - 200 W HPS(Overhead) Sector: Lighting Description: Application: This schedule will be applied to municipal street lighting. Power Cost Adjustment Clause: Charge per all kWh varies monthly. See schedule PCAC. Note: HPS = High Pressure Sodium MH = Metal Halide Source or reference: http://www.algomautilities.com/media/Electric_Rate_Tariff_Sheets.pdf Source Parent: Comments Applicability

263

Data:245bd7d1-d33d-4993-aba9-822ff9f1fdfc | Open Energy Information  

Open Energy Info (EERE)

-d33d-4993-aba9-822ff9f1fdfc -d33d-4993-aba9-822ff9f1fdfc No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 250W HPS - Cobrahead ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

264

Data:A4423bc0-5f8d-4ef2-a967-bea6ed1f5fc9 | Open Energy Information  

Open Energy Info (EERE)

A4423bc0-5f8d-4ef2-a967-bea6ed1f5fc9 A4423bc0-5f8d-4ef2-a967-bea6ed1f5fc9 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Nueces Electric Coop, Inc Effective date: 2009/11/20 End date if known: Rate name: Security/Street Light Service Metered 1000w Sector: Lighting Description: *Security/Street Light Service is available to Members, municipalities and governmental authorities in accordance with the Cooperative's Service Rules and Regulations for pole mounted area security and street lighting near the Cooperative's electric distribution lines with existing transformers. MV = Mercury Vapor; HPS = High Pressure Sodium; MH = Metal Halide; X= Cobra Head assembly.

265

Data:7d6e144f-1ee4-4317-9d4d-5000bbb042b0 | Open Energy Information  

Open Energy Info (EERE)

4f-1ee4-4317-9d4d-5000bbb042b0 4f-1ee4-4317-9d4d-5000bbb042b0 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Crisp County Power Comm Effective date: 2012/01/01 End date if known: Rate name: Rental Light Service-Parking Lot Shoebox- Two Fixture (350/400 W MH/HPS) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide. Source or reference: ISU Documentation Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh):

266

City of Bryant, South Dakota (Utility Company) | Open Energy Information  

Open Energy Info (EERE)

Bryant, South Dakota (Utility Company) Bryant, South Dakota (Utility Company) Jump to: navigation, search Name City of Bryant Place South Dakota Utility Id 2448 Utility Location Yes Ownership M NERC Location MRO Activity Transmission Yes References EIA Form EIA-861 Final Data File for 2010 - File1_a[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Utility Rate Schedules Grid-background.png Heavy Commercial Rate Commercial Light Commercial Rate Commercial Private Security Lights- (175 MV and 100W HPS) Lighting Private Security Lights- (400 Metal Halide) Lighting Private Security Lights- (400W MH) Lighting Residential Rate Residential Seasonal Electric Rate Commercial Average Rates Residential: $0.1050/kWh

267

Data:Ce257723-a06c-4647-a520-102fafcf2c22 | Open Energy Information  

Open Energy Info (EERE)

Ce257723-a06c-4647-a520-102fafcf2c22 Ce257723-a06c-4647-a520-102fafcf2c22 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Crisp County Power Comm Effective date: 2012/01/01 End date if known: Rate name: Rental Light Service-Post Top Fixtures- (Traditional MH 150/175W) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide. Source or reference: ISU Documentation Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh):

268

Data:532df7a5-5df5-475a-a247-86ac29f8f0d5 | Open Energy Information  

Open Energy Info (EERE)

a5-5df5-475a-a247-86ac29f8f0d5 a5-5df5-475a-a247-86ac29f8f0d5 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Algoma Utility Comm Effective date: 2008/05/28 End date if known: Rate name: Street Lighting Service - 100 W HPS(Overhead) Sector: Lighting Description: Application: This schedule will be applied to municipal street lighting. Power Cost Adjustment Clause: Charge per all kWh varies monthly. See schedule PCAC. Note: HPS = High Pressure Sodium MH = Metal Halide Source or reference: http://www.algomautilities.com/media/Electric_Rate_Tariff_Sheets.pdf Source Parent: Comments Applicability

269

Data:1ed95e55-77c3-4ba5-a97f-2ae396b39928 | Open Energy Information  

Open Energy Info (EERE)

5-77c3-4ba5-a97f-2ae396b39928 5-77c3-4ba5-a97f-2ae396b39928 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Crisp County Power Comm Effective date: 2012/01/01 End date if known: Rate name: Rental Light Service-Post Top Fixtures- (Torch MH 250W) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide. Source or reference: ISU Documentation Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months):

270

Data:Abebf4df-42b4-4191-a89f-831699aa0854 | Open Energy Information  

Open Energy Info (EERE)

Abebf4df-42b4-4191-a89f-831699aa0854 Abebf4df-42b4-4191-a89f-831699aa0854 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 150W HPS - Cobrahead ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability

271

Data:92d0a7d1-bb82-45db-994c-0dcc09e7cab4 | Open Energy Information  

Open Energy Info (EERE)

bb82-45db-994c-0dcc09e7cab4 bb82-45db-994c-0dcc09e7cab4 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 250W HPS - Traditional ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

272

Data:Dc676092-86ef-4bb7-80e3-b82a5cccd0d8 | Open Energy Information  

Open Energy Info (EERE)

2-86ef-4bb7-80e3-b82a5cccd0d8 2-86ef-4bb7-80e3-b82a5cccd0d8 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 400W HPS - Expressway ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability

273

Data:2ffcfa4e-d40e-4966-ad5f-08e2c6d81558 | Open Energy Information  

Open Energy Info (EERE)

ffcfa4e-d40e-4966-ad5f-08e2c6d81558 ffcfa4e-d40e-4966-ad5f-08e2c6d81558 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 400W HPS - Shoebox ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability

274

Data:68e73637-cd28-4a9c-9a21-63a07f0c4666 | Open Energy Information  

Open Energy Info (EERE)

7-cd28-4a9c-9a21-63a07f0c4666 7-cd28-4a9c-9a21-63a07f0c4666 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 150W HPS - Traditional ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability

275

Data:042eb420-7802-4b5a-9228-e829cba1421a | Open Energy Information  

Open Energy Info (EERE)

7802-4b5a-9228-e829cba1421a 7802-4b5a-9228-e829cba1421a No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Jefferson Electric Member Corp Effective date: 2010/11/01 End date if known: Rate name: STREET LIGHTING SERVICE ( 400W HPS - Cobrahead ) Sector: Lighting Description: Additional fees for poles and transformers may apply Source or reference: ISU Documentation Source Parent: Comments Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either high pressure sodium (HPS) or metal halide (MH), and poles conforming to Cooperative specifications. Applicability Demand (kW)

276

Appliances and Commercial Equipment Standards  

NLE Websites -- All DOE Office Websites (Extended Search)

High-Intensity Discharge Lamps Energy Conservation Standard High-Intensity Discharge Lamps Energy Conservation Standard Sign up for e-mail updates on regulations for this and other products High-intensity discharge (HID) lamps include mercury vapor (MV), metal halide (MH), and high-pressure sodium (HPS) lamps. The Department of Energy (DOE) is considering establishing energy conservation standards for certain HID lamps. This rulemaking is mandated by the Energy Policy and Conservation Act (EPCA). (42 USC 6311-6317) Recent Updates | Public Meeting Information | Submitting Public Comments | Milestones and Documents | Related Rulemakings | Statutory Authority | Contact Information Recent Updates DOE published a notice of public meeting and availability of interim technical support document regarding energy conservation standards for high-intensity discharge lamps. 78 FR 13566 (February 28, 2013).

277

Appliances and Commercial Equipment Standards  

NLE Websites -- All DOE Office Websites (Extended Search)

Metal Halide Lamp Fixtures Metal Halide Lamp Fixtures Sign up for e-mail updates on regulations for this and other products The Department of Energy (DOE) has regulated the energy efficiency level of metal halide lamp fixtures since 2007. A metal halide lamp fixture uses a metal halide lamp and a metal halide lamp ballast. The lamp is the light source and the ballast starts and regulates current. Metal halide fixtures or lighting systems provide lighting for parking lots and streets, flood lighting, athletics facilities, big-box stores, and warehouses. The current standards will save approximately 6.4 quads of energy and result in approximately $9.6 billion in energy bill savings for products shipped from 2009-2038. The standard will avoid about 93.6 million metric tons of carbon dioxide emissions.

278

Nanostructured metal-polyaniline composites  

DOE Patents (OSTI)

Metal-polyaniline (PANI) composites are provided together with a process of preparing such composites by an electrodeless process. The metal of the composite can have nanoscale structural features and the composites can be used in applications such as catalysis for hydrogenation reactions and for analytical detection methods employing SERS.

Wang, Hsing-Lin (Los Alamos, NM); Li, Wenguang (Elgin, IL); Bailey, James A. (Los Alamos, NM); Gao, Yuan (Brewer, ME)

2010-08-31T23:59:59.000Z

279

Metal recovery from porous materials  

DOE Patents (OSTI)

The present invention relates to recovery of metals. More specifically, the present invention relates to the recovery of plutonium and other metals from porous materials using microwaves. The United States Government has rights in this invention pursuant to Contract No. DE-AC09-89SR18035 between the US Department of Energy and Westinghouse Savannah River Company.

Sturcken, E.F.

1991-01-01T23:59:59.000Z

280

Semantic search | Open Energy Information  

Open Energy Info (EERE)

100 | 250 | 500) 175W Mercury Vapor Contemporary Style Decorative Post Top Luminaires Lighting 175W Metal Halide Acorn Style Decorative Post Top Luminaires Lighting 175W Metal...

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Recipient: 1997 LMD Light Metals Technical Service Award  

Science Conference Proceedings (OSTI)

TMS Logo. Recipient: 1997 LMD Light Metals Technical Service Award. The Minerals, Metals & Materials Society's Light Metals Division Light Metals Technical...

282

Casimir Repulsion between Metallic Objects in Vacuum  

E-Print Network (OSTI)

We give an example of a geometry in which two metallic objects in vacuum experience a repulsive Casimir force. The geometry consists of an elongated metal particle centered above a metal plate with a hole. We prove that ...

Levin, Michael

283

Method for controlled hydrogen charging of metals  

DOE Patents (OSTI)

A method for controlling hydrogen charging of hydride forming metals through a window of a superimposed layer of a non-hydriding metal overlying the portion of the hydride forming metals to be charged.

Cheng, Bo-Ching (Fremont, CA); Adamson, Ronald B. (Fremont, CA)

1984-05-29T23:59:59.000Z

284

METHOD OF MAKING ALLOYS OF BERYLLIUM WITH PLUTONIUM AND THE LIKE  

DOE Patents (OSTI)

The production or alloys of beryllium with one or more of the metals uranium, plutonium, actinium, americium, curium, thorium, and cerium is described. A halide salt or the metal to be alloyed with the beryllium is heated at l3O0 deg C in the presence of beryllium to reduce the halide to metal and cause the latter to alloy directly with the beryllium. Although the heavy metal halides are more stable, thermodynamically, than the beryllium halides, the reducing reaction proceeds to completion if the beryllium halide product is continuously removed by vacuum distillation.

Runnals, O.J.C.

1959-02-24T23:59:59.000Z

285

METHOD OF MAKING ALLOYS OF BERYLLIUM WITH PLUTONIUM AND THE LIKE  

DOE Patents (OSTI)

The production of alloys of beryllium with one or more of the metals uranium, plutonium, actinium, americium, curium, thorium, and cerium are described. A halide salt of the metal to be alloyed with the beryllium is heated at 1300 deg C in the presence of beryllium to reduce the halide to metal and cause the latter to alloy directly with the beryllium. Although the heavy metal halides are more stable, thermodynamically, than the beryllium halides, the reducing reaction proceeds to completion if the beryllium halide product is continuously removed by vacuum distillation.

Runnals, O.J.C.

1959-02-24T23:59:59.000Z

286

Catalysis using hydrous metal oxide ion exchangers  

DOE Patents (OSTI)

In a process which is catalyzed by a catalyst comprising an active metal on a carrier, said metal being active as a catalyst for the process, an improvement is provided wherein the catalyst is a hydrous, alkali metal or alkaline earth metal titanate, zirconate, niobate or tantalate wherein alkali or alkaline earth metal cations have been exchanged with a catalytically effective amount of cations of said metal.

Dosch, R.G.; Stephens, H.P.; Stohl, F.V.

1983-07-21T23:59:59.000Z

287

Catalysis using hydrous metal oxide ion exchanges  

DOE Patents (OSTI)

In a process which is catalyzed by a catalyst comprising an active metal on a carrier, said metal being active as a catalyst for the process, an improvement is provided wherein the catalyst is a hydrous, alkali metal or alkaline earth metal titanate, zirconate, niobate or tantalate wherein alkali or alkaline earth metal cations have been exchanged with a catalytically effective amount of cations of said metal.

Dosch, Robert G. (Albuquerque, NM); Stephens, Howard P. (Albuquerque, NM); Stohl, Frances V. (Albuquerque, NM)

1985-01-01T23:59:59.000Z

288

Method of coating metal surfaces to form protective metal coating thereon  

DOE Patents (OSTI)

A process is disclosed for forming a protective metal coating on a metal surface using a flux consisting of an alkali metal fluoride, an alkaline earth metal fluoride, an alkali metal fluoaluminate, an alkali metal fluosilicate, and mixtures thereof. The flux, in particulate form, is mixed with particles of a metal coating material which may comprise aluminum, chromium, mixtures thereof, and alloys containing at least 50 wt. % aluminum and the particulate mixture is applied to the metal surface in a single step, followed by heating the coated metal surface to a temperature sufficient to cause the metal coating material to react with the metal surface to form a protective reaction product in the form of a metal coating bonded to the metal surface. The metal surface which reacts with the metal coating material to form the protective coating may comprise Fe, Co, Ni, Ti, V, Cr, Mn, Zr, Nb, Mo, Tc, Hf, Ta, W, Re and alloys thereof.

Krikorian, Oscar H. (Danville, CA); Curtis, Paul G. (Tracy, CA)

1992-01-01T23:59:59.000Z

289

Method of coating metal surfaces to form protective metal coating thereon  

DOE Patents (OSTI)

A process is disclosed for forming a protective metal coating on a metal surface using a flux consisting of an alkali metal fluoride, an alkaline earth metal fluoride, an alkali metal fluoaluminate, an alkali metal fluosilicate, and mixtures thereof. The flux, in particulate form, is mixed with particles of a metal coating material which may comprise aluminum, chromium, mixtures thereof, and alloys containing at least 50 wt. % aluminum and the particulate mixture is applied to the metal surface in a single step, followed by heating the coated metal surface to a temperature sufficient to cause the metal coating material to react with the metal surface to form a protective reaction product in the form of a metal coating bonded to the metal surface. The metal surface which reacts with the metal coating material to form the protective coating may comprise Fe, Co, Ni, Ti, V, Cr, Mn, Zr, Nb, Mo, Tc, Hf, Ta, W, Re and alloys thereof. 1 figure.

Krikorian, O.H.; Curtis, P.G.

1992-03-31T23:59:59.000Z

290

Quinary metallic glass alloys  

DOE Patents (OSTI)

At least quinary alloys form metallic glass upon cooling below the glass transition temperature at a rate less than 10.sup.3 K/s. Such alloys comprise zirconium and/or hafnium in the range of 45 to 65 atomic percent, titanium and/or niobium in the range of 4 to 7.5 atomic percent, and aluminum and/or zinc in the range of 5 to 15 atomic percent. The balance of the alloy compositions comprise copper, iron, and cobalt and/or nickel. The composition is constrained such that the atomic percentage of iron is less than 10 percent. Further, the ratio of copper to nickel and/or cobalt is in the range of from 1:2 to 2:1. The alloy composition formula is: (Zr,Hf).sub.a (Al,Zn).sub.b (Ti,Nb).sub.c (Cu.sub.x Fe.sub.y (Ni,Co).sub.z).sub.d wherein the constraints upon the formula are: a ranges from 45 to 65 atomic percent, b ranges from 5 to 15 atomic percent, c ranges from 4 to 7.5 atomic percent, d comprises the balance, d.multidot.y is less than 10 atomic percent, and x/z ranges from 0.5 to 2.

Lin, Xianghong (Pasadena, CA); Johnson, William L. (Pasadena, CA)

1998-01-01T23:59:59.000Z

291

Quinary metallic glass alloys  

DOE Patents (OSTI)

At least quinary alloys form metallic glass upon cooling below the glass transition temperature at a rate less than 10{sup 3}K/s. Such alloys comprise zirconium and/or hafnium in the range of 45 to 65 atomic percent, titanium and/or niobium in the range of 4 to 7.5 atomic percent, and aluminum and/or zinc in the range of 5 to 15 atomic percent. The balance of the alloy compositions comprise copper, iron, and cobalt and/or nickel. The composition is constrained such that the atomic percentage of iron is less than 10 percent. Further, the ratio of copper to nickel and/or cobalt is in the range of from 1:2 to 2:1. The alloy composition formula is: (Zr,Hf){sub a}(Al,Zn){sub b}(Ti,Nb){sub c}(Cu{sub x}Fe{sub y}(Ni,Co){sub z}){sub d} wherein the constraints upon the formula are: a ranges from 45 to 65 atomic percent, b ranges from 5 to 15 atomic percent, c ranges from 4 to 7.5 atomic percent, d comprises the balance, d{hor_ellipsis}y is less than 10 atomic percent, and x/z ranges from 0.5 to 2.

Lin, X.; Johnson, W.L.

1998-04-07T23:59:59.000Z

292

Engineering Metal Impurities in Multicrystalline Silicon Solar...  

NLE Websites -- All DOE Office Websites (Extended Search)

Engineering Metal Impurities in Multicrystalline Silicon Solar Cells Print Transition metals are one of the main culprits in degrading the efficiency of multicrystalline solar...

293

Industrial Ecology and Metal Production - TMS  

Science Conference Proceedings (OSTI)

Jul 2, 2008 ... Topic Title: Powerpoint: Industrial Ecology and Metal Production Topic Summary: Metal extraction is on the the most Earth-intrusive industrial...

294

BEHAVIOR OF METALLIC INCLUSIONS IN URANIUM DIOXIDE  

E-Print Network (OSTI)

Metallic Inclusions in Uranium Dioxide", LBL-11117 (1980).in Hypostoichiornetric Uranium Dioxide 11 , LBL-11095 (OF METALLIC INCLUSIONS IN URANIUM DIOXIDE Rosa L. Yang and

Yang, Rosa L.

2013-01-01T23:59:59.000Z

295

Metals Thin-Films Information at NIST  

Science Conference Proceedings (OSTI)

NIST Home > Metals Thin-Films Information at NIST. Metals Thin-Films Information at NIST. (the links below are a compilation ...

2010-05-24T23:59:59.000Z

296

Recycling Metals Using the MOCVD Process  

Science Conference Proceedings (OSTI)

Aug 1, 2000 ... Secondly, the volatile metal organic compound is purified by fractional distillation. Thirdly, the purified metal organic compound is decomposed...

297

Bulk Metallic Glasses VIII - Programmaster.org  

Science Conference Proceedings (OSTI)

Aug 2, 2010 ... Sponsorship, The Minerals, Metals and Materials Society .... The Oxidation Behavior of an FeCo-Based Bulk Metallic Glass at 600 - 700C.

298

Molten Metal Safety Approach through a Network  

Science Conference Proceedings (OSTI)

Abstract Scope, Molten Metal explosion or splash is a major risk encountered in the ... In-Line Salt-ACD: A ChlorineFree Technology for Metal Treatment.

299

About Rare Earth Metals | Ames Laboratory  

NLE Websites -- All DOE Office Websites (Extended Search)

About Rare Earth Metals About Rare Earth Metals What Are Rare Earths? Ames Laboratory's Materials Preparation Center The Ames Process for Purification of Rare...

300

Metal and Polymer Matrix Composites  

Science Conference Proceedings (OSTI)

Aluminum-fly Ash Composites Produced by Powder Metallurgy Processing Characterisation of Al-AC8H/Al2O3p Metal Matrix Composites Produced by Stir...

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

Nanostructured Metal Oxide Anodes (Presentation)  

DOE Green Energy (OSTI)

This summarizes NREL's FY09 battery materials research activity in developing metal oxide nanostructured anodes to enable high-energy, durable and affordable li-ion batteries for HEVs and PHEVs.

Dillon, A. C.; Riley, L. A.; Lee, S.-H.; Kim, Y.-H.; Ban, C.; Gillaspie, D. T.; Pesaran, A.

2009-05-01T23:59:59.000Z

302

Nanostructured Metal Oxide Anodes (Presentation)  

SciTech Connect

This summarizes NREL's FY09 battery materials research activity in developing metal oxide nanostructured anodes to enable high-energy, durable and affordable li-ion batteries for HEVs and PHEVs.

Dillon, A. C.; Riley, L. A.; Lee, S.-H.; Kim, Y.-H.; Ban, C.; Gillaspie, D. T.; Pesaran, A.

2009-05-01T23:59:59.000Z

303

PRETREATING URANIUM FOR METAL PLATING  

DOE Patents (OSTI)

A process is given for anodically treating the surface of uranium articles, prior to metal plating. The metal is electrolyzed in an aqueous solution of about 10% polycarboxylic acid, preferably oxalic acid, from 1 to 5% by weight of glycerine and from 1 to 5% by weight of hydrochloric acid at from 20 to 75 deg C for from 30 seconds to 15 minutes. A current density of from 60 to 100 amperes per square foot is used.

Wehrmann, R.F.

1961-05-01T23:59:59.000Z

304

LIQUID METAL COMPOSITIONS CONTAINING URANIUM  

DOE Patents (OSTI)

Liquid metal compositions containing a solid uranium compound dispersed therein is described. Uranium combines with tin to form the intermetallic compound USn/sub 3/. It has been found that this compound may be incorporated into a liquid bath containing bismuth and lead-bismuth components, if a relatively small percentage of tin is also included in the bath. The composition has a low thermal neutron cross section which makes it suitable for use in a liquid metal fueled nuclear reactor.

Teitel, R.J.

1959-04-21T23:59:59.000Z

305

Metal detector technology data base  

Science Conference Proceedings (OSTI)

The tests described in this report were conducted to obtain information on the effects target characteristics have on portal type metal detector response. A second purpose of the tests was to determine the effect of detector type and settings on the detection of the targets. Although in some cases comparison performance of different types and makes of metal detectors is found herein, that is not the primary purpose of the report. Further, because of the many variables that affect metal detector performance, the information presented can be used only in a general way. The results of these tests can show general trends in metal detection, but do little for making accurate predictions as to metal detector response to a target with a complex shape such as a handgun. The shape of an object and its specific metal content (both type and treatment) can have a significant influence on detection. Thus it should not be surprising that levels of detection for a small 100g stainless steel handgun are considerably different than for detection of the 100g stainless steel right circular cylinder that was used in these tests. 7 figs., 1 tab.

Porter, L.K.; Gallo, L.R.; Murray, D.W.

1990-08-01T23:59:59.000Z

306

High-Pressure Thermodynamic Properties of f-electron Metals, Transition Metal Oxides, and Half-Metallic Magnets  

SciTech Connect

This project involves research into the thermodynamic properties of f-electron metals, transition metal oxides, and half-metallic magnets at high pressure. These materials are ones in which the changing importance of electron-electron interactions as the distance between atoms is varied can tune the system through phase transitions from localized to delocalized electrons, from screened to unscreened magnetic moments, and from normal metal to one in which only a single spin specie can conduct. Three main thrusts are being pursued: (1) Mott transitions in transition metal oxides, (2) magnetism in half-metallic compounds, and (3) large volume-collapse transitions in f-band metals.

Scalettar, Richard T.; Pickett, Warren E.

2004-07-01T23:59:59.000Z

307

High-Pressure Thermodynamic Properties of f-electron Metals, Transition Metal Oxides, and Half-Metallic Magnets  

SciTech Connect

This project involves research into the thermodynamic properties of f-electron metals, transition metal oxides, and half-metallic magnets at high pressure. These materials are ones in which the changing importance of electron-electron interactions as the distance between atoms is varied can tune the system through phase transitions from localized to delocalized electrons, from screened to unscreened magnetic moments, and from normal metal to one in which only a single spin specie can conduct. Three main thrusts are being pursued: (i) Mott transitions in transition metal oxides, (ii) magnetism in half-metallic compounds, and (iii) large volume-collapse transitions in f-band metals.

Richard T. Scalettar; Warren E. Pickett

2005-08-02T23:59:59.000Z

308

Dispersion enhanced metal/zeolite catalysts  

DOE Patents (OSTI)

Dispersion stabilized zeolite supported metal catalysts are provided as bimetallic catalyst combinations. The catalyst metal is in a reduced zero valent form while the dispersion stabilizer metal is in an unreduced ionic form. Representative catalysts are prepared from platinum or nickel as the catalyst metal and iron or chromium dispersion stabilizer.

Sachtler, Wolfgang M. H. (Evanston, IL); Tzou, Ming-Shin (Evanston, IL); Jiang, Hui-Jong (Evanston, IL)

1987-01-01T23:59:59.000Z

309

Anaerobic microbial remobilization of coprecipitated metals  

DOE Patents (OSTI)

A process is provided for solubilizing coprecipitated metals. Metals in waste streams are concentrated by treatment with an iron oxide coprecipitating agent. The coprecipitated metals are solubilized by contacting the coprecipitate with a bacterial culture of a Clostridium species ATCC 53464. The remobilized metals can then be recovered and recycled. 4 figs.

Francis, A.J.; Dodge, C.J.

1994-10-11T23:59:59.000Z

310

Metal Detectives: New Book Details Titanic Investigation  

Science Conference Proceedings (OSTI)

Metal Detectives: New Book Details Titanic Investigation. For Immediate Release: April 15, 2008. ...

2012-10-02T23:59:59.000Z

311

Metal salt catalysts for enhancing hydrogen spillover  

DOE Patents (OSTI)

A composition for hydrogen storage includes a receptor, a hydrogen dissociating metal doped on the receptor, and a metal salt doped on the receptor. The hydrogen dissociating metal is configured to spill over hydrogen to the receptor, and the metal salt is configured to increase a rate of the spill over of the hydrogen to the receptor.

Yang, Ralph T; Wang, Yuhe

2013-04-23T23:59:59.000Z

312

Textured Metal Catalysts for Heterogeneous Catalysis ...  

Biomass and Biofuels Advanced Materials Textured Metal Catalysts for Heterogeneous Catalysis Pacific Northwest National Laboratory. Contact ...

313

Stabilization of Nickel Metal Catalysts for Aqueous ...  

Biomass and Biofuels Stabilization of Nickel Metal Catalysts for Aqueous Processing Systems Pacific Northwest National Laboratory.

314

Horizontal electromagnetic casting of thin metal sheets  

DOE Patents (OSTI)

Thin metal sheets are cast by magnetically suspending molten metal deposited within a ferromagnetic yoke and between AC conducting coils and linearly displacing the magnetically levitated liquid metal while it is being cooled to form a solid metal sheet. Magnetic flux increases as the molten metal sheet moves downward and decreases as the molten metal sheet moves upward to stabilize the sheet and maintain it in equilibrium as it is linearly displaced and solidified by cooling gases. A conducting shield is electrically coupled to the molten metal sheet by means of either metal sheet engaging rollers or brushes on the solidified metal, and by means of an electrode in the vessel containing the molten metal thereby providing a return path for the eddy currents induced in the metal sheet by the AC coil generated magnetic flux. Variation in the geometry of the conducting shield allows the magnetic flux between the metal sheet and the conducting shield to be varied and the thickness in surface quality of the metal sheet to be controlled. Side guards provide lateral containment for the molten metal sheet and stabilize and shape the magnetic field while a leader sheet having electromagnetic characteristics similar to those of the metal sheet is used to start the casting process and precedes the molten metal sheet through the magnet and forms a continuous sheet therewith. The magnet may be either U-shaped with a single racetrack coil or may be rectangular with a pair of facing bedstead coils.

Hull, John R. (Hinsdale, IL); Lari, Robert J. (Aurora, IL); Praeg, Walter F. (Palos Park, IL); Turner, Larry R. (Naperville, IL)

1987-01-01T23:59:59.000Z

315

Horizontal electromagnetic casting of thin metal sheets  

DOE Patents (OSTI)

Thin metal sheets are cast by magnetically suspending molten metal deposited within a ferromagnetic yoke and between AC conducting coils and linearly displacing the magnetically levitated liquid metal while it is being cooled to form a solid metal sheet. Magnetic flux increases as the molten metal sheet moves downward and decreases as the molten metal sheet moves upward to stabilize the sheet and maintain it in equilibrium as it is linearly displaced and solidified by cooling gases. A conducting shield is electrically coupled to the molten metal sheet by means of either metal sheet engaging rollers or brushes on the solidified metal, and by means of an electrode in the vessel containing the molten metal thereby providing a return path for the eddy currents induced in the metal sheet by the AC coil generated magnetic flux. Variation in the geometry of the conducting shield allows the magnetic flux between the metal sheet and the conducting shield to be varied and the thickness in surface quality of the metal sheet to be controlled. Side guards provide lateral containment for the molten metal sheet and stabilize and shape the magnetic field while a leader sheet having electromagnetic characteristics similar to those of the metal sheet is used to start the casting process and precedes the molten metal sheet through the magnet and forms a continuous sheet therewith. The magnet may be either U-shaped with a single racetrack coil or may be rectangular with a pair of facing bedstead coils.

Hull, John R. (Hinsdale, IL); Lari, Robert J. (Aurora, IL); Praeg, Walter F. (Palos Park, IL); Turner, Larry R. (Naperville, IL)

1988-01-01T23:59:59.000Z

316

Materials Design of Advanced Performance Metal Catalysts  

SciTech Connect

The contribution of materials design to the fabrication of advanced metal catalysts is highlighted, with particular emphasis on the construction of relatively complex contact structures surrounding metal nanoparticles. Novel advanced metal catalysts can be synthesized via encapsulation of metal nanoparticles into oxide shells, immobilization of metal oxide core-shell structures on solid supports, post-modification of supported metal nanoparticles by surface coating, and premodification of supports before loading metal nanoparticles. Examples on how these materials structures lead to enhanced catalytic performance are illustrated, and a few future prospects are presented.

Ma, Zhen [ORNL; Dai, Sheng [ORNL

2008-01-01T23:59:59.000Z

317

Inert anode containing base metal and noble metal useful for the electrolytic production of aluminum  

DOE Patents (OSTI)

An inert anode for production of metals such as aluminum is disclosed. The inert anode comprises a base metal selected from Cu and Ag, and at least one noble metal selected from Ag, Pd, Pt, Au, Rh, Ru, Ir and Os. The inert anode may optionally be formed of sintered particles having interior portions containing more base metal than noble metal and exterior portions containing more noble metal than base metal. In a preferred embodiment, the base metal comprises Cu, and the noble metal comprises Ag, Pd or a combination thereof.

Ray, Siba P. (Murrysville, PA); Liu, Xinghua (Monroeville, PA)

2000-01-01T23:59:59.000Z

318

Process for fabrication of metal oxide films  

DOE Patents (OSTI)

This invention is comprised of a method of fabricating metal oxide films from a plurality of reactants by inducing a reaction by plasma deposition among the reactants. The plasma reaction is effective for consolidating the reactants and producing thin films of metal oxides, e.g. electro-optically active transition metal oxides, at a high deposition rate. The presence of hydrogen during the plasma reaction enhances the deposition rate of the metal oxide. Various types of metal oxide films can be produced.

Tracy, C.E.; Benson, D.; Svensson, S.

1990-07-17T23:59:59.000Z

319

Semiconductor assisted metal deposition for nanolithography applications  

DOE Patents (OSTI)

An article of manufacture and method of forming nanoparticle sized material components. A semiconductor oxide substrate includes nanoparticles of semiconductor oxide. A modifier is deposited onto the nanoparticles, and a source of metal ions are deposited in association with the semiconductor and the modifier, the modifier enabling electronic hole scavenging and chelation of the metal ions. The metal ions and modifier are illuminated to cause reduction of the metal ions to metal onto the semiconductor nanoparticles.

Rajh, Tijana (Naperville, IL); Meshkov, Natalia (Downers Grove, IL); Nedelijkovic, Jovan M. (Belgrade, YU); Skubal, Laura R. (West Brooklyn, IL); Tiede, David M. (Elmhurst, IL); Thurnauer, Marion (Downers Grove, IL)

2002-01-01T23:59:59.000Z

320

Reversible photodeposition and dissolution of metal ions  

DOE Patents (OSTI)

A cyclic photocatalytic process for treating waste water containing metal and organic contaminants. In one embodiment of the method, metal ions are photoreduced onto the photocatalyst and the metal concentrated by resolubilization in a smaller volume. In another embodiment of the method, contaminant organics are first oxidized, then metal ions removed by photoreductive deposition. The present invention allows the photocatalyst to be recycled until nearly complete removal of metal ions and organic contaminants is achieved.

Foster, Nancy S. (Boulder, CO); Koval, Carl A. (Golden, CO); Noble, Richard D. (Boulder, CO)

1994-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

Coated Metal Articles and Method of Making  

DOE Patents (OSTI)

The method of protectively coating metallic uranium which comprises dipping the metallic uranium in a molten alloy comprising about 20-75% of copper and about 80-25% of tin, dipping the coated uranium promptly into molten tin, withdrawing it from the molten tin and removing excess molten metal, thereupon dipping it into a molten metal bath comprising aluminum until it is coated with this metal, then promptly withdrawing it from the bath.

Boller, Ernest R.; Eubank, Lowell D.

2004-07-06T23:59:59.000Z

322

Zone refining of plutonium metal  

Science Conference Proceedings (OSTI)

The zone refining process was applied to Pu metal containing known amounts of impurities. Rod specimens of plutonium metal were melted into and contained in tantalum boats, each of which was passed horizontally through a three-turn, high-frequency coil in such a manner as to cause a narrow molten zone to pass through the Pu metal rod 10 times. The impurity elements Co, Cr, Fe, Ni, Np, U were found to move in the same direction as the molten zone as predicted by binary phase diagrams. The elements Al, Am, and Ga moved in the opposite direction of the molten zone as predicted by binary phase diagrams. As the impurity alloy was zone refined, {delta}-phase plutonium metal crystals were produced. The first few zone refining passes were more effective than each later pass because an oxide layer formed on the rod surface. There was no clear evidence of better impurity movement at the slower zone refining speed. Also, constant or variable coil power appeared to have no effect on impurity movement during a single run (10 passes). This experiment was the first step to developing a zone refining process for plutonium metal.

Blau, M.S.

1994-08-01T23:59:59.000Z

323

Advances in metallic nuclear fuel  

Science Conference Proceedings (OSTI)

Metallic nuclear fuels have generated renewed interest for advanced liquid metal reactors (LMRs) due to their physical properties, ease of fabrication, irradiation behavior, and simple reprocessing. Irradiation performance for both steady-state and transient operations is excellent. Ongoing irradiation tests in Argonne-West's Idaho-based Experimental Breeder Reactor II (EBR-II) have surpassed 100,000 MWd/T burnup and are on their way to a lifetime burnup of 150,000 MWd/T or greater. Metallic fuel also has a unique neutronic characteristic that enables benign reactor responses to loss-of-flow without scram and loss-of-heat-sink without scram accident conditions. This inherent safety potential of metallic fuel was demonstrated in EBR-II just one year ago. Safety tests performed in the reactor have also demonstrated that there is ample margin to fuel element cladding failure under transient overpower conditions. These metallic fuel attributes are key ingredients of the integral fast reactor (IFR) concept being developed at Argonne National Laboratory.

Seidel, B.R.; Walters, L.C.; Chang, Y.I.

1987-04-01T23:59:59.000Z

324

THE LIQUID METAL LINEAR GENERATOR  

SciTech Connect

In the utilization of nuclear heat energy, liquid metal could be used in a vapor cycle to propel a column of liquid metal in a jet pump or injector where electrical energy could be extracted by means of a MHD arrangement. The recirculating system is being studied as a means of increasing the efficiency. Results are described briefly for a preliminary run made using steam and water; the efficiency of conversion of steam kinetic energy to liquid kinetic energy was approximates 20%. The possible causes of the low efficiency and some of the methods for decreasing hydraulic losses are outlined. (D.L.C.)

Sowa, E.S.

1963-10-31T23:59:59.000Z

325

Cerenkov radiation in metallic metamaterials  

SciTech Connect

The electromagnetic response of a metallic metamaterial to fast-moving electrons is studied by numerical simulations. The considered metamaterial is a one-dimensional array of slits perforated on a metallic film and is found to generate Cerenkov wakes when the electron beam travels near its surface. There is no energy threshold for the generation of such wakes, which would be promising to lower the operation energy of the electron beam in compact Cerenkov free-electron-lasers. Moreover, by analyzing the spectral dependence of the Cerenkov light, it is possible to map the dispersion relation of the guided modes supported by the metamaterial.

So, Jin-Kyu; Won, Jong-Hyo; Sattorov, M. A.; Bak, Seung-Ho; Jang, Kyu-Ha; Park, Gun-Sik [Department of Physics and Astronomy, Center for THz-Bio Application Systems, Seoul National University, Seoul 151-747 (Korea, Republic of); Kim, D. S. [Department of Physics and Astronomy, Center for Subwavelength Optics, Seoul National University, Seoul 151-747 (Korea, Republic of); Garcia-Vidal, F. J. [Departamento de Fisica Teorica de la Materia Condensada, Universidad Autonoma de Madrid, E-28049 Madrid (Spain)

2010-10-11T23:59:59.000Z

326

METHOD OF CLEANING METAL SURFACES  

DOE Patents (OSTI)

Cleaning fluids for removing deposits from metal surfaces are described. The cleaning agents of the invention consist of aqueous nitric acid and an amhydrous nitrate salt of a metal which is lower in the electromotive series than the element of the deposit to be removed. In general, the salt content of thc cleaning agents ranged from 10 to 90%, preferably from 10 to 40% by weight; and the balance of the composition comprises nitric acid of any strength from extremely dilute up to concentrated strength.

Winkler, H.W.; Morfitt, J.W.; Little, T.H.

1959-05-19T23:59:59.000Z

327

Thin films of mixed metal compounds  

DOE Patents (OSTI)

Disclosed is a thin film heterojunction solar cell, said heterojunction comprising a p-type I-III-IV[sub 2] chalcopyrite substrate and an overlying layer of an n-type ternary mixed metal compound wherein said ternary mixed metal compound is applied to said substrate by introducing the vapor of a first metal compound to a vessel containing said substrate from a first vapor source while simultaneously introducing a vapor of a second metal compound from a second vapor source of said vessel, said first and second metals comprising the metal components of said mixed metal compound; independently controlling the vaporization rate of said first and second vapor sources; reducing the mean free path between vapor particles in said vessel, said gas being present in an amount sufficient to induce homogeneity of said vapor mixture; and depositing said mixed metal compound on said substrate in the form of a uniform composition polycrystalline mixed metal compound. 5 figs.

Mickelsen, R.A.; Chen, W.S.

1985-06-11T23:59:59.000Z

328

Metal-On-Metal Bonding and Rebonding Revisited  

SciTech Connect

Density-functional calculations for a wide variety of metals show that, contrary to the rebonding view of adsorbate bonding, addimers do not have notably longer surface bonds than adatoms, do not reside farther above the surface, and do not meet the rebonding arguments for augmented mobility. Rebonding concepts are found to have some utility in explaining addimer stability.

Bogicevic, A.

1999-02-23T23:59:59.000Z

329

Data:89f6d69a-85f5-4a51-936d-0f72768c0a56 | Open Energy Information  

Open Energy Info (EERE)

9f6d69a-85f5-4a51-936d-0f72768c0a56 9f6d69a-85f5-4a51-936d-0f72768c0a56 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Nueces Electric Coop, Inc Effective date: 2009/11/20 End date if known: Rate name: Security/Street Light Service- 1000w MH Sector: Lighting Description: *Security/Street Light Service is available to Members, municipalities and governmental authorities in accordance with the Cooperative's Service Rules and Regulations for pole mounted area security and street lighting near the Cooperative's electric distribution lines with existing transformers. MV = Mercury Vapor; HPS = High Pressure Sodium; MH = Metal Halide; X= Cobra Head assembly.

330

Metal oxide and metal fluoride nanostructures and methods of making same  

SciTech Connect

The present invention includes pure single-crystalline metal oxide and metal fluoride nanostructures, and methods of making same. These nanostructures include nanorods and nanoarrays.

Wong, Stanislaus S. (Stony Brook, NY); Mao, Yuanbing (Los Angeles, CA)

2009-08-18T23:59:59.000Z

331

Thermal barrier and overlay coating systems comprising composite metal/metal oxide bond coating layers  

DOE Patents (OSTI)

The present invention generally describes multilayer coating systems comprising a composite metal/metal oxide bond coat layer. The coating systems may be used in gas turbines.

Goedjen, John G. (Oviedo, FL); Sabol, Stephen M. (Orlando, FL); Sloan, Kelly M. (Longwood, FL); Vance, Steven J. (Orlando, FL)

2001-01-01T23:59:59.000Z

332

Stabilization of Electrocatalytic Metal Nanoparticles at Metal-Metal Oxide-Graphene Triple Junction Points  

DOE Green Energy (OSTI)

Carbon-supported metal catalysts are widely used in heterogeneous catalysis and electrocatalysis. In this paper, we report a novel method to deposit metal catalysts and metal oxide nanoparticles on two-dimensional graphene sheets to improve the catalytic performance and stability of the catalyst materials. The new synthesis method allows indium tin oxide (ITO) nanocrystals to be directly grown on functionalized graphene sheets forming the ITO-graphene hybrids. Pt nanoparticles are then deposited to form a special triple-junction structure (Pt-ITO-graphene). Both experimental study and periodic density functional theory calculations show that the supported Pt nanoparticles are stable at Pt-ITO-graphene triple junction points. The new catalyst materials were tested for oxygen reduction for potential applications in polymer electrolyte membrane fuel cells, and they exhibited greatly enhanced stability and activity. The reasons for the high stability and activity of Pt-ITO-graphene are analyzed.

Kou, Rong; Shao, Yuyan; Mei, Donghai; Nie, Zimin; Wang, Donghai; Wang, Chong M.; Viswanathan, Vilayanur V.; Park, Seh K.; Aksay, Ilhan A.; Lin, Yuehe; Wang, Yong; Liu, Jun

2011-03-02T23:59:59.000Z

333

Transition metal sulfide loaded catalyst  

DOE Patents (OSTI)

A zeolite based catalyst for activation and conversion of methane. A zeolite support includes a transition metal (Mo, Cr or W) sulfide disposed within the micropores of the zeolite. The catalyst allows activation and conversion of methane to C.sub.2 + hydrocarbons in a reducing atmosphere, thereby avoiding formation of oxides of carbon.

Maroni, Victor A. (Naperville, IL); Iton, Lennox E. (Downers Grove, IL); Pasterczyk, James W. (Westmont, IL); Winterer, Markus (Westmont, IL); Krause, Theodore R. (Lisle, IL)

1994-01-01T23:59:59.000Z

334

Transition metal sulfide loaded catalyst  

DOE Patents (OSTI)

A zeolite-based catalyst is described for activation and conversion of methane. A zeolite support includes a transition metal (Mo, Cr or W) sulfide disposed within the micropores of the zeolite. The catalyst allows activation and conversion of methane to C[sub 2]+ hydrocarbons in a reducing atmosphere, thereby avoiding formation of oxides of carbon.

Maroni, V.A.; Iton, L.E.; Pasterczyk, J.W.; Winterer, M.; Krause, T.R.

1994-04-26T23:59:59.000Z

335

Machinable dissolved metal oxide superconductors  

DOE Patents (OSTI)

Powders of a metal oxide superconductor are mixed with sufficient amount (10--80 mol%) of In, Sn, and/or Al, to become nonbrittle, machinable. Preferred superconductors are YBa[sub 2]Cu[sub 3]O[sub 7[minus]x] and Bi-Sr-Ca-Cu-O compounds.

Chen, Chung-Hsuan.

1991-01-01T23:59:59.000Z

336

Corrosion resistant metallic bipolar plate  

SciTech Connect

A corrosion resistant, electrically conductive component such as a bipolar plate for a PEM fuel cell includes 20 55% Cr, balance base metal such as Ni, Fe, or Co, the component having thereon a substantially external, continuous layer of chromium nitride.

Brady, Michael P. (Oak Ridge, TN); Schneibel, Joachim H. (Knoxville, TN); Pint, Bruce A. (Knoxville, TN); Maziasz, Philip J. (Oak Ridge, TN)

2007-05-01T23:59:59.000Z

337

Machinable dissolved metal oxide superconductors  

DOE Patents (OSTI)

Powders of a metal oxide superconductor are mixed with sufficient amount (10--80 mol%) of In, Sn, and/or Al, to become nonbrittle, machinable. Preferred superconductors are YBa{sub 2}Cu{sub 3}O{sub 7{minus}x} and Bi-Sr-Ca-Cu-O compounds.

Chen, Chung-Hsuan

1991-12-31T23:59:59.000Z

338

Hydrothermal alkali metal catalyst recovery process  

DOE Patents (OSTI)

In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles primarily in the form of water soluble alkali metal formates by treating the particles with a calcium or magnesium-containing compound in the presence of water at a temperature between about 250.degree. F. and about 700.degree. F. and in the presence of added carbon monoxide. During the treating process the water insoluble alkali metal compounds comprising the insoluble alkali metal residues are converted into water soluble alkali metal formates. The resultant aqueous solution containing water soluble alkali metal formates is then separated from the treated particles and any insoluble materials formed during the treatment process, and recycled to the gasification process where the alkali metal formates serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. This process permits increased recovery of alkali metal constituents, thereby decreasing the overall cost of the gasification process by reducing the amount of makeup alkali metal compounds necessary.

Eakman, James M. (Houston, TX); Clavenna, LeRoy R. (Baytown, TX)

1979-01-01T23:59:59.000Z

339

Recipient: The 2005 LMD Light Metals Technical Service Award - TMS  

Science Conference Proceedings (OSTI)

The Minerals, Metals & Materials Society's Light Metals Division's Light Metals Technical Service Award, established in 1995, recognizes an individual who has ...

340

Trace Metals in Oil Laboratory Proficiency Program  

Science Conference Proceedings (OSTI)

Lab Proficiency Testing service for Trace Metals in Oil. Soybean oil sample to test for Iron, Copper, and Nickel using AOCS Official method Ca 18-79. Trace Metals in Oil Laboratory Proficiency Program Laboratory Proficiency Program (LPP) aocs applicants

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

Metal Silicides: An Integral Part of Microelectronics  

Science Conference Proceedings (OSTI)

Metal silicide thin films are integral parts of all microelectronics devices. .... with activation energy around 11.5 eV for refractory metal/silicon systems and 0.5 eV

342

CORROSION OF METALS IN OIL SHALE ENVIRONMENTS  

E-Print Network (OSTI)

CORROSION OF METALS IN OIL SHALE ENVIRONMENTS A. Levy and R.of Metals in In-Situ Oil Shale Retorts," NACE Corrosion 80,Elevated Temperature Corrosion of Oil Shale Retort Component

Bellman Jr., R.

2012-01-01T23:59:59.000Z

343

Gas adsorption on metal-organic frameworks  

SciTech Connect

The present invention involves the use of certain metal organic frameworks that have been treated with water or another metal titrant in the storage of carbon dioxide. The capacity of these frameworks is significantly increased through this treatment.

Willis, Richard R. (Cary, IL); Low, John J. (Schaumburg, IL), Faheem, Syed A. (Huntley, IL); Benin, Annabelle I. (Oak Forest, IL); Snurr, Randall Q. (Evanston, IL); Yazaydin, Ahmet Ozgur (Evanston, IL)

2012-07-24T23:59:59.000Z

344

CORROSION OF METALS IN OIL SHALE ENVIRONMENTS  

E-Print Network (OSTI)

CORROSION OF METALS IN OIL SHALE ENVIRONMENTS A. Levy and R.of Metals in In-Situ Oil Shale Retorts," NACE Corrosion 80,Corrosion of Oil Shale Retort Component Materials," LBL-

Bellman Jr., R.

2012-01-01T23:59:59.000Z

345

Liquid-metal embrittlement of refractory metals by molten plutonium  

Science Conference Proceedings (OSTI)

Embrittlement by molten plutonium of the refractory metals and alloys W-25 wt % Re, tantalum, molybdenum, and Ta-10 wt % W was studied. At 900/sup 0/C and a strain rate of 10/sup -4/ s/sup -1/, the materials tested may be ranked in order of decreasing susceptibility to liquid-plutonium embrittlement as follows: molybdenum, W-25 wt % Re, Ta-10 wt % W, and tantalum. These materials exhibited a wide range in susceptibility. Embrittlement was found to exhibit a high degree of temperature and strain-rate dependence, and we present arguments that strongly support a stress-assisted, intergranular, liquid-metal corrosion mechanism. We also believe microstructure plays a key role in the extent of embrittlement. In the case of W-25 wt % Re, we have determined that a dealloying corrosion takes place in which rhenium is selectively withdrawn from the alloy.

Lesuer, D.R.; Bergin, J.B.; McInturff, S.A.; Kuhn, B.A.

1980-07-01T23:59:59.000Z

346

Fabrication of Metal Foam and its Applications  

Science Conference Proceedings (OSTI)

Mechanical and Physical Properties of Roof Tile Manufacturing from Red Mud ... Structural Engineering of Semiconductor Layered Metal Oxides for Solar...

347

Underpotential Dissolution of Precious Metals from Intermetallic ...  

Science Conference Proceedings (OSTI)

Abstract Scope, The dissolution of precious metals (PMs) can be enhanced by ... during Copper Electrowinning using the Galvanostatic Staircase Method.

348

Metal-Matrix Composites for Space Applications  

Science Conference Proceedings (OSTI)

... advancements were made on the fundamental science and technology front, ... Suplinskas, Continuous Boron Fiber MMC's, Engineered Metal Handbook,...

349

Nanocrystalline and Nanotwinned Metals under Extreme Environment  

Science Conference Proceedings (OSTI)

The applicability of nanostructured metals under extreme environment (high temperature, ... of Transport Phenomena for Enhanced Oil Recovery Applications .

350

CR3 Update: Recycling of Strategic Metals  

Science Conference Proceedings (OSTI)

Apr 20, 2012 ... Education and Certifications, Expand Education and Certifications .... However, some other industrially significant metals indicate higher...

351

Recipients: The 1998 LMD Light Metals Award  

Science Conference Proceedings (OSTI)

Paper Title: "Coalescence Behaviour of Aluminum Droplets under Molten Salt Flux Cover," in Light Metals 1997, edited by Barry Welch.

352

Dendrite Growth Prevention Technology for Lithium Metal ...  

Search PNNL. PNNL Home; About; Research; Publications; Jobs; News; Contacts; Dendrite Growth Prevention Technology for Lithium Metal Batteries. ...

353

Slip and Slip Traces in BCC Metals  

Science Conference Proceedings (OSTI)

Additional examination by scanning electron microscopy allowed the ... Calculation of Defect Stability and Mobility in High-temperature BCC Metals.

354

Method for decontamination of radioactive metal surfaces  

DOE Patents (OSTI)

Disclosed is a method for removing radioactive contaminants from metal surfaces by applying steam containing an inorganic acid and cerium IV. Cerium IV is applied to contaminated metal surfaces by introducing cerium IV in solution into a steam spray directed at contaminated metal surfaces. Cerium IV solution is converted to an essentially atomized or vapor phase by the steam.

Bray, Lane A. (Richland, WA)

1996-01-01T23:59:59.000Z

355

TREATMENT OF METALS PRIOR TO ELECTROPLATING  

DOE Patents (OSTI)

The preparation of certain metal surfaces to receive electrodeposits is described. Surfaces of the metals are subjected to shot blasting by ferrous metal shot, and the surfaces then are given a coating of copper by displacement from a copper salt solution. The method applies to U, Zr, Ti, Ta, Ni, Mo, W, and V.

Huddle, R.A.U.; Flint, O.

1958-05-20T23:59:59.000Z

356

Thin films of mixed metal compounds  

DOE Patents (OSTI)

A compositionally uniform thin film of a mixed metal compound is formed by simultaneously evaporating a first metal compound and a second metal compound from independent sources. The mean free path between the vapor particles is reduced by a gas and the mixed vapors are deposited uniformly. The invention finds particular utility in forming thin film heterojunction solar cells.

Mickelsen, Reid A. (Bellevue, WA); Chen, Wen S. (Seattle, WA)

1985-01-01T23:59:59.000Z

357

Multifunctional heterostructures comprised of carbon and metal ...  

Science Conference Proceedings (OSTI)

Register as a New User ... from thin metal films, and further oxidized to create a thin surface oxide shell. ... were demonstrated as a unique plasmonic substrates and catalytic substrates. This approach of graphene shells growth around noble metal nanoparticles ... Novel Methods of Synthesis of Metal Oxide Nanoparticles.

358

Ammonia release method for depositing metal oxides  

DOE Patents (OSTI)

A method of depositing metal oxides on substrates which is indifferent to the electrochemical properties of the substrates and which comprises forming ammine complexes containing metal ions and thereafter effecting removal of ammonia from the ammine complexes so as to permit slow precipitation and deposition of metal oxide on the substrates.

Silver, G.L.; Martin, F.S.

1993-12-31T23:59:59.000Z

359

Process for making transition metal nitride whiskers  

DOE Patents (OSTI)

A process for making metal nitrides, particularly titanium nitride whiskers, using a cyanide salt as a reducing agent for a metal compound in the presence of an alkali metal oxide. Sodium cyanide, various titanates and titanium oxide mixed with sodium oxide react to provide titanium nitride whiskers that can be used as reinforcement to ceramic composites. 1 fig., 1 tab.

Bamberger, C.E.

1988-04-12T23:59:59.000Z

360

Method for decontamination of radioactive metal surfaces  

DOE Patents (OSTI)

Disclosed is a method for removing radioactive contaminants from metal surfaces by applying steam containing an inorganic acid and cerium IV. Cerium IV is applied to contaminated metal surfaces by introducing cerium IV in solution into a steam spray directed at contaminated metal surfaces. Cerium IV solution is converted to an essentially atomized or vapor phase by the steam.

Bray, L.A.

1996-08-13T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

An integrated decontamination process for metals  

DOE Patents (OSTI)

An integrated process for decontamination of metals, particularly metals that are used in the nuclear energy industry contaminated with radioactive material. The process combines the processes of electrorefining and melt refining to purify metals that can be decontaminated using either electrorefining or melt refining processes.

Snyder, T.S.; Whitlow, G.A.

1989-06-08T23:59:59.000Z

362

Synthesis of transition metal carbonitrides  

DOE Patents (OSTI)

Transition metal carbonitrides (in particular, titanium carbonitride, TiC.sub.0.5 N.sub.0.5) are synthesized by a self-propagating reaction between the metal (e.g., titanium) and carbon in a nitrogen atmosphere. Complete conversion to the carbonitride phase is achieved with the addition of TiN as diluent and with a nitrogen pressure .gtoreq.0.6 MPa. Thermodynamic phase-stability calculations and experimental characterizations of quenched samples provided revealed that the mechanism of formation of the carbonitride is a two-step process. The first step involves the formation of the nonstoichiometric carbide, TiC.sub.0.5, and is followed by the formation of the product by the incorporation of nitrogen in the defect-structure carbide.

Munir, Zuhair A. R. (Davis, CA); Eslamloo-Grami, Maryam (Davis, CA)

1994-01-01T23:59:59.000Z

363

Sulfuryl Halide -Based Ultralow Temperature Primary Batteries  

Science Conference Proceedings (OSTI)

Hot Section Corrosion Issues in Microturbines Operating on B100 Bio-Diesel Impact of Impurities and ... Large-Scale Technique for Dye Solar Cells Preparation.

364

Metal-air battery assessment  

DOE Green Energy (OSTI)

The objective of this report is to evaluate the present technical status of the zinc-air, aluminum/air and iron/air batteries and assess their potential for use in an electric vehicle. In addition, this report will outline proposed research and development priorities for the successful development of metal-air batteries for electric vehicle application. 39 refs., 25 figs., 11 tabs.

Sen, R.K.; Van Voorhees, S.L.; Ferrel, T.

1988-05-01T23:59:59.000Z

365

Cryogenic Treatment of Metal Parts  

SciTech Connect

Cryogenic treatment and its variables have been described. Results of eight engineering tests carried out on cryotreated parts have been presented. Cryogenic treatment of metal parts enhances useful properties which in turn, improves various strengths. Our tests viz. Abrasion, Torsion, Fatigue, Tensile, Shear, Hardness and Impact on Mild steel, Cast Iron, Brass and Copper show that the cryogenic treatment improved useful properties of mild steel parts appreciably but did not show promise with brass and copper parts.

Chillar, Rahul [S. P. College of Engineering, Andheri (W), Mumbai - 400 058 (India); Agrawal, S. C. [Tata Institute of Fundamental Research, Colaba, Mumbai - 400 005 (India)

2006-03-31T23:59:59.000Z

366

Alkali metal/sulfur battery  

SciTech Connect

Alkali metal/sulfur batteries in which the electrolyte-separator is a relatively fragile membrane are improved by providing means for separating the molten sulfur/sulfide catholyte from contact with the membrane prior to cooling the cell to temperatures at which the catholyte will solidify. If the catholyte is permitted to solidify while in contact with the membrane, the latter may be damaged. The improvement permits such batteries to be prefilled with catholyte and shipped, at ordinary temperatures.

Anand, Joginder N. (Clayton, CA)

1978-01-01T23:59:59.000Z

367

PROCESS FOR PREPARING URANIUM METAL  

DOE Patents (OSTI)

A process is presented for producing oxygen-free uranium metal comprising contacting iodine vapor with crude uranium in a reaction zone maintained at 400 to 800 C to produce a vaporous mixture of UI/sub 4/ and iodine. Also disposed within the maction zone is a tungsten filament which is heated to about 1600 C. The UI/sub 4/, upon contacting the hot filament, is decomposed to molten uranium substantially free of oxygen.

Prescott, C.H. Jr.; Reynolds, F.L.

1959-01-13T23:59:59.000Z

368

Amorphous metal alloy and composite  

DOE Patents (OSTI)

Amorphous metal alloys of the iron-chromium and nickel-chromium type have excellent corrosion resistance and high temperature stability and are suitable for use as a protective coating on less corrosion resistant substrates. The alloys are stabilized in the amorphous state by one or more elements of titanium, zirconium, hafnium, niobium, tantalum, molybdenum, and tungsten. The alloy is preferably prepared by sputter deposition.

Wang, Rong (Richland, WA); Merz, Martin D. (Richland, WA)

1985-01-01T23:59:59.000Z

369

Directly susceptible, noncarbon metal ceramic composite crucible  

DOE Patents (OSTI)

A sintered metal ceramic crucible suitable for high temperature induction melting of reactive metals without appreciable carbon or silicon contamination of the melt. The crucible comprises a cast matrix of a thermally conductive ceramic material; a perforated metal sleeve, which serves as a susceptor for induction heating of the crucible, embedded within the ceramic cast matrix; and a thermal-shock-absorber barrier interposed between the metal sleeve and the ceramic cast matrix to allow for differential thermal expansions between the matrix and the metal sleeve and to act as a thermal-shock-absorber which moderates the effects of rapid changes of sleeve temperature on the matrix.

Holcombe, Jr., Cressie E. (Farragut, TN); Kiggans, Jr., James O. (Oak Ridge, TN); Morrow, S. Marvin (Kingston, TN); Rexford, Donald (Pattersonville, NY)

1999-01-01T23:59:59.000Z

370

Dose Rates from Plutonium Metal and Beryllium Metal in a 9975 Shipping Container  

SciTech Connect

A parametric study was performed of the radiation dose rates that might be produced if plutonium metal and beryllium metal were shipped in the 9975 shipping package. These materials consist of heterogeneous combinations plutonium metal and beryllium. The plutonium metal content varies up to 4.4 kilograms while the beryllium metal varies up to 4 kilograms. This paper presents the results of that study.

Nathan, S.J.

2002-02-04T23:59:59.000Z

371

Solar Thermal Electrolytic Production of Metals from Their Oxides  

Science Conference Proceedings (OSTI)

Symposium, Alternative Energy Resources for Metals and Materials Production Symposium. Presentation Title, Solar Thermal Electrolytic Production of Metals...

372

The Making and Mechanical Performance of Metal Powder Injection ...  

Science Conference Proceedings (OSTI)

Symposium, Metal and Polymer Matrix Composites ... Fabrication of Metal Matrix Composites via Spark Plasma Sintering for Nuclear Energy Application.

373

Metal resistance sequences and transgenic plants  

DOE Patents (OSTI)

The present invention provides nucleic acid sequences encoding a metal ion resistance protein, which are expressible in plant cells. The metal resistance protein provides for the enzymatic reduction of metal ions including but not limited to divalent Cu, divalent mercury, trivalent gold, divalent cadmium, lead ions and monovalent silver ions. Transgenic plants which express these coding sequences exhibit increased resistance to metal ions in the environment as compared with plants which have not been so genetically modified. Transgenic plants with improved resistance to organometals including alkylmercury compounds, among others, are provided by the further inclusion of plant-expressible organometal lyase coding sequences, as specifically exemplified by the plant-expressible merB coding sequence. Furthermore, these transgenic plants which have been genetically modified to express the metal resistance coding sequences of the present invention can participate in the bioremediation of metal contamination via the enzymatic reduction of metal ions. Transgenic plants resistant to organometals can further mediate remediation of organic metal compounds, for example, alkylmetal compounds including but not limited to methyl mercury, methyl lead compounds, methyl cadmium and methyl arsenic compounds, in the environment by causing the freeing of mercuric or other metal ions and the reduction of the ionic mercury or other metal ions to the less toxic elemental mercury or other metals.

Meagher, Richard Brian (Athens, GA); Summers, Anne O. (Athens, GA); Rugh, Clayton L. (Athens, GA)

1999-10-12T23:59:59.000Z

374

Apparatus for gas-metal arc deposition  

DOE Patents (OSTI)

Apparatus for gas-metal arc deposition of metal, metal alloys, and metal matrix composites. The apparatus contains an arc chamber for confining a D.C. electrical arc discharge, the arc chamber containing an outlet orifice in fluid communication with a deposition chamber having a deposition opening in alignment with the orifice for depositing metal droplets on a coatable substrate. Metal wire is passed continuously into the arc chamber in alignment with the orifice. Electric arcing between the metal wire anode and the orifice cathode produces droplets of molten metal from the wire which pass through the orifice and into the deposition chamber for coating a substrate exposed at the deposition opening. When producing metal matrix composites, a suspenion of particulates in an inert gas enters the deposition chamber via a plurality of feed openings below and around the orifice so that reinforcing particulates join the metal droplets to produce a uniform mixture which then coats the exposed substrate with a uniform metal matrix composite.

Buhrmaster, Carol L. (Corning, NY); Clark, Denis E. (Idaho Falls, ID); Smartt, Herschel B. (Idaho Falls, ID)

1991-01-01T23:59:59.000Z

375

Method for gas-metal arc deposition  

DOE Patents (OSTI)

Method and apparatus for gas-metal arc deposition of metal, metal alloys, and metal matrix composites. The apparatus contains an arc chamber for confining a D.C. electrical arc discharge, the arc chamber containing an outlet orifice in fluid communication with a deposition chamber having a deposition opening in alignment wiht the orifice for depositing metal droplets on a coatable substrate. Metal wire is passed continuously into the arc chamber in alignment with the orifice. Electric arcing between the metal wire anode and the orifice cathode produces droplets of molten metal from the wire which pass through the orifice and into the deposition chamber for coating a substrate exposed at the deposition opening. When producing metal matrix composites, a suspension of particulates in an inert gas enters the deposition chamber via a plurality of feed openings below and around the orifice so that reinforcing particulates join the metal droplets to produce a uniform mixture which then coats the exposed substrate with a uniform metal matrix composite.

Buhrmaster, Carol L. (Corning, NY); Clark, Denis E. (Idaho Falls, ID); Smartt, Herschel B. (Idaho Falls, ID)

1990-01-01T23:59:59.000Z

376

Method for gas-metal arc deposition  

DOE Patents (OSTI)

Method and apparatus for gas-metal arc deposition of metal, metal alloys, and metal matrix composites are disclosed. The apparatus contains an arc chamber for confining a D.C. electrical arc discharge, the arc chamber containing an outlet orifice in fluid communication with a deposition chamber having a deposition opening in alignment with the orifice for depositing metal droplets on a coatable substrate. Metal wire is passed continuously into the arc chamber in alignment with the orifice. Electric arcing between the metal wire anode and the orifice cathode produces droplets of molten metal from the wire which pass through the orifice and into the deposition chamber for coating a substrate exposed at the deposition opening. When producing metal matrix composites, a suspension of particulates in an inert gas enters the deposition chamber via a plurality of feed openings below and around the orifice so that reinforcing particulates join the metal droplets to produce a uniform mixture which then coats the exposed substrate with a uniform metal matrix composite. 1 fig.

Buhrmaster, C.L.; Clark, D.E.; Smartt, H.B.

1990-11-13T23:59:59.000Z

377

Ravi Metallics Ltd | Open Energy Information  

Open Energy Info (EERE)

Metallics Ltd Metallics Ltd Jump to: navigation, search Name Ravi Metallics Ltd. Place Rourkela, Orissa, India Zip 769004 Sector Biomass Product Rourkela-based biomass project developer. References Ravi Metallics Ltd.[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Ravi Metallics Ltd. is a company located in Rourkela, Orissa, India . References ↑ "Ravi Metallics Ltd." Retrieved from "http://en.openei.org/w/index.php?title=Ravi_Metallics_Ltd&oldid=350202" Categories: Clean Energy Organizations Companies Organizations Stubs What links here Related changes Special pages Printable version Permanent link Browse properties 429 Throttled (bot load) Error 429 Throttled (bot load)

378

Method of nitriding refractory metal articles  

DOE Patents (OSTI)

A method of nitriding a refractory-nitride forming metal or metalloid articles and composite articles. A consolidated metal or metalloid article or composite is placed inside a microwave oven and nitrogen containing gas is introduced into the microwave oven. The metal or metalloid article or composite is heated to a temperature sufficient to react the metal or metalloid with the nitrogen by applying a microwave energy within the microwave oven. The metal or metalloid article or composite is maintained at that temperature for a period of time sufficient to convert the article of metal or metalloid or composite to an article or composite of refractory nitride. In addition, a method of applying a coating, such as a coating of an oxide, a carbide, or a carbo-nitride, to an article of metal or metalloid by microwave heating.

Tiegs, Terry N. (Lenoir City, TN); Holcombe, Cressie E. (Knoxville, TN); Dykes, Norman L. (Oak Ridge, TN); Omatete, Ogbemi O. (Lagos, NG); Young, Albert C. (Flushing, NY)

1994-01-01T23:59:59.000Z

379

Method of nitriding refractory metal articles  

DOE Patents (OSTI)

A method of nitriding a refractory-nitride forming metal or metalloid articles and composite articles. A consolidated metal or metalloid article or composite is placed inside a microwave oven and nitrogen containing gas is introduced into the microwave oven. The metal or metalloid article or composite is heated to a temperature sufficient to react the metal or metalloid with the nitrogen by applying a microwave energy within the microwave oven. The metal or metalloid article or composite is maintained at that temperature for a period of time sufficient to convert the article of metal or metalloid or composite to an article or composite of refractory nitride. In addition, a method of applying a coating, such as a coating of an oxide, a carbide, or a carbo-nitride, to an article of metal or metalloid by microwave heating.

Tiegs, T.N.; Holcombe, C.E.; Dykes, N.L.; Omatete, O.O.; Young, A.C.

1994-03-15T23:59:59.000Z

380

Phytoremediation of Metal-Contaminated Soils  

DOE Green Energy (OSTI)

Recent concerns regarding environmental contamination have necessitated the development of appropriate technologies to assess the presence and mobility of metals in soil and estimate possible ways to decrease the level of soil metal contamination. Phytoremediation is an emerging technology that may be used to cleanup contaminated soils. Successful application of phytoremediation, however, depends upon various factors that must be carefully investigated and properly considered for specific site conditions. To efficiently affect the metal removal from contaminated soils we used the ability of plants to accumulate different metals and agricultural practices to improve soil quality and enhance plant biomass. Pot experiments were conducted to study metal transport through bulk soil to the rhizosphere and stimulate transfer of the metals to be more available for plants' form. The aim of the experimental study was also to find fertilizers that could enhance uptake of metals and their removal from contaminated soil.

Shtangeeva, I.; Laiho, J.V-P.; Kahelin, H.; Gobran, G.R.

2004-03-31T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

Methods of selectively incorporating metals onto substrates  

DOE Patents (OSTI)

A method for forming multi-metallic sites on a substrate is disclosed and described. A substrate including active groups such as hydroxyl can be reacted with a pretarget metal complex. The target metal attached to the active group can then be reacted with a secondary metal complex such that an oxidation-reduction (redox) reaction occurs to form a multi-metallic species. The substrate can be a highly porous material such as aerogels, xerogels, zeolites, and similar materials. Additional metal complexes can be reacted to increase catalyst loading or control co-catalyst content. The resulting compounds can be oxidized to form oxides or reduced to form metals in the ground state which are suitable for practical use.

Ernst; Richard D. (Salt Lake City, UT), Eyring; Edward M. (Salt Lake City, UT), Turpin; Gregory C. (Salt Lake City, UT), Dunn; Brian C. (Salt Lake City, UT)

2008-09-30T23:59:59.000Z

382

Computation of methodology-independent single-ion solvation properties from molecular simulations. IV. Optimized Lennard-Jones interaction parameter sets for the alkali and halide ions in water  

Science Conference Proceedings (OSTI)

The raw single-ion solvation free energies computed from atomistic (explicit-solvent) simulations are extremely sensitive to the boundary conditions and treatment of electrostatic interactions used during these simulations. However, as shown recently [M. A. Kastenholz and P. H. Huenenberger, J. Chem. Phys. 124, 224501 (2006); M. M. Reif and P. H. Huenenberger, J. Chem. Phys. 134, 144103 (2010)], the application of appropriate correction terms permits to obtain methodology-independent results. The corrected values are then exclusively characteristic of the underlying molecular model including in particular the ion-solvent van der Waals interaction parameters, determining the effective ion size and the magnitude of its dispersion interactions. In the present study, the comparison of calculated (corrected) hydration free energies with experimental data (along with the consideration of ionic polarizabilities) is used to calibrate new sets of ion-solvent van der Waals (Lennard-Jones) interaction parameters for the alkali (Li{sup +}, Na{sup +}, K{sup +}, Rb{sup +}, Cs{sup +}) and halide (F{sup -}, Cl{sup -}, Br{sup -}, I{sup -}) ions along with either the SPC or the SPC/E water models. The experimental dataset is defined by conventional single-ion hydration free energies [Tissandier et al., J. Phys. Chem. A 102, 7787 (1998); Fawcett, J. Phys. Chem. B 103, 11181] along with three plausible choices for the (experimentally elusive) value of the absolute (intrinsic) hydration free energy of the proton, namely, {Delta}G{sub hyd} {sup O-minus} [H{sup +}]=-1100, -1075 or -1050 kJ mol{sup -1}, resulting in three sets L, M, and H for the SPC water model and three sets L{sub E}, M{sub E}, and H{sub E} for the SPC/E water model (alternative sets can easily be interpolated to intermediate {Delta}G{sub hyd} {sup O-minus} [H{sup +}] values). The residual sensitivity of the calculated (corrected) hydration free energies on the volume-pressure boundary conditions and on the effective ionic radius entering into the calculation of the correction terms is also evaluated and found to be very limited. Ultimately, it is expected that comparison with other experimental ionic properties (e.g., derivative single-ion solvation properties, as well as data concerning ionic crystals, melts, solutions at finite concentrations, or nonaqueous solutions) will permit to validate one specific set and thus, the associated {Delta}G{sub hyd} {sup O-minus} [H{sup +}] value (atomistic consistency assumption). Preliminary results (first-peak positions in the ion-water radial distribution functions, partial molar volumes of ionic salts in water, and structural properties of ionic crystals) support a value of {Delta}G{sub hyd} {sup O-minus} [H{sup +}] close to -1100 kJ{center_dot}mol{sup -1}.

Reif, Maria M.; Huenenberger, Philippe H. [Laboratory of Physical Chemistry, ETH Zuerich, CH-8093 Zuerich (Switzerland)

2011-04-14T23:59:59.000Z

383

Metals  

Science Conference Proceedings (OSTI)

Mar 2, 2011... and enthalpy change together with the off-gas composition recorded ... or stabilizing it first and then disposing of it in a specially-lined landfill.

384

Metals  

Science Conference Proceedings (OSTI)

Mar 13, 2012 ... Strong market demand for secondary materials has restricted material ... by chemical analysis using atomic absorption spectrophotometry in order to ... used for many applications such as secondary battery, cemented carbide,...

385

Metals  

Science Conference Proceedings (OSTI)

Feb 17, 2010... slags were analyzed by XRD and SEM-EDS, whilst their chemical stability was evaluated by leaching with an aqueous acetic acid solution.

386

Method and apparatus for dissociating metals from metal compounds extracted into supercritical fluids  

DOE Patents (OSTI)

A method for dissociating metal-ligand complexes in a supercritical fluid by treating the metal-ligand complex with heat and/or reducing or oxidizing agents is described. Once the metal-ligand complex is dissociated, the resulting metal and/or metal oxide form fine particles of substantially uniform size. In preferred embodiments, the solvent is supercritical carbon dioxide and the ligand is a .beta.-diketone such as hexafluoroacetylacetone or dibutyldiacetate. In other preferred embodiments, the metals in the metal-ligand complex are copper, silver, gold, tungsten, titanium, tantalum, tin, or mixtures thereof. In preferred embodiments, the reducing agent is hydrogen. The method provides an efficient process for dissociating metal-ligand complexes and produces easily-collected metal particles free from hydrocarbon solvent impurities. The ligand and the supercritical fluid can be regenerated to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Hunt, Fred H. (Moscow, ID); Smart, Neil G. (Workington, GB); Lin, Yuehe (Richland, WA)

2000-01-01T23:59:59.000Z

387

Data:Ad068fce-1967-4634-93f1-d6d742f406fa | Open Energy Information  

Open Energy Info (EERE)

Michigan (Utility Company) Effective date: 20120101 End date if known: Rate name: LED-100 Watt Metal Halide Equivalent: Dusk to Dawn Sector: Lighting Description: Rate D...

388

ComEd - Business Instant Lighting Discounts Program (Illinois...  

Open Energy Info (EERE)

Industrial, Multi-Family Residential, Private Schools Eligible Technologies Lighting, LED Lighting, Reduced Wattage Metal Halide Lamps, LED Trim Kits, Screw-In CFL's Active...

389

Data:4d20e878-ce9b-4cde-bd1a-50e7c4fb3b1c | Open Energy Information  

Open Energy Info (EERE)

Michigan (Utility Company) Effective date: 20120101 End date if known: Rate name: LED-100 Watt Metal Halide Equivalent (On Timer) Sector: Lighting Description: Rate D...

390

Weather durability testing and failures in terrestrial flat plate ...  

Science Conference Proceedings (OSTI)

... Atlas XR-260 large scale xenon weathering device ... & standard Atlas xenon Weather-Ometers) ... Atlas SolarClimatic 1600 metal-halide global solar ...

2013-11-15T23:59:59.000Z

391

NETL F 451.1-1/1 Categorical Exclusion (CX) Designation Form  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

NC Commercial Industrial and Large Profit- Gibralter Packaging Retrofitting and Re-commissioning Approximately 500 T12 and 250 metal halide lights and electronic ballasts will be...

392

Optical Indices of Refraction for Ce  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

393

Characterization of the Mechanical Properties of Two N-Type and ...  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

394

Nanostructured Electrodes for High-Performance Supercapacitors  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

395

Synthesis and Characterization of ?-Gallia-Rutile Intergrowth ...  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

396

The Absorption of Hydrogen on Low Pressure Hydride Materials  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

397

Electrochemical Charge/Discharge Behavior of Li-Mg Alloy Anodes ...  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

398

Smoothed Boundary Simulation of Electrochemical Processes in ...  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

399

Reliability Considerations for Second Life Applications for Used EV ...  

Science Conference Proceedings (OSTI)

Planar Sodium Metal Halide Battery for Renewable Integration and Grid ... Progress on Technology of Redox Flow Battery and Its Application in China.

400

Industry Group Learns About Light Source Opportunities  

NLE Websites -- All DOE Office Websites (Extended Search)

industry over the past 50 years. General Electric's "Durathon" sodium metal halide battery breakthrough required the use of light sources allowing them to understand the...

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Exhibit F-3  

U.S. Energy Information Administration (EIA) Indexed Site

on All Night Outdoor Lights with a Timer, Motion Sensor, or Photosensor Outdoor Gas Light High Intensity Discharge (HID) Outdoor Lights (Such as metal halide or high pressure...

402

Structural Formation and Oxidation Resistance of Si-Al-Y Co ...  

Science Conference Proceedings (OSTI)

Symposium, Advanced Protective Coatings for Refractory Metals and Alloys ... Halide activated pack cementation (HAPC) is an effective way to produce diffusive...

403

Appliances and Commercial Equipment Standards  

NLE Websites -- All DOE Office Websites (Extended Search)

certain lighting system components, but with only minor exceptions (torchieres, ceiling fan light kits, exit signs, traffic signals, and metal halide lamp fixtures), has not...

404

CX-006430: Categorical Exclusion Determination | Department of...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

high-pressure sodium, metal halide or mercury vapor lamps with energy efficient light emitting diode fixtures. DOCUMENT(S) AVAILABLE FOR DOWNLOAD CX-006430.pdf More Documents &...

405

CX-002106: Categorical Exclusion Determination | Department of...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

and Renewable Energy 1) Replacement of the metal-halide lighting with light-emitting diode energy efficient lighting in the two multi-floor buildings constituting the...

406

Data:26c74797-0d1d-4729-8521-708e6868be4d | Open Energy Information  

Open Energy Info (EERE)

known: Rate name: security light- 400 watt Metal Halide Sector: Lighting Description: * Energy usage 195 kWh. Subject to Power Cost Recovery Factor. Source or reference: http:...

407

Browse wiki | Open Energy Information  

Open Energy Info (EERE)

OpenEIUtilityRateDescription Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

408

Data:445d426e-8503-4331-82d7-db5b8d07dd8f | Open Energy Information  

Open Energy Info (EERE)

MV without Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

409

Data:65c9cfff-dc25-4b05-9ee9-d5d70bb2e905 | Open Energy Information  

Open Energy Info (EERE)

HPS without Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

410

Data:847d6419-dcc8-4499-bc82-52909c8067ca | Open Energy Information  

Open Energy Info (EERE)

HPS without Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

411

Data:4383f60e-b140-4087-b642-a716217c9927 | Open Energy Information  

Open Energy Info (EERE)

W MV with Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

412

Data:A36f0169-8028-4fc9-954c-071b63d0811c | Open Energy Information  

Open Energy Info (EERE)

W HPS with Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

413

Data:468fda37-fb88-408b-a804-bcdacd6f23aa | Open Energy Information  

Open Energy Info (EERE)

W HPS with Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

414

Data:3e340fd3-e49a-44bd-8c4a-16fa47debe51 | Open Energy Information  

Open Energy Info (EERE)

HPS without Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

415

Data:9f63edce-619a-4ae5-acbc-06d752f31d2d | Open Energy Information  

Open Energy Info (EERE)

HPS without Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

416

Data:A97d4360-0ad8-4d10-ad37-23a878a1e3f7 | Open Energy Information  

Open Energy Info (EERE)

MV without Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

417

Data:D02e240e-0b03-4a55-a0cb-2fb21d990680 | Open Energy Information  

Open Energy Info (EERE)

W HPS with Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

418

Data:4df36a5c-1301-4c53-9017-92328028cfe4 | Open Energy Information  

Open Energy Info (EERE)

MV without Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

419

Data:Bf2519c7-759c-4e83-80ef-406e0a5f00d9 | Open Energy Information  

Open Energy Info (EERE)

MHHPS 400 W) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

420

Data:820e509f-d2b1-4345-bf6d-240d05d98b17 | Open Energy Information  

Open Energy Info (EERE)

HPSMV with Pole) Sector: Lighting Description: Applicable only to outdoor lighting by ballast operated vapor lamp fixtures, either Mercury Vapor, Pressure Sodium, or Metal Halide....

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

About Fermilab - The Fermilab Campus  

NLE Websites -- All DOE Office Websites (Extended Search)

in the accelerator and some experimental beam lines and apparatus. Other energy-saving projects include: metal halide lighting to provide better illumination at lower cost...

422

Polymer quenched prealloyed metal powder  

DOE Patents (OSTI)

A powder metallurgical process of preparing a sheet from a powder having an intermetallic alloy composition such as an iron, nickel or titanium aluminide. The sheet can be manufactured into electrical resistance heating elements having improved room temperature ductility, electrical resistivity, cyclic fatigue resistance, high temperature oxidation resistance, low and high temperature strength, and/or resistance to high temperature sagging. The iron aluminide has an entirely ferritic microstructure which is free of austenite and can include, in weight %, 4 to 32% Al, and optional additions such as .ltoreq.1% Cr, .gtoreq.0.05% Zr .ltoreq.2% Ti, .ltoreq.2% Mo, .ltoreq.1% Ni, .ltoreq.0.75% C, .ltoreq.0.1% B, .ltoreq.1% submicron oxide particles and/or electrically insulating or electrically conductive covalent ceramic particles, .ltoreq.1% rare earth metal, and/or .ltoreq.3 % Cu. The process includes forming a non-densified metal sheet by consolidating a powder having an intermetallic alloy composition such as by roll compaction, tape casting or plasma spraying, forming a cold rolled sheet by cold rolling the non-densified metal sheet so as to increase the density and reduce the thickness thereof and annealing the cold rolled sheet. The powder can be a water, polymer or gas atomized powder which is subjecting to sieving and/or blending with a binder prior to the consolidation step. After the consolidation step, the sheet can be partially sintered. The cold rolling and/or annealing steps can be repeated to achieve the desired sheet thickness and properties. The annealing can be carried out in a vacuum furnace with a vacuum or inert atmosphere. During final annealing, the cold rolled sheet recrystallizes to an average grain size of about 10 to 30 .mu.m. Final stress relief annealing can be carried out in the B2 phase temperature range.

Hajaligol, Mohammad R. (Midlothian, VA); Fleischhauer, Grier (Midlothian, VA); German, Randall M. (State College, PA)

2001-01-01T23:59:59.000Z

423

Amorphous Metal Transformer: Next Steps  

Science Conference Proceedings (OSTI)

Amorphous-metal transformers were developed through EPRI in the early 1980's. Over the next 15 years, US electric utilities bought and installed over 500,000 units and had satisfactory field experience. The demand for this product disappeared in North America late in the 1990's as deregulation set-in. Globally, this product has been in use, and its acceptance has been increasing. This paper describes the current state of amorphous transformer activities globally. An analysis using US Department of Energy...

2009-07-31T23:59:59.000Z

424

Metal recovery from porous materials  

DOE Patents (OSTI)

A method for recovering plutonium and other metals from materials by leaching comprising the steps of incinerating the materials to form a porous matrix as the residue of incineration, immersing the matrix into acid in a microwave-transparent pressure vessel, sealing the pressure vessel, and applying microwaves so that the temperature and the pressure in the pressure vessel increase. The acid for recovering plutonium can be a mixture of HBF.sub.4 and HNO.sub.3 and preferably the pressure is increased to at least 100 PSI and the temperature to at least 200.degree. C. The porous material can be pulverized before immersion to further increase the leach rate.

Sturcken, Edward F. (P.O. Box 900, Isle of Palms, SC 29451)

1992-01-01T23:59:59.000Z

425

DISPERSION HARDENING OF URANIUM METAL  

DOE Patents (OSTI)

A method of hardening U metal involves the forming of a fine dispersion of UO/sub 2/. This method consists of first hydriding the U to form a finely divided powder and then exposing the powder to a very dilute O gas in an inert atmosphere under such pressure and temperature conditions as to cause a thin oxide film to coat each particle of the U hydride, The oxide skin prevents agglomeration of the particles as the remaining H is removed, thus preserving the small particle size. The oxide skin coatings remain as an oxide dispersion. The resulting product may be workhardened to improve its physical characteristics. (AEC)

Arbiter, W.

1963-01-15T23:59:59.000Z

426

An Ultracapacitor - Battery Energy Storage System for Hybrid Electric Vehicles.  

E-Print Network (OSTI)

??The nickel metal hydride (NiMH) batteries used in most hybrid electric vehicles (HEVs) provide satisfactory performance but are quite expensive. In spite of their lower (more)

Stienecker, Adam W

2005-01-01T23:59:59.000Z

427

table of contents  

Science Conference Proceedings (OSTI)

Hydrometallurgical Treatment of Nickel-Metal Hydride Battery Electrodes J.W. Lyman ... Recycling Process of Used Ni-MH Rechargeable Batteries T. Yoshida...

428

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (Los Alamos, NM); Delhaize, Emmanuel (Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-01-01T23:59:59.000Z

429

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat unit for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heayv metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (both Los Alamos, NM); Delhaize, Emmanuel (both Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-11-13T23:59:59.000Z

430

Nanostructured metal foams: synthesis and applications  

DOE Green Energy (OSTI)

Fabrication of monolithic metallic nanoporous materials is difficult using conventional methodology. Here they report a relatively simple method of synthesizing monolithic, ultralow density, nanostructured metal foams utilizing self-propagating combustion synthesis of novel metal complexes containing high nitrogen energetic ligands. Nanostructured metal foams are formed in a post flame-front dynamic assembly with densities as low as 0.011 g/cc and surface areas as high as 270 m{sup 2}/g. They have produced metal foams via this method of titanium, iron, cobalt, nickel, zirconium, copper, palladium, silver, hafnium, platinum and gold. Microstructural features vary as a function of composition and process parameters. Applications for the metal foams are discussed including hydrogen absorption in palladium foams. A model for the sorption kinetics of hydrogen in the foams is presented.

Luther, Erik P [Los Alamos National Laboratory; Tappan, Bryce [Los Alamos National Laboratory; Mueller, Alex [Los Alamos National Laboratory; Mihaila, Bogdan [Los Alamos National Laboratory; Volz, Heather [Los Alamos National Laboratory; Cardenas, Andreas [Los Alamos National Laboratory; Papin, Pallas [Los Alamos National Laboratory; Veauthier, Jackie [Los Alamos National Laboratory; Stan, Marius [Los Alamos National Laboratory

2009-01-01T23:59:59.000Z

431

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly ({gamma}-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly ({gamma}-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, P.J.; Delhaize, E.; Robinson, N.J.; Unkefer, C.J.; Furlong, C.

1988-08-26T23:59:59.000Z

432

Coupling apparatus for a metal vapor laser  

DOE Patents (OSTI)

Coupling apparatus for a large bore metal vapor laser is disclosed. The coupling apparatus provides for coupling high voltage pulses (approximately 40 KV) to a metal vapor laser with a high repetition rate (approximately 5 KHz). The coupling apparatus utilizes existing thyratron circuits and provides suitable power input to a large bore metal vapor laser while maintaining satisfactory operating lifetimes for the existing thyratron circuits.

Ball, D.G.; Miller, J.L.

1993-02-23T23:59:59.000Z

433

Liquid metal cooled nuclear reactor plant system  

DOE Patents (OSTI)

A liquid metal cooled nuclear reactor having a passive cooling system for removing residual heat resulting for fuel decay during reactor shutdown, or heat produced during a mishap. The reactor system is enhanced with sealing means for excluding external air from contact with the liquid metal coolant leaking from the reactor vessel during an accident. The invention also includes a silo structure which resists attack by leaking liquid metal coolant, and an added unique cooling means.

Hunsbedt, Anstein (Los Gatos, CA); Boardman, Charles E. (Saratoga, CA)

1993-01-01T23:59:59.000Z

434

Method for making monolithic metal oxide aerogels  

DOE Patents (OSTI)

Transparent, monolithic metal oxide aerogels of varying densities are produced using a method in which a metal alkoxide solution and a catalyst solution are prepared separately and reacted. The resulting hydrolyzed-condensed colloidal solution is gelled, and the wet gel is contained within a sealed, but gas permeable, containment vessel during supercritical extraction of the solvent. The present invention is especially advantageous for making metal oxides other than silica that are prone to forming opaque, cracked aerogels.

Droege, Michael W. (Livermore, CA); Coronado, Paul R. (Livermore, CA); Hair, Lucy M. (Livermore, CA)

1995-01-01T23:59:59.000Z

435

Method for making monolithic metal oxide aerogels  

DOE Patents (OSTI)

Transparent, monolithic metal oxide aerogels of varying densities are produced using a method in which a metal alkoxide solution and a catalyst solution are prepared separately and reacted. The resulting hydrolyzed-condensed colloidal solution is gelled, and the wet gel is contained within a sealed, but gas permeable, containment vessel during supercritical extraction of the solvent. The containment vessel is enclosed within an aqueous atmosphere that is above the supercritical temperature and pressure of the solvent of the metal alkoxide solution.

Coronado, Paul R. (Livermore, CA)

1999-01-01T23:59:59.000Z

436

Method for making monolithic metal oxide aerogels  

DOE Patents (OSTI)

Transparent, monolithic metal oxide aerogels of varying densities are produced using a method in which a metal alkoxide solution and a catalyst solution are prepared separately and reacted. The resulting hydrolyzed-condensed colloidal solution is gelled, and the wet gel is contained within a sealed, but gas permeable, containment vessel during supercritical extraction of the solvent. The present invention is especially advantageous for making metal oxides other than silica that are prone to forming opaque, cracked aerogels. 6 figs.

Droege, M.W.; Coronado, P.R.; Hair, L.M.

1995-03-07T23:59:59.000Z

437

Metal oxide composite dosimeter method and material  

DOE Patents (OSTI)

The present invention is a method of measuring a radiation dose wherein a radiation responsive material consisting essentially of metal oxide is first exposed to ionizing radiation. The metal oxide is then stimulating with light thereby causing the radiation responsive material to photoluminesce. Photons emitted from the metal oxide as a result of photoluminescence may be counted to provide a measure of the ionizing radiation.

Miller, Steven D. (Richland, WA)

1998-01-01T23:59:59.000Z

438

Method of stripping metals from organic solvents  

DOE Patents (OSTI)

A new method to strip metals from organic solvents in a manner that allows for the recycle of the stripping agent. The method utilizes carbonate solutions of organic amines with complexants, in low concentrations, to strip metals from organic solvents. The method allows for the distillation and reuse of organic amines. The concentrated metal/complexant fraction from distillation is more amenable to immobilization than solutions resulting from current practice.

Todd, Terry A. (Aberdeen, ID); Law, Jack D. (Pocatello, ID); Herbst, R. Scott (Idaho Falls, ID); Romanovskiy, Valeriy N. (St. Petersburg, RU); Smirnov, Igor V. (St.-Petersburg, RU); Babain, Vasily A. (St-Petersburg, RU); Esimantovski, Vyatcheslav M. (St-Petersburg, RU)

2009-02-24T23:59:59.000Z

439

Improvements in fabrication of metallic fuels  

Science Conference Proceedings (OSTI)

Argonne National Laboratory is currently developing a new liquid- metal cooled breeder reactor known as the Integral Fast Reactor (IFR). IFR fuels represent the state-of-the-art in metal-fueled reactor technology. Improvements in the fabrication of metal fuel, to be discussed below, will support the fully remote fuel cycle facility that as an integral part of the IFR concept will be demonstrated at the EBR-II site. 3 refs.

Tracy, D.B.; Henslee, S.P.; Dodds, N.E.; Longua, K.J.

1989-12-01T23:59:59.000Z

440

Synthesis of new amorphous metallic spin glasses  

DOE Patents (OSTI)

Amorphous metallic precipitates having the formula (M.sub.1).sub.a (M.sub.2).sub.b wherein M.sub.1 is at least one transition metal, M.sub.2 is at least one main group metal and the integers "a" and "b" provide stoichiometric balance; the precipitates having a degree of local order characteristic of chemical compounds from the precipitation process and useful electrical and mechanical properties.

Haushalter, Robert C. (Clinton, NJ)

1986-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

Synthesis of new amorphous metallic spin glasses  

DOE Patents (OSTI)

Disclosed are: amorphous metallic precipitates having the formula (M/sub 1/)/sub a/(M/sub 2/)/sub b/ wherein M/sub 1/ is at least one transition metal, M/sub 2/ is at least one main group metal and the integers ''a'' and ''b'' provide stoichiometric balance; the precipitates having a degree of local order characteristic of chemical compounds from the precipitation process and useful electrical and mechanical properties.

Haushalter, R.C.

1985-02-11T23:59:59.000Z

442

Synthesis of new amorphous metallic spin glasses  

DOE Patents (OSTI)

Amorphous metallic precipitates having the formula (M.sub.1).sub.a (M.sub.2).sub.b wherein M.sub.1 is at least one transition metal, M.sub.2 is at least one main group metal and the integers "a" and "b" provide stoichiometric balance; the precipitates having a degree of local order characteristic of chemical compounds from the precipitation process and useful electrical and mechanical properties.

Haushalter, Robert C. (Clinton, NJ)

1988-01-01T23:59:59.000Z

443

Understanding the Dynamic Indentation Behaviour of Metallic ...  

Science Conference Proceedings (OSTI)

In contrast, the dynamic indentation hardness behaviour of metallic materials, characterized by ultra-high strain rate plastic deformation under adiabatic...

444

Dealloyed Nanoporous Metals for Energy Storage  

Science Conference Proceedings (OSTI)

Dealloyed Nanoporous Metals for Energy Storage Design of Light Weight Structure for Wind Turbine Tower by Using Nano-Materials Development of Highly...

445

Separation of metal ions from aqueous solutions  

DOE Patents (OSTI)

This invention is comprised of a process and apparatus for quantitatively and selectively separating metal ions from mixtures thereof in aqueous solution. The apparatus includes, in combination, a horizontal electrochemical flowing cell containing flowing bulk electrolyte solution and an aqueous, metal ion-containing solution, the cell containing a metal mesh working electrode, a counter electrode positioned downstream from the working electrode, an independent variable power supply/potentiostat positioned outside of the flowing cell and connected to the electrodes, and optionally a detector such as a chromatographic detector, positioned outside the flowing cell. This apparatus and its operation has significant application where trace amounts of metal ions are to be separated.

Almon, A.

1991-12-31T23:59:59.000Z

446

PRODUCTION OF URANIUM METAL BY CARBON REDUCTION  

DOE Patents (OSTI)

The preparation of uranium metal by the carbon reduction of an oxide of uranium is described. In a preferred embodiment of the invention a charge composed of carbon and uranium oxide is heated to a solid mass after which it is further heated under vacuum to a temperature of about 2000 deg C to produce a fused uranium metal. Slowly ccoling the fused mass produces a dendritic structure of uranium carbide in uranium metal. Reacting the solidified charge with deionized water hydrolyzes the uranium carbide to finely divide uranium dioxide which can be separated from the coarser uranium metal by ordinary filtration methods.

Holden, R.B.; Powers, R.M.; Blaber, O.J.

1959-09-22T23:59:59.000Z

447

THE COORDINATION CHEMISTRY OF METAL SURFACES  

E-Print Network (OSTI)

48 and the cluster chemistry by the The nickel and platinumL. Muetterties Department of Chemistry, Lawrence Berkeleyphenomenon in metal surface chemistry. Ultra high vacuw:n

Muetterties, Earl L.

2013-01-01T23:59:59.000Z

448

Non-Noble Metal Water Electrolysis Catalysts  

This invention comprises an inexpensive catalyst system for water electrolyzers by replacing the noble-metal catalysts that are typically used in ...

449

Smaller is Stronger in Amorphous Metals  

Science Conference Proceedings (OSTI)

Author(s), Chengcai Wang, Zhiwei Shan, Jun Sun, Ju Li, Evan Ma. On-Site Speaker (Planned) .... Metallic Glasses for Electro-Catalytic Applications Micro- Scale...

450

Smithells Metals Reference Book (8th Edition)  

Science Conference Proceedings (OSTI)

Feb 12, 2007 ... This comprehensive reference provides data on all key aspects of metallic materials, including narrative information on metallurgical and...

451

Specific complexation of metal oxo cations  

DOE Patents (OSTI)

The present invention relates to novel chelating agents for high molecular weight polyvalent metal oxo cations. Specifically, an improved chelating agent and an improved process of chelation is described to recognize specifically metal oxo cations using organic chelating agents that have a functional group to supply donor groups for metal coordination while simultaneously providing a different group to intramolecularly interact with the oxygen of the oxo group. More precisely, the invention relates to tripodal amine carboxylates useful to sequester uranyl and related metal oxo cations in aqueous solution, and is especially suitable for recovering such oxo cations from dilute aqueous solutions, e.g. seawater, mine runoff, processing waste streams, etc.

Raymond, K.N.; Franczyk, T.S.

1990-12-17T23:59:59.000Z

452

Fourth International Symposium on Recycling of Metals  

Science Conference Proceedings (OSTI)

Combining Lead-Zinc 2000 and Recycling of Metals and Engineered ... Andreas Sigmund, RSR Technologies, Inc. Secondary Copper, Nickel and Cobalt

453

Fundamentals in Laser Additive Manufacturing of Metals  

Science Conference Proceedings (OSTI)

Presentation Title, Fundamentals in Laser Additive Manufacturing of Metals. Author(s), Xinjin Cao, Yinan Zhang, Priti Wanjara, Mamoun Medraj. On-Site Speaker...

454

Nanotube Reinforced Metal Matrix Composites II  

Science Conference Proceedings (OSTI)

Symposium, Nanotube Reinforced Metal Matrix Composites II. Sponsorship, MS&T Organization. Organizer(s), Indrajit Charit, University of Idaho Sudipta Seal ...

455

Treatment of Light Metal Wastes - TMS  

Science Conference Proceedings (OSTI)

... for the Treatment and Minimization of Wastes: Treatment of Light Metal Wastes ... A Decade of Gestation: S. Street, G. Brooks and H.K. Worner, Materials Eng.

456

"Radiative Liquid Lithium (metal) Divertor" Inventor..-- Masayuki...  

NLE Websites -- All DOE Office Websites (Extended Search)

"Radiative Liquid Lithium (metal) Divertor" Inventor..-- Masayuki Ono The invention utilizes liquid lithium as a radiative material. The radiative process greatly reduces the...

457

Partnering Today: Technology Transfer Highlights Metal ...  

The compressive stress signi?cantly increases the metal parts resistance to cracking or corrosion. By extending fatigue lifetimes, laser

458

Hutchison Effect Metal Samples: Description and Analysis  

Science Conference Proceedings (OSTI)

... and other equipment which caused severe plastic deformation, delamination, de-alloying and unusual magnetic properties in metal (aluminum, copper, brass,

459

Light-metal Matrix (Nano)-composites  

Science Conference Proceedings (OSTI)

There is a regaining interest in these metal-matrix composites, amongst others triggered by the use of nano-particle additions (oxides, carbides, nitrides,)...

460

Metal Current Collector Protected by Oxide Film  

For Industry; For Researchers; Success Stories; About Us; ... metal felt made substantially of inexpensive ferritic steel coated with a thin oxide film, ...

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

Gas Adsorption and Permeance with Metal Organic ...  

Science Conference Proceedings (OSTI)

... Page 4. ? Metal Organic Frameworks (MOFs) ? Zeolitic Imidazolate ... 1 2 2,1 P P = ? nRT A nRT PV = ? = ? 7 coupled equations, 9 unknowns ...

2010-09-03T23:59:59.000Z

462

Californium--palladium metal neutron source material  

DOE Patents (OSTI)

Californium, as metal or oxide, is uniformly dispersed throughout a noble metal matrix, provided in compact, rod or wire form. A solution of californium values is added to palladium metal powder, dried, blended and pressed into a compact having a uni-form distribution of californium. The californium values are decomposed to californium oxide or metal by heating in an inert or reducing atmosphere. Sintering the compact to a high density closes the matrix around the dispersed californium. The sintered compact is then mechanically shaped into an elongated rod or wire form. (4 claims, no drawings) (Official Gazette)

Dahlen, B.L.; Mosly, W.C. Jr.; Smith, P.K.; Albenesius, E.L.

1974-01-22T23:59:59.000Z

463

Metal Organic Frameworks for Clean Energy Applications  

Science Conference Proceedings (OSTI)

Symposium, Materials Issues in Nuclear Waste Management in the 21st Century. Presentation Title, Metal Organic Frameworks for Clean Energy Applications.

464

Plastic Deformation and Creep of Microcellular Metals  

Science Conference Proceedings (OSTI)

K. K. Chawla's Seminal Contributions to the Field of Metal Matrix Composites Structural Health Monitoring of Wind Turbine Blades Studies of Nanocrystalline ...

465

Mechanical Properties of Thin Film Metallic Glass  

Science Conference Proceedings (OSTI)

Because of these and other properties, thin film metallic-glasses (TFMGs) are a promising structural material for fabricating the next generation of micro- and...

466

Raman spectroscopy of metallic carbon nanotubes  

E-Print Network (OSTI)

Metallic carbon nanotubes are one dimensional conductors that are both technologically promising for electronic applications, and scientifically interesting for studying the physics of low dimensional materials. In this ...

Farhat, Hootan

2010-01-01T23:59:59.000Z

467

Evaluation of monolayer protected metal nanoparticle technology  

E-Print Network (OSTI)

Self assembling nanostructured nanoparticles represent a new class of synthesized materials with unique functionality. Such monolayer protected metal nanoparticles are capable of resisting protein adsorption, and if utilized ...

Wu, Diana J

2005-01-01T23:59:59.000Z

468

Mixed metal ?lms with switchable optical properties  

The electrochemical hydro-gen loading behavior of these mixed metal ?lms was similar ... Energy Ef?ciency and Renewable Energy, Of?ce of Building

469

Bioreductive recovery of platinum group metals by the metal-ion ...  

Science Conference Proceedings (OSTI)

The metal ion-reducing bacterium, Shewanella algae, was found to exhibit the ability to reduce and deposit the PGM ions (Pd(II), Pt(IV), Rh(III)) into metal...

470

Metallic Ferroelectricity and Superconductivity in the Transition Metal Oxide Pyrochlore Cd2Re2O7.  

E-Print Network (OSTI)

??Single crystalline samples of transition metal oxide Cd2Re2O7, the first superconductor among pyrochlore oxides with general formula A2B2O7 and the first example of ferroelectric metal (more)

He, Jian

2004-01-01T23:59:59.000Z

471

Numerical models for scoring failures of flexible metal to metal face seals  

E-Print Network (OSTI)

The flexible metal to metal face seals (FMMFS) has unique features including much more flexibility in the circumferential direction than in the radial direction, identical rotating and stationary seals, and a loading ...

Hong, Jinchul, 1977-

2005-01-01T23:59:59.000Z

472

Displacement method and apparatus for reducing passivated metal powders and metal oxides  

DOE Patents (OSTI)

A method of reducing target metal oxides and passivated metals to their metallic state. A reduction reaction is used, often combined with a flux agent to enhance separation of the reaction products. Thermal energy in the form of conventional furnace, infrared, or microwave heating may be applied in combination with the reduction reaction.

Morrell; Jonathan S. (Knoxville, TN), Ripley; Edward B. (Knoxville, TN)

2009-05-05T23:59:59.000Z

473

REDUCTION OF FLUORIDE TO METAL  

DOE Patents (OSTI)

A process is given for making yttrium metal by reducing yttrium fluoride with calcium plus magnesium. Calcium is added in an excess of from 10 to 20% and magnesium in a quantity to yield a magnesium--yttrium alloy containing from 12 to 25% magnesium when the reaction mass is heated in an inert atmosphere at from 900 to 1106 deg C, but preferably above the melting point of the alloy. Calcium chloride may be added so as to obtain a less viscous slag containing from 30 to 60% calcium chloride. After removal of the slag the alloy is vacuum-heated at about 1100 deg C for volatilization of the magnesium and calcium.

Carlson, O.N.; Schmidt, F.A.; Spedding, F.H.

1960-08-30T23:59:59.000Z

474

Metal recovery from porous materials  

DOE Patents (OSTI)

A method is described for recovering plutonium and other metals from materials by leaching comprising the steps of incinerating the materials to form a porous matrix as the residue of incineration, immersing the matrix into acid in a microwave-transparent pressure vessel, sealing the pressure vessel, and applying microwaves so that the temperature and the pressure in the pressure vessel increase. The acid for recovering plutonium can be a mixture of HBF[sub 4] and HNO[sub 3] and preferably the pressure is increased to at least 100 PSI and the temperature to at least 200 C. The porous material can be pulverized before immersion to further increase the leach rate.

Sturcken, E.F.

1992-10-13T23:59:59.000Z

475

Theoretical model of liquid metals  

Science Conference Proceedings (OSTI)

A theory for calculating the bulk properties of metals and other materials is described. The approach is based upon the fluid perturbation theory of Kerley and the electronic structure model of Liberman. Application of the theory involves three steps. First, the zero Kelvin isotherm of the solid is constructed from electronic structure calculations, experimental data, or both. This curve contains information about the effective interactions between atoms in the ground electronic state. Next, the cold curve is combined with perturbation theory to compute contributions from thermal motion of the atoms to the liquid properties. Finally, contributions from thermal electron excitation are computed using the electronic structure model. This paper shows that theory agrees well with experimental data for xenon and iron.

Kerley, G.I.

1981-01-01T23:59:59.000Z

476

BOF steelmaking without hot metal  

SciTech Connect

This paper will discuss implementation of Z-BOP technology at Iscor's New Castle plant. The implementation program and operating results of Z-BOP-100 technology will be covered. The unique experience of the BOF shop operation without hot metal supply from the blast furnaces will also be described. This experience was a result of proprietary Z-BOP technology implementation at Iscor during its sole blast furnace reline. The Z-BOP is a family of technologies operating with scrap ratios in the charge from 30 to 100%. These technologies can be used in conventional top-blown BOF with virtually no equipment modifications. The principal additional energy source is lump coal, fed through existing BOF bin systems. Different modification of Z-BOP, originally used on the industrial scale at the West Siberian Steel Works, Russia, were utilized at several BOF facilities worldwide. Performance of the process and its main characteristics are discussed.

Gitman, G.; Galperine, G.; Grenader, I. (Zap Tech. Corp., Norcross, GA (United States)); Van der Merwe, F.O.; Newton, R.L. (Iscor Ltd., New Castle (South Africa))

1993-07-01T23:59:59.000Z

477

Load relaxation studies of a metallic glass  

SciTech Connect

Experimental results of load relaxation studies of a commercial metallic glass as a function of temperature are reported. The data suggest that metallic glasses exhibit deformation behavior with flow laws similar to those governing plastic deformation in crystalline solids. The lack of appreciable work hardening in annealed material and the identification of an anelastic component are also indicated by the experimental observations. (GHT)

Hadnagy, T.D.; Krenisky, D.J.; Ast, D.G.; Li, C.Y.

1977-01-01T23:59:59.000Z

478

Heavy metals hazardous components of Eaf dust  

Science Conference Proceedings (OSTI)

Electric arc furnace (EAF) dust is a waste generated in the EAF during the steel production process. Among different wastes, EAF dust represents one of the most hazardous, since it contains heavy metals such as Zn, Fe, Cr, Cd and Pb. The goal of the ... Keywords: electric arc furnace (EAF), furnace additives, hazard components, heavy metals, scrap composition, x-ray fluorescence spectroscopy

Cristiana-Zizi Rizescu; Zorica Bacinschi; Elena Valentina Stoian; Aurora Poinescu; Dan Nicolae Ungureanu

2011-02-01T23:59:59.000Z

479

Heavy metals in suspended powders from steelmaking  

Science Conference Proceedings (OSTI)

Motivations for controlling heavy metal concentrations in gas streams are diverse. Some of them are dangerous to health or to the environment (e.g. Hg, Cd, As, Pb, Cr), some may cause corrosion (e.g. Zn, Pb), some are harmful in other ways (e.g. Arsenic ... Keywords: anthropogenic sources, emissions, heavy metals, human health, pollution of ecosystem, toxic

Cristiana-Zizi Rizescu; Elena-Valentina Stoian; Aurora-Anca Poinescu; Sofia Teodorescu

2010-07-01T23:59:59.000Z

480

APPARATUS FOR VACUUM DEPOSITION OF METALS  

DOE Patents (OSTI)

An apparatus and a method are described for continuous vacuum deposition of metals for metallic coatings, for ultra-high vacuum work, for purification of metals, for maintaining high-density electron currents, and for other uses. The apparatus comprises an externally cooled feeder tube extending into a container and adapted to feed metal wire or strip so that it emerges in a generally vertical position therein. The tube also provides shielding from the heat produced by an electron beam therein focused to impinge from a vertical direction upon the tip of the emerging wire. By proper control of the wire feed, coolant feed, and electron beam intensity, a molten ball of metal forms upon the emerging tip and remains self-supported thereon by the interaction of various forces. The metal is vaporized and travels in a line of sight direction, while additional wire is fed from the tube, so that the size of the molten ball remains constant. In the preferred embodiments, the wire is selected from a number of gettering metals and is degassed by electrical resistance in an adjacent chamber which is also partially evacuated. The wire is then fed through the feed tube into the electron beam and vaporizes and adsorbs gases to provide pumping action while being continuously deposited upon surfaces within the chamber. Ion pump electrodes may also be provided within line of sight of the vaporizing metal source to enhance the pumping action. (AEC)

Milleron, N.

1962-03-13T23:59:59.000Z

Note: This page contains sample records for the topic "metal halide mh" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


481

Process for electrolytically preparing uranium metal  

DOE Patents (OSTI)

A process for making uranium metal from uranium oxide by first fluorinating uranium oxide to form uranium tetrafluoride and next electrolytically reducing the uranium tetrafluoride with a carbon anode to form uranium metal and CF.sub.4. The CF.sub.4 is reused in the fluorination reaction rather than being disposed of as a hazardous waste.

Haas, Paul A. (Knoxville, TN)

1989-01-01T23:59:59.000Z

482

Metallic nanoshells on porphyrin-stabilized emulsions  

SciTech Connect

Metal nanostructures formed by photocatalytic interfacial synthesis using a porphyrin-stabilized emulsion template and the method for making the nanostructures. Catalyst-seeded emulsion droplets are employed as templates for hollow-nanoshell growth. The hollow metal nanospheres may be formed with or without inclusions of other materials.

Wang, Haorong; Song, Yujiang; Shelnutt, John A; Medforth, Craig J

2013-10-29T23:59:59.000Z

483

Process for making silver metal filaments  

DOE Patents (OSTI)

This invention relates to a process for making filaments of metal compounds and more particularly to a process for making silver metal filaments. The United States Government has rights to this invention pursuant to Contract No. DE-AC05-8421400 with Lockheed Martin Energy Systems, Inc. awarded by the US Department of Energy.

Bamberger, C.E.

1998-04-01T23:59:59.000Z

484

High temperature ceramic/metal joint structure  

DOE Patents (OSTI)

A high temperature turbine engine includes a hybrid ceramic/metallic rotor member having ceramic/metal joint structure. The disclosed joint is able to endure higher temperatures than previously possible, and aids in controlling heat transfer in the rotor member.

Boyd, Gary L. (Tempe, AZ)

1991-01-01T23:59:59.000Z

485

Process for the disposal of alkali metals  

SciTech Connect

Large quantities of alkali metals may be safely reacted for ultimate disposal by contact with a hot concentrated caustic solution. The alkali metals react with water in the caustic solution in a controlled reaction while steam dilutes the hydrogen formed by the reaction to a safe level.

Lewis, Leroy C. (Arco, ID)

1977-01-01T23:59:59.000Z

486

Nanocomposite of graphene and metal oxide materials  

SciTech Connect

Nanocomposite materials comprising a metal oxide bonded to at least one graphene material. The nanocomposite materials exhibit a specific capacity of at least twice that of the metal oxide material without the graphene at a charge/discharge rate greater than about 10C.

Liu, Jun; Aksay, Ilhan A.; Choi, Daiwon; Wang, Donghai; Yang, Zhenguo

2012-09-04T23:59:59.000Z

487

City of Frankfort, Kentucky (Utility Company) | Open Energy Information  

Open Energy Info (EERE)

Frankfort City of Frankfort City of Place Kentucky Utility Id 6708 Utility Location Yes Ownership M NERC Location RFC NERC RFC Yes Activity Transmission Yes Activity Distribution Yes Activity Bundled Services Yes References EIA Form EIA-861 Final Data File for 2010 - File1_a[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Utility Rate Schedules Grid-background.png Area Lighting- (1000W MH With 35' Metal Pole) Lighting Area Lighting- (1000W MH With 35' Wood Pole) Lighting Area Lighting- (1000W MH With 45' Metal Pole) Lighting Area Lighting- (250W MH With 35' Metal Pole) Lighting Area Lighting- (250W MH With 35' Wood Pole) Lighting Area Lighting- (320W MH With 35' Metal Pole) Lighting

488

Visualizing Brain Metals in Health and Disease  

NLE Websites -- All DOE Office Websites (Extended Search)

Visualizing Brain Metals in Health and Visualizing Brain Metals in Health and Disease figure 1 Fig. 1. Rapid-scanning x-ray fluorescence mapping ex perimental setup. Synchrotron x-rays at 11 keV passed through a 50 µm aperture (Ap). The beam intensity was monitored with a N2-filled ion chamber (I0). The brain slice was mounted vertically on a motorized stage (St) at 45° to the incident x-ray beam and raster scanned in the beam. A 13-element Ge detector (Ge) was positioned at a 90° angle to the beam. We all require iron, copper and zinc for normal brain function but metal metabolism becomes dysregulated in a variety of neurodegenerative diseases. Metals accumulate in Alzheimer's dementia and Parkinson's disease and are deficient in Menkes disease. Whether excess metals appear as a cause or a

489

Rare Earth Metals and Alloys | Ames Laboratory  

NLE Websites -- All DOE Office Websites (Extended Search)

Mpc » Rare Earth Metals and Alloys Mpc » Rare Earth Metals and Alloys Rare Earth Metals and Alloys Terbium (Tb) and Cerium (Ce) phosphors in your computer screen allow you to see GREEN. Europium (Eu) is the source of the RED light and BLUE emitted by our display. The Ames Laboratory has been actively involved in the preparation of very pure rare earth metals since the early 1940's when Dr. Frank H. Spedding and his group of pioneers developed the ion-exchange process, a technique that separates the "fraternal fifteen" plus yttrium and scandium. As a result of this and subsequent work, high-purity oxides are available from which high-purity rare earth metals can be prepared. In most cases, the rare earth oxides are first converted to their respective fluorides and are then reduced metallothermicaly on a kilogram

490

Lithium metal oxide electrodes for lithium batteries  

DOE Patents (OSTI)

An uncycled electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula Li.sub.(2+2x)/(2+x)M'.sub.2x/(2+x)M.sub.(2-2x)/(2+x)O.sub.2-.delta., in which 0.ltoreq.x<1 and .delta. is less than 0.2, and in which M is a non-lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. Methods of preconditioning the electrodes are disclosed as are electrochemical cells and batteries containing the electrodes.

Thackeray, Michael M. (Naperville, IL); Kim, Jeom-Soo (Naperville, IL); Johnson, Christopher S. (Naperville, IL)

2008-01-01T23:59:59.000Z

491

Dinuclear Metalloradicals Featuring Unsupported Metal-Metal Bonds  

Science Conference Proceedings (OSTI)

Unlike the very labile, unobservable radical cations [{l_brace}CpM(CO){sub 3}{r_brace}{sub 2}]{sup {sm_bullet}+} (M = W, Mo), derivatives [{l_brace}CpM(CO){sub 2}(PMe{sub 3}){r_brace}{sub 2}]{sup {sm_bullet}+} are stable enough to be isolated and characterized. Experimental and theoretical studies show that the shortened M-M bonds are of order 1 1/2, and that they are not supported by bridging ligands. The unpaired electron is fully delocalized, with a spin density of ca. 45% on each metal atom. We thank the U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Biosciences and Geosciences for support of this work. Pacific Northwest National Laboratory (PNNL) is a multiprogram national laboratory operated for DOE by Battelle. The EPR and computational studies were performed using EMSL, a national scientific user facility sponsored by the DOE's Office of Biological and Environmental Research and located at PNNL. We thank Dr. Charles Windisch for access to his UV-Vis-NIR spectrometer.

van der Eide, Edwin F.; Yang, Ping; Walter, Eric D.; Liu, Tianbiao L.; Bullock, R. Morris

2012-08-13T23:59:59.000Z

492

Thermodynamics and kinetics of ceramic/metal interfacial interactions  

E-Print Network (OSTI)

Ceramic/metal interfaces occur in a great number of important applications, such as ceramic/metal composites, microelectronics packaging, ceramic/metal seals, and so forth. Understanding the formation and evolution of such ...

Arryave, Raymundo, 1975-

2004-01-01T23:59:59.000Z

493

Metallic diffusion process and improved article produced thereby  

DOE Patents (OSTI)

A uniquely surface-modified metallic part is provided by the utilization of microwave energy to promote diffusion of desired metals into the surface of the formed metallic part.

Morrow, M. Stanley (Kingston, TN); Schechter, Donald E. (Ten Mile, TN); Grant, Harley A. (Harrison, TN)

2003-04-29T23:59:59.000Z

494

Audit of the Department of Energy's Management of Precious Metals...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Precious Metals, IG-0375 Audit of the Department of Energy's Management of Precious Metals, IG-0375 Audit of the Department of Energy's Management of Precious Metals, IG-0375 More...

495

Development of Bulk Metallic Glasses with High Plasticity Using the ...  

Science Conference Proceedings (OSTI)

Air-Oxidation of a (Zr55Cu30Al10Ni5)98Er2 Bulk Metallic Glass at 350-500oc Anelastic Deformation of a Metallic Glass Anisotropy in Metallic Glasses.

496

Spectroscopic studies of metal growth on oxides  

E-Print Network (OSTI)

Metal/oxide chemistry and metal cluster growth on oxides are fundamental to our understanding of the catalytic activity and selectivity of metal catalysts, thus considerable research recently has addressed the physical and chemical properties of metal clusters on well-defined oxide surfaces. In this work, the nucleation and growth modes of Ag on TiO?(110)(1x1) and (1x2) surfaces, Ag on ultra-thin Al?O? films, and Au on ultra-thin SiO? films were studied by scanning tunneling microscopy (STM), low energy ion scattering spectroscopy (LEIS) and X-ray photoelectron spectroscopy (XPS). In general, Ag grows three-dimensionally (3D) on both TiO?(110) and Al?O? film at 300 K. The growth mode of Au at fractional monolayer coverages is quasi-two dimensional (2D); at higher coverages, three-dimensional growth of Au was found. In these three systems, Ag/TiO?, Ag/Al?O?, and Au/SiO?, no strong chemical interaction was observed between metal clusters and substrates. Sintering was observed for all metal clusters upon annealing. A non-zero order desorption was observed for Ag/Al?O? and Au/SiO? in temperature programmed desorption (TPD) studies. The desorption activation energies decrease with decreasing metal coverages.

Luo, Kai

2000-01-01T23:59:59.000Z

497

Zone refining of plutonium metal  

Science Conference Proceedings (OSTI)

The purpose of this study was to investigate zone refining techniques for the purification of plutonium metal. The redistribution of 10 impurity elements from zone melting was examined. Four tantalum boats were loaded with plutonium impurity alloy, placed in a vacuum furnace, heated to 700{degrees}C, and held at temperature for one hour. Ten passes were made with each boat. Metallographic and chemical analyses performed on the plutonium rods showed that, after 10 passes, moderate movement of certain elements were achieved. Molten zone speeds of 1 or 2 inches per hour had no effect on impurity element movement. Likewise, the application of constant or variable power had no effect on impurity movement. The study implies that development of a zone refining process to purify plutonium is feasible. Development of a process will be hampered by two factors: (1) the effect on impurity element redistribution of the oxide layer formed on the exposed surface of the material is not understood, and (2) the tantalum container material is not inert in the presence of plutonium. Cold boat studies are planned, with higher temperature and vacuum levels, to determine the effect on these factors. 5 refs., 1 tab., 5 figs.

NONE

1997-05-01T23:59:59.000Z

498

Electrodynamic separation of metallic granules from mixed waste stream.  

E-Print Network (OSTI)

??Metals are essential, reusable resources. The reusable nature of metal contributes to the sustainability of its use through recycling, which will reduce landfill disposal and (more)

Naidu, Harini

2010-01-01T23:59:59.000Z

499

WEB RESOURCE: Direct Metal Laser Sintering (DMLS) Brochure  

Science Conference Proceedings (OSTI)

Dec 11, 2007 ... This brochure describes the Direct Metal Laser Sinterning (DMLS) process to make end-use metal parts directly from 3D CAD data.

500

Characterization of Non Ferrous Metals - Programmaster.org  

Science Conference Proceedings (OSTI)

... in the search for improved metallic alloys for various plasmonic applications. ... Al to monovalent noble metal Ag on the shifting of the interband transitions to...