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Note: This page contains sample records for the topic "acids alkalies salts" from the National Library of EnergyBeta (NLEBeta).
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1

Salt Fluxes for Alkali and Alkaline Earth Element Removal from ...  

Science Conference Proceedings (OSTI)

Sep 1, 2001... for Alkali and Alkaline Earth Element Removal from Molten Aluminum ... Solid chloride salts containing MgC2 can be used to remove alkali ...

2

Salts of alkali metal anions and process of preparing same  

DOE Patents (OSTI)

Compounds of alkali metal anion salts of alkali metal cations in bicyclic polyoxadiamines are disclosed. The salts are prepared by contacting an excess of alkali metal with an alkali metal dissolving solution consisting of a bicyclic polyoxadiamine in a suitable solvent, and recovered by precipitation. The salts have a gold-color crystalline appearance and are stable in a vacuum at -10.degree. C. and below.

Dye, James L. (East Lansing, MI); Ceraso, Joseph M. (Lansing, MI); Tehan, Frederick J. (Utica, NY); Lok, Mei Tak (Urbana, IL)

1978-01-01T23:59:59.000Z

3

Oxygen production by molten alkali metal salts using multiple absorption-desorption cycles  

DOE Patents (OSTI)

A continuous chemical air separation is performed wherein oxygen is recovered with a molten alkali metal salt oxygen acceptor in a series of absorption zones which are connected to a plurality of desorption zones operated in separate parallel cycles with the absorption zones. A greater recovery of high pressure oxygen is achieved at reduced power requirements and capital costs.

Cassano, Anthony A. (Allentown, PA)

1985-01-01T23:59:59.000Z

4

Oxygen production by molten alkali metal salts using multiple absorption-desorption cycles  

DOE Patents (OSTI)

A continuous chemical air separation is performed wherein oxygen is recovered with a molten alkali metal salt oxygen acceptor in a series of absorption zones which are connected to a plurality of desorption zones operated in separate parallel cycles with the absorption zones. A greater recovery of high pressure oxygen is achieved at reduced power requirements and capital costs. 3 figs.

Cassano, A.A.

1985-07-02T23:59:59.000Z

5

Synthesis of an acid addition salt of delta-aminolevulinic acid from 5-bromo levulinic acid esters  

DOE Patents (OSTI)

A process is disclosed for preparing an acid addition salt of delta-aminolevulinic acid comprising. The process involves dissolving a lower alkyl 5-bromolevulinate and an alkali metal diformylamide in an organic solvent selected from the group consisting of acetonitrile, methanol, tetrahydrofuran, 2-methyltetrahydrofuran and methylformate or mixtures to form a suspension of an alkyl 5-(N,N-diformylamino) levulinate ester; and hydrolyzing the alkyl 5-(N,N-diformylamino) levulinate with an inorganic acid to form an acid addition salt of delta-amino levulinic acid.

Moens, L.

1999-05-25T23:59:59.000Z

6

Synthesis of acid addition salt of delta-aminolevulinic acid ...  

A process of preparing an acid addition salt of delta-aminolevulinc acid comprising: a) dissolving a lower alkyl 5-bromolevulinate and hexamethylenetetramine in a ...

7

Process for the preparation of 3,4-dihydroxybutanoic acid and salts thereof  

DOE Patents (OSTI)

A process for the preparation of 3,4-dihydroxybutanoic acid (1) and salts thereof from a glucose source containing 1,4-linked glucose as a substituent is described. The process uses an alkali metal hdyroxide and hydrogen peroxide to convert the glucose source to (1). The compound (1) is useful as a chemical intermediate to naturally occurring fatty acids and is used to prepare 3,4-dihydroxybutanoic acid-gamma-lactone (2) and furanone (3), particularly stereoisomers of these compounds.

Hollingsworth, Rawle I. (Haslett, MI)

1994-01-01T23:59:59.000Z

8

Process For The Preparation Of 3,4-Dihyd Roxybutanoic Acid And Salts Thereof  

DOE Patents (OSTI)

A process for the preparation of 3,4-dihydroxybutanoic acid (1) and salts thereof from a glucose source containing 1,4-linked glucose as a substituent is described. The process uses an alkali metal hdyroxide and hydrogen peroxide to convert the glucose source to (1). The compound (1) is useful as a chemical intermediate to naturally occurring fatty acids and is used to prepare 3,4-dihydroxybutanoic acid-gamma-lactone (2) and furanone (3), particularly stereoisomers of these compounds.

Hollingsworth, Rawle I. (Haslett, MI)

1994-06-07T23:59:59.000Z

9

Methanol synthesis using a catalyst combination of alkali or alkaline earth salts and reduced copper chromite  

DOE Patents (OSTI)

The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a catalyst combination comprising reduced copper chromite and basic alkali salts or alkaline earth salts. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100--160 C and the pressure range of 40--65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H[sub 2]/CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

Tierney, J.W.; Wender, I.; Palekar, V.M.

1995-01-24T23:59:59.000Z

10

Methanol synthesis using a catalyst combination of alkali or alkaline earth salts and reduced copper chromite  

DOE Patents (OSTI)

The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a catalyst combination comprising reduced copper chromite and basic alkali salts or alkaline earth salts. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100.degree.-160.degree. C. and the pressure range of 40-65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H.sub.2 /CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

Tierney, John W. (Pittsburgh, PA); Wender, Irving (Pittsburgh, PA); Palekar, Vishwesh M. (Pittsburgh, PA)

1995-01-01T23:59:59.000Z

11

Alkali Treatment of Acidic Solution from Hanford K Basin Sludge Dissolution  

SciTech Connect

Nitric acid solutions will be created from the dissolution of Hanford K Basin sludge. These acidic dissolver solutions must be made alkaline by treatment with NaOH solution before they are disposed to ~ the Tank Waste Remediation System on the Hanford Site. During the alkali treatments, sodium diuranate, hydroxides of iron and aluminum, and radioelements (uranium, plutonium, and americium) will precipitate from the dissolver solution. Laboratory tests, discussed here, were pefiormed to provide information on these precipitates and their precipitation behavior that is important in designing the engineering flowsheet for the treatment process. Specifically, experiments were conducted to determine the optimum precipitation conditions; the completeness of uranium, plutonium, and americium precipitation; the rate of sedimentation; and the physico-chemical characteristics of the solids formed by alkali treatment of simulated acidic dissolver solutions. These experiments also determined the redistribution of uranium, plutonium, and americium flom the sodium di~ate and iron and al&inurn hydroxide precipitates upon contact with carbonate- and EDTA-bearing simulated waste solutions. Note: EDTA is the tetrasodium salt of ethylenediaminetetraacetate.

AA Bessonov; AB Yusov; AM Fedoseev; AV Gelis; AY Garnov; CH Delegard; GM Plavnik; LN Astafurova; MS Grigoriev; NA Budantseva; NN Krot; SI Nikitenko; TP Puraeva; VP Perminov; VP Shilov

1998-12-22T23:59:59.000Z

12

Synthesis of acid addition salt of delta-aminolevulinic acid from 5-bromo levulinic acid esters  

DOE Patents (OSTI)

A process of preparing an acid addition salt of delta-aminolevulinc acid comprising: a) dissolving a lower alkyl 5-bromolevulinate and hexamethylenetetramine in a solvent selected from the group consisting of water, ethyl acetate, chloroform, acetone, ethanol, tetrahydrofuran and acetonitrile, to form a quaternary ammonium salt of the lower alkyl 5-bromolevulinate; and b) hydrolyzing the quaternary ammonium salt with an inorganic acid to form an acid addition salt of delta-aminolevulinic acid.

Moens, Luc (Lakewood, CO)

2003-06-24T23:59:59.000Z

13

Process for the preparation of 3,4-dihydroxybutanoic acid and salts thereof  

DOE Patents (OSTI)

A process for the preparation of 3,4-dihydroxybutanoic acid (1) and salts thereof from a glucose source containing 1,4-1inked glucose as a substituent is described. The process uses an alkali metal hdyroxide and hydrogen peroxide to convert the glucose source to (1). The compound (1) is useful as a chemical intermediate to naturally occurring fatty acids and is used to prepare 3,4-dihydroxybutanoic acid-gamma-lactone (2) and furanone (3), particularly stereoisomers of these compounds.

Hollingsworth, Rawle I. (Haslett, MI)

1994-01-01T23:59:59.000Z

14

Metal salts of alkyl catechol dithiophosphoric acids and oil compositions containing the salts  

Science Conference Proceedings (OSTI)

Metal salts of alkyl catechol esters of dithiophosphoric acid suitable as additives in oil compositions are disclosed in this patent. Oil compositions containing the salts of such esters show improved extreme pressure/anti-wear and anit-oxidant properties.

Yamaguchi, E.S.; Liston, T.V.

1988-03-08T23:59:59.000Z

15

In situ formation of coal gasification catalysts from low cost alkali metal salts  

DOE Patents (OSTI)

A carbonaceous material, such as crushed coal, is admixed or impregnated with an inexpensive alkali metal compound, such as sodium chloride, and then pretreated with a stream containing steam at a temperature of 350.degree. to 650.degree. C. to enhance the catalytic activity of the mixture in a subsequent gasification of the mixture. The treatment may result in the transformation of the alkali metal compound into another, more catalytically active, form.

Wood, Bernard J. (Santa Clara, CA); Brittain, Robert D. (Cupertino, CA); Sancier, Kenneth M. (Menlo Park, CA)

1985-01-01T23:59:59.000Z

16

Methanol synthesis using a catalyst combination of alkali or alkaline earth salts and reduced copper chromite for methanol synthesis  

DOE Patents (OSTI)

The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a catalyst combination comprising reduced copper chromite and basic alkali salts or alkaline earth salts. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100.degree.-160.degree. C. and the pressure range of 40-65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H.sub.2 /CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

Tierney, John W. (Pittsburgh, PA); Wender, Irving (Pittsburgh, PA); Palekar, Vishwesh M. (Pittsburgh, PA)

1993-01-01T23:59:59.000Z

17

Production of chlorine from chloride salts  

DOE Patents (OSTI)

A process for converting chloride salts and sulfuric acid to sulfate salts and elemental chlorine is disclosed. A chloride salt and sulfuric acid are combined in a furnace where they react to produce a sulfate salt and hydrogen chloride. Hydrogen chloride from the furnace contacts a molten salt mixture containing an oxygen compound of vanadium, an alkali metal sulfate and an alkali metal pyrosulfate to recover elemental chlorine. In the absence of an oxygen-bearing gas during the contacting, the vanadium is reduced, but is regenerated to its active higher valence state by separately contacting the molten salt mixture with an oxygen-bearing gas.

Rohrmann, Charles A. (Kennewick, WA)

1981-01-01T23:59:59.000Z

18

Plutonium and americium separation from salts  

DOE Patents (OSTI)

Salts or materials containing plutonium and americium are dissolved in hydrochloric acid, heated, and contacted with an alkali metal carbonate solution to precipitate plutonium and americium carbonates which are thereafter readily separable from the solution.

Hagan, Paul G. (Northglenn, CO); Miner, Frend J. (Boulder, CO)

1976-01-01T23:59:59.000Z

19

Method and system for producing lower alcohols. [Heteropolyatomic lead salt coated with alkali metal formate  

DOE Patents (OSTI)

It is an object of the present invention to provide an improved catalyst for the reaction of carbon monoxide with water to produce methanol and other lower alcohols. It is a further object to provide a process for the production of methanol from carbon monoxide and water in which a relatively inexpensive catalyst permits the reaction at low pressures. It is also an object to provide a process for the production of methanol from carbon monoxide and water in which a relatively inexpensive catalyst permits the reaction at low pressures. It is also an object to provide a process for the production of methanol in which ethanol is also directly produced. It is another object to provide a process for the production of mixtures of methanol with ethanol and propanol from the reaction of carbon monoxide and water at moderate pressure with inexpensive catalysts. It is likewise an object to provide a system for the catalytic production of lower alcohols from the reaction of carbon monoxide and water at moderate pressure with inexpensive catalysts. In accordance with the present invention, a catalyst is provided for the reaction of carbon monoxide and water to produce lower alcohols. The catalyst includes a lead heteropolyatomic salt in mixture with a metal formate or a precursor to a metal formate.

Rathke, J.W.; Klingler, R.J.; Heiberger, J.J.

1983-09-26T23:59:59.000Z

20

Conversion of carboxylate salts to carboxylic acids via reactive distillation  

E-Print Network (OSTI)

The purpose of this study is to convert carboxylate salts (e.g. calcium acetate, propionate, and butyrate) into carboxylic acids (e.g., acetic, propionic, and butyric acids). The carboxylate salts can be produced from wastes, such as paper fines, municipal solid wastes, sewage sludge, and industrial biosludge. Using a proprietary technology owned by Texas A&M University the wastes are first treated with lime to enhance reactivity. Then they are converted to calcium carboxylate salts using a mixed culture of microorganisms derived from cattle rumen or anaerobic waste treatment facilities. The paper fines and municipal solid waste provide energy, whereas the industrial biosludge and sewage sludge provide nutrients for the microorganisms. The calcium carboxylate salts are concentrated and reacted with a low-molecular-weight tertiary amine and carbon dioxide to precipitate calcium carbonate. In a distillation column, the low-molecular-weight amine carboxylate reacts with a high-molecular-weight tertiary amine allowing the low-molecular-weight amine to be recovered from the top of the column. The resulting high-molecular-weight amine carboxylate is converted to amine and carboxylic acid in a reactive distillation column. This project focuses on the conversion of the carboxylate salts produced via fermentation into their corresponding acids via reactive distillation. The primary objective is to determine the optimal operating conditions of the distillation. A secondary objective is to optimize the precipitation step in the recovery process.

Williamson, Shelly Ann

2000-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Dilute acid/metal salt hydrolysis of lignocellulosics  

DOE Patents (OSTI)

A modified dilute acid method of hydrolyzing the cellulose and hemicellulose in lignocellulosic material under conditions to obtain higher overall fermentable sugar yields than is obtainable using dilute acid alone, comprising: impregnating a lignocellulosic feedstock with a mixture of an amount of aqueous solution of a dilute acid catalyst and a metal salt catalyst sufficient to provide higher overall fermentable sugar yields than is obtainable when hydrolyzing with dilute acid alone; loading the impregnated lignocellulosic feedstock into a reactor and heating for a sufficient period of time to hydrolyze substantially all of the hemicellulose and greater than 45% of the cellulose to water soluble sugars; and recovering the water soluble sugars.

Nguyen, Quang A. (Golden, CO); Tucker, Melvin P. (Lakewood, CO)

2002-01-01T23:59:59.000Z

22

Electrolytic method to make alkali alcoholates using ion conducting alkali electrolyte/separator  

DOE Patents (OSTI)

Alkali alcoholates, also called alkali alkoxides, are produced from alkali metal salt solutions and alcohol using a three-compartment electrolytic cell. The electrolytic cell includes an anolyte compartment configured with an anode, a buffer compartment, and a catholyte compartment configured with a cathode. An alkali ion conducting solid electrolyte configured to selectively transport alkali ions is positioned between the anolyte compartment and the buffer compartment. An alkali ion permeable separator is positioned between the buffer compartment and the catholyte compartment. The catholyte solution may include an alkali alcoholate and alcohol. The anolyte solution may include at least one alkali salt. The buffer compartment solution may include a soluble alkali salt and an alkali alcoholate in alcohol.

Joshi, Ashok V. (Salt Lake City, UT); Balagopal, Shekar (Sandy, UT); Pendelton, Justin (Salt Lake City, UT)

2011-12-13T23:59:59.000Z

23

Catalyst of a metal heteropoly acid salt that is insoluble in ...  

Catalyst of a metal heteropoly acid salt that is insoluble in a polar solvent on a non-metallic porous support and method of making United States Patent

24

Salt  

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

Salt Salt Nature Bulletin No. 340-A April 12, 1969 Forest Preserve District of Cook County George W. Dunne, President Roland F. Eisenbeis, Supt. of Conservation SALT It is fortunate that Salt -- common salt, known to chemists as sodium chloride and to mineralogists as Halite -- is one of the most abundant substances on earth, because most of us crave it and must have it. Eskimos get along without salt because they live mostly on the uncooked flesh of fish and mammals. A few nomad tribes never eat it and do not need it because their diet contains so much milk cheese, and meat eaten raw or roasted. We people who eat boiled meat and many vegetables must have salt. Of the millions of tons produced commercially each year, only about three percent is used as table salt. Large quantities are required for refrigeration meat packing, curing and preserving fish, pickles, sauerkraut, and for other foods prepared in brine. A lot of it is needed for livestock. Salt is spread on sidewalks, streets and highways to melt ice in winter. It is used to glaze pottery, sewer pipe and other ceramics. It is required in many metallurgical processes, chemical industries, and the manufacture of such products as leather, glass, soap, bleaching powder and photographic supplies. It has about 14,000 uses.

25

Ion Partitioning at the liquid/vapor interface of a multi-component alkali halide solution: A model for aqueous sea salt aerosols  

E-Print Network (OSTI)

model for aqueous sea salt aerosols Sutapa Ghosal, 1 Matthewwith sea salt ice and aerosols has been implicated in theof aqueous sea salt aerosols and particles have been

Ghosal, Sutapa

2009-01-01T23:59:59.000Z

26

Nitric Acid–Sea Salt Reactions: Implications for Nitrogen Deposition to Water Surfaces  

Science Conference Proceedings (OSTI)

Many previous studies have indicated the importance of nitric acid (HNO3) reactions on sea salt particles for flux divergence of HNO3 in the marine surface layer. The potential importance of this reaction in determining the spatial and temporal ...

S. C. Pryor; L. L. Sørensen

2000-05-01T23:59:59.000Z

27

Studies on the production of ultra-clean coal by alkali-acid leaching of low-grade coals  

Science Conference Proceedings (OSTI)

The use of low-grade coal in thermal power stations is leading to environmental pollution due to the generation of large amounts of fly ash, bottom ash, and CO{sub 2} besides other pollutants. It is therefore important to clean the coal before using it in thermal power stations, steel plants, or cement industries etc. Physical beneficiation of coal results in only limited cleaning of coal. The increasing environmental pollution problems from the use of coal have led to the development of clean coal technologies. In fact, the clean use of coal requires the cleaning of coal to ultra low ash contents, keeping environmental norms and problems in view and the ever-growing need to increase the efficiency of coal-based power generation. Therefore this requires the adaptation of chemical cleaning techniques for cleaning the coal to obtain ultra clean coal having ultra low ash contents. Presently the reaction conditions for chemical demineralization of low-grade coal using 20% aq NaOH treatment followed by 10% H{sub 2}SO{sub 4} leaching under reflux conditions have been optimized. In order to reduce the concentration of alkali and acid used in this process of chemical demineralization of low-grade coals, stepwise, i.e., three step process of chemical demineralization of coal using 1% or 5% aq NaOH treatment followed by 1% or 5% H{sub 2}SO{sub 4} leaching has been developed, which has shown good results in demineralization of low-grade coals. In order to conserve energy, the alkali-acid leaching of coal was also carried out at room temperature, which gave good results.

Nabeel, A.; Khan, T.A.; Sharma, D.K. [Jamia Millia Islamia, New Delhi (India). Dept. of Chemistry

2009-07-01T23:59:59.000Z

28

Tropospheric Chemistry of Internally Mixed Sea Salt and Organic Particles: Surprising Reactivity of NaCl with Weak Organic Acids  

Science Conference Proceedings (OSTI)

Chemical imaging analysis of internally mixed sea salt/organic particles collected on board the Department of Energy (DOE) G-1 aircraft during the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES) was performed using electron microscopy and X-ray spectro-microscopy techniques. Substantial chloride depletion in aged sea salt particles was observed, which could not be explained by the known atmospheric reactivity of sea salt with inorganic nitric and sulfuric acids. We present field evidence that chloride components in sea salt particles may effectively react with organic acids releasing HCl gas to the atmosphere, leaving behind particles depleted in chloride and enriched in the corresponding organic salts. While formation of the organic salts products is not thermodynamically favored for bulk aqueous chemistry, these reactions in aerosol are driven by high volatility and irreversible evaporation of the HCl product from drying particles. These field observations were corroborated in a set of laboratory experiments where NaCl particles mixed with organic acids were found to be depleted in chloride. Combined together, the results indicate substantial chemical reactivity of sea salt particles with secondary organics that has been largely overlooked in the atmospheric aerosol chemistry. Atmospheric aging, and especially hydration-dehydration cycles of mixed sea salt/organic particles may result in formation of organic salts that will modify acidity, hygroscopic and optical properties of aged particles.

Laskin, Alexander; Moffet, Ryan C.; Gilles, Marry K.; Fast, Jerome D.; Zaveri, Rahul A.; Wang, Bingbing; Nigge, P.; Shutthanandan, Janani I.

2012-08-03T23:59:59.000Z

29

Method for the safe disposal of alkali metal  

DOE Patents (OSTI)

Alkali metals such as those employed in liquid metal coolant systems can be safely reacted to form hydroxides by first dissolving the alkali metal in relatively inert metals such as lead or bismuth. The alloy thus formed is contacted with a molten salt including the alkali metal hydroxide and possibly the alkali metal carbonate in the presence of oxygen. This oxidizes the alkali metal to an oxide which is soluble within the molten salt. The salt is separated and contacted with steam or steam-CO.sub.2 mixture to convert the alkali metal oxide to the hydroxide. These reactions can be conducted with minimal hydrogen evolution and with the heat of reaction distributed between the several reaction steps.

Johnson, Terry R. (Wheaton, IL)

1977-01-01T23:59:59.000Z

30

Enhancement of specific heat capacity of high-temperature silica-nanofluids synthesized in alkali chloride salt eutectics for solar thermal-energy  

E-Print Network (OSTI)

chloride salt eutectics for solar thermal-energy storage applications Donghyun Shin, Debjyoti Banerjee solution, resulting in degradation of the thermal properties. Solar energy conversion to electricity is achieved primarily by using (a) photovoltaic technology, or (b) by harnessing solar thermal-energy

Banerjee, Debjyoti

31

Concentrating aqueous volatile fatty acid salt solutions using a tertiary amine mixture  

E-Print Network (OSTI)

Lee (1993) has shown that tertiary amines are able to hics. extract water from low-concentration calcium acetate and sodium acetate solutions. This thesis extends the previous work to include calcium propionate and butyrate. Amine extraction may be used to selectively remove water from a fermentation broth thus concentrating calcium acetate, propionate, and butyrate. Compared to competing technologies that extract undissociated acids from a volatile fatty acid fermentation broth, extracting water with tertiary amines allows for higher pH levels in the broth resulting in greater productivity. Specifically, triethylamine and N,N-diethyl-methylamine in a 1:2 volumetric mixture are superior to any other examined mixture or single amine for extracting water at 40[]C, the proposed fermentation temperature (Lee, 1993; Davison et al., 1966, 1967). Once the acid salts have been concentrated, a variety of techniques are available to convert the concentrated salts into other products such as ketones, alcohols, and acids. At low temperatures, the low-molecular-weight amine mixture has a high affinity for water. By raising the temperature 20 to 25[]C, the water separates from the amine allowing for convenient solvent regeneration of the amine. The distribution coefficients, [] , measure the selectivity of concentrating calcium salts in the aqueous phase. The distribution coefficients generally vary as follows: [] thus, there is less selectivity as the aliphatic group increases in size. The amine mixture was used to extract water from actual fermentation broth to determine whether possible surfactants in the broth interfere with the extraction. Prior to extraction, the fermentation broth was adjusted to pH 11.5 by adding a small amount of lime. The high pH precipitate protein which can be recycled to the fermentor or collected for animal feed. Through 15 extraction runs, no degradation of the amine was observed.

Gaskin, David J

1997-01-01T23:59:59.000Z

32

Method for intercalating alkali metal ions into carbon electrodes  

DOE Patents (OSTI)

A low cost, relatively flexible, carbon electrode for use in a secondary battery is described. A method is provided for producing same, including intercalating alkali metal salts such as sodium and lithium into carbon.

Doeff, M.M.; Ma, Y.; Visco, S.J.; DeJonghe, L.

1995-08-22T23:59:59.000Z

33

Method for intercalating alkali metal ions into carbon electrodes  

SciTech Connect

A low cost, relatively flexible, carbon electrode for use in a secondary battery is described. A method is provided for producing same, including intercalating alkali metal salts such as sodium and lithium into carbon.

Doeff, Marca M. (Hayward, CA); Ma, Yanping (Berkeley, CA); Visco, Steven J. (Berkeley, CA); DeJonghe, Lutgard (Lafayette, CA)

1995-01-01T23:59:59.000Z

34

Extraction of metals and/or metalloids from acidic media using supercritical fluids and salts  

DOE Patents (OSTI)

A method is described for extracting metalloid and metal species from a solid or liquid material by exposing the material to a fluid solvent, particularly supercritical carbon dioxide, containing a chelating agent. The chelating agent forms chelates that are soluble in the fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent comprises a trialkyl phosphate, a triaryl phosphate, a trialkylphosphine oxide, a triarylphosphine oxide, or mixtures thereof. The method provides an environmentally benign process for removing contaminants from industrial waste. The method is particularly useful for extracting actinides from acidic solutions, and the process can be aided by the addition of nitrate salts. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process. 7 figs.

Wai, C.M.; Smart, N.G.; Lin, Y.

1998-06-23T23:59:59.000Z

35

Extraction of metals and/or metalloids from acidic media using supercritical fluids and salts  

DOE Patents (OSTI)

A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a fluid solvent, particularly supercritical carbon dioxide, containing a chelating agent is described. The chelating agent forms chelates that are soluble in the fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent comprises a trialkyl phosphate, a triaryl phosphate, a trialkylphosphine oxide, a triarylphosphine oxide, or mixtures thereof. The method provides an environmentally benign process for removing contaminants from industrial waste. The method is particularly useful for extracting actinides from acidic solutions, and the process can be aided by the addition of nitrate salts. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Smart, Neil G. (Moscow, ID); Lin, Yuehe (Moscow, ID)

1998-01-01T23:59:59.000Z

36

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

37

Characterization of Selective Binding of Alkali Cations with Carboxylate  

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

Characterization of Selective Characterization of Selective Binding of Alkali Cations with Carboxylate Characterization of Selective Binding of Alkali Cations with Carboxylate Print Wednesday, 24 September 2008 00:00 During its lifetime, a cell spends a considerable fraction of its energy pumping sodium and calcium out and potassium in. This balancing process is similar to that found in the coils of the DNA double helix, where specific ions nestle and help stabilize this macromolecule. These are only two examples of selective ion interactions in biology; there are many others also vital to life. The existence of these interactions has been known since the early 20th century, when Franz Hofmeister observed that some salts (ionic compounds) aided the solution of proteins in egg, some caused proteins to destabilize and precipitate, and others ranged in activity between the two extremes. Hofmeister then ranked "salt-out" (destabilizing) ions versus "salt-in" (stabilizing) ions according to the magnitude of their effects (the "Hofmeister effects"). However, despite enormous effort, why certain interactions are preferred over others is not completely understood. Recently, a team of researchers from UC Berkeley used the model systems of acetate and formate (two simple carboxylic acids) with a series of cations to test predictions made in the literature for preferential interactions. Near-edge x-ray absorption fine structure (NEXAFS) spectroscopy was used as this technique is highly sensitive to the chemical environments around a molecule. Experiments at ALS Beamline 8.0.1 confirmed strengthening of the interaction between the cations and the carboxylate group in the following order: potassium, sodium, and lithium.

38

Impact of Alkali Source on Vitrification of SRS High Level Waste  

SciTech Connect

The Defense Waste Processing Facility (DWPF) Savannah River Site is currently immobilizing high level nuclear waste sludge by vitrification in borosilicate glass. The processing strategy involves blending a large batch of sludge into a feed tank, washing the sludge to reduce the amount of soluble species, then processing the large ''sludge batch'' through the DWPF. Each sludge batch is tested by the Savannah River National Laboratory (SRNL) using simulants and tests with samples of the radioactive waste to ''qualify'' the batch prior to processing in the DWPF. The DWPF pretreats the sludge by first acidifying the sludge with nitric and formic acid. The ratio of nitric to formic acid is adjusted as required to target a final glass composition that is slightly reducing (the target is for {approx}20% of the iron to have a valence of two in the glass). The formic acid reduces the mercury in the feed to elemental mercury which is steam stripped from the feed. After a concentration step, the glass former (glass frit) is added as a 50 wt% slurry and the batch is concentrated to approximately 50 wt% solids. The feed slurry is then fed to a joule heated melter maintained at 1150 C. The glass must meet both processing (e.g., viscosity and liquidus temperature) and product performance (e.g., durability) constraints The alkali content of the final waste glass is a critical parameter that affects key glass properties (such as durability) as well as the processing characteristics of the waste sludge during the pretreatment and vitrification processes. Increasing the alkali content of the glass has been shown to improve the production rate of the DWPF, but the total alkali in the final glass is limited by constraints on glass durability and viscosity. Two sources of alkali contribute to the final alkali content of the glass: sodium salts in the waste supernate and sodium and lithium oxides in the glass frit added during pretreatment processes. Sodium salts in the waste supernate can be reduced significantly by washing the solids to remove soluble species. The ''washing strategy'' for future sludge batches can be controlled to limit the soluble sodium remaining in the waste stream while balancing the alkali content of the frit to maintain acceptable glass properties as well as improve melter processing characteristics.

LAMBERT, D. P.; MILLER, D. H.; PEELER, D. K.; SMITH, M. E.; STONE, M. E.

2005-09-08T23:59:59.000Z

39

A Chemical Study of Oils and Fats of Animal OriginChapter 2 Chevreul-discovered Fatty Acids and their Salts  

Science Conference Proceedings (OSTI)

A Chemical Study of Oils and Fats of Animal Origin Chapter 2 Chevreul-discovered Fatty Acids and their Salts Food Science eChapters Food Science & Technology Press Downloadable pdf of Chapter 2 Chevreul-discovered

40

Primary cell of high energy density in which the anode active material is an alkali metal  

Science Conference Proceedings (OSTI)

A primary cell of high specific energy in which the anode active material is an alkali metal and the cathode active material is sulphur oxychloride which simultaneously acts as an electrolyte solvent, said electrolyte further containing a dissolved salt and a co-solvent. The co-solvent is chosen from among phosphoryl chloride and benzoyl chloride; the dissolved salt is lithium tetrachloroaluminate.

Gabano, J.

1983-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

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

42

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

43

Molten salt thermal energy storage systems: salt selection  

DOE Green Energy (OSTI)

A research program aimed at the development of a molten salt thermal energy storage system commenced in June 1976. This topical report describes Work performed under Task I: Salt Selection is described. A total of 31 inorganic salts and salt mixtures, including 9 alkali and alkaline earth carbonate mixtures, were evaluated for their suitability as heat-of-fusion thermal energy storage materials at temperatures of 850 to 1000/sup 0/F. Thermophysical properties, safety hazards, corrosion, and cost of these salts were compared on a common basis. We concluded that because alkali carbonate mixtures show high thermal conductivity, low volumetric expansion on melting, low corrosivity and good stability, they are attractive as heat-of-fusion storage materials in this temperature range. A 35 wt percent Li/sub 2/CO/sub 3/-65 wt percent K/sub 2/CO/sub 3/ (50 mole percent Li/sub 2/CO/sub 3/-50 mole percent K/sub 2/CO/sub 3/) mixture was selected as a model system for further experimental work. This is a eutectoid mixture having a heat of fusion of 148 Btu/lb (82 cal/g) that forms an equimolar compound, LiKCO/sub 3/. The Li/sub 2/CO/sub 3/-K/sub 2/CO/sub 3/ mixture is intended to serve as a model system to define heat transfer characteristics, potential problems, and to provide ''first-cut'' engineering data required for the prototype system. The cost of a thermal energy storage system containing this mixture cannot be predicted until system characteristics are better defined. However, our comparison of different salts indicated that alkali and alkaline earth chlorides may be more attractive from a salt cost point of view. The long-term corrosion characteristics and the effects of volume change on melting for the chlorides should be investigated to determine their overall suitability as a heat-of-fusion storage medium.

Maru, H.C.; Dullea, J.F.; Huang, V.S.

1976-08-01T23:59:59.000Z

44

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

45

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

46

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

47

Evaluation of Alkali Bromide Salts for Potential Pyrochemical Applications  

SciTech Connect

Transient techniques were employed to study the electrochemical behavior, reduction mechanism and transport properties of REBr3 (RE - La, Nd and Gd) in pure LiBr, LiBr-KBr (eutectic) and LiBr-KBr-CsBr (eutectic) melts. Gd(III) showed a reversible single step soluble-insoluble exchange phenomenon in LiBr melt at 973K. Although La (III), Nd(III) and Gd(III) ions showed reversible behavior in eutectic LiBr-KBr melts, these ions showed a combination of temperature dependent reversible and pseudo-reversible behavior. While both La(III) and Gd(III) showed one step reduction, the reduction of Nd(III) was observed to be a two step process. La metal could be electrodeposited from the ternary electrolyte at a temperature of 673K. Various electrochemical measurements suggest that both binary and ternary bromide melts can potentially be used to electrodeposit high purity RE metals at comparatively lower operating temperatures.

Prabhat K. Tripathy; Steven D. Herrmann; Guy L. Fredrickson; Tedd E. Lister; Toni Y. Gutknecht

2013-10-01T23:59:59.000Z

48

Alkali Resistant Refractories - Oak Ridge National Laboratory  

Alkali Resistant Refractories Note: The technology described above is an early stage opportunity. Licensing rights to this intellectual property may

49

Tungsten-188/carrier-free rhenium-188 perrhenic acid generator system  

DOE Patents (OSTI)

A generator system for providing a carrier-free radioisotope in the form of an acid comprises a chromatography column in tandem fluid connection with an ion exchange column, the chromatography column containing a charge of a radioactive parent isotope. The chromatography column, charged with a parent isotope, is eluted with an alkali metal salt solution to generate the radioisotope in the form of an intermediate solution, which is passed through the ion-exchange column to convert the radioisotope to a carrier-free acid form.

Knapp, Jr., Furn F. (Oak Ridge, TN); Lisic, Edward C. (Cookeville, TN); Mirzadeh, Saed (Knoxville, TN); Callahan, Alvin P. (Harriman, TN)

1993-01-01T23:59:59.000Z

50

Tungsten-188/carrier-free rhenium-188 perrhenic acid generator system  

DOE Patents (OSTI)

A generator system for providing a carrier-free radioisotope in the form of an acid comprises a chromatography column in tandem fluid connection with an ion exchange column, the chromatography column containing a charge of a radioactive parent isotope. The chromatography column, charged with a parent isotope, is eluted with an alkali metal salt solution to generate the radioisotope in the form of an intermediate solution, which is passed through the ion-exchange column to convert the radioisotope to a carrier-free acid form.

Knapp, Jr., Furn F. (Oak Ridge, TN); Lisic, Edward C. (Cookeville, TN); Mirzadeh, Saed (Knoxville, TN); Callahan, Alvin P. (Harriman, TN)

1994-01-01T23:59:59.000Z

51

Pyrolytic conversion of plastic and rubber waste to hydrocarbons with basic salt catalysts  

DOE Patents (OSTI)

The invention relates to a process for improving the pyrolytic conversion of waste selected from rubber and plastic to low molecular weight olefinic materials by employing basis salt catalysts in the waste mixture. The salts comprise alkali or alkaline earth compounds, particularly sodium carbonate, in an amount of greater than about 1 weight percent based on the waste feed.

Wingfield, Jr., Robert C. (Southfield, MI); Braslaw, Jacob (Southfield, MI); Gealer, Roy L. (West Bloomfield, MI)

1985-01-01T23:59:59.000Z

52

Non-Lead/Acid Battery Recyclers:  

Science Conference Proceedings (OSTI)

... in H2O solution such as Citric Acid, Acetic Acid, Acetates or ... MnO2 is soluble in sulfuric acid only at ... cells were treated by alkali followed by acids. ...

2011-08-02T23:59:59.000Z

53

SEPARATION OF PROTACTINIUM FROM MOLTEN SALT REACTOR FUEL COMPOSITIONS  

DOE Patents (OSTI)

A method for selectively precipitating protactinium from a neutron- irradiated fused fluoride salt composition comprising at least one metal fluoride selected from the group consisting of an alkali metal fluoride and an alkaline earth metal fluoride containing dissolved thorium-232 values is presented. An inorganic metal oxide corresponding to any of the metal fluorides of the composition is also added. (AEC)

Shaffer, J.H.; Strain, J.E.; Cuneo, D.R.; Kelly, M.J.

1963-11-12T23:59:59.000Z

54

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

55

Electrolytic orthoborate salts for lithium batteries  

DOE Patents (OSTI)

Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

Angell, Charles Austen (Mesa, AZ); Xu, Wu (Tempe, AZ)

2008-01-01T23:59:59.000Z

56

Iodized Salt  

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

Iodized Salt Iodized Salt Name: Theresa Location: N/A Country: N/A Date: N/A Question: Why do they put iodine in salt? Replies: Iodine was introduced into salt at earlier this century when it was discovered that certain areas of the US had a mark deficiency in iodine in the diet of people, and people developed a neck swelling (goiter). The Great Lakes region is one of these areas where the soil is lacking iodine. Goiter can be caused when the thyroid gland swells because of a lack of iodine in the diet. Most medical advise now states that iodine in salt is no longer necessary due to our food sources arising from all over the world. Steve Sample Hi Theresa...see, there are a variety of elements and compounds that are necessary for the proper maintenance of our life. One of these is iodine, since a small quantity of iodine is needed for the adequate functioning of the thyroid gland. A deficiency of iodine produces dire effects, as goiter, where the thyroid gland swollens due to the lack of iodine traces in the diet. The iodine affects directly the tyrhoid gland secretions, which themselves, to a great extent, control heart action, nerve response to stimuli, rate of body growth and metabolism.

57

Regenerable activated bauxite adsorbent alkali monitor probe  

DOE Patents (OSTI)

This invention relates to a regenerable activated bauxite adsorber alkali monitor probe for field applications to provide reliable measurement of alkali-vapor 5 concentration in combustion gas with special emphasis on pressurized fluidized-bed combustion (PFBC) off-gas. More particularly, the invention relates to the development of a easily regenerable bauxite adsorbent for use in a method to accurately determine the alkali-vapor content of PFBC 10 exhaust gases.

Lee, S.H.D.

1991-01-22T23:59:59.000Z

58

Regenerable activated bauxite adsorbent alkali monitor probe  

DOE Patents (OSTI)

A regenerable activated bauxite adsorber alkali monitor probe for field applications to provide reliable measurement of alkali-vapor concentration in combustion gas with special emphasis on pressurized fluidized-bed combustion (PFBC) off-gas. More particularly, the invention relates to the development of a easily regenerable bauxite adsorbent for use in a method to accurately determine the alkali-vapor content of PFBC exhaust gases. 6 figs.

Lee, S.H.D.

1992-12-22T23:59:59.000Z

59

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

60

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

Note: This page contains sample records for the topic "acids alkalies salts" 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

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

62

Method for removing semiconductor layers from salt substrates  

DOE Patents (OSTI)

A method is described for removing a CVD semiconductor layer from an alkali halide salt substrate following the deposition of the semiconductor layer. The semiconductor-substrate combination is supported on a material such as tungsten which is readily wet by the molten alkali halide. The temperature of the semiconductor-substrate combination is raised to a temperature greater than the melting temperature of the substrate but less than the temperature of the semiconductor and the substrate is melted and removed from the semiconductor by capillary action of the wettable support.

Shuskus, Alexander J. (West Hartford, CT); Cowher, Melvyn E. (East Brookfield, MA)

1985-08-27T23:59:59.000Z

63

Acrylic Acid from 3-Hydroxypropionic Acid - Energy Innovation ...  

Technology Marketing Summary. 3-hydroxypropionic acid is readily converted to acrylic acid by conversion to the acid salt followed by treatment with a solid oxide ...

64

Potentials for fuel cells in refineries and chlor-alkali plants  

DOE Green Energy (OSTI)

The market potentials for fuel cell cogeneration systems in petroleum refineries and chlor-alkali plants were evaluated. the most promising application appears to be in chlor-alkali plants where the production process is electricity intensive. Future anticipated changes in the production process are favorable to the use of fuel cells. The energy use in refineries is steam intensive with the required steam pressures ranging from approximately 15 to 650 psig. The near-term use of fuel cell cogeneration in refineries is not as attractive as in chlor-alkali plants. The phosphoric acid fuel cell is the most developed and the most competitive, but its use is limited by its being able to produce only low-pressure steam. Over the longer term, the molten carbonate and the solid oxide fuel cell both of which operate at significantly higher temperatures, are technically very attractive. However, they do not appear to be cost competitive with conventional systems.

Altseimer, J.H.; Roach, F.

1986-01-01T23:59:59.000Z

65

INTERACTION OF A SUB-BITUMINOUS COAL WITH A STRONG ACID AND A STRONG BASE  

E-Print Network (OSTI)

Investigation of Molten-Salt/Organic-Solvent CombinationsAs an alternative to molten salts, inorganic acids are aniii) Investigation of molten-salt/organic- Dee Extraction of

Seth, M.

2010-01-01T23:59:59.000Z

66

Selection of non-adsorbing alkali components  

Science Conference Proceedings (OSTI)

This project consists of three phases of laboratory experimental study. In phase I (screening), eight candidate materials, 304SS (serves as a base material for comparison), Hastelloy C-276, Hastelloy X, Haynes No. 188, Allonized 304SS, Pt-coated 304SS, and ceramic-coated 304SS, will be subjected to atmospheric TGA study under the simulated PFBC (oxidizing) environment with and without alkali vapor doping. Each candidate material will be evaluated for its resistance toward alkali-vapor capture. In addition, a post-test metallographic characterization of the sample will be performed to obtain a better understanding of the alkali capture mechanism and material behavior. The material(s) with little or no alkali-vapor adsorption will be selected as the promising material(s) for the Phase II study. In Phase II, the promising material(s) will be further tested in the TGA under elevated pressure to simulate the PFBC environment (in terms of temperature, pressure, and gas composition). The effect of pressure on the extent of alkali-vapor adsorption will be evaluated, and the test samples will be metallographically characterized. The most promising candidate material(s) will be identified and recommended for further tesfing in the actual PFBC environment. In Phase III, four materials will be selected from the eight candidate materials screened in the PFBC environment and will be evaluated for their alkali-vapor capture by atmospheric TGA under the coal gasification fuel gas (reducing) environment. The tested samples will also be metallographically characterized. The most promising material(s) will be identified and recommended for further testing in the actual coal gasification environment.

Lee, S.H.D.; Natesan, K.; Swift, W.M.

1992-11-01T23:59:59.000Z

67

Selection of non-adsorbing alkali components  

Science Conference Proceedings (OSTI)

This project consists of three phases of laboratory experimental study. In phase I (screening), eight candidate materials, 304SS (serves as a base material for comparison), Hastelloy C-276, Hastelloy X, Haynes No. 188, Allonized 304SS, Pt-coated 304SS, and ceramic-coated 304SS, will be subjected to atmospheric TGA study under the simulated PFBC (oxidizing) environment with and without alkali vapor doping. Each candidate material will be evaluated for its resistance toward alkali-vapor capture. In addition, a post-test metallographic characterization of the sample will be performed to obtain a better understanding of the alkali capture mechanism and material behavior. The material(s) with little or no alkali-vapor adsorption will be selected as the promising material(s) for the Phase II study. In Phase II, the promising material(s) will be further tested in the TGA under elevated pressure to simulate the PFBC environment (in terms of temperature, pressure, and gas composition). The effect of pressure on the extent of alkali-vapor adsorption will be evaluated, and the test samples will be metallographically characterized. The most promising candidate material(s) will be identified and recommended for further tesfing in the actual PFBC environment. In Phase III, four materials will be selected from the eight candidate materials screened in the PFBC environment and will be evaluated for their alkali-vapor capture by atmospheric TGA under the coal gasification fuel gas (reducing) environment. The tested samples will also be metallographically characterized. The most promising material(s) will be identified and recommended for further testing in the actual coal gasification environment.

Lee, S.H.D.; Natesan, K.; Swift, W.M.

1992-01-01T23:59:59.000Z

68

Petrography study on altered flint aggregate by alkali-silica reaction  

SciTech Connect

The aim of our study is to improve our understanding of an alkali-silica reaction (ASR) via petrography. We used a chemical concrete subsystem: flint aggregate, portlandite and KOH. The altered flint aggregate is followed by optical microscopy and scanning electron microscopy (SEM) before and after acid treatment at different intervals. After acid treatment, the observations showed an increase in aggregate porosity and revealed internal degradation of the aggregate. This degradation created amorphous zones. Before acid treatment, the analyses on polished sections by scanning electron microscopy coupled with energy dispersive spectroscopy (EDS) enabled visualization of K{sup +} and Ca{sup 2+} penetration into the aggregate. The appearance of amorphous zones and penetration of positive ions into the aggregate are correlated with the increase in the molar fraction of silanol sites. This degradation is specific to the alkali-silica reaction.

Bulteel, D. [Departement Genie Civil de l'Ecole Nationale Superieure des Techniques Industrielles et des Mines de Douai, 941 rue Charles Bourseul, B.P. 838, F-59508, DOUAI Cedex (France)]. E-mail: bulteel@ensm-douai.fr; Rafai, N. [Laboratoire d'Etude et de Recherches des Materiaux a Arles, F-13631 ARLES (France); Degrugilliers, P. [Departement Genie Civil de l'Ecole Nationale Superieure des Techniques Industrielles et des Mines de Douai, 941 rue Charles Bourseul, B.P. 838, F-59508, DOUAI Cedex (France); Garcia-Diaz, E. [Departement Genie Civil de l'Ecole Nationale Superieure des Techniques Industrielles et des Mines de Douai, 941 rue Charles Bourseul, B.P. 838, F-59508, DOUAI Cedex (France)

2004-11-15T23:59:59.000Z

69

METATHESIS OF PLUTONIUM CARRIER LANTHANUM FLUORIDE PRECIPITATE WITH AN ALKALI  

DOE Patents (OSTI)

A plutonium fluoride precipitate is converted to plutonium hydroxide by digesting the precipitate with an aqueous alkali metal hydroxide solution.

Duffield, R.B.

1960-04-01T23:59:59.000Z

70

A Primitive Alkali Basaltic Stratovolcano And Associated Eruptive Centres,  

Open Energy Info (EERE)

Primitive Alkali Basaltic Stratovolcano And Associated Eruptive Centres, Primitive Alkali Basaltic Stratovolcano And Associated Eruptive Centres, Northwestern Spitsbergen- Volcanology And Tectonic Significance Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: A Primitive Alkali Basaltic Stratovolcano And Associated Eruptive Centres, Northwestern Spitsbergen- Volcanology And Tectonic Significance Details Activities (0) Areas (0) Regions (0) Abstract: Three Quaternary volcanic centres (Sverrefjell, Sigurdfjell and Halvdanpiggen) in northwestern Spitsbergen formed by off-ridge alkali basaltic volcanism associated with nearby ocean-floor spreading and subsequent tectonism. The Sverrefjell volcano is a unique stratovolcano constructed of primitive alkali basaltic pyroclastics with subordinate lavas. About 15-20 vol.% of this volcanic (and the other centres) comprises

71

Alkali metal recovery from carbonaceous material conversion 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 in the gasifier or similar reaction zone, alkali metal constitutents are recovered from the particles by withdrawing and passing the particles from the reaction zone to an alkali metal recovery zone in the substantial absence of molecular oxygen and treating the particles in the recovery zone with water or an aqueous solution in the substantial absence of molecular oxygen. The solution formed by treating the particles in the recovery zone will contain water-soluble alkali metal constituents and is recycled to the conversion process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst. Preventing contact of the particles with oxygen as they are withdrawn from the reaction zone and during treatment in the recovery zone avoids the formation of undesirable alkali metal constituents in the aqueous solution produced in the recovery zone and insures maximum recovery of water-soluble alkali metal constituents from the alkali metal residues.

Sharp, David W. (Seabrook, TX); Clavenna, LeRoy R. (Baytown, TX); Gorbaty, Martin L. (Fanwood, NJ); Tsou, Joe M. (Galveston, TX)

1980-01-01T23:59:59.000Z

72

PRODUCTION OF TRIFLUOROACETIC ACID  

DOE Patents (OSTI)

A method is given for the production of improved yields of trifluoroacetic acid. The compound is prepared by oxidizing m-aminobenzotrifluoride with an alkali metal or alkaline earth metal permanganate at a temperature in the range of 80 deg C to 100 deg C while dissolved ln a mixture of water with glacial acetic acid and/or trifluoroacetic acid. Preferably a mixture of water and trifluoroacetic acid ls used as the solvent.

Haworth, W.N.; Stacey, M.

1949-07-19T23:59:59.000Z

73

Molten salt electrolyte separator  

DOE Patents (OSTI)

A molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication.

Kaun, Thomas D. (New Lenox, IL)

1996-01-01T23:59:59.000Z

74

Salt transport extraction of transuranium elements from lwr fuel  

DOE Patents (OSTI)

A process of separating transuranium actinide values from uranium values present in spent nuclear oxide fuels which contain rare earth and noble metal fission products. The oxide fuel is reduced with Ca metal in the presence of CaCl.sub.2 and a Cu--Mg alloy containing not less than about 25% by weight Mg at a temperature in the range of from about 750.degree. C. to about 850.degree. C. to precipitate uranium metal and some of the noble metal fission products leaving the Cu--Mg alloy having transuranium actinide metals and rare earth fission product metals and some of the noble metal fission products dissolved therein. The CaCl.sub.2 having CaO and fission products of alkali metals and the alkali earth metals and iodine dissolved therein is separated and electrolytically treated with a carbon electrode to reduce the CaO to Ca metal while converting the carbon electrode to CO and CO.sub.2. The Ca metal and CaCl.sub.2 is recycled to reduce additional oxide fuel. The Cu--Mg alloy having transuranium metals and rare earth fission product metals and the noble metal fission products dissolved therein is contacted with a transport salt including Mg Cl.sub.2 to transfer Mg values from the transport salt to the Cu--Mg alloy while transuranium actinide and rare earth fission product metals transfer from the Cu--Mg alloy to the transport salt. Then the transport salt is mixed with a Mg--Zn alloy to transfer Mg values from the alloy to the transport salt while the transuranium actinide and rare earth fission product values dissolved in the salt are reduced and transferred to the Mg--Zn alloy.

Pierce, R. Dean (Naperville, IL); Ackerman, John P. (Downers Grove, IL); Battles, James E. (Oak Forest, IL); Johnson, Terry R. (Wheaton, IL); Miller, William E. (Naperville, IL)

1992-01-01T23:59:59.000Z

75

Salt transport extraction of transuranium elements from LWR fuel  

DOE Patents (OSTI)

A process is described for separating transuranium actinide values from uranium values present in spent nuclear oxide fuels which contain rare earth and noble metal fission products. The oxide fuel is reduced with Ca metal in the presence of CaCl[sub 2] and a Cu--Mg alloy containing not less than about 25% by weight Mg at a temperature in the range of from about 750 C to about 850 C to precipitate uranium metal and some of the noble metal fission products leaving the Cu--Mg alloy having transuranium actinide metals and rare earth fission product metals and some of the noble metal fission products dissolved therein. The CaCl[sub 2] having CaO and fission products of alkali metals and the alkali earth metals and iodine dissolved therein is separated and electrolytically treated with a carbon electrode to reduce the CaO to Ca metal while converting the carbon electrode to CO and CO[sub 2]. The Ca metal and CaCl[sub 2] is recycled to reduce additional oxide fuel. The Cu--Mg alloy having transuranium metals and rare earth fission product metals and the noble metal fission products dissolved therein is contacted with a transport salt including MgCl[sub 2] to transfer Mg values from the transport salt to the Cu--Mg alloy while transuranium actinide and rare earth fission product metals transfer from the Cu--Mg alloy to the transport salt. Then the transport salt is mixed with a Mg--Zn alloy to transfer Mg values from the alloy to the transport salt while the transuranium actinide and rare earth fission product values dissolved in the salt are reduced and transferred to the Mg--Zn alloy. 2 figs.

Pierce, R.D.; Ackerman, J.P.; Battles, J.E.; Johnson, T.R.; Miller, W.E.

1992-11-03T23:59:59.000Z

76

Salt transport extraction of transuranium elements from LWR fuel  

DOE Patents (OSTI)

This report discusses a process of separating transuranium actinide values from uranium values present in spent nuclear oxide fuels which contain rare earth and noble metal fission products. The oxide fuel is reduced with Ca metal in the presence of CaCl{sub 2} and a Cu-Mg alloy containing not less than about 25% by weight Mg at a temperature in the range of from about 750{degrees}C to about 850{degrees}C to precipitate uranium metal and some of the noble metal fission products leaving the Cu-Mg alloy having transuranium actinide metals and rare earth fission product metals and some of the noble metal fission products dissolved therein. The CaCl{sub 2} having Cao and fission products of alkali metals and the alkali earth metals and iodine dissolved therein is separated and electrolytically treated with a carbon electrode to reduce the CaO to Ca metal while converting the carbon electrode to CO and CO{sub 2}. The Ca metal and CaCl{sub 2} is recycled to reduce additional oxide fuel. The Cu-Mg alloy having transuranium metals and rare earth fission product metals and the noble metal fission products dissolved therein is contacted with a transport salt including Mg C1{sub 2} to transfer Mg values from the transport salt to the Cu-Mg alloy .hile transuranium actinide and rare earth fission product metals transfer from the Cu-Mg alloy to the transport salt. Then the transport salt is mixed with a Mg-Zn alloy to transfer Mg values from the alloy to the transport salt while the transuranium actinide and rare earth fission product values dissolved in the salt are reduced and transferred to the Mg-Zn alloy.

Pierce, R.D.; Ackerman, J.P.; Battles, J.E.; Johnson, T.R.; Miller, W.E.

1991-12-31T23:59:59.000Z

77

Removal of Retired Alkali Metal Test Systems  

SciTech Connect

This paper describes the successful effort to remove alkali metals, alkali metal residues, and piping and structures from retired non-radioactive test systems on the Hanford Site. These test systems were used between 1965 and 1982 to support the Fast Flux Test Facility and the Liquid Metal Fast Breeder Reactor Program. A considerable volume of sodium and sodium-potassium alloy (NaK) was successfully recycled to the commercial sector; structural material and electrical material such as wiring was also recycled. Innovative techniques were used to safely remove NaK and its residues from a test system that could not be gravity-drained. The work was done safely, with no environmental issues or significant schedule delays.

Brehm, W. F.; Church, W. R.; Biglin, J. W.

2003-02-26T23:59:59.000Z

78

Alkali metal protective garment and composite material  

DOE Patents (OSTI)

A protective garment and composite material providing satisfactory heat resistance and physical protection for articles and personnel exposed to hot molten alkali metals, such as sodium. Physical protection is provided by a continuous layer of nickel foil. Heat resistance is provided by an underlying backing layer of thermal insulation. Overlying outer layers of fireproof woven ceramic fibers are used to protect the foil during storage and handling.

Ballif, III, John L. (Salt Lake City, UT); Yuan, Wei W. (Seattle, WA)

1980-01-01T23:59:59.000Z

79

acid  

Office of Legacy Management (LM)

Acid/Pueblo Canyon, New Mexico, Site is Acid/Pueblo Canyon, New Mexico, Site is located near the town of Los Alamos, New Mexico, approximately 25 miles northwest of Santa Fe and 60 miles north-northeast of Albuquerque. The site is accessible from Canyon Road, which runs just south of the former waste treatment plant. The plant was situated on a mesa that forms the south rim of Acid Canyon. Acid Canyon is a small tributary near the head

80

A PRELIMINARY STUDY OF MOLTEN SALT POWER REACTORS  

SciTech Connect

A preliminary study of molten salt pcwer reactors was made. The most promising fuel carrier salts were the fluorides and chlorides of the alkali metals, zirconium, and beryllium. The chlorides were found to have lower melting points but were less stable and more corrosive than the fluorides. A Li/sup 7/ F- - BeF/sub 2/ mixture with ThF/sub 4/ and UF/sub 4/appeared to perform best. Of the numerous alloys tested as container material, Inconel and a nickel-- molybdenum alloy INOR-8 appeared to be the most resistant to corrosion. To study the performance, safety, economics, and construction costs of a typical molten salt reactor, a reactor of specific type and size was chosen for study. The reference design reactor was a two-region homogeneous converter with a core salt of 70 mole% Li/sup 7/F and 30% BeF/sub 2. ThF/sub 4/ and enough VF/sub 4/ for criticality were added. Study in- dicated that a molten salt reactor would prcduce economical power, but the problem of developing a salt core and a container metal which would last for mamy years of operation needed further study. (M.C.G.)

MacPherson, H.G.; Alexander, L.G.; Carrison, D.A.; Estabrook, J.Y.; Kinyon, B.W.; Mann, L.A.; Roberts, J.T.; Romie, F.E.; VonderLage, F.C.

1957-04-29T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Sorption of carboxylic acid from carboxylic salt solutions at pHs close to or above the pK[sub a] of the acid, with regeneration with an aqueous solution of ammonia or low-molecular-weight alkylamine  

DOE Patents (OSTI)

Carboxylic acids are sorbed from aqueous feedstocks at pHs close to or above the acids' pH[sub a] into a strongly basic organic liquid phase or onto a basic solid adsorbent or moderately basic ion exchange resin. The acids are freed from the sorbent phase by treating it with aqueous alkylamine or ammonia thus forming an alkylammonium or ammonium carboxylate which dewatered and decomposed to the desired carboxylic acid and the alkylamine or ammonia. 8 figs.

King, C.J.; Tung, L.A.

1992-07-21T23:59:59.000Z

82

Electrochemical devices utilizing molten alkali metal electrode-reactant  

DOE Patents (OSTI)

Electrochemical cells are provided with a reactive metal to reduce the oxide of the alkali metal electrode-reactant. Cells employing a molten alkali metal electrode, e.g., sodium, in contact with a ceramic electrolyte, which is a conductor of the ions of the alkali metal forming the electrode, exhibit a lower resistance when a reactive metal, e.g., vanadium, is allowed to react with and reduce the alkali metal oxide. Such cells exhibit less degradation of the electrolyte and of the glass seals often used to joining the electrolyte to the other components of the cell under cycling conditions.

Hitchcock, D.C.; Mailhe, C.C.; De Jonghe, L.C.

1985-07-10T23:59:59.000Z

83

Neutral Oil Loss During Alkali Refining - ResearchGate  

U.S. Energy Information Administration (EIA)

Neutral Oil Loss During Alkali Refining. Albert J. Dijkstra. Journal of Oil & Fat Industries (Impact ... Experiments with cotton oil and soybean o ...

84

acid  

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

Acid/Pueblo Canyon, New Mexico, Site. Acid/Pueblo Canyon, New Mexico, Site. This site is managed by the U.S. Department of Energy Office of Legacy Management. Site Description and History The Acid/Pueblo Canyon, New Mexico, Site is located near the town of Los Alamos, New Mexico, approximately 25 miles northwest of Santa Fe and 60 miles north-northeast of Albuquerque. The site is accessible from Canyon Road, which runs just south

85

An Overview of Liquid Fluoride Salt Heat Transport Systems  

SciTech Connect

Heat transport is central to all thermal-based forms of electricity generation. The ever increasing demand for higher thermal efficiency necessitates power generation cycles transitioning to progressively higher temperatures. Similarly, the desire to provide direct thermal coupling between heat sources and higher temperature chemical processes provides the underlying incentive to move toward higher temperature heat transfer loops. As the system temperature rises, the available materials and technology choices become progressively more limited. Superficially, fluoride salts at {approx}700 C resemble water at room temperature being optically transparent and having similar heat capacity, roughly three times the viscosity, and about twice the density. Fluoride salts are a leading candidate heat-transport material at high temperatures. Fluoride salts have been extensively used in specialized industrial processes for decades, yet they have not entered widespread deployment for general heat transport purposes. This report does not provide an exhaustive screening of potential heat transfer media and other high temperature liquids such as alkali metal carbonate eutectics or chloride salts may have economic or technological advantages. A particular advantage of fluoride salts is that the technology for their use is relatively mature as they were extensively studied during the 1940s-1970s as part of the U.S. Atomic Energy Commission's program to develop molten salt reactors (MSRs). However, the instrumentation, components, and practices for use of fluoride salts are not yet developed sufficiently for commercial implementation. This report provides an overview of the current understanding of the technologies involved in liquid salt heat transport (LSHT) along with providing references to the more detailed primary information resources. Much of the information presented here derives from the earlier MSR program. However, technology has evolved over the intervening years, and this report also describes more recently developed technologies such as dry gas seals. This report also provides a high-level, parametric evaluation of LSHT loop performance to allow general intercomparisons between heat-transport fluid options as well as provide an overview of the properties and requirements for a representative loop. A compilation of relevant thermophysical properties of useful fluoride salts is also included for salt heat transport systems. Fluoride salts can be highly corrosive depending on the container materials selected, the salt chemistry, and the operating procedures used. The report includes an overview of the state-of-the-art in reduction-oxidation chemistry control methodologies employed to minimize corrosion issues. Salt chemistry control technology, however, remains at too low a level of understanding for widespread industrial usage. Loop operational issues such as start-up procedures and system freeze-up vulnerability are also discussed. Liquid fluoride salts are a leading candidate heat transport medium for high-temperature applications. This report provides an overview of the current status of liquid salt heat transport technology. The report includes a high-level, parametric evaluation of liquid fluoride salt heat transport loop performance to allow intercomparisons between heat-transport fluid options as well as providing an overview of the properties and requirements for a representative loop. Much of the information presented here derives from the earlier molten salt reactor program and a significant advantage of fluoride salts, as high temperature heat transport media is their consequent relative technological maturity. The report also includes a compilation of relevant thermophysical properties of useful heat transport fluoride salts. Fluoride salts are both thermally stable and with proper chemistry control can be relatively chemically inert. Fluoride salts can, however, be highly corrosive depending on the container materials selected, the salt chemistry, and the operating procedures used. The report also provides an over

Holcomb, David Eugene [ORNL; Cetiner, Mustafa Sacit [ORNL

2010-09-01T23:59:59.000Z

86

Leach resistance properties and release processes for salt-occluded zeolite A  

SciTech Connect

The pyrometallurgical processing of spent fuel from the Integral Fast Reactor (IFR) results in a waste of LiCl-KCl-NaCl salt containing approximately 10 wt% fission products, primarily CsCl and SrCl[sub 2]. For disposal, this waste must be immobilized in a form that it is leach resistant. A salt-occluded zeolite has been identified as a potential waste form for the salt. Its leach resistance properties were investigated using powdered samples. The results were that strontium was not released and cesium had a low release, 0.056 g/m[sup 2] for the 56 day leach test. The initial release (within 7 days) of alkali metal cations was rapid and subsequent releases were much smaller. The releases of aluminum and silicon were 0.036 and 0.028 g/m[sup 2], respectively, and were constant. Neither alkali metal cation hydrolysis nor exchange between cations in the leachate and those in the zeolite was significant. Only sodium release followed t[sup 0.5] kinetics. Selected dissolution of the occluded salt was the primary release process. These results confirm that salt-occluded zeolite has promise as the waste form for IFR pyroprocess salt.

Lewis, M.A.; Fischer, D.F.; Laidler, J.J.

1992-01-01T23:59:59.000Z

87

Leach resistance properties and release processes for salt-occluded zeolite A  

SciTech Connect

The pyrometallurgical processing of spent fuel from the Integral Fast Reactor (IFR) results in a waste of LiCl-KCl-NaCl salt containing approximately 10 wt% fission products, primarily CsCl and SrCl{sub 2}. For disposal, this waste must be immobilized in a form that it is leach resistant. A salt-occluded zeolite has been identified as a potential waste form for the salt. Its leach resistance properties were investigated using powdered samples. The results were that strontium was not released and cesium had a low release, 0.056 g/m{sup 2} for the 56 day leach test. The initial release (within 7 days) of alkali metal cations was rapid and subsequent releases were much smaller. The releases of aluminum and silicon were 0.036 and 0.028 g/m{sup 2}, respectively, and were constant. Neither alkali metal cation hydrolysis nor exchange between cations in the leachate and those in the zeolite was significant. Only sodium release followed t{sup 0.5} kinetics. Selected dissolution of the occluded salt was the primary release process. These results confirm that salt-occluded zeolite has promise as the waste form for IFR pyroprocess salt.

Lewis, M.A.; Fischer, D.F.; Laidler, J.J.

1992-12-31T23:59:59.000Z

88

Post-Harvest Processing Methods for Reduction of Silica and Alkali Metals in Wheat Straw  

SciTech Connect

Silica and alkali metals in wheat straw limit its use for bioenergy and gasification. Slag deposits occur via the eutectic melting of SiO2 with K2O, trapping chlorides at surfaces and causing corrosion. A minimum melting point of 950°C is desirable, corresponding to SiO2:K2O of about 3:1. Mild chemical treatments were used to reduce Si, K, and Cl, while varying temperature, concentration, %-solids, and time. Dilute acid was more effective at removing K and Cl, while dilute alkali was more effective for Si. Reduction of minerals in this manner may prove economical for increasing utilization of the straw for combustion or gasification.

Thompson, David Neal; Lacey, Jeffrey Alan; Shaw, Peter Gordon

2002-04-01T23:59:59.000Z

89

Amine salts of nitroazoles  

DOE Patents (OSTI)

Compositions of matter, a method of providing chemical energy by burning said compositions, and methods of making said compositions. These compositions are amine salts of nitroazoles.

Lee, Kien-yin (Los Alamos, NM); Stinecipher, Mary M. (Los Alamos, NM)

1993-01-01T23:59:59.000Z

90

Recovery of alkali metal constituents from catalytic coal conversion residues  

DOE Patents (OSTI)

In a coal gasification operation (32) or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein particles containing alkali metal residues are produced, alkali metal constituents are recovered from the particles by contacting them (46, 53, 61, 69) with water or an aqueous solution to remove water-soluble alkali metal constituents and produce an aqueous solution enriched in said constituents. The aqueous solution thus produced is then contacted with carbon dioxide (63) to precipitate silicon constituents, the pH of the resultant solution is increased (81), preferably to a value in the range between about 12.5 and about 15.0, and the solution of increased pH is evaporated (84) to increase the alkali metal concentration. The concentrated aqueous solution is then recycled to the conversion process (86, 18, 17) where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst.

Soung, Wen Y. (Houston, TX)

1984-01-01T23:59:59.000Z

91

COMPLEX FLUORIDES OF PLUTONIUM AND AN ALKALI METAL  

DOE Patents (OSTI)

A method is given for precipitating alkali metal plutonium fluorides. such as KPuF/sub 5/, KPu/sub 2/F/sub 9/, NaPuF/sub 5/, and RbPuF/sub 5/, from an aqueous plutonium(IV) solution by adding hydrogen fluoride and alkali-metal- fluoride.

Seaborg, G.T.

1960-08-01T23:59:59.000Z

92

Molten salt electrolyte separator  

DOE Patents (OSTI)

The patent describes a molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication. 5 figs.

Kaun, T.D.

1996-07-09T23:59:59.000Z

93

Tuning of the Metal-Insulator Transition via Alkali Adsorption  

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

Tuning of the Metal-Insulator Transition via Alkali Adsorption Print Tuning of the Metal-Insulator Transition via Alkali Adsorption Print Turning a material from an insulator to a metal, or vice versa, by light irradiation, exposure to electric or magnetic fields, or applying small changes in temperature, pressure, or doping-such intriguing control of a material's electronic properties is possible by exploiting strongly interacting or "correlated" electrons. Now a team of researchers from the University of Kiel in Germany and the ALS has found a novel, surprising way to continuously transform a layered metallic transition-metal compound, TaS2, into an insulator. Using angle-resolved photoemission spectroscopy (ARPES), they have demonstrated that adsorption of alkali atoms onto this material's surface gradually makes it more insulating, although in general, alkali adsorption should lead to more metallic behavior, as alkali atoms easily give away their loosely bound outermost electron.

94

Solution-Derived, Chloride-Containing Minerals as a Waste Form for Alkali Chlorides  

SciTech Connect

Sodalite [Na8(AlSiO4)6Cl2] and cancrinite [(Na,K)6Ca2Al6Si6O24Cl4] are environmentally stable, chloride-containing minerals and are a logical waste form option for the mixed alkali chloride salt waste stream that is generated from a proposed electrochemical separations process during nuclear fuel reprocessing. Due to the volatility of chloride salts at moderate temperatures, the ideal processing route for these salts is a low-temperature approach such as the sol-gel process. The sodalite structure can be easily synthesized by the sol-gel process; however, it is produced in the form of a fine powder with particle sizes on the order of 1–10 µm. Due to the small particle size, these powders require additional treatment to form a monolith. In this study, the sol-gel powders were pressed into pellets and fired to achieve > 90% of theoretical density. The cancrinite structure, identified as the best candidate mineral form in terms of waste loading capacity, was only produced on a limited basis following the sol-gel process and converted to sodalite upon firing. Here we discuss the sol-gel process specifics, chemical durability of select waste forms, and the steps taken to maximize chloride-containing phases, decrease chloride loss during pellet firing, and increase pellet densities.

Riley, Brian J.; Crum, Jarrod V.; Matyas, Josef; McCloy, John S.; Lepry, William C.

2012-10-01T23:59:59.000Z

95

Microbiological, sensory, color and chemical characteristics of vacuum-packaged ground beef patties and cooked beef top rounds treated with the salts of various organic acids  

E-Print Network (OSTI)

The study was conducted in two phases. In Phase 1, vacuum-packaged ground beef patties containing sodium lactate, sodium propionate, sodium acetate and sodium citrate at various levels and combinations were stored up to 28 days at 4'C. Addition of sodium lactate alone or in combination with sodium propionate increased the shelf life of the patties by decreasing microbiological growth, decreasing negative flavor notes associated with lipid oxidation and decreasing water activity. Lean color of the patties also was improved by the addition of sodium lactate alone or in combination with sodium propionate. Lipid oxidation as measured by TBA (2-thiobarbituric acid) analysis was unaffected by treatment addition. In Phase 11, cooked vacuum-packaged beef top rounds containing 3% sodium lactate or 3 or 4% sodium lactate in combination with 0. 1 or 0.2% sodium propionate were stored for up to 84 days at 4'C. Addition of any of the treatments to the roasts in this phase greatly reduced total APCs (Aerobic Plate Counts). Positive flavor notes associated with fresh beef were enhanced by ingredient addition and tended to be highest in roasts containing 3% sodium lactate + 0.2% sodium propionate. Cooked roast beef color was enhanced by the additon of sodium lactate alone or in combination with 0. I % sodium propionate. Lipid oxidation and water activity were decreased by the addition of sodium lactate in combination with sodium propionate and pH and cooked yield were increased with any level and combination of ingredient addition.

Maca, Jennifer Vahalik

1995-01-01T23:59:59.000Z

96

Potentials for Fuel Cells in Refineries and Chlor-Alkali Plants  

E-Print Network (OSTI)

The market potentials for fuel cell cogeneration systems in petroleum refineries and chlor-alkali plants were evaluated. Costs of the total energy consumed (power plus steam) were calculated and compared with those for more conventional cogeneration systems. Questionnaires were sent to major plants in both industries to determine technical requirements and data required for the assessment of the market potential. The most promising application appears to be in chlor-alkali plants where the production process is electricity intensive. Future anticipated changes in the production process are favorable to the use of fuel cells. The energy use in refineries is steam intensive with the required steam pressures ranging from approximately 15 to 650 psig. The near-term use of fuel cell cogeneration in refineries is not as attractive as in chlor-alkali plants. The phosphoric acid fuel cell is the most developed and the most cost competitive, but its use is limited by its being able to produce only low-pressure steam. Over the longer term, the molten carbonate and the solid oxide fuel cell, both of which operate at significantly higher temperatures, are technically very attractive. However, they do not appear to be cost competitive with conventional systems.

Altseimer, J. H.; Roach, F.

1986-06-01T23:59:59.000Z

97

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

98

Dual alkali approaches for the capture and separation of CO{sub 2}  

SciTech Connect

The Solvay process utilizes two alkalis in sequential order to convert CO{sub 2} to sodium carbonate for commercial use. The ability to transform CO{sub 2} into sodium carbonate cost-effectively would be a breakthrough in CO{sub 2} sequestration by providing benign long-term storage of CO{sub 2}. However, the Solvay process was not designed for CO{sub 2} sequestration and is not practical for use in the sequestration of CO{sub 2} from fossil fuel power plants. This paper investigates methods to modify the process in order to make it effective for the control of power plant CO{sub 2} emissions. The new modified process, called the Dual Alkali Approach, attempts to replace either or both bases, ammonia and lime, in the Solvay process with other compounds to make CO{sub 2} capture and separation efficient. Ammonia was replaced with different amines in aqueous solutions of salts and it was found that bicarbonate precipitation did occur. A method to regenerate the amine in the second step has not been implemented. However, the second step in Solvay Process has been implemented without using lime, namely, ammonia has been regenerated from an ammonium chloride solution using activated carbon. The HCl adsorbed in the activated carbon was removed by water to regenerate the activated carbon.

Huang, H.P.; Shi, Y.; Li, W.; Chang, S.G.

2000-04-04T23:59:59.000Z

99

Molten salt test loop  

DOE Green Energy (OSTI)

The objective of the Molten Salt Test Loop Project was to design, construct, and demonstrate operation of an outdoor high temperature molten salt test facility. This facility is operational, and can now be used to evaluate materials and components, and the design features and operating procedures required for molten salt heat transport systems. The initial application of the loop was to demonstrate the feasibility of using molten salt as the heat transport medium for a high temperature distributed collector system. A commercially available eutectic salt blend is used as the heat transfer fluid. This salt has a composition of 40% NaNO/sub 2/, 7% NaNO/sub 3/, and 53% KNO/sub 3/ and is marketed under the trade name Hitec. It has a freezing (solidifying) point of 142/sup 0/C (288/sup 0/F) and has been satisfactorily used at temperatures as high as 594/sup 0/C (1100/sup 0/F). General Atomic (GA) installed a row of Fixed Mirror Solar Concentrators (FMSC's) in the loop. The system was started up and a test program conducted. Startup went smoothly, with the exception of some burned-out trace heaters. Salt temperatures as high as 571/sup 0/C (1060/sup 0/F) were achieved.

Schuster, J.R.; Eggers, G.H.

1980-01-01T23:59:59.000Z

100

Salt Waste Processing Initiatives  

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

Patricia Suggs Patricia Suggs Salt Processing Team Lead Assistant Manager for Waste Disposition Project Office of Environmental Management Savannah River Site Salt Waste Processing Initiatives 2 Overview * Current SRS Liquid Waste System status * Opportunity to accelerate salt processing - transformational technologies - Rotary Microfiltration (RMF) and Small Column Ion Exchange (SCIX) - Actinide Removal Process/Modular Caustic Side Solvent Extraction (ARP/MCU) extension with next generation extractant - Salt Waste Processing Facility (SWPF) performance enhancement - Saltstone enhancements * Life-cycle impacts and benefits 3 SRS Liquid Waste Total Volume >37 Million Gallons (Mgal) Total Curies 183 MCi (51% ) 175 MCi (49% ) >358 Million Curies (MCi) Sludge 34.3 Mgal (92% ) 3.0 Mgal (8%)

Note: This page contains sample records for the topic "acids alkalies salts" 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

Amine salts of nitroazoles  

DOE Patents (OSTI)

Compositions of matter, a method of providing chemical energy by burning said compositions, and methods of making said compositions are described. These compositions are amine salts of nitroazoles. 1 figure.

Kienyin Lee; Stinecipher, M.M.

1993-10-26T23:59:59.000Z

102

Electrochemical cell utilizing molten alkali metal electrode-reactant  

DOE Patents (OSTI)

An improved electrochemical cell comprising an additive-modified molten alkali metal electrode-reactant and/or electrolyte is disclosed. Various electrochemical cells employing a molten alkali metal, e.g., sodium, electrode in contact with a cationically conductive ceramic membrane experience a lower resistance and a lower temperature coefficient of resistance whenever small amounts of selenium are present at the interface of the electrolyte and the molten alkali metal. Further, cells having small amounts of selenium present at the electrolyte-molten metal interface exhibit less degradation of the electrolyte under long term cycling conditions.

Virkar, Anil V. (Sandy, UT); Miller, Gerald R. (Salt Lake City, UT)

1983-11-04T23:59:59.000Z

103

Controlled temperature expansion in oxygen production by molten alkali metal salts  

DOE Patents (OSTI)

A continuous process is set forth for the production of oxygen from an oxygen containing gas stream, such as air, by contacting a feed gas stream with a molten solution of an oxygen acceptor to oxidize the acceptor and cyclically regenerating the oxidized acceptor by releasing oxygen from the acceptor wherein the oxygen-depleted gas stream from the contact zone is treated sequentially to temperature reduction by heat exchange against the feed stream so as to condense out entrained oxygen acceptor for recycle to the process, combustion of the gas stream with fuel to elevate its temperature and expansion of the combusted high temperature gas stream in a turbine to recover power. 1 fig.

Erickson, D.C.

1985-06-04T23:59:59.000Z

104

Controlled temperature expansion in oxygen production by molten alkali metal salts  

SciTech Connect

A continuous process is set forth for the production of oxygen from an oxygen containing gas stream, such as air, by contacting a feed gas stream with a molten solution of an oxygen acceptor to oxidize the acceptor and cyclically regenerating the oxidized acceptor by releasing oxygen from the acceptor wherein the oxygen-depleted gas stream from the contact zone is treated sequentially to temperature reduction by heat exchange against the feed stream so as to condense out entrained oxygen acceptor for recycle to the process, combustion of the gas stream with fuel to elevate its temperature and expansion of the combusted high temperature gas stream in a turbine to recover power.

Erickson, Donald C. (Annapolis)

1985-06-04T23:59:59.000Z

105

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

SciTech Connect

This report details the pyrometallurgical process for recycling spent metal fuels from the Integral Fast Reactor (IFR) which involves electrorefining spent fuel in a molten salt electrolyte (LiCl-KCI-U/PuCl{sub 3}) at 500{degree}C. The total heavy metal chloride concentration in the salt will be about 2 mol %. At some point, the concentrations of alkali, alkaline earth, and rare earth fission products in the salt must be reduced to lower the amount of heat generated in the electrorefiner. The heavy metal concentration in the salt must be reduced before removing the fission products from the salt. The operation uses a lithium-cadmium alloy anode that is solid at 500{degree}C, a solid mandrel cathode with a ceramic catch crucible below to collect heavy metal that falls off it, and a liquid cadmium cathode. The design criteria that had to be met by this equipment included the following: (1) control of the reduction rate by lithium, (2) good separation between heavy metal and rare earths, and (3) the capability to collect heavy metal and rare earths over a wide range of salt compositions. In tests conducted in an engineering-scale electrorefiner (10 kg uranium per cathode), good separation was achieved while removing uranium and rare earths from the salt. Only 13% of the rare earths was removed, while 99.9% of the uranium in the salt was removed; subsequently, the rare earths were also reduced to low concentrations. The uranium concentration in the salt was reduced to 0.05 ppm after uranium and rare earths were transferred from the salt to a solid mandrel cathode with a catch crucible. Rare earth concentrations in the salt were reduced to less than 0.01 wt % in these operations. Similar tests are planned to remove plutonium from the salt in a laboratory-scale (100--300 g heavy metal) electrorefiner.

Gay, E.C.; Miller, W.E.; Laidler, J.J.

1994-02-01T23:59:59.000Z

106

Salt Selected (FINAL)  

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

WHY SALT WAS SELECTED AS A DISPOSAL MEDIUM WHY SALT WAS SELECTED AS A DISPOSAL MEDIUM Waste Isolation Pilot Plant U.S. Department Of Energy Government officials and scientists chose the Waste Isolation Pilot Plant (WIPP) site through a selection process that started in the 1950s. At that time, the National Academy of Sciences conducted a nationwide search for geological formations stable enough to contain radioactive wastes for thousands of years. In 1955, after extensive

107

Electrodialysis-based separation process for salt recovery and recycling from waste water  

DOE Patents (OSTI)

A method for recovering salt from a process stream containing organic contaminants is provided, comprising directing the waste stream to a desalting electrodialysis unit so as to create a concentrated and purified salt permeate and an organic contaminants-containing stream, and contacting said concentrated salt permeate to a water-splitting electrodialysis unit so as to convert the salt to its corresponding base and acid. 6 figs.

Tsai, S.P.

1997-07-08T23:59:59.000Z

108

Gabbs Alkali Flat Geothermal Area | Open Energy Information  

Open Energy Info (EERE)

Gabbs Alkali Flat Geothermal Area Gabbs Alkali Flat Geothermal Area (Redirected from Gabbs Alkali Flat Area) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Geothermal Resource Area: Gabbs Alkali Flat Geothermal Area Contents 1 Area Overview 2 History and Infrastructure 3 Regulatory and Environmental Issues 4 Exploration History 5 Well Field Description 6 Geology of the Area 7 Geofluid Geochemistry 8 NEPA-Related Analyses (0) 9 Exploration Activities (2) 10 References Area Overview Geothermal Area Profile Location: Nevada Exploration Region: Walker-Lane Transition Zone Geothermal Region GEA Development Phase: 2008 USGS Resource Estimate Mean Reservoir Temp: Estimated Reservoir Volume: Mean Capacity: Click "Edit With Form" above to add content History and Infrastructure Operating Power Plants: 0

109

AN ANNOTATED BIBLIOGRAPHY OF ANALYTICAL METHODS FOR ALKALI METALS  

DOE Green Energy (OSTI)

A total of 107 abstracts is presented on analytical methods for alkali metals, as a part of a program for the evaluation of the performance of the primary cold trap from the Enrico Fermi Reactor. The abstracts are arranged into sections dealing with general aspects; sampling and dissolution techniques; and determination of uncombined alkali metal, oxygen, carbon, hydrogen, nitrogen, and other impurities. (D.L.C.)

Garcia, E.E.; LaMont, B.D.

1964-03-01T23:59:59.000Z

110

Fundamental Properties of Salts  

SciTech Connect

Thermal properties of molten salt systems are of interest to electrorefining operations, pertaining to both the Fuel Cycle Research & Development Program (FCR&D) and Spent Fuel Treatment Mission, currently being pursued by the Department of Energy (DOE). The phase stability of molten salts in an electrorefiner may be adversely impacted by the build-up of fission products in the electrolyte. Potential situations that need to be avoided, during electrorefining operations, include (i) fissile elements build up in the salt that might approach the criticality limits specified for the vessel, (ii) electrolyte freezing at the operating temperature of the electrorefiner due to changes in the liquidus temperature, and (iii) phase separation (non-homogenous solution). The stability (and homogeneity) of the phases can be monitored by studying the thermal characteristics of the molten salts as a function of impurity concentration. Simulated salt compositions consisting of the selected rare earth and alkaline earth chlorides, with a eutectic mixture of LiCl-KCl as the carrier electrolyte, were studied to determine the melting points (thermal characteristics) using a Differential Scanning Calorimeter (DSC). The experimental data were used to model the liquidus temperature. On the basis of the this data, it became possible to predict a spent fuel treatment processing scenario under which electrorefining could no longer be performed as a result of increasing liquidus temperatures of the electrolyte.

Toni Y Gutknecht; Guy L Fredrickson

2012-11-01T23:59:59.000Z

111

Salt Creek Student Homepage  

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

Salt Creek Investigation Salt Creek Investigation</2> "Whales Dying in the Pacific Ocean" "Fish Dying in Lake Michigan" Recent headlines remind us of environmental problems near and far away. Scientists have been wondering if these problems could be due to the warmer temperatures this past spring and summer or could there be other reasons? Lack of rain and near drought conditions have forced many areas to restrict water use. We know from past history that pollution affects our drinking water and marine life. Remember what we read about Lake Erie and from reading A River Ran Wild by Lynne Cherry. There are many factors affecting the environment around us . . . even in Salt Creek which runs through our area. We may not be able to investigate the Pacific Ocean and Lake Michigan

112

Gas releases from salt  

Science Conference Proceedings (OSTI)

The occurrence of gas in salt mines and caverns has presented some serious problems to facility operators. Salt mines have long experienced sudden, usually unexpected expulsions of gas and salt from a production face, commonly known as outbursts. Outbursts can release over one million cubic feet of methane and fractured salt, and are responsible for the lives of numerous miners and explosions. Equipment, production time, and even entire mines have been lost due to outbursts. An outburst creates a cornucopian shaped hole that can reach heights of several hundred feet. The potential occurrence of outbursts must be factored into mine design and mining methods. In caverns, the occurrence of outbursts and steady infiltration of gas into stored product can effect the quality of the product, particularly over the long-term, and in some cases renders the product unusable as is or difficult to transport. Gas has also been known to collect in the roof traps of caverns resulting in safety and operational concerns. The intent of this paper is to summarize the existing knowledge on gas releases from salt. The compiled information can provide a better understanding of the phenomena and gain insight into the causative mechanisms that, once established, can help mitigate the variety of problems associated with gas releases from salt. Outbursts, as documented in mines, are discussed first. This is followed by a discussion of the relatively slow gas infiltration into stored crude oil, as observed and modeled in the caverns of the US Strategic Petroleum Reserve. A model that predicts outburst pressure kicks in caverns is also discussed.

Ehgartner, B.; Neal, J.; Hinkebein, T.

1998-06-01T23:59:59.000Z

113

Catalytic Gasification of Coal using Eutectic Salt Mixtures  

SciTech Connect

The objectives of this study are to: identify appropriate eutectic salt mixture catalysts for coal gasification; assess agglomeration tendency of catalyzed coal; evaluate various catalyst impregnation techniques to improve initial catalyst dispersion; evaluate effects of major process variables (such as temperature, system pressure, etc.) on coal gasification; evaluate the recovery, regeneration and recycle of the spent catalysts; and conduct an analysis and modeling of the gasification process to provide better understanding of the fundamental mechanisms and kinetics of the process. A review of the collected literature was carried out. The catalysts which have been used for gasification can be roughly classified under the following five groups: alkali metal salts; alkaline earth metal oxides and salts; mineral substances or ash in coal; transition metals and their oxides and salts; and eutectic salt mixtures. Studies involving the use of gasification catalysts have been conducted. However, most of the studies focused on the application of individual catalysts. Only two publications have reported the study of gasification of coal char in CO2 and steam catalyzed by eutectic salt mixture catalysts. By using the eutectic mixtures of salts that show good activity as individual compounds, the gasification temperature can be reduced possibly with still better activity and gasification rates due to improved dispersion of the molten catalyst on the coal particles. For similar metal/carbon atomic ratios, eutectic catalysts were found to be consistently more active than their respective single salts. But the exact roles that the eutectic salt mixtures play in these are not well understood and details of the mechanisms remain unclear. The effects of the surface property of coals and the application methods of eutectic salt mixture catalysts with coal chars on the reactivity of gasification will be studied. Based on our preliminary evaluation of the literature, a ternary eutectic salt mixture consisting of Li- Na- and K- carbonates has the potential as gasification catalyst. To verify the literature reported, melting points for various compositions consisting of these three salts and the temperature range over which the mixture remained molten were determined in the lab. For mixtures with different concentrations of the three salts, the temperatures at which the mixtures were found to be in complete molten state were recorded. By increasing the amount of Li2CO3, the melting temperature range was reduced significantly. In the literature, the eutectic mixtures of Li- Na- and K-carbonates are claimed to have a lower activation energy than that of K2CO3 alone and they remain molten at a lower temperature than pure K2CO3. The slow increase in the gasification rates with eutectics reported in the literature is believed to be due to a gradual penetration of the coals and coal char particles by the molten and viscous catalyst phase. The even spreading of the salt phase seems to increase the overall carbon conversion rate. In the next reporting period, a number of eutectic salts and methods of their application on the coal will be identified and tested.

Atul Sheth; Pradeep Agrawal; Yaw D. Yeboah

1998-12-04T23:59:59.000Z

114

COAL LIQUEFACTION STUDIES USING PHOSPHORIC ACID AT MODERATE TEMPERATURES AND PRESSURES  

E-Print Network (OSTI)

lit since in their molten salt form they may show activitiesplus hydrogen. bisulfate molten salt system, thus the acidIn run 29 a molten sulfate salt system was studied. A melt

McLean, J.B.

2010-01-01T23:59:59.000Z

115

RECHARGEABLE MOLTEN-SALT CELLS  

E-Print Network (OSTI)

KC! /FeS 2 cell lithium-silicon magnesium oxide molten-saltmolten-salt cells Na/Na glass/Na:z.Sn-S cell Na/NazO•xA!Symposium on Molten Salts, Physical Electrochemistry

Cairns, Elton J.

2013-01-01T23:59:59.000Z

116

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

117

Actinide removal from spent salts  

DOE Patents (OSTI)

A method for removing actinide contaminants (uranium and thorium) 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 are added to precipitate the thorium as thorium oxide and/or the uranium as either uranium oxide or as a diuranate salt. The precipitated materials are filtered, dried and packaged for disposal as radioactive waste. About 90% of the thorium and/or uranium present is removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be 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 0.1 ppm of thorium or uranium.

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

2002-01-01T23:59:59.000Z

118

Sampling apparatus for real-time alkali monitor  

DOE Patents (OSTI)

This report describes a sampling apparatus which provides representatives samples of high-temperature, high-pressure coal- derived process gases for analysis of alkali concentrations in either a gaseous phase or in a particulate-bearing gaseous phase by a real-time alkali monitor. The apparatus includes a sampling probe in the form of a ceramic tube that is inserted in the stream of combustion products for gathering a representative stream of gaseous products. Critical flow orifices are connected in series between the probe and an alkali monitor burner. A valved vent line connected in-line between the critical flow orifices is used to vent a significant percentage of the flow from the first critical flow orifice device to maintain the upstream pressure required to provide the desired flow rate through the second critical orifice to the alkali monitor burner. The gaseous products in the system between the probe and the burner is heated to inhibit condensation of alkali species. 2 figs.

French, W.E.; Logan, R.G.; Pineault, R.L.

1989-02-27T23:59:59.000Z

119

Tuning of the Metal-Insulator Transition via Alkali Adsorption  

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

Tuning of the Metal-Insulator Tuning of the Metal-Insulator Transition via Alkali Adsorption Tuning of the Metal-Insulator Transition via Alkali Adsorption Print Wednesday, 29 March 2006 00:00 Turning a material from an insulator to a metal, or vice versa, by light irradiation, exposure to electric or magnetic fields, or applying small changes in temperature, pressure, or doping-such intriguing control of a material's electronic properties is possible by exploiting strongly interacting or "correlated" electrons. Now a team of researchers from the University of Kiel in Germany and the ALS has found a novel, surprising way to continuously transform a layered metallic transition-metal compound, TaS2, into an insulator. Using angle-resolved photoemission spectroscopy (ARPES), they have demonstrated that adsorption of alkali atoms onto this material's surface gradually makes it more insulating, although in general, alkali adsorption should lead to more metallic behavior, as alkali atoms easily give away their loosely bound outermost electron.

120

Molten salt thermal energy storage systems. Project 8981, final report  

DOE Green Energy (OSTI)

The feasibility of storing thermal energy at temperatures of 450/sup 0/ to 535/sup 0/C (850/sup 0/ to 1000/sup 0/F) in the form of latent heat of fusion has been examined for over 30 inorganic salts and salt mixtures. Alkali carbonate mixtures are attractive as phase-change storage materials in this temperature range because of their relatively high storage capacity and thermal conductivity, moderate cost, low volumetric expansion upon melting, low corrosivity, and good chemical stability. An equimolar mixture of Li/sub 2/CO/sub 3/ and K/sub 2/CO/sub 3/, which melts at 505/sup 0/C with a latent heat of 148 Btu/lb, was chosen for experimental study. The cyclic charge/discharge behavior of laboratory- and engineering-scale systems was determined and compared with predictions based on a mathematical heat-transfer model that was developed during this program. The thermal performance of one engineering-scale unit remained very stable during 1400 hours of cyclic operation. Several means of improving heat conduction through the solid salt were explored. Areas requiring further investigation have been identified.

Maru, H.C.; Dullea, J.F.; Kardas, A.; Paul, L.

1978-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Fast Pyrolysis of Poplar Using a Captive Sample Reactor: Effects of Inorganic Salts on Primary Pyrolysis Products  

SciTech Connect

We have constructed a captive sample reactor (CSR) to study fast pyrolysis of biomass. The reactor uses a stainless steel wire mesh to surround biomass materials with an isothermal environment by independent controlling of heating rates and pyrolysis temperatures. The vapors produced during pyrolysis are immediately entrained and transported in He carrier gas to a molecular beam mass spectrometer (MBMS). Formation of secondary products is minimized by rapidly quenching the sample support with liquid nitrogen. A range of alkali and alkaline earth metal (AAEM) and transition metal salts were tested to study their effect on composition of primary pyrolysis products. Multivariate curve resolution (MCR) analysis of the MBMS data shows that transition metal salts enhance pyrolysis of carbohydrates and AAEM salts enhances pyrolysis of lignin. This was supported by performing similar separate studies on cellulose, hemicellulose and extracted lignin. The effect of salts on char formation is also discussed.

Mukarakate, C.; Robichaud, D.; Donohoe, B.; Jarvis, M.; Mino, K.; Bahng, M. K.; Nimlos, M.

2012-01-01T23:59:59.000Z

122

Radiolysis of Salts and Long-Term Storage Issues for Both Pure and Impure PuO{sub 2} Materials in Plutonium Storage Containers  

SciTech Connect

The Material Identification and Surveillance (MIS) project sponsored a literature search on the effects of radiation on salts, with focus on alkali chlorides. The goal of the survey was to provide a basis for estimating the magnitude of {alpha} radiation effects on alkali chlorides that can accompany plutonium oxide (PuO{sub 2}) into storage. Chloride radiolysis can yield potentially corrosive gases in plutonium storage containers that can adversely affect long-term stability. This literature search was primarily done to provide a tutorial on this topic, especially for personnel with nonradiation chemistry backgrounds.

Lav Tandon

2000-05-01T23:59:59.000Z

123

Gabbs Alkali Flat Geothermal Area | Open Energy Information  

Open Energy Info (EERE)

Gabbs Alkali Flat Geothermal Area Gabbs Alkali Flat Geothermal Area Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Geothermal Resource Area: Gabbs Alkali Flat Geothermal Area Contents 1 Area Overview 2 History and Infrastructure 3 Regulatory and Environmental Issues 4 Exploration History 5 Well Field Description 6 Geology of the Area 7 Geofluid Geochemistry 8 NEPA-Related Analyses (0) 9 Exploration Activities (2) 10 References Area Overview Geothermal Area Profile Location: Nevada Exploration Region: Walker-Lane Transition Zone Geothermal Region GEA Development Phase: 2008 USGS Resource Estimate Mean Reservoir Temp: Estimated Reservoir Volume: Mean Capacity: Click "Edit With Form" above to add content History and Infrastructure Operating Power Plants: 0 No geothermal plants listed.

124

Salt Creek Scenario  

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

Scenario Scenario HELP Index Summary Scenario References Student Pages Two branches of Salt Creek run through the city of Rolling Meadows, Illinois, not far from our school. Five members of our team of eighth grade teachers from different subject areas (science, language arts, bilingual education and special education), decided to develop an interdisciplinary study of Salt Creek as a way of giving our students authentic experiences in environmental studies. The unit begins when students enter school in August, running through the third week of September, and resuming for three weeks in October. Extension activities based on using the data gathered at the creek continue throughout the school year, culminating in a presentation at a city council meeting in the spring.

125

Method of recovery of alkali-metal constituents from coal-conversion residues. [Patent application  

DOE Patents (OSTI)

A coal gasification operation or similar conversion process is carried out in the presence of an alkali metal-containing catalyst producing char particles containing alkali metal residues. Alkali metal constituents are recovered from the particles by burning the particles to increase their size and density and then leaching the particles of increased size and density with water, to extract the water-soluble alkali metal constituents.

Not Available

1981-04-22T23:59:59.000Z

126

Process and apparatus for obtaining silicon from fluosilicic acid  

DOE Patents (OSTI)

Process for producing low cost, high purity solar grade Si wherein a reduction reaction, preferably the reduction of SiF.sub.4, by an alkali metal (Na preferred) is carried out inside a reaction chamber. The chamber wall and bottom surfaces are configured so as to facilitate the continuous separation of the products of reaction (Si and NaF) and removal of the molten salt by discharging the salt through one or more ports at the bottom of the reaction chamber. Such process is especially useful where it is desirable to discharge the reaction salt products from the reactor and retain silicon within the chamber for later removal.

Nanis, Leonard (Palo Alto, CA); Sanjurjo, Angel (San Jose, CA)

1988-05-31T23:59:59.000Z

127

Method of assembling and sealing an alkali metal battery  

SciTech Connect

A method of initially assembling and then subsequently hermetically sealing a container portion of an alkali metal battery to a ceramic portion of such a battery is disclosed. Sealing surfaces are formed respectively on a container portion and a ceramic portion of an alkali metal battery. These sealing surfaces are brought into juxtaposition and a material is interposed therebetween. This interposed material is one which will diffuse into sealing relationship with both the container portion and the ceramic portion of the alkali metal battery at operational temperatures of such a battery. A pressure is applied between these sealing surfaces to cause the interposed material to be brought into intimate physical contact with such juxtaposed surfaces. A temporary sealing material which will provide a seal against a flow of alkali metal battery reactants therethrough at room temperatures and is applied over the juxtaposed sealing surfaces and material interposed therebetween. The entire assembly is heated to an operational temperature so that the interposed material diffuses into the container portion and the ceramic portion to form a hermetic seal therebetween. The pressure applied to the juxtaposed sealing surfaces is maintained in order to ensure the continuation of the hermetic seal.

Elkins, Perry E. (Santa Ana, CA); Bell, Jerry E. (Santa Ana, CA); Harlow, Richard A. (Newport Beach, CA); Chase, Gordon G. (San Diego, CA)

1983-01-01T23:59:59.000Z

128

High capacity nickel battery material doped with alkali metal cations  

SciTech Connect

A high capacity battery material is made, consisting essentially of hydrated Ni(II) hydroxide, and about 5 wt. % to about 40 wt. % of Ni(IV) hydrated oxide interlayer doped with alkali metal cations selected from potassium, sodium and lithium cations.

Jackovitz, John F. (Monroeville, PA); Pantier, Earl A. (Penn Hills, PA)

1982-05-18T23:59:59.000Z

129

Method of assembling and sealing an alkali metal battery  

DOE Patents (OSTI)

A method of initially assembling and then subsequently hermetically sealing a container portion of an alkali metal battery to a ceramic portion of such a battery is disclosed. Sealing surfaces are formed respectively on a container portion and a ceramic portion of an alkali metal battery. These sealing surfaces are brought into juxtaposition and a material is interposed there between. This interposed material is one which will diffuse into sealing relationship with both the container portion and the ceramic portion of the alkali metal battery at operational temperatures of such a battery. A pressure is applied between these sealing surfaces to cause the interposed material to be brought into intimate physical contact with such juxtaposed surfaces. A temporary sealing material which will provide a seal against a flow of alkali metal battery reactants there through at room temperatures and is applied over the juxtaposed sealing surfaces and material interposed there between. The entire assembly is heated to an operational temperature so that the interposed material diffuses into the container portion and the ceramic portion to form a hermetic seal there between. The pressure applied to the juxtaposed sealing surfaces is maintained in order to ensure the continuation of the hermetic seal. 4 figs.

Elkins, P.E.; Bell, J.E.; Harlow, R.A.; Chase, G.G.

1983-03-01T23:59:59.000Z

130

Molten salt lithium cells  

DOE Patents (OSTI)

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400 to 500/sup 0/C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell which may be operated at temperatures between about 100 to 170/sup 0/C. The cell is comprised of an electrolyte, which preferably includes lithium nitrate, and a lithium or lithium alloy electrode.

Raistrick, I.D.; Poris, J.; Huggins, R.A.

1980-07-18T23:59:59.000Z

131

Molten salt lithium cells  

DOE Patents (OSTI)

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400.degree.-500.degree. C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell (10) which may be operated at temperatures between about 100.degree.-170.degree. C. Cell (10) comprises an electrolyte (16), which preferably includes lithium nitrate, and a lithium or lithium alloy electrode (12).

Raistrick, Ian D. (Menlo Park, CA); Poris, Jaime (Portola Valley, CA); Huggins, Robert A. (Stanford, CA)

1983-01-01T23:59:59.000Z

132

Molten salt lithium cells  

DOE Patents (OSTI)

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400.degree.-500.degree. C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell (10) which may be operated at temperatures between about 100.degree.-170.degree. C. Cell (10) comprises an electrolyte (16), which preferably includes lithium nitrate, and a lithium or lithium alloy electrode (12).

Raistrick, Ian D. (Menlo Park, CA); Poris, Jaime (Portola Valley, CA); Huggins, Robert A. (Stanford, CA)

1982-02-09T23:59:59.000Z

133

salt lake city.cdr  

Office of Legacy Management (LM)

Locations of the Salt Lake City Processing and Disposal Sites Locations of the Salt Lake City Processing and Disposal Sites This fact sheet provides information about the Uranium Mill Tailings Radiation Control Act of 1978 Title I processing site and disposal site at Salt Lake City, Utah. These sites are managed by the U.S. Department of Energy Office of Legacy Management. Salt Lake City, Utah, Processing and Disposal Sites Site Descriptions and History Regulatory Setting The former Salt Lake City processing site is located about 4 miles south-southwest of the center of Salt Lake City, Utah, at 3300 South and Interstate 15. The Vitro Chemical Company processed uranium and vanadium ore at the site from 1951 until 1968. Milling operations conducted at the processing site created radioactive tailings, a predominantly sandy material.

134

Electrolyte salts for nonaqueous electrolytes  

Science Conference Proceedings (OSTI)

Metal complex salts may be used in lithium ion batteries. Such metal complex salts not only perform as an electrolyte salt in a lithium ion batteries with high solubility and conductivity, but also can act as redox shuttles that provide overcharge protection of individual cells in a battery pack and/or as electrolyte additives to provide other mechanisms to provide overcharge protection to lithium ion batteries. The metal complex salts have at least one aromatic ring. The aromatic moiety may be reversibly oxidized/reduced at a potential slightly higher than the working potential of the positive electrode in the lithium ion battery. The metal complex salts may also be known as overcharge protection salts.

Amine, Khalil; Zhang, Zhengcheng; Chen, Zonghai

2012-10-09T23:59:59.000Z

135

Energy densification of biomass-derived organic acids  

DOE Patents (OSTI)

A process for upgrading an organic acid includes neutralizing the organic acid to form a salt and thermally decomposing the resulting salt to form an energy densified product. In certain embodiments, the organic acid is levulinic acid. The process may further include upgrading the energy densified product by conversion to alcohol and subsequent dehydration.

Wheeler, M. Clayton

2013-01-29T23:59:59.000Z

136

Batteries using molten salt electrolyte  

SciTech Connect

An electrolyte system suitable for a molten salt electrolyte battery is described where the electrolyte system is a molten nitrate compound, an organic compound containing dissolved lithium salts, or a 1-ethyl-3-methlyimidazolium salt with a melting temperature between approximately room temperature and approximately 250.degree. C. With a compatible anode and cathode, the electrolyte system is utilized in a battery as a power source suitable for oil/gas borehole applications and in heat sensors.

Guidotti, Ronald A. (Albuquerque, NM)

2003-04-08T23:59:59.000Z

137

Electrochromic Salts, Solutions, and Devices  

DOE Patents (OSTI)

Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky, T. Mark (Los Alamos, NM)

2008-11-11T23:59:59.000Z

138

Electrochromic salts, solutions, and devices  

DOE Patents (OSTI)

Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky,7,064,212 T. Mark (Los Alamos, NM)

2006-06-20T23:59:59.000Z

139

Electrochromic Salts, Solutions, and Devices  

DOE Patents (OSTI)

Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky, T. Mark (Los Alamos, NM)

2008-10-14T23:59:59.000Z

140

Molten Salts, Magnesium and Aluminum  

Science Conference Proceedings (OSTI)

Mar 1, 2011 ... Chloride 2011: Practice and Theory of Chloride-Based Metallurgy: Molten Salts, Magnesium and Aluminum Sponsored by: The Minerals, ...

Note: This page contains sample records for the topic "acids alkalies salts" 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

Process for carbonaceous material conversion and recovery of alkali metal catalyst constituents held by ion exchange sites in conversion residue  

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 for the particles by contacting or washing them with an aqueous solution containing calcium or magnesium ions in an alkali metal recovery zone at a low temperature, preferably below about 249.degree. F. During the washing or leaching process, the calcium or magnesium ions displace alkali metal ions held by ion exchange sites in the particles thereby liberating the ions and producing an aqueous effluent containing alkali metal constituents. The aqueous effluent from the alkali metal recovery zone is then recycled to the conversion process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst.

Sharp, David W. (Seabrook, TX)

1980-01-01T23:59:59.000Z

142

A Study on Biogas from Anaerobic Digestion with the Distiller's Grains via Lactic Acid Fermentation  

Science Conference Proceedings (OSTI)

The methane production of the distiller’s grains via lactic acid fermentation (shorter for the fermentation residue) was investigated, and the variable trend of pH values, alkali concentration and volatile fatty acids were examined. The results ... Keywords: the residue of distillers' grains via lactic acid fermentation, biomass wastes, anaerobic digestion, volatile fatty acids, biogas production

Li-Hong Wang; Wang Qunhui; Sun Xiaohong; Xin Zhao

2010-12-01T23:59:59.000Z

143

Molten Metal Treatment by Salt Fluxing with Low Environmental Emissions  

SciTech Connect

Abstract: Chlorine gas is traditionally used for fluxing of aluminum melt for removal of alkali and alkaline earth elements. However this results in undesirable emissions of particulate matter and gases such as HCl and chlorine, which are often at unacceptable levels. Additionally, chlorine gas is highly toxic and its handling, storage, and use pose risks to employees and the local community. Holding of even minimal amounts of chlorine necessitates extensive training for all plant employees. Fugitive emissions from chlorine usage within the plant cause accelerated corrosion of plant equipment. The Secondary Aluminum Maximum Achievable Control Technology (MACT) under the Clean Air Act, finalized in March 2000 has set very tough new limits on particulate matter (PM) and total hydrogen chloride emissions from aluminum melting and holding furnaces. These limits are 0.4 and 0.1 lbs per ton of aluminum for hydrogen chloride and particulate emissions, respectively. Assuming new technologies for meeting these limits can be found, additional requirements under the Clean Air Act (Prevention of Significant Deterioration and New Source Review) trigger Best Available Control Technology (BACT) for new sources with annual emissions (net emissions not expressed per ton of production) over specified amounts. BACT currently is lime coated bag-houses for control of particulate and HCl emissions. These controls are expensive, difficult to operate and maintain, and result in reduced American competitiveness in the global economy. Solid salt fluxing is emerging as a viable option for the replacement of chlorine gas fluxing, provided emissions can be consistently maintained below the required levels. This project was a cooperative effort between the Ohio State University and Alcoa to investigate and optimize the effects of solid chloride flux addition in molten metal for alkali impurity and non-metallic inclusion removal minimizing dust and toxic emissions and maximizing energy conservation. In this program, the salt metal interactions were studies and the emissions at laboratory scale at OSU were monitored. The goal of the project was to obtain a fundamental understanding, based on first principles, of the pollutant formation that occurs when the salts are used in furnaces. This information will be used to control process parameters so that emissions are consistently below the required levels. The information obtained in these experiments will be used in industrial furnaces at aluminum plants and which will help in optimizing the process.

Yogeshwar Sahai

2007-07-31T23:59:59.000Z

144

SALT-ANL. Systems Analysis Process Simulation  

Science Conference Proceedings (OSTI)

SALT (Systems Analysis Language Translator), a systems- analysis and process-simulation program for steady-state and dynamic systems, can also be used for optimization and sensitivity studies. SALT employs state-of-the-art numerical techniques including a hybrid steepest-descent/quasi-Newtonian multidimensional nonlinear equation solver, sequential quadratic programming methods for optimization, and multistep integration methods for both stiff and nonstiff systems of differential equations. Based on a preprocessor concept where a `new` system driver can be written for each application, SALT-ANL contains precompiled component models, several flow types, and a number of thermodynamic and transport property routines, including a gas chemical-equilibrium code. It has been applied to the study of open-cycle and liquid-metal magnetohydrodynamic systems, fuel cells, ocean thermal energy conversion, municipal solid-waste processing, fusion, breeder reactors, and geothermal and solar-energy systems. Models available include: combustor, compressor, deaerator, gas-diffuser, fuel-dryer, feedwater-heater, flash-tank, gas-turbine, heater, heat-exchanger, flow-initiator, fuel-flow-initiator, molten-carbonate fuel-cell, liquid-metal diffuser, magnetohydrodynamic-generator, liquid-metal magnetohydrodynamic-generator, liquid-metal nozzle, liquid-metal pipe, flow-mixer, gas-nozzle, phosphoric acid fuel-cell, pump, pipe-calculator, steam-condenser, steam-drum, liquid-gas separator, stack, solid-oxide fuel-cell, flow-splitter, steam-turbine, two-phase diffuser, two-phase mixer, and two-phase nozzle. Input data to the SALT program describe the system configuration for the specific problem to be analyzed and provide instructions defining system constraints, objective functions, parameter sweeps, etc. to generate a PL/I program representing the system problem and performing the various analytic tasks.

Berry, G.F.; Geyer, H.K. [Argonne National Lab., IL (United States)

1992-02-26T23:59:59.000Z

145

Developments in Molten Salt and Liquid-Salt-Cooled Reactors  

Science Conference Proceedings (OSTI)

In the last 5 years, there has been a rapid growth in interest in the use of high-temperature (700 to 1000 deg C) molten and liquid fluoride salts as coolants in nuclear systems. This renewed interest is a consequence of new applications for high-temperature heat and the development of new reactor concepts. Fluoride salts have melting points between 350 and 500 deg C; thus, they are of use only in high-temperature systems. Historically, steam cycles with temperature limits of {approx}550 deg C have been the only efficient method to convert heat to electricity. This limitation produced few incentives to develop high-temperature reactors for electricity production. However, recent advances in Brayton gas turbine technology now make it possible to convert higher-temperature heat efficiency into electricity on an industrial scale and thus have created the enabling technology for more efficient nuclear reactors. Simultaneously, there is a growing interest in using high-temperature nuclear heat for the production of hydrogen and shale oil. Five nuclear-related applications are being investigated: (1) liquid-salt heat-transport systems in hydrogen and shale oil production systems; (2) the advanced high-temperature reactor, which uses a graphite-matrix coated-particle fuel and a liquid salt coolant; (3) the liquid-salt-cooled fast reactor which uses metal-clad fuel and a liquid salt coolant; (4) the molten salt reactor, with the fuel dissolved in the molten salt coolant; and (5) fusion energy systems. The reasons for the new interest in liquid salt coolants, the reactor concepts, and the relevant programs are described. (author)

Forsberg, Charles W. [Oak Ridge National Laboratory, P.O. Box 2008, Oak Ridge, TN 37831-6165 (United States)

2006-07-01T23:59:59.000Z

146

CANMET/Industry Research Consortium on Alkali-Aggregate Reactivity  

Science Conference Proceedings (OSTI)

The alkali-silica reaction (ASR) is a deleterious chemical reaction that can result in the deterioration of concrete structures. This report presents the results of an R&D study, funded by a broadly-based multi-national industry consortium, that is developing an engineering data base on the long-term effectiveness of fly ash and other supplementary cementing materials (SCMs) in counteracting ASR in concrete.

1997-12-23T23:59:59.000Z

147

Extracting information from the molten salt database  

Science Conference Proceedings (OSTI)

Molten salt technology is a catchall phrase that includes some very diverse ... nologies are linked by the general characteristics of molten salts that can function

148

Oxygen-Consuming Chlor-Alkali Cell Configured To Minimize Peroxide  

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

Oxygen-Consuming Chlor-Alkali Cell Oxygen-Consuming Chlor-Alkali Cell Oxygen-Consuming Chlor-Alkali Cell Configured To Minimize Peroxide Formation Oxygen-consuming zero gap chlor-alkali cell was configured to minimize peroxide formation. Available for thumbnail of Feynman Center (505) 665-9090 Email Oxygen-Consuming Chlor-Alkali Cell Configured To Minimize Peroxide Formation Oxygen-consuming zero gap chlor-alkali cell was configured to minimize peroxide formation. The cell included an ion-exchange membrane that divided the cell into an anode chamber including an anode and a cathode chamber including an oxygen gas diffusion cathode. The cathode included a single-piece of electrically conducting graphitized carbon cloth. Catalyst and polytetrafluoroethylene were attached to only one side of the cloth.

149

Nucleic acids encoding metal uptake transporters and their uses  

DOE Patents (OSTI)

The invention provides LCT1 nucleic acids which encode metal ion uptake transporters. The invention also provides methods of modulating heavy metal and alkali metal uptake in plants. The methods involve producing transgenic plants comprising a recombinant expression cassette containing an LCT1 nucleic acid linked to a plant promoter.

Schroeder, Julian I. (La Jolla, CA); Antosiewicz, Danuta M. (Warsaw, PL); Schachtman, Daniel P. (Tranmere, AU); Clemens, Stephan (San Diego, CA)

1999-01-01T23:59:59.000Z

150

PRODUCTION OF TRIFLUOROACETIC ACID COMPOUNDS  

DOE Patents (OSTI)

A process is described for the preparation of trifluoroacetic acid. Acetone vapor diluted wlth nitrogen and fluorine also diluted with nltrogen are fed separately at a temperature of about 210 deg C into a reaction vessel containing a catalyst mass selected from-the group consisting of silver and gold. The temperature in the reaction vessel is maintained in the range of 200 deg to 250 deg C. The reaction product, trifluoroacetyl fluoride, is absorbed in aqueous alkali solution. Trifluoroacetic acid is recovered from the solution by acidification wlth an acid such as sulfuric followed by steam distillation.

Haworth, W.N.; Stacey, M.

1949-08-30T23:59:59.000Z

151

Novel Ternary Molten Salt Electrolytes for intermediate-temperature sodium/nickel chloride batteries  

SciTech Connect

The sodium-nickel chloride (ZEBRA) battery is typically operated at relatively high temperature (250~350°C) to achieve adequate electrochemical performance. Reducing the operating temperature in the range of 150 to 200°C can lead to enhanced cycle life by suppressing temperature related degradation mechanisms. The reduced temperature range also allows for lower cost materials of construction such as elastomeric sealants and gaskets. To achieve adequate electrochemical performance at lower operating temperatures requires an overall reduction in ohmic losses associated with temperature. This includes reducing the ohmic resistance of ?”-alumina solid electrolyte (BASE) and the incorporation of low melting point molten salt as the secondary electrolyte. In present work, planar-type Na/NiCl2 cells with a thin flat plate BASE (600 ?m) and low melting point secondary electrolyte were evaluated at reduced temperatures. Molten salt formulation for use as secondary electrolytes were fabricated by the partial replace of NaCl in the standard secondary electrolyte (NaAlCl4) with other lower melting point alkali metal salts such as NaBr, LiCl, and LiBr. Electrochemical characterization of the ternary molten salts demonstrated , improved ionic conductivity, and sufficient electrochemical window at reduced temperatures. Furthermore, Na/NiCl2 cells with 50 mol% NaBr-containing secondary electrolyte exhibited reduced polarizations at 175°C compared to the cell with the standard NaAlCl4 catholyte. The cells also exhibited stable cycling performance even at 150oC.

Li, Guosheng; Lu, Xiaochuan; Coyle, Christopher A.; Kim, Jin Yong; Lemmon, John P.; Sprenkle, Vincent L.; Yang, Zhenguo

2012-12-15T23:59:59.000Z

152

Modeling Solute Thermokinetics in LiCI-KCI Molten Salt for Nuclear Waste Separation  

SciTech Connect

Recovery of actinides is an integral part of a closed nuclear fuel cycle. Pyrometallurgical nuclear fuel recycling processes have been developed in the past for recovering actinides from spent metallic and nitride fuels. The process is essentially to dissolve the spent fuel in a molten salt and then extract just the actinides for reuse in a reactor. Extraction is typically done through electrorefining, which involves electrochemical reduction of the dissolved actinides and plating onto a cathode. Knowledge of a number of basic thermokinetic properties of salts and salt-fuel mixtures is necessary for optimizing present and developing new approaches for pyrometallurgical waste processing. The properties of salt-fuel mixtures are presently being studied, but there are so many solutes and varying concentrations that direct experimental investigation is prohibitively time consuming and expensive (particularly for radioactive elements like Pu). Therefore, there is a need to reduce the number of required experiments through modeling of salt and salt-fuel mixture properties. This project will develop first-principles-based molecular modeling and simulation approaches to predict fundamental thermokinetic properties of dissolved actinides and fission products in molten salts. The focus of the proposed work is on property changes with higher concentrations (up to 5 mol%) of dissolved fuel components, where there is still very limited experimental data. The properties predicted with the modeling will be density, which is used to assess the amount of dissolved material in the salt; diffusion coefficients, which can control rates of material transport during separation; and solute activity, which determines total solubility and reduction potentials used during electrorefining. The work will focus on La, Sr, and U, which are chosen to include the important distinct categories of lanthanides, alkali earths, and actinides, respectively. Studies will be performed using LiCl-KCl salt at the eutectic composition (58 mol% LiCl, 42 mol% KCl), which is used for treating spent EBR-II fuel. The same process being used for EBRII fuel is currently being studied for widespread international implementation. The methods will focus on first-principles and first- principles derived interatomic potential based simulations, primarily using molecular dynamics. Results will be validated against existing literature and parallel ongoing experimental efforts. The simulation results will be of value for interpreting experimental results, validating analytical models, and for optimizing waste separation by potentially developing new salt configurations and operating conditions.

Morgan, Dane; Eapen, Jacob

2013-10-01T23:59:59.000Z

153

Alkali compounds catalyzed low temperature methanol synthesis over Cu-based catalyst  

Science Conference Proceedings (OSTI)

A novel mixed catalyst system containing alkali compounds over Cu/MgO-Na catalyst was developed to synthesize methanol from syngas via ethyl formate in a slurry reactor. The results exhibited that among the used alkali formates (HCOOM, M=Li, Na, Cs, ... Keywords: CuMgO-Na/HCOONa/catalysis system, low temperature methanol synthesis, slurry phase

Baoshan Hu

2007-12-01T23:59:59.000Z

154

Freshwater fish in salt water  

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

Freshwater fish in salt water Freshwater fish in salt water Name: Shannon Location: N/A Country: N/A Date: N/A Question: What would actually happen if a fresh water fish had to live in salt water? Replies: For most fish, they would die. But some, like eels and salmon, can move freely between the two at certain stages of their lives. To do this they have special mechanisms of excretion and absorption of salt and water. --ProfBill If you put a freshwater fish into saltwater, most fish would lose weight (from losing water from its body) and eventually die. Approximately 2% of all 21000 species of fish actually move from freshwater to saltwater or from salt to fresh at some point in their lives, the move would kill any other fish. But even with these special varieties of fish, the move must be gradual so their bodies can adjust, or they too, will die from the change. If you want to learn more about why the freshwater fish will lose water, (or why a saltwater fish in freshwater would gain water), look up the words "diffusion" and "osmosis"

155

Fracture and Healing of Rock Salt Related to Salt Caverns  

Science Conference Proceedings (OSTI)

In recent years, serious investigations of potential extension of the useful life of older caverns or of the use of abandoned caverns for waste disposal have been of interest to the technical community. All of the potential applications depend upon understanding the reamer in which older caverns and sealing systems can fail. Such an understanding will require a more detailed knowledge of the fracture of salt than has been necessary to date. Fortunately, the knowledge of the fracture and healing of salt has made significant advances in the last decade, and is in a position to yield meaningful insights to older cavern behavior. In particular, micromechanical mechanisms of fracture and the concept of a fracture mechanism map have been essential guides, as has the utilization of continuum damage mechanics. The Multimechanism Deformation Coupled Fracture (MDCF) model, which is summarized extensively in this work was developed specifically to treat both the creep and fracture of salt, and was later extended to incorporate the fracture healing process known to occur in rock salt. Fracture in salt is based on the formation and evolution of microfractures, which may take the form of wing tip cracks, either in the body or the boundary of the grain. This type of crack deforms under shear to produce a strain, and furthermore, the opening of the wing cracks produce volume strain or dilatancy. In the presence of a confining pressure, microcrack formation may be suppressed, as is often the case for triaxial compression tests or natural underground stress situations. However, if the confining pressure is insufficient to suppress fracture, then the fractures will evolve with time to give the characteristic tertiary creep response. Two first order kinetics processes, closure of cracks and healing of cracks, control the healing process. Significantly, volume strain produced by microfractures may lead to changes in the permeability of the salt, which can become a major concern in cavern sealing and operation. The MDCF model is used in three simulations of field experiments in which indirect measures were obtained of the generation of damage. The results of the simulations help to verify the model and suggest that the model captures the correct fracture behavior of rock salt. The model is used in this work to estimate the generation and location of damage around a cylindrical storage cavern. The results are interesting because stress conditions around the cylindrical cavern do not lead to large amounts of damage. Moreover, the damage is such that general failure can not readily occur, nor does the extent of the damage suggest possible increased permeation when the surrounding salt is impermeable.

Chan, K.S.; Fossum, A.F.; Munson, D.E.

1999-03-01T23:59:59.000Z

156

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

SciTech Connect

This is the progress report for the DOE grant DE-FG26-97FT97263 entitled, ''Catalytic Gasification of Coal Using Eutectic Salt Mixtures'' for the period April 1999 to October 1999. The project is being conducted jointly by Clark Atlanta University, the University of Tennessee Space Institute and Georgia Institute of Technology. The overall objectives of the project are to identify appropriate eutectic salt mixture catalysts for coal gasification; assess agglomeration tendency of catalyzed coal; evaluate various catalyst impregnation techniques to improve initial catalyst dispersion; evaluate effects of major process variables (such as temperature and system pressure) on coal gasification; evaluate the recovery, regeneration and recycle of the spent catalysts; and conduct thorough analysis and modeling of the gasification process to provide better understanding of the fundamental mechanisms and kinetics of the process. During this reporting period, free swelling index measurements of the coal, fixed-bed gasification experiments, kinetic modeling of the catalyzed gasification, and X-ray diffraction analysis of catalyst and gasified char samples were undertaken. The gasification experiments were carried out using two different eutectic salt mixtures of Li{sub 2}CO{sub 3}-Na{sub 2}CO{sub 3}-K{sub 2}CO{sub 3} (LNK) system and Na{sub 2}CO{sub 3}-K{sub 2}CO{sub 3} (NK) system. The gasification process followed a Langmuir-Hinshelwood type model. At 10 wt% of catalyst loading, the activation energy of the ternary catalyst system (LNK) was about half (98kJ/mol) the activation energy of the single catalyst system (K{sub 2}CO{sub 3}), which is about 170 kJ/ mole. The binary catalyst system (NK) showed activation energy of about 201 kJ/mol, which is slightly higher, compared to the K{sub 2}CO{sub 3} catalyst system. The ternary catalyst system was a much better eutectic catalyst system compared to the binary or single catalyst system. In general, a eutectic with a melting point less than the gasification temperature is a better substitute to the single alkali metal salts because they have good catalyst distribution and dispersion in the carbon matrix. The free selling index of the coal was about 1.5 (1 to 2) in comparison to 2.5 (2 to 3) for the coal samples with ternary eutectic. The results for the raw coal were consistent with those from the Penn State Coal Bank. The XRD characterization showed unidentified peaks in the spectra of some of the samples and require further studies to draw any conclusions at the point.

NONE

1999-10-01T23:59:59.000Z

157

Why Sequence Great Salt Lake?  

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

Great Salt Lake? Great Salt Lake? On average, the Great Salt Lake is four times saltier than the ocean and also has heavy metals, high concentrations of sulfur and petroleum seeps. In spite of all this, the lake is the saltiest body of water to support life. The lake hosts brine shrimp, algae and a diverse array of microbes, not to mention the roughly 5 million birds that migrate there annually. The secret to these microbes' ability to survive under such harsh conditions might be revealed in their genes. Researchers expect the genetic data will provide insight into how the microorganisms tolerate pollutants such as sulfur and detoxify pollutants such as sulfur and heavy metals like mercury. The information could then be used to develop bioremediation techniques. Researchers also expect that sequencing microorganisms sampled

158

Salt Lake Community College | .EDUconnections  

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

SLCC Partners with DOE's Rocky Mountain Solar Training Program This program is a joint partnership between DOE's Solar Energy Technogies Program, Salt Lake Community College, Solar Energy International, and the Utah Solar Energy Association that works to accelerate use of solar electric technologies, training and facilities at community and technical college solar training programs within a 15 western United States region. DOE Solar Instructor Training Network Salt Lake City, Utah DOE Applauds SLCC's Science and Technical Programs Architectural Technology Biology Biotechnology Biomanufacturing Chemistry Computer Science Electric Sector Training Energy Management Engineering Geographic Information Sciences Geosciences InnovaBio Manufacturing & Mechanical Engineering Technology

159

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

Science Conference Proceedings (OSTI)

The Gas Research Institute (GRI) estimates that by the year 2010, 40% or more of U.S. gas supply will be provided by supplements including substitute natural gas (SNG) from coal. These supplements must be cost competitive with other energy sources. The first generation technologies for coal gasification e.g. the Lurgi Pressure Gasification Process and the relatively newer technologies e.g. the KBW (Westinghouse) Ash Agglomerating Fluidized-Bed, U-Gas Ash Agglomerating Fluidized-Bed, British Gas Corporation/Lurgi Slagging Gasifier, Texaco Moving-Bed Gasifier, and Dow and Shell Gasification Processes, have several disadvantages. These disadvantages include high severities of gasification conditions, low methane production, high oxygen consumption, inability to handle caking coals, and unattractive economics. Another problem encountered in catalytic coal gasification is deactivation of hydroxide forms of alkali and alkaline earth metal catalysts by oxides of carbon (CO{sub x}). To seek solutions to these problems, a team consisting of Clark Atlanta University (CAU, a Historically Black College and University, HBCU), the University of Tennessee Space Institute (UTSI) and Georgia Institute of Technology (Georgia Tech) proposed to identify suitable low melting eutectic salt mixtures for improved coal gasification. The research objectives of this project were to: Identify appropriate eutectic salt mixture catalysts for coal gasification; Assess agglomeration tendency of catalyzed coal; Evaluate various catalyst impregnation techniques to improve initial catalyst dispersion; Determine catalyst dispersion at high carbon conversion levels; Evaluate effects of major process variables (such as temperature, system pressure, etc.) on coal gasification; Evaluate the recovery, regeneration and recycle of the spent catalysts; and Conduct an analysis and modeling of the gasification process to provide better understanding of the fundamental mechanisms and kinetics of the process.

Dr. Yaw D. Yeboah; Dr. Yong Xu; Dr. Atul Sheth; Dr. Pradeep Agrawal

2001-12-01T23:59:59.000Z

160

Cathode for molten salt batteries  

DOE Patents (OSTI)

A molten salt electrochemical system for battery applications comprises tetravalent sulfur as the active cathode material with a molten chloroaluminate solvent comprising a mixture of AlCl.sub.3 and MCl having a molar ratio of AlCl.sub.3 /MCl from greater than 50.0/50.0 to 80/20.

Mamantov, Gleb (Knoxville, TN); Marassi, Roberto (Camerino, IT)

1977-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Cleanup of plutonium oxide reduction black salts  

Science Conference Proceedings (OSTI)

This work describes pyrochemical processes employed to convert direc oxide reduction (DOR) black salts into discardable white salt and plutonium metal. The DOR process utilizes calcium metal as the reductant in a molten calcium chloride solvent salt to convert plutonium oxide to plutonium metal. An insoluble plutonium-rich dispersion called black salt sometimes forms between the metal phase and the salt phase. Black salts accumulated for processing were treated by one of two methods. One method utilized a scrub alloy of 70 wt % magnesium/30 wt % zinc. The other method utilized a pool of plutonium metal to agglomerate the metal phase. The two processes were similar in that calcium metal reductant and calcium chloride solvent salt were used in both cases. Four runs were performed by each method, and each method produced greater than 93% conversion of the black salt.

Giebel, R.E.; Wing, R.O.

1986-12-17T23:59:59.000Z

162

Dysprosium Extraction Using Molten Salt Electrolysis Process  

Science Conference Proceedings (OSTI)

AlCl3 was used as a chlorinating agent in order to enable an efficient dissolution of metal in the molten salt phase in the salt bath. The metal chloride which is ...

163

Improved Recovery Boiler Performance Through Control of Combustion, Sulfur, and Alkali Chemistry  

Science Conference Proceedings (OSTI)

This project involved the following objectives: 1. Determine black liquor drying and devolatilization elemental and total mass release rates and yields. 2. Develop a public domain physical/chemical kinetic model of black liquor drop combustion, including new information on drying and devolatilization. 3. Determine mechanisms and rates of sulfur scavenging in recover boilers. 4. Develop non-ideal, public-domain thermochemistry models for alkali salts appropriate for recovery boilers 5. Develop data and a one-dimensional model of a char bed in a recovery boiler. 6. Implement all of the above in comprehensive combustion code and validate effects on boiler performance. 7. Perform gasification modeling in support of INEL and commercial customers. The major accomplishments of this project corresponding to these objectives are as follows: 1. Original data for black liquor and biomass data demonstrate dependencies of particle reactions on particle size, liquor type, gas temperature, and gas composition. A comprehensive particle submodel and corresponding data developed during this project predicts particle drying (including both free and chemisorbed moisture), devolatilization, heterogeneous char oxidation, char-smelt reactions, and smelt oxidation. Data and model predictions agree, without adjustment of parameters, within their respective errors. The work performed under these tasks substantially exceeded the original objectives. 2. A separate model for sulfur scavenging and fume formation in a recovery boiler demonstrated strong dependence on both in-boiler mixing and chemistry. In particular, accurate fume particle size predictions, as determined from both laboratory and field measurements, depend on gas mixing effects in the boilers that lead to substantial particle agglomeration. Sulfur scavenging was quantitatively predicted while particle size required one empirical mixing factor to match data. 3. Condensed-phase thermochemistry algorithms were developed for salt mixtures and compared with sodium-based binary and higher order systems. Predictions and measurements were demonstrated for both salt systems and for some more complex silicate-bearing systems, substantially exceeding the original scope of this work. 4. A multi-dimensional model of char bed reactivity developed under this project demonstrated that essentially all reactions in char beds occur on or near the surface, with the internal portions of the bed being essentially inert. The model predicted composition, temperature, and velocity profiles in the bed and showed that air jet penetration is limited to the immediate vicinity of the char bed, with minimal impact on most of the bed. The modeling efforts substantially exceeded the original scope of this project. 5. Near the completion of this project, DOE withdrew the BYU portion of a multiparty agreement to complete this and additional work with no advanced warning, which compromised the integration of all of this material into a commercial computer code. However, substantial computer simulations of much of this work were initiated, but not completed. 6. The gasification modeling is nearly completed but was aborted near its completion according to a DOE redirection of funds. This affected both this and the previous tasks.

Baxter, Larry L.

2008-06-09T23:59:59.000Z

164

Waste Isolation Pilot Plant's Excavated Salt Agreement Supports...  

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

Plant's Excavated Salt Agreement Supports Conservation Education, Other Public Initiatives Waste Isolation Pilot Plant's Excavated Salt Agreement Supports Conservation Education,...

165

2-M Probe At Gabbs Alkali Flat Area (Kratt, Et Al., 2008) | Open Energy  

Open Energy Info (EERE)

2-M Probe At Gabbs Alkali Flat Area (Kratt, Et Al., 2008) 2-M Probe At Gabbs Alkali Flat Area (Kratt, Et Al., 2008) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: 2-M Probe At Gabbs Alkali Flat Area (Kratt, Et Al., 2008) Exploration Activity Details Location Gabbs Alkali Flat Area Exploration Technique 2-M Probe Activity Date Usefulness useful DOE-funding Unknown Notes More than 100 2-meter-deep temperature measurements were made during two separate surveys that took place in December 2007 and April 2008 (Figure 5). The area covered was 16 km in length parallel to the range front and a maximum of nearly 5 km out into the valley. The highest recorded temperature of 37°C was obtained approximately 100 m upslope from Rawhide hot springs. Near these springs, temperatures rapidly cool towards the

166

Investigation of the nature of electronic states in the alkali_metal oxides  

Science Conference Proceedings (OSTI)

Hartree-Fock and Density functional theories have been applied to investigate the density of electronic states and electronic band structures. We studied: oxides, peroxides, nadoxides and ozonides, alkali-metal oxides M2O, peroxides M2O2, ...

O. O. Obolonskaya

2010-05-01T23:59:59.000Z

167

Laboratory investigation of combination of alkali/surfactant/polymer technology for Daqing EOR  

Science Conference Proceedings (OSTI)

Alkali/surfactant/polymer (ASP) formulas were developed for the Daqing oil field, Peoples Republic of China, with two surfactants from the US (Petrostep B-100 and a blend of TRS-18 and TRS-40) and one Chinese surfactant (PS-D{sub 2}). Each ASP solution gave interfacial tension (IFT) values in the range of 1 {times} 10{sup {minus}3} mN/m. Rheologic studies with polyacrylamide polymers indicate that solution viscosity decreases with alkali addition, as does the pseudoplasticity of the solution. Addition of surfactant to the alkali/polymer solution increases the solution viscosity with no slope change in the viscosity-vs.-shear-rate plot. Incremental oil recovery was higher than that with waterflood; 20% original oil in place (OOIP) for 0.2-PV ASP injection and 33% OOIP for 0.3-PV ASP injection in Daqing core. Surfactant and alkali retention were both flood in the Daqing oil field.

Gao Shutang; Li Huabin; Li Hongfu [Inst. of Petroleum Exploration and Development, Daqing (China)

1995-08-01T23:59:59.000Z

168

Process and apparatus for obtaining silicon from fluosilicic acid  

DOE Patents (OSTI)

An apparatus for producing low cost, high purity solar grade Si wherein a reduction reaction, preferably the reduction of SiF.sub.4, by an alkali metal (Na preferred) is carried out inside a reaction chamber. The chamber wall and bottom surfaces are formed of graphite and configured with drainage channels so as to facilitate the continuous separation of the products of reaction (Si and NaF) and removal of the molten salt by discharging the salt through one or more ports at the bottom of the reaction chamber. Such process is especially useful where it is desirable to discharge the reaction salt products from the reactor and retain silicon within the chamber for later removal.

Nanis, Leonard (Palo Alto, CA); Sanjurjo, Angel (San Jose, CA)

1986-04-22T23:59:59.000Z

169

BLENDING ANALYSIS FOR RADIOACTIVE SALT WASTE PROCESSING FACILITY  

SciTech Connect

Savannah River National Laboratory (SRNL) evaluated methods to mix and blend the contents of the blend tanks to ensure the contents are properly blended before they are transferred from the blend tank such as Tank 21 and Tank 24 to the Salt Waste Processing Facility (SWPF) feed tank. The tank contents consist of three forms: dissolved salt solution, other waste salt solutions, and sludge containing settled solids. This paper focuses on developing the computational model and estimating the operation time of submersible slurry pump when the tank contents are adequately blended prior to their transfer to the SWPF facility. A three-dimensional computational fluid dynamics approach was taken by using the full scale configuration of SRS Type-IV tank, Tank 21H. Major solid obstructions such as the tank wall boundary, the transfer pump column, and three slurry pump housings including one active and two inactive pumps were included in the mixing performance model. Basic flow pattern results predicted by the computational model were benchmarked against the SRNL test results and literature data. Tank 21 is a waste tank that is used to prepare batches of salt feed for SWPF. The salt feed must be a homogeneous solution satisfying the acceptance criterion of the solids entrainment during transfer operation. The work scope described here consists of two modeling areas. They are the steady state flow pattern calculations before the addition of acid solution for tank blending operation and the transient mixing analysis during miscible liquid blending operation. The transient blending calculations were performed by using the 95% homogeneity criterion for the entire liquid domain of the tank. The initial conditions for the entire modeling domain were based on the steady-state flow pattern results with zero second phase concentration. The performance model was also benchmarked against the SRNL test results and literature data.

Lee, S.

2012-05-10T23:59:59.000Z

170

Preconceptual design of a salt splitting process using ceramic membranes  

SciTech Connect

Inorganic ceramic membranes for salt splitting of radioactively contaminated sodium salt solutions are being developed for treating U. S. Department of Energy tank wastes. The process consists of electrochemical separation of sodium ions from the salt solution using sodium (Na) Super Ion Conductors (NaSICON) membranes. The primary NaSICON compositions being investigated are based on rare- earth ions (RE-NaSICON). Potential applications include: caustic recycling for sludge leaching, regenerating ion exchange resins, inhibiting corrosion in carbon-steel tanks, or retrieving tank wastes; reducing the volume of low-level wastes volume to be disposed of; adjusting pH and reducing competing cations to enhance cesium ion exchange processes; reducing sodium in high-level-waste sludges; and removing sodium from acidic wastes to facilitate calcining. These applications encompass wastes stored at the Hanford, Savannah River, and Idaho National Engineering Laboratory sites. The overall project objective is to supply a salt splitting process unit that impacts the waste treatment and disposal flowsheets and meets user requirements. The potential flowsheet impacts include improving the efficiency of the waste pretreatment processes, reducing volume, and increasing the quality of the final waste disposal forms. Meeting user requirements implies developing the technology to the point where it is available as standard equipment with predictable and reliable performance. This report presents two preconceptual designs for a full-scale salt splitting process based on the RE-NaSICON membranes to distinguish critical items for testing and to provide a vision that site users can evaluate.

Kurath, D.E.; Brooks, K.P.; Hollenberg, G.W.; Clemmer, R. [Pacific Northwest National Lab., Richland, WA (United States); Balagopal, S.; Landro, T.; Sutija, D.P. [Ceramatec, Inc., Salt Lake City, UT (United States)

1997-01-01T23:59:59.000Z

171

Barium oxide, calcium oxide, magnesia, and alkali oxide free glass  

DOE Patents (OSTI)

A glass composition consisting essentially of about 10-45 mole percent of SrO; about 35-75 mole percent SiO.sub.2; one or more compounds from the group of compounds consisting of La.sub.2O.sub.3, Al.sub.2O.sub.3, B.sub.2O.sub.3, and Ni; the La.sub.2O.sub.3 less than about 20 mole percent; the Al.sub.2O.sub.3 less than about 25 mole percent; the B.sub.2O.sub.3 less than about 15 mole percent; and the Ni less than about 5 mole percent. Preferably, the glass is substantially free of barium oxide, calcium oxide, magnesia, and alkali oxide. Preferably, the glass is used as a seal in a solid oxide fuel/electrolyzer cell (SOFC) stack. The SOFC stack comprises a plurality of SOFCs connected by one or more interconnect and manifold materials and sealed by the glass. Preferably, each SOFC comprises an anode, a cathode, and a solid electrolyte.

Lu, Peizhen Kathy; Mahapatra, Manoj Kumar

2013-09-24T23:59:59.000Z

172

Quantum magnetism with polar alkali-metal dimers  

Science Conference Proceedings (OSTI)

We show that dipolar interactions between ultracold polar alkali-metal dimers in optical lattices can be used to realize a highly tunable generalization of the t-J model, which we refer to as the t-J-V-W model. The model features long-range spin-spin interactions J{sub z} and J{sub perpendicular} of XXZ type, long-range density-density interaction V, and long-range density-spin interaction W, all of which can be controlled in both magnitude and sign independently of each other and of the tunneling t. The spin's is encoded in the rotational degree of freedom of the molecules, while the interactions are controlled by applied static electric and continuous-wave microwave fields. Furthermore, we show that nuclear spins of the molecules can be used to implement an additional (orbital) degree of freedom that is coupled to the original rotational degree of freedom in a tunable way. The presented system is expected to exhibit exotic physics and to provide insights into strongly correlated phenomena in condensed-matter systems. Realistic experimental imperfections are discussed.

Gorshkov, Alexey V. [Institute for Quantum Information, California Institute of Technology, Pasadena, California 91125 (United States); Kavli Institute for Theoretical Physics, University of California, Santa Barbara, California 93106 (United States); Manmana, Salvatore R.; Chen Gang [JILA, National Institute of Standards and Technology and University of Colorado, Boulder, Colorado 80309-0440 and Department of Physics, University of Colorado, Boulder, Colorado 80309-0390 (United States); Demler, Eugene; Lukin, Mikhail D. [Physics Department, Harvard University, Cambridge, Massachusetts 02138 (United States); Kavli Institute for Theoretical Physics, University of California, Santa Barbara, California 93106 (United States); Rey, Ana Maria [JILA, National Institute of Standards and Technology and University of Colorado, Boulder, Colorado 80309-0440 and Department of Physics, University of Colorado, Boulder, Colorado 80309-0390 (United States); Kavli Institute for Theoretical Physics, University of California, Santa Barbara, California 93106 (United States)

2011-09-15T23:59:59.000Z

173

Modelling Alkali Line Absorption and Molecular Bands in Cool DAZs  

E-Print Network (OSTI)

Two peculiar stars showing an apparent extremely broadened and strong NaI D absorption have been discovered in surveys for cool white dwarfs by Oppenheimer et al. (2001) and Harris et al. (SDSS, 2003). We discuss the nature of these objects using PHOENIX atmosphere models for metal-poor brown dwarfs/very low mass stars, and new white dwarf LTE and NLTE models for hydrogen- and helium-dominated atmospheres with metals. These include complete molecular formation in chemical equilibrium and a model for the alkali resonance line broadening based on the damping profiles of Allard et al. (2003), as well as new molecular line opacities for metal hydrides. First results of our calculations indicate good agreement with a hydrogen-dominated WD atmosphere with a Na abundance roughly consistent with a state of high accretion. We analyse deviations of the abundances of Na, K, Mg and Ca from the cosmic pattern and comment on implications of these results for standard accretion scenarios.

Derek Homeier; Nicole F. Allard; France Allard; Peter H. Hauschildt; Andreas Schweitzer; Phillip C. Stancil; Philippe F. Weck

2005-01-05T23:59:59.000Z

174

The Salt Defense Disposal Investigations (SDDI)  

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

Salt Defense Disposal Investigations (SDDI) Salt Defense Disposal Investigations (SDDI) will utilize a newly mined Underground Research Lab (URL) in WIPP to perform a cost effective, proof-of-principle field test of the emplacement of heat-generating radioactive waste and validate modeling efforts. The goals of the SDDI Thermal Test are to: * Demonstrate a proof-of-principle concept for in-drift disposal in salt. * Investigate, in a specific emplacement concept, the response of the salt to heat. * Develop a full-scale response for run-of- mine (ROM) salt. * Develop a validated coupled process model for disposal of heat-generating wastes in salt. * Evaluate the environmental conditions of the

175

The Impact of the Source of Alkali on Sludge Batch 3 Melt Rate (U)  

Science Conference Proceedings (OSTI)

Previous Savannah River National Laboratory (SRNL) melt rate tests in support of the Defense Waste Processing Facility (DWPF) have indicated that improvements in melt rate can be achieved through an increase in the total alkali of the melter feed. Higher alkali can be attained by the use of an ''underwashed'' sludge, a high alkali frit, or a combination of the two. Although the general trend between melt rate and total alkali (in particular Na{sub 2}O content) has been demonstrated, the question of ''does the source of alkali (SOA) matter?'' still exists. Therefore the purpose of this set of tests was to determine if the source of alkali (frit versus sludge) can impact melt rate. The general test concept was to transition from a Na{sub 2}O-rich frit to a Na{sub 2}O-deficient frit while compensating the Na{sub 2}O content in the sludge to maintain the same overall Na{sub 2}O content in the melter feed. Specifically, the strategy was to vary the amount of alkali in frits and in the sludge batch 3 (SB3) sludge simulant (midpoint or baseline feed was SB3/Frit 418 at 35% waste loading) so that the resultant feeds had the same final glass composition when vitrified. A set of SOA feeds using frits ranging from 0 to 16 weight % Na{sub 2}O (in 4% increments) was first tested in the Melt Rate Furnace (MRF) to determine if indeed there was an impact. The dry-fed MRF tests indicated that if the alkali is too depleted from either the sludge (16% Na{sub 2}O feed) or the frit (the 0% Na{sub 2}O feed), then melt rate was negatively impacted when compared to the baseline SB3/Frit 418 feed currently being processed at DWPF. The MRF melt rates for the 4 and 12% SOA feeds were similar to the baseline SB3/Frit 418 (8% SOA) feed. Due to this finding, a smaller subset of SOA feeds that could be processed in the DWPF (4 and 12% SOA feeds) was then tested in the Slurry-fed Melt Rate Furnace (SMRF). The results from a previous SMRF test with SB3/Frit 418 (Smith et al. 2004) were used as the SMRF melt rate of the baseline feed. The SOA SMRF test results agreed with those of the MRF tests for these two feeds as the melt rates were similar to the baseline SB3/Frit 418 feed. In other words, the source of alkali was close enough to the baseline feed as to not negatively impact melt rate. Based on these results, there appears to be an acceptable range of the source of alkali that results in the highest melt rate for a particular sludge batch. If, however, the alkali is too depleted from either the sludge or the frit, then melt rate will be lower. Although SB3 simulant sludge and Frit 418 were used for these tests, it was not the intent of these tests to determine an optimum source of alkali range for SB3. Rather, the findings of these tests should be used to help in the decision process for future sludge batch washing and/or blending strategies. The results, however, do confirm that the current processing of SB3 is being performed in the proper source of alkali range. Because all of this testing was performed on small-scale equipment with slurried, non-radioactive simulant, the exact impact of the source of alkali with SB3 in the DWPF melter could not be fully evaluated.

Smith, M

2005-04-01T23:59:59.000Z

176

SEPARATION OF INORGANIC SALTS FROM ORGANIC SOLUTIONS  

DOE Patents (OSTI)

A process is described for recovering the nitrates of uranium and plutonium from solution in oxygen-containing organic solvents such as ketones or ethers. The solution of such salts dissolved in an oxygen-containing organic compound is contacted with an ion exchange resin whereby sorption of the entire salt on the resin takes place and then the salt-depleted liquid and the resin are separated from each other. The reaction seems to be based on an anion formation of the entire salt by complexing with the anion of the resin. Strong base or quaternary ammonium type resins can be used successfully in this process.

Katzin, L.I.; Sullivan, J.C.

1958-06-24T23:59:59.000Z

177

Results of Salt Batch Qualification Testing  

• Reviews the past campaigns of salt disposition (Macrobatch 1 and 2). ... • Macrobatch 2 processed a total volume of 730,000 gallons from February ...

178

Multiphase Flow and Cavern Abandonment in Salt  

Science Conference Proceedings (OSTI)

This report will explore the hypothesis that an underground cavity in gassy salt will eventually be gas filled as is observed on a small scale in some naturally occurring salt inclusions. First, a summary is presented on what is known about gas occurrences, flow mechanisms, and cavern behavior after abandonment. Then, background information is synthesized into theory on how gas can fill a cavern and simultaneously displace cavern fluids into the surrounding salt. Lastly, two-phase (gas and brine) flow visualization experiments are presented that demonstrate some of the associated flow mechanisms and support the theory and hypothesis that a cavity in salt can become gas filled after plugging and abandonment

Ehgartner, Brian; Tidwell, Vince

2001-02-13T23:59:59.000Z

179

Molten salt safety study. Final report  

DOE Green Energy (OSTI)

The considerations concerning safety in using molten salt (40% potassium nitrate, 60% sodium nitrate) in a solar central receiver plant are addressed. The considerations are of a general nature and do not cover any details of equipment or plant operation. The study includes salt chemical reaction, experiments with molten salt, dry storage and handling constraints, and includes data from the National Fire Protection Association. The contents of this report were evaluated by two utility companies and they concluded that no major safety problems exist in using a molten salt solar system.

Not Available

1980-01-01T23:59:59.000Z

180

Applications of molten salts in plutonium processing  

Science Conference Proceedings (OSTI)

Plutonium is efficiently recovered from scrap at Los Alamos by a series of chemical reactions and separations conducted at temperatures ranging from 700 to 900/sup 0/C. These processes usually employ a molten salt or salt eutectic as a heat sink and/or reaction medium. Salts for these operations were selected early in the development cycle. The selection criteria are being reevaluated. In this article we describe the processes now in use at Los Alamos and our studies of alternate salts and eutectics.

Bowersox, D.F.; Christensen, D.C.; Williams, J.D.

1987-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

,"Natural Gas Salt Caverns Storage Capacity "  

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

Salt Caverns Storage Capacity " ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Natural Gas...

182

Noncentrosymmetric salt inclusion oxides: Role of salt lattices and counter ions in bulk polarity  

SciTech Connect

The synthesis and structural features of a newly emerged class of salt-inclusion solids (SISs) are reviewed. The descriptive chemistry with respect to the role of ionic salt and its correlation with bulk noncentrosymmetricity and polarity of the covalent oxide lattice in question is discussed by means of structure analysis. These unprecedented discoveries have opened doors to novel materials synthesis via the utilities of salt-inclusion chemistry (SIC) that are otherwise known as the molten-salt approach. The result of these investigations prove that the bulk acentricity, or cancellation of which, can be accounted for from the perspective of ionic and/or salt lattices. Highlights: Black-Right-Pointing-Pointer Synthesis and structure of newly emerged salt-inclusion solids are reviewed. Black-Right-Pointing-Pointer Salt lattice and its symmetry correlation with polar framework are discussed. Black-Right-Pointing-Pointer Preservation of acentricity is accounted for from the perspective of ionic and salt lattices.

West, J. Palmer [Department of Chemistry, Clemson University, Clemson, SC 29634-0973 (United States)] [Department of Chemistry, Clemson University, Clemson, SC 29634-0973 (United States); Hwu, Shiou-Jyh, E-mail: shwu@clemson.edu [Department of Chemistry, Clemson University, Clemson, SC 29634-0973 (United States)] [Department of Chemistry, Clemson University, Clemson, SC 29634-0973 (United States)

2012-11-15T23:59:59.000Z

183

Drilling Waste Management Fact Sheet: Disposal in Salt Caverns  

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

Salt Caverns Salt Caverns Fact Sheet - Disposal in Salt Caverns Introduction to Salt Caverns Underground salt deposits are found in the continental United States and worldwide. Salt domes are large, fingerlike projections of nearly pure salt that have risen to near the surface. Bedded salt formations typically contain multiple layers of salt separated by layers of other rocks. Salt beds occur at depths of 500 to more than 6,000 feet below the surface. Schematic Drawing click to view larger image Schematic Drawing of a Cavern in Domal Salt Schematic Drawing click to view larger image Schematic Drawing of a Cavern in Bedded Salt Salt caverns used for oil field waste disposal are created by a process called solution mining. Well drilling equipment is used to drill a hole

184

The direct observation of alkali vapor species in biomass combustion and gasification  

DOE Green Energy (OSTI)

This report summarizes new data from screening various feedstocks for alkali vapor release under combustion conditions. The successful development of a laboratory flow reactor and molecular beam, mass spectrometer interface is detailed. Its application to several herbaceous and woody feedstocks, as well as a fast-pyrolysis oil, under 800 and 1,100{degrees}C batch combustion, is documented. Chlorine seems to play a large role in the facile mobilization of potassium. Included in the report is a discussion of relevant literature on the alkali problem in combustors and turbines. Highlighted are the phenomena identified in studies on coal and methods that have been applied to alkali speciation. The nature of binding of alkali in coal versus biomass is discussed, together with the implications for the ease of release. Herbaceous species and many agricultural residues appear to pose significant problems in release of alkali species to the vapor at typical combustor temperatures. These problems could be especially acute in direct combustion fired turbines, but may be ameliorated in integrated gasification combined cycles.

French, R.J.; Dayton, D.C.; Milne, T.A.

1994-01-01T23:59:59.000Z

185

The Starved Acid Leaching Technology (SALT) for Recovery of ...  

Science Conference Proceedings (OSTI)

Alternative Coolants and Cooling System Designs for Safer Freeze Lined Furnace Operation · Boleo Cobalt Electrowinning Development · Characteristics of ...

186

Dilute acid/metal salt hydrolysis of lignocellulosics - Energy ...  

Building Energy Efficiency ... Solar Thermal; ... loading the impregnated lignocellulosic feedstock into a reactor and heating for a sufficient period of time to ...

187

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

188

Salt Wells Geothermal Exploratory Drilling Program EA  

Open Energy Info (EERE)

Salt Wells Geothermal Exploratory Drilling Program EA Salt Wells Geothermal Exploratory Drilling Program EA (DOI-BLM-NV-C010-2009-0006-EA) Jump to: navigation, search OpenEI Reference LibraryAdd to library Web Site: Salt Wells Geothermal Exploratory Drilling Program EA (DOI-BLM-NV-C010-2009-0006-EA) Abstract No abstract available. Author Bureau of Land Management Published U.S. Department of the Interior- Bureau of Land Management, Carson City Field Office, Nevada, 09/14/2009 DOI Not Provided Check for DOI availability: http://crossref.org Online Internet link for Salt Wells Geothermal Exploratory Drilling Program EA (DOI-BLM-NV-C010-2009-0006-EA) Citation Bureau of Land Management. Salt Wells Geothermal Exploratory Drilling Program EA (DOI-BLM-NV-C010-2009-0006-EA) [Internet]. 09/14/2009. Carson City, NV. U.S. Department of the Interior- Bureau of Land Management,

189

Evaluation of Salt Coolants for Reactor Applications  

SciTech Connect

Molten fluorides were initially developed for use in the nuclear industry as the high-temperature fluid fuel for the Molten Salt Reactor (MSR). The U.S. Department of Energy Office of Nuclear Energy is exploring the use of molten salts as primary and secondary coolants in a new generation of solid-fueled, thermal-spectrum, hightemperature reactors. This paper provides a review of relevant properties for use in evaluation and ranking of salt coolants for high-temperature reactors. Nuclear, physical, and chemical properties were reviewed, and metrics for evaluation are recommended. Chemical properties of the salt were examined to identify factors that affect materials compatibility (i.e., corrosion). Some preliminary consideration of economic factors for the candidate salts is also presented.

Williams, David F [ORNL

2008-01-01T23:59:59.000Z

190

Solid-phase epitaxy of silicon amorphized by implantation of the alkali elements rubidium and cesium  

Science Conference Proceedings (OSTI)

The redistribution of implanted Rb and Cs profiles in amorphous silicon during solid-phase epitaxial recrystallization has been investigated by Rutherford backscattering spectroscopy and secondary ion mass spectroscopy. For the implantation dose used in these experiments, the alkali atoms segregate at the a-Si/c-Si interface during annealing resulting in concentration peaks near the interface. In this way, the alkali atoms are moved towards the surface. Rutherford backscattering spectroscopy in ion channeling configuration was performed to measure average recrystallization rates of the amorphous silicon layers. Preliminary studies on the influence of the alkali atoms on the solid-phase epitaxial regrowth rate reveal a strong retardation compared to the intrinsic recrystallization rate.

Maier, R.; Haeublein, V.; Ryssel, H.; Voellm, H.; Feili, D.; Seidel, H.; Frey, L. [Lehrstuhl fuer Elektronische Bauelemente (LEB), Universitaet Erlangen-Nuernberg, Cauerstrasse 6, 91058 Erlangen (Germany); Fraunhofer-Institut fuer Integrierte Systeme und Bauelementetechnologie (IISB), Schottkystrasse 10, 91058 Erlangen (Germany); Lehrstuhl fuer Elektronische Bauelemente (LEB), Universitaet Erlangen-Nuernberg, Cauerstrasse 6, 91058 Erlangen (Germany) and Fraunhofer-Institut fuer Integrierte Systeme und Bauelementetechnologie (IISB), Schottkystrasse 10, 9 (Germany); Lehrstuhl fuer Mikromechanik, Mikrofluidik/ Mikroaktorik (LMM), Universitaet des Saarlandes, Campus A5.1, 66123 Saarbruecken (Germany); Lehrstuhl fuer Elektronische Bauelemente (LEB), Universitaet Erlangen-Nuernberg, Cauerstrasse 6, 91058 Erlangen (Germany) and Fraunhofer-Institut fuer Integrierte Systeme und Bauelementetechnologie (IISB), Schottkystrasse 10,91 (Germany)

2012-11-06T23:59:59.000Z

191

Laboratory scale vitrification of low-level radioactive nitrate salts and soils from the Idaho National Engineering Laboratory  

SciTech Connect

INEL has radiologically contaminated nitrate salt and soil waste stored above and below ground in Pad A and the Acid Pit at the Radioactive Waste Management Complex. Pad A contain uranium and transuranic contaminated potassium and sodium nitrate salts generated from dewatered waste solutions at the Rocky Flats Plant. The Acid Pit was used to dispose of liquids containing waste mineral acids, uranium, nitrate, chlorinated solvents, and some mercury. Ex situ vitrification is a high temperature destruction of nitrates and organics and immobilizes hazardous and radioactive metals. Laboratory scale melting of actual radionuclides containing INEL Pad A nitrate salts and Acid Pit soils was performed. The salt/soil/additive ratios were varied to determine the range of glass compositions (resulted from melting different wastes); maximize mass and volume reduction, durability, and immobilization of hazardous and radioactive metals; and minimize viscosity and offgas generation for wastes prevalent at INEL and other DOE sites. Some mixtures were spiked with additional hazardous and radioactive metals. Representative glasses were leach tested and showed none. Samples spiked with transuranic showed low nuclide leaching. Wasteforms were two to three times bulk densities of the salt and soil. Thermally co-processing soils and salts is an effective remediation method for destroying nitrate salts while stabilizing the radiological and hazardous metals they contain. The measured durability of these low-level waste glasses approached those of high-level waste glasses. Lab scale vitrification of actual INEL contaminated salts and soils was performed at General Atomics Laboratory as part of the INEL Waste Technology Development and Environmental Restoration within the Buried Waste Integrated Demonstration Program.

Shaw, P. [EG and G Idaho, Inc., Idaho Falls, ID (United States); Anderson, B. [General Atomics, San Diego, CA (United States). NRT Div.; Davis, D. [Envitco Inc., Toledo, OH (United States)

1993-07-01T23:59:59.000Z

192

Modeling of Porous Electrodes in Molten-Salt Systems  

E-Print Network (OSTI)

of Porous Electrodes in Molten-Salt Systems^ John Newmanon High-Temperature Molten Salt B a t - teries, Argonneby the modeling of molten-salt cells, including some

Newman, John

1986-01-01T23:59:59.000Z

193

Direct and Indirect Shortwave Radiative Effects of Sea Salt Aerosols  

Science Conference Proceedings (OSTI)

Sea salt aerosols play a dual role in affecting the atmospheric radiative balance. Directly, sea salt particles scatter the incoming solar radiation and absorb the outgoing terrestrial radiation. By acting as cloud condensation nuclei, sea salt ...

Tarek Ayash; Sunling Gong; Charles Q. Jia

2008-07-01T23:59:59.000Z

194

Geothermometry At Salt Wells Area (Shevenell, Et Al., 2008) ...  

Open Energy Info (EERE)

search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Geothermometry At Salt Wells Area (Shevenell, Et Al., 2008) Exploration Activity Details Location Salt Wells Area...

195

DOE - Office of Legacy Management -- Tatum Salt Dome Test Site...  

Office of Legacy Management (LM)

Tatum Salt Dome Test Site - MS 01 FUSRAP Considered Sites Site: Tatum Salt Dome Test Site (MS.01) Designated Name: Alternate Name: Location: Evaluation Year: Site Operations: Site...

196

EIA - Natural Gas Pipeline Network - Salt Cavern Storage Reservoir...  

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

Salt Cavern Underground Natural Gas Storage Reservoir Configuration Salt Cavern Underground Natural Gas Storage Reservoir Configuration Source: PB Energy Storage Services Inc....

197

Notice of Availability of Section 3116 Determination for Salt...  

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

Notice of Availability of Section 3116 Determination for Salt Waste Disposal at the Savannah River Site Notice of Availability of Section 3116 Determination for Salt Waste Disposal...

198

Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot...  

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

Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Granular Salt Consolidation, Constitutive Model and Micromechanics Coupled Thermal-Hydrological-Mechanical Processes...

199

Molten Salt Breeder Reactors Academia Sinica, ITRI, NTHU  

E-Print Network (OSTI)

Power 4/8/12 Frank H. Shu Gen IV MSBR/LFTR Liquid fuel (molten salt) Molten salt coolant (unpopulated

Wang, Ming-Jye

200

Independent Oversight Review, Savannah River Site Salt Waste...  

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

Savannah River Site Salt Waste Processing Facility - August 2013 Independent Oversight Review, Savannah River Site Salt Waste Processing Facility - August 2013 August 2013 Review...

Note: This page contains sample records for the topic "acids alkalies salts" 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

Corrosion of High Temperature Alloys in Molten Salts  

Science Conference Proceedings (OSTI)

Fluoride and chloride salts are among the candidates for this application. However, materials corrosion is an issue in these molten salts, particularly in molten ...

202

Category:Salt Lake City, UT | Open Energy Information  

Open Energy Info (EERE)

UT UT Jump to: navigation, search Go Back to PV Economics By Location Media in category "Salt Lake City, UT" The following 16 files are in this category, out of 16 total. SVFullServiceRestaurant Salt Lake City UT Moon Lake Electric Assn Inc (Utah).png SVFullServiceRestauran... 57 KB SVHospital Salt Lake City UT Moon Lake Electric Assn Inc (Utah).png SVHospital Salt Lake C... 57 KB SVLargeHotel Salt Lake City UT Moon Lake Electric Assn Inc (Utah).png SVLargeHotel Salt Lake... 55 KB SVLargeOffice Salt Lake City UT Moon Lake Electric Assn Inc (Utah).png SVLargeOffice Salt Lak... 57 KB SVMediumOffice Salt Lake City UT Moon Lake Electric Assn Inc (Utah).png SVMediumOffice Salt La... 62 KB SVMidriseApartment Salt Lake City UT Moon Lake Electric Assn Inc (Utah).png

203

NOVEL REFRACTORY MATERIALS FOR HIGH ALKALI, HIGH TEMPERATURE ENVIRONMENTS  

SciTech Connect

A project was led by Oak Ridge National Laboratory (ORNL) in collaboration with a research team comprised of the academic institution Missouri University of Science and Technology (MS&T), and the industrial company MINTEQ International, Inc. (MINTEQ), along with representatives from the aluminum, chemical, glass, and forest products industries. The project was to address the need for new innovative refractory compositions by developing a family of novel MgO-Al 2O3, MgAl2O4, or other similar spinel structured or alumina-based unshaped refractory compositions (castables, gunnables, shotcretes, etc.) utilizing new aggregate materials, bond systems, protective coatings, and phase formation techniques (in-situ phase formation, altered conversion temperatures, accelerated reactions, etc). This family of refractory compositions would then be tailored for use in high-temperature, high-alkaline industrial environments like those found in the aluminum, chemical, forest products, glass, and steel industries. Both practical refractory development experience and computer modeling techniques were used to aid in the design of this new family of materials. The newly developed materials were expected to offer alternative material choices for high-temperature, high-alkali environments that were capable of operating at higher temperatures (goal of increasing operating temperature by 100-200oC depending on process) or for longer periods of time (goal of twice the life span of current materials or next process determined service increment). This would lead to less process down time, greater energy efficiency for associated manufacturing processes (more heat kept in process), and materials that could be installed/repaired in a more efficient manner. The overall project goal was a 5% improvement in energy efficiency (brought about through a 20% improvement in thermal efficiency) resulting in a savings of 3.7 TBtu/yr (7.2 billion ft3 natural gas) by the year 2030. Additionally, new application techniques and systems were developed as part of this project to optimize the installation of this new family of refractory materials to maximize the properties of installed linings and to facilitate nuances such as hot installation and repair. Under this project, seven new shotcrete materials were developed for both primary and repair applications in aluminum, black liquor, coal gasification, and lime kiln environments. Developed materials were based on alumino-silicate, magnesia, and spinel forming systems. One of the developed materials was an insulating shotcrete to be used behind the high conductivity spinel linings developed under this project. Fundamental research work was carried out at MS&T throughout the life of the project to provide support for the development and production of the experimental refractory materials being developed. Work was also ongoing at ORNL and MS&T through the duration of the project on the measurement and characterization of key refractory properties as identified during year one of the project. Both materials currently being used in the industrial processes as identified and supplied by the industrial partners of this project and new materials being provided and developed by MINTEQ were evaluated as necessary. Additionally, energy savings estimates based on measured properties of the experimentally developed refractory systems from this project were made at MINTEQ to validate the energy savings estimates originally proposed for the project. As another part of the project, on-line inspection and hot repair techniques were considered. It was determined that although repair materials were successfully developed under this project for aluminum, black liquor, and coal gasification systems which enable hot repair, there was only minor interest from industry in implementing these materials. On-line inspection techniques were also identified under this project which are currently used in the steel industry, but implementation of these techniques in applications such as black liquor and coal gasification where higher temperature

Hemrick, James Gordon [ORNL; Smith, Jeffrey D [ORNL; O'Hara, Kelley [University of Missouri, Rolla; Rodrigues-Schroer, Angela [Minteq International, Inc.; Colavito, [Minteq International, Inc.

2012-08-01T23:59:59.000Z

204

Anaerobic Baffled Reactor (ABR) for Alkali-minimization Dyeing-printing Wastewater Biodegradation  

Science Conference Proceedings (OSTI)

The performance of the laboratory scale anaerobic baffled reactor (ABR) was investigated by the use of granular sludge to treat alkali-minimization and dyeing-printing wastewater (ADW-water). The experiment showed that the start-up of reactor was completed ... Keywords: ABR, ADW-water, Granular sludge, UV254, VFA

Qijun Zhong; Bo Yang

2012-05-01T23:59:59.000Z

205

Alkali slurry ozonation to produce a high capacity nickel battery material  

DOE Patents (OSTI)

A high capacity battery material is made, consisting essentially of hydrated Ni(II) hydroxide, and about 5 wt. % to about 40 wt. % of Ni(IV) hydrated oxide interlayer doped with alkali metal cations selected from potassium, sodium and lithium cations.

Jackovitz, John F. (Monroeville, PA); Pantier, Earl A. (Penn Hills, PA)

1984-11-06T23:59:59.000Z

206

Secondary cell with orthorhombic alkali metal/manganese oxide phase active cathode material  

DOE Patents (OSTI)

An alkali metal manganese oxide secondary cell is disclosed which can provide a high rate of discharge, good cycling capabilities, good stability of the cathode material, high specific energy (energy per unit of weight) and high energy density (energy per unit volume). The active material in the anode is an alkali metal and the active material in the cathode comprises an orthorhombic alkali metal manganese oxide which undergoes intercalation and deintercalation without a change in phase, resulting in a substantially linear change in voltage with change in the state of charge of the cell. The active material in the cathode is an orthorhombic structure having the formula M{sub x}Z{sub y}Mn{sub (1{minus}y)}O{sub 2}, where M is an alkali metal; Z is a metal capable of substituting for manganese in the orthorhombic structure such as iron, cobalt or titanium; x ranges from about 0.2 in the fully charged state to about 0.75 in the fully discharged state, and y ranges from 0 to 60 atomic %. Preferably, the cell is constructed with a solid electrolyte, but a liquid or gelatinous electrolyte may also be used in the cell. 11 figs.

Doeff, M.M.; Peng, M.Y.; Ma, Y.; Visco, S.J.; DeJonghe, L.C.

1996-09-24T23:59:59.000Z

207

Salt Wells Geothermal Area | Open Energy Information  

Open Energy Info (EERE)

Salt Wells Geothermal Area Salt Wells Geothermal Area (Redirected from Salt Wells Area) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Geothermal Resource Area: Salt Wells Geothermal Area Contents 1 Area Overview 2 History and Infrastructure 3 Regulatory and Environmental Issues 4 Future Plans 5 Exploration History 6 Well Field Description 7 Research and Development Activities 8 Technical Problems and Solutions 9 Geology of the Area 9.1 Regional Setting 9.2 Stratigraphy 9.3 Structure 10 Hydrothermal System 11 Heat Source 12 Geofluid Geochemistry 13 NEPA-Related Analyses (9) 14 Exploration Activities (28) 15 References Area Overview Geothermal Area Profile Location: Nevada Exploration Region: Northwest Basin and Range Geothermal Region GEA Development Phase: Operational"Operational" is not in the list of possible values (Phase I - Resource Procurement and Identification, Phase II - Resource Exploration and Confirmation, Phase III - Permitting and Initial Development, Phase IV - Resource Production and Power Plant Construction) for this property.

208

Salt Lake City- High Performance Buildings Requirement  

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

Salt Lake City's mayor issued an executive order in July 2005 requiring that all public buildings owned and controlled by the city be built or renovated to meet the requirements of LEED "silver"...

209

Salt Dispersion in the Hudson Estuary  

Science Conference Proceedings (OSTI)

The seaward transport of salt by river discharge through an estuary is balanced under steady conditions by landward dispersion effected by various physical mixing processes. Observations of current and salinity in the lower Hudson estuary provide ...

Kenneth Hunkins

1981-05-01T23:59:59.000Z

210

Molten salt destruction of energetic waste materials  

DOE Patents (OSTI)

A molten salt destruction process is used to treat and destroy energetic waste materials such as high explosives, propellants, and rocket fuels. The energetic material is pre-blended with a solid or fluid diluent in safe proportions to form a fluid fuel mixture. The fuel mixture is rapidly introduced into a high temperature molten salt bath. A stream of molten salt is removed from the vessel and may be recycled as diluent. Additionally, the molten salt stream may be pumped from the reactor, circulated outside the reactor for further processing, and delivered back into the reactor or cooled and circulated to the feed delivery system to further dilute the fuel mixture entering the reactor.

Brummond, William A. (Livermore, CA); Upadhye, Ravindra S. (Pleasanton, CA); Pruneda, Cesar O. (Livermore, CA)

1995-01-01T23:59:59.000Z

211

Molten salt destruction of energetic waste materials  

DOE Patents (OSTI)

A molten salt destruction process is used to treat and destroy energetic waste materials such as high explosives, propellants, and rocket fuels. The energetic material is pre-blended with a solid or fluid diluent in safe proportions to form a fluid fuel mixture. The fuel mixture is rapidly introduced into a high temperature molten salt bath. A stream of molten salt is removed from the vessel and may be recycled as diluent. Additionally, the molten salt stream may be pumped from the reactor, circulated outside the reactor for further processing, and delivered back into the reactor or cooled and circulated to the feed delivery system to further dilute the fuel mixture entering the reactor. 4 figs.

Brummond, W.A.; Upadhye, R.S.; Pruneda, C.O.

1995-07-18T23:59:59.000Z

212

PROCESSING OF MOLTEN SALT POWER REACTOR FUEL  

SciTech Connect

ABS> Fuel reprocessing methods are being investigated for molten salt nuclear reactors which use LiF--BeF/sub 2/ salt as a solvent for UF/sub 4/ and ThF/sub 4/. A liquid HF dissolution procedure coupled with fluorination has been developed for recovery of the uranium and LiF- BeF/sub 2/ solvent salt which is highly enriched in Li/sup 7/. The recovered salt is decontaminated in the process from the major reactor poisons; namely, rare earths and neptunium. A brief investigation of alternate methods, including oxide precipitation, partial freezing, and metal reduction, indicated that such methods may give some separation of the solvent salt from reactor poisons, but they do not appear to be sufficiently quantitative for a simple processing operation. Solubilities of LiF and BeF/sub 2/ in aqueous 70t0 100% HF are presented. The BeF/sub 2/ solubility is appreciably increased in the presence of water and large amounts of LiF. Salt solubilities of 150 g/liter are attainable. Tracer experiments indicate that rare earth solubilities, relative to LiF-- BeF/sub 2/ solvent salt solubility, increase from about 10/sup -4/ mole% in 98% HF to 0.003 mole% in 80% HF. Fluorination of uranium from LiF--BeF/sub 2/ salt was demonstrated. This appears feasible also for the recovery of the relatively small ccncentration of uranium produced in the LiF- BeF/sub 2/ThF/sub 4/ blanket. A proposed chemical flowsheet is presented on the basis of this exploratory work as applied to the semicontinuous processing of a 600 Mw power reactor. (auth)

Campbell, D.O.; Cathers, G.I.

1959-04-01T23:59:59.000Z

213

Thermal Characterization of Molten Salt Systems  

Science Conference Proceedings (OSTI)

The phase stability of molten salts in an electrorefiner (ER) may be adversely affected by the buildup of sodium, fission products, and transuranics in the electrolyte. Potential situations that need to be avoided are the following: (1) salt freezing due to an unexpected change in the liquidus temperature, (2) phase separation or non-homogeneity of the molten salt due to the precipitation of solids or formation of immiscible liquids, and (3) any mechanism that can result in the separation and concentration of fissile elements from the molten salt. Any of these situations would result in an off-normal condition outside the established safety basis for electrorefiner (ER) operations. The stability (and homogeneity) of the phases can potentially be monitored through the thermal characterization of the salts, which can be a function of impurity concentration. This report describes the experimental results of typical salts compositions, which consist of chlorides of potassium, lithium, strontium, samarium, praseodymium, lanthanum, barium, cerium, cesium, neodymium, sodium and gadolinium chlorides as a surrogate for both uranium and plutonium, used for the processing of used nuclear fuels.

Toni Y. Gutknecht; Guy L. Fredrickson

2011-09-01T23:59:59.000Z

214

HELSINKI UNIVERSITY OF TECHNOLOGY ENE-47.153 Trace elements and alkaliTrace elements and alkali  

E-Print Network (OSTI)

REGULATIONS Although incinerator flue gas emission limits for acid gases have been imposed by the federal, such as sodium chlorite (NaCI02), is added to oxidize flue gas NO to N02, which can be removed by a sodium of saturated flue gas to approximately 60°C ( 140°F), the total (par ticulate and gaseous) mercury emissions

Zevenhoven, Ron

215

Brines formed by multi-salt deliquescence  

SciTech Connect

The FY05 Waste Package Environment testing program at Lawrence Livermore National Laboratory focused on determining the temperature, relative humidity, and solution compositions of brines formed due to the deliquescence of NaCl-KNO{sub 3}-NaNO{sub 3} and NaCl-KNO{sub 3}-NaNO{sub 3}-Ca(NO{sub 3}){sub 2} salt mixtures. Understanding the physical and chemical behavior of these brines is important because they define conditions under which brines may react with waste canister surfaces. Boiling point experiments show that NaCl-KNO{sub 3}-NaNO{sub 3} and NaCl-KNO{sub 3}-NaNO{sub 3}-Ca(NO{sub 3}){sub 2} salt mixtures form brines that transform to hydrous melts that do not truly 'dry out' until temperatures exceed 300 and 400 C, respectively. Thus a conducting solution is present for these salt assemblages over the thermal history of the repository. The corresponding brines form at lower relative humidity at higher temperatures. The NaCl-KNO{sub 3}-NaNO{sub 3} salt mixture has a mutual deliquescence relative humidity (MDRH) of 25.9% at 120 C and 10.8% at 180 C. Similarly, the KNO{sub 3}-NaNO{sub 3} salt mixture has MDRH of 26.4% at 120 C and 20.0% at 150 C. The KNO{sub 3}-NaNO{sub 3} salt mixture salts also absorb some water (but do not appear to deliquesce) at 180 C and thus may also contribute to the transfer of electrons at interface between dust and the waste package surface. There is no experimental evidence to suggest that these brines will degas and form less deliquescent salt assemblages. Ammonium present in atmospheric and tunnel dust (as the chloride, nitrate, or sulfate) will readily decompose in the initial heating phase of the repository, and will affect subsequent behavior of the remaining salt mixture only through the removal of a stoichiometric equivalent of one or more anions. Although K-Na-NO{sub 3}-Cl brines form at high temperature and low relative humidity, these brines are dominated by nitrate, which is known to inhibit corrosion at lower temperature. Nitrate to chloride ratios of the NaCl-KNO{sub 3}-NaNO{sub 3} salt mixture are about NO{sub 3}:Cl = 19:1. The role of nitrate on corrosion at higher temperatures is addressed in a companion report (Dixit et al., 2005).

Carroll, S; Rard, J; Alai, M; Staggs, K

2005-11-04T23:59:59.000Z

216

Waste Isolation Pilot Plant's Excavated Salt Agreement Supports  

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

Waste Isolation Pilot Plant's Excavated Salt Agreement Supports Waste Isolation Pilot Plant's Excavated Salt Agreement Supports Conservation Education, Other Public Initiatives Waste Isolation Pilot Plant's Excavated Salt Agreement Supports Conservation Education, Other Public Initiatives November 14, 2013 - 12:00pm Addthis Approximately 1.8 million tons of salt have been mined out of the underground at WIPP. Approximately 1.8 million tons of salt have been mined out of the underground at WIPP. Proceeds from the WIPP salt allowed hundreds of southeast New Mexico students to learn about resource conservation. Proceeds from the WIPP salt allowed hundreds of southeast New Mexico students to learn about resource conservation. The crushed salt is used as a supplement in cattle feed. Since the salt from WIPP has been mined from the middle of a large salt formation, its quality is high, according to Magnum Minerals.

217

Waste Isolation Pilot Plant's Excavated Salt Agreement Supports  

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

Waste Isolation Pilot Plant's Excavated Salt Agreement Supports Waste Isolation Pilot Plant's Excavated Salt Agreement Supports Conservation Education, Other Public Initiatives Waste Isolation Pilot Plant's Excavated Salt Agreement Supports Conservation Education, Other Public Initiatives November 14, 2013 - 12:00pm Addthis Approximately 1.8 million tons of salt have been mined out of the underground at WIPP. Approximately 1.8 million tons of salt have been mined out of the underground at WIPP. Proceeds from the WIPP salt allowed hundreds of southeast New Mexico students to learn about resource conservation. Proceeds from the WIPP salt allowed hundreds of southeast New Mexico students to learn about resource conservation. The crushed salt is used as a supplement in cattle feed. Since the salt from WIPP has been mined from the middle of a large salt formation, its quality is high, according to Magnum Minerals.

218

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

219

Plutonium and americium recovery from spent molten-salt-extraction salts with aluminum-magnesium alloys  

Science Conference Proceedings (OSTI)

Development work was performed to determine the feasibility of removing plutonium and americium from spent molten-salt-extraction (MSE) salts using Al-Mg alloys. If the product buttons from this process are compatible with subsequent aqueous processing, the complex chloride-to-nitrate aqueous conversion step which is presently required for these salts may be eliminated. The optimum alloy composition used to treat spent 8 wt % MSE salts in the past yielded poor phase-disengagement characteristics when applied to 30 mol % salts. After a limited investigation of other alloy compositions in the Al-Mg-Pu-Am system, it was determined that the Al-Pu-Am system could yield a compatible alloy. In this system, experiments were performed to investigate the effects of plutonium loading in the alloy, excess magnesium, age of the spent salt on actinide recovery, phase disengagement, and button homogeneity. Experimental results indicate that 95 percent plutonium recoveries can be attained for fresh salts. Further development is required for backlog salts generated prior to 1981. A homogeneous product alloy, as required for aqueous processing, could not be produced.

Cusick, M.J.; Sherwood, W.G.; Fitzpatrick, R.F.

1984-04-23T23:59:59.000Z

220

Salt Mechanics Primer for Near-Salt and Sub-Salt Deepwater Gulf of Mexico Field Developments  

Science Conference Proceedings (OSTI)

The Gulf of Mexico (GoM) is the most active deepwater region in the world and provides some of the greatest challenges in scope and opportunity for the oil and gas industry. The complex geologic settings and significant water and reservoir depths necessitate high development costs, in addition to requiring innovating technology. The investment costs are substantial: because of the extreme water depths (up to 8000 feet) and considerable reservoir depths (to 30,000 feet below mudline), the cost of drilling a single well can be upwards of 50 to 100 million dollars. Central, therefore, to successful economic exploitation are developments with a minimum number of wells combined with a well service lifetime of twenty to thirty years. Many of the wells that are planned for the most significant developments will penetrate thick salt formations, and the combined drilling costs for these fields are estimated in the tens of billions of dollars. In May 2001, Sandia National Laboratories initiated a Joint Industry Project focused on the identification, quantification, and mitigation of potential well integrity issues associated with sub-salt and near-salt deepwater GoM reservoirs. The project is jointly funded by the DOE (Natural Gas and Oil Technology Partnership) and nine oil companies (BHP Billiton Petroleum, BP, ChevronTexaco, Conoco, ExxonMobil, Halliburton, Kerr-McGee, Phillips Petroleum, and Shell). This report provides an assessment of the state of the art of salt mechanics, and identifies potential well integrity issues relevant to deepwater GoM field developments. Salt deformation is discussed and a deformation mechanism map is provided for salt. A bounding steady-state strain rate contour map is constructed for deepwater GoM field developments, and the critical issue of constraint in the subsurface, and resultant necessity for numerical analyses is discussed.

FOSSUM, ARLO F.; FREDRICH, JOANNE T.

2002-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Corrosion of aluminides by molten nitrate salt  

DOE Green Energy (OSTI)

The corrosion of titanium-, iron-, and nickel-based aluminides by a highly aggressive, oxidizing NaNO{sub 3}(-KNO{sub 3})-Na{sub 2}O{sub 2} has been studied at 650{degree}C. It was shown that weight changes could be used to effectively evaluate corrosion behavior in the subject nitrate salt environments provided these data were combined with salt analyses and microstructural examinations. The studies indicated that the corrosion of relatively resistant aluminides by these nitrate salts proceeded by oxidation and a slow release from an aluminum-rich product layer into the salt at rates lower than that associated with many other types of metallic materials. The overall corrosion process and resulting rate depended on the particular aluminide being exposed. In order to minimize corrosion of nickel or iron aluminides, it was necessary to have aluminum concentrations in excess of 30 at. %. However, even at a concentration of 50 at. % Al, the corrosion resistance of TiAl was inferior to that of Ni{sub 3}Al and Fe{sub 3}Al. At higher aluminum concentrations, iron, nickel, and iron-nickel aluminides exhibited quite similar weight changes, indicative of the principal role of aluminum in controlling the corrosion process in NaNO{sub 3}(-KNO{sub 3})-Na{sub 2}O{sub 2} salts. 20 refs., 5 figs., 3 tabs.

Tortorelli, P.F.; Bishop, P.S.

1990-01-01T23:59:59.000Z

222

SEPARATION PROCESS FOR THORIUM SALTS  

DOE Patents (OSTI)

A process is described for the separation of uranium, thorium, and rare earths extracted from monazite by digesting with sulfuric acid. By carefully increasing the pH of the solution, stepwise, over the range 0.8 to 5.5, a series of selective precipitations will be achieved, with the thorium values coming out at lower pH, the rare earths at intermediate pH and the uranium last. Some mixed precipitates will be obtained, and these may be treated by dissolving in HNO/sub 3/ and contacting with dibutyl phosphate, whereby thorium or uranium are taken up by the organic phase while the rare earths preferentially remain in the aqueous solution.

Bridger, G.L.; Whatley, M.E.; Shaw, K.G.

1957-12-01T23:59:59.000Z

223

Salt Wells Geothermal Area | Open Energy Information  

Open Energy Info (EERE)

Salt Wells Geothermal Area Salt Wells Geothermal Area Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Geothermal Resource Area: Salt Wells Geothermal Area Contents 1 Area Overview 2 History and Infrastructure 3 Regulatory and Environmental Issues 4 Future Plans 5 Exploration History 6 Well Field Description 7 Research and Development Activities 8 Technical Problems and Solutions 9 Geology of the Area 9.1 Regional Setting 9.2 Stratigraphy 9.3 Structure 10 Hydrothermal System 11 Heat Source 12 Geofluid Geochemistry 13 NEPA-Related Analyses (9) 14 Exploration Activities (28) 15 References Area Overview Geothermal Area Profile Location: Nevada Exploration Region: Northwest Basin and Range Geothermal Region GEA Development Phase: Operational"Operational" is not in the list of possible values (Phase I - Resource Procurement and Identification, Phase II - Resource Exploration and Confirmation, Phase III - Permitting and Initial Development, Phase IV - Resource Production and Power Plant Construction) for this property.

224

Salt Wells Geothermal Project | Open Energy Information  

Open Energy Info (EERE)

Salt Wells Geothermal Project Salt Wells Geothermal Project Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Development Project: Salt Wells Geothermal Project Project Location Information Coordinates 39.580833333333°, -118.33444444444° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":39.580833333333,"lon":-118.33444444444,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

225

Brine flow in heated geologic salt.  

Science Conference Proceedings (OSTI)

This report is a summary of the physical processes, primary governing equations, solution approaches, and historic testing related to brine migration in geologic salt. Although most information presented in this report is not new, we synthesize a large amount of material scattered across dozens of laboratory reports, journal papers, conference proceedings, and textbooks. We present a mathematical description of the governing brine flow mechanisms in geologic salt. We outline the general coupled thermal, multi-phase hydrologic, and mechanical processes. We derive these processes' governing equations, which can be used to predict brine flow. These equations are valid under a wide variety of conditions applicable to radioactive waste disposal in rooms and boreholes excavated into geologic salt.

Kuhlman, Kristopher L.; Malama, Bwalya

2013-03-01T23:59:59.000Z

226

Molten nitrate salt technology development status report  

SciTech Connect

Recognizing thermal energy storage as potentially critical to the successful commercialization of solar thermal power systems, the Department of Energy (DOE) has established a comprehensive and aggressive thermal energy storage technology development program. Of the fluids proposed for heat transfer and energy storage molten nitrate salts offer significant economic advantages. The nitrate salt of most interest is a binary mixture of NaNO/sub 3/ and KNO/sub 3/. Although nitrate/nitrite mixtures have been used for decades as heat transfer and heat treatment fluids the use has been at temperatures of about 450/sup 0/C and lower. In solar thermal power systems the salts will experience a temperature range of 350 to 600/sup 0/C. Because central receiver applications place more rigorous demands and higher temperatures on nitrate salts a comprehensive experimental program has been developed to examine what effects, if any, the new demands and temperatures have on the salts. The experiments include corrosion testing, environmental cracking of containment materials, and determinations of physical properties and decomposition mechanisms. This report details the work done at Sandia National Laboratories in each area listed. In addition, summaries of the experimental programs at Oak Ridge National Laboratory, the University of New York, EIC Laboratories, Inc., and the Norwegian Institute of Technology on molten nitrate salts are given. Also discussed is how the experimental programs will influence the near-term central receiver programs such as utility repowering/industrial retrofit and cogeneration. The report is designed to provide easy access to the latest information and data on molten NaNO/sub 3//KNO/sub 3/ for the designers and engineers of future central receiver projects.

Carling, R.W.; Kramer, C.M.; Bradshaw, R.W.; Nissen, D.A.; Goods, S.H.; Mar, R.W.; Munford, J.W.; Karnowsky, M.M.; Biefeld, R.N.; Norem, N.J.

1981-03-01T23:59:59.000Z

227

Fast Spectrum Molten Salt Reactor Options  

DOE Green Energy (OSTI)

During 2010, fast-spectrum molten-salt reactors (FS-MSRs) were selected as a transformational reactor concept for light-water reactor (LWR)-derived heavy actinide disposition by the Department of Energy-Nuclear Energy Advanced Reactor Concepts (ARC) program and were the subject of a preliminary scoping investigation. Much of the reactor description information presented in this report derives from the preliminary studies performed for the ARC project. This report, however, has a somewhat broader scope-providing a conceptual overview of the characteristics and design options for FS-MSRs. It does not present in-depth evaluation of any FS-MSR particular characteristic, but instead provides an overview of all of the major reactor system technologies and characteristics, including the technology developments since the end of major molten salt reactor (MSR) development efforts in the 1970s. This report first presents a historical overview of the FS-MSR technology and describes the innovative characteristics of an FS-MSR. Next, it provides an overview of possible reactor configurations. The following design features/options and performance considerations are described including: (1) reactor salt options-both chloride and fluoride salts; (2) the impact of changing the carrier salt and actinide concentration on conversion ratio; (3) the conversion ratio; (4) an overview of the fuel salt chemical processing; (5) potential power cycles and hydrogen production options; and (6) overview of the performance characteristics of FS-MSRs, including general comparative metrics with LWRs. The conceptual-level evaluation includes resource sustainability, proliferation resistance, economics, and safety. The report concludes with a description of the work necessary to begin more detailed evaluation of FS-MSRs as a realistic reactor and fuel cycle option.

Gehin, Jess C [ORNL; Holcomb, David Eugene [ORNL; Flanagan, George F [ORNL; Patton, Bruce W [ORNL; Howard, Rob L [ORNL; Harrison, Thomas J [ORNL

2011-07-01T23:59:59.000Z

228

Heated muds solve squeezing-salt problems  

Science Conference Proceedings (OSTI)

Squeezing salts have been responsible for major drilling problems in many areas of the world for over half a century. In NAM's area of operations, they occur primarily in the Zechstein group of evaporites. They are responsible for problems such as stuck pipe during drilling and casing failure during both drilling and casing failure during both drilling and production, sometimes as much as 12 years after drilling. Since 1960, some US $170 million (at 1992 drilling costs) have been spent redrilling wells with failed casing strings. In 1991, NAM was associated with a Billiton project to drill 2 wells for the solution mining of magnesium and potassium salts. Gauge holes were a prerequisite to identify the objective salts by electric logging. Excellent results were achieved by drilling with a heated salt mud that had been saturated on surface to downhole conditions. The heating requirements for the Billiton project were modest, as the top of the squeezing salt occurred at approximately 1,500 m (4,920 ft), requiring a circulating temperature of 45 C (113 F) to achieve the necessary saturation level. However, in NAM's operations, the top of the squeezing salt generally occurs between 2.500 m and 3,000 m (8,200 ft and 9,850 ft), requiring temperatures on the order of 70 C (158 F). Despite the need for higher temperatures, the success of the Billiton project prompted NAM to introduce the heating system on a trial basis. To date eight wells have been drilled using the system, resulting in the drilling of a virtual gauge hole with successful cementations being achieved in each case.

Muecke, N.B. (Nederlandse Aardolie, Maatschappij (Netherlands))

1993-11-01T23:59:59.000Z

229

Effect of cofiring coal and biofuel with sewage sludge on alkali problems in a circulating fluidized bed boiler  

Science Conference Proceedings (OSTI)

Cofiring experiments were performed in a 12 MW circulating fluidized bed boiler. The fuel combinations were biofuel (wood+straw), coal+biofuel, coal+sewage sludge+biofuel, and sewage sludge+biofuel. Limestone or chlorine (PVC) was added in separate experiments. Effects of feed composition on bed ash and fly ash were examined. The composition of flue gas was measured, including on-line measurement of alkali chlorides. Deposits were collected on a probe simulating a superheater tube. It was found that the fuel combination, as well as addition of limestone, has little effect on the alkali fraction in bed ash, while chlorine decreases the alkali fraction in bed ash. Sewage sludge practically eliminates alkali chlorides in flue gas and deposits. Addition of enough limestone to coal and sludge for elimination of the SO{sub 2} emission does not change the effect of chlorine. Chlorine addition increases the alkali chloride in flue gas, but no chlorine was found in the deposits with sewage sludge as a cofuel. Cofiring of coal and biofuel lowers the alkali chloride concentration in the flue gas to about a third compared with that of pure biofuel. This is not affected by addition of lime or chlorine. It is concluded that aluminum compounds in coal and sludge are more important than sulfur to reduce the level of KCl in flue gas and deposits. 24 refs., 8 figs., 7 tabs.

K.O. Davidsson; L.-E. Aamand; A.-L. Elled; B. Leckner [Chalmers University of Technology, Goeteborg (Sweden). Department of Energy and Environment

2007-12-15T23:59:59.000Z

230

Alkali or alkaline earth metal promoted catalyst and a process for methanol synthesis using alkali or alkaline earth metals as promoters  

DOE Patents (OSTI)

The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a heterogeneous catalyst comprising reduced copper chromite impregnated with an alkali or alkaline earth metal. There is thus no need to add a separate alkali or alkaline earth compound. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100--160 C and the pressure range of 40--65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H[sub 2]/CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

Tierney, J.W.; Wender, I.; Palekar, V.M.

1995-01-31T23:59:59.000Z

231

Alkali or alkaline earth metal promoted catalyst and a process for methanol synthesis using alkali or alkaline earth metals as promoters  

DOE Patents (OSTI)

The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a heterogeneous catalyst comprising reduced copper chromite impregnated with an alkali or alkaline earth metal. There is thus no need to add a separate alkali or alkaline earth compound. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100.degree.-160.degree. C. and the pressure range of 40-65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H.sub.2 /CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

Tierney, John W. (Pittsburgh, PA); Wender, Irving (Pittsburgh, PA); Palekar, Vishwesh M. (Pittsburgh, PA)

1995-01-01T23:59:59.000Z

232

CANMET/Industry Research Consortium on Alkali-Aggregate Reactivity in Concrete  

Science Conference Proceedings (OSTI)

The alkali-silica reaction (ASR) is a deleterious chemical reaction that can result in the deterioration of concrete structures. This report presents the results of a research and development study, funded by a broadly-based multi-national industry consortium, that is developing an engineering database on the long-term effectiveness of fly ash and other supplementary cementing materials (SCMs) in counteracting ASR in concrete.

2001-12-11T23:59:59.000Z

233

The Role of High Calcium Fly Ashes in Controlling Alkali-Silica Reactions in Concrete  

Science Conference Proceedings (OSTI)

The alkali-silica reaction (ASR) is a deleterious chemical reaction that can result in the deterioration of concrete structures. This report builds upon the results of a research and development study, funded by a broadly-based multi-national industry consortium, that is developing an engineering database on the long-term effectiveness of Class F fly ash and other supplementary cementing materials (SCMs) in counteracting ASR in concrete.

2002-11-20T23:59:59.000Z

234

SAFETY CONSIDERATIONS FOR HANDLING PLUTONIUM, URANIUM, THORIUM, THE ALKALI METALS, ZIRCONIUM, TITANIUM, MAGNESIUM, AND CALCIUM  

SciTech Connect

BS>This report compiles from various sources safety considerations for work with the special metals plutonium, uranium, thorium, the alkali group, magnesium, titanium, calcium, and zirconium. General criteria to be observed in handling all of these metals and their alloys are listed, as well as characteristics of individual metals with regard to health hazards, pyrophoricity, explosiveness, and other chemical reactions, in both handling and storage. (auth)

Stout, E.L. comp.

1957-09-01T23:59:59.000Z

235

Mineralogy, geochemistry and expansion testing of an alkali-reactive basalt from western Anatolia, Turkey  

Science Conference Proceedings (OSTI)

In this paper, the alkali-silica reaction performance of a basalt rock from western Anatolia, Turkey is reported. It is observed that the rock causes severe gel formation in the concrete microbar test. It appears that the main source of expansion is the reactive glassy phase of the basalt matrix having approximately 70% of SiO{sub 2}. The study presents the microstructural characteristics of unreacted and reacted basalt aggregate by optical and electron microscopy and discusses the possible reaction mechanism. Microstructural analysis revealed that the dissolution of silica is overwhelming in the matrix of the basalt and it eventually generates four consequences: (1) Formation of alkali-silica reaction gel at the aggregate perimeter, (2) increased porosity and permeability of the basalt matrix, (3) reduction of mechanical properties of the aggregate and (4) additional gel formation within the aggregate. It is concluded that the basalt rock is highly prone to alkali-silica reaction. As an aggregate, this rock is not suitable for concrete production.

Copuroglu, Oguzhan, E-mail: O.Copuroglu@CiTG.TUDelft.NL [Delft University of Technology, Faculty of CiTG, Materials and Environment, Stevinweg 1, 2628CN, Delft (Netherlands); Andic-Cakir, Ozge [Ege University, Civil Engineering Dept., 35100 Bornova, Izmir (Turkey); Broekmans, Maarten A.T.M. [Geological Survey of Norway, Dept. of Mineral Characterization, N-7491 Trondheim (Norway); Kuehnel, Radko [Burgemeester Merkusstraat 5, 2645 NJ, Delfgauw (Netherlands)

2009-07-15T23:59:59.000Z

236

Method of extracting coal from a coal refuse pile  

DOE Patents (OSTI)

A method of extracting coal from a coal refuse pile comprises soaking the coal refuse pile with an aqueous alkali solution and distributing an oxygen-containing gas throughout the coal refuse pile for a time period sufficient to effect oxidation of coal contained in the coal refuse pile. The method further comprises leaching the coal refuse pile with an aqueous alkali solution to solubilize and extract the oxidized coal as alkali salts of humic acids and collecting the resulting solution containing the alkali salts of humic acids. Calcium hydroxide may be added to the solution of alkali salts of humic acid to form precipitated humates useable as a low-ash, low-sulfur solid fuel.

Yavorsky, Paul M. (Monongahela, PA)

1991-01-01T23:59:59.000Z

237

A MOLTEN SALT NATURAL CONVECTION REACTOR SYSTEM  

SciTech Connect

Fuel-salt volumes external to the core of a molten-salt reactor are calculated for a system in which the fuel salt circulates through the core and primary exchanger by free convection. In the calculation of these volumes, the exchanger heights above the core top range from 5 to 20 ft. Coolants considered for the primary exchanger are a second molten salt and helium. External fuel holdup is found to be the same with either coolant. Two sets of terminal temperatures are selected for the helium. The first combination permits steam generation at 850 psia, 900 deg F. The second set is selected for a closed gas turbine cycle with an 1100 deg F turbine inlet temperature. Specific power (thermal kw/kg 235) is found to be about 900 Mv/kg, based on initial, clean conditions and a 60 Mw (thermal) output. A specific power of 1275 kw/kg is estimated for a forced convection system of the same rating. (auth)

Romie, F.E.; Kinyon, B.W.

1958-02-01T23:59:59.000Z

238

Salt repository project closeout status report  

SciTech Connect

This report provides an overview of the scope and status of the US Department of Energy (DOE`s) Salt Repository Project (SRP) at the time when the project was terminated by the Nuclear Waste Policy Amendments Act of 1987. The report reviews the 10-year program of siting a geologic repository for high-level nuclear waste in rock salt formations. Its purpose is to aid persons interested in the information developed during the course of this effort. Each area is briefly described and the major items of information are noted. This report, the three salt Environmental Assessments, and the Site Characterization Plan are the suggested starting points for any search of the literature and information developed by the program participants. Prior to termination, DOE was preparing to characterize three candidate sites for the first mined geologic repository for the permanent disposal of high-level nuclear waste. The sites were in Nevada, a site in volcanic tuff; Texas, a site in bedded salt (halite); and Washington, a site in basalt. These sites, identified by the screening process described in Chapter 3, were selected from the nine potentially acceptable sites shown on Figure I-1. These sites were identified in accordance with provisions of the Nuclear Waste Policy Act of 1982. 196 refs., 21 figs., 11 tabs.

1988-06-01T23:59:59.000Z

239

Accelerators for Subcritical Molten-Salt Reactors  

SciTech Connect

Accelerator parameters for subcritical reactors have usually been based on using solid nuclear fuel much like that used in all operating critical reactors as well as the thorium burning accelerator-driven energy amplifier proposed by Rubbia et al. An attractive alternative reactor design that used molten salt fuel was experimentally studied at ORNL in the 1960s, where a critical molten salt reactor was successfully operated using enriched U235 or U233 tetrafluoride fuels. These experiments give confidence that an accelerator-driven subcritical molten salt reactor will work better than conventional reactors, having better efficiency due to their higher operating temperature, having the inherent safety of subcritical operation, and having constant purging of volatile radioactive elements to eliminate their accumulation and potential accidental release in dangerous amounts. Moreover, the requirements to drive a molten salt reactor can be considerably relaxed compared to a solid fuel reactor, especially regarding accelerator reliability and spallation neutron targetry, to the point that much of the required technology exists today. It is proposed that Project-X be developed into a prototype commercial machine to produce energy for the world by, for example, burning thorium in India and nuclear waste from conventional reactors in the USA.

Johnson, Roland (Muons, Inc.)

2011-08-03T23:59:59.000Z

240

Internal Wave Overturns Produced by Salt Fingers  

Science Conference Proceedings (OSTI)

The salt finger fluxes obtained in small-domain direct numerical simulations (DNSs) are used to parameterize the fluxes in a larger domain that resolves internal gravity waves. For the case in which the molecular diffusivity ratio ? = KS/KT < 1 ...

Melvin E. Stern; Julian A. Simeonov

2002-12-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Energy Efficient Buildings, Salt Lake County, Utah  

SciTech Connect

Executive Summary Salt Lake County's Solar Photovoltaic Project - an unprecedented public/private partnership Salt Lake County is pleased to announce the completion of its unprecedented solar photovoltaic (PV) installation on the Calvin R. Rampton Salt Palace Convention Center. This 1.65 MW installation will be one the largest solar roof top installations in the country and will more than double the current installed solar capacity in the state of Utah. Construction is complete and the system will be operational in May 2012. The County has accomplished this project using a Power Purchase Agreement (PPA) financing model. In a PPA model a third-party solar developer will finance, develop, own, operate, and maintain the solar array. Salt Lake County will lease its roof, and purchase the power from this third-party under a long-term Power Purchase Agreement contract. In fact, this will be one of the first projects in the state of Utah to take advantage of the recent (March 2010) legislation which makes PPA models possible for projects of this type. In addition to utilizing a PPA, this solar project will employ public and private capital, Energy Efficiency and Conservation Block Grants (EECBG), and public/private subsidized bonds that are able to work together efficiently because of the recent stimulus bill. The project also makes use of recent changes to federal tax rules, and the recent re-awakening of private capital markets that make a significant public-private partnership possible. This is an extremely innovative project, and will mark the first time that all of these incentives (EECBG grants, Qualified Energy Conservation Bonds, New Markets tax credits, investment tax credits, public and private funds) have been packaged into one project. All of Salt Lake County's research documents and studies, agreements, and technical information is available to the public. In addition, the County has already shared a variety of information with the public through webinars, site tours, presentations, and written correspondence.

Barnett, Kimberly

2012-04-30T23:59:59.000Z

242

The Salt Finger Experiments of Jevons (1857) and Rayleigh (1880)  

Science Conference Proceedings (OSTI)

Over a century before Melvin Stern discovered salt fingers, W. Stanley Jevons performed the first salt finger experiment in an attempt to model cirrus clouds. Remarkably, he seemed to realize that a more rapid diffusion of heat relative to solute ...

Raymond W. Schmitt

1995-01-01T23:59:59.000Z

243

Salt Wells, Eight Mile Flat | Open Energy Information  

Open Energy Info (EERE)

Salt Wells, Eight Mile Flat Salt Wells, Eight Mile Flat Jump to: navigation, search OpenEI Reference LibraryAdd to library Web Site: Salt Wells, Eight Mile Flat Abstract Abstract unavailable. Author Nevada Bureau of Mines and Geology Published Online Nevada Encyclopedia, 2009 DOI Not Provided Check for DOI availability: http://crossref.org Online Internet link for Salt Wells, Eight Mile Flat Citation Nevada Bureau of Mines and Geology. Salt Wells, Eight Mile Flat [Internet]. 2009. Online Nevada Encyclopedia. [updated 2009/03/24;cited 2013/08/07]. Available from: http://www.onlinenevada.org/articles/salt-wells-eight-mile-flat Related Geothermal Exploration Activities Activities (1) Areas (1) Regions (0) Development Wells At Salt Wells Area (Nevada Bureau of Mines and Geology, 2009) Salt Wells Geothermal Area

244

Brine Migration Experimental Studies for Salt Repositories | Department of  

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

Brine Migration Experimental Studies for Salt Repositories Brine Migration Experimental Studies for Salt Repositories Brine Migration Experimental Studies for Salt Repositories Experiments were used to examine water content in Permian salt samples (Salado Formation) collected from the WIPP site. The profile of water release and movement is recognized as a function of temperature from 30 to 275 oC using classical gravimetric methods to measure weight loss as a result of heating. The amount of water released from heating the salt was found to be correlated with the salts accessory mineral content (clay, other secondary minerals lost up to 3 wt % while pure halite salt lost less than 0.5 wt % water). Water released from salt at lower temperature was reversible and is attributed to clay hydration and dehydration processes. The analysis

245

Brine Migration Experimental Studies for Salt Repositories | Department of  

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

Brine Migration Experimental Studies for Salt Repositories Brine Migration Experimental Studies for Salt Repositories Brine Migration Experimental Studies for Salt Repositories Experiments were used to examine water content in Permian salt samples (Salado Formation) collected from the WIPP site. The profile of water release and movement is recognized as a function of temperature from 30 to 275 oC using classical gravimetric methods to measure weight loss as a result of heating. The amount of water released from heating the salt was found to be correlated with the salts accessory mineral content (clay, other secondary minerals lost up to 3 wt % while pure halite salt lost less than 0.5 wt % water). Water released from salt at lower temperature was reversible and is attributed to clay hydration and dehydration processes. The analysis

246

SunShot Initiative: Advanced Nitrate Salt Central Receiver Power...  

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

Advanced Nitrate Salt Central Receiver Power Plant to someone by E-mail Share SunShot Initiative: Advanced Nitrate Salt Central Receiver Power Plant on Facebook Tweet about SunShot...

247

Similarity measures for spectral discrimination of salt-affected soils  

Science Conference Proceedings (OSTI)

This paper illustrates a pilot study designed to examine the spectral response of soils due to salt variations. The aim of the study includes determining whether salt-affected soils can be discriminated based on their spectral characteristics, by establishing ...

J. Farifteh; F. van der Meer; E. J. M. Carranza

2007-11-01T23:59:59.000Z

248

DOE Issues Salt Waste Determination for the Savannah River Site...  

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

Salt Waste Determination for the Savannah River Site DOE Issues Salt Waste Determination for the Savannah River Site January 18, 2006 - 10:49am Addthis WASHINGTON, DC - The U.S....

249

Colloidal stability of magnetic nanoparticles in molten salts  

E-Print Network (OSTI)

Molten salts are important heat transfer fluids used in nuclear, solar and other high temperature engineering systems. Dispersing nanoparticles in molten salts can enhance the heat transfer capabilities of the fluid. High ...

Somani, Vaibhav (Vaibhav Basantkumar)

2010-01-01T23:59:59.000Z

250

Removal of uranium and salt from the Molten Salt Reactor Experiment  

SciTech Connect

In 1994, migration of {sup 233}U was discovered to have occurred at the Molten Salt Reactor Experiment (MSRE) at Oak Ridge National Laboratory (ORNL). This paper describes the actions now underway to remove uranium from the off-gas piping and the charcoal bed, to remove and stabilize the salts, and to convert the uranium to a stable oxide for long-term storage.

Peretz, F.J.; Rushton, J.E.; Faulkner, R.L.; Walker, K.L.; Del Cul, G.D.

1998-06-01T23:59:59.000Z

251

Studies on the Effects of Inorganic Salts on Biochemical Treatment ...  

Science Conference Proceedings (OSTI)

Effects of two inorganic salts (sodium chloride and sodium sulphate) on biochemical ... Numerical Investigation of Heat Transfer Characteristics in Microwave ...

252

Method for preparing salt solutions having desired properties  

DOE Patents (OSTI)

The specification discloses a method for preparing salt solutions which exhibit desired thermodynamic properties. The method enables prediction of the value of the thermodynamic properties for single and multiple salt solutions over a wide range of conditions from activity data and constants which are independent of concentration and temperature. A particular application of the invention is in the control of salt solutions in a process to provide a salt solution which exhibits the desired properties.

Ally, Moonis R. (Oak Ridge, TN); Braunstein, Jerry (Clinton, TN)

1994-01-01T23:59:59.000Z

253

Molten Salt Heat Transfer Fluid (HTF) - Energy Innovation Portal  

Solar Thermal Industrial Technologies Energy Storage Molten Salt Heat Transfer Fluid (HTF) Sandia National Laboratories. Contact SNL About This ...

254

CO2 Emission Reduction through Innovative Molten Salt Electrolysis ...  

Science Conference Proceedings (OSTI)

Electrochemical metallurgy especially through high temperature molten salt electrolysis with renewable electricity stands for a great opportunity for producing

255

Effect of Sodium Carboxymethyl Celluloses on Water-catalyzed Self-degradation of 200-degree C-heated Alkali-Activated Cement  

SciTech Connect

We investigated the usefulness of sodium carboxymethyl celluloses (CMC) in promoting self-degradation of 200°C-heated sodium silicate-activated slag/Class C fly ash cementitious material after contact with water. CMC emitted two major volatile compounds, CO2 and acetic acid, creating a porous structure in cement. CMC also reacted with NaOH from sodium silicate to form three water-insensitive solid reaction products, disodium glycolate salt, sodium glucosidic salt, and sodium bicarbonate. Other water-sensitive solid reaction products, such as sodium polysilicate and sodium carbonate, were derived from hydrolysates of sodium silicate. Dissolution of these products upon contact with water generated heat that promoted cement’s self-degradation. Thus, CMC of high molecular weight rendered two important features to the water-catalyzed self-degradation of heated cement: One was the high heat energy generated in exothermic reactions in cement; the other was the introduction of extensive porosity into cement.

Sugama T.; Pyatina, T.

2012-05-01T23:59:59.000Z

256

SOLUTION MINING IN SALT DOMES OF THE GULF COAST EMBAYMENT  

Science Conference Proceedings (OSTI)

Following a description of salt resources in the salt domes of the gulf coast embayment, mining, particularly solution mining, is described. A scenario is constructed which could lead to release of radioactive waste stored in a salt dome via inadvertent solution mining and the consequences of this scenario are analyzed.

Griswold, G. B.

1981-02-01T23:59:59.000Z

257

Electrokinetic behavior of fluoride salts as explained from water structure considerations  

Science Conference Proceedings (OSTI)

Unlike the other silver halides, silver fluoride is positively charged in its saturated solution as determined by nonequilibrium electrophoresis measurements. In the absence of surface hydrolysis reactions, other fluoride salts (LiF, CaF{sub 2}, and MgF{sub 2}) also are positively charged in their saturation solutions. Furthermore, the electrokinetic behavior of these fluoride salts is rather insensitive to the fluoride ion activity in neutral or acidic solutions, and reversal of the sign of the surface charge by fluoride addition is not possible. Based on FTIR transmission spectra to describe the water structure of ionic solutions, in situ FTIR/internal reflection spectroscopy (FTIR/IRS) has been used to spectroscopically characterize interfacial water at fluoride salt surfaces. The experimental spectra were examined by consideration of the O-H stretching region (3,000--3,800 cm{sup {minus}1}) associated with the vibrational spectra of interfacial water. These results reveal a unique hydration state for fluorides and explain the anomalous electrokinetic behavior of fluoride salts such as LiF, CaF{sub 2}, and MgF{sub 2}, which show an unexpected insensitivity to the fluoride ion concentration in solution. It appears that this insensitivity is due to the formation of strong hydrogen bonding of the fluoride ions with water molecules. This hydration state prevents the accommodation of excess fluoride ions at surface lattice sites and accounts for the observed electrokinetic behavior.

Hu, Y.; Lu, Y.; Veeramasuneni, S.; Miller, J.D. [Univ. of Utah, Salt Lake City, UT (United States). Dept. of Metallurgical Engineering

1997-06-01T23:59:59.000Z

258

Salt River Project | Open Energy Information  

Open Energy Info (EERE)

Project Project Jump to: navigation, search Name Salt River Project Place Tempe, Arizona Utility Id 16572 Utility Location Yes Ownership P NERC Location WECC NERC WECC Yes Operates Generating Plant Yes Activity Generation Yes Activity Transmission Yes Activity Buying Transmission Yes Activity Distribution Yes Activity Wholesale Marketing Yes Activity Bundled Services Yes Alt Fuel Vehicle Yes Alt Fuel Vehicle2 Yes References EIA Form EIA-861 Final Data File for 2010 - File1_a[1] SGIC[2] Energy Information Administration Form 826[3] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Salt River Project Smart Grid Project was awarded $56,859,359 Recovery Act Funding with a total project value of $114,003,719.

259

Molten salts database for energy applications  

E-Print Network (OSTI)

The growing interest in energy applications of molten salts is justified by several of their properties. Their possibilities of usage as a coolant, heat transfer fluid or heat storage substrate, require thermo-hydrodynamic refined calculations. Many researchers are using simulation techniques, such as Computational Fluid Dynamics (CFD) for their projects or conceptual designs. The aim of this work is providing a review of basic properties (density, viscosity, thermal conductivity and heat capacity) of the most common and referred salt mixtures. After checking data, tabulated and graphical outputs are given in order to offer the most suitable available values to be used as input parameters for other calculations or simulations. The reviewed values show a general scattering in characterization, mainly in thermal properties. This disagreement suggests that, in several cases, new studies must be started (and even new measurement techniques should be developed) to obtain accurate values.

Serrano-López, Roberto; Cuesta-López, Santiago

2013-01-01T23:59:59.000Z

260

Salt River Electric - Residential Energy Efficiency Rebate Program |  

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

Salt River Electric - Residential Energy Efficiency Rebate Program Salt River Electric - Residential Energy Efficiency Rebate Program Salt River Electric - Residential Energy Efficiency Rebate Program < Back Eligibility Residential Savings Category Home Weatherization Commercial Weatherization Sealing Your Home Heating & Cooling Construction Commercial Heating & Cooling Design & Remodeling Other Ventilation Heat Pumps Program Info State Kentucky Program Type Utility Rebate Program Rebate Amount Varies by technology Provider Salt River Electric Cooperative Salt River Electric serves as the rural electric provider in Kentucky's Bullitt, Nelson, Spencer, and Washington counties. Residential customers are eligible for a variety of cash incentives for energy efficiency. The Touchstone Energy Home Program provides a rebate of up to $250 to customers

Note: This page contains sample records for the topic "acids alkalies salts" 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

Energy Efficient Buildings, Salt Lake County, Utah  

DOE Green Energy (OSTI)

Salt Lake County is pleased to announce the completion of its unprecedented solar photovoltaic (PV) installation on the Calvin R. Rampton Salt Palace Convention Center. This 1.65 MW installation will be one the largest solar roof top installations in the country and will more than double the current installed solar capacity in the state of Utah. Construction is complete and the system will be operational in May 2012. The County has accomplished this project using a Power Purchase Agreement (PPA) financing model. In a PPA model a third-party solar developer will finance, develop, own, operate, and maintain the solar array. Salt Lake County will lease its roof, and purchase the power from this third-party under a long-term Power Purchase Agreement contract. In fact, this will be one of the first projects in the state of Utah to take advantage of the recent (March 2010) legislation which makes PPA models possible for projects of this type. In addition to utilizing a PPA, this solar project will employ public and private capital, Energy Efficiency and Conservation Block Grants (EECBG), and public/private subsidized bonds that are able to work together efficiently because of the recent stimulus bill. The project also makes use of recent changes to federal tax rules, and the recent re-awakening of private capital markets that make a significant public-private partnership possible. This is an extremely innovative project, and will mark the first time that all of these incentives (EECBG grants, Qualified Energy Conservation Bonds, New Markets tax credits, investment tax credits, public and private funds) have been packaged into one project. All of Salt Lake County's research documents and studies, agreements, and technical information is available to the public. In addition, the County has already shared a variety of information with the public through webinars, site tours, presentations, and written correspondence.

Barnett, Kimberly

2012-04-30T23:59:59.000Z

262

Molten salt battery having inorganic paper separator  

DOE Patents (OSTI)

A high temperature secondary battery comprises an anode containing lithium, a cathode containing a chalcogen or chalcogenide, a molten salt electrolyte containing lithium ions, and a separator comprising a porous sheet comprising a homogenous mixture of 2-20 wt.% chrysotile asbestos fibers and the remainder inorganic material non-reactive with the battery components. The non-reactive material is present as fibers, powder, or a fiber-powder mixture.

Walker, Jr., Robert D. (Gainesville, FL)

1977-01-01T23:59:59.000Z

263

Effect of silicate modulus and metakaolin incorporation on the carbonation of alkali silicate-activated slags  

SciTech Connect

Accelerated carbonation is induced in pastes and mortars produced from alkali silicate-activated granulated blast furnace slag (GBFS)-metakaolin (MK) blends, by exposure to CO{sub 2}-rich gas atmospheres. Uncarbonated specimens show compressive strengths of up to 63 MPa after 28 days of curing when GBFS is used as the sole binder, and this decreases by 40-50% upon complete carbonation. The final strength of carbonated samples is largely independent of the extent of metakaolin incorporation up to 20%. Increasing the metakaolin content of the binder leads to a reduction in mechanical strength, more rapid carbonation, and an increase in capillary sorptivity. A higher susceptibility to carbonation is identified when activation is carried out with a lower solution modulus (SiO{sub 2}/Na{sub 2}O ratio) in metakaolin-free samples, but this trend is reversed when metakaolin is added due to the formation of secondary aluminosilicate phases. High-energy synchrotron X-ray diffractometry of uncarbonated paste samples shows that the main reaction products in alkali-activated GBFS/MK blends are C-S-H gels, and aluminosilicates with a zeolitic (gismondine) structure. The main crystalline carbonation products are calcite in all samples and trona only in samples containing no metakaolin, with carbonation taking place in the C-S-H gels of all samples, and involving the free Na{sup +} present in the pore solution of the metakaolin-free samples. Samples containing metakaolin do not appear to have the same availability of Na{sup +} for carbonation, indicating that this is more effectively bound in the presence of a secondary aluminosilicate gel phase. It is clear that claims of exceptional carbonation resistance in alkali-activated binders are not universally true, but by developing a fuller mechanistic understanding of this process, it will certainly be possible to improve performance in this area.

Bernal, Susan A., E-mail: susana.bernal@gmail.co [Materials Engineering Department, Composite Materials Group, CENM, Universidad del Valle, Cali (Colombia); Mejia de Gutierrez, Ruby [Materials Engineering Department, Composite Materials Group, CENM, Universidad del Valle, Cali (Colombia); Provis, John L., E-mail: jprovis@unimelb.edu.a [Department of Chemical and Biomolecular Engineering, University of Melbourne, Victoria 3010 (Australia); Rose, Volker [Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439 (United States)

2010-06-15T23:59:59.000Z

264

Reference repository design concept for bedded salt  

Science Conference Proceedings (OSTI)

A reference design concept is presented for the subsurface portions of a nuclear waste repository in bedded salt. General geologic, geotechnical, hydrologic and geochemical data as well as descriptions of the physical systems are provided for use on generic analyses of the pre- and post-sealing performance of repositories in this geologic medium. The geology of bedded salt deposits and the regional and repository horizon stratigraphy are discussed. Structural features of salt beds including discontinuities and dissolution features are presented and their effect on repository performance is discussed. Seismic hazards and the potential effects of earthquakes on underground repositories are presented. The effect on structural stability and worker safety during construction from hydrocarbon and inorganic gases is described. Geohydrologic considerations including regional hydrology, repository scale hydrology and several hydrological failure modes are presented in detail as well as the hydrological considerations that effect repository design. Operational phase performance is discussed with respect to operations, ventilation system, shaft conveyances, waste handling and retrieval systems and receival rates of nuclear waste. Performance analysis of the post sealing period of a nuclear repository is discussed, and parameters to be used in such an analysis are presented along with regulatory constraints. Some judgements are made regarding hydrologic failure scenarios. Finally, the design and licensing process, consistent with the current licensing procedure is described in a format that can be easily understood.

Carpenter, D.W.; Martin, R.W.

1980-10-08T23:59:59.000Z

265

Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Granular  

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

Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Granular Salt Consolidation, Constitutive Model and Micromechanics Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Granular Salt Consolidation, Constitutive Model and Micromechanics The report addresses granular salt reconsolidation from three vantage points: laboratory testing, modeling, and petrofabrics. The experimental data 1) provide greater insight and understanding into the role of elevated temperature and pressure regimes on physical properties of reconsolidated crushed salt, 2) can supplement an existing database used to develop a reconsolidation constitutive model and 3) provide data for model evaluation. The constitutive model accounts for the effects of moisture through pressure solution and dislocation creep, with both terms dependent

266

Polymeric salt bridges for conducting electric current in microfluidic devices  

DOE Patents (OSTI)

A "cast-in-place" monolithic microporous polymer salt bridge for conducting electrical current in microfluidic devices, and methods for manufacture thereof is disclosed. Polymeric salt bridges are formed in place in capillaries or microchannels. Formulations are prepared with monomer, suitable cross-linkers, solvent, and a thermal or radiation responsive initiator. The formulation is placed in a desired location and then suitable radiation such as UV light is used to polymerize the salt bridge within a desired structural location. Embodiments are provided wherein the polymeric salt bridges have sufficient porosity to allow ionic migration without bulk flow of solvents therethrough. The salt bridges form barriers that seal against fluid pressures in excess of 5000 pounds per square inch. The salt bridges can be formulated for carriage of suitable amperage at a desired voltage, and thus microfluidic devices using such salt bridges can be specifically constructed to meet selected analytical requirements.

Shepodd, Timothy J. (Livermore, CA); Tichenor, Mark S. (San Diego, CA); Artau, Alexander (Humacao, PR)

2009-11-17T23:59:59.000Z

267

Pyrochemical process for extracting plutonium from an electrolyte salt  

DOE Patents (OSTI)

A pyrochemical process for extracting plutonium from a plutonium-bearing salt is disclosed. The process is particularly useful in the recovery of plutonium from electrolyte salts which are left over from the electrorefining of plutonium. In accordance with the process, the plutonium-bearing salt is melted and mixed with metallic calcium. The calcium reduces ionized plutonium in the salt to plutonium metal, and also causes metallic plutonium in the salt, which is typically present as finely dispersed metallic shot, to coalesce. The reduced and coalesced plutonium separates out on the bottom of the reaction vessel as a separate metallic phase which is readily separable from the overlying salt upon cooling of the mixture. Yields of plutonium are typically on the order of 95%. The stripped salt is virtually free of plutonium and may be discarded to low-level waste storage.

Mullins, Lawrence J. (Los Alamos, NM); Christensen, Dana C. (Los Alamos, NM)

1984-01-01T23:59:59.000Z

268

Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Granular  

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

Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Granular Salt Consolidation, Constitutive Model and Micromechanics Coupled Thermal-Hydrological-Mechanical Processes in Salt, Hot Granular Salt Consolidation, Constitutive Model and Micromechanics The report addresses granular salt reconsolidation from three vantage points: laboratory testing, modeling, and petrofabrics. The experimental data 1) provide greater insight and understanding into the role of elevated temperature and pressure regimes on physical properties of reconsolidated crushed salt, 2) can supplement an existing database used to develop a reconsolidation constitutive model and 3) provide data for model evaluation. The constitutive model accounts for the effects of moisture through pressure solution and dislocation creep, with both terms dependent

269

Aksaray And Ecemis Faults - Diapiric Salt Relationships- Relevance To The  

Open Energy Info (EERE)

Aksaray And Ecemis Faults - Diapiric Salt Relationships- Relevance To The Aksaray And Ecemis Faults - Diapiric Salt Relationships- Relevance To The Hydrocarbon Exploration In The Tuz Golu (Salt Lake) Basin, Central Anatolia, Turkey Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Aksaray And Ecemis Faults - Diapiric Salt Relationships- Relevance To The Hydrocarbon Exploration In The Tuz Golu (Salt Lake) Basin, Central Anatolia, Turkey Details Activities (0) Areas (0) Regions (0) Abstract: Due to activitiy of the Aksaray and Ecemis Faults, volcanic intrusion and westward movement of the Anatolian plate, diapiric salt structures were occurred in the Tuz Golu (Salt Lake) basin in central Anatolia, Turkey. With the collisions of the Arabian and Anatolian plates during the late Cretaceous and Miocene times, prominent ophiolitic

270

WIPP Shares Expertise with Salt Club Members | Department of Energy  

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

Shares Expertise with Salt Club Members Shares Expertise with Salt Club Members WIPP Shares Expertise with Salt Club Members November 26, 2013 - 12:00pm Addthis Carlsbad Field Office’s Abe Van Luik, third from right, examines rock salt taken from the Morsleben mine in Germany. Carlsbad Field Office's Abe Van Luik, third from right, examines rock salt taken from the Morsleben mine in Germany. CARLSBAD, N.M. - EM's Carlsbad Field Office (CBFO) participated in the second meeting of the Nuclear Energy Agency's (NEA) Salt Club and the 4th U.S.-German Workshop on Salt Repository Research, Design & Operation in Berlin. CBFO, which has responsibility for the Waste Isolation Pilot Plant (WIPP) and the National Transuranic (TRU) Program, was represented by International Programs and Policy Advisor Dr. Abe Van Luik.

271

Salt Waste Contractor Reaches Contract Milestone | Department of Energy  

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

Salt Waste Contractor Reaches Contract Milestone Salt Waste Contractor Reaches Contract Milestone Salt Waste Contractor Reaches Contract Milestone April 29, 2013 - 12:00pm Addthis Robert Brown, SRR tank farm operator, performs daily inspections of a salt disposition process facility. The inspections and improvement upgrades have resulted in continued successful operations. Robert Brown, SRR tank farm operator, performs daily inspections of a salt disposition process facility. The inspections and improvement upgrades have resulted in continued successful operations. AIKEN, S.C. - The liquid waste cleanup contractor for the EM program at the Savannah River Site (SRS) recently surpassed a 2013 contract milestone by processing more than 600,000 gallons of salt waste. Savannah River Remediation (SRR) salt disposition process facilities

272

Cementitious Stabilization of Mixed Wastes with High Salt Loadings  

SciTech Connect

Salt loadings approaching 50 wt % were tolerated in cementitious waste forms that still met leach and strength criteria, addressing a Technology Deficiency of low salt loadings previously identified by the Mixed Waste Focus Area. A statistical design quantified the effect of different stabilizing ingredients and salt loading on performance at lower loadings, allowing selection of the more effective ingredients for studying the higher salt loadings. In general, the final waste form needed to consist of 25 wt % of the dry stabilizing ingredients to meet the criteria used and 25 wt % water to form a workable paste, leaving 50 wt % for waste solids. The salt loading depends on the salt content of the waste solids but could be as high as 50 wt % if all the waste solids are salt.

Spence, R.D.; Burgess, M.W.; Fedorov, V.V.; Downing, D.J.

1999-04-01T23:59:59.000Z

273

Pyrochemical process for extracting plutonium from an electrolyte salt  

DOE Patents (OSTI)

A pyrochemical process for extracting plutonium from a plutonium-bearing salt is disclosed. The process is particularly useful in the recovery of plutonium for electrolyte salts which are left over from the electrorefining of plutonium. In accordance with the process, the plutonium-bearing salt is melted and mixed with metallic calcium. The calcium reduces ionized plutonium in the salt to plutonium metal, and also causes metallic plutonium in the salt, which is typically present as finely dispersed metallic shot, to coalesce. The reduced and coalesced plutonium separates out on the bottom of the reaction vessel as a separate metallic phase which is readily separable from the overlying salt upon cooling of the mixture. Yields of plutonium are typically on the order of 95%. The stripped salt is virtually free of plutonium and may be discarded to low-level waste storage.

Mullins, L.J.; Christensen, D.C.

1982-09-20T23:59:59.000Z

274

DuraLith Alkali-Aluminosilicate Geopolymer Waste Form Testing for Hanford Secondary Waste  

SciTech Connect

The primary objective of the work reported here was to develop additional information regarding the DuraLith alkali aluminosilicate geopolymer as a waste form for liquid secondary waste to support selection of a final waste form for the Hanford Tank Waste Treatment and Immobilization Plant secondary liquid wastes to be disposed in the Integrated Disposal Facility on the Hanford Site. Testing focused on optimizing waste loading, improving waste form performance, and evaluating the robustness of the waste form with respect to waste variability.

Gong, W. L.; Lutz, Werner; Pegg, Ian L.

2011-07-21T23:59:59.000Z

275

Amine derivatives of thio-bis-lactone acids in combination with coadditive hydrocarbons are flow improvers for middle distillate fuel oils  

Science Conference Proceedings (OSTI)

Amine salts, amino acids, amino acid salts bis-amides and imides of oil-soluble thio-bis-(C12-50 alkyl lactone acid), e.g. a secondary hydrogenated tallow amide of dithio-bis-(C16-c24 alkyl lactone carboxylic acid), are useful in combination with a coadditive hydrocarbon such as an amorphous hydrocarbon or a hydrogenated polybutadiene in improving the cold flow properties of distillate hydrocarbon oils.

Brois, S.J.; Feldman, N.; Gutierrez, A.

1981-02-17T23:59:59.000Z

276

High thermal energy storage density molten salts for parabolic trough solar power generation.  

E-Print Network (OSTI)

??New alkali nitrate-nitrite systems were developed by using thermodynamic modeling and the eutectic points were predicted based on the change of Gibbs energy of fusion.… (more)

Wang, Tao

2011-01-01T23:59:59.000Z

277

Investigation of anti-Relaxation coatings for alkali-metal vapor cells using surface science techniques  

SciTech Connect

Many technologies based on cells containing alkali-metal atomic vapor benefit from the use of antirelaxation surface coatings in order to preserve atomic spin polarization. In particular, paraffin has been used for this purpose for several decades and has been demonstrated to allow an atom to experience up to 10?000 collisions with the walls of its container without depolarizing, but the details of its operation remain poorly understood. We apply modern surface and bulk techniques to the study of paraffin coatings in order to characterize the properties that enable the effective preservation of alkali spin polarization. These methods include Fourier transform infrared spectroscopy, differential scanning calorimetry, atomic force microscopy, near-edge x-ray absorption fine structure spectroscopy, and x-ray photoelectron spectroscopy. We also compare the light-induced atomic desorption yields of several different paraffin materials. Experimental results include the determination that crystallinity of the coating material is unnecessary, and the detection of C=C double bonds present within a particular class of effective paraffin coatings. Further study should lead to the development of more robust paraffin antirelaxation coatings, as well as the design and synthesis of new classes of coating materials.

Seltzer, S. J.; Michalak, D. J.; Donaldson, M. H.; Balabas, M. V.; Barber, S. K.; Bernasek, S. L.; Bouchiat, M.-A.; Hexemer, A.; Hibberd, A. M.; Jackson Kimball, D. F.; Jaye, C.; Karaulanov, T.; Narducci, F. A.; Rangwala, S. A.; Robinson, H. G.; Shmakov, A. K.; Voronov, D. L.; Yashchuk, V. V.; Pines, A.; Budker, D.

2010-10-11T23:59:59.000Z

278

An Overview of Liquid Fluoride Salt Heat Transport Technology  

SciTech Connect

Liquid fluoride salts are a leading candidate heat transport medium for high-temperature applications. This report provides an overview of the current status of liquid salt heat transport technology. The report includes a high-level, parametric evaluation of liquid fluoride salt heat transport loop performance to allow intercomparisons between heat-transport fluid options as well as providing an overview of the properties and requirements for a representative loop. Much of the information presented here derives from the earlier molten salt reactor program and a significant advantage of fluoride salts, as high temperature heat transport media is their consequent relative technological maturity. The report also includes a compilation of relevant thermophysical properties of useful heat transport fluoride salts. Fluoride salts are both thermally stable and with proper chemistry control can be relatively chemically inert. Fluoride salts can, however, be highly corrosive depending on the container materials selected, the salt chemistry, and the operating procedures used. The report also provides an overview of the state-of-the-art in reduction-oxidation chemistry control methodologies employed to minimize salt corrosion as well as providing a general discussion of heat transfer loop operational issues such as start-up procedures and freeze-up vulnerability.

Cetiner, Mustafa Sacit [ORNL; Holcomb, David Eugene [ORNL

2010-01-01T23:59:59.000Z

279

Salt disposal of heat-generating nuclear waste.  

SciTech Connect

This report summarizes the state of salt repository science, reviews many of the technical issues pertaining to disposal of heat-generating nuclear waste in salt, and proposes several avenues for future science-based activities to further the technical basis for disposal in salt. There are extensive salt formations in the forty-eight contiguous states, and many of them may be worthy of consideration for nuclear waste disposal. The United States has extensive experience in salt repository sciences, including an operating facility for disposal of transuranic wastes. The scientific background for salt disposal including laboratory and field tests at ambient and elevated temperature, principles of salt behavior, potential for fracture damage and its mitigation, seal systems, chemical conditions, advanced modeling capabilities and near-future developments, performance assessment processes, and international collaboration are all discussed. The discussion of salt disposal issues is brought current, including a summary of recent international workshops dedicated to high-level waste disposal in salt. Lessons learned from Sandia National Laboratories' experience on the Waste Isolation Pilot Plant and the Yucca Mountain Project as well as related salt experience with the Strategic Petroleum Reserve are applied in this assessment. Disposal of heat-generating nuclear waste in a suitable salt formation is attractive because the material is essentially impermeable, self-sealing, and thermally conductive. Conditions are chemically beneficial, and a significant experience base exists in understanding this environment. Within the period of institutional control, overburden pressure will seal fractures and provide a repository setting that limits radionuclide movement. A salt repository could potentially achieve total containment, with no releases to the environment in undisturbed scenarios for as long as the region is geologically stable. Much of the experience gained from United States repository development, such as seal system design, coupled process simulation, and application of performance assessment methodology, helps define a clear strategy for a heat-generating nuclear waste repository in salt.

Leigh, Christi D. (Sandia National Laboratories, Carlsbad, NM); Hansen, Francis D.

2011-01-01T23:59:59.000Z

280

Steam Reforming Technology Demonstration for Conversion of DOE Sodium-Bearing Tank Wastes at Idaho National Laboratory into a Leach-Resistant Alkali Aluminosilicate Waste Form  

Science Conference Proceedings (OSTI)

The patented THOR{sup R} fluidized-bed steam reforming (FBSR) technology was selected by the U.S. Department of Energy (DOE) for treatment of sodium-bearing waste (SBW) in the Integrated Waste Treatment Unit (IWTU), currently under construction at the Idaho National Laboratory (INL) Site.1 SBW is an acidic waste created primarily from cleanup of the fuel reprocessing equipment at the Idaho Nuclear Technology and Engineering Center (INTEC) at the INL. The SBW contains high concentrations of nitric acid, and alkali and aluminum nitrates, along with many other inorganic compounds, including substantial levels of radionuclides. As part of the implementation of the THOR{sup R} process at INTEC, an engineering-scale technology demonstration (ESTD) was conducted using a specially designed pilot plant located at Hazen Research, Inc. in Golden Colorado. This ESTD confirmed the efficacy of the THOR{sup R} FBSR process to convert the SBW into a granular carbonate-based waste form suitable for disposal at the Waste Isolation Pilot Plant (WIPP). DOE authorized, as a risk reduction measure, the performance of an additional ESTD to demonstrate the production of an insoluble mineralized product, in the event that an alternate disposition path is required. The additional ESTD was conducted at the Hazen Research facility using the THOR{sup R} process and the same SBW simulant employed previously. An alkali aluminosilicate mineral product was produced that exhibited excellent leach resistance and chemical durability. The demonstration established general system operating parameters for a full-scale facility; provided process off-gas data that confirmed operation within regulatory limits; determined that the mineralized product exhibits superior leach resistance and durability, compared to Environmental Assessment (EA) and Low-activity Reference Material (LRM) glasses, as indicated by the Product Consistency Test (PCT); ascertained that Cs and Re (a surrogate for Tc) were non-volatile and were retained in the mineral product; and showed that heavy metals were converted into mineral forms that were not leachable, as determined by the Toxicity Characteristic Leaching Procedure (TCLP) test. (authors)

Ryan, K.; Bradley Mason, J.; Evans, B.; Vora, V. [THOR Treatment Technologies, LLC, Aiken, SC (United States); Olson, A. [CH2M-WG Idaho, LLC, Idaho Falls, ID (United States)

2008-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Process for loading weak-acid ion exchange resin with uranium  

DOE Patents (OSTI)

A method for loading ion exchange resins is described. The process comprises contacting a weak acid cation exchange resin in the ammonium form with a uranyl fluoride salt solution.

Notz, Karl J. (Oak Ridge, TN)

1976-01-01T23:59:59.000Z

282

Supai salt karst features: Holbrook Basin, Arizona  

SciTech Connect

More than 300 sinkholes, fissures, depressions, and other collapse features occur along a 70 km (45 mi) dissolution front of the Permian Supai Formation, dipping northward into the Holbrook Basin, also called the Supai Salt Basin. The dissolution front is essentially coincident with the so-called Holbrook Anticline showing local dip reversal; rather than being of tectonic origin, this feature is likely a subsidence-induced monoclinal flexure caused by the northward migrating dissolution front. Three major areas are identified with distinctive attributes: (1) The Sinks, 10 km WNW of Snowflake, containing some 200 sinkholes up to 200 m diameter and 50 m depth, and joint controlled fissures and fissure-sinks; (2) Dry Lake Valley and contiguous areas containing large collapse fissures and sinkholes in jointed Coconino sandstone, some of which drained more than 50 acre-feet ({approximately}6 {times} 10{sup 4} m{sup 3}) of water overnight; and (3) the McCauley Sinks, a localized group of about 40 sinkholes 15 km SE of Winslow along Chevelon Creek, some showing essentially rectangular jointing in the surficial Coconino Formation. Similar salt karst features also occur between these three major areas. The range of features in Supai salt are distinctive, yet similar to those in other evaporate basins. The wide variety of dissolution/collapse features range in development from incipient surface expression to mature and old age. The features began forming at least by Pliocene time and continue to the present, with recent changes reportedly observed and verified on airphotos with 20 year repetition. The evaporate sequence along interstate transportation routes creates a strategic location for underground LPG storage in leached caverns. The existing 11 cavern field at Adamana is safely located about 25 miles away from the dissolution front, but further expansion initiatives will require thorough engineering evaluation.

Neal, J.T.

1994-12-31T23:59:59.000Z

283

Independent Oversight Assessment, Salt Waste Processing Facility Project -  

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

Salt Waste Processing Facility Salt Waste Processing Facility Project - January 2013 Independent Oversight Assessment, Salt Waste Processing Facility Project - January 2013 January 2013 Assessment of Nuclear Safety Culture at the Salt Waste Processing Facility Project The U.S. Department of Energy (DOE) Office of Enforcement and Oversight (Independent Oversight), within the Office of Health, Safety and Security (HSS), conducted an independent assessment of nuclear safety culture at the Salt Waste Processing Facility (SWPF) Project. The primary objective of the evaluation was to provide information regarding the status of the safety culture at the SWPF Project. The data collection phase of the assessment occurred during August - September 2012. Independent Oversight Assessment, Salt Waste Processing Facility Project -

284

Disposing of nuclear waste in a salt bed  

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

Disposing of nuclear waste in a salt bed Disposing of nuclear waste in a salt bed 1663 Los Alamos science and technology magazine Latest Issue:November 2013 All Issues » submit Disposing of nuclear waste in a salt bed Decades' worth of transuranic waste from Los Alamos is being laid to rest at the Waste Isolation Pilot Plant in southeastern New Mexico March 25, 2013 Disposing of nuclear waste in a salt bed Depending on the impurities embedded within it, the salt from WIPP can be anything from a reddish, relatively opaque rock to a clear crystal like the one shown here. Ordinary salt effectively seals transuranic waste in a long-term repository Transuranic waste, made of items such as lab coats and equipment that have been contaminated by radioactive elements heavier than uranium, is being shipped from the Los Alamos National Laboratory to a long-term storage

285

Genomic insights into salt adaptation in a desert poplar  

SciTech Connect

Despite the high economic and ecological importance of forests, our knowledge of the genomic evolution of trees under salt stress remains very limited. Here we report the genome sequence of the desert poplar, Populus euphratica, which exhibits high tolerance to sa lt stress. Its genome is very similar and collinear to that of the closely related mesophytic congener, P trichocarpa. However, we find that several gene families likely to be involved in tolerance to salt stress contain significantly more gene copies within the P euphratica lineage. Furthermore, genes showing evidence of positive selection are significantly enriched in functional categories related to salt stress. Some of these genes, and others within the same categories, are significantly upregulated under salt stress relative to their expression in another salt-sensitive poplar. Our results provide an important background for understanding tree adaptation to salt stress and facilitating the genetic improvement of cultivated poplars for saline soils.

Ma, Tao [Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences] [Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences; Wang, Junyi [BGI-Shenzhen, China] [BGI-Shenzhen, China; Zhou, Gongke [Key laboratory of Biofuels and Shandong Provincial Key Laboratory of Energy Genetics, Qingdao Instit] [Key laboratory of Biofuels and Shandong Provincial Key Laboratory of Energy Genetics, Qingdao Instit; Yue, Zhen [BGI-Shenzhen, China] [BGI-Shenzhen, China; Hu, Quanjun [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Chen, Yan [BGI-Shenzhen, China] [BGI-Shenzhen, China; Liu, Bingbing [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Qiu, Qiang [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Wang, Zhuo [BGI-Shenzhen, China] [BGI-Shenzhen, China; Zhang, Jian [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Wang, Kun [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Jaing, Dechun [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Gou, Caiyun [BGI-Shenzhen, China] [BGI-Shenzhen, China; Yu, Lili [BGI-Shenzhen, China] [BGI-Shenzhen, China; Zhan, Dongliang [BGI-Shenzhen, China] [BGI-Shenzhen, China; Zhou, Ran [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Luo, Wenchun [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Ma, Hui [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Yang, Yongzhi [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Pan, Shengkai [BGI-Shenzhen, China] [BGI-Shenzhen, China; Fang, Dongming [BGI-Shenzhen, China] [BGI-Shenzhen, China; Luo, Yadan [BGI-Shenzhen, China] [BGI-Shenzhen, China; Wang, Xia [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Wang, Gaini [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Wang, Juan [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Wang, Qian [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Lu, Xu [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Chen, Zhe [BGI-Shenzhen, China] [BGI-Shenzhen, China; Liu, Jinchao [BGI-Shenzhen, China] [BGI-Shenzhen, China; Lu, Yao [BGI-Shenzhen, China] [BGI-Shenzhen, China; Yin, Ye [BGI-Shenzhen, China] [BGI-Shenzhen, China; Yang, Huanming [BGI-Shenzhen, China] [BGI-Shenzhen, China; Abbott, Richard [School of Biology, University of St. Andrews, St andrews, Fife KY16 9TH, UK] [School of Biology, University of St. Andrews, St andrews, Fife KY16 9TH, UK; Wu, Yuxia [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Wan, Dongshi [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University; Li, Jia [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University] [State Key Laboratory of Grassland Agro-Ecosystem, Lanzhou University

2013-01-01T23:59:59.000Z

286

Integrated demonstration of molten salt oxidation with salt recycle for mixed waste treatment  

Science Conference Proceedings (OSTI)

Molten Salt Oxidation (MSO) is a thermal, nonflame process that has the inherent capability of completely destroying organic constituents of mixed wastes, hazardous wastes, and energetic materials while retaining inorganic and radioactive constituents in the salt. For this reason, MSO is considered a promising alternative to incineration for the treatment of a variety of organic wastes. Lawrence Livermore National Laboratory (LLNL) has prepared a facility and constructed an integrated pilot-scale MSO treatment system in which tests and demonstrations are performed under carefully controlled (experimental) conditions. The system consists of a MSO processor with dedicated off-gas treatment, a salt recycle system, feed preparation equipment, and equipment for preparing ceramic final waste forms. This integrated system was designed and engineered based on laboratory experience with a smaller engineering-scale reactor unit and extensive laboratory development on salt recycle and final forms preparation. In this paper we present design and engineering details of the system and discuss its capabilities as well as preliminary process demonstration data. A primary purpose of these demonstrations is identification of the most suitable waste streams and waste types for MSO treatment.

Hsu, P.C.

1997-11-01T23:59:59.000Z

287

Delivery system for molten salt oxidation of solid waste  

DOE Patents (OSTI)

The present invention is a delivery system for safety injecting solid waste particles, including mixed wastes, into a molten salt bath for destruction by the process of molten salt oxidation. The delivery system includes a feeder system and an injector that allow the solid waste stream to be accurately metered, evenly dispersed in the oxidant gas, and maintained at a temperature below incineration temperature while entering the molten salt reactor.

Brummond, William A. (Livermore, CA); Squire, Dwight V. (Livermore, CA); Robinson, Jeffrey A. (Manteca, CA); House, Palmer A. (Walnut Creek, CA)

2002-01-01T23:59:59.000Z

288

Columbus Salt Marsh Geothermal Area | Open Energy Information  

Open Energy Info (EERE)

Columbus Salt Marsh Geothermal Area Columbus Salt Marsh Geothermal Area (Redirected from Columbus Salt Marsh Area) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Geothermal Resource Area: Columbus Salt Marsh Geothermal Area Contents 1 Area Overview 2 History and Infrastructure 3 Regulatory and Environmental Issues 4 Exploration History 5 Well Field Description 6 Geology of the Area 7 Geofluid Geochemistry 8 NEPA-Related Analyses (0) 9 Exploration Activities (3) 10 References Area Overview Geothermal Area Profile Location: California Exploration Region: Walker-Lane Transition Zone Geothermal Region GEA Development Phase: 2008 USGS Resource Estimate Mean Reservoir Temp: Estimated Reservoir Volume: Mean Capacity: Click "Edit With Form" above to add content History and Infrastructure

289

Surface Indicators of Geothermal Activity at Salt Wells, Nevada...  

Open Energy Info (EERE)

Surface Indicators of Geothermal Activity at Salt Wells, Nevada, USA, Including Warm Ground, Borate Deposits, and Siliceous Alteration Jump to: navigation, search OpenEI Reference...

290

Development Wells At Salt Wells Area (Nevada Bureau of Mines...  

Open Energy Info (EERE)

Development Wells At Salt Wells Area (Nevada Bureau of Mines and Geology, 2009) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Development Wells...

291

Compound and Elemental Analysis At Salt Wells Area (Shevenell...  

Open Energy Info (EERE)

Compound and Elemental Analysis At Salt Wells Area (Shevenell & Garside, 2003) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Compound and...

292

Energy Department Completes Salt Coolant Material Transfer to...  

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

Republic's Ministry of Industry and Trade to complete the transfer of 75 kilograms of fluoride salt from the Department's Oak Ridge National Laboratory (ORNL) to the Czech Nuclear...

293

Electrochemical Behavior of Calcium-Bismuth Alloys in Molten Salt ...  

Science Conference Proceedings (OSTI)

Abstract Scope, The electrochemical properties of calcium-bismuth alloys were investigated to ... Behavior of Silicon Electrodepositing in Fluoride Molten Salts.

294

Natural Convection Fluoride Salt High Temperature Reactor Process ...  

... oil shale processing, hydrogen production, and production of synfuels from coal. The new nuclear reactor design employs a molten salt coolant in a natural ...

295

Regional Gravity Survey of the Northern Great Salt Lake Desert...  

Open Energy Info (EERE)

of the Northern Great Salt Lake Desert and Adjacent Areas in Utah, Nevada, and Idaho Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Regional Gravity...

296

Haynesville-Bossier Shale Play, Texas-Louisiana Salt Basin  

U.S. Energy Information Administration (EIA)

Haynesville-Bossier Shale Play, Texas-Louisiana Salt Basin Source: Energy Information Administration based on data from HPDI, TX Railroad Commission, ...

297

Method for the production of uranium chloride salt  

DOE Patents (OSTI)

A method for the production of UCl.sub.3 salt without the use of hazardous chemicals or multiple apparatuses for synthesis and purification is provided. Uranium metal is combined in a reaction vessel with a metal chloride and a eutectic salt- and heated to a first temperature under vacuum conditions to promote reaction of the uranium metal with the metal chloride for the production of a UCl.sub.3 salt. After the reaction has run substantially to completion, the furnace is heated to a second temperature under vacuum conditions. The second temperature is sufficiently high to selectively vaporize the chloride salts and distill them into a condenser region.

Westphal, Brian R.; Mariani, Robert D.

2013-07-02T23:59:59.000Z

298

Review of the Savannah River Site Salt Waste Processing Facility...  

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

River Site Salt Waste Processing Facility Safety Basis and Design Development May 2011 August 2013 Office of Safety and Emergency Management Evaluations Office of Enforcement...

299

Savannah River Site (SRS) Experience with Preparing Salt Batches  

• Beneficially reuse existing waste. 6 SRS Liquid Waste System Salt Processing. 7 Background • Tk49 is the feed tank to ARP / MCU facilities

300

Molten salt bath circulation design for an electrolytic cell  

DOE Patents (OSTI)

An electrolytic cell for reduction of a metal oxide to a metal and oxygen has an inert anode and an upwardly angled roof covering the inert mode. The angled roof diverts oxygen bubbles into an upcomer channel, thereby agitating a molten salt bath in the upcomer channel and improving dissolution of a metal oxide in the molten salt bath. The molten salt bath has a lower velocity adjacent the inert anode in order to minimize corrosion by substances in the bath. A particularly preferred cell produces aluminum by electrolysis of alumina in a molten salt bath containing aluminum fluoride and sodium fluoride.

Dawless, Robert K. (Monroeville, PA); LaCamera, Alfred F. (Trafford, PA); Troup, R. Lee (Murrysville, PA); Ray, Siba P. (Murrysville, PA); Hosler, Robert B. (Sarver, PA)

1999-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Ion Beam Experiment to Simulate Simultaneous Molten Salt ...  

Science Conference Proceedings (OSTI)

Experiments to expose candidate materials to simultaneous molten salt corrosion and ion-beam damage are staged at the Ion Beam Materials Laboratory at Los ...

302

Molten Salt Electrolysis for the Synthesis of Elemental Boron  

Science Conference Proceedings (OSTI)

An alternative method using molten salt electrolysis was developed in this work. The electrolyte system evaluated was MgF2-NaF-LiF with ...

303

Molten salt bath circulation design for an electrolytic cell  

DOE Patents (OSTI)

An electrolytic cell for reduction of a metal oxide to a metal and oxygen has an inert anode and an upwardly angled roof covering the inert mode. The angled roof diverts oxygen bubbles into an upcomer channel, thereby agitating a molten salt bath in the upcomer channel and improving dissolution of a metal oxide in the molten salt bath. The molten salt bath has a lower velocity adjacent the inert anode in order to minimize corrosion by substances in the bath. A particularly preferred cell produces aluminum by electrolysis of alumina in a molten salt bath containing aluminum fluoride and sodium fluoride. 4 figs.

Dawless, R.K.; LaCamera, A.F.; Troup, R.L.; Ray, S.P.; Hosler, R.B.

1999-08-17T23:59:59.000Z

304

Sensor Technology for Real Time Monitoring of Molten Salt ...  

Science Conference Proceedings (OSTI)

Presentation Title, Sensor Technology for Real Time Monitoring of Molten Salt Electrolytes During Nuclear Fuel Electrorefining. Author(s), Michael F. Simpson, ...

305

Evaluation of the Miamsburg Salt-Gradient, Solar Pond  

SciTech Connect

This project is directed toward data collection and evaluation of the performance of the largest working, salt-gradient, solar pond in the world.

Wittenberg, Layton J.

1978-09-01T23:59:59.000Z

306

In situ parametric study of alkali release in pulverized coal combustion: Effects of operating conditions and gas composition  

Science Conference Proceedings (OSTI)

This work concerns a parametric study of alkali release in a lab-scale, pulverized coal combustor (drop tube reactor) at atmospheric pressure. Measurements were made at steady reactor conditions using excimer laser fragmentation fluorescence (ELIF) and with direct optical access to the flue gas pipe. In this way, absolute gas-phase alkali species could be determined in situ, continuously, with sub-ppb sensitivity, directly in the flue gas. A hard coal was fired in the range 1000-1300{sup o}C, for residence times in the range 3-5 s and for air numbers {lambda} (air/fuel ratios) from 1.15 to 1.50. In addition, the amount of chlorine, water vapor and sulfur, respectively, was increased in known amounts by controlled dosing of HCl, H{sub 2}O and SO{sub 2} into the combustion gas to determine effects of these components on release or capture of the alkali species. The experimental results are also compared with values calculated using ash/fuel analyses and sequential extraction to obtain a fuller picture of alkali release in pulverized fuel combustion. 27 refs., 7 figs., 1 tab.

H. Schuermann; P.B. Monkhouse; S. Unterberger; K.R.G. Hein [Universitaet Stuttgart, Stuttgart (Germany). Institut fuer Verfahrenstechnik und Dampfkesselwesen

2007-07-01T23:59:59.000Z

307

Interactions of hydrogen with alkali promoted Ru/SiO{sub 2} catalysts: A proton NMR study  

DOE Green Energy (OSTI)

Role of H spillover to the silica support was studied using chemisorption; a strongly bound component of spilled over H was found in the silica support which interfered with accurate measurements of active metal sites via volumetric strong H chemisorption. The volumetric chemisorption technique was modified so that measurement times were reduced from 12--36 h to 1 h. The active Ru surface was characterized means of changes in proton spin counts and NMR Knight shifts vs alkali loading. Na, K blocked the active surface of Ru metal, but Cs was pushed off by H chemisorption. The alkali promoters restricted H mobility on both metal surface and at the metal support interfaces; this is consistent with effects on Fischer-Tropsch synthesis. {sup 1}H NMR was used to study the effect of the active metal and promoter on support hydroxyl groups. The OH group density in the silica support decreased with metal and/or promoter loading, but not on a one-to-one basis; the exchange efficiency of the hydroxyls decreased with atomic size of the alkali metal. An additional downfield proton resonance was detected which was assigned to the alkali hydroxide species in the support.

Ozbay, U.D.

1994-05-10T23:59:59.000Z

308

Rheological properties of water-coal slurries based on brown coal in the presence of sodium lignosulfonates and alkali  

Science Conference Proceedings (OSTI)

The effect of the oxidized surface of brown coal on the structural and rheological properties of water-coal slurries was found. The kinetics of structure formation processes in water-coal slurries based on as-received and oxidized brown coal was studied. The effect of lignosulfonate and alkali additives on the samples of brown coal was considered.

D.P. Savitskii; A.S. Makarov; V.A. Zavgorodnii [National Academy of Sciences of Ukraine, Kiev (Ukraine). Dumanskii Institute of Colloid and Water Chemistry

2009-07-01T23:59:59.000Z

309

Ultralow-power local laser control of the dimer density in alkali-metal vapors through photodesorption  

Science Conference Proceedings (OSTI)

Ultralow-power diode-laser radiation is employed to induce photodesorption of cesium from a partially transparent thin-film cesium adsorbate on a solid surface. Using resonant Raman spectroscopy, we demonstrate that this photodesorption process enables an accurate local optical control of the density of dimer molecules in alkali-metal vapors.

Jha, Pankaj K.; Scully, Marlan O. [Texas A and M University, College Station, Texas 77843 (United States); Princeton University, Princeton, New Jersey 08544 (United States); Dorfman, Konstantin E. [Texas A and M University, College Station, Texas 77843 (United States); University of California, Irvine, Irvine, California 92697 (United States); Yi Zhenhuan; Yuan Luqi; Welch, George R. [Texas A and M University, College Station, Texas 77843 (United States); Sautenkov, Vladimir A. [Texas A and M University, College Station, Texas 77843 (United States); Joint Institute of High Temperature, RAS, Moscow 125412 (Russian Federation); Rostovtsev, Yuri V. [University of North Texas, Denton, Texas 76203 (United States); Zheltikov, Aleksei M. [Texas A and M University, College Station, Texas 77843 (United States); M.V. Lomonosov Moscow State University, Moscow 119992 (Russian Federation)

2012-08-27T23:59:59.000Z

310

Savannah River Site - Salt Waste Processing Facility: Briefing on the Salt Waste Processing Facility Independent Technical Review  

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

This is a presentation outlining the Salt Waste Processing Facility process, major risks, approach for conducting reviews, discussion of the findings, and conclusions.

311

Structural restoration of Louann Salt and overlying sediments, De Soto Canyon Salt Basin, northeastern Gulf of Mexico  

E-Print Network (OSTI)

The continental margin of the northeastern Gulf of Mexico is suited for seismic stratigraphic analysis and salt tectonism analysis. Jurassic strata include the Louann Salt on the continental shelf and upper slope of the Destin Dome OCS area, northeastern Gulf of Mexico. These sediments were deposited in a slowly subsiding, stable tectonic environment. Two-dimensional (2-D) seismic data, supplemented with well log, paleontologic and velocity information were used to infer structural and stratigraphic features, especially small faults in the deep part of the De Soto Canyon Salt Basin area. Six sequence boundaries or correlative paleohorizons were interpreted on Landmark seismic interpretation workstation. They are Base of Salt or Equivalent, Top of Salt, Top of Smackover Formation, Top of Cotton Valley Group, Middle Cretaceous sequence boundary, and Top of Upper Cretaceous. Information generated from structural and stratigraphic analysis are used to analyze the evolution of salt movement and salt mechanism in this area. I used a software package Restore (Dan Schultz-Ela and Ken Duncan, 1991) for structural restoration. This program is suitable for extensional terrane. The restoration of one depth section was achieved through steps introduced by Restore. Regional extension, gravity spreading, and gliding are the most important mechanism of salt flow, buoyancy and differential loading mainly contribute to the vertical development of salt structure in this area.

Guo, Mengdong

1997-01-01T23:59:59.000Z

312

Alkali removal at about 1400{sup o}C for the pressurized pulverized coal combustion combined cycle. 1. Thermodynamics and concept  

SciTech Connect

The limitation of fossil fuel resources and the necessity of reducing CO{sub 2} emission require an increase of the efficiency of power plants by using combined cycle power systems. The pressurized pulverized coal combustion (PPCC) combined cycle is a coal fired combined cycle concept which is able to achieve efficiencies in excess of 53%. The direct use of the hot flue gas for driving a gas turbine requires a hot gas cleanup to achieve corrosion prevention of the turbine blading. One of the main problems is the release of alkalis during the coal combustion process. Therefore, the thermodynamic basics for the control of alkali vapor pressures in the hot flue gas of PPCC have been investigated by thermodynamic equilibrium calculations and Knudsen effusion mass spectrometric measurements on alkali oxide activities in and alkali partial pressures over coal ash slags with and without additives and alkali laden model sorbents. The obtained results reveal that the requirements of the gas turbine manufacturers regarding alkali concentration in the hot flue gas should be satisfiable by certain aluminosilicate sorbents. On the basis of these results, a concept for alkali vapor removal is proposed. 20 refs., 9 figs., 2 tabs.

Winfried Willenborg; Michael Mueller; Klaus Hilpert [Forschungszentrum Juelich GmbH, Juelich (Germany)

2006-12-15T23:59:59.000Z

313

Ketone Production from the Thermal Decomposition of Carboxylate Salts  

E-Print Network (OSTI)

The MixAlco process uses an anaerobic, mixed-culture fermentation to convert lignocellulosic biomass to carboxylate salts. The fermentation broth must be clarified so that only carboxylate salts, water, and minimal impurities remain. Carboxylate salts are concentrated by evaporation and thermally decomposed into ketones. The ketones can then be chemically converted to a wide variety of chemicals and fuels. The presence of excess lime in the thermal decomposition step reduced product yield. Mixtures of calcium carboxylate salts were thermally decomposed at 450 degrees C. Low lime-to-salt ratios (g Ca(OH)2/g salt) of 0.00134 and less had a negligible effect on ketone yield. In contrast, salts with higher lime-to-salt ratios of 0.00461, 0.0190, and 0.272 showed 3.5, 4.6, and 9.4% loss in ketone yield, respectively. These losses were caused primarily by increases in tars and heavy oils; however, a three-fold increase in hydrocarbon production occurred as well. To predict ketone product distribution, a random-pairing and a Gibbs free energy minimization model were applied to thermal decompositions of mixed calcium and sodium carboxylate salts. Random pairing appears to better predict ketone product composition. For sodium and calcium acetate, two types of mixed sodium carboxylate salts, and two types of mixed calcium carboxylate salts, activation energy (EA) was determined using three isoconversional methods. For each salt type, EA varied significantly with conversion. The average EA for sodium and calcium acetate was 226.65 and 556.75 kJ/mol, respectively. The average EA for the two mixed sodium carboxylate salts were 195.61, and 218.18 kJ/mol. The average EA for the two mixed calcium carboxylate salts were 232.78, and 176.55 kJ/mol. In addition, three functions of conversion were employed to see which one best modeled the experimental data. The Sestak-Berggren model was the best overall. Possible reactor designs and configurations that address the challenges associated with the continuous thermal decomposition of carboxylate salts are also presented and discussed. Methods of fermentation broth clarification were tested. Flocculation showed little improvement in broth purity. Coagulation yielded broth of 93.23% purity. Filtration using pore sizes from 1 micrometer to 240 Daltons increased broth purity (90.79 to 98.33%) with decreasing pore size.

Landoll, Michael 1984-

2012-12-01T23:59:59.000Z

314

Development of laser optogalvanic spectroscopy as a probe of alkali atoms in an MHD environment  

DOE Green Energy (OSTI)

Application of Laser Optogalvanic Spectroscopy (LOGS) to MHD combustion systems requires selection of an appropriate alkali atom electronic transition to monitor. These studies suggest that in MHD combustion systems, it is desirable to use cesium, which occurs as an impurity in potassium compounds, as a surrogate for potassium rather than to directly monitor potassium in order to obtain reliable determinations of seed concentration. Studies were also performed to investigate the effect of electrode corrosion on the normalized LOGS signal intensity at a fixed wavelength (578.238 nm). During six-hour experiments in a near-stoichiometric flame, the normalized LOGS signal intensity decreased by 40-50% for a -960 V rod electrode and by 10-20% for a -500 V rod electrode. These changes are attributed to buildup of an oxide coating on the electrode, reducing the collection efficiency of the electrode.

Monts, D.L.; Qian, S.; Cook, R.L.; Shepard, W.S.

1995-02-01T23:59:59.000Z

315

Sputtering and secondary ion emission properties of alkali metal films and adsorbed monolayers  

Science Conference Proceedings (OSTI)

The secondary ion emission of alkali metal adsorbed monlayer and multilayer films has been studied. Profiling with sub-monolayer resolution has been performed by Auger, x-ray photoemission and secondary ion mass spectroscopy. Characteristic differences in the sputtering yields, and ion fraction have been observed which are associated with both the surface bonding properties and the mechanism leading to the formation of secondary ions. By sputtering with a negative bias applied to the sample, positive secondary ions are returned to the surface, resulting in a reduced sputter-induced erosion rate. Comparison with the results obtained with K and Li overlayers sputtered without sample bias provides an experimental value of both the total and secondary ion sputtering yields. The first and second monolayers can be readily identified and the first monolayer exhibits a lower sputtering yield and higher secondary ion fraction. This result is related to adsorption theory and measured values are compared with those obtained by thermal desorption measurements.

Krauss, A R; Gruen, D M

1980-01-01T23:59:59.000Z

316

Energy conservation in the primary aluminum and chlor-alkali industries  

SciTech Connect

The primary aluminum and chlor-alkali industries together use nearly 13% of the electrical energy consumed by US industry. As part of its mission to promote energy conservation in basic US industries, the DOE surveys the present technological status of the major electrochemical industries and evaluates promising technological innovations that may lead to reduced energy requirements. This study provides technical and economic analyses in support of a government program of research and development in advanced electrolytic technology. This program is intended to supplement the development efforts directed toward energy savings by private industry. Sections II and III of this report cover aluminum and chlorine production processes only, since these two industries represent over 90% of the electrical energy requirements of all electrolytic industries in the United States. Section IV examines barriers to accelerated research and development by the electrolytic industries, and makes suggestions for government actions to overcome these barriers.

1980-10-01T23:59:59.000Z

317

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

318

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

319

Molten Salt Nanomaterials for Thermal Energy Storage and Concentrated Solar Power Applications  

E-Print Network (OSTI)

The thermal efficiency of concentrated solar power (CSP) system depends on the maximum operating temperature of the system which is determined by the operating temperature of the TES device. Organic materials (such as synthetic oil, fatty acid, or paraffin wax) are typically used for TES. This limits the operating temperature of CSP units to below 400 degrees C. Increasing the operating temperature to 560 degrees C (i.e., the creeping temperature of stainless steel), can enhance the theoretical thermal efficiency from 54 percent to 63 percent. However, very few thermal storage materials are compatible for these high temperatures. Molten salts are thermally stable up to 600 degrees C and beyond. Using the molten salts as the TES materials confers several benefits, which include: (1) Higher operating temperature can significantly increase the overall cycle efficiency and resulting costs of power production. (2) Low cost of the molten salt materials can drastically reduce the cost. (3) The molten salts, which are environmentally safe, can also reduce the potential environmental impact. However, these materials suffer from poor thermo-physical properties. Impregnating these materials with nanoparticles can enhance these properties. Solvents doped with nanoparticles are termed as nanofluids. Nanofluids have been reported in the literature for the anomalous enhancement of their thermo-physical properties. In this study, the poor thermal properties of the molten salts were enhanced dramatically on mixing with nanoparticles. For example the specific heat capacity of these molten salt eutectics was found to be enhanced by as much as ~ 26 percent on mixing with nanoparticles at a mass fraction of ~ 1 percent. The resultant properties of these nanomaterials were found to be highly sensitive to small variations in the synthesis protocols. Computational models were also developed in this study to explore the fundamental transport mechanisms on the molecular scale for elucidating the anomalous enhancements in the thermo-physical properties that were measured in these experiments. This study is applicable for thermal energy storage systems utilized for other energy conversion technologies – such as geothermal energy, nuclear energy and a combination of energy generation technologies.

Shin, Donghyun

2011-08-01T23:59:59.000Z

320

Disposal of NORM waste in salt caverns  

Science Conference Proceedings (OSTI)

Some types of oil and gas production and processing wastes contain naturally occurring radioactive materials (NORM). If NORM is present at concentrations above regulatory levels in oil field waste, the waste requires special disposal practices. The existing disposal options for wastes containing NORM are limited and costly. This paper evaluates the legality, technical feasibility, economics, and human health risk of disposing of NORM-contaminated oil field wastes in salt caverns. Cavern disposal of NORM waste is technically feasible and poses a very low human health risk. From a legal perspective, there are no fatal flaws that would prevent a state regulatory agency from approving cavern disposal of NORM. On the basis of the costs charged by caverns currently used for disposal of nonhazardous oil field waste (NOW), NORM waste disposal caverns could be cost competitive with existing NORM waste disposal methods when regulatory agencies approve the practice.

Veil, J.A.; Smith, K.P.; Tomasko, D.; Elcock, D.; Blunt, D.; Williams, G.P.

1998-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Technical review of Molten Salt Oxidation  

Science Conference Proceedings (OSTI)

The process was reviewed for destruction of mixed low-level radioactive waste. Results: extensive development work and scaleup has been documented on coal gasification and hazardous waste which forms a strong experience base for this MSO process; it is clearly applicable to DOE wastes such as organic liquids and low-ash wastes. It also has potential for processing difficult-to-treat wastes such as nuclear grade graphite and TBP, and it may be suitable for other problem waste streams such as sodium metal. MSO operating systems may be constructed in relatively small units for small quantity generators. Public perceptions could be favorable if acceptable performance data are presented fairly; MSO will likely require compliance with regulations for incineration. Use of MSO for offgas treatment may be complicated by salt carryover. Figs, tabs, refs.

Not Available

1993-12-01T23:59:59.000Z

322

Visualization of salt-induced stress perturbations.  

Science Conference Proceedings (OSTI)

An important challenge encountered during post-processing of finite element analyses is the visualizing of three-dimensional fields of real-valued second-order tensors. Namely, as finite element meshes become more complex and detailed, evaluation and presentation of the principal stresses becomes correspondingly problematic. In this paper, we describe techniques used to visualize simulations of perturbed in-situ stress fields associated with hypothetical salt bodies in the Gulf of Mexico. We present an adaptation of the Mohr diagram, a graphical paper and pencil method used by the material mechanics community for estimating coordinate transformations for stress tensors, as a new tensor glyph for dynamically exploring tensor variables within three-dimensional finite element models. This interactive glyph can be used as either a probe or a filter through brushing and linking.

Crossno, Patricia Joyce; Brannon, Rebecca Moss; Coblentz, David D.; Rogers, David H.

2004-10-01T23:59:59.000Z

323

Salt River Project SRP | Open Energy Information  

Open Energy Info (EERE)

SRP SRP Jump to: navigation, search Name Salt River Project (SRP) Place Tempe, Arizona Zip 85281-1298 Sector Biomass, Solar Product US utility which sources a percentage of its electricity from biomass plants. It is also involved in the solar power industry. Coordinates 33.42551°, -111.937419° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":33.42551,"lon":-111.937419,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

324

May 29, 2010 The Hard Sell on Salt  

E-Print Network (OSTI)

May 29, 2010 The Hard Sell on Salt By MICHAEL MOSS With salt under attack for its ill effects -- an allure the industry has recognized for decades. "Once a preference is acquired," a top scientist at Frito adopting the lower standard for everyone as part of its review of nutrition standards. The food industry

Bent, Andrew F.

325

Treatment of plutonium process residues by molten salt oxidation  

Science Conference Proceedings (OSTI)

Molten Salt Oxidation (MSO) is a thermal process that can remove more than 99.999% of the organic matrix from combustible {sup 238}Pu material. Plutonium processing residues are injected into a molten salt bed with an excess of air. The salt (sodium carbonate) functions as a catalyst for the conversion of the organic material to carbon dioxide and water. Reactive species such as fluorine, chlorine, bromine, iodine, sulfur, phosphorous and arsenic in the organic waste react with the molten salt to form the corresponding neutralized salts, NaF, NaCl, NaBr, NaI, Na{sub 2}SO{sub 4}, Na{sub 3}PO{sub 4} and NaAsO{sub 2} or Na{sub 3}AsO4. Plutonium and other metals react with the molten salt and air to form metal salts or oxides. Saturated salt will be recycled and aqueous chemical separation will be used to recover the {sup 238}Pu. The Los Alamos National Laboratory system, which is currently in the conceptual design stage, will be scaled down from current systems for use inside a glovebox.

Stimmel, J.; Wishau, R.; Ramsey, K.B.; Montoya, A.; Brock, J. [Los Alamos National Lab., NM (United States); Heslop, M. [Naval Surface Warfare Center (United States). Indian Head Div.; Wernly, K. [Molten Salt Oxidation Corp. (United States)

1999-04-01T23:59:59.000Z

326

Controlled Source Frequency-Domain Magnetics At Salt Wells Area  

Open Energy Info (EERE)

Controlled Source Frequency-Domain Magnetics At Salt Wells Area Controlled Source Frequency-Domain Magnetics At Salt Wells Area (Montgomery, Et Al., 2005) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Controlled Source Frequency-Domain Magnetics At Salt Wells Area (Montgomery, Et Al., 2005) Exploration Activity Details Location Salt Wells Area Exploration Technique Controlled Source Frequency-Domain Magnetics Activity Date 2004 - 2004 Usefulness useful DOE-funding Unknown Exploration Basis AMP Resource contracted Willowstick Technologies, LLC to conduct a Controlled Source-Frequency Domain Magnetics (CS-FDM) geophysical investigation at Salt Wells in order to characterize and delineate areas showing the greatest concentrations and highest temperatures of geothermal groundwater. The investigation also sought to map blind faults beneath the

327

Independent Oversight Review, Savannah River Site Salt Waste Processing  

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

Savannah River Site Salt Waste Savannah River Site Salt Waste Processing Facility - August 2013 Independent Oversight Review, Savannah River Site Salt Waste Processing Facility - August 2013 August 2013 Review of the Savannah River Site Salt Waste Processing Facility Safety Basis and Design Development. This report documents the results of an independent oversight review of the safety basis and design development for the Salt Waste Processing Facility (SWPF) at the U.S. Department of Energy (DOE) Savannah River Site. The review was performed February 12-14, 2013 by DOE's Office of Safety and Emergency Management Evaluations, which is within the DOE Office of Health, Safety and Security. The purpose of the review was to evaluate the safety basis, design, and the associated technical documents developed for

328

BLM Fact Sheet- Ormat Technologies Salt Wells Geothermal Energy Project |  

Open Energy Info (EERE)

BLM Fact Sheet- Ormat Technologies Salt Wells Geothermal Energy Project BLM Fact Sheet- Ormat Technologies Salt Wells Geothermal Energy Project Jump to: navigation, search OpenEI Reference LibraryAdd to library Report: BLM Fact Sheet- Ormat Technologies Salt Wells Geothermal Energy Project Abstract No abstract available. Author Bureau of Land Management Organization Bureau of Land Management, Carson City Field Office, Nevada Published U.S. Department of the Interior, 2011 DOI Not Provided Check for DOI availability: http://crossref.org Online Internet link for BLM Fact Sheet- Ormat Technologies Salt Wells Geothermal Energy Project Citation Bureau of Land Management (Bureau of Land Management, Carson City Field Office, Nevada). 2011. BLM Fact Sheet- Ormat Technologies Salt Wells Geothermal Energy Project. Carson City, Nevada: U.S. Department of the

329

Independent Oversight Review, Savannah River Site Salt Waste Processing  

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

Savannah River Site Salt Waste Savannah River Site Salt Waste Processing Facility - August 2013 Independent Oversight Review, Savannah River Site Salt Waste Processing Facility - August 2013 August 2013 Review of the Savannah River Site Salt Waste Processing Facility Safety Basis and Design Development. This report documents the results of an independent oversight review of the safety basis and design development for the Salt Waste Processing Facility (SWPF) at the U.S. Department of Energy (DOE) Savannah River Site. The review was performed February 12-14, 2013 by DOE's Office of Safety and Emergency Management Evaluations, which is within the DOE Office of Health, Safety and Security. The purpose of the review was to evaluate the safety basis, design, and the associated technical documents developed for

330

ENEL Salt Wells Geothermal Facility | Open Energy Information  

Open Energy Info (EERE)

ENEL Salt Wells Geothermal Facility ENEL Salt Wells Geothermal Facility Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home ENEL Salt Wells Geothermal Facility General Information Name ENEL Salt Wells Geothermal Facility Facility Salt Wells Geothermal Facility Sector Geothermal energy Location Information Location Churchill, NV Coordinates 39.651603422063°, -118.49778413773° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":39.651603422063,"lon":-118.49778413773,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

331

Method for Making a Uranium Chloride Salt Product  

DOE Patents (OSTI)

The subject apparatus provides a means to produce UCl3, in large quantities without incurring corrosion of the containment vessel or associated apparatus. Gaseous Cl is injected into a lower layer of Cd where CdCl2 is formed. Due to is lower density, the CdCl2 rises through the Cd layer into a layer of molten LiCl-KCL salt where a rotatable basket containing uranium ingots is suspended. The CdCl2 reacts with the uranium to form UCl, and Cd. Due to density differences, the Cd sinks down to the liquid Cd layer and is reused. The UCl3 combines with the molten salt. During production the temperature is maintained at about 600 degrees C. while after the uranium has been depleted the salt temperature is lowered, the molten salt is pressure siphoned from the vessel, and the salt product LiCl-KCl-30 mol% UCl3 is solidified.

Miller, William F.; Tomczuk, Zygmunt

2004-10-05T23:59:59.000Z

332

Continuous extraction of molten chloride salts with liquid cadmium alloys  

Science Conference Proceedings (OSTI)

A pyrochemical method is being developed at Argonne National Laboratory (ANL) to provide contnuous multistage extractions between molten chloride salts and liquid cadmium alloys at 500{degrees}C. The extraction method will be used to recover transuranic (TRU) elements from the process salt in the electroretiner used in the pyrochemical reprocessing of spent fuel from the Integral Fast Reactor (IFR). The IFR is one of the Department of Energy`s advanced power reactor concepts. The recovered TRU elements are returned to the electrorefiner. The extracted salt undergoes further processing to remove rare earths and other fission products so that most of the purified salt can also be returned to the electrorefiner, thereby extending the useful life of the process salt many times.

Chow, L.S.; Basco, J.K.; Ackerman, J.P.; Johnson, T.R.

1993-09-01T23:59:59.000Z

333

Factors influencing algal biomass in hydrologically dynamic salt ponds in a subtropical salt marsh  

E-Print Network (OSTI)

The interface between land and water is often a dynamic zone that responds to relatively short-term climatic and hydrologic forces. Coastal salt marshes occupy this zone between land and sea and typically are comprised of vegetated marsh intersected by channels and shallow ponds that are subject to flooding by winds, tides, and storm surges. Coastal salt marshes are widely regarded as zones of high macrophyte productivity. However, microalgae may contribute more to salt marsh productivity than previously realized, underscoring the importance of understanding algal dynamics in such systems. Benthic and planktonic chlorophyll-a (surrogate for total algal biomass), sediment AFDW, total suspended solids, salinity, and nutrients were examined in marsh ponds in the subtropical Guadalupe Estuary, TX, USA to determine the effects of hydrologic connections on algal biomass in this system. From May 2005 – May 2006 there were several pond connection, disconnection, and desiccation events. During periods of disconnection, algal biomass was higher in both the benthos and the water column than during connection events when supposed flushing occurred. Connection events also flushed out high NH4 accumulating in pond surface waters, but did not increase NOx. Therefore, the primary source of DIN seemed to be nutrient cycling within the ponds. There was a temporal effect on surface water salinity, which increased throughout the sampling period as bay water levels and subsequent pond connections decreased, demonstrating interannual variability and the link between seasons (wet vs. dry) and marsh inundation patterns (high water periods vs. low water periods) in this estuary.

Miller, Carrie J.

2007-05-01T23:59:59.000Z

334

Analysis of Multistage and Other Creep Data for Domal Salts  

SciTech Connect

There have existed for some time relatively sparse creep databases for a number of domal salts. Although all of these data were analyzed at the time they were reported, to date there has not been a comprehensive, overall evaluation within the same analysis framework. Such an evaluation may prove of value. The analysis methodology is based on the Multimechanism Deformation (M-D) description of salt creep and the corresponding model parameters determined from conventional creep tests. The constitutive model of creep wss formulated through application of principles involved in micromechanical modeling. It was possible, at minimum, to obtain the steady state parameters of the creep model from the data on the domal salts. When this was done, the creep of the domal salts, as compared to the well-defined Waste Isolation Pilot Plant (WIPP) bedded clean salt, was either essentially identical to, or significantly harder (more creep resistant) than WIPP salt. Interestingly, the domal salts form two distinct groups, either sofl or hard, where the difference is roughly a factor often in creep rate between the twcl groups. As might be expected, this classification corresponds quite well to the differences in magnitude of effective creep volume losses of the Strategic Petroleum Reserve (SPR) caverns as determined by the CAVEMAN cavern pressure history analysis, depending upon the specific dome or region within the dome. Creep response shoulcl also correlate to interior cavern conditions that produce salt falls. WMle, in general, the caverns in hard sah have a noticeably greater propensity for salt falls, a smaller number of similar events are exhibited even in the caverns in soft salt.

Munson, D.E.

1998-10-01T23:59:59.000Z

335

A fixed granular-bed sorber for measurement and control of alkali vapors in PFBC (pressurized fluidized-bed combustion)  

SciTech Connect

Alkali vapors (Na and K) in the hot flue gas from the pressurized fluidized-bed combustion (PFBC) of coal could cause corrosion problems with the gas turbine blades. In a laboratory-scale PFBC test with Beulah lignite, a fixed granular bed of activated bauxite sorbent was used to demonstrate its capability for measuring and controlling alkali vapors in the PFBC flue gas. The Beulah lignite was combusted in a bed of Tymochtee dolomite at bed temperatures ranging from 850 to 875{degrees}C and a system pressure of 9.2 atm absolute. The time-averaged concentration of sodium vapor in the PFBC flue gas was determined from the analysis of two identical beds of activated bauxite and found to be 1.42 and 1.50 ppmW. The potassium vapor concentration was determined to be 0.10 ppmW. The sodium material balance showed that only 0.24% of the total sodium in the lignite was released as vapor species in the PFBC flue gas. This results in an average of 1.56 ppmW alkali vapors in the PFBC flue gas. This average is more than 1.5 orders of magnitude greater than the currently suggested alkali specification limit of 0.024 ppm for an industrial gas turbine. The adsorption data obtained with the activated bauxite beds were also analyzed mathematically by use of a LUB (length of unused bed)/equilibrium section concept. Analytical results showed that the length of the bed, L{sub o} in centimeters, relates to the break through time, {theta}{sub b} in hours, for the alkali vapor to break through the bed as follows: L{sub o} = 33.02 + 1.99 {theta}{sub b}. This formula provides useful information for the engineering design of fixed-bed activated bauxite sorbers for the measurement and control of alkali vapors in PFBC flue gas. 26 refs., 4 figs., 4 tabs.

Lee, S.H.D.; Swift, W.M.

1990-01-01T23:59:59.000Z

336

In-Drift Precipitates/Salts Analysis  

SciTech Connect

As directed by a written development plan (CRWMS M&O 1999a), an analysis of the effects of salts and precipitates on the repository chemical environment is to be developed and documented in an Analyses/Model Report (AMR). The purpose of this analysis is to assist Performance Assessment Operations (PAO) and the Engineered Barrier Performance Department in modeling the geochemical environment within a repository drift, thus allowing PAO to provide a more detailed and complete in-drift geochemical model abstraction and to answer the key technical issues (KTI) raised in the NRC Issue Resolution Status Report (IRSR) for the Evolution of the Near Field Environment (NFE) Revision 2 (NRC 1999). The purpose of this ICN is to qualify and document qualification of the AMR's technical products. The scope of this document is to develop a model of the processes that govern salt precipitation and dissolution and resulting water composition in the Engineered Barrier System (EBS). This model is developed to serve as a basis for the in-drift geochemical modeling work performed by PAO and is to be used in subsequent PAO analyses including the EBS physical and chemical model abstraction effort. However, the concepts may also apply to some near and far field geochemical processes and can have conceptual application within the unsaturated zone and saturated zone transport modeling efforts. The intended use of the model developed in this report is to estimate, within an appropriate level of confidence, the pH, chloride concentration, and ionic strength of water on the drip shield or other location within the drift during the post-closure period. These estimates are based on evaporative processes that are subject to a broad range of potential environmental conditions and are independent of the presence or absence of backfill. An additional intended use is to estimate the environmental conditions required for complete vaporization of water. The presence and composition of liquid water in the drift (i.e., pH, chloride concentration, and ionic strength) are potentially important to corrosion and radionuclide transport calculations performed by PAO.

P. Mariner

2001-01-10T23:59:59.000Z

337

The Effects of Using Alkali-Silica Reaction Affected Recycled Concrete Aggregate in Hot Mix Asphalt  

E-Print Network (OSTI)

The effects of using alkali-silica reaction (ASR) affected recycled concrete aggregate (ASR-RCA) in hot mix asphalt (HMA) were investigated in this study. Dilatometer and modified beam tests were performed to determine the possibility of new ASR occurring in reactive aggregates within the HMA or re-expansion of existing gel. The Lottman test and micro-calorimeter were used to determine the moisture susceptibility of HMA made with ASR-RCA. A differential scanning calorimeter (DSC) with thermogravimetric analysis (TGA) was used to evaluate the drying of an artificial gel and x-ray diffraction (XRD) was used to check for the potential presence of gel in the filler fraction of the ASR-RCAs. Micro-deval and freeze-thaw tests were evaluated for their potential to indicate the presence of excess micro-cracks or ASR gel. Expansion testing indicated that both ASR-RCAs were still reactive with 0.5 N NaOH solution saturated with calcium hydroxide (CH) at 60 degrees C. Dilatometer testing of HMA specimens in NaOH CH solution at 60 degrees C indicated a reaction between the asphalt binder and the solution, but little, if any, ASR. The lack of expansion in the modified beam test supports the binder-solution interaction. However, dilatometer testing in deicer solution at the same temperature indicated that some ASR may have occurred along with the primary binder-solution interaction. The volume change characteristics associated with the binder-solution interaction with and without ASR was supported by the change in pH and alkali concentration of the test solution. DSC/TGA testing indicated that the artificial gel dehydrated at approximately 100 degrees C. XRD analysis of the filler indicated that some gel may have accumulated in this fraction. Moisture damage testing indicated good resistance to moisture damage by HMA mixtures made with ASR-RCA especially compared to a virgin siliceous aggregate. Micro-deval and freeze-thaw tests can detect the presence of micro-cracks due to ASR in ASR-RCAs as higher mass loss than the virgin aggregate. The potential distress mechanisms that may occur when using ASR-RCA in an HMA pavement were identified. Results obtained using accelerated laboratory conditions were extrapolated based on anticipated field conditions. Guidelines for the mitigation of potential distresses in HMA made with ASR-RCA are presented.

Geiger, Brian James

2010-08-01T23:59:59.000Z

338

Gradient zone boundary control in salt gradient solar ponds  

SciTech Connect

A method and apparatus for suppressing zone boundary migration in a salt gradient solar pond includes extending perforated membranes across the pond at the boundaries, between the convective and non-convective zones, the perforations being small enough in size to prevent individual turbulence disturbances from penetrating the hole, but being large enough to allow easy molecular diffusion of salt thereby preventing the formation of convective zones in the gradient layer. The total area of the perforations is a sizable fraction of the membrane area to allow sufficient salt diffusion while preventing turbulent entrainment into the gradient zone.

Hull, John R. (Downers Grove, IL)

1984-01-01T23:59:59.000Z

339

Molten salt/metal extractions for recovery of transuranic elements  

SciTech Connect

The integral fast reactor (EFR) is an advanced reactor concept that incorporates metallic driver and blanket fuels, an inherently safe, liquid-sodium-cooled, pool-type, reactor design, and on-site pyrochemical reprocessing (including electrorefining) of spent fuels and wastes. This paper describes a pyrochemical method that is being developed at Argonne National Laboratory to recover transuranic elements from the EFR electrorefiner process salt. The method uses multistage extractions between molten chloride salts and cadmium metal at high temperatures. The chemical basis of the salt extraction method, the test equipment, and a test plan are discussed.

Chow, L.S.; Basco, J.K.; Ackerman, J.P.; Johnson, T.R.

1992-01-01T23:59:59.000Z

340

Molten salt/metal extractions for recovery of transuranic elements  

SciTech Connect

The integral fast reactor (EFR) is an advanced reactor concept that incorporates metallic driver and blanket fuels, an inherently safe, liquid-sodium-cooled, pool-type, reactor design, and on-site pyrochemical reprocessing (including electrorefining) of spent fuels and wastes. This paper describes a pyrochemical method that is being developed at Argonne National Laboratory to recover transuranic elements from the EFR electrorefiner process salt. The method uses multistage extractions between molten chloride salts and cadmium metal at high temperatures. The chemical basis of the salt extraction method, the test equipment, and a test plan are discussed.

Chow, L.S.; Basco, J.K.; Ackerman, J.P.; Johnson, T.R.

1992-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

The Thorium Molten Salt Reactor Moving on from the MSBR  

E-Print Network (OSTI)

A re-evaluation of the Molten Salt Breeder Reactor concept has revealed problems related to its safety and to the complexity of the reprocessing considered. A reflection is carried out anew in view of finding innovative solutions leading to the Thorium Molten Salt Reactor concept. Several main constraints are established and serve as guides to parametric evaluations. These then give an understanding of the influence of important core parameters on the reactor's operation. The aim of this paper is to discuss this vast research domain and to single out the Molten Salt Reactor configurations that deserve further evaluation.

Mathieu, L; Brissot, R; Le Brun, C; Liatard, E; Loiseaux, J M; Méplan, O; Merle-Lucotte, E; Nuttin, A; Wilson, J; Garzenne, C; Lecarpentier, D; Walle, E

2006-01-01T23:59:59.000Z

342

The Thorium Molten Salt Reactor : Moving on from the MSBR  

E-Print Network (OSTI)

A re-evaluation of the Molten Salt Breeder Reactor concept has revealed problems related to its safety and to the complexity of the reprocessing considered. A reflection is carried out anew in view of finding innovative solutions leading to the Thorium Molten Salt Reactor concept. Several main constraints are established and serve as guides to parametric evaluations. These then give an understanding of the influence of important core parameters on the reactor's operation. The aim of this paper is to discuss this vast research domain and to single out the Molten Salt Reactor configurations that deserve further evaluation.

L. Mathieu; D. Heuer; R. Brissot; C. Le Brun; E. Liatard; J. M. Loiseaux; O. Méplan; E. Merle-Lucotte; A. Nuttin; J. Wilson; C. Garzenne; D. Lecarpentier; E. Walle; the GEDEPEON Collaboration

2005-06-02T23:59:59.000Z

343

Engineering Evaluation of Proposed Alternative Salt Transfer Method for the Molten Salt Reactor Experiement for the Oak Ridge National Laboratory  

SciTech Connect

This evaluation was performed by Pro2Serve in accordance with the Technical Specification for an Engineering Evaluation of the Proposed Alternative Salt Transfer Method for the Molten Salt Reactor Experiment at the Oak Ridge National Laboratory (BJC 2009b). The evaluators reviewed the Engineering Evaluation Work Plan for Molten Salt Reactor Experiment Residual Salt Removal, Oak Ridge National Laboratory, Oak Ridge, Tennessee (DOE 2008). The Work Plan (DOE 2008) involves installing a salt transfer probe and new drain line into the Fuel Drain Tanks and Fuel Flush Tank and connecting them to the new salt transfer line at the drain tank cell shield. The probe is to be inserted through the tank ball valve and the molten salt to the bottom of the tank. The tank would then be pressurized through the Reactive Gas Removal System to force the salt into the salt canisters. The Evaluation Team reviewed the work plan, interviewed site personnel, reviewed numerous documents on the Molten Salt Reactor (Sects. 7 and 8), and inspected the probes planned to be used for the transfer. Based on several concerns identified during this review, the team recommends not proceeding with the salt transfer via the proposed alternate salt transfer method. The major concerns identified during this evaluation are: (1) Structural integrity of the tanks - The main concern is with the corrosion that occurred during the fluorination phase of the uranium removal process. This may also apply to the salt transfer line for the Fuel Flush Tank. Corrosion Associated with Fluorination in the Oak Ridge National Laboratory Fluoride Volatility Process (Litman 1961) shows that this problem is significant. (2) Continued generation of Fluorine - Although the generation of Fluorine will be at a lower rate than experienced before the uranium removal, it will continue to be generated. This needs to be taken into consideration regardless of what actions are taken with the salt. (3) More than one phase of material - There are likely multiple phases of material in the salt (metal or compound), either suspended through the salt matrix, layered in the bottom of the tank, or both. These phases may contribute to plugging during any planned transfer. There is not enough data to know for sure. (4) Probe heat trace - The alternate transfer method does not include heat tracing of the bottom of the probe. There is a concern that this may cool the salt and other phases of materials present enough to block the flow of salt. (5) Stress-corrosion cracking - Additionally, there is a concern regarding moisture that may have been introduced into the tanks. Due to time constraints, this concern was not validated. However, if moisture was introduced into the tanks and not removed during heating the tanks before HF and F2 sparging, there would be an additional concern regarding the potential for stress-corrosion cracking of the tank walls.

Carlberg, Jon A.; Roberts, Kenneth T.; Kollie, Thomas G.; Little, Leslie E.; Brady, Sherman D.

2009-09-30T23:59:59.000Z

344

Estimation Of Retained Crude Oil Associated With Crushed Salt And Salt Cores In The Presence Of Near-Saturated Brine  

E-Print Network (OSTI)

This paper describes three experiments whose purpose is to determine the amount of retained oil on massive salt surfaces and in crushed salt in the presence of water and brine. These experiments have application to the decommissioning process for the Weeks Island mine. In the first experiment, oil-coated salt cores were immersed in either fresh water or in 85% brine. In the case of both fluids, the oil was completely removed from the cores within several hours. In the second experiment, oil-coated salt pieces were suspended in air and the oil was allowed to drain. The weight of retained oil clinging to the salt was determined. This experiment was used to estimate the total amount of oil clinging to the roofs of the mine. The total amount of oil clinging to the roofs of the mine is estimated to be between 240 and 400 m 3 (1500 and 2500 BBL). In the third experiment, a pan of oil-soaked crushed salt was immersed in 85% brine, and oil removal from the salt was monitored as a function of...

Timothy Hern Energetic; Timothy J. O’hern; Thomas E. Hinkebein; Thomas W. Grasser

1999-01-01T23:59:59.000Z

345

The influence of high quantity of fly ash on reducing the expansion due to ASR in the presence of alkalis  

E-Print Network (OSTI)

A testing program was devised to study the role of high volume fly ash (HVFA) in reducing the expansion caused by alkali-silica reaction (ASR). A series of modified ASTM C 1260 tests were performed, where the replacement of cement by Class F fly ash was 58% by mass of cement. A reactive siliceous aggregate was used. The influence of inherent alkalis in cement to the reaction was also studied. The test results confirm that HVFA significantly helps in controlling expansion caused by ASR. The test period was extended to 28 days to assess if more reproducible results can be obtained. The results indicate that reducing the alkalinity of the sodium hydroxide solution by 50%, to 0.5N is sufficient to determine the potential reactivity of aggregates. The reduction of alkalinity of sodium hydroxide to 0.25N, however, produced results, which were beyond interpretation. Concrete using High Volume Fly Ash was tested for strength to ascertain if the reactive aggregates or the percentage of internal alkalis in the cement influenced the strength. This report discusses the test results for only part of a broader research program in progress at the Texas Transportation Institute, Texas A&M University.

Mohidekar, Saleel D.

2000-01-01T23:59:59.000Z

346

Ethanol production with dilute acid hydrolysis using partially dried lignocellulosics  

DOE Patents (OSTI)

A process of converting lignocellulosic biomass to ethanol, comprising hydrolyzing lignocellulosic materials by subjecting dried lignocellulosic material in a reactor to a catalyst comprised of a dilute solution of a strong acid and a metal salt to lower the activation energy (i.e., the temperature) of cellulose hydrolysis and ultimately obtain higher sugar yields.

Nguyen, Quang A. (Chesterfield, MO); Keller, Fred A. (Lakewood, CO); Tucker, Melvin P. (Lakewood, CO)

2003-12-09T23:59:59.000Z

347

The Influence of Lewis Acid/Base Chemistry on the Removal of Gallium by Volatility from Weapons-Grade Plutonium Dissolved in Molten Chlorides  

Science Conference Proceedings (OSTI)

It has been proposed that GaCl{sub 3} can be removed by direct volatilization from a Pu-Ga alloy that is dissolved in a molten chloride salt. Although pure GaCl{sub 3} is quite volatile (boiling point: 201 deg. C), the behavior of GaCl{sub 3} dissolved in chloride salts is quite different because of solution effects and is critically dependent upon the composition of the solvent salt (i.e., its Lewis acid/base character). In this technical note, the behavior of gallium in prototypical Lewis acid and Lewis base salts is contrasted. It is found that gallium volatility is suppressed in basic melts and promoted in acidic melts. These results have an important influence on the potential for simple gallium removal in molten salt systems.

Williams, David F.; Cul, Guillermo D. del [Oak Ridge National Laboratory (United States); Toth, Louis M. [Electrochemical Systems (United States); Collins, Emory D. [Oak Ridge National Laboratory (United States)

2001-12-15T23:59:59.000Z

348

Universal ultracold collision rates for polar molecules of two alkali-metal atoms  

E-Print Network (OSTI)

Universal collision rate constants are calculated for ultracold collisions of two like bosonic or fermionic heteronuclear alkali-metal dimers involving the species Li, Na, K, Rb, or Cs. Universal collisions are those for which the short range probability of a reactive or quenching collision is unity such that a collision removes a pair of molecules from the sample. In this case, the collision rates are determined by universal quantum dynamics at very long range compared to the chemical bond length. We calculate the universal rate constants for reaction of the reactive dimers in their ground vibrational state $v=0$ and for vibrational quenching of non-reactive dimers with $v \\ge 1$. Using the known dipole moments and estimated van der Waals coefficients of each species, we calculate electric field dependent loss rate constants for collisions of molecules tightly confined to quasi-two-dimensional geometry by a one-dimensional optical lattice. A simple scaling relation of the quasi-two-dimensional loss rate cons...

Julienne, Paul S; Idziaszek, Zbigniew

2011-01-01T23:59:59.000Z

349

An Alkali-Vapor Cell with Metal Coated Windows for Efficient Application of an Electric Field  

E-Print Network (OSTI)

We describe the implementation of a cylindrical T-shaped alkali-vapor cell for laser spectroscopy in the presence of a longitudinal electric field. The two windows are used as two electrodes of the high-voltage assembly, which is made possible by a metallic coating which entirely covers the inner and outer sides of the windows except for a central area to let the laser beams in and out of the cell. This allows very efficient application of the electric field, up to 2 kV/cm in a rather dense superheated vapor, even when significant photoemission takes place at the windows during pulsed laser irradiation. The body of the cell is made of sapphire or alumina ceramic to prevent large currents resulting from surface conduction observed in cesiated glass cells. The technique used to attach the monocrystalline sapphire windows to the cell body causes minimal stress birefringence in the windows. In addition, reflection losses at the windows can be made very small. The vapor cell operates with no buffer gas and has no ...

Sarkisyan, D; Guena, J; Lintz, M; Bouchiat, M A; Sarkisyan, David; Gu\\'{e}na, Jocelyne; Lintz, Michel; Bouchiat, Marie-Anne

2005-01-01T23:59:59.000Z

350

DOE Issues Salt Waste Determination for the Savannah River Site |  

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

Issues Salt Waste Determination for the Savannah River Site Issues Salt Waste Determination for the Savannah River Site DOE Issues Salt Waste Determination for the Savannah River Site January 18, 2006 - 10:49am Addthis WASHINGTON, DC - The U.S. Department of Energy (DOE) today issued the waste determination for the treatment and stabilization of low activity salt-waste at the Savannah River Site allowing for significant reductions in environmental and health risks posed by the material. Stored in forty-nine underground tanks, approximately 36 million gallons of radioactive waste is left over from plutonium production during the Cold War. In addition, the department issued an amended Record of Decision and Implementation Plan to the Defense Nuclear Facilities Safety Board. "Today's announcement clears the way for the removal and treatment of this

351

Salt River Project Smart Grid Project | Open Energy Information  

Open Energy Info (EERE)

Salt River Project Smart Grid Project Salt River Project Smart Grid Project Jump to: navigation, search Project Lead Salt River Project Country United States Headquarters Location Tempe, Arizona Recovery Act Funding $56,859,359.00 Total Project Value $114,003,719.00 Coverage Area Coverage Map: Salt River Project Smart Grid Project Coordinates 33.414768°, -111.9093095° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[]}

352

DOE - Office of Legacy Management -- Penn Salt Manufacturing Co Whitemarsh  

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

Penn Salt Manufacturing Co Penn Salt Manufacturing Co Whitemarsh Research Laboratories - PA 20 FUSRAP Considered Sites Site: PENN SALT MANUFACTURING CO., WHITEMARSH RESEARCH LABORATORIES (PA.20) Eliminated from further consideration under FUSRAP Designated Name: Not Designated Alternate Name: Penn Salt Company PA.20-1 Location: Philiadelphia , Pennsylvania PA.20-1 Evaluation Year: 1987 PA.20-1 Site Operations: Conducted process studies for recovery of uranium from fluoride scrap. PA.20-1 Site Disposition: Eliminated - AEC licensed operation. Potential for residual radioactive contamination considered remote due to limited quantities and scope of operations. PA.20-2 PA.20-1 Radioactive Materials Handled: Yes Primary Radioactive Materials Handled: Uranium PA.20-1 Radiological Survey(s): None Indicated

353

Energy Department Completes Salt Coolant Material Transfer to Czech  

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

Completes Salt Coolant Material Transfer to Czech Completes Salt Coolant Material Transfer to Czech Republic for Advanced Reactor Research Energy Department Completes Salt Coolant Material Transfer to Czech Republic for Advanced Reactor Research May 20, 2013 - 12:52pm Addthis News Media Contact (202) 586-4940 PRAGUE, CZECH REPUBLIC - The U.S. Department of Energy recently joined with the U.S. Embassy in Prague and the Czech Republic's Ministry of Industry and Trade to complete the transfer of 75 kilograms of fluoride salt from the Department's Oak Ridge National Laboratory (ORNL) to the Czech Nuclear Research Institute Řež for experiments at Řež's critical test facility. This partnership builds on a strong history of U.S.-Czech energy collaboration and follows President Obama's speech in Prague in April 2009, where he laid out the importance of international

354

Surface Indicators of Geothermal Activity at Salt Wells, Nevada, USA,  

Open Energy Info (EERE)

Surface Indicators of Geothermal Activity at Salt Wells, Nevada, USA, Surface Indicators of Geothermal Activity at Salt Wells, Nevada, USA, Including Warm Ground, Borate Deposits, and Siliceous Alteration Jump to: navigation, search OpenEI Reference LibraryAdd to library Conference Paper: Surface Indicators of Geothermal Activity at Salt Wells, Nevada, USA, Including Warm Ground, Borate Deposits, and Siliceous Alteration Abstract Surface indicators of geothermal activity are often present above blind or concealed geothermal systems in the Great Basin, but their expressions are sometimes subtle. When mapped in detail, these indicators yield valuable information on the location, structural controls, and potential subsurface reservoir temperatures of geothermal fluids. An example is provided by the Salt Wells geothermal system in Churchill County, Nevada, USA, where

355

BLM Approves Salt Wells Geothermal Energy Projects | Open Energy  

Open Energy Info (EERE)

Energy Projects Energy Projects Jump to: navigation, search OpenEI Reference LibraryAdd to library Web Site: BLM Approves Salt Wells Geothermal Energy Projects Abstract Abstract unavailable. Author Colleen Sievers Published U.S. Department of the Interior- Bureau of Land Management, Carson City Field Office, Nevada, 09/28/2011 DOI Not Provided Check for DOI availability: http://crossref.org Online Internet link for BLM Approves Salt Wells Geothermal Energy Projects Citation Colleen Sievers. BLM Approves Salt Wells Geothermal Energy Projects [Internet]. 09/28/2011. Carson City, NV. U.S. Department of the Interior- Bureau of Land Management, Carson City Field Office, Nevada. [updated 2011/09/28;cited 2013/08/21]. Available from: http://www.blm.gov/nv/st/en/fo/carson_city_field/blm_information/newsroom/2011/september/blm_approves_salt.html

356

Magnetotellurics At Salt Wells Area (Bureau of Land Management, 2009) |  

Open Energy Info (EERE)

Salt Wells Area (Bureau of Land Management, 2009) Salt Wells Area (Bureau of Land Management, 2009) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Magnetotellurics At Salt Wells Area (Bureau of Land Management, 2009) Exploration Activity Details Location Salt Wells Geothermal Area Exploration Technique Magnetotellurics Activity Date 2008 - 2008 Usefulness not indicated DOE-funding Unknown Exploration Basis Vulcan increased exploration efforts in the summer and fall of 2008, during which time the company drilled two temperature gradient holes (86-15 O on Pad 1 and 17-16 O on Pad 3); conducted seismic, gravity and magnetotelluric surveys; and drilled deep exploration wells at Pads 6 and 8 and binary wells at Pads 1, 2, 4, and 7. Notes Data from these wells is proprietary, and so were unavailable for inclusion

357

Salt Wells Geothermal Energy Projects Environmental Impact Statement | Open  

Open Energy Info (EERE)

Page Page Edit with form History Facebook icon Twitter icon » Salt Wells Geothermal Energy Projects Environmental Impact Statement Jump to: navigation, search OpenEI Reference LibraryAdd to library Web Site: Salt Wells Geothermal Energy Projects Environmental Impact Statement Abstract Abstract unavailable. Author Bureau of Land Management Published U.S. Department of the Interior- Bureau of Land Management, Carson City Field Office, Nevada, 07/22/2011 DOI Not Provided Check for DOI availability: http://crossref.org Online Internet link for Salt Wells Geothermal Energy Projects Environmental Impact Statement Citation Bureau of Land Management. Salt Wells Geothermal Energy Projects Environmental Impact Statement [Internet]. 07/22/2011. Carson City, NV. U.S. Department of the Interior- Bureau of Land Management, Carson City

358

Evolution of a Mediterranean Salt Lens: Scalar Properties  

Science Conference Proceedings (OSTI)

The evolution of a Mediterranean salt lens (Meddy) over a two year period is examined. Several nondimensional numbers can be used to describe the overall decay in the structure of the Moddy. Two Rossby numbers, one using the central relative ...

Dave Hebert; Neil Oakey; Barry Ruddick

1990-09-01T23:59:59.000Z

359

Industrial use of molten nitrate/nitrite salts  

DOE Green Energy (OSTI)

Nitrate salts have been used for years as a high-temperature heat transfer medium in the chemical and metal industries. This experience is often cited as an argument for the use of these salts in large-scale solar energy systems. However, this industrial experience has not been well documented and a study was carried out to provide such information to the solar community and to determine the applicability of this data base. Seven different industrial plants were visited and the plant operators were interviewed with regard to operating history and experience. In all cases the molten salt systems operate without problems. However, it is not possible to apply the base of industrial experience directly to solar thermal energy applications because of differences in operating temperature, salt composition, alloys used, and thermal/mechanical conditions.

Carling, R.W.; Mar, R.W.

1981-12-01T23:59:59.000Z

360

Expected brine movement at potential nuclear waste repository salt sites  

SciTech Connect

The BRINEMIG brine migration code predicts rates and quantities of brine migration to a waste package emplaced in a high-level nuclear waste repository in salt. The BRINEMIG code is an explicit time-marching finite-difference code that solves a mass balance equation and uses the Jenks equation to predict velocities of brine migration. Predictions were made for the seven potentially acceptable salt sites under consideration as locations for the first US high-level nuclear waste repository. Predicted total quantities of accumulated brine were on the order of 1 m/sup 3/ brine per waste package or less. Less brine accumulation is expected at domal salt sites because of the lower initial moisture contents relative to bedded salt sites. Less total accumulation of brine is predicted for spent fuel than for commercial high-level waste because of the lower temperatures generated by spent fuel. 11 refs., 36 figs., 29 tabs.

McCauley, V.S.; Raines, G.E.

1987-08-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Salt Wells Geothermal Exploratory Drilling Program EA(DOI-BLM...  

Open Energy Info (EERE)

09142009 DOI Not Provided Check for DOI availability: http:crossref.org Online Internet link for Salt Wells Geothermal Exploratory Drilling Program EA (DOI-BLM-NV-C010-2009-...

362

Michigan Natural Gas Underground Storage Salt Caverns Capacity ...  

U.S. Energy Information Administration (EIA)

Michigan Natural Gas Underground Storage Salt Caverns Capacity (Million Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9; 1990's:

363

Meddy–Seamount Interactions: Implications for the Mediterranean Salt Tongue  

Science Conference Proceedings (OSTI)

A quasigeostrophic point vortex numerical model is used to explore interactions of eddies and seamounts. The ultimate objective of this study is to assess the role of meddy–seamount interaction as an input to Mediterranean salt tongue ...

Guohui Wang; William K. Dewar

2003-11-01T23:59:59.000Z

364

Bubbles Produced by Breaking Waves in Fresh and Salt Waters  

Science Conference Proceedings (OSTI)

A greater volume of air is entrained by breaking waves to produce many more bubbles in salt, than in fresh, water. There are, however, little differences in their sizes. These results are consistent with reported observations of whitecaps over ...

Jin Wu

2000-07-01T23:59:59.000Z

365

Molten salt electrolyte battery cell with overcharge tolerance  

SciTech Connect

A molten salt electrolyte battery having an increased overcharge tolerance employs a negative electrode with two lithium alloy phases of different electrochemical potential, one of which allows self-discharge rates which permits battery cell equalization.

Kaun, Thomas D. (New Lenox, IL); Nelson, Paul A. (Wheaton, IL)

1989-01-01T23:59:59.000Z

366

Modeling of Molten Salt Mixtures: Thermodynamic Assessment of ...  

Science Conference Proceedings (OSTI)

Presentation Title, Modeling of Molten Salt Mixtures: Thermodynamic Assessment of CeBr3 and MBr-CeBr3 Systems (M=Li, Na, K, Rb). Author(s), Yue Wu, ...

367

System Requirements Document for the Molten Salt Reactor Experiment  

Science Conference Proceedings (OSTI)

The purpose of the conversion process is to convert the {sup 233}U fluoride compounds that are being extracted from the Molten Salt Reactor Experiment (MSRE) equipment to a stable oxide for long-term storage at Bldg. 3019.

Aigner, R.D.

2000-04-01T23:59:59.000Z

368

Molten Salt Solar-Electric Experiment: Volumes 1 and 2  

Science Conference Proceedings (OSTI)

The Molten Salt Electric Experiment assembled and tested the first full-system experiment of a solar central receiver plant employing molten nitrate salt as the heat transport fluid and thermal storage medium. This report focuses on the last two phases of the project: testing/operation and evaluation. Overall project data will help utilities evaluate the central receiver concept's technical status, development requirements, and potential as a renewable source of electricity.

1990-01-03T23:59:59.000Z

369

BEDT-TFF salts with fluorinated sulfonate anions.  

Science Conference Proceedings (OSTI)

A number of layered conducting BEDT-TTF, bis(ethylenedithio)tetrathiafulvalene, salts with heavily fluorinated organosulfonate anions have been prepared and characterized. Of particular interest are the salts containing SF{sub 5}RSO{sub 3}{sup -} anions, where R is a partially fluorinated aliphatic backbone. While structurally similar --the {beta}' packing type predominates--the ground state of these salts varies from superconducting in the case of {beta}'-(BEDT-TTF){sub 2}SF{sub 5}CH{sub 2}CF{sub 2}SO{sub 3} [1] to insulating. Many of the salts with insulating ground states are metallic at room temperature, but charge localization and disproportionation over crystallographically non-equivalent sites occurs at low temperature. The organosulfonate group exhibits a propensity to bind to lithium ions, thus ternary salts incorporating Li+ into the complex anion layer are often found. The fluorophilic effect in organofluorine compounds may be exploited to form salts where the conducting BEDT-TTF layers are separated by extremely bulky anion bilayers. The crystal structure of one such system, (BEDT-TTF){sub 3}[(CF{sub 3}){sub 2}CFC{sub 2}H{sub 4}SO{sub 3}]{sub 4}(H{sub 5}O{sub 2}){sub 2}, is described here.

Geiser, U.; Schlueter, J. A.; Kini, A. M.; Wang, H. H.; Ward, B. H.; Mohtasham, J.; Gard, G. L.; Portland State Univ.

2003-01-01T23:59:59.000Z

370

Savannah River Site Salt Waste Processing Facility Technology Readiness Assessment Report  

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

Salt Waste Processing Facility Salt Waste Processing Facility Technology Readiness Assessment Report Kurt D. Gerdes Harry D. Harmon Herbert G. Sutter Major C. Thompson John R. Shultz Sahid C. Smith July 13, 2009 Prepared by the U.S. Department of Energy Washington, D.C. SRS Salt Waste Processing Facility Technology Readiness Assessment July 13, 2009 ii This page intentionally left blank SRS Salt Waste Processing Facility Technology Readiness Assessment July 13, 2009 iii SRS Salt Waste Processing Facility Technology Readiness Assessment July 13, 2009 iii Signatures SRS Salt Waste Processing Facility Technology Readiness Assessment July 13, 2009 iv This page intentionally left blank SRS Salt Waste Processing Facility

371

LIFE Materails: Molten-Salt Fuels Volume 8  

SciTech Connect

The goals of the Laser Inertial Fusion Fission Energy (LIFE) is to use fusion neutrons to fission materials with no enrichment and minimum processing and have greatly reduced wastes that are not of interest to making weapons. Fusion yields expected to be achieved in NIF a few times per day are called for with a high reliable shot rate of about 15 per second. We have found that the version of LIFE using TRISO fuel discussed in other volumes of this series can be modified by replacing the molten-flibe-cooled TRISO fuel zone with a molten salt in which the same actinides present in the TRISO particles are dissolved in the molten salt. Molten salts have the advantage that they are not subject to radiation damage, and hence overcome the radiation damage effects that may limit the lifetime of solid fuels such as TRISO-containing pebbles. This molten salt is pumped through the LIFE blanket, out to a heat exchanger and back into the blanket. To mitigate corrosion, steel structures in contact with the molten salt would be plated with tungsten or nickel. The salt will be processed during operation to remove certain fission products (volatile and noble and semi-noble fission products), impurities and corrosion products. In this way neutron absorbers (fission products) are removed and neutronics performance of the molten salt is somewhat better than that of the TRISO fuel case owing to the reduced parasitic absorption. In addition, the production of Pu and rare-earth elements (REE) causes these elements to build up in the salt, and leads to a requirement for a process to remove the REE during operation to insure that the solubility of a mixed (Pu,REE)F3 solid solution is not exceeded anywhere in the molten salt system. Removal of the REE will further enhance the neutronics performance. With molten salt fuels, the plant would need to be safeguarded because materials of interest for weapons are produced and could potentially be removed.

Moir, R; Brown, N; Caro, A; Farmer, J; Halsey, W; Kaufman, L; Kramer, K; Latkowski, J; Powers, J; Shaw, H; Turchi, P

2008-12-11T23:59:59.000Z

372

Alternative Fuels Data Center: Salt Lake City Fuels Vehicles With Natural  

Alternative Fuels and Advanced Vehicles Data Center (EERE)

Salt Lake City Fuels Salt Lake City Fuels Vehicles With Natural Gas to someone by E-mail Share Alternative Fuels Data Center: Salt Lake City Fuels Vehicles With Natural Gas on Facebook Tweet about Alternative Fuels Data Center: Salt Lake City Fuels Vehicles With Natural Gas on Twitter Bookmark Alternative Fuels Data Center: Salt Lake City Fuels Vehicles With Natural Gas on Google Bookmark Alternative Fuels Data Center: Salt Lake City Fuels Vehicles With Natural Gas on Delicious Rank Alternative Fuels Data Center: Salt Lake City Fuels Vehicles With Natural Gas on Digg Find More places to share Alternative Fuels Data Center: Salt Lake City Fuels Vehicles With Natural Gas on AddThis.com... May 14, 2011 Salt Lake City Fuels Vehicles With Natural Gas W atch how Salt Lake City fuels vehicles with liquefied and compressed

373

LITERATURE REVIEW OF BORIC ACID SOLUBILITY DATA  

SciTech Connect

A new solvent system is being evaluated for use in the Modular Caustic-Side Solvent Extraction Unit (MCU) and in the Salt Waste Processing Facility (SWPF). The new system replaces the current dilute nitric acid strip solution with 0.01 M boric acid. This literature study is performed to determine if there is a potential for boric acid to crystallize in the lines with emphasis on the transfer lines to the Defense Waste Processing Facility. This report focuses on the aqueous phase chemistry of boric acid under conditions relevant to MCU and SWPF. Operating and transfer conditions examined for the purpose of this review include temperatures between 13 C (McLeskey, 2008) and 45 C (Fondeur, 2007) and concentrations from 0 to 3M in nitric acid as well as exposure of small amounts of entrained boric acid in the organic phase to the sodium hydroxide caustic wash stream. Experiments were also conducted to observe any chemical reactions and off-gas generation that could occur when 0.01 M boric acid solution mixes with 3 M nitric acid solution and vice versa. Based on the low concentration (0.01M) of boric acid in the MCU/SWPF strip acid and the moderate operating temperatures (13 C to 45 C), it is unlikely that crystallization of boric acid will occur in the acid strip solution under process or transfer conditions. Mixing experiments of boric and nitric acid show no measurable gas generation (< 1 cc of gas per liter of solution) under similar process conditions.

Crapse, K.; Kyser, E.

2011-09-22T23:59:59.000Z

374

Assessment of the Use of Nitrogen Trifluoride for Purifying Coolant and Heat Transfer Salts in the Fluoride Salt-Cooled High-Temperature Reactor  

Science Conference Proceedings (OSTI)

This report provides an assessment of the use of nitrogen trifluoride for removing oxide and water-caused contaminants in the fluoride salts that will be used as coolants in a molten salt cooled reactor.

Scheele, Randall D.; Casella, Andrew M.

2010-09-28T23:59:59.000Z

375

Effects of alkali-metal impurities on fracture toughness of 2090 Al-Li-Cu extrusions  

Science Conference Proceedings (OSTI)

The effects of alkali-metal impurity (AMI) content, temperature, and crack-mouth-opening displacement (CMOD) rate on the fracture toughness of 2090-T8 Al-Li-Cu alloy extrusions were studied, particularly for short-transverse (S-L) orientations. Decreasing AMI content resulted in increasing room-temperature fracture toughness, especially for underaged S-L and T-L specimens. Unlike most Al-Li based alloys, material with very low (AMIs produced by vacuum refining had a high S-L fracture toughness (up to 38 MPa{radical}m for proof strengths {approximately}440 MPa) as well as high toughness in other orientations. The increase in room-temperature fracture toughness with decreasing AMI content was associated with a decrease in the proportion o brittle intergranular and cleavage-like islands, and a corresponding increase in the proportion of high energy dimpled fracture modes, on fracture surfaces. Both the present and previous studies indicate that the brittle islands result from liquid-metal embrittlement due to the presence of discrete sodium-potassium rich liquid phases. For medium to high AMI contents (5 to 37 wt ppm), S-L fracture toughness increased with decreasing temperature due to solidification of these phases and a consequent decrease in the mobility of embrittling atoms. The ability of embrittling atoms to keep up with crack tips also depended on crack velocity so that CMOD rate influenced fracture toughness. The grain structure (degree of recrystallization) appeared to be another important parameter affecting fracture toughness.

Sweet, E.D.; Bennett, C.G.; Musulin, I. [Comalco Research Centre, Thomastown, Victoria (Australia); Lynch, S.P.; Nethercott, R.B. [Defence Science and Technology Organisation, Melbourne, Victoria (Australia)

1996-11-01T23:59:59.000Z

376

Alkali-free bioactive glasses for bone tissue engineering: A preliminary investigation  

SciTech Connect

An alkali-free series of bioactive glasses has been designed and developed in the glass system CaO-MgO-SiO2-P2O5-CaF2 along diopside (CaMgSi2O6) – fluorapatite [Ca5(PO4)3F] – tricalcium phosphate (3CaO•P2O5) join. The silicate network in all the investigated glasses is predominantly coordinated in Q2 (Si) units while phosphorus tends to remain in orthophosphate (Q0) environment. The in vitro bioactivity analysis of glasses has been made by immersion of glass powders in simulated body fluid (SBF) while chemical degradation has been studied in Tris-HCl in accordance with ISO-10993-14. Some of the investigated glasses exhibit hydroxyapatite (HA) formation on their surface with in 1-12 h of their immersion in SBF solution. The sintering and crystallization kinetics of glasses has been investigated by differential thermal analysis (DTA) and hot-stage microscopy (HSM), respectively while the crystalline phase evolution in resultant glass-ceramics (GCs) has been studied in the temperature range of 800-900 oC using powder X-ray diffraction (XRD) and scanning electron microscope (SEM). The cell growth and osteogenic differentiation for glasses has been studied in vitro on sintered glass powder compacts using rat bone marrow mesenchymal stem cells. The as designed glasses are ideal candidates for their potential applications in bone tissue engineering in the form of bioactive glasses as well as glass/GC scaffolds.

Goel, Ashutosh; Kapoor, Saurabh; Rajagopal, Raghu R.; Pascual, Maria J.; Kim, Hae-Won; Ferreira, Jose M.

2011-08-25T23:59:59.000Z

377

CRITICALITY SAFETY OF PROCESSING SALT SOLUTION AT SRS  

Science Conference Proceedings (OSTI)

High level radioactive liquid waste generated as a result of the production of nuclear material for the United States defense program at the Savannah River Site has been stored as 36 million gallons in underground tanks. About ten percent of the waste volume is sludge, composed of insoluble metal hydroxides primarily hydroxides of Mn, Fe, Al, Hg, and most radionuclides including fission products. The remaining ninety percent of the waste volume is saltcake, composed of primarily sodium (nitrites, nitrates, and aluminates) and hydroxides. Saltcakes account for 30% of the radioactivity while the sludge accounts for 70% of the radioactivity. A pilot plant salt disposition processing system has been designed at the Savannah River Site for interim processing of salt solution and is composed of two facilities: the Actinide Removal Process Facility (ARPF) and the Modular Caustic Side Solvent Extraction Unit (MCU). Data from the pilot plant salt processing system will be used for future processing salt at a much higher rate in a new salt processing facility. Saltcake contains significant amounts of actinides, and other long-lived radioactive nuclides such as strontium and cesium that must be extracted prior to disposal as low level waste. The extracted radioactive nuclides will be mixed with the sludge from waste tanks and vitrified in another facility. Because of the presence of highly enriched uranium in the saltcake, there is a criticality concern associated with concentration and/or accumulation of fissionable material in the ARP and MCU.

Stephens, K; Davoud Eghbali, D; Michelle Abney, M

2008-01-15T23:59:59.000Z

378

Effect of water in salt repositories. Final report  

Science Conference Proceedings (OSTI)

Additional results confirm that during most of the consolidation of polycrystalline salt in brine, the previously proposed rate expression applies. The final consolidation, however, proceeds at a lower rate than predicted. The presence of clay hastens the consolidation process but does not greatly affect the previously observed relationship between permeability and void fraction. Studies of the migration of brine within polycrystalline salt specimens under stress indicate that the principal effect is the exclusion of brine as a result of consolidation, a process that evidently can proceed to completion. No clear effect of a temperature gradient could be identified. A previously reported linear increase with time of the reciprocal permeability of salt-crystal interfaces to brine was confirmed, though the rate of increase appears more nearly proportional to the product of sigma ..delta..P rather than sigma ..delta..P/sup 2/ (sigma is the uniaxial stress normal to the interface and ..delta..P is the hydraulic pressure drop). The new results suggest that a limiting permeability may be reached. A model for the permeability of salt-crystal interfaces to brine is developed that is reasonably consistent with the present results and may be used to predict the permeability of bedded salt. More measurements are needed, however, to choose between two limiting forms of the model.

Baes, C.F. Jr.; Gilpatrick, L.O.; Kitts, F.G.; Bronstein, H.R.; Shor, A.J.

1983-09-01T23:59:59.000Z

379

Method for making a uranium chloride salt product  

DOE Patents (OSTI)

The subject apparatus provides a means to produce UCl.sub.3 in large quantities without incurring corrosion of the containment vessel or associated apparatus. Gaseous Cl is injected into a lower layer of Cd where CdCl.sub.2 is formed. Due to is lower density, the CdCl.sub.2 rises through the Cd layer into a layer of molten LiCl--KCL salt where a rotatable basket containing uranium ingots is suspended. The CdCl.sub.2 reacts with the uranium to form UCl.sub.3 and Cd. Due to density differences, the Cd sinks down to the liquid Cd layer and is reused. The UCl.sub.3 combines with the molten salt. During production the temperature is maintained at about 600.degree. C. while after the uranium has been depleted the salt temperature is lowered, the molten salt is pressure siphoned from the vessel, and the salt product LiCl--KCl-30 mol % UCl.sub.3 is solidified.

Miller, William E. (Naperville, IL); Tomczuk, Zygmunt (Lockport, IL)

2004-10-05T23:59:59.000Z

380

Alkali injection system with controlled CO/sub 2//O/sub 2/ ratios for combustion of coal  

DOE Patents (OSTI)

A high temperature combustion process for an organic fuel containing sulfur in which the nitrogen of air is replaced by carbon dioxide for combination with oxygen with the ratio of CO/sub 2//O/sub 2/ being controlled to generate combustion temperatures above 2000/sup 0/K for a gas-gas reaction with SO/sub 2/ and an alkali metal compound to produce a sulfate and in which a portion of the carbon-dioxide rich gas is recycled for mixing with oxygen and/or for injection as a cooling gas upstream from heating exchangers to limit fouling of the exchangers, with the remaining carbon-dioxide rich gas being available as a source of CO/sub 2/ for oil recovery and other purposes. Several advantages are associated with the invention. First, by using a low CO/sub 2//O/sub 2/ ratio, higher flame temperatures can be achieved, thereby substantially promoting the gas-gas reaction between alkali atoms and sulfur gases. Second, by providing a means for injecting additional CO/sub 2/ at various locations removed from the combustion zone, the heat transfer rate and cooling of the alkali sulfates can be tightly controlled without suffering either the loss in efficiency inherent in conventional gas recycle techniques or the added cost associated with the larger mass throughput rate and heat transfer surface area. Third, there is the ability to use the concept in retrofit applications by tailoring the CO/sub 2/ quantity recycled to match the heat utilization performance previously achieved using air as the oxidizing medium. Fourth, a natural reduction in nitrous oxides is achieved by eliminating the reaction of oxygen with the nitrogen in the oxidizer.

Berry, G.F.

1986-11-21T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Performance-based approach to evaluate alkali-silica reaction potential of aggregate and concrete using dilatometer method  

E-Print Network (OSTI)

The undesirable expansion of concrete because of a reaction between alkalis and certain type of reactive siliceous aggregates, known as alkali-silica reactivity (ASR), continues to be a major problem across the entire world. The renewed interest to minimize distress resulting from ASR has emphasized the need to develop predictable modeling of concrete ASR behavior under field conditions. Current test methods are either incapable or need long testing periods in which to only offer rather limited predictive estimates of ASR behavior in a narrow and impractical band of field conditions. Therefore, an attempt has been made to formulate a robust performance approach based upon basic properties of aggregate and concrete ASR materials derived from dilatometry and a kinetic-based mathematical expressions for ASR behavior. Because ASR is largely an alkali as well as a thermally activated process, the use of rate theory (an Arrhenius relationship between temperature and the alkali solution concentration) on the dilatometer time-expansion relationship, provides a fundamental aggregate ASR material property known as “activation energy.” Activation energy is an indicator of aggregate reactivity which is a function of alkalinity, particle size, crystallinity, calcium concentration, and others. The studied concrete ASR material properties represent a combined effects of mixture related properties (e.g., water-cementitious ratio, porosity, presence of supplementary cementitious materials, etc.) and maturity. Therefore, the proposed performance-based approach provides a direct accountability for a variety of factors that affect ASR, such as aggregate reactivity (activation energy), temperature, moisture, calcium concentration, solution alkalinity, and water-cementitious material ratio. Based on the experimental results, the following conclusion can be drawn concerning the performance-based approach to evaluate ASR potential of aggregate and concrete using dilatometer method; (i) the concept of activation energy can be used to represent the reactivity of aggregate subjected to ASR, (ii) the activation energy depends on the reactivity of aggregate and phenomenological alkalinity of test solution, and (iii) The proposed performance-based model provides a means to predict ASR expansion development in concrete.

Shon, Chang Seon

2008-05-01T23:59:59.000Z

382

DOE Joint Genome Institute: Salt-loving Microbe Provides New Enzymes for  

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

June 30, 2011 June 30, 2011 Salt-loving Microbe Provides New Enzymes for the Production of Next Gen Biofuels WALNUT CREEK, Calif.-In order to realize the full potential of advanced biofuels that are derived from non-food sources of lignocellulosic biomass-e.g., agricultural, forestry, and municipal waste, and crops such as poplar, switchgrass and miscanthus-new technologies that can efficiently and cost-effectively break down this biomass into simple sugars are required. Existing biomass pretreatment technologies are typically derived from the pulp and paper industry and rely on dilute acids and bases to break down the biomass. The treated biomass product is then exposed to biological catalysts, or enzymes, to liberate the sugars. Eddy Rubin and Tao Zhang Photo:Tao Zhang (left), and Eddy Rubin (right).

383

Savannah River Site - Salt Waste Processing Facility Independent Technical Review  

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

SALT WASTE PROCESSING FACILITY SALT WASTE PROCESSING FACILITY INDEPENDENT TECHNICAL REVIEW November 22, 2006 Conducted by: Harry Harmon, Team Lead Civil/Structural Sub Team Facility Safety Sub Team Engineering Sub Team Peter Lowry, Lead James Langsted, Lead George Krauter, Lead Robert Kennedy Chuck Negin Art Etchells Les Youd Jerry Evatt Oliver Block Loring Wyllie Richard Stark Tim Adams Tom Anderson Todd LaPointe Stephen Gosselin Carl Costantino Norman Moreau Patrick Corcoran John Christian Ken Cooper Kari McDaniel _____________________________ Harry D. Harmon ITR Team Leader SPD-SWPF-217 SPD-SWPF-217: Salt Waste Processing Facility Independent Technical Review 11/22/2006 ACKNOWLEDGEMENT The ITR Team wishes to thank Shari Clifford of Pacific Northwest National Laboratory for

384

Salt Waste Processing Facility Fact Sheet | Department of Energy  

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

Services » Waste Management » Tank Waste and Waste Processing » Services » Waste Management » Tank Waste and Waste Processing » Salt Waste Processing Facility Fact Sheet Salt Waste Processing Facility Fact Sheet Nuclear material production operations at SRS resulted in the generation of liquid radioactive waste that is being stored, on an interim basis, in 49 underground waste storage tanks in the F- and H-Area Tank Farms. SWPF Fact Sheet More Documents & Publications EIS-0082-S2: Amended Record of Decision Savannah River Site Salt Waste Processing Facility Technology Readiness Assessment Report EIS-0082-S2: Record of Decision Waste Management Nuclear Materials & Waste Tank Waste and Waste Processing Waste Disposition Packaging and Transportation Site & Facility Restoration Deactivation & Decommissioning (D&D)

385

Injector nozzle for molten salt destruction of energetic waste materials  

DOE Patents (OSTI)

An injector nozzle has been designed for safely injecting energetic waste materials, such as high explosives, propellants, and rocket fuels, into a molten salt reactor in a molten salt destruction process without premature detonation or back burn in the injection system. The energetic waste material is typically diluted to form a fluid fuel mixture that is injected rapidly into the reactor. A carrier gas used in the nozzle serves as a carrier for the fuel mixture, and further dilutes the energetic material and increases its injection velocity into the reactor. The injector nozzle is cooled to keep the fuel mixture below the decomposition temperature to prevent spontaneous detonation of the explosive materials before contact with the high-temperature molten salt bath. 2 figs.

Brummond, W.A.; Upadhye, R.S.

1996-02-13T23:59:59.000Z

386

Tests of prototype salt stripper system for IFR fuel cycle  

Science Conference Proceedings (OSTI)

One of the waste treatment steps for the on-site reprocessing of spent fuel from the Integral Fast Reactor fuel cycles is stripping of the electrolyte salt used in the electrorefining process. This involves the chemical reduction of the actinides and rare earth chlorides forming metals which then dissolve in a cadmium pool. To develop the equipment for this step, a prototype salt stripper system has been installed in an engineering scale argon-filled glovebox. Pumping trails were successful in transferring 90 kg of LiCl-KCl salt containing uranium and rare earth metal chlorides at 500{degree}C from an electrorefiner to the stripper vessel at a pumping rate of about 5 L/min. The freeze seal solder connectors which were used to join sections of the pump and transfer line performed well. Stripping tests have commenced employing an inverted cup charging device to introduce a Cd-15 wt % Li alloy reductant to the stripper vessel.

Carls, E.L.; Blaskovitz, R.J.; Johnson, T.R. [Argonne National Lab., IL (United States); Ogata, T. [Central Research Inst. of Electric Power Industry, Tokyo (Japan)

1993-09-01T23:59:59.000Z

387

Injector nozzle for molten salt destruction of energetic waste materials  

DOE Patents (OSTI)

An injector nozzle has been designed for safely injecting energetic waste materials, such as high explosives, propellants, and rocket fuels, into a molten salt reactor in a molten salt destruction process without premature detonation or back burn in the injection system. The energetic waste material is typically diluted to form a fluid fuel mixture that is injected rapidly into the reactor. A carrier gas used in the nozzle serves as a carrier for the fuel mixture, and further dilutes the energetic material and increases its injection velocity into the reactor. The injector nozzle is cooled to keep the fuel mixture below the decomposition temperature to prevent spontaneous detonation of the explosive materials before contact with the high-temperature molten salt bath.

Brummond, William A. (Livermore, CA); Upadhye, Ravindra S. (Pleasanton, CA)

1996-01-01T23:59:59.000Z

388

Columbus Salt Marsh Geothermal Area | Open Energy Information  

Open Energy Info (EERE)

Columbus Salt Marsh Geothermal Area Columbus Salt Marsh Geothermal Area Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Geothermal Resource Area: Columbus Salt Marsh Geothermal Area Contents 1 Area Overview 2 History and Infrastructure 3 Regulatory and Environmental Issues 4 Exploration History 5 Well Field Description 6 Geology of the Area 7 Geofluid Geochemistry 8 NEPA-Related Analyses (0) 9 Exploration Activities (3) 10 References Area Overview Geothermal Area Profile Location: California Exploration Region: Walker-Lane Transition Zone Geothermal Region GEA Development Phase: 2008 USGS Resource Estimate Mean Reservoir Temp: Estimated Reservoir Volume: Mean Capacity: Click "Edit With Form" above to add content History and Infrastructure Operating Power Plants: 0 No geothermal plants listed.

389

Structure and dynamics in yttrium-based molten rare earth alkali fluorides  

E-Print Network (OSTI)

The transport properties of molten LiF-YF$_3$ mixtures have been studied by pulsed field gradient nuclear magnetic resonance spectroscopy, potentiometric experiments, and molecular dynamics simulations. The calculated diffusion coefficients and electric conductivities compare very well with the measurements accross a wide composition range. We then extract static (radial distribution functions, coordination numbers distributions) and dynamic (cage correlation functions) quantities from the simulations. Then, we discuss the interplay between the microscopic structure of the molten salts and their dynamic properties. It is often considered that variations in the diffusion coefficient of the anions are mainly driven by the evolution of its coordination with the metallic ion (Y$^{3+}$ here). We compare this system with fluorozirconate melts and demonstrate that the coordination number is a poor indicator of the evolution of the diffusion coefficient. Instead, we propose to use the ionic bonds lifetime. We show th...

Levesque, Maximilien; Salanne, Mathieu; Gobet, Mallory; Groult, Henri; Bessada, Catherine; Madden, Paul A; Rollet, Anne-Laure

2013-01-01T23:59:59.000Z

390

OPERATIONS REVIEW OF THE SAVANNAH RIVER SITE INTEGRATED SALT DISPOSITION PROCESS - 11327  

SciTech Connect

The Savannah River Site (SRS) is removing liquid radioactive waste from its Tank Farm. To treat waste streams that are low in Cs-137, Sr-90, and actinides, SRS developed the Actinide Removal Process and implemented the Modular Caustic Side Solvent Extraction (CSSX) Unit (MCU). The Actinide Removal Process contacts salt solution with monosodium titanate to sorb strontium and select actinides. After monosodium titanate contact, the resulting slurry is filtered to remove the monosodium titanate (and sorbed strontium and actinides) and entrained sludge. The filtrate is transferred to the MCU for further treatment to remove cesium. The solid particulates removed by the filter are concentrated to {approx} 5 wt %, washed to reduce the sodium concentration, and transferred to the Defense Waste Processing Facility for vitrification. The CSSX process extracts the cesium from the radioactive waste using a customized solvent to produce a Decontaminated Salt Solution (DSS), and strips and concentrates the cesium from the solvent with dilute nitric acid. The DSS is incorporated in grout while the strip acid solution is transferred to the Defense Waste Processing Facility for vitrification. The facilities began radiological processing in April 2008 and started processing of the third campaign ('MarcoBatch 3') of waste in June 2010. Campaigns to date have processed {approx}1.2 million gallons of dissolved saltcake. Savannah River National Laboratory (SRNL) personnel performed tests using actual radioactive samples for each waste batch prior to processing. Testing included monosodium titanate sorption of strontium and actinides followed by CSSX batch contact tests to verify expected cesium mass transfer. This paper describes the tests conducted and compares results from facility operations. The results include strontium, plutonium, and cesium removal, cesium concentration, and organic entrainment and recovery data. Additionally, the poster describes lessons learned during operation of the facility.

Peters, T.; Poirier, M.; Fondeur, F.; Fink, S.; Brown, S.; Geeting, M.

2011-02-07T23:59:59.000Z

391

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

SciTech Connect

This progress report on the Department of Energy project DE-FG-97FT97263 entitled, ''Catalytic Gasification of Coal Using Eutectic Salt Mixtures'', covers the period April-September 1998. The specific aims of the project for this period were to identify appropriate eutectic salt mixture catalysts for the gasification of Illinois No.6 coal, evaluate various impregnation or catalyst addition methods to improve catalyst dispersion, and evaluate gasification performance in a bench-scale fixed bed reactor. The project is being conducted jointly by Clark Atlanta University (CAU), the University of Tennessee Space Institute (UTSI) and the Georgia Institute of Technology (Georgia Tech) with CAU as the prime contractor. Several single salt catalysts and binary and ternary eutectic catalysts were investigated at Clark Atlanta University. Physical mixing and incipient wetness methods were investigated as catalyst addition techniques. Gasification was carried out using TGA at CAU and UTSI and with a fixed-bed reactor at UTSI. The results showed better gasification activity in the presence of the catalysts tested. The eutectic salt studies showed clear agreement between the melting points of the prepared eutectics and reported literature values. The order of catalytic activity observed was ternary > binary > single salt. With the soluble single salt catalysts, the incipient wetness method was found to give better results than physical mixing technique. Also, catalyst preparation conditions such as catalyst loading, drying time and temperature were found to influence the gasification rate. Based on the Clark Atlanta University studies on Task 1, the project team selected the 43.5%Li{sub 2}CO{sub 3}-31.5%Na{sub 2}CO{sub 3}-25%K{sub 2}CO{sub 3} ternary eutectic and the 29%Na{sub 2}CO{sub 3}-71%K{sub 2}CO{sub 3} and 2.3% KNO{sub 3}-97.7%K{sub 2}CO{sub 3} binary eutectic for the fixed bed studies at UTSI. The eutectic salts were found to be highly insoluble in aqueous medium. As a result the technique of adding the eutectic to the raw coal was found to be better than using wet methods. Also, addition of the catalyst to the raw coal appeared to give better gasification results than addition to pyrolyzed coal. In addition, eutectic catalysts added to the coal yielded better gasification rates than rates obtained by mixing the individual salts in the eutectic ratio with the coal. These results, especially with the eutectic catalysts are very significant since the use of the low melting eutectics will reduce the severity of gasification processes.

NONE

2000-04-01T23:59:59.000Z

392

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

Science Conference Proceedings (OSTI)

This progress report on the Department of Energy project DE-FG-97FT97263 entitled, ''Catalytic Gasification of Coal Using Eutectic Salt Mixtures,'' covers the period April-September 1998. The specific aims of the project for this period were to identify appropriate eutectic salt mixture catalysts for the gasification of Illinois No.6 coal, evaluate various impregnation or catalyst addition methods to improve catalyst dispersion, and evaluate gasification performance in a bench-scale fixed bed reactor. The project is being conducted jointly by Clark Atlanta University (CAU), the University of Tennessee Space Institute (UTSI) and the Georgia Institute of Technology (Georgia Tech) with CAU as the prime contractor. Several single salt catalysts and binary and ternary eutectic catalysts were investigated at Clark Atlanta University. Physical mixing and incipient wetness methods were investigated as catalyst addition techniques. Gasification was carried out using TGA at CAU and UTSI and with a fixed-bed reactor at UTSI. The results showed better gasification activity in the presence of the catalysts tested. The eutectic salt studies showed clear agreement between the melting points of the prepared eutectics and reported literature values. The order of catalytic activity observed was ternary > binary > single salt. With the soluble single salt catalysts, the incipient wetness method was found to give better results than physical mixing technique. Also, catalyst preparation conditions such as catalyst loading, drying time and temperature were found to influence the gasification rate. Based on the Clark Atlanta University studies on Task 1, the project team selected the 43.5%Li{sub 2}CO{sub 3}-31.5%Na{sub 2}CO{sub 3}-25%K{sub 2}CO{sub 3} ternary eutectic and the 29%Na{sub 2}CO{sub 3}-71%K{sub 2}CO{sub 3} and 2.3%KNO{sub 3}-97.7%K{sub 2}CO{sub 3} binary eutectic for the fixed bed studies at UTSI. The eutectic salts were found to be highly insoluble in aqueous medium. As a result the technique of adding the eutectic to the raw coal was found to be better than using wet methods. Also, addition of the catalyst to the raw coal appeared to give better gasification results than addition to pyrolyzed coal. In addition, eutectic catalysts added to the coal yielded better gasification rates than rates obtained by mixing the individual salts in the eutectic ratio with the coal. These results, especially with the eutectic catalysts are very significant since the use of the low melting eutectics will reduce the severity of gasification processes.

NONE

1998-10-01T23:59:59.000Z

393

Clean Cities Award Winning Coalition: Salt Lake City  

DOE Green Energy (OSTI)

Since its designation as a national Clean City in 1994, Salt Lake Clean Cities has put more than 2,600 alternative fuel vehicles (AFVs) on community streets. The 82 business, nonprofit, and government agencies that comprise the coalition are all dedicated to cleaning the air by reducing vehicle exhaust. Salt Lake Clean Cities has the third largest compressed natural gas and propane-refueling infrastructure in the country, with 98 locations available. They sponsor an annual ''Spring Soiree'' to increase public awareness about the program and educate the public about the benefits of alternative fuel and AFVs.

ICF Kaiser

1999-05-20T23:59:59.000Z

394

Simulation of water transport in heated rock salt  

Science Conference Proceedings (OSTI)

This paper summarizes computer simulation studies on water transport in German rock salt. Based on JOCKWERS experimental investigations on water content and water liberation, the object of these studies was to select a water transport model, that matches the water inflow which was measured in some heater experiments in the Asse Salt Mine. The main result is, that an evaporation front model, with Knudsen-type vapor transport combined with fluid transport by thermal expansion of the adsorbed water layers in the non evaporated zone, showed the best agreement with experimental evidence.

Schlich, M.; Jockwer, N.

1986-01-01T23:59:59.000Z

395

Process for making structure for a MCFC  

DOE Patents (OSTI)

A process of making a porous carbonate-containing structure for use in a molten carbonate fuel cell, wherein a suitable porous structure is prepared having disposed therein a metal salt selected from the alkali metals and the alkaline earth metals or mixtures thereof with at least a portion of the salt being a monobasic organic acid salt. The monobasic acid salt is converted to the carbonate in situ by heating in the presence of oxygen. Both electrode and electrolyte structures can be prepared. Formic acid is preferred.

Pasco, Wayne D. (Scotia, NY); Arendt, Ronald H. (Schenectady, NY)

1986-01-01T23:59:59.000Z

396

Monte Carlo simulations of electron thermalization in alkali iodide and alkaline-earth fluoride scintillators  

Science Conference Proceedings (OSTI)

A Monte Carlo model of electron thermalization in inorganic scintillators, which was developed and applied to CsI in a previous publication [Wang et al., J. Appl. Phys. 110, 064903 (2011)], is extended to another material of the alkali halide class, NaI, and to two materials from the alkaline-earth halide class, CaF2 and BaF2. This model includes electron scattering with both longitudinal optical (LO) and acoustic phonons as well as the effects of internal electric fields. For the four pure materials, a significant fraction of the electrons recombine with self-trapped holes and the thermalization distance distributions of the electrons that do not recombine peak between approximately 25 and 50 {per_thousand}nm and extend up to a few hundreds of nanometers. The thermalization time distributions of CaF2, BaF2, NaI, and CsI extend to approximately 0.5, 1, 2, and 7 ps, respectively. The simulations show that the LO phonon energy is a key factor that affects the electron thermalization process. Indeed, the higher the LO phonon energy is, the shorter the thermalization time and distance are. The thermalization time and distance distributions show no dependence on the incident {gamma}-ray energy. The four materials also show different extents of electron-hole pair recombination due mostly to differences in their electron mean free paths (MFPs), LO phonon energies, initial densities of electron-hole pairs, and static dielectric constants. The effect of thallium doping is also investigated for CsI and NaI as these materials are often doped with activators. Comparison between CsI and NaI shows that both the larger size of Cs+ relative to Na+, i.e., the greater atomic density of NaI, and the longer electron mean free path in NaI compared to CsI contribute to an increased probability for electron trapping at Tl sites in NaI versus CsI.

Wang, Zhiguo; Xie, YuLong; Campbell, Luke W.; Gao, Fei; Kerisit, Sebastien N.

2012-07-01T23:59:59.000Z

397

Monte Carlo simulations of electron thermalization in alkali iodide and alkaline-earth fluoride scintillators  

SciTech Connect

A Monte Carlo model of electron thermalization in inorganic scintillators, which was developed and applied to CsI in a previous publication [Wang et al., J. Appl. Phys. 110, 064903 (2011)], is extended to another material of the alkali halide class, NaI, and to two materials from the alkaline-earth halide class, CaF{sub 2} and BaF{sub 2}. This model includes electron scattering with both longitudinal optical (LO) and acoustic phonons as well as the effects of internal electric fields. For the four pure materials, a significant fraction of the electrons recombine with self-trapped holes and the thermalization distance distributions of the electrons that do not recombine peak between approximately 25 and 50 nm and extend up to a few hundreds of nanometers. The thermalization time distributions of CaF{sub 2}, BaF{sub 2}, NaI, and CsI extend to approximately 0.5, 1, 2, and 7 ps, respectively. The simulations show that the LO phonon energy is a key factor that affects the electron thermalization process. Indeed, the higher the LO phonon energy is, the shorter the thermalization time and distance are. The thermalization time and distance distributions show no dependence on the incident {gamma}-ray energy. The four materials also show different extents of electron-hole pair recombination due mostly to differences in their electron mean free paths (MFPs), LO phonon energies, initial densities of electron-hole pairs, and static dielectric constants. The effect of thallium doping is also investigated for CsI and NaI as these materials are often doped with activators. Comparison between CsI and NaI shows that both the larger size of Cs{sup +} relative to Na{sup +}, i.e., the greater atomic density of NaI, and the longer electron mean free path in NaI compared to CsI contribute to an increased probability for electron trapping at Tl sites in NaI versus CsI.

Wang Zhiguo; Gao Fei; Kerisit, Sebastien [Fundamental and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Xie Yulong [Energy and Environment Directorate, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Campbell, Luke W. [National Security Directorate, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States)

2012-07-01T23:59:59.000Z

398

Structural Assessment of D-Regions Affected by Alkali-Silica Reaction/Delayed Ettringite Formation  

E-Print Network (OSTI)

A combined experimental and analytical program was conducted to investigate the effects of Alkali-Silica Reaction (ASR) and Delayed Ettringite Formation (DEF) on D-regions in reinforced concrete (RC) bridge bents. Four large-scale RC specimens, which represent cantilever and straddle bents in Texas bridges in each specimen, were constructed. The first specimen represented the unexposed control specimen, while the other three were conditioned in the field with supplemental watering to promote ASR/DEF and served as the exposed specimens. The control and two exposed specimens with various levels of ASR/DEF, after eight months and two years of field conditioning, were load tested to failure. The last specimen remains in field with additional exposure to promote ASR/DEF and will be load tested in future studies. The width and length of preload-induced cracks and developing cracks that initiated in the exposed specimens and grew over time, indicating concrete expansion due to ASR/DEF mechanisms, were measured. Petrographic analysis results of concrete cores extracted from the exposed specimens after their load testing confirmed the formation of ASR gel and minimum accumulation of ettringite. The structural testing results showed that the failure mechanism in all three tested specimens was due to a brittle shear failure in the beam-column joint. However, slightly greater stiffness, strength, and ductility were observed in the exposed specimens as a result of the activation of the reinforcing steel in the specimens due to the expansion of the concrete primarily from ASR, which effectively prestressed and confined the core concrete. Sectional analysis and Strut-and-Tie Modeling (STM) of the experimental specimens were applied. Three-dimensional nonlinear Finite Element Analyses (FEA) were also conducted to numerically simulate the overall structural performance, internal response, and out-of-plane behavior of the experimental specimens. The effects of varying constitutive relations of the concrete in tension on models of the specimens were compared with the measured experimental response. A method to mimic ASR/DEF effects on exposed specimens was proposed and incorporated into the FEA approach. As a result, forces that prestress and confine the core concrete were effectively applied through the reinforcing steel prior to subsequent structural loading. The three-dimensional FEA approach was able to simulate the out-of-plane behavior of the beam-column joint and the proposed method yielded comparable results with the measured overall and internal behavior of specimens.

Liu, Shih-Hsiang 1979-

2012-12-01T23:59:59.000Z

399

Compliant alkali silicate sealing glass for solid oxide fuel cell applications: thermal cycle stability and chemical compatibility  

Science Conference Proceedings (OSTI)

An alkali silicate glass (SCN-1) is currently being evaluated as a candidate sealing glass for solid oxide fuel (SOFC) applications. The glass containing ~17 mole% alkalis (K2O and Na2O) remains vitreous and compliant during SOFC operation, unlike conventional SOFC sealing glasses, which experience substantial devitrification after the sealing process. The non-crystallizing compliant sealing glass has lower glass transition and softening temperatures since the microstructure remains glassy without significant crystallite formation, and hence can relieve or reduce residual stresses and also has the potential for crack healing. Sealing approaches based on compliant glass will also need to satisfy all the mechanical, thermal, chemical, physical, and electrical requirements for SOFC applications, not only in bulk properties but also at sealing interfaces. In this first of a series of papers we will report the thermal cycle stability of the glass when sealed between two SOFC components, i.e., a NiO/YSZ anode supported YSZ bilayer and a coated ferritic stainless steel interconnect material. High temperature leak rates were monitored versus thermal cycles between 700-850oC using back pressures ranging from 0.2 psi to 1.0 psi. Isothermal stability was also evaluated in a dual environment consisting of flowing dilute H2 fuel versus ambient air. In addition, chemical compatibility at the alumina and YSZ interfaces was examined with scanning electron microscopy and energy dispersive spectroscopy. The results shed new light on the topic of SOFC glass seal development.

Chou, Y. S.; Thomsen, Edwin C.; Williams, Riley T.; Choi, Jung-Pyung; Canfield, Nathan L.; Bonnett, Jeff F.; Stevenson, Jeffry W.; Shyam, Amit; Lara-Curzio, E.

2011-03-01T23:59:59.000Z

400

Cathodoluminescence microscopy and petrographic image analysis of aggregates in concrete pavements affected by alkali-silica reaction  

SciTech Connect

Various microscopic techniques (cathodoluminescence, polarizing and electron microscopy) were combined with image analysis with the aim to determine a) the modal composition and degradation features within concrete, and b) the petrographic characteristics and the geological types (rocks, and their provenance) of the aggregates. Concrete samples were taken from five different portions of Highway Nos. D1, D11, and D5 (the Czech Republic). Coarse and fine aggregates were found to be primarily composed of volcanic, plutonic, metamorphic and sedimentary rocks, as well as of quartz and feldspar aggregates of variable origins. The alkali-silica reaction was observed to be the main degradation mechanism, based upon the presence of microcracks and alkali-silica gels in the concrete. Use of cathodoluminescence enabled the identification of the source materials of the quartz aggregates, based upon their CL characteristics (i.e., color, intensity, microfractures, deformation, and zoning), which is difficult to distinguish only employing polarizing and electron microscopy. - Highlights: Black-Right-Pointing-Pointer ASR in concrete pavements on the Highways Nos. D1, D5 and D11 (Czech Republic). Black-Right-Pointing-Pointer Cathodoluminescence was combined with various microscopic techniques and image analysis. Black-Right-Pointing-Pointer ASR was attributed to aggregates. Black-Right-Pointing-Pointer Source materials of aggregates were identified based on cathodoluminescence characteristics. Black-Right-Pointing-Pointer Quartz comes from different volcanic, plutonic and metamorphic parent rocks.

Stastna, A., E-mail: astastna@gmail.com [Institute of Geochemistry, Mineralogy and Mineral Resources, Faculty of Science, Charles University in Prague, Albertov 6, 128 43 Praha 2 (Czech Republic); Sachlova, S.; Pertold, Z.; Prikryl, R. [Institute of Geochemistry, Mineralogy and Mineral Resources, Faculty of Science, Charles University in Prague, Albertov 6, 128 43 Praha 2 (Czech Republic); Leichmann, J. [Department of Geological Sciences, Faculty of Science, Masaryk University in Brno, Kotlarska 267/2, 611 37 Brno (Czech Republic)

2012-03-15T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Optimization and preconceptual design of a 5 MWe salt-gradient solar pond power plant at Great Salt Lake  

DOE Green Energy (OSTI)

The techniques used to optimize and design a solar salt-gradient pond (SSP) power plant for installation at the Great Salt Lake are described. The method and results of the site selection study are described as well as the characteristics of the selected site. The figure of merit used as well as the characteristics of the selected site. The figure of merit used in the optimization study, the general optimization approach, and the specific optimization method used for each subsystem are described. Results are then discussed of the optimization of the pond configuration, total system, and piping. Pond design and ground rule sensitivity studies are reported. (LEW)

Drost, M.K.; Brown, L.M.; Barnhart, J.S.; Cavola, R.G.; Hauser, S.G.; Johnson, B.M.

1983-05-01T23:59:59.000Z

402

Rapid Removal of Chlorine in Molten Salt Electrolysis of Magnesium ...  

Science Conference Proceedings (OSTI)

However, experimental data and modeling results in this study indicate that the ... bubbles on the current efficiency and the cell potential were investigated. ... High- Chloride Circuit for the Starfield Resources' Ferguson Lake Project · Direct Synthesis of Niobium Aluminides Powders by Sodiothermic Reduction in Molten Salts.

403

Lake-Breeze Fronts in the Salt Lake Valley  

Science Conference Proceedings (OSTI)

Winds at the Salt Lake City International Airport (SLC) during the April–October period from 1948 to 2003 have been observed to shift to the north (up-valley direction) between late morning and afternoon on over 70% of the days without ...

Daniel E. Zumpfe; John D. Horel

2007-02-01T23:59:59.000Z

404

Mixing in a Moderately Sheared Salt-Fingering Layer  

Science Conference Proceedings (OSTI)

Mixing due to sheared salt fingers is studied by means of direct numerical simulations (DNS) of a double-diffusively unstable shear layer. The focus is on the “moderate shear” case, where shear is strong enough to produce Kelvin–Helmholtz (KH) ...

W. D. Smyth; S. Kimura

2011-07-01T23:59:59.000Z

405

[Polymer-in-salt electrolytes]. Annual report and extension proposal  

DOE Green Energy (OSTI)

The research proposed for the current grant consisted of five components, of which the authors have made substantial progress on three and have performed some exploratory work on a sixth for which they present here an argument for extending. The components on which they have made progress are: (1) development of and improvement on the basic polymer-in-salt idea. This will be separated into parts dealing with improvements in salt constitution, and improvements in polymer type, emphasizing the role of anionic polymers; (2) modifications of the polymer-in-salt electrolyte to include the addition of solid particulates to the salt-polymer matrix; and (3) physical measurements. The new component on which they have made some preliminary measurements over the summer period concerns the use of electrolytes developed under the present and other programs for improving the performance of photovoltaic cells. The rationale is that hole/electron separation in semiconductors under irradiation is aided by trapping the holes on a redox species in an adjacent electrolyte solution. The efficiency is proportional to a number of factors not fully understood, one of which is determined by the character of the electrolyte. Since the authors have new types of electrolytes under development, and since solar energy via photovoltaic is an environmentally important aspect of the energy sciences, they felt it was a desirable aspect of materials science to study in a laboratory in Arizona. Achievements in the past year are summarized.

Angell, C.A.

1998-12-31T23:59:59.000Z

406

Solvent-free mechanochemical preparation of phosphonium salts ...  

The present invention provides a method of preparing a phosphonium salt of the formula [R.sup.1R.sup.2R.sup.3P--CR.sup.4R.sup.5R.sup.6]X, comprising ball-milling a ...

407

Marine Fog Droplets and Salt Nuclei -Part 11  

Science Conference Proceedings (OSTI)

In Past 1 of this fog study, the distribution of water with number and size of drops in some New England marine advection fogs was shown to be related to the distribution of number and size of salt particles found in marine air. It was indicated ...

Alfred H. Woodcock; Duncan C. Blanchard; James E. Jiusto

1981-01-01T23:59:59.000Z

408

Salt Lake City, Utah: Solar in Action (Brochure)  

DOE Green Energy (OSTI)

This brochure provides an overview of the challenges and successes of Salt Lake City, UT, a 2007 Solar America City awardee, on the path toward becoming a solar-powered community. Accomplishments, case studies, key lessons learned, and local resource information are given.

Not Available

2011-10-01T23:59:59.000Z

409

Separation of alcohol-water mixtures using salts  

DOE Green Energy (OSTI)

Use of a salt (KF or Na/sub 2/SO/sub 4/) to induce phase separation of alcohol-water mixtures was investigated in three process flowsheets to compare operating and capital costs with a conventional distillation process. The process feed was the Clostridia fermentation product, composed of 98 wt % water and 2 wt % solvents (70% 1-butanol, 27% 2-propanol, and 3% ethanol). The design basis was 150 x 10/sup 6/ kg/y of solvents. Phase equilibria and tieline data were obtained from literature and experiments. Three separation-process designs were developed and compared by an incremental economic analysis (+-30%) with the conventional separation technique using distillation alone. The cost of salt recovery for recycle was found to be the critical feature. High capital and operating costs make recovery of salt by precipitation uneconomical; however, a separation scheme using multiple-effect evaporation for salt recovery has comparable incremental capital costs ($1.72 x 10/sup 6/ vs $1.76 x 10/sup 6/) and lower incremental operating costs ($2.14 x 10/sup 6//y vs $4.83 x 10/sup 6//y) than the conventional separation process.

Card, J. C.; Farrell, L. M.

1982-04-01T23:59:59.000Z

410

Fabricating of Lithium-Battery-Grade Precursor Salt Cobaltous Carbonate  

Science Conference Proceedings (OSTI)

Some factors affect precursor capability, for example: raw material CoCl2 solution impurity?feeding methods of reactants?solutions’ pH value of deposition reaction?washing conditions, etc.. Cobalt chloride is chosen as raw ... Keywords: Salt Cobalt Carbonate, Cobalt Chloride, battery-grade Precursor, Shape

Jian Zhou; Li-jun Li; Gong-xiu He; Ke Chen

2010-05-01T23:59:59.000Z

411

Improved Synthesis of [Si6Cl14]2-Salts as Precursors for Si6H12and other Novel Silanes  

DOE Green Energy (OSTI)

The reaction of excess HSiCl{sub 3} with the aforementioned triamines led to the formation of [Si{sub 6}Cl{sub 14}]{sup 2-} containing salts in all instances. The isolated complex salts were characterized using FT-IR and elemental analysis. IR spectra of these compounds showed characteristic Si-H stretching modes around 2100cm{sup -1} due to the hexacoordinate silane cation and Si-Cl active modes near 528cm{sup -1} as a result of the cyclic dianion. Reaction yields and elemental analysis (CHN) of the salts are summarized in a table. The reaction of peralkylated triamines with HSiCl{sub 3} in dry CH{sub 2}Cl{sub 2} gives ionic compounds based upon the tetradecachlorocyclohexasilane dianion. Several substituted triamines(R{sub 2}NC{sub 2}H{sub 4}NR{prime}C{sub 2}H{sub 4}NR{sub 2}where R = R{prime} = Et, {sup n}Pr; R = Et, R{prime}= {sup n}Bu, {sup n}Hexyl, Benzyl) were examined for this reaction and N,N,N{prime},N{prime}-tetraethyl-N{sup {double_prime}}-benzyl-diethylenetriamine produced the best yields of [Si{sub 6}Cl{sub 14}]{sup 2-} salt at 23% based on the amine reagent. This improvement in yield could be attributed to the decreased nucleophilicity of the central amine through increased steric hindrance of the alkyl substituents. The overall consequence of this substituent variation study has revealed new reagents for the synthesis of [Si{sub 6}Cl{sub 14}]{sup 2-} salts and further demonstrated the ability of triamines to efficiently dismutate, complex, and condense chlorosilanes. The increased production of these salts has also opened a route for the study of Si{sub 6}X{sub 12} and its Lewis acid/base adducts.

Kenneth Anderson; Xuliang Dai; Kendric Nelson; Doug Schulz; Philip Boudjouk

2009-08-18T23:59:59.000Z

412

Modeling of Sulfate Double-salts in Nuclear Wastes  

Science Conference Proceedings (OSTI)

Due to limited tank space at Hanford and Savannah River, the liquid nuclear wastes or supernatants have been concentrated in evaporators to remove excess water prior to the hot solutions being transferred to underground storage tanks. As the waste solutions cooled, the salts in the waste exceeded the associated solubility limits and precipitated in the form of saltcakes. The initial step in the remediation of these saltcakes is a rehydration process called saltcake dissolution. At Hanford, dissolution experiments have been conducted on small saltcake samples from five tanks. Modeling of these experimental results, using the Environmental Simulation Program (ESP), are being performed at the Diagnostic Instrumentation and Analysis Laboratory (DIAL) at Mississippi State University. The River Protection Project (RPP) at Hanford will use these experimental and theoretical results to determine the amount of water that will be needed for its dissolution and retrieval operations. A comprehensive effort by the RPP and the Tank Focus Area continues to validate and improve the ESP and its databases for this application. The initial effort focused on the sodium, fluoride, and phosphate system due to its role in the formation of pipeline plugs. In FY 1999, an evaluation of the ESP predictions for sodium fluoride, trisodium phosphate dodecahydrate, and natrophosphate clearly indicated that improvements to the Public database of the ESP were needed. One of the improvements identified was double salts. The inability of any equilibrium thermodynamic model to properly account for double salts in the system can result in errors in the predicted solid-liquid equilibria (SLE) of species in the system. The ESP code is evaluated by comparison with experimental data where possible. However, data does not cover the range of component concentrations and temperatures found in many tank wastes. Therefore, comparison of ESP with another code is desirable, and may illuminate problems with both. For this purpose, the SOLGASMIX code was used in conjunction with a small private database developed at ORNL. This code calculates thermodynamic equilibria through minimization of Gibbs Energy, and utilizes the Pitzer model for activity coefficients. The sodium nitrate-sulfate double salt and the sodium fluoride-sulfate double salt were selected for the FY 2000 validation study of ESP. Even though ESP does not include the sulfate-nitrate double salt, this study found that this omission does not appear to be a major consequence. In this case, the solubility predictions with and without the sulfate-nitrate double salt are comparable. In contrast, even though the sulfate-fluoride double salt is included within the ESP databank, comparison to previous experimental results indicates that ESP underestimates solubility. Thus, the prediction for the sulfate-fluoride system needs to be improved. A main consequence of the inability to accurately predict the SLE of double salts is its impact on the predicted ionic strength of the solution. The ionic strength has been observed to be an important factor in the formation of pipeline plugs. To improve the ESP prediction, solubility tests on the sulfate-fluoride system are underway at DIAL, and these experimental results will be incorporated into the Public database by OLI System, Inc. Preliminary ESP simulations also indicated difficulties with the SLE prediction for anhydrous sodium sulfate. The Public database for the ESP does not include fundamental parameters for this solid in mixed solutions below 32.4 C. The limitation, in the range of anhydrous sodium sulfate, leads to convergence problems in ESP and to inaccurate predictions of solubility near the invariant point when sodium sulfate decahydrate and other salts, such as sodium nitrate, were present. These difficulties were partially corrected through the use of an additional database. In conclusion, these results indicate the need for experimental data at temperatures above 25 C and in solutions containing both nitrate and hydroxide. Furthermore, the validation and do

Toghiani, B.

2000-10-30T23:59:59.000Z

413

Deep Eutectic Salt Formulations Suitable as Advanced Heat Transfer Fluids  

Science Conference Proceedings (OSTI)

Concentrating solar power (CSP) facilities are comprised of many miles of fluid-filled pipes arranged in large grids with reflective mirrors used to capture radiation from the sun. Solar radiation heats the fluid which is used to produce steam necessary to power large electricity generation turbines. Currently, organic, oil-based fluid in the pipes has a maximum temperature threshold of 400 °C, allowing for the production of electricity at approximately 15 cents per kilowatt hour. The DOE hopes to foster the development of an advanced heat transfer fluid that can operate within higher temperature ranges. The new heat transfer fluid, when used with other advanced technologies, could significantly decrease solar electricity cost. Lower costs would make solar thermal electricity competitive with gas and coal and would offer a clean, renewable source of energy. Molten salts exhibit many desirable heat transfer qualities within the range of the project objectives. Halotechnics developed advanced heat transfer fluids (HTFs) for application in solar thermal power generation. This project focused on complex mixtures of inorganic salts that exhibited a high thermal stability, a low melting point, and other favorable characteristics. A high-throughput combinatorial research and development program was conducted in order to achieve the project objective. Over 19,000 candidate formulations were screened. The workflow developed to screen various chemical systems to discover salt formulations led to mixtures suitable for use as HTFs in both parabolic trough and heliostat CSP plants. Furthermore, salt mixtures which will not interfere with fertilizer based nitrates were discovered. In addition for use in CSP, the discovered salt mixtures can be applied to electricity storage, heat treatment of alloys and other industrial processes.

Raade, Justin; Roark, Thomas; Vaughn, John; Bradshaw, Robert

2013-07-22T23:59:59.000Z

414

Molten Salt Test Loop (MSTL) system customer interface document.  

SciTech Connect

The National Solar Thermal Test Facility at Sandia National Laboratories has a unique test capability called the Molten Salt Test Loop (MSTL) system. MSTL is a test capability that allows customers and researchers to test components in flowing, molten nitrate salt. The components tested can range from materials samples, to individual components such as flex hoses, ball joints, and valves, up to full solar collecting systems such as central receiver panels, parabolic troughs, or linear Fresnel systems. MSTL provides realistic conditions similar to a portion of a concentrating solar power facility. The facility currently uses 60/40 nitrate %E2%80%9Csolar salt%E2%80%9D and can circulate the salt at pressure up to 40 bar (600psi), temperature to 585%C2%B0C, and flow rate of 44-50kg/s(400-600GPM) depending on temperature. The purpose of this document is to provide a basis for customers to evaluate the applicability to their testing needs, and to provide an outline of expectations for conducting testing on MSTL. The document can serve as the basis for testing agreements including Work for Others (WFO) and Cooperative Research and Development Agreements (CRADA). While this document provides the basis for these agreements and describes some of the requirements for testing using MSTL and on the site at Sandia, the document is not sufficient by itself as a test agreement. The document, however, does provide customers with a uniform set of information to begin the test planning process.

Gill, David Dennis; Kolb, William J.; Briggs, Ronald D.

2013-09-01T23:59:59.000Z

415

Proceedings of 3rd US/German Workshop on Salt Repository Research, Design,  

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

Proceedings of 3rd US/German Workshop on Salt Repository Research, Proceedings of 3rd US/German Workshop on Salt Repository Research, Design, and Operation Proceedings of 3rd US/German Workshop on Salt Repository Research, Design, and Operation The 3rd U.S./German Workshop on Salt Repository Research, Design and Operation was held in Albuquerque and Carlsbad, New Mexico on October 8-11, 2012. Approximately 60 salt research scientists from Germany and the United States met to discuss repository science state of the art. Workshop topics included: 1) Safety case for heat-generating waste disposal in salt; 2) Benchmark modeling in preparation for thermomechanical field-scale tests; and 3) Reconsolidation of granular salt. Collaboration being pursued by U.S. and German salt repository researchers is presented in the report.

416

New Opportunities for Metals Extraction and Waste Treatment by Electrochemical Processing in Molten Salts  

E-Print Network (OSTI)

Molten salt electrolysis is a proven technology for the extraction of metals -- all the world's primary aluminum is produced in this manner. The unique properties of molten salts also make them

Sadoway, Donald R.

2001-01-01T23:59:59.000Z

417

How different home styles are valued in the Salt Lake City market  

E-Print Network (OSTI)

This thesis focuses on market valuation of attributes of single family housing in the Salt Lake City market. Using data from different sub-regions of Salt Lake County, this paper addresses the question of buyer demand with ...

Peterson, Barrett, 1976-

2003-01-01T23:59:59.000Z

418

Mechanisms Driving the Time-Dependent Salt Flux in a Partially Stratified Estuary  

Science Conference Proceedings (OSTI)

The subtidal salt balance and the mechanisms driving the downgradient salt flux in the Hudson River estuary are investigated using measurements from a cross-channel mooring array of current meters, temperature and conductivity sensors, and cross-...

James A. Lerczak; W. Rockwell Geyer; Robert J. Chant

2006-12-01T23:59:59.000Z

419

Design of Complex Systems to Achieve Passive Safety: Natural Circulation Cooling of Liquid Salt Pebble Bed Reactors  

E-Print Network (OSTI)

K. T. Assessment of Candidate Molten Salt Coolants for theK. T. Assessment of Candidate Molten Salt Coolants for thebeginning efforts for a molten salt reactor (MSR) program.

Scarlat, Raluca Olga

2012-01-01T23:59:59.000Z

420

Thermodynamic analysis of spent pyrochemical salts in the stored condition and in viable accident scenarios  

Science Conference Proceedings (OSTI)

This study involves examining ``spent`` electrorefining (ER) salts in the form present after usage (as stored), and then after exposure to water in a proposed accident scenario. Additionally, the equilibrium composition of the salt after extended exposure to air was also calculated by computer modeling and those results are also presented herein. It should be noted that these salts are extremely similar to spent MSE salts from the Rocky Flats MSE campaigns using NaCl-KCl- MgCl{sub 2}.

Axler, K.M.

1994-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "acids alkalies salts" 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

Structure and dynamics in yttrium-based molten rare earth alkali fluorides  

E-Print Network (OSTI)

The transport properties of molten LiF-YF3 mixtures have been studied by pulsed field gradient nuclear magnetic resonance spectroscopy, potentiometric experiments, and molecular dynamics simulations. The calculated diffusion coefficients and electric conductivities compare very well with the measurements accross a wide composition range. We then extract static (radial distribution functions, coordination numbers distributions) and dynamic (cage correlation functions) quantities from the simulations. Then, we discuss the interplay between the microscopic structure of the molten salts and their dynamic properties. It is often considered that variations in the diffusion coefficient of the anions are mainly driven by the evolution of its coordination with the metallic ion (Y3+ here). We compare this system with fluorozirconate melts and demonstrate that the coordination number is a poor indicator of the evolution of the diffusion coefficient. Instead, we propose to use the ionic bonds lifetime. We show that the weak Y-F ionic bonds in LiF-YF3 do not induce the expected tendency of the fluoride diffusion coefficient to converge toward the one of yttrium cation when the content in YF3 increases. Implications on the validity of the Nernst-Einstein relation for estimating the electrical conductivity are discussed.

Maximilien Levesque; Vincent Sarou-Kanian; Mathieu Salanne; Mallory Gobet; Henri Groult; Catherine Bessada; Paul A. Madden; Anne-Laure Rollet

2013-02-19T23:59:59.000Z

422

Precision Measurements of Atomic Lifetimes and Hyperfine Energies in Alkali Like Systems  

Science Conference Proceedings (OSTI)

Financial support of this research project has lead to advances in the study of atomic structure through precision measurements of atomic lifetimes, energy splittings, and transitions energies. The interpretation of data from many areas of physics and chemistry requires an accurate understanding of atomic structure. For example, scientists in the fields of astrophysics, geophysics, and plasma fusion depend on transition strengths to determine the relative abundances of elements. Assessing the operation of discharges and atomic resonance line filters also depends on accurate knowledge of transition strengths. Often relative transition strengths are measured precisely, but accurate atomic lifetimes are needed to obtain absolute values. Precision measurements of atomic lifetimes and energy splittings also provide fundamentally important atomic structure information. Lifetimes of allowed transitions depend most strongly on the electronic wave function far from the nucleus. Alternatively, hyperfine splittings give important information about the electronic wave function in the vicinity of the nucleus as well as the structure of the nucleus. Our main focus throughout this project has been the structure of atomic cesium because of its connection to the study of atomic parity nonconservation (PNC). The interpretation of atomic PNC experiments in terms of weak interaction coupling constants requires accurate knowledge of the electronic wave function near the nucleus as well as far from the nucleus. It is possible to address some of these needs theoretically with sophisticated many-electron atomic structure calculations. However, this program has been able to address these needs experimentally with a precision that surpasses current theoretical accuracy. Our measurements also play the important role of providing a means for testing the accuracy of many-electron calculations and guiding further theoretical development, Atomic systems such as cesium, with a single electron outside of a closed shell, provide the simplest open shell systems for detailed comparisons between experiment and theory. This program initially focused on measurements of excited state atomic lifetimes in alkali atomic systems. Our first measurements of atomic lifetimes in cesium surpassed the precision and accuracy of previous measurements and sparked renewed interest in the need for greater precision in lifetime measurements throughout the atomic physics community. After enhancing the capabilities of the laser systems built for these initial measurements, we began a study hyperfine energy splittings in cesium using a thermal atomic beam. The results surpassed previous measurements by more than an order of magnitude and lead to the first observation of the nuclear magnetic octupole moment in cesium demonstrating the inadequacy of the nuclear shell model for predicting high order nuclear moments. The laser system and atomic beam apparatus developed for these endeavors turned out to be perfectly suited for exploring the possibility of making absolute optical frequency measurements of atomic transitions. We initiated collaboration with researchers at NIST so that the desired optical frequencies could be reference with respect to the primary microwave frequency standard (Cs atomic fountain NIST-FI) via a femtosecond laser frequency comb. Our first absolute optical frequency measurement, of the cesium D2 line, surpassed the accuracy of a previous measurement by more than an order of magnitude. An absolute optical frequency measurement of the cesium D1 line, now near completion, also surpasses previous results and places us in a position to be able to report a new value for the fine structure constant which is the fundamental dimensionless constant that underlies all electromagnetic interactions.

Tanner, Carol E.

2005-03-04T23:59:59.000Z

423

Sample Results from the Interim Salt Disposition Program Macrobatch 6 Tank 21H Qualification Samples  

SciTech Connect

Savannah River National Laboratory (SRNL) analyzed samples from Tank 21H in support of qualification of Macrobatch (Salt Batch) 6 for the Interim Salt Disposition Project (ISDP). This document reports partial results of the analyses of samples of Tank 21H. No issues with the projected Salt Batch 6 strategy are identified.

Peters, T. B.; Fink, S. D.

2012-12-11T23:59:59.000Z

424

Sample Results From The Interim Salt Disposition Program Macrobatch 6 Tank 21H Qualification Samples  

Science Conference Proceedings (OSTI)

Savannah River National Laboratory (SRNL) analyzed samples from Tank 21H in support of qualification of Macrobatch (Salt Batch) 6 for the Interim Salt Disposition Project (ISDP). This document reports partial results of the analyses of samples of Tank 21H. No issues with the projected Salt Batch 6 strategy are identified.

Peters, T. B.; Fink, S. D.

2012-12-20T23:59:59.000Z

425

Bases, Assumptions, and Results of the Flowsheet Calculations for the Decision Phase Salt Disposition Alternatives  

SciTech Connect

The HLW salt waste (salt cake and supernate) now stored at the SRS must be treated to remove insoluble sludge solids and reduce the soluble concentration of radioactive cesium radioactive strontium and transuranic contaminants (principally Pu and Np). These treatments will enable the salt solution to be processed for disposal as saltstone, a solid low-level waste.

Elder, H.H.

2001-07-11T23:59:59.000Z

426

Temperature-dependent mechanical property testing of nitrate thermal storage salts.  

DOE Green Energy (OSTI)

Three salt compositions for potential use in trough-based solar collectors were tested to determine their mechanical properties as a function of temperature. The mechanical properties determined were unconfined compressive strength, Young's modulus, Poisson's ratio, and indirect tensile strength. Seventeen uniaxial compression and indirect tension tests were completed. It was found that as test temperature increases, unconfined compressive strength and Young's modulus decreased for all salt types. Empirical relationships were developed quantifying the aforementioned behaviors. Poisson's ratio tends to increase with increasing temperature except for one salt type where there is no obvious trend. The variability in measured indirect tensile strength is large, but not atypical for this index test. The average tensile strength for all salt types tested is substantially higher than the upper range of tensile strengths for naturally occurring rock salts. Interest in raising the operating temperature of concentrating solar technologies and the incorporation of thermal storage has motivated studies on the implementation of molten salt as the system working fluid. Recently, salt has been considered for use in trough-based solar collectors and has been shown to offer a reduction in levelized cost of energy as well as increasing availability (Kearney et al., 2003). Concerns regarding the use of molten salt are often related to issues with salt solidification and recovery from freeze events. Differences among salts used for convective heat transfer and storage are typically designated by a comparison of thermal properties. However, the potential for a freeze event necessitates an understanding of salt mechanical properties in order to characterize and mitigate possible detrimental effects. This includes stress imparted by the expanding salt. Samples of solar salt, HITEC salt (Coastal Chemical Co.), and a low melting point quaternary salt were cast for characterization tests to determine unconfined compressive strength, indirect tensile strength, coefficient of thermal expansion (CTE), Young's modulus, and Poisson's ratio. Experiments were conducted at multiple temperatures below the melting point to determine temperature dependence.

Everett, Randy L.; Iverson, Brian D.; Broome, Scott Thomas; Siegel, Nathan Phillip; Bronowski, David R.

2010-09-01T23:59:59.000Z

427

Kinetics of Moisture Absorption for Alkali Extracted Steam-Exploded Fiber Filled High-Density Polyethylene Composites  

Science Conference Proceedings (OSTI)

Acacia mangium wood fiber derived from steam-explosion and fiber fractionation treatment was used as fillers for high-density polyethylene (HDPE). The alkali extracted steam-exploded fibers (AEF) obtained were acetylated to produce acetylated fibers (AAEF) having three different weight percent gain (WPG). Composites of AEF or AAEF and HDPE were prepared via 2-roll mill, compression molded and cut into dumbbell specimens. All samples were immersed in water at room temperature for 30 days. The process of absorption of water by all composites followed the kinetics and mechanisms described by the Fick's theory. Diffusion coefficient (D) values increased with filler loading but decreased with increasing WPG of the AAEF fiber. Further decrease was observed when maleated polyethylene (MAPE) was added to the composite system. This was due to improved fiber-matrix adhesion that restricts movement of water molecules from further penetrate inside the composite structures.

Taib, R. M.; Ramarad, S.; Ishak, Z. A. M. [School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 11800 Minden, Pulau Pinang (Malaysia); Rozman, H. D. [School of Industrial Technology, Universiti Sains Malaysia, 11800 Minden, Pulau Pinang (Malaysia)

2010-03-11T23:59:59.000Z

428

Calculation of activities and solubilities of alkali metal perchlorates at high ionic strengths in multicomponent aqueous systems  

Science Conference Proceedings (OSTI)

The equations of Nyvlt, of Bromley, and of Pitzer for the representation of activity coefficients of electrolytes in multicomponent ionic systems have been used to fit solubility data for some alkali metal perchlorates and ammonium perchlorate in mixture with other electrolytes at ionic strengths varying from 0.08 mol-kg/sup -1/ to as high as 24 mol-kg/sup -1/. Only the Pitzer equations can be used reliably to fit the solubility data over the whole range of ionic strengths encountered for ternary systems but there are certain limitations and certain assumptions which have to be made concerning the Pitzer ionic interaction parameters. A method is also proposed for the calculation of the Pitzer single electrolyte parameters, ..beta../sup 0/, ..beta../sup 1/, and C/sup phi/, for the less soluble perchlorates from fitting their solubility data over a wide range of high ionic strengths.

Chan, C.; Khoo, K.H.

1988-06-01T23:59:59.000Z

429

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

430

Alkali injection system with controlled CO.sub.2 /O.sub.2 ratios for combustion of coal  

DOE Patents (OSTI)

A high temperature combustion process for an organic fuel containing sulfur n which the nitrogen of air is replaced by carbon dioxide for combination with oxygen with the ratio of CO.sub.2 /O.sub.2 being controlled to generate combustion temperatures above 2000 K. for a gas-gas reaction with SO.sub.2 and an alkali metal compound to produce a sulfate and in which a portion of the carbon-dioxide rich gas is recycled for mixing with oxygen and/or for injection as a cooling gas upstream from heating exchangers to limit fouling of the exchangers, with the remaining carbon-dioxide rich gas being available as a source of CO.sub.2 for oil recovery and other purposes.

Berry, Gregory F. (Naperville, IL)

1988-01-01T23:59:59.000Z

431

Preparation and evaluation of electrocatelysts for phosphoric acid fuel cells  

DOE Green Energy (OSTI)

Highly dispersed platinum has been placed on carbon supports so that they may be used as phosphoric acid fuel cell electrocatalysts. These catalysts were characterized for both the platinum surface areas and crystallite sizes. For a given carbon impregnation technique with the noble metal salt, a definite correlation between the specific surface area of the derived platinum crystallites to the BET surface area of the carbon support was found.

Jalan, V M

1978-01-01T23:59:59.000Z

432

On-sun test results from second-generation and advanced-concepts alkali-metal pool-boiler receivers  

DOE Green Energy (OSTI)

Two 75-kW{sub t} alkali-metal pool-boiler solar receivers have been successfully tested at Sandia National Laboratories` National Solar Thermal Test Facility. The first one, Sandia`s `` second-generation pool-boiler receiver,`` was designed to address commercialization issues identified during post-test assessment of Sandia`s first-generation pool-boiler receiver. It was constructed from Haynes alloy 230 and contained the alkali-metal alloy NaK-78. The absorber`s wetted side had a brazed-on powder-metal coating to stabilize boiling. This receiver was evaluated for boiling stability, hot- and warm-restart behavior, and thermal efficiency. Boiling was stable under all conditions. All of the hot restarts were successful. Mild transient hot spots observed during some hot restarts were eliminated by the addition of 1/3 torr of xenon to the vapor space. All of the warm restarts were also successful. The heat-transfer crisis that damaged the first receiver did not recur. Thermal efficiency was 92.3% at 750{degrees}C with 69.6 kW{sub t} solar input. The second receiver tested, Sandia`s ``advanced-concepts receiver,`` was a replica of the first-generation receiver except that the cavities, which were electric-discharge-machined in the absorber for boiling stability, were eliminated. This step was motivated by bench-scale test results that showed that boiling stability improved with increased heated-surface area, tilt of the heated surface from vertical, and added xenon. The bench-scale results suggested that stable boiling might be possible without heated-surface modification in a 75-kW{sub t} receiver. Boiling in the advanced-concepts receiver with 1/3 torr of xenon added has been stable under all conditions, confirming the bench-scale tests.

Moreno, J.B.; Andraka, C.E.; Moss, T.A.; Cordeiro, P.G.; Dudley, V.E.; Rawlinson, K.S.

1994-05-01T23:59:59.000Z

433

Desalination of salt water by solar energy means  

SciTech Connect

Desalination apparatus using solar energy comprises a main insulated container with a subsidiary preheating container next to it; the main container is covered with a transparent cover serving as a selective filter to provide the greenhouse effect and also as a condensation surface for water vapor, and this transparent cover incorporates a hollow space, for example by making the cover double skinned. The hollow space forms part of a syphon which automatically regulates the water levels, transferring salt water from a preheating container to the main container as the level in the main container falls due to loss by evaporation leading to condensation and withdrawal of the desalinated water. The hollow part of the transparent cover thus serves also to preheat the incoming salt water with the heat lost upon condensation by the vapor within the main container.