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Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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.


1

Chloride 2011  

Science Conference Proceedings (OSTI)

Aug 2, 2010 ... Recovery of Precious Metals from Chloride Media Using Microalgae Waste from Biofuel Extraction · Segregation Roasting of a Saprolitic ...

2

The Risk Assessment Information System  

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

Condensed Toxicity Summary for METHYLENE CHLORIDE Condensed Toxicity Summary for METHYLENE CHLORIDE NOTE: Although the toxicity values presented in these toxicity profiles were correct at the time they were produced, these values are subject to change. Users should always refer to the Toxicity Value Database for the current toxicity values. September 1993 Prepared by Cheryl B. Bast, Ph.D., Chemical Hazard Evaluation and Communication Program, Biomedical and Environmental Information Analysis Section, Health Sciences Research Division, *, Oak Ridge, Tennessee. Prepared for OAK RIDGE RESERVATION ENVIRONMENTAL RESTORATION PROGRAM. *Managed by Martin Marietta Energy Systems, Inc., for the U.S. Department of Energy under contract No. DE-AC05-84OR21400. Methylene chloride (CH2Cl2, CAS No. 75-09-2), also known as dichloromethane

3

Atmospheric Methyl Chloride  

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

steel flasks and methyl chloride concentrations were measured using an Electron Capture Gas Chromatograph. Concentrations are reported as mixing ratios in dry air. The...

4

Chloride removal from vitrification offgas  

Science Conference Proceedings (OSTI)

This study identified and investigated techniques of selectively purging chlorides from the low-level waste (LLW) vitrification process with the purge stream acceptable for burial on the Hanford Site. Chlorides will be present in high concentration in several individual feeds to the LLW Vitrification Plant. The chlorides are highly volatile in combustion type melters and are readily absorbed by wet scrubbing of the melter offgas. The Tank Waste Remediation System (TWRS) process flow sheets show that the resulting chloride rich scrub solution is recycled back to the melter. The chlorides must be purged from the recycle loop to prevent the buildup of excessively high chloride concentrations.

Slaathaug, E.J. [Westinghouse Hanford Co., Richland, WA (United States)

1995-06-01T23:59:59.000Z

5

Virtual Rapid Chloride Permeability Test  

Science Conference Proceedings (OSTI)

... final temperature can be manually copied to the final temperature in the test conditions box ... Type of software: Virtual testing of chloride permeability. ...

2013-06-11T23:59:59.000Z

6

Chloride Metallurgy: Process Technology Development  

Science Conference Proceedings (OSTI)

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

7

Process for removing halogenated aliphatic and aromatic compounds from petroleum products. [Polychlorinated biphenyls; methylene chloride; perchloroethylene; trichlorofluoroethane; trichloroethylene; chlorobenzene  

DOE Patents (OSTI)

A process for removing halogenated aliphatic and aromatic compounds, e.g., polychlorinated biphenyls, from petroleum products by solvent extraction. The halogenated aliphatic and aromatic compounds are extracted from a petroleum product into a polar solvent by contracting the petroleum product with the polar solvent. The polar solvent is characterized by a high solubility for the extracted halogenated aliphatic and aromatic compounds, a low solubility for the petroleum product and considerable solvent power for polyhydroxy compound. The preferred polar solvent is dimethylformamide. A miscible polyhydroxy compound, such as, water, is added to the polar extraction solvent to increase the polarity of the polar extraction solvent. The halogenated aliphatic and aromatic compounds are extracted from the highly-polarized mixture of polyhydroxy compound and polar extraction solvent into a low polar or nonpolar solvent by contacting the polyhydroxy compound-polar solvent mixture with the low polar or nonpolar solvent. The halogenated aliphatic and aromatic compounds in the low polar or nonpolar solvent by physical means, e.g., vacuum evaporation. The polar and nonpolar solvents are recovered for recycling. The process can easily be designed for continuous operation. Advantages of the process include that the polar solvent and a major portion of the nonpolar solvent can be recycled, the petroleum products are reclaimable and the cost for disposing of waste containing polychlorinated biphenyls is significantly reduced. 2 tables.

Googin, J.M.; Napier, J.M.; Travaglini, M.A.

1982-03-31T23:59:59.000Z

8

Chloride removal from plutonium alloy  

Science Conference Proceedings (OSTI)

SRP is evaluating a program to recover plutonium from a metallic alloy that will contain chloride salt impurities. Removal of chloride to sufficiently low levels to prevent damaging corrosion to canyon equipment is feasible as a head-end step following dissolution. Silver nitrate and mercurous nitrate were each successfully used in laboratory tests to remove chloride from simulated alloy dissolver solution containing plutonium. Levels less than 10 ppM chloride were achieved in the supernates over the precipitated and centrifuged insoluble salts. Also, less than 0.05% loss of plutonium in the +3, +4, or +6 oxidation states was incurred via precipitate carrying. These results provide impetus for further study and development of a plant-scale process to recover plutonium from metal alloy at SRP.

Holcomb, H.P.

1983-01-01T23:59:59.000Z

9

CHLORIDE WASHER PERFORMACE TESTING  

SciTech Connect

Testing was performed to determine the chloride (Cl-) removal capabilities of the Savannah River National Laboratory (SRNL) designed and built Cl- washing equipment intended for HB-Line installation. The equipment to be deployed was tested using a cerium oxide (CeO2) based simulant in place of the 3013 plutonium oxide (PuO2) material. Two different simulant mixtures were included in this testing -- one having higher Cl- content than the other. The higher Cl- simulant was based on K-Area Interim Surveillance Inspection Program (KIS) material with Cl- content approximately equal to 70,000 ppm. The lower Cl- level simulant was comparable to KIS material containing approximately 8,000-ppm Cl- content. The performance testing results indicate that the washer is capable of reducing the Cl- content of both surrogates to below 200 ppm with three 1/2-liter washes of 0.1M sodium hydroxide (NaOH) solution. Larger wash volumes were used with similar results - all of the prescribed test parameters consistently reduced the Cl- content of the surrogate to a value below 200 ppm Cl- in the final washed surrogate material. The washer uses a 20-micron filter to retain the surrogate solids. Tests showed that 0.16-0.41% of the insoluble fraction of the starting mass passed through the 20-micron filter. The solids retention performance indicates that the fissile masses passing through the 20-micron filter should not exceed the waste acceptance criteria for discard in grout to TRU waste. It is recommended that additional testing be pursued for further verification and optimization purposes. It is likely that wash volumes smaller than those tested could still reduce the Cl- values to acceptable levels. Along with reduced wash volumes, reuse of the third wash volume (in the next run processed) should be tested as a wash solution minimization plan. A 67% reduction in the number of grouted paint pails could be realized if wash solution minimization testing returned acceptable results.

Coughlin, J; David Best, D; Robert Pierce, R

2007-11-30T23:59:59.000Z

10

An Exocyclic Methylene Group Acts As a Bioisostere of the 2?-Oxygen Atom in LNA  

DOE Green Energy (OSTI)

We show for the first time that it is possible to obtain LNA-like (Locked Nucleic Acid 1) binding affinity and biological activity with carbocyclic LNA (cLNA) analogs by replacing the 2{prime}-oxygen atom in LNA with an exocyclic methylene group. Synthesis of the methylene-cLNA nucleoside was accomplished by an intramolecular cyclization reaction between a radical at the 2{prime}-position and a propynyl group at the C-4{prime} position. Only methylene-cLNA modified oligonucleotides showed similar thermal stability and mismatch discrimination properties for complementary nucleic acids as LNA. In contrast, the close structurally related methyl-cLNA analogs showed diminished hybridization properties. Analysis of crystal structures of cLNA modified self-complementary DNA decamer duplexes revealed that the methylene group participates in a tight interaction with a 2{prime}-deoxyribose residue of the 5{prime}-terminal G of a neighboring duplex, resulting in the formation of a CH...O type hydrogen bond. This indicates that the methylene group retains a negative polarization at the edge of the minor groove in the absence of a hydrophilic 2{prime}-substituent and provides a rationale for the superior thermal stability of this modification. In animal experiments, methylene-cLNA antisense oligonucleotides (ASOs) showed similar in vivo activity but reduced toxicity as compared to LNA ASOs. Our work highlights the interchangeable role of oxygen and unsaturated moieties in nucleic acid structure and emphasizes greater use of this bioisostere to improve the properties of nucleic acids for therapeutic and diagnostic applications.

Seth, Punit P.; Allerson, Charles R.; Berdeja, Andres; Siwkowski, Andrew; Pallan, Pradeep S.; Gaus, Hans; Prakash, Thazha P.; Watt, Andrew T.; Egli, Martin; Swayze, Eric E. (Isis Pharm.); (Vanderbilt)

2010-12-07T23:59:59.000Z

11

Photo-degradation of methylene blue using Ta-doped ZnO nanoparticle  

SciTech Connect

A photocatalyst of Ta-doped ZnO was prepared by a modified Pechini-type method. The structural, morphological properties and photocatalytic activity of 1 mol % Ta-doped ZnO samples annealed at different temperatures were characterized. The photo-oxidation of methylene blue under the visible-light irradiation followed the pseudo-first-order kinetics according to the Langmuir-Hinshelwood model. It is found that the photocatalysis of 1% Ta-doped ZnO annealed at 700 {sup o}C showed excellent performance of the photodegradation of methylene blue, which was attributed to a competitive trade-off among the crystallinity, surface hydroxyl groups, and specific surface area. The processing parameter such as the pH value also played an important role in tuning the photocatalytic activity. The maximum photodecomposed rate was achieved at pH=8, and an novel model about the absorption of methylene blue on the surface of the catalysts was proposed. - Graphical abstract: This model describes the adsorption between the amphoteric behavior of the metal oxide and the cationic dye methylene blue (MB) on the surface of the catalyst at the acidic and alkaline condition.

Kong Jizhou [National Laboratory of Solid State Microstructures, Materials Science and Engineering Department, Nanjing University, Nanjing 210093 (China); Li Aidong, E-mail: adli@nju.edu.c [National Laboratory of Solid State Microstructures, Materials Science and Engineering Department, Nanjing University, Nanjing 210093 (China); Li Xiangyu; Zhai Haifa; Zhang Wenqi; Gong Youpin; Li Hui; Wu Di [National Laboratory of Solid State Microstructures, Materials Science and Engineering Department, Nanjing University, Nanjing 210093 (China)

2010-06-15T23:59:59.000Z

12

Method for the abatement of hydrogen chloride  

DOE Patents (OSTI)

A method is described for reducing the amount of hydrogen chloride contained in a gas stream by reacting the hydrogen chloride with ammonia in the gas phase so as to produce ammonium chloride. The combined gas stream is passed into a condensation and collection vessel, and a cyclonic flow is created in the combined gas stream as it passes through the vessel. The temperature of the gas stream is reduced in the vessel to below the condensation temperature of ammonium chloride in order to crystallize the ammonium chloride on the walls of the vessel. The cyclonic flow creates a turbulence which breaks off the larger particles of ammonium chloride which are, in turn, driven to the bottom of the vessel where the solid ammonium chloride can be removed from the vessel. The gas stream exiting from the condensation and collection vessel is further cleaned and additional ammonium chloride is removed by passing through additional filters.

Winston, S.J.; Thomas, T.R.

1975-11-14T23:59:59.000Z

13

Microbial reductive dehalogenation of vinyl chloride  

DOE Patents (OSTI)

Compositions and methods are provided that relate to the bioremediation of chlorinated ethenes, particularly the bioremediation of vinyl chloride by Dehalococcoides-like organisms. An isolated strain of bacteria, Dehalococcoides sp. strain VS, that metabolizes vinyl chloride is provided; the genetic sequence of the enzyme responsible for vinyl chloride dehalogenation; methods of assessing the capability of endogenous organisms at an environmental site to metabolize vinyl chloride; and a method of using the strains of the invention for bioremediation.

Spormann, Alfred M. (Stanford, CA); Muller, Jochen A. (Baltimore, MD); Rosner, Bettina M. (Berlin, DE); Von Abendroth, Gregory (Nannhein, DE); Meshulam-Simon, Galit (Los Altos, CA); McCarty, Perry L (Stanford, CA)

2011-11-22T23:59:59.000Z

14

Enhanced Chloride Monitoring for Steam Condensate Samples  

Science Conference Proceedings (OSTI)

The objective of this project was to develop to the proof-of-concept stage a system that enables the quantification of chloride (Cl) in turbine steam condensate samples. The chloride quantification system is intended to serve as an alternative to online chromatography for chloride concentration monitoring. The conceptual approach was to concentrate the ions in the steam condensate, by a predetermined factor, to a level that allowed accurate detection of chloride by ion selective electrodes (ISEs). The ab...

2012-01-31T23:59:59.000Z

15

REMOVAL OF CHLORIDE FROM AQUEOUS SOLUTIONS  

DOE Patents (OSTI)

The removal of chlorides from aqueons solutions is described. The process involves contacting the aqueous chloride containing solution with a benzene solution about 0.005 M in phenyl mercuric acetate whereby the chloride anions are taken up by the organic phase and separating the organic phase from the aqueous solutions.

Schulz, W.W.

1959-08-01T23:59:59.000Z

16

Modeling acid-gas generation from boiling chloride brines  

E-Print Network (OSTI)

distillation of a calcium-chloride-dominant brine was simulateddistillation of a calcium-chloride-dominated brine is then simulated

Zhang, Guoxiang

2010-01-01T23:59:59.000Z

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

Irreversible gettering of thionyl chloride  

DOE Green Energy (OSTI)

The authors have successfully demonstrated the irreversible gettering of SOCl{sub 2} by ZnO/ASZMTEDA carbon over a modest temperature range. While thionyl chloride decomposition was slow below {minus}20 C, lower temperatures are expected to be less of a problem than at higher temperatures. The approximately 30 cc of thionyl chloride in a typical D-cell would require 50 g of ZnO and 107 g of ASZMTEDA carbon. Fortunately, since it is unlikely to happen at all, it is common practice to assume only one cell will fail (leak) in a given battery pack. So, one charge of getter can protect the whole battery pack. In summary, ZnO/ASZMTEDA carbon fulfills all of the requirements of an ideal getter including: irreversible binding or reaction with SOCl{sub 2}, high volumetric uptake capacity, high efficiency, non-volatile, air stable, insensitive to poisoning, non-toxic, cheap, non-corrosive, and the gettering product is not a liquid or oil that could block further flow or accessibility. Future work in this area includes incorporation of the ZnO and carbon into a structural open-celled porous monolith, as well as, gettering for other types of batteries (e.g., Li/MnO{sub 2}).

LeRoy Whinnery; Steve Goods; George Buffleben; Tim Sheppodd

1999-11-01T23:59:59.000Z

19

Chloride substitution in sodium borohydride  

Science Conference Proceedings (OSTI)

The dissolution of sodium chloride and sodium borohydride into each other resulting in formation of solid solutions of composition Na(BH{sub 4}){sub 1-x}Cl{sub x} is studied. The dissolution reaction is facilitated by two methods: ball milling or combination of ball milling and annealing at 300 deg. C for three days of NaBH{sub 4}-NaCl samples in molar ratios of 0.5:0.5 and 0.75:0.25. The degree of dissolution is studied by Rietveld refinement of synchrotron radiation powder X-ray diffraction (SR-PXD) data. The results show that dissolution of 10 mol% NaCl into NaBH{sub 4}, forming Na(BH{sub 4}){sub 0.9}Cl{sub 0.1}, takes place during ball milling. A higher degree of dissolution of NaCl in NaBH{sub 4} is obtained by annealing resulting in solid solutions containing up to 57 mol% NaCl, i.e. Na(BH{sub 4}){sub 0.43}Cl{sub 0.57}. In addition, annealing results in dissolution of 10-20 mol% NaBH{sub 4} into NaCl. The mechanism of the dissolution during annealing and the decomposition pathway of the solid solutions are studied by in situ SR-PXD. Furthermore, the stability upon hydrogen release and uptake were studied by Sieverts measurements. - Graphical Abstract: Dissolution of sodium chloride and sodium borohydride into each other resulting in formation of solid solutions of composition Na(BH{sub 4}){sub 1-x}Cl{sub x} is studied. Dissolution is facilitated by two methods: ball milling or annealing at 300 deg. C for three days of NaBH{sub 4}-NaCl samples. Sample compositions and dissolution mechanism are studied by Rietveld refinement of synchrotron radiation powder X-ray diffraction data. Highlights: > Studies of dissolution of sodium chloride and sodium borohydride into each other. > Solid state diffusion facilitated by mechanical and thermal treatments. > Dissolution is more efficiently induced by heating than by mechanical treatment. > Mechanism for dissolution studied by Rietveld refinement of in situ SR-PXD data.

Ravnsbaek, Dorthe B.; Rude, Line H. [Center for Materials Crystallography (CMC), Interdisciplinary Nanoscience Center (iNANO), Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Arhus C (Denmark); Jensen, Torben R., E-mail: trj@chem.au.dk [Center for Materials Crystallography (CMC), Interdisciplinary Nanoscience Center (iNANO), Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Arhus C (Denmark)

2011-07-15T23:59:59.000Z

20

Process for synthesis of beryllium chloride dietherate  

DOE Green Energy (OSTI)

A low temperature method of producing beryllium chloride dietherate through the addition of hydrogen chloride gas to a mixture of beryllium metal in ether in a reaction vessel is described. A reflux condenser provides an exit for hydrogen produced form the reaction. A distillation condenser later replaces the reflux condenser for purifying the resultant product.

Bergeron, Charles (Baton Rouge, LA); Bullard, John E. (Kendall Park, NJ); Morgan, Evan (Lynchburg, VA)

1991-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Novel alkylimidazolium/vanadium pentoxide intercalation compounds with excellent adsorption performance for methylene blue  

SciTech Connect

Novel alkylimidazolium-intercalated V{sub 2}O{sub 5} compounds were synthesized by a redox reaction between iodide ion and V{sub 2}O{sub 5}. The X-ray photoelectron spectroscopy and the diffuse reflectance UV-vis spectrometry experiments reveal that the vanadium in the intercalated V{sub 2}O{sub 5} products was partially reduced by an iodide ion and the resultant iodine can be removed in the final products. The transmission electron microscope observation and X-ray diffraction analysis testify that the prepared alkylimidazolium/V{sub 2}O{sub 5} intercalation compounds have typical lamellar structure with different d{sub 100} interlayer spacing values and the special straw-like nanofiber morphology with the length of 0.5-10 {mu}m. Systematic investigation indicates that new intercalation compounds possess the extraordinary adsorption performance for methylene blue in an aqueous solution. -- Graphical abstract: The alkylimidazolium-intercalated V{sub 2}O{sub 5} compounds with special straw-like nanofiber morphology were synthesized by a redox reaction between iodide ion and V{sub 2}O{sub 5}, which show the excellent adsorption performance for methylene blue in an aqueous medium. Display Omitted Research highlights: {yields} Novel alkylimidazolium-intercalated V{sub 2}O{sub 5} compounds. {yields} A simple preparation method by a redox reaction between iodide ion in ionic liquid and V{sub 2}O{sub 5}. {yields} The excellent adsorption performance for methylene blue in an aqueous medium.

Kong Aiguo; Ding Yongjie; Wang Ping; Zhang Hengqiang; Yang Fan [Department of Chemistry, East China Normal University, ShangHai City 200062 (China); Shan Yongkui, E-mail: ykshan@chem.ecnu.edu.c [Department of Chemistry, East China Normal University, ShangHai City 200062 (China)

2011-02-15T23:59:59.000Z

22

EA-1157: Methyl Chloride via Oxyhydrochlorination of Methane...  

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

1157: Methyl Chloride via Oxyhydrochlorination of Methane: A Building Black for Chemicals and Fuels from Natural Gas, Carrollton, Kentucky EA-1157: Methyl Chloride via...

23

Regenerable Hydrogen Chloride Removal Sorbent and Regenerable Multifunctional Hydrogen Sulfide and Hydrogen Chloride Removal Sorbent for High Temperature Gas Streams  

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

Hydrogen Chloride and Hydrogen Sulfide Hydrogen Chloride and Hydrogen Sulfide Removal Sorbents for High Temperature Gas Streams Opportunity The Department of Energy's National Energy Technology Laboratory (NETL) is seeking licensing partners interested in implementing United States Patent Number 7,767,000 entitled "Regenerable Hydrogen Chloride Removal Sorbent and Regenerable Multifunctional Hydrogen Sulfide and Hydrogen Chloride Removal Sorbent for High Temperature Gas Streams." Disclosed in this patent is the invention of a unique regenerable sorbent process that can remove contaminants from gas produced by the gasification of fossil fuels. Specifically, the process removes hydrogen chloride by using the regenerable sorbent and simultaneously extracts hydrogen chloride compounds and hydrogen

24

Absorption media for irreversibly gettering thionyl chloride  

DOE Patents (OSTI)

Thionyl chloride is a hazardous and reactive chemical used as the liquid cathode in commercial primary batteries. Contrary to previous thinking, ASZM-TEDA.RTM. carbon (Calgon Corporation) reversibly absorbs thionyl chloride. Thus, several candidate materials were examined as irreversible getters for thionyl chloride. The capacity, rate and effect of temperature were also explored. A wide variety of likely materials were investigated through screening experiments focusing on the degree of heat generated by the reaction as well as the material absorption capacity and irreversibility, in order to help narrow the group of possible getter choices. More thorough, quantitative measurements were performed on promising materials. The best performing getter was a mixture of ZnO and ASZM-TEDA.RTM. carbon. In this example, the ZnO reacts with thionyl chloride to form ZnCl.sub.2 and SO.sub.2. The SO.sub.2 is then irreversibly gettered by ASZM-TEDA.RTM. carbon. This combination of ZnO and carbon has a high capacity, is irreversible and functions effectively above -20.degree. C.

Buffleben, George (Tracy, CA); Goods, Steven H. (Livermore, CA); Shepodd, Timothy (Livermore, CA); Wheeler, David R. (Albuquerque, NM); Whinnery, Jr., LeRoy (Danville, CA)

2002-01-01T23:59:59.000Z

25

Viscosity and density tables of sodium chloride solutions  

DOE Green Energy (OSTI)

A file is presented containing tabulated data extracted from the scientific literature on the density and viscosity of aqueous sodium chloride solutions. Also included is a bibliography of the properties of aqueous sodium chloride solutions. (MHR)

Fair, J.A.; Ozbek, H. (comps.) [comps.

1977-04-01T23:59:59.000Z

26

Chloride-Exposed Steel-Reinforced Concrete Service Life ...  

Science Conference Proceedings (OSTI)

Chloride-Exposed Steel-Reinforced Concrete Service Life Prediction Program. Description/Summary: (Return to Cement ...

2013-06-11T23:59:59.000Z

27

Method for the regeneration of spent molten zinc chloride  

DOE Patents (OSTI)

In a process for regenerating spent molten zinc chloride which has been used in the hydrocracking of coal or ash-containing polynuclear aromatic hydrocarbonaceous materials derived therefrom and which contains zinc chloride, zinc oxide, zinc oxide complexes and ash-containing carbonaceous residue, by incinerating the spent molten zinc chloride to vaporize the zinc chloride for subsequent condensation to produce a purified molten zinc chloride: an improvement comprising the use of clay in the incineration zone to suppress the vaporization of metals other than zinc. Optionally water is used in conjunction with the clay to further suppress the vaporization of metals other than zinc.

Zielke, Clyde W. (McMurray, PA); Rosenhoover, William A. (Pittsburgh, PA)

1981-01-01T23:59:59.000Z

28

New SRMs  

Science Conference Proceedings (OSTI)

... SRM 1991 Mix Coal Tar/Petroleum Extract in Methylene Chloride ... NIST SRM 1991 Mixed Coal Tar/Petroleum Extract in Methylene Chloride ...

2013-07-30T23:59:59.000Z

29

New SRMs  

Science Conference Proceedings (OSTI)

... SRM 1991 Mix Coal Tar/Petroleum Extract in Methylene Chloride ... NIST SRM 1991 Mixed Coal Tar/Petroleum Extract in Methylene Chloride ...

2013-08-13T23:59:59.000Z

30

New and Renewal NIST SRMs/RMs  

Science Conference Proceedings (OSTI)

... SRM 1991 Mix Coal Tar/Petroleum Extract in Methylene Chloride ... NIST SRM 1991 Mixed Coal Tar/Petroleum Extract in Methylene Chloride ...

2013-07-01T23:59:59.000Z

31

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

32

Recovery of Precious Metals from Chloride Media Using Microalgae ...  

Science Conference Proceedings (OSTI)

Presentation Title, Recovery of Precious Metals from Chloride Media Using Microalgae Waste from Biofuel Extraction. Author(s), Katsutoshi Inoue, Kanjana ...

33

VOLATILE CHLORIDE PROCESS FOR THE RECOVERY OF METAL VALUES  

DOE Patents (OSTI)

A process is presented for recovering uranium, iron, and aluminum from centain shale type ores which contain uranium in minute quantities. The ore is heated wiih a chlorinating agent. such as chlorine, to form a volatilized stream of metal chlorides. The chloride stream is then passed through granular alumina which preferentially absorbs the volatile uranium chloride and from which the uranium may later be recovered. The remaining volatilized chlorides, chiefly those of iron and aluminum, are further treated to recover chlorine gas for recycle, and to recover ferric oxide and aluminum oxide as valuable by-products.

Hanley, W.R.

1959-01-01T23:59:59.000Z

34

EA-1157: Methyl Chloride via Oxyhydrochlorination of Methane: A Building  

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

57: Methyl Chloride via Oxyhydrochlorination of Methane: A 57: Methyl Chloride via Oxyhydrochlorination of Methane: A Building Black for Chemicals and Fuels from Natural Gas, Carrollton, Kentucky EA-1157: Methyl Chloride via Oxyhydrochlorination of Methane: A Building Black for Chemicals and Fuels from Natural Gas, Carrollton, Kentucky SUMMARY This EA evaluates the environmental impacts for the proposal to advance Oxyhydrochlorination technology to an integrated engineering-scale process. PUBLIC COMMENT OPPORTUNITIES None available at this time. DOCUMENTS AVAILABLE FOR DOWNLOAD September 27, 1996 EA-1157: Finding of No Significant Impact Methyl Chloride via Oxyhydrochlorination of Methane: A Building Black for Chemicals and Fuels from Natural Gas September 27, 1996 EA-1157: Final Environmental Assessment Methyl Chloride via Oxyhydrochlorination of Methane: A Building Black for

35

A method for synthesizing pollucite from chabazite and cesium chloride  

DOE Patents (OSTI)

A method is described for immobilizing waste chlorides salts containing radionuclides and hazardous nuclear material for permanent disposal, and in particular, a method for immobilizing waste chloride salts containing cesium, in a synthetic form of pollucite. The method for synthesizing pollucite from chabazite and cesium chloride includes mixing dry, non-aqueous cesium chloride with chabazite and heating the mixture to a temperature greater than the melting temperature of the cesium chloride, or above about 700 C. The method further comprises significantly improving the rate of retention of cesium in ceramic products comprised of a salt-loaded zeolite by adding about 10% chabazite by weight to the salt-loaded zeolite prior to conversion at elevated temperatures and pressures to the ceramic composite.

Pereira, Candido

1997-08-11T23:59:59.000Z

36

Method for synthesizing pollucite from chabazite and cesium chloride  

DOE Patents (OSTI)

A method is described for immobilizing waste chlorides salts containing radionuclides and hazardous nuclear material for permanent disposal, and in particular, a method is described for immobilizing waste chloride salts containing cesium, in a synthetic form of pollucite. The method for synthesizing pollucite from chabazite and cesium chloride includes mixing dry, non-aqueous cesium chloride with chabazite and heating the mixture to a temperature greater than the melting temperature of the cesium chloride, or above about 700 C. The method further comprises significantly improving the rate of retention of cesium in ceramic products comprised of a salt-loaded zeolite by adding about 10% chabazite by weight to the salt-loaded zeolite prior to conversion at elevated temperatures and pressures to the ceramic composite. 3 figs.

Pereira, C.

1999-02-23T23:59:59.000Z

37

CHLORIDE DEPOSITION FROM STEAM ONTO SUPERHEATER FUEL CLAD MATERIALS  

SciTech Connect

Experimemts using Cl/sup 36/ in a steam test loop were conducted to study the deposition behavior of chlorides on BONUS superheater fuel assembly materials. The moisture content of the steam was varied between 0 and 0.5 wt%, and superheat was added up to 15 deg F before the steam passed over the test cartridge heater. The effects of vaiiables on the chloride deposition on the heater were studied in detail. Chloride deposition from moist steam was found to result in heavy, adherent deposits which are conducive to severe chloride stress corrosion of austenitic steels, while removal of all moisture from the incoming steam reduces the chloride deposition and minimizes the chloride stress corrosion. The heater surface condition was found to be a very important variable; deposition is increased by surface defects and pits. Neither the temperature of steam or heater nor the amount of superheat had an appreciable effect on the deposition, when no moisture existed in the steam. However, low steam velocities and spacer protoberances increase the deposition. Different clad materials (Inconel and Type 304 and 347 stainless steel) with similar surface conditions did not affect the deposition, although subsequent corrosion effects do modify the deposition behavior. Recommendations are given for the control of chloride deposition in nuclear superheater reactor systems. (D.L.C.)

Bevilacqua, F.; Brown, G.M.

1963-10-18T23:59:59.000Z

38

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

39

Hydrogen chloride in superheated steam and chloride in deep brine at The Geysers geothermal field, California  

SciTech Connect

Chloride (Cl) concentrations of 10-120 ppm{sub w} have been measured in superheated steam produced by wells at The Geysers, a vapor-dominated geothermal field in northern California. Corrosion of the well casing and steam-gathering system has been recognized in some parts of The Geysers, and is apparently related to the presence of Cl. Cl in the steam is in a volatile form, generated with the steam at reservoir temperatures, and probably travels to the wellhead as HCl gas. Published experimental data for partial pressures of HCl in steam over aqueous HCl solutions and for dissociation constants of HCl were used to calculate distribution coefficients for HCl. Reservoir liquid Cl concentrations capable of generating steam with the observed Cl concentrations were then calculated as a function of pH and temperatures from 250 to 350º C. Equilibrium mineral/liquid reactions with the K-mica and K-feldspar assemblage found in the wells limit the reservoir liquid pH values at various Cl concentrations to about 5 to 6 (near neutral at 250 to 350º C). Within this pH range, liquid at 250º C could not produce steam containing the high Cl concentrations observed. However, liquid at higher temperatures (300 to 350º C) with chloride concentrations greater than 10,000 ppm{sub w} could generate steam with 10 to over 200 ppm{sub w} Cl. There is a positive correlation between pH and the chloride concentrations required to generate a given Cl concentration in steam. The concentration of Cl in superheated steam constrains not only the reservoir liquid composition, but the temperature at which the steam last equilibrated with liquid.

Haizlip, J.R.; Truesdell, A.H.

1988-01-01T23:59:59.000Z

40

Chloridizing Roasting-Smelting Reduction Methods Applied to ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Automatic electrochemical ambient air monitor for chloride and chlorine  

DOE Patents (OSTI)

An electrochemical monitoring system has been provided for determining chloride and chlorine in air at levels of from about 10-1000 parts per billion. The chloride is determined by oxidation to chlorine followed by reduction to chloride in a closed system. Chlorine is determined by direct reduction at a platinum electrode in 6 M H.sub.2 SO.sub.4 electrolyte. A fully automated system is utilized to (1) acquire and store a value corresponding to electrolyte-containing impurities, (2) subtract this value from that obtained in the presence of air, (3) generate coulometrically a standard sample of chlorine mixed with air sample, and determine it as chlorine and/or chloride, and (4) calculate, display, and store for permanent record the ratio of the signal obtained from the air sample and that obtained with the standard.

Mueller, Theodore R. (Oak Ridge, TN)

1976-07-13T23:59:59.000Z

42

Sources Of Chloride In Hydrothermal Fluids From The Valles Caldera...  

Open Energy Info (EERE)

Sources Of Chloride In Hydrothermal Fluids From The Valles Caldera, New Mexico- A 36Cl Study Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal Article:...

43

Reversibly Bound Chloride in the Atrial Natriuretic Peptide Receptor Hormone Binding Domain: Possible Allosteric Regulation and a Conserved Structural Motif for the Chloride-binding Site  

SciTech Connect

The binding of atrial natriuretic peptide (ANP) to its receptor requires chloride, and it is chloride concentration dependent. The extracellular domain (ECD) of the ANP receptor (ANPR) contains a chloride near the ANP-binding site, suggesting a possible regulatory role. The bound chloride, however, is completely buried in the polypeptide fold, and its functional role has remained unclear. Here, we have confirmed that chloride is necessary for ANP binding to the recombinant ECD or the full-length ANPR expressed in CHO cells. ECD without chloride (ECD(-)) did not bind ANP. Its binding activity was fully restored by bromide or chloride addition. A new X-ray structure of the bromide-bound ECD is essentially identical to that of the chloride-bound ECD. Furthermore, bromide atoms are localized at the same positions as chloride atoms both in the apo and in the ANP-bound structures, indicating exchangeable and reversible halide binding. Far-UV CD and thermal unfolding data show that ECD(-) largely retains the native structure. Sedimentation equilibrium in the absence of chloride shows that ECD(-) forms a strongly associated dimer, possibly preventing the structural rearrangement of the two monomers that is necessary for ANP binding. The primary and tertiary structures of the chloride-binding site in ANPR are highly conserved among receptor-guanylate cyclases and metabotropic glutamate receptors. The chloride-dependent ANP binding, reversible chloride binding, and the highly conserved chloride-binding site motif suggest a regulatory role for the receptor bound chloride. Chloride-dependent regulation of ANPR may operate in the kidney, modulating ANP-induced natriuresis.

Ogawa, H.; Qiu, Y; Philo, J; Arakawa, T; Ogata, C; Misono, K

2010-01-01T23:59:59.000Z

44

Repassivation Potential of Alloy 22 in Sodium and Calcium Chloride Brines  

SciTech Connect

A comprehensive matrix of 60 tests was designed to explore the effect of calcium chloride vs. sodium chloride and the ratio R of nitrate concentration over chloride concentration on the repassivation potential of Alloy 22. Tests were conducted using the cyclic potentiodynamic polarization (CPP) technique at 75 C and at 90 C. Results show that at a ratio R of 0.18 and higher nitrate was able to inhibit the crevice corrosion in Alloy 22 induced by chloride. Current results fail to show in a consistent way a different effect on the repassivation potential of Alloy 22 for calcium chloride solutions than for sodium chloride solutions.

Rebak, R B; Ilevbare, G O; Carranza, R M

2007-08-11T23:59:59.000Z

45

Two inorganic-organic hybrid materials based on polyoxometalate anions and methylene blue: Preparations, crystal structures and properties  

Science Conference Proceedings (OSTI)

Two novel inorganic-organic hybrid materials based on an organic dye cation methylene blue (MB) and Lindqvist-type POM polyanions, [C{sub 22}H{sub 18}N{sub 3}S]{sub 2}Mo{sub 6}O{sub 19} 2DMF (1) and [C{sub 22}H{sub 18}N{sub 3}S]{sub 2}W{sub 6}O{sub 19} 2DMF (2) were synthesized under ambient conditions and characterized by CV, IR spectroscopy, solid diffuse reflectance spectrum, UV-vis spectra in DMF solution, luminescent spectrum and single crystal X-ray diffraction. Crystallographic data reveal that compounds 1 and 2 are isostructural and both crystallize in the triclinic space group P1-bar . Their crystal structures present that the layers of organic molecules and inorganic anions array alternatively, and there exist strong {pi}...{pi} stacking interactions between dimeric MB cations and near distance interactions among organic dye cations, Lindqvist-type POM polyanions and DMF molecules. The solid diffuse reflectance spectra and UV-vis spectra in DMF solution appear new absorption bands ascribed to the charge-transfer transition between the cationic MB donor and the POM acceptors. Studies of the photoluminescent properties show that the formation of 1 and 2 lead to the fluorescence quenching of starting materials. -- Graphical abstract: Their crystal structures present that the layers of organic molecules and inorganic anions array alternatively, and there exist strong {pi}...{pi} stacking interactions between dimeric MB cations. Display Omitted

Nie Shanshan; Zhang Yaobin; Liu Bin; Li Zuoxi; Hu Huaiming [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, Department of Chemistry, Northwest University, Xi'an 710069 (China); Xue Ganglin, E-mail: xglin707@163.co [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, Department of Chemistry, Northwest University, Xi'an 710069 (China); Fu Feng; Wang Jiwu [Department of Chemistry, Yanan University, Yan'an 716000 (China)

2010-12-15T23:59:59.000Z

46

Lithium Diisopropylamide-Mediated Ortholithiations: Lithium Chloride Catalysis  

E-Print Network (OSTI)

Lithium Diisopropylamide-Mediated Ortholithiations: Lithium Chloride Catalysis Lekha Gupta, 2008 Ortholithiations of a range of arenes mediated by lithium diisopropylamide (LDA) in THF at -78 °C protocols with unpurified commercial samples of n-butyl- lithium to prepare LDA or commercially available

Collum, David B.

47

Oxidation of phosphine by iron(III) chloride complexes supported on activated charcoal  

SciTech Connect

It has been discovered that iron(III) chloride complexes supported on activated charcoal oxidize phosphine under normal conditions. The process accelerates as the concentration of the chloride ions and the proton acid increases.

Rakitskaya, T.L.; Kostyukova, I.S.; Red'ko, T.D.

1988-06-01T23:59:59.000Z

48

The ultra-high lime with aluminum process for removing chloride from recirculating cooling water  

E-Print Network (OSTI)

Chloride is a deleterious ionic species in cooling water systems because it is important in promoting corrosion. Chloride can be removed from cooling water by precipitation as calcium chloroaluminate using ultra-high lime with aluminum process (UHLA). The research program was conducted to study equilibrium characteristics and kinetics of chloride removal by UHLA process, study interactions between chloride and sulfate or silica, and develop a model for multicomponent removal by UHLA. Kinetics of chloride removal with UHLA was investigated. Chloride removal was found to be fast and therefore, removal kinetics should not be a limitation to applying the UHLA process. Equilibrium characteristics of chloride removal with UHLA were characterized. Good chloride removal was obtained at reasonable ranges of lime and aluminum doses. However, the stoichiometry of chloride removal with UHLA deviated from the theoretical stoichiometry of calcium chloroaluminate precipitation. Equilibrium modeling of experimental data and XRD analysis of precipitated solids indicated that this deviation was due to the formation of other solid phases such as tricalcium hydroxyaluminate and tetracalcium hydroxyaluminate. Effect of pH on chloride removal was characterized. Optimum pH for maximum chloride removal was pH 12 ± 0.2. Results of equilibrium experiments at different temperatures indicated that final chloride concentrations slightly increased when water temperature increased at temperatures below 40oC. However, at temperatures above 40oC, chloride concentration substantially increased with increasing water temperature. An equilibrium model was developed to describe chemical behavior of chloride removal from recycled cooling water using UHLA. Formation of a solid solution of calcium chloroaluminate, tricalcium hydroxyaluminate, and tetracalcium hydroxyaluminate was found to be the best mechanism to describe the chemical behavior of chloride removal with UHLA. Results of experiments that studied interactions between chloride and sulfate indicated that sulfate is preferentially removed over chloride. Final chloride concentration increased with increasing initial sulfate concentration. Silica was found to have only a small effect on chloride removal. The equilibrium model was modified in order to include sulfate and silica reactions along with chloride in UHLA process and it was able to accurately predict the chemical behavior of simultaneous removal of chloride, sulfate, and silica with UHLA.

Abdel-wahab, Ahmed Ibraheem Ali

2005-05-01T23:59:59.000Z

49

Why sequence ethene and vinyl chloride-oxidizing Mycobacterium strains?  

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

sequence ethene and vinyl sequence ethene and vinyl chloride-oxidizing Mycobacterium strains? Mycobacteria are known for causing human and animal diseases but they are also important degraders of hard-to-break-down water contaminants such as polyaromatic hydrocarbons (PAHs) and methyl tert-butyl ether (MTBE). So far the handful of bacterial species representing the Mycobacterium genus that have been sequenced all break down PAHs. In this project, researchers focus on the genomes of mycobacterial species isolated from soil, freshwater and marine environments that use the alkene compounds ethene and vinyl chloride as carbon sources. Chlorinated ethene compounds are difficult to remove from contaminated groundwater but necessary because of their toxicity. Additionally these compounds reduce the ozone levels in the atmosphere.

50

Thermophysical Properties of Sodium Nitrate and Sodium Chloride  

Office of Scientific and Technical Information (OSTI)

Thermophysical Properties of Sodium Nitrate and Sodium Chloride Thermophysical Properties of Sodium Nitrate and Sodium Chloride Solutions and Their Effects on Fluid Flow in Unsaturated Media Tianfu Xu and Karsten Pruess Earth Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 ABSTRACT. Understanding movement of saline sodium nitrate (NaNO 3 ) waste solutions is important for assessing the contaminant migration near leaking waste storage tanks in the unsaturated zone at the Hanford site (Washington, USA). The purpose of this study is to contribute a basic understanding of effects of the thermophysical behavior of NaNO 3 solutions on fluid flow in unsaturated media. We first present mathematical expressions for the dependence of density, viscosity, solubility and vapor pressure of

51

Mathematical Model of a Lithium/Thionyl Chloride Battery  

DOE Green Energy (OSTI)

A mathematical model of a spirally wound lithium/thionyl chloride primary battery has been developed ~d used for parameter estimation and design studies. The model formulation is based on the fimdarnental Consemation laws using porous electrode theory and concentrated solution theory. The model is used to estimate the difision coefficient and the kinetic parameters for the reactions at the anode and the cathode as a function of temperature. These parameters are obtained by fitting the simulated capacity and average cell voltage to experimental data over a wide range of temperatures (-55 to 49"C) and discharge loads (10 to 250 ohms). The experiments were performed on D-sized, cathode-limited, spirally wound lithium/thionyl chloride cells. The model is also used to study the effkct of cathode thickness on the cell capacity as a finction of temperature, and it was found that the optimum thickness for the cathode- limited design is temperature and load dependent.

Jain, M.; Jungst, R.G.; Nagasubramanian, G.; Weidner, J.W.

1998-11-24T23:59:59.000Z

52

Thionyl-chloride-induced lung injury and bronchiolitis obliterans  

SciTech Connect

Thionyl-chloride (TCl) is used in the manufacture of lithium batteries, producing SO2 and HCl fumes on contact with water. We report two cases of accidental TCl exposure resulting in lung injury that may vary from a relatively mild and reversible interstitial lung disease to a severe form of bronchiolitis obliterans causing, after a latent period, an acute/chronic respiratory failure as well as other complications (spontaneous pneumothorax and bronchopleural fistula), previously unreported in TCl fume inhalation.

Konichezky, S.; Schattner, A.; Ezri, T.; Bokenboim, P.; Geva, D. (Kaplan Hospital, Rehovot (Israel))

1993-09-01T23:59:59.000Z

53

Plutonium metal and alloy preparation by molten chloride reduction  

Science Conference Proceedings (OSTI)

Satisfactory reduction of molten plutonium trichloride (pure and in combination with 20 wt % sodium chloride) by calcium, lanthanum, and cerium has been demonstrated on the 10-g scale. The yields were satisfactory for this scale of operation, and it is indicated that these reductions may be useful for large-scale operations. Significant separations of plutonium from rare earth impurities was demonstrated for lanthanum and cerium reductions. Preparation of plutonium-cerium and plutonium-cerium-cobalt alloys during reduction was also demonstrated.

Reavis, J.G.

1984-01-01T23:59:59.000Z

54

Development of the Zinc-Chloride Battery for Utility Applications  

Science Conference Proceedings (OSTI)

This report reviews progress in Phase 2 (April 1978-March 1980) of a program to develop the zinc-chloride battery for utility load-leveling applications. Tasks in this phase included refurbishment of a 45-kWh module to increase capacity and efficiency, cycle testing of a 1.7-kWh battery, and development of a 50-kWh module to serve as the building block for the 4-MWh battery for the Battery Energy Test Facility.

1980-05-01T23:59:59.000Z

55

Uranium chloride 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 containing rare earth and noble metal fission products as well as other fission products is disclosed. The oxide fuel is reduced with Ca metal in the presence of Ca chloride and a U-Fe alloy which is liquid at about 800 C to dissolve uranium metal and the noble metal fission product metals and transuranium actinide metals and rare earth fission product metals leaving Ca chloride having CaO and fission products of alkali metals and the alkali earth metals and iodine dissolved therein. The Ca chloride and CaO and the fission products contained therein are separated from the U-Fe alloy and the metal values dissolved therein. The U-Fe alloy having dissolved therein reduced metals from the spent nuclear fuel is contacted with a mixture of one or more alkali metal or alkaline earth metal halides selected from the class consisting of alkali metal or alkaline earth metal and Fe or U halide or a combination thereof to transfer transuranium actinide metals and rare earth metals to the halide salt leaving the uranium and some noble metal fission products in the U-Fe alloy and thereafter separating the halide salt and the transuranium metals dissolved therein from the U-Fe alloy and the metals dissolved therein. 1 figure.

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

1992-08-25T23:59:59.000Z

56

Uranium chloride 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 containing rare earth and noble metal fission products as well as other fission products is disclosed. The oxide fuel is reduced with Ca metal in the presence of Ca chloride and a U-Fe alloy which is liquid at about 800.degree. C. to dissolve uranium metal and the noble metal fission product metals and transuranium actinide metals and rare earth fission product metals leaving Ca chloride having CaO and fission products of alkali metals and the alkali earth metals and iodine dissolved therein. The Ca chloride and CaO and the fission products contained therein are separated from the U-Fe alloy and the metal values dissolved therein. The U-Fe alloy having dissolved therein reduced metals from the spent nuclear fuel is contacted with a mixture of one or more alkali metal or alkaline earth metal halides selected from the class consisting of alkali metal or alkaline earth metal and Fe or U halide or a combination thereof to transfer transuranium actinide metals and rare earth metals to the halide salt leaving the uranium and some noble metal fission products in the U-Fe alloy and thereafter separating the halide salt and the transuranium metals dissolved therein from the U-Fe alloy and the metals dissolved therein.

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

1992-01-01T23:59:59.000Z

57

Uptake of chloride and carbonate ions by calcium monosulfoaluminate hydrate  

Science Conference Proceedings (OSTI)

Decommissioning of old nuclear reactors may produce waste streams containing chlorides and carbonates, including radioactive {sup 36}Cl{sup -} and {sup 14}CO{sub 3}{sup 2-}. Their insolubilization by calcium monosulfoaluminate hydrate was investigated. Carbonates were readily depleted from the solution, giving at thermodynamic equilibrium monocarboaluminate, monocarboaluminate + calcite, or calcite only, depending on the initial ratio between the anion and calcium monosulfoaluminate hydrate. Chloride ions reacted more slowly and were precipitated as Kuzel's salt, Kuzel's and Friedel's salts, or Friedel's salt only. Rietveld refinement of X-Ray powder diffraction patterns was successfully used to quantify the phase distributions, which were compared to thermodynamic calculations. Moreover, analysing the lattice parameters of Kuzel's salt as a function of its chloride content showed the occurrence of a restricted solid solution towards the sulfate side with general formula 3CaO{center_dot}Al{sub 2}O{sub 3}{center_dot}xCaCl{sub 2}{center_dot}(1 - x)CaSO{sub 4}{center_dot}(12 - 2x){center_dot}H{sub 2}O (0.36 {<=} x {<=} 0.50).

Mesbah, Adel [Commissariat a l'Energie Atomique et aux Energies Alternatives, CEA DEN/DTCD/SPDE, F-30207 Bagnols sur Ceze (France); Clermont Universite, ENSCCF, Laboratoire des Materiaux Inorganiques, BP 10448, F-63000 Clermont-Ferrand (France); Cau-dit-Coumes, Celine, E-mail: celine.cau-dit-coumes@cea.fr [Commissariat a l'Energie Atomique et aux Energies Alternatives, CEA DEN/DTCD/SPDE, F-30207 Bagnols sur Ceze (France); Renaudin, Guillaume [Clermont Universite, ENSCCF, Laboratoire des Materiaux Inorganiques, BP 10448, F-63000 Clermont-Ferrand (France); CNRS, UMR 6002, F-63177 Aubiere (France); Frizon, Fabien [Commissariat a l'Energie Atomique et aux Energies Alternatives, CEA DEN/DTCD/SPDE, F-30207 Bagnols sur Ceze (France); Leroux, Fabrice [Clermont Universite, Universite Blaise Pascal, Laboratoire des Materiaux Inorganiques, BP 10448, F-63000 Clermont-Ferrand (France); CNRS, UMR 6002, F-63177 Aubiere (France)

2012-08-15T23:59:59.000Z

58

Uranium chloride extraction of transuranium elements from LWR fuel  

Science Conference Proceedings (OSTI)

A process of separating transuranium actinide values from uranium values present in spent nuclear oxide fuels containing rare earth and noble metal fission products as well as other fission products is disclosed. The oxide fuel is reduced with Ca metal in the presence of Ca chloride and a U-Fe alloy which is liquid at about 800{degrees}C to dissolve uranium metal and the noble metal fission product metals and transuranium actinide metals and rare earth fission product metals leaving Ca chloride having CaO and fission products of alkali metals and the alkali earth metals and iodine dissolved therein. The Ca chloride and CaO and the fission products contained therein are separated from the U-Fe alloy and the metal values dissolved therein. The U-Fe alloy having dissolved therein reduced metals from the spent nuclear fuel is contacted with a mixture of one or more alkali metal or alkaline earth metal halides selected from the class consisting of alkali metal or alkaline earth metal and Fe or U halide or a combination thereof to transfer transuranium actinide metals and rare earth metals to the halide salt leaving the uranium and some noble metal fission products in the U-Fe alloy and thereafter separating the halide salt and the transuranium metals dissolved therein from the U-Fe alloy and the metals dissolved therein.

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

1991-12-31T23:59:59.000Z

59

Modeling acid-gas generation from boiling chloride brines  

Science Conference Proceedings (OSTI)

This study investigates the generation of HCl and other acid gases from boiling calcium chloride dominated waters at atmospheric pressure, primarily using numerical modeling. The main focus of this investigation relates to the long-term geologic disposal of nuclear waste at Yucca Mountain, Nevada, where pore waters around waste-emplacement tunnels are expected to undergo boiling and evaporative concentration as a result of the heat released by spent nuclear fuel. Processes that are modeled include boiling of highly concentrated solutions, gas transport, and gas condensation accompanied by the dissociation of acid gases, causing low-pH condensate. Simple calculations are first carried out to evaluate condensate pH as a function of HCl gas fugacity and condensed water fraction for a vapor equilibrated with saturated calcium chloride brine at 50-150 C and 1 bar. The distillation of a calcium-chloride-dominated brine is then simulated with a reactive transport model using a brine composition representative of partially evaporated calcium-rich pore waters at Yucca Mountain. Results show a significant increase in boiling temperature from evaporative concentration, as well as low pH in condensates, particularly for dynamic systems where partial condensation takes place, which result in enrichment of HCl in condensates. These results are in qualitative agreement with experimental data from other studies. The combination of reactive transport with multicomponent brine chemistry to study evaporation, boiling, and the potential for acid gas generation at the proposed Yucca Mountain repository is seen as an improvement relative to previously applied simpler batch evaporation models. This approach allows the evaluation of thermal, hydrological, and chemical (THC) processes in a coupled manner, and modeling of settings much more relevant to actual field conditions than the distillation experiment considered. The actual and modeled distillation experiments do not represent expected conditions in an emplacement drift, but nevertheless illustrate the potential for acid-gas generation at moderate temperatures (<150 C).

Zhang, Guoxiang; Spycher, Nicolas; Sonnenthal, Eric; Steefel, Carl

2009-11-16T23:59:59.000Z

60

Method of preparing sodalite from chloride salt occluded zeolite A  

DOE Patents (OSTI)

A method is described for immobilizing waste chloride salts containing radionuclides and hazardous nuclear material for permanent disposal starting with a substantially dry zeolite and sufficient glass to form leach resistance sodalite with occluded radionuclides and hazardous nuclear material. The zeolite and glass are heated to a temperature up to about 1,000 K to convert the zeolite to sodalite and thereafter maintained at a pressure and temperature sufficient to form a sodalite product near theoretical density. Pressure is used on the formed sodalite to produce the required density.

Lewis, M.A.; Pereira, C.

1995-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Method of preparing sodalite from chloride salt occluded zeolite  

DOE Patents (OSTI)

A method is described for immobilizing waste chloride salts containing radionuclides and hazardous nuclear material for permanent disposal starting with a substantially dry zeolite and sufficient glass to form leach resistant sodalite with occluded radionuclides and hazardous nuclear material. The zeolite and glass are heated to a temperature up to about 1000 K to convert the zeolite to sodalite and thereafter maintained at a pressure and temperature sufficient to form a sodalite product near theoretical density. Pressure is used on the formed sodalite to produce the required density.

Lewis, M.A.; Pereira, C.

1997-03-18T23:59:59.000Z

62

Development of a Novel High-Chloride Circuit for the Starfield ...  

Science Conference Proceedings (OSTI)

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

63

Influence of Chloride Content on Dielectric Behavior of C 3 A  

Science Conference Proceedings (OSTI)

Although this reaction has been widely studied, their electrical changes still require ... The results of the experimental work suggest that chloride ions modify the ...

64

Chloride-mass-balance for predicting increased recharge after land-use change  

E-Print Network (OSTI)

Key Words: precipitation, dry fallout, lysimeter, drainage,chloride input (from dry fallout and precipitation), andthan precipitation and fallout is likely the explanation for

Gee, G.W.; Zhang, Z.F.; Tyler, S.W.; Albright, W.H.; Singleton, M.J.

2004-01-01T23:59:59.000Z

65

The Dissolution Behavior of TiCxO1-x Solid Solutions in Chloride Melt  

Science Conference Proceedings (OSTI)

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

66

Synthesis of TiO2 by an Innovative Atmospheric Mixed Chloride ...  

Science Conference Proceedings (OSTI)

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

67

Optimizing Reinjection Strategy at Palinpinon, Philippines Based on Chloride Data  

DOE Green Energy (OSTI)

One of the guidelines established for the safe and efficient management of the Palinpinon Geothermal Field is to adopt a production and well utilization strategy such that the rapid rate and magnitude of reinjection fluid returns leading to premature thermal breakthrough would be minimized. To help achieve this goal, sodium fluorescein and radioactive tracer tests have been conducted to determine the rate and extent of communication between the reinjection and producing sectors of the field. The first objective of this paper is to show how the results of these tests, together with information on field geometry and operating conditions were used in algorithms developed in Operations Research to allocate production and reinjection rates among the different Palinpinon wells. Due to operational and economic constraints, such tracer tests were very limited in number and scope. This prevents obtaining information on the explicit interaction between each reinjection well and the producing wells. Hence, the chloride value of the producing well, was tested to determine if use of this parameter would enable identifying fast reinjection paths among different production/reinjection well pairs. The second aim, therefore, of this paper is to show the different methods of using the chloride data of the producing wells and the injection flow rates of the reinjection wells to provide a ranking of the pair of wells and, thereby, optimize the reinjection strategy of the field.

Urbino, Ma. Elena G.; Horne, Roland N.

1992-03-24T23:59:59.000Z

68

Optimizing reinjection strategy at Palinpinon, Philippines based on chloride data  

DOE Green Energy (OSTI)

One of the guidelines established for the safe and efficient management of the Palinpinon Geothermal Field is to adopt a production and well utilization strategy such that the rapid rate and magnitude of reinjection fluid returns leading to premature thermal breakthrough would be minimized. To help achieve this goal, sodium fluorescein and radioactive tracer tests have been conducted to determine the rate and extent of communication between the reinjection and producing sectors of the field. The first objective of this paper is to show how the results of these tests, together with information on field geometry and operating conditions were used in algorithms developed in Operations Research to allocate production and reinjection rates among the different Palinpinon wells. Due to operational and economic constraints, such tracer tests were very limited in number and scope. This prevents obtaining information on the explicit interaction between each reinjection well and the producing wells. Hence, the chloride value of the producing well, was tested to determine if use of this parameter would enable identifying fast reinjection paths among different production/reinjection well pairs. The second aim, therefore, of this paper is to show the different methods of using the chloride data of the producing wells and the injection flow rates of the reinjection wells to provide a ranking of the pair of wells and, thereby, optimize the reinjection strategy of the field.

Urbino, Ma. Elena G.; Horne, Roland N.

1991-01-01T23:59:59.000Z

69

High-temperature sodium nickel chloride battery for electric vehicles  

DOE Green Energy (OSTI)

Although the sodium-nickel chloride cell couple has a high voltage (2.59 V) and a high specific energy (790 Wh/kg), the performance of present incarnations of this battery tend to be limited by their power. Because the nickel chloride electrode dominates the resistance and weight of the cell, research on this cell couple at Argonne National Laboratory (ANL) has been primarily directed toward improving both the specific power and energy of the NiCl{sub 2} electrodes. During the course of these investigations a major breakthrough was achieved in lowering the impedance and increasing the usable capacity through the use of chemical additives and a tailored electrode morphology. This improved Ni/NiCl{sub 2} electrode has excellent performance characteristics, wide-temperature operation and fast recharge capability. Modeling studies done on this electrode indicate that a fully developed Na/NiCl{sub 2} battery based on ANL-single tube and bipolar designs would surpass the mid-term and approach the long-term goals of the US Advanced Battery Consortium.

Prakash, J.; Redey, L.; Nelson, P.A.; Vissers, D.R. [Argonne National Lab., IL (United States). Electrotechnical Technology Program

1996-07-01T23:59:59.000Z

70

Liquid Calcium Chloride Solar Storage: Concept and Analysis  

Science Conference Proceedings (OSTI)

Aqueous calcium chloride has a number of potential advantages as a compact and long-term solar storage medium compared to sensibly heated water. The combination of sensible and chemical binding energy of the liquid desiccant provides higher energy densities and lower thermal losses, as well as a temperature lift during discharge via an absorption heat pump. Calcium chloride is an excellent choice among desiccant materials because it is relatively inexpensive, non-toxic, and environmentally safe. This paper provides an overview of its application for solar storage and presents a novel concept for storing the liquid desiccant in a single storage vessel. The storage system uses an internal heat exchanger to add and discharge thermal energy and to help manage the mass, momentum, and energy transfer in the tank. The feasibility of the proposed concept is demonstrated via a computational fluid dynamic study of heat and mass transfer in the system over a range of Rayleigh, Lewis, Prandtl, and buoyancy ratio numbers expected in practice.

Quinnell, J. A.; Davidson, J. H.; Burch, J.

2010-01-01T23:59:59.000Z

71

Program on Technology Innovation: Chloride Attack-Induced Aging of Concrete Structures in the Energy Industry  

Science Conference Proceedings (OSTI)

Corrosion of embedded steel elements (reinforcement, liner, pre- or post-tensioning device) is a major cause of structure dysfunction resulting in large maintenance and repair costs worldwide. This report focuses on chloride attack–induced aging of concrete structures in the energy industry. Chloride attack is a common aging issue caused by marine environment, the extensive ...

2012-11-30T23:59:59.000Z

72

Sodium Chloride Hideout In a Simulated Steam Generator Tube and Tube Support Place Crevice  

Science Conference Proceedings (OSTI)

Localized corrosion of steam generator (SG) tubing in PWRs has been a serious problem that limits the life of this component. Preliminary measurements of sodium chloride hideout in simulated PWR SG crevices have shown that hideout rate increases with heat flux and concentration of sodium chloride in the bulk water.

1998-06-30T23:59:59.000Z

73

The Preparation and Property of Few-Layered Graphene/Benzalkonium Chloride Composite  

Science Conference Proceedings (OSTI)

In order to research and development a novel antibacterial material which is used to deal with the drinking water, few-layered grapheme/benzalkonium chloride composite was prepared by introducing different content of quaternary ammonium salt into layered ... Keywords: graphene, benzalkonium chloride, antibacterial, water treatment

A-gui Xie; Xiang Cai; Shao-zao Tan

2010-12-01T23:59:59.000Z

74

Self-discharge rate of lithium thionyl-chloride cells  

DOE Green Energy (OSTI)

Our low-rate lithium/thionyl-chloride ``D`` cell is required to provide power continuously for up to 10 years. The cell was designed at Sandia National Laboratories and manufactured at Eagle-Picher Industries, Joplin, Missouri. We have conducted accelerated aging studies at elevated temperatures to predict long-term performance of cells fabricated in 1992. Cells using 1.0M LiAlCl{sub 4} electrolyte follow Arrhenius kinetics with an activation energy of 14.6 Kcal/mol. This results in an annual capacity loss to self-discharge of 0.13 Ah at 25 C. Cells using a 1.0M LiAlCl{sub 4}{sm_bullet}SO{sub 2} electrolyte do not follow Arrhenius behavior. The performance of aged cells from an earlier fabrication lot is variable.

Cieslak, W.R.

1993-12-31T23:59:59.000Z

75

Development of mercury and chloride monitors for coal gasifiers  

DOE Green Energy (OSTI)

Ames Laboratory will develop an integrated sampling and analysis system suitable for on-line monitoring of mercury (Hg) and hydrogen chloride (HCl) in advanced coal-based gasifiers. The objectives of this project are to (1) summarize current technology for monitoring Hg and HCl in gaseous effluents; (2) identify analytical techniques for such determinations in high-temperature, high-pressure gases from coal-based systems for producing electrical power; (3) evaluate promising analytical approaches, and (4) produce reliable on-line monitors which are adaptable to plant-scale diagnostics and process control. For HG, the techniques selected for further consideration were atomic absorption and atomic fluorescence. For HCl, non-dispersive infrared absorption, a dry colorimetric procedure, and ion mobility spectroscopy were selected for testing in the laboratory. Results to date are described.

Buttermore, W.H.; Norton, G.A.; Chriswell, C.D.; Eckels, D.E.; Peters, R.E.

1996-12-31T23:59:59.000Z

76

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

77

TESTING OF 304L STAINLESS STEEL IN NITRIC ACID ENVIRONMENTS WITH FLUORIDES AND CHLORIDES  

Science Conference Proceedings (OSTI)

Impure radioactive material processed in nitric acid solutions resulted in the presence of chlorides in a dissolver fabricated from 304L stainless steel. An experimental program was conducted to study the effects of chloride in nitric acid/fluoride solutions on the corrosion of 304L stainless steel. The test variables included temperature (80, 95, and 110 C) and the concentrations of nitric acid (6, 12, and 14 M), fluoride (0.01, 0.1, and 0.2 M) and chloride (100, 350, 1000, and 2000 ppm). The impact of welding was also investigated. Results showed that the chloride concentration alone was not a dominant variable affecting the corrosion, but rather the interaction of chloride with fluoride significantly affected corrosion.

Mickalonis, J.

2010-10-04T23:59:59.000Z

78

Corrosive gas generation potential from chloride salt radiolysis in plutonium environments  

Science Conference Proceedings (OSTI)

The specific goal of this project was to evaluate the magnitude and practical significance of radiation effects involving mixtures of chloride salts and plutonium dioxide (PuO{sub 2}) sealed in stainless steel containers and stored for up to 50 yr, after stabilization at 950 C and packaging according to US Department of Energy (DOE) standards. The potential for generating chemically aggressive molecular chlorine (and hydrogen chloride by interaction with adsorbed water or hydrogen gas) by radiolysis of chloride ions was studied. To evaluate the risks, an annotated bibliography on chloride salt radiolysis was created with emphasis on effects of plutonium alpha radiation. The authors present data from the material identification and surveillance (MIS) project obtained from examination and analysis of representative PuO{sub 2} items from various DOE sites, including the headspace gas analysis data of sealed mixtures of PuO{sub 2} and chloride salts following long-term storage.

Tandon, L.; Allen, T.H.; Mason, R.E.; Penneman, R.A.

1999-07-01T23:59:59.000Z

79

Estimation of Groundwater Recharge at Pahute Mesa using the Chloride Mass-Balance Method  

SciTech Connect

Groundwater recharge on Pahute Mesa was estimated using the chloride mass-balance (CMB) method. This method relies on the conservative properties of chloride to trace its movement from the atmosphere as dry- and wet-deposition through the soil zone and ultimately to the saturated zone. Typically, the CMB method assumes no mixing of groundwater with different chloride concentrations; however, because groundwater is thought to flow into Pahute Mesa from valleys north of Pahute Mesa, groundwater flow rates (i.e., underflow) and chloride concentrations from Kawich Valley and Gold Flat were carefully considered. Precipitation was measured with bulk and tipping-bucket precipitation gauges installed for this study at six sites on Pahute Mesa. These data, along with historical precipitation amounts from gauges on Pahute Mesa and estimates from the PRISM model, were evaluated to estimate mean annual precipitation. Chloride deposition from the atmosphere was estimated by analyzing quarterly samples of wet- and dry-deposition for chloride in the bulk gauges and evaluating chloride wet-deposition amounts measured at other locations by the National Atmospheric Deposition Program. Mean chloride concentrations in groundwater were estimated using data from the UGTA Geochemistry Database, data from other reports, and data from samples collected from emplacement boreholes for this study. Calculations were conducted assuming both no underflow and underflow from Kawich Valley and Gold Flat. Model results estimate recharge to be 30 mm/yr with a standard deviation of 18 mm/yr on Pahute Mesa, for elevations >1800 m amsl. These estimates assume Pahute Mesa recharge mixes completely with underflow from Kawich Valley and Gold Flat. The model assumes that precipitation, chloride concentration in bulk deposition, underflow and its chloride concentration, have been constant over the length of time of recharge.

Cooper, Clay A [DRI] [DRI; Hershey, Ronald L [DRI] [DRI; Healey, John M [DRI] [DRI; Lyles, Brad F [DRI] [DRI

2013-07-01T23:59:59.000Z

80

Chloride removal from plutonium-aluminum alloy dissolver solution prior to purex solvent extraction  

Science Conference Proceedings (OSTI)

The Savannah River Plant (SRP), operated by E. I. du Pont de Nemours Co. for the United States Department of Energy, has successfully recovered plutonium from plutonium-aluminum alloy processed through the F-Canyon Separations facility. The alloy, produced at the Rocky Flats Plant, results from recovery of plutonium residues from spent chloride salts from pyrochemical processing. The alloy, termed scrub alloy'' or Rocky Flats scrub alloy'' (RFSA), contains up to 15 weight percent chloride impurity prior to mercuric ion catalyzed dissolution with fluoride-containing nitric acid. Solutions containing 850 to 3000 {mu}g/mL (parts per million) of chloride result. During subsequent Purex solvent extraction of this solution with 30% tri-n-butyl phosphate in normal paraffin diluent, chloride is rejected to the aqueous waste stream. This stream is eventually evaporated for waste treatment and acid recovery. Chloride concentrations in the product streams, subject to further processing, must be less than 100 {mu}g/mL to prevent excessive corrosion of equipment. This paper describes scrub alloy production at RFP, its dissolution and head end treatment to remove chloride, chloride values in subsequent processing streams including environmental discharges, and the turbidimetric analysis technique. 2 tabs.

Holcomb, H.P.

1990-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Probing Oxygen Activation Sites in Two Flavoprotein Oxidases Using Chloride as an Oxygen Surrogate  

SciTech Connect

A single basic residue above the si-face of the flavin ring is the site of oxygen activation in glucose oxidase (GOX) (His516) and monomeric sarcosine oxidase (MSOX) (Lys265). Crystal structures of both flavoenzymes exhibit a small pocket at the oxygen activation site that might provide a preorganized binding site for superoxide anion, an obligatory intermediate in the two-electron reduction of oxygen. Chloride binds at these polar oxygen activation sites, as judged by solution and structural studies. First, chloride forms spectrally detectable complexes with GOX and MSOX. The protonated form of His516 is required for tight binding of chloride to oxidized GOX and for rapid reaction of reduced GOX with oxygen. Formation of a binary MSOX-chloride complex requires Lys265 and is not observed with Lys265Met. Binding of chloride to MSOX does not affect the binding of a sarcosine analogue (MTA, methylthioactetate) above the re-face of the flavin ring. Definitive evidence is provided by crystal structures determined for a binary MSOX-chloride complex and a ternary MSOX-chloride-MTA complex. Chloride binds in the small pocket at a position otherwise occupied by a water molecule and forms hydrogen bonds to four ligands that are arranged in approximate tetrahedral geometry: Lys265:NZ, Arg49:NH1, and two water molecules, one of which is hydrogen bonded to FAD:N5. The results show that chloride (i) acts as an oxygen surrogate, (ii) is an effective probe of polar oxygen activation sites, and (iii) provides a valuable complementary tool to the xenon gas method that is used to map nonpolar oxygen-binding cavities.

Kommoju, Phaneeswara-Rao; Chen, Zhi-wei; Bruckner, Robert C.; Mathews, F. Scott; Jorns, Marilyn Schuman (Drexel-MED); (St. Louis-MED); (WU-MED)

2011-08-16T23:59:59.000Z

82

The faradaic efficiency of the lithium-thionyl chloride battery  

DOE Green Energy (OSTI)

The efficiency of converting chemical energy into electrical energy has been studied for the case of D-size, low and medium rate lithium-thionyl chloride (Li/TC) cells, under DC and various pulsed loads. Microcalorimetric monitoring of the heat output during discharge allowed the direct measurement of the faradaic efficiency, and showed that self-discharge is far more pervasive than previously acknowledged by researchers and battery manufacturers. Evaluations of the cell dynamics prove that current load and temperature fluctuations combine to disrupt the lithium passivation and to greatly enhance self-discharge. Typical faradaic efficiencies for DC range from abut 30% at low current density to 90% at moderate and 75% at high current density. Pulsed current further depresses these efficiency levels, except at very low average current densities. The decreased faradaic efficiency of Li/TC batteries in certain pulse situations needs to be studied further to define the range of applications for which it can be successfully used.

Hoier, S.N.; Eisenmann, E.T. [Sandia National Labs., Albuquerque, NM (United States). Battery Research Dept.

1996-04-01T23:59:59.000Z

83

FIRST DETECTION OF HYDROGEN CHLORIDE TOWARD PROTOSTELLAR SHOCKS  

Science Conference Proceedings (OSTI)

We present the first detection of hydrogen chloride in a protostellar shock by observing the fundamental transition at 626 GHz with the HIFI spectrometer. We detected two of the three hyperfine lines from which we derived a line opacity {15 K, and density >3 Multiplication-Sign 10{sup 5} cm{sup -3}. Combining these with the Herschel HIFI CO(5-4) observations allows us to further constrain the gas density and temperature, 10{sup 5}-10{sup 6} cm{sup -3} and 120-250 K, respectively, as well as the HCl column density, 2 Multiplication-Sign 10{sup 13} cm{sup -2}, and, finally, the abundance {approx}3-6 Multiplication-Sign 10{sup -9}. The estimated HCl abundance is consistent with that previously observed in low- and high-mass protostars. This puzzling result in the L1157-B1 shock, where species from volatile and refractory grain components are enhanced, suggests either that HCl is not the main reservoir of chlorine in the gas phase, which goes against previous chemical model predictions, or that the elemental chlorine abundance is low in L1157-B1. Astrochemical modeling suggests that HCl is in fact formed in the gas phase at low temperatures prior to the occurrence of the shock; the latter does not enhance its abundance.

Codella, C.; Vasta, M. [INAF, Osservatorio Astrofisico di Arcetri, Largo Enrico Fermi 5, I-50125 Firenze (Italy); Ceccarelli, C.; Lefloch, B.; Faure, A.; Wiesenfeld, L. [UJF-Grenoble 1/CNRS-INSU, Institut de Planetologie et d'Astrophysique de Grenoble (IPAG) UMR 5274, Grenoble, F-38041 (France); Bottinelli, S.; Caux, E. [Universite de Toulouse (France); UPS-OMP, CNRS, IRAP, Toulouse, BP 44346, F-31028 (France); Salez, M.; Cabrit, S. [Observatoire de Paris-Meudon, LERMA UMR CNRS 8112, Meudon (France); Viti, S., E-mail: codella@rcetri.astro.it [Department of Physics and Astronomy, University College London, London (United Kingdom)

2012-01-10T23:59:59.000Z

84

Sources Of Chloride In Hydrothermal Fluids From The Valles Caldera, New  

Open Energy Info (EERE)

Sources Of Chloride In Hydrothermal Fluids From The Valles Caldera, New Sources Of Chloride In Hydrothermal Fluids From The Valles Caldera, New Mexico- A 36Cl Study Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal Article: Sources Of Chloride In Hydrothermal Fluids From The Valles Caldera, New Mexico- A 36Cl Study Abstract The Valles caldera in New Mexico hosts a high-temperature geothermal system, which is manifested in a number of hot springs discharging in and around the caldera. In order to determine the fluid pathways and the origin of chloride in this system, we measured 36Cl/Cl ratios in waters from high-temperature drill holes and from surface springs in this region. The waters fall into two general categories: recent meteoric water samples with low Cl- concentrations (< 10 mg/L) and relatively high 36Cl/Cl ratios

85

Heat storage material comprising calcium chloride-hexahydrate and a nucleating agent  

SciTech Connect

The utility of calcium chloride-hexahydrate as a heat storage material is improved when barium carbonate, strontium carbonate, barium fluoride, barium fluoride-hydrofluoride and/or strontium fluoride is used as a nucleating agent to prevent supercooling.

Gawron, K.; Schroder, J.

1980-02-19T23:59:59.000Z

86

Nickel-Catalyzed Heck-Type Reactions of Benzyl Chlorides and Simple Olefins  

E-Print Network (OSTI)

Nickel-catalyzed intermolecular benzylation and heterobenzylation of unactivated alkenes to provide functionalized allylbenzene derivatives are described. A wide range of both the benzyl chloride and alkene coupling partners ...

Matsubara, Ryosuke

87

Contribution of garbage burning to chloride and PM[subscript 2.5] in Mexico City  

E-Print Network (OSTI)

The contribution of garbage burning (GB) emissions to chloride and PM[subscript 2.5] in the Mexico City Metropolitan Area (MCMA) has been investigated for the period of 24 to 29 March during the MILAGRO-2006 campaign using ...

Li, G.

88

Electrochemical Preparation of Ti2AlC in Molten Chloride Bath  

Science Conference Proceedings (OSTI)

Cathodic Behavior of Silicon (?) in BaF2-CaF2 –SiO2 Melts ... Electrochemical Impedance Spectroscopy of Uranium Chloride in Molten LiCl-KCl Eutectic.

89

Iron (III) Chloride doping of large-area chemical vapor deposition graphene  

E-Print Network (OSTI)

Chemical doping is an effective method of reducing the sheet resistance of graphene. This thesis aims to develop an effective method of doping large area Chemical Vapor Deposition (CVD) graphene using Iron (III) Chloride ...

Song, Yi, S.M. Massachusetts Institute of Technology

2013-01-01T23:59:59.000Z

90

Method for immobilizing mixed waste chloride salts containing radionuclides and other hazardous wastes  

DOE Patents (OSTI)

The invention is a method for the encapsulation of soluble radioactive waste chloride salts containing radionuclides such as strontium, cesium and hazardous wastes such as barium so that they may be permanently stored without future threat to the environment. The process consists of contacting the salts containing the radionuclides and hazardous wastes with certain zeolites which have been found to ion exchange with the radionuclides and to occlude the chloride salts so that the resulting product is leach resistant.

Lewis, Michele A. (Naperville, IL); Johnson, Terry R. (Wheaton, IL)

1993-01-01T23:59:59.000Z

91

Raman spectroscopic studies of chemical speciation in calcium chloride melts  

DOE Green Energy (OSTI)

Raman spectroscopy was applied to CaCl2 melts at 900 degrees C under both non-electrolyzed and electrolyzed conditions. The later used titania cathodes supplied by TIMET, Inc. and graphite anodes. Use of pulse-gating to collect the Raman spectra successfully eliminated any interference from black-body radiation and other stray light. The spectrum of molten CaCl2 exhibited no distinct, resolvable bands that could be correlated with a calcium chloride complex similar to MgCl42- in MgCl2 melts. Rather, the low frequency region of the spectrum was dominated by a broad “tail” arising from collective oscillations of both charge and mass in the molten salt “network.” Additions of both CaO and Ca at concentrations of a percent or two resulted in no new features in the spectra. Addition of CO2, both chemically and via electrolysis at concentrations dictated by stability and solubility at 900 degrees C and 1 bar pressure, also produced no new bands that could be correlated with either dissolved CO2 or the carbonate ion. These results indicated that Raman spectroscopy, at least under the conditions evaluated in the research, was not well suited for following the reactions and coordination chemistry of calcium ions, nor species such as dissolved metallic Ca and CO2 that are suspected to impact current efficiency in titanium electrolysis cells using molten CaCl2. Raman spectra of TIMET titania electrodes were successfully obtained as a function of temperature up to 900 degrees C, both in air and in-situ in CaCl2 melts. However, spectra of these electrodes could only be obtained when the material was in the unreduced state. When reduced, either with hydrogen or within an electrolysis cell, the resulting electrodes exhibited no measurable Raman bands under the conditions used in this work.

Windisch, Charles F.; Lavender, Curt A.

2005-02-01T23:59:59.000Z

92

Lithium: Thionyl chloride battery state-of-the-art assessment  

DOE Green Energy (OSTI)

Models of the performance of primary Li/SOCl{sub 2} cells can provide for realistic comparisons between technical information from different sources, and set standards that electronic circuit designers may refer to in the generation of high-quality products. Data from various investigators were used to derive mathematical- statistical relationships with physical design features (e.g. size and materials), operating parameters (e.g. current and temperature) and storage conditions (time and temperature). These efforts were substantially promoted by normalization procedures. For example, current loads were converted into current densities, or if appropriate, into current per unit cathode volume. Similarly, cell capacities were standardized with the maximum values observed at low current and also with respect to the cathode volume. Particular emphasis was placed on evaluations of voltage-delay, cell capacity and self-discharge, for which several equations were established. In spite of a considerable expenditure in time to find high-quality datasets, the reality is that all of the reviewed studies are flawed in one way or another. Specifically, all datasets are afflicted with sizable experimental errors and the precision of the regression equations is much lower than is deemed necessary for a universal model of the lithium thionyl chloride cell. Each of the equations has some definite truth content, but is generally incapable of bridging the gap between different studies. The basic failure to come up with a unifying model for Li/SOCl{sub 2} batteries leaves only one benefit of the present analysis, namely to provide guidance for future investigations. Several recommendations are made based on the insight gained during the search for good data in the relevant literature.

Eisenmann, E.T.

1996-03-01T23:59:59.000Z

93

Effect of chloride content of molten nitrate salt on corrosion of A516 carbon steel.  

SciTech Connect

The corrosion behavior of A516 carbon steel was evaluated to determine the effect of the dissolved chloride content in molten binary Solar Salt. Corrosion tests were conducted in a molten salt consisting of a 60-40 weight ratio of NaNO{sub 3} and KNO{sub 3} at 400{sup o}C and 450{sup o}C for up to 800 hours. Chloride concentrations of 0, 0.5 and 1.0 wt.% were investigated to determine the effect on corrosion of this impurity, which can be present in comparable amounts in commercial grades of the constituent salts. Corrosion rates were determined by descaled weight losses, corrosion morphology was examined by metallographic sectioning, and the types of corrosion products were determined by x-ray diffraction. Corrosion proceeded by uniform surface scaling and no pitting or intergranular corrosion was observed. Corrosion rates increased significantly as the concentration of dissolved chloride in the molten salt increased. The adherence of surface scales, and thus their protective properties, was degraded by dissolved chloride, fostering more rapid corrosion. Magnetite was the only corrosion product formed on the carbon steel specimens, regardless of chloride content or temperature.

Bradshaw, Robert W.; Clift, W. Miles

2010-11-01T23:59:59.000Z

94

DOEEA-1157 ENVIRONlMENTAL ASSESSMENT METHYL CHLORIDE VIA OXYHYDROCHLOFUNATION OF METHANE:  

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

57 57 ENVIRONlMENTAL ASSESSMENT METHYL CHLORIDE VIA OXYHYDROCHLOFUNATION OF METHANE: A BUILDING BLOCK FOR CHEMICALS AND FUELS FROM NATURAL GAS DOW CORNING CORPORATION CARROLLTON, KENTUCKY SEPTEMBER 1996 U.S. DEPARTMENT OF ENERGY PITTSBURGH ENERGY TECHNOLOGY CENTER CUM ~~~~~~~~ DOEEA-1157 ENVIRONlMENTAL ASSESSMENT METHYL CHLORIDE VIA OXYHYDROCHLORINATION OF METHANE: A BUILDING BLOCK FOR CHEMICALS AND FUELS FROM NATURAL GAS DOW CORNING CORPORATION CARROLLTON, KENTUCKY SEPTEMBER 1996 U.S. DEPARTMENT OF ENERGY PITTSBURGH ENERGY TECHNOLOGY CENTER Portions of this document may be illegible in electronic image products. Image are produced from the best available original document. &E/,Etq --,/s7 FINDING OF NO SIGNIFICANT IMPACT FOR THE PROPOSED METHYL CHLORIDE V

95

Current techniques in acid-chloride corrosion control and monitoring at The Geysers  

DOE Green Energy (OSTI)

Acid chloride corrosion of geothermal well casings, production piping and power plant equipment has resulted in costly corrosion damage, frequent curtailments of power plants and the permanent shut-in of wells in certain areas of The Geysers. Techniques have been developed to mitigate these corrosion problems, allowing continued production of steam from high chloride wells with minimal impact on production and power generation facilities.The optimization of water and caustic steam scrubbing, steam/liquid separation and process fluid chemistry has led to effective and reliable corrosion mitigation systems currently in routine use at The Geysers. When properly operated, these systems can yield steam purities equal to or greater than those encountered in areas of The Geysers where chloride corrosion is not a problem. Developments in corrosion monitoring techniques, steam sampling and analytical methodologies for trace impurities, and computer modeling of the fluid chemistry has been instrumental in the success of this technology.

Hirtz, Paul; Buck, Cliff; Kunzman, Russell

1991-01-01T23:59:59.000Z

96

LOW TEMPERATURE PROCESS FOR THE REMOVAL AND RECOVERY OF CHLORIDES AND NITRATES FROM AQUEOUS NITRATE SOLUTIONS  

DOE Patents (OSTI)

A method is described for reducing the chloride content of a solution derived from the dissolution of a stainless steel clad nuclear fuel element with an aqua regia dissolution medium. The solutlon is adjusted to a nitric acid concentration in the range 5 to 10 M and is countercurrently contacted at room temperature with a gaseous oxide of nitrogen selected from NO, NO/sub 2/, N/sub 2/ O/sub 3/, and N/sub 2/O/sub 4/. Chlo ride is recovered from the contacted solution as nitrosyl chloride. After reduction of the chloride content, the solution is then contacted with gaseous NO to reduce the nitric acid molarity to a desired level. (AEC)

Savolainen, J.E.

1963-01-29T23:59:59.000Z

97

Method for determining trace quantities of chloride in polymeric materials using ion selective electrodes: Final report  

Science Conference Proceedings (OSTI)

A method for determining trace quantities of chloride in polymeric materials has been developed. Ion-selective electrodes and the standard addition method were used in all the analyses. The ion-selective electrode method was compared with neutron activation, ion chromatography and chloridometer titration. The ion-selective electrode technique results for chloride were similar to those of neutron activation, which is the acknowledged referee method. This ion-selective electrode method showed the highest standard recovery when compared with the ion chromatography and chloridometer titration methods.

Salary, J.

1987-02-01T23:59:59.000Z

98

Method of electrode fabrication and an electrode for metal chloride battery  

DOE Patents (OSTI)

A method of fabricating an electrode for use in a metal chloride battery and an electrode are provided. The electrode has relatively larger and more uniform pores than those found in typical electrodes. The fabrication method includes the steps of mixing sodium chloride particles selected from a predetermined size range with metal particles selected from a predetermined size range, and then rigidifying the mixture. The electrode exhibits lower resistivity values of approximately 0.5 [Omega]cm[sup 2] than those resistivity values of approximately 1.0-1.5 [Omega]cm[sup 2] exhibited by currently available electrodes.

Bloom, I.D.; Nelson, P.A.; Vissers, D.R.

1993-03-16T23:59:59.000Z

99

Method of electrode fabrication and an electrode for metal chloride battery  

DOE Patents (OSTI)

A method of fabricating an electrode for use in a metal chloride battery and an electrode are provided. The electrode has relatively larger and more uniform pores than those found in typical electrodes. The fabrication method includes the steps of mixing sodium chloride particles selected from a predetermined size range with metal particles selected from a predetermined size range, and then rigidifying the mixture. The electrode exhibits lower resistivity values of approximately 0.5 {Omega}cm{sup 2} than those resistivity values of approximately 1.0--1.5 {Omega}cm{sup 2} exhibited by currently available electrodes.

Bloom, I.D.; Nelson, P.A.; Vissers, D.R.

1990-10-09T23:59:59.000Z

100

Method of electrode fabrication and an electrode for metal chloride battery  

SciTech Connect

A method of fabricating an electrode for use in a metal chloride battery and an electrode are provided. The electrode has relatively larger and more uniform pores than those found in typical electrodes. The fabrication method includes the steps of mixing sodium chloride particles selected from a predetermined size range with metal particles selected from a predetermined size range, and then rigidifying the mixture. The electrode exhibits lower resistivity values of approximately 0.5 .OMEGA.cm.sup.2 than those resistivity values of approximately 1.0-1.5 .OMEGA.cm.sup.2 exhibited by currently available electrodes.

Bloom, Ira D. (Bolingbrook, IL); Nelson, Paul A. (Wheaton, IL); Vissers, Donald R. (Naperville, IL)

1993-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Current Status of Health and Safety Issues of Sodium/Metal Chloride (Zebra) Batteries  

DOE Green Energy (OSTI)

This report addresses environmental, health, and safety (EH&S) issues associated with sodium/ metal chloride batteries, in general, although most references to specific cell or battery types refer to units developed or being developed under the Zebra trademark. The report focuses on issues pertinent to sodium/metal chloride batteries and their constituent components; however, the fact that some ''issues'' arise from interaction between electric vehicle (EV) and battery design compels occasional discussion amid the context of EV vehicle design and operation. This approach has been chosen to provide a reasonably comprehensive account of the topic from a cell technology perspective and an applications perspective.

Trickett, D.

1998-12-15T23:59:59.000Z

102

Reliability, Availability, and Maintainability Assessment of a Zinc Chloride Battery System  

Science Conference Proceedings (OSTI)

UNIRAM analyses guided the design of an advanced energy storage system for load leveling and management. The study showed that, in comparison with competing technologies that are available approximately 90% of the time, a 2-MW system of zinc chloride batteries would have an availability greater than 98%.

1986-12-10T23:59:59.000Z

103

Low coverage spontaneous etching and hyperthermal desorption of aluminum chlorides from Cl2 Al,,111...  

E-Print Network (OSTI)

spectrometry has been used to monitor the desorption of aluminum chloride (AlxCly) etch products from the Al-probable velocity of 517 22 m/s at an Al 111 surface temperature of 100 K. This corresponds to 22 times the expected thermal desorption translational energy for AlCl3 . Cl2 sticking probability measurements and AlxCly etch

Kummel, Andrew C.

104

Lithium chloride protects retinal neurocytes from nutrient deprivation by promoting DNA non-homologous end-joining  

SciTech Connect

Lithium chloride is a therapeutic agent for treatment of bipolar affective disorders. Increasing numbers of studies have indicated that lithium has neuroprotective effects. However, the molecular mechanisms underlying the actions of lithium have not been fully elucidated. This study aimed to investigate whether lithium chloride produces neuroprotective function by improving DNA repair pathway in retinal neurocyte. In vitro, the primary cultured retinal neurocytes (85.7% are MAP-2 positive cells) were treated with lithium chloride, then cultured with serum-free media to simulate the nutrient deprived state resulting from ischemic insult. The neurite outgrowth of the cultured cells increased significantly in a dose-dependent manner when exposed to different levels of lithium chloride. Genomic DNA electrophoresis demonstrated greater DNA integrity of retinal neurocytes when treated with lithium chloride as compared to the control. Moreover, mRNA and protein levels of Ligase IV (involved in DNA non-homologous end-joining (NHEJ) pathway) in retinal neurocytes increased with lithium chloride. The end joining activity assay was performed to determine the role of lithium on NHEJ in the presence of extract from retinal neurocytes. The rejoining levels in retinal neurocytes treated with lithium were significantly increased as compared to the control. Furthermore, XRCC4, the Ligase IV partner, and the transcriptional factor, CREB and CTCF, were up-regulated in retinal cells after treating with 1.0 mM lithium chloride. Therefore, our data suggest that lithium chloride protects the retinal neural cells from nutrient deprivation in vitro, which may be similar to the mechanism of cell death in glaucoma. The improvement in DNA repair pathway involving in Ligase IV might have an important role in lithium neuroprotection. This study provides new insights into the neural protective mechanisms of lithium chloride.

Zhuang Jing; Li Fan; Liu Xuan; Liu Zhiping; Lin Jianxian [State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, 54 S Xianlie Road, Guangzhou, Guangdong 510060 (China); Ge Yihong [Department of Stomatology, the Southern Medical University (China); Kaminski, Joseph M. [National Institute of Allergy and Infectious Diseases, Division of Allergy, Immunology, and Transplantation, University of South Alabama (United States); Summers, James Bradley [Department of Radiology, University of South Alabama (United States); Wang Zhichong [State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, 54 S Xianlie Road, Guangzhou, Guangdong 510060 (China); Ge Jian [State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, 54 S Xianlie Road, Guangzhou, Guangdong 510060 (China)], E-mail: gejian@mail.sysu.edu.cn; Yu Keming [State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, 54 S Xianlie Road, Guangzhou, Guangdong 510060 (China)], E-mail: yukeming@mail.sysu.edu.cn

2009-03-13T23:59:59.000Z

105

LOCALIZED CORROSION OF AUSTENITIC STAINLESS STEELEXPOSED TO MIXTURES OF PLUTONIUM OXIDE AND CHLORIDE SALTS  

SciTech Connect

Laboratory corrosion tests were conducted to investigate the corrosivity of moist plutonium oxide/chloride (PuO{sub 2}/Cl-) salt mixtures on 304L and 316L stainless steel coupons. The tests exposed flat coupons for pitting evaluation and 'teardrop' stressed coupons for stress corrosion cracking (SCC) evaluation at room temperature to various mixtures of PuO{sub 2} and chloride-bearing salts for periods up to 500 days. The two flat coupons were placed so that the solid oxide/salt mixture contacted about one half of the coupon surface. One teardrop coupon was placed in contact with solid mixture; the second teardrop was in contact with the headspace gas only. The mixtures were loaded with nominally 0.5 wt % water under a helium atmosphere. Observations of corrosion ranged from superficial staining to pitting and SCC. The extent of corrosion depended on the total salt concentration and on the composition of the salt. The most significant corrosion was found in coupons that were exposed to 98 wt % PuO{sub 2}, 2 wt % chloride salt mixtures that contained calcium chloride. SCC was observed in two 304L stainless steel teardrop coupons exposed in solid contact to a mixture of 98 wt % PuO{sub 2}, 0.9 wt % NaCl, 0.9 wt % KCl, and 0.2 wt % CaCl{sub 2}. The cracking was associated with the heat-affected zone of an autogenous weld that ran across the center of the coupon. Cracking was not observed in coupons exposed to the headspace gas, nor in coupons exposed to other mixtures with either 0.92 wt% CaCl{sub 2} or no CaCl{sub 2}. The corrosion results point to the significance of the interaction between water loading and the concentration of the hydrating salt CaCl{sub 2} in the susceptibility of austenitic stainless steels to corrosion.

Zapp, P; Kerry Dunn, K; Jonathan Duffey, J; Ron Livingston, R; Zane Nelson, Z

2008-11-21T23:59:59.000Z

106

Reaction of uranium oxides with chlorine and carbon or carbon monoxide to prepare uranium chlorides  

SciTech Connect

The preferred preparation concept of uranium metal for feed to an AVLIS uranium enrichment process requires preparation of uranium tetrachloride (UCI{sub 4}) by reacting uranium oxides (UO{sub 2}/UO{sub 3}) and chlorine (Cl{sub 2}) in a molten chloride salt medium. UO{sub 2} is a very stable metal oxide; thus, the chemical conversion requires both a chlorinating agent and a reducing agent that gives an oxide product which is much more stable than the corresponding chloride. Experimental studies in a quartz reactor of 4-cm ID have demonstrated the practically of some chemical flow sheets. Experimentation has illustrated a sequence of results concerning the chemical flow sheets. Tests with a graphite block at 850{degrees}C demonstrated rapid reactions of Cl{sub 2} and evolution of carbon dioxide (CO{sub 2}) as a product. Use of carbon monoxide (CO) as the reducing agent also gave rapid reactions of Cl{sub 2} and formation of CO{sub 2} at lower temperatures, but the reduction reactions were slower than the chlorinations. Carbon powder in the molten salt melt gave higher rates of reduction and better steady state utilization of Cl{sub 2}. Addition of UO{sub 2} feed while chlorination was in progress greatly improved the operation by avoiding the plugging effects from high UO{sub 2} concentrations and the poor Cl{sub 2} utilizations from low UO{sub 2} concentrations. An UO{sub 3} feed gave undesirable effects while a feed of UO{sub 2}-C spheres was excellent. The UO{sub 2}-C spheres also gave good rates of reaction as a fixed bed without any molten chloride salt. Results with a larger reactor and a bottom condenser for volatilized uranium show collection of condensed uranium chlorides as a loose powder and chlorine utilizations of 95--98% at high feed rates. 14 refs., 7 figs., 14 tabs.

Haas, P.A.; Lee, D.D.; Mailen, J.C.

1991-11-01T23:59:59.000Z

107

THE PREPARATION OF URANIUM DIOXIDE FROM A MOLTEN SALT SOLUTION OF URANYL CHLORIDE  

DOE Green Energy (OSTI)

Uranium oxides in a molten eutectic mixture of NaClKCl were chlorinated by bubbling chlorine gas through the mixture. The reaction product, uranyl chloride. was soluble in the molten salt. Although UO/sub 2/ was the most common oxide used, the reaction was similar in the other oxides. Phosgene and aluminum chloride were also used as chlorinating agents. A dense, crystalline precipitate of pure UO/sub 2/ was prepared by the reduction of the uranyl chloride contained in the molten salt solution. The reduction was accomplished by contacting the salt solution with any of several metals, by reaction with hydrogen or dry ammonia gas, or by electrolysis. Several kilograms of UO/sub 2/ were prepared by electrolysis using graphite electrodes. The physical properties of the material made it potentially useful as a ceramic fuel material. The initial high particle density of the "as-produced" UO/sub 2/ was considered of great potential advantage for adapting this process to the refabrication of irradiated UO/sub 2/ into recycle fuel elements. (M.C.G.)

Lyon, W.L.; Voiland, E.E.

1959-10-20T23:59:59.000Z

108

The Effects of Temperature on the Electrochemical Performance of Sodium-Nickel Chloride Batteries  

Science Conference Proceedings (OSTI)

The sodium-nickel chloride (ZEBRA) battery is typically fabricated with a thick tubular ?"-alumina solid electrolyte (BASE) and operated at relatively high temperatures (? 300ºC) to achieve adequate electrochemical performance. In the present work, a planar-type sodium-nickel chloride battery possessing a thin BASE (~600 ?m thick) was tested in order to evaluate the feasibility of the battery operation at low temperatures (?200°C). Electrochemical test results revealed that the battery was able to be cycled at C/3 rate at as low as 175°C despite the higher cell polarization at the reduced temperature. Overall, low operating temperature resulted in a considerable improvement in the stability of cell performance. Cell degradation was negligible at 175°C, while 55% increase in end-of-charge polarization was observed at 280°C after 60 cycles. SEM analysis indicated that the performance degradation at higher temperatures was related to the particle growth of both nickel and sodium chloride in the cathode. The cells tested at lower temperatures (e.g., 175 and 200°C), however, exhibited a sharp drop in cell voltage at the end of discharge due to the diffusion limitation, possibly caused by the limited ionic conductivity of NaAlCl4 melt or the poor wettability of sodium on the BASE. Therefore, improvements in the ionic conductivity of a secondary electrolyte and sodium wetting are desirable to further enhance the battery performance at low temperatures.

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

2012-10-01T23:59:59.000Z

109

Experimental and theoretical investigation of the production of HCl and some metal chlorides in magmatic/hydrothermal systems. Progress report  

DOE Green Energy (OSTI)

Hydrothermal experiments on the partitioning of HCl and copper chloride in the system silicate melt-hydrosaline liquid-aqueous vapor are described. Modelling of the aqueous phase evolution process is discussed. (MHR)

Not Available

1990-12-31T23:59:59.000Z

110

Optimal estimation of the surface fluxes of methyl chloride using a 3-D global chemical transport model  

E-Print Network (OSTI)

Methyl chloride (CH3Cl) [CH subscript 3 Cl] is a chlorine-containing trace gas in the atmosphere contributing significantly to stratospheric ozone depletion. Large uncertainties in estimates of its source and sink magnitudes ...

Xiao, Xue

111

Nickel-catalyzed asymmetric cross-couplings of secondary allylic chlorides and planar-chiral compounds in asymmetric synthesis  

E-Print Network (OSTI)

In Part I, nickel-catalyzed asymmetric carbon-carbon bond-forming reactions are described. A nickel/Pybox system effectively catalyzes regio- and enantioselective cross-couplings between racemic secondary allylic chlorides ...

Son, Sunghee

2008-01-01T23:59:59.000Z

112

EFFECT OF CHLORIDE AND SULFATE CONCENTRATION ON PROBABLITY BASED CORROSION CONTROL FOR LIQUID WASTE TANKS- PART IV  

SciTech Connect

A series of cyclic potentiodynamic polarization tests was performed on samples of A537 carbon steel in support of a probability-based approach to evaluate the effect of chloride and sulfate on corrosion susceptibility. Testing solutions were chosen to build off previous experimental results from FY07, FY08, FY09 and FY10 to systemically evaluate the influence of the secondary aggressive species, chloride, and sulfate. The FY11 results suggest that evaluating the combined effect of all aggressive species, nitrate, chloride, and sulfate, provides a consistent response for determining corrosion susceptibility. The results of this work emphasize the importance for not only nitrate concentration limits, but also chloride and sulfate concentration limits as well.

Hoffman, E.

2012-08-23T23:59:59.000Z

113

A Basic Study on Development of a Swell-Peeling Method in UBC ...  

Science Conference Proceedings (OSTI)

Aug 1, 2000... them using a methylene chloride solution with acids and it works very well. ... by the coexisting acid, especially halogenated acetic acid.

114

Generalized chloride mass balance: Forward and inverse solutions for one-dimensional tracer convection under transient flux  

Science Conference Proceedings (OSTI)

Forward and inverse solutions are provided for analysis of inert tracer profiles resulting from one-dimensional convective transport under fluxes which vary with time and space separately. The developments are displayed as an extension of conventional chloride mass balance (CMB) techniques to account for transient as well as space-dependent water fluxes. The conventional chloride mass balance has been used over two decades to estimate recharge over large time scales in arid environments. In this mass balance approach, the chloride concentration in the pore water, originating from atmospheric fallout, is inversely proportional to the flux of water through the sediments. The CMB method is especially applicable to arid and semi-arid regions where evapotranspirative enrichment of the pore water produces a distinct chloride profile in the unsaturated zone. The solutions presented allow incorporation of transient fluxes and boundary conditions in CMB analysis, and allow analysis of tracer profile data which is not constant with depth below extraction zone in terms of a rational water transport model. A closed-form inverse solution is derived which shows uniqueness of model parameter and boundary condition (including paleoprecipitation) estimation, for the specified flow model. Recent expressions of the conventional chloride mass balance technique are derived from the general model presented here; the conventional CMB is shown to be fully compatible with this transient flow model and it requires the steady-state assumption on chloride mass deposition only (and not on water fluxes or boundary conditions). The solutions and results are demonstrated on chloride profile data from west central New Mexico.

Ginn, T.R.; Murphy, E.M.

1996-12-01T23:59:59.000Z

115

Genome Sequence of the Ethene- and Vinyl Chloride-Oxidizing Actinomycete Nocardioides sp Strain JS614  

Science Conference Proceedings (OSTI)

Nocardioides sp. strain JS614 grows on ethene and vinyl chloride (VC) as sole carbon and energy sources and is of interest for bioremediation and biocatalysis. Sequencing of the complete genome of JS614 provides insight into the genetic basis of alkene oxidation, supports ongoing research into the physiology and biochemistry of growth on ethene and VC, and provides biomarkers to facilitate detection of VC/ethene oxidizers in the environment. This is the first genome sequence from the genus Nocardioides and the first genome of a VC/ethene-oxidizing bacterium.

Coleman, Nicholas V [University of Sydney, Australia; Wilson, Neil L [University of Sydney, Australia; Barry, Kerrie [U.S. Department of Energy, Joint Genome Institute; Bruce, David [Los Alamos National Laboratory (LANL); Copeland, A [U.S. Department of Energy, Joint Genome Institute; Dalin, Eileen [U.S. Department of Energy, Joint Genome Institute; Detter, J. Chris [U.S. Department of Energy, Joint Genome Institute; Glavina Del Rio, Tijana [U.S. Department of Energy, Joint Genome Institute; Goodwin, Lynne A. [Los Alamos National Laboratory (LANL); Hammon, Nancy [U.S. Department of Energy, Joint Genome Institute; Han, Shunsheng [Los Alamos National Laboratory (LANL); Hauser, Loren John [ORNL; Israni, Sanjay [U.S. Department of Energy, Joint Genome Institute; Kim, Edwin [U.S. Department of Energy, Joint Genome Institute; Kyrpides, Nikos C [U.S. Department of Energy, Joint Genome Institute; Land, Miriam L [ORNL; Lapidus, Alla L. [U.S. Department of Energy, Joint Genome Institute; Larimer, Frank W [ORNL; Lucas, Susan [U.S. Department of Energy, Joint Genome Institute; Pitluck, Sam [U.S. Department of Energy, Joint Genome Institute; Richardson, Paul [U.S. Department of Energy, Joint Genome Institute; Schmutz, Jeremy [Stanford University; Tapia, Roxanne [Los Alamos National Laboratory (LANL); Thompson, Sue [Los Alamos National Laboratory (LANL); Tice, Hope [U.S. Department of Energy, Joint Genome Institute; Spain, Jim C [Georgia Institute of Technology; Gossett, James G [Cornell University; Mattes, Timothy E [University of Iowa

2011-01-01T23:59:59.000Z

116

Flexible polyvinyl chloride neutron guides for transporting ultracold and very cold neutrons  

SciTech Connect

The transmission of ultracold neutrons (UCNs) through flexible polyvinyl chloride (PVC) tubes with lengths of up to 3 m and an internal diameter of 6-8 mm has been studied. High UCN transmission is found even for arbitrarily bent tubes (single bend, double bend, triple bend, figure eight, etc.). The transmission can be improved significantly by coating the inner surface of the tube with a thin layer of liquid fluorine polymer. The prospects of these neutron guides in fundamental and applied research are discussed.

Arzumanov, S. S., E-mail: sarzumanov@yandex.ru; Bondarenko, L. N. [Russian Research Center Kurchatov Institute (Russian Federation); Geltenbort, P. [Institut Laue-Langevin (France); Morozov, V. I. [Russian Research Center Kurchatov Institute (Russian Federation); Nesvizhevsky, V. V. [Institut Laue-Langevin (France); Panin, Yu. N.; Strepetov, A. N.; Chuvilin, D. Yu. [Russian Research Center Kurchatov Institute (Russian Federation)

2011-12-15T23:59:59.000Z

117

Development of Disposable Sorbents for Chloride Removal from High-Temperature Coal-Derived Gases  

Science Conference Proceedings (OSTI)

The integrated coal-gasification combined-cycle approach is an efficient process for producing electric power from coal by gasification, followed by high-temperature removal of gaseous impurities, then electricity generation by gas turbines. Alternatively, molten carbonate fuel cells (MCFC) may be used instead of gas turbine generators. The coal gas must be treated to remove impurities such as hydrogen chloride (HCl), a reactive, corrosive, and toxic gas, which is produced during gasification from chloride species in the coal. HCl vapor must be removed to meet environmental regulations, to protect power generation equipments such as fuel cells or gas turbines, and to minimize deterioration of hot coal gas desulfurization sorbents. The objectives of this study are to: (1) investigate methods to fabricate reactive sorbent pellets or granules that are capable of reducing HCl vapor in high-temperature coal gas streams to less than 1 ppm in the temperature range 400{degrees}C to 650{degrees}C and the pressure range 1 to 20 atm; (2) testing their suitability in bench-scale fixed- or fluidized-bed reactors; (3) testing a superior sorbent in a circulating fluidized- bed reactor using a gas stream from an operating coal gasifier; and (4) updating the economics of high temperature HCl removal.

Krishnan, G.N.; Canizales, A. [SRI International, Menlo Park, CA (United States); Gupta, R. [Research Triangle Inst., Research Triangle Park, NC (United States); Ayala, R. [General Electric Co., Schenectady, NY (United States). Corporate Research and Development Center

1996-12-31T23:59:59.000Z

118

Open cycle lithium chloride cooling system. Final report, March 1, 1982-May 28, 1983  

DOE Green Energy (OSTI)

A lithium chloride open cycle absorption chiller has been designed, built and tested. Solution reconcentration takes place in a small counter-current packed column supplied with solar heated air. Removal of non-condensable gases that enter the chiller dissolved in the strong solution and the make-up refrigerant streams is accomplished by a liquid-jet ejector and a small vacuum pump. Cooling capacities approaching 1.4 tons and COP levels of 0.58 have been achieved at non-optimum operating conditions. Test results from preliminary system operation suggest that mass transfer processes in both the packed column reconcentrator and the absorber are controlled by concentration gradients in the lithium chloride solution. Liquid phase controlled mass transfer dictates an operating strategy different from the previously assumed gas phase controlled process to obtain maximum rates of evaporation in the packed column. Determination of optimal operating conditions leading to decreased electrical power consumption and improved cooling capacity and coefficient of performance will require further analysis and testing.

Lenz, T. G.; Loef, G. O.G.; Iyer, R.; Wenger, J.

1983-05-01T23:59:59.000Z

119

Molecular Dynamics Simulation of the Transport Properties of Molten Transuranic Chloride Salts  

E-Print Network (OSTI)

The Accelerator Research Laboratory at Texas A&M is proposing a design for accelerator-driven subcritical fission in molten salt (ADSMS), a system that destroys the transuranic elements in used nuclear fuel. The transuranics (TRU) are the most enduring hazard of nuclear power. TRU contain high radiotoxicity and have half-lives of a thousand to a million years. The ADSMS core is fueled by a homogeneous chloride-based molten salt mixture containing TRUCl3 and NaCl. Certain thermodynamic properties are critical to modeling both the neutronics and heat transfer of an ADSMS system. There is a lack of experimental data on the density, heat capacity, electrical and thermal conductivities, and viscosity of TRUCl3 salt systems. Molecular dynamics simulations using a polarizable ion model (PIM) are employed to determine the density and heat capacity of these melts as a function of temperature. Green-Kubo methods are implemented to calculate the electrical conductivity, thermal conductivity, and viscosity of the salt using the outputs of the simulations. Results for pure molten salt systems are compared to experimental data when possible to validate the potentials used. Here I discuss chloride salt systems of interest, their calculated properties, and possible sources of error for our simulations.

Baty, Austin Alan

2013-05-01T23:59:59.000Z

120

DECONTAMINATION OF PLUTONIUM FOR FLUORIDE AND CHLORIDE DURING OXALATE PRECIPITATION, FILTRATION AND CALCINATION PROCESSES  

SciTech Connect

Due to analytical limitations for the determination of fluoride (F) and chloride (Cl) in a previous anion exchange study, an additional study of the decontamination of Pu from F and Cl by oxalate precipitation, filtration and calcination was performed. Anion product solution from the previous impurity study was precipitated as an oxalate, filtered, and calcined to produce an oxide for analysis by pyrohydrolysis for total Cl and F. Analysis of samples from this experiment achieved the purity specification for Cl and F for the proposed AFS-2 process. Decontamination factors (DF's) for the overall process (including anion exchange) achieved a DF of {approx}5000 for F and a DF of {approx}100 for Cl. Similar experiments where both HF and HCl were spiked into the anion product solution to a {approx}5000 {micro}g /g Pu concentration showed a DF of 5 for F and a DF of 35 for Cl across the combined precipitation-filtration-calcination process steps.

Kyser, E.

2012-07-25T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Selective Reduction of Active Metal Chlorides from Molten LiCl-KCl using Lithium Drawdown  

SciTech Connect

In support of optimizing electrorefining technology for treating spent nuclear fuel, lithium drawdown has been investigated for separating actinides from molten salt electrolyte. Drawdown reaction selectivity is a major issue that needs to be investigated, since the goal is to remove actinides while leaving the fission products in the salt. A series of lithium drawdown tests with surrogate fission product chlorides was run to obtain selectivity data with non-radioactive salts, develop a predictive model, and draw conclusions about the viability of using this process with actinide-loadd salt. Results of tests with CsCl, LaCl3, CeCl3, and NdCl3 are reported here. An equilibrium model has been formulated and fit to the experimental data. Excellent fits to the data were achieved. Based on analysis and results obtained to date, it is concluded that clean separation between minor actinides and lanthanides will be difficult to achieve using lithium drawdown.

Michael F. Simpson; Daniel LaBrier; Michael Lineberry; Tae-Sic Yoo

2012-10-01T23:59:59.000Z

122

Methyl Chloride from Direct Methane Partial Oxidation: A High-Temperature Shilov-Like Catalytic System  

SciTech Connect

The intention of this study is to demonstrate and evaluate the scientific and economic feasibility of using special solvents to improve the thermal stability of Pt-catalyst in the Shilov system, such that a high reaction temperature could be achieved. The higher conversion rate (near 100%) of methyl chloride from partial oxidation of methane under the high temperature ({approx} 200 C) without significant Pt0 precipitation has been achieved. High concentration of the Cl- ion has been identified as the key for the stabilization of the Pt-catalysts. H/D exchange measurements indicated that the over oxidation will occur at the elevated temperature, developments of the effective product separation processes will be necessary in order to rationalize the industry-visible CH4 to CH3Cl conversion.

Yongchun Tang; John (Qisheng) Ma

2012-03-23T23:59:59.000Z

123

Tellurite glass as a waste form for a simulated mixed chloride waste stream: Candidate materials selection and initial testing  

Science Conference Proceedings (OSTI)

Tellurite glasses have been researched widely for the last 60 years since they were first introduced by Stanworth. These glasses have been primarily used in research applications as glass host materials for lasers and as non-linear optical materials, though many other uses exist in the literature. Tellurite glasses have long since been used as hosts for various, and even sometimes mixed, halogens (i.e., multiple chlorides or even chlorides and iodides). Thus, it was reasonable to expect that these types of glasses could be used as a waste form to immobilize a combination of mixed chlorides present in the electrochemical separations process involved with fuel separations and processing from nuclear reactors. Many of the properties related to waste forms (e.g., chemical durability, maximum chloride loading) for these materials are unknown and thus, in this study, several different types of tellurite glasses were made and their properties studied to determine if such a candidate waste form could be fabricated with these glasses. One of the formulations studied was a lead tellurite glass, which had a low sodium release and is on-par with high-level waste silicate glass waste forms.

Riley, Brian J.; Rieck, Bennett T.; McCloy, John S.; Crum, Jarrod V.; Sundaram, S. K.; Vienna, John D.

2012-02-02T23:59:59.000Z

124

APPLICATION OF VACUUM SALT DISTILLATION TECHNOLOGY FOR THE REMOVAL OF FLUORIDE AND CHLORIDE FROM LEGACY FISSILE MATERIALS  

Science Conference Proceedings (OSTI)

Between September 2009 and January 2011, the Savannah River National Laboratory (SRNL) and the Savannah River Site (SRS) HB-Line Facility designed, developed, tested, and successfully deployed a production-scale system for the distillation of sodium chloride (NaCl) and potassium chloride (KCl) from plutonium oxide (PuO{sub 2}). Subsequent efforts adapted the vacuum salt distillation (VSD) technology for the removal of chloride and fluoride from less-volatile halide salts at the same process temperature and vacuum. Calcium chloride (CaCl{sub 2}), calcium fluoride (CaF{sub 2}), and plutonium fluoride (PuF{sub 3}) were of particular concern. To enable the use of the same operating conditions for the distillation process, SRNL employed in situ exchange reactions to convert the less-volatile halide salts to compounds that facilitated the distillation of halide without removal of plutonium. SRNL demonstrated the removal of halide from CaCl{sub 2}, CaF{sub 2} and PuF{sub 3} below 1000 C using VSD technology.

Pierce, R.; Peters, T.

2011-11-01T23:59:59.000Z

125

Utility Cycle Testing of a 500-kWh Zinc Chloride Battery at the Battery Energy Storage Test (BEST) Facility  

Science Conference Proceedings (OSTI)

A 500-kWh zinc chloride battery test system completed an entire schedule of 80 simulated utility and customer application cycles--the most diverse and severe known to be successfully performed by any advanced battery system. Encouraged by these results, researchers plan to have a 2-MW demonstration battery system ready for testing in 1986.

1985-10-09T23:59:59.000Z

126

ENGINEERING EXPERIENCE AT BROOKHAVEN NATIONAL LABORATORY IN HANDLING FUSED CHLORIDE SALTS  

SciTech Connect

Two fused chloride salt eutectics, binary LiCl-KCl and ternary NaCl- KCl- MgCl/sub 2/, were used in fuel processing studies as part of the Liquid Metal Fuel Reactor research and development program. Results of engineering work done at Brookhaven since 1950 are summarized. It was demonstrated that fused chloride salt technology is sufficiently developed so that loops and other experimental equipment can be designed and operated at 500 deg C with a high degree of confidence. The equipment, which was operated for many hours, included a large forced-circulation loop and many thermal-convection loops and tanks. The specifications used for the fabrication, cleaning, and testing of equipment for salt service are described. All welded systems, welded by the usual inert-arc procedures, are preferred, but ring type joint stainless-steel flanged connections were found satisfactory, mainly for connecting melt tanks to experimental equipment and for mounting orifice flowmeters. The surfaces of equipment to be used with fused salts were cleaned satisfactorily prior to assembly by several different methods, but sandblasting was found applicable to all types of equipment. Radiography was used to check all welds in contact with fused salt for flaws and, during operation, to locate and determine the cause of any malfunction. Components tested at the normal operating temperature of 500 deg C included pumps, valves, agitators, sightports, samplers, and filtens. Salt samples were usually taken by the thief method. Both stationary and movable resistance type, liquid-level probes were used and were reliable so long as the salt surface remained quiescent; otherwise, splashing and short-circuiting occurred. Nullmatic, pilot-operated pressure transmitters gave good service in conjunction with both orifice and Venturi flowmeters. A procedure is described for preparing pound quantities of pure eutectics, which, in the case of the ternary eutectic, differs from that used in preparing gram quantities. Both eutectics were pretreated with a Bi- Mg-U solution to remove oxidizing impurities before use in corrosion and processing experiments. The results of physical property measurements on the two eutectics are included. (auth)

Raseman, C.J.; Susskind, H.; Farber, G.; McNulty, W.E.; Salzano, F.J.

1960-06-01T23:59:59.000Z

127

Membrane Transport Behavior and the Lability of Chloride on Polyphosphazenes Bearing Bulky Substituents  

SciTech Connect

Polyphosphazenes are an intriguing class of inorganic polymers where much of their functionality is derived from pendant groups attached to phosphorus. The backbone of the polymer consists of alternating phosphorus and nitrogen atoms where the bonding is conventionally drawn as alternating double and single bonds. Orbital nodes are located at each phosphorus atom resulting in electron delocalization between phosphorus atoms, but not through them. Thus, the polymer backbone has a high degree of flexibility where halogens or other leaving groups can be effectively displaced with nucleophiles. In this paper, the first known example of a polyphosphazene with large quantities of non-labile chloride substituents induced by neighboring group steric effects will be discussed. This example is the result of the substitution of poly[bis-chlorophosphazene] with the sodium salt of 3,5-di-tert-butylphenol where only 60% of the chlorines were displaced. This contrasts with the 100% substitution observed with other phenols (phenol, 4-tert-butylphenol, 3-methylphenol, etc.).

Frederick F. Stewart; John R. Klaehn; Christopher J. Orme

2007-08-01T23:59:59.000Z

128

Stabilization of Platinum Nanoparticle Electrocatalysts for Oxygen Reduction Using Poly(diallyldimethylammonium chloride)  

DOE Green Energy (OSTI)

A long-chain polyelectrolyte, poly(diallyldimethylammonium chloride) (PDDA), has been employed to stabilize platinum nanoparticles for oxygen reduction in polymer electrolyte membrane (PEM) fuel cells. Pt nanoparticles were synthesized by reducing H2PtCl6 with NaBH4 in the presence of PDDA and then deposited on carbon support (PDDA-Pt/C). Transmission electron microscope images showed that Pt nanoparticles of PDDA-Pt/C are uniformly dispersed on carbon support with a mean size of about 2.2 nm (2.1 nm for commercial Etek-Pt/C). PDDA-Pt/C exhibited a higher activity towards oxygen reduction reaction (ORR) than Etek-Pt/C. The durability of PDDA-Pt/C was improved by a factor of 2 as compared with Etek-Pt/C. X-ray photoelectron spectroscopy characterization of PDDA-Pt/C revealed the interaction between Pt nanoparticles and PDDA, which increased Pt oxidation potential. PDDA-Nafion ionic crosslinking "entraps" Pt nanoparticles and prevents Pt nanoparticles from migrating/agglomerating on or detaching from carbon support. This provides a promising strategy to improve both the durability and activity of electrocatalysts for fuel cells.

Zhang, Sheng; Shao, Yuyan; Yin, Geping; Lin, Yuehe

2009-10-29T23:59:59.000Z

129

Bench-scale studies of in-duct mercury capture using cupric chloride-impregnated carbons  

Science Conference Proceedings (OSTI)

A brominated activated carbon (Darco Hg-LH) and cupric chloride-impregnated activated carbon (CuCl{sub 2}-ACs) sorbent have been tested in a bench-scale entrained-flow reactor system which was developed for simulating in-flight mercury capture in ducts upstream of particulate matter control devices. The bench-scale experimental system has been operated with the conditions of a residence time of 0.75 s and a gas temperature of 140{sup o}C to simulate typical conditions in the duct of coal-fired exhaust gas. In addition, sorbent deposition on walls which can occur in a laboratory-scale system more than in a full-scale system was significantly reduced so that additional mercury capture by the deposited sorbent was minimized. In the entrained-flow system, CuCl{sub 2}-ACs demonstrated similar performance in Hg adsorption and better performance in Hg{sup 0} oxidation than Darco Hg-LH. In addition, the carbon content of those sorbents was found to determine their Hg adsorption capability in the entrained-flow system. The bench-scale entrained-flow system was able to demonstrate the important Hg adsorption and oxidation characteristics of the tested sorbents. 18 refs., 9 figs., 1 tab.

Sang-Sup Lee; Joo-Youp Lee; Tim C. Keener [University of Cincinnati, Cincinnati, OH (United States). Department of Civil and Environmental Engineering

2009-04-15T23:59:59.000Z

130

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

131

DEVELOPMENT OF DISPOSABLE SORBENTS FOR CHLORIDE REMOVAL FROM HIGH TEMPERATURE COAL-DERIVED GASES  

DOE Green Energy (OSTI)

Advanced integrated-gasification combined-cycle (IGCC) and integrated-gasification fuel cell (IGFC) systems require the development of high temperature sorbents for the removal of hydrogen chloride (HCl) vapor to less than 1 parts-per-million (ppm) levels. HCl is a highly reactive, corrosive, and toxic gas which must be removed to meet environmental regulations, to protect power generation equipment, and to minimize deterioration of hot gas desulfurization sorbents. The objective of this program was to develop disposable, alkali-based sorbents capable of reducing HCl vapor levels to less than 1 ppm in the temperature range from 400 to 750 C and pressures in the range from 1 to 20 atm. The primary areas of focus of this program were to investigate different methods of sorbent fabrication, testing their suitability for different reactor configurations, obtaining reaction kinetics data, and conducting a preliminary economic feasibility assessment. This program was a joint effort between SRI International (SRI), Research Triangle Institute (RTI), and General Electric Corporate Research and Development (GE-CRD). SRI, the prime contractor and RTI, a major subcontractor, performed most of the work in this program. Thermochemical calculations indicated that sodium-based sorbents were capable of reducing HCl vapor levels to less than 1 ppm at temperatures up to 650 C, but the regeneration of spent sorbents would require complex process steps. Nahcolite (NaHCO{sub 3}), a naturally-occurring mineral, could be used as an inexpensive sorbent to remove HCl vapor in hot coal gas streams. In the current program, nahcolite powder was used to fabricate pellets suitable for fixed-bed reactors and granules suitable for fluidized-bed reactors. Pilot-scale equipment were used to prepare sorbents in large batches: pellets by disk pelletization and extrusion techniques, and granules by granulation and spray-drying techniques. Bench-scale fixed- and fluidized-bed reactors were assembled at SRI and RTI to conduct tests at high-temperature, high-pressure conditions (HTHP). The HTHP tests confirmed the ability of nahcolite pellets and granules to reduce the HCl vapor levels to less than 1 ppm levels with a very high sorbent utilization for chloride capture. The effect of several operating variables such as temperature, pressure, presence of hydrogen sulfide, and sorbent preparation methods was studied on the efficacy of HCl removal by the sorbent. Pilot-scale tests were performed in the fluidized-bed mode at the gasifier facility at the GE-CRD. Sorbent exposure tests were also conducted using a hot coal gas stream from the DOE/FETC's fluidized-bed gasifier at Morgantown, WV. These tests confirmed the results obtained at SRI and RTI. A preliminary economic assessment showed that the cost of HCl removal in a commercial IGCC system will be about $0.001/kWh (1 mills/kWh).

Gopala Krishnan; Raghubir Gupta

1999-09-01T23:59:59.000Z

132

Neural Network Modeling of the Lithium/Thionyl Chloride Battery System  

DOE Green Energy (OSTI)

Battery systems have traditionally relied on extensive build and test procedures for product realization. Analytical models have been developed to diminish this reliance, but have only been partially successful in consistently predicting the performance of battery systems. The complex set of interacting physical and chemical processes within battery systems has made the development of analytical models a significant challenge. Advanced simulation tools are needed to more accurately model battery systems which will reduce the time and cost required for product realization. Sandia has initiated an advanced model-based design strategy to battery systems, beginning with the performance of lithiumhhionyl chloride cells. As an alternative approach, we have begun development of cell performance modeling using non-phenomenological models for battery systems based on artificial neural networks (ANNs). ANNs are inductive models for simulating input/output mappings with certain advantages over phenomenological models, particularly for complex systems. Among these advantages is the ability to avoid making measurements of hard to determine physical parameters or having to understand cell processes sufficiently to write mathematical functions describing their behavior. For example, ANN models are also being studied for simulating complex physical processes within the Li/SOC12 cell, such as the time and temperature dependence of the anode interracial resistance. ANNs have been shown to provide a very robust and computationally efficient simulation tool for predicting voltage and capacity output for Li/SOC12 cells under a variety of operating conditions. The ANN modeling approach should be applicable to a wide variety of battery chemistries, including rechargeable systems.

Ingersoll, D.; Jungst, R.G.; O'Gorman, C.C.; Paez, T.L.

1998-10-29T23:59:59.000Z

133

Selected genomic and phenotypic responses of Salmonella serovars to chlorine, chlorine dioxide, and cetylpyridinium chloride  

E-Print Network (OSTI)

Non-typhoidal Salmonella enterica serovars continue to be the leading cause of foodborne illnesses in United States. Chlorine, chlorine related, and quaternary compounds are generally used for disinfecting carcasses and equipment in processing industries. The current study was aimed at understanding the inactivation kinetics of four Salmonella serovars to chlorine, chlorine dioxide and cetylpyridinium chloride (CPC). The transcriptomic responses to oxidative stress was investigated in stationary and log phase cells of S. Typhimurium. The study was also aimed at understanding the effect of the chemicals on the expression of virulence genes associated with the Salmonella Pathogenecity Island 1 (SPI1). The possible induction of the viable but nonculturable (VBNC) state in Salmonella due to CPC was also investigated. The inactivation parameters for each serovar and the chemical were estimated based on the Hom's model, ln (N/N0) = -k C^n T^m and it appeared that while disinfectant contact time was significant, biocide concentration in the overall disinfection was insignificant. This was true especially for chlorine and CPC with subtle differences observed between the serovars. The inactivation efficacy was, however, dependent on both concentration and the exposure time for chlorine dioxide. The highest degree of inactivation was obtained with chlorine followed by chlorine dioxide and CPC. Transcriptomic responses of S. Typhimurium revealed significant downregulation of several metabolic processes such as tricarboxylic acid cycle, oxidative phosphorylation, and amino acid biosynthesis in both log and stationary phase cells. Several stress related genes such as usp, rpoS and ompR were upregulated in the stationary phase cells. Majority of the virulence genes associated with the SPI1 were found to be downregulated for all the treatments. While treatment with chlorine and CPC caused downregulation of all the virulence genes, treatment with chlorine dioxide caused significant upregulation of few (hilC, invC, sipA and sipB) genes associated with the SPI1. Finally, the induction of VBNC state was not concluded as a result of treatment with CPC. However, significant percentage of cells (45 percent) with intact membrane was established based on the BacLight assayTM.

Kakani, Grihalakshmi

2011-05-01T23:59:59.000Z

134

Thermal Analysis of Surrogate Simulated Molten Salts with Metal Chloride Impurities for Electrorefining Used Nuclear Fuel  

SciTech Connect

This project is a fundamental study to measure thermal properties (liquidus, solidus, phase transformation, and enthalpy) of molten salt systems of interest to electrorefining operations, which are used in both the fuel cycle research & development mission and the spent fuel treatment mission of the Department of Energy. During electrorefining operations the electrolyte accumulates elements more active than uranium (transuranics, fission products and bond sodium). The accumulation needs to be closely monitored because the thermal properties of the electrolyte will change as the concentration of the impurities increases. During electrorefining (processing techniques used at the Idaho National Laboratory to separate uranium from spent nuclear fuel) it is important for the electrolyte to remain in a homogeneous liquid phase for operational safeguard and criticality reasons. The phase stability of molten salts in an electrorefiner may be adversely affected by the buildup of fission products in the electrolyte. Potential situations that need to be avoided are: (i) build up of fissile elements in the salt approaching the criticality limits specified for the vessel (ii) freezing of the salts due to change in the liquidus temperature and (iii) phase separation (non-homogenous solution) of elements. 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 work describes the experimental results of typical salts compositions, consisting of chlorides of strontium, samarium, praseodymium, lanthanum, barium, cerium, cesium, neodymium, sodium and gadolinium (as a surrogate for both uranium and plutonium), used in the processing of used nuclear fuels. Differential scanning calorimetry was used to analyze numerous salt samples providing results on the thermal properties. The property of most interest to pyroprocessing is the liquidus temperature. It was previously known the liquidus temperature of the molten salt would change as spent fuel is processed through the Mk-IV electrorefiner. However, the extent of the increase in liquidus temperature was not known. This work is first of its kind in determining thermodynamic properties of a molten salt electrolyte containing transuranics, fission products and bond sodium. Experimental data concluded that the melting temperature of the electrolyte will become greater than the operating temperature of the Mk-IV ER during current fuel processing campaigns. Collected data also helps predict when the molten salt electrolyte will no longer be able to support electrorefining operations.

Toni Y. Gutknecht; Guy L. Fredrickson; Vivek Utgikar

2012-04-01T23:59:59.000Z

135

An In-depth Investigation of an Aluminum Chloride Retarded Mud Acid System on Sandstone Reservoirs  

E-Print Network (OSTI)

Sandstone acidizing using mud acid is a quick and complex process where dissolution and precipitation occur simultaneously. Retarded mud acids are less reactive with the rock reducing the reaction rate hence increased penetration into the formation to remove deep damage. To understand thoroughly the retarded mud acid system, an in-depth investigation of the reaction of HF (hydrofluoric) and H2SiF6 (fluorosilic acid) with alumino silicates and the retarded system is undertaken using coreflood analysis and mineralogy analysis using the inductively coupled plasma. Coreflood analysis is used to understand and investigate the permeability changes in the sandstone rock as the retarded mud acid is injected at different conditions and the inductively coupled plasma (ICP) is used to investigate the effluent samples from the coreflood analysis to properly understand this system. Several issues that have not been addressed previously in literature are identified and discussed, including an optimum flowrate when sandstone is acidized, by acidizing the sandstone rock with a retarded acid system at various flowrates and determining the initial and final permeabilities. Also investigated is the retarded acids compatibility with ferric iron and a comparison of the retarded acid system to regular acid to consequently enable a thorough understanding of the retarded mud acid system using aluminum chloride (AlRMHF). Based on the work done, it is found that the absence of a hydrochloric (HCl) preflush is very detrimental to the sandstone core as calcium fluoride is precipitated and the retarded acid system is found to be compatible with iron(III) as an impurity. The regular acid (RMHF) dissolves considerably more silicon and produces more fines than the AlRMHF. 1cc/min is found to be the optimum flowrate when a sandstone core is acidized with AlRMHF. At this low flowrate, less silicon is dissolved, more aluminum is seen in the effluent and more calcium is dissolved. The retarded aluminum acid system considerably reduces the rate of reaction as evidenced in the dissolution reaction when compared to a regular mud acid system. This reduced rate of reaction implies deeper acid penetration and ultimately deeper damage removal.

Aneto, Nnenna

2012-05-01T23:59:59.000Z

136

Spectroscopy and decay kinetics of Pr{sup 3+}-doped chloride crystals for 1300-nm optical amplifiers  

Science Conference Proceedings (OSTI)

Several Pr{sup 3+}-doped chloride crystals have been tested spectroscopically for suitability as 1300-nm optical amplifiers operating on the {sup 1}G{sub 4} - {sup 3}H{sub 5} transition. {sup 1}G{sub 4} lifetimes are much longer than in fluoride hosts, ranging up to 1300 {mu}sec and suggesting a near-unity luminescence quantum yield. Emission spectra are typically broad (FWHM {approximately} 70 nm) and include the 1310-nm zero-dispersion wavelength of standard telecommunications fiber.

Page, R.H.; Schaffers, K.I.; Wilke, G.D. [and others

1995-03-09T23:59:59.000Z

137

Effect of Organic Acid Additions on the General and Localized Corrosion Susceptibility of Alloy 22 in Chloride Solutions  

Science Conference Proceedings (OSTI)

Electrochemical studies such as cyclic potentiodynamic polarization (CPP) and electrochemical impedance spectroscopy (EIS) were performed to determine the corrosion behavior of Alloy 22 (N06022) in 1M NaCl solutions at various pH values from acidic to neutral at 90 C. All the tested material was wrought Mill Annealed (MA). Tests were also performed in NaCl solutions containing weak organic acids such as oxalic, acetic, citric and picric. Results show that the corrosion rate of Alloy 22 was significantly higher in solutions containing oxalic acid than in solutions of pure NaCl at the same pH. Citric and picric acids showed a slightly higher corrosion rate, and acetic acid maintained the corrosion rate of pure chloride solutions at the same pH. Organic acids revealed to be weak inhibitors for crevice corrosion. Higher concentration ratios, compared to nitrate ions, were needed to completely inhibit crevice corrosion in chloride solutions. Results are discussed considering acid dissociation constants, buffer capacity and complex formation constants of the different weak acids.

Carranza, R M; Giordano, C M; Rodr?guez, M A; Ilevbare, G O; Rebak, R B

2007-08-28T23:59:59.000Z

138

Radiation Stability of Benzyl Tributyl Ammonium Chloride Towards Technetium-99 Extraction  

SciTech Connect

A closed nuclear fuel cycle combining new separation technologies along with generation III and generation IV reactors is a promising way to achieve a sustainable energy supply. But it is important to keep in mind that future recycling processes of used nuclear fuel (UNF) must minimize wastes, improve partitioning process, and integrate waste considerations into processes. New separation processes are being developed worldwide to complement the actual industrialized PUREX process which selectively separates U(VI) and Pu(IV) from the raffinate. As an example, low nitric acid concentration in the aqueous phase of a UREX based process will co-extract U(VI) and Tc(VII) by tri-n-butyl phosphate (TBP). Technetium (Tc-99) is recognized to be one of the most abundant, long-lived radiotoxic isotopes in UNF (half-life, t1/2 = 2.13 × 105 years), and as such, it is targeted in UNF separation strategies for isolation and encapsulation in solid waste forms for final disposal in a nuclear waste repository. Immobilization of Tc-99 by a durable solid waste form is a challenge, and its fate in new advanced technology processes is of importance. It is essential to be able to quantify and locate 1) its occurrence in any new developed flow sheets, 2) its chemical form in the individual phases of a process, 3) its potential quantitative transfer in any waste streams, and consequently, 4) its quantitative separation for either potential transmutation to Ru-100 or isolation and encapsulation in solid waste forms for ultimate disposal. Furthermore, as a result of an U(VI)-Tc(VII) co-extraction in a UREX-based process, Tc(VII) could be found in low level waste (LLW) streams. There is a need for the development of new extraction systems that would selectively extract Tc-99 from LLW streams and concentrate it for feed into high level waste (HLW) for either Tc-99 immobilization in metallic waste forms (Tc-Zr alloys), and/or borosilicate-based waste glass. Studies have been launched to investigate the suitability of new macrocompounds such as crown-ethers, aza-crown ethers, and resorcinarenes for the selective extraction of Tc-99 from nitric acid solutions. The selectivity of the ligand is important in evaluating potential separation processes and also the radiation stability of the molecule is essential for minimization of waste and radiolysis products. In this paper, we are reporting the extraction of TcO4- by benzyltributyl ammonium chloride (BTBA). Experimental efforts were focused on determining the best extraction conditions by varying the ligand’s matrix conditions and concentration, as well as varying the organic phase composition (i.e., diluent variation). Furthermore, the ligand has been investigated for radiation stability. The ?-irradiation was performed on the neat organic phases containing the ligand at different absorbed doses to a maximum of 200 kGy using external Co-60 source. Post-irradiation solvent extraction measurements will be discussed.

Jared Horkley; Audrey Roman; Keri Campbell; Ana Nunez; Amparo Espartero

2013-02-01T23:59:59.000Z

139

Synthesis and characterization of chloride doped polyaniline by bulk oxidative chemical polymerization.Doping effect on electrical conductivity  

E-Print Network (OSTI)

Conductive polymers or "organic metals" are highly engineered nanostructured materials made from organic building blocks. They are candidates as molecular wires for nanotechnology applications in molecular electronics. The conduction in these polymers is due to the presence of delocalized molecular orbitals. In this work, we present the synthesis of chloride doped polyaniline by bulk oxidative chemical polymerization using a solid aniline salt as a monomer instead of liquid aniline to diminish toxic hazards. The FTIR and UV-visible spectra confirmed the expected structure of the polymer. The electrical conductivity measured using a four-probe method was 1.7 S/cm. The dependence of impedance modulus on frequency was measured using an HP impedance analyzer in the range 10 kHz-13 MHz. The influence of doping and the preparation temperature on the electrical conductivity were also investigated.

Yomen Atassi; Mohammad Tally; Mazen Ismail

2008-09-21T23:59:59.000Z

140

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

Note: This page contains sample records for the topic "75-09-2 methylene chloride" from the National Library of EnergyBeta (NLEBeta).
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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

SF 2001-WLD;CONTRACTOR WELDING, CUTTING AND BRAZING  

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

to be burned * Do not use methylene chloride based strippers * Do not use power tools or heat to remove coatings unless certified free of lead, cadmium, lead chromate Is there arc...

142

Cl atom recombination on silicon oxy-chloride layers deposited on chamber walls in chlorine-oxygen plasmas  

SciTech Connect

Chlorine atom recombination coefficients were measured on silicon oxy-chloride surfaces deposited in a chlorine inductively coupled plasma (ICP) with varying oxygen concentrations, using the spinning wall technique. A small cylinder embedded in the walls of the plasma reactor chamber was rapidly rotated, repetitively exposing its surface to the plasma chamber and a differentially pumped analysis chamber housing a quadruple mass spectrometer for line-of-sight desorbing species detection, or an Auger electron spectrometer for in situ surface analysis. The spinning wall frequency was varied from 800 to 30 000 rpm resulting in a detection time, t (the time a point on the surface takes to rotate from plasma chamber to the position facing the mass or Auger spectrometer), of {approx}1-40 ms. Desorbing Cl{sub 2}, due to Langmuir-Hinshelwood (LH) Cl atom recombination on the reactor wall surfaces, was detected by the mass spectrometer and also by a pressure rise in one of the differentially pumped chambers. LH Cl recombination coefficients were calculated by extrapolating time-resolved desorption decay curves to t = 0. A silicon-covered electrode immersed in the plasma was either powered at 13 MHz, creating a dc bias of -119 V, or allowed to electrically float with no bias power. After long exposure to a Cl{sub 2} ICP without substrate bias, slow etching of the Si wafer coats the chamber and spinning wall surfaces with an Si-chloride layer with a relatively small amount of oxygen (due to a slow erosion of the quartz discharge tube) with a stoichiometry of Si:O:Cl = 1:0.38:0.38. On this low-oxygen-coverage surface, any Cl{sub 2} desorption after LH recombination of Cl was below the detection limit. Adding 5% O{sub 2} to the Cl{sub 2} feed gas stopped etching of the Si wafer (with no rf bias) and increased the oxygen content of the wall deposits, while decreasing the Cl content (Si:O:Cl = 1:1.09:0.08). Cl{sub 2} desorption was detectable for Cl recombination on the spinning wall surface coated with this layer, and a recombination probability of {gamma}{sub Cl} = 0.03 was obtained. After this surface was conditioned with a pure oxygen plasma for {approx}60 min, {gamma}{sub Cl} increased to 0.044 and the surface layer was slightly enriched in oxygen fraction (Si:O:Cl = 1:1.09:0.04). This behavior is attributed to a mechanism whereby Cl LH recombination occurs mainly on chlorinated oxygen sites on the silicon oxy-chloride surface, because of the weak Cl-O bond compared to the Cl-Si bond.

Khare, Rohit; Srivastava, Ashutosh; Donnelly, Vincent M. [Department of Chemical and Biomolecular Engineering, University of Houston, Houston, Texas 77204 (United States)

2012-09-15T23:59:59.000Z

143

Electrolytic regeneration of acid cupric chloride printed circuit board etchant. Final report, August 1, 1995--October 31, 1996  

SciTech Connect

The overall objective of this ERIP program was to make substantial progress in further developing a process for electrolytic regeneration of acid cupric chloride etchant - a process which was initially demonstrated in in-house studies and EPA Phase I and Phase II SBIRs. Specific objectives of the work were: (1) to define optimum system operating conditions by conducting a systematic study of process parameters, (2) to develop or find a superior electrolyic cell separator material, (3) to determine an optimum activation procedure for the flow-through carbon/graphite felt electrodes which are so critical to process performance, (4) to demonstrate - on the pre-prototype scale - electrolytic compensation for oxygen ingress - which causes etchant solution growth, and (5) to begin engineering design work on a prototype-scale regeneration unit. Parametric studies looked at the effect that key plating parameters have on copper deposit quality. Parameters tested included (a) velocity past the plating cathodes, (b) copper concentration in the catholyte solution from which the copper is being plated, (c) plating current density, and (d) catholyte cupric ion concentration. The most significant effects were obtained for velocity changes. The work showed that catholyte velocities above 0.5 ft/sec were needed to get adequate plating at 77.5 mA/cm{sup 2} and higher currents, and that even higher flow was better.

Oxley, J.E.; Smialek, R.J.

1997-04-18T23:59:59.000Z

144

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

145

Natrix -Scoring Sheet 1. 0.01 M Mg Chloride, 0.05 M MES pH 5.6, 2.0 M Lithium Sulfate  

E-Print Network (OSTI)

Natrix - Scoring Sheet 1. 0.01 M Mg Chloride, 0.05 M MES pH 5.6, 2.0 M Lithium Sulfate 2. 0.01 M Mg Cacodylate pH 6.0, 1.0 M Lithium Sulfate 12. 0.01 M Mg Sulfate, 0.05 M Na Cacodylate pH 6.0, 1.8 M Lithium pH 6.5, 1.3 M Lithium Sulfate 19. 0.01 M Mg Sulfate, 0.05 M Na Cacodylate pH 6.5, 2.0 M Ammonium

Hill, Chris

146

"Kohn-Shamification" of the classical density-functional theory of inhomogeneous polar molecular liquids with application to liquid hydrogen chloride  

E-Print Network (OSTI)

The Gordian knot of density-functional theories for classical molecular liquids remains finding an accurate free-energy functional in terms of the densities of the atomic sites of the molecules. Following Kohn and Sham, we show how to solve this problem by considering noninteracting molecules in a set of effective potentials. This shift in perspective leads to an accurate and computationally tractable description in terms of simple three-dimensional functions. We also treat both the linear- and saturation- dielectric responses of polar systems, presenting liquid hydrogen chloride as a case study.

Johannes Lischner; T. A. Arias

2008-06-27T23:59:59.000Z

147

[Characterization of historical infiltration in the unsaturated zone at the Nevada Test Site using chloride, bromide, and chlorine-36 as environmental tracers]; [Final subcontract report  

SciTech Connect

This document is an end-of-contract report, prepared by Hydro Geo Chem for Los Alamos National Laboratory under contract number 9-XDD-6329F-1. The ultimate goal of this work is to characterize historical infiltration and unsaturated flow in the Yucca Mountain area of the Nevada Test Site. Work on this contract has focused on using chloride, bromide, stable chlorine isotopes, and chlorine-36 distributions to evaluate the depth of infiltration in the unsaturated zone. Effort in support of this work has included developing analytical procedures, exploring ways in which to separate the. meteoric component from the rock component, and meeting quality assurance requirements.

NONE

1991-05-17T23:59:59.000Z

148

Zn-Doped RuO2 Electrocatalyts for Selective Oxygen Evolution: Relationship Between Local Structure and Electrocatalytic Behavior in Chloride Containing Media  

SciTech Connect

Nanocrystalline electrocatalytically active materials of chemical composition Ru{sub 1-x}Zn{sub x}O{sub 2} (0 < x < 0.3) were synthesized by freeze-drying technique. The diffraction patterns of the prepared samples corresponded to single-phase rutile type oxides.Local structure of the Ru{sub 1-x}Zn{sub x}O{sub 2} based on refinement of Ru K and Zn K edge EXAFS functions shows clustering of the Zn ions in the blocks with ilmenite structure intergrowing with Ru-rich rutile blocks. Ru{sub 1-x}Zn{sub x}O{sub 2} oxides are selective catalysts for anodic oxygen evolution. The selectivity toward oxygen evolution in the presence of chlorides is affected by the actual Zn content and can be ascribed to structural hindrance of the formation of the surface peroxo group based active sites for chlorine evolution. The selectivity toward oxygen evolution in presence of chlorides is accompanied by the drop of the total activity, which gets more pronounced with increasing Zn content.

V Petrykin; K Macounova; J Franc; O Shlyakhtin; M Klementova; S Mukerjee; p Krtil

2011-12-31T23:59:59.000Z

149

A glass-encapsulated calcium phosphate wasteform for the immobilization of actinide-, fluoride-, and chloride-containing radioactive wastes from the pyrochemical reprocessing of plutonium metal  

SciTech Connect

The presence of halide anions in four types of wastes arising from the pyrochemical reprocessing of plutonium required an immobilization process to be developed in which not only the actinide cations but also the halide anions were immobilized in a durable waste form. At AWE, we have developed such a process using Ca3(PO4)2 as the host material. Successful trials of the process with actinide- and Cl-bearing Type I waste were carried out at PNNL where the immobilization of the waste in a form resistant to aqueous leaching was confirmed. Normalized mass losses determined at 40°C and 28 days were 12 x 10-6 g?m-2 and 2.7 x 10-3 g?m-2 for Pu and Cl, respectively. Accelerated radiation-induced damage effects are being determined with specimens containing 238Pu. No changes in the crystalline lattice have been detected with XRD after the 239Pu equivalent of 400 years ageing. Confirmation of the process for Type II waste (a oxyhydroxide-based waste) is currently underway at PNNL. Differences in the ionic state of Pu in the four types of waste have required different surrogates to be used. Samarium chloride was used successfully as a surrogate for both Pu(III) and Am(III) chlorides. Initial investigations into the use of HfO2 as the surrogate for Pu(IV) oxide in Type II waste indicated no significant differences.

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

2007-03-31T23:59:59.000Z

150

Technology Evaluations Related to Mercury, Technetium, and Chloride in Treatment of Wastes at the Idaho Nuclear Technology and Engineering Center of the Idaho National Engineering and Environmental Laboratory  

SciTech Connect

The Idaho High-Level Waste and Facility Disposition Environmental Impact Statement defines alternative for treating and disposing of wastes stored at the Idaho Nuclear Technology and Engineering Center. Development is required for several technologies under consideration for treatment of these wastes. This report contains evaluations of whether specific treatment is needed and if so, by what methods, to remove mercury, technetium, and chlorides in proposed Environmental Impact Statement treatment processes. The evaluations of mercury include a review of regulatory requirements that would apply to mercury wastes in separations processes, an evaluation of the sensitivity of mercury flowrates and concentrations to changes in separations processing schemes and conditions, test results from laboratory-scale experiments of precipitation of mercury by sulfide precipitation agents from the TRUEX carbonate wash effluent, and evaluations of methods to remove mercury from New Waste Calcining Facility liquid and gaseous streams. The evaluation of technetium relates to the need for technetium removal and alternative methods to remove technetium from streams in separations processes. The need for removal of chlorides from New Waste Calcining Facility scrub solution is also evaluated.

C. M. Barnes; D. D. Taylor; S. C. Ashworth; J. B. Bosley; D. R. Haefner

1999-10-01T23:59:59.000Z

151

Removal of Methylene Blue from Aqueous Solutions Using a Novel ...  

Science Conference Proceedings (OSTI)

Conference Tools for 2013 TMS Annual Meeting & Exhibition ... the removal of MB and the state balance of absorption capacity up to 86.89% and 2.6040 mg/g. ... New Development Model for Bauxite Deposits - Dedicated Compact Refinery.

152

Partitioning of mercury, arsenic, selenium, boron, and chloride in a full-scale coal combustion process equipped with selective catalytic reduction, electrostatic precipitation, and flue gas desulfurization systems  

SciTech Connect

A full-scale field study was carried out at a 795 MWe coal-fired power plant equipped with selective catalytic reduction (SCR), an electrostatic precipitator (ESP), and wet flue gas desulfurization (FGD) systems to investigate the distribution of selected trace elements (i.e., mercury, arsenic, selenium, boron, and chloride) from coal, FGD reagent slurry, makeup water to flue gas, solid byproduct, and wastewater streams. Flue gases were collected from the SCR outlet, ESP inlet, FGD inlet, and stack. Concurrent with flue gas sampling, coal, bottom ash, economizer ash, and samples from the FGD process were also collected for elemental analysis. By combining plant operation parameters, the overall material balances of selected elements were established. The removal efficiencies of As, Se, Hg, and B by the ESP unit were 88, 56, 17, and 8%, respectively. Only about 2.5% of Cl was condensed and removed from flue gas by fly ash. The FGD process removed over 90% of Cl, 77% of B, 76% of Hg, 30% of Se, and 5% of As. About 90% and 99% of the FGD-removed Hg and Se were associated with gypsum. For B and Cl, over 99% were discharged from the coal combustion process with the wastewater. Mineral trona (trisodium hydrogendicarbonate dehydrate, Na{sub 3}H(CO{sub 3}){sub 2}.2H{sub 2}O) was injected before the ESP unit to control the emission of sulfur trioxide (SO{sub 3}). By comparing the trace elements compositions in the fly ash samples collected from the locations before and after the trona injection, the injection of trona did not show an observable effect on the partitioning behaviors of selenium and arsenic, but it significantly increased the adsorption of mercury onto fly ash. The stack emissions of mercury, boron, selenium, and chloride were for the most part in the gas phase. 47 refs., 3 figs., 11 tabs.

Chin-Min Cheng; Pauline Hack; Paul Chu; Yung-Nan Chang; Ting-Yu Lin; Chih-Sheng Ko; Po-Han Chiang; Cheng-Chun He; Yuan-Min Lai; Wei-Ping Pan [Western Kentucky University, Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology

2009-09-15T23:59:59.000Z

153

Hydrogen chloride in diffuse interstellar clouds along the line of sight to W31C (G10.6-0.4)  

E-Print Network (OSTI)

We report the detection of hydrogen chloride, HCl, in diffuse molecular clouds on the line of sight towards the star-forming region W31C (G10.6-0.4). The J = 1-0 lines of the two stable HCl isotopologues, H35Cl and H37Cl, are observed using the 1b receiver of the Heterodyne Instrument for the Far-Infrared (HIFI) aboard the Herschel Space Observatory. The HCl line is detected in absorption, over a wide range of velocities associated with di?use clouds along the line of sight to W31C. The analysis of the absorption strength yields a total HCl column density of few 10^13 cm^-2, implying that HCl accounts for ~0.6 % of the total gasphase chlorine, which exceeds by a factor of ~6 the theoretical model predictions. This result is comparable to those obtained from the chemically-related species H2Cl+ and HCl+, for which large column densities have also been reported on the same line of sight. The source of discrepancy between models and observations is still unknown; however, the detection of these Cl-bearing molecu...

Monje, R R; Roueff, E; Gerin, M; De Luca, M; Neufeld, D A; Godard, B; Phillips, T G

2013-01-01T23:59:59.000Z

154

CO2-H2O Mixtures in the Geological Sequestration of CO2. II. Partitioning in Chloride Brines at 12-100 °C and 1-600 bar.  

Office of Scientific and Technical Information (OSTI)

CO CO 2 -H 2 O Mixtures in the Geological Sequestration of CO 2 . II. Partitioning in Chloride Brines at 12-100°C and up to 600 bar. Nicolas Spycher and Karsten Pruess Lawrence Berkeley National Laboratory, MS 90-1116, 1 Cyclotron Road, Berkeley, California, USA September 2004 ABSTRACT Correlations presented by Spycher et al. (2003) to compute the mutual solubilities of CO 2 and H 2 O are extended to include the effect of chloride salts in the aqueous phase. This is accomplished by including, in the original formulation, activity coefficients for aqueous CO 2 derived from several literature sources, primarily for NaCl solutions. Best results are obtained when combining the solubility correlations of Spycher et al. (2003) with the activity coefficient formulation of Rumpf et al. (1994) and Duan and Sun (2003), which

155

Determination of the adsorptive capacity and adsorption isotherm of vapor-phase mercury chloride on powdered activated carbon using thermogravimetric analysis  

Science Conference Proceedings (OSTI)

This study investigated the use of thermogravimetric analysis (TGA) to determine the adsorptive capacity and adsorption isotherm of vapor-phase mercury chloride on powdered activated carbon (PAC). The technique is commonly applied to remove mercury-containing air pollutants from gas streams emitted from municipal solid waste incinerators. An alternative form of powdered activated carbon derived from a pyrolyzed tire char was prepared for use herein. The capacity of waste tire-derived PAC to adsorb vapor-phase HgCl{sub 2} was successfully measured using a self-designed TGA adsorption system. Experimental results showed that the maximum adsorptive capacities of HgCl{sub 2} were 1.75, 0.688, and 0.230 mg of HgCl{sub 2} per gram of powdered activated carbon derived from carbon black at 30, 70, and 150{sup o} for 500 {mu}g/m{sup 3} of HgCl{sub 2}, respectively. Four adsorption isotherms obtained using the Langmuir, Freundlich, Redlich-Peterson, and Brunauer-Emmett-eller (BET) models were used to simulate the adsorption of HgCl{sub 2}. The comparison of experimental data associated with the four adsorption isotherms indicated that BET fit the experimental results better than did the other isotherms at 30{sup o}, whereas the Freundlich isotherm fit the experimental results better at 70 and 150{sup o}. Furthermore, the calculations of the parameters associated with Langmuir and Freundlich isotherms revealed that the adsorption of HgCl{sub 2} by PAC-derived carbon black favored adsorption at various HgCl{sub 2} concentrations and temperatures. 35 refs., 7 figs., 3 tabs.

Hsun-Yu Lin; Chung-Shin Yuan; Wei-Ching Chen; Chung-Hsuang Hung [National Sun Yat-Sen University, Taiwan (China). Institute of Environmental Engineering

2006-11-15T23:59:59.000Z

156

Anisotropy Characterization of I-125 Seed with Attached Encapsulated Cobalt Chloride Complex Contrast Agent Markers for MRI-Based Prostate Brachytherapy  

Science Conference Proceedings (OSTI)

We have developed a novel MRI marker for prostate brachytherapy. The purpose of this study was to evaluate the changes in anisotropy when cobalt chloride complex contrast agent encapsulated contrast agent markers (C4-ECAM) were placed adjacent to an iodine-125 (I-125) titanium seed, and to verify that the C4-ECAMs were visible on magnetic resonance imaging (MRI) after radiation exposure. Two C4-ECAMs were verified to be MRI visible in a phantom before radiation exposure. The C4-ECAMs were then attached to each end of a 12.7-U (10-mCi) I-125 titanium seed in a polymer tube. Anisotropy was measured and analyzed with the seed alone and with attached C4-ECAMs by suspending thermoluminescent dosimeters in a water phantom in 2 circles surrounding the radioactive source with radius of 1 or 2 cm. A T1-weighted MRI evaluation of C4-ECAMs was then performed after exposure to the amount of radiation typically delivered during 1 month of prostate brachytherapy. Measured values of the anisotropy function F(r, {theta}) for the I-125 seed with and without the C4-ECAMs were mutually statistically indistinguishable (standard error of the mean <4.2%) and agreed well with published TG-43 values for the bare seed. As expected, the anisotropy function {phi}{sub an}(r) for the 2 datasets (with and without C4-ECAMs) derived from the measured F(r, {theta}) did not exhibit statistically measurable difference. Both datasets showed agreement with the published TG-43 {phi}{sub an}(r) for the bare seed. The C4-ECAMs were well visualized by MRI after 1 month of radiation exposure. There were no changes in anisotropy when the C4-ECAMs were placed next to an I-125 radioactive seed, and the C4-ECAMs were visualized after radiation exposure.

Frank, Steven J., E-mail: sjfrank@mdanderson.or [Department of Radiation Oncology, University of Texas M. D. Anderson Cancer Center, Houston, TX (United States); Tailor, Ramesh C.; Kudchadker, Rajat J. [Department of Radiation Physics, University of Texas M. D. Anderson Cancer Center, Houston, TX (United States); Martirosyan, Karen S. [Department of Chemical and Biomolecular Engineering, University of Houston, Houston, TX (United States); Stafford, R. Jason; Elliott, Andrew M. [Department of Imaging Physics, University of Texas M. D. Anderson Cancer Center, Houston, TX (United States); Swanson, David A. [Department of Urology, University of Texas M. D. Anderson Cancer Center, Houston, TX (United States); Sing, David; Choi, Jonathan [Department of Radiation Oncology, University of Texas M. D. Anderson Cancer Center, Houston, TX (United States); Mourtada, Firas; Ibbott, Geoffrey S. [Department of Radiation Physics, University of Texas M. D. Anderson Cancer Center, Houston, TX (United States)

2011-07-01T23:59:59.000Z

157

Environmental, health, and safety issues of sodium-sulfur batteries for electric and hybrid vehicles. Volume 3, Transport of sodium-sulfur and sodium-metal-chloride batteries  

DOE Green Energy (OSTI)

This report examines the shipping regulations that govern the shipment of dangerous goods. Since the elemental sodium contained in both sodium-sulfur and sodium-metal-chloride batteries is classified as a dangerous good, and is listed on both the national and international hazardous materials listings, both national and international regulatory processes are considered in this report The interrelationships as well as the differences between the two processes are highlighted. It is important to note that the transport regulatory processes examined in this report are reviewed within the context of assessing the necessary steps needed to provide for the domestic and international transport of sodium-beta batteries. The need for such an assessment was determined by the Shipping Sub-Working Group (SSWG) of the EV Battery Readiness Working Group (Working Group), created in 1990. The Working Group was created to examine the regulatory issues pertaining to in-vehicle safety, shipping, and recycling of sodium-sulfur batteries, each of which is addressed by a sub-working group. The mission of the SSWG is to establish basic provisions that will ensure the safe and efficient transport of sodium-beta batteries. To support that end, a proposal to the UN Committee of Experts was prepared by the SSWG, with the goal of obtaining a proper shipping name and UN number for sodium-beta batteries and to establish the basic transport requirements for such batteries (see the appendix for the proposal as submitted). It is emphasized that because batteries are large articles containing elemental sodium and, in some cases, sulfur, there is no existing UN entry under which they can be classified and for which modal transport requirements, such as the use of packaging appropriate for such large articles, are provided for. It is for this reason that a specific UN entry for sodium-beta batteries is considered essential.

Hammel, C.J.

1992-09-01T23:59:59.000Z

158

Toxicometabolomics approach to urinary biomarkers for mercuric chloride (HgCl{sub 2})-induced nephrotoxicity using proton nuclear magnetic resonance ({sup 1}H NMR) in rats  

Science Conference Proceedings (OSTI)

The primary objective of this study was to determine and characterize surrogate biomarkers that can predict nephrotoxicity induced by mercuric chloride (HgCl{sub 2}) using urinary proton nuclear magnetic resonance ({sup 1}H NMR) spectral data. A procedure for {sup 1}H NMR urinalysis using pattern recognition was proposed to evaluate nephrotoxicity induced by HgCl{sub 2} in Sprague-Dawley rats. HgCl{sub 2} at 0.1 or 0.75 mg/kg was administered intraperitoneally (i.p.), and urine was collected every 24 h for 6 days. Animals (n = 6 per group) were sacrificed 3 or 6 days post-dosing in order to perform clinical blood chemistry tests and histopathologic examinations. Urinary {sup 1}H NMR spectroscopy revealed apparent differential clustering between the control and HgCl{sub 2} treatment groups as evidenced by principal component analysis (PCA) and partial least square (PLS)-discriminant analysis (DA). Time- and dose-dependent separation of HgCl{sub 2}-treated animals from controls was observed by PCA of {sup 1}H NMR spectral data. In HgCl{sub 2}-treated rats, the concentrations of endogenous urinary metabolites of glucose, acetate, alanine, lactate, succinate, and ethanol were significantly increased, whereas the concentrations of 2-oxoglutarate, allantoin, citrate, formate, taurine, and hippurate were significantly decreased. These endogenous metabolites were selected as putative biomarkers for HgCl{sub 2}-induced nephrotoxicity. A dose response was observed in concentrations of lactate, acetate, succinate, and ethanol, where severe disruption of the concentrations of 2-oxoglutarate, citrate, formate, glucose, and taurine was observed at the higher dose (0.75 mg/kg) of HgCl{sub 2}. Correlation of urinary {sup 1}H NMR PLS-DA data with renal histopathologic changes suggests that {sup 1}H NMR urinalysis can be used to predict or screen for HgCl{sub 2}-induced nephrotoxicity{sub .}

Kim, Kyu-Bong, E-mail: kyubong@inje.ac.k [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of); Department of Pharmaceutical Engineering, Inje University, Obang-dong, Gimhae, Gyungnam 621-749 (Korea, Republic of); Um, So Young, E-mail: syum@kfda.go.k [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of); Chung, Myeon Woo, E-mail: mwchung@kfda.go.k [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of); Jung, Seung Chul, E-mail: ipipe4@nate.co [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of); Oh, Ji Seon, E-mail: aquajs24@nate.co [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of); Kim, Seon Hwa, E-mail: hwa2003@kfda.go.k [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of); Na, Han Sung, E-mail: nhk1515@korea.k [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of); Lee, Byung Mu, E-mail: bmlee@skku.ed [College of Pharmacy, Sungkyunkwan University, 300 Cheoncheon-dong, Jangan-gu, Suwon, Gyeonggi-do 440-746 (Korea, Republic of); Choi, Ki Hwan, E-mail: hyokwa11@korea.k [Korea Food and Drug Administration, 5-Nokbun-dong, Eunpyung-gu, Seoul 122-704 (Korea, Republic of)

2010-12-01T23:59:59.000Z

159

Method of separating organic contaminants from fluid feedstreams with polyphosphazene membranes  

DOE Patents (OSTI)

A method is provided for separating polar hydrocarbons from a fluid feedstream. The fluid feedstream is flowed across a first surface of a polyphosphazene semipermeable membrane. At least one polar hydrocarbon from the fluid feedstream permeates through the polyphosphazene semipermeable membrane to a second opposed surface of the semipermeable membrane. Then the permeated polar hydrocarbon is removed from the second opposed surface of the polyphosphazene semipermeable membrane. Outstanding and unexpected separation selectivities on the order of 10,000 were obtained for methylene chloride when a methylene chloride in water feedstream was flowed across the polyphosphazene semipermeable membrane in the invented method.

McCaffrey, R.R.; Cummings, D.G.

1990-12-31T23:59:59.000Z

160

Dehydration of Magnesium Chloride Hexahydrate  

Science Conference Proceedings (OSTI)

Transfer and Consumption of Oxygen in Gold-bearing Sulfide Ores: Agnico-eagle Mines Trials · Tundish Process Performance Improvement: Some Indian Case ...

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161

Technical and economic feasibility of salt-gradient solar ponds at the Truscott Brine Lake of the Red River Chloride Control Project. A report to the House-Senate Committee on Appropriations of the Ninety-Seventh Congress  

DOE Green Energy (OSTI)

The Truscott Brine Lake is being constructed to impound highly brackish water from a number of sources which would normally flow into the Wichita River, a tributary of the Red River in Knox County, Texas. A 35.4-km (22-mile) pipeline is being constructed to carry the brines from their primary source to the Truscott Brine Lake site. The reservoir is designed to contain 100 years of brine emissions from three chloride emission areas in the Wichita River Basin. The solar ponds and power generating facilities would be located in the Bluff Creek Arm of Truscott Brine Lake. The Truscott Brine Lake study includes: survey of suitability of Truscott Lake site, review of solar pond technology, preconceptual design of solar salt pond power plant, and economic evaluation.

Not Available

1982-09-01T23:59:59.000Z

162

[CuCln](2-n) Ion-Pair Species in 1-Ethyl-3-Methylimidazolium Chloride Ionic Liquid-Water Mixtures: Ultraviolet-Visible, X-ray Absorbtion Fine Structure, and Density Functional Theory Characterization  

DOE Green Energy (OSTI)

We report details of the coordination environment about Cu(II) in a pure ionic liquid, 1- ethyl-3-methylimidazolium chloride ([EMIM]Cl) and in mixtures containing varying amounts of water from 0-100% of the [EMIM]Cl. There are many stages in the ion pairing of the divalent cation, Cu(II) including the contact ion pairing of Cu2+ with multiple Cl- to form various CuCln (2-n) polyanions. Thereis also the subsequent solvation and ion pairing of the polychlorometallate anion with the EMIM+ cation. Using a combination of x-ray absorption fine structure (XAFS), UV-Vis spectroscopy and electronic structure calculations (TDDFT) we are able to follow the detailed structural changes about Cu(II). Ion pair formation is strongly promoted in [EMIM]Cl by the low dielectric constant and by the extensive breakdown of the water hydrogen bond network in [EMIM]Cl/water mixtures. In the [EMIM]Cl solvent the CuCl4 2- species dominates and it’s geometry is quite similar to gas-phase structure. These results are important in understanding catalysis and separation processes involving transition metals in ionic liquid systems.

Li, Guosheng; Camaioni, Donald M.; Amonette, James E.; Zhang, Z. Conrad; Johnson, Timothy J.; Fulton, John L.

2010-10-07T23:59:59.000Z

163

from Water and Decolorization of Methylene Blue by Mn3O4-Coated ...  

Science Conference Proceedings (OSTI)

... quantum interference device (SQUID) and nitrogen physical adsorption were ... Electromagnetic Field Shielding Polyurethane Nanocomposites Reinforced ...

164

Surface modification effects on CNTs adsorption of methylene blue and phenol  

Science Conference Proceedings (OSTI)

This study compares the adsorption capacity of modified CNTs using acid and heat treatment. The CNTs were synthesized from acetone and ethanol as carbon sources, using floating catalyst chemical vapor deposition (FC-CVD) method. energy-dispersive X-ray ...

A. H. Norzilah; A. Fakhru'l-Razi; Thomas S. Y. Choong; A. Luqman Chuah

2011-01-01T23:59:59.000Z

165

Molecular Quantum Mechanics 2010: From Methylene to DNA and Beyond Conference Support  

SciTech Connect

This grant was $12500 for partial support of an international conference, Molecular Quantum Mechanics 2010, which was held on the campus of the University of California, Berkeley, from 24 to 29 May 2010. The conference involved more than 250 participants. The conference schedule ran from as early as 8:00 AM to as late as 10:30 PM at night, in order to accommodate six historical lectures, 16 plenary lectures, 42 invited talks and two very strong poster sessions containing 143 contributed posters. Since 1989, the Molecular Quantum Mechanics (MQM) series of international conferences has show- cased the frontiers of research in quantum chemistry with a strong focus on basic theory and algorithms, as well as highlights of topical applications. Both were strongly in evidence at MQM 2010. At the same time as embracing the future, the MQM conferences also honour the lifetime contributions of some of the most prominent scientists in the field of theoretical and computational quantum chemistry. MQM 2010 recognised the work of Prof. Henry F. ‘Fritz’ Schaefer of the Center for Computational Chemistry at the University of Georgia, who was previously on the faculty at Berkeley The travel of invited speakers was partially covered by sponsorships from Dell Computer, Hewlett-Packard, Journal of Chemical Theory and Computation, Virginia Tech College of Science, Molecular Physics, Q-Chem Inc and the American Institute of Physics. By contrast, the conference grant from the Department of Energy was used to provide fellowships and scholarships to enable graduate students and postdoctoral fellows to attend the meeting, and thereby broaden the participation of young scientists at a meeting where in the past most of the attendees have been more senior faculty researchers. We believe that we were very successful in this regard: 118 students and postdocs attended out of the total of 256 participants. In detail, the DOE sponsorship money was partially used for dormitory scholarships that covered the cost of shared accommodation for students and postdocs at Berkeley dormitories. This covered the $200-$305 cost of a shared room for the 5-day duration of the conference. The only condition of these scholarships was that the awardee must present a poster at the meeting. Approximately $7565 was spent for these dormitory scholarships. The remaining expenditures of $4800 was used for 12 merit scholarships which were awarded to students whose poster presentations were judged the best at the conference. This amount covered a significant part of their travel and registration fees.

None

2013-05-15T23:59:59.000Z

166

Experimental Pathology Laboratories, Inc. Vinyl Chloride  

E-Print Network (OSTI)

, and Research (CEDR), Phi Delta Kappa International, 1999. 37. Sorenson SB, Peterson JG, Richardson BA. Child

Bandettini, Peter A.

167

Chloride Depletion in Aged Sea Salt Particles  

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

of how they formed, they transform as they are transported by the wind, showing signs of age by increasing in size, chemical complexity, and oxidation, as well as becoming more...

168

Fluid Bed Dehydration of Magnesium Chloride  

Science Conference Proceedings (OSTI)

... is provided based on open literature sources, including papers and patents. ... Demonstration of Solar-Pumped Laser-Induced Magnesium Production from ...

169

Martian Methyl Chloride. A lesson in uncertainty  

E-Print Network (OSTI)

The MSL Lander Curiosity has recently detected methyl halides coming from heated samples of Martian soil. This is reminiscent of similar findings in the Viking Lander spacecraft. In the 1970s a consensus developed quickly explaining the methyl halides as contamination originating from the spacecraft, and ignoring lines of evidence that the two compounds originated from Mars, and that they could not have originated from the proposed spacecraft chemistry. I discuss why this consensus developed from the understanding of biochemistry and geochemistry of 1976, despite its implausibility. Subsequent explanations for the Viking methyl halides are more plausible but still not proven. The Curiosity rover results are also being explained as a result of on-spacecraft chemistry. I urge caution in this interpretation, in light of the historical Viking example: it is better to leave unexplained data unexplained than to lock in an explanation that precludes future developments.

Bains, William

2013-01-01T23:59:59.000Z

170

Electrochemical Impedance Spectroscopy of Uranium Chloride in ...  

Science Conference Proceedings (OSTI)

Author(s), Kerry Neil Allahar, Michael Shaltry, Mark E Orazem, Darryl P Butt, Supathorn Phongikaroon, Michael Simpson. On-Site Speaker (Planned), Kerry Neil ...

171

Parametric Optimization of the MEO Process for Treatment of Mixed Waste Residues  

Science Conference Proceedings (OSTI)

A series of bench-scale experiments were conducted to determine the optimum reaction conditions for destruction of styrene-divinyl benzene based cation resin and methylene chloride by the mediated electrochemical oxidation (MEO) process. Reaction parameters examined include choice of electron transfer mediator, reaction temperature and solvent system. For the cation exchange resins, maximum destruction efficiencies were obtained using cerium (IV) as mediator in nitric acid at a temperature of 70 C. Reasonable efficiencies were also realized with silver(II) and cobalt (III) at ambient temperature in the same solvent. Use of sulfuric acid as the solvent yielded much lower efficiencies under equivalent conditions. Methylene chloride was found to react only with silver (II) at ambient temperature in nitric acid media, cobalt (III) and cerium (IV) were totally ineffective. These results demonstrate a need to perform bench-scale experiments to determine optimum operating conditions for each organic substrate targeted for treatment by the MEO process.

Cournoyer, M.E.; Smith, W.H.

1999-02-28T23:59:59.000Z

172

Volatiles trapped in coals: Second quarterly report  

SciTech Connect

We have been able to collect and characterize volatiles that are evolved in the grinding of coal. We have developed a very sensitive method for collecting volatiles evolved in grinding. A sealed, gas tight, grinding apparatus has been built. With this system we can collect volatiles freed from the coal matrix during grinding. To do this a 125 cm/sup 3/ sample of coal is placed in to a 1 liter sealable ball mill jar. The jar is evacuated and the coal ground for 1 hr. The jar is then removed from the ball mill and evacuated into our sample collection system. Gas from the jar is pumped through two stages of dust filtering into a liquid nitrogen cold trap charged with 5 ml of methylene chloride. After warming the trap is shaken so that any gas from the sample mixes with and dissolves in the methylene chloride. One microliter samples of the methylene chloride are injected into a Finnegan GCMS. Preliminary analysis of mass spectra from peaks in the RIC show the presence of hydrocarbons. It was possible to definitively identify cyclohexene. The total amount of hydrocarbons seen is low. The attached figure is the mass spectra of the cyclohexene that was collected from the ground coal. 1 fig.

Sutter, J.R.; Halpern, J.B.

1988-01-01T23:59:59.000Z

173

A Thermodynamic Model for Predicting Mineral Reactivity in Supercritical Carbon Dioxide: I. Phase Behavior of Carbon Dioxide - Water - Chloride Salt Systems Across the H2O-Rich to the CO2-Rich Regions  

Science Conference Proceedings (OSTI)

Phase equilibria in mixtures containing carbon dioxide, water, and chloride salts have been investigated using a combination of solubility measurements and thermodynamic modeling. The solubility of water in the CO2-rich phase of ternary mixtures of CO2, H2O and NaCl or CaCl2 was determined, using near infrared spectroscopy, at 90 atm and 40 to 100 °C. These measurements fill a gap in the experimental database for CO2 water salt systems, for which phase composition data have been available only for the H2O-rich phases. A thermodynamic model for CO2 water salt systems has been constructed on the basis of the previously developed Mixed-Solvent Electrolyte (MSE) framework, which is capable of modeling aqueous solutions over broad ranges of temperature and pressure, is valid to high electrolyte concentrations, treats mixed-phase systems (with both scCO2 and water present) and can predict the thermodynamic properties of dry and partially water-saturated supercritical CO2 over broad ranges of temperature and pressure. Within the MSE framework the standard-state properties are calculated from the Helgeson-Kirkham-Flowers equation of state whereas the excess Gibbs energy includes a long-range electrostatic interaction term expressed by a Pitzer-Debye-Hückel equation, a virial coefficient-type term for interactions between ions and a short-range term for interactions involving neutral molecules. The parameters of the MSE model have been evaluated using literature data for both the H2O-rich and CO2-rich phases in the CO2 - H2O binary and for the H2O-rich phase in the CO2 - H2O - NaCl / KCl / CaCl2 / MgCl2 ternary and multicompontent systems. The model accurately represents the properties of these systems at temperatures from 0°C to 300 °C and pressures up to ~4000 atm. Further, the solubilities of H2O in CO2-rich phases that are predicted by the model are in agreement with the new measurements for the CO2 - H2O - NaCl and CO2 - H2O - CaCl2 systems. Thus, the model can be used to predict the effect of various salts on the water content and water activity in CO2-rich phases on the basis of parameters determined from the properties of aqueous systems. Given the importance of water activity in CO2-rich phases for mineral reactivity, the model can be used as a foundation for predicting mineral transformations across the entire CO2/H2O composition range from aqueous solution to anhydrous scCO2. An example application using the model is presented which involves the transformation of forsterite to nesquehonite as a function of temperature and water content in the CO2-rich phase.

Springer, Ronald D.; Wang, Zheming; Anderko, Andre; Wang, Peiming; Felmy, Andrew R.

2012-09-05T23:59:59.000Z

174

Mechanisms of growth inhibition induced by methylene-substituted and ring-substituted dims in breast cancer cells  

E-Print Network (OSTI)

One in 8 women will be diagnosed with breast cancer in the United States and estrogen receptor (ER) status largely influences the type and subsequent success of treatment employed. Although ER-positive breast cancer can be treated with endocrine therapy, the more invasive ER-negative breast cancer is non-responsive to this therapy and cytotoxic agents are often utilized which are associated with many adverse side effects. Consequently, there is a genuine need to develop more effective, less toxic treatments for invasive breast cancer. Indole-3-carbinol is a phytochemical found in cruciferous vegetables and one of its major metabolites, 3,3’-diindolylmethane (DIM), exhibits a broad range of anticancer and antitumorigenic activities. ER-negative MDA-MB-231 and MDA-MB-453 breast cancer cell growth was inhibited after treatment with a novel series of methylenesubstituted DIMs (C-DIMs), namely 1,1-bis(3’-indolyl)-1-(p-substitutedphenyl) methanes containing trifluoromethyl (DIM-C-pPhCF3), t-butyl (DIM-C-pPhtBu) and phenyl (DIM-C-pPhC6H5) groups. In addition, DIM-C-pPhC6H5 (40 mg/kg/d) inhibited tumor growth in nude mice bearing MDA-MB-231 cells as xenografts. Treatment of breast cancer cells with C-DIMs lead to downregulation of cyclin D1 and induction of non-steroidal anti-inflammatory drug-activated gene 1. Detection of necrosis, caspasedependent or caspase-independent apoptosis were not observed in breast cancer cells treated with C-DIMs, however autophagic cell death was induced by C-DIMs. DIM and ring-substituted DIMs have exhibited antitumorigenic activity in tumor murine mammary models. An investigation into the mechanism of cell death induced by DIM and 5,5’-dibromoDIM (5,5’-diBrDIM) in both ER-positive (MCF-7) and ERnegative (MDA-MB-231) breast cancer cells revealed modulation of several key signaling pathways involved in growth control. Both DIM and 5,5’-diBrDIM downregulated cyclin D1, although only 5,5’-diBrDIM induced a depolarization of the mitochondrial membrane. In addition, apoptosis was observed in MCF-7 cells treated with 5,5’-diBrDIM but not MDA-MB-231 cells. In summary, C-DIMs may represent new mechanism-based agents for treatment of breast cancer through induction of autophagic cell death. The ring-substituted DIMs correspond to a novel class of uncharged mitochondrial poisons that are also highly effective in inhibiting breast cancer cell growth. Results of this research provide evidence for the potential role of two new series of DIM analogs for the treatment of highly aggressive breast cancer.

Vanderlaag, Kathryn Elisabeth

2007-05-01T23:59:59.000Z

175

Production of permeable cellulose triacetate membranes  

DOE Patents (OSTI)

A phase inversion process for the preparation of cellulose triacetate (CTA) and regenerated cellulose membranes is disclosed. Such membranes are useful as supports for liquid membranes in facilitated transport processes, as microfiltration membranes, as dialysis or ultrafiltration membranes, and for the preparation of ion-selective electrodes. The process comprises the steps of preparing a casting solution of CTA in a solvent comprising a mixture of cyclohexanone and methylene chloride, casting a film from the casting solution, and immersing the cast film in a methanol bath. The resulting CTA membrane may then be hydrolyzed to regenerated cellulose using conventional techniques.

Johnson, B.M.

1986-12-23T23:59:59.000Z

176

Process for the manufacture of 117Sn diethylenetriaminepentaacetic acids  

DOE Patents (OSTI)

Novel methods are provided for the manufacture of .sup.117m Sn(Sn.sup.4+) DTPA. The method allows the use of DTPA, a toxic chelating agent, in an approximately 1:1 ratio to .sup.117m Sn(Sn.sup.4+) via either aqueous conditions, or using various organic solvents, such as methylene chloride. A pharmaceutical composition manufactured by the novel method is also provided, as well as methods for treatment of bone tumors and pain associated with bone cancer using the pharmaceutical composition of the invention.

Srivastava, Suresh C. (Setauket, NY); Li, Zizhong (Upton, NY); Meinken, George (Middle Island, NY)

2003-01-01T23:59:59.000Z

177

CHLORIDE, IN CALCIUM, IN pH ARSENIC, IN  

E-Print Network (OSTI)

LITER PHAST--A Program for Simulating Ground-Water Flow, Solute Transport, and Multicomponent;COVER ILLUSTRATION: Results of PHAST simulation of the evolution of water chemistry in the CentralH ARSENIC, IN MILLIGRAMS PER LITER MILLIGRAMS PER LITER MICROGRAMS PER LITER #12;PHAST--A Program

178

Modeling of the influence of transverse cracking on chloride ...  

Science Conference Proceedings (OSTI)

... effective diffusion coefficients of concrete bridge decks in Utah [20], likely due to their higher moisture content. 2.3. COMSOL modeling approach ...

2013-08-09T23:59:59.000Z

179

Modeling acid-gas generation from boiling chloride brines  

E-Print Network (OSTI)

of the unsaturated zone at Yucca Mountain, Nevada. J. ofwaste emplacement tunnels at Yucca Mountain, Nevada. J. ofScale Heater Test at Yucca Mountain. International Journal

Zhang, Guoxiang

2010-01-01T23:59:59.000Z

180

Extraction of Titanium and Vanadium by Chloride Leach Processes  

Science Conference Proceedings (OSTI)

... extraction of vanadium from different sources such as ilmenite and oil shales. ... of Ammonium Heptamolybdate Tetrahydrate in Air and Inert Gas Atmospheres.

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

MULTIPHASE REACTOR MODELING FOR ZINC CHLORIDE CATALYZED COAL LIQUEFACTION  

E-Print Network (OSTI)

ix Introduction. A. Coal Liquefaction Overview B.L ZnCl 2-catalyzed Coal Liquefaction . . . . . . . . . • ,Results. . . • . ZnC1 2/MeOH Coal liquefaction Process

Joyce, Peter James

2011-01-01T23:59:59.000Z

182

Chloride Ion Diffusion in Cement-Based Materials ...  

Science Conference Proceedings (OSTI)

... into Hardened Cement Paste , Fly Ash, Silica Fume ... Diffusion Cell: Effects of Material and Test ... LJ, and Yu, SW, Diffusion in Cementitious Materials: II ...

2012-02-23T23:59:59.000Z

183

A COMPREHENSIVE SURVEY OF HYDROGEN CHLORIDE IN THE GALAXY  

SciTech Connect

We report new observations of the fundamental J = 1-0 transition of HCl (at 625.918 GHz) toward a sample of 27 galactic star-forming regions, molecular clouds, and evolved stars, carried out using the Caltech Submillimeter Observatory. Fourteen sources in the sample are also observed in the corresponding H{sup 37}Cl J = 1-0 transition (at 624.978 GHz). We have obtained clear detections in all but four of the targets, often in emission. Absorptions against bright background continuum sources are also seen in nine cases, usually involving a delicate balance between emission and absorption features. From RADEX modeling, we derive gas densities and HCl column densities for sources with HCl emission. HCl is found in a wide range of environments, with gas densities ranging from 10{sup 5} to 10{sup 7} cm{sup -3}. The HCl abundance relative to H{sub 2} is in the range of (3-30) x 10{sup -10}. Comparing with the chlorine abundance in the solar neighborhood, this corresponds to a chlorine depletion factor of up to {approx}400, assuming that HCl accounts for one-third of the total chlorine in the gas phase. The [{sup 35}Cl]/[{sup 37}Cl] isotopic ratio is rather varied, from unity to {approx}5, mostly lower than the terrestrial value of 3.1. Such variation is highly localized, and could be generated by the nucleosynthesis in supernovae, which predicts a {sup 37}Cl deficiency in most models. The lower ratios seen in W3IRS4 and W3IRS5 likely confine the progenitors of the supernovae to stars with relatively large mass ({approx}>25 M{sub sun}) and high metallicity (Z {approx} 0.02).

Peng Ruisheng; Yoshida, Hiroshige; Chamberlin, Richard A. [Caltech Submillimeter Observatory, 111 Nowelo Street, Hilo, HI 96720 (United States); Phillips, Thomas G.; Lis, Dariusz C. [Division of Physics, Mathematics, and Astronomy, 320-47, California Institute of Technology, Pasadena, CA 91125 (United States); Gerin, Maryvonne, E-mail: peng@submm.caltech.ed, E-mail: hiro@submm.caltech.ed, E-mail: cham@astro.caltech.ed, E-mail: tgp@submm.caltech.ed, E-mail: dcl@submm.caltech.ed, E-mail: gerin@lra.ens.f [LERMA-LRA, CNRS, Observatoire de Paris and Ecole Normale Sup'erieure, 24 Rue Lhomond, F 75231 Paris Cedex 05 (France)

2010-11-01T23:59:59.000Z

184

Dual role of nickel in sodium/nickel chloride batteries  

DOE Green Energy (OSTI)

Corrosion of Ni metal in chloroaluminate melts containing sulfur additive was investigated in order to see whether Ni could be used not only as active material but also as current collector and cell- case material. Three layers were found after three days; they comprised NiCl{sub 2}, Ni sulfide, and NaAlCl{sub 4}. Ni-200 wires were also tested under tension in NaAlCl{sub 4} + 2 wt%S at 300 C; no stress corrosion was observed. Results show that Ni metal is very stable. 9 refs, 3 figs. (DLC)

Prakash, J.; Redey, L.; Skocypec, R.; Lowrey, R.; Vissers, D.

1992-01-01T23:59:59.000Z

185

MULTIPHASE REACTOR MODELING FOR ZINC CHLORIDE CATALYZED COAL LIQUEFACTION  

E-Print Network (OSTI)

farth- est along is the Exxon Donor Solvent process, whichCoal, I and II Process Exxon Donor Solvent B. ZnC1 2-mentioned above~ the Exxon development has included the use

Joyce, Peter James

2011-01-01T23:59:59.000Z

186

A Novel Low-Cost Sodium-Zinc Chloride Battery  

Science Conference Proceedings (OSTI)

The sodium-metal halide (ZEBRA) battery has been considered as one of the most attractive energy storage systems for stationary and transportation applications. Even though Na-NiCl2 battery has been widely investigated, there is still a need to develop a more economical system to make this technology more attractive for commercialization. In the present work, a novel low-cost Na-ZnCl2 battery with a thin planar ??-Al2O3 solid electrolyte (BASE) was proposed, and its electrochemical reactions and battery performance were investigated. Compared to the Na-NiCl2 chemistry, the ZnCl2-based chemistry was more complicated, in which multiple electrochemical reactions including liquid-phase formation occurred at temperatures above 253°C. During the first stage of charge, NaCl reacted with Zn to form Na in the anode and Na2ZnCl4 in the cathode. Once all the residual NaCl was consumed, further charging led to the formation of a NaCl-ZnCl2 liquid phase. At the end of charge, the liquid phase reacted with Zn to produce solid ZnCl2. To identify the effects of liquid-phase formation on electrochemical performance, button cells were assembled and tested at 280°C and 240°C. At 280°C where the liquid phase formed during cycling, cells revealed quite stable cyclability. On the other hand, more rapid increase in polarization was observed at 240°C where only solid-state electrochemical reactions occurred. SEM analysis indicated that the stable performance at 280°C was due to the suppressed growth of Zn and NaCl particles, which were generated from the liquid phase during discharge of each cycle.

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

2013-02-28T23:59:59.000Z

187

Modeling acid-gas generation from boiling chloride brines  

E-Print Network (OSTI)

first drop" of condensate from superheated geothermal steam.from the steam flowing above the condensate. Incompletecondensate that forms at dew-point temperature through expansion of superheated geothermal steam,

Zhang, Guoxiang

2010-01-01T23:59:59.000Z

188

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

189

MULTIPHASE REACTOR MODELING FOR ZINC CHLORIDE CATALYZED COAL LIQUEFACTION  

E-Print Network (OSTI)

II. c. High Yield Batch Reactor Results. . . • .Objectives •. Slurry Reactors . . . . . . .A. StudiesSystems. D. Slurry Reactor Theory. General. . Application to

Joyce, Peter James

2011-01-01T23:59:59.000Z

190

The Thermodynamics of Gaseous, Cuprous Chloride Monomer and Trimer  

E-Print Network (OSTI)

No.W-7405-eng~48B TIiE THERMODYNAMICS OF GASEOUS" CUPROUSCu(s) + HCl::= I Thermodynamics of Vaporization to Monomeric

Brewer, Leo

2010-01-01T23:59:59.000Z

191

Modeling acid-gas generation from boiling chloride brines  

E-Print Network (OSTI)

when steam flows through a condenser with incomplete or pooral. [6]). A water-cooled condenser was attached at the topin both the flask and condenser. Towards the end of the

Zhang, Guoxiang

2010-01-01T23:59:59.000Z

192

Chloride Leaching of Spent Lead-Acid Battery Paste  

Science Conference Proceedings (OSTI)

Abstract Scope, In this study leaching of spent lead acid-battery paste in sodium ... Cost, Energy, Emissions, and Resource Assessment of the Production of ...

193

C1 Technology of Molten salt Electrolysis of Magnesium Chloride  

Science Conference Proceedings (OSTI)

D14 Gold Nanoparticles in Red Ruby Glasses Used for Decoration in Thailand · D15 Soft Magnetic Properties of Nanocrystalline Fe-based P/M Cores Mixed ...

194

Influence of Chloride Ions as Contaminants on the Corrosion ...  

Science Conference Proceedings (OSTI)

Crack Growth Rates of Irradiated Commercial Stainless Steels in BWR and PWR ... Detailed Root Cause Analysis of SG Tube ODSCC Indications within the Tube Sheets of NPP Biblis Unit A .... Radiation Damage in Fe-C-Met Model Alloys ... Stress Corrosion Cracking Behavior near the Fusion Boundary of Dissimilar Weld

195

Gold Preg-Robbing by Silicates in Chloride Media  

Science Conference Proceedings (OSTI)

Evolution of Gold Gravity Recovery in Grinding Circuits - A Critical Review ... Selective Separations of Gold and Contaminants from Various Gold and Silver ...

196

Uranium chloride extraction of transuranium elements from LWR ...  

A process of separating transuranium actinide values from uranium values present in spent nuclear oxide fuels containing rare earth and noble metal ...

197

Modeling chloride transport in cracked concrete: a 3-D image ...  

Science Conference Proceedings (OSTI)

... and Technology, 100 Bureau Drive 8615, Gaithersburg ... package implements the UMFPACK direct solver ... on a rotating anode generator and capillary ...

2013-01-07T23:59:59.000Z

198

MULTIPHASE REACTOR MODELING FOR ZINC CHLORIDE CATALYZED COAL LIQUEFACTION  

E-Print Network (OSTI)

of noble gases in molten salts, which also provide a modeln Hexane B2 275°C. Hydrogen-Molten Salt WI (dynes/em) WI PI

Joyce, Peter James

2011-01-01T23:59:59.000Z

199

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

200

Electrochemical Studies and Analysis of Uranium Chloride in Molten ...  

Science Conference Proceedings (OSTI)

Abstract Scope, The redox reactions of uranium on a tungsten electrode versus reference ... Cathodic Behavior of Silicon (?) in BaF2-CaF2 –SiO2 Melts.

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

An integrated model of the lithium/thionyl chloride battery  

DOE Green Energy (OSTI)

The desire to reduce the time and cost of design engineering on new components or to validate existing designs in new applications is stimulating the development of modeling and simulation tools. The authors are applying a model-based design approach to low and moderate rate versions of the Li/SOCl{sub 2} D-size cell with success. Three types of models are being constructed and integrated to achieve maximum capability and flexibility in the final simulation tool. A phenomenology based electrochemical model links performance and the cell design, chemical processes, and material properties. An artificial neural network model improves computational efficiency and fills gaps in the simulation capability when fundamental cell parameters are too difficult to measure or the forms of the physical relationships are not understood. Finally, a PSpice-based model provides a simple way to test the cell under realistic electrical circuit conditions. Integration of these three parts allows a complete link to be made between fundamental battery design characteristics and the performance of the rest of the electrical subsystem.

Jungst, R.G.; Nagasubramanian, G.; Ingersoll, D.; O`Gorman, C.C.; Paez, T.L. [Sandia National Labs., Albuquerque, NM (United States); Jain, M.; Weidner, J.W. [Univ. of South Carolina, Columbia, SC (United States)

1998-06-08T23:59:59.000Z

202

Electrochemical and Thermal Properties of Rare-Earth Chlorides in ...  

Science Conference Proceedings (OSTI)

Radioactive Demonstrations of Fluidized Bed Steam Reforming (FBSR) with Hanford Low Activity Wastes · Radionuclide Behavior and Geochemistry in Boom  ...

203

Spouted Bed Electrowinning of Zinc from Chloride Electrolytes  

Science Conference Proceedings (OSTI)

Aug 1, 2000 ... Current efficiencies, for the cell with the SBE, have been as high as 90% and DC energy consumption as Iow as 2.8 kWh/kg zinc deposited.

204

Mixed Waste Management Facility (MWMF) groundwater monitoring report. Fourth quarter 1993 and 1993 summary  

Science Conference Proceedings (OSTI)

During fourth quarter 1993, 10 constituents exceeded final Primary Drinking Water Standards in groundwater samples from downgradient monitoring wells at the Mixed Waste Management Facility, the Old Burial Ground, the E-Area Vaults, and the proposed Hazardous Waste/Mixed Waste Disposal Vaults. As in previous quarters, tritium and trichloroethylene were the most widespread elevated constituents. Carbon tetrachloride, chloroform, chloroethane (vinyl chloride), 1,1-dichloroethylene, dichloromethane (methylene chloride), lead, mercury, or tetrachloroethylene also exceeded standards in one or more wells. Elevated constituents were found in numerous Aquifer Zone 2B{sub 2} (Water Table) and Aquifer Zone 2B{sub 1}, (Barnwell/McBean) wells and in two Aquifer Unit 2A (Congaree) wells. The groundwater flow direction and rates in the three hydrostratigraphic units were similar to those of previous quarters.

Butler, C.T.

1994-03-01T23:59:59.000Z

205

U.S. Department of Energy Categorical Exclusion Determination Form  

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

Analysis of Organic Species by Gas Chromatography (GC) and Gas Chromatography/Mass Spectrometry (GC/MS) Analysis of Organic Species by Gas Chromatography (GC) and Gas Chromatography/Mass Spectrometry (GC/MS) Savannah River Site Aiken/Aiken/South Carolina This activity has been carried for nineteen years, and the activity will not change significantly from how it was done in the past. Instruments designated as Gas Chromatograph / Mass Spectrometers (GC/MS) are used in the Analytical Development Section (ADS) for the analysis of organic materials in solids, liquids, or gases. The instruments use helium carrier gas and thermal adsorption/desorption to separate analytes, and mass spectrometers to detect the analytes, once separated. Sample preparation uses methylene chloride for extraction of organic analytes from solid and liquid samples, and the solvent is evaporated to concentrate analytes prior to analysis in accordance with EPA regulatory protocol.

206

Heavy Oil Process Monitor: Automated On-Column Asphaltene Precipitation and Re-Dissolution  

Science Conference Proceedings (OSTI)

An automated separation technique was developed that provides a new approach to measuring the distribution profiles of the most polar, or asphaltenic components of an oil, using a continuous flow system to precipitate and re-dissolve asphaltenes from the oil. Methods of analysis based on this new technique were explored. One method based on the new technique involves precipitation of a portion of residua sample in heptane on a polytetrafluoroethylene-packed (PTFE) column. The precipitated material is re-dissolved in three steps using solvents of increasing polarity: cyclohexane, toluene, and methylene chloride. The amount of asphaltenes that dissolve in cyclohexane is a useful diagnostic of the thermal history of oil, and its proximity to coke formation. For example, about 40 % (w/w) of the heptane asphaltenes from unpyrolyzed residua dissolves in cyclohexane. As pyrolysis progresses, this number decrease to below 15% as coke and toluene insoluble pre-coke materials appear. Currently, the procedure for the isolation of heptane asphaltenes and the determination of the amount of asphaltenes soluble in cyclohexane spans three days. The automated procedure takes one hour. Another method uses a single solvent, methylene chloride, to re-dissolve the material that precipitates on heptane on the PTFE-packed column. The area of this second peak can be used to calculate a value which correlates with gravimetric asphaltene content. Currently the gravimetric procedure to determine asphaltenes takes about 24 hours. The automated procedure takes 30 minutes. Results for four series of original and pyrolyzed residua were compared with data from the gravimetric methods. Methods based on the new on-column precipitation and re-dissolution technique provide significantly more detail about the polar constituent's oils than the gravimetric determination of asphaltenes.

John F. Schabron; Joseph F. Rovani; Mark Sanderson

2007-03-31T23:59:59.000Z

207

Methyl chloride via oxyhydrochlorination of methane. Quarterly technical progress report No. 10, January 1944--March 1994  

SciTech Connect

In work related to the design and construction of the Process Development Unit (PDU) this quarter involved further detail design and a real start to the construction activities. Status updates are given below for each discipline in the Task 2.0 and 3.0 headings. This work is progressing well. with the caveat of several small slips in the scheduling. On the catalyst development front this quarter was extremely productive. Many catalyst screening experiments were completed and they showed that control of the reaction exotherm is going to be quite challenging under PDU conditions. The presence of much more efficient reactor design and the ability to maintain closer to isothermal conditions is expected to give a significant advantage in actual PDU operation. A major concern at the moment is the cost of La in the catalyst being used. An action plan to remedy this is being put together.

NONE

1994-08-01T23:59:59.000Z

208

COAL LIQUEFACTION USING ZINC CHLORIDE CATALYST IN AN EXTRACTING SOLVENT MEDIUM  

E-Print Network (OSTI)

Rate Data o a o u a a Catalyst Loading • . Reaction Time . •and Pressure Effect of CO-catalysts and Additives .Co-catalysts • • a. Zinc Metal • b. Nickel and Nickel

Gandhi, Shamim Ahmed

2013-01-01T23:59:59.000Z

209

STUDIES OF MICROMORPHOLOGY AND CURRENT EFFICIENCY OF ZINC ELECTRODEPOSITED FROM FLOWING CHLORIDE ELECTROLYTES  

E-Print Network (OSTI)

Battery Systems Purpose and Scope of this Study .. Literature Review . 13 Recent Historybattery (11) L5 r XBB II. LITERATURE REVIEW Recent History

Mc Vay, L.

2011-01-01T23:59:59.000Z

210

Densities in the Liquid Hydrogen Chloride Solvent System Heather Brooks Shapiro and Donald R. Sadoway*  

E-Print Network (OSTI)

for electrodeposition of several reactive metals and silicon from liquefied halogenous gases at subambient temperatures requires more cooling power than simple dry ice slush baths but much less than standard liquid nitrogen

Sadoway, Donald Robert

211

Calibration of Yucca Mountain unsaturated zone flow and transport model using porewater chloride data  

E-Print Network (OSTI)

of hydrogeologic units at Yucca Mountain, Nevada. U.S.infiltration for the Yucca Mountain Area, Nevada. Milestonethe unsaturated zone at Yucca Mountain, Nevada. J. Contam.

Liu, Jianchun; Sonnenthal, Eric L.; Bodvarsson, Gudmundur S.

2002-01-01T23:59:59.000Z

212

The impact of improved materials in poly(vinyl chloride)-based endotracheal tubes  

E-Print Network (OSTI)

Endotracheal tubes (ETs) are used to aid artificial ventilation in millions of medical patients every year and are known to invoke the proliferative phase in the cell linings. The technical objective of this work was to ...

Domike, Kristin Rebecca, 1981-

2004-01-01T23:59:59.000Z

213

Analysis of chlorinated polyvinyl chloride pipe burst problems :Vasquez residence system inspection.  

DOE Green Energy (OSTI)

This report documents the investigation regarding the failure of CPVC piping that was used to connect a solar hot water system to standard plumbing in a home. Details of the failure are described along with numerous pictures and diagrams. A potential failure mechanism is described and recommendations are outlined to prevent such a failure.

Black, Billy D.; Menicucci, David F.; Harrison, John (Florida Solar Energy Center)

2005-10-01T23:59:59.000Z

214

Regenerable Sorbent Development for Sulfur, Chloride and Ammonia Removal from Coal-Derived Synthesis Gas  

DOE Green Energy (OSTI)

A large number of components in coal form corrosive and toxic compounds during coal gasification processes. DOE’s NETL aims to reduce contaminants to parts per billion in order to utilize gasification gas streams in fuel cell applications. Even more stringent requirements are expected if the fuel is to be utilized in chemical production applications. Regenerable hydrogen sulfide removal sorbents have been developed at NETL. These sorbents can remove the hydrogen sulfide to ppb range at 316 °C and at 20 atmospheres. The sorbent can be regenerated with oxygen. Reactivity and physical durability of the sorbent did not change during the multi-cycle tests. The sorbent development work has been extended to include the removal of other major impurities, such as HCl and NH3. The sorbents for HCl removal that are available today are not regenerable. Regenerable HCl removal sorbents have been developed at NETL. These sorbents can remove HCl to ppb range at 300 °C to 500 °C. The sorbent can be regenerated with oxygen. Results of TGA and bench-scale flow reactor tests with both regenerable and non-regenerable HCl removal sorbents will be discussed in the paper. Bench-scale reactor tests were also conducted with NH3 removal sorbents. The results indicated that the sorbents have a high removal capacity and good regenerability during the multi-cycle tests. Future emphasis of the NETL coal gasification/cleanup program is to develop multi-functional sorbents to remove multiple impurities in order to minimize the steps involved in the cleanup systems. To accomplish this goal, a regenerable sorbent capable of removing both HCl and H2S was developed. The results of the TGA conducted with the sorbent to evaluate the feasibility of both H2S and HCl sorption will be discussed in this paper.

Siriwardane, R.V.; Tian, H.; Simonyi, T.; Webster, T.

2007-08-01T23:59:59.000Z

215

Comparative Neurotoxicity of Methylmercury and Mercuric Chloride In Vivo and In Vitro  

E-Print Network (OSTI)

It is impossible to remove methylmercury (MeHg) from biological systems because MeHg is found throughout our environment in many fresh and salt water fish. The consumption of fish is important to human nutrition and health. The mechanism of MeHg neurotoxicity must be understood to minimize adverse exposure consequences. The dissertation objective was to: 1) compare mechanisms of MeHg neurotoxicity between animals exposed as adults and those exposed during gestation, and 2) develop an in vitro test model of in vivo MeHg exposure. Total mercury (Hg) levels in tissue / cells were determined by combustion / trapping / atomic absorption. Cell death was determined by Fluoro-Jade histochemical staining and activated caspase 3 immunohistochemistry for in vivo studies, and Trypan blue exclusion, lactate dehydrogenase activity, and cytotoxicity assays for in vitro studies. Mitochondrial membrane potential (MMP), intracellular calcium ion concentration ([Ca2+]i), and production of reactive oxygen species (ROS) were determined using fluorescence microscopy or microplate reader assays. Young adult C57Bl/6 mice were exposed to a total dose of 0, 1.0, or 5.0 mg/kg body weight MeHg divided over postnatal days (P)35 to 39. Pregnant female mice were exposed to a total does of 0, 0.1, or 1.0 mg/kg body weight MeHg divided over gestational days (G)8 to 18. SY5Y cells were exposed to 0, 0.01, 0.1, or 1.0 ?M MeHg or HgCl2 for 24, 48, or 72 hours. Total Hg in brains of young adult mice, mouse pups, and SY5Y cells accumulated in a dose-dependent manner. Cell death increased in SY5Y cells exposed to the highest concentrations of MeHg and HgCl2 used in this study. Cell death increased in the molecular and granule cerebellar cell layers of young adult mice exposed to the highest doses of MeHg used in this study. P0 mouse pups showed no increase in cell death within the cerebellum following MeHg exposure. Cerebella of mice at P10 exhibited decreased dying cells only in the external germinal layer. Low concentrations of MeHg affected MMP in both in vivo and in vitro studies, but did not result in decreased MMP typically associated with higher MeHg concentrations. [Ca2+]i was increased throughout the in vivo experiments in an age- , sexand brain region-dependent manner. Generation of ROS was decreased in both in vivo and in vitro studies with both the MeHg and HgCl2 (in vitro) treatments. In summary, low and moderate MeHg exposure, both in vivo and in vitro, altered mitochondrial function, Ca2+ homeostasis, and ROS differently than what is reported in the literature for higher MeHg exposure concentrations. SY5Y cells were sensitive to low-levels of MeHg and HgCl2 and responded similarly to cells in the whole animal studies, thus making SY5Y cells realistic candidates for mechanistic MeHg studies. Cell culture and whole animal neuronal functional studies at chronic low-level MeHg exposure are limited. These data suggest that low-levels of MeHg may affect neuronal function. Therefore, further chronic low-level MeHg neuronal functional studies are warranted.

Thuett, Kerry A.

2009-08-01T23:59:59.000Z

216

Interactions of chlorine plasmas with silicon chloride-coated reactor walls during and after silicon etching  

SciTech Connect

The interplay between chlorine inductively coupled plasmas (ICP) and reactor walls coated with silicon etching products has been studied in situ by Auger electron spectroscopy and line-of-sight mass spectrometry using the spinning wall method. A bare silicon wafer mounted on a radio frequency powered electrode (-108 V dc self-bias) was etched in a 13.56 MHz, 400 W ICP. Etching products, along with some oxygen due to erosion of the discharge tube, deposit a Si-oxychloride layer on the plasma reactor walls, including the rotating substrate surface. Without Si-substrate bias, the layer that was previously deposited on the walls with Si-substrate bias reacts with Cl-atoms in the chlorine plasma, forming products that desorb, fragment in the plasma, stick on the spinning wall and sometimes react, and then desorb and are detected by the mass spectrometer. In addition to mass-to-charge (m/e) signals at 63, 98, 133, and 168, corresponding to SiCl{sub x} (x = 1 - 4), many Si-oxychloride fragments with m/e = 107, 177, 196, 212, 231, 247, 275, 291, 294, 307, 329, 345, 361, and 392 were also observed from what appear to be major products desorbing from the spinning wall. It is shown that the evolution of etching products is a complex 'recycling' process in which these species deposit and desorb from the walls many times, and repeatedly fragment in the plasma before being detected by the mass spectrometer. SiCl{sub 3} sticks on the walls and appears to desorb for at least milliseconds after exposure to the chlorine plasma. Notably absent are signals at m/e = 70 and 72, indicating little or no Langmuir-Hinshelwood recombination of Cl on this surface, in contrast to previous studies done in the absence of Si etching.

Khare, Rohit; Srivastava, Ashutosh; Donnelly, Vincent M. [Department of Chemical and Biomolecular Engineering, University of Houston, Houston, Texas 77204 (United States)

2012-09-15T23:59:59.000Z

217

STUDIES OF MICROMORPHOLOGY AND CURRENT EFFICIENCY OF ZINC ELECTRODEPOSITED FROM FLOWING CHLORIDE ELECTROLYTES  

E-Print Network (OSTI)

the rechargeable zinc/chlorine and zinc/bromine batteriesthis section. The zinc/chlorine and zinc/bromine batteriesare high: 2.32 V for the chlorine (12) and tions are 1.85 V

Mc Vay, L.

2011-01-01T23:59:59.000Z

218

A New Redox Flow Battery Using Fe/V Redox Couples in Chloride ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, Materials Science & Technology 2011. Symposium, Energy Storage: Materials, Systems and Applications. Presentation Title, A ...

219

COAL LIQUEFACTION USING ZINC CHLORIDE CATALYST IN AN EXTRACTING SOLVENT MEDIUM  

E-Print Network (OSTI)

2-1 Figure Schematic of the Exxon Donor Solvent Process forL.W. , and Wilson, E.L. Exxon Donor Solvent Process 1 CEP 1commercialization are (1) the Exxon Donor Solvent process, (

Gandhi, Shamim Ahmed

2013-01-01T23:59:59.000Z

220

COAL LIQUEFACTION USING ZINC CHLORIDE CATALYST IN AN EXTRACTING SOLVENT MEDIUM  

E-Print Network (OSTI)

1978) Richardson, F.W. Oil from Coal, Chemical TechnologyStatus of Coal and Oil Shale Conversion, University of Utah,of increasing the yield of oil like products. In contrast,

Gandhi, Shamim Ahmed

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

The Role of Boron-Chloride and Noble Gas Isotope Ratios in TVZ Geothermal Systems  

DOE Green Energy (OSTI)

The model of the geothermal system in which deep circulating groundwater containing noble gases, at air saturated water concentrations, mixes with hot fluids of mantle origin at depth, is extended to include the effect of interaction of the ascending fluid with both solid and gaseous phases of basement (or other) rocks en route to the surface. It is demonstrated that this interaction is responsible for most of the CO{sub 2} in the Taupo Volcanic Zone (TVZ) geothermal systems. It is proposed that the modeling of this interaction might be accomplished by techniques similar to those used for the understanding of the oxygen isotope shift found in geothermal systems. The water rock interaction experiments of Ellis and Mahon (1964, 1967) provides some data on the kinetic rates for B and Cl dissolution from rocks likely to be encountered in the geothermal system, but further information on the behavior of B may be needed. If these problems can be overcome this modeling technique has promise for the estimation of the recharge of geothermal systems and hence the sustainability of these systems.

Hulston, J.R.

1995-01-01T23:59:59.000Z

222

Palladium chloride to palladium metal two-dimensional nucleation and growth phenomena  

SciTech Connect

The reduction of a monolayer of surface-bound Pd(II) to Pd(0) on a palladium substrate reveals two-dimensional nucleation and growth phenomena. Using well-known 2D nucleation-growth theories, this reduction is shown to proceed by an instantaneous nucleation and growth mechanism. However, when a submonolayer of Pd(II) is present, this mechanism fails to account for the experimentally observed high cathodic currents seen at zero time. A model incorporating preexisting Pd(0) cylindrical sites on the partially oxidized Pd(0) surface has been successfully applied to account for the discrepancy between the experimental results and current 2D theories. Using this modified 2D model, values for the mathematical product of cylindrical growth rate and the square root of the nucleation site densities have been determined, and the overpotential dependence of the growth rate has been confirmed and quantified. These 2D nucleation-growth phenomena have practical consequences on the performance of the Pd(II)/Pd(0) system as a faradaic supercapacitor, and probably on the performance of other 2D faradaic supercapacitor systems. In addition, because many electrodes undergo monolayer surface oxidation-reduction reactions in other solvent systems, especially aqueous electrolytes, these 2D nucleation-growth phenomena may play a role in these important surface-modifying redox systems as well.

Long, H.C. de; Carlin, R.T. [Air Force Academy, CO (United States). Frank J. Seiler Research Lab.

1995-08-01T23:59:59.000Z

223

Ions on the Electrodeposition of Titanium in Molten Fluoride-chloride ...  

Science Conference Proceedings (OSTI)

Electrochemical Behavior of Calcium-Lead Alloys in Molten Salt Electrolytes ... on the Corrosion of Ni-Cased Alloys (NiCrW and NiCrMo) in Molten Fluorides.

224

CATALYTIC LIQUEFACTION BY ZINC CHLORIDE MELTS AT PRE-PYROLYSIS TEMPERATURE  

E-Print Network (OSTI)

blending and reaction conditions would be less than 10 centipoises, the effective viscosity of the melt/coal

Vermeulen, T.

2012-01-01T23:59:59.000Z

225

Pilot Evaluation of the Impact of Chloride on Selective Catalytic Reduction (SCR) Mercury Oxidation  

Science Conference Proceedings (OSTI)

This study investigated the effect of blending Powder River Basin (PRB) coal with an Eastern bituminous coal on the speciation of Hg across a selective catalytic reduction (SCR) catalyst. A pilot-scale coal combustor equipped with an SCR reactor for NOx control was used to evaluate the effect of coal blending on improving Hg oxidation across an SCR catalyst. Several parameters such as the ratio of PRB/bituminous coal blend and the concentrations of hydrogen halides (HCl, HBr, and HF) and halogens (Cl2 an...

2008-03-19T23:59:59.000Z

226

Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Racemic Secondary Allylic Chlorides with Alkylzincs  

E-Print Network (OSTI)

The transition metal-catalyzed enantioselective coupling of allylic electrophiles with carbon nucleophiles has been the focus of intense investigation.5 Salient examples include palladium-catalyzed couplings with enolates, ...

Fu, Gregory C.

227

HYDROGENOLYSIS OF A SUB-BITUMINOUS COAL WITH MOLTEN ZINC CHLORIDE SOLUTIONS  

E-Print Network (OSTI)

for Liquefaction and Gasification of Western Coals", in5272 (1976). COal Processing - Gasification, Liguefaction,or gaseous fuels, coal gasification has advanced furthest

Holten, R.R.

2010-01-01T23:59:59.000Z

228

COAL LIQUEFACTION USING ZINC CHLORIDE CATALYST IN AN EXTRACTING SOLVENT MEDIUM  

E-Print Network (OSTI)

Conference on Coal Gasification, Lique- faction, andInternational Symposium on Gasification and Liquefaction,coal, go to a gasification facility for conversion to

Gandhi, Shamim Ahmed

2013-01-01T23:59:59.000Z

229

HYDROGENOLYSIS OF A SUB-BITUMINOUS COAL WITH MOLTEN ZINC CHLORIDE SOLUTIONS  

E-Print Network (OSTI)

of char and gases. The Fischer-Tropsch process is an exampleprocess economics, the Fischer-Tropsch process has not beenevaluations for a Fischer-Tropsch plant in the United

Holten, R.R.

2010-01-01T23:59:59.000Z

230

COAL LIQUEFACTION USING ZINC CHLORIDE CATALYST IN AN EXTRACTING SOLVENT MEDIUM  

E-Print Network (OSTI)

volume of liquids. Fischer-Tropsch synthesis is an indirecthydrocarbons. The Fischer- Tropsch synthesis method produces

Gandhi, Shamim Ahmed

2013-01-01T23:59:59.000Z

231

EVIDENCE OF CORROSIVE GAS FORMED BY RADIOLYSIS OF CHLORIDE SALTS IN PLUTONIUM-BEARING MATERIALS  

SciTech Connect

Corrosion and pitting have been observed in headspace regions of stainless steel containers enclosing plutonium oxide/salt mixtures. These observations are consistent with the formation of a corrosive gas, probably HCl, and transport of that gas to the headspace regions of sealed containers. The NH{sub 4}Cl films found on the walls of the sealed containers is also indicative of the presence of HCl gas. Radiolysis of hydrated alkaline earth salts is the probable source of HCl.

Dunn, K.; Louthan, M.

2010-02-01T23:59:59.000Z

232

Low Temperature (T<100°C) Regeneration of HCl from the Chloride ...  

Science Conference Proceedings (OSTI)

Characterization of Indonesia Rare Earth Minerals and their Potential Processing Techniques · Characterization of Rare Earth Minerals with Field Emission ...

233

The Corrosion / Electrochemistry of Beryllium and Beryllium Weldments in Aqueous Chloride Environments  

E-Print Network (OSTI)

Oldani, LLNL Gary Devine, LLNL Janet Hauber, LLNL Bill Moddeman, PANTEX #12;ii Executive Summary The work

234

006- Does Addition of Fly Ash Decrease the Chloride Diffusivities of ...  

Science Conference Proceedings (OSTI)

085- Highly Efficient Comprehensive Utilization of Kaolin Tailings from ... 086- Improvement in Gas Tightness of YSZ Coatings Produced by Atmospheric Plasma Spraying ... 145- The Synergy of XRD and XRF in a Shale and Slate Analysis.

235

Recovery of Lead and Silver from Zinc Plant Residue by Chloride ...  

Science Conference Proceedings (OSTI)

Selective Recovery of Gold from E-wastes by Using Cellulosic Wastes · Stabilization of Chromium-Based Slags with FeS2 and FeSO4 · Sulphide Precipitation ...

236

Localized Plasticity in the Streamlined Genomes of Vinyl Chloride Respiring Dehalococcoides  

E-Print Network (OSTI)

Conceived and designed the experiments: PJM SFB FEL AMS.Performed the experiments: PJM SFB KMR.Analyzed the data: PJM SFB JAM JG KMR RW EG AL SH FEL AMS.

McMurdie, Paul J.

2010-01-01T23:59:59.000Z

237

Stereoconvergent Amine-Directed Alkyl–Alkyl Suzuki Reactions of Unactivated Secondary Alkyl Chlorides  

E-Print Network (OSTI)

A new family of stereoconvergent cross-couplings of unactivated secondary alkyl electrophiles has been developed, specifically, arylamine-directed alkyl–alkyl Suzuki reactions. This represents the first such investigation ...

Lu, Zhe

238

Spinning Carbon Fiber Precursors from 1-Butyl-3-Methylimidazolium Chloride Cellulose Solutions.  

E-Print Network (OSTI)

??Cellulose is an abundant natural renewable polymer that is used in the production of many materials. However, limited processibility and reduced solubility have restricted its… (more)

Gelderloos-Sammons, Rhea J

2007-01-01T23:59:59.000Z

239

ZINC CHLORIDE CATALYSIS IN COAL AND BIOMASS LIQUEFACTION AT PREPYROLYSIS TEMPERATURES  

E-Print Network (OSTI)

Howlett & A .. Gamache, Silviculture Biomass Farms; Vol. IV,a Potential Source of Biomass, Georgia Pacific Corp. MitreR.E. Inman, Silviculture Biomass Farms; Vol. 1 Summary,

Onu, Christopher O.

2013-01-01T23:59:59.000Z

240

HYDROGENOLYSIS OF A SUB-BITUMINOUS COAL WITH MOLTEN ZINC CHLORIDE SOLUTIONS  

E-Print Network (OSTI)

July 22, 1974. Project Western Coal: Conversion of Coal Intoand Gasification of Western Coals", in proceedings of ERDA/Investigators' Conference - Coal Research, Colorado School

Holten, R.R.

2010-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

COAL LIQUEFACTION USING ZINC CHLORIDE CATALYST IN AN EXTRACTING SOLVENT MEDIUM  

E-Print Network (OSTI)

iv List of Tables . , I. INTRODUCTION e o Coal Chemistry B.Coal Liquefaction c.Coal Liquefaction a D. II. o Experiment Equipment Summary of

Gandhi, Shamim Ahmed

2013-01-01T23:59:59.000Z

242

Development of Mercury and Hydrogen Chloride Emission Monitors for Coal Gasifiers  

SciTech Connect

The gas conditioning issues involved with coal gasification streams are very complex and do not have simple solutions. This is particularly true in view of the fact that the gas conditioning system must deal with tars, high moisture contents, and problems with NH{sub 3} without affecting low ppb levels of Hg, low levels (low ppm or less) of HCl, or the successful operation of conditioner components and analytical systems. Those issues are far from trivial. Trying to develop a non-chemical system for gas conditioning was very ambitious in view of the difficult sampling environment and unique problems associated with coal gasification streams. Although a great deal was learned regarding calibration, sample transport, instrumentation options, gas stream conditioning, and CEM design options, some challenging issues still remain. Sample transport is one area that is often not adequately considered. Because of the gas stream composition and elevated temperatures involved, special attention will need to be given to the choice of materials for the sample line and other plumbing components. When using gas stream oxidation, there will be sample transport regions under oxidizing as well as reducing conditions, and each of those regions will require different materials of construction for sample transport. The catalytic oxidation approach worked well for removal of tars and NH{sub 3} on a short term basis, but durability issues related to using the catalyst tube during extended testing periods still require study.

G. Norton; D. Eckels; C. Chriswell

2001-02-26T23:59:59.000Z

243

ZINC CHLORIDE CATALYSIS IN COAL AND BIOMASS LIQUEFACTION AT PREPYROLYSIS TEMPERATURES  

E-Print Network (OSTI)

of biomass utilization and conversion facilities. ChemicalChemical Structures of Biomass Components Chemical Liquefaction of Wood and l'lood Components Biomass Conversion

Onu, Christopher O.

2013-01-01T23:59:59.000Z

244

ORIGINAL PAPER Natural Fiber Reinforced Poly(vinyl chloride) Composites: Effect  

E-Print Network (OSTI)

, electric wires, window profiles, siding, etc. Recently, wood fiber reinforced PVC is getting more popular straw, rice husk, and pine fiber) and loading level of styrene-ethylene-butylene-styrene (SEBS) block copolymer on composite properties was investigated. Mechanical analysis showed that storage modulus

245

ZINC CHLORIDE CATALYSIS IN COAL AND BIOMASS LIQUEFACTION AT PREPYROLYSIS TEMPERATURES  

E-Print Network (OSTI)

pores of coal. c~n pene- Molten salts, particularly SnC1 2 ,the selection of ZnC1 2 as the molten salt catalyst for coalis very necessary. Molten salts have demonstrated catalytic

Onu, Christopher O.

2013-01-01T23:59:59.000Z

246

HYDROGENOLYSIS OF A SUB-BITUMINOUS COAL WITH MOLTEN ZINC CHLORIDE SOLUTIONS  

E-Print Network (OSTI)

Liquefaction Chemistry B. Molten Salt Catalysis RationaleUsed Equipment and Procedure Molten Salt a. b. c. Treat~entEquipment and Procedure Molten Salt Treatment a. Equipment

Holten, R.R.

2010-01-01T23:59:59.000Z

247

ZINC CHLORIDE CATALYSIS IN COAL AND BIOMASS LIQUEFACTION AT PREPYROLYSIS TEMPERATURES  

E-Print Network (OSTI)

Bodily, Stanford Res Inst. , Coal Chemistry Workshop, 1,News, (Aug. 27, 1979). C2 Coal Processing-Gasification,L.W. Vernon, and E.L. Wilson, Coal Liquefaction by the Exxon

Onu, Christopher O.

2013-01-01T23:59:59.000Z

248

Acetic Acid from the Carbonylation of Chloride Methane Over Rhodium Based Catalysts  

E-Print Network (OSTI)

on an indirect route via synthesis gas (syngas), i.e., methane is first con- verted to syngas before it is further transformed into other useful products [6]. However, the production of syngas from methane) 130:286­290 DOI 10.1007/s10562-009-0017-9 #12;[12], which is produced from syngas feedstock with Cu

Bao, Xinhe

249

Kinetics of solvolysis of 1-acectyl-4-(1-carboethoxy-1-cyano)methylene-1,4-dihydroquinoline in undried DMSO-d{sub 6} formation of acetic anhydride as an intermediate.  

SciTech Connect

The kinetics of solvolysis of the title compound (QAc) in undried DMSO-d{sub 6} to give 4-(1-ethoxycarbonyl-1-cyano)methylquinoline (QH) and HOAc at ambient temperature were investigated by {sup 1}H nmr spectrometry. With a limited excess of water the solvolysis follows a three-step process of QAc + H{sub 2}O{sup k1}{yields} QH + HOAC, and Ac{sub 2}O + H{sub 2}O{sup k3}{yields} 2HOA{sub c}, where k{sub 2} > k{sub 1} and k{sub 3} < k{sub 1}. Addition of pyridine-d5 to the reaction mixture markedly catalyzes the overall solvolysis, while addition of CF{sub 3}CO{sub 2}D to the reaction mixture simplifies the kinetics to pseudo first-order in [QAc] with k = 4.3 x 10{sup -3} min{sup -1}.

Klemm, L. H.; Lu, J. J.; Klemm, R. A.; Materials Science Division; Univ. of Oregon

1992-01-01T23:59:59.000Z

250

The development and evaluation of a sensitive minicolumn assay for the detection of aflatoxin M1 in milk  

E-Print Network (OSTI)

The aflatoxins comprise a subgroup of mycotoxins usually produced by Aspergillus parasiticus or Aspergillus flavus. Dairy cattle which ingest aflatoxin-contaminated feed will excrete aflatoxin M1 into the milk. The presence of this metabolite in milk is a concern for humans. At the present time, the best method to prevent ingestion of contaminated milk is by detection and diversion from our food supply. A field-practical method for the chemiselective immobilization and detection of aflatoxin M1 (CSID-M1) in milk has been developed in our laboratory. In this new method, aflatoxin M1 (AfM1) is selectively adsorbed in a small glass minicolumn at the interface of a layer of packed neutral sand and a narrow band of magnesium silicate (or Florisil). AfM1, at a level of 0.5 ppb or greater in contaminated milk, can be easily detected as a band of bright blue fluorescence with this assay. Briefly, whole milk- is diluted with water and passed through a C18 Sep-Pak cartridge. AfM1 is then partitioned by polarity and eluted from the cartridge with 2.5% acetone in methylene chloride. The eluate (containing AfM1) is added to the minicolumn detector. The tube is then washed with 2% methanol in methylene chloride and viewed under longwave UV light for AfM1. The limit o detection for CSID-M1 assay was determined to be 0.2 ppb compared with 0.3 ppb AfM1 using an immunoaffinity column extraction. The CSID-M1 assay was found to accurate, exhibiting no false positives or false negatives under the experimental condition imposed in this study. Also, the CSID-M1 detectors were shown to be chemically stable requiring no refrigeration for storage up to 20 weeks. In summary, the CSID-M1 assay was shown to be rapid, practical, easy to perform, and stable, thus facilitating its use in the prescreening of milk.

Cathey, Carol Grmela

1993-01-01T23:59:59.000Z

251

Experimental and theoretical investigation of the production of HCl and some metal chlorides in magmatic/hydrothermal systems  

DOE Green Energy (OSTI)

The theoretical analysis is given for calculating the composition of the aqueous vapor and the saline brine (hydrosaline liquid) present at run pressure and temperature in the experiment. The mixture of aqueous vapor and brine is homogenized upon quench. The method for calculating the concentration of HCl and NaCl in the coexisting aqueous vapor and brine is shown.

Not Available

1991-01-01T23:59:59.000Z

252

Atmospheric variability of methyl chloride during the last 300 years from an Antarctic ice core and firn air  

E-Print Network (OSTI)

as a low-pass filter, smoothing variations in the atmospheric composition of a gas over decadal time scales core measurements from Siple Dome provide evidence for a cyclic natural variability on the order of 10 increase measured in firn air may largely be a result of natural processes, which may continue to affect

Saltzman, Eric

253

Time-course analysis of the Shewanella amazonensis SB2B proteome in response to sodium chloride shock  

SciTech Connect

Organisms in the genus Shewanella have become models for response to environmental stress. One of the most important environmental stresses is change in osmolarity. In this study, we experimentally determine the response mechanisms of Shewanella amazonensis SB2B during osmotic stress. Osmotic stress in SB2B was induced through exposure to NaCl, and the time-course proteomics response was measured using liquid chromatography mass spectrometry. Protein trends were qualitatively compared to gene expression trends and to phenotypic characterization. Osmotic stress affects motility, and has also been associated with a change in the membrane fatty acid composition (due to induction of branched chain amino acid degradation pathways); however, we show this is not the case for SB2B. Although proteins and genes involved with branched chain amino acid degradation are induced, fatty acid degradation pathways are not induced and no change in the fatty acid profile occurs in SB2B as a result of osmotic shock. The most extensive response of SB2B over the time course of acclimation to high salt involves an orchestrated sequence of events comprising increased expression of signal transduction associated with motility and restricted cell division and DNA replication. After SB2B has switched to increased branched chain amino acid degradation, motility, and cellular replication proteins return to pre-perturbed levels.

Parnell, John J.; Callister, Stephen J.; Rompato, Giovanni; Nicora, Carrie D.; Pasa-Tolic, Ljiljana; Williamson, Ashley; Pfrender, Michael E.

2011-06-29T23:59:59.000Z

254

Experimental and theoretical investigation of the production of HCI and some metal chlorides in magmatic/hydrothermal systems  

DOE Green Energy (OSTI)

Progress in modifying a model in which the halogen (Cl and F) concentration in the mineral apatite in mid-crustal silicic plutonic systems can be used to make estimates of magmatic Cl and F concentrations at the time apatite was crystallizing is reviewed briefly. (MHR)

Piccoli, P.

1993-01-01T23:59:59.000Z

255

Regulation of the sodium/potassium/chloride cotransporter by calcium and cyclic AMP in cultured vascular smooth muscle cells  

SciTech Connect

The activity of the Na/K/Cl cotransporter in smooth muscle cells cultured from rat aorta was assayed by measuring the initial rate of furosemide-inhibitable /sup 86/Rb influx or efflux. Five uM furosemide or 0.2 uM bumetanide inhibited influx by 50%. Furosemide-inhibitable /sup 86/Rb influx depended on the presence of all 3 ions in the external medium. The dependence on Na and K was hyperbolic with apparent Km values of 45 and 5 mM, respectively. The dependence on Cl was sigmoidal. Assuming a stoichiometry of 1:1:2 for Na:K:Cl, a Km for Cl of 60 mM was obtained from a Hofstee plot of the data. Rapidly growing cells had 3 fold higher cotransport activity than quiescent cells. Angiotensin II (ANG) stimulated furosemide-inhibitable /sup 86/Rb efflux by 2 fold. An ANG receptor antagonist prevented ANG from increasing cotransport activity. Two calcium ionophores, A23187 and ionomycin, increased cotransport activity by 2 fold. Phorbol myristate acetate had no effect on cotransport activity. Isoproterenol, dibutyryl cyclic AMP, cholera toxin, or methylisobutylxanthine inhibited furosemide-sensitive /sup 86/Rb influx by 35 to 50%. From these findings they conclude that increasing cytoplasmic free calcium stimulates cotransport activity, whereas increasing cellular cyclic AMP inhibits the cotransporter.

Higgins, B.L.; Smith, L.; Smith, J.B.

1987-05-01T23:59:59.000Z

256

ZINC CHLORIDE-CATALYZED REACTIONS OF OXYGEN- AND SULFUR-CONTAINING COMPOUNDS WITH MODEL STRUCTURES IN COAL  

E-Print Network (OSTI)

H. H. , ed. , "Chemistry of Coal Utilization", Suppl. Vol. ,H. H. , ed. , "Chemistry of Coal Utilization", Suppl. Vol. ,Internat. Conf. Bituminous Coal, 3d Con£. , 2, 35 (1932);

Mobley, David Paul

2013-01-01T23:59:59.000Z

257

Impacts of Venturi Turbulent Mixing on the Size Distribution of Sodium Chloride and Dioctyl-Phthalate Aerosols  

DOE Green Energy (OSTI)

Internal combustion engines are a major source of airborne particulate matter (PM). The size of the engine PM is in the sub-micrometer range. The number of engine particles per unit volume is high, normally in the range of 10{sup 12} to 10{sup 14}. To measure the size distribution of the engine particles dilution of an aerosol sample is required. A diluter utilizing a venturi ejector mixing technique is commercially available and tested. The purpose of this investigation was to determine if turbulence created by the ejector in the mini-dilutor changes the size of particles passing through it.

Cheng, M.-D.; Wainman, T.; Storey, J.

2000-08-01T23:59:59.000Z

258

Impacts of Venturi Turbulent Mixing on the Size Distributions of Sodium Chloride and Dioctyl-Phthalate Aerosols  

DOE Green Energy (OSTI)

Internal combustion engines are a major source of airborne particulate matter (PM). The size of the engine PM is in the sub-micrometer range. The number of engine particles per unit volume is high, normally in the range of 10{sup 12} to 10{sup 14}. To measure the size distribution of the engine particles dilution of an aerosol sample is required. A diluter utilizing a venturi ejector mixing technique is commercially available and tested. The purpose of this investigation was to determine if turbulence created by the ejector in the mini-dilutor changes the size of particles passing through it. The results of the NaCl aerosol experiments show no discernible difference in the geometric mean diameter and geometric standard deviation of particles passing through the ejector. Similar results were found for the DOP particles. The ratio of the total number concentrations before and after the ejector indicates that a dilution ratio of approximately 20 applies equally for DOP and NaCl particles. This indicates the dilution capability of the ejector is not affected by the particle composition. The statistical analysis results of the first and second moments of a distribution indicate that the ejector may not change the major parameters (e.g., the geometric mean diameter and geometric standard deviation) characterizing the size distributions of NaCl and DOP particles. However, when the skewness was examined, it indicates that the ejector modifies the particle size distribution significantly. The ejector could change the skewness of the distribution in an unpredictable and inconsistent manner. Furthermore, when the variability of particle counts in individual size ranges as a result of the ejector is examined, one finds that the variability is greater for DOP particles in the size range of 40-150 nm than for NaCl particles in the size range of 30 to 350 nm. The numbers or particle counts in this size region are high enough that the Poisson counting errors are small (<10%) compared with the tail regions. This result shows that the ejector device could have a higher bin-to-bin counting uncertainty for ''soft'' particles such as DOP than for a solid dry particle like NaCl. The results suggest that it may be difficult to precisely characterize the size distribution of particles ejected from the mini-dilution system if the particle is not solid.

Cheng, M-D.

2000-08-23T23:59:59.000Z

259

Sorption of organic compounds in the aqueous phase onto tire rubber  

Science Conference Proceedings (OSTI)

Batch sorption tests were conducted to investigate the sorption capacity of organic compounds by ground tire and to assess the effects of the presence of other organic compounds, ionic strength, pH, ground tire particle size, and temperature on sorption. None of the factors were significant under the conditions tested, m-Xylene had the highest partition coefficient, followed by ethylbenzene, toluene, trichloroethylene, 1,1,1-trichloroethane, chloroform, and methylene chloride (13 L/kg). The partition coefficients had a logarithmic linear relationship with the octanol-water partition coefficients. The diffusion coefficients of the compounds tested were in the range of 10{sup {minus}8} cm{sup 2}/s. The diffusion coefficients did not correlate well with the physical/chemical properties, such as molecular size, of the compounds tested. The heat of solutions of the compounds tested had relatively low values. Thus, the sorption may not be affected significantly by temperature change. Organic compounds sorbed onto tire rubber appear to be sorbed primarily onto tire rubber polymeric materials and partially carbon black in the tire rubber. Overall, ground tire shows significant capacity as a sorbent of organic compounds.

Kim, J.Y.; Park, J.K.; Edil, T.B. [Univ. of Wisconsin, Madison, WI (United States). Dept. of Civil and Environmental Engineering

1997-09-01T23:59:59.000Z

260

Organic constituents in sour condensates from shale-oil and petroleum-crude runs at Sohio's Toledo refinery: identification and wastewater-control-technology considerations  

SciTech Connect

Samples of sour condensate generated from the continuous processing of both crude shale oil and petroleum crude were collected and extracted with methylene chloride. The extracts were analyzed using capillary-column gas chromatography/mass spectrometry at Argonne National Laboratory and Radian Corporation. Qualitatively, the predominant types of organic compounds present in the shale-oil sour condensate were pyridines and anilines; semiquantitatively, these compounds were present at a concentration of 5.7 ppM, or about 78% of the total concentration of components detected. In contrast, straight-chain alkanes were the predominant types of compounds found in the sour condensate produced during isocracking of conventional crude oil. The approximate concentration of straight-chain alkanes, 8.3 ppM, and of other branched and/or unsaturated hydrocarbons, 6.8 ppM, amounted to 88% of the total concentration of components detected in the sour condensate from the petroleum-crude run. Nitrogen compounds in the shale-oil sour condensate may necessitate alterations of the sour water and refinery wastewater-treatment facilities to provide for organics degradation and to accommodate the potentially greater ammonia loadings. This would include use of larger amounts of caustic to enhance ammonia removal by steam stripping. Possible problems associated with biological removal of organic-nitrogen compounds should be investigated in future experimental shale-oil refining runs.

Wingender, R J; Harrison, W; Raphaelian, L A

1981-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Organic constituents in process water from the in-situ retorting of oil from oil-shale kerogen  

SciTech Connect

Capillary-column gas-chromatography/mass-spectrometry (GC/MS) was performed on the acid, base, and neutral fractions of liquid- and particulate-phase methylene chloride extracts of a composite sample of raw process water collected from separator Tank 6 by the Laramie Energy Technology Center. Of the 160 extractable and chromatographable organic compounds tentatively identified, the following compound classes were found (listed in decreasing order of abundance): quinolines and lower fatty acids, aminoindoles, neutral oxygenated heterocyclics, pyridines, pyrroles, pyrazoles, phenols, and alkanes. Noticeably absent or in low concentration were alkyl benzenes and alkenes. Assuming 100% extraction efficiency, these organics constitute approximately 0.035% of the retort water; approximately 50% of this amount is represented by the quinolines, fatty acids, aminoindoles, and oxygenated heterocyclics. The following differences were noted in the composition of the particulate and liquid extracts of the neutral and base fractions, respectively: (1) alkanes are a major portion of the particulates, whereas oxygenated hereocyclics are most prominent in the liquid; and (2) aminoindoles are only a minor portion of the particulates, but are prominent in the liquid phase. The concentration of a compound occurring in both the liquid and particulate extracts is approximately 40 to 100 times higher in the liquid than in the particulate extract.

Raphaelian, L A; Harrison, W

1981-02-01T23:59:59.000Z

262

Solvent Extraction of Chemical Attribution Signature Compounds from Painted Wall Board: Final Report  

DOE Green Energy (OSTI)

This report summarizes work that developed a robust solvent extraction procedure for recovery of chemical attribution signature (CAS) compound dimethyl methyl phosphonate (DMMP) (as well as diethyl methyl phosphonate (DEMP), diethyl methyl phosphonothioate (DEMPT), and diisopropyl methyl phosphonate (DIMP)) from painted wall board (PWB), which was selected previously as the exposed media by the chemical attribution scientific working group (CASWG). An accelerated solvent extraction approach was examined to determine the most effective method of extraction from PWB. Three different solvent systems were examined, which varied in solvent strength and polarity (i.e., 1:1 dichloromethane : acetone,100% methanol, and 1% isopropanol in pentane) with a 1:1 methylene chloride : acetone mixture having the most robust and consistent extraction for four original target organophosphorus compounds. The optimum extraction solvent was determined based on the extraction efficiency of the target analytes from spiked painted wallboard as determined by gas chromatography x gas chromatography mass spectrometry (GCxGC-MS) analysis of the extract. An average extraction efficiency of approximately 60% was obtained for these four compounds. The extraction approach was further demonstrated by extracting and detecting the chemical impurities present in neat DMMP that was vapor-deposited onto painted wallboard tickets.

Wahl, Jon H.; Colburn, Heather A.

2009-10-29T23:59:59.000Z

263

Analysis of decontamination solutions of G agents to detect reformation of agent. Final report, December 1991-March 1992  

SciTech Connect

Agents from a full scale binary munition test were decontaminated with caustic in a 300 gal holding tank. Analysis of the contents by standard methods revealed a trace amount of G agent present despite the highly caustic solution. A technical review of the analytical methods was carried out to determine if the G agent was actually present or an artifact of the analysis. A literature search revealed similar concerns when brine solutions from nerve agent decontamination were analyzed using similar analytical methods. This study concluded that nerve agents reformed at reduced PH or in chloroform extracts of the neutralized or slightly acidic brines. Experiments using nuclear magnetic resonance (NMR), gas chromatography (GC), and GC/mass spectrometry (GC/MS) were used to see where, if any, G agent was present during the analysis. Results obtained confirmed G agent reforming in either the neutral aqueous solution or in the chloroform extract but not in chloroform extracts of the caustic solution. No agent was detected using methylene chloride as the extraction solvent as recommended by the earlier study.

Beaudry, W.T.; Buchanan, J.H.; Rohrbaugh, D.K.; Samuel, J.B.; Szafraniec, L.L.

1993-01-01T23:59:59.000Z

264

Ecological Interactions Between Metals and Microbes That Impact Bioremediation  

DOE Green Energy (OSTI)

Bacterial Community Diversity at a Mixed Waste Contaminated Site The correlation between bacterial population structure and lead, chromium and organic compounds present along a 21.6 m transect was examined. There was a gradient of heavy metal (Cr and Pb) and petroleum hydrocarbon contamination in these soils. A 16S rDNA analysis method and fatty acid methyl esters derived from phospholipids (PLFA) analysis were used to compare microbial communities. Soil microbial DNA was extracted and community fingerprint patterns for each sample location were produced by DGGE separation of the V3 region of the 16S rRNA genes amplified by PCR. Visual analysis of DGGE patterns indicated that sample locations with high concentrations of total toluene (12,000 mg kg-1), xylenes (8,000 mg kg-1), methylene chloride (10,000 mg kg-1), lead (17,000 mg kg-1) and chromium (3,200 mg kg-1) have a different community composition from the community with lower metals (200 mg kg-1) and organics (1200 mg kg-1) content. Microbial biomass, indicated by total phospholipid-P, was greatest in soils with highest organic contamination.

Konopka, Allan E.

2001-06-01T23:59:59.000Z

265

Technologic Papers 1922  

Science Conference Proceedings (OSTI)

... Thermal stresses in chilled iron car wheels, T 209, Burgess, GK ... Properties of electrical insulating materials of the laminated phenol-methylene type ...

2013-03-21T23:59:59.000Z

266

Chloride/magnesium ratio of shallow groundwaters as a regional geothermal indicator in Hawaii. Assessment of geothermal resources in Hawaii: Number 3  

DOE Green Energy (OSTI)

Because of the complex geological and hydrological conditions and the virtual lack of thermal springs, regional geothermal investigations in Hawaii require the use of techniques substantially different from those conventionally applied in other geothermal environments. The large number of hydrological wells in the state provides an appreciable source of groundwater chemical data. However, largely because of the island environment, interpretation of much of these data as geothermal indicators becomes ambiguous. Initially, SiO/sub 2/ and temperature of groundwaters were used to identify thermally anomalous zones, but on a regional basis it has been found that these criteria are not always successful. As a further criterion for assessment, the Cl/Mg ratio of the groundwater has been used. On a state-wide basis, this ratio has been successful in further screening the SiO/sub 2/-temperature selected sites, and in defining more specific areas which warrant further investigation. Temperature, SiO/sub 2/ and Cl/Mg values for nearly 400 groundwater samples are included.

Cox, M.E.; Thomas, D.M.

1979-11-01T23:59:59.000Z

267

Crystal structure of bis(isothiocyanato)[2,6-diacetylpyridine bis(4-hydroxybenzoylhydrazone)]Fe(III) Chloride bis(dimethylformamide) solvate  

SciTech Connect

The crystal structure of title compound (Fe[(C{sub 25}H{sub 21}N{sub 7}O{sub 4}S{sub 2})] {center_dot} 4(C{sub 3}NOH{sub 7}), where C{sub 3}NOH{sub 7} is dimethylformamide, DMF) was determined by the X-ray diffraction method. This compound crystallizes in the monoclinic C2/c space group, Z = 4. Unit cell parameters are: a = 13.6080(5), b = 17.6375(7), c = 19.5571(6) A, {beta} = 108.753(2) Degree-Sign . The N-H...O and O-H...O interactions stabilize the molecules in the lattice. The structure contains also the solvent dimethylformamide molecules, which are connected with intermoleculer hydrogen bond. The O atoms of DMF molecules take place as acceptor atoms.

Dilek, N., E-mail: nefised@gmail.com [Aksaray University, Department of Physics, Arts and Sciences Faculty (Turkey); Guenes, B. [Gazi University, Department of Physics Education, Gazi Education Faculty (Turkey)] [Gazi University, Department of Physics Education, Gazi Education Faculty (Turkey); Bueyuekguengoer, O. [Ondokuz Mayis University, Department of Physics, Arts and Sciences Faculty (Turkey)] [Ondokuz Mayis University, Department of Physics, Arts and Sciences Faculty (Turkey); Guep, R. [Mugla University, Department of Chemistry, Arts and Sciences Faculty (Turkey)] [Mugla University, Department of Chemistry, Arts and Sciences Faculty (Turkey)

2013-01-15T23:59:59.000Z

268

Comparison of phosgene, chlorine, and hydrogen chloride as reagents for converting molten CaO. CaCl/sub 2/ to CaCl/sub 2/  

Science Conference Proceedings (OSTI)

One method at Los Alamos for preparing impure plutonium metal from the impure oxide is by batch reduction with calcium metal at 850/sup 0/C in a CaCl/sub 2/ solvent. The solvent salt from this reduction is currently discarded as low-level radioactivity waste only because it is saturated with the CaO byproduct. We have demonstrated a pyrochemical technique for converting the CaO to CaCl/sub 2/ thereby incorporating solvent recycling into the batch reduction process. We will discuss the effectiveness of HCl, Cl/sub 2/, and COCl/sub 2/ as chlorinating agents and recycling actual spent process solvent salts. 6 refs., 8 figs.

Fife, K.W.

1985-01-01T23:59:59.000Z

269

Effect of secondary structure on the interactions of peptide T4 LYS (11-36) in mixtures of aqueous sodium chloride and 2,2,2,-Trifluoroethanol  

SciTech Connect

The potential of mean force for protein-protein interactions is key to the development of a statistical-mechanical model for salt-induced protein precipitation and crystallization, and for understanding certain disease states, including cataract formation and {beta}-amyloid pathology in Alzheimer's disease. Fluorescence anisotropy provides a method for quantitative characterization of intermolecular interactions due to reversible association. Monomer-dimer equilibria for the peptide T4 LYS(11-36) were studied by fluorescence anisotropy. This peptide, derived from the {beta}-sheet region of the T4 lysozyme molecule, has the potential to form amyloid fibrils. 2,2,2-trifluoroethanol (TFE) induces a change in peptide secondary structure, and was used in aqueous solutions at concentrations from 0 to 50% (v/v) at 25 and 37 C to examine the role of peptide conformation on peptide-peptide interactions. The association constant for dimerization increased with rising TFE concentration and with falling temperature. The peptide-peptide potential of mean force was computed from these association constants. Circular-dichroism measurements showed that the secondary structure of the peptide plays an important role in these strong attractive interactions due to intermolecular hydrogen-bond formation and hydrophobic interactions.

Anderson, Camille O.; Spiegelberg, Susanne; Prausnitz, John M.; Blanch, Harvey W.

2001-10-01T23:59:59.000Z

270

Structure of Hydronium (H3O+)/Chloride (Cl-) Contact Ion Pairs in Aqueous Hydrochloric Acid Solution: A Zundel-like Local Configuration  

SciTech Connect

Details of the H3O+ and H2O structure in the first solvation shell about Cl- in aqueous HCl solutions are reported from x-ray absorption fine structure (XAFS) measurements. Results show increasing degrees of contact ion pairing between Cl- and H3O+ as the HCl concentration increases from 6.0 m, 10.0 m and finally 16.1 m HCl (concentrated acid). At the highest acid concentration there are on average, approximately 1.6 H3O+ ions and 4.2 H2O’s in the first shell about Cl-. The structure of the Cl-/H3O+ contact ion pair is distinctly different than that of the H2O structure about Cl-. The Cl-O bond length (2.98Å) for Cl-/H3O+ is approximately 0.16 Å shorter than the Cl-/H2O bond. The bridging proton resides at an intermediate position between Cl and O at 1.60 Å from the Cl- and approximately 1.37 Å from the O of the H3O+. The bridging-proton structure of this contact ion pair, [Cl-H-OH2], is similar to structure of the water Zundel ion, [H2O-H-OH2]+. In both cases there is a shortened Cl-O or O-O bond and the intervening proton bond distances are substantially longer than for the covalent bonds of either HCl or H2O. The results further our understanding of the interaction H3O+ with Cl- that is of interest to fundamental physical chemistry and that has consequences in biochemical, geochemical and atmospheric processes.

Fulton, John L.; Balasubramanian, Mahalingam

2010-09-15T23:59:59.000Z

271

The Reaction Specificity of Nanoparticles in Solution: Application to the Reaction of Nanoparticulate Iron and Iron-Bimetallic Compounds with Chlorinated Hydrocarbons and Oxyanions  

SciTech Connect

The prospect for better remediation technologies using nanoparticles of iron, iron oxides, and iron with catalytic metals (i.e., bimetallics) has potentially transformative implications for environmental management of DOE sites across the country. Of particular interest is the potential to avoid undesirable products from the degradation of chlorinated solvents by taking advantage of the potential selectivity of nanoparticles to produce environmentally benign products from CCl{sub 4}. Chlorinated solvents are the most frequently reported subsurface contaminants across the whole DOE complex, and carbon tetrachloride (CCl{sub 4}) is the chlorinated solvent that is of greatest concern at Hanford (U. S. Department Energy 2001). In evaluating technologies that might be used at the site, a critical concern will be that CCl{sub 4} reduction usually occurs predominantly by hydrogenolysis to chloroform (CHCl{sub 3}) and methylene chloride (CH{sub 2}Cl{sub 2}), both of which are nearly as problematic as CCl{sub 4} (National Research Council, 1978). Competing reaction pathways produce the more desirable products carbon monoxide (CO) and/or formate (HCOO{sup -}), and possibly CO{sub 2}, but the proportion of reaction that occurs by these pathways is highly variable. Iron-based metallic and oxide nanoparticles have been shown to have enhanced reactivity towards a variety of chemical species, including chlorinated hydrocarbons and reducible oxyanions. Possibly of greater importance is the ability of nanoparticles to select for specific reaction products, potentially facilitating the formation of more environmentally acceptable products. The purpose of this study is to develop a fundamental understanding of the mechanism responsible for the overall particle reactivity and reaction selectivity of reactive metal and oxide nanoparticles. To achieve this objective the project involves the synthesis (using solution and vacuum synthesis methods) and characterization of well-defined nanoparticles, measurements of particle reactivity in solution or vacuum environments, and theory and modeling efforts to rationalize particle structure and reactivity.

None

2005-06-01T23:59:59.000Z

272

An analysis of tissues for total PCB and planar PCB concentrations in marine mammals stranded along the Gulf of Mexico  

E-Print Network (OSTI)

New methods developed in this study based upon extracting blubber by the maceration of the tissue in methylene chloride and subjecting the resulting extract to gel-permeation chromatography, provided a quick, reliable alternative to classical extraction and separation methods used for analysis of organochlorine residues in marine mammal tissues. Due to the lipophilic nature of PCBS, tissues high in lipid content, such as blubber and melon, give the best estimation of total body burden for the contaminants analyzed. Toxic Equivalents (TEQS) and baseline concentrations of total and planar PCBs in Atlantic bottlenose dolphins (Tursiops truncatus) which stranded along the Gulf of Mexico were determined in this study. The data suggests that concentrations of total PCBs and planar PCBs are not correlated, hence samples must be analyzed for both compounds in comprehensive studies. In the present study, PCB levels were statistically similar in 3 marine mammal species investigated (T. truncates, Stenella sp. , and Peponocephala electra). There appeared to be little correlation between PCB concentrations and stranding condition, stranding location or stranding year; however, a strong correlation was observed between the levels of PCBS, and the maturity and gender of the specimens analyzed. Male bottlenose dolphins accumulate PCBs throughout their lives as they mature, while females dolphins, once sexually mature, offload much of their body burdens of PCBs to their calves both transplacentally and through lactation. This trend would suggest that PCBs can be used as a chemical tracer in evaluating some biological and reproductive parameters of this species. Finally, preferential distribution of PCBs in different body blubber areas of T. truncatus was not observed in this study. This observation is possibly due to the homogeneous distribution of lipids in the thin blubber layer of these animals.

Davis, Joseph W.

1993-01-01T23:59:59.000Z

273

Water injection as a means for reducing non-condensible and corrosive gases in steam produced from vapor-dominated reservoirs  

E-Print Network (OSTI)

Chloride in Superheated Steam and Chloride in Deep Brine atGas and Chloride in Steam at The Geysers, Trans. , Geoth.Decline Trends in Geothermal Steam Reservoirs, Proceedings,

Pruess, Karsten; Spycher, Nicolas; Kneafsey, Timothy J.

2008-01-01T23:59:59.000Z

274

--No Title--  

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

Install additional injection wells in order to determine the most efficient delivery system for the silver chloride solution. F Area HWMF Silver Chloride Solution Injection Wells...

275

AOCS Official Method Da 9-48  

Science Conference Proceedings (OSTI)

Chlorides AOCS Official Method Da 9-48 Methods Methods and Analyses Analytical Chemistry Methods Downloads Methods Downloads DEFINITION This method determines the chlorides in the sample. SCOPE...

276

Index of Semiconductor Process Gases  

Science Conference Proceedings (OSTI)

... Hydrogen Bromide, HBr. Vinyl Fluoride. C 2 H 3 F. Hydrogen Chloride, HCl. Vinyl Chloride. C 2 H 3 Cl. Hydrogen Fluoride, HF. Trimethyl Gallium. ...

2012-07-27T23:59:59.000Z

277

AOCS Official Method S 4c-64  

Science Conference Proceedings (OSTI)

Methods for Testing Fatty Quaternary Ammonium Chlorides AOCS Official Method S 4c-64 Methods Downloads Methods Downloads DEFINITION   SCOPE Fatty quaternary ammonium chlorides a

278

PRODUCTION OF ELECTROLYTIC THORIUM CELL FEED BY A WET CHEMICAL METHOD. Process Report  

SciTech Connect

In order to produce a substantially oxide-free chloride. a specialized technique, based on the chemical characteristics of the ammonium thorium chloride complexes, has been found optimum. The procedure involves the formation of a solution of thorium chloride and ammonium chloride, evaporation of the solution to form a hydrated ammonium thorium chloride complex, dehydration of the complex by low-temperature drying, and ignition of the complex, after inter-mixture with an alkali chloride, to remove ammonium chloride and to form a thorium alkali chloride mixture for electrolysis. (L.T.W.)

Fisher, C.E.

1955-03-18T23:59:59.000Z

279

Compilation of NIST Higher-Order Methods for the ...  

Science Conference Proceedings (OSTI)

... Re-precipitate the chloride by drop-wise addition of nitric acid (10 % volume ... Load approximately 10 µg of chloride onto each of two rhenium side ...

2011-08-04T23:59:59.000Z

280

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 "75-09-2 methylene chloride" 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

TMS 2011: Proceedings and Publications  

Science Conference Proceedings (OSTI)

... Metals and Materials; Chloride 2011: Practice and Theory of Chloride-Based ... in Next Generation Nuclear Power Plants; Characterization of Nuclear Reactor ...

282

A new class of photoresponsive surfactants  

E-Print Network (OSTI)

In this thesis, a new class of nonionic, photoresponsive surfactants consisting of a polar di(ethylene oxide) head group attached to an alkyl spacer of between two and eight methylene groups, coupled through an ether linkage ...

Shang, Tiangang, 1969-

2005-01-01T23:59:59.000Z

283

Diffusion Coatings for Gas Turbine Engine Hot Section Parts  

Science Conference Proceedings (OSTI)

...ammonium chloride, and alumina was described in 1954 (Ref 12). Siliconizing of nickel and cobalt superalloys

284

What’s in Your Water?  

E-Print Network (OSTI)

vinyl chloride, and carbon dioxide under methanogenicof  nitrogen  and  carbon   dioxide,  to  maintain  an  

Polasko, Alexandra

2013-01-01T23:59:59.000Z

285

Chemical Hygiene and Safety Plan  

E-Print Network (OSTI)

pentafluoride bromine trifluoride carbonyl fluoride chlorinechlorine trifluoride cyanogen cyanogen chloride diboranetrifluoride carbonyl fluoride chlorine chlorine trifluoride

Ricks Editor, R.

2009-01-01T23:59:59.000Z

286

Technical Report Documentation Page 1. Report No.  

E-Print Network (OSTI)

Database (eGRID) #12;Page 2 A calcium chloride solution concentrates (regenerates) while passing over

Texas at Austin, University of

287

Humboldt National Forest East Mormon  

E-Print Network (OSTI)

Vegas Blue Diamond Paradise Trona Spring Valley Searles Valley Tonopah Chloride Searchlight Shoshone

Laughlin, Robert B.

288

Production of aluminum metal by electrolysis of aluminum sulfide  

DOE Patents (OSTI)

Production of metallic aluminum by the electrolysis of Al.sub.2 S.sub.3 at 700.degree.-800.degree. C. in a chloride melt composed of one or more alkali metal chlorides, and one or more alkaline earth metal chlorides and/or aluminum chloride to provide improved operating characteristics of the process.

Minh, Nguyen Q. (Woodridge, IL); Loutfy, Raouf O. (Tucson, AZ); Yao, Neng-Ping (Clarendon Hills, IL)

1984-01-01T23:59:59.000Z

289

Service Life Prediction  

Science Conference Proceedings (OSTI)

Prediction of Service Life of Reinforced Concrete Structure Exposed to Chlorides. Please supply the following parameters ...

2013-09-10T23:59:59.000Z

290

In-situ Analysis of Zinc Electrodeposition within an Ionic Liquid Electrolyte  

E-Print Network (OSTI)

chloride low temperature molten salt. Electrochimica Acta,room temperature molten salt. Journal of the Electrochemical

Keist, Jayme

2013-01-01T23:59:59.000Z

291

C1700098Cu-1.7Be-0.3Co  

Science Conference Proceedings (OSTI)

Table 30   Approximate corrosion resistance of C17000...Potassium sulfate Sodium hydroxide Picric acid Propane Sodium hypochlorite Potassium cyanide Rosin Sodium peroxide Silver chloride Sodium bicarbonate Sodium sulfide Sodium cyanide Sodium chloride Sulfur Stannic chloride Sodium sulfate Sulfur chloride Sulfuric acid, aerated Sulfur dioxide Sulfuric acid,...

292

C17200, C17300  

Science Conference Proceedings (OSTI)

Table 34   Approximate corrosion resistance of C17200 and C17300...Potassium hydroxide Phosphoric acid, aerated Propane Sodium hydroxide Picric acid Rosin Sodium hypochlorite Potassium cyanide Sodium bicarbonate Sodium peroxide Silver chloride Sodium chloride Sodium sulfide Sodium cyanide Sodium sulfate Sulfur Stannic chloride Sulfur dioxide Sulfur chloride Sulfuric...

293

Bacterial mutagenicity of polycyclic aromatic hydrocarbons in reconstituted mixtures and crude coal tar extracts and fractions  

E-Print Network (OSTI)

Although polycyclic aromatic hydrocarbons (PAHS) are one of the most ubiquitous carcinogens in the environment, little is known regarding their potential mutagenic interactions. Risk assessment of complex PAH mixtures utilizes toxic equivalency factors which assume additive interactions between individual PAHS. The mutagenic interactions of PAH mixtures were investigated using the Salmonellalmicrosome assay. Two groups of samples included PAH mixtures modeling a coal tar and an environmental crude coal tar extract and its fractions. The PAH mixtures were prepared in 2-, 3-, 4-ring and total reconstituted groups in the same percentages as a model coal tar. The environmental coal tar was extracted and separated into PAH fractions. Each sample was tested at 5 consecutive dose levels with and without metabolic activation in the Salmonella/microsome assay using tester strains TA98 and TAIOO. The reconstituted mixture elicited the maximum mutagenic response of 1,089 revertants at a dose of 1.8mg/mL. At the four lower dose levels (0.09mg/mL to 1.8mg/mL), the reconstituted induced a higher response than the 4-ring mixture. At the highest dose level (18mg/mL), the reconstituted showed a lower response that the 4-ring. These results suggest enhanced mutagenic responses at lower dose levels, with inhibition at higher doses. The mutagenicity of the PAH mixtures was evaluated in combinations as 2-:3-, 3-:4-, and 2-:4-ring mixtures. The 2-:4-ring, and 3-:4-ring combinations induced lower mutagenic responses than the 4-ring alone, suggesting inhibition by the 2-and 3-ring PAHS. Inhibition was also observed when benzo[a]pyrene was tested 935 net revertants, while the benzo[a]pyrene:reconstituted mixture induced 349 net revertants. The methylene chloride extract of a coal tar induced 385 net TA98 and 589 net TAIOO revertants with high metabolic activation (30%). Fractions from the coal tar extract and binary mixtures of individual chemicals with a reconstituted coal tar extract induced additive responses. These data indicate that mixtures of PAHs exhibit a variety of mutagenic interactions. The interactive responses appear controlled by concentration and metabolism of the PAHS. Research of this nature may aid in establishing a clearer understanding of risks and interactions which occur from exposure to PAHS.

Onufrock, Amy Mildred

1994-01-01T23:59:59.000Z

294

Catalytic activity of a series of Zn(II) phenoxides for the copolymerization of epoxides and carbon dioxide  

Science Conference Proceedings (OSTI)

A series of zinc phenoxides of the general formula (2,6-R{sub 2}C{sub 6}H{sub 3}O){sub 2}Zn(base){sub 2} [R = Ph, {sup t}Bu, {sup i}Pr, base = Et{sub 2}O, THF, or propylene carbonate] and (2,4,6-Me{sub 3}C{sub 6}H{sub 2}O){sub 2}Zn(pyridine){sub 2} have been synthesized and characterized in the solid state by X-ray crystallography. All complexes crystallized as four-coordinate monomers with highly distorted tetrahedral geometry about the zinc center. The angles between the two sterically encumbering phenoxide ligands were found to be significantly more obtuse than the corresponding angles between the two smaller neutral base ligands, having average values of 140{degree} and 95{degree}, respectively. In a noninteracting solvent such as benzene or methylene chloride at ambient temperature, the ancillary base ligands are extensively dissociated from the zinc center, with the degree of dissociation being dependent on the base as well as the substituents on the phenolate ligands. That is, stronger ligand binding was found in zinc centers containing electron-donating tert-butyl substituents as opposed to electron-withdrawing phenyl substituents. In all instances, the order of ligand binding was pyridine > THF > epoxides. These bis(phenoxide) derivatives of zinc were shown to be very effective catalysts for the copolymerization of cyclohexene oxide and CO{sub 2} in the absence of strongly coordinating solvents, to afford high-molecular-weight polycarbonate (M{sub w} ranging from 45 x 10{sup 3} to 173 x 10{sup 3} Da) with low levels of polyether linkages. However, under similar conditions, these zinc complexes only coupled propylene oxide and CO{sub 2} to produce cyclic propylene carbonate. Nevertheless, these bis(phenoxide) derivatives of zinc were competent at terpolymerization of cyclohexene oxide/propylene oxide/CO{sub 2} with little cyclic propylene carbonate formation at low propylene oxide loadings. While CO{sub 2} showed no reactivity with the sterically encumbered zinc bis(phenoxides), e.g., (2,6-di-tert-butylphenoxide){sub 2}Zn(pyridine){sub 2} to provide the corresponding aryl carbonate zinc derivative. At the same time, both sterically hindered and sterically nonhindered phenoxide derivatives of zinc served to ring-open epoxide, i.e., were effective catalysts for the homopolymerization of epoxide to polyethers. The relevance of these reactivity patterns to the initiation step of the copolymerization process involving these monomeric zinc complexes is discussed.

Darensbourg, D.J.; Holtcamp, M.W.; Struck, G.E.; Zimmer, M.S.; Niezgoda, S.A.; Rainey, P.; Robertson, J.B.; Draper, J.D.; Reibenspies, J.H.

1999-01-13T23:59:59.000Z

295

Transition-metal chromophore as a new, sensitive spectroscopic tag for proteins. Selective covalent labeling of histidine residues in cytochromes c with chloro(2,2':6',2''-terpyridine)platinum(II) chloride  

SciTech Connect

Reactivity and selectivity of Pt(trpy)Cl/sup +/ toward proteins are studied with cytochromes c from horse and tuna as examples. The new transition-metal reagent is specific for histidine residues at pH 5. The reaction, facile one-step displacement of the Cl/sup -/ ligand by imidazole, produces good yield. The binding sites, His 26 and His 33 in the horse protein and His 26 in the tuna protein, are identified by UV-vis spectrophotometry and by peptide-mapping experiments. Model complexes with imidazole, histidine, histidine derivatives, and histidine-containing peptides are prepared and characterized. The covalently attached Pt(trpy)/sup 2 +/ labels allow easy separation of the protein derivatives by cation-exchange chromatography. The labels do not perturb the conformation and reduction potential of cytochrome c, as shown by UV-vis spectrophotometry, cyclic voltammetry, differential-pulse voltammetry, EPR spectroscopy, and /sup 1/H NMR spectroscopy. The selectivity of Pt(trpy)Cl/sup +/ is entirely opposite from that of PtCl/sub 4//sup 2 -/ although both of them are platinum(II)-chloro complexes. Owing to an interplay between the steric and electronic effects of the terpyridyl ligand, the new reagent is unreactive toward methionine (a thio ether) and cystine (a disulfide), which are otherwise highly nucleophilic ligands, but very reactive toward imidazole, which is otherwise a relatively weak ligand. Unusual and useful selectivity of preformed transition-metal complexes toward proteins evidently can be achieved by a judicious choice of ancillary ligands.

Ratilla, E.M.A.; Brothers, H.M. II; Kostic, N.M.

1987-07-22T23:59:59.000Z

296

Mercury Measurements Characterizing the Impact of SCR on Mercury: Consol Test Site 3 - Eastern Bituminous Coal-Fired Power Plant Wit h an SCR, ESP, and Wet FGD; Impact of Chloride Addition  

Science Conference Proceedings (OSTI)

CONSOL Energy Inc., Research & Development (CONSOL), with support from the U.S. Department of Energy, National Energy Technology Laboratory (DOE) and the Electric Power Research Institute (EPRI), is evaluating the effects of selective catalytic reduction (SCR) on mercury (Hg) capture in coal-fired plants equipped with an electrostatic precipitator (ESP) - wet flue gas desulfurization (FGD) combination or a spray dyer absorber - fabric filter (SDA-FF) combination. In this program CONSOL is determining mer...

2006-04-26T23:59:59.000Z

297

PERFORMANCE OF LIQUI-CEL EXTRA-FLOW MEMBRANE CONTRACTOR IN A PURE WATER AND IN A 0.2% SODIUM CHLORIDE SOLUTION (SNO-STR-2001-11).  

SciTech Connect

After completion of SNO's first phase measurement of the neutrino charge current, two tons of salt were added into the SNO heavy water to increase the sensitivity of the neutral current measurement (Phase II). Liqui-Cel Extra-Flow Membrane Contactors (simply called Liqui-Cel) are used in the SNO heavy-water circulating system to remove the dissolved gases, such as oxygen, nitrogen, radon, and water vapor from the liquid water. One possible scenario with phase II operation is that the salt may leak through the Liqui-Cel Membrane and come in contact with the vacuum pumps and other metal components of the Heavy-Water Vapor Recovery System. In this scenario, corrosion will damage these components, especially the vacuum pump (Pfeiffer UniDry Pump with cast iron interior), and increase the operational difficulties. A series of tests for the behavior of the Liqui-Cel System in pure water and in salt systems was conducted at the Brookhaven National Laboratory in order to measure the transfer of (a) water vapor and (b) salt, if there is any, through the membrane. Initially a 10-inch by 28-inch Liqui-Cel unit, identical to those used in the SNO heavy-water circulating system, was obtained from SNO site. However, extensive analysis showed that the membrane in this unit was defective: a replacement membrane would cost several thousand dollars. Instead, a smaller, 2.5-inch x 8-inch Liqui-Cel, obtained from Dr. Richard Helmers of the University of British Columbia, was used in this experiment. A comparison of the present experiment with the SNO heavy-water system is done with theoretical calculations. The results are discussed in the following sections.

YEH,M.; BOGER,J.; HAHN,R.L.

2001-11-05T23:59:59.000Z

298

Determining the CH{sub 3}SO{sub 2}{yields}CH{sub 3}+SO{sub 2} barrier from methylsulfonyl chloride photodissociation at 193 nm using velocity map imaging  

Science Conference Proceedings (OSTI)

These imaging experiments study the formation of the methylsulfonyl radical, CH{sub 3}SO{sub 2}, from the photodissociation of CH{sub 3}SO{sub 2}Cl at 193 nm and determine the energetic barrier for the radical's subsequent dissociation to CH{sub 3}+SO{sub 2}. We first state-selectively detect the angular and recoil velocity distributions of the Cl({sup 2}P{sub 3/2}) and Cl({sup 2}P{sub 1/2}) atoms to further refine the distribution of internal energy partitioned to the momentum-matched CH{sub 3}SO{sub 2} radicals. The internal energy distribution of the radicals is bimodal, indicating that CH{sub 3}SO{sub 2} is formed in both the ground state and low-lying excited electronic states. All electronically excited CH{sub 3}SO{sub 2} radicals dissociate, while those formed in the ground electronic state have an internal energy distribution which spans the dissociation barrier to CH{sub 3}+SO{sub 2}. We detect the recoil velocities of the energetically stable methylsulfonyl radicals with 118 nm photoionization. Comparison of the total recoil translational energy distribution for all radicals to the distribution obtained from the detection of stable radicals yields an onset for dissociation at a translational energy of 70{+-}2 kcal/mol. This onset allows us to derive a CH{sub 3}SO{sub 2}{yields}CH{sub 3}+SO{sub 2} barrier height of 14{+-}2 kcal/mol; this determination relies on the S-Cl bond dissociation energy, taken here as the CCSD(T) predicted energy of 65.6 kcal/mol. With 118 nm photoionization, we also detect the velocity distribution of the CH{sub 3} radicals produced in this experiment. Using the velocity distributions of the SO{sub 2} products from the dissociation of CH{sub 3}SO{sub 2} to CH{sub 3}+SO{sub 2} presented in the following paper, we show that our fastest detected methyl radicals are not from these radical dissociation channels, but rather from a primary S-CH{sub 3} bond photofission channel in CH{sub 3}SO{sub 2}Cl. We also present critical points on the ground state potential energy surface of CH{sub 3}SO{sub 2} at the //CCSD(T)/aug-cc-pV(Q+d)ZCCSD(T)/6-311++G(2df,p) level. We include harmonic zero-point vibrational corrections as well as core-valence and scalar-relativistic corrections. The CCSD(T) predicted barrier of 14.6 kcal/mol for CH{sub 3}SO{sub 2}{yields}CH{sub 3}+SO{sub 2} agrees well with our experimental measurement. These results allow us to predict the unimolecular dissociation kinetics of CH{sub 3}SO{sub 2} radicals and critique the analysis of prior time-resolved photoionization studies on this system.

Ratliff, Britni J.; Tang Xiaonan; Butler, Laurie J. [Department of Chemistry and James Franck Institute, University of Chicago, Chicago, Illinois 60637 (United States); Szpunar, David E. [Department of Biological, Chemical, and Physical Sciences, Roosevelt University, Schaumburg, Illinois 60173 (United States); Lau, Kai-Chung [Department of Biology and Chemistry, City University of Hong Kong (Hong Kong)

2009-07-28T23:59:59.000Z

299

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 ...

300

Current Efficiency Predictive Model and Its Calibration and Validation  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Modelling  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

302

Latest Results from PFC Investigation in China  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

303

Anodic Electrochemical Behavior in Low Alumina Concentration ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

304

Electrolytic Cell Gas Cooling Upstream of Treatment Center  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

305

Current Distribution and Lorentz Field Modelling Using Cathode ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

306

Busbar Displacement Study of Aluminum Reduction Cell  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

307

DX+, An Optimized Version of DX Technology  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

308

Impacts of Anode Set on the Energy Re-distribution of PB Aluminum ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

309

Pot-Shell Exfoliation behind SiC Sidewall Block in a Cathode of ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

310

Numerical Simulation on Coupled Multi-field of the Perforated ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

311

Impurity Elements in Raw Gas Ultra-Fines from Aluminum ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

312

Specific Molecular Features of Potassium-Containing Cryolite Melts  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

313

Method for Testing Thermal Properties of Reduction Cell Materials  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

314

Visualising the Sources of Potroom Dust in Aluminium Smelters  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

315

Operating Parameters of Aluminum Electrolysis in a KF-AlF 3 Based ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

316

The Restart of Two Idled Pot Lines at Ormet Primary Aluminum  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

317

AP40  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

318

Prebake Potline Restart after Power Supply Interruption  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

319

About this Abstract  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

320

Building and Fire Publications  

Science Conference Proceedings (OSTI)

... Solar Energy Materials, Vol. ... Carino, NJ; Clifton, JR; Prototype Computer- Integrated Knowledge System: Predicting Service Life of Chloride-Exposed ...

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Electromagnetic and MHD Study to Improve Cell Performance of an ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

322

Air Amplified Boosted Suction (AABS) System for Pot Flow Control ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

323

Virtual Pot Simulator for aluminum smelting  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

324

Applying Nano Technology to Remove Toxic Sulfur Gases ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

325

Statistical Method to Predict Anode Effect Events  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

326

Two-Phase 3D Model of Reduction Cell  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

327

Thermo-Electro-Mechanical Investigation of Voltage Drop on Anode ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

328

CFD Simulation of Anode Bubble Behavior in Aluminum Reduction ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

329

Liquidus Temperatures of the System Na  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

330

The Study and Applications of Modern Potline Fume Treatment Plant ...  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

331

Behavior Estimation and Control of Aluminum Reduction Cell  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

332

Update on the Development of D18 Cell Technology at Dubal  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

333

Studies of Perfluorocarbon Formation on Anodes in Cryolite Melts  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

334

Optimization of the Thermal Management in Aluminum Smelting Pot  

Science Conference Proceedings (OSTI)

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride · Current Distribution and ...

335

DEVELOPMENTS IN AND IMPLEMENTATION OF GAS ...  

Science Conference Proceedings (OSTI)

... fire suppression mechanism (dilution, cooling, and strain ... oxidizers, such as potassium nitrate or potassium ... like coininon table salt, sodium chloride ...

2011-11-01T23:59:59.000Z

336

METHOD OF SEPARATING URANIUM VALUES, PLUTONIUM VALUES AND FISSION PRODUCTS BY CHLORINATION  

DOE Patents (OSTI)

The separation of plutonium and uranium from each other and from other substances is described. In general, the method comprises the steps of contacting the uranium with chlorine in the presence of a holdback material selected from the group consisting of lanthanum oxide and thorium oxide to form a uranium chloride higher than uranium tetrachloride, and thereafter heating the uranium chloride thus formed to a temperature at which the uranium chloride is volatilized off but below the volatilizalion temperature of plutonium chloride.

Brown, H.S.; Seaborg, G.T.

1959-02-24T23:59:59.000Z

337

Carbon Nanotubes Grown on Various Fibers - Oak Ridge National ...  

fiber materials inlcuding quartz wool fibers, carbon fibers, and activated carbon fibers. In each example a chloride solution of Fe, ...

338

NIST: Photon Cross Section Bibliography - Material List  

Science Conference Proceedings (OSTI)

... chloride Cadmium iodide Calcium carbonate Calcium fluoride Calcium hydride ... Freon 23) Triiodomethane Trimethyl benzene Uranium (IV) fluoride ...

339

JCODE FORMULA NAME ** JANAF INDEX SORTED BY ...  

Science Conference Proceedings (OSTI)

... 6 Al1Cl1(g) Aluminum chloride (AlCl) 74 1010 Al1Cl1+(g) Aluminum chloride, ion (AlCl+) 75 7 Al1Cl1F1(g) Aluminum chloride fluoride (AlClF) 76 ...

2013-03-22T23:59:59.000Z

340

PRODUCTION OF URANIUM TETRACHLORIDE  

DOE Patents (OSTI)

A process is descrlbed for the production of uranium tetrachloride by contacting uranlum values such as uranium hexafluoride, uranlum tetrafluoride, or uranium oxides with either aluminum chloride, boron chloride, or sodium alumlnum chloride under substantially anhydrous condltlons at such a temperature and pressure that the chlorldes are maintained in the molten form and until the uranium values are completely converted to uranlum tetrachloride.

Calkins, V.P.

1958-12-16T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

PROCESS OF DISSOLVING FUEL ELEMENTS OF NUCLEAR REACTORS  

DOE Patents (OSTI)

A process is described for dissolving stainless-steelor zirconium-clad uranium dioxide fuel elements by immersing the elements in molten lead chloride, adding copper, cuprous chloride, or cupric chloride as a catalyst and passing chlorine through the salt mixture. (AEC)

Wall, E.M.V.; Bauer, D.T.; Hahn, H.T.

1963-09-01T23:59:59.000Z

342

PRODUCTION OF PLUTONIUM METAL  

DOE Patents (OSTI)

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

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

1961-01-17T23:59:59.000Z

343

Calcination process for radioactive wastes  

DOE Patents (OSTI)

The present invention provides a method for minimizing the volatilization of chlorides during solidification in a fluidized-bed calciner of liquids containing sodium, nitrate and chloride ions. Zirconium and fluoride are introduced into the liquid, and one-half mole of calcium nitrate is added per mole of fluoride present in the liquid mixture. The mixture is calcined in the fluidized-bed calciner at about 500.degree.C., producing a high bulk density calcine product containing the chloride, thus tying up the chloride in the solid product and minimizing chloride volatilization.

Kilian, Douglas C. (Kennewick, WA)

1976-05-04T23:59:59.000Z

344

Feasibility of Detecting Byproducts of Chemical Weapons Manufacturing in Environmental Media: A Preliminary Evaluation  

DOE Green Energy (OSTI)

Quantitative information on the environmental transport and fate of organophosphorus nerve agents has been limited to studies conducted at high concentration representative of acute doses (Munroe et al. 1999). Nerve agents have relatively rapidly degradation rates at acute levels, and first order degradation pathways and half-lives have been characterized. However, similar knowledge is lacking in the open literature on the long-term environmental persistence of nerve agents, their manufacturing precursors and byproducts, and their degradation products, particularly at sub-acute or chronic health levels. Although many recent publications reflect low-level detection methods for chemical weapons signature compounds extracted from a variety of different media (e.g. D'Agostino et al., 2001; Kataoka et al., 2001), little of this work answers questions regarding their adsorptive character and chemical persistence. However, these questions are a central theme to both the detection of illegal chemical weapons manufacturing, as well as determining long-term cleanup needs and health risks associated with potential terrorist acts using such agents. Adsorption onto environmental surfaces can enhance the persistence of organophosphorus compounds, particularly with strong chelators like phosphonic acids. In particular, organophosphorus compound adsorption can lead to irreversible binding (e.g. Aubin and Smith, 1992), and current methods of chemical extraction and solid-state detection are challenged to detect them. This may be particularly true if the adsorbed compound is of a low initial concentration because it may be that the most preferred adsorption sites form the strongest bonds. This is particularly true in mixed media having various adsorption domains that adsorb at different rates (e.g. Weber and Huang, 1996). For high enough initial concentrations, sorption sites become saturated and solvent extraction has a relatively high efficiency. It is no surprise that many CW fate studies can report findings using traditional extraction or solid-state methods of detection, since release concentration exceed the capacity of environmental media to adsorb or degrade them. This report documents a test using solid-state {sup 31}P-NMR and GC/MS methods to delineate two adsorbed phosphonates on a uniform silica gel substrate at different concentrations. The test sought to determine the sensitivity of {sup 31}P-NMR detection, delineate adsorption character of the phosphonates, quantify their extraction efficiency using different solvents, and test the phosphonate mobility and photodegradability under short-term idealized conditions. The results show that solid-state detection at the experimental conditions can detect individual phosphonate species down to the 100 ppm level. Sensitivity could be further increased using larger samples and longer collection times. Solvent extraction of the phosphonates from the silica gel showed that a chlorinated solvent (methylene chloride) produced poor recovery for phosphonic acids from the silica gel, whereas methanol used as a solvent achieved high extraction efficiency. The phosphonates used showed strong aqueous mobility in a silica gel column experiment, with a small but significant amount left adsorbed to the substrate. A 96 hour photo-degradation experiment showed no degradation of the compounds.

Davisson, L; Reynolds, J G; Koester, C; Chinn, S C; Maxwell, R S; Love, A H; Viani, B E

2003-03-01T23:59:59.000Z

345

Elicitation of structure-specific antibodies by epitope scaffolds  

E-Print Network (OSTI)

Data Bank was searched for appropriate acceptor proteins (scaf- folds) with backbone structural and of protein chains with more than 50 residues. MAMMOTH (38) was used to search for sequence and structural consequences of changing a sulfur atom to a methylene group in the M13Nle mutation in ribonuclease

Baker, David

346

The Astrophysical Journal, 730:69 (10pp), 2011 April 1 doi:10.1088/0004-637X/730/2/69 C 2011. The American Astronomical Society. All rights reserved. Printed in the U.S.A.  

E-Print Network (OSTI)

Data Bank was searched for appropriate acceptor proteins (scaf- folds) with backbone structural and of protein chains with more than 50 residues. MAMMOTH (38) was used to search for sequence and structural consequences of changing a sulfur atom to a methylene group in the M13Nle mutation in ribonuclease

Kaiser, Ralf I.

347

Method for making carbon films  

DOE Patents (OSTI)

A method for treating an organic polymer material, preferably a vinylidene chloride/vinyl chloride copolymer (Saran) to produce a flat sheet of carbon film material having a high surface area ([approx equal]1000 m[sup 2] /g) suitable as an electrode material for super capacitor applications. The method comprises heating a vinylidene chloride/vinyl chloride copolymer film disposed between two spaced apart graphite or ceramic plates to a first temperature of about 160 C for about 14 hours to form a stabilized vinylidene chloride/vinyl chloride polymer film, thereafter heating the stabilized film to a second temperature of about 750 C in an inert atmosphere for about one hour to form a carbon film; and finally activating the carbon film to increase the surface area by heating the carbon film in an oxidizing atmosphere to a temperature of at least 750--850 C for between 1--6 hours. 2 figs.

Tan, M.X.

1999-07-29T23:59:59.000Z

348

Method for making carbon films  

DOE Patents (OSTI)

A method for treating an organic polymer material, preferably a vinylidene chloride/vinyl chloride copolymer (Saran) to produce a flat sheet of carbon film material having a high surface area (.apprxeq.1000 m.sup.2 /g) suitable as an electrode material for super capacitor applications. The method comprises heating a vinylidene chloride/vinyl chloride copolymer film disposed between two spaced apart graphite or ceramic plates to a first temperature of about 160.degree. C. for about 14 hours to form a stabilized vinylidene chloride/vinyl chloride polymer film, thereafter heating the stabilized film to a second temperature of about 750.degree. C. in an inert atmosphere for about one hour to form a carbon film; and finally activating the carbon film to increase the surface area by heating the carbon film in an oxidizing atmosphere to a temperature of at least 750-850.degree. C. for between 1-6 hours.

Tan, Ming X. (Livermore, CA)

1999-01-01T23:59:59.000Z

349

Carbon Film Electrodes For Super Capacitor Applications  

DOE Patents (OSTI)

A method for treating an organic polymer material, preferably a vinylidene chloride/vinyl chloride copolymer (Saran) to produce a flat sheet of carbon film material having a high surface area (.apprxeq.1000 m.sup.2 /g) suitable as an electrode material for super capacitor applications. The method comprises heating a vinylidene chloride/vinyl chloride copolymer film disposed between two spaced apart graphite or ceramic plates to a first temperature of about 160.degree. C. for about 14 hours to form a stabilized vinylidene chloride/vinyl chloride polymer film, thereafter heating the stabilized film to a second temperature of about 750.degree. C. in an inert atmosphere for about one hour to form a carbon film; and finally activating the carbon film to increase the surface area by heating the carbon film in an oxidizing atmosphere to a temperature of at least 750-850.degree. C. for between 1-6 hours.

Tan, Ming X. (Livermore, CA)

1999-07-20T23:59:59.000Z

350

Method of recycling lithium borate to lithium borohydride through methyl borate  

DOE Patents (OSTI)

This invention provides a method for the recycling of lithium borate to lithium borohydride which can be reacted with water to generate hydrogen for utilization as a fuel. The lithium borate by-product of the hydrogen generation reaction is reacted with hydrogen chloride and water to produce boric acid and lithium chloride. The boric acid and lithium chloride are converted to lithium borohydride through a methyl borate intermediate to complete the recycle scheme.

Filby, Evan E. (Rigby, ID)

1977-01-01T23:59:59.000Z

351

Method of recycling lithium borate to lithium borohydride through diborane  

DOE Patents (OSTI)

This invention provides a method for the recycling of lithium borate to lithium borohydride which can be reacted with water to generate hydrogen for utilization as a fuel. The lithium borate by-product of the hydrogen generation reaction is reacted with hydrogen chloride and water to produce boric acid and lithium chloride. The boric acid and lithium chloride are converted to lithium borohydride through a diborane intermediate to complete the recycle scheme.

Filby, Evan E. (Rigby, ID)

1976-01-01T23:59:59.000Z

352

Application of Oxygen Enrichment for the Pyrohydrolysis of Metal ...  

Science Conference Proceedings (OSTI)

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

353

Solvent Extraction for the Separation into Nickel and Cobalt with ...  

Science Conference Proceedings (OSTI)

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

354

EFFECTS OF LEWIS ACID CATALYSTS ON THE HYDROGENATION AND CRACKING OF TWO-RING AROMATIC AND HYDROAROMATIC STRUCTURES RELATED TO COAL  

E-Print Network (OSTI)

Using Zinc Chloride Catalysts in an Extracting Medium", LBL-EFFECTS OF LEWIS ACID CATALYSTS ON THE HYDROGENATION ANDEffects of Lewis Acid Catalysts on the Hydrogenation and

Salim, Sadie S.

2013-01-01T23:59:59.000Z

355

An Improved Non-Conventional Method for Obtaining Nuclear Pure ...  

Science Conference Proceedings (OSTI)

Aug 1, 2000 ... Uranium oxide (U3O8) is obtained from this precipitate by calcination for ... The latter is reduced by stannous chloride to obtain uranium trioxide ...

356

Failure of a Stainless Steel Braided Wire-reinforced Flexible Hose ...  

Science Conference Proceedings (OSTI)

Metallography revealed severe pitting and stress corrosion cracking (SCC). Cracking morphology changes from “lighting-bolt” typical of chloride stress corrosion ...

357

User Science Images  

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

but sodium and chloride being blocked. SlavaFull.png FES: Small Scale Experimental Plasma Research October 21, 2010 | Author(s): Vyacheslav Lukin (NRL) | Category: Fusion Energy |...

358

Oxygen-Consuming Chlor-Alkali Cell Configured To Minimize Peroxide...  

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

with the catalyst side away from the membrane, electrolysis of sodium chloride to chlorine and caustic (sodium hydroxide) proceeded with minimal peroxide formation. U.S. Patent...

359

THE PHOTOCHEMISTRY AND KINETICS OF GAS PHASE REACTIONS INVOLVING HO AND C1 RADICALS  

E-Print Network (OSTI)

Nitryl Chloride • • Chlorine Nitrate • • • • • • • • •emission from molecular chlorine resonance series excited byused in this work. Chlorine nitrate (ClON0 ) plays a major

Nelson, Herbert Hoffman

2013-01-01T23:59:59.000Z

360

SEPARATION OF PROTACTINIUM FROM CONTAMINANTS  

DOE Patents (OSTI)

The separation of protactinium by volatilization method is described. According to the invention, neutron irradiated finely divided thorium is reacted with aluminum trichloride or a mixture of aluminum trichloride and chlorine gas at a temperature of preferably between about 200 and 400 deg C. Following the chlorinating step the protactinium chloride along with aluminum chloride is selectively distilled from the mixture at a temperature of approximately 100 deg C. The protactinium chloride may be recovered from the mixture by treatment with sodium hydroxide, which converts the aluminum chloride to a soluble salt and forms insoluble protactinium hydroxide.

Malm, J.G.; Fried, S.

1959-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Page not found | Department of Energy  

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

Determination F Area Hazardous Waste Management Facility Silver Chloride Solution Injection Wells CX(s) Applied: B6.2 Date: 06152009 Location(s): Aiken, South Carolina...

362

CX-000496: Categorical Exclusion Determination | Department of...  

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

Determination F Area Hazardous Waste Management Facility Silver Chloride Solution Injection Wells CX(s) Applied: B6.2 Date: 06152009 Location(s): Aiken, South Carolina...

363

Categorical Exclusion Determinations: American Recovery and Reinvestme...  

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

Determination F Area Hazardous Waste Management Facility Silver Chloride Solution Injection Wells CX(s) Applied: B6.2 Date: 06152009 Location(s): Aiken, South Carolina...

364

Forensic Science  

Science Conference Proceedings (OSTI)

... has been developed.470 The application of Raman spectroscopy for the in situ detection of cocaine hydro- chloride in ... (24) Power, DA; Cordiner, SJ ...

2011-06-14T23:59:59.000Z

365

Journal of Research Volume 70A  

Science Conference Proceedings (OSTI)

... disk ampoule for anhydrous addition of hydrogen fluoride, p. 143 ... Thermodynamics of the ternary system: Water-calcium chloride-magnesium ...

2012-11-06T23:59:59.000Z

366

Bismuth generator method - Energy Innovation Portal  

Energy Innovation Portal ... The .sup.213 Bi is removed from the anion exchange resin by washing the anion exchange resin with a stripping solution free of chloride ...

367

Cryoscopic Data for Hall-Héroult Bath Containing Magnesium ...  

Science Conference Proceedings (OSTI)

Presentation Title, Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride. Author(s) ...

368

Cell Fundamentals, Phenomena and Alternatives II  

Science Conference Proceedings (OSTI)

Mar 14, 2012 ... Cryoscopic Data for Hall-Héroult Bath Containing Magnesium Fluoride, Calcium Fluoride, Potassium Cryolite, and Sodium Chloride: Asbjorn ...

369

The Equilibrium between Titanium Ions and Metal Titanium in ...  

Science Conference Proceedings (OSTI)

The electrochemical properties of titanium ions in fluoride-chloride were ... Electrochemical Behavior of Calcium-Bismuth Alloys in Molten Salt Electrolytes.

370

Session II - Programmaster.org  

Science Conference Proceedings (OSTI)

Mar 13, 2012 ... The electrochemical properties of titanium ions in fluoride-chloride were ... Electrochemical Behavior of Calcium-Bismuth Alloys in Molten Salt ...

371

Eliminating CO2 Emissions - Programmaster.org  

Science Conference Proceedings (OSTI)

TiO2 pigment is primarily produced by the high temperature chloride process, resulting in considerable CO2 emissions. A novel hydrometallurgical process for  ...

372

A New Production Route for Titanium Dioxide Pigment That ...  

Science Conference Proceedings (OSTI)

TiO2 pigment is primarily produced by the high temperature chloride process, resulting in considerable CO2 emissions. A new metallurgical process for making  ...

373

A New Production Route for Titanium Dioxide Pigment That ...  

Science Conference Proceedings (OSTI)

TiO2 pigment is primarily produced by the high temperature chloride process, resulting in considerable CO2 emissions. A novel hydrometallurgical process for  ...

374

Microsoft PowerPoint - Arkansa River System Operation.ppt  

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

Basin * 12 Section-7 lakes (owned by others) * 23 lakes with gated spillways * 8 COE Hydropower * 5 Navigation Locks * 1 Chloride Control Project Tulsa District: One Corps Serving...

375

FLUX COMPOSITION AND METHOD FOR TREATING URANIUM-CONTAINING METAL  

DOE Patents (OSTI)

A flux composition is preseated for use with molten uranium and uranium alloys. It consists of about 60% calcium fluoride, 30% calcium chloride and 10% uranium tetrafluoride.

Foote, F.

1958-08-26T23:59:59.000Z

376

Evaluation of Stress-Corrosion Cracking  

Science Conference Proceedings (OSTI)

Table 3   Stress-corrosion cracking of selected material systems...chlorides, seawater Oil/gas production and transmission, oil refining,

377

Hot Demonstrations of Nuclear-Waste Processing Technologies  

Science Conference Proceedings (OSTI)

The more chemically active fission products (alkali, alkaline earths, and rare earths) are oxidized as chlorides in the salt, while the more noble fission products

378

On the rough folding landscape of green fluorescent protein  

E-Print Network (OSTI)

aminomethane-hydrogen chloride WHAM Weighted histogramhistogram analysis method (WHAM) algorithm 110 was used towere analyzed using WHAM to determine statistics of

Andrews, Benjamin Thomas

2008-01-01T23:59:59.000Z

379

Microsoft PowerPoint - IPRC  

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

* Depleted uranium (III) chloride additions studied at INL Crushed salt in mason jar Desiccators 5 Electrochemistry Equipment - UW Electrochemistry glovebox Heater O 2...

380

The Bonding Structure of the Various High Purity or Binderless ...  

Science Conference Proceedings (OSTI)

... chloride (PVDC) at the condition of 5.5GPa and 1600°C. The PVDC became a supercritical fluid that will .... Tool Failure Criteria while Drilling Titanium Alloys.

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

EA-1157: Final Environmental Assessment | Department of Energy  

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

EA-1157: Final Environmental Assessment Methyl Chloride via Oxyhydrochlorination of Methane: A Building Black for Chemicals and Fuels from Natural Gas This EA evaluates the...

382

Crystal Structure of Iron-dependent Halogenase  

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

Iron (brown) is coordinated by two histidines, a-ketoglutarate (grey sticks), water (cyan), and chloride (green). The structural analysis revealed a novel coordination...

383

Reverse osmosis desalination and reclamation : control of colloidal and biofouling.  

E-Print Network (OSTI)

??The focus of this thesis work was on the fundamentals of colloidal and biofouling in reverse osmosis (RO) desalination and reclamation. A novel sodium chloride… (more)

Chong, Tzyy Haur.

2008-01-01T23:59:59.000Z

384

Modeling and Simulation of a Solar Assisted Desiccant Cooling...  

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

system comprises a desiccant wheel containing Lithium Chloride in tandem with a rotating heat exchanger and two humidifiers on both supply and return air. The required...

385

RADIOACTIVE HIGH LEVEL WASTE TANK PITTING PREDICTIONS: AN INVESTIGATION INTO CRITICAL SOLUTION CONCENTRATIONS  

Science Conference Proceedings (OSTI)

A series of cyclic potentiodynamic polarization tests was performed on samples of ASTM A537 carbon steel in support of a probability-based approach to evaluate the effect of chloride and sulfate on corrosion the steel?s susceptibility to pitting corrosion. Testing solutions were chosen to systemically evaluate the influence of the secondary aggressive species, chloride, and sulfate, in the nitrate based, high-level wastes. The results suggest that evaluating the combined effect of all aggressive species, nitrate, chloride, and sulfate, provides a consistent response for determining corrosion susceptibility. The results of this work emphasize the importance for not only nitrate concentration limits, but also chloride and sulfate concentration limits.

Hoffman, E.

2012-11-08T23:59:59.000Z

386

Prototype Cathode Processor (PCP) - Nuclear Engineering Division...  

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

processor has allowed the prototype unit to purify, by distillation, several hundred kilograms of uranium chloride salt produced by the Chemical Sciences and Engineering Division...

387

Integrated Plant to Recover Zinc, Lead and Silver from Crude Zinc ...  

Science Conference Proceedings (OSTI)

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

388

Tetrasubstituted Malonamide Derivatives and Hydrochloric Acid ...  

Science Conference Proceedings (OSTI)

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

389

Magnesium Removal from Secondary Aluminum Melts in ...  

Science Conference Proceedings (OSTI)

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

390

Segregation Roasting of a Saprolitic Laterite Ore: An Experimental ...  

Science Conference Proceedings (OSTI)

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

391

Plutonium Removal from Fluoride Spent Salts  

Science Conference Proceedings (OSTI)

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

392

Mechanism of Selective Chlorination of Reduced Limonitic Nickel ...  

Science Conference Proceedings (OSTI)

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

393

Precipitation of Hematite and Recovery of Hydrochloric Acid from ...  

Science Conference Proceedings (OSTI)

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

394

Zirconium Chlorination Behavior: A Literature Review  

Science Conference Proceedings (OSTI)

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

395

HCl Leaching and Acid Regeneration Using MgCl2 Brines and ...  

Science Conference Proceedings (OSTI)

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

396

Purification of Titanium Tetrachloride: A History  

Science Conference Proceedings (OSTI)

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

397

A Review of Recent Developments  

Science Conference Proceedings (OSTI)

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

398

About this Symposium  

Science Conference Proceedings (OSTI)

Aug 2, 2010 ... Recovery of Precious Metals from Chloride Media Using Microalgae Waste from Biofuel Extraction · Segregation Roasting of a Saprolitic ...

399

Investigation on the Corrosion Resistance of Several Steel Materials ...  

Science Conference Proceedings (OSTI)

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

400

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

Science Conference Proceedings (OSTI)

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

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

MT@TMS  

Science Conference Proceedings (OSTI)

Pyrohydrolysis, recycling of lixiviants, and water conservation will also be explored, as well as the potential use of chloride technology for the development of ...

402

NON-AQUEOUS DISSOLUTION OF MASSIVE PLUTONIUM  

DOE Patents (OSTI)

A method is presented for obtaining non-aqueous solutions or plutonium from massive forms of the metal. In the present invention massive plutonium is added to a salt melt consisting of 10 to 40 weight per cent of sodium chloride and the balance zinc chloride. The plutonium reacts at about 800 deg C with the zinc chloride to form a salt bath of plutonium trichloride, sodium chloride, and metallic zinc. The zinc is separated from the salt melt by forcing the molten mixture through a Pyrex filter.

Reavis, J.G.; Leary, J.A.; Walsh, K.A.

1959-05-12T23:59:59.000Z

403

About this Symposium  

Science Conference Proceedings (OSTI)

Aug 2, 2010... Study of Fluid Flow during Electrolytic Process for Magnesium Production ... Chloride Media Using Microalgae Waste from Biofuel Extraction.

404

Method of separating thorium from plutonium  

DOE Patents (OSTI)

A method of chemically separating plutonium from thorium. Plutonium and thorium to be separated are dissolved in an aqueous feed solution, preferably as the nitrate salts. The feed solution is acidified and sodium nitrite is added to the solution to adjust the valence of the plutonium to the +4 state. A chloride salt, preferably sodium chloride, is then added to the solution to induce formation of an anionic plutonium chloride complex. The anionic plutonium chloride complex and the thorium in solution are then separated by ion exchange on a strong base anion exchange column.

Clifton, David G. (Los Alamos, NM); Blum, Thomas W. (Los Alamos, NM)

1984-01-01T23:59:59.000Z

405

Method of separating thorium from plutonium  

DOE Patents (OSTI)

A method is described for chemically separating plutonium from thorium. Plutonium and thorium to be separated are dissolved in an aqueous feed solution, preferably as the nitrate salts. The feed solution is acidified and sodium nitrite is added to the solution to adjust the valence of the plutonium to the +4 state. A chloride salt, preferably sodium chloride, is then added to the solution to induce formation of an anionic plutonium chloride complex. The anionic plutonium chloride complex and the thorium in solution are then separated by ion exchange on a strong base anion exchange column.

Clifton, D.G.; Blum, T.W.

1984-07-10T23:59:59.000Z

406

98-3 Planning Report  

Science Conference Proceedings (OSTI)

... Chlorine reacts with the several contaminates of gold (copper, lead, nickel, zinc, cadmium, silver, etc.) to form a variety of chlorides (eg, copper ...

2012-10-16T23:59:59.000Z

407

Planar Power  

Science Conference Proceedings (OSTI)

Oct 12, 2010 ... A redesign of sodium-nickel chloride batteries promises to ... But, increasing operation temperature also shortens the battery's lifespan.

408

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 ...

409

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 ...

410

Effect of Cooling Rate on Gleeble Hot Ductility of UDIMET Alloy 720 ...  

Science Conference Proceedings (OSTI)

hydrofluoric acid, 30 ml sulfuric acid, 30 grams anhydrous iron chloride, 60 ml acetic acid, 300 ml water) was employed to reveal the ?' precipitates. In order to ...

411

Concrete Industry Benefits from Ancient Romans and the ALS  

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

the structure before it's immobilized. This process is important for the modern concrete industry because chloride corrosion of steel reinforcement is a major source of decay....

412

Concrete Industry Benefits from Ancient Romans and the ALS  

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

into the structure before it's immobilized. This process is important for the modern concrete industry because chloride corrosion of steel reinforcement is a major source of decay....

413

Furfuryl alcohol cellular product  

DOE Patents (OSTI)

Self-extinguishing rigid foam products are formed by polymerization of furfuryl alcohol in the presence of a lightweight, particulate, filler, zinc chloride and selected catalysts.

Sugama, T.; Kukacka, L.E.

1982-05-26T23:59:59.000Z

414

Research on Preparation and Properties of Inorganic Gelling ...  

Science Conference Proceedings (OSTI)

The experimental results show that the optimum process parameters are 1.0 kg desert sand, 0.24 L water glass solution, aluminum chloride solution with ...

415

--No Title--  

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

This activity involves the distillation of chloride, fluoride, and hydroxide salts under vacuum. A sample boat containing feed material will be placed into the salt distillation...

416

Y-12 continues to make changes in the 1970s  

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

biological decomposition of the raffinate 2 from solvent extraction and the distillation of nitric acid condensate coupled with the removal of flourides and chlorides was...

417

South Carolina | Department of Energy  

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

Office April 15, 2011 CX-005770: Categorical Exclusion Determination Vacuum Salt Distillation of Nonradioactive Chloride, Fluoride, and Hydroxide Salt CX(s) Applied: B3.6 Date:...

418

Impregnating magnetic components with MDA free epoxy  

Science Conference Proceedings (OSTI)

This paper describes the use of {open_quotes}Formula 456{close_quotes} an aliphatic amine cured epoxy for impregnating coils. Methylene dianiline (MDA) has been used for more than 20 years as the curing agent for various epoxy formulations throughout the Department of Energy. Sandia National Laboratories began the process of replacing MDA with other formulations because of regulations imposed by OSHA on the use of MDA.

Sanchez, R.O. [Sandia National Labs., Albuquerque, NM (United States); Domeier, L. [Sandia National Labs., Livermore, CA (United States); Gunewardena, S. [Mil-Spec Magnetics, Inc., Walnut, CA (United States)

1995-08-01T23:59:59.000Z

419

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

This invention describes a chemical process for desulfurizing coal, especially adaptable to the treatment of coal-water slurries, at temperatures as low as ambient, comprising treating the coal with aqueous titanous chloride whereby hydrogen sulfide is liberated and the desulfurized coal is separated with the conversion of titanous chloride to titanium oxides.

Slegeir, William A. (Hampton Bays, NY); Healy, Francis E. (Massapequa, NY); Sapienza, Richard S. (Shoreham, NY)

1985-01-01T23:59:59.000Z

420

Production of aluminum-26  

DOE Patents (OSTI)

This invention is a method of producing Al-26 from potassium chloride by exposing it to a proton beam in order to break potassium and chlorine atoms into smaller pieces, which include Al-26. The Al-26 is isolated from the potassium chloride and substances produced by the beam by means of extraction and ion exchange.

Steinkruger, F.J.; Phillips, D.R.

1990-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" 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

Plutonium recovery from spent reactor fuel by uranium displacement  

DOE Patents (OSTI)

A process for separating uranium values and transuranic values from fission products containing rare earth values when the values are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is reestablished.

Ackerman, John P. (Downers Grove, IL)

1992-01-01T23:59:59.000Z

422

New Mercury Control Technology for the Ft. Dix Waste-to-Energy Plant Sid Nelson Jr.  

E-Print Network (OSTI)

temperature. Mercury chloride (HgCI2) tends to be found in incinerator flue gases and this species may be well mercury measurement with no interference from acidic gases, such as S02. Low-Temperature Sorbents After of the oxidized mercury species, such as mercury chloride. Then, the large surface area in the baghouse would

Columbia University

423

1 Copyright 2010 by ASME Proceedings of the 18  

E-Print Network (OSTI)

temperature. Mercury chloride (HgCI2) tends to be found in incinerator flue gases and this species may be well mercury measurement with no interference from acidic gases, such as S02. Low-Temperature Sorbents After of the oxidized mercury species, such as mercury chloride. Then, the large surface area in the baghouse would

Columbia University

424

Universit de Droit, d'Economie et des Sciences d'Aix-Marseille (Aix-Marseille III)  

E-Print Network (OSTI)

temperature. Mercury chloride (HgCI2) tends to be found in incinerator flue gases and this species may be well mercury measurement with no interference from acidic gases, such as S02. Low-Temperature Sorbents After of the oxidized mercury species, such as mercury chloride. Then, the large surface area in the baghouse would

Paris-Sud XI, Université de

425

Plutonium recovery from spent reactor fuel by uranium displacement  

DOE Patents (OSTI)

This report discusses a process for separating uranium values and transuranic values from fission products containing rare earth values when the values which are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is re-established.

Ackerman, J.P.

1991-01-01T23:59:59.000Z

426

[Diffusion/dispersion transport of chemically reacting species]. Progress report, FY 1992--1993  

DOE Green Energy (OSTI)

Progress is reported on the following: calculation of activity coefficients for aqueous silica in alkali metal chloride solutions; calculation of degrees of formation of polyatomic clusters of Al in alkali chloride solutions; bulk composition-pH diagrams for arkosic sediments; and chemical interaction of petroleum, oil field brines, and authigenic mineral assemblages. Plans for future research are given.

Helgeson, H.C.

1993-07-01T23:59:59.000Z

427

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

428

Production of aluminum-26  

DOE Patents (OSTI)

A method of producing Al-26 from potassium chloride by exposing it to a proton beam in order to break potassium and chlorine atoms into smaller pieces, which include Al-26. The Al-26 is isolated from the potassium chloride and other substances produced by the beam by means of extraction and ion exchange.

Steinkruger, Fred J. (Los Alamos, NM); Phillips, Dennis R. (Los Alamos, NM)

1991-01-01T23:59:59.000Z

429

Development of a structure analysis algorithm on structures from CuCl2·2H2O crystallization with agricultural products  

Science Conference Proceedings (OSTI)

Crystallization patterns emerge when an aqueous dihydrate Copper chloride (CuCl"2@?2H"2O) solution in the presence of organic additives (juices/extracts) is crystallized on a glass plate. The emerging patterns are additive-specific and reflect physiological ... Keywords: Crystallization, Dihydrate Copper chloride, Food quality, GLCM, Physiological processes, ROI, Structure analysis, Texture analysis

Paul Doesburg; Andreas F. M. Nierop

2013-01-01T23:59:59.000Z

430

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

431

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

This invention describes a chemical process for desulfurizing coal, especially adaptable to the treatment of coal-water slurries, at temperatures as low as ambient, comprising treating the coal with aqueous titanous chloride whereby hydrogen sulfide is liberated and the desulfurized coal is separated with the conversion of titanous chloride to titanium oxides.

Slegeir, W.A.; Healy, F.E.; Sapienza, R.S.

1985-04-18T23:59:59.000Z

432

Study of anion adsorption at the gold--aqueous solution interface by atomic force microscopy  

SciTech Connect

The forces between a gold coated colloidal silica sphere and a pure gold plate have been measured in aqueous solution as a function of electrolyte concentration using an atomic force microscope (AFM). Forces in the presence of gold(III) chloride (HAuCl[sub 4]), sodium chloride, and trisodium citrate were recorded as a function of concentration. Each of these anion species is present during the formation of colloidal gold by the reduction of gold(III) chloride with trisodium citrate. In pure water the force between the gold surfaces was exclusively attractive. In sodium chloride or trisodium citrate solution a repulsive interaction was observed which is attributed to the adsorption of these anions at the gold/water interface. The observed interaction force in gold(III) chloride solution was always attractive, the surface potential never exceeding 20 mV. Data taken in aqueous solutions of citrate and chloride ions together suggested that the citrate ions were preferentially adsorbed to the surface of the gold. Addition of gold(III) chloride to the AFM liquid cell after the pre-adsorption of citrate anions caused the force of interaction to change from a repulsvie force to an attractive one initially as the gold(III) chloride was reduced to gold by the citrate anions. 33 refs., 11 figs.

Biggs, S.; Mulvaney, P.; Grieser, F. (Univ. of Melbourne (Australia)); Zukoski, C.F. (Univ. of Illinois, Urbana, IL (United States))

1994-10-05T23:59:59.000Z

433

Corrosion inhibition for distillation apparatus  

DOE Patents (OSTI)

Tower material corrosion in an atmospheric or sub-atmospheric distillation tower in a coal liquefaction process is reduced or eliminated by subjecting chloride-containing tray contents to an appropriate ion-exchange resin to remove chloride from such tray contents materials.

Baumert, Kenneth L. (Emmaus, PA); Sagues, Alberto A. (Lexington, KY); Davis, Burtron H. (Georgetown, KY); Schweighardt, Frank K. (Upper Macungie, PA)

1985-01-01T23:59:59.000Z

434

Volatility of HCl and the thermodynamics of brines during brine dryout  

DOE Green Energy (OSTI)

Laboratory measurements of liquid-vapor partitioning (volatility) of chlorides from brines to steam can be used to indicate the potential for corrosion problems in geothermal systems. Measurements of volatilities of solutes in chloride brines have established a possible mechanism for the production of high-chloride steam from slightly acidic high temperature brines. Questions concerning the fate of NaCl in the steam production process have been addressed through extensive measurements of its volatility from brines ranging in concentration from dilute solutions to halite saturation. Recent measurements of chloride partitioning to steam over brines in contact with Geysers rock samples are consistent with our concept of the process for production of high-chloride steam.

Simonson, J.M.; Palmer, D.A.

1997-04-01T23:59:59.000Z

435

Oxyhydrochlorination catalyst  

DOE Patents (OSTI)

An improved catalyst and method for the oxyhydrochlorination of methane is disclosed. The catalyst includes a pyrogenic porous support on which is layered as active material, cobalt chloride in major proportion, and minor proportions of an alkali metal chloride and of a rare earth chloride. On contact of the catalyst with a gas flow of methane, HCl and oxygen, more than 60% of the methane is converted and of that converted more than 40% occurs as monochloromethane. Advantageously, the monochloromethane can be used to produce gasoline boiling range hydrocarbons with the recycle of HCl for further reaction. This catalyst is also of value for the production of formic acid as are analogous catalysts with lead, silver or nickel chlorides substituted for the cobalt chloride.

Taylor, Charles E. (Pittsburgh, PA); Noceti, Richard P. (Pittsburgh, PA)

1992-01-01T23:59:59.000Z

436

Catalysts and method  

DOE Patents (OSTI)

An improved catlayst and method for the oxyhydrochlorination of methane is disclosed. The catalyst includes a pyrogenic porous support on which is layered as active material, cobalt chloride in major proportion, and minor proportions of an alkali metal chloride and of a rare earth chloride. On contact of the catalyst with a gas flow of methane, HC1 and oxygen, more than 60% of the methane is converted and of that converted more than 40% occurs as monochloromethane. Advantageously, the monochloromethane can be used to produce gasoline boiling range hydrocarbons with the recycle of HCl for further reaction. This catalyst is also of value for the production of formic acid as are analogous catalysts with lead, silver or nickel chlorides substituted for the cobalt chloride.

Taylor, Charles E. (Pittsburgh, PA); Noceti, Richard P. (Pittsburgh, PA)

1991-01-01T23:59:59.000Z

437

H.sub.2 /C.sub.12 fuel cells for power and HCl production - chemical cogeneration  

DOE Patents (OSTI)

A fuel cell for the electrolytic production of hydrogen chloride and the generation of electric energy from hydrogen and chlorine gas is disclosed. In typical application, the fuel cell operates from the hydrogen and chlorine gas generated by a chlorine electrolysis generator. The hydrogen chloride output is used to maintain acidity in the anode compartment of the electrolysis cells, and the electric energy provided from the fuel cell is used to power a portion of the electrolysis cells in the chlorine generator or for other chlorine generator electric demands. The fuel cell itself is typically formed by a passage for the flow of hydrogen chloride or hydrogen chloride and sodium chloride electrolyte between anode and cathode gas diffusion electrodes, the HCl increa This invention was made with Government support under Contract No. DE-AC02-86ER80366 with the Department of Energy and the United States Government has certain rights thereto.

Gelb, Alan H. (Boston, MA)

1991-01-01T23:59:59.000Z

438

H[sub 2]/Cl[sub 2] fuel cells for power and HCl production - chemical cogeneration  

DOE Patents (OSTI)

A fuel cell for the electrolytic production of hydrogen chloride and the generation of electric energy from hydrogen and chlorine gas is disclosed. In typical application, the fuel cell operates from the hydrogen and chlorine gas generated by a chlorine electrolysis generator. The hydrogen chloride output is used to maintain acidity in the anode compartment of the electrolysis cells, and the electric energy provided from the fuel cell is used to power a portion of the electrolysis cells in the chlorine generator or for other chlorine generator electric demands. The fuel cell itself is typically formed by a passage for the flow of hydrogen chloride or hydrogen chloride and sodium chloride electrolyte between anode and cathode gas diffusion electrodes. 3 figures.

Gelb, A.H.

1991-08-20T23:59:59.000Z

439

Dry halide method for separating the components of spent nuclear fuels  

DOE Patents (OSTI)

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

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

1998-01-01T23:59:59.000Z

440

Electrolytic process for preparing uranium metal  

SciTech Connect

An electrolytic process for making uranium from uranium oxide using Cl.sub.2 anode product from an electrolytic cell to react with UO.sub.2 to form uranium chlorides. The chlorides are used in low concentrations in a melt comprising fluorides and chlorides of potassium, sodium and barium in the electrolytic cell. The electrolysis produces Cl.sub.2 at the anode that reacts with UO.sub.2 in the feed reactor to form soluble UCl.sub.4, available for a continuous process in the electrolytic cell, rather than having insoluble UO.sub.2 fouling the cell.

Haas, Paul A. (Knoxville, TN)

1990-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

Method for locating metallic nitride inclusions in metallic alloy ingots  

DOE Patents (OSTI)

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

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

1992-01-01T23:59:59.000Z

442

A Preliminary Evaluation of Alternative Liquid Desiccants for a Hybrid Desiccant Air Conditioner  

E-Print Network (OSTI)

This paper presents the results of a preliminary investigation at The University of Texas at Austin of alternative liquid desiccants for use in a hybrid desiccant air-conditioning system in which a desiccant is circulated between the evaporator and the condenser of a vapor-compression air conditioner. The liquid desiccants studied were lithium chloride, lithium bromide, calcium chloride, and triethylene glycol. Each candidate desiccant was subjected to a screening process which weighed the merits of the desiccant in terms of selected characteristics. The best liquid desiccant for the anticipated application was found to be calcium chloride.

Studak, J. W.; Peterson, J. L.

1988-01-01T23:59:59.000Z

443

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

444

Process for converting light alkanes to higher hydrocarbons  

DOE Patents (OSTI)

A process is disclosed for the production of aromatic-rich, gasoline boiling range hydrocarbons from the lower alkanes, particularly from methane. The process is carried out in two stages. In the first, alkane is reacted with oxygen and hydrogen chloride over an oxyhydrochlorination catalyst such as copper chloride with minor proportions of potassium chloride and rare earth chloride. This produces an intermediate gaseous mixture containing water and chlorinated alkanes. The chlorinated alkanes are contacted with a crystalline aluminosilicate catalyst in the hydrogen or metal promoted form to produce gasoline range hydrocarbons with a high proportion of aromatics and a small percentage of light hydrocarbons (C.sub.2 -C.sub.4). The light hydrocarbons can be recycled for further processing over the oxyhydrochlorination catalyst.

Noceti, Richard P. (Pittsburgh, PA); Taylor, Charles E. (Pittsburgh, PA)

1988-01-01T23:59:59.000Z

445

Modelling the Hardening of Steel AISI 5115 by the Method Kuyucak  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

446

Effect of Dispersion by Carbon Dioxide on Secondary Alumina ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

447

Effects of Lime Additions on the Sulphur Distribution between Red ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

448

Microsoft PowerPoint - Proceedings Cover Sheets  

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

No. 10862,921) 2) Organo functional groups (U.S. Patent Application No. 10969,456) Organo acid chlorides (1); Organo chloroformates (2); Organo halides (3). R C Cl O O C...

449

--No Title--  

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

A silver chloride solution will be injected into the aquifer at the middle gate of the F-Area Barrier Wall, using CPT, for the treatment of I-129 in the groundwater plume. Silver...

450

Plasticizers Derived from Vegetable Oils  

This technology addresses the known health issues of commonly used petroleum-based plasticizers used in polyvinyl chloride (PVC), a high volume thermoplastic material (one that is moldable and formed by heating) by providing a biobased and renewable ...

451

Laboratory program to examine effects of layup conditions on pitting of Alloy 600. Final report. [PWR  

Science Conference Proceedings (OSTI)

The effect of various layup conditions on pitting of Alloy 600 tubing for steam generators was studied in beaker tests at 40/sup 0/C (104/sup 0/F). In addition, several methods to inhibit pitting were studied. The pitting solutions studied were copper chloride or seawater plus simulated sludge containing copper, copper oxide and magnetite. Results show that the pitting of Alloy 600 initiated in less than three weeks in the copper chloride solution with about 700 ppM chloride present. The same results were obtained in the seawater solution with about 6000 ppM chloride present. Retardation of pitting was achieved in three different ways: (1) decreasing the oxygen content of the solution, (2) decreasing the copper content of the solution, and (3) increasing the pH of the solution.

Whyte, D.D.

1983-04-01T23:59:59.000Z

452

U.S. Department of Energy Categorical Exclusion ...  

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

two batches of Reillex HPQ ion exchange resin in 786-A to prevent chloride stress corrosion cracking of stainless steel piping during HB-Line processing of MOX feed material....

453

URANIUM RECOVERY AND PURIFICATION PROCESS AND PRODUCTION OF HIGH PURITY URANIUM TETRAFLUORIDE  

DOE Patents (OSTI)

A process is described wherein an anionic exchange technique is employed to separate uramium from a large variety of impurities. Very efficient and economical purification of contamimated uranium can be achieved by treatment of the contaminated uranium to produce a solution containing a high concentration of chloride. Under these conditions the uranium exists as an aniomic chloride complex. Then the uranium chloride complex is adsorbed from the solution on an aniomic exchange resin, whereby a portion of the impurities remain in the solution and others are retained with the uramium by the resin. The adsorbed impurities are then removed by washing the resin with pure concentrated hydrochloric acid, after which operation the uranium is eluted with pure water yielding an acidic uranyl chloride solution of high purity.

Bailes, R.H.; Long, R.S.; Grinstead, R.R.

1957-09-17T23:59:59.000Z

454

Mesoporous titania nanocrystals by hydrothermal template growth  

Science Conference Proceedings (OSTI)

Mesoporous TiO2 nanocrystals have been synthetized by a classical sol-gel route integrated by an hydrothermal growth step using monomeric (dodecylpyridinium chloride, DPC) or dimeric gemini-like (GS3) surfactants as template directing agents. ...

Giuseppe Cappelletti; Silvia Ardizzone; Francesca Spadavecchia; Daniela Meroni; Iolanda Biraghi

2011-01-01T23:59:59.000Z

455

A METHOD FOR SEALING LITHIUM FLUORIDE WINDOWS TO PYREX VACUUM SYSTEMS  

SciTech Connect

A technique is described for sealing lithium fluoride windows to pyrex tubing using seals of silver chloride with intermediate siiver rings. Vacuum systems using these seals were satisfactory for several years. (J.R.D.)

Wildy, P.C.

1960-01-01T23:59:59.000Z

456

STATEMENT OF CONSIDERATIONS PETITION FOR ADVANCE WAIVER OF PATENT...  

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

synthesis and consolidation of cemented tungsten carbide (WC). The work is to produce nano-sized WC and Co powders from a vapor-phase mixture of chlorides of both WC and Co and...

457

Optimal estimation of the surface fluxes of chloromethanes using a 3-D global atmospheric chemical transport  

E-Print Network (OSTI)

The four chloromethanes - methyl chloride (CH3Cl), dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), are chlorine-containing gases contributing significantly to stratospheric ozone depletion ...

Xiao, Xue, Ph. D. Massachusetts Institute of Technology

2008-01-01T23:59:59.000Z

458

It's Elemental - The Element Strontium  

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

with potassium chloride (KCl), is then melted and electrolyzed, forming strontium and chlorine gas (Cl2). Most of the strontium produced today is used in the manufacture of color...

459

Manipulation of surface chemistry and nanostructure in porous silicon-based chemical sensors  

E-Print Network (OSTI)

Miskelly, G. M. The effect of chlorine and hydrogen chloride4.4.5 Exposure of Porous Si to Chlorine Gas……………………………..151after exposure to chlorine gas for 30 minutes………………………………….

Ruminski, Anne Marie

2009-01-01T23:59:59.000Z

460

The Evolution of Sustainable Personal Vehicles  

E-Print Network (OSTI)

and a pluggable lithium-ion battery pack capable ofbattery for all BEV, nickel metal hydride and lithium-ionlithium-ion & lithium polymer, and sodium nickel metal chloride. Each of these battery

Jungers, Bryan D

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "75-09-2 methylene chloride" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

Speciality conference on: toxic substances in the air environment  

SciTech Connect

Papers presented are divided into the following categories: toxic substances legislation; arsenic; vinyl chloride; and emerging problems in toxic emission. Seven papers were abstracted and indexed individually for ERA/EDB. (JGB)

1977-01-01T23:59:59.000Z

462

The Relationship between Particulate Chemistry and Air Masses in Southern Indiana  

Science Conference Proceedings (OSTI)

The particulate characteristics of the surface layer of the atmosphere over a region of southwest Indiana were determined for forty-two 24-hour periods between September 1985 and April 1986. The water-soluble sulfate, chloride and sodium content ...

Richard H. Grant; William W. McFee

1989-03-01T23:59:59.000Z

463

Statistical Analysis of Precipitation Chemistry Measurements over the Eastern United States. Part III: The Ionic Balance among Chemical Constituents  

Science Conference Proceedings (OSTI)

The relationships between acidity and the principal chemical constituents of precipitation (including sulfate, nitrate, ammonium, calcium, magnesium, sodium, and chloride) were investigated using a new archive of daily precipitation chemistry ...

Ronald J. Ferek; Barrett P. Eynon; Roy M. Endlich

1988-12-01T23:59:59.000Z

464

SANDIA REPORT SAND964839 UC-400 Unlimited Release  

Office of Scientific and Technical Information (OSTI)

relevance. Although the Li - thionyl chloride system yields high open circuit voltage and energy density, it has start-up problems after storage (i.e. voltage-delay), shows...

465

Chemical Resistance Chart  

Science Conference Proceedings (OSTI)

... 0. 53. Ethylene Oxide, 21, 4, 17, 5, 1, 5, 1, 5, 189, 2, 48, 4. 54. Hydrogen Fluoride, 210, 2, 1, 5, 142, 1, 1, 5, ND, 0, 6, 3. 55. Methyl Chloride, ...

466

AOCS Official Method Tn 2a-86  

Science Conference Proceedings (OSTI)

Flash Point of Fatty Quaternary Ammonium Chloride, Closed Cup Method (Modified Closed Cup Method, ASTM Designation D 93-80) AOCS Official Method Tn 2a-86 Methods Downloads Methods Downloads DEFINITION This method

467

AOCS Official Method Tg 3a-64  

Science Conference Proceedings (OSTI)

Iodine Value of Fatty Quaternary Ammonium Chlorides, Modified Wijs Method AOCS Official Method Tg 3a-64 Methods Downloads Methods Downloads DEFINITION The iodine value is a measure of the unsaturation of the alkyl

468

AOCS Official Method Tu 1a-64  

Science Conference Proceedings (OSTI)

pH of Fatty Quaternary Ammonium Chlorides AOCS Official Method Tu 1a-64 Methods Downloads Methods Downloads DEFINITION This method determines the pH of the test sample in water under the conditions of the test....

469

AOCS Official Method Te 3a-64  

Science Conference Proceedings (OSTI)

Acid Value and Free Amine Value of Fatty Quaternary Ammonium Chlorides AOCS Official Method Te 3a-64 Methods Downloads Methods Downloads DEFINITION The acid value is the mg of potassium hydroxide necessary to neut

470

AOCS Official Method Tv 1a-64  

Science Conference Proceedings (OSTI)

Average Molecular Weight of Fatty, Quaternary Ammonium Chlorides AOCS Official Method Tv 1a-64 Methods Downloads Methods Downloads DEFINITION This method determines the average molecular weight of a fatty quaterna

471

Characterization of Freckles in a High Strength Wrought Nickel ...  

Science Conference Proceedings (OSTI)

dissolved gases, the reduction of oxide inclusions, minimization of detrimental trace .... in alloys having high titanium/aluminum ratios, and it typically precipitates in a .... (anhydrous ferric chloride, nitric, and hydrochloric acids). Additionally ...

472

PREPARATION OF URANIUM MONOSULFIDE  

DOE Patents (OSTI)

A process is given for preparing uranium monosulfide from uranium tetrafluoride dissolved in molten alkali metal chloride. A hydrogen-hydrogen sulfide gas mixture passed through the solution precipitates uranium monosulfide. (AEC)

Yoshioka, K.

1964-01-28T23:59:59.000Z

473

Advances in the Stille reaction and new methods for continuous flow Pd-catalyzed C-N bond forming reactions  

E-Print Network (OSTI)

Chapter 1: A highly active catalyst system based upon a biaryl monophosphine ligand, XPhos, for the palladium-catalyzed Stille reaction has been developed. This method allows for the coupling of aryl chlorides with a range ...

Naber, John R. (John Robert)

2010-01-01T23:59:59.000Z

474

JCODE FORMULA NAME ** JANAF INDEX SORTED BY ...  

Science Conference Proceedings (OSTI)

... 695 1090 Ca1Cl2(g) Calcium chloride (CaCl2) 696 1056 Ca1F1(g) Calcium fluoride (CaF) 697 1057 Ca1F2(cr) Calcium fluoride (CaF2) 698 1058 ...

2013-03-22T23:59:59.000Z

475

Summary - Mitigation and Remediation of Mercury Contamination...  

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

and stakeholders. 2. "Quick Wins" were recommended for near term improvements as follows: Outfall 200- (a) use of stannous chloride in the NS Pipe to volatilize Hg, (b) addition of...

476

Direct Electroreduction of Oxides in Molten Fluorides  

Science Conference Proceedings (OSTI)

However, up to now, the use of chloride salts is still problematic partially because ... Electrochemical Reduction of Tantalum Oxide in a CaCl2 – CaO Molten Salt ...

477

Hot Dip Aluminum-Zinc Coatings  

Science Conference Proceedings (OSTI)

...Soil number Description pH Resistivity, Ω · cm 1 Native shale, clay: wet to dry 4 76,000 2 Native shale with chloride and sulfate salts: wet

478

Effects of Anthracite on Pelletization of Hematite Ore  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

479

Production of Fe-Based Alloys by Metallothermic Reduction of Mill ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

480

Study on Double-Layered Pellet Roasting of Sulfur & Arsenic ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

Note: This page contains sample records for the topic "75-09-2 methylene chloride" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


481

Research on the Influence of Moulding Sand with Furan Resin on ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

482

Production of Molybdenum Containing Iron Based Alloys via ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

483

Study on Apprasial Model of Iron Ores Based on Multi-level Fuzzy ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

484

Comprehensive Effect of Coke Breeze and Limestone Particle Size ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

485

Optimizing the Sintering Process of Low-Grade Ferromanganese Ores  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

486

Study for Influence of Prereduction Degrees on the Softening and ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

487

Reduction and Separation of High Iron Content Manganese Ore and ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

488

Study on the Magnetic Roasting Kinetic of Oolitic Hematite  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

489

The Directional Preparation of Colored Steel Slag Glass-ceramic  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

490

Research on Inclusions in CuCr Alloy Prepared by Thermit Reduction  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

491

Co-Cr-Mo Alloys Production by Self Propagating High Temperature ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

492

Sintering Process of Chromite Concentrate  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

493

Mechanisms of Iron and Slag Separation in Carbon Composite Iron ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

494

Tensile Mechanical Properties and Brittle Effect of Austempered Cr ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

495

Effects of Crystallization of Mould Fluxes on Property of Liquid Slag ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

496

CFD Model Development for Gaseous Reduction of Iron Ore Fines ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

497

Comparative Study on the Metal Aluminum Produced from Alumina ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

498

Effect of Reduction Conditons on Pre-reduction Behaviors of Self ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

499

Study on Improving the Strength of Copper Concentrate Pellets by ...  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.

500

Direct Redaction of TI-V Magnetite Via ITmk3 Technology  

Science Conference Proceedings (OSTI)

Chemical Enrichment of Precious Metals in Iron Sulfides Using Microwave Energy · Chloridizing ... Co-Gasification Behavior of Metallurgical Coke with High and Low Reactivity .... Thermal Plasma Torches for Metallurgical Applications.