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Note: This page contains sample records for the topic "heavy metals removal" 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
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1

Process for removing heavy metal compounds from heavy crude oil  

DOE Patents (OSTI)

A process is provided for removing heavy metal compounds from heavy crude oil by mixing the heavy crude oil with tar sand; preheating the mixture to a temperature of about 650.degree. F.; heating said mixture to up to 800.degree. F.; and separating tar sand from the light oils formed during said heating. The heavy metals removed from the heavy oils can be recovered from the spent sand for other uses.

Cha, Chang Y. (Golden, CO); Boysen, John E. (Laramie, WY); Branthaver, Jan F. (Laramie, WY)

1991-01-01T23:59:59.000Z

2

Magnetic Process For Removing Heavy Metals From Water Employing Magnetites  

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

Magnetic Process For Removing Heavy Metals From Water Employing Magnetic Process For Removing Heavy Metals From Water Employing Magnetites Magnetic Process For Removing Heavy Metals From Water Employing Magnetites A process for removing heavy metals from water is provided. The process includes the steps of introducing magnetite to a quantity of water containing heavy metal. Available for thumbnail of Feynman Center (505) 665-9090 Email Magnetic Process For Removing Heavy Metals From Water Employing Magnetites A process for removing heavy metals from water is provided. The process includes the steps of introducing magnetite to a quantity of water containing heavy metal. The magnetite is mixed with the water such that at least a portion of, and preferably the majority of, the heavy metal in the water is bound to the magnetite. Once this occurs the magnetite and

3

Using Microwave Radiation for Removing Heavy Metal Ions and ...  

Science Conference Proceedings (OSTI)

Presentation Title, Using Microwave Radiation for Removing Heavy Metal Ions and Producing Biofuels. Author(s), Aharon Gedanken. On-Site Speaker (Planned ) ...

4

SEPARATION OF HEAVY METALS: REMOVAL FROM INDUSTRIAL WASTEWATERS  

Office of Scientific and Technical Information (OSTI)

SEPARATION SEPARATION OF HEAVY METALS: REMOVAL FROM INDUSTRIAL WASTEWATERS AND CONTAMINATED SOIL* Robert W. Peters + and Linda Shem Energy Systems Division Argonne National Laboratory 9700 South Cass Avenue Argonne, Illinois 60439 Abstract This paper reviews the applicable separation technologies relating to removal of heavy metals from solution and from soils in order to present the state-of-the-art in the field. Each technology is briefly described and typical operating conditions and technology performance are presented. Technologies described include chemical precipitation (including hydroxide, carbonate, or sulfide reagents), coagulation/flocculation, ion exchange, solvent extraction, extraction with chelating agents, complexation, electrochemical operation, cementation, membrane operations, evaporation, adsorption, solidification/stabilization, and

5

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

SciTech Connect

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

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

1994-02-01T23:59:59.000Z

6

Literature review on the use of bioaccumulation for heavy metal removal and recovery. Volume 2  

Science Conference Proceedings (OSTI)

Bioaccumulation of metals by microbes -- `` bioremoval`` -- is a powerful new technology for the concentration, recovery, and removal of toxic heavy metals and radionuclides from waste streams and contaminated environments. Algae are particularly well suited for metal bioremoval. A recent commercial application of bioremoval utilizes inert (dead) immobilized microalgae biomass as ion exchange materials for the removal of heavy metals from industrial waste waters. Also, living microalgal cultures have been used to remove metals from mine effluents. Microbial cells and biomass can bioaccumulate metals and radionuclides by a large variety of mechanisms, both dependent and independent of cell metabolism. Microbial cell walls can act as ion exchange and metal complexation agents. Heavy metals can precipitate and even crystallize on cell surfaces. Metabolically produced hydrogen sulfide or other metabolic products can bioprecipitate heavy metals. Many microbes produce both intra- and extracellular metal complexing agents which could be considered in practical metal removal processes. Bioremoval processes are greatly affected by the microbial species and even strain used, pH, redox potential, temperature, and other conditions under which the microbes are grown. Development of practical applications of bioremoval requires applies research using the particular waste solutions to be treated, or close simulations thereof. From a practical perspective, the selection of the microbial biomass and the process for contacting the microbial biomass with the metal containing solutions are the key issues. Much of the recent commercial R&D has emphasized commercially available, inert, microbial biomass sources as these can be acquired in sufficient quantities at affordable costs. The fundamental research and practical applications of bioaccumulation by microalgae suggests these organisms warrant a high priority in the development of advanced bioremoval processes.

Benemann, J.R. [Benemann (J.R.), Pinole, CA (United States); Wilde, E.W. [Westinghouse Savannah River Co., Aiken, SC (United States)

1991-02-01T23:59:59.000Z

7

Literature review on the use of bioaccumulation for heavy metal removal and recovery  

SciTech Connect

Bioaccumulation of metals by microbes -- bioremoval'' -- is a powerful new technology for the concentration, recovery, and removal of toxic heavy metals and radionuclides from waste streams and contaminated environments. Algae are particularly well suited for metal bioremoval. A recent commercial application of bioremoval utilizes inert (dead) immobilized microalgae biomass as ion exchange materials for the removal of heavy metals from industrial waste waters. Also, living microalgal cultures have been used to remove metals from mine effluents. Microbial cells and biomass can bioaccumulate metals and radionuclides by a large variety of mechanisms, both dependent and independent of cell metabolism. Microbial cell walls can act as ion exchange and metal complexation agents. Heavy metals can precipitate and even crystallize on cell surfaces. Metabolically produced hydrogen sulfide or other metabolic products can bioprecipitate heavy metals. Many microbes produce both intra- and extracellular metal complexing agents which could be considered in practical metal removal processes. Bioremoval processes are greatly affected by the microbial species and even strain used, pH, redox potential, temperature, and other conditions under which the microbes are grown. Development of practical applications of bioremoval requires applies research using the particular waste solutions to be treated, or close simulations thereof. From a practical perspective, the selection of the microbial biomass and the process for contacting the microbial biomass with the metal containing solutions are the key issues. Much of the recent commercial R D has emphasized commercially available, inert, microbial biomass sources as these can be acquired in sufficient quantities at affordable costs. The fundamental research and practical applications of bioaccumulation by microalgae suggests these organisms warrant a high priority in the development of advanced bioremoval processes.

Benemann, J.R. (Benemann (J.R.), Pinole, CA (United States)); Wilde, E.W. (Westinghouse Savannah River Co., Aiken, SC (United States))

1991-02-01T23:59:59.000Z

8

Method for removing heavy metal and nitrogen oxides from flue gas, device for removing heavy metal and nitrogen oxides from flue gas  

DOE Patents (OSTI)

A method for the simultaneous removal of oxides and heavy metals from a fluid is provided comprising combining the fluid with compounds containing alkali and sulfur to create a mixture; spray drying the mixture to create a vapor phase and a solid phase; and isolating the vapor phase from the solid phase. A device is also provided comprising a means for spray-drying flue gas with alkali-sulfide containing liquor at a temperature sufficient to cause the flue gas to react with the compounds so as to create a gaseous fraction and a solid fraction and a means for directing the gaseous fraction to a fabric filter.

Huang, Hann-Sheng; Livengood, Charles David

1997-12-01T23:59:59.000Z

9

Removal of radioactive materials and heavy metals from water using magnetic resin  

DOE Patents (OSTI)

Magnetic polymer resins capable of efficient removal of actinides and heavy metals from contaminated water are disclosed together with methods for making, using, and regenerating them. The resins comprise polyamine-epichlorohydrin resin beads with ferrites attached to the surfaces of the beads. Markedly improved water decontamination is demonstrated using these magnetic polymer resins of the invention in the presence of a magnetic field, as compared with water decontamination methods employing ordinary ion exchange resins or ferrites taken separately.

Kochen, Robert L. (Boulder, CO); Navratil, James D. (Simi Valley, CA)

1997-01-21T23:59:59.000Z

10

Removal of heavy metal ions from oil shale beneficiation process water by ferrite process  

SciTech Connect

The ferrite process is an established technique for removing heavy metals from waste water. Because the process water resulting from oil shale beneficiation falls into the category of industrial waste water, it is anticipated that this process may turn out to be a potential viable treatment for oil shale beneficiation process water containing many heave metal ions. The process is chemoremedial because not only effluent water comply with quality standards, but harmful heavy metals are converted into a valuable, chemically stable by-product known as ferrite. These spinel ferrites have magnetic properties, and therefore can be use in applications such as magnetic marker, ferrofluid, microwave absorbing and scavenging material. Experimental results from this process are presented along with results of treatment technique such as sulfide precipitation.

Mehta, R.K.; Zhang, L.; Lamont, W.E.; Schultz, C.W. (Alabama Univ., University, AL (United States). Mineral Resources Inst.)

1991-01-01T23:59:59.000Z

11

Removal of heavy metal ions from oil shale beneficiation process water by ferrite process  

SciTech Connect

The ferrite process is an established technique for removing heavy metals from waste water. Because the process water resulting from oil shale beneficiation falls into the category of industrial waste water, it is anticipated that this process may turn out to be a potential viable treatment for oil shale beneficiation process water containing many heave metal ions. The process is chemoremedial because not only effluent water comply with quality standards, but harmful heavy metals are converted into a valuable, chemically stable by-product known as ferrite. These spinel ferrites have magnetic properties, and therefore can be use in applications such as magnetic marker, ferrofluid, microwave absorbing and scavenging material. Experimental results from this process are presented along with results of treatment technique such as sulfide precipitation.

Mehta, R.K.; Zhang, L.; Lamont, W.E.; Schultz, C.W. [Alabama Univ., University, AL (United States). Mineral Resources Inst.

1991-12-31T23:59:59.000Z

12

Separation of heavy metals: Removal from industrial wastewaters and contaminated soil  

Science Conference Proceedings (OSTI)

This paper reviews the applicable separation technologies relating to removal of heavy metals from solution and from soils in order to present the state-of-the-art in the field. Each technology is briefly described and typical operating conditions and technology performance are presented. Technologies described include chemical precipitation (including hydroxide, carbonate, or sulfide reagents), coagulation/flocculation, ion exchange, solvent extraction, extraction with chelating agents, complexation, electrochemical operation, cementation, membrane operations, evaporation, adsorption, solidification/stabilization, and vitrification. Several case histories are described, with a focus on waste reduction techniques and remediation of lead-contaminated soils. The paper concludes with a short discussion of important research needs in the field.

Peters, R.W.; Shem, L.

1993-03-01T23:59:59.000Z

13

Separation of heavy metals: Removal from industrial wastewaters and contaminated soil  

SciTech Connect

This paper reviews the applicable separation technologies relating to removal of heavy metals from solution and from soils in order to present the state-of-the-art in the field. Each technology is briefly described and typical operating conditions and technology performance are presented. Technologies described include chemical precipitation (including hydroxide, carbonate, or sulfide reagents), coagulation/flocculation, ion exchange, solvent extraction, extraction with chelating agents, complexation, electrochemical operation, cementation, membrane operations, evaporation, adsorption, solidification/stabilization, and vitrification. Several case histories are described, with a focus on waste reduction techniques and remediation of lead-contaminated soils. The paper concludes with a short discussion of important research needs in the field.

Peters, R.W.; Shem, L.

1993-01-01T23:59:59.000Z

14

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

DOE Patents (OSTI)

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

Gay, E.C.

1993-12-23T23:59:59.000Z

15

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

DOE Patents (OSTI)

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

Gay, Eddie C. (Park Forest, IL)

1995-01-01T23:59:59.000Z

16

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

DOE Patents (OSTI)

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

Gay, E.C.

1995-10-03T23:59:59.000Z

17

Removal of heavy metals from aqueous waste streams using surface-modified nanosized TiO{sub 2} photocatalysts.  

DOE Green Energy (OSTI)

Titanium dioxide (TiO{sub 2}) colloidal particles ({approximately}45{angstrom}) whose surfaces were modified with chelating agents for photocatalytic removal of heavy-metal ions and their subsequent reduction to metallic form were investigated. Experiments were performed on nanoparticle TiO{sub 2} colloids derivatized with bidentate and tridentate ligands (thiolactic acid [TLA], cysteine, and alanine [ALA]) in batch mode in a photoreactor with 254nm light. We used catalysts designed and synthesized for selective and efficient removal of Pb and Cu with and without added hole scavenger (methanol). Parallel experiments also have been carried out in the dark to study metal ion adsorption properties. Solutions have been filtered to remove TiO{sub 2}, and metal particulates. Both the native solution and the metal deposited on the nanocrystalline TiO{sub 2} particles were analyzed. Results demonstrate that for the case of lead, the most effective TiO{sub 2} surface modifier was TLA (>99% Pb(II) removed from solution). Experiments performed to study Cn removal using TiO{sub 2} colloids modified with alanine showed that copper ions were effectively removed and reduced to metallic form in the presence of methanol.

Meshkov, N. K.

1998-08-27T23:59:59.000Z

18

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

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

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

1988-08-26T23:59:59.000Z

19

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

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

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

1990-01-01T23:59:59.000Z

20

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

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

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

1990-11-13T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Plant rhamnogalacturonan II complexation of heavy metal cations  

DOE Patents (OSTI)

The present invention provides rhamnogalacturonan-II (RG-II) and relates to its ability to complex specific multivalent heavy metal cations. In the presence of boric acid, RG-II monomers form dimers that are cross-linked by a borate ester. The yield of such borate ester cross-linked dimers of RG-II is enhanced in the presence of specific heavy metal cations. The present invention further relates to the utility of RG-II in assays for the detection of specific heavy metal contamination; as a reagent useful in the removal of specific heavy metal cations contaminating foods and liquids, for example, fish, wines, etc.; as a pharmaceutical composition useful as an antidote in specific heavy metal cation poisoning; as a treatment for the detoxification of specific heavy metal cations from blood and/or tissues; and in a method of remediation of waters and soils contaminated with specific heavy metal cations.

O' Neill, Malcolm A. (Winterville, GA); Pellerin, Patrice J. M. (Montpellier, FR); Warrenfeltz, Dennis (Athens, GA); Vidal, Stephane (Combaillaux, FR); Darvill, Alan G. (Athens, GA); Albersheim, Peter (Athens, GA)

1999-01-01T23:59:59.000Z

22

Plant rhamnogalacturonan II complexation of heavy metal cations  

DOE Patents (OSTI)

The present invention provides rhamnogalacturonan-II (RG-II) and relates to its ability to complex specific multivalent heavy metal cations. In the presence of boric acid, RG-II monomers form dimers that are cross-linked by a borate ester. The yield of such borate ester cross-linked dimers of RG-II is enhanced in the presence of specific heavy metal cations. The present invention further relates to the utility of RG-II in assays for the detection of specific heavy metal contamination; as a reagent useful in the removal of specific heavy metal cations contaminating foods and liquids, for example, fish, wines, etc.; as a pharmaceutical composition useful as an antidote in specific heavy metal cation poisoning; as a treatment for the detoxification of specific heavy metal cations from blood and/or tissues; and in a method of remediation of waters and soils contaminated with specific heavy metal cations. 15 figs.

O`Neill, M.A.; Pellerin, P.J.M.; Warrenfeltz, D.; Vidal, S.; Darvill, A.G.; Albersheim, P.

1999-03-02T23:59:59.000Z

23

Biosorption beads for removal of dissolved metals from aqueous streams  

DOE Patents (OSTI)

This invention is comprised of a process for removing heavy metals from aqueous waste streams 5 by contacting such streams with certain biological adsorbents, either living, dead or in fragments, that may be immobilized in gel beads. 1 tab.

Scott, C.D.

1988-01-21T23:59:59.000Z

24

Metals removal from spent salts  

DOE Patents (OSTI)

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

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

2002-01-01T23:59:59.000Z

25

Heavy metals hazardous components of Eaf dust  

Science Conference Proceedings (OSTI)

Electric arc furnace (EAF) dust is a waste generated in the EAF during the steel production process. Among different wastes, EAF dust represents one of the most hazardous, since it contains heavy metals such as Zn, Fe, Cr, Cd and Pb. The goal of the ... Keywords: electric arc furnace (EAF), furnace additives, hazard components, heavy metals, scrap composition, x-ray fluorescence spectroscopy

Cristiana-Zizi Rizescu; Zorica Bacinschi; Elena Valentina Stoian; Aurora Poinescu; Dan Nicolae Ungureanu

2011-02-01T23:59:59.000Z

26

Heavy metals in suspended powders from steelmaking  

Science Conference Proceedings (OSTI)

Motivations for controlling heavy metal concentrations in gas streams are diverse. Some of them are dangerous to health or to the environment (e.g. Hg, Cd, As, Pb, Cr), some may cause corrosion (e.g. Zn, Pb), some are harmful in other ways (e.g. Arsenic ... Keywords: anthropogenic sources, emissions, heavy metals, human health, pollution of ecosystem, toxic

Cristiana-Zizi Rizescu; Elena-Valentina Stoian; Aurora-Anca Poinescu; Sofia Teodorescu

2010-07-01T23:59:59.000Z

27

Attrition resistant catalysts and sorbents based on heavy metal poisoned FCC catalysts  

DOE Patents (OSTI)

A heavy metal poisoned, spent FCC catalyst is treated by chemically impregnating the poisoned catalyst with a new catalytic metal or metal salt to provide an attrition resistant catalyst or sorbent for a different catalytic or absorption processes, such as catalysts for Fischer-Tropsh Synthesis, and sorbents for removal of sulfur gasses from fuel gases and flue-gases. The heavy metal contaminated FCC catalyst is directly used as a support for preparing catalysts having new catalytic properties and sorbents having new sorbent properties, without removing or "passivating" the heavy metals on the spent FCC catalyst as an intermediate step.

Gangwal, Santosh (Cary, NC); Jothimurugesan, Kandaswamy (Hampton, VA)

1999-01-01T23:59:59.000Z

28

Attrition resistant catalysts and sorbents based on heavy metal poisoned FCC catalysts  

DOE Patents (OSTI)

A heavy metal poisoned, spent FCC catalyst is treated by chemically impregnating the poisoned catalyst with a new catalytic metal or metal salt to provide an attrition resistant catalyst or sorbent for a different catalytic or absorption process, such as catalysts for Fischer-Tropsh Synthesis, and sorbents for removal of sulfur gases from fuel gases and flue-gases. The heavy metal contaminated FCC catalyst is directly used as a support for preparing catalysts having new catalytic properties and sorbents having new sorbent properties, without removing or passivating the heavy metals on the spent FCC catalyst as an intermediate step.

Gangwal, S.; Jothimurugesan, K.

1999-07-27T23:59:59.000Z

29

Experimental Research on Recovery of Heavy Metals from EAF ...  

Science Conference Proceedings (OSTI)

To recycle these heavy metals, it is quite important to know the reactivity and metallurgical behavior of these heavy metals contained in EAF stainless steel dust.

30

Assessment of heavy metal contamination of roadside soils in ...  

Science Conference Proceedings (OSTI)

Feb 16, 2008 ... heavy metals was found using factor analysis. Keywords Heavy metals Á Roadside soils Á. Transportation period Á Contamination index Á.

31

Extraction process for removing metallic impurities from alkalide metals  

DOE Patents (OSTI)

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

Royer, Lamar T. (Knoxville, TN)

1988-01-01T23:59:59.000Z

32

Extraction process for removing metallic impurities from alkalide metals  

DOE Patents (OSTI)

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

Royer, L.T.

1987-03-20T23:59:59.000Z

33

Catalyst regeneration process including metal contaminants removal  

DOE Patents (OSTI)

Spent catalysts removed from a catalytic hydrogenation process for hydrocarbon feedstocks, and containing undesired metals contaminants deposits, are regenerated. Following solvent washing to remove process oils, the catalyst is treated either with chemicals which form sulfate or oxysulfate compounds with the metals contaminants, or with acids which remove the metal contaminants, such as 5-50 W % sulfuric acid in aqueous solution and 0-10 W % ammonium ion solutions to substantially remove the metals deposits. The acid treating occurs within the temperature range of 60.degree.-250.degree. F. for 5-120 minutes at substantially atmospheric pressure. Carbon deposits are removed from the treated catalyst by carbon burnoff at 800.degree.-900.degree. F. temperature, using 1-6 V % oxygen in an inert gas mixture, after which the regenerated catalyst can be effectively reused in the catalytic process.

Ganguli, Partha S. (Lawrenceville, NJ)

1984-01-01T23:59:59.000Z

34

Treatment of Heavy Metal Wastes - III - TMS  

Science Conference Proceedings (OSTI)

Ltd., Flin Fion, Manitoba, Canada R8A 1N9. 3:15 pm BREAK. 3:30 pm. An Integrated Bioremediation Route for Heavy Metal Contaminated Land Based on the ...

35

Method for removing metal ions from solution with titanate sorbents  

DOE Patents (OSTI)

A method for removing metal ions from solution comprises the steps of providing titanate particles by spray-drying a solution or slurry comprising sorbent titanates having a particle size up to 20 micrometers, optionally in the presence of polymer free of cellulose functionality as binder, said sorbent being active towards heavy metals from Periodic Table (CAS version) Groups IA, IIA, IB, IIB, IIIB, and VIII, to provide monodisperse, substantially spherical particles in a yield of at least 70 percent of theoretical yield and having a particle size distribution in the range of 1 to 500 micrometers. The particles can be used free flowing in columns or beds, or entrapped in a nonwoven, fibrous web or matrix or a cast porous membrane, to selectively remove metal ions from aqueous or organic liquid.

Lundquist, Susan H. (White Bear Township, MN); White, Lloyd R. (Minneapolis, MN)

1999-01-01T23:59:59.000Z

36

Process for removing metals from water  

DOE Patents (OSTI)

A process for removing metals from water including the steps of prefiltering solids from the water, adjusting the pH to between about 2 and 3, reducing the amount of dissolved oxygen in the water, increasing the pH to between about 6 and 8, adding water-soluble sulfide to precipitate insoluble sulfide- and hydroxide-forming metals, adding a containing floc, and postfiltering the resultant solution. The postfiltered solution may optionally be eluted through an ion exchange resin to remove residual metal ions. 2 tabs.

Napier, J.M.; Hancher, C.M.; Hackett, G.D.

1987-06-29T23:59:59.000Z

37

Regenerative process for removal of mercury and other heavy metals from gases containing H.sub.2 and/or CO  

DOE Patents (OSTI)

A method for removal of mercury from a gaseous stream containing the mercury, hydrogen and/or CO, and hydrogen sulfide and/or carbonyl sulfide in which a dispersed Cu-containing sorbent is contacted with the gaseous stream at a temperature in the range of about 25.degree. C. to about 300.degree. C. until the sorbent is spent. The spent sorbent is contacted with a desorbing gaseous stream at a temperature equal to or higher than the temperature at which the mercury adsorption is carried out, producing a regenerated sorbent and an exhaust gas comprising released mercury. The released mercury in the exhaust gas is captured using a high-capacity sorbent, such as sulfur-impregnated activated carbon, at a temperature less than about 100.degree. C. The regenerated sorbent may then be used to capture additional mercury from the mercury-containing gaseous stream.

Jadhav, Raja A. (Naperville, IL)

2009-07-07T23:59:59.000Z

38

Biological removal of metal ions from aqueous process streams  

SciTech Connect

Aqueous waste streams from nuclear fuel processing operations may contain trace quantities of heavy metals such as uranium. Conventional chemical and physical treatment may be ineffective or very expensive when uranium concentrations in the range of 10 to 100 g/m/sup 3/ must be reduced to 1 g/m/sup 3/ or less. The ability of some microorganisms to adsorb or complex dissolved heavy metals offers an alternative treatment method. Uranium uptake by Saccharomyces cerevisiae NRRL Y-2574 and a strain of Pseudomonas aeruginosa was examined to identify factors which might affect a process for the removal of uranium from wastewater streams. At uranium concentrations in the range of 10 to 500 g/m/sup 3/, where the binding capacity of the biomass was not exceeded, temperature, pH, and initial uranium concentration were found to influence the rate of uranium uptake, but not the soluble uranium concentration at equilibrium. 6 figs.

Shumate, S.E. II; Strandberg, G.W.; Parrott, J.R. Jr.

1978-01-01T23:59:59.000Z

39

Heavy metals behaviour in a gasification reactor  

Science Conference Proceedings (OSTI)

Sludge coming from cleaning processes of wastewater, Municipal Solid Waste (MSW), and Refuse Derived Fuel (RDF) can be exploited for producing energy because of their heating value. Cleaning the produced syngas is important because of environmental troubles, ... Keywords: heavy metals, syngas, thermodynamic, waste gasification

Martino Paolucci; Carlo Borgianni; Paolo De Filippis

2011-07-01T23:59:59.000Z

40

Situ formation of apatite for sequestering radionuclides and heavy metals  

DOE Patents (OSTI)

Methods for in situ formation in soil of a permeable reactive barrier or zone comprising a phosphate precipitate, such as apatite or hydroxyapatite, which is capable of selectively trapping and removing radionuclides and heavy metal contaminants from the soil, while allowing water or other compounds to pass through. A preparation of a phosphate reagent and a chelated calcium reagent is mixed aboveground and injected into the soil. Subsequently, the chelated calcium reagent biodegrades and slowly releases free calcium. The free calcium reacts with the phosphate reagent to form a phosphate precipitate. Under the proper chemical conditions, apatite or hydroxyapatite can form. Radionuclide and heavy metal contaminants, including lead, strontium, lanthanides, and uranium are then selectively sequestered by sorbing them onto the phosphate precipitate. A reducing agent can be added for reduction and selective sequestration of technetium or selenium contaminants.

Moore, Robert C. (Edgewood, NM)

2003-07-15T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Removal of Retired Alkali Metal Test Systems  

SciTech Connect

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

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

2003-02-26T23:59:59.000Z

42

Process for removing technetium from iron and other metals  

DOE Patents (OSTI)

A process for removing technetium from iron and other metals comprises the steps of converting the molten, alloyed technetium to a sulfide dissolved in manganese sulfide, and removing the sulfide from the molten metal as a slag. 4 figs.

Leitnaker, J.M.; Trowbridge, L.D.

1999-03-23T23:59:59.000Z

43

Process for removing technetium from iron and other metals  

DOE Patents (OSTI)

A process for removing technetium from iron and other metals comprises the steps of converting the molten, alloyed technetium to a sulfide dissolved in manganese sulfide, and removing the sulfide from the molten metal as a slag.

Leitnaker, James M. (Kingston, TN); Trowbridge, Lee D. (Oak Ridge, TN)

1999-01-01T23:59:59.000Z

44

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

DOE Patents (OSTI)

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

Gorin, Everett (San Rafael, CA)

1979-01-01T23:59:59.000Z

45

Heavy Metals Behavior of Municiple Solid Waste Incineration ... - TMS  

Science Conference Proceedings (OSTI)

May 1, 2007 ... Heavy Metals Behavior of Municiple Solid Waste Incineration Bottom Ash with Magnetic Separation by Gi-Chun Han, Nam-Il Um, Kwang-Suk ...

46

Heavy Water Components Test Reactor Decommissioning - Major Component Removal  

SciTech Connect

The Heavy Water Components Test Reactor (HWCTR) facility (Figure 1) was built in 1961, operated from 1962 to 1964, and is located in the northwest quadrant of the Savannah River Site (SRS) approximately three miles from the site boundary. The HWCTR facility is on high, well-drained ground, about 30 meters above the water table. The HWCTR was a pressurized heavy water test reactor used to develop candidate fuel designs for heavy water power reactors. It was not a defense-related facility like the materials production reactors at SRS. The reactor was moderated with heavy water and was rated at 50 megawatts thermal power. In December of 1964, operations were terminated and the facility was placed in a standby condition as a result of the decision by the U.S. Atomic Energy Commission to redirect research and development work on heavy water power reactors to reactors cooled with organic materials. For about one year, site personnel maintained the facility in a standby status, and then retired the reactor in place. In 1965, fuel assemblies were removed, systems that contained heavy water were drained, fluid piping systems were drained, deenergized and disconnected and the spent fuel basin was drained and dried. The doors of the reactor facility were shut and it wasn't until 10 years later that decommissioning plans were considered and ultimately postponed due to budget constraints. In the early 1990s, DOE began planning to decommission HWCTR again. Yet, in the face of new budget constraints, DOE deferred dismantlement and placed HWCTR in an extended surveillance and maintenance mode. The doors of the reactor facility were welded shut to protect workers and discourage intruders. The $1.6 billion allocation from the American Recovery and Reinvestment Act to SRS for site clean up at SRS has opened the doors to the HWCTR again - this time for final decommissioning. During the lifetime of HWCTR, 36 different fuel assemblies were tested in the facility. Ten of these experienced cladding failures as operational capabilities of the different designs were being established. In addition, numerous spills of heavy water occurred within the facility. Currently, radiation and radioactive contamination levels are low within HWCTR with most of the radioactivity contained within the reactor vessel. There are no known insults to the environment, however with the increasing deterioration of the facility, the possibility exists that contamination could spread outside the facility if it is not decommissioned. An interior panoramic view of the ground floor elevation taken in August 2009 is shown in Figure 2. The foreground shows the transfer coffin followed by the reactor vessel and control rod drive platform in the center. Behind the reactor vessel is the fuel pool. Above the ground level are the polar crane and the emergency deluge tank at the top of the dome. Note the considerable rust and degradation of the components and the interior of the containment building. Alternative studies have concluded that the most environmentally safe, cost effective option for final decommissioning is to remove the reactor vessel, steam generators, and all equipment above grade including the dome. Characterization studies along with transport models have concluded that the remaining below grade equipment that is left in place including the transfer coffin will not contribute any significant contamination to the environment in the future. The below grade space will be grouted in place. A concrete cover will be placed over the remaining footprint and the groundwater will be monitored for an indefinite period to ensure compliance with environmental regulations. The schedule for completion of decommissioning is late FY2011. This paper describes the concepts planned in order to remove the major components including the dome, the reactor vessel (RV), the two steam generators (SG), and relocating the transfer coffin (TC).

Austin, W.; Brinkley, D.

2010-05-05T23:59:59.000Z

47

Heavy Water Components Test Reactor Decommissioning - Major Component Removal  

SciTech Connect

The Heavy Water Components Test Reactor (HWCTR) facility (Figure 1) was built in 1961, operated from 1962 to 1964, and is located in the northwest quadrant of the Savannah River Site (SRS) approximately three miles from the site boundary. The HWCTR facility is on high, well-drained ground, about 30 meters above the water table. The HWCTR was a pressurized heavy water test reactor used to develop candidate fuel designs for heavy water power reactors. It was not a defense-related facility like the materials production reactors at SRS. The reactor was moderated with heavy water and was rated at 50 megawatts thermal power. In December of 1964, operations were terminated and the facility was placed in a standby condition as a result of the decision by the U.S. Atomic Energy Commission to redirect research and development work on heavy water power reactors to reactors cooled with organic materials. For about one year, site personnel maintained the facility in a standby status, and then retired the reactor in place. In 1965, fuel assemblies were removed, systems that contained heavy water were drained, fluid piping systems were drained, deenergized and disconnected and the spent fuel basin was drained and dried. The doors of the reactor facility were shut and it wasn't until 10 years later that decommissioning plans were considered and ultimately postponed due to budget constraints. In the early 1990s, DOE began planning to decommission HWCTR again. Yet, in the face of new budget constraints, DOE deferred dismantlement and placed HWCTR in an extended surveillance and maintenance mode. The doors of the reactor facility were welded shut to protect workers and discourage intruders. The $1.6 billion allocation from the American Recovery and Reinvestment Act to SRS for site clean up at SRS has opened the doors to the HWCTR again - this time for final decommissioning. During the lifetime of HWCTR, 36 different fuel assemblies were tested in the facility. Ten of these experienced cladding failures as operational capabilities of the different designs were being established. In addition, numerous spills of heavy water occurred within the facility. Currently, radiation and radioactive contamination levels are low within HWCTR with most of the radioactivity contained within the reactor vessel. There are no known insults to the environment, however with the increasing deterioration of the facility, the possibility exists that contamination could spread outside the facility if it is not decommissioned. An interior panoramic view of the ground floor elevation taken in August 2009 is shown in Figure 2. The foreground shows the transfer coffin followed by the reactor vessel and control rod drive platform in the center. Behind the reactor vessel is the fuel pool. Above the ground level are the polar crane and the emergency deluge tank at the top of the dome. Note the considerable rust and degradation of the components and the interior of the containment building. Alternative studies have concluded that the most environmentally safe, cost effective option for final decommissioning is to remove the reactor vessel, steam generators, and all equipment above grade including the dome. Characterization studies along with transport models have concluded that the remaining below grade equipment that is left in place including the transfer coffin will not contribute any significant contamination to the environment in the future. The below grade space will be grouted in place. A concrete cover will be placed over the remaining footprint and the groundwater will be monitored for an indefinite period to ensure compliance with environmental regulations. The schedule for completion of decommissioning is late FY2011. This paper describes the concepts planned in order to remove the major components including the dome, the reactor vessel (RV), the two steam generators (SG), and relocating the transfer coffin (TC).

Austin, W.; Brinkley, D.

2010-05-05T23:59:59.000Z

48

Limitations for heavy metal release during thermo-chemical treatment of sewage sludge ash  

Science Conference Proceedings (OSTI)

Phosphate recycling from sewage sludge can be achieved by heavy metal removal from sewage sludge ash (SSA) producing a fertilizer product: mixing SSA with chloride and treating this mixture (eventually after granulation) in a rotary kiln at 1000 {+-} 100 deg. C leads to the formation of volatile heavy metal compounds that evaporate and to P-phases with high bio-availability. Due to economical and ecological reasons, it is necessary to reduce the energy consumption of this technology. Generally, fluidized bed reactors are characterized by high heat and mass transfer and thus promise the saving of energy. Therefore, a rotary reactor and a fluidized bed reactor (both laboratory-scale and operated in batch mode) are used for the treatment of granulates containing SSA and CaCl{sub 2}. Treatment temperature, residence time and - in case of the fluidized bed reactor - superficial velocity are varied between 800 and 900 deg. C, 10 and 30 min and 3.4 and 4.6 m s{sup -1}. Cd and Pb can be removed well (>95 %) in all experiments. Cu removal ranges from 25% to 84%, for Zn 75-90% are realized. The amount of heavy metals removed increases with increasing temperature and residence time which is most pronounced for Cu. In the pellet, three major reactions occur: formation of HCl and Cl{sub 2} from CaCl{sub 2}; diffusion and reaction of these gases with heavy metal compounds; side reactions from heavy metal compounds with matrix material. Although, heat and mass transfer are higher in the fluidized bed reactor, Pb and Zn removal is slightly better in the rotary reactor. This is due the accelerated migration of formed HCl and Cl{sub 2} out of the pellets into the reactor atmosphere. Cu is apparently limited by the diffusion of its chloride thus the removal is higher in the fluidized bed unit.

Nowak, Benedikt, E-mail: benedikt.nowak@tuwien.ac.at [Institute of Chemical Engineering, Vienna University of Technology, Getreidemarkt 9/166, A-1060 Vienna (Austria); Perutka, Libor [Institute of Chemical Engineering, Vienna University of Technology, Getreidemarkt 9/166, A-1060 Vienna (Austria); Aschenbrenner, Philipp [Institute for Water Quality, Resource and Waste Management, Vienna University of Technology, Karlsplatz 13/226, A-1040 Vienna (Austria); Kraus, Petra [ASH DEC Umwelt AG, Donaufelderstrasse 101/4/5, A-1210 Vienna (Austria); Rechberger, Helmut [Institute for Water Quality, Resource and Waste Management, Vienna University of Technology, Karlsplatz 13/226, A-1040 Vienna (Austria); Winter, Franz, E-mail: franz.winter@tuwien.ac.at [Institute of Chemical Engineering, Vienna University of Technology, Getreidemarkt 9/166, A-1060 Vienna (Austria)

2011-06-15T23:59:59.000Z

49

PROCESS FOR SEPARATION OF HEAVY METALS  

DOE Patents (OSTI)

A method is described for separating plutonium from aqueous acidic solutions of neutron-irradiated uranium and the impurities associated therewith. The separation is effected by adding, to the solution containing hexavalent uranium and plutonium, acetate ions and the ions of an alkali metal and those of a divalent metal and thus forming a complex plutonium acetate salt which is carried by the corresponding complex of uranium, such as sodium magnesium uranyl acetate. The plutonium may be separated from the precipitated salt by taking the same back into solution, reducing the plutonium to a lower valent state on reprecipitating the sodium magnesium uranyl salt, removing the latter, and then carrying the plutonium from ihe solution by means of lanthanum fluoride.

Duffield, R.B.

1958-04-29T23:59:59.000Z

50

Metal Cutting for Large Component Removal  

Science Conference Proceedings (OSTI)

Decommissioning of commercial nuclear power plants presents technological challenges. One major challenge is the removal of large components mainly consisting of the reactor vessel, steam generators and pressurizer. In order to remove and package these large components nozzles must be cut from the reactor vessel to precise tolerances. In some cases steam generators must be segmented for size and weight reduction. One innovative technology that has been used successfully at several commercial nuclear plant decommissioning is diamond wire sawing. Diamond wire sawing is performed by rotating a cable with diamond segments attached using a flywheel approximately 24 inches in diameter driven remotely by a hydraulic pump. Tension is provided using a gear rack drive which also takes up the slack in the wire. The wire is guided through the use of pulleys keeps the wire in a precise location. The diamond wire consists of 1/4 inch aircraft cable with diamond beads strung over the cable separated by springs and brass crimps. Standard wire contains 40 diamond beads per meter and can be made to any length. Cooling the wire and controlling the spread of contamination presents significant challenges. Under normal circumstances the wire is cooled and the cutting kerf cleaned by using water. In some cases of reactor nozzle cuts the use of water is prohibited because it cannot be controlled. This challenge was solved by using liquid Carbon Dioxide as the cooling agent. The liquid CO{sub 2} is passed through a special nozzle which atomizes the liquid into snowflakes which is introduced under pressure to the wire. The snowflakes attach to the wire keeping it cool and to the metal shavings. As the CO{sub 2} and metal shavings are released from the wire due to its fast rotation, the snowflakes evaporate leaving only the fine metal shavings as waste. Secondary waste produced is simply the small volume of fine metal shavings removed from the cut surface. Diamond wire sawing using CO{sub 2} cooling has been employed for cutting the reactor nozzles at San Onofre Unit 1 and at Connecticut Yankee. These carbon steel nozzles ranged up to 54 inch diameter with a 15 inch thick wall and an interior stainless cladding. Diamond wire sawing using traditional water cooling has been used to segment the reactor head at Rancho Seco and for cutting reactor nozzles and control rod drive tubes at Dairyland Power's Lacrosse BWR project. Advantages: - ALARA: All cutting is preformed remotely significantly reducing dose. Stringing of wires is accomplished using long handle tools. - Secondary waste is reduced to just the volume of material cut with the diamond wire. - The potential for airborne contamination is eliminated. Due to the flexibility of the wire, any access restrictions and interferences can be accommodated using pulleys and long handle tools. - The operation is quiet. Disadvantages: - With Liquid Carbon Dioxide cooling and cleaning, delivery of the material must be carefully planned. The longer the distance from the source to the cut area, the greater the chance for pressure drop and subsequent problems with line freezing. - Proper shrouding and ventilation are required for environmental reasons. In each case, the metal structures were cut at a precise location. Radiation dose was reduced significantly by operating the equipment from a remote location. The cuts were very smooth and completed on schedule. Each project must be analyzed individually and take into account many factors including access, radiological conditions, environmental conditions, schedule requirements, packaging requirements and size of cuts.

Hulick, Robert M. [Bluegrass Concrete Cutting Inc., 107 Mildred Street PO Box 427, Greenville, Alabama 36037 (United States)

2008-01-15T23:59:59.000Z

51

Tons of Heavy Metals in Mill Creek Sediments Heather Freeman  

E-Print Network (OSTI)

with industries. Paper, woolen, flour, and cotton mills, starch factories, slaughterhouses, distilleriesTons of Heavy Metals in Mill Creek Sediments Heather Freeman 8/30/99 Geology Department Advisors: Dr. Kees DeJong Dr. Barry Manyard Dr. David Nash #12;Tons of heavy metals in Mill Creek sediments

Maynard, J. Barry

52

Modeling heavy metal mass releases from urban battery litter  

Science Conference Proceedings (OSTI)

Consumer batteries littered on urban pavements release metals of environmental significance (Ag, Cd, Cr, Cu, Hg, Li, Mn, Ni, Pd, Ti, Zn) to stormwater runoff. Predicting the mass loading of any one metal is difficult because of the random composition ... Keywords: Heavy metals, filtered Poisson process, Mass loading, zinc, Stormwater contamination, Urban battery litter

Caleb Krouse; Aaron A. Jennings; Dario Gasparini

2009-04-01T23:59:59.000Z

53

Heavy Liquid Metal Reactor Development - Nuclear Engineering Division  

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

> Heavy Liquid Metal Reactor Development > Heavy Liquid Metal Reactor Development Capabilities Nuclear Systems Modeling and Design Analysis Reactor Physics and Fuel Cycle Analysis Nuclear Data Program Advanced Reactor Development Overview Advanced Fast Reactor (AFR) Heavy Liquid Metal Reactor Development Generation IV Nuclear Waste Form and Repository Performance Modeling Nuclear Energy Systems Design and Development Other Capabilities Work with Argonne Contact us For Employees Site Map Help Advanced Reactor Development and Technology Heavy Liquid Metal Reactor Development Bookmark and Share STAR-LM: Simplified, Modular, Small Reactor Featuring Flow-thru Fuel Cartridge STAR-LM: Simplified, Modular, Small Reactor Featuring Flow-thru Fuel Cartridge. Click on image to view larger image. Argonne has traditionally been the foremost institute in the US for

54

Modeling of Heavy Metals Ions Adsorption by Polyamidoamine ...  

Science Conference Proceedings (OSTI)

... that employ PAMAM dendrimers for adsorption of heavy metals from wastewater. ... Heat Treatment of Black Dross for the Production of a Value Added Material ... Mullites Bodies Produced From the Kaolin Residue Using Microwave Energy.

55

Metal Organic Clathrates for Carbon Dioxide Removal  

removal from coal-fired power plant flue gas streams.  Modified variations of the materials can be used in a variety of other fields as well, ...

56

Removal of field and embedded metal by spin spray etching  

SciTech Connect

A process of removing both the field metal, such as copper, and a metal, such as copper, embedded into a dielectric or substrate at substantially the same rate by dripping or spraying a suitable metal etchant onto a spinning wafer to etch the metal evenly on the entire surface of the wafer. By this process the field metal is etched away completely while etching of the metal inside patterned features in the dielectric at the same or a lesser rate. This process is dependent on the type of chemical etchant used, the concentration and the temperature of the solution, and also the rate of spin speed of the wafer during the etching. The process substantially reduces the metal removal time compared to mechanical polishing, for example, and can be carried out using significantly less expensive equipment.

Contolini, Robert J. (Pleasanton, CA); Mayer, Steven T. (San Leandro, CA); Tarte, Lisa A. (Livermore, CA)

1996-01-01T23:59:59.000Z

57

Improvement of Plants for Selenium and Heavy Metal Phytoremediation Through Genetic Engineering  

Science Conference Proceedings (OSTI)

Phytoremediation -- the use of plants to remove, stabilize, or detoxify pollutants -- has proved very promising for the cleanup of trace elements from contaminated soil and water. Under the EPRI-Genetics Research Program, investigators successfully used genetic engineering to create seven genetically altered lines of plants with superior capacities for the phytoremediation of selenium (Se) and heavy metals, such as Molybdenum (Mo), Tungsten (W), and Cadmium (Cd). These transgenic plants are more tolerant...

1999-12-13T23:59:59.000Z

58

Process for removing technetium from iron and other metals  

DOE Patents (OSTI)

Technetium is a radioactive product of the nuclear fission process. During reprocessing of spent or partially spent fuel from nuclear reactors, the technetium can be released and contaminate other, otherwise good, metals. A specific example is equipment in gaseous diffusion uranium enrichment cascades which have been used to process fuel which was returned from reactors, so-called reactor returns. These returns contained volatile technetium compounds which contaminated the metals in the equipment. Present regulations require that technetium be removed before the metal can be re-used at non-radioactive sites. Removing the technetium from contaminated metals has two desirable results. First, the large amount of nonradioactive metal produced by the process herein described can be recycled at a much lower cost than virgin metal can be produced. Second, large amounts of radioactively contaminated metal can be reduced to relatively small amounts of radioactive slag and large amounts of essentially uncontaminated metal. A new and improved process for removing technetium from iron and other metals is described in which between 1/10 atom % and 5 atom % of manganese is added to the contaminated metal in order to replace the technetium.

Leitnaker, James M.; Trowbridge, Lee D.

1997-12-01T23:59:59.000Z

59

Pentek metal coating removal system: Baseline report  

SciTech Connect

The Pentek coating removal technology was tested and is being evaluated at Florida International University (FIU) as a baseline technology. In conjunction with FIU`s evaluation of efficiency and cost, this report covers evaluation conducted for safety and health issues. It is a commercially available technology and has been used for various projects at locations throughout the country. The Pentek coating removal system consisted of the ROTO-PEEN Scaler, CORNER-CUTTER{reg_sign}, and VAC-PAC{reg_sign}. They are designed to remove coatings from steel, concrete, brick, and wood. The Scaler uses 3M Roto Peen tungsten carbide cutters while the CORNER-CUTTER{reg_sign} uses solid needles for descaling activities. These hand tools are used with the VAC-PAC{reg_sign} vacuum system to capture dust and debris as removal of the coating takes place. The safety and health evaluation during the testing demonstration focused on two main areas of exposure: dust and noise. Dust exposure minimal, but noise exposure was significant. Further testing for each exposure is recommended because of the environment where the testing demonstration took place. It is feasible that the dust and noise levels will be higher in an enclosed operating environment of different construction. In addition, other areas of concern found were arm-hand vibration, whole-body, ergonomics, heat stress, tripping hazards, electrical hazards, machine guarding, and lockout/tagout.

1997-07-31T23:59:59.000Z

60

Electrochemical removal of material from metallic work  

DOE Patents (OSTI)

Deburring, polishing, surface forming and the like are carried out by electrochemical machining with conformable electrode means including an electrically conducting and an insulating web. The surface of the work to be processed is covered by a deformable electrically insulating web or cloth which is perforated and conforms with the work. The web is covered by a deformable perforated electrically conducting screen electrode which also conforms with, and is insulated from, the work by the insulating web. An electrolyte is conducted through the electrode and insulating web and along the work through a perforated elastic member which engages the electrode under pressure pressing the electrode and web against the work. High current under low voltage is conducted betwen the electrode and work through the insulator, removing material from the work. Under the pressure of the elastic member, the electrode and insulator continue to conform with the work and the spacing between the electrode and work is maintained constant.

Csakvary, Tibor (Wilkens Township, Allegheny County, PA); Fromson, Robert E. (Wilkens Township, Allegheny County, PA)

1980-05-13T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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 for producing hydrocarbon fuels and fuel gas from heavy polynuclear hydrocarbons by the use of molten metal halide catalysts  

DOE Patents (OSTI)

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

Gorin, Everett (San Rafael, CA)

1979-01-01T23:59:59.000Z

62

Process for removing cadmium from scrap metal  

DOE Patents (OSTI)

A process for the recovery of a metal, in particular, cadmium contained in scrap, in a stable form. The process comprises the steps of mixing the cadmium-containing scrap with an ammonium carbonate solution, preferably at least a stoichiometric amount of ammonium carbonate, and/or free ammonia, and an oxidizing agent to form a first mixture so that the cadmium will react with the ammonium carbonate to form a water-soluble ammine complex; evaporating the first mixture so that ammine complex dissociates from the first mixture leaving carbonate ions to react with the cadmium and form a second mixture that includes cadmium carbonate; optionally adding water to the second mixture to form a third mixture; adjusting the pH of the third mixture to the acid range whereby the cadmium carbonate will dissolve; and adding at least a stoichiometric amount of sulfide, preferably in the form of hydrogen sulfide or an aqueous ammonium sulfide solution, to the third mixture to precipitate cadmium sulfide. This mixture of sulfide is then preferably digested by heating to facilitate precipitation of large particles of cadmium sulfide. The scrap may be divided by shredding or breaking up to exposure additional surface area. Finally, the precipitated cadmium sulfide can be mixed with glass formers and vitrified for permanent disposal.

Kronberg, J.W.

1994-01-01T23:59:59.000Z

63

Process for removing cadmium from scrap metal  

DOE Patents (OSTI)

A process is described for the recovery of a metal, in particular, cadmium contained in scrap, in a stable form. The process comprises the steps of mixing the cadmium-containing scrap with an ammonium carbonate solution, preferably at least a stoichiometric amount of ammonium carbonate, and/or free ammonia, and an oxidizing agent to form a first mixture so that the cadmium will react with the ammonium carbonate to form a water-soluble ammine complex; evaporating the first mixture so that ammine complex dissociates from the first mixture leaving carbonate ions to react with the cadmium and form a second mixture that includes cadmium carbonate; optionally adding water to the second mixture to form a third mixture; adjusting the pH of the third mixture to the acid range whereby the cadmium carbonate will dissolve; and adding at least a stoichiometric amount of sulfide, preferably in the form of hydrogen sulfide or an aqueous ammonium sulfide solution, to the third mixture to precipitate cadmium sulfide. This mixture of sulfide is then preferably digested by heating to facilitate precipitation of large particles of cadmium sulfide. The scrap may be divided by shredding or breaking up to expose additional surface area. Finally, the precipitated cadmium sulfide can be mixed with glass formers and vitrified for permanent disposal. 2 figures.

Kronberg, J.W.

1995-04-11T23:59:59.000Z

64

Process for removing cadmium from scrap metal  

DOE Patents (OSTI)

A process for the recovery of a metal, in particular, cadmium contained in scrap, in a stable form. The process comprises the steps of mixing the cadmium-containing scrap with an ammonium carbonate solution, preferably at least a stoichiometric amount of ammonium carbonate, and/or free ammonia, and an oxidizing agent to form a first mixture so that the cadmium will react with the ammonium carbonate to form a water-soluble ammine complex; evaporating the first mixture so that ammine complex dissociates from the first mixture leaving carbonate ions to react with the cadmium and form a second mixture that includes cadmium carbonate; optionally adding water to the second mixture to form a third mixture; adjusting the pH of the third mixture to the acid range whereby the cadmium carbonate will dissolve; and adding at least a stoichiometric amount of sulfide, preferably in the form of hydrogen sulfide or an aqueous ammonium sulfide solution, to the third mixture to precipitate cadmium sulfide. This mixture of sulfide is then preferably digested by heating to facilitate precipitation of large particles of cadmium sulfide. The scrap may be divided by shredding or breaking up to expose additional surface area. Finally, the precipitated cadmium sulfide can be mixed with glass formers and vitrified for permanent disposal.

Kronberg, James W. (Aiken, SC)

1995-01-01T23:59:59.000Z

65

Original article Mobility of heavy metals in soil and their uptake  

E-Print Network (OSTI)

Original article Mobility of heavy metals in soil and their uptake by sunflowers grown at different) Abstract - A pot trial was carried out to study the effect of heavy metals on sunflowers (Helianthus annuus L.) grown on three different soils at different levels of heavy metal loading (added in 1987

Recanati, Catherine

66

Metal chelate process to remove pollutants from fluids  

DOE Patents (OSTI)

The present invention relates to improved methods using an organic iron chelate to remove pollutants from fluids, such as flue gas. Specifically, the present invention relates to a process to remove NO[sub x] and optionally SO[sub 2] from a fluid using a metal ion (Fe[sup 2+]) chelate wherein the ligand is a dimercapto compound wherein the --SH groups are attached to adjacent carbon atoms (HS--C--C--SH) or (SH--C--CCSH) and contain a polar functional group so that the ligand of DMC chelate is water soluble. Alternatively, the DMC is covalently attached to a water insoluble substrate such as a polymer or resin, e.g., polystyrene. The chelate is regenerated using electroreduction or a chemical additive. The dimercapto compound bonded to a water insoluble substrate is also useful to lower the concentration or remove hazardous metal ions from an aqueous solution. 26 figures.

Chang, S.G.T.

1994-12-06T23:59:59.000Z

67

Heavy-metal toxicity phenomena in laboratory-scale ANFLOW bioreactors  

DOE Green Energy (OSTI)

An energy-conserving wastewater treatment system was developed based on an anaerobic, upflow (ANFLOW) bioreactor. Since many applications of the ANFLOW process could involve the treatment of wastewaters containing heavy metals, the potentially toxic effects of these metals on the biological processes occurring in ANFLOW columns (primarily acetogenesis and methanogenesis) were investigated. Both step and pulse inputs of zinc ranging from 100 to 1000 mg/L were added to synthetic wastewaters being treated in ANFLOW columns with 0.057-m/sup 3/ volumes. Column responses were used to develop descriptive models for toxicity phenomena in such systems. It was found that an inhibition function could be defined and used to modify a model based on plugflow with axial dispersion and first-order kinetics for soluble substrate removal. The inhibitory effects of zinc on soluble substrate removal were found to be predominantly associated with its sorption by biosolids. Sorption initially occurred in the lower regions of the column, but was gradually observed in higher regions as the sorption capacity of the lower regions was exhausted. Sorption phenomena could be described with the Freundlich equation. Sorption processes were accompanied by shifts of biological processes to regions higher in the columns. A regenerative process was observed when feeding of wastewaters without zinc was resumed. It was postulated that regeneration could be based on sloughing of layers of biofilms, or other biosolids involved in zinc sorption, followed by continued growth of lower layers of biofilms not involved in heavy-metal sorption.

Rivera, A.L.

1982-04-01T23:59:59.000Z

68

Bead and Process for Removing Dissolved Metal Contaminants  

DOE Patents (OSTI)

A bead is provided which comprises or consists essentially of activated carbon immobilized by crosslinked poly (carboxylic acid) binder, sodium silicate binder, or polyamine binder. The bead is effective to remove metal and other ionic contaminants from dilute aqueous solutions. A method of making metal-ion sorbing beads is provided, comprising combining activated carbon, and binder solution (preferably in a pin mixer where it is whipped), forming wet beads, and heating and drying the beads. The binder solution is preferably poly(acrylic acid) and glycerol dissolved in water and the wet beads formed from such binder solution are preferably heated and crosslinked in a convection oven.

Summers, Bobby L., Jr.; Bennett, Karen L.; Foster, Scott A.

2005-01-18T23:59:59.000Z

69

Heavy metals in commercial fish in New Jersey  

SciTech Connect

Levels of contaminants in fish are of particular interest because of the potential risk to humans who consume them. While attention has focused on self-caught fish, most of the fish eaten by the American public comes from commercial sources. We sampled 11 types of fish and shellfish obtained from supermarkets and specialty fish markets in New Jersey and analyzed them for arsenic, cadmium, chromium, lead, manganese, mercury, and selenium. We test the null hypothesis that metal levels do not vary among fish types, and we consider whether the levels of any metals could harm the fish themselves or their predators or pose a health risk for human consumers. There were significant interspecific differences for all metals, and no fish types had the highest levels of more than two metals. There were few significant correlations (Kendall tau) among metals for the three most numerous fish (yellowfin tuna, bluefish, and flounder), the correlations were generally low (below 0.40), and many correlations were negative. Only manganese and lead positively were correlated for tuna, bluefish, and flounder. The levels of most metals were below those known to cause adverse effects in the fish themselves. However, the levels of arsenic, lead, mercury, and selenium in some fish were in the range known to cause some sublethal effects in sensitive predatory birds and mammals and in some fish exceeded health-based standards. The greatest risk from different metals resided in different fish; the species of fish with the highest levels of a given metal sometimes exceeded the human health guidance or standards for that metal. Thus, the risk information given to the public (mainly about mercury) does not present a complete picture. The potential of harm from other metals suggests that people not only should eat smaller quantities of fish known to accumulate mercury but also should eat a diversity of fish to avoid consuming unhealthy quantities of other heavy metals. However, consumers should bear in mind that standards have a margin of safety.

Burger, Joanna [Division of Life Sciences, 604 Allison Road, Piscataway, NJ 08854-8082 (United States) and Environmental and Occupational Health Sciences Institute and Consortium for Risk Evaluation with Stakeholder Participation, Piscataway, NJ 08854 (United States)]. E-mail: burger@biology.rutgers.edu; Gochfeld, Michael [Environmental and Occupational Health Sciences Institute and Consortium for Risk Evaluation with Stakeholder Participation, Piscataway, NJ 08854 (United States); Environmental and Occupational Medicine, UMDNJ-Robert Wood Johnson Medical School, Piscataway, NJ 08854 (United States)

2005-11-15T23:59:59.000Z

70

Magnetic Process For Removing Heavy Metals From Water Employing...  

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

is achieved by flowing the water through a solid magnetized matrix, such as steel wool, such that the magnetite magnetically binds to the solid matrix. The magnetized matrix...

71

Wastewaters at SRS where heavy metals are a potential problem  

SciTech Connect

The principal objective of this report is to identify and prioritize heavy metal-containing wastewaters at the Savannah River Site (SRS) in terms of their suitability for testing of and clean-up by a novel bioremediation process being developed by SRTC. This process involves the use of algal biomass for sequestering heavy metal and radionuclides from wastewaters. Two categories of SRS wastewaters were considered for this investigation: (1) waste sites (primarily non-contained wastes managed by Environmental Restoration), and (2) waste streams (primarily contained wastes managed by Waste Management). An attempt was made to evaluate all sources of both categories of waste throughout the site so that rational decisions could be made with regard to selecting the most appropriate wastewaters for present study and potential future treatment. The investigation included a review of information on surface and/or groundwater associated with all known SRS waste sites, as well as waters associated with all known SRS waste streams. Following the initial review, wastewaters known or suspected to contain potentially problematic concentrations of one or more of the toxic metals were given further consideration.

Wilde, E.W.; Radway, J.C.

1994-11-01T23:59:59.000Z

72

Improved method for removing metal vapor from gas streams  

DOE Patents (OSTI)

This invention relates to a process for gas cleanup to remove one or more metallic contaminants present as vapor. More particularly, the invention relates to a gas cleanup process using mass transfer to control the saturation levels such that essentially no particulates are formed, and the vapor condenses on the gas passage surfaces. It addresses the need to cleanup an inert gas contaminated with cadmium which may escape from the electrochemical processing of Integral Fast Reactor (IFR) fuel in a hot cell. The IFR is a complete, self-contained, sodium-cooled, pool-type fast reactor fueled with a metallic alloy of uranium, plutonium and zirconium, and is equipped with a close-coupled fuel cycle. Tests with a model have shown that removal of cadmium from argon gas is in the order of 99.99%. The invention could also apply to the industrial cleanup of air or other gases contaminated with zinc, lead, or mercury. In addition, the invention has application in the cleanup of other gas systems contaminated with metal vapors which may be toxic or unhealthy.

Ahluwalia, R.K.; Im, K.H.

1994-09-19T23:59:59.000Z

73

Genetic manipulation of a cyanobacterium for heavy metal detoxivication  

DOE Green Energy (OSTI)

Increasing heavy metal contamination of soil and water has produced a need for economical and effective methods to reduce toxic buildup of these materials. Biological systems use metallothionein proteins to sequester such metals as Cu, Cd, and Zn. Studies are underway to genetically engineer a cyanobacteria strain with increased ability for metallothionein production and increased sequestration capacity. Cyanobacteria require only sunlight and CO{sub 2}. Vector constructs are being developed in a naturally competent, unicellular cyanobacterium Anacystis nidulans R2. Closed copies of a yeast copper metallothionein gene have been inserted into a cyanobacterial shuttle vector as well as a vector designed for genomic integration. Transformation studies have produced recombinant cyanobacteria from both of these systems, and work is currently underway to assess the organism`s ability to withstand increasing Cu, Cd, and Zn concentrations.

McCormick, P.; Cannon, G.; Heinhorst, S.

1995-12-31T23:59:59.000Z

74

The Leaching Behavior of Heavy Metals in MSWI Bottom Ash ... - TMS  

Science Conference Proceedings (OSTI)

May 1, 2007 ... The Leaching Behavior of Heavy Metals in MSWI Bottom Ash by Carbonation Reaction with Diffeent Water Content by Nam-Il Um, Kwang-Suk ...

75

Heavy metals processing near-net-forming summary progress report  

SciTech Connect

This study utilized a converging-diverging nozzle to spray-form an alloy having a weight percent composition of 49.6% iron, 49.6% tungsten, and 0.8% carbon into samples for analysis. The alloy was a surrogate that displayed metallurgical characteristics similar to the alloys used in the heavy metals processing industry. US DOE facilities are evaluating advanced technologies which can simplify component fabrication, reduce handling steps, and minimize final machining. The goal of producing net-shaped components can be approached from several directions. In spray forming, molten metal is converted by a nozzle into a plume of fine droplets which quickly cool in flight and solidify against a substrate. The near-final dimension product that is formed receives additional benefits from rapid solidification. This single-step processing approach would aid the heavy metals industry by streamlining fabrication, improving production yields, and minimizing the generation of processing wastes. This Program effort provided a large selection of as-sprayed specimens. These samples were sprayed with gas-to-metal mass ratios ranging from 0.8:1 to 4:1. Samples targeted for analysis were produced from different spray conditions. Metallography on some samples revealed areas that were fully dense and homogeneous at 5,000X. These areas averaged grain sizes of 1 micron diameter. Other samples when viewed at 2,000X were highly segregated in the 10 micron diameter range. Deposit efficiencies of greater than 90% were demonstrated using the untailored spray system. Discharge gases were analyzed and two categories of particles were identified. One category of particle had a chemical composition characteristic of the alloy being sprayed and the second type of particle had a chemical composition characteristic of the ceramics used in the spray system component fabrication. Particles ranged in size from 0.07 to 3 microns in diameter. 8 refs., 67 figs., 20 tabs.

Watson, L.D. [Custom Spray Technologies, Inc., Rigby, ID (United States); Thompson, J.E. [Martin Marietta Energy Systems, Inc., Oak Ridge, TN (United States)

1994-09-01T23:59:59.000Z

76

Trace metals in heavy crude oils and tar sand bitumens  

SciTech Connect

Fe, Ni, and V are considered trace impurities in heavy crude oils and tar sand bitumens. In order to understand the importance of these metals, we have examined several properties: (1) bulk metals levels, (2) distribution in separated fractions, (3) size behavior in feeds and during processing, (4) speciation as a function of size, and (5) correlations with rheological properties. Some of the results of these studies show: (1) V and Ni have roughly bimodal size distributions, (2) groupings were seen based on location, size distribution, and Ni/V ratio of the sample, (3) Fe profiles are distinctively different, having a unimodal distribution with a maximum at relatively large molecular size, (4) Fe concentrations in the tar sand bitumens suggest possible fines solubilization in some cases, (5) SARA separated fractions show possible correlations of metals with asphaltene properties suggesting secondary and tertiary structure interactions, and (6) ICP-MS examination for soluble ultra-trace metal impurities show the possibility of unexpected elements such as U, Th, Mo, and others at concentrations in the ppB to ppM range. 39 refs., 13 figs., 5 tabs.

Reynolds, J.G.

1990-11-28T23:59:59.000Z

77

Comparison of spatial interpolation methods for estimating heavy metals in sediments of Caspian Sea  

Science Conference Proceedings (OSTI)

This study aims to estimate the spatial distribution patterns of six heavy metals: Arsenic (As), Cadmium (Cd), Copper (Cu), Mercury (Hg), Plumbum (Pb), Zinc (Zn) in the sediments of Caspian Sea. Ordinary kriging (OK), genetic algorithm based on artificial ... Keywords: Artificial neural network, Caspian Sea, Fuzzy inference system, Genetic algorithm, Heavy metals, Ordinary kriging, Spatial patterns

S. M. Kazemi; S. M. Hosseini

2011-03-01T23:59:59.000Z

78

Manganese Doping of Magnetic Iron Oxide Nanoparticles: Tailoring Surface Reactivity for a Regenerable Heavy Metal Sorbent  

SciTech Connect

A method for tuning the analyte affinity of magnetic, inorganic nanostructured sorbents for heavy metal contaminants is described. The manganese-doped iron oxide nanoparticle sorbents have a remarkably high affinity compared to the precursor material. Sorbent affinity can be tuned toward an analyte of interest simply by adjustment of the dopant quantity. The results show that following the Mn doping process there is a large increase in affinity and capacity for heavy metals (i.e., Co, Ni, Zn, As, Ag, Cd, Hg, and Tl). Capacity measurements were carried out for the removal of cadmium from river water and showed significantly higher loading than the relevant commercial sorbents tested for comparison. The reduction in Cd concentration from 100 ppb spiked river water to 1 ppb (less than the EPA drinking water limit of 5 ppb for Cd) was achieved following treatment with the Mn-doped iron oxide nanoparticles. The Mn-doped iron oxide nanoparticles were able to load 1 ppm of Cd followed by complete stripping and recovery of the Cd with a mild acid wash. The Cd loading and stripping is shown to be consistent through multiple cycles with no loss of sorbent performance.

Warner, Cynthia L.; Chouyyok, Wilaiwan; Mackie, Katherine E.; Neiner, Doinita; Saraf, Laxmikant; Droubay, Timothy C.; Warner, Marvin G.; Addleman, Raymond S.

2012-02-28T23:59:59.000Z

79

Experimental investigation and thermodynamic modeling of extraction of heavy metal ions from aqueous solutions by chelation in supercritical carbon dioxide  

E-Print Network (OSTI)

Wastewater streams containing heavy metals are common in industry. To prevent the contamination of clean water sources, the Clean Water Act specifies limits on the heavy metal concentrations of industrial waste water. This creates a strong need for developing cost effective and environmentally friendly metal removal technologies. Solvent extraction has been recognized as one of the best methods for removing metals from wastewater. Although the metals are easily removed, this process has two major disadvantages. First, the solvent/metal solution must be subsequently purified. Second, since the solvent may be miscible in the aqueous phase, the residual solvent must be removed from the water stream. These disadvantages can be eliminated by substituting conventional organic solvents with supercritical fluids. The main objective of this research has been to investigate the potential and feasibility of heavy metal ion extraction through chelation in supercritical CO2. Copper has been chosen as the model contaminant as it is frequently found in industrial waste streams. Different chelating agents have been tested to find the most appropriate one for copper. Analytical methods have been developed to quantify supercritical and aqueous phase compositions. Specifically, an Atomic Absorption Analyzer and a Gas Chromatograph have been employed. Copper ions have been successfully extracted up to 97% on different isotherms. Considering the phase equilibria and the thirteen reactions taking place in the system, a thermodynamic model has been developed. This model predicts the system pH which is a important factor in design of metal extraction units. With the model the efficiency of the extraction with different chelating agents at different temperatures and pressures is easily estimated. The model is also capable of calculating the concentrations of chemical species present in the system. This study proposed a novel and viable technique for the remediation of metal ions in waste water streams. In conjunction with the developed model the efficiency of this process for a specific industrial application can be accurately estimated. The results of this study demonstrate that this process is both environmentally friendly and economically feasible for wide spread industrial use.

Uyansoy, Hakki

1995-01-01T23:59:59.000Z

80

Treatability studies and large-scale treatment of aqueous mixed waste containing heavy metals  

SciTech Connect

Wastes have accumulated at the Idaho National Engineering Laboratory through routine laboratory practices, experimental engineering operations, and decommissioning and decontamination of nuclear reactor facilities. A storage tank at the Test Area North held approximately 129,000 L of acidic wastewater and contained prohibited levels of lead and mercury. Radioactive constituents were also present; the most predominant being radiocesium Cs-137 and radiocobalt Co-60. Bench-scale studio were undertaken to evaluate ion exchange as a means of removing the contaminants. A set of breakthrough curves was obtained and identified capacity constraints, selectivities, and operating requirements of candidate resins. Treatment studies indicated that Purolite S-920 resin could effectively remove mercury, while Rohm and Haas` Amberlite 200-CH was used for lead and radionuclide removal. Based on these laboratory tests a full-scale facility, using multiple ion exchange columns, was designed and operated in the spring of 1994. The liquid effluents were discharged to an onsite evaporation pond and met RCRA disposal limits for hazardous metals and self-imposed radionuclide limits. All secondary wastes and residues were sampled and subjected to the to)dc characteristic leaching procedure. The resulting leachate concentrations were below RCRA discharge limits and, therefore, these will be disposed of at the onsite low-level disposal facility. After concluding the tank wastewater operations, enough reserve resin capacity was available to treat three additional mixed wastes residing onsite. These totaled about 1,900 L (500 gal) and contained prohibited levels of chromium, cadmium, and barium. Laboratory studies demonstrated that these heavy metals could also be removed by the existing resins. Treatment was performed at the full-scale facility with the effluents discharged to the evaporation pond.

Haefner, D.R.

1995-12-01T23:59:59.000Z

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81

Composites for removing metals and volatile organic compounds and method thereof  

DOE Patents (OSTI)

Functionalized hydrophobic aerogel/solid support structure composites have been developed to remove metals and organic compounds from aqueous and vapor media. The targeted metals and organics are removed by passing the aqueous or vapor phase through the composite which can be in molded, granular, or powder form. The composites adsorb the metals and the organics leaving a purified aqueous or vapor stream. The species-specific adsorption occurs through specific functionalization of the aerogels tailored towards specific metals and/or organics. After adsorption, the composites can be disposed of or the targeted metals and/or organics can be reclaimed or removed and the composites recycled.

Coronado, Paul R. (Livermore, CA); Coleman, Sabre J. (Oakland, CA); Reynolds, John G. (San Ramon, CA)

2006-12-12T23:59:59.000Z

82

Immobilization of heavy metals by calcium sulfoaluminate cement  

Science Conference Proceedings (OSTI)

Two types of calcium sulfoaluminate cement containing 20% and 30% phosphogypsum, respectively, were investigated for their ability in hazardous waste stabilization. Fourteen series of pastes were prepared, each containing the following soluble salt: Na{sub 2}CrO{sub 4}.4H{sub 2}O; Na{sub 2}Cr{sub 2}O{sub 7}.2H{sub 2}O; CrCl{sub 3}.6H{sub 2}O; Pb(NO{sub 3}){sub 2}; Zn(NO{sub 3}){sub 2}.6H{sub 2}O; ZnSO{sub 4}.7H{sub 2}O; and CdCl{sub 2}.5H2O. The level of pollution was 0.069 mol of heavy metal per Kg of cement. The study has been carried out by means of X-ray diffraction, thermal analysis, scanning electron microscopy, mercury intrusion porosimetry, electrical conductivity, and leaching tests. Very good retention of lead, cadmium, zinc and trivalent chromium is observed. The retention of hexavalent chromium depends upon the nature of the binder: the cement containing 20% gypsum develops the best behaviour. This is explained by the microstructure of the hydrated paste: in the paste containing 30% gypsum, delayed ettringite precipitates and damages the hardened paste.

Peysson, S. [Unite de Recherche en Genie Civil-MATERIAUX, Institut National des Sciences Appliquees de Lyon, Domaine Scientifique de la Doua, Batiment J. Tuset, 12, Avenue des Arts, 69 621 Villeurbanne Cedex (France); Pera, J. [Unite de Recherche en Genie Civil-MATERIAUX, Institut National des Sciences Appliquees de Lyon, Domaine Scientifique de la Doua, Batiment J. Tuset, 12, Avenue des Arts, 69 621 Villeurbanne Cedex (France)]. E-mail: Jean.Pera@insa-lyon.fr; Chabannet, M. [Unite de Recherche en Genie Civil-MATERIAUX, Institut National des Sciences Appliquees de Lyon, Domaine Scientifique de la Doua, Batiment J. Tuset, 12, Avenue des Arts, 69 621 Villeurbanne Cedex (France)

2005-12-15T23:59:59.000Z

83

Process for sodium sulfide/ferrous sulfate treatment of hexavalent chromium and other heavy metals  

SciTech Connect

433 of 9384 ) United States Patent 5,000,859 Suciu ,   et al. March 19, 1991 Process for sodium sulfide/ferrous sulfate treatment of hexavalent chromium and other heavy metals

Suciu, Dan F. (Idaho Falls, ID); Wikoff, Penny M. (Idaho Falls, ID); Beller, John M. (Idaho Falls, ID); Carpenter, Charles J. (Lynn Haven, FL)

1991-01-01T23:59:59.000Z

84

Fiber optic/cone penetrometer system for subsurface heavy metals detection  

Science Conference Proceedings (OSTI)

This document describes a project designed to develop an intergrated fiber optic sensor/cone penetrometer system to analyze the heavy metals content of the subsurface as a site characterization tool.

Saggese, S.; Greenwell, R.

1995-12-01T23:59:59.000Z

85

Effects of residues from municipal solid waste landfill on corn yield and heavy metal content  

Science Conference Proceedings (OSTI)

The effects of residues from municipal solid waste landfill, Khon Kaen Municipality, Thailand, on corn (Zea mays L.) yield and heavy metal content were studied. Field experiments with randomized complete block design with five treatments (0, 20, 40, 60 and 80% v/v of residues and soil) and four replications were carried out. Corn yield and heavy metal contents in corn grain were analyzed. Corn yield increased by 50, 72, 85 and 71% at 20, 40, 60 and 80% treatments as compared to the control, respectively. All heavy metals content, except cadmium, nickel and zinc, in corn grain were not significantly different from the control. Arsenic, cadmium and zinc in corn grain were strongly positively correlated with concentrations in soil. The heavy metal content in corn grain was within regulated limits for human consumption.

Prabpai, S. [Suphan Buri Campus Establishment Project, Kasetsart University, 50 U Floor, Administrative Building, Paholyothin Road, Jatujak, Bangkok 10900 (Thailand)], E-mail: s.prabpai@hotmail.com; Charerntanyarak, L. [Department of Epidemiology, Faculty of Public Health, Khon Kaen University, Khon Kaen 40002 (Thailand)], E-mail: lertchai@kku.ac.th; Siri, B. [Department of Agronomy, Faculty of Agriculture, Khon Kaen University, Khon Kaen 40002 (Thailand)], E-mail: boonmee@kku.ac.th; Moore, M.R. [The University of Queensland, The National Research Center for Environmental Toxicology, 39 Kessels Road, Coopers Plans, Brisbane, Queensland 4108 (Australia)], E-mail: m.moore@uq.edu.au; Noller, Barry N. [The University of Queensland, Centre for Mined Land Rehabilitation, Brisbane, Queensland 4072 (Australia)], E-mail: b.noller@uq.edu.au

2009-08-15T23:59:59.000Z

86

Heavy metals in bullfrog (Rana catesbeiana) tadpoles: Effects of depuration before analysis  

SciTech Connect

Although tadpoles may well be excellent organisms to use as bioindicators of heavy metal contamination, the relationship of deposition in the body compared to the tail, and the effect of sediments or other debris in the digestive tract on heavy metal concentrations is unknown. The authors examined the effect of experimental depuration of bullfrog (Rana catesbeiana) tadpoles on heavy metal and selenium concentrations in intact tadpoles, as well as their bodies and tails. They defined depuration in this experiment as allowing defecation as an elimination process for intestinal contents. The authors maintained wild-caught tadpoles in clean water for 0, 24, 48, and 72 h to determine the effects of clearing on heavy metal concentrations. They also examined the concentrations of heavy metals in the whole body and digestive tract separately. The authors test the null hypotheses that no differences occur in metals as a function of time in uncontaminated water, and that no differences occur in metal concentrations in the body compared to the tail and to the digestive tract. They rejected these hypotheses based on regression models. Variance in concentrations of chromium (77%) and lead (70%) were explained by part and clearing time; for manganese (80%), mercury (64%), selenium (28%), and cadmium (25%) the variation was explained only by body part; for arsenic (53%), the variation was explained by part, clearing time, and weight of the various parts. For those metals in which clearing time explained part of the variation, metal concentrations in both the body and tail decreased after 24 and 48 h, but increased slightly thereafter. Clearing, however, did not greatly decrease metal concentrations in either the body or tail. These data suggest that for some metals (mercury, manganese, cadmium, selenium), clearing has no effect, and for others the effect is slight. For fresh tadpoles, however, the digestive tract contained significantly higher concentrations of all metals than either the body or head, probably reflecting metals absorbed to sediment particles in the gut.

Burger, J. [Rutgers Univ., Piscataway, NJ (United States); Snodgrass, J. [Rutgers Univ., Piscataway, NJ (United States)]|[Savannah River Ecology Lab., Aiken, SC (United States)

1998-11-01T23:59:59.000Z

87

Method for removal of metal atoms from aqueous solution using suspended plant cells  

DOE Patents (OSTI)

The use of plant suspension cultures to remove ionic metallic species and TNT-based explosives and their oxidation products from aqueous solution is described. Several plant strains were investigated including D. innoxia, Citrus citrus, and Black Mexican Sweet Corn. All showed significant ability to remove metal ions. Ions removed to sub-ppm levels include barium, iron, and plutonium. D. innoxia cells growing in media containing weapons effluent contaminated with Ba.sup.2+ also remove TNT, other explosives and oxidation products thereof from solution. The use of dead, dehydrated cells were also found to be of use in treating waste directly.

Jackson, Paul J. (Los Alamos, NM); Torres, deceased, Agapito P. (late of Los Alamos, NM); Delhaize, Emmanuel (Kaleen, AU)

1992-01-01T23:59:59.000Z

88

Leachability of heavy metals from growth media containing source-separated municipal solid waste compost  

Science Conference Proceedings (OSTI)

The leaching of heavy metals in source-separated municipal solid waste (MSW) compost was determined by irrigation leaching of growth medium, admixed with varying amounts of compost, used for container grown plants. Perennial flowers (black-eyed Susan, Rudbeckia hirta L.) were grown in 2-L containers filled with the growth medium for a 10-wk period. Rainfall was supplemented with overhead irrigation to supply 2 cm of water per day. Leachates collected over each 2-wk period were analyzed for Cd, Cr, Cu, Ni, Pb, and Zn using atomic spectrometry. Concentrations of the heavy metals in the leachates increased with increasing proportions of MSW compost in the growth medium, but decreased with time of leaching. Leaching of the metals occurred at relatively high concentrations initially, followed by continued leaching at low concentrations. The initial leaching of heavy metals is attributed to their soluble or exchangeable forms and the subsequent slow leaching to the solid compounds. The concentrations of the heavy metals remained below the current drinking water standards in all treatments throughout the leaching period. The results thus suggest that contamination of groundwater with heavy metals from source-separated MSW compost applied as a soil amendment should be negligible, as the low concentrations in the leachates leaving the surface soil would be further attenuated by the subsoil. 29 refs., 6 figs., 1 tab.

Sawhney, B.L.; Bugbee, G.J.; Stilwell, D.E. [Connecticut Agricultural Experimental Station, New Haven, CT (United States)

1994-07-01T23:59:59.000Z

89

Pentek metal coating removal system: Baseline report; Greenbook (chapter)  

SciTech Connect

The Pentek coating removal technology was tested and is being evaluated at Florida International University (FIU) as a baseline technology. In conjunction with FIU`s evaluation of efficiency and cost, this report covers evaluation conducted for safety and health issues. It is a commercially available technology and has been used for various projects at locations throughout the country. The Pentek coating removal system consisted of the ROTO-PEEN Scaler, CORNER-CUTTER{reg_sign}, and VAC-PAC{reg_sign}. They are designed to remove coatings from steel, concrete, brick, and wood. The Scaler uses 3M Roto Peen tungsten carbide cutters while the CORNER-CUTTER{reg_sign} uses solid needles for descaling activities. These hand tools are used with the VAC-PAC{reg_sign} vacuum system to capture dust and debris as removal of the coating takes place. The safety and health evaluation during the testing demonstration focused on two main areas of exposure: dust and noise. Dust exposure minimal, but noise exposure was significant. Further testing for each exposure is recommended because of the environment where the testing demonstration took place. It is feasible that the dust and noise levels will be higher in an enclosed operating environment of different construction. In addition, other areas of concern found were arm-hand vibration, whole-body, ergonomics, heat stress, tripping hazards, electrical hazards, machine guarding, and lockout/tagout.

1997-07-31T23:59:59.000Z

90

Method of removing bulk sodium from metallic surfaces  

DOE Patents (OSTI)

A process of removing sodium from an article, particularly one made of stainless steel, by treating it with a mixture of water vapor and a gas which is inert to sodium is described. By selecting combinations of temperature and water vapor-to-gas ratio, the reaction temperature is controlled to prevent damage to the articles.

Maffei, H.P.; Borisch, R.R.

1975-11-11T23:59:59.000Z

91

Heavy metals in liquid pig manure in light of bacterial antimicrobial resistance  

Science Conference Proceedings (OSTI)

Heavy metals are regularly found in liquid pig manure, and might interact with bacterial antimicrobial resistance. Concentrations of heavy metals were determined by atomic spectroscopic methods in 305 pig manure samples and were connected to the phenotypic resistance of Escherichia coli (n=613) against 29 antimicrobial drugs. Concentrations of heavy metals (/kg dry matter) were 0.08-5.30 mg cadmium, 1.1-32.0 mg chrome, 22.4-3387.6 mg copper, doxycycline were also demonstrated in a laboratory trial. Antimicrobial resistance in the porcine microflora might be increased by copper and zinc. By contrast, the occurrence of mercury in the environment might, due to co-toxicity, act counter-selective against antimicrobial resistant strains.

Hoelzel, Christina S., E-mail: Christina.Hoelzel@wzw.tum.de [Chair of Animal Hygiene, Technische Universitaet Muenchen, Weihenstephaner Berg 3, 85354 Freising (Germany); Mueller, Christa [Institute for Agroecology, Organic Farming and Soil Protection, Bavarian State Research Center for Agriculture (LfL), Lange Point 12, 85354 Freising (Germany)] [Institute for Agroecology, Organic Farming and Soil Protection, Bavarian State Research Center for Agriculture (LfL), Lange Point 12, 85354 Freising (Germany); Harms, Katrin S. [Chair of Animal Hygiene, Technische Universitaet Muenchen, Weihenstephaner Berg 3, 85354 Freising (Germany)] [Chair of Animal Hygiene, Technische Universitaet Muenchen, Weihenstephaner Berg 3, 85354 Freising (Germany); Mikolajewski, Sabine [Department for Quality Assurance and Analytics, Bavarian State Research Center for Agriculture (LfL), Lange Point 4, 85354 Freising (Germany)] [Department for Quality Assurance and Analytics, Bavarian State Research Center for Agriculture (LfL), Lange Point 4, 85354 Freising (Germany); Schaefer, Stefanie; Schwaiger, Karin; Bauer, Johann [Chair of Animal Hygiene, Technische Universitaet Muenchen, Weihenstephaner Berg 3, 85354 Freising (Germany)] [Chair of Animal Hygiene, Technische Universitaet Muenchen, Weihenstephaner Berg 3, 85354 Freising (Germany)

2012-02-15T23:59:59.000Z

92

REVIEW ARTICLE FOCUS Quantum criticality in heavy-fermion metals  

E-Print Network (OSTI)

again1 . The transformation between ice and water also illustrates another concept in phase transitions the collective fluctuations of matter undergoing a second-order phase transition at zero temperature. Heavy a quantum phase transition to a new ground state. As simple as this sounds, quantum phase transitions

Loss, Daniel

93

Biosorption of heavy metal ions to brown algae, Macrocystis pyrifera, Kjellmaniella crassiforia, and Undaria pinnatifida  

SciTech Connect

A fundamental study of the application of brown algae to the aqueous-phase separation of toxic heavy metals was carried out. The biosorption characteristics of cadmium and lead ions were determined with brown algae, Macrocystis pyrifera, Kjellmaniella crassiforia, and Undaria pinnatifida. A metal binding model proposed by the authors was used for the description of metal binding data. The results showed that the biosorption of bivalent metal ions to brown algae was due to bivalent binding to carboxylic groups on alginic acid in brown algae.

Seki, Hideshi; Suzuki, Akira [Hokkaido Univ., Hakodate (Japan)

1998-10-01T23:59:59.000Z

94

Cone Penetrometer for Subsurface Heavy Metals Detection. Semiannual report, November 1, 1996--March 31, 1997  

Science Conference Proceedings (OSTI)

Surface and subsurface contamination of soils by heavy metals, including Pb, Cr, Cu, Zn, and Cd, has become an area of concern for many industrial and government organizations (1). Conventional sampling and analysis techniques for soil provide a high degree of sensitivity and selectivity for individual analytes. However, obtaining a representative sampling and analysis from a particular site using conventional techniques is time consuming and costly (2). Additionally, conventional methods are difficult to implement in the field for in situ and/or real-time applications. Therefore, there is a need for characterization and monitoring techniques for heavy metals in soils which allow cost-effective, rapid, in situ measurements. Laser-induced breakdown spectroscopy (LIBS) has been used to successfully measure metals content in a variety of matrices (3-15) including soil (16,17). Under the Department of Energy (DOE) Federal Energy Technology Center (FETC) Industry Program, Science {ampersand} Engineering Associates (SEA) is developing a subsurface cone penetrometer (CPT) probe for heavy metals detection that employs LIBS (18). The LIES-CPT unit is to be applied to in situ, real-time sampling and analysis of heavy metals in soil. As part of its contract with DOE FETC, SEA is scheduled to field test its LIBS-CPT system in September 1997.

Grisanti, Ames A.; Timpe, Ronald C.; Foster, H.J.; Eylands, Kurt E.; Crocker, Charlene R.

1997-12-31T23:59:59.000Z

95

Plasma treatment of INEL soil contaminated with heavy metals  

Science Conference Proceedings (OSTI)

INEL soil spiked with inorganic salts of chromium, lead, mercury, silver, and zinc was melted in a 150 kW plasma furnace to produce a glassy slag product. This glassy slag is an environmentally safe waste form. In order to reduce the melting temperature of the soil, sodium carbonate was added to half of the test batches. Random sample from each batch of glassy slag product were analyzed by an independent laboratory for total metals concentration and leachability of metals via the Environmental Protection Agency (EPA) toxicity characterization leaching procedure (RCLP) tests. These tests showed the residual metals were very tightly bound to the slag matrix and were within EPA TCLP limits under these test conditions. Additionally, scanning electron microscopy (SEM) and emissions dispersive spectroscopy (EDS) analysis of the vitrified soil also confirmed that the added metals present in the vitrified soil were totally contained in the crystalline phase as distinct oxide crystallites.

Detering, B.A.; Batdorf, J.A.

1992-01-01T23:59:59.000Z

96

Fluid clathrate system for continuous removal of heavy noble gases from mixtures of lighter gases  

DOE Patents (OSTI)

An apparatus and method for separation of heavy noble gas in a gas volume. An apparatus and method have been devised which includes a reservoir containing an oil exhibiting a clathrate effect for heavy noble gases with a reservoir input port and the reservoir is designed to enable the input gas volume to bubble through the oil with the heavy noble gas being absorbed by the oil exhibiting a clathrate effect. The gas having reduced amounts of heavy noble gas is output from the oil reservoir, and the oil having absorbed heavy noble gas can be treated by mechanical agitation and/or heating to desorb the heavy noble gas for analysis and/or containment and allow recycling of the oil to the reservoir.

Gross, Kenneth C. (Bolingbrook, IL); Markun, Francis (Joliet, IL); Zawadzki, Mary T. (South Bend, IN)

1998-01-01T23:59:59.000Z

97

Fluid clathrate system for continuous removal of heavy noble gases from mixtures of lighter gases  

DOE Patents (OSTI)

An apparatus and method are disclosed for separation of heavy noble gas in a gas volume. An apparatus and method have been devised which includes a reservoir containing an oil exhibiting a clathrate effect for heavy noble gases with a reservoir input port and the reservoir is designed to enable the input gas volume to bubble through the oil with the heavy noble gas being absorbed by the oil exhibiting a clathrate effect. The gas having reduced amounts of heavy noble gas is output from the oil reservoir, and the oil having absorbed heavy noble gas can be treated by mechanical agitation and/or heating to desorb the heavy noble gas for analysis and/or containment and allow recycling of the oil to the reservoir. 6 figs.

Gross, K.C.; Markun, F.; Zawadzki, M.T.

1998-04-28T23:59:59.000Z

98

Analysis of removal alternatives for the Heavy Water Components Test Reactor at the Savannah River Site. Revision 1  

SciTech Connect

This engineering study evaluates different alternatives for decontamination and decommissioning of the Heavy Water Components Test Reactor (HWCTR). Cooled and moderated with pressurized heavy water, this uranium-fueled nuclear reactor was designed to test fuel assemblies for heavy water power reactors. It was operated for this purpose from march of 1962 until December of 1964. Four alternatives studied in detail include: (1) dismantlement, in which all radioactive and hazardous contaminants would be removed, the containment dome dismantled and the property restored to a condition similar to its original preconstruction state; (2) partial dismantlement and interim safe storage, where radioactive equipment except for the reactor vessel and steam generators would be removed, along with hazardous materials, and the building sealed with remote monitoring equipment in place to permit limited inspections at five-year intervals; (3) conversion for beneficial reuse, in which most radioactive equipment and hazardous materials would be removed and the containment building converted to another use such as a storage facility for radioactive materials, and (4) entombment, which involves removing hazardous materials, filling the below-ground structure with concrete, removing the containment dome and pouring a concrete cap on the tomb. Also considered was safe storage, but this approach, which has, in effect, been followed for the past 30 years, did not warrant detailed evaluation. The four other alternatives were evaluate, taking into account factors such as potential effects on the environment, risks, effectiveness, ease of implementation and cost. The preferred alternative was determined to be dismantlement. This approach is recommended because it ranks highest in the comparative analysis, would serve as the best prototype for the site reactor decommissioning program and would be most compatible with site property reuse plans for the future.

Owen, M.B.

1997-04-01T23:59:59.000Z

99

Proceedings of Soil Decon `93: Technology targeting radionuclides and heavy metals  

SciTech Connect

The principal objective for convening this workshop was to exchange ideas and discuss with scientists and engineers methods for removing radionuclides and/or toxic metals from soils. Over the years there have been numerous symposia, conferences, and workshops directed at soil remediation. However, this may be the first where the scope was narrowed to the removal of radionuclides and toxic metals from soils. The intent was to focus on the separation processes controlling the removal of the radionuclide and/or metal from soil. Its purpose was not intended to be a soil washing/leaching workshop, but rather to identify a variety or combination of processes (chemical, physical, and biological) that can be used in concert with the applicable engineering approaches to decontaminate soils of radionuclides and toxic metals. Abstracts and visual aids used by the speakers of the workshop are presented in this document.

1993-09-01T23:59:59.000Z

100

A fuzzy logic based system for heavy metals loaded wastewaters monitoring  

Science Conference Proceedings (OSTI)

The paper presents a fuzzy logic based system for wastewater quality monitoring with the purpose of attenuating the environmental impact of the heavy metals loaded wastewaters. The proposed method offers an improvement over the traditionally modelling ... Keywords: environmental indices, fuzzy logic, fuzzy rules, wastewater quality monitoring

Daniel Dunea; Mihaela Oprea

2010-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Using alternative chemicals in the flotation of heavy metals from lead mill tailings  

Science Conference Proceedings (OSTI)

The U.S. Bureau of Mines (USBM) investigated alternative chemicals for the flotation of heavy metal values from southeast Missouri lead mill tailings. The objectives of the study were to lower the Pb remaining in the reprocessed tailings to canola oil, to be as effective as classic sulfide flotation reagents.

Benn, F.W. [Bureau of Mines, Rolla, MO (United States)

1995-04-01T23:59:59.000Z

102

CO2 Removal from Flue Gas Using MIcroporous Metal Organic Frameworks  

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

Removal from Flue Gas Using Removal from Flue Gas Using Microporous Metal Organic Frameworks Background The mission of the U.S. Department of Energy's (DOE) Existing Plants, Emissions, & Capture (EPEC) Research & Development (R&D) Program is to develop innovative environmental control technologies to enable full use of the nation's vast coal reserves, while at the same time allowing the current fleet of coal-fired power plants to comply with existing and emerging environmental regulations. The EPEC R&D

103

Life Cycle Based Greenhouse Gas Footprints of Metal Production ...  

Science Conference Proceedings (OSTI)

The Removal of Heavy Metals and Upgrading Crude Bio-oil from Pteris Vittata Stems and Leaves Harvest Using Hydrothermal Upgrading Process ...

104

Comparison of methods for leaching heavy metals from composts  

SciTech Connect

This paper presents the determination of total iron, copper, zinc, chromium, nickel, lead, cadmium and mercury contents in the compost obtained from sorted municipal organic solid waste applying the following methods of sample mineralization: 40% hydrofluoric acid with preliminary incineration of a sample, a mixture of concentrated nitric(V) and chloric(VII) acids with preliminary incineration of organic matter and a mixture of nitric(V) and chloric(VII) acids without sample incineration. The speciation analysis of Tessier was used to estimate the bioavailability of the metals. Elution degrees of the mobile forms of the metals from the compost with 10% nitric(V) acid and 1 mol/dm{sup 3} hydrochloric acid were compared. The contents of the elements in the eluates were determined applying atomic absorption spectrometry.

Ciba, Jerzy; Zolotajkin, Maria; Kluczka, Joanna; Loska, Krzysztof; Cebula, Jan

2003-07-01T23:59:59.000Z

105

Means for obtaining a metal ion beam from a heavy-ion cyclotron source  

DOE Patents (OSTI)

A description is given of a modification to a cyclotron ion source used in producing a high intensity metal ion beam. A small amount of an inert support gas maintains the usual plasma arc, except that it is necessary for the support gas to have a heavy mass, e.g., xenon or krypton as opposed to neon. A plate, fabricated from the metal (or anything that can be sputtered) to be ionized, is mounted on the back wall of the ion source arc chamber and is bombarded by returning energetic low-charged gas ions that fail to cross the initial accelerating gap between the ion source and the accelerating electrode. Some of the atoms that are dislodged from the plate by the returning gas ions become ionized and are extracted as a useful beam of heavy ions. (auth)

Hudson, E.D.; Mallory, M.L.

1975-08-01T23:59:59.000Z

106

Fixation and partitioning of heavy metals in slag after incineration of sewage sludge  

Science Conference Proceedings (OSTI)

Highlights: Black-Right-Pointing-Pointer The contents and partitioning of HMs in slag of sludge incineration were examined. Black-Right-Pointing-Pointer The fixation rate decreases with residential time and finally keeps a constant. Black-Right-Pointing-Pointer Water mass fraction of 55% is optimal for the sediment for Ni, Mn, Zn, Cu and Cr. Black-Right-Pointing-Pointer Water mass fraction of 75% is optimal for the sediment for Pb. Black-Right-Pointing-Pointer We found higher temperature versus lower non-residual fraction except that of Pb. - Abstract: Fixation of heavy metals in the slag produced during incineration of sewage sludge will reduce emission of the metals to the atmosphere and make the incineration process more environmentally friendly. The effects of incineration conditions (incineration temperature 500-1100 Degree-Sign C, furnace residence time 0-60 min, mass fraction of water in the sludge 0-75%) on the fixation rates and species partitioning of Cd, Pb, Cr, Cu, Zn, Mn and Ni in slag were investigated. When the incineration temperature was increased from 500 to 1100 Degree-Sign C, the fixation rate of Cd decreased from 87% to 49%, while the fixation rates of Cu and Mn were stable. The maximum fixation rates for Pb and Zn and for Ni and Cr were reached at 900 and 1100 Degree-Sign C, respectively. The fixation rates of Cu, Ni, Cd, Cr and Zn decreased as the residence time increased. With a 20 min residence time, the fixation rates of Pb and Mn were low. The maximum fixation rates of Ni, Mn, Zn, Cu and Cr were achieved when the mass fraction of water in the sludge was 55%. The fixation rate of Cd decreased as the water mass fraction increased, while the fixation rate of Pb increased. Partitioning analysis of the metals contained in the slag showed that increasing the incineration temperature and residence time promoted complete oxidation of the metals. This reduced the non-residual fractions of the metals, which would lower the bioavailability of the metals. The mass fraction of water in the sludge had little effect on the partitioning of the metals. Correlation analysis indicated that the fixation rates of heavy metals in the sludge and the forms of heavy metals in the incinerator slag could be controlled by optimization of the incineration conditions. These results show how the bioavailability of the metals can be reduced for environmentally friendly disposal of the incinerator slag.

Chen Tao [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Graduate School of Chinese Academy of Sciences, Beijing 100082 (China); Yan Bo, E-mail: yanbo2007@gig.ac.cn [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China)

2012-05-15T23:59:59.000Z

107

A Novel Sorbent-Based Process for High Temperature Trace Metals...  

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

Sorbent-Based Process for High Temperature Trace Metals Removal from Coal-Derived Syngas Description Gasification converts coal and other heavy feedstocks into synthesis gas...

108

Mercury Removal from Aqueous Systems Using Commercial and Laboratory Prepared Metal Oxide Nanoparticles  

E-Print Network (OSTI)

Five commercial metal oxide nanoparticles (CuO, SiO2, Fe2O3, TiO2 and Al2O3) have been individually screened for mercury removal in a batch reactor under bicarbonate buffered and non-buffered aqueous solutions (DI water). Copper oxide was then selected for surface modification to enhance mercury removal. The surfaces of both laboratory prepared and commercially available copper oxide nanoparticles were treated with 1-octanethiol to produce copper sulfide and/or copper alkanethiol nanoparticles. The resulting particles were characterized using X-Ray Fluorescence(XRF), X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The novel nanoparticles demonstrated very high mercury removal (> 99%) from both the buffered and non-buffered aqueous solutions.

Desai, Ishan

2009-08-01T23:59:59.000Z

109

Sources of heavy metal contamination in Swedish wood waste used for combustion  

SciTech Connect

In this paper, wood waste (RWW) recovered for heat production in Sweden was studied. Previous research has concluded that RWW contains elevated amounts of heavy metals, causing environmental problems during waste management. This study extends previous work on RWW by analysing which pollution sources cause this contamination. Using existing data on the metal contents in various materials, and the amounts of these materials in RWW, the share of the elevated amounts of metals in RWW that these materials explain was quantified. Six different materials occurring in RWW were studied and the results show that they explain from 70% to 100% of the amounts of arsenic, chromium, lead, copper and zinc in RWW. The most important materials contributing to contamination of RWW are surface-treated wood, industrial preservative-treated wood, plastic and galvanised fastening systems. These findings enable the development and evaluation of strategies aiming to decrease pollution and resource loss from handling RWW. It is argued that source separation and measures taken further downstream from the generation site, such as treatment, need to be combined to substantially decrease the amount of heavy metals in RWW.

Krook, J. [Department of Mechanical Engineering, Linkoeping University, SE-581 83 Linkoeping (Sweden)]. E-mail: joakr@ikp.liu.se; Martensson, A. [Department of Mechanical Engineering, Linkoeping University, SE-581 83 Linkoeping (Sweden); Eklund, M. [Department of Mechanical Engineering, Linkoeping University, SE-581 83 Linkoeping (Sweden)

2006-07-01T23:59:59.000Z

110

Heavy Metal Immobilization Through Phosphate and Thermal Treatment of Dredged Sediments  

Science Conference Proceedings (OSTI)

Disposal of dredged sediments is expensive and poses a major challenge for harbor dredging projects. Therefore beneficial reuse of these sediments as construction material is highly desirable assuming contaminants such as heavy metals are immobilized and organics are mineralized. In this research, the effect of the addition of 2.5% phosphate, followed by thermal treatment at 700 C, was investigated for metal contaminants in dredged sediments. Specifically, Zn speciation was evaluated, using X-ray absorption spectroscopy (XAS), by applying principal component analysis (PCA), target transformation (TT), and linear combination fit (LCF) to identify the main phases and their combination from an array of reference compounds. In dredged sediments, Zn was present as smithsonite (67%) and adsorbed to hydrous manganese oxides (18%) and hydrous iron oxides (15%). Phosphate addition resulted in precipitation of hopeite (22%), while calcination induced formation of spinels, gahnite (44%), and franklinite (34%). Although calcination was previously used to agglomerate phosphate phases by sintering, we found that it formed sparingly soluble Zn phases. Results from the U.S. EPA toxicity characteristic leaching procedure (TCLP) confirmed both phosphate addition and calcination reduced leachability of heavy metals with the combined treatment achieving up to an 89% reduction.

Ndiba,P.; Axe, L.; Boonfueng, T.

2008-01-01T23:59:59.000Z

111

Method and apparatus for removal of gaseous, liquid and particulate contaminants from molten metals  

DOE Patents (OSTI)

Method and apparatus for removal of nonelectrically-conducting gaseous, liquid, and particulate contaminants from molten metal compositions by applying a force thereto. The force (commonly referred to as the Lorentz Force) exerted by simultaneous application of an electric field and a magnetic field on a molten conductor causes an increase, in the same direction as the force, in the apparent specific gravity thereof, but does not affect the nonconducting materials. This difference in apparent densities cause the nonconducting materials to "float" in the opposite direction from the Lorentz Force at a rapid rate. Means are further provided for removal of the contaminants and prevention of stirring due to rotational forces generated by the applied fields.

Hobson, David O. (Oak Ridge, TN); Alexeff, Igor (Oak Ridge, TN); Sikka, Vinod K. (Clinton, TN)

1988-01-01T23:59:59.000Z

112

Method and apparatus for removal of gaseous, liquid and particulate contaminants from molten metals  

DOE Patents (OSTI)

Method and apparatus for removal of nonelectrically-conducting gaseous, liquid, and particulate contaminants from molten metal compositions by applying a force thereto. The force (commonly referred to as the Lorentz Force) exerted by simultaneous application of an electric field and a magnetic field on a molten conductor causes an increase, in the same direction as the force, in the apparent specific gravity thereof, but does not affect the nonconducting materials. This difference in apparent densities cause the nonconducting materials to ''float'' in the opposite direction from the Lorentz Force at a rapid rate. Means are further provided for removal of the contaminants and prevention of stirring due to rotational forces generated by the applied fields. 6 figs.

Hobson, D.O.; Alexeff, I.; Sikka, V.K.

1987-08-10T23:59:59.000Z

113

Removal of NOx or its conversion into harmless gases by charcoals and composites of metal oxides  

SciTech Connect

In recent years, much attention has been devoted to environmental problems such as acid rain, photochemical smog and water pollution. In particular, NOx emissions from factories, auto mobiles, etc. in urban areas have become worse. To solve these problems on environmental pollution on a global scale, the use of activated charcoal to reduce air pollutants is increasing. However, the capability of wood-based charcoal materials is not yet fully known. The removal of NOx or its conversion into harmless gases such as N{sub 2} should be described. In this study, the adsorption of NO over wood charcoal or metal oxide-dispersed wood charcoal was investigated. In particular, carbonized wood powder of Sugi (Cryptomeria japonica D. Don) was used to study the effectivity of using these materials in adsorbing NOx. Since wood charcoal is chemically stable, metal oxide with the ability of photocatalysis was dispersed into wood charcoal to improve its adsorption and capability to use the light energy effectively.

Ishihara, Shigehisa; Furutsuka, Takeshi [Kyoto Univ. (Japan)

1996-12-31T23:59:59.000Z

114

Effect Of Solid Phase Organic Substrate Characteristics On Sulfate Reducer Activity And Metal Removal  

E-Print Network (OSTI)

Abstract. This paper is a progress report on studies whose objectives are to determine methods of analysis that will rate metal sorption and sulfate reduction activity of organic materials for use in passive treatment systems (PTS). Substrates tested include agricultural residues (alfalfa pellets, sugar beat pulp pellets, brewery waste, corncobs, and walnut hulls), inoculums (dairy manure and wetland inoculum), and a variety woods (maple, oak, pine, poplar, and walnut). Characteristics targeted include moisture, organic and nutrient content; water, ethanol and acid soluble and insoluble fractions and metal sorption capacity. The short-term and long-term effects of organic substrate characteristics on metal removal and sulfate reduction rate are being evaluated in batch and column experiments receiving mine water. These data are not presented in this paper but will be included in the oral presentation. Measured values of moisture and organic content ranged from 5.5 to 65 % and 7.4 to 95 % relative to raw sample weights, respectively. The water-soluble fractions and protein content ranged from 0 to 32 % and 2 to 23 % relative to dried samples, respectively. Low concentration zinc sorption studies were described well by Freundlich isotherms. Using a wider range of concentrations, manganese sorption to substrates was more closely modeled by Langmuir isotherms. The highest manganese sorption was observed for manure, corncobs, walnut hulls and wetland inoculum (8-13 mg Mn / gram substrate at an equilibrium concentration (Ce) = 50 mg/L Mn). Corncobs and walnut hulls can be included in substrate specifications to target manganese removal. Moisture and organic content are important parameters in the specification of organic substrates as a significant portion of the raw organic substrate weight can be inorganic. A high soluble fraction should correlate with a rapid startup of SRB activity and thus is an important element in substrate specification. All substrates have some capacity for metal sorption and their quantification is essential for use in PTS.

J. Seyler; L. Figueroa; D. Ahmann; T. R. Wildeman; M. Robustelli

2003-01-01T23:59:59.000Z

115

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

DOE Patents (OSTI)

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

Gorin, Everett (San Rafael, CA)

1981-01-01T23:59:59.000Z

116

NEW HUBBLE SPACE TELESCOPE OBSERVATIONS OF HEAVY ELEMENTS IN FOUR METAL-POOR STARS  

Science Conference Proceedings (OSTI)

Elements heavier than the iron group are found in nearly all halo stars. A substantial number of these elements, key to understanding neutron-capture nucleosynthesis mechanisms, can only be detected in the near-ultraviolet. We report the results of an observing campaign using the Space Telescope Imaging Spectrograph on board the Hubble Space Telescope to study the detailed heavy-element abundance patterns in four metal-poor stars. We derive abundances or upper limits from 27 absorption lines of 15 elements produced by neutron-capture reactions, including seven elements (germanium, cadmium, tellurium, lutetium, osmium, platinum, and gold) that can only be detected in the near-ultraviolet. We also examine 202 heavy-element absorption lines in ground-based optical spectra obtained with the Magellan Inamori Kyocera Echelle Spectrograph on the Magellan-Clay Telescope at Las Campanas Observatory and the High Resolution Echelle Spectrometer on the Keck I Telescope on Mauna Kea. We have detected up to 34 elements heavier than zinc. The bulk of the heavy elements in these four stars are produced by r-process nucleosynthesis. These observations affirm earlier results suggesting that the tellurium found in metal-poor halo stars with moderate amounts of r-process material scales with the rare earth and third r-process peak elements. Cadmium often follows the abundances of the neighboring elements palladium and silver. We identify several sources of systematic uncertainty that must be considered when comparing these abundances with theoretical predictions. We also present new isotope shift and hyperfine structure component patterns for Lu II and Pb I lines of astrophysical interest.

Roederer, Ian U.; Thompson, Ian B. [Carnegie Observatories, Pasadena, CA 91101 (United States); Lawler, James E. [Department of Physics, University of Wisconsin, Madison, WI 53706 (United States); Sobeck, Jennifer S. [Department of Astronomy and Astrophysics, University of Chicago, Chicago, IL 60637 (United States); Beers, Timothy C. [National Optical Astronomy Observatory, Tucson, AZ 85719 (United States); Cowan, John J. [Homer L. Dodge Department of Physics and Astronomy, University of Oklahoma, Norman, OK 73019 (United States); Frebel, Anna [Massachusetts Institute of Technology, Kavli Institute for Astrophysics and Space Research, Cambridge, MA 02139 (United States); Ivans, Inese I. [Department of Physics and Astronomy, University of Utah, Salt Lake City, UT 84112 (United States); Schatz, Hendrik [Department of Physics and Astronomy, Michigan State University, E. Lansing, MI 48824 (United States); Sneden, Christopher [Department of Astronomy, University of Texas at Austin, Austin, TX 78712 (United States)

2012-12-15T23:59:59.000Z

117

Placental concentrations of heavy metals in a mother-child cohort  

SciTech Connect

Heavy metals are environmental contaminants with properties known to be toxic for wildlife and humans. Despite strong concerns about their harmful effects, little information is available on intrauterine exposure in humans. The aim of this study was to evaluate prenatal exposure to As, Cd, Cr, Hg, Mn, and Pb and its association with maternal factors in a population-based mother-child cohort in Southern Spain. Between 2000 and 2002, 700 pregnant women were recruited and 137 placentas from the cohort were randomly selected and analyzed for the selected metals by atomic absorption. Maternal sociodemographic and lifestyle factors were obtained by questionnaire after delivery. Bivariate analysis and multivariate linear regression were performed. Cd and Mn concentrations were detected in all placentas, while Cr, Pb, and Hg were found in 98.5%, 35.0%, and 30.7% of samples, respectively. The highest concentrations were observed for Pb (mean: 94.80 ng/g wet weight of placenta), followed by Mn (63.80 ng/g), Cr (63.70 ng/g), Cd (3.45 ng/g), and Hg (0.024 ng/g). Arsenic was not detected in any sample. Gestational age and smoking during pregnancy were associated with placental Cd concentrations, while no factor appeared to influence concentrations of Cr, Hg, Mn, or Pb. In comparison to results of European studies, these concentrations are in a low-intermediate position. Studies are required to investigate the factors contributing to early exposure to heavy metals and to determine how placental transfer of these toxic compounds may affect children's health.

Amaya, E., E-mail: eamayag@ugr.es [Laboratory of Medical Investigations, San Cecilio University Hospital, University of Granada, 18071 Granada (Spain); Gil, F. [Department of Legal Medicine, Toxicology and Physic Anthropology, Faculty of Medicine, University of Granada, 18071 Granada (Spain)] [Department of Legal Medicine, Toxicology and Physic Anthropology, Faculty of Medicine, University of Granada, 18071 Granada (Spain); Freire, C. [Laboratory of Medical Investigations, San Cecilio University Hospital, University of Granada, 18071 Granada (Spain) [Laboratory of Medical Investigations, San Cecilio University Hospital, University of Granada, 18071 Granada (Spain); National School of Public Health, Oswaldo Cruz Foundation (FIOCRUZ), 21041-210 Rio de Janeiro (Brazil); Olmedo, P. [Department of Legal Medicine, Toxicology and Physic Anthropology, Faculty of Medicine, University of Granada, 18071 Granada (Spain)] [Department of Legal Medicine, Toxicology and Physic Anthropology, Faculty of Medicine, University of Granada, 18071 Granada (Spain); Fernandez-Rodriguez, M. [Laboratory of Medical Investigations, San Cecilio University Hospital, University of Granada, 18071 Granada (Spain)] [Laboratory of Medical Investigations, San Cecilio University Hospital, University of Granada, 18071 Granada (Spain); Fernandez, M.F.; Olea, N. [Laboratory of Medical Investigations, San Cecilio University Hospital, University of Granada, 18071 Granada (Spain) [Laboratory of Medical Investigations, San Cecilio University Hospital, University of Granada, 18071 Granada (Spain); CIBER de Epidemiologia y Salud Publica (CIBERESP) (Spain)

2013-01-15T23:59:59.000Z

118

EM Task 13 -- Cone penetrometer for subsurface heavy metals detection. Semi-annual report, April 1--September 30, 1997  

SciTech Connect

Surface and subsurface contamination of soils by heavy metals, including Pb, Cr, Cu, Zn, and Cd has become an area of concern for many industrial and government organizations. Conventional sampling and analysis techniques for soil provide a high degree of sensitivity and selectivity for individual analytes. However, obtaining a representative sampling and analysis from a particular site using conventional techniques is time-consuming and costly. Additionally, conventional methods are difficult to implement in the field for in situ and/or real-time applications. Therefore, there is a need for characterization and monitoring techniques for heavy metals in soils which allow cost-effective, rapid, in situ measurements. Laser induced breakdown spectroscopy (LIBS) has been used to successfully measure metals content in a variety of matrices including soil. Science and Engineering Associates (SEA) is developing a subsurface cone penetrometer (CPT) probe for heavy metal detection that employs LIBS. The LIBS/CPT unit is to be applied to in situ, real-time sampling and analysis of heavy metals in soil. The overall objectives of this project are to evaluate potential calibration techniques for the LIBS/CPT instrument and to provide a preliminary evaluation of the LIBS instrument calibration using samples obtained from the field.

Grisanti, A.A.; Timpe, R.C.; Foster, H.J.; Eylands, K.E.; Crocker, C.R.

1997-12-31T23:59:59.000Z

119

The Removal of Heavy Metals and Upgrading Crude Bio-oil from ...  

Science Conference Proceedings (OSTI)

As a potential method to detoxify the biomass and to convert this material to a suitable bio-energy resource, the hydrothermal upgrading process was applied to ...

120

Removal of Heavy Metals from Water by Fly Ash from Coal and Steel ...  

Science Conference Proceedings (OSTI)

In this work, iron dust from steelmaking process and coal fly ahs are used as an alternative adsorbent ... iNEMI Environmental Thrust; History, Challenges, & Opportunities ... Phosphorus Flow Analysis for Food Production and Consumption.

Note: This page contains sample records for the topic "heavy metals removal" 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.


121

Applications of porous electrodes to metal-ion removal and the design of battery systems  

DOE Green Energy (OSTI)

This dissertation treats the use of porous electrodes as electrochemical reactors for the removal of dilute metal ions. A methodology for the scale-up of porous electrodes used in battery applications is given. Removal of 4 ..mu..g Pb/cc in 1 M sulfuric acid was investigated in atmospheric and high-pressure, flow-through porous reactors. The atmospheric reactor used a reticulated vitreous carbon porous bed coated in situ with a mercury film. Best results show 98% removal of lead from the feed stream. Results are summarized in a dimensionless plot of Sherwood number vs Peclet number. High-pressure, porous-electrode experiments were performed to investigate the effect of pressure on the current efficiency. Pressures were varied up to 120 bar on electrode beds of copper or lead-coated spheres. The copper spheres showed high hydrogen evolution rates which inhibited lead deposition, even at high cathodic overpotentials. Use of lead spheres inhibited hydrogen evolution but often resulted in the formation of lead sulfate layers; these layers were difficult to reduce back to lead. Experimental data of one-dimensional porous battery electrodes are combined with a model for the current collector and cell connectors to predict ultimate specific energy and maximum specific power for complete battery systems. Discharge behavior of the plate as a whole is first presented as a function of depth of discharge. These results are combined with the voltage and weight penalties of the interconnecting bus and post, positive and negative active material, cell container, etc. to give specific results for the lithium-aluminum/iron sulfide high-temperature battery. Subject to variation is the number of positive electrodes, grid conductivity, minimum current-collector weight, and total delivered capacity. The battery can be optimized for maximum energy or power, or a compromise design may be selected.

Trost, G.G.

1983-09-01T23:59:59.000Z

122

Use of MgO doped with a divalent or trivalent metal cation for removing arsenic from water  

DOE Patents (OSTI)

Systems and methods for use of magnesium hydroxide, either directly or through one or more precursors, doped with a divalent or trivalent metal cation, for removing arsenic from drinking water, including water distribution systems. In one embodiment, magnesium hydroxide, Mg(OH).sub.2 (a strong adsorbent for arsenic) doped with a divalent or trivalent metal cation is used to adsorb arsenic. The complex consisting of arsenic adsorbed on Mg(OH).sub.2 doped with a divalent or trivalent metal cation is subsequently removed from the water by conventional means, including filtration, settling, skimming, vortexing, centrifugation, magnetic separation, or other well-known separation systems. In another embodiment, magnesium oxide, MgO, is employed, which reacts with water to form Mg(OH).sub.2. The resulting Mg(OH).sub.2 doped with a divalent or trivalent metal cation, then adsorbs arsenic, as set forth above. The method can also be used to treat human or animal poisoning with arsenic.

Moore, Robert C; Holt-Larese, Kathleen C; Bontchev, Ranko

2013-08-13T23:59:59.000Z

123

Heavy Element Dispersion in the Metal-Poor Globular Cluster M92  

E-Print Network (OSTI)

Dispersion among the light elements is common in globular clusters (GCs), while dispersion among heavier elements is less common. We present detection of r-process dispersion relative to Fe in 19 red giants of the metal-poor GC M92. Using spectra obtained with the Hydra multi-object spectrograph on the WIYN Telescope at Kitt Peak National Observatory, we derive differential abundances for 21 species of 19 elements. The Fe-group elements, plus Y and Zr, are homogeneous at a level of 0.07-0.16 dex. The heavy elements La, Eu, and Ho exhibit clear star-to-star dispersion spanning 0.5-0.8 dex. The abundances of these elements are correlated with one another, and we demonstrate that they were produced by r-process nucleosynthesis. This r-process dispersion is not correlated with the dispersion in C, N, or Na in M92, indicating that r-process inhomogeneities were present in the gas throughout star formation. The r-process dispersion is similar to that previously observed in the metal-poor GC M15, but its origin in M...

Roederer, Ian U

2011-01-01T23:59:59.000Z

124

HEAVY-ELEMENT DISPERSION IN THE METAL-POOR GLOBULAR CLUSTER M92  

SciTech Connect

Dispersion among the light elements is common in globular clusters (GCs), while dispersion among heavier elements is less common. We present detection of r-process dispersion relative to Fe in 19 red giants of the metal-poor GC M92. Using spectra obtained with the Hydra multi-object spectrograph on the WIYN Telescope at Kitt Peak National Observatory, we derive differential abundances for 21 species of 19 elements. The Fe-group elements, plus Y and Zr, are homogeneous at a level of 0.07-0.16 dex. The heavy-elements La, Eu, and Ho exhibit clear star-to-star dispersion spanning 0.5-0.8 dex. The abundances of these elements are correlated with one another, and we demonstrate that they were produced by r-process nucleosynthesis. This r-process dispersion is not correlated with the dispersion in C, N, or Na in M92, indicating that r-process inhomogeneities were present in the gas throughout star formation. The r-process dispersion is similar to that previously observed in the metal-poor GC M15, but its origin in M15 or M92 is unknown at present.

Roederer, Ian U. [Carnegie Observatories, 813 Santa Barbara Street, Pasadena, CA 91101 (United States); Sneden, Christopher, E-mail: iur@obs.carnegiescience.edu [Department of Astronomy, University of Texas at Austin, 1 University Station, C1400, Austin, TX 78712 (United States)

2011-07-15T23:59:59.000Z

125

Ion Removal  

INL’s ion removal technology leverages the ability of phosphazene polymers discriminate between water and metal ions, which allows water to pass ...

126

Process for removing and detoxifying cadmium from scrap metal including mixed waste  

SciTech Connect

Cadmium-bearing scrap from nuclear applications, such as neutron shielding and reactor control and safety rods, must usually be handled as mixed waste since it is radioactive and the cadmium in it is both leachable and highly toxic. Removing the cadmium from this scrap, and converting it to a nonleachable and minimally radioactive form, would greatly simplify disposal or recycling. A process now under development will do this by shredding the scrap; leaching it with reagents which selectively dissolve out the cadmium; reprecipitating the cadmium as its highly insoluble sulfide; then fusing the sulfide into a glassy matrix to bring its leachability below EPA limits before disposal. Alternatively, the cadmium may be recovered for reuse. A particular advantage of the process is that all reagents (except the glass frit) can easily be recovered and reused in a nearly closed cycle, minimizing the risk of radioactive release. The process does not harm common metals such as aluminum, iron and stainless steel, and is also applicable to non-nuclear cadmium-bearing scrap such as nickel-cadmium batteries.

Kronberg, J.W.

1994-07-01T23:59:59.000Z

127

Purification of alkali metal nitrates  

DOE Patents (OSTI)

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

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

1985-05-14T23:59:59.000Z

128

Heavy metals and toxic organic pollutants in MSW-composts: Research results on phytoavailability, bioavailability, fate, etc  

Science Conference Proceedings (OSTI)

The paper is a review and interpretation of research which has been conducted to determine the fate, transport, and potential effects of heavy metals and toxic organic compounds in Municipal Solid Waste (MSW)-composts and sewage sludges. Evaluation of research findings identified a number of pathways by which these contaminants can be transferred from MSW-compost or compost-amended soils to humans, livestock, or wildlife. The pathways consider direct ingestion of compost or compost-amended soil by livestock and children, plant uptake by food or feed crops, and exposure to dust, vapor, and water to which metals and organics have migrated.

Ryan, J.A.; Chaney, R.L.

1994-01-01T23:59:59.000Z

129

Reducing volatilization of heavy metals in phosphate-pretreated municipal solid waste incineration fly ash by forming pyromorphite-like minerals  

Science Conference Proceedings (OSTI)

This research investigated the feasibility of reducing volatilization of heavy metals (lead, zinc and cadmium) in municipal solid waste incineration (MSWI) fly ash by forming pyromorphite-like minerals via phosphate pre-treatment. To evaluate the evaporation characteristics of three heavy metals from phosphate-pretreated MSWI fly ash, volatilization tests have been performed by means of a dedicated apparatus in the 100-1000 deg. C range. The toxicity characteristic leaching procedure (TCLP) test and BCR sequential extraction procedure were applied to assess phosphate stabilization process. The results showed that the volatilization behavior in phosphate-pretreated MSWI fly ash could be reduced effectively. Pyromorphite-like minerals formed in phosphate-pretreated MSWI fly ash were mainly responsible for the volatilization reduction of heavy metals in MSWI fly ash at higher temperature, due to their chemical fixation and thermal stabilization for heavy metals. The stabilization effects were encouraging for the potential reuse of MSWI fly ash.

Sun Ying; Zheng Jianchang [School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China); Zou Luquan [Shanghai Center of Solid Waste Disposal, Shanghai (China); Liu Qiang; Zhu Ping [School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China); Qian Guangren, E-mail: grqian@mail.shu.edu.cn [School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China)

2011-02-15T23:59:59.000Z

130

Metal-fueled HWR (heavy water reactors) severe accident issues: Differences and similarities to commercial LWRs (light water reactors)  

DOE Green Energy (OSTI)

Differences and similarities in severe accident progression and phenomena between commercial Light Water Reactors (LWR) and metal-fueled isotopic production Heavy Water Reactors (HWR) are described. It is very important to distinguish between accident progression in the two systems because each reactor type behaves in a unique manner to a fuel melting accident. Some of the lessons learned as a result of the extensive commercial severe accident research are not applicable to metal-fueled heavy water reactors. A direct application of severe accident phenomena developed from oxide-fueled LWRs to metal-fueled HWRs may lead to large errors or substantial uncertainties. In general, the application of severe accident LWR concepts to HWRs should be done with the intent to define the relevant issues, define differences, and determine areas of overlap. This paper describes the relevant differences between LWR and metal-fueled HWR severe accident phenomena. Also included in the paper is a description of the phenomena that govern the source term in HWRs, the areas where research is needed to resolve major uncertainties, and areas in which LWR technology can be directly applied with few modifications.

Ellison, P.G.; Hyder, M.L.; Monson, P.R. (Westinghouse Savannah River Co., Aiken, SC (USA)); Coryell, E.W. (EG and G Idaho, Inc., Idaho Falls, ID (USA))

1990-01-01T23:59:59.000Z

131

Removal of metal oxide defects through improved semi-anisotropic wet etching process  

E-Print Network (OSTI)

Data recently collected from an industrial thin film manufacturer indicate that almost 8% of devices are rejected due to excess metal, or unwanted metal on the device surface. Experimentation and analysis suggest that ...

Dave, Neha H. (Neha Hemang)

2012-01-01T23:59:59.000Z

132

Carbon Dioxide Removal from Flue Gas Using Microporous Metal Organic Frameworks  

SciTech Connect

UOP LLC, a Honeywell Company, in collaboration with Professor Douglas LeVan at Vanderbilt University (VU), Professor Adam Matzger at the University of Michigan (UM), Professor Randall Snurr at Northwestern University (NU), and Professor Stefano Brandani at the University of Edinburgh (UE), supported by Honeywell's Specialty Materials business unit and the Electric Power Research Institute (EPRI), have completed a three-year project to develop novel microporous metal organic frameworks (MOFs) and an associated vacuum-pressure swing adsorption (vPSA) process for the removal of CO{sub 2} from coal-fired power plant flue gas. The project leveraged the team's complementary capabilities: UOP's experience in materials development and manufacturing, adsorption process design and process commercialization; LeVan and Brandani's expertise in high-quality adsorption measurements; Matzger's experience in syntheis of MOFs and the organic components associated with MOFs; Snurr's expertise in molecular and other modeling; Honeywell's expertise in the manufacture of organic chemicals; and, EPRI's knowledge of power-generation technology and markets. The project was successful in that a selective CO{sub 2} adsorbent with good thermal stability and reasonable contaminant tolerance was discovered, and a low cost process for flue gas CO{sub 2} capture process ready to be evaluated further at the pilot scale was proposed. The team made significant progress toward the current DOE post-combustion research targets, as defined in a recent FOA issued by NETL: 90% CO{sub 2} removal with no more than a 35% increase in COE. The team discovered that favorable CO{sub 2} adsorption at more realistic flue gas conditions is dominated by one particular MOF structure type, M/DOBDC, where M designates Zn, Co, Ni, or Mg and DOBDC refers to the form of the organic linker in the resultant MOF structure, dioxybenzenedicarboxylate. The structure of the M/DOBDC MOFs consists of infinite-rod secondary building units bound by DOBDC resulting in 1D hexagonal pores about 11 angstroms in diameter. Surface areas range from 800 to 1500 sq m/g for the different MOFs. Mg/DOBDC outperformed all MOF and zeolite materials evaluated to date, with about 25 wt% CO{sub 2} captured by this MOF at flue gas conditions ({approx}0.13 atm CO{sub 2} pressure, 311K). In simulated flue gas without oxygen, the zero-length (ZLC) system was very useful in quickly simulating the effect of long term exposure to impurities on the MOFs. Detailed adsorption studies on MOF pellets have shown that water does not inhibit CO{sub 2} adsorption for MOFs as much as it does for typical zeolites. Moreover, some MOFs retain a substantial CO{sub 2} capacity even with a modest water loading at room temperature. Molecular modeling was a key activity in three areas of our earlier DOE/NETL-sponsored MOF-based research on CC. First, the team was able to effectively simulate CO{sub 2} and other gas adsorption isotherms for more than 20 MOFs, and the knowledge obtained was used to help predict new MOF structures that should be effective for CO{sub 2} adsorption at low pressure. The team also showed that molecular modeling could be utilized to predict the hydrothermal stability of a given MOF. Finally, the team showed that low moisture level exposure actually enhanced the CO{sub 2} adsorption performance of a particular MOF, HKUST-1.

David A Lesch

2010-06-30T23:59:59.000Z

133

Thermodynamic analysis on heavy metals partitioning impacted by moisture during the MSW incineration  

Science Conference Proceedings (OSTI)

Highlights: Black-Right-Pointing-Pointer Partitioning of HMs affected by moisture was investigated by thermodynamic analysis. Black-Right-Pointing-Pointer Increase in moisture and in temperature was opposite impact on HMs contribution. Black-Right-Pointing-Pointer The extent of temperature decreased by increase in moisture determines the impact. - Abstract: A thermodynamic calculation was carried out to predict the behavior and speciation of heavy metals (HMs), Pb, Zn, Cu, and Cd, during municipal solid waste (MSW) incineration with the different moisture levels. The calculation was based on the minimization of the total Gibbs free energy of the multi-components and multi-phases closed system reaching chemical equilibrium. The calculation also indicated the reaction directions and tendencies of HMs components. The impacts of chlorine additives (No PVC, 1%PVC, and 5%PVC) and moisture on the behavior of HMs were investigated at different temperature levels in the system (750 Degree-Sign C, 950 Degree-Sign C, and 1150 Degree-Sign C). Furthermore, because the incineration temperature falls down with the increase in moisture in waste, the co-influence of moisture and temperature in combusting MSW on the HMs was also studied with the given chlorine (as 1%PVC + 0.5%NaCl). The results showed that in the non-chlorine system, the impact of the moisture on Pb, Zn, and Cu was not significant, and the ratio of compound transformation was less than 10%, except the Cd compounds at 950 Degree-Sign C and 1150 Degree-Sign C. In the system with low chlorine (as 1%PVC) at constant temperature, the chlorides of HMs (Cd, Pb, Zn, and Cu) transferred to oxides, and when the content of chlorine rose up (as 5%PVC), the ratio of the chlorides of HMs (Cd, Pb, Zn, and Cu) transferring to oxides fell down noticeably. When the moisture varied together with the temperature, the Zn and Cu compounds transferred from chlorides to oxides with increase in moisture as well as decrease in temperature. At the temperature of 700-1000 Degree-Sign C, the impact of temperature on Pb and Cd was little and the moisture was the main factor; while at the temperature of 1000-1200 Degree-Sign C, the impact of increase in moisture and decrease in temperature on Pb and Cd was almost equal and reversed.

Zhang Yanguo; Li Qinghai; Jia Jinyan [Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Meng Aihong, E-mail: mengah@tsinghua.edu.cn [Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Department of Environmental Science and Technology, Tsinghua University, Beijing 100084 (China)

2012-12-15T23:59:59.000Z

134

Heavy metal inventory and fuel sustainability of recycling TRU in FBR design  

Science Conference Proceedings (OSTI)

Nuclear fuel materials from spent fuel of light water reactors have a potential to be used for destructive devices with very huge energy release or in the same time, it can be utilized as a peaceful energy or civil applications, for generating electricity, desalination of water, medical application and others applications. Several research activities showed some recycled spent fuel can be used as additional fuel loading for increasing fuel breeding capability as well as improving intrinsic aspect of nuclear non-proliferation. The present investigation intends to evaluate the composition of heavy metals inventories and fuel breeding capability in the FBR design based on the loaded fuel of light water reactor (LWR) spent fuel (SF) of 33 GWd/t with 5 years cooling time by adopting depletion code of ORIGEN. Whole core analysis of FBR design is performed by adopting and coupling codes such as SLAROM code, JOINT and CITATION codes. Nuclear data library, JFS-3-J-3.2R which is based on the JENDL 3.2 has been used for nuclear data analysis. JSFR design is the basis design reference which basically adopted 800 days cycle length for 4 batches system. Higher inventories of plutonium of MOX fuel and TRU fuel types at equilibrium composition than initial composition have been shown. Minor actinide (MA) inventory compositions obtain a different inventory trends at equilibrium composition for both fuel types. Higher Inventory of MA is obtained by MOX fuel and less MA inventory for TRU fuel at equilibrium composition than initial composition. Some different MA inventories can be estimated from the different inventory trend of americium (Am). Higher americium inventory for MOX fuel and less americium inventory for TRU fuel at equilibrium condition. Breeding ratio of TRU fuel is relatively higher compared with MOX fuel type. It can be estimated from relatively higher production of Pu-238 (through converted MA) in TRU fuel, and Pu-238 converts through neutron capture to produce Pu-239. Higher breeding ratio of MOX fuel and TRU fuel types at equilibrium condition are estimated from converted fertile material during reactor operation into fissile material of plutonium such as converted uranium fuel (converted U-238 into Pu-239) or additional converted fuel from MA into Pu-238 and changes into Pu-239 by capturing neutron. Loading LWR SF gives better fuel breeding capability and increase inventory of MA for doping material of MOX fuel; however, it requires more supply MA inventory for TRU fuel type.

Permana, Sidik; Suzuki, Mitsutoshi; Su'ud, Zaki [Department of Science and Technology for Nuclear Material Management (STNM), Japan Atomic Energy Agency (JAEA), 2-4 Shirane, Shirakata, Tokai Mura, Naka-gun, Ibaraki 319-1195 Nuclear Physics and Bio (Indonesia); Department of Science and Technology for Nuclear Material Management (STNM), Japan Atomic Energy Agency (JAEA), 2-4 Shirane, Shirakata, Tokai Mura, Naka-gun, Ibaraki 319-1195 (Japan); Nuclear Physics and Bio Physics Research Group, Department of Physics, Bandung Institute of Technology, Gedung Fisika, Jl. Ganesha 10, Bandung 40132 (Indonesia)

2012-06-06T23:59:59.000Z

135

Multipollutant Removal with WOWClean® System  

E-Print Network (OSTI)

WOW Energy built and tested its multipollutant removal WOWClean® system in a development program with the Texas Commission on Environmental Quality (TCEQ). A 2,500 ACFM mobile unit was built to field test the removal of air pollution constituents from the flue gas of a power plant and demonstrate the technology. The system integrates proven emission reduction techniques into a single, multi-pollutant reduction system and is designed to remove Mercury, SOx, NOx, particulates, heavy metals and other pollutants from low temperature flue gases. Its advantages include robust operation, lower investment, lower operating cost and high removal rates. The WOWClean® system has been tested on flue gases resulting from the combustion of diverse fuels such as petcoke, coal, wood, diesel and natural gas. In addition to significant removal of CO2, test results demonstrate the capability to reduce 99.5% SOx (from levels as high as 2200 ppm), 90% reduction of NOx, and > 90% heavy metals. The paper will include details of the multi-pollutant system along with test results.

Romero, M.

2010-01-01T23:59:59.000Z

136

In situ removal of contamination from soil  

DOE Patents (OSTI)

A process of remediation of cationic heavy metal contamination from soil utilizes gas phase manipulation to inhibit biodegradation of a chelating agent that is used in an electrokinesis process to remove the contamination, and further gas phase manipulation to stimulate biodegradation of the chelating agent after the contamination has been removed. The process ensures that the chelating agent is not attacked by bioorganisms in the soil prior to removal of the contamination, and that the chelating agent does not remain as a new contaminant after the process is completed.

Lindgren, Eric R. (Albuquerque, NM); Brady, Patrick V. (Albuquerque, NM)

1997-01-01T23:59:59.000Z

137

FIELD DEMONSTRATION OF A MEMBRANE PROCESS TO RECOVER HEAVY HYDROCARBONS AND TO REMOVE WATER FROM NATURAL GAS  

SciTech Connect

The objective of this project is to design, construct and field demonstrate a membrane system to recover natural gas liquids (NGL) and remove water from raw natural gas. An extended field test to demonstrate system performance under real-world conditions would convince industry users of the efficiency and reliability of the process. The system has been designed and fabricated by Membrane Technology and Research, Inc. (MTR) and will be installed and operated at British Petroleum (BP)-Amoco's Pascagoula, MS plant. The Gas Research Institute will partially support the field demonstration and BP-Amoco will help install the unit and provide onsite operators and utilities. The gas processed by the membrane system will meet pipeline specifications for dewpoint and Btu value and can be delivered without further treatment to the pipeline. Based on data from prior membrane module tests, the process is likely to be significantly less expensive than glycol dehydration followed by propane refrigeration, the principal competitive technology. At the end of this demonstration project the process will be ready for commercialization. The route to commercialization will be developed during this project and may involve collaboration with other companies already servicing the natural gas processing industry.

R. Baker; R. Hofmann; K.A. Lokhandwala

2003-02-14T23:59:59.000Z

138

Field Demonstration of a Membrane Process to Recover Heavy Hydrocarbons and to Remove Water from Natural Gas  

SciTech Connect

The objective of this project is to design, construct and field demonstrate a membrane system to recover natural gas liquids (NGL) and remove water from raw natural gas. An extended field test to demonstrate system performance under real-world conditions would convince industry users of the efficiency and reliability of the process. The system has been designed and fabricated by Membrane Technology and Research, Inc. (MTR) and will be installed and operated at British Petroleum (BP)-Amoco's Pascagoula, MS plant. The Gas Research Institute will partially support the field demonstration and BP-Amoco will help install the unit and provide onsite operators and utilities. The gas processed by the membrane system will meet pipeline specifications for dewpoint and BTU value and can be delivered without further treatment to the pipeline. Based on data from prior membrane module tests, the process is likely to be significantly less expensive than glycol dehydration followed by propane refrigeration, the principal competitive technology. At the end of this demonstration project the process will be ready for commercialization. The route to commercialization will be developed during this project and may involve collaboration with other companies already servicing the natural gas processing industry.

R. Baker; T. Hofmann; K. A. Lokhandwala

2004-09-29T23:59:59.000Z

139

Field Demonstration of a Membrane Process to Recover Heavy Hydrocarbons and to Remove Water from Natural Gas  

SciTech Connect

The objective of this project is to design, construct and field demonstrate a membrane system to recover natural gas liquids (NGL) and remove water from raw natural gas. An extended field test to demonstrate system performance under real-world high-pressure conditions is being conducted to convince industry users of the efficiency and reliability of the process. The system was designed and fabricated by Membrane Technology and Research, Inc. (MTR) and installed and operated at BP Amoco's Pascagoula, MS plant. The Gas Research Institute is partially supporting the field demonstration and BP-Amoco helped install the unit and provided onsite operators and utilities. The gas processed by the membrane system meets pipeline specifications for dewpoint and BTU value and can be delivered without further treatment to the pipeline. Based on data from prior membrane module tests, the process is likely to be significantly less expensive than glycol dehydration followed by propane refrigeration, the principal competitive technology. During the course of this project, MTR has sold 11 commercial units related to the field test technology, and by the end of this demonstration project the process will be ready for broader commercialization. A route to commercialization has been developed during this project and involves collaboration with other companies already servicing the natural gas processing industry.

R. Baker; T. Hofmann; K. A. Lokhandwala

2005-09-29T23:59:59.000Z

140

Field Demonstration of a Membrane Process to Recover Heavy Hydrocarbons and to Remove Water from Natural Gas  

SciTech Connect

The objective of this project was to design, construct and field demonstrate a membrane system to recover natural gas liquids (NGL) and remove water from raw natural gas. An extended field test to demonstrate system performance under real-world high-pressure conditions was conducted to convince industry users of the efficiency and reliability of the process. The system was designed and fabricated by Membrane Technology and Research, Inc. (MTR) and installed and operated at BP Amoco's Pascagoula, MS plant. The Gas Research Institute partially supported the field demonstration and BP-Amoco helped install the unit and provide onsite operators and utilities. The gas processed by the membrane system meets pipeline specifications for dew point and BTU value and can be delivered without further treatment to the pipeline. During the course of this project, MTR has sold thirteen commercial units related to the field test technology. Revenue generated from new business is already more than four times the research dollars invested in this process by DOE. The process is ready for broader commercialization and the expectation is to pursue the commercialization plans developed during this project, including collaboration with other companies already servicing the natural gas processing industry.

Kaaeid Lokhandwala

2007-03-30T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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
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141

Field Demonstration of a Membrane Process to Recover Heavy Hydrocarbons and to Remove Water from Natural Gas  

Science Conference Proceedings (OSTI)

The objective of this project is to design, construct and field demonstrate a membrane system to recover natural gas liquids (NGL) and remove water from raw natural gas. An extended field test to demonstrate system performance under real-world high-pressure conditions is being conducted to convince industry users of the efficiency and reliability of the process. The system was designed and fabricated by Membrane Technology and Research, Inc. (MTR) and installed and operated at BP Amoco's Pascagoula, MS plant. The Gas Research Institute is partially supporting the field demonstration and BP-Amoco helped install the unit and provides onsite operators and utilities. The gas processed by the membrane system meets pipeline specifications for dew point and BTU value and can be delivered without further treatment to the pipeline. Based on data from prior membrane module tests, the process is likely to be significantly less expensive than glycol dehydration followed by propane refrigeration, the principal competitive technology. During the course of this project, MTR has sold 13 commercial units related to the field test technology, and by the end of this demonstration project the process will be ready for broader commercialization. A route to commercialization has been developed during this project and involves collaboration with other companies already servicing the natural gas processing industry.

R. Baker; T. Hofmann; K. A. Lokhandwala

2006-09-29T23:59:59.000Z

142

Methods for producing hydrogen (BI) sulfide and/or removing metals  

DOE Patents (OSTI)

The present invention is a process wherein sulfide production by bacteria is efficiently turned on and off, using pH adjustment. The adjustment of pH impacts sulfide production by bacteria by altering the relative amounts of H.sub.2 S and HS-- in solution and thereby control the inhibition of the bacterial metabolism that produces sulfide. This process can be used to make a bioreactor produce sulfide "on-demand" so that the production of sulfide can be matched to its use as a metal precipitation reagent. The present invention is of significance because it enables the use of a biological reactor, a cost effective sulfide production system, by making the biological reactor produce hydrogen sulfide "on demand", and therefore responsive to production schedules, waste stream generation rate, and health and safety requirements/goals.

Truex, Michael J [Richland, WA; Peyton, Brent M [Pullman, WA; Toth, James J [Kennewick, WA

2002-05-14T23:59:59.000Z

143

Method for mobilization of hazardous metal ions in soils  

DOE Patents (OSTI)

A microbial process for removing heavy metals such as bismuth, cadmium, lead, thorium, uranium and other transuranics from soils and sediments, utilizing indigenous, or isolates of indigenous, microorganisms and reducing agents, such as cysteine or sodium thioglycollate, or complexing agents such as the amino acid glycine, to effect the mobilization or release of the metals from the soil particles.

Dugan, Patrick R. (Idaho Falls, ID); Pfister, Robert M. (Powell, OH)

1995-01-01T23:59:59.000Z

144

An ecological study examining the correlation of end-stage renal disease and ground water heavy metal content in Texas counties  

E-Print Network (OSTI)

An ecological study was conducted to examine the correlation of end-stage renal disease (ESRD) and the ground water heavy metal level of lead, arsenic, cadmium, mercury and the cumulative level of all four metals in Texas counties. The heavy meal dab was collected from the United States Geologic Survey (USGS) measurement and covered the twenty-one year span 1970- 1990. The ESRD data was gathered from the Texas Department of Health Kidney Program ESRD Registry for the five-year span 1988-1992. This registry included more than 99% of incident ESRD cases over the same time period. The 1990 U.S. Census data was used to estimate county population by age, race and sex. Exposure was defined as residence in a county with ground water measurements that fell in the highest quartile for each metal (mercury 0.297ug/, arsenic 3.216ug/l, lead 4.685ug/l, cadmium 1.423ug/l, cumulative metal level 8.911ug/l). Outcome was defined as an incident case of ESRD between the years 1988-1992 and examined as five-year incidence of ESRD per 10,000 persons. Among 254 Texas counties, 52 had at least 7 years of metal measurements for lead and cadmium, 51 counties had at least 7 years of metal measurements for arsenic and mercury and 50 counties had 7 years of measurements for all four metals. Linear and logistic regression procedures were carried out to examine the relationship between heavy metal ground water levels and incidence of ESRD. None of the metals demonstrated a statistically significant positive relationship with five-year incidence of ESRD per 10,000 persons. Counties with high levels of heavy metals did not indicate an increased odds of having a five-year ESRD incidence per 10,000 persons above the 1988-1992 state average. The percentage of Black or Hispanic persons in a county was a positive predictor of increased five-year incidence of ESRD per 10,000 persons.

Bishop, Scott Alan

1999-01-01T23:59:59.000Z

145

Single-layer transition metal sulfide catalysts  

SciTech Connect

Transition Metal Sulfides (TMS), such as molybdenum disulfide (MoS.sub.2), are the petroleum industry's "workhorse" catalysts for upgrading heavy petroleum feedstocks and removing sulfur, nitrogen and other pollutants from fuels. We have developed an improved synthesis technique to produce SLTMS catalysts, such as molybdenum disulfide, with potentially greater activity and specificity than those currently available. Applications for this technology include heavy feed upgrading, in-situ catalysis, bio-fuel conversion and coal liquefaction.

Thoma, Steven G. (Albuquerque, NM)

2011-05-31T23:59:59.000Z

146

Single-layer transition metal sulfide catalysts  

DOE Patents (OSTI)

Transition Metal Sulfides (TMS), such as molybdenum disulfide (MoS.sub.2), are the petroleum industry's "workhorse" catalysts for upgrading heavy petroleum feedstocks and removing sulfur, nitrogen and other pollutants from fuels. We have developed an improved synthesis technique to produce SLTMS catalysts, such as molybdenum disulfide, with potentially greater activity and specificity than those currently available. Applications for this technology include heavy feed upgrading, in-situ catalysis, bio-fuel conversion and coal liquefaction.

Thoma, Steven G. (Albuquerque, NM)

2011-05-31T23:59:59.000Z

147

Use of Sequential Injection Analysis to construct a Potentiometric Electronic Tongue: Application to the Multidetermination of Heavy Metals  

SciTech Connect

An automated potentiometric electronic tongue (ET) was developed for the quantitative determination of heavy metal mixtures. The Sequential Injection Analysis (SIA) technique was used in order to automate the obtaining of input data, and the combined response was modeled by means of Artificial Neural Networks (ANN). The sensor array was formed by four sensors: two based on chalcogenide glasses Cd sensor and Cu sensor, and the rest on poly(vinyl chloride) membranes Pb sensor and Zn sensor. The Ion Selective Electrode (ISE) sensors were first characterized with respect to one and two analytes, by means of high-dimensionality calibrations, thanks to the use of the automated flow system; this characterization enabled an interference study of great practical utility. To take profit of the dynamic nature of the sensor's response, the kinetic profile of each sensor was compacted by Fast Fourier Transform (FFT) and the extracted coefficients were used as inputs for the ANN in the multidetermination applications. In order to identify the ANN which provided the best model of the electrode responses, some of the network parameters were optimized. Finally analyses were performed employing synthetic samples and water samples of the river Ebro; obtained results were compared with reference methods.

Mimendia, Aitor; Merkoci, Arben; Valle, Manel del [Sensors and Biosensors Group, Chemistry Dept., Universitat Autonoma de Barcelona, Edifici Cn, 08193 Bellaterra, Barcelona (Spain); Legin, Andrey [Chemistry Dept, St. Petersburg University, Universitetskaya nab. 7/9, 199034 St. Petersburg (Russian Federation)

2009-05-23T23:59:59.000Z

148

Influence of biologically-active substances on {sup 137}Cs and heavy metals uptake by Barley plant  

SciTech Connect

Available in abstract form only. Full text of publication follows: When solving the problem of contaminated agricultural lands rehabilitation, most of attention is concentrated on the effective means which allow the obtaining of ecologically safe production. The minimization of radionuclides and heavy metals (HM) content in farm products on the basis of their migration characteristics in agro-landscapes and with the regard for different factors influencing contaminants behavior in the soil-plant system is of great significance. Our investigation has shown that the effect of biologically active substances (BAS) using for seeds treatment on {sup 137}Cs transfer to barley grown on Cd contaminated soil was dependent on their properties and dosage, characteristics of soil contamination and biological peculiarities of plants, including stage of plants development. Seeds treatment by plant growth regulator Zircon resulted in a significant increase in {sup 137}Cs activity in harvest (40- 50%), increase in K concentration and significant reduction in Ca concentration. Increased Cd content in soil reduced {sup 137}Cs transfer to barley plants by 30-60% (p<0,05) and Zircon application further reduced its concentration. Ambiol and El also reduced {sup 137}Cs uptake by roots and Cd and Pb phyto-toxicity. The experimental data do not make it possible to link the BAS effect on inhibition of {sup 137}Cs absorption by plants directly with their influence on HM phyto-toxicity. The dependence of Concentration Ratio of {sup 137}Cs on the Ambiol and El dose was not proportional and the most significant decrease in the radionuclide uptake by plants was reported with the use of dose showing the most pronounced stimulating effect on the barley growth and development. The pre-sowing seed treatment with Ambiol increased Pb absorption by 35-50% and, on the contrary, decreased Cd uptake by plants by 30-40%. (authors)

Kruglov, Stanislav; Filipas, Alexander [Russian Institute of Agricultural Radiology and Agroecology, 249020 Obninsk (Russian Federation)

2007-07-01T23:59:59.000Z

149

Pilot-Scale Demonstration of Hybrid Zero-Valent Iron Water Treatment Technology: Removing Trace Metals from Flue Gas Desulfurization (FGD) Wastewater  

Science Conference Proceedings (OSTI)

In previous laboratory- and field bench-scale tests, the hybrid zero-valent iron (hZVI) process had been demonstrated capable of removing selenium, mercury, nitrates, and other pollutants from flue gas desulfurization (FGD) wastewater. By incorporating zero-valent iron (ZVI) with magnetite and certain Fe(II) species, the hZVI technology creates a highly reactive mixture that can transform and immobilize various trace metals, oxyanions, and other impurities from aqueous streams. To further evaluate ...

2013-04-09T23:59:59.000Z

150

Carcinogenic heavy metals replace Ca{sup 2+} for DNA binding and annealing activities of mono-ubiquitinated annexin A1 homodimer  

Science Conference Proceedings (OSTI)

Mono-ubiquitinated annexin A1 was purified from rat liver nuclei. The homodimer form of mono-ubiquitinated annexin A1 was able to unwind dsDNA in a Mg{sup 2+}- and ATP-dependent manner, and to anneal ssDNA in a Ca{sup 2+}-dependent manner. Phospholipids decreased the concentration of Ca{sup 2+} required for maximal annealing activity. Heavy metals such as As{sup 3+}, Cr{sup 6+}, Pb{sup 2+} and Cd{sup 2+} substituted for Ca{sup 2+} in the ssDNA binding and annealing activities of annexin A1. While these metals inhibited the unwinding of dsDNA by nuclear annexin A1 in the presence of Mg{sup 2+} and ATP, they enhanced dsDNA-dependent ATPase activity of annexin A1. Heavy metals may have produced dsDNA, a substrate for the DNA unwinding reaction, via the DNA annealing reaction. DNA synthesomes were isolated from L5178Y tk(+/-) mouse lymphoma cells in exponential growth, and were found to contain helicase activities. The As{sup 3+}- or Cr{sup 6+}-induced increases in ssDNA binding activity of DNA synthesomes were reduced by a mono-specific anti-annexin A1 antibody, but not by anti-Ig antibody. Anti-annexin A1 antibody also blocked the inhibitory and stimulatory effects of As{sup 3+} or Cr{sup 6+} towards DNA unwinding and annealing activities of DNA synthesomes. Based on these observations, it can be concluded that the effects of heavy metals on DNA annealing and unwinding activities are mediated, at least in substantial part, through actions of the mono-ubiquitinated annexin A1 homodimer.

Hirata, Aiko; Corcoran, George B.; Hirata, Fusao, E-mail: fhirata@wayne.ed

2010-10-01T23:59:59.000Z

151

Three dimensional electrode for the electrolytic removal of contaminants from aqueous waste streams  

DOE Patents (OSTI)

Efficient and cost-effective electrochemical devices and processes for the remediation of aqueous waste streams. The invention provides electrolytic cells having a high surface area spouted electrode for removal of heavy metals and oxidation of organics from aqueous environments. Heavy metal ions are reduced, deposited on cathode particles of a spouted bed cathode and removed from solution. Organics are efficiently oxidized at anode particles of a spouted bed anode and removed from solution. The method of this inventions employs an electrochemical cell having an anolyte compartment and a catholyte compartment, separated by a microporous membrane, in and through which compartments anolyte and catholyte, respectively, are circulated. A spouted-bed electrode is employed as the cathode for metal deposition from contaminated aqueous media introduced as catholyte and as the anode for oxidation of organics from contaminated aqueous media introduced as anolyte.

Spiegel, Ella F. (Louisville, CO); Sammells, Anthony F. (Boulder, CO)

2001-01-01T23:59:59.000Z

152

Effect of residual chips on the material removal process of the bulk metallic glass studied by in situ scratch testing inside the scanning electron microscope  

Science Conference Proceedings (OSTI)

Research on material removal mechanism is meaningful for precision and ultra-precision manufacturing. In this paper, a novel scratch device was proposed by integrating the parasitic motion principle linear actuator. The device has a compact structure and it can be installed on the stage of the scanning electron microscope (SEM) to carry out in situ scratch testing. Effect of residual chips on the material removal process of the bulk metallic glass (BMG) was studied by in situ scratch testing inside the SEM. The whole removal process of the BMG during the scratch was captured in real time. Formation and growth of lamellar chips on the rake face of the Cube-Corner indenter were observed dynamically. Experimental results indicate that when lots of chips are accumulated on the rake face of the indenter and obstruct forward flow of materials, materials will flow laterally and downward to find new location and direction for formation of new chips. Due to similar material removal processes, in situ scratch testing is potential to be a powerful research tool for studying material removal mechanism of single point diamond turning, single grit grinding, mechanical polishing and grating fabrication.

Huang Hu; Zhao Hongwei; Shi Chengli; Wu Boda; Fan Zunqiang; Wan Shunguang; Geng Chunyang [College of Mechanical Science and Engineering, Jilin University, Renmin Street 5988, Changchun, Jilin 130025 (China)

2012-12-15T23:59:59.000Z

153

Stabilization and reuse of heavy metal contaminated soils by means of quicklime sulfate salt treatment. Final report, September 1992--February 1995  

SciTech Connect

Capillary and hydraulic flows of water in porous media contaminated by heavy metal species often result in severe aquifer contamination. In the present study a chemical admixture stabilization approach is proposed, where heavy metal stabilization/immobilization is achieved by means of quicklime-based treatment. Both in-situ treatment by injection and on-site stabilization by excavation, mixing, and compaction will be investigated. In addition, the potential to reuse the resulting stabilized material as readily available construction material will also be investigated. The heavy metals under study include: arsenic, chromium, lead, and mercury. The proposed technical approach consists of three separate phases. During phase A, both artificial and naturally occurring contaminated soil mixes were treated, and then tested for stress-strain properties, leachability, micromorphology, mineralogical composition, permeability, setting time, and durability. In such a way, the effectiveness of the proposed remediation technology was verified, the treatment approach was optimized, and the underlying mechanisms responsible for stabilization were established. During phase B, the proposed technology will be tested for two DOE-site subscale systems, involving naturally occurring contaminated soil, using the same testing methodology as the one outlined for phase A. Provided that the proposed technology is proven effective for the subscale systems, a field application will be demonstrated. Again process quality monitoring will be performed by testing undisturbed samples collected from the treated sites, in the same fashion as for the previous phases. Following completion of the proposed study, a set of comprehensive guidelines for field applications will be developed. 42 refs., 196 figs., 26 tabs.

Dermatas, D.

1995-08-01T23:59:59.000Z

154

Investigation of methods for the selective removal and characterization of transition metals associated with solids in the marine environment  

DOE Green Energy (OSTI)

The operation of an OTEC plant will result in the mixing of large volumes of seawater from different depths within the ocean. Because suspended particulate material is intimately involved in marine food webs and transition metals, such as copper, can have toxic effects, it is important to develop a sound methodology for characterizing and quantifying transition metal behavior associated with the solid material. The characterization of solid-phase-associated transition metals in the marine environment has largely been directed at marine sediments. These studies have generally indicated that it is not possible to uniquely identify the solid phases or chemical speciation of a given metal. There are many reasons for this difficulty, but the probable major analytical problems arise from the fact that many of the transition metals of interest are present only in trace concentrations as adsorbed species on amorphous oxides or as coprecipitates. In one approach transition metals are classified according to how easily they are solubilized when exposed to different types of chemical attack, as defined in chemical extraction schemes. In this study, several of the most widely accepted extraction techniques were compared for many of the most commonly measured transition metals to a variety of marine sediments. Based on the results of this study, the sequential extraction scheme of Tessler et al. (1979) is the recommended method for the characterization of solid-phase associated transition metals. An increase of the reducing agent concentration in the intermediate step and temperature decrease with an additional HCl digestion in the residual step are recommended as improvements, based on the results of the individual extraction method studies.

Van Valin, R.; Morse, J.W.

1981-02-01T23:59:59.000Z

155

Polymer-supported sulfonated catechol and linear catechol amide ligands and their use in selective metal ion removal recovery from aqueous solutions  

DOE Patents (OSTI)

The present invention concerns the synthesis of several biomimetically important polymer-supported, sulfonated catechol (PS-CATS), sulfonated bis-catechol linear amide (PS-2-6-LICAMS) and sulfonated 3,3-linear tris-catechol amide (PS-3,3-LICAMS) ligands, which chemically bond to modified 6% crosslinked macroporous polystyrene-divinylbenzene beads (PS-DVB). These polymers are useful for the for selective removal and recovery of environmentally and economically important metal ions from aqueous solution, as a function of pH. The Fe.sup.3+ ion selectivity shown for PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads in competition with a similar concentration of Cu.sup.2+, Zn.sup.2+, Mn.sup.2+, Ni.sup.2+, Mg.sup.2+, Al.sup.3+, and Cr.sup.3+ ions at pH 1-3. Further, the metal ion selectivity is changed at higher pH values in the absence of Fe.sup.3+ (for example, Hg.sup.2+ at pH 3). The rates of selective removal and recovery of the trivalent metal ions, e.g. Fe.sup.3+ Al.sup.3+ ion etc. with the PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads used determined are useful as well as equilibrium selectivity coefficient (K.sub.m) values for all metal competition studies. The chelate effect for the predisposed octahedral PS-3,3-LICAMS polymer pendant ligand is the reason that this ligand has a more pronounced selectivity for Fe.sup.3+ ion in comparison to the PS-CATS polymer beads. The predisposed square planar PS-2,6-LICAMS series of polymer pendant ligands are more selective to divalent metal ions Cu.sup.2+, Zn.sup.2+, Mn.sup.2+, Ni.sup.2+, and Mg.sup.2+, than either PS-CATS or PS-3,3-LICAMS. However, Fe.sup.3+ ion still dominates in competition with other divalent and trivalent metal ions. In the absence of Fe.sup.3+, the polymer ligand is selective for Al.sup.3+, Cu.sup.2+ or Hg.sup.2+. The changing of the cavity size from two CH.sub.2 groups to six CH.sub.2 groups in the PS-2-6-LICAMS polymer pendant ligand series does not effect the order of metal ion selectivity.

Fish, Richard H. (Berkeley, CA)

1998-01-01T23:59:59.000Z

156

Polymer-supported sulfonated catechol and linear catechol amide ligands and their use in selective metal ion removal recovery from aqueous solutions  

DOE Patents (OSTI)

The present invention concerns the synthesis of several biomimetically important polymer-supported, sulfonated catechol (PS-CATS), sulfonated bis-catechol linear amide (PS-2-6-LICAMS) and sulfonated 3,3-linear tris-catechol amide (PS-3,3-LICAMS) ligands, which chemically bond to modified 6% crosslinked macroporous polystyrene-divinylbenzene beads (PS-DVB). These polymers are useful for the for selective removal and recovery of environmentally and economically important metal ions from aqueous solution, as a function of pH. The Fe{sup 3+} ion selectivity shown for PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads in competition with a similar concentration of Cu{sup 2+}, Zn{sup 2+}, Mn{sup 2+}, Ni{sup 2+}, Mg{sup 2+}, Al{sup 3+}, and Cr{sup 3+} ions at pH 1--3. Further, the metal ion selectivity is changed at higher pH values in the absence of Fe{sup 3+} (for example, Hg{sup 2+} at pH 3). The rates of selective removal and recovery of the trivalent metal ions, e.g. Fe{sup 3+}, Al{sup 3+} ion etc. with the PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads used determined are useful as well as equilibrium selectivity coefficient (K{sub m}) values for all metal competition studies. The chelate effect for the predisposed octahedral PS-3,3-LICAMS polymer pendant ligand is the reason that this ligand has a more pronounced selectivity for Fe{sup 3+} ion in comparison to the PS-CATS polymer beads. The predisposed square planar PS-2,6-LICAMS series of polymer pendant ligands are more selective to divalent metal ions Cu{sup 2+}, Zn{sup 2+}, Mn{sup 2+}, Ni{sup 2+}, and Mg{sup 2+}, than either PS-CATS or PS-3,3-LICAMS. However, Fe{sup 3+} ion still dominates in competition with other divalent and trivalent metal ions. In the absence of Fe{sup 3+}, the polymer ligand is selective for Al{sup 3+}, Cu{sup 2+} or Hg{sup 2+}. The changing of the cavity size from two CH{sub 2} groups to six CH{sub 2} groups in the PS-2-6-LICAMS polymer pendant ligand series does not effect the order of metal ion selectivity. 9 figs.

Fish, R.H.

1998-11-10T23:59:59.000Z

157

Polymer-supported sulfonated catechol and linear catechol amide ligands and their use in selective metal ion removal and recovery from aqueous solutions  

DOE Patents (OSTI)

The present invention concerns the synthesis of several biomimetically important polymer-supported, sulfonated catechol (PS-CATS), sulfonated bis-catechol linear amide (PS-2-6-LICAMS) and sulfonated 3,3-linear tris-catechol amide (PS-3,3-LICAMS) ligands, which chemically bond to modified 6% crosslinked macroporous polystyrene-divinylbenzene beads (PS-DVB). These polymers are useful for the for selective removal and recovery of environmentally and economically important metal ions from aqueous solution, as a function of pH. The Fe.sup.3+ ion selectivity shown for PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads in competition with a similar concentration of Cu.sup.2+, Zn.sup.2+, Mn.sup.2+, Ni.sup.2+,Mg.sup.2+, Al.sup.3+, and Cr.sup.3+ ions at pH 1-3. Further, the metal ion selectivity is changed at higher pH values in the absence of Fe.sup.3+ (for example, Hg.sup.2+ at pH 3). The rates of selective removal and recovery of the trivalent metal ions, e.g. Fe.sup.3+ Al.sup.3+ ion etc. with the PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads use determined are useful as well as equilibrium selectivity coefficient (K.sub.m) values for all metal competition studies. The chelate effect for the predisposed octahedral PS-3,3-LICAMS polymer pendant ligand is the reason that this ligand has a more pronounced selectivity for Fe.sup.3+ ion in comparison to the PS-CATS polymer beads. The predisposed square planar PS-2-6-Mn.sup.2+, Ni.sup.2+, and Mg.sup.2+, than either PS-CATS or PS-3,3-LICAMS. However, Fe.sup.3+ ion still dominates in competition with other divalent and trivalent metal ions. In the absence of Fe.sup.3+, the polymer ligand is selective for Al.sup.3+, Cu.sup.2+ or Hg.sup.2+. The changing of the cavity size from two CH.sub.2 groups to six CH.sub.2 groups in the PS-2-6-LICAMS polymer pendant ligand series does not effect the order of metal ion selectivity.

Fish, Richard H. (Berkeley, CA)

1997-01-01T23:59:59.000Z

158

Polymer-supported sulfonated catechol and linear catechol amide ligands and their use in selective metal ion removal and recovery from aqueous solutions  

DOE Patents (OSTI)

The present invention concerns the synthesis of several biomimetically important polymer-supported, sulfonated catechol (PS-CATS), sulfonated bis-catechol linear amide (PS-2-6-LICAMS) and sulfonated 3,3-linear tris-catechol amide (PS-3,3-LICAMS) ligands, which chemically bond to modified 6% crosslinked macroporous polystyrene-divinylbenzene beads (PS-DVB). These polymers are useful for the for selective removal and recovery of environmentally and economically important metal ions from aqueous solution, as a function of pH. The Fe{sup 3+} ion selectivity shown for PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads in competition with a similar concentration of Cu{sup 2+}, Zn{sup 2+}, Mn{sup 2+}, Ni{sup 2+}, Mg{sup 2+}, Al{sup 3+}, and Cr{sup 3+} ions at pH 1--3. Further, the metal ion selectivity is changed at higher pH values in the absence of Fe{sup 3+} (for example, Hg{sup 2+} at pH 3). The rates of selective removal and recovery of the trivalent metal ions, e.g. Fe{sup 3+}, Al{sup 3+} ion etc. with the PS-CATS, PS-2-6-LICAMS, and PS-3,3-LICAMS polymer beads use determined are useful as well as equilibrium selectivity coefficient (K{sub m}) values for all metal competition studies. The chelate effect for the predisposed octahedral PS-3,3-LICAMS polymer pendant ligand is the reason that this ligand has a more pronounced selectivity for Fe{sup 3+} ion in comparison to the PS-CATS polymer beads. The predisposed square planar PS-2-6-Mn{sup 2+}, Ni{sup 2+}, and Mg{sup 2+}, than either PS-CATS or PS-3,3-LICAMS. However, Fe{sup 3+} ion still dominates in competition with other divalent and trivalent metal ions. In the absence of Fe{sup 3+}, the polymer ligand is selective for Al{sup 3+}, Cu{sup 2+} or Hg{sup 2+}. The changing of the cavity size from two CH{sub 2} groups to six CH{sub 2} groups in the PS-2-6-LICAMS polymer pendant ligand series does not effect the order of metal ion selectivity. 9 figs.

Fish, R.H.

1997-04-22T23:59:59.000Z

159

In-situ method to remove iron and other metals from Solution in Groundwater down Gradient from Permeable Reactive Barrier  

DOE Patents (OSTI)

This invention is directed to a process for treating the flow of anaerobic groundwater through an aquifer with a primary treatment media, preferably iron, and then passing the treated groundwater through a second porous media though which an oxygenated gas is passed in order to oxygenate the dissolved primary treatment material and convert it into an insoluble material thereby removing the dissolved primary treatment material from the groundwater.

Carpenter, Clay E.; Morrison, Stanley J.

1999-09-22T23:59:59.000Z

160

In-situ method to remove iron and other metals from solution in groundwater down gradient from permeable reactive barrier  

DOE Patents (OSTI)

This invention is directed to a process for treating the flow of anaerobic groundwater through an aquifer with a primary treatment media, preferably iron, and then passing the treated groundwater through a second porous media though which an oxygenated gas is passed in order to oxygenate the dissolved primary treatment material and convert it into an insoluble material thereby removing the dissolved primary treatment material from the groundwater.

Carpenter, Clay E. (Grand Junction, CO); Morrison, Stanley J. (Grand Junction, CO)

2001-07-03T23:59:59.000Z

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they are not comprehensive nor are they the most current set.
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161

Continuous sulfur removal process  

DOE Patents (OSTI)

A continuous process for the removal of hydrogen sulfide from a gas stream using a membrane comprising a metal oxide deposited on a porous support is disclosed. 4 figures.

Jalan, V.; Ryu, J.

1994-04-26T23:59:59.000Z

162

HOW ENVIRONMENTAL RISK FROM LEACH ING OF HEAVY METALS IN ASH RESIDUES FROM COMBUSTION OF MUNIC IPAL SOLID WASTE  

E-Print Network (OSTI)

Laboratories which led to the use of acid tests such as the EP and TCLP tests. [25] 13 #12;CONCLUSIONS and soluble metals in the ash from Waste-to Energy (WTE) facilities has led to a public concern about why has led to the requirement for continuous monitoring of oxygen , carbon monoxide (CO) , and acid gases

Columbia University

163

Thermohydraulic investigations by decay heat removal systems; By natural convection for liquid-metal fast breeder reactors  

SciTech Connect

This paper reports, to examine the function of the safety-related SNR-2 decay heat removal concept, natural convection experiments performed in two-and three-dimensional water models, scaled 1:20, under conditions of symmetric and nonsymmetric loads of the immersed coolers installed in the upper plenum at 180-deg positions with respect to each other. The temperature and velocity distributions were measured and the flow patterns recorded for different configurations of the instrumented plug. For symmetric load conditions, symmetric temperature and flow distributions were measured in two- and three-dimensional models. Nonsymmetric load conditions produce remarkable temperature differences between the two separated plenums of the two-dimensional model if fluid circulation is suppressed by a closed plug. An open plug allows fluid to pass through and shows lower temperature differences. In contrast, in the three-dimensional experiment, azimuthal fluid flow inside the plenum prevails even with the plug closed, and identical temperature distributions are measured. The calculations using the COMMIX-1B code are generally in good agreement with the measurements.

Hoffmann, H.; Weinberg, D. (Kernforschungszentrum Karlsruhe GmbH Institut fur Reaktorbaulemente, Postfach 3640, 7500 Karsruhe 1 (DE)); Ieday (Power Reactor and Nuclear Fuel Development Corporation Oarai Engineering Center, Oarai (JP)); Martex, K.; Tschoke, H.H.; Dres, K. (Kernforschungszentrum Karlsruhe GmbH, Institut fur Reaktorbauelemente, Postfach 3640, 7500 Karlsruhe 1 (DE))

1989-10-01T23:59:59.000Z

164

Association of the sites of heavy metals with nanoscale carbon in a Kentucky electrostatic precipitator fly ash  

Science Conference Proceedings (OSTI)

A combination of high-resolution transmission electron microscopy, scanning transmission electron microscopy, and electron energy-loss spectroscopy (HRTEM-STEM-EELS) was used to study fly ashes produced from the combustion of an eastern Kentucky coal at a southeastern-Kentucky wall-fired pulverized coal utility boiler retrofitted for low-NOx combustion. Fly ash was collected from individual hoppers in each row of the electrostatic precipitators (ESP) pollution-control system, with multiple hoppers sampled within each of the three rows. Temperatures within the ESP array range from about 200 {degree}C at the entry to the first row to <150{degree}C at the exit of the third row. HRTEM-STEM-EELS study demonstrated the presence of nanoscale (10 s nm) C agglomerates with typical soot-like appearance and others with graphitic fullerene-like nanocarbon structures. The minute carbon agglomerates are typically juxtaposed and intergrown with slightly larger aluminosilicate spheres and often form an ultrathin halo or deposit on the fly ash particles. The STEM-EELS analyses revealed that the nanocarbon agglomerates host even finer (<3 nm) metal and metal oxide particles. Elemental analysis indicated an association of Hg with the nanocarbon. Arsenic, Se, Pb, Co, and traces of Ti and Ba are often associated with Fe-rich particles within the nanocarbon deposits. 57 refs., 5 figs.

James C. Hower; Uschi M. Graham; Alan Dozier; Michael T. Tseng; Rajesh A. Khatri [University of Kentucky, Lexington, KY (United States). Center for Applied Energy Research

2008-11-15T23:59:59.000Z

165

The Affect of the Hydrogen to Heavy Metal Ratio (H/HM) on Reactivity and Discharge Isotopics of Homogeneous Thoria-Urania Fuel  

DOE Green Energy (OSTI)

Calculations were performed using MOCUP, which includes the use of MCNP for neutron transport and ORIGEN for depletion. The MOCUP calculations were done using a unit cell (pin cell) model, where the ThO2 varied from 65-75wt% and the UO2 varied from 25-35wt%. The fission products and actinides being tracked in the calculations account for >97% of the parasitic captures in the fuel. The fuel pin was surrounded by four reflecting planes, where typical parameters were used for a 17x17 PWR assembly. The hydrogen to heavy metal ratio (H/HM) was varied by increasing or decreasing the water density in the cell. The results show that the drier lattices have insufficient reactivity due to the limited enrichment of the uranium. However, a slightly wetter lattice will increase the reactivity-limited burnup by 26% for the 25% UO2 – 75% ThO2, and 19% for the 35% UO2 – 65% ThO2 as compared to the standard coolant density. This is appears to be consistent with similar studies done with all-uranium lattices, where advantages are gained by hardening or further softening the neutron spectrum. Although some advantage is gained by softening the spectrum, the same can be said of all-uranium fueled cores. The spectral changes and, to a lesser extent, competing resonances between the 238U and bred-in 233U appear to hamper advantages in the conversion of thorium in homogeneous fuel that might otherwise be gained by shifting the neutron spectrum. Physically separating the uranium and thorium (e.g., in micro-heterogeneous and seed-and-blanket arrangements) have been shown alleviate this problem. A change in moderation may further enhance the reactivity-limited burnup of these lattices, and will be the focus of future work.

Weaver, Kevan Dean; Herring, James Stephen

2002-04-01T23:59:59.000Z

166

Polymer pendant ligand chemistry. 3. A biomimetic approach to selective metal ion removal and recovery from aqueous solution with polymer-supported sulfonated catechol and linear catechol amide ligands  

Science Conference Proceedings (OSTI)

The design of organic ligands to selectively remove and recover metal ions from aqueous solution is a new and important area of environmental inorganic chemistry. One approach to designing organic ligands for these purposes is to use biological systems as examples for selective metal ion complexation. Thus, the authors report results on the synthesis of several biomimetically important polymer-supported, sulfonated catechol (PS-CATS), sulfonated bis(catechol) linear amide (PS-2-6-LICAMS), and sulfonated 3.3-linear tris(catechol) amide (PS-3,3-LICAMS) ligands that are chemically bonded to modified 6% cross-linked macroporous polystyrene-divinylbenzene beads (PS-DVB) for selective removal and recovery of environmentally and economically important metal ions from aqueous solution, as a function of pH. The Fe{sup 3+} ion selectivity was dramatically shown for PS-CATS, PS-2-6-LICAMS and PS-3,3-LICAMS polymer beads in competition with a similar concentration of Cu{sup 2+}, Zn{sup 2+}, Mn{sup 2+}, Ni{sup 2+}, Mg{sup 2+}, Al{sup 3+}, and Cr{sup 3+} ions at pH 1-3, while metal ion selectivity could be changed at higher pH values in the absence of Fe{sup 3+} (for example, Hg{sup 2+} at pH 3). Rates of removal and recovery of the Fe{sup 3+} ion with the PS-CATS, PS-2-6LICAMS and PS-3,3-LICAMS polymer beads were also studied as well as relative equilibrium selectivity coefficient (K{sub m}) values for all metal competition studies.

Huang, Song-Ping; Li, Wei; Franz, K.J.; Albright, R.L.; Fish, R.H. [Univ. of California, Berkeley, CA (United States)

1995-05-24T23:59:59.000Z

167

FORMING PROTECTIVE FILMS ON METAL  

DOE Patents (OSTI)

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

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

1958-12-16T23:59:59.000Z

168

Removal of Fluoride from Waste Water of Aluminium Smelter by ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2011 TMS Annual Meeting & Exhibition. Symposium , General Abstracts: Light Metals Division. Presentation Title, Removal of ...

169

Powder Removal from Complex Structures Produced Using Electron ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, Materials Science & Technology 2011. Symposium, Additive Manufacturing of Metals. Presentation Title, Powder Removal from ...

170

Economic feasibility of biochemical processes for the upgrading of crudes and the removal of sulfur, nitrogen, and trace metals from crude oil -- Benchmark cost establishment of biochemical processes on the basis of conventional downstream technologies. Final report FY95  

Science Conference Proceedings (OSTI)

During the past several years, a considerable amount of work has been carried out showing that microbially enhanced oil recovery (MEOR) is promising and the resulting biotechnology may be deliverable. At Brookhaven National Laboratory (BNL), systematic studies have been conducted which dealt with the effects of thermophilic and thermoadapted bacteria on the chemical and physical properties of selected types of crude oils at elevated temperatures and pressures. Current studies indicate that during the biotreatment several chemical and physical properties of crude oils are affected. The oils are (1) emulsified; (2) acidified; (3) there is a qualitative and quantitative change in light and heavy fractions of the crudes; (4) there are chemical changes in fractions containing sulfur compounds; (5) there is an apparent reduction in the concentration of trace metals; and (6) the qualitative and quantitative changes appear to be microbial species dependent; and (7) there is a distinction between biodegraded and biotreated oils. The downstream biotechnological crude oil processing research performed thus far is of laboratory scale and has focused on demonstrating the technical feasibility of downstream processing with different types of biocatalysts under a variety of processing conditions. Quantitative economic analysis is the topic of the present project which investigates the economic feasibility of the various biochemical downstream processes which hold promise in upgrading of heavy crudes, such as those found in California, e.g., Monterey-type, Midway Sunset, Honda crudes, and others.

Premuzic, E.T.

1996-08-01T23:59:59.000Z

171

Heavy Oil Projects  

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

Select Reports from Heavy Oil Projects Project Number Performer Title Heavy Oil Recovery US (NIPERBDM-0225) BDM-Oklahoma, Inc. Feasibility Study of Heavy Oil Recovery in the...

172

Extracting metals directly from metal oxides  

DOE Patents (OSTI)

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

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

1997-01-01T23:59:59.000Z

173

Extracting metals directly from metal oxides  

DOE Patents (OSTI)

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

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

1997-02-25T23:59:59.000Z

174

Multiple pollutant removal using the condensing heat exchanger. Task 2, Pilot scale IFGT testing  

Science Conference Proceedings (OSTI)

The purpose of Task 2 (IFGT Pilot-Scale Tests at the B&W Alliance Research Center) is to evaluate the emission reduction performance of the Integrated flue Gas Treatment (IFGT) process for coal-fired applications. The IFGT system is a two-stage condensing heat exchanger that captures multiple pollutants - while recovering waste heat. The IFGT technology offers the potential of a addressing the emission of SO{sub 2} and particulate from electric utilities currently regulated under the Phase I and Phase II requirements defined in Title IV, and many of the air pollutants that will soon be regulated under Title III of the Clean Air Act. The performance data will be obtained at pilot-scale conditions similar to full-scale operating systems. The task 2 IFGT tests have been designed to investigate several aspects of IFGT process conditions at a broader range of variable than would be feasible at a larger scale facility. The performance parameters that will be investigated are as follows: SO{sub 2} removal; particulate removal; removal of mercury and other heavy metals; NO{sub x} removal; HF and HCl removal; NH{sub 3} removal; ammonia-sulfur compounds generation; and steam injection for particle removal. For all of the pollutant removal tests, removal efficiency will be based on measurements at the inlet and outlet of the IFGT facility. Heat recovery measurements will also be made during these tests to demonstrate the heat recovery provided by the IFGT technology. This report provides the Final Test Plan for the first coal tested in the Task 2 pilot-scale IFGT tests.

Jankura, B.J.

1996-01-01T23:59:59.000Z

175

Laser removal of sludge from steam generators  

SciTech Connect

A method of removing unwanted chemical deposits known as sludge from the metal surfaces of steam generators with laser energy is provided. Laser energy of a certain power density, of a critical wavelength and frequency, is intermittently focused on the sludge deposits to vaporize them so that the surfaces are cleaned without affecting the metal surface (sludge substrate). Fiberoptic tubes are utilized for laser beam transmission and beam direction. Fiberoptics are also utilized to monitor laser operation and sludge removal.

Nachbar, Henry D. (Ballston Lake, NY)

1990-01-01T23:59:59.000Z

176

Heavy Vehicle Propulsion Materials Program  

DOE Green Energy (OSTI)

The objective of the Heavy Vehicle Propulsion Materials Program is to develop the enabling materials technology for the clean, high-efficiency diesel truck engines of the future. The development of cleaner, higher-efficiency diesel engines imposes greater mechanical, thermal, and tribological demands on materials of construction. Often the enabling technology for a new engine component is the material from which the part can be made. The Heavy Vehicle Propulsion Materials Program is a partnership between the Department of Energy (DOE), and the diesel engine companies in the United States, materials suppliers, national laboratories, and universities. A comprehensive research and development program has been developed to meet the enabling materials requirements for the diesel engines of the future. Advanced materials, including high-temperature metal alloys, intermetallics, cermets, ceramics, amorphous materials, metal- and ceramic-matrix composites, and coatings, are investigated for critical engine applications.

Sidney Diamond; D. Ray Johnson

1999-04-26T23:59:59.000Z

177

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, M.; Sinha, S.N.

1987-07-30T23:59:59.000Z

178

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, M.; Sinha, S.N.

1990-05-15T23:59:59.000Z

179

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, Milton (12833 S. 82nd Ct., Palos Park, IL 60464); Sinha, Shome N. (5748 Drexel, 2A, Chicago, IL 60637)

1990-01-01T23:59:59.000Z

180

Process for removing pyritic sulfur from bituminous coals  

DOE Patents (OSTI)

A process is provided for removing pyritic sulfur and lowering ash content of bituminous coals by grinding the feed coal, subjecting it to micro-agglomeration with a bridging liquid containing heavy oil, separating the microagglomerates and separating them to a water wash to remove suspended pyritic sulfur. In one embodiment the coal is subjected to a second micro-agglomeration step.

Pawlak, Wanda (Edmonton, CA); Janiak, Jerzy S. (Edmonton, CA); Turak, Ali A. (Edmonton, CA); Ignasiak, Boleslaw L. (Edmonton, CA)

1990-01-01T23:59:59.000Z

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181

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

182

Alkali metal nitrate purification  

DOE Patents (OSTI)

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

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

1986-02-04T23:59:59.000Z

183

PROCESS FOR REMOVING NOBLE METALS FROM URANIUM  

DOE Patents (OSTI)

A pyrometallurgical method is given for purifying uranium containing ruthenium and palladium. The uranium is disintegrated and oxidized by exposure to air and then the ruthenium and palladium are extracted from the uranium with molten zinc.

Knighton, J.B.

1961-01-31T23:59:59.000Z

184

HEAVY-ION RADIOGRAPHY AND HEAVY-ION COMPUTED TOMOGRAPHY  

E-Print Network (OSTI)

In: Biological and Medical Research with Accelerated Heavyeds. Biological and Medical Research with Accelerated HeavyIn: Biological and Medical Research with Accelerated Heavy

Fabrikant, J.I.

2010-01-01T23:59:59.000Z

185

METHOD OF OPERATING A HEAVY WATER MODERATED REACTOR  

DOE Patents (OSTI)

A method of removing fission products from the heavy water used in a slurry type nuclear reactor is described. According to the process the slurry is steam distilled with carbon tetrachloride so that at least a part of the heavy water and carbon tetrachloride are vaporized; the heavy water and carbon tetrachloride are separated; the carbon tetrachloride is returned to the steam distillation column at different points in the column to aid in depositing the slurry particles at the bottom of the column; and the heavy water portion of the condensate is purified. (AEC)

Vernon, H.C.

1962-08-14T23:59:59.000Z

186

Pipelineable syncrude (synthetic crude) from heavy oil  

SciTech Connect

This patent describes a process for converting a metals-contaminated heavy crude oil characterized by an API gravity less than about 20{degrees} and a substantial Conradson Carbon Residue to a pipelineable and substantially upgraded syncrude with concomitant recovery of blown asphalt. It comprises: air-blowing at least the 650{degrees} F.{sup +} fraction of the heavy crude oil at a temperature of 390{degrees} to 600{degrees} F. under conditions effective to increase its combined oxygen content by at least 0.5 weight percent; deasphalting the air-blown crude oil with solvent whereby separately recovering a blown asphalt and an intermediate syncrude having a substantially lower concentration of metals and less Conradson Carbon residue than the heavy crude oil; and, visbreaking the intermediate syncrude at 800{degrees} to 950{degrees} F. and at a severity effective to impart to it pipelineable viscosity characteristics.

Rankel, L.A.

1989-06-12T23:59:59.000Z

187

Reversible photodeposition and dissolution of metal ions  

DOE Patents (OSTI)

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

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

1994-01-01T23:59:59.000Z

188

Method for the removal and recovery of mercury  

DOE Patents (OSTI)

The present invention is an enhanced method for the removal and recovery of mercury from mercury-contaminated matrices. The method involves contacting a mercury-contaminated matrix with an aqueous dispersant solution derived from specific intra-amoebic isolates to release the mercury from the mercury-contaminated matrix and emulsify the mercury; then, contacting the matrix with an amalgamating metal from a metal source to amalgamate the mercury to the amalgamating metal; removing the metallic source from the mercury-contaminated matrix; and heating the metallic source to vaporize the mercury in a closed system to capture the mercury vapors.

Easterly, C.E.; Vass, A.A.; Tyndall, R.L.

1997-01-28T23:59:59.000Z

189

Method for the removal and recovery of mercury  

DOE Patents (OSTI)

The present invention is an enhanced method for the removal and recovery of mercury from mercury-contaminated matrices. The method involves contacting a mercury-contaminated matrix with an aqueous dispersant solution derived from specific intra-amoebic isolates to release the mercury from the mercury-contaminated matrix and emulsify the mercury; then, contacting the matrix with an amalgamating metal from a metal source to amalgamate the mercury to the amalgamating metal; removing the metallic source from the mercury-contaminated matrix; and heating the metallic source to vaporize the mercury in a closed system to capture the mercury vapors.

Easterly, Clay E. (Knoxville, TN); Vass, Arpad A. (Oak Ridge, TN); Tyndall, Richard L. (Clinton, TN)

1997-01-01T23:59:59.000Z

190

Sovent Based Enhanced Oil Recovery for In-Situ Upgrading of Heavy Oil Sands  

Science Conference Proceedings (OSTI)

With the depletion of conventional crude oil reserves in the world, heavy oil and bitumen resources have great potential to meet the future demand for petroleum products. However, oil recovery from heavy oil and bitumen reservoirs is much more difficult than that from conventional oil reservoirs. This is mainly because heavy oil or bitumen is partially or completely immobile under reservoir conditions due to its extremely high viscosity, which creates special production challenges. In order to overcome these challenges significant efforts were devoted by Applied Research Center (ARC) at Florida International University and The Center for Energy Economics (CEE) at the University of Texas. A simplified model was developed to assess the density of the upgraded crude depending on the ratio of solvent mass to crude oil mass, temperature, pressure and the properties of the crude oil. The simplified model incorporated the interaction dynamics into a homogeneous, porous heavy oil reservoir to simulate the dispersion and concentration of injected CO{sub 2}. The model also incorporated the characteristic of a highly varying CO{sub 2} density near the critical point. Since the major challenge in heavy oil recovery is its high viscosity, most researchers have focused their investigations on this parameter in the laboratory as well as in the field resulting in disparaging results. This was attributed to oil being a complex poly-disperse blend of light and heavy paraffins, aromatics, resins and asphaltenes, which have diverse behaviors at reservoir temperature and pressures. The situation is exacerbated by a dearth of experimental data on gas diffusion coefficients in heavy oils due to the tedious nature of diffusivity measurements. Ultimately, the viscosity and thus oil recovery is regulated by pressure and its effect on the diffusion coefficient and oil swelling factors. The generation of a new phase within the crude and the differences in mobility between the new crude matrix and the precipitate readily enables removal of asphaltenes. Thus, an upgraded crude low in heavy metal, sulfur and nitrogen is more conducive for further purification.

Norman Munroe

2009-01-30T23:59:59.000Z

191

Treatment of Heavy Metal Wastes II - TMS  

Science Conference Proceedings (OSTI)

Session Chairs: P.R. Khangaonkar, School of Materials and Minerals Engineering, Universiti Sains Malaysia, Perak Campus, Tronoh 31750, Malaysia; Co-chair: ...

192

PROCESS FOR THE SEPARATION OF HEAVY METALS  

DOE Patents (OSTI)

A method is presented for thc separation of plutonium from uranium and the fission products with which it is associated. The method is based on the fact that hexavalent plutonium forms an insoluble complex precipitate with sodium acetate, as does the uranyl ion, while reduced plutonium is not precipitated by sodium acetate. Several embodiments are shown, e.g., a solution containing plutonium and uranium in the hexavalent state may be contacted with sodium acetate causing the formation of a sodium uranyl acetate precipitate which carries the plutonium values while the fission products remain in solution. If the original solution is treated with a reducing agent, so that the plutonium is reduced while the uranium remains in the hexavalent state, and sodium and acetate ions are added, the uranium will precipitutc while the plutonium remains in solution effecting separation of the Pu from urarium.

Gofman, J.W.; Connick, R.E.; Wahl, A.C.

1959-01-27T23:59:59.000Z

193

Block Heavy Hitters  

E-Print Network (OSTI)

e study a natural generalization of the heavy hitters problem in thestreaming context. We term this generalization *block heavy hitters* and define it as follows. We are to stream over a matrix$A$, and report all *rows* ...

Andoni, Alexandr

2008-05-02T23:59:59.000Z

194

Heavy Squarks at the LHC  

E-Print Network (OSTI)

The LHC, with its seven-fold increase in energy over the Tevatron, is capable of probing regions of SUSY parameter space exhibiting qualitatively new collider phenomenology. Here we investigate one such region in which first generation squarks are very heavy compared to the other superpartners. We find that the production of these squarks, which is dominantly associative, only becomes rate-limited at mSquark > 4(5) TeV for L~10(100) fb-1. However, discovery of this scenario is complicated because heavy squarks decay primarily into a jet and boosted gluino, yielding a dijet-like topology with missing energy (MET) pointing along the direction of the second hardest jet. The result is that many signal events are removed by standard jet/MET anti-alignment cuts designed to guard against jet mismeasurement errors. We suggest replacing these anti-alignment cuts with a measurement of jet substructure that can significantly extend the reach of this channel while still removing much of the background. We study a selection of benchmark points in detail, demonstrating that mSquark= 4(5) TeV first generation squarks can be discovered at the LHC with L~10(100)fb-1.

JiJi Fan; David Krohn; Pablo Mosteiro; Arun M. Thalapillil; Lian-Tao Wang

2011-02-01T23:59:59.000Z

195

Characterization of Minerals, Metals, and Materials (Electronic Format)  

Science Conference Proceedings (OSTI)

May 1, 2007 ... 133-136]The Leaching Behavior of Heavy Metals in MSWI Bottom Ash by Carbonation Reaction with Diffeent Water Content[pp.

196

Process for removing mercury from aqueous solutions  

DOE Patents (OSTI)

A process for removing mercury from water to a level not greater than two parts per billion wherein an anion exchange material that is insoluble in water is contacted first with a sulfide containing compound and second with a compound containing a bivalent metal ion forming an insoluble metal sulfide. To this treated exchange material is contacted water containing mercury. The water containing not more than two parts per billion of mercury is separated from the exchange material.

Googin, John M. (Oak Ridge, TN); Napier, John M. (Oak Ridge, TN); Makarewicz, Mark A. (Knoxville, TN); Meredith, Paul F. (Knoxville, TN)

1986-01-01T23:59:59.000Z

197

Process for removing mercury from aqueous solutions  

DOE Patents (OSTI)

A process for removing mercury from water to a level not greater than two parts per billion wherein an anion exchange material that is insoluble in water is contacted first with a sulfide containing compound and second with a compound containing a bivalent metal ion forming an insoluble metal sulfide. To this treated exchange material is contacted water containing mercury. The water containing not more than two parts per billion of mercury is separated from the exchange material.

Googin, J.M.; Napier, J.M.; Makarewicz, M.A.; Meredith, P.F.

1985-03-04T23:59:59.000Z

198

METHOD OF PURIFYING URANIUM METAL  

DOE Patents (OSTI)

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

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

1958-12-23T23:59:59.000Z

199

Lithium metal reduction of plutonium oxide to produce plutonium metal  

DOE Patents (OSTI)

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

Coops, Melvin S. (Livermore, CA)

1992-01-01T23:59:59.000Z

200

Recovery and removal of mercury from mixed wastes. Final report, September 1994--June 1995  

SciTech Connect

In recognition of the major environmental problem created by mercury contamination of wastes and soils at an estimated 200,000 sites along US natural gas and oil pipelines and at a number of government facilities, including Oak Ridge, Savannah River, Hanford, and Rocky Flats, the US Department of Energy (DOE) is seeking an effective and economical process for removing mercury from various DOE waste streams in order to allow the base waste streams to be treated by means of conventional technologies. In response to the need for Unproved mercury decontamination technology, Mercury Recovery Services (MRS) has developed and commercialized a thermal treatment process for the recovery of mercury from contaminated soils and industrial wastes. The objectives of this program were to: demonstrate the technical and economic feasibility of the MRS process to successfully remove and recover mercury from low-level mixed waste containing mercury compounds (HgO, HgS, HgCl{sub 2}) and selected heavy metal compounds (PbO, CdO); determine optimum processing conditions required to consistently reduce the residual total mercury content to 1 mg/kg while rendering the treated product nontoxic as determined by TCLP methods; and provide an accurate estimate of the capital and operating costs for a commercial processing facility designed specifically to remove and recovery mercury from various waste streams of interest at DOE facilities. These objectives were achieved in a four-stage demonstration program described within with results.

Sutton, W.F.; Weyand, T.E.; Koshinski, C.J.

1995-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Turbomachinery debris remover  

DOE Patents (OSTI)

An apparatus for removing debris from a turbomachine. The apparatus includes housing and remotely operable viewing and grappling mechanisms for the purpose of locating and removing debris lodged between adjacent blades in a turbomachine.

Krawiec, Donald F. (Pittsburgh, PA); Kraf, Robert J. (North Huntingdon, PA); Houser, Robert J. (Monroeville, PA)

1988-01-01T23:59:59.000Z

202

Definition of heavy oil and natural bitumen  

Science Conference Proceedings (OSTI)

Definition and categorization of heavy oils and natural bitumens are generally based on physical or chemical attributes or on methods of extraction. Ultimately, the hydrocarbon's chemical composition will govern both its physical state and the extraction technique applicable. These oils and bitumens closely resemble the residuum from wholecrude distillation to about 1,000/degree/F; if the residuum constitutes at least 15% of the crude, it is considered to be heavy. In this material is concentrated most of the trace elements, such as sulfur, oxygen, and nitrogen, and metals, such as nickel and vanadium. A widely used definition separates heavy oil from natural bitumen by viscosity, crude oil being less, and bitumen more viscous than 10,000 cp. Heavy crude then falls in the range 10/degree/-20/degree/ API inclusive and extra-heavy oil less than 10/degree/ API. Most natural bitumen is natural asphalt (tar sands, oil sands) and has been defined as rock containing hydrocarbons more viscous than 10,000 cp or else hydrocarbons that may be extracted from mined or quarried rock. Other natural bitumens are solids, such as gilsonite, grahamite, and ozokerite, which are distinguished by streak, fusibility, and solubility. The upper limit for heavy oil may also be set at 18/degree/ API, the approximate limit for recovery by waterflood.

Meyer, R.F.

1988-08-01T23:59:59.000Z

203

Graphitic packing removal tool  

DOE Patents (OSTI)

Graphitic packing removal tools are described for removal of the seal rings in one piece from valves and pumps. The packing removal tool has a cylindrical base ring the same size as the packing ring with a surface finish, perforations, knurling or threads for adhesion to the seal ring. Elongated leg shanks are mounted axially along the circumferential center. A slit or slits permit insertion around shafts. A removal tool follower stabilizes the upper portion of the legs to allow a spanner wrench to be used for insertion and removal.

Meyers, K.E.; Kolsun, G.J.

1996-12-31T23:59:59.000Z

204

Building Removal Ongoing at DOE's Paducah Site | Department of Energy  

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

Building Removal Ongoing at DOE's Paducah Site Building Removal Ongoing at DOE's Paducah Site Building Removal Ongoing at DOE's Paducah Site August 23, 2012 - 12:00pm Addthis Media Contact Buz Smith Robert.Smith@lex.doe.gov 270-441-6821 PADUCAH, KY - Work is ongoing at the Paducah Gaseous Diffusion Plant (PGDP) to raze a 65,000-square-foot facility known as the C-340 Metals Plant, which was used to make uranium metal during the Cold War. Department of Energy (DOE) cleanup contractor LATA Environmental Services of Kentucky began removing more than 1,500 panels of cement-asbestos siding from the Metals Plant complex Wednesday in anticipation of New Jersey-based LVI Services starting demolition Sept. 19. Demolition work is projected to last through the end of calendar 2012. "This is an important milestone because the C-340 Metals Plant is the

205

SURFACE TREATMENT OF METALLIC URANIUM  

DOE Patents (OSTI)

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

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

1958-05-27T23:59:59.000Z

206

Thiacrown polymers for removal of mercury from waste streams  

DOE Patents (OSTI)

Thiacrown polymers immobilized to a polystyrene-divinylbenzene matrix react with Hg.sup.2+ under a variety of conditions to efficiently and selectively remove Hg.sup.2+ ions from acidic aqueous solutions, even in the presence of a variety of other metal ions. The mercury can be recovered and the polymer regenerated. This mercury removal method has utility in the treatment of industrial wastewater, where a selective and cost-effective removal process is required.

Baumann, Theodore F. (Tracy, CA); Reynolds, John G. (San Ramon, CA); Fox, Glenn A. (Livermore, CA)

2002-01-01T23:59:59.000Z

207

How to treat and recycle heavy clear brine fluids  

Science Conference Proceedings (OSTI)

Clear brine fluids, such as CaCl/sub 2/, are replacing muds in well completions and workovers. These ''solids-free'' fluids have caused increases in well productivity of as much as 850%. To use the fluids in higher density ranges, it is necessary to blend the CaCl/sub 2/ brines with the more expensive bromide fluids. This, in turn, has increased the importance of reclaiming weighted brines to make their use more cost effective. To reclaim clear fluids, the solids picked up during use are removed and the fluid is reused or reweighted. A common problem though is the post-precipitation of dissolved contaminants that may appear in the used brines after several days or weeks in storage. Precipitation also may occur if other heavy fluids are added to adjust density before reuse. Laboratory tests have identified the solids as primarily iron hydroxides and halides. (Halides are salts containing a halogen-flourine, chlorine, bromine, or iodine.) Additional experimentation has shown that pH adjustment at the well site or before transfer to storage facilities can provide a simple and effective way of controlling the precipitation of metal hydroxides and halides. This article discusses methods of pH control, measurement, and adjustment, which will allow for optimum use of clear brine fluids.

Pasztor, A.J.; Snover, J.S.

1983-07-01T23:59:59.000Z

208

Device for removing blackheads  

DOE Patents (OSTI)

A device for removing blackheads from pores in the skin having a elongated handle with a spoon shaped portion mounted on one end thereof, the spoon having multiple small holes piercing therethrough. Also covered is method for using the device to remove blackheads.

Berkovich, Tamara (116 N. Wetherly Dr., Suite 115, Los Angeles, CA)

1995-03-07T23:59:59.000Z

209

Synthetic and structural studies of linear bis-catechol amide, N,N{prime}-bis(2,3-dihydroxybenzoyl)-1,7-diazaheptane (5-LICAM), and its complexes with Ni{sup 2+} and Co{sup 2+}: Utilization of a polymer-supported, sulfonated analog, 5-LICAMS, as a biomimetic ligand for divalent metal ion removal from aqueous solution  

Science Conference Proceedings (OSTI)

The synthesis and structural characterization of the linear bis(catechol) amide ligand, N,N{prime}-bis(2,3-dihydroxy-benzoyl)-1.7-diazaheptane (5-LICAM, 1), was studied along with several metal complexes, namely, Ni{sup 2+} and Co{sup 2+}. In order to test the utilization of 1 in removing Ni{sup 2+} from aqueous solution for environmental inorganic applications, the authors synthesized the polymer pendant ligand version, PS-5-LICAM, bonded to modified 6% macroporous divinylbenzene-polystyrene beads (0.55 mmol/g), with an important modification of a sulfonate group on the catechol ring, PS-5-LICAMS, to impart hydrophilicity to the ligand site. Indeed, it was found that the PS-5-LICAMS ligand removed 0.35 mmol of Ni/g of polymer beads from aqueous solution at pH 2.5, but unfortunately, was not selective to Ni{sup 2+} in competition with other divalent metal ions. An in depth discussion of the X-ray structure of ligand 2 and that of the Ni complex, 3, will be presented.

Huang, Song-Ping, Franz, K.J.; Fish, R.H. [Lawrence Berkeley Lab., CA (United States); Olmstead, M.M. [Univ. of California, Davis, CA (United States)

1995-05-24T23:59:59.000Z

210

SUPRI heavy oil research program  

SciTech Connect

The 14th Annual Report of the SUPRI Heavy Oil Research Program includes discussion of the following topics: (1) A Study of End Effects in Displacement Experiments; (2) Cat Scan Status Report; (3) Modifying In-situ Combustion with Metallic Additives; (4) Kinetics of Combustion; (5) Study of Residual Oil Saturation for Steam Injection and Fuel Concentration for In-Situ Combustion; (6) Analysis of Transient Foam Flow in 1-D Porous Media with Computed Tomography; (7) Steam-Foam Studies in the Presence of Residual Oil; (8) Microvisualization of Foam Flow in a Porous Medium; (9) Three- Dimensional Laboratory Steam Injection Model; (10) Saturation Evaluation Following Water Flooding; (11) Numerical Simulation of Well-to-Well Tracer Flow Test with Nonunity Mobility Ratio.

Aziz, K.; Ramey, H.J. Jr.; Castanier, L.M.

1991-12-01T23:59:59.000Z

211

Preliminary Evaluation of Removing Used Nuclear Fuel From Nine Shutdown Sites  

SciTech Connect

he Blue Ribbon Commission on America’s Nuclear Future identified removal of stranded used nuclear fuel at shutdown sites as a priority so that these sites may be completely decommissioned and put to other beneficial uses. In this report, a preliminary evaluation of removing used nuclear fuel from nine shutdown sites was conducted. The shutdown sites included Maine Yankee, Yankee Rowe, Connecticut Yankee, Humboldt Bay, Big Rock Point, Rancho Seco, Trojan, La Crosse, and Zion. At these sites a total of 7649 used nuclear fuel assemblies and a total of 2813.2 metric tons heavy metal (MTHM) of used nuclear fuel are contained in 248 storage canisters. In addition, 11 canisters containing greater-than-Class C (GTCC) low-level radioactive waste are stored at these sites. The evaluation was divided in four components: • characterization of the used nuclear fuel and GTCC low-level radioactive waste inventory at the shutdown sites • an evaluation of the onsite transportation conditions at the shutdown sites • an evaluation of the near-site transportation infrastructure and experience relevant to the shipping of transportation casks containing used nuclear fuel from the shutdown sites • an evaluation of the actions necessary to prepare for and remove used nuclear fuel and GTCC low-level radioactive waste from the shutdown sites. Using these evaluations the authors developed time sequences of activities and time durations for removing the used nuclear fuel and GTCC low-level radioactive waste from a single shutdown site, from three shutdown sites located close to each other, and from all nine shutdown sites.

Maheras, Steven J.; Best, Ralph; Ross, Steven B.; Buxton, Kenneth A.; England, Jeffery L.; McConnell, Paul

2013-04-30T23:59:59.000Z

212

Tritium emission reduction at Darlington tritium removal facility using a Bubbler System  

SciTech Connect

Ontario Power Generation Nuclear (OPGN) has a 4 x 880 MWe CANDU nuclear station at its Darlington Nuclear Div. located in Bowmanville. The station operates a Tritium Removal Facility (TRF) to reduce and maintain low tritium levels in the Moderator and Heat Transport heavy water systems of Ontario's CANDU fleet by extracting, concentrating, immobilizing and storing as a metal tritide. Minimizing tritium releases to the environment is of paramount importance to ensure that dose to the public is as low as reasonably achievable (ALARA) and to maintain credibility with the Public. Tritium is removed from the Cryogenic Distillation System to the Tritium Immobilization System (TIS) glove box via a transfer line that is protected by a rupture disc and relief valve. An overpressure event in 2003 had caused the rupture disc to blow, resulting in the release of a significant quantity of elemental tritium into the relief valve discharge line, which ties into the contaminated exhaust system. As a result of a few similar events occurring over a number of years of TRF operation, the released elemental tritium would have been converted to tritium oxide in the presence of a stagnant moist air environment in the stainless steel discharge line. A significant amount of tritium oxide hold-up in the discharge line was anticipated. To minimize any further releases to the environment, a Bubbler System was designed to remove and recover the tritium from the discharge line. This paper summarizes the results of several Bubbler recovery runs that were made over a period of a month. Approximately 3500 Ci of tritium oxide and 230 Ci of elemental tritium were removed and collected. The tritium contained in the water produced from the Bubbler system was later safely recovered in the station's downgraded D{sub 2}O clean-up and recovery system. (authors)

Kalyanam, K.; Leilabadi, A.; El-Behairy, O.; Williams, G. I. D.; Vogt, H. K. [Ontario Power Generation, Darlington Nuclear, PO Box 4000, Bowmanville, ON L1C 3Z8 (Canada)

2008-07-15T23:59:59.000Z

213

Silica Scaling Removal Process  

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

Silica Scaling Removal Process Silica Scaling Removal Process Silica Scaling Removal Process Scientists at Los Alamos National Laboratory have developed a novel technology to remove both dissolved and colloidal silica using small gel particles. Available for thumbnail of Feynman Center (505) 665-9090 Email Silica Scaling Removal Process Applications: Cooling tower systems Water treatment systems Water evaporation systems Potential mining applications (produced water) Industry applications for which silica scaling must be prevented Benefits: Reduces scaling in cooling towers by up to 50% Increases the number of cycles of concentration substantially Reduces the amount of antiscaling chemical additives needed Decreases the amount of makeup water and subsequent discharged water (blowdown) Enables considerable cost savings derived from reductions in

214

Metal Aminoboranes  

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

215

Savannah River Site Removes Dome, Opening Reactor for Recovery Act  

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

Savannah River Site Removes Dome, Opening Reactor for Recovery Act Savannah River Site Removes Dome, Opening Reactor for Recovery Act Decommissioning Savannah River Site Removes Dome, Opening Reactor for Recovery Act Decommissioning American Recovery and Reinvestment Act workers achieved a significant milestone in the decommissioning of a Cold War reactor at the Savannah River Site this month after they safely removed its rusty, orange, 75-foot-tall dome. With the help of a 660-ton crane and lifting lugs, the workers pulled the 174,000-pound dome off the Heavy Water Components Test Reactor, capping more than 16 months of preparations. Savannah River Site Removes Dome, Opening Reactor for Recovery Act Decommissioning More Documents & Publications Recovery Act Changes Hanford Skyline with Explosive Demolitions Recovery Act Workers Add Time Capsule Before Sealing Reactor for Hundreds

216

NETL: Gasification Systems - Warm Gas Multi-Contaminant Removal System  

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

Warm Gas Multi-Contaminant Removal System Warm Gas Multi-Contaminant Removal System Project Number: DE-SC00008243 TDA Research, Inc. is developing a high-capacity, low-cost sorbent that removes anhydrous ammonia (NH3), mercury (Hg), and trace contaminants from coal- and coal/biomass-derived syngas. The clean-up system will be used after the bulk warm gas sulfur removal step, and remove NH3 and Hg in a regenerable manner while irreversibly capturing all other trace metals (e.g., Arsenic, Selenium) reducing their concentrations to sub parts per million (ppm) levels. Current project plans include identifying optimum chemical composition and structure that provide the best sorbent performance for removing trace contaminants, determining the effect of operating parameters, conducting multiple-cycle experiments to test the life of the sorbent for NH3 and Hg removal, and conducting a preliminary design of the sorbent reactor.

217

HEAVY ION INERTIAL FUSION  

E-Print Network (OSTI)

Accelerators as Drivers for Inertially Confined Fusion, W.B.LBL-9332/SLAC-22l (1979) Fusion Driven by Heavy Ion Beams,OF CALIFORNIA f Accelerator & Fusion Research Division

Keefe, D.

2008-01-01T23:59:59.000Z

218

Relativistic Heavy Ion Collider  

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

at the same time. Capable of accelerating 70 trillion protons with every pulse, and heavy ions such as gold and iron, the AGS receives protons and other ions from the AGS...

219

Coated Metal Articles and Method of Making  

DOE Patents (OSTI)

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

Boller, Ernest R.; Eubank, Lowell D.

2004-07-06T23:59:59.000Z

220

STRIPPING METAL COATINGS  

DOE Patents (OSTI)

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

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

1959-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Apparatus and method for removing mercury vapor from a gas stream  

DOE Patents (OSTI)

A metallic filter effectively removes mercury vapor from gas streams. The filter captures the mercury which then can be released and collected as product. The metallic filter is a copper mesh sponge plated with a six micrometer thickness of gold. The filter removes up to 90% of mercury vapor from a mercury contaminated gas stream.

Ganesan, Kumar (Butte, MT)

2008-01-01T23:59:59.000Z

222

Development of an Integrated Multi-Contaminant Removal Process Applied to Warm Syngas Cleanup for Coal-Based Advanced Gasification Systems  

Science Conference Proceedings (OSTI)

This project met the objective to further the development of an integrated multi-contaminant removal process in which H2S, NH3, HCl and heavy metals including Hg, As, Se and Cd present in the coal-derived syngas can be removed to specified levels in a single/integrated process step. The process supports the mission and goals of the Department of Energyâ??s Gasification Technologies Program, namely to enhance the performance of gasification systems, thus enabling U.S. industry to improve the competitiveness of gasification-based processes. The gasification program will reduce equipment costs, improve process environmental performance, and increase process reliability and flexibility. Two sulfur conversion concepts were tested in the laboratory under this project, i.e., the solventbased, high-pressure University of California Sulfur Recovery Process â?? High Pressure (UCSRP-HP) and the catalytic-based, direct oxidation (DO) section of the CrystaSulf-DO process. Each process required a polishing unit to meet the ultra-clean sulfur content goals of <50 ppbv (parts per billion by volume) as may be necessary for fuel cells or chemical production applications. UCSRP-HP was also tested for the removal of trace, non-sulfur contaminants, including ammonia, hydrogen chloride, and heavy metals. A bench-scale unit was commissioned and limited testing was performed with simulated syngas. Aspen-Plus®-based computer simulation models were prepared and the economics of the UCSRP-HP and CrystaSulf-DO processes were evaluated for a nominal 500 MWe, coal-based, IGCC power plant with carbon capture. This report covers the progress on the UCSRP-HP technology development and the CrystaSulf-DO technology.

Howard Meyer

2010-11-30T23:59:59.000Z

223

Heavy fermions in an optical lattice  

Science Conference Proceedings (OSTI)

We employ a mean-field theory to study ground-state properties and transport of a two-dimensional gas of ultracold alkaline-earth-metal atoms governed by the Kondo lattice Hamiltonian plus a parabolic confining potential. In a homogenous system, this mean-field theory is believed to give a qualitatively correct description of heavy-fermion metals and Kondo insulators: It reproduces the Kondo-like scaling of the quasiparticle mass in the former and the same scaling of the excitation gap in the latter. In order to understand ground-state properties in a trap, we extend this mean-field theory via local-density approximation. We find that the Kondo insulator gap manifests as a shell structure in the trapped density profile. In addition, a strong signature of the large Fermi surface expected for heavy-fermion systems survives the confinement and could be probed in time-of-flight experiments. From a full self-consistent diagonalization of the mean-field theory, we are able to study dynamics in the trap. We find that the mass enhancement of quasiparticle excitations in the heavy-Fermi liquid phase manifests as slowing of the dipole oscillations that result from a sudden displacement of the trap center.

Foss-Feig, Michael [Department of Physics, University of Colorado, Boulder, Colorado 80309 (United States); JILA, Boulder, Colorado 80309 (United States); Hermele, Michael; Gurarie, Victor [Department of Physics, University of Colorado, Boulder, Colorado 80309 (United States); Rey, Ana Maria [Department of Physics, University of Colorado, Boulder, Colorado 80309 (United States); JILA, Boulder, Colorado 80309 (United States); National Institute of Standards and Technology, Boulder, Colorado 80309 (United States)

2010-11-15T23:59:59.000Z

224

Experimental Study of In Situ Combustion with Tetralin and Metallic Catalysts.  

E-Print Network (OSTI)

??Experimental studies showed the feasibility of adding metallic catalysts and tetralin for the upgrade and increased recovery of heavy oil during the in situ combustion… (more)

Palmer-Ikuku, Emuobonuvie

2010-01-01T23:59:59.000Z

225

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Towards Heavy Fermions in Europium Intermetallic Compounds Towards Heavy Fermions in Europium Intermetallic Compounds Print Wednesday, 29 July 2009 00:00 For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

226

Accounting strategy of tritium inventory in the heavy water detritiation pilot plant from ICIT Rm. Valcea  

Science Conference Proceedings (OSTI)

In this paper we present a methodology for determination of tritium inventory in a tritium removal facility. The method proposed is based on the developing of computing models for accountancy of the mobile tritium inventory in the separation processes, of the stored tritium and of the trapped tritium inventory in the structure of the process system components. The configuration of the detritiation process is a combination of isotope catalytic exchange between water and hydrogen (LPCE) and the cryogenic distillation of hydrogen isotopes (CD). The computing model for tritium inventory in the LPCE process and the CD process will be developed basing on mass transfer coefficients in catalytic isotope exchange reactions and in dual-phase system (liquid-vapour) of hydrogen isotopes distillation process. Accounting of tritium inventory stored in metallic hydride will be based on in-bed calorimetry. Estimation of the trapped tritium inventory can be made by subtraction of the mobile and stored tritium inventories from the global tritium inventory of the plant area. Determinations of the global tritium inventory of the plant area will be made on a regular basis by measuring any tritium quantity entering or leaving the plant area. This methodology is intended to be applied to the Heavy Water Detritiation Pilot Plant from ICIT Rm. Valcea (Romania) and to the Cernavoda Tritium Removal Facility (which will be built in the next 5-7 years). (authors)

Bidica, N.; Stefanescu, I. [Inst. of Cryogenics and Isotopes Technologies, Uzinei Str. No. 4, Rm. Valcea (Romania); Cristescu, I. [TLK, Forschungszentrum Karlsruhe, Postfach 3640, D76021 Karlsruhe (Germany); Bornea, A.; Zamfirache, M.; Lazar, A.; Vasut, F.; Pearsica, C.; Stefan, I. [Inst. of Cryogenics and Isotopes Technologies, Uzinei Str. No. 4, Rm. Valcea (Romania); Prisecaru, I.; Sindilar, G. [Univ. Politehnica of Bucharest, Splaiul Independentei 313, Bucharest (Romania)

2008-07-15T23:59:59.000Z

227

Method for decontamination of radioactive metal surfaces  

DOE Patents (OSTI)

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

Bray, Lane A. (Richland, WA)

1996-01-01T23:59:59.000Z

228

Ammonia release method for depositing metal oxides  

DOE Patents (OSTI)

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

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

1993-12-31T23:59:59.000Z

229

Method for decontamination of radioactive metal surfaces  

DOE Patents (OSTI)

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

Bray, L.A.

1996-08-13T23:59:59.000Z

230

Super Heavy Element Discovery | ornl.gov  

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

Super Heavy Element Discovery SHARE Super Heavy Element Discovery The location of the Transactinides (super-heavy elements) shown on the Periodic Table. ORNL is internationally...

231

Solenoid transport for heavy ion fusion  

E-Print Network (OSTI)

Transport for Heavy Ion Fusion* Edward Lee** LawrenceHm Heavy Ion Inertial Fusion Abstract Solenoid transport ofseveral stages of a heavy ion fusion driver. In general this

Lee, Edward

2004-01-01T23:59:59.000Z

232

Removable feedwater sparger assembly  

DOE Patents (OSTI)

A removable feedwater sparger assembly includes a sparger having an inlet pipe disposed in flow communication with the outlet end of a supply pipe. A tubular coupling includes an annular band fixedly joined to the sparger inlet pipe and a plurality of fingers extending from the band which are removably joined to a retention flange extending from the supply pipe for maintaining the sparger inlet pipe in flow communication with the supply pipe. The fingers are elastically deflectable for allowing engagement of the sparger inlet pipe with the supply pipe and for disengagement therewith. 8 figs.

Challberg, R.C.

1994-10-04T23:59:59.000Z

233

Heavy ion fusion--Using heavy ions to make electricity  

E-Print Network (OSTI)

in Proc. of the Inertial Fusion Science and ApplicationsP. Abbott, P. F. Peterson, Fusion Science and Technology 44March 15–20, 2004 Heavy Ion Fusion– Using Heavy Ions to Make

Celata, C.M.

2004-01-01T23:59:59.000Z

234

Identifying heavy Higgs bosons  

SciTech Connect

Two techniques for identifying heavy Higgs bosons produced at SSC energies are discussed. In the first, the Higgs boson decays into ZZ, with one Z decaying into an e-pair or ..mu..-pair and the other into a neutrino pair. In the second, the production of the Higgs boson by WW fusion is tagged by detecting the quarks that produced the bremsstrahlung virtual W's. The associated Higgs decay is identified by one leptonic and one hadronic decay. Both methods appear capable of finding a heavy Higgs boson provided the SSC design parameters are achieved. 16 refs., 2 figs., 2 tabs.

Cahn, R.N.

1986-06-01T23:59:59.000Z

235

Advances in Metal Casting Technologies - Molding, Properties and ...  

Science Conference Proceedings (OSTI)

Oct 9, 2012 ... Shot Blasting is a practice commonly used in the metal casting industry to remove sand, small particulates and peen surface. In this experiment ...

236

Astron. Nachr. / AN 335, No. 1, 1 9 (2014) / DOI This.is/not.aDOI High resolution study of the abundance pattern of the heavy elements in  

E-Print Network (OSTI)

of the abundance pattern of the heavy elements in very metal-poor field stars. M. Spite1, and F. Spite1 GEPI, Nucleosynthesis. The abundances of heavy elements in EMP stars are not well explained by the simple view of the r-poor matter. The abundances found in the CEMP- r+s stars reflect the transfer of heavy elements

Recanati, Catherine

237

Nucleic acids encoding metal uptake transporters and their uses  

DOE Patents (OSTI)

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

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

1999-01-01T23:59:59.000Z

238

Removal of fluoride impurities from UF/sub 6/ gas  

DOE Patents (OSTI)

A method of purifying a UF/sub 6/ gas stream containing one or more metal fluoride impurities composed of a transuranic metal, transition metal or mixtures thereof, is carried out by contacting the gas stream with a bed of UF/sub 5/ in a reaction vessel under conditions where at least one impurity reacts with the UF/sub 5/ to form a nongaseous product and a treated gas stream, and removing the treated gas stream from contact with the bed. The nongaseous products are subsequently removed in a reaction with an active fluorine affording agent to form a gaseous impurity which is removed from the reaction vessel. The bed of UF/sub 5/ is formed by the reduction of UF/sub 6/ in the presence of uv light. One embodiment of the reaction vessel includes a plurality of uv light sources as tubes on which UF/sub 5/ is formed. 2 figures.

Beitz, J.V.

1984-01-06T23:59:59.000Z

239

Removal of fluoride impurities from UF.sub.6 gas  

DOE Patents (OSTI)

A method of purifying a UF.sub.6 gas stream containing one or more metal fluoride impurities composed of a transuranic metal, transition metal or mixtures thereof, is carried out by contacting the gas stream with a bed of UF.sub.5 in a reaction vessel under conditions where at least one impurity reacts with the UF.sub.5 to form a nongaseous product and a treated gas stream, and removing the treated gas stream from contact with the bed. The nongaseous products are subsequently removed in a reaction with an active fluorine affording agent to form a gaseous impurity which is removed from the reaction vessel. The bed of UF.sub.5 is formed by the reduction of UF.sub.6 in the presence of UV light. One embodiment of the reaction vessel includes a plurality of UV light sources as tubes on which UF.sub.5 is formed.

Beitz, James V. (Hinsdale, IL)

1985-01-01T23:59:59.000Z

240

A study of plasma etching for use on active metals  

E-Print Network (OSTI)

Active metals can be used as a getter pump, removing impurities in ultra-pure high vacuum environments. To relieve the difficulties involved with the transportation, storage and handling of these metals, a process is being ...

Nishimoto, Keane T. (Keane Takeshi), 1981-

2005-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Methods of removing a constituent from a feed stream using adsorption media  

SciTech Connect

A method of producing an adsorption medium to remove at least one constituent from a feed stream. The method comprises dissolving and/or suspending at least one metal compound in a solvent to form a metal solution, dissolving polyacrylonitrile into the metal solution to form a PAN-metal solution, and depositing the PAN-metal solution into a quenching bath to produce the adsorption medium. The at least one constituent, such as arsenic, selenium, or antimony, is removed from the feed stream by passing the feed stream through the adsorption medium. An adsorption medium having an increased metal loading and increased capacity for arresting the at least one constituent to be removed is also disclosed. The adsorption medium includes a polyacrylonitrile matrix and at least one metal hydroxide incorporated into the polyacrylonitrile matrix.

Tranter, Troy J. (Idaho Falls, ID); Mann, Nicholas R. (Rigby, ID); Todd, Terry A. (Aberdeen, ID); Herbst, Ronald S. (Idaho Falls, ID)

2011-05-24T23:59:59.000Z

242

Heavy Vehicle Systems  

Science Conference Proceedings (OSTI)

Heavy Vehicle (HV) systems are a necessary component of achieving OHVT goals. Elements are in place for a far-ranging program: short, intermediate, and long-term. Solicitation will bring industrial input and support. Future funding trend is positive, outlook for HV systems is good.

Sid Diamond; Richard Wares; Jules Routbort

2000-04-11T23:59:59.000Z

243

Exploiting heavy oil reserves  

E-Print Network (OSTI)

the behaviour of oil and gas prices and the fruits of future exploration. The rate of technological progress. How optimistic are you that the North Sea remains a viable source of oil and gas? A) Our new researchNorth Sea investment potential Exploiting heavy oil reserves Beneath the waves in 3D Aberdeen

Levi, Ran

244

HEAVY WATER COMPONENTS TEST REACTOR DECOMMISSIONING  

Science Conference Proceedings (OSTI)

The Heavy Water Components Test Reactor (HWCTR) Decommissioning Project was initiated in 2009 as a Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) Removal Action with funding from the American Recovery and Reinvestment Act (ARRA). This paper summarizes the history prior to 2009, the major D&D activities, and final end state of the facility at completion of decommissioning in June 2011. The HWCTR facility was built in 1961, operated from 1962 to 1964, and is located in the northwest quadrant of the Savannah River Site (SRS) approximately three miles from the site boundary. The HWCTR was a pressurized heavy water test reactor used to develop candidate fuel designs for heavy water power reactors. In December of 1964, operations were terminated and the facility was placed in a standby condition as a result of the decision by the U.S. Atomic Energy Commission to redirect research and development work on heavy water power reactors to reactors cooled with organic materials. For about one year, site personnel maintained the facility in a standby status, and then retired the reactor in place. In the early 1990s, DOE began planning to decommission HWCTR. Yet, in the face of new budget constraints, DOE deferred dismantlement and placed HWCTR in an extended surveillance and maintenance mode. The doors of the reactor facility were welded shut to protect workers and discourage intruders. In 2009 the $1.6 billion allocation from the ARRA to SRS for site footprint reduction at SRS reopened the doors to HWCTR - this time for final decommissioning. Alternative studies concluded that the most environmentally safe, cost effective option for final decommissioning was to remove the reactor vessel, both steam generators, and all equipment above grade including the dome. The transfer coffin, originally above grade, was to be placed in the cavity vacated by the reactor vessel and the remaining below grade spaces would be grouted. Once all above equipment including the dome was removed, a concrete cover was to be placed over the remaining footprint and the groundwater monitored for an indefinite period to ensure compliance with environmental regulations.

Austin, W.; Brinkley, D.

2011-10-13T23:59:59.000Z

245

HEAVY WATER MODERATED POWER REACTORS. Progress Report for October 1959  

SciTech Connect

Continued progress is reported on the design and construction of the Heavy Water Components Test Reactor; 78% of the firm design and 17% of the construction were complete at the end of October 1959. Approximateiy 15% of the firm design for the isolated coolant loops of the HWCTR was also complete. The results of further fabrication tests and irradiation tests of fuel tubes of natural uranium metal are reported. One of the metal tubes failed under irradiation, while other irradiations of metal fuels progressed satisfactorily. (auth)

Hood, R.R.; Isakoff, L. comps.

1959-11-01T23:59:59.000Z

246

Disposable Absorbent Material for the Removal of Arsenic from Water  

Science Conference Proceedings (OSTI)

Soils and groundwater at many substation sites are contaminated with arsenic-containing compounds. Cost effective water treatment technologies are needed to remove arsenic and other trace metals from underlying aquifers, especially now that drinking water standard for arsenic has been lowered to 10 g/L from the previous value of 50 g/L. The current project tested a disposable ferric oxide adsorbent material, Bayoxide E33, which has been reported to have a high capacity for arsenic removal.

2008-09-10T23:59:59.000Z

247

DEVELOPMENTS IN HEAVY QUARKONIUM SPECTROSCOPY  

E-Print Network (OSTI)

­ 1­ DEVELOPMENTS IN HEAVY QUARKONIUM SPECTROSCOPY Written May 2012 by S. Eidelman (Budker Inst. Navas (Univ. Granada), and C. Patrignani (Univ. Genova, INFN). A golden age for heavy quarkonium physics at HERA and the Tevatron matured; and heavy-ion collisions at RHIC opened a window on the deconfinement

248

Metal Aminoboranes  

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

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

249

Removal of arsenic compounds from petroliferous liquids  

DOE Patents (OSTI)

The present invention in one aspect comprises a process for removing arsenic from petroliferous-derived liquids by contacting said liquid with a divinylbenzene-crosslinked polystyrene polymer (i.e. PS-DVB) having catechol ligands anchored to said polymer, said contacting being at an elevated temperature. In another aspect, the invention is a process for regenerating spent catecholated polystyrene polymer by removal of the arsenic bound to it from contacting petroliferous liquid in accordance with the aspect described above which regenerating process comprises: (a) treating said spent catecholated polystyrene polymer with an aqueous solution of at least one member selected from the group consisting of carbonates and bicarbonates of ammonium, alkali metals, and alkaline earth metals, said solution having a pH between about 8 and 10, and said treating being at a temperature in the range of about 20/sup 0/ to 100/sup 0/C; (b) separating the solids and liquids from each other. In a preferred embodiment the regeneration treatment is in two steps wherein step: (a) is carried out with an aqueous alcoholic carbonate solution which includes at least one lower alkyl alcohol, and, steps (c) and (d) are added. Steps (c) and (d) comprise: (c) treating the solids with an aqueous alcoholic solution of at least one ammonium, alkali or alkaline earth metal bicarbonate at a temperature in the range of about 20 to 100/sup 0/C; and (d) separating the solids from the liquids.

Fish, R.H.

1984-04-06T23:59:59.000Z

250

DOE Removes Brookhaven Contractor  

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

DOE Removes DOE Removes Brookhaven Contractor Peña sends a message to DOE facilities nationwide INSIDE 2 Accelerator Rx 4 FermiKids 6 Spring at Fermilab Photos courtesy of Brookhaven National Laboratory by Judy Jackson, Office of Public Affairs Secretary of Energy Federico Peña announced on Thursday, May 1, that the Department of Energy would immediately terminate the current management contract with Associated Universities, Inc. at Brookhaven National Laboratory in Upton, New York. Peña said that he made the decision after receiving the results of a laboratory safety management review conducted by the independent oversight arm of DOE's Office of Environment, Safety and Health. In addition, the Secretary said he found unacceptable "the continued on page 8 Volume 20 Friday, May 16, 1997

251

Pneumatic soil removal tool  

DOE Patents (OSTI)

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw.

Neuhaus, John E. (Newport News, VA)

1992-01-01T23:59:59.000Z

252

Pneumatic soil removal tool  

Science Conference Proceedings (OSTI)

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw. 3 figs.

Neuhaus, J.E.

1992-10-13T23:59:59.000Z

253

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

254

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

255

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

256

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

257

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

258

Removal of arsenic compounds from petroliferous liquids  

DOE Patents (OSTI)

Described is a process for removing arsenic from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic bound to it from contacting petroliferous liquid as described above and involves: a. treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10 and, b. separating the solids and liquids from each other. Preferably the regeneration treatment is in two steps wherein step (a) is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, steps (a) and (b) are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1985-01-01T23:59:59.000Z

259

Enabling Sustainability through the Physics of Metals & Materials ...  

Science Conference Proceedings (OSTI)

Mar 6, 2013 ... Heavy metals in natural water, industrial water and wastewaters are a worldwide ... complexes is released as HCN gas under strength acidic conditions ... Northern Regions of Russia as Alternative Sources of Pure Water for ...

260

Relativistic Heavy Ion Collider  

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

Relativistic Heavy Ion Collider Relativistic Heavy Ion Collider managed for the U.S. Department of Energy by Brookhaven Science Associates, founded by Stony Brook University and Battelle. managed for the U.S. Department of Energy by Brookhaven Science Associates, a company founded by Stony Brook University and Battelle 07/07 Brookhaven National Laboratory Funded by the U.S. Department of Energy, Brookhaven National Laboratory is a multipurpose research institution located on a 5,300-acre site on Long Island, New York. Six Nobel Prize-winning discoveries have been made at Brookhaven Lab. The Laboratory operates large-scale scientific facilities and performs research in physics, chemistry, biology, medicine, applied science, and

Note: This page contains sample records for the topic "heavy metals removal" 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

Characterizing Heavy Ion  

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

Heavy Ion Heavy Ion Reactions in the 1980's Is there Treasure at the end of the Rainbow? & What happens and how do different modes compete? John Schiffer One of the three research areas for ATLAS, as stated in a 1984 document to Congress: Are there some new marvelous symmetries, hidden in resonances in heavier nuclei, beyond 12 C+ 12 C and its immediate vicinity? (s.c. linac work, pre-ATLAS) Other attempts to chase the rainbow 180 o elastic scattering of 12 C on 40 Ca shows structure Fusion of 16 O on 40 Ca does not. In the end, it seemed that these structures were sometimes present in alpha-particle nuclei, but almost never in others. Some optimists, continued the pursuit. We also looked at the total fusion cross section in systems that showed resonances in scattering.

262

Computing Heavy Elements  

E-Print Network (OSTI)

Reliable calculations of the structure of heavy elements are crucial to address fundamental science questions such as the origin of the elements in the universe. Applications relevant for energy production, medicine, or national security also rely on theoretical predictions of basic properties of atomic nuclei. Heavy elements are best described within the nuclear density functional theory (DFT) and its various extensions. While relatively mature, DFT has never been implemented in its full power, as it relies on a very large number (~ 10^9-10^12) of expensive calculations (~ day). The advent of leadership-class computers, as well as dedicated large-scale collaborative efforts such as the SciDAC 2 UNEDF project, have dramatically changed the field. This article gives an overview of the various computational challenges related to the nuclear DFT, as well as some of the recent achievements.

Schunck, N; Kortelainen, M; McDonnell, J; Moré, J; Nazarewicz, W; Pei, J; Sarich, J; Sheikh, J; Staszczak, A; Stoitsov, M; Wild, S M

2011-01-01T23:59:59.000Z

263

Computing Heavy Elements  

E-Print Network (OSTI)

Reliable calculations of the structure of heavy elements are crucial to address fundamental science questions such as the origin of the elements in the universe. Applications relevant for energy production, medicine, or national security also rely on theoretical predictions of basic properties of atomic nuclei. Heavy elements are best described within the nuclear density functional theory (DFT) and its various extensions. While relatively mature, DFT has never been implemented in its full power, as it relies on a very large number (~ 10^9-10^12) of expensive calculations (~ day). The advent of leadership-class computers, as well as dedicated large-scale collaborative efforts such as the SciDAC 2 UNEDF project, have dramatically changed the field. This article gives an overview of the various computational challenges related to the nuclear DFT, as well as some of the recent achievements.

N. Schunck; A. Baran; M. Kortelainen; J. McDonnell; J. Moré; W. Nazarewicz; J. Pei; J. Sarich; J. Sheikh; A. Staszczak; M. Stoitsov; S. M. Wild

2011-07-25T23:59:59.000Z

264

Heavy Vehicle Propulsion Materials  

DOE Green Energy (OSTI)

The objectives are to Provide Key Enabling Materials Technologies to Increase Energy Efficiency and Reduce Exhaust Emissions. The following goals are listed: Goal 1: By 3rd quarter 2002, complete development of materials enabling the maintenance or improvement of fuel efficiency {ge} 45% of class 7-8 truck engines while meeting the EPA/Justice Department ''Consent Decree'' for emissions reduction. Goal 2: By 4th quarter 2004, complete development of enabling materials for light-duty (class 1-2) diesel truck engines with efficiency over 40%, over a wide range of loads and speeds, while meeting EPA Tier 2 emission regulations. Goal 3: By 4th quarter 2006, complete development of materials solutions to enable heavy-duty diesel engine efficiency of 50% while meeting the emission reduction goals identified in the EPA proposed rule for heavy-duty highway engines.''

Ray Johnson

2000-01-31T23:59:59.000Z

265

Heavy Ions - Cyclotron  

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

Heavy Ions Heavy Ions Heavy ions used at the BASE Facility are accelerated in the form of "cocktails," named because of the fact that several heavy ions with the same mass-to-charge ratio are sent into the Cyclotron, which accelerates the ions while acting as a precision mass separator. The Control Room Operator then uses Cyclotron frequency to select only the desired ion, a process that takes about 2 minutes. We provide four standard cocktails: 4.5, 10, 16, and 30 MeV/nucleon. Depending on the cocktail, LETs from 1 to 100 MeV/(mg/cm^2) and flux levels of up to 1E7 ions/cm2-sec are available. Parts are tested in our vacuum chamber, and can be remotely positioned horizontally, vertically, or rotationally (y and z axes) with the motion table. An alignment laser is available to ensure the part is in the center of the beam. Mounting hardware is readily available. 12xBNC (F-F), 2x25-pin D (F-M or M-F), 4x40-pin flat ribbon (M-M), 4x50-pin flat ribbon (M-M), 12xSMA (F-F), and 2xEthernet vacuum feedthroughs are mounted upon request. (The 4x40-pin and 4x50-pin flat ribbon connectors are wired straight across, so you will need a F-F adapter to correct the pin numbers to normal.) Holes are provided through the cave shielding blocks for connecting additional test equipment, with a distance of approximately 10 feet from vacuum feedthrough to the top of the shielding block.

266

Utah Heavy Oil Program  

Science Conference Proceedings (OSTI)

The Utah Heavy Oil Program (UHOP) was established in June 2006 to provide multidisciplinary research support to federal and state constituents for addressing the wide-ranging issues surrounding the creation of an industry for unconventional oil production in the United States. Additionally, UHOP was to serve as an on-going source of unbiased information to the nation surrounding technical, economic, legal and environmental aspects of developing heavy oil, oil sands, and oil shale resources. UHOP fulGilled its role by completing three tasks. First, in response to the Energy Policy Act of 2005 Section 369(p), UHOP published an update report to the 1987 technical and economic assessment of domestic heavy oil resources that was prepared by the Interstate Oil and Gas Compact Commission. The UHOP report, entitled 'A Technical, Economic, and Legal Assessment of North American Heavy Oil, Oil Sands, and Oil Shale Resources' was published in electronic and hard copy form in October 2007. Second, UHOP developed of a comprehensive, publicly accessible online repository of unconventional oil resources in North America based on the DSpace software platform. An interactive map was also developed as a source of geospatial information and as a means to interact with the repository from a geospatial setting. All documents uploaded to the repository are fully searchable by author, title, and keywords. Third, UHOP sponsored Give research projects related to unconventional fuels development. Two projects looked at issues associated with oil shale production, including oil shale pyrolysis kinetics, resource heterogeneity, and reservoir simulation. One project evaluated in situ production from Utah oil sands. Another project focused on water availability and produced water treatments. The last project considered commercial oil shale leasing from a policy, environmental, and economic perspective.

J. Bauman; S. Burian; M. Deo; E. Eddings; R. Gani; R. Goel; C.K. Huang; M. Hogue; R. Keiter; L. Li; J. Ruple; T. Ring; P. Rose; M. Skliar; P.J. Smith; J.P. Spinti; P. Tiwari; J. Wilkey; K. Uchitel

2009-10-20T23:59:59.000Z

267

Interim Report on Uranium Metal Segregation Testing  

SciTech Connect

This report describes the preliminary results of laboratory and bench-scale vendor testing to evaluate the effectiveness of the gravity mineral concentration technology for removing and concentrating uranium metal from K Basin sludge.

Schmidt, Andrew J.; Elmore, Monte R.

2004-04-18T23:59:59.000Z

268

Workers Demolish Metals Plant at Paducah Site | Department of Energy  

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

Demolish Metals Plant at Paducah Site Demolish Metals Plant at Paducah Site Workers Demolish Metals Plant at Paducah Site February 21, 2013 - 12:00pm Addthis The Metals Plant is shown before workers removed panels from the structure ln 2012. The Metals Plant is shown before workers removed panels from the structure ln 2012. Workers remove panels from the Metals Plant in September 2012. Workers remove panels from the Metals Plant in September 2012. About half of the complex was demolished by the end of December 2012, ahead of schedule. About half of the complex was demolished by the end of December 2012, ahead of schedule. An ultra-high-reach demolition machine — similar to equipment used to demolish Yankee Stadium — cuts into upper portions of the building’s last standing section late last month.

269

METHOD OF CLEANING METAL SURFACES  

DOE Patents (OSTI)

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

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

1959-05-19T23:59:59.000Z

270

Method for removal of explosives from aqueous solution using suspended plant cells  

DOE Patents (OSTI)

The use of plant suspension cultures to remove ionic metallic species and TNT-based explosives and their oxidation products from aqueous solution is described. Several plant strains were investigated including D. innoxia, Citrus citrus, and Black Mexican Sweet Corn. All showed significant ability to remove metal ions. Ions removed to sub-ppm levels include barium, iron, and plutonium. D. innoxia cells growing in media containing weapons effluent contaminated with Ba.sup.2+ also remove TNT, other explosives and oxidation products thereof from solution. The use of dead, dehydrated cells was also found to be of use in treating waste directly.

Jackson, Paul J. (Los Alamos, NM); Torres, deceased, Agapito P. (late of Los Alamos, NM); Delhaize, Emmanuel (Giralang, AU)

1994-01-01T23:59:59.000Z

271

Phytoremediation of Metal-Contaminated Soils  

DOE Green Energy (OSTI)

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

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

2004-03-31T23:59:59.000Z

272

Cooling and solidification of heavy hydrocarbon liquid streams  

DOE Patents (OSTI)

A process and apparatus for cooling and solidifying a stream of heavy hydrocarbon material normally boiling above about 850.degree. F., such as vacuum bottoms material from a coal liquefaction process. The hydrocarbon stream is dropped into a liquid bath, preferably water, which contains a screw conveyor device and the stream is rapidly cooled, solidified and broken therein to form discrete elongated particles. The solid extrudates or prills are then dried separately to remove substantially all surface moisture, and passed to further usage.

Antieri, Salvatore J. (Trenton, NJ); Comolli, Alfred G. (Yardley, PA)

1983-01-01T23:59:59.000Z

273

Engine Removal Projection Tool  

DOE Green Energy (OSTI)

The US Navy has over 3500 gas turbine engines used throughout the surface fleet for propulsion and the generation of electrical power. Past data is used to forecast the number of engine removals for the next ten years and determine engine down times between removals. Currently this is done via a FORTRAN program created in the early 1970s. This paper presents results of R&D associated with creating a new algorithm and software program. We tested over 60 techniques on data spanning 20 years from over 3100 engines and 120 ships. Investigated techniques for the forecast basis including moving averages, empirical negative binomial, generalized linear models, Cox regression, and Kaplan Meier survival curves, most of which are documented in engineering, medical and scientific research literature. We applied those techniques to the data, and chose the best algorithm based on its performance on real-world data. The software uses the best algorithm in combination with user-friendly interfaces and intuitively understandable displays. The user can select a specific engine type, forecast time period, and op-tempo. Graphical displays and numerical tables present forecasts and uncertainty intervals. The technology developed for the project is applicable to other logistic forecasting challenges.

Ferryman, Thomas A.; Matzke, Brett D.; Wilson, John E.; Sharp, Julia L.; Greitzer, Frank L.

2005-06-02T23:59:59.000Z

274

High-resolution lithography based on selective removal of atoms  

Science Conference Proceedings (OSTI)

A new method of high-resolution lithography based on selective removal of atoms is described. Drawbacks of lift-off lithography in comparison with the method proposed are pointed out and test structures of metal (Mo) stripes with a thickness of 50 nm are obtained.

Domantovskii, A. G.; Gurovich, B. A.; Maslakov, K. I. [Russian Research Centre Kurchatov Institute (Russian Federation)

2006-12-15T23:59:59.000Z

275

Process for removal of sulfur oxides from waste gases  

Science Conference Proceedings (OSTI)

A process for removing sulfur oxides from waste gas is provided. The gas is contacted with a sorbent selected from sodium bicarbonate, trona and activated sodium carbonate and, utilizing an alkaline liquor containing borate ion so as to reduce flow rates and loss of alkalinity, the spent sorbent is regenerated with an alkaline earth metal oxide or hydroxide.

Lowell, P.S.; Phillips, J.L.

1983-05-24T23:59:59.000Z

276

Slag capture and removal during laser cutting. [Patent application  

DOE Patents (OSTI)

Molten metal removed from a workpiece in a laser cutting operation is blown away from the cutting point by a gas jet and collected on an electromagnet. The laser cutting is used to separate the castings of spent fuel rods from the fuel-containing elements therein.

Brown, C.O.

1982-01-28T23:59:59.000Z

277

Securing the metal recycling chain for the steel industry by detecting orphan radioactive sources in scrap metal  

SciTech Connect

Experimental tests are reported for the detection of the heavy metal shielding of orphan sources hidden inside scrap metal by using a recently developed muon tomography system. Shielded sources do not trigger alarm in radiation portal commonly employed at the entrance of steel industry using scrap metal. Future systems integrating radiation portals with muon tomography inspection gates will substantially reduce the possibility of accidental melting of radioactive sources securing the use of recycled metal.

Pesente, S.; Benettoni, M.; Checchia, P.; Conti, E.; Gonella, F.; Nebbia, G. [INFN Sezione di Padova, via Marzolo 8, 35131 Padova Italy (Italy); Vanini, S.; Viesti, G.; Zumerle, G. [INFN Sezione di Padova, via Marzolo 8, 35131 Padova Italy (Italy); University of Padova and INFN Sezione di Padova, via Marzolo 8, 35131 Padova Italy (Italy); Bonomi, G.; Zenoni, A. [University of Brescia, via Branze 38, 25123 Brescia and INFN Sezione di Pavia, via Bassi 6, 27100 Pavia (Italy); Calvini, P.; Squarcia, S. [University of Genova and INFN Sezione di Genova, via Dodecaneso 33, 16146 Genova (Italy)

2010-08-04T23:59:59.000Z

278

Gel bead composition for metal adsorption  

DOE Patents (OSTI)

The invention is a gel bead comprising propylene glycol alginate and bone gelatin and is capable of removing metals such as Sr and Cs from solution without adding other adsorbents. The invention could have application to the nuclear industry's waste removal activities.

Scott, Charles D. (Oak Ridge, TN); Woodward, Charlene A. (Oak Ridge, TN); Byers, Charles H. (Oak Ridge, TN)

1991-01-01T23:59:59.000Z

279

Gel bead composition for metal adsorption  

DOE Patents (OSTI)

The invention is a gel bead comprising propylene glycol alginate and bone gelatin and is capable of removing metals such as Sr and Cs from solution without adding other adsorbents. The invention could have application to the nuclear industry's waste removal activities.

Scott, Charles D. (Oak Ridge, TN); Woodward, Charlene A. (Oak Ridge, TN); Byers, Charles H. (Oak Ridge, TN)

1990-01-01T23:59:59.000Z

280

Gel bead composition for metal adsorption  

DOE Patents (OSTI)

The invention is a gel bead comprising propylene glycol alginate and bone gelatin and is capable of removing metals such as Sr and Cs from solution without adding other adsorbents. The invention could have application to the nuclear industry's waste removal activities. 4 tabs.

Scott, C.D.; Woodward, C.A.; Byers, C.H.

1989-04-04T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Coordination chemistry of two heavy metals: I, Ligand preferences in lead(II) complexation, toward the development of therapeutic agents for lead poisoning: II, Plutonium solubility and speciation relevant to the environment  

SciTech Connect

The coordination chemistry and solution behavior of the toxic ions lead(II) and plutonium(IV, V, VI) have been investigated. The ligand pK{sub a}s and ligand-lead(II) stability constants of one hydroxamic acid and four thiohydroaxamic acids were determined. Solution thermodynamic results indicate that thiohydroxamic acids are more acidic and slightly better lead chelators than hydroxamates, e.g., N-methylthioaceto-hydroxamic acid, pK{sub a} = 5.94, log{beta}{sub 120} = 10.92; acetohydroxamic acid, pK{sub a} = 9.34, log{beta}{sub l20} = 9.52. The syntheses of lead complexes of two bulky hydroxamate ligands are presented. The X-ray crystal structures show the lead hydroxamates are di-bridged dimers with irregular five-coordinate geometry about the metal atom and a stereochemically active lone pair of electrons. Molecular orbital calculations of a lead hydroxamate and a highly symmetric pseudo octahedral lead complex were performed. The thermodynamic stability of plutonium(IV) complexes of the siderophore, desferrioxamine B (DFO), and two octadentate derivatives of DFO were investigated using competition spectrophotometric titrations. The stability constant measured for the plutonium(IV) complex of DFO-methylterephthalamide is log{beta}{sub 110} = 41.7. The solubility limited speciation of {sup 242}Pu as a function of time in near neutral carbonate solution was measured. Individual solutions of plutonium in a single oxidation state were added to individual solutions at pH = 6.0, T = 30.0, 1.93 mM dissolved carbonate, and sampled over intervals up to 150 days. Plutonium solubility was measured, and speciation was investigated using laser photoacoustic spectroscopy and chemical methods.

Neu, M.P. [Lawrence Berkeley Lab., CA (United States)

1993-11-01T23:59:59.000Z

282

Heavy Truck Engine Program  

DOE Green Energy (OSTI)

The Heavy Duty Truck Engine Program at Cummins embodied three significant development phases. All phases of work strove to demonstrate a high level of diesel engine efficiency in the face of increasingly stringent emission requirements. Concurrently, aftertreatment system development and refinement was pursued in support of these efficiency demonstrations. The program's first phase focused on the demonstration in-vehicle of a high level of heavy duty diesel engine efficiency (45% Brake Thermal Efficiency) at a typical cruise condition while achieving composite emissions results which met the 2004 U.S. EPA legislated standards. With a combination of engine combustion calibration tuning and the development and application of Urea-based SCR and particulate aftertreatment, these demonstrations were successfully performed by Q4 of 2002. The second phase of the program directed efforts towards an in-vehicle demonstration of an engine system capable of meeting 2007 U.S. EPA legislated emissions requirements while achieving 45% Brake Thermal Efficiency at cruise conditions. Through further combustion optimization, the refinement of Cummins Cooled EGR architecture, the application of a high pressure common rail fuel system and the incorporation of optimized engine parasitics, Cummins Inc. successfully demonstrated these deliverables in Q2 of 2004. The program's final phase set a stretch goal of demonstrating 50% Brake Thermal Efficiency from a heavy duty diesel engine system capable of meeting 2010 U.S. EPA legislated emissions requirements. Cummins chose to pursue this goal through further combustion development and refinement of the Cooled EGR system architecture and also applied a Rankine cycle Waste Heat Recovery technique to convert otherwise wasted thermal energy to useful power. The engine and heat recovery system was demonstrated to achieve 50% Brake Thermal Efficiency while operating at a torque peak condition in second quarter, 2006. The 50% efficient engine system was capable of meeting 2010 emissions requirements through the application of NOx and particulate matter reduction techniques proven earlier in the program.

Nelson, Christopher

2009-01-08T23:59:59.000Z

283

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

Office of Scientific and Technical Information (OSTI)

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

284

Technology Analysis - Heavy Vehicle Technologies  

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

the GPRA benefits estimates for EERE's Vehicle Technologies Program's heavy vehicle technology research activities. Argonne researchers develop the benefits analysis using four...

285

DEDICATED HEAVY ION MEDICAL ACCELERATORS  

E-Print Network (OSTI)

et al. , ,8iolog·ical and Medical Research with Acceleratedet al. , "Biological and Medical Research with J\\cceleratedic Heavy Ions in Medical and Scientific Research, Edmonton,

Gough, R.A.

2013-01-01T23:59:59.000Z

286

Heavy Ion Fusion development plan  

SciTech Connect

Some general cnsiderations in the fusion development program are given. The various factors are considered that must be determined before heavy ion fusion can be assessed. (MOW)

Maschke, A.W.

1978-01-01T23:59:59.000Z

287

Air toxics from heavy oil production and consumption  

SciTech Connect

This report assesses the potential impact of recent Federal and state regulations for airborne toxic substances on the production and consumption of heavy fuel oils. Emissions of nickel from heavy oil production in California are considered in some detail, in conjunction with California state regulations for toxic emissions. Although the use of thermal energy from heavy crude oils could in theory be impacted by toxic air pollution regulations, recent trends towards the use of natural gas for the required extraction energy appear to provide substantial relief, in addition to reducing emissions of criteria air pollutants. However, the consumption of residual fuel oils containing toxic metals could result in higher population exposures to these substances and their attendant risks may be worthy of more detailed analysis.

Lipfert, F.W.; DePhillips, M.P.; Moskowitz, P.D.

1992-12-22T23:59:59.000Z

288

The Role of the Flexicoking Process in Heavy Oil Processing  

E-Print Network (OSTI)

The recently commercialized FLEXICOKING Process has a significant role to play in developing, known heavy oil reserves. The process upgrades virtually any pumpable feed including residual, pitch or total crude. Combined with HYDROFINING, it produces a clean product slate composed of low Btu gas, high Btu gas, LPG, naphtha, distillate and gas oil. The low Btu gas falls within the definition of an "Alternate Fuel" under current legislation (PL 95-620). Originally developed for refinery bottoms conversion, the FLEXICOKING process can also be used as the primary technology for Stand Alone Energy Centers upgrading low quality, high metals, heavy crudes. These efficient energy centers can be located either at a heavy oil production field or integrated with an energy-intensive industrial complex.

Taylor, R. I.

1980-01-01T23:59:59.000Z

289

Geothermal hydrogen sulfide removal  

DOE Green Energy (OSTI)

UOP Sulfox technology successfully removed 500 ppM hydrogen sulfide from simulated mixed phase geothermal waters. The Sulfox process involves air oxidation of hydrogen sulfide using a fixed catalyst bed. The catalyst activity remained stable throughout the life of the program. The product stream composition was selected by controlling pH; low pH favored elemental sulfur, while high pH favored water soluble sulfate and thiosulfate. Operation with liquid water present assured full catalytic activity. Dissolved salts reduced catalyst activity somewhat. Application of Sulfox technology to geothermal waters resulted in a straightforward process. There were no requirements for auxiliary processes such as a chemical plant. Application of the process to various types of geothermal waters is discussed and plans for a field test pilot plant and a schedule for commercialization are outlined.

Urban, P.

1981-04-01T23:59:59.000Z

290

Pneumatic soil removal tool  

Science Conference Proceedings (OSTI)

A soil tool is provided for removing radioactive soil, rock and debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator value mounted on the handle, to provide movement of the movable jaw.

Neuhaus, J.F.

1991-01-23T23:59:59.000Z

291

Very high energy heavy-ion accelerators  

SciTech Connect

A review is given of various programs for building heavy ion accelerators. Topics discussed are (1) options of reaching very high energies with heavy ions; (2) present performance of the superHILAC and the Bevalac; (3) heavy ion sources; (4) applications of heavy ion accelerators outside of basic research; and (5) reliability and operating costs of heavy ion sources. (PMA)

Grunder, H.A.

1975-10-01T23:59:59.000Z

292

Heavy Vehicle Propulsion Materials: Recent Progress and Future Plans  

DOE Green Energy (OSTI)

The Heavy Vehicle Propulsion Materials Program provides enabling materials technology for the U.S. DOE Office of Heavy Vehicle Technologies (OHVT). The technical agenda for the program is based on an industry assessment and the technology roadmap for the OHVT. A five-year program plan was published in 2000. Major efforts in the program are materials for diesel engine fuel systems, exhaust aftertreatment, and air handling. Additional efforts include diesel engine valve-train materials, structural components, and thermal management. Advanced materials, including high-temperature metal alloys, intermetallics, cermets, ceramics, amorphous materials, metal- and ceramic-matrix composites, and coatings, are investigated for critical engine applications. Selected technical issues and planned and ongoing projects as well as brief summaries of several technical highlights are given.

D. Ray Johnson; Sidney Diamond

2001-05-14T23:59:59.000Z

293

Heavy Machine Shop | Central Fabrication Services | Brookhaven...  

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

Heavy Machine Shop Heavy Machine Shop The Heavy Machine Shop facility is located in building 479, and may be accessed by the main door on the north face or front of the building....

294

Liquid metal cooled nuclear reactor plant system  

DOE Patents (OSTI)

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

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

1993-01-01T23:59:59.000Z

295

Analysis of heavy oils: Method development and application to Cerro Negro heavy petroleum  

Science Conference Proceedings (OSTI)

On March 6, 1980, the US Department of Energy (DOE) and the Ministry of Energy and Mines of Venezuela (MEMV) entered into a joint agreement which included analysis of heavy crude oils from the Venezuelan Orinoco oil belt.The purpose of this report is to present compositional data and describe new analytical methods obtained from work on the Cerro Negro Orinoco belt crude oil since 1980. Most of the chapters focus on the methods rather than the resulting data on Cerro Negro oil, and results from other oils obtained during the verification of the method are included. In addition, published work on analysis of heavy oils, tar sand bitumens, and like materials is reviewed, and the overall state of the art in analytical methodology for heavy fossil liquids is assessed. The various phases of the work included: distillation and determination of routine'' physical/chemical properties (Chapter 1); preliminary separation of >200{degree}C distillates and the residue into acid, base, neutral, saturated hydrocarbon and neutral-aromatic concentrates (Chapter 2); further separation of acid, base, and neutral concentrates into subtypes (Chapters 3-5); and determination of the distribution of metal-containing compounds in all fractions (Chapter 6).

Carbognani, L.; Hazos, M.; Sanchez, V. (INTEVEP, Filial de Petroleos de Venezuela, SA, Caracas (Venezuela)); Green, J.A.; Green, J.B.; Grigsby, R.D.; Pearson, C.D.; Reynolds, J.W.; Shay, J.Y.; Sturm, G.P. Jr.; Thomson, J.S.; Vogh, J.W.; Vrana, R.P.; Yu, S.K.T.; Diehl, B.H.; Grizzle, P.L.; Hirsch, D.E; Hornung, K.W.; Tang, S.Y.

1989-12-01T23:59:59.000Z

296

PROCESS FOR TREATING VOLATILE METAL FLUORIDES  

DOE Patents (OSTI)

This patent relates to the purification of uranium hexafluoride, made by reacting the metal or its tetrafluoride with fluorine, from the frequently contained traces of hydrofluoric acid. According to the present process, UF/sub 6/ containing as an impurity a small amount of hydrofluoric acid, is treated to remove such impurity by contact with an anhydrous alkali metal fluoride such as sodium fluoride. In this way a non-volatile complex containing hydrofluoric acid and the alkali metal fluoride is formed, and the volatile UF /sub 6/ may then be removed by distillation.

Rudge, A.J.; Lowe, A.J.

1957-10-01T23:59:59.000Z

297

9 Treatment of Metal-Bearing Effluents: Removal and  

E-Print Network (OSTI)

conveyed by means of gravity water jets or centrifugal umps. Lift Maximum safe vertical distance hrough the operation of contactors and auxiliary de vices of an electric system. Natural gas A gaseous fuel occurring

Volesky, Bohumil

298

CAST SHOP TECHNOLOGY: VII: Metal Treatment--Inclusion Removal  

Science Conference Proceedings (OSTI)

This paper presents the morphological aspects of the major inclusions commonly seen in AA3104 can stock alloy. The potential sources which may introduce ...

299

Removal of Xenon and Krypton from Air Using Metal Organic ...  

Science Conference Proceedings (OSTI)

... two gases is cryogenic distillation which is an energy-intensive process. ... Determining Thermal Conductivity of Simulated Feed for High Level Waste Glass.

300

Heavy crude oil recovery  

SciTech Connect

The oil crisis of the past decade has focused most of the attention and effort of researchers on crude oil resources, which are accepted as unrecoverable using known technology. World reserves are estimated to be 600-1000 billion metric tons, and with present technology 160 billion tons of this total can be recovered. This book is devoted to the discussion of Enhanced Oil Recovery (EOR) techniques, their mechanism and applicability to heavy oil reservoirs. The book also discusses some field results. The use of numerical simulators has become important, in addition to laboratory research, in analysing the applicability of oil recovery processes, and for this reason the last section of the book is devoted to simulators used in EOR research.

Okandan, E.

1984-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

HEAVY ION LINEAR ACCELERATOR  

DOE Patents (OSTI)

A linear accelerator of heavy ions is described. The basic contributions of the invention consist of a method and apparatus for obtaining high energy particles of an element with an increased charge-to-mass ratio. The method comprises the steps of ionizing the atoms of an element, accelerating the resultant ions to an energy substantially equal to one Mev per nucleon, stripping orbital electrons from the accelerated ions by passing the ions through a curtain of elemental vapor disposed transversely of the path of the ions to provide a second charge-to-mass ratio, and finally accelerating the resultant stripped ions to a final energy of at least ten Mev per nucleon.

Van Atta, C.M.; Beringer, R.; Smith, L.

1959-01-01T23:59:59.000Z

302

Removal to Maximum Extent Practical  

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

Summary Notes from 1 November 2007 Generic Technical Issue Discussion on Removal of Highly Radioactive Radionuclides/Key Radionuclides to the Maximum Extent Practical

303

Light Metals  

Science Conference Proceedings (OSTI)

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

304

Organoclay Sorbent for Removal of Carbon Dioxide from Gas Streams at Low Temperatures  

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

Organoclay Sorbent for Removal of Carbon Dioxide from Gas Organoclay Sorbent for Removal of Carbon Dioxide from Gas Streams at Low Temperatures Contact NETL Technology Transfer Group techtransfer@netl.doe.gov October 2012 Significance * Energy mixing is maximized * Mobilizing of the particulates is complete * No "dead zones" exist * Packing of material is minimized * Eroding effects are significantly reduced Applications * Mixing nuclear waste at Hanford * Any similar industrial process involving heavy solids in a carrier fluid Opportunity Research is currently active on the patent-pending technology "Organoclay Sorbent for Removal of Carbon Dioxide from

305

SYNCHROTRONS FOR HEAVY IONS - BEVALAC EXPERIENCE  

E-Print Network (OSTI)

Heavy Ions ir. Medical and Scientific Research", Edmonton,Heavy Ions in Medical and Scientific Research" Edmonton,vigorous medical and nuclear science research groups. The

Grunder, H.A.

2010-01-01T23:59:59.000Z

306

Glimpse of heavy electrons reveals "hidden order"  

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

Glimpse of heavy electrons reveals "hidden order" Glimpse of heavy electrons reveals "hidden order" The remarkable breakthrough helps validate theory behind the observed increase...

307

Method for improved decomposition of metal nitrate solutions  

DOE Patents (OSTI)

A method for co-conversion of aqueous solutions of one or more heavy metal nitrates is described, wherein thermal decomposition within a temperature range of about 300 to 800/sup 0/C is carried out in the presence of about 50 to 500% molar concentration of ammonium nitrate to total metal.

Haas, P.A.; Stines, W.B.

1981-01-21T23:59:59.000Z

308

Method for improved decomposition of metal nitrate solutions  

DOE Patents (OSTI)

A method for co-conversion of aqueous solutions of one or more heavy metal nitrates wherein thermal decomposition within a temperature range of about 300.degree. to 800.degree. C. is carried out in the presence of about 50 to 500% molar concentration of ammonium nitrate to total metal.

Haas, Paul A. (Knoxville, TN); Stines, William B. (Knoxville, TN)

1983-10-11T23:59:59.000Z

309

Heavy ion fusion--Using heavy ions to make electricity  

E-Print Network (OSTI)

for a practical fusion power reactor. HIF is the only fusionenter the reactor chamber, and focus Heavy Ion Fusion ontoengineering test reactor. The promise of fusion as a power

Celata, C.M.

2004-01-01T23:59:59.000Z

310

Heavy Ion Collisions at RHIC  

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

at Heavy Ion Colliders at Heavy Ion Colliders Theory Drivers & View from LHC Urs Achim Wiedemann CERN PH-TH NSAC Implementation Subcommittee Hearings 7 September 2012 Heavy Ion Physics - Main Tools of Theorists Understanding properties of hot and dense matter from the elementary interactions in QCD High Energy Physics String Theory Computational Physics Fluid Dynamics Dissipative fluid dynamic description * Based on: E-p conservation: 2 nd law of thermodynamics: * Sensitive to properties of matter that are calculated from first principles in quantum field theory - EOS: and sound velocity - transport coefficients: shear , bulk viscosity, conductivities ...

311

Metal decontamination for waste minimization using liquid metal refining technology  

Science Conference Proceedings (OSTI)

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

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

1993-09-01T23:59:59.000Z

312

3M heavy duty roto peen: Baseline report; Greenbook (chapter)  

SciTech Connect

The heavy-duty roto peen technology is being evaluated at Florida International University (FIU) as a baseline technology. It is a commercially available technology and has been used for various projects at locations throughout the country. In conjunction with FIU`s evaluation of efficiency and cost, this report covers the human factors assessment for safety and health issues. The heavy-duty roto peen allows for the selective removal of concrete substrates. The peen is a tungsten carbide shot brazed to a hardened steel rivet that is supported by a heavy-duty flexible flap. The shot rivet is kept captive to the tool by mounting the roto peen in a slotted hub. The heavy-duty roto peen is designed to be used with several commercially available pieces of equipment. The equipment being used will determine the width of each pass. The equipment being used with the roto peen is then connected to a vacuum system for dust collection during scabbling. The safety and health evaluation during the human factors assessment focused on two main areas: noise and dust.

NONE

1997-07-31T23:59:59.000Z

313

3M heavy duty roto peen: Baseline report  

SciTech Connect

The heavy-duty roto peen technology was being evaluated at Florida International University (FIU) as a baseline technology. It is a commercially available technology and has been used for various projects at locations throughout the country. In conjunction with FIU`s evaluation of efficiency and cost, this report covers the human factors assessment for safety and health issues. The heavy-duty roto peen allows for the selective removal of concrete substrates. The peen is a tungsten carbide shot brazed to a hardened steel rivet that is supported by a heavy-duty flexible flap. The shot rivet is kept captive to the tool by mounting the roto peen in a slotted hub. The heavy-duty roto peen is designed to be used with several commercially available pieces of equipment. The equipment being used will determine the width of each pass. The equipment being used with the roto peen is then connected to a vacuum system for dust collection during scabbling. The safety and health evaluation during the human factors assessment focused on two main areas: noise and dust.

NONE

1997-07-31T23:59:59.000Z

314

RHIC | Relativistic Heavy Ion Collider  

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

Relativistic Heavy Ion Collider Relativistic Heavy Ion Collider Photo of LINAC The Relativistic Heavy Ion Collider (RHIC) is a world-class particle accelerator at Brookhaven National Laboratory where physicists are exploring the most fundamental forces and properties of matter and the early universe. RHIC accelerates beams of particles (e.g., the nuclei of heavy atoms such as gold) to nearly the speed of light, and smashes them together to recreate a state of matter thought to have existed immediately after the Big Bang some 13.8 billion years ago. STAR and PHENIX, two large detectors located around the 2.4-mile-circumference accelerator, take "snapshots" of these collisions to reveal a glimpse of the basic constituents of visible matter, quarks and gluons. Understanding matter at

315

The physics of heavy flavors  

SciTech Connect

We review the physics of heavy quark flavors, including weak decays, onium, tau leptons, mixing, the Kobayashi-Maskawa matrix, and CP violation in B decay. 36 refs., 12 figs.

Gilman, F.J.

1987-12-01T23:59:59.000Z

316

RHIC | Relativistic Heavy Ion Collider  

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

indicate that collisions of small particles with large gold nuclei at the Relativistic Heavy Ion Collider may be serving up miniscule servings of hot quark-gluon plasma. RHIC...

317

Relativistic Heavy Ion Collider, RHIC  

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

The Relativistic Heavy Ion Collider website has moved to www.bnl.govrhicdefault.asp Sponsored by the U.S. Department of Energy Office of Science, Office of Nuclear Physics. Last...

318

Fuel cell with metal screen flow-field - Energy Innovation Portal  

Building Energy Efficiency ... Solar Thermal; ... and a metal mesh flow field therebetween for distributing cooling water flow over the electrodes to remove heat ...

319

CRBRP decay heat removal systems  

SciTech Connect

The Decay Heat Removal Systems for the Clinch River Breeder Reactor Plant (CRBRP) are designed to adequately remove sensible and decay heat from the reactor following normal shutdown, operational occurrences, and postulated accidents on both a short term and a long term basis. The Decay Heat Removal Systems are composed of the Main Heat Transport System, the Main Condenser and Feedwater System, the Steam Generator Auxiliary Heat Removal System (SGAHRS), and the Direct Heat Removal Service (DHRS). The overall design of the CRBRP Decay Heat Removal Systems and the operation under normal and off-normal conditions is examined. The redundancies of the system design, such as the four decay heat removal paths, the emergency diesel power supplies, and the auxiliary feedwater pumps, and the diversities of the design such as forced circulation/natural circulation and AC Power/DC Power are presented. In addition to overall design and system capabilities, the detailed designs for the Protected Air Cooled Condensers (PACC) and the Air Blast Heat Exchangers (ABHX) are presented.

Hottel, R.E.; Louison, R.; Boardman, C.E.; Kiley, M.J.

1977-01-01T23:59:59.000Z

320

LCLS Heavy Met Outgassing Tests  

Science Conference Proceedings (OSTI)

A Heavy Met that is 95% tungsten, 3% nickel and 2% iron and sintered to 100% density and is Ultra High Vacuum (UHV) compatible is proposed for use as the X-ray slit in the Front End Enclosure and the Fixed Mask for the Linac Coherent Light Source (LCLS). The Heavy Met was tested in the LLNL Vacuum Sciences and Engineering Lab (VSEL) to determine its outgassing rate and its overall compatibility with the vacuum requirements for LCLS.

Kishiyama, K. I.

2010-12-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Preliminary Heavy Metal Survey of a Spent Alkaline Battery Waste ...  

Science Conference Proceedings (OSTI)

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

322

United abominations: Density functional studies of heavy metal chemistry  

Science Conference Proceedings (OSTI)

Carbonyl and nitrile addition to uranyl (UO{sup 2}{sup 2+}) are studied. The competition between nitrile and water ligands in the formation of uranyl complexes is investigated. The possibility of hypercoordinated uranyl with acetone ligands is examined. Uranyl is studied with diactone alcohol ligands as a means to explain the apparent hypercoordinated uranyl. A discussion of the formation of mesityl oxide ligands is also included. A joint theory/experimental study of reactions of zwitterionic boratoiridium(I) complexes with oxazoline-based scorpionate ligands is reported. A computational study was done of the catalytic hydroamination/cyclization of aminoalkenes with zirconium-based catalysts. Techniques are surveyed for programming for graphical processing units (GPUs) using Fortran.

Schoendorff, George

2012-04-02T23:59:59.000Z

323

Biosorption of Heavy Metal Ions from Wastewater by ... - TMS  

Science Conference Proceedings (OSTI)

Aug 1, 2003 ... TMS Member price: 10.00. Non-member price: 25.00. TMS Student Member price : 10.00. Product In Stock. Description The ability of ...

324

Method and device for electroextraction of heavy metals from ...  

The main advantage of the invention is the improvement in rate of ... Applications and Industries. ... Six cylindrical steel electrodes form two triode ...

325

Theoretical Studies on Heavy Metal Sulfides in Solution  

DOE Green Energy (OSTI)

'Calculating the stabilities, Raman and UV spectra and acidities of As sulfides in aqueous solution', J. A. Tossell, M. D. Zimmermann and G. R. Helz. Some of the Raman spectra obtained by reacting aqueous As(OH)3 with aqueous bisulfide are shown, taken from Wood, et al. (2002). To interpret these spectra we have carried out an extensive series of calculations, detailed for the case of AsS(SH){sub 2}{sup -} in Table 1 below. By employing state of the art quantum chemical techniques to determine gas-phase harmonic and anharmonic frequencies and solution phase corrections we can accurately match features in the experimental spectrum shown in the top figure. The AsS(SH){sub 2}{sup -}...22 H{sub 2}O nanocluster employed is shown in the lower figure. For this species we have calculated the equilibrium structure and the harmonic vibrational spectrum at the CBSB7 B3LYP level. For the free solute species AsS(SH){sub 2}{sup -} we have carried out a whole series of calculations, evaluating harmonic and anharmonic vibrational frequencies at a number of different quantum mechanical levels. In the spectra below, Fig. 3 and Fig. 5 from Wood, et al. (2002), the features around 700-800 cm{sup -1} are attributed to As-O stretches and those around 350-450 cm{sup -1} to As-S stretches. In the nanocluster an isolated vibrational feature is observed at 425 cm{sup -1}, an As=S stretch, close to the value (415 cm{sup -1}) determined by Wood, et al. (2002). Analysis of the calculated frequencies for AsS(SH){sub 2}{sup -} within a polarizable continuum model yields a similar result. Taking the highest level harmonic results, obtained from a CCSD calculation, and adding anharmonic and PCM corrections at the B3LYP level (designated (3) + (5) - (1) in Table 1) gives a frequency for the intense high frequency As=S stretch within 15 cm{sup -1} of experiment. Although there is still interesting work to be done on the stabilities and the Raman and UV spectra of As sulfides, most of the basic concepts have been worked out and we are therefore proposing to move to a new area, that of humic acids (while continuing our studies complexes formed by As oxides and sulfides, now applied to functional groups present in humic acids).

Tossell, John A.

2007-10-31T23:59:59.000Z

326

Phosphate and thermal stabilization of heavy metals in dredged sediments.  

E-Print Network (OSTI)

??Treatment and reuse of dredged harbor sediments in construction as an alternative to disposal reduces costs and conserves resources. This research focused on leachability of… (more)

Ndiba, Peter Kuria

2009-01-01T23:59:59.000Z

327

Modeling the Removal of Uranium U(VI) from Aqueous Solutions in the  

E-Print Network (OSTI)

, the amount of radioactive heavy metal waste sludge or brine generated has the potential to be significant of the mixed cell culture in a chemostat was carried out on an insulated magnetic stirrer inananaerobicchamber into a 15 mL conical tube, and anaerobically sealed (90% N2, 5% CO2, and 5% H2). The tubes were shipped

328

Precious Metals  

Science Conference Proceedings (OSTI)

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

329

Article removal device for glovebox  

DOE Patents (OSTI)

An article removal device for a glovebox is described comprising a conduit extending through a glovebox wall which may be closed by a plug within the glovebox, and a fire-resistant container closing the outer end of the conduit and housing a removable container for receiving pyrophoric or otherwise hazardous material without disturbing the interior environment of the glovebox or adversely affecting the environment outside of the glovebox. (Official Gazette)

Guyer, R.H.; Leebl, R.G.

1973-12-01T23:59:59.000Z

330

Heavy vehicle propulsion system materials program semiannual progress report for April 1999 through September 1999  

DOE Green Energy (OSTI)

The purpose of the Heavy Vehicle Propulsion System Materials Program is the development of materials: ceramics, intermetallics, metal alloys, and metal and ceramic coatings, to support the dieselization of class 1-3 trucks to realize a 35% fuel-economy improvement over current gasoline-fueled trucks and to support commercialization of fuel-flexible LE-55 low-emissions, high-efficiency diesel engines for class 7-8 trucks.

Johnson, D.R.

2000-01-01T23:59:59.000Z

331

Tritium removal from contaminated water via infrared laser multiple-photon dissociation  

Science Conference Proceedings (OSTI)

Isotope separation by means of infrared-laser multiple-photon dissociation offers an efficient way to recover tritium from contaminated light or heavy water found in fission and fusion reactors. For tritium recovery from heavy water, chemical exchange of tritium into deuterated chloroform is followed by selective laser dissociation of tritiated chloroform and removal of the tritiated photoproduct, TCl. The single-step separation factor is at least 2700 and is probably greater than 5000. Here we present a description of the tritium recovery process, along with recent accomplishments in photochemical studies and engineering analysis of a recovery system.

Maienschein, J.L.; Magnotta, F.; Herman, I.P.; Aldridge, F.T.; Hsiao, P.

1983-01-01T23:59:59.000Z

332

Enhanced heat transfer with metal wool filled tubes  

SciTech Connect

The Advanced Photon Source (APS) to be constructed at Argonne National Laboratory (ANL) utilizes magnetic devices which generate x-ray beams with very intense heat flux levels. The flux levels encountered can be one or two orders of magnitude higher than those commonly found in nuclear reactors or fusion devices. The beam line elements and optics on such beams pose significant challenge to the researchers and designers to keep them cooled at acceptable levels of surface temperature and/or temperature gradients. Therefore, methods and techniques achieving heat removal enhancement are constantly sought. One such technique suggested and considered is the use of conductive metal wool filled tubes where the filter is brazed to the tube walls. A comparative investigation of the conventionally achievable heat transfer coefficient h'' with water and the wall conductance of a heavy wall copper tube reveals that major resistance is on the coolant side. Therefore, there exists a significant opportunity to improve heat transfer in the tubes by enhancement of the coolant side. To this end a variety of copper wool filled tubes as well as a commercially available enhanced copper tube were subjected to laboratory tests with water and conventional heating to assess the resulting heat transfer improvement. Design improvements using enhanced cooling are discussed in terms of structural weight, controls, grazing angles, the operational reliability. 9 refs., 11 figs., 5 tabs.

Kuzay, T.M.; Collins, J.T.; Khounsary, A.M. (Argonne National Lab., IL (USA)); Morales, G. (Argonne National Lab., IL (USA) Texas Univ., El Paso, TX (USA))

1990-08-01T23:59:59.000Z

333

Waste removal in pyrochemical fuel processing for the Integral Fast Reactor  

SciTech Connect

Electrorefining in a molten salt electrolyte is used in the Integral Fast Reactor fuel cycle to recover actinides from spent fuel. Processes that are being developed for removing the waste constituents from the electrorefiner and incorporating them into the waste forms are described in this paper. During processing, halogen, chalcogen, alkali, alkaline earth, and rare earth fission products build up in the molten salt as metal halides and anions, and fuel cladding hulls and noble metal fission products remain as metals of various particle sizes. Essentially all transuranic actinides are collected as metals on cathodes, and are converted to new metal fuel. After processing, fission products and other waste are removed to a metal and a mineral waste form. The metal waste form contains the cladding hulls, noble metal fission products, and (optionally) most rare earths in a copper or stainless steel matrix. The mineral waste form contains fission products that have been removed from the salt into a zeolite or zeolite-derived matrix.

Ackerman, J.P.; Johnson, T.R.; Laidler, J.J.

1994-01-01T23:59:59.000Z

334

Heavy oil reservoirs recoverable by thermal technology. Annual report  

SciTech Connect

This volume contains reservoir, production, and project data for target reservoirs which contain heavy oil in the 8 to 25/sup 0/ API gravity range and are susceptible to recovery by in situ combustion and steam drive. The reservoirs for steam recovery are less than 2500 feet deep to comply with state-of-the-art technology. In cases where one reservoir would be a target for in situ combustion or steam drive, that reservoir is reported in both sections. Data were collectd from three source types: hands-on (A), once-removed (B), and twice-removed (C). In all cases, data were sought depicting and characterizing individual reservoirs as opposed to data covering an entire field with more than one producing interval or reservoir. The data sources are listed at the end of each case. This volume also contains a complete listing of operators and projects, as well as a bibliography of source material.

Kujawa, P.

1981-02-01T23:59:59.000Z

335

High removal rate laser-based coating removal system  

DOE Patents (OSTI)

A compact laser system that removes surface coatings (such as paint, dirt, etc.) at a removal rate as high as 1000 ft.sup.2 /hr or more without damaging the surface. A high repetition rate laser with multiple amplification passes propagating through at least one optical amplifier is used, along with a delivery system consisting of a telescoping and articulating tube which also contains an evacuation system for simultaneously sweeping up the debris produced in the process. The amplified beam can be converted to an output beam by passively switching the polarization of at least one amplified beam. The system also has a personal safety system which protects against accidental exposures.

Matthews, Dennis L. (Moss Beach, CA); Celliers, Peter M. (Berkeley, CA); Hackel, Lloyd (Livermore, CA); Da Silva, Luiz B. (Danville, CA); Dane, C. Brent (Livermore, CA); Mrowka, Stanley (Richmond, CA)

1999-11-16T23:59:59.000Z

336

A full featured monitoring, control and data management system for liquid metal coolant loops  

Science Conference Proceedings (OSTI)

The heavy liquid metals (HLM) lead and lead-bismuth are considered as coolant and spallation material in accelerator driven systems (ADS) for nuclear waste transmutation. To investigate the viability of HLM cooled reactor systems the Karlsruhe Lead Laboratory ...

Cord H. Lefhalm; Viktor Krieger

2005-06-01T23:59:59.000Z

337

Reductive dissolution and metal transport in lake coeur d alene sediments  

E-Print Network (OSTI)

in Coeur d'Alene Lake, Idaho. Environ. Sci. Technol. 32,heavy metals in the sediment of Lake Coeur d'Alene, Idaho.Masters Thesis, University of Idaho, Moscow, Idaho. Zachara,

Sengor, Sevinc.S.; Spycher, Nicolas.F.; Ginn, Timothy.R.; Moberly, James; Peyton, B.; Sani, Rajesh.K.

2007-01-01T23:59:59.000Z

338

Carbonized material adsorbents for the removal of mercury from aqueous solutions  

SciTech Connect

Although wood has essentially been excluded as a starting material for the production of granular activated carbon because of the poor strength and friability of the products, powdered wood based activated carbons are still being used in water treatment and other liquid phase applications. However, the capability of powdered wood-based charcoal which in itself porous has not been fully known. Few studies have been conducted in harnessing its potential for adsorption purposes especially in water treatment. This study was conducted to investigate the possibility of using wood based carbonized materials from Sugi (Cryptomeria japonica D. Don) as adsorption materials in aqueous solutions of heavy metals like mercury, zinc, lead, cadmium and arsenic. However, of all the heavy metals investigated, mercury is considered to be the most toxic so this paper describes only the adsorption ability of the carbonized materials in adsorbing this metal from aqueous solutions of different concentrations.

Ishihara, S.; Pulido, L.L. [Kyoto Univ. (Japan); Kajimoto, T. [Wakayama Industrial Technology Center (Japan)

1996-12-31T23:59:59.000Z

339

Removal - An alternative to clearance  

SciTech Connect

This presentation shows the differences between the application of clearance and removal, both being procedures for materials leaving radiation protection areas permanently. The differentiation will be done on the basis of the German legislation but may be also applicable for other national legislation. For clearance in Germany two basic requirements must be given, i.e. that the materials are activated or contaminated and that they result from the licensed use or can be assigned to the scope of the license. Clearance needs not to be applied to objects in Germany which are to be removed only temporarily from controlled areas with the purpose of repair or reuse in other controlled areas. In these cases only the requirements of contamination control apply. In the case of removal it must either be proved by measurements that the relevant materials are neither activated nor contaminated or that the materials result from areas where activation or contamination is impossible due to the operational history considering operational procedures and events. If the material is considered neither activated nor contaminated there is no need for a clearance procedure. Therefore, these materials can be removed from radiation protection areas and the removal is in the responsibility of the licensee. Nevertheless, the removal procedure and the measuring techniques to be applied for the different types of materials need an agreement from the competent authority. In Germany a maximum value of 10% of the clearance values has been established in different licenses as a criterion for the application of removal. As approximately 2/3 of the total mass of a nuclear power plant is not expected to be contaminated or activated there is a need for such a procedure of removal for this non contaminated material without any regulatory control especially in the case of decommissioning. A remarkable example is NPP Stade where in the last three years more than 8600 Mg were disposed of by removal and only 315 Mg were released by clearance, even before the decommissioning licensing procedure was finished. (authors)

Feinhals, J.; Kelch, A. [TUV NORD SysTec GmbH and Co. KG, Hamburg (Germany); Kunze, V. [Federal Office for Radiation Protection, Salzgitter (Germany)

2007-07-01T23:59:59.000Z

340

RHIC | Relativistic Heavy Ion Collider  

NLE Websites -- All DOE Office Websites

Brookhaven National Laboratory Brookhaven National Laboratory search U.S. Department of Energy logo Home RHIC Science News Images Videos For Scientists Björn Schenke 490th Brookhaven Lecture, 12/18 Join Björn Schenke of Brookhaven Lab's Physics Department for the 490th Brookhaven Lecture, titled 'The Shape and Flow of Heavy Ion Collisions,' on Wednesday, Dec. 18, at 4 p.m. in Berkner Hall. droplets Tiny Drops of Hot Quark Soup-How Small Can They Be? New analyses indicate that collisions of small particles with large gold nuclei at the Relativistic Heavy Ion Collider may be serving up miniscule servings of hot quark-gluon plasma. RHIC Physics RHIC is the first machine in the world capable of colliding ions as heavy as gold. The Spin Puzzle RHIC is the world's only machine capable of colliding beams of polarized

Note: This page contains sample records for the topic "heavy metals removal" 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

CMVRTC: Heavy Truck Duty Cycle  

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

heavy truck duty cycle (HTDC) project heavy truck duty cycle (HTDC) project OVERVIEW The Heavy Truck Duty Cycle (HTDC) Project was initiated in 2004 and is sponsored by the US Department of Energy's (DOE's) Office of FreedomCar and Vehicle Technologies Program. ORNL designed the research program to generate real-world-based duty cycle data from trucks operating in long-haul operations and was designed to be conducted in three phases: identification of parameters to be collected, instrumentation and pilot testing, identification of a real-world fleet, design of the data collection suite and fleet instrumentation, and data collection, analysis, and development of a duty cycle generation tool (DCGT). ANL logo dana logo michelin logo Schrader logo This type of data will be useful for supporting energy efficiency

342

Jet quenching and heavy quarks  

E-Print Network (OSTI)

Jet quenching and more generally physics at high transverse momentum P_T scales is a cornerstone of the heavy-ion physics program at the LHC. In this work, the current understanding of jet quenching in terms of a QCD shower evolution being modified by the surrounding medium is reviewed along with the evidence for this picture from light parton high P_T observables. Conceptually, the same QCD shower description should also be relevant for heavy quarks, but with several important modifications introduced by the quark masses. Thus especially in the limit of small jet energy over quark mass E_jet/m_q, the relevant physics may be rather different from light quark jets, and several attempts to explain the observed phenomenology of heavy quarks at high P_T are discussed here.

Thorsten Renk

2013-09-12T23:59:59.000Z

343

Large Component Removal/Disposal  

Science Conference Proceedings (OSTI)

This paper describes the removal and disposal of the large components from Maine Yankee Atomic Power Plant. The large components discussed include the three steam generators, pressurizer, and reactor pressure vessel. Two separate Exemption Requests, which included radiological characterizations, shielding evaluations, structural evaluations and transportation plans, were prepared and issued to the DOT for approval to ship these components; the first was for the three steam generators and one pressurizer, the second was for the reactor pressure vessel. Both Exemption Requests were submitted to the DOT in November 1999. The DOT approved the Exemption Requests in May and July of 2000, respectively. The steam generators and pressurizer have been removed from Maine Yankee and shipped to the processing facility. They were removed from Maine Yankee's Containment Building, loaded onto specially designed skid assemblies, transported onto two separate barges, tied down to the barges, th en shipped 2750 miles to Memphis, Tennessee for processing. The Reactor Pressure Vessel Removal Project is currently under way and scheduled to be completed by Fall of 2002. The planning, preparation and removal of these large components has required extensive efforts in planning and implementation on the part of all parties involved.

Wheeler, D. M.

2002-02-27T23:59:59.000Z

344

Vietnam HEU Removal | National Nuclear Security Administration  

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

Removal NNSANews posted a photo: Vietnam HEU Removal A truck carrying the last highly enriched uranium in Vietnam winds through the Vietnamese countryside. Facebook Twitter Youtube...

345

Accelerators for heavy ion fusion  

SciTech Connect

Large fusion devices will almost certainly produce net energy. However, a successful commercial fusion energy system must also satisfy important engineering and economic constraints. Inertial confinement fusion power plants driven by multi-stage, heavy-ion accelerators appear capable of meeting these constraints. The reasons behind this promising outlook for heavy-ion fusion are given in this report. This report is based on the transcript of a talk presented at the Symposium on Lasers and Particle Beams for Fusion and Strategic Defense at the University of Rochester on April 17-19, 1985.

Bangerter, R.O.

1985-10-01T23:59:59.000Z

346

Actinide removal from spent salts  

DOE Patents (OSTI)

A method for removing actinide contaminants (uranium and thorium) from the spent salt of a molten salt oxidation (MSO) reactor is described. Spent salt is removed from the reactor and analyzed to determine the contaminants present and the carbonate concentration. The salt is dissolved in water, and one or more reagents are added to precipitate the thorium as thorium oxide and/or the uranium as either uranium oxide or as a diuranate salt. The precipitated materials are filtered, dried and packaged for disposal as radioactive waste. About 90% of the thorium and/or uranium present is removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be dried and returned to the reactor for re-use. Salt solutions containing a carbonate concentration <20% require further clean-up using an ion exchange column, which yields salt solutions that contain less than 0.1 ppm of thorium or uranium.

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

2002-01-01T23:59:59.000Z

347

Work plan, AP-102 mixer pump removal and pump replacement  

DOE Green Energy (OSTI)

The objective of this work plan is to plan the steps and estimate the costs required to remove the failed AP-102 mixer pump, and to plan and estimate the cost of the necessary design and specification work required to order a new, but modified, mixer pump including the pump and pump pit energy absorbing design. The main hardware required for the removal of the mixer is as follows: a flexible receiver and blast shield; a metal container for the pulled mixer pump; and a trailer and strongback to haul and manipulate the container. Additionally: a gamma scanning device will be needed to detect the radioactivity emanating from the mixer as it is pulled from the tank; a water spray system will be required to remove tank waste from the surface of the mixer as it is pulled from the AP-102 tank; and a lifting yoke to lift the mixer from the pump pit (the SY-101 Mixer Lifting Yoke will be used). A ``green house`` will have to be erected over the AP-102 pump pit and an experienced Hoisting and Rigging crew must be assembled and trained in mixer pump removal methods before the actual removal is undertaken.

Jimenez, R.F.

1994-09-01T23:59:59.000Z

348

Recovery Act Funds Test Reactor Dome Removal in Historic D&D Project |  

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

Recovery Act Funds Test Reactor Dome Removal in Historic D&D Recovery Act Funds Test Reactor Dome Removal in Historic D&D Project Recovery Act Funds Test Reactor Dome Removal in Historic D&D Project February 1, 2011 - 12:00pm Addthis Media Contacts Jim Giusti, DOE (803) 952-7697 james-r.giusti@srs.gov Paivi Nettamo, SRNS (803) 646-6075 paivi.nettamo@srs.gov AIKEN, S.C. - The landscape of the Savannah River Site (SRS) is a little flatter and a little less colorful with the removal today of the 75-foot-tall rusty-orange dome from the Cold War-era test reactor. This $25-million reactor decommissioning and deactivation project is funded By the American Recovery and Reinvestment Act. Affectionately known by SRS employees as "Hector," the iconic Heavy Water Components Test Reactor (HWCTR) has stood in the Site's B Area since 1959

349

Process for converting heavy oil deposited on coal to distillable oil in a low severity process  

DOE Patents (OSTI)

A process for removing oil from coal fines that have been agglomerated or blended with heavy oil comprises the steps of heating the coal fines to temperatures over 350.degree. C. up to 450.degree. C. in an inert atmosphere, such as steam or nitrogen, to convert some of the heavy oil to lighter, and distilling and collecting the lighter oils. The pressure at which the process is carried out can be from atmospheric to 100 atmospheres. A hydrogen donor can be added to the oil prior to deposition on the coal surface to increase the yield of distillable oil.

Ignasiak, Teresa (417 Heffernan Drive, Edmonton, Alberta, CA); Strausz, Otto (13119 Grand View Drive, Edmonton, Alberta, CA); Ignasiak, Boleslaw (417 heffernan Drive, Edmonton, Alberta, CA); Janiak, Jerzy (17820 - 76 Ave., Edmonton, Alberta, CA); Pawlak, Wanda (3046 - 11465 - 41 Avenue, Edmonton, Alberta, CA); Szymocha, Kazimierz (3125 - 109 Street, Edmonton, Alberta, CA); Turak, Ali A. (Edmonton, CA)

1994-01-01T23:59:59.000Z

350

Hadron Production in Heavy Ion Collisions  

E-Print Network (OSTI)

2A GeV 3 Hadron Production from AGS to RHIC 3.1 SystematicsHadron Production in Heavy Ion Collisions Hans Georg RitterAC02- 05CH11231. Hadron Production in Heavy Ion Collisions

Ritter, Hans Georg

2009-01-01T23:59:59.000Z

351

Heavy Vehicle and Engine Resource Guide  

DOE Green Energy (OSTI)

The Heavy Vehicle and Engine Resource Guide is a catalog of medium- and heavy-duty engines and vehicles with alternative fuel and advanced powertrain options. This edition covers model year 2003 engines and vehicles.

Not Available

2004-03-01T23:59:59.000Z

352

Proton Distribution in Heavy Nuclei  

DOE R&D Accomplishments (OSTI)

It is reasoned that, from considerations connected with beta-decay stability and Coulomb repulsion forces, a neutron excess is developed on the surface of heavy nuclei. Several consequences of this qualitative analysis in nucleon interactions are briefly noted. (K.S.)

Johnson, M. H; Teller, E.

1953-11-13T23:59:59.000Z

353

Summary of the Heavy Flavours Working Group  

E-Print Network (OSTI)

This is a summary of the contributions presented in the Heavy Flavours Working Group of the DIS2006 Workshop.

U. Karshon; I. Schienbein; P. Thompson

2006-08-10T23:59:59.000Z

354

Light-Heavy Price Difference Varies  

U.S. Energy Information Administration (EIA)

Light-Heavy Price Difference Varies ; Function of Crude Market Factors ; Function of Conversion Capacity ; Function of Product Market Factors

355

Oklahoma Refinery Catalytic Hydrotreating, Heavy Gas Oil ...  

U.S. Energy Information Administration (EIA)

Cat. Hydro. Heavy Gas Oil Downstream Charge Capacity (B/SD)y ; Oklahoma Downstream Charge Capacity of Operable Petroleum Refineries ...

356

Heavy Vehicle and Engine Resource Guide  

DOE Green Energy (OSTI)

A comprehensive product catalog of medium and heavy-duty engines and vehicles with alternative fuel and advanced powertrain options.

Not Available

2001-10-01T23:59:59.000Z

357

Mississippi Refinery Catalytic Hydrotreating, Heavy Gas Oil ...  

U.S. Energy Information Administration (EIA)

Cat. Hydro. Heavy Gas Oil Downstream Charge Capacity (B/SD)y ; Mississippi Downstream Charge Capacity of Operable Petroleum Refineries ...

358

Liquid metal cooled nuclear reactors with passive cooling system  

SciTech Connect

A liquid metal cooled nuclear reactor having a passive cooling system for removing residual heat resulting from fuel decay during reactor shutdown. The passive cooling system comprises a plurality of cooling medium flow circuits which cooperate to remove and carry heat away from the fuel core upon loss of the normal cooling flow circuit to areas external thereto.

Hunsbedt, Anstein (Los Gatos, CA); Fanning, Alan W. (San Jose, CA)

1991-01-01T23:59:59.000Z

359

Demonstrate the removal efficiency and capacity of MOF materials for krypton recovery  

Science Conference Proceedings (OSTI)

Metal organic framework materials (MOFs) were developed and tested in support of the U.S. Department of Energy Office of Nuclear Energy, Fuel Cycle Technology Separations and Waste Forms Campaign. Specifically, materials are being developed for the removal of xenon (Xe) and krypton (Kr) from gaseous products of nuclear fuel reprocessing unit operations. Two metal organic framework structures were investigated in greater detail to demonstrate the removal efficiency and capacity of MOF materials for krypton recovery. Our two bed breakthrough measurements on NiDOBDC and FMOFCu indicate these materials can capture and separate parts per million levels of Xe and Kr from air. The removal efficiency and adsorption capacity for Kr on these two MOFs were further increased upon removal of Xe upfront.

Thallapally, Praveen K.; Liu, Jian; Strachan, Denis M.

2013-08-23T23:59:59.000Z

360

Forecast Technical Document Felling and Removals  

E-Print Network (OSTI)

Forecast Technical Document Felling and Removals Forecasts A document describing how volume fellings and removals are handled in the 2011 Production Forecast system. Tom Jenkins Robert Matthews Ewan Mackie Lesley Halsall #12;PF2011 ­ Felling and removals forecasts Background A fellings and removals

Note: This page contains sample records for the topic "heavy metals removal" 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

Heavy Tails: Performance Models and Scheduling Disciplines  

E-Print Network (OSTI)

Heavy Tails: Performance Models and Scheduling Disciplines Sindo N´u~nez-Queija based on joint ITC´u~nez-Queija CWI & TU/e #12;Heavy Tails: Performance Models and Scheduling Disciplines Part I ­ Introduction and Methodology Tales to tell: · traffic measurements and statistical analysis · traffic modeling · heavy

Núñez-Queija, Rudesindo

362

Finding Interesting Correlations with Conditional Heavy Hitters  

E-Print Network (OSTI)

Finding Interesting Correlations with Conditional Heavy Hitters Katsiaryna Mirylenka, Themis Srivastava AT&T Labs, Florham Park, NJ, USA {graham, divesh}@research.att.com Abstract-- The notion of heavy of Conditional Heavy Hitters to identify such items, with applications in network monitoring, and Markov chain

Palpanas, Themis

363

Isolation of Metals from Liquid Wastes: Reactive in Turbulent Thermal Reactors  

SciTech Connect

A Generic Technology for treatment of DOE Metal-Bearing Liquid Waste The DOE metal-bearing liquid waste inventory is large and diverse, both with respect to the metals (heavy metals, transuranics, radionuclides) themselves, and the nature of the other species (annions, organics, etc.) present. Separation and concentration of metals is of interest from the standpoint of reducing the volume of waste that will require special treatment or isolation, as well as, potentially, from the standpoint of returning some materials to commerce by recycling. The variety of metal-bearing liquid waste in the DOE complex is so great that it is unlikely that any one process (or class of processes) will be suitable for all material. However, processes capable of dealing with a wide variety of wastes will have major advantages in terms of process development, capital, and operating costs, as well as in environmental and safety permitting. Moreover, to the extent that a process operates well with a variety of metal-bearing liquid feedwastes, its performance is likely to be relatively robust with respect to the inevitable composition variations in each waste feed. One such class of processes involves high-temperature treatment of atomized liquid waste to promote reactive capture of volatile metallic species on collectible particulate substrates injected downstream of a flame zone. Compared to low-temperature processes that remove metals from the original liquid phase by extraction, precipitation, ion exchange, etc., some of the attractive features of high-temperature reactive scavenging are: The organic constituents of some metal-bearing liquid wastes (in particular, some low-level mixed wastes) must be treated thermally in order to meet the requirements of the Resource Conservation and Recovery Act (RCRA) and Toxic Substances Control Act (TSCA), and the laws of various states. No species need be added to an already complex liquid system. This is especially important in light of the fact that DOE has already experienced problems with organic complexants added to precipitate radionuclides. For example, the Defense Nuclear Facilities Safety Board has expressed, in a formal Recommendation to the Secretary of Energy, its concern about the evolution of benzene vapor in concentrations greater then the lower flammability limit from tanks to which sodium tetraphenylborate has been added to precipitate 137Cs in the ''In-Tank Precipitation'' (ITP) process at the Savannah River Site. Other species added to the waste in the ITP process are sodium titanate (to adsorb 90Sr and Pu), and oxalic acid. Avoiding addition of organics to radioactive waste has the additional advantage that is likely to significantly reduce the rate of radiolytic and radiolytically-induced hydrogen generation (c.f. Meisel et al., [1993]), in which it is shown that removal of organics reduces the rate of hydrogen generation in simulated waste from Hanford tank 241-SY-101 by over 70%. Organic species already present are destroyed with very high efficiency. This attribute is especially attractive with respect to high-level tank waste at the Hanford Site, in which large amounts of citrate, glyoxylate, EDTA (ethylenediaminetetraacetic acid), and HEDTA [N-(2- hydroxyethyl)-ethylenediaminetriacetic acid] were added to precipitate radionuclides. These organic species are important in the thermal and radiolytic generation of methane, hydrogen, and nitrous oxide, flammable mixtures of which are episodically vented from 25 tanks on Hanford's Flammable Gas Watch List [Hopkins, 1994]. The same basic approach can be used to treat a broad range of liquid wastes, in each case concentrating the metals (regardless of liquid-phase oxidation state or association with chelators or absorbents) using a collectible sorbent, and destroying any organic species present. In common with the Army's approach (see section 2.2) to the thermal destruction of a 10 range of chemical warfare agents (GB, VX, and two blister agents), this may drastically simplify process and plant design and

Wendt, Jost O.L.

2001-09-30T23:59:59.000Z

364

High removal rate laser-based coating removal system  

Science Conference Proceedings (OSTI)

A compact laser system is disclosed that removes surface coatings (such as paint, dirt, etc.) at a removal rate as high as 1,000 ft{sup 2}/hr or more without damaging the surface. A high repetition rate laser with multiple amplification passes propagating through at least one optical amplifier is used, along with a delivery system consisting of a telescoping and articulating tube which also contains an evacuation system for simultaneously sweeping up the debris produced in the process. The amplified beam can be converted to an output beam by passively switching the polarization of at least one amplified beam. The system also has a personal safety system which protects against accidental exposures.

Matthews, D.L.; Celliers, P.M.; Hackel, L.; Da Silva, L.B.; Dane, C.B.; Mrowka, S.

1999-11-16T23:59:59.000Z

365

HEAVY BARYONS: A COMBINED LARGE Nc AND HEAVY QUARK EXPANSION FOR ELECTROWEAK CURRENTS  

E-Print Network (OSTI)

The combined large Nc and heavy quark limit for baryons containing a single heavy quark is discussed. The combined large Nc and heavy quark expansion of the heavy quark bilinear operators is obtained. In the combined expansion the corrections proportional to mN/mQ are summed to all orders. In particular, the combined expansion can be used to determine semileptonic form factors of heavy baryons in the combined limit. 1

Boris A. Gelman

2002-01-01T23:59:59.000Z

366

Bounds on Heavy-to-Heavy Weak Decay Form Factors  

E-Print Network (OSTI)

We provide upper and lower bounds on the semileptonic weak decay form factors for $B \\to D^(*)$ and $\\Lambda_b \\to \\Lambda_c$ decays by utilizing inclusive heavy quark effective theory sum rules. These bounds are calculated to second order in $\\Lambda_{QCD}/m_Q$ and first order in $\\alpha_s$. The $O(\\alpha_s^2 \\beta_0)$ corrections to the bounds at zero recoil are also presented.

Chiang, C W

2001-01-01T23:59:59.000Z

367

Bounds on Heavy-to-Heavy Weak Decay Form Factors  

E-Print Network (OSTI)

We provide upper and lower bounds on the semileptonic weak decay form factors for $B \\to D^(*)$ and $\\Lambda_b \\to \\Lambda_c$ decays by utilizing inclusive heavy quark effective theory sum rules. These bounds are calculated to second order in $\\Lambda_{QCD}/m_Q$ and first order in $\\alpha_s$. The $O(\\alpha_s^2 \\beta_0)$ corrections to the bounds at zero recoil are also presented.

Cheng-Wei Chiang

2000-09-18T23:59:59.000Z

368

Bounds on Heavy-to-Heavy Baryonic Form Factors  

E-Print Network (OSTI)

Upper and lower bounds are established on the Lambda_b -> Lambda_c semileptonic decay form factors by utilizing inclusive heavy-quark-effective-theory sum rules. These bounds are calculated to leading order in Lambda_QCD/m_Q and alpha_s. The O(alpha_s^2 beta_0) corrections to the bounds at zero recoil are also presented. Several form factor models used in the literature are compared with our bounds.

Cheng-Wei Chiang

1999-07-29T23:59:59.000Z

369

Bounds on Heavy-to-Heavy Baryonic Form Factors  

E-Print Network (OSTI)

Upper and lower bounds are established on the Lambda_b -> Lambda_c semileptonic decay form factors by utilizing inclusive heavy-quark-effective-theory sum rules. These bounds are calculated to leading order in Lambda_QCD/m_Q and alpha_s. The O(alpha_s^2 beta_0) corrections to the bounds at zero recoil are also presented. Several form factor models used in the literature are compared with our bounds.

Chiang, C W

2000-01-01T23:59:59.000Z

370

Heavy flavor production from photons and hadrons  

Science Conference Proceedings (OSTI)

The present state of the production and observation of hadrons containing heavy quarks or antiquarks as valence constituents, in reactions initiated by real and (space-like) virtual photon or by hadron beams is discussed. Heavy flavor production in e/sup +/e/sup -/ annihilation, which is well covered in a number of recent review papers is not discussed, and similarly, neutrino production is omitted due to the different (flavor-changing) mechanisms that are involved in those reactions. Heavy flavors from spacelike photons, heavy flavors from real photons, and heavy flavors from hadron-hadron collisions are discussed. (WHK)

Heusch, C.A.

1982-01-01T23:59:59.000Z

371

Electrically shielded enclosure with magnetically retained removable cover  

DOE Patents (OSTI)

Disclosed is an electrically shielded enclosure having electrical components therein and a removable electrically shielded cover over an opening in the enclosure with a magnetic securement mechanism provided to removably secure the cover to the enclosure in a manner which will provide easy access, yet also provide an electrical seal between the cover and the enclosure capable of preventing the passage of electrical radiation through the joint between the cover and the enclosure. Magnets are provided on the enclosure peripherally around the opening and facing the cover, and a ferromagnetic surface is provided on the mating surface of the cover facing the magnets, with a continuous electrical seal provided between the magnets and the ferromagnetic surface on the cover to prevent the leakage of electromagnetic radiation therethrough. In one embodiment the electrical seal includes a flexible metal casing or surface, which is attached to the enclosure and positioned between the magnets and the ferromagnetic surface on the cover, and which is sufficiently flexible to be capable of conforming to the ferromagnetic surface to provide an electrical seal between the cover and the enclosure. In another embodiment, the electrical seal includes a metal mesh associated with the enclosure and positioned between the magnets on the enclosure and the ferromagnetic surface on the cover. The metal mesh is also capable of conforming to the surface of the ferromagnetic surface to thereby provide an electrical seal between the cover and the enclosure.

Rivers, Craig J. (Livermore, CA); Lee, Roanne A. (San Francisco, CA); Jones, Glenn E. (Livermore, CA)

1996-01-01T23:59:59.000Z

372

Method for extracting copper, silver and related metals  

DOE Patents (OSTI)

A process for selectively extracting precious metals such as silver and gold concurrent with copper extraction from aqueous solutions containing the same. The process utilizes tetrathiamacrocycles and high molecular weight organic acids that exhibit a synergistic relationship when complexing with certain metal ions thereby removing them from ore leach solutions.

Moyer, B.A.; McDowell, W.J.

1987-10-23T23:59:59.000Z

373

Removing Barriers to Interdisciplinary Research  

E-Print Network (OSTI)

A significant amount of high-impact contemporary scientific research occurs where biology, computer science, engineering and chemistry converge. Although programmes have been put in place to support such work, the complex dynamics of interdisciplinarity are still poorly understood. In this paper we interrogate the nature of interdisciplinary research and how we might measure its "success", identify potential barriers to its implementation, and suggest possible mechanisms for removing these impediments.

Naomi Jacobs; Martyn Amos

2010-12-19T23:59:59.000Z

374

METHOD OF REMOVING STRONTIUM IONS  

DOE Patents (OSTI)

A method is given for removing trace amounts of Sr/sup 90/ from solutions. Phosphate ion is added to the solution and it is then brought into contact with a solid salt such as calcium carbonate which will react methathetically with the phosphate ion to form a salt such as calcium phosphate. During this reaction, strontium will be absorbed to a high degree within the newly formed lattice. (AEC)

Rhodes, D.W.; McHenry, J.R.; Ames, L.L. Jr.

1962-05-01T23:59:59.000Z

375

Zero sound in strange metals with hyperscaling violation from holography  

E-Print Network (OSTI)

Hyperscaling violating `strange metal' phase of heavy fermion compounds can be described holographically by probe D-branes in the background of a Lifshitz space-time (dynamical exponent $z$ and spatial dimensions $d$) with hyperscaling violation (corresponding exponent $\\theta$). Without the hyperscaling violation, strange metals are known to exhibit zero sound mode for $zheat and the null energy condition of the background dictate that $\\thetaconductivity of the systems and briefly comment on the results.

Parijat Dey; Shibaji Roy

2013-06-30T23:59:59.000Z

376

Thermostat Metals  

Science Conference Proceedings (OSTI)

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

377

METAL COMPOSITIONS  

DOE Patents (OSTI)

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

Seybolt, A.U.

1959-02-01T23:59:59.000Z

378

Removal of arsenic compounds from spent catecholated polymer  

DOE Patents (OSTI)

Described is a process for removing arsenic from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic bound to it from contacting petroliferous liquid as described above and involves: a. treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10 and, b. separating the solids and liquids from each other. Preferably the regeneration treatment is in two steps wherein step (a) is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, steps (a) and (b) are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1985-01-01T23:59:59.000Z

379

Surface impurity removal from DIII-D graphite tiles by boron carbide grit blasting  

SciTech Connect

During the latter half of 1992, the DIII-D tokamak at General Atomics (GA) underwent several modifications of its interior. One of the major tasks involved the removal of accumulated metallic impurities from the surface of the graphite tiles used to line the plasma facing surfaces inside of the tokamak. Approximately 1500 graphite tiles and 100 boron nitride tiles from the tokamak were cleaned to remove the metallic impurities. The cleaning process consisted of several steps: the removed graphite tiles were permanently marked, surface blasted using boron carbide (B{sub 4}C) grit media (approximately 37 {mu}m. diam.), ultrasonically cleaned in ethanol to remove loose dust, and outgassed at 1000{degrees}C. Tests were done using, graphite samples and different grit blaster settings to determine the optimum propellant and abrasive media pressures to remove a graphite layer approximately 40-50 {mu}m deep and yet produce a reasonably smooth finish. EDX measurements revealed that the blasting technique reduced the surface Ni, Cr, and Fe impurity levels to those of virgin graphite. In addition to the surface impurity removal, tritium monitoring was performed throughout the cleaning process. A bubbler system was set up to monitor the tritium level in the exhaust gas from the grit blaster unit. Surface wipes were also performed on over 10% of the tiles. Typical surface tritium concentrations of the tiles were reduced from about 500 dpm/100 cm{sup 2} to less than 80 dpm/100 cm{sup 2} following the cleaning. This tile conditioning, and the installation of additional graphite tiles to cover a high fraction of the metallic plasma facing surfaces, has substantially reduced metallic impurities in the plasma discharges which has allowed rapid recovery from a seven-month machine opening and regimes of enhanced plasma energy confinement to be more readily obtained. Safety issues concerning blaster operator exposure to carcinogenic metals and radioactive tritium will also be addressed.

Lee, R.L.; Hollerbach, M.A.; Holtrop, K.L.; Kellman, A.G.; Taylor, P.L.; West, W.P.

1993-11-01T23:59:59.000Z

380

Topological superconductivity and Majorana fermions in metallic surface states  

E-Print Network (OSTI)

Heavy metals, such as Au, Ag, and Pb, often have sharp surface states that are split by strong Rashba spin-orbit coupling. The strong spin-orbit coupling and two-dimensional nature of these surface states make them ideal ...

Potter, Andrew Cole

Note: This page contains sample records for the topic "heavy metals removal" 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

Natural gas: Removing the obstacles  

Science Conference Proceedings (OSTI)

Defining and then figuring out how to remove whatever obstacles may be blocking the wider use of natural gas was the purpose of a conference held early last month in Phoenix, Arizona. The unique, three-day event was jointly sponsored by the U.S. Department of Energy (DOE) and the National Association of Regulatory Utility Commissioners (NARUC). It drew an overflow crowd of more than 500, with a registration list that read like a Who's Who of the natural gas industry. This article summarizes some of the main points of this conference.

Romo, C.

1992-03-15T23:59:59.000Z

382

Material Removal and Disposition | National Nuclear Security...  

National Nuclear Security Administration (NNSA)

Removal and Disposition | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response...

383

Energy Conservation in Metals  

Science Conference Proceedings (OSTI)

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

384

Heavy-Ion Physics with CMS  

E-Print Network (OSTI)

This article presents a brief overview of the CMS experiment capabilities to study the hot and dense matter created in relativistic heavy-ion collisions. The CERN Large Hadron Collider will provide collisions of Pb nuclei at 5.5 TeV per nucleon. The CMS heavy ion group has developed a plethora of physics analyses addressing many important aspects of heavy-ion physics in preparation for a competitive and successful program.

Aneta Iordanova

2008-06-06T23:59:59.000Z

385

Heavy ions and string theory  

E-Print Network (OSTI)

We review a selection of recent developments in the application of ideas of string theory to heavy ion physics. Our topics divide naturally into equilibrium and non-equilibrium phenomena. On the non-equilibrium side, we discuss generalizations of Bjorken flow, numerical simulations of black hole formation in asymptotically anti-de Sitter geometries, equilibration in the dual field theory, and hard probes. On the equilibrium side, we summarize improved holographic QCD, extraction of transport coefficients, inclusion of chemical potentials, and approaches to the phase diagram. We close with some possible directions for future research.

Oliver DeWolfe; Steven S. Gubser; Christopher Rosen; Derek Teaney

2013-04-29T23:59:59.000Z

386

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

DOE Patents (OSTI)

A liquid-liquid extraction method for removing metals and hydrous metal colloids from waste streams is provided wherein said waste streams are contacted with a solvent system containing a water-in-oil microemulsion wherein the inverted micelles contain the extracted metal. A silicon alkoxide, either alone or in combination with other metal alkoxide compounds is added to the water-in-oil microemulsion, thereby allowing encapsulation of the extracted metal within a silicon oxide network. Lastly, the now-encapsulated metal is precipitated from the water-in-oil microemulsion phase to yield aggregates of metal-silicate particles having average. individual particle sizes of approximately 40 manometers.

Chaiko, D.J.

1993-01-01T23:59:59.000Z

387

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

DOE Patents (OSTI)

A liquid-liquid extraction method for removing metals and hydrous metal colloids from waste streams is provided wherein said waste streams are contacted with a solvent system containing a water-in-oil microemulsion wherein the inverted micelles contain the extracted metal. A silicon alkoxide, either alone or in combination with other metal alkoxide compounds is added to the water-in-oil microemulsion, thereby allowing encapsulation of the extracted metal within a silicon oxide network. Lastly, the now-encapsulated metal is precipitated from the water-in-oil microemulsion phase to yield aggregates of metal-silicate particles having average individual particle sizes of approximately 40 nanometers. 2 figs.

Chaiko, D.J.

1995-03-07T23:59:59.000Z

388

Isospin Splittings of Doubly Heavy Baryons  

SciTech Connect

The SELEX Collaboration has reported a very large isospin splitting of doubly charmed baryons. We show that this effect would imply that the doubly charmed baryons are very compact. One intriguing possibility is that such baryons have a linear geometry Q-q-Q where the light quark q oscillates between the two heavy quarks Q, analogous to a linear molecule such as carbon dioxide. However, using conventional arguments, the size of a heavy-light hadron is expected to be around 0.5 fm, much larger than the size needed to explain the observed large isospin splitting. Assuming the distance between two heavy quarks is much smaller than that between the light quark and a heavy one, the doubly heavy baryons are related to the heavy mesons via heavy quark-diquark symmetry. Based on this symmetry, we predict the isospin splittings for doubly heavy baryons including {Xi}{sub cc}, {Xi}{sub bb} and {Xi}{sub bc}. The prediction for the {Xi}{sub cc} is much smaller than the SELEX value. On the other hand, the {Xi}{sub bb} baryons are predicted to have an isospin splitting as large as (6.3 {+-} 1.7) MeV. An experimental study of doubly bottomed baryons is therefore very important to better understand the structure of baryons with heavy quarks.

Brodsky, Stanley J.; /SLAC; Guo, Feng-Kun; /Bonn U., HISKP /Bonn U.; Hanhart, Christoph; /Julich, Forschungszentrum /JCHP, Julich /IAS, Julich; Meissner, Ulf-G.; /Julich, Forschungszentrum /JCHP, Julich /IAS, Julich /Bonn U., HISKP /Bonn U.

2011-08-18T23:59:59.000Z

389

Heavy Duty Truck Engine Advancement Adoption  

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

petroleum consumption. According to the DOE Energy Information Administration's Annual Energy Outlook (AEO) 2009, U.S. heavy truck fuel consumption will increase 23 percent between...

390

Factorization for hadronic heavy quarkonium production  

E-Print Network (OSTI)

We briefly review several models of heavy quarkonium production in hadronic collisions, and discuss the status of QCD factorization for these production models.

Jian-Wei Qiu

2006-10-31T23:59:59.000Z

391

Recent Heavy Flavor Results at RHIC  

E-Print Network (OSTI)

We summarize the recent experimental results of heavy favor physics from the Relativistic Heavy Ion Collider (RHIC) in Brookhaven National Lab (BNL) at Long Island, New York, USA.We will discuss the directly reconstructed open charm mesons as well as electrons from heavy favor hadron decays. The charm and bottom quark production cross-sections have also been measured. We will also discuss JPsi and Upsilon states in p+p and heavy ion collisions. The studies described here were carried out and reported by the STAR and PHENIX collaborations at RHIC.

Wenqin Xu

2011-10-13T23:59:59.000Z

392

Heavy ion physics at the LHC  

E-Print Network (OSTI)

Heavy Ion Physics at the LHC ? R. VogtLaboratory, Berkeley, CA USA Physics Department, Universityfor addressing unique physics issues in a completely new

Vogt, R.

2004-01-01T23:59:59.000Z

393

DISPERSION HARDENING OF URANIUM METAL  

DOE Patents (OSTI)

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

Arbiter, W.

1963-01-15T23:59:59.000Z

394

Heavy Flavour results from Tevatron  

SciTech Connect

The CDF and D0 experiments finalize the analysis of their full statistics collected in the p{bar p} collisions at a center-of-mass energy of {radical}s = 1.96 TeV at the Fermilab Tevatron collider. This paper presents several new results on the properties of hadrons containing heavy b- and c-quarks obtained by both collaborations. These results include the search for the rare decays B{sup 0}, B{sub s}{sup 0} {yields} {mu}{sup +}{mu}{sup -} (CDF), the study of CP asymmetry in B{sub s} {yields} J{psi}{phi} decay (CDF, D0), the measurement of the like-sign dimuon charge asymmetry (D0), the measurement of CP asymmetry in D{sup 0} {yields} K{sup +}K{sup -} and D{sup 0} {yields} {pi}{sup +}{pi}{sup -} decays (CDF), and the new measurement of the B{sub s} {yields} D{sub s}{sup (*)+} D{sub s}{sup (*)-} branching fraction (CDF). Both experiments still expect to produce more results on the properties of heavy flavours.

Borissov, G.; /Lancaster U.

2012-06-01T23:59:59.000Z

395

THERMALLY SHIELDED MOISTURE REMOVAL DEVICE  

DOE Patents (OSTI)

An apparatus is presented for removing moisture from the air within tanks by condensation upon a cartridge containing liquid air. An insulating shell made in two halves covers the cartridge within the evacuated system. The shell halves are hinged together and are operated by a system of levers from outside the tank with the motion translated through a sylphon bellows to cover and uncover the cartridge. When the condensation of moisture is in process, the insulative shell is moved away from the liquid air cartridge, and during that part of the process when there is no freezing out of moisture, the shell halves are closed on the cell so thnt the accumulated frost is not evaporated. This insulating shell greatly reduces the consumption of liquid air in this condensation process.

Miller, O.E.

1958-08-26T23:59:59.000Z

396

Process for recovering evolved hydrogen enriched with at least one heavy hydrogen isotope  

DOE Patents (OSTI)

This invention relates to a separation means and method for enriching a hydrogen atmosphere with at least one heavy hydrogen isotope by using a solid titaniun alloy hydride. To this end, the titanium alloy hydride containing at least one metal selected from the group consisting of vanadium, chromium, manganese, molybdenum, iron, cobalt and nickel is contacted with a circulating gaseous flow of hydrogen containing at least one heavy hydrogen isotope at a temperature in the range of -20.degree. to +40.degree. C and at a pressure above the dissociation pressure of the hydrided alloy selectively to concentrate at least one of the isotopes of hydrogen in the hydrided metal alloy. The contacting is continued until equilibrium is reached, and then the gaseous flow is isolated while the temperature and pressure of the enriched hydride remain undisturbed selectively to isolate the hydride. Thereafter, the enriched hydrogen is selectively recovered in accordance with the separation factor (S.F.) of the alloy hydride employed.

Tanaka, John (Storrs, CT); Reilly, Jr., James J. (Bellport, NY)

1978-01-01T23:59:59.000Z

397

Melter Glass Removal and Dismantlement  

Science Conference Proceedings (OSTI)

The U.S. Department of Energy (DOE) has been using vitrification processes to convert high-level radioactive waste forms into a stable glass for disposal in waste repositories. Vitrification facilities at the Savannah River Site (SRS) and at the West Valley Demonstration Project (WVDP) are converting liquid high-level waste (HLW) by combining it with a glass-forming media to form a borosilicate glass, which will ensure safe long-term storage. Large, slurry fed melters, which are used for this process, were anticipated to have a finite life (on the order of two to three years) at which time they would have to be replaced using remote methods because of the high radiation fields. In actuality the melters useable life spans have, to date, exceeded original life-span estimates. Initial plans called for the removal of failed melters by placing the melter assembly into a container and storing the assembly in a concrete vault on the vitrification plant site pending size-reduction, segregation, containerization, and shipment to appropriate storage facilities. Separate facilities for the processing of the failed melters currently do not exist. Options for handling these melters include (1) locating a facility to conduct the size-reduction, characterization, and containerization as originally planned; (2) long-term storing or disposing of the complete melter assembly; and (3) attempting to refurbish the melter and to reuse the melter assembly. The focus of this report is to look at methods and issues pertinent to size-reduction and/or melter refurbishment in particular, removing the glass as a part of a refurbishment or to reduce contamination levels (thus allowing for disposal of a greater proportion of the melter as low level waste).

Richardson, BS

2000-10-31T23:59:59.000Z

398

Nitrogen removal from natural gas  

SciTech Connect

According to a 1991 Energy Information Administration estimate, U.S. reserves of natural gas are about 165 trillion cubic feet (TCF). To meet the long-term demand for natural gas, new gas fields from these reserves will have to be developed. Gas Research Institute studies reveal that 14% (or about 19 TCF) of known reserves in the United States are subquality due to high nitrogen content. Nitrogen-contaminated natural gas has a low Btu value and must be upgraded by removing the nitrogen. In response to the problem, the Department of Energy is seeking innovative, efficient nitrogen-removal methods. Membrane processes have been considered for natural gas denitrogenation. The challenge, not yet overcome, is to develop membranes with the required nitrogen/methane separation characteristics. Our calculations show that a methane-permeable membrane with a methane/nitrogen selectivity of 4 to 6 would make denitrogenation by a membrane process viable. The objective of Phase I of this project was to show that membranes with this target selectivity can be developed, and that the economics of the process based on these membranes would be competitive. Gas permeation measurements with membranes prepared from two rubbery polymers and a superglassy polymer showed that two of these materials had the target selectivity of 4 to 6 when operated at temperatures below - 20{degrees}C. An economic analysis showed that a process based on these membranes is competitive with other technologies for small streams containing less than 10% nitrogen. Hybrid designs combining membranes with other technologies are suitable for high-flow, higher-nitrogen-content streams.

1997-04-01T23:59:59.000Z

399

Heavy vehicle propulsion system materials program semiannual progress report for April 1998 thru September 1998  

DOE Green Energy (OSTI)

The purpose of the Heavy Vehicle Propulsion System Materials Program is the development of materials: ceramics, intermetallics, metal alloys, and metal and ceramic coatings, to support the dieselization of class 1--3 trucks to realize a 35{percent} fuel-economy improvement over current gasoline-fueled trucks and to support commercialization of fuel-flexible LE-55 low-emissions, high-efficiency diesel engines for class 7--8 trucks. The Office of Transportation Technologies, Office of Heavy Vehicle Technologies (OTT OHVT) has an active program to develop the technology for advanced LE-55 diesel engines with 55{percent} efficiency and low emissions levels of 2.0 g/bhp-h NO{sub x} and 0.05 g/bhp-h particulates. The goal is also for the LE-55 engine to run on natural gas with efficiency approaching that of diesel fuel. The LE-55 program is being completed in FY 1997 and, after approximately 10 years of effort, has largely met the program goals of 55{percent} efficiency and low emissions. However, the commercialization of the LE-55 technology requires more durable materials than those that have been used to demonstrate the goals. Heavy Vehicle Propulsion System Materials will, in concert with the heavy-duty diesel engine companies, develop the durable materials required to commercialize the LE-55 technologies.

Johnson, D.R.

1999-01-01T23:59:59.000Z

400

Mechanochemical processing for metals and metal alloys  

DOE Patents (OSTI)

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

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

2001-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Process for removal of sulfur compounds from fuel gases  

DOE Patents (OSTI)

Fuel gases such as those produced in the gasification of coal are stripped of sulfur compounds and particulate matter by contact with molten metal salt. The fuel gas and salt are intimately mixed by passage through a venturi or other constriction in which the fuel gas entrains the molten salt as dispersed droplets to a gas-liquid separator. The separated molten salt is divided into a major and a minor flow portion with the minor flow portion passing on to a regenerator in which it is contacted with steam and carbon dioxide as strip gas to remove sulfur compounds. The strip gas is further processed to recover sulfur. The depleted, minor flow portion of salt is passed again into contact with the fuel gas for further sulfur removal from the gas. The sulfur depleted, fuel gas then flows through a solid absorbent for removal of salt droplets. The minor flow portion of the molten salt is then recombined with the major flow portion for feed to the venturi.

Moore, Raymond H. (Richland, WA); Stegen, Gary E. (Richland, WA)

1978-01-01T23:59:59.000Z

402

UNITAR boosts cogeneration for heavy crude production  

SciTech Connect

The UNITAR/UNDP Information Center for Heavy Crude and Tar Sands publicized the favorable effect of cogeneration on the economics of generating steam for in situ recovery of heavy oil. Although cogeneration of electricity with the production of steam for heavy crude production is a rapidly growing activity in California, it is still unknown in other countries where heavy crude is produced. The study concentrated on two specific cases: a heavy crude cogeneration plant in Kern County in California and a heavy crude production plant at Wolf Lake in Alberta, Canada. A comparison of the two cases showed that due to the specific conditions in California, cogeneration can reduce, in this specific case, the cost of production of heavy crude by $4.80 per barrel whereas in the case of Wolf Lake, cogeneration would not be economic (electricity prices in relation to natural gas prices are much lower in Canada). One of the purposes of the UNITAR study was to direct attention in other countries producing heavy crude to the advantages of cogeneration.

Not Available

1987-03-01T23:59:59.000Z

403

Heavy Vehicle Technologies Program Retrospective and Outlook  

DOE Green Energy (OSTI)

OHVT Mission is to conduct, in collaboration with our heavy vehicle industry partners and their suppliers, a customer-focused national program to research and develop technologies that will enable trucks and other heavy vehicles to be more energy efficient and able to use alternative fuels while simultaneously reducing emissions.

James J. Eberhardt

1999-04-10T23:59:59.000Z

404

Electron-State Hybridization in Heavy-Fermion Systems  

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

Electron-State Hybridization in Heavy-Fermion Systems Electron-State Hybridization in Heavy-Fermion Systems Print Wednesday, 27 September 2006 00:00 Heavy-fermion systems are...

405

Liquid metal cooled divertor for ARIES  

Science Conference Proceedings (OSTI)

A liquid metal, Ga-cooled divertor design was completed for the double null ARIES-II divertor design. The design analysis indicated a surface heat flux removal capability of up to 15 MW/m{sup 2}, and its relative easy maintenance. Design issues of configuration, thermal hydraulics, thermal stresses, liquid metal loop and safety effects were evaluated. For coolant flow control, it was found that it is necessary to use some part of the blanket cooling ducts for the draining of liquid metal from the top divertor. In order to minimize the inventory of Ga, it was recommended that the liquid metal loop equipment should be located as close to the torus as possible. More detailed analysis of transient conditions especially under accident conditions was identified as an issue that will need to be addressed.

Muraviev, E. [Gosudarstvennyj Komitet po Ispol`zovaniyu Atomnoj Ehnergii SSSR, Moscow (Russian Federation). Inst. Atomnoj Ehnergii

1995-01-01T23:59:59.000Z

406

Research and Development Opportunities for Heavy Trucks  

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

1] 1] Introduction Heavy-duty long-haul trucks are critical to the movement of the Nation's freight. These vehicles, which currently consume about 10 percent of the Nation's oil, are characterized by high fuel consumption, fast market turnover, and rapid uptake of new technologies. Improving the fuel economy of Class 8 trucks will dramatically impact both fuel and cost savings. This paper describes the importance of heavy trucks to the Nation's economy, and its potential for fuel efficiency gains. Why Focus on Heavy Trucks? Large and Immediate Impact Investments in improving the fuel economy of heavy Class 8 trucks will result in large reduction in petroleum consumption within a short timeframe. While heavy-duty vehicles make up only 4% of the

407

Heavy photon search experiment at JLAB  

SciTech Connect

The Heavy Photon Search (HPS) experiment in Hall-B at Jefferson Lab will search for new heavy vector boson(s), aka "heavy photons", in the mass range of 20 MeV/c{sup 2} to 1000 MeV/c{sup 2} using the scattering of high energy, high intensity electron beams off a high Z target. The proposed measurements will cover the region of parameter space favored by the muon g-2 anomaly, and will explore a significant region of parameter space, not only at large couplings ({alpha}'/{alpha} > 10{sup -7}), but also in the regions of small couplings, down to {alpha}'/{alpha}~10{sup -10}. The excellent vertexing capability of the Si-tracker uniquely enables HPS to cover the small coupling region. Also, HPS will search for heavy photons in an alternative to the e{sup +} e{sup -} decay mode, in the heavy photon's decay to {mu}{sup +}{mu}{sup -}.

Stepanyan, Stepan [JLAB

2013-11-01T23:59:59.000Z

408

Helicity probabilities for heavy quark fragmentation into heavy-light excited mesons  

E-Print Network (OSTI)

After a brief review on how heavy quark symmetry constraints the helicity fragmentation probabilities for a heavy quark hadronizes into heavy-light hadrons, we present a heavy quark fragmentation model to extract the value for the Falk-Peskin probability $w_{3/2}$ describing the fragmentation of a heavy quark into a heavy-light meson whose light degrees of freedom have angular momentum ${3 \\over 2}$. We point out that this probability depends on the longitudinal momentum fraction $z$ of the meson and on its transverse momentum $p_\\bot$ relative to the jet axis. In this model, the light degrees of freedom prefer to have their angular momentum aligned transverse to, rather than along, the jet axis. Implications for the production of excited heavy mesons, like $D^{**}$ and $B^{**}$, are briefly discussed.

Tzu Chiang Yuan

1995-03-08T23:59:59.000Z

409

Spectroscopy of Very Heavy Elements  

Science Conference Proceedings (OSTI)

Advances in spectroscopic techniques have meant that heavy nuclei in the upper right-hand corner of the nuclear chart have become amenable to detailed study. This detailed spectroscopic data can provide a stringent test for current nuclear structure theories. Experiments to investigate the structure of nuclei in the region of {sup 254}No can yield information concerning moments of inertia, stability against fission with rotation, single-particle properties, excitation energies of two quasi-particle states, and so on. A brief overview of the techniques used and recent results from studies in the region of {sup 254}No are presented, along with a summary of future developments which will allow further advances to be made.

Greenlees, P. T.; Herzberg, R.-D.; Ketelhut, S.; Eeckhaudt, S.; Jakobsson, U.; Jones, P.; Julin, R.; Juutinen, S.; Leino, M.; Nyman, M.; Peura, P.; Rahkila, P.; Saren, J.; Scholey, C.; Sorri, J.; Uusitalo, J. [Department of Physics, University of Jyvaeskylae, FIN-40014 Jyvaeskylae (Finland); Ackermann, D.; Hessberger, F.-P. [GSI, D-64291 Darmstadt (Germany); Butler, P. A.; Gray-Jones, C. [Department of Physics, University of Liverpool, Oxford Street, Liverpool, L69 7ZE (United Kingdom)] (and others)

2008-05-12T23:59:59.000Z

410

HEAVY WATER MODERATED NEUTRONIC REACTOR  

DOE Patents (OSTI)

A nuclear reactor of the type which utilizes uranium fuel elements and a liquid coolant is described. The fuel elements are in the form of elongated tubes and are disposed within outer tubes extending through a tank containing heavy water, which acts as a moderator. The ends of the fuel tubes are connected by inlet and discharge headers, and liquid bismuth is circulated between the headers and through the fuel tubes for cooling. Helium is circulated through the annular space between the outer tubes in the tank and the fuel tubes to cool the water moderator to prevent boiling. The fuel tubes are covered with a steel lining, and suitable control means, heat exchange means, and pumping means for the coolants are provided to complete the reactor assembly.

Szilard, L.

1958-04-29T23:59:59.000Z

411

Part 3: Removal Action | Department of Energy  

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

3: Removal Action 3: Removal Action Part 3: Removal Action Question: When may removal actions be initiated? Answer: Removal actions may be initiated when DOE determines that the action will prevent, minimize, stabilize, or eliminate a risk to health or the environment. The NCP specifies that the determination that a risk to health or the environment is appropriate for removal action should be based on: actual or potential exposure of humans, animals, or the food chain the presence of contained hazardous substances that pose a threat of release the threat of migration of the hazardous substances the threat of fire or explosion the availability of an appropriate Federal or State response capability [section 300.415(b)(2)]. In essence, where DOE identifies a threat of exposure to or migration of

412

Electron-State Hybridization in Heavy-Fermion Systems  

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

Electron-State Hybridization in Heavy-Fermion Systems Print Heavy-fermion systems are characterized by electrons with extremely large effective masses. The corresponding...

413

Deformation Prediction of a Heavy Hydro Turbine Blade During ...  

Science Conference Proceedings (OSTI)

Presentation Title, Deformation Prediction of a Heavy Hydro Turbine Blade During ... Abstract Scope, Heavy hydro turbine castings are made of martensitic ...

414

Ferroelectric Plasma Source for Heavy Ion Beam Charge Neutralization  

E-Print Network (OSTI)

Heavy Ion Beam Driven Fusion Reactor Study”, KfK-3480,a possible heavy ion fusion reactor design [1]. The final

2005-01-01T23:59:59.000Z

415

Process for particulate removal from coal liquids  

DOE Patents (OSTI)

Suspended solid particulates are removed from liquefied coal products by first subjecting such products to hydroclone action for removal in the underflow of the larger size particulates, and then subjecting the overflow from said hydroclone action, comprising the residual finer particulates, to an electrostatic field in an electrofilter wherein such finer particulates are deposited in the bed of beads of dielectric material on said filter. The beads are periodically cleaned by backwashing to remove the accumulated solids.

Rappe, Gerald C. (Macungie, PA)

1983-01-01T23:59:59.000Z

416

Method for removing contaminants from plastic resin  

Science Conference Proceedings (OSTI)

A resin recycling method that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The method includes receiving the resin in container form. The containers are then ground into resin particles. The particles are exposed to a solvent, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. After separating the particles and the resin, a solvent removing agent is used to remove any residual solvent remaining on the resin particles after separation.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-12-09T23:59:59.000Z

417

Passive Core Decay Heat Removal Performance Guideline  

Science Conference Proceedings (OSTI)

Passive decay heat removal systems operate without pumps when normal heat removal systems are not available. Safety is ensured by confirming that an adequate thermal margin is provided to accommodate various operating conditions, design uncertainties, and degradation. Guidelines to ensure adequate thermal performance are provided for three different system configurations.This report introduces utility systems engineers to the design and operation of passive decay heat removal systems and ...

2013-11-26T23:59:59.000Z

418

Vietnam HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

NNSANews posted a photo: Vietnam HEU Removal A convoy escorting the last highly enriched uranium in Vietnam departs Dalat. Facebook Twitter Youtube Flickr Headlines Jul 23,...

419

System for removing contaminants from plastic resin  

DOE Patents (OSTI)

A resin recycling system that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The system includes receiving the resin in container form. A grinder grinds the containers into resin particles. The particles are exposed to a solvent in one or more solvent wash vessels, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. A separator is used to separate the resin particles and the solvent. The resin particles are then placed in solvent removing element where they are exposed to a solvent removing agent which removes any residual solvent remaining on the resin particles after separation.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee' s Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2010-11-23T23:59:59.000Z

420

Improved sulfur removal processes evaluated for IGCC  

SciTech Connect

An inherent advantage of Integrated Coal Gasification Combined Cycle (IGCC) electric power generation is the ability to easily remove and recover sulfur. During the last several years, a number of new, improved sulfur removal and recovery processes have been commercialized. An assessment is given of alternative sulfur removal processes for IGCC based on the Texaco coal gasifier. The Selexol acid gas removal system, Claus sulfur recovery, and SCOT tail gas treating are currently used in Texaco-based IGCC. Other processes considered are: Purisol, Sulfinol-M, Selefning, 50% MDEA, Sulften, and LO-CAT. 2 tables.

1986-12-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Method for Removing Precipitates in Biofuel  

ORNL 2010-G00619/jcn UT-B ID 200902314 Method for Removing Precipitates in Biofuel Technology Summary At ORNL the application of ultrasonic energy, or ...

422

Internal Controls Over Classified Computersand Classified Removable...  

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

Classified Removable Media at theLawrence Livermore National Laboratory, IG-0628 Computers are used extensively in the full range of operations at Lawrence Livermore National...

423

Removal of radioisotopes from waste solutions  

DOE Patents (OSTI)

The invention comprises removing radioisotopes from waste liquids or solutions by passing these through filters and through a column containing a suitable salt of phosphoric acid. (Official Gazette)

Kirby, H.W.

1973-10-01T23:59:59.000Z

424

Tritium Removal Facility High Tritium Distillation Simulation.  

E-Print Network (OSTI)

??A dynamic model was developed for the distillation mechanism of the Darlington Tritium Removal Facility. The model was created using the commercial software package MATLAB/Simulink.… (more)

Zahedi, Polad

2013-01-01T23:59:59.000Z

425

Dynamics of neutralizing electrons during the focusing of intense heavy ions beams inside a heavy fusion reactor chamber  

E-Print Network (OSTI)

beams inside a heavy ion fusion reactor chamber * Agustin F.of a Heavy Ion Fusion reactor heavily depends on the maximum

Lifschitz, Agustin F.; Maynard, Gilles; Vay, Jean-Luc; Lenglet, Andrian

2006-01-01T23:59:59.000Z

426

Dynamics of neutralizing electrons during the focusing of intense heavy ions beams inside a heavy fusion reactor chamber  

E-Print Network (OSTI)

beams inside a heavy ion fusion reactor chamber * Agustin F.efficiency of a Heavy Ion Fusion reactor heavily depends on

Lifschitz, Agustin F.; Maynard, Gilles; Vay, Jean-Luc; Lenglet, Andrian

2006-01-01T23:59:59.000Z

427

Process and apparatus for generating elemental sulfur and re-usable metal oxide from spent metal sulfide sorbents  

DOE Patents (OSTI)

A process and apparatus for generating elemental sulfur and re-usable metal oxide from spent metal-sulfur compound. Spent metal-sulfur compound is regenerated to re-usable metal oxide by moving a bed of spent metal-sulfur compound progressively through a single regeneration vessel having a first and second regeneration stage and a third cooling and purging stage. The regeneration is carried out and elemental sulfur is generated in the first stage by introducing a first gas of sulfur dioxide which contains oxygen at a concentration less than the stoichiometric amount required for complete oxidation of the spent metal-sulfur compound. A second gas containing sulfur dioxide and excess oxygen at a concentration sufficient for complete oxidation of the partially spent metal-sulfur compound, is introduced into the second regeneration stage. Gaseous sulfur formed in the first regeneration stage is removed prior to introducing the second gas into the second regeneration stage. An oxygen-containing gas is introduced into the third cooling and purging stage. Except for the gaseous sulfur removed from the first stage, the combined gases derived from the regeneration stages which are generally rich in sulfur dioxide and lean in oxygen, are removed from the regenerator as an off-gas and recycled as the first and second gas into the regenerator. Oxygen concentration is controlled by adding air, oxygen-enriched air or pure oxygen to the recycled off-gas.

Ayala, Raul E. (Clifton Park, NY); Gal, Eli (Lititz, PA)

1995-01-01T23:59:59.000Z

428

Catalytic Cracking of Gaseous Heavy Hydrocarbons by Ceramic Filters  

DOE Green Energy (OSTI)

The use of syngas from waste or biomass gasification to generate electricity is a way which is attracting increasing attention especially with regard to the demands of regenerable energy consumption and to the reduction of waste disposal. In order to feed the syngas to a gas motor or a gas turbine the gas has to be cleaned. In future also the coupling of biomass gasification with a fuel cell will be applied, which needs a very efficient gas cleaning. The decomposition of tars and the removal of particles from the gas are the key issues of gas cleaning. Up to now these two steps are performed in two separate units. Normally, the tars are decomposed in catalytic beds or honeycomb structures. The catalytic decomposition is achieved at temperatures between 750 C and 900 C depending on the catalyst used. Particles are removed by filtration of the hot gas. Filtration at high temperatures and with high efficiencies is possible when using ceramic filter elements. Ceramic hot gas filters are well established in advanced coal gasification, such as the integrated gasification combined cycle process, as well as in waste and biomass gasification and pyrolysis processes. Since the catalytic reaction requires high temperatures the gas has to be reheated after the particles are removed in the filter or the hot unfiltered gas has to flow through the catalytic unit. If the gas is filtered first, reheating of the gas stream is an additional cost factor. Furthermore, pipes downstream of the filter can be plugged, if the temperature of the gas falls below the condensation temperature of the heavy hydrocarbons. Using the second way of hot unfiltered gas flows through the catalytic unit, there is the problem of deactivation of the catalyst by deposition of dust at higher dust concentrations. At worst the catalytic unit can be plugged by dust deposition.

Heidenreich, S.; Nacken, M.; Walch, A.; Chudzinski, S.

2002-09-19T23:59:59.000Z

429

Reduction of metal oxides through mechanochemical processing  

DOE Patents (OSTI)

The low temperature reduction of a metal oxide using mechanochemical processing techniques. The reduction reactions are induced mechanically by milling the reactants. In one embodiment of the invention, titanium oxide TiO.sub.2 is milled with CaH.sub.2 to produce TiH.sub.2. Low temperature heat treating, in the range of 400.degree. C. to 700.degree. C., can be used to remove the hydrogen in the titanium hydride.

Froes, Francis H. (Moscow, ID); Eranezhuth, Baburaj G. (Moscow, ID); Senkov, Oleg N. (Moscow, ID)

2000-01-01T23:59:59.000Z

430

Metallic Glass II  

Science Conference Proceedings (OSTI)

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

431

Light Metals 2010  

Science Conference Proceedings (OSTI)

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

432

Bulk Metallic Glasses IX  

Science Conference Proceedings (OSTI)

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

433

Bulk Metallic Glasses XI  

Science Conference Proceedings (OSTI)

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

434

Principal Metals Online  

Science Conference Proceedings (OSTI)

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

435

Refractory Metals Committee  

Science Conference Proceedings (OSTI)

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

436

DISSOLUTION METHOD OF REMOVING BONDING AGENTS  

DOE Patents (OSTI)

A method is given for removing residual aluminumsilicon bonding agents from uranium slugs after the removal of aluminum coatings. To accomplish this the slug is immersed in an aqueous solution about 0.75 N in hydrofluoric acid and about 7 N in nitric acid.

Hyman, H.H.

1960-04-19T23:59:59.000Z

437

Method of removing contaminants from plastic resins  

DOE Patents (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee' s Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-11-18T23:59:59.000Z

438

Method for removing contaminants from plastic resin  

Science Conference Proceedings (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-12-30T23:59:59.000Z

439

Method of removing contaminants from plastic resins  

Science Conference Proceedings (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert,George W. (Harrisonville, MO); Hand,Thomas E. (Lee's Summit, MO); Delaurentiis,Gary M. (Jamestown, CA)

2007-08-07T23:59:59.000Z

440

Global Cut Framework for Removing Symmetries  

Science Conference Proceedings (OSTI)

In this paper, we propose a general technique for removing symmetries in CSPs during search. The idea is to record no-goods, during the exploration of the search tree, whose symmetric counterpart (if any) should be removed. The no-good, called Global ...

Filippo Focacci; Michela Milano

2001-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "heavy metals removal" 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

Application of the selective equipment removal system to D&D tasks  

SciTech Connect

The Selective Equipment Removal System has been designed as a generic and reconfigurable remote manipulation platform to demonstrate and evaluate mobile telerobotic concepts suitable for performing selective decontamination and dismantlement functions. Both radioactive and hazardous chemical environments dictate that human presence should be minimized in many of these activities. In addition, robotic deployment of large and heavy tools should improve safety of operation by limiting human proximity to tooling. Monotonous, repetitive, and high precision activities should also benefit by robotic completion. This paper discusses the development of the Selective Equipment Retrieval System and its remote manipulation platform, the Dual Arm Work Module, applicable tooling, and application to various decontamination and dismantlement tasks.

Noakes, M.W.; Hamel, W.R.; Dixon, W.E.

1995-02-01T23:59:59.000Z

442

COST OF MERCURY REMOVAL IN IGCC PLANTS  

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

Cost of Mercury Removal Cost of Mercury Removal in an IGCC Plant Final Report September 2002 Prepared for: The United States Department of Energy National Energy Technology Laboratory By: Parsons Infrastructure and Technology Group Inc. Reading, Pennsylvania Pittsburgh, Pennsylvania DOE Product Manager: Gary J. Stiegel DOE Task Manager: James R. Longanbach Principal Investigators: Michael G. Klett Russell C. Maxwell Michael D. Rutkowski PARSONS The Cost of Mercury Removal in an IGCC Plant Final Report i September 2002 TABLE OF CONTENTS Section Title Page 1 Summary 1 2 Introduction 3 3 Background 4 3.1 Regulatory Initiatives 4 3.2 Mercury Removal for Conventional Coal-Fired Plants 4 3.3 Mercury Removal Experience in Gasification 5 3.4 Variability of Mercury Content in Coal 6 4 Design Considerations 7 4.1 Carbon Bed Location

443

Using Metal Hydride to Store Hydrogen  

DOE Green Energy (OSTI)

Hydrogen is the lightest element. At ambient conditions on a volume basis it stores the least amount of energy compared to other fuel carriers such as natural gas and gasoline. For hydrogen to become a practical fuel carrier, a way must be found to increase its volumetric energy density to a practical level. Present techniques being developed include compressed gas, cryogenic liquid and absorbed solid. Each of these techniques has its advantages and disadvantages. And none of them appears to be satisfactory for use in a hydrogen economy. In the interim all of them are used for demonstration purposes. Metal hydrides store hydrogen in a solid form under moderate temperature and pressure that gives them a safety advantage. They require the least amount of energy to operate. Their stored hydrogen density is nearing that of liquid hydrogen. But they are heavy and the weight is their main disadvantage. Current usable metal hydrides can hold no more than about 1.8 percent hydrogen by weight. However much effort is underway to find lighter materials. These include other solid materials other than the traditional metal hydrides. Their operation is expected to be similar to that of metal hydride and can use the technology developed for metal hydrides.

Heung, L.K.

2003-03-12T23:59:59.000Z

444

A 3 MEGAJOULE HEAVY ION FUSION DRIVER  

E-Print Network (OSTI)

Research, Office of Inertia! Fusion, Research Division ofA 3 MEGAJOULE HEAVY ION FUSION DRIVER* A. Faltens, E. Hoyer,Research, Office of Inertial Fusion, Research Division of

Faltens, A.

2010-01-01T23:59:59.000Z

445

NUCLEAR STRUCTURE AND HEAVY-ION FUSION  

E-Print Network (OSTI)

Nuclear Structure and Heavy-Ton Fusion* A series of lecturesthe cross section for fusion in the experiments consideredEffects g in III. Subharrier Fusion Cross Sections for Light

Stokstad, R.G.

2010-01-01T23:59:59.000Z

446

Heavy hadrons in quark-gluon plasma  

SciTech Connect

We use the nonperturbative quark-antiquark potential derived within the Field Correlator Method and the screened Coulomb potential to calculate binding energies and melting temperatures of heavy mesons and baryons in the deconfined phase of quark-gluon plasma.

Narodetskii, I. M., E-mail: naro@itep.ru; Simonov, Yu. A.; Veselov, A. I. [Institute of Theoretical and Experimental Physics (Russian Federation)

2011-03-15T23:59:59.000Z

447

Hadron Production in Heavy Ion Collisions  

E-Print Network (OSTI)

We review hadron production in heavy ion collisions with emphasis on pion and kaon production at energies below 2 AGeV and on partonic collectivity at RHIC energies.

Helmut Oeschler; Hans Georg Ritter; Nu Xu

2009-08-12T23:59:59.000Z

448

Magnetism and superconductivity of heavy fermion matter  

E-Print Network (OSTI)

The interplay of magnetism and unconventional superconductivity (d singlet wave or p triplet wave) in strongly correlated electronic system (SCES) is discussed with recent examples found in heavy fermion compounds. A short presentation is given on the formation of the heavy quasiparticle with the two sources of a local and intersite enhancement for the effective mass. Two cases of the coexistence or repulsion of antiferromagnetism and superconductivity are given with CeIn3 and CeCoIn5. A spectacular example is the emergence of superconductivity in relatively strong itinerant ferromagnets UGe2 and URhGe. The impact of heavy fermion matter among other SCES as organic conductor or high TC oxide is briefly pointed out. Key words: heavy fermion, superconductivity, antiferromagnetism, ferromagnetism

J. Flouquet A; G. Knebel A; D. Braithwaite A; D. Aoki B; J. P. Brison C; F. Hardy A; A. Huxley A; S. Raymond A; B. Salce A; I. Sheikin D

2005-01-01T23:59:59.000Z

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