Sample records for isotopic separation process

  1. Apparatus and process for separating hydrogen isotopes

    DOE Patents [OSTI]

    Heung, Leung K; Sessions, Henry T; Xiao, Xin

    2013-06-25T23:59:59.000Z

    The apparatus and process for separating hydrogen isotopes is provided using dual columns, each column having an opposite hydrogen isotopic effect such that when a hydrogen isotope mixture feedstock is cycled between the two respective columns, two different hydrogen isotopes are separated from the feedstock.

  2. Laser isotope separation

    DOE Patents [OSTI]

    Robinson, C. Paul (Los Alamos, NM); Jensen, Reed J. (Los Alamos, NM); Cotter, Theodore P. (Munich, DE); Boyer, Keith (Los Alamos, NM); Greiner, Norman R. (Los Alamos, NM)

    1988-01-01T23:59:59.000Z

    A process and apparatus for separating isotopes by selective excitation of isotopic species of a volatile compound by tuned laser light. A highly cooled gas of the volatile compound is produced in which the isotopic shift is sharpened and defined. Before substantial condensation occurs, the cooled gas is irradiated with laser light precisely tuned to a desired wavelength to selectively excite a particular isotopic species in the cooled gas. The laser light may impart sufficient energy to the excited species to cause it to undergo photolysis, photochemical reaction or even to photoionize. Alternatively, a two-photon irradiation may be applied to the cooled gas to induce photolysis, photochemical reaction or photoionization. The process is particularly applicable to the separation of isotopes of uranium.

  3. Photochemical isotope separation

    DOE Patents [OSTI]

    Robinson, C. Paul (Los Alamos, NM); Jensen, Reed J. (Los Alamos, NM); Cotter, Theodore P. (Los Alamos, NM); Greiner, Norman R. (Los Alamos, NM); Boyer, Keith (Los Alamos, NM)

    1987-01-01T23:59:59.000Z

    A process for separating isotopes by selective excitation of isotopic species of a volatile compound by tuned laser light. A highly cooled gas of the volatile compound is produced in which the isotopic shift is sharpened and defined. Before substantial condensation occurs, the cooled gas is irradiated with laser light precisely tuned to a desired wavelength to selectively excite a particular isotopic species in the cooled gas. The laser light may impart sufficient energy to the excited species to cause it to undergo photochemical reaction or even to photoionize. Alternatively, a two-photon irradiation may be applied to the cooled gas to induce photochemical reaction or photoionization. The process is particularly applicable to the separation of isotopes of uranium and plutonium.

  4. Photochemical isotope separation

    DOE Patents [OSTI]

    Robinson, C.P.; Jensen, R.J.; Cotter, T.P.; Greiner, N.R.; Boyer, K.

    1987-04-28T23:59:59.000Z

    A process is described for separating isotopes by selective excitation of isotopic species of a volatile compound by tuned laser light. A highly cooled gas of the volatile compound is produced in which the isotopic shift is sharpened and defined. Before substantial condensation occurs, the cooled gas is irradiated with laser light precisely tuned to a desired wavelength to selectively excite a particular isotopic species in the cooled gas. The laser light may impart sufficient energy to the excited species to cause it to undergo photochemical reaction or even to photoionize. Alternatively, a two-photon irradiation may be applied to the cooled gas to induce photochemical reaction or photoionization. The process is particularly applicable to the separation of isotopes of uranium and plutonium. 8 figs.

  5. Chromatographic hydrogen isotope separation

    DOE Patents [OSTI]

    Aldridge, Frederick T. (Livermore, CA)

    1981-01-01T23:59:59.000Z

    Intermetallic compounds with the CaCu.sub.5 type of crystal structure, particularly LaNiCo.sub.4 and CaNi.sub.5, exhibit high separation factors and fast equilibrium times and therefore are useful for packing a chromatographic hydrogen isotope separation colum. The addition of an inert metal to dilute the hydride improves performance of the column. A large scale mutli-stage chromatographic separation process run as a secondary process off a hydrogen feedstream from an industrial plant which uses large volumes of hydrogen can produce large quantities of heavy water at an effective cost for use in heavy water reactors.

  6. Isotope separation by laser means

    DOE Patents [OSTI]

    Robinson, C. Paul (Los Alamos, NM); Jensen, Reed J. (Los Alamos, NM); Cotter, Theodore P. (Los Alamos, NM); Greiner, Norman R. (Los Alamos, NM); Boyer, Keith (Los Alamos, NM)

    1982-06-15T23:59:59.000Z

    A process for separating isotopes by selective excitation of isotopic species of a volatile compound by tuned laser light. A highly cooled gas of the volatile compound is produced in which the isotopic shift is sharpened and defined. Before substantial condensation occurs, the cooled gas is irradiated with laser light precisely tuned to a desired wavelength to selectively excite a particular isotopic species in the cooled gas. The laser light may impart sufficient energy to the excited species to cause it to undergo photochemical reaction or even to photoionize. Alternatively, a two-photon irradiation may be applied to the cooled gas to induce photochemical reaction or photoionization. The process is particularly applicable to the separation of isotopes of uranium and plutonium.

  7. Hybrid isotope separation scheme

    DOE Patents [OSTI]

    Maya, J.

    1991-06-18T23:59:59.000Z

    A method is described for yielding selectively a desired enrichment in a specific isotope including the steps of inputting into a spinning chamber a gas from which a scavenger, radiating the gas with a wave length or frequency characteristic of the absorption of a particular isotope of the atomic or molecular gas, thereby inducing a photochemical reaction between the scavenger, and collecting the specific isotope-containing chemical by using a recombination surface or by a scooping apparatus. 2 figures.

  8. Hybrid isotope separation scheme

    DOE Patents [OSTI]

    Maya, Jakob (Brookline, MA)

    1991-01-01T23:59:59.000Z

    A method of yielding selectively a desired enrichment in a specific isotope including the steps of inputting into a spinning chamber a gas from which a scavenger, radiating the gas with a wave length or frequency characteristic of the absorption of a particular isotope of the atomic or molecular gas, thereby inducing a photochemical reaction between the scavenger, and collecting the specific isotope-containing chemical by using a recombination surface or by a scooping apparatus.

  9. Atomic-vapor-laser isotope separation

    SciTech Connect (OSTI)

    Davis, J.I.

    1982-10-01T23:59:59.000Z

    This paper gives a brief history of the scientific considerations leading to the development of laser isotope separation (LIS) processes. The close relationship of LIS to the broader field of laser-induced chemical processes is evaluated in terms of physical criteria to achieve an efficient production process. Atomic-vapor LIS processes under development at Livermore are reviwed. 8 figures.

  10. Hydrogen isotope separation

    DOE Patents [OSTI]

    Bartlit, John R. (Los Alamos, NM); Denton, William H. (Abingdon, GB3); Sherman, Robert H. (Los Alamos, NM)

    1982-01-01T23:59:59.000Z

    A system of four cryogenic fractional distillation columns interlinked with two equilibrators for separating a DT and hydrogen feed stream into four product streams, consisting of a stream of high purity D.sub.2, DT, T.sub.2, and a tritium-free stream of HD for waste disposal.

  11. Automated product recovery in a Hg-196 photochemical isotope separation process

    DOE Patents [OSTI]

    Grossman, M.W.; Speer, R.

    1992-07-21T23:59:59.000Z

    A method of removing deposited product from a photochemical reactor used in the enrichment of [sup 196]Hg has been developed and shown to be effective for rapid re-cycling of the reactor system. Unlike previous methods relatively low temperatures are used in a gas and vapor phase process of removal. Importantly, the recovery process is understood in a quantitative manner so that scaling design to larger capacity systems can be easily carried out. 2 figs.

  12. Automated product recovery in a HG-196 photochemical isotope separation process

    DOE Patents [OSTI]

    Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA)

    1992-01-01T23:59:59.000Z

    A method of removing deposited product from a photochemical reactor used in the enrichment of .sup.196 Hg has been developed and shown to be effective for rapid re-cycling of the reactor system. Unlike previous methods relatively low temperatures are used in a gas and vapor phase process of removal. Importantly, the recovery process is understood in a quantitative manner so that scaling design to larger capacity systems can be easily carried out.

  13. Process for producing enriched uranium having a {sup 235}U content of at least 4 wt. % via combination of a gaseous diffusion process and an atomic vapor laser isotope separation process to eliminate uranium hexafluoride tails storage

    DOE Patents [OSTI]

    Horton, J.A.; Hayden, H.W. Jr.

    1995-05-30T23:59:59.000Z

    An uranium enrichment process capable of producing an enriched uranium, having a {sup 235}U content greater than about 4 wt. %, is disclosed which will consume less energy and produce metallic uranium tails having a lower {sup 235}U content than the tails normally produced in a gaseous diffusion separation process and, therefore, eliminate UF{sub 6} tails storage and sharply reduce fluorine use. The uranium enrichment process comprises feeding metallic uranium into an atomic vapor laser isotope separation process to produce an enriched metallic uranium isotopic mixture having a {sup 235} U content of at least about 2 wt. % and a metallic uranium residue containing from about 0.1 wt. % to about 0.2 wt. % {sup 235} U; fluorinating this enriched metallic uranium isotopic mixture to form UF{sub 6}; processing the resultant isotopic mixture of UF{sub 6} in a gaseous diffusion process to produce a final enriched uranium product having a {sup 235}U content of at least 4 wt. %, and up to 93.5 wt. % or higher, of the total uranium content of the product, and a low {sup 235}U content UF{sub 6} having a {sup 235}U content of about 0.71 wt. % of the total uranium content of the low {sup 235}U content UF{sub 6}; and converting this low {sup 235}U content UF{sub 6} to metallic uranium for recycle to the atomic vapor laser isotope separation process. 4 figs.

  14. Process for producing enriched uranium having a .sup.235 U content of at least 4 wt. % via combination of a gaseous diffusion process and an atomic vapor laser isotope separation process to eliminate uranium hexafluoride tails storage

    DOE Patents [OSTI]

    Horton, James A. (Livermore, CA); Hayden, Jr., Howard W. (Oakridge, TN)

    1995-01-01T23:59:59.000Z

    An uranium enrichment process capable of producing an enriched uranium, having a .sup.235 U content greater than about 4 wt. %, is disclosed which will consume less energy and produce metallic uranium tails having a lower .sup.235 U content than the tails normally produced in a gaseous diffusion separation process and, therefore, eliminate UF.sub.6 tails storage and sharply reduce fluorine use. The uranium enrichment process comprises feeding metallic uranium into an atomic vapor laser isotope separation process to produce an enriched metallic uranium isotopic mixture having a .sup.235 U content of at least about 2 wt. % and a metallic uranium residue containing from about 0.1 wt. % to about 0.2 wt. % .sup.235 U; fluorinating this enriched metallic uranium isotopic mixture to form UF.sub.6 ; processing the resultant isotopic mixture of UF.sub.6 in a gaseous diffusion process to produce a final enriched uranium product having a .sup.235 U content of at least 4 wt. %, and up to 93.5 wt. % or higher, of the total uranium content of the product, and a low .sup.235 U content UF.sub.6 having a .sup.235 U content of about 0.71 wt. % of the total uranium content of the low .sup.235 U content UF.sub.6 ; and converting this low .sup.235 U content UF.sub.6 to metallic uranium for recycle to the atomic vapor laser isotope separation process.

  15. Laser-assisted isotope separation of tritium

    DOE Patents [OSTI]

    Herman, Irving P. (Castro Valley, CA); Marling, Jack B. (Livermore, CA)

    1983-01-01T23:59:59.000Z

    Methods for laser-assisted isotope separation of tritium, using infrared multiple photon dissociation of tritium-bearing products in the gas phase. One such process involves the steps of (1) catalytic exchange of a deuterium-bearing molecule XYD with tritiated water DTO from sources such as a heavy water fission reactor, to produce the tritium-bearing working molecules XYT and (2) photoselective dissociation of XYT to form a tritium-rich product. By an analogous procedure, tritium is separated from tritium-bearing materials that contain predominately hydrogen such as a light water coolant from fission or fusion reactors.

  16. Laser isotope separation of erbium and other isotopes

    DOE Patents [OSTI]

    Haynam, Christopher A. (3035 Ferdale Ct., Pleasanton, CA 94566); Worden, Earl F. (117 Vereda del Ciervo, Diablo, CA 94528)

    1995-01-01T23:59:59.000Z

    Laser isotope separation is accomplished using at least two photoionization pathways of an isotope simultaneously, where each pathway comprises two or more transition steps. This separation method has been applied to the selective photoionization of erbium isotopes, particularly for the enrichment of .sup.167 Er. The hyperfine structure of .sup.167 Er was used to find two three-step photoionization pathways having a common upper energy level.

  17. Laser isotope separation of erbium and other isotopes

    DOE Patents [OSTI]

    Haynam, C.A.; Worden, E.F.

    1995-08-22T23:59:59.000Z

    Laser isotope separation is accomplished using at least two photoionization pathways of an isotope simultaneously, where each pathway comprises two or more transition steps. This separation method has been applied to the selective photoionization of erbium isotopes, particularly for the enrichment of {sup 167}Er. The hyperfine structure of {sup 167}Er was used to find two three-step photoionization pathways having a common upper energy level. 3 figs.

  18. Method of separating boron isotopes

    DOE Patents [OSTI]

    Jensen, Reed J. (Los Alamos, NM); Thorne, James M. (Provo, UT); Cluff, Coran L. (Provo, UT); Hayes, John K. (Salt Lake City, UT)

    1984-01-01T23:59:59.000Z

    A method of boron isotope enrichment involving the isotope preferential photolysis of (2-chloroethenyl)dichloroborane as the feed material. The photolysis can readily be achieved with CO.sub.2 laser radiation and using fluences significantly below those required to dissociate BCl.sub.3.

  19. Method of separating boron isotopes

    DOE Patents [OSTI]

    Jensen, R.J.; Thorne, J.M.; Cluff, C.L.

    1981-01-23T23:59:59.000Z

    A method of boron isotope enrichment involving the isotope preferential photolysis of (2-chloroethenyl)-dichloroborane as the feed material. The photolysis can readily by achieved with CO/sub 2/ laser radiation and using fluences significantly below those required to dissociate BCl/sub 3/.

  20. Electrochemical Isotope Effect and Lithium Isotope Separation Jay R. Black,

    E-Print Network [OSTI]

    Mcdonough, William F.

    results showing a large lithium isotope separation due to electrodeposition. The fractionation is tunable lithium were plated from solutions of 1 M LiClO4 in propylene carbonate (PC) on planar nickel electrodes

  1. Apparatus for separating and recovering hydrogen isotopes

    DOE Patents [OSTI]

    Heung, Leung K. (Aiken, SC)

    1994-01-01T23:59:59.000Z

    An apparatus for recovering hydrogen and separating its isotopes. The apparatus includes a housing bearing at least a fluid inlet and a fluid outlet. A baffle is disposed within the housing, attached thereto by a bracket. A hollow conduit is coiled about the baffle, in spaced relation to the baffle and the housing. The coiled conduit is at least partially filled with a hydride. The hydride can be heated to a high temperature and cooled to a low temperature quickly by circulating a heat transfer fluid in the housing. The spacing between the baffle and the housing maximizes the heat exchange rate between the fluid in the housing and the hydride in the conduit. The apparatus can be used to recover hydrogen isotopes (protium, deuterium and tritium) from gaseous mixtures, or to separate hydrogen isotopes from each other.

  2. Hydrogen isotope separation utilizing bulk getters

    DOE Patents [OSTI]

    Knize, Randall J. (Los Angeles, CA); Cecchi, Joseph L. (Lawrenceville, NJ)

    1990-01-01T23:59:59.000Z

    Tritium and deuterium are separated from a gaseous mixture thereof, derived from a nuclear fusion reactor or some other source, by providing a casing with a bulk getter therein for absorbing the gaseous mixture to produce an initial loading of the getter, partially desorbing the getter to produce a desorbed mixture which is tritium-enriched, pumping the desorbed mixture into a separate container, the remaining gaseous loading in the getter being deuterium-enriched, desorbing the getter to a substantially greater extent to produce a deuterium-enriched gaseous mixture, and removing the deuterium-enriched mixture into another container. The bulk getter may comprise a zirconium-aluminum alloy, or a zirconium-vanadium-iron alloy. The partial desorption may reduce the loading by approximately fifty percent. The basic procedure may be extended to produce a multistage isotope separator, including at least one additional bulk getter into which the tritium-enriched mixture is absorbed. The second getter is then partially desorbed to produce a desorbed mixture which is further tritium-enriched. The last-mentioned mixture is then removed from the container for the second getter, which is then desorbed to a substantially greater extent to produce a desorbed mixture which is deuterium-enriched. The last-mentioned mixture is then removed so that the cycle can be continued and repeated. The method of isotope separation is also applicable to other hydrogen isotopes, in that the method can be employed for separating either deuterium or tritium from normal hydrogen.

  3. Hydrogen isotope separation utilizing bulk getters

    DOE Patents [OSTI]

    Knize, Randall J. (Los Angeles, CA); Cecchi, Joseph L. (Lawrenceville, NJ)

    1991-01-01T23:59:59.000Z

    Tritium and deuterium are separated from a gaseous mixture thereof, derived from a nuclear fusion reactor or some other source, by providing a casing with a bulk getter therein for absorbing the gaseous mixture to produce an initial loading of the getter, partially desorbing the getter to produce a desorbed mixture which is tritium-enriched, pumping the desorbed mixture into a separate container, the remaining gaseous loading in the getter being deuterium-enriched, desorbing the getter to a substantially greater extent to produce a deuterium-enriched gaseous mixture, and removing the deuterium-enriched mixture into another container. The bulk getter may comprise a zirconium-aluminum alloy, or a zirconium-vanadium-iron alloy. The partial desorption may reduce the loading by approximately fifty percent. The basic procedure may be extended to produce a multistage isotope separator, including at least one additional bulk getter into which the tritium-enriched mixture is absorbed. The second getter is then partially desorbed to produce a desorbed mixture which is further tritium-enriched. The last-mentioned mixture is then removed from the container for the second getter, which is then desorbed to a substantially greater extent to produce a desorbed mixture which is deuterium-enriched. The last-mentioned mixture is then removed so that the cycle can be continued and repeated. The method of isotope separation is also applicable to other hydrogen isotopes, in that the method can be employed for separating either deuterium or tritium from normal hydrogen.

  4. Hydrogen isotope separation utilizing bulk getters

    DOE Patents [OSTI]

    Knize, R.J.; Cecchi, J.L.

    1991-08-20T23:59:59.000Z

    Tritium and deuterium are separated from a gaseous mixture thereof, derived from a nuclear fusion reactor or some other source, by providing a casing with a bulk getter therein for absorbing the gaseous mixture to produce an initial loading of the getter, partially desorbing the getter to produce a desorbed mixture which is tritium-enriched, pumping the desorbed mixture into a separate container, the remaining gaseous loading in the getter being deuterium-enriched, desorbing the getter to a substantially greater extent to produce a deuterium-enriched gaseous mixture, and removing the deuterium-enriched mixture into another container. The bulk getter may comprise a zirconium-aluminum alloy, or a zirconium-vanadium-iron alloy. The partial desorption may reduce the loading by approximately fifty percent. The basic procedure may be extended to produce a multistage isotope separator, including at least one additional bulk getter into which the tritium-enriched mixture is absorbed. The second getter is then partially desorbed to produce a desorbed mixture which is further tritium-enriched. The last-mentioned mixture is then removed from the container for the second getter, which is then desorbed to a substantially greater extent to produce a desorbed mixture which is deuterium-enriched. The last-mentioned mixture is then removed so that the cycle can be continued and repeated. The method of isotope separation is also applicable to other hydrogen isotopes, in that the method can be employed for separating either deuterium or tritium from normal hydrogen. 4 figures.

  5. Laser isotope separation by multiple photon absorption

    DOE Patents [OSTI]

    Robinson, C. Paul (Los Alamos, NM); Rockwood, Stephen D. (Los Alamos, NM); Jensen, Reed J. (Los Alamos, NM); Lyman, John L. (Los Alamos, NM); Aldridge, III, Jack P. (Los Alamos, NM)

    1987-01-01T23:59:59.000Z

    Multiple photon absorption from an intense beam of infrared laser light may be used to induce selective chemical reactions in molecular species which result in isotope separation or enrichment. The molecular species must have a sufficient density of vibrational states in its vibrational manifold that, is the presence of sufficiently intense infrared laser light tuned to selectively excite only those molecules containing a particular isotope, multiple photon absorption can occur. By this technique, for example, intense CO.sub.2 laser light may be used to highly enrich .sup.34 S in natural SF.sub.6 and .sup.11 B in natural BCl.sub.3.

  6. Laser isotope separation by multiple photon absorption

    DOE Patents [OSTI]

    Robinson, C.P.; Rockwood, S.D.; Jensen, R.J.; Lyman, J.L.; Aldridge, J.P. III.

    1987-04-07T23:59:59.000Z

    Multiple photon absorption from an intense beam of infrared laser light may be used to induce selective chemical reactions in molecular species which result in isotope separation or enrichment. The molecular species must have a sufficient density of vibrational states in its vibrational manifold that, is the presence of sufficiently intense infrared laser light tuned to selectively excite only those molecules containing a particular isotope, multiple photon absorption can occur. By this technique, for example, intense CO[sub 2] laser light may be used to highly enrich [sup 34]S in natural SF[sub 6] and [sup 11]B in natural BCl[sub 3]. 8 figs.

  7. EIS-0136: Special Isotope Separation Project Idaho National Engineering Laboratory, Idaho Falls, Idaho

    Broader source: Energy.gov [DOE]

    The U.S. Department of Energy developed this EIS to provide environmental input to the decision to construct the Special Isotope Separation Project which would allow for the processing of existing fuel-grade plutonium into weapons-grade plutonium using the Atomic Laser Isotope Separation process.

  8. Cyclic membrane separation process

    DOE Patents [OSTI]

    Nemser, Stuart M.

    2005-05-03T23:59:59.000Z

    A cyclic process for controlling environmental emissions of volatile organic compounds (VOC) from vapor recovery in storage and dispensing operations of liquids maintains a vacuum in the storage tank ullage. In the first part of a two-part cyclic process ullage vapor is discharged through a vapor recovery system in which VOC are stripped from vented gas with a selectively gas permeable membrane. In the second part, the membrane is inoperative while gas pressure rises in the ullage. In one aspect of this invention, a vacuum is drawn in the membrane separation unit thus reducing overall VOC emissions.

  9. Cyclic membrane separation process

    DOE Patents [OSTI]

    Bowser, John

    2004-04-13T23:59:59.000Z

    A cyclic process for controlling environmental emissions of volatile organic compounds (VOC) from vapor recovery in storage and dispensing operations of liquids maintains a vacuum in the storage tank ullage. In one of a two-part cyclic process ullage vapor is discharged through a vapor recovery system in which VOC are stripped from vented gas with a selectively gas permeable membrane. In the other part, the membrane is inoperative while gas pressure rises in the ullage. Ambient air is charged to the membrane separation unit during the latter part of the cycle.

  10. Mantle Helium And Carbon Isotopes In Separation Creek Geothermal...

    Open Energy Info (EERE)

    Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs, Three Sisters Area, Central Oregon- Evidence For Renewed Volcanic Activity Or A Long Term Steady State...

  11. Atomic vapor laser isotope separation of lead-210 isotope

    DOE Patents [OSTI]

    Scheibner, K.F.; Haynam, C.A.; Johnson, M.A.; Worden, E.F.

    1999-08-31T23:59:59.000Z

    An isotopically selective laser process and apparatus for removal of Pb-210 from natural lead that involves a one-photon near-resonant, two-photon resonant excitation of one or more Rydberg levels, followed by field ionization and then electrostatic extraction. The wavelength to the near-resonant intermediate state is counter propagated with respect to the second wavelength required to populate the final Rydberg state. This scheme takes advantage of the large first excited state cross section, and only modest laser fluences are required. The non-resonant process helps to avoid two problems: first, stimulated Raman Gain due to the nearby F=3/2 hyperfine component of Pb-207 and, second, direct absorption of the first transition process light by Pb-207. 5 figs.

  12. Atomic vapor laser isotope separation of lead-210 isotope

    DOE Patents [OSTI]

    Scheibner, Karl F. (Tracy, CA); Haynam, Christopher A. (Pleasanton, CA); Johnson, Michael A. (Pleasanton, CA); Worden, Earl F. (Diablo, CA)

    1999-01-01T23:59:59.000Z

    An isotopically selective laser process and apparatus for removal of Pb-210 from natural lead that involves a one-photon near-resonant, two-photon resonant excitation of one or more Rydberg levels, followed by field ionization and then electrostatic extraction. The wavelength to the near-resonant intermediate state is counter propagated with respect to the second wavelength required to populate the final Rydberg state. This scheme takes advantage of the large first excited state cross section, and only modest laser fluences are required. The non-resonant process helps to avoid two problems: first, stimulated Raman Gain due to the nearby F=3/2 hyperfine component of Pb-207 and, second, direct absorption of the first transition process light by Pb-207.

  13. Novel hybrid isotope separation scheme and apparatus

    DOE Patents [OSTI]

    Maya, Jakob (Brookline, MA)

    1991-01-01T23:59:59.000Z

    A method of yielding selectively a desired enrichment in a specific isotope including the steps of inputting into a spinning chamber a gas from which the specific isotope is to be isolated, radiating the gas with frequencies characteristic of the absorption of a particular isotope of the atomic or molecular gas, thereby inducing a photoionization reaction of the desired isotope, and collecting the specific isotope ion by suitable ion collection means.

  14. Novel hybrid isotope separation scheme and apparatus

    DOE Patents [OSTI]

    Maya, J.

    1991-06-18T23:59:59.000Z

    A method is described for yielding selectively a desired enrichment in a specific isotope including the steps of inputting into a spinning chamber a gas from which the specific isotope is to be isolated, radiating the gas with frequencies characteristic of the absorption of a particular isotope of the atomic or molecular gas, thereby inducing a photoionization reaction of the desired isotope, and collecting the specific isotope ion by suitable ion collection means. 3 figures.

  15. Isotopic Effect on Ion Mobility and Separation of Isotopomers...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Effect on Ion Mobility and Separation of Isotopomers by High-Field Ion Mobility Spectrometry . Isotopic Effect on Ion Mobility and Separation of Isotopomers by High-Field Ion...

  16. Hydrogen separation process

    DOE Patents [OSTI]

    Mundschau, Michael (Longmont, CO); Xie, Xiaobing (Foster City, CA); Evenson, IV, Carl (Lafayette, CO); Grimmer, Paul (Longmont, CO); Wright, Harold (Longmont, CO)

    2011-05-24T23:59:59.000Z

    A method for separating a hydrogen-rich product stream from a feed stream comprising hydrogen and at least one carbon-containing gas, comprising feeding the feed stream, at an inlet pressure greater than atmospheric pressure and a temperature greater than 200.degree. C., to a hydrogen separation membrane system comprising a membrane that is selectively permeable to hydrogen, and producing a hydrogen-rich permeate product stream on the permeate side of the membrane and a carbon dioxide-rich product raffinate stream on the raffinate side of the membrane. A method for separating a hydrogen-rich product stream from a feed stream comprising hydrogen and at least one carbon-containing gas, comprising feeding the feed stream, at an inlet pressure greater than atmospheric pressure and a temperature greater than 200.degree. C., to an integrated water gas shift/hydrogen separation membrane system wherein the hydrogen separation membrane system comprises a membrane that is selectively permeable to hydrogen, and producing a hydrogen-rich permeate product stream on the permeate side of the membrane and a carbon dioxide-rich product raffinate stream on the raffinate side of the membrane. A method for pretreating a membrane, comprising: heating the membrane to a desired operating temperature and desired feed pressure in a flow of inert gas for a sufficient time to cause the membrane to mechanically deform; decreasing the feed pressure to approximately ambient pressure; and optionally, flowing an oxidizing agent across the membrane before, during, or after deformation of the membrane. A method of supporting a hydrogen separation membrane system comprising selecting a hydrogen separation membrane system comprising one or more catalyst outer layers deposited on a hydrogen transport membrane layer and sealing the hydrogen separation membrane system to a porous support.

  17. Separation processes using expulsion from dilute supercritical solutions

    DOE Patents [OSTI]

    Cochran, Jr., Henry D. (Oak Ridge, TN)

    1993-01-01T23:59:59.000Z

    A process for separating isotopes as well as other mixtures by utilizing the behavior of dilute repulsive or weakly attractive elements of the mixtures as the critical point of the solvent is approached.

  18. Separation processes using expulsion from dilute supercritical solutions

    DOE Patents [OSTI]

    Cochran, H.D. Jr.

    1993-04-20T23:59:59.000Z

    A process is described for separating isotopes as well as other mixtures by utilizing the behavior of dilute repulsive or weakly attractive elements of the mixtures as the critical point of the solvent is approached.

  19. Isotope separation by selective photodissociation of glyoxal

    DOE Patents [OSTI]

    Marling, John B. (Pleasanton, CA)

    1976-01-01T23:59:59.000Z

    Dissociation products, mainly formaldehyde and carbon monoxide, enriched in a desired isotope of carbon, oxygen, or hydrogen are obtained by the selective photodissociation of glyoxal wherein glyoxal is subjected to electromagnetic radiation of a predetermined wavelength such that photon absorption excites and induces dissociation of only those molecules of glyoxal containing the desired isotope.

  20. Separation Processes, Second Edition

    E-Print Network [OSTI]

    King, C. Judson

    1980-01-01T23:59:59.000Z

    Styrene Process Distillation Column Design, in "Professors'in Styrene Process Distillation Column Design, in "Profes-considered an easy distillation column design problem, but

  1. Separation process using microchannel technology

    DOE Patents [OSTI]

    Tonkovich, Anna Lee (Dublin, OH); Perry, Steven T. (Galloway, OH); Arora, Ravi (Dublin, OH); Qiu, Dongming (Bothell, WA); Lamont, Michael Jay (Hilliard, OH); Burwell, Deanna (Cleveland Heights, OH); Dritz, Terence Andrew (Worthington, OH); McDaniel, Jeffrey S. (Columbus, OH); Rogers, Jr.; William A. (Marysville, OH); Silva, Laura J. (Dublin, OH); Weidert, Daniel J. (Lewis Center, OH); Simmons, Wayne W. (Dublin, OH); Chadwell, G. Bradley (Reynoldsburg, OH)

    2009-03-24T23:59:59.000Z

    The disclosed invention relates to a process and apparatus for separating a first fluid from a fluid mixture comprising the first fluid. The process comprises: (A) flowing the fluid mixture into a microchannel separator in contact with a sorption medium, the fluid mixture being maintained in the microchannel separator until at least part of the first fluid is sorbed by the sorption medium, removing non-sorbed parts of the fluid mixture from the microchannel separator; and (B) desorbing first fluid from the sorption medium and removing desorbed first fluid from the microchannel separator. The process and apparatus are suitable for separating nitrogen or methane from a fluid mixture comprising nitrogen and methane. The process and apparatus may be used for rejecting nitrogen in the upgrading of sub-quality methane.

  2. Three phase downhole separator process

    DOE Patents [OSTI]

    Cognata, Louis John (Baytown, TX)

    2008-06-24T23:59:59.000Z

    Three Phase Downhole Separator Process (TPDSP) is a process which results in the separation of all three phases, (1) oil, (2) gas, and (3) water, at the downhole location in the well bore, water disposal injection downhole, and oil and gas production uphole.

  3. Methane/nitrogen separation process

    DOE Patents [OSTI]

    Baker, R.W.; Lokhandwala, K.A.; Pinnau, I.; Segelke, S.

    1997-09-23T23:59:59.000Z

    A membrane separation process is described for treating a gas stream containing methane and nitrogen, for example, natural gas. The separation process works by preferentially permeating methane and rejecting nitrogen. The authors have found that the process is able to meet natural gas pipeline specifications for nitrogen, with acceptably small methane loss, so long as the membrane can exhibit a methane/nitrogen selectivity of about 4, 5 or more. This selectivity can be achieved with some rubbery and super-glassy membranes at low temperatures. The process can also be used for separating ethylene from nitrogen. 11 figs.

  4. Methane/nitrogen separation process

    DOE Patents [OSTI]

    Baker, Richard W. (Palo Alto, CA); Lokhandwala, Kaaeid A. (Menlo Park, CA); Pinnau, Ingo (Palo Alto, CA); Segelke, Scott (Mountain View, CA)

    1997-01-01T23:59:59.000Z

    A membrane separation process for treating a gas stream containing methane and nitrogen, for example, natural gas. The separation process works by preferentially permeating methane and rejecting nitrogen. We have found that the process is able to meet natural gas pipeline specifications for nitrogen, with acceptably small methane loss, so long as the membrane can exhibit a methane/nitrogen selectivity of about 4, 5 or more. This selectivity can be achieved with some rubbery and super-glassy membranes at low temperatures. The process can also be used for separating ethylene from nitrogen.

  5. Separation Process Economics

    E-Print Network [OSTI]

    Barron, T. S.; Wrobel, P. J.

    'M Coat Moderate 3. Freeze Crystallization processes Table 4. Curaet.ri.tic. Coat 11...nt H?? a _tal h.at .,,:hanq??urrae. bet....n the proe??a and the r.frig.ra:nt. ? equir?? -.eb.ni.. tor a??pln9 this ."rtae. tr.. he- ice d.po.ita which would...

  6. Standard practice for the ion exchange separation of uranium and plutonium prior to isotopic analysis

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2008-01-01T23:59:59.000Z

    Standard practice for the ion exchange separation of uranium and plutonium prior to isotopic analysis

  7. Efficient separations & processing crosscutting program

    SciTech Connect (OSTI)

    NONE

    1996-08-01T23:59:59.000Z

    The Efficient Separations and Processing Crosscutting Program (ESP) was created in 1991 to identify, develop, and perfect chemical and physical separations technologies and chemical processes which treat wastes and address environmental problems throughout the DOE complex. The ESP funds several multiyear tasks that address high-priority waste remediation problems involving high-level, low-level, transuranic, hazardous, and mixed (radioactive and hazardous) wastes. The ESP supports applied research and development (R & D) leading to the demonstration or use of these separations technologies by other organizations within the Department of Energy (DOE), Office of Environmental Management.

  8. Separation of the isotopes of boron by chemical exchange reactions

    DOE Patents [OSTI]

    McCandless, F.P.; Herbst, R.S.

    1995-05-30T23:59:59.000Z

    The isotopes of boron, {sup 10}B and {sup 11}B, are separated by means of a gas-liquid chemical exchange reaction involving the isotopic equilibrium between gaseous BF{sub 3} and a liquid BF{sub 3} donor molecular addition complex formed between BF{sub 3} gas and a donor chosen from the group consisting of: nitromethane, acetone, methyl isobutyl ketone, or diisobutyl ketone. 1 Fig.

  9. Continuous magnetic separator and process

    DOE Patents [OSTI]

    Oder, Robin R. (Export, PA); Jamison, Russell E. (Lower Burrell, PA)

    2008-04-22T23:59:59.000Z

    A continuous magnetic separator and process for separating a slurry comprising magnetic particles into a clarified stream and a thickened stream. The separator has a container with a slurry inlet, an overflow outlet for the discharge of the clarified slurry stream, and an underflow outlet for the discharge of a thickened slurry stream. Magnetic particles in the slurry are attracted to, and slide down, magnetic rods within the container. The slurry is thus separated into magnetic concentrate and clarified slurry. Flow control means can be used to control the ratio of the rate of magnetic concentrate to the rate of clarified slurry. Feed control means can be used to control the rate of slurry feed to the slurry inlet.

  10. A Mass Spectrometry Study of Isotope Separation in the Laser Plume

    E-Print Network [OSTI]

    Suen, Timothy Wu

    2012-01-01T23:59:59.000Z

    Zhang, and J. A. Nees, “Isotope Enrichment in Laser-AblationA. Naik, “Comment on “Isotope Enrichment in Laser-AblationP. Pronko, “Isotope separation and enrichment by ultrafast

  11. Advancement of isotope separation for the production of reference standards

    SciTech Connect (OSTI)

    Jared Horkley; Christopher McGrath; Andrew Edwards; Gaven Knighton; Kevin Carney; Jacob Davies; James Sommers; Jeffrey Giglio

    2012-03-01T23:59:59.000Z

    Idaho National Laboratory (INL) operates a mass separator that is currently producing high purity isotopes for use as internal standards for high precision isotope dilution mass spectrometry (IDMS). In 2008, INL began the revival of the vintage 1970’s era instrument. Advancements thus far include the successful upgrading and development of system components such as the vacuum system, power supplies, ion-producing components, and beam detection equipment. Progress has been made in the separation and collection of isotopic species including those of Ar, Kr, Xe, Sr, and Ba. Particular focuses on ion source improvements and developments have proven successful with demonstrated output beam currents of over 10 micro-amps 138Ba and 350nA 134Ba from a natural abundance source charge (approximately 2.4 percent 134Ba). In order to increase production and collection of relatively high quantities (mg levels) of pure isotopes, several advancements have been made in ion source designs, source material introduction, and beam detection and collection. These advancements and future developments will be presented.

  12. Development of Halide and Oxy-Halides for Isotopic Separations

    SciTech Connect (OSTI)

    Leigh R. Martin; Aaron T. Johnson; Jana Pfeiffer; Martha R. Finck

    2014-10-01T23:59:59.000Z

    The goal of this project was to synthesize a volatile form of Np for introduction into mass spectrometers at INL. Volatile solids of the 5f elements are typically those of the halides (e.g. UF6), however fluorine is highly corrosive to the sensitive internal components of the mass separator, and the other volatile halides exist as several different stable isotopes in nature. However, iodide is both mono-isotopic and volatile, and as such presents an avenue for creation of a form of Np suitable for introduction into the mass separator. To accomplish this goal, the technical work in the project sought to establish a novel synthetic route for the conversion NpO2+ (dissolved in nitric acid) to NpI3 and NpI4.

  13. NOVEL CONCEPTS FOR ISOTOPIC SEPARATION OF 3HE/4HE

    SciTech Connect (OSTI)

    Roy, L.; Nigg, H.; Watson, H.

    2012-09-04T23:59:59.000Z

    The research outlined below established theoretical proof-of-concept using ab initio calculations that {sup 3}He can be separated from {sup 4}He by taking advantage of weak van der Waals interactions with other higher molecular weight rare gases such as xenon. To the best of our knowledge, this is the only suggested method that exploits the physical differences of the isotopes using a chemical interaction.

  14. Separation Processes CHE 485, 3 Credits

    E-Print Network [OSTI]

    Fuchs, Alan

    such as: vapor pressure, solubility, adsorptivity and diffusivity. Examples of separations processes based and multistage equilibrium chemical processes ­ product recovery, purity and separation power, azeotropic systems Phenomena (CHE 374). Computer Usage CHEMCAD simulation software for design of unit operations processes

  15. Methods for separating medical isotopes using ionic liquids

    DOE Patents [OSTI]

    Luo, Huimin; Boll, Rose Ann; Bell, Jason Richard; Dai, Sheng

    2014-10-21T23:59:59.000Z

    A method for extracting a radioisotope from an aqueous solution, the method comprising: a) intimately mixing a non-chelating ionic liquid with the aqueous solution to transfer at least a portion of said radioisotope to said non-chelating ionic liquid; and b) separating the non-chelating ionic liquid from the aqueous solution. In preferred embodiments, the method achieves an extraction efficiency of at least 80%, or a separation factor of at least 1.times.10.sup.4 when more than one radioisotope is included in the aqueous solution. In particular embodiments, the method is applied to the separation of medical isotopes pairs, such as Th from Ac (Th-229/Ac-225, Ac-227/Th-227), or Ra from Ac (Ac-225 and Ra-225, Ac-227 and Ra-223), or Ra from Th (Th-227 and Ra-223, Th-229 and Ra-225).

  16. Integration of the AVLIS (atomic vapor laser isotopic separation) process into the nuclear fuel cycle. [Effect of AVLIS feed requirements on overall fuel cycle

    SciTech Connect (OSTI)

    Hargrove, R.S.; Knighton, J.B.; Eby, R.S.; Pashley, J.H.; Norman, R.E.

    1986-08-01T23:59:59.000Z

    AVLIS RD and D efforts are currently proceeding toward full-scale integrated enrichment demonstrations in the late 1980's and potential plant deployment in the mid 1990's. Since AVLIS requires a uranium metal feed and produces an enriched uranium metal product, some change in current uranium processing practices are necessitated. AVLIS could operate with a UF/sub 6/-in UF/sub 6/-out interface with little effect to the remainder of the fuel cycle. This path, however, does not allow electric utility customers to realize the full potential of low cost AVLIS enrichment. Several alternative processing methods have been identified and evaluated which appear to provide opportunities to make substantial cost savings in the overall fuel cycle. These alternatives involve varying levels of RD and D resources, calendar time, and technical risk to implement and provide these cost reduction opportunities. Both feed conversion contracts and fuel fabricator contracts are long-term entities. Because of these factors, it is not too early to start planning and making decisions on the most advantageous options so that AVLIS can be integrated cost effectively into the fuel cycle. This should offer economic opportunity to all parties involved including DOE, utilities, feed converters, and fuel fabricators. 10 refs., 11 figs., 2 tabs.

  17. Process for strontium-82 separation

    DOE Patents [OSTI]

    Heaton, R.C.; Jamriska, D.J. Sr.; Taylor, W.A.

    1992-12-01T23:59:59.000Z

    A process for selective separation of strontium-82 and strontium-85 from proton irradiated molybdenum targets comprises dissolving the molybdenum target in a hydrogen peroxide solution to form a first solution containing ions selected from a group consisting of molybdenum, niobium, technetium, selenium, vanadium, arsenic, germanium, zirconium, rubidium, zinc, beryllium, cobalt, iron, manganese, chromium, strontium, and yttrium; passing the solution through a first cationic resin whereby ions selected from a group consisting of zinc, beryllium, cobalt, iron, manganese, chromium, strontium, yttrium a portion of zirconium and a portion of rubidium are selectively absorbed by the first resin; contacting the first resin with an acid solution to strip and remove the absorbed ions from the first cationic exchange resin to form a second solution; evaporating the second solution for a time sufficient to remove substantially all of the acid and water from the solution whereby a residue remains; dissolving the residue in a dilute acid to form a third solution; passing the third solution through a second cationic resin whereby the ions are absorbed by the second resin; contacting the second resin with a dilute sulfuric acid solution whereby the absorbed ions selected from the group consisting of rubidium, zinc, beryllium, cobalt, iron, manganese, chromium and zirconium are selectively removed from the second resin; and contacting the second resin with a dilute acid solution whereby the absorbed strontium ions are selectively removed. 1 fig.

  18. Process for strontium-82 separation

    DOE Patents [OSTI]

    Heaton, Richard C. (Los Alamos, NM); Jamriska, Sr., David J. (Los Alamos, NM); Taylor, Wayne A. (Los Alamos, NM)

    1992-01-01T23:59:59.000Z

    A process for selective separation of strontium-82 and strontium-85 from proton irradiated molybdenum targets comprises dissolving the molybdenum target in a hydrogen peroxide solution to form a first solution containing ions selected from a group consisting of molybdenum, niobium, technetium, selenium, vanadium, arsenic, germanium, zirconium, rubidium, zinc, beryllium, cobalt, iron, manganese, chromium, strontium, and yttrium; passing the solution through a first cationic resin whereby ions selected from a group consisting of zinc, beryllium, cobalt, iron, manganese, chromium, strontium, yttrium a portion of zirconium and a portion of rubidium are selectively absorbed by the first resin; contacting the first resin with an acid solution to strip and remove the absorbed ions from the first cationic exchange resin to form a second solution; evaporating the second solution for a time sufficient to remove substantially all of the acid and water from the solution whereby a residue remains; dissolving the residue in a dilute acid to form a third solution; passing the third solution through a second cationic resin whereby the ions are absorbed by the second resin; contacting the second resin with a dilute sulfuric acid solution whereby the absorbed ions selected from the group consisting of rubidium, zinc, beryllium, cobalt, iron, manganese, chromium and zirconium are selectively removed from the second resin; and contacting the second resin with a dilute acid solution whereby the absorbed strontium ions are selectively removed.

  19. Separated isotopes: vital tools for science and medicine

    SciTech Connect (OSTI)

    Not Available

    1982-01-01T23:59:59.000Z

    Deliberations and conclusions of a Workshop on Stable Isotopes and Derived Radioisotopes organized by the Subcommittee on Nuclear and Radiochemistry of the National Research Council's Committee on Chemical Sciences at the request of the Department of Energy (DOE) are summarized. The workshop was jointly supported by the National Institutes of Health and DOE's Office of Basic Energy Sciences. An overview with three recommendations resulting from the Workshop is followed by reports of the four Workshop panels. Background papers were prepared by individuals on the Steering Committee and made available to all participants prior to the Workshop. They are reproduced as Appendixes 3 to 8. Short reports on alternate separation techniques were presented at the Workshop and are reproduced in Appendixes 9 to 11.

  20. Fabrication of Separator Demonstration Facility process vessel

    SciTech Connect (OSTI)

    Oberst, E.F.

    1985-01-15T23:59:59.000Z

    The process vessel system is the central element in the Separator Development Facility (SDF). It houses the two major process components, i.e., the laser-beam folding optics and the separators pods. This major subsystem is the critical-path procurement for the SDF project. Details of the vaious parts of the process vessel are given.

  1. Electrified Separation Processes in Industry

    E-Print Network [OSTI]

    Appleby, A. J.

    1983-01-01T23:59:59.000Z

    distillation, in the chemical and related industries is very considerable. The majority of the energy used for these separations is thermal input in the form of the low heating-value of oil or gas. From the national viewpoint, it would be advantageous...

  2. Liquid-phase thermal diffusion isotope separation apparatus and method having tapered column

    DOE Patents [OSTI]

    Rutherford, W.M.

    1985-12-04T23:59:59.000Z

    A thermal diffusion counterflow method and apparatus for separating isotopes in solution in which the solution is confined in a long, narrow, vertical slit which tapers from bottom to top. The variation in the width of the slit permits maintenance of a stable concentration distribution with relatively long columns, thus permitting isotopic separation superior to that obtained in the prior art.

  3. Analysis of gas centrifuge cascade for separation of multicomponent isotopes and optimal feed position

    SciTech Connect (OSTI)

    Chuntong Ying; Hongjiang Wu; Mingsheng Zhou; Yuguang Nie; Guangjun Liu [Tsinghua Univ., Beijing (China)

    1997-10-01T23:59:59.000Z

    Analysis of the concentration distribution in a gas centrifuge cascade for separation of multicomponent isotope mixtures is different from that in a cascade for separation of two-component mixtures. This paper presents the governing equations for a multicomponent isotope separation cascade. Numerically predicted separation factors for the gas centrifuge cascade agree well with the experimental data. A theoretical optimal feed position is derived for a short square cascade for a two-component mixture in a close-separation case. The optimal feed position for a gas centrifuge cascade for separation of multicomponent mixture is discussed.

  4. RAPID SEPARATION METHOD FOR 237NP AND PU ISOTOPES IN LARGE SOIL SAMPLES

    SciTech Connect (OSTI)

    Maxwell, S.; Culligan, B.; Noyes, G.

    2010-07-26T23:59:59.000Z

    A new rapid method for the determination of {sup 237}Np and Pu isotopes in soil and sediment samples has been developed at the Savannah River Site Environmental Lab (Aiken, SC, USA) that can be used for large soil samples. The new soil method utilizes an acid leaching method, iron/titanium hydroxide precipitation, a lanthanum fluoride soil matrix removal step, and a rapid column separation process with TEVA Resin. The large soil matrix is removed easily and rapidly using this two simple precipitations with high chemical recoveries and effective removal of interferences. Vacuum box technology and rapid flow rates are used to reduce analytical time.

  5. Packed bed reactor for photochemical sup 196 Hg isotope separation

    SciTech Connect (OSTI)

    Grossman, M.W.; Speer, R.

    1992-03-03T23:59:59.000Z

    This patent describes a photochemical reactor useful for the isotopic enrichment of a predetermined isotope of mercury comprising a reactor cell and a monoisotopic light source It comprises: a plurality of transparent, straight reactor cell tubes disposed axially within the internal volume of the reactor cell to increase the surface area thereof for production deposition.

  6. Process for separating nitrogen from methane using microchannel process technology

    DOE Patents [OSTI]

    Tonkovich, Anna Lee (Marysville, OH); Qiu, Dongming (Dublin, OH); Dritz, Terence Andrew (Worthington, OH); Neagle, Paul (Westerville, OH); Litt, Robert Dwayne (Westerville, OH); Arora, Ravi (Dublin, OH); Lamont, Michael Jay (Hilliard, OH); Pagnotto, Kristina M. (Cincinnati, OH)

    2007-07-31T23:59:59.000Z

    The disclosed invention relates to a process for separating methane or nitrogen from a fluid mixture comprising methane and nitrogen, the process comprising: (A) flowing the fluid mixture into a microchannel separator, the microchannel separator comprising a plurality of process microchannels containing a sorption medium, the fluid mixture being maintained in the microchannel separator until at least part of the methane or nitrogen is sorbed by the sorption medium, and removing non-sorbed parts of the fluid mixture from the microchannel separator; and (B) desorbing the methane or nitrogen from the sorption medium and removing the desorbed methane or nitrogen from the microchannel separator. The process is suitable for upgrading methane from coal mines, landfills, and other sub-quality sources.

  7. Delayed neutron studies of separated isotopes of Br, Rb, I, and Cs

    E-Print Network [OSTI]

    Reeder, R L; Wright, J F

    1976-01-01T23:59:59.000Z

    Discusses delayed neutron studies of separated isotopes of Br, Rb, I, and Cs are currently in progress at the Spectrometer for On-Line Analysis of Radionuclides (SOLAR) facility operated by Battelle, Pacific Northwest Laboratories. (2 refs).

  8. Resonance ionization laser ion sources for on-line isotope separators (invited)

    SciTech Connect (OSTI)

    Marsh, B. A. [EN Department, CERN, 1211 Geneva (Switzerland)] [EN Department, CERN, 1211 Geneva (Switzerland)

    2014-02-15T23:59:59.000Z

    A Resonance Ionization Laser Ion Source (RILIS) is today considered an essential component of the majority of Isotope Separator On Line (ISOL) facilities; there are seven laser ion sources currently operational at ISOL facilities worldwide and several more are under development. The ionization mechanism is a highly element selective multi-step resonance photo-absorption process that requires a specifically tailored laser configuration for each chemical element. For some isotopes, isomer selective ionization may even be achieved by exploiting the differences in hyperfine structures of an atomic transition for different nuclear spin states. For many radioactive ion beam experiments, laser resonance ionization is the only means of achieving an acceptable level of beam purity without compromising isotope yield. Furthermore, by performing element selection at the location of the ion source, the propagation of unwanted radioactivity downstream of the target assembly is reduced. Whilst advances in laser technology have improved the performance and reliability of laser ion sources and broadened the range of suitable commercially available laser systems, many recent developments have focused rather on the laser/atom interaction region in the quest for increased selectivity and/or improved spectral resolution. Much of the progress in this area has been achieved by decoupling the laser ionization from competing ionization processes through the use of a laser/atom interaction region that is physically separated from the target chamber. A new application of gas catcher laser ion source technology promises to expand the capabilities of projectile fragmentation facilities through the conversion of otherwise discarded reaction fragments into high-purity low-energy ion beams. A summary of recent RILIS developments and the current status of laser ion sources worldwide is presented.

  9. Process for recovery of daughter isotopes from a source material

    DOE Patents [OSTI]

    Tranter, Troy J.; Todd, Terry A.; Lewis, Leroy C.; Henscheid, Joseph P.

    2005-10-04T23:59:59.000Z

    The invention includes a method of separating isotopes from a mixture containing at least two isotopes in a solution. A first isotope is precipitated and is collected from the solution. A daughter isotope is generated and collected from the first isotope. The invention includes a method of producing an actinium-225/bismuth-213 product from a material containing thorium-229 and thorium-232. A solution is formed containing nitric acid and the material and iodate is added to form a thorium iodate precipitate. A supernatant is separated from the thorium iodate precipitate and a second volume of nitric acid is added to the precipitate. The precipitate is stored and a decay product comprising actinium-225 and bismuth-213 is generated in the second volume of nitric acid which is then separated from the thorium iodate precipitate, filtered, and treated using at least one chromatographic procedure. The invention also includes a system for producing an actinium-225/bismuth-213 product.

  10. Separation process using pervaporation and dephlegmation

    DOE Patents [OSTI]

    Vane, Leland M.; Mairal, Anurag P.; Ng, Alvin; Alvarez, Franklin R.; Baker, Richard W.

    2004-06-29T23:59:59.000Z

    A process for treating liquids containing organic compounds and water. The process includes a pervaporation step in conjunction with a dephlegmation step to treat at least a portion of the permeate vapor from the pervaporation step. The process yields a membrane residue stream, a stream enriched in the more volatile component (usually the organic) as the overhead stream from the dephlegmator and a condensate stream enriched in the less volatile component (usually the water) as a bottoms stream from the dephlegmator. Any of these may be the principal product of the process. The membrane separation step may also be performed in the vapor phase, or by membrane distillation.

  11. National uses and needs for separated stable isotopes in physics, chemistry, and geoscience research

    SciTech Connect (OSTI)

    Zisman, M.S.

    1982-01-01T23:59:59.000Z

    Present uses of separated stable isotopes in the fields of physics, chemistry, and the geosciences have been surveyed to identify current supply problems and to determine future needs. Demand for separated isotopes remains strong, with 220 different nuclides having been used in the past three years. The largest needs, in terms of both quantity and variety of isotopes, are found in nuclear physics research. Current problems include a lack of availability of many nuclides, unsatisfactory enrichment of rare species, and prohibitively high costs for certain important isotopes. It is expected that demands for separated isotopes will remain roughly at present levels, although there will be a shift toward more requests for highly enriched rare isotopes. Significantly greater use will be made of neutron-rich nuclides below A = 100 for producing exotic ion beams at various accelerators. Use of transition metal nuclei for nuclear magnetic resonance spectroscopy will expand. In addition, calibration standards will be required for the newer techniques of radiological dating, such as the Sm/Nd and Lu/Hf methods, but in relatively small quantities. Most members of the research community would be willing to pay considerably more than they do now to maintain adequate supplies of stable isotopes.

  12. Categorical Exclusion 4577: Lithium Isotope Separation & Enrichment Technologies

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645U.S. DOE Office511041clothAdvanced Materials Advanced. C o w l i t z C o . CForn1Categorical8/2012Lithium Isotope

  13. Practical-scale tests of cryogenic molecular sieve for separating low-concentration hydrogen isotopes from helium

    SciTech Connect (OSTI)

    Willms, R.S.; Taylor, D.J. [Los Alamos National Lab., NM (United States); Enoeda, M. [Japan Atomic Energy Research Inst., Ibaraki-ken (Japan)] [and others

    1994-12-31T23:59:59.000Z

    There are a number of cases in fusion fuel processing where low-concentration hydrogen isotopes need to be separated from helium. Usually the helium is a purge gas used to move hydrogen isotopes from one location to another. One of the most notable applications is associated with removing tritium from a solid ceramic breeder. For some designs which have been considered, helium with about 1 % protium is purged through the ceramic. The protium exchanges with tritium which has been bred in the solid. The resulting gas composed of helium ({approximately}99%), protium ({approximately}1%) and tritium ({approximately}0.01%) flows out of the blanket and, for further processing, requires separation of the hydrogen isotopes and the helium. Earlier bench-scale (about 50 cc of sieve) work at the Tritium Systems Test Assembly (TSTA) at Los Alamos National Laboratory examined a number of adsorbents for their suitability for separating low-concentration hydrogen (no tritium) from helium. One of the effective adsorbents was Linde 5A molecular sieve. The purpose of this paper is to report practical-scale experiments including tritium. These tests used existing cryogenic molecular sieve beds (MSB`S) which each contain about 1.6 kg of Linde 5A molecular sieve.

  14. Stable Isotope Protocols: Sampling and Sample Processing

    E-Print Network [OSTI]

    Levin, Lisa A; Currin, Carolyn

    2012-01-01T23:59:59.000Z

    plants, benthic microalgae [BMI], benthic macroalgae) andin a dessicator, prior to analysis. A.2 Benthic microalgaeBenthic microalgae (BMI) can be collected for isotope

  15. Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

    SciTech Connect (OSTI)

    Watkins, J.M.; DePaolo, D.J.; Ryerson, F.J.; Peterson, B.

    2011-03-01T23:59:59.000Z

    Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl{sub 2}Si{sub 2}O{sub 8}; denoted AN), albite (NaAlSi{sub 3}O{sub 8}; denoted AB), and diopside (CaMgSi{sub 2}O{sub 6}; denoted DI) were held at 1450°C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB–AN experiment, D{sub Ca}/D{sub Si} ~ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D{sub Ca}/D{sub Si} ~ 1. In the AB–DI experiment, D{sub Ca}/D{sub Si} ~ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB–AN experiment. In the AB–DI experiment, D{sub Mg}/D{sub Si} ~ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity—the ratio of the diffusivity of the cation (D{sub Ca}) to the diffusivity of silicon (D{sub Si}). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D{sub cation}/D{sub Si}. Cations diffusing in aqueous solutions display a similar relationship between isotopic separation efficiency and D{sub cation} =D{sub H 2 O} , although the efficiencies are smaller than in silicate liquids. Our empirical relationship provides a tool for predicting the magnitude of diffusive isotopic effects in many geologic environments and a basis for a more comprehensive theory of isotope separation in liquid solutions. We present a conceptual model for the relationship between diffusivity and liquid structure that is consistent with available data.

  16. Plutonium Chemistry in the UREX+ Separation Processes

    SciTech Connect (OSTI)

    ALena Paulenova; George F. Vandegrift, III; Kenneth R. Czerwinski

    2009-10-01T23:59:59.000Z

    The project "Plutonium Chemistry in the UREX+ Separation Processes” is led by Dr. Alena Paulenova of Oregon State University under collaboration with Dr. George Vandegrift of ANL and Dr. Ken Czerwinski of the University of Nevada at Las Vegas. The objective of the project is to examine the chemical speciation of plutonium in UREX+ (uranium/tributylphosphate) extraction processes for advanced fuel technology. Researchers will analyze the change in speciation using existing thermodynamics and kinetic computer codes to examine the speciation of plutonium in aqueous and organic phases. They will examine the different oxidation states of plutonium to find the relative distribution between the aqueous and organic phases under various conditions such as different concentrations of nitric acid, total nitrates, or actinide ions. They will also utilize techniques such as X-ray absorbance spectroscopy and small-angle neutron scattering for determining plutonium and uranium speciation in all separation stages. The project started in April 2005 and is scheduled for completion in March 2008.

  17. Isotope Development & Production | Nuclear Science | ORNL

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Medical Radioisotope Radiochemical Separation & Processing Strategic Isotope Production Super Heavy Element Discovery Nuclear Security Science & Technology Nuclear Systems...

  18. Process, including membrane separation, for separating hydrogen from hydrocarbons

    DOE Patents [OSTI]

    Baker, Richard W. (Palo Alto, CA); Lokhandwala, Kaaeid A. (Union City, CA); He, Zhenjie (Fremont, CA); Pinnau, Ingo (Palo Alto, CA)

    2001-01-01T23:59:59.000Z

    Processes for providing improved methane removal and hydrogen reuse in reactors, particularly in refineries and petrochemical plants. The improved methane removal is achieved by selective purging, by passing gases in the reactor recycle loop across membranes selective in favor of methane over hydrogen, and capable of exhibiting a methane/hydrogen selectivity of at least about 2.5 under the process conditions.

  19. Practical-scale tests of cryogenic molecular sieve for separating low-concentration hydrogen isotopes from helium

    SciTech Connect (OSTI)

    Willms, R.S.; Taylor, D.J. [Los Alamos National Lab., NM (United States); Enoeda, Mikio; Okuno, Kenji [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan)

    1994-06-01T23:59:59.000Z

    Earlier bench-scale work at the Tritium Systems Test Assembly (TSTA) at Los Alamos National Laboratory examined a number of adsorbents for their suitability for separating low-concentration hydrogen (no tritium) from helium. One of the effective adsorbents was Linde 5A molecular sieve. Recently, experiments including tritium were conducted using practical-scale adsorbers. These tests used existing cryogenic molecular sieve beds (CMSB`s) which each contain about 1.6 kg of Linde 5A molecular sieve. They are part of the TSTA integrated tritium processing system. Gas was fed to each CMSB at about 13 SLPM with a nominal composition of 99% He, 0.98% H{sub 2} and 0.02% HT. In all cases, for an extended period of time, the beds allowed no detectable (via Raman spectroscopy) hydrogen isotopes to escape in the bed effluent. Thereafter, the hydrogen isotopes appeared in the bed exit with a relatively sharp breakthrough curve. This work concludes that cryogenic molecular sieve adsorption is an practical and effective means of separating low-concentration hydrogen isotopes from a helium carrier.

  20. FY09 PROGRESS: MULTI-ISOTOPE PROCESS (MIP) MONITOR

    SciTech Connect (OSTI)

    Schwantes, Jon M.; Orton, Christopher R.; Fraga, Carlos G.; Christensen, Richard; Laspe, Amy R.; Ward, Rebecca M.

    2009-10-18T23:59:59.000Z

    Model and experimental estimates of the Multi-Isotope Process Monitor performance for determining burnup after dissolution and acid concentration during solvent extraction steps during reprocessing of spent nuclear fuel are presented.

  1. Process for exchanging hydrogen isotopes between gaseous hydrogen and water

    DOE Patents [OSTI]

    Hindin, Saul G. (Mendham, NJ); Roberts, George W. (Westfield, NJ)

    1980-08-12T23:59:59.000Z

    A process for exchanging isotopes of hydrogen, particularly tritium, between gaseous hydrogen and water is provided whereby gaseous hydrogen depeleted in tritium and liquid or gaseous water containing tritium are reacted in the presence of a metallic catalyst.

  2. Implications of Plutonium isotopic separation on closed fuel cycles and repository design

    SciTech Connect (OSTI)

    Forsberg, C. [Massachusetts Institute of Technology, 77 Massachusetts Ave. Cambridge, MA 20129 (United States)

    2013-07-01T23:59:59.000Z

    Advances in laser enrichment may enable relatively low-cost plutonium isotopic separation. This would have large impacts on LWR closed fuel cycles and waste management. If Pu-240 is removed before recycling plutonium as mixed oxide (MOX) fuel, it would dramatically reduce the buildup of higher plutonium isotopes, Americium, and Curium. Pu-240 is a fertile material and thus can be replaced by U-238. Eliminating the higher plutonium isotopes in MOX fuel increases the Doppler feedback, simplifies reactor control, and allows infinite recycle of MOX plutonium in LWRs. Eliminating fertile Pu-240 and Pu-242 reduces the plutonium content in MOX fuel and simplifies fabrication. Reducing production of Pu-241 reduces production of Am-241 - the primary heat generator in spent nuclear fuels after several decades. Reducing heat generating Am-241 would reduce repository cost and waste toxicity. Avoiding Am- 241 avoids its decay product Np-237, a nuclide that partly controls long-term oxidizing repository performance. Most of these benefits also apply to LWR plutonium recycled into fast reactors. There are benefits for plutonium isotopic separation in fast reactor fuel cycles (particularly removal of Pu-242) but the benefits are less. (author)

  3. Y-12 electromagnetic separation process wins approval

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    work immediately. Just like what we know of Groves, huh. The gaseous diffusion, reactor pile and electromagnetic separation approaches were reviewed with each group attempting to...

  4. Actinide and lanthanide separation process (ALSEP)

    DOE Patents [OSTI]

    Guelis, Artem V.

    2013-01-15T23:59:59.000Z

    The process of the invention is the separation of minor actinides from lanthanides in a fluid mixture comprising, fission products, lanthanides, minor actinides, rare earth elements, nitric acid and water by addition of an organic chelating aid to the fluid; extracting the fluid with a solvent comprising a first extractant, a second extractant and an organic diluent to form an organic extractant stream and an aqueous raffinate. Scrubbing the organic stream with a dicarboxylic acid and a chelating agent to form a scrubber discharge. The scrubber discharge is stripped with a simple buffering agent and a second chelating agent in the pH range of 2.5 to 6.1 to produce actinide and lanthanide streams and spent organic diluents. The first extractant is selected from bis(2-ethylhexyl)hydrogen phosphate (HDEHP) and mono(2-ethylhexyl)2-ethylhexyl phosphonate (HEH(EHP)) and the second extractant is selected from N,N,N,N-tetra-2-ethylhexyl diglycol amide (TEHDGA) and N,N,N',N'-tetraoctyl-3-oxapentanediamide (TODGA).

  5. Integration of advanced nuclear materials separation processes

    SciTech Connect (OSTI)

    Jarvinen, G.D.; Worl, L.A.; Padilla, D.D.; Berg, J.M.; Neu, M.P.; Reilly, S.D.; Buelow, S.

    1998-12-31T23:59:59.000Z

    This is the final report of a two-year, Laboratory Directed Research and Development (LDRD) project at the Los Alamos National Laboratory (LANL). This project has examined the fundamental chemistry of plutonium that affects the integration of hydrothermal technology into nuclear materials processing operations. Chemical reactions in high temperature water allow new avenues for waste treatment and radionuclide separation.Successful implementation of hydrothermal technology offers the potential to effective treat many types of radioactive waste, reduce the storage hazards and disposal costs, and minimize the generation of secondary waste streams. The focus has been on the chemistry of plutonium(VI) in solution with carbonate since these are expected to be important species in the effluent from hydrothermal oxidation of Pu-containing organic wastes. The authors investigated the structure, solubility, and stability of the key plutonium complexes. Installation and testing of flow and batch hydrothermal reactors in the Plutonium Facility was accomplished. Preliminary testing with Pu-contaminated organic solutions gave effluent solutions that readily met discard requirements. A new effort in FY 1998 will build on these promising initial results.

  6. Pollution prevention by process modification: Reactions and separations

    SciTech Connect (OSTI)

    Hopper, J.R.; Yaws, C.L.; Vichailak, M.; Ho, T.C. (Lamar Univ., Beaumont, TX (United States). Chemical Engineering Dept.)

    1994-01-01T23:59:59.000Z

    Pollution prevention by process modification of chemical process reaction and separation parameters is illustrated with case studies of four chemical processes. Each case has demonstrated the opportunities for minimizing waste products by applying the fundamentals of chemical engineering in the analysis of reactor design and separation parameters for each specific process. Two of the examples have resulted in commercial implementations.

  7. The JET Hydrogen-Oxygen Recombination Sensor – A Safety Device for Hydrogen Isotope Processing Systems

    E-Print Network [OSTI]

    The JET Hydrogen-Oxygen Recombination Sensor – A Safety Device for Hydrogen Isotope Processing Systems

  8. Process, including PSA and membrane separation, for separating hydrogen from hydrocarbons

    DOE Patents [OSTI]

    Baker, Richard W. (Palo Alto, CA); Lokhandwala, Kaaeid A. (Union City, CA); He, Zhenjie (Fremont, CA); Pinnau, Ingo (Palo Alto, CA)

    2001-01-01T23:59:59.000Z

    An improved process for separating hydrogen from hydrocarbons. The process includes a pressure swing adsorption step, a compression/cooling step and a membrane separation step. The membrane step relies on achieving a methane/hydrogen selectivity of at least about 2.5 under the conditions of the process.

  9. NATIONAL USES AND NEEDS FOR SEPARATED STABLE ISOTOPES IN PHYSICS, CHEMISTRY, AND GEOSCIENCE RESEARCH

    E-Print Network [OSTI]

    Zisman, M.S.

    2010-01-01T23:59:59.000Z

    of purchasing a low-enrichment isotope and having it furtherfour main areas: of isotopes, marginal enrichment and a highthe allowing isotope much interest enrichment into play, in

  10. Control structure selection for Reactor, Separator and Recycle Process

    E-Print Network [OSTI]

    Skogestad, Sigurd

    Control structure selection for Reactor, Separator and Recycle Process T. Larsson M.S. Govatsmark S to control", for a simple plant with a liquid phase reactor, a distillation column and recycle of unreacted processes is the presence of recycle. Variations of a plant with reaction, separation and mass recycle, see

  11. EVALUATION OF ALTERNATIVE STRONIUM AND TRANSURANIC SEPARATION PROCESSES

    SciTech Connect (OSTI)

    SMALLEY CS

    2011-04-25T23:59:59.000Z

    In order to meet contract requirements on the concentrations of strontium-90 and transuranic isotopes in the immobilized low-activity waste, strontium-90 and transuranics must be removed from the supernate of tanks 241-AN-102 and 241-AN-107. The process currently proposed for this application is an in-tank precipitation process using strontium nitrate and sodium permanganate. Development work on the process has not proceeded since 2005. The purpose of the evaluation is to identify whether any promising alternative processes have been developed since this issue was last examined, evaluate the alternatives and the baseline process, and recommend which process should be carried forward.

  12. Headquarters Separation Clearance Process | Department of Energy

    Energy Savers [EERE]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are being directed off Energy.gov.Energy02.pdf7 OPAM Flash2011-37 OPAMResourceEmployment VerificationSeparation

  13. Guidelines For Developing Low Energy Separation Processes

    E-Print Network [OSTI]

    Bojnowski, J. H.; Hanks, D. L.

    1981-01-01T23:59:59.000Z

    . 12) The efficiency of a process improves with increasing temperatures for heat above ambient and increases with decreasing temperatures for heat below ambient. CARNOT CYCLE ABOVE AMBIENT TO T Trreversible 4...

  14. Innovative lasers for uranium isotope separation. Final report, September 1, 1989--April 1, 1993

    SciTech Connect (OSTI)

    Brake, M.L.; Gilgenbach, R.M.

    1993-07-01T23:59:59.000Z

    Copper vapor laser have important applications to uranium atomic vapor laser isotope separation (AVLIS). We have investigated two innovative methods of exciting/pumping copper vapor lasers which have the potential to improve the efficiency and scaling of large laser systems used in uranium isotope separation. Experimental research has focused on the laser discharge kinetics of (1) microwave, and (2) electron beam excitation/pumping of large-volume copper vapor lasers. Microwave resonant cavity produced copper vapor plasmas at 2.45 GHz, have been investigated in three separate experimental configurations. The first examined the application of CW (0-500W) power and was found to be an excellent method for producing an atomic copper vapor from copper chloride. The second used a pulsed (5kW, 0.5--5 kHz) signal superimposed on the CW signal to attempt to produce vaporization, dissociation and excitation to the laser states. Enhanced emission of the optical radiation was observed but power densities were found to be too low to achieve lasing. In a third experiment we attempted to increase the applied power by using a high power magnetron to produce 100 kW of pulsed power. Unfortunately, difficulties with the magnetron power supply were encountered leaving inconclusive results. Detailed modeling of the electromagnetics of the system were found to match the diagnostics results well. An electron beam pumped copper vapor system (350 kV, 1.0 kA, 300 ns) was investigated in three separate copper chloride heating systems, external chamber, externally heated chamber and an internally heated chamber. Since atomic copper spectral lines were not observed, it is assumed that a single pulse accelerator is not capable of both dissociating the copper chloride and exciting atomic copper and a repetitively pulsed electron beam generator is needed.

  15. OPTIMAL SYNTHESIS, DESIGN AND OPERATION OF HYBRID SEPARATION PROCESSES

    E-Print Network [OSTI]

    Blandford, Ann

    or low relative volatilities. In a hybrid process where a distillation column unit and a pervaporation was to study the optimal configuration, design and operation of hybrid distillation/ membrane processes takingOPTIMAL SYNTHESIS, DESIGN AND OPERATION OF HYBRID SEPARATION PROCESSES Taj*alasfiaM. M. Barakat

  16. ISOTOPES

    E-Print Network [OSTI]

    Lederer, C. Michael

    2013-01-01T23:59:59.000Z

    rare (0.017%) isotope 36s at enrichments of 70% at a price32). The enrichment of carbon isotopes by C02-carbamatesulfur isotopes by S02-NaHS03 exchange and the enrichment of

  17. The beam diagnostic instruments in Beijing radioactive ion-beam facilities isotope separator on-line

    SciTech Connect (OSTI)

    Ma, Y., E-mail: yjma@ciae.ac.cn; Cui, B.; Ma, R.; Tang, B.; Chen, L.; Huang, Q.; Jiang, W. [China Institute of Atomic Energy, Beijing 102413 (China)] [China Institute of Atomic Energy, Beijing 102413 (China)

    2014-02-15T23:59:59.000Z

    The beam diagnostic instruments for Beijing Radioactive Ion-beam Facilities Isotope Separator On-Line are introduced [B. Q. Cui, Z. H. Peng, Y. J. Ma, R. G. Ma, B. Tang, T. Zhang, and W. S. Jiang, Nucl. Instrum. Methods 266, 4113 (2008); T. J. Zhang, X. L. Guan, and B. Q. Cui, in Proceedings of APAC 2004, Gyeongju, Korea, 2004, http://www.jacow.org , p. 267]. For low intensity ion beam [30–300 keV/1 pA–10 ?A], the beam profile monitor, the emittance measurement unit, and the analyzing slit will be installed. For the primary proton beam [100 MeV/200 ?A], the beam profile scanner will be installed. For identification of the nuclide, a beam identification unit will be installed. The details of prototype of the beam diagnostic units and some experiment results will be described in this article.

  18. Experimental Validation of the Multi-Isotope Process Monitor Concept

    SciTech Connect (OSTI)

    Orton, Christopher R.; Schwantes, Jon M.; Fraga, Carlos G.; Douglas, Matthew; Christensen, Richard

    2010-05-13T23:59:59.000Z

    Researchers from Pacific Northwest National Laboratory, in conjunction with personnel from The Ohio State University, are working to develop a system for monitoring spent nuclear fuel reprocessing facilities on-line, non-destructively, and in near-real-time. This method, known as the Multi-Isotope Process (MIP) Monitor, is based upon the measurement of distribution patterns of a suite of indicator (radioactive) isotopes present within particular process streams. Distribution patterns, monitored on-line by gamma spectrometry, are then compared in near-real-time to patterns representing "normal" process conditions using multivariate pattern recognition software. By targeting gamma-emitting indicator isotopes, the MIP Monitor approach is compatible with the use of small, portable, high-resolution gamma detectors that may be easily deployed throughout the facility. In addition, utilization of a suite of radio-elements, including ones with multiple oxidation states, increases the likelihood that attempts to divert material via process manipulation would be detected. Proof-of-principle modeling exercises simulating changes in acid strength have been completed and the results are promising. Laboratory validation is currently under way and significant results are available. The latest experimental results, along with an overview of the method will be presented.

  19. Magnetically activated and guided isotope separation This article has been downloaded from IOPscience. Please scroll down to see the full text article.

    E-Print Network [OSTI]

    Raizen, Mark G.

    The world relies today on enriched isotopes for medicine, basic science and energy, and the need will only excitation, and similarly requires high-power lasers. A lower power laser isotope enrichment (LIE) methodMagnetically activated and guided isotope separation This article has been downloaded from

  20. Process for preparing a chemical compound enriched in isotope content

    DOE Patents [OSTI]

    Michaels, Edward D. (Spring Valley, OH)

    1982-01-01T23:59:59.000Z

    A process to prepare a chemical enriched in isotope content which includes: (a) A chemical exchange reaction between a first and second compound which yields an isotopically enriched first compound and an isotopically depleted second compound; (b) the removal of a portion of the first compound as product and the removal of a portion of the second compound as spent material; (c) the conversion of the remainder of the first compound to the second compound for reflux at the product end of the chemical exchange reaction region; (d) the conversion of the remainder of the second compound to the first compound for reflux at the spent material end of the chemical exchange region; and the cycling of the additional chemicals produced by one conversion reaction to the other conversion reaction, for consumption therein. One of the conversion reactions is an oxidation reaction, and the energy that it yields is used to drive the other conversion reaction, a reduction. The reduction reaction is carried out in a solid polymer electrolyte electrolytic reactor. The overall process is energy efficient and yields no waste by-products.

  1. Sulfur isotopes as indicators of amended bacterial sulfate reduction processes influencing field scale uranium bioremediation

    E-Print Network [OSTI]

    Druhan, J.L.

    2009-01-01T23:59:59.000Z

    results in enrichment of S, the heavier isotope of sulfur,isotope data from M-24 were observed, although the degree of enrichmentisotopes as indicators of in situ acetate amended sulfate and uranium bioreduction processes. Enrichment

  2. The plasma centrifuge: A compact, low cost, stable isotope separator. Phase 2 final technical report, September 15, 1991--September 14, 1995

    SciTech Connect (OSTI)

    Guss, W.

    1996-09-05T23:59:59.000Z

    Enriched stable isotopes are required for production of radionuclides as well as for research and diagnostic uses. Science Research Laboratory (SRL) has developed a plasma centrifuge for moderate throughput of enriched stable isotopes, such as {sup 13}C, {sup 17}O, {sup 18}O, and {sup 203}Tl, for medical as well as other applications. Dwindling isotope stocks have restricted the use of enriched isotopes and their associated labeled organic molecules in medical imaging to very few research facilities because of high costs of isotope separation. With the introduction of the plasma centrifuge separator, the cost per separated gram of even rarely occurring isotopes ({le} 1% natural abundance) is potentially many times lower than with other separation technologies (cryogenic distillation and calutrons). The centrifuge is a simple, robust, pulsed electrical discharge device that has successfully demonstrated isotope separation of small (mg) quantities of {sup 26}Mg. Based on the results of the Phase 2 program, modest enhancements to the power supplies and cooling systems, a centrifuge separator will have high repetition rate (60 pps) and high duty cycle (60%) to produce in one month kilogram quantities of highly enriched stable isotopes. The centrifuge may be used in stand-alone operation or could be used as a high-throughput pre-separation stage with calutrons providing the final separation.

  3. Efficient Separations and Processing Crosscutting Program. Technology summary

    SciTech Connect (OSTI)

    NONE

    1995-06-01T23:59:59.000Z

    The Efficient Separations and Processing (ESP) Crosscutting Program was created in 1991 to identify, develop, and perfect separations technologies and processes to treat wastes and address environmental problems throughout the DOE Complex. The ESP funds several multi-year tasks that address high-priority waste remediation problems involving high-level, low-level, transuranic, hazardous, and mixed (radioactive and hazardous) wastes. The ESP supports applied research and development (R and D) leading to demonstration or use of these separations technologies by other organizations within DOE-EM. Treating essentially all DOE defense wastes requires separation methods that concentrate the contaminants and/or purify waste streams for release to the environment or for downgrading to a waste form less difficult and expensive to dispose of. Initially, ESP R and D efforts focused on treatment of high-level waste (HLW) from underground storage tanks (USTs) because of the potential for large reductions in disposal costs and hazards. As further separations needs emerge and as waste management and environmental restoration priorities change, the program has evolved to encompass the breadth of waste management and environmental remediation problems.

  4. Process to remove actinides from soil using magnetic separation

    DOE Patents [OSTI]

    Avens, Larry R. (Los Alamos, NM); Hill, Dallas D. (Los Alamos, NM); Prenger, F. Coyne (Los Alamos, NM); Stewart, Walter F. (Las Cruces, NM); Tolt, Thomas L. (Los Alamos, NM); Worl, Laura A. (Los Alamos, NM)

    1996-01-01T23:59:59.000Z

    A process of separating actinide-containing components from an admixture including forming a slurry including actinide-containing components within an admixture, said slurry including a dispersion-promoting surfactant, adjusting the pH of the slurry to within a desired range, and, passing said slurry through a pretreated matrix material, said matrix material adapted to generate high magnetic field gradients upon the application of a strong magnetic field exceeding about 0.1 Tesla whereupon a portion of said actinide-containing components are separated from said slurry and remain adhered upon said matrix material is provided.

  5. Automated process for solvent separation of organic/inorganic substance

    DOE Patents [OSTI]

    Schweighardt, Frank K. (Upper Macungie, PA)

    1986-01-01T23:59:59.000Z

    There is described an automated process for the solvent separation of organic/inorganic substances that operates continuously and unattended and eliminates potential errors resulting from subjectivity and the aging of the sample during analysis. In the process, metered amounts of one or more solvents are passed sequentially through a filter containing the sample under the direction of a microprocessor control apparatus. The mixture in the filter is agitated by ultrasonic cavitation for a timed period and the filtrate is collected. The filtrate of each solvent extraction is collected individually and the residue on the filter element is collected to complete the extraction process.

  6. Automated process for solvent separation of organic/inorganic substance

    DOE Patents [OSTI]

    Schweighardt, F.K.

    1986-07-29T23:59:59.000Z

    There is described an automated process for the solvent separation of organic/inorganic substances that operates continuously and unattended and eliminates potential errors resulting from subjectivity and the aging of the sample during analysis. In the process, metered amounts of one or more solvents are passed sequentially through a filter containing the sample under the direction of a microprocessor control apparatus. The mixture in the filter is agitated by ultrasonic cavitation for a timed period and the filtrate is collected. The filtrate of each solvent extraction is collected individually and the residue on the filter element is collected to complete the extraction process. 4 figs.

  7. Countercurrent Process for Lignin Separation from Biomass Matrix

    SciTech Connect (OSTI)

    Kiran Kadam; Ed Lehrburger

    2006-03-31T23:59:59.000Z

    The overall goal of the project was to test the concept of using a twin-screw extruder to conduct autohydrolysis pretreatment of wheat straw in countercurrent fashion, demonstrate in situ solid/liquid separation, and produce a low-lignin cellulose product using ethanol as an extractant. The resultant solid product is suitable for sugar production through enzymatic hydrolysis and for pulp applications. Pilot-scale equipment was used to successfully demonstrate the process both for sugar and pulp applications.

  8. Nitrogen Trifluoride-Based Fluoride- Volatility Separations Process: Initial Studies

    SciTech Connect (OSTI)

    McNamara, Bruce K.; Scheele, Randall D.; Casella, Andrew M.; Kozelisky, Anne E.

    2011-09-28T23:59:59.000Z

    This document describes the results of our investigations on the potential use of nitrogen trifluoride as the fluorinating and oxidizing agent in fluoride volatility-based used nuclear fuel reprocessing. The conceptual process uses differences in reaction temperatures between nitrogen trifluoride and fuel constituents that produce volatile fluorides to achieve separations and recover valuable constituents. We provide results from our thermodynamic evaluations, thermo-analytical experiments, kinetic models, and provide a preliminary process flowsheet. The evaluations found that nitrogen trifluoride can effectively produce volatile fluorides at different temperatures dependent on the fuel constituent.

  9. Formation of Light Isotopes by Protons and Deuterons of 3.65 GeV/nucleon on Separated Tin Isotopes

    E-Print Network [OSTI]

    A. R. Balabekyan; A. S. Danagulyan; J. R. Drnoyan; G. H. Hovhannisyan; J. Adam; V. G. Kalinnikov; M. I. Krivopustov; V. S. Pronskikh; V. I. Stegailov; A. A. Solnyshkin; P. Chaloun; V. M. Tsoupko-Sitnikov; S. G. Mashnik; K. K. Gudima

    2005-06-22T23:59:59.000Z

    We measure cross sections for residual nuclide formation in the mass range 6 tin isotopes (112-Sn, 118-Sn, 120-Sn, 124-Sn). The experimental data are compared with calculations by the codes FLUKA, LAHET, CEM03, and LAQGSM03. Scaling behavior is observed for the whole mass region of residual nuclei, showing a possible multifragmentation mechanism for the formation of light products (6 < A < 31). Our analysis of the isoscaling dependence also shows a possible contribution of multifragmentation to the production of heavier nuclides, in the mass region 39 < A < 81.

  10. Process for separation and preconcentration of radium from water

    DOE Patents [OSTI]

    Dietz, M.; Horwitz, E.P.; Chiarizia, R.; Bartsch, R.A.

    1999-01-26T23:59:59.000Z

    A process for preconcentrating and separating radium from a contaminated solution containing at least water and radium includes the steps of adding a quantity of a water-soluble macrocyclic polyether to the contaminated solution to form a combined solution. An acid is added to the combined solution to form an acidic combined solution having an [H{sup +}] concentration of about 0.5M. The acidic combined solution is contacted with a sulfonic acid-based strong acid cation exchange medium or a organophilic sulfonic acid medium having a plurality of binding sites thereon to bind the radium thereto and to form a radium-depleted solution. The radium-depleted solution is separated from the strong acid cation exchange medium or organophilic sulfonic acid medium. The radium remaining bound to the exchange medium or organophilic reagent is then stripped from the exchange medium or organophilic medium and the activity of the radium is measured. 24 figs.

  11. Process for separation and preconcentration of radium from water

    DOE Patents [OSTI]

    Dietz, Mark (Elmhurst, IL); Horwitz, E. Philip (Naperville, IL); Chiarizia, Renato (Elmhurst, IL); Bartsch, Richard A. (Lubbock, TX)

    1999-01-01T23:59:59.000Z

    A process for preconcentrating and separating radium from a contaminated solution containing at least water and radium includes the steps of adding a quantity of a water-soluble macrocyclic polyether to the contaminated solution to form a combined solution. An acid is added to the combined solution to form an acidic combined solution having an ›H.sup.+ ! concentration of about 0.5M. The acidic combined solution is contacted with a sulfonic acid-based strong acid cation exchange medium or a organophilic sulfonic acid medium having a plurality of binding sites thereon to bind the radium thereto and to form a radium-depleted solution. The radium-depleted solution is separated from the strong acid cation exchange medium or organophilic sulfonic acid medium. The radium remaining bound to the exchange medium or organophilic reagent is then stripped from the exchange medium or organophilic medium and the activity of the radium is measured.

  12. Combined heat and mass transfer device for improving separation process

    DOE Patents [OSTI]

    Tran, Thanh Nhon (Flossmoor, IL)

    1999-01-01T23:59:59.000Z

    A two-phase small channel heat exchange matrix simultaneously provides for heat transfer and mass transfer between the liquid and vapor phases of a multi-component mixture at a single, predetermined location within a separation column, significantly improving the thermodynamic efficiency of the separation process. The small channel heat exchange matrix is composed of a series of channels having a hydraulic diameter no greater than 5.0 millimeters for conducting a two-phase coolant. In operation, the matrix provides the liquid-vapor contacting surfaces within the separation column, such that heat and mass are transferred simultaneously between the liquid and vapor phases. The two-phase coolant allows for a uniform heat transfer coefficient to be maintained along the length of the channels and across the surface of the matrix. Preferably, a perforated, concave sheet connects each channel to an adjacent channel to facilitate the flow of the liquid and vapor phases within the column and to increase the liquid-vapor contacting surface area.

  13. Combined heat and mass transfer device for improving separation process

    DOE Patents [OSTI]

    Tran, T.N.

    1999-08-24T23:59:59.000Z

    A two-phase small channel heat exchange matrix simultaneously provides for heat transfer and mass transfer between the liquid and vapor phases of a multi-component mixture at a single, predetermined location within a separation column, significantly improving the thermodynamic efficiency of the separation process. The small channel heat exchange matrix is composed of a series of channels having a hydraulic diameter no greater than 5.0 millimeters for conducting a two-phase coolant. In operation, the matrix provides the liquid-vapor contacting surfaces within the separation column, such that heat and mass are transferred simultaneously between the liquid and vapor phases. The two-phase coolant allows for a uniform heat transfer coefficient to be maintained along the length of the channels and across the surface of the matrix. Preferably, a perforated, concave sheet connects each channel to an adjacent channel to facilitate the flow of the liquid and vapor phases within the column and to increase the liquid-vapor contacting surface area. 12 figs.

  14. Technetium and Iodine Separations in the UREX Process.

    SciTech Connect (OSTI)

    Schroeder, N. C. (Norman C.); Attrep, Moses; Marrero, T. (Thomas)

    2001-01-01T23:59:59.000Z

    The Accelerator Transmutation of Waste (ATW) program is being developed to determine the feasibility of separatin and transmutating the transactinides (Pu-Cm) and long-lived fission product (99Tc and 'I) from spent light water reactor (LWR) fuel. This approach would help with the disposal of spent commercial fuel. In addition, since the residual waste after ATW treatment will have much lower levels of long-lived species, this process may improve the performance and acceptability of long-term geologic disposal of nuclear waste. A roadmap for the Accelerator Transmutation of Waste (ATW) was submitted to Congress in 1999.' This document gave an overall view of the ATW concept and program. A subsequent document prepared by the Technical Working Group for ATW Separations Technologies and Waste Forms issued a second roadmap that dealt more specifically with the radionuclide separations and waste disposal needs for the ATW program.' This latter document discusses the UREX (Uranium Extraction) process. The latest iteration of the UREX flowsheet is shown in Figure le3T his flowsheet anticipates the co-extraction of technetium with uranium from dissolved LWR fuel by tributylphosphate (TBP) and their subsequent sequential bwk-extraction from the TBP stream.

  15. Process for separating carbon dioxide from flue gas using sweep-based membrane separation and absorption steps

    DOE Patents [OSTI]

    Wijmans, Johannes G.; Baker, Richard W.; Merkel, Timothy C.

    2012-08-21T23:59:59.000Z

    A gas separation process for treating flue gases from combustion processes, and combustion processes including such gas separation. The invention involves routing a first portion of the flue gas stream to be treated to an absorption-based carbon dioxide capture step, while simultaneously flowing a second portion of the flue gas across the feed side of a membrane, flowing a sweep gas stream, usually air, across the permeate side, then passing the permeate/sweep gas to the combustor.

  16. ISOTOPES

    E-Print Network [OSTI]

    Lederer, C. Michael

    2013-01-01T23:59:59.000Z

    the columns used to separate UF5, which had a separativeof uranium by dissociation of UF5, by multiple vibrational

  17. Addressing Energy Costs of Current Separation Processes with Advanced Materials and Large scale purification and separation processes transform low value resources into more

    E-Print Network [OSTI]

    Li, Mo

    Addressing Energy Costs of Current Separation Processes with Advanced Materials and Processes Large scale purification and separation processes transform low value resources into more useful fuels, basic chemicals, food and clean water; however, they also consume considerable energy. With growing global

  18. Candidate processes for diluting the {sup 235}U isotope in weapons-capable highly enriched uranium

    SciTech Connect (OSTI)

    Snider, J.D.

    1996-02-01T23:59:59.000Z

    The United States Department of Energy (DOE) is evaluating options for rendering its surplus inventories of highly enriched uranium (HEU) incapable of being used to produce nuclear weapons. Weapons-capable HEU was earlier produced by enriching uranium in the fissile {sup 235}U isotope from its natural occurring 0.71 percent isotopic concentration to at least 20 percent isotopic concentration. Now, by diluting its concentration of the fissile {sup 235}U isotope in a uranium blending process, the weapons capability of HEU can be eliminated in a manner that is reversible only through isotope enrichment, and therefore, highly resistant to proliferation. To the extent that can be economically and technically justified, the down-blended uranium product will be made suitable for use as commercial reactor fuel. Such down-blended uranium product can also be disposed of as waste if chemical or isotopic impurities preclude its use as reactor fuel.

  19. Method and apparatus for separation of heavy and tritiated water

    DOE Patents [OSTI]

    Lee, Myung W. (late of North Augusta, SC)

    2001-01-01T23:59:59.000Z

    The present invention is a bi-thermal membrane process for separating and recovering hydrogen isotopes from a fluid containing hydrogen isotopes, such as water and hydrogen gas. The process in accordance with the present invention provides counter-current cold and hot streams of the fluid separated with a thermally insulating and chemically transparent proton exchange membrane (PEM). The two streams exchange hydrogen isotopes through the membrane: the heavier isotopes migrate into the cold stream, while the lighter isotopes migrate into the hot stream. The heavy and light isotopes are continuously withdrawn from the cold and hot streams respectively.

  20. Continuous production of tritium in an isotope-production reactor with a separate circulation system

    DOE Patents [OSTI]

    Cawley, W.E.; Omberg, R.P.

    1982-08-19T23:59:59.000Z

    A method is described for producing tritium in a fast breeder reactor cooled with liquid metal. Lithium is allowed to flow through the reactor in separate loops in order to facilitate the production and removal of tritium.

  1. Process for the recovery and separation of plastics

    DOE Patents [OSTI]

    Jody, Bassam J.; Daniels, Edward J.; Pomykala Jr., Joseph A.

    2003-07-29T23:59:59.000Z

    A method of separating a portion of acrylonitrile-butadiene-styrene (ABS) from a mixture containing ABS and for separating a portion of ABS and polycarbonate (PC) from a mixture of plastics containing ABS and PC is disclosed. The method includes shredding and/or granulating the mixture of plastics containing ABS and PC to provide a selected particle size; sequentially dispersing the shredded mixture of plastics in a series aqueous solutions having different specific gravities and separating the floating fraction until the desired separation is obtained. Surface tension and pH are also variable to be controlled.

  2. Isotopes

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645U.S. DOEThe Bonneville PowerCherries 82981-1cnHigh SchoolIn12 Investigation Peer ReviewIronNuclear Physics » Isotopes

  3. Recent developments of the ion sources at Tri University Meson Factory/Isotope Separator and ACcelerator Facility

    SciTech Connect (OSTI)

    Bricault, P. G.; Ames, F.; Dombsky, M.; Labrecque, F.; Lassen, J.; Mjos, A.; Minor, G. [TRIUMF, 4004 Wesbrook Mall, Vancouver, British Columbia V6T 2A3 (Canada); Tigelhoefer, A. [TRIUMF, 4004 Wesbrook Mall, Vancouver, British Columbia V6T 2A3 (Canada); Department Of Physics, University of Manitoba, Winnipeg, Manitoba R3T 2N2 (Canada)

    2012-02-15T23:59:59.000Z

    This paper describes the recent progresses concerning the on-line ion source at the Tri University Meson Factory/Isotope Separator and ACcelerator (TRIUMF/ISAC) Radioactive Ion-Beam Facility; description of the new design of the surface-ion-source for improved stability of the beam intensity, description of the transport path to the east target station at ISAC, description of the new brazing techniques that solved recurrent problems with water leaks on the target/ion source assembly in the vacuum system, finally, recent developments concerning the Forced Electron Beam Induced Arc Discharge (FEBIAD) ion source are reported. In particular, a study on the effect of the plasma chamber volume on the ionization efficiency was completed.

  4. Characterization of Diesel Fuel by Chemical Separation Combined with Capillary Gas Chromatography (GC) Isotope Ratio Mass Spectrometry (IRMS)

    SciTech Connect (OSTI)

    Harvey, Scott D.; Jarman, Kristin H.; Moran, James J.; Sorensen, Christina M.; Wright, Bob W.

    2011-09-15T23:59:59.000Z

    The purpose of this study was to perform a preliminary investigation of compound-specific isotope analysis (CSIA) of diesel fuels to evaluate whether the technique could distinguish between the diesel samples from different sources/locations. The ability to differentiate or correlate diesel samples could be valuable for detecting fuel tax evasion schemes. Two fractionation techniques were used to isolate the n-alkanes from the fuel. Both ?13C and ?D values for the n-alkanes were then determined by CSIA in each sample. Plots of ?D versus ?13C with sample n-alkane points connected in order of increasing carbon number gave well separated clusters with characteristic shapes for each sample. Principal components analysis (PCA) with ?13C, ?D, or combined ?13C and ?D data on the yielded scores plots that could clearly differentiate the samples, thereby demonstrating the potential of this approach for fingerprinting fuel samples using the ?13C and ?D values.

  5. Measurement of isotope separation factors in the palladium-hydrogen system using a thermistor technique

    SciTech Connect (OSTI)

    Ortiz, T.M.

    1998-05-01T23:59:59.000Z

    The range of available data on separation factors in the palladium-hydrogen/deuterium system has been extended. A matched pair of glass-coated bead thermistors was used to measure gas phase compositions. The compositions of the input gas--assumed also to be the solid phase composition--were measured independently be mass spectrometry as being within 0.5 mole% of the values used to calibrate the thermistors. This assumption is based on the fact that > 99% of the input gas is absorbed into the solid. Separation factors were measured for 175 K {le} T {le} 389 K and for 0.195 {le} x{sub H} {le} 0.785.

  6. On the Design of Crystallization-Based Separation Processes: Review and Extension

    E-Print Network [OSTI]

    Grossmann, Ignacio E.

    flow sheets for separations based on fractional crystallization. A series of rules are derived that may Keywords: fractional crystallization, process design, process synthesis Introduction Crystallization. In spite of the popularity of this operation, exceeded in scope only by distillation processes

  7. Isotope separation of {sup 17}O by photodissociation of ozone with near-infrared laser irradiation

    SciTech Connect (OSTI)

    Hayashida, Shigeru; Kambe, Takashi; Sato, Tetsuya; Igarashi, Takehiro [Tsukuba Laboratories, Taiyo Nippon Sanso Corporation, 10 Okubo Tsukuba-shi, Ibaraki 300-2611 (Japan); Kuze, Hiroaki [Center for Environmental Remote Sensing, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba, 263-8522 (Japan)

    2012-04-01T23:59:59.000Z

    Oxygen-17 is a stable oxygen isotope useful for various diagnostics in both engineering and medical applications. Enrichment of {sup 17}O, however, has been very costly due to the lack of appropriate methods that enable efficient production of {sup 17}O on an industrial level. In this paper, we report the first {sup 17}O-selective photodissociation of ozone at a relatively high pressure, which has been achieved by irradiating a gas mixture of 10 vol% O{sub 3}-90 vol% CF{sub 4} with narrowband laser. The experiment was conducted on a pilot-plant scale. A total laser power of 1.6 W was generated by external-cavity diode lasers with all the laser wavelengths fixed at the peak of an absorption line of {sup 16}O{sup 16}O{sup 17}O around 1 {mu}m. The beams were introduced into a 25 -m long photoreaction cell under the sealed-off condition with a total pressure of 20 kPa. Lower cell temperature reduced the background decomposition of ozone, and at the temperature of 158 K, an {sup 17}O enrichment factor of 2.2 was attained.

  8. Carbon Dioxide Sequestration Industrial-scale processes are available for separating carbon dioxide from the post-

    E-Print Network [OSTI]

    Carbon Dioxide Sequestration Industrial-scale processes are available for separating carbon dioxide dioxide separation and sequestration because the lower cost of carbon dioxide separation from for injection of carbon dioxide into oil or gas-bearing formations. An advantage of sequestration involving

  9. Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Portsmouth Gaseous Diffusion Plant site

    SciTech Connect (OSTI)

    Marmer, G.J.; Dunn, C.P.; Filley, T.H.; Moeller, K.L.; Pfingston, J.M.; Policastro, A.J.; Cleland, J.H.

    1991-09-01T23:59:59.000Z

    Uranium enrichment in the United States has utilized a diffusion process to preferentially enrich the U-235 isotope in the uranium product. In the 1970s, the US Department of Energy (DOE) began investigating more efficient and cost-effective enrichment technologies. In January 1990, the Secretary of Energy approved a plan for the demonstration and deployment of the Uranium Atomic Vapor Laser isotope Separation (U-AVLIS) technology with the near-term goal to provide the necessary information to make a deployment decision by November 1992. Initial facility operation is anticipated for 1999. A programmatic document for use in screening DOE sites to locate a U-AVLIS production plant was developed and implemented in two parts. The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. The final evaluation, which included sensitivity studies, identified the Oak Ridge Gaseous Diffusion Plant (ORGDP) site, the Paducah Gaseous Diffusion Plant (PGDP) site, and the Portsmouth Gaseous Diffusion Plant (PORTS) site as having significant advantages over the other sites considered. This environmental site description (ESD) provides a detailed description of the PORTS site and vicinity suitable for use in an environmental impact statement (EIS). This report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during site visits. The organization of the ESD is as follows. Topics addressed in Sec. 2 include a general site description and the disciplines of geology, water resources, biotic resources, air resources, noise, cultural resources, land use. Socioeconomics, and waste management. Identification of any additional data that would be required for an EIS is presented in Sec. 3.

  10. Isotopic Analysis At Separation Creek Area (Van Soest, Et Al., 2002) | Open

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are8COaBulkTransmissionSitingProcess.pdfGetecGtelInterias Solar Energy JumpIremNot2007) | Open EnergyOpenEnergy

  11. The Multi-Isotope Process (MIP) Monitor Project: FY13 Final Report

    SciTech Connect (OSTI)

    Meier, David E.; Coble, Jamie B.; Jordan, David V.; Mcdonald, Luther W.; Forrester, Joel B.; Schwantes, Jon M.; Unlu, Kenan; Landsberger, Sheldon; Bender, Sarah; Dayman, Kenneth J.; Reilly, Dallas D.

    2013-09-01T23:59:59.000Z

    The Multi-Isotope Process (MIP) Monitor provides an efficient approach to monitoring the process conditions in reprocessing facilities in support of the goal of “… (minimization of) the risks of nuclear proliferation and terrorism.” The MIP Monitor measures the distribution of the radioactive isotopes in product and waste streams of a nuclear reprocessing facility. These isotopes are monitored online by gamma spectrometry and compared, in near-real-time, to spectral patterns representing “normal” process conditions using multivariate analysis and pattern recognition algorithms. The combination of multivariate analysis and gamma spectroscopy allows us to detect small changes in the gamma spectrum, which may indicate changes in process conditions. By targeting multiple gamma-emitting indicator isotopes, the MIP Monitor approach is compatible with the use of small, portable, relatively high-resolution gamma detectors that may be easily deployed throughout an existing facility. The automated multivariate analysis can provide a level of data obscurity, giving a built-in information barrier to protect sensitive or proprietary operational data. Proof-of-concept simulations and experiments have been performed in previous years to demonstrate the validity of this tool in a laboratory setting for systems representing aqueous reprocessing facilities. However, pyroprocessing is emerging as an alternative to aqueous reprocessing techniques.

  12. Nucleon-induced fission cross-sections of tantalum and separated tungsten isotopes and "compound nucleus" effect in intermediate energy region

    E-Print Network [OSTI]

    A. N. Smirnov; O. I. Batenkov; V. P. Eismont; N. P. Filatov; J. Blomgren; H. Conde; A. V. Prokofiev; S. G. Mashnik

    2007-05-21T23:59:59.000Z

    Neutron- and proton-induced fission cross-sections of separated isotopes of tungsten (182W, 183W, 184W, and 186W) and 181Ta relative to 209Bi have been measured in the incident nucleon energy region 50 - 200 MeV using fission chambers based on thin-film breakdown counters (TFBC) using quasi-monoenergetic neutrons from the 7Li(p,n) reaction and at the proton beams of The Svedberg Laboratory (TSL), Uppsala University (Uppsala, Sweden). The results are compared with predictions by the CEM03.01 event generator, as well as with the recent data for nuclei in the lead-bismuth region. The effect of "compound nucleus" in the intermediate energy region is discussed, displaying in exponential dependence of nucleon-induced fission cross-sections on the parameter Z^2/A of the composite system (projectile+target nucleus), and in other characteristics of the fission process for which parameter Z^2/A plays a role similar to the one of the usual liquid-drop parameter Z^2/A of compound nuclei.

  13. Functionalized sorbent for chemical separations and sequential forming process

    DOE Patents [OSTI]

    Fryxell, Glen E. (Kennewick, WA); Zemanian, Thomas S. (Richland, WA)

    2012-03-20T23:59:59.000Z

    A highly functionalized sorbent and sequential process for making are disclosed. The sorbent includes organic short-length amino silanes and organic oligomeric polyfunctional amino silanes that are dispersed within pores of a porous support that form a 3-dimensional structure containing highly functionalized active binding sites for sorption of analytes.

  14. Process to separate transuranic elements from nuclear waste

    DOE Patents [OSTI]

    Johnson, Terry R. (Wheaton, IL); Ackerman, John P. (Downers Grove, IL); Tomczuk, Zygmunt (Orland Park, IL); Fischer, Donald F. (Glen Ellyn, IL)

    1989-01-01T23:59:59.000Z

    A process for removing transuranic elements from a waste chloride electrolytic salt containing transuranic elements in addition to rare earth and other fission product elements so the salt waste may be disposed of more easily and the valuable transuranic elements may be recovered for reuse. The salt is contacted with a cadmium-uranium alloy which selectively extracts the transuranic elements from the salt. The waste salt is generated during the reprocessing of nuclear fuel associated with the Integral Fast Reactor (IFR).

  15. Process to separate transuranic elements from nuclear waste

    DOE Patents [OSTI]

    Johnson, T.R.; Ackerman, J.P.; Tomczuk, Z.; Fischer, D.F.

    1988-07-12T23:59:59.000Z

    A process for removing transuranic elements from a waste chloride electrolytic salt containing transuranic elements in addition to rare earth and other fission product elements so the salt waste may be disposed of more easily and the valuable transuranic elements may be recovered for reuse. The salt is contacted with a cadmium-uranium alloy which selectively extracts the transuranic elements from the salt. The waste salt is generated during the reprocessing of nuclear fuel associated with the Integral Fast Reactor (IFR). 2 figs.

  16. Process to separate transuranic elements from nuclear waste

    DOE Patents [OSTI]

    Johnson, T.R.; Ackerman, J.P.; Tomczuk, Z.; Fischer, D.F.

    1989-03-21T23:59:59.000Z

    A process is described for removing transuranic elements from a waste chloride electrolytic salt containing transuranic elements in addition to rare earth and other fission product elements so the salt waste may be disposed of more easily and the valuable transuranic elements may be recovered for reuse. The salt is contacted with a cadmium-uranium alloy which selectively extracts the transuranic elements from the salt. The waste salt is generated during the reprocessing of nuclear fuel associated with the Integral Fast Reactor (IFR). 2 figs.

  17. Process for separating an ethylenically unsaturated hydrocarbon from a hydrocarbon mixture

    SciTech Connect (OSTI)

    vanEijl, A.T.

    1986-06-24T23:59:59.000Z

    A process is described for separating an ethylenically unsaturated hydrocarbon from a hydrocarbon mixture characterized by: (a) distilling a hydrocarbon mixture containing the unsaturated hydrocarbon with an N-(aminoalkyl) piperazine; and (b) separating the amine/hydrocarbon mixture into at least two factions, one of which contains the amine and the unsaturated hydrocarbon.

  18. Separation of Zirconium from Uranium in U-Zr Alloys Using a Chlorination Process

    E-Print Network [OSTI]

    Parkison, Adam J

    2013-06-04T23:59:59.000Z

    The fundamental behavior underpinning a new processing concept was demonstrated which is capable of separating uranium from zirconium in U-Zr alloys through the formation and selective volatilization of their respective chlorides. Bench...

  19. Electrostatic coalescence of used automotive crankcase oil as an alternative to other separation processes 

    E-Print Network [OSTI]

    Dixon, John Leslie

    1998-01-01T23:59:59.000Z

    This thesis presents an initial investigation of using electrostatic coalescence as an alternative to conventional separation processes to purify used automotive crankcase oil. Specific emphasis of this study was the feasibility of this approach...

  20. Separation of Zirconium from Uranium in U-Zr Alloys Using a Chlorination Process 

    E-Print Network [OSTI]

    Parkison, Adam J

    2013-06-04T23:59:59.000Z

    The fundamental behavior underpinning a new processing concept was demonstrated which is capable of separating uranium from zirconium in U-Zr alloys through the formation and selective volatilization of their respective chlorides. Bench...

  1. A process for separation by semi-continuous counter-current crystallization

    E-Print Network [OSTI]

    Aumock, Nathan M. (Nathan Micheal)

    2011-01-01T23:59:59.000Z

    A process is proposed to perform separations via crystallization by using multiple tanks and constraining crystal growth to solid surfaces. Multiple tanks allow multiple recrystallizations to improve product purity and to ...

  2. Process for the production of ultrahigh purity silane with recycle from separation columns

    DOE Patents [OSTI]

    Coleman, Larry M. (Tonawanda, NY)

    1982-07-20T23:59:59.000Z

    Tri- and dichlorosilanes formed by hydrogenation in the course of the reaction of metallurgical silicon, hydrogen and recycle silicon tetrachloride are employed as feed into a separation column arrangement of sequential separation columns and redistribution reactors which processes the feed into ultrahigh purity silane and recycle silicon tetrachloride. A slip stream is removed from the bottom of two sequential columns and added to the recycle silicon tetrachloride process stream causing impurities in the slip streams to be subjected to reactions in the hydrogenation step whereby waste materials can be formed and readily separated.

  3. The Multi-Isotope Process (MIP) Monitor Project: FY12 Progress and Accomplishments

    SciTech Connect (OSTI)

    Coble, Jamie B.; Orton, Christopher R.; Jordan, David V.; Schwantes, Jon M.; Bender, Sarah; Dayman, Kenneth J.; Unlu, Kenan; Landsberger, Sheldon

    2012-09-27T23:59:59.000Z

    The Multi-Isotope Process (MIP) Monitor, being developed at Pacific Northwest National Laboratory (PNNL), provides an efficient approach to monitoring the process conditions in reprocessing facilities in support of the goal of "...(minimization of) the risks of nuclear proliferation and terrorism." The MIP Monitor measures distributions of a suite of indicator (radioactive) isotopes present within product and waste streams of a nuclear reprocessing facility. These indicator isotopes are monitored on-line by gamma spectrometry and compared, in near-real-time, to spectral patterns representing "normal" process conditions using multivariate pattern recognition software. The monitor utilizes this multivariate analysis and gamma spectroscopy of reprocessing streams to detect small changes in the gamma spectrum, which may indicate changes in process conditions. Multivariate analysis methods common in chemometrics, such as principal component analysis (PCA) and partial least squares regression (PLS), act as pattern recognition techniques, which can detect small deviations from the expected, nominal condition. By targeting multiple gamma-emitting indicator isotopes, the MIP Monitor approach is compatible with the use of small, portable, relatively high-resolution gamma detectors that may be easily deployed throughout an existing facility. The automated multivariate analysis can provide a level of data obscurity, giving a built-in information barrier to protect sensitive or proprietary operational data. Proof-of-concept simulations and experiments have been performed in previous years to demonstrate the validity of this tool in a laboratory setting. Development of the MIP Monitor approach continues to evaluate the efficacy of the monitor for automated, real-time or near-real-time application. This report details follow-on research and development efforts sponsored by the U.S. Department of Energy Fuel Cycle Research and Development related to the MIP Monitor for fiscal year 2012 (FY12).

  4. Process for preparing a chemical compound enriched in isotope content. [nitrogen 15-enriched nitric acid

    DOE Patents [OSTI]

    Michaels, E.D.

    1981-02-25T23:59:59.000Z

    A process to prepare a chemical enriched in isotope content includes: a chemical exchange reaction between a first and second compound which yields an isotopically enriched first compound and an isotopically depleted second compound; the removal of a portion of the first compound as product and the removal of a portion of the second compound as spent material; the conversion of the remainder of the first compound to the second compound for reflux at the product end of the chemical exchange reaction region; the conversion of the remainder of the second compound to the first compound for reflux at the spent material end of the chemical exchange region; and the cycling of the additional chemicals produced by one conversion reaction to the other conversion reaction, for consumption therein. One of the conversion reactions is an oxidation reaction, and the energy that it yields is used to drive the other conversion reaction, a reduction. The reduction reaction is carried out in a solid polymer electrolyte electrolytic reactor. The overall process is energy efficient and yields no waste by-products. A particular embodiment of the process in the production of nitrogen-15-enriched nitric acid.

  5. Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Oak Ridge Gaseous Diffusion Plant Site

    SciTech Connect (OSTI)

    Not Available

    1991-09-01T23:59:59.000Z

    In January 1990, the Secretary of Energy approved a plan for the demonstration and deployment of the Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) technology, with the near-term goal to provide the necessary information to make a deployment decision by November 1992. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. A programmatic document for use in screening DOE sites to locate the U-AVLIS production plant was developed and implemented in two parts (Wolsko et al. 1991). The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were then subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the ORGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. The organization of the ESD is as follows. Topics addressed in Sec. 2 include a general site description and the disciplines of geology, water resources, biotic resources, air resources, noise, cultural resources, land use, socioeconomics, and waste management. Identification of any additional data that would be required for an EIS is presented in Sec. 3. Following the site description and additional data requirements, Sec. 4 provides a short, qualitative assessment of potential environmental issues. 37 refs., 20 figs., 18 tabs.

  6. Process for coal liquefaction by separation of entrained gases from slurry exiting staged dissolvers

    DOE Patents [OSTI]

    Givens, Edwin N. (Bethlehem, PA); Ying, David H. S. (Macungie, PA)

    1983-01-01T23:59:59.000Z

    There is described an improved liquefaction process by which coal is converted to a low ash and low sulfur carbonaceous material that can be used as a fuel in an environmentally acceptable manner without costly gas scrubbing equipment. In the process, coal is slurried with a solvent, passed through a preheater and at least two dissolvers in series in the presence of hydrogen-rich gases at elevated temperatures and pressures. Solids, including mineral ash and unconverted coal macerals are separated from the condensed dissolver effluent. In accordance with the improved process, fresh hydrogen is fed to each dissolver and the entrained gas from each dissolver is separated from the slurry phase and removed from the reactor system before the condensed phase is passed to the next dissolver in the series. In accordance with another process, the feeds to the dissolvers are such that the top of each downstream dissolver is used as a gas-liquid separator.

  7. CORROSION ISSUES ASSOCIATED WITH AUSTENITIC STAINLESS STEEL COMPONENTS USED IN NUCLEAR MATERIALS EXTRACTION AND SEPARATION PROCESSES

    SciTech Connect (OSTI)

    Mickalonis, J.; Louthan, M.; Sindelar, R.

    2012-12-17T23:59:59.000Z

    This paper illustrated the magnitude of the systems, structures and components used at the Savannah River Site for nuclear materials extraction and separation processes. Corrosion issues, including stress corrosion cracking, pitting, crevice corrosion and other corrosion induced degradation processes are discussed and corrosion mitigation strategies such as a chloride exclusion program and corrosion release testing are also discussed.

  8. Laser Isotope Enrichment for Medical and Industrial Applications

    SciTech Connect (OSTI)

    Leonard Bond

    2006-07-01T23:59:59.000Z

    Laser Isotope Enrichment for Medical and Industrial Applications by Jeff Eerkens (University of Missouri), Jay Kunze (Idaho State University), and Leonard Bond (Idaho National Laboratory) The principal isotope enrichment business in the world is the enrichment of uranium for commercial power reactor fuels. However, there are a number of other needs for separated isotopes. Some examples are: 1) Pure isotopic targets for irradiation to produce medical radioisotopes. 2) Pure isotopes for semiconductors. 3) Low neutron capture isotopes for various uses in nuclear reactors. 4) Isotopes for industrial tracer/identification applications. Examples of interest to medicine are targets to produce radio-isotopes such as S-33, Mo-98, Mo-100, W-186, Sn-112; while for MRI diagnostics, the non-radioactive Xe-129 isotope is wanted. For super-semiconductor applications some desired industrial isotopes are Si-28, Ga-69, Ge-74, Se-80, Te-128, etc. An example of a low cross section isotope for use in reactors is Zn-68 as a corrosion inhibitor material in nuclear reactor primary systems. Neutron activation of Ar isotopes is of interest in industrial tracer and diagnostic applications (e.g. oil-logging). . In the past few years there has been a sufficient supply of isotopes in common demand, because of huge Russian stockpiles produced with old electromagnetic and centrifuge separators previously used for uranium enrichment. Production of specialized isotopes in the USA has been largely accomplished using old ”calutrons” (electromagnetic separators) at Oak Ridge National Laboratory. These methods of separating isotopes are rather energy inefficient. Use of lasers for isotope separation has been considered for many decades. None of the proposed methods have attained sufficient proof of principal status to be economically attractive to pursue commercially. Some of the authors have succeeded in separating sulfur isotopes using a rather new and different method, known as condensation repression. In this scheme a gas, of the selected isotopes for enrichment, is irradiated with a laser at a particular wavelength that would excite only one of the isotopes. The entire gas is subject to low temperatures sufficient to cause condensation on a cold surface. Those molecules in the gas that the laser excited are not as likely to condense as are the unexcited molecules. Hence the gas drawn out of the system will be enriched in the isotope that was excited by the laser. We have evaluated the relative energy required in this process if applied on a commercial scale. We estimate the energy required for laser isotope enrichment is about 20% of that required in centrifuge separations, and 2% of that required by use of "calutrons".

  9. Membrane loop process for separating carbon dioxide for use in gaseous form from flue gas

    DOE Patents [OSTI]

    Wijmans, Johannes G; Baker, Richard W; Merkel, Timothy C

    2014-10-07T23:59:59.000Z

    The invention is a process involving membrane-based gas separation for separating and recovering carbon dioxide emissions from combustion processes in partially concentrated form, and then transporting the carbon dioxide and using or storing it in a confined manner without concentrating it to high purity. The process of the invention involves building up the concentration of carbon dioxide in a gas flow loop between the combustion step and a membrane separation step. A portion of the carbon dioxide-enriched gas can then be withdrawn from this loop and transported, without the need to liquefy the gas or otherwise create a high-purity stream, to a destination where it is used or confined, preferably in an environmentally benign manner.

  10. Extensive separations (CLEAN) processing strategy compared to TRUEX strategy and sludge wash ion exchange

    SciTech Connect (OSTI)

    Knutson, B.J.; Jansen, G.; Zimmerman, B.D.; Seeman, S.E. [Westinghouse Hanford Co., Richland, WA (United States); Lauerhass, L.; Hoza, M. [Pacific Northwest Lab., Richland, WA (United States)

    1994-08-01T23:59:59.000Z

    Numerous pretreatment flowsheets have been proposed for processing the radioactive wastes in Hanford`s 177 underground storage tanks. The CLEAN Option is examined along with two other flowsheet alternatives to quantify the trade-off of greater capital equipment and operating costs for aggressive separations with the reduced waste disposal costs and decreased environmental/health risks. The effect on the volume of HLW glass product and radiotoxicity of the LLW glass or grout product is predicted with current assumptions about waste characteristics and separations processes using a mass balance model. The prediction is made on three principal processing options: washing of tank wastes with removal of cesium and technetium from the supernatant, with washed solids routed directly to the glass (referred to as the Sludge Wash C processing strategy); the previous steps plus dissolution of the solids and removal of transuranic (TRU) elements, uranium, and strontium using solvent extraction processes (referred to as the Transuranic Extraction Option C (TRUEX-C) processing strategy); and an aggressive yet feasible processing strategy for separating the waste components to meet several main goals or objectives (referred to as the CLEAN Option processing strategy), such as the LLW is required to meet the US Nuclear Regulatory Commission Class A limits; concentrations of technetium, iodine, and uranium are reduced as low as reasonably achievable; and HLW will be contained within 1,000 borosilicate glass canisters that meet current Hanford Waste Vitrification Plant glass specifications.

  11. Apparatus and process for the separation of gases using supersonic expansion and oblique wave compression

    DOE Patents [OSTI]

    VanOsdol, John G.

    2014-07-08T23:59:59.000Z

    The disclosure provides an apparatus and method for gas separation through the supersonic expansion and subsequent deceleration of a gaseous stream. The gaseous constituent changes phase from the gaseous state by desublimation or condensation during the acceleration producing a collectible constituent, and an oblique shock diffuser decelerates the gaseous stream to a subsonic velocity while maintain the collectible constituent in the non-gaseous state. Following deceleration, the carrier gas and the collectible constituent at the subsonic velocity are separated by a separation means, such as a centrifugal, electrostatic, or impingement separator. In an embodiment, the gaseous stream issues from a combustion process and is comprised of N.sub.2 and CO.sub.2.

  12. Apparatus and process for the refrigeration, liquefaction and separation of gases with varying levels of purity

    DOE Patents [OSTI]

    Bingham, Dennis N. (Idaho Falls, ID); Wilding, Bruce M. (Idaho Falls, ID); McKellar, Michael G. (Idaho Falls, ID)

    2000-01-01T23:59:59.000Z

    A process for the separation and liquefaction of component gasses from a pressurized mix gas stream is disclosed. The process involves cooling the pressurized mixed gas stream in a heat exchanger so as to condense one or more of the gas components having the highest condensation point; separating the condensed components from the remaining mixed gas stream in a gas-liquid separator; cooling the separated condensed component stream by passing it through an expander; and passing the cooled component stream back through the heat exchanger such that the cooled component stream functions as the refrigerant for the heat exchanger. The cycle is then repeated for the remaining mixed gas stream so as to draw off the next component gas and further cool the remaining mixed gas stream. The process continues until all of the component gases are separated from the desired gas stream. The final gas stream is then passed through a final heat exchanger and expander. The expander decreases the pressure on the gas stream, thereby cooling the stream and causing a portion of the gas stream to liquify within a tank. The portion of the gas which is not liquefied is passed back through each of the heat exchanges where it functions as a refrigerant.

  13. Apparatus and process for the refrigeration, liquefaction and separation of gases with varying levels of purity

    DOE Patents [OSTI]

    Bingham, Dennis N. (Idaho Falls, ID); Wilding, Bruce M. (Idaho Falls, ID); McKellar, Michael G. (Idaho Falls, ID)

    2002-01-01T23:59:59.000Z

    A process for the separation and liquefaction of component gasses from a pressurized mix gas stream is disclosed. The process involves cooling the pressurized mixed gas stream in a heat exchanger so as to condensing one or more of the gas components having the highest condensation point; separating the condensed components from the remaining mixed gas stream in a gas-liquid separator; cooling the separated condensed component stream by passing it through an expander; and passing the cooled component stream back through the heat exchanger such that the cooled component stream functions as the refrigerant for the heat exchanger. The cycle is then repeated for the remaining mixed gas stream so as to draw off the next component gas and further cool the remaining mixed gas stream. The process continues until all of the component gases are separated from the desired gas stream. The final gas stream is then passed through a final heat exchanger and expander. The expander decreases the pressure on the gas stream, thereby cooling the stream and causing a portion of the gas stream to liquify within a tank. The portion of the gas which is hot liquefied is passed back through each of the heat exchanges where it functions as a refrigerant.

  14. Method for separating water soluble organics from a process stream by aqueous biphasic extraction

    DOE Patents [OSTI]

    Chaiko, David J. (Naperville, IL); Mego, William A. (Naperville, IL)

    1999-01-01T23:59:59.000Z

    A method for separating water-miscible organic species from a process stream by aqueous biphasic extraction is provided. An aqueous biphase system is generated by contacting a process stream comprised of water, salt, and organic species with an aqueous polymer solution. The organic species transfer from the salt-rich phase to the polymer-rich phase, and the phases are separated. Next, the polymer is recovered from the loaded polymer phase by selectively extracting the polymer into an organic phase at an elevated temperature, while the organic species remain in a substantially salt-free aqueous solution. Alternatively, the polymer is recovered from the loaded polymer by a temperature induced phase separation (cloud point extraction), whereby the polymer and the organic species separate into two distinct solutions. The method for separating water-miscible organic species is applicable to the treatment of industrial wastewater streams, including the extraction and recovery of complexed metal ions from salt solutions, organic contaminants from mineral processing streams, and colorants from spent dye baths.

  15. Use of Separator with Regular Granular Filling in Extraction Processes - 12209

    SciTech Connect (OSTI)

    Volk, Vladimir; Veselov, Sergey; Zherebtsov, Alexander [Joint Stock Company 'A.A. Bochvar High-Technology Scientific Research Institute of Inorganic Materials' (VNIINM), Rogova st., 5A (Russian Federation)

    2012-07-01T23:59:59.000Z

    The separator with a regular granular filling has been developed to be used for the operations of the removal of carbon-black impurities from the aqueous flow; the intra-cycle regeneration of back-extractants; and the concentrating back-extraction of plutonium in the extraction SNF reprocessing technology. The process conditions for those operations have been experimentally tested using this separator. Thus, the separator for operations of concentrating reextraction of plutonium and regeneration recycling extractant allows to: - derive plutonium from the organic stream into an extremely concentrated form, reducing the amount of liquid radioactive waste (raffinate, decantate) plutonium branches to a minimum; - controlling the processes of concentration of uranium and plutonium, get uranium-plutonium product with required concentration and the amount of metal with required ratio; - eliminate contamination of the emulsion flows; - simplify the purification of uranium from the extract plutonium; - test results showed that when working on a solution 'hydrazine-DTPA' in the separator it is achieved the extraction of plutonium re-extract - 82% TC - at 56-65%. With the transition to the reextraction by solution 'U (IV)-hydrazine', of plutonium into re-extract increases to 95%, technetium - up to 83%; - regenerate the extractant recycling minimizing the amount of liquid radioactive waste generated as a technology used as well as alternative 'salt-free' systems; - it is found that the regeneration of the extractant solution of soda and EDA in the separator at a load of 3.2 m{sup 3} / (m{sup 2}.h) it can be achieved almost complete phase separation. Residual carryover of 0,005-0,006% emulsion is on the verge of analytical detection. - It is shown that in the depth of separation phase a separation of the extractant regeneration of quality superior is more than 5-7 times to the extraction. (authors)

  16. A Framework for Synthesizing the Optimal Separation Process of Azeotropic Mixtures

    E-Print Network [OSTI]

    Grossmann, Ignacio E.

    is separation feasibility. Products of columns are restricted within so-called distillation regions1 expands the feasible area. Moreover, detailed design parameters such as number of stages and reflux ratio of the process, and are able to be used as heuristic methods to guide the design of ternary or quaternary systems

  17. Frishkoff, Schneider & Tucker ONR Grantee Meeting 2005 1 EEG/ERP Control Process Separation

    E-Print Network [OSTI]

    Frishkoff, Schneider & Tucker ONR Grantee Meeting 2005 1 EEG/ERP Control Process Separation Gwen A.8 DLPFC %BOLD -0.2 1.2 PC Electrical Geodesics, Inc. #12;Frishkoff, Schneider & Tucker ONR Grantee Meeting & Tucker ONR Grantee Meeting 2005 3 Geodesic Sensor Net (Electrical Geodesics, Inc.) 128-channel 256

  18. A State-Of-The-Art Review of Low Energy Separation Processes

    E-Print Network [OSTI]

    Humphrey, J. L.; Fair, J. R.

    1983-01-01T23:59:59.000Z

    . Conclu sions are drawn on the merits of each type of separation process. INTRODUCTION The total energy consumed by the chemical and petroleum refining industries in converting feedstocks to p~oducts is equivalent to approxi mately 2.9 X 10 h bpd...

  19. Energy minimization of separation processes using conventional/membrane hybrid systems

    SciTech Connect (OSTI)

    Gottschlich, D.E.; Roberts, D.L. (SRI International, Menlo Park, CA (USA))

    1990-09-28T23:59:59.000Z

    The purpose of this study was to identify the general principles governing the choice of hybrid separation systems over straight membrane or straight nonmembrane systems and to do so by examining practical applications (process design and economics). Our focus was to examine the energy consumption characteristics and overall cost factors of the membrane and nonmembrane technologies that cause hybrid systems to be preferred over nonhybrid systems. We evaluated four cases studies, chosen on the basis of likelihood of commercial viability of a hybrid system and magnitude of energy savings: (1) propane/propylene separation; (2) removal of nitrogen from natural gas; (3) concentration of Kraft black liquor; and (4)solvent deasphalting. For propane/propylene splitting, the membrane proved to be superior to distillation in both thermodynamic efficiency and processing cost (PC) when the product was 95% pure propylene. However, to produce higher purity products, the membrane alone could not perform the separation, and a membrane/distillation hybrid was required. In these cases, there is an optimum amount of separation to be accomplished by the membrane (expressed as the fraction of the total availability change of the membrane/distillation hybrid that takes place in the membrane and defined as {phi}{sub m}, the thermodynamic extent of separation). Qualitative and quantitative guidelines are discussed with regard to choosing a hybrid system. 54 refs., 66 figs., 36 tabs.

  20. Spectroscopic and physicochemical measurements for on-line monitoring of used nuclear fuel separation processes

    SciTech Connect (OSTI)

    Nee, Ko; Nilsson, M. [Department of Chemical Engineering and Material Science, University of California, 916 Engineering Tower, Irvine, CA 92697-2575 (United States); Bryan, S.; Levitskaia, T. [Pacific Northwest National Laboratory, PO BOX 999, Richland, CA 99352 (United States)

    2013-07-01T23:59:59.000Z

    Separation processes for used nuclear fuel are often complicated and challenging due to the high constraints in purity of the products and safeguards of the process streams. In order to achieve a safe, secure and efficient separation process, the liquid streams in the separation process require close monitoring. Due to the high radiation environment, sampling of the materials is difficult. Availability of a detection technique that is remote, non-destructive and can avoid time-delay caused by retrieving samples would be beneficial and could minimize the exposure to personnel and provide material accountancy to avoid diversion (non-proliferation). For example, Ultra Violet (UV), Visible (Vis), Near-Infrared (NIR) and Raman spectroscopy that detect and quantify elements present in used nuclear fuel, e.g. lanthanides, actinides and molecules such as nitrate, can be used. In this work, we have carried out NIR and Raman spectroscopy to study aqueous solutions composed of different concentrations of nitric acid, sodium nitrate, and neodymium at varied temperatures. A chemometric model for online monitoring based on the PLS-Toolbox (MATLAB) software has been developed and validated to provide chemical composition of process streams based on spectroscopic data. In conclusion, both of our NIR and Raman spectra were useful for H{sup +} and NO{sub 3} prediction, and only NIR was helpful for the Nd{sup 3+} prediction.

  1. The Multi-Isotope Process Monitor Project: FY11 Progress and Accomplishments

    SciTech Connect (OSTI)

    Orton, Christopher R.; Fraga, Carlos G.; Hayes, John W.; Schwantes, Jon M.; Bender, Sarah E.; Unlu, Kenan; Dayman, Kenneth J.; Schreiber, S. S.; Landsberger, Sheldon

    2012-08-01T23:59:59.000Z

    Summary The Multi-Isotope Process (MIP) Monitor represents a potentially new and efficient approach to monitoring process conditions in reprocessing facilities with the high-level goal of aiding in the “...(minimization of) the risks of nuclear proliferation and terrorism” (Office of Technology Assessment 1995). This approach relies on multivariate analysis and gamma spectroscopy of spent fuel product and waste streams to automatically and simultaneously monitor a variety of process conditions (e.g., acid concentrations, burnup, cooling time, etc.) in near real-time (NRT). While the conceptual basis for the MIP Monitor has been shown to be effective in an aqueous reprocessing system, the fundamental approach should also be viable in a pyro-processing recycle system. The MIP Monitor may be calibrated to provide online quantitative information about process variables for process control or domestic safeguards applications; or it can simply monitor, with a built-in information barrier, for off-normal conditions in process streams, making the approach well-suited for applications were it is necessary to respect proprietary information or for international safeguards applications. Proof-of-concept simulations and experiments were performed in previous years demonstrating the validity of this tool in a laboratory setting. This report details follow-on research and development efforts sponsored by the U.S. Department of Energy Fuel Cycle Research and Development (FCR&D) related to the MIP Monitor for fiscal year 2011 (FY11).

  2. NOVEL COMPOSITE MEMBRANES FOR HYDROGEN SEPARATION IN GASIFICATION PROCESSES IN VISION 21 ENERGY PLANTS

    SciTech Connect (OSTI)

    Michael Schwartz

    2004-12-01T23:59:59.000Z

    This report describes the work performed, accomplishments and conclusion obtained from the project entitled ''Novel Composite Membranes for Hydrogen Separation in Gasification Processes in Vision 21 Energy Plants'' under the United States Department of Energy Contract DE-FC26-01NT40973. ITN Energy Systems was the prime contractor. Team members included: the Idaho National Engineering and Environmental Laboratory; Nexant Consulting; Argonne National Laboratory and Praxair. The objective of the program was to develop a novel composite membrane structure for hydrogen separation as a key technology module within the future ''Vision 21'' fossil fuel plants. The separation technology module is targeted for use within the gasification module of the ''Vision 21'' fossil fuel plant. The high performance and low-cost manufacturing of the proposed technology will benefit the deployment of ''Vision 21'' fossil fuel plant processes by improving the energy efficiency, flexibility and environmental performance of these plants. Of particular importance is that this technology will also produce a stream of pure carbon dioxide. This allows facile sequestration or other use of this greenhouse gas. These features will benefit the U.S. in allowing for the continued use of domestic fossil fuels in a more energy efficient and environmentally acceptable manner. The program developed and evaluated composite membranes and catalysts for hydrogen separation. Components of the monolithic modules were fabricated by plasma spray processing. The engineering and economic characteristics of the proposed Ion Conducting Ceramic Membrane (ICCM) approach, including system integration issues, were also assessed. This resulted in a comprehensive evaluation of the technical and economic feasibility of integration schemes of ICCM hydrogen separation technology within Vision 21 fossil fuel plants. Several results and conclusion were obtained during this program. In the area of materials synthesis, novel pyrochlore-based proton conductors were identified, synthesized and characterized. They exhibited conductivity as high as 0.03 S/cm at 900 C. Long-term stability under CO{sub 2} and H{sub 2} atmospheres was also demonstrated. In the area of membrane fabrication by plasma spray processing, the initial results showed that the pyrochlore materials could be processed in a spray torch. Although leak-tight membranes were obtained, cracking, most likely due to differences in thermal expansion, remained a problem. More modeling and experimental work can be used to solve this problem. Finally the techno-economic analyses showed that the ITN ICCM approach for separating H{sub 2} is comparable to conventional pressure swing adsorption (PSA) technology in efficiency and economics. Enhanced membrane flux and lower operating temperatures may make the ICCM approach superior to PSA.

  3. Minor actinide separation: simplification of the DIAMEX-SANEX strategy by means of novel SANEX processes

    SciTech Connect (OSTI)

    Geist, A. [Karlsruher Institut fuer Technologie - KIT, INE, P. O. Box 3640, 76021 Karlsruhe (Germany); Modolo, G.; Wilden, A.; Kaufholz, P. [Forschungszentrum Juelich GmbH, IEK-6, Juelich (Germany)

    2013-07-01T23:59:59.000Z

    The separation of An(III) from PUREX raffinate has previously been demonstrated by applying a DIAMEX process (i.e., co-extraction of An(III) and Ln(III) from HAR) followed by a SANEX process (i.e., selective extraction of An(III) from the DIAMEX product containing An(III) + Ln(III)). In line with process intensification issues, more compact processes have been developed: Recently, a 1c-SANEX process test was successfully performed, directly extracting An(III) from PUREX HAR. More recently, a new i-SANEX process was successfully tested. This process is based on the co-extraction of An(III) + Ln(III) into a TODGA solvent, followed by a selective back-extraction of An(III) by a water soluble complexing agent, in this case SO{sub 3}-Ph-BTP. In both cases, good recoveries were achieved, and very pure product solutions were obtained. However, both 1c-SANEX and i-SANEX used non-CHON chemicals. Nevertheless, these processes are a simplification to the DIAMEX + SANEX process as only one solvent is used. Finally, the new i-SANEX process is the most compact process. (authors)

  4. Measurements of Nucleon-Induced Fission Cross-Sections of Separated Tungsten Isotopes and Natural Tungsten in the 50-200 MeV Energy Region

    E-Print Network [OSTI]

    V. P. Eismont; N. P. Filatov; A. N. Smirnov; S. M. Soloviev; J. Blomgren; H. Conde; A. V. Prokofiev; S. G. Mashnik

    2005-07-07T23:59:59.000Z

    Neutron- and proton-induced fission cross-sections of separated isotopes of tungsten (182W, 183W, 184W, and 186W) and natural tungsten relative to 209Bi have been measured in the incident nucleon energy region 50-200 MeV using fission chambers based on thin-film breakdown counters (TFBC) at quasi-monoenergetic neutrons from the 7Li(p,n) reaction and at the proton beams of The Svedberg Laboratory (TSL), Uppsala University (Uppsala, Sweden). The preliminary experimental data are presented in comparison with the recent data for nuclei in the lead-bismuth region, as well as with predictions by the CEM03.01 event generator.

  5. A calcium oxide sorbent process for bulk separation of carbon dioxide

    SciTech Connect (OSTI)

    Harrison, D.P.

    1992-10-01T23:59:59.000Z

    Objective is to investigate the feasibility of a high-temperature, high-pressure process for bulk separation of CO[sub 2] from coal- derived gas. An electrobalance reactor was used in Phase I; in Phase II, the switch was made to a fixed-bed reactor with capability for feed and product gas analysis. A gas chromatograph was delivered, installed, and operator training carried out. The sampling valve sequence is discussed.

  6. A calcium oxide sorbent process for bulk separation of carbon dioxide

    SciTech Connect (OSTI)

    Harrison, D.P.

    1992-04-01T23:59:59.000Z

    This research project is investigating the technical feasibility of a high-temperature, high-pressure process for the bulk separation of CO[sub 2] from coal-derived gas. Phase I consisted of 6 tasks. Phase II added a seventh task to the project. This report is limited to a description of the final experimental results obtained in Phase I, Task 5 (multicycle tests), and a brief overview of justification and plans for Phase II, Task 7.

  7. Isotope Tracer Studies of Diffusion in Sillicates and of Geological Transport Processes Using Actinide Elements

    SciTech Connect (OSTI)

    Wasserburg, Gerald J

    2008-07-31T23:59:59.000Z

    The objectives were directed toward understanding the transport of chemical species in nature, with particular emphasis on aqueous transport in solution, in colloids, and on particles. Major improvements in measuring ultra-low concentrations of rare elements were achieved. We focused on two areas of studies: (1) Field, laboratory, and theoretical studies of the transport and deposition of U, Th isotopes and their daughter products in natural systems; and (2) Study of calcium isotope fractionation effects in marine carbonates and in carbonates precipitated in the laboratory, under controlled temperature, pH, and rates of precipitation. A major study of isotopic fractionation of Ca during calcite growth from solution has been completed and published. It was found that the isotopic shifts widely reported in the literature and attributed to biological processes are in fact due to a small equilibrium fractionation factor that is suppressed by supersaturation of the solution. These effects were demonstrated in the laboratory and with consideration of the solution conditions in natural systems, where [Ca{sup 2+}] >> [CO{sub 3}{sup 2-}] + [HCO{sub 3}{sup -}]. The controlling rate is not the diffusion of Ca, as was earlier proposed, but rather the rate of supply of [CO{sub 3}{sup 2-}] ions to the interface. This now opens the issues of isotopic fractionation of many elements to a more physical-chemical approach. The isotopic composition of Ca {Delta}({sup 44}Ca/{sup 40}Ca) in calcite crystals has been determined relative to that in the parent solutions by TIMS using a double spike. Solutions were exposed to an atmosphere of NH{sub 3} and CO{sub 2}, provided by the decomposition of (NH4)2CO3. Alkalinity, pH, and concentrations of CO{sub 3}{sup 2-}, HCO{sub 3}{sup -}, and CO{sub 2} in solution were determined. The procedures permitted us to determine {Delta}({sup 44}Ca/{sup 40}Ca) over a range of pH conditions, with the associated ranges of alkalinity. Two solutions with greatly different Ca concentrations were used, but, in all cases, the condition [Ca] >> [CO{sub 3}{sup 2-}] was met. A wide range in {Delta}({sup 44}Ca/{sup 40}Ca) was found for the calcite crystals, extending from 0.04 {+-} 0.13 to -1.34 {+-} 0.15 {per_thousand}, generally anticorrelating with the amount of Ca removed from the solution. The results show that {Delta}({sup 44}Ca/{sup 40}Ca) is a linear function of the saturation state of the solution with respect to calcite ({Omega}). The two parameters are very well correlated over a wide range in {Omega} for each solution with a given [Ca]. Solutions, which were vigorously stirred, showed a much smaller range in {Delta}({sup 44}Ca/{sup 40}Ca) and gave values of -0.42 {+-} 0.14 {per_thousand}, with the largest effect at low {Omega}. It is concluded that the diffusive flow of CO{sub 3}{sup 2-} into the immediate neighborhood of the crystal-solution interface is the rate-controlling mechanism and that diffusive transport of Ca{sup 2+} is not a significant factor. The data are simply explained by the assumptions that: (a) the immediate interface of the crystal and the solution is at equilibrium with {Delta}({sup 44}Ca/{sup 40}Ca) {approx} -1.5 {+-} 0.25 {per_thousand}, and (b) diffusive inflow of CO{sub 3}{sup 2-} causes supersaturation, thus precipitating Ca from the regions, exterior to the narrow zone of equilibrium. We consider this model to be a plausible explanation of the available data reported in the literature. The well-resolved but small and regular isotope fractionation shifts in Ca are thus not related to the diffusion of very large hydrated Ca complexes, but rather due to the ready availability of Ca in the general neighborhood of the crystal solution interface. The largest isotopic shift which occurs is a small equilibrium effect which is then subdued by supersaturation precipitation for solutions where [Ca{sup 2+}] >> [CO{sub 3}{sup 2-}] + [HCO{sub 3}{sup -}]. It is shown that there is a clear temperature dependence of the net isotopic shifts, which is simply due to changes in {Omega}

  8. Process and apparatus for separation of components of a gas stream

    SciTech Connect (OSTI)

    Bryan, Charles R.; Torczynski, John R.; Brady, Patrick V.; Gallis, Michail; Brooks, Carlton F.

    2014-06-17T23:59:59.000Z

    A process and apparatus for separating a gas mixture comprising providing a slot in a gas separation channel (conceptualized as a laterally elongated Clusius-Dickel column), having a length through which a net cross-flow of the gas mixture may be established; applying a higher temperature to one side of the channel and a lower temperature on an opposite side of the channel thereby causing thermal-diffusion and buoyant-convection flow to occur in the slot; and establishing a net cross-flow of a gas mixture comprising at least one higher density gas component and at least one lower density gas component along the length of the slot, wherein the cross-flow causes, in combination with the convection flow, a spiraling flow in the slot; and wherein the spiral flow causes an increasing amount of separation of the higher density gas from the lower density gas along the length of the channel. The process may use one or more slots and/or channels.

  9. Process and apparatus for separation of components of a gas stream

    SciTech Connect (OSTI)

    Bryan, Charles R; Torczynski, John R; Brady, Patrick V; Gallis, Michail; Brooks, Carlton F

    2013-11-19T23:59:59.000Z

    A process and apparatus for separating a gas mixture comprising providing a slot in a gas separation channel (conceptualized as a laterally elongated Clusius-Dickel column), having a length through which a net cross-flow of the gas mixture may be established; applying a higher temperature to one side of the channel and a lower temperature on an opposite side of the channel thereby causing thermal-diffusion and buoyant-convection flow to occur in the slot; and establishing a net cross-flow of a gas mixture comprising at least one higher density gas component and at least one lower density gas component along the length of the slot, wherein the cross-flow causes, in combination with the convection flow, a spiraling flow in the slot; and wherein the spiral flow causes an increasing amount of separation of the higher density gas from the lower density gas along the length of the channel. The process may use one or more slots and/or channels.

  10. Process and apparatus for separation of components of a gas stream

    SciTech Connect (OSTI)

    Bryan, Charles R; Torczynski, John R; Brady, Patrick V; Gallis, Michail; Brooks, Carlton F

    2013-09-17T23:59:59.000Z

    A process and apparatus for separating a gas mixture comprising providing a slot in a gas separation channel (conceptualized as a laterally elongated Clusius-Dickel column), having a length through which a net cross-flow of the gas mixture may be established; applying a higher temperature to one side of the channel and a lower temperature on an opposite side of the channel thereby causing thermal-diffusion and buoyant-convection flow to occur in the slot; and establishing a net cross-flow of a gas mixture comprising at least one higher density gas component and at least one lower density gas component along the length of the slot, wherein the cross-flow causes, in combination with the convection flow, a spiraling flow in the slot; and wherein the spiral flow causes an increasing amount of separation of the higher density gas from the lower density gas along the length of the channel. The process may use one or more slots and/or channels.

  11. Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Paducah Gaseous Diffusion Plant site

    SciTech Connect (OSTI)

    Marmer, G.J.; Dunn, C.P.; Moeller, K.L.; Pfingston, J.M.; Policastro, A.J.; Yuen, C.R.; Cleland, J.H. (ed.)

    1991-09-01T23:59:59.000Z

    Uranium enrichment in the United States has utilized a diffusion process to preferentially enrich the U-235 isotope in the uranium product. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. The U-235 atoms are ionized when precisely tuned laser light -- of appropriate power, spectral, and temporal characteristics -- illuminates the uranium vapor and selectively photoionizes the U-235 isotope. A programmatic document for use in screening DOE site to locate a U-AVLIS production plant was developed and implemented in two parts. The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the PGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. 65 refs., 15 tabs.

  12. NOVEL COMPOSITE MEMBRANES FOR HYDROGEN SEPARATION IN GASIFICATION PROCESSES IN VISION 21 ENERGY PLANTS

    SciTech Connect (OSTI)

    Michael Schwartz

    2004-01-01T23:59:59.000Z

    ITN Energy Systems, along with its team members, the Idaho National Engineering and Environmental Laboratory, Nexant Consulting, Argonne National Laboratory and Praxair, propose to develop a novel composite membrane structure for hydrogen separation as a key technology module within the future ''Vision 21'' fossil fuel plants. The ITN team is taking a novel approach to hydrogen separation membrane technology where fundamental engineering material development is fully integrated into fabrication designs; combining functionally graded materials, monolithic module concept and plasma spray manufacturing techniques. The technology is based on the use of Ion Conducting Ceramic Membranes (ICCM) for the selective transport of hydrogen. The membranes are comprised of composites consisting of a proton conducting ceramic and a second metallic phase to promote electrical conductivity. Functional grading of the membrane components allows the fabrication of individual membrane layers of different materials, microstructures and functions directly into a monolithic module. Plasma spray techniques, common in industrial manufacturing, are well suited for fabricating ICCM hydrogen separation modules inexpensively, yielding compact membrane modules that are amenable to large scale, continuous manufacturing with low costs. This program will develop and evaluate composite membranes and catalysts for hydrogen separation. Components of the monolithic modules will be fabricated by plasma spray processing. The engineering and economic characteristics of the proposed ICCM approach, including system integration issues, will also be assessed. This will result in a complete evaluation of the technical and economic feasibility of ICCM hydrogen separation for implementation within the ''Vision 21'' fossil fuel plant. The ICCM hydrogen separation technology is targeted for use within the gasification module of the ''Vision 21'' fossil fuel plant. The high performance and low-cost manufacturing of the proposed technology will benefit the deployment of ''Vision 21'' fossil fuel plant processes by improving the energy efficiency, flexibility and environmental performance of these plants. Of particular importance is that this technology will also produce a stream of pure carbon dioxide. This allows facile sequestration or other use of this greenhouse gas. These features will benefit the U.S. in allowing for the continued use of domestic fossil fuels in a more energy efficient and environmentally acceptable manner.

  13. NOVEL COMPOSITE MEMBRANES FOR HYDROGEN SEPARATION IN GASIFICATION PROCESSES IN VISION 21 ENERGY PLANTS

    SciTech Connect (OSTI)

    Michael Schwartz

    2003-07-01T23:59:59.000Z

    ITN Energy Systems, along with its team members, the Idaho National Engineering and Environmental Laboratory, Nexant Consulting, Argonne National Laboratory and Praxair, propose to develop a novel composite membrane structure for hydrogen separation as a key technology module within the future ''Vision 21'' fossil fuel plants. The ITN team is taking a novel approach to hydrogen separation membrane technology where fundamental engineering material development is fully integrated into fabrication designs; combining functionally graded materials, monolithic module concept and plasma spray manufacturing techniques. The technology is based on the use of Ion Conducting Ceramic Membranes (ICCM) for the selective transport of hydrogen. The membranes are comprised of composites consisting of a proton conducting ceramic and a second metallic phase to promote electrical conductivity. Functional grading of the membrane components allows the fabrication of individual membrane layers of different materials, microstructures and functions directly into a monolithic module. Plasma spray techniques, common in industrial manufacturing, are well suited for fabricating ICCM hydrogen separation modules inexpensively, yielding compact membrane modules that are amenable to large scale, continuous manufacturing with low costs. This program will develop and evaluate composite membranes and catalysts for hydrogen separation. Components of the monolithic modules will be fabricated by plasma spray processing. The engineering and economic characteristics of the proposed ICCM approach, including system integration issues, will also be assessed. This will result in a complete evaluation of the technical and economic feasibility of ICCM hydrogen separation for implementation within the ''Vision 21'' fossil fuel plant. The ICCM hydrogen separation technology is targeted for use within the gasification module of the ''Vision 21'' fossil fuel plant. The high performance and low-cost manufacturing of the proposed technology will benefit the deployment of ''Vision 21'' fossil fuel plant processes by improving the energy efficiency, flexibility and environmental performance of these plants. Of particular importance is that this technology will also produce a stream of pure carbon dioxide. This allows facile sequestration or other use of this greenhouse gas. These features will benefit the U.S. in allowing for the continued use of domestic fossil fuels in a more energy efficient and environmentally acceptable manner.

  14. NOVEL COMPOSITE MEMBRANES FOR HYDROGEN SEPARATION IN GASIFICATION PROCESSES IN VISION 21 ENERGY PLANTS

    SciTech Connect (OSTI)

    Michael Schwartz

    2003-10-01T23:59:59.000Z

    ITN Energy Systems, along with its team members, the Idaho National Engineering and Environmental Laboratory, Nexant Consulting, Argonne National Laboratory and Praxair, propose to develop a novel composite membrane structure for hydrogen separation as a key technology module within the future ''Vision 21'' fossil fuel plants. The ITN team is taking a novel approach to hydrogen separation membrane technology where fundamental engineering material development is fully integrated into fabrication designs; combining functionally graded materials, monolithic module concept and plasma spray manufacturing techniques. The technology is based on the use of Ion Conducting Ceramic Membranes (ICCM) for the selective transport of hydrogen. The membranes are comprised of composites consisting of a proton conducting ceramic and a second metallic phase to promote electrical conductivity. Functional grading of the membrane components allows the fabrication of individual membrane layers of different materials, microstructures and functions directly into a monolithic module. Plasma spray techniques, common in industrial manufacturing, are well suited for fabricating ICCM hydrogen separation modules inexpensively, yielding compact membrane modules that are amenable to large scale, continuous manufacturing with low costs. This program will develop and evaluate composite membranes and catalysts for hydrogen separation. Components of the monolithic modules will be fabricated by plasma spray processing. The engineering and economic characteristics of the proposed ICCM approach, including system integration issues, will also be assessed. This will result in a complete evaluation of the technical and economic feasibility of ICCM hydrogen separation for implementation within the ''Vision 21'' fossil fuel plant. The ICCM hydrogen separation technology is targeted for use within the gasification module of the ''Vision 21'' fossil fuel plant. The high performance and low-cost manufacturing of the proposed technology will benefit the deployment of ''Vision 21'' fossil fuel plant processes by improving the energy efficiency, flexibility and environmental performance of these plants. Of particular importance is that this technology will also produce a stream of pure carbon dioxide. This allows facile sequestration or other use of this greenhouse gas. These features will benefit the U.S. in allowing for the continued use of domestic fossil fuels in a more energy efficient and environmentally acceptable manner.

  15. Process and apparatus for separating fine particles by microbubble flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, Roe-Hoan (Blacksburg, VA); Adel, Gregory T. (Blacksburg, VA); Luttrell, Gerald H. (Blacksburg, VA)

    1991-01-01T23:59:59.000Z

    A method and apparatus are disclosed for the microbubble flotation separation of very fine particles, especially coal, so as to produce a high purity and large recovery efficiently. This is accomplished through the use of a high aspect ratio flotation column, microbubbles, and a countercurrent use of wash water to gently wash the froth. Also, disclosed are unique processes and apparatus for generating microbubbles for flotation in a high efficient and inexpensive manner using either a porous tube or an in-line static generator.

  16. Process and apparatus for separating fine particles by microbubble flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, R.H.; Adel, G.T.; Luttrell, G.H.

    1991-01-01T23:59:59.000Z

    A method and apparatus are disclosed for the microbubble flotation separation of very fine particles, especially coal, so as to produce a high purity and large recovery efficiently. This is accomplished through the use of a high aspect ratio flotation column, microbubbles, and a countercurrent use of wash water to gently wash the froth. Also, disclosed are unique processes and apparatus for generating microbubbles for flotation in a high efficient and inexpensive manner using either a porous tube or an in-line static generator. 23 figures.

  17. Isotope Science and Production

    E-Print Network [OSTI]

    Isotope Science and Production 35 years of experience in isotope production, processing, and applications. Llllll Committed to the safe and reliable production of radioisotopes, products, and services nuclear materials in trucks and cargo containers. Isotopes for Threat Reduction Isotope production at Los

  18. An Ionic Liquid Reaction and Separation Process for Production of Hydroxymethylfurfural from Sugars

    SciTech Connect (OSTI)

    Liu, Wei; Zheng, Feng; Li, Joanne; Cooper, Alan R.

    2014-01-01T23:59:59.000Z

    There has been world-wide interest to making plastics out of renewable biomass feedstock for recent years. Hydroxymethylfurfural (HMF) is viewed as an attractive alternate to terephthalic acid (TPA) for production of polyesters (PET) and polyamides. Conversion of sugars into HMF has been studied in numerous publications. In this work, a complete ionic liquid reaction and separation process is presented for nearly stoichiometric conversion of fructose into HMF. Different adsorbent materials are evaluated and silicalite material is demonstrated effective for isolation of 99% pure HMF from actual ionic liquid reaction mixtures and for recovery of the un-converted sugars and reaction intermediate along with the ionic liquid. Membrane-coated silicalite particles are prepared and studied for a practical adsorption process operated at low pressure drops but with separation performances comparable or better than the powder material. Complete conversion of fresh fructose feed into HMF in the recycled ionic liquid is shown under suitable reaction conditions. Stability of HMF product is characterized. A simplified process flow diagram is proposed based on these research results, and the key equipment such as reactor and adsorbent bed is sized for a plant of 200,000 ton/year of fructose processing capacity. The proposed HMF production process is much simpler than the current paraxylene (PX) manufacturing process from petroleum oil, which suggests substantial reduction to the capital cost and energy consumption be possible. At the equivalent value to PX on the molar basis, there can be a large gross margin for HMF production from fructose and/or sugars.

  19. The Multi-Isotope Process (MIP) Monitor Project: FY13 Final Report...

    Office of Scientific and Technical Information (OSTI)

    streams of a nuclear reprocessing facility. These isotopes are monitored online by gamma spectrometry and compared, in near-real-time, to spectral patterns representing "normal"...

  20. Efficient gas-separation process to upgrade dilute methane stream for use as fuel

    DOE Patents [OSTI]

    Wijmans, Johannes G. (Menlo Park, CA); Merkel, Timothy C. (Menlo Park, CA); Lin, Haiqing (Mountain View, CA); Thompson, Scott (Brecksville, OH); Daniels, Ramin (San Jose, CA)

    2012-03-06T23:59:59.000Z

    A membrane-based gas separation process for treating gas streams that contain methane in low concentrations. The invention involves flowing the stream to be treated across the feed side of a membrane and flowing a sweep gas stream, usually air, across the permeate side. Carbon dioxide permeates the membrane preferentially and is picked up in the sweep air stream on the permeate side; oxygen permeates in the other direction and is picked up in the methane-containing stream. The resulting residue stream is enriched in methane as well as oxygen and has an EMC value enabling it to be either flared or combusted by mixing with ordinary air.

  1. Multi-gravity separator: an alternate gravity concentrator to process coal fines

    SciTech Connect (OSTI)

    Majumder, A.K.; Bhoi, K.S.; Barnwal, J.P. [Regional Research Laboratories, Bhopal (India)

    2007-08-15T23:59:59.000Z

    The multi-gravity separator (MGS) is a novel piece of equipment for the separation of fine and ultra-fine minerals. However, the published literature does not demonstrate its use in the separation of coal fines. Therefore, an attempt was made to study the effects of different process variables on the performance of an MGS for the beneficiation of coal fines. The results obtained from this study revealed that among the parameters studied, drum rotation and feed solids concentration play dominating roles in controlling the yield and ash content of the clean coal. Mathematical modeling equations that correlate the variables studied and the yield and ash contents of the clean coal were developed to predict the performance of an MGS under different operating and design conditions. The entire exercise revealed that the MGS could produce a clean coal with an ash content of 14.67% and a yield of 71.23% from a feed coal having an ash content of 24.61 %.

  2. VERIFICATION SURVEY ACTIVITIES IN FS SURVEY UNITS 7, 8, 9, 10, 11, 13 & 14 AT THE SEPARATIONS PROCESS RESEARCH UNIT

    SciTech Connect (OSTI)

    M.G. JADICK

    2010-05-26T23:59:59.000Z

    FINAL INTERIM REPORT VERIFICATION SURVEY ACTIVITIES IN FINAL STATUS SURVEY UNITS 7, 8, 9, 10, 11, 13 AND 14 AT THE SEPARATIONS PROCESS RESEARCH UNIT, Niskayuna, New York 0496-SR-03-0. The Separations Process Research Unit (SPRU) facilities were constructed in the late 1940s to research the chemical separation of plutonium and uranium. SPRU operated between February 1950 and October 1953. The research activities ceased following the successful development of the reduction/oxidation and plutonium/uranium extraction processes that were subsequently used by the Hanford and the Savannah River sites.

  3. Rolling Process Modeling Report: Finite-Element Prediction of Roll Separating Force and Rolling Defects

    SciTech Connect (OSTI)

    Soulami, Ayoub; Lavender, Curt A.; Paxton, Dean M.; Burkes, Douglas

    2014-04-23T23:59:59.000Z

    Pacific Northwest National Laboratory (PNNL) has been investigating manufacturing processes for the uranium-10% molybdenum (U-10Mo) alloy plate-type fuel for the U.S. high-performance research reactors. This work supports the Convert Program of the U.S. Department of Energy’s National Nuclear Security Administration (DOE/NNSA) Global Threat Reduction Initiative. This report documents modeling results of PNNL’s efforts to perform finite-element simulations to predict roll separating forces and rolling defects. Simulations were performed using a finite-element model developed using the commercial code LS-Dyna. Simulations of the hot rolling of U-10Mo coupons encapsulated in low-carbon steel have been conducted following two different schedules. Model predictions of the roll-separation force and roll-pack thicknesses at different stages of the rolling process were compared with experimental measurements. This report discusses various attributes of the rolled coupons revealed by the model (e.g., dog-boning and thickness non-uniformity).

  4. Novel Composite Membranes for Hydrogen Separation in Gasification Processes in Vision 21 Energy Plants

    SciTech Connect (OSTI)

    Schwartz, Michael

    2001-11-06T23:59:59.000Z

    ITN Energy Systems, Inc. (ITN) and its partners, the Idaho National Engineering and Environmental Laboratory, Argonne National Laboratory, Nexant Consulting, LLC and Praxair, Inc. are developing composite membranes for hydrogen separation as a key technology module within the future ''Vision 21'' fossil fuel plants. The ITN team is pursuing a novel approach to hydrogen separation membrane technology where fundamental engineering material development is fully integrated into module fabrication designs; combining functionally-graded materials, monolithic module concept and thermal spray manufacturing techniques. The technology is based on the use of Ion Conducting Ceramic Membranes (ICCM) for the selective transport of hydrogen. The membranes are comprised of composites consisting of a proton conducting ceramic and a second metallic phase to promote electrical conductivity. Functional grading of the membrane components allows for the fabrication of individual membrane layers of different materials, microstructures and functions directly into a monolithic module. Plasma spray techniques, common in industrial manufacturing, are well suited for fabricating ICCM hydrogen separation modules inexpensively, yielding compact membrane modules that are amenable to large scale, continuous manufacturing techniques with low costs. The engineering and economic characteristics of the proposed ICCM approach, including system integration issues, are being assessed. This will result in an evaluation of the technical and economic feasibility of the proposed ICCM hydrogen separation approach for implementation within the ''Vision 21'' fossil fuel plant. The ICCM hydrogen separation technology is targeted for use within the gasification module of the ''Vision 21'' fossil fuel plant. The high performance and low-cost manufacturing of the proposed technology will benefit the deployment of ''Vision 21'' fossil fuel plant processes by improving the energy efficiency, flexibility and environmental performance of such plants. Of particular importance is that the proposed technology also results in a stream of pure carbon dioxide. This allows for the facile sequestration or other use of this greenhouse gas. These features will benefit the U.S. in allowing for the continued use of domestic fossil fuels in a more energy efficient and environmentally acceptable manner.

  5. Evaluation, engineering and development of advanced cyclone processes. Final separating media evaluation and test report (FSMER). Appendices

    SciTech Connect (OSTI)

    NONE

    1996-05-01T23:59:59.000Z

    This report consists of appendices pertaining to the separating media evaluation (calcium nitrate solution) and testing for an advanced cyclone process. Appendices include: materials safety data, aqueous medium regeneration, pH control strategy, and other notes and data.

  6. Gas separation process using membranes with permeate sweep to remove CO.sub.2 from gaseous fuel combustion exhaust

    DOE Patents [OSTI]

    Wijmans Johannes G. (Menlo Park, CA); Merkel, Timothy C. (Menlo Park, CA); Baker, Richard W. (Palo Alto, CA)

    2012-05-15T23:59:59.000Z

    A gas separation process for treating exhaust gases from the combustion of gaseous fuels, and gaseous fuel combustion processes including such gas separation. The invention involves routing a first portion of the exhaust stream to a carbon dioxide capture step, while simultaneously flowing a second portion of the exhaust gas stream across the feed side of a membrane, flowing a sweep gas stream, usually air, across the permeate side, then passing the permeate/sweep gas back to the combustor.

  7. Plasma Separation Process: Betacell (BCELL) code: User's manual. [Bipolar barrier junction

    SciTech Connect (OSTI)

    Taherzadeh, M.

    1987-11-13T23:59:59.000Z

    The emergence of clearly defined applications for (small or large) amounts of long-life and reliable power sources has given the design and production of betavoltaic systems a new life. Moreover, because of the availability of the plasma separation program, (PSP) at TRW, it is now possible to separate the most desirable radioisotopes for betacell power generating devices. A computer code, named BCELL, has been developed to model the betavoltaic concept by utilizing the available up-to-date source/cell parameters. In this program, attempts have been made to determine the betacell energy device maximum efficiency, degradation due to the emitting source radiation and source/cell lifetime power reduction processes. Additionally, comparison is made between the Schottky and PN junction devices for betacell battery design purposes. Certain computer code runs have been made to determine the JV distribution function and the upper limit of the betacell generated power for specified energy sources. A Ni beta emitting radioisotope was used for the energy source and certain semiconductors were used for the converter subsystem of the betacell system. Some results for a Promethium source are also given here for comparison. 16 refs.

  8. Modeling atmospheric stable water isotopes and the potential for constraining cloud processes and

    E-Print Network [OSTI]

    a significant part of the observed offset from pure Rayleigh distillation. Isotope fields are shown cycle. These ratios are primarily affected by the fractionation occurring at changes of phase

  9. A NEW PROCESS DEVELOPED FOR SEPARATION OF LIGNIN FROM AMMONIUM HYDROXIDE PRETREATMENT SOLUTIONS

    SciTech Connect (OSTI)

    Sherman, S.; Gorensek, M.; Milliken, C.

    2010-12-14T23:59:59.000Z

    A method is described for separating lignin from liquid solutions resulting from the pretreatment of lignocellulosic materials such as switchgrass with ammonium hydroxide. The method involves a sequence of steps including acidification, evaporation, and precipitation or centrifugation that are performed under defined conditions, and results in a relatively pure, solid lignin product. The method is tested on ammonium hydroxide solutions containing lignin extracted from switchgrass. Experimental results show that the method is capable of recovering between 66-95% of dissolved lignin as a precipitated solid. Cost estimates of pilot-scale and industrial-scale expressions of the process indicate that breakeven lignin prices of $2.36/kg and $0.78/kg, respectively, may be obtainable with this recovery method.

  10. Inferences from the vertical distribution of Fe isotopic compositions1 on pedogenetic processes in soils2

    E-Print Network [OSTI]

    Boyer, Edmond

    studied using Fe isotopes and classical soil parameters.4 In the Cambisol, Fe transfer is limited; in-situ in soils2 Z. Fekiacova1 , S. Pichat2 , S. Cornu1 and J. Balesdent1 3 4 5 1 INRA - UR1119 Géochimie des sols.geoderma.2013.06.007 #12;2 ABSTRACT1 The isotopic compositions of major elements in soils can help understand

  11. Method for sequential injection of liquid samples for radioisotope separations

    DOE Patents [OSTI]

    Egorov, Oleg B. (Richland, WA); Grate, Jay W. (West Richland, WA); Bray, Lane A. (Richland, WA)

    2000-01-01T23:59:59.000Z

    The present invention is a method of separating a short-lived daughter isotope from a longer lived parent isotope, with recovery of the parent isotope for further use. Using a system with a bi-directional pump and one or more valves, a solution of the parent isotope is processed to generate two separate solutions, one of which contains the daughter isotope, from which the parent has been removed with a high decontamination factor, and the other solution contains the recovered parent isotope. The process can be repeated on this solution of the parent isotope. The system with the fluid drive and one or more valves is controlled by a program on a microprocessor executing a series of steps to accomplish the operation. In one approach, the cow solution is passed through a separation medium that selectively retains the desired daughter isotope, while the parent isotope and the matrix pass through the medium. After washing this medium, the daughter is released from the separation medium using another solution. With the automated generator of the present invention, all solution handling steps necessary to perform a daughter/parent radionuclide separation, e.g. Bi-213 from Ac-225 "cow" solution, are performed in a consistent, enclosed, and remotely operated format. Operator exposure and spread of contamination are greatly minimized compared to the manual generator procedure described in U.S. patent application Ser. No. 08/789,973, now U.S. Pat. No. 5,749,042, herein incorporated by reference. Using 16 mCi of Ac-225 there was no detectable external contamination of the instrument components.

  12. Isotope production and distribution Programs Fiscal Year (FY) 1995 Financial Statement Audit (ER-FC-96-01)

    SciTech Connect (OSTI)

    NONE

    1996-02-12T23:59:59.000Z

    The charter of the Department of Energy (DOE) Isotope Production and Distribution Program (Isotope Program) covers the production and sale of radioactive and stable isotopes, associated byproducts, surplus materials such as lithium and deuterium, and related isotope services. Services provided include, but are not limited to, irradiation services, target preparation and processing, source encapsulation and other special preparations, analyses, chemical separations, and leasing of stable isotopes for research purposes. Isotope Program products and services are sold worldwide for use in a wide variety of research, development, biomedical, and industrial applications. The Isotope Program reports to the Director of the Office of Nuclear Energy, Science and Technology. The Isotope Program operates under a revolving fund, as established by the Fiscal Year 1990 Energy and Water Appropriations Act (Public Law 101-101). The Fiscal Year 1995 Appropriations Act (Public Law 103-316) modified predecessor acts to allow prices charged for Isotope Program products and services to be based on production costs, market value, the needs of the research community, and other factors. Prices set for small-volume, high-cost isotopes that are needed for research may not achieve full-cost recovery. Isotope Program costs are financed by revenues from the sale of isotopes and associated services and through payments from the isotope support decision unit, which was established in the DOE fiscal year 1995 Energy, Supply, Research, and Development appropriation. The isotope decision unit finances the production and processing of unprofitable isotopes that are vital to the national interest.

  13. Experimental studies of the transfer phenomena of tritium in an isotope exchange column for recovery tritium

    E-Print Network [OSTI]

    Experimental studies of the transfer phenomena of tritium in an isotope exchange column for recovery tritium Anisia Bornea, Ion Cristescu, Marius Zamfirache, Carmen Varlam National Institute of R processes for tritium separation, is the catalyst isotope exchange water-hydrogen. The main problem

  14. Selective Separation of Trivalent Actinides from Lanthanides by Aqueous Processing with Introduction of Soft Donor Atoms

    SciTech Connect (OSTI)

    Kenneth L. Nash; Sue B. Clark; Gregg Lumetta

    2009-09-23T23:59:59.000Z

    With increased application of MOX fuels and longer burnup times for conventional fuels, higher concentrations of the transplutonium actinides Am and Cm (and even heavier species like Bk and Cf) will be produced. The half-lives of the Am isotopes are significantly longer than those of the most important long-lived, high specific activity lanthanides or the most common Cm, Bk and Cf isotopes, thus the greatest concern as regards long-term radiotoxicity. With the removal and transmutation of Am isotopes, radiation levels of high level wastes are reduced to near uranium mineral levels within less than 1000 years as opposed to the time-fram if they remain in the wastes.

  15. Approved Module Information for CE2103, 2014/5 Module Title/Name: Separation Processes Module Code: CE2103

    E-Print Network [OSTI]

    Neirotti, Juan Pablo

    processes involving unit operations * Design and sizing of a binary mixture distillation column Indicative of fundamental separation processes * an introduction to the techniques used for the preliminary design of distillation, gas absorption and cooling tower. * Knowledge of the fundamentals and practical applications

  16. The production of fuels and chemicals from food processing wastes using a novel fermenter separator

    SciTech Connect (OSTI)

    Dale, M.C.; Venkatesh, K.V.; Choi, Hojoon; Moelhman, M.; Saliceti, L.; Okos, M.R.; Wankat, P.C.

    1991-12-01T23:59:59.000Z

    During 1991, considerable progress was made on the waste utilization project. Two small Wisconsin companies have expressed an interest in promoting and developing the ICRS technology. Pilot plant sites at (1) Hopkinton, IA, for a sweet whey plant, and Beaver Dam WI, for an acid whey site have been under development siting ICRS operations. The Hopkinton, IA site is owned and operated by Permeate Refining Inc., who have built a batch ethanol plant across the street from Swiss Valley Farms cheddar cheese operations. Permeate from Swiss Valley is piped across to PRI. PRI has signed a contract to site a 300--500,000 gallon/yr to ICRS pilot plant. They feel that the lower labor, lower energy, continuous process offered by the ICRS will substantially improve their profitability. Catalytics, Inc, is involved with converting whey from a Kraft cream cheese operation to ethanol and yeast. A complete project including whey concentration, sterilization, and yeast growth has been designed for this site. Process design improvements with the ICRS focussed on ethanol recovery techniques during this year's project. A solvent absorption/extractive distillation (SAED) process has been developed which offers the capability of obtaining an anhydrous ethanol product from vapors off 3 to 9% ethanol solutions using very little energy for distillation. Work on products from waste streams was also performed. a. Diacetyl as a high value flavor compound was very successfully produced in a Stirred Tank Reactor w/Separation. b. Yeast production from secondary carbohydrates in the whey, lactic acid, and glycerol was studied. c. Lactic acid production from cellulose and lactose studies continued. d. Production of anti-fungal reagents by immobilized plant cells; Gossypol has antifungal properties and is produced by G. arboretum.

  17. Proceedings of the Efficient Separations and Processing Cross-Cutting Program Annual Technical Exchange Meeting

    SciTech Connect (OSTI)

    NONE

    1995-02-01T23:59:59.000Z

    This document contains summaries of technology development presented at the 1995 Efficient Separations and Processing Cross-Cutting Program (ESP) Annual Technical Exchange Meeting. The ESP is sponsored by the US Department of Energy`s Office of Environmental Management (EM), Office of Technology Development. The meeting is held annually to promote a free exchange of ideas among technology developers, potential users (for example, EM focus areas), and other interested parties within EM. During this meeting, developers of ESP-funded technologies describe the problems and needs addressed by their technologies; the technical approach, accomplishments, and resolution of issues; the strategy and schedule for commercialization; and evolving potential applications. Presenters are asked to address the following areas: Target waste management problem, waste stream, or data need; scientific background and technical approach; technical accomplishments and resolution of technical issues; schedule and strategy for commercializing and implementing the technology or acquiring needed data; potential alternate applications of the technology or data, including outside of DOE/EM. The meeting is not a program review of the individual tasks or subtasks; but instead focuses on the technical aspects and implementation of ESP-sponsored technology or data. The meeting is also attended by members of the ESP Technical Review Team, who have the opportunity at that time to review the ESP as a whole.

  18. Waste Heat Recovery and Recycling in Thermal Separation Processes: Distillation, Multi-Effect Evaporation (MEE) and Crystallization Processes

    SciTech Connect (OSTI)

    Emmanuel A. Dada; Chandrakant B. Panchal; Luke K. Achenie; Aaron Reichl; Chris C. Thomas

    2012-12-03T23:59:59.000Z

    Evaporation and crystallization are key thermal separation processes for concentrating and purifying inorganic and organic products with energy consumption over 1,000 trillion Btu/yr. This project focused on a challenging task of recovering low-temperature latent heat that can have a paradigm shift in the way thermal process units will be designed and operated to achieve high-energy efficiency and significantly reduce the carbon footprint as well as water footprint. Moreover, this project has evaluated the technical merits of waste-heat powered thermal heat pumps for recovery of latent heat from distillation, multi-effect evaporation (MEE), and crystallization processes and recycling into the process. The Project Team has estimated the potential energy, economics and environmental benefits with the focus on reduction in CO2 emissions that can be realized by 2020, assuming successful development and commercialization of the technology being developed. Specifically, with aggressive industry-wide applications of heat recovery and recycling with absorption heat pumps, energy savings of about 26.7 trillion Btu/yr have been estimated for distillation process. The direct environmental benefits of this project are the reduced emissions of combustible products. The estimated major reduction in environmental pollutants in the distillation processes is in CO2 emission equivalent to 3.5 billion lbs/year. Energy consumption associated with water supply and treatments can vary between 1,900 kWh and 23,700 kWh per million-gallon water depending on sources of natural waters [US DOE, 2006]. Successful implementation of this technology would significantly reduce the demand for cooling-tower waters, and thereby the use and discharge of water treatment chemicals. The Project Team has also identified and characterized working fluid pairs for the moderate-temperature heat pump. For an MEE process, the two promising fluids are LiNO3+KNO3+NANO3 (53:28:19 ) and LiNO3+KNO3+NANO2(53:35:12). And for an H2O2 distillation process, the two promising fluids are Trifluoroethanol (TFE) + Triethylene Glycol Dimethyl ether (DMETEG) and Ammonia+ Water. Thermo-physical properties calculated by Aspen+ are reasonably accurate. Documentation of the installation of pilot-plants or full commercial units were not found in the literature for validating thermo-physical properties in an operating unit. Therefore, it is essential to install a pilot-scale unit to verify thermo-physical properties of working fluid pairs and validate the overall efficiency of the thermal heat pump at temperatures typical of distillation processes. For an HO2 process, the ammonia-water heat pump system is more compact and preferable than the TFE-DMETEG heat pump. The ammonia-water heat pump is therefore recommended for the H2O2 process. Based on the complex nature of the heat recovery system, we anticipated that capital costs could make investments financially unattractive where steam costs are low, especially where co-generation is involved. We believe that the enhanced heat transfer equipment has the potential to significantly improve the performance of TEE crystallizers, independent of the absorption heat-pump recovery system. Where steam costs are high, more detailed design/cost engineering will be required to verify the economic viability of the technology. Due to the long payback period estimated for the TEE open system, further studies on the TEE system are not warranted unless there are significant future improvements to heat pump technology. For the H2O2 distillation cycle heat pump waste heat recovery system, there were no significant process constraints and the estimated 5 years payback period is encouraging. We therefore recommend further developments of application of the thermal heat pump in the H2O2 distillation process with the focus on the technical and economic viability of heat exchangers equipped with the state-of-the-art enhancements. This will require additional funding for a prototype unit to validate enhanced thermal performances of heat transfer equipment, evaluat

  19. Electrostatic coalescence of used automotive crankcase oil as an alternative to other separation processes

    E-Print Network [OSTI]

    Dixon, John Leslie

    1998-01-01T23:59:59.000Z

    , verified by separating and analyzing a used oil emulsion. The metal removal efficiency was compared to that of a five day gravity settling. Separation experiments were performed in a 2.26 L coalescer with a flat parallel insulated electrode configuration...

  20. Evolution of isotopic composition of reprocessed uranium during the multiple recycling in light water reactors with natural uranium feed

    SciTech Connect (OSTI)

    Smirnov, A. Yu., E-mail: a.y.smirnoff@rambler.ru; Sulaberidze, G. A. [National Research Nuclear University MEPhI (Russian Federation); Alekseev, P. N.; Dudnikov, A. A.; Nevinitsa, V. A., E-mail: neva@dhtp.kiae.ru; Proselkov, V. N.; Chibinyaev, A. V. [Russian Research Centre Kurchatov Institute (Russian Federation)

    2012-12-15T23:59:59.000Z

    A complex approach based on the consistent modeling of neutron-physics processes and processes of cascade separation of isotopes is applied for analyzing physical problems of the multiple usage of reprocessed uranium in the fuel cycle of light water reactors. A number of scenarios of multiple recycling of reprocessed uranium in light water reactors are considered. In the process, an excess absorption of neutrons by the {sup 236}U isotope is compensated by re-enrichment in the {sup 235}U isotope. Specific consumptions of natural uranium for re-enrichment of the reprocessed uranium depending on the content of the {sup 232}U isotope are obtained.

  1. Process for separation of zirconium-88, rubidium-83 and yttrium-88

    DOE Patents [OSTI]

    Heaton, Richard C. (Los Alamos, NM); Jamriska, Sr., David J. (Los Alamos, NM); Taylor, Wayne A. (Los Alamos, NM)

    1994-01-01T23:59:59.000Z

    A process for selective separation of strontium-82 and strontium-85 from proton irradiated molybdenum targets is provided and includes dissolving the molybdenum target in a hydrogen peroxide solution to form a first ion-containing solution, passing the first ion-containing solution through a first cationic resin whereby ions selected from the group consisting of molybdenum, niobium, technetium, selenium, vanadium, arsenic, germanium, zirconium and rubidium remain in the first ion-containing solution while ions selected from the group consisting of rubidium, zinc, beryllium, cobalt, iron, manganese, chromium, strontium, yttrium and zirconium are selectively adsorbed by the first resin, contacting the first resin with an acid solution capable of stripping adsorbed ions from the first cationic exchange resin whereby the adsorbed ions are removed from the first resin to form a second ion-containing solution, evaporating the second ion-containing solution for time sufficient to remove substantially all of the acid and water from the second ion-containing solution whereby a residue remains, dissolving the residue from the evaporated second-ion containing solution in a dilute acid to form a third ion-containing solution, said third ion-containing solution having an acid molarity adapted to permit said ions to be adsorbed by a cationic exchange resin, passing the third ion-containing solution through a second cationic resin whereby the ions are adsorbed by the second resin, contacting the second resin with a dilute sulfuric acid solution whereby the adsorbed ions selected from the group consisting of rubidium, zinc, beryllium, cobalt, iron, manganese, chromium, and zirconium are selectively removed from the second resin, and contacting the second resin with a dilute acid solution whereby the adsorbed strontium ions are selectively removed. Zirconium, rubidium, and yttrium radioisotopes can also be recovered with additional steps.

  2. Hillslope Hydrological Processes in a Costa Rican Rainforest: Water Supply Partitioning Using Isotope Tracers

    E-Print Network [OSTI]

    DuMont, Andrea Lyn

    2014-04-24T23:59:59.000Z

    Blancas Hydroelectric Project, and for improved predictions in similar, ungauged watersheds (ICE 2002). Study Watershed The study watershed is located in San Juan de Peñas Blancas, east of the Cordillera de Tilarán mountain range backing up... peaks. These goals were accomplished by supplementing hydraulic and physical data already available at the site with use of isotope tracers. Methods Study Site The 2.2 ha watershed used in this research is located in Peñas Blancas, Costa Rica...

  3. Hybrid membrane/cryogenic separation of oxygen from air for use in the oxy-fuel process

    E-Print Network [OSTI]

    Struchtrup, Henning

    in underground caverns, e.g., depleted oil or gas fields. The process of oxy-fuel combustion requires high purity-fuel combustion requires the separation of oxygen from air on a large scale for use in the combustion chamber Looping Combustion [6] are also proposed but still require significant development. Kvams- dal et al. [7

  4. 982 IEEE TRANSACTIONS ON IMAGE PROCESSING, VOL. 18, NO. 5, MAY 2009 Bayesian Separation of Images Modeled

    E-Print Network [OSTI]

    on a statistical model of the gradient image, and we use a fully Bayesian method with modified-Gibbs sam- pling. We982 IEEE TRANSACTIONS ON IMAGE PROCESSING, VOL. 18, NO. 5, MAY 2009 Bayesian Separation of Images fields within a Bayesian framework. The Bayesian for- mulation enables the incorporation of prior image

  5. The physical separation and recovery of metals from wastes. Process engineering for the chemical, metals and minerals industries, Volume 1

    SciTech Connect (OSTI)

    Veasey, T.J.; Wilson, R.J. (eds.) (Univ. of Birmingham (United Kingdom). School of Chemical Engineering); Squires, D.M. (ed.) (Newell Engineering Ltd., Redditch (United Kingdom))

    1993-01-01T23:59:59.000Z

    This book deals with the physical processes used for the separation of secondary metals from waste sources. The introduction briefly considers the history of the secondary metals industries, defines the terms used in materials recycling and discusses the potential for resource recovery and improved processing. A comprehensive survey is given of the unit operations employed for metals recovery and reclamation, and this is followed by detailed descriptions of processes used to treat fragmentized metal wastes and granulated metal wastes. The final chapter reviews the processing of urban wastes for metals recovery, and gives details of modern plant and practices. The volume aims to bring together technical information on metals recovery from a wide range of sources in order to give a unified review of an important engineering and environmental topic. Topics include: general definitions used in materials recycling; the potential for resource recovery; secondary metals; ranking of scrap; the potential for improved processing; comminution; physical separation methods; the scrap industry; automobile composition; shredders; non-magnetic processing; metal reclamation processes; waste tire processing; battery processing; thermal processing systems; composition of urban waste; and material recovery.

  6. Isotope and Nuclear Chemistry Division annual report, FY 1983

    SciTech Connect (OSTI)

    Heiken, J.H.; Lindberg, H.A. (eds.)

    1984-05-01T23:59:59.000Z

    This report describes progress in the major research and development programs carried out in FY 1983 by the Isotope and Nuclear Chemistry Division. It covers radiochemical diagnostics of weapons tests; weapons radiochemical diagnostics research and development; other unclassified weapons research; stable and radioactive isotope production, separation, and applications (including biomedical applications); element and isotope transport and fixation; actinide and transition metal chemistry; structural chemistry, spectroscopy, and applications; nuclear structure and reactions; irradiation facilities; advanced analytical techniques; development and applications; atmospheric chemistry and transport; and earth and planetary processes.

  7. The production of chemicals from food processing wastes using a novel fermenter separator. Annual progress report, January 1993--March 1994

    SciTech Connect (OSTI)

    Dale, M.C.; Venkatesh, K.V.; Choi, H.; Salicetti-Piazza, L.; Borgos-Rubio, N.; Okos, M.R.; Wankat, P.C.

    1994-03-15T23:59:59.000Z

    The basic objective of this project is to convert waste streams from the food processing industry to usable fuels and chemicals using novel bioreactors. These bioreactors should allow economical utilization of waste (whey, waste sugars, waste starch, bottling wastes, candy wastes, molasses, and cellulosic wastes) by the production of ethanol, acetone/butanol, organic acids (acetic, lactic, and gluconic), yeast diacetyl flavor, and antifungal compounds. Continuous processes incorporating various processing improvements such as simultaneous product separation and immobilized cells are being developed to allow commercial scale utilization of waste stream. The production of ethanol by a continuous reactor-separator is the process closest to commercialization with a 7,500 liter pilot plant presently sited at an Iowa site to convert whey lactose to ethanol. Accomplishments during 1993 include installation and start-up of a 7,500 liter ICRS for ethanol production at an industry site in Iowa; Donation and installation of a 200 liter yeast pilot Plant to the project from Kenyon Enterprises; Modeling and testing of a low energy system for recovery of ethanol from vapor is using a solvent absorption/extractive distillation system; Simultaneous saccharification/fermentation of raw corn grits and starch in a stirred reactor/separator; Testing of the ability of `koji` process to ferment raw corn grits in a `no-cook` process.

  8. Method for laser induced isotope enrichment

    DOE Patents [OSTI]

    Pronko, Peter P.; Vanrompay, Paul A.; Zhang, Zhiyu

    2004-09-07T23:59:59.000Z

    Methods for separating isotopes or chemical species of an element and causing enrichment of a desired isotope or chemical species of an element utilizing laser ablation plasmas to modify or fabricate a material containing such isotopes or chemical species are provided. This invention may be used for a wide variety of materials which contain elements having different isotopes or chemical species.

  9. Process for separation of CO/sub 2/ from CO/sub 2/-containing gases

    SciTech Connect (OSTI)

    Linde, G.

    1985-07-09T23:59:59.000Z

    For separating CO/sub 2/ from CO/sub 2/-containing gases, especially stack gases and/or blast furnace gases, dimethylformamide is employed as a physical scrubbing medium to ensure high CO/sub 2/ purity. After absorption of CO/sub 2/, the DMF is regenerated and returned into the scrubbing stage. Dimethylformamide is utilized as the scrubbing medium.

  10. The marine biogeochemistry of zinc isotopes

    E-Print Network [OSTI]

    John, Seth G

    2007-01-01T23:59:59.000Z

    Zinc (Zn) stable isotopes can record information about important oceanographic processes. This thesis presents data on Zn isotopes in anthropogenic materials, hydrothermal fluids and minerals, cultured marine phytoplankton, ...

  11. Supercritical fluid extraction of bitumen free solids separated from Athabasca oil sand feed and hot water process tailings pond sludge

    SciTech Connect (OSTI)

    Kotlyar, L.S.; Sparks, B.D.; Woods, J.R.; Ripmeester, J.A. (National Research Council of Canada, Ottawa, ON (Canada). Div. of Chemistry)

    1990-01-01T23:59:59.000Z

    The presence of strongly bound organic matter (SOM), in association with certain solids fractions, causes serious problems in the processability of Athabasca oil sands as well as in the settling and compaction of hot water process tailing pond sludge. It has been demonstrated that a substantial amount of this SOM can be separated from oil sands feed and sludge solids, after removal of bitumen by toluene, using a supercritical fluid extraction (SFE) method. The extracted material is soluble in common organic solvents which allows a direct comparison, between the SOM separated from oil sands and sludges, from the point of view of both gross analysis of the major compound types and detailed analysis of chemical structures.

  12. A calcium oxide sorbent process for bulk separation of carbon dioxide. Quarterly progress report No. 12, July 1992--September 1992

    SciTech Connect (OSTI)

    Harrison, D.P.

    1992-10-01T23:59:59.000Z

    Objective is to investigate the feasibility of a high-temperature, high-pressure process for bulk separation of CO{sub 2} from coal- derived gas. An electrobalance reactor was used in Phase I; in Phase II, the switch was made to a fixed-bed reactor with capability for feed and product gas analysis. A gas chromatograph was delivered, installed, and operator training carried out. The sampling valve sequence is discussed.

  13. A calcium oxide sorbent process for bulk separation of carbon dioxide. Quarterly progress report No. 9, January 1992--March 1992

    SciTech Connect (OSTI)

    Harrison, D.P.

    1992-04-01T23:59:59.000Z

    This research project is investigating the technical feasibility of a high-temperature, high-pressure process for the bulk separation of CO{sub 2} from coal-derived gas. Phase I consisted of 6 tasks. Phase II added a seventh task to the project. This report is limited to a description of the final experimental results obtained in Phase I, Task 5 (multicycle tests), and a brief overview of justification and plans for Phase II, Task 7.

  14. Isotope Trace Studies of Diffusion in Silicates and of Geological Transport Processes Using Actinide Elements

    SciTech Connect (OSTI)

    Prof. G. J. Wasserburg

    2001-01-19T23:59:59.000Z

    Over the past year we have competed two studies of Os concentration and isotopic composition in rivers from the Himalayan uplift and in hydrothermal fluids from the Juan de Fuca Ridge. Both of these studies have been published. We have completed a study of paleo-climate in Soreq Cave, Israel, and have expanded our studies of the transport of U-Th through riverine and estuarine environments. We are completing two studies of weathering and transport in the vadose in two very different environments--one a tropical regime with a deep laterite profile and the other a northern arboreal forest with only a thin weathering zone. We have begun a new study of U-Th in aquifers with low water velocity.

  15. Towards an electro-magnetic field separation of deposited material implemented in an ion beam sputter process

    SciTech Connect (OSTI)

    Malobabic, Sina; Jupe, Marco; Ristau, Detlev [Laser Component Department, Laser Zentrum Hannover e.V., Hollerithallee 8, 30149 Hannover (Germany) [Laser Component Department, Laser Zentrum Hannover e.V., Hollerithallee 8, 30149 Hannover (Germany); Quest: Centre of Quantum Engineering and Space-Time Research, Leibniz Universitaet Hannover, Hannover (Germany)

    2013-06-03T23:59:59.000Z

    Nowadays, Ion Beam Sputter (IBS) processes are very well optimized on an empirical basis. To achieve further progresses, a modification of the IBS process by guiding the coating material using an axial magnetic field and an additional electrical field has been studied. The electro-magnetic (EM) field leads to a significant change in plasma properties and deposition rate distributions, whereas an increase in deposition rate along the centerline of the axial EM field around 150% was observed. These fundamental studies on the prototype are the basis for the development of an applicable and workable design of a separation device.

  16. Process for producing fuel grade ethanol by continuous fermentation, solvent extraction and alcohol separation

    DOE Patents [OSTI]

    Tedder, Daniel W. (Marietta, GA)

    1985-05-14T23:59:59.000Z

    Alcohol substantially free of water is prepared by continuously fermenting a fermentable biomass feedstock in a fermentation unit, thereby forming an aqueous fermentation liquor containing alcohol and microorganisms. Continuously extracting a portion of alcohol from said fermentation liquor with an organic solvent system containing an extractant for said alcohol, thereby forming an alcohol-organic solvent extract phase and an aqueous raffinate. Said alcohol is separated from said alcohol-organic solvent phase. A raffinate comprising microorganisms and unextracted alcohol is returned to the fermentation unit.

  17. Factors Controlling Redox Speciation of Plutonium and Neptunium in Extraction Separation Processes

    SciTech Connect (OSTI)

    Paulenova, Alena [Principal Investigator; Vandegrift, III, George F. [Collaborator

    2013-09-24T23:59:59.000Z

    The objective of the project was to examine the factors controlling redox speciation of plutonium and neptunium in UREX+ extraction in terms of redox potentials, redox mechanism, kinetics and thermodynamics. Researchers employed redox-speciation extractions schemes in parallel to the spectroscopic experiments. The resulting distribution of redox species w studied uring spectroscopic, electrochemical, and spectro-electrochemical methods. This work reulted in collection of data on redox stability and distribution of redox couples in the nitric acid/nitrate electrolyte and the development of redox buffers to stabilize the desired oxidation state of separated radionuclides. The effects of temperature and concentrations on the redox behavior of neptunium were evaluated.

  18. Pressure drop in cyclone separators commonly used in the agricultural processing industry

    E-Print Network [OSTI]

    Guzman, Francisco Alejandro

    1984-01-01T23:59:59.000Z

    -20, 406 mm diameter cyclone. 58 sion of kinetic energy into static and in some cases flow separation. A comparison between the static pressure at the piezometer ring and at the cyclone inlet as shown in Tables 7 and 8 (pp. 41 and 42) seemed... and so small in magnitude that for graphical purposes they were assumed to be zero. Examination of the static pressures in Tables 9 and 10 (pp. 43 and 44) suggested a regain of static pressure at the cyclone inlets. For instance, at an airflow rate...

  19. Adsorption/Membrane Filtration as a Contaminant Concentration and Separation Process for Mixed Wastes and Tank Wastes - Final Report

    SciTech Connect (OSTI)

    Benjamin, M.M.

    1999-10-01T23:59:59.000Z

    This project was conducted to evaluate novel approaches for removing radioactive strontium (Sr) and cesium (Cs) from the tank wastes. The bulk of the Sr removal research conducted as part of this project investigated adsorption of Sr onto a novel adsorbent known as iron-oxide-coated sand. The second major focus of the work was on the removal of cesium. Since the chemistries of strontium and cesium have little commonality, different materials (namely, cesium scavengers known as hexacyanoferrates, HCFs) were employed in these tests. This study bridged several scientific areas and yielded valuable knowledge for implementing new technological processes. The applicability of the results extends beyond the highly specialized application niches investigated experimentally to other issues of potential interest for EMSP programs (e.g., separation of chromium from a variety of wastes using IOCS, separation of Cs from neutral and acidic wastes with EC-controlled HCFs).

  20. Composition and process for separating cesium ions from an acidic aqueous solution also containing other ions

    DOE Patents [OSTI]

    Dietz, M.L.; Horwitz, E.P.; Bartsch, R.A.; Barrans, R.E. Jr.; Rausch, D.

    1999-03-30T23:59:59.000Z

    A crown ether cesium ion extractant is disclosed as is its synthesis. The crown ether cesium ion extractant is useful for the selective purification of cesium ions from aqueous acidic media, and more particularly useful for the isolation of radioactive cesium-137 from nuclear waste streams. Processes for isolating cesium ions from aqueous acidic media using the crown ether cesium extractant are disclosed as are processes for recycling the crown ether cesium extractant and processes for recovering cesium from a crown ether cesium extractant solution. 4 figs.

  1. Composition and process for separating cesium ions from an acidic aqueous solution also containing other ions

    DOE Patents [OSTI]

    Dietz, Mark L. (Elmhurst, IL); Horwitz, E. Philip (Naperville, IL); Bartsch, Richard A. (Lubbock, TX); Barrans, Jr., Richard E. (Downers Grove, IL); Rausch, David (Naperville, IL)

    1999-01-01T23:59:59.000Z

    A crown ether cesium ion extractant is disclosed as is its synthesis. The crown ether cesium ion extractant is useful for the selective purification of cesium ions from aqueous acidic media, and more particularly useful for the isolation of radioactive cesium-137 from nuclear waste streams. Processes for isolating cesium ions from aqueous acidic media using the crown ether cesium extractant are disclosed as are processes for recycling the crown ether cesium extractant and processes for recovering cesium from a crown ether cesium extractant solution.

  2. RESEARCH AND DEVELOPMENT OF AN INTEGRAL SEPARATOR FOR A CENTRIFUGAL GAS PROCESSING FACILITY

    SciTech Connect (OSTI)

    LANCE HAYS

    2007-02-27T23:59:59.000Z

    A COMPACT GAS PROCESSING DEVICE WAS INVESTIGATED TO INCREASE GAS PRODUCTION FROM REMOTE, PREVIOUSLY UN-ECONOMIC RESOURCES. THE UNIT WAS TESTED ON AIR AND WATER AND WITH NATURAL GAS AND LIQUID. RESULTS ARE REPORTED WITH RECOMMENDATIONS FOR FUTURE WORK.

  3. Freeze Crystallization: Improving the Energy Efficiency of a Low-Energy Separation Process

    E-Print Network [OSTI]

    Heist, J. A.

    1981-01-01T23:59:59.000Z

    load reductions. Pulp and Paper Mills - This industry has both large quantities of waste heat and large flows of process fluids. The most concentrated of the streams, black liquor from digestion of the lignin in the wood, is concentrated...

  4. On-line method of determining utilization factor in Hg-196 photochemical separation process

    DOE Patents [OSTI]

    Grossman, Mark W. (Belmont, MA); Moskowitz, Philip E. (Peabody, MA)

    1992-01-01T23:59:59.000Z

    The present invention is directed to a method for determining the utilization factor [U] in a photochemical mercury enrichment process (.sup.196 Hg) by measuring relative .sup.196 Hg densities using absorption spectroscopy.

  5. THE MULTI-ISOTOPE PROCESS (MIP) MONITOR: A NEAR-REAL-TIME, NON-DESTRUCTIVE, INDICATOR OF SPENT NUCLEAR FUEL REPROCESSING CONDITIONS

    SciTech Connect (OSTI)

    Schwantes, Jon M.; Orton, Christopher R.; Fraga, Carlos G.; Douglas, Matthew; Christensen, Richard

    2010-05-07T23:59:59.000Z

    Researchers from Pacific Northwest National Laboratory and The Ohio State University are working to develop a system for monitoring spent nuclear fuel reprocessing facilities on-line, non-destructively, and in near-real-time. This method, known as the Multi-Isotope Process (MIP) Monitor, is based upon the measurement of distribution patterns of a suite of indicator (radioactive) isotopes present within product and waste streams of a nuclear reprocessing facility. Signatures from these indicator isotopes are monitored on-line by gamma spectrometry and compared, in near-real-time, to patterns representing "normal" process conditions using multivariate pattern recognition software. By targeting gamma-emitting indicator isotopes, the MIP Monitor approach is compatible with the use of small, portable, high-resolution gamma detectors that may be easily deployed throughout an existing facility. In addition, utilization of a suite of radio-elements, including ones with multiple oxidation states, increases the likelihood that attempts to divert material via process manipulation would be detected. Proof-of-principle modeling exercises simulating changes in acid strength have been completed and the results are promising. Laboratory validation is currently under way and significant results are available. The latest experimental results, along with an overview of the method will be presented.

  6. MONITORING SPENT NUCLEAR FUEL REPROCESSING CONDITIONS NON-DESTRUCTIVELY AND IN NEAR-REAL-TIME USING THE MULTI-ISOTOPE PROCESS (MIP) MONITOR

    SciTech Connect (OSTI)

    Orton, Christopher R.; Fraga, Carlos G.; Douglas, Matthew; Christensen, Richard; Schwantes, Jon M.

    2010-05-07T23:59:59.000Z

    Researchers from Pacific Northwest National Laboratory and The Ohio State University are working to develop a system for monitoring spent nuclear fuel reprocessing facilities on-line, nondestructively, and in near-real-time. This method, known as the Multi-Isotope Process (MIP) Monitor, is based upon the measurement of distribution patterns of a suite of indicator (radioactive) isotopes present within product and waste streams of a nuclear reprocessing facility. Signatures from these indicator isotopes are monitored on-line by gamma spectrometry and compared, in near-real-time, to patterns representing "normal" process conditions using multivariate pattern recognition software. By targeting gamma-emitting indicator isotopes, the MIP Monitor approach is compatible with the use of small, portable, high-resolution gamma detectors that may be easily deployed throughout an existing facility. In addition, utilization of a suite of radio-elements, including ones with multiple oxidation states, increases the likelihood that attempts to divert material via process manipulation would be detected. Proof-of-principle modeling exercises simulating changes in acid strength have been completed and the results are promising. Laboratory testing is currently under way and significant results are available. Recent experimental results, along with an overview of the method are presented.

  7. Measurement of the Europium Isotope Ratio for the Extremely Metal-Poor, r-Process-Enhanced Star CS31082-001

    E-Print Network [OSTI]

    W. Aoki; S. Honda; T. C. Beers; C. Sneden

    2002-11-28T23:59:59.000Z

    We report the first measurement of the isotope fraction of europium (151Eu and 153Eu) for the extremely metal-poor, r-process-enhanced star CS31082-001, based on high-resolution spectra obtained with the Subaru Telescope High Dispersion Spectrograph. We have also obtained new measurements of this ratio for two similar stars with previous europium isotope measurements, CS22892-052 and HD115444. The measurements were made using observations of the Eu lines in these spectra that are most significantly affected by isotope shifts and hyperfine splitting. The fractions of 151Eu derived for CS31082-001, CS22892-052, and HD115444 are 0.44, 0.51, and 0.46, respectively, with uncertainties of about +/-0.1. CS31082-001, the first star with a meaningful measurement of U outside of the solar system, is known to exhibit peculiar abundance ratios between the actinide and rare-earth elements (e.g., Th/Eu), ratios that are significantly different from those for other stars with large excesses of r-process elements, such as our two comparison objects. Nevertheless, our analysis indicates that the Eu isotope ratio of CS31082-001 agrees, within the errors, with those of other r-process-enhanced objects, and with that of solar-system material.

  8. Optimal synthesis of p-xylene separation processes based on crystallization technology

    E-Print Network [OSTI]

    Grossmann, Ignacio E.

    that arises in hybrid designs where the first step is commonly performed by adsorption. A novel superstructure) adsorption, or (3) a hybrid crystallization/adsorption process.1 Distillation is not a competitive technology) resulting in columns with high reflux ratios and a large number of trays. Table 1 Adsorption

  9. Membrane separation of solids from corn processing streams Tricia L. Templin a,1

    E-Print Network [OSTI]

    ) 1536­1545 #12;requiring use of scrubbers and thermal oxidizers; exposure of coproducts to heat can are characterized by high water content. Removal of water and recovery of solids are major economic and logistical. Ultrafiltration of STW and SKW had little effect on water removal or solids recovery. Corn was processed

  10. Technical Report: Investigation of Carbon Cycle Processes within a Managed Landscape: An Ecosystem Manipulation and Isotope Tracer Approach

    SciTech Connect (OSTI)

    Griffis, Timothy J; Baker, John M; Billmark, Kaycie

    2009-06-01T23:59:59.000Z

    The goal of this research is to provide a better scientific understanding of carbon cycle processes within an agricultural landscape characteristic of the Upper Midwest. This project recognizes the need to study processes at multiple spatial and temporal scales to reduce uncertainty in ecosystem and landscape-scale carbon budgets to provide a sound basis for shaping future policy related to carbon management. Specifically, this project has attempted to answer the following questions: 1. Would the use of cover crops result in a shift from carbon neutral to significant carbon gain in corn-soybean rotation ecosystems of the Upper Midwest? 2. Can stable carbon isotope analyses be used to partition ecosystem respiration into its autotrophic and heterotrophic components? 3. Can this partitioning be used to better understand the fate of crop residues to project changes in the soil carbon reservoir? 4. Are agricultural ecosystems of the Upper Midwest carbon neutral, sinks, or sources? Can the proposed measurement and modeling framework help address landscape-scale carbon budget uncertainties and help guide future carbon management policy?

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

    DOE Patents [OSTI]

    Tsai, S.P.

    1997-07-08T23:59:59.000Z

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

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

    DOE Patents [OSTI]

    Tsai, Shih-Perng (Naperville, IL)

    1997-01-01T23:59:59.000Z

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

  13. On the origin of the lightest Molybdenum isotopes

    E-Print Network [OSTI]

    Jacob Lund Fisker; Robert D. Hoffman; Jason Pruet

    2009-01-15T23:59:59.000Z

    We discuss implications of recent precision measurements for the Rh93 proton separation energy for the production of the lightest molybdenum isotopes in proton-rich type II supernova ejecta. It has recently been shown that a novel neutrino-induced process makes these ejecta a promising site for the production of the light molybdenum isotopes and other "p-nuclei" with atomic mass near 100. The origin of these isotopes has long been uncertain. A distinguishing feature of nucleosynthesis in neutrino-irradiated outflows is that the relative production of Mo92 and Mo94 is set by a competition governed by the proton separation energy of Rh93. We use detailed nuclear network calculations and the recent experimental results for this proton separation energy to place constraints on the outflow characteristics that produce the lightest molybdenum isotopes in their solar proportions. It is found that for the conditions calculated in recent two-dimensional supernova simulations, and also for a large range of outflow characteristics around these conditions, the solar ratio of Mo92 to Mo94 cannot be achieved. This suggests that either proton-rich winds from type II supernova do not exclusively produce both isotopes, or that these winds are qualitatively different than calculated in today's supernova models.

  14. Report of Separate Effects Testing for Modeling of Metallic Fuel Casting Process

    SciTech Connect (OSTI)

    Crapps, Justin M. [Los Alamos National Laboratory; Galloway, Jack D. [Los Alamos National Laboratory; Decroix, David S. [Los Alamos National Laboratory; Korzekwa, David A. [Los Alamos National Laboratory; Aikin, Robert M. Jr. [Los Alamos National Laboratory; Unal, Cetin [Los Alamos National Laboratory; Fielding, R. [Idaho National Laboratory; Kennedy, R [Idaho National Laboratory

    2012-06-29T23:59:59.000Z

    In order to give guidance regarding the best investment of time and effort in experimental determination of parameters defining the casting process, a Flow-3D model of the casting process was used to investigate the most influential parameters regarding void fraction of the solidified rods and solidification speed for fluid flow parameters, liquid heat transfer parameters, and solid heat transfer parameters. Table 1 summarizes the most significant variables for each of the situations studied. A primary, secondary, and tertiary effect is provided for fluid flow parameters (impacts void fraction) and liquid heat transfer parameters (impacts solidification). In Table 1, the wetting angle represents the angle between the liquid and mold surface as pictured in Figure 1. The viscosity is the dynamic viscosity of the liquid and the surface tension is the property of the surface of a liquid that allows it to resist an external force. When only considering solid heat transfer properties, the variations from case to case were very small. Details on this conclusion are provided in the section considering solid heat transfer properties. The primary recommendation of the study is to measure the fluid flow parameters, specifically the wetting angle, surface tension, and dynamic viscosity, in order of importance, as well as the heat transfer parameters latent heat and specific heat of the liquid alloy. The wetting angle and surface tension can be measured simultaneously using the sessile drop method. It is unclear whether there is a temperature dependency in these properties. Thus measurements for all three parameters are requested at 1340, 1420, and 1500 degrees Celsius, which correspond to the minimum, middle, and maximum temperatures of the liquid alloy during the process. In addition, the heat transfer coefficient between the mold and liquid metal, the latent heat of transformation, and the specific heat of the liquid metal all have strong influences on solidification. These parameters should be measured to achieve better simulation fidelity. Information on all the mentioned parameters is virtually nonexistent. Presently, all the parameters within the casting model are estimates based on pure U, or another alloy such as U-Ni.

  15. Apparatus and process for the separation of hydrophobic and hydrophilic particles using microbubble column flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, Roe-Hoan (Blacksburg, VA); Adel, Gregory T. (Blacksburg, VA); Luttrell, Gerald H. (Blacksburg, VA)

    1992-01-01T23:59:59.000Z

    A method and apparatus are disclosed for the microbubble flotation separation of very fine and coarse particles, especially coal and minerals, so as to produce high purity and high recovery efficiency. This is accomplished through the use of a flotation column, microbubbles, recycling of the flotation pulp, and countercurrent wash water to gently wash the froth. Also disclosed are unique processes and apparatus for generating microbubbles for flotation in a highly efficient and inexpensive manner using either a porous tube or in-line static generators.

  16. Apparatus and process for the separation of hydrophobic and hydrophilic particles using microbubble column flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, Roe-Hoan (Blacksburg, VA); Adel, Gregory T. (Blacksburg, VA); Luttrell, Gerald H. (Blacksburg, VA)

    1998-01-01T23:59:59.000Z

    A method and apparatus are disclosed for the microbubble flotation separation of very fine and coarse particles, especially coal and minerals, so as to produce high purity and high recovery efficiency. This is accomplished through the use of a flotation column, microbubbles, recycling of the flotation pulp, and countercurrent wash water to gently wash the froth. Also disclosed are unique processes and apparatus for generating microbubbles for flotation in a highly efficient and inexpensive manner using either a porous tube or in-line static generators.

  17. Apparatus and process for the separation of hydrophobic and hydrophilic particles using microbubble column flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, R.H.; Adel, G.T.; Luttrell, G.H.

    1998-09-29T23:59:59.000Z

    A method and apparatus are disclosed for the microbubble flotation separation of very fine and coarse particles, especially coal and minerals, so as to produce high purity and high recovery efficiency. This is accomplished through the use of a flotation column, microbubbles, recycling of the flotation pulp, and countercurrent wash water to gently wash the froth. Also disclosed are unique processes and apparatus for generating microbubbles for flotation in a highly efficient and inexpensive manner using either a porous tube or in-line static generators. 14 figs.

  18. Apparatus and process for the separation of hydrophobic and hydrophilic particles using microbubble column flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, R.H.; Adel, G.T.; Luttrell, G.H.

    1992-12-01T23:59:59.000Z

    A method and apparatus are disclosed for the microbubble flotation separation of very fine and coarse particles, especially coal and minerals, so as to produce high purity and high recovery efficiency. This is accomplished through the use of a flotation column, microbubbles, recycling of the flotation pulp, and countercurrent wash water to gently wash the froth. Also disclosed are unique processes and apparatus for generating microbubbles for flotation in a highly efficient and inexpensive manner using either a porous tube or in-line static generators. 14 figs.

  19. Advanced Membrane Separation Technologies for Energy Recovery from Industrial Process Streams

    SciTech Connect (OSTI)

    Keiser, J.R.; Wang, D. (Gas Technology Institute); Bischoff, B.; Ciora (Media and Process Technology); Radhakrishnan, B.; Gorti, S.B.

    2013-01-14T23:59:59.000Z

    Recovery of energy from relatively low-temperature waste streams is a goal that has not been achieved on any large scale. Heat exchangers do not operate efficiently with low-temperature streams and thus require such large heat exchanger surface areas that they are not practical. Condensing economizers offer one option for heat recovery from such streams, but they have not been widely implemented by industry. A promising alternative to these heat exchangers and economizers is a prototype ceramic membrane system using transport membrane technology for separation of water vapor and recovery of heat. This system was successfully tested by the Gas Technology Institute (GTI) on a natural gas fired boiler where the flue gas is relatively clean and free of contaminants. However, since the tubes of the prototype system were constructed of aluminum oxide, the brittle nature of the tubes limited the robustness of the system and even limited the length of tubes that could be used. In order to improve the robustness of the membrane tubes and make the system more suitable for industrial applications, this project was initiated with the objective of developing a system with materials that would permit the system to function successfully on a larger scale and in contaminated and potentially corrosive industrial environments. This required identifying likely industrial environments and the hazards associated with those environments. Based on the hazardous components in these environments, candidate metallic materials were identified that are expected to have sufficient strength, thermal conductivity and corrosion resistance to permit production of longer tubes that could function in the industrial environments identified. Tests were conducted to determine the corrosion resistance of these candidate alloys, and the feasibility of forming these materials into porous substrates was assessed. Once the most promising metallic materials were identified, the ability to form an alumina membrane layer on the surface of the metallic tubes was evaluated. Evaluation of this new style of membrane tube involved exposure to SO{sub 2} containing gases as well as to materials with a potential for fouling. Once the choice of substrate and membrane materials and design were confirmed, about 150 tubes were fabricated and assembled into three modules. These modules were mounted on an industrial size boiler and their performance carefully monitored during a limited testing period. The positive results of this performance test confirm the feasibility of utilizing such a system for recovery of heat and water from industrial waste streams. The improved module design along with use of long metallic substrate tubes with a ceramic membrane on the outer surface resulted in the successful, limited scale demonstration of the Transport Membrane Condenser (TMC) technology in the GTI test facility. This test showed this technology can successfully recover a significant amount of heat and water from gaseous waste streams. However, before industry will make the investment to install a full scale TMC, a full scale system will need to be constructed, installed and successfully operated at a few industrial sites. Companies were identified that had an interest in serving as a host site for a demonstration system.

  20. Continuous flow system for controlling phases separation near ? transition

    SciTech Connect (OSTI)

    Chorowski, M.; Poli?ski, J. [Wroc?aw University of Technology, Wybrze?e Wyspia?skiego 27,50-560 Wroc?aw (Poland); Kempi?ski, W.; Trybu?a, Z.; ?o?, Sz. [Institute of Molecular Physics, Polish Academy of Sciences, ul. Smoluchowskiego 17,60-179 Pozna? (Poland); Cho?ast, K.; Kociemba, A. [Polish Oil and Gas Company, Odolanow, ul. Krotoszynska 148, 63-430 Odolanow (Poland)

    2014-01-29T23:59:59.000Z

    As demands on 3He are increasing and conventional 3He production through tritium decay is decreasing, alternative 3He production methods are becoming economically viable. One such possibility is to use entropy filters for extraction of the 3He isotope from natural gas. According to the phase diagram of the 3He, its solidification is impossible by only lowering of the temperature. Hence during the cooling process at stable pressure we can reach ?-point and pass to the special phase - He II. The total density of HeII is a sum of the two phases: normal the superfluid ones. It is possible to separate these two phases with an entropy filter - the barrier for the classically-behaving normal phase. This barrier can also be used to separate the two main isotopes of He: 4He and 3He, because at temperatures close to the 4He-?-point the 3He isotope is part of the normal phase. The paper presents continuous flow schemes of different separation methods of 3He from helium commodity coming from natural gas cryogenic processing. An overall thermodynamic efficiency of the 3He/4He separation process is presented. A simplified model of continuous flow HeI -HeII recuperative heat exchanger is given. Ceramic and carbon porous plugs have been tested in entropy filter applications.

  1. Separation Processes, Second Edition

    E-Print Network [OSTI]

    King, C. Judson

    1980-01-01T23:59:59.000Z

    of the hexafluoride, since UF6 is one of the few gaseousof flow. If a stream of UF6 containing 0.71% 235UF6, thesize needed for Knudsen flow, UF6 permeation rates are very

  2. Separation Processes, Second Edition

    E-Print Network [OSTI]

    King, C. Judson

    1980-01-01T23:59:59.000Z

    those discussed for staged contac- tors in Chap. 10. Stockarliquid and liquid- liquid contac- tors are reported by Perry

  3. REVISED FINAL REPORT – INDEPENDENT VERIFICATION SURVEY ACTIVITIES AT THE SEPARATIONS PROCESS RESEARCH UNIT SITES, NISKAYUNA, NEW YORK – DCN 0496-SR-06-1

    SciTech Connect (OSTI)

    Evan Harpenau

    2011-10-10T23:59:59.000Z

    The Separations Process Research Unit (SPRU) complex located on the Knolls Atomic Power Laboratory (KAPL) site in Niskayuna, New York, was constructed in the late 1940s to research the chemical separation of plutonium and uranium (Figure A-1). SPRU operated as a laboratory scale research facility between February 1950 and October 1953. The research activities ceased following the successful development of the reduction oxidation and plutonium/uranium extraction processes. The oxidation and extraction processes were subsequently developed for large scale use by the Hanford and Savannah River sites (aRc 2008a). Decommissioning of the SPRU facilities began in October 1953 and continued through the 1990s.

  4. Fabrication of Pd/Pd-Alloy Films by Surfactant Induced Electroless Plating for Hydrogen Separation from Advanced Coal Gasification Processes

    SciTech Connect (OSTI)

    Ilias, Shamsuddin; Kumar, Dhananjay

    2012-07-31T23:59:59.000Z

    Dense Pd, Pd-Cu and Pd-Ag composite membranes on microporous stainless steel substrate (MPSS) were fabricated by a novel electroless plating (EP) process. In the conventional Pd-EP process, the oxidation-reduction reactions between Pd-complex and hydrazine result in an evolution of NH{sub 3} and N{sub 2} gas bubbles. When adhered to the substrate surface and in the pores, these gas bubbles hinder uniform Pd-film deposition which results in dendrite growth leading to poor film formation. This problem was addressed by introducing cationic surfactant in the electroless plating process known as surfactant induced electroless plating (SIEP). The unique features of this innovation provide control of Pd-deposition rate, and Pd-grain size distribution. The surfactant molecules play an important role in the EP process by tailoring grain size and the process of agglomeration by removing tiny gas bubbles through adsorption at the gas-liquid interface. As a result surfactant can tailor a nanocrystalline Pd, Cu and Ag deposition in the film resulting in reduced membrane film thickness. Also, it produces a uniform, agglomerated film structure. The Pd-Cu and Pd-Ag membranes on MPSS support were fabricated by sequential deposition using SIEP method. The pre- and post-annealing characterizations of these membranes (Pd, Pd-Cu and Pd-Ag on MPSS substrate) were carried out by SEM, EDX, XRD, and AFM studies. The SEM images show significant improvement of the membrane surface morphology, in terms of metal grain structures and grain agglomeration compared to the membranes fabricated by conventional EP process. The SEM images and helium gas-tightness studies indicate that dense and thinner films of Pd, Pd-Cu and Pd-Ag membranes can be produced with shorter deposition time using surfactant. H{sub 2} Flux through the membranes fabricated by SIEP shows large improvement compared to those by CEP with comparable permselectivity. Pd-MPSS composite membrane was subjected to test for long term performance and thermal cycling (573 - 723 - 573 K) at 15 psi pressure drop for 1200 hours. Pd membranes showed excellent hydrogen permeability and thermal stability during the operational period. Under thermal cycling (573 K - 873 K - 573 K), Pd-Cu-MPSS membrane was stable and retained hydrogen permeation characteristics for over three months of operation. From this limited study, we conclude that SIEP is viable method for fabrication of defect-free, robust Pd-alloy membranes for high-temperature H{sub 2}-separation applications.

  5. Scandium separation from tungsten crucibles : preliminary investigation into the separation of scandium metal from tungsten metal crucibles using an acid soak process.

    SciTech Connect (OSTI)

    Boyle, Timothy J.; Hess, Ryan Falcone; Neville, Michael Luke; Howard, Panit Clifton

    2013-02-01T23:59:59.000Z

    The first step in an attempt to isolate Sco from a Wo crucible was explored by soaking the samples in a series of organic (HOAc) and inorganic (HCl, H2SO4, H3PO4, HNO3) acids. All samples, except the HOAc, yielded a powder. The weight loss suggests that HNO3 is the most efficient solvent; however, the powders were tentatively identified by PXRD and found to contain both W and Sc by-products. The higher weight loss may also indicate dissolution of the Wo crucible, which was further evidenced upon visual inspection of the crucible. The H3PO4 acid soak yielded the cleanest removal of Sc from the crucible. More work to understand the separation of the Sco from the Wo crucible is necessary but the acid routes appear to hold promise under not as of yet established criteria.

  6. Europium Isotope Ratios in s-Process-Element-Enhanced, Metal-Poor Stars: A New Probe of the 151Sm Branching

    E-Print Network [OSTI]

    Wako Aoki; Sean G. Ryan; Nobuyuki Iwamoto; Timothy C. Beers; John E. Norris; Hiroyasu Ando; Toshitaka Kajino; Grant J. Mathews; Masayuki Y. Fujimoto

    2003-06-26T23:59:59.000Z

    We report on the first measurement of the Eu isotope fractions (151Eu and 153Eu) in s-process-element-enhanced, metal-poor stars. We use these ratios to investigate the 151Sm branching of s-process nucleosynthesis. The measurement was made by detailed study of Eu II lines that are significantly affected by hyperfine splitting and isotope shifts in spectra of the carbon-rich, very metal-poor stars LP625-44 and CS31062-050, observed with the Subaru Telescope High Dispersion Spectrograph. The 151Eu fractions [fr(151Eu) = 151Eu/(151Eu+153Eu)] derived for LP625-44 and CS31062-050 are 0.60 and 0.55, respectively, with uncertainties of about +/- 0.05. These values are higher than found in solar-system material, but agree well with the predictions of recent s-process models. We derive new constraints on the temperature and neutron density during the s-process based on calculations of pulsed s-process models for the 151Eu fraction.

  7. TUNGSTEN ISOTOPIC COMPOSITIONS IN STARDUST SiC GRAINS FROM THE MURCHISON METEORITE: CONSTRAINTS ON THE s-PROCESS IN THE Hf-Ta-W-Re-Os REGION

    SciTech Connect (OSTI)

    Avila, Janaina N.; Ireland, Trevor R.; Holden, Peter [Research School of Earth Sciences, Australian National University, Canberra, ACT 0200 (Australia); Lugaro, Maria; Buntain, Joelene [Centre for Stellar and Planetary Astrophysics, Monash University, Clayton, VIC 3800 (Australia); Gyngard, Frank; Zinner, Ernst; Amari, Sachiko [Laboratory for Space Sciences and the Department of Physics, Washington University, One Brookings Drive, St. Louis, MO 63130 (United States); Cristallo, Sergio [Departamento de Fisica Teorica y del Cosmos, Universidad de Granada, Granada 18071 (Spain); Karakas, Amanda, E-mail: janaina.avila@anu.edu.au [Mount Stromlo Observatory, Australian National University, Weston Creek, ACT 2611 (Australia)

    2012-01-01T23:59:59.000Z

    We report the first tungsten isotopic measurements in stardust silicon carbide (SiC) grains recovered from the Murchison carbonaceous chondrite. The isotopes {sup 182,183,184,186}W and {sup 179,180}Hf were measured on both an aggregate (KJB fraction) and single stardust SiC grains (LS+LU fraction) believed to have condensed in the outflows of low-mass carbon-rich asymptotic giant branch (AGB) stars with close-to-solar metallicity. The SiC aggregate shows small deviations from terrestrial (= solar) composition in the {sup 182}W/{sup 184}W and {sup 183}W/{sup 184}W ratios, with deficits in {sup 182}W and {sup 183}W with respect to {sup 184}W. The {sup 186}W/{sup 184}W ratio, however, shows no apparent deviation from the solar value. Tungsten isotopic measurements in single mainstream stardust SiC grains revealed lower than solar {sup 182}W/{sup 184}W, {sup 183}W/{sup 184}W, and {sup 186}W/{sup 184}W ratios. We have compared the SiC data with theoretical predictions of the evolution of W isotopic ratios in the envelopes of AGB stars. These ratios are affected by the slow neutron-capture process and match the SiC data regarding their {sup 182}W/{sup 184}W, {sup 183}W/{sup 184}W, and {sup 179}Hf/{sup 180}Hf isotopic compositions, although a small adjustment in the s-process production of {sup 183}W is needed in order to have a better agreement between the SiC data and model predictions. The models cannot explain the {sup 186}W/{sup 184}W ratios observed in the SiC grains, even when the current {sup 185}W neutron-capture cross section is increased by a factor of two. Further study is required to better assess how model uncertainties (e.g., the formation of the {sup 13}C neutron source, the mass-loss law, the modeling of the third dredge-up, and the efficiency of the {sup 22}Ne neutron source) may affect current s-process predictions.

  8. Process for separating dissolved solids from a liquid using an anti-solvent and multiple effect evaporators

    DOE Patents [OSTI]

    Daniels, Edward J. (Oak Lawn, IL); Jody, Bassam J. (Chicago, IL); Bonsignore, Patrick V. (Channahon, IL)

    1994-01-01T23:59:59.000Z

    A process and system for treating aluminum salt cake containing water soluble halide salts by contacting the salt cake with water to dissolve water soluble halide salts forming a saturated brine solution. Transporting a portion of about 25% of the saturated brine solution to a reactor and introducing into the saturated brine solution at least an equal volume of a water-miscible low-boiling organic material such as acetone to precipitate a portion of the dissolved halide salts forming a three-phase mixture of an aqueous-organic-salt solution phase and a precipitated salt phase and an organic rich phase. The precipitated salt phase is separated from the other phases and the organic rich phase is recycled to the reactor. The remainder of the saturated brine solution is sent to a multiple effect evaporator having a plurality of stages with the last stage thereof producing low grade steam which is used to boil off the organic portion of the solution which is recycled.

  9. Process for separating dissolved solids from a liquid using an anti-solvent and multiple effect evaporators

    DOE Patents [OSTI]

    Daniels, E.J.; Jody, B.J.; Bonsignore, P.V.

    1994-07-19T23:59:59.000Z

    A process and system are disclosed for treating aluminum salt cake containing water soluble halide salts by contacting the salt cake with water to dissolve water soluble halide salts forming a saturated brine solution. Transporting a portion of about 25% of the saturated brine solution to a reactor and introducing into the saturated brine solution at least an equal volume of a water-miscible low-boiling organic material such as acetone to precipitate a portion of the dissolved halide salts forming a three-phase mixture of an aqueous-organic-salt solution phase and a precipitated salt phase and an organic rich phase. The precipitated salt phase is separated from the other phases and the organic rich phase is recycled to the reactor. The remainder of the saturated brine solution is sent to a multiple effect evaporator having a plurality of stages with the last stage thereof producing low grade steam which is used to boil off the organic portion of the solution which is recycled. 3 figs.

  10. INDEPENDENT TECHNICAL ASSESSMENT OF MANAGEMENT OF STORMWATER AND WASTEWATER AT THE SEPARATIONS PROCESS RESEARCH UNIT (SPRU) DISPOSITION PROJECT, NEW YORK

    SciTech Connect (OSTI)

    Abitz, R.; Jackson, D.; Eddy-Dilek, C.

    2011-06-27T23:59:59.000Z

    The U.S. Department of Energy (DOE) is currently evaluating the water management procedures at the Separations Process Research Unit (SPRU). The facility has three issues related to water management that require technical assistance: (1) due to a excessive rainfall event in October, 2010, contaminated water collected in basements of G2 and H2 buildings. As a result of this event, the contractor has had to collect and dispose of water offsite; (2) The failure of a sump pump at a KAPL outfall resulted in a Notice of Violation issued by the New York State Department of Environment and Conservation (NYSDEC) and subsequent Consent Order. On-site water now requires treatment and off-site disposition; and (3) stormwater infiltration has resulted in Strontium-90 levels discharged to the storm drains that exceed NR standards. The contractor has indicated that water management at SPRU requires major staff resources (at least 50 persons). The purpose of this review is to determine if the contractor's technical approach warrants the large number of staff resources and to ensure that the technical approach is compliant and in accordance with federal, state and NR requirements.

  11. Stable isotope fractionation by thermal diffusion through partially molten wet and dry silicate rocks

    E-Print Network [OSTI]

    Bindeman, Ilya N.

    isotope redistribution by thermal diffusion leading to enrichment of light isotopes at the hot endStable isotope fractionation by thermal diffusion through partially molten wet and dry silicate 2012 Editor: T.M. Harrison Keywords: thermal diffusion hydrogen isotope separation oxygen isotopes

  12. Isotope tracer studies of diffusion in silicates and of geological transport processes in aqueous systems using actinide elements

    SciTech Connect (OSTI)

    Wasserburg, G.J.

    1999-02-01T23:59:59.000Z

    This research program has moved ahead with success in several areas. The isotopic composition of osmium in seawater and in some rivers was directly determined for the first time. The concentration of osmium was first estimated in both seawater and rivers. A major effort was directed toward the transport of the U,Th series nuclides in a watershed in Sweden. A serious effort was directed at developing a transport model for the U,Th series nuclides in aquifers. A detailed study of {sup 238}U-{sup 230}Th dating of a cave in Israel was carried out collaboratively. The Os-Re fractionation between silicate and sulfide melts were determined in MORB basalts and glasses and the isotopic composition of Os was measured in sulfide samples.

  13. USABC Battery Separator Development

    Broader source: Energy.gov (indexed) [DOE]

    Derma Patches Gas Diffusion Food Packaging Specialty Medical Membranes Dialysis Plasma Separation Oxygenation O2 & CO2 Removal Food & Beverage Ink Processing Industrial Page...

  14. Three important parts of an integrated plant are reactors, separators and a heat exchanger network (HEN) for heat recovery. Within the process engineering community, much

    E-Print Network [OSTI]

    Skogestad, Sigurd

    exchanger network (HEN) for heat recovery. Within the process engineering community, much attention has beeni ABSTRACT Three important parts of an integrated plant are reactors, separators and a heat and in particular to optimal operation of HENs. The purpose of heat integration is to save energy, but the HEN also

  15. Ion Mobility Mass Spectrometry Direct Isotope Abundance Analysis

    SciTech Connect (OSTI)

    Manuel J. Manard, Stephan Weeks, Kevin Kyle

    2010-05-27T23:59:59.000Z

    The nuclear forensics community is currently engaged in the analysis of illicit nuclear or radioactive material for the purposes of non-proliferations and attribution. One technique commonly employed for gathering nuclear forensics information is isotope analysis. At present, the state-of-the-art methodology for obtaining isotopic distributions is thermal ionization mass spectrometry (TIMS). Although TIMS is highly accurate at determining isotope distributions, the technique requires an elementally pure sample to perform the measurement. The required radiochemical separations give rise to sample preparation times that can be in excess of one to two weeks. Clearly, the nuclear forensics community is in need of instrumentation and methods that can expedite their decision making process in the event of a radiological release or nuclear detonation. Accordingly, we are developing instrumentation that couples a high resolution IM drift cell to the front end of a MS. The IM cell provides a means of separating ions based upon their collision cross-section and mass-to-charge ratio (m/z). Two analytes with the same m/z, but with different collision cross-sections (shapes) would exit the cell at different times, essentially enabling the cell to function in a similar manner to a gas chromatography (GC) column. Thus, molecular and atomic isobaric interferences can be effectively removed from the ion beam. The mobility selected chemical species could then be introduced to a MS for high-resolution mass analysis to generate isotopic distributions of the target analytes. The outcome would be an IM/MS system capable of accurately measuring isotopic distributions while concurrently eliminating isobaric interferences and laboratory radiochemical sample preparation. The overall objective of this project is developing instrumentation and methods to produce near real-time isotope distributions with a modular mass spectrometric system that performs the required gas-phase chemistry and separations. The system couples a high-resolution ion mobility (IM) drift cell to the front end of a mass spectrometer (MS) allowing for chemical separation prior to isotope distribution analyses. This will yield isotope ratio measurement capabilities with minimal sample preparation.

  16. A FAST ASYMPTOTICALLY EFFICIENT ALGORITHM FOR BLIND SEPARATION OF A LINEAR MIXTURE OF BLOCK-WISE STATIONARY AUTOREGRESSIVE PROCESSES

    E-Print Network [OSTI]

    Yeredor, Arie

    diagonalization, blind source separation, autoregressiveprocesses, second-orderstatis- tics 1. INTRODUCTION Blind to This work was supported by Ministry of Education, Youth and Sports of the Czech Republic through the project

  17. A FAST ASYMPTOTICALLY EFFICIENT ALGORITHM FOR BLIND SEPARATION OF A LINEAR MIXTURE OF BLOCK-WISE STATIONARY AUTOREGRESSIVE PROCESSES

    E-Print Network [OSTI]

    Yeredor, Arie

    diagonalization, blind source separation, autoregressiveprocesses, second-orderstatis- tics 1. INTRODUCTION Blind by Ministry of Education, Youth and Sports of the Czech Republic through the project 1M0572 and by Grant

  18. Y-12 begins to separate lithium isotopes

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    now rapidly expanding nuclear weapons program. Unlike previous atomic weapons, these new thermonuclear weapons derived their explosive force from both fission and fusion of...

  19. Electromagnetic Isotope Separation Lab (EMIS) | ORNL

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645U.S. DOEThe Bonneville Power AdministrationField Campaign:INEAWater UseC Supports - Energy InnovationVehicles

  20. Stable Isotope Enrichment Capabilities at ORNL

    SciTech Connect (OSTI)

    Egle, Brian [ORNL; Aaron, W Scott [ORNL; Hart, Kevin J [ORNL

    2013-01-01T23:59:59.000Z

    The Oak Ridge National Laboratory (ORNL) and the US Department of Energy Nuclear Physics Program have built a high-resolution Electromagnetic Isotope Separator (EMIS) as a prototype for reestablishing a US based enrichment capability for stable isotopes. ORNL has over 60 years of experience providing enriched stable isotopes and related technical services to the international accelerator target community, as well as medical, research, industrial, national security, and other communities. ORNL is investigating the combined use of electromagnetic and gas centrifuge isotope separation technologies to provide research quantities (milligram to several kilograms) of enriched stable isotopes. In preparation for implementing a larger scale production facility, a 10 mA high-resolution EMIS prototype has been built and tested. Initial testing of the device has simultaneously collected greater than 98% enriched samples of all the molybdenum isotopes from natural abundance feedstock.

  1. VAPOR PRESSURE ISOTOPE EFFECTS IN THE MEASUREMENT OF ENVIRONMENTAL TRITIUM SAMPLES.

    SciTech Connect (OSTI)

    Kuhne, W.

    2012-12-03T23:59:59.000Z

    Standard procedures for the measurement of tritium in water samples often require distillation of an appropriate sample aliquot. This distillation process may result in a fractionation of tritiated water and regular light water due to the vapor pressure isotope effect, introducing either a bias or an additional contribution to the total tritium measurement uncertainty. The magnitude of the vapor pressure isotope effect is characterized as functions of the amount of water distilled from the sample aliquot and the heat settings for the distillation process. The tritium concentration in the distillate is higher than the tritium concentration in the sample early in the distillation process, it then sharply decreases due to the vapor pressure isotope effect and becomes lower than the tritium concentration in the sample, until the high tritium concentration retained in the boiling flask is evaporated at the end of the process. At that time, the tritium concentration in the distillate again overestimates the sample tritium concentration. The vapor pressure isotope effect is more pronounced the slower the evaporation and distillation process is conducted; a lower heat setting during the evaporation of the sample results in a larger bias in the tritium measurement. The experimental setup used and the fact that the current study allowed for an investigation of the relative change in vapor pressure isotope effect in the course of the distillation process distinguish it from and extend previously published measurements. The separation factor as a quantitative measure of the vapor pressure isotope effect is found to assume values of 1.034 {+-} 0.033, 1.052 {+-} 0.025, and 1.066 {+-} 0.037, depending on the vigor of the boiling process during distillation of the sample. A lower heat setting in the experimental setup, and therefore a less vigorous boiling process, results in a larger value for the separation factor. For a tritium measurement in water samples, this implies that the tritium concentration could be underestimated by 3 - 6%.

  2. Ultracapacitor separator

    DOE Patents [OSTI]

    Wei, Chang (Niskayuna, NY); Jerabek, Elihu Calvin (Glenmont, NY); LeBlanc, Jr., Oliver Harris (Schenectady, NY)

    2001-03-06T23:59:59.000Z

    An ultracapacitor includes two solid, nonporous current collectors, two porous electrodes separating the collectors, a porous separator between the electrodes and an electrolyte occupying the pores in the electrodes and separator. The electrolyte is a polar aprotic organic solvent and a salt. The porous separator comprises a wet laid cellulosic material.

  3. Online Catalog of Isotope Products from DOE's National Isotope Development Center

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    The National Isotope Development Center (NIDC) interfaces with the User Community and manages the coordination of isotope production across the facilities and business operations involved in the production, sale, and distribution of isotopes. A virtual center, the NIDC is funded by the Isotope Development and Production for Research and Applications (IDPRA) subprogram of the Office of Nuclear Physics in the U.S. Department of Energy Office of Science. The Isotope subprogram supports the production, and the development of production techniques of radioactive and stable isotopes that are in short supply for research and applications. Isotopes are high-priority commodities of strategic importance for the Nation and are essential for energy, medical, and national security applications and for basic research; a goal of the program is to make critical isotopes more readily available to meet domestic U.S. needs. This subprogram is steward of the Isotope Production Facility (IPF) at Los Alamos National Laboratory (LANL), the Brookhaven Linear Isotope Producer (BLIP) facility at BNL, and hot cell facilities for processing isotopes at ORNL, BNL and LANL. The subprogram also coordinates and supports isotope production at a suite of university, national laboratory, and commercial accelerator and reactor facilities throughout the Nation to promote a reliable supply of domestic isotopes. The National Isotope Development Center (NIDC) at ORNL coordinates isotope production across the many facilities and manages the business operations of the sale and distribution of isotopes.

  4. Particle separation

    DOE Patents [OSTI]

    Moosmuller, Hans (Reno, NV); Chakrabarty, Rajan K. (Reno, NV); Arnott, W. Patrick (Reno, NV)

    2011-04-26T23:59:59.000Z

    Embodiments of a method for selecting particles, such as based on their morphology, is disclosed. In a particular example, the particles are charged and acquire different amounts of charge, or have different charge distributions, based on their morphology. The particles are then sorted based on their flow properties. In a specific example, the particles are sorted using a differential mobility analyzer, which sorts particles, at least in part, based on their electrical mobility. Given a population of particles with similar electrical mobilities, the disclosed process can be used to sort particles based on the net charge carried by the particle, and thus, given the relationship between charge and morphology, separate the particles based on their morphology.

  5. from Isotope Production Facility

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Cancer-fighting treatment gets boost from Isotope Production Facility April 13, 2012 Isotope Production Facility produces cancer-fighting actinium 2:32 Isotope cancer treatment...

  6. Selective photoionisation of lutetium isotopes

    SciTech Connect (OSTI)

    D'yachkov, Aleksei B; Kovalevich, S K; Labozin, Valerii P; Mironov, Sergei M; Panchenko, Vladislav Ya; Firsov, Valerii A; Tsvetkov, G O; Shatalova, G G [National Research Centre 'Kurchatov Institute', Moscow (Russian Federation)

    2012-10-31T23:59:59.000Z

    A three-stage laser photoionisation scheme intended for enriching the {sup 176}Lu isotope from natural lutetium was considered. An investigation was made of the hyperfine structure of the second excited state 5d6s7s {yields} {sup 4}D{sub 3/2} with an energy of 37194 cm{sup -1} and the autoionisation state with an energy of 53375 cm{sup -1} of the {sup 176}Lu and {sup 175}Lu isotopes. The total electron momentum of the autoionisation level and the constant A of hyperfine magnetic interaction were determined. Due to a small value of the isotopic shift between {sup 176}Lu and {sup 175}Lu, appreciable selectivity of their separation may be achieved with individual hyperfine structure components. The first tentative enrichment of the 176Lu isotope was performed to a concentration of 60 % - 70 %. (laser applications and other topics in quantum electronics)

  7. Separation of Transmutation - and Fission-Produced Radioisotopes from Irradiated Beryllium

    SciTech Connect (OSTI)

    Troy J. Tranter; RIchard D. Tillotson; Nick R. Mann; Glen R. Longhurst

    2011-11-01T23:59:59.000Z

    The primary objective of this study was to test the effectiveness of a two-step solvent extraction-precipitation process for separating transmutation and fission products from irradiated beryllium. Beryllium metal was dissolved in nitric and fluoroboric acids. Isotopes of 241Am, 239Pu, 85Sr, 60Co, and 137Cs were then added to make a surrogate beryllium waste solution. A series of batch contacts was performed with the spiked simulant using chlorinated cobalt dicarbollide and polyethylene glycol diluted with sulfone to extract the isotopes of Cs and Sr. Another series of batch contacts was performed using a combination of octyl (phenyl)-N,Ndiisobutylcarbamoylmethylphosphine oxide in tributyl phosphate diluted with dodecane for extracting the isotopes of Pu and Am. The 60Co was separated by first forming a cobalt complex and then selectively precipitating the beryllium as a hydroxide. The results indicate that greater than 99.9% removal can be achieved for each radionuclide. Transuranic isotope contamination levels are reduced to less than 100 nCi/g, and sources of high beta-gamma radiation (60Co, 137Cs, and 90Sr) are reduced to levels that will allow the beryllium to be contact handled. The separation process may be applicable to a recycle or waste disposition scenario.

  8. Separation of toxic metal ions, hydrophilic hydrocarbons, hydrophobic fuel and halogenated hydrocarbons and recovery of ethanol from a process stream

    DOE Patents [OSTI]

    Kansa, Edward J. (Livermore, CA); Anderson, Brian L. (Lodi, CA); Wijesinghe, Ananda M. (Tracy, CA); Viani, Brian E. (Oakland, CA)

    1999-01-01T23:59:59.000Z

    This invention provides a process to tremendously reduce the bulk volume of contaminants obtained from an effluent stream produced subsurface remediation. The chemicals used for the subsurface remediation are reclaimed for recycling to the remediation process. Additional reductions in contaminant bulk volume are achieved by the ultra-violet light destruction of halogenated hydrocarbons, and the complete oxidation of hydrophobic fuel hydrocarbons and hydrophilic hydrocarbons. The contaminated bulk volume will arise primarily from the disposal of the toxic metal ions. The entire process is modular, so if there are any technological breakthroughs in one or more of the component process modules, such modules can be readily replaced.

  9. Separation of toxic metal ions, hydrophilic hydrocarbons, hydrophobic fuel and halogenated hydrocarbons and recovery of ethanol from a process stream

    DOE Patents [OSTI]

    Kansa, E.J.; Anderson, B.L.; Wijesinghe, A.M.; Viani, B.E.

    1999-05-25T23:59:59.000Z

    This invention provides a process to tremendously reduce the bulk volume of contaminants obtained from an effluent stream produced subsurface remediation. The chemicals used for the subsurface remediation are reclaimed for recycling to the remediation process. Additional reductions in contaminant bulk volume are achieved by the ultra-violet light destruction of halogenated hydrocarbons, and the complete oxidation of hydrophobic fuel hydrocarbons and hydrophilic hydrocarbons. The contaminated bulk volume will arise primarily from the disposal of the toxic metal ions. The entire process is modular, so if there are any technological breakthroughs in one or more of the component process modules, such modules can be readily replaced. 3 figs.

  10. Use of a submersible viscometer in the primary separation step of the hot water process for recovery of bitumen from tar sand

    SciTech Connect (OSTI)

    Schramm, L.L.

    1987-01-20T23:59:59.000Z

    The patent describes the primary separation step of the hot water process for extracting bitumen from tar sand in primary separation vessel. The bitumen floats upwardly in a tar sand slurry to form a froth layer, the coarse solids drop to form a tailings layer, and a middlings layer is formed between the froth and the tailings. The improvement described here comprises: providing a submerged viscometer in the middlings layer and actuating the viscometer to measure the viscosity of the middlings at one or more levels in the vertical column of middlings and produce signals, external of the vessel, which are indicative of the measurements; taking sufficient measurements to determine the viscosity of the region of maximum viscosity within the middlings layer and adjusting the viscosity of the middlings in response to the signals to maintain the maximum viscosity in the column below a predetermined value, whereby the flotation of the bitumen through the middlings layer to the froth layer is substantially enhanced.

  11. The influence of kinetics on the oxygen isotope composition of calcium carbonate

    E-Print Network [OSTI]

    Watkins, Jim

    The influence of kinetics on the oxygen isotope composition of calcium carbonate James M. Watkins a and calcium carbonate. Although oxygen isotope separation is expected on theoretical grounds, the temperature on equilibrium fractionation of oxygen isotopes between calcium carbonate and water. Equili- brium oxygen isotope

  12. Half-lives and branchings for {\\beta}-delayed neutron emission for neutron-rich Co-Cu isotopes in the r-process

    E-Print Network [OSTI]

    Hosmer, P; Aprahamian, A; Arndt, O; Clement, R R C; Estrade, A; Farouqi, K; Kratz, K -L; Liddick, S N; Lisetskiy, A F; Mantica, P F; Möller, P; Mueller, W F; Montes, F; Morton, A C; Ouellette, M; Pellegrini, E; Pereira, J; Pfeiffer, B; Reeder, P; Santi, P; Steiner, M; Stolz, A; Tomlin, B E; Walters, W B; Wöhr, A; 10.1103/PhysRevC.82.025806

    2010-01-01T23:59:59.000Z

    The {\\beta} decays of very neutron-rich nuclides in the Co-Zn region were studied experimentally at the National Superconducting Cyclotron Laboratory using the NSCL {\\beta}-counting station in conjunction with the neutron detector NERO. We measured the branchings for {\\beta}-delayed neutron emission (Pn values) for 74Co (18 +/- 15%) and 75-77Ni (10 +/- 2.8%, 14 +/- 3.6%, and 30 +/- 24%, respectively) for the first time, and remeasured the Pn values of 77-79Cu, 79,81Zn, and 82Ga. For 77-79Cu and for 81Zn we obtain significantly larger Pn values compared to previous work. While the new half-lives for the Ni isotopes from this experiment had been reported before, we present here in addition the first half-life measurements of 75Co (30 +/- 11 ms) and 80Cu (170+110 -50 ms). Our results are compared with theoretical predictions, and their impact on various types of models for the astrophysical rapid neutron-capture process (r-process) is explored. We find that with our new data, the classical r-process model is bet...

  13. SEPARATION OF HYDROGEN AND CARBON DIOXIDE USING A NOVEL MEMBRANE REACTOR IN ADVANCED FOSSIL ENERGY CONVERSION PROCESS

    SciTech Connect (OSTI)

    Shamsuddin Ilias

    2005-02-03T23:59:59.000Z

    Inorganic membrane reactors offer the possibility of combining reaction and separation in a single operation at high temperatures to overcome the equilibrium limitations experienced in conventional reactor configurations. Such attractive features can be advantageously utilized in a number of potential commercial opportunities, which include dehydrogenation, hydrogenation, oxidative dehydrogenation, oxidation and catalytic decomposition reactions. However, to be cost effective, significant technological advances and improvements will be required to solve several key issues which include: (a) permselective thin solid film, (b) thermal, chemical and mechanical stability of the film at high temperatures, and (c) reactor engineering and module development in relation to the development of effective seals at high temperature and high pressure. In this project, we are working on the development and application of palladium and palladium-silver alloy thin-film composite membranes in membrane reactor-separator configuration for simultaneous production and separation of hydrogen and carbon dioxide at high temperature. From our research on Pd-composite membrane, we have demonstrated that the new membrane has significantly higher hydrogen flux with very high perm-selectivity than any of the membranes commercially available. The steam reforming of methane by equilibrium shift in Pd-composite membrane reactor is being studied to demonstrate the potential application of this new development. A two-dimensional, pseudo-homogeneous membrane-reactor model was developed to investigate the steam-methane reforming (SMR) reactions in a Pd-based membrane reactor. Radial diffusion was taken into consideration to account for the concentration gradient in the radial direction due to hydrogen permeation through the membrane. With appropriate reaction rate expressions, a set of partial differential equations was derived using the continuity equation for the reaction system. The equations were solved by finite difference method. The solution of the model equations is complicated by the coupled reactions. At the inlet, if there is no hydrogen, rate expressions become singular. To overcome this problem, the first element of the reactor was treated as a continuous stirred tank reactor (CSTR). Several alternative numerical schemes were implemented in the solution algorithm to get a converged, stable solution. The model was also capable of handling steam-methane reforming reactions under non-membrane condition and equilibrium reaction conversions. Some of the numerical results were presented in the previous report. To test the membrane reactor model, we fabricated Pd-stainless steel membranes in tubular configuration using electroless plating method coupled with osmotic pressure. Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDX) were used to characterize the fabricated Pd-film composite membranes. Gas-permeation tests were performed to measure the permeability of hydrogen, nitrogen and helium using pure gas. The membranes showed excellent perm-selectivity for hydrogen. This makes the Pd-composite membrane attractive for selective separation and recovery of H{sub 2} from mixed gases at elevated temperature.

  14. Using High Performance Computing to Examine the Processes of Neurogenesis Underlying Pattern Separation and Completion of Episodic Information.

    SciTech Connect (OSTI)

    Aimone, James Bradley; Bernard, Michael Lewis; Vineyard, Craig Michael; Verzi, Stephen Joseph

    2014-10-01T23:59:59.000Z

    Adult neurogenesis in the hippocampus region of the brain is a neurobiological process that is believed to contribute to the brain's advanced abilities in complex pattern recognition and cognition. Here, we describe how realistic scale simulations of the neurogenesis process can offer both a unique perspective on the biological relevance of this process and confer computational insights that are suggestive of novel machine learning techniques. First, supercomputer based scaling studies of the neurogenesis process demonstrate how a small fraction of adult-born neurons have a uniquely larger impact in biologically realistic scaled networks. Second, we describe a novel technical approach by which the information content of ensembles of neurons can be estimated. Finally, we illustrate several examples of broader algorithmic impact of neurogenesis, including both extending existing machine learning approaches and novel approaches for intelligent sensing.

  15. Lead isotope study of the late Archean Lac des Iles palladium deposit, Canada: enrichment of platinum

    E-Print Network [OSTI]

    ARTICLE Lead isotope study of the late Archean Lac des Iles palladium deposit, Canada: enrichment Lead isotopic compositions of mineral separates are presented from the mineralized zones (Roby Province of Canada. Plagioclase separates show Pb isotope ratios similar to those of the late Archean

  16. Isotopically controlled semiconductors

    E-Print Network [OSTI]

    Haller, Eugene E.

    2006-01-01T23:59:59.000Z

    16 Isotopically Controlled Semiconductors Eugene E. Hallerof isotopically engineered semiconductors; for outstandingisotopically controlled semiconductor crystals. This article

  17. Recovering Americium and Curium from Mark-42 Target Materials- New Processing Approaches to Enhance Separations and Integrate Waste Stream Disposition - 12228

    SciTech Connect (OSTI)

    Patton, Brad D.; Benker, Dennis; Collins, Emory D.; Mattus, Catherine H.; Robinson, Sharon M.; Wham, Robert M. [Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States)

    2012-07-01T23:59:59.000Z

    Oak Ridge National Laboratory (ORNL) is investigating flowsheets to enhance processing efficiencies and to address waste streams associated with recovery of americium (Am) and curium (Cm) from Mark-42 (Mk-42) target materials stored at ORNL. The objective of this work was to identify the most effective flowsheet with which to process the 104 Mk-42 oxide capsules holding a total of 80 g of plutonium (Pu), 190 g of Cm, 480 g of Am, and 5 kg of lanthanide (Ln) oxides for the recovery and purification of the Am/Cm for future use as feedstock for heavy actinide production. Studies were also conducted to solidify the process flowsheet waste streams for disposal. ORNL is investigating flowsheets to enhance processing efficiencies and address waste streams associated with recovery of Am and Cm from Mk-42 target materials stored at ORNL. A series of small-scale runs are being performed to demonstrate an improved process to recover Am/Cm and to optimize the separations of Ln fission products from the Am/Cm constituents. The first of these runs has been completed using one of the Am/Cm/Ln oxide capsules stored at ORNL. The demonstration run showed promising results with a Ln DF of 40 for the Am/Cm product and an Am/Cm DF of 75 for the Ln product. In addition, the total losses of Am, Cm, and Ln to the waste solvents and raffinates were very low at <0.2%, 0.02%, and 0.04%, respectively. However, the Ln-actinide separation was less than desired. For future Reverse TALSPEAK demonstration runs, several parameters will be adjusted (flow rates, the ratio of scrub to strip stages, etc.) to improve the removal of Ln from the actinides. The next step will also include scale-up of the processing flowsheet to use more concentrated solutions (15 g/L Ln versus 5 g/L) and larger volumes and to recycle the HDEHP solvent. This should improve the overall processing efficiency and further reduce losses to waste streams. Studies have been performed with simulated wastes to develop solidification processes for disposal of the secondary waste streams generated by this flowsheet. Formulations were successfully developed for all the waste simulants. Additional tests with actual waste will be the next step in this effort. Future plans are to process all of the remaining 103 capsules in storage at ORNL. A nine-capsule test is now under way to provide additional information to scale-up the process to a target 20-capsule batch size for future processing runs. (authors)

  18. STATUS OF THE DEVELOPMENT OF IN-TANK/AT-TANK SEPARATIONS TECHNOLOGIES FOR FOR HIGH-LEVEL WASTE PROCESSING FOR THE U.S. DEPARTMENT OF ENERGY

    SciTech Connect (OSTI)

    Aaron, G.; Wilmarth, B.

    2011-09-19T23:59:59.000Z

    Within the U.S. Department of Energy's (DOE) Office of Technology Innovation and Development, the Office of Waste Processing manages a research and development program related to the treatment and disposition of radioactive waste. At the Savannah River (South Carolina) and Hanford (Washington) Sites, approximately 90 million gallons of waste are distributed among 226 storage tanks (grouped or collocated in 'tank farms'). This waste may be considered to contain mixed and stratified high activity and low activity constituent waste liquids, salts and sludges that are collectively managed as high level waste (HLW). A large majority of these wastes and associated facilities are unique to the DOE, meaning many of the programs to treat these materials are 'first-of-a-kind' and unprecedented in scope and complexity. As a result, the technologies required to disposition these wastes must be developed from basic principles, or require significant re-engineering to adapt to DOE's specific applications. Of particular interest recently, the development of In-tank or At-Tank separation processes have the potential to treat waste with high returns on financial investment. The primary objective associated with In-Tank or At-Tank separation processes is to accelerate waste processing. Insertion of the technologies will (1) maximize available tank space to efficiently support permanent waste disposition including vitrification; (2) treat problematic waste prior to transfer to the primary processing facilities at either site (i.e., Hanford's Waste Treatment and Immobilization Plant (WTP) or Savannah River's Salt Waste Processing Facility (SWPF)); and (3) create a parallel treatment process to shorten the overall treatment duration. This paper will review the status of several of the R&D projects being developed by the U.S. DOE including insertion of the ion exchange (IX) technologies, such as Small Column Ion Exchange (SCIX) at Savannah River. This has the potential to align the salt and sludge processing life cycle, thereby reducing the Defense Waste Processing Facility (DWPF) mission by 7 years. Additionally at the Hanford site, problematic waste streams, such as high boehmite and phosphate wastes, could be treated prior to receipt by WTP and thus dramatically improve the capacity of the facility to process HLW. Treatment of boehmite by continuous sludge leaching (CSL) before receipt by WTP will dramatically reduce the process cycle time for the WTP pretreatment facility, while treatment of phosphate will significantly reduce the number of HLW borosilicate glass canisters produced at the WTP. These and other promising technologies will be discussed.

  19. Apparatus for the separation of hydrophobic and hydrophilic particles using microbubble column flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, R.H.; Adel, G.T.; Luttrell, G.H.

    1995-03-14T23:59:59.000Z

    An apparatus is disclosed for the microbubble flotation separation of very fine and coarse particles, especially coal, and minerals so as to produce high purity and high recovery efficiency. This is accomplished through the use of a flotation column, microbubbles, recycling of the flotation pulp, and countercurrent wash water to gently wash the froth. Also disclosed are unique processes and apparatus for generating microbubbles for flotation in a highly efficient and inexpensive manner using either a porous tube or in-line static generators. 14 figs.

  20. Apparatus for the separation of hydrophobic and hydrophilic particles using microbubble column flotation together with a process and apparatus for generation of microbubbles

    DOE Patents [OSTI]

    Yoon, Roe-Hoan (Blacksburg, VA); Adel, Gregory T. (Blacksburg, VA); Luttrell, Gerald H. (Blacksburg, VA)

    1995-01-01T23:59:59.000Z

    An apparatus is disclosed for the microbubble flotation separation of very fine and coarse particles, especially coal, and minerals so as to produce high purity and high recovery efficiency. This is accomplished through the use of a flotation column, microbubbles, recycling of the flotation pulp, and countercurrent wash water to gently wash the froth. Also disclosed are unique processes and apparatus for generating microbubbles for flotation in a highly efficient and inexpensive manner using either a porous tube or in-line static generators.

  1. Separation of Fischer-Tropsch Wax from Catalyst Using Near-Critical Fluid Extraction: Analysis of Process

    E-Print Network [OSTI]

    Kilpatrick, Peter K.

    the flowsheet contained only one product recovery unit. Self-sufficiency was obtained with multiple recovery for the recovery of heavy normal paraffins from a Fischer-Tropsch slurry reactor has been analyzed. Process extraction temperatures and higher slurry flowrates, but had several attractive features such as lower vapor

  2. Half-lives and branchings for {beta}-delayed neutron emission for neutron-rich Co-Cu isotopes in the r-process

    SciTech Connect (OSTI)

    Hosmer, P.; Estrade, A.; Montes, F.; Ouellette, M.; Pellegrini, E. [National Superconducting Cyclotron Laboratory, Michigan State University, East Lansing, Michigan 48824 (United States); Department of Physics and Astronomy, Michigan State University, East Lansing, Michigan 48824 (United States); Schatz, H. [National Superconducting Cyclotron Laboratory, Michigan State University, East Lansing, Michigan 48824 (United States); Department of Physics and Astronomy, Michigan State University, East Lansing, Michigan 48824 (United States); Joint Institute for Nuclear Astrophysics, Michigan State University, East Lansing, Michigan 48824 (United States); Aprahamian, A. [Department of Physics and Joint Institute for Nuclear Astrophysics, University of Notre Dame, Notre Dame, Indiana 46556 (United States); Arndt, O.; Pfeiffer, B. [Institut fuer Kernchemie, Universitaet Mainz, Fritz-Strassmann Weg 2, D-55128 Mainz (Germany); HGF Virtuelles Institut fuer Kernstruktur und Nukleare Astrophysik (Germany); Clement, R. R. C.; Mueller, W. F.; Morton, A. C.; Pereira, J.; Santi, P.; Steiner, M.; Stolz, A. [National Superconducting Cyclotron Laboratory, Michigan State University, East Lansing, Michigan 48824 (United States); Farouqi, K. [Department of Astronomy and Astrophysics and Joint Institute for Nuclear Astrophysics, University of Chicago, Chicago, IL 60637 (United States); Kratz, K.-L. [HGF Virtuelles Institut fuer Kernstruktur und Nukleare Astrophysik (Germany); Max-Planck-Institut fuer Chemie (Otto-Hahn-Institut), J.-J.-Becherweg 27, D-55128 Mainz (Germany); Liddick, S. N.; Mantica, P. F. [National Superconducting Cyclotron Laboratory, Michigan State University, East Lansing, Michigan 48824 (United States); Department of Chemistry, Michigan State University, East Lansing, Michigan 48824 (United States)

    2010-08-15T23:59:59.000Z

    The {beta} decays of very neutron-rich nuclides in the Co-Zn region were studied experimentally at the National Superconducting Cyclotron Laboratory using the NSCL {beta}-counting station in conjunction with the neutron detector NERO. We measured the branchings for {beta}-delayed neutron emission (P{sub n} values) for {sup 74}Co (18{+-}15%) and {sup 75-77}Ni (10{+-}2.8%, 14{+-}3.6%, and 30{+-}24%, respectively) for the first time, and remeasured the P{sub n} values of {sup 77-79}Cu, {sup 79,81}Zn, and {sup 82}Ga. For {sup 77-79}Cu and for {sup 81}Zn we obtain significantly larger P{sub n} values compared to previous work. While the new half-lives for the Ni isotopes from this experiment had been reported before, we present here in addition the first half-life measurements of {sup 75}Co (30{+-}11 ms) and {sup 80}Cu (170{sub -50}{sup +110} ms). Our results are compared with theoretical predictions, and their impact on various types of models for the astrophysical rapid neutron-capture process (r-process) is explored. We find that with our new data, the classical r-process model is better able to reproduce the A=78-80 abundance pattern inferred from the solar abundances. The new data also influence r-process models based on the neutrino-driven high-entropy winds in core collapse supernovae.

  3. Coal liquefaction process streams characterization and evaluation: Application of liquid chromatographic separation methods to THF-soluble portions of integrated two-stage coal liquefaction resids

    SciTech Connect (OSTI)

    Green, J.B.; Pearson, C.D.; Young, L.L.; Green, J.A. [National Inst. for Petroleum and Energy Research, Bartlesville, OK (United States)

    1992-05-01T23:59:59.000Z

    This study demonstrated the feasibility of using non-aqueous ion exchange liquid chromatography (NIELC) for the examination of the tetrahydrofuran (THF)-soluble distillation resids and THF-soluble whole oils derived from direct coal liquefaction. The technique can be used to separate the material into a number of acid, base, and neutral fractions. Each of the fractions obtained by NIELC was analyzed and then further fractionated by high-performance liquid chromatography (HPLC). The separation and analysis schemes are given in the accompanying report. With this approach, differences can be distinguished among samples obtained from different process streams in the liquefaction plant and among samples obtained at the same sampling location, but produced from different feed coals. HPLC was directly applied to one THF-soluble whole process oil without the NIELC preparation, with limited success. The direct HPLC technique used was directed toward the elution of the acid species into defined classes. The non-retained neutral and basic components of the oil were not analyzable by the direct HPLC method because of solubility limitations. Sample solubility is a major concern in the application of these techniques.

  4. Nuclear criticality safety bounding analysis for the in-tank-precipitation (ITP) process, impacted by fissile isotopic weight fractions

    SciTech Connect (OSTI)

    Bess, C.E.

    1994-04-22T23:59:59.000Z

    The In-Tank Precipitation process (ITP) receives High Level Waste (HLW) supernatant liquid containing radionuclides in waste processing tank 48H. Sodium tetraphenylborate, NaTPB, and monosodium titanate (MST), NaTi{sub 2}O{sub 5}H, are added for removal of radioactive Cs and Sr, respectively. In addition to removal of radio-strontium, MST will also remove plutonium and uranium. The majority of the feed solutions to ITP will come from the dissolution of supernate that had been concentrated by evaporation to a crystallized salt form, commonly referred to as saltcake. The concern for criticality safety arises from the adsorption of U and Pt onto MST. If sufficient mass and optimum conditions are achieved then criticality is credible. The concentration of u and Pt from solution into the smaller volume of precipitate represents a concern for criticality. This report supplements WSRC-TR-93-171, Nuclear Criticality Safety Bounding Analysis For The In-Tank-Precipitation (ITP) Process. Criticality safety in ITP can be analyzed by two bounding conditions: (1) the minimum safe ratio of MST to fissionable material and (2) the maximum fissionable material adsorption capacity of the MST. Calculations have provided the first bounding condition and experimental analysis has established the second. This report combines these conditions with canyon facility data to evaluate the potential for criticality in the ITP process due to the adsorption of the fissionable material from solution. In addition, this report analyzes the potential impact of increased U loading onto MST. Results of this analysis demonstrate a greater safety margin for ITP operations than the previous analysis. This report further demonstrates that the potential for criticality in the ITP process due to adsorption of fissionable material by MST is not credible.

  5. Quantifying Uranium Isotope Ratios Using Resonance Ionization Mass Spectrometry: The Influence of Laser Parameters on Relative Ionization Probability

    SciTech Connect (OSTI)

    Isselhardt, B H

    2011-09-06T23:59:59.000Z

    Resonance Ionization Mass Spectrometry (RIMS) has been developed as a method to measure relative uranium isotope abundances. In this approach, RIMS is used as an element-selective ionization process to provide a distinction between uranium atoms and potential isobars without the aid of chemical purification and separation. We explore the laser parameters critical to the ionization process and their effects on the measured isotope ratio. Specifically, the use of broad bandwidth lasers with automated feedback control of wavelength was applied to the measurement of {sup 235}U/{sup 238}U ratios to decrease laser-induced isotopic fractionation. By broadening the bandwidth of the first laser in a 3-color, 3-photon ionization process from a bandwidth of 1.8 GHz to about 10 GHz, the variation in sequential relative isotope abundance measurements decreased from >10% to less than 0.5%. This procedure was demonstrated for the direct interrogation of uranium oxide targets with essentially no sample preparation. A rate equation model for predicting the relative ionization probability has been developed to study the effect of variation in laser parameters on the measured isotope ratio. This work demonstrates that RIMS can be used for the robust measurement of uranium isotope ratios.

  6. Development of Highly Durable and Reactive Regenerable Magnesium-Based Sorbents for CO2 Separation in Coal Gasification Process

    SciTech Connect (OSTI)

    Javad Abbasian; Armin Hassanzadeh Khayyat; Rachid B. Slimane

    2005-06-01T23:59:59.000Z

    The specific objective of this project was to develop physically durable and chemically regenerable MgO-based sorbents that can remove carbon dioxide from raw coal gas at operating condition prevailing in IGCC processes. A total of sixty two (62) different sorbents were prepared in this project. The sorbents were prepared either by various sol-gel techniques (22 formulations) or modification of dolomite (40 formulations). The sorbents were prepared in the form of pellets and in granular forms. The solgel based sorbents had very high physical strength, relatively high surface area, and very low average pore diameter. The magnesium content of the sorbents was estimated to be 4-6 % w/w. To improve the reactivity of the sorbents toward CO{sub 2}, The sorbents were impregnated with potassium salts. The potassium content of the sorbents was about 5%. The dolomite-based sorbents were prepared by calcination of dolomite at various temperature and calcination environment (CO{sub 2} partial pressure and moisture). Potassium carbonate was added to the half-calcined dolomite through wet impregnation method. The estimated potassium content of the impregnated sorbents was in the range of 1-6% w/w. In general, the modified dolomite sorbents have significantly higher magnesium content, larger pore diameter and lower surface area, resulting in significantly higher reactivity compared to the sol-gel sorbents. The reactivities of a number of sorbents toward CO{sub 2} were determined in a Thermogravimetric Analyzer (TGA) unit. The results indicated that at the low CO{sub 2} partial pressures (i.e., 1 atm), the reactivities of the sorbents toward CO{sub 2} are very low. At elevated pressures (i.e., CO{sub 2} partial pressure of 10 bar) the maximum conversion of MgO obtained with the sol-gel based sorbents was about 5%, which corresponds to a maximum CO{sub 2} absorption capacity of less than 1%. The overall capacity of modified dolomite sorbents were at least one order of magnitude higher than those of the sol-gel based sorbents. The results of the tests conducted with various dolomite-based sorbent indicate that the reactivity of the modified dolomite sorbent increases with increasing potassium concentration, while higher calcination temperature adversely affects the sorbent reactivity. Furthermore, the results indicate that as long as the absorption temperature is well below the equilibrium temperature, the reactivity of the sorbent improves with increasing temperature (350-425 C). As the temperature approaches the equilibrium temperature, because of the significant increase in the rate of reverse (i.e., regeneration) reaction, the rate of CO{sub 2} absorption decreases. The results of cyclic tests show that the reactivity of the sorbent gradually decreases in the cyclic process. To improve long-term durability (i.e., reactivity and capacity) of the sorbent, the sorbent was periodically re-impregnated with potassium additive and calcined. The results indicate that, in general, re-treatment improves the performance of the sorbent, and that, the extent of improvement gradually decreases in the cyclic process. The presence of steam significantly enhances the sorbent reactivity and significantly decreases the rate of decline in sorbent deactivation in the cyclic process.

  7. Sulfur Isotopes as Indicators of Amended Bacterial Sulfate Reduction...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    of Amended Bacterial Sulfate Reduction Processes Influencing Field Scale Uranium Bioremediation. Sulfur Isotopes as Indicators of Amended Bacterial Sulfate Reduction Processes...

  8. Substituted polyacetylene separation membrane

    DOE Patents [OSTI]

    Pinnau, Ingo (Palo Alto, CA); Morisato, Atsushi (Tokyo, JP)

    1998-01-13T23:59:59.000Z

    A separation membrane useful for gas separation, particularly separation of C.sub.2+ hydrocarbons from natural gas. The invention encompasses the membrane itself, methods of making it and processes for using it. The membrane comprises a polymer having repeating units of a hydrocarbon-based, disubstituted polyacetylene, having the general formula: ##STR1## wherein R.sub.1 is chosen from the group consisting of C.sub.1 -C.sub.4 alkyl and phenyl, and wherein R.sub.2 is chosen from the group consisting of hydrogen and phenyl. In the most preferred embodiment, the membrane comprises poly(4-methyl-2-pentyne) ›PMP!. The membrane exhibits good chemical resistance and has super-glassy properties with regard to separating certain large, condensable permeant species from smaller, less-condensable permeant species. The membranes may also be useful in other fluid separations.

  9. Substituted polyacetylene separation membrane

    DOE Patents [OSTI]

    Pinnau, I.; Morisato, Atsushi

    1998-01-13T23:59:59.000Z

    A separation membrane is described which is useful for gas separation, particularly separation of C{sub 2+} hydrocarbons from natural gas. The invention encompasses the membrane itself, methods of making it and processes for using it. The membrane comprises a polymer having repeating units of a hydrocarbon-based, disubstituted polyacetylene, having the general formula shown in the accompanying diagram, wherein R{sub 1} is chosen from the group consisting of C{sub 1}-C{sub 4} alkyl and phenyl, and wherein R{sub 2} is chosen from the group consisting of hydrogen and phenyl. In the most preferred embodiment, the membrane comprises poly(4-methyl-2-pentyne) [PMP]. The membrane exhibits good chemical resistance and has super-glassy properties with regard to separating certain large, condensable permeant species from smaller, less-condensable permeant species. The membranes may also be useful in other fluid separations. 4 figs.

  10. Innovative Separations Technologies

    SciTech Connect (OSTI)

    J. Tripp; N. Soelberg; R. Wigeland

    2011-05-01T23:59:59.000Z

    Reprocessing used nuclear fuel (UNF) is a multi-faceted problem involving chemistry, material properties, and engineering. Technology options are available to meet a variety of processing goals. A decision about which reprocessing method is best depends significantly on the process attributes considered to be a priority. New methods of reprocessing that could provide advantages over the aqueous Plutonium Uranium Reduction Extraction (PUREX) and Uranium Extraction + (UREX+) processes, electrochemical, and other approaches are under investigation in the Fuel Cycle Research and Development (FCR&D) Separations Campaign. In an attempt to develop a revolutionary approach to UNF recycle that may have more favorable characteristics than existing technologies, five innovative separations projects have been initiated. These include: (1) Nitrogen Trifluoride for UNF Processing; (2) Reactive Fluoride Gas (SF6) for UNF Processing; (3) Dry Head-end Nitration Processing; (4) Chlorination Processing of UNF; and (5) Enhanced Oxidation/Chlorination Processing of UNF. This report provides a description of the proposed processes, explores how they fit into the Modified Open Cycle (MOC) and Full Recycle (FR) fuel cycles, and identifies performance differences when compared to 'reference' advanced aqueous and fluoride volatility separations cases. To be able to highlight the key changes to the reference case, general background on advanced aqueous solvent extraction, advanced oxidative processes (e.g., volumetric oxidation, or 'voloxidation,' which is high temperature reaction of oxide UNF with oxygen, or modified using other oxidizing and reducing gases), and fluorination and chlorination processes is provided.

  11. OREGON STATE UNIVERSITY (OSU) TRAINING RESEARCH ISOTOPE GENERAL ATOMICS (TRIGA) OVERPACK CLOSURE WELDING PROCESS PARAMETER DEVELOPMENT & QUALIFICATION

    SciTech Connect (OSTI)

    CANNELL, G.R.

    2006-09-11T23:59:59.000Z

    Spent Nuclear Fuel (SNF) from the Oregon State University (OSU) TRIGA{reg_sign} Reactor is currently being stored in thirteen 55-gallon drums at the Hanford Site's low-level burial grounds. This fuel is soon to be retrieved from buried storage and packaged into new containers (overpacks) for interim storage at the Hanford Interim Storage Area (ISA). One of the key activities associated with this effort is final closure of the overpack by welding. The OSU fuel is placed into an overpack, a head inserted into the overpack top, and welded closed. Weld quality, for typical welded fabrication, is established through post-weld testing and nondestructive examination (NDE); however, in this case, once the SNF is placed into the overpack, routine testing and NDE are not feasible. An alternate approach is to develop and qualify the welding process/parameters, demonstrate beforehand that they produce the desired weld quality, and then verify parameter compliance during production welding. Fluor engineers have developed a Gas Tungsten Arc Welding (GTAW) technique and parameters, demonstrating that weld quality requirements for closure of packaged SNF overpacks are met, using this alternate approach. The following reviews the activities performed for this development and qualification effort.

  12. Organic Separation Test Results

    SciTech Connect (OSTI)

    Russell, Renee L.; Rinehart, Donald E.; Peterson, Reid A.

    2014-09-22T23:59:59.000Z

    Separable organics have been defined as “those organic compounds of very limited solubility in the bulk waste and that can form a separate liquid phase or layer” (Smalley and Nguyen 2013), and result from three main solvent extraction processes: U Plant Uranium Recovery Process, B Plant Waste Fractionation Process, and Plutonium Uranium Extraction (PUREX) Process. The primary organic solvents associated with tank solids are TBP, D2EHPA, and NPH. There is concern that, while this organic material is bound to the sludge particles as it is stored in the tanks, waste feed delivery activities, specifically transfer pump and mixer pump operations, could cause the organics to form a separated layer in the tank farms feed tank. Therefore, Washington River Protection Solutions (WRPS) is experimentally evaluating the potential of organic solvents separating from the tank solids (sludge) during waste feed delivery activities, specifically the waste mixing and transfer processes. Given the Hanford Tank Waste Treatment and Immobilization Plant (WTP) waste acceptance criteria per the Waste Feed Acceptance Criteria document (24590-WTP-RPT-MGT-11-014) that there is to be “no visible layer” of separable organics in the waste feed, this would result in the batch being unacceptable to transfer to WTP. This study is of particular importance to WRPS because of these WTP requirements.

  13. Analysis of hydrogen isotope mixtures

    DOE Patents [OSTI]

    Villa-Aleman, Eliel (Aiken, SC)

    1994-01-01T23:59:59.000Z

    An apparatus and method for determining the concentrations of hydrogen isotopes in a sample. Hydrogen in the sample is separated from other elements using a filter selectively permeable to hydrogen. Then the hydrogen is condensed onto a cold finger or cryopump. The cold finger is rotated as pulsed laser energy vaporizes a portion of the condensed hydrogen, forming a packet of molecular hydrogen. The desorbed hydrogen is ionized and admitted into a mass spectrometer for analysis.

  14. Geohydrologic feasibility study of the Piceance Basin of Colorado for the potential applicability of Jack W. McIntyre`s patented gas/produced water separation process

    SciTech Connect (OSTI)

    Kieffer, F.

    1994-02-01T23:59:59.000Z

    Geraghty & Miller, Inc. of Midland, Texas conducted geologic and hydrologic feasibility studies of the potential applicability of Jack McIntyre`s patented process for the recovery of natural gas from coalbed/sand formations in the Piceance Basin through literature surveys. Jack McIntyre`s tool separates produced water from gas and disposes of the water downhole into aquifers unused because of poor water quality, uneconomic lifting costs or poor aquifer deliverability. The beneficial aspects of this technology are two fold. The process increases the potential for recovering previously uneconomic gas resources by reducing produced water lifting, treatment and disposal costs. Of greater importance is the advantage of lessening the environmental impact of produced water by downhole disposal. Results from the survey indicate that research in the Piceance Basin includes studies of the geologic, hydrogeologic, conventional and unconventional recovery oil and gas technologies. Available information is mostly found centered upon the geology and hydrology for the Paleozoic and Mesozoic sediments. Lesser information is available on production technology because of the limited number of wells currently producing in the basin. Limited information is available on the baseline geochemistry of the coal/sand formation waters and that of the potential disposal zones. No determination was made of the compatibility of these waters. The study also indicates that water is often produced in variable quantities with gas from several gas productive formations which would indicate that there are potential applications for Jack McIntyre`s patented tool in the Piceance Basin.

  15. Study of the Role of Terrestrial Processes in the Carbon Cycle Based on Measurements of the Abundance and Isotopic Composition of Atmospheric CO2

    SciTech Connect (OSTI)

    Stephen C. Piper; Ralph F. Keeling

    2012-01-03T23:59:59.000Z

    The main objective of this project was to continue research to develop carbon cycle relationships related to the land biosphere based on remote measurements of atmospheric CO2 concentration and its isotopic ratios 13C/12C, 18O/16O, and 14C/12C. The project continued time-series observations of atmospheric carbon dioxide and isotopic composition begun by Charles D. Keeling at remote sites, including Mauna Loa, the South Pole, and eight other sites. Using models of varying complexity, the concentration and isotopic measurements were used to study long-term change in the interhemispheric gradients in CO2 and 13C/12C to assess the magnitude and evolution of the northern terrestrial carbon sink, to study the increase in amplitude of the seasonal cycle of CO2, to use isotopic data to refine constraints on large scale changes in isotopic fractionation which may be related to changes in stomatal conductance, and to motivate improvements in terrestrial carbon cycle models. The original proposal called for a continuation of the new time series of 14C measurements but subsequent descoping to meet budgetary constraints required termination of measurements in 2007.

  16. Process for separating, especially in multiple stages, acid components such as CO/sub 2/, HCN and specifically H/sub 2/S, from gases, especially from coke oven gases, by means of ammonia recirculation scrubbing

    SciTech Connect (OSTI)

    Bauer, H.K.; Otte, E.A.W.

    1984-10-16T23:59:59.000Z

    A process of separating in multiple stages acid components in coke oven gas such as CO/sub 2/, HCN and particularly H/sub 2/S by ammonia scrubbing wherein the ammonia used in scrubbing is deacidified to remove the acid components and is recirculated to the scrubbing process at least in part as substantially pure liquid ammonia.

  17. Isotopes Tell Origin and Operation of the Sun

    E-Print Network [OSTI]

    O. Manuel; Sumeet A. Kamat; Michael Mozina

    2005-09-28T23:59:59.000Z

    The Iron Sun formed on the collapsed core of a supernova and now acts as a magnetic plasma diffuser, as did the precursor star, separating ions by mass. This process covers the solar surface with lightweight elements and with lighter isotopes of each element. Running difference images expose rigid, iron-rich structures below the fluid photosphere made of lightweight elements. The energy source for the Sun and ordinary stars seems to be neutron-emission and neutron-decay, with partial fusion of the decay product, rather than simple fusion of hydrogen into helium or heavier elements. Neutron-emission from the solar core and neutron-decay generate about sixty five percent of solar luminosity and H-fusion generates about thirty-five percent. The upward flow of H ions maintains mass-separation in the Sun. Only about one percent of this neutron decay product survives its upward journey to depart as solar-wind hydrogen.

  18. Fluorine separation and generation device

    DOE Patents [OSTI]

    The Regents of the University of California (Oakland, CA)

    2008-12-23T23:59:59.000Z

    A process and apparatus for the electrolytic separation of fluorine from a mixture of gases is disclosed. Also described is the process and apparatus for the generation of fluorine from fluorine/fluoride containing solids, liquids or gases.

  19. Fluorine separation and generation device

    DOE Patents [OSTI]

    Jacobson, Craig P. (Moraga, CA); Visco, Steven J. (Berkeley, CA); DeJonghe, Lutgard C. (Lafayette, CA); Stefan, Constantin I. (Hayward, CA)

    2010-03-02T23:59:59.000Z

    A process and apparatus for the electrolytic separation of fluorine from a mixture of gases is disclosed. Also described is the process and apparatus for the generation of fluorine from fluorine/fluoride containing solids, liquids or gases.

  20. Isotope Science

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    cGMP compliant processing. * Plutonium facilities for Am-241 processing. * Chemical metallurgy facilities and additional hot cells. LANSCE national user facilities, including the...

  1. The production of fuels and chemicals from food processing wastes using a novel fermenter separator. Annual progress report, January 1991--December 1991

    SciTech Connect (OSTI)

    Dale, M.C.; Venkatesh, K.V.; Choi, Hojoon; Moelhman, M.; Saliceti, L.; Okos, M.R.; Wankat, P.C.

    1991-12-01T23:59:59.000Z

    During 1991, considerable progress was made on the waste utilization project. Two small Wisconsin companies have expressed an interest in promoting and developing the ICRS technology. Pilot plant sites at (1) Hopkinton, IA, for a sweet whey plant, and Beaver Dam WI, for an acid whey site have been under development siting ICRS operations. The Hopkinton, IA site is owned and operated by Permeate Refining Inc., who have built a batch ethanol plant across the street from Swiss Valley Farms cheddar cheese operations. Permeate from Swiss Valley is piped across to PRI. PRI has signed a contract to site a 300--500,000 gallon/yr to ICRS pilot plant. They feel that the lower labor, lower energy, continuous process offered by the ICRS will substantially improve their profitability. Catalytics, Inc, is involved with converting whey from a Kraft cream cheese operation to ethanol and yeast. A complete project including whey concentration, sterilization, and yeast growth has been designed for this site. Process design improvements with the ICRS focussed on ethanol recovery techniques during this year`s project. A solvent absorption/extractive distillation (SAED) process has been developed which offers the capability of obtaining an anhydrous ethanol product from vapors off 3 to 9% ethanol solutions using very little energy for distillation. Work on products from waste streams was also performed. a. Diacetyl as a high value flavor compound was very successfully produced in a Stirred Tank Reactor w/Separation. b. Yeast production from secondary carbohydrates in the whey, lactic acid, and glycerol was studied. c. Lactic acid production from cellulose and lactose studies continued. d. Production of anti-fungal reagents by immobilized plant cells; Gossypol has antifungal properties and is produced by G. arboretum.

  2. RAPID FUSION METHOD FOR DETERMINATION OF PLUTONIUM ISOTOPES IN LARGE RICE SAMPLES

    SciTech Connect (OSTI)

    Maxwell, S.

    2013-03-01T23:59:59.000Z

    A new rapid fusion method for the determination of plutonium in large rice samples has been developed at the Savannah River National Laboratory (Aiken, SC, USA) that can be used to determine very low levels of plutonium isotopes in rice. The recent accident at Fukushima Nuclear Power Plant in March, 2011 reinforces the need to have rapid, reliable radiochemical analyses for radionuclides in environmental and food samples. Public concern regarding foods, particularly foods such as rice in Japan, highlights the need for analytical techniques that will allow very large sample aliquots of rice to be used for analysis so that very low levels of plutonium isotopes may be detected. The new method to determine plutonium isotopes in large rice samples utilizes a furnace ashing step, a rapid sodium hydroxide fusion method, a lanthanum fluoride matrix removal step, and a column separation process with TEVA Resin? cartridges. The method can be applied to rice sample aliquots as large as 5 kg. Plutonium isotopes can be determined using alpha spectrometry or inductively-coupled plasma mass spectrometry (ICP-MS). The method showed high chemical recoveries and effective removal of interferences. The rapid fusion technique is a rugged sample digestion method that ensures that any refractory plutonium particles are effectively digested. The MDA for a 5 kg rice sample using alpha spectrometry is 7E-5 mBq g{sup -1}. The method can easily be adapted for use by ICP-MS to allow detection of plutonium isotopic ratios.

  3. Stable isotope studies

    SciTech Connect (OSTI)

    Ishida, T.

    1992-01-01T23:59:59.000Z

    The research has been in four general areas: (1) correlation of isotope effects with molecular forces and molecular structures, (2) correlation of zero-point energy and its isotope effects with molecular structure and molecular forces, (3) vapor pressure isotope effects, and (4) fractionation of stable isotopes. 73 refs, 38 figs, 29 tabs.

  4. Pressure Swing Absorption Device and Process for Separating CO{sub 2} from Shifted Syngas and its Capture for Subsequent Storage

    SciTech Connect (OSTI)

    Sirkar, Kamalesh; Jie, Xingming; Chau, John; Obuskovic, Gordana

    2013-03-31T23:59:59.000Z

    Using the ionic liquid (IL) 1-butyl-3-methylimidazolium dicyanamide ([bmim][DCA]) as the absorbent on the shell side of a membrane module containing either a porous hydrophobized ceramic tubule or porous hydrophobized polyether ether ketone (PEEK) hollow fiber membranes, studies for CO{sub 2} removal from hot simulated pre-combustion shifted syngas were carried out by a novel pressure swing membrane absorption (PSMAB) process. Helium was used as a surrogate for H{sub 2} in a simulated shifted syngas with CO{sub 2} around 40% (dry gas basis). In this cyclic separation process, the membrane module was used to achieve non-dispersive gas absorption from a high-pressure feed gas (689-1724 kPag; 100-250 psig) at temperatures between 25-1000C into a stationary absorbent liquid on the module shell side during a certain part of the cycle followed by among other cycle steps controlled desorption of the absorbed gases from the liquid in the rest of the cycle. Two product streams were obtained, one He-rich and the other CO{sub 2}-rich. Addition of polyamidoamine (PAMAM) dendrimer of generation 0 to IL [bmim][DCA] improved the system performance at higher temperatures. The solubilities of CO{sub 2} and He were determined in the ionic liquid with or without the dendrimer in solution as well as in the presence or absence of moisture; polyethylene glycol (PEG) 400 was also studied as a replacement for the IL. The solubility selectivity of the ionic liquid containing the dendrimer for CO{sub 2} over helium was considerably larger than that for the pure ionic liquid. The solubility of CO{sub 2} and CO{sub 2}-He solubility selectivity of PEG 400 and a solution of the dendrimer in PEG 400 were higher than the corresponding ones in the IL, [bmim][DCA]. A mathematical model was developed to describe the PSMAB process; a numerical solution of the governing equations described successfully the observed performance of the PSMAB process for the pure ionic liquid-based system.

  5. {sup 238}U-{sup 234}U-{sup 230}Th chronometry of Fe-Mn crusts: Growth processes and recovery of thorium isotopic ratios of seawater

    SciTech Connect (OSTI)

    Chabaux, F.; Cohen, A.S.; O`Nions, R.K. [Univ. of Cambridge (United Kingdom)] [Univ. of Cambridge (United Kingdom); Hein, J.R. [Geological Survey, Menlo Park, CA (United States)] [Geological Survey, Menlo Park, CA (United States)

    1995-02-01T23:59:59.000Z

    Comparison of ({sup 234}U){sub excess}/({sup 238}U) and ({sup 230}Th)/({sup 232}Th) activity ratios in oceanic Fe-Mn deposits provides a method for assessing the closed-system behaviour of {sup 238}U-{sup 234}U-{sup 230}Th, as well as variations in the initial uranium and thorium isotopic ratios of the precipitated metal oxides. This approach is illustrated using a Fe-Mn crust from Lotab seamount (Marshall Islands, west equatorial Pacific). Here we report uranium and thorium isotopic compositions in five subsamples from the surface of one large 5 cm diameter botyroid of this crust, and from two depth profiles of the outermost rim of the same botyroid. The decrease of ({sup 234}U){sub excess}/({sup 238}U) and ({sup 230}Th/{sup 232}Th) activity ratio with depth in the two profiles gives mean growth rates, for the last 150 ka, of 7.8 {+-} 2 mm/Ma and 6.6 {+-} 1 mm/Ma, respectively. All data points (surface and core samples) but one, define a linear correlation in the Ln ({sup 230}Th/{sup 232}Th) - Ln [({sup 234}U){sub excess}({sup 238}U)] diagram. This correlation indicates that for all points the U-Th system remained closed after the Fe-Mn layer precipitated, and that the different samples possessed the same initial Uranium and thorium isotope ratios. Furthermore, these results show that the preserved surface of this Fe-Mn crust may not be the present-day growth surface, and that the thorium and uranium isotopic ratios of seawater in west equatorial Pacific have not changed during the past 150 ka. The initial thorium activity ratio is estimated from the correlation obtained between Ln({sup 230}Th/{sup 232}Th) and Ln [({sup 234}U){sub excess}/({sup 238}U)].

  6. Gas separation membrane module assembly

    DOE Patents [OSTI]

    Wynn, Nicholas P (Palo Alto, CA); Fulton, Donald A. (Fairfield, CA)

    2009-03-31T23:59:59.000Z

    A gas-separation membrane module assembly and a gas-separation process using the assembly. The assembly includes a set of tubes, each containing gas-separation membranes, arranged within a housing. The housing contains a tube sheet that divides the space within the housing into two gas-tight spaces. A permeate collection system within the housing gathers permeate gas from the tubes for discharge from the housing.

  7. Membrane separation of hydrocarbons

    DOE Patents [OSTI]

    Chang, Y. Alice (Des Plaines, IL); Kulkarni, Sudhir S. (Hoffman Estates, IL); Funk, Edward W. (Highland Park, IL)

    1986-01-01T23:59:59.000Z

    Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture through a polymeric membrane. The membrane which is utilized to effect the separation comprises a polymer which is capable of maintaining its integrity in the presence of hydrocarbon compounds and which has been modified by being subjected to the action of a sulfonating agent. Sulfonating agents which may be employed will include fuming sulfuric acid, chlorosulfonic acid, sulfur trioxide, etc., the surface or bulk modified polymer will contain a degree of sulfonation ranging from about 15 to about 50%. The separation process is effected at temperatures ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psig.

  8. Diffusional exchange of isotopes in a metal hydride sphere.

    SciTech Connect (OSTI)

    Wolfer, Wilhelm G.; Hamilton, John C.; James, Scott Carlton

    2011-04-01T23:59:59.000Z

    This report describes the Spherical Particle Exchange Model (SPEM), which simulates exchange of one hydrogen isotope by another hydrogen isotope in a spherical metal hydride particle. This is one of the fundamental physical processes during isotope exchange in a bed of spherical metal particles and is thus one of the key components in any comprehensive physics-based model of exchange. There are two important physical processes in the model. One is the entropy of mixing between the two isotopes; the entropy of mixing is increased by having both isotopes randomly placed at interstitial sites on the lattice and thus impedes the exchange process. The other physical process is the elastic interaction between isotope atoms on the lattice. The elastic interaction is the cause for {beta}-phase formation and is independent of the isotope species. In this report the coupled diffusion equations for two isotopes in the {beta}-phase hydride are solved. A key concept is that the diffusion of one isotope depends not only on its concentration gradient, but also on the concentration gradient of the other isotope. Diffusion rate constants and the chemical potentials for deuterium and hydrogen in the {beta}-phase hydride are reviewed because these quantities are essential for an accurate model of the diffusion process. Finally, a summary of some of the predictions from the SPEM model are provided.

  9. Isotope effect evidence for the zinc hydroxide mechanism of carbonic anhydrase catalyst

    SciTech Connect (OSTI)

    Paneth, P.; O'Leary, M.H.

    1987-03-24T23:59:59.000Z

    The carbon kinetic isotope effect on the enzymatic dehydration of HCO/sub 3//sup -/ ion is k/sup 12//k/sup 13/ = 1.011 and is independent, within experimental error, of the addition of sucrose, substitution of D/sub 2/O for H/sub 2/O, and substitution of enzyme-bound Zn/sup 2 +/ by Co/sup 2 +/. These results are consistent with a ping-pong mechanism in which proton transfer between enzyme and solvent is separated from HCO/sub 3//sup -/ dehydration. For the dehydration half-reaction, diffusional processes are severalfold faster than dehydration, and the rate-determining step is the dehydration itself. The intrinsic isotope effect is approximately 1.011, indicating that hydration of CO/sub 2/ occurs by reaction of zinc-bound OH/sup -/, rather than zinc-bound H/sub 2/O.

  10. Isotope effect evidence for the zinc hydroxide mechanism of carbonic anhydrase catalysis

    SciTech Connect (OSTI)

    Paneth, P.; O'Leary, M.H.

    1987-03-24T23:59:59.000Z

    The carbon kinetic isotope effect on the enzymatic dehydration of HCO/sub 3/- ion is k12/k13 = 1.011 and is independent, within experimental error, of the addition of sucrose, substitution of D/sub 2/O for H/sub 2/O, and substitution of enzyme-bound Zn/sup 2 +/ by Co/sup 2 +/. These results are consistent with a ping-pong mechanism in which proton transfer between enzyme and solvent is separated from HCO/sub 3/- dehydration. For the dehydration half-reaction, diffusional processes are severalfold faster than dehydration, and the rate-determining step is the dehydration itself. The intrinsic isotope effect is approximately 1.011, indicating that hydration of CO/sub 2/ occurs by reaction of zinc-bound OH-, rather than zinc-bound H/sub 2/O.

  11. Advanced Separation Consortium

    SciTech Connect (OSTI)

    NONE

    2006-01-01T23:59:59.000Z

    The Center for Advanced Separation Technologies (CAST) was formed in 2001 under the sponsorship of the US Department of Energy to conduct fundamental research in advanced separation and to develop technologies that can be used to produce coal and minerals in an efficient and environmentally acceptable manner. The CAST consortium consists of seven universities - Virginia Tech, West Virginia University, University of Kentucky, Montana Tech, University of Utah, University of Nevada-Reno, and New Mexico Tech. The consortium brings together a broad range of expertise to solve problems facing the US coal industry and the mining sector in general. At present, a total of 60 research projects are under way. The article outlines some of these, on topics including innovative dewatering technologies, removal of mercury and other impurities, and modelling of the flotation process. 1 photo.

  12. Separators - Technology review: Ceramic based separators for secondary batteries

    SciTech Connect (OSTI)

    Nestler, Tina; Schmid, Robert; Münchgesang, Wolfram; Bazhenov, Vasilii; Meyer, Dirk C. [Technische Universität Bergakademie Freiberg, Institut für Experimentelle Physik, Leipziger Str. 23, 09596 Freiberg (Germany); Schilm, Jochen [Fraunhofer-Institut für Keramische Technologien und Systeme IKTS, Winterbergstraße 28, 01277 Dresden (Germany); Leisegang, Tilmann [Fraunhofer-Technologiezentrum Halbleitermaterialien THM, Am St.-Niclas-Schacht 13, 09599 Freiberg (Germany)

    2014-06-16T23:59:59.000Z

    Besides a continuous increase of the worldwide use of electricity, the electric energy storage technology market is a growing sector. At the latest since the German energy transition ('Energiewende') was announced, technological solutions for the storage of renewable energy have been intensively studied. Storage technologies in various forms are commercially available. A widespread technology is the electrochemical cell. Here the cost per kWh, e. g. determined by energy density, production process and cycle life, is of main interest. Commonly, an electrochemical cell consists of an anode and a cathode that are separated by an ion permeable or ion conductive membrane - the separator - as one of the main components. Many applications use polymeric separators whose pores are filled with liquid electrolyte, providing high power densities. However, problems arise from different failure mechanisms during cell operation, which can affect the integrity and functionality of these separators. In the case of excessive heating or mechanical damage, the polymeric separators become an incalculable security risk. Furthermore, the growth of metallic dendrites between the electrodes leads to unwanted short circuits. In order to minimize these risks, temperature stable and non-flammable ceramic particles can be added, forming so-called composite separators. Full ceramic separators, in turn, are currently commercially used only for high-temperature operation systems, due to their comparably low ion conductivity at room temperature. However, as security and lifetime demands increase, these materials turn into focus also for future room temperature applications. Hence, growing research effort is being spent on the improvement of the ion conductivity of these ceramic solid electrolyte materials, acting as separator and electrolyte at the same time. Starting with a short overview of available separator technologies and the separator market, this review focuses on ceramic-based separators. Two prominent examples, the lithium-ion and sodium-sulfur battery, are described to show the current stage of development. New routes are presented as promising technologies for safe and long-life electrochemical storage cells.

  13. System and method for high precision isotope ratio destructive analysis

    DOE Patents [OSTI]

    Bushaw, Bruce A; Anheier, Norman C; Phillips, Jon R

    2013-07-02T23:59:59.000Z

    A system and process are disclosed that provide high accuracy and high precision destructive analysis measurements for isotope ratio determination of relative isotope abundance distributions in liquids, solids, and particulate samples. The invention utilizes a collinear probe beam to interrogate a laser ablated plume. This invention provides enhanced single-shot detection sensitivity approaching the femtogram range, and isotope ratios that can be determined at approximately 1% or better precision and accuracy (relative standard deviation).

  14. Stable isotope enrichment

    ScienceCinema (OSTI)

    Egle, Brian

    2014-07-15T23:59:59.000Z

    Brian Egle is working to increase the nation's capacity to produce stable isotopes for use including medicine, industry and national security.

  15. Isotopically controlled semiconductors

    E-Print Network [OSTI]

    Haller, E.E.

    2004-01-01T23:59:59.000Z

    and phonons in semiconductors,” J. Non-Cryst. Solids 141 (LVM) Spectroscopy of Semiconductors,” Mat. Res. Soc. Symp.Isotopically Engineered Semiconductors – New Media for the

  16. Stable isotope enrichment

    SciTech Connect (OSTI)

    Egle, Brian

    2014-07-14T23:59:59.000Z

    Brian Egle is working to increase the nation's capacity to produce stable isotopes for use including medicine, industry and national security.

  17. Preliminary flowsheet: Ion exchange process for the separation of cesium from Hanford tank waste using Duolite{trademark} CS-100 resin

    SciTech Connect (OSTI)

    Eager, K.M.; Penwell, D.L.; Knutson, B.J.

    1994-12-01T23:59:59.000Z

    This preliminary flowsheet document describes an ion exchange process which uses Duolite{trademark} CS-100 resin to remove cesium from Hanford Tank waste. The flowsheet describes one possible equipment configuration, and contains mass balances based on that configuration with feeds of Neutralized Current Acid Waste, and Double Shell Slurry Feed. Process alternatives, unresolved issues, and development needs are discussed which relate to the process.

  18. Discovery of the Tungsten Isotopes

    E-Print Network [OSTI]

    A. Fritsch; J. Q. Ginepro; M. Heim; A. Schuh; A. Shore; M. Thoennessen

    2009-03-25T23:59:59.000Z

    Thirty-five tungsten isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  19. Discovery of the Titanium Isotopes

    E-Print Network [OSTI]

    D. Meierfrankenfeld; M. Thoennessen

    2010-09-08T23:59:59.000Z

    Twentyfive titanium isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  20. Discovery of the Tin Isotopes

    E-Print Network [OSTI]

    S. Amos; M. Thoennessen

    2010-09-08T23:59:59.000Z

    Thirty-eight tin isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  1. Discovery of the tungsten isotopes

    SciTech Connect (OSTI)

    Fritsch, A.; Ginepro, J.Q.; Heim, M.; Schuh, A.; Shore, A. [National Superconducting Cyclotron Laboratory and Department of Physics and Astronomy, Michigan State University, East Lansing, MI 48824 (United States); Thoennessen, M. [National Superconducting Cyclotron Laboratory and Department of Physics and Astronomy, Michigan State University, East Lansing, MI 48824 (United States)], E-mail: thoennessen@nscl.msu.edu

    2010-05-15T23:59:59.000Z

    Thirty-five tungsten isotopes have been observed so far and the discovery of these isotopes is discussed here. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  2. Discovery of the Tungsten Isotopes

    E-Print Network [OSTI]

    Fritsch, A; Heim, M; Schuh, A; Shore, A; Thoennessen, M

    2009-01-01T23:59:59.000Z

    Thirty-five tungsten isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  3. Resolving the stellar sources of isotopically rare presolar silicate grains through Mg and Fe isotopic analyses

    SciTech Connect (OSTI)

    Nguyen, Ann N.; Messenger, Scott, E-mail: lan-anh.n.nguyen@nasa.gov [Robert M. Walker Laboratory for Space Science, Astromaterials Research and Exploration Science Directorate, NASA Johnson Space Center, Houston, TX 77058 (United States)

    2014-04-01T23:59:59.000Z

    We conducted multi-element isotopic analyses of 11 presolar silicate grains from the Acfer 094 meteorite having unusual O isotopic compositions. Eight grains are {sup 18}O-rich, one is {sup 16}O-rich, and two are extremely {sup 17}O-rich. We constrained the grains' stellar sources by measuring their Si and Mg isotopic ratios, and also the {sup 54}Fe/{sup 56}Fe and {sup 57}Fe/{sup 56}Fe ratios for five grains. The Mg and Fe isotopic measurements were conducted after surrounding matrix grains were removed for more accurate ratios. Most of the {sup 18}O-rich silicates had anomalous Mg isotopic ratios, and their combined isotopic constraints are consistent with origins in low-mass Type II supernovae (SNe II) rather than high-metallicity stars. The isotopic ratios of the {sup 16}O-rich silicate are also consistent with an SN origin. Mixing small amounts of interior stellar material with the stellar envelope replicated all measured isotopic ratios except for {sup 29}Si/{sup 28}Si and {sup 54}Fe/{sup 56}Fe in some grains. The {sup 29}Si/{sup 28}Si ratios of all SN-derived grains are matched by doubling the {sup 29}Si yield in the Ne- and Si-burning zones. The {sup 54}Fe/{sup 56}Fe ratios of the grains imply elemental fractionation in the Si/S zone, or introduction of isotopically solar Fe by secondary processing. The two highly {sup 17}O-rich silicates exhibited significant {sup 25}Mg and/or {sup 26}Mg enrichments and their isotopic ratios are best explained by strong dilution of 1.15 M {sub ?} CO nova matter. We estimate that ?12% and 1% of presolar silicates have SN and nova origins, respectively, similar to presolar SiC and oxides. This implies that asymptotic giant branch stars are the dominant dust producers in the galaxy.

  4. Elemental and isotopic separation by diffusion in geological liquids

    E-Print Network [OSTI]

    Watkins, James Mervin

    2010-01-01T23:59:59.000Z

    J. , 1974. Igneous Petrology. McGraw-Hill, New York, 739to Mineralogy and Petrology 101, Newman, S. , Stolper, E. ,Contributions to Mineralogy and Petrology 80, 83–87. Watson,

  5. Y-12 plant prepares to separate lithium isotopes

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    patterned after "Fat Man," because the Soviets were now on equal footing with a thermonuclear weapon capability -- and Y-12 was charged with increasing production and adapting...

  6. Packed bed reactor for photochemical .sup.196 Hg isotope separation

    DOE Patents [OSTI]

    Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA)

    1992-01-01T23:59:59.000Z

    Straight tubes and randomly oriented pieces of tubing having been employed in a photochemical mercury enrichment reactor and have been found to improve the enrichment factor (E) and utilization (U) compared to a non-packed reactor. One preferred embodiment of this system uses a moving bed (via gravity) for random packing.

  7. Mantle Helium And Carbon Isotopes In Separation Creek Geothermal Springs,

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov YouKizildere I Geothermal Pwer Plant Jump to:LandownersLuther,Jemez PuebloManteca, California: Energy Resources Jump

  8. (Carbon isotope fractionation inplants)

    SciTech Connect (OSTI)

    O'Leary, M.H.

    1990-01-01T23:59:59.000Z

    The objectives of this research are: To develop a theoretical and experimental framework for understanding isotope fractionations in plants; and to develop methods for using this isotope fractionation for understanding the dynamics of CO{sub 2} fixation in plants. Progress is described.

  9. Analytical Validation of Accelerator Mass Spectrometry for Pharmaceutical Development: the Measurement of Carbon-14 Isotope Ratio.

    SciTech Connect (OSTI)

    Keck, B D; Ognibene, T; Vogel, J S

    2010-02-05T23:59:59.000Z

    Accelerator mass spectrometry (AMS) is an isotope based measurement technology that utilizes carbon-14 labeled compounds in the pharmaceutical development process to measure compounds at very low concentrations, empowers microdosing as an investigational tool, and extends the utility of {sup 14}C labeled compounds to dramatically lower levels. It is a form of isotope ratio mass spectrometry that can provide either measurements of total compound equivalents or, when coupled to separation technology such as chromatography, quantitation of specific compounds. The properties of AMS as a measurement technique are investigated here, and the parameters of method validation are shown. AMS, independent of any separation technique to which it may be coupled, is shown to be accurate, linear, precise, and robust. As the sensitivity and universality of AMS is constantly being explored and expanded, this work underpins many areas of pharmaceutical development including drug metabolism as well as absorption, distribution and excretion of pharmaceutical compounds as a fundamental step in drug development. The validation parameters for pharmaceutical analyses were examined for the accelerator mass spectrometry measurement of {sup 14}C/C ratio, independent of chemical separation procedures. The isotope ratio measurement was specific (owing to the {sup 14}C label), stable across samples storage conditions for at least one year, linear over 4 orders of magnitude with an analytical range from one tenth Modern to at least 2000 Modern (instrument specific). Further, accuracy was excellent between 1 and 3 percent while precision expressed as coefficient of variation is between 1 and 6% determined primarily by radiocarbon content and the time spent analyzing a sample. Sensitivity, expressed as LOD and LLOQ was 1 and 10 attomoles of carbon-14 (which can be expressed as compound equivalents) and for a typical small molecule labeled at 10% incorporated with {sup 14}C corresponds to 30 fg equivalents. AMS provides an sensitive, accurate and precise method of measuring drug compounds in biological matrices.

  10. Understanding denitrification with stable isotope measurements of N2: proof of concept study

    E-Print Network [OSTI]

    Downer, Roswell Curtis

    2004-01-01T23:59:59.000Z

    The biologically mediated removal of nitrogen from estuarine and shallow coastal waters was investigated using a new method for the determination of N? isotope ratios. This method employs the use of a chromatographic separation technique to purify...

  11. Utilization of kinetic isotope effects for the concentration of tritium. 1997 annual progress report

    SciTech Connect (OSTI)

    Brown, G.M.; Meyer, T.J.

    1997-09-01T23:59:59.000Z

    'The objective of this research program is to develop methods for concentrating tritium in water based on large primary isotope effects in catalytic redox processes. Basic research is being conducted to develop the chemistry of a complete cyclic process. Because tritium [generally present as tritiated water (HTO)] is in a rapidly established equilibrium with water, it moves with groundwater and separation from water cannot be achieved by the usual pump-and-treat methods using sorbents. The general methodology developed in this work will be applicable to a number of US Department of Energy waste streams, and as a consequence of the process, tritium could be incorporated in an organic polymer, a form that will prevent its ready transport in groundwater.'

  12. Iodine-129 separation and determination by neutron activation analysis

    SciTech Connect (OSTI)

    Bate, L.C.; Stokely, J.R.

    1981-01-01T23:59:59.000Z

    A method is described for analysis of /sup 129/I in fission product mixtures originating from fuel reprocessing studies and low-level wastes. The method utilizes conventional iodine valence adjustment and solvent extraction techniques to chemically separate /sup 129/I from most fission products. The /sup 129/I is determined by neutron irradiation and measurement of the 12.4 h /sup 130/I produced by the neutron capture reaction. Special techniques were devised for neutron irradiation of /sup 129/I samples in the pneumatic tube irradiation facilities at the High Flux Isotope (HFIR) and Oak Ridge Research (ORR) Reactors. Chemically separated /sup 129/I is adsorbed on an anion exchange resin column made from an irradiation container. The loaded resin is then irradiated in either of the pneumatic facilities to produce /sup 130/I. Sensitivity of the analysis with the HFIR facility (flux: 5 x 10/sup 14/ n/cm/sup 2//sec) and a 100-second irradiation time is approximately 0.03 nanograms. Samples up to 250 ml in volume can be easily processed.

  13. Isotopic Scaling in Nuclear Reactions

    E-Print Network [OSTI]

    M. B. Tsang; W. A. Friedman; C. K. Gelbke; W. G. Lynch; G. Verde; H. Xu

    2001-03-26T23:59:59.000Z

    A three parameter scaling relationship between isotopic distributions for elements with Z$\\leq 8$ has been observed that allows a simple description of the dependence of such distributions on the overall isospin of the system. This scaling law (termed iso-scaling) applies for a variety of reaction mechanisms that are dominated by phase space, including evaporation, multifragmentation and deeply inelastic scattering. The origins of this scaling behavior for the various reaction mechanisms are explained. For multifragmentation processes, the systematics is influenced by the density dependence of the asymmetry term of the equation of state.

  14. Enhanced membrane gas separations

    SciTech Connect (OSTI)

    Prasad, R.

    1993-07-13T23:59:59.000Z

    An improved membrane gas separation process is described comprising: (a) passing a feed gas stream to the non-permeate side of a membrane system adapted for the passage of purge gas on the permeate side thereof, and for the passage of the feed gas stream in a counter current flow pattern relative to the flow of purge gas on the permeate side thereof, said membrane system being capable of selectively permeating a fast permeating component from said feed gas, at a feed gas pressure at or above atmospheric pressure; (b) passing purge gas to the permeate side of the membrane system in counter current flow to the flow of said feed gas stream in order to facilitate carrying away of said fast permeating component from the surface of the membrane and maintaining the driving force for removal of the fast permeating component through the membrane from the feed gas stream, said permeate side of the membrane being maintained at a subatmospheric pressure within the range of from about 0.1 to about 5 psia by vacuum pump means; (c) recovering a product gas stream from the non-permeate side of the membrane; and (d) discharging purge gas and the fast permeating component that has permeated the membrane from the permeate side of the membrane, whereby the vacuum conditions maintained on the permeate side of the membrane by said vacuum pump means enhance the efficiency of the gas separation operation, thereby reducing the overall energy requirements thereof.

  15. System for recovery of daughter isotopes from a source material

    SciTech Connect (OSTI)

    Tranter, Troy J. (Idaho Falls, ID) [Idaho Falls, ID; Todd, Terry A. (Aberdeen, ID) [Aberdeen, ID; Lewis, Leroy C. (Idaho Falls, ID) [Idaho Falls, ID; Henscheid, Joseph P. (Idaho Falls, ID) [Idaho Falls, ID

    2009-08-04T23:59:59.000Z

    A method of separating isotopes from a mixture containing at least two isotopes in a solution is disclosed. A first isotope is precipitated and is collected from the solution. A daughter isotope is generated and collected from the first isotope. The invention includes a method of producing an actinium-225/bismuth-213 product from a material containing thorium-229 and thorium-232. A solution is formed containing nitric acid and the material containing thorium-229 and thorium-232, and iodate is added to form a thorium iodate precipitate. A supernatant is separated from the thorium iodate precipitate and a second volume of nitric acid is added to the thorium iodate precipitate. The thorium iodate precipitate is stored and a decay product comprising actinium-225 and bismuth-213 is generated in the second volume of nitric acid, which is then separated from the thorium iodate precipitate, filtered, and treated using at least one chromatographic procedure. A system for producing an actinium-225/bismuth-213 product is also disclosed.

  16. 33rd Actinide Separations Conference

    SciTech Connect (OSTI)

    McDonald, L M; Wilk, P A

    2009-05-04T23:59:59.000Z

    Welcome to the 33rd Actinide Separations Conference hosted this year by the Lawrence Livermore National Laboratory. This annual conference is centered on the idea of networking and communication with scientists from throughout the United States, Britain, France and Japan who have expertise in nuclear material processing. This conference forum provides an excellent opportunity for bringing together experts in the fields of chemistry, nuclear and chemical engineering, and actinide processing to present and discuss experiences, research results, testing and application of actinide separation processes. The exchange of information that will take place between you, and other subject matter experts from around the nation and across the international boundaries, is a critical tool to assist in solving both national and international problems associated with the processing of nuclear materials used for both defense and energy purposes, as well as for the safe disposition of excess nuclear material. Granlibakken is a dedicated conference facility and training campus that is set up to provide the venue that supports communication between scientists and engineers attending the 33rd Actinide Separations Conference. We believe that you will find that Granlibakken and the Lake Tahoe views provide an atmosphere that is stimulating for fruitful discussions between participants from both government and private industry. We thank the Lawrence Livermore National Laboratory and the United States Department of Energy for their support of this conference. We especially thank you, the participants and subject matter experts, for your involvement in the 33rd Actinide Separations Conference.

  17. Separation of contributions from deeply virtual Compton scattering and its interference with the Bethe--Heitler process in measurements on a hydrogen target

    E-Print Network [OSTI]

    The HERMES collaboration; A. Airapetian

    2009-09-19T23:59:59.000Z

    Hard exclusive leptoproduction of real photons from an unpolarized proton target is studied in an effort to elucidate generalized parton distributions. The data accumulated during the years 1996--2005 with the HERMES spectrometer are analyzed to yield asymmetries with respect to the combined dependence of the cross section on beam helicity and charge, thereby revealing previously unseparated contributions from deeply virtual Compton scattering and its interference with the Bethe--Heitler process. The integrated luminosity is sufficient to show correlated dependences on two kinematic variables, and provides the most precise determination of the dependence on only the beam charge.

  18. High-purity, isotopically enriched bulk silicon

    E-Print Network [OSTI]

    2004-01-01T23:59:59.000Z

    Russia. The stated isotope enrichments are summarized inenrichments >99% have been achieved for each isotope andthe enrichment is highest, are presented. isotope at. % nat.

  19. Atomic line emission analyzer for hydrogen isotopes

    DOE Patents [OSTI]

    Kronberg, J.W.

    1991-05-08T23:59:59.000Z

    Apparatus for isotopic analysis of hydrogen comprises a low pressure chamber into which a sample of hydrogen is introduced and then exposed to an electrical discharge to excite the electrons of the hydrogen atoms to higher energy states and thereby cause the emission of light on the return to lower energy states, a Fresnel prism made at least in part of a material anomalously dispersive to the wavelengths of interest for dispersing the emitted light, and a photodiode array for receiving the dispersed light. The light emitted by the sample is filtered to pass only the desired wavelengths, such as one of the lines of the Balmer series for hydrogen, the wavelengths of which differ slightly from one isotope to another. The output of the photodiode array is processed to determine the relative amounts of each isotope present in the sample. Additionally, the sample itself may be recovered using, a metal hydride.

  20. Atomic line emission analyzer for hydrogen isotopes

    DOE Patents [OSTI]

    Kronberg, James W. (108 Independent Blvd., Aiken, SC 29801)

    1993-01-01T23:59:59.000Z

    Apparatus for isotopic analysis of hydrogen comprises a low pressure chamber into which a sample of hydrogen is introduced and then exposed to an electrical discharge to excite the electrons of the hydrogen atoms to higher energy states and thereby cause the emission of light on the return to lower energy states, a Fresnel prism made at least in part of a material anomalously dispersive to the wavelengths of interest for dispersing the emitted light, and a photodiode array for receiving the dispersed light. The light emitted by the sample is filtered to pass only the desired wavelengths, such as one of the lines of the Balmer series for hydrogen, the wavelengths of which differ slightly from one isotope to another. The output of the photodiode array is processed to determine the relative amounts of each isotope present in the sample. Additionally, the sample itself may be recovered using a metal hydride.

  1. Atomic line emission analyzer for hydrogen isotopes

    DOE Patents [OSTI]

    Kronberg, J.W.

    1993-03-30T23:59:59.000Z

    Apparatus for isotopic analysis of hydrogen comprises a low pressure chamber into which a sample of hydrogen is introduced and then exposed to an electrical discharge to excite the electrons of the hydrogen atoms to higher energy states and thereby cause the emission of light on the return to lower energy states, a Fresnel prism made at least in part of a material anomalously dispersive to the wavelengths of interest for dispersing the emitted light, and a photodiode array for receiving the dispersed light. The light emitted by the sample is filtered to pass only the desired wavelengths, such as one of the lines of the Balmer series for hydrogen, the wavelengths of which differ slightly from one isotope to another. The output of the photodiode array is processed to determine the relative amounts of each isotope present in the sample. Additionally, the sample itself may be recovered using a metal hydride.

  2. Transportation of medical isotopes

    SciTech Connect (OSTI)

    Nielsen, D.L.

    1997-11-19T23:59:59.000Z

    A Draft Technical Information Document (HNF-1855) is being prepared to evaluate proposed interim tritium and medical isotope production at the Fast Flux Test Facility (FFTF). This assessment examines the potential health and safety impacts of transportation operations associated with the production of medical isotopes. Incident-free and accidental impacts are assessed using bounding source terms for the shipment of nonradiological target materials to the Hanford Site, the shipment of irradiated targets from the FFTF to the 325 Building, and the shipment of medical isotope products from the 325 Building to medical distributors. The health and safety consequences to workers and the public from the incident-free transportation of targets and isotope products would be within acceptable levels. For transportation accidents, risks to works and the public also would be within acceptable levels. This assessment is based on best information available at this time. As the medical isotope program matures, this analysis will be revised, if necessary, to support development of a final revision to the Technical Information Document.

  3. Development of Improved Sorbents for Radiochemical Separations at the SRS

    SciTech Connect (OSTI)

    HOBBS, DAVID

    2005-01-20T23:59:59.000Z

    High-level nuclear waste produced from fuel reprocessing operations at the Savannah River Site (SRS) requires pretreatment to remove Cs-137, Sr-90 and alpha-emitting radionuclides (i.e., actinides) prior to disposal. Separation processes planned at SRS include caustic side solvent extraction, for Cs-137 removal, and ion exchange/sorption of Sr-90 and alpha-emitting radionuclides with monosodium titanate (MST). The predominant alpha-emitting radionuclides in the highly alkaline waste solutions include plutonium isotopes Pu-238, Pu-239 and Pu-240. This paper describes results from a project funded by the U.S. Department of Energy Office of Cleanup Technology to produce sorbents that exhibit increased removal kinetics and capacity for Sr-90 and alpha-emitting radionuclides versus that of the baseline MST material. Testing indicated that MST samples prepared in the presence of organic-based templating reagents showed limited improvements in performance compared to the baseline MST. We observed significantly improved plutonium and neptunium removal performance with MST samples prepared upon the addition of a proprietary reagent. The modified MST offers the possibility of increased throughput and reduced solids handling in waste processing facilities at the SRS.

  4. Photolytic Processes

    Broader source: Energy.gov [DOE]

    Photolytic processes use the energy in sunlight to separate water into hydrogen and oxygen. These processes are in the very early stages of research but offer long-term potential for sustainable...

  5. 7, 1271512750, 2007 Hydrogen isotope

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    imply that there must be a very strong concomitant isotopic enrichment in the radical channel (CH2O + hACPD 7, 12715­12750, 2007 Hydrogen isotope fractionation in the photolysis of formaldehyde T. S a Creative Commons License. Atmospheric Chemistry and Physics Discussions Hydrogen isotope fractionation

  6. Separation of polar gases from nonpolar gases

    DOE Patents [OSTI]

    Kulprathipanja, Santi (Hoffman Estates, IL); Kulkarni, Sudhir S. (Hoffman Estates, IL)

    1986-01-01T23:59:59.000Z

    Polar gases such as hydrogen sulfide, sulfur dioxide and ammonia may be separated from nonpolar gases such as methane, nitrogen, hydrogen or carbon dioxide by passing a mixture of polar and nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The use of such membranes as exemplified by polyethylene glycol and silicon rubber composited on polysulfone will permit greater selectivity accompanied by a high flux rate in the separation process.

  7. Separation of polar gases from nonpolar gases

    DOE Patents [OSTI]

    Kulprathipanja, S.; Kulkarni, S.S.

    1986-08-26T23:59:59.000Z

    Polar gases such as hydrogen sulfide, sulfur dioxide and ammonia may be separated from nonpolar gases such as methane, nitrogen, hydrogen or carbon dioxide by passing a mixture of polar and nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The use of such membranes as exemplified by polyethylene glycol and silicon rubber composited on polysulfone will permit greater selectivity accompanied by a high flux rate in the separation process.

  8. Voluntary Separation Programs

    Broader source: Energy.gov (indexed) [DOE]

    than that to which the employee would otherwise be entitled upon separation from employment. Waivers are mandatory bargaining subjects. Therefore, if the affected employees are...

  9. Organic contaminant separator

    DOE Patents [OSTI]

    Del Mar, P.

    1993-12-28T23:59:59.000Z

    A process is presented of sample preparation prior to analysis for the concentration of an organic contaminant in an aqueous medium by (a) passing an initial aqueous medium including a minor amount of the organic contaminant through a composite tube comprised of a blend of a polyolefin and a polyester, the composite tube having an internal diameter of from about 0.1 to about 2.0 millimeters and being of sufficient length to permit the organic contaminant to adhere to the composite tube, (b) passing a solvent through the composite tube. The solvent is capable of separating the adhered organic contaminant from the composite tube. Further, an extraction apparatus is presented for sample preparation prior to analysis for the concentration of an organic contaminant in an aqueous medium. The apparatus includes a composite tube comprised of a blend of a polyolefin and a polyester. The composite tube has an internal diameter of from about 0.1 to about 2.0 millimeters and has sufficient length to permit an organic contaminant contained within an aqueous medium passed therethrough to adhere to the composite tube. 2 figures.

  10. Radiochemical Separation & Processing | ornl.gov

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    of future NASA deep space missions. Building 7930 was originally constructed for thorium fuel cycle research but it was never used for this purpose. It is a three-level,...

  11. HF separation in a carbonylation process

    SciTech Connect (OSTI)

    Grote, D.; Trivedi, B.C.; Mason, T.O.

    1987-04-28T23:59:59.000Z

    This patent describes the carbonylation of an olefin with carbon monoxide in the presence of hydrogen fluoride catalyst wherein the reaction product is treated with water to produce a mixture of a carboxylic acid, HF and optionally water. The improvement comprises contacting at a temperature in the range of from about 25/sup 0/C up to about 100/sup 0/C, the mixture with one side of a cation permeable membrane of a copolymer of tetrafluoro ethylene and perfluoro-3, 6-dioxa-4-methyl-octen sulfamic acid whose other side is in contact with water.

  12. Development of an Algal Oil Separation Process

    E-Print Network [OSTI]

    Samarasinghe, Nalin

    2012-10-19T23:59:59.000Z

    for quantification of algal cell disruption induced by homogenization. The selected method, hemocytometry was used to measure the degree of algal cell disruption induced by homogenization. In the third section, various homogenization treatments were evaluated...

  13. Radiochemical Separation & Processing | ornl.gov

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level:Energy: Grid Integration Redefining What's PossibleRadiation Protection Radiation Protection Regulations: TheCompetition »Radiochemical

  14. Physics of Aquatic Systems II, 3. Stable Isotopes -Theory Universitt HeidelbergInstitut fr Umweltphysik Physics of Aquatic Systems II

    E-Print Network [OSTI]

    Aeschbach-Hertig, Werner

    ­ Notation and definitions ­ Origin and description of fractionation ­ Fractionating processes ­ Rayleigh distillation Literature: Mook Vol. I, ch. 3 and 4 Physics of Aquatic Systems II, 3. Stable Isotopes - Theory "concentration" or mixing ratio: Fractional abundance of given isotope relative to all isotopes of the element

  15. Extraction of gadolinium from high flux isotope reactor control plates. [Alternative method

    SciTech Connect (OSTI)

    Kohring, M.W.

    1987-04-01T23:59:59.000Z

    Gadolinium-153 is an important radioisotope used in the diagnosis of various bone disorders. Recent medical and technical developments in the detection and cure of osteoporosis, a bone disease affecting an estimated 50 million people, have greatly increased the demand for this isotope. The Oak Ridge National Laboratory (ORNL) has produced /sup 153/Gd since 1980 primarily through the irradiation of a natural europium-oxide powder followed by the chemical separation of the gadolinium fraction from the europium material. Due to the higher demand for /sup 153/Gd, an alternative production method to supplement this process has been investigated. This process involves the extraction of gadolinium from the europium-bearing region of highly radioactive, spent control plates used at the High Flux Isotope Reactor (HFIR) with a subsequent re-irradiation of the extracted material for the production of the /sup 153/Gd. Based on the results of experimental and calculational analyses, up to 25 grams of valuable gadolinium (greater than or equal to60% enriched in /sup 152/Gd) resides in the europium-bearing region of the HFIR control components of which 70% is recoverable. At a specific activity yield of 40 curies of /sup 153/Gd for each gram of gadolinium re-irradiated, 700 one-curie sources can be produced from each control plate assayed.

  16. Understand the potential of electro-separations

    SciTech Connect (OSTI)

    Byers, C.H. (Oak Ridge National Lab., TN (United States)); Amarnath, A. (Electric Power Research Inst., Palo Alto, CA (United States))

    1995-02-01T23:59:59.000Z

    Unit operations to separate and purify chemicals consume over 4 Quads (10[sup 15] Btu) of energy in the US alone each year. They also directly or indirectly generate considerable amounts of emissions. These economic and environmental pressures pose challenges that will require new processing approaches. The authors feel that electro-separations will play a leading role in achieving the efficiency and environmental improvements that will be demanded of the chemical process industries (CPI) in the early 21st Century. In this article, the authors provide an overview of the status of electro-separations. But first, to avoid any confusion, they clarify what they mean by the term electro-separations. Conventionally, it refers only to electrolysis-type technologies, such as electrophoresis, electrokinetics, and electrodialysis. Instead, they propose a broader definition: the use of electricity, or electro-magnetic fields to produce and enhance chemical or physical separation. The definition thus includes such processes as electro- and dielectric filtration, magnetic separation, any process where electric or magnetic fields profoundly affect the transport rate, and numerous other technologies that are now in early development but, with adequate support, may become preeminent separation technologies. The relative significance of this broad palette of technologies to the emerging needs of the CPI is the subject of their ongoing study.

  17. Separators for flywheel rotors

    DOE Patents [OSTI]

    Bender, D.A.; Kuklo, T.C.

    1998-07-07T23:59:59.000Z

    A separator forms a connection between the rotors of a concentric rotor assembly. This separator allows for the relatively free expansion of outer rotors away from inner rotors while providing a connection between the rotors that is strong enough to prevent disassembly. The rotor assembly includes at least two rotors referred to as inner and outer flywheel rings or rotors. This combination of inner flywheel ring, separator, and outer flywheel ring may be nested to include an arbitrary number of concentric rings. The separator may be a segmented or continuous ring that abuts the ends of the inner rotor and the inner bore of the outer rotor. It is supported against centrifugal loads by the outer rotor and is affixed to the outer rotor. The separator is allowed to slide with respect to the inner rotor. It is made of a material that has a modulus of elasticity that is lower than that of the rotors. 10 figs.

  18. Separators for flywheel rotors

    DOE Patents [OSTI]

    Bender, Donald A. (Dublin, CA); Kuklo, Thomas C. (Oakdale, CA)

    1998-01-01T23:59:59.000Z

    A separator forms a connection between the rotors of a concentric rotor assembly. This separator allows for the relatively free expansion of outer rotors away from inner rotors while providing a connection between the rotors that is strong enough to prevent disassembly. The rotor assembly includes at least two rotors referred to as inner and outer flywheel rings or rotors. This combination of inner flywheel ring, separator, and outer flywheel ring may be nested to include an arbitrary number of concentric rings. The separator may be a segmented or continuous ring that abuts the ends of the inner rotor and the inner bore of the outer rotor. It is supported against centrifugal loads by the outer rotor and is affixed to the outer rotor. The separator is allowed to slide with respect to the inner rotor. It is made of a material that has a modulus of elasticity that is lower than that of the rotors.

  19. Stable Isotope Protocols: Sampling and Sample Processing

    E-Print Network [OSTI]

    Levin, Lisa A; Currin, Carolyn

    2012-01-01T23:59:59.000Z

    have used “rings”, made of either PVC pipe or styrofoam (forbands to hold screen onto PVC sections). This techniquestore BMI vm, dc “Rings”-PVC >8” diameter Hardware store BMI

  20. Stable Isotope Protocols: Sampling and Sample Processing

    E-Print Network [OSTI]

    Levin, Lisa A; Currin, Carolyn

    2012-01-01T23:59:59.000Z

    supply Co. All Table Top Centrifuge Scientific supply co.to 15 ml of distilled water in a 50 ml centrifuge tube.Stir, shake vigorously, and centrifuge at speed 6 for 5 min.

  1. Gas Separations using Ceramic Membranes

    SciTech Connect (OSTI)

    Paul KT Liu

    2005-01-13T23:59:59.000Z

    This project has been oriented toward the development of a commercially viable ceramic membrane for high temperature gas separations. A technically and commercially viable high temperature gas separation membrane and process has been developed under this project. The lab and field tests have demonstrated the operational stability, both performance and material, of the gas separation thin film, deposited upon the ceramic membrane developed. This performance reliability is built upon the ceramic membrane developed under this project as a substrate for elevated temperature operation. A comprehensive product development approach has been taken to produce an economically viable ceramic substrate, gas selective thin film and the module required to house the innovative membranes for the elevated temperature operation. Field tests have been performed to demonstrate the technical and commercial viability for (i) energy and water recovery from boiler flue gases, and (ii) hydrogen recovery from refinery waste streams using the membrane/module product developed under this project. Active commercializations effort teaming with key industrial OEMs and end users is currently underway for these applications. In addition, the gas separation membrane developed under this project has demonstrated its economical viability for the CO2 removal from subquality natural gas and landfill gas, although performance stability at the elevated temperature remains to be confirmed in the field.

  2. Temperature dependence of carbon isotope fractionation in CAM plants

    SciTech Connect (OSTI)

    Deleens, E.; Treichel, I.; O'Leary, M.H.

    1985-09-01T23:59:59.000Z

    The carbon isotope fractionation associated with nocturnal malic acid synthesis in Kalanchoe daigremontiana and Bryophyllum tubiflorum was calculated from the isotopic composition of carbon-4 of malic acid, after appropriate corrections. In the lowest temperature treatment (17/sup 0/C nights, 23/sup 0/C days), the isotope fractionation for both plants is -4% per thousand (that is, malate is enriched in /sup 13/C relative to the atmosphere). For K. daigremontiana, the isotope fractionation decreases with increasing temperature, becoming approximately 0% per thousand at 27/sup 0/C/33/sup 0/C. Detailed analysis of temperature effects on the isotope fractionation indicates that stomatal aperture decreases with increasing temperature and carboxylation capacity increases. For B. tubiflorum, the temperature dependence of the isotope fractionation is smaller and is principally attributed to the normal temperature dependences of the rates of diffusion and carboxylation steps. The small change in the isotopic composition of remaining malic acid in both species which is observed during deacidification indicates that malate release, rather than decarboxylation, is rate limiting in the deacidification process. 28 references, 1 figure, 4 tables.

  3. ISOTOPE METHODS IN HOMOGENEOUS CATALYSIS.

    SciTech Connect (OSTI)

    BULLOCK,R.M.; BENDER,B.R.

    2000-12-01T23:59:59.000Z

    The use of isotope labels has had a fundamentally important role in the determination of mechanisms of homogeneously catalyzed reactions. Mechanistic data is valuable since it can assist in the design and rational improvement of homogeneous catalysts. There are several ways to use isotopes in mechanistic chemistry. Isotopes can be introduced into controlled experiments and followed where they go or don't go; in this way, Libby, Calvin, Taube and others used isotopes to elucidate mechanistic pathways for very different, yet important chemistries. Another important isotope method is the study of kinetic isotope effects (KIEs) and equilibrium isotope effect (EIEs). Here the mere observation of where a label winds up is no longer enough - what matters is how much slower (or faster) a labeled molecule reacts than the unlabeled material. The most careti studies essentially involve the measurement of isotope fractionation between a reference ground state and the transition state. Thus kinetic isotope effects provide unique data unavailable from other methods, since information about the transition state of a reaction is obtained. Because getting an experimental glimpse of transition states is really tantamount to understanding catalysis, kinetic isotope effects are very powerful.

  4. Europium, Samarium, and Neodymium Isotopic Fractions in Metal-Poor Stars

    E-Print Network [OSTI]

    Ian U. Roederer; James E. Lawler; Christopher Sneden; John J. Cowan; Jennifer S. Sobeck; Catherine A. Pilachowski

    2007-12-16T23:59:59.000Z

    We have derived isotopic fractions of europium, samarium, and neodymium in two metal-poor giants with differing neutron-capture nucleosynthetic histories. These isotopic fractions were measured from new high resolution (R ~ 120,000), high signal-to-noise (S/N ~ 160-1000) spectra obtained with the 2dCoude spectrograph of McDonald Observatory's 2.7m Smith telescope. Synthetic spectra were generated using recent high-precision laboratory measurements of hyperfine and isotopic subcomponents of several transitions of these elements and matched quantitatively to the observed spectra. We interpret our isotopic fractions by the nucleosynthesis predictions of the stellar model, which reproduces s-process nucleosynthesis from the physical conditions expected in low-mass, thermally-pulsing stars on the AGB, and the classical method, which approximates s-process nucleosynthesis by a steady neutron flux impinging upon Fe-peak seed nuclei. Our Eu isotopic fraction in HD 175305 is consistent with an r-process origin by the classical method and is consistent with either an r- or an s-process origin by the stellar model. Our Sm isotopic fraction in HD 175305 suggests a predominantly r-process origin, and our Sm isotopic fraction in HD 196944 is consistent with an s-process origin. The Nd isotopic fractions, while consistent with either r-process or s-process origins, have very little ability to distinguish between any physical values for the isotopic fraction in either star. This study for the first time extends the n-capture origin of multiple rare earths in metal-poor stars from elemental abundances to the isotopic level, strengthening the r-process interpretation for HD 175305 and the s-process interpretation for HD196944.

  5. Water isotopes and the general circulation

    E-Print Network [OSTI]

    Noone, David

    is depleted. #12;Distillation: vapor and condensate Isotopic fractionation -35 -30 -25 -20 -15 -10 -5 0 5 0 0 of idealized isotopic fractionation Expression of isotopic fractionation in nature Attributing signals" 18 = (R/Rstandard-1)x1000 R = moles of H2 18O/moles of H2 16O #12;Isotopic fractionation Isotopic

  6. USABC Battery Separator Development

    Broader source: Energy.gov (indexed) [DOE]

    Separator Development P.I. - Ron Smith Presenter - Kristoffer Stokes, Ph.D. Celgard, LLC Project ID ES007 May 10, 2011 This presentation does not contain any proprietary,...

  7. Microsystem capillary separations

    DOE Patents [OSTI]

    TeGrotenhuis, Ward E [Kennewick, WA; Wegeng, Robert S [Richland, WA; Whyatt, Greg A [West Richland, WA; Stenkamp, Victoria S [Richland, WA; Gauglitz, Phillip A [Richland, WA

    2003-12-23T23:59:59.000Z

    Laminated, multiphase separators and contactors having wicking structures and gas flow channels are described. Some preferred embodiments are combined with microchannel heat exchange. Integrated systems containing these components are also part of the present invention.

  8. Molten salt electrolyte separator

    DOE Patents [OSTI]

    Kaun, Thomas D. (New Lenox, IL)

    1996-01-01T23:59:59.000Z

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

  9. Membrane Separations Research

    E-Print Network [OSTI]

    Fair, J. R.

    applicabilily of separation mel hods for the removal of carbon dioxide frum gas streams. Another application of hybrid systems deals with hydrogen recovery. As discussed earlier, this separation may be made by membrane petmeation, but classically it has also... box; altemate schemes have this sequence reversed. Sal6S gas Feed Membrane ~ Acid gas Amine conlactor Acid gas Amine stripper Figure 7. Hybrid system for the removal of acid gases from nalural gas. MEMBRANE UNIT COLD BOX HYDROGEN PRODUCT...

  10. Development of high through-put Sr isotope analysis for monitoring reservoir integrity for CO{sub 2} storage.

    SciTech Connect (OSTI)

    Wall, Andy; Jain, Jinesh; Stewart, Brian; Capo, Rosemary; Hakala, Alexandra J.; Hammack, Richard; Guthrie, George

    2012-01-01T23:59:59.000Z

    Recent innovations in multi-collector ICP-mass spectrometry (MC-ICP-MS) have allowed for rapid and precise measurements of isotope ratios in geological samples. Naturally occurring Sr isotopes has the potential for use in Monitoring, Verification, and Accounting (MVA) associated with geologic CO2 storage. Sr isotopes can be useful for: Sensitive tracking of brine migration; Determining seal rock leakage; Studying fluid/rock reactions. We have optimized separation chemistry procedures that will allow operators to prepare samples for Sr isotope analysis off site using rapid, low cost methods.

  11. Recovery of enriched stable isotopes in radionuclide production

    SciTech Connect (OSTI)

    Razbash, A.A.; Sevastyanov, Yu.G.; Polyakov, O.N.; Krasnov, N.N.; Konyakhin, N.A.; Tolstouhov, Yu.V.; Maklachkov, A.G. [Cyclotron Co. Ltd., Obninsk (Russian Federation)

    1994-12-31T23:59:59.000Z

    The wide application of radionuclides in different fields of science and industry demanded an increase of their production. One of the ways to increase the radionuclide production on present cyclotrons is the use of the targets from enriched stable isotopes. This allows one to raise the productivity in some cases by two or more times and to increase radionuclidic purity. It should be noted, however, that enriched stable isotopes are very expensive. Therefore it is advisable to use such raw materials more than once. In the last ten years, The authors have used stable isotopes extensively for making of targets. Zinc-67 and zinc-68, cadmium-111 and cadmium-112, nickel-58, silver-109, thallium-203 have been employed for the production of gallium-67, indium-111, cobalt-57, cadmium-109 and thallium-201, respectively. The technique for the recovery of enriched stable isotopes has been developed. In this report the schemes of the recovering processes are presented.

  12. The Nonactinide Isotope and Sealed Sources Management Group

    SciTech Connect (OSTI)

    Low, J. L.; Polansky, G. F.; Parks, D. L.

    2002-02-27T23:59:59.000Z

    The Nonactinide Isotope and Sealed Sources Management Group (NISSMG) is sponsored by the Department of Energy (DOE) Office of Environmental Management and managed by Albuquerque Operations Office (DOE/AL) to serve as a complex-wide resource for the management of DOE-owned Nonactinide Isotope and Sealed Source (NISS) materials. NISS materials are defined as including: any isotope in sealed sources or standards; and isotopes, regardless of form, with atomic number less than 90. The NISSMG assists DOE sites with the storage, reuse, disposition, transportation, and processing of these materials. The NISSMG has focused its efforts to date at DOE closure sites due to the immediacy of their problems. Recently, these efforts were broadened to include closure facilities at non-closure sites. Eventually, the NISSMG plans to make its resources available to all DOE sites. This paper documents the lessons learned in managing NISS materials at DOE sites to date.

  13. Advanced Aqueous Separation Systems for Actinide Partitioning

    SciTech Connect (OSTI)

    Nash, Kenneth L.; Clark, Sue; Meier, G Patrick; Alexandratos, Spiro; Paine, Robert; Hancock, Robert; Ensor, Dale

    2012-03-21T23:59:59.000Z

    One of the most challenging aspects of advanced processing of spent nuclear fuel is the need to isolate transuranium elements from fission product lanthanides. This project expanded the scope of earlier investigations of americium (Am) partitioning from the lanthanides with the synthesis of new separations materials and a centralized focus on radiochemical characterization of the separation systems that could be developed based on these new materials. The primary objective of this program was to explore alternative materials for actinide separations and to link the design of new reagents for actinide separations to characterizations based on actinide chemistry. In the predominant trivalent oxidation state, the chemistry of lanthanides overlaps substantially with that of the trivalent actinides and their mutual separation is quite challenging.

  14. Gas separation using ultrasound and light absorption

    DOE Patents [OSTI]

    Sinha, Dipen N. (Los Alamos, NM)

    2012-07-31T23:59:59.000Z

    An apparatus and method for separating a chosen gas from a mixture of gases having no moving parts and utilizing no chemical processing is described. The separation of particulates from fluid carriers thereof has been observed using ultrasound. In a similar manner, molecular species may be separated from carrier species. It is also known that light-induced drift may separate light-absorbing species from carrier species. Therefore, the combination of temporally pulsed absorption of light with ultrasonic concentration is expected to significantly increase the efficiency of separation by ultrasonic concentration alone. Additionally, breaking the spatial symmetry of a cylindrical acoustic concentrator decreases the spatial distribution of the concentrated particles, and increases the concentration efficiency.

  15. Separative power of an optimised concurrent gas centrifuge

    E-Print Network [OSTI]

    Bogovalov, S V

    2015-01-01T23:59:59.000Z

    The problem of separation of uranium isotopes in a concurrent gas centrifuge is solved analytically. Separative power of the optimized concurrent gas centrifuges equals to $\\delta U=12.7(V/700~{\\rm m/s})^2 (300 ~{\\rm K}/T)L, ~{\\rm kg ~SWU/yr}$, where $L$ and $V$ are the length and linear velocity of the rotor of the gas centrifuge, $T$ is the temperature. This formula well agrees with an empirical separative power of counter current gas centrifuges. The optimal value of the separative power is not unique on the plane $(p_w,v_z)$, where $p_w$ is pressure at the wall of the rotor and $v_z$ is axial velocity of the gas. This value is constant on a line defined by the equation $p_wv_z=constant$. Equations defining the mass flux and the electric power necessary to support the rotation of the gas centrifuge are obtained.

  16. Novel Isotope Effects and Organic Reaction Mechanisms

    E-Print Network [OSTI]

    Kelly, Kelmara K.

    2010-07-14T23:59:59.000Z

    to account for the observed isotope effects. In the dimerization of cyclopentadiene, novel "dynamic" isotope effects are observed on the 13C distribution in the product, and a method for the prediction of these isotope effects is developed here...

  17. Isotope and Nuclear Chemistry Division annual report FY 1986, October 1985-September 1986

    SciTech Connect (OSTI)

    Heiken, J.H. (ed.)

    1987-06-01T23:59:59.000Z

    This report describes progress in the major research and development programs carried out in FY 1986 by the Isotope and Nuclear Chemistry Division. The report includes articles on radiochemical diagnostics and weapons tests; weapons radiochemical diagnostics research and development; other unclassified weapons research; stable and radioactive isotope production and separation; chemical biology and nuclear medicine; element and isotope transport and fixation; actinide and transition metal chemistry; structural chemistry, spectroscopy, and applications; nuclear structure and reactions; irradiation facilities; advanced concepts and technology; and atmospheric chemistry.

  18. Performance improvement of Gas-Liquid Cylindrical Cyclone separator using different design for tangential inlet

    E-Print Network [OSTI]

    Barbuceanu, Nicolae

    2001-01-01T23:59:59.000Z

    separators often rely on centrifugal forces to enhance the separation process and are therefore highly dependent on inlet geometry. This paper investigates expanding the operational envelope of a compact Gas-Liquid Cylindrical Cyclone separator through...

  19. Four-port gas separation membrane module assembly

    DOE Patents [OSTI]

    Wynn, Nicholas P. (Redwood City, CA); Fulton, Donald A. (Fairfield, CA); Lokhandwala, Kaaeid A. (Fremont, CA); Kaschemekat, Jurgen (Campbell, CA)

    2010-07-20T23:59:59.000Z

    A gas-separation membrane assembly, and a gas-separation process using the assembly. The assembly incorporates multiple gas-separation membranes in an array within a single vessel or housing, and is equipped with two permeate ports, enabling permeate gas to be withdrawn from both ends of the membrane module permeate pipes.

  20. Membrane separation advances in FE hydrogen program

    SciTech Connect (OSTI)

    NONE

    2007-12-31T23:59:59.000Z

    Since its inception in Fiscal Year 2003 the US Office of Fossil Energy (FE) Hydrogen from Coal Program has sponsored more than 60 projects and made advances in the science of separating out pure hydrogen from syngas produced through coal gasification. The Program is focusing on advanced hydrogen separation technologies, which include membranes, and combining the WGS reaction and hydrogen separation in a single operation known as process intensification. The article explains the technologies and describes some key FE membrane projects. More details are available from http://www.fossil.energy.gov. 1 fig.

  1. ARM - Measurement - Isotope ratio

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625govInstrumentstdmadap Documentation TDMADAP : XDC documentationBarrow,ice particleSizegovMeasurementsIsotope ratio

  2. Stable Isotope Fractionations in Biogeochemical Reactive Transport

    E-Print Network [OSTI]

    Druhan, Jennifer Lea

    2012-01-01T23:59:59.000Z

    characteristic of stable isotope enrichment. The values of !isotope ratios of sulfur in these sulfate samples demonstrated a clear enrichmentisotope ( 34 S) (Canfield, 2001). The characteristic enrichment

  3. Strategic Isotope Production | ornl.gov

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Strategic Isotope Production SHARE Strategic Isotope Production Typical capsules used in the transport of 252Cf source material inside heavily shielded shipping casks. ORNL's...

  4. Isotopic Trends in Production of Superheavies

    SciTech Connect (OSTI)

    Antonenko, N.V. [Institut fuer Theoretische Physik der Justus-Liebig-Universitaet, D-35392 Giessen (Germany); Joint Institute for Nuclear Research, 141980 Dubna (Russian Federation); Adamian, G.G.; Zubov, A.S. [Joint Institute for Nuclear Research, 141980 Dubna (Russian Federation); Scheid, W. [Institut fuer Theoretische Physik der Justus-Liebig-Universitaet, D-35392 Giessen (Germany)

    2005-11-21T23:59:59.000Z

    The isotopic trends are discussed for cold and hot fusion reactions leading to superheavies. The possibilities of production of new isotopes in incomplete fusion reactions are treated.

  5. T. Larsson, S. Skogestad, C.C. Yu Control of reactor, separator with recycle. Control of reactor, separator with recycle.

    E-Print Network [OSTI]

    Skogestad, Sigurd

    T. Larsson, S. Skogestad, C.C. Yu Control of reactor, separator with recycle. Control of reactor, separator with recycle. Liquid phase system gas phase systems methanol synthesis loop T. Larsson S, separator with recycle. Motivation, background and related work ¯ Common feature of many chemical processes

  6. Separators for electrochemical cells

    DOE Patents [OSTI]

    Carlson, Steven Allen; Anakor, Ifenna Kingsley

    2014-11-11T23:59:59.000Z

    Provided are separators for use in an electrochemical cell comprising (a) an inorganic oxide and (b) an organic polymer, wherein the inorganic oxide comprises organic substituents. Preferably, the inorganic oxide comprises an hydrated aluminum oxide of the formula Al.sub.2O.sub.3.xH.sub.2O, wherein x is less than 1.0, and wherein the hydrated aluminum oxide comprises organic substituents, preferably comprising a reaction product of a multifunctional monomer and/or organic carbonate with an aluminum oxide, such as pseudo-boehmite and an aluminum oxide. Also provided are electrochemical cells comprising such separators.

  7. Isotope Research 229 Th production

    E-Print Network [OSTI]

    Isotope Research ­ 229 Th production We recently completed an ARRA-funded project of this type on 229 Th production reactions [Str11]. This long-lived isotope is important as a precursor to 225 Ac of accelerator production of 229 Th via the 230 Th(p,2n)229 Pa reaction. The 229 Pa decays primarily by electron

  8. Development of FCC catalyst magnetic separation

    SciTech Connect (OSTI)

    Goolsby, T.L.; Moore, H.F. [Ashland Petroleum Co., KY (United States)

    1997-01-01T23:59:59.000Z

    Magnetic separation has been historically active in several different industries, yet has not been utilized in petroleum refining until recently. Development of economical permanent magnets with high magnetic strength has led to a new process known as MagnaCat{reg_sign}. The MagnaCat{reg_sign}. Process separates less active (high metals) particles catalyst from equilibrium Fluid Catalytic Cracking (FCC) catalyst, producing a higher activity/lower metals catalyst for recycle. Pilot FCC studies showed lower hydrogen, dry gas, and coke make with higher wet gas and octane from catalyst separated by MagnaCat{reg_sign}. With the use of a MagnaCat{reg_sign} Process unit, a refiner would produce an economic advantage of $0.20 to $0.40/Barrel of FCC charge and enhance unit operability.

  9. Molten salt electrolyte separator

    DOE Patents [OSTI]

    Kaun, T.D.

    1996-07-09T23:59:59.000Z

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

  10. Polymide gas separation membranes

    DOE Patents [OSTI]

    Ding, Yong; Bikson, Benjamin; Nelson, Joyce Katz

    2004-09-14T23:59:59.000Z

    Soluble polyamic acid salt (PAAS) precursors comprised of tertiary and quaternary amines, ammonium cations, sulfonium cations, or phosphonium cations, are prepared and fabricated into membranes that are subsequently imidized and converted into rigid-rod polyimide articles, such as membranes with desirable gas separation properties. A method of enhancing solubility of PAAS polymers in alcohols is also disclosed.

  11. NEAMS safeguards and separations

    SciTech Connect (OSTI)

    Sadasivan, Pratap [Los Alamos National Laboratory; De Paoli, David W [ORNL

    2011-01-25T23:59:59.000Z

    This presentation provides a program management update on the Safeguards and Separations Integrated Performance and Safety Code (IPSC) program in the DOE Nuclear Energy Advanced Modeling and Simulation (NEAMS). It provides an overview of FY11 work packages at multiple DOE Labs and includes material on challenge problem definitions for the IPSC effort.

  12. Thorium isotopes in the western Mediterranean Sea: an insight into the marine particle dynamics

    E-Print Network [OSTI]

    Coppola, Laurent

    Thorium isotopes in the western Mediterranean Sea: an insight into the marine particle dynamics M rights reserved. Keywords: thorium; isotopes; sea water; particles; sedimentation; Mediterranean Sea 1 physical, chemical and biological processes and sometimes non-steady-state condi- tions [1^4]. Thorium

  13. Experimental determination of equilibrium nickel isotope fractionation between metal and silicate from 500 C

    E-Print Network [OSTI]

    Manning, Craig

    Experimental determination of equilibrium nickel isotope fractionation between metal and silicate.04& between equilibrated bulk silicate Earth and chondrites, indicating that Ni isotopes are not likely- lation process involving a well-mixed silicate reservoir. Ã? 2012 Elsevier Ltd. All rights reserved. 1

  14. Helium Isotopic Textures in Earth's Upper Mantle David W. Graham a

    E-Print Network [OSTI]

    Graham, David W.

    Helium Isotopic Textures in Earth's Upper Mantle David W. Graham a , Barry B. Hanan b , Christophe of variability represent a description of helium isotopic texture. We utilize four complementary methods (~100 km) mantle flow, and by sampling during the partial melting process (~30 km). Keywords: helium

  15. A Non-Aqueous Reduction Process for Purifying 153Gd Produced in Natural Europium Targets

    SciTech Connect (OSTI)

    Johnsen, Amanda M.; Soderquist, Chuck Z.; McNamara, Bruce K.; Fisher, Darrell R.

    2013-08-01T23:59:59.000Z

    Gadolinium-153 is a low-energy gamma-emitter used in nuclear medicine imaging quality assurance. Produced in nuclear reactors using natural Eu2O3 targets, 153Gd is radiochemically separated from europium isotopes by europium reduction. However, conventional aqueous europium reduction produces hydrogen gas, a flammability hazard in radiological hot cells. We altered the traditional reduction method, using methanol as the process solvent to nearly eliminate hydrogen gas production. This new, non-aqueous reduction process demonstrates greater than 98% europium removal and gadolinium yields of 90%.

  16. Two stroke engine exhaust emissions separator

    DOE Patents [OSTI]

    Turner, Terry D. (Ammon, ID); Wilding, Bruce M. (Idaho Falls, ID); McKellar, Michael G. (Idaho Falls, ID); Raterman, Kevin T. (Idaho Falls, ID)

    2002-01-01T23:59:59.000Z

    A separator for substantially resolving at least one component of a process stream, such as from the exhaust of an internal combustion engine. The separator includes a body defining a chamber therein. A nozzle housing is located proximate the chamber. An exhaust inlet is in communication with the nozzle housing and the chamber. A nozzle assembly is positioned in the nozzle housing and includes a nozzle moveable within and relative to the nozzle housing. The nozzle includes at least one passage formed therethrough such that a process stream entering the exhaust inlet connection passes through the passage formed in the nozzle, which imparts a substantially rotational flow to the process stream as it enters the chamber. A positioning member is configured to position the nozzle relative to the nozzle housing in response to changes in process stream pressure to adjust flowrate of said process stream entering into the chamber.

  17. Two stroke engine exhaust emissions separator

    DOE Patents [OSTI]

    Turner, Terry D. (Ammon, ID); Wilding, Bruce M. (Idaho Falls, ID); McKellar, Michael G. (Idaho Falls, ID); Raterman, Kevin T. (Idaho Falls, ID)

    2003-04-22T23:59:59.000Z

    A separator for substantially resolving at least one component of a process stream, such as from the exhaust of an internal combustion engine. The separator includes a body defining a chamber therein. A nozzle housing is located proximate the chamber. An exhaust inlet is in communication with the nozzle housing and the chamber. A nozzle assembly is positioned in the nozzle housing and includes a nozzle moveable within and relative to the nozzle housing. The nozzle includes at least one passage formed therethrough such that a process stream entering the exhaust inlet connection passes through the passage formed in the nozzle and imparts a substantially rotational flow to the process stream as it enters the chamber. A positioning member is configured to position the nozzle relative to the nozzle housing in response to changes in process stream pressure thereby adjusting flowrate of said process stream entering into the chamber.

  18. Compact hydrogen/helium isotope mass spectrometer

    DOE Patents [OSTI]

    Funsten, Herbert O. (Los Alamos, NM); McComas, David J. (Los Alamos, NM); Scime, Earl E. (Morgantown, WV)

    1996-01-01T23:59:59.000Z

    The compact hydrogen and helium isotope mass spectrometer of the present invention combines low mass-resolution ion mass spectrometry and beam-foil interaction technology to unambiguously detect and quantify deuterium (D), tritium (T), hydrogen molecule (H.sub.2, HD, D.sub.2, HT, DT, and T.sub.2), .sup.3 He, and .sup.4 He concentrations and concentration variations. The spectrometer provides real-time, high sensitivity, and high accuracy measurements. Currently, no fieldable D or molecular speciation detectors exist. Furthermore, the present spectrometer has a significant advantage over traditional T detectors: no confusion of the measurements by other beta-emitters, and complete separation of atomic and molecular species of equivalent atomic mass (e.g., HD and .sup.3 He).

  19. Membrane augmented distillation to separate solvents from water

    DOE Patents [OSTI]

    Huang, Yu; Baker, Richard W.; Daniels, Rami; Aldajani, Tiem; Ly, Jennifer H.; Alvarez, Franklin R.; Vane, Leland M.

    2012-09-11T23:59:59.000Z

    Processes for removing water from organic solvents, such as ethanol. The processes include distillation to form a rectified overhead vapor, compression of the rectified vapor, and treatment of the compressed vapor by two sequential membrane separation steps.

  20. doi:10.1016/j.gca.2003.12.008 Nd-, O-, and H-isotopic evidence for complex, closed-system fluid evolution of the

    E-Print Network [OSTI]

    Siebel, Wolfgang

    , Eberhard-Karls-Universita¨t, Wilhelmstra e 56, D-72074 Tu¨bingen, Germany 2 Institut de Mine´ralogie et Ge, clinopyroxene, and olivine separates ( 5.2 to 5.7 relative to VSMOW) and neodymium isotope compositions ( Nd. In contrast to the homogeneous oxygen and neodymium isotopic data, D values for hand-picked amphibole

  1. Steam separator latch assembly

    DOE Patents [OSTI]

    Challberg, R.C.; Kobsa, I.R.

    1994-02-01T23:59:59.000Z

    A latch assembly removably joins a steam separator assembly to a support flange disposed at a top end of a tubular shroud in a nuclear reactor pressure vessel. The assembly includes an annular head having a central portion for supporting the steam separator assembly thereon, and an annular head flange extending around a perimeter thereof for supporting the head to the support flange. A plurality of latches are circumferentially spaced apart around the head flange with each latch having a top end, a latch hook at a bottom end thereof, and a pivot support disposed at an intermediate portion therebetween and pivotally joined to the head flange. The latches are pivoted about the pivot supports for selectively engaging and disengaging the latch hooks with the support flange for fixedly joining the head to the shroud or for allowing removal thereof. 12 figures.

  2. Steam separator latch assembly

    DOE Patents [OSTI]

    Challberg, Roy C. (Livermore, CA); Kobsa, Irvin R. (San Jose, CA)

    1994-01-01T23:59:59.000Z

    A latch assembly removably joins a steam separator assembly to a support flange disposed at a top end of a tubular shroud in a nuclear reactor pressure vessel. The assembly includes an annular head having a central portion for supporting the steam separator assembly thereon, and an annular head flange extending around a perimeter thereof for supporting the head to the support flange. A plurality of latches are circumferentially spaced apart around the head flange with each latch having a top end, a latch hook at a bottom end thereof, and a pivot support disposed at an intermediate portion therebetween and pivotally joined to the head flange. The latches are pivoted about the pivot supports for selectively engaging and disengaging the latch hooks with the support flange for fixedly joining the head to the shroud or for allowing removal thereof.

  3. Membrane separation of hydrocarbons

    DOE Patents [OSTI]

    Funk, Edward W. (Highland Park, IL); Kulkarni, Sudhir S. (Hoffman Estates, IL); Chang, Y. Alice (Des Plaines, IL)

    1986-01-01T23:59:59.000Z

    Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture over a polymeric membrane which comprises a polymer capable of maintaining its integrity in the presence of hydrocarbon compounds at temperature ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psi. The membranes which possess pore sizes ranging from about 10 to about 500 Angstroms are cast from a solvent solution and recovered.

  4. Compelling Research Opportunities using Isotopes

    SciTech Connect (OSTI)

    None

    2009-04-23T23:59:59.000Z

    Isotopes are vital to the science and technology base of the US economy. Isotopes, both stable and radioactive, are essential tools in the growing science, technology, engineering, and health enterprises of the 21st century. The scientific discoveries and associated advances made as a result of the availability of isotopes today span widely from medicine to biology, physics, chemistry, and a broad range of applications in environmental and material sciences. Isotope issues have become crucial aspects of homeland security. Isotopes are utilized in new resource development, in energy from bio-fuels, petrochemical and nuclear fuels, in drug discovery, health care therapies and diagnostics, in nutrition, in agriculture, and in many other areas. The development and production of isotope products unavailable or difficult to get commercially have been most recently the responsibility of the Department of Energy's Nuclear Energy program. The President's FY09 Budget request proposed the transfer of the Isotope Production program to the Department of Energy's Office of Science in Nuclear Physics and to rename it the National Isotope Production and Application program (NIPA). The transfer has now taken place with the signing of the 2009 appropriations bill. In preparation for this, the Nuclear Science Advisory Committee (NSAC) was requested to establish a standing subcommittee, the NSAC Isotope Subcommittee (NSACI), to advise the DOE Office of Nuclear Physics. The request came in the form of two charges: one, on setting research priorities in the short term for the most compelling opportunities from the vast array of disciplines that develop and use isotopes and two, on making a long term strategic plan for the NIPA program. This is the final report to address charge 1. NSACI membership is comprised of experts from the diverse research communities, industry, production, and homeland security. NSACI discussed research opportunities divided into three areas: (1) medicine, pharmaceuticals, and biology, (2) physical sciences and engineering, and (3) national security and other applications. In each area, compelling research opportunities were considered and the subcommittee as a whole determined the final priorities for research opportunities as the foundations for the recommendations. While it was challenging to prioritize across disciplines, our order of recommendations reflect the compelling research prioritization along with consideration of time urgency for action as well as various geopolitical market issues. Common observations to all areas of research include the needs for domestic availability of crucial stable and radioactive isotopes and the education of the skilled workforce that will develop new advances using isotopes in the future. The six recommendations of NSACI reflect these concerns and the compelling research opportunities for potential new discoveries. The science case for each of the recommendations is elaborated in the respective chapters.

  5. The use of carbohydrazide for plutonium concentration stripping in separator with inert packing

    SciTech Connect (OSTI)

    Dvoeglazov, K.; Volk, V.; Zverev, D.; Veselov, S. [JSC - A.A. Bochvar VNIINM -, Moscow (Russian Federation); Krivitskiy, Y.; Alekseenko, S. [FSUE - Mining and Chemical Plant -, Zheleznogorsk (Russian Federation); Alekseenko, V. [FSUE - Federal Centre for Nuclear and Radiation Safety -, Moscow (Russian Federation)

    2013-07-01T23:59:59.000Z

    For the purpose of removing plutonium from uranium- plutonium extract it is proposed to employ concentration stripping process with the use of separator and a new reducing reagent: Carbohydrazide CO(N{sub 2}H{sub 3}){sub 2}. Using plutonium stripping from solution simulating the composition of extract of spent nuclear fuel from VVER-1000 reactor (without ?-emitting isotopes), with O: A ratio of = 28, a product solution was obtained containing 17.8 g/l of plutonium, 29.2 g/l of uranium and more than 1 g/l of technetium. The experiment on real spent fuel from VVER-1000 with burn-up of more than 50 GW*d/t of uranium after 17 year exposure, performed in the shielded box of FSUE 'MCP', confirmed the effectiveness and feasibility of the proposed process. Through concentration stripping (O:A = 20), a plutonium product solution was obtained with a part of uranium with the following composition: [U] = 150 g/l; [Pu] = 23,5 g/l; [Np] = 1,7 g/l, [Tc] = 1.5 g/l; gamma exposure rate - 0,022 mR/s*l. Direct extraction of plutonium in this operation was 95.3%, the rest of plutonium is refluxing to the preceding stage of the extraction cycle. A process flow diagram with organization of plutonium recycling is proposed, allowing for its complete removal into a single stream. Carbohydrazide is an effective reducing agent of plutonium (IV), ensuring the stability of uranium-plutonium separation process. (authors)

  6. Separations and safeguards model integration.

    SciTech Connect (OSTI)

    Cipiti, Benjamin B.; Zinaman, Owen

    2010-09-01T23:59:59.000Z

    Research and development of advanced reprocessing plant designs can greatly benefit from the development of a reprocessing plant model capable of transient solvent extraction chemistry. This type of model can be used to optimize the operations of a plant as well as the designs for safeguards, security, and safety. Previous work has integrated a transient solvent extraction simulation module, based on the Solvent Extraction Process Having Interaction Solutes (SEPHIS) code developed at Oak Ridge National Laboratory, with the Separations and Safeguards Performance Model (SSPM) developed at Sandia National Laboratory, as a first step toward creating a more versatile design and evaluation tool. The goal of this work was to strengthen the integration by linking more variables between the two codes. The results from this integrated model show expected operational performance through plant transients. Additionally, ORIGEN source term files were integrated into the SSPM to provide concentrations, radioactivity, neutron emission rate, and thermal power data for various spent fuels. This data was used to generate measurement blocks that can determine the radioactivity, neutron emission rate, or thermal power of any stream or vessel in the plant model. This work examined how the code could be expanded to integrate other separation steps and benchmark the results to other data. Recommendations for future work will be presented.

  7. Hydrogen recovery process

    DOE Patents [OSTI]

    Baker, Richard W. (Palo Alto, CA); Lokhandwala, Kaaeid A. (Union City, CA); He, Zhenjie (Fremont, CA); Pinnau, Ingo (Palo Alto, CA)

    2000-01-01T23:59:59.000Z

    A treatment process for a hydrogen-containing off-gas stream from a refinery, petrochemical plant or the like. The process includes three separation steps: condensation, membrane separation and hydrocarbon fraction separation. The membrane separation step is characterized in that it is carried out under conditions at which the membrane exhibits a selectivity in favor of methane over hydrogen of at least about 2.5.

  8. Stable isotopes of authigenic minerals in variably-saturated fractured tuff

    SciTech Connect (OSTI)

    Weber, D.S.; Evans, D.D.

    1988-11-01T23:59:59.000Z

    Identifying stable isotope variation and mineralogical changes in fractured rock may help establish the history of climatic and geomorphological processes that might affect the isolation properties of a waste repository site. This study examines the use of the stable isotope ratios of oxygen ({sup 18}O/{sup 16}O) and carbon ({sup 13}C/{sup 12}C) in authigenic minerals as hydrogeochemical tools tracing low-temperature rock-water interaction in variably-saturated fractured stuff. Isotopic compositions of fracture-filling and rock matrix minerals in the Apache Leap tuff, near Superior, Arizona were concordant with geothermal temperatures and in equilibrium with water isotopically similar to present-day meteoric water and groundwater. Oxygen and carbon isotope ratios of fracture-filling, in unsaturated fractured tuff, displayed an isotopic gradient believed to result from near-surface isotopic enrichment due to evaporation rather than the effects of rock-water interaction. Oxygen isotope ratios of rock matrix opal samples exhibited an isotopic gradient believed to result from, leaching and reprecipitation of silica at depth. Methods and results can be used to further define primary flowpaths and the movement of water in variably-saturated fractured rock. 71 refs., 23 figs., 3 tabs.

  9. Physics with isotopically controlled semiconductors

    SciTech Connect (OSTI)

    Haller, E. E., E-mail: eehaller@lbl.gov [University of California at Berkeley, Department of Materials Science and Engineering (United States)

    2010-07-15T23:59:59.000Z

    This paper is based on a tutorial presentation at the International Conference on Defects in Semiconductors (ICDS-25) held in Saint Petersburg, Russia in July 2009. The tutorial focused on a review of recent research involving isotopically controlled semiconductors. Studies with isotopically enriched semiconductor structures experienced a dramatic expansion at the end of the Cold War when significant quantities of enriched isotopes of elements forming semiconductors became available for worldwide collaborations. Isotopes of an element differ in nuclear mass, may have different nuclear spins and undergo different nuclear reactions. Among the latter, the capture of thermal neutrons which can lead to neutron transmutation doping, is the most prominent effect for semiconductors. Experimental and theoretical research exploiting the differences in all the properties has been conducted and will be illustrated with selected examples.

  10. Isotope Biogeochemistry of Diagenesis caused by a Black

    E-Print Network [OSTI]

    Isotope Biogeochemistry of Diagenesis caused by a Black Shale-fueled Deep Marine Biosphere (ODP Leg Forschungsgemeinschaft and Max Planck Society #12;Black shales and Diagenesis: Processes and Proxies - Authigenic sulfur the coasts of Surinam and French Guyana #12;µ Black shales in Leg 207 sediments and pore water response depth

  11. isotopic ratio | EMSL

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Molecular Science Computing Facility: Quiet Wing Science Theme: Biosystem Dynamics & Design Terrestrial & Subsurface Ecosystems Energy Materials & Processes Atmospheric...

  12. Isotopic generator for bismuth-212 and lead-212 from radium

    DOE Patents [OSTI]

    Atcher, Robert W. (Kensington, MD); Friedman, Arnold M. (Park Forest, IL); Hines, John (Glen Ellyn, IL)

    1987-01-01T23:59:59.000Z

    A method and apparatus for providing radionuclides of bismuth-212 and lead-212. Thorium-228 and carrier solution starting material is input to a radiologically contained portion of an isotopic generator system, and radium-224 is separated from thorium-228 which is retained by a strongly basic anion exchange column. The separated radium-224 is transferred to an accessible, strongly acidic cationic exchange column. The cationic column retains the radium-224, and natural radioactive decay generates bismuth-212 and lead-212. The cationic exchange column can also be separated from the contained portion of the system and utilized without the extraordinary safety measures necessary in the contained portion. Furthermore, the cationic exchange column provides over a relatively long time period the short lived lead-212 and bismuth-212 radionuclides which are useful for a variety of medical therapies.

  13. Component separation with flexible models. Application to the separation of astrophysical emissions

    E-Print Network [OSTI]

    Jean-Francois Cardoso; Maude Martin; Jacques Delabrouille; Marc Betoule; Guillaume Patanchon

    2008-03-12T23:59:59.000Z

    This paper offers a new point of view on component separation, based on a model of additive components which enjoys a much greater flexibility than more traditional linear component models. This flexibility is needed to process the complex full-sky observations of the CMB expected from the Planck space mission, for which it was developed, but it may also be useful in any context where accurate component separation is needed.

  14. Isotope production facility produces cancer-fighting actinium

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Cancer therapy gets a boost from new isotope Isotope production facility produces cancer-fighting actinium A new medical isotope project shows promise for rapidly producing major...

  15. Analysis of the ecology of Anchialine Caves using carbon and nitrogen stable isotopes

    E-Print Network [OSTI]

    Pohlman, John William

    1995-01-01T23:59:59.000Z

    Carbon and nitrogen stable isotopes were used to investigate the biogeochemical and ecological processes that govern anchialine cave ecosystems in the Yucatan Peninsula, Quintana Roo, Mexico. Anchialine caves are subterranean passages...

  16. Soil water utilization by herbaceous species of the southern Great Plains: evidence from isotopically labeled water

    E-Print Network [OSTI]

    Yoder, Carolyn Kay

    1993-01-01T23:59:59.000Z

    Understanding spatial and temporal patterns of soil water utilization by plants has broad implications for physiological, ecological, and hydrological processes. Water labeled with the stable isotopes deuterium ('H) or oxygen-18 ("'O) was injected...

  17. LITHIUM ISOTOPIC COMPOSITION OF CHONDRITIC METEORITES. W. F. McDonough1 , P. B. Tomascak1

    E-Print Network [OSTI]

    Mcdonough, William F.

    LITHIUM ISOTOPIC COMPOSITION OF CHONDRITIC METEORITES. W. F. McDonough1 , F- Z. Teng1 , P. B processes involving aqueous fluids, given the potential solubility of lithium [1]. In this respect, Li

  18. ISOTOPIC COMPOSITION OF LIGHT NUCLEI IN COSMIC RAYS: RESULTS FROM AMS-01

    E-Print Network [OSTI]

    Becker, R.

    The variety of isotopes in cosmic rays allows us to study different aspects of the processes that cosmic rays undergo between the time they are produced and the time of their arrival in the heliosphere. In this paper, we ...

  19. Isotope effects in the CO dimer: Millimeter wave spectrum and rovibrational calculations of ,,12

    E-Print Network [OSTI]

    . M. Vissers Department of Chemistry, The Ohio State University, Columbus, Ohio 43210 A. van der. The isotopic dependence of the A+ /A- energy splitting, the intermolecular separation R, and the energy in understanding the previously mysteri- ous spectra of the carbon monoxide dimer as well as its energy level

  20. Isotopically Enriched Films and Nanostructures by Ultrafast Pulsed Laser Deposition

    SciTech Connect (OSTI)

    Peter Pronko

    2004-12-13T23:59:59.000Z

    This project involved a systematic study to apply newly discovered isotopic enrichment effects in laser ablation plumes to the fabrication of isotopically engineered thin films, superlattices, and nanostructures. The approach to this program involved using ultrafast lasers as a method for generating ablated plasmas that have preferentially structured isotopic content in the body of the ablation plasma plumes. In examining these results we have attempted to interpret the observations in terms of a plasma centrifuge process that is driven by the internal electro-magnetic fields of the plasma itself. The research plan involved studying the following phenomena in regard to the ablation plume and the isotopic mass distribution within it: (1) Test basic equations of steady state centrifugal motion in the ablation plasma. (2) Investigate angular distribution of ions in the ablation plasmas. (3) Examine interactions of plasma ions with self-generated magnetic fields. (3) Investigate ion to neutral ratios in the ablation plasmas. (5) Test concepts of plasma pumping. (6) Fabricate isotopically enriched nanostructures.

  1. Oxygen isotopic ratios in intermediate-mass red giants

    E-Print Network [OSTI]

    Lebzelter, Thomas; Hinkle, Kenneth; Nowotny, Walter; Aringer, Bernhard

    2015-01-01T23:59:59.000Z

    Context. The abundances of the three main isotopes of oxygen are altered in the course of the CNO-cycle. When the first dredge-up mixes the burning products to the surface, the nucleosynthesis processes can be probed by measuring oxygen isotopic ratios. Aims. By measuring 16O/17O and 16O/18O in red giants of known mass we compare the isotope ratios with predictions from stellar and galactic evolution modelling. Methods. Oxygen isotopic ratios were derived from the K-band spectra of six red giants. The sample red giants are open cluster members with known masses of between 1.8 and 4.5 Msun . The abundance determination employs synthetic spectra calculated with the COMARCS code. The effect of uncertainties in the nuclear reaction rates, the mixing length, and of a change in the initial abundance of the oxygen isotopes was determined by a set of nucleosynthesis and mixing models using the FUNS code. Results. The observed 16O/17O ratios are in good agreement with the model results, even if the measured values do ...

  2. The use of carbon stable isotope ratios in drugs characterization

    SciTech Connect (OSTI)

    Magdas, D. A., E-mail: gabriela.cristea@itim-cj.ro; Cristea, G., E-mail: gabriela.cristea@itim-cj.ro; Bot, A., E-mail: gabriela.cristea@itim-cj.ro; Mirel, V., E-mail: gabriela.cristea@itim-cj.ro [National Institute for Research and Development of Isotopic and Molecular Technologies, 65-103 Donath Str., 400293 Cluj-Napoca (Romania)

    2013-11-13T23:59:59.000Z

    Isotopic Ratio Mass Spectrometry (IRMS) is an effective toll to be used for drug product authentication. The isotopic composition could be used to assist in the differentiation between batches of drugs and assist in the identification of counterfeit materials on the market. Only two factors affect the isotopic ratios in pharmaceutical components: the isotopic composition of the raw materials and the synthetic processes performed upon them. Counterfeiting of pharmaceutical drugs threatens consumer confidence in drug products companies' economical well-being. In this preliminary study, the analyzed samples consist in two types of commercially available analgesics, which were purchases from Romanian pharmacies. Differences in ?{sup 13}C between batches from ?29.7 to ?31.6% were observed, demonstrating that this method can be used to differentiate among individual drug batches and subsequently identify counterfeits on the market. On the other hand, carbon isotopic ratios differences among producers were recorded, the variations being between ?31.3 to ?34.9% for the same type of analgesic, but from different manufactures.

  3. ZIRCONIUM—HAFNIUM ISOTOPE EVIDENCE FROM METEORITES FOR THE DECOUPLED SYNTHESIS OF LIGHT AND HEAVY NEUTRON-RICH NUCLEI

    SciTech Connect (OSTI)

    Akram, W.; Schönbächler, M. [School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL (United Kingdom); Sprung, P. [Institut für Planetologie, Universität Münster, Wilhelm-Klemm-Strasse 10, D-48149 Münster (Germany); Vogel, N. [Institute for Geochemistry and Petrology, ETH, Clausiusstrasse 25, 8092 Zürich (Switzerland)

    2013-11-10T23:59:59.000Z

    Recent work based on analyses of meteorite and terrestrial whole-rock samples showed that the r- and s- process isotopes of Hf were homogeneously distributed throughout the inner solar system. We report new Hf isotope data for Calcium-Aluminum-rich inclusions (CAIs) of the CV3 carbonaceous chondrite Allende, and novel high-precision Zr isotope data for these CAIs and three carbonaceous chondrites (CM, CO, CK). Our Zr data reveal enrichments in the neutron-rich isotope {sup 96}Zr (?1? in {sup 96}Zr/{sup 90}Zr) for bulk chondrites and CAIs (?2?). Potential isotope effects due to incomplete sample dissolution, galactic and cosmic ray spallation, and the nuclear field shift are assessed and excluded, leading to the conclusion that the {sup 96}Zr isotope variations are of nucleosynthetic origin. The {sup 96}Zr enrichments are coupled with {sup 50}Ti excesses suggesting that both nuclides were produced in the same astrophysical environment. The same CAIs also exhibit deficits in r-process Hf isotopes, which provides strong evidence for a decoupling between the nucleosynthetic processes that produce the light (A ? 130) and heavy (A > 130) neutron-rich isotopes. We propose that the light neutron-capture isotopes largely formed in Type II supernovae (SNeII) with higher mass progenitors than the supernovae that produced the heavy r-process isotopes. In the context of our model, the light isotopes (e.g. {sup 96}Zr) are predominantly synthesized via charged-particle reactions in a high entropy wind environment, in which Hf isotopes are not produced. Collectively, our data indicates that CAIs sampled an excess of materials produced in a normal mass (12-25 M{sub ?}) SNII.

  4. Physical Separation and Multiphase

    E-Print Network [OSTI]

    Sóbester, András

    - research into CVD and HVOF coatings for subsea choke valve applications. s US Navy - understanding the processes of charge generation in gear contacts as a predictive maintenance tool. s DRA/UoS - corrosion

  5. Charge separation in organic photovoltaic cells

    E-Print Network [OSTI]

    Giazitzidis, Paraskevas; Bisquert, Juan; Vikhrenko, Vyacheslav S

    2014-01-01T23:59:59.000Z

    We consider a simple model for the geminate electron-hole separation process in organic photovoltaicssss cells, in order to illustrate the influence of dimensionality of conducting channels on the efficiency of the process. The Miller-Abrahams expression for the transition rates between nearest neighbor sites was used for simulating random walks of the electron in the Coulomb field of the hole. The non-equilibrium kinetic Monte Carlo simulation results qualitatively confirm the equilibrium estimations, although quantitatively the efficiency of the higher dimensional systems is less pronounced. The lifetime of the electron prior to recombination is approximately equal to the lifetime prior to dissociation. Their values indicate that electrons perform long stochastic walks before they are captured by the collector or recombined. The non-equilibrium free energy considerably differs from the equilibrium one. The efficiency of the separation process decreases with increasing the distance to the collector, and this...

  6. Nickel isotopes in stellar matter

    E-Print Network [OSTI]

    Jameel-Un Nabi

    2014-08-19T23:59:59.000Z

    Isotopes of nickel play a key role during the silicon burning phase up to the presupernova phase of massive stars. Electron capture rates on these nickel isotopes are also important during the phase of core contraction. I present here the microscopic calculation of ground and excited states Gamow-Teller (GT) strength distributions for key nickel isotopes. The calculation is performed within the frame-work of pn-QRPA model. A judicious choice of model parameters, specially of the Gamow-Teller strength parameters and the deformation parameter, resulted in a much improved calculation of GT strength functions. The excited state GT distributions are much different from the corresponding ground-state distributions resulting in a failure of the Brink's hypothesis. The electron capture and positron decay rates on nickel isotopes are also calculated within the framework of pn-QRPA model relevant to the presupernova evolution of massive stars. The electron capture rates on odd-A isotopes of nickel are shown to have dominant contributions from parent excited states during as early as silicon burning phases. Comparison is being made with the large scale shell model calculation. During the silicon burning phases of massive stars the electron capture rates on $^{57,59}$Ni are around an order of magnitude bigger than shell model rates and can bear consequences for core-collapse simulators.

  7. Carbon isotope fractionation in plants. Final technical report, June 1, 1983-May 31, 1986

    SciTech Connect (OSTI)

    O'Leary, M.H.

    1986-09-01T23:59:59.000Z

    Plants fractionate carbon isotopes during photosynthesis in ways which reflect photosynthetic pathway and environment. The object of our work is to develop methods for using this isotope fractionation to give information about how the components of the carbon fixation process (diffusion, carboxylation, etc.) vary with species, environment, and other variables. These studies provide important information regarding environmental control of the efficiency of photosynthesis as well as information regarding changes in photosynthesis which can be expected in coming years as atmospheric carbon dioxide levels increase. To this end, we have developed quantitative models for carbon isotope fractionation which describe this process in terms of rates of diffusion, carboxylation, and other steps. We have developed experimental approaches which focus on the initial events in carbon dioxide fixation and enable us to determine the relative rates of the various individual processes involved. Our approaches are unique in that they provide a view of the carbon isotope fractionation process over a period of a few hours, whereas combustion methods used by previous investigators provide only a long-term view of the carbon isotope fractionation process. We have also developed other methods using stable isotopes which rely on NMR and mass spectral measurements to study plant metabolism. 61 refs., 5 figs., 4 tabs.

  8. Mechanistic studies using kinetic isotope effects

    E-Print Network [OSTI]

    Schulmeier, Brian E.

    1999-01-01T23:59:59.000Z

    Understanding reaction mechanisms is an important aspect of chemistry. A now convenient way to study reaction mechanisms is kinetic isotope effects at natural abundance. This technique circumvents the cumbersome methods of traditional isotope effect...

  9. ENRICHED STABLE ISOTOPE TARGET PREPARATION AT THE OAK RIDGE NATIONAL LABORATORY

    SciTech Connect (OSTI)

    Aaron, W Scott [ORNL] [ORNL; Zevenbergen, Lee [ORNL] [ORNL

    2013-01-01T23:59:59.000Z

    Since the 1960s the Department of Energy (DOE) Isotope Program, through the Isotope Development Group at the Oak Ridge National Laboratory, has been developing and supplying, among other things, enriched stable isotope targets for nuclear research around the world. This group also maintains and distributes the DOE inventory of enriched stable isotopes. Chemical and pyrochemical techniques are used to prepare enriched stable isotopes from this inventory in the desired chemical form. Metallurgical, ceramic, or vacuum processing methods are then used to prepare the isotopes in a wide range of physical forms from thin films, foils, and coatings to large fabricated shapes to meet the needs of experimenters. Significant characterization capabilities are also available to assist in the preparation and evaluation of these custom materials. This work is part of the DOE Isotope Program, which recently transferred to the Office of Nuclear Physics, DOE Office of Science, resulting in a stronger emphasis on enabling R&D. This presentation will focus on the custom preparation of enriched stable isotope targets and other research materials.

  10. Accelerator Generation and Thermal Separation (AGATS) of Technetium-99m

    ScienceCinema (OSTI)

    None

    2013-05-28T23:59:59.000Z

    Accelerator Generation and Thermal Separation (AGATS) of Technetium-99m is a linear electron accelerator-based technology for producing medical imaging radioisotopes from a separation process that heats, vaporizes and condenses the desired radioisotope. You can learn more about INL's education programs at http://www.facebook.com/idahonationallaboratory.

  11. Metal volatilization and separation during incineration

    SciTech Connect (OSTI)

    Ho, T.C.; Chu, H.W.; Hopper, J.R. (Lamar Univ., Beaumont, TX (United States). Dept. of Chemical Engineering)

    1993-01-01T23:59:59.000Z

    The US Environmental Protection Agency (US EPA) has reported that metals can account for almost all of the identified risks from a thermal treatment process. Fundamental research leading to better understanding of their behavior and improved control of their emissions is greatly needed. This paper reports studies on metal volatilization and separation during incineration. Metal volatilization studies were carried out in two separate experiments. In the first experiment, the dynamic volatilization characteristics of various metals during the combustion of metal-containing wood pellets were investigated in a high-temperature electric furnace. In addition to uncontrolled volatilization, the potential of employing chemical additives to bind metals and prevent them from volatilizing during combustion was also investigated. The second experiment involved the investigation of metal volatilization characteristics during the thermal treatment of metal-contaminated clay in a fluidized bed unit. The metal species tested in both experiments were compounds of lead and cadmium. Metal capture/separation studies were also carried out in two separate experiments. The first involved the use of sorbents in the combustion chamber to capture metals during the fluidized bed incineration of metal-containing wood pellets. The second experiments, however, employed sorbents to absorb metal vapors in a fluidized-bed waste-heat boiler. The objective of both the experiments is to characterize the metal absorption efficiency associated with the processes.

  12. Separations by supported liquid membrane cascades

    DOE Patents [OSTI]

    Danesi, Pier R. (Clarendon Hills, IL)

    1986-01-01T23:59:59.000Z

    The invention describes a new separation technique which leads to multi-stage operations by the use of a series (a cascade) of alternated carrier-containing supported-liquid membranes. The membranes contain alternatively a liquid cation exchanger extractant and a liquid anion exchanger extractant (or a neutral extractant) as carrier. The membranes are spaced between alternated aqueous electrolytic solutions of different composition which alternatively provide positively charged extractable species and negatively charged (or zero charged) extractable species, of the chemical species to be separated. The alternated aqueous electrolytic solutions in addition to providing the driving force to the process, simultaneously function as a stripping solution from one type of membrane and as an extraction-promoting solution for the other type of membrane. The aqueous electrolytic solutions and the supported liquid membranes are arranged in such a way to provide a continuous process which leads to the continuous enrichment of the species which show the highest permeability coefficients. By virtue of the very high number of stages which can be arranged, even chemical species having very similar chemical behavior (and consequently very similar permeability coefficients) can be completely separated. The invention also provide a way to concentrate the separated species.

  13. Ultimate Isotope Precision for Carbonates Thermo Scientific

    E-Print Network [OSTI]

    Lachniet, Matthew S.

    Ultimate Isotope Precision for Carbonates Thermo Scientific KIEL IV Carbonate Device Part of Thermo integration cycle Ultimate Isotope Precision for Carbonates The Thermo Scientific KIEL IV Carbonate DeviceV Thermo Scientific MAT 253 or the 3-kV DELTA V isotope ratio mass spectrometer meets the requirements

  14. Isotope Cancer Treatment Research at LANL

    ScienceCinema (OSTI)

    Weidner, John; Nortier, Meiring

    2014-06-02T23:59:59.000Z

    Los Alamos National Laboratory has produced medical isotopes for diagnostic and imaging purposes for more than 30 years. Now LANL researchers have branched out into isotope cancer treatment studies. New results show that an accelerator-based approach can produce clinical trial quantities of actinium-225, an isotope that has promise as a way to kill tumors without damaging surrounding healthy cells.

  15. Separations by supported liquid membrane cascades

    DOE Patents [OSTI]

    Danesi, P.R.

    1983-09-01T23:59:59.000Z

    The invention describes a new separation technique which leads to multi-stage operations by the use of a series (a cascade) of alternated carrier-containing supported-liquid cation exchanger extractant and a liquid anion exchanger extractant (or a neutral extractant) as carrier. The membranes are spaced between alternated aqueous electrolytic solutions of different composition which alternatively provide positively charged extractable species and negatively charged (or zero charged) extractable species, of the chemical species to be separated. The alternated aqueous electrolytic solutions in addition to providing the driving force to the process, simultaneously function as a stripping solution from one type of membrane and as an extraction-promoting solution for the other type of membrane. The aqueous electrolytic solution and the supported liquid membranes are arranged to provide a continuous process.

  16. Membrane separation systems---A research and development needs assessment

    SciTech Connect (OSTI)

    Baker, R.W. (Membrane Technology and Research, Inc., Menlo Park, CA (USA)); Cussler, E.L. (Minnesota Univ., Minneapolis, MN (USA). Dept. of Chemical Engineering and Materials Science); Eykamp, W. (California Univ., Berkeley, CA (USA)); Koros, W.J. (Texas Univ., Austin, TX (USA)); Riley, R.L. (Separation Systems Technology, San Diego, CA (USA)); Strathmann, H. (Fraunhofer-Institut fuer Grenzflaech

    1990-04-01T23:59:59.000Z

    Industrial separation processes consume a significant portion of the energy used in the United States. A 1986 survey by the Office of Industrial Programs estimated that about 4.2 quads of energy are expended annually on distillation, drying and evaporation operations. This survey also concluded that over 0.8 quads of energy could be saved in the chemical, petroleum and food industries alone if these industries adopted membrane separation systems more widely. Membrane separation systems offer significant advantages over existing separation processes. In addition to consuming less energy than conventional processes, membrane systems are compact and modular, enabling easy retrofit to existing industrial processes. The present study was commissioned by the Department of Energy, Office of Program Analysis, to identify and prioritize membrane research needs in light of DOE's mission. Each report will be individually cataloged.

  17. CHEMICAL PROCESS RESEARCH AND DEVELOPMENT PROGRAM

    E-Print Network [OSTI]

    Authors, Various

    2013-01-01T23:59:59.000Z

    Biomass Liquefaction Process Engineering Unit (PEU) S.from Coal Conversion Process Condensate Waters," Lawrenceand C. J. King, J. Separ. Process Technol. , ! • 36 (1979);

  18. Preconcentration and separation of analytes in microchannels

    DOE Patents [OSTI]

    Hatch, Anson (Tracy, CA); Singh, Anup K. (Danville, CA); Herr, Amy E. (Fremont, CA); Throckmorton, Daniel J. (Tracy, CA)

    2010-11-09T23:59:59.000Z

    Disclosed herein are methods and devices for preconcentrating and separating analytes such as proteins and polynucleotides in microchannels. As disclosed, at least one size-exclusion polymeric element is adjacent to processing area or an assay area in a microchannel which may be porous polymeric element. The size-exclusion polymeric element may be used to manipulate, e.g. concentrate, analytes in a sample prior to assaying in the assay area.

  19. Straight-line separation of two polyhedra

    E-Print Network [OSTI]

    Wang, Su-Hua

    1992-01-01T23:59:59.000Z

    1992 ABSTRACT Straight-line Separation of Two Polyhedra. (December 1992) Su-Hua Wang, B. S. , National Chiao Tung University, Taiwan, R. O. C Chair of Advisory Committee: Dr. Jan Wolter The development of automated assembly planning systems has... INTRODUCTION I. A Context Assembly planning is the plan generation problem for assembly tasks and plays an important role in manufacturing systems. The goal of the assembly planning process is to find a plan for moving a set of parts which are initially...

  20. Separation Membrane Development (Separation Using Encapsulated Metal Hydride)

    E-Print Network [OSTI]

    Separation Membrane Development (Separation Using Encapsulated Metal Hydride) L. Kit Heung Savannah: The first is to produce a sol-gel encapsulated metal hydride packing material that will a) absorbs hydrogen may be that hydrogen must come from multiple sources. These sources will include renewable (solar

  1. Gas Separation Using Membranes

    E-Print Network [OSTI]

    Koros, W. J.; Paul, D. R.

    1984-01-01T23:59:59.000Z

    constant diffusion coefficient applies to the diffusion process, von Wroblewski showed that the permeability, P, is equal to the product of the solubility and diffusivity coefficients, i.e., D(C 2 P = _N_ -0 (dC/dx) C 1 ) -~-...:..... = OS (4....6 0.15 1.4 ?u ITS OF PERMEABILITY ARE BARRERS. 1 HARRER Such membranes offered flux increases of as much as 50- to 100-fold compared to their I-mil silicone rubber counterpart s. The membranes were typi ca 11 y supported in a plate...

  2. Where does streamwater come from in low-relief forested watersheds? A dual-isotope approach

    SciTech Connect (OSTI)

    Klaus, Julian [Luxembourg Institute of Science and Technology (LIST), Dept. Environmental Research and Innovation, Belvaux (Luxembourg)

    2015-01-01T23:59:59.000Z

    The time and geographic sources of streamwater in low-relief watersheds are poorly understood. This is partly due to the difficult combination of low runoff coefficients and often damped streamwater isotopic signals precluding traditional hydrograph separation and convolution integral approaches. Here we present a dual-isotope approach involving 18O and 2H of water in a low-angle forested watershed to determine streamwater source components and then build a conceptual model of streamflow generation. We focus on three headwater lowland sub-catchments draining the Savannah River Site in South Carolina, USA.

  3. Where does streamwater come from in low-relief forested watersheds? A dual-isotope approach

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Klaus, Julian

    2015-01-01T23:59:59.000Z

    The time and geographic sources of streamwater in low-relief watersheds are poorly understood. This is partly due to the difficult combination of low runoff coefficients and often damped streamwater isotopic signals precluding traditional hydrograph separation and convolution integral approaches. Here we present a dual-isotope approach involving 18O and 2H of water in a low-angle forested watershed to determine streamwater source components and then build a conceptual model of streamflow generation. We focus on three headwater lowland sub-catchments draining the Savannah River Site in South Carolina, USA.

  4. Diffusion in silicon isotope heterostructures

    SciTech Connect (OSTI)

    Silvestri, Hughes Howland

    2004-05-14T23:59:59.000Z

    The simultaneous diffusion of Si and the dopants B, P, and As has been studied by the use of a multilayer structure of isotopically enriched Si. This structure, consisting of 5 pairs of 120 nm thick natural Si and {sup 28}Si enriched layers, enables the observation of {sup 30}Si self-diffusion from the natural layers into the {sup 28}Si enriched layers, as well as dopant diffusion from an implanted source in an amorphous Si cap layer, via Secondary Ion Mass Spectrometry (SIMS). The dopant diffusion created regions of the multilayer structure that were extrinsic at the diffusion temperatures. In these regions, the Fermi level shift due to the extrinsic condition altered the concentration and charge state of the native defects involved in the diffusion process, which affected the dopant and self-diffusion. The simultaneously recorded diffusion profiles enabled the modeling of the coupled dopant and self-diffusion. From the modeling of the simultaneous diffusion, the dopant diffusion mechanisms, the native defect charge states, and the self- and dopant diffusion coefficients can be determined. This information is necessary to enhance the physical modeling of dopant diffusion in Si. It is of particular interest to the modeling of future electronic Si devices, where the nanometer-scale features have created the need for precise physical models of atomic diffusion in Si. The modeling of the experimental profiles of simultaneous diffusion of B and Si under p-type extrinsic conditions revealed that both species are mediated by neutral and singly, positively charged Si self-interstitials. The diffusion of As and Si under extrinsic n-type conditions yielded a model consisting of the interstitialcy and vacancy mechanisms of diffusion via singly negatively charged self-interstitials and neutral vacancies. The simultaneous diffusion of P and Si has been modeled on the basis of neutral and singly negatively charged self-interstitials and neutral and singly positively charged P species. Additionally, the temperature dependence of the diffusion coefficient of Si in Ge was measured over the temperature range of 550 C to 900 C using a buried Si layer in an epitaxially grown Ge layer.

  5. Device and method for separating minerals, carbon and cement additives from fly ash

    DOE Patents [OSTI]

    Link, Thomas A.; Schoffstall, Micael R.; Soong, Yee

    2004-01-27T23:59:59.000Z

    A process for separating organic and inorganic particles from a dry mixture by sizing the particles into isolated fractions, contacting the sized particles to a charged substrate and subjecting the charged particles to an electric field to separate the particles.

  6. Separator material for electrochemical cells

    DOE Patents [OSTI]

    Cieslak, W.R.; Storz, L.J.

    1991-03-26T23:59:59.000Z

    An electrochemical cell is characterized as utilizing an aramid fiber as a separator material. The aramid fibers are especially suited for lithium/thionyl chloride battery systems. The battery separator made of aramid fibers possesses superior mechanical strength, chemical resistance, and is flame retardant.

  7. Separator material for electrochemical cells

    DOE Patents [OSTI]

    Cieslak, Wendy R. (1166 Laurel Loop NE., Albuquerque, NM 87122); Storz, Leonard J. (2215 Ambassador NE., Albuquerque, NM 87112)

    1991-01-01T23:59:59.000Z

    An electrochemical cell characterized as utilizing an aramid fiber as a separator material. The aramid fibers are especially suited for lithium/thionyl chloride battery systems. The battery separator made of aramid fibers possesses superior mechanical strength, chemical resistance, and is flame retardant.

  8. Entrepreneurial separation to transfer technology.

    SciTech Connect (OSTI)

    Fairbanks, Richard R.

    2010-09-01T23:59:59.000Z

    Entrepreneurial separation to transfer technology (ESTT) program is that entrepreneurs terminate their employment with Sandia. The term of the separation is two years with the option to request a third year. Entrepreneurs are guaranteed reinstatement by Sandia if they return before ESTT expiration. Participants may start up or helpe expand technology businesses.

  9. Photonuclear Reaction Cross Sections for Gallium Isotopes

    E-Print Network [OSTI]

    Serkan Akkoyun; Tuncay Bayram

    2014-09-08T23:59:59.000Z

    The photon induced reactions which are named as photonuclear reactions have a great importance in many field of nuclear, radiation physics and related fields. Since we have planned to perform photonuclear reaction on gallium target with bremmstrahlung photons from clinical linear accelerator in the future, the cross-sections of neutron (photo-neutron ({\\gamma},xn)) and proton (photo-proton ({\\gamma},xn)) productions after photon activation have been calculated by using TALYS 1.2 computer code in this study. The target nucleus has been considered gallium which has two stable isotopes, 69Ga and 71Ga. According to the results, we have seen that the calculations are in harmony in the limited literature values. Furthermore, the pre-equilibrium and compound process contributions to the total cross-section have been investigated.

  10. Chemical and isotopic determination from complex spectra

    SciTech Connect (OSTI)

    Zardecki, A.; Strittmatter, R.B.

    1995-07-01T23:59:59.000Z

    Challenges for proliferation detection include remote, high- sensitivity detection of chemical effluents from suspect facilities and enhanced detection sensitivity for nuclear material. Both the identification of chemical effluents with lidar and enhanced nuclear material detection from radiation sensors involve determining constituents from complex spectra. In this paper, we extend techniques used to analyze time series to the analysis of spectral data. Pattern identification methods are applied to spectral data for domains where standard matrix inversion may not be suitable because of detection statistics. We use a feed-forward, back-propagation neural network in which the nodes of the input layer are fed with the observed spectral data. The nodes of the output layer contain the identification and concentration of the isotope or chemical effluent the sensor is to identify. We will discuss the neural network architecture, together with preliminary results obtained from the training process.

  11. Ab Initio Nuclear Structure and Reaction Calculations for Rare Isotopes

    SciTech Connect (OSTI)

    Draayer, Jerry P [Louisiana State University

    2014-09-28T23:59:59.000Z

    We have developed a novel ab initio symmetry-adapted no-core shell model (SA-NCSM), which has opened the intermediate-mass region for ab initio investigations, thereby providing an opportunity for first-principle symmetry-guided applications to nuclear structure and reactions for nuclear isotopes from the lightest p-shell systems to intermediate-mass nuclei. This includes short-lived proton-rich nuclei on the path of X-ray burst nucleosynthesis and rare neutron-rich isotopes to be produced by the Facility for Rare Isotope Beams (FRIB). We have provided ab initio descriptions of high accuracy for low-lying (including collectivity-driven) states of isotopes of Li, He, Be, C, O, Ne, Mg, Al, and Si, and studied related strong- and weak-interaction driven reactions that are important, in astrophysics, for further understanding stellar evolution, X-ray bursts and triggering of s, p, and rp processes, and in applied physics, for electron and neutrino-nucleus scattering experiments as well as for fusion ignition at the National Ignition Facility (NIF).

  12. Separations and Actinide Science -- 2005 Roadmap

    SciTech Connect (OSTI)

    Not Available

    2005-09-01T23:59:59.000Z

    The Separations and Actinide Science Roadmap presents a vision to establish a separations and actinide science research (SASR) base composed of people, facilities, and collaborations and provides new and innovative nuclear fuel cycle solutions to nuclear technology issues that preclude nuclear proliferation. This enabling science base will play a key role in ensuring that Idaho National Laboratory (INL) achieves its long-term vision of revitalizing nuclear energy by providing needed technologies to ensure our nation's energy sustainability and security. To that end, this roadmap suggests a 10-year journey to build a strong SASR technical capability with a clear mission to support nuclear technology development. If nuclear technology is to be used to satisfy the expected growth in U.S. electrical energy demand, the once-through fuel cycle currently in use should be reconsidered. Although the once-through fuel cycle is cost-effective and uranium is inexpensive, a once-through fuel cycle requires long-term disposal to protect the environment and public from long-lived radioactive species. The lack of a current disposal option (i.e., a licensed repository) has resulted in accumulation of more than 50,000 metric tons of spent nuclear fuel. The process required to transition the current once-through fuel cycle to full-recycle will require considerable time and significant technical advancement. INL's extensive expertise in aqueous separations will be used to develop advanced separations processes. Computational chemistry will be expanded to support development of future processing options. In the intermediate stage of this transition, reprocessing options will be deployed, waste forms with higher loading densities and greater stability will be developed, and transmutation of long-lived fission products will be explored. SASR will support these activities using its actinide science and aqueous separations expertise. In the final stage, full recycle will be enabled by advanced reactors and reprocessing methods based on pyrochemical methods and by using different fuel cycles that do not readily produce plutonium. SASR will facilitate the deployment of advanced pyrochemical separation technology and support development of reprocessing of thorium-based reactor fuels.

  13. Development of an Electrochemical Separator and Compressor

    SciTech Connect (OSTI)

    Trent Molter

    2011-04-28T23:59:59.000Z

    Global conversion to sustainable energy is likely to result in a hydrogen-based economy that supports U.S. energy security objectives while simultaneously avoiding harmful carbon emissions. A key hurdle to successful implementation of a hydrogen economy is the low-cost generation, storage, and distribution of hydrogen. One of the most difficult requirements of this transformation is achieving economical, high density hydrogen storage in passenger vehicles. Transportation applications may require compression and storage of high purity hydrogen up to 12,000 psi. Hydrogen production choices range from centralized low-pressure generation of relatively impure gas in large quantities from steam-methane reformer plants to distributed generation of hydrogen under moderate pressure using water electrolysis. The Electrochemical Hydrogen Separator + Compressor (EHS+C) technology separates hydrogen from impurities and then compresses it to high pressure without any moving parts. The Phase I effort resulted in the construction and demonstration of a laboratory-scale hardware that can separate and compress hydrogen from reformate streams. The completion of Phase I has demonstrated at the laboratory scale the efficient separation and compression of hydrogen in a cost effective manner. This was achieved by optimizing the design of the Electrochemical Hydrogen Compression (EHC) cell hardware and verified by parametric testing in single cell hardware. A broad range of commercial applications exist for reclamation of hydrogen. One use this technology would be in combination with commercial fuel cells resulting in a source of clean power, heat, and compressed hydrogen. Other applications include the reclamation of hydrogen from power plants and other industrial equipment where it is used for cooling, recovery of process hydrogen from heat treating processes, and semiconductor fabrication lines. Hydrogen can also be recovered from reformate streams and cryogenic boil-offs using this technology.

  14. SEPARATION FROM EMPLOYMENT RESIGNATION & RETIREMENT

    E-Print Network [OSTI]

    Su, Xiao

    payment of wages. Faculty members participating in the Faculty Early Retirement Program (FERPSEPARATION FROM EMPLOYMENT RESIGNATION & RETIREMENT HUMAN RESOURCES POLICY Human Resources | One SUBJECT: SEPARATION FROM EMPLOYMENT - RESIGNATION & RETIREMENT DATE: March 2007 I. PURPOSE / DESCRIPTION

  15. Chromatographic Separations of Enantiomers and Underivatized Oligosaccharides

    SciTech Connect (OSTI)

    Ying Liu

    2004-12-19T23:59:59.000Z

    My graduate research has focused on separation science and bioanalytical analysis, which emphasized in method development. It includes three major areas: enantiomeric separations using high performance liquid chromatography (HPLC), Super/subcritical fluid chromatography (SFC), and capillary electrophoresis (CE); drug-protein binding behavior studies using CE; and carbohydrate analysis using liquid chromatograph-electrospray ionization mass spectrometry (LC-ESI-MS). Enantiomeric separations continue to be extremely important in the pharmaceutical industry. An in-depth evaluation of the enantiomeric separation capabilities of macrocyclic glycopeptides CSPs with SFC mobile phases was investigated using a set of over 100 chiral compounds. It was found that the macrocyclic based CSPs were able to separate enantiomers of various compounds with different polarities and functionalities. Seventy percent of all separations were achieved in less than 4 min due to the high flow rate (4.0 ml/min) that can be used in SFC. Drug-protein binding is an important process in determining the activity and fate of a drug once it enters the body. Two drug/protein systems have been studied using frontal analysis CE method. More sensitive fluorescence detection was introduced in this assay, which overcame the problem of low sensitivity that is common when using UV detection for drug-protein studies. In addition, the first usage of an argon ion laser with 257 nm beam coupled with CCD camera as a frontal analysis detection method enabled the simultaneous observation of drug fluorescence as well as the protein fluorescence. LC-ESI-MS was used for the separation and characterization of underivatized oligosaccharide mixtures. With the limits of detection as low as 50 picograms, all individual components of oligosaccharide mixtures (up to 11 glucose-units long) were baseline resolved on a Cyclobond I 2000 column and detected using ESI-MS. This system is characterized by high chromatographic resolution, high column stability, and high sensitivity. In addition, this method showed potential usefulness for the sensitive and quick analysis of hydrolysis products of polysaccharides, and for trace level analysis of individual oligosaccharides or oligosaccharide isomers from biological systems.

  16. Stable Isotope Signatures for Microbial Forensics

    SciTech Connect (OSTI)

    Kreuzer, Helen W.

    2012-01-03T23:59:59.000Z

    The isotopic distribution of the atoms composing the molecules of microorganisms is a function of the substrates used by the organisms. The stable isotope content of an organism is fixed so long as no further substrate consumption and biosynthesis occurs, while the radioactive isotopic content decays over time. The distribution of stable isotopes of C, N, O and H in heterotrophic microorganisms is a direct function of the culture medium, and therefore the stable isotope composition can be used to associate samples with potential culture media and also with one another. The 14C content depends upon the 14C content, and therefore the age, of the organic components of the culture medium, as well as on the age of the culture itself. Stable isotope signatures can thus be used for sample matching, to associate cultures with specific growth media, and to predict characteristics of growth media.

  17. Developing the Sandia National Laboratories transportation infrastructure for isotope products and wastes

    SciTech Connect (OSTI)

    Trennel, A.J.

    1995-12-31T23:59:59.000Z

    Certain radioactive isotopes for North American and especially the United States` needs are enormously important to the medical community and their numerous patients. The most important medical isotope is {sup 99}Mo, which is currently manufactured by Nordion International Inc. in a single, aging reactor operated by Atomic Energy of Canada, Ltd. The reactor`s useful life is expected to end at the turn of the century. Production loss because of reactor shutdown possibilities prompted the US Congress to direct the DOE to provide for a US backup source for this crucial isotope. The SNL Annular Core Research Reactor (ACRR) was evaluated as a site to provide {sup 99}Mo initially and other isotopes that can be economically extracted from the process. Medical isotope production at SNL is a new venture in manufacturing. Should SNL be selected and the project reach the manufacturing stage, SNL would expect to service up to 30% of the US market under normal circumstances as a backup to the Canadian supply with the capability to service 100% should the need arise. The demand for {sup 99}Mo increases each year; hence, the proposed action accommodates growth in demand to meet this increase. The proposed project would guarantee the supply of medical isotopes would continue if either the irradiation or processing activities in Canada were interrupted.

  18. Metal separations using aqueous biphasic partitioning systems

    SciTech Connect (OSTI)

    Chaiko, D.J.; Zaslavsky, B.; Rollins, A.N.; Vojta, Y.; Gartelmann, J.; Mego, W. [Argonne National Lab., IL (United States). Chemical Technology Div.

    1996-05-01T23:59:59.000Z

    Aqueous biphasic extraction (ABE) processes offer the potential for low-cost, highly selective separations. This countercurrent extraction technique involves selective partitioning of either dissolved solutes or ultrafine particulates between two immiscible aqueous phases. The extraction systems that the authors have studied are generated by combining an aqueous salt solution with an aqueous polymer solution. They have examined a wide range of applications for ABE, including the treatment of solid and liquid nuclear wastes, decontamination of soils, and processing of mineral ores. They have also conducted fundamental studies of solution microstructure using small angle neutron scattering (SANS). In this report they review the physicochemical fundamentals of aqueous biphase formation and discuss the development and scaleup of ABE processes for environmental remediation.

  19. EIS-0249: Medical Isotopes Production Project

    Broader source: Energy.gov [DOE]

    This EIS evaluates the potential environmental impacts of a proposal to establish a production capability for molybdenum-99 (Mo-99) and related medical isotopes.

  20. Integration of Nontraditional Isotopic Systems Into Reaction...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Water-Rock Interaction, and Impacts of Water Chemistry on Reservoir Sustainability Integration of Nontraditional Isotopic Systems Into Reaction-Transport Models of EGS For...

  1. Atom trap trace analysis of krypton isotopes

    SciTech Connect (OSTI)

    Bailey, K.; Chen, C. Y.; Du, X.; Li, Y. M.; Lu, Z.-T.; O'Connor, T. P.; Young, L.

    1999-11-17T23:59:59.000Z

    A new method of ultrasensitive isotope trace analysis has been developed. This method, based on the technique of laser manipulation of neutral atoms, has been used to count individual {sup 85}Kr and {sup 81}Kr atoms present in a natural krypton gas sample with isotopic abundances in the range of 10{sup {minus}11} and 10{sup {minus}13}, respectively. This method is free of contamination from other isotopes and elements and can be applied to several different isotope tracers for a wide range of applications. The demonstrated detection efficiency is 1 x 10{sup {minus}7}. System improvements could increase the efficiency by many orders of magnitude.

  2. Stable Isotope Fractionations in Biogeochemical Reactive Transport

    E-Print Network [OSTI]

    Druhan, Jennifer Lea

    2012-01-01T23:59:59.000Z

    34 S fractionation . Summary A mesoscale study of isotopicion exchange and ! 44 Ca . A mesoscale study of isotopicmodeling and ! 34 S . A mesoscale study of isotopic

  3. Method for isotope enrichment by photoinduced chemiionization

    DOE Patents [OSTI]

    Dubrin, James W. (Walnut Creek, CA)

    1985-01-01T23:59:59.000Z

    Isotope enrichment, particularly .sup.235 U enrichment, is achieved by irradiating an isotopically mixed vapor feed with radiant energy at a wavelength or wavelengths chosen to selectively excite the species containing a desired isotope to a predetermined energy level. The vapor feed if simultaneously reacted with an atomic or molecular reactant species capable of preferentially transforming the excited species into an ionic product by a chemiionization reaction. The ionic product, enriched in the desired isotope, is electrostatically or electromagnetically extracted from the reaction system.

  4. ASME PTC 47 - IGCC performance testing: Air separation issues

    SciTech Connect (OSTI)

    Smith, A.R.

    1998-07-01T23:59:59.000Z

    Air separation units have been incorporated into the designs of many gasification combined cycle projects worldwide for the supply of pressurized oxygen and nitrogen. Pressurized gaseous oxygen at a purity usually above 95% by volume is supplied to the gasification unit to partially oxidized a hydrocarbon feed to yield syngas. Nitrogen streams are used for purging and inerting purposes or for the reactor. Several facilities have incorporated integration of air and/or nitrogen streams between the gas turbine and the air separation unit to improve overall facility cost, power output and efficiency. Gasification processes that are based on air as the oxidant source may also require an air separation unit to supply pressurized nitrogen for inerting and dry fuel transport. This paper reports on the progress of PTC 47's air separation subcommittee in defining test measurement boundaries and performance parameter definitions for the testing of an air separation unit as a subsystem of the gasification combined cycle facility.

  5. Means and method of detection in chemical separation procedures

    DOE Patents [OSTI]

    Yeung, Edward S. (Ames, IA); Koutny, Lance B. (Ames, IA); Hogan, Barry L. (Ames, IA); Cheung, Chan K. (Ames, IA); Ma, Yinfa (Ames, IA)

    1993-03-09T23:59:59.000Z

    A means and method for indirect detection of constituent components of a mixture separated in a chemical separation process. Fluorescing ions are distributed across the area in which separation of the mixture will occur to provide a generally uniform background fluorescence intensity. For example, the mixture is comprised of one or more charged analytes which displace fluorescing ions where its constituent components separate to. Fluorescing ions of the same charge as the charged analyte components cause a displacement. The displacement results in the location of the separated components having a reduced fluorescence intensity to the remainder of the background. Detection of the lower fluorescence intensity areas can be visually, by photographic means and methods, or by automated laser scanning.

  6. Coal liquefaction process with enhanced process solvent

    DOE Patents [OSTI]

    Givens, Edwin N. (Bethlehem, PA); Kang, Dohee (Macungie, PA)

    1984-01-01T23:59:59.000Z

    In an improved coal liquefaction process, including a critical solvent deashing stage, high value product recovery is improved and enhanced process-derived solvent is provided by recycling second separator underflow in the critical solvent deashing stage to the coal slurry mix, for inclusion in the process solvent pool.

  7. O isotopic composition of CaCO3 measured by continuous ow isotope ratio mass spectrometry

    E-Print Network [OSTI]

    d13 C and d18 O isotopic composition of CaCO3 measured by continuous ¯ow isotope ratio mass. This new method streamlines the classical phosphoric acid/calcium carbonate (H3PO4/CaCO3) reaction method XL continuous flow isotope ratio mass spectrometer. Conditions for which the H3PO4/CaCO3 reaction

  8. TA-55: LANL Plutonium-Processing Facilities

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    chemistry; nuclear materials separation, processing, and recovery; plutonium metallurgy, preparation, casting, fabrication, and recovery; machining and metallurgy...

  9. Discovery of Isotopes of Elements with Z $\\ge$ 100

    E-Print Network [OSTI]

    M. Thoennessen

    2012-03-09T23:59:59.000Z

    Currently, 163 isotopes of elements with Z $\\ge$ 100 have been observed and the discovery of these isotopes is discussed here. For each isotope a brief synopsis of the first refereed publication, including the production and identification method, is presented.

  10. Gamma Spectrum from Neutron Capture on Tungsten Isotopes

    E-Print Network [OSTI]

    Hurst, Aaron

    2011-01-01T23:59:59.000Z

    FROM NEUTRON CAPTURE ON TUNGSTEN ISOTOPES A. M. HURST ?1,2 ,capture on the stable tungsten isotopes is presented, withknown decay schemes of the tungsten isotopes from neutron

  11. A TRUEX-based separation of americium from the lanthanides

    SciTech Connect (OSTI)

    Bruce J. Mincher; Nicholas C. Schmitt; Mary E. Case

    2011-03-01T23:59:59.000Z

    Abstract: The inextractability of the actinide AnO2+ ions in the TRUEX process suggests the possibility of a separation of americium from the lanthanides using oxidation to Am(V). The only current method for the direct oxidation of americium to Am(V) in strongly acidic media is with sodium bismuthate. We prepared Am(V) over a wide range of nitric acid concentrations and investigated its solvent extraction behavior for comparison to europium. While a separation is achievable in principal, the presence of macro amounts of cerium competes for the sparingly soluble oxidant and the oxidant itself competes for CMPO complexation. These factors conspire to reduce the Eu/Am separation factor from ~40 using tracer solutions to ~5 for extractions from first cycle raffinate simulant solution. To separate pentavalent americium directly from the lanthanides using the TRUEX process, an alternative oxidizing agent will be necessary.

  12. Neutrino scattering off the stable even-even Mo isotopes

    SciTech Connect (OSTI)

    Balasi, K. G.; Kosmas, T. S.; Divari, P. C. [Theoretical Physics Section, University of Ioannina, GR 45110 Ioannina (Greece)

    2009-11-09T23:59:59.000Z

    Inelastic neutrino-nucleus reaction cross sections are studied focusing on the neutral current processes. Particularly, we investigate the angular and initial neutrino-energy dependence of the differential and integrated cross sections for low and intermediate energies of the incoming neutrino. The nuclear wave functions for the initial and final nuclear states are constructed in the context of the quasi-particle random phase approximation (QRPA) tested on the reproducibility of the low-lying energy spectrum. The results presented here refer to the isotopes Mo{sup 92}, Mo{sup 94}, Mo{sup 96}, Mo{sup 98} and Mo{sup 100}. These isotopes could play a significant role in supernova neutrino detection in addition to their use in double-beta and neutrinoless double-beta decay experiments (e.g. MOON, NEMO III)

  13. Europium Isotopic Abundances in Very Metal-poor Stars

    E-Print Network [OSTI]

    Christopher Sneden; John J. Cowan; James E. Lawler; Scott Burles; Timothy C. Beers; George M. Fuller

    2002-01-28T23:59:59.000Z

    Europium isotopic abundance fractions are reported for the very metal-poor, neutron-capture-rich giant stars CS 22892-052, HD 115444, and BD +17 3248. The abundance fractions, derived from analysis of several strong Eu II lines appearing in high-resolution spectra of these stars, are in excellent agreement with each other and with their values in the Solar System: fraction(\\iso{Eu}{151}) ~= fraction(\\iso{Eu}{153}) ~= 0.5. Detailed abundance studies of very metal-poor stars have previously shown that the total elemental abundances of stable atoms with atomic numbers z >= 56 typically match very closely those of a scaled solar-system r-process abundance distribution. The present results for the first time extend this agreement to the isotopic level.

  14. The Isotopic Mixture of Barium in the Metal-poor Subgiant HD 140283

    E-Print Network [OSTI]

    David L. Lambert; Carlos Allende Prieto

    2002-05-22T23:59:59.000Z

    Analyses of the abundances of neutron-capture elements have led to the belief that these elements in metal-poor stars are r-process products with relative abundances closely resembling those found in the solar system. This picture was challenged by Magain (1995), who found that a pure r-process mix of the barium isotopes was inconsistent with the mix of odd to even barium isotopes derived from analysis of the Ba II line at 4554 A in the spectrum of the metal-poor subgiant HD 140283. In this paper, we address Magain's challenge using new high resolution high signal-to-noise spectra of HD 140283, and find, in contrast to his result, that a solar-like r-process isotopic mixture provides a fair fit to the observed 4554 A profile.

  15. Laser vaporization/ionization interface for coupling microscale separation techniques with mass spectrometry

    DOE Patents [OSTI]

    Yeung, E.S.; Chang, Y.C.

    1999-06-29T23:59:59.000Z

    The present invention provides a laser-induced vaporization and ionization interface for directly coupling microscale separation processes to a mass spectrometer. Vaporization and ionization of the separated analytes are facilitated by the addition of a light-absorbing component to the separation buffer or solvent. 8 figs.

  16. Separating the Minor Actinides Through Advances in Selective Coordination Chemistry

    SciTech Connect (OSTI)

    Lumetta, Gregg J.; Braley, Jenifer C.; Sinkov, Sergey I.; Carter, Jennifer C.

    2012-08-22T23:59:59.000Z

    This report describes work conducted at the Pacific Northwest National Laboratory (PNNL) in Fiscal Year (FY) 2012 under the auspices of the Sigma Team for Minor Actinide Separation, funded by the U.S. Department of Energy Office of Nuclear Energy. Researchers at PNNL and Argonne National Laboratory (ANL) are investigating a simplified solvent extraction system for providing a single-step process to separate the minor actinide elements from acidic high-level liquid waste (HLW), including separating the minor actinides from the lanthanide fission products.

  17. Tropical Pacific nutrient dynamics in the modern and pleistocene ocean : insights from the nitrogen isotope system

    E-Print Network [OSTI]

    Rafter, Patrick Anthony

    2009-01-01T23:59:59.000Z

    nitrogen isotopes, an enrichment that is conventionallyisotopes upon denitrification also imparts a strong isotopic enrichment

  18. Novel, Ceramic Membrane System For Hydrogen Separation

    SciTech Connect (OSTI)

    Elangovan, S.

    2012-12-31T23:59:59.000Z

    Separation of hydrogen from coal gas represents one of the most promising ways to produce alternative sources of fuel. Ceramatec, teamed with CoorsTek and Sandia National Laboratories has developed materials technology for a pressure driven, high temperature proton-electron mixed conducting membrane system to remove hydrogen from the syngas. This system separates high purity hydrogen and isolates high pressure CO{sub 2} as the retentate, which is amenable to low cost capture and transport to storage sites. The team demonstrated a highly efficient, pressure-driven hydrogen separation membrane to generate high purity hydrogen from syngas using a novel ceramic-ceramic composite membrane. Recognizing the benefits and limitations of present membrane systems, the all-ceramic system has been developed to address the key technical challenges related to materials performance under actual operating conditions, while retaining the advantages of thermal and process compatibility offered by the ceramic membranes. The feasibility of the concept has already been demonstrated at Ceramatec. This project developed advanced materials composition for potential integration with water gas shift rectors to maximize the hydrogenproduction.

  19. Separations Technology for Clean Water and Energy

    SciTech Connect (OSTI)

    Jarvinen, Gordon D [Los Alamos National Laboratory

    2012-06-22T23:59:59.000Z

    Providing clean water and energy for about nine billion people on the earth by midcentury is a daunting challenge. Major investments in efficiency of energy and water use and deployment of all economical energy sources will be needed. Separations technology has an important role to play in producing both clean energy and water. Some examples are carbon dioxide capture and sequestration from fossil energy power plants and advanced nuclear fuel cycle scemes. Membrane separations systems are under development to improve the economics of carbon capture that would be required at a huge scale. For nuclear fuel cycles, only the PUREX liquid-liquid extraction process has been deployed on a large scale to recover uranium and plutonium from used fuel. Most current R and D on separations technology for used nuclear fuel focuses on ehhancements to a PUREX-type plant to recover the minor actinides (neptunium, americiu, and curium) and more efficiently disposition the fission products. Are there more efficient routes to recycle the actinides on the horizon? Some new approaches and barriers to development will be briefly reviewed.

  20. FY 2009 Progress: Process Monitoring Technology Demonstration at PNNL

    SciTech Connect (OSTI)

    Arrigo, Leah M.; Christensen, Ronald N.; Fraga, Carlos G.; Liezers, Martin; Peper, Shane M.; Thomas, Elizabeth M.; Bryan, Samuel A.; Douglas, Matthew; Laspe, Amy R.; Lines, Amanda M.; Peterson, James M.; Ward, Rebecca M.; Casella, Amanda J.; Duckworth, Douglas C.; Levitskaia, Tatiana G.; Orton, Christopher R.; Schwantes, Jon M.

    2009-12-01T23:59:59.000Z

    Pacific Northwest National Laboratory (PNNL) is developing and demonstrating three technologies designed to assist in the monitoring of reprocessing facilities in near-real time. These technologies include 1) a multi-isotope process monitor (MIP), 2) a spectroscopy-based monitor that uses UV-Vis-NIR (ultraviolet-visible-near infrared) and Raman spectrometers, and 3) an electrochemically modulated separations approach (EMS). The MIP monitor uses gamma spectroscopy and pattern recognition software to identify off-normal conditions in process streams. The UV-Vis-NIR and Raman spectroscopic monitoring continuously measures chemical compositions of the process streams including actinide metal ions (uranium, plutonium, neptunium), selected fission products, and major cold flow sheet chemicals. The EMS approach provides an on-line means for separating and concentrating elements of interest out of complex matrices prior to detection via nondestructive assay by gamma spectroscopy or destructive analysis with mass spectrometry. A general overview of the technologies and ongoing demonstration results are described in this report.

  1. Advanced Nanostructured Molecular Sieves for Energy Efficient Industrial Separations

    SciTech Connect (OSTI)

    Kunhao Li, Michael Beaver

    2012-01-18T23:59:59.000Z

    Due to the very small relative volatility difference between propane and propylene, current propane/propylene separation by distillation requires very tall distillation towers (150-250 theoretical plates) and large reflux ratios (up to 15), which is considered to be the most energy consuming large-scale separation process. Adsorptive separation processes are widely considered to be more energy-efficient alternatives to distillation. However, slow diffusion kinetics/mass transport rate through the adsorbent bed often limits the performance of such processes, so further improvements are possible if intra-particle mass transfer rates can be improved. Rive Technology, Inc. is developing and commercializing its proprietary mesoporous zeolite technology for catalysis and separation. With well-controlled intracrystalline mesoporosity, diffusion kinetics through such mesoporous zeolite based catalysts is much improved relative to conventional zeolites, leading to significantly better product selectivity. This 'proof-of-principle' project (DE-EE0003470) is intended to demonstrate that Rive mesoporous zeolite technology can be extended and applied in adsorptive propane/propylene separation and lead to significant energy saving compared to the current distillation process. In this project, the mesoporous zeolite Y synthesis technology was successfully extended to X and A zeolites that are more relevant to adsorbent applications. Mesoporosity was introduced to zeolite X and A for the first time while maintaining adequate adsorption capacity. Zeolite adsorbents were tested for liquid phase separation performance using a pulse flow test unit and the test results show that the separation selectivity of the mesoporous zeolite adsorbent is much closer to optimal for a Simulated Moving Bed (SMB) separation process and the enhanced mesoporosity lead to >100% increase of overall mass transport rate for propane and propylene. These improvements will significantly improve the performance of an adsorptive separation unit for propane/propylene separation compared with traditional zeolite adsorbents. The enhanced transport will allow for more efficient utilization of a given adsorbent inventory by reducing process cycle time, allowing a faster production rate with a fixed amount of adsorbent or smaller adsorbent inventory at a fixed production rate. Smaller adsorbent inventory would also lead to significant savings in the capital cost due to smaller footprint of the equipment. Energy consumption calculation, based on the pulse test results for rived NaX zeolite adsorbent, of a hypothetical moderate-scale SMB propane/propylene separation plant that processes 6000 BPSD refinery grade propylene (70% propylene) will consume about 60-80% less energy (both re-boiler and condenser duties) compared to a C3 splitter that process the same amount of feed. This energy saving also translates to a reduction of 30,000-35,000 tons of CO2 emission per year at this moderate processing rate. The enhancement of mass transport achievable by introduction of controlled mesoporosity to the zeolite also opens the door for the technology to be applied to several other adsorption separation processes such as the separation of xylene isomers by SMB, small- and large scale production of O2/N2 from air by pressure swing adsorption, the separation of CO2 from natural gas at natural gas wellheads, and the purification of ultra-high purity H2 from the off gas produced by steam-methane-reforming.

  2. Spatial periphery of lithium isotopes

    SciTech Connect (OSTI)

    Galanina, L. I., E-mail: galan_lidiya@mail.ru; Zelenskaja, N. S. [Moscow State University, Skobeltsyn Institute of Nuclear Physics (Russian Federation)

    2013-12-15T23:59:59.000Z

    The spatial structure of lithium isotopes is studied with the aid of the charge-exchange and (t, p) reactions on lithium nuclei. It is shown that an excited isobaric-analog state of {sup 6}Li (0{sup +}, 3.56MeV) has a halo structure formed by a proton and a neutron, that, in the {sup 9}Li nucleus, there is virtually no neutron halo, and that {sup 11}Li is a Borromean nucleus formed by a {sup 9}Li core and a two-neutron halo manifesting itself in cigar-like and dineutron configurations.

  3. Stable carbon and nitrogen isotope enrichment in primate tissues

    E-Print Network [OSTI]

    Crowley, Brooke E.; Carter, Melinda L.; Karpanty, Sarah M.; Zihlman, Adrienne L.; Koch, Paul L.; Dominy, Nathaniel J.

    2010-01-01T23:59:59.000Z

    carbon and nitrogen isotope enrichment in primate tissuesfactor (a) and isotope enrichment values (e), which provideisotope values from different modern primate tissues. Additionally, using these mean apparent enrichment

  4. CRAD, Engineering - Oak Ridge National Laboratory High Flux Isotope...

    Broader source: Energy.gov (indexed) [DOE]

    Engineering - Oak Ridge National Laboratory High Flux Isotope Reactor Contractor ORR CRAD, Engineering - Oak Ridge National Laboratory High Flux Isotope Reactor Contractor ORR...

  5. CRAD, Engineering - Oak Ridge National Laboratory High Flux Isotope...

    Broader source: Energy.gov (indexed) [DOE]

    Oak Ridge National Laboratory High Flux Isotope Reactor CRAD, Engineering - Oak Ridge National Laboratory High Flux Isotope Reactor February 2007 A section of Appendix C to DOE G...

  6. aluminium isotopes: Topics by E-print Network

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    CERN Preprints Summary: Currently, 31 actinium, 31 thorium, 28 protactinium, and 23 uranium isotopes have so far been observed; the discovery of these isotopes is discussed. For...

  7. americium isotopes: Topics by E-print Network

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    CERN Preprints Summary: Currently, 31 actinium, 31 thorium, 28 protactinium, and 23 uranium isotopes have so far been observed; the discovery of these isotopes is discussed. For...

  8. activated bismuth isotopes: Topics by E-print Network

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    CERN Preprints Summary: Currently, 31 actinium, 31 thorium, 28 protactinium, and 23 uranium isotopes have so far been observed; the discovery of these isotopes is discussed. For...

  9. astatine isotopes: Topics by E-print Network

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    CERN Preprints Summary: Currently, 31 actinium, 31 thorium, 28 protactinium, and 23 uranium isotopes have so far been observed; the discovery of these isotopes is discussed. For...

  10. A Helium Isotope Perspective On The Dixie Valley, Nevada, Hydrothermal...

    Open Energy Info (EERE)

    Helium Isotope Perspective On The Dixie Valley, Nevada, Hydrothermal System Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal Article: A Helium Isotope...

  11. Isotopic Analysis- Fluid At Dixie Valley Geothermal Area (Kennedy...

    Open Energy Info (EERE)

    geothermal resources with deep, fault hosted permeable fluid flow pathways and the helium Isotopic composition of the surface fluids. The authors suggest that helium isotopes...

  12. Fractionation of Oxygen Isotopes in Phosphate during its Interactions...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Fractionation of Oxygen Isotopes in Phosphate during its Interactions with Iron Oxides. Fractionation of Oxygen Isotopes in Phosphate during its Interactions with Iron Oxides....

  13. applied isotope techniques: Topics by E-print Network

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    M. 22 Applied Radiation and Isotopes 55 (2001) 707713 Bronchial dosimeter for radon progeny Biology and Medicine Websites Summary: Applied Radiation and Isotopes 55 (2001)...

  14. Phosphazene membranes for gas separations

    DOE Patents [OSTI]

    Stewart, Frederick F.; Harrup, Mason K.; Orme, Christopher J.; Luther, Thomas A.

    2006-07-11T23:59:59.000Z

    A polyphosphazene having a glass transition temperature ("Tg") of approximately -20.degree. C. or less. The polyphosphazene has at least one pendant group attached to a backbone of the polyphosphazene, wherein the pendant group has no halogen atoms. In addition, no aromatic groups are attached to an oxygen atom that is bound to a phosphorus atom of the backbone. The polyphosphazene may have a Tg ranging from approximately -100.degree. C. to approximately -20.degree. C. The polyphosphazene may be selected from the group consisting of poly[bis-3-phenyl-1-propoxy)phosphazene], poly[bis-(2-phenyl-1-ethoxy)phosphazene], poly[bis-(dodecanoxypolyethoxy)-phosphazene], and poly[bis-(2-(2-(2-.omega.-undecylenyloxyethoxy)ethoxy)ethoxy)phosphazene]. The polyphosphazene may be used in a separation membrane to selectively separate individual gases from a gas mixture, such as to separate polar gases from nonpolar gases in the gas mixture.

  15. Conjugates of Actinide Chelator-Magnetic Nanoparticles for Used Fuel Separation Technology

    SciTech Connect (OSTI)

    Qiang, You; Paszczynski, Andrzej; Rao, Linfeng

    2011-10-30T23:59:59.000Z

    The actinide separation method using magnetic nanoparticles (MNPs) functionalized with actinide specific chelators utilizes the separation capability of ligand and the ease of magnetic separation. This separation method eliminated the need of large quantity organic solutions used in the liquid-liquid extraction process. The MNPs could also be recycled for repeated separation, thus this separation method greatly reduces the generation of secondary waste compared to traditional liquid extraction technology. The high diffusivity of MNPs and the large surface area also facilitate high efficiency of actinide sorption by the ligands. This method could help in solving the nuclear waste remediation problem.

  16. Real-Time Detection Methods to Monitor TRU Compositions in UREX+Process Streams

    SciTech Connect (OSTI)

    McDeavitt, Sean; Charlton, William; Indacochea, J Ernesto; taleyarkhan, Rusi; Pereira, Candido

    2013-03-01T23:59:59.000Z

    The U.S. Department of Energy has developed advanced methods for reprocessing spent nuclear fuel. The majority of this development was accomplished under the Advanced Fuel Cycle Initiative (AFCI), building on the strong legacy of process development R&D over the past 50 years. The most prominent processing method under development is named UREX+. The name refers to a family of processing methods that begin with the Uranium Extraction (UREX) process and incorporate a variety of other methods to separate uranium, selected fission products, and the transuranic (TRU) isotopes from dissolved spent nuclear fuel. It is important to consider issues such as safeguards strategies and materials control and accountability methods. Monitoring of higher actinides during aqueous separations is a critical research area. By providing on-line materials accountability for the processes, covert diversion of the materials streams becomes much more difficult. The importance of the nuclear fuel cycle continues to rise on national and international agendas. The U.S. Department of Energy is evaluating and developing advanced methods for safeguarding nuclear materials along with instrumentation in various stages of the fuel cycle, especially in material balance areas (MBAs) and during reprocessing of used nuclear fuel. One of the challenges related to the implementation of any type of MBA and/or reprocessing technology (e.g., PUREX or UREX) is the real-time quantification and control of the transuranic (TRU) isotopes as they move through the process. Monitoring of higher actinides from their neutron emission (including multiplicity) and alpha signatures during transit in MBAs and in aqueous separations is a critical research area. By providing on-line real-time materials accountability, diversion of the materials becomes much more difficult. The objective of this consortium was to develop real time detection methods to monitor the efficacy of the UREX+ process and to safeguard the separated TRUs against unlawful diversion from within a processing facility. To achieve this, a comprehensive strategy was implemented to incorporate traditional detectors and advanced Tensioned Metastable Fluid (TMFD) metastable fluid detectors (developed, in part, under this project) into a novel detector assembly coupled to the UREX+ centrifugal contactor array. The sections below provide a brief summary of the technical achievements completed during this project. The principal outcomes are documented in more complete details contained the doctoral dissertations and masters theses, journal papers, conference proceedings and additional items for more than the 35 publications that are listed in the program bibliography in Section 3.

  17. Advanced Mass Spectrometers for Hydrogen Isotope Analyses

    SciTech Connect (OSTI)

    Chastagner, P.

    2001-08-01T23:59:59.000Z

    This report is a summary of the results of a joint Savannah River Laboratory (SRL) - Savannah River Plant (SRP) ''Hydrogen Isotope Mass Spectrometer Evaluation Program''. The program was undertaken to evaluate two prototype hydrogen isotope mass spectrometers and obtain sufficient data to permit SRP personnel to specify the mass spectrometers to replace obsolete instruments.

  18. Positive and inverse isotope effect on superconductivity

    E-Print Network [OSTI]

    Tian De Cao

    2009-09-04T23:59:59.000Z

    This article improves the BCS theory to include the inverse isotope effect on superconductivity. An affective model can be deduced from the model including electron-phonon interactions, and the phonon-induced attraction is simply and clearly explained on the electron Green function. The focus of this work is on how the positive or inverse isotope effect occurs in superconductors.

  19. MARK E. CONRAD Center for Isotope Geochemistry

    E-Print Network [OSTI]

    Ajo-Franklin, Jonathan

    with stable isotopes, fate and transport of groundwater contaminants, vadose zone hydrology, metal uptake by lichens, paleoclimatic patterns in California and stable isotope systematics of clay minerals. Geologist of gold property in the Mother Lode of California. Exploration Geologist (Anaconda Minerals Company; 6

  20. The Quest for the Heaviest Uranium Isotope

    E-Print Network [OSTI]

    S. Schramm; D. Gridnev; D. V. Tarasov; V. N. Tarasov; W. Greiner

    2012-01-17T23:59:59.000Z

    We study Uranium isotopes and surrounding elements at very large neutron number excess. Relativistic mean field and Skyrme-type approaches with different parametrizations are used in the study. Most models show clear indications for isotopes that are stable with respect to neutron emission far beyond N=184 up to the range of around N=258.