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Sample records for chemical ion exchangers

  1. Contamination weeping: A chemical ion exchange model

    SciTech Connect

    Chambers, W.B.; Doughty, D.H.; Jones, H.D.T.; Martinez, S.L.; Bennett, P.C.

    1991-01-01

    Experiments have been conducted to determine the applicability of a chemical ion-exchange model to characterize the problem of nuclear fuel transportation cask contamination and release ( weeping''). Surface charge characteristics of Cr{sub 2}O{sub 3} and stainless steel (304) powders have been measured to determine the potential for ion exchange at metal oxide -- aqueous interfaces. The solubility of pool contaminant Co and Cs electrolytes at varying pH and the adsorption characteristics of these ions on Cr{sub 2}O{sub 3} and stainless steel powders in aqueous slurries have been studied. Experiments show that Co ions do reversibly adsorb on these powder surfaces and, more specifically, that adsorption occurs in the nominal pH range (pH = 4--6) of a boric acid-moderated spent fuel pool. Desorption has been demonstrated to occur at pH {le} 3. Cs ions also have been shown to have an affinity for these surfaces although the reversibility of Cs{sup +} bonding by H{sup +} ion exchange has not been fully demonstrated. These results have significant implications for effective decontamination and coating processes used on nuclear fuel transportation casks. 9 refs., 5 figs., 1 tab.

  2. 10 CFR Appendix E to Part 110 - Illustrative List of Chemical Exchange or Ion Exchange Enrichment Plant Equipment and Components...

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... between the isotopes of uranium causes small changes in chemical reaction equilibria that can be used as a... 10 Energy 2 2013-01-01 2013-01-01 false Illustrative List of Chemical Exchange or Ion Exchange.... 110, App. E Appendix E to Part 110—Illustrative List of Chemical Exchange or Ion Exchange...

  3. 10 CFR Appendix E to Part 110 - Illustrative List of Chemical Exchange or Ion Exchange Enrichment Plant Equipment and Components...

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... between the isotopes of uranium causes small changes in chemical reaction equilibria that can be used as a... 10 Energy 2 2011-01-01 2011-01-01 false Illustrative List of Chemical Exchange or Ion Exchange.... 110, App. E Appendix E to Part 110—Illustrative List of Chemical Exchange or Ion Exchange...

  4. 10 CFR Appendix E to Part 110 - Illustrative List of Chemical Exchange or Ion Exchange Enrichment Plant Equipment and Components...

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... between the isotopes of uranium causes small changes in chemical reaction equilibria that can be used as a... 10 Energy 2 2014-01-01 2014-01-01 false Illustrative List of Chemical Exchange or Ion Exchange.... 110, App. E Appendix E to Part 110—Illustrative List of Chemical Exchange or Ion Exchange...

  5. 10 CFR Appendix E to Part 110 - Illustrative List of Chemical Exchange or Ion Exchange Enrichment Plant Equipment and Components...

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... between the isotopes of uranium causes small changes in chemical reaction equilibria that can be used as a... 10 Energy 2 2012-01-01 2012-01-01 false Illustrative List of Chemical Exchange or Ion Exchange.... 110, App. E Appendix E to Part 110—Illustrative List of Chemical Exchange or Ion Exchange...

  6. The chemical precipitation of nickel on ion exchangers and active carbons

    NASA Astrophysics Data System (ADS)

    Khorol'Skaya, S. V.; Zolotukhina, E. V.; Polyanskii, L. N.; Peshkov, S. V.; Kravchenko, T. A.; Krysanov, V. A.

    2010-12-01

    The chemical precipitation of nickel in the form of poorly soluble precipitates in ion exchanger matrices and on active carbons from solutions of nickel chloride and chemical nickel plating electrolytes was studied. The sorption of nickel ions from a solution of nickel chloride occurs most effectively on Purolite D24002 macroporous chelate forming ion exchanger, KU-23-15/100 sulfo cation exchanger, and KU-2-8 gel sulfo cation exchanger. Nickel enters sulfo cation exchangers in the form of counterions, and is adsorbed on Purolite D24002 largely because of complex formation. The subsequent precipitation of nickel in the solid state in matrix pores liberates ionogenic centers, which allows repeated sorption cycles to be performed. After three chemical precipitation cycles under static conditions, the amount of nickel is higher by 170-250% than the ion exchange capacity of the sorbents. The electrolyte of chemical nickel plating contains nickel predominantly in the form of negatively charged and neutral complexes with glycine, which cannot form bonds with the matrices under study. It is therefore reasonable to perform sorption at decreased solution pH values.

  7. Adsorption, partition, ion exchange and chemical reaction in batch reactors or in columns — A review

    NASA Astrophysics Data System (ADS)

    Schweich, D.; Sardin, M.

    The role of linear or non-linear adsorption, mass transfer kinetics, chemical reactions and ion exchange in column tracer experiments is qualitatively dealt with. The similarity of elution curves is emphasized even for very different phenomena. Some experimental procedures are proposed to point out the principal physico-chemical phenomenon which is responsible for the shape of the adsorption isotherm deduced from batch or column experiments.

  8. Chemical modification of corn fiber with ion-exchanging groups

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Pretreated corn fiber was chemically modified with quaternary ammonium group or/and sulfonated with 3-chloro-2-hydroxypropanesulfonic acid under vacuum or at ambient pressure. The soluble fraction was dialyzed through 1 kDa MWCO dialysis tubing and the material retained inside the tubing was filtere...

  9. Ion Exchange Equilibrium and Kinetic Properties of Polyacrylate Films and Applications to Chemical Analysis and Environmental Decontamination

    NASA Technical Reports Server (NTRS)

    Tanner, Stephen P.

    1997-01-01

    One of the goals of the original proposal was to study how cross-linking affects the properties of an ion exchange material(IEM) developed at Lewis Research Center. However, prior to the start of this work, other workers at LERC investigated the effect of cross-linking on the properties of this material. Other than variation in the ion exchange capacity, the chemical characteristics were shown to be independent of the cross-linking agent, and the degree of cross-linking. New physical forms of the film were developed (film, supported film, various sizes of beads, and powder). All showed similar properties with respect to ion exchange equilibria but the kinetics of ion exchange depended on the surface area per unit mass; the powder form of the IEM exchanging much more rapidly than the other forms. The research performed under this grant was directed towards the application of the IEM to the analysis of metal ions at environmental concentrations.

  10. Ion exchange technology assessment report

    SciTech Connect

    Duhn, E.F.

    1992-01-01

    In the execution of its charter, the SRS Ion Exchange Technology Assessment Team has determined that ion exchange (IX) technology has evolved to the point where it should now be considered as a viable alternative to the SRS reference ITP/LW/PH process. The ion exchange media available today offer the ability to design ion exchange processing systems tailored to the unique physical and chemical properties of SRS soluble HLW's. The technical assessment of IX technology and its applicability to the processing of SRS soluble HLW has demonstrated that IX is unquestionably a viable technology. A task team was chartered to evaluate the technology of ion exchange and its potential for replacing the present In-Tank Precipitation and proposed Late Wash processes to remove Cs, Sr, and Pu from soluble salt solutions at the Savannah River Site. This report documents the ion exchange technology assessment and conclusions of the task team.

  11. Ion exchange technology assessment report

    SciTech Connect

    Duhn, E.F.

    1992-12-31

    In the execution of its charter, the SRS Ion Exchange Technology Assessment Team has determined that ion exchange (IX) technology has evolved to the point where it should now be considered as a viable alternative to the SRS reference ITP/LW/PH process. The ion exchange media available today offer the ability to design ion exchange processing systems tailored to the unique physical and chemical properties of SRS soluble HLW`s. The technical assessment of IX technology and its applicability to the processing of SRS soluble HLW has demonstrated that IX is unquestionably a viable technology. A task team was chartered to evaluate the technology of ion exchange and its potential for replacing the present In-Tank Precipitation and proposed Late Wash processes to remove Cs, Sr, and Pu from soluble salt solutions at the Savannah River Site. This report documents the ion exchange technology assessment and conclusions of the task team.

  12. Swelling behavior of ion exchange resins incorporated in tri-calcium silicate cement matrix: I. Chemical analysis

    NASA Astrophysics Data System (ADS)

    Neji, M.; Bary, B.; Le Bescop, P.; Burlion, N.

    2015-12-01

    This paper presents the first part of a theoretical and experimental work aiming at modeling the chemo-mechanical behavior of composites made up of ion exchange resins (IER) solidified in a tri-calcium silicate cement paste (C3S). Because of ion exchange processes, the volume change of the IER may cause internal pressures leading to the degradation of the material. In this study, a predictive modeling is developed for describing the chemical behavior of such material. It is based on thermodynamic equilibria to determine the evolution of the ion exchange processes, and the potential precipitation of portlandite in the composite. In parallel, a phenomenological study has been set up to understand chemical phenomena related to the swelling mechanisms. The model created has been finally implemented in a finite elements software; the simulation of a laboratory test has been performed and the results compared to experimental data.

  13. Quantum Chemical Study of the Water Exchange Mechanism of the Americyl(VI) Aqua Ion.

    PubMed

    Fabrizio, Alberto; Rotzinger, François P

    2016-11-07

    The water exchange reaction of the americyl(VI) aqua ion was investigated with quantum chemical methods, density functional theory (DFT), and wave function theory (WFT). Associative and dissociative substitution mechanisms were studied, whereby DFT produced inaccurate results for the associative mechanism in contrast to WFT. The Gibbs activation energies (ΔG(‡)) for the dissociative (D) and the associative interchange (Ia) mechanisms, computed with WFT taking into account static and dynamic electron correlation, near-degeneracy, and spin-orbit coupling, are equal within the error limits of the calculations. ΔG(‡) for the water exchange of americyl(VI) via the dissociative mechanism is considerably lower than those for uranyl(VI) and plutonyl(VI) (for which the Ia mechanism is preferred) due to ligand-field effects. On the basis of the present computations, it is not possible to distinguish the Ia from the D mechanism for americyl(VI). In contrast to two other theoretical studies, the dissociative mechanism cannot be ruled out.

  14. Pharmaceutical Applications of Ion-Exchange Resins

    ERIC Educational Resources Information Center

    Elder, David

    2005-01-01

    The historical uses of ion-exchanged resins and a summary of the basic chemical principles involved in the ion-exchanged process are discussed. Specific applications of ion-exchange are provided that include drug stabilization, pharmaceutical excipients, taste-masking agents, oral sustained-release products, topical products for local application…

  15. A Novel Ion Exchange System to Purify Mixed ISS Waste Water Brines for Chemical Production and Enhanced Water Recovery

    NASA Technical Reports Server (NTRS)

    Lunn, Griffin Michael; Spencer, LaShelle E.; Ruby, Anna Maria; McCaskill, Andrew

    2014-01-01

    Current International Space Station water recovery regimes produce a sizable portion of waste water brine. This brine is highly toxic and water recovery is poor: a highly wasteful proposition. With new biological techniques that do not require waste water chemical pretreatment, the resulting brine would be chromium-free and nitrate rich which can allow possible fertilizer recovery for future plant systems. Using a system of ion exchange resins we can remove hardness, sulfate, phosphate and nitrate from these brines to leave only sodium and potassium chloride. At this point modern chlor-alkali cells can be utilized to produce a low salt stream as well as an acid and base stream. The first stream can be used to gain higher water recovery through recycle to the water separation stage while the last two streams can be used to regenerate the ion exchange beds used here, as well as other ion exchange beds in the ISS. Conveniently these waste products from ion exchange regeneration would be suitable as plant fertilizer. In this report we go over the performance of state of the art resins designed for high selectivity of target ions under brine conditions. Using ersatz ISS waste water we can evaluate the performance of specific resins and calculate mass balances to determine resin effectiveness and process viability. If this system is feasible then we will be one step closer to closed loop environmental control and life support systems (ECLSS) for current or future applications.

  16. Ion exchange phenomena

    SciTech Connect

    Bourg, I.C.; Sposito, G.

    2011-05-01

    Ion exchange phenomena involve the population of readily exchangeable ions, the subset of adsorbed solutes that balance the intrinsic surface charge and can be readily replaced by major background electrolyte ions (Sposito, 2008). These phenomena have occupied a central place in soil chemistry research since Way (1850) first showed that potassium uptake by soils resulted in the release of an equal quantity of moles of charge of calcium and magnesium. Ion exchange phenomena are now routinely modeled in studies of soil formation (White et al., 2005), soil reclamation (Kopittke et al., 2006), soil fertilitization (Agbenin and Yakubu, 2006), colloidal dispersion/flocculation (Charlet and Tournassat, 2005), the mechanics of argillaceous media (Gajo and Loret, 2007), aquitard pore water chemistry (Tournassat et al., 2008), and groundwater (Timms and Hendry, 2007; McNab et al., 2009) and contaminant hydrology (Chatterjee et al., 2008; van Oploo et al., 2008; Serrano et al., 2009).

  17. Increasing RO efficiency by chemical-free ion-exchange and Donnan dialysis: Principles and practical implications.

    PubMed

    Vanoppen, Marjolein; Stoffels, Griet; Demuytere, Célestin; Bleyaert, Wouter; Verliefde, Arne R D

    2015-09-01

    Ion-exchange (IEX) and Donnan dialysis (DD) are techniques which can selectively remove cations, limiting scaling in reverse osmosis (RO). If the RO concentrate could be recycled for regeneration of these pre-treatment techniques, RO recovery could be largely increased without the need for chemical addition or additional technologies. In this study, two different RO feed streams (treated industrial waste water and simple tap water) were tested in the envisioned IEX-RO and DD-RO hybrids including RO concentrate recycling. The efficiency of multivalent cation removal depends mainly on the ratio of monovalent to multivalent cations in the feed stream, influencing the ion-exchange efficiency in both IEX and DD. Since the mono-to-multivalent ratio was very high in the waste water, the RO recovery could potentially be increased to 92%. For the tap water, these high RO recoveries could only be reached by adding additional NaCl, because of the low initial monovalent to multivalent ratio in the feed. In both cases, the IEX-RO hybrid proved to be most cost-efficient, due to the high current cost of the membranes used in DD. The membrane cost would have to decrease from ±300 €/m² to 10-30 €/m² - comparable to current reverse osmosis membranes - to achieve a comparable cost. In conclusion, the recycling of RO concentrate to regenerate ion exchange pre-treatment techniques for RO is an interesting option to increase RO recovery without addition of chemicals, but only at high monovalent/multivalent cation-ratios in the feed stream.

  18. Chemical exchange program analysis.

    SciTech Connect

    Waffelaert, Pascale

    2007-09-01

    As part of its EMS, Sandia performs an annual environmental aspects/impacts analysis. The purpose of this analysis is to identify the environmental aspects associated with Sandia's activities, products, and services and the potential environmental impacts associated with those aspects. Division and environmental programs established objectives and targets based on the environmental aspects associated with their operations. In 2007 the most significant aspect identified was Hazardous Materials (Use and Storage). The objective for Hazardous Materials (Use and Storage) was to improve chemical handling, storage, and on-site movement of hazardous materials. One of the targets supporting this objective was to develop an effective chemical exchange program, making a business case for it in FY07, and fully implementing a comprehensive chemical exchange program in FY08. A Chemical Exchange Program (CEP) team was formed to implement this target. The team consists of representatives from the Chemical Information System (CIS), Pollution Prevention (P2), the HWMF, Procurement and the Environmental Management System (EMS). The CEP Team performed benchmarking and conducted a life-cycle analysis of the current management of chemicals at SNL/NM and compared it to Chemical Exchange alternatives. Those alternatives are as follows: (1) Revive the 'Virtual' Chemical Exchange Program; (2) Re-implement a 'Physical' Chemical Exchange Program using a Chemical Information System; and (3) Transition to a Chemical Management Services System. The analysis and benchmarking study shows that the present management of chemicals at SNL/NM is significantly disjointed and a life-cycle or 'Cradle-to-Grave' approach to chemical management is needed. This approach must consider the purchasing and maintenance costs as well as the cost of ultimate disposal of the chemicals and materials. A chemical exchange is needed as a mechanism to re-apply chemicals on site. This will not only reduce the quantity of

  19. Charge exchange molecular ion source

    DOEpatents

    Vella, Michael C.

    2003-06-03

    Ions, particularly molecular ions with multiple dopant nucleons per ion, are produced by charge exchange. An ion source contains a minimum of two regions separated by a physical barrier and utilizes charge exchange to enhance production of a desired ion species. The essential elements are a plasma chamber for production of ions of a first species, a physical separator, and a charge transfer chamber where ions of the first species from the plasma chamber undergo charge exchange or transfer with the reactant atom or molecules to produce ions of a second species. Molecular ions may be produced which are useful for ion implantation.

  20. In-line respeciation: an ion-exchange ion chromatographic method applied to the separation of degradation products of chemical warfare nerve agents in soil.

    PubMed

    Vermillion, W D; Crenshaw, M D

    1997-05-16

    The natural background of anions encountered when analyzing soil samples by ion chromatography (IC) present significant problems in the separation, detection and quantification of isopropyl methylphosphonic acid (IMPA) and methylphosphonic acid (MPA), the degradation products of sarin, a chemical warfare nerve agent. Using chemically-suppressed IC with conductivity detection, a commercially available ion-exchange column, and an isocratic binary eluent system, IMPA and MPA were determined in aqueous extracts of soil at sub-ppm (microgram/g) concentrations without the need for gradient elution or organic solvent eluent modifiers. Common soil anions such as chloride, nitrate, sulfate and phosphate do not interfere with the analysis method due to the composition of the binary eluent allowing for greater mobilization of multivalent anions (e.g., MPA, carbonate, and sulfate) while monovalent anions (e.g., IMPA and nitrate) are relatively unaffected. Carbonate is selectively removed by in-line respeciation to bicarbonate.

  1. Macroreticular chelating ion-exchangers.

    PubMed

    Hirsch, R F; E Gancher, R; Russo, F R

    1970-06-01

    Two macroreticular chelating ion-exchangers have been prepared and characterized. One contains the iminodiacetate group and the second contains the arsonate group as the ion-exchanging site. The macroreticular resins show selectivities among metal ions similar to those of the commercially available naicroreticular chelating resins. Chromatographie separations on the new resins are rapid and sharp.

  2. Ion-exchange hollow fibers

    NASA Technical Reports Server (NTRS)

    Rembaum, Alan (Inventor); Yen, Shiao-Ping S. (Inventor); Klein, Elias (Inventor)

    1977-01-01

    An ion-exchange hollow fiber is prepared by introducing into the wall of the fiber polymerizable liquid monomers, and polymerizing the monomers therein to form solid, insoluble, cross-linked, ion-exchange resin particles which embed in the wall of the fiber. Excess particles blocking the central passage or bore of the fiber are removed by forcing liquid through the fiber. The fibers have high ion-exchange capacity, a practical wall permeability and good mechanical strength even with very thin wall dimensions. Experimental investigation of bundles of ion-exchange hollow fibers attached to a header assembly have shown the fiber to be very efficient in removing counterions from solution.

  3. Ion-exchange hollow fibers

    NASA Technical Reports Server (NTRS)

    Rembaum, Alan (Inventor); Yen, Shiao-Ping S. (Inventor); Klein, Elias (Inventor)

    1980-01-01

    An ion-exchange hollow fiber is prepared by introducing into the wall of the fiber polymerizable liquid monomers, and polymerizing the monomers therein to form solid, insoluble, cross-linked, ion-exchange resin particles which embed in the wall of the fiber. Excess particles blocking the central passage or bore of the fiber are removed by forcing liquid through the fiber. The fibers have high ion-exchange capacity, a practical wall permeability and good mechanical strength even with very thin wall dimensions. Experimental investigation of bundles of ion-exchange hollow fibers attached to a header assembly have shown the fiber to be very efficient in removing counterions from solution.

  4. Ion-exchange hollow fibers

    NASA Technical Reports Server (NTRS)

    Rembaum, A.; Yen, S. P. S.; Klein, E. (Inventor)

    1976-01-01

    An ion-exchange hollow fiber is prepared by introducing into the wall of the fiber polymerizable liquid monomers, and polymerizing the monomers therein to form solid, insoluble, crosslinked, ion-exchange resin particles which embed in the wall of the fiber. Excess particles blocking the central passage or bore of the fiber are removed by forcing liquid through the fiber. The fibers have high ion-exchange capacity, a practical wall permeability and good mechanical strength even with very thin wall dimensions. Experimental investigation of bundles of ion-exchange hollow fibers attached to a header assembly have shown the fiber to be very efficient in removing counterions from solution.

  5. Porous Ceramic Spheres from Ion Exchange Resin

    NASA Technical Reports Server (NTRS)

    Dynys, Fred

    2005-01-01

    A commercial cation ion exchange resin, cross-linked polystyrene, has been successfully used as a template to fabricate 20 to 50 micron porous ceramic spheres. Ion exchange resins have dual template capabilities. Pore architecture of the ceramic spheres can be altered by changing the template pattern. Templating can be achieved by utilizing the internal porous structure or the external surface of the resin beads. Synthesis methods and chemical/physical characteristics of the ceramic spheres will be reported.

  6. Electrically switched ion exchange

    SciTech Connect

    Lilga, M.A.; Schwartz, D.T.; Genders, D.

    1997-10-01

    A variety of waste types containing radioactive {sup 137}Cs are found throughout the DOE complex. These waste types include water in reactor cooling basins, radioactive high-level waste (HLW) in underground storage tanks, and groundwater. Safety and regulatory requirements and economics require the removal of radiocesium before these wastes can be permanently disposed of. Electrically Switched Ion Exchange (ESIX) is an approach for radioactive cesium separation that combines IX and electrochemistry to provide a selective, reversible, and economic separation method that also produces little or no secondary waste. In the ESIX process, an electroactive IX film is deposited electrochemically onto a high-surface area electrode, and ion uptake and elution are controlled directly by modulating the potential of the film. For cesium, the electroactive films under investigation are ferrocyanides, which are well known to have high selectivities for cesium in concentrated sodium solutions. When a cathode potential is applied to the film, Fe{sup +3} is reduced to the Fe{sup +2} state, and a cation must be intercalated into the film to maintain charge neutrality (i.e., Cs{sup +} is loaded). Conversely, if an anodic potential is applied, a cation must be released from the film (i.e., Cs{sup +} is unloaded). Therefore, to load the film with cesium, the film is simply reduced; to unload cesium, the film is oxidized.

  7. Comparison of methods for nutrient measurement in calcareous soils: Ion-exchange resin bag, capsule, membrane, and chemical extractions

    USGS Publications Warehouse

    Sherrod, S.K.; Belnap, J.; Miller, M.E.

    2002-01-01

    Four methods for measuring quantities of 12 plant-available nutrients were compared using three sandy soils in a series of three experiments. Three of the methods use different ion-exchange resin forms-bags, capsules, and membranes-and the fourth was conventional chemical extraction. The first experiment compared nutrient extraction data from a medium of sand saturated with a nutrient solution. The second and third experiments used Nakai and Sheppard series soils from Canyonlands National Park, which are relatively high in soil carbonates. The second experiment compared nutrient extraction data provided by the four methods from soils equilibrated at two temperatures, "warm" and "cold." The third experiment extracted nutrients from the same soils in a field equilibration. Our results show that the four extraction techniques are not comparable. This conclusion is due to differences among the methods in the net quantities of nutrients extracted from equivalent soil volumes, in the proportional representation of nutrients within similar soils and treatments, in the measurement of nutrients that were added in known quantities, and even in the order of nutrients ranked by net abundance. We attribute the disparities in nutrient measurement among the different resin forms to interacting effects of the inherent differences in resin exchange capacity, differences among nutrients in their resin affinities, and possibly the relatively short equilibration time for laboratory trials. One constraint for measuring carbonate-related nutrients in high-carbonate soils is the conventional ammonium acetate extraction method, which we suspect of dissolving fine CaCO3 particles that are more abundant in Nakai series soils, resulting in erroneously high Ca2+ estimates. For study of plant-available nutrients, it is important to identify the nutrients of foremost interest and understand differences in their resin sorption dynamics to determine the most appropriate extraction method.

  8. Ion exchange - Simulation and experiment

    NASA Technical Reports Server (NTRS)

    Herrmann, Cal C.; Finn, John E.

    1991-01-01

    A FORTRAN program for simulating multicomponent adsorption by ion-exchange resins was adapted for use as both an ASPEN-callable module and as a free-standing simulator of the ion-exchange bed. Four polystyrene-divinylbenzene sulfonic acid resins have been characterized for three principal ions. It is concluded that a chelating resin appears appropriate as a heavy-metal trap. The same ASPEN-callable module is used to model this resin when Wilson parameters can be obtained.

  9. Fixation of radioactive ions in porous media with ion exchange gels

    DOEpatents

    Mercer, Jr., Basil W.; Godfrey, Wesley L.

    1979-01-01

    A method is provided for fixing radioactive ions in porous media by injecting into the porous media water-soluble organic monomers which are polymerizable to gel structures with ion exchange sites and polymerizing the monomers to form ion exchange gels. The ions and the particles of the porous media are thereby physically fixed in place by the gel structure and, in addition, the ions are chemically fixed by the ion exchange properties of the resulting gel.

  10. Modeling of Crystalline Silicotitanate Ion Exchange Columns

    SciTech Connect

    Walker, D.D.

    1999-03-09

    Non-elutable ion exchange is being considered as a potential replacement for the In-Tank Precipitation process for removing cesium from Savannah River Site (SRS) radioactive waste. Crystalline silicotitanate (CST) particles are the reference ion exchange medium for the process. A major factor in the construction cost of this process is the size of the ion exchange column required to meet product specifications for decontaminated waste. To validate SRS column sizing calculations, SRS subcontracted two reknowned experts in this field to perform similar calculations: Professor R. G. Anthony, Department of Chemical Engineering, Texas A&038;M University, and Professor S. W. Wang, Department of Chemical Engineering, Purdue University. The appendices of this document contain reports from the two subcontractors. Definition of the design problem came through several meetings and conference calls between the participants and SRS personnel over the past few months. This document summarizes the problem definition and results from the two reports.

  11. Vitrification of ion exchange resins

    DOEpatents

    Cicero-Herman, Connie A.; Workman, Rhonda Jackson

    2001-01-01

    The present invention relates to vitrification of ion exchange resins that have become loaded with hazardous or radioactive wastes, in a way that produces a homogenous and durable waste form and reduces the disposal volume of the resin. The methods of the present invention involve directly adding borosilicate glass formers and an oxidizer to the ion exchange resin and heating the mixture at sufficient temperature to produce homogeneous glass.

  12. Electrically Switched Cesium Ion Exchange

    SciTech Connect

    JPH Sukamto; ML Lilga; RK Orth

    1998-10-23

    This report discusses the results of work to develop Electrically Switched Ion Exchange (ESIX) for separations of ions from waste streams relevant to DOE site clean-up. ESIX combines ion exchange and electrochemistry to provide a selective, reversible method for radionuclide separation that lowers costs and minimizes secondary waste generation typically associated with conventional ion exchange. In the ESIX process, an electroactive ion exchange film is deposited onto. a high surface area electrode, and ion uptake and elution are controlled directly by modulating the potential of the film. As a result, the production of secondary waste is minimized, since the large volumes of solution associated with elution, wash, and regeneration cycles typical of standard ion exchange are not needed for the ESIX process. The document is presented in two parts: Part I, the Summary Report, discusses the objectives of the project, describes the ESIX concept and the approach taken, and summarizes the major results; Part II, the Technology Description, provides a technical description of the experimental procedures and in-depth discussions on modeling, case studies, and cost comparisons between ESIX and currently used technologies.

  13. Ion exchange tempering of glass ophthalmic lenses.

    PubMed

    Keeney, A H; Duerson, H L

    1975-08-01

    We performed low velocity drop-ball tests using 5/8-, 7/8-, and 1-inch diameter steel balls on ophthalmic crown glass lenses chemically tempered by the ion exchange process. Four representative dioptric strengths (+ 2.50 spherical, - 2.50 spherical, -2.50 cylindrical, and plano) were studied with the isolated lenses mounted, convex side up, on the American National Standards Institute Z80 test block. New ion exchange lenses exhibited a 100 to 350% greater capacity for attenuation of energy from low velocity, large size missiles than matched lenses of similar strength prepared by the conventional heat-treating and air-quenching process.

  14. The role of metal ions in chemical evolution - Polymerization of alanine and glycine in a cation-exchanged clay environment

    NASA Technical Reports Server (NTRS)

    Lawless, J. G.; Levi, N.

    1979-01-01

    The effect of the exchangeable cation on the condensation of glycine and alanine was investigated using a series of homoionic bentonites. A cycling procedure of drying, warming and wetting was employed. Peptide bond formation was observed, and the effectiveness of metal ions to catalyze the condensation was Cu(2+) greater than Ni(2) approximately equals Zn(2+) greater than Na(+). Glycine showed 6% of the monomer incorporated into oligomers with the largest detected being the pentamer. Alanine showed less peptide bond formation (a maximum of 2%) and only the dimer was observed.

  15. Ion-pairing dynamics of Li{sup +} and SCN{sup -} in dimethylformamide solution: Chemical exchange two-dimensional infrared spectroscopy

    SciTech Connect

    Lee, Kyung-Koo; Park, Kwang-Hee; Kwon, Donghyun; Choi, Jun-Ho; Son, Hyewon; Park, Sungnam; Cho, Minhaeng

    2011-02-14

    Ultrafast two-dimensional infrared (2DIR) spectroscopy has been proven to be an exceptionally useful method to study chemical exchange processes between different vibrational chromophores under thermal equilibria. Here, we present experimental results on the thermal equilibrium ion pairing dynamics of Li{sup +} and SCN{sup -} ions in N,N-dimethylformamide. Li{sup +} and SCN{sup -} ions can form a contact ion pair (CIP). Varying the relative concentration of Li{sup +} in solution, we could control the equilibrium CIP and free SCN{sup -} concentrations. Since the CN stretch frequency of Li-SCN CIP is blue-shifted by about 16 cm{sup -1} from that of free SCN{sup -} ion, the CN stretch IR spectrum is a doublet. The temperature-dependent IR absorption spectra reveal that the CIP formation is an endothermic (0.57 kJ/mol) process and the CIP state has larger entropy by 3.12 J/(K mol) than the free ion states. Since the two ionic configurations are spectrally distinguishable, this salt solution is ideally suited for nonlinear IR spectroscopic investigations to study ion pair association and dissociation dynamics. Using polarization-controlled IR pump-probe methods, we first measured the lifetimes and orientational relaxation times of these two forms of ionic configurations. The vibrational population relaxation times of both the free ion and CIP are about 32 ps. However, the orientational relaxation time of the CIP, which is {approx}47 ps, is significantly longer than that of the free SCN{sup -}, which is {approx}7.7 ps. This clearly indicates that the effective moment of inertia of the CIP is much larger than that of the free SCN{sup -}. Then, using chemical exchange 2DIR spectroscopy and analyzing the diagonal peak and cross-peak amplitude changes with increasing the waiting time, we determined the contact ion pair association and dissociation time constants that are found to be 165 and 190 ps, respectively. The results presented and discussed in this paper are believed

  16. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E. Philip; Alexandratos, Spiro D.; Gatrone, Ralph C.; Chiarizia, Ronato

    1996-01-01

    An ion exchange resin for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene diphosphonic acid with styrene, acrylonitrile and divinylbenzene.

  17. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E. Philip; Alexandratos, Spiro D.; Gatrone, Ralph C.; Chiarizia, Ronato

    1994-01-01

    An ion exchange resin for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene disphosphonic acid with styrene, acrylonitrile and divinylbenzene.

  18. Ion exchange of cesium by crystalline silico-titanates

    SciTech Connect

    Zheng, Zhixin; Anthony, R.G.; Miller, J.E.; Trudell, D.

    1995-12-01

    The crystalline silico-titanates developed by the Department of Chemical Engineering at Texas A&M University, Sandia National Laboratories and UOP exhibits extremely high ion exchange selectivity for removing cesium from aqueous defense wastes. Based on experimental data and structure studies, a competitive ion exchange model was proposed to predict the ion exchange performance in different simulated waste solutions. The predicted distribution coefficients were within 10% of the experimentally determined values.

  19. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, A.W.; Gatrone, R.C.; Alexandratos, S.; Horwitz, E.P.

    1997-04-08

    An ion exchange resin is disclosed that is comprised of an insoluble copolymer onto which are grafted pendent groups that provide 1.0 to about 10 mmol/g dry weight phosphorus. The pendent groups have the formula as shown in the patent wherein R is hydrogen, a cation or mixtures thereof; and R{sup 1} is hydrogen or an C{sub 1}-C{sub 2} alkyl group. The resin also contains zero to about 5 mmol/g dry weight of pendent aromatic sulfonate groups. Processes for making and using an ion exchange resin are also disclosed.

  20. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, Andrzej W.; Gatrone, Ralph C.; Alexandratos, Spiro; Horwitz, E. Philip

    1998-01-27

    An ion exchange resin is disclosed that is comprised of an insoluble copolymer onto which are grafted pendent groups that provide 1.0 to about 10 mmol/g dry weight phosphorous. The pendent groups have the formula ##STR1## wherein R is hydrogen, a cation or mixtures thereof; and R.sup.1 is hydrogen or an C.sub.1 -C.sub.2 alkyl group. The resin also contains zero to about 5 mmol/g dry weight of pendent aromatic sulfonate groups. Processes for making and using an ion exchange-resin are also disclosed.

  1. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, Andrzej W.; Gatrone, Ralph C.; Alexandratos, Spiro; Horwitz, E. Philip

    1997-01-01

    An ion exchange resin is disclosed that is comprised of an insoluble copolymer onto which are grafted pendent groups that provide 1.0 to about 10 mmol/g dry weight phosphorous. The pendent groups have the formula ##STR1## wherein R is hydrogen, a cation or mixtures thereof; and R.sup.1 is hydrogen or an C.sub.1 -C.sub.2 alkyl group. The resin also contains zero to about 5 mmol/g dry weight of pendent aromatic sulfonate groups. Processes for making and using an ion exchange resin are also disclosed.

  2. Radiation Studies with Argentine Ion Exchange Material

    SciTech Connect

    Crawford, C.L.

    2002-06-28

    A recent technology exchange between Argentina Nuclear Energy Commission (CNEA) and the US Department of Energy involved vitrification studies of ion exchange resins. Details of the spent ion exchange resins currently stored at two Argentine nuclear power plants, Atucha I and Embalse, have been presented in earlier reports. The present study examines irradiation of simulant samples of ion exchange resins.

  3. Ion Exchange and Liquid Column Chromatography.

    ERIC Educational Resources Information Center

    Walton, Harold F.

    1980-01-01

    Emphasizes recent advances in principles and methodology in ion exchange and chromatography. Two tables list representative examples for inorganic ions and organic compounds. Cites 544 references. (CS)

  4. Chemical and radiation stability of SuperLig{reg_sign}644, resorcinol-formaldehyde, and CS-100 cesium ion exchange materials

    SciTech Connect

    Brown, G.N.; Adami, S.R.; Bray, L.A.

    1995-09-01

    At the request of the Initial Pretreatment Module Project within Westinghouse Hanford Company, Pacific Northwest Laboratory (PNL) conducted this study for the Efficient Separations and Processing Crosscutting Program (ESP) under the task ``Develop and Test Sorbents.`` The purpose of the study was to assess and compare the chemical and radiolytic stability of several cesium-selective ion exchange materials in simulated alkaline Hanford tank waste matrices. Pretreatment of nuclear process wastes to remove of cesium and other radionuclides by ion exchange was proposed previously as one method of minimizing the amount of high-level radioactive waste at Hanford. In this study, PNL evaluated three cesium-selective materials SuperLig{reg_sign}644, resorcinol-formaldehyde (R-F), and CS-100 for chemical and radiation stability in 1 M NaOH and a simulated neutralized current acid waste (NCAW). The objective of the study is to investigate the stability of the newly produced SuperLig{reg_sign}644 under a variety of conditions in an attempt to simulate and predict the degradation process. The following specific conclusions and recommendations resulted from the study.

  5. Ion exchange purification of scandium

    DOEpatents

    Herchenroeder, Laurie A.; Burkholder, Harvey R.

    1990-10-23

    An improvement in purification of scandium through ion exchange chromatography is disclosed in which the oxidation potential of the eluting solution is altered by the addition of potassium chlorate or ammonium chloride so that removal of contaminants is encouraged. The temperature, pH and concentration of the eluent HEDTA are controlled in order to maintain the scandium in the column while minimizing dilution of the scandium band. Recovery of scandium is improved by pumping dilute scandium over the column prior to stripping the scandium and precipitation. This eliminates the HEDTA ion and other monovalent cations contaminating the scandium band. This method maximizes recovery of scandium while maintaining purity.

  6. Ion exchange purification of scandium

    DOEpatents

    Herchenroeder, L.A.; Burkholder, H.R.

    1990-10-23

    An improvement in purification of scandium through ion exchange chromatography is disclosed in which the oxidation potential of the eluting solution is altered by the addition of potassium chlorate or ammonium chloride so that removal of contaminants is encouraged. The temperature, pH and concentration of the eluent HEDTA are controlled in order to maintain the scandium in the column while minimizing dilution of the scandium band. Recovery of scandium is improved by pumping dilute scandium over the column prior to stripping the scandium and precipitation. This eliminates the HEDTA ion and other monovalent cations contaminating the scandium band. This method maximizes recovery of scandium while maintaining purity. 2 figs.

  7. Electrically controlled cesium ion exchange

    SciTech Connect

    Lilga, M.

    1996-10-01

    Several sites within the DOE complex (Savannah River, Idaho, Oak Ridge and Hanford) have underground storage tanks containing high-level waste resulting from nuclear engineering activities. To facilitate final disposal of the tank waste, it is advantageous to separate and concentrate the radionuclides for final immobilization in a vitrified glass matrix. This task proposes a new approach for radionuclide separation by combining ion exchange (IX) and electrochemistry to provide a selective and economic separation method.

  8. Effect of resin charged functional group, porosity, and chemical matrix on the long-term pharmaceutical removal mechanism by conventional ion exchange resins.

    PubMed

    Wang, Wei; Li, Xiaofeng; Yuan, Shengliu; Sun, Jian; Zheng, Shaokui

    2016-10-01

    This study attempted to clarify the long-term pharmaceutical removal mechanism from sewage treatment plant effluent during the cyclical adsorption-regeneration operation of 5 commercial resin-based fixed-bed reactors with the simultaneous occurrence of electrostatic interactions and complex non-electrostatic interactions. It examined 12 pharmaceuticals belonging to 10 therapeutic classes with different predominant existing forms and hydrophobicities. Furthermore, the effect of the resin charged functional group (strong-base vs. strong-acid vs. non-ionic), porosity (macroporous vs. gel), and chemical matrix (polystyrenic vs. polyacrylic) on the mechanism was investigated to optimize resin properties and achieve higher pharmaceutical removal. The results reported herein indicate the importance of non-electrostatic interactions between pharmaceuticals and the resin backbone during short-term cyclical operation (i.e., the 1st adsorption-regeneration cycle). With the development of cyclical operation, however, non-electrostatic interaction-induced pharmaceutical removal generally decreased and even disappeared when equilibrium was achieved between the influent and the resin. Despite pharmaceutical therapeutic class or hydrophilicity, anion (or cation) exchange resin preferentially removed those pharmaceuticals that were predominantly present as organic anions (or cations) by ion exchange process during long-term cyclical operation (i.e., ≥6 adsorption-regeneration cycles). Besides pharmaceuticals predominantly present as undissociated molecules, some amphoteric pharmaceuticals containing large amounts of zwitterions were also difficult to remove by ion exchange resin. Additionally, neither resin porosity nor chemical matrix had any significant effect on the long-term pharmaceutical removal mechanism.

  9. Synthesis and ion-exchange properties of lanthanum tungstate, a new inorganic ion exchanger

    SciTech Connect

    Husain, S.W.; Rasheedzad, S.; Manzoori, J.L.; Jabbari, Y.

    1982-01-01

    Amorphous samples of a new inorganic ion exchanger, lanthanum tungstate, have been prepared under varying conditions. The material prepared by mixing 0.05 M lanthanum nitrate and 0.05 M sodium tungstate in a ratio of 1:2 was studied in detail for its ion-exchange capacity, chemical stability, ir, thermogravimetry, and K/sub d/ values. Its columns have been used for the separation of C/sup 2 +/ from Pd/sup 2 +/, Mn/sup 2 +/, and Cu/sup 2 +/, and Ni/sup 2 +/ from Pd/sup 2 +/. 3 figures, 4 tables.

  10. Ion exchange materials, method of forming ion exchange materials, and methods of treating liquids

    DOEpatents

    Wertsching, Alan K.; Peterson, Eric S.; Wey, John E.

    2007-12-25

    The invention includes an ion affinity material having an organic component which is sulfonated and which is chemically bonded to an inorganic substrate component. The invention includes a method of forming a metal binding material. A solid support material comprising surface oxide groups is provided and an organic component having at least one alkyl halide is covalently linked to at least some of the surface oxide groups to form a modified support material. The at least one alkyl halide is subsequently converted into an alkyl sulfonate. The invention further includes a method and system for extracting ions from a liquid. An ion exchange material having a sulfonated alkyl silane component covalently bonded to a metal oxide support material is provided and a liquid is exposed to the ion exchange material.

  11. Using Ion Exchange Chromatography to Separate and Quantify Complex Ions

    ERIC Educational Resources Information Center

    Johnson, Brian J.

    2014-01-01

    Ion exchange chromatography is an important technique in the separation of charged species, particularly in biological, inorganic, and environmental samples. In this experiment, students are supplied with a mixture of two substitution-inert complex ions. They separate the complexes by ion exchange chromatography using a "flash"…

  12. Ion Exchange Formation via Sulfonated Bicomponent Nonwovens

    NASA Astrophysics Data System (ADS)

    Stoughton, Hannah L.

    For many years ion exchange resins were used to: remove heavy metals from water, recover materials from wastewater, and eliminate harmful gases from the air. While use of these resin beads dominates the ion exchange industry, the beads have limitations that should be considered when decisions are made to employ them. For instance, officials must balance the inherent zero sum surface area and porosity of the materials. This series of studies investigates the use of bicomponent nonwovens as a base substrate for producing high surface area ion exchange materials for the removal of heavy metal ions. Functionalized materials were produced in a two-step process: (1) PET/PE spunbond bicomponent fibers were fractured completely, producing the high surface area nonwoven to be used as the base ion exchange material, and (2) the conditions for functionalizing the PET fibers of the nonwoven webs were investigated where an epoxy containing monomer was grafted to the surface followed by sulfonation of the monomer. The functionalization reactions of the PET fibers were monitored based on: weight gain, FTIR, TOF-SIMS, and SEM. Ion exchange properties were evaluated using titration and copper ion removal capacity from test solutions. The relationship between web structure and removal efficiency of the metal ions was defined through a comparison of the bicomponent and homocomponent nonwovens for copper ion removal efficiency. The investigation revealed that utilizing the high surface area, fractured bicomponent nonwoven ion exchange materials with capacities comparable to commercially available ion exchange resins could be produced.

  13. Ion-exchange chromatographic protein refolding.

    PubMed

    Freydell, Esteban J; van der Wielen, Luuk; Eppink, Michel; Ottens, Marcel

    2010-11-12

    The application of ion-exchange (IEX) chromatography to protein refolding (IExR) has been successfully proven, as supported by various studies using different model proteins, ion-exchange media and flow configurations. Ion-exchange refolding offers a relatively high degree of process intensification, represented by the possibility of performing protein refolding, product purification and product concentration, in one unit operation. Besides its high degree of process intensification, IExR offers an additional set of key advantages including: spatial isolation of the bound protein molecules and the controllable change in chemical composition using gradients. Despite of the acknowledgement of the former advantages, the lack of mechanistic understanding on how they influence the process performance of the ion-exchange refolding reactor, limits the ability to exploit them in order to optimize the performance of the unit. This paper presents a quantitative analysis that assesses the effect that the spatial isolation and the urea gradient, have on the IExR performance, judged on the basis of the refolding yield (Y(N)) and the fractional mass recovery (f(Prot,Rec)). Additionally, this work discusses the effect of the protein load, the protein loading state (i.e., native, denatured, denatured and reduced (D&R)) and the adsorbent type on f(Prot,Rec). The presented work shows: (1) that the protein load has a direct effect on f(Prot,Rec), and the magnitude of this effect depends on the loading state of the protein solution and the adsorbent type; (2) that irrespectively of the type of adsorbent used, the saturation capacity of a denatured protein is less than the native protein and that this difference can be linked to differences in accessible binding surface area; (3) that there is a clear correlation between fractional surface coverage (θ) and f(Prot,Rec), indicating that the former could serve as a good descriptor to assess spatial isolation, and (4) that the urea

  14. [Ion specificity during ion exchange equilibrium in natural clinoptilolite].

    PubMed

    He, Yun-Hua; Li, Hang; Liu, Xin-Min; Xiong, Hai-Ling

    2015-03-01

    Zeolites have been widely applied in soil improvement and environment protection. The study on ion specificity during ion exchange equilibrium is of important significance for better use of zeolites. The maximum adsorption capacities of alkali ions during ion exchange equilibrium in the clinoptilolite showed obvious specificity. For alkali metal ions with equivalent valence, the differences in adsorption capacity increased with the decrease of ionic concentration. These results cannot be well explained by the classical theories including coulomb force, ionic size, hydration, dispersion force, classic induction force and surface complexation. We found that the coupling of polarization effects resulted from the quantum fluctuation of diverse alkali metal ions and electric field near the zeolite surface should be the primary reason for specific ion effect during ion exchange in zeolite. The result of this coupling effect was that the difference in the ion dipole moment increased with the increase of surface potential, which further expanded the difference in the adsorption ability between zeolite surface and ions, resulting in different ion exchange adsorption ability at the solid/liquid interface. Due to the high surface charge density of zeolite, ionic size also played an important role in the distribution of ions in the double diffuse layer, which led to an interesting result that distinct differences in exchange adsorption ability of various alkali metal ions were only detected at high surface potential (the absolute value was greater than 0.2 V), which was different from the ion exchange equilibrium result on the surface with low charge density.

  15. Ion exchange defines the biological activity of titanate nanotubes.

    PubMed

    Rónavári, Andrea; Kovács, Dávid; Vágvölgyi, Csaba; Kónya, Zoltán; Kiricsi, Mónika; Pfeiffer, Ilona

    2016-05-01

    One-dimensional titanate nanotubes (TiONTs) were subjected to systematic ion exchange to determine the impact of these modifications on biological activities. Ion exchanged TiONTs (with Ag, Mg, Bi, Sb, Ca, K, Sr, Fe, and Cu ions) were successfully synthesized and the presence of the substituted ions was verified by energy dispersive X-ray spectroscopy (EDS). A complex screening was carried out to reveal differences in toxicity to human cells, as well as in antibacterial, antifungal, and antiviral activities between the various modified nanotubes. Our results demonstrated that Ag ion exchanged TiONTs exerted potent antibacterial and antifungal effects against all examined microbial species but were ineffective on viruses. Surprisingly, the antibacterial activity of Cu/TiONTs was restricted to Micrococcus luteus. Most ion exchanged TiONTs did not show antimicrobial activity against the tested bacterial and fungal species. Incorporation of various ions into nanotube architectures lead to mild, moderate, or even to a massive loss of human cell viability; therefore, this type of biological effect exerted by TiONTs can be greatly modulated by ion exchange. These findings further emphasize the contribution of ion exchange in determining not only the physical and chemical characteristics but also the bioactivity of TiONT against different types of living cells.

  16. Ion exchange in the nuclear industry

    SciTech Connect

    Bibler, J.P.

    1990-01-01

    Ion exchange is used in nearly every part of the nuclear fuel cycle -- from the purification of uranium from its ore to the final recovery of uranium and transmutation products. Ion exchange also plays a valuable role in the management of nuclear wastes generated in the fuel cycle.

  17. Ion exchange in the nuclear industry

    SciTech Connect

    Bibler, J.P.

    1990-12-31

    Ion exchange is used in nearly every part of the nuclear fuel cycle -- from the purification of uranium from its ore to the final recovery of uranium and transmutation products. Ion exchange also plays a valuable role in the management of nuclear wastes generated in the fuel cycle.

  18. Titania bound sodium titanate ion exchanger

    DOEpatents

    DeFilippi, Irene C. G.; Yates, Stephen Frederic; Shen, Jian-Kun; Gaita, Romulus; Sedath, Robert Henry; Seminara, Gary Joseph; Straszewski, Michael Peter; Anderson, David Joseph

    1999-03-23

    This invention is method for preparing a titania bound ion exchange composition comprising admixing crystalline sodium titanate and a hydrolyzable titanium compound and, thereafter drying the titania bound crystalline sodium titanate and subjecting the dried titania bound ion exchange composition to optional compaction and calcination steps to improve the physical strength of the titania bound composition.

  19. Ion Exchange and Adsorption of Inorganic Contaminants

    EPA Science Inventory

    In the first part of the chapter, the fundamentals of ion exchange and adsorption processes are explained, with the goal of demonstrating how these principles influence process design for inorganic contaminant removal. In the second part, ion exchange and adsorption processes th...

  20. Ion Exchange Membrane Influence on Ohmic Resistance

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Selection of the proper ion exchange membrane can have a significant influence on bioelectrochemical system (BES) power densities. Because ions move across the membrane to achieve electroneutrality, the ion transport resistance (ohmic loss) needs to be minimized to increase power densities. Ohmic ...

  1. Closed cycle ion exchange method for regenerating acids, bases and salts

    DOEpatents

    Dreyfuss, Robert M.

    1976-01-01

    A method for conducting a chemical reaction in acidic, basic, or neutral solution as required and then regenerating the acid, base, or salt by means of ion exchange in a closed cycle reaction sequence which comprises contacting the spent acid, base, or salt with an ion exchanger, preferably a synthetic organic ion-exchange resin, so selected that the counter ions thereof are ions also produced as a by-product in the closed reaction cycle, and then regenerating the spent ion exchanger by contact with the by-product counter ions. The method is particularly applicable to closed cycle processes for the thermochemical production of hydrogen.

  2. Ibuprofen ion-exchange fiber complex: improved dissolution and gastric tolerance based on ion exchange.

    PubMed

    Che, Xin; Wang, Li-hong; Yang, Yang; Yuan, Yue; Wang, Qi-fang; Wang, Yan; Li, San-ming

    2013-05-01

    The purpose of the present study is to develop a novel method to improve the dissolution of water-insoluble drug ibuprofen and the gastric tolerance of this non-steroidal anti-inflammatory drug which has potentially serious gastrointestinal side effects. This method is based on ion exchange of ion-exchange fibers. Water-insoluble drug ibuprofen was dispersed in deionized water, and then the ion-exchange fibers in OH(-) type was immersed in it. Ibuprofen and the active groups of the ion-exchange fibers combined into ion pairs based on the acid-base reaction. This drug carrier did not release drugs in deionized water, but in water solution containing other ions it would release the drugs into the solution by ion exchange. Confirmed by the X-ray diffraction and the scanning electron microscopy, the ibuprofen combined onto the ion-exchange fibers was in a highly molecular level dispersed state. The improved dissolution of ibuprofen ion-exchange fiber complexes is likely to originate from this ibuprofen's highly dispersed state. Due to this, ibuprofen's highly dispersed state, ibuprofen ion-exchange fiber complexes significantly decreases the gastrointestinal side effects of ibuprofen by avoiding the solid ibuprofen's educing. The present study showed that ibuprofen ion-exchange fiber complexes have the two-fold advantages. One is to improve the dissolution of ibuprofen. The other is to decrease the ibuprofen's gastrointestinal toxicity.

  3. Ion Exchange in Glass-Ceramics

    NASA Astrophysics Data System (ADS)

    Beall, George; Comte, Monique; Deneka, Matthew; Marques, Paulo; Pradeau, Philippe; Smith, Charlene

    2016-08-01

    In the past few years ion-exchange in glasses has found a renewed interest with a lot of new development and research in industrial and academic labs and the commercialization of materials with outstanding mechanical properties. These glasses are now widely used in many electronic devices including hand-held displays and tablets. The exchange is generally conducted in a bath of molten salt below the transition temperature of the glass. The exchange at the surface of an alkali ion by a bigger one brings compressive stress at the surface. The mechanical properties are dependent on the stress level at the surface and the depth of penetration of the bigger ion. As compared to glasses, glass-ceramics have the interest to display a wide range of aspects (transparent to opaque) and different mechanical properties (especially higher modulus and toughness). There has been little research on ion-exchange in glass-ceramics. In these materials the mechanisms are much more complex than in glasses because of their polyphasic nature: ion-exchange generally takes place mostly in one phase (crystalline phase or residual glass). The mechanism can be similar to what is observed in glasses with the replacement of an ion by another in the structure. But in some cases this ion-exchange leads to microstructural modifications (for example amorphisation or phase change). This article reviews these ion-exchange mechanisms using several transparent and opaque alumino-silicate glass-ceramics as examples. The effect of the ion exchange in the various glass-ceramics will be described, with particular emphasis on flexural strength.

  4. Ultrafast two dimensional infrared chemical exchange spectroscopy

    NASA Astrophysics Data System (ADS)

    Fayer, Michael

    2011-03-01

    The method of ultrafast two dimensional infrared (2D IR) vibrational echo spectroscopy is described. Three ultrashort IR pulses tuned to the frequencies of the vibrational transitions of interest are directed into the sample. The interaction of these pulses with the molecular vibrational oscillators produces a polarization that gives rise to a fourth pulse, the vibrational echo. The vibrational echo pulse is combined with another pulse, the local oscillator, for heterodyne detection of the signal. For fixed time between the second and third pulses, the waiting time, the first pulse is scanned. Two Fourier transforms of the data yield a 2D IR spectrum. The waiting time is increased, and another spectrum is obtained. The change in the 2D IR spectra with increased waiting time provides information on the time evolution of the structure of the molecular system under observation. In a 2D IR chemical exchange experiment, two species A and B, are undergoing chemical exchange. A's are turning into B's, and B's are turning into A's, but the overall concentrations of the species are not changing. The kinetics of the chemical exchange on the ground electronic state under thermal equilibrium conditions can be obtained 2D IR spectroscopy. A vibration that has a different frequency for the two species is monitored. At very short time, there will be two peaks on the diagonal of the 2D IR spectrum, one for A and one for B. As the waiting time is increased, chemical exchange causes off-diagonal peaks to grow in. The time dependence of the growth of these off-diagonal peaks gives the chemical exchange rate. The method is applied to organic solute-solvent complex formation, orientational isomerization about a carbon-carbon single bond, migration of a hydrogen bond from one position on a molecule to another, protein structural substate interconversion, and water hydrogen bond switching between ions and water molecules. This work was supported by the Air Force Office of Scientific

  5. MODELING RESULTS FROM CESIUM ION EXCHANGE PROCESSING WITH SPHERICAL RESINS

    SciTech Connect

    Nash, C.; Hang, T.; Aleman, S.

    2011-01-03

    Ion exchange modeling was conducted at the Savannah River National Laboratory to compare the performance of two organic resins in support of Small Column Ion Exchange (SCIX). In-tank ion exchange (IX) columns are being considered for cesium removal at Hanford and the Savannah River Site (SRS). The spherical forms of resorcinol formaldehyde ion exchange resin (sRF) as well as a hypothetical spherical SuperLig{reg_sign} 644 (SL644) are evaluated for decontamination of dissolved saltcake wastes (supernates). Both SuperLig{reg_sign} and resorcinol formaldehyde resin beds can exhibit hydraulic problems in their granular (nonspherical) forms. SRS waste is generally lower in potassium and organic components than Hanford waste. Using VERSE-LC Version 7.8 along with the cesium Freundlich/Langmuir isotherms to simulate the waste decontamination in ion exchange columns, spherical SL644 was found to reduce column cycling by 50% for high-potassium supernates, but sRF performed equally well for the lowest-potassium feeds. Reduced cycling results in reduction of nitric acid (resin elution) and sodium addition (resin regeneration), therefore, significantly reducing life-cycle operational costs. These findings motivate the development of a spherical form of SL644. This work demonstrates the versatility of the ion exchange modeling to study the effects of resin characteristics on processing cycles, rates, and cold chemical consumption. The value of a resin with increased selectivity for cesium over potassium can be assessed for further development.

  6. ION EXCHANGE PERFORMANCE OF TITANOSILICATES, GERMANATES AND CARBON NANOTUBES

    SciTech Connect

    Alsobrook, A. N.; Hobbs, D. T.

    2013-04-24

    This report presents a summary of testing the affinity of titanosilicates (TSP), germanium-substituted titanosilicates (Ge-TSP) and multiwall carbon nanotubes (MWCNT) for lanthanide ions in dilute nitric acid solution. The K-TSP ion exchanger exhibited the highest affinity for lanthanides in dilute nitric acid solutions. The Ge-TSP ion exchanger shows promise as a material with high affinity, but additional tests are needed to confirm the preliminary results. The MWCNT exhibited much lower affinities than the K-TSP in dilute nitric acid solutions. However, the MWCNT are much more chemically stable to concentrated nitric acid solutions and, therefore, may candidates for ion exchange in more concentrated nitric acid solutions. This technical report serves as the deliverable documenting completion of the FY13 research milestone, M4FT-13SR0303061 – measure actinide and lanthanide distribution values in nitric acid solutions with sodium and potassium titanosilicate materials.

  7. Ion exchanges in apatites for biomedical application.

    PubMed

    Cazalbou, S; Eichert, D; Ranz, X; Drouet, C; Combes, C; Harmand, M F; Rey, C

    2005-05-01

    The modification of the composition of apatite materials can be made by several processes corresponding to ion exchange reactions which can conveniently be adapted to current coatings and ceramics and are an alternative to setting up of new synthesis methods. In addition to high temperature thermal treatments, which can partly or almost totally replace the monovalent OH- anion of stoichiometric hydroxyapatite by any halogen ion or carbonate, aqueous processes corresponding to dissolution-reprecipitation reactions have also been proposed and used. However, the most interesting possibilities are provided by aqueous ion exchange reactions involving nanocrystalline apatites. These apatites are characterised by the existence on the crystal surface of a hydrated layer of loosely bound mineral ions which can be easily exchanged in solution. This layer offers a possibility to trap mineral ions and possibly active molecules which can modify the apatite properties. Such processes are involved in mineralised tissues and could be used in biomaterials for the release of active mineral species.

  8. ION EXCHANGE SOFTENING: EFFECTS ON METAL CONCENTRATIONS

    EPA Science Inventory

    A corrosion control pipe loop study to evaluate the effect of ion exchange water softening on metal leaching from household plumbing materials was conducted on two different water qualities having different pH's and hardness levels. The results showed that removing hardness ions ...

  9. Inorganic ion exchangers for nuclear waste remediation

    SciTech Connect

    Clearfield, A.; Bortun, A.; Bortun, L.; Behrens, E.

    1997-10-01

    The objective of this work is to provide a broad spectrum of inorganic ion exchangers that can be used for a range of applications and separations involving remediation of groundwater and tank wastes. The authors intend to scale-up the most promising exchangers, through partnership with AlliedSignal Inc., to provide samples for testing at various DOE sites. While much of the focus is on exchangers for removal of Cs{sup +} and Sr{sup 2+} from highly alkaline tank wastes, especially at Hanford, the authors have also synthesized exchangers for acid wastes, alkaline wastes, groundwater, and mercury, cobalt, and chromium removal. These exchangers are now available for use at DOE sites. Many of the ion exchangers described here are new, and others are improved versions of previously known exchangers. They are generally one of three types: (1) layered compounds, (2) framework or tunnel compounds, and (3) amorphous exchangers in which a gel exchanger is used to bind a fine powder into a bead for column use. Most of these exchangers can be regenerated and used again.

  10. 21 CFR 173.20 - Ion-exchange membranes.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ion-exchange membranes. 173.20 Section 173.20 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.20 Ion-exchange membranes. Ion-exchange... ion-exchange membrane is prepared by subjecting a polyethylene base conforming to § 177.1520 of...

  11. 21 CFR 173.20 - Ion-exchange membranes.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ion-exchange membranes. 173.20 Section 173.20 Food... for Food Treatment § 173.20 Ion-exchange membranes. Ion-exchange membranes may be safely used in the processing of food under the following prescribed conditions: (a) The ion-exchange membrane is prepared...

  12. 21 CFR 173.20 - Ion-exchange membranes.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ion-exchange membranes. 173.20 Section 173.20 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.20 Ion-exchange membranes. Ion-exchange... ion-exchange membrane is prepared by subjecting a polyethylene base conforming to § 177.1520 of...

  13. 21 CFR 173.20 - Ion-exchange membranes.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ion-exchange membranes. 173.20 Section 173.20 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.20 Ion-exchange membranes. Ion-exchange... ion-exchange membrane is prepared by subjecting a polyethylene base conforming to § 177.1520 of...

  14. 21 CFR 173.20 - Ion-exchange membranes.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ion-exchange membranes. 173.20 Section 173.20 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.20 Ion-exchange membranes. Ion-exchange... ion-exchange membrane is prepared by subjecting a polyethylene base conforming to § 177.1520 of...

  15. Heat Exchanger Lab for Chemical Engineering Undergraduates

    ERIC Educational Resources Information Center

    Rajala, Jonathan W.; Evans, Edward A.; Chase, George G.

    2015-01-01

    Third year chemical engineering undergraduate students at The University of Akron designed and fabricated a heat exchanger for a stirred tank as part of a Chemical Engineering Laboratory course. The heat exchanger portion of this course was three weeks of the fifteen week long semester. Students applied concepts of scale-up and dimensional…

  16. MINOR ACTINIDE SEPARATIONS USING ION EXCHANGERS OR IONIC LIQUIDS

    SciTech Connect

    Hobbs, D.; Visser, A.; Bridges, N.

    2011-09-20

    This project seeks to determine if (1) inorganic-based ion exchange materials or (2) electrochemical methods in ionic liquids can be exploited to provide effective Am and Cm separations. Specifically, we seek to understand the fundamental structural and chemical factors responsible for the selectivity of inorganic-based ion-exchange materials for actinide and lanthanide ions. Furthermore, we seek to determine whether ionic liquids can serve as the electrolyte that would enable formation of higher oxidation states of Am and other actinides. Experiments indicated that pH, presence of complexants and Am oxidation state exhibit significant influence on the uptake of actinides and lanthanides by layered sodium titanate and hybrid zirconium and tin phosphonate ion exchangers. The affinity of the ion exchangers increased with increasing pH. Greater selectivity among Ln(III) ions with sodium titanate materials occurs at a pH close to the isoelectric potential of the ion exchanger. The addition of DTPA decreased uptake of Am and Ln, whereas the addition of TPEN generally increases uptake of Am and Ln ions by sodium titanate. Testing confirmed two different methods for producing Am(IV) by oxidation of Am(III) in ionic liquids (ILs). Experimental results suggest that the unique coordination environment of ionic liquids inhibits the direct electrochemical oxidation of Am(III). The non-coordinating environment increases the oxidation potential to a higher value, while making it difficult to remove the inner coordination of water. Both confirmed cases of Am(IV) were from the in-situ formation of strong chemical oxidizers.

  17. Effect of polyamine reagents on exchange capacity in ion exchangers

    NASA Astrophysics Data System (ADS)

    Petrova, T. I.; Dyachenko, F. V.; Bogatyreva, Yu. V.; Borodastov, A. K.; Ershova, I. S.

    2016-05-01

    Effect of compounds involved in complex reagents is described using Helamin 906H reagent as an example. The working exchange capacity of KU-2-8chs cation exchanger in hydrogen form and Amberlite IRA 900Cl anion exchanger in OH form remained almost unchanged when they were used repeatedly to purify water that contained Helamin 906H reagent; in addition, this capacity was the same upon filtration of water that did not contain this reagent. Leakage of total organic carbon was observed earlier than that of calcium ions upon filtration of the solution through the cation exchanger layer. The test results obtained in industrial conditions indicated that using H-OH filters to purify turbine condensate enables the decrease of the concentration of organic and other impurities therein.

  18. Organic ion exchange resin separation methods evaluation

    SciTech Connect

    Witwer, K.S.

    1998-05-27

    This document describes testing to find effective methods to separate Organic Ion Exchange Resin (OIER) from a sludge simulant. This task supports a comprehensive strategy for treatment and processing of K-Basin sludge. The simulant to be used resembles sludge that has accumulated in the 105KE and 105KW Basins in the 1OOK area of the Hanford Site. The sludge is an accumulation of fuel element corrosion products, organic and inorganic ion exchange materials, canister gasket materials, iron and aluminum corrosion products, sand, dirt, and other minor amounts of organic matter.

  19. Cesium-specific phenolic ion exchange resin

    DOEpatents

    Bibler, J.P.; Wallace, R.M.

    1995-08-15

    A phenolic, cesium-specific, cation exchange resin is prepared by neutralizing resorcinol with potassium hydroxide, condensing/polymerizing the resulting intermediate with formaldehyde, heat-curing the resulting polymer to effect cross-linking and grinding it to desired particle size for use. This resin will selectively and efficiently adsorb cesium ions in the presence of a high concentration of sodium ions with a low carbon to cesium ratio. 2 figs.

  20. Cesium-specific phenolic ion exchange resin

    DOEpatents

    Bibler, Jane P.; Wallace, Richard M.

    1995-01-01

    A phenolic, cesium-specific, cation exchange resin is prepared by neutralizing resorcinol with potassium hydroxide, condensing/polymerizing the resulting intermediate with formaldehyde, heat-curing the resulting polymer to effect cross-linking and grinding it to desired particle size for use. This resin will selectively and efficiently adsorb cesium ions in the presence of a high concentration of sodium ions with a low carbon to cesium ratio.

  1. Waste separation and pretreatment using crystalline silicotitanate ion exchangers

    SciTech Connect

    Tadros, M.E.; Miller, J.E.; Anthony, R.G.

    1997-10-01

    A new class of inorganic ion exchangers called crystalline silicotitanates (CSTs) has been developed jointly by Sandia National Laboratories and Texas A&M University to selectively remove Cs and other radionuclides from a wide spectrum of radioactive defense wastes. The CST exhibits high selectivity and affinity for Cs and Sr under a wide range of conditions. Tests show it can remove part-per-million concentrations of Cs{sup +} from highly alkaline, high-sodium simulated radioactive waste solutions modeled after those at Hanford, Oak Ridge, and Savannah River. The materials exhibit ion exchange properties based on ionic size selectivity. Specifically, crystalline lattice spacing is controlled to be highly selective for Cs ions even in waste streams containing very high (5 to 10 M) concentrations of sodium. The CST technology is being demonstrated with actual waste at several DOE facilities. The use of inorganic ion exchangers. The inorganics are more resistant to chemical, thermal, and radiation degradation. Their high selectivities result in more efficient operations offering the possibility of a simple single-pass operation. In contrast, regenerable organic ion exchangers require additional processing equipment to handle the regeneration liquids and the eluant with the dissolved Cs.

  2. Ion Exchange Strengthening of a Leucite-Reinforced Dental Ceramic

    DTIC Science & Technology

    2011-07-28

    total number due to more rapid and efficient sintering . Firing time and temperature parameters also can affect the sizes of internal flaws (Jones, 1983...technique differs from subsequent techniques in that: 1) ion exchange is conducted at temperatures above the transition temperature of the glass, and 2) a...strength increases obtained were attributed to differences in glass transition temperatures (Tg), which in turn were attributed to differing chemical

  3. Liquid membrane coated ion-exchange column solids

    DOEpatents

    Barkey, Dale P.

    1989-01-01

    This invention relates to a method for improving the performance of liquid embrane separations by coating a liquid membrane onto solid ion-exchange resin beads in a fixed bed. Ion-exchange beads fabricated from an ion-exchange resin are swelled with water and are coated with a liquid membrane material that forms a film over the beads. The beads constitute a fixed bed ion-exchange column. Fluid being treated that contains the desired ion to be trapped by the ion-exchange particle is passed through the column. A carrier molecule, contained in the liquid membrane ion-exchange material, is selected for the desired ion in the fluid. The carrier molecule forms a complex with the desired ion, transporting it through the membrane and thus separating it from the other ions. The solution is fed continuously until breakthrough occurs at which time the ion is recovered, and the bed is regenerated.

  4. Liquid membrane coated ion-exchange column solids

    DOEpatents

    Barkey, Dale P.

    1988-01-01

    This invention relates to a method for improving the performance of liquid membrane separations by coating a liquid membrane onto solid ion-exchange resin beads in a fixed bed. Ion-exchange beads fabricated from an ion-exchange resin are swelled with water and are coated with a liquid membrane material that forms a film over the beads. The beads constitute a fixed bed ion-exchange column. Fluid being treated that contains the desired ion to be trapped by the ion-exchange particle is passed through the column. A carrier molecule, contained in the liquid membrane ion-exchange material, is selective for the desired ion in the fluid. The carrier molecule forms a complex with the desired ion, transporting it through the membrane and thus separating it from the other ions. The solution is fed continuously until breakthrough occurs at which time the ion is recovered, and the bed is regenerated.

  5. 25th anniversary article: Ion exchange in colloidal nanocrystals.

    PubMed

    Gupta, Shuchi; Kershaw, Stephen V; Rogach, Andrey L

    2013-12-23

    We review the progress in ion exchange in a variety of nanocrystal structures from the earliest accounts dating back over two decades ago to the present day. In recent years the number of groups using this method to form otherwise difficult or inaccessible nanoparticle shapes and morphologies has increased considerably and the field has experienced a resurgence of interest. Whilst most of the early work on cation exchange centered on II-VI materials, the methodology has been expanded to cover a far broader range of semiconductor nanocrystals including low toxicity I-III-VI materials and the much less facile III-V materials. The extent of exchange can be controlled leading to lightly doped nanoparticles, alloys, core-shells, segmented rods and dots-in-rods. Progress has been driven by a better understanding of the underlying principles of the exchange process - from thermodynamic factors (differences in cation solubilities); the interactions between ions and transfer agents (solvents, ligands, anions, co-dopants); ionic in-diffusion mechanisms and kinetics. More recent availability of very detailed electron microscopy coupled with image reconstruction techniques has been a valuable tool to investigate the resulting heterostructures and internal interfaces. We start by surveying the range of synthetic approaches most often used to carry out ion exchange, mainly focusing on cation replacement strategies, and then describe the rich variety of nanostructures these techniques can bring forth. We also describe some of the principles that are used to establish the relative ease of exchange and to systematically improve the process where the basic energetics are less favorable. To help further the understanding of the underlying fundamentals we have gathered together useful data from the literature on solubilities, cation and anion hardness, ligand and solvent Lewis acid or base strengths for a wide range of chemical species generally used. We offer a perspective on the

  6. An Empirical Formula From Ion Exchange Chromatography and Colorimetry.

    ERIC Educational Resources Information Center

    Johnson, Steven D.

    1996-01-01

    Presents a detailed procedure for finding an empirical formula from ion exchange chromatography and colorimetry. Introduces students to more varied techniques including volumetric manipulation, titration, ion-exchange, preparation of a calibration curve, and the use of colorimetry. (JRH)

  7. ION EXCHANGE ADSORPTION PROCESS FOR PLUTONIUM SEPARATION

    DOEpatents

    Boyd, G.E.; Russell, E.R.; Taylor, M.D.

    1961-07-11

    Ion exchange processes for the separation of plutonium from fission products are described. In accordance with these processes an aqueous solution containing plutonium and fission products is contacted with a cation exchange resin under conditions favoring adsorption of plutonium and fission products on the resin. A portion of the fission product is then eluted with a solution containing 0.05 to 1% by weight of a carboxylic acid. Plutonium is next eluted with a solution containing 2 to 8 per cent by weight of the same carboxylic acid, and the remaining fission products on the resin are eluted with an aqueous solution containing over 10 per cent by weight of sodium bisulfate.

  8. Porous solid ion exchange wafer for immobilizing biomolecules

    DOEpatents

    Arora, Michelle B.; Hestekin, Jamie A.; Lin, YuPo J.; St. Martin, Edward J.; Snyder, Seth W.

    2007-12-11

    A porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer. Also disclosed is a porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer containing a biomolecule with a tag. A separate bioreactor is also disclosed incorporating the wafer described above.

  9. 21 CFR 173.21 - Perfluorinated ion exchange membranes.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Perfluorinated ion exchange membranes. 173.21... Polymer Adjuvants for Food Treatment § 173.21 Perfluorinated ion exchange membranes. Substances identified in paragraph (a) of this section may be safely used as ion exchange membranes intended for use in...

  10. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ion-exchange resins. 173.25 Section 173.25 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.25 Ion-exchange resins. Ion-exchange resins may be safely used in the treatment of food under the following prescribed conditions: (a) The...

  11. 21 CFR 173.21 - Perfluorinated ion exchange membranes.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Perfluorinated ion exchange membranes. 173.21... ion exchange membranes. Substances identified in paragraph (a) of this section may be safely used as ion exchange membranes intended for use in the treatment of bulk quantities of liquid food under...

  12. 21 CFR 173.21 - Perfluorinated ion exchange membranes.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Perfluorinated ion exchange membranes. 173.21... ion exchange membranes. Substances identified in paragraph (a) of this section may be safely used as ion exchange membranes intended for use in the treatment of bulk quantities of liquid food under...

  13. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ion-exchange resins. 173.25 Section 173.25 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.25 Ion-exchange resins. Ion-exchange resins may be safely used in the treatment of food under the following prescribed conditions: (a) The...

  14. 21 CFR 173.21 - Perfluorinated ion exchange membranes.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Perfluorinated ion exchange membranes. 173.21... ion exchange membranes. Substances identified in paragraph (a) of this section may be safely used as ion exchange membranes intended for use in the treatment of bulk quantities of liquid food under...

  15. 21 CFR 173.21 - Perfluorinated ion exchange membranes.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Perfluorinated ion exchange membranes. 173.21... ion exchange membranes. Substances identified in paragraph (a) of this section may be safely used as ion exchange membranes intended for use in the treatment of bulk quantities of liquid food under...

  16. Charge exchange lifetimes for ions in the magnetosphere

    NASA Technical Reports Server (NTRS)

    Smith, P. H.; Bewtra, N. K.

    1977-01-01

    Latest and best measurements of physical quantities involved in complete calculation of the charge exchange lifetime of mirroring magnetospheric ions are coalesced and summarized. It is critical that the charge exchange lifetimes for ions be known as accurately as possible in order to apply the charge exchange mechanism to ion phenomena within the earth's magnetosphere.

  17. PRTR ion exchange vault water removal

    SciTech Connect

    Ham, J.E.

    1995-11-01

    This report documents the removal of radiologically contaminated water from the Plutonium Recycle Test Reactor (PRTR) ion exchange vault. Approximately 57,000 liters (15,000 gallons) of water had accumulated in the vault due to the absence of a rain cover. The water was removed and the vault inspected for signs of leakage. No evidence of leakage was found. The removal and disposal of the radiologically contaminated water decreased the risk of environmental contamination.

  18. Cesium and strontium ion specific exchangers

    SciTech Connect

    Yates, S.

    1996-10-01

    This work is one of two parallel projects that are part of an ESP task to develop high-capacity, selective, solid extractants for cesium, strontium, and technetium from nuclear wastes. In this subtask, Pacific Northwest National Laboratory (PNNL) is collaborating with AlliedSignal, Inc. (Des Plaines, Illinois) to develop inorganic ion exchangers that are selective for strontium and cesium from alkaline high-level waste and groundwater streams.

  19. Cellulosic ion-exchange membranes for hemodialysis.

    PubMed

    Mollison, A N; Graydon, W F

    1977-07-01

    The application of cellulosic ion-exchange membranes to hemodialysis was studied in vitro. The membranes were prepared by radiation-grafting methacrylic acid and vinylpyridine to films of DuPont cellophane PD-215 to produce cation-exchange and anion-exchange membranes, respectively. Solutions of urea, creatinine, glucose, and uric acid were studied for their interactions with and diffusion through the membranes. Ultrafiltration rates were also determined. Cuprophane and PD-215 cellophane were studied as controls. Dialysis plots for the membranes revealed a mechanism of "assisted transport." Initially, the solutes were removed from solution by a sorption/adsorption mechanism followed by a steady-state diffusion process. The calculated diffusivities for these later steady-state regions increased linearly with capacity for urea, creatinine, and uric acid, while for glucose the reverse was true. The combined processes involved provided considerably greater mass transport per unit thickness than either DuPont PD-215 cellophane or Cupropane.

  20. Novel tetrazole-functionalized ion exchanger for weak cation-exchange chromatography of proteins.

    PubMed

    Lei, Genhu; Xiong, Xiaohu; Wei, Yinmao; Zheng, Xiaohui; Zheng, Jianbin

    2008-04-11

    A new type of weak cation exchanger, tetrazole-functionalized silica, was developed for bioseparation. It was prepared conveniently by modifying silica gel initially with gamma-glycidoxypropyltrimethoxysilane, then with 3-hydroxypropionitrile and finally with ammonium-catalyzed (3+2) azide-nitrile cycloaddition, which is an element of click chemistry. The prepared stationary phase was characterized and evaluated for its separation performance, protein retention behavior, loading capacity, protein recovery and chemical stability. The results show that the stationary phase developed has excellent performance for protein separations with high mass recoveries, and has long-term stability. Some remarkable differences were observed between this new exchanger and a carboxylic methyl-functionalized ion exchanger, which is typically used in weak cation-exchange chromatography of proteins. The obtained column was also used for the purification of lysozyme from chicken egg white, and the purity and specific bioactivity of the obtained lysozyme were about 90% and 67 IU/mg, respectively.

  1. Features of ion transport in perfluorinated ion-exchange membranes

    SciTech Connect

    Timashev, S.F.

    1986-02-01

    The conditions for functioning for various systems and devices electrolyzers for ''chlorate'' electrolysis, current sources, etc.) with perfluorinated ion-exchange membranes and septums are determined to a considerable degree by the physicochemical properties of the perfluorinated materials. In this work, on the basis of concepts developed in streaming theory as to the topology of the ''infinite clusters'' (ICs), the author defines more precisely the form of the preexponential dependence of ion transport coefficients and draws conclusions on the character of heat evolution in a perfluorinated membrane when an electric current is passed through the membrane.

  2. Radiation degradation in EPICOR-2 ion exchange resins

    SciTech Connect

    McConnell, J.W. Jr.; Johnson, D.A.; Sanders, R.D. Sr.

    1990-09-01

    The Low-Level Waste Data base Development -- EPICOR-II Resin/Liner Investigation Program funded by the US Nuclear Regulatory Commission is investigating chemical and physical conditions for organic ion exchange resins contained in several EPICOR-II prefilters. Those prefilters were used during cleanup of contaminated water from the Three Mile Island Nuclear Power Station after the March 1979 accident. The work was performed by EG G Idaho, Inc. at the Idaho Engineering Laboratory. This is the final report of this task and summarizes results and analyses of three samplings of ion exchange resins from prefilters PF-8 and -20. Results are compared with baseline data from tests performed on unirradiated resins supplied by Epicor, Inc. to determine the extent of degradation due to the high internal radiation dose received by the organic resins. Results also are compared with those of other researchers. 18 refs., 23 figs., 7 tabs.

  3. Water Exchange Rates and Molecular Mechanism around Aqueous Halide Ions

    SciTech Connect

    Annapureddy, Harsha V.; Dang, Liem X.

    2014-07-17

    Molecular dynamics simulations were performed to systematically study the water-exchange mechanism around aqueous chloride, bromide, and iodide ions. Transition state theory, Grote-Hynes theory, and the reactive flux method were employed to compute water exchange rates. We computed the pressure dependence of rate constants and the corresponding activation volumes to investigate the mechanism of the solvent exchange event. The activation volumes obtained using the transition state theory rate constants are negative for all the three anions, thus indicating an associative mechanism. Contrary to the transition state theory results, activation volumes obtained using rate constants from Grote-Hynes theory and the reactive flux method are positive, thus indicating a dissociative mechanism. The Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences (BES), of the U.S. Department of Energy (DOE) funded this work. Battelle operates Pacific Northwest National Laboratory for DOE. The calculations were carried out using computer resources provided by BES.

  4. Novel silica-based ion exchange resin

    SciTech Connect

    1997-11-01

    Eichrom`s highly successful Diphonixo resin resembles a conventional ion exchange resin in its use of sulfonic acid ligands on a styrene- divinylbenzene matrix. Diphonix resin exhibits rapid exchange kinetics that allow economical operation of ion exchange systems. Unlike conventional resins, Diphonix resin contains chelating ligands that are diphosphonic acid groups that recognize and remove the targeted metals and reject the more common elements such as sodium, calcium and magnesium. This latter property makes Diphonix ideal for many industrial scale applications, including those involving waste treatment. For treatment of low-level, transuranic (TRU) and high- level radioactive wastes, Diphonix`s polystyrene backbone hinders its application due to radiolytic stability of the carbon-hydrogen bonds and lack of compatibility with expected vitrification schemes. Polystyrene-based Diphonix is approximately 60% carbon- hydrogen. In response to an identified need within the Department of Energy for a resin with the positive attributes of Diphonix that also exhibits greater radiolytic stability and final waste form compatibility, Eichrom has successfully developed a new, silica-based resin version of Diphonix. Target application for this new resin is for use in environmental restoration and waste management situations involving the processing of low-level, transuranic and high-level radioactive wastes. The resin can also be used for processing liquid mixed waste (waste that contains low level radioactivity and hazardous constituents) including mixed wastes contaminated with organic compounds. Silica-based Diphonix is only 10% carbon-hydrogen, with the bulk of the matrix silica.

  5. Anion exchangers with branched functional ion exchange layers of different hydrophilicity for ion chromatography.

    PubMed

    Shchukina, O I; Zatirakha, A V; Smolenkov, A D; Nesterenko, P N; Shpigun, O A

    2015-08-21

    Novel polystyrene-divinylbenzene (PS-DVB) based anion exchangers differing from each other in the structure of the branched functional ion exchange layer are prepared to investigate the role of linker and functional site on ion exchange selectivity. The proposed method of synthesis includes the obtaining of aminated PS-DVB particles by means of their acylation with following reductive amination with methylamine. Further modification of the obtained secondary aminogroups is provided by the alkylation with either 1,4-butanediol diglycidyl ether (1,4-BDDGE) or resorcinol diglycidyl ether (RDGE), which form the linkers of different hydrophobicity, and amination of terminal epoxide rings with trimethylamine (TMA), dimethylethanolamine (DMEA), methyldiethanolamine (MDEA) or triethanolamine (TEA). The variation of the structure and hydrophobicity of the linker and terminal quaternary ammonium sites in the functional layer allows the alteration of selectivity and separation efficiency of the obtained adsorbents. The ion exchange selectivity and separation efficiency of the anion exchangers are evaluated using the model mixtures of anions (F(-), HCOO(-), Cl(-), NO2(-), Br(-), NO3(-), HPO4(2-) and SO4(2-)) in potassium hydroxide eluents. The adsorbents show the decrease of selectivity with increasing the hydrophilicity of the terminal functional site. The anion exchangers having more flexible and hydrophilic 1,4-BDDGE linker provide smaller separation factors for most of the analytes as compared with RDGE-containing adsorbents with the same terminal ion exchange sites, but are characterized with higher column efficiencies and better peak symmetry for polarizable anions. In case of 1,4-BDDGE-modified anion exchangers of the particle size of 3.3μm functionalized with DMEA and MDEA the calculated values of column efficiencies for polarizable NO3(-) and Br(-) are up to 49,000 and 53,000N/m, respectively, which is almost twice higher than the values obtained for the RDGE

  6. Ion exchange in hydroxyapatite with lanthanides.

    PubMed

    Cawthray, Jacqueline F; Creagh, A Louise; Haynes, Charles A; Orvig, Chris

    2015-02-16

    Naturally occurring hydroxyapatite, Ca5(PO4)3(OH) (HAP), is the main inorganic component of bone matrix, with synthetic analogues finding applications in bioceramics and catalysis. An interesting and valuable property of both natural and synthetic HAP is the ability to undergo cationic and anionic substitution. The lanthanides are well-suited for substitution for the Ca(2+) sites within HAP, because of their similarities in ionic radii, donor atom requirements, and coordination geometries. We have used isothermal titration calorimetry (ITC) to investigate the thermodynamics of ion exchange in HAP with a representative series of lanthanide ions, La(3+), Sm(3+), Gd(3+), Ho(3+), Yb(3+) and Lu(3+), reporting the association constant (Ka), ion-exchange thermodynamic parameters (ΔH, ΔS, ΔG), and binding stoichiometry (n). We also probe the nature of the La(3+):HAP interaction by solid-state nuclear magnetic resonance ((31)P NMR), X-ray diffraction (XRD), and inductively coupled plasma-optical emission spectroscopy (ICP-OES), in support of the ITC results.

  7. Impact of the electrochemical porosity and chemical composition on the lithium ion exchange behavior of polypyrroles (ClO4-, TOS-, TFSI-) prepared electrochemically in propylene carbonate. comparative EQCM, EIS and CV studies.

    PubMed

    Dziewoński, Paweł Marek; Grzeszczuk, Maria

    2010-06-03

    Conditions of electrodeposition, i.e. a potential window of the process, addition of water, the current density, and morphology of substrate electrodes (Pt, Pt/TiO(2), Au), were shown to influence strongly ion-exchange properties of polypyrrole (PPy) synthesized in propylene carbonate (PC), doped with ClO(4)(-) or p-toluenesulfonate (TOS(-)). "Electrochemical porosity" and redox activity of PPy films were compared to the characteristics of poly(3,4-ethylenedioxythiophene) (PEDOT). A molecular indicator of the PPy film structure packing was bis(trifluoromethylsulfonyl)imide anion (TFSI(-)). Ion-exchange properties of PPy were found to be almost independent of chemical composition of the polymer, described in the literature as PPy(I), PPy(II), PPy(III). Instead, micro- and nanoscopic morphology of the polymer film and a molecular level packing of the polymer chains as well as the counterion nature are of the foremost importance. The polymer film structure/properties are shown to change upon prolonged redox/ionic stimulations. Lithium exchange between PPy films and contacting phases (PC electrolyte, TiO(2)) proceeds in addition to the anion exchange, the latter being a dominant process under conditions of the reversible electrochemical p-doping of PPy, although diffusion coefficients of PC solvated lithium ions in PPy are higher than diffusion coefficients of perchlorate, p-toluenesulfonate or bis(trifluoromethylsulfonyl)imide anions. The highest flux of Li(+) ions into/out of the PPy phase takes place about -1.0 V vs Ag/Ag(+) which is clearly evidenced by the cathodic/anodic CV peaks. Cation transport phenomena can be analyzed independently from anion transport when observed at a longer time scale (low values of potential scan rate) as each prevails at different redox states of the polymer. However, in a shorter time scale (v > or = 10 mV s(-1)), the opposite fluxes of cations and anions were observed to interfere. Furthermore, a net uptake of propylene carbonate by

  8. Solidification of ion exchange resin wastes

    SciTech Connect

    Not Available

    1982-08-01

    Solidification media investigated included portland type I, portland type III and high alumina cements, a proprietary gypsum-based polymer modified cement, and a vinyl ester-styrene thermosetting plastic. Samples formulated with hydraulic cement were analyzed to investigate the effects of resin type, resin loading, waste-to-cement ratio, and water-to-cement ratio. The solidification of cation resin wastes with portland cement was characterized by excessive swelling and cracking of waste forms, both after curing and during immersion testing. Mixed bed resin waste formulations were limited by their cation component. Additives to improve the mechanical properties of portland cement-ion exchange resin waste forms were evaluated. High alumina cement formulations dislayed a resistance to deterioration of mechanical integrity during immersion testing, thus providing a significant advantage over portland cements for the solidification of resin wastes. Properties of cement-ion exchange resin waste forms were examined. An experiment was conducted to study the leachability of /sup 137/Cs, /sup 85/Sr, and /sup 60/Co from resins modified in portland type III and high alumina cements. The cumulative /sup 137/Cs fraction release was at least an order of magnitude greater than that of either /sup 85/Sr or /sup 60/Co. Release rates of /sup 137/Cs in high alumina cement were greater than those in portland III cement by a factor of two.Compressive strength and leach testing were conducted for resin wastes solidified with polymer-modified gypsum based cement. /sup 137/Cs, /sup 85/Sr, and /sup 60/Co fraction releases were about one, two and three orders of magnitude higher, respectively, than in equivalent portland type III cement formulations. As much as 28.6 wt % dry ion exchange resin was successfully solidified using vinyl ester-styrene compared with a maximum of 25 wt % in both portland and gypsum-based cement.

  9. Biodegradation of ion-exchange media

    SciTech Connect

    Bowerman, B.S.; Clinton, J.H.; Cowdery, S.R.

    1988-01-01

    The purpose of this study was to investigate further the potential for ion-exchange media (resin beads or powdered filter media) to support biological growth. A mixed microbial culture was grown from resin wastes obtained from the BNL HFBR by mixing the resin with a nutrient salt solution containing peptone and yeast extract. Bacterial and fungal growths appeared in the solution and on the resins after 7 to 10 days incubation at 337)degree)C. The mixed microbial cultures were used to inoculate several resin types, both irradiated and unirradiated. 12 refs., 5 tabs.

  10. Ion exchange polymers and method for making

    NASA Technical Reports Server (NTRS)

    Philipp, Warren H. (Inventor); Street, Kenneth W., Jr. (Inventor)

    1994-01-01

    An ion exchange polymer comprised of an alkali metal or alkaline earth metal salt of a poly(carboxylic acid) in a poly(vinyl acetal) matrix is described. The polymer is made by treating a mixture made of poly(vinyl alcohol) and poly(acrylic acid) with a suitable aldehyde and an acid catalyst to cause acetalization with some cross-linking. The material is then subjected to an alkaline aqueous solution of an alkali metal salt or an alkali earth metal salt. All of the film forming and cross-linking steps can be carried out simultaneously, if desired.

  11. Ion exchange extraction of heavy metals from wastewater sludges.

    PubMed

    Al-Enezi, G; Hamoda, M F; Fawzi, N

    2004-01-01

    Heavy metals are common contaminants of some industrial wastewater. They find their way to municipal wastewaters due to industrial discharges into the sewerage system or through household chemicals. The most common heavy metals found in wastewaters are lead, copper, nickel, cadmium, zinc, mercury, arsenic, and chromium. Such metals are toxic and pose serious threats to the environment and public health. In recent years, the ion exchange process has been increasingly used for the removal of heavy metals or the recovery of precious metals. It is a versatile separation process with the potential for broad applications in the water and wastewater treatment field. This article summarizes the results obtained from a laboratory study on the removal of heavy metals from municipal wastewater sludges obtained from Ardhiya plant in Kuwait. Data on heavy metal content of the wastewater and sludge samples collected from the plant are presented. The results obtained from laboratory experiments using a commercially available ion exchange resin to remove heavy metals from sludge were discussed. A technique was developed to solubilize such heavy metals from the sludge for subsequent treatment by the ion exchange process. The results showed high efficiency of extraction, almost 99.9%, of heavy metals in the concentration range bound in wastewater effluents and sludges. Selective removal of heavy metals from a contaminated wastewater/sludge combines the benefits of being economically prudent and providing the possibility of reuse/recycle of the treated wastewater effluents and sludges.

  12. Isotopic exchange of uranium. II. Exchange kinetics in solution-organic-ion exchanger systems

    SciTech Connect

    Ryzhinskii, M.V.; Bronzov, P.A.; Vitinskii, M.Yu.

    1987-07-01

    The results of a study of the sorption of uranium and the kinetics of isotopic exchange between uranium(IV) and uranium(VI) in systems consisting of a hydrochloric acid solution and the KU-2-8P and AV-17-10P ion-exchange resins have been studied. It has been shown that the sorption of uranium is limited by diffusion in the sorbent grains and that isotopic exchange is limited by the reaction between uranium(IV) and uranium(VI).

  13. Ion Exchange Chromatography and Spectrophotometry: An Introductory Undergraduate Laboratory Experiment.

    ERIC Educational Resources Information Center

    Foster, N.; And Others

    1985-01-01

    Describes an experiment in which students use ion exchange chromatography to separate a mixture of chloro complexes of transition metal ions and then use spectrophotometry to define qualitatively the efficiency of the ion exchange columns. Background information, materials needed, and procedures used are included. (JN)

  14. Multicomponent liquid ion exchange with chabazite zeolites

    SciTech Connect

    Robinson, S.M.; Arnold, W.D. Jr.; Byers, C.W.

    1993-10-01

    In spite of the increasing commercial use of zeolites for binary and multicomponent sorption, the understanding of the basic mass-transfer processes associated with multicomponent zeolite ion-exchange systems is quite limited. This study was undertaken to evaluate Na-Ca-Mg-Cs-Sr ion exchange from an aqueous solution using a chabazite zeolite. Mass-transfer coefficients and equilibrium equations were determined from experimental batch-reactor data for single and multicomponent systems. The Langmuir isotherm was used to represent the equilibrium relationship for binary systems, and a modified Dubinin-Polyani model was used for the multicomponent systems. The experimental data indicate that diffusion through the microporous zeolite crystals is the primary diffusional resistance. Macropore diffusion also significantly contributes to the mass-transfer resistance. Various mass-transfer models were compared to the experimental data to determine mass-transfer coefficients. Effective diffusivities were obtained which accurately predicted experimental data using a variety of models. Only the model which accounts for micropore and macropore diffusion occurring in series accurately predicted multicomponent data using single-component diffusivities. Liquid and surface diffusion both contribute to macropore diffusion. Surface and micropore diffusivities were determined to be concentration dependent.

  15. Radionuclide Leaching from Organic Ion Exchange Resin

    SciTech Connect

    Delegard, C.H.; Rinehart, D.E.

    1999-04-02

    Laboratory tests were performed to examine the efficacy of leach treatments for decontaminating organic ion exchange resins (OIER), which have been found in a number of samples retrieved from K East Basin sludge. Based on process records, the OIER found in the K Basins is a mixed-bet strong acid/strong base material marketed as Purolite{trademark} NRW-037. Radionuclides sorbed or associated with the OIER can restrict its disposal to the Environmental Restoration Disposal Facility (ERDF). The need for testing to support development of a treatment process for K Basin sludge has been described in Section 4.2 of ''Testing Strategy to Support the Development of K Basins Sludge Treatment Process'' (Flament 1998). To help understand the effects of anticipated OIER elutriation and washing, tests were performed with well-rinsed OIER material from K East Basin floor sludge (sample H-08 BEAD G) and with well-rinsed OIER having approximately 5% added K East canister composite sludge (sample KECOMP). The rinsed resin-bearing material also contained the inorganic ion exchanger Zeolon-900{trademark}, a zeolite primarily composed of the mineral mordenite. The zeolite was estimated to comprise 27 weight percent of the dry H-08 BEAD G material.

  16. [Ion-exchange hemosorption in the intensive therapy of liver insufficiency in patients with obstructive jaundice].

    PubMed

    Minina, K Z; Kurapov, E P; Goncharov, V V; Leĭkin, Iu A; Tarasova, T I; Treushnikova, N Iu

    1989-01-01

    Hemosorption on thromboresistant ion-exchange resins synthetized at D. I. Mendeleev Moscow Chemical Technological Institute (MCTI) was used in combined therapy of hepatic failure. Use was made of anion-exchange resin A-I-II MCTI, catonit C-I-II MCTI, polyampholit. Stability of hemodynamic parameters, absence of blood element disturbances, effective sampling of anionic and cationic metabolites have been observed.

  17. Brown coals as natural electron-ion-exchangers

    SciTech Connect

    Kossov, I.I.; Aleksandrov, I.V.; Kamneva, A.I.

    1984-01-01

    The existence of electron-ion-exchange properties in brown coals has been established. The influence of the redox properties of the organic and mineral fractions of the coals on their capacity for electron exchange has been shown.

  18. Ion-exchange polymer artificial muscle and actuating system

    NASA Astrophysics Data System (ADS)

    Vial, Dominique; Tondu, Bertrand; Lopez, Pierre; Aurelle, Yves; Ricard, Alain

    1996-04-01

    Chemomechanical transformations are used to produce a mechanical force from a reversible chemical reaction in order to generate artificial muscular contraction, on the model of the biological muscle. The design and experimentation of an original artificial muscle using an ion-exchange polymer which reacts inside a soft envelope, derived from research on pneumatic artificial McKibben muscle, is presented. Then a chemomechanical actuator constituted of two artificial muscles has been conceived: first results are shown on position control in open-loop mode.

  19. Mineral Separation in a CELSS by Ion-exchange Chromatography

    NASA Technical Reports Server (NTRS)

    Ballou, E. V.; Spitze, L. A.; Wong, F. W.; Wydeven, T.; Johnson, C. C.

    1982-01-01

    Operational parameters pertinent to ion exchange chromatography separation were identified. The experiments were performed with 9 mm diameter ion exchange columns and conventional column accessories. The cation separation beds were packed with AG 50W-X2 strong acid cation exchange resin in H(+) form and 200-400 dry mesh particle size. The stripper beds used in some experiments were packed with AG 1-XB strong base cation exchange resin in OH(-) form and 200-400 dry mesh particle size.

  20. Separation of uranium isotopes by chemical exchange

    DOEpatents

    Ogle, P.R. Jr.

    1974-02-26

    A chemical exchange method is provided for separating /sup 235/U from / sup 238/U comprising contacting a first phase containing UF/sub 6/ with a second phase containing a compound selected from the group consisting of NOUF/sub 6/, NOUF/sub 7/, and NO/sub 2/UF/sub 7/ until the U Fsub 6/ in the first phase becomes enriched in the /sup 235/U isotope. (Official Gazette)

  1. Stabilization of copper nanoparticles with volume- and surface-distribution inside ion-exchange matrices

    NASA Astrophysics Data System (ADS)

    Kravchenko, T. A.; Sakardina, E. A.; Kalinichev, A. I.; Zolotukhina, E. V.

    2015-09-01

    Nanocomposites characterized by the surface and volume distributions of deposited copper nanoparticles are obtained via the chemical deposition of copper onto sulfonic acid and carboxylic cation exchanger and strongly basic anion exchanger matrices. The electrode behavior of the synthesized composites in CuSO4 solution is studied by open-circuit chronopotentiometry. The effect the nature of the fixed centers of the ion-exchange matrix has on the initial state of metallic particles and the processes that occur in solutions of their metal ions is established from the deviation of the nanocomposites' electrode potential from the potential of a compact electrode and the nature of its change over time. It is shown that the mechanism behind the interaction of the matrix and metal ions (ion exchange, non-exchange absorption, complexation) determines not only the initial size and distribution of metal particles, but also the rate at which they achieve aggregative stability.

  2. Effects of ionizing radiation on modern ion exchange materials

    SciTech Connect

    Marsh, S.F.; Pillay, K.K.S.

    1993-10-01

    We review published studies of the effects of ionizing radiation on ion exchange materials, emphasizing those published in recent years. A brief overview is followed by a more detailed examination of recent developments. Our review includes styrene/divinylbenzene copolymers with cation-exchange or anion-exchange functional groups, polyvinylpyridine anion exchangers, chelating resins, multifunctional resins, and inorganic exchangers. In general, strong-acid cation exchange resins are more resistant to radiation than are strong-base anion exchange resins, and polyvinylpyridine resins are more resistant than polystyrene resins. Cross-linkage, salt form, moisture content, and the surrounding medium all affect the radiation stability of a specific exchanger. Inorganic exchangers usually, but not always, exhibit high radiation resistance. Liquid ion exchangers, which have been used so extensively in nuclear processing applications, also are included.

  3. Scintillating 99Tc Selective Ion Exchange Resins

    SciTech Connect

    Mitchell Greenhalgh; Richard D. Tillotson

    2012-07-01

    Scintillating technetium (99Tc) selective ion exchange resins have been developed and evaluated for equilibrium capacities and detection efficiencies. These resins can be utilized for the in-situ concentration and detection of low levels of pertechnetate anions (99TcO4-) in natural waters. Three different polystyrene type resin support materials were impregnated with varying amounts of tricaprylmethylammonium chloride (Aliquat 336) extractant, several different scintillating fluors and wavelength shifters. The prepared resins were contacted batch-wise to equilibrium over a wide range of 99TcO4- concentrations in natural water. The measured capacities were used to develop Langmuir adsorption isotherms for each resin. 99Tc detection efficiencies were determined and up to 71.4 ± 2.6% was achieved with some resins. The results demonstrate that a low level detection limit for 99TcO4- in natural waters can be realized.

  4. Pyrolysis of Spent Ion Exchange Resins - 12210

    SciTech Connect

    Braehler, Georg; Slametschka, Rainer

    2012-07-01

    Organic ion exchangers (IEX) play a major and increasing role in the reactor coolant and other water purification processes. During their operation time they receive significant amounts of radioactivity, making their disposal, together with their organic nature, as medium active waste challenging. Processes applied so far do not eliminate the organic matter, which is unwanted in disposal facilities, or, if high temperatures are applied, raise problems with volatile radionuclides. NUKEM Technologies offers their well introduces process for the destruction of spent solvent (TBP), the pebble bed pyrolysis, now for the treatment of spent IEX (and other problematic waste), with the following benefits: the pyrolysis product is free of organic matter, and the operation temperature with approx. 500 deg. C keeps Cs radionuclides completely in the solid residue. (authors)

  5. TECHNICAL COMPARISON OF CANDIDATE ION EXCHANGE MEDIA FOR SMALL COLUMN ION EXCHANGE (SCIX) APPLICATIONS IN SUPPORT OF SUPPLEMENTAL LAW PRETREATMENT

    SciTech Connect

    RAMSEY AA; THORSON MR

    2010-12-28

    At-tank supplemental pretreatment including both filtration and small column ion exchange is currently under evaluation to facilitate salt waste retrieval and processing in the Hanford tank farms. Spherical resorcinol formaldehyde (sRF) resin is the baseline ion exchange resin for use in the Waste Treatment and Immobilization Plant (WTP). This document provides background and technical rationale to assist in determining whether spherical resorcinol formaldehyde (sRF) is also the appropriate ion exchange resin for supplemental LAW pretreatment processes and compares sRF with crystalline silicotitanate (CST) as potential supplemental pretreatment ion exchange media.

  6. Proton/calcium ion exchange behavior of calcite.

    PubMed

    Villegas-Jiménez, Adrián; Mucci, Alfonso; Paquette, Jeanne

    2009-10-21

    The characterization of the proton sorptive properties of calcite in aqueous solutions at 25 +/- 1 degrees C over a relatively wide range of chemical conditions (7.16 ions is consistently observed, greatly exceeding the theoretical number of reactive surface sites. These observations are interpreted as a fast proton/calcium exchange equilibrium between the solution and "exchangeable cation sites" (e.g., lattice positions) at and/or beneath the calcite surface (species identified by "(exc)"), , that leads to a transient, "apparent" incongruent dissolution regime and the formation of a stable calcium-deficient, proton-enriched layer within the calcite lattice under circum-neutral and alkaline regimes at standard conditions. The 2H(+)/Ca(2+) ion exchange is quantitatively described by the Langmuir-power exchange function under the Vanselow convention: where n = 1 and log(10)K(ex) = 13.0 +/- 0.3. This calcite behavior, never reported before, masks surface equilibria and directly impacts the aqueous speciation of carbonate-rock systems with poor CO(2)(g) ventilation (e.g., aquifers, pore and deep sea waters, industrial reactors) via the buffering of pH and calcite dissolution. In contrast, at fixed pCO(2) conditions, aqueous speciation remains unaffected upon CO(2)(g) sequestration resulting from ion exchange-induced calcite precipitation: ([triple bond]CaCO3)2(exc) + CO2(g) + H2O <==> [triple bond]Ca(HCO3)2(exc) + CaCO3(s). Accordingly, reliable predictions of aqueous speciation in natural or engineered calcite-containing systems at variable pCO(2) conditions must consider this exchange reaction and the associated K(ex). The postulated proton/calcium exchange may have far

  7. Waste treatment by selective mineral ion exchanger

    SciTech Connect

    Polito, Aurelie

    2007-07-01

    STMI, subsidiary company of the AREVA Group with over 40 years in the D and D business, has been continuously innovating and developing new decontamination techniques, with the objectives of achieving more efficient decontaminations on a growing spectrum of media. In the field of liquid waste treatment, STMI manufactures uses and commercialises selective inorganic ion exchangers (RAN). These are hydrated synthetic inorganic compounds prepared from very pure raw materials. Different types of RANs (POLYAN, OXTAIN, Fe-Cu, Fe-CoK, Si-Fe-CoK) can be used to trap a large number of radioactive elements in contaminated effluents. Different implementations could be applied depending on technical conditions. STMI's offers consist in building global solution and preliminary design of installation either in dispersed form (batch) or in column (cartridge filtration). Those products are used all over the world not only in the nuclear business (Canada, US, Belgium, France...) but also in other fields. Indeed, it provides competitive solutions to many domains of application especially water pollution control, liquid waste treatment in the nuclear business by decreasing the activity level of waste. The following paper will focus on the theoretical principle of the mineral exchanger, its implementation and the feed back collected by STMI. (author)

  8. ION EXCHANGE IN FUSED SALTS. II. THE DISTRIBUTION OF ALKALI METAL AND ALKALINE EARTH IONS BETWEEN CHABAZITE AND FUSED LINO3, NANO3, AND KNO3,

    DTIC Science & Technology

    ION EXCHANGE, SALTS ), (*ALKALI METALS, ION EXCHANGE), (*ALKALINE EARTH METALS, ION EXCHANGE), (*NITRATES, ION EXCHANGE), SODIUM , CALCIUM, POTASSIUM...BARIUM, RUBIDIUM, CESIUM, LITHIUM COMPOUNDS, SODIUM COMPOUNDS, POTASSIUM COMPOUNDS, DISTRIBUTION, MINERALS, IONS

  9. Rupture Loop Annex (RLA) ion exchange vault entry and characterization

    SciTech Connect

    Ham, J.E.

    1996-01-04

    This engineering report documents the entry and characterization of the Rupture Loop Annex Ion Exchange (RLAIX) Vault located near the 309 Building`s Plutonium Recycle Test Reactor (PRTR). Twelve ion exchange columns were found in the vault. Some of which contained transuranics, Cs 137, and Co 60. The characterization information is necessary for future vault cleanout and column disposal.

  10. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... CONSUMPTION (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.25 Ion-exchange resins. Ion-exchange resins may be...)(17) of this section is used only for industrial application to treat bulk quantities of aqueous...

  11. Degradation mechanism of sulfonated poly(ether ether ketone) (SPEEK) ion exchange membranes under vanadium flow battery medium.

    PubMed

    Yuan, Zhizhang; Li, Xianfeng; Hu, Jinbo; Xu, Wanxing; Cao, Jingyu; Zhang, Huamin

    2014-10-07

    The degradation mechanism of hydrocarbon ion exchange membranes under vanadium flow battery (VFB) medium was investigated and clarified for the first time. This work will be highly beneficial for improving the chemical stability of hydrocarbon ion exchange membranes, which is one of the most challenging issues for VFB application.

  12. Ion exchange properties of novel hydrous metal oxide materials

    SciTech Connect

    Gardner, T.J.; McLaughlin, L.I.

    1996-12-31

    Hydrous metal oxide (HMO) materials are inorganic ion exchangers which have many desirable characteristics for catalyst support applications, including high cation exchange capacity, anion exchange capability, high surface area, ease of adjustment of acidity and basicity, bulk or thin film preparation, and similar chemistry for preparation of various transition metal oxides. Cation exchange capacity is engineered into these materials through the uniform incorporation of alkali cations via manipulation of alkoxide chemistry. Specific examples of the effects of Na stoichiometry and the addition of SiO{sub 2} to hydrous titanium oxide (HTO) on ion exchange behavior will be given. Acid titration and cationic metal precursor complex exchange will be used to characterize the ion exchange behavior of these novel materials.

  13. Local structures of ions at ion-exchange resin/solution interface.

    PubMed

    Harada, Makoto; Okada, Tetsuo

    2005-08-26

    The local structures of Cl- and Br- in anion-exchange resins have been studied by X-ray absorption fine structure (XAFS), and separation selectivity is discussed on the basis of results. When two different anion-exchange resins having trimethylammonium and dimethylammonium groups as anion-exchange groups are employed for ion-exchange experiments, slightly higher Br- selectivity has been obtained with the former. XAFS has indicated that the average hydration numbers for a given anion is not affected by the structure of the ion-exchange group, but that the extent of ion-association between the anion and the ion-exchange groups depends on the type of the ion-exchange group. Shorter interaction distance (and in turn stronger ion-association) has been confirmed for the dimethylammonium-type resin, and is consistent with lower Br- selectivity of this resin.

  14. Experimental Findings On Minor Actinide And Lanthanide Separations Using Ion Exchange

    SciTech Connect

    Hobbs, D. T.; Shehee, T. C.; Clearfield, A.

    2013-09-17

    This project seeks to determine if inorganic or hybrid inorganic ion-exchange materials can be exploited to provide effective americium and curium separations. Specifically, we seek to understand the fundamental structural and chemical factors responsible for the selectivity of the tested ion-exchange materials for actinide and lanthanide ions. During FY13, experimental work focused in the following areas: (1) investigating methods to oxidize americium in dilute nitric acid with subsequent ion-exchange performance measurements of ion exchangers with the oxidized americium and (2) synthesis, characterization and testing of ion-exchange materials. Ion-exchange materials tested included alkali titanates, alkali titanosilicates, carbon nanotubes and group(IV) metal phosphonates. Americium oxidation testing sought to determine the influence that other redox active components may have on the oxidation of Am(III). Experimental findings indicated that Pu(IV) is oxidized to Pu(VI) by peroxydisulfate, but there are no indications that the presence of plutonium affects the rate or extent of americium oxidation at the concentrations of peroxydisulfate being used. Tests also explored the influence of nitrite on the oxidation of Am(III). Given the formation of Am(V) and Am(VI) in the presence of nitrite, it appears that nitrite is not a strong deterrent to the oxidation of Am(III), but may be limiting Am(VI) by quickly reducing Am(VI) to Am(V). Interestingly, additional absorbance peaks were observed in the UV-Vis spectra at 524 and 544 nm in both nitric acid and perchloric acid solutions when the peroxydisulfate was added as a solution. These peaks have not been previously observed and do not correspond to the expected peak locations for oxidized americium in solution. Additional studies are in progress to identify these unknown peaks. Three titanosilicate ion exchangers were synthesized using a microwave-accelerated reaction system (MARS) and determined to have high affinities

  15. Evaluation of Ion Exchange Materials in K Basin Floor Sludge and Potential Solvents for PCB Extraction from Ion Exchange Materials

    SciTech Connect

    Schmidt, A.J.; Klinger, G.S.; Bredt, P.R.

    1999-04-10

    Approximately 73 m{sup 3} of heterogeneous solid material, ''sludge,'' (upper bound estimate, Packer 1997) have accumulated at the bottom of the K Basins in the 100 K Area of the Hanford Site. This sludge is a mixture of spent fuel element corrosion products, ion exchange materials (organic and inorganic), graphite-based gasket materials, iron and aluminum metal corrosion products, sand, and debris (Makenas et al. 1996, 1997). In addition, small amounts of polychlorinated biphenyls (PCBs) have been found. These small amounts are significant from a regulatory standpoint. Ultimately, it is planned to transfer the K Basins sludge to the Hanford double shell tanks (DSTs). Chemical pretreatment is required to address criticality issues and the destruction or removal of PCBs before the K Basin sludge can be transferred to the DSTs. Eleven technologies have been evaluated (Papp 1997) as potential pretreatment methods. Based on the evaluations and engineering studies and limited testing, Fluor Daniel Hanford recommended solvent washing of the K Basin sludge, followed by nitric acid dissolution and, potentially, peroxide addition (FDH 1997). The solvent washing (extraction) and peroxide addition would be used to facilitate PCB removal and destruction. Following solvent extraction, the PCBs could be distilled and concentrated for disposal as a low-level waste. The purpose of the work reported here was to continue investigating solvent extraction, first by better identifying the ion exchange materials in the actual sludge samples and then evaluating various solvents for removing the PCBs or possibly dissolving the resins. This report documents some of the process knowledge on ion exchange materials used and spilled in the K Basins and describes the materials identified from wet sieving KE Basin floor and canister sludge and the results of other analyses. Several photographs are included to compare materials and illustrate material behavior. A summary of previous tests on

  16. Gadolinium-hydrogen ion exchange of zirconium phosphate

    NASA Technical Reports Server (NTRS)

    Liu, D. C.; Power, J. L.

    1972-01-01

    The Gd(+3)/H(+) ion exchange on a commercial zirconium phosphate ion exchanger was investigated in chloride, sulfate, and phosphate solutions of Gd(+3) at gadolinium concentrations of 0.001 to 1 millimole per cc and in the pH range of 0 to 3.5. Relatively low Gd(+3) capacities, in the range of 0.01 to 0.1 millimole per g of ion exchanger were found at room temperature. A significant difference in Gd(+3) sorption was observed, depending on whether the ion exchanger was converted from initial conditions of greater or lesser Gd(+3) sorption than the specific final conditions. Correlations were found between decrease in Gd(+3) capacity and loss of exchanger phosphate groups due to hydrolysis during washing and between increase in capacity and treatment with H3PO4. Fitting of the experimental data to ideal ion exchange equilibrium expressions indicated that each Gd(+3) ion is sorbed on only one site of the ion exchanger. The selectivity quotient was determined to be 2.5 + or - 0.4 at room temperature on gadolinium desorption in chloride solutions.

  17. Anion exchangers with negatively charged functionalities in hyperbranched ion-exchange layers for ion chromatography.

    PubMed

    Uzhel, Anna S; Zatirakha, Alexandra V; Smirnov, Konstantin N; Smolenkov, Alexandr D; Shpigun, Oleg A

    2017-01-27

    Novel pellicular poly(styrene-divinylbenzene)-based (PS-DVB) anion exchangers with covalently-bonded hyperbranched functional ion-exchange layers containing negatively charged functionalities are obtained and examined. The hyperbranched coating is created on the surface of aminated PS-DVB substrate by repeating the modification cycles including alkylation with 1,4-butanediol diglycidyl ether (1,4-BDDGE), and amination of the terminal epoxide rings with methylamine (MA) or glycine (Gly). The influence of the position and the number of the layers with glycine, as well as of the total number of the layers of amine in the coating on the chromatographic properties of the obtained stationary phases is investigated. Chromatographic performance of the obtained stationary phases is evaluated using the model mixtures of inorganic and organic anions with hydroxide eluent. It is shown that the best selectivity toward weakly retained organic acids and oxyhalides is possessed by the anion exchanger obtained after 5 modification cycles, with glycine being used in the first one. Such anion exchanger packed in 25-cm long column is capable of separating 22 anions in 58min including 7 standard anions, mono-, di- and trivalent organic acids, oxyhalides, and some other double- and triple-charged anions.

  18. Hydrolyzed Poly(acrylonitrile) Electrospun Ion-Exchange Fibers

    PubMed Central

    Jassal, Manisha; Bhowmick, Sankha; Sengupta, Sukalyan; Patra, Prabir K.; Walker, Douglas I.

    2014-01-01

    Abstract A potential ion-exchange material was developed from poly(acrylonitrile) fibers that were prepared by electrospinning followed by alkaline hydrolysis (to convert the nitrile group to the carboxylate functional group). Characterization studies performed on this material using X-ray photoelectron spectroscopy, scanning electron microscopy, Fourier-Transform infra-red spectroscopy, and ion chromatography confirmed the presence of ion-exchange functional group (carboxylate). Optimum hydrolysis conditions resulted in an ion-exchange capacity of 2.39 meq/g. Ion-exchange fibers were used in a packed-bed column to selectively remove heavy-metal cation from the background of a benign, competing cation at a much higher concentration. The material can be efficiently regenerated and used for multiple cycles of exhaustion and regeneration. PMID:24963270

  19. Recent developments on ion-exchange membranes and electro-membrane processes.

    PubMed

    Nagarale, R K; Gohil, G S; Shahi, Vinod K

    2006-02-28

    Rapid growth of chemical and biotechnology in diversified areas fuels the demand for the need of reliable green technologies for the down stream processes, which include separation, purification and isolation of the molecules. Ion-exchange membrane technologies are non-hazardous in nature and being widely used not only for separation and purification but their application also extended towards energy conversion devices, storage batteries and sensors etc. Now there is a quite demand for the ion-exchange membrane with better selectivities, less electrical resistance, high chemical, mechanical and thermal stability as well as good durability. A lot of work has been done for the development of these types of ion-exchange membranes during the past twenty-five years. Herein we have reviewed the preparation of various types of ion-exchange membranes, their characterization and applications for different electro-membrane processes. Primary attention has been given to the chemical route used for the membrane preparation. Several general reactions used for the preparation of ion-exchange membranes were described. Methodologies used for the characterization of these membranes and their applications were also reviewed for the benefit of readers, so that they can get all information about the ion-exchange membranes at one platform. Although there are large number of reports available regarding preparations and applications of ion-exchange membranes more emphasis were predicted for the usefulness of these membranes or processes for solving certain type of industrial or social problems. More efforts are needed to bring many products or processes to pilot scale and extent their applications.

  20. Process parameters optimization in ion exchange 238Pu aqueous processing

    NASA Astrophysics Data System (ADS)

    Pansoy-Hjelvik, M. E.; Nixon, J.; Laurinat, J.; Brock, J.; Silver, G.; Reimus, M.; Ramsey, K. B.

    2000-07-01

    This paper describes bench-scale efforts (5-7 grams of 238Pu) to optimize the ion exchange process for 234U separation with minimal 238Pu losses to the effluent and wash liquids. The bench-scale experiments also determine the methodology to be used for the full-scale process: 5 kg238Pu annual throughput. Heat transfer calculations used to determine the thermal gradients expected during ion exchange processing are also described. The calculations were performed in collaboration with Westinghouse Savannah River Technology Center (WSRTC) and provide information for the design of the full-scale ion exchange equipment.

  1. Ion-exchanged glass waveguide technology: a review

    NASA Astrophysics Data System (ADS)

    Tervonen, Ari; West, Brian R.; Honkanen, Seppo

    2011-07-01

    We review the history and current status of ion exchanged glass waveguide technology. The background of ion exchange in glass and key developments in the first years of research are briefly described. An overview of fabrication, characterization and modeling of waveguides is given and the most important waveguide devices and their applications are discussed. Ion exchanged waveguide technology has served as an available platform for studies of general waveguide properties, integrated optics structures and devices, as well as applications. It is also a commercial fabrication technology for both passive and active wave-guide components.

  2. Advantages of paramagnetic chemical exchange saturation transfer (CEST) complexes having slow to intermediate water exchange properties as responsive MRI agents.

    PubMed

    Soesbe, Todd C; Wu, Yunkou; Dean Sherry, A

    2013-07-01

    Paramagnetic chemical exchange saturation transfer (PARACEST) complexes are exogenous contrast agents that have great potential to further extend the functional and molecular imaging capabilities of magnetic resonance. As a result of the presence of a central paramagnetic lanthanide ion (Ln(3+) ≠ La(3+) , Gd(3+) , Lu(3+) ) within the chelate, the resonance frequencies of exchangeable protons bound to the PARACEST agent are shifted far away from the bulk water frequency. This large chemical shift, combined with an extreme sensitivity to the chemical exchange rate, make PARACEST agents ideally suited for the reporting of significant biological metrics, such as temperature, pH and the presence of metabolites. In addition, the ability to turn PARACEST agents 'off' and 'on' using a frequency-selective saturation pulse gives them a distinct advantage over Gd(3+) -based contrast agents. A current challenge for PARACEST research is the translation of the promising in vitro results into in vivo systems. This short review article first describes the basic theory behind PARACEST contrast agents, their benefits over other contrast agents and their applications to MRI. It then describes some of the recent PARACEST research results: specifically, pH measurements using water molecule exchange rate modulation, T2 exchange contrast caused by water molecule exchange, the use of ultrashort TEs (TE < 10 µs) to overcome T2 exchange line broadening and the potential application of T2 exchange as a new contrast mechanism for MRI.

  3. Removal of thiosulfates from return waters by ion exchange

    SciTech Connect

    Parkhomovskii, V.L.; Kryzhandvskii, M.M.; Savva, V.P.; Timofeeva, I.V.

    1986-08-01

    The authors select an anion-exchange resin and its ionic form having high exchange capacity for thiosulfate, from which the sorbed thiosulfate ions can be effectively desorbed. Three types of strongly basic anion-exchangers were used: AV-17; AV-1710P; AV-29-10P. The experimental results showed that all three aninon-exchangers had approximately the same capacity for thiosulfate ions. Curves representing sorption and regeneration during purification of model solutions are show. The resins were regenerated under dynamic conditions by 1 N sodium sulfate solution. The degree of regeneration was 95%.

  4. Tc-99 Ion Exchange Resin Testing

    SciTech Connect

    Valenta, Michelle M.; Parker, Kent E.; Pierce, Eric M.

    2010-08-01

    Pacific Northwest National Laboratory was contracted by CHPRC to evaluate the release of 99Tc from spent resin used to treat water from well 299-W15-765 and stored for several years. The key questions to be answered are: 1) does 99Tc readily release from the spent ion exchange resin after being in storage for several years; 2) if hot water stripping is used to remove the co-contaminant carbon tetrachloride, will 99Tc that has been sequestered by the resin be released; and 3) can spent resin be encapsulated into a cementitious waste form; if so, how much 99Tc would be released from the weathering of the monolith waste form? The results from the long term stability leach test results confirm that the resin is not releasing a significant amount of the sequestered 99Tc, evident by the less than 0.02% of the total 99Tc loaded being identified in the solution. Furthermore, it is possible that the measured 99Tc concentration is the result of 99Tc contained in the pore spaces of the resin. In addition to these results, analyses conducted to examine the impact of hot water on the release of 99Tc suggest that only a small percentage of the total is being released. This suggest that hot water stripping to remove carbon tetrachloride will not have a significant affect on the resin’s ability to hold-on to sequestered 99Tc. Finally, encapsulation of spent resin in a cementitious material may be a viable disposal option, but additional tests are needed to examine the extent of physical degradation caused by moisture loss and the effect this degradation process can have on the release of 99Tc.

  5. Enhanced DOC removal using anion and cation ion exchange resins.

    PubMed

    Arias-Paic, Miguel; Cawley, Kaelin M; Byg, Steve; Rosario-Ortiz, Fernando L

    2016-01-01

    Hardness and DOC removal in a single ion exchange unit operation allows for less infrastructure, is advantageous for process operation and depending on the water source, could enhance anion exchange resin removal of dissolved organic carbon (DOC). Simultaneous application of cationic (Plus) and anionic (MIEX) ion exchange resin in a single contact vessel was tested at pilot and bench scales, under multiple regeneration cycles. Hardness removal correlated with theoretical predictions; where measured hardness was between 88 and 98% of the predicted value. Comparing bench scale DOC removal of solely treating water with MIEX compared to Plus and MIEX treated water showed an enhanced DOC removal, where removal was increased from 0.5 to 1.25 mg/L for the simultaneous resin application compared to solely applying MIEX resin. A full scale MIEX treatment plant (14.5 MGD) reduced raw water DOC from 13.7 mg/L to 4.90 mg/L in the treated effluent at a bed volume (BV) treatment rate of 800, where a parallel operation of a simultaneous MIEX and Plus resin pilot (10 gpm) measured effluent DOC concentrations of no greater than 3.4 mg/L, even at bed volumes of treatment 37.5% greater than the full scale plant. MIEX effluent compared to simultaneous Plus and MIEX effluent resulted in differences in fluorescence intensity that correlated to decreases in DOC concentration. The simultaneous treatment of Plus and MIEX resin produced water with predominantly microbial character, indicating the enhanced DOC removal was principally due to increased removal of terrestrially derived organic matter. The addition of Plus resin to a process train with MIEX resin allows for one treatment process to remove both DOC and hardness, where a single brine waste stream can be sent to sewer at a full-scale plant, completely removing lime chemical addition and sludge waste disposal for precipitative softening processes.

  6. Hydrogen/deuterium exchange of myoglobin ions in a linear quadrupole ion trap.

    PubMed

    Mao, Dunmin; Ding, Chuanfan; Douglas, D J

    2002-01-01

    The hydrogen/deuterium (H/D) exchange of gas-phase ions of holo- and apo-myoglobin has been studied by confining the ions in a linear quadrupole ion trap with D(2)O or CD(3)OD at a pressure of several mTorr. Apo-myoglobin ions were formed by collision-induced dissociation of holo-myoglobin ions between the orifice and skimmer of the ion sampling system. The exchange takes place on a time scale of seconds. Earlier cross section measurements have shown that holo-myoglobin ions can have more compact structures than apo-myoglobin. Despite this, both holo-myoglobin and apo-myoglobin in charge states +8 to +14 are found to exchange nearly the same number of hydrogens (ca. 103) in 4 s. It is possible the ions fold or unfold to new conformations on the much longer time scale of the exchange experiment compared with the cross section measurements.

  7. Interpenetrating polymer network ion exchange membranes and method for preparing same

    DOEpatents

    Alexandratos, Spiro D.; Danesi, Pier R.; Horwitz, E. Philip

    1989-01-01

    Interpenetrating polymer network ion exchange membranes include a microporous polymeric support film interpenetrated by an ion exchange polymer and are produced by absorbing and polymerizing monomers within the support film. The ion exchange polymer provides ion exchange ligands at the surface of and throughout the support film which have sufficient ligand mobility to extract and transport ions across the membrane.

  8. XAFS Studies of Silver Environments in Ion-Exchanged Glasses

    SciTech Connect

    Yang, X. C.; Dubiel, M.

    2007-02-02

    The X-ray absorption fine structure (XAFS) technique was used to analyze the structural geometry of Ag atoms introduced into soda-lime silicate glass and soda aluminosilicate glass by ion-exchange methods. The results show that Ag+ ions in aluminosilicate glass are coordinated by about two oxygens and the nearest-neighbor Ag-O distance increases when the Ag+-for-Na+ ion-exchange ratio is larger than 0.47. When the exchange ratio is low, the introduced Ag+ ions are stabilized at the non-bridge oxygen (NBO) site with a Ag-O distance of 2.20 A, and the Na+ ions in the AlO4 site are exchanged by Ag+ ions after full replacement of the NBO sites with a Ag-O distance of 2.28 A. The disorder of Ag-O coordination increases with increasing ion-exchange ratio in aluminosilicate glass where Ag+ ions are coordinated by NBO and bridge oxygen (BO)

  9. Ion Exchange Separation of the Oxidation State of Vanadium.

    ERIC Educational Resources Information Center

    Cornelius, Richard

    1980-01-01

    Describes an experiment that emphasizes the discrete nature of the different oxidation states of vanadium by the separation of ammonium metavanadate into all four species by ion exchange chromatography. (CS)

  10. Ion Exchanged, Glass Laminates that Exhibit a Threshold Strength

    DTIC Science & Technology

    2006-07-10

    tests. The glass was then annealed at 550 ’C for 8hr to remove any residual stress. The ion exchange process was accomplished in a vertical clam ...bonded together (described below) before the ion exchange. Hence, when the bilayer plate was separated using a razor blade (described below), each...strain energy release rate for the bonded interface using the double cantilever beam test configuration. As detailed by Maszara et. al., 19 a razor blade

  11. Semi-aerobic stabilized landfill leachate treatment by ion exchange resin: isotherm and kinetic study

    NASA Astrophysics Data System (ADS)

    Zamri, Mohd Faiz Muaz Ahmad; Kamaruddin, Mohamad Anuar; Yusoff, Mohd Suffian; Aziz, Hamidi Abdul; Foo, Keng Yuen

    2015-03-01

    This study was carried out to investigate the treatability of ion exchange resin (Indion MB 6 SR) for the removal of chromium (VI), aluminium (III), zinc (II), copper (II), iron (II), and phosphate (PO4)3-, chemical oxygen demand (COD), ammonia nitrogen (NH3-N) and colour from semi-aerobic stabilized leachate by batch test. A range of ion exchange resin dosage was tested towards the removal efficiency of leachate parameters. It was observed that equilibrium data were best represented by the Langmuir model for metal ions and Freundlich was ideally fit for COD, NH3-N and colour. Intra particle diffusion model, pseudo first-order and pseudo second-order isotherm models were found ideally fit with correlation of the experimental data. The findings revealed that the models could describe the ion exchange kinetic behaviour efficiently, which further suggests comprehensive outlook for the future research in this field.

  12. Samarium Ion Exchanged Montmorillonite for High Temperature Cumene Cracking Reaction

    NASA Astrophysics Data System (ADS)

    Binitha, N. N.; Silija, P. P.; Suraj, V.; Yaakob, Z.; Sugunan, S.

    2011-02-01

    Montmorillonite clay is cation exchanged with samarium and its catalytic influence in cumene cracking reaction is investigated. Effect of exchange with sodium ions on further exchange with samarium ions is also noted. Acidity measurements are done using Temperature Programmed Desorption (TPD) of ammonia. The retention of basic structure is proved from FTIR spectra and XRD patterns. Elemental analysis result shows that samarium exchange has occurred, which is responsible for the higher catalytic activity. Surface area and pore volume remains more or less unaffected upon exchange. Thermogravimetric analysis indicates the enhanced thermal stability on exchanging. Cumene cracking reaction is carried out at atmospheric pressure in a fixed bed glass reactor at 673 K. The predominance of Brønsted acidity is confirmed from high selectivity to benzene.

  13. Partition Coefficients of Selected Compounds Using Ion Exchange Separation of Cesium From High Level Waste

    SciTech Connect

    Toth, James J.; Blanchard, David L.; Arm, Stuart T.; Urie, Michael W.

    2004-04-24

    The removal of cesium radioisotope (137Cs) from the High Level Waste stored in underground storage tanks at the Hanford site is a formidable chemical separations challenge for the Waste Treatment Plant. An eluatable organic-based ion exchange resin was selected as the baseline technology (1). The baseline technology design employs a proprietary macrocyclic weak-acid ion exchange resin to adsorb the cesium (137Cs) during the process loading cycle in a fixed bed column design. Following loading, the cesium is eluted from the resin using a nitric acid eluant. Previous work provided limited understanding of the performance of the resin, processed with actual wastes, and under multiple load and elute conditions, which are required for the ion exchange technology to be underpinned sufficiently for resolution of all process-related design issues before flowsheet and construction drawings can be released. By performing multiple ion exchange column tests with waste feeds, and measuring the chemical and radionuclide compositions of the waste feeds, column effluents and column eluants, ion exchange stream composition information can be provided for supporting resolution of selected design issues.

  14. Anion selective membrane. [ion exchange resins and ion exchange membrane electrolytes for electrolytic cells

    NASA Technical Reports Server (NTRS)

    Alexander, S. S.; Geoffroy, R. R.; Hodgdon, R. B.

    1975-01-01

    Experimental anion permselective membranes were prepared and tested for their suitability as cell separators in a chemical redox power storage system being developed at NASA-Lewis Research Center. The goals of long-term (1000 hr) oxidative and thermal stability at 80 C in FeCl3 and CrCl3 electrolytes were met by most of the weak base and strong base amino exchange groups considered in the program. Good stability is exhibited by several of the membrane substrate resins. These are 'styrene' divinylbenzene copolymer and PVC film. At least four membrane systems produce strong flexible films with electrochemical properties (resistivity, cation transfer) superior to those of the 103QZL, the most promising commercial membrane. The physical and chemical properties of the resins are listed.

  15. Speciation of Trace Di- and Triorganotins in Water by Ion Exchange HPLC-GFAA.

    DTIC Science & Technology

    1980-08-05

    automated slement- specific detectors for high prssure liquid chromatography (iPLC): the determination of arsenite, arsenate, methylarsonic acid, arid...Furnace Atomic Absorption, High -Pressure Liquid Chromatography , Ion Exchange, Leaching, Nanogram Sensitivityk Organotin Cations, Speciation, Triorganoti n...organosiloxanea offers nearly unlimited applications for high performance liquid chromatography . Not only do such chemically bonded column packings resist a

  16. Ion momentum and energy transfer rates for charge exchange collisions

    NASA Technical Reports Server (NTRS)

    Horwitz, J.; Banks, P. M.

    1973-01-01

    The rates of momentum and energy transfer have been obtained for charge exchange collisions between ion and neutral gases having arbitrary Maxwellian temperatures and bulk transport velocities. The results are directly applicable to the F-region of the ionosphere where 0+ - 0 charge is the dominant mechanism affecting ion momentum and energy transfer.

  17. ELUTION OF URANIUM VALUES FROM ION EXCHANGE RESINS

    DOEpatents

    Kennedy, R.H.

    1959-11-24

    A process is described for eluting complex uranium ions absorbed on ion exchange resins. The resin is subjected to the action of an aqueous eluting solution contuining sulfuric acid and an alkali metal, ammonium, or magnesium chloride or nitrate, the elution being carried out until the desired amount of the uranium is removed from the resin.

  18. Microsecond pulsed hydrogen/deuterium exchange of electrosprayed ubiquitin ions stored in a linear ion trap.

    PubMed

    Rajabi, Khadijeh

    2015-02-07

    A pulse of D2O vapour on the order of microseconds is allowed to react with the +6 to +9 charge states of ubiquitin confined in a linear ion trap (LIT). Two envelopes of peaks are detected for the ions of ubiquitin, corresponding to the ions that exchange more quickly and more slowly. The deuterium uptake of the protonated sites on ubiquitin ions accounts for the ion population with the fast exchange. The hydrogen/deuterium exchange (HDX) kinetics of ubiquitin ions trapped in the LIT for 200 ms showed comparable structural transitions to those trapped for 300 ms. When ions are trapped for longer, i.e. up to 2000 ms, mainly the slow exchanging ion population is detected. In all experiments the +7 ions exchange the most, suggesting a short distance between the surface protonated sites and nearby charged sites, and concomitantly high accessibility of surface protonated sites towards D2O. The +6 ions are more compact than the +7 ions but have one fewer protonated site, therefore fewer surface availabilities for D2O attack. The data suggest that the +6 ions keep most of their solution-phase contacts intact while the hydrophobic core is slightly interrupted in the +7 ions, possibly due to the exposure of charged His68 that is normally buried in the hydrophobic pocket. The +8 and +9 ions have more protonated sites but are less compact than the +7 ions because of Coulombic repulsion, resulting in a larger distance between the protonated sites and the basic sites. The data indicate that the HDX mechanism of ions with the slower exchange corresponding to the second envelope of peaks is primarily governed via a relay mechanism. The results suggest that the pulsed HDX MS method is sampling a population of ubiquitin ions with a similar backbone fold to the solution.

  19. Desalination of brackish waters using ion-exchange media

    SciTech Connect

    Pless, J.D.; Philips, M.L.F.; Voigt, J.A.; Moore, D.; Axness, M.; Krumhansl, J.L.; Nenoff, T.M.

    2006-06-21

    An environmentally friendly method and materials study for desalinating inland brackish waters (i.e., coal bed methane produced waters) using a set of ion-exchange materials is presented. This desalination process effectively removes anions and cations in separate steps with minimal caustic waste generation. The anion-exchange material, hydrotalcite (HTC), exhibits an ion-exchange capacity (IEC) of around 3 mequiv g{sup -1}. The cation-exchange material, an amorphous aluminosilicate permutite-like material, (Na{sub x}+2yAl{sub x}Si{sub 1}-xO{sub 2+y}), has an IEC of around to 2.5 mequiv g{sup -1}. These ion-exchange materials were studied and optimized because of their specific ion-exchange capacity for the ions of interest and their ability to function in the temperature and pH regions necessary for cost and energy effectiveness. Room temperature, minimum pressure column studies (once-pass through) on simulant brackish water (total dissolved solids (TDS) = 2222 ppm) resulted in water containing TDS = 25 ppm. A second once-pass through column study on actual produced water (TDS = similar to 11 000) with a high carbonate concentration used an additional lime softening step and resulted in a decreased TDS of 600 ppm.

  20. Desalination of brackish waters using ion exchange media.

    SciTech Connect

    Pless, Jason D.; Krumhansl, James Lee; Nenoff, Tina Maria; Voigt, James A.; Phillips, Mark L. F.; Axness, Marlene; Moore, Diana Lynn

    2005-01-01

    An environmentally friendly method and materials study for desalinating inland brackish waters (i.e., coal bed methane produced waters) using a set of ion-exchange materials is presented. This desalination process effectively removes anions and cations in separate steps with minimal caustic waste generation. The anion-exchange material, hydrotalcite (HTC), exhibits an ion-exchange capacity (IEC) of {approx} 3 mequiv g{sup -1}. The cation-exchange material, an amorphous aluminosilicate permutite-like material, (Na{sub x+2y}Al{sub x}Si{sub 1-x}O{sub 2+y}), has an IEC of {approx}2.5 mequiv g{sup -1}. These ion-exchange materials were studied and optimized because of their specific ion-exchange capacity for the ions of interest and their ability to function in the temperature and pH regions necessary for cost and energy effectiveness. Room temperature, minimum pressure column studies (once-pass through) on simulant brackish water (total dissolved solids (TDS) = 2222 ppm) resulted in water containing TDS = 25 ppm. A second once-pass through column study on actual produced water (TDS = {approx}11,000) with a high carbonate concentration used an additional lime softening step and resulted in a decreased TDS of 600 ppm.

  1. Rate theory on water exchange in aqueous uranyl ion

    NASA Astrophysics Data System (ADS)

    Dang, Liem X.; Vo, Quynh N.; Nilsson, Mikael; Nguyen, Hung D.

    2017-03-01

    We report a classical rate theory approach to predict the exchange mechanism that occurs between water and aqueous uranyl ion. Using our water and ion-water polarizable force field and molecular dynamics techniques, we computed the potentials of mean force for the uranyl ion-water pair as a function of different pressures at ambient temperature. These potentials of mean force were used to calculate rate constants using transition rate theory; the transmission coefficients also were examined using the reactive flux method and Grote-Hynes approach. The computed activation volumes are positive; thus, the mechanism of this particular water-exchange is a dissociative process.

  2. Exchange and reduction of Cu(2+) ions in clinoptilolite.

    PubMed

    Iznaga, I Rodríguez; Petranovskii, V; Fuentes, G Rodríguez; Mendoza, C; Aguilar, A Benítez

    2007-12-15

    The ion-exchange and reduction processes for Cu(2+) ions in clinoptilolite from the Caimanes deposit (Moa, Cuba) were studied at different temperatures. The ion-exchange studies were done to determine the kinetic parameters of Cu(2+) removal from solution by this clinoptilolite modified previously to NH(+)(4) form, and thermodynamic parameters of Cu(2+) elution from zeolite using NH(4)Cl solution. The results show that temperature increase favors the exchange and that it is a reversible process. The external diffusion rate appreciably increases with temperature, while, the internal diffusion coefficient rises relatively little. This means that besides ion exchange other processes (such as precipitation of the low-solubility phase and/or salt adsorption) occur, which cause copper removal from solution and affect the intracrystalline diffusion of the ions. For steric reasons the exchange of [Cu(H(2)O)(6)](2+) ions from a solution must occur with a number of water molecules n smaller than 6 (6 > n > or = 0). Cu(2+) reduction by hydrogen and the formation of Cu-particles in the clinoptilolite were verified. The Cu(2+) reduction mechanism is complex, indirect, and sensitive to reduction temperature; consequently, Cu(+)(n) states intermediate between Cu(2+) and Cu(0) should be present in the reduced samples.

  3. Electrical and magnetic properties of ion-exchangeable layered ruthenates

    SciTech Connect

    Sugimoto, Wataru . E-mail: wsugi@shinshu-u.ac.jp; Omoto, Masashi; Yokoshima, Katsunori; Murakami, Yasushi; Takasu, Yoshio

    2004-12-01

    An ion-exchangeable ruthenate with a layered structure, K{sub 0.2}RuO{sub 2.1}, was prepared by solid-state reactions. The interlayer cation was exchanged with H{sup +}, C{sub 2}H{sub 5}NH{sub 3}{sup +}, and ((C{sub 4}H{sub 9}){sub 4}N{sup +}) through proton-exchange, ion-exchange, and guest-exchange reactions. The electrical and magnetic properties of the products were characterized by DC resistivity and susceptibility measurements. Layered K{sub 0.2}RuO{sub 2.1} exhibited metallic conduction between 300 and 13K. The products exhibited similar magnetic behavior despite the differences in the type of interlayer cation, suggesting that the ruthenate sheet in the protonated form and the intercalation compounds possesses metallic nature.

  4. Quantitative ion-exchange separation of plutonium from impurities

    SciTech Connect

    Pietri, C.E.; Freeman, B.P.; Weiss, J.R.

    1981-09-01

    The methods used at the New Brunswick Laboratory for the quantitative ion exchange separation of plutonium from impurities prior to plutonium assay are described. Other ion exchange separation procedures for impurity determination and for isotopic abundance measurements are given. The primary technique used consists of sorption of plutonium(IV) in 8N HNO/sub 3/ on Dowex-1 anion exchange resin and elution of the purified plutonium with 0.3N HCl-0.01N HF. Other methods consist of the anion exchange separation of plutonium(IV) in 12N HCl and the cation exchange separation of plutonium(III) in 0.2 N HNO/sub 3/. The application of these procedures to the subsequent assay of plutonium, isotopic analysis, and impurity determination is described.

  5. Ion-exchange chromatographic analysis of peroxynitric acid.

    PubMed

    Nakashima, Yoichi; Ikawa, Satoshi; Tani, Atsushi; Kitano, Katsuhisa

    2016-01-29

    Ion-exchange chromatographic analysis of peroxynitric acid (O2NOOH) was performed by combining an acidic eluate with an UV-vis detector and immersing the separation column in an ice-water bath. The decomposition behavior of peroxynitric acid in the solution was also studied using this system. The fraction for the peroxynitric acid peak was collected. Ion-exchange chromatographic analysis of this fraction, after standing at room temperature for 24h, showed that the decomposition products were mainly nitrate ions with a very small amount of nitrous acid. The peroxynitric acid peak area correlated perfectly with the total amount of decomposition products. The ion-exchange chromatographic isolation allowed us to evaluate the molar extinction coefficient of peroxynitric acid precisely in a wider wavelength range than previous reports. The value decreases monotonically from 1729±26M(-1)cm(-1) at 200nm to 12.0±0.5M(-1)cm(-1) at 290nm.

  6. H/D exchange of gas phase bradykinin ions in a linear quadrupole ion trap.

    PubMed

    Mao, Dunmin; Douglas, D J

    2003-02-01

    The gas phase H/D exchange reaction of bradykinin ions, as well as fragment ions of bradykinin generated through collisions in an orifice skimmer region, have been studied with a linear quadrupole ion trap (LIT) reflectron time-of-flight (rTOF) mass spectrometer system. The reaction in the trap takes only tens of seconds at a pressure of few mTorr of D2O or CD3OD. The exchange rate and hydrogen exchange level are not sensitive to the trapping q value over a broad range, provided q is not close to the stability boundary (q = 0.908). The relative rates and hydrogen exchange levels of protonated and sodiated +1 and +2 ions are similar to those observed previously by others with a Fourier transform ion cyclotron resonance (FTICR) mass spectrometer system. The doubly and triply protonated ions show multimodal isotopic distributions, suggesting the presence of several different conformations. The y fragment ions show greater exchange rates and levels than a or b ions, and when water or ammonia is lost from the fragment ions, no exchange is observed.

  7. In Situ Investigations of Ion Exchange Processes in Microporous Materials

    NASA Astrophysics Data System (ADS)

    Lee, Y.; Parise, J. B.; Hanson, J. C.

    2001-12-01

    The mechanism by which ions exchange in microporous and layered solids, such as zeolites and clays for example, has important implications in areas as diverse as soil fertility and environmental remediation. A detailed characterization of the ion-exchange pathway, the structural consequences of ion exchange and the specific sites involved in the course of exchange, is desirable. A probe that is both time- and structure-sensitive allows resolution of which specific sites are involved, along with the effects of different cation types on the uptake and release of ions. In order to discern the mechanism of ion exchange, it is necessary not only to observe the course of the reaction, which can now be done routinely using energy dispersive X-ray diffraction at synchrotron sources, but also to collect dynamic diffraction data of sufficient quality to allow structure refinement using Rietveld structure refinement techniques. This at present requires the collection of monochromatic data. Tradeoffs between time-resolution, peak-to-background discrimination and structural resolution are often required and depend on the problem at hand. We have developed a number of strategies for in situ ion exchange techniques that probe both structural and kinetic information from dynamic solid media. Examples include investigations of the site-specific ion-exchange mechanism in zeolite LSX using a combination of ex situ and in situ time-resolved synchrotron X-ray powder diffraction, Iterative Target Transformation Factor Analysis (ITTFA) and Rietveld structural refinements. Measurement of competitive ion depletion curves showed that the newly synthesized gallosilicate TsG-1 is more selective for Sr than mineral clinoptilolite, and the structural pathway of Sr-exchange in TsG-1 was monitored by in situ and ex situ synchrotron X-ray powder diffraction. In those cases where full structure refinement is desirable using less than optimal powder diffraction data, we found it necessary to first

  8. Properties of a Novel Ion-Exchange Film

    NASA Technical Reports Server (NTRS)

    Street, Kenneth W.; Hill, Carol M.; Philipp, Warren H.; Tanner, Stephen P.; Gorse, Joseph; Lusk, Amy; Taylor, Jason; Dickens, Jason

    2004-01-01

    A new ion-exchange material (based on polyacrylic acid) and some of its analytical applications have been reported. This paper contains data on the ion-exchange properties of the film form of the material and its potential application to the decontamination of waste water and drinking water. The film has a high exchange capacity of 5 to 6 meq/g and a pK(sub a) of 5.7. The calcium form is the most effective for removing metal ions from solution, and the optimum pH range is between 5 and 7. The exchange rates are slower for the film than for bead and powder forms of the ion-exchange material; otherwise, the properties are similar. The film is effective when hard water solutions are employed and also when metal ions are in the complex matrix of waste water from electroplating. The film can be used in flow systems having a flow channel large enough to allow passage of turbid solutions.

  9. Properties of a Novel Ion-Exchange Film

    NASA Technical Reports Server (NTRS)

    Street, Kenneth W.; Hill, Carol M.; Philipp, Warren H.; Tanner, Stephen P.; Gorse, Joseph; Lusk, Amy; Taylor, Jason; Dickens, Jason

    2002-01-01

    A new ion-exchange material (based on polyacrylic acid) and some of its analytical applications have been reported. This paper contains data on the ion-exchange properties of the film form of the material and its potential application to the decontamination of waste water and drinking water. The film has a high exchange capacity of 5 to 6 meq/g and a pK(sub a) of 5.7. The calcium form is the most effective for removing metal ions from solution, and the optimum pH range is between 5 and 7. The exchange rates are slower for the film than for bead and powder forms of the ion-exchange material; otherwise, the properties are similar. The film is effective when hard water solutions are employed and also when metal ions are in the complex matrix of waste water from electroplating. The film can be used in flow systems having a flow channel large enough to allow passage of turbid solutions.

  10. Cementation of residue ion exchange resins at Rocky Flats

    SciTech Connect

    Dustin, D.F.; Beckman, T.D.; Madore, C.M.

    1998-03-03

    Ion exchange resins have been used to purify nitric acid solutions of plutonium at Rocky Flats since the 1950s. Spent ion exchange resins were retained for eventual recovery of residual plutonium, typically by incineration followed by the aqueous extraction of plutonium from the resultant ash. The elimination of incineration as a recovery process in the late 1980s and the absence of a suitable alternative process for plutonium recovery from resins led to a situation where spent ion exchange resins were simply placed into temporary storage. This report describes the method that Rocky Flats is currently using to stabilize residue ion exchange resins. The objective of the resin stabilization program is: (1) to ensure their safety during interim storage at the site, and (2) to prepare them for ultimate shipment to the Waste Isolation Pilot Plant (WIPP) in New Mexico. Included in the discussion is a description of the safety concerns associated with ion exchange resins, alternatives considered for their stabilization, the selection of the preferred treatment method, the means of implementing the preferred option, and the progress to date.

  11. Ion exchange in KTiOPO4 crystals irradiated by copper and hydrogen ions.

    PubMed

    Zhang, Ruifeng; Lu, Fei; Lian, Jie; Liu, Hanping; Liu, Xiangzhi; Lu, Qingming; Ma, Hongji

    2008-05-12

    Cs(+)-K+ ion exchanges were produced on KTiOPO4 crystals which is prior irradiated by Cu+ can H+ ions. The energy and dose of implanted Cu+ ions are 1.5 MeV and 0.5 x 10(14) ions/cm2, and that of H+ are 300 keV and 1 x 10(16) ions/cm2, respectively. The temperature of ions exchange is 430 degrees C, and the time range from 15 minutes to 30 minutes. The prism coupling method is used to measure the dark mode spectra of the samples. Compared with results of ion exchange on the sample without irradiations, both the number of guided mode and its corresponding effective refractive index are decreased. The experimental results indicate that the ion exchange rate closely related with the lattice damage and the damage layers formed in the depth of maximum nuclear energy deposition act as a barrier to block the ions diffuse into the sample and the concentration of defects can modify the speed of ion exchange..

  12. The electrochemical investigation of salts partition with ion exchange membranes.

    PubMed

    Ata, Nejla; Yazicigil, Zafer; Oztekin, Yasemin

    2008-12-15

    The regenaration of acid and base from the solutions containing metallic salts was achieved by salt splitting method (SSM) using not only anion-exchange membranes (AEM) but also cation-exchange membrane (CEM). In these experiments, while the ion exchange membrane was anion-exchange membrane, acid solutions were used as an anolyte and different salts of potassium were used as a catholyte. In addition to these experiments, while the ion exchange membrane was cation-exchange membrane, base solutions were used as a catholyte and different salts of potassium were used as an anolyte. The effects of current density, initial concentrations of anolyte and catholyte solutions, the type of salt solution and the type of the ion-exchange membranes on the recovery ratio of bases and acids were investigated. The results of the experiments were investigated with the Statistical Package for Social Sciences (SPSS) program. The obtained results show that this technique can be used not only for recovering the acid and base wastes of industry but also for removing the impurities in order to obtain pure acids and bases in laboratory conditions.

  13. Ion exchange polymers for anion separations

    DOEpatents

    Jarvinen, Gordon D.; Marsh, S. Fredric; Bartsch, Richard A.

    1997-01-01

    Anion exchange resins including at least two positively charged sites and a ell-defined spacing between the positive sites are provided together with a process of removing anions or anionic metal complexes from aqueous solutions by use of such resins. The resins can be substituted poly(vinylpyridine) and substituted polystyrene.

  14. Ion exchange polymers for anion separations

    DOEpatents

    Jarvinen, G.D.; Marsh, S.F.; Bartsch, R.A.

    1997-09-23

    Anion exchange resins including at least two positively charged sites and a well-defined spacing between the positive sites are provided together with a process of removing anions or anionic metal complexes from aqueous solutions by use of such resins. The resins can be substituted poly(vinylpyridine) and substituted polystyrene.

  15. THERMODYNAMICS OF ION-EXCHANGED NATURAL CLINOPTILOLITE

    EPA Science Inventory

    Natural clinoptilolite from Castle Creek, Idaho, and its cation-exchanged variants (Na-Cpt, NaK-Cpt, K-Cpt, and Ca-Cpt) were studied by high-temperature calorimetry. The hydration enthalpy for all clinoptilolites is about -30 kJ/mol H2O (liquid water reference state) at 25 C. T...

  16. Development and evaluation of ion exchange hollow fibers. [vinyl copolymers

    NASA Technical Reports Server (NTRS)

    Smith, J. K.

    1975-01-01

    An ion exchange hollow fiber impregnated with a vinylpyridine base was developed. The basic exchange resin used to impart the necessary permselectivity to the hollow fiber is a copolymer of vinylpyridine and dibromoethane prepared according to Rembaum. A slight pressure was used to impregnate the exchange monomer mixture into the void structure of the fiber wall, and with maintenance of subambient temperatures, the rate of cross-linking is slow enough to allow the growing polymer to permeate the wall structure before significant increase in polymer molecular weight. These ion exchange fibers are produced from polyacrylonitrile hollow fibers with an appropriate wall structure that enables the impregnating vinylpyridine monomer mixture to form a truly semipermeable anion barrier after curing.

  17. ION EXCHANGE IN FUSED SALTS. IV. DISTRIBUTION OF SELECTED TRANSITION ELEMENTS IN THE CHABAZITE-MOLTEN NANO3 SYSTEM,

    DTIC Science & Technology

    MINERALS, ION EXCHANGE, ION EXCHANGE, FUEL CELLS, LANTHANUM, DECOMPOSITION, EUROPIUM, IONS, EQUILIBRIUM(PHYSIOLOGY), NITRATES, COBALT, DISTRIBUTION, CERIUM, SILICATES, TRANSITION METALS, MOLTEN SALT NUCLEAR REACTORS.

  18. Recovery of boric acid from ion exchangers

    DOEpatents

    Pollock, Charles W.

    1976-01-01

    The recovery of boric acid from an anion exchange resin is improved by eluting the boric acid with an aqueous solution of ammonium bicarbonate. The boric acid can be readily purified and concentrated by distilling off the water and ammonium bicarbonate. This process is especially useful for the recovery of boric acid containing a high percentage of .sup.10 B which may be found in some nuclear reactor coolant solutions.

  19. Catalysis using hydrous metal oxide ion exchangers

    DOEpatents

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

    1983-07-21

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

  20. Catalysis using hydrous metal oxide ion exchanges

    DOEpatents

    Dosch, Robert G.; Stephens, Howard P.; Stohl, Frances V.

    1985-01-01

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

  1. Charge-exchange plasma generated by an ion thruster

    NASA Technical Reports Server (NTRS)

    Kaufman, H. R.

    1977-01-01

    The charge exchange plasma generated by an ion thruster was investigated experimentally using both 5 cm and 15 cm thrusters. Results are shown for wide ranges of radial distance from the thruster and angle from the beam direction. Considerations of test environment, as well as distance from the thruster, indicate that a valid simulation of a thruster on a spacecraft was obtained. A calculation procedure and a sample calculation of charge exchange plasma density and saturation electron current density are included.

  2. Spin-locking versus chemical exchange saturation transfer MRI for investigating chemical exchange process between water and labile metabolite protons.

    PubMed

    Jin, Tao; Autio, Joonas; Obata, Takayuki; Kim, Seong-Gi

    2011-05-01

    Chemical exchange saturation transfer (CEST) and spin-locking (SL) experiments were both able to probe the exchange process between protons of nonequivalent chemical environments. To compare the characteristics of the CEST and SL approaches in the study of chemical exchange effects, we performed CEST and SL experiments at varied pH and concentrated metabolite phantoms with exchangeable amide, amine, and hydroxyl protons at 9.4 T. Our results show that: (i) on-resonance SL is most sensitive to chemical exchanges in the intermediate-exchange regime and is able to detect hydroxyl and amine protons on a millimolar concentration scale. Off-resonance SL and CEST approaches are sensitive to slow-exchanging protons when an optimal SL or saturation pulse power matches the exchanging rate, respectively. (ii) Offset frequency-dependent SL and CEST spectra are very similar and can be explained well with an SL model recently developed by Trott and Palmer (J Magn Reson 2002;154:157-160). (iii) The exchange rate and population of metabolite protons can be determined from offset-dependent SL or CEST spectra or from on-resonance SL relaxation dispersion measurements. (iv) The asymmetry of the magnetization transfer ratio (MTR(asym)) is highly dependent on the choice of saturation pulse power. In the intermediate-exchange regime, MTR(asym) becomes complicated and should be interpreted with care.

  3. Polymer useful for an ion exchange membrane

    DOEpatents

    Liang, Siwei; Lynd, Nathaniel A.

    2017-03-14

    The present invention provides for a polymer formed by reacting a first reactant polymer, or a mixture of first reactant polymers comprising different chemical structures, comprising a substituent comprising two or more nitrogen atoms (or a functional group/sidechain comprising a two or more nitrogen atoms) with a second reactant polymer, or a mixture of second reactant polymers comprising different chemical structures, comprising a halogen substituent (or a functional group/sidechain comprising a halogen).

  4. Bench-Scale Studies with Argentine Ion Exchange Material

    SciTech Connect

    Cicero-Herman, C.A.

    2002-06-28

    The United States Department of Energy (DOE), as well as international atomic energy commission, facilities use ion exchange materials for purification of aqueous streams in the nuclear industry. Unfortunately, the use of the ion exchange materials creates a waste stream that can be very high in both organic and radioactive constituents. Therefore, disposal of the spent resins often becomes an economic problem because of the large volumes of resin produced and the relatively few technologies that are capable of economically stabilizing this waste. Vitrification of this waste stream presents a reasonable disposable alternative because of its inherent destruction capabilities, the volume reductions obtainable, and the durable product that it produces.

  5. Rupture loop annex ion exchange RLAIX vault deactivation

    SciTech Connect

    Ham, J.E.; Harris, D.L., Westinghouse Hanford

    1996-08-01

    This engineering report documents the deactivation, stabilization and final conditions of the Rupture Loop Annex Ion Exchange (RLAIX) Vault located northwest of the 309 Building`s Plutonium Recycle Test Reactor (PRTR). Twelve ion exchange columns, piping debris, and column liquid were removed from the vault, packaged and shipped for disposal. The vault walls and floor were decontaminated, and portions of the vault were painted to fix loose contamination. Process piping and drains were plugged, and the cover blocks and rain cover were installed. Upon closure,the vault was empty, stabilized, isolated.

  6. Ion exchange chromatography of proteins and clearance of aggregates.

    PubMed

    Yigzaw, Y; Hinckley, P; Hewig, A; Vedantham, G

    2009-06-01

    Clearance of product related aggregates in therapeutic proteins is a major focus of purification process development. A typical purification process will have one or two chromatographic steps that remove these product related aggregates to an acceptable level. Both cation exchange and anion exchange chromatography can provide robust clearance of aggregates. The primary factors that are critical for aggregate clearance are: resin chemistry, binding and elution condition, peak collection and column load factor. This review covers how these factors can be optimized to increase the effectiveness of ion exchange chromatography in removing aggregates.

  7. Theorization on ion-exchange equilibria: activity of species in 2-D phases.

    PubMed

    Tamura, Hiroki

    2004-11-01

    Ion-exchange reactions are naturally occurring at soil and sediment/water interphases, determining soil fertility and water quality. These ion-exchange reactions with inorganic and organic exchangers are applied to chemical analysis, recovery of useful ions from low-grade ores (potentially from sea water), water purification including the preparation of "ultrapure" water, production of foods and medicines, therapy, and other uses. It is important to theorize about or to model ion-exchange reactions for quantitative explanations of ion-exchange phenomena and for efficient operation of ion-exchange processes. This paper describes the modeling of ion-exchange equilibria for hydroxyl sites on metal oxides and carboxyl sites in resins with monovalent cations (alkali metal ions), a monovalent anion (nitrate ion), and divalent heavy metal ions. The procedure of modeling is as follows: the stoichiometry and material balance equations of the respective ion-exchange reactions were established based on findings here and by others. The equilibrium conditions were given by the Frumkin equation, where the mass-action relation is modified with lateral interactions between species at the interphase. The model equations were fitted to the measured data and model parameter values were determined by nonlinear regression analysis. The formation of bonds between ions and exchanger sites was evaluated by the equilibrium constant and the suppression of bond formation by electrostatic, geometric, and other lateral interactions was evaluated by the interaction constant. It was established that the properties of ions are determined by the valence, size, and hydration state of the ions. Monovalent ions (anions and cations) react with oxide surface hydroxyl and resin carboxyl sites as hydrated ions and form loose ion-site pairs by a weak electrostatic bond (nonspecific adsorption). However, the lateral interactions are large because of a large polarization of the ion-site pairs. When the

  8. Insoluble polyelectrolyte and ion-exchange hollow fiber impregnated therewith

    NASA Technical Reports Server (NTRS)

    Rembaum, A. (Inventor)

    1977-01-01

    The number of quaternary sites and ion exchange capacity of a polyquaternary, cross linked, insoluble copolymer of a vinyl pyridine and a dihalo organic compound is increased by about 15-35% by reaction of the polymer with an amine followed by quaternization, if required. The polymer forms spontaneously in the presence of a substrate such as within the pores of a hollow fiber. The improved resin impregnated fiber may be utilized to remove ions from waste or process steams.

  9. Specific ion effects on membrane potential and the permselectivity of ion exchange membranes.

    PubMed

    Geise, Geoffrey M; Cassady, Harrison J; Paul, Donald R; Logan, Bruce E; Hickner, Michael A

    2014-10-21

    Membrane potential and permselectivity are critical parameters for a variety of electrochemically-driven separation and energy technologies. An electric potential is developed when a membrane separates electrolyte solutions of different concentrations, and a permselective membrane allows specific species to be transported while restricting the passage of other species. Ion exchange membranes are commonly used in applications that require advanced ionic electrolytes and span technologies such as alkaline batteries to ammonium bicarbonate reverse electrodialysis, but membranes are often only characterized in sodium chloride solutions. Our goal in this work was to better understand membrane behaviour in aqueous ammonium bicarbonate, which is of interest for closed-loop energy generation processes. Here we characterized the permselectivity of four commercial ion exchange membranes in aqueous solutions of sodium chloride, ammonium chloride, sodium bicarbonate, and ammonium bicarbonate. This stepwise approach, using four different ions in aqueous solution, was used to better understand how these specific ions affect ion transport in ion exchange membranes. Characterization of cation and anion exchange membrane permselectivity, using these ions, is discussed from the perspective of the difference in the physical chemistry of the hydrated ions, along with an accompanying re-derivation and examination of the basic equations that describe membrane potential. In general, permselectivity was highest in sodium chloride and lowest in ammonium bicarbonate solutions, and the nature of both the counter- and co-ions appeared to influence measured permselectivity. The counter-ion type influences the binding affinity between counter-ions and polymer fixed charge groups, and higher binding affinity between fixed charge sites and counter-ions within the membrane decreases the effective membrane charge density. As a result permselectivity decreases. The charge density and polarizability

  10. Synthesis, Characterization and Ion Exchange of New Na/Nb/M(4+)/O/H(2)O(M=Ti,Zr) Phases

    SciTech Connect

    Nenoff, Tina M.; Nyman, May

    1999-05-07

    Due to the vast diversity of chemical media in which metal separations are executed, a wide range of ion separation materials are employed. This results in an ongoing effort to discover new phases with novel ion exchange properties. We present here the synthesis of a novel class of thermally and chemically stable microporous, niobate-based materials. Ion exchange studies show these new phases are highly selective for Sr2+ and other bivalent metals.

  11. Concentration profiles in heterogeneous ion-exchange membranes

    SciTech Connect

    Smirnova, N.M.; Glazkova, I.N.; Glukhova, L.P.; Murzinov, V.I.; Komarova, N.I.; Kvaratskheli, Yu.K.

    1982-05-10

    Concentration profiles of uranium and SO/sub 4//sup -2/ ions were determined in MKK-1 (based on KU-2 cation-exchange resin) and MAK-2 (based on AM anion-exchange resin) heterogeneous membranes in the course of diffusion and electrodialysis. The method employed for locating the position and determining the concentration of ions in a particular region of an ion-exchange material was local x-ray spectrochemical analysis with the aid of an electron probe. A solution containing 10g of U per liter and 0.5 N/sub 2/SO/sub 4/ was used as the ''transferring'' solution. Uranium is present in this solution in the form of UO/sub 2//sup 2 +/ cations and (UO/sub 2/(SO/sub 4/)/sub 2/)/sup 2 -/ and (UO/sub 2/(SO/sub 4/)/sub 3/)/sup 4 -/ anionic complexes, so that it is transported both through the cation-exchange and the anion-exchange membranes. The ''receiving'' solution was 0.1N H/sub 2/SO/sub 4/. The REMP-2 electron probe microanalyzer was used for recording the concentration profiles. The uranium L..cap alpha../sub 1/ line (lambda = 9.1 x 10/sup -11/m) and the sulfur K..cap alpha../sub 1,2/ line (lambda = 53.7 x 10/sup -11/m) were used as the analytical lines. The membrane conductivities, and the amount of uranium sorbed were determined at the same time. This investigation confirmed that the method of local x-ray spectrochemical analysis in conjunction with physicochemical investigations of the properties of ion-exchange membranes is a promising, reliable, and rapid method for studying the mechanism of ion transport in comparison with the use of multiplet devices. It can make mathematical modelling of transport processes considerably easier and more precise, as introduction of various assumptions is obviated.

  12. Charge Exchange with Highly Charged Ions

    NASA Astrophysics Data System (ADS)

    Glick, Jeremy; Ferri, Kevin; Schmitt, Jaclyn; Hanson, Joshua; Marler, Joan

    2016-05-01

    A detailed study of the physics of highly charged ions (HCIs) is critical for a deep understanding of observed phenomena resulting from interactions of HCIs with neutral atoms in astrophysical and fusion environments. Specifically the charge transfer rates and spectroscopy of the subsequent decay fluorescence are of great interest to these communities. Results from a laboratory based investigation of these rates will be presented. The experiment takes advantage of an energy and charge state selected beam of HCIs from the recently on-line Clemson University EBIT (CUEBIT). Progress towards an experimental apparatus for retrapping HCIs towards precision spectroscopy of HCIs will also be presented.

  13. Lanthanide ion (III) complexes of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraaminophosphonate for dual biosensing of pH with chemical exchange saturation transfer (CEST) and biosensor imaging of redundant deviation in shifts (BIRDS).

    PubMed

    Huang, Yuegao; Coman, Daniel; Ali, Meser M; Hyder, Fahmeed

    2015-01-01

    Relaxivity-based magnetic resonance of phosphonated ligands chelated with gadolinium (Gd(3+)) shows promise for pH imaging. However instead of monitoring the paramagnetic effect of lanthanide complexes on the relaxivity of water protons, biosensor (or molecular) imaging with magnetic resonance is also possible by detecting either the nonexchangeable or the exchangeable protons on the lanthanide complexes themselves. The nonexchangeable protons (e.g. -CHx, where 3 ≥ x ≥ 1) are detected using a three-dimensional chemical shift imaging method called biosensor imaging of redundant deviation in shifts (BIRDS), whereas the exchangeable protons (e.g. -OH or -NHy , where 2 ≥ y ≥ 1) are measured with chemical exchange saturation transfer (CEST) contrast. Here we tested the feasibility of BIRDS and CEST for pH imaging of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraaminophosphonate (DOTA-4AmP(8-)) chelated with thulium (Tm(3+) ) and ytterbium (Yb(3+)). BIRDS and CEST experiments show that both complexes are responsive to pH and temperature changes. Higher pH and temperature sensitivities are obtained with BIRDS for either complex when using the chemical shift difference between two proton resonances vs using the chemical shift of a single proton resonance, thereby eliminating the need to use water resonance as reference. While CEST contrast for both agents is linearly dependent on pH within a relatively large range (i.e. 6.3-7.9), much stronger CEST contrast is obtained with YbDOTA-4AmP(5-) than with TmDOTA-4AmP(5-). In addition, we demonstrate the prospect of using BIRDS to calibrate CEST as new platform for quantitative pH imaging.

  14. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ion-exchange resins. 173.25 Section 173.25 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Polymer Substances and Polymer...

  15. Determination of boron in silicates after ion exchange separation

    USGS Publications Warehouse

    Kramer, H.

    1955-01-01

    Existing methods for the determination of boron in silicates are not entirely satisfactory. Separation as the methyl ester is lengthy and frequently erratic. An accurate and rapid method applicable to glass, mineral, ore, and water samples uses ion exchange to remove interfering cations, and boron is determined titrimetrically in the presence of mannitol, using a pH meter to indicate the end point.

  16. Method and solvent composition for regenerating an ion exchange resin

    SciTech Connect

    Even, William R.; Irvin, David J.; Irvin, Jennifer A.; Tarver, Edward E.; Brown, Gilbert M.; Wang, James C. F.

    2002-01-01

    A method and composition for removing perchlorate from a highly selective ion exchange resin is disclosed. The disclosed approach comprises treating the resin in a solution of super critical or liquid carbon dioxide and one or more quaternary ammonium chloride surfactant compounds.

  17. EVALUATING ION EXCHANGE FOR REMOVING RADIUM FROM GROUNDWATER

    EPA Science Inventory

    This article, the second in a series, focuses on the results of bench- and pilot-scale studies of ion exchange processes for radium removal from groundwater in Lemont, Ill. Batch and column studies indicated a very high resin selectivity for radium compared with common cations. E...

  18. Copper Removal from A-01 Outfall by Ion Exchange

    SciTech Connect

    Oji, L.N.

    1999-02-17

    Chelex100, a commercially available ion exchange resin, has been identified in this study as having a significant affinity for copper and zinc in the A-01 outfall water. Removal of copper and zinc from A-01 outfall water will ensure that the outfall meets the state of South Carolina's limit on these heavy metals.

  19. Ion-exchanged glass waveguide amplifiers and lasers

    NASA Astrophysics Data System (ADS)

    Kevorkian, Antoine P.

    1998-04-01

    Planar devices made by ion-exchange provide efficient active or active/passive functions. Compact amplifiers with 24 dB single pass gain for a single 980 nm laser diode pumping are presented, as well as 1535 nm lasers with 27% slope efficiency.

  20. Cesium Ion Exchange Using Tank 241-AN-104 Supernate

    SciTech Connect

    Adu-Wusu, K.

    2003-12-22

    The River Protection Project is to design and build a high level nuclear waste treatment facility. The waste treatment plant is to process millions of gallons of radioactive waste stored in tanks at the Hanford Site. The high level nuclear waste treatment process includes various unit operations, such as ultrafiltration, precipitation, evaporation, ion exchange, and vitrification. Ion exchange is identified as the optimal treatment method for removal of cesium-137 and Tc-99 from the waste. Extensive ion exchange testing was performed using small-scale columns with actual waste samples. The objectives of this study were to: demonstrate SuperLig 644 ion exchange performance and process steps for the removal of cesium from actual AN-104 tank waste; pretreat actual AN-104 tank waste to reduce the concentration of cesium-137 in the waste below LAW vitrification limit; produce and characterize cesium eluate solutions for use in eluate evaporation tests. The experiments consisted of batch contact and small-scale column tests. The batch contact tests measured sorption partition coefficients Kds. The Kds were used to predict the effective resin capacity. The small-scale column tests, which closely mimic plant conditions, generated loading and elution profile data used to determine whether removal targets and design requirements were met.

  1. Thermal Analysis for Ion-Exchange Column System

    SciTech Connect

    Lee, Si Y.; King, William D.

    2012-12-20

    Models have been developed to simulate the thermal characteristics of crystalline silicotitanate ion exchange media fully loaded with radioactive cesium either in a column configuration or distributed within a waste storage tank. This work was conducted to support the design and operation of a waste treatment process focused on treating dissolved, high-sodium salt waste solutions for the removal of specific radionuclides. The ion exchange column will be installed inside a high level waste storage tank at the Savannah River Site. After cesium loading, the ion exchange media may be transferred to the waste tank floor for interim storage. Models were used to predict temperature profiles in these areas of the system where the cesium-loaded media is expected to lead to localized regions of elevated temperature due to radiolytic decay. Normal operating conditions and accident scenarios (including loss of solution flow, inadvertent drainage, and loss of active cooling) were evaluated for the ion exchange column using bounding conditions to establish the design safety basis. The modeling results demonstrate that the baseline design using one central and four outer cooling tubes provides a highly efficient cooling mechanism for reducing the maximum column temperature. In-tank modeling results revealed that an idealized hemispherical mound shape leads to the highest tank floor temperatures. In contrast, even large volumes of CST distributed in a flat layer with a cylindrical shape do not result in significant floor heating.

  2. Systematics of heavy-ion charge-exchange straggling

    NASA Astrophysics Data System (ADS)

    Sigmund, P.; Schinner, A.

    2016-10-01

    The dependence of heavy-ion charge-exchange straggling on the beam energy has been studied theoretically for several ion-target combinations. Our previous work addressed ions up to krypton, while the present study focuses on heavier ions, especially uranium. Particular attention has been paid to a multiple-peak structure which has been predicted theoretically in our previous work. For high-Z1 and high-Z2 systems, exemplified by U in Au, we identify three maxima in the energy dependence of charge-exchange straggling, while the overall magnitude is comparable with that of collisional straggling. Conversely, for U in C, charge-exchange straggling dominates, but only two peaks lie in the energy range where we presently are able to produce credible predictions. For U-Al we find good agreement with experiment in the energy range around the high-energy maximum. The position of the high-energy peak - which is related to processes in the projectile K shell - is found to scale as Z12 , in contrast to the semi-empirical Z13/2 dependence proposed by Yang et al. Measurements for heavy ions in heavy targets are suggested in order to reconcile a major discrepancy between the present calculations and the frequently-used formula by Yang et al.

  3. Ion-exchange behavior of alkali metals on treated carbons

    SciTech Connect

    Mohiuddin, G.; Hata, W.Y.; Tolan, J.S.

    1983-01-01

    The ion-exchange behavior of trace quantities of the alkali-metal ions sodium and cesium, on activated carbon impregnated with zirconium phosphate (referred to here as ZrP), was studied. Impregnated carbon had twice as much ion-exchange activity as unimpregnated, oxidized carbon, and 10 times as much as commercial activated carbons. The distribution coefficient of sodium increased with increasing pH; the distribution coefficient of cesium decreased with increasing pH. Sodium and cesium were separated with an electrolytic solution of 0.1 M HCl. Preliminary studies indicated that 0.2 M potassium and cesium can also be separated. Distribution coefficients of the supported ZrP were determined by the elution technique and agreed within 20% of the values for pure ZrP calculated from the literature.

  4. Separation of americium from curium by oxidation and ion exchange.

    PubMed

    Burns, Jonathan D; Shehee, Thomas C; Clearfield, Abraham; Hobbs, David T

    2012-08-21

    Nuclear energy has the potential to be a clean alternative to fossil fuels, but in order for it to play a major role in the US, many questions about the back end of the fuel cycle must be addressed. One of these questions is the difficult separation of americium from curium. Here, we report the oxidation of Am in two systems, perchloric acid and nitric acid and the affect of changing the acid has on the oxidation. K(d) values were observed and a direct separation factor was calculated and was seen to be as high as 20 for four metal(IV) pillared phosphate phosphonate inorganic organic hybrid ion exchange materials. These ion exchangers are characterized by very low selectivity for cations with low charge but extremely high uptake of ions of high charge.

  5. Graphene/Ionic Liquid Composite Films and Ion Exchange

    PubMed Central

    Mo, Yufei; Wan, Yunfang; Chau, Alicia; Huang, Fuchuan

    2014-01-01

    Wettability of graphene is adjusted by the formation of various ionic surfaces combining ionic liquid (IL) self-assembly with ion exchange. The functionalized ILs were designed and synthesized with the goal of obtaining adjustable wettability. The wettability of the graphene surface bearing various anions was measured systematically. The effect of solvent systems on ion exchange ratios on the graphene surface has also been investigated. Meanwhile, the mechanical properties of the graphene/IL composite films were investigated on a nanometer scale. The elasticity and adhesion behavior of the thin film was determined with respected to the indentation deformation by colloid probe nanoindentation method. The results indicate that anions played an important role in determining graphene/IL composite film properties. In addition, surface wetting and mechanics can be quantitatively determined according to the counter-anions on the surface. This study might suggest an alternate way for quantity detection of surface ions by surface force. PMID:24970602

  6. Oxygen-isotope exchange rates for three isostructural polyoxometalate ions.

    PubMed

    Villa, Eric M; Ohlin, C André; Casey, William H

    2010-04-14

    We compare oxygen-isotope exchange rates for all structural oxygens in three polyoxoniobate ions that differ by systematic metal substitutions of Ti(IV) --> Nb(V). The [H(x)Nb(10)O(28)]((6-x)-), [H(x)TiNb(9)O(28)]((7-x)-), and [H(x)Ti(2)Nb(8)O(28)]((8-x)-) ions are all isostructural yet have different Brønsted properties. Rates for sites within a particular molecule in the series differ by at least approximately 10(4), but the relative reactivities of the oxygen sites rank in nearly the same relative order for all ions in the series. Within a single ion, most structural oxygens exhibit rates of isotopic exchange that vary similarly with pH, indicating that each structure responds as a whole to changes in pH. Across the series of molecules, however, the pH dependencies for isotope exchanges and dissociation are distinctly different, reflecting different contributions from proton- or base-enhanced pathways. The proton-enhanced pathway for isotope exchange dominates at most pH conditions for the [H(x)Ti(2)Nb(8)O(28)]((8-x)-) ion, but the base-enhanced pathways are increasingly important for the [H(x)TiNb(9)O(28)]((7-x)-) and [H(x)Nb(10)O(28)]((6-x)-) structures at higher pH. The local effect of Ti(IV) substitution could be assessed by comparing rates for structurally similar oxygens on each side of the [H(x)TiNb(9)O(28)]((7-x)-) ion and is surprisingly small. Interestingly, these nanometer-size structures seem to manifest the same general averaged amphoteric chemistry that is familiar for other reactions affecting oxides in water, including interface dissolution by proton- and hydroxyl-enhanced pathways.

  7. Radon (222Rn) in ground water of fractured rocks: a diffusion/ion exchange model.

    PubMed

    Wood, Warren W; Kraemer, Thomas F; Shapiro, Allen

    2004-01-01

    Ground waters from fractured igneous and high-grade sialic metamorphic rocks frequently have elevated activity of dissolved radon (222Rn). A chemically based model is proposed whereby radium (226Ra) from the decay of uranium (238U) diffuses through the primary porosity of the rock to the water-transmitting fracture where it is sorbed on weathering products. Sorption of 226Ra on the fracture surface maintains an activity gradient in the rock matrix, ensuring a continuous supply of 226Ra to fracture surfaces. As a result of the relatively long half-life of 226Ra (1601 years), significant activity can accumulate on fracture surfaces. The proximity of this sorbed 226Ra to the active ground water flow system allows its decay progeny 222Rn to enter directly into the water. Laboratory analyses of primary porosity and diffusion coefficients of the rock matrix, radon emanation, and ion exchange at fracture surfaces are consistent with the requirements of a diffusion/ion-exchange model. A dipole-brine injection/withdrawal experiment conducted between bedrock boreholes in the high-grade metamorphic and granite rocks at the Hubbard Brook Experimental Forest, Grafton County, New Hampshire, United States (42 degrees 56'N, 71 degrees 43'W) shows a large activity of 226Ra exchanged from fracture surfaces by a magnesium brine. The 226Ra activity removed by the exchange process is 34 times greater than that of 238U activity. These observations are consistent with the diffusion/ion-exchange model. Elutriate isotopic ratios of 223Ra/226Ra and 238U/226Ra are also consistent with the proposed chemically based diffusion/ion-exchange model.

  8. Radon (222Rn) in ground water of fractured rocks: A diffusion/ion exchange model

    USGS Publications Warehouse

    Wood, W.W.; Kraemer, T.F.; Shapiro, A.

    2004-01-01

    Ground waters from fractured igneous and high-grade sialic metamorphic rocks frequently have elevated activity of dissolved radon (222Rn). A chemically based model is proposed whereby radium (226Ra) from the decay of uranium (238U) diffuses through the primary porosity of the rock to the water-transmitting fracture where it is sorbed on weathering products. Sorption of 226Ra on the fracture surface maintains an activity gradient in the rock matrix, ensuring a continuous supply of 226Ra to fracture surfaces. As a result of the relatively long half-life of 226Ra (1601 years), significant activity can accumulate on fracture surfaces. The proximity of this sorbed 226Ra to the active ground water flow system allows its decay progeny 222Rn to enter directly into the water. Laboratory analyses of primary porosity and diffusion coefficients of the rock matrix, radon emanation, and ion exchange at fracture surfaces are consistent with the requirements of a diffusion/ion- exchange model. A dipole-brine injection/withdrawal experiment conducted between bedrock boreholes in the high-grade metamorphic and granite rocks at the Hubbard Brook Experimental Forest, Grafton County, New Hampshire, United States (42??56???N, 71??43???W) shows a large activity of 226Ra exchanged from fracture surfaces by a magnesium brine. The 226Ra activity removed by the exchange process is 34 times greater than that of 238U activity. These observations are consistent with the diffusion/ion-exchange model. Elutriate isotopic ratios of 223Ra/226Ra and 238U/226Ra are also consistent with the proposed chemically based diffusion/ion-exchange model.

  9. Environmentally benign hardness removal using ion-exchange fibers and snowmelt.

    PubMed

    Greenleaf, John E; Sengupta, Arup K

    2006-01-01

    Many industrial unit operations and unit processes require near-complete removal of hardness to avoid scaling in heat-transfer equipment, fouling in membranes, and high consumption of detergents and sequestering chemicals in cooling and wash water. Lime softening and cation exchange are the most commonly used processes practiced to date for hardness removal. Herein, we report and discuss the results and attributes of a new hardness removal process using ion-exchange fibers (IX-fibers). Most importantly, the process uses harvested snowmelt (or rainwater) as the regenerant chemical along with sparged carbon dioxide. Consequently, the spent regenerant does not contain a high concentration of aggressive chemicals such as sodium chloride or acid like traditional ion-exchange processes nor does the process produce voluminous sludges similar to lime softening. The bulk of carbon dioxide consumed during regeneration remains sequestered in the aqueous phase as alkalinity. IX-fibers form the heart of the process. They are essentially thin cylindrical polymeric strands 10-20 microm in diameter. The weak-acid carboxylate functional groups reside near to the surface of these cylindrical fibers. Low intraparticle diffusional resistance is the underlying reason IX-fibers are amenable to efficient regeneration with snowmelt sparged with carbon dioxide. When the carbon dioxide partial pressure is increased to 6.8 atm, over 90% calcium desorption efficiency is obtained. On the contrary, commercial weak-acid ion-exchange resins in spherical bead forms are ineffective for regeneration with carbon-dioxide-sparged snowmelt due to extremely slow ion-exchange kinetics involving counter-transport of Ca2+ and H+.

  10. Using ion exchange chromatography to purify a recombinantly expressed protein.

    PubMed

    Duong-Ly, Krisna C; Gabelli, Sandra B

    2014-01-01

    Ion exchange chromatography (IEX) separates molecules by their surface charge, a property that can vary vastly between different proteins. There are two types of IEX, cation exhange and anion exchange chromatography. The protocol that follows was designed by the authors for anion exchange chromatography of a recombinantly expressed protein having a pI of 4.9 and containing two cysteine residues and one tryptophan residue, using an FPLC system. Prior to anion exchange, the protein had been salted out using ammonium sulfate precipitation and partially purified via hydrophobic interaction chromatography (see Salting out of proteins using ammonium sulfate precipitation and Use and Application of Hydrophobic Interaction Chromatography for Protein Purification). Slight modifications to this protocol may be made to accommodate both the protein of interest and the availability of equipment.

  11. Highly sensitive determination of hydrazine ion by ion-exclusion chromatography with ion-exchange enhancement of conductivity detection.

    PubMed

    Mori, Masanobu; Tanaka, Kazuhiko; Xu, Qun; Ikedo, Mikaru; Taoda, Hiroshi; Hu, Wenzhi

    2004-06-11

    An ion-exclusion chromatography method with ion-exchange enhancement of conductivity was developed for the selective separation and sensitive determination of hydrazine ion from alkali/alkaline earth metal cations and ammonium ion. Hydrazine ion was separated by ion-exclusion/penetration effect from other cations on a weakly basic anion-exchange column in the OH- form (TSKgel DEAE-5PW). Moreover, two different ion-exchange resin columns were inserted between the separating column and conductimetric detector in order to improve the sensitivity of hydrazine ion. The first enhancement column packed with a strongly basic anion-exchange resin in the SO4(2-) form (TSKgel SAX) for hydrazine ion can convert from N2H5OH to (N2H5)2SO4. Moreover, the second enhancement column packed with a strongly acidic cation-change resin in the H+ form (TSKgel SCX) can convert to H2SO4. As a result, the sensitivity of hydrazine ion using two conductivity enhancement columns could be 26.8-times greater than using the separating column alone. This method was effectiveness also for the enhancement of ammonium ion (6.1-times) and sodium ion (1.2-times). The calibration graph of hydrazine ion detected as H2SO4 was linear over the concentration range of 0.001-100 ppm (r2 = 0.9988). The detection limit of hydrazine ion in this system was 0.64 ppb. Therefore, hydrazine ion in real boiler water sample could be accurately determined, avoiding the interference of other cations.

  12. Studies on the solid-state ion exchange of nickel ions into zeolites using DRS technique

    NASA Astrophysics Data System (ADS)

    Zanjanchi, M. A.; Ebrahimian, A.

    2004-05-01

    The coordination of Ni 2+ ions in the dehydrated nickel-exchanged zeolites was investigated from the analysis of diffuse reflectance spectra. Solid-state ion exchange method was used to prepare nickel-containing mordenite, Y, L and mazzite zeolites. In the dehydrated mordenite and zeolite Y, nickel cations are presented in both forms of tetrahedral and distorted tetrahedral symmetries. The relative amount of tetrahedral and distorted tetrahedral nickel species are related to the heating temperature and heating time used for calcinations. In the dehydrated zeolite L and mazzite, Ni 2+ ions are mainly in the distorted octahedral symmetries.

  13. Preparation and characterization of 5-sulphosalicylic acid doped tetraethoxysilane composite ion-exchange material by sol-gel method.

    PubMed

    Rehman, Suhail-ul; Islam, Nasarul; Ahad, Sozia; Fatima, Syed Zeeshan; Pandith, Altaf Hussain

    2013-09-15

    In this manuscript, we report the preparation and characterization of sulphosalicylic doped tetraethoxysilane (SATEOS), composite material by sol-gel method as a new ion exchanger for the removal of Ni(II) from aqueous solution. The fine granular material was prepared by acid catalyzed condensation polymerization through sol-gel mechanism in the presence of cationic surfactant. The material has an ion exchange capacity of 0.64 mequiv./g(dry) for sodium ions, 0.60 mequiv./g(dry) for potassium ions, 1.84 mequiv./g(dry) for magnesium ions, 1.08 mequiv./g(dry) for calcium ions and 1.36 mequiv./g(dry) for strontium ions. Its X-ray diffraction studies suggest that it is crystalline in nature. The material has been characterized by SEM, IR, TGA and DTG so as to identify the various functional groups and ion exchange sites present in this material. Quantum chemical computations at DFT/B3LYP/6-311G (d,p) level on model systems were performed to substantiate the structural conclusions based ion instrumental techniques. Investigations into the elution behaviour, ion exchange reversibility and distribution capacities of this material towards certain environmentally hazardous metal ions are also performed. The material shows good chemical stability towards acidic conditions and exhibits fast elution of exchangeable H(+) ions under neutral conditions. This material shows remarkable selectivity for Ni(II) and on the basis of its Kd value (4×10(2) in 0.01M HClO4) some binary separations of Ni(II) from other metal ions are performed.

  14. Fluorescent nanosensors for intracellular chemical analysis: decyl methacrylate liquid polymer matrix and ion-exchange-based potassium PEBBLE sensors with real-time application to viable rat C6 glioma cells.

    PubMed

    Brasuel, M; Kopelman, R; Miller, T J; Tjalkens, R; Philbert, M A

    2001-05-15

    Fluorescent spherical nanosensors, or PEBBLEs (probes encapsulated by biologically localized embedding), in the 500 nm-1 microm size range have been developed using decyl methacrylate as a matrix. A general scheme for the polymerization and introduction of sensing components creates a matrix that allows for the utilization of the highly selective ionophores used in poly(vinyl chloride) and decyl methacrylate ion-selective electrodes. We have applied these optically silent ionophores to fluorescence-based sensing by using ion-exchange and highly selective pH chromoionophores. This allows the tailoring of selective submicrometer sensors for use in intracellular measurements of important analytes for which selective enough fluorescent probes do not exist. The protocol for sensor development has been worked out for potassium sensing. It is based on the BME-44 ionophore (2-dodecyl-2-methyl-1,3-propanediylbis[N-[5'nitro(benzo-15-crown-5)-4'-yl]carbamate]). The general scheme should work for any available ionophore used in PVC or decyl methacrylate ion-selective electrodes, with minor adjustments to account for differences in ionophore charge and analyte binding constant. The reversible and highly selective sensors developed have a subsecond response time and an adjustable dynamic range. Applications to live C6 glioma cells demonstrate their utility; the intracellular potassium activity is followed in real time upon extracellular administration of kainic acid.

  15. Adsorption of fluoride, phosphate, and arsenate ions on a new type of ion exchange fiber.

    PubMed

    Ruixia, Liu; Jinlong, Guo; Hongxiao, Tang

    2002-04-15

    A new type of ion exchange fiber for the removal of fluoride, phosphate, and arsenate ions has been developed. A batch adsorption technique for investigating adsorption kinetic and equilibrium parameters and determining pH adsorption edges is applied. It is shown that the adsorption properties of the ion exchange fiber for fluoride, phosphate, and arsenate ions depend on the pH value and anion concentration. The adsorption of arsenate on the sorbent reaches a maximum of 97.9% in the pH value range of 3.5 to 7.0. The adsorption percentage of phosphate is more than 99% in the pH range of 3.0 to 5.5. The adsorption of fluoride on the ion exchange fiber is found to be 90.4% at pH 3.0. The Freundlich model can describe the adsorption equilibrium data of fluoride, arsenate, and phosphate anions. The sorption of the three anions on the ion exchange fiber is a rapid process, and the adsorption kinetic data can be simulated very well by the pseudo-second-order rate equation. The column performance is carried out to assess the applicability of the ion exchange fiber for the removal of fluoride, phosphate, and arsenate ions from synthetic wastewaters with satisfactory removal efficiency. The desorption experiment shows that fluoride ion sorbed by the fiber column can be quantitatively desorbed with 5 mL of 0.50 mol/L NaOH at elution rate of 1 mL/min, and 30 mL of NaOH is necessary for the quantitative recovery of phosphate and arsenate ions.

  16. Ion exchange selectivity for cross-linked polyacrylic acid

    NASA Technical Reports Server (NTRS)

    May, C. E.; Philipp, W. H.

    1983-01-01

    The ion separation factors for 21 common metal ions with cross-linked polyacrylic acid were determined as a function of pH and the percent of the cross-linked polyacrylic acid neutralized. The calcium ion was used as a reference. At a pH of 5 the decreasing order of affinity of the ions for the cross-linked polyacrylic acid was found to be: Hg++, Fe+++, Pb++, Cr+++, Cu++, Cd++, Al+++, Ag+, Zn++, Ni++, Mn++, Co++, Ca++, Sr++, Ba++, Mg++, K+, Rb+, Cs+, Na+, and Li+. Members of a chemical family exhibited similar selectivities. The Hg++ ion appeared to be about a million times more strongly bound than the alkali metal ions. The relative binding of most of the metal ions varied with pH; the very tightly and very weakly bound ions showed the largest variations with pH. The calcium ion-hydrogen ion equilibrium was perturbed very little by the presence of the other ions. The separation factors and selectivity coefficients are discussed in terms of equilibrium and thermodynamic significance.

  17. Synthesis and Characterization of Perfluoro Quaternary Ammonium Ion Exchange Membranes for Fuel Cell Applications

    DTIC Science & Technology

    2012-01-01

    TERMS Perfluoroinated polymer; anion exchange membrane; morphology; base stability Mellisa A. Vandiver, Soenke Seifert, Matthew W. Liberatore, Andrew...humidities. Better understanding of the role of water and polymer morphology on the ion conduction and stability of AEMs is necessary for practical AEM fuel...sufficient chemical and mechanical stability (5, 10) For these reasons PFSAs remain the benchmark comparison for all new PEMs and AEMs (1, 11). The

  18. Mechanism of extracellular ion exchange and binding-site occlusion in a sodium/calcium exchanger

    SciTech Connect

    Liao, Jun; Marinelli, Fabrizio; Lee, Changkeun; Huang, Yihe; Faraldo-Gomez, Jose D.; Jiang, Youxing

    2016-05-16

    Na+/Ca2+ exchangers utilize the Na+ electrochemical gradient across the plasma membrane to extrude intracellular Ca2+, and play a central role in Ca2+ homeostasis. Here, we elucidate their mechanisms of extracellular ion recognition and exchange through a structural analysis of the exchanger from Methanococcus jannaschii (NCX_Mj) bound to Na+, Ca2+ or Sr2+ in various occupancies and in an apo state. This analysis defines the binding mode and relative affinity of these ions, establishes the structural basis for the anticipated 3:1Na+/Ca2+ exchange stoichiometry, and reveals the conformational changes at the onset of the alternating-access transport mechanism. An independent analysis of the dynamics and conformational free-energy landscape of NCX_Mj in different ion-occupancy states, based on enhanced-sampling molecular-dynamics simulations, demonstrates that the crystal structures reflect mechanistically relevant, interconverting conformations. Lastly, these calculations also reveal the mechanism by which the outward-to-inward transition is controlled by the ion-occupancy state, thereby explaining the emergence of strictly-coupled Na+/Ca2+ antiport.

  19. Mechanism of extracellular ion exchange and binding-site occlusion in the sodium-calcium exchanger

    PubMed Central

    Lee, ChangKeun; Huang, Yihe; Faraldo-Gómez, José D.; Jiang, Youxing

    2016-01-01

    Na+/Ca2+ exchangers utilize the Na+ electrochemical gradient across the plasma membrane to extrude intracellular Ca2+, and play a central role in Ca2+ homeostasis. Here, we elucidate their mechanisms of extracellular ion recognition and exchange through a structural analysis of the exchanger from Methanococcus jannaschii (NCX_Mj) bound to Na+, Ca2+ or Sr2+ in various occupancies and in an apo state. This analysis defines the binding mode and relative affinity of these ions, establishes the structural basis for the anticipated 3Na+:1Ca2+ exchange stoichiometry, and reveals the conformational changes at the onset of the alternating-access transport mechanism. An independent analysis of the dynamics and conformational free-energy landscape of NCX_Mj in different ion-occupancy states, based on enhanced-sampling molecular-dynamics simulations, demonstrates that the crystal structures reflect mechanistically relevant, interconverting conformations. These calculations also reveal the mechanism by which the outward-to-inward transition is controlled by the ion-occupancy state, thereby explaining the emergence of strictly-coupled Na+/Ca2+ antiport. PMID:27183196

  20. Mechanism of extracellular ion exchange and binding-site occlusion in a sodium/calcium exchanger

    DOE PAGES

    Liao, Jun; Marinelli, Fabrizio; Lee, Changkeun; ...

    2016-05-16

    Na+/Ca2+ exchangers utilize the Na+ electrochemical gradient across the plasma membrane to extrude intracellular Ca2+, and play a central role in Ca2+ homeostasis. Here, we elucidate their mechanisms of extracellular ion recognition and exchange through a structural analysis of the exchanger from Methanococcus jannaschii (NCX_Mj) bound to Na+, Ca2+ or Sr2+ in various occupancies and in an apo state. This analysis defines the binding mode and relative affinity of these ions, establishes the structural basis for the anticipated 3:1Na+/Ca2+ exchange stoichiometry, and reveals the conformational changes at the onset of the alternating-access transport mechanism. An independent analysis of the dynamicsmore » and conformational free-energy landscape of NCX_Mj in different ion-occupancy states, based on enhanced-sampling molecular-dynamics simulations, demonstrates that the crystal structures reflect mechanistically relevant, interconverting conformations. Lastly, these calculations also reveal the mechanism by which the outward-to-inward transition is controlled by the ion-occupancy state, thereby explaining the emergence of strictly-coupled Na+/Ca2+ antiport.« less

  1. Field performance of GCL under ion exchange conditions

    SciTech Connect

    James, A.N.; Fullerton, D.; Drake, R.

    1997-10-01

    Five Victorian reservoirs of brick pillar and arch construction were renovated using geosynthetic clay liners (also called bentonite/geosynthetic composites) (GCL) as roof sealing materials. The GCL was predominantly sodium bentonite and contained some 2% of calcite. GCLs were laid on leveled, original puddled clay packed between and above the brick arches. There was an overlying gravel layer connected to a drainage system that, in turn, was covered with soil and seeded with grass. Leaks through roofs into stored potable water were discovered. Excavation and exposure of the GCL showed that they were finely cracked in many places. Samples of the GCL bentonite from several locations at each of five sites had a high moisture content. Also, the GCL had a much reduced exchangeable sodium and increased exchangeable calcium content when compared to the dry unused GCL. Laboratory experiments, lasting for a limited period, were carried out to simulate operating conditions of the GCL whereby water falling on the ground and reaching the GCL flowed across the GCL in the overlying gravel layer to collector drains. Similar but less extensive ion exchange, calcium for sodium, was found here also. The evidence demonstrates that calcium from calcite, contained in the GCL bentonite, exchanged with sodium and, in so doing, contributed to shrinkage and cracking. Supplementary sources of calcium for ion exchange probably came from overlying calcareous soil and water from firehoses used to field test the integrity of the GCL.

  2. Charge-exchange plasma generated by an ion thruster

    NASA Technical Reports Server (NTRS)

    Kaufman, H. R.

    1975-01-01

    The use of high voltage solar arrays greatly reduces or eliminates power processing requirements in space electric propulsion systems. This use also requires substantial areas of solar array to be at high positive potential relative to space and most of the spacecraft. The charge exchange plasma conducts electrons from the ion beam to such positive surfaces, and thereby electrically load the high voltage solar array. To evaluate this problem, the charge-exchange plasma generated by an ion beam was investigated experimentally. Based upon the experimental data, a simple model was derived for the charge-exchange plasma. This model is conservative in the sense that both the electron/ion density and the electron current density should be equal to, or less than, the preducted value for all directions in the hemisphere upstream of the ion beam direction. Increasing the distance between a positive potential surface (such as a high voltage solar array) and the thruster is the simplest way to control interactions. Both densities and currents vary as the inverse square of this distance.

  3. Demonstration of an Ion Exchange Resin Addition/Removal System with Superlig 659

    SciTech Connect

    Norato, M.A.

    2000-12-19

    A pilot facility was designed and built in the Thermal Fluids Laboratory at the Savannah River Technology Center to demonstrate the slurry transport of ion exchange resins in and out of ion exchange columns.

  4. Synthesis, structural characterization, and performance evaluation of resorcinol-formaldehyde (R-F) ion-exchange resin

    SciTech Connect

    Hubler, T.L.; Franz, J.A.; Shaw, W.J.; Bryan, S.A.; Hallen, R.T.; Brown, G.N.; Bray, L.A.; Linehan, J.C.

    1995-08-01

    The 177 underground storage tanks at the DOE`s Hanford Site contain an estimated 180 million tons of high-level radioactive wastes. It is desirable to remove and concentrate the highly radioactive fraction of the tank wastes for vitrification. Resorcinol-formaldehyde (R-F) resin, an organic ion-exchange resin with high selectivity and capacity for the cesium ion, which is a candidate ion-exchange material for use in remediation of tank wastes. The report includes information on the structure/function analysis of R-F resin and the synthetic factors that affect performance of the resin. CS-100, a commercially available phenol-formaldehyde (P-F) resin, and currently the baseline ion-exchanger for removal of cesium ion at Hanford, is compared with the R-F resin. The primary structural unit of the R-F resin was determined to consist of a 1,2,3,4-tetrasubstituted resorcinol ring unit while CS-100, was composed mainly of a 1,2,4-trisubstituted ring. CS-100 shows the presence of phenoxy-ether groups, and this may account for the much lower decontamination factor of CS-100 for cesium ion. Curing temperatures for the R-F resin were found to be optimal at 105--130C. At lower temperatures, insufficient curing, hence crosslinking, of the polymer resin occurs and selectivity for cesium drops. Curing at elevated temperatures leads to chemical degradation. Optimal particle size for R-F resin is in the range of 20--50 mesh-sized particles. R-F resin undergoes chemical degradation or oxidation which destroys ion-exchange sites. The ion-exchange sites (hydroxyl groups) are converted to quinones and ketones. CS-100, though it has much lower performance for cesium ion-exchange, is significantly more chemically stable than R-F resin. To gamma radiation, CS-100 is more radiolytically stable than R-F resin.

  5. Membrane consisting of polyquaternary amine ion exchange polymer network interpenetrating the chains of thermoplastic matrix polymer

    NASA Technical Reports Server (NTRS)

    Rembaum, A.; Wallace, C. J. (Inventor)

    1978-01-01

    An ion exchange membrane was formed from a solution containing dissolved matrix polymer and a set of monomers which are capable of reacting to form a polyquaternary ion exchange material; for example vinyl pyride and a dihalo hydrocarbon. After casting solution and evaporation of the volatile component's, a relatively strong ion exchange membrane was obtained which is capable of removing anions, such as nitrate or chromate from water. The ion exchange polymer forms an interpenetrating network with the chains of the matrix polymer.

  6. Enigmatic ion-exchange behavior of myo-inositol phosphates.

    PubMed

    Shelor, C Phillip; Liao, Hongzhu; Kadjo, Akinde Florence; Dasgupta, Purnendu K

    2015-05-05

    The separation of myo-inositol mono-, di-, tri-, tetra-, pentakis-, and hexakisphosphate (InsP1, InsP2, InsP3, InsP4, InsP5, InsP6) was carried out using hydroxide eluent ion chromatography. Acid hydrolysis of InsP6 (phytate) was used to prepare a distribution of InsPs, ranging from InsP1 to InsP5's and including unhydrolyzed InsP6. Counting all possible positional isomers (many of which have stereoisomers that will not be separable by conventional ion exchange), 40 chromatographically separable peaks are possible; up to 22 were separated and identified by mass spectrometry. InsPs show unusual ion-exchange behavior in two respects: (a) the retention order is not monotonically related with the charge on the ion and (b) at the same hydroxide eluent concentration, retention is greatly dependent on the eluent metal cation. The retention of InsP3-InsP6 was determined to be controlled by steric factors while elution was influenced by eluent cation complexation. These highly phosphorylated InsPs have a much greater affinity for alkali metals (Li(+) > Na(+) > K(+)) than quaternary ammonium ions. This difference in cation affinity was exploited to improve separation through the use of a tetramethylammonium hydroxide-sodium hydroxide gradient.

  7. Ion exchange at the critical point of solution.

    PubMed

    Savoy, J D; Baird, J K; Lang, J R

    2016-03-11

    A mixture of isobutyric acid (IBA)+water has an upper critical point of solution at 26.7°C and an IBA concentration of 4.40M. We have determined the Langmuir isotherms for the hydroxide form of Amberlite IRN-78 resin in contact with mixtures of IBA+water at temperatures, 27.0, 29.0, 31.0 and 38.0°C, respectively. The Langmuir plot at 38.0°C forms a straight line. At the three lower temperatures, however, a peak in the Langmuir plot is observed for IBA concentrations in the vicinity of 4.40M. We regard this peak to be a critical effect not only because it is located close to 4.40M, but also because its height becomes more pronounced as the temperature of the isotherm approaches the critical temperature. For concentrations in the vicinity of the peak, the data indicate that the larger isobutyrate ion is rejected by the resin in favor of the smaller hydroxide ion. This reversal of the expected ion exchange reaction might be used to separate ions according to size. Using the Donnan theory of ion exchange equilibrium, we link the swelling pressure to the osmotic pressure. We show that the peak in the Langmuir plot is associated with a maximum in the "osmotic" energy. This maximum has its origin in the concentration derivative of the osmotic pressure, which goes to zero as the critical point is approached.

  8. Chemical tools for detecting Fe ions

    PubMed Central

    Hirayama, Tasuku; Nagasawa, Hideko

    2017-01-01

    Owing to its distinctive electrochemical properties with interconvertible multiple oxidation states, iron plays a significant role in various physiologically important functions such as respiration, oxygen transport, energy production, and enzymatic reactions. This redox activity can also potentially produce cellular damage and death, and numerous diseases are related to iron overload resulting from the dysfunction of the iron regulatory system. In this case, “free iron” or “labile iron,” which refers to iron ion weakly bound or not bound to proteins, causes aberrant production of reactive oxygen species. With the aim of elucidating the variation of labile iron involved in pathological processes, some chemical tools that can qualitatively and/or quantitatively monitor iron have been utilized to investigate the distribution, accumulation, and flux of biological iron species. Since iron ions show unique reactivity depending on its redox state, i.e., Fe2+ or Fe3+ (or transiently higher oxidative states), methods for the separate detection of iron species with different redox states are preferred to understand its physiological and pathological roles more in detail. The scope of this review article covers from classical chromogenic to newly emerging chemical tools for the detection of Fe ions. In particular, chemical tools applicable to biological studies will be presented. PMID:28163381

  9. Isotope effects of neodymium in different ligands exchange systems studied by ion exchange displacement chromatography.

    PubMed

    Ismail, Ibrahim; Fawzy, Ahmed S; Ahmad, Mohammad I; Aly, Hisham F; Nomura, Masao; Fujii, Yasuhiko

    2013-03-01

    The isotope effects of neodymium in Nd-glycolate ligand exchange system were studied by using ion exchange chromatography. The separation coefficients of neodymium isotopes, ε's, were calculated from the observed isotopic ratios at the front and rear boundaries of the neodymium adsorption band. The values of separation coefficients of neodymium isotopes, ε's, for the Nd-glycolate ligand exchange system were compared with those of Nd-malate and Nd-citrate, which indicated that the isotope effects of neodymium as studied by the three ligands takes the following direction Malate > Citrate > Glycolate. This order agrees with the number of available sites for complexation of each ligand. The values of the plate height, HETP of Nd in Nd-ligand exchange systems were also calculated.

  10. Isotope effects of neodymium in different ligands exchange systems studied by ion exchange displacement chromatography

    PubMed Central

    Ismail, Ibrahim; Fawzy, Ahmed S.; Ahmad, Mohammad I.; Aly, Hisham F.; Nomura, Masao; Fujii, Yasuhiko

    2012-01-01

    The isotope effects of neodymium in Nd-glycolate ligand exchange system were studied by using ion exchange chromatography. The separation coefficients of neodymium isotopes, ε’s, were calculated from the observed isotopic ratios at the front and rear boundaries of the neodymium adsorption band. The values of separation coefficients of neodymium isotopes, ε’s, for the Nd-glycolate ligand exchange system were compared with those of Nd-malate and Nd-citrate, which indicated that the isotope effects of neodymium as studied by the three ligands takes the following direction Malate > Citrate > Glycolate. This order agrees with the number of available sites for complexation of each ligand. The values of the plate height, HETP of Nd in Nd-ligand exchange systems were also calculated. PMID:25685410

  11. RECENT ADVANCES IN ION EXCHANGE MATERIALS AND PROCESSES FOR POLLUTION PREVENTION

    EPA Science Inventory

    The goal of this article was to summarize the recent advances in ion exchange technology for the metal finishing industry. Even though the ion exchange technology is mature and is widely employed in the industry, new applications, approaches and ion exchange materials are emergi...

  12. ION EXCHANGE PROCESS FOR THE RECOVERY AND PURIFICATION OF MATERIALS

    DOEpatents

    Long, R.S.; Bailes, R.H.

    1958-04-15

    A process for the recovery of certain metallic ions from aqueous solutions by ion exchange techniques is described. It is applicable to elements such as vanadium, chromium, nnanganese, and the like, which are capable of forming lower valent cations soluble in aqueous solutions and which also form ldgher valent anions soluble in aqueous acidic solutions. For example, small amounts of vanadium occurring in phosphoric acid prepared from phosphate rock may be recovered by reducing the vanadium to a trivalent cation adsorbing; the vanadium in a cationic exchange resin, then treating the resin with a suitable oxidizing agent to convert the adsorbed vanadium to a higher valent state, and finally eluting; the vanadium as an anion from the resin by means of an aqueous acidic solution.

  13. Hybrid metallic ion-exchanged waveguides for SPR biological sensing

    NASA Astrophysics Data System (ADS)

    de Bonnault, S.; Bucci, D.; Zermatten, P.. J.; Charette, P. G.; Broquin, J. E.

    2015-02-01

    Glass substrates have been used for decades to create biosensors due to their biocompatibility, low thermal conductivity, and limited fluorescence. Among the different types of sensors, those based on surface plasmon resonance (SPR) allow exploitation of the sensing lightwave at the vicinity of the sensor surface where small entities such as DNA or proteins are located. In this paper, ion-exchanged waveguides and SPR are combined to create a multianalyte optical sensor integrated onto glass. First the principle of operation is introduced, then the theoretical analysis and design of the sensing element. Simulations have been carried out using the Aperiodic Fourier Modal Method (AFMM) and a custom software that handles ion-exchange index-profiles. Fabrication and characterization processes are also presented. Finally the first experimental spectra are displayed and discussed. The sensor presents a bulk sensibility of 5000nm/RIU.

  14. Why relevant chemical information cannot be exchanged without disclosing structures

    NASA Astrophysics Data System (ADS)

    Filimonov, Dmitry; Poroikov, Vladimir

    2005-09-01

    Both society and industry are interested in increasing the safety of pharmaceuticals. Potentially dangerous compounds could be filtered out at early stages of R&D by computer prediction of biological activity and ADMET characteristics. Accuracy of such predictions strongly depends on the quality & quantity of information contained in a training set. Suggestion that some relevant chemical information can be added to such training sets without disclosing chemical structures was generated at the recent ACS Symposium. We presented arguments that such safety exchange of relevant chemical information is impossible. Any relevant information about chemical structures can be used for search of either a particular compound itself or its close analogues. Risk of identifying such structures is enough to prevent pharma industry from relevant chemical information exchange.

  15. Ion exchange and adsorption on low rank coals for liquefaction

    SciTech Connect

    Vorres, K.S.

    1995-08-01

    The objectives of this program involve the study of the catalysis of liquefaction of low rank coals. Ion exchange and adsorption techniques are being used or modified to incorporate catalytically active metals into coal samples. Relative oil yields will be determined by Sandia National Laboratory and PETC collaborators to establish the effectiveness of the catalyst incorporation techniques. This report describes work done over the past 12 months of an on-going project.

  16. Integrated optic broadband duplexer made by ion exchange

    NASA Astrophysics Data System (ADS)

    Ghibaudo, E.; Broquin, J.-E.; Benech, P.

    2003-02-01

    The development of optical amplification and bidirectional traffic in local and wide area networks requires broadband multiplexers which are able to treat the signal of an entire telecommunication window. A device made by ion exchange and answering to these needs is proposed in this letter. Its working principle, based on a leaky structure is first explained. An experimental result confirming a good broadband spectral behavior is then presented. Its spectral response displays two duplexing bands of at least 100 nm.

  17. Separation of organic ion exchange resins from sludge -- engineering study

    SciTech Connect

    Duncan, J.B.

    1998-08-25

    This engineering study evaluates the use of physical separation technologies to separate organic ion exchange resin from KE Basin sludge prior to nitric acid dissolution. This separation is necessitate to prevent nitration of the organics in the acid dissolver. The technologies under consideration are: screening, sedimentation, elutriation. The recommended approach is to first screen the Sludge and resin 300 microns then subject the 300 microns plus material to elutriation.

  18. Electrodeposition of microparticles on polarized ion exchange membranes

    SciTech Connect

    Verbich, S.V.; Ponomarev, M.I.; Grebenyuk, V.D.; Dukhin, S.S.

    1986-11-01

    The use of ion exchange membranes to extract microparticles from an aqueous solution is considered. The efficiency of removing negatively charged aerosil particles depends substantially on the nature of the membrane located at the anode. It has been established that besides an increase in the electric field intensity the principal factor ensuring an increase in the efficiency of purifying a solution by electrodeposition of microparticles on a membrane surface is a reduction in the flowrate relative to the membrane surface.

  19. Momentum transfer in relativistic heavy ion charge-exchange reactions

    NASA Technical Reports Server (NTRS)

    Townsend, L. W.; Wilson, J. W.; Khan, F.; Khandelwal, G. S.

    1991-01-01

    Relativistic heavy ion charge-exchange reactions yield fragments (Delta-Z = + 1) whose longitudinal momentum distributions are downshifted by larger values than those associated with the remaining fragments (Delta-Z = 1, -2,...). Kinematics alone cannot account for the observed downshifts; therefore, an additional contribution from collision dynamics must be included. In this work, an optical model description of collision momentum transfer is used to estimate the additional dynamical momentum downshift. Good agreement between theoretical estimates and experimental data is obtained.

  20. Investigation of chemical exchange at intermediate exchange rates using a combination of chemical exchange saturation transfer (CEST) and spin-locking methods (CESTrho).

    PubMed

    Kogan, Feliks; Singh, Anup; Cai, Keija; Haris, Mohammad; Hariharan, Hari; Reddy, Ravinder

    2012-07-01

    Proton exchange imaging is important as it allows for visualization and quantification of the distribution of specific metabolites with conventional MRI. Current exchange mediated MRI methods suffer from poor contrast as well as confounding factors that influence exchange rates. In this study we developed a new method to measure proton exchange which combines chemical exchange saturation transfer and T(1)(ρ) magnetization preparation methods (CESTrho). We demonstrated that this new CESTrho sequence can detect proton exchange in the slow to intermediate exchange regimes. It has a linear dependence on proton concentration which allows it to be used to quantitatively measure changes in metabolite concentration. Additionally, the magnetization scheme of this new method can be customized to make it insensitive to changes in exchange rate while retaining its dependency on solute concentration. Finally, we showed the feasibility of using CESTrho in vivo. This sequence is able to detect proton exchange at intermediate exchange rates and is unaffected by the confounding factors that influence proton exchange rates thus making it ideal for the measurement of metabolites with exchangeable protons in this exchange regime.

  1. Separation of phycocyanin from Spirulina platensis using ion exchange chromatography.

    PubMed

    Silveira, Silvana Terra; Quines, Luci Kelin de Menezes; Burkert, Carlos André Veiga; Kalil, Susana Juliano

    2008-08-01

    This paper presents the evaluation of some important parameters for the purification of phycocyanin using ion exchange chromatography. The influences of pH and temperature on the equilibrium partition coefficient were investigated to establish the best conditions for phycocyanin adsorption. The equilibrium isotherm for the phycocyanin-resin system was also determined. The separation of phycocyanin using the Q-Sepharose ion exchange resin was evaluated in terms of the pH and elution volume that improved the increase in purity and recovery. The highest partition coefficients were obtained in the pH range from 7.5 to 8.0 at 25 degrees C. Under these conditions the equilibrium isotherm for phycocyanin adsorption was well described by the Langmuir model, attaining a Q (m) of 22.7 mg/mL and K (d) of 3.1 x 10(-2) mg/mL. The best conditions for phycocyanin purification using the ion exchange column were at pH 7.5 with an elution volume of 36 mL, obtaining 77.3% recovery and a 3.4-fold increase in purity.

  2. Evaluation of Elution Parameters for Cesium Ion Exchange Resins

    SciTech Connect

    Burgeson, Ingrid E.; Deschane, Jaquetta R.; Cook, Bryan J.; Blanchard, David L.; Weier, Dennis R.

    2006-08-28

    Cesium ion exchange is one of the planned processes for treating and disposing of waste at the U.S. Department of Energy Hanford Site. Radioactive supernatant liquids from the waste tanks will undergo ultrafiltration, followed by cesium ion exchange using a regenerable organic ion exchange resin. Two resins, SuperLig?644 and a Resorcinol-formaldehyde resin are being evaluated for cesium removal and cesium elution characteristics. The main purpose of this study is to optimize the cesium elution to provide a resin which after undergoing elution would meet the U.S. Department of Energy/Office of River Protection Project-Waste Treatment Plant processing and resin disposal criteria. Columns of each resin type were loaded to greater or equal to 90% breakthrough with a Hanford waste stimulant and eluted with nitric acid. The temperature, flow rate and nitric acid concentration were varied to determine the optimal elution conditions. Temperature and eluant flow rate were the most important elution parameters. As would be predicted based upon kinetic consideration alone, decreasing the eluant flow rate and increasing the temperature provided the optimal elution conditions. Varying the nitric acid concentration did not have a significant effect on the elution; however, elutions performed using both high acid concentration (1M) and elevated temperature (45 C) resulted in resin degradation, causing gas generation and resin bed disruption.

  3. Thermal analysis for ion-exchange column system

    SciTech Connect

    Lee, S. Y.; King, W. D.

    2012-07-01

    Models have been developed to simulate the thermal characteristics of Crystalline Silico-titanate (CST) ion exchange media fully loaded with radioactive cesium in a column configuration and distributed within a waste storage tank. This work was conducted to support the Small Column Ion Exchange (SCIX) program which is focused on processing dissolved, high-sodium salt waste for the removal of specific radionuclides (including Cs-137, Sr-90, and actinides) within a High Level Waste (HLW) storage tank at the Savannah River Site. A two-dimensional computational modeling approach for the in-column ion-exchange domain was taken to include conservative, bounding estimates for key parameters such that the results would provide the maximum centerline temperatures achievable under the design configurations using a feed composition known to promote high cesium loading on CST. A primary objective of these calculations was to estimate temperature distributions across packed CST beds immersed in waste supernate or filled with dry air under various accident scenarios. Accident scenarios evaluated included loss of salt solution flow through the bed, inadvertent column drainage, and loss of active cooling in the column. The modeling results demonstrate that the baseline design using one central and four outer cooling tubes provides a highly efficient cooling mechanism for reducing the maximum column temperature. (authors)

  4. Alkaline aluminum phosphate glasses for thermal ion-exchanged optical waveguide

    NASA Astrophysics Data System (ADS)

    Wang, Fei; Chen, Baojie; Pun, Edwin Yue Bun; Lin, Hai

    2015-04-01

    Alkaline aluminum phosphate glasses (NMAP) with excellent chemical durability for thermal ion-exchanged optical waveguide have been designed and investigated. The transition temperature Tg (470 °C) is higher than the ion-exchange temperature (390 °C), which is favorable to sustain the stability of the glass structure for planar waveguide fabrication. The effective diffusion coefficient De of K+-Na+ ion exchange in NMAP glasses is 0.110 μm2/min, indicating that ion exchange can be achieved efficiently in the optical glasses. Single-mode channel waveguide has been fabricated on Er3+/Yb3+ doped NMAP glass substrate by standard micro-fabrication and K+-Na+ ion exchange. The mode field diameter is 9.6 μm in the horizontal direction and 6.0 μm in the vertical direction, respectively, indicating an excellent overlap with a standard single-mode fiber. Judd-Ofelt intensity parameter Ω2 is 5.47 × 10-20 cm2, implying a strong asymmetrical and covalent environment around Er3+ in the optical glasses. The full width at half maximum and maximum stimulated emission cross section of the 4I13/2 → 4I15/2 are 30 nm and 6.80 × 10-21 cm2, respectively, demonstrating that the phosphate glasses are potential glass candidates in developing compact optoelectronic devices. Pr3+, Tm3+ and Ho3+ doped NMAP glasses are promising candidates to fabricate waveguide amplifiers and lasers operating at special telecommunication windows.

  5. Ion exchange substrates for plant cultivation in extraterrestrial stations and space crafts

    NASA Astrophysics Data System (ADS)

    Soldatov, Vladimir

    2012-07-01

    Ion exchange substrates Biona were specially designed at the Belarus Academy of Sciences for plants cultivation in spacecrafts and extraterrestrial stations. The first versions of such substrates have been successfully used in several space experiments and in a long-term experiment in which three soviet test-spacemen spent a full year in hermetic cabin imitating a lunar station cabin (1067-1968). In this experiment the life support system included a section with about one ton of the ion exchange substrate, which was used to grow ten vegetations of different green cultures used in the food of the test persons. Due to failure of a number of Soviet space experiments, decay of the Soviet Union and the following economic crisis the research in this field carried out in Belarus were re-directed to the needs of usual agriculture, such as adaptation of cell cultures, growing seedlings, rootage of cuttings etc. At present ion exchange substrate Biona are produced in limited amounts at the experimental production plant of the Institute of Physical Organic Chemistry and used in a number of agricultural enterprises. New advanced substrates and technologies for their production have been developed during that time. In the presentation scientific principles of preparation and functioning of ion exchange substrates as well as results of their application for cultivation different plants are described. The ion exchange substrate is a mixture of cation and anion exchangers saturated in a certain proportions with all ions of macro and micro elements. These chemically bound ions are not released to water and become available for plants in exchange to their root metabolites. The substrates contain about 5% mass of nutrient elements far exceeding any other nutrient media for plants. They allow generating 3-5 kg of green biomass per kilogram of substrate without adding any fertilizers; they are sterile by the way of production and can be sterilized by usual methods; allow regeneration

  6. PARAFAC analysis of IBIL spectra from silver ion exchanged glasses

    NASA Astrophysics Data System (ADS)

    Valotto, G.; Cattaruzza, E.; Mardegan, M.; Quaranta, A.

    2017-01-01

    In this work we present for the first time an application of PARAllel FACtor (PARAFAC) analysis to the investigation of Ion Beam Induced Luminescence (IBIL) spectra of Ag+ ↔ Na+ ion exchanged silicate glasses, in order to check the possibility to obtain additional information on the formation of silver aggregates under ion irradiation by a proper statistical rearrangement of experimental spectra. We decomposed the data by PARAFAC taking into account both IBIL emission features and their evolution as a function of the time. Shape and trend under irradiation of the extracted components were correlated to silver concentration and aggregates in the investigated systems. Strength and weakness of this statistical approach applied to IBIL spectra recorded as a function of time were evidenced and discussed.

  7. Metal ion sorption by untreated and chemically treated biomass

    SciTech Connect

    Kilbane, J.J.; Xie, J.

    1992-12-31

    The metal-binding ability of biosorbents is well known; however, in comparison with commercial ion-exchange resins the capacity of biosorbents is low. The purpose of this research was to examine chemically modified biosorbents and biosorbents prepared from microorganisms isolated from extreme environments to determine if significant improvements in metal-binding capacity or biosorbents with unique capabilities could be produced. Chemical treatments examined included acid, alkali, carbon disulfide, phosphorus oxychloride, anhydrous formamide, sodium thiosulfate, sodium chloroacetic acid, and phenylsulfonate. Biosorbents were prepared from microorganisms isolated from pristine and acid mine drainage impacted sites and included heterotrophs, methanotrophs, algae, and sulfate reducers. Chemical modification with carbon disulfide, phosphorous oxychloride, and sodium thiosulfate yielded biosorbents with such as much as 74%, 133%, and 155% improvements, respectively, in metal-binding capacity, but the performance of these chemically modified biosorbents deteriorated upon repeated use. A culture isolated from an acid mine drainage impacted site, IGTM17, exhibits about 3-fold higher metal-binding capacity in comparison with other biosorbents examined in this study. IGTM17 also exhibits superior metal-binding ability at decreased pH or in the presence of interfering common cations in comparison with other biosorbents or some commercially available cation exchange resins. Some biosorbents, such as IGTM5, can bind anions. To our knowledge this is the first demonstration of the ability of biosorbents to bind anions. Moreover, preliminary data indicate that the chemical modification of biosorbents may be capable of imparting the ability to selectively bind certain anions. Further research is needed to optimize conditions for the chemical modification and stabilization of biosorbents.

  8. Implications of using approximate Bloch-McConnell equations in NMR analyses of chemically exchanging systems: application to the electron self-exchange of plastocyanin.

    PubMed

    Hansen, D Flemming; Led, Jens J

    2003-08-01

    enhancement of the nuclear relaxation rates, the paramagnetic chemical shift, the electron relaxation rate, the electron self-exchange rate, and the distances between the nuclei and the paramagnetic metal ion, viz. the Cu2+ ion.

  9. Design of high efficiency fibers for ion exchange and heavy metal removal

    NASA Astrophysics Data System (ADS)

    Dominguez, Lourdes

    Ion exchange materials coated on glass fiber substrates have a number of advantages over the conventional ion exchange beads. These include simplification of the overall synthesis including faster more efficient functionalization and elimination of toxic solvents. Other benefits include the ability to be fabricated in the form of felts, papers, or fabrics, improving media contact efficiency and enhancing both the rates of reaction and regeneration. In addition, physical and mechanical requirements of strength and dimensional stability are achieved by use of glass fiber substrates. Investigations were focused on design of: (1) polymeric cationic exchange fibers and their application for lead and mercury removal, (2) polymeric anionic exchange fibers and their application for arsenate removal, (3) enhancement of anionic fiber selectivity for monovalent ions over divalent ions through bulkier triaklylamine functional groups, and (4) polymeric mercaptyl fibers for the application of arsenite removal. The design and characterization of a cationic exchange fiber is described. Dynamic mode (breakthrough) experiments for calcium, lead, and mercury ion solutions are also presented. The second system consists of the preparation and characterization of anionic exchange fibers with equilibrium adsorption isotherms and dynamic mode kinetic experiments for arsenate removal. Modification of the resin with bulkier functional groups (trimethylamine, triethylamine, tripropylamine, tributylanmine), thereby effecting a change in the selectivity from divalent species to monovalent species, is considered in the separation of nitrates from sulfates. The ability of a thiol group to bind to the highly toxic arsenite ion (as is done in proteins and enzymes) provided the model used to chemically modify and characterize a polyvinyl alcohol mercaptyl fibrous system, coated on a fiberglass substrate, for the purpose of arsenite (As3+) removal from water. Physical/chemical aspects of naturally

  10. Exchange bias in polycrystalline magnetite films made by ion-beam assisted deposition

    SciTech Connect

    Kaur, Maninder; Jiang, Weilin; Qiang, You; Burks, Edward; Liu, Kai; Namavar, Fereydoon; Mccloy, John S.

    2014-11-03

    Iron oxide films were deposited onto Si substrates using ion-beam-assisted deposition. The films were ~300 nm thick polycrystalline magnetite with an average crystallite size of ~6 nm. Additionally, incorporation of significant fractions of argon in the films from ion bombardment is evident from chemical analysis, and Fe/O ratios are lower than expected from pure magnetite. However, Raman spectroscopy and x-ray diffraction both indicate that the films are single-phase magnetite. Since no direct evidence of a second phase could be found, exchange bias likely arises due to defects at grain boundaries, possibly amorphous, creating frustrated spins. Since these samples have such small grains, a large fraction of the material consists of grain boundaries, where spins are highly disordered and reverse independently with external field. The high energy deposition process results in an oxygen-rich, argon-containing magnetite film with low temperature exchange bias due to defects at the high concentration of grain boundaries.

  11. Donnan dialysis with ion-exchange membranes. 3: Diffusion coefficients using ions of different valence

    SciTech Connect

    Miyoshi, Hirofumi

    1999-01-01

    Donnan dialysis with ion-exchange membranes was studied under various kinds of experimental conditions using ions of different valences. The diffusion coefficients (D{sub d}) of various kinds of ions in the ion-exchange membrane were obtained by curve fitting an equation derived from the mass balance to three kinds of Donnan dialytic experiments. It was found that the value of D{sub d}/D{sub s} using D{sub d} of monovalent ions in Donnan dialysis with a set of monovalent feed ions and bivalent driving ions was 1/175, where D{sub s} represents a diffusion coefficient in solution. D{sub s} was calculated from the Nernst-Einstein equation substituted by the ionic conductance of ions at infinite dilution in water. Using D{sub d} of bivalent ions in Donnan dialysis with the same set led to a D{sub d}/D{sub s} value of 1/438. Moreover, using D{sub d} in Donnan dialysis with the same set, the value of D{sub d}/D{sub e} was kept constant at 0.4 (D{sub e} expresses the diffusion coefficient in the membrane when the valences of the feed and driving ions are equal). On the other hand, both D{sub d}/D{sub s} and D{sub d}/D{sub e} using D{sub d} in Donnan dialysis with a set of bivalent feed ions and monovalent driving ions were not constant.

  12. U/Th dating by SHRIMP RG ion-microprobe mass spectrometry using single ion-exchange beads

    USGS Publications Warehouse

    Bischoff, J.L.; Wooden, J.; Murphy, F.; Williams, Ross W.

    2005-01-01

    We present a new analytical method for U-series isotopes using the SHRIMP RG (Sensitive High mass Resolution Ion MicroProbe) mass spectrometer that utilizes the preconcentration of the U-series isotopes from a sample onto a single ion-exchange bead. Ion-microprobe mass spectrometry is capable of producing Th ionization efficiencies in excess of 2%. Analytical precision is typically better than alpha spectroscopy, but not as good as thermal ionization mass spectroscopy (TIMS) and inductively coupled plasma multicollector mass spectrometry (ICP-MS). Like TIMS and ICP-MS the method allows analysis of small samples sizes, but also adds the advantage of rapidity of analysis. A major advantage of ion-microprobe analysis is that U and Th isotopes are analyzed in the same bead, simplifying the process of chemical separation. Analytical time on the instrument is ???60 min per sample, and a single instrument-loading can accommodate 15-20 samples to be analyzed in a 24-h day. An additional advantage is that the method allows multiple reanalyses of the same bead and that samples can be archived for reanalysis at a later time. Because the ion beam excavates a pit only a few ??m deep, the mount can later be repolished and reanalyzed numerous times. The method described of preconcentrating a low concentration sample onto a small conductive substrate to allow ion-microprobe mass spectrometry is potentially applicable to many other systems. Copyright ?? 2005 Elsevier Ltd.

  13. Recent progress and applications of ion-exclusion/ion-exchange chromatography for simultaneous determination of inorganic anions and cations.

    PubMed

    Nakatani, Nobutake; Kozaki, Daisuke; Mori, Masanobu; Tanaka, Kazuhiko

    2012-01-01

    One of the ultimate goals of ion chromatography is to determine both anions and cations found in samples with a single chromatographic run. In the present article, recent progress in ion-exclusion/ion-exchange chromatography for the simultaneous determinations of inorganic anions and cations are reviewed. Firstly, the principle and the control for the simultaneous separation and detection of analyte ions using ion-exclusion/cation-exchange chromatography with a weakly acidic cation-exchange column are outlined. Then, advanced chromatographic techniques in terms of analytical time, selectively and sensitivity are summarized. As a related method, ion-exclusion/anion-exchange chromatography with an anion-exchange column could be used for the simultaneous determination of inorganic nitrogen species, such as ammonium, nitrite and nitrate ions. Their usefulness and applications to water-quality monitoring and related techniques are also described.

  14. Structural Insight into the Ion-Exchange Mechanism of the Sodium/Calcium Exchanger

    SciTech Connect

    Liao, Jun; Li, Hua; Zeng, Weizhong; Sauer, David B.; Belmares, Ricardo; Jiang, Youxing

    2012-06-19

    Sodium/calcium (Na{sup +}/Ca{sup 2+}) exchangers (NCX) are membrane transporters that play an essential role in maintaining the homeostasis of cytosolic Ca{sup 2+} for cell signaling. We demonstrated the Na{sup +}/Ca{sup 2+}-exchange function of an NCX from Methanococcus jannaschii (NCX{_}Mj) and report its 1.9 angstrom crystal structure in an outward-facing conformation. Containing 10 transmembrane helices, the two halves of NCX{_}Mj share a similar structure with opposite orientation. Four ion-binding sites cluster at the center of the protein: one specific for Ca{sup 2+} and three that likely bind Na{sup +}. Two passageways allow for Na{sup +} and Ca{sup 2+} access to the central ion-binding sites from the extracellular side. Based on the symmetry of NCX{_}Mj and its ability to catalyze bidirectional ion-exchange reactions, we propose a structure model for the inward-facing NCX{_}Mj.

  15. Continuous ion exchange separation of zirconium and hafnium

    SciTech Connect

    Begovich, J.M.; Sisson, W.G.

    1981-01-01

    A pressurized continuous annular chromatograph (CAC) has been developed for truly continuous ion exchange preparative separations. This device utilizes a slowly rotating annular bed of sorbent material, fixed multiple feed points, and fixed withdrawal locations. Most of our investigations have been performed with a 28-cm-diam by 60-cm-long CAC, but a larger model has recently been designed and constructed. A detailed study has been made of the separation of copper, nickel, and cobalt components from a simulated carbonate leach liquor of the Caron process for recovering nickel and cobalt from laterite ores. Recent studies have investigated the ion exchange separation of zirconium and hafnium from a sulfate feed solution. Nuclear reactor-grade zirconium, containing < 0.01 wt % hafnium, and hafnium, containing < 1% zirconium, have been continuously prepared using cation exchange resin in the pressurized CAC. This device, because of its continuous feed and product withdrawal, its adaptability to largescale operations, and its ability to separate many components, is expected to make chromatography a more competitive process in the industrial sector.

  16. Kinetic studies of clavulanic acid recovery by ion exchange chromatography.

    PubMed

    Barboza, M; Almeida, R M; Hokka, C O

    2001-01-01

    Clavulanic acid (CA) is a beta-lactamase inhibitor produced by strains of Streptomyces clavuligerus. Nowadays, the combination of CA with amoxycillin is the most successful example of the use of a beta-lactam antibiotic sensitive to beta-lactamases together with an inhibitor of these enzymes. Clavulanic acid is purified from fermentation broth by a series of steps consisting mainly of two-phase separation processes such as liquid-liquid extraction, adsorption or ion-exchange chromatography, among others. Amberlite IRA 400, a strong anion-exchange resin, has a very high adsorption capacity for CA (Mayer et al. 1997). This resin can be pre-treated with NaCl (chloride cycle), to remove selectively only those anions, which are able to displace chloride from the resin or with NaOH (hydroxyl cycle), to remove all species of anions. In order to decide the best operating conditions for CA recovery by ion-exchange resins and then to construct a model of this separation process, batch experiments were conducted using Amberlite IRA 400 in the chloride cycle. These runs were carried out in a 200 ml stirred tank, at two different initial solution pH, 6.2 and 4.0; the temperature was maintained at 10 degrees C and 20 degrees C during adsorption and 30 degrees C during the desorption step. It was possible, on the basis of these batch results, to model the separation process, including the adsorption kinetics, equilibrium data and mass transfer limitations.

  17. Charge Exchange Reaction in Dopant-Assisted Atmospheric Pressure Chemical Ionization and Atmospheric Pressure Photoionization.

    PubMed

    Vaikkinen, Anu; Kauppila, Tiina J; Kostiainen, Risto

    2016-08-01

    The efficiencies of charge exchange reaction in dopant-assisted atmospheric pressure chemical ionization (DA-APCI) and dopant-assisted atmospheric pressure photoionization (DA-APPI) mass spectrometry (MS) were compared by flow injection analysis. Fourteen individual compounds and a commercial mixture of 16 polycyclic aromatic hydrocarbons were chosen as model analytes to cover a wide range of polarities, gas-phase ionization energies, and proton affinities. Chlorobenzene was used as the dopant, and methanol/water (80/20) as the solvent. In both techniques, analytes formed the same ions (radical cations, protonated molecules, and/or fragments). However, in DA-APCI, the relative efficiency of charge exchange versus proton transfer was lower than in DA-APPI. This is suggested to be because in DA-APCI both dopant and solvent clusters can be ionized, and the formed reagent ions can react with the analytes via competing charge exchange and proton transfer reactions. In DA-APPI, on the other hand, the main reagents are dopant-derived radical cations, which favor ionization of analytes via charge exchange. The efficiency of charge exchange in both DA-APPI and DA-APCI was shown to depend heavily on the solvent flow rate, with best efficiency seen at lowest flow rates studied (0.05 and 0.1 mL/min). Both DA-APCI and DA-APPI showed the radical cation of chlorobenzene at 0.05-0.1 mL/min flow rate, but at increasing flow rate, the abundance of chlorobenzene M(+.) decreased and reagent ion populations deriving from different gas-phase chemistry were recorded. The formation of these reagent ions explains the decreasing ionization efficiency and the differences in charge exchange between the techniques. Graphical Abstract ᅟ.

  18. Charge Exchange Reaction in Dopant-Assisted Atmospheric Pressure Chemical Ionization and Atmospheric Pressure Photoionization

    NASA Astrophysics Data System (ADS)

    Vaikkinen, Anu; Kauppila, Tiina J.; Kostiainen, Risto

    2016-08-01

    The efficiencies of charge exchange reaction in dopant-assisted atmospheric pressure chemical ionization (DA-APCI) and dopant-assisted atmospheric pressure photoionization (DA-APPI) mass spectrometry (MS) were compared by flow injection analysis. Fourteen individual compounds and a commercial mixture of 16 polycyclic aromatic hydrocarbons were chosen as model analytes to cover a wide range of polarities, gas-phase ionization energies, and proton affinities. Chlorobenzene was used as the dopant, and methanol/water (80/20) as the solvent. In both techniques, analytes formed the same ions (radical cations, protonated molecules, and/or fragments). However, in DA-APCI, the relative efficiency of charge exchange versus proton transfer was lower than in DA-APPI. This is suggested to be because in DA-APCI both dopant and solvent clusters can be ionized, and the formed reagent ions can react with the analytes via competing charge exchange and proton transfer reactions. In DA-APPI, on the other hand, the main reagents are dopant-derived radical cations, which favor ionization of analytes via charge exchange. The efficiency of charge exchange in both DA-APPI and DA-APCI was shown to depend heavily on the solvent flow rate, with best efficiency seen at lowest flow rates studied (0.05 and 0.1 mL/min). Both DA-APCI and DA-APPI showed the radical cation of chlorobenzene at 0.05-0.1 mL/min flow rate, but at increasing flow rate, the abundance of chlorobenzene M+. decreased and reagent ion populations deriving from different gas-phase chemistry were recorded. The formation of these reagent ions explains the decreasing ionization efficiency and the differences in charge exchange between the techniques.

  19. Treatment of chromium plating process effluents with ion exchange resins.

    PubMed

    Tenório, J A; Espinosa, D C

    2001-01-01

    The surface treatment industry deals with various heavy metals, including the elements Cr, Zn, Ni, Cd, and Cu. Conventional treatments of effluents generate class I solid residue. The aim of this investigation was to study the viability of ion exchange as an alternative process for treatment of rinse water and to determine the efficacy of two ion exchange systems, System 1: "strong" cationic resin-"strong" anionic resin and System 2: "strong" cationic resin-"weak" anionic resin. Commercial resins and solutions taken from rinse tanks of chromium plating companies were used in this investigation. A two-column system, one for the cationic resin and another for the anionic resin, both with 150 ml capacity was mounted. The solution was percolated at a rate of 10 ml/min. The following solutions were used for regeneration of the resins: 2% H2SO4 for the cationic and 4% NaOH for the anionic. The percolated solutions revealed chromium contents of less than 0.25 mg/l, independent of the system used. The "strong" cationic resin-"weak" anionic resin gave excellent regeneration results. The "strong" cationic-"strong" anionic resin presented problems during regeneration, and did not release the retained ions after percolation of 2000 ml of 4% NaOH solution. It is concluded that for this type of treatment, the system composed of "strong" cationic resin and "weak" anionic resin is more appropriate.

  20. Ion Exchange and Solvent Extraction: Supramolecular Aspects of Solvent Exchange Volume 21

    SciTech Connect

    Gloe, Karsten; Tasker, Peter A; Oshima, Tatsuya; Watarai, Hitoshi; Nilsson, Mikael

    2013-01-01

    Preface The theme of supramolecular chemistry (SC), entailing the organization of multiple species through noncovalent interactions, has permeated virtually all aspects of chemical endeavor over the past several decades. Given that the observed behavior of discrete molecular species depends upon their weak interactions with one another and with matrix components, one would have to conclude that SC must indeed form part of the fabric of chemistry itself. A vast literature now serves to categorize SC phenomena within a body of consistent terminology. The word supramolecular itself appears in the titles of dozens of books, several journals, and a dedicated encyclopedia. Not surprisingly, the theme of SC also permeates the field of solvent extraction (SX), inspiring the framework for this volume of Ion Exchange and Solvent Extraction. It is attempted in the six chapters of this volume to identify both how supramolecular behavior occurs and is studied in the context of SX and how SC is influencing the current direction of SX. Researchers and practitioners have long dealt with supramolecular interactions in SX. Indeed, the use of polar extractant molecules in nonpolar media virtually assures that aggregative interactions will dominate the solution behavior of SX. Analytical chemists working in the 1930s to the 1950s with simple mono- and bidentate chelating ligands as extractants noted that extraction of metal ions obeyed complicated mass-action equilibria involving complex stoichiometries. As chemists and engineers developed processes for nuclear and hydrometallurgical applications in the 1950s and 1960s, the preference for aliphatic diluents only enhanced the complexity and supramolecular nature of extraction chemistry. Use of physical techniques such as light scattering and vapor-pressure measurements together with various spectroscopic methods revealed organic-phase aggregates from well-defined dimers to small aggregates containing a few extractant molecules to large

  1. Nitrate and Perchlorate removal from groundwater by ion exchange

    SciTech Connect

    Burge, S; Halden, R

    1999-09-15

    This study was conducted to evaluate the performance of a small scale ion exchange unit (Krudico, Inc of Auborn, IA) for removal of nitrate and perchlorate from groundwater at Lawrence Livermore National Laboratory's Site 300. The unit was able to treat 3,600 gallons of Site 300 groundwater, at an average influent concentration of 100 mg/L NO{sub 3}{sup -} before breakthrough occurred. The unit contained 2.5 ft{sup 3} of Sybron SR-7 resin. Seventy gallons of regeneration waste were generated (water treated to waste ratio of 51:1). The effluent concentration was about 20 mg/L NO{sub 3}{sup -}, which is equivalent to a treatment efficiency of at least 80%. There are several options for implementing this technology at Site 300. A target well, in the 817 area, has been selected. It has a 3 to 4 gpm flow rate, and concentrations of 90 mg/L NO{sub 3}{sup -} and 40 {micro}g/L perchlorate. The different treatment options include ion exchange treatment of nitrate only, nitrate and perchlorate, or perchlorate only. Option 1: For the treatment of nitrate only, this unit will be able to treat 3,700 gallons of water before regeneration is required. If both columns of the ion exchange unit are used, 7,400 gallons could be treated before the columns will need to be regenerated (producing 140 gallons of waste, per cycle or every 1.5 days). The effluent nitrate concentration is expected to be about 17 mg/L. Annual operation and maintenance costs are estimated to be $0.14 per gallon of water treated. Option 2: If only perchlorate is to be removed with ion exchange at the 817 area, a smaller unit should be considered. A 55 gallon canister filled with ion exchange resin should be able to reduce perchlorate concentrations in the groundwater from 40 {micro}g/L to non-detect levels for three years before the resin would need to be replaced. The contaminant-laden resin would be disposed of as hazardous waste. It is not practical to regenerate the resin because of the extreme difficulty of

  2. Ion-Exchange Chromatography: Basic Principles and Application.

    PubMed

    Cummins, Philip M; Rochfort, Keith D; O'Connor, Brendan F

    2017-01-01

    Ion-Exchange Chromatography (IEC) allows for the separation of ionizable molecules on the basis of differences in charge properties. Its large sample-handling capacity, broad applicability (particularly to proteins and enzymes), moderate cost, powerful resolving ability, and ease of scale-up and automation have led to it becoming one of the most versatile and widely used of all liquid chromatography (LC) techniques. In this chapter, we review the basic principles of IEC, as well as the broader criteria for selecting IEC conditions. By way of further illustration, we outline basic laboratory protocols to partially purify a soluble serine peptidase from bovine whole brain tissue, covering crude tissue extract preparation through to partial purification of the target enzyme using anion-exchange chromatography. Protocols for assaying total protein and enzyme activity in both pre- and post-IEC fractions are also described.

  3. Ion exchange and adsorption on low rank coals for liquefaction

    SciTech Connect

    Vorres, K.S.

    1994-09-01

    The objectives of this program are to study the application of catalysts and the catalysis of liquefaction of low rank coals. Ion exchange and adsorption techniques are being used or modified to incorporate catalytically active metals (Fe, Co, Ni and Mo) in relatively small (100-2000 ppM) quantities into coal samples. Relative oil yields are being determined by PETC and Auburn University workers as collaborators to establish the effectiveness of the catalyst incorporation techniques. It is hoped that these techniques will provide highly active forms of the catalyst in low concentrations to minimize the need for metals recovery. A two step preparation of the coal is used to (1) remove material which both limits oil conversion and prepares for the addition of exchangeable catalyst, and (2) add catalytically active material which enhances the conversion of the coal matter to the oil fraction in the processing.

  4. Ion-exchange equilibrium of N-acetyl-D-neuraminic acid on a strong anionic exchanger.

    PubMed

    Wu, Jinglan; Ke, Xu; Zhang, Xudong; Zhuang, Wei; Zhou, Jingwei; Ying, Hanjie

    2015-09-15

    N-acetyl-D-neuraminic acid (Neu5Ac) is a high value-added product widely applied in the food industry. A suitable equilibrium model is required for purification of Neu5Ac based on ion-exchange chromatography. Hence, the equilibrium uptake of Neu5Ac on a strong anion exchanger, AD-1 was investigated experimentally and theoretically. The uptake of Neu5Ac by the hydroxyl form of the resin occurred primarily by a stoichiometric exchange of Neu5Ac(-) and OH(-). The experimental data showed that the selectivity coefficient for the exchange of Neu5Ac(-) with OH(-) was a non-constant quantity. Subsequently, the Saunders' model, which took into account the dissociation reactions of Neu5Ac and the condition of electroneutrality, was used to correlate the Neu5Ac sorption isotherms at various solution pHs and Neu5Ac concentrations. The model provided an excellent fit to the binary exchange data for Cl(-)/OH(-) and Neu5Ac(-)/OH(-), and an approximate prediction of equilibrium in the ternary system Cl(-)/Neu5Ac(-)/OH(-). This basic information combined with the general mass transfer model could lay the foundation for the prediction of dynamic behavior of fixed bed separation process afterwards.

  5. Ion Exchange Testing with SRF Resin FY2012

    SciTech Connect

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

    2013-06-11

    Ion exchange using spherical resorcinol-formaldehyde (SRF) resin has been selected by the U.S. Department of Energy’s Office of River Protection (DOE-ORP) for use in the Pretreatment Facility (PTF) of the Hanford Tank Waste Treatment and Immobilization Plant (WTP) and for potential application in at-tank deployment. Numerous studies have shown SRF resin to be effective for removing 137Cs from a wide variety of actual and simulated tank waste supernatants (Adamson et al. 2006; Blanchard et al. 2008; Burgeson et al. 2004; Duignan and Nash 2009; Fiskum et al. 2006a; Fiskum et al. 2006b; Fiskum et al. 2006c; Fiskum et al. 2007; Hassan and Adu-Wusu 2003; King et al. 2004; Nash et al. 2006). Prior work at the Pacific Northwest National Laboratory (PNNL) has focused primarily on the loading behavior for 4 to 6 M Na solutions at 25 to 45°C. Recent proposed changes to the WTP ion exchange process baseline indicate that loading may include a broader range of sodium molarities (0.1 to 8 M) and higher temperatures (50°C) to alleviate post-filtration precipitation issues. This report discusses ion exchange loading kinetics testing activities performed in accordance with Test Plan TP-WTPSP-002, Rev. 3.0 , which was prepared and approved in response to the Test Specification 24590 PTF-TSP-RT-09-002, Rev. 0 (Lehrman 2010) and Test Exception 24590 PTF TEF RT-11-00003, Rev. 0 (Meehan 2011). This testing focused on column tests evaluating the impact of elevated temperature on resin degradation over an extended period of time and batch contacts evaluating the impact on Cs loading over a broad range of sodium concentrations (0.1 to 5 M). These changes may be required to alleviate post-filtration precipitation issues and broaden the data range of SRF resin loading under the conditions expected with the new equipment and process changes.

  6. Vitrification of cesium-contaminated organic ion exchange resin

    SciTech Connect

    Sargent, Jr., Thomas N.

    1994-08-01

    Vitrification has been declared by the Environmental Protection Agency (USEPA) as the Best Demonstrated Available Technology (BDAT) for the permanent disposal of high-level radioactive waste. Savannah River Site currently uses a sodium tetraphenylborate (NaTPB) precipitation process to remove Cs-137 from a wastewater solution created from the processing of nuclear fuel. This process has several disadvantages such as the formation of a benzene waste stream. It has been proposed to replace the precipitation process with an ion exchange process using a new resorcinol-formaldehyde resin developed by Savannah River Technical Center (SRTC). Preliminary tests, however, showed that problems such as crust formation and a reduced final glass wasteform exist when the resin is placed in the melter environment. The newly developed stirred melter could be capable of overcoming these problems. This research explored the operational feasibility of using the stirred tank melter to vitrify an organic ion exchange resin. Preliminary tests included crucible studies to determine the reducing potential of the resin and the extent of oxygen consuming reactions and oxygen transfer tests to approximate the extent of oxygen transfer into the molten glass using an impeller and a combination of the impeller and an external oxygen transfer system. These preliminary studies were used as a basis for the final test which was using the stirred tank melter to vitrify nonradioactive cesium loaded organic ion exchange resin. Results from this test included a cesium mass balance, a characterization of the semi-volatile organic compounds present in the off gas as products of incomplete combustion (PIC), a qualitative analysis of other volatile metals, and observations relating to the effect the resin had on the final redox state of the glass.

  7. HEAT TRANSFER ANALYSIS FOR ION-EXCHANGE COLUMN SYSTEM

    SciTech Connect

    Lee, S.; King, W.

    2011-05-23

    Models have been developed to simulate the thermal characteristics of Crystalline Silicotitanate (CST) ion exchange media fully loaded with radioactive cesium in a column configuration and distributed within a waste storage tank. This work was conducted to support the Small Column Ion Exchange (SCIX) program which is focused on processing dissolved, high-sodium salt waste for the removal of specific radionuclides (including Cs-137, Sr-90, and actinides) within a High Level Waste (HLW) storage tank at the Savannah River Site. The SCIX design includes CST columns inserted and supported in the tank top risers for cesium removal. Temperature distributions and maximum temperatures across the column were calculated with a focus on process upset conditions. A two-dimensional computational modeling approach for the in-column ion-exchange domain was taken to include conservative, bounding estimates for key parameters such that the results would provide the maximum centerline temperatures achievable under the design configurations using a feed composition known to promote high cesium loading on CST. The current full-scale design for the CST column includes one central cooling pipe and four outer cooling tubes. Most calculations assumed that the fluid within the column was stagnant (i.e. no buoyancy-induced flow) for a conservative estimate. A primary objective of these calculations was to estimate temperature distributions across packed CST beds immersed in waste supernate or filled with dry air under various accident scenarios. Accident scenarios evaluated included loss of salt solution flow through the bed, inadvertent column drainage, and loss of active cooling in the column. The modeling results demonstrate that the baseline design using one central and four outer cooling tubes provides a highly efficient cooling mechanism for reducing the maximum column temperature.

  8. Solid Phase Luminescence of Several Rare Earth Ions on Ion-Exchange Films

    NASA Technical Reports Server (NTRS)

    Tanner, Stephen P.; Street, Kenneth W., Jr.

    1999-01-01

    The development and characterization of a novel ion-exchange film for solid-phase fluorometry and phosphorimetry is reported. This new cation-exchange material is suitable for spectroscopic applications in the ultraviolet and visible regions. It is advantageous because it, as a single entity, is easily recovered from solution and mounted in the spectrofluorometers. After preconcentration on the film, the luminescence intensity of lanthanide ions is several orders of magnitude greater than that of the corresponding solution, depending on the volume of solution and the amount of film. This procedure allows emission spectral measurements and determination of lanthanide ions at solution concentrations of < 5 (micro)g/L. The film may be stored for subsequent reuse or as a permanent record of the analysis. The major drawback to the use of the film is slow uptake of analyte due to diffusion limitations.

  9. Regeneration of spent powdered activated carbon saturated with inorganic ions by cavitation united with ion exchange method.

    PubMed

    Li, Gang; Gao, Hong; Li, Yansheng; Yang, Huixin

    2011-06-01

    Using ion exchange resin as transfer media, regenerate powdered activated carbon (PAC) adsorbed inorganic ions by cavitation to enhance the transfer; we studied how the regeneration time and the mass ratio of resin and PAC influence the regeneration rate respectively through re-adsorption. The result showed that the effective regeneration of PAC saturated with inorganic ions was above 90% using ion exchange resin as media and transfer carrier, the quantity of PAC did not reduced but activated in the process.

  10. Molecular simulations of ion exchange in NaA zeolite membranes

    NASA Astrophysics Data System (ADS)

    Murad, S.; Jia, W.; Krishnamurthy, M.

    2003-02-01

    Molecular simulations using the method of molecular dynamics have been carried out to determine the possibility of studying ion exchanges between electrolyte solutions (here an aqueous LiCl solution) and an ion-exchange membrane (NaA zeolite) using direct simulations of upto a nanosecond. Our results show that with appropriate driving forces, such ion-exchange processes can be clearly witnessed and investigated using molecular simulations. We have also attempted to understand the phenomenon at the molecular level. Our results have shown that the ion-exchange process is energetically driven and entropic forces are not playing any significant role in the exchanges observed.

  11. Ion exchange of ammonium in natural and synthesized zeolites.

    PubMed

    Wang, Yifei; Lin, Feng; Pang, Wenqin

    2008-12-30

    In this study, zeolite Na-P and Na-Y was prepared by hydrothermal treatment of the Chinese natural clinoptilolite with NaOH. The ion exchange of NH4+ into the three zeolites in the temperature range of 288-333K was also investigated, and the thermodynamic parameters were calculated. The selectivity sequence for NH4+ entering the sodium form of the three materials was Na-clinoptilolite>Na-Y>Na-P, as indicated by values of DeltaG degrees . The results demonstrated that the Si/Al molar ratio of zeolites determined the selectivity for NH4+.

  12. Effect of calcium/sodium ion exchange on the osmotic properties and structure of polyelectrolyte gels.

    PubMed

    Horkay, Ferenc; Basser, Peter J; Hecht, Anne-Marie; Geissler, Erik

    2015-12-01

    We discuss the main findings of a long-term research program exploring the consequences of sodium/calcium ion exchange on the macroscopic osmotic and elastic properties, and the microscopic structure of representative synthetic polyelectrolyte (sodium polyacrylate, (polyacrylic acid)) and biopolymer gels (DNA). A common feature of these gels is that above a threshold calcium ion concentration, they exhibit a reversible volume phase transition. At the macroscopic level, the concentration dependence of the osmotic pressure shows that calcium ions influence primarily the third-order interaction term in the Flory-Huggins model of polymer solutions. Mechanical tests reveal that the elastic modulus is practically unaffected by the presence of calcium ions, indicating that ion bridging does not create permanent cross-links. At the microscopic level, small-angle neutron scattering shows that polyacrylic acid and DNA gels exhibit qualitatively similar structural features in spite of important differences (e.g. chain flexibility and chemical composition) between the two polymers. The main effect of calcium ions is that the neutron scattering intensity increases due to the decrease in the osmotic modulus. At the level of the counterion cloud around dissolved macroions, anomalous small-angle X-ray scattering measurements made on DNA indicate that divalent ions form a cylindrical sheath enveloping the chain, but they are not localized. Small-angle neutron scattering and small-angle X-ray scattering provide complementary information on the structure and interactions in polymer solutions and gels.

  13. FDM study of ion exchange diffusion equation in glass

    NASA Astrophysics Data System (ADS)

    Zhou, Zigang; Yang, Yongjia; Wang, Qiang; Sun, Guangchun

    2009-05-01

    Ion-exchange technique in glass was developed to fabricate gradient refractive index optical devices. In this paper, the Finite Difference Method(FDM), which is used for the solution of ion-diffusion equation, is reported. This method transforms continual diffusion equation to separate difference equation. It unitizes the matrix of MATLAB program to solve the iteration process. The collation results under square boundary condition show that it gets a more accurate numerical solution. Compared to experiment data, the relative error is less than 0.2%. Furthermore, it has simply operation and kinds of output solutions. This method can provide better results for border-proliferation of the hexagonal and the channel devices too.

  14. ION EXCHANGE SUBSTANCES BY SAPONIFICATION OF ALLYL PHOSPHATE POLYMERS

    DOEpatents

    Kennedy, J.

    1959-04-14

    An ion exchange resin having a relatively high adsorption capacity tor uranyl ion as compared with many common cations is reported. The resin comprises an alphyl-allyl hydrogen phosphate polymer, the alphyl group being either allyl or a lower alkyl group having up to 5 carbon atoins. The resin is prepared by polymerizing compounds such as alkyl-diallyl phosphate and triallyl phosphate in the presence of a free radical generating substance and then partially hydrolyzing the resulting polymer to cause partial replacement of organic radicals by cations. A preferred free radical gencrating agent is dibenzoyl peroxide. The partial hydrolysis is brought about by refluxing the polymer with concentrated aqueous NaOH for three or four hours.

  15. Extraction and ion-exchange behavior of mendelevium (II)

    SciTech Connect

    Guseva, L.I.; Tikhomirova, G.S.; Buklanov, G.V.; Pkhar, Z.Z.; Lebedev, I.A.; Katargin, N.V.; Myasoedov, B.F.

    1988-09-01

    Medelevium-256 was obtained via multinucleon transfer reactions upon irradiation of /sup 249/Bk by /sup 22/Ne ions from the extracted beam of a U-300 cyclotron. In order to extract mendelevium and separate it from the products of nuclear reactions, an express ion-exchange method using one column with cationite and zinc amalgam in a solution of 1 mole/liter HCl as the eluent was developed. It was shown that under these conditions mendelevium is reduced and washes out as an alkaline earth element. On the basis of the location of the peaks of the elution curves of Sr/sup 2+/, Eu/sup 2+/, and Md/sup 2+/, the value of the ionic radium of Md/sup 2+/ is estimated and is used to estimate the heat of hydration.

  16. New Charge Exchange Calculations for Lowly-Charged Ions

    NASA Astrophysics Data System (ADS)

    Stancil, P. C.

    2005-05-01

    The process of charge exchange, which occurs during the collision of an ion with a neutral species, is important in a variety of astrophysical and atmospheric environments. It can have an influence on the ionization and thermal balances of the plasma and may also contribute to the emission spectrum. The charge exchange of multiply-charged ions (q>2) usually proceeds at a fast rate with rate coefficients typically of 10-10 to 10-9 cm3s-1. Therefore, highly-charged ions, which are created in UV or x-ray ionized gas, quickly recombine to smaller charges. However, the rate coefficients for singly- and doubly-charged ions can vary over five orders of magnitude depending on the ion species, the neutral target, and the temperature. In particular, the rate coefficients depend sensitively on the dominant mechanism which may be due to radial, rotational, radiative, or spin-orbit coupling and the corresponding quasi-molecular curves can be very complicated. Measurements of such processes are complicated by metastable contamination and uncertainties in target purity and estimates of empirical values inferred from astrophysical modeling are typically suspect. Therefore, the state of knowledge of lowly-charged electron transfer processes is generally poor, but these reactions can be critical in determining the state of the plasma. If, for example, the rate coefficient for a q=2 ion is very small, the process would result in a bottle-neck in the recombination cascade from higer charges. In an effort to address these problems, quantum-mechanical calculations have been carried out for a number of singly- and doubly-charged ions and benchmarked to measurements when available. I will present a summary of these results which reveal significant differences from values adopted in rate coefficient compilations used by various modeling packages. This work was performed in collaboration with L. B. Zhao, C. Y. Lin, J. P. Gu, H. P. Liebermann, R. J. Buenker, and M. Kimura. Support from NASA

  17. Effects of ion exchange resins in different mobile ion forms on semi-aerobic landfill leachate treatment.

    PubMed

    Bashir, Mohammed J K; Aziz, Hamidi Abdul; Yusoff, Mohd Suffian; Huqe, A A M; Mohajeri, Soraya

    2010-01-01

    Landfill leachate is one of the major contamination sources. In this study, the ability of synthetic ion exchange resins which carry different mobile ion for removing color, chemical oxygen demand (COD), and ammonia nitrogen (NH(3)-N) from stabilized leachate was investigated. The synthetic resin INDION 225 Na as a cationic exchanger and INDION FFIP MB as an anionic exchanger were used in this study. INDION 225 Na was used in hydrogen form (H(+)) and in sodium form (Na(+)), while INDION FFIP MB resin was used in hydroxide form (OH(-)) and in calcium form (Cl(-)) form. The results indicated better removal of color, COD and NH(3)-N by using INDION 225 Na in H(+) as compared with Na(+) form, while no performance differences were observed by using INDION FFIP MB in OH(-) or Cl(-) form. Applying cationic resin followed by anionic resin achieved 97, 88 and 94, percent removal of color, COD and NH(3)-N. The residual amounts were 160 Pt-Co, 290 mg/L and 110 mg/L of color, COD and NH(3)-N respectively.

  18. Partitioning of mobile ions between ion exchange polymers and aqueous salt solutions: importance of counter-ion condensation.

    PubMed

    Kamcev, Jovan; Galizia, Michele; Benedetti, Francesco M; Jang, Eui-Soung; Paul, Donald R; Freeman, Benny D; Manning, Gerald S

    2016-02-17

    Equilibrium partitioning of ions between a membrane and a contiguous external solution strongly influences transport properties of polymeric membranes used for water purification and energy generation applications. This study presents a theoretical framework to quantitatively predict ion sorption from aqueous electrolytes (e.g., NaCl, MgCl2) into charged (i.e., ion exchange) polymers. The model was compared with experimental NaCl, MgCl2, and CaCl2 sorption data in commercial cation and anion exchange membranes. Ion sorption in charged polymers was modeled using a thermodynamic approach based on Donnan theory coupled with Manning's counter-ion condensation theory to describe non-ideal behavior of ions in the membrane. Ion activity coefficients in solution were calculated using the Pitzer model. The resulting model, with no adjustable parameters, provides remarkably good agreement with experimental values of membrane mobile salt concentration. The generality of the model was further demonstrated using literature data for ion sorption of various electrolytes in charged polymers, including HCl sorption in Nafion.

  19. Tailoring orthogonal proteomic routines to understand protein separation during ion exchange chromatography.

    PubMed

    Cabrera, Rosa; Zhelyazkova, Petya; Galvis, Leonardo; Fernandez-Lahore, Marcelo

    2008-07-01

    Surface charge, molecular weight, and folding state are known to influence protein chromatographic behaviour onto ion exchangers. Experimentally, information related to such factors can be gathered via 2-DE methods. The application of 2-D PAGE under denaturing/reducing conditions was already shown to reveal separation trends within a large protein population from cell extracts. However, ion-exchange chromatography normally runs under native conditions. A tailored protocol consisting in a first separation based on IEF on Immobiline strips under native conditions followed by a second dimension SDS-PAGE run was adopted. The chromatographic versus electrophoretic separation behaviours of two model proteins, thaumatin (TAU) and BSA, were compared to better understand which proteomic routine would be better suited to anticipate IEX chromatographic separations. It was observed that the information contained in the pI value obtained with the adapted 2-DE protocol showed better correlation with the IEX chromatographic behaviour. On the other hand, chromatographic separations performed in the presence of urea as a denaturant have demonstrated the potential influence of hydrodynamic radius/conformation on protein separation. Moreover, the information provided by such 2-D system correlated well with the chromatographic behaviour of an additional set of pure proteins. An initial prediction of protein ion-exchange chromatographic behaviour could be possible utilizing an experimental approach based on 2-DE running under milder chemical conditions. This technique provides information that more closely resembles the separation behaviour observed with a complex biotechnological feedstock.

  20. Factorial experimental design for recovering heavy metals from sludge with ion-exchange resin.

    PubMed

    Lee, I Hsien; Kuan, Yu-Chung; Chern, Jia-Ming

    2006-12-01

    Wastewaters containing heavy metals are usually treated by chemical precipitation method in Taiwan. This method can remove heavy metals form wastewaters efficiently, but the resultant heavy metal sludge is classified as hazardous solid waste and becomes another environmental problem. If we can remove heavy metals from sludge, it becomes non-hazardous waste and the treatment cost can be greatly reduced. This study aims at using ion-exchange resin to remove heavy metals such as copper, zinc, cadmium, and chromium from sludge generated by a PCB manufacturing plant. Factorial experimental design methodology was used to study the heavy metal removal efficiency. The total metal concentrations in the sludge, resin, and solution phases were measured respectively after 30 min reaction with varying leaching agents (citric acid and nitric acid); ion-exchange resins (Amberlite IRC-718 and IR-120), and temperatures (50 and 70 degrees C). The experimental results and statistical analysis show that a stronger leaching acid and a higher temperature both favor lower heavy metal residues in the sludge. Two-factors and even three-factor interaction effects on the heavy metal sorption in the resin phase are not negligible. The ion-exchange resin plays an important role in the sludge extraction or metal recovery. Empirical regression models were also obtained and used to predict the heavy metal profiles with satisfactory results.

  1. Increasing parvovirus filter throughput of monoclonal antibodies using ion exchange membrane adsorptive pre-filtration.

    PubMed

    Brown, Arick; Bechtel, Charity; Bill, Jerome; Liu, Hui; Liu, Jun; McDonald, Dan; Pai, Satyan; Radhamohan, Asha; Renslow, Ryan; Thayer, Brooke; Yohe, Stefan; Dowd, Chris

    2010-07-01

    Pre-filtration using ion exchange membrane adsorbers can improve parvovirus filter throughput of monoclonal antibodies (mAbs). The membranes work by binding trace foulants, and although some antibody product also binds, yields > or =99% are easily achieved by overloading. Results show that foulant adsorption is dependent on pH and conductivity, but independent of scale and adsorber brand. The ability to use ion exchange membranes as pre-filters is significant because it provides a clean, well defined, chemically stable option for enhancing throughput. Additionally, ion exchange membranes facilitate characterization of parvovirus filter foulants. Examination of adsorber elution samples using sedimentation velocity analysis and SEC-MALS/QELS revealed the presence of high molecular weight species ranging from 8 to 13 nm in hydrodynamic radius, which are similar in size to parvoviruses and thus would be expected to plug the pores of a parvovirus filter. A study of two identical membranes in-series supports the hypothesis that the foulants are soluble, trace level aggregates in the feed. This study's significance lies in a previously undiscovered application of membrane chromatography, leading to a more cost effective and robust approach to parvovirus filtration for the production of monoclonal antibodies.

  2. Unified superresolution experiments and stochastic theory provide mechanistic insight into protein ion-exchange adsorptive separations

    PubMed Central

    Kisley, Lydia; Chen, Jixin; Mansur, Andrea P.; Shuang, Bo; Kourentzi, Katerina; Poongavanam, Mohan-Vivekanandan; Chen, Wen-Hsiang; Dhamane, Sagar; Willson, Richard C.; Landes, Christy F.

    2014-01-01

    Chromatographic protein separations, immunoassays, and biosensing all typically involve the adsorption of proteins to surfaces decorated with charged, hydrophobic, or affinity ligands. Despite increasingly widespread use throughout the pharmaceutical industry, mechanistic detail about the interactions of proteins with individual chromatographic adsorbent sites is available only via inference from ensemble measurements such as binding isotherms, calorimetry, and chromatography. In this work, we present the direct superresolution mapping and kinetic characterization of functional sites on ion-exchange ligands based on agarose, a support matrix routinely used in protein chromatography. By quantifying the interactions of single proteins with individual charged ligands, we demonstrate that clusters of charges are necessary to create detectable adsorption sites and that even chemically identical ligands create adsorption sites of varying kinetic properties that depend on steric availability at the interface. Additionally, we relate experimental results to the stochastic theory of chromatography. Simulated elution profiles calculated from the molecular-scale data suggest that, if it were possible to engineer uniform optimal interactions into ion-exchange systems, separation efficiencies could be improved by as much as a factor of five by deliberately exploiting clustered interactions that currently dominate the ion-exchange process only accidentally. PMID:24459184

  3. Unified superresolution experiments and stochastic theory provide mechanistic insight into protein ion-exchange adsorptive separations.

    PubMed

    Kisley, Lydia; Chen, Jixin; Mansur, Andrea P; Shuang, Bo; Kourentzi, Katerina; Poongavanam, Mohan-Vivekanandan; Chen, Wen-Hsiang; Dhamane, Sagar; Willson, Richard C; Landes, Christy F

    2014-02-11

    Chromatographic protein separations, immunoassays, and biosensing all typically involve the adsorption of proteins to surfaces decorated with charged, hydrophobic, or affinity ligands. Despite increasingly widespread use throughout the pharmaceutical industry, mechanistic detail about the interactions of proteins with individual chromatographic adsorbent sites is available only via inference from ensemble measurements such as binding isotherms, calorimetry, and chromatography. In this work, we present the direct superresolution mapping and kinetic characterization of functional sites on ion-exchange ligands based on agarose, a support matrix routinely used in protein chromatography. By quantifying the interactions of single proteins with individual charged ligands, we demonstrate that clusters of charges are necessary to create detectable adsorption sites and that even chemically identical ligands create adsorption sites of varying kinetic properties that depend on steric availability at the interface. Additionally, we relate experimental results to the stochastic theory of chromatography. Simulated elution profiles calculated from the molecular-scale data suggest that, if it were possible to engineer uniform optimal interactions into ion-exchange systems, separation efficiencies could be improved by as much as a factor of five by deliberately exploiting clustered interactions that currently dominate the ion-exchange process only accidentally.

  4. Filtration and ion exchange trailer system (F.I.T.S.)

    SciTech Connect

    Plante, P.; Pratte, S.; Jenson, C.

    1995-05-01

    In preparation for the fall 1992 outage, Maine Yankee determined that a number of its planned filtration and ion exchange activities would require supplementary equipment not available in the plant. A review of outage processing needs, as well as future requirements, led Maine Yankee to determine that a mobile trailer containing a number of process systems could be (1) moved, as necessary, to various sites around the plant, and (2) easily stored on site between outages. In late spring of 1993, Diversified Technologies was awarded a contract for a Filtration and Ion Exchange Trailer (F.I.T.S.), to be delivered in late summer in preparation for the outage. The trailer contained a multi-media deep bed filter and associated piping and flush tank, a tri-bag filter unit, dual demineralizers, a chemical addition tank and metering pump, static mixer, plant utility interface connections and other instrumentation and controls to permit filtering and ion exchanging the process stream in a variety of configurations. This paper discusses the design criteria, seismic considerations and operational requirements of the mobile trailer. Data and operating experience from full-scale outage operation is reviewed, including desludging of stream generators and dechromating of secondary systems.

  5. Double agents and secret agents: the emerging fields of exogenous chemical exchange saturation transfer and T2-exchange magnetic resonance imaging contrast agents for molecular imaging.

    PubMed

    Daryaei, Iman; Pagel, Mark D

    2015-01-01

    Two relatively new types of exogenous magnetic resonance imaging contrast agents may provide greater impact for molecular imaging by providing greater specificity for detecting molecular imaging biomarkers. Exogenous chemical exchange saturation transfer (CEST) agents rely on the selective saturation of the magnetization of a proton on an agent, followed by chemical exchange of a proton from the agent to water. The selective detection of a biomarker-responsive CEST signal and an unresponsive CEST signal, followed by the ratiometric comparison of these signals, can improve biomarker specificity. We refer to this improvement as a "double-agent" approach to molecular imaging. Exogenous T2-exchange agents also rely on chemical exchange of protons between the agent and water, especially with an intermediate rate that lies between the slow exchange rates of CEST agents and the fast exchange rates of traditional T1 and T2 agents. Because of this intermediate exchange rate, these agents have been relatively unknown and have acted as "secret agents" in the contrast agent research field. This review exposes these secret agents and describes the merits of double agents through examples of exogenous agents that detect enzyme activity, nucleic acids and gene expression, metabolites, ions, redox state, temperature, and pH. Future directions are also provided for improving both types of contrast agents for improved molecular imaging and clinical translation. Therefore, this review provides an overview of two new types of exogenous contrast agents that are becoming useful tools within the armamentarium of molecular imaging.

  6. Double agents and secret agents: the emerging fields of exogenous chemical exchange saturation transfer and T2-exchange magnetic resonance imaging contrast agents for molecular imaging

    PubMed Central

    Daryaei, Iman; Pagel, Mark D

    2016-01-01

    Two relatively new types of exogenous magnetic resonance imaging contrast agents may provide greater impact for molecular imaging by providing greater specificity for detecting molecular imaging biomarkers. Exogenous chemical exchange saturation transfer (CEST) agents rely on the selective saturation of the magnetization of a proton on an agent, followed by chemical exchange of a proton from the agent to water. The selective detection of a biomarker-responsive CEST signal and an unresponsive CEST signal, followed by the ratiometric comparison of these signals, can improve biomarker specificity. We refer to this improvement as a “double-agent” approach to molecular imaging. Exogenous T2-exchange agents also rely on chemical exchange of protons between the agent and water, especially with an intermediate rate that lies between the slow exchange rates of CEST agents and the fast exchange rates of traditional T1 and T2 agents. Because of this intermediate exchange rate, these agents have been relatively unknown and have acted as “secret agents” in the contrast agent research field. This review exposes these secret agents and describes the merits of double agents through examples of exogenous agents that detect enzyme activity, nucleic acids and gene expression, metabolites, ions, redox state, temperature, and pH. Future directions are also provided for improving both types of contrast agents for improved molecular imaging and clinical translation. Therefore, this review provides an overview of two new types of exogenous contrast agents that are becoming useful tools within the armamentarium of molecular imaging. PMID:27747191

  7. Numerical simulation of advective-dispersive multisolute transport with sorption, ion exchange and equilibrium chemistry

    USGS Publications Warehouse

    Lewis, F.M.; Voss, C.I.; Rubin, Jacob

    1986-01-01

    A model was developed that can simulate the effect of certain chemical and sorption reactions simultaneously among solutes involved in advective-dispersive transport through porous media. The model is based on a methodology that utilizes physical-chemical relationships in the development of the basic solute mass-balance equations; however, the form of these equations allows their solution to be obtained by methods that do not depend on the chemical processes. The chemical environment is governed by the condition of local chemical equilibrium, and may be defined either by the linear sorption of a single species and two soluble complexation reactions which also involve that species, or binary ion exchange and one complexation reaction involving a common ion. Partial differential equations that describe solute mass balance entirely in the liquid phase are developed for each tenad (a chemical entity whose total mass is independent of the reaction process) in terms of their total dissolved concentration. These equations are solved numerically in two dimensions through the modification of an existing groundwater flow/transport computer code. (Author 's abstract)

  8. Radiation stability of sodium titanate ion exchange materials

    SciTech Connect

    Kenna, B.T.

    1980-02-01

    Sodium titanate and sodium titanate loaded macroreticular resin are being considered as ion exchangers to remove /sup 90/Sr and actinides from the large volume of defense waste stored at Hanford Site in Washington. Preliminary studies to determine the radiation effect on Sr/sup +2/ and I/sup -/ capacity of these ion-exchange materials were conducted. Samples of sodium titanate powder, sodium titanate loaded macroreticular resin, as well as the nitrate form of macroreticular anion resin were irradiated with up to 2 x 10/sup 9/ Rads of /sup 60/Co gamma rays. Sodium titanate cation capacity decreased about 50% while the sodium titanate loaded macroeticular resin displayed a dramatic decrease in cation capacity when irradiated with 10/sup 8/-10/sup 9/ Rad. The latter decrease is tentatively ascribed to radiation damage to the organic portion which subsequently inhibits interaction with the contained sodium titanate. The anion capacity of both macroreticular resin and sodium titanate loaded macroreticular resin exhibited significant decreases with increasing radiation exposure. These results suggest that consideration should be given to the potential effects of radiation degradation if column regeneration is to be used. 5 figures, 2 tables.

  9. Ion exchangers in radioactive waste management: natural Iranian zeolites.

    PubMed

    Nilchi, A; Maalek, B; Khanchi, A; Ghanadi Maragheh, M; Bagheri, A; Savoji, K

    2006-01-01

    Five samples of natural zeolites from different parts of Iran were chosen for this study. In order to characterize and determine their structures, X-ray diffraction and infrared spectrometry were carried out for each sample. The selective absorption properties of each zeolite were found by calculating the distribution coefficient (K(d)) of various simulated wastes which were prepared by spiking the radionuclides with (131)I, (99)Mo, (153)Sm, (140)La and (147)Nd. All the zeolite samples used in this study had extremely high absorption value towards (140)La; clinoptolite from Mianeh and analsite from Ghalehkhargoshi showed good absorption for (147)Nd; clinoptolite from Semnan and clinoptolite from Firozkoh showed high absorption for (153)Sm; mesolite from Arababad Tabas showed good absorption for (99)Mo; and finally mesolite from Arababad Tabas, clinoptolite from Semnan and clinoptolite from Firozkoh could be used to selectively absorb (131)I from the stimulated waste which was prepared. The natural zeolites chosen for these studies show a similar pattern to those synthetic ion exchangers in the literature and in some cases an extremely high selectivity towards certain radioactive elements. Hence the binary separation of radioactive elements could easily be carried out. Furthermore, these zeolites, which are naturally occurring ion exchangers, are viable economically and extremely useful alternatives in this industry.

  10. Ion exchange at TNX using the SKID unit

    SciTech Connect

    Meyer, M.L.; Bibler, J.P.

    1993-10-21

    An ion exchange unit has been manufactured for WSRC by British Nuclear Fuels, Ltd. This unit consists of three columns, ancillary valving, pumps, lines, and computer controls. It has been delivered to TNX for use in testing a cesium-specific ion exchange resin, developed at WSRC as a potential second generation process for the decontamination of Defense Waste Processing Facility (DWPF) supernate. This resin also has Department of Energy applications at both Oak Ridge and Hanford. Oak Ridge is interested in decontaminating the Melton Valley storage tank supernate, while Hanford is interested in decontaminating the 101-AW and 101-SY supernate streams. Another potential developmental interest is the Savannah River Site (SRS) DWPF recycle stream. The three primary waste streams of interest are the Oak Ridge, Hanford, and SRS, SWPF supernate streams. For these three waste streams, the cesium decontamination factor (DF) will be measured for a non-radioactive, simulated, high-level waste solution. The test objectives, process outlines, and broad characterization of the waste streams are described.

  11. Development and properties of crystalline silicotitanate (CST) ion exchangers for radioactive waste applications

    SciTech Connect

    Miller, J.E.; Brown, N.E.

    1997-04-01

    Crystalline silicotitanates (CSTs) are a new class of ion exchangers that were jointly invented by researchers at Sandia National Laboratories and Texas A&M University. One particular CST, known as TAM-5, is remarkable for its ability to separate parts-per-million concentrations of cesium from highly alkaline solutions (pH> 14) containing high sodium concentrations (>5M). It is also highly effective for removing cesium from neutral and acidic solutions, and for removing strontium from basic and neutral solutions. Cesium isotopes are fission products that account for a large portion of the radioactivity in waste streams generated during weapons material production. Tests performed at numerous locations with early lab-scale TAM-5 samples established the material as a leading candidate for treating radioactive waste volumes such as those found at the Hanford site in Washington. Thus Sandia developed a Cooperative Research and Development Agreement (CRADA) partnership with UOP, a world leader in developing, commercializing, and supplying adsorbents and associated process technology to commercialize and further develop the material. CSTs are now commercially available from UOP in a powder (UOP IONSIV{reg_sign} IE-910 ion exchanger) and granular form suitable for column ion exchange operations (UOP IONSIV{reg_sign} IE-911 ion exchanger). These materials exhibit a high capacity for cesium in a wide variety of solutions of interest to the Department of Energy, and they are chemically, thermally, and radiation stable. They have performed well in tests at numerous sites with actual radioactive waste solutions, and are being demonstrated in the 100,000 liter Cesium Removal Demonstration taking place at Oak Ridge National Laboratory with Melton Valley Storage Tank waste. It has been estimated that applying CSTs to the Hanford cleanup alone will result in a savings of more than $300 million over baseline technologies.

  12. Synthesis and Characterization of Templated Ion Exchange Resins for the Selective Complexation of Actinide Ions

    SciTech Connect

    Uy, O. Manual

    2001-03-01

    The purpose of this research is to develop a polymeric extractant for the selective complexation of uranyl ions (and subsequently other actinyl and actinide ions) from aqueous solutions (lakes, streams, waste tanks and even body fluids). Chemical insights into what makes a good complexation site will be used to synthesize reagents tailor-made for the complexation of uranyl and other actinide ions. These insights, derived from studies of molecular recognition include ion coordination number and geometry, ionic size and ionic shape, as well as ion to ligand thermodynamic affinity. Selectivity for a specific actinide ion will be obtained by providing the polymers with cavities lined with complexing ligands so arranged as to match the charge, coordination number, coordination geometry, and size of the actinide metal ion. These cavity-containing polymers will be produced by using a specific ion (or surrogate) as a template around which monomeric complexing ligands will be polymerized. The complexing ligands will be ones containing functional groups known to form stable complexes with a specific ion and less stable complexes with other cations. Prior investigator's approaches for making templated resins for metal ions have had marginal success. We have extended and amended these methodologies in our work with Pb(II) and uranyl ion, by changing the order of the steps, by the inclusion of sonication, by using higher complex loading, and the selection of functional groups with better complexation constants. This has resulted in significant improvements to selectivity. The unusual shape of the uranyl ion suggests that this approach will result in even greater selectivities than already observed for Pb(II). Preliminary data obtained for uranyl templated polymers shows unprecedented selectivity and has resulted in the first ion selective electrode for uranyl ion.

  13. Nuclear quantum effects in water exchange around lithium and fluoride ions

    SciTech Connect

    Wilkins, David M.; Manolopoulos, David; Dang, Liem X.

    2015-02-14

    We employ classical and ring polymer molecular dynamics simulations to study the effect of nuclear quantum fluctuations on the structure and the water exchange dynamics of aqueous solutions of lithium and fluoride ions. While we obtain reasonably good agreement with experimental data for solutions of lithium by augmenting the Coulombic interactions between the ion and the water molecules with a standard Lennard-Jones ion-oxygen potential, the same is not true for solutions of fluoride, for which we find that a potential with a softer repulsive wall gives much better agreement. A small degree of destabilization of the first hydration shell is found in quantum simulations of both ions when compared with classical simulations, with the shell becoming less sharply defined and the mean residence time of the water molecules in the shell decreasing. In line with these modest differences, we find that the mechanisms of the water exchange reactions are unaffected by quantization, so a classical description of these reactions gives qualitatively correct and quantitatively reasonable results. We also find that the quantum effects in solutions of lithium are larger than in solutions of fluoride. This is partly due to the stronger interaction of lithium with water molecules, partly due to the lighter mass of lithium, and partly due to competing quantum effects in the hydration of fluoride, which are absent in the hydration of lithium. LXD was supported by US Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences.

  14. On the influence of ion exchange on the local structure of the titanosilicate ETS-10.

    PubMed

    Pavel, Claudiu C; Zibrowius, Bodo; Löffler, Elke; Schmidt, Wolfgang

    2007-07-14

    The effect of ion exchange with different monovalent cations (NH(4)(+), K(+), Na(+) and Cs(+)) on the local structure of the titanosilicate ETS-10 has been studied by (29)Si MAS NMR and Raman spectroscopy. Although X-ray diffraction shows no significant influence of ion exchange on the long range order, ammonium exchange is found to result in substantial damage to the local structure. Ion exchange experiments with alkali cations under significantly more acidic conditions clearly show that the structural damage brought about by ammonium exchange is not caused by the low pH of the exchange solution. The exchange with potassium and caesium ions also leads to significant changes in the (29)Si NMR and Raman spectra. However, these changes can largely be reversed by sodium back-exchange.

  15. Glucans monomer-exchange dynamics as an open chemical network

    SciTech Connect

    Rao, Riccardo Esposito, Massimiliano; Lacoste, David

    2015-12-28

    We describe the oligosaccharides-exchange dynamics performed by the so-called D-enzymes on polysaccharides. To mimic physiological conditions, we treat this process as an open chemical network by assuming some of the polymer concentrations fixed (chemostatting). We show that three different long-time behaviors may ensue: equilibrium states, nonequilibrium steady states, and continuous growth states. We dynamically and thermodynamically characterize these states and emphasize the crucial role of conservation laws in identifying the chemostatting conditions inducing them.

  16. Chemical exchange in biomacromolecules: Past, present, and future

    NASA Astrophysics Data System (ADS)

    Palmer, Arthur G.

    2014-04-01

    The perspective reviews quantitative investigations of chemical exchange phenomena in proteins and other biological macromolecules using NMR spectroscopy, particularly relaxation dispersion methods. The emphasis is on techniques and applications that quantify the populations, interconversion kinetics, and structural features of sparsely populated conformational states in equilibrium with a highly populated ground state. Applications to folding, molecular recognition, catalysis, and allostery by proteins and nucleic acids are highlighted.

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

    DOEpatents

    McCandless, Frank P.; Herbst, Ronald S.

    1995-01-01

    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.

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

    DOEpatents

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

    1995-05-30

    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.

  19. Heuristic overlap-exchange model of noble gas chemical shifts

    NASA Astrophysics Data System (ADS)

    Adrian, Frank J.

    2004-05-01

    It is now generally recognized that overlap-exchange interactions are the primary cause of the medium-dependent magnetic shielding (chemical shift) in all noble gases except helium, although the attractive electrostatic-dispersion (van der Waals) interactions play an indirect role in determining the penetration of the interacting species into the repulsive overlap-exchange region. The short-range nature of these overlap-exchange interactions, combined with the fact that they often can be approximated by simple functions of the overlap of the wave functions of the interacting species, suggests a useful semiempirical model of these chemical shifts. In it the total shielding is the sum of shieldings due to pairwise interactions of the noble gas atom with the individual atoms of the medium, with the "atomic" shielding terms either estimated by simple functions of the atomic overlap integrals averaged over their Boltzmann-weighted separations, or determined by fits to experimental data in systems whose complexity makes the former procedure impractical. Results for 129Xe chemical shifts in the noble gases and in a variety of molecular and condensed systems, including families of n-alkanes, straight-chain alcohols, and the endohedral compounds Xe@C60 and Xe@C70 are encouraging for the applicability of the model to systems of technical and biomedical interest.

  20. Chromatographic separation of neodymium isotopes by using chemical exchange process.

    PubMed

    Ismail, I M; Ibrahim, M; Aly, H F; Nomura, M; Fujii, Y

    2011-05-20

    The neodymium isotope effects were investigated in Nd-malate ligand exchange system using the highly porous cation exchange resin SQS-6. The temperature of the chromatographic columns was kept constant at 50°C by temperature controlled water passed through the columns jackets. The separation coefficient of neodymium isotopes, ɛ's, was calculated from the isotopic ratios precisely measured by means of an ICP mass spectrometer equipped with nine collectors as ion detectors. The separation coefficient, ɛ×10(5), were calculated and found to be 1.4, 4.8, 5.4, 10.6, 16.8 and 20.2 for (143)Nd, (144)Nd, (145)Nd, (146)Nd, (148)Nd and (150)Nd, respectively.

  1. Rate theory of solvent exchange and kinetics of Li+ - BF4-/PF6- ion pairs in acetonitrile

    NASA Astrophysics Data System (ADS)

    Dang, Liem X.; Chang, Tsun-Mei

    2016-09-01

    In this paper, we describe our efforts to apply rate theories in studies of solvent exchange around Li+ and the kinetics of ion pairings in lithium-ion batteries (LIBs). We report one of the first computer simulations of the exchange dynamics around solvated Li+ in acetonitrile (ACN), which is a common solvent used in LIBs. We also provide details of the ion-pairing kinetics of Li+-[BF4] and Li+-[PF6] in ACN. Using our polarizable force-field models and employing classical rate theories of chemical reactions, we examine the ACN exchange process between the first and second solvation shells around Li+. We calculate exchange rates using transition state theory and weighted them with the transmission coefficients determined by the reactive flux, Impey, Madden, and McDonald approaches, and Grote-Hynes theory. We found the relaxation times changed from 180 ps to 4600 ps and from 30 ps to 280 ps for Li+-[BF4] and Li+-[PF6] ion pairs, respectively. These results confirm that the solvent response to the kinetics of ion pairing is significant. Our results also show that, in addition to affecting the free energy of solvation into ACN, the anion type also should significantly influence the kinetics of ion pairing. These results will increase our understanding of the thermodynamic and kinetic properties of LIB systems.

  2. Rate theory of solvent exchange and kinetics of Li(+) - BF4 (-)/PF6 (-) ion pairs in acetonitrile.

    PubMed

    Dang, Liem X; Chang, Tsun-Mei

    2016-09-07

    In this paper, we describe our efforts to apply rate theories in studies of solvent exchange around Li(+) and the kinetics of ion pairings in lithium-ion batteries (LIBs). We report one of the first computer simulations of the exchange dynamics around solvated Li(+) in acetonitrile (ACN), which is a common solvent used in LIBs. We also provide details of the ion-pairing kinetics of Li(+)-[BF4] and Li(+)-[PF6] in ACN. Using our polarizable force-field models and employing classical rate theories of chemical reactions, we examine the ACN exchange process between the first and second solvation shells around Li(+). We calculate exchange rates using transition state theory and weighted them with the transmission coefficients determined by the reactive flux, Impey, Madden, and McDonald approaches, and Grote-Hynes theory. We found the relaxation times changed from 180 ps to 4600 ps and from 30 ps to 280 ps for Li(+)-[BF4] and Li(+)-[PF6] ion pairs, respectively. These results confirm that the solvent response to the kinetics of ion pairing is significant. Our results also show that, in addition to affecting the free energy of solvation into ACN, the anion type also should significantly influence the kinetics of ion pairing. These results will increase our understanding of the thermodynamic and kinetic properties of LIB systems.

  3. Ion Exchange Column Tests Supporting Technetium Removal Resin Maturation

    SciTech Connect

    Nash, C.; McCabe, D.; Hamm, L.; Smith, F.; Morse, M.

    2013-12-20

    The primary treatment of the tank waste at the DOE Hanford site will be done in the Waste Treatment and Immobilization Plant, currently under construction. The baseline plan for this facility is to treat the waste, splitting it into High Level Waste (HLW) and Low Activity Waste (LAW). Both waste streams are then separately vitrified as glass and sealed in canisters. The LAW glass will be disposed on site. There are currently no plans to treat the waste to remove technetium, so its disposition path is the LAW glass. Due to the soluble properties of pertechnetate and long half-life of 99Tc, effective management of 99Tc is important. Options are being explored to immobilize the supplemental LAW portion of the tank waste, as well as to examine the volatility of 99Tc during the vitrification process. Removal of 99Tc, followed by off-site disposal has potential to reduce treatment and disposal costs. A conceptual flow sheets for supplemental LAW treatment and disposal that could benefit from technetium removal will specifically examine removing 99Tc from the LAW feed stream to supplemental immobilization. SuperLig® 639 is an elutable ion exchange resin. In the tank waste, 99Tc is predominantly found in the tank supernate as pertechnetate (TcO4-). Perrhenate (ReO4-) has been shown to be a good non-radioactive surrogate for pertechnetate in laboratory testing for this ion exchange resin. This report contains results of experimental ion exchange distribution coefficient and column resin maturation kinetics testing using the resin SuperLig® 639a to selectively remove perrhenate from simulated LAW. This revision includes results from testing to determine effective resin operating temperature range. Loading tests were performed at 45°C, and the computer modeling was updated to include the temperature effects. Equilibrium contact testing indicated that this batch of

  4. Ion Exchange Testing with SRF Resin FY 2012

    SciTech Connect

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

    2014-07-02

    Ion exchange using spherical resorcinol-formaldehyde (SRF) resin has been selected by the U.S. Department of Energy’s Office of River Protection (DOE-ORP) for use in the Pretreatment Facility (PTF) of the Hanford Tank Waste Treatment and Immobilization Plant (WTP) and for potential application in at-tank deployment. Numerous studies have shown SRF resin to be effective for removing 137Cs from a wide variety of actual and simulated tank waste supernatants (Adamson et al. 2006; Blanchard et al. 2008; Burgeson et al. 2004; Duignan and Nash 2009; Fiskum et al. 2006a; Fiskum et al. 2006b; Fiskum et al. 2006c; Fiskum et al. 2007; Hassan and Adu-Wusu 2003; King et al. 2004; Nash et al. 2006). Prior work at the Pacific Northwest National Laboratory (PNNL) has focused primarily on the loading behavior for 4 to 6 M Na solutions at 25 to 45°C. Recent proposed changes to the WTP ion exchange process baseline indicate that loading may include a broader range of sodium molarities (0.1 to 8 M) and higher temperatures (50°C) to alleviate post-filtration precipitation issues. This report discusses ion exchange loading kinetics testing activities performed in accordance with Test Plan TP-WTPSP-002, Rev. 3.01, which was prepared and approved in response to the Test Specification 24590-PTF-TSP-RT-09-002, Rev. 0 (Lehrman 2010) and Test Exception 24590-PTF-TEF-RT-11-00003, Rev. 0 (Meehan 2011). This testing focused on column tests evaluating the impact of elevated temperature on resin degradation over an extended period of time and batch contacts evaluating the impact on Cs loading over a broad range of sodium concentrations (0.1 to 5 M). These changes may be required to alleviate post-filtration precipitation issues and broaden the data range of SRF resin loading under the conditions expected with the new equipment and process changes.

  5. Small Column Ion Exchange Design and Safety Strategy

    SciTech Connect

    Huff, T.; Rios-Armstrong, M.; Edwards, R.; Herman, D.

    2011-02-07

    Small Column Ion Exchange (SCIX) is a transformational technology originally developed by the Department of Energy (DOE) Environmental Management (EM-30) office and is now being deployed at the Savannah River Site (SRS) to significantly increase overall salt processing capacity and accelerate the Liquid Waste System life-cycle. The process combines strontium and actinide removal using Monosodium Titanate (MST), Rotary Microfiltration, and cesium removal using Crystalline Silicotitanate (CST, specifically UOP IONSIV{reg_sign}IE-911 ion exchanger) to create a low level waste stream to be disposed in grout and a high level waste stream to be vitrified. The process also includes preparation of the streams for disposal, e.g., grinding of the loaded CST material. These waste processing components are technically mature and flowsheet integration studies are being performed including glass formulations studies, application specific thermal modeling, and mixing studies. The deployment program includes design and fabrication of the Rotary Microfilter (RMF) assembly, ion-exchange columns (IXCs), and grinder module, utilizing an integrated system safety design approach. The design concept is to install the process inside an existing waste tank, Tank 41H. The process consists of a feed pump with a set of four RMFs, two IXCs, a media grinder, three Submersible Mixer Pumps (SMPs), and all supporting infrastructure including media receipt and preparation facilities. The design addresses MST mixing to achieve the required strontium and actinide removal and to prevent future retrieval problems. CST achieves very high cesium loadings (up to 1,100 curies per gallon (Ci/gal) bed volume). The design addresses the hazards associated with this material including heat management (in column and in-tank), as detailed in the thermal modeling. The CST must be size reduced for compatibility with downstream processes. The design addresses material transport into and out of the grinder and

  6. Cesium Ion Exchange Loading Kinetics Testing with SRF Resin

    SciTech Connect

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

    2012-11-02

    Ion exchange using the Spherical Resorcinol-Formaldehyde (SRF) resin has been selected by the U.S. Department of Energy’s Office of River Protection for use in the Pretreatment Facility of the Hanford Tank Waste Treatment and Immobilization Plant (WTP) and for potential application in an at-tank deployment for removing 137Cs. Recent proposed changes to the WTP ion exchange process baseline indicate that loading may include a broader range of sodium molarities (2 to 8 M) due to caustic leaching and higher temperatures (50°C) to alleviate post-filtration precipitation issues prior to reaching the ion exchange columns. Therefore, it is important to understand the behavior of SRF resin performance under the conditions expected with the new equipment and process changes. This research examined the impact of linear load velocity (4, 6, 8 cm/min), initial sodium concentration (2, 5, 8 M), initial sodium-to-cesium ratio (1.4E+05, 2.1E+05, 2.8E+05 mol/mol), initial sodium-to-hydroxide ratio (2.0, 3.0, 4.0 mol/mol), and resin degradation during extended solution flow using elevated temperature (45°, 50°, 55°, 60°, 65°, 75°C). Testing was performed using a~2mL column packed with SRF resin with feed flowing through it in an up-flow pattern. Samples were taken at set intervals and the data analyzed to help understand the impact of these conditions on the SRF resin performance. It was found that the loading kinetics were not significantly impacted by the sodium concentration over the range tested. However, the loading kinetics were impacted by the linear load velocity. These results indicated that at the test temperature, the adsorption of cesium is strongly dependent on mass transfer through the film and not significantly impacted by interparticle diffusion. Testing for extended times at elevated temperatures showed that the resin does degrade and loading capacity is reduced at and above 45°C. Above 60°C the resin appears to not load at all.

  7. Development and Evaluation of Oral Controlled Release Chlorpheniramine-Ion Exchange Resinate Suspension

    PubMed Central

    Kadam, A. U.; Sakarkar, D. M.; Kawtikwar, P. S.

    2008-01-01

    An oral controlled release suspension of chlorpheniramine maleate was prepared using ion-exchange resin technology. A strong cation exchange resin Indion 244 was utilized for the sorption of the drug and the drug resinates was evaluated for various physical and chemical parameters. The drug-resinate complex was microencapsulated with a polymer Eudragit RS 100 to further retard the release characteristics. Both the drug-resinate complex and microencapsulated drug resinate were suspended in a palatable aqueous suspension base and were evaluated for controlled release characteristic. Stability study indicated that elevated temperature did not alter the sustained release nature of the dosage form indicating that polymer membrane surrounding the core material remained intact throughout the storage period. PMID:20046790

  8. Ion Exchange Technology Development in Support of the Urine Processor Assembly

    NASA Technical Reports Server (NTRS)

    Mitchell, Julie; Broyan, James; Pickering, Karen

    2013-01-01

    The urine processor assembly (UPA) on the International Space Station (ISS) recovers water from urine via a vacuum distillation process. The distillation occurs in a rotating distillation assembly (DA) where the urine is heated and subjected to sub-ambient pressure. As water is removed, the original organics, salts, and minerals in the urine become more concentrated and result in urine brine. Eventually, water removal will concentrate the urine brine to super saturation of individual constituents, and precipitation occurs. Under typical UPA DA operating conditions, calcium sulfate or gypsum is the first chemical to precipitate in substantial quantity. During preflight testing with ground urine, the UPA achieved 85% water recovery without precipitation. However, on ISS, it is possible that crewmember urine can be significantly more concentrated relative to urine from ground donors. As a result, gypsum precipitated in the DA when operating at water recovery rates at or near 85%, causing the failure and subsequent re14 NASA Tech Briefs, September 2013 placement of the DA. Later investigations have demonstrated that an excess of calcium and sulfate will cause precipitation at water recovery rates greater than 70%. The source of the excess calcium is likely physiological in nature, via crewmembers' bone loss, while the excess sulfate is primarily due to the sulfuric acid component of the urine pretreatment. To prevent gypsum precipitation in the UPA, the Precipitation Prevention Project (PPP) team has focused on removing the calcium ion from pretreated urine, using ion exchange resins as calcium removal agents. The selectivity and effectiveness of ion exchange resins are determined by such factors as the mobility of the liquid phase through the polymer matrix, the density of functional groups, type of functional groups bound to the matrix, and the chemical characteristics of the liquid phase (pH, oxidation potential, and ionic strength). Previous experience with ion

  9. Determination of effective capacities of ion-exchangeable materials by measuring the equilibrium conductivity.

    PubMed

    Okabe, Toshiaki; Yokoyama, Yukio

    2010-01-01

    The effective ion-exchange capacities of ion-exchange materials were determined by measuring the change in the equilibrium conductivity of a column packed with analyte. The developed instrumental method can provide effective ion-exchange capacities for both cation and anion exchangers with simple operations. The cation-exchange capacity of a weak-acid cation-exchange resin (TSKgel SuperIC-Cation column) depended on the conditioning pH and the molar concentration of the conditioning agent. Plots of effective cation-exchange capacities over the conditioning pH exhibited three inflection points, suggesting the presence of two carboxy groups and one phenolic OH group in the resin, probably due to the inherent base polymer. This method was applied to several commercial analytical columns for ion chromatography, and could provide scientifically useful results for characterizing the resin properties.

  10. Electrodialysis-ion exchange for the separation of dissolved salts

    SciTech Connect

    Baroch, C.J.; Grant, P.J.

    1995-10-01

    The Department of Energy generates and stores a significant quantity of low level, high level, and mixed wastes. As some of the DOE facilities are decontaminated and decommissioned, additional and possibly different forms of wastes will be generated. A significant portion of these wastes are aqueous streams containing acids, bases, and salts, or are wet solids containing inorganic salts. Some of these wastes are quite dilute solutions, whereas others contain large quantities of nitrates either in the form of dissolved salts or acids. Many of the wastes are also contaminated with heavy metals, radioactive products, or organics. Some of these wastes are in storage because a satisfactory treatment and disposal processes have not been developed. There is considerable interest in developing processes that remove or destroy the nitrate wastes. Electrodialysis-Ion Exchange (EDIX) is a possible process that should be more cost effective in treating aqueous waste steams. This report describes the EDIX process.

  11. Recovery of very dilute acetic acid using ion exchange

    SciTech Connect

    Cloete, F.L.D.; Marais, A.P.

    1995-07-01

    Acetic and related acids occur in many industrial wastewaters, often mixed with several other classes of organic compounds. Acetic acid can be recovered from 1% solutions using weakly basic ion exchange resins. The acid is adsorbed by the free-base form of the resin, which can then be eluted using a slurry of lime to give a solution of calcium acetate. This solution could either be evaporated to crystallize calcium acetate or reacted with sulfuric acid to form acetic acid and gypsum. Laboratory tests of the proposed process gave product solutions of 15--20% acetic acid using pure 1% acetic acid as feed. Some measurements using a typical industrial effluent gave similar recoveries and showed that there was no initial fouling of the resins.

  12. Advanced integrated solvent extraction and ion exchange systems

    SciTech Connect

    Horwitz, P.

    1996-10-01

    Advanced integrated solvent extraction (SX) and ion exchange (IX) systems are a series of novel SX and IX processes that extract and recover uranium and transuranics (TRUs) (neptunium, plutonium, americium) and fission products {sup 90}Sr, {sup 99}Tc, and {sup 137}Cs from acidic high-level liquid waste and that sorb and recover {sup 90}Sr, {sup 99}Tc, and {sup 137}Cs from alkaline supernatant high-level waste. Each system is based on the use of new selective liquid extractants or chromatographic materials. The purpose of the integrated SX and IX processes is to minimize the quantity of waste that must be vitrified and buried in a deep geologic repository by producing raffinates (from SX) and effluent streams (from IX) that will meet the specifications of Class A low-level waste.

  13. Ion Exchange Resin Bead Decoupled High-Pressure Electroosmotic Pump

    PubMed Central

    Yang, Bingcheng; Zhang, Feifang; Liang, Xinmiao; Dasgupta, Purnendu K.; Liu, Shaorong

    2009-01-01

    We describe an electroosmotic pump (EOP) that utilizes a cation exchange resin bead as the electric field decoupler. The resin bead serves as a electrical grounding joint without fluid leakage, thus eliminating electrolytic gas interference from the flow channels. The arrangement is easy to practice from readily available components, displays a very low electrical resistance, and is capable of bearing high backpressure (at least 3200 psi). We use a silica xerogel column as the EOP element to pump water and demonstrate a complete capillary ion chromatograph (CIC), which uses a similar bead based microelectrodialytic generator (μ-EDG) to generate a KOH eluent from the pumped water. We observed good operational stability of the complete arrangement over long periods. PMID:19449862

  14. Chemical Shuttle Additives in Lithium Ion Batteries

    SciTech Connect

    Patterson, Mary

    2013-03-31

    than NMC) and the DDB is useful for lithium ion cells with LFP cathodes (potential that is lower than NMC). A 4.5 V class redox shuttle provided by Argonne National Laboratory was evaluated which provides a few cycles of overcharge protection for lithium ion cells containing NMC cathodes but it is not stable enough for consideration. Thus, a redox shuttle with an appropriate redox potential and sufficient chemical and electrochemical stability for commercial use in larger format lithium ion cells with NMC cathodes was not found. Molecular imprinting of the redox shuttle molecule during solid electrolyte interphase (SEI) layer formation likely contributes to the successful reduction of oxidized redox shuttle species at carbon anodes. This helps to understand how a carbon anode covered with an SEI layer, that is supposed to be electrically insulating, can reduce the oxidized form of a redox shuttle.

  15. Transverse relaxation in the rotating frame induced by chemical exchange

    NASA Astrophysics Data System (ADS)

    Michaeli, Shalom; Sorce, Dennis J.; Idiyatullin, Djaudat; Ugurbil, Kamil; Garwood, Michael

    2004-08-01

    In the presence of radiofrequency irradiation, relaxation of magnetization aligned with the effective magnetic field is characterized by the time constant T1 ρ. On the other hand, the time constant T2 ρ characterizes the relaxation of magnetization that is perpendicular to the effective field. Here, it is shown that T2 ρ can be measured directly with Carr-Purcell sequences composed of a train of adiabatic full-passage (AFP) pulses. During adiabatic rotation, T2 ρ characterizes the relaxation of the magnetization, which under adiabatic conditions remains approximately perpendicular to the time-dependent effective field. Theory is derived to describe the influence of chemical exchange on T2 ρ relaxation in the fast-exchange regime, with time constant defined as T2 ρ,ex . The derived theory predicts the rate constant R 2ρ, ex (=1/T 2ρ, ex) to be dependent on the choice of amplitude- and frequency-modulation functions used in the AFP pulses. Measurements of R2 ρ,ex of the water/ethanol exchanging system confirm the predicted dependence on modulation functions. The described theoretical framework and adiabatic methods represent new tools to probe exchanging systems.

  16. Exchange bias in polycrystalline magnetite films made by ion-beam assisted deposition

    SciTech Connect

    Kaur, Maninder; Qiang, You; Jiang, Weilin; Burks, Edward C.; Liu, Kai; Namavar, Fereydoon; McCloy, John S.

    2014-11-07

    Iron oxide films were produced using ion-beam-assisted deposition, and Raman spectroscopy and x-ray diffraction indicate single-phase magnetite. However, incorporation of significant fractions of argon in the films from ion bombardment is evident from chemical analysis, and Fe/O ratios are lower than expected from pure magnetite, suggesting greater than normal disorder. Low temperature magnetometry and first-order reversal curve measurements show strong exchange bias, which likely arises from defects at grain boundaries, possibly amorphous, creating frustrated spins. Since these samples contain grains ∼6 nm, a large fraction of the material consists of grain boundaries, where spins are highly disordered and reverse independently with external field.

  17. Peptide Orientation Affects Selectivity in Ion-Exchange Chromatography

    SciTech Connect

    Alpert, Andrew J.; Petritis, Konstantinos; Kangas, Lars J.; Smith, R. D.; Mechtler, Karl; Mitulovic, Goran; Mohammed, Shabaz; Heck, Albert J.

    2010-06-15

    Here we demonstrate that separation of proteolytic peptides, having the same net charge and one basic residue, is affected by their specific orientation toward the stationary phase in ion-exchange chromatography. In electrostatic repulsion-hydrophilic interaction chromatography (ERLIC) with an anion-exchange material, the C-terminus of the peptides is, on average, oriented toward the stationary phase. In cation exchange, the average peptide orientation is the opposite. Data with synthetic peptides, serving as orientation probes, indicate that in tryptic/ Lys-C peptides the C-terminal carboxyl group appears to be in a zwitterionic bond with the side chain of the C-terminal Lys/Arg residue. In effect, the side chain is then less basic than the N-terminus, accounting for the specific orientation of tryptic and Lys-C peptides. Analyses of larger sets of peptides, generated from lysates by either Lys-N, Lys-C, or trypsin, reveal that specific peptide orientation affects the ability of charged side chains, such as phosphate residues, to influence retention. Phosphorylated residues that are remote in the sequence from the binding site affect retention less than those that are closer. When a peptide contains multiple charged sites, then orientation is observed to be less rigid and retention tends to be governed by the peptide’s net charge rather than its sequence. These general observations could be of value in confirming a peptide’s identification and, in particular, phosphosite assignments in proteomics analyses. More generally, orientation accounts for the ability of chromatography to separate peptides of the same composition but different sequence.

  18. Peptide Orientation Affects Selectivity in Ion-Exchange Chromatography

    SciTech Connect

    Alpert, Andrew J.; Petritis, Konstantinos; Kangas, Lars J.; Smith, Richard D.; Mechtler, Karl; Mitulovic, Goran; Mohammed, Shabaz; Heck, Albert J.

    2010-06-15

    Here we demonstrate that separation of proteolytic peptides, having the same net charge and one basic residue, is affected by their specific orientation toward the stationary phase in ion-exchange chromatography. In electrostatic repulsion-hydrophilic interaction chromatography (ERLIC) with an anion-exchange material, the C-terminus of the peptides is, on average, oriented toward the stationary phase. In cation exchange, the average peptide orientation is the opposite. Data with synthetic peptides, serving as orientation probes, indicate that in tryptic/Lys-C peptides the C-terminal carboxyl group appears to be in a zwitterionic bond with the side chain of the C-terminal Lys/Arg residue. In effect, the side chain is then less basic than the N-terminus, accounting for the specific orientation of tryptic and Lys-C peptides. Analyses of larger sets of peptides, generated from lysates by either Lys-N, Lys-C, or trypsin, reveal that specific peptide orientation affects the ability of harged side chains, such as phosphate residues, to influence retention. Phosphorylated residues that are remote in the sequence from the binding site affect retention less than those that are closer. When a peptide contains multiple charged sites, then orientation is observed to be less rigid and retention tends to be governed by the peptide’s net charge rather than its sequence. These general observations could be of value in confirming a peptide’s identification and, in particular, phosphosite assignments in proteomics analyses. More generally, orientation accounts for the ability of chromatography to separate peptides of the same compositionbut different sequence.

  19. Understanding the Rates and Molecular Mechanism of Water-Exchange around Aqueous Ions Using Molecular Simulations

    SciTech Connect

    Annapureddy, Harsha V.; Dang, Liem X.

    2014-07-31

    Solvation processes occurring around aqueous ions are of fundamental importance in physics, chemistry, and biology. Over the past few decades, several experimental and theoretical studies were devoted to understanding ion solvation and the processes involved in it. In this article, we present a summary of our recent efforts that, through computer simulations, focused on providing a comprehensive understanding of solvent-exchange processes around aqueous ions. To accomplish these activities, we have looked at the mechanistic properties associated with the water-exchange process, such as potentials of mean force, time-dependent transmission coefficients, and the corresponding rate constants using transition rate theory, the reactive flux method, and Grote-Hynes treatments of the dynamic response of the solvent. The Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences (BES), of the U.S. Department of Energy (DOE) funded this work. Battelle operates Pacific Northwest National Laboratory for DOE. The calculations were carried out using computer resources provided by BES.

  20. In vivo multicolor molecular MR imaging using diamagnetic chemical exchange saturation transfer liposomes.

    PubMed

    Liu, Guanshu; Moake, Matthew; Har-el, Yah-el; Long, Chris M; Chan, Kannie W Y; Cardona, Amanda; Jamil, Muksit; Walczak, Piotr; Gilad, Assaf A; Sgouros, George; van Zijl, Peter C M; Bulte, Jeff W M; McMahon, Michael T

    2012-04-01

    A variety of (super)paramagnetic contrast agents are available for enhanced MR visualization of specific tissues, cells, or molecules. To develop alternative contrast agents without the presence of metal ions, liposomes were developed containing simple bioorganic and biodegradable compounds that produce diamagnetic chemical exchange saturation transfer MR contrast. This diamagnetic chemical exchange saturation transfer contrast is frequency-dependent, allowing the unique generation of "multicolor" images. The contrast can be turned on and off at will, and standard images do not show the presence of these agents. As an example, glycogen, L-arginine, and poly-L-lysine were encapsulated inside liposomes and injected intradermally into mice to image the lymphatic uptake of these liposomes. Using a frequency-dependent acquisition scheme, it is demonstrated that multicolor MRI can differentiate between different contrast particles in vivo following their homing to draining lymph nodes. Being nonmetallic and bioorganic, these diamagnetic chemical exchange saturation transfer liposomes form an attractive novel platform for multicolor imaging in vivo.

  1. Modeling of Crystalline Silicotitanate Ion Exchange Columns Using Experimental Data from SRS Simulated Waste

    SciTech Connect

    Walker, D.D.

    1999-03-15

    Non-elutable ion exchange using crystalline silicotitanate is being considered for removing cesium from Savannah River Site radioactive waste. The construction cost of this process depends strongly on the size of the ion exchange column required to meet product specifications.

  2. Truly incomplete and complex exchanges in prematurely condensed chromosomes of human fibroblasts exposed in vitro to energetic heavy ions

    NASA Technical Reports Server (NTRS)

    Wu, Honglu; Durante, Marco; Furusawa, Yoshiya; George, Kerry; Kawata, Tetsuya; Cucinotta, Francis A.

    2003-01-01

    Confluent human fibroblast cells (AG1522) were irradiated with gamma rays, 490 MeV/nucleon silicon ions, or iron ions at either 200 or 500 MeV/nucleon. The cells were allowed to repair at 37 degrees C for 24 h after exposure, and a chemically induced premature chromosome condensation (PCC) technique was used to condense chromosomes in the G2 phase of the cell cycle. Incomplete and complex exchanges were analyzed in the irradiated samples. To verify that chromosomal breaks were truly unrejoined, chromosome aberrations were analyzed using a combination of whole-chromosome specific probes and probes specific for the telomere region of the chromosome. Results showed that the frequency of unrejoined chromosome breaks was higher after irradiation with the heavy ions of high LET, and consequently the ratio of incomplete to complete exchanges increased steadily with LET up to 440 keV/microm, the highest LET included in the present study. For samples exposed to 200 MeV/nucleon iron ions, chromosome aberrations were analyzed using the multicolor FISH (mFISH) technique, which allows identification of both complex and truly incomplete exchanges. Results of the mFISH study showed that 0.7 and 3 Gy iron ions produced similar ratios of complex to simple exchanges and incomplete to complete exchanges; these ratios were higher than those obtained after exposure to 6 Gy gamma rays. After 0.7 Gy of iron ions, most complex aberrations were found to involve three or four chromosomes, which is a likely indication of the maximum number of chromosome domains traversed by a single iron-ion track.

  3. Cesium removal from liquid acidic wastes with the primary focus on ammonium molybdophosphate as an ion exchanger: A literature review

    SciTech Connect

    Miller, C.J.

    1995-03-01

    Many articles have been written concerning the selective removal of cesium from both acidic and alkaline defense wastes. The majority of the work performed for cesium removal from defense wastes involves alkaline feed solutions. Several different techniques for cesium removal from acidic solutions have been evaluated such as precipitation, solvent extraction, and ion exchange. The purpose of this paper is to briefly review various techniques for cesium removal from acidic solutions. The main focus of the review will be on ion exchange techniques, particularly those involving ammonium molybdophosphate as the exchanger. The pertinent literature sources are condensed into a single document for quick reference. The information contained in this document was used as an aid in determining techniques to evaluate cesium removal from the acidic Idaho Chemical Processing Plant waste matrices. 47 refs., 2 tabs.

  4. One- and two-dimensional chemical exchange nuclear magnetic resonance studies of the creatine kinase catalyzed reaction

    SciTech Connect

    Gober, J.R.

    1988-01-01

    The equilibrium chemical exchange dynamics of the creatine kinase enzyme system were studied by one- and two-dimensional {sup 31}P NMR techniques. Pseudo-first-order reaction rate constants were measured by the saturation transfer method under an array of experimental conditions of pH and temperature. Quantitative one-dimensional spectra were collected under the same conditions in order to calculate the forward and reverse reaction rates, the K{sub eq}, the hydrogen ion stoichiometry, and the standard thermodynamic functions. The pure absorption mode in four quadrant two-dimensional chemical exchange experiment was employed so that the complete kinetic matrix showing all of the chemical exchange process could be realized.

  5. Impact of sediment-seawater cation exchange on Himalayan chemical weathering fluxes

    NASA Astrophysics Data System (ADS)

    Lupker, Maarten; France-Lanord, Christian; Lartiges, Bruno

    2016-08-01

    Continental-scale chemical weathering budgets are commonly assessed based on the flux of dissolved elements carried by large rivers to the oceans. However, the interaction between sediments and seawater in estuaries can lead to additional cation exchange fluxes that have been very poorly constrained so far. We constrained the magnitude of cation exchange fluxes from the Ganga-Brahmaputra river system based on cation exchange capacity (CEC) measurements of riverine sediments. CEC values of sediments are variable throughout the river water column as a result of hydrological sorting of minerals with depth that control grain sizes and surface area. The average CEC of the integrated sediment load of the Ganga-Brahmaputra is estimated ca. 6.5 meq 100 g-1. The cationic charge of sediments in the river is dominated by bivalent ions Ca2+ (76 %) and Mg2+ (16 %) followed by monovalent K+ (6 %) and Na+ (2 %), and the relative proportion of these ions is constant among all samples and both rivers. Assuming a total exchange of exchangeable Ca2+ for marine Na+ yields a maximal additional Ca2+ flux of 28 × 109 mol yr-1 of calcium to the ocean, which represents an increase of ca. 6 % of the actual river dissolved Ca2+ flux. In the more likely event that only a fraction of the adsorbed riverine Ca2+ is exchanged, not only for marine Na+ but also Mg2+ and K+, estuarine cation exchange for the Ganga-Brahmaputra is responsible for an additional Ca2+ flux of 23 × 109 mol yr-1, while ca. 27 × 109 mol yr-1 of Na+, 8 × 109 mol yr-1 of Mg2+ and 4 × 109 mol yr-1 of K+ are re-absorbed in the estuaries. This represents an additional riverine Ca2+ flux to the ocean of 5 % compared to the measured dissolved flux. About 15 % of the dissolved Na+ flux, 8 % of the dissolved K+ flux and 4 % of the Mg2+ are reabsorbed by the sediments in the estuaries. The impact of estuarine sediment-seawater cation exchange appears to be limited when evaluated in the context of the long-term carbon cycle and

  6. Ion-exchange selectivities of periderm and cuticular membranes toward alkali cations

    SciTech Connect

    Ersoz, M.; Duncan, H.J.

    1994-08-01

    The ion-exchange selectivities of lithium, sodium, potassium, and cesium on isolated potato periderm (Solanum tuberosum) and pear fruit cuticular membranes were investigated; the general order of preference both for cation selectivities and ion-exchange capacities was lithium > sodium > potassium > cesium. The potato periderm and pear fruit cuticular membranes exhibited a behavior typical of ion-exchange resins of the weak acid type. At constant pH 7, the ion-exchange capacities of periderm and cuticular membranes increased with hydrated ionic radius, and also with increasing pH and neutral salt concentration, and decreased with crystal ionic radius. Counterion selectivities also exhibited the same behavior. The ion-exchange properties are discussed in terms of the structure and function of potato periderm and pear fruit cuticular membranes.

  7. Selective preconcentration of uranyl ion by silica gel phases modified with chelating compounds as inorganic polymeric ion exchangers.

    PubMed

    Mahmoud, Mohamed E; Kenawy, Ibrahim M M; Soliman, Ezzat M; Hafez, Medhat A; Akl, Magda A A; Lashein, Rabab R A

    2008-03-01

    Four chemically modified chelating silica gel phases (I - IV) with ion exchange groups were tested for their potential capability to selectively bind, extract and preconcentrate uranyl ions (UO(2)(2+)) from different aqueous solutions as well as ore samples. Factors affecting such determination processes were studied and optimized. These included the pH of the contact solution, the mass of the silica gel phase extractant, the stirring time during the application of a static technique and the eluent concentration for desorption of the surface-bound uranyl ion and interfering anions and cations. All these factors were evaluated on the basis of determinations of the distribution coefficient value (K(d)) and the percent recovery (R%). Percent recovery values of 91% for silica phase (II) and 93% for silica phase (IV) were identified in the optimum conditions. The proposed preconcentration method was further applied to uranium ore samples as well as granite samples. The determined percentage and ppm values are in good agreement with the standard assigned ones. The structure of the synthesized silica gel phases (I - IV) and their uranyl bound complexes were identified and characterized by means of infrared analysis, thermal analysis (TGA) and potentiometric titration.

  8. Ion Mobility Spectrometry-Hydrogen Deuterium Exchange Mass Spectrometry of Anions: Part 1. Peptides to Proteins

    NASA Astrophysics Data System (ADS)

    Donohoe, Gregory C.; Khakinejad, Mahdiar; Valentine, Stephen J.

    2015-04-01

    Ion mobility spectrometry (IMS) coupled with hydrogen deuterium exchange (HDX)-mass spectrometry (MS) has been used to study the conformations of negatively-charged peptide and protein ions. Results are presented for ion conformers of angiotensin 1, a synthetic peptide (SP), bovine insulin, ubiquitin, and equine cytochrome c. In general, the SP ion conformers demonstrate a greater level of HDX efficiency as a greater proportion of the sites undergo HDX. Additionally, these ions exhibit the fastest rates of exchange. Comparatively, the angiotensin 1 ions exhibit a lower rate of exchange and HDX level presumably because of decreased accessibility of exchange sites by charge sites. The latter are likely confined to the peptide termini. Insulin ions show dramatically reduced HDX levels and exchange rates, which can be attributed to decreased conformational flexibility resulting from the disulfide bonds. For the larger ubiquitin and protein ions, increased HDX is observed for larger ions of higher charge state. For ubiquitin, a conformational transition from compact to more elongated species (from lower to higher charge states) is reflected by an increase in HDX levels. These results can be explained by a combination of interior site protection by compact conformers as well as decreased access by charge sites. The elongated cytochrome c ions provide the largest HDX levels where higher values correlate with charge state. These results are consistent with increased exchange site accessibility by additional charge sites. The data from these enhanced IMS-HDX experiments are described in terms of charge site location, conformer rigidity, and interior site protection.

  9. Ion mobility spectrometry-hydrogen deuterium exchange mass spectrometry of anions: part 1. Peptides to proteins.

    PubMed

    Donohoe, Gregory C; Khakinejad, Mahdiar; Valentine, Stephen J

    2015-04-01

    Ion mobility spectrometry (IMS) coupled with hydrogen deuterium exchange (HDX)-mass spectrometry (MS) has been used to study the conformations of negatively-charged peptide and protein ions. Results are presented for ion conformers of angiotensin 1, a synthetic peptide (SP), bovine insulin, ubiquitin, and equine cytochrome c. In general, the SP ion conformers demonstrate a greater level of HDX efficiency as a greater proportion of the sites undergo HDX. Additionally, these ions exhibit the fastest rates of exchange. Comparatively, the angiotensin 1 ions exhibit a lower rate of exchange and HDX level presumably because of decreased accessibility of exchange sites by charge sites. The latter are likely confined to the peptide termini. Insulin ions show dramatically reduced HDX levels and exchange rates, which can be attributed to decreased conformational flexibility resulting from the disulfide bonds. For the larger ubiquitin and protein ions, increased HDX is observed for larger ions of higher charge state. For ubiquitin, a conformational transition from compact to more elongated species (from lower to higher charge states) is reflected by an increase in HDX levels. These results can be explained by a combination of interior site protection by compact conformers as well as decreased access by charge sites. The elongated cytochrome c ions provide the largest HDX levels where higher values correlate with charge state. These results are consistent with increased exchange site accessibility by additional charge sites. The data from these enhanced IMS-HDX experiments are described in terms of charge site location, conformer rigidity, and interior site protection.

  10. Gamma irradiation-induced modifications of polymers found in nuclear waste embedding processes Part II: The ion-exchange resin

    NASA Astrophysics Data System (ADS)

    Debré, O.; Nsouli, B.; Thomas, J.-P.; Stevenson, I.; Colombini, D.; Romero, M.-A.

    1997-08-01

    Ion exchange resins (IERs) saturated in cesium and borate ions are well representative of low and medium activity nuclear waste to be embedded in an epoxy resin/amine hardener, such a conditioning procedure being under qualification. In order to test these materials in realistic conditions they are externally irradiated (air and water), in mixed beds saturated in fixed ions (cesium and borate) and water. Irradiation effects are evidenced with the HSF-SIMS technique by the variation of the emission characteristic of both the fixed ions, the chemical structure of the IERs and their interrelationship, both from the analysis of the solid material and of the residual or rinsing water. It appears that the fixed ions can be released in surrounding water as a consequence of radiation-induced resin fragments solubility.

  11. Revised Thermal Analysis of LANL Ion Exchange Column

    SciTech Connect

    Laurinat, J

    2006-04-11

    This document updates a previous calculation of the temperature distributions in a Los Alamos National Laboratory (LANL) ion exchange column.1 LANL operates two laboratory-scale anion exchange columns, in series, to extract Pu-238 from nitric acid solutions. The Defense Nuclear Facilities Safety Board has requested an updated analysis to calculate maximum temperatures for higher resin loading capacities obtained with a new formulation of the Reillex HPQ anion exchange resin. The increased resin loading capacity will not exceed 118 g plutonium per L of resin bed. Calculations were requested for normal operation of the resin bed at the minimum allowable solution feed rate of 30 mL/min and after an interruption of flow at the end of the feed stage, when one of the columns is fully loaded. The object of the analysis is to demonstrate that the decay heat from the Pu-238 will not cause resin bed temperatures to increase to a level where the resin significantly degrades. At low temperatures, resin bed temperatures increase primarily due to decay heat. At {approx}70 C a Low Temperature Exotherm (LTE) resulting from the reaction between 8-12 M HNO{sub 3} and the resin has been observed. The LTE has been attributed to an irreversible oxidation of pendant ethyl benzene groups at the termini of the resin polymer chains by nitric acid. The ethyl benzene groups are converted to benzoic acid moities. The resin can be treated to permanently remove the LTE by heating a resin suspension in 8M HNO{sub 3} for 30-45 minutes. No degradation of the resin performance is observed after the LTE removal treatment. In fact, heating the resin in boiling ({approx}115-120 C) 12 M HNO{sub 3} for 3 hr displays thermal stability analogous to resin that has been treated to remove the LTE. The analysis is based on a previous study of the SRS Frames Waste Recovery (FWR) column, performed in support of the Pu-238 production campaign for NASA's Cassini mission. In that study, temperature transients

  12. The effect of electron beam irradiation on silver-sodium ion exchange in silicate glasses

    NASA Astrophysics Data System (ADS)

    Sidorov, Alexander I.; Prosnikov, Mikhail A.

    2016-04-01

    It is shown experimentally that electron irradiation of sodium-silicate glasses makes possible the control of the subsequent ion exchange Ag+ ↔ Na+ process in a salt melt. The reason of this effect is the negatively charged regions formation in a glass volume during electron irradiation. The electric field, produced by these regions in glass volume, results in positive Na+ ions field migration into them. The spatial redistribution of Na+ ions results in the decrease of the ion exchange efficiency, or the ion exchange can be even blocked. This led to the decrease of the luminescence intensity of neutral silver molecular clusters in the irradiated zone, and effect on the silver nanoparticles formation during the subsequent thermal treatment. The observed effects can be used for the control of ion exchange processes during integrated optics devices fabrication, and for the electron-beam recording of optical information.

  13. Chemical trend of exchange coupling in II-VI diluted magnetic semiconductors

    NASA Astrophysics Data System (ADS)

    Chanier, Thomas; Hayn, Roland; Virot, François

    2010-03-01

    We present an ab-initio study of the magnetic couplings in Mn- and Co-doped II-VI DMS ZnA (A=O,S,Se,Te). We show the necessity of taking into account the strong electron correlation on the transition metal (TM) 3d level to reproduce correctly the experimental chemical trend. Within the LSDA+U (local spin density approximation with a Hubbard-type correction to TM 3d electrons), we find (i) the d-d exchange couplings between nearest-neighbor magnetic ions to be antiferromagnetic (AFM) of the order of -1 meV and (ii) the sp-d exchange constants between magnetic ions and conduction (valence) band electrons (holes) Nα (Nβ) to be FM (AFM) of the order of 0.1 eV (-1 eV). In ZnMnO and ZnCoO, the strong p-d hybridisation leads to the presence of a bound state above the valence band, the failure of the commonly-used Larson perturbation theory formulae for p-d and d-d exchange interactions [1] and prevents high-Tc ferromagnetism [2]. [1] B. Larson et al. , PRB 37, 4137 (1988) [2] T. Chanier et al. , PRB 79, 205204 (2009)

  14. Lead Removal From Synthetic Leachate Matrices by a Novel Ion-Exchange Material

    NASA Technical Reports Server (NTRS)

    Street, Kenneth W., Jr.; Hovanitz, Edward S.; Chi, Sulan

    2002-01-01

    This report discusses the application of a novel polyacrylate-based ion-exchange material (IEM) for the removal of lead (Pb) ions from water. Preliminary testing includes the establishment of the operating pH range, capacity information, and the effect of calcium and anions in the matrix. Batch testing with powder indicates slightly different optimal operational conditions from those used for column testing. The ion exchanger is excellent for removing lead from aqueous solutions.

  15. Performance and cost characteristics of multi-electron transfer, common ion exchange non-aqueous redox flow batteries

    NASA Astrophysics Data System (ADS)

    Laramie, Sydney M.; Milshtein, Jarrod D.; Breault, Tanya M.; Brushett, Fikile R.; Thompson, Levi T.

    2016-09-01

    Non-aqueous redox flow batteries (NAqRFBs) have recently received considerable attention as promising high energy density, low cost grid-level energy storage technologies. Despite these attractive features, NAqRFBs are still at an early stage of development and innovative design techniques are necessary to improve performance and decrease costs. In this work, we investigate multi-electron transfer, common ion exchange NAqRFBs. Common ion systems decrease the supporting electrolyte requirement, which subsequently improves active material solubility and decreases electrolyte cost. Voltammetric and electrolytic techniques are used to study the electrochemical performance and chemical compatibility of model redox active materials, iron (II) tris(2,2‧-bipyridine) tetrafluoroborate (Fe(bpy)3(BF4)2) and ferrocenylmethyl dimethyl ethyl ammonium tetrafluoroborate (Fc1N112-BF4). These results help disentangle complex cycling behavior observed in flow cell experiments. Further, a simple techno-economic model demonstrates the cost benefits of employing common ion exchange NAqRFBs, afforded by decreasing the salt and solvent contributions to total chemical cost. This study highlights two new concepts, common ion exchange and multi-electron transfer, for NAqRFBs through a demonstration flow cell employing model active species. In addition, the compatibility analysis developed for asymmetric chemistries can apply to other promising species, including organics, metal coordination complexes (MCCs) and mixed MCC/organic systems, enabling the design of low cost NAqRFBs.

  16. Charge-exchange collisions of C 60z+ : a probe of the ion charge distribution

    NASA Astrophysics Data System (ADS)

    Cameron, Douglas B.; Parks, Joel H.

    1997-06-01

    We present Paul trap measurements of charge-exchange collisions of Li, Cs and C 60 with C 60z+ ions ( z = 1-3) at thermal energies. Surprisingly, the measured charge-exchange rates for each neutral species are not proportional to the ion charge z as would be expected for Langevin collisions involving a uniformly charged ion. The relative rates can be reproduced by a model based on a symmetric distribution of point charges that are free to move on the ion surface during the neutral trajectory. Such behavior can be attributed to static and possibly dynamic Jahn-Teller effects in C 60z+ ions.

  17. Protein-surface interaction maps for ion-exchange chromatography.

    PubMed

    Freed, Alexander S; Cramer, Steven M

    2011-04-05

    In this paper, protein-surface interaction maps were generated by performing coarse-grained protein-surface calculations. This approach allowed for the rapid determination of the protein-surface interaction energies at a range of orientations and distances. Interaction maps of lysozyme indicated that there was a contiguous series of orientations corresponding to several adjacent preferred binding regions on the protein surface. Examination of these orientations provided insight into the residues involved in surface interactions, which qualitatively agreed with the retention data for single-site mutants. Interaction maps of lysozyme single-site mutants were also generated and provided significant insight into why these variants exhibited significant differences in their chromatographic behavior. This approach was also employed to study the binding behavior of CspB and related mutants. The results indicated that, in addition to describing general trends in the data, these maps provided significant insight into retention data of the single-site mutants. In particular, subtle retention trends observed with the K12 and K13 mutants were well-described using this interaction map approach. Finally, the number of interaction points with energies stronger than -2 kcal/mol was shown to be able to semi-quantitatively predict the behavior of most of the mutants. This rapid approach for calculating protein-surface interaction maps is expected to facilitate future method development for separating closely related protein variants in ion-exchange systems.

  18. Ion-exchange chromatography for the characterization of biopharmaceuticals.

    PubMed

    Fekete, Szabolcs; Beck, Alain; Veuthey, Jean-Luc; Guillarme, Davy

    2015-09-10

    Ion-exchange chromatography (IEX) is a historical technique widely used for the detailed characterization of therapeutic proteins and can be considered as a reference and powerful technique for the qualitative and quantitative evaluation of charge heterogeneity. The goal of this review is to provide an overview of theoretical and practical aspects of modern IEX applied for the characterization of therapeutic proteins including monoclonal antibodies (Mabs) and antibody drug conjugates (ADCs). The section on method development describes how to select a suitable stationary phase chemistry and dimensions, the mobile phase conditions (pH, nature and concentration of salt), as well as the temperature and flow rate, considering proteins isoelectric point (pI). In addition, both salt-gradient and pH-gradient approaches were critically reviewed and benefits as well as limitations of these two strategies were provided. Finally, several applications, mostly from pharmaceutical industries, illustrate the potential of IEX for the characterization of charge variants of various types of biopharmaceutical products.

  19. Porous metal oxide microspheres from ion exchange resin

    NASA Astrophysics Data System (ADS)

    Picart, S.; Parant, P.; Caisso, M.; Remy, E.; Mokhtari, H.; Jobelin, I.; Bayle, J. P.; Martin, C. L.; Blanchart, P.; Ayral, A.; Delahaye, T.

    2015-07-01

    This study is devoted to the synthesis and the characterization of porous metal oxide microsphere from metal loaded ion exchange resin. Their application concerns the fabrication of uranium-americium oxide pellets using the powder-free process called Calcined Resin Microsphere Pelletization (CRMP). Those mixed oxide ceramics are one of the materials envisaged for americium transmutation in sodium fast neutron reactors. The advantage of such microsphere precursor compared to classical oxide powder is the diminution of the risk of fine dissemination which can be critical for the handling of highly radioactive powders such as americium based oxides and the improvement of flowability for the filling of compaction chamber. Those millimetric oxide microspheres incorporating uranium and americium were synthesized and characterizations showed a very porous microstructure very brittle in nature which occurred to be adapted to shaping by compaction. Studies allowed to determine an optimal heat treatment with calcination temperature comprised between 700-800 °C and temperature rate lower than 2 °C/min. Oxide Precursors were die-pressed into pellets and then sintered under air to form regular ceramic pellets of 95% of theoretical density (TD) and of homogeneous microstructure. This study validated thus the scientific feasibility of the CRMP process to prepare bearing americium target in a powder free manner.

  20. Assessment of some ion-exchangers for the treatment of low-level radioactive liquid waste solutions

    SciTech Connect

    El-Sourougy, M.R.; El-Dessouky, M.I.; Aly, H.F.

    1994-12-31

    Demineralization of potable water, as representative of LLLW was carried out using 8-different cationic and anionic ion-exchangers. The cationic exchangers used are: KY-2, Dowex50W-X8, Amberlite IR-120 and Chelex-100. The anionic exchangers are: AN-31, Amberlite IRA-900, Permutit and Dowex-3. Ion-exchanger dynamic capacity was calculated in terms of g.equivalent/kg of ion-exchanger. Different regeneration regimes were investigated and evaluated.

  1. Regeneration of strong-base anion-exchange resins by sequential chemical displacement

    DOEpatents

    Brown, Gilbert M.; Gu, Baohua; Moyer, Bruce A.; Bonnesen, Peter V.

    2002-01-01

    A method for regenerating strong-base anion exchange resins utilizing a sequential chemical displacement technique with new regenerant formulation. The new first regenerant solution is composed of a mixture of ferric chloride, a water-miscible organic solvent, hydrochloric acid, and water in which tetrachloroferrate anion is formed and used to displace the target anions on the resin. The second regenerant is composed of a dilute hydrochloric acid and is used to decompose tetrachloroferrate and elute ferric ions, thereby regenerating the resin. Alternative chemical displacement methods include: (1) displacement of target anions with fluoroborate followed by nitrate or salicylate and (2) displacement of target anions with salicylate followed by dilute hydrochloric acid. The methodology offers an improved regeneration efficiency, recovery, and waste minimization over the conventional displacement technique using sodium chloride (or a brine) or alkali metal hydroxide.

  2. Ion Exchange Modeling Of Cesium Removal From Hanford Waste Using Spherical Resorcinol-Formaldehyde Resin

    SciTech Connect

    Aleman, S.; Hamm, L.; Smith, F.

    2007-06-27

    This report discusses the expected performance of spherical Resorcinol-Formaldehyde (RF) ion exchange resin for the removal of cesium from alkaline Hanford radioactive waste. Predictions of full scale column performance in a carousel mode are made for the Hot Commissioning, Envelope B, and Subsequent Operations waste compositions under nominal operating conditions and for perturbations from the nominal. Only the loading phase of the process cycle is addressed in this report. Pertinent bench-scale column tests, kinetic experiments, and batch equilibrium experiments are used to estimate model parameters and to benchmark the ion-exchange model. The methodology and application presented in this report reflect the expected behavior of spherical RF resin manufactured at the intermediate-scale (i.e., approximately 100 gallon batch size; batch 5E-370/641). It is generally believed that scale-up to production-scale in resin manufacturing will result in similarly behaving resin batches whose chemical selectivity is unaffected while total capacity per gram of resin may vary some. As such, the full-scale facility predictions provided within this report should provide reasonable estimates of production-scale column performance.

  3. Phosphate recovery from wastewater using engineered superparamagnetic particles modified with layered double hydroxide ion exchangers.

    PubMed

    Drenkova-Tuhtan, Asya; Mandel, Karl; Paulus, Anja; Meyer, Carsten; Hutter, Frank; Gellermann, Carsten; Sextl, Gerhard; Franzreb, Matthias; Steinmetz, Heidrun

    2013-10-01

    An innovative nanocomposite material is proposed for phosphate recovery from wastewater using magnetic assistance. Superparamagnetic microparticles modified with layered double hydroxide (LDH) ion exchangers of various compositions act as phosphate adsorbers. Magnetic separation and chemical regeneration of the particles allows their reuse, leading to the successful recovery of phosphate. Based upon the preliminary screening of different LDH ion exchanger modifications for phosphate selectivity and uptake capacity, MgFe-Zr LDH coated magnetic particles were chosen for further characterization and application. The adsorption kinetics of phosphate from municipal wastewater was studied in dependence with particle concentration, contact time and pH. Adsorption isotherms were then determined for the selected particle system. Recovery of phosphate and regeneration of the particles was examined via testing a variety of desorption solutions. Reusability of the particles was demonstrated for 15 adsorption/desorption cycles. Adsorption in the range of 75-97% was achieved in each cycle after 1 h contact time. Phosphate recovery and enrichment was possible through repetitive application of the desorption solution. Finally, a pilot scale experiment was carried out by treating 125 L of wastewater with the particles in five subsequent 25 L batches. Solid-liquid separation on this scale was carried out with a high-gradient magnetic filter (HGMF).

  4. Modeling Ion-Exchange Processing With Spherical Resins For Cesium Removal

    SciTech Connect

    Hang, T.; Nash, C. A.; Aleman, S. E.

    2012-09-19

    The spherical Resorcinol-Formaldehyde and hypothetical spherical SuperLig(r) 644 ion-exchange resins are evaluated for cesium removal from radioactive waste solutions. Modeling results show that spherical SuperLig(r) 644 reduces column cycling by 50% for high-potassium solutions. Spherical Resorcinol Formaldehyde performs equally well for the lowest-potassium wastes. Less cycling reduces nitric acid usage during resin elution and sodium addition during resin regeneration, therefore, significantly decreasing life-cycle operational costs. A model assessment of the mechanism behind ''cesium bleed'' is also conducted. When a resin bed is eluted, a relatively small amount of cesium remains within resin particles. Cesium can bleed into otherwise decontaminated product in the next loading cycle. The bleed mechanism is shown to be fully isotherm-controlled vs. mass transfer controlled. Knowledge of residual post-elution cesium level and resin isotherm can be utilized to predict rate of cesium bleed in a mostly non-loaded column. Overall, this work demonstrates the versatility of the ion-exchange modeling to study the effects of resin characteristics on processing cycles, rates, and cold chemical consumption. This evaluation justifies further development of a spherical form of the SL644 resin.

  5. Extraction of Carbon Dioxide From Seawater by Ion Exchange Resin. Part 2. Using Strong Base Anion Exchange Resin

    DTIC Science & Technology

    2009-09-29

    Naval Research Laboratory Washington, DC 20375-5320 NRL/MR/6180--09-9211 Extraction of Carbon Dioxide from Sea water by Ion Exchange Resin Part...STRONG BASE ANION EXCHANGE RESIN 1.0 BACKGROUND The Ocean Thermal Energy Conversion (OTEC) process converts solar thermal energy absorbed by the ocean...into electrical power [1,2]. During the OTEC process dissolved carbon dioxide (CO2) in ocean water is liberated as a gas. Since CO2 is implicated in

  6. Preparation SnO₂ nanolayer on flexible polyimide substrates via direct ion-exchange and in situ oxidation process.

    PubMed

    Cui, Guanghui; Wu, Dezhen; Qi, Shengli; Jin, Shao; Wu, Zhanpeng; Jin, Riguang

    2011-03-01

    Tin oxide (SnO(2)) nanolayers were formed on flexible polyimide (PI) substrate via direct ion-exchange and in situ oxidation process utilizing pyromellitic dianhydride/4,4'-oxidianiline-based poly(amic acid) films as polyimide precursor. During an ion-exchange process, stannous ions were doped into the precursor by immersion in ethanolic solution of stannous chloride. Subsequent thermal treatment of the tin(II)-containing precursor at a constant heating rate not only imidized poly(amic acid) to PI but also converted stannous ions into SnO(2) clusters, which diffused and aggregated onto the surface of polymer matrix, forming continuous tin oxide layers. Inductively coupled plasma (ICP) was used to investigate the ion-exchange process. Changes in chemical structure of the poly(amic acid) film and the crystal structure of tin oxides were analyzed by attenuated total reflection-Fourier transform infrared (ATR-FTIR) and X-ray diffraction (XRD). Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to study the microstructure of the PI/SnO(2) nanocomposite films. The nanocomposite film maintained essential mechanical property and thermal stability of pristine PI films.

  7. Use of petroleum reside for production of ion exchangers

    SciTech Connect

    Pokonova, Y.V.

    1995-03-10

    Weakly acidic commercial cation exchangers with a static exchange capacity of 4.8-6.7 meq{center_dot}{sup -1} and a mechanical strength of 90% have been synthesized from petroleum asphaltites, resorcinol, and furfural.

  8. Kinetics of sorption of niobium ions by anion-exchangers from mixed chloride-fluoride solutions

    SciTech Connect

    Rychkov, V.N.; Pakholkov, V.S.; Kuznetsova, L.D.

    1987-08-10

    The authors showed earlier on the basis of experimental and calculated data obtained in studies of ion-exchange equilibrium that the sorbability and composition of sorbed niobium ions are determined by the content of hydrofluoric acid in mixed chloride-fluoride solutions. Variation of the ionic state of niobium in these solutions should also influence the rate of ion exchange. In this communication they examine the results of a study of the kinetics of exchange of niobium ions on AV-17 x 8, EDE-10P, and AN-2F anion-exchange resins in fluoride-containing solutions. Kinetic curves for sorption of niobium ions and the results of their evaluation are presented.

  9. Charge-exchange plasma environment for an ion drive spacecraft

    NASA Technical Reports Server (NTRS)

    Kaufman, H. R.; Carruth, M. R., Jr.

    1981-01-01

    A model was reviewed which describes the propagation of the mercury charge-exchange plasma and extended to describe the flow of the molybdenum component of the charge-exchange plasma. The uncertainties in the models for various conditions are discussed. Such topics as current drain to the solar array, charge-exchange plasma material deposition, and the effects of space plasma on the charge-exchange plasma propagation are addressed.

  10. Advantages of chemical exchange-sensitive spin-lock (CESL) over chemical exchange saturation transfer (CEST) for hydroxyl- and amine-water proton exchange studies.

    PubMed

    Jin, Tao; Kim, Seong-Gi

    2014-11-01

    The chemical exchange (CE) rate of endogenous hydroxyl and amine protons with water is often comparable to the difference in their chemical shifts. These intermediate exchange processes have been imaged by the CE saturation transfer (CEST) approach with low-power and long-duration irradiation. However, the sensitivity is not optimal and, more importantly, the signal is contaminated by slow magnetization transfer processes. Here, the properties of CEST signals are compared with those of a CE-sensitive spin-lock (CESL) technique irradiating at the labile proton frequency. First, using a higher power and shorter irradiation in CE-MRI, we obtain: (i) an increased selectivity to faster CE rates via a higher sensitivity to faster CEs and a lower sensitivity to slower CEs and magnetization transfer processes; and (ii) a decreased in vivo asymmetric magnetization transfer contrast measured at ±15 ppm. The sensitivity gain of CESL over CEST is higher for a higher power and shorter irradiation. Unlike CESL, CEST signals oscillate at a very high power and short irradiation. Second, time-dependent CEST and CESL signals are well modeled by analytical solutions of CE-MRI with an asymmetric population approximation, which can be used for quantitative CE-MRI and validated by simulations of Bloch-McConnell equations and phantom experiments. Finally, the in vivo amine-water proton exchange contrast measured at 2.5 ppm with ω1 = 500 Hz is 18% higher in sensitivity for CESL than CEST at 9.4 T. Overall, CESL provides better exchange rate selectivity and sensitivity than CEST; therefore, CESL is more suitable for CE-MRI of intermediate exchange protons.

  11. Introduction: Applying Chemical Biology to Ion Channels.

    PubMed

    Pless, Stephan A; Ahern, Christopher A

    2015-01-01

    Ion channels are membrane-spanning proteins that control the flow of ions across biological membranes through an aqueous pathway. The opening or closing of this pore can be controlled by a myriad of physiological inputs (voltage, ligands, temperature, metabolites, pH), which in turn allow for the controlled flux of ions across membranes, resulting in the generation of minute electrical signals. The functional implications of ion channel function on physiological processes are vast. Electrical impulses, in the form of action potentials or diverse chemo-electrical signals, coordinate the syncytium of the heart beat, support a myriad of neuronal communication pathways, insulin secretion, and are central to the immune response, with more roles being discovered virtually everyday. Thus, ion channel function is a biophysical process that is central to biological life at many levels. And with over 500 channel-forming subunits known today in humans, this large class of proteins is also increasingly recognised as important drug targets, as inherited or acquired ion channel dysfunction are known causes of disease.

  12. A comparative study of ion exchange kinetics in zinc/lead-modified zeolite-clinoptilolite systems.

    PubMed

    Trgo, M; Perić, J; Medvidović, N Vukojević

    2006-08-25

    The kinetics of zinc and lead ions removal by modified zeolite-clinoptilolite has been investigated. The rate of the ion exchange process for lead ions is faster than for zinc ions, as well as the time needed to reach the equilibrium. The ion exchange capacity of zeolite of lead ions is doubly higher than that of zinc ions. Diffusion models according to the Vermeulen's approximation, the parabolic diffusion model and the homogeneous diffusion model have been tested with the experimental data of ion exchange for zinc and lead. For both systems examined, the best fit of the models proposed with the experimental data was shown by the Vermeulen's approximation and the homogeneous diffusion model with t-->t(infinity). The diffusion coefficients are calculated from kinetic models of lead ions they are of the order of 10(-6)cm(2)/min, constant for all examined initial concentrations and not dependent on time. The diffusion coefficients in the system of zinc ions is of the order of 10(-8)cm(2)/min, also independent of initial concentrations, but decreasing with time from the beginning of ion exchange to the equilibrium.

  13. Chemical Exchange Saturation Transfer (CEST) Agents: Quantum Chemistry and MRI.

    PubMed

    Li, Jikun; Feng, Xinxin; Zhu, Wei; Oskolkov, Nikita; Zhou, Tianhui; Kim, Boo Kyung; Baig, Noman; McMahon, Michael T; Oldfield, Eric

    2016-01-04

    Diamagnetic chemical exchange saturation transfer (CEST) contrast agents offer an alternative to Gd(3+) -based contrast agents for MRI. They are characterized by containing protons that can rapidly exchange with water and it is advantageous to have these protons resonate in a spectral window that is far removed from water. Herein, we report the first results of DFT calculations of the (1) H nuclear magnetic shieldings in 41 CEST agents, finding that the experimental shifts can be well predicted (R(2) =0.882). We tested a subset of compounds with the best MRI properties for toxicity and for activity as uncouplers, then obtained mice kidney CEST MRI images for three of the most promising leads finding 16 (2,4-dihydroxybenzoic acid) to be one of the most promising CEST MRI contrast agents to date. Overall, the results are of interest since they show that (1) H NMR shifts for CEST agents-charged species-can be well predicted, and that several leads have low toxicity and yield good in vivo MR images.

  14. ION-EXCHANGE METHOD FOR SEPARATING RADIUM FROM RADIUM-BARIUM MIXTURES

    DOEpatents

    Fuentevilla, M.E.

    1959-06-30

    An improved process is presented for separating radium from an aqueous feed solution containing radium and barium values and a complexing agent for these metals. In this process a feed solutlon containing radium and barium ions and a complexing agent for said ions ls cycled through an exchange zone in resins. The radiumenriched resin is then stripped of radium values to form a regeneration liquid, a portion of which is collected as an enriched product, the remaining portion being recycled to the exchange zone to further enrich the ion exchange resin in radium.

  15. Ion exchange in the atomic energy industry with particular reference to actinide and fission product separation

    SciTech Connect

    Jenkins, I.L.

    1984-01-01

    Reviewed are some of the uses of ion exchange processes used by the nuclear industry for the period April, 1978 to April, 1983. The topics dealt with are: thorium, protactinium, uranium, neptunium, plutonium, americium, cesium and actinide-lanthanide separations; the higher actinides - Cm, Bk, Cf, Es and Fm; fission products; ion exchange in the geological disposal of radioactive waste. Consideration is given to safety in the use of ion exchangers and in safe methods of disposal of such materials. Full scale and pilot plant process descriptions are included as well as summaries of laboratory studies. 130 references.

  16. Valence parity renders z(*)-type ions chemically distinct.

    PubMed

    Hubler, Shane L; Jue, April; Keith, Jason; McAlister, Graeme C; Craciun, Gheorghe; Coon, Joshua J

    2008-05-21

    Here we report that the odd electron z (*) -type ions formed by the electron-based peptide dissociation methods (electron capture or transfer, ECD or ETD) have distinctive chemical compositions from other common product ion types. Specifically, b-, c-, and y-type ions have an odd number of atoms with an odd valence (e.g., N and H), while z (*)-type ions contain an even number of atoms with an odd valence. This tenet, referred to as the valence parity rule, mandates that no c-type ion shall have the same chemical composition, and by extension mass, as a z (*) -type ion. By experiment we demonstrate that nearly half of all observed c- and z (*) -type product ions resulting from 226 ETD product ion spectra can be assigned to a single, correct, chemical composition and ion type by simple inspection of the m/ z peaks. The assignments provide (1) a platform to directly determine amino acid composition, (2) an input for database search algorithms, or (3) a basis for de novo sequence analysis.

  17. Truly Incomplete and Complex Chromosomal Exchanges in Human Fibroblast Cells Exposed In Situ to Energetic Heavy Ions

    NASA Technical Reports Server (NTRS)

    Wu, Honglu; Durante, marco; Furusawa, Yoshiya; George, Kerry; Kawata, Tetsuya; Cucinotta, Francis A.

    2003-01-01

    Confluent human fibroblast cells (AG 1522) were irradiated with gamma rays, 490 MeV/nucleon Si, or with Fe ions at either 200 or 500 MeV/nucleon. The cells were allowed to repair at 37 C for 24 hours after exposure, and a chemically induced premature chromosome condensation (PCC) technique was used to condense chromosomes in the G2 phase of the cell cycle. Incomplete and complex exchanges were analyzed in the irradiated samples. In order to verify that chromosomal breaks were truly unrejoined, chromosome aberrations were analyzed using a combination of whole chromosome specific probes and probes specific for the telomere region of the chromosome. Results showed that the frequency of unrejoined chromosome breaks was higher after high-LET radiation, and consequently, the ratio of incomplete to complete exchanges increased steadily with LET up to 440 keV/micron, the highest LET value in the present study. For samples exposed to 200 MeV/nucleon Fe ions, chromosome aberrations were analyzed using the multicolor FISH (mFISH) technique that allow identification of both complex and truly incomplete exchanges. Results of the mFISH study showed that 0.7 and 3 Gy dose of the Fe ions produced similar ratios of complex to simple exchanges and incomplete to complete exchanges, values for which were higher than those obtained after a 6 Gy gamma exposure. After 0.7 Gy of Fe ions, most complex aberrations were found to involve three or four chromosomes, which is a likely indication of the maximum number of chromosome domains traversed by a single Fe ion track.

  18. Comprehensive chemical analyses of natural cordierites: implications for exchange mechanisms

    NASA Astrophysics Data System (ADS)

    Bertoldi, Christian; Proyer, Alexander; Garbe-Schönberg, Dieter; Behrens, Harald; Dachs, Edgar

    2004-12-01

    Cordierite samples from pegmatites and metamorphic rocks have been analysed for major [electron microprobe analysis (EMPA)] and trace elements [inductively coupled plasma mass spectrometry (ICP-MS), secondary ion mass spectrometry analyses (SIMS)] as well as for H 2O and CO 2 (coulometric titration), and the results evaluated in conjunction with published data in order to determine which exchange mechanisms are significant. Apart from the homovalent substitutions FeMg -1 and MnMg -1 on the octahedral site, some minor KNa -1 on the Ch0 channel site, and Fe 3+Al -1 on the T 11 tetrahedral site, the three most important substitution mechanisms are those for the incorporation of Li on the octahedral sites (NaLi□ -1Mg -1), and of Be and other divalent cations on the tetrahedral T 11 site (NaBe□ -1Al -1 and Na(Mg,Fe 2+)□ -1Al -1). The dominant role of the last vector is clearly demonstrated. We propose a new generalized formula for cordierite: Ch(Na,K) 0-1VI(Mg,Fe 2+,Mn,Li) 2IVSi 5IVAl 3IV(Al, Be, Mg, Fe 2+, Fe 3+)O 18 * xCh(H 2O, CO 2…). Our results show that the population of (Mg, Fe 2+) on the T 11-site is limited to about 0.08 a.p.f.u. Other exchange mechanisms that were encountered in experiments operate only under P- T conditions or in bulk compositions that are rarely realized in nature. Routine analyses by electron microprobe in which Li and Be are not determined can be plotted as (Mg+Fe+Mn) versus (Si+Al) to assess whether significant amounts of Li and Be could be present. These amounts can be calculated as Li (a.p.f.u.)=Al+Na-4 and Be (a.p.f.u.)=10-2Al-M 2+-Na.

  19. Effects of magnetic ion-exchange resin addition during coagulation on floc properties and membrane filtration.

    PubMed

    Choi, Yang Hun; Kweon, Ji Hyang; Jeong, Young Mi; Kwon, Soonbuhm; Kim, Hyung-Soo

    2010-03-01

    The application of magnetic ion-exchange resin (MIEX) during chemical coagulation was investigated for the removal of organic matters responsible for fouling in membrane processes. Two different coagulants were used-polyaluminium chloride (PAC1) and polyaluminum chloride silicate (PACS). The MIEX addition during coagulation with both PAC1 and PACS considerably enhanced removal of dissolved organic carbon. Coagulation with MIEX treatment substantially removed all portions of natural organic matter (NOM), while the MIEX treatment alone effectively removed the hydrophobic and transphilic portions of NOM. The enhanced NOM removal by PAC1 coagulation with the addition of MIEX had positive effects on membrane flux at moderate transmembrane pressure conditions. However, the almost identical flux patterns were reported in the experiments of coagulation with PACS and PACS with MIEX addition. The results of the specific cake resistances indicated that the MIEX addition substantially decreased the resistances. The larger size distributions of PAC1 with MIEX corresponded well with the flux improvement.

  20. Heterogeneous structure and its effect on properties and electrochemical behavior of ion-exchange membrane

    NASA Astrophysics Data System (ADS)

    Ariono, D.; Khoiruddin; Subagjo; Wenten, I. G.

    2017-02-01

    Generally, commercially available ion-exchange membrane (IEM) can be classified into homogeneous and heterogeneous membranes. The classification is based on degree of heterogeneity in membrane structure. It is well known that the heterogeneity greatly affects the properties of IEM, such as conductivity, permselectivity, chemical and mechanical stability. The heterogeneity also influences ionic and electrical current transfer behavior of IEM-based processes during their operation. Therefore, understanding the role of heterogeneity in IEM properties is important to provide preliminary information on their operability and applicability. In this paper, the heterogeneity and its effect on IEM properties are reviewed. Some models for describing the heterogeneity of IEM and methods for characterizing the degree of heterogeneity are discussed. In addition, the influence of heterogeneity on the performance of IEM-based processes and their electrochemical behavior are described.

  1. Tramadol loading, release and iontophoretic characteristics of ion-exchange fiber.

    PubMed

    Gao, Yanan; Yuan, Jing; Liu, Hongzhuo; Yang, Yang; Hou, Yanlong; Li, Sanming

    2014-04-25

    The objective of this study was to investigate the drug loading, release and iontophoretic characteristics of strong acidic ion-exchange fiber, using tramadol hydrochloride as a model drug. The complex of charged model drug and ion-exchange fiber was studied as a new approach to achieve controlled drug delivery. Structural characterization of the fiber was elucidated through different approaches including differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), scanning electron microscope (SEM) and infrared spectroscopy (IR). And the mechanism of drug binding into ion-exchange fibers was validated to be ion-exchange. The drug loading into and release from ion-exchange fiber were affected by the concentration, volume and valence of the counter-ions in the external solution. Iontophoresis could significantly increase the delivery rate and amount of transdermal drug, and the iontophoretic dose could be easily controlled by adjusting the current intensity and the amount of release medium. The tramadol could be steadily released both from the drug-loaded fiber and drug solution when applied the iontophoretic method, which was in disagreement with the previous publications. As a drug reservoir, ion-exchange fiber has good regularity of drug loading, release and iontophoretic characteristics.

  2. Enhanced capacity and stability for the separation of cesium in electrically switched ion exchange

    SciTech Connect

    Tawfic, A.F.; Dickson, S.E.; Kim, Y.; Mekky, W.

    2015-03-15

    Electrically switched ion exchange (ESIX) can be used to separate ionic contaminants from industrial wastewater, including that generated by the nuclear industry. The ESIX method involves sequential application of reduction and oxidation potentials to an ion exchange film to induce the respective loading and unloading of cesium. This technology is superior to conventional methods (e.g electrodialysis reversal or reverse osmosis) as it requires very little energy for ionic separation. In previous studies, ESIX films have demonstrated relatively low ion exchange capacities and limited film stabilities over repeated potential applications. In this study, the methodology for the deposition of electro-active films (nickel hexacyanoferrate) on nickel electrodes was modified to improve the ion exchange capacity for cesium removal using ESIX. Cyclic voltammetry was used to investigate the ion exchange capacity and stability. Scanning electron microscopy (SEM) was used to characterize the modified film surfaces. Additionally, the films were examined for the separation of cesium ions. This modified film preparation technique enhanced the ion exchange capacity and improves the film stability compared to previous methods for the deposition of ESIX films. (authors)

  3. Solvent Influenced Fluxionality Studied by Ultrafast Chemical Exchange Spectroscopy

    NASA Astrophysics Data System (ADS)

    Ross, Matthew; Kubarych, Kevin

    2012-02-01

    Two-dimensional infrared spectroscopy (2DIR) allows unprecedentedly detailed understanding of the dynamics of chemical systems in the condensed phase. Carbonyl vibrations of small transition metal complexes report intramolecular dynamics and solvent-solute interactions due to their strong oscillator strengths and moderate environmental sensitivity. We studed the fluxional dynamics of iron pentacarbonyl (Fe(CO)5), which is unique in that it contains nearly perfectly uncoupled vibrational modes. We seek to probe the ``molecularity'' of condensed phase activated barrier crossings beyond the continuum Kramers theory picture. Using 2DIR chemical exchange spectroscopy, we show how the dynamics of Berry pseudorotation, the only significant mechanism for vibrational mode mixing on our experimental timescale, is sensitive to interactions with the environment. In a wide range of solvents, we have investigated the effects of hydrogen bonding with alcohols and friction from high viscosity alkanes. In addition, we have monitored vibrational energy redistribution as a solvation shell probe. Moreover, recently implemented mid-infrared pulse shaper based methods allow increased flexibility in experimental design, enabling experimental techniques that are not possible using passive optics.

  4. Mechanical and chemical effects of ion-texturing biomedical polymers

    NASA Technical Reports Server (NTRS)

    Weigand, A. J.; Cenkus, M. A.

    1979-01-01

    To determine whether sputter etching may provide substantial polymer surface texturing with insignificant changes in chemical and mechanical properties, an 8 cm beam diameter, electron bombardment, argon ion source was used to sputter etch (ion-texture process) nine biomedical polymers. The materials included silicone rubber, 32% carbon impregnated polyolefin, polyoxymethylene, polytetrafluoroethylene, ultrahigh molecular weight (UHMW) polyethylene, UHMW polyethylene with carbon fibers (10%), and several polyurethanes (bioelectric, segmented, and cross linked). Ion textured microtensile specimens of each material except UHMW polyethylene and UHMW polyethylene with 10% carbon fibers were used to determine the effect of ion texturing on tensile properties. Scanning electron microscopy was used to determine surface morphology changes, and electron spectroscopy for chemical analysis was used to analyze the near surface chemical changes that result from ion texturing. Ion energies of 500 eV with beam current densities ranging from 0.08 to 0.19 mA/sq cm were used to ion texture the various materials. Standard microtensile specimens of seven polymers were exposed to a saline environment for 24 hours prior to and during the tensile testing. The surface chemical changes resulting from sputter etching are minimal in spite of the often significant changes in the surface morphology.

  5. Electrochemical acidification of Kraft black liquor by electrodialysis with bipolar membrane: Ion exchange membrane fouling identification and mechanisms.

    PubMed

    Haddad, Maryam; Mikhaylin, Sergey; Bazinet, Laurent; Savadogo, Oumarou; Paris, Jean

    2017-02-15

    Integrated forest biorefinery offers promising pathways to sustainably diversify the revenue of pulp and paper industry. In this context, lignin can be extracted from a residual stream of Kraft pulping process, called black liquor, and subsequently converted into a wide spectrum of bio-based products. Electrochemical acidification of Kraft black liquor by electrodialysis with bipolar membrane results in lignin extraction and caustic soda production. Even though the implementation of this method requires less chemicals than the chemical acidification process, fouling of the ion exchange membranes and especially bipolar membrane impairs its productivity. Membrane thickness and ash content measurements along with scanning electron microscopy (SEM), elemental analysis (EDX) and X-ray photoelectron spectrometry (XPS) analysis were performed to identify the nature and mechanisms of the membrane fouling. The results revealed that the fouling layer mostly consisted of organic components and particularly lignin. Based on our proposed fouling mechanisms, throughout the electrodialysis process the pH of the black liquor gradually decreased and as a result more proton ions were available to trigger protonation reaction of lignin phenolic groups and decrease the lignin solubility. Due to the abundance of the proton ions on the surface of the cation exchange layers of the bipolar membrane, destabilized lignin macro-molecules started to self-aggregate and formed lignin clusters on its surface. Over the time, these lignin clusters covered the entire surface of the bipolar membrane and the spaces between the membranes and, eventually, attached to the surface of the cation exchange membrane.

  6. Reach-scale cation exchange controls on major ion chemistry of an Antarctic glacial meltwater stream

    USGS Publications Warehouse

    Gooseff, Michael N.; McKnight, Diane M.; Runkel, Robert L.

    2004-01-01

    McMurdo dry valleys of Antarctica represent the largest of the ice-free areas on the Antarctic continent, containing glaciers, meltwater streams, and closed basin lakes. Previous geochemical studies of dry valley streams and lakes have addressed chemical weathering reactions of hyporheic substrate and geochemical evolution of dry valley surface waters. We examine cation transport and exchange reactions during a stream tracer experiment in a dry valley glacial meltwater stream. The injection solution was composed of dissolved Li+, Na+, K+, and Cl-. Chloride behaved conservatively in this stream, but Li+, Na+, and K+ were reactive to varying degrees. Mass balance analysis indicates that relative to Cl-, Li+ and K+ were taken up in downstream transport and Na+ was released. Simulations of conservative and reactive (first-order uptake or generation) solute transport were made with the OTIS (one-dimensional solute transport with inflow and storage) model. Among the four experimental reaches of Green Creek, solute transport simulations reveal that Li+ was removed from stream water in all four reaches, K+ was released in two reaches, taken up in one reach, and Na+ was released in all four reaches. Hyporheic sediments appear to be variable with uptake of Li+ in two reaches, uptake of K+ in one reach, release of K+ in two reaches, and uptake of Na+ in one reach. Mass balances of the conservative and reactive simulations show that from 1.05 to 2.19 moles of Li+ was adsorbed per reach, but less than 0.3 moles of K+ and less than 0.9 moles of Na+ were released per reach. This suggests that either (1) exchange of another ion which was not analyzed in this experiment or (2) that both ion exchange and sorption control inorganic solute transport. The elevated cation concentrations introduced during the experiment are typical of initial flows in each flow season, which flush accumulated dry salts from the streambed. We propose that the bed sediments (which compose the hyporheic

  7. Studies of composite ion exchange membranes formed from gamma radiation initiated formed from gamma radiation initiated grafting of polymers to modified expanded teflon membranes

    SciTech Connect

    Blubaugh, E.A.; Ramos, B.L.; Heineman, W.R.

    1995-12-31

    This report will present our results for evaluating expanded Teflon as a matrix for polymer grafting. The porosity of the ePTFE starting material was kept constant. However, the volume percent of monomer to solvent and the radiation dosage levels were varied. Also, the monomers used were styrene and (2-dimethylaminoethyl methacrylate) and the influence on the microscopic characteristics of the composite polymers was evaluated via gravimetric determinations and Scanning Electron Microscopy (SEM), respectively. The grafted polystyrene or poly-(2-dimethylaminoethyl methacrylate) must be further modified chemically. The polystyrene must be sulfonated and the poly-(2-dimethylaminoethyl methacrylate) must be quatemized via 2-Bromobutane. These chemical modifications convert the polystyrene into polystyrene-sulfonate (a cation exchanger) and the conversion of poly-(2-dimethylaminoethyl methacrylate) to poly-(2-dimethyl-butyl ammonium ethyl methacrylate) bromide (an anion exchange medium). These polymer composites were evaluated as to their ion-exchange ability, via the electrochemical activity displayed through exchanged electroactive ions.

  8. Kinetics of oxygen exchange between bisulfite ion and water as studied by oxygen-17 nuclear magnetic resonance spectroscopy

    SciTech Connect

    Horner, D.A.

    1984-08-01

    The nuclear magnetic relaxation times of oxygen-17 have been measured in aqueous sodium bisulfite solutions in the pH range from 2.5 to 5 as a function of temperature, pH, and S(IV) concentration, at an ionic strength of 1.0 m. The rate law for oxygen exchange between bisulfite ion and water was obtained from an analysis of the data, and is consistent with oxygen exchange occurring via the reaction SO/sub 2/ + H/sub 2/O right reversible H/sup +/ + SHO/sub 3//sup -/. The value of k/sub -1/ is in agreement with relaxation measurements. Direct spectroscopic evidence was found for the existence of two isomers of bisulfite ion: one with the proton bonded to the sulfur (HSO/sub 3//sup -/) and the other with the proton bonded to an oxygen (SO/sub 3/H/sup -/). (The symbol SHO/sub 3//sup -/ in the above chemical equation refers to both isomeric forms of bisulfite ion.) The relative amounts of the two isomers were determined as a function of temperature, and the rate and mechanism of oxygen exchange between the two was investigated. One of the two isomers, presumably SO/sub 3/H/sup -/, exchanges oxygens with water much more rapidly than does the other. A two-pulse sequence was developed which greatly diminished the solvent peak in the NMR spectrum.

  9. Tuning a High Transmission Ion Guide to Prevent Gas-Phase Proton Exchange During H/D Exchange MS Analysis.

    PubMed

    Guttman, Miklos; Wales, Thomas E; Whittington, Dale; Engen, John R; Brown, Jeffery M; Lee, Kelly K

    2016-04-01

    Hydrogen/deuterium exchange (HDX) mass spectrometry (MS) for protein structural analysis has been adopted for many purposes, including biopharmaceutical development. One of the benefits of examining amide proton exchange by mass spectrometry is that it can readily resolve different exchange regimes, as evidenced by either binomial or bimodal isotope patterns. By careful analysis of the isotope pattern during exchange, more insight can be obtained on protein behavior in solution. However, one must be sure that any observed bimodal isotope patterns are not artifacts of analysis and are reflective of the true behavior in solution. Sample carryover and certain stationary phases are known as potential sources of bimodal artifacts. Here, we describe an additional undocumented source of deuterium loss resulting in artificial bimodal patterns for certain highly charged peptides. We demonstrate that this phenomenon is predominantly due to gas-phase proton exchange between peptides and bulk solvent within the initial stages of high-transmission conjoined ion guides. Minor adjustments of the ion guide settings, as reported here, eliminate the phenomenon without sacrificing signal intensity. Such gas-phase deuterium loss should be appreciated for all HDX-MS studies using such ion optics, even for routine studies not focused on interpreting bimodal spectra. Graphical Abstract ᅟ.

  10. Chemical exchange in the interior of water-rich exoplanets

    NASA Astrophysics Data System (ADS)

    Tobie, G.; Choblet, G.; Grasset, O.

    2015-10-01

    Since the discovery of the first exoplanet in 1995 [1], the number of detected exoplanets has grown nearly exponentially [2]. We have learnt from the existing dataset that our Solar System is rather unusual. Exoplanet surveys revealed notably that exoplanets intermediate between Earth and Neptune are surprisingly common, while notably absent in the Solar System [3]. Model mass-radius relationships indicate a great diversity of interior composition and atmospheric extent for the Super-Earth/Mini- Neptune-planet class [e.g. 4]. The observed continuum between Earth-sized and Neptune-sized planets challenges our understanding of planet formation and evolution, which has been biased for many years by our vision of the Solar System. Planetary worlds are probably much more diverse than originally thought, with a wide range of water and other volatile content. In the Solar System, there is a strong dichotomy between the inner system with dry planetary objects having a very small volatile fraction (<0.1 %), and the outer solar system where water ice constitutes a large fraction of solid phase (> 20%). The volatile contents among other systems likely vary more gradually, and a large fraction of exoplanets with sizes intermediate between Earth and Neptune may have a water content exceeding several percents. The existence of massive water envelops around these planets may significantly affect the internal evolution and chemical exchanges between the deep interior and the atmosphere [e.g. 5]. Due to the very high-pressure expected inside these water-rich planets, especially for the the most massive ones, most of the water will be in the form of a high-pressure ice phase (ice VII) [6,7], the presence of liquid water being limited only to the first kilometres. The thermal structure and dynamics of these thick icy mantles are expected to control the heat and chemical transport from the silicate-rich interior to the surface [8,9], in a way analogous to the internal processes

  11. Method of detecting defects in ion exchange membranes of electrochemical cells by chemochromic sensors

    DOEpatents

    Brooker, Robert Paul; Mohajeri, Nahid

    2016-01-05

    A method of detecting defects in membranes such as ion exchange membranes of electrochemical cells. The electrochemical cell includes an assembly having an anode side and a cathode side with the ion exchange membrane in between. In a configuration step a chemochromic sensor is placed above the cathode and flow isolation hardware lateral to the ion exchange membrane which prevents a flow of hydrogen (H.sub.2) between the cathode and anode side. The anode side is exposed to a first reactant fluid including hydrogen. The chemochromic sensor is examined after the exposing for a color change. A color change evidences the ion exchange membrane has at least one defect that permits H.sub.2 transmission therethrough.

  12. Ion-exchange chromatography separation applied to mineral recycle in closed systems

    NASA Technical Reports Server (NTRS)

    Ballou, E.; Spitze, L. A.; Wong, F. W.; Wydeven, T.; Johnson, C. C.

    1981-01-01

    As part of the controlled ecological life support system (CELSS) program, a study is being made of mineral separation on ion-exchange columns. The purpose of the mineral separation step is to allow minerals to be recycled from the oxidized waste products of plants, man, and animals for hydroponic food production. In the CELSS application, relatively large quantities of minerals in a broad concentration range must be recovered by the desired system, rather than the trace quantities and very low concentrations treated in analytical applications of ion-exchange chromatography. Experiments have been carried out to assess the parameters pertinent to the scale-up of ion-exchange chromatography and to determine feasibility. Preliminary conclusions are that the column scale-up is in a reasonable size range for the CELSS application. The recycling of a suitable eluent, however, remains a major challenge to the suitability of using ion exchange chromatography in closed systems.

  13. The Determination of Calcium in Dietary Supplement Tablets by Ion-Exchange.

    ERIC Educational Resources Information Center

    Dietz, Mark L.

    1986-01-01

    An experimental simple ion-exchange experiment in which the amount of calcium present in dietary supplement tablets has been developed is described and some typical student results for several brands of tablets are presented. (JN)

  14. Removal of heavy metals from oil sludge using ion exchange textiles.

    PubMed

    Elektorowicz, M; Muslat, Z

    2008-04-01

    Development of a new simple and economic method for heavy-metal removal from oil sludge using ion exchange textiles was the main objective of this research. Three experimental stages were developed for this purpose using the bottom tank oil sludge from the Shell Canada refinery in Montreal, Canada. The first stage consisted of the direct application of ion exchange to oil sludge. The second stage included the pretreatment of oil sludge with organic solvents prior to the application of ion exchange process. The third stage included the pretreatment of oil sludge with an aqueous solution in order to extract heavy metals to the aqueous phase and then apply ion exchange textiles to the aqueous phase. Best results were obtained when acetone was used as an organic solvent leading to a total removal of vanadium while cadmium, zinc, nickel, iron, copper by 99%; 96%; 94%; 92% and 89%, respectively.

  15. Removal of uranium, arsenic, and nitrate by continuously regenerated ion exchange process

    SciTech Connect

    Chang, D.; Awad, J.; Panahi, Z.

    1996-11-01

    Groundwater is the major source of water supply for the City of Riverside (the City). Groundwater from some of the local wells contains high levels of uranium, arsenic, and nitrate. The City is evaluating treatment technologies that can remove these contaminants, in order to be prepared to select appropriate treatment technologies when groundwater treatment is required. Treatment technologies identified by the USEPA as best available technology (BAT) for uranium and arsenic removal are coagulation/filtration, lime softening, ion exchange, and reverse osmosis. Among these technologies, ion exchange is the most cost-effective and suitable for wellhead treatment applications. Ion exchange is also effective for nitrate removal. An ion exchange pilot study was conducted for the removal of uranium, arsenic and nitrate from groundwater. This paper presents a summary of the tests results, conceptual design criteria, and preliminary cost estimate for a full-scale facility.

  16. MODELING AN ION EXCHANGE PROCESS FOR CESIUM REMOVAL FROM ALKALINE RADIOACTIVE WASTE SOLUTIONS

    SciTech Connect

    Smith, F; Luther Hamm, L; Sebastian Aleman, S; Johnston Michael, J

    2008-08-26

    The performance of spherical Resorcinol-Formaldehyde ion-exchange resin for the removal of cesium from alkaline radioactive waste solutions has been investigated through computer modeling. Cesium adsorption isotherms were obtained by fitting experimental data using a thermodynamic framework. Results show that ion-exchange is an efficient method for cesium removal from highly alkaline radioactive waste solutions. On average, two 1300 liter columns operating in series are able to treat 690,000 liters of waste with an initial cesium concentration of 0.09 mM in 11 days achieving a decontamination factor of over 50,000. The study also tested the sensitivity of ion-exchange column performance to variations in flow rate, temperature and column dimensions. Modeling results can be used to optimize design of the ion exchange system.

  17. High Level Waste System Impacts from Small Column Ion Exchange Implementation

    SciTech Connect

    McCabe, D. J.; Hamm, L. L.; Aleman, S. E.; Peeler, D. K.; Herman, C. C.; Edwards, T. B.

    2005-08-18

    The objective of this task is to identify potential waste streams that could be treated with the Small Column Ion Exchange (SCIX) and perform an initial assessment of the impact of doing so on the High-Level Waste (HLW) system. Design of the SCIX system has been performed as a backup technology for decontamination of High-Level Waste (HLW) at the Savannah River Site (SRS). The SCIX consists of three modules which can be placed in risers inside underground HLW storage tanks. The pump and filter module and the ion exchange module are used to filter and decontaminate the aqueous tank wastes for disposition in Saltstone. The ion exchange module contains Crystalline Silicotitanate (CST in its engineered granular form is referred to as IONSIV{reg_sign} IE-911), and is selective for removal of cesium ions. After the IE-911 is loaded with Cs-137, it is removed and the column is refilled with a fresh batch. The grinder module is used to size-reduce the cesium-loaded IE-911 to make it compatible with the sludge vitrification system in the Defense Waste Processing Facility (DWPF). If installed at the SRS, this SCIX would need to operate within the current constraints of the larger HLW storage, retrieval, treatment, and disposal system. Although the equipment has been physically designed to comply with system requirements, there is also a need to identify which waste streams could be treated, how it could be implemented in the tank farms, and when this system could be incorporated into the HLW flowsheet and planning. This document summarizes a preliminary examination of the tentative HLW retrieval plans, facility schedules, decontamination factor targets, and vitrified waste form compatibility, with recommendations for a more detailed study later. The examination was based upon four batches of salt solution from the currently planned disposition pathway to treatment in the SCIX. Because of differences in capabilities between the SRS baseline and SCIX, these four batches were

  18. Combining ion mobility spectrometry with hydrogen-deuterium exchange and top-down MS for peptide ion structure analysis.

    PubMed

    Khakinejad, Mahdiar; Kondalaji, Samaneh Ghassabi; Maleki, Hossein; Arndt, James R; Donohoe, Gregory C; Valentine, Stephen J

    2014-12-01

    The gas-phase conformations of electrosprayed ions of the model peptide KKDDDDIIKIIK have been examined by ion mobility spectrometry (IMS) and hydrogen deuterium exchange (HDX)-tandem mass spectrometry (MS/MS) techniques. [M+4H](4+) ions exhibit two conformers with collision cross sections of 418 Å(2) and 471 Å(2). [M+3H](3+) ions exhibit a predominant conformer with a collision cross section of 340 Å(2) as well as an unresolved conformer (shoulder) with a collision cross section of ~367 Å(2). Maximum HDX levels for the more compact [M+4H](4+) ions and the compact and partially-folded [M+3H](3+) ions are ~12.9, ~15.5, and ~14.9, respectively. Ion structures obtained from molecular dynamics simulations (MDS) suggest that this ordering of HDX level results from increased charge-site/exchange-site density for the more compact ions of lower charge. Additionally, a new model that includes two distance calculations (charge site to carbonyl group and carbonyl group to exchange site) for the computer-generated structures is shown to better correlate to the experimentally determined per-residue deuterium uptake. Future comparisons of IMS-HDX-MS data with structures obtained from MDS are discussed with respect to novel experiments that will reveal the HDX rates of individual residues.

  19. Combining Ion Mobility Spectrometry with Hydrogen-Deuterium Exchange and Top-Down MS for Peptide Ion Structure Analysis

    NASA Astrophysics Data System (ADS)

    Khakinejad, Mahdiar; Kondalaji, Samaneh Ghassabi; Maleki, Hossein; Arndt, James R.; Donohoe, Gregory C.; Valentine, Stephen J.

    2014-12-01

    The gas-phase conformations of electrosprayed ions of the model peptide KKDDDDIIKIIK have been examined by ion mobility spectrometry (IMS) and hydrogen deuterium exchange (HDX)-tandem mass spectrometry (MS/MS) techniques. [M+4H]4+ ions exhibit two conformers with collision cross sections of 418 Å2 and 471 Å2. [M+3H]3+ ions exhibit a predominant conformer with a collision cross section of 340 Å2 as well as an unresolved conformer (shoulder) with a collision cross section of ~367 Å2. Maximum HDX levels for the more compact [M+4H]4+ ions and the compact and partially-folded [M+3H]3+ ions are ~12.9, ~15.5, and ~14.9, respectively. Ion structures obtained from molecular dynamics simulations (MDS) suggest that this ordering of HDX level results from increased charge-site/exchange-site density for the more compact ions of lower charge. Additionally, a new model that includes two distance calculations (charge site to carbonyl group and carbonyl group to exchange site) for the computer-generated structures is shown to better correlate to the experimentally determined per-residue deuterium uptake. Future comparisons of IMS-HDX-MS data with structures obtained from MDS are discussed with respect to novel experiments that will reveal the HDX rates of individual residues.

  20. Engineered ion channels as emerging tools for chemical biology.

    PubMed

    Mayer, Michael; Yang, Jerry

    2013-12-17

    Over the last 25 years, researchers have developed exogenously expressed, genetically engineered, semi-synthetic, and entirely synthetic ion channels. These structures have sufficient fidelity to serve as unique tools that can reveal information about living organisms. One of the most exciting success stories is optogenetics: the use of light-gated channels to trigger action potentials in specific neurons combined with studies of the response from networks of cells or entire live animals. Despite this breakthrough, the use of molecularly engineered ion channels for studies of biological systems is still in its infancy. Historically, researchers studied ion channels in the context of their own function in single cells or in multicellular signaling and regulation. Only recently have researchers considered ion channels and pore-forming peptides as responsive tools to report on the chemical and physical changes produced by other biochemical processes and reactions. This emerging class of molecular probes has a number of useful characteristics. For instance, these structures can greatly amplify the signal of chemical changes: the binding of one molecule to a ligand-gated ion channel can result in flux of millions of ions across a cell membrane. In addition, gating occurs on sub-microsecond time scales, resulting in fast response times. Moreover, the signal is complementary to existing techniques because the output is ionic current rather than fluorescence or radioactivity. And finally, ion channels are also localized at the membrane of cells where essential processes such as signaling and regulation take place. This Account highlights examples, mostly from our own work, of uses of ion channels and pore-forming peptides such as gramicidin in chemical biology. We discuss various strategies for preparing synthetically tailored ion channels that range from de novo designed synthetic molecules to genetically engineered or simply exogenously expressed or reconstituted wild

  1. Breadboard wash water renovation system. [using ferric chloride and ion exchange resins to remove soap and dissolved salts

    NASA Technical Reports Server (NTRS)

    1978-01-01

    A total wash water renovation system concept was developed for removing objectionable materials from spacecraft wash water in order to make the water reusable. The breadboard model system described provides for pretreatment with ferric chloride to remove soap by chemical precipitation, carbon adsorption to remove trace dissolved organics, and ion exchange for removal of dissolved salts. The entire system was put into continuous operation and carefully monitored to assess overall efficiency and equipment maintenance problems that could be expected in actual use. In addition, the capacity of the carbon adsorbers and the ion-exchange resin was calculated and taken into consideration in the final evaluation of the system adequacy. The product water produced was well within the Tentative Wash Water Standards with regard to total organic carbon, conductivity, urea content, sodium chloride content, color, odor, and clarity.

  2. Experimental Ion Exchange Column With SuperLig 639 And Simulant Formulation

    SciTech Connect

    Morse, Megan; Nash, C.

    2013-08-26

    SuperLig®639 ion exchange resin was tested as a retrieval mechanism for pertechnetate, through decontamination of a perrhenate spiked 5M Simple Average Na{sup +} Mass Based Simulant. Testing included batch contacts and a three-column ion exchange campaign. A decontamination of perrhenate exceeding 99% from the liquid feed was demonstrated. Analysis of the first formulation of a SBS/WESP simulant found unexpectedly low concentrations of soluble aluminum. Follow-on work will complete the formulation.

  3. Lawps ion exchange column gravity drain of spherical resorcinol formaldehyde resin

    SciTech Connect

    Duignan, M. R.; Herman, D. T.; Restivo, M. L.; Burket, P. R.

    2016-01-28

    Experiments at several different scales were performed to understand the removal of spherical resorcinol formaldehyde (sRF) ion exchange resin using a gravity drain system with a valve located above the resin screen in the ion exchange column (IXC). This is being considered as part of the design for the Low Activity Waste Pretreatment System (LAWPS) to be constructed at the DOE Hanford Site.

  4. Technology transfer: Ion exchange resins for Technetium-99 removal from X-705 raffinates

    SciTech Connect

    Deacon, L.E.; Greiner, M.J.

    1982-12-03

    An ion exchange process will be used at Portsmouth to remove Technetium-99 from uranium recovery waste solutions (raffinates). Subsequent treatment will then remove nitrates from the raffinates by a biodenitrification process prior to discharge to receiving streams to meet environmental standards for liquid wastes. Ion exchange process parameters affecting safe and efficient raffinate treatment have been examined in the laboratory, and results are described in this report. 4 refs., 3 figs., 6 tabs.

  5. Conversion of ion exchange resin to various functional resins and the application in the field of pharmaceutical sciences

    NASA Astrophysics Data System (ADS)

    Nakayama, Morio

    Ion exchange resins are widely used for separating ions in the solution, desalination, removal of impurities, and etc. Giving a new function to these ion exchange resins enables the application in more various fields. Until now, we carried out the research work about the following 5 project.: (1) Conversion of ion exchange resins into selective adsorbents by using low molecular reagents, which possess capabilities of a selective reaction with target ions, ion exchange reaction with the ion exchange resin and strong physical adsorption to the ion exchange resin. (2) Synthesis of resins for ion exchange high performance liquid chromatography (IEHPLC) and the analysis of biomaterials. (3) Development of insoluble macromolecular Sn(II) complex based on the aminophosphonic acid type ion exchange resin and its application to the 99mTc labeling of proteins. (4) Development of a new 68Ge-68Ga generator using N-methylglucamine type organic polymer as the adsorbent for 68Ge and production of 68Ga for PET. (5) Preparation of an ion-exchangeable polymer bead wrapped with bilayer membrane structures. In this paper, the application of various functional resins prepared based on ion exchange resin in the field of pharmaceutical sciences has been summarized.

  6. Unified Ion-chemical Model for the Middle Atmosphere

    NASA Astrophysics Data System (ADS)

    Kamsali, Nagaraja; Kamsali, Nagaraja; Datta, Jayati; Prasad, Bsn

    The importance of ion-chemical model studies in our understanding of middle atmospheric regions needs no special emphasis. Present day knowledge of middle atmosphere (0-100 km) has come from two distinct experimental developments: first, in situ measurements of ion composition by balloons and sounding rockets and second, laboratory investigations on ionchemical reactions of importance at these heights, determination of reaction rate coefficients and their temperature dependence. Model studies act as an interface between these, to generate theoretical estimates of ion composition and their derivatives (e.g. electrical conductivity) by using as input the laboratory data on reaction rate coefficients and the data on neutral species density, ionization flux, temperature etc. Free electrons exist only in the mesosphere. Positive molecular ions dominate the upper mesospheric heights and heavy positive and negative cluster ions appearing at the lower mesospheric heights continue to dominate in strato and troposphere. The equilibrium density of electrons and ionic species is governed by: a) ionization of the atmospheric constituents producing electron-positive ion pair b)gas-phase ion-chemical reactions that convert the electrons and primary positive ions into heavy cluster ions of both polarity c)heterogeneous ion-chemical reactions for producing aerosol ions and d) loss mechanisms for small ions and aerosol ions through recombination of oppositely charged species. Physical entities that control the ion production and loss processes are not the same and vary vastly both in nature and magnitude in the middle atmosphere X-rays, Lymann-alpha and precipitating electrons are the dominant ionizing agents at the mesospheric heights. Cosmic ray ionization that is not so significant in the mesosphere is the sole ionizing agent at stratosphere and troposphere. At the ground level and up to a few tens of meters above the earth's surface, natural radioactivity induced ionization is

  7. Assessment of commercially available ion exchange materials for cesium removal from highly alkaline wastes

    SciTech Connect

    Brooks, K.P.; Kim, A.Y.; Kurath, D.E.

    1996-04-01

    Approximately 61 million gallons of nuclear waste generated in plutonium production, radionuclide removal campaigns, and research and development activities is stored on the Department of Energy`s Hanford Site, near Richland, Washington. Although the pretreatment process and disposal requirements are still being defined, most pretreatment scenarios include removal of cesium from the aqueous streams. In many cases, after cesium is removed, the dissolved salt cakes and supernates can be disposed of as LLW. Ion exchange has been a leading candidate for this separation. Ion exchange systems have the advantage of simplicity of equipment and operation and provide many theoretical stages in a small space. The organic ion exchange material Duolite{trademark} CS-100 has been selected as the baseline exchanger for conceptual design of the Initial Pretreatment Module (IPM). Use of CS-100 was chosen because it is considered a conservative, technologically feasible approach. During FY 96, final resin down-selection will occur for IPM Title 1 design. Alternate ion exchange materials for cesium exchange will be considered at that time. The purpose of this report is to conduct a search for commercially available ion exchange materials which could potentially replace CS-100. This report will provide where possible a comparison of these resin in their ability to remove low concentrations of cesium from highly alkaline solutions. Materials which show promise can be studied further, while less encouraging resins can be eliminated from consideration.

  8. Influence of Ionic Liquids on the Selectivity of Ion Exchange-Based Polymer Membrane Sensing Layers.

    PubMed

    Mendecki, Lukasz; Callan, Nicole; Ahern, Meghan; Schazmann, Benjamin; Radu, Aleksandar

    2016-07-16

    The applicability of ion exchange membranes is mainly defined by their permselectivity towards specific ions. For instance, the needed selectivity can be sought by modifying some of the components required for the preparation of such membranes. In this study, a new class of materials -trihexyl(tetradecyl)phosphonium based ionic liquids (ILs) were used to modify the properties of ion exchange membranes. We determined selectivity coefficients for iodide as model ion utilizing six phosphonium-based ILs and compared the selectivity with two classical plasticizers. The dielectric properties of membranes plasticized with ionic liquids and their response characteristics towards ten different anions were investigated using potentiometric and impedance measurements. In this large set of data, deviations of obtained selectivity coefficients from the well-established Hofmeister series were observed on many occasions thus indicating a multitude of applications for these ion-exchanging systems.

  9. Influence of Ionic Liquids on the Selectivity of Ion Exchange-Based Polymer Membrane Sensing Layers

    PubMed Central

    Mendecki, Lukasz; Callan, Nicole; Ahern, Meghan; Schazmann, Benjamin; Radu, Aleksandar

    2016-01-01

    The applicability of ion exchange membranes is mainly defined by their permselectivity towards specific ions. For instance, the needed selectivity can be sought by modifying some of the components required for the preparation of such membranes. In this study, a new class of materials –trihexyl(tetradecyl)phosphonium based ionic liquids (ILs) were used to modify the properties of ion exchange membranes. We determined selectivity coefficients for iodide as model ion utilizing six phosphonium-based ILs and compared the selectivity with two classical plasticizers. The dielectric properties of membranes plasticized with ionic liquids and their response characteristics towards ten different anions were investigated using potentiometric and impedance measurements. In this large set of data, deviations of obtained selectivity coefficients from the well-established Hofmeister series were observed on many occasions thus indicating a multitude of applications for these ion-exchanging systems. PMID:27438837

  10. Equilibrium Model for Ion Exchange Between Multivalent Cations and Zeolite-A in a Molten Salt

    SciTech Connect

    Supathorn Phongikaroon; Michael Simpson

    2005-10-01

    A two-site equilibrium model that previously only accommodated monovalent cations has been extended to include divalent and trivalent cations for ion exchange between zeolite-A and molten chloride salts, a process being considered for concentrating nuclear fission products into high level waste forms. Equilibrium constants were determined by fitting the model to equilibrium data sets for ion exchange between zeolite-A and Cs ternary salt (CsCl-LiCl-KCl), Rb ternary salt (RbCl-LiCl-KCl), Na ternary salt (NaCl-LiCl-KCl), Sr ternary salt (SrCl2-LiCl-KCl), and U ternary salt (UCl3-LiCl-KCl). The results reveal a good fit between the experimental data sets and the model. The two ion exchange sites, framework sites and occluded sites, demonstrate different relative selectivities for the cations. It was found that Sr2_ is the preferred cation in the ion exchange site, and Cs_ is the preferred cation in the occlusion site. Meanwhile, Li_ has the highest combined selectivity when both ion exchange and occlusion sites are considered. Interestingly, divalent and trivalent species are more preferred in the ion exchange site than the monovalent species with the exception of Li_.

  11. Ion-exchange material and method of storing radioactive wastes

    DOEpatents

    Komarneni, S.; Roy, D.M.

    1983-10-31

    A new cation exchanger is a modified tobermorite containing aluminum isomorphously substituted for silicon and containing sodium or potassium. The exchanger is selective for lead, rubidium, cobalt, and cadmium and is selective for cesium over calcium or sodium. The tobermorites are compatible with cement and are useful for the long-term fixation and storage of radioactive nuclear wastes.

  12. Barcoded materials based on photoluminescent hybrid system of lanthanide ions-doped metal organic framework and silica via ion exchange.

    PubMed

    Shen, Xiang; Yan, Bing

    2016-04-15

    A multicolored photoluminescent hybrid system based on lanthanide ions-doped metal organic frameworks/silica composite host has potential in display and barcode applications. By controlling the stoichiometry of the lanthanides via cation exchange, proportional various lanthanide ions are successfully introduced into metal organic frameworks, whose emission intensity is correspondingly proportional to its amount. The resulting luminescent barcodes depend on the lanthanide ions ratios and compositions. Subsequently, the lanthanide ions located in the channels of metal organic frameworks are protected from any interaction with the environment after the modification of silica on the surface. The optical and thermal stability of the hybrid materials are improved for technological application.

  13. Estimating Soil Cation Exchange Capacity from Soil Physical and Chemical Properties

    NASA Astrophysics Data System (ADS)

    Bateni, S. M.; Emamgholizadeh, S.; Shahsavani, D.

    2014-12-01

    The soil Cation Exchange Capacity (CEC) is an important soil characteristic that has many applications in soil science and environmental studies. For example, CEC influences soil fertility by controlling the exchange of ions in the soil. Measurement of CEC is costly and difficult. Consequently, several studies attempted to obtain CEC from readily measurable soil physical and chemical properties such as soil pH, organic matter, soil texture, bulk density, and particle size distribution. These studies have often used multiple regression or artificial neural network models. Regression-based models cannot capture the intricate relationship between CEC and soil physical and chemical attributes and provide inaccurate CEC estimates. Although neural network models perform better than regression methods, they act like a black-box and cannot generate an explicit expression for retrieval of CEC from soil properties. In a departure with regression and neural network models, this study uses Genetic Expression Programming (GEP) and Multivariate Adaptive Regression Splines (MARS) to estimate CEC from easily measurable soil variables such as clay, pH, and OM. CEC estimates from GEP and MARS are compared with measurements at two field sites in Iran. Results show that GEP and MARS can estimate CEC accurately. Also, the MARS model performs slightly better than GEP. Finally, a sensitivity test indicates that organic matter and pH have respectively the least and the most significant impact on CEC.

  14. ROTARY FILTER FINES TESTING FOR SMALL COLUMN ION EXCHANGE

    SciTech Connect

    Herman, D.

    2011-08-03

    SRNL was requested to quantify the amount of 'fines passage' through the 0.5 micron membranes currently used for the rotary microfilter (RMF). Testing was also completed to determine if there is any additional benefit to utilizing a 0.1 micron filter to reduce the amount of fines that could pass through the filter. Quantifying of the amount of fines that passed through the two sets of membranes that were tested was accomplished by analyzing the filtrate by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES) for titanium. Even with preparations to isolate the titanium, all samples returned results of less than the instrument's detection limit of 0.184 mg/L. Test results show that the 0.5 micron filters produced a significantly higher flux while showing a negligible difference in filtrate clarity measured by turbidity. The first targeted deployment of the RMF is with the Small Column Ion Exchange (SCIX) at the Savannah River Site (SRS). SCIX uses crystalline silicotitanate (CST) to sorb cesium to decontaminate a clarified salt solution. The passage of fine particles through the filter membranes in sufficient quantities has the potential to impact the downstream facilities. To determine the amount of fines passage, a contract was established with SpinTek Filtration to operate a 3-disk pilot scale unit with prototypic filter disk and various feeds and two different filter disk membranes. SpinTek evaluated a set of the baseline 0.5 micron filter disks as well as a set of 0.1 micron filter disks to determine the amount of fine particles that would pass the membrane and to determine the flux each set produced. The membrane on both disk sets is manufactured by the Pall Corporation (PMM 050). Each set of disks was run with three feed combinations: prototypically ground CST, CST plus monosodium titanate (MST), and CST, MST, plus Sludge Batch 6 (SB6) simulant. Throughout the testing, samples of the filtrate were collected, measured for turbidity, and sent back

  15. CHARACTERIZATION OF CYCLED SPHERICAL RESORCINOL-FORMALDEHYDE ION EXCHANGE RESIN

    SciTech Connect

    Nash, C.; Duignan, M.

    2010-02-23

    This report presents characterization data for two spherical resorcinol-formaldehyde (sRF) resin beds that had processed cesium in non-radioactive and radioactive cycles. All column cycle operations for the resin beds including loading, displacements, elution, regeneration, breakthroughs, and solution analyses are reported in Nash and Duignan, 2009a. That report covered four ion exchange (IX) campaigns using the two {approx}11 mL beds in columns in a lead-lag arrangement. The first two campaigns used Savannah River Site (SRS) Tank 2F nonradioactive simulant while the latter two were fed with actual dissolved salt in the Savannah River National Laboratory (SRNL) Shielded Cells. Both radioactive cycles ran to cesium breakthrough of the lead column. The resin beds saw in excess of 400 bed volumes of feed in each cycle. Resin disposal plans in tank farm processing depend on characterizations of resin used with actual tank feed. Following a final 30 bed volume (BV) elution with nitric acid, the resin beds were found to contain detectable chromium, barium, boron, aluminum, iron, sodium, sulfur, plutonium, cesium, and mercury. Resin affinity for plutonium is important in criticality safety considerations. Cesium-137 was found to be less than 10E+7 dpm/g of resin, similar to past work with sRF resin. Sulfur levels are reasonably consistent with other work and are expected to represent sulfur chemistry used in the resin manufacture. There were low but detectable levels of technetium, americium, and curium. Toxicity Characteristic Leaching Procedure (TCLP) work on the used (eluted) resin samples showed significant contents of mercury, barium, and chromium. One resin sample exceeded the TCLP level for mercury while the other metals were below TCLP levels. TCLP organics measurements indicated measurable benzene in one case, though the source was unknown. Results of this work were compared with other work on similar sRF resin characterizations in this report. This is the first

  16. Neutral atomic oxygen beam produced by ion charge exchange for Low Earth Orbital (LEO) simulation

    NASA Technical Reports Server (NTRS)

    Banks, Bruce; Rutledge, Sharon; Brdar, Marko; Olen, Carl; Stidham, Curt

    1987-01-01

    A low energy neutral atomic oxygen beam system was designed and is currently being assembled at the Lewis Research Center. The system utilizes a 15 cm diameter Kaufman ion source to produce positive oxygen ions which are charge exchange neutralized to produce low energy (variable from 5 to 150 eV) oxygen atoms at a flux simulating real time low Earth orbital conditions. An electromagnet is used to direct only the singly charged oxygen ions from the ion source into the charge exchange cell. A retarding potential grid is used to slow down the oxygen ions to desired energies prior to their charge exchange. Cryogenically cooled diatomic oxygen gas in the charge exchange cell is then used to transfer charge to the oxygen ions to produce a neutral atomic oxygen beam. Remaining non-charge exchanged oxygen ions are then swept from the beam by electromagnetic or electrostatic deflection depending upon the desired experiment configuration. The resulting neutral oxygen beam of 5 to 10 cm in diameter impinges upon target materials within a sample holder fixture that can also provide for simultaneous heating and UV exposure during the atomic oxygen bombardment.

  17. Studying ion exchange in solution and at biological membranes by FCS.

    PubMed

    Widengren, Jerker

    2013-01-01

    By FCS, a wide range of processes can be studied, covering time ranges from subnanoseconds to seconds. In principle, any process at equilibrium conditions can be measured, which reflects itself by a change in the detected fluorescence intensity. In this review, it is described how FCS and variants thereof can be used to monitor ion exchange, in solution and along biological membranes. Analyzing fluorescence fluctuations of ion-sensitive fluorophores by FCS offers selective advantages over other techniques for measuring local ion concentrations, and, in particular, for studying exchange kinetics of ions on a very local scale. This opens for several areas of application. The FCS approach was used to investigate fundamental aspects of proton exchange at and along biological membranes. The protonation relaxation rate, as measured by FCS for a pH-sensitive dye, can also provide information about local accessibility/interaction of a particular labeling site and conformational states of biomolecules, in a similar fashion as in a fluorescence quenching experiment. The same FCS concept can also be applied to ion exchange studies using other ion-sensitive fluorophores, and by use of dyes sensitive to other ambient conditions the concept can be extended also beyond ion exchange studies.

  18. Intensification of ammonia removal from waste water in biologically active zeolitic ion exchange columns.

    PubMed

    Almutairi, Azel; Weatherley, Laurence R

    2015-09-01

    The use of nitrification filters for the removal of ammonium ion from waste-water is an established technology deployed extensively in municipal water treatment, in industrial water treatment and in applications such as fish farming. The process involves the development of immobilized bacterial films on a solid packing support, which is designed to provide a suitable host for the film, and allow supply of oxygen to promote aerobic action. Removal of ammonia and nitrite is increasingly necessary to meet drinking water and discharge standards being applied in the US, Europe and other places. Ion-exchange techniques are also effective for removal of ammonia (as the ammonium ion) from waste water and have the advantage of fast start-up times compared to biological filtration which in some cases may take several weeks to be fully operational. Here we explore the performance of ion exchange columns in which nitrifying bacteria are cultivated, with the goal of a "combined" process involving simultaneous ion-exchange and nitrification, intensified by in-situ aeration with a novel membrane module. There were three experimental goals. Firstly, ion exchange zeolites were characterized and prepared for comparative column breakthrough studies for ammonia removal. Secondly effective in-situ aeration for promotion of nitrifying bacterial growth was studied using a number of different membranes including polyethersulfone (PES), polypropylene (PP), nylon, and polytetra-fluoroethylene (PTFE). Thirdly the breakthrough performance of ion exchange columns filled with zeolite in the presence of aeration and in the presence of nitrifying bacteria was determined to establish the influence of biomass, and aeration upon breakthrough during ammonium ion uptake. The methodology adopted included screening of two types of the naturally occuring zeolite clinoptilolite for effective ammonia removal in continuous ion-exchange columns. Next, the performance of fixed beds of clinoptilolite in the

  19. Development of a transparent, non-cytotoxic, silver ion-exchanged glass with antimicrobial activity and low ion elution.

    PubMed

    Shim, Gyu-In; Kim, Seong-Hwan; Eom, Hyung-Woo; Kim, Kwang-Mahn; Choi, Se-Young

    2015-05-01

    We investigated the antimicrobial, cytotoxicity, skin irritation, and ion elution behaviors of glass doped with silver ions with respect to its application to electronic equipment such as phones and tablet screens. The microbes tested were Escherichia coli, Staphylococcus aureus, and Penicillium funiculosum. AgNO3 powder was spread on both sides of aluminosilicate glass, and it was heated to 250-280°C for 10min. Under optimized heating conditions (260°C, 10min), the antimicrobial activity of ion-exchanged glass against bacteria and fungi was over 99.9% after 24 weeks. The glass failed to irritate the skin of experimental animals and was considered non-cytotoxic. The maximum amount of Ag ions that were eluted from the ion-exchanged glass into drinking water was measured at 0.037±0.003μgL(-1), an amount which is several orders of magnitude below the standard limit of 0.1mgL(-1) in drinking water. Ag ion-exchanged glass had characteristics suitable for use as a display screen, such as a light transmittance of 90% and a surface roughness of 0.704nm. Our findings suggest that glass doped with silver ions is more hygienic than non-doped glass is, and should be applied to display screens and glassware.

  20. Adsorbents/ion exchangers-PVA blend membranes: Preparation, characterization and performance for the removal of Zn2+ by electrodialysis

    NASA Astrophysics Data System (ADS)

    Caprarescu, Simona; Radu, Anita-Laura; Purcar, Violeta; Ianchis, Raluca; Sarbu, Andrei; Ghiurea, Marius; Nicolae, Cristian; Modrogan, Cristina; Vaireanu, Danut-Ionel; Périchaud, Alain; Ebrasu, Daniela-Ion

    2015-02-01

    The present paper was aimed at studying the possibility of zinc (Zn) removal from the wastewater discharged from zinc electroplating processes. In order to save industrial and environmental resources, the concentrated solution could be reused after electrodialysis process. A mini-electrodialysis system with three cylindrical compartments and different membranes containing various resins (Purolite A500 and Hypersol-Macronet MN500) was employed, which can be further applied for the treatment of synthetic effluent which contained zinc ions. The electrodialysis system was operated at constant voltage using different concentrations of synthetic solutions of zinc ions, without and with electrolyte recirculation for 1.5 h. The pH and conductivity of solutions were measured before and after the electrodialysis process occurs. Also the removal ratio (Rr) and mass flow (J) of zinc ions, energy consumption (EC) and current efficiency (CE) were determined. It was found that electrodialysis treatment generated a very low conductivity solution, enabling its reuse as rinse water. According to the obtained results when using a membrane pair with higher ion exchange capacity (IEC) the removal ratio is improved (over 80%). The physico-chemical, structural and mechanical properties of prepared membranes were registered, before and after electrodialysis process takes place, by means of complementary analytical techniques, namely, ion-exchange capacity, water content and thickness measurements. Furthermore analysis were also carried out by Fourier transform infrared spectroscopy (FT-IR), environmental scanning electron microscopy (ESEM), thermal gravimetric analysis (TGA) and electrochemical impedance spectroscopy (EIS).

  1. Influence of ion bombardment induced patterning of exchange bias in pinned artificial ferrimagnets on the interlayer exchange coupling

    SciTech Connect

    Hoeink, V.; Schmalhorst, J.; Reiss, G.; Weis, T.; Lengemann, D.; Engel, D.; Ehresmann, A.

    2008-06-15

    Artificial ferrimagnets have many applications as, e.g., pinned reference electrodes in magnetic tunnel junctions. It is known that the application of ion bombardment (IB) induced patterning of the exchange bias coupling of a single layer reference electrode in magnetic tunnel junctions with He ions is possible. For applications as, e.g., special types of magnetic logic, a combination of the IB induced patterning of the exchange bias coupling and the implementation of an artificial ferrimagnet as reference electrode is desirable. Here, investigations for a pinned artificial ferrimagnet with a Ru interlayer, which is frequently used in magnetic tunnel junctions, are presented. It is shown that in this kind of samples the exchange bias can be increased or rotated by IB induced magnetic patterning with 10 keV He ions without a destruction of the antiferromagnetic interlayer exchange coupling. An IrMn/Py/Co/Cu/Co stack turned out to be more sensitive to the influence of IB than the Ru based artificial ferrimagnet.

  2. An Integrated Chemical Reactor-Heat Exchanger Based on Ammonium Carbamate (POSTPRINT)

    DTIC Science & Technology

    2012-10-01

    display, or disclose the work. 14. ABSTRACT In this work we present our recent effort in developing a novel heat exchanger based on endothermic ...conditions. 15. SUBJECT TERMS aircraft thermal management, ammonium carbamate, chemical reactor heat exchanger, endothermic decomposition 16... endothermic chemical reaction (HEX reactor). The proposed HEX reactor is designed to provide additional heat sink capability for aircraft thermal management

  3. Quantifying exchange coupling in f-ion pairs using the diamagnetic substitution method

    SciTech Connect

    Lukens, Wayne W.; Walter, Marc D.

    2010-04-01

    One of the challenges in the chemistry of actinide and lanthanide (f-ion) is quantifying exchange coupling between f-ions. While qualitative information about exchange coupling may be readily obtained using the diamagnetic substitution approach, obtaining quantitative information is much more difficult. This article describes how exchange coupling may be quantified using the susceptibility of a magnetically isolated analog, as in the diamagnetic substitution approach, along with the anisotropy of the ground state as determined by EPR spectroscopy. Several examples are used to illustrate and test this approach.

  4. Quantifying exchange coupling in f-ion pairs using the diamagnetic substitution method.

    PubMed

    Lukens, Wayne W; Walter, Marc D

    2010-05-17

    One of the challenges in the chemistry of actinide and lanthanide (f-ion) complexes is quantifying exchange coupling of f-ions. While qualitative information about exchange coupling may be readily obtained using the diamagnetic substitution approach, obtaining quantitative information is much more difficult. This article describes how exchange coupling may be quantified using the susceptibility of a magnetically isolated analog, as in the diamagnetic substitution approach, along with the anisotropy of the ground state, as determined by EPR spectroscopy. Several examples are used to illustrate and test this approach.

  5. Donnan dialysis of transition metal ions using anion exchange membrane modified with Xylenol Orange

    SciTech Connect

    Sawicka, B.; Brajter, K.; Trojanowicz, M.; Kado, B. )

    1991-01-01

    A chelating ion-exchange membrane was obtained by modification of a PTFE-based anion-exchange membrane with Xylenol Orange. Its utility for dialysis of Cu(II), Ni(II), Mn(II), and Zn(II) was investigated by using receiver solutions without and with iminodiacetate. 1,2-diaminocyclohexanetetraacetic acid, and tetraethylenepentamine. In comparison to commercial PTFE cation-exchange membranes, modified chelating membranes exhibit for the metal ions investigated a larger differentiation of retention in the membrane phase and transport-to-receiver solution depending on the modifier used and the composition of the receiver solution.

  6. Chemical damage and aging of ion bombarded PPS

    NASA Astrophysics Data System (ADS)

    Rizzatti, M. R.; de Araújo, M. A.; Livi, R. P.

    2000-09-01

    Thin foils of commercial grade polyphenylene sulfide (PPS), 2 μm thick, were bombarded with energetic H + (300 keV), He + (350 keV), B + (350 keV) and Ar ++ (700 keV) ions at fluences ranging from 10 12 to 10 15 ions/cm2. Fourier transform infrared spectroscopy (FTIR), Rutherford backscattering analysis (RBS) and chemical elemental analysis (CHN) were performed to evaluate the chemical changes induced by ion bombardment in the polymeric samples. It was verified that the S-S and C-S acyclic bonds were more susceptible to ion bombardment, and the aromatic ring bonds are the most resistant ones. The effective modification radii for the bond breaking and recombination processes were extracted. The aging of bombarded PPS was monitored and oxygen and nitrogen uptake increased linearly with time.

  7. Metal-air cell with ion exchange material

    DOEpatents

    Friesen, Cody A.; Wolfe, Derek; Johnson, Paul Bryan

    2015-08-25

    Embodiments of the invention are related to anion exchange membranes used in electrochemical metal-air cells in which the membranes function as the electrolyte material, or are used in conjunction with electrolytes such as ionic liquid electrolytes.

  8. Study of plasma off-gas treatment from spent ion exchange resin pyrolysis.

    PubMed

    Castro, Hernán Ariel; Luca, Vittorio; Banchi, Hugo Luis

    2017-03-23

    Polystyrene divinylbenzene-based ion exchange resins are employed extensively within nuclear power plants (NPPs) and research reactors for purification and chemical control of the cooling water system. To maintain the highest possible water quality, the resins are regularly replaced as they become contaminated with a range of isotopes derived from compromised fuel elements as well as corrosion and activation products including (14)C, (60)Co, (90)Sr, (129)I, and (137)Cs. Such spent resins constitute a major proportion (in volume terms) of the solid radioactive waste generated by the nuclear industry. Several treatment and conditioning techniques have been developed with a view toward reducing the spent resin volume and generating a stable waste product suitable for long-term storage and disposal. Between them, pyrolysis emerges as an attractive option. Previous work of our group suggests that the pyrolysis treatment of the resins at low temperatures between 300 and 350 °C resulted in a stable waste product with a significant volume reduction (>50%) and characteristics suitable for long-term storage and/or disposal. However, another important issue to take into account is the complexity of the off-gas generated during the process and the different technical alternatives for its conditioning. Ongoing work addresses the characterization of the ion exchange resin treatment's off-gas. Additionally, the application of plasma technology for the treatment of the off-gas current was studied as an alternative to more conventional processes utilizing oil- or gas-fired post-combustion chambers operating at temperatures in excess of 1000 °C. A laboratory-scale flow reactor, using inductively coupled plasma, operating under sub-atmospheric conditions was developed. Fundamental experiments using model compounds have been performed, demonstrating a high destruction and removal ratio (>99.99%) for different reaction media, at low reactor temperatures and moderate power

  9. Separation of hemicellulose-derived saccharides from wood hydrolysate by lime and ion exchange resin.

    PubMed

    Wang, Xiaojun; Zhuang, Jingshun; Fu, Yingjuan; Tian, Guoyu; Wang, Zhaojiang; Qin, Menghua

    2016-04-01

    A combined process of lime treatment and mixed bed ion exchange was proposed to separate hemicellulose-derived saccharides (HDS) from prehydrolysis liquor (PHL) of lignocellulose as value added products. The optimization of lime treatment achieved up to 44.2% removal of non-saccharide organic compounds (NSOC), mainly colloidal substances, with negligible HDS degradation at 0.5% lime level and subsequent neutralization by phosphoric acid. The residual NSOC and calcium ions in lime-treated PHL were eliminated by mixed bed ion exchange. The breakthrough curves of HDS and NSOC showed selective retention toward NSOC, leading to 75% HDS recovery with 95% purity at 17 bed volumes of exchange capacity. In addition, macroporous resin showed higher exchange capacity than gel resin as indicated by the triple processing volume. The remarkable selectivity of the combined process suggested the feasibility for HDS separation from PHL.

  10. Evolution of ion-exchange: from Moses to the Manhattan Project to modern times.

    PubMed

    Lucy, Charles A

    2003-06-06

    This article explores the history of ion-exchange from records of desalination in the Old Testament and the writings of Aristotle, to the identification of the phenomenon of ion-exchange by two English agricultural chemists, to the invention of suppressed conductivity by Small et al. [Anal. Chem. 54 (1975) 462]. It then focuses on the characteristics of the gradual and continuous evolution of ion chromatography with suppressed conductivity to its current state, with an emphasis on those discoveries that punctuated or revolutionized this evolution.

  11. CoMOR zeolite catalyst prepared by buffered ion exchange for effective decomposition of nitrous oxide.

    PubMed

    Zhang, Xinyan; Shen, Qun; He, Chi; Wang, Yufei; Cheng, Jie; Hao, Zhengping

    2011-09-15

    Co contained MOR zeolite catalysts with high Co loadings were successfully synthesized by buffered ion exchange at pH 8, and were tested for N(2)O catalytic decomposition. The high exchange level of synthesized CoMOR(x)-BIE catalysts probably benefits from the maximizing hydroxycomplexes Co(OH)(+) ion in the buffered solution, which is more preferred for the ion exchange with the zeolites. It has been found that the novel CoMOR(x)-BIE catalysts exhibit excellent catalytic activities, which is attributed to the large population of isolated Co(2+) ions on ion exchange positions. The most active CoMOR(130)-BIE catalyst shows high resistance to the inhibition of oxygen, NO and water vapor. Furthermore, stability tests indicate that the CoMOR(130)-BIE catalyst has no obvious deactivation under simulated emission conditions after reaction for more than 100 h. This extraordinary durability could be related to its high Co(2+) content and low Brönsted acidity sites in the catalyst, which facilitate the stability of active isolated Co(2+) on ion exchange positions. Thus, the CoMOR(130)-BIE catalyst shows a great potential as a cost-effective catalyst for N(2)O elimination in future applications.

  12. Management of Spent Organic Ion-Exchange Resins by Photochemical Oxidation

    SciTech Connect

    Srinivas, C.; Sugilal, S.; Wattal, P. K.

    2003-02-26

    Management of spent ion-exchange resin waste arising from nuclear reactor operations by traditional practice of encapsulation in cement is associated with problems such as swelling and disintegration. Complete oxidation (mineralization) is an attractive alternative option. This paper reports the development of photochemical mineralization process for organic ion-exchange resins of poly (styrene-divinyl benzene) type with sulfonic acid and quaternary ammonium functional groups. It is a two-step process consisting of dissolution (conversion of solid resin into water-soluble reaction products) and photo-Fenton mineralization of the dissolved resin. Cation and anion resin dissolution was effected by reaction of the resin with H2O2 at 50-60 C in the presence of ferrous/copper sulphate catalyst. Direct dissolution of mixed resin was not efficient. However, the cation resin portion in the mixed resin could be selectively dissolved without affecting the anion portion. The solid anion resin after separation from the cation resin solution could be dissolved. About 0.5 liters of 50% H2O2 was required for dissolution of one kg of wet resin. The reaction time was 4-5 hours. Dissolution experiments were conducted on up to 8 liters of wet resin. The second step, viz., photo-Fenton mineralization of the dissolved resin was effected at ambient temperature(25-35 C). Kinetic results of laboratory scale experiments in immersion type photo-reactor and pilot scale experiments in tubular flow photo-reactor were presented. These results clearly demonstrated the photo-Fenton mineralization of dissolved resin at ambient temperature with stoichiometric quantity of H2O2 as against 70-200% excess H2O2 requirement in chemical mineralization experiments under Fenton oxidation conditions at 90-95 C. Based on these studies, a treatment scheme was developed and presented in this paper.

  13. Active membrane having uniform physico-chemically functionalized ion channels

    DOEpatents

    Gerald, II, Rex E; Ruscic, Katarina J; Sears, Devin N; Smith, Luis J; Klingler, Robert J; Rathke, Jerome W

    2012-09-24

    The present invention relates to a physicochemically-active porous membrane for electrochemical cells that purports dual functions: an electronic insulator (separator) and a unidirectional ion-transporter (electrolyte). The electrochemical cell membrane is activated for the transport of ions by contiguous ion coordination sites on the interior two-dimensional surfaces of the trans-membrane unidirectional pores. One dimension of the pore surface has a macroscopic length (1 nm-1000 .mu.m) and is directed parallel to the direction of an electric field, which is produced between the cathode and the anode electrodes of an electrochemical cell. The membrane material is designed to have physicochemical interaction with ions. Control of the extent of the interactions between the ions and the interior pore walls of the membrane and other materials, chemicals, or structures contained within the pores provides adjustability of the ionic conductivity of the membrane.

  14. Chemically assisted ion beam etching of polycrystalline and (100)tungsten

    NASA Technical Reports Server (NTRS)

    Garner, Charles

    1987-01-01

    A chemically assisted ion-beam etching technique is described which employs an ion beam from an electron-bombardment ion source and a directed flux of ClF3 neutrals. This technique enables the etching of tungsten foils and films in excess of 40 microns thick with good anisotropy and pattern definition over areas of 30 sq mm, and with a high degree of selectivity. (100) tungsten foils etched with this process exhibit preferred-orientation etching, while polycrystalline tungsten films exhibit high etch rates. This technique can be used to pattern the dispenser cathode surfaces serving as electron emitters in traveling-wave tubes to a controlled porosity.

  15. Automated resource-saving technology of ion-exchange water treatment

    NASA Astrophysics Data System (ADS)

    Livshits, M.

    2015-01-01

    Stable high quality of the purified water can be provided by adaptive control of water-treatment installations with the observer in a loop of the control system on the basis of observer of ion exchange processes. To obtain this goal the following problems have been solved: the hierarchic structure of water treatment system is developed; the system of water treatment quality criteria for ion exchange processes is developed; the created mathematical model of ionic exchange processes is functionally oriented to application in control system as an observer; methodologies of identification of a mathematical model of ionic exchange processes is developed; verification of the mathematical model of ionic exchange is performed on experimental-industrial basis; automatic control system of water treatment with observer in the loop is developed for low-waste installation of a heat supply system.

  16. Novel ion-exchange membranes for electrodialysis prepared by radiation-induced graft polymerization

    SciTech Connect

    Tsuneda, Satoshi; Saito, Kyoichi; Misuhara, Hisashi; Sugo, Takanobu

    1995-11-01

    Ion-exchange membranes have been used to concentrate seawater to produce salt as well as to desalinate brackish water to render it potable. Also, the interest in applications of ion-exchange membranes as separators for electrodialytic desalination of bioproducts and separators in hydrogen-oxygen fuel cells has been growing. Novel ion-exchange membranes containing sulfonic acid (SO{sub 3}H) and trimethyl ammonium [N(CH{sub 3}){sub 3}] groups were prepared by a simple method of radiation-induced cografting of sodium styrene sulfonate (SSS) with acrylic acid (AAc) and vinyl benzyl trimethyl ammonium chloride (VBTAC) with 2-hydroxyethyl methacrylate (HEMA), onto a polyethylene film with a thickness of 50 {micro}m. The high density graft chain was introduced throughout the polyethylene film. The maximum cation- and anion-exchange capacities of the resultant membranes were 2.5 and 1.3 mol/kg, receptively. These membranes exhibited an electrical resistance one order lower than commercially available ion-exchange membranes; for example, 12 h cografting provided cation- and anion-exchange membranes whose electrical resistances in a 0.5 M NaCl solution were 0.25 and 0.85 {Omega} cm{sup 2}, respectively. From the evaluation of electrodialytic desalination in a batch mode, using a pair of the graft-type ion-exchange membranes, the time required to achieve 99.5% desalination of the initial 0.5 M NaCl solutions was reduced to 85% comparing with that of the commercial ion-exchange membranes.

  17. Ion temperatures in HIP-1 and SUMMA from charge-exchange neutral optical emission spectra

    NASA Technical Reports Server (NTRS)

    Patch, R. W.; Lauver, M. R.

    1976-01-01

    Ion temperatures were obtained from observations of the H sub alpha, D sub alpha, and He 587.6 nm lines emitted from hydrogen, deuterium, and helium plasmas in the SUMMA and HIP-1 mirror devices at Lewis Research Center. Steady state discharges were formed by applying a radially inward dc electric field between cylindrical or annular anodes and hollow cathodes located at the peaks of the mirrors. The ion temperatures were found from the Doppler broadening of the charge-exchange components of spectral lines. A statistical method was developed for obtaining scaling relations of ion temperature as a function of current, voltage, and magnetic flux density. Derivations are given that take into account triangular monochromator slit functions, loss cones, and superimposed charge-exchange processes. In addition, the Doppler broadening was found to be sensitive to the influence of drift on charge-exchange cross section. The effects of finite ion-cyclotron radius, cascading, and delayed emission are reviewed.

  18. Biocompatibility Research of a Novel pH Sensitive Ion Exchange Resin Microsphere

    PubMed Central

    Liu, Hongfei; Shi, Shuangshuang; Pan, Weisan; Sun, Changshan; Zou, Xiaomian; Fu, Min; Feng, Yingshu; Ding, Hui

    2014-01-01

    The main objective of this study was to investigate biocompatibility and provide in-vivo pharmacological and toxicological evidence for further investigation of the possibility of pH sensitive ion exchange resin microsphere for clinical utilizations. Acute toxicity study and general pharmacological studies were conducted on the pH sensitive ion exchange resin microsphere we prepared. The general pharmacological studies consist of the effects of the pH sensitive ion exchange resin microsphere on the nervous system of mice, the functional coordination of mice, the hypnosis of mice treated with nembutal at subliminal dose, the autonomic activities of tested mice, and the heart rate, blood pressure, ECG and breathing of the anesthetic cats. The LD50 of pH sensitive ion exchange resin microsphere after oral administration was more than 18.84 g·Kg-1. Mice were orally administered with 16 mg·Kg-1, 32 mg·Kg-1 and 64 mg·Kg-1 of pH sensitive ion exchange resin microsphere and there was no significant influence on mice nervous system, general behavior, function coordination, hypnotic effect treated with nembutal at subliminal dose and frequency of autonomic activities. Within the 90 min after 5 mg·Kg-1, 10 mg·Kg-1, 20 mg·Kg-1 pH sensitive ion exchange resin microsphere was injected to cat duodenum, the heart rate, blood pressure, breathing and ECG of the cats didn’t make significant changes in each experimental group compared with the control group. The desirable pharmacological and toxicological behaviors of the pH sensitive ion exchange resin microsphere exhibited that it has safe biocompatibility and is possible for clinical use. PMID:25276183

  19. Biocompatibility Research of a Novel pH Sensitive Ion Exchange Resin Microsphere.

    PubMed

    Liu, Hongfei; Shi, Shuangshuang; Pan, Weisan; Sun, Changshan; Zou, Xiaomian; Fu, Min; Feng, Yingshu; Ding, Hui

    2014-01-01

    The main objective of this study was to investigate biocompatibility and provide in-vivo pharmacological and toxicological evidence for further investigation of the possibility of pH sensitive ion exchange resin microsphere for clinical utilizations. Acute toxicity study and general pharmacological studies were conducted on the pH sensitive ion exchange resin microsphere we prepared. The general pharmacological studies consist of the effects of the pH sensitive ion exchange resin microsphere on the nervous system of mice, the functional coordination of mice, the hypnosis of mice treated with nembutal at subliminal dose, the autonomic activities of tested mice, and the heart rate, blood pressure, ECG and breathing of the anesthetic cats. The LD50 of pH sensitive ion exchange resin microsphere after oral administration was more than 18.84 g·Kg(-1). Mice were orally administered with 16 mg·Kg(-1), 32 mg·Kg(-1) and 64 mg·Kg(-1) of pH sensitive ion exchange resin microsphere and there was no significant influence on mice nervous system, general behavior, function coordination, hypnotic effect treated with nembutal at subliminal dose and frequency of autonomic activities. Within the 90 min after 5 mg·Kg(-1), 10 mg·Kg(-1), 20 mg·Kg(-1) pH sensitive ion exchange resin microsphere was injected to cat duodenum, the heart rate, blood pressure, breathing and ECG of the cats didn't make significant changes in each experimental group compared with the control group. The desirable pharmacological and toxicological behaviors of the pH sensitive ion exchange resin microsphere exhibited that it has safe biocompatibility and is possible for clinical use.

  20. Proton Exchange in a Paramagnetic Chemical Exchange Saturation Transfer Agent from Experimental Studies and ab Initio Metadynamics Simulation.

    PubMed

    Pollet, Rodolphe; Bonnet, Célia S; Retailleau, Pascal; Durand, Philippe; Tóth, Éva

    2017-03-27

    The proton-exchange process between water and a carbamate has been studied experimentally and theoretically in a lanthanide-based paramagnetic chemical exchange saturation transfer agent endowed with potential multimodality detection capabilities (optical imaging, or T1 MRI for the Gd(III) analogue). In addition to an in-depth structural analysis by a combined approach (using X-ray crystallography, NMR, and molecular dynamics), our ab initio simulation in aqueous solution sheds light on the reaction mechanism for this proton exchange, which involves structural Grotthuss diffusion.

  1. Central metal ion exchange in a coordination polymer based on lanthanide ions and di(2-ethylhexyl)phosphoric acid: exchange rate and tunable affinity.

    PubMed

    Tasaki-Handa, Yuiko; Abe, Yukie; Ooi, Kenta; Tanaka, Mikiya; Wakisaka, Akihiro

    2014-01-01

    In this paper the exchange of lanthanide(III) ions (Ln(3+)) between a solution and a coordination polymer (CP) of di(2-ethylhexyl)phosphoric acid (Hdehp), [Ln(dehp)3], is studied. Kinetic and selectivity studies suggest that a polymeric network of [Ln(dehp)3] has different characteristics than the corresponding monomeric complex. The reaction rate is remarkably slow and requires over 600 h to reach in nearly equilibrium, and this can be explained by the polymeric crystalline structure and high valency of Ln(3+). The affinity of the exchange reaction reaches a maximum with the Ln(3+) possessing an ionic radius 7% smaller than that of the central Ln(3+), therefore, the affinity of the [Ln(dehp)3] is tunable based on the choice of the central metal ion. Such unique affinity, which differs from the monomeric complex, can be explained by two factors: the coordination preference and steric strain caused by the polymeric structure. The latter likely becomes predominant for Ln(3+) exchange when the ionic radius of the ion in solution is smaller than the original Ln(3+) by more than 7%. Structural studies suggest that the incoming Ln(3+) forms a new phase though an exchange reaction, and this could plausibly cause the structural strain.

  2. Local charge exchange of He+ ions at Aluminum surfaces

    NASA Astrophysics Data System (ADS)

    Riccardi, P.; Sindona, A.; Dukes, C. A.

    2017-04-01

    We report on experiments designed to observe the correlation between the autoionization of doubly excited helium atoms and the Auger decay of 2p vacancies in Al. The autoionizing states are formed when incident He+* and He++ are neutralized by resonant electron capture at the surface. 2p excitation in Al occurs in dielectronic charge transfer during the close encounter of an excited helium ion and an Al atom. These results clarify the mechanism for Al-2p excitation in the case of singly charged ground state He+(1s) ion impact, where the dielectronic transition occurs after promotion of the 1s electron of incoming ions.

  3. Selective separation of sodium ions from a mixture with phenylalanine by Donnan dialysis with a profiled sulfogroup cation exchange membrane

    NASA Astrophysics Data System (ADS)

    Vasil'eva, V. I.; Goleva, E. A.

    2013-11-01

    The possibility of separating ions of metal from a mixture with ampholyte (an amino acid) by Donnan dialysis with an MK-40 sulfogroup cation exchange membrane is demonstrated. Conditions ensuring the selectivity and intensity of the mass transfer of sodium ions from a mixture with bipolar phenylalanine ions into a diffusate containing hydrochloric acid through a cation exchange membrane are found.

  4. Integrated separation scheme for coal-derived liquids using ion-exchange and adsorption chromatography

    SciTech Connect

    Strachan, M.G.; Johns, R.B.

    1986-02-01

    A separation scheme for coal-derived liquids has been developed that separates by functionality into discrete compound classes using ion-exchange resins; neutrals are further subdivided into fractions differing in polarity, structure, and molecular weight by adsorption chromatography. Sufficient material can be separated to allow further characterization at both gross structural and molecular levels. It gives excellent overall reproducibility (+/- 4%) and recovery (>97%). Removal of acidic and base species prior to recovery of the liquefaction solvent by distillation is a major advantage of the method because it leads to a reduction both in the loss of lower boiling components and in the potential thermal alteration of the sample. The selectivity and discrimination of the procedure are demonstrated for a Victorian brown coal (Loy Yang field) liquefaction product as shown by spectroscopic and chemical analyses of its major fractions. The use of this method as a chemical probe can facilitate investigation of liquefaction mechanisms by enabling a ready selection for analysis of components varying according to a choice of parameters encompassing functionality, polarity, and structure. 29 references, 7 figures, 5 tables.

  5. Optimizing liquid waste treatment processing in PWRs: focus on modeling of the variation of ion-exchange resins selectivity coefficients

    SciTech Connect

    Gressier, Frederic; Van der Lee, Jan; Schneider, Helene; Bachet, Martin; Catalette, Hubert

    2007-07-01

    A bibliographic survey has highlighted the essential role of selectivity on resin efficiency, especially the variation of selectivity coefficients in function of the resin saturation state and the operating conditions. This phenomenon has been experimentally confirmed but is not yet implemented into an ion-exchange model specific for resins. This paper reviews the state of the art in predicting sorption capacity of ion-exchange resins. Different models accounting for ions activities inside the resin phase are available. Moreover, a comparison between the values found in the literature and our results has been done. The results of sorption experiments of cobalt chloride on a strong cationic gel type resin used in French PWRs are presented. The graph describing the variation of selectivity coefficient with respect to cobalt equivalent fraction is drawn. The parameters determined by the analysis of this graph are injected in a new physico-chemical law. Implementation of this model in the chemical speciation simulation code CHESS enables to study the overall effect of this approach for the sorption in a batch. (authors)

  6. Multi-angle ratiometric approach to measure chemical exchange in amide proton transfer imaging.

    PubMed

    Zu, Zhongliang; Janve, Vaibhav A; Li, Ke; Does, Mark D; Gore, John C; Gochberg, Daniel F

    2012-09-01

    Amide proton transfer imaging, a specific form of chemical exchange saturation transfer imaging, has previously been applied to studies of acute ischemic acidosis, stroke, and cancer. However, interpreting the resulting contrast is complicated by its dependence on the exchange rate between amides and water, the amide concentration, amide and water relaxation, and macromolecular magnetization transfer. Hence, conventional chemical exchange saturation transfer contrast is not specific to changes such as reductions in pH due to tissue acidosis. In this article, a multi-angle ratiometric approach based on several pulsed-chemical exchange saturation transfer scans at different irradiation flip angles is proposed to specifically reflect exchange rates only. This separation of exchange effects in pulsed-chemical exchange saturation transfer experiments is based on isolating rotation vs. saturation contributions, and such methods form a new subclass of chemical exchange rotation transfer (CERT) experiments. Simulations and measurements of creatine/agar phantoms indicate that a newly proposed imaging metric isolates the effects of exchange rate changes, independent of other sample parameters.

  7. Ion exchange determines iodine-131 concentration in aqueous samples

    NASA Technical Reports Server (NTRS)

    Fairman, W. D.; Sedlet, J.

    1967-01-01

    Inorganic radioiodide in aqueous media is analyzed by separating the radioactive iodine-131 as the iodide ion on a silver chloride column. The activity in the final precipitate may be determined by beta or gamma counting.

  8. PILOT-SCALE HYDRAULIC TESTING OF RESORCINOL FORMALDEHYDE ION EXCHANGE RESIN

    SciTech Connect

    Adamson, D.

    2009-05-28

    Savannah River National Laboratory (SRNL) performed pilot-scale hydraulic/chemical testing of spherical resorcinol formaldehyde (RF) ion exchange (IX) resin for the River Protection Project-Hanford Tank Waste Treatment & Immobilization Plant (WTP) Project. The RF resin hydraulic cycle testing was conducted in two pilot-scale IX columns, 1/4 and 1/2 scale. A total of twenty-three hydraulic/chemical cycles were successfully completed on the spherical RF resin. Sixteen of these cycles were completed in the 24-inch IX Column (1/2 scale column). Hydraulic testing showed that the permeability of the RF resin remained essentially constant, with no observed trend in the reduction of the permeability as the number of cycles increased. The permeability during the pilot-scale testing was 3 times better than the design requirements of the WTP full-scale IX system. The RF resin bed showed no tendency to form fissures or pack more densely as the number of cycles increased. Particle size measurements of the RF resin showed no indication of particle size change (for a given chemical) with cycles and essentially no fines formation. The permeability of the resin bed was uniform with respect to changes in bed depth. Upflow Regeneration and Simulant Introduction in the IX columns revealed another RF resin benefit; negligible radial pressures to the column walls from the swelling of resin beads. The hydraulic and chemical performance of the spherical RF resin during cycle testing was found to be superior to all other tested IX resins. The pilot-scale testing indicates that the RF resin is durable and should hold up to many hydraulic cycles in actual radioactive Cesium (Cs) separation.

  9. Comparison or organic and inorganic ion exchange materials for removal of cesium and strontium from Hanford waste

    SciTech Connect

    Brown, G.N.; Carson, K.J.; DesChane, J.R.; Elovich, R.J.

    1997-10-01

    This work is part of an ESP-CP task to develop and evaluate high-capacity, selective, solid extractants for the uptake of cesium, strontium, and technetium (Cs, Sr, and Tc) from nuclear wastes. Pacific Northwest National Laboratory (PNNL) staff, in collaboration with researchers from industry, academia, and national laboratories are investigating these and other novel and commercial ion exchangers for use in nuclear waste remediation of groundwater, HLW, and LLW. Since FY 1995, experimental work at PNNL has focused on small-scale batch distribution (K{sub d}) testing of numerous solid sorbents with actual and simulated Hanford wastes, chemical and radiolytic stability of various organic ion exchanger resins, bench-scale column ion exchange testing in actual and simulated Complexant Concentrate (CC) and Neutralized Current Acid Waste (NCAW), and Tc and Sr removal from groundwater and LLW. In addition, PNNL has continued to support various site demonstrations at the Idaho National Engineering Laboratory, Savannah River Site, West Valley Nuclear Services, Hanford N-Springs, and Hanford N-Basin using technologies developed by their industrial partners. This summary will focus on batch distribution results from the actual waste tests. The data collected in these development and testing tasks provide a rational basis for the selection and direct comparison of various ion exchange materials in simulated and actual HLW, LLW, and groundwater. In addition, prediction of large-scale column loading performance for the materials tested is possible using smaller volumes of actual waste solution. The method maximizes information while minimizing experimental expense, time, and laboratory and process wastes.

  10. Exchange-dependent relaxation in the rotating frame for slow and intermediate exchange -- modeling off-resonant spin-lock and chemical exchange saturation transfer.

    PubMed

    Zaiss, Moritz; Bachert, Peter

    2013-05-01

    Chemical exchange observed by NMR saturation transfer (CEST) and spin-lock (SL) experiments provide an MRI contrast by indirect detection of exchanging protons. The determination of the relative concentrations and exchange rates is commonly achieved by numerical integration of the Bloch-McConnell equations. We derive an analytical solution of the Bloch-McConnell equations that describes the magnetization of coupled spin populations under radiofrequency irradiation. As CEST and off-resonant SL are equivalent, their steady-state magnetization and dynamics can be predicted by the same single eigenvalue: the longitudinal relaxation rate in the rotating frame R1ρ . For the case of slowly exchanging systems, e.g. amide protons, the saturation of the small proton pool is affected by transverse relaxation (R2b ). It turns out, that R2b is also significant for intermediate exchange, such as amine- or hydroxyl-exchange or paramagnetic CEST agents, if pools are only partially saturated. We propose a solution for R1ρ that includes R2 of the exchanging pool by extending existing approaches, and verify it by numerical simulations. With the appropriate projection factors, we obtain an analytical solution for CEST and SL for nonzero R2 of the exchanging pool, exchange rates in the range 1-10(4) Hz, B1 from 0.1 to 20 μT and arbitrary chemical shift differences between the exchanging pools, whilst considering the dilution by direct water saturation across the entire Z-spectra. This allows the optimization of irradiation parameters and the quantification of pH-dependent exchange rates and metabolite concentrations. In addition, we propose evaluation methods that correct for concomitant direct saturation effects. It is shown that existing theoretical treatments for CEST are special cases of this approach.

  11. Adsorption of three pharmaceuticals on two magnetic ion-exchange resins.

    PubMed

    Jiang, Miao; Yang, Weiben; Zhang, Ziwei; Yang, Zhen; Wang, Yuping

    2015-05-01

    The presence of pharmaceuticals in aquatic environments poses potential risks to the ecology and human health. This study investigated the removal of three widely detected and abundant pharmaceuticals, namely, ibuprofen (IBU), diclofenac (DC), and sulfadiazine (SDZ), by two magnetic ion-exchange resins. The adsorption kinetics of the three adsorbates onto both resins was relatively fast and followed pseudo-second-order kinetics. Despite the different pore structures of the two resins, similar adsorption patterns of DC and SDZ were observed, implying the existence of an ion-exchange mechanism. IBU demonstrated a combination of interactions during the adsorption process. These interactions were dependent on the specific surface area and functional groups of the resin. The adsorption isotherm fittings verified the differences in the behavior of the three pharmaceuticals on the two magnetic ion-exchange resins. The presence of Cl- and SO4(2-) suppressed the adsorption amount, but with different inhibition levels for different adsorbates. This work facilitates the understanding of the adsorption behavior and mechanism of pharmaceuticals on magnetic ion-exchange resins. The results will expand the application of magnetic ion-exchange resins to the removal of pharmaceuticals in waters.

  12. Ion-exchange selectivity of diclofenac, ibuprofen, ketoprofen, and naproxen in ureolyzed human urine.

    PubMed

    Landry, Kelly A; Sun, Peizhe; Huang, Ching-Hua; Boyer, Treavor H

    2015-01-01

    This research advances the knowledge of ion-exchange of four non-steroidal anti-inflammatory drugs (NSAIDs) - diclofenac (DCF), ibuprofen (IBP), ketoprofen (KTP), and naproxen (NPX) - and one analgesic drug-paracetamol (PCM) - by strong-base anion exchange resin (AER) in synthetic ureolyzed urine. Freundlich, Langmuir, Dubinin-Astakhov, and Dubinin-Radushkevich isotherm models were fit to experimental equilibrium data using nonlinear least squares method. Favorable ion-exchange was observed for DCF, KTP, and NPX, whereas unfavorable ion-exchange was observed for IBP and PCM. The ion-exchange selectivity of the AER was enhanced by van der Waals interactions between the pharmaceutical and AER as well as the hydrophobicity of the pharmaceutical. For instance, the high selectivity of the AER for DCF was due to the combination of Coulombic interactions between quaternary ammonium functional group of resin and carboxylate functional group of DCF, van der Waals interactions between polystyrene resin matrix and benzene rings of DCF, and possibly hydrogen bonding between dimethylethanol amine functional group side chain and carboxylate and amine functional groups of DCF. Based on analysis of covariance, the presence of multiple pharmaceuticals did not have a significant effect on ion-exchange removal when the NSAIDs were combined in solution. The AER reached saturation of the pharmaceuticals in a continuous-flow column at varying bed volumes following a decreasing order of DCF > NPX ≈ KTP > IBP. Complete regeneration of the column was achieved using a 5% (m/m) NaCl, equal-volume water-methanol solution. Results from multiple treatment and regeneration cycles provide insight into the practical application of pharmaceutical ion-exchange in ureolyzed urine using AER.

  13. The nature of ion exchange selectivity of phenol-formaldehyde sorbents with respect to cesium and rubidium ions

    NASA Astrophysics Data System (ADS)

    Kargov, S. I.; Shelkovnikova, L. A.; Ivanov, V. A.

    2012-05-01

    The structure of aqua complexes of alkali metal ions Me+(H2O) n , n = 1-6, where Me is Li, Na, K, Rb, and Cs, and complexes of 2,6-dimethylphenolate anion (CH3)2PhO- selected as a model of the elementary unit of phenol-formaldehyde ion exchanger with hydrated alkali metal cations Me+(H2O) n , n = 0-5, was studied by the density functional method. The energies of successive hydration of the cations and the energies of binding of alkali metal hydrated cations with (CH3)2PhO- depending on the number of water molecules n were calculated. It was shown that the dimethylphenolate ion did not have specific selectivity with respect to cesium and rubidium ions. The energies of hydration and the energies of binding of alkali metal cations with (CH3)2PhO- decreased in the series Li+ > Na+ > K+ > Rb+ > Cs+ as n increased. The conclusion was drawn that the reason for selectivity of phenol-formaldehyde and other phenol compounds with respect to cesium and rubidium ions was the predomination of the ion dehydration stage in the transfer from an aqueous solution to the phenol phase compared with the stage of binding with ion exchange groups.

  14. Properties of nickel-cadmium separators. [ion exchange membrances

    NASA Technical Reports Server (NTRS)

    Lee, J.

    1977-01-01

    The thickness, moisture content, exchange capacity, tensile strength, diffusion characteristics, stability, and electrical properties are discussed for the 2291 radiation-grafted separator used in military vented nickel cadmium aircraft batteries. A regression analysis of separator resistance as a function of temperature and KOH concentration is included.

  15. Kilogram-scale purification of americium by ion exchange

    SciTech Connect

    Wheelwright, E.J.

    1980-05-01

    Sequential anion and cation exchange processes have been used for the final purification of /sup 241/Am recovered during the reprocessing of aged plutonium metallurgical scrap. Plutonium was removed by absorption on Dowex 1, X-3.5 (30 to 50 mesh) anion exchange resin from 6.5 to 7.5 M HNO/sub 3/ feed solution. Following a water dilution to 0.75 to 1.0 M HNO/sub 3/, americium was absorbed on Dowex 50W, X-8 (50 to 100 mesh) cation exchange resin. Final purification was accomplished by elution of the absorbed band down 3 to 4 successive beds of the same resin, preloaded with Zn/sup 2+/, with an NH/sub 4/OH buffered chelating agent. The recovery of mixed /sup 241/Am-/sup 243/Am from power reactor reprocessing waste has been demonstrated. Solvent extraction was used to recover a HNO/sub 3/ solution of mixed lanthanides and actinides from waste generated by the reprocessing of 13.5 tons of Shippingport Power Reactor blanket fuel. Sequential cation exchange band-displacement processes were then used to separate americium and curium from the lanthanides and then to separate approx. 60 g of /sup 244/Cm from 1000 g of mixed /sup 241/Am-/sup 243/Am.

  16. Tabulation and evaluation of ion exchange data on smectites, certain zeolites and basalt

    SciTech Connect

    Benson, L.V.

    1980-05-01

    An extensive search of the literature has been made for ion exchange data on smectites, certain zeolites and basalt. The data are in the form of thermodynamic equilibrium constants, corrected selectivity coefficients, and distribution coefficients. Room temperature alkali and alkaline earth metal cation ion exchange data for smectites are extensive. Correlation between the exchange free energies of alkali metal cations on Camp Berteau montmorillonite values with their Debeye-Hueckel parameter was found. Significant differences in values of exchange constants for the same reaction on different smectites were noted. While this in part may be attributable to differences in experimental procedures, much of the variance is probably due to differences in charge densities and the effective field strengths of the smectites. Differences in field strength are related to the type and amount of substitution on intercrystalline octahedral and tetrahedral sites. Data on smectites suggest that cation exchange selectivities are very strong functions of temperature. Experiments on the exchange properties of clinoptilolite and mordenite have been generally confined to alkali and alkaline earth cations although data for certain transition metal ions are also available for synthetic mordenite. The temperature dependences of zeolite exchange selectivities remain largely unknown. Distribution coefficients for groundwater-basalt systems have been measured for a variety of elements at temperatures up to 150/sup 0/C. Steady state concentrations are often never achieved either from the sorption or the desorption side. Classical models of ion exchange have been applied successfully to zeolite and smectite exchange reactions. The sorption behavior of a basalt is better treated with models of the interface which take surface ionization and complexation into account.

  17. Energy exchange via multi-species streaming in laser-driven ion acceleration

    NASA Astrophysics Data System (ADS)

    King, M.; Gray, R. J.; Powell, H. W.; Capdessus, R.; McKenna, P.

    2017-01-01

    Due to the complex electron dynamics and multiple ion acceleration mechanisms that can take place in the interaction of an ultra-intense laser pulse with a thin foil, it is possible for multiple charged particle populations to overlap in space with varying momentum distributions. In certain scenarios this can drive streaming instabilities such as the relativistic Buneman instability and the ion-ion acoustic instability. The potential for such instabilities to occur are demonstrated using particle-in-cell simulations. It is shown that if a population of ions can be accelerated such that it can propagate through other slowly expanding ion populations, energy exchange can occur via the ion-ion acoustic instability.

  18. Effect of the type of ion exchange membrane on performance, ion transport, and pH in biocatalyzed electrolysis of wastewater.

    PubMed

    Rozendal, R A; Sleutels, T H J A; Hamelers, H V M; Buisman, C J N

    2008-01-01

    Previous studies have shown that the application of cation exchange membranes (CEMs) in bioelectrochemical systems running on wastewater can cause operational problems. In this paper the effect of alternative types of ion exchange membrane is studied in biocatalyzed electrolysis cells. Four types of ion exchange membranes are used: (i) a CEM, (ii) an anion exchange membrane (AEM), (iii) a bipolar membrane (BPM), and (iv) a charge mosaic membrane (CMM). With respect to the electrochemical performance of the four biocatalyzed electrolysis configurations, the ion exchange membranes are rated in the order AEM > CEM > CMM > BPM. However, with respect to the transport numbers for protons and/or hydroxyl ions (t(H/OH)) and the ability to prevent pH increase in the cathode chamber, the ion exchange membranes are rated in the order BPM > AEM > CMM > CEM.

  19. Magnetic Exchange Interaction between Rare-Earth and Mn Ions in Multiferroic Hexagonal Manganites

    NASA Astrophysics Data System (ADS)

    Talbayev, D.; Laforge, A. D.; Trugman, S. A.; Hur, N.; Taylor, A. J.; Averitt, R. D.; Basov, D. N.

    2008-12-01

    We report a study of magnetic dynamics in multiferroic hexagonal manganite HoMnO3 by far-infrared spectroscopy. The low-temperature magnetic excitation spectrum of HoMnO3 consists of magnetic-dipole transitions of Ho ions within the crystal-field split J=8 manifold and of the triangular antiferromagnetic resonance of Mn ions. We determine the effective spin Hamiltonian for the Ho ion ground state. The magnetic-field splitting of the Mn antiferromagnetic resonance allows us to measure the magnetic exchange coupling between the rare-earth and Mn ions.

  20. Magnetic exchange interaction between rare-earth and Mn ions in multiferroic hexagonal manganites

    SciTech Connect

    Talbayev, Diyar; Trugman, Stuart A; Taylor, Antoinette J; Averitt, Richard D; Namjung, Hur; Andrew, Laforge D; Dimitri, Basov N

    2008-01-01

    The authors report a study of magnetic dynamics in multiferroic hexagonal manganite HoMnO{sub 3} by far-infrared spectroscopy. Low-temperature magnetic excitation spectrum of HoMnO{sub 3} consists of magnetic-dipole transitions of Ho ions within the crystal-field split J = 8 manifold and of the triangular antiferromagnetic resonance of Mn ions. They determine the effective spin Hamiltonian for the Ho ion ground state. The magnetic-field splitting of the Mn antiferromagnetic resonance allows us to measure the magnetic exchange coupling between the rare-earth and Mn ions.

  1. Modification of the saturation magnetization of exchange bias thin film systems upon light-ion bombardment

    NASA Astrophysics Data System (ADS)

    Huckfeldt, Henning; Gaul, Alexander; Müglich, Nicolas David; Holzinger, Dennis; Nissen, Dennis; Albrecht, Manfred; Emmrich, Daniel; Beyer, André; Gölzhäuser, Armin; Ehresmann, Arno

    2017-03-01

    The magnetic modification of exchange bias materials by ‘ion bombardment induced magnetic patterning’ has been established more than a decade ago. To understand these experimental findings several theoretical models were introduced. Few investigations, however, did focus on magnetic property modifications caused by effects of ion bombardment in the ferromagnetic layer. In the present study, the structural changes occurring under ion bombardment were investigated by Monte-Carlo simulations and in experiments. A strong reduction of the saturation magnetization scaling linearly with increasing ion doses is observed and our findings suggest that it is correlated to the swelling of the layer material based on helium implantation and vacancy creation.

  2. Film model approximation for particle-diffusion-controlled binary ion exchange

    SciTech Connect

    Carta, G.; Cincotti, A.; Cao, G.

    1999-01-01

    A new rate expression for particle-diffusion-controlled ion exchange, based on an equivalent pseudosteady-state film resistance model, is developed. The rate expression approximates the electric field effects on intraparticle diffusion in spherical ion-exchangers. With regard to the prediction of batch exchange and column breakthrough curves for both irreversible and reversible processes, the model captures the essential traits of the coupled diffusion phenomenon described by the Nernst-Planck equation with results of accuracy comparable to that obtained when using the linear driving force approximation for systems with constant diffusivity. Numerical results for the exchange of two counterions of equal valence are presented as application examples for different mobility ratios and selectivity coefficients.

  3. METHOD OF SEPARATING RARE EARTHS BY ION EXCHANGE

    DOEpatents

    Spedding, F.H.; Powell, J.E.

    1960-10-18

    A process is given for separating yttrium and rare earth values having atomic numbers of from 57 through 60 and 68 through 71 from an aqueous solution whose pH value can range from 1 to 9. All rare earths and yttrium are first adsorbed on a cation exchange resin, and they are then eluted with a solution of N-hydroxyethylethylenediaminetriacetic acid (HEDTA) in the order of decreasing atomic number, yttrium behaving like element 61; the effluents are collected in fractions. The HEDTA is recovered by elution with ammonia solution and the resin is regenerated with sulfuric acid. Rare earths are precipitated from the various effluents with oxalic acid, and each supernatant is passed over cation exchange resin for adsorption of HEDTA and nonprecipitated rare earths: the oxalic acid is not retained by the resin.

  4. Quantitative description of ion transport in Donnan ion exchange membrane systems

    SciTech Connect

    Rush, W.E.; Baker, B.L.

    1980-05-01

    Presented are simplified mass transfer techniques describing the transfer of ions in continuous ion selective membrane systems in which the resistance to ion transport through the membrane is small in relation to the resistance to ion transport in the solution phase. Methods are developed through the application of the transfer unit concept to the Donnan equilibrium. This equilibrium describes the equilibrium ion concentration on either side of an ion selective membrane. Data from one cation selection system is presented as evidence of the validity of these methods. Further techniques are shown that will allow the determination of ion transport given only equipment parameters and solution diffusivities. Supporting data are shown.

  5. SEPARATION OF PLUTONIUM FROM AQUEOUS SOLUTIONS BY ION-EXCHANGE

    DOEpatents

    Schubert, J.

    1958-06-01

    A process is described for the separation of plutonium from an aqueous solution of a plutonium salt, which comprises adding to the solution an acid of the group consisting of sulfuric acid, phosphoric acid, and oxalic acid, and mixtures thereof to provide an acid concentration between 0.0001 and 1 M, contacting the resultant solution with a synthetic organic anion exchange resin, and separating the aqueous phase and the resin which contains the plutonium.

  6. Building 579 waste ion exchange facility characterization report

    SciTech Connect

    Sholeen, C.M.; Geraghty, D.C.

    1997-03-01

    External direct surveys were performed for elevated {gamma} levels with a PG2 portable detector connected to a PRM 5-3 meter and for elevated {alpha} and {beta} levels with an NE portable detector. No {gamma} activity above background was detected. Several locations, the floor and west wall of building 579 and the manhole, had low levels of {beta} activity, up to 87 {+-} 49 dis/min. These values are below the allowable residual surface contamination limits for removable beta activity. There is water in the Mixed Bed Exchange Vessel, the Cation Exchange Vessel, the Closed Drain Tank, the manhole and some of the pipes. The accessible internal surfaces of the pipes, tanks and columns had higher levels of {beta} activity up to 172 {+-} 52 dis/min and some {alpha} activity up to 106 {+-} 29 dis/min. After the water is removed from the vessels, tanks, and lines, they should be surveyed to determine whether the areas accessible for smear surveys are representative of the general inside contamination levels. There are elevated levels of radionuclides in the resin from the Cation Exchange Vessel and in the water from the manhole. Since the radionuclide concentrations in the manhole water are less than ten times the site release criteria, it does not need any processing before it is released to the onsite drains. Although there are RCRA metals on the resin in the Cation Exchange Vessel, the amount that is removed during a leaching analysis is below the toxicity Characteristic level. Therefore, the resin is a radioactive waste not a mixed waste.

  7. Structure-Functional Basis of Ion Transport in Sodium–Calcium Exchanger (NCX) Proteins

    PubMed Central

    Giladi, Moshe; Shor, Reut; Lisnyansky, Michal; Khananshvili, Daniel

    2016-01-01

    The membrane-bound sodium–calcium exchanger (NCX) proteins shape Ca2+ homeostasis in many cell types, thus participating in a wide range of physiological and pathological processes. Determination of the crystal structure of an archaeal NCX (NCX_Mj) paved the way for a thorough and systematic investigation of ion transport mechanisms in NCX proteins. Here, we review the data gathered from the X-ray crystallography, molecular dynamics simulations, hydrogen–deuterium exchange mass-spectrometry (HDX-MS), and ion-flux analyses of mutants. Strikingly, the apo NCX_Mj protein exhibits characteristic patterns in the local backbone dynamics at particular helix segments, thereby possessing characteristic HDX profiles, suggesting structure-dynamic preorganization (geometric arrangements of catalytic residues before the transition state) of conserved α1 and α2 repeats at ion-coordinating residues involved in transport activities. Moreover, dynamic preorganization of local structural entities in the apo protein predefines the status of ion-occlusion and transition states, even though Na+ or Ca2+ binding modifies the preceding backbone dynamics nearby functionally important residues. Future challenges include resolving the structural-dynamic determinants governing the ion selectivity, functional asymmetry and ion-induced alternating access. Taking into account the structural similarities of NCX_Mj with the other proteins belonging to the Ca2+/cation exchanger superfamily, the recent findings can significantly improve our understanding of ion transport mechanisms in NCX and similar proteins. PMID:27879668

  8. Organic Modification of a Layered Silicate by Co-Ion Exchange of an Alkyl Ammonium and a Mono-Protonated Diamine

    NASA Technical Reports Server (NTRS)

    Campbell, Sandi G. (Inventor)

    2004-01-01

    Co-Ion exchange of the interlayer cations of a layered silicate with a mono-protonated aromatic diamine and an alkyl ammonium ion into the silicate galleries. The presence of the alkyl ammonium ion provides low oligomer melt viscosity during processing. The presence of the diamine allows chemical reaction between the silicate surface modification and the monomers. This reaction strengthens the polymer silicate interface, and ensures irreversible separation of the individual silicate layers. Improved polymer thermal oxidative stability and mechanical properties are obtained.

  9. RESORCINOL-FORMALDEHYDE ION EXCHANGE RESIN CHEMISTRY FOR HIGH LEVEL WASTE TREATMENT

    SciTech Connect

    Nash, C.; Duignan, M.

    2010-01-14

    A principal goal at the Savannah River Site is to safely dispose of the large volume of liquid nuclear waste held in many storage tanks. In-tank ion exchange technology is being considered for cesium removal using a polymer resin made of resorcinol formaldehyde that has been engineered into microspheres. The waste under study is generally lower in potassium and organic components than Hanford waste; therefore, the resin performance was evaluated with actual dissolved salt waste. The ion exchange performance and resin chemistry results are discussed.

  10. Ion-exchange characteristics of sodium-calcium-silicate glass: Calculation from mode spectra

    NASA Astrophysics Data System (ADS)

    Zhurikhina, V. V.; Petrov, M. I.; Sokolov, K. S.; Shustova, O. V.

    2010-10-01

    The characteristics of silver-sodium ion exchange in standard commercial sodium-calcium-silicate glass are investigated using mode spectroscopy. The activation energy of the process, the silver-sodium interdiffusion coefficient, and the dependence of the maximal modulation of the refractive index on the silver nitrate concentration in the experimental salt bath are determined. The data set presented here makes it possible to specify the conditions for the formation of ion-exchange optical structures with preset parameters based on the glasses studied here.

  11. Ion exchange membrane textile bioreactor as a new alternative for drinking water denitrification.

    PubMed

    Berdous, Dalila; Akretche, Djamal-Eddine; Abderahmani, Ahmed; Berdous, Sakina; Meknaci, Rima

    2014-06-01

    This work enters in the optics of the denitrification of a polluted water by two membrane techniques, the Donnan dialysis (DD) and the ion exchange membrane bioreactor (IEMB), using a conventional barrier, composed by an anion exchange membrane (AEM), and a hybrid barrier, where the AEM is combined to an anion exchange textile (AET). The effects of the hydrodynamic factor and the nature of the carbon source on the transfer and the reduction of nitrate ions were studied. The study results obtained through the DD showed the effectiveness of the hybrid barrier in the recovery and concentration of nitrate ions. This was also recorded during denitrification by the hybrid process, called the ion exchange membrane textile bioreactor (IEMTB), with a significant reduction of nitrates, compared to IEMB, due to the efficiency of the Pseudomonas aeruginosa biofilm formed at the surface of the AET. Here, the permselectivity of the membrane and the good bioreduction of the pollutants are no longer major conditions to the better performance of the process. The application of IEMTB in the denitrification of groundwater, having a nitrate concentration of 96.67 ppm, shows a total reduction of nitrate ions without changing the quality of the water. Indeed, the analysis of the recovered water, or yet the treated water, shows the absence of the bacterium by-products and concentrations in the nitrates and nitrites which are, respectively, equal to 0.02±0.01 ppm, and inferiors to the detection limit (<0.02 ppm).

  12. Copper effects on ion transport across lamprey erythrocyte membrane: Cl(-)/OH(-) exchange induced by cuprous ions.

    PubMed

    Bogdanova, A Y; Virkki, L V; Gusev, G P; Nikinmaa, M

    1999-09-15

    We studied the effects of prelytic copper concentrations on cell volume, intracellular pH, and ion transport in lamprey erythrocytes. Ion fluxes and pH were measured by radioactive tracer technique, patch clamp, and flame photometry. Prelytic CuSO(4) concentration of 100 microM caused anion-dependent intracellular acidification and increase in Cl(-) influx after 2 min lag-phase. In the presence of ascorbate copper effect was amplified and lag-phase was skipped. Pretreatment of the cells with N-phenyl maleimide abolished copper-induced changes completely. Copper treatment caused an increase in Na(+) fluxes in both directions and a net Na(+) uptake. Copper-induced Na(+) transport was partially amiloride(MIA)-sensitive representing Na(+)/H(+) exchange. The nature of the amiloride-insensitive fraction of copper-activated Na(+) influx remains unknown. Cell swelling after 15 min of copper exposure induced regulatory volume decrease response involving KCl extrusion via K(+) and Cl(-) volume-sensitive channels. We suggest that the effects of copper on ion transport fit the following sequence of events: (i) cupric ions are reduced to cuprous state on the membrane surface, (ii) electroneutral pairs CuCl and CuOH mediate chloride/hydroxyl exchange, as shown before for trialkyltin, dissipating transmembrane pH gradient, and (iii) changes in intracellular pH result in the activation of the Na(+)/H(+) exchange and consecutive volume changes cause the RVD response.

  13. Improved durability of proton exchange membrane fuel cells by introducing Sn (IV) oxide into electrodes using an ion exchange method

    NASA Astrophysics Data System (ADS)

    Poulsen, M. G.; Larsen, M. J.; Andersen, S. M.

    2017-03-01

    Electrodes of Proton Exchange Membrane Fuel Cells (PEMFCs), consisting of catalyst-coated gas diffusion layers, were subjected to an optimized ion exchange procedure, in which tin (IV) oxide (SnO2) nanoparticles were introduced into them. Both methanol and sulfuric acid were tested as ion exchange solvents. SnO2 has previously been shown to exhibit radical scavenging abilities towards radicals inside the electrocatalyst layers. Its presence inside the electrodes was confirmed using X-ray photoelectron spectroscopy and X-ray fluorescence. After exposure to an accelerated stress test in a three-electrode setup, the electrodes containing SnO2 were found to have retained approximately 73.0% of their original Pt, while only 53.2% was retained in electrodes treated identically, but without Sn. Similarly, the SnO2-treated electrodes also experienced a smaller loss in electrochemical surface area in comparison to before the accelerated stress test. A membrane electrode assembly (MEA) constructed with a SnO2-containing anode was evaluated over 500 h. The results showed remarkably reduced OCV decay rate and end of test hydrogen crossover compared to the control MEA, indicating that SnO2 aids in impeding membrane thinning and pinhole formation. The results point toward a positive effect of SnO2 on fuel cell durability, by reducing the degradation of the membrane as well as of the ionomer in the electrocatalyst layer.

  14. Predicting Carbonate Ion Transport in Alkaline Anion Exchange Materials

    DTIC Science & Technology

    2012-01-01

    Schematic of the permeation cell experiment used to measure transient CO2 flux across the polymer electrolyte membrane. Experimental result vs. model trend...Microstructure on Charge Transfer, Mass Transfer, and Electrochemical Reactions in Solid Oxide Fuel Cells ; Part 2. Ion and Water Transport in Alkaline Anion...through the use of the Fuel Cell Technologies Test Station such as the relative humidity and flow rate of the feed gases, the cell temperature, and the

  15. Denitration of Rocky Flats Ion-Exchange Resins: Recommendation of Denitration Processes, October 19, 1995

    SciTech Connect

    Jacob Espinoza; Mary Barr; Wayne Smith

    1998-12-01

    Resin denitration via anion-exchange is an implementable process that can effectively mitigate the hazards associated with stored resins in which the bulk of the nitrate consists of an "exchangeable nitrate" ionically bound to the cationic sites of the anion-exchange resins. Salicylate has been selected as the exchange anion of choice because of its superior selectivity for the Rocky Flats resins and its unique potential for comprehensive recovery and recycle. This report outlines a single recommended resin denigration procedure that is reasonably independent of the resin composition and the current stored form. This procedure is not optimized but rather seeks to `over-treat' the resins so that a single procedure works for the variety of stored resins. The recommended treatment with sodium salicylate reduces resins by 95-99+% the measured exothermic behavior of the ion-exchange.

  16. Ultrafast fluxional exchange dynamics in electrolyte solvation sheath of lithium ion battery

    NASA Astrophysics Data System (ADS)

    Lee, Kyung-Koo; Park, Kwanghee; Lee, Hochan; Noh, Yohan; Kossowska, Dorota; Kwak, Kyungwon; Cho, Minhaeng

    2017-03-01

    Lithium cation is the charge carrier in lithium-ion battery. Electrolyte solution in lithium-ion battery is usually based on mixed solvents consisting of polar carbonates with different aliphatic chains. Despite various experimental evidences indicating that lithium ion forms a rigid and stable solvation sheath through electrostatic interactions with polar carbonates, both the lithium solvation structure and more importantly fluctuation dynamics and functional role of carbonate solvent molecules have not been fully elucidated yet with femtosecond vibrational spectroscopic methods. Here we investigate the ultrafast carbonate solvent exchange dynamics around lithium ions in electrolyte solutions with coherent two-dimensional infrared spectroscopy and find that the time constants of the formation and dissociation of lithium-ion...carbonate complex in solvation sheaths are on a picosecond timescale. We anticipate that such ultrafast microscopic fluxional processes in lithium-solvent complexes could provide an important clue to understanding macroscopic mobility of lithium cation in lithium-ion battery on a molecular level.

  17. Effect of diffusion potential, osmosis and ion-exchange on transdermal drug delivery: theory and experiments.

    PubMed

    Hirvonen, J; Murtomäki, L; Kontturi, K

    1998-12-04

    Equations expressing the effect of the diffusion potential on the trace ion transfer across a porous charged membrane have been derived. These equations have been tested with experiments with human cadaver skin. The transfer of sotalol and salicylate was measured varying the salt (NaCl) concentration in the donor and receiver compartments. It appears that osmotic pressure and ion-exchange make a significant contribution to the flux enhancement by the diffusion potential.

  18. Deuterium retention in tungsten after heavy ion damage and hydrogen isotope exchange in PISCES

    NASA Astrophysics Data System (ADS)

    Barton, J. L.; Wang, Y. Q.; Dittmar, T.; Doerner, R. P.; Tynan, G. R.

    2014-08-01

    The effect of H isotope exchange and radiation damage on the retention of D in W was examined in the PISCES linear plasma device. W samples were treated with D plasma at low sample temperatures (473 K), with a fluence of 1026 ions/m2 and ion energies of 150 eV. Each sample was then exposed to varying doses of H plasma with similar sample temperature and plasma conditions to fluences ranging from 0 to 1026 ions/m2, to examine the effectiveness of isotope exchange as a means of tritium removal. The D(3He, p)4He nuclear reaction was used to measure D concentration profiles up to a depth of 7.7 μm. Thermal desorption spectroscopy (TDS) was used to determine the D retained throughout the bulk of the sample. Isotope exchange allows for a unique study of atomic migration by separately examining the diffusion of implanted atoms from those bombarding the surface. D atoms are exchanged out of traps as a result of H plasma bombardment and diffuse until either falling into another trap or reaching the surface to recombine and escape. Radiation damage at levels of 0.01, 0.1, and 1 displacements per atom (dpa) was carried out before plasma exposure on some samples with 2 MeV Cu ions as a surrogate for damage caused by fusion neutrons. The Cu ion damage was compared to damage induced by 6 MeV W ions to see if there is an effect of Cu contamination on retention. We saw little difference in Cu versus W ion damage at low dpa, but at 1 dpa, where Cu content reached 65 appm, contamination seems to be significant. Retention measurements showed that ion damage has little effectiveness on isotope removal at these sample temperatures; however, there is evidence to suggest that the trapping mechanisms in W change as damage is increased.

  19. Effect of formaldehyde on Cu(II) removal from synthetic complexed solutions by ion exchange.

    PubMed

    Juang, Ruey-Shin; Lin, Su-Hsia; Kao, Hsiang-Chien; Theng, Ming-Huei

    2005-06-01

    The effect of formaldehyde (HCHO) on the ion exchange of Cu(II) from an equimolar EDTA (ethylenediaminetetraacetic acid, H(4)L) solution with a strong-base Amberlite IRA-400 resin was studied. Experiments were conducted as a function of the initial concentration of Cu(II) (0.5-10 mM), solution pH (1.0-6.0), HCHO concentration (0-6 vol%), and temperature (15-35 degrees C). It was shown that the amount of exchange of Cu(II), which exists in the form of complexed anions CuL(2-), increased with increasing solution pH and reached a plateau at an equilibrium pH (pH(e)) of 3.5. However, the amount of exchange decreased with increasing HCHO concentration up to 3 vol% but then slightly decreased with a further increase in HCHO concentration. Such effect of added HCHO was determined by the following two factors: the competitive exchange of HCOO(-) anions and the enhanced exchange of Cu(I) in the form of complexed anions CuL(3-). The exchange isotherm obtained at a fixed pH(e) could be well described by the Langmuir equation. The isosteric enthalpy change for the present ion exchange process was also evaluated and discussed.

  20. DEVELOPMENT OF AN APPROACH TO MODELING LOADING AND ELUTION OF SPHERICAL RESORCINOL FORMALDEHYDE ION-EXCHANGE RESIN

    SciTech Connect

    Aleman, S.; Hamm, L.; Smith, F.

    2011-10-03

    The current strategy for removal of cesium from the Hanford waste stream is ion-exchange using spherical Resorcinol-Formaldehyde (sRF) resin. The original resin of choice was granular SuperLig 644 resin and during testing of this resin several operational issues were identified. For example, the granular material had a high angle of internal friction resulting in fragmentation of resin particles along its edges during cycling and adverse hydraulic performance. Efforts to replace SuperLig 644 were undertaken and one candidate was the granular Resorcinol-Formaldehyde (RF) resin where experience with this cation exchanger dates back to the late 1940's. To minimize hydraulic concerns a spherical version of RF was developed and several different chemically produced batches were created. The 5E-370/641 batch of sRF was selected and for the last decade numerous studies have been performed (e.g., batch contact tests, column loading and elution tests). The Waste Treatment Plant (WTP) flowsheet shows that the aqueous phase waste stream will have a wide range of ionic concentrations (e.g., during the loading step 0-3 M free OH, 5+ M Na, 0-1 M K, 0-3 M NO{sub 3}). Several steps are required in the ion-exchange process to achieve the required Cs separation factors: loading, displacement, washing, elution, and regeneration. The sRF resin will be operated over a wide range in pH (i.e., pH of 12-14 during the loading step and pH of 0.01-1 during the elution step). During some of these steps very high levels of counter-ions and co-ions will be present within the aqueous phase. Alternative process feeds are under consideration as well (e.g., sodium levels as high as 8 M and column operation up to 45 C during loading, reduced and recycled HNO{sub 3} during elution). In order to model the performance of sRF resin through an entire ion-exchange cycle, a more robust isotherm model is required. To achieve this more robust isotherm model requires knowledge of the numbers and kinds of

  1. The bacterial chemical repertoire mediates metabolic exchange within gut microbiomes.

    PubMed

    Rath, Christopher M; Dorrestein, Pieter C

    2012-04-01

    Microbial communities in the gut have been hypothesized to play key roles in the health of the host organism. Exploring the relationship between these populations and disease states has been a focus of the human microbiome project. However, the biological roles of the compounds produced by the gut bacteria are largely unknown. We hypothesize that these compounds act as metabolic exchange factors-mediating inter-species and intra-species interactions in the microbiome. This view is supported through this review of known bacterial metabolic exchange factors and evidence for uncharacterized metabolic exchange factors in the gut. The impact of model systems and technological developments in exploring this hypothesis are also discussed. Together, these investigations are revolutionizing our understanding of the gut microbiome-presenting the possibility of identifying new strategies for treating disease in the host.

  2. Experiments with an ion-neutral hybrid trap: cold charge-exchange collisions

    NASA Astrophysics Data System (ADS)

    Smith, W. W.; Goodman, D. S.; Sivarajah, I.; Wells, J. E.; Banerjee, S.; Côté, R.; Michels, H. H.; Mongtomery, J. A.; Narducci, F. A.

    2014-01-01

    Due to their large trap depths (˜1 eV or 10,000 K), versatility, and ease of construction, Paul traps have important uses in high-resolution spectroscopy, plasma physics, and precision measurements of fundamental constants. An ion-neutral hybrid trap consisting of two separate but spatially concentric traps [a magneto-optic trap (MOT) for the neutral species and a mass-selective linear Paul trap for the ionic species] is an ideal apparatus for sympathetic cooling. However, over the past few years, hybrid traps have proven most useful in measuring elastic and charge-exchange rate constants of ion-neutral collisions over a wide temperature range from kilo-Kelvin to nano-Kelvin. We report some initially surprising results from a hybrid trap system in our laboratory where we have loaded the Paul trap with Ca+ ions in the presence of a Na MOT (localized dense gas of cold Na atoms). We find a strong loss of Ca+ ions with MOT exposure, attributed to an exothermic, non-resonant ion-neutral charge-exchange process with an activation barrier, which leads to the formation of Na+ ions. We propose a detailed mechanism for this process. We obtain an estimated measure of the rate constant for this charge exchange of ˜2 × 10-11 cm3/s, much less than the Langevin rate, which suggests that the Langevin assumption of unit efficiency in the reaction region is not correct in this case.

  3. Modeling ion exchange in glass with concentration-dependent diffusion coefficients and mobilities

    NASA Astrophysics Data System (ADS)

    Lupascu, Alexandru I.; Kevorkian, Antoine P.; Boudet, Thierry; Saint-Andre, Francoise; Persegol, Dominique; Levy, Michel

    1996-06-01

    Multimode buried waveguides made in silicate glass by field-assisted ion exchange present very asymmetric profiles. We show how this phenomenon originates in the large dependence of the kinetics on the local ion concentrations. For this purpose, we derive an interdiffusion equation that includes the effects of concentration-dependent diffusion coefficients and mobilities. We show how to deduce this dependence from measurements on ion- diffused samples. The maximum concentration of the incoming ions is computed from surface equilibrium conditions and is used in the interdiffusion equation as a limiting parameter for coefficient variations. To control the model accuracy for surface as well as buried waveguides, we measure ion profiles with three independent methods: M-lines, scanning electron microscopy, and near-field refractometry. When applied to Ag+-Na+ exchange in silicate glass, the model yields theoretical estimations in good agreement with experiments. This approach underlines the fundamentally nonlinear process that takes place during ion exchange and is also valuable to properly model singlemode waveguide fabrication.

  4. Effects of the spaces available for cations in strongly acidic cation-exchange resins on the exchange equilibria by quaternary ammonium ions and on the hydration states of metal ions.

    PubMed

    Watanabe, Yuuya; Ohnaka, Kenji; Fujita, Saki; Kishi, Midori; Yuchi, Akio

    2011-10-01

    The spaces (voids) available for cations in the five exchange resins with varying exchange capacities and cross-linking degrees were estimated, on the basis of the additivity of molar volumes of the constituents. Tetraalkylammonium ions (NR(4)(+); R: Me, Et, Pr) may completely exchange potassium ion on the resin having a larger void radius. In contrast, the ratio of saturated adsorption capacity to exchange capacity of the resin having a smaller void radius decreased with an increase in size of NR(4)(+) ions, due to the interionic contacts. Alkali metal ions could be exchanged quantitatively. While the hydration numbers of K(+), Rb(+), and Cs(+) were independent of the void radius, those of Li(+) and Na(+), especially Na(+), decreased with a decrease in void radius. Interionic contacts between the hydrated ions enhance the dehydration. Multivalent metal ions have the hydration numbers, comparable to or rather greater than those in water. A greater void volume available due to exchange stoichiometry released the interionic contacts and occasionally promoted the involvement of water molecules other than directly bound molecules. The close proximity between ions in the conventional ion-exchange resins having higher exchange capacities may induce varying interactions.

  5. Predicting Salt Permeability Coefficients in Highly Swollen, Highly Charged Ion Exchange Membranes.

    PubMed

    Kamcev, Jovan; Paul, Donald R; Manning, Gerald S; Freeman, Benny D

    2017-02-01

    This study presents a framework for predicting salt permeability coefficients in ion exchange membranes in contact with an aqueous salt solution. The model, based on the solution-diffusion mechanism, was tested using experimental salt permeability data for a series of commercial ion exchange membranes. Equilibrium salt partition coefficients were calculated using a thermodynamic framework (i.e., Donnan theory), incorporating Manning's counterion condensation theory to calculate ion activity coefficients in the membrane phase and the Pitzer model to calculate ion activity coefficients in the solution phase. The model predicted NaCl partition coefficients in a cation exchange membrane and two anion exchange membranes, as well as MgCl2 partition coefficients in a cation exchange membrane, remarkably well at higher external salt concentrations (>0.1 M) and reasonably well at lower external salt concentrations (<0.1 M) with no adjustable parameters. Membrane ion diffusion coefficients were calculated using a combination of the Mackie and Meares model, which assumes ion diffusion in water-swollen polymers is affected by a tortuosity factor, and a model developed by Manning to account for electrostatic effects. Agreement between experimental and predicted salt diffusion coefficients was good with no adjustable parameters. Calculated salt partition and diffusion coefficients were combined within the framework of the solution-diffusion model to predict salt permeability coefficients. Agreement between model and experimental data was remarkably good. Additionally, a simplified version of the model was used to elucidate connections between membrane structure (e.g., fixed charge group concentration) and salt transport properties.

  6. Mechanical compaction of smectite clays increases ion exchange selectivity for cesium.

    PubMed

    van Loon, Luc R; Glaus, Martin A

    2008-03-01

    A key discussion in radioactive waste disposal is the question of whether adsorption behavior of radionuclides in dispersed and in highly compacted materials is similar. It is common practice to measure sorption data on dispersed systems and to use these data to predict the sorption in compacted systems. The latter represent the situation in a real, deep geological repository system. The discussions focus mainly on items such as the effect of compaction on the accessibility of sorption sites, that is, on sterical effects, and not on the effect of compaction on the thermodynamics of the sorption processes. Here we show that in the case of sorption of cesium on sodium bentonite, material compaction indeed affects the thermodynamics of the sorption process such that sorption increases. This increase is due to a reduction of the interlayer space, leading to a lower ability of the interlayer water for cation hydration. Cations with a low hydration tendency, such as cesium, therefore accumulate in the interlayer space, whereas highly hydrated cations such as sodium tends to accumulate in the bulk water where water is easily available for hydration. The fact that mechanical compaction affects the thermodynamics of ion exchange processes in clay is an important finding and brings in a new aspect in the discussion on the transferability of thermodynamic data from diluted to compacted systems. The common practice of applying chemical and thermodynamic concepts valid for diluted systems to compacted systems must be basically scrutinized.

  7. Chemically Induced Phase Transformation in Austenite by Focused Ion Beam

    NASA Astrophysics Data System (ADS)

    Basa, Adina; Thaulow, Christian; Barnoush, Afrooz

    2013-11-01

    A highly stable austenite phase in a super duplex stainless steel was subjected to a combination of different gallium ion doses at different acceleration voltages. It was shown that contrary to what is expected, an austenite to ferrite phase transformation occurred within the focused ion beam (FIB) milled regions. Chemical analysis of the FIB milled region proved that the gallium implantation preceded the FIB milling. High resolution electron backscatter diffraction analysis also showed that the phase transformation was not followed by the typical shear and plastic deformation expected from the martensitic transformation. On the basis of these observations, it was concluded that the change in the chemical composition of the austenite and the local increase in gallium, which is a ferrite stabilizer, results in the local selective transformation of austenite to ferrite.

  8. Localised doping of Li-silicate glasses by Er 3+ ion exchange to fabricate thin optical layers

    NASA Astrophysics Data System (ADS)

    Salavcova, Linda; Spirkova, Jarmila; Mika, Martin; Mackova, Anna; Oswald, Jiri; Langrova, Anna; Vacik, Jiri

    2007-03-01

    Here we present a new method of fabrication of erbium containing thin optical layers that could be interesting for photonics active structures. These layers were fabricated by a purely thermal ion-exchange process at temperatures above the transformation point of the used glasses to minimise internal strain that arose in the layers during the fabrication process. In order to accelerate migration of rather immobile Er3+ ions, we used substrates with a high content of easily exchangeable Li+ ions. The substrates were prepared either as specially designed Li-glasses or glasses with intentionally created Li-containing surface layers. A number of nuclear analytical methods (i.e., Rutherford backscattering spectroscopy-RBS, and neutron depth profiling-NDP), as well as scanning electron microscopy (SEM-EDAX) were used to confirm presence of erbium in the glass surface and to determine the chemical composition of the fabricated layers. Photoluminescence spectra of the fabricated samples were measured to examine desired emission at the wavelength of 1.5 μm.

  9. Comprehensive analysis of pharmaceutical products using simultaneous mixed-mode (ion-exchange/reversed-phase) and hydrophilic interaction liquid chromatography.

    PubMed

    Kazarian, Artaches A; Nesterenko, Pavel N; Soisungnoen, Phimpha; Burakham, Rodjana; Srijaranai, Supalax; Paull, Brett

    2014-08-01

    Liquid chromatographic assays were developed using a mixed-mode column coupled in sequence with a hydrophilic interaction liquid chromatography column to allow the simultaneous comprehensive analysis of inorganic/organic anions and cations, active pharmaceutical ingredients, and excipients (carbohydrates). The approach utilized dual sample injection and valve-mediated column switching and was based upon a single high-performance liquid chromatography gradient pump. The separation consisted of three distinct sequential separation mechanisms, namely, (i) ion-exchange, (ii) mixed-mode interactions under an applied dual gradient (reversed-phase/ion-exchange), and (iii) hydrophilic interaction chromatography. Upon first injection, the Scherzo SS C18 column (Imtakt) provided resolution of inorganic anions and cations under isocratic conditions, followed by a dual organic/salt gradient to elute active pharmaceutical ingredients and their respective organic counterions and potential degradants. At the top of the mixed-mode gradient (high acetonitrile content), the mobile phase flow was switched to a preconditioned hydrophilic interaction liquid chromatography column, and the standard/sample was reinjected for the separation of hydrophilic carbohydrates, some of which are commonly known excipients in drug formulations. The approach afforded reproducible separation and resolution of up to 23 chemically diverse solutes in a single run. The method was applied to investigate the composition of commercial cough syrups (Robitussin®), allowing resolution and determination of inorganic ions, active pharmaceutical ingredients, excipients, and numerous well-resolved unknown peaks.

  10. Time-dependence ion charge state distributions of vacuum arcs: An interpretation involving atoms and charge exchange collisions

    SciTech Connect

    Anders, Andre

    2004-08-27

    Experimentally observed charge state distributions are known to be higher at the beginning of each arc discharge. Up to know, this has been attributed to cathode surface effects in terms of changes of temperature, chemical composition and spot mode. Here it is shown that the initial decay of charge states of cathodic arc plasmas may at least in part due to charge exchange collisions of ions with neutrals that gradually fill the discharge volume. Sources of neutrals may include evaporated atoms from macroparticles and still-hot craters of previously active arc spots. More importantly, atoms are also produced by energetic condensation of the cathodic arc plasma. Self-sputtering is significant when ions impact with near-normal angle of incidence, and ions have low sticking probability when impacting at oblique angle of incidence. Estimates show that the characteristic time for filling the near-cathode discharge volume agrees well with the charge state decay time, and the likelihood of charge exchange is reasonably large to be taken into account.

  11. Chemical ions affect survival of avian cholera organisms in pondwater

    USGS Publications Warehouse

    Price, J.I.; Yandell, B.S.; Porter, W.P.

    1992-01-01

    Avian cholera (Pasteurella multocida) is a major disease of wild waterfowl, but its epizootiology remains little understood. Consequently, we examined whether chemical ions affected survival of avian cholera organisms in water collected from the Nebraska Rainwater Basin where avian cholera is enzootic. We tested the response of P. multocida to ammonium (NH4), calcium (Ca), magnesium (Mg), nitrate (NO3), and ortho-phosphate (PO4) ions individually and in combination using a fractional factorial design divided into 4 blocks. High concentrations of Ca and Mg, singly or in combination, increased survival of P. multocida organisms (P < 0.001). We developed a survival index to predict whether or not specific ponds could be "problem" or "nonproblem" avian cholera sites based on concentrations of these ions in the water.

  12. Energy efficient reconcentration of diluted human urine using ion exchange membranes in bioelectrochemical systems.

    PubMed

    Tice, Ryan C; Kim, Younggy

    2014-11-01

    Nutrients can be recovered from source separated human urine; however, nutrient reconcentration (i.e., volume reduction of collected urine) requires energy-intensive treatment processes, making it practically difficult to utilize human urine. In this study, energy-efficient nutrient reconcentration was demonstrated using ion exchange membranes (IEMs) in a microbial electrolysis cell (MEC) where substrate oxidation at the MEC anode provides energy for the separation of nutrient ions (e.g., NH4(+), HPO4(2-)). The rate of nutrient separation was magnified with increasing number of IEM pairs and electric voltage application (Eap). Ammonia and phosphate were reconcentrated from diluted human urine by a factor of up to 4.5 and 3.0, respectively (Eap = 1.2 V; 3-IEM pairs). The concentrating factor increased with increasing degrees of volume reduction, but it remained stationary when the volume ratio between the diluate (urine solution that is diluted in the IEM stack) and concentrate (urine solution that is reconcentrated) was 6 or greater. The energy requirement normalized by the mass of nutrient reconcentrated was 6.48 MJ/kg-N (1.80 kWh/kg-N) and 117.6 MJ/kg-P (32.7 kWh/kg-P). In addition to nutrient separation, the examined MEC reactor with three IEM pairs showed 54% removal of COD (chemical oxygen demand) in 47-hr batch operation. The high sulfate concentration in human urine resulted in substantial growth of both of acetate-oxidizing and H2-oxidizing sulfate reducing bacteria, greatly diminishing the energy recovery and Coulombic efficiency. However, the high microbial activity of sulfate reducing bacteria hardly affected the rate of nutrient reconcentration. With the capability to reconcentrate nutrients at a minimal energy consumption and simultaneous COD removal, the examined bioelectrochemical treatment method with an IEM application has a potential for practical nutrient recovery and sustainable treatment of source-separated human urine.

  13. Aluminum-Cycle Ion Exchange Process for Hardness Removal: A New Approach for Sustainable Softening.

    PubMed

    Li, Jinze; Koner, Suman; German, Michael; SenGupta, Arup K

    2016-11-01

    From a sustainability viewpoint, sodium exchange softening, although used widely, is under scrutiny due to its production of excess Na-laden spent regenerant and subsequent discharge to the environment. Many arid regions are introducing regulations disallowing dumping of concentrated sodium salts, the residuals from popular Na-exchange softening. The sodium content of the softened water is, also, always higher than in the feed, which poses a dietary health concern when used for drinking or cooking. An efficient, easy-to-operate hardness removal process with reduced sodium in both the treated water and in the spent regenerant is an unmet global need. Use of a cation exchange resin in Al(3+)-form for hardness removal, that is, exchange of divalent Ca(2+) or Mg(2+) with trivalent Al(3+), is counterintuitive, and this is particularly so, because the aluminum ion to be exchanged has higher affinity than calcium. Nevertheless, ion exchange accompanied by precipitation of aluminum hydroxide allows progress of the cation exchange reaction leading to hardness removal. Experimental results demonstrated that calcium can be consistently removed for multiple cycles using a stoichiometric amount of AlCl3 as the regenerant. The process essentially operates at the maximum possible thermodynamic efficiency: removal of one equivalent of Ca(2+) corresponds to use of one equivalent of Al(3+) as a regenerant. During the Al-cycle process there is no increase in Na(+) concentration and partial reduction in the total dissolved solids (TDS) of the treated water. It is noteworthy that the ion-exchange resin used, components of the fixed-bed column and operational protocol are nearly the same as traditional softening processes on Na-cycle. Thus, existing Na-cycle systems can be retrofitted into Al-cycle operation without major difficulty.

  14. Continuous separation of carbohydrates by ion-exchange chromatography

    SciTech Connect

    Wolfgang, J.; Prior, A.; Bart, H.J.; Messenboeck, R.C.; Byers, C.H.

    1997-01-01

    A synthetic mixture of fructose, mannitol and sorbitol was continuously separated by a chromatographic method using a cation-exchange resin (Dowex 50W-X8) in its Ca{sup 2+}-form as the stationary phase. An annular chromatograph (AC) was used to achieve a continuous mode of operation. Distribution and mass transfer coefficients of the three substances as well as bed properties were obtained by batch chromatography. The separation was simulated mathematically in terms of an approximate linear chromatographic theory was applied to the modeling of the behavior of the continuous separations. The influence of rotation rate, column loading, eluent flow rate and feed concentration on the resolution of the individual peaks were investigated.

  15. Production of radioactive Ag ion beams with a chemically selective laser ion source

    NASA Astrophysics Data System (ADS)

    Jading, Y.; Catherall, R.; Jokinen, A.; Jonsson, O. C.; Kugler, E.; Lettry, J.; Ravn, H. L.; Tengblad, O.; Kautzsch, T.; Klöckl, I.; Kratz, K.-L.; Scheerer, F.; Fedoseyev, V. N.; Mishin, V. I.; van Duppen, P.; Wöhr, A.; Walters, W. B.

    1996-04-01

    We have developed a chemically selective laser ion source at the CERN-ISOLDE facility in order to study neutron-rich Ag nuclides. A pulsed laser system with high repetition rate has been used based on high-power copper-vapour pump lasers and dye lasers. With this source significant reductions of the isobaric background has been achieved.

  16. Fabrication 3D buried channel optical waveguide modulators on field-driven ion exchange process

    NASA Astrophysics Data System (ADS)

    Zhou, Zigang; Chen, Wenqiang; Zhu, Li; Li, Jing; Luo, Xiaoying

    2010-10-01

    A high electric field technique was developed to fabricate buried optical waveguide modulator on K9 optical glass. The 80V voltage was applied on the glass to accelerate the field-driven ion exchange process by expeditiously replacing host sodium ions in the glass with silver ions. As a result, the optical loss for optical waveguide modulator was measured using the edge coupling technique with a 0.6328μm He-Ne laser. Loss of 0.20 dB/cm was obtained for channel waveguides of 25μm in depth, relatively low for waveguides of such depth at red wavelength.

  17. Ion-Exchanged Waveguides for Signal Processing Applications - A Novel Electrolytic Process.

    DTIC Science & Technology

    1987-03-07

    1986 . 3] R. K. Lagu and V. Ramaswamy, "Fabrication of Single Mode Glass Waveguide by Electrolytic Release of Silver Ions," Appl. Phys. Lett., 45, pp...Quantum Electron., QE-22, pp. 883-891, 1986 . 7 [111] P. Chludzinski, R. V. Ramaswamy, and T. J. Anderson, "Ion-Fxchange Between Sode-Lime Silicate Glass and...Parameter Relationships for the Design of Planar, Silver Ion-Exchanged Glass Waveguide," IEEE J. Lightwave Tech., LT-4, pp. 176-131, 1986 . [20] R. K. Lagu

  18. Ion exchange with the solar wind for planets with negligible intrinsic magnetic fields

    NASA Technical Reports Server (NTRS)

    Nisbet, J. S.

    1979-01-01

    The exchange of ions between the ionosphere of a planet with negligible intrinsic magnetic field, and the solar wind is examined. It is suggested that a balance exists between the outflow of ionospheric ions at the plasmapause and ions from the solar wind in a restricted region close to the subsolar point. This results in a current system towards the subsolar point on the surface of the ionopause and a toroidal magnetic field. Simple calculations are made of the current and field configuration that might result from the system for conditions similar to those encountered on the Viking 1 and 2 transits of the Mars ionosphere.

  19. Development of a Waste Water Regenerative System - Using Sphagnum Moss Ion-exchange

    NASA Astrophysics Data System (ADS)

    McKeon, M.; Wheeler, R.; Leahy, Jj

    The use of inexpensive, light weight and regenerative systems in an enclosed environment is of great importance to sustained existence in such habitats as the International Space Station, Moon or even Mars. Many systems exist which utilise various synthetic ion exchangers to complete the process of waste water clean-up. These systems do have a very good exchange rate for cations but a very low exchange rate for anions. They also have a maximum capacity before they need regeneration. This research proposes a natural alternative to these synthetic ion-exchangers that utilises one of natures greatest ion-exchangers, that of Sphagnum Moss. Sphagna can be predominantly found in the nutrient poor environment of Raised Bogs, a type of isolated wetland with characteristic low pH and little interaction with the surrounding water table. All nutrients come from precipitation. The sphagna have developed as the bog's sponges, soaking up all available nutrients (both cation & anion) from the precipitation and eventually distributing them to the surrounding flora and fauna, through the water. The goal of this research is to use this ability in the processing of waste water from systems similar to isolated microgravity environments, to produce clean water for reuse in these environments. The nutrients taken up by the sphagna will also be utilised as a growth medium for cultivar growth, such as those selected for hydroponics' systems.

  20. Ion-exchange of monovalent and bivalent cations with NaA zeolite membranes : a molecular dynamics study

    NASA Astrophysics Data System (ADS)

    Murad, S.; Jia, W.; Krishnamurthy, M.

    2004-01-01

    Molecular simulations using the method of molecular dynamics have been carried out to study the dynamics and energetics of ion exchanges between monovalent and bivalent cations in supercritical and subcritical (liquid) electrolyte solutions (here Li+, and Ca++ in aqueous solutions of LiCl and CaCl2) and an ion exchange membrane (NaA zeolite) using direct simulations of up to a nanosecond or more. NaA zeolites are widely used in many commercial ion-exchange processes including detergents. Results show that with appropriate driving forces, such ion exchange processes can be clearly witnessed and investigated using molecular simulations at these timescales, especially for supercritical solutions. An attempt is made to understand the phenomenon of ion exchange at the molecular level. Results have shown that the ion-exchange process is primarily energetically driven and entropic forces do not appear to be playing a significant role in the exchanges observed. For supercritical LiCl solutions, small differences were found between the energy of the Li+ inside and outside the membrane. In contrast, for Na+ there was a considerable energetic advantage in being outside the membrane, making the overall exchange process energetically favourable. In subcritical (liquid) LiCl solutions an exchange was found to be more favourable energetically than supercritical solutions. For Ca++ similar trends were observed, except the differences in the energies were much larger (compared to the corresponding Li+ exchanges), making them more energetically efficient, as has also been observed experimentally. In addition to clarifying the molecular basis for these exchanges, simulations can also potentially be very useful to determine the behaviour (e.g. state dependence, etc.) of hydrodynamic parameters commonly used to characterize ion-exchange processes at a fundamental molecular level, and to determine if the hydrodynamic equations used for ion-exchange processes are applicable to nano

  1. High-resolution determination of {sup 147}Pm in urine using dynamic ion-exchange chromatography

    SciTech Connect

    Elchuk, S.; Lucy, C.A.; Burns, K.I.

    1992-10-15

    Ion exchange preconcentration followed by HPLC purification prior to scintillation counting was used to measure the concentration of {sup 147}Pm in urine. the detection limit for this method was found to be 0.1 Bq (3 fg) of {sup 147}Pm in 500 ml of urine.

  2. Synthesis of Anomeric Methyl Fructofuranosides and Their Separation on an Ion-Exchange Resin

    ERIC Educational Resources Information Center

    Nurminen, Erkki; Poijarvi, Paivi; Koskua, Katja; Hovinen, Jari

    2007-01-01

    Treatment of d-fructose with methanol in the presence of acid as a catalyst gives a mixture of methyl-[beta]-d-fructopyranoside, methyl-[alpha]-D-fructofuranoside, and methyl-[beta]-d-fructofuranoside, which were separated on an ion exchange column and characterized polarimetrically.

  3. Advanced Ion Exchange Softening. Training Module 2.212.4.77.

    ERIC Educational Resources Information Center

    McMullen, L. D.

    This document is an instructional module package prepared in objective form for use by an instructor familiar with the operation of an ion exchange softening system. It includes objectives, an instructor guide, student handouts and transparency masters. This is the third level of a three module series. This module considers the theory of ion…

  4. Basic Ion Exchange Softening. Training Module 2.210.2.77.

    ERIC Educational Resources Information Center

    McMullen, L. D.

    This document is an instructional module package prepared in objective form for use by an instructor familiar with ion exchange softening. It includes objectives, an instructor guide, student handouts, and transparency masters. This is the first level of a three module series. The module considers the principles, components, operation,…

  5. Intermediate Ion Exchange Softening. Training Module 2.211.3.77.

    ERIC Educational Resources Information Center

    McMullen, L. D.

    This document is an instructional module package prepared in objective form for use by an instructor familiar with the operation of an ion exchange softening system. It includes objectives, an instructor guide, student handouts, and transparency masters. This is the second level of a three module series. The module considers operation and…

  6. Controlled transdermal delivery of leuprorelin by pulsed iontophoresis and ion-exchange fiber.

    PubMed

    Malinovskaja, Kristina; Laaksonen, Timo; Hirvonen, Jouni

    2014-11-01

    Poor transport efficacy and issues related to biological variation are major concerns in the development of novel iontophoretic devices for the transdermal delivery of therapeutic peptides. The objective of this study was to examine the impact of constant and pulsed current on the transport of nonapeptide leuprorelin acetate across porcine epidermis. Also, the potential of drug delivery system combining iontophoresis and ion-exchange fibers as drug matrices for the delivery of the same peptide was tested. The present study demonstrated the benefit of pulsed current (Tn=2.59×10(-4)) over constant current (Tn=1.7×10(-4)) in terms of more efficient transdermal peptide transport. An increase in the delivery of electroosmotic marker by pulsed current was due to the combined effect of more pronounced electroosmotic transport and reduced inhibition of passive transport. We also showed a promising approach using ion-exchange fibers for controlling the release and iontophoretic transdermal delivery of peptides. Positively charged leuprorelin acetate was bound to the ion-exchange groups of cation-exchange fibers until it was gradually released by mobile counter ions in the external solution. Transdermal flux from acrylic acid grafted Smopex®-102 fibers remained higher (Jss=0.71μg/hcm(2)) than from sulfonic acid grafted Smopex®-101 fibers (Jss=0.31μg/hcm(2)) due to better drug release.

  7. Recycling asymmetric hydrogenation catalysts by their immobilization onto ion-exchange resins.

    PubMed

    Barbaro, Pierluigi

    2006-07-24

    Ion-exchange resins can be used as supports for the preparation of single-site, heterogenised asymmetric hydrogenation catalysts. The immobilised catalysts obtained can be efficiently and conveniently recovered and recycled. This article reviews the significant contributions in the field including the main concepts behind the design and the applications of this type of catalyst.

  8. HIGH ASPECT RATIO ION EXCHANGE RESIN BED - HYDRAULIC RESULTS FOR SPERICAL RESIN BEADS

    SciTech Connect

    Duignan, M; Charles Nash, C; Timothy Punch, T

    2007-09-27

    A principal role of the DOE Savannah River Site is to safely dispose of a large volume of liquid nuclear waste held in many storage tanks. An in-tank ion exchange unit is being considered for cesium removal to accelerate waste processing. This unit is planned to have a relatively high bed height to diameter ratio (10:1). Complicating the design is the need to cool the ion exchange media; therefore, the ion exchange column will have a central cooling core making the flow path annular. To separate cesium from waste the media being considered is made of resorcinol formaldehyde resin deposited on spherical plastic beads and is a substitute for a previously tested resin made of crystalline silicotitanate. This spherical media not only has an advantage of being mechanically robust, but, unlike its predecessor, it is also reusable, that is, loaded cesium can be removed through elution and regeneration. Resin regeneration leads to more efficient operation and less spent resin waste, but its hydraulic performance in the planned ion exchange column was unknown. Moreover, the recycling process of this spherical resorcinol formaldehyde causes its volume to significantly shrink and swell. To determine the spherical media's hydraulic demand a linearly scaled column was designed and tested. The waste simulant used was prototypic of the wastes' viscosity and density. This paper discusses the hydraulic performance of the media that will be used to assist in the design of a full-scale unit.

  9. Catalytic activity of rhodium complex immobilized on AN-31 ion exchanger

    SciTech Connect

    Parshikova, G.N.; Korneva, L.I.; Kononov, Yu.S.

    1995-08-10

    Immobilized platinum-metal complexes are of interest as heterogeneous catalysts. Ion-exchange resins may be used as supports for catalytically active complexes. However, immobilized metal complexes are often unstable, are washed out from supports, and are lost with reaction products. Secure immobilization of metal complexes on supports is possible, for example, via coordination of the central metal by electron-donor groups of the support. This is the case when platinum metals are sorbed from solutions by nitrogen-containing ion exchangers. Complexes thus immobilized have high catalytic activity. Previously the authors demonstrated that rhodium(III) is sorbed from solutions containing rhodium aqua-chloro complexes as stable complexes with AN-31. These complexes were not desorbed with 10 M hydrochloric acid. Stable amino complexes of transition metals sorbed on ion exchangers are known to be active in decomposition of hydrogen peroxide. In this work, the authors have studied catalytic properties of rhodium complex with the ion exchanger under atmospheric pressure at 25-80{degrees}C.

  10. ARSENIC REMOVAL FROM DRINKING WATER BY ION EXCHANGE AND ACTIVATED ALUMINA PLANTS

    EPA Science Inventory

    This report documents a long term performance study of two ion exchange (IE) and two activated alumina (AA) treatment plants to remove arsenic from drinking water. Performance information was collected on these systems that are located in the northeast for one full year. The stud...

  11. Separation and characterisation of beta2-microglobulin folding conformers by ion-exchange liquid chromatography and ion-exchange liquid chromatography-mass spectrometry.

    PubMed

    Bertoletti, Laura; Regazzoni, Luca; Aldini, Giancarlo; Colombo, Raffaella; Abballe, Franco; Caccialanza, Gabriele; De Lorenzi, Ersilia

    2013-04-10

    In this work we present for the first time the use of ion-exchange liquid chromatography to separate the native form and a partially structured intermediate of the folding of the amyloidogenic protein beta2-microglobulin. Using a strong anion-exchange column that accounts for the differences in charge exposure of the two conformers, a LC-UV method is initially optimised in terms of mobile phase pH, composition and temperature. The preferred mobile phase conditions that afford useful information were found to be 35 mM ammonium formate, pH 7.4 at 25°C. The dynamic equilibrium of the two species is demonstrated upon increasing the concentration of acetonitrile in the protein sample. Then, the chromatographic method is transferred to MS detection and the respective charge state distributions of the separated conformers are identified. The LC-MS results demonstrate that one of the conformers is partially unfolded, compared with the native and more compact species. The correspondence with previous results obtained in free solution by capillary electrophoresis suggest that strong ion exchange LC-MS does not alter beta2-microglobulin conformation and maintains the dynamic equilibrium already observed between the native protein and its folding intermediate.

  12. Fractionation of whey proteins with high-capacity superparamagnetic ion-exchangers.

    PubMed

    Heebøll-Nielsen, Anders; Justesen, Sune F L; Thomas, Owen R T

    2004-09-30

    In this study we describe the design, preparation and testing of superparamagnetic anion-exchangers, and their use together with cation-exchangers in the fractionation of bovine whey proteins as a model study for high-gradient magnetic fishing. Adsorbents prepared by attachment of trimethyl amine to particles activated in sequential reactions with allyl bromide and N-bromosuccinimide yielded a maximum bovine serum albumin binding capacity of 156 mg g(-1) combined with a dissociation constant of 0.60 microM, whereas ion-exchangers created by linking polyethylene imine through superficial aldehydes bound up to 337 mg g(-1) with a dissociation constant of 0.042 microM. The latter anion-exchanger was selected for studies of whey protein fractionation. In these, crude bovine whey was treated with a superparamagnetic cation-exchanger to adsorb basic protein species, and the supernatant arising from this treatment was then contacted with the anion-exchanger. For both adsorbent classes of ion-exchanger, desorption selectivity was subsequently studied by sequentially increasing the concentration of NaCl in the elution buffer. In the initial cation-exchange step quantitative removal of lactoferrin (LF) and lactoperoxidase (LPO) was achieved with some simultaneous binding of immunoglobulins (Ig). The immunoglobulins were separated from the other two proteins by desorbing with a low concentration of NaCl (< or = 0.4 M), whereas lactoferrin and lactoperoxidase were co-eluted in significantly purer form, e.g. lactoperoxidase was purified 28-fold over the starting material, when the NaCl concentration was increased to 0.4-1 M. The anion-exchanger adsorbed beta-lactoglobulin (beta-LG) selectively allowing separation from the remaining protein.

  13. Conversion of ion-exchange resins, catalysts and sludges to glass with optional noble metal recovery using the GMODS process

    SciTech Connect

    Forsberg, C.W.; Beahm, E.C.

    1996-11-01

    Chemical processing and cleanup of waste streams (air and water) typically result in products, clean air, clean water, and concentrated hazardous residues (ion exchange resins, catalysts, sludges, etc.). Typically, these streams contain significant quantities of complex organics. For disposal, it is desirable to destroy the organics and immobilize any heavy metals or radioactive components into stable waste forms. If there are noble metals in the residues, it is desirable to recover these for reuse. The Glass Material Oxidation and Dissolution System (GMODS) is a new process that directly converts radioactive and hazardous chemical wastes to borosilicate glass. GMODS oxidizes organics with the residue converted to glass; converts metals, ceramics, and amorphous solids to glass; converts halides (eg chlorides) to borosilicate glass and a secondary sodium halide stream; and recovers noble metals. GMODS has been demonstrated on a small laboratory scale (hundreds of grams), and the equipment needed for larger masses has been identified.

  14. Atomic hydrogen escape rate due to charge exchange with hot plasmaspheric ions

    NASA Technical Reports Server (NTRS)

    Maher, L. J.; Tinsley, B. A.

    1977-01-01

    Data on ion and electron temperatures and concentrations to several thousand kilometers of altitude were obtained from the Atmosphere Explorer C satellite for 1974 and to 850 km from Arecibo incoherent scatter radar measurements. These data were used to normalize diffusive equilibrium profiles. From these profiles and by using the neutral atmospheric model of Jacchia (1971) and a new hydrogen model, the charge-exchange-induced neutral hydrogen escape fluxes for equatorial and middle latitudes were calculated. The data confirm earlier estimates that the charge exchange loss is more important than Jeans escape for the earth. It is also found that inside the plasmapause this charge exchange process with hot plasmapheric ions is the major production and loss process for the satellite population in the hydrogen geocorona.

  15. Removal of chromium from electroplating industry effluents by ion exchange resins.

    PubMed

    Cavaco, Sofia A; Fernandes, Sandra; Quina, Margarida M; Ferreira, Licínio M

    2007-06-18

    Effluent discharged from the chromium electroplating industry contains a large number of metals, including chromium, copper, nickel, zinc, manganese and lead. The ion exchange process is an alternative technique for application in the treatment of industrial wastewater containing heavy metals and indeed it has proven to be very promising in the removal and recovery of valuable species. The main objective of the present work is to evaluate the performance of commercial ion exchange resins for removing chromium trivalent from industrial effluents, and for this purpose two resins were tested: a chelating exchange resin (Diaion CR11) and a weak cationic resin (Amberlite IRC86). In order to evaluate the sorption capacity of the resins some equilibrium experiments were carried out, being the temperature and pH the main variables considered. The chromium solutions employed in the experiments were synthetic solutions and industrial effluents. In addition, a transient test was also performed as an attempt to understand the kinetic behaviour of the process.

  16. Quantitative determination of Mg in Al-alloys by ion-exchange TLC

    SciTech Connect

    Petrovic, M.; Kastelan-Macan, M. . Lab. for Analytical Chemistry); Turina, S.; Ivankovic, V. . Faculty of Mechanical Engineering and Naval Architecture)

    1993-01-01

    Analytical procedure for the quantitative determination of Mg in Al-alloys using ion-exchange thin layer chromatography is described. Chromatographic plates were coated with Amberlite IRP-69 (strong-acid cation exchanger in H[sup +]-form) mixed in different ratios with microcrystalline cellulose. Solutions of HCl and HNO[sub 3] respectively, in the concentration range from 0.5-2.0 mol dm[sup [minus]3] were used as developers. Chromatograms were visualized by spraying with ethanolic solution of 8-hydroxyquinoline and spots were scanned using Camag Turner Fluorometer 111. The optical separation was obtained on TLC plates containing 23% of ion-exchanger (particle size < 60 [mu]m) and by eluting with 1.25 M HCl. R[sub F] (Al) = 0.12, R[sub F](Mg) = 0.41.

  17. Competitive migration behaviors of multiple ions and their impacts on ion-exchange resin packed microbial desalination cell.

    PubMed

    Zuo, Kuichang; Yuan, Lulu; Wei, Jincheng; Liang, Peng; Huang, Xia

    2013-10-01

    Mixed ion-exchange resins packed microbial desalination cell (R-MDC) could stabilize the internal resistance, however, the impacts of multiple ions on R-MDC performance was unclear. This study investigated the desalination performance, multiple ions migration behaviors and their impacts on R-MDCs fed with salt solution containing multiple anions and cations. Results showed that R-MDC removed multiple anions better than multiple cations with desalination efficiency of 99% (effluent conductivity <0.05 ms/cm) at hydraulic retention time of 50 h. Competitive migration order was SO4(2-)>NO3(-)>Cl(-) for anions and Ca(2+)≈Mg(2+)>NH4(+)>Na(+) for cations, jointly affected by both their molar conductivity and exchange selectivity on resins. After long-term operation, the existence of higher concentration Ca(2+) and Mg(2+) caused the electric conductivity of mixed resins decrease and scaling on the surface of cation-exchange membrane adjoined with cathode chamber, suggesting that R-MDC would be more suitable for desalination of water with lower hardness.

  18. Ion exchange membranes as novel passive sampling material for organic ions: application for the determination of freely dissolved concentrations.

    PubMed

    Oemisch, Luise; Goss, Kai-Uwe; Endo, Satoshi

    2014-11-28

    Many studies in pharmacology, toxicology and environmental science require a method for determining the freely dissolved concentration of a target substance. A recently developed tool for this purpose is equilibrium passive sampling with polymeric materials. However, this method has rarely been applied to ionic organic substances, primarily due to limited availability of convenient sorption materials. This study introduces ion exchange membranes (IEMs) as a novel passive sampling material for organic ions. The partitioning of 4-ethylbenzene-1-sulfonate, 2,4-dichlorophenoxyacetic acid and pentachlorophenol to one anion exchange membrane (FAS) and of difenzoquat, nicotine and verapamil to one cation exchange membrane (FKS) was investigated. All test substances exhibited a sufficiently high affinity for the respective IEM with logarithmic IEM-water partition coefficients >2.3. Sorption equilibrium was established quickly, within several hours for the FAS membrane and within 1-3 days for the FKS membrane. For permanently charged substances the partitioning to the IEMs was independent of pH, but was influenced by the salt composition of the test solution. For all test substances sorption to IEM was dependent on the substance concentration. Bovine serum albumin-water partition coefficients determined by passive sampling with IEMs agree well with those determined by the conventional dialysis method. The results of this study indicate that IEMs exhibit the potential to measure freely dissolved concentrations of organic ions in a simple and time-saving manner.

  19. Preconceptual design for separation of plutonium and gallium by ion exchange

    SciTech Connect

    DeMuth, S.F.

    1997-09-30

    The disposition of plutonium from decommissioned nuclear weapons, by incorporation into commercial UO{sub 2}-based nuclear reactor fuel, is a viable means to reduce the potential for theft of excess plutonium. This fuel, which would be a combination of plutonium oxide and uranium oxide, is referred to as a mixed oxide (MOX). Following power generation in commercial reactors with this fuel, the remaining plutonium would become mixed with highly radioactive fission products in a spent fuel assembly. The radioactivity, complex chemical composition, and large size of this spent fuel assembly, would make theft difficult with elaborate chemical processing required for plutonium recovery. In fabricating the MOX fuel, it is important to maintain current commercial fuel purity specifications. While impurities from the weapons plutonium may or may not have a detrimental affect on the fuel fabrication or fuel/cladding performance, certifying the effect as insignificant could be more costly than purification. Two primary concerns have been raised with regard to the gallium impurity: (1) gallium vaporization during fuel sintering may adversely affect the MOX fuel fabrication process, and (2) gallium vaporization during reactor operation may adversely affect the fuel cladding performance. Consequently, processes for the separation of plutonium from gallium are currently being developed and/or designed. In particular, two separation processes are being considered: (1) a developmental, potentially lower cost and lower waste, thermal vaporization process following PuO{sub 2} powder preparation, and (2) an off-the-shelf, potentially higher cost and higher waste, aqueous-based ion exchange (IX) process. While it is planned to use the thermal vaporization process should its development prove successful, IX has been recommended as a backup process. This report presents a preconceptual design with material balances for separation of plutonium from gallium by IX.

  20. Molecular secondary ion mass spectrometry: New dimensions in chemical characterization

    NASA Astrophysics Data System (ADS)

    Colton, Richard J.; Campana, Joseph E.; Kidwell, David A.; Ross, Mark M.; Wyatt, Jeffrey R.

    1985-04-01

    Secondary ion mass spectrometry (SIMS) has become a diverse tool for the study of many substances other than metals and semiconductors. This paper discusses the emission of polyatomic and molecular ions from surfaces that contain various inorganic and organic compounds including polymers and biomolecules. The mass and abundance distribution of cluster ions emitted from various solids — Van der Waals, metallic, ionic and covalent — are compared. Trends in the emission patterns are discussed in terms of a recombination or direct emission mechanism. The emission of molecular ions is also discussed with respect to the method of ionization and the various sample preparation and matrix-assisted procedures used. The matrices include various solid-state and liquid matrices such as ammonium chloride, charcoal, glycerol and gallium. Various chemical derivatization procedures have been developed to enhance the sensitivity of molecular SIMS and to detect selectively components in mixtures. The procedures are demonstrated for the low-level detection of airborne contaminants from paints, for the analysis of drugs in biological fluids, and for the sequencing of biomolecules such as peptides and sugars. The emission of characteristic fragment ions from the surfaces of polymers is also described for thick, insulating films.