WorldWideScience

Sample records for metal ion separation

  1. Separation of metal ions from aqueous solutions

    Science.gov (United States)

    Almon, Amy C.

    1994-01-01

    A process and apparatus for quantitatively and selectively separating metal ions from mixtures thereof in aqueous solution. The apparatus includes, in combination, a horizontal electrochemical flow cell containing flow bulk electrolyte solution and an aqueous, metal ion-containing solution, the cell containing a metal mesh working electrode, a counter electrode positioned downstream from the working electrode, an independent variable power supply/potentiostat positioned outside of the flow cell and connected to the electrodes, and optionally a detector such as a chromatographic detector, positioned outside the flow cell. This apparatus and its operation has significant application where trace amounts of metal ions are to be separated.

  2. Metal ion separations using reactive membranes

    International Nuclear Information System (INIS)

    Way, J.D.

    1993-01-01

    A membrane is a barrier between two phases. If one component of a mixture moves through the membrane faster than another mixture component, a separation can be accomplished. Membranes are used commercially for many applications including gas separations, water purification, particle filtration, and macromolecule separations (Abelson). There are two points to note concerning this definition. First, a membrane is defined based on its function, not the material used to make the membrane. Secondly, a membrane separation is a rate process. The separation is accomplished by a driving force, not by equilibrium between phases. Liquids that are immiscible with the feed and product streams can also be used as membrane materials. Different solutes will have different solubilities and diffusion coefficients in a liquid. The product of the diffusivity and the solubility is known as the permeability coefficient, which is proportional to the solute flux. Differences in permeability coefficient will produce a separation between solutes at constant driving force. Because the diffusion coefficients in liquids are typically orders of magnitude higher than in polymers, a larger flux can be obtained. Further enhancements can be accomplished by adding a nonvolatile complexation agent to the liquid membrane. One can then have either coupled or facilitated transport of metal ions through a liquid membrane. The author describes two implementations of this concept, one involving a liquid membrane supported on a microporous membrane, and the other an emulsion liquid membrane, where separation occurs to internal receiving phases. Applications and costing studies for this technology are reviewed, and a brief summary of some of the problems with liquid membranes is presented

  3. Progress in metal ion separation and preconcentration : an overview.

    Energy Technology Data Exchange (ETDEWEB)

    Bond, A. H.

    1998-05-19

    A brief historical perspective covering the most mature chemically-based metal ion separation methods is presented, as is a summary of the recommendations made in the 1987 National Research Council (NRC) report entitled ''Separation and Purification: Critical Needs and Opportunities''. A review of Progress in Metal Ion Separation and Preconcentration shows that advances are occurring in each area of need cited by the NRC. Following an explanation of the objectives and general organization of this book, the contents of each chapter are briefly summarized and some future research opportunities in metal ion separations are presented.

  4. Progress in metal ion separation and preconcentration: an overview

    International Nuclear Information System (INIS)

    Bond, A. H.

    1998-01-01

    A brief historical perspective covering the most mature chemically-based metal ion separation methods is presented, as is a summary of the recommendations made in the 1987 National Research Council (NRC) report entitled ''Separation and Purification: Critical Needs and Opportunities''. A review of Progress in Metal Ion Separation and Preconcentration shows that advances are occurring in each area of need cited by the NRC. Following an explanation of the objectives and general organization of this book, the contents of each chapter are briefly summarized and some future research opportunities in metal ion separations are presented

  5. New Proton-Ionizable, Calixarene-Based Ligands for Selective Metal Ion Separations

    Energy Technology Data Exchange (ETDEWEB)

    Bartsch, Richard A.

    2012-06-04

    The project objective was the discovery of new ligands for performing metal ion separations. The research effort entailed the preparation of new metal ion complexing agents and polymers and their evaluation in metal ion separation processes of solvent extraction, synthetic liquid membrane transport, and sorption. Structural variations in acyclic, cyclic, and bicyclic organic ligands were used to probe their influence upon the efficiency and selectivity with which metal ion separations can be performed. A unifying feature of the ligand structures is the presence of one (or more) side arm with a pendent acidic function. When a metal ion is complexed within the central cavity of the ligand, ionization of the side arm(s) produces the requisite anion(s) for formation of an overall electroneutral complex. This markedly enhances extraction/transport efficiency for separations in which movement of aqueous phase anions of chloride, nitrate, or sulfate into an organic medium would be required. Through systematic structural variations, new ligands have been developed for efficient and selective separations of monovalent metal ions (e.g., alkali metal, silver, and thallium cations) and of divalent metal ion species (e.g., alkaline earth metal, lead, and mercury cations). Research results obtained in these fundamental investigations provide important insight for the design and development of ligands suitable for practical metal ion separation applications.

  6. Preorganized and Immobilized Ligands for Metal Ion Separations

    Energy Technology Data Exchange (ETDEWEB)

    Paine, Robert T. [Univ. of New Mexico, Albuquerque, NM (United States)

    2015-07-01

    The research project, in the period 2003-2015, was focused on the discovery of fundamental new principles in f-element ion coordination chemistry and the application of the new knowledge to the development of advanced detection/separations reagents and methods for these ions. The findings relate to the Nation's efforts to safely and efficiently process nuclear materials. In addition, the project provided training for young scientists needed to maintain the Nation's preeminence in nuclear science.

  7. Solvent extraction, membranes, and ion exchange in hydrometallurgical dilute metals separation

    International Nuclear Information System (INIS)

    Tavlarides, L.L.; Bae, J.H.; Lee, C.K.

    1987-01-01

    The separation methods which are used in the hydro-metallurgical field are reviewed and compared. Some processes in solvent extraction in use for recovery of crucial metals which are important to the US defense and economy are presented. Various commercial extractants are reviewed and categorized. Other methods such as liquid membranes and ions exchange resins used for dilute metal ions separation are summarized. These methods are compared with solvent extraction. Problems to overcome in the future development of these separation methods are also identified and discussed in this paper

  8. A simple alkali-metal and noble gas ion source for SIMS equipments with mass separation of the primary ions

    International Nuclear Information System (INIS)

    Duesterhoeft, H.; Pippig, R.

    1986-01-01

    An alkali-metal ion source working without a store of alkali-metals is described. The alkali-metal ions are produced by evaporation of alkali salts and ionization in a low-voltage arc discharge stabilized with a noble gas plasma or in the case of small alkali-metal ion currents on the base of the well known thermic ionization at a hot tungsten wire. The source is very simple in construction and produces a stable ion current of 0.3 μA for more than 100 h. It is possible to change the ion species in a short time. This source is applicable to all SIMS equipments using mass separation for primary ions. (author)

  9. Polymer-supported reagents with enhanced metal ion recognition: Application to separations science

    International Nuclear Information System (INIS)

    Alexandratos, S.D.

    1993-01-01

    The design and development of polymer-supported reagents with ever-increasing specificities for targeted metal ions remains an important areas of research. The need for efficient separation schemes for both ions and molecules has been outlined in a report by the National Research Council (King) and will gain increased emphasis as environmental restoration is pursued. Polymer-supported reagents are unique in their ability to be applied in an environmentally benign manner to a host of challenges. Such reagents, in the form of beads, can be applied to continuous separation processes ranging from the removal of metal ions in water to the recovery of medicinal drugs produced through biotechnological means. The application of polymer-supported reagents to metal ion separations still requires developing a fundamental understanding of ligand-metal interactions, the role of the polymer in those interactions, and the methods of synthesizing such polymeric reagents in a readily applicable form. Ion exchange resins with sulfonic acid ligands are the prototypical polymer-supported reagents, and their properties have been exhaustively studied (Helfferich). The high acidity of the sulfonic acid group, however, precludes much selectivity, and it displays a very limited range of reaction free energy values with different metal ions (Boyd et al.). The carboxylic acid ligand, present in the acrylate resins, is more selective, though its weak acidity requires relatively high pH solutions for it to be effective. Research has thus been focused on the preparation of polymer-supported reagents with high levels of specificity for targeted metal ions

  10. Column Extraction and Separation of Some Metal Ions by Diethylenetriamine Polysiloxane Immobilized Ligand System

    Directory of Open Access Journals (Sweden)

    Nizam M. El-Ashgar

    2008-01-01

    Full Text Available An extraction chromatographic solid porous polysiloxane functionalized by chelating diethylenetriamine ligand of the general formula P-(CH23-NH(CH22NH(CH22NH2, (Where P represents [Si-O]n siloxane network has been evaluated for the separation of Co(II, Ni(II and Cu(II from aqueous solutions. The chromatographic parameters of the separation method have been optimized. The ligand system retained Co(II, Cu(II and Zn(II effectively when used as a metal ion extractant by controlling the pH value. The ligand system also shows a good separation of a mixture of metal ions Co(II, Ni(II and Cu(II when used as chromatographic stationary phase. The optimum separation pH values were 4.5, 4 for Co(II and Ni(II respectively, while a solution of 0.1 M HNO3 was used to elute Cu(II. Metal ions were also preconcentrated at pH 5.5. The chemisorbed metal ions were regenerated from the solid extractant using 0.5 M HCl.

  11. Development of a four-zone carousel process packed with metal ion-imprinted polymer for continuous separation of copper ions from manganese ions, cobalt ions, and the constituent metal ions of the buffer solution used as eluent.

    Science.gov (United States)

    Jo, Se-Hee; Park, Chanhun; Yi, Sung Chul; Kim, Dukjoon; Mun, Sungyong

    2011-08-19

    A three-zone carousel process, in which Cu(II)-imprinted polymer (Cu-MIP) and a buffer solution were employed as adsorbent and eluent respectively, has been developed previously for continuous separation of Cu²⁺ (product) from Mn²⁺ and Co²⁺ (impurities). Although this process was reported to be successful in the aforementioned separation task, the way of using a buffer solution as eluent made it inevitable that the product stream included the buffer-related metal ions (i.e., the constituent metal ions of the buffer solution) as well as copper ions. For a more perfect recovery of copper ions, it would be necessary to improve the previous carousel process such that it can remove the buffer-related metal ions from copper ions while maintaining the previous function of separating copper ions from the other 2 impure heavy-metal ions. This improvement was made in this study by proposing a four-zone carousel process based on the following strategy: (1) the addition of one more zone for performing the two-step re-equilibration tasks and (2) the use of water as the eluent of the washing step in the separation zone. The operating conditions of such a proposed process were determined on the basis of the data from a series of single-column experiments. Under the determined operating conditions, 3 runs of carousel experiments were carried out. The results of these experiments revealed that the feed-loading time was a key parameter affecting the performance of the proposed process. Consequently, the continuous separation of copper ions from both the impure heavy-metal ions and the buffer-related metal ions could be achieved with a purity of 91.9% and a yield of 92.8% by using the proposed carousel process based on a properly chosen feed-loading time. Copyright © 2011 Elsevier B.V. All rights reserved.

  12. Separation of some metal ions using coupled transport supported liquid membranes

    International Nuclear Information System (INIS)

    Chaudhary, M.A.

    1993-01-01

    Liquid membrane extraction processes has become very popular due to their superiority in many ways over other separation techniques. In coupled transport membranes the metal ions can be transported across the membrane against their concentration gradient under the influence of chemical potential difference. Liquid membranes consisting of a carrier-cum-diluent, supported in microporous polymeric hydrophobic films have been studied for transport of metal ions like U(VI), Cr(VI), Be(II), V(V), Ti(IV), Zn(II), Cd(II), Hf(IV), W(VI), and Co(II). The present paper presents basic data with respect to flux and permeabilities of these metal ions across membranes based on experimental results and theoretical equations, using different carriers and diluents and provides a brief reference to possibility of such membranes for large scale applications. (author)

  13. Automated ion-exchange system for the radiochemical separation of the noble metals

    International Nuclear Information System (INIS)

    Parry, S.J.

    1980-01-01

    Ion-exchange separation is particularly suitable for mechanisation and automated ion exchange has been applied to the activation analysis of biological and environmental samples. In this work a system has been designed for experimental studies, which can be adapted for different modes of operation. The equipment is based on a large-volume sampler for the automatic presentation of 500 ml of liquid to a sampling probe. The sample is delivered to the ion-exchange column by means of a peristaltic pump. The purpose of this work was to automate a procedure for separating the noble metals from irradiated geological samples, for neutron-activation analysis. The process of digesting the rock sample is carried out manually in 30 min and is not suited to unattended operation. The volume of the resulting liquid sample may be 100 ml and so the manual separation step may take as long as 1.25 h per sample. The reason for automating this part of the procedure is to reduce the separation time for a group of five samples and consequently to improve the sensitivity of the analysis for radionuclides with short half-lives. This paper describes the automatic ion-exchange system and the ways in which it can be used. The mode of operation for the separation of the noble metals is given in detail. The reproducibility of the system has been assessed by repeated measurements on a standard reference matte. (author)

  14. Evaluation of complexing agents and column temperature in ion chromatographic separation of alkali metals, alkaline earth metals and transition metals ion

    International Nuclear Information System (INIS)

    Kelkar, Anoop; Pandey, Ashish; Name, Anil B.; Das, D.K.; Behere, P.G.; Mohd Afzal

    2015-01-01

    The aim of ion chromatography method development is the resolution of all metal ions of interests. Resolution can be improved by changing the selectivity. Selectivity in chromatography can be altered by changes in mobile phase (eg eluent type, eluent strength) or through changes in stationary phase. Temperature has been used in altering the selectivity of particularly in reversed phase liquid chromatography and ion exchange chromatography. Present paper describe the retention behaviour of alkali metals, alkaline earth metals and transition metal ions on a silica based carboxylate function group containing analyte column. Alkali metals, alkaline earth metals and transition metal ions were detected by ion conductivity and UV-VIS detectors respectively

  15. Production of intense metallic ion beams in order of isotopic separations

    International Nuclear Information System (INIS)

    Sarrouy, J.L.

    1955-01-01

    We describe an isotope separator with magnetic sector of 60 deg that permits, with a process of neutralization of the space charge, to use efficiently intense ion beams. The sources of realized ions provide ionic debits of 10 mA. This present work deals who to obtain intense ion beams (10 to 15 mA), different processes of ion currents measurement, as well as the study of the phenomenon of space charge neutralization. The second part of this memory will be on the survey and the adaptation on the source of various type of oven permitting to spray and to ionize metals directly. By order of increasing difficulty of vaporization, we reached the chromium. (M.B.) [fr

  16. Column Extraction and Separation of Some Metal Ions by Diethylenetriamine Polysiloxane Immobilized Ligand System

    OpenAIRE

    El-Ashgar, Nizam M.

    2008-01-01

    An extraction chromatographic solid porous polysiloxane functionalized by chelating diethylenetriamine ligand of the general formula P-(CH2)3-NH(CH2)2NH(CH2)2NH2, (Where P represents [Si-O]n siloxane network) has been evaluated for the separation of Co(II), Ni(II) and Cu(II) from aqueous solutions. The chromatographic parameters of the separation method have been optimized. The ligand system retained Co(II), Cu(II) and Zn(II) effectively when used as a metal ion extractant by controlling the...

  17. The effect of magnetite nanoparticles synthesis conditions on their ability to separate heavy metal ions

    Directory of Open Access Journals (Sweden)

    Bobik Magdalena

    2017-06-01

    Full Text Available Magnetite nanoparticles have become a promising material for scientific research. Among numerous technologies of their synthesis, co-precipitation seems to be the most convenient, less time-consuming and cheap method which produces fine and pure iron oxide particles applicable to environmental issues. The aim of the work was to investigate how the co-precipitation synthesis parameters, such as temperature and base volume, influence the magnetite nanoparticles ability to separate heavy metal ions. The synthesis were conducted at nine combinations of different ammonia volumes - 8 cm3, 10 cm3, 15 cm3 and temperatures - 30°C, 60°C, 90°C for each ammonia volume. Iron oxides synthesized at each combination were examined as an adsorbent of seven heavy metals: Cr(VI, Pb(II, Cr(III, Cu(II, Zn(II, Ni(II and Cd(II. The representative sample of magnetite was characterized using XRD, SEM and BET methods. It was observed that more effective sorbent for majority of ions was produced at 30°C using 10 cm3 of ammonia. The characterization of the sample produced at these reaction conditions indicate that pure magnetite with an average crystallite size of 23.2 nm was obtained (XRD, the nanosized crystallites in the sample were agglomerated (SEM and the specific surface area of the aggregates was estimated to be 55.64 m2·g-1 (BET. The general conclusion of the work is the evidence that magnetite nanoparticles have the ability to adsorb heavy metal ions from the aqueous solutions. The effectiveness of the process depends on many factors such as kind of heavy metal ion or the synthesis parameters of the sorbent.

  18. Enhancing glycan isomer separations with metal ions and positive and negative polarity ion mobility spectrometry-mass spectrometry analyses

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Xueyun; Zhang, Xing; Schocker, Nate; Renslow, Ryan S.; Orton, Daniel J.; Khamsi, Jamal; Ashmus, Roger A.; Almeida, Igor C.; Tang, Keqi; Costello, Catherine E; Smith, Richard D.; Michael, Katja; Baker, Erin M.

    2016-09-07

    Glycomics has become an increasingly important field of research since glycans play critical roles in biology processes ranging from molecular recognition and signaling to cellular communication. Glycans often conjugate with other biomolecules such as proteins and lipids, and alter their properties and functions, so understanding the effect glycans have on cellular systems is essential. However the analysis of glycans is extremely difficult due to their complexity and structural diversity (i.e., the number and identity of monomer units, and configuration of their glycosidic linkages and connectivities). In this work, we coupled ion mobility spectrometry with mass spectrometry (IMS-MS) to characterize glycan standards and biologically important isomers of synthetic αGal-containing O-glycans including glycotopes of the protozoan parasite Trypanosoma cruzi, which is the causative agent of Chagas disease. IMS-MS results showed significant differences for the glycan structural isomers when analyzed in positive and negative polarity and complexed with different metal cations. These results suggest specific metal ions or ion polarities could be used to target and baseline separate glycan isomers of interest with IMS-MS.

  19. Investigation of the potential of silica-bonded macrocyclic ligands for separation of metal ions from nuclear waste

    International Nuclear Information System (INIS)

    Camaioni, D.M.; Colton, N.G.; Bruening, R.L.

    1992-01-01

    This report describes the testing of some novel separations materials known as SuperLig trademark materials for their ability to separate efficiently and selectively certain metal ions from a synthetic, nonradioactive nuclear waste solution. The materials, developed and patented by IBC Advanced Technologies, are highly selective macrocyclic ligands that have been covalently bonded to silica gel. The SuperLig trademark materials that were tested are: (1) SuperLig trademark 601 for barium (Ba 2+ ) and strontium (Sr 2+ ) separation, (2) SuperLig trademark 602 for cesium (Cs + ) and rubidium (Rb + ) separation, (3) SuperLig trademark 27 for palladium (Pd 2+ ) separation, and (4) SuperLig trademark II for silver (Ag + ) and ruthenium (Ru 3+ ) separation. Our observations show that the technology for separating metal ions using silica-bonded macrocycles is essentially sound and workable to varying degrees of success that mainly depend on the affinity of the macrocycle for the metal ion of interest. It is expected that ligands will be discovered or synthesized that are amenable to separating metal ions of interest using this technology. Certainly more development, testing, and evaluation is warranted. 3 figs., 11 tabs

  20. Separation and recovery of chromium and vanadium metal ions from waste waters

    International Nuclear Information System (INIS)

    Rothmann, H.; Bauer, G.; Stuhr, A.; Retelsdorf, H-J.

    1987-01-01

    Possibilities of Cr- and V- recovery from waste waters, precipitation of chromate and vanadate ions as insoluble compounds, absorption of Cr and V on solid ion exchange resins, absorption of Cr and V on fluid ion exchangers. Extraction with fluid exchangers: simultaneous extraction of Cr and V with Ion Exchanger Hoe F 1857 to determine the distribution isotherms, separate extraction of Cr in a continuously operating mixer-settler plant, separate extraction of vanadate in a constantly operating mixer-settler plant, test with an extraction column, losses in the organic phase during chromium and vanadium extraction, discussion of the test results and economic considerations

  1. Synthesis and Ion-Exchange Properties of Graphene Th(IV) Phosphate Composite Cation Exchanger: Its Applications in the Selective Separation of Lead Metal Ions.

    Science.gov (United States)

    Rangreez, Tauseef Ahmad; Asiri, Abdullah M; Alhogbi, Basma G; Naushad, Mu

    2017-07-24

    In this study, graphene Th(IV) phosphate was prepared by sol-gel precipitation method. The ion-exchange behavior of this cation-exchanger was studied by investigating properties like ion-exchange capacity for various metal ions, the effect of eluent concentration, elution behavior, and thermal effect on ion-exchange capacity (IEC). Several physicochemical properties as Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) study, thermal studies, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies were also carried out. The material possessed an IEC of 1.56 meq·dry·g -1 of the exchanger and was found to be nano-composite. The selectivity studies showed that the material is selective towards Pb(II) ions. The selectivity of this cation-exchanger was demonstrated in the binary separation of Pb(II) ions from mixture with other metal ions. The recovery was found to be both quantitative and reproducible.

  2. SEPARATION OF Ca AND Fe METAL ION IN SOURCE WATER BY ADSORPTION COLUMN TECHNIC WITH LOCAL ZEOLITE AND ACTIVE CARBON

    Directory of Open Access Journals (Sweden)

    Suyanta Suyanta

    2016-04-01

    Full Text Available This research aims are to separate of Ca and Fe metal ion in source water, with local zeolite and active carbon by adsorption column technic. Efficiency of separation are control by adsorption time and size of zeolite. Method that used was column adsorption with a flow system in which sample is applied to the filtration tube containing zeolite and active carbon. Initial and final concentrations of the samples were analyzed using Atomic Adsorption Spectrophotometer instrument. The results obtained shows that ability adsorption of zeolite to Ca and Fe metal ion are a good. Zeolite 1 (10 mesh can reduce iron concentration until 93.98 % and zeolite 2 (5mesh until 98.88% for 1 – 4 week range time. Whereas reducing of calcium concentration is not good, until 2 week period time adsorption of calcium ion is about 50%.   Keywords: adsorption, zeolite, source water

  3. Iminodiacetic acid functionalised organopolymer monoliths: application to the separation of metal cations by capillary high-performance chelation ion chromatography.

    Science.gov (United States)

    Moyna, Áine; Connolly, Damian; Nesterenko, Ekaterina; Nesterenko, Pavel N; Paull, Brett

    2013-03-01

    Lauryl methacrylate-co-ethylene dimethacrylate monoliths were polymerised within fused silica capillaries and subsequently photo-grafted with varying amounts of glycidyl methacrylate (GMA). The grafted monoliths were then further modified with iminodiacetic acid (IDA), resulting in a range of chelating ion-exchange monoliths of increasing capacity. The IDA functional groups were attached via ring opening of the epoxy group on the poly(GMA) structure. Increasing the amount of attached poly(GMA), via photo-grafting with increasing concentrations of GMA, from 15 to 35%, resulted in a proportional and controlled increase in the complexation capacity of the chelating monoliths. Scanning capacitively coupled contactless conductivity detection (sC(4)D) was used to characterise and verify homogenous distribution of the chelating ligand along the length of the capillaries non-invasively. Chelation ion chromatographic separations of selected transition and heavy metals were carried out, with retention factor data proportional to the concentration of grafted poly(GMA). Average peak efficiencies of close to 5,000 N/m were achieved, with the isocratic separation of Na, Mg(II), Mn(II), Co(II), Cd(II) and Zn(II) possible on a 250-mm-long monolith. Multiple monolithic columns produced to the same recipes gave RSD data for retention factors of ions). The monolithic chelating ion-exchanger was applied to the separation of alkaline earth and transition metal ions spiked in natural and potable waters.

  4. Extended X-ray absorption fine structure investigation of adsorption and separation phenomena of metal ions in organic resin.

    Science.gov (United States)

    Ikeda, Atsushi; Yaita, Tsuyoshi; Okamoto, Yoshihiro; Shiwaku, Hideaki; Suzuki, Shinichi; Suzuki, Tatsuya; Fujii, Yasuhiko

    2007-11-01

    Analytical technique using organic resins has already been well-developed, and its applications are employed in various fields; nevertheless, the chemical phenomena occurring inside the resin remain unclear for the most part. In the present study, we apply EXAFS spectroscopy to elucidate the adsorption and separation phenomena of metal ions by organic resin. That is, the chemical species of trivalent lanthanides (Ln(III)) adsorbed in a tertiary pyridine resin from hydrochloric acid and nitric acid solutions have been determined by EXAFS. The results in HCl solutions suggest that Ln(III) ions are partly dehydrated in the resin phase, enabling the pyridine groups of the resin and chloride ions to coordinate to the Ln(III) ions in their primary coordination sphere. On the other hand, Ln(III) ions are tightly coordinated by several nitrate ions in HNO3 solutions and they keep forming the nitrate complex even in the resin phase. The lighter Ln of Nd tends to form an anionic nitrate complex, [Nd(NO3)4.nH2O]-, in the resin phase, while the middle Ln of Sm exists as a cationic nitrate complex, [Sm(NO3)2.nH2O]+, for the most part. On the basis of these EXAFS results, the adsorption and separation mechanisms of the pyridine resin in HCl solutions are interpreted as the direct coordination of pyridine groups to metal ions, while the mechanisms in HNO3 solutions are mainly dominated by the anion-exchange reaction between the protonated pyridine groups and the anionic nitrate complexes of Ln(III). The obtained results demonstrate that the hydration of metal ions weakens, and instead, other complexations are enhanced in the resin phase.

  5. Separation of uranium and other metals from commercial phosphoric acid by ion-exchange and voltammetric determination of uranium

    International Nuclear Information System (INIS)

    Ferreira, J.B.C.; Carvalho, F.M.S. de; Abrao, A.

    1985-11-01

    The separation of metals from crude commercial phosphoric acid is achieved by simple dilution and percolation through a strong cationic ion exchanger. Uranium, calcium, magnesium, manganese, iron and aluminum are quantitatively fixed by the exchanger and can be detected or analysed after their complete elution with 6 M HCI. Titanium and zirconium are only partially retained. Specially for its separation and determination uranium is retained selectively by the resin from the phosphoric acid-EDTA solution, the column is washed with water and then eluted with hydrochloric acid. Uranium is analyzed by voltametry with the hanging drop mercury electrode. (Author) [pt

  6. Non-destructive separation of metal ions from wastewater containing excess aminopolycarboxylate chelant in solution with an ion-selective immobilized macrocyclic material.

    Science.gov (United States)

    Hasegawa, Hiroshi; Rahman, Ismail M M; Kinoshita, Sanae; Maki, Teruya; Furusho, Yoshiaki

    2010-03-01

    Although the excellent metal-binding capacities of aminopolycarboxylate chelants (APCs) facilitate their extensive use, pre- and post-toxicity of APCs and their high persistence in aquatic environments evoke concerns. Several treatment techniques with a principal focus on the degradation of APCs at the pre-release step have been proposed. Here, we report a technique for the separation of metal ions from waste solution containing excess APCs using a solid phase extraction system with an ion-selective immobilized macrocyclic material, commonly known as a molecular recognition technology (MRT) gel. Synthetic metal solutions with 100-fold chelant content housed in H2O matrices were used as samples. The MRT gel showed a higher recovery rate compared with other SPE materials at 20 degrees C using a flow rate of 0.2 mL min(-1). The effects of solution pH, metal-chelant stability constants and ionic radii were assessed for 32 metals. Compared to the conventional treatment options for such waste solutions, our proposed technique has the advantage of non-destructive separation of both metal ions and chelants. 2010 Elsevier Ltd. All rights reserved.

  7. Complexation induced phase separation: preparation of composite membranes with a nanometer thin dense skin loaded with metal ions

    KAUST Repository

    Villalobos Vazquez de la Parra, Luis Francisco

    2015-04-21

    We present the development of a facile phase-inversion method for forming asymmetric membranes with a precise high metal ion loading capacity in only the dense layer. The approach combines the use of macromolecule-metal intermolecular complexes to form the dense layer of asymmetric membranes with nonsolvent-induced phase separation to form the porous support. This allows the independent optimization of both the dense layer and porous support while maintaining the simplicity of a phase-inversion process. Moreover, it facilitates control over (i) the thickness of the dense layer throughout several orders of magnitude—from less than 15 nm to more than 6 μm, (ii) the type and amount of metal ions loaded in the dense layer, (iii) the morphology of the membrane surface, and (iv) the porosity and structure of the support. This simple and scalable process provides a new platform for building multifunctional membranes with a high loading of well-dispersed metal ions in the dense layer.

  8. Recycling metals from lithium ion battery by mechanical separation and vacuum metallurgy.

    Science.gov (United States)

    Xiao, Jiefeng; Li, Jia; Xu, Zhengming

    2017-09-15

    The large-batch application of lithium ion batteries leads to the mass production of spent batteries. So the enhancement of disposal ability of spent lithium ion batteries is becoming very urgent. This study proposes an integrated process to handle bulk spent lithium manganese (LiMn 2 O 4 ) batteries to in situ recycle high value-added products without any additives. By mechanical separation, the mixed electrode materials mainly including binder, graphite and LiMn 2 O 4 are firstly obtained from spent batteries. Then, the reaction characteristics for the oxygen-free roasting of mixed electrode materials are analyzed. And the results show that mixed electrode materials can be in situ converted into manganese oxide (MnO) and lithium carbonate (Li 2 CO 3 ) at 1073K for 45min. In this process, the binder is evaporated and decomposed into gaseous products which can be collected to avoid disposal cost. Finally, 91.30% of Li resource as Li 2 CO 3 is leached from roasted powders by water and then high value-added Li 2 CO 3 crystals are further gained by evaporating the filter liquid. The filter residues are burned in air to remove the graphite and the final residues as manganous-manganic oxide (Mn 3 O 4 ) is obtained. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Selective extraction of metal ions from aqueous phase to ionic liquids: a novel thermodynamic approach to separations.

    Science.gov (United States)

    Janssen, Camiel H C; Sánchez, Antonio; Kobrak, Mark N

    2014-11-10

    The selective extraction of metals from aqueous mixtures has generally relied on the use of selective ionophores. We present an alternative strategy that exploits a recently developed approach to extraction into an ionic liquid phase, and show that a high degree of control over selectivity can be obtained by tuning the relative concentrations of extraction agents. A thermodynamic model for the approach is presented, and an experimental separation of strontium and potassium ions is performed. It is shown that tuning the concentrations of the species involved can shift the ratio of potassium to strontium in the ionic liquid phase from 4:1 to 3:4. This extraction is performed under mild conditions with relatively common reagents. The result is a proof-of-concept for a novel separations scheme that could have great importance in a wide range of technological applications. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Preconcentration/separation of some trace metal ions from water samples by a new synthesized chelating resin.

    Science.gov (United States)

    Sener, Seher; Tokalioğlu, Serife; Ozentürk, Ismail; Soykan, Cengiz

    2014-01-01

    A solid phase extractor, poly(N,N'-dipropionitrile methacrylamide-co-divinylbenzene-co-2-acrylamido-2-methyl-1-propanesulfonic acid), was synthesized and used for separation/preconcentration of traces of Ni(II), Co(II), Cu(II), Mn(II), Cd(II), Zn(II), and Pb(II) from various water samples prior to their determination by flame atomic absorption spectrometry. The characterization of the synthesized resin was performed by elemental analysis and IR spectrometry. Parameters such as pH, volume and concentration of the eluent, flow rate of the sample solution, sample volume, and interfering ions affecting the column SPE were examined. The optimum pH was found to be 3. The retained metal ions were desorbed from the column with 10 mL of 1 M HCI eluent. A high preconcentration factor, 40-100; low RSD, method was confirmed by analyzing certified reference materials (TMDA-70 Lake Water and SPS-WW1 Batch 111-Wastewater) and spiked water samples. The method was successfully applied to the determination of metal ions in tap, lake, and dam waters.

  11. Contributions to anionexchange separation of metal ions in mixed aqueous-organic solvent systems

    International Nuclear Information System (INIS)

    Cunha-Campos, C.

    1986-01-01

    In the first chapter of the thesis a method is described for the determination of iron, copper, manganese, nickel, cobalt and uranium in samples of manganese nodules. After dissolution of the sample in a mixture of concentrated hydrochloric-nitric acids, the elements are adsorbed on a column of the strongly basic anion-exchange resin Dowex 1 from a medium consisting of 80% cyclohexanone 10% methanol and 10% 1M hydrochloric acid. Following removal of iron by washing the resin bed with a mixture of the same composition, 90% methanol-10% 1M hydrochloric containing ascorbic acid is passed through the column to eluate manganese, nickel and cobalt. Subsequently, 4M hydrochloric acid-1% hydrogen peroxid solution and 1M hydrochloric acid are used to elute copper and uranium, respectively. The elements were determined quantitatively by ICP-OES, except for uranium which was determined by fluorimetry. The method was used successfully for the determination of mg and p.p.m. quantities of these elements in samples of manganese nodules. In the second chapter of the thesis a procedure is described for the determination of cadmium, lead, zinc and uranium in samples of Austrian mineral waters. After acidification, the sample was heated to expell CO 2 and the elements in the presence of 8-hydroxyquinoline are extracted into chloroform at pH-7. Then the metals are adsorbed on a column of the strongly basic anion-exchange resin Dowex 1 from a medium consisting of 55% chloroform, 36% methanol and 9% 12M hydrochloric acid. After simultaneous elution of the elements with 1M nitric acid, a portion of the eluate was passed through another column containing the same resin to separate uranium from the other elements. The uranium was determined fluorimetrically and cadmium, lead and zinc by atomic absorption spectroscopy. The method was successfully used for the quantitative determination of these elements in mineral water samples. (Author)

  12. Native SDS-PAGE: high resolution electrophoretic separation of proteins with retention of native properties including bound metal ions.

    Science.gov (United States)

    Nowakowski, Andrew B; Wobig, William J; Petering, David H

    2014-05-01

    Sodium dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE) is commonly used to obtain high resolution separation of complex mixtures of proteins. The method initially denatures the proteins that will undergo electrophoresis. Although covalent structural features of resolved proteins can be determined with SDS-PAGE, functional properties are destroyed, including the presence of non-covalently bound metal ions. To address this shortcoming, blue-native (BN)-PAGE has been introduced. This method retains functional properties but at the cost of protein resolving power. To address the need for a high resolution PAGE method that results in the separation of native proteins, experiments tested the impact of changing the conditions of SDS-PAGE on the quality of protein separation and retention of functional properties. Removal of SDS and EDTA from the sample buffer together with omission of a heating step had no effect on the results of PAGE. Reduction of SDS in the running buffer from 0.1% to 0.0375% together with deletion of EDTA also made little impact on the quality of the electrophoretograms of fractions of pig kidney (LLC-PK1) cell proteome in comparison with that achieved with the SDS-PAGE method. The modified conditions were called native (N)SDS-PAGE. Retention of Zn(2+) bound in proteomic samples increased from 26 to 98% upon shifting from standard to modified conditions. Moreover, seven of nine model enzymes, including four Zn(2+) proteins that were subjected to NSDS-PAGE retained activity. All nine were active in BN-PAGE, whereas all underwent denaturation during SDS-PAGE. Metal retention after electrophoresis was additionally confirmed using laser ablation-inductively coupled plasma-mass spectrometry and in-gel Zn-protein staining using the fluorophore TSQ.

  13. Immobilized chiral tropine ionic liquid on silica gel as adsorbent for separation of metal ions and racemic amino acids.

    Science.gov (United States)

    Qian, Guofei; Song, Hang; Yao, Shun

    2016-01-15

    Tropine-type chiral ionic liquid with proline anion was immobilized on silica gel by chemical modification method for the first time, which was proved by elemental, infrared spectrum and thermogravimetric analysis. Secondly, the performance of this kind of ionic liquid-modified silica gel was investigated in the adsorption of some metal ions, which included Cu(2+), Fe(3+), Mn(2+) and Ni(2+). Then the effects of time, initial concentration and temperature on adsorption for Cu(2+) ions were studied in detail, which was followed by the further research of adsorption kinetics and thermodynamics. The adsorption could be better described by pseudo-second-order kinetics model and that the process was spontaneous, exothermic and entropy decreasing. In the mode of 'reuse after adsorption', the ionic liquid-modified silica gel with saturated adsorption of Cu(2+) was finally used in resolution of racemic amino acids for the first time. The static experiment showed that adsorption rate of two enantiomers was obviously different. Inspired by this, the complex was packed in chromatographic column for the separation of racemic amino acids and d-enantiomers were firstly eluted by water or ethanol. Steric hindrance was found as one of key influencing factors for its effect on the stability of the complex. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. Separation of metal ions by anion exchange in mixtures of hydrochloric acid and hydrofluoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Faris, J.P.

    1978-12-01

    Distribution coefficients were determined for the adsorption of more than 40 elements on anion-exchange resins from mixtures of HCl (0.1 to 12M) and HF (0.1-8M). Two resins, Dowex 1 x 10, 200 to 400 mesh and Dowex 1 x 4, 100 to 200 mesh, were used. Distribution coefficients were also determined for the adsorption of many elements on both resins from 0.1 to 12M HCl and 0.1 to 12M HF. Anion exchange in the presence of HF was found useful for separating impurities from various materials for their subsequent determination, and specific procedures used in our spectrochemical laboratory for this purpose are outlined. The results of a literature search on the use of anion exchange in hydrofluoric acid and fluoride-containing media are presented in an extensive bibliography. 404 references, 9 tables.

  15. Separation of metal ions by anion exchange in mixtures of hydrochloric acid and hydrofluoric acid

    International Nuclear Information System (INIS)

    Faris, J.P.

    1978-12-01

    Distribution coefficients were determined for the adsorption of more than 40 elements on anion-exchange resins from mixtures of HCl (0.1 to 12M) and HF (0.1-8M). Two resins, Dowex 1 x 10, 200 to 400 mesh and Dowex 1 x 4, 100 to 200 mesh, were used. Distribution coefficients were also determined for the adsorption of many elements on both resins from 0.1 to 12M HCl and 0.1 to 12M HF. Anion exchange in the presence of HF was found useful for separating impurities from various materials for their subsequent determination, and specific procedures used in our spectrochemical laboratory for this purpose are outlined. The results of a literature search on the use of anion exchange in hydrofluoric acid and fluoride-containing media are presented in an extensive bibliography. 404 references, 9 tables

  16. Synthesis and Ion-Exchange Properties of Graphene Th(IV) Phosphate Composite Cation Exchanger: Its Applications in the Selective Separation of Lead Metal Ions

    OpenAIRE

    Rangreez, Tauseef Ahmad; Inamuddin,; Asiri, Abdullah M.; Alhogbi, Basma G.; Naushad, Mu.

    2017-01-01

    In this study, graphene Th(IV) phosphate was prepared by sol?gel precipitation method. The ion-exchange behavior of this cation-exchanger was studied by investigating properties like ion-exchange capacity for various metal ions, the effect of eluent concentration, elution behavior, and thermal effect on ion-exchange capacity (IEC). Several physicochemical properties as Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) study, thermal studies, scanning electron microscopy ...

  17. Selective Single-Step Separation of a Mixture of Three Metal Ions by a Triphasic Ionic-Liquid-Water-Ionic-Liquid Solvent Extraction System.

    Science.gov (United States)

    Vander Hoogerstraete, Tom; Blockx, Jonas; De Coster, Hendrik; Binnemans, Koen

    2015-08-10

    In a conventional solvent extraction system, metal ions are distributed between two immiscible phases, typically an aqueous and an organic phase. In this paper, the proof-of-principle is given for the distribution of metal ions between three immiscible phases, two ionic liquid phases with an aqueous phase in between them. Three-liquid-phase solvent extraction allows separation of a mixture of three metal ions in a single step, whereas at least two steps are required to separate three metals in the case of two-liquid-phase solvent extraction. In the triphasic system, the lower organic phase is comprised of the ionic liquid betainium- or choline bis(trifluoromethylsulfonyl)imide, whereas the upper organic phase is comprised of the ionic liquid trihexyl(tetradecyl)phosphonium bis(trifluoromethylsulfonyl)imide. The triphasic system was used for the separation of a mixture of tin(II), yttrium(III), and scandium(III) ions. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Toxic metal ion separation by cellulose acetate/sulfonated poly(ether imide) blend membranes: effect of polymer composition and additive.

    Science.gov (United States)

    Nagendran, A; Vijayalakshmi, A; Arockiasamy, D Lawrence; Shobana, K H; Mohan, D

    2008-07-15

    Toxic heavy metal ion removal from industrial effluents are gaining increased visibility owing to environmental concern and saving precious materials. In this work, an attempt has been made to remove the valuable metal ions using modified ultrafiltration (UF) blend membranes based on cellulose acetate (CA) and sulfonated poly(ether imide) (SPEI) were prepared in the presence and absence of additive, poly(ethylene glycol) 600 (PEG600) in various compositions. Prepared membranes were characterized in terms of pure water flux (PWF), water content and membrane hydraulic resistance. High flux UF membranes were obtained in the range of 15-25 wt% SPEI and 2.5-10 wt% PEG600 in the polymer blend. The molecular weight cut-off (MWCO) of the blend membranes were determined using protein separation studies found to vary from 20 to greater than 69 kDa. Surface morphology of the blend membranes were analysed with scanning electron microscopy. Studies were carried out to find the rejection and permeate flux of metal ions such as Cu(II), Ni(II), Zn(II) and Cd(II) using polyethyleneimine as the chelating ligand. On increasing the composition of SPEI and PEG600, the rejection of metal ions is decreasing while the permeate flux has an increasing trend. These effects are due to the increased pore formation in the CA/SPEI blend membranes because of the hydrophilic SPEI and polymeric additive PEG600. In general, it was found that CA/SPEI blend membranes displayed higher permeate flux and lower rejection compared to pure CA membranes. The extent of separation of metal ions depends on the affinity of metal ions to polyethyleneimine to form macromolecular complexes and the stability of the formed complexes.

  19. Ion implantation in metals

    International Nuclear Information System (INIS)

    Vook, F.L.

    1977-02-01

    The application of ion beams to metals is rapidly emerging as a promising area of research and technology. This report briefly describes some of the recent advances in the modification and study of the basic properties of metals by ion implantation techniques. Most of the research discussed illustrates some of the new and exciting applications of ion beams to metals which are under active investigation at Sandia Laboratories, Albuquerque

  20. Attainable gravimetric and volumetric energy density of Li-S and li ion battery cells with solid separator-protected Li metal anodes.

    Science.gov (United States)

    McCloskey, Bryan D

    2015-11-19

    As a result of sulfur's high electrochemical capacity (1675 mA h/gs), lithium-sulfur batteries have received significant attention as a potential high-specific-energy alternative to current state-of-the-art rechargeable Li ion batteries. For Li-S batteries to compete with commercially available Li ion batteries, high-capacity anodes, such as those that use Li metal, will need to be enabled to fully exploit sulfur's high capacity. The development of Li metal anodes has focused on eliminating Coulombically inefficient and dendritic Li cycling, and to this end, an interesting direction of research is to protect Li metal by employing mechanically stiff solid-state Li(+) conductors, such as garnet phase Li7La3Zr2O12 (LLZO), NASICON-type Li1+xAlxTi2-x(PO4)3 (LATP), and Li2S-P2S5 glasses (LPS), as electrode separators. Basic calculations are used to quantify useful targets for solid Li metal protective separator thickness and cost to enable Li metal batteries in general and Li-S batteries specifically. Furthermore, maximum electrolyte-to-sulfur ratios that allow Li-S batteries to compete with Li ion batteries are calculated. The results presented here suggest that controlling the complex polysulfide speciation chemistry in Li-S cells with realistic, minimal electrolyte loading presents a meaningful opportunity to develop Li-S batteries that are competitive on a specific energy basis with current state-of-the-art Li ion batteries.

  1. SEPARATION OF Fe (III, Cr(III, Cu(II, Ni(II, Co(II, AND Pb(II METAL IONS USING POLY(EUGENYL OXYACETIC ACID AS AN ION CARRIER BY A LIQUID MEMBRANE TRANSPORT METHOD

    Directory of Open Access Journals (Sweden)

    La Harimu

    2010-06-01

    Full Text Available Fe (III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II  metal ions had been separated using poly(eugenyl oxyacetic acid as an ion carrier by bulk liquid membrane transport method. The effect of pH, polyeugenyl oxyacetic acid ion carrier concentration, nitric acid concentration in the stripping solution, transport time, and metal concentration were optimized. The result showed that the optimum condition for transport of metal ions was at pH 4 for ion Fe(III and at pH 5 for Cr(III, Cu(II, Ni(II, Co(II, and Pb(II ions. The carrier volumes were optimum with concentration of 1 x 10-3 M at 7.5 mL for Cr(III, Cu (II,  Ni(II, Co(II ions and at 8.5 mL for Fe(III and Pb(II ions. The concentration of HNO3 in stripping phase was optimum at 2 M for Fe(III and Cu(II ions, 1 M for Cr(III, Ni(II and Co(II ions, and 0.5 M for Pb(II ion. The optimum transport times were 36 h for Fe(III and Co(II ions, and 48 h for Cr(III, Cu (II, Ni(II, and Pb(II ions. The concentration of metal ions accurately transported were 2.5 x 10-4 M for Fe(III and Cr(III ions, and 1 M for Cu (II, Ni(II, Co(II, and Pb(II ions. Compared to other metal ions the transport of Fe(III was the highest with selectivity order of Fe(III > Cr(III > Pb(II > Cu(II > Ni(II > Co(II. At optimum condition, Fe(III ion was transported through the membrane at 46.46%.   Keywords: poly(eugenyl oxyacetic acid, transport, liquid membrane, Fe (III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II ions

  2. Development of methods for immobilisation of crown ethers onto solid supports for separation of metal ions from solution

    International Nuclear Information System (INIS)

    Wagh, Sandip Janardan; Renjithkumar, A.U.; Maithania, K.N.; Mukhopadhyay, Sulekha; Shenoy, K.T.; Ghosh, Sunil Kumar

    2014-01-01

    Since the serendipitous discovery of dibenzo-18-crown-6 (1) by C.J. Pedersen in 1967, many significant developments have been made in the field of host-guest chemistry. The very important use of these molecules in nuclear industry is removal of metal ions selectively. The removal of 90 Sr from the nuclear waste solution is very essential in order to reduce the vitrification period. Dicyclohexyl 18 Crown 6 ether (hydrogenated form of 1) has been reported to be efficient selective ligand for recovery of 90 Sr from nitrate medium. The application of crown ether in liquid-liquid extraction mode has some issue related to choice of diluents and aqueous solubility. Both of these problems can be overcome by the incorporation of crown ethers onto polymers. Polymer supported reagents offer many advantages, including ease of handling and recoverability when used in the removal of toxic metal ions from the environment. Due to increased concern with the remediation of wastewater, polymer-supported reagents, including immobilized crown ethers, have been studied for the selective removal of targeted metal ions. This will allow ease of handling, recyclability and adaption to continuous processes. There are three principal methods by which crown ethers can be incorporated into polymer matrices a) step-growth mechanism; b) chain-growth mechanism; c) post-functionalization wherein a crown ether is covalently bound to a pre-formed polymer backbone. The last method requires the crown to have a reactive functional group that can bond to the polymer. The immobilisation of (1) and (2) onto a solid support zeocarb-226 via amide linkage is successfully achieved by our group. We have synthesized novel extraction chromatographic resins by covalently binding on polymeric substrate. The covalent bonding in synthesized polymeric material has characterized by the FTIR. The resultant material is providing a simple and effective means of isolating 90 Sr and 6 Li

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

    Science.gov (United States)

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

    1999-05-25

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

  4. Metal Ions Analysis with Capillary Zone Electrophoresis.

    Science.gov (United States)

    Malik, Ashok Kumar; Aulakh, Jatinder Singh; Kaur, Varinder

    2016-01-01

    Capillary electrophoresis has recently attracted considerable attention as a promising analytical technique for metal ion separations. Significant advances that open new application areas for capillary electrophoresis in the analysis of metal species occurred based on various auxiliary separation principles. These are mainly due to complexation, ion pairing, solvation, and micellization interactions between metal analytes and electrolyte additives, which alter the separation selectivity in a broad range. Likewise, many separation studies for metal ions have been concentrated on the use of preelectrophoresis derivatization methodology. Approaches suitable for manipulation of selectivity for different metal species including metal cations, metal complexes, metal oxoanions, and organometallic compounds, are discussed, with special attention paid to the related electrophoretic system variables using illustrative examples.

  5. Polystyrene Sulfonate Threaded through a Metal-Organic Framework Membrane for Fast and Selective Lithium-Ion Separation.

    Science.gov (United States)

    Guo, Yi; Ying, Yulong; Mao, Yiyin; Peng, Xinsheng; Chen, Banglin

    2016-11-21

    Extraction of lithium ions from salt-lake brines is very important to produce lithium compounds. Herein, we report a new approach to construct polystyrene sulfonate (PSS) threaded HKUST-1 metal-organic framework (MOF) membranes through an in situ confinement conversion process. The resulting membrane PSS@HKUST-1-6.7, with unique anchored three-dimensional sulfonate networks, shows a very high Li + conductivity of 5.53×10 -4  S cm -1 at 25 °C, 1.89×10 -3  S cm -1 at 70 °C, and Li + flux of 6.75 mol m -2  h -1 , which are five orders higher than that of the pristine HKUST-1 membrane. Attributed to the different size sieving effects and the affinity differences of the Li + , Na + , K + , and Mg 2+ ions to the sulfonate groups, the PSS@HKUST-1-6.7 membrane exhibits ideal selectivities of 78, 99, and 10296 for Li + /Na + , Li + /K + , Li + /Mg 2+ and real binary ion selectivities of 35, 67, and 1815, respectively, the highest ever reported among ionic conductors and Li + extraction membranes. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Development of a flotation method for preconcentration-separation of trace amounts of some metal ions in plant tissues prior to their FAAS determinations

    Directory of Open Access Journals (Sweden)

    M. Ghaedi

    2010-01-01

    Full Text Available An efficient flotation method based on the combination of flame atomic absorption spectrometry (FAAS and separation and preconcentration step for determination of Cr3+, Cu 2+, Co2+, Ni2+, Zn2+, Cd 2+, Fe3+ and Pb2+ ions in various real samples by the possibility of applying bis(2-hydroxyacetophenone-1,4-butanediimine (BHABDI as a new collector was studied. The influence of pH, amount of BHABDI as collector, sample matrix, type and amount of eluting agent, type and amount of surfactant as floating agent, ionic strength and air flow rates i.e. variables affecting the efficiency of the extraction system was evaluated. It is ascertained that metal ions such as iron can be separated simultaneously from matrix in the presence of 0.012 mM ligand, 0.025% (w/v of CTAB to a test sample of 750 mL at pH 6.5. These ions can be eluted quantitatively with 6 mL of 1.0 mol L-1 HNO3 in methanol which lead to the enrichment factor of 125. The detection limits for analyte ions were in the range of 1.3-2.4 ng mL-1. The method has been successfully applied for determination of trace amounts of ions in various real samples.

  7. Separators for Li-Ion and Li-Metal Battery Including Ionic Liquid Based Electrolytes Based on the TFSI− and FSI− Anions

    Directory of Open Access Journals (Sweden)

    Marija Kirchhöfer

    2014-08-01

    Full Text Available The characterization of separators for Li-ion or Li-metal batteries incorporating hydrophobic ionic liquid electrolytes is reported herein. Ionic liquids made of N-butyl-N-methylpyrrolidinium (PYR14+ or N-methoxyethyl-N-methylpyrrolidinium (PYR12O1+, paired with bis(trifluoromethanesulfonylimide (TFSI− or bis(fluorosulfonylimide (FSI− anions, were tested in combination with separators having different chemistries and morphologies in terms of wetting behavior, Gurley and McMullin number, as well as Li/(Separator + Electrolyte interfacial properties. It is shown that non-functionalized microporous polyolefin separators are poorly wetted by FSI−-based electrolytes (contrary to TFSI−-based electrolytes, while the ceramic coated separator Separion® allows good wetting with all electrolytes. Furthermore, by comparing the lithium solid electrolyte interphase (SEI resistance evolution at open circuit and during cycling, depending on separator morphologies and chemistries, it is possible to propose a scale for SEI forming properties in the order: PYR12O1FSI > PYR14FSI > PYR14TFSI > PYR12O1TFSI. Finally, the impact the separator morphology is evidenced by the SEI resistance evolution and by comparing Li electrodes cycled using separators with two different morphologies.

  8. Isotopic separation by ion chromatography

    International Nuclear Information System (INIS)

    Albert, M.G.; Barre, Y.; Neige, R.

    1994-01-01

    The isotopic exchange reaction and the isotopic separation factor are first recalled; the principles of ion chromatography applied to lithium isotope separation are then reviewed (displacement chromatography) and the process is modelled in the view of dimensioning and optimizing the industrial process; the various dimensioning parameters are the isotopic separation factor, the isotopic exchange kinetics and the material flow rate. Effects of the resin type and structure are presented. Dimensioning is also affected by physico-chemical and hydraulic parameters. Industrial implementation features are also discussed. 1 fig., 1 tab., 5 refs

  9. Metals Separation by Liquid Extraction.

    Science.gov (United States)

    Malmary, G.; And Others

    1984-01-01

    As part of a project focusing on techniques in industrial chemistry, students carry out experiments on separating copper from cobalt in chloride-containing aqueous solution by liquid extraction with triisoctylamine solvent and search the literature on the separation process of these metals. These experiments and the literature research are…

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

    Science.gov (United States)

    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"…

  11. SYNTHESIS OF POLYEUGENYL OXYACETIC ACID AS A CARRIER TO SEPARATE HEAVY METAL ION Fe (III, Cr(III, Cu(II, Ni(II, Co(II, AND Pb(II THAT USING SOLVENT EXTRACTION METHOD

    Directory of Open Access Journals (Sweden)

    La Harimu

    2010-06-01

    Full Text Available Polyeugenyl oxyacetic acid has been synthesized from polyeugenol and chloroacetic acid and applied to separate metal Fe(III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II using solvent extraction method. pH effect, polyeugenyl oxyacetic acid ion carrier concentration, extraction time, and metal concentration optimized to gain optimum condition. The result of experiment indicated that polyeugenyl oxyacetic acid resulted the yellowed brown synthesis with melting point 125 °C and yield 68.9%. The Characterization of spectroscopy IR attributed by absorption to the area 1735,8 cm -1 as carbonyl extend vibration (C=O acid and 1H-NMR that was attributed by chemical shift at 4.6 ppm as carboxy proton (CH2-C=0. The metal separation optimum condition gained pH 3-6 for ion Fe(III, pH 5 for ion Cr(III, Ni(II, and Co(II and pH 6 for ion Cu(II, and Pb(II. Optimum carrier concentraction 5 mL, 10 mL, and 15 mL for ion Fe(III, and ion Cr(III, Ni(II, Co(II, and ion Cu(II, Pb(II respectively. Extraction time 2.5 h for ion Fe(III, 20 h for ion Cr(III, and 36 h for ion Cu(II, Pb(II, Ni(II, and Co(II. Metal concentration that would extracted correctly (0.75-5 x 10-4 M for ion Fe(III, (0.75-2.5 x 10-4 M for ion Cr(III, Ni(II, and Co(II and (0.75-1 x 10-4 M for ion Cu(II and Pb(II. The best polyeugenil oxyacetic acid response to separate ion Fe(III than other ions with selectivity order Fe(III> Cr(III> Cu(II> Pb(II> Ni(II> Co(II.   Keywords: polyeugenil oxyacetic acid, pH, extraction time, metal concentraction, solvent extraction

  12. Ion mass separation modeling inside a plasma separator

    Science.gov (United States)

    Gavrikov, A. V.; Sidorov, V. S.; Smirnov, V. P.; Tarakanov, V. P.

    2018-01-01

    The results have been obtained in a continuation of the work for ion trajectories calculation in crossed electric and magnetic fields and also in a close alignment with the plasma separation study development. The main task was to calculate trajectories of ions of the substance imitating spent nuclear fuel in order to find a feasible plasma separator configuration. The three-dimensional modeling has been made with KARAT code in a single-particle approximation. The calculations have been performed under the following conditions. Magnetic field is produced by 2 coils of wire, the characteristic field strength in a uniform area is 1.4 kG. Electric field is produced by several electrodes (axial ones, anode shell and capacitor sheets) with electric potential up to 500 V. The characteristic linear size of the cylindrical separator area is ∼ 100 cm. The characteristic size of injection region is ∼ 1 cm. Spatial position of the injection region is inside the separator. The injection direction is along magnetic lines. Injected particles are single-charged ions with energies from 0 to 20 eV with atomic masses A = 150 and 240. Wide spreading angle range was investigated. As a result of simulation a feasible separator configuration was found. This configuration allows to achieve more than 10 cm spatial division distance for the separated ions and is fully compliant with and supplementary to the vacuum arc-based ion source research.

  13. Simultaneous enrichment-separation of metal ions from environmental samples by solid-phase extraction using double-walled carbon nanotubes.

    Science.gov (United States)

    Soylak, Mustafa; Unsal, Yunus Emre

    2009-01-01

    A solid-phase extraction (SPE) method has been developed using a column filled with double-walled carbon nanotubes for the preconcentration-separation of Co(II), Cu(II), Ni(II), Pb(II), Fe(III), and Mn(ll) ions. Experimental parameters, including pH of the solution, sample volume, flow rate of the sample solution and eluents, etc., were investigated. Quantitative recoveries for the anayte ions were obtained at pH 9.0 with 2 M HNO3 eluent at a flow rate of 2 mL/min. The influences of matrix ions were also investigated. The preconcentration factor was 100. Addition and recovery experiments for analyte ions in real water samples gave good results. The validity of the presented SPE method was tested by analysis of HR-1 Humber River Sediment certified reference material for each element.

  14. Application of PVDF composite for lithium-ion battery separator

    International Nuclear Information System (INIS)

    Sabrina, Q.; Majid, N.; Prihandoko, B.

    2016-01-01

    In this study a composite observed in PVDF composite as lithium ion battery separator. Observation of performance cell battery with cyclic voltametry and charge discharge capacity. Surface morphology PVDF separator and commercial separator observed with Scanning electron microscopy (SEM). Cyclic Voltamerty test (CV) and Charge Discharge (CD) showed a capacity value on the coin cell. Coin cell is composed of material LiFePO 4 cathode, anode material of lithium metal and varies as graphite, liquid electrolyte varied use LiBOB and LiPF 6 . While the PVDF as compared to the commercial separator. Coin cell commercial separator has a better high capacity value when compared with Coin cell with the PVDF separator. Life cycle coin cell with the commercial separator material is still longer than coin cell separator with PVDF Copolymer. Development of PVDF as separator remains to be done in order to improve the performance of the battery exceeds the usage of commercial material. (paper)

  15. Metal vapor vacuum arc ion sources

    International Nuclear Information System (INIS)

    Brown, I.G.; Dickinson, M.R.; Galvin, J.E.; Godechot, X.; MacGill, R.A.

    1990-06-01

    We have developed a family of metal vapor vacuum are (MEVVA) high current metal ion sources. The sources were initially developed for the production of high current beams of metal ions for heavy ion synchrotron injection for basic nuclear physics research; more recently they have also been used for metal ion implantation. A number of different embodiments of the source have been developed for these specific applications. Presently the sources operate in a pulsed mode, with pulse width of order 1 ms and repetition rate up to 100 pps. Beam extraction voltage is up to 100 kV, and since the ions produced in the vacuum arc plasma are in general multiply ionized the ion energy is up to several hundred keV. Beam current is up to several Amperes peak and around 10 mA time averaged delivered onto target. Nearly all of the solid metals of the Periodic Table have been use to produce beam. A number of novel features have been incorporated into the sources, including multiple cathodes and the ability to switch between up to 18 separate cathode materials simply and quickly, and a broad beam source version as well as miniature versions. here we review the source designs and their performance. 45 refs., 7 figs

  16. Sorption of metal ions on synthetic organo-inorganic ion exchanger polyacrylonitrile-Ti(IV) tungstophosphate

    International Nuclear Information System (INIS)

    Haidary, A.; Ahmadi, S. J.; Asadi, M. R.; Asgharizadeh, F.; Ashtari, P.

    2010-01-01

    In this study two Polyacrylonitrile-Ti(IV) tungstophosphate organo-inorganic ion exchangers with different molar ratios have been synthesized. These ion exchangers have been characterized by fourier transform-IR, X- ray diffraction, thermal gravimetric, scanning electron microscopy and CHNSO techniques and their cation exchange capacity bas been measured by continuous method. Distribution coefficients (K d ) for metal ions and radionuclides were determined by batch method and with these ion exchangers, separation of metal ions was achieved on a glass column.

  17. Adsorption of peptides and small proteins with control access polymer permeation to affinity binding sites. Part I: Polymer permeation-immobilized metal ion affinity chromatography separation adsorbents with polyethylene glycol and immobilized metal ions.

    Science.gov (United States)

    González-Ortega, Omar; Porath, Jerker; Guzmán, Roberto

    2012-03-02

    Despite the many efforts to develop efficient protein purification techniques, the isolation of peptides and small proteins on a larger than analytical scale remains a significant challenge. Recovery of small biomolecules from diluted complex biological mixtures, such as human serum, employing porous adsorbents is a difficult task mainly due to the presence of concentrated large biomolecules that can add undesired effects in the system such as blocking of adsorbent pores, impairing diffusion of small molecules, or competition for adsorption sites. Adsorption and size exclusion chromatography (AdSEC) controlled access media, using polyethylene glycol (PEG) as a semi-permeable barrier on a polysaccharide matrix, have been developed and explored in this work to overcome such effects and to preferentially adsorb small molecules while rejecting large ones. In the first part of this work, adsorption studies were performed with small peptides and proteins from synthetic mixtures using controlled access polymer permeation adsorption (CAPPA) media created by effectively grafting PEG on an immobilized metal affinity chromatography (IMAC) agarose resin, where chelating agents and immobilized metal ions were used as the primary affinity binding sites. Synthetic mixtures consisted of bovine serum albumin (BSA) with small proteins, peptides, amino acids (such as histidine or Val⁴-Angiotensin III), and small molecules-spiked human serum. The synthesized hybrid adsorbent consisted of agarose beads modified with iminodiacetic (IDA) groups, loaded with immobilized Cu(II) ions, and PEG. These CAPPA media with grafted PEG on the interior and exterior surfaces of the agarose matrix were effective in rejecting high molecular weight proteins. Different PEG grafting densities and PEG of different molecular weight were tested to determine their effect in rejecting and controlling adsorbent permeation properties. Low grafting density of high molecular weight PEG was found to be as

  18. Combination of flotation and flame atomic absorption spectrometry for determination, preconcentration and separation of trace amounts of metal ions in biological samples.

    Science.gov (United States)

    Ghaedi, Mehrorang; Niknam, Khodabakhsh; Nasiri kokhdan, Syamak; Soylak, Mustafa

    2013-05-01

    An efficient enrichment procedure based on the combination of flame atomic absorption spectrometry (FAAS) and flotation for determination of Cd(2+), Ag(+) and Zn(2+) ions in various biological samples using new collector is studied. The influence of pH, amount of 2-(((1H-benzo[d]imidazol-2-yl)methoxy)methyl)-1H-benzo[d]imidazole (HBIMMHBI) as collector, sample matrix, type and amount of eluting agent, type and amount of surfactant as floating agent, ionic strength and air flow rates on the extraction efficiency were evaluated and optimized. It is ascertained that under study metal ions is preconcentrated simultaneously from matrix in the presence of 0.005 M HBIMMHBI, 0.085% (w/v) of SDS form 750 mL at pH 6.5. The floated complexes metal ions eluted quantitatively with 6 mL of 1.0 M HNO3 in methanol lead to achieve preconcentration factor of 125. The detection limits for analyte ions were in the range of 1.3-2.4 ng mL(-1), with recoveries more than 95% and relative SD lower than 4%.

  19. Pure inorganic separator for lithium ion batteries.

    Science.gov (United States)

    He, Meinan; Zhang, Xinjie; Jiang, Kuiyang; Wang, Joe; Wang, Yan

    2015-01-14

    Battery safety is critical for many applications including portable electronics, hybrid and electric vehicles, and grid storage. For lithium ion batteries, the conventional polymer based separator is unstable at 120 °C and above. In this research, we have developed a pure aluminum oxide nanowire based separator; this separator does not contain any polymer additives or binders; additionally, it is a bendable ceramic. The physical and electrochemical properties of the separator are investigated. The separator has a pore size of about 100 nm, and it shows excellent electrochemical properties under both room and high temperatures. At room temperature, the ceramic separator shows a higher rate capability compared to the conventional Celgard 2500 separator and life cycle performance does not show any degradation. At 120 °C, the cell with the ceramic separator showed a much better cycle performance than the conventional Celgard 2500 separator. Therefore, we believe that this research is really an exciting scientific breakthrough for ceramic separators and lithium ion batteries and could be potentially used in the next generation lithium ion batteries requiring high safety and reliability.

  20. EFFICIENCY OF METAL SCRAP SEPARATION IN EDDY CURRENT SEPARATOR

    Directory of Open Access Journals (Sweden)

    Gordan Bedeković

    2008-11-01

    Full Text Available Eddy-current separation is most often method used for the recovery of non-ferrous metals (Al, Cu, Zn, Pb from solid wastes and also for separating non-ferrous metals from each other. The feed material comes to rotary drum and magnetic field by belt conveyer. The changing magnetic field induce eddy currents in conductive (metallic particles. Because interaction between this currents and the magnetic field electrodynamic forces will act on conductive particles. Therefore the trajectories of conductive particles will be different from the trajectories of the non-conductive ones. Separation is a result of the combined actions of several forces (electrodynamic, gravitational and frictional. The paper presents results of aluminium recovery from mixture of metallic particles in eddy current separator. Testing were conducted under field condition. Results shows that is possible achieve recovery of 99 % and concentrate quality of 89 % of aluminium (the paper is published in Croatian.

  1. Method and device for ion mobility separations

    Science.gov (United States)

    Ibrahim, Yehia M.; Garimella, Sandilya V. B.; Smith, Richard D.

    2017-07-11

    Methods and devices for ion separations or manipulations in gas phase are disclosed. The device includes a single non-planar surface. Arrays of electrodes are coupled to the surface. A combination of RF and DC voltages are applied to the arrays of electrodes to create confining and driving fields that move ions through the device. The DC voltages are static DC voltages or time-dependent DC potentials or waveforms.

  2. An equilibrium model for ligand-modified micellar-enhanced ultrafiltration. Selective separation of metal ions using iminoacetic substituted polyamines and a theoretical model for the titration behavior of polyamines

    Energy Technology Data Exchange (ETDEWEB)

    Dharmawardana, Udeni Rajaratna [Univ. of Oklahoma, Norman, OK (United States)

    1992-01-01

    This thesis consists of three chapters. Chapter 1, An equilibrium model for ligand-modified micellar-enhanced ultrafiltration, describes a theoretical model and experimental investigations which used the semi-equilibrium-dialysis method with N-n-dodecyl iminodiacetic acid as the ligand. In Chapter 2, Selective separation of metal ions using iminoacetic substituted polyamines, polyamines with a substituted ligand group are synthesized and used in investigating selective separation of copper ions from aqueous solution. In Chapter 3, A theoretical model for the titration behavior of polyamines, a novel approach to explain the titration behavior of polymeric amines based on the binding behavior of counterions is described. The application of this study is to the investigation of inexpensive and efficient methods of industrial waste water treatment.

  3. Separation of cesium by ion exchange columns

    International Nuclear Information System (INIS)

    Bonini, Alberto; Falcon, Marcelo F.; Devida, Claudio A.; Tadey, D.; Vaccaro, Jorge O.; Maset, Elvira

    2003-01-01

    Crystalline silico titanate (CST) has been tested as a selective inorganic ion exchanger to separate Cs 137 from the residual fission product s solution of the Mo 99 plant. The tests are described in detail and show decontamination factors higher than 6000 and a good elution yield

  4. Rapid ion-exchange separations of actinides

    International Nuclear Information System (INIS)

    Usuda, Shigekazu

    1988-01-01

    For the purpose of studying short-lived actinide nuclides, three methods for rapid ion exchange separation of actinide elements with mineral acid-alcohol mixed media were developed: anion exchange with nitric acid-methyl alcohol mixed media to separate the transplutonium and rare earth elements from target material, U or Pu and Al catcher foils; anion exchange with hydrochloric acid-methyl alcohol media to separate Am+Cm, Bk and Cf+Fm from the target, catcher foils and major fission products; and cation exchange with hydrochloric acid-methyl alcohol media and with concentrated hydrochloric acid to separate the transplutonium elements as a group from the rare earths after eliminating the large amounts of U, Al, Cu, Fe etc. The methods enable one to perform rapid and effective separation at elevated temperature (90 deg C) and immediate source preparation for alpha-ray spectrometry. (author) 47 refs.; 10 figs

  5. Metal separation from multi metallic solutions by grape stalks

    OpenAIRE

    Stevens, Bas

    2016-01-01

    With the rapid development of various industries such as mine and metallurgy, wastewaters containing metals are directly or indirectly discharged into the environment. One of the most dangerous effluents discharged are Acid Mine Drainage (AMD), the outflows of acidic waters from metal mines. This water needs to be treated so it can be reused and the metal ions in this polluted water can be recuperated. The metals that occur in the polluted water are difficult to eliminate. To e...

  6. Studies on the Use of Gamma Radiation-Induced for Preparation of Some Modified Resins for the Separation of Some Metal Ions

    International Nuclear Information System (INIS)

    Abo-Zahra, S.F.

    2012-01-01

    The work carried out in the present thesis is based on preparation, characterization and applications of some modified resins such as: poly(acrylamide)/poly(maleic acid) P(AAm)/P(MA) interpolymer complex (resin), poly(acrylamide-acrylic acid-amidoxime) P(AAm-AA-AO) resin and poly(hydroxamic acid) P(HA) resin. Poly(acrylamide)/poly(maleic acid) P(AAm)/P(MA) interpolymer complex (resin) was prepared by template polymerization of maleic acid (MA) monomer on poly(acrylamide) P(AAm) hydrogel as a template polymer in the presence of N,N'-methylenebisacrylamide (NMBA) as a crosslinker using gamma radiation-induced technique. Poly(acrylamide-acrylic acid-amidoxime) P(AAm-AA-AO) resin was prepared by template polymerization of acrylic acid (AA) and acrylonitrile (AN) monomers on P(AAm) hydrogel as a template polymer in the presence of NMBA as a crosslinker using gamma radiation-induced technique. The conversion of nitrile group to amidoxime one was carried out by the treatment of the prepared resin with an alkaline solution of hydroxylamine. Poly(hydroxamic acid) P(HA) resin was prepared from the reaction of the corresponding water-soluble P(AAm) previously prepared by gamma radiation-induced with hydroxylamine hydrochloride in an alkaline medium. The functional groups on the prepared polymeric resins were confirmed by using Fourier transform infrared (FTIR) spectra. Thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) measurements, scanning electron microscopy (SEM) and electron spin resonance (ESR) measurements were performed to evaluate the properties of the prepared polymeric resins, free or complexed with metal ions such as Cu 2+ metal ions.

  7. Experiments with SIRA - the radioactive ion separator

    International Nuclear Information System (INIS)

    Angelique, J.C.; Orr, N.A.

    1998-01-01

    There are two main techniques to obtain radioactive ion beams. One, consisting in the fragmentation of projectile in a thin target followed by a separation carried out with LISE or SISSI type spectrometers or by an alpha spectrometer is used currently at GANIL. The second one, the ISOL (Isotope Separator One-Line) is presently under study on the SIRa benchmark, as part of the SPIRaL (Source de Production d'Ions Radioactifs en Ligne). A high energy light ion beam is stopped by a thick target to produce radioactive nuclei by various reactions in the target. The target, usually of carbon, is heated at around 1800 deg. C in order to accelerate the migration of the atoms produced at the target surface. These atoms are then diffused by a transfer tube up to plasma region where they are ionized and then accelerated. As projectiles the GANIL project makes use of a large variety of heavy ions. A table containing the radioactive ion beam characteristics (charge state and lifetime), the primary beams, the yields and the expected intensities to be obtained with SPIRaL is presented. Also, data concerning the production rates of rare gases obtained during 1993 to 1994 are given

  8. Separations of actinides, lanthanides and other metals

    Science.gov (United States)

    Smith, Barbara F.; Jarvinen, Gordon D.; Ensor, Dale D.

    1995-01-01

    An organic extracting solution comprised of a bis(acylpyrazolone or a substituted bis(acylpyrazolone) and an extraction method useful for separating certain elements of the actinide series of the periodic table having a valence of four from one other, and also from one or more of the substances in a group consisting of hexavalent actinides, trivalent actinides, trivalent lanthanides, trivalent iron, trivalent aluminum, divalent metals, and monovalent metals and also from one or more of the substances in a group consisting of hexavalent actinides, trivalent actinides, trivalent lanthanides, trivalent iron, trivalent aluminum, divalent metals, and monovalent metals and also useful for separating hexavalent actinides from one or more of the substances in a group consisting of trivalent actinides, trivalent lanthanides, trivalent iron, trivalent aluminum, divalent metals, and monovalent metals.

  9. Complementary metal ion specificity of the metal-citrate transporters CitM and CitH of Bacillus subtilis

    NARCIS (Netherlands)

    Krom, BP; Warner, JB; Konings, WN; Lolkema, JS; Warner, Jessica B.

    2000-01-01

    Citrate uptake in Bacillus subtilis is stimulated by a wide range of divalent metal ions. The metal ions were separated into two groups based on the expression pattern of the uptake system. The two groups correlated with the metal ion specificity of two homologous B, subtilis secondary citrate

  10. ADSORPTION METHOD FOR SEPARATING METAL CATIONS

    Science.gov (United States)

    Khym, J.X.

    1959-03-10

    The chromatographic separation of fission product cations is discussed. By use of this method a mixture of metal cations containing Zr, Cb, Ce, Y, Ba, and Sr may be separated from one another. Mentioned as preferred exchange adsorbents are resins containing free sulfonic acid groups. Various eluants, such as tartaric acid, HCl, and citric acid, used at various acidities, are employed to effect the selective elution and separation of the various fission product cations.

  11. Metal ion adsorption characteristics of tea leaves

    OpenAIRE

    Takao, Hiromitsu; Kawahigashi, Tatsuo

    2016-01-01

    [Abstract] For effective use of tea leaves, this study experimentally evaluated metal ion adsorption by tea leaves. The experiment described herein was conducted by measuring the ionic solution at a constant density using a fluorescence X-ray device. The metallic ion concentration in the solution and the fluorescence X-ray output intensity showed good correlation. Tea leaves were put into solution adjusted with density of an already-known metallic ion. Then the decrease of the metal ion was m...

  12. SEPARATION OF METAL SALTS BY ADSORPTION

    Science.gov (United States)

    Gruen, D.M.

    1959-01-20

    It has been found that certain metal salts, particularly the halides of iron, cobalt, nickel, and the actinide metals, arc readily absorbed on aluminum oxide, while certain other salts, particularly rare earth metal halides, are not so absorbed. Use is made of this discovery to separate uranium from the rare earths. The metal salts are first dissolved in a molten mixture of alkali metal nitrates, e.g., the eutectic mixture of lithium nitrate and potassium nitrate, and then the molten salt solution is contacted with alumina, either by slurrying or by passing the salt solution through an absorption tower. The process is particularly valuable for the separation of actinides from lanthanum-group rare earths.

  13. Evaluation of a novel PTFE material for separation and preconcentration of trace levels of metal ions in sequential injection (SI) and sequential injection lab-on-valve (SI-LOV) systems interfaced with detection by ETAAS

    DEFF Research Database (Denmark)

    Long, Xiangbao; Chomchoei, Roongrat; Gała, Piotr

    The operational characteristics of a novel PTFE bead material, granular Algoflon®, used for separation and preconcentration of metal ions via adsorption of on-line generated non-charged metal complexes, were evaluated in a sequential injection (SI) system furnished with an external packed column...... and in a sequential injection lab-on-valve (SI-LOV) system. Employed for the determination of cadmium(II), complexed with diethyldithiophosphate (DDPA), and detection by electrothermal atomic absorption spectrometry (ETAAS), its performance was compared to that of a previously used material, Aldrich PTFE, which had...... demonstrated that PTFE was the most promising for solid-state pretreatments. By comparing the two materials, the Algoflon® beads exhibited much higher sensitivity (1.6107 versus 0.2956 μg l-1 per integrated absorbance (s)), and better retention efficiency (82% versus 74%) and enrichment factor (20.8 versus 17...

  14. Application of liquid column chromatography to preconcentration, separation and determination of platinum metals

    International Nuclear Information System (INIS)

    Alimarin, I.P.; Basova, E.M.; Bol'shova, T.A.; Ivanov, V.M.

    1986-01-01

    Separation and determination of platimum metals using the methods of adsorption, ion-pair, ion-exchange, distributing and sieve chromatography are discussed in the review of literature in 1971-1984. Separation and determination of metals as chelates using the method of adsorption and ion-pair chromatograpy are noted to be most perspective directions of developing highly effective liquid chromatography of inorganic systems

  15. Application of ion exchange and extraction chromatography to the separation of actinium from proton-irradiated thorium metal for analytical purposes.

    Science.gov (United States)

    Radchenko, V; Engle, J W; Wilson, J J; Maassen, J R; Nortier, F M; Taylor, W A; Birnbaum, E R; Hudston, L A; John, K D; Fassbender, M E

    2015-02-06

    Actinium-225 (t1/2=9.92d) is an α-emitting radionuclide with nuclear properties well-suited for use in targeted alpha therapy (TAT), a powerful treatment method for malignant tumors. Actinium-225 can also be utilized as a generator for (213)Bi (t1/2 45.6 min), which is another valuable candidate for TAT. Actinium-225 can be produced via proton irradiation of thorium metal; however, long-lived (227)Ac (t1/2=21.8a, 99% β(-), 1% α) is co-produced during this process and will impact the quality of the final product. Thus, accurate assays are needed to determine the (225)Ac/(227)Ac ratio, which is dependent on beam energy, irradiation time and target design. Accurate actinium assays, in turn, require efficient separation of actinium isotopes from both the Th matrix and highly radioactive activation by-products, especially radiolanthanides formed from proton-induced fission. In this study, we introduce a novel, selective chromatographic technique for the recovery and purification of actinium isotopes from irradiated Th matrices. A two-step sequence of cation exchange and extraction chromatography was implemented. Radiolanthanides were quantitatively removed from Ac, and no non-Ac radionuclidic impurities were detected in the final Ac fraction. An (225)Ac spike added prior to separation was recovered at ≥ 98%, and Ac decontamination from Th was found to be ≥ 10(6). The purified actinium fraction allowed for highly accurate (227)Ac determination at analytical scales, i.e., at (227)Ac activities of 1-100 kBq (27 nCi to 2.7 μCi). Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Concentration and separation of trace metals with an arsonic acid resin.

    Science.gov (United States)

    Fritz, J S; Moyers, E M

    1976-08-01

    Macroporeus arsonic acid resins with different pore sizes and surface areas were prepared and the properties compared. One of the resins was used for concentration of trace metal ions from dimineralized water, tap-water, and sea-water. The effect of pH and complexing agents on the recovery of metal ions was studied. A method for separation of uranium(VI) and thorium(IV) from each other and from other metal ions was developed.

  17. A versatile MOF-based trap for heavy metal ion capture and dispersion.

    Science.gov (United States)

    Peng, Yaguang; Huang, Hongliang; Zhang, Yuxi; Kang, Chufan; Chen, Shuangming; Song, Li; Liu, Dahuan; Zhong, Chongli

    2018-01-15

    Current technologies for removing heavy metal ions are typically metal ion specific. Herein we report the development of a broad-spectrum heavy metal ion trap by incorporation of ethylenediaminetetraacetic acid into a robust metal-organic framework. The capture experiments for a total of 22 heavy metal ions, covering hard, soft, and borderline Lewis metal ions, show that the trap is very effective, with removal efficiencies of >99% for single-component adsorption, multi-component adsorption, or in breakthrough processes. The material can also serve as a host for metal ion loading with arbitrary selections of metal ion amounts/types with a controllable uptake ratio to prepare well-dispersed single or multiple metal catalysts. This is supported by the excellent performance of the prepared Pd 2+ -loaded composite toward the Suzuki coupling reaction. This work proposes a versatile heavy metal ion trap that may find applications in the fields of separation and catalysis.

  18. Ion exchange separation of rare earths. I

    International Nuclear Information System (INIS)

    Nghi, Nguyen danh; Matous, K.

    1977-01-01

    The optimal conditions of separating selected rare earths by two ion exchange chromatography using Ostion KS cation exchange resin were studied. The effect of acetic acid concentration in the sorption solution was investigated. The elution process was studied in dependence on the concentration of Na 2 H 2 EDTA, on the total concentration of EDTA 4- ion, on elution agent flow, and on temperature. The optimal conditions were determined by evaluating integral elution curves and changes in acid concentration for systems Y-Pr, La-Pr, Er-Pr, Eu-Pr as follows: The sorption solution requires the presence of Na 2 H 2 EDTA of 0.03M in concentration. The basic elution solution was prepared in the following way: 0.183M Na 2 Mg 2 EDTA, 9.6x10 -3 M Na 2 H 2 EDTA, 3.84x10 -3 M CH 3 COOH, 2.30x10 -2 M CH 3 COONH 4 , 2.30x10 -2 M (NH 4 ) 2 SO 4 . Approximate pH 5.7 to 6.0. The optimal elution solution was prepared by diluting the basic solution so that the total concentration of EDTA 4- equalled 0.075M. The optimal flow was determined to be 0.86 ml.cm -2 .min -1 at a temperature of 55 degC. (author)

  19. Electrically Driven Ion Separations in Permeable Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Bruening, Merlin [Michigan State Univ., East Lansing, MI (United States)

    2017-04-21

    Membranes are attractive for a wide range of separations due to their low energy costs and continuous operation. To achieve practical fluxes, most membranes consist of a thin, selective skin on a highly permeable substrate that provides mechanical strength. Thus, this project focused on creating new methods for forming highly selective ultrathin skins as well as modeling transport through these coatings to better understand their unprecedented selectivities. The research explored both gas and ion separations, and the latter included transport due to concentration, pressure and electrical potential gradients. This report describes a series of highlights of the research and then provides a complete list of publications supported by the grant. These publications have been cited more than 4000 times. Perhaps the most stunning finding is the recent discovery of monovalent/divalent cation and anion selectivities around 1000 when modifying cation- and anion-exchange membranes with polyelectrolyte multilayers (PEMs). This discovery builds on many years of exciting research. (Citation numbers refer to the journal articles in the bibliography.)

  20. Metal-organic frameworks based membranes for liquid separation.

    Science.gov (United States)

    Li, Xin; Liu, Yuxin; Wang, Jing; Gascon, Jorge; Li, Jiansheng; Van der Bruggen, Bart

    2017-11-27

    Metal-organic frameworks (MOFs) represent a fascinating class of solid crystalline materials which can be self-assembled in a straightforward manner by the coordination of metal ions or clusters with organic ligands. Owing to their intrinsic porous characteristics, unique chemical versatility and abundant functionalities, MOFs have received substantial attention for diverse industrial applications, including membrane separation. Exciting research activities ranging from fabrication strategies to separation applications of MOF-based membranes have appeared. Inspired by the marvelous achievements of MOF-based membranes in gas separations, liquid separations are also being explored for the purpose of constructing continuous MOFs membranes or MOF-based mixed matrix membranes. Although these are in an emerging stage of vigorous development, most efforts are directed towards improving the liquid separation efficiency with well-designed MOF-based membranes. Therefore, as an increasing trend in membrane separation, the field of MOF-based membranes for liquid separation is highlighted in this review. The criteria for judicious selection of MOFs in fabricating MOF-based membranes are given. Special attention is paid to rational design strategies for MOF-based membranes, along with the latest application progress in the area of liquid separations, such as pervaporation, water treatment, and organic solvent nanofiltration. Moreover, some attractive dual-function applications of MOF-based membranes in the removal of micropollutants, degradation, and antibacterial activity are also reviewed. Finally, we define the remaining challenges and future opportunities in this field. This Tutorial Review provides an overview and outlook for MOF-based membranes for liquid separations. Further development of MOF-based membranes for liquid separation must consider the demands of strict separation standards and environmental safety for industrial application.

  1. Extraction of complexes of metal ions with pyridine oxyazo compounds

    International Nuclear Information System (INIS)

    Lobanov, F.I.; Nurtaeva, G.K.; Ergozhin, E.E.

    1983-01-01

    Modern state and prospects of the development of investigas tions in the field of extraction of complexes of metal ions (V, In, Cd, Nb, REE, RU, Ta, U, Zr and others) with pyridine oxyazo compoUnds are analyzed. Application of pyridine oxyazo compounds as extraction-photometric reagents is described. Basic methods of oxyazo compounds preparation are considered along with reagent properties and physical-chemical characteristics. Flow diagrams of ion extraction are presented for the above metals. Mechanisms of complexing reactions for metal ions with pyridine oxyazo compounds and stability of forming complexes are considered in detail. Concrete methods of extraction-photometric separation and element determination permitting to find simultaneously several metal ions with similar properties in the case of their joint presence are described

  2. Amorphization of metals by ion implantation and ion beam mixing

    International Nuclear Information System (INIS)

    Rauschenbach, B.; Heera, V.

    1988-01-01

    Amorphous metallic systems can be formed either by high-fluence ion implantation of glassforming species or by irradiation of layered metal systems with inert gas ions. Both techniques and experimental examples are presented. Empirical rules are discussed which predict whether a given system can be transformed into an amorphous phase. Influence of temperature, implantation dose and pre-existing crystalline metal composition on amorphization is considered. Examples are given of the implantation induced amorphous structure, recrystallization and formation of quasicrystalline structures. (author)

  3. Metal Ion Controlled Polymorphism of a Peptide

    DEFF Research Database (Denmark)

    Hemmingsen, Lars Bo Stegeager; Jancso, Attila; Szunyogh, Daniel

    2011-01-01

    , …) in the peptide, and the ligand and structural preferences of the metal ion (in our studies Zn2+, Cd2+, Hg2+, Cu+/2+). Simultaneously, new species such as metal ion bridged ternary complexes or even oligomers may be formed. In recent previous studies we have observed similar polymorphism of zinc finger model...

  4. Metallic Membranes for High Temperature Hydrogen Separation

    DEFF Research Database (Denmark)

    Ma, Y.H.; Catalano, Jacopo; Guazzone, Federico

    2013-01-01

    Composite palladium membranes have extensively been studied in laboratories and, more recently, in small pilot industrial applications for the high temperature separation of hydrogen from reactant mixtures such as water-gas shift (WGS) reaction or methane steam reforming (MSR). Composite Pd...... than 1000, respectively. This chapter describes in detail composite Pd-based membrane preparation methods, which consist of the grading of the support and the deposition of the dense metal layer, their performances, and their applications in catalytic membrane reactors (CMRs) at high temperatures (400...

  5. Metal oxide membranes for gas separation

    Science.gov (United States)

    Anderson, Marc A.; Webster, Elizabeth T.; Xu, Qunyin

    1994-01-01

    A method for permformation of a microporous ceramic membrane onto a porous support includes placing a colloidal suspension of metal oxide particles on one side of the porous support and exposing the other side of the porous support to a drying stream of gas or a reactive gas stream so that the particles are deposited on the drying side of the support as a gel. The gel so deposited can be sintered to form a supported ceramic membrane having mean pore sizes less than 30 Angstroms and useful for ultrafiltration, reverse osmosis, or gas separation.

  6. Supported Molten Metal Membranes for Hydrogen Separation

    Energy Technology Data Exchange (ETDEWEB)

    Datta, Ravindra [Worcester Polytechnic Inst., Worcester, MA (United States). Dept. of Chemical Engineering; Ma, Yi Hua [Worcester Polytechnic Inst., Worcester, MA (United States). Dept. of Chemical Engineering; Yen, Pei-Shan [Worcester Polytechnic Inst., Worcester, MA (United States). Dept. of Chemical Engineering; Deveau, Nicholas [Worcester Polytechnic Inst., Worcester, MA (United States). Dept. of Chemical Engineering; Fishtik, Ilie [Worcester Polytechnic Inst., Worcester, MA (United States). Dept. of Chemical Engineering; Mardilovich, Ivan [Worcester Polytechnic Inst., Worcester, MA (United States). Dept. of Chemical Engineering

    2013-09-30

    We describe here our results on the feasibility of a novel dense metal membrane for hydrogen separation: Supported Molten Metal Membrane, or SMMM. The goal in this work was to develop these new membranes based on supporting thin films of low-melting, non- precious group metals, e.g., tin (Sn), indium (In), gallium (Ga), or their alloys, to provide a flux and selectivity of hydrogen that rivals the conventional but substantially more expensive palladium (Pd) or Pd alloy membranes, which are susceptible to poisoning by the many species in the coal-derived syngas, and further possess inadequate stability and limited operating temperature range. The novelty of the technology presented numerous challenges during the course of this project, however, mainly in the selection of appropriate supports, and in the fabrication of a stable membrane. While the wetting instability of the SMMM remains an issue, we did develop an adequate understanding of the interaction between molten metal films with porous supports that we were able to find appropriate supports. Thus, our preliminary results indicate that the Ga/SiC SMMM at 550 °C has a permeance that is an order of magnitude higher than that of Pd, and exceeds the 2015 DOE target. To make practical SMM membranes, however, further improving the stability of the molten metal membrane is the next goal. For this, it is important to better understand the change in molten metal surface tension and contact angle as a function of temperature and gas-phase composition. A thermodynamic theory was, thus, developed, that is not only able to explain this change in the liquid-gas surface tension, but also the change in the solid-liquid surface tension as well as the contact angle. This fundamental understanding has allowed us to determine design characteristics to maintain stability in the face of changing gas composition. These designs are being developed. For further progress, it is also important to understand the nature of solution and

  7. Complexation ion-exchange chromatography of some metal ions on papers impregnated with Ti(IV)-based inorganic ion exchangers.

    Science.gov (United States)

    Sharma, S D; Gupta, R

    2000-02-01

    The chromatographic behavior of 40 metal ions is studied on titanium (IV) arsenate, titanium (IV) phosphate-, titanium (IV) molybdate-, titanium(IV) tungstate-, and titanium(IV) selenite-impregnated papers in 0.1M oxalic, citric, and tartaric acid as mobile phases. Similar studies are carried out on Whatman No. 1 papers for comparison. The ion-exchange capacity of these papers is determined, and their selectivity for different cations is discussed. The mechanism of migration is explained in terms of ion-exchange, precipitation, and adsorption. The prediction of elution sequence from RF values is also checked. The average Ri is found to be almost linearly dependent on the charge of the metal ions. The effect of the pKa of complexing acids on average RF values of 3d series metal ions is explained. A number of binary and ternary separations are achieved.

  8. Electrochemical ion separation in molten salts

    Energy Technology Data Exchange (ETDEWEB)

    Spoerke, Erik David; Ihlefeld, Jon; Waldrip, Karen; Wheeler, Jill S.; Brown-Shaklee, Harlan James; Small, Leo J.; Wheeler, David R.

    2017-12-19

    A purification method that uses ion-selective ceramics to electrochemically filter waste products from a molten salt. The electrochemical method uses ion-conducting ceramics that are selective for the molten salt cations desired in the final purified melt, and selective against any contaminant ions. The method can be integrated into a slightly modified version of the electrochemical framework currently used in pyroprocessing of nuclear wastes.

  9. Ion separation from dilute electrolyte solutions by nanofiltration

    International Nuclear Information System (INIS)

    Garcia, Corazon M.

    2000-03-01

    Nanofiltration (NF) is a pressure-driven process which is considered potential for the separation of ionic species selectively from solutions containing mixture of electrolyte solutes. The lower operating pressure requirement of NF than reverse osmosis (RO) makes the earlier potentially economical. In the separation of ions, many authors believed that there are membranes with characteristic fixed surface charge and that the mechanism of separation of ions is by the differences in valences of the ions. In this study, experiments involving dilute single-solute and multiple-solute electrolyte solutions were performed using three different NF membranes. Permeate fluxes and ion rejections of the different species of ions in samples of permeate solutions were measured at varied conditions. The mechanism of separation in NF was determined based on the analysis of the trends and behavior of ion rejection relative to the solution temperature, pressure, type of solute, feed concentration and feed solution pH. The results of the experiments show that there is no evidence of the presence of fixed surface charge on the NF membranes. Ion separation was made possible by the combination of sieve effect and ion-hydration effect. Ions having higher hydration numbers showed higher ion rejection than those having lower hydration numbers. A method to determine the effective membrane pore size of NF membranes using hydrodynamic model was proposed. The proposed method is based on the assumptions that the membrane is neutral and that the separation is based on sieving effect. (Author)

  10. A rapid impregnation method for loading desired amounts of extractant on prepacked reversed-phase columns for high performance liquid chromatographic separation of metal ions.

    Science.gov (United States)

    Ramzan, Muhammad; Kifle, Dejene; Wibetoe, Grethe

    2017-06-02

    A time-efficient impregnation method for loading extractant onto reversed-phase columns was developed, using di-(2-ethylhexyl) phosphoric acid (HDEHP) as a model extractant. The optimal loading conditions for the impregnation process of a standard analytical scale column was achieved by dissolving an appropriate amount of HDEHP (per void volume) in n-pentane, flushing the column with two void volumes (5mL) of impregnation solution and heating the column for a short time to remove the solvent. The process takes about one hour, a significant time reduction compared to commonly used impregnation methods (17-23h). The chromatographic traits for separation of the lighter lanthanides (La-Gd) using columns impregnated under different conditions were evaluated; heating for short period of time gave improved column performance most likely due to the presence of n-pentane in the pores of the support material. A linear relation was found (R 2 =0.9934) for the amount of HDEHP loaded as a function of HDEHP concentration in the impregnation solution. The coated amounts of HDEHP were in the range of 0.29-2.25mmol per column by flushing with 5mL of impregnation solution containing 0.3-5.0mmol of HDEHP per void volume. This 'flush-evaporate' impregnation method allowed for loading a pre-determined amount of extractant and produces very small amounts of organic waste. An overview of the various impregnation approaches previously used for extractant coating on prepacked columns and bulk support materials is also presented. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Effective charge of energetic ions in metals

    International Nuclear Information System (INIS)

    Kitagawa, M.; Brandt, W.

    1983-01-01

    The effective charge of energetic ion, as derived from stopping power of metals, is calculated by use of a dielectronic-response function method. The electronic distribution in the ion is described through the variational principle in a statistical approximation. The dependences of effective charge on the ion velocity, atomic number and r/sub s/-value of metal are derived at the low-velocity region. The effective charge becomes larger than the real charge of ion due to the close collisions. We obtain the quasi-universal equation of the fractional effective electron number of ion as a function of the ratio between the ionic size and the minimum distance approach. The comparsion between theoretical and experimental results of the effective charge is performed for the cases of N ion into Au, C and Al. We also discuss the equipartition rule of partially ionized ion at the high-velocity region

  12. Separation of Ni and Co by D2EHPA in the Presence of Citrate Ion

    Science.gov (United States)

    Nadimi, Hamed; Haghshenas Fatmehsari, Davoud; Firoozi, Sadegh

    2017-10-01

    Recycling processes for the recovery of metallic content from the electronic wastes are environmentally friendly and economical. This paper reports a method for the recovery and separation of Ni and Co from the sulfate solution by the use of D2EHPA. In this regard, the influence of citrate ion, as a carboxylate ligand, was examined in the separation conditions of Ni and Co via D2EHPA (a poor selective extractant for Ni and Co separation). It was found that the Δ {pH}_{0.5}^{Ni-Co} (the difference between pH values corresponding to 50 pct extraction of metallic ion) increases to 1.5 at the citrate concentration of 0.05 M; this Δ {pH}_{0.5}^{Ni-Co} value is much higher than that obtained in the absence of citrate ion (0.1). Fourier Transform Infrared Spectroscopy (FT-IR) indicated that the citrate ion is co-absorbed during the metallic ions absorption by D2EHPA meaning that the metal-organic complexes contain Co/Ni and citrate ion. Also, the stoichiometric coefficients of the Ni and Co extraction reaction were proposed by applying the slope analysis method.

  13. Selective heating and separation of isotopes in a metallic plasma

    International Nuclear Information System (INIS)

    Moffa, P.; Cheshire, D.; Flanders, B.; Myer, R.; Robinette, W.; Thompson, J.; Young, S.

    1983-01-01

    Several types of metallic plasmas have been produced at the Plasma Separation Process facility of TRW. Selective heating and separation of specific isotopes in these plasmas have been achieved. In this presentation the authors concentrate on the modeling of the selective heating and separation of the isotope Ni 58 . Two models are currently used to describe the excitation process. In both, the electromagnetic fields in the plasma produced by the ICRH antenna are calculated self-consistently using a kinetic description of the warm plasma dielectric. In the Process Model Code, both the production of the plasma and the heating are calculated using a Monte Carlo approach. Only the excitation process is treated in the second simplified model. Test particles that sample an initial parallel velocity distribution are launched into the heating region and the equations of motion including collisional damping are calculated. For both models, the perpendicular energy for a number of particles with different initial conditions and representing the different isotopes is calculated. This information is then input into a code that models the performance of our isotope separation collector. The motion of the ions of each isotope through the electrically biased collector is followed. An accounting of where each particle is deposited is kept and hence the isotope separation performance of the collector is predicted

  14. Upgraded vacuum arc ion source for metal ion implantation

    International Nuclear Information System (INIS)

    Nikolaev, A. G.; Oks, E. M.; Savkin, K. P.; Yushkov, G. Yu.; Brown, I. G.

    2012-01-01

    Vacuum arc ion sources have been made and used by a large number of research groups around the world over the past twenty years. The first generation of vacuum arc ion sources (dubbed ''Mevva,'' for metal vapor vacuum arc) was developed at Lawrence Berkeley National Laboratory in the 1980s. This paper considers the design, performance parameters, and some applications of a new modified version of this kind of source which we have called Mevva-V.Ru. The source produces broad beams of metal ions at an extraction voltage of up to 60 kV and a time-averaged ion beam current in the milliampere range. Here, we describe the Mevva-V.Ru vacuum arc ion source that we have developed at Tomsk and summarize its beam characteristics along with some of the applications to which we have put it. We also describe the source performance using compound cathodes.

  15. ION EXCHANGE SOFTENING: EFFECTS ON METAL CONCENTRATIONS

    Science.gov (United States)

    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 ...

  16. Separation of palladium from high-level waste using metal ferro cyanide loaded resins

    International Nuclear Information System (INIS)

    Valsala, T.P.; Joseph, Annie; Yeotikar, R.G.

    2005-01-01

    High-level waste (HLW) is generated during reprocessing of spent fuel. HLW contains corrosion products, unextracted actinides, process chemicals and fission products. A recent trend is there to consider waste as a source of wealth. Among the fission products separation and recovery of platinum group metals have gained great attention. HLW is a good source of palladium of the platinum group metal. The present study shows the feasibility of ion exchange separation of Pd from HLW. (author)

  17. Biosorption of Heavy Metal Ions to Brown Algae, Macrocystis pyrifera, Kjellmaniella crassiforia, and Undaria pinnatifida

    OpenAIRE

    Seki, Hideshi; Suzuki, Akira

    1998-01-01

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

  18. Device for separating ruthenium ion from spent fuel material

    International Nuclear Information System (INIS)

    Izumida, Tatsuo; Sasahira, Akira; Ozawa, Yoshihiro; Kawamura, Fumio.

    1988-01-01

    Purpose: To separate plutonium ions efficiently and selectively from organic solvent containing tributyl phosphate used in the main step of reprocessing process. Constitution: The device comprises, as the main constituent factor, a liquid-liquid contact device for bringing not water soluble organic solvent into contact with a nitric acid solution of spent fuel substances and a liquid-liquid contact-separation device for bringing an organic solvent solution containing spent fuel substances separated with nitric acid into contact again with nitric acid. Then, a device is disposed between two liquid-liquid contact devices for staying ruthenium ions and organic solvent for a sufficient time. In this way, ruthenium ions in the organic solvent containing butyl phosphate are gradually converted into complex compounds combined with tributyl phosphate thereby enabling to separate ruthenium ions efficiently and remarkably reduce the corrosion of equipments. (Horiuchi, T.)

  19. Application of pressurized ion exchange to separations of transplutonium elements

    International Nuclear Information System (INIS)

    Campbell, D.O.

    1980-01-01

    High-pressure ion exchange chromatography, used first for nucleic acid separations, was applied to the production of the heavier actinides, particularly the transcurium elements. Its use at the TRU plant is described. Future developments are considered briefly

  20. Metal ions as inflammatory initiators of osteolysis.

    Science.gov (United States)

    Magone, Kevin; Luckenbill, Daniel; Goswami, Tarun

    2015-05-01

    Osteolysis and aseptic loosening currently contribute 75 % of implant failures. Furthermore, with over four million joint replacements projected to be performed in the United States annually, osteolysis and aseptic loosening may continue to pose a significant morbidity. This paper reviews the osteolysis cascade leading to osteoclast activation and bone resorption at the biochemical level. Additionally, the metal ion release mechanism from metallic implants is elucidated. Even though metal ions are not the predominating initiator of osteolysis, they do increase the concentration of key inflammatory cytokines that stimulate osteoclasts and prove to be a contributor to osteolysis and aseptic loosening. Osteolysis is a competitive mechanism among a number of biological reactions, which includes debris release, macrophage and osteoclast activation, an inflammatory response as well as metal ion release. Pharmacological therapy for component loosening has also been reviewed. A non-surgical treatment of osteolysis has not been found in the literature and thus may become an area of future research. Even though this research is warranted, comprehensively understanding the immune response to orthopedic implants and their metallic ions, and thus, creating improved prostheses appears to be the most cost-effective approach to decrease the morbidity related to osteolysis and to design implants with greater longevity. The ionic forms, cytokines, toxicity, gene expression, biological effects, and hypersensitivity responses of metallic elements from metal implants are summarized as well.

  1. Separation and Classification of Lipids Using Differential Ion Mobility Spectrometry

    OpenAIRE

    Shvartsburg, Alexandre A.; Isaac, Giorgis; Leveque, Nathalie; Smith, Richard D.; Metz, Thomas O.

    2011-01-01

    Correlations between the dimensions of a 2-D separation create trend lines that depend on structural or chemical characteristics of the compound class and thus facilitate classification of unknowns. This broadly applies to conventional ion mobility spectrometry (IMS)/mass spectrometry (MS), where the major biomolecular classes (e.g., lipids, peptides, nucleotides) occupy different trend line domains. However, strong correlation between the IMS and MS separations for ions of same charge has im...

  2. Ion beam analysis of metal ion implanted surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Evans, P.J.; Chu, J.W.; Johnson, E.P.; Noorman, J.T. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia); Sood, D.K. [Royal Melbourne Inst. of Tech., VIC (Australia)

    1993-12-31

    Ion implantation is an established method for altering the surface properties of many materials. While a variety of analytical techniques are available for the characterisation of implanted surfaces, those based on particle accelerators such as Rutherford backscattering (RBS) and nuclear reaction analysis (NRA) provide some of the most useful and powerful for this purpose. Application of the latter techniques to metal ion implantation research at ANSTO will be described with particular reference to specific examples from recent studies. Where possible, the information obtained from ion beam analysis will be compared with that derived from other techniques such as Energy Dispersive X-ray (EDX) and Auger spectroscopies. 4 refs., 5 figs.

  3. Chromatography of metal ions with a triazine chelating resin

    Energy Technology Data Exchange (ETDEWEB)

    Wang, W.N.

    1979-05-01

    The synthesis, characterization, and some analytical applications of a new triazine resin are described. Separation of group IB, IIB, VIB, and VIIB metal ions from group VIII metal ions is achieved by this PDT-4 resin. Calcium(II) and magnesium(II) are taken up at pH = 6, 0.1 M acetate and are eluted at pH = 6, 0.1 M sodium nitrate. Copper(II) is retained at pH = 6, 0.1 M acetate and pH = 1 hydrochloric acid and is eluted subsequently by 5 M perchloric acid. Molybdenum(VI) is sorbed selectively from 0.1 N sulfuric acid or hydrochloric acid and is eluted in a tight band by 0.1 N sodium hydroxide. Numerous rapid column chromatographic separations are reported using this new resin, including analysis of NBS standard samples.

  4. Chromatography of metal ions with a triazine chelating resin

    International Nuclear Information System (INIS)

    Wang, W.N.

    1979-05-01

    The synthesis, characterization, and some analytical applications of a new triazine resin are described. Separation of group IB, IIB, VIB, and VIIB metal ions from group VIII metal ions is achieved by this PDT-4 resin. Calcium(II) and magnesium(II) are taken up at pH = 6, 0.1 M acetate and are eluted at pH = 6, 0.1 M sodium nitrate. Copper(II) is retained at pH = 6, 0.1 M acetate and pH = 1 hydrochloric acid and is eluted subsequently by 5 M perchloric acid. Molybdenum(VI) is sorbed selectively from 0.1 N sulfuric acid or hydrochloric acid and is eluted in a tight band by 0.1 N sodium hydroxide. Numerous rapid column chromatographic separations are reported using this new resin, including analysis of NBS standard samples

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  6. Data mining of metal ion environments present in protein structures.

    Science.gov (United States)

    Zheng, Heping; Chruszcz, Maksymilian; Lasota, Piotr; Lebioda, Lukasz; Minor, Wladek

    2008-09-01

    Analysis of metal-protein interaction distances, coordination numbers, B-factors (displacement parameters), and occupancies of metal-binding sites in protein structures determined by X-ray crystallography and deposited in the PDB shows many unusual values and unexpected correlations. By measuring the frequency of each amino acid in metal ion-binding sites, the positive or negative preferences of each residue for each type of cation were identified. Our approach may be used for fast identification of metal-binding structural motifs that cannot be identified on the basis of sequence similarity alone. The analysis compares data derived separately from high and medium-resolution structures from the PDB with those from very high-resolution small-molecule structures in the Cambridge Structural Database (CSD). For high-resolution protein structures, the distribution of metal-protein or metal-water interaction distances agrees quite well with data from CSD, but the distribution is unrealistically wide for medium (2.0-2.5A) resolution data. Our analysis of cation B-factors versus average B-factors of atoms in the cation environment reveals substantial numbers of structures contain either an incorrect metal ion assignment or an unusual coordination pattern. Correlation between data resolution and completeness of the metal coordination spheres is also found.

  7. Laser photodissociation and spectroscopy of mass-separated biomolecular ions

    CERN Document Server

    Polfer, Nicolas C

    2014-01-01

    This lecture notes book presents how enhanced structural information of biomolecular ions can be obtained from interaction with photons of specific frequency - laser light. The methods described in the book ""Laser photodissociation and spectroscopy of mass-separated biomolecular ions"" make use of the fact that the discrete energy and fast time scale of photoexcitation can provide more control in ion activation. This activation is the crucial process producing structure-informative product ions that cannot be generated with more conventional heating methods, such as collisional activation. Th

  8. Electrodialytic separation of alkali-element ions with the aid of ion-exchange membranes

    International Nuclear Information System (INIS)

    Gurskii, V.S.; Moskvin, L.N.

    1988-01-01

    Electrodialytic separation of ions bearing charges of the same sign with the aid of ion-exchange membranes has been examined in the literature in relation to the so-called ideal membranes, which do not exhibit selectivity with respect to one ion type in ion exchange. It has been shown that separation on such membranes is effective only for counterions differing in size of charge. A matter of greater importance from the practical standpoint is the possibility of using electrodialysis for separating ions bearing like charges and having similar properties, including ionic forms of isotopes of the same element. In this paper they report a comparative study of ion separation, with reference to the Cs-Na pair, by electrodialysis through various types of cation-exchange membranes. Changes of the solution concentration in the cathode compartment were monitored by measurement of 22 Na and 137 Cs activities

  9. Chromatographic separations on pyridinium tungstoarsenate-impregnated ion-exchange papers

    International Nuclear Information System (INIS)

    Ion-exchange papers were prepared by impregnating chromatographic Whatman No.3 paper with pyridinium tungstoarsenate exchanger. The composition of the material loaded on the paper shows that the compound has the formula (C 5 H 5 NH) 3 W 12 AsO 40 . Rsub(f) values of 30 metal ions were determined on these ion-exchange papers by developing with ascending technique in solvents containing mixtures of n-propanol and hydrochloric or nitric acid. Several binary, ternary and some quaternary separations were also achieved on these papers. Studies were also made on plain papers for comparison. (author)

  10. Blind Source Separation For Ion Mobility Spectra

    International Nuclear Information System (INIS)

    Marco, S.; Pomareda, V.; Pardo, A.; Kessler, M.; Goebel, J.; Mueller, G.

    2009-01-01

    Miniaturization is a powerful trend for smart chemical instrumentation in a diversity of applications. It is know that miniaturization in IMS leads to a degradation of the system characteristics. For the present work, we are interested in signal processing solutions to mitigate limitations introduced by limited drift tube length that basically involve a loss of chemical selectivity. While blind source separation techniques (BSS) are popular in other domains, their application for smart chemical instrumentation is limited. However, in some conditions, basically linearity, BSS may fully recover the concentration time evolution and the pure spectra with few underlying hypothesis. This is extremely helpful in conditions where non-expected chemical interferents may appear, or unwanted perturbations may pollute the spectra. SIMPLISMA has been advocated by Harrington et al. in several papers. However, more modern methods of BSS for bilinear decomposition with the restriction of positiveness have appeared in the last decade. In order to explore and compare the performances of those methods a series of experiments were performed.

  11. Investigation of electrostatic ion chromatography for the separation of inorganic ions

    OpenAIRE

    Twohill, Eadaoin

    2002-01-01

    The new technique of ‘electrostatic ion chromatography’ (ion chromatography using a zwittenomc stationary phase) has been applied to the separation of ions using pure water as an eluent, without the addition of any inorganic buffers or organic modifiers. The nature of the separation, le cationic or anionic, is dependent upon the nature of the zwittenomc stationary phase. In the work presented here, the zwittenomc surfactant Zwittergent 3-14 was used to functionalise an octadecylsihca stationa...

  12. Ion exchangers as adsorbents for removing metals from aquatic media.

    Science.gov (United States)

    Khan, Meraj A; Bushra, Rani; Ahmad, Anees; Nabi, Syed A; Khan, Dilwar A; Akhtar, Arshia

    2014-02-01

    A polyaniline-based composite cation-exchange material was synthesized by way of sol-gel method and studied to explore its analytical and environmental applications. It was characterized by using instrumental analyses [Fourier transform infrared (spectrometer), X-ray, thermogravimetric analysis/differential thermal analysis, standard electron microscopy, and transmission electron microscopy]. Physicochemical studies, such as ion-exchange capacity, pH titrations, and chemical stability, along with effect of eluent concentration and elution, were also performed to exploit the ion-exchange capabilities. pH titration studies showed that the material presents monofunctional strong cation-exchange behavior. This nanocomposite material is semicrystalline in nature and exhibits improved thermal and chemical stability. The partition coefficient studies of different metal ions in the material were performed in demineralised water and different surfactant media, and it was found to be selective for Pb(II) and Hg(II) ions. To exploit the usefulness of the material as an adsorbent, some important quantitative binary separations of metal ions were performed on polyaniline Zr(IV) molybdophosphate columns. This composite cation exchanger can be applied for the treatment of polluted water to remove heavy metals.

  13. Heavy stable isotope separation by ion cyclotron resonance

    International Nuclear Information System (INIS)

    Louvet, P.; Compant La Fontaine, A.; Larousse, B.; Patris, M.

    1994-01-01

    The scientific feasibility of the ion cyclotron resonance process (ICR), as well as the technical one, has been investigated carefully for light metallic elements, whose masses lies between 40 and 100/1,2/. The present work deals mainly with the same demonstration for heavier elements such as ytterbium, gadolinium and barium. Recent results, as well as future prospects, are considered here. (authors)

  14. Fluorescence signalling of the transition metal ions: Design strategy ...

    Indian Academy of Sciences (India)

    on fluorescence signalling systems for the transition metal ions. It is shown that even simple fluorophore-spacer-receptor systems can display excellent off-on fluorescence signalling towards the quenching metal ions when the fluorophore ...

  15. Separation of plutonium oxidation states by ion chromatography

    International Nuclear Information System (INIS)

    Kim, Seung Soo; Jun, Kwan Sik; Kang, Chul Hyung

    2001-01-01

    The ion chromatography for the separation of plutonium species which are suggested to be Pu 3+ , Pu 4+ PuO 2 + and PuO 2 2+ in natural water was studied. Two separation methods were performed; 1) two-column method containing each of SiO - and SiO-SO 3 - cation exchanger, 2) IC with an AG11 column and the eluent of oxalate/nitric acid. Separation conditions for Eu 3+ , Th 4+ , NpO 2 + and UO 2 2+ in place of plutonium species were acquired from preliminary tests. When these conditions were applied to separate the plutonium species, two-column method was separated them successfully. However, the IC method with oxalate eluent was difficult in the separation of plutonium species due to the change of Pu 3+ and PuO 2 2+ to Pu 4+ and PuO 2 + , respectively. (author)

  16. Polyatomic ions from a high current ion implanter driven by a liquid metal ion source

    Science.gov (United States)

    Pilz, W.; Laufer, P.; Tajmar, M.; Böttger, R.; Bischoff, L.

    2017-12-01

    High current liquid metal ion sources are well known and found their first application as field emission electric propulsion thrusters in space technology. The aim of this work is the adaption of such kind of sources in broad ion beam technology. Surface patterning based on self-organized nano-structures on, e.g., semiconductor materials formed by heavy mono- or polyatomic ion irradiation from liquid metal (alloy) ion sources (LMAISs) is a very promising technique. LMAISs are nearly the only type of sources delivering polyatomic ions from about half of the periodic table elements. To overcome the lack of only very small treated areas by applying a focused ion beam equipped with such sources, the technology taken from space propulsion systems was transferred into a large single-end ion implanter. The main component is an ion beam injector based on high current LMAISs combined with suited ion optics allocating ion currents in the μA range in a nearly parallel beam of a few mm in diameter. Different types of LMAIS (needle, porous emitter, and capillary) are presented and characterized. The ion beam injector design is specified as well as the implementation of this module into a 200 kV high current ion implanter operating at the HZDR Ion Beam Center. Finally, the obtained results of large area surface modification of Ge using polyatomic Bi2+ ions at room temperature from a GaBi capillary LMAIS will be presented and discussed.

  17. The role of metal ion-ligand interactions during divalent metal ion adsorption.

    Science.gov (United States)

    Eldridge, Daniel S; Crawford, Russell J; Harding, Ian H

    2015-09-15

    A suite of seven different divalent metal ions (Ca(II), Cd(II), Cu(II), Mg(II), Ni(II), Pb(II), Zn(II)) was adsorbed from solution onto two Fe2O3 samples, quartz SiO2 and three different amphoteric polystyrene latices (containing amine and carboxyl functional groups). For the metal oxides, a high correlation was observed between the pH at which 50% of the metal was removed from solution (pH50) and the first hydrolysis constant for the metal ion (pK1). For the polystyrene latices, a much higher correlation was observed between the pH50 and pKc (equilibrium constant describing metal-carboxyl affinity) as opposed to pK1. These observations provide evidence of a strong relationship that exists between a metal's affinity for a particular ligand in solution and for that metal ion's affinity for the same ligand present as part of an adsorbing surface. The isoelectric point of the amphoteric latex surface can be increased by decreasing the carboxyl content of the latex surface. For all 7 metal ions, this resulted in a substantial decrease, for any given pH, in adsorption. We suggest that this may be partly due to the decreased carboxyl content, but is dominantly attributable to the presence of less favorable electrostatic conditions. This, in turn, demonstrates that electrostatics play a controlling role in metal ion adsorption onto amphoteric latex surfaces and, in addition to the nature of the metal ion, also controls the pH at which adsorption takes place. Crown Copyright © 2015. Published by Elsevier Inc. All rights reserved.

  18. Three Metal Ions Participate in the Reaction Catalyzed by T5 Flap Endonuclease*S⃞

    Science.gov (United States)

    Syson, Karl; Tomlinson, Christopher; Chapados, Brian R.; Sayers, Jon R.; Tainer, John A.; Williams, Nicholas H.; Grasby, Jane A.

    2008-01-01

    Protein nucleases and RNA enzymes depend on divalent metal ions to catalyze the rapid hydrolysis of phosphate diester linkages of nucleic acids during DNA replication, DNA repair, RNA processing, and RNA degradation. These enzymes are widely proposed to catalyze phosphate diester hydrolysis using a “two-metal-ion mechanism.” Yet, analyses of flap endonuclease (FEN) family members, which occur in all domains of life and act in DNA replication and repair, exemplify controversies regarding the classical two-metal-ion mechanism for phosphate diester hydrolysis. Whereas substrate-free structures of FENs identify two active site metal ions, their typical separation of >4 Å appears incompatible with this mechanism. To clarify the roles played by FEN metal ions, we report here a detailed evaluation of the magnesium ion response of T5FEN. Kinetic investigations reveal that overall the T5FEN-catalyzed reaction requires at least three magnesium ions, implying that an additional metal ion is bound. The presence of at least two ions bound with differing affinity is required to catalyze phosphate diester hydrolysis. Analysis of the inhibition of reactions by calcium ions is consistent with a requirement for two viable cofactors (Mg2+ or Mn2+). The apparent substrate association constant is maximized by binding two magnesium ions. This may reflect a metal-dependent unpairing of duplex substrate required to position the scissile phosphate in contact with metal ion(s). The combined results suggest that T5FEN primarily uses a two-metal-ion mechanism for chemical catalysis, but that its overall metallobiochemistry is more complex and requires three ions. PMID:18697748

  19. Separation of ions in acidic solution by capillary electrophoresis

    Energy Technology Data Exchange (ETDEWEB)

    Thornton, Michelle [Iowa State Univ., Ames, IA (United States)

    1997-10-08

    Capillary electrophoresis (CE) is an effective method for separating ionic species according to differences in their electrophoretic mobilities. CE separations of amino acids by direct detection are difficult due to their similar electrophoretic mobilities and low absorbances. However, native amino acids can be separated by CE as cations at a low pH by adding an alkanesulfonic acid to the electrolyte carrier which imparts selectivity to the system. Derivatization is unnecessary when direct UV detection is used at 185 nm. Simultaneous speciation of metal cations such as vanadium (IV) and vanadium (V) can easily be performed without complexation prior to analysis. An indirect UV detection scheme for acidic conditions was also developed using guanidine as the background carrier electrolyte (BCE) for the indirect detection of metal cations. Three chapters have been removed for separate processing. This report contains introductory material, references, and general conclusions. 80 refs.

  20. Heavy metal ion uptake properties of polystyrene-supported ...

    Indian Academy of Sciences (India)

    Metal ion uptake properties of polystyrene-supported chelating polymer resins functionalized with (i) glycine, (ii) hydroxy benzoic acid, (iii) Schiff base and (iv) diethanol amine have been investigated. The effects of pH, time and initial concentration on the uptake of metal ions have been studied. The uptake of metal ion ...

  1. Engineering of microorganisms towards recovery of rare metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Kuroda, Kouichi; Ueda, Mitsuyoshi [Kyoto Univ. (Japan). Div. of Applied Life Sciences

    2010-06-15

    The bioadsorption of metal ions using microorganisms is an attractive technology for the recovery of rare metal ions as well as removal of toxic heavy metal ions from aqueous solution. In initial attempts, microorganisms with the ability to accumulate metal ions were isolated from nature and intracellular accumulation was enhanced by the overproduction of metal-binding proteins in the cytoplasm. As an alternative, the cell surface design of microorganisms by cell surface engineering is an emerging strategy for bioadsorption and recovery of metal ions. Cell surface engineering was firstly applied to the construction of a bioadsorbent to adsorb heavy metal ions for bioremediation. Cell surface adsorption of metal ions is rapid and reversible. Therefore, adsorbed metal ions can be easily recovered without cell breakage, and the bioadsorbent can be reused or regenerated. These advantages are suitable for the recovery of rare metal ions. Actually, the cell surface display of a molybdate-binding protein on yeast led to the enhanced adsorption of molybdate, one of the rare metal ions. An additional advantage is that the cell surface display system allows high-throughput screening of protein/peptide libraries owing to the direct evaluation of the displayed protein/peptide without purification and concentration. Therefore, the creation of novel metal-binding protein/ peptide and engineering of microorganisms towards the recovery of rare metal ions could be simultaneously achieved. (orig.)

  2. Analysis of Supercritical-Extracted Chelated Metal Ions From Mixed Organic-Inorganic Samples

    Science.gov (United States)

    Sinha, Mahadeva P. (Inventor)

    1996-01-01

    Organic and inorganic contaminants of an environmental sample are analyzed by the same GC-MS instrument by adding an oxidizing agent to the sample to oxidize metal or metal compounds to form metal ions. The metal ions are converted to chelate complexes and the chelate complexes are extracted into a supercritical fluid such as CO2. The metal chelate extract after flowing through a restrictor tube is directly injected into the ionization chamber of a mass spectrometer, preferably containing a refractory metal filament such as rhenium to fragment the complex to release metal ions which are detected. This provides a fast, economical method for the analysis of metal contaminants in a sample and can be automated. An organic extract of the sample in conventional or supercritical fluid solvents can be detected in the same mass spectrometer, preferably after separation in a supercritical fluid chromatograph.

  3. Multiheteromacrocycles that Complex Metal Ions. Sixth Progress Report, 1 May 1979-30 April 1980

    Science.gov (United States)

    Cram, D. J.

    1980-01-15

    Objective is to design synthesize, and evaluate cyclic and polycyclic host organic compounds for their abilities to complex and lipophilize guest metal ions, their complexes, and their clusters. Host organic compounds consist of strategically placed solvating, coordinating, and ion-pairing sites tied together by covalent bonds through hydrocarbon units around cavities shaped to be occupied by guest metal ions or by metal ions plus their ligands. Specificity in complexation is sought by matching the following properties of host and guest: cavity and metal ion sizes; geometric arrangements of binding sites; number of binding sites; character of binding sites; and valences. During this period, hemispherands based on an aryloxy or cyclic urea unit, spherands based on aryloxyl units only, and their complexes with alkali metals and alkaline earths were investigated. An attempt to separate {sup 6}Li and {sup 7}Li by gel permeation chromatography of lithiospherium chloride failed. (DLC)

  4. Melting, solidification, remelting, and separation of glass and metal

    International Nuclear Information System (INIS)

    Ebadian, M.A.; Xin, R.C.; Liu, Y.Z.

    1998-01-01

    Several high-temperature vitrification technologies have been developed for the treatment of a wide range of mixed waste types in both the low-level waste and transuranic (TRU) mixed waste categories currently in storage at DOE sites throughout the nation. The products of these processes are an oxide slag phase and a reduced metal phase. The metal phase has the potential to be recycled within the DOE Complex. Enhanced slag/metal separation methods are needed to support these processes. This research project involves an experimental investigation of the melting, solidification, remelting, and separation of glass and metal and the development of an efficient separation technology. The ultimate goal of this project is to find an efficient way to separate the slag phase from the metal phase in the molten state. This two-year project commenced in October 1995 (FY96). In the first fiscal year, the following tasks were accomplished: (1) A literature review and an assessment of the baseline glass and metal separation technologies were performed. The results indicated that the baseline technology yields a high percentage of glass in the metal phase, requiring further separation. (2) The main melting and solidification system setup was established. A number of melting and solidification tests were conducted. (3) Temperature distribution, solidification patterns, and flow field in the molten metal pool were simulated numerically for the solidification processes of molten aluminum and iron steel. (4) Initial designs of the laboratory-scale DCS and CS technologies were also completed. The principal demonstration separation units were constructed. (5) An application for a patent for an innovative liquid-liquid separation technology was submitted and is pending

  5. Melting, solidification, remelting, and separation of glass and metal

    Energy Technology Data Exchange (ETDEWEB)

    Ebadian, M.A.; Xin, R.C.; Liu, Y.Z.

    1998-01-01

    Several high-temperature vitrification technologies have been developed for the treatment of a wide range of mixed waste types in both the low-level waste and transuranic (TRU) mixed waste categories currently in storage at DOE sites throughout the nation. The products of these processes are an oxide slag phase and a reduced metal phase. The metal phase has the potential to be recycled within the DOE Complex. Enhanced slag/metal separation methods are needed to support these processes. This research project involves an experimental investigation of the melting, solidification, remelting, and separation of glass and metal and the development of an efficient separation technology. The ultimate goal of this project is to find an efficient way to separate the slag phase from the metal phase in the molten state. This two-year project commenced in October 1995 (FY96). In the first fiscal year, the following tasks were accomplished: (1) A literature review and an assessment of the baseline glass and metal separation technologies were performed. The results indicated that the baseline technology yields a high percentage of glass in the metal phase, requiring further separation. (2) The main melting and solidification system setup was established. A number of melting and solidification tests were conducted. (3) Temperature distribution, solidification patterns, and flow field in the molten metal pool were simulated numerically for the solidification processes of molten aluminum and iron steel. (4) Initial designs of the laboratory-scale DCS and CS technologies were also completed. The principal demonstration separation units were constructed. (5) An application for a patent for an innovative liquid-liquid separation technology was submitted and is pending.

  6. Process for the displacement of cyanide ions from metal-cyanide complexes

    Science.gov (United States)

    Smith, Barbara F.; Robinson, Thomas W.

    1997-01-01

    The present invention relates to water-soluble polymers and the use of such water-soluble polymers in a process for the displacement of the cyanide ions from the metal ions within metal-cyanide complexes. The process waste streams can include metal-cyanide containing electroplating waste streams, mining leach waste streams, mineral processing waste streams, and related metal-cyanide containing waste streams. The metal ions of interest are metals that give very strong complexes with cyanide, mostly iron, nickel, and copper. The physical separation of the water-soluble polymer-metal complex from the cyanide ions can be accomplished through the use of ultrafiltration. Once the metal-cyanide complex is disrupted, the freed cyanide ions can be recovered for reuse or destroyed using available oxidative processes rendering the cyanide nonhazardous. The metal ions are released from the polymer, using dilute acid, metal ion oxidation state adjustment, or competing chelating agents, and collected and recovered or disposed of by appropriate waste management techniques. The water-soluble polymer can then be recycled. Preferred water-soluble polymers include polyethyleneimine and polyethyleneimine having a catechol or hydroxamate group.

  7. Activation of Methane by Gaseous Metal Ions

    Czech Academy of Sciences Publication Activity Database

    Schröder, Detlef

    2010-01-01

    Roč. 49, č. 5 (2010), s. 850-851 ISSN 1433-7851 Grant - others:European Research Council(XE) AdG HORIZOMS Institutional research plan: CEZ:AV0Z40550506 Keywords : C-C coupling * C-H bond activation * gas-phase reactions * metal ions * methane Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 12.730, year: 2010

  8. Validation of ion chromatography for the determination of transition metal ions along with alkali, alkaline earth metal elements for uranium oxide fuel

    International Nuclear Information System (INIS)

    Kelkar, Anoop; Prakash, Amrit; Afzal, Mohd.; Panakkal, J.P.

    2009-02-01

    The present report describes the use of Ion chromatography (IC) methods with spectrophotometric and direct conductivity detection for the determination of transition metal elements and alkali alkaline earth metal ions in UO 2 pellets. Transmet analytical column and Metrosep- cation 1-2 column were used for the separation of transition metal elements and alkali and alkaline earth metal elements respectively. Oxalic acid and mixture of pyridine 2,6-dicarboxylic acid (PDCA), Na 2 SO 4 and NaCl were used as mobile phase for the separation of transition metal ions and monitored after post - column reaction with 4,2-pyridylazo resorcinol (PAR) at 520nm spectrophotometrically. In the determination of alkali and alkaline earth metal ions the interference of transition metals are removed by complexing them with PDCA. Mixture of tartaric acid and PDCA employed in the separation of alkali and alkaline earth metal ions and monitored on direct conductivity detector. Mobile phase composition was optimised for the base line separation. Calibration plots of Fe 3+ , Cu 2+ , Ni 2+ , Co 2+ , Cd 2+ , Mn 2+ , Li + , Na + , K + , Mg 2+ , Ca 2+ and Sr 2+ were linear over a wide dynamic range with regression coefficient better than 0.999. Detection limit of above ions were between 5-30ppb. To prevent the overloading of the cation exchange column, uranium matrix was removed from UO 2 sample by solvent extraction with 30% TBP - TOPO/CCl 4 . Ten sintered UO2 pellets of same lot were analysed and R.S.D. ±10% was obtained. These methods were validated by analysis of ILCE standards of UO 2 . (author)

  9. IDENTIFICATION OF CATALYTIC METAL ION LIGANDS IN RIBOZYMES

    Science.gov (United States)

    Frederiksen, John K.; Piccirilli, Joseph A.

    2012-01-01

    Site-bound metal ions participate in the catalytic mechanisms of many ribozymes. Understanding these mechanisms therefore requires knowledge of the specific ligands on both substrate and ribozyme that coordinate these catalytic metal ions. A number of different structural and biochemical strategies have been developed and refined for identifying metal ion binding sites within ribozymes, and for assessing the catalytic contributions of the metal ions bound at those sites. We review these approaches and provide examples of their application, focusing in particular on metal ion rescue experiments and their roles in the construction of the transition state models for the Tetrahymena group I and RNase P ribozymes. PMID:19651216

  10. Ion-induced effects on metallic nanoparticles

    International Nuclear Information System (INIS)

    Klimmer, Andreas

    2010-01-01

    This work deals with the ion-irradiation of metallic nanoparticles in combination with various substrates. Particle diameters were systematically varied within the range of 2.5-14 nm, inter-particle distances range from 30-120 nm. Irradiations were performed with various inert gas ions with energies of 200 keV, resulting in an average ion range larger than the particle dimensions and therefore the effects of irradiation are mainly due to creation of structural defects within the particles and the underlying substrate as well. The main part of this work deals with ion-induced burrowing of metallic nanoparticles into the underlying substrate. The use of micellar nanoparticles with sharp size distribution combined with AFM and TEM analysis allows a much more detailed look at this effect than other works on that topic so far. With respect to the particle properties also a detailed look on the effect of irradiation on the particle structure would be interesting, which might lead to a deliberate influence on magnetic properties, for example. Within the context of this work, first successful experiments were performed on FePt particles, showing a significant reduction of the ordering temperature leading to the magnetically interesting, ordered L1 0 phase. (orig.)

  11. Separation of matrix alloy and reinforcement from aluminum metal ...

    Indian Academy of Sciences (India)

    TECS

    Separation of matrix alloy and reinforcements from pure Al–SiCp composite scrap by salt flux addi- tion has been theoretically predicted .... zero and the salt fluxes have only little solubility in the matrix metal, separation of the matrix ... aluminum melt with SiC at this temperature did not exceed. 30 min. In order to change the ...

  12. Transparent monolithic metal ion containing nanophase aerogels

    Energy Technology Data Exchange (ETDEWEB)

    Risen, W. M., Jr.; Hu, X.; Ji, S.; Littrell, K.

    1999-12-01

    The formation of monolithic and transparent transition metal containing aerogels has been achieved through cooperative interactions of high molecular weight functionalized carbohydrates and silica precursors, which strongly influence the kinetics of gelation. After initial gelation, subsequent modification of the ligating character of the system, coordination of the group VIII metal ions, and supercritical extraction afford the aerogels. The structures at the nanophase level have been probed by photon and electron transmission and neutron scattering techniques to help elucidate the basis for structural integrity together with the small entity sizes that permit transparency in the visible range. They also help with understanding the chemical reactivities of the metal-containing sites in these very high surface area materials. These results are discussed in connection with new reaction studies.

  13. Alkali metal ion templated transition metal formate framework materials: synthesis, crystal structures, ion migration, and magnetism.

    Science.gov (United States)

    Eikeland, Espen; Lock, Nina; Filsø, Mette; Stingaciu, Marian; Shen, Yanbin; Overgaard, Jacob; Iversen, Bo Brummerstedt

    2014-10-06

    Four transition metal formate coordination polymers with anionic frameworks, namely, Na[Mn(HCOO)3], K[Mn(HCOO)3], Na2[Cu3(HCOO)8], and K2[Cu5(HCOO)12], were synthesized using a mild solution chemistry approach. Multitemperature single-crystal (100-300 K) and powder X-ray diffraction studies of the compounds reveal structures of large diversity ranging from cubic chiral Na-Mn formate to triclinic Na-Cu formate. The structural variety is caused by the nature of the transition metals, the alkali metal ion templation, and the versatility of the formate group, which offers metal-metal coordination through three different O-C-O bridging modes (syn-syn, syn-anti, anti-anti) in addition to metal-metal bridging via a single oxygen atom. The two manganese(II) compounds contain mononuclear, octahedrally coordinated moieties, but the three-dimensional connectivity between the manganese octahedra is very different in the two structures. The two copper frameworks, in contrast, consist of binuclear and mononuclear moieties (Na-Cu formate) and trinuclear and mononuclear moieties (K-Cu formate), respectively. Procrystal electron density analysis of the compounds indicates one-dimensional K(+)-ion conductivity in K-Mn and K-Cu, and the nature of the proposed potassium ion migration is compared with results from similar analysis on known Na(+) and K(+) ion conductors. K-Mn and Na-Mn were tested as cathode materials, but this resulted in poor reversibility due to low conductivity or structural collapse. The magnetic properties of the compounds were studied by vibrating sample magnetometric measurements, and their thermal stabilities were determined by thermogravimetric analysis and differential thermal analysis. Despite structural differences, the metal formates that contain the same transition metal have similar magnetic properties and thermal decomposition pathways, that is, the nature of the transition metal controls the compound properties.

  14. THE ROLES OF METAL IONS IN REGULATION BY RIBOSWITCHES

    OpenAIRE

    Ferré-D'Amaré, Adrian; Winkler, Wade C.

    2011-01-01

    Metal ions are required by all organisms in order to execute an array of essential molecular functions. They play a critical role in many catalytic mechanisms and structural properties. Proper homeostasis of ions is critical; levels that are aberrantly low or high are deleterious to cellular physiology. To maintain stable intracellular pools, metal ion-sensing regulatory (metalloregulatory) proteins couple metal ion concentration fluctuations with expression of genes encoding for cation trans...

  15. Separation and classification of lipids using differential ion mobility spectrometry.

    Science.gov (United States)

    Shvartsburg, Alexandre A; Isaac, Giorgis; Leveque, Nathalie; Smith, Richard D; Metz, Thomas O

    2011-07-01

    Correlations between the dimensions of a 2-D separation create trend lines that depend on structural or chemical characteristics of the compound class and thus facilitate classification of unknowns. This broadly applies to conventional ion mobility spectrometry (IMS)/mass spectrometry (MS), where the major biomolecular classes (e.g., lipids, peptides, nucleotides) occupy different trend line domains. However, strong correlation between the IMS and MS separations for ions of same charge has impeded finer distinctions. Differential IMS (or FAIMS) is generally less correlated to MS and thus could separate those domains better. We report the first observation of chemical class separation by trend lines using FAIMS, here for lipids. For lipids, FAIMS is indeed more independent of MS than conventional IMS, and subclasses (such as phospho-, glycero-, or sphingolipids) form distinct, often non-overlapping domains. Even finer categories with different functional groups or degrees of unsaturation are often separated. As expected, resolution improves in He-rich gases: at 70% He, glycerolipid isomers with different fatty acid positions can be resolved. These results open the door for application of FAIMS to lipids, particularly in shotgun lipidomics and targeted analyses of bioactive lipids.

  16. Metal separations using aqueous biphasic partitioning systems

    International Nuclear Information System (INIS)

    Chaiko, D.J.; Zaslavsky, B.; Rollins, A.N.; Vojta, Y.; Gartelmann, J.; Mego, W.

    1996-01-01

    Aqueous biphasic extraction (ABE) processes offer the potential for low-cost, highly selective separations. This countercurrent extraction technique involves selective partitioning of either dissolved solutes or ultrafine particulates between two immiscible aqueous phases. The extraction systems that the authors have studied are generated by combining an aqueous salt solution with an aqueous polymer solution. They have examined a wide range of applications for ABE, including the treatment of solid and liquid nuclear wastes, decontamination of soils, and processing of mineral ores. They have also conducted fundamental studies of solution microstructure using small angle neutron scattering (SANS). In this report they review the physicochemical fundamentals of aqueous biphase formation and discuss the development and scaleup of ABE processes for environmental remediation

  17. Local coordination of polyvalent metal ions in molten halide mixtures

    International Nuclear Information System (INIS)

    Akdeniz, Z.; Tosi, M.P.

    1989-07-01

    Ample experimental evidence is available in the literature on the geometry and the stability of local coordination for polyvalent metal ions in molten mixtures of their halides with alkali halides. Recent schemes for classifying this evidence are discussed. Dissociation of tetrahedral halocomplexes in good ionic systems can be viewed as a classical Mott problem of bound-state stability in a conducting matrix. More generally, structural coordinates can be constructed from properties of the component elements, to separate out systems with long-lived fourfold or sixfold coordination and to distinguish between these. (author). 11 refs, 1 fig

  18. Separating and recycling metals from mixed metallic particles of crushed electronic wastes by vacuum metallurgy.

    Science.gov (United States)

    Zhan, Lu; Xu, Zhenming

    2009-09-15

    During the treatment of electronic wastes, a crushing process is usually used to strip metals from various base plates. Several methods have been applied to separate metals from nonmetals. However, mixed metallic particles obtained from these processes are still a mixture of various metals, including some toxic heavy metals such as lead and cadmium. With emphasis on recovering copper and other precious metals, there have hitherto been no satisfactory methods to recover these toxic metals. In this paper, the criterion of separating metals from mixed metallic particles by vacuum metallurgy is built. The results show that the metals with high vapor pressure have been almost recovered completely, leading to a considerable reduction of environmental pollution. In addition, the purity of copper in mixed particles has been improved from about 80 wt % to over 98 wt %.

  19. The evolution of heavy ion recoil and fragment separators

    International Nuclear Information System (INIS)

    Nole, J.

    1991-01-01

    Research in heavy ion nuclear science is evolving towards more extensive use of reaction recoil and fragment separators. The emphasis has been on the development of devices which promptly separate reaction products according to A or A/q at or very near zero degrees. Probably the most important performance criterion for such devices is the degree to which weak reaction products are separated from the beam and other abundant species. Another important design consideration is the optimization for the beam and reaction product energy or rigidity and the related dominant reaction mechanisms. Separator configuration and size requirements vary rapidly as the research emphasis changes from fission fragments, to slow fusion products (light beam on heavy target), to fast fusion products (heavy on light), to deep ineslastic, and finally to fragmentation products at 50 to 500 MeV per nucleon. Examples of on-going and new research programs with such devices around the world will be discussed along with plans for nearly-completed and recently-designed facilities at several heavy ion labs

  20. Continuous ion exchange separation of zirconium and hafnium

    International Nuclear Information System (INIS)

    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

  1. Development of long-lived radionuclide partitioning technology - Preparation of ion exchanges for selective separation of radioactive elements

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Si Joong; Jeong, Hae In; Shim, Min Sook [Korea University, Seoul (Korea, Republic of); Kim, Jeong [Seonam University, Namwon (Korea, Republic of)

    1995-07-01

    Ion exchanger contained nitrogen-oxygen donor macrocyclic units was synthesized, and immobilization process was carried out by adsorption of the exchanger to silica gel. The binding constants were measured with acid concentration. From the binding constants, selectivity for Pt(II) ion and acid concentration of eluents were determined. The most optimum conditions for the separation were also determined from investigating the effects of amount of immobile phase and column length. And liarit aza-crown ethers were synthesized and selectively separated Cs/Sr ion from mixed metal solution. 37= refs., 24 tabs., 40 figs. (author)

  2. Heavy metal ion uptake properties of polystyrene-supported ...

    Indian Academy of Sciences (India)

    Unknown

    at pH 6 they are found to be Cd(II) and Cr(VI) selective. Metal ion uptake properties of resins follow Freundlich's equation. The resins are recyclable and are therefore employed for the removal of heavy metal pollutants from industrial waste water. Keywords. Uptake properties; heavy metal ion; selectivity; recyclability. 1.

  3. Systems and methods for producing metal clusters; functionalized surfaces; and droplets including solvated metal ions

    Science.gov (United States)

    Cooks, Robert Graham; Li, Anyin; Luo, Qingjie

    2017-08-01

    The invention generally relates to systems and methods for producing metal clusters; functionalized surfaces; and droplets including solvated metal ions. In certain aspects, the invention provides methods that involve providing a metal and a solvent. The methods additionally involve applying voltage to the solvated metal to thereby produce solvent droplets including ions of the metal containing compound, and directing the solvent droplets including the metal ions to a target. In certain embodiments, once at the target, the metal ions can react directly or catalyze reactions.

  4. Process to separate alkali metal salts from alkali metal reacted hydrocarbons

    Science.gov (United States)

    Gordon, John Howard; Alvare, Javier; Larsen, Dennis; Killpack, Jeff

    2017-06-27

    A process to facilitate gravimetric separation of alkali metal salts, such as alkali metal sulfides and polysulfides, from alkali metal reacted hydrocarbons. The disclosed process is part of a method of upgrading a hydrocarbon feedstock by removing heteroatoms and/or one or more heavy metals from the hydrocarbon feedstock composition. This method reacts the oil feedstock with an alkali metal and an upgradant hydrocarbon. The alkali metal reacts with a portion of the heteroatoms and/or one or more heavy metals to form an inorganic phase containing alkali metal salts and reduced heavy metals, and an upgraded hydrocarbon feedstock. The inorganic phase may be gravimetrically separated from the upgraded hydrocarbon feedstock after mixing at a temperature between about 350.degree. C. to 400.degree. C. for a time period between about 15 minutes and 2 hours.

  5. Ion mobility studies of carbohydrates as group I adducts: isomer specific collisional cross section dependence on metal ion radius.

    Science.gov (United States)

    Huang, Yuting; Dodds, Eric D

    2013-10-15

    Carbohydrates play numerous critical roles in biological systems. Characterization of oligosaccharide structures is essential to a complete understanding of their functions in biological processes; nevertheless, their structural determination remains challenging in part due to isomerism. Ion mobility spectrometry provides the means to resolve gas phase ions on the basis of their shape-to-charge ratios, thus providing significant potential for separation and differentiation of carbohydrate isomers. Here, we report on the determination of collisional cross sections for four groups of isomeric carbohydrates (including five isomeric disaccharides, four isomeric trisaccharides, two isomeric pentasaccharides, and two isomeric hexasaccharides) as their group I metal ion adducts (i.e., [M + Li](+), [M + Na](+), [M + K](+), [M + Rb](+), and [M + Cs](+)). In all, 65 collisional cross sections were measured, the great majority of which have not been previously reported. As anticipated, the collisional cross sections of the carbohydrate metal ion adducts generally increase with increasing metal ion radius; however, the collisional cross sections were found to scale with the group I cation size in isomer specific manners. Such measurements are of substantial analytical value, as they illustrate how the selection of charge carrier influences carbohydrate ion mobility determinations. For example, certain pairs of isomeric carbohydrates assume unique collisional cross sections upon binding one metal ion, but not another. On the whole, these data suggest a role for the charge carrier as a probe of carbohydrate structure and thus have significant implications for the continued development and application of ion mobility spectrometry for the distinction and resolution of isomeric carbohydrates.

  6. The isotope separation by ion exchange chromatography. Application to the lithium isotopes separation

    International Nuclear Information System (INIS)

    Albert, M.G.; Barre, Y.; Neige, R.

    1993-01-01

    In this work is described the used study step to demonstrate the industrial feasibility of a lithium isotopes separation process by ion exchange chromatography. After having recalled how is carried out the exchange reaction between the lithium isotopes bound on the cations exchanger resin and those which are in solution and gave the ion exchange chromatography principle, the authors establish a model which takes into account the cascade theory already used for enriched uranium production. The size parameters of this model are: the isotopic separation factor (which depends for lithium of the ligands nature and of the coordination factor), the isotopic exchange kinetics and the mass flow (which depends of the temperature, the lithium concentration, the resins diameter and the front advance). The way they have to be optimized and the implementation of the industrial process are given. (O.M.)

  7. [Metal ion concentrations in patients with metal-metal bearings in prostheses].

    Science.gov (United States)

    Kretzer, J P; Van Der Straeten, C; Sonntag, R; Müller, U; Streit, M; Moradi, B; Jäger, S; Reinders, J

    2013-08-01

    Increased wear leads to elevated systemic and local metal ion concentrations for patients treated with metal-on-metal bearings. The local metal ion content in the close environment of the joint replacement (e.g. joint aspirate or tissue) is several times higher compared to the systemic metal content (e.g. in blood or serum). As a result of increased metal ion levels, local and systemic effects, such as osteolysis, pseudotumors, sensitization or in rare cases toxicity may occur. Although the definition of a specific threshold to define clinical problems is difficult due to a lack of sensitivity, the systemic metal concentration is frequently measured clinically. Currently a threshold for cobalt and chromium between 4 µg/l and 7 µg/l is under debate. Very high levels (≥ 20 µg/l) or a steady increase over time should be a warning sign; however, metal ion levels should not be interpreted as a single diagnostic tool but rather in the entire context of the clinical, radiological and cross-sectional imaging, metal artefact reduction sequence (MARS) magnetic resonance imaging (MRI), ultrasound and computed tomography (CT) findings.

  8. The roles of metal ions in regulation by riboswitches.

    Science.gov (United States)

    Ferré-D'Amaré, Adrian R; Winkler, Wade C

    2011-01-01

    Metal ions are required by all organisms in order to execute an array of essential molecular functions. They play a critical role in many catalytic mechanisms and structural properties. Proper homeostasis of ions is critical; levels that are aberrantly low or high are deleterious to cellular physiology. To maintain stable intracellular pools, metal ion-sensing regulatory (metalloregulatory) proteins couple metal ion concentration fluctuations with expression of genes encoding for cation transport or sequestration. However, these transcriptional-based regulatory strategies are not the only mechanisms by which organisms coordinate metal ions with gene expression. Intriguingly, a few classes of signal-responsive RNA elements have also been discovered to function as metalloregulatory agents. This suggests that RNA-based regulatory strategies can be precisely tuned to intracellular metal ion pools, functionally akin to metal-loregulatory proteins. In addition to these metal-sensing regulatory RNAs, there is a yet broader role for metal ions in directly assisting the structural integrity of other signal-responsive regulatory RNA elements. In this chapter, we discuss how the intimate physicochemical relationship between metal ions and nucleic acids is important for the structure and function of metal ion- and metabolite-sensing regulatory RNAs.

  9. Metals separation using solvent extractants on magnetic microparticles

    International Nuclear Information System (INIS)

    Nunez, L.; Pourfarzaneh, M.

    1997-01-01

    The magnetically assisted chemical separation program was initially funded by DOE EM-50 to develop processes for the efficient separation of radionuclides and other hazardous metals. This process has simulated the partnership between industry and ANL for many applications related to hazardous metal problems in industry. In-tank or near-tank hazardous metals separation using magnetic particles promises simple, compact processing at very low costs and employs mature chemical separations technologies to remove and recover hazardous metals from aqueous solutions. The selective chemical extractants are attached to inexpensive magnetic carrier particles. Surfaces of small particles composed of rare earths or ferromagnetic materials are treated to retain chemical extractants (e.g., TBP, CMPO, quaternary amines, carboxylic acid). After selective partitioning of contaminants to the surface layer, magnets are used to collect the loaded particles from the tank. The particles can be regenerated by stripping the contaminants and the selective metals can be recovered and recycled from the strip solution. This process and its related equipment are simple enough to be used for recovery/recycling and waste minimization activities at many industrial sites. Both the development of the process for hazardous and radioactive waste and the transfer of the technology will be discussed

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

    International Nuclear Information System (INIS)

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

    1995-01-01

    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. This report describes the process of electrodialysis-ion exchange (EDIX) for treating aqueous wastes streams consisting of nitrates, sodium, organics, heavy metals, and radioactive species

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

    Science.gov (United States)

    Joshi, Ashok V [Salt Lake City, UT; Balagopal, Shekar [Sandy, UT; Pendelton, Justin [Salt Lake City, UT

    2011-12-13

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

  12. Heavy metal ion uptake properties of polystyrene-supported ...

    Indian Academy of Sciences (India)

    Unknown

    concentration on the uptake of metal ions have been studied. The uptake of metal ion depends on pH. The resins are more selective at pH 10 for Pb(II) and Hg(II), whereas at pH 6 they are found to be Cd(II) and Cr(VI) selective. Metal ion uptake properties of resins follow Freundlich's equation. The resins are recyclable and ...

  13. Preferential solvation, ion pairing, and dynamics of concentrated aqueous solutions of divalent metal nitrate salts

    Science.gov (United States)

    Yadav, Sushma; Chandra, Amalendu

    2017-12-01

    We have investigated the characteristics of preferential solvation of ions, structure of solvation shells, ion pairing, and dynamics of aqueous solutions of divalent alkaline-earth metal nitrate salts at varying concentration by means of molecular dynamics simulations. Hydration shell structures and the extent of preferential solvation of the metal and nitrate ions in the solutions are investigated through calculations of radial distribution functions, tetrahedral ordering, and also spatial distribution functions. The Mg2+ ions are found to form solvent separated ion-pairs while the Ca2+ and Sr2+ ions form contact ion pairs with the nitrate ions. These findings are further corroborated by excess coordination numbers calculated through Kirkwood-Buff G factors for different ion-ion and ion-water pairs. The ion-pairing propensity is found to be in the order of Mg(NO3) 2 ions which is achieved in the current study through electronic continuum correction force fields. A detailed analysis of the effects of ion-pairs on the structure and dynamics of water around the hydrated ions is done through classification of water into different subspecies based on their locations around the cations or anions only or bridged between them. We have looked at the diffusion coefficients, relaxation of orientational correlation functions, and also the residence times of different subspecies of water to explore the dynamics of water in different structural environments in the solutions. The current results show that the water molecules are incorporated into fairly well-structured hydration shells of the ions, thus decreasing the single-particle diffusivities and increasing the orientational relaxation times of water with an increase in salt concentration. The different structural motifs also lead to the presence of substantial dynamical heterogeneity in these solutions of strongly interacting ions. The current study helps us to understand the molecular details of hydration structure, ion

  14. Blood metal ion concentrations in metal-on-metal total hip arthroplasty.

    Science.gov (United States)

    Ohtsuru, Tadahiko; Morita, Yuji; Murata, Yasuaki; Shimamoto, Shuji; Munakata, Yutaro; Kato, Yoshiharu

    2017-05-01

    The hip placement with a metal-on-metal (MOM) bearing has been used for both surface replacement and total hip arthroplasty (THA). Use of MOM bearing for hip replacement reduces the wear compared to conventional bearings. We prospectively assessed 30 patients who underwent unilateral MOM THA. A control group of 30 patients who underwent metal-on-polyethylene THA using the implants as the other group, except for bearing, were accessed. Blood samples were collected preoperatively and at 3- , 6- , 9- , 12- , 15- , 18- , and 24-month intervals. Changes in mean blood metal ion concentration were compared between the MOM and metal-on-polyethylene groups. A statistically significant positive correlation was observed between blood cobalt and chromium concentrations in all of the patients. The mean blood ion concentrations of the MOM were significantly higher than those of the metal-on-polyethylene. A statistically significant negative correlation was found between maximum blood cobalt concentration and cup version angle. The maximum blood chromium concentrations in the patients who had larger cup version angles were more likely to decrease. We considered that cup version angle is one of the factors that have the greatest effect on blood metal ion concentration, and the target cup version angle that did not induce an increase in blood metal ion concentrations was approximately 20°.

  15. Plasma immersion ion implantation for reducing metal ion release

    Energy Technology Data Exchange (ETDEWEB)

    Diaz, C.; Garcia, J. A.; Maendl, S.; Pereiro, R.; Fernandez, B.; Rodriguez, R. J. [Centro de Ingenieria Avanzada de Superficies AIN, 31191, Cordovilla-Pamplona (Spain); Leibniz-Institut fuer Oberflaechenmodifizierung, 04318 Leipzig (Germany); Universidad de Oviedo, Departamento Quimica Fisica y Analitica (Spain); Centro de Ingenieria Avanzada de Superficies AIN, 31191, Cordovilla-Pamplona (Spain)

    2012-11-06

    Plasma immersion ion implantation of Nitrogen and Oxygen on CoCrMo alloys was carried out to improve the tribological and corrosion behaviors of these biomedical alloys. In order to optimize the implantation results we were carried experiments at different temperatures. Tribocorrosion tests in bovine serum were used to measure Co, Cr and Mo releasing by using Inductively Coupled Plasma Mass Spectrometry analysis after tests. Also, X-ray Diffraction analysis were employed in order to explain any obtained difference in wear rate and corrosion tests. Wear tests reveals important decreases in rate of more than one order of magnitude for the best treatment. Moreover decreases in metal release were found for all the implanted samples, preserving the same corrosion resistance of the unimplanted samples. Finally this paper gathers an analysis, in terms of implantation parameters and achieved properties for industrial implementation of these treatments.

  16. Backscattering of light ions from metal surfaces

    International Nuclear Information System (INIS)

    Verbeek, H.

    1975-07-01

    When a metal target is bombarded with light ions some are implanted and some are reflected from the surface or backscattered from deeper layers. This results in an energy distribution of the backscattered particles which reaches from zero to almost the primary energy. The number of the backscattered particles and their energy, angular, and charge distributions depends largely on the energy and the ion target combination. For high energies (i.e., greater than50 keV for protons) particles are backscattered in a single collision governed by the Rutherford cross section. Protons and He-ions with energies of 100 keV to several MeV are widely used for thin film analysis. For lower energies multiple collisions and the screening of the Coulomb potential have to be taken into account, which makes the theoretical treatment more difficult. This energy region is, however, of special interest in the field of nuclear fusion research. Some recent results for energies below 20 keV are discussed in some detail. (auth)

  17. Apparatus and Method for Separation of Ions According to Mass

    International Nuclear Information System (INIS)

    A. Fetterman; N. Fisch

    2008-01-01

    This is a device that uses rotating plasma and radiofrequency waves in order to separate ions within the plasma according to their mass. The device fundamentally consists of a mirror configuration (a primarily axial field) with a radial electric field, producing rotation. Radiofrequency waves are injected to produce diffusion paths allowing select species to exit through the loss cone. The use of these waves within the trap maintains the radial electric field, and allows species to be removed at low energy and with precise control over the location of exit

  18. A 1-dodecanethiol-based phase transfer protocol for the highly efficient extraction of noble metal ions from aqueous phase.

    Science.gov (United States)

    Chen, Dong; Cui, Penglei; Cao, Hongbin; Yang, Jun

    2015-03-01

    A 1-dodecanethiol-based phase-transfer protocol is developed for the extraction of noble metal ions from aqueous solution to a hydrocarbon phase, which calls for first mixing the aqueous metal ion solution with an ethanolic solution of 1-dodecanethiol, and then extracting the coordination compounds formed between noble metal ions and 1-dodecanethiol into a non-polar organic solvent. A number of characterization techniques, including inductively coupled plasma atomic emission spectroscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis demonstrate that this protocol could be applied to extract a wide variety of noble metal ions from water to dichloromethane with an efficiency of >96%, and has high selectivity for the separation of the noble metal ions from other transition metals. It is therefore an attractive alternative for the extraction of noble metals from water, soil, or waste printed circuit boards. Copyright © 2015. Published by Elsevier B.V.

  19. Metal-organic frameworks for lithium ion batteries and supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Ke, Fu-Sheng; Wu, Yu-Shan; Deng, Hexiang, E-mail: hdeng@whu.edu.cn

    2015-03-15

    Porous materials have been widely used in batteries and supercapacitors attribute to their large internal surface area (usually 100–1000 m{sup 2} g{sup −1}) and porosity that can favor the electrochemical reaction, interfacial charge transport, and provide short diffusion paths for ions. As a new type of porous crystalline materials, metal-organic frameworks (MOFs) have received huge attention in the past decade due to their unique properties, i.e. huge surface area (up to 7000 m{sup 2} g{sup −1}), high porosity, low density, controllable structure and tunable pore size. A wide range of applications including gas separation, storage, catalysis, and drug delivery benefit from the recent fast development of MOFs. However, their potential in electrochemical energy storage has not been fully revealed. Herein, the present mini review appraises recent and significant development of MOFs and MOF-derived materials for rechargeable lithium ion batteries and supercapacitors, to give a glimpse into these potential applications of MOFs. - Graphical abstract: MOFs with large surface area and high porosity can offer more reaction sites and charge carriers diffusion path. Thus MOFs are used as cathode, anode, electrolyte, matrix and precursor materials for lithium ion battery, and also as electrode and precursor materials for supercapacitors. - Highlights: • MOFs have potential in electrochemical area due to their high porosity and diversity. • We summarized and compared works on MOFs for lithium ion battery and supercapacitor. • We pointed out critical challenges and provided possible solutions for future study.

  20. Prospects for separating heavy metal from contaminated soil

    International Nuclear Information System (INIS)

    Langen, M.; Hoberg, H.; Hamacher, B.

    1994-01-01

    For decades, large quantities of organic and inorganic pollutants have been brought into the soil as a result of the industrial operations of smelting and coking plants. This paper reports on the prospects of separating heavy metals from soil contaminated by smelting and coking plants by means of a physical/chemical washing procedure. Besides the description of virgin soil characteristics, cleaning results and process parameters of calssification, density separation and flotation processes are presented. It is shown that heavy metal pollution of virgin soil can be reduced by the classical process stages of soil washing. The metal content of virgin soil are critically assessed whereby the limits of the physical-chimical washing process will also be entered into. Emphasis is placed on the significance of the determination of limiting values for inorganic contamination, especially for soil contaminated with both organic and inorganic pollution. (orig.) [de

  1. A biosystem for removal of metal ions from water

    Energy Technology Data Exchange (ETDEWEB)

    Kilbane, J.J. II.

    1990-01-01

    The presence of heavy metal ions in ground and surface waters constitutes a potential health risk and is an environmental concern. Moreover, processes for the recovery of valuable metal ions are of interest. Bioaccumulation or biosorption is not only a factor in assessing the environmental risk posed by metal ions; it can also be used as a means of decontamination. A biological system for the removal and recovery of metal ions from contaminated water is reported here. Exopolysaccharide-producing microorganisms, including a methanotrophic culture, are demonstrated to have superior metal binding ability, compared with other microbial cultures. This paper describes a biosorption process in which dried biomass obtained from exopolysaccharide-producing microorganisms is encapsulated in porous plastic beads and is used for metal ion binding and recovery. 22 refs., 13 figs.

  2. Electrospun polyimide-composite separator for lithium-ion batteries

    International Nuclear Information System (INIS)

    Shayapat, Jaritphun; Chung, Ok Hee; Park, Jun Seo

    2015-01-01

    Non-woven mats of thermally stable polyimide (PI) composites were fabricated as a separator of lithium-ion batteries (LIBs) by first electrospinning a mixture of the pre-polymer, poly(amic acid) ammonium salt (PAAS), and inorganic nanoparticles of SiO 2 or Al 2 O 3 and then imidizing the electrospun nanofibers of the PAAS composites at 350 °C. The microstructures of the electrospun PI nanofibers, electrospun PI–SiO 2 -composite nanofibers, electrospun PI–Al 2 O 3 -composite nanofibers, and the commercial separator SV718 were examined using field-emission scanning electron microscopy and transmission electron microscopy. Test results of the thermal properties of the PI nanofibers, PI-composite nanofibers, and SV718, obtained with a thermal gravimetric analyzer and a differential scanning calorimeter, indicate the superior thermal stability of PI and PI composites, which showed no melting peak and no decomposition at 600 °C, while SV718 had a melting peak at 137 °C and decomposed at 300 °C. The thermal stability of the separators, evaluated in a hot-oven test, showed no shrinkage of PI and PI composites at 200 °C, while SV718 started to shrink at above 100 °C. Using a drop of liquid electrolyte on the surface of each separator, the electrolyte contact angle on PI and PI composites was around 10° and that on SV718 was 54°, indicating that PI and PI composites had better wettability than SV718. The porosity and liquid-electrolyte uptake of the PI composites were over 90% and 790%, respectively, while the corresponding values for SV718 were 40% and 101%, respectively, implying that the separators consisting of the non-woven mats of PI–SiO 2 -composite nanofibers and PI–Al 2 O 3 -composite nanofibers had lower interfacial resistance than the commercial SV718 separator. The electrochemical performance of the PI-composite separator assembled between the LiCoO 2 cathode and the Li anode of an LIB exhibited more stable cycle performance, higher discharge

  3. Hierarchical Chitin Fibers with Aligned Nanofibrillar Architectures: A Nonwoven-Mat Separator for Lithium Metal Batteries.

    Science.gov (United States)

    Kim, Joong-Kwon; Kim, Do Hyeong; Joo, Se Hun; Choi, Byeongwook; Cha, Aming; Kim, Kwang Min; Kwon, Tae-Hyuk; Kwak, Sang Kyu; Kang, Seok Ju; Jin, Jungho

    2017-06-27

    Here, we introduce regenerated fibers of chitin (Chiber), the second most abundant biopolymer after cellulose, and propose its utility as a nonwoven fiber separator for lithium metal batteries (LMBs) that exhibits an excellent electrolyte-uptaking capability and Li-dendrite-mitigating performance. Chiber is produced by a centrifugal jet-spinning technique, which allows a simple and fast production of Chibers consisting of hierarchically aligned self-assembled chitin nanofibers. Following the scrutinization on the Chiber-Li-ion interaction via computational methods, we demonstrate the potential of Chiber as a nonwoven mat-type separator by monitoring it in Li-O 2 and Na-O 2 cells.

  4. Separation of non-ferrous metals from ASR by corona electrostatic separation

    Science.gov (United States)

    Kim, Yang-soo; Choi, Jin-Young; Jeon, Ho-Seok; Han, Oh-Hyung; Park, Chul-Hyun

    2016-04-01

    Automotive shredder residue (ASR), the residual fraction of approximate 25% obtained after dismantling and shredding from waste car, consists of polymers (plastics and rubber), metals (ferrous and non-ferrous), wood, glass and fluff (textile and fiber). ASR cannot be effectively separated due to its heterogeneous materials and coated or laminated complexes and then largely deposited in land-fill sites as waste. Thus reducing a pollutant release before disposal, techniques that can improve the liberation of coated (or laminated) complexes and the recovery of valuable metals from the shredder residue are needed. ASR may be separated by a series of physical processing operations such as comminution, air, magnetic and electrostatic separations. The work deals with the characterization of the shredder residue coming from an industrial plant in korea and focuses on estimating the optimal conditions of corona electrostatic separation for improving the separation efficiency of valuable non-ferrous metals such as aluminum, copper and etc. From the results of test, the maximum separation achievable for non-ferrous metals using a corona electrostatic separation has been shown to be recovery of 92.5% at a grade of 75.8%. The recommended values of the process variables, particle size, electrode potential, drum speed, splitter position and relative humidity are -6mm, 50 kV, 35rpm, 20° and less 40%, respectively. Acknowledgments This study was supported by the R&D Center for Valuable Recycling (Global-Top R&BD Program) of the Ministry of Environment. (Project No. GT-11-C-01-170-0)

  5. Separation of seven arsenic species by ion-pair and ion-exchange high performance liquid chromatography

    DEFF Research Database (Denmark)

    Larsen, Erik Huusfeldt; Hansen, Sven Hedegaard

    1992-01-01

    Arsenite, arsenate, monomethylarsonate, dimethylarsinate, arsenobetaine, arsenocholine and the tetramethylarsonium ion were subjected to ion-exchange and ion-pair reversed phase HPLC. The ion exchange method was superior in selectivity and time of analysis for the arsenic anions. The ammonium ions...... used for the ion-pair method only resulted in separation of some of the anionic arsenic compounds. Flame atomic absorption spectrometry was used for on-line arsenic-specific detection....

  6. Ra/Ca separation by ion exchange chromatography

    International Nuclear Information System (INIS)

    Flores Mendoza, J.

    1990-01-01

    Ra/Ca separation by ion exchange. The objective of this work was to acquire knowledge of the chromatographic behaviour of the alkaline earth cations calcium, barium and radium and the obtention of well-defined alpha spectra of 226 Ra. Three cationic ion exchange resins (Dower 50 W-X8, AG 50W-XB and Merck I) and three complexing agents (ethylenediaminetetraacetic acid, citric acid and tartaric acid) at various pH values have been investigated. The three types of ions are fixed on the resins at pH 4.8; calcium is eluted at pH between 5 and 6 depending on the resin; barium and radium are eluted at pH values from 8 to 11. Radium is also eluted with a 2 M nitric acid solution, from which it can be electrodeposited on a stainless steel disk potassium fluoride as electrolyte at pH 14. The electrolysis is conducted for 18 hours with a current of mA. Under these conditions high resolution alpha spectra were obtained for 226 Ra, which was practically free from radioactive contaminants (Author)

  7. Study of Aging ion exchange membranes used in separation processes

    International Nuclear Information System (INIS)

    Bellakhal, N.; Ghalloussi, R.; Dammak, L.

    2009-01-01

    Presently, the most important application of ion exchange membranes (IEM) is the electrodialysis. This technique consists of a membrane separation using a series of anion exchange membranes alternately and cations, often used for the desalination of brackish water. These membranes are confronted with problems of aging. Indeed, the more they are used more physical and chemical properties will change. A comparative study of the behavior of both EMI and new but the same treatment is carried out by measuring a magnitude transfer characteristic: ion permeability. Ionic permeability is a physical quantity can have an idea about the selectivity of the membrane towards the charged species and the p orosity o f the membrane. It is a transport of ions (cations + anions) through the membrane. Thus, determining the ion permeability is to determine the diffusion flux of a strong electrolyte through a membrane separating two compartments (one containing electrolytes and other water initially ultrapure who will gradually electrolyte through the membrane). The measurement technique used is that by conductimetric detection because of the ease of its implementation and its accuracy. Thus, the variation of the concentration of the electrolyte is continuously monitored by measuring the conductivity of the solution diluted with time. The curves s = f (t) MEA and MEC new and used varying concentration of the electrolyte membranes show that let in less waste of strong electrolyte (NaCl and HCl) than new ones. This can be explained by: - The functional sites are combined with polyvalent ions present even in trace amounts in the solution process and become inactive. The membrane loses its hydrophilic character and turns into a film almost hydrophobic. - The chemical attacks and electrodialysis operations have degraded and eliminated much of the fixed sites leading to the same effects on the hydrophilic membrane. - These two assumptions have been reinforced by the extent of exchange

  8. Mound Laboratory activities in chemical and physical research: July--December 1976. [Isotope separation; metal hydride research, separation chemistry and separation research

    Energy Technology Data Exchange (ETDEWEB)

    1977-05-04

    The status of the following programs is reported: isotope separation of carbon, argon, helium, krypton, neon, xenon, oxygen, and sulfur; metal hydride research; separation chemistry; and separation research. (LK)

  9. Recent Advances in Antimicrobial Hydrogels Containing Metal Ions and Metals/Metal Oxide Nanoparticles

    Directory of Open Access Journals (Sweden)

    Fazli Wahid

    2017-11-01

    Full Text Available Recently, the rapid emergence of antibiotic-resistant pathogens has caused a serious health problem. Scientists respond to the threat by developing new antimicrobial materials to prevent or control infections caused by these pathogens. Polymer-based nanocomposite hydrogels are versatile materials as an alternative to conventional antimicrobial agents. Cross-linking of polymeric materials by metal ions or the combination of polymeric hydrogels with nanoparticles (metals and metal oxide is a simple and effective approach for obtaining a multicomponent system with diverse functionalities. Several metals and metal oxides such as silver (Ag, gold (Au, zinc oxide (ZnO, copper oxide (CuO, titanium dioxide (TiO2 and magnesium oxide (MgO have been loaded into hydrogels for antimicrobial applications. The incorporation of metals and metal oxide nanoparticles into hydrogels not only enhances the antimicrobial activity of hydrogels, but also improve their mechanical characteristics. Herein, we summarize recent advances in hydrogels containing metal ions, metals and metal oxide nanoparticles with potential antimicrobial properties.

  10. Coordination of cassava starch to metal ions and thermolysis of ...

    African Journals Online (AJOL)

    Cassava starch formed Werner-type complexes with ions of metals from the transition groups. This was proven by conductivity and electron paramagnetic resonance measurements. The coordination of starch to central metal ions influenced the thermal decomposition of starch. As a rule complexes started to decompose at ...

  11. COORDINATION OF CASSAVA STARCH TO METAL IONS AND ...

    African Journals Online (AJOL)

    a

    ABSTRACT. Cassava starch formed Werner-type complexes with ions of metals from the transition groups. This was proven by conductivity and electron paramagnetic resonance measurements. The coordination of starch to central metal ions influenced the thermal decomposition of starch. As a rule complexes started to ...

  12. Metal ion binding with dehydroannulenes – Plausible two ...

    Indian Academy of Sciences (India)

    WINTEC

    Abstract. Theoretical investigations have been carried out at B3LYP/6-311++G** level of theory to study the binding interaction of various metal ions, Li+, Na+ and K+ with dehydroannulene systems. The present study reveals that alkali metal ions bind strongly to dehydroannulenes and the passage through the central.

  13. Metal ion sequestration: An exciting dimension for molecularly ...

    African Journals Online (AJOL)

    Metal ion sequestration: An exciting dimension for molecularly imprinted polymer technology. DMS Mosha, LL Mkayula. Abstract. The use of a tight binding macrocyclic ligand to complex a metal ion so that this serves as receptee on the Molecularly Imprinted Polymer (MIP) receptor as described here affords a sequestration ...

  14. Interaction of Hydroxyproline with Bivalent Metal Ions in Chemical ...

    African Journals Online (AJOL)

    NICO

    The stability constants of the ML and ML2 complex species of some metal ions, namely beryllium(II) and cobalt(II), with hydroxyproline were ... metal ions have several significant applications in biological systems.3–20 Beryllium is one ... 1 filter paper for chromatography was used for the purpose of electrophoresis. An Elico ...

  15. Chromatography Of Metal Ions On Wood Cellulose Impregnated ...

    African Journals Online (AJOL)

    Adsorption chromatography of some heavy metal ions on wood cellulose of saw dust (wood waste dust) modified with hydrochloric acid, urea and thiourea was studied. Atomic absorption spectrophotometry (AAS) was used to determine the initial concentration of solutions of Zn2+, Cu2+, Ni2+, Pb2+, and Fe3+ metal ions.

  16. In vitro cytotoxicity of metallic ions released from dental alloys

    NARCIS (Netherlands)

    Milheiro, A.; Nozaki, K.; Kleverlaan, C.J.; Muris, J.; Miura, H.; Feilzer, A.J.

    2016-01-01

    The cytotoxicity of a dental alloy depends on, but is not limited to, the extent of its corrosion behavior. Individual ions may have effects on cell viability that are different from metals interacting within the alloy structure. We aimed to investigate the cytotoxicity of individual metal ions in

  17. Fluorescence signalling of the transition metal ions: Design strategy ...

    Indian Academy of Sciences (India)

    Unknown

    Abstract. Transition metal ions are notorious for their fluorescence quenching abilities. In this paper, we discuss the design strategies for the development of efficient off-on fluorescence signalling systems for the transition metal ions. It is shown that even simple fluorophore-spacer-receptor systems can display excellent.

  18. Cesium ion bombardment of metal surfaces

    International Nuclear Information System (INIS)

    Tompa, G.S.

    1986-01-01

    The steady state cesium coverage due to cesium ion bombardment of molybdenum and tungsten was studied for the incident energy range below 500 eV. When a sample is exposed to a positive ion beam, the work function decreases until steady state is reached with a total dose of less than ≅10 16 ions/cm 2 , for both tungsten and molybdenum. A steady state minimum work function surface is produced at an incident energy of ≅100 eV for molybdenum and at an incident energy of ≅45 eV for tungsten. Increasing the incident energy results in an increase in the work function corresponding to a decrease in the surface coverage of cesium. At incident energies less than that giving the minimum work function, the work function approaches that of cesium metal. At a given bombarding energy the cesium coverage of tungsten is uniformly less than that of molybdenum. Effects of hydrogen gas coadsorption were also examined. Hydrogen coadsorption does not have a large effect on the steady state work functions. The largest shifts in the work function due to the coadsorption of hydrogen occur on the samples when there is no cesium present. A theory describing the steady-state coverage was developed is used to make predictions for other materials. A simple sticking and sputtering relationship, not including implantation, cannot account for the steady state coverage. At low concentrations, cesium coverage of a target is proportional to the ratio of (1 - β)/γ where β is the reflection coefficient and γ is the sputter yield. High coverages are produced on molybdenum due to implantation and low backscattering, because molybdenum is lighter than cesium. For tungsten the high backscattering and low implantation result in low coverages

  19. Ion exchange separation of nitrate from uranium compounds and its determination by spectrophotometry and ion chromatography

    International Nuclear Information System (INIS)

    Pires, M.A.F.; Atalla, L.T.; Abrao, A.

    1985-11-01

    A procedure for the separation of nitrate from uranium compounds by retaintion of uranyl ion on a cationic ion exchanger and its determination in the effluent is described. Nitrate is analysed by the spectrometric method with 1-phenol-2,4-dissulphonic acid. This determination covers the 1 to 10 μg NO - 3 /mL range and requires an amount of 10 to 100 μg NO - 3 . The main interference is uranium (VI) due its own intense yellow color. This difficulty is overcome by the complete separation of UO 2 ++ with the cationic resin. Alternatively, the ion chromatography technique is used for the determination of nitrate in the effluent of the cationic resin. The determination was easily made by the comparison of the nitrate peak hights of the analyte and the standard solutions. The ion chromatography method is very sensitive (0,3 μg NO - 3 /mL), reproducible and suitable for routine analysis and permits the determination of fraction of part per million of nitrate in uranium. The results of nitrate determination using both spectrophotometric and ion chromatography techniques are compared. The method is being routinely applied for the quality control of uranium compounds in the fuel cycle, specially uranium oxide, ammonium diuranate, uranium peroxide and ammonium uranyl tricarbonate. (Author) [pt

  20. Coprecipitation of alkali metal ions with calcium carbonate

    International Nuclear Information System (INIS)

    Okumura, Minoru; Kitano, Yasushi

    1986-01-01

    The coprecipitation of alkali metal ions Li + , Na + , K + and Rb + with calcium carbonate has been studied experimentally and the following results have been obtained: (1) Alkali metal ions are more easily coprecipitated with aragonite than with calcite. (2) The relationship between the amounts of alkali metal ions coprecipitated with aragonite and their ionic radii shows a parabolic curve with a peak located at Na + which has approximately the same ionic radius as Ca 2+ . (3) However, the amounts of alkali metal ions coprecipitated with calcite decrease with increasing ionic radius of alkali metals. (4) Our results support the hypothesis that (a) alkali metals are in interstitial positions in the crystal structure of calcite and do not substitute for Ca 2+ in the lattice, but (b) in aragonite, alkali metals substitute for Ca 2+ in the crystal structure. (5) Magnesium ions in the parent solution increase the amounts of alkali metal ions (Li + , Na + , K + and Rb + ) coprecipitated with calcite but decrease those with aragonite. (6) Sodium-bearing aragonite decreases the incorporation of other alkali metal ions (Li + , K + and Rb + ) into the aragonite. (author)

  1. Which metal or ion? Identification of metals and ions in protein structures

    Czech Academy of Sciences Publication Activity Database

    Dohnálek, Jan

    2014-01-01

    Roč. 70, Supplement /August/ (2014), C1484 ISSN 0108-7673. [Congress and General Assembly of the International Union of Crystallography /23./ - IUCr 2014. 05.08.2014-12.08.2014, Montreal] R&D Projects: GA MŠk(CZ) EE2.3.30.0029; GA MŠk(CZ) ED1.1.00/02.0109 Institutional support: RVO:61389013 Keywords : metal s * ions * structure validation Subject RIV: CE - Biochemistry

  2. Characterization of Metal Ion ­ Colloid Interaction: Impact On Colloid-facilitated Transport

    Science.gov (United States)

    Specht, C. H.; Schmitt, D.; Kaulisch, E.-M.; Frimmel, F. H.

    It is generally accepted, that metal transport in natural aquatic systems strongly de- pends on the metal binding form. Besides complex formation with well defined inor- ganic and organic ligands, the interaction with colloidal particles and soil material is one of the most important reactions of metal ions in aquatic systems. Mobile colloids compete with the stationary soil matrix for binding of metal ions and might facili- tate their transport. Important representatives for mineral and organic colloids are clay minerals and natural organic matter (NOM), respectively. In this work, the interaction of metal ions with clay minerals and NOM is characterized by coupling of asymmetric flow field-flow fractionation AF4 to inductively coupled plasma ­ mass spectrometry (ICPMS). A method for separating mineral from organic colloids is presented, which allows to quantify the amount of metals being bound to either colloid. For different metal ions (Cu, Zn, Pb, Pt) and a metalloid (As) a different extent of binding to either colloid was found.The information obtained from the AF4-ICPMS measurements was useful for the understanding of the observations from column experiments which were conducted to quantify the colloid-facilitated metal transport. In column experiments, the transport of the mineral colloids itself and the influence of NOM onto the colloid transport were investigated. Furthermore, the dependance of colloid transport from the ionic strength and the pH value was elucidated. In order to get information about the co-transport of metal ions by organic and mineral colloids, metal ions were adsorbed onto the colloidal material and a distribution coef- ficient of the metal ions between the colloidal phase and the solution was determined. The colloidal suspension containing both, "free" and adsorbed metal ions were then injected onto the column. The direct metal breakthrough caused by colloidal trans- port was detected at the column outlet. The results clearly

  3. Metal ion transport in eukaryotic microorganisms: insights from Saccharomyces cerevisiae.

    Science.gov (United States)

    Eide, D J

    2000-01-01

    Metal ions such as iron, copper, manganese, and zinc are essential nutrients for all eukaryotic microorganisms. Therefore, these organisms possess efficient uptake mechanisms to obtain these nutrients from their extracellular environment. Metal ions must also be transported into intracellular organelles where they function as catalytic and structural cofactors for compartmentalized enzymes. Thus, intracellular transport mechanisms are also present. When present in high levels, metal ions can also be toxic, so their uptake and intracellular transport is tightly regulated at both transcriptional and post-transcriptional levels to limit metal ion overaccumulation and facilitate storage and sequestration. Remarkable molecular insight into these processes has come from recent studies of the yeast Saccharomyces cerevisiae. This organism, which is the primary subject of this chapter, serves as a useful paradigm to understand metal ion metabolism in other eukaryotic microbes.

  4. Multiheteromacrocycles that Complex Metal Ions. Ninth Progress Report (includes results of last three years), 1 May 1980 -- 30 April 1983

    Science.gov (United States)

    Cram, D. J.

    1982-09-15

    The overall objective of this research is to design, synthesize, and evaluate cyclic and polycyclic host organic compounds for the abilities to complex and lipophilize guest metal ions, their complexes, and their clusters. Host organic compounds consist of strategically placed solvating, coordinating, and ion-pairing sites tied together by covalent bonds through hydrocarbon units around cavities shaped to be occupied by guest metal ions, or by metal ions plus their ligands. Specificity in complexation is sought by matching the following properties of host and guest: cavity and metal ion sizes; geometric arrangements of binding sites; numbers of binding sites; characters of binding sites; and valences. The hope is to synthesize new classes of compounds useful in the separation of metal ions, their complexes, and their clusters.

  5. Electrodialytic treatment of sewage sludge ash for the recovery of phosphorous and separation of heavy metals

    DEFF Research Database (Denmark)

    Ebbers, Benjamin; Ottosen, Lisbeth M.; Jensen, Pernille Erland

    2012-01-01

    Mobilization and extraction of both phosphorus (P) and heavy metals (HM) from sewage sludge ash through means of acidification has been studied extensively. However, separation of both P and HM after mobilization to provide reusable materials has proven to be challenging. This study presents...... a combination of acidification and electrodialytic separation (EDS) to mobilize and separate P and HM from sewage sludge ash (SSA). The EDS experimental setup consists of three compartments, separated by ion exchange membranes which are located at either side of the stirred ash suspension. Through application...... of a direct current to electrodes in the outer compartments, ionic complexes migrate and concentrate in the electrode compartments in accordance to their charge. Application of both EDS and acidification of the ash resulted in an increased release of phosphorus from the ash, but did not always result...

  6. Ultraefficient separation and sensing of mercury and methylmercury ions in drinking water by using aminonaphthalimide-functionalized Fe(3)O(4)@SiO(2) core/shell magnetic nanoparticles.

    Science.gov (United States)

    Park, Minsung; Seo, Sungmin; Lee, In Su; Jung, Jong Hwa

    2010-07-07

    A new fluorogenic based aminonaphthalimide-functionalized Fe(3)O(4)@SiO(2) core/shell magnetic nanoparticles 1 has been prepared, and its abilities to sense and separate metal ions were evaluated by fluorophotometry. The nanoparticles 1 exhibited a high affinity and selectivity for Hg(2+) and CH(3)Hg(+) ions over competing metal ions.

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

    Energy Technology Data Exchange (ETDEWEB)

    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

  8. DNA as sensors and imaging agents for metal ions.

    Science.gov (United States)

    Xiang, Yu; Lu, Yi

    2014-02-17

    Increasing interest in detecting metal ions in many chemical and biomedical fields has created demands for developing sensors and imaging agents for metal ions with high sensitivity and selectivity. This review covers recent progress in DNA-based sensors and imaging agents for metal ions. Through both combinatorial selection and rational design, a number of metal-ion-dependent DNAzymes and metal-ion-binding DNA structures that can selectively recognize specific metal ions have been obtained. By attachment of these DNA molecules with signal reporters such as fluorophores, chromophores, electrochemical tags, and Raman tags, a number of DNA-based sensors for both diamagnetic and paramagnetic metal ions have been developed for fluorescent, colorimetric, electrochemical, and surface Raman detection. These sensors are highly sensitive (with a detection limit down to 11 ppt) and selective (with selectivity up to millions-fold) toward specific metal ions. In addition, through further development to simplify the operation, such as the use of "dipstick tests", portable fluorometers, computer-readable disks, and widely available glucose meters, these sensors have been applied for on-site and real-time environmental monitoring and point-of-care medical diagnostics. The use of these sensors for in situ cellular imaging has also been reported. The generality of the combinatorial selection to obtain DNAzymes for almost any metal ion in any oxidation state and the ease of modification of the DNA with different signal reporters make DNA an emerging and promising class of molecules for metal-ion sensing and imaging in many fields of applications.

  9. Selective separation of radionuclides from nuclear waste solutions with inorganic ion exchangers

    International Nuclear Information System (INIS)

    Lehto, J.; Harjula, R.

    1999-01-01

    Nuclear industry produces and stores large volumes of radioactive waste solutions. Removal of radionuclides from the solutions is an important and challenging task for two main reasons: reductions in the volumes of solidified waste, which have to be disposed of, and reductions in the radioactive discharges into the environment. Since the radioactive elements in most waste solutions are in trace concentrations and the waste solutions contain large excesses of inactive metal ions, highly selective separation methods are needed for the removal of radionuclides. A number of inorganic ion exchange materials are very selective to key radionuclides and they can play an important role in solving these problems. The spectrum of nuclear waste solutions is rather wide considering their radionuclide contents, concentrations of interfering salts and acidity/alkalinity. Therefore, several inorganic ions exchangers are needed for the removal of most harmful radionuclides from a variety of solutions. This paper discusses the use and requirements of inorganic ion exchange materials in nuclear waste management. Special attention is paid to the novel ion exchange materials developed in the Laboratory of Radiochemistry, University of Helsinki. (orig.)

  10. Metal ion binding with dehydroannulenes – Plausible two ...

    Indian Academy of Sciences (India)

    WINTEC

    has highest interaction energy of –50∙6 kcal/mol at. B3LYP/6-311++G** level and is 128∙0 kcal/mol more than 1′-K+ complex. Understandably, the binding energy of metal complexes decreases with increase in the size of the metal ion, in accordance with ear- lier results.16,21. Placement of the metal ions at the centroid of ...

  11. Shape Separation of Colloidal Metal Nanoparticles via Size Exclusion Chromatography

    OpenAIRE

    Marvi, Sarrah

    2016-01-01

    The inherent polydispersity of solution-based, colloidal nanoparticle syntheses has necessitated the development of facile post-processing methods for the purification of anisotropic nanoparticles. Here, the use of size exclusion chromatography is explored for the shape separation of colloidal silver nanocube and colloidal gold bipyramid solutions. Multiple column packing materials, pore sizes, and mobile phases were tested to address the prevalent issues of metal adsorption to the high surfa...

  12. Controlled Fabrication of Metallic Electrodes with Atomic Separation

    DEFF Research Database (Denmark)

    Morpurgo, A.; Robinson, D.; M. Marcus, C.

    1998-01-01

    We report a new technique for fabricating metallic electrodes on insulating substrates with separations on the 1 nm scale. The fabrication technique, which combines lithographic and electrochemical methods, provides atomic resolution without requiring sophisticated instrumentation. The process...... is simple, controllable, reversible, and robust, allowing rapid fabrication of electrode pairs with high yield. We expect the method to prove useful in interfacing molecular-scale structures to macroscopic probes and electronic devices ....

  13. Alkali metal ion battery with bimetallic electrode

    Science.gov (United States)

    Boysen, Dane A; Bradwell, David J; Jiang, Kai; Kim, Hojong; Ortiz, Luis A; Sadoway, Donald R; Tomaszowska, Alina A; Wei, Weifeng; Wang, Kangli

    2015-04-07

    Electrochemical cells having molten electrodes having an alkali metal provide receipt and delivery of power by transporting atoms of the alkali metal between electrode environments of disparate chemical potentials through an electrochemical pathway comprising a salt of the alkali metal. The chemical potential of the alkali metal is decreased when combined with one or more non-alkali metals, thus producing a voltage between an electrode comprising the molten the alkali metal and the electrode comprising the combined alkali/non-alkali metals.

  14. Separation of platinum metals by theirs extraction as sulfides

    International Nuclear Information System (INIS)

    Pilipenko, A.T.; Ryabushko, O.P.; Ty Van Mak

    1978-01-01

    Separation of platinum metals by means of their sediment in the form of sulfides with subsequent extraction is studied. The optimum conditions of metal sulfide extraction are determined, the metal output dependence from acidness and aqueous phase composition and also the organic solvent nature are investigated. Ruthenium concentration was determined photometrically. Ruthenium sulfide is extracted by butyl spirit from 1-4 normal hydrochloric acid. The maximum extraction grade of 63% is reached in 3.2-normal acid. When the mixture of acetic and hydrochloric acids (2:1) is used for decomposition of ruthenium tiosalts, the grade of ruthenium extraction by amyl spirit or the mixture of anyl and butyl spirits (1:1) constitutes 100%

  15. Influence of the inert and active ion bombardment on structure of the transition metal thin films

    CERN Document Server

    Blazhevich, S; Martynov, I; Neklyudov, I

    2002-01-01

    The results of the experimental research of the inert (He, Ne, Ar, Kr, Xe) and active (O, N) ion impact on the transition metal structure are presented. Thin high-purity (99.999 at.%) films of nickel, chrome and iron were used in the experiment. The bombardment was realized under room temperature at high vacuum (P<1x10 sup - sup 7 Pa) by a separated ion beam of 10-10 sup 3 keV. As a main result of the experiment, the full absence of crystal matrix changes was ascertained for all the transition metals irradiated by inert gas ions. The chemical nature of the crystal structure changes observed in transition metals being under active ion bombardment was found out too.

  16. Hydrometallurgical recovery of metal values by the use of ion exchange

    International Nuclear Information System (INIS)

    Higgins, I.R.

    1982-01-01

    This paper presented what had been accomplished to date using Packed Bed Continuous Countercurrent Ion Exchange (CCIX) and proposed plans for more comprehensive systems that include many soluble metals of value. Frontiers of hydrometallurgy cannot be breached until advantage is taken of a multitude of metal ions in solution. The future utilization of hydrometallurgical methodology depends on the success of extraction and separation unit operations and being accepted by mining companies. Examples are presented of CCIX projects in operation and pilot plants tested as proof of the special attractive features of the Chem-Seps CCIX system. An overall plan was presented for processing of sulfide type mineralization, with emphasis on making an effort to get ''complete'' dissolution of all metals of value. Continuous Countercurrent Ion Exchange plays a vital role in hydrometallurical processing because of the need to handle prodigious volumes of solution, tremendous tonnages of salts, and to compensate for poor ion exchange equilibrium. 11 figures. (DP)

  17. Sorption of Molecular Oxygen by Metal-Ion Exchanger Nanocomposites

    Science.gov (United States)

    Krysanov, V. A.; Plotnikova, N. V.; Kravchenko, T. A.

    2018-03-01

    Kinetic features are studied of the chemisorption and reduction of molecular oxygen from water by metal-ion exchanger nanocomposites that differ in the nature of the dispersed metal and state of oxidation. In the Pd equilibrium sorption coefficient for oxygen dissolved in water ranges from 20 to 50, depending on the nature and oxidation state of the metal component.

  18. Initiation of protein association in tofu formation by metal ions.

    Science.gov (United States)

    Arii, Yasuhiro; Takenaka, Yasuyuki

    2014-01-01

    Magnesium and calcium ions are important factors in making tofu. However, the molecular role of these ions remains unclear in tofu formation. We have previously shown that magnesium chloride concentration-dependent produced silken tofu-like (SP) and regular tofu-like (RP) precipitates, but was an inconsequential factor for the retention of tofu. We investigated in this present study, the effect of various metal chlorides on the metal chloride concentration-dependent changes in tofu formation. These changes occurred in a similar manner to that of the magnesium ion, in which SP formation was followed by RP formation. It is interesting that the midpoint concentration for the formation of SP and RP represented a good correlation with the stability constant of EDTA. This correlation demonstrated the possibility that metal ions would interact with the carboxyl groups of soy proteins. We consider from these results that metal ions were the initiators of protein association in tofu formation.

  19. Catalysis using hydrous metal oxide ion exchanges

    Science.gov (United States)

    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.

  20. Metallic ion release from biocompatible cobalt-based alloy

    Directory of Open Access Journals (Sweden)

    Dimić Ivana D.

    2014-01-01

    Full Text Available Metallic biomaterials, which are mainly used for the damaged hard tissue replacements, are materials with high strength, excellent toughness and good wear resistance. The disadvantages of metals as implant materials are their susceptibility to corrosion, the elastic modulus mismatch between metals and human hard tissues, relatively high density and metallic ion release which can cause serious health problems. The aim of this study was to examine metallic ion release from Co-Cr-Mo alloy in artificial saliva. In that purpose, alloy samples were immersed into artificial saliva with different pH values (4.0, 5.5 and 7.5. After a certain immersion period (1, 3 and 6 weeks the concentrations of released ions were determined using Inductively Coupled Plasma - Mass Spectrophotometer (ICP-MS. The research findings were used in order to define the dependence between the concentration of released metallic ions, artificial saliva pH values and immersion time. The determined released metallic ions concentrations were compared with literature data in order to describe and better understand the phenomenon of metallic ion release from the biocompatible cobalt-based alloy. [Projekat Ministarstva nauke Republike Srbije, br. III 46010 i br. ON 174004

  1. Status report of the Jyvaskyla ion guide isotope separator on-line facility

    NARCIS (Netherlands)

    Penttila, H; Dendooven, P; Honkanen, A; Huhta, M; Jauho, PP; Jokinen, A; Lhersonneau, G; Oinonen, M; Parmonen, JM; Perajarvi, K; Aysto, J

    The ion guide isotope separator facility IGISOL of the University of Jyvaskyla has been moved to the new K-130 heavy ion cyclotron laboratory. The totally reconstructed facility is described in detail. The primary beams and targets, helium pumping, separator beam line construction and separator beam

  2. An Animal Model Using Metallic Ions to Produce Autoimmune Nephritis

    Directory of Open Access Journals (Sweden)

    Roxana Ramírez-Sandoval

    2015-01-01

    Full Text Available Autoimmune nephritis triggered by metallic ions was assessed in a Long-Evans rat model. The parameters evaluated included antinuclear autoantibody production, kidney damage mediated by immune complexes detected by immunofluorescence, and renal function tested by retention of nitrogen waste products and proteinuria. To accomplish our goal, the animals were treated with the following ionic metals: HgCl2, CuSO4, AgNO3, and Pb(NO32. A group without ionic metals was used as the control. The results of the present investigation demonstrated that metallic ions triggered antinuclear antibody production in 60% of animals, some of them with anti-DNA specificity. Furthermore, all animals treated with heavy metals developed toxic glomerulonephritis with immune complex deposition along the mesangium and membranes. These phenomena were accompanied by proteinuria and increased concentrations of urea. Based on these results, we conclude that metallic ions may induce experimental autoimmune nephritis.

  3. Heavy metal ions are potent inhibitors of protein folding.

    Science.gov (United States)

    Sharma, Sandeep K; Goloubinoff, Pierre; Christen, Philipp

    2008-07-25

    Environmental and occupational exposure to heavy metals such as cadmium, mercury and lead results in severe health hazards including prenatal and developmental defects. The deleterious effects of heavy metal ions have hitherto been attributed to their interactions with specific, particularly susceptible native proteins. Here, we report an as yet undescribed mode of heavy metal toxicity. Cd2+, Hg2+ and Pb2+ proved to inhibit very efficiently the spontaneous refolding of chemically denatured proteins by forming high-affinity multidentate complexes with thiol and other functional groups (IC(50) in the nanomolar range). With similar efficacy, the heavy metal ions inhibited the chaperone-assisted refolding of chemically denatured and heat-denatured proteins. Thus, the toxic effects of heavy metal ions may result as well from their interaction with the more readily accessible functional groups of proteins in nascent and other non-native form. The toxic scope of heavy metals seems to be substantially larger than assumed so far.

  4. Synthesis and Characterization of Quaternary Metal Chalcogenide Aerogels for Gas Separation and Volatile Hydrocarbon Adsorption

    KAUST Repository

    Edhaim, Fatimah A.

    2017-11-01

    In this dissertation, the metathesis route of metal chalcogenide aerogel synthesis was expanded by conducting systematic studies between polysulfide building blocks and the 1st-row transition metal linkers. Resulting materials were screened as sorbents for selective gas separation and volatile organic compounds adsorption. They showed preferential adsorption of polarizable gases (CO2) and organic compounds (toluene). Ion exchange and heavy metal remediation properties have also been demonstrated. The effect of the presence of different counter-ion within chalcogel frameworks on the adsorption capacity of the chalcogels was studied on AFe3Zn3S17 (A= K, Na, and Rb) chalcogels. The highest adsorption capacity toward hydrocarbons and gases was observed on Rb based chalcogels. Adopting a new building block [BiTe3]3- with the 1st-row transition metal ions results in the formation of three high BET surface area chalcogels, KCrBiTe3, KZnBiTe3, and KFeBiTe3. The resulting chalcogels showed preferential adsorption of toluene vapor, and remarkable selectivity of CO2, indicating the potential future use of chalcogels in adsorption-based gas or hydrocarbon separation processes. The synthesis and characterization of the rare earth chalcogels NaYSnS4, NaGdSnS4, and NaTbSnS4 are also reported. Rare earth metal ions react with the thiostannate clusters in formamide solution forming extended polymeric networks by gelation. Obtained chalcogels have high BET surface areas, and showed notable adsorption capacity toward CO2 and toluene vapor. These chalcogels have also been engaged in the absorption of different organic molecules. The results reveal the ability of the chalcogels to distinguish among organic molecules on their electronic structures; hence, they could be used as sensors. Furthermore, the synthesis of metal chalcogenide aerogels Co0.5Sb0.33MoS4 and Co0.5Y0.33MoS4 by the sol-gel method is reported. In this system, the building blocks [MoS4]2- chelated with Co2+ and (Sb3

  5. Highly dispersive ion exchangers in the analytical chemistry of uranium, particularly regarding separation methods

    International Nuclear Information System (INIS)

    Schoening, R.

    1975-01-01

    The reaction of water-insoluble polyvinyl pyrrolidon with uranium VI was investigated and a determination method for uranium was worked out in which the polyvinyl pyrrolidon was used as specific exchanger. Good separations of uranium from numerous transition metal ions were achieved here. The application of this exchanger for a fast and simple elution and determination method was of particular importance. A possible sorption mechanism was suggested based on the capacity curve of uranium with polyvinyl pyrrolidon and nitrogen and chloride content at maximum load. The sorption occurs by coordination of the carbonyl oxygen of single pyrrolidon rings with the protons of the complex acides and uranium. This assumption is supported by IR investigations. The sorbability of other inorganic acids was also investigated and possible structures were formulated for the sorption mechanism. In addition to this, ion exchangers were prepared based on cellulose by converting cellulose powder with aziridine and tris-1-aziridinyl-phosphine oxide. A polyethylene imine cellulose of high capacity was obtained in the conversion of cellulose powder with aziridine. This exchanger absorbs cobalt III very strongly. The exchanger loaded with cobalt III was used to separate the uranium as cyanato complex. The exchanger obtained in converting chlorated cellulose with tris-1-aziridinyl phosphine oxide also absorbs uranium VI very strongly. Thus a separation method of high specifity and selectivity was developed. (orig.) [de

  6. Air separation of heavy metal contaminants from soil

    International Nuclear Information System (INIS)

    Nelson, M.E.; Harper, M.J.; Buckon, A.D.

    1995-01-01

    Several heavy metal separation techniques are currently being developed for soil remediation at various Department of Defense and Department of Energy (DOE) Facilities. The majority of these techniques involve a wet process using water, pH modifiers or other compounds. The US Naval Academy (USNA) has developed a dry process for heavy metal separation. The process uses air classification technology to concentrate the metal contaminant into a fraction of the soil. The advantages of this dry process are that it creates no contaminated byproduct and uses commercially available technology. The USNA process is based on using a Gayco-Reliance air classifier. Tests have been conducted with the system at the Naval Academy and the University of Nevada-Reno (UNR). The USNA tests used soil from the Nevada Test Site mixed with bismuth at a concentration of 500--1,000 ppm. The UNR tests used soil from four DOE sites mixed with uranium oxides and plutonium at an activity level of 100--700 pCi per gram. Concentration of activities and volume reduction percentages are presented for the various soils and contaminants tested

  7. Ion optical system of a 255 deg double-focusing electromagnetic isotope separator at IAE

    International Nuclear Information System (INIS)

    Mao Naifeng; Lu Hongyou; Cai Rentai

    1987-01-01

    The ion optical system of a 255 deg double-focusing electro-magnetic isotope separator at the Institute of Atomic Energy (IAE), Beijing, is described, including the analysis of ion beam focusing and the calculation of magnetic field shaping

  8. Metal ion removal from aqueous solution using physic seed hull.

    Science.gov (United States)

    Mohammad, Masita; Maitra, Saikat; Ahmad, Naveed; Bustam, Azmi; Sen, T K; Dutta, Binay K

    2010-07-15

    The potential of physic seed hull (PSH), Jantropha curcas L. as an adsorbent for the removal of Cd(2+) and Zn(2+) metal ions from aqueous solution has been investigated. It has been found that the amount of adsorption for both Cd(2+) and Zn(2+) increased with the increase in initial metal ions concentration, contact time, temperature, adsorbent dosage and the solution pH (in acidic range), but decreased with the increase in the particle size of the adsorbent. The adsorption process for both metal ions on PSH consists of three stages-a rapid initial adsorption followed by a period of slower uptake of metal ions and virtually no uptake at the final stage. The kinetics of metal ions adsorption on PSH followed a pseudo-second-order model. The adsorption equilibrium data were fitted in the three adsorption isotherms-Freundlich, Langmuir and Dubinin-Radushkevich isotherms. The data best fit in the Langmuir isotherm indication monolayer chemisorption of the metal ions. The adsorption capacity of PSH for both Zn(2+) and Cd(2+) was found to be comparable with other available adsorbents. About 36-47% of the adsorbed metal could be leached out of the loaded PSH using 0.1M HCl as the eluting medium. 2010 Elsevier B.V. All rights reserved.

  9. Catalytic metal ions and enzymatic processing of DNA and RNA.

    Science.gov (United States)

    Palermo, Giulia; Cavalli, Andrea; Klein, Michael L; Alfonso-Prieto, Mercedes; Dal Peraro, Matteo; De Vivo, Marco

    2015-02-17

    CONSPECTUS: Two-metal-ion-dependent nucleases cleave the phosphodiester bonds of nucleic acids via the two-metal-ion (2M) mechanism. Several high-resolution X-ray structures portraying the two-metal-aided catalytic site, together with mutagenesis and kinetics studies, have demonstrated a functional role of the ions for catalysis in numerous metallonucleases. Overall, the experimental data confirm the general mechanistic hypothesis for 2M-aided phosphoryl transfer originally reported by Steitz and Steitz ( Proc. Natl. Acad. Sci. U.S.A. 1993 , 90 ( 14 ), 6498 - 6502 ). This seminal paper proposed that one metal ion favors the formation of the nucleophile, while the nearby second metal ion facilitates leaving group departure during RNA hydrolysis. Both metals were suggested to stabilize the enzymatic transition state. Nevertheless, static X-ray structures alone cannot exhaustively unravel how the two ions execute their functional role along the enzymatic reaction during processing of DNA or RNA strands when moving from reactants to products, passing through metastable intermediates and high-energy transition states. In this Account, we discuss the role of multiscale molecular simulations in further disclosing mechanistic insights of 2M-aided catalysis for two prototypical enzymatic targets for drug discovery, namely, ribonuclease H (RNase H) and type II topoisomerase (topoII). In both examples, first-principles molecular simulations, integrated with structural data, emphasize a cooperative motion of the bimetal motif during catalysis. The coordinated motion of both ions is crucial for maintaining a flexible metal-centered structural architecture exquisitely tailored to accommodate the DNA or RNA sugar-phosphate backbone during phosphodiester bond cleavage. Furthermore, our analysis of RNase H and the N-terminal domain (PAN) of influenza polymerase shows that classical molecular dynamics simulations coupled with enhanced sampling techniques have contributed to describe

  10. Designer ligands: The search for metal ion selectivity

    Directory of Open Access Journals (Sweden)

    Perry T. Kaye

    2011-03-01

    Full Text Available The paper reviews research conducted at Rhodes University towards the development of metal-selective ligands. The research has focused on the rational design, synthesis and evaluation of novel ligands for use in the formation of copper complexes as biomimetic models of the metalloenzyme, tyrosinase, and for the selective extraction of silver, nickel and platinum group metal ions in the presence of contaminating metal ions. Attention has also been given to the development of efficient, metal-selective molecular imprinted polymers.

  11. Surface enhanced Raman spectroscopy as a new spectral technique for quantitative detection of metal ions.

    Science.gov (United States)

    Temiz, Havva Tumay; Boyaci, Ismail Hakki; Grabchev, Ivo; Tamer, Ugur

    2013-12-01

    Four newly synthesized poly (propylene amine) dendrimers from first and second generation modified with 1,8-naphthalimide units in the dendrimer periphery have been investigated as ligands for the detection of heavy metal ions (Al(3+), Sb(2+), As(2+), Cd(2+) and Pb(2+)) by surface-enhanced Raman spectroscopy. Calibration curves were established for all metal ions between the concentration ranges of 1 x 10(-6) to 5 x 10(-4) M. It has been shown that these dendrimers can be coordinated, especially with different metal ions. Using dendrimer molecules and silver colloids at the same time allowed us to obtain an SERS signal from the abovementioned metal ions at very low concentrations. Principle component analysis (PCA) analysis was also applied to the collected SERS data. Four different PCA models were developed to accomplish the discrimination of five metal ions, which interacted with each of the four dendrimer molecules, separately. A detailed investigation was performed in the present study to provide the basis of a new approach for heavy metal detection. Copyright © 2013 Elsevier B.V. All rights reserved.

  12. Studies on regularities of metal ion sorption from seawater by clinoptilolytes of different origin

    International Nuclear Information System (INIS)

    Khamizov, R.Kh.; Butenko, T.Yu.; Bronov, L.V.; Skovyra, V.V.; Novikova, V.A.; AN SSSR, Vladivostok

    1988-01-01

    The regularities of metal ion sorption from sea water by different clinoptilolyte (CP) samples are studied with the purpose of choosing the most prospective sorbents to extract strontium and rubidium. It is shown that the internal diffusion is the sorption rate determining stage. The dependence of effective coefficients of internal diffusion on the exchange level is determined. The distribution coefficients and those of single metal ion separation are determined, the series of sorption selectivity are determined. All CP studied can be used for initial Rb concentration from sea water, and to extract strontium it is advisable to use zeolites of Dzegvi and Tedzami deposits

  13. The fabrication and modification of capillary polymer monoliths for the separation of small ions

    OpenAIRE

    Moyna, Aine

    2012-01-01

    The fabrication and modification of polymer monoliths, in capillary formats, for the separation of small ions is presented. The separation of small ions using polymer monoliths has limitations and this work aims to investigate increasing the ion exchange capacity using photo-grafting techniques. Chapter 1.0 includes a comprehensive review on the use of capillary ion chromatography including advancements made in capillary instrumentation, stationary phases and detection devices. This chapter a...

  14. Study on rare earths complexes separation by means of different type of ion exchangers

    International Nuclear Information System (INIS)

    Hubicka, H.

    1990-01-01

    The applicability of different types of ion exchangers for purification and separation of rare earths complexes has been examined. The experimental work has been carried out on 14 chelating ion exchangers. The investigation results proved the great usefulness chelating ion exchangers especially of amino acid and phosphorus-type. Application of that type ion exchangers in column chromatographic process gave the excellent rare earths separation as well as enabled to obtain their preparates of high purity. 218 refs, 21 figs, 27 tabs

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

    Energy Technology Data Exchange (ETDEWEB)

    Peters, R.W.; Shem, L.

    1993-03-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Peters, R.W.; Shem, L.

    1993-01-01

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

  17. Complexation-Induced Phase Separation: Preparation of Metal-Rich Polymeric Membranes

    KAUST Repository

    Villalobos Vazquez de la Parra, Luis Francisco

    2017-08-01

    The majority of state-of-the-art polymeric membranes for industrial or medical applications are fabricated by phase inversion. Complexation induced phase separation (CIPS)—a surprising variation of this well-known process—allows direct fabrication of hybrid membranes in existing facilities. In the CIPS process, a first step forms the thin metal-rich selective layer of the membrane, and a succeeding step the porous support. Precipitation of the selective layer takes place in the same solvent used to dissolve the polymer and is induced by a small concentration of metal ions. These ions form metal-coordination-based crosslinks leading to the formation of a solid skin floating on top of the liquid polymer film. A subsequent precipitation in a nonsolvent bath leads to the formation of the porous support structure. Forming the dense layer and porous support by different mechanisms while maintaining the simplicity of a phase inversion process, results in unprecedented control over the final structure of the membrane. The thickness and morphology of the dense layer as well as the porosity of the support can be controlled over a wide range by manipulating simple process parameters. CIPS facilitates control over (i) the thickness of the dense layer throughout several orders of magnitude—from less than 15 nm to more than 6 μm, (ii) the type and amount of metal ions loaded in the dense layer, (iii) the morphology of the membrane surface, and (iv) the porosity and structure of the support. The nature of the CIPS process facilitates a precise loading of a high concentration of metal ions that are located in only the top layer of the membrane. Moreover, these metal ions can be converted—during the membrane fabrication process—to nanoparticles or crystals. This simple method opens up fascinating possibilities for the fabrication of metal-rich polymeric membranes with a new set of properties. This dissertation describes the process in depth and explores promising

  18. Determination of Heavy Metal Ions in Tobacco and Tobacco Additives

    African Journals Online (AJOL)

    NJD

    aminophenyl)-porphyrin, heavy metal ions. 1. Introduction ..... Application. This method was applied to the determination of Co, Ni, Sn,. Hg, Pb and Cd in the glycerol, tobacco leaf, tobacco sauce and cigarette samples. The samples were prepared ...

  19. Adhesive, abrasive and oxidative wear in ion-implanted metals

    International Nuclear Information System (INIS)

    Dearnaley, G.

    1985-01-01

    Ion implantation is increasingly being used to provide wear resistance in metals and cemented tungsten carbides. Field trials and laboratory tests indicate that the best performance is achieved in mild abrasive wear. This can be understood in terms of the classification of wear modes (adhesive, abrasive, oxidative etc.) introduced by Burwell. Surface hardening and work hardenability are the major properties to be enhanced by ion implantation. The implantation of nitrogen or dual implants of metallic and interstitial species are effective. Recently developed techniques of ion-beam-enhanced deposition of coatings can further improve wear resistance by lessening adhesion and oxidation. In order to support such hard coatings, ion implantation of nitrogen can be used as a preliminary treatment. There is thus emerging a versatile group of related hard vacuum treatments involving intense beams of nitrogen ions for the purpose of tailoring metal surfaces to resist wear. (Auth.)

  20. Metal Ion Selectivity of Kojate Complexes: A Theoretical Study

    Directory of Open Access Journals (Sweden)

    Sarita Singh

    2013-01-01

    Full Text Available Density functional calculations have been performed on four-coordinate kojate complexes of selected divalent metal ions in order to determine the affinity of the metal ions for the kojate ion. The complexation reactions are characterized by high energies, showing that they are highly exothermic. It is found that Ni(II exhibits the highest affinity for the kojate ion, and this is attributed to the largest amount of charge transfer from the ligand to the metal ion. The Ni(II complex has distorted square planar structure. The HOMOs and LUMOs of the complexes are also discussed. All complexes display a strong band at ~1500 cm−1 corresponding to the stretching frequency of the weakened carbonyl bond. Comparison of the complexation energies for the two steps shows that most of the complexation energy is realized in the first step. The energy released in the second step is about one-third that of the first step.

  1. A versatile MOF-based trap for heavy metal ion capture and dispersion

    OpenAIRE

    Peng, Yaguang; Huang, Hongliang; Zhang, Yuxi; Kang, Chufan; Chen, Shuangming; Song, Li; Liu, Dahuan; Zhong, Chongli

    2018-01-01

    Current technologies for removing heavy metal ions are typically metal ion specific. Herein we report the development of a broad-spectrum heavy metal ion trap by incorporation of ethylenediaminetetraacetic acid into a robust metal-organic framework. The capture experiments for a total of 22 heavy metal ions, covering hard, soft, and borderline Lewis metal ions, show that the trap is very effective, with removal efficiencies of >99% for single-component adsorption, multi-component adsorption, ...

  2. Liquid metal field-emission ion sources and their applications

    International Nuclear Information System (INIS)

    Prewett, P.D.; Jefferies, D.K.

    1980-01-01

    The study of ion emission from liquid metal surfaces under the action of high electric fields has led to the development of ion sources of exceptionally high brightness. The design and operating characteristics of commercially manufactured sources of gallium and gold ions are described. Preliminary focusing and scanning experiments have produced spots estimated to be approximately 0.5 μm diameter at currents approximately 0.2 nA using an electrostatic ion optical system. A focused Ga + beam has been used as an ion microprobe for imaging and for elemental mapping of surfaces by SIMS. (author)

  3. [Detection of metal ions in hair after metal-metal hip arthroplasty].

    Science.gov (United States)

    Hernandez-Vaquero, D; Rodríguez de la Flor, M; Fernandez-Carreira, J M; Sariego-Muñiz, C

    2014-01-01

    There is an increase in the levels of metals in the serum and urine after the implantation of some models of metal-metal hip prosthesis. It has recently been demonstrated that there is an association between these levels and the levels found in hair. The aim of this study is to determine the presence of metals in hair, and to find out whether these change over time or with the removal of the implant. The levels of chromium, cobalt and molybdenum were determined in the hair of 45 patients at 3, 4, 5, and 6 years after a hip surface replacement. The mean age was 57.5 years, and two were female. Further surgery was required to remove the replacement and implant a new model with metal-polyethylene friction in 11 patients, 5 of them due to metallosis and a periarticular cyst. The mean levels of metals in hair were chromium 163.27 ppm, cobalt 61.98 ppm, and molybdenum 31.36 ppm, much higher than the levels found in the general population. A decrease in the levels of chromium (43.8%), molybdenum (51.1%), and cobalt (91.1%) was observed at one year in the patients who had further surgery to remove the prosthesis. High concentrations of metals in the hair are observed in hip replacements with metal-metal friction, which decrease when that implant is removed. The determination of metal ions in hair could be a good marker of the metal poisoning that occurs in these arthroplasty models. Copyright © 2014 SECOT. Published by Elsevier Espana. All rights reserved.

  4. Laccase Immobilization by Chelated Metal Ion Coordination Chemistry

    Directory of Open Access Journals (Sweden)

    Qingqing Wang

    2014-09-01

    Full Text Available In this work, amidoxime polyacrylonitrile (AOPAN nanofibrous membrane was prepared by a reaction between PAN nanofibers and hydroxylamine hydrochloride. The AOPAN nanofibrous membranes were used for four metal ions (Fe3+, Cu2+, Ni2+, Cd2+ chelation under different conditions. Further, the competition of different metal ions coordinating with AOPAN nanofibrous membrane was also studied. The AOPAN chelated with individual metal ion (Fe3+, Cu2+, Ni2+, Cd2+ and also the four mixed metal ions were further used for laccase (Lac immobilization. Compared with free laccase, the immobilized laccase showed better resistance to pH and temperature changes as well as improved storage stability. Among the four individual metal ion chelated membranes, the stability of the immobilized enzymes generally followed the order as Fe–AOPAN–Lac > Cu–AOPAN–Lac > Ni–AOPAN–Lac > Cd–AOPAN–Lac. In addition, the immobilized enzyme on the carrier of AOPAN chelated with four mixed metal ions showed the best properties.

  5. Enhancement of metal bioleaching from contaminated sediment using silver ion.

    Science.gov (United States)

    Chen, Shen-Yi; Lin, Jih-Gaw

    2009-01-30

    A silver-catalyzed bioleaching process was used to remove heavy metals from contaminated sediment in this study. The effects of silver concentration added on the performance of bioleaching process were investigated. High pH reduction rate was observed in the bioleaching process with silver ion. The silver ion added in the bioleaching process was incorporated into the lattice of the initial sulfide through a cationic interchange reaction. This resulted in the short lag phase and high metal solubilization in the bioleaching process. The maximum pH reduction rate and the ideal metal solubilization were obtained in the presence of 30 mg/L of silver ion. When the added silver ion was greater than 30 mg/L, the rates of pH reduction and metal solubilization gradually decreased. The solubilization efficiencies of heavy metals (Cu, Zn, Mn, Ni and Cr) were relatively high in the silver-enhanced bioleaching process, except Pb. No apparent effect of silver ion on the growth of sulfur-oxidizing bacteria was found in the bioleaching. These results indicate that the kinetics of metal solubilization can be enhanced by the addition of silver ion.

  6. Chromatographic separation process with pellicular ion exchange resins that can be used for ion or isotope separation and resins used in this process

    International Nuclear Information System (INIS)

    Carles, M.; Neige, R.; Niemann, C.; Michel, A.; Bert, M.; Bodrero, S.; Guyot, A.

    1989-01-01

    For separation of uranium, boron or nitrogen isotopes, an isotopic exchange is carried out betwen an isotope fixed on an ion exchange resin and another isotope of the same element in the liquid phase contacting the resin. Pellicular resins are used comprising composite particulates with an inert polymeric core and a surface layer with ion exchange groups [fr

  7. Chemical Speciation of Some metal ions in Groundwaters of Yola ...

    African Journals Online (AJOL)

    Chemical speciation of some metal ions in groundwaters of Yola area using geochemical model were carried out to determine the water quality of the area using the PHREEQC speciation model. The study findings based on model calculations indicated that free Na+, Ca2+, Mg2+ and K+ ions are present and the ...

  8. Electrical properties of polymer modified by metal ion implantation

    International Nuclear Information System (INIS)

    Wu Yuguang; Zhang Tonghe; Zhang Huixing; Zhang Xiaoji; Deng Zhiwei; Zhou Gu

    2000-01-01

    Polyethylene terephthalate (PET) has been modified by Ag, Cr, Cu and Si ion implantation with a dose range from 1x10 16 to 2x10 17 ions cm -2 using a metal vapor vacuum arc (MEVVA) source. The electrical properties of PET have been changed after metal ion implantation. The resistivity of implanted PET decreased obviously with an increase of ion dose. When metal ion dose of 2x10 17 cm -2 was selected, the resistivity of PET could be less than 10 Ω cm, but when Si ions are implanted, the resistivity of PET would be up to several hundred Ω cm. The results show that the conductive behavior of a metal ion implanted sample is obviously different from Si implantation one. The changes of the structure and composition have been observed with transmission electron microscope (TEM) and X-ray diffraction (XRD). The surface structure is varying after ion implantation and it is believed that the change would cause the improvement of the conductive properties. The mechanism of electrical conduction will be discussed

  9. Effect of ion beam irradiation on metal particle doped polymer ...

    Indian Academy of Sciences (India)

    that the surface roughness increases after ion beam irradiation. Keywords. Composite materials; ion beam irradiation; dielectric properties; X-ray diffraction. 1. Introduction. Various metal fillers were incorporated in polymers to pro- duce novel functionalized composites, which have found extensive applications, such as ...

  10. The kinetics and thermodynamics of adsorption of heavy metal ions ...

    African Journals Online (AJOL)

    Titanium-Pillared and Un-Pillared bentonite clays were studied in order to evaluate the thermodynamics and kinetics of heavy metal ion removal from aqueous solutions. The results showed that the maximum sorption of Cu, Cd, Hg and Pb ions occurred within 30 minutes. A pseudo-second order kinetic model was used to ...

  11. Sorption of toxic metal ions in aqueous environment using ...

    African Journals Online (AJOL)

    2012-03-08

    Mar 8, 2012 ... efficient sorbents for divalent heavy metal ions in aqueous environments as their efficiencies exceeded those of chitosan microspheres, ion-imprinted composites, ..... field strength of 1.67 kV/cm. Under these optimised condi- ..... extraction on modified multiwalled carbon nanotubes. Cent. Eur. J. Chem.

  12. Quantum ion-acoustic wave oscillations in metallic nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Moradi, Afshin, E-mail: a.moradi@kut.ac.ir [Department of Engineering Physics, Kermanshah University of Technology, Kermanshah, Iran and Department of Nano Sciences, Institute for Studies in Theoretical Physics and Mathematics (IPM), Tehran (Iran, Islamic Republic of)

    2015-05-15

    The low-frequency electrostatic waves in metallic nanowires are studied using the quantum hydrodynamic model, in which the electron and ion components of the system are regarded as a two-species quantum plasma system. The Poisson equation as well as appropriate quantum boundary conditions give the analytical expressions of dispersion relations of the surface and bulk quantum ion-acoustic wave oscillations.

  13. Two-photon-induced reduction of metal ions for fabricating three-dimensional electrically conductive metallic microstructure

    Science.gov (United States)

    Tanaka, Takuo; Ishikawa, Atsushi; Kawata, Satoshi

    2006-02-01

    We developed techniques for fabricating three-dimensional metallic microstructures using two-photon-induced metal-ion reduction. In this process, ions in a metal-ion aqueous solution were directly reduced by a tightly focused femtosecond pulsed laser to fabricate arbitrary three-dimensional structures. A self-standing metallic microstructure with high electrical conductivity was demonstrated.

  14. FTIR spectroscopy structural analysis of the interaction between Lactobacillus kefir S-layers and metal ions

    Science.gov (United States)

    Gerbino, E.; Mobili, P.; Tymczyszyn, E.; Fausto, R.; Gómez-Zavaglia, A.

    2011-02-01

    FTIR spectroscopy was used to structurally characterize the interaction of S-layer proteins extracted from two strains of Lactobacillus kefir (the aggregating CIDCA 8348 and the non-aggregating JCM 5818) with metal ions (Cd +2, Zn +2, Pb +2 and Ni +2). The infrared spectra indicate that the metal/protein interaction occurs mainly through the carboxylate groups of the side chains of Asp and Glut residues, with some contribution of the NH groups belonging to the peptide backbone. The frequency separation between the νCOO - anti-symmetric and symmetric stretching vibrations in the spectra of the S-layers in presence of the metal ions was found to be ca. 190 cm -1 for S-layer CIDCA 8348 and ca. 170 cm -1 for JCM 5818, denoting an unidentate coordination in both cases. Changes in the secondary structures of the S-layers induced by the interaction with the metal ions were also noticed: a general trend to increase the amount of β-sheet structures and to reduce the amount of α-helices was observed. These changes allow the proteins to adjust their structure to the presence of the metal ions at minimum energy expense, and accordingly, these adjustments were found to be more important for the bigger ions.

  15. Fluorescence array-based sensing of metal ions using conjugated polyelectrolytes.

    Science.gov (United States)

    Wu, Yi; Tan, Ying; Wu, Jiatao; Chen, Shangying; Chen, Yu Zong; Zhou, Xinwen; Jiang, Yuyang; Tan, Chunyan

    2015-04-01

    Array-based sensing offers several advantages for detecting a series of analytes with common structures or properties. In this study, four anionic conjugated polyelectrolytes (CPEs) with a common poly(p-pheynylene ethynylene) (PPE) backbone and varying pendant ionic side chains were designed. The conjugation length, repeat unit pattern, and ionic side chain composition were the main factors affecting the fluorescence patterns of CPE polymers in response to the addition of different metal ions. Eight metal ions, including Pb(2+), Hg(2+), Fe(3+), Cr(3+), Cu(2+), Mn(2+), Ni(2+), and Co(2+), categorized as water contaminants by the Environmental Protection Agency, were selected as analytes in this study. Fluorescence intensity response patterns of the four-PPE sensor array toward each of the metal ions were recorded, analyzed, and transformed into canonical scores using linear discrimination analysis (LDA), which permitted clear differentiation between metal ions using both two-dimensional and three-dimensional graphs. In particular, the array could readily differentiate between eight toxic metal ions in separate aqueous solutions at 100 nM. Our four-PPE sensor array also provides a practical application to quantify Pb(2+) and Hg(2+) concentrations in blind samples within a specific concentration range.

  16. [Metal ions: important co-players in aseptic loosening].

    Science.gov (United States)

    Cadosch, D; Schlett, C L; Gautschi, O P; Frei, H C; Filgueira, L

    2010-08-01

    The aims of this review were to discuss the different mechanisms of biocorrosion of orthopaedic metal implants in the human body, as well as the effects of the released metal ions on bone metabolism and the immune system in regard to their involvement in the pathophysiological mechanisms of aseptic loosening and metal hypersensitivity. Implant failure due to aseptic loosening is thought to occur in about 10-15% of cases. A review of the literature (using PubMed with the search terms: biocorrosion, metal ions and bone metabolism) was performed. Additionally, we discuss our research results in the field of aseptic loosening. Despite a great effort in developing new implants, metal devices used in orthopaedic and trauma surgery remain prone to biocorrosion by several mechanisms including the direct corrosion by osteoclasts, leading to the production of significant amounts of wear particles and metal ions. In addition to the well documented increased osteolytic activity caused by large (in the nanometer range) wear particles, increasing evidence strongly suggests that the released metal ions contribute to the pathophysiological mechanism of aseptic loosening. Metal ions stimulate both the immune system and bone metabolism through a series of direct and indirect pathways leading to an increased osteolytic activity at the bone-implant interface. To date, revision surgery remains the only option for the treatment of a failed orthopaedic implant caused by aseptic loosening. A better understanding of the complex pathophysiological mechanisms (including the effects caused by the released metal ions) of aseptic loosening may have a significant potential in developing novel implants and therapies in order to reduce the incidence of this complication. Georg Thieme Verlag KG Stuttgart, New York.

  17. Structural Metals in the Group I Intron: A Ribozyme with a Multiple Metal Ion Core

    Energy Technology Data Exchange (ETDEWEB)

    Stahley,M.; Adams, P.; Wang, J.; Strobel, S.

    2007-01-01

    Metal ions play key roles in the folding and function for many structured RNAs, including group I introns. We determined the X-ray crystal structure of the Azoarcus bacterial group I intron in complex with its 5' and 3' exons. In addition to 222 nucleotides of RNA, the model includes 18 Mg2+ and K+ ions. Five of the metals bind within 12 Angstroms of the scissile phosphate and coordinate the majority of the oxygen atoms biochemically implicated in conserved metal-RNA interactions. The metals are buried deep within the structure and form a multiple metal ion core that is critical to group I intron structure and function. Eight metal ions bind in other conserved regions of the intron structure, and the remaining five interact with peripheral structural elements. Each of the 18 metals mediates tertiary interactions, facilitates local bends in the sugar-phosphate backbone or binds in the major groove of helices. The group I intron has a rich history of biochemical efforts aimed to identify RNA-metal ion interactions. The structural data are correlated to the biochemical results to further understand the role of metal ions in group I intron structure and function.

  18. DETERMINATION OF METAL IONS RELEASED BY STAINLESS ...

    African Journals Online (AJOL)

    The amounts of cobalt, iron, manganese, nickel and chromium ions released from new and reused stainless steel arch bar used for maxillomandibular fixation was determined in Hank's solutions of different hydrogen and chloride ions concentrations, whole blood serum and phosphate buffered saline (PBS) in vitro, over a ...

  19. Separation of the metallic and non-metallic fraction from printed circuit boards employing green technology

    Energy Technology Data Exchange (ETDEWEB)

    Estrada-Ruiz, R.H., E-mail: rhestrada@itsaltillo.edu.mx; Flores-Campos, R., E-mail: rcampos@itsaltillo.edu.mx; Gámez-Altamirano, H.A., E-mail: hgamez@itsaltillo.edu.mx; Velarde-Sánchez, E.J., E-mail: ejvelarde@itsaltillo.edu.mx

    2016-07-05

    Highlights: • Small sizes of particles are required in order to separate the different fractions. • Inverse flotation process is an efficient green technology to separate fractions. • Superficial air velocity is the main variable in the inverse flotation process. • Inverse flotation is a green process because the pulṕs pH is 7.0 during the test. - Abstract: The generation of electrical and electronic waste is increasing day by day; recycling is attractive because of the metallic fraction containing these. Nevertheless, conventional techniques are highly polluting. The comminution of the printed circuit boards followed by an inverse flotation process is a clean technique that allows one to separate the metallic fraction from the non-metallic fraction. It was found that particle size and superficial air velocity are the main variables in the separation of the different fractions. In this way an efficient separation is achieved by avoiding the environmental contamination coupled with the possible utilization of the different fractions obtained.

  20. A novel metal ion source for preparing hard coatings

    International Nuclear Information System (INIS)

    Feng, Y.C.; Wong, S.P.

    1999-01-01

    A novel metal ion source, Electron Beam Evaporation Metal Ion Source, has been developed for material modifications. This ion source is based on the electron beam evaporation technology. It can provide gaseous, solid or gaseous and solid mixed intense ion beams for preparing a variety of thin films. In this ion source, a focusing electron beam is used to bombard and vaporize the metal or other solid element within same chamber where the metal or solid atoms are ionized and plasma medium from which ions are extracted is formed by arc discharge. A small aperture diameter extraction system is used for extracting the ion beam from this source. Ion beams of a series of elements, which include C, W, Ta, Mo, Cr, Ti, B, Cu, Ni, Al, Ar, N, C+N, Ti+N, Cr+N, etc., have been extracted. The source has a 3.6 cm extraction diameter. The beam energy ranges from 0.3 to 4 keV for single charge state ions, and the maximum beam current extractable is over 90 mA. The source has been used for preparing hard coatings. The films of carbon nitride and titanium nitride have been synthesized by direct deposition with C+N and Ti+N mixed ion beams. The results have shown to exhibit very high hardness value for carbon nitride films. The microhardness is up to HK 5800 kgf/mm 2 . In comparison with other methods, it is also to exhibit higher hardness value for titanium nitride coating. The highest hardness value obtained for titanium nitride is about 3000 kgf/mm 2 . The AES profile shows that there is a good intermixture between coating and substrate for both films. The principle, structure and performance of this ion source will be described. The preliminary results for forming hard coatings are also presented in this article

  1. Heavy metal ion adsorption onto polypyrrole-impregnated porous carbon.

    Science.gov (United States)

    Choi, Moonjung; Jang, Jyongsik

    2008-09-01

    Polypyrrole-impregnated porous carbon was readily synthesized using vapor infiltration polymerization of pyrrole monomers. The results show that the functionalized polymer layer was successfully coated onto the pore surface of carbon without collapse of mesoporous structure. The modified porous carbon exhibited an improved complexation affinity for heavy metal ions such as mercury, lead, and silver ions due to the amine group of polypyrrole. The introduced polypyrrole layer could provide the surface modification to be applied for heavy metal ion adsorbents. Especially, polymer-impregnated porous carbon has an enhanced heavy metal ion uptake, which is 20 times higher than that of adsorbents with amine functional groups. Furthermore, the relationship between the coated polymer amount and surface area was also investigated in regard to adsorption capacity.

  2. Investigation of metal ions sorption of brown peat moss powder

    Science.gov (United States)

    Kelus, Nadezhda; Blokhina, Elena; Novikov, Dmitry; Novikova, Yaroslavna; Chuchalin, Vladimir

    2017-11-01

    For regularities research of sorptive extraction of heavy metal ions by cellulose and its derivates from aquatic solution of electrolytes it is necessary to find possible mechanism of sorption process and to choice a model describing this process. The present article investigates the regularities of aliovalent metals sorption on brown peat moss powder. The results show that sorption isotherm of Al3+ ions is described by Freundlich isotherm and sorption isotherms of Na+ i Ni2+ are described by Langmuir isotherm. To identify the mechanisms of brown peat moss powder sorption the IR-spectra of the initial brown peat moss powder samples and brown peat moss powder samples after Ni (II) sorption were studied. Metal ion binding mechanisms by brown peat moss powder points to ion exchange, physical adsorption, and complex formation with hydroxyl and carboxyl groups.

  3. The separation of heavy ion tracks in nuclear emulsions by means of the pulsed electric field

    International Nuclear Information System (INIS)

    Akopova, A.B.; Magradze, N.V.; Melkumyan, L.V.; Prokhorenko, Y.P.

    1976-01-01

    The pulsed electric field (PEF) technique is developed for the separation of heavy ion tracks from the intense background caused by high energy electrons, protons and γ-radiation. The tracks of Ne, Cr, Ar-ions accelerated at the Dubna Nuclear Reactions Laboratory have been separated from the background, the voltage of the applied PEF being 10 5 V/cm. (orig.) [de

  4. Standard practice for The separation of americium from plutonium by ion exchange

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2001-01-01

    1.1 This practice describes the use of an ion exchange technique to separate plutonium from solutions containing low concentrations of americium prior to measurement of the 241Am by gamma counting. 1.2 This practice covers the removal of plutonium, but not all the other radioactive isotopes that may interfere in the determination of 241Am. 1.3 This practice can be used when 241Am is to be determined in samples in which the plutonium is in the form of metal, oxide, or other solid provided that the solid is appropriately sampled and dissolved (See Test Methods C758, C759, and C1168). 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  5. Immobilised Metal Affinity Chromatography (IMAC) Beads for Lysozyme Separation: Synthesis and Characterization Study

    International Nuclear Information System (INIS)

    Fatin Mohd Nasir; Sofiah Hamzah; Amirah Hamzah; Nora'aini Ali; Marinah Mohd Ariffin

    2016-01-01

    Immobilized metal affinity chromatography (IMAC) has been established as a highly specific chromatographic technique for the production of enzymes and proteins including lysozyme. This study aimed to prepare and characterize the IMAC beads for lysozyme separation. Silica gel served as chromatographic matrix which has been coated with chitosan layer and crosslinked with glutaraldehyde (GTA-CTS-SiO 2 ) since it is very convenient to promote fixation. Various IMAC ligands were immobilized by chelating 1500 mg/ l Cu 2+ , Zn 2+ , Fe 2+ , Fe 3+ and Al 3+ ions, respectively on GTA-CTS-SiO 2 . IMAC which was immobilized with 1200mg/ l Cu 2+ exhibited the maximal immobilization capacity (27.08mg/ g) of within 30 minutes incubation time. This fundamental study can be a momentous pathway to develop an efficient chromatographic system for lysozyme separation in the future. (author)

  6. Accumulation of some metal ions on Bacillus licheniformis

    International Nuclear Information System (INIS)

    Hafez, M.B.; El-Desouky, W.; Fouad, A.

    2001-01-01

    Pure species of Bacillus licheniformis was used to remove ions from aqueous and simulated waste solutions. Metal ion accumulation on B. licheniformis was fast. Maximum uptake occurred at pH 4± 0.5 and at 25 ± 3 deg C. One gram of dry B. licheniformis was found to accumulate 115 mg cerium, 34 mg copper and 11 mg cobalt from aqueous solutions. The presence of certain foreign ions such as calcium, sodium and potassium decreased the uptake of ions by B. licheniformis, while citrate and EDTA prevent the uptake. Electron microscopic investigations showed that cerium (III), copper (II) and cobalt (II) accumulated extracellulary around the surface wall of B. licheniformis cells. A bio-adsorption mechanism between the metal ions and B. licheniformis cell wall was proposed. (author)

  7. High efficiency noble gas electron impact ion source for isotope separation

    Energy Technology Data Exchange (ETDEWEB)

    Appelhans, A. D. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Olson, J. E. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Dahl, D. A. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Ward, M. B. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2016-07-01

    An electron impact ion source has been designed for generation of noble gas ions in a compact isotope separator. The source utilizes a circular filament that surrounds an ionization chamber, enabling multiple passes of electrons through the ionization chamber. This report presents ion optical design and the results of efficiency and sensitivity measurements performed in an ion source test chamber and in the compact isotope separator. The cylindrical design produced xenon ions at an efficiency of 0.37% with a sensitivity of ~24 µA /Pa at 300 µA of electron current.

  8. Method and electrochemical cell for synthesis and treatment of metal monolayer electrocatalysts metal, carbon, and oxide nanoparticles ion batch, or in continuous fashion

    Science.gov (United States)

    Adzic, Radoslav; Zhang, Junliang; Sasaki, Kotaro

    2015-04-28

    An apparatus and method for synthesis and treatment of electrocatalyst particles in batch or continuous fashion is provided. In one embodiment, the apparatus comprises a sonication bath and a two-compartment chamber submerged in the sonication bath. The upper and lower compartments are separated by a microporous material surface. The upper compartment comprises a cover and a working electrode (WE) connected to a Pt foil contact, with the foil contact connected to the microporous material. The upper chamber further comprises reference counter electrodes. The lower compartment comprises an electrochemical cell containing a solution of metal ions. In one embodiment, the method for synthesis of electrocatalysts comprises introducing a plurality of particles into the apparatus and applying sonication and an electrical potential to the microporous material connected to the WE. After the non-noble metal ions are deposited onto the particles, the non-noble metal ions are displaced by noble-metal ions by galvanic displacement.

  9. Modeling of hydrogen isotopes separation in a metal hydride bed

    International Nuclear Information System (INIS)

    Charton, S.; Corriou, J.P.; Schweich, D.

    1999-01-01

    A predictive model for hydrogen isotopes separation in a non-isothermal bed of unsupported palladium hydride particles is derived. It accounts for the non-linear adsorption-dissociation equilibrium, hydrodynamic dispersion, pressure drop, mass transfer kinetics, heat of sorption and heat losses at the bed wall. Using parameters from the literature or estimated with classical correlations, the model gives simulated curves in agreement with previously published experiments without any parameter fit. The non-isothermal behavior is shown to be responsible for drastic changes of the mass transfer rate which is controlled by diffusion in the solid-phase lattice. For a feed at 300 K and atmospheric pressure, the endothermic hydride-to-deuteride exchange is kinetically controlled, whereas the reverse exothermic exchange is nearly at equilibrium. Finally, a simple and efficient thermodynamic model for the dissociative equilibrium between a metal and a diatomic gas is proposed. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

  10. Recovery of precious metals from industrial wastes using membrane separation

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Jin Ki; Lee, Jae Chun; Youn, In Ju [Korea Inst. of Geology Mining and Materials, Taejon (Korea, Republic of)

    1995-12-01

    The purpose of the research is to develop a membrane technology for the recovery of Au by the concentration of used cyanide solution. Au and Ag have been widely used in various advanced technology due to their excellent physical and chemical properties. In most of their application, they were electrodeposited in the cyanide solution. The solution was also used as an etchant for the decorative gold alloys such as 14 K and 18 K. Due to the expanding related industry, the amount of used cyanide solution has been greatly increased. The used solution normally contains about 1-3 g/1 of Au. Due to their high prices various separation method has been developed and commercialized for long time. The concentration method which removes water offers various advantages like the reduction of used solution, the needless of additional cyanide, and the increase in the recovery rate. The main objective of the study was laid in the development of an economical recovery process for precious metals including Au from used cyanide solution. To achieve this goal related processes were reviewed comprehensively focussing on the membrane process and the concentration process. The feasibility of membrane process was evaluated by the measurement of separation efficiency and concentration efficiency of cyanide. In addition, various CN analysis was compared in order to develop a simple and routine procedure for future experiment. The process does not require additional cyanide and thus prevents further environmental contamination. It is economical because the recovery can be increased by the concentration of the solution during the recovery process. In addition, it can be applied to other metals waste system due to the reduced recovery process by concentration. The used water can also be reused. (author). 23 refs., 16 figs., 5 tabs.

  11. Metal ions potentiate microglia responsiveness to endotoxin.

    Science.gov (United States)

    Rachmawati, Dessy; Peferoen, Laura A N; Vogel, Daphne Y S; Alsalem, Inás W A; Amor, Sandra; Bontkes, Hetty J; von Blomberg, B Mary E; Scheper, Rik J; van Hoogstraten, Ingrid M W

    2016-02-15

    Oral metal exposure has been associated with diverse adverse reactions, including neurotoxicity. We showed previously that dentally applied metals activate dendritic cells (MoDC) via TLR4 (Ni, Co, Pd) and TLR3 (Au). It is still unknown whether the low levels of dental metals reaching the brain can trigger local innate cells or prime them to become more responsive. Here we tested whether dentally applied metals (Cr, Fe, Co, Ni, Cu, Zn, Au, Hg) activate primary human microglia in vitro and, as a model, monocytic THP-1-cells, in high non-toxic as well as near-physiological concentrations. In addition the effects of 'near-physiological' metal exposure on endotoxin (LPS) responsiveness of these cells were evaluated. IL-8 and IL-6 production after 24h was used as read out. In high, non-toxic concentrations all transition metals except Cr induced IL-8 and IL-6 production in microglia, with Ni and Co providing the strongest stimulation. When using near-physiological doses (up to 10× the normal plasma concentration), only Zn and Cu induced significant IL-8 production. Of note, the latter metals also markedly potentiated LPS responsiveness of microglia and THP-1 cells. In conclusion, transition metals activate microglia similar to MoDCs. In near-physiological concentrations Zn and Cu are the most effective mediators of innate immune activation. A clear synergism between innate responses to Zn/Cu and LPS was observed, shedding new light on the possible relation between oral metal exposure and neurotoxicity. Copyright © 2015. Published by Elsevier B.V.

  12. Determination of uranium and rare-earth metals separation coefficients in LiCl-KCl melt by electrochemical transient techniques

    Energy Technology Data Exchange (ETDEWEB)

    Kuznetsov, S.A. [Institute of Chemistry, Kola Science Centre, RAS, 184200 Apatity, Murmansk Region (Russian Federation)]. E-mail: kuznet@chemy.kolasc.net.ru; Hayashi, H. [Japan Atomic Energy Research Institute, Tokai-mura, Naka-gun, Ibaraki-ken 319-1195 (Japan); Minato, K. [Japan Atomic Energy Research Institute, Tokai-mura, Naka-gun, Ibaraki-ken 319-1195 (Japan); Gaune-Escard, M. [Ecole Polytechnique, IUSTI-CNRS UMR 6595, Technopole de Chateau Gombert, F-13453 Marseille cedex 13 (France)

    2005-09-01

    The main step in the pyrometallurgical process of spent nuclear fuel recycling is a molten salt electrorefining. The knowledge of separation coefficients of actinides (U, Np, Pu and Am) and rare-earth metals (Y, La, Ce, Nd and Gd) is very important for this step. Usually the separation coefficients are evaluated from the formal standard potentials of metals in melts containing their own ions, values obtained by potentiometric method. Electrochemical experiments were carried out at 723-823 K in order to estimate separation coefficients in LiCl-KCl eutectic melt containing uranium and lanthanum trichlorides. It was shown that for the calculation of uranium and lanthanum separation coefficients it is necessary to determine the voltammetric peak potentials of U(III) and La(III), their concentration in the melt and the kinetic parameters relating to U(III) discharge such as transfer and diffusion coefficients, and standard rate constants of charge transfer.

  13. Determination of uranium and rare-earth metals separation coefficients in LiCl KCl melt by electrochemical transient techniques

    Science.gov (United States)

    Kuznetsov, S. A.; Hayashi, H.; Minato, K.; Gaune-Escard, M.

    2005-09-01

    The main step in the pyrometallurgical process of spent nuclear fuel recycling is a molten salt electrorefining. The knowledge of separation coefficients of actinides (U, Np, Pu and Am) and rare-earth metals (Y, La, Ce, Nd and Gd) is very important for this step. Usually the separation coefficients are evaluated from the formal standard potentials of metals in melts containing their own ions, values obtained by potentiometric method. Electrochemical experiments were carried out at 723-823 K in order to estimate separation coefficients in LiCl-KCl eutectic melt containing uranium and lanthanum trichlorides. It was shown that for the calculation of uranium and lanthanum separation coefficients it is necessary to determine the voltammetric peak potentials of U(III) and La(III), their concentration in the melt and the kinetic parameters relating to U(III) discharge such as transfer and diffusion coefficients, and standard rate constants of charge transfer.

  14. Metal ion coupled protein folding and allosteric motions

    Science.gov (United States)

    Wang, Wei

    2014-03-01

    Many proteins need the help of cofactors for their successful folding and functioning. Metal ions, i.e., Zn2+, Ca2+, and Mg2+ etc., are typical biological cofactors. Binding of metal ions can reshape the energy landscapes of proteins, thereby modifying the folding and allosteric motions. For example, such binding may make the intrinsically disordered proteins have funneled energy landscapes, consequently, ensures their spontaneous folding. In addition, the binding may activate certain biological processes by inducing related conformational changes of regulation proteins. However, how the local interactions involving the metal ion binding can induce the global conformational motions of proteins remains elusive. Investigating such question requires multiple models with different details, including quantum mechanics, atomistic models, and coarse grained models. In our recent work, we have been developing such multiscale methods which can reasonably model the metal ion binding induced charge transfer, protonation/deprotonation, and large conformational motions of proteins. With such multiscale model, we elucidated the zinc-binding induced folding mechanism of classical zinc finger and the calcium-binding induced dynamic symmetry breaking in the allosteric motions of calmodulin. In addition, we studied the coupling of folding, calcium binding and allosteric motions of calmodulin domains. In this talk, I will introduce the above progresses on the metal ion coupled protein folding and allosteric motions. We thank the finacial support from NSFC and the 973 project.

  15. Adsorption of heavy metal ions by sawdust of deciduous trees.

    Science.gov (United States)

    Bozić, D; Stanković, V; Gorgievski, M; Bogdanović, G; Kovacević, R

    2009-11-15

    The adsorption of heavy metal ions from synthetic solutions was performed using sawdust of beech, linden and poplar trees. The adsorption depends on the process time, pH of the solution, type of ions, initial concentration of metals and the sawdust concentration in suspension. The kinetics of adsorption was relatively fast, reaching equilibrium for less than 20 min. The adsorption equilibrium follows Langmuir adsorption model. The ion exchange mechanism was confirmed assuming that the alkali-earth metals from the adsorbent are substituted by heavy metal ions and protons. On lowering the initial pH, the adsorption capacity decreased, achieving a zero value at a pH close to unity. The maximum adsorption capacity (7-8 mg g(-1) of sawdust) was achieved at a pH between 3.5 and 5 for all the studied kinds of sawdust. The initial concentration of the adsorbate and the concentration of sawdust strongly affect the process. No influence of particles size was evidenced. A degree of adsorption higher than 80% can be achieved for Cu(2+) ions but it is very low for Fe(2+) ions, not exceeding 10%.

  16. Adsorption of heavy metal ions by sawdust of deciduous trees

    International Nuclear Information System (INIS)

    Bozic, D.; Stankovic, V.; Gorgievski, M.; Bogdanovic, G.; Kovacevic, R.

    2009-01-01

    The adsorption of heavy metal ions from synthetic solutions was performed using sawdust of beech, linden and poplar trees. The adsorption depends on the process time, pH of the solution, type of ions, initial concentration of metals and the sawdust concentration in suspension. The kinetics of adsorption was relatively fast, reaching equilibrium for less than 20 min. The adsorption equilibrium follows Langmuir adsorption model. The ion exchange mechanism was confirmed assuming that the alkali-earth metals from the adsorbent are substituted by heavy metal ions and protons. On lowering the initial pH, the adsorption capacity decreased, achieving a zero value at a pH close to unity. The maximum adsorption capacity (7-8 mg g -1 of sawdust) was achieved at a pH between 3.5 and 5 for all the studied kinds of sawdust. The initial concentration of the adsorbate and the concentration of sawdust strongly affect the process. No influence of particles size was evidenced. A degree of adsorption higher than 80% can be achieved for Cu 2+ ions but it is very low for Fe 2+ ions, not exceeding 10%.

  17. Ion conducting fluoropolymer carbonates for alkali metal ion batteries

    Science.gov (United States)

    DeSimone, Joseph M.; Pandya, Ashish; Wong, Dominica; Balsara, Nitash P.; Thelen, Jacob; Devaux, Didier

    2017-09-05

    Liquid or solid electrolyte compositions are described that comprise a homogeneous solvent system and an alkali metal salt dissolved in said solvent system. The solvent system may comprise a fluoropolymer, having one or two terminal carbonate groups covalently coupled thereto. Batteries containing such electrolyte compositions are also described.

  18. The solvent extraction of alkali metal ions with β-diketones

    International Nuclear Information System (INIS)

    Munakata, Megumu; Niina, Syozo; Shimoji, Noboru

    1974-01-01

    This work was undertaken to investigate effects of solvent and chelating-agent on the solvent extraction of alkali metal ions by seven β-diketones, acetylacetone (Acac), benzoylacetone (BzA), dipivaloylmethane (DPM), dibenzoylmethane (DBM), thenoyltrifluoloacetone (TTA), benzoyltrifluoroacetone (BFA) and hexafluoroacetylacetone (HFA), and to separate lithium from alkali metals. The extraction of alkali metals increase with increasing donor power of the solvent: i.e., benzene Na>K>Rb>Cs, which is also the order in which the adduct formation of these β-diketone chelates with donor solvents increase. The adduct formations between β-diketone chelates of alkali metals and donor solvents markedly enhance the solubilities of the chelates in solvents and, consequently, the extractabilities of alkali metals with β-diketones. Lithium was extracted with TTA in ether at such a low base concentration that sodium, potassium, rubidium and cesium were hardly extracted, and this enabled to separate lithium from other metals by the use of rubidium hydroxide (0.02 M). An attempt has been made to isolate alkali metal β-diketone chelates and some chelates have been obtained as crystals. The infrared absorption bands arising from C=O and C.=C of TTA shift to lower frequencies in the alkali metal chelates with TTA, and consequently, β-diketones is suggested to coordinate to alkali metal as a bidentate ligand. (JPN)

  19. ANION EXCHANGE METHOD FOR SEPARATION OF METAL VALUES

    Science.gov (United States)

    Hyde, E.K.; Raby, B.A.

    1959-02-10

    A method is described for selectively separating radium, bismuth, poloniums and lead values from a metallic mixture of thc same. The mixture is dissolved in aqueous hydrochloric acid and the acidity is adjusted to between 1 to 2M in hydrochloric acid to form the anionic polychloro complexes of polonium and bismuth. The solution is contacted with a first anion exchange resin such as strong base quaternary ammonia type to selectively absorb the polonium and bismuth leaving the radium and lead in the effluent. The effluent, after treatment in hydrochloric acid to increase the hydrochloric acid concentration to 6M is contacted with a second anion exchange iesin of the same type as the above to selectively adsorb the lead leaving the radium in the effluent. Radium is separately recovered from the effluent from the second exchange column. Lead is stripped from the loaded resin of the second column by treatment with 3M hydrochloric acid solution. The loaded resin of the first column is washed with 8M hydrochloric acid solution to recover bismuth and then treated with strong nitric acid solution to recover polonium.

  20. {sup 55}Co separation from proton irradiated metallic nickel

    Energy Technology Data Exchange (ETDEWEB)

    Valdovinos, H. F., E-mail: hvaldovinos@wisc.edu; Graves, S., E-mail: hvaldovinos@wisc.edu; Barnhart, T., E-mail: hvaldovinos@wisc.edu; Nickles, R. J., E-mail: hvaldovinos@wisc.edu [Department of Medical Physics, University of Wisconsin - Madison, Madison, WI (United States)

    2014-11-07

    {sup 55}Co with > 97% radionuclidic purity 24 hours after end of bombardment (EoB) was produced from the {sup 58}Ni(p,α) reaction using proton irradiations of 16 MeV on natural nickel. Two-hour irradiations with 25 μA on a 254 μm thick nickel foil generate 0.18 ± 0.01 GBq (n = 3) 24 hours after EoB. The separation of cobalt from the target material and other metallic contaminants present at trace levels is accomplished in HCl medium by two rounds of anion exchange chromatography (AG1-X8) using an automated module driven by a peristaltic pump. 80 ± 5 % (n = 3) of the activity generated at EoB is ready for labeling in 0.1 M HCl one hour after the start of separation. Using 99.999% pure Ni, the reactivity (decay corrected to EoB) with the bifunctional chelator (BFC) DOTA was 8.5 GBq/μmol; enough for radiolabeling BFC conjugated biomolecules at a nmol scale with > 90% yield. Using 99.9% pure Ni the reactivity with DOTA and NOTA was 0.19 +/− 0.09 GBq/μmol and 2.9 +/− 1.7 GBq/μmol (n = 2), respectively. Both cobalt complexes showed 100% in vitro stability in PBS and mouse serum over 41 hours at room temperature. MicroPET images of a miniature Derenzo phantom show excellent resolution where rods of 1.5 mm were separated by two times their diameter.

  1. Indirect ultraviolet detection of alkaline earth metal ions using an imidazolium ionic liquid as an ultraviolet absorption reagent in ion chromatography.

    Science.gov (United States)

    Liu, Yong-Qiang; Yu, Hong

    2017-04-01

    A convenient and versatile method was developed for the separation and detection of alkaline earth metal ions by ion chromatography with indirect UV detection. The chromatographic separation of Mg 2+ , Ca 2+ , and Sr 2+ was performed on a carboxylic acid base cation exchange column using imidazolium ionic liquid/acid as the mobile phase, in which the imidazolium ionic liquid acted as an UV-absorption reagent. The effects of imidazolium ionic liquids, detection wavelength, acids in the mobile phase, and column temperature on the retention of Mg 2+ , Ca 2+ , and Sr 2+ were investigated. The main factors influencing the separation and detection were the background UV absorption reagent and the concentration of hydrogen ion in ion chromatography with indirect UV detection. The successful separation and detection of Mg 2+ , Ca 2+ , and Sr 2+ within 14 min were achieved using the selected chromatographic conditions, and the detection limits (S/N = 3) were 0.06, 0.12, and 0.23 mg/L, respectively. A new separation and detection method of alkaline earth metal ions by ion chromatography with indirect UV detection was developed, and the application range of ionic liquids was expanded. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Metallic ion release after knee prosthesis implantation: a prospective study.

    Science.gov (United States)

    Lons, Adrien; Putman, Sophie; Pasquier, Gilles; Migaud, Henri; Drumez, Elodie; Girard, Julien

    2017-12-01

    Metal-on-metal (MoM) hip replacement bearings produce metallic ions that can cause health complications. Metallic release also occurs with other materials, but data on metallic ion levels after knee arthroplasty are sparse. We postulate that knee replacement generates elevating metallic ions (chromium (Cr), cobalt (Co) and titanium (Ti)) during the first year after implantation. This ongoing prospective study included all patients who underwent the same type of knee arthroplasty between May and December 2013. Cr, Co and Ti levels were measured in whole blood at pre-operation and one-year follow-up (6 and 12 months). Clinical and radiographic data (range of motion, Oxford, International Knee Society (IKS) and satisfaction scores) were recorded. In 90 patients, preoperative Cr, Co and Ti metallic ion levels were respectively 0.45 μg/l, 0.22 μg/l, 2.94 μg/l and increased to 1.27 μg/l, 1.41 μg/l, 4.08 μg/l (p < 0.0001) at last one-year follow-up. Mean Oxford and IKS scores rose, respectively, from 45.9 (30-58) and 24.9 (12-52) to 88.3 (0-168) and 160.8 (93-200) (p < 0.001). After the implantation of knee arthroplasty, we found significant blood elevation of Cr, Co and Ti levels one year after implantation exceeding the normal values. This metallic ion release could lead to numerous effects: allergy, hypersensitivity, etc.

  3. Metal ion mediated photolysis reactions of riboflavin: A kinetic study.

    Science.gov (United States)

    Ahmad, Iqbal; Anwar, Zubair; Ahmed, Sofia; Sheraz, Muhammad Ali; Khattak, Saif-Ur-Rehman

    2017-08-01

    The effect of metal ion complexation on the photolysis of riboflavin (RF) using various metal ions (Ag + , Ni 2+ , Co 2+ , Fe 2+ , Ca 2+ , Cd 2+ , Cu 2+ , Mn 2+ , Pb 2+ , Mg 2+ , Zn 2+ , Fe 3+ ) has been studied. Ultraviolet and visible spectral and fluorimetric evidence has been obtained to confirm the formation of metal-RF complexes. The kinetics of photolysis of RF in metal-RF complexes at pH7.0 has been evaluated. The apparent first-order rate constant (k obs ) for the photolysis of RF and the formation of lumichrome (LC) and lumiflavin (LF) (0.001M phosphate buffer) and LC, LF and cyclodehydroriboflavin (CDRF) (0.2-0.4M phosphate buffer) have been determined. The values of k obs indicate that the rate of photolysis of RF is promoted by divalent and trivalent metal ions. The second-order rate constants (k' ) for the interaction of metal ions with RF are in the order: Zn 2+ >Mg 2+ >Pb 2+ >Mn 2+ >Cu 2+ >Cd 2+ >Fe 2+ >Ca 2+ >Fe 3+ >Co 2+ >Ni 2+ >Ag + . In phosphate buffer (0.2-0.4M), an increase in the metal ion concentration leads to a decrease in the formation of LC compared to that of CDRF by different pathways. The photoproducts of RF have been identified and RF and the photoproducts have simultaneously been assayed by a multicomponent spectrometric method. The mode of photolysis of RF in metal-RF complexes has been discussed. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. Recovery of toxic metal ions from washing effluent containing excess aminopolycarboxylate chelant in solution.

    Science.gov (United States)

    Hasegawa, Hiroshi; Rahman, Ismail M M; Nakano, Masayoshi; Begum, Zinnat A; Egawa, Yuji; Maki, Teruya; Furusho, Yoshiaki; Mizutani, Satoshi

    2011-10-15

    Aminopolycarboxylate chelants (APCs) are extremely useful for a variety of industrial applications, including the treatment of toxic metal-contaminated solid waste materials. Because non-toxic matrix elements compete with toxic metals for the binding sites of APCs, an excess of chelant is commonly added to ensure the adequate sequestration of toxic metal contaminants during waste treatment operations. The major environmental impacts of APCs are related to their ability to solubilize toxic heavy metals. If APCs are not sufficiently eliminated from the effluent, the aqueous transport of metals can occur through the introduction of APCs into the natural environment, increasing the magnitude of associated toxicity. Although several techniques that focus primarily on the degradation of APCs at the pre-release step have been proposed, methods that recycle not only the processed water, but also provide the option to recover and reuse the metals, might be economically feasible, considering the high costs involved due to the chelants used in metal ion sequestration. In this paper, we propose a separation process for the recovery of metals from effluents that contain an excess of APCs. Additionally, the option of recycling the processed water using a solid phase extraction (SPE) system with an ion-selective immobilized macrocyclic material, commonly known as a molecular recognition technology (MRT) gel, is presented. Simulated effluents containing As(V), Cd(II), Cr(III), Pb(II) or Se(IV) in the presence of APCs at molar ratios of 1:50 in H2O were studied with a flow rate of 0.2 mL min(-1). The 'captured' ions in the SPE system were quantitatively eluted with HNO3. The effects of solution pH, metal-chelant stability constants and matrix elements were assessed. Better separation performance for the metals was achieved with the MRT-SPE compared to other SPE materials. Our proposed technique offers the advantage of a non-destructive separation of both metal ions and chelants

  5. Ion beam modification of metals: Compositional and microstructural changes

    Science.gov (United States)

    Was, Gary S.

    Ion implantation has become a highly developed tool for modifying the structure and properties of metals and alloys. In addition to direct implantation, a variety of other ion beam techniques such as ion beam mixing, ion beam assisted deposition and plasma source ion implantation have been used increasingly in recent years. The modifications constitute compositional and microstructural changes in the surface of the metal. This leads to alterations in physical properties (transport, optical, corrosion, oxidation), as well as mechanical properties (strength, hardness, wear resistance, fatigue resistance). The compositional changes brought about by ion bombardment are classified into recoil implantation, cascade mixing, radiation-enhanced diffusion, radiation-induced segregation, Gibbsian adsorption and sputtering which combine to produce an often complicated compositional variation within the implanted layer and often, well beyond. Microstructurally, the phases present are often altered from what is expected from equilibrium thermodynamics giving rise to order-disorder transformations, metastable (crystalline, amorphous or quasicrystalline) phase formation and growth, as well as densification, grain growth, formation of a preferred texture and the formation of a high density dislocation network. All these effects need to be understood before one can determine the effect of ion bombardment on the physical and mechanical properties of metals. This paper reviews the literature in terms of the compositional and microstructural changes induced by ion bombardment, whether by direct implantation, ion beam mixing or other forms of ion irradiation. The topics are introduced as well as reviewed, making this a more pedogogical approach as opposed to one which treats only recent developments. The aim is to provide the tools needed to understand the consequent changes in physical and mechanical properties.

  6. Method for enhancing the resolving power of ion mobility separations over a limited mobility range

    Science.gov (United States)

    Shvartsburg, Alexandre A; Tang, Keqi; Smith, Richard D

    2014-09-23

    A method for raising the resolving power, specificity, and peak capacity of conventional ion mobility spectrometry is disclosed. Ions are separated in a dynamic electric field comprising an oscillatory field wave and opposing static field, or at least two counter propagating waves with different parameters (amplitude, profile, frequency, or speed). As the functional dependencies of mean drift velocity on the ion mobility in a wave and static field or in unequal waves differ, only single species is equilibrated while others drift in either direction and are mobility-separated. An ion mobility spectrum over a limited range is then acquired by measuring ion drift times through a fixed distance inside the gas-filled enclosure. The resolving power in the vicinity of equilibrium mobility substantially exceeds that for known traveling-wave or drift-tube IMS separations, with spectra over wider ranges obtainable by stitching multiple segments. The approach also enables low-cutoff, high-cutoff, and bandpass ion mobility filters.

  7. A possible role of alkali metal ions in the synthesis of pure-silica molecular sieves

    OpenAIRE

    Goepper, Michelle; Li, Hong-Xin; Davis, Mark E.

    1992-01-01

    Pure-silica ZSM-12 is synthesized in the presence and absence of alkali metal ions; addition of alkali metal ions at constant hydroxide ion concentration increases the crystallization rate of ZSM-12, and it is suggested that alkali metal ions participate in both the nucleation and crystal growth processes.

  8. Radiation hardening of metals irradiated by heavy ions

    International Nuclear Information System (INIS)

    Didyk, A.Yu.; Skuratov, V.A.; Mikhajlova, N.Yu.; Regel', V.R.

    1988-01-01

    The damage dose dependence in the 10 -4 -10 -2 dpa region of radiation hardening of Al, V, Ni, Cu irradiated by xenon ions with 124 MeV energy is investigated using the microhardness technique and transmission electron microscope. It is shown that the pure metals radiation hardening is stimulated for defects clusters with the typical size less than 5 nm, as in the case of neutron and the light charge ion irradiation

  9. Metal ion effects on enolase activity

    International Nuclear Information System (INIS)

    Lee, M.E.; Nowak, T.

    1986-01-01

    Most metal binding studies with yeast enolase suggest that two metals per monomer are required for catalytic activity. The functions of metal I and metal II have not been unequivocally defined. In a series of kinetic experiments where the concentration of MgII is kept constant at subsaturating levels (1mM), the addition of MnII or of ZnII gives a hyperbolic decrease in activity. The final velocity of these mixed metal systems is the same velocity obtained with either only MnII or ZnII respectively. The concentration of MnII (40 μM) or of Zn (2μM) which gives half maximal effect in the presence of (1mM) MgII is approximately the same as the Km' value for MnII (9μM) or ZnII (3μM) respectively. Direct binding of MnII to enolase in the absence and presence of MgII shows that MnII and MgII compete for the same metal site on enolase. In the presence of 2-phosphoglycerate (2-PGA) and MgII, only a single site is occupied by MnII. Results suggest MnII at site I and MgII at site II. PRR and high resolution 1 H and 31 P NMR studies of enzyme-ligand complexes containing MnII and MgII and MnII are consistent with this model. 31 P measurements allow a measure of the equilibrium constant (0.36) for enolase. Saturation transfer measurements yield net rate constants (k/sub f/ = 0.49s -1 ; k/sub r/ = 1.3s -1 ) for the overall reaction. These values are smaller than k/sub cat/ (38s -1 ) measured under analogous conditions. The cation at site I appears to determine catalytic activity

  10. Crystal structures of Dronpa complexed with quenchable metal ions provide insight into metal biosensor development.

    Science.gov (United States)

    Kim, In Jung; Kim, Sangsoo; Park, Jeahyun; Eom, Intae; Kim, Sunam; Kim, Jin-Hong; Ha, Sung Chul; Kim, Yeon Gil; Hwang, Kwang Yeon; Nam, Ki Hyun

    2016-09-01

    Many fluorescent proteins (FPs) show fluorescence quenching by specific metal ions, which can be applied towards metal biosensor development. In this study, we investigated the significant fluorescence quenching of Dronpa by Co(2+) and Cu(2+) ions. Crystal structures of Co(2+) -, Ni(2+) - and Cu(2+) -bound Dronpa revealed previously unseen, unique, metal-binding sites for fluorescence quenching. These metal ions commonly interact with surface-exposed histidine residues (His194-His210 and His210-His212), and interact indirectly with chromophores. Structural analysis of the Co(2+) - and Cu(2+) - binding sites of Dronpa provides insight into FP-based metal biosensor engineering. © 2016 Federation of European Biochemical Societies.

  11. Functionalization of protein crystals with metal ions, complexes and nanoparticles.

    Science.gov (United States)

    Abe, Satoshi; Maity, Basudev; Ueno, Takafumi

    2018-04-01

    Self-assembled proteins have specific functions in biology. With inspiration provided by natural protein systems, several artificial protein assemblies have been constructed via site-specific mutations or metal coordination, which have important applications in catalysis, material and bio-supramolecular chemistry. Similar to natural protein assemblies, protein crystals have been recognized as protein assemblies formed of densely-packed monomeric proteins. Protein crystals can be functionalized with metal ions, metal complexes or nanoparticles via soaking, co-crystallization, creating new metal binding sites by site-specific mutations. The field of protein crystal engineering with metal coordination is relatively new and has gained considerable attention for developing solid biomaterials as well as structural investigations of enzymatic reactions, growth of nanoparticles and catalysis. This review highlights recent and significant research on functionalization of protein crystals with metal coordination and future prospects. Copyright © 2017 Elsevier Ltd. All rights reserved.

  12. Surface-Modified Membrane as A Separator for Lithium-Ion Polymer Battery

    Directory of Open Access Journals (Sweden)

    Jun Young Kim

    2010-04-01

    Full Text Available This paper describes the fabrication of novel modified polyethylene (PE membranes using plasma technology to create high-performance and cost-effective separator membranes for practical applications in lithium-ion polymer batteries. The modified PE membrane via plasma modification process plays a critical role in improving wettability and electrolyte retention, interfacial adhesion between separators and electrodes, and cycle performance of lithium-ion polymer batteries. This paper suggests that the performance of lithium-ion polymer batteries can be greatly enhanced by the plasma modification of commercial separators with proper functional materials for targeted application.

  13. Focused ion beam lithography for rapid prototyping of metallic films

    Energy Technology Data Exchange (ETDEWEB)

    Osswald, Patrick; Kiermaier, Josef; Becherer, Markus; Schmitt-Landsiedel, Doris [Lehrstuhl fuer Technische Elektronik, TU Muenchen, Munich (Germany)

    2010-07-01

    We present FIB-lithography methods for rapid and cost-effective prototyping of metal structures covering the deep-submicron- to the millimeter-range in a single lithography cycle. Focused ion beam (FIB) systems are widely used in semiconductor industry and research facilities for both analytical testing and prototyping. A typical application is to apply electrical contact to micron-sized sensors/particles by FIB induced metal deposition. However, as for E-beam lithography, patterning times for large area bonding pads are unacceptably long, resulting in cost-intensive prototyping. In this work, we optimized FIB lithography processing for negative and positive imaging mode to form metallic structures for large-areas down do the sub-100 nm range. For negative lithography features are defined by implanting Ga{sup +}-ions into a commercial photo resist, without affecting the underlying structures by impinging ions. The structures are highly suitable for following lift-off processing due to the undercut of the resist.Metallic feature size of down to 150 nm are achievable. For positive lithography a PMMA resist is exposed in FIB irradiation. Due to the very low dose (3.10{sup 12} ions/cm{sup 2}) the writing time for an e.g. 100 {mu}m x 100 {mu}m square is approx. 15 seconds. The developed resist is used for subsequent wet chemical etching, obtaining a 100 nm resolution in metal layers.

  14. Metal oxide collectors for storing matter technique applied in secondary ion mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Miśnik, Maciej [Institute of Tele and Radio Technology, ul. Ratuszowa 11, 03-450 Warszawa (Poland); Gdańsk University of Technology (Poland); Konarski, Piotr [Institute of Tele and Radio Technology, ul. Ratuszowa 11, 03-450 Warszawa (Poland); Zawada, Aleksander [Institute of Tele and Radio Technology, ul. Ratuszowa 11, 03-450 Warszawa (Poland); Military University of Technology, Warszawa (Poland)

    2016-03-15

    We present results of the use of metal and metal oxide substrates that serve as collectors in ‘storing matter’, the quantitative technique of secondary ion mass spectrometry (SIMS). This technique allows separating the two base processes of secondary ion formation in SIMS. Namely, the process of ion sputtering is separated from the process of ionisation. The technique allows sputtering of the analysed sample and storing the sputtered material, with sub-monolayer coverage, onto a collector surface. Such deposits can be then analysed by SIMS, and as a result, the so called ‘matrix effects’ are significantly reduced. We perform deposition of the sputtered material onto Ti and Cu substrates and also onto metal oxide substrates as molybdenum, titanium, tin and indium oxides. The process of sputtering is carried within the same vacuum chamber where the SIMS analysis of the collected material is performed. For sputtering and SIMS analysis of the deposited material we use 5 keV Ar{sup +} beam of 500 nA. The presented results are obtained with the use of stationary collectors. Here we present a case study of chromium. The obtained results show that the molybdenum and titanium oxide substrates used as collectors increase useful yield by two orders, with respect to such pure elemental collectors as Cu and Ti. Here we define useful yield as a ratio of the number of detected secondary ions during SIMS analysis and the number of atoms sputtered during the deposition process.

  15. Smart responsive microcapsules capable of recognizing heavy metal ions.

    Science.gov (United States)

    Pi, Shuo-Wei; Ju, Xiao-Jie; Wu, Han-Guang; Xie, Rui; Chu, Liang-Yin

    2010-09-15

    Smart responsive microcapsules capable of recognizing heavy metal ions are successfully prepared with oil-in-water-in-oil double emulsions as templates for polymerization in this study. The microcapsules are featured with thin poly(N-isopropylacrylamide-co-benzo-18-crown-6-acrylamide) (P(NIPAM-co-BCAm)) membranes, and they can selectively recognize special heavy metal ions such as barium(II) or lead(II) ions very well due to the "host-guest" complexation between the BCAm receptors and barium(II) or lead(II) ions. The stable BCAm/Ba(2+) or BCAm/Pb(2+) complexes in the P(NIPAM-co-BCAm) membrane cause a positive shift of the volume phase transition temperature of the crosslinked P(NIPAM-co-BCAm) hydrogel to a higher temperature, and the repulsion among the charged BCAm/Ba(2+) or BCAm/Pb(2+) complexes and the osmotic pressure within the P(NIPAM-co-BCAm) membranes result in the swelling of microcapsules. Induced by recognizing barium(II) or lead(II) ions, the prepared microcapsules with P(NIPAM-co-BCAm) membranes exhibit isothermal and significant swelling not only in outer and inner diameters but also in the membrane thickness. The proposed microcapsules in this study are highly attractive for developing smart sensors and/or carriers for detection and/or elimination of heavy metal ions. Copyright 2010 Elsevier Inc. All rights reserved.

  16. Albumin as marker for susceptibility to metal ions in metal-on-metal hip prosthesis patients.

    Science.gov (United States)

    Facchin, F; Catalani, S; Bianconi, E; Pasquale, D De; Stea, S; Toni, A; Canaider, S; Beraudi, A

    2017-04-01

    Metal-on-metal (MoM) hip prostheses are known to release chromium and cobalt (Co), which negatively affect the health status, leading to prosthesis explant. Albumin (ALB) is the main serum protein-binding divalent transition metals. Its binding capacity can be affected by gene mutations or modification of the protein N-terminal region, giving the ischaemia-modified albumin (IMA). This study evaluated ALB, at gene and protein level, as marker of individual susceptibility to Co in MoM patients, to understand whether it could be responsible for the different management of this ion. Co was measured in whole blood, serum and urine of 40 MoM patients. A mutational screening of ALB was performed to detect links between mutations and metal binding. Finally, serum concentration of total ALB and IMA were measured. Serum total ALB concentration was in the normal range for all patients. None of the subjects presented mutations in the investigated gene. Whole blood, serum and urine Co did not correlate with serum total ALB or IMA, although IMA was above the normal limit in most subjects. The individual susceptibility is very important for patients' health status. Despite the limited results of this study, we provide indications on possible future investigations on the toxicological response to Co.

  17. Adsorption of Metallic Ions onto Chitosan : Equilibrium and Kinetic Studies

    OpenAIRE

    Benavente, Martha

    2008-01-01

    Equilibrium isotherms and the adsorption kinetics of heavy metals onto chitosan were studied experimentally. Chitosan, a biopolymer produced from crustacean shells, has applications in various areas, particularly in drinking water and wastewater treatment due to its ability to remove metallic ions from solutions. The adsorption capacity of chitosan depends on a number of parameters: deacetylation degree, molecular weight, particle size and crystallinity. The purpose of this work was to study ...

  18. Metal ion binding to iron oxides

    NARCIS (Netherlands)

    Hiemstra, T.; Riemsdijk, van W.H.; Benedetti, M.F.; Ponthieu, M.

    2006-01-01

    The biogeochemistry of trace elements (TE) is largely dependent upon their interaction with heterogeneous ligands including metal oxides and hydrous oxides of iron. The modeling of TE interactions with iron oxides has been pursued using a variety of chemical models. The objective of this work is to

  19. DETERMINATION OF METAL IONS RELEASED BY STAINLESS ...

    African Journals Online (AJOL)

    Preferred Customer

    Also taking into account the fact that, in body conditions implant corrosion products are disseminated and eventually eliminated. The result that SS arch bar used in orthodontic appliances corrode in bio-fluids over an extended time interval is of great clinical significance in evaluating their bio-compatibility, the levels of metal.

  20. Hydrometallurgical recovery of metal values from sulfuric acid leaching liquor of spent lithium-ion batteries.

    Science.gov (United States)

    Chen, Xiangping; Chen, Yongbin; Zhou, Tao; Liu, Depei; Hu, Hang; Fan, Shaoyun

    2015-04-01

    Environmentally hazardous substances contained in spent Li-ion batteries, such as heavy metals and nocuous organics, will pose a threat to the environment and human health. On the other hand, the sustainable recycling of spent lithium-ion batteries may bring about environmental and economic benefits. In this study, a hydrometallurgical process was adopted for the comprehensive recovery of nickel, manganese, cobalt and lithium from sulfuric acid leaching liquor from waste cathode materials of spent lithium-ion batteries. First, nickel ions were selectively precipitated and recovered using dimethylglyoxime reagent. Recycled dimethylglyoxime could be re-used as precipitant for nickel and revealed similar precipitation performance compared with fresh dimethylglyoxime. Then the separation of manganese and cobalt was conducted by solvent extraction method using cobalt loaded D2EHPA. And McCabe-Thiele isotherm was employed for the prediction of the degree of separation and the number of extraction stages needed at specific experimental conditions. Finally, cobalt and lithium were sequentially precipitated and recovered as CoC2O4 ⋅ 2H2O and Li2CO3 using ammonium oxalate solution and saturated sodium carbonate solution, respectively. Recovery efficiencies could be attained as follows: 98.7% for Ni; 97.1% for Mn, 98.2% for Co and 81.0% for Li under optimized experimental conditions. This hydrometallurgical process may promise a candidate for the effective separation and recovery of metal values from the sulfuric acid leaching liquor. Copyright © 2015 Elsevier Ltd. All rights reserved.

  1. Ion exchange of alkaline metals on the thin-layer zinc ferrocyanide

    International Nuclear Information System (INIS)

    Betenekov, N.D.; Buklanov, G.V.; Ipatova, E.G.; Korotkin, Yu.S.

    1991-01-01

    Basic regularities of interphase distribution in the system of thin-layer sorbent on the basis of mixed zinc ferrocyanide (FZ)-alkaline metal solution (Na, K, Rb, Cs, Fr) in the column chromatography made are studied. It is established that interphase distribution of microgram amounts of alkaline metals in the systems thin-layer FZ-NH 4 NO 3 electrolyte solutions is of ion-exchange character and subjected to of law effective mass. It is shown that FZ thin-layer material is applicable for effective chromatographic separation of alkaline metal trace amounts. An approach to the choice of a conditions of separate elution of Na, K, Rb, Cs, Fr in the column chromatography mode

  2. Plasma processes in the preparation of lithium-ion battery electrodes and separators

    Science.gov (United States)

    Nava-Avendaño, J.; Veilleux, J.

    2017-04-01

    Lithium-ion batteries (LIBs) are the energy storage devices that dominate the portable electronic market. They are now also considered and used for electric vehicles and are foreseen to enable the smart grid. Preparing batteries with high energy and power densities, elevated cycleability and improved safety could be achieved by controlling the microstructure of the electrode materials and the interaction they have with the electrolyte over the working potential window. Selecting appropriate precursors, reducing the preparation steps and selecting more efficient synthesis methods could also significantly reduce the costs of LIB components. Implementing plasma technologies can represent a high capital investment, but the versatility of the technologies allows the preparation of powdered nanoparticles with different morphologies, as well as with carbon and metal oxide coatings. Plasma technologies can also enable the preparation of binder-free thin films and coatings for LIB electrodes, and the treatment of polymeric membranes to be used as separators. This review paper aims at highlighting the different thermal and non-thermal plasma technologies recently used to synthesize coated and non-coated active materials for LIB cathodes and anodes, and to modify the surface of separators.

  3. Spin-Charge Separation in Finite Length Metallic Carbon Nanotubes

    KAUST Repository

    Zhang, Yongyou

    2017-10-17

    Using time-dependent density functional theory, we study the optical excitations in finite length carbon nanotubes. Evidence of spin-charge separation is given in the spacetime domain. We demonstrate that the charge density wave is due to collective excitations of electron singlets, while the accompanying spin density wave is due to those of electron triplets. The Tomonaga–Luttinger liquid parameter and density–density interaction are extrapolated from the first-principles excitation energies. We show that the density–density interaction increases with the length of the nanotube. The singlet and triplet excitation energies, on the other hand, decrease for increasing length of the nanotube. Their ratio is used to establish a first-principles approach for deriving the Tomonaga–Luttinger parameter (in excellent agreement with experimental data). Time evolution analysis of the charge and spin line densities evidences that the charge and spin density waves are elementary excitations of metallic carbon nanotubes. Their dynamics show no dependence on each other.

  4. Sorption of heavy metal ions on new metal-ligand complexes chemically derived from Lycopodium clavatum

    Energy Technology Data Exchange (ETDEWEB)

    Pehlivan, E.; Ersoz, M.; Yildiz, S. [Univ. of Selcuk, Konya (Turkey); Duncan, H.J. [Univ. of Glasgow, Scotland (United Kingdom)

    1994-08-01

    Sorption of heavy metal ions from aqueous solution has been investigated as a function of pH using a novel exchanger system whereby Lycopodium clavatum is functionalized with carboxylate and glyoxime metal-ligand complexes. The new ligand exchangers were prepared using a reaction of diaminosporopollenin with various metal-ligand complexes of glyoxime and monocarboxylic acid. The sorptive behavior of these metal-ligand exchangers and the possibilities to remove and to recover selectively heavy metal cations using these systems are discussed on the basis of their chemical natures and their complexing properties.

  5. Immobilization of Metal Hexacyanoferrate Ion-Exchangers for the Synthesis of Metal Ion Sorbents—A Mini-Review

    Directory of Open Access Journals (Sweden)

    Thierry Vincent

    2015-11-01

    Full Text Available Metal hexacyanoferrates are very efficient sorbents for the recovery of alkali and base metal ions (including radionuclides such as Cs. Generally produced by the direct reaction of metal salts with potassium hexacyanoferrate (the precursors, they are characterized by ion-exchange and structural properties that make then particularly selective for Cs(I, Rb(I and Tl(I recovery (based on their hydrated ionic radius consistent with the size of the ion-exchanger cage, though they can bind also base metals. The major drawback of these materials is associated to their nanometer or micrometer size that makes them difficult to recover in large-size continuous systems. For this reason many techniques have been designed for immobilizing these ion-exchangers in suitable matrices that can be organic (mainly polymers and biopolymers or inorganic (mineral supports, carbon-based matrices. This immobilization may proceed by in situ synthesis or by entrapment/encapsulation. This mini-review reports some examples of hybrid materials synthesized for the immobilization of metal hexacyanoferrate, the different conditionings of these composite materials and, briefly, the parameters to take into account for their optimal design and facilitated use.

  6. Breast milk metal ion levels in a young and active patient with a metal-on-metal hip prosthesis.

    Science.gov (United States)

    Nelis, Raymond; de Waal Malefijt, Jan; Gosens, Taco

    2013-01-01

    Metal-on-metal resurfacing arthroplasty of the hip has been used increasingly over the last 10 years in younger active patients. The dissolution of the metal wear particles results in measurable increases in cobalt and chromium ions in the serum and urine of patients with a metal-on-metal bearing. We measured the cobalt, chromium, and molybdenum ion levels in urine; serum; and breast milk in a young and active patient with a metal-on-metal hip prosthesis after a pathologic fracture of the femoral neck. Metal-on-metal hip prosthesis leads to increasing levels of molybdenum in breast milk in the short-term follow-up. There are no increasing levels of chromium and cobalt ions in breast milk. Besides the already known elevated concentrations in serum of chromium and cobalt after implantation of a metal-on-metal hip prosthesis, we found no increasing levels of chromium and cobalt in urine. Copyright © 2013 Elsevier Inc. All rights reserved.

  7. Separation of Ra/Ca by ion exchange

    International Nuclear Information System (INIS)

    Iturbe, J.L.; Jimenez R, M.; Flores M, J.

    1991-04-01

    The radium and the calcium belong to the same group in the periodic classification and as consequence both they present very similar chemical properties, that makes difficult its separation. Both elements are also frequently associate in the nature, the calcium is very abundant, the radium is not it and for that reason it is indispensable its separation to analyze to this last one. The alpha spectroscopy is very appropriate to analyze to the 226 Ra, however to achieve a good resolution of the spectra, the samples should contain small quantities of calcium. The purposes of this work were to know the chromatographic behavior of the alkaline-earthy cations: calcium, barium and radium and to apply these knowledge to the separation of the 226 Ra and its analysis by means of alpha spectroscopy. (Author)

  8. Adsorption of heavy metals ions on portulaca oleracea plants

    International Nuclear Information System (INIS)

    Naqvi, R.R.

    2005-01-01

    The aim of this study is to report the ability of portulaca oleracea (Fershi in Urdu) biomass grown in uncontaminated soils to adsorb or uptake lead, cadmium, arsenic, cobalt and copper from aqueous solutions. In order to help understand the metal binding mechanism, laboratory experiments performance to determine optimal binding, and binding capacity for each of the above mentioned metals. These experiments were carried out for the mass of crushed portulaca stems. Portulaca is a plant that grows abundantly in temperature climate in the area of Quetta Balochistan. It has reddish stem and thick succulent leaves. This plant has been found to be good adsorbent for heavy metals ions. (author)

  9. Radio-frequency ion deflector for mass separation

    Energy Technology Data Exchange (ETDEWEB)

    Schlösser, Magnus, E-mail: magnus.schloesser@googlemail.com; Rudnev, Vitaly; Ureña, Ángel González, E-mail: laseres@pluri.ucm.es [Unidad de Láseres y Haces Moleculares, Instituto Plurisdisciplinar, Universidad Complutense de Madrid, Madrid 28040 (Spain)

    2015-10-15

    Electrostatic cylindrical deflectors act as energy analyzer for ion beams. In this article, we present that by imposing of a radio-frequency modulation on the deflecting electric field, the ion transmission becomes mass dependent. By the choice of the appropriate frequency, amplitude, and phase, the deflector can be used as mass filter. The basic concept of the new instrument as well as simple mathematic relations are described. These calculations and further numerical simulations show that a mass sensitivity is achievable. Furthermore, we demonstrate the proof-of-principle in experimental measurements, compare the results to those of from a 1 m linear time-of-flight spectrometer, and comment on the mass resolution of the method. Finally, some potential applications are indicated.

  10. Method of separating radioactive nuclides from ion exchange resins

    International Nuclear Information System (INIS)

    Suzuki, Kazunori; Saikoku, Masami; Taneta, Daisuke; Yagi, Takuro.

    1987-01-01

    Purpose: To enable to safely process radioactive nuclides from spent ion exchange resins by using existent processing facilities. Method: Ion exchange resins in aqueous medium are at first placed to the ultrasonic wave irradiation site and put into such a state where clads and resins are easily separatable from each other by weakening the bonding force between them. Since the clads are magnetic material such as Fe 3 O 4 or NiFe 2 O 4 , the clads can be collected in the direction of the magnetic force by exerting the magnetic field simultaneously. The collected clads are transported by means of the aqueous medium to a collecting tank by removing the effect of magnetic field, for example, by interrupting the current supply to the electromagnet. Finally, they were subjected to stabilization and fixation into inorganic hardening agent such as cement hardener. Thus, processions can be made safely by using existent facilities. (Takahashi, M.)

  11. Water-soluble metal-binding polymers with ultrafiltration: A technology for the removal, concentration, and recovery of metal ions from aqueous streams

    International Nuclear Information System (INIS)

    Smith, B.F.; Robison, T.W.; Jarvinen, G.D.

    1997-01-01

    The use of water-soluble metal-binding polymers coupled with ultrafiltration (UF) is a technology under development to selectively concentrate and recover valuable or regulated metal-ions from dilute process or waste waters. The polymers have a sufficiently large molecular size that they can be separated and concentrated using commercially available UF technology. The polymers can then be reused by changing the solution conditions to release the metal-ions, which are recovered in a concentrated form for recycle or disposal. Pilot-scale demonstrations have been completed for a variety of waste streams containing low concentrations of metal ions including electroplating wastes (zinc and nickel) and nuclear waste streams (plutonium and americium). Many other potential commercial applications exist including remediation of contaminated solids. An overview of both the pilot-scale demonstrated applications and small scale testing of this technology are presented

  12. Water-soluble metal-binding polymers with ultrafiltration: A technology for the removal, concentration, and recovery of metal ions from aqueous streams

    Energy Technology Data Exchange (ETDEWEB)

    Smith, B.F.; Robison, T.W.; Jarvinen, G.D.

    1997-12-31

    The use of water-soluble metal-binding polymers coupled with ultrafiltration (UF) is a technology under development to selectively concentrate and recover valuable or regulated metal-ions from dilute process or waste waters. The polymers have a sufficiently large molecular size that they can be separated and concentrated using commercially available UF technology. The polymers can then be reused by changing the solution conditions to release the metal-ions, which are recovered in a concentrated form for recycle or disposal. Pilot-scale demonstrations have been completed for a variety of waste streams containing low concentrations of metal ions including electroplating wastes (zinc and nickel) and nuclear waste streams (plutonium and americium). Many other potential commercial applications exist including remediation of contaminated solids. An overview of both the pilot-scale demonstrated applications and small scale testing of this technology are presented.

  13. Study of ion separation through solid-supported liquid membrane

    International Nuclear Information System (INIS)

    Kang, Young Ho; Kim, Jung Do; Kim, Kyoung Ho

    1990-01-01

    The membranes used in this study consist of a microporous polymeric support with the solvent contraining alamine 336, Tri-N-Octyl phosphine oxide, Tri-N-butyl phosphate, Di-(2-ethylhexyl) phosphoric acid as a carrier within the pores by the capillary forces. When this liquid membrane is interposed between aqueous feed and product solutions, the carrier serving as a complexing agent, can pick up the uranium ions on the feed side of the membrane and carry them across the membrane by diffusion. In this study, the uranium flux through the solid-supported liquid membrane was analyzed as a function of carrier concentration and acidity of the feed solution for the carrier species. Also, the Gel-liquid extraction of uranium ions from aqueous solution was performed. The adsorbents were prepared by casting the polymer solution composed of polyvinyl chloride, TOPO, and additions. The extraction of uranyl nitrate ions has been investigated as a function of TOPO/PVC ratio, evaporation time, and the stability. The results show that is maybe possible to develop an alternative uranium purification process. (author)

  14. Chromium and cobalt ion concentrations in blood and serum following various types of metal-on-metal hip arthroplasties

    DEFF Research Database (Denmark)

    Jantzen, Christopher; Jørgensen, Henrik L; Duus, Benn R

    2013-01-01

    Widely different metal ion concentrations in blood and serum have been reported with metal-on-metal (MoM) implants. We reviewed the literature on blood and serum ion concentrations of chromium (Cr) and cobalt (Co) following various MoM hip arthroplasties.......Widely different metal ion concentrations in blood and serum have been reported with metal-on-metal (MoM) implants. We reviewed the literature on blood and serum ion concentrations of chromium (Cr) and cobalt (Co) following various MoM hip arthroplasties....

  15. Neutralization by metal ions of the toxicity of sodium selenide.

    Directory of Open Access Journals (Sweden)

    Marc Dauplais

    Full Text Available Inert metal-selenide colloids are found in animals. They are believed to afford cross-protection against the toxicities of both metals and selenocompounds. Here, the toxicities of metal salt and sodium selenide mixtures were systematically studied using the death rate of Saccharomyces cerevisiae cells as an indicator. In parallel, the abilities of these mixtures to produce colloids were assessed. Studied metal cations could be classified in three groups: (i metal ions that protect cells against selenium toxicity and form insoluble colloids with selenide (Ag⁺, Cd²⁺, Cu²⁺, Hg²⁺, Pb²⁺ and Zn²⁺, (ii metal ions which protect cells by producing insoluble metal-selenide complexes and by catalyzing hydrogen selenide oxidation in the presence of dioxygen (Co²⁺ and Ni²⁺ and, finally, (iii metal ions which do not afford protection and do not interact (Ca²⁺, Mg²⁺, Mn²⁺ or weakly interact (Fe²⁺ with selenide under the assayed conditions. When occurring, the insoluble complexes formed from divalent metal ions and selenide contained equimolar amounts of metal and selenium atoms. With the monovalent silver ion, the complex contained two silver atoms per selenium atom. Next, because selenides are compounds prone to oxidation, the stabilities of the above colloids were evaluated under oxidizing conditions. 5,5'-dithiobis-(2-nitrobenzoic acid (DTNB, the reduction of which can be optically followed, was used to promote selenide oxidation. Complexes with cadmium, copper, lead, mercury or silver resisted dissolution by DTNB treatment over several hours. With nickel and cobalt, partial oxidation by DTNB occurred. On the other hand, when starting from ZnSe or FeSe complexes, full decompositions were obtained within a few tens of minutes. The above properties possibly explain why ZnSe and FeSe nanoparticles were not detected in animals exposed to selenocompounds.

  16. CONTINUOUS CHELATION-EXTRACTION PROCESS FOR THE SEPARATION AND PURIFICATION OF METALS

    Science.gov (United States)

    Thomas, J.R.; Hicks, T.E.; Rubin, B.; Crandall, H.W.

    1959-12-01

    A continuous process is presented for separating metal values and groups of metal values from each other. A complex mixture. e.g., neutron-irradiated uranium, can be resolved into component parts. In the present process the values are dissolved in an acidic solution and adjusted to the proper oxidation state. Thenceforth the solution is contacted with an extractant phase comprising a fluorinated beta -diketone in an organic solvent under centain pH conditions whereupon plutonium and zirconium are extracted. Plutonium is extracted from the foregoing extract with reducing aqueous solutions or under specified acidic conditions and can be recovered from the aqueous solution. Zirconium is then removed with an oxalic acid aqueous phase. The uranium is recovered from the residual original solution using hexone and hexone-diketone extractants leaving residual fission products in the original solution. The uranium is extracted from the hexone solution with dilute nitric acid. Improved separations and purifications are achieved using recycled scrub solutions and the "self-salting" effect of uranyl ions.

  17. Effects of Alkali-Metal Ions and Counter Ions in Sn-Beta-Catalyzed Carbohydrate Conversion.

    Science.gov (United States)

    Elliot, Samuel G; Tolborg, Søren; Madsen, Robert; Taarning, Esben; Meier, Sebastian

    2018-02-26

    Alkali-metal ions have recently been shown to strongly influence the catalytic behavior of stannosilicates in the conversion of carbohydrates. An effect of having alkali-metal ions present is a pronounced increase in selectivity towards methyl lactate. Mechanistic details of this effect have remained obscure and are herein addressed experimentally through kinetic experiments and isotope tracking. The presence of alkali-metal ions has a differential effect in competing reaction pathways and promotes the rate of carbon-carbon bond breakage of carbohydrate substrates, but decreases the rates of competing dehydration pathways. Further addition of alkali-metal ions inhibits the activity of Sn-Beta in all major reaction pathways. The alkali-metal effects on product distribution and on the rate of product formation are similar, thus pointing to a kinetic reaction control and to irreversible reaction steps in the main pathways. Additionally, an effect of the accompanying basic anions is shown, supposedly facilitating the cation exchange and eliciting a different concentration-dependent effect to that of neutral alkali-metal salts. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Host Materials for Transition-Metal Ions

    Science.gov (United States)

    1989-09-01

    Phys. 5cr. 25 (1982), 924. J4. L. DiSiplo, E. Tondello, G. De~ichelis, and L. Oleari , Slater-Condon Parameters for Atoms and Ions of the Second...Bnm* Frequently, the point-charge crystal-field components, Anm, indicate the correct phase relations and are used to determine the phases reported in...745. 5. W. L. Bond, Measurement of the Refractive Indices of Several Crystals, J. Appl. Phys. 36 (1965), 1674. 6. G. Burns, E. A. Geiss, B. A

  19. Effect of sulphate and chloride ions on the solvent extraction of some metal ions with liquid cation exchangers

    International Nuclear Information System (INIS)

    Shibata, Junji; Nishimura, Sanji

    1977-01-01

    The extraction of the metal ions from sulphate and chloride solutions with Versatic Acid 911 and di(2-ethyl hexyl) phosphoric acid in benzene was investigated in order to clarify the effect of sulphate and chloride ions on the extraction. Sulphate and chloride ions are not extracted into the organic phase, and they affect metal extraction only by forming the complexes with metal ions in the aqueous phase. The extent of the effect on metal extraction is determined by the kind of metal ions and anionic ligands, and the concentration of ligand ions. Therefore, the difference in extraction behaviour may be explained by the complexing ability of the various anionic ligands present in the aqueous phase. Formation constants of the complexes between metal ions and anionic ligands were computed from these distribution data. (auth.)

  20. Interaction of Hydroxyproline with Bivalent Metal Ions in Chemical ...

    African Journals Online (AJOL)

    Arecent technique involving the use of paper electrophoresis is described for the study of equilibria in binary complex systems in solution. The stability constants of the ML and ML2 complex species of some metal ions, namely beryllium(II) and cobalt(II), with hydroxyproline were determined in 0.1 mol L–1 perchloric acid ...

  1. Speciation and stability of methylene blue-metal-thiocyanate ion ...

    African Journals Online (AJOL)

    The relative stabilities indicate that cobalt is preferred to other two metals in the speciation of ternary complexes comparable with similar complexes in biosystems. This study also provides a method for the spectrophotometric determination of Co(II) and Zn(II) ions at nanogram levels at 25 oC and an ionic strength of 0.15 M.

  2. Dimeric Complexes of Tryptophan with M2+ Metal Ions

    NARCIS (Netherlands)

    Dunbar, R. C.; Steill, J. D.; Polfer, N. C.; Oomens, J.

    2009-01-01

    IRMPD spectroscopy using the FELIX free electron laser and a Fourier transform ICR mass spectrometer was used to characterize the structures of electrosprayed dimer complexes M(2+)Trp(2) of tryptophan with a series of eight doubly charged metal ions, including alkaline earths Ca, Sr, and Ba, and

  3. Synthesis, photophysical and metal ion signalling behaviour of mono

    Indian Academy of Sciences (India)

    Unknown

    Fluorescence decay behaviour of the systems suggests a through-space nature of PET. The systems exhi- bit off–on fluorescence signalling in the aprotic media in the presence of several metal ions, some of which are well known for their fluorescence quenching abilities. Diazacrown derivative, II, appears to be a somewhat ...

  4. Utilization of Plant Refuses as Component of Heavy Metal Ion ...

    African Journals Online (AJOL)

    The ability of the fabricated sensors to detect the presence of heavy metals was analyzed using electrochemical methods like cyclic voltammetry and differential pulse anodic stripping voltammetry. Results showed that the fabricated electrode were able to detect the presence of mercury and lead ions in aqueous solutions ...

  5. Removal of metal ions using dead-end filtration

    African Journals Online (AJOL)

    2005-07-03

    Jul 3, 2005 ... Surfactants due to their high selectivity properties have been used in enhancing membrane filtration for the removal of metal ions in aqueous solutions. Natural surfactants are preferred to synthetic surfactants because the synthetic surfactants have the disadvantage of introducing secondary pollutants into ...

  6. Equilibrium and kinetics studies of metal ion adsorption on dyed ...

    African Journals Online (AJOL)

    Batch equilibration studies were conducted to determine the nature of adsorption of Zn (II) and Cu (II) onto dyed coconut pollens. The nature of adsorption of metal ions was explained using the Langmuir equation. The calculated values of equilibrium parameter indicated favourable adsorption by the adsorbents. Also the ...

  7. Effect of metal ion doping on the photocatalytic activity of ...

    Indian Academy of Sciences (India)

    The activity can be enhanced by the increasing of concentration of the doped metal ions. TiAlPO-5 (4, 8, 12 atom % of Ti) showed the highest photocatalytic activity among all the compounds and its activity was compared to that of Degussa P25 (TiO2). The activity of photocatalysts was correlated with the diffuse reflectance ...

  8. Equilibrium and kinetics studies of metal ion adsorption on dyed ...

    African Journals Online (AJOL)

    GREGO

    2007-04-02

    Apr 2, 2007 ... Batch equilibration studies were conducted to determine the nature of adsorption of Zn (II) and Cu (II) onto dyed coconut pollens. The nature of adsorption of metal ions was explained using the Langmuir equation. The calculated values of equilibrium parameter indicated favourable adsorption by the.

  9. Broad-beam, high current, metal ion implantation facility

    International Nuclear Information System (INIS)

    Brown, I.G.; Dickinson, M.R.; Galvin, J.E.; Godechot, X.; MacGill, R.A.

    1990-07-01

    We have developed a high current metal ion implantation facility with which high current beams of virtually all the solid metals of the Periodic Table can be produced. The facility makes use of a metal vapor vacuum arc ion source which is operated in a pulsed mode, with pulse width 0.25 ms and repetition rate up to 100 pps. Beam extraction voltage is up to 100 kV, corresponding to an ion energy of up to several hundred keV because of the ion charge state multiplicity; beam current is up to several Amperes peak and around 10 mA time averaged delivered onto target. Implantation is done in a broad-beam mode, with a direct line-of-sight from ion source to target. Here we describe the facility and some of the implants that have been carried out using it, including the 'seeding' of silicon wafers prior to CVD with titanium, palladium or tungsten, the formation of buried iridium silicide layers, and actinide (uranium and thorium) doping of III-V compounds. 16 refs., 6 figs

  10. Do soft drinks affect metal ions release from orthodontic appliances?

    Science.gov (United States)

    Mikulewicz, Marcin; Wołowiec, Paulina; Loster, Bartłomiej W; Chojnacka, Katarzyna

    2015-01-01

    The effect of orange juice and Coca Cola(®) on the release of metal ions from fixed orthodontic appliances. A continuous flow system designed for in vitro testing of orthodontic appliances was used. Orange juice/Coca Cola(®) was flowing through the system alternately with artificial saliva for 5.5 and 18.5h, respectively. The collected samples underwent a multielemental ICP-OES analysis in order to determine the metal ions release pattern in time. The total mass of ions released from the appliance into orange juice and Coca Cola(®) (respectively) during the experiment was calculated (μg): Ni (15.33; 37.75), Cr (3.604; 1.052), Fe (48.42; ≥ 156.1), Cu (57.87, 32.91), Mn (9.164; 41.16), Mo (9.999; 30.12), and Cd (0.5967; 2.173). It was found that orange juice did not intensify the release of metal ions from orthodontic appliances, whereas Coca Cola(®) caused increased release of Ni ions. Copyright © 2015 Elsevier GmbH. All rights reserved.

  11. studies on the use of organic and inorganic ion exchangers for separation of indium(III) from cadmium(II) using analytical methods

    International Nuclear Information System (INIS)

    Mohamed, A.A.E.

    2011-01-01

    Organic and inorganic ion exchangers have many applications not only in the industrial, environmental and the nuclear fields but also in the separation of metal ions. This may be returned to its high measured capacity, high selectivity for some metal ions, low solubility, high chemical radiation stability and easy to use.Indium and cadmium are produced from cyclotron target where the solvent extraction represents an ordinary method for separation of indium and cadmium from its target. In the present work, More than chromatographic columns were successfully used for the separation and recovery of indium(III) and cadmium(II) ions from di-component system in aqueous solution using organic and inorganic ion exchangers. The work was carried out in three main parts;1- In the first part, the commercial resin (Dowex50w-x8) was used for the separation of indium from cadmium. The effect of pH, the weight of resin, and equilibrium time on the sorption process of both metal ions were determined. It was found that the adsorption percentage was more than 99% at pH 4 (as optimum pH value) using batch experiment. The results show that indium was first extracted while cadmium is slightly extracted at this pH value. The recovery of indium and cadmium is about 98% using hydrochloric acid as best eluent. The ion exchange/complexing properties of Dowex50w-x8 resin containing various substituted groups towards indium and cadmium cations were investigated.2- In the second part, Zn(II)polymethacrylates, and poly (acrylamide-acrylic acid), as synthetic organic ion exchangers were prepared by gamma irradiation polymerization technique of the corresponding monomer at 30 kGy. The obtained organic resins were mixed with indium ions to determine its capacity in aqueous solutions using batch experiment.

  12. Selective chelation-supercritical fluid extraction of metal ions from waste materials

    International Nuclear Information System (INIS)

    Wai, C.N.; Laintz, K.E.; Yonker, C.R.

    1993-01-01

    The removal of toxic organics, metals, and radioisotopes from solids or liquids is a major concern in the treatment of industrial and nuclear wastes. For this reason, developing methods for selective separation of toxic metals and radioactive materials from solutions of complex matrix is an important problem in environmental research. Recent developments indicate supercritical fluids are good solvents for organic compounds. Many gases become supercritical fluids under moderate temperatures and pressures. For example, the critical temperature and pressure of carbon dioxide are 31 degrees C and 73 atm, respectively. The high diffusivity, low viscosity, and T-P dependence of solvent strength are some attractive properties of supercritical fluid extraction (SFE). Since CO 2 offers the additional benefits of stability and non-toxicity, the SFE technique avoids generation of organic liquid waste and exposure of personnel to toxic solvents. While direct extraction of metal ions by supercritical fluids is highly inefficient, these ions when complexed with organic ligands become quite soluble in supercritical fluids. Specific ligands can be used to achieve selective extraction of metal ions in this process. After SFE, the fluid phase can be depressurized for precipitation of the metal chelates and recycled. The ligand can also be regenerated for repeated use. The success of this selective chelation-supercritical fluid extraction (SC-SFE) process depends on a number of factors including the efficiencies of the selective chelating agents, solubilities of metal chelates in supercritical fluids, rate of extraction, ease of regeneration of the ligands, etc. In this report, the authors present recent results on the studies of the solubilities of metal chelates in supercritical CO 2 , experimental ions from aqueous solution, and the development of selective chelating agents (ionizable crown ethers) for the extraction of lanthanides and actinides

  13. Use of weak ion association in the separation of inorganic anions by ...

    African Journals Online (AJOL)

    In this work weak ion association was used to effect selectivity and detection of inorganic anions with environmental or health significance by capillary electropheresis, CE. Tetrabutylammonium ion was used as a pairing anion to separate mixtures containing closely or co-migrating inorganic anions at pHs 3.8 and pH 7.

  14. First measurement of radioisotopes by collinear laser spectroscopy at an ion-guide separator

    NARCIS (Netherlands)

    Cooke, JL; Billowes, J; Campbell, P; Cochrane, ECA; Cooper, TG; Dendooven, P; Evans, DE; Griffith, JAR; Grant, IS; Honkanen, A; Huhta, M; Levins, JMG; Oinonen, M; Pearson, MR; Penttila, H; Persson, B.L.; Richardson, DS; Tungate, G; Wheeler, PD; Zybert, L; Aysto, J

    1997-01-01

    The first successful application of an ion-guide separator (IGISOL) for collinear laser spectroscopy of radioisotopes has achieved an efficiency comparable with the best obtained with catcher-ionizer facilities. The ion beam energy spread was determined to be less than 6 eV, allowing laser

  15. Cementation of silver ions on metallic copper

    International Nuclear Information System (INIS)

    Jaskula, M.

    2009-01-01

    The silver cementation on metallic copper was investigated in the presence or absence of oxygen. The influence of sulphuric acid and copper sulphate concentration on the silver cement morphology was studied in details, and results were linked with the previously determined kinetics data of the process. The morpgology of silver depopsit was found to be independent of the prosence of oxygen in the system in as well as the sulphuric acide concentration. Contrary, the concentration of copper sulphate strongly influenced the morphology of silver deposite. Two-stage mechanism of cementation was proposed. (authors).

  16. Very broad beam metal ion source for large area ion implantation application

    International Nuclear Information System (INIS)

    Brown, I.; Anders, S.; Dickinson, M.R.; MacGill, R.A.; Yao, X.

    1993-01-01

    The authors have made and operated a very broad beam version of vacuum arc ion source and used it to carry out high energy metal ion implantation of a particularly large substrate. A multiple-cathode vacuum arc plasma source was coupled to a 50 cm diameter beam extractor (multiple aperture, accel-decel configuration) operated at a net extraction voltage of up to 50 kV. The metal ion species chosen were Ni and Ta. The mean ion charge state for Ni and Ta vacuum arc plasmas is 1.8 and 2.9, respectively, and so the mean ion energies were up to about 90 and 145 keV, respectively. The ion source was operated in a repetitively pulsed mode with pulse length 250 μs and repetition rate several pulses per second. The extracted beam had a gaussian profile with FWHM about 35 cm, giving a nominal beam area of about 1,000 cm 2 . The current of Ni or Ta metal ions in the beam was up to several amperes. The targets for the ion implantation were a number of 24-inch long, highly polished Cu rails from an electromagnetic rail gun. The rails were located about 80 cm away from the ion source extractor grids, and were moved across a diameter of the vessel in such a way as to maximize the uniformity of the implant along the rail. The saturation retained dose for Ta was limited to about 4 x 10 16 cm -2 because of the rather severe sputtering, in accordance with the theoretical expectations for these implantation conditions. Here they describe the ion source, the implantation procedure, and the kinds of implants that can be produced in this way

  17. Modification of medical metals by ion implantation of copper

    Science.gov (United States)

    Wan, Y. Z.; Xiong, G. Y.; Liang, H.; Raman, S.; He, F.; Huang, Y.

    2007-10-01

    The effect of copper ion implantation on the antibacterial activity, wear performance and corrosion resistance of medical metals including 317 L of stainless steels, pure titanium, and Ti-Al-Nb alloy was studied in this work. The specimens were implanted with copper ions using a MEVVA source ion implanter with ion doses ranging from 0.5 × 10 17 to 4 × 10 17 ions/cm 2 at an energy of 80 keV. The antibacterial effect, wear rate, and inflexion potential were measured as a function of ion dose. The results obtained indicate that copper ion implantation improves the antibacterial effect and wear behaviour for all the three medical materials studied. However, corrosion resistance decreases after ion implantation of copper. Experimental results indicate that the antibacterial property and corrosion resistance should be balanced for medical titanium materials. The marked deteriorated corrosion resistance of 317 L suggests that copper implantation may not be an effective method of improving its antibacterial activity.

  18. Method for removing metal ions from solution with titanate sorbents

    Science.gov (United States)

    Lundquist, Susan H.; White, Lloyd R.

    1999-01-01

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

  19. Ion spectra of the metal vapor vacuum arc ion source with compound and alloy cathodes

    Science.gov (United States)

    Sasaki, Jun; Brown, Ian G.

    1990-01-01

    In metal vapor vacuum arc (MEVVA) ion sources, vacuum arc plasma with cathodes of single, pure elements has been utilized for the production of metal ions. In this study, we have investigated the charge state distributions of ions produced in vacuum arc plasmas in a MEVVA ion source for the case when the cathode is an alloy or a compound material. The ion charge state spectra were analyzed by means of a time-of-flight apparatus. We have compared the ion spectra for a cathode of an alloy or a compound material with its constituent elements: TiC/TiN/TiO2/Ti/C, SiC/Si/C, WC/W/C U/UN/(UN-ZrC)/Zr/C, and brass/Zn/Cu. We find that the MEVVA produces ions of all constituent elements in the compound and the alloy cathodes. The charge state distribution of each element differs, however, from the charge state distribution obtained in the vacuum arc with a cathode made of the pure, single constituent element. Fractional values of the total ion numbers of each constituent element in the extracted beam depart from the stoichiometry of the elements in the cathode material. In an operation with a TiC cathode, we irradiated a 304 stainless-steel plate with the extracted beam. Results from glow-discharge spectroscopy (GDS) of the surface show that both titanium and carbon are implanted in the substrate after the irradiation.

  20. Metal ion levels and lymphocyte counts

    DEFF Research Database (Denmark)

    Penny, Jeannette Ø; Varmarken, Jens-Erik; Ovesen, Ole

    2013-01-01

    . RESULTS: The T-lymphocyte counts for both implant types declined over the 2-year period. This decline was statistically significant for CD3(+)CD8(+) in the THA group, with a regression coefficient of -0.04 × 10(9)cells/year (95% CI: -0.08 to -0.01). Regression analysis indicated a depressive effect...... of cobalt ions in particular on T-cells with 2-year whole-blood cobalt regression coefficients for CD3+ of -0.10 (95% CI: -0.16 to -0.04) × 10(9) cells/parts per billion (ppb), for CD3+CD4+ of -0.06 (-0.09 to -0.03) × 10(9) cells/ppb, and for CD3(+)CD8(+) of -0.02 (-0.03 to -0.00) × 10(9) cells...

  1. Thin film separators with ion transport properties for energy applications

    Science.gov (United States)

    Li, Zhongyuan

    2017-09-01

    Recent years, along with the increasing need of energy, energy storage also becomes a challenging problem which we need to deal with. The batterieshave a good developing prospect among energy storage system in storing energy such as wind, solar and geothermal energy. One hurdle between the lab-scale experiment and industry-scale application of the advanced batteries is the urgent need for limiting charging capacity degradation and improving cycling stability, known as the shuttle effect in lithium-sulfur batteries or electroosmotic drag coefficient in fuel-cell batteries. The microporous separator between the cathode and anode could be molecular engineered to possessesion selective permeation properties, which can greatly improves the energy efficiency and extends application range of the battery. The present review offers the fundamental fabrication methods of separator film with different material. The review also contains the chemical or physical structure of different materials which are used in making separator film. A table offers the reader a summary of properties such as ionic conductivity, ionic exchange capacity and current density etc.

  2. Comparison of metal ion concentrations and implant survival after total hip arthroplasty with metal-on-metal versus metal-on-polyethylene articulations

    OpenAIRE

    Dahlstrand, Henrik; Stark, André; Wick, Marius C; Anissian, Lucas; Hailer, Nils P; Weiss, Rüdiger J

    2017-01-01

    Background and purpose Large metal-on-metal (MoM) articulations are associated with metal wear and corrosion, leading to increased metal ion concentrations and unacceptable revision rates. There are few comparative studies of 28-mm MoM articulations with conventional metal-on-polyethylene (MoP) couplings. We present a long-term follow-up of a randomized controlled trial comparing MoM versus MoP 28-mm articulations, focused on metal ions and implant survival. Patients and methods 85 patients w...

  3. Interaction of Metal Ions with Biomolecular Ligands: How Accurate Are Calculated Free Energies Associated with Metal Ion Complexation?

    Czech Academy of Sciences Publication Activity Database

    Gutten, Ondrej; Beššeová, Ivana; Rulíšek, Lubomír

    2011-01-01

    Roč. 115, č. 41 (2011), s. 11394-11402 ISSN 1089-5639 R&D Projects: GA MŠk LC512 Institutional research plan: CEZ:AV0Z40550506 Keywords : metal-ion selectivity * theoretical calculations * stability constants Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.946, year: 2011

  4. Kinetic study of heavy metal ions removal by ion exchange in batch conical air spouted bed

    Directory of Open Access Journals (Sweden)

    T.M. Zewail

    2015-03-01

    Full Text Available Spouted bed contactor is a hybrid of fixed and fluidized bed contactors, which retains the advantages of each with good hydrodynamic conditions. The aim of the present study is to investigate the performance of a batch conical air spouted vessel for heavy metal removal by strong cation exchange resins (AMBERJET 1200 Na. The effect of various parameters such as type of heavy metal ions (Ni+2 and Pb+2, contact time, superficial air velocity and initial heavy metal ion concentration on % heavy metal ion removal has been investigated. It has been found that under optimum conditions 98% and 99% removal of Ni+2 and Pb+2 were achieved respectively. Several kinetic models were used to test the experimental data and to examine the controlling mechanism of the sorption process. The present results of Ni+2 and Pb+2 well fit pseudo second order kinetic model with a high correlation coefficient. Both film diffusion and intra-particle diffusion contribute to the ion exchange process. The present study revealed that spouted bed vessel may provide an effective alternative for conducting ion exchange reactions.

  5. Ion conducting polymers and polymer blends for alkali metal ion batteries

    Science.gov (United States)

    DeSimone, Joseph M.; Pandya, Ashish; Wong, Dominica; Vitale, Alessandra

    2017-08-29

    Electrolyte compositions for batteries such as lithium ion and lithium air batteries are described. In some embodiments the compositions are liquid compositions comprising (a) a homogeneous solvent system, said solvent system comprising a perfluropolyether (PFPE) and polyethylene oxide (PEO); and (b) an alkali metal salt dissolved in said solvent system. In other embodiments the compositions are solid electrolyte compositions comprising: (a) a solid polymer, said polymer comprising a crosslinked product of a crosslinkable perfluropolyether (PFPE) and a crosslinkable polyethylene oxide (PEO); and (b) an alkali metal ion salt dissolved in said polymer. Batteries containing such compositions as electrolytes are also described.

  6. In vitro cytotoxicity of metallic ions released from dental alloys.

    Science.gov (United States)

    Milheiro, Ana; Nozaki, Kosuke; Kleverlaan, Cornelis J; Muris, Joris; Miura, Hiroyuki; Feilzer, Albert J

    2016-05-01

    The cytotoxicity of a dental alloy depends on, but is not limited to, the extent of its corrosion behavior. Individual ions may have effects on cell viability that are different from metals interacting within the alloy structure. We aimed to investigate the cytotoxicity of individual metal ions in concentrations similar to those reported to be released from Pd-based dental alloys on mouse fibroblast cells. Metal salts were used to prepare seven solutions (concentration range 100 ppm-1 ppb) of the transition metals, such as Ni(II), Pd(II), Cu(II), and Ag(I), and the metals, such as Ga(III), In(III), and Sn(II). Cytotoxicity on mouse fibroblasts L929 was evaluated using the MTT assay. Ni, Cu, and Ag are cytotoxic at 10 ppm, Pd and Ga at 100 ppm. Sn and In were not able to induce cytotoxicity at the tested concentrations. Transition metals were able to induce cytotoxic effects in concentrations similar to those reported to be released from Pd-based dental alloys. Ni, Cu, and Ag were the most cytotoxic followed by Pd and Ga; Sn and In were not cytotoxic. Cytotoxic reactions might be considered in the etiopathogenesis of clinically observed local adverse reactions.

  7. Adsorptive Removal of Metal Ions from Water using Functionalized Biomaterials.

    Science.gov (United States)

    Deshpande, Kanchanmala

    2017-01-01

    Synthesis and modification of cost-effective sorbents for removing heavy metals from water resources is an area of significance. It had been reported that materials with biological origins, such as agricultural and animal waste, are excellent alternatives to conventional adsorbents due to their higher affinity, capacity and selectivity towards metal ions. These properties of biomaterials help to reduce or detoxify metal ions concentration in contaminated water to acceptable regulatory standards. Synthesis of novel, efficient, cost effective, eco-friendly biomaterials for heavy metal adsorption from water is still an area of challenge. In this comprehensive review, acompilation of patents as well as published articles is carried out to outline the properties of different biomaterials based on their precursors along withdetailed description of biomaterial morphology and various surface modification approaches. A detailed study of the performance of adsorbents and the role of physical and chemical modification in terms of enhancing their potential for metal adsorption from water is compiled here. The factors affecting adsorption behavior i.e., capacity and affinity of e biomaterials is also compiled. This paper presents a concise review of reported studies on the synthesis and modification of biomaterials, their use for heavy metal removal from waters and future prospects of this technology. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

  8. High Resolution Separations and Improved Ion Production and Transmission in Metabolomics

    Energy Technology Data Exchange (ETDEWEB)

    Metz, Thomas O.; Page, Jason S.; Baker, Erin Shammel; Tang, Keqi; Ding, Jie; Shen, Yufeng; Smith, Richard D.

    2008-03-31

    The goal of metabolomics experiments is the detection and quantitation of as many sample components as reasonably possible in order to identify “features” that can be used to characterize the samples under study. When utilizing electrospray ionization to produce ions for analysis by mass spectrometry (MS), it is imperative that metabolome sample constituents be efficiently separated prior to ion production, in order to minimize the phenomenon of ionization suppression. Similarly, optimization of the MS inlet can lead to increased measurement sensitivity. This review will focus on the role of high resolution liquid chromatography (LC) separations in conjunction with improved ion production and transmission for LC-MS-based metabolomics.

  9. Liquid metal alloy ion sources—An alternative for focussed ion beam technology

    International Nuclear Information System (INIS)

    Bischoff, Lothar; Mazarov, Paul; Bruchhaus, Lars; Gierak, Jacques

    2016-01-01

    Today, Focused Ion Beam (FIB) processing is nearly exclusively based on gallium Liquid Metal Ion Sources (LMIS). But, many applications in the μm- or nm range could benefit from ion species other than gallium: local ion implantation, ion beam mixing, ion beam synthesis, or Focused Ion Beam Lithography (IBL). Therefore, Liquid Metal Alloy Ion Sources (LMAIS) represent a promising alternative to expand the remarkable application fields for FIB. Especially, the IBL process shows potential advantages over, e.g., electron beam or other lithography techniques: direct, resistless, and three-dimensional patterning, enabling a simultaneous in-situ process control by cross-sectioning and inspection. Taking additionally into account that the used ion species influences significantly the physical and chemical nature of the resulting nanostructures—in particular, the electrical, optical, magnetic, and mechanic properties leading to a large potential application area which can be tuned by choosing a well suited LMAIS. Nearly half of the elements of the periodic table are recently available in the FIB technology as a result of continuous research in this area during the last forty years. Key features of a LMAIS are long life-time, high brightness, and stable ion current. Recent developments could make these sources feasible for nano patterning issues as an alternative technology more in research than in industry. The authors will review existing LMAIS, LMIS other than Ga, and binary and ternary alloys. These physical properties as well as the fabrication technology and prospective domains for modern FIB applications will similarly be reviewed. Other emerging ion sources will be also presented and their performances discussed.

  10. Effect of Oxide Nanoparticles on Thermal and Mechanical Properties of Electrospun Separators for Lithium-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Marco Zaccaria

    2012-01-01

    Full Text Available This study reports the fabrication and characterization of poly(ethylene oxide (PEO and poly(vinylidenefluoride-co-chlorotrifluoroethylene (PVDF-CTFE nanofibrous separators for lithium-ion batteries loaded with different amounts of fumed-silica and tin oxide nanoparticles. Membrane morphological characterization (SEM, TEM showed the presence of good-quality nanofibres containing nanoparticles. Thermal degradation and membrane mechanical properties were also investigated, and a remarkable effect of nanoparticle addition on membrane mechanical properties was found. In particular, PEO membranes were strengthened by the addition of metal oxide, whereas PVDF-CTFE membranes acquired ductility.

  11. Ion beam mixing isotopic metal bilayers

    Energy Technology Data Exchange (ETDEWEB)

    Fell, C.J. [Newcastle Univ., NSW (Australia). Dept. of Physics; Kenny, M.J. [CSIRO, Lindfield, NSW (Australia). Div. of Applied Physics

    1993-12-31

    In order to obtain an insight into the mechanisms of ion-solid interactions, bilayer targets can be prepared from two different isotopes. A mixing study SIMS is to be carried out using specially grown monocrystalline bilayers of {sup 58}Ni / {sup 60}Ni. An important aspect of the work is the preparation of high quality single-crystal thin films. The Ni layers will be grown on the (110) surface of pure Ni and verified for crystallinity using Reflection High-Energy Electron Diffraction and Rutherford Backscattering channelling analysis. The Pd bilayers will be grown on a Pd (100) surface. RHEED will be used to confirm the two-dimensional crystallinity of the surface before and after deposition of each layer, and channelling used to confirm bulk film crystallinity. Single crystal substrates are currently being prepared. Analysis of the Ni (110) surface using RHEED at 9 kV shows a streak spacing which corresponds to a lattice spacing of 2.47 {+-} 0.09 Angstroms. 9 refs., 1 fig.

  12. Mesotubular-Structured Hybrid Membrane Nanocontainer for Periodical Monitoring, Separation, and Recovery of Cobalt Ions from Water.

    Science.gov (United States)

    El-Safty, Sherif A; Sakai, Masaru; Selim, Mahmoud M; Alhamid, Abdulaziz A

    2015-09-01

    Exposure to toxins can cause deleterious effects even at very low concentrations. We have developed an optical sensor, filter, and extractor (i.e., containerlike) in a nanoscale membrane (NSM) for the ultratrace sensing, separation, and recovery of Co(2+) ions from water. The design of the NSM is successfully controlled by dense decoration of a hydrophobic oil-hydrophilic receptor onto mesoscale tubular-structured silica nanochannels made of a hybrid anodic alumina membrane. The particular structure of the nanocontainer is ideal to control the multiple functions of the membrane, such as the optical detection/recognition, rejection/permeation, and recovery of Co(2+) species in a single step. A typical sensor, filter, and extractor assessment experiment was performed by using a benchtop contact time technique and a flow-through cell detector to allow for precise control of the optical detection and exclusive rejection of target ions and the permeation of nontarget metal ions in water. This nanocontainer membrane has great potential to meet the increasing needs of purification and separation of Co(2+) ions. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. [Applications of metal ions and their complexes in medicine I].

    Science.gov (United States)

    Nagy, László; Csintalan, Gabriella; Kálmán, Eszter; Sipos, Pál; Szvetnik, Attila

    2003-01-01

    The "inorganic medical chemistry" is a rapidly developing field with enormous potential for applications, which offers new possibilities to the pharmaceutical industry. For example, the titanocene dichloride is already in clinical use, and antimetastatic activity of a range of Ru(III) complexes is also well established. There are ways to minimize the toxicity of Gd(III) complexes and therefore they can be safely injected as MRI contrast agents. The so called "ligand design" allows paramagnetic ions to be targeted to specific organs. Such designed ligands also enable the targeting of radiodiagnostic (99mTc) and radiotherapeutic (186Re) isotopes. There is a significant progress in understanding the coordination chemistry and biochemistry of metal ion(s) containing complexes such as Au antiarthritic and Bi antiulcer drugs. Further, currently developing areas include Mn (SOD mimics), V (insulin mimics), Ru (NO scavengers), Ln-based photosensitizers, metal-targeted organic agents and the Fe overload. The expanding knowledge of the role of metals in biochemistry is expected to provide scope for the design of new drugs in many other areas too, for example neuropharmaceutical and antiaffective agents. Progress in coordination chemistry is strongly dependent on understanding not only the thermodynamics of reactions, but also the kinetics of metal complexes under biologically relevant conditions.

  14. Rate-dependent performance of ion chambers for particle-ID at the GSI fragment separator

    Energy Technology Data Exchange (ETDEWEB)

    Hucka, Jan-Paul; Allred, Timothy; Enders, Joachim [Institut fuer Kernphysik, TU Darmstadt (Germany); Gernhaeuser, Roman; Maurus, Steffen [Physik Department, TU Muenchen (Germany); Nociforo, Chiara; Pietri, Stephane; Prochazka, Andrej [GSI Helmholtzzentrum fuer Schwerionenforschung (Germany)

    2015-07-01

    At the GSI Fragment Separator (FRS), multi-sampling ion chambers (MUSIC) employing a Frisch grid are used for charge identification of secondary ion beams. At the FAIR Super-FRS, higher rates are expected, and an event-by-event determination of the charge of secondary ions will be needed at rates of several 100000 events per second. The comparison of results from test measurements for the MUSIC performance with that of a recently constructed tilted-electrode gas ion chamber (TEGIC), which was designed similar to the one discussed, is presented.

  15. Ionic-Liquid-Based Acidic Aqueous Biphasic Systems for Simultaneous Leaching and Extraction of Metallic Ions.

    Science.gov (United States)

    Gras, Matthieu; Papaiconomou, Nicolas; Schaeffer, Nicolas; Chainet, Eric; Tedjar, Farouk; Coutinho, Joao A P; Billard, Isabelle

    2018-02-05

    The first instance of an acidic aqueous biphasic system (AcABS) based on tributyltetradecyl phosphonium chloride ([P 44414 ][Cl]) and an acid is here reported. This AcABS exhibits pronounced thermomorphic behavior and is shown to be applicable to the extraction of metal ions from concentrated acidic solutions. Metal ions such as cobalt(II), iron(III), platinum(IV) and nickel(II) are found to partition preferentially to one of the phases of the acidic aqueous biphasic system and it is here shown that it successfully allows the difficult separation of Co II from Ni II , here studied at 24 and 50 °C. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Polymer filtration systems for dilute metal ion recovery

    Energy Technology Data Exchange (ETDEWEB)

    Smith, B.F.; Robison, T.W.; Jarvinen, G.D.

    1998-12-01

    Scientists at Los Alamos National Laboratory have developed a metal recovery system that meets the global treatment demands for all kinds of industrial and metal-processing streams. The Polymer Filtration (PF) System--a process that is easily operated and robust--offers metal-finishing businesses a convenient and inexpensive way to recover and recycle metal ions in-house, thus reducing materials costs, waste removal costs, and industrial liability. As a valuable economic and environmental asset, the PF System has been named a winner of a 1995 R and D 100 Award. These awards are presented annually by R and D Magazine to the one hundred most significant technical innovations of the year. The PF System is based on the use of water-soluble metal-binding polymers and on advanced ultrafiltration membranes. Customers for this technology will receive new soluble polymers, especially formulated for their waste stream, and the complete PF processing unit: a reaction reservoir, pumps, plumbing, controls, and the advanced ultrafiltration membranes, all in a skid mounted frame. Metal-bearing waste water is treated in the reaction reservoir, where the polymer binds with the metal ions under balanced acid/base conditions. The reservoir fluid is then pumped through the ultrafiltration system--a cartridge packed with ultrafiltration membranes shaped in hollow fibers. As the fluid travels inside the fiber, water and other small molecules--simple salts such as calcium and sodium, for example--pass through the porous membrane walls of the fibers and are discharged through the outlet as permeate. The polymer-bound metal, which is too large to pass through the pores, is both purified and concentrated inside the hollow fibers and is returned to the fluid reservoir for further waste water treatment.

  17. Electron emission during multicharged ion-metal surface interactions

    International Nuclear Information System (INIS)

    Zeijlmans van Emmichoven, P.A.; Havener, C.C.; Hughes, I.G.; Overbury, S.H.; Robinson, M.T.; Zehner, D.M.; Meyer, F.W.

    1992-01-01

    The electron emission during multicharged ion-metal surface interactions will be discussed. The interactions lead to the emission of a significant number of electrons. Most of these electrons have energies below 30 eV. For incident ions with innershell vacancies the emission of Auger electrons that fill these vacancies has been found to occur mainly below the surface. We will present recently measured electron energy distributions which will be used to discuss the mechanisms that lead to the emission of Auger and of low-energy electrons

  18. Wear properties of metal ion implanted 4140 steel

    International Nuclear Information System (INIS)

    Evans, P.J.; Paoloni, F.J.

    1994-01-01

    AISI type 4140 (high tensile) steel has been implanted with tungsten and titanium using a metal vapour vacuum arc ion source. Doses in the range (1-5)x10 16 ionscm -2 were implanted to a depth of approximately 30nm. The relative wear resistance between non-implanted and implanted specimens has been estimated using pin-on-disc and abrasive wear tests. Implantation of titanium decreased the area of wear tracks by a factor of 5 over unimplanted steel. In some cases the steel was also hardened by a liquid carburization treatment before implantation. Abrasion tests revealed a further improvement in wear resistance on this material following ion irradiation. ((orig.))

  19. Hydrometallurgical recovery of metal values from sulfuric acid leaching liquor of spent lithium-ion batteries

    International Nuclear Information System (INIS)

    Chen, Xiangping; Chen, Yongbin; Zhou, Tao; Liu, Depei; Hu, Hang; Fan, Shaoyun

    2015-01-01

    Highlights: • Selective precipitation and solvent extraction were adopted. • Nickel, cobalt and lithium were selectively precipitated. • Co-D2EHPA was employed as high-efficiency extraction reagent for manganese. • High recovery percentages could be achieved for all metal values. - Abstract: Environmentally hazardous substances contained in spent Li-ion batteries, such as heavy metals and nocuous organics, will pose a threat to the environment and human health. On the other hand, the sustainable recycling of spent lithium-ion batteries may bring about environmental and economic benefits. In this study, a hydrometallurgical process was adopted for the comprehensive recovery of nickel, manganese, cobalt and lithium from sulfuric acid leaching liquor from waste cathode materials of spent lithium-ion batteries. First, nickel ions were selectively precipitated and recovered using dimethylglyoxime reagent. Recycled dimethylglyoxime could be re-used as precipitant for nickel and revealed similar precipitation performance compared with fresh dimethylglyoxime. Then the separation of manganese and cobalt was conducted by solvent extraction method using cobalt loaded D2EHPA. And McCabe–Thiele isotherm was employed for the prediction of the degree of separation and the number of extraction stages needed at specific experimental conditions. Finally, cobalt and lithium were sequentially precipitated and recovered as CoC 2 O 4 ⋅2H 2 O and Li 2 CO 3 using ammonium oxalate solution and saturated sodium carbonate solution, respectively. Recovery efficiencies could be attained as follows: 98.7% for Ni; 97.1% for Mn, 98.2% for Co and 81.0% for Li under optimized experimental conditions. This hydrometallurgical process may promise a candidate for the effective separation and recovery of metal values from the sulfuric acid leaching liquor

  20. Hydrometallurgical recovery of metal values from sulfuric acid leaching liquor of spent lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xiangping; Chen, Yongbin; Zhou, Tao, E-mail: zhoutao@csu.edu.cn; Liu, Depei; Hu, Hang; Fan, Shaoyun

    2015-04-15

    Highlights: • Selective precipitation and solvent extraction were adopted. • Nickel, cobalt and lithium were selectively precipitated. • Co-D2EHPA was employed as high-efficiency extraction reagent for manganese. • High recovery percentages could be achieved for all metal values. - Abstract: Environmentally hazardous substances contained in spent Li-ion batteries, such as heavy metals and nocuous organics, will pose a threat to the environment and human health. On the other hand, the sustainable recycling of spent lithium-ion batteries may bring about environmental and economic benefits. In this study, a hydrometallurgical process was adopted for the comprehensive recovery of nickel, manganese, cobalt and lithium from sulfuric acid leaching liquor from waste cathode materials of spent lithium-ion batteries. First, nickel ions were selectively precipitated and recovered using dimethylglyoxime reagent. Recycled dimethylglyoxime could be re-used as precipitant for nickel and revealed similar precipitation performance compared with fresh dimethylglyoxime. Then the separation of manganese and cobalt was conducted by solvent extraction method using cobalt loaded D2EHPA. And McCabe–Thiele isotherm was employed for the prediction of the degree of separation and the number of extraction stages needed at specific experimental conditions. Finally, cobalt and lithium were sequentially precipitated and recovered as CoC{sub 2}O{sub 4}⋅2H{sub 2}O and Li{sub 2}CO{sub 3} using ammonium oxalate solution and saturated sodium carbonate solution, respectively. Recovery efficiencies could be attained as follows: 98.7% for Ni; 97.1% for Mn, 98.2% for Co and 81.0% for Li under optimized experimental conditions. This hydrometallurgical process may promise a candidate for the effective separation and recovery of metal values from the sulfuric acid leaching liquor.

  1. Ion exchange of some transition metal cations on hydrated titanium dioxide in aqueous ammonia solutions

    International Nuclear Information System (INIS)

    Bilewicz, A.; Narbutt, J.; Dybczynski, R.

    1992-01-01

    The adsorption of transition metal cations on hydrated titanium dioxide in complexing ammonia and amine solutions has been studied as a function of ammonia (amine) concentration. The relationships between the distribution coefficients and ammonia concentration as well as the effects of various amines on sorption of transition metals indicate that a coordinate bond is formed between the metal ions and the hydroxy groups of the sorbent. The distribution coefficients of silver(I) and cobalt(II), which form strong ammonia complexes in aqueous solutions, decrease with increasing concentration of ammonia already at concentrations exceeding 10 -3 *mol*dm -3 . Cations of zinc, manganese and mercury which form much weaker ammonia complexes do not exhibit any effect of ammonia concentration in the whole range investigated. In the case of sorption of macroamounts of ammonia or amine complexes of silver, the molecular sieve effect plays an important role. The differences in the affinity of hydrated titanium dioxide for ammonia solvates of various transition metal ions can serve as a tool for effective separation of these ions in ammonia solutions. (author) 10 refs.; 4 figs.; 1 tab

  2. Development of carbon and metallic nano particle composite materials for the determination of uranium and other heavy metal ions

    International Nuclear Information System (INIS)

    Sahoo, S.; Dey, M.K.; Satpati, A.K.; Reddy, A.V.R.

    2014-01-01

    Carbon and metallic nano particle based composite materials were developed and characterised for the determination of heavy metal ions and uranium in trace concentration levels. Composite material were electrodeposited on the substrate electrode and applied for the electrochemical determination of metal ions. Electrodeposition parameters to synthesise the composite material and the analytical parameters for determination were optimised. (author)

  3. Unique battery with an active membrane separator having uniform physico-chemically functionalized ion channels and a method making the same

    Science.gov (United States)

    Gerald, II, Rex E.; Ruscic, Katarina J [Chicago, IL; Sears, Devin N [Spruce Grove, CA; Smith, Luis J [Natick, MA; Klingler, Robert J [Glenview, IL; Rathke, Jerome W [Homer Glen, IL

    2012-02-21

    The invention relates to a unique battery having an active, porous membrane and method of making the same. More specifically the invention relates to a sealed battery system having a porous, metal oxide membrane with uniform, physicochemically functionalized ion channels capable of adjustable ionic interaction. The physicochemically-active porous membrane 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. 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.

  4. Metal ion toxins and brain aquaporin-4 expression: an overview

    Directory of Open Access Journals (Sweden)

    Adriana eXimenes-Da-Silva

    2016-06-01

    Full Text Available Metal ions such as iron, zinc, and manganese are essential to metabolic functions, protein synthesis, neurotransmission, and antioxidant neuroprotective mechanisms. Conversely, non-essential metals such as mercury and lead are sources of human intoxication due to occupational activities or environmental contamination. Essential or non-essential metal accumulation in the central nervous system (CNS results in changes in blood-brain barrier (BBB permeability, as well as triggering microglia activation and astrocyte reactivity and changing water transport through the cells, which could result in brain swelling. Aquaporin-4 is the main water channel in the CNS, is expressed in astrocyte foot processes in brain capillaries and along the circumventricular epithelium in the ventricles, and has important physiological functions in maintaining brain osmotic homeostasis and supporting brain excitability through regulation of the extracellular space. Some evidence has pointed to a role of AQP4 during metal intoxication in the brain, where it may act in a dual form as a neuroprotector or a mediator of the development of oxidative stress in neurons and astrocytes, resulting in brain swelling and neuronal damage. This mini-review presents the way some metal ions affect changes in AQP4 expression in the CNS and discuss the ways in which water transport in brain cells can be involved in brain damage.

  5. The Corrosion Protection of Metals by Ion Vapor Deposited Aluminum

    Science.gov (United States)

    Danford, M. D.

    1993-01-01

    A study of the corrosion protection of substrate metals by ion vapor deposited aluminum (IVD Al) coats has been carried out. Corrosion protection by both anodized and unanodized IVD Al coats has been investigated. Base metals included in the study were 2219-T87 Al, 7075-T6 Al, Titanium-6 Al-4 Vanadium (Ti-6Al-4V), 4130 steel, D6AC steel, and 4340 steel. Results reveal that the anodized IVD Al coats provide excellent corrosion protection, but good protection is also achieved by IVD Al coats that have not been anodized.

  6. Selective extraction of metal ions with polymeric extractants by ion exchange/redox

    Science.gov (United States)

    Alexandratos, Spiro D.

    1987-01-01

    The specification discloses a method for the extraction of metal ions having a reduction potential of above about +0.3 from an aqueous solution. The method includes contacting the aqueous solution with a polymeric extractant having primary phosphinic acid groups, secondary phosphine oxide groups, or both phosphinic acid and phosphine oxide groups.

  7. Kinetic modeling of metal ion transport for desorption of Pb(II) ion ...

    African Journals Online (AJOL)

    The kinetics of desorption of lead (II) ion from metal loaded adsorbent of mercaptoacetic acid modified and unmodified oil palm (Elaeis guineensis) fruit fiber was studied using different solutions, at different contact times. At the end of 25 minutes, 79.19%, 75.99%, 57.14%, 50.56% and 32.72% of Pb2+ were desorbed using ...

  8. Sources and speciation of heavy metals in municipal solid waste (MSW) and its effect on the separation technique

    Energy Technology Data Exchange (ETDEWEB)

    Biollaz, S.; Ludwig, Ch.; Stucki, S. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    A literature search was carried out to determine sources and speciation of heavy metals in MSW. A combination of thermal and mechanical separation techniques is necessary to achieve the required high degrees of metal separation. Metallic goods should be separated mechanically, chemically bound heavy metals by a thermal process. (author) 1 fig., 1 tab., 6 refs.

  9. Separation of rare-earth (RE) ions by flotation with the aid of citric acid and hexadecylamine

    International Nuclear Information System (INIS)

    Skrylev, L.D.; Sazonova, V.F.; Pavlenko, S.N.; Karpenko, L.I.

    1989-01-01

    The aim of the present work was to develop further the flotation method for separating RE ions, namely, to examine the possibility of separating Re ions by converting them into citrate complexes and subsequently binding them with the aid of hexadecylamine in difficultly soluble and easily floatable compounds, sublates. Thus, these investigations showed that it is possible in principle to separate RE ions by conversion into citrate complexes followed by flotation separation of the latter from solutions with the aid of hexadecylamine

  10. Multiply charged metal ions in high current pulsed vacuum arcs

    Science.gov (United States)

    Yushkov, G. Yu.; Nikolaev, A. G.; Frolova, V. P.; Oks, E. M.; Rousskikh, A. G.; Zhigalin, A. S.

    2017-12-01

    We show that vacuum arc plasma discharges with a current of several kiloamperes and duration of a few microseconds can generate multiply charged metal ions with charge states greater than 10+. The physical mechanism behind this is discussed, suggesting an optimum arc current for higher charge states depending on the pulse duration and cathode material. Measurements of ion mass-to-charge ratio and images taken with nanosecond resolution suggest that, higher charge state ions are produced at characteristic distances of ˜10 mm from the cathode as the arc current peaks, and the process responsible for their generation is additional ionization as the discharge is pinched by its self-magnetic field. The maximum and mean ion charge states reveal a considerable increase for the all cathode materials studied: magnesium, aluminum, zirconium, tin, tantalum, gold, lead, and bismuth. For bismuth ions, the maximum charge state reaches a record-breaking value of 17+ and the mean of the charge state distribution is 12.6+. The results obtained are of interest for vacuum arc discharge physics and for ion beam technologies.

  11. Adsorption of heavy metal ions by activated charcoal

    International Nuclear Information System (INIS)

    Fujikawa, Mitsuo

    1978-01-01

    The adsorption effect was measured for several kinds of heavy metal ions, Pb 2+ , Cd 2+ , Cu 2+ and Zn 2+ by passing them through activated charcoal beds and changing the pH values of solutions. The test procedure is to keep the pH value of solution more than 10 at first, filter heavy metal hydroxide deposit, measure the remaining ion concentration in filtrate, and also test the influence of the addition of alkali to each kind of ions. The individual test procedure for each kind of ions is explained. As for the Cd ions, after the detailed experimental procedure is explained, the adsorption characteristic line is shown as the relation between the adsorption quantity and the equilibrium concentration of Cd 2+ . The similar test procedure and the adsorption characteristic lines are shown and evaluated about Pb 2+ , Cu 2+ and Zn 2+ . These lines are all linear, but have different adsorption quantity and inclination in relation to heavy metal ion concentration. Concerning the influence of pH to adsorption, the characteristics of pH increase are presented, when alkali is added by various quantities to Zn 2+ , Cu 2+ , Pb 2+ and Cd 2+ . The pH of Pb 2+ increased to about 10 by adding 0.4 cc alkali and saturates, but the pH of the other ions did not saturate by adding less than 1.5 cc alkali. When the water containing heavy metals are treated, Cd 2+ , Pb 2+ , Cu 2+ and Zn 2+ are removed almost satisfactorily by passing them through active charcoal filters and keeping pH at 10. The experimental concentrations are 0.05 ppm at pH 10 in Cd, 0.86 ppm at 10.3 in Pb, 0 ppm at pH 9.6 in Cu, 0.06 ppm at pH 8.8 and 12.4 ppm at pH 9.8 in Zn. (Nakai, Y.)

  12. Lithium metal doped electrodes for lithium-ion rechargeable chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Gao; Battaglia, Vince; Wang, Lei

    2016-09-13

    An embodiment of the invention combines the superior performance of a polyvinylidene difluoride (PVDF) or polyethyleneoxide (POE) binder, the strong binding force of a styrene-butadiene (SBR) binder, and a source of lithium ions in the form of solid lithium metal powder (SLMP) to form an electrode system that has improved performance as compared to PVDF/SBR binder based electrodes. This invention will provide a new way to achieve improved results at a much reduced cost.

  13. Gas porosity in metals and alloys irradiated by helium ions

    International Nuclear Information System (INIS)

    Kalin, B.A.; Korshunov, S.N.; Chernov, I.I.

    1987-01-01

    Experimental studies of the development of gas porosity in metals and alloys during irradiation with helium ions up to high doses and during post-irradiation annealings, are reviewed. The main theoretical problems of the mechanisms of bubble formation and growth, the regularities and peculiarities of bubble development in a thin near-the surface layer during the introduction of helium with the energy of tens of kiloelectron volt, are considered

  14. Towards the role of metal ions in the structural variability of proteins: CdII speciation of a metal ion binding loop motif

    DEFF Research Database (Denmark)

    Jancsó, Attila; Szunyogh, Dániel; Gyurcsik, Béla

    2011-01-01

    A de novo designed dodecapeptide (HS), inspired by the metal binding loops of metal-responsive transcriptional activators, was synthesized. The aim was to create a model system for structurally promiscuous and intrinsically unstructured proteins, and explore the effect of metal ions on their stru...... the peptide is exchanging between a number of structures also in its metal ion bound state(s), as indicated by NMR and PAC data. © 2011 The Royal Society of Chemistry....

  15. In situ NMR measurement of macromolecule-bound metal ion concentrations.

    Science.gov (United States)

    Kozlyuk, Natalia; Sengupta, Suvrajit; Lupták, Andrej; Martin, Rachel W

    2016-04-01

    Many nucleic acids and proteins require divalent metal ions such as Mg(2+) and Ca(2+) for folding and function. The lipophilic alignment media frequently used as membrane mimetics also bind these divalent metals. Here we demonstrate the use of (31)P NMR spectrum of a metal ion chelator (deoxycytidine diphosphate) to measure the bound [Mg(2+)] and [Ca(2+)] in situ for several biological model systems at relatively high divalent ion concentrations (1-10 mM). This method represents a general approach to measuring divalent metal ion binding in NMR samples where the amount and type of metal ion added to the system is known.

  16. Separation of matrix alloy and reinforcement from aluminum metal ...

    Indian Academy of Sciences (India)

    TECS

    . The application of metal matrix composites (MMCs) in many engineering components has increased over the last few years, particularly in the automobile industry as drive shafts, engine and brake components (Chawla and Chawla. 2006).

  17. Spectrophotometric determination of some metal ions using hydrazones

    International Nuclear Information System (INIS)

    Mohammed, M. S.

    2000-05-01

    In this research many starting materials were prepared, like methyl salicylate and salicylic acid hydrazide from which different derivatives of hydrazones were synthesized by coupling with carbonyl compounds like benzil monoxime and benzil mono hydrazone which are prepared and others like salicylaldehyde and benzoin. The hydrazones that were synthesized are salicylaldehyde salicylic acid hydrazone, benzoin salicylic acid hydrazone, benzil mono hydrazone salicylic acid hydrazone and benzil monoxime salicylic acid hydrazone. These reagents were determined by different methods, IR spectrophotometric determination, the nitrogen content method and melting point determination. These hydrazones act as ligands for determination of some metal ions by making different coloured complexes that were prepared for eight hydrazones with eight metal ions U (VI), Fe (II), Fe (III), Co (II), V (II), Mo (VI), Ni (II) and Cu (II). These complexes were determined by ultraviolet and visible spectrophotometer (UV/VIS) to detect their absorbance and wavelengths (λ max). The two hydrazones salicylaldehyde salicylic acid-hydrazone and benzoin salicylic acid hydrazone, were selected for determination of five metal ions (Fe (II), Fe (III), U (VI), Ni (II) and Cu (II)), using two micelles sodium n-dodecyl sulphate and pyridinium hexa decyl bromide mono hydrate. Their absorbance and wavelengths were detected using UV/VIS spectrophotometer. (Author)

  18. Adhesive and abrasive wear mechanisms in ion implanted metals

    International Nuclear Information System (INIS)

    Dearnaley, G.

    1985-01-01

    The distinction between adhesive and abrasive wear processes was introduced originally by Burwell during the nineteen-fifties, though some authors prefer to classify wear according to whether it is mild or severe. It is argued here that, on the basis of the performance of a variety of ion implanted metal surfaces, exposed to different modes of wear, the Burwell distinction is a valid one which, moreover, enables us to predict under which circumstances a given treatment will perform well. It is shown that, because wear rates under abrasive conditions are very sensitive to the ratio of the hardness of the surface to that of the abrasive particles, large increases in working life are attainable as a result of ion implantation. Under adhesive wear conditions, the wear rate appears to fall inversely as the hardness increases, and it is advantageous to implant species which will create and retain a hard surface oxide or other continuous film in order to reduce metal-metal contact. By the appropriate combination of physico-chemical changes in an implanted layer it has been possible to reduce wear rates by up to three orders of magnitude. Such rates compensate for the shallow depths achievable by ion implantation. (orig.)

  19. Superhydrogels of nanotubes capable of capturing heavy-metal ions.

    Science.gov (United States)

    Song, Shasha; Wang, Haiqiao; Song, Aixin; Hao, Jingcheng

    2014-01-01

    Self-assembly regulated by hydrogen bonds was successfully achieved in the system of lithocholic acid (LCA) mixed with three organic amines, ethanolamine (EA), diethanolamine (DEA), and triethanolamine (TEA), in aqueous solutions. The mixtures of DEA/LCA exhibit supergelation capability and the hydrogels consist of plenty of network nanotubes with uniform diameters of about 60 nm determined by cryogenic TEM. Interestingly, the sample with the same concentration in a system of EA and LCA is a birefringent solution, in which spherical vesicles and can be transformed into nanotubes as the amount of LCA increases. The formation of hydrogels could be driven by the delicate balance of diverse noncovalent interactions, including electrostatic interactions, hydrophobic interactions, steric effects, van der Waals forces, and mainly hydrogen bonds. The mechanism of self-assembly from spherical bilayer vesicles into nanotubes was proposed. The dried hydrogels with nanotubes were explored to exhibit the excellent capability for capturing heavy-metal ions, for example, Cu(2+), Co(2+), Ni(2+), Pb(2+), and Hg(2+). The superhydrogels of nanotubes from the self-assembly of low-molecular-weight gelators mainly regulated by hydrogen bonds used for the removal of heavy-metal ions is simple, green, and high efficiency, and provide a strategic approach to removing heavy-metal ions from industrial sewage. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Spectrophotometric study of some metal ions using some Schiff's bases

    International Nuclear Information System (INIS)

    Elnager, Nawal Mohomed Ibrahim

    2000-05-01

    In this work two schiff bases namely N,N Bis(benzoyl acetone)-o-phenylene diamine (NNBBPD) and N,N Bis(benzoyl acetone)-isopropylene diamine (NNBBAID) were prepared by direct coupling of benzoyl acetone with o-phenylene and isopropylene diamine respectively. The two reagents were identified by IR spectra, thin layer chromatography (TLC) and determination of the percentage of nitrogen contents (N%). It is found that the two reagents form coloured chelates with Fe (II), Fe (III), Cu (II), U (VI), Ni (II) and Co (II). The two reagents were used for the determination of Fe (II), Fe (III) and U (VI). The formulate of these metal ion complexes were obtained using continuous variations, mole ratio and slope ratio methods. Effect of two micelles, namely sodium n-dodecyl sulphate (SDS) and hexadecyl pyridinum broinide monohydrate (HPB) on metal ion complexes were studied. It is found that both of them increase the solubility and the absorbances of the metal ion complexes with variable effects of the absorption maxima. Calibration curves for Fe (II), Fe (II) and U (VI) were obtained in optimum conditions of pH and micelles solutions. (Author)

  1. Modeling the RNA 2'OH activation: possible roles of metal ion and nucleobase as catalysts in self-cleaving ribozymes.

    Science.gov (United States)

    Chval, Zdeněk; Chvalová, Daniela; Leclerc, Fabrice

    2011-09-22

    The RNA 2'OH activation as taking place in the first chemical step of self-cleaving ribozymes is studied theoretically by DFT and MP2 methods using a continuum solvation model (CPCM). The reaction of proton transfer is studied in the presence of two kinds of catalysts: a fully hydrated metal ion (Mg(2+)) or partially hydrated nucleobase (guanine), taken separately or together leading to three different modes of activation. The metal ion is either directly bound (inner-sphere) or indirectly bound (outer-sphere) to the 2'OH group and a hydroxide ion acts as a general or specific base; the nucleobase is taken in anionic or in neutral enol-tautomeric forms playing itself the role of general base. The presence of a close metal ion (outer-sphere) lowers the pK(a) value of the 2'OH group by several log units in both metal-ion and nuleobase catalysis. The direct metal coordination to the 2'OH group (inner-sphere) further stabilizes the developing negative charge on the nucleophile. The switching from the inner-sphere to the outer-sphere coordination appears to be driven by the energy cost for reorganizing the first coordination shell rather than by the electrostatic repulsion between the ligands. The metal-ion catalysis is more effective with a specific base in the dianionic mechanism. On the other hand, the nucleobase catalysis is more effective in the monoanionic mechanism and in the presence of a metal ion acting as a cofactor through nonspecific electrostatic interactions. The results establish a baseline to study the possible roles of metal and nucleobase catalysts and their environment in more realistic models for self-cleaving ribozymes.

  2. Alkylamine functionalized metal-organic frameworks for composite gas separations

    Energy Technology Data Exchange (ETDEWEB)

    Long, Jeffrey R.; McDonald, Thomas M.; D' Alessandro, Deanna M.

    2018-01-09

    Functionalized metal-organic framework adsorbents with ligands containing basic nitrogen groups such as alkylamines and alkyldiamines appended to the metal centers and method of isolating carbon dioxide from a stream of combined gases and carbon dioxide partial pressures below approximately 1 and 1000 mbar. The adsorption material has an isosteric heat of carbon dioxide adsorption of greater than -60 kJ/mol at zero coverage using a dual-site Langmuir model.

  3. Separation of Lead with a Novel Ion Separating Agent Prepared by Clothing a Chitin Whisker on a Potassium Tetratitanate Whisker

    Directory of Open Access Journals (Sweden)

    Juan Liu

    2017-03-01

    Full Text Available Separation of Pb2+ from Cu2+-Pb2+ mixed solution by a newly-developed ion separating agent was examined, which was obtained by clothing chitin whiskers (ChW on the surface of potassium tetratitanate whiskers (PTW. The separation capability and mechanism of the ion separating agent (ChW-PTW was determined, based on the difference of the adsorption isotherm pattern and the adsorption kinetics model between ChW and PTW on Cu2+ and Pb2+, respectively. The results showed that the adsorption process of ChW could be described by Freundlish isotherm. The adsorption affinity of Cu2+ (kF = 0.085·g−1 on ChW was greater than Pb2+ (kF = 0.077 g−1. The adsorption pattern of PTW was inclined to the Langmuir isotherm, and Pb2+ (kL = 310.59 L·mmol−1 could be obviously more easily adsorbed on PTW than Cu2+ (kL = 25.85 L·mmol−1. The experimental data both fitted well with the pseudo-second order kinetics. The reaction rate of Pb2+ (k2 = 4.442 for ChW and k2 = 0.846 for PTW was greater than that of Cu2+ on both ChW and PTW, while the diffusion rate of intra-particles of PTW was much higher than ChW. The adsorption model of ChW and PTW could illustrate well the separation mechanism of ChW-PTW and allowed for relevant results.

  4. Shutdown-functionalized nonwoven separator with improved thermal and electrochemical properties for lithium-ion batteries

    Science.gov (United States)

    Kim, Youngkwon; Lee, Won-Yeol; Kim, Ki Jae; Yu, Ji-Sang; Kim, Young-Jun

    2016-02-01

    A shutdown-functionalized nonwoven separator (SFNS) with improved thermal and electrochemical stabilities is prepared by a simple dip coating method for use in lithium-ion battery (LiB) applications. The SFNS shows thermal stability at 200 °C, while providing shutdown functionality at approximately 140 °C, similar to commercial porous polyethylene separators. The surface-coated polymer prevents leakage current problems and in addition, shows air permeability values similar to that of bare nonwoven separators, while maintaining a thickness of about 20 μm, which is a desired attribute of effective separators for LiBs. The SFNS also shows increased electrolyte uptake and higher conductivity, compared to a bare polyethylene separator. Therefore, a cell with the SFNS exhibits higher discharge capacity and better cycle property than that with a porous polyethylene separator. These results suggest that SFNS is an effective separator for high-performance LiBs.

  5. Isotopic separation through ion cyclotron-resonance: results from the ERIC experiment

    International Nuclear Information System (INIS)

    Compant la Fontaine, A.; Louvet, P.

    1994-01-01

    Stable isotope separation by the means of ion cyclotron-resonance is studied at CEA since 1981. Results from the ERIC experiments are of two types: parameter measurements which help characterizing the plasma and optimizing the process, and isotopic separation results. For example, the selective feature of isotope heating was verified in the cases of zinc and calcium using an electrostatic analyzer. The separation factors of various elements (calcium, zinc, barium, chromium...) are depending on the mass relative difference of the isotopes to be separated, difference which must be large compared to the magnetic field inhomogeneities and the Doppler broadening. 2 figs., 1 tab., 3 refs

  6. Electrospray Ionization Mass Spectrometry: From Cluster Ions to Toxic metal Ions in Biology

    Energy Technology Data Exchange (ETDEWEB)

    Lentz, Nicholas B. [Iowa State Univ., Ames, IA (United States)

    2007-01-01

    This dissertation focused on using electrospray ionization mass spectrometry to study cluster ions and toxic metal ions in biology. In Chapter 2, it was shown that primary, secondary and quarternary amines exhibit different clustering characteristics under identical instrument conditions. Carbon chain length also played a role in cluster ion formation. In Chapters 3 and 4, the effects of solvent types/ratios and various instrumental parameters on cluster ion formation were examined. It was found that instrument interface design also plays a critical role in the cluster ion distribution seen in the mass spectrum. In Chapter 5, ESI-MS was used to investigate toxic metal binding to the [Gln11]-amyloid β-protein fragment (1-16). Pb and Cd bound stronger than Zn, even in the presence of excess Zn. Hg bound weaker than Zn. There are endless options for future work on cluster ions. Any molecule that is poorly ionized in positive ion mode can potentially show an increase in ionization efficiency if an appropriate anion is used to produce a net negative charge. It is possible that drug protein or drug/DNA complexes can also be stabilized by adding counter-ions. This would preserve the solution characteristics of the complex in the gas phase. Once in the gas phase, CID could determine the drug binding location on the biomolecule. There are many research projects regarding toxic metals in biology that have yet to be investigated or even discovered. This is an area of research with an almost endless future because of the changing dynamics of biological systems. What is deemed safe today may show toxic effects in the future. Evolutionary changes in protein structures may render them more susceptible to toxic metal binding. As the understanding of toxicity evolves, so does the demand for new toxic metal research. New instrumentation designs and software make it possible to perform research that could not be done in the past. What was undetectable yesterday will

  7. Simultaneous chirality and enantiomer separation of metallic single-wall carbon nanotubes by gel column chromatography.

    Science.gov (United States)

    Tanaka, Takeshi; Urabe, Yasuko; Hirakawa, Takuya; Kataura, Hiromichi

    2015-09-15

    We report the chirality and enantiomer separation of metallic single-wall carbon nanotubes (SWCNTs) using gel chromatography, which has been the last remaining issue in SWCNT separation that has yet to be achieved. The key to the separation is summarized as the following three points: (i) the use of a preseparated metallic SWCNT mixture to eliminate the semiconducting SWCNTs that are more interactive with the gel; (ii) the reduction of the concentration of dispersant to increase the interaction between the metallic SWCNTs and the gel; and (iii) the use of a long column to increase the number of interaction sites that enhance the slight differences between metallic SWCNT species. Using these three separation conditions, we obtained chirality-sorted metallic SWCNTs, especially (10,4) metallic SWCNTs were highly enriched. Circular dichroism spectra demonstrated the enantiomer separation of metallic SWCNTs. The discrimination of the enantiomers is derived from the dextran in the gel, which is the only enantiomeric moiety in this system. This is the first report on the enantiomer separation of metallic SWCNTs and will contribute to progress in the fundamental physics and applications of SWCNTs.

  8. Application of ion chromatography in the analysis of metals

    International Nuclear Information System (INIS)

    Doepke, T.; Braun, N.; Wuensch, G.

    1992-01-01

    Methods for the determination of chloride in molybdenum, tungsten, niobium and tantalum and of phosphorus in molybdenum and tungsten are presented. After oxidative digestion the analytes are separated from the matrix and accumulated in a small volume of liquid. Unsuppressed ion chromatography serves as the final determination method. The trace-matrix-separation and enrichment of chloride is largely independent of the kind of matrix. The procedure is therefore also applicable to concentrated solutions of various salts. A closed system ensures chloride blanks around 0.2 ppm and detection limits in the higher ppb range. A modification allows an enrichment of bromide and the simultaneous determination of chloride and bromide. (orig.) [de

  9. The momentum-loss achromat - a new method for the isotopical separation of relativistic heavy ions

    International Nuclear Information System (INIS)

    Schmidt, K.H.; Geissel, H.; Muenzenberg, G.; Dufour, J.P.; Hanelt, E.

    1987-03-01

    The application of the slowing-down process of relativistic heavy ions in a layer of matter in ion-optical devices is theoretically investigated. The modifications of the phase space of the ion beam due to the dissipative forces and the straggling phenomena are discussed. Methods are developed to study the properties of the momentum-loss achromat, an isotope separator consisting of an achromatic magnetic system with an energy degrader located in the intermediate dispersive focal plane. This device separates projectile fragments with respect to A and Z up to uranium over a wide energy range with an efficiency in the order of 50% and with separation times of several hundred nanoseconds. (orig.)

  10. Metal negative ion production by a planar magnetron sputter type radio frequency ion source

    Science.gov (United States)

    Yoshioka, K.; Kanda, S.; Kasuya, T.; Wada, M.

    2017-08-01

    A planar magnetron sputter type ion source has been operated to investigate metal negative ion production. Radio frequency power at 13.56 MHz was directly supplied to the planar target made of 2 mm thick Cu disk to maintain plasma discharge and induce DC self-bias to the target for sputtering. Beam profile was obtained and the peak of negative ion beam profile was shifted to 6 mm as the beam traversed the 32 mT magnetic field in the region of the plasma grid. Extraction of Cu- beam was performed and the Cu- beam current was found consisted of two components: Cu-(surface) and Cu-(volume). Negative ion spectra were observed to measure the ratio of the surface component to the volume component. The surface component of Cu- occupied 67% of the total beam at the maximum, while it decreased the fraction down to about 50% as the source pressure was increased.

  11. Structures and physical properties of gaseous metal cationized biological ions.

    Science.gov (United States)

    Burt, Michael B; Fridgen, Travis D

    2012-01-01

    Metal chelation can alter the activity of free biomolecules by modifying their structures or stabilizing higher energy tautomers. In recent years, mass spectrometric techniques have been used to investigate the effects of metal complexation with proteins, nucleobases and nucleotides, where small conformational changes can have significant physiological consequences. In particular, infrared multiple photon dissociation spectroscopy has emerged as an important tool for determining the structure and reactivity of gas-phase ions. Unlike other mass spectrometric approaches, this method is able to directly resolve structural isomers using characteristic vibrational signatures. Other activation and dissociation methods, such as blackbody infrared radiative dissociation or collision-induced dissociation can also reveal information about the thermochemistry and dissociative pathways of these biological ions. This information can then be used to provide information about the structures of the ionic complexes under study. In this article, we review the use of gas-phase techniques in characterizing metal-bound biomolecules. Particular attention will be given to our own contributions, which detail the ability of metal cations to disrupt nucleobase pairs, direct the self-assembly of nucleobase clusters and stabilize non-canonical isomers of amino acids.

  12. Preparation and characterization of a Lithium-ion battery separator from cellulose nanofibers

    Directory of Open Access Journals (Sweden)

    Hongfeng Zhang

    2015-10-01

    Full Text Available Optimizing the desired properties for stretch monolayer separators used in Lithium-ion batteries has been a challenge. In the present study a cellulose nanofiber/PET nonwoven composite separator is successfully fabricated, using a wet-laid nonwoven (papermaking process, which can attain optimal properties in wettability, mechanical strength, thermal resistance, and electrochemical performance simultaneously. The PET nonwoven material, which is fabricated from ultrafine PET fibers by a wet-laid process, is a mechanical support layer. The porous structure of the composite separator was created by cellulose nanofibers coating the PET in a papermaking process. Cellulose nanofibers (CNFs, which are an eco-friendly sustainable resource, have been drawing considerable attention due to their astounding properties, such as: incredible specific surface area, thermal and chemical stability, high mechanical strength and hydrophilicity. The results show that the CNF separator exhibits higher porosity (70% than a PP (polypropylene separator (40%. The CNF separator can also be wetted by electrolyte in a few seconds while a PP separator cannot be entirely wetted after 1 min. The CNF separator has an electrolyte uptake of 250%, while a PP separator has only 65%. Another notable finding is that the CNF separator has almost no shrinkage when exposed to 180 °C for 1 h, whereas a PP separator shrinks by more than 50%. Differential Scanning Calorimetry (DSC shows that the CNF separator has a higher melting point than a PP separator. These findings all indicate that the CNF 29 separator will be more favorable than stretch film for use in Lithium-ion batteries.

  13. Preparation and characterization of a Lithium-ion battery separator from cellulose nanofibers.

    Science.gov (United States)

    Zhang, Hongfeng; Wang, Xiwen; Liang, Yun

    2015-10-01

    Optimizing the desired properties for stretch monolayer separators used in Lithium-ion batteries has been a challenge. In the present study a cellulose nanofiber/PET nonwoven composite separator is successfully fabricated, using a wet-laid nonwoven (papermaking) process, which can attain optimal properties in wettability, mechanical strength, thermal resistance, and electrochemical performance simultaneously. The PET nonwoven material, which is fabricated from ultrafine PET fibers by a wet-laid process, is a mechanical support layer. The porous structure of the composite separator was created by cellulose nanofibers coating the PET in a papermaking process. Cellulose nanofibers (CNFs), which are an eco-friendly sustainable resource, have been drawing considerable attention due to their astounding properties, such as: incredible specific surface area, thermal and chemical stability, high mechanical strength and hydrophilicity. The results show that the CNF separator exhibits higher porosity (70%) than a PP (polypropylene) separator (40%). The CNF separator can also be wetted by electrolyte in a few seconds while a PP separator cannot be entirely wetted after 1 min. The CNF separator has an electrolyte uptake of 250%, while a PP separator has only 65%. Another notable finding is that the CNF separator has almost no shrinkage when exposed to 180 °C for 1 h, whereas a PP separator shrinks by more than 50%. Differential Scanning Calorimetry (DSC) shows that the CNF separator has a higher melting point than a PP separator. These findings all indicate that the CNF 29 separator will be more favorable than stretch film for use in Lithium-ion batteries.

  14. Removal Process of Heavy Metal Ions from Squid Gut Wastes with Dilute Suluric Acid Leaching and Electrowinning Methods

    OpenAIRE

    嶋影, 和宜; 平井, 伸治; 戸田, 茂雄; 山本, 浩

    2003-01-01

    In order to remove heavy metal ions contained in organic squid gut waste, a novel process has been developed with both dilute suluric acid leaching and electrowinning methods. This process was consisted of three procedures, which are the elimination of greasy component in squid gut wastes, the dissolution of heavy metal ions and the electro-deposition of heavy metal ions. Heavy metal ions contained in organic squid gut wastes are zinc, cadmium and copper ions. Heavy metal ions are leached eas...

  15. Extraction of metal ions by neutral β-diphosphoramides

    International Nuclear Information System (INIS)

    Madic, C.

    1990-01-01

    The extracting ability of β-diphosphoramides of the type R-N[P(O)(NMe 2 ) 2 ] 2 with R=-CH 3 (NIPA), -C 12 H 25 (ODIPA), or -C 16 H 33 (OHDIPA) for metal ions such as lanthanides, uranyl, and the transuranium elements Am(III) and Pu(IV) has been studied. Extraction yields depend on the nature of the ligand, the organic diluent (nitromethane, kerosene, tert-butylbenzene), the concentration of nitric acid in the aqueous phase, and the ligand-to-metal ratio, Q. The results show that the bidentate phosphoramides are very efficient extractants for all of the metals studied, even at low ratios Q. The presence of nitric acid generally enhances the extraction yields. On the other hand, selectivity is rather poor with these ligands. A particular effort has been made to determine the nature of extracted species by NMR spectroscopy

  16. Treatment of Copper Converter Flue Dust for the Separation of Metallic/non-metallic Copper by Hydrometallurgical Processing

    OpenAIRE

    Martín, M. I.; López-Delgado, Aurora; López Gómez, Félix Antonio; Gómez Coedo, Aurora; Dorado López, María Teresa; Alguacil, Francisco José

    2003-01-01

    A hydrometallurgical procedure for the separation of copper soluble species from metallic copper of a copper converter flue dust was studied. The high content of metallic copper in the starting material made unique a procedure of such characteristics for the treatment of this secondary copper resource. The procedure consists of leaching and solvent extraction operations. Leaching was carried out under atmospheric conditions using sulphuric acid. Under various experimental conditions the metal...

  17. Self-organized formation of metal-carbon nanostructures by hyperthermal ion deposition

    Energy Technology Data Exchange (ETDEWEB)

    Hannstein, I.K.

    2006-04-26

    The quasi-simultaneous deposition of mass-selected hyperthermal carbon and metal ions results in a variety of interesting film morphologies, depending on the metal used and the deposition conditions. The observed features are of the order of a few nanometres and are therefore interesting for future potential applications in the various fields of nanotechnology. The present study focuses on the structural analysis of amorphous carbon films containing either copper, silver, gold, or iron using amongst others Rutherford Backscattering Spectroscopy, High Resolution Transmission Electron Microscopy, and Energy Dispersive X-Ray Spectroscopy. The film morphologies found are as follows: copper-containing films consist of copper nanoclusters with sizes ranging from about 3 to 9 nm uniformly distributed throughout the amorphous carbon matrix. The cluster size hereby rises with the copper content of the films. The silver containing films decompose into a pure amorphous carbon film with silver agglomerates at the surface. Both, the gold- and the iron-containing films show a multilayer structure of metal-rich layers with higher cluster density separated by metal-depleted amorphous carbon layers. The layer distances are of the order of up to 15 nm in the case of gold-carbon films and 7 nm in the case of iron-carbon films. The formation of theses different structures cannot be treated in the context of conventional self-organization mechanisms basing upon thermal diffusion and equilibrium thermodynamics. Instead, an ion-induced atomic transport, sputtering effects, and the stability of small metal clusters were taken into account in order to model the structure formation processes. A similar multilayer morphology was recently also reported in the literature for metal-carbon films grown by magnetron sputtering techniques. In order to investigate, whether the mechanisms are the same as in the case of the ion beam deposited films described above, first experiments were conducted

  18. Mass Spectrum Analysis of CO2 and N2 Using Ion Beam Separator System

    International Nuclear Information System (INIS)

    Tjipto-Sujitno, BA; Darsono; Agus-Santoso

    2000-01-01

    The main purpose of this research is to study investigate the massspectrum profile of CO 2 and N 2 emitted from Penning ion source using ionbeam separator. Besides that, it is also identified the compositions of CO 2 and N 2 ion gas and their abundances through their mass spectrum profile,because as we know that these ions are consist of ion of atom or molecule aswell as the their abundances. To get these profiles, the ion beam acceleratedin accelerating tube are passed through magnet separator. After passing themagnet separator, the ion current beam was detected using microampere meter.By scanning the strength of magnetic field, it will be found the currentspectrum profile as a function of magnetic field. From this current spectrum,we can make a mass spectrum profile. From experiment done, it was found thatthe mass spectrum peak of CO 2 and N 2 were C + with m/z = (12.00 ± 0.10)amu, O 2 + = (31.96 ± 0.29) amu, CO 2 + = (43.93 ± 0.31) amu, N + (13.97 ± 0.33) amu, and N 2 + = (28.05 ± 0.18) amu. (author)

  19. Separation of uranium from sodium carbonate-sodium bicarbonate eluate by ion exchange method

    International Nuclear Information System (INIS)

    Sakane, Kohji; Hirotsu, Takahiro; Fujii, Ayako; Katoh, Shunsaku; Sugasaka, Kazuhiko

    1982-01-01

    The ion exchange method was used for separating uranium from the eluate (0.5 N Na 2 CO 3 -0.5 N NaHCO 3 ) that was obtained in the extraction process of uranium from natural sea water by using the titanium-activated carbon composite adsorbent. Uranium in the eluate containing 3 mg/l uranium was adsorbed by ion exchange resin (Amberlite IRA-400), and was eluted with the eluent (5% NaCl-0.5% Na 2 CO 3 ). The concentration ratio of uranium in the final concentrated-eluate became more than 20 times. The eluting solution to the adsorbent and the eluant to the resin could be repeatedly used in the desorption-ion exchange process. Sodium carbonate was consumed at the desorption step, and sodium bicarbonate was consumed at the ion exchange step. The concentration ratio of uranium was found to decrease as chloride ion in the eluate increased. (author)

  20. Separation of uranium from sodium carbonate - sodium bicarbonate eluate by ion exchange method

    International Nuclear Information System (INIS)

    Sakane, Kohji; Hirotsu, Takahiro; Fujii, Ayako; Katoh, Shunsaku; Sugasaka, Kazuhiko

    1982-01-01

    The ion exchange method was used for separating uranium from the eluate (0.5 N Na 2 CO 3 -0.5 N NaHCO 3 ) that was obtained in the extraction process of uranium from natural sea water by using the titanium-activated carbon composite adsorbent. Uranium in the eluate containing 3 mg/1 uranium was adsorbed by ion exchange resin (Amberlite IRA-400), and was eluted with the eluant (5 % NaCl-0.5 % Na 2 CO 3 ). The concentration ratio of uranium in the final concentrated-eluate became more than 20 times. The eluting solution to the adsorbent and the eluant to the resin could be repeatedly used in the desorption-ion exchange process. Sodium carbonate was consumed at the desorption step, and sodium bicarbonate was consumed at the ion exchange step. The concentration ratio of uranium was found to decrease as chloride ion in the eluate increased. (author)

  1. Isotherms and thermodynamics for the sorption of heavy metal ions onto functionalized sporopollenin

    Energy Technology Data Exchange (ETDEWEB)

    Gubbuk, Ilkay Hilal, E-mail: ihilalg@gmail.com [Selcuk University, Department of Chemistry, Campus, 42031 Konya (Turkey)

    2011-02-15

    In this study, sporopollenin of Lycopodium clavatum spores was used for the sorption experiment. Glutaraldehyde (GA) immobilized sporopollenin (Sp), is employed as a sorbent in sorption of selected heavy metal ions. The sorbent prepared by sequential treatment of sporopollenin by silanazing compound and glutaraldehyde is suggested for sorption of Cu(II), Zn(II) and Co(II) from aqueous solutions. Experimental conditions for effective sorption of heavy metal ions were optimized with respect to different experimental parameters using batch method in detail. Optimum pH range of Cu(II) has occurred at pH {>=} 5.5 and Zn(II), Co(II) at pH {>=} 5.0, for the batch method. All of the metal ions can be desorbed with 10 cm{sup 3} of 0.5 mol dm{sup -3} of ethylenediaminetetraacetic acid (EDTA) solution. Langmuir, Freundlich and Dubinin-Radushkevich (D-R) isotherm equations were applied to the experimental data. Thermodynamic parameters such as free energy ({Delta}G{sup o}), entropy ({Delta}S{sup o}) and enthalpy ({Delta}H{sup o}) were also calculated from the sorption results used to explain the mechanism of the sorption. The results indicated that this sorbent is successfully employed in the separation of trace Cu(II), Zn(II) and Co(II) from the aqueous solutions.

  2. Solid NMR study of lithium ions accommodated in various transition metal oxides

    International Nuclear Information System (INIS)

    Kanzaki, Yasushi; Suzuki, Noriko

    2008-01-01

    Solid NMR was used to elucidate the lithium accommodation/extraction reaction in various transition metal oxides. The first study was the lithium ion exchange reaction of titanium antimonic acid (TiSbA). The effect of hydration on the selectivity of lithium ion in the solid phase was examined using 7 Li NMR. The second study was the irreversible ion exchange behavior of HNbO 3 . The selectivity for the lithium ion and the irreversible behavior were examined using 1 H and 7 Li NMR. The third study was the isotope separation between 6 Li and 7 Li in various inorganic ion exchangers. The high isotope separation coefficient was ascribed to the degree of dehydration during the ion exchange reaction. The degree of dehydration was examined by 1 H and 7 Li NMR studies. The last study was determining the mechanism of the lithium accommodation/extraction reaction of λ-MnO 2 in an aqueous solution. The different paths between the accommodation and extraction and the formation of MnO 4- during the accommodation were determined by chemical analysis. The Knight shift in the 7 Li MAS-NMR spectra of Li 0.5 MnO 2 suggested the localization of the electron density on the lithium nuclei. An XPS study also suggested the presence of an electron density on the lithium nuclei. A pH-independent redox couple was assumed to account for the accommodation/extraction reaction of lithium ions, such as Li(I)/Li(0). (author)

  3. Sequestering Potential of Peach Nut Shells as an Efficient Sorbent for Sequestering Some Toxic Metal Ions from Aqueous Waste: A Kinetic and Thermodynamic Study

    OpenAIRE

    Muhammad Ashraf Shaheen; Rehana Akram; Abdul Karim; Tahir Mehmood; Robina Farooq; Mudassir Iqbal

    2016-01-01

    The peach nut shells potential as a low cost biosorbent for separation of certain metal ions from aqueous media was investigated. The effects of different parameters such as pH, shaking speed, initial metal ions concentration and their contact time with adsorbent on sorption efficiency of biosorbent was investigated to optimize the parameters for maximum sorption. The FT–IR spectroscopy and TGA were used to characterize the biosorbent. A significant increase in sorption was noted with rise i...

  4. Heavy metal ions adsorption from mine waters by sawdust

    Directory of Open Access Journals (Sweden)

    G. Bogdanović

    2009-10-01

    Full Text Available In this work the results on the batch and column adsorption of copper and some associated ions by employing linden and poplar sawdust as a low-cost adsorbent are presented. The mine water from a local abandoned copper mine, as well as synthetic solutions of those ions which are the main constituents of the mine water were both used as a model-system in this study. The adsorption ability of the chosen sawdust to adsorb heavy metal ions is considered as a function of the initial pH of the solution and kind of metal ions. At lower pH of solutions the adsorption percentage (AD % decreases leading to a zero AD % at pH < 1.1. Maximum AD % is achieved at 3.5 < pH < 5. It was found that poplar and linden sawdust have both almost equal adsorption capacities against copper ions. The highest AD % ( ≈80% was achieved for Cu2+, while for Fe2+ it was slightly above 10%. The other considered ions (Zn2+ and Mn2+ were within this interval. The results obtained in the batch mode were verified through the column test by using the real mine water originating from an acid mine drainage (AMD of the copper mine „Cerovo“, RTB Bor. The breakthrough curves are presented as a function of the aqueous phase volume passed through the column allowing having an insight into the column adsorption features. Breakthrough points were determined for copper, manganese and zinc ions. A very high adsorption degree – higher than 99% was achieved in these experiments for all mentioned ions. After completing the adsorption, instead of desorption, the loaded sawdust was drained, dried and burned; the copper bearing ash was then leached with a controlled volume of sulphuric acid solution to concentrate copper therein. The obtained leach solution had the concentration of copper higher than 15 g dm-3 and the amount of H2SO4 high enough to serve as a supporting electrolyte suitable to be treated by the electrowinning for recovery of copper. The technology process based on the column

  5. INSTRUMENTS AND METHODS OF INVESTIGATION: Plasma isotope separation based on ion cyclotron resonance

    Science.gov (United States)

    Dolgolenko, Dmitrii A.; Muromkin, Yurii A.

    2009-04-01

    Experiments that have been conducted in the USA, France, and Russia to investigate isotopically selective ion cyclotron resonance (ICR) as a tool for plasma isotope separation are analyzed. Because this method runs into difficulties at low values of the relative isotope mass difference ΔM/M, for some elements (for gadolinium, as an example) isotope separation still remains a problem. There are ways to solve it, however, as experimental results and theoretical calculations suggest.

  6. Application of vacuum metallurgy to separate pure metal from mixed metallic particles of crushed waste printed circuit board scraps.

    Science.gov (United States)

    Zhan, Lu; Xu, Zhenming

    2008-10-15

    The principle of separating pure metal from mixed metallic particles (MMPs) byvacuum metallurgy is that the vapor pressures of various metals at the same temperature are different As a result, the metal with high vapor pressure and low boiling point can be separated from the mixed metals through distillation or sublimation, and then it can be recycled through condensation under a certain condition. The vacuum metallurgy separation (VMS) of MMPs of crushed waste printed circuit boards (WPCBs) has been studied in this paper. Theoretical analyses show that the MMPs (copper, zinc, bismuth, lead, and indium, for example) can be separated by vacuum metallurgy. The copper particles (0.15-0.20 mm) and zinc particles (<0.30 mm) were chosen to simulate the MMPs of crushed WPCBs. Experimental results show that the separated efficiency of zinc in the copper-rich particles achieves 96.19 wt % when the vacuum pressure is 0.01-0.10 Pa, the heating temperature is 1123 K, and the heating time is 105 min. Under this operation condition, the separated efficiency of zinc in the copper-rich particles from crushed WPCBs achieves 97.00 wt % and the copper purity increases from 90.68 to 99.84 wt %.

  7. Stability of Polymeric Separators in Lithium Metal Batteries in a Low Voltage Environment

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xing; Tao, Jinhui; Hu, Dehong; Engelhard, Mark H.; Zhao, Wengao; Zhang, Jiguang; Xu, Wu

    2018-03-20

    The separator is an important component in rechargeable lithium (Li) metal batteries, however, less attention has been focused on it. In this work, several representative separators, such as polyethylene, polypropylene, and such polyolefin separators with coatings of ceramic and polymeric materials, were selected to assemble into Li||Cu and Li||Li coin cells to test the Coulombic efficiency values of Li metal and the cycling stability in a low voltage environment less than 1 V. Moreover, two representative electrolytes of LiPF6 and LiTFSI-LiBOB in carbonate solvent mixture were also employed to systematically study their interactions with the separators in Li metal cells. It was found that the separators could largely affect the Coulombic efficiency values and cycling stability of Li metal cells, especially when using the LiPF6 electrolyte, which is probably due to the effect of the trace amount of HF in the LiPF6 electrolyte. Among these separators, polyethylene separator is the most stable one with Li metal. This work gave some reasonable explanations for the above phenomena, which could provide references for Li metal battery studies when employing Li||Cu and Li||Li cells conducted in the low voltage environment.

  8. [Metal ions restrain the elimination of 4-tert-octylphenol by delta-MnO2].

    Science.gov (United States)

    Li, Fei-Li; Mou, Hua-Qian

    2013-06-01

    The effect of metal ions on elimination of 4-t-OP by synthetic delta-MnO2 suspension at pH 4.0 was studied. Experiments indicated that the removal of 4-t-OP by delta-MnO2 achieved 100% at reaction time of 150 min. However, the removal of 4-t-OP by delta-MnO2 was restrained when metal ions were added, and the higher concentration of metal ion was, the stronger the inhibition produced. Additionally, there were apparent differences among the inhibitory effect of the tested metal ions. Firstly, Pb2+ and Mn2+ had the strongest effect at pH 4.0, followed by the transition metal ions, then the alkaline earth ions, while the alkali metal ions had little influence on the removal of 4-t-OP by delta-MnO2. Also comparing the adsorption results of metal ions by delta-MnO2, Pb2+ showed the greatest attraction with delta-MnO2, and among the other metal ions, transition metal ions were adsorbed a little more strongly on delta-MnO2 than alkaline earth metal ions. Consequences showed that the inhibitory effects of metal ions were due to their occupying reactive sites on delta-MnO2 surface, which competed with 4-t-OP. Moreover, the dissimilar suppressions were contributed by the different adsorption capacities, surface structure change of MnO2 and the difference of free metal ion percentage in solution as well as metal ions radii.

  9. Electrodialytic Separation of Phosphorus and Heavy Metals from Two Types of Sewage Sludge Ash

    DEFF Research Database (Denmark)

    Ottosen, Lisbeth M.; Jensen, Pernille Erland; Kirkelund, Gunvor Marie

    2014-01-01

    During sewage sludge incineration phosphorus (P) is retained in the ash in a form not directly available to plants. As P is a sparse resource, it is important to develop techniques for recovery of P from incinerated sewage sludge ashes (ISSA). Heavy metals are concentrated in ISSA and separation....... The separation method was best suited for the Fe-rich ash, where it was possible to separate P into one processing solution, heavy metals (Cu, Zn, Ni, Pb) into another, keeping the ash suspended in a third solution (which though still contained P after 1 week of EDS). For the Al rich ash, the separation...

  10. Polymethylmethacrylate/Polyacrylonitrile Membranes via Centrifugal Spinning as Separator in Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Meltem Yanilmaz

    2015-04-01

    Full Text Available Electrospun nanofiber membranes have been extensively studied as separators in Li-ion batteries due to their large porosity, unique pore structure, and high electrolyte uptake. However, the electrospinning process has some serious drawbacks, such as low spinning rate and high production cost. The centrifugal spinning technique can be used as a fast, cost-effective and safe technique to fabricate high-performance fiber-based separators. In this work, polymethylmethacrylate (PMMA/polyacrylonitrile (PAN membranes with different blend ratios were produced via centrifugal spinning and characterized by using different electrochemical techniques for use as separators in Li-ion batteries. Compared with commercial microporous polyolefin membrane, centrifugally-spun PMMA/PAN membranes had larger ionic conductivity, higher electrochemical oxidation limit, and lower interfacial resistance with lithium. Centrifugally-spun PMMA/PAN membrane separators were assembled into Li/LiFePO4 cells and these cells delivered high capacities and exhibited good cycling performance at room temperature. In addition, cells using centrifugally-spun PMMA/PAN membrane separators showed superior C-rate performance compared to those using microporous polypropylene (PP membranes. It is, therefore, demonstrated that centrifugally-spun PMMA/PAN membranes are promising separator candidate for high-performance Li-ion batteries.

  11. Electrospun polyacrylonitrile/polyurethane composite nanofibrous separator with electrochemical performance for high power lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zainab, Ghazala [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Wang, Xianfeng, E-mail: wxf@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Key Laboratory of High Performance Fibers & Products, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Nanofibers Research Center, Modern Textile Institute, Donghua University, Shanghai 200051 (China); Yu, Jianyong [Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Key Laboratory of High Performance Fibers & Products, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Nanofibers Research Center, Modern Textile Institute, Donghua University, Shanghai 200051 (China); Zhai, Yunyun; Ahmed Babar, Aijaz; Xiao, Ke [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Ding, Bin, E-mail: binding@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Key Laboratory of Textile Science & Technology, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Key Laboratory of High Performance Fibers & Products, Ministry of Education, College of Textiles, Donghua University, Shanghai 201620 (China); Nanofibers Research Center, Modern Textile Institute, Donghua University, Shanghai 200051 (China)

    2016-10-01

    Lithium ion batteries (LIBs) for high performance require separators with auspicious reliability and safety. Keeping LIBs reliability and safety in view, microporous polyacrylonitrile (PAN)/polyurethane (PU) nonwoven composite separator have been developed by electrospinning technique. The physical, electrochemical and thermal properties of the PAN/PU separator were characterized. Improved ionic conductivity up to 2.07 S cm{sup −1}, high mechanical strength (10.38 MPa) and good anodic stability up to 5.10 V are key outcomes of resultant membranes. Additionally, high thermal stability displaying only 4% dimensional change after 0.5 h long exposure to 170 °C in an oven, which could be valuable addition towards the safety of LIBs. Comparing to commercialized polypropylene based separators, resulting membranes offered improved internal short-circuit protection function, offering better rate capability and enhanced capacity retention under same observation conditions. These fascinating characteristics endow these renewable composite nonwovens as promising separators for high power LIBs battery. - Highlights: • The PAN/PU based separators were prepared by multi-needle electrospinning technique. • The electrospun separators displays good mechanical properties and thermal stability. • These separators exhibit good wettability with liquid electrolyte, high ion conductivity and internal short-circuit protection. • Nanofibrous composite nonwoven possesses stable cyclic performance which give rise to acceptable battery performances.

  12. Electrospun polyacrylonitrile/polyurethane composite nanofibrous separator with electrochemical performance for high power lithium ion batteries

    International Nuclear Information System (INIS)

    Zainab, Ghazala; Wang, Xianfeng; Yu, Jianyong; Zhai, Yunyun; Ahmed Babar, Aijaz; Xiao, Ke; Ding, Bin

    2016-01-01

    Lithium ion batteries (LIBs) for high performance require separators with auspicious reliability and safety. Keeping LIBs reliability and safety in view, microporous polyacrylonitrile (PAN)/polyurethane (PU) nonwoven composite separator have been developed by electrospinning technique. The physical, electrochemical and thermal properties of the PAN/PU separator were characterized. Improved ionic conductivity up to 2.07 S cm −1 , high mechanical strength (10.38 MPa) and good anodic stability up to 5.10 V are key outcomes of resultant membranes. Additionally, high thermal stability displaying only 4% dimensional change after 0.5 h long exposure to 170 °C in an oven, which could be valuable addition towards the safety of LIBs. Comparing to commercialized polypropylene based separators, resulting membranes offered improved internal short-circuit protection function, offering better rate capability and enhanced capacity retention under same observation conditions. These fascinating characteristics endow these renewable composite nonwovens as promising separators for high power LIBs battery. - Highlights: • The PAN/PU based separators were prepared by multi-needle electrospinning technique. • The electrospun separators displays good mechanical properties and thermal stability. • These separators exhibit good wettability with liquid electrolyte, high ion conductivity and internal short-circuit protection. • Nanofibrous composite nonwoven possesses stable cyclic performance which give rise to acceptable battery performances.

  13. Liquid-liquid extraction of divalent transition metal ions with a novel bis-β-ketoester extraction reagent.

    Science.gov (United States)

    Ohmuro, Satoshi; Kishi, Hiromasa; Yoshihara, Nobutoshi; Kokusen, Hisao

    2014-10-01

    Solvent extraction is a very effective method for the separation of metal ions. N,N'-bis(2-hydroxy-phenylmethyl)-N,N'-bis(2-pyridylmetyl)-1,2-ethanediamine derivatives have been researched for solvent extraction of metal ions. In this study. We synthesized a bis-β-ketoester ligand and evaluated its selectivity in extracting divalent transition metal ions. The ligand, hexane-1,6-diyl bis (4,4,4-trifluoro-3-oxobutanoate) (H2hdfob or H2L) was synthesized in one step by transesterification of ethyl 4,4,4-trifluoroacetoacetate with 1,6-hexanediol. The multidentate ligand H2hdfob successfully extracted divalent transition metal ions into its organic phase. The relationship between logD, which is a distribution ratio (D), and pH or log[H2L]o exhibited linear relationships with slopes of approximately +2 and +1, respectively. Based on these results, we proposed a mechanism of extraction with H2hdfob. Extraction with tetradentate H2hdfob provides a new method for enhancing selectivity of divalent metal ions, in comparison to other bidentate ligands. Copyright © 2014 Elsevier B.V. All rights reserved.

  14. Adsorption Equilibrium for Heavy Metal Divalent Ions (Cu2+, Zn2+, and Cd2+ into Zirconium-Based Ferromagnetic Sorbent

    Directory of Open Access Journals (Sweden)

    Agnes Yung Weng Lee

    2017-01-01

    Full Text Available Zirconium-based ferromagnetic sorbent was fabricated by coprecipitation of Fe2+/Fe3+ salts in a zirconium solution and explored as a potential sorbent for removing the Cu2+, Zn2+, and Cd2+ from aqueous solution. The sorbent could easily be separated from aqueous solution under the influence of external magnetic field due to the ferromagnetism property. A trimodal distribution was obtained for the sorbent with average particle size of 22.74 μm. The –OH functional groups played an important role for efficient removal of divalent ions. The surface of the sorbent was rough with abundant protuberance while the existence of divalent ions on the sorbent surface after the sorption process was demonstrated. Decontamination of the heavy metal ions was studied as a function of initial metal ions concentration and solution pH. Uptake of the heavy metal ions showed a pH-dependent profile with maximum sorption at around pH 5. The presence of the ferromagnetic sorbent in solution at different initial pH has shown a buffering effect. Equilibrium isotherms were analyzed using Langmuir, Freundlich, Dubinin-Radushkevich, and Temkin isotherm models. Adequacy of fit for the isotherm models based on evaluation of R2 and ARE has revealed that heavy metal ions decontamination was fitted well with the Freundlich model.

  15. Solvent extraction of lanthanoid, yttrium and some polyvalent metal ions with phosphoric acid esters of Triton X-100

    International Nuclear Information System (INIS)

    Yoshida, Isao; Hirasawa, Jun'ichi; Tsumagari, Hiroto; Ueno, Keihei; Takagi, Makoto.

    1986-01-01

    Polyoxyethylene chain-containing nonionic surfactant, Triton X-100 (decaethyleneglycol mono(4-(1,1,3,3-tetramethylbutyl)phenyl) ether; ROH) was derived to phosphate mono-, di-, and tri-esters RH 2 PO 4 , R 2 HPO 4 and R 3 PO 4 ; abbreviated as MTP, DTP and TTP, respectively) and the metal extraction behavior of these phosphate esters was studied in 1,2-dichloroethane-water system with particular emphasis on lanthanoid(III), yttrium(III), and some other polyvalent metal ions. The extraction was carried out at pH 2 in the presence (for TTP) or in the absence (for MTP and DTP) of picric acid. The metal extraction ability of these extractants followed the order of MTP > DTP > TTP under these extraction conditions. In the extraction by MTP and DTP, the extractability of lanthanoid ions increased with the increase in their atomic number. Mean separation factor of thirteen pairs of adjacent lanthanoids was evaluated to be 1.7 for MTP and 1.4 for DTP. On the other hand, the corresponding values for TTP was almost unity. None of these compounds practically extracted other polyvalent metal ions except iron ion. Iron(III) ion was extracted with MTP and with DTP to a similar level to those of lanthanoid ions. (author)

  16. Hydration to the poly(oxyethylene) derivative complexes of alkali metal ions and barium ion in 1,2-dichloroethane

    International Nuclear Information System (INIS)

    Kikuchi, Yoichi; Kubota, Mitsuru; Suzuki, Toshio; Sawada, Kiyoshi.

    1994-01-01

    A series of poly(oxyethylene) derivatives (POE compound) complexes of alkali metal and barium ions were extracted into 1,2-dichloroethane (1,2-DCE) by forming ion-pairs with picrate ion. Water molecules were coextracted into 1,2-DCE with the ion-pairs. The mean number of water molecules bound to the POE compound, X H2O,S , and its complex, X H2O,comp , in water saturated with 1,2-DCE was determined by means of aquametry. The X H2O,S value increases with the increase in the number of the oxyethylene units (EO unit) of the POE compound. The X H2O,comp value decreases in the order Li + >Na + >K + ≅Rb + ≅Cs + in any POE compound systems, and increases with the number of EO units of the POE compounds for a given metal ion. These results are interpreted by the hypothesis that the water molecules bound to the complex are those hydrated to the central metal ion, and the hydrated metal ion is surrounded by the EO chain with a helical conformation in the complex. The large number of water molecules are coordinating to the lithium ion complexes and bring about a serious distortion in the helical structure of the complexes. Because of the ion-pair formation with two picrate ions, the X H2O,comp values of barium ion complexes are smaller than those of potassium ion complexes. (author)

  17. Hydration number of alkali metal ions determined by insertion in a conducting polymer

    DEFF Research Database (Denmark)

    Skaarup, Steen

    2008-01-01

    In aqueous solutions, the alkali metals ions are associated with a number of H2O molecules. A distinction is made between a primary solvent shell, (or inner solvation shell), consisting of H2O molecules directly coordinated to the metal ion, and a secondary (or outer) solvation shell, consisting....... The solvation of alkali metal ions has been discussed for many years without a clear consensus. This work presents a systematic study of the hydration numbers of the 5 alkali metal ions, using the electrochemical insertion of the ions in a conducting polymer (polypyrrole containing the large immobile anion DBS...

  18. Adsorption of Heavy Metal Ions from Aqueous Solutions by Bentonite Nanocomposites.

    Science.gov (United States)

    Ma, Jing; Su, Guojun; Zhang, Xueping; Huang, Wen

    2016-08-01

    A series of bentonite nanocomposites have been synthesized by modifying bentonite with hexadecyltrimethylammonium bromide (CTMAB) and the common complexing agents, complexone (ethylene diamine tetraacetic acid, EDTA) or mercaptocomplexant (2-Mercaptobenzothiazole, MBT). These adsorbents are used to remove heavy metal ions (Cu(2+), Zn(2+), Mn(2+),Co(2+)). The Bent-CTMAB-MBT adsorbed metal ions are higher than Bent-CTMAB-EDTA under the same ion concentration in AAS. Compared with the single ion system, the adsorption of the mixed ion system of Cu(2+), Zn(2+), Mn(2+), Co(2+) had decreased differently. In the mixed system, the adsorption of Mn(2+) is significantly lower, but the adsorption of Cu(2+) was highest. The adsorption sequence of these four metal ions was Cu(2+) > Zn(2+) > Co(2+) > Mn(2+), and the selective adsorption was closely related to the hydration energy of heavy metal ions. We could remove more metal ions in different stages with the adsorption sequence.

  19. New Catalytic DNA Biosensors for Radionuclides and Metal ions

    International Nuclear Information System (INIS)

    Lu, Yi

    2003-01-01

    The goals of the project are to develop new catalytic DNA biosensors for simultaneous detection and quantification of bioavailable radionuclides and metal ions, and apply the sensors for on-site, real-time assessment of concentration, speciation and stability of the individual contaminants during and after bioremediation. A negative selection strategy was tested and validated. In vitro selection was shown to yield highly active and specific transition metal ion-dependent catalytic DNA/RNA. A fluorescence resonance energy transfer (FRET) study of in vitro selected DNA demonstrated that the trifluorophore labeled system is a simple and powerful tool in studying complex biomolecules structure and dynamics, and is capable of revealing new sophisticated structural changes. New fluorophore/quenchers in a single fluorosensor yielded improved signal to noise ratio in detection, identification and quantification of metal contaminants. Catalytic DNA fluorescent and colorimetric sensors were shown useful in sensing lead in lake water and in leaded paint. Project results were described in two papers and two patents, and won an international prize

  20. The effect of copper ions, aluminium ions and their mixtures on separation of pectin from the sugar beet juice

    Directory of Open Access Journals (Sweden)

    Kuljanin Tatjana A.

    2013-01-01

    Full Text Available In sugar industry there is a problem of the presence of undesirable macromolecules compounds such as pectin in sugar beet juice. The affinity of calcium ions commonly used in the sugar industry for the removal of pectin from the sugar beet juice is relatively small. Coagulation and precipitation of pectin can be performed by process of discharging that is chemically induced. Compounds with di- and trivalent cations such as pure CuSO4, Al2(SO43 or their mixtures can be applied for clarification of pectin colloidal systems. According to data from the order of pectin selectivity to divalent metal ions, Cu2+ ions are the first order of ion binding. Also, aluminum sulfate is commonly used in the waste water treatment. Two model solutions of pectin whose concentration corresponds to the concentration of these macromolecules in sugar beet juice (0.1% w/w are investigated. Using a method of measuring zeta potential, it was proven for both investigated pectin that fewer quantities of Cu2+ ions compared to the values of Al3+ ions are needed to reach zero zeta potential. In all the investigated coagulants and their mixtures, zeta potential has changed the sign. In experiments with mixtures has been shown that pure salts showed better coagulation properties. The reduced strength of binding of cations in the case of most of the applied mixture of Cu2+ and Al3+ ions, can be explained by the mutual competition of these ions for the adsorption site (COO- groups on the surface of macromolecules. Mixture with approximately equal shares of ions Cu2+ and Al3+ had the most unfavorable coagulation ability (ion antagonism. Mechanism of discharge as well as the model of double electric layer surrounding pectin macromolecules in the presence of mixtures of Cu2+ and Al3+ ions are suggested. However, due to possible undesirable effects of CuSO4 on food processing, Al2(SO43 is proposed instead of traditional coagulant CaO, not only because of lower consumptions of

  1. Ion chromatography with the indirect ultraviolet detection of alkali metal ions and ammonium using imidazolium ionic liquid as ultraviolet absorption reagent and eluent.

    Science.gov (United States)

    Liu, Yong-Qiang; Yu, Hong

    2016-08-01

    Indirect ultraviolet detection was conducted in ultraviolet-absorption-agent-added mobile phase to complete the detection of the absence of ultraviolet absorption functional group in analytes. Compared with precolumn derivatization or postcolumn derivatization, this method can be widely used, has the advantages of simple operation and good linear relationship. Chromatographic separation of Li(+) , Na(+) , K(+) , and NH4 (+) was performed on a carboxylic acid base cation exchange column using imidazolium ionic liquid/acid/organic solvent as the mobile phase, in which imidazolium ionic liquids acted as ultraviolet absorption reagent and eluting agent. The retention behaviors of four kinds of cations are discussed, and the mechanism of separation and detection are described. The main factors influencing the separation and detection were the background ultraviolet absorption reagent and the concentration of hydrogen ion in the ion chromatography-indirect ultraviolet detection. The successful separation and detection of Li(+) , Na(+) , K(+) , and NH4 (+) within 13 min was achieved using the selected chromatographic conditions, and the detection limits (S/N = 3) were 0.02, 0.11, 0.30, and 0.06 mg/L, respectively. A new separation and analysis method of alkali metal ions and ammonium by ion chromatography with indirect ultraviolet detection method was developed, and the application range of ionic liquid was expanded. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Gas/vapour separation using ultra-microporous metal-organic frameworks: insights into the structure/separation relationship.

    Science.gov (United States)

    Adil, Karim; Belmabkhout, Youssef; Pillai, Renjith S; Cadiau, Amandine; Bhatt, Prashant M; Assen, Ayalew H; Maurin, Guillaume; Eddaoudi, Mohamed

    2017-06-06

    The separation of related molecules with similar physical/chemical properties is of prime industrial importance and practically entails a substantial energy penalty, typically necessitating the operation of energy-demanding low temperature fractional distillation techniques. Certainly research efforts, in academia and industry alike, are ongoing with the main aim to develop advanced functional porous materials to be adopted as adsorbents for the effective and energy-efficient separation of various important commodities. Of special interest is the subclass of metal-organic frameworks (MOFs) with pore aperture sizes below 5-7 Å, namely ultra-microporous MOFs, which in contrast to conventional zeolites and activated carbons show great prospects for addressing key challenges in separations pertaining to energy and environmental sustainability, specifically materials for carbon capture and separation of olefin/paraffin, acetylene/ethylene, linear/branched alkanes, xenon/krypton, etc. In this tutorial review we discuss the latest developments in ultra-microporous MOF adsorbents and their use as separating agents via thermodynamics and/or kinetics and molecular sieving. Appreciably, we provide insights into the distinct microscopic mechanisms governing the resultant separation performances, and suggest a plausible correlation between the inherent structural features/topology of MOFs and the associated gas/vapour separation performance.

  3. Endonuclease active site plasticity allows DNA cleavage with diverse alkaline Earth and transition metal ions.

    Science.gov (United States)

    Vasu, Kommireddy; Saravanan, Matheshwaran; Nagaraja, Valakunja

    2011-09-16

    A majority of enzymes show a high degree of specificity toward a particular metal ion in their catalytic reaction. However, Type II restriction endonuclease (REase) R.KpnI, which is the first member of the HNH superfamily of REases, exhibits extraordinary diversity in metal ion dependent DNA cleavage. Several alkaline earth and transition group metal ions induce high fidelity and promiscuous cleavage or inhibition depending upon their concentration. The metal ions having different ionic radii and co-ordination geometries readily replace each other from the enzyme's active site, revealing its plasticity. Ability of R.KpnI to cleave DNA with both alkaline earth and transition group metal ions having varied ionic radii could imply utilization of different catalytic site(s). However, mutation of the invariant His residue of the HNH motif caused abolition of the enzyme activity with all of the cofactors, indicating that the enzyme follows a single metal ion catalytic mechanism for DNA cleavage. Indispensability of His in nucleophile activation together with broad cofactor tolerance of the enzyme indicates electrostatic stabilization function of metal ions during catalysis. Nevertheless, a second metal ion is recruited at higher concentrations to either induce promiscuity or inhibit the DNA cleavage. Regulation of the endonuclease activity and fidelity by a second metal ion binding is a unique feature of R.KpnI among REases and HNH nucleases. The active site plasticity of R.KpnI opens up avenues for redesigning cofactor specificities and generation of mutants specific to a particular metal ion.

  4. The Effect of Complex Formation upon the Redox Potentials of Metallic Ions. Cyclic Voltammetry Experiments.

    Science.gov (United States)

    Ibanez, Jorge G.; And Others

    1988-01-01

    Describes experiments in which students prepare in situ soluble complexes of metal ions with different ligands and observe and estimate the change in formal potential that the ion undergoes upon complexation. Discusses student formation and analysis of soluble complexes of two different metal ions with the same ligand. (CW)

  5. Encapsulation of Metal Cations by the PhePhe Ligand: A Cation-pi Ion Cage

    NARCIS (Netherlands)

    Dunbar, R. C.; Steill, J. D.; Oomens, J.

    2011-01-01

    Structures and binding thermochemistry are investigated for protonated PhePhe and for complexes of PhePhe with the alkaline-earth ions Ba2+ and Ca2+, the alkali-metal ions Li+, Na+, K+, and Cs+, and the transition-metal ion Ag+. The two neighboring aromatic side chains open the possibility of a

  6. Chirality-induced conformational preferences in peptide-metal ion binding revealed by IR spectroscopy

    NARCIS (Netherlands)

    Dunbar, R.C.; Steill, J.D.; Oomens, J.

    2011-01-01

    Chirality reversal of a residue in a peptide can change its mode of binding to a metal ion, as shown here experimentally by gas-phase IR spectroscopy of peptide−metal ion complexes. The binding conformations of Li+, Na+, and H+ with the ll and dl stereoisomers of PhePhe were compared through IR ion

  7. Chirality-Induced Conformational Preferences in Peptide-Metal Ion Binding Revealed by IR Spectroscopy

    NARCIS (Netherlands)

    Dunbar, R. C.; Steill, J. D.; Oomens, J.

    2011-01-01

    Chirality reversal of a residue in a peptide can change its mode of binding to a metal ion, as shown here experimentally by gas-phase IR spectroscopy of peptide metal ion complexes. The binding conformations of Li+, Na+, and H+ with the LL and DL stereoisomers of PhePhe were compared through IR ion

  8. Encapsulation of metal cations by the PhePhe ligand: a cation-pi ion cage

    NARCIS (Netherlands)

    Dunbar, R.C.; Steill, J.D.; Oomens, J.

    2011-01-01

    Structures and binding thermochemistry are investigated for protonated PhePhe and for complexes of PhePhe with the alkaline-earth ions Ba2+ and Ca2+, the alkali-metal ions Li+, Na+, K+, and Cs+, and the transition-metal ion Ag+. The two neighboring aromatic side chains open the possibility of a

  9. Synthesis of Anomeric Methyl Fructofuranosides and Their Separation on an Ion-Exchange Resin

    Science.gov (United States)

    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.

  10. Kinetics of Cu (II) separation by ion flotation techniques, in cells with flexible spargers

    International Nuclear Information System (INIS)

    Reyes, M.; Tavera, F. J.; Escudero, R.; Patino, F.; Salinas, E.; Rivera, I.

    2010-01-01

    This research studies and experimentally determines the kinetic parameters and effect of modifying the hydrodynamics and chemical conditions of the air-liquid dispersions during the Cu (II) extraction by ion flotation techniques in cells with porous spargers. Results show that the elimination of Cu (II) from solution can be carried out by ion flotation in one stage, obtaining efficiencies of 68% and 56% for the flat and cylindrical sparger respectively with a xanthate concentration of 0,02 g/l. In multistage systems five cells, recoveries over 92 % were achieved for both sparger geometries. The behavior of the flotation apparent kinetic constant is linear to the parameters that characterize dispersion (Jg, eg y Db), until a point is achieved where the process instability makes the system inoperable. The results show that removing base metal ions by ion flotation is strongly affected by the following factors: collector concentration [C], Jg, eg, Db, Jl and Sb. (Author) 20 refs

  11. Modification of solid surface by intense pulsed light-ion and metal-ion beams

    Science.gov (United States)

    Nakagawa, Y.; Ariyoshi, T.; Hanjo, H.; Tsutsumi, S.; Fujii, Y.; Itami, M.; Okamoto, A.; Ogawa, S.; Hamada, T.; Fukumaru, F.

    1989-03-01

    Metal surfaces of Al, stainless-steel and Ti were bombarded with focused intense pulsed proton and carbon ion beams (energy ˜ 80 keV, current density ≲ 1000 A/cm 2, pulse width ˜ 300 ns). Thin titanium carbide layers were produced by carbon-ion irradiation on the titanium surface. The observed molten surface structures and recrystallized layer (20 μm depth) indicated that the surfaces reached high temperatures as a result of the irradiation. The implantation of intense pulsed metal ion beams (Al +, ˜ 20 A/cm 2) with simultaneous deposition of anode metal vapor on Ti and Fe made a mixed layer of AlTi and AlFe of about 0.5 μm depth. Ti and B multilayered films evaporated on glass substrates were irradiated by intense pulsed proton beams of relatively lower current density (10-200 A/cm 2). Ti films containing B atoms above 10 at.% were obtained. When the current density was about 200 A/cm 2 diffraction peaks of TiB 2 appeared.

  12. Formation of negative ions on a metal surface

    International Nuclear Information System (INIS)

    Amersfoort, P.W. van.

    1987-01-01

    In this thesis a fundamental study of the charge exchange process of positive ions on the converter surface is presented. Beams of hydrogen ad cesium ions are scattered from a thoroughly cleaned W(110) surface, under ultra-high vacuum conditions. The cesium coverage of the surface is a controlled parameter. Ch. 2 deals with the negative-ion formation probability for hydrogen atoms. The influence of coabsorption of hydrogen is studied in Ch. 3. These measurements are important for understanding the formation process in plasma sources, because the converter surface is expected to be strongly contaminated with hydrogen. The charge state of scattered cesium particles is investigated in Ch. 4. Knowledge of this parameter is essential for Ch. 5, in which a model study of adsorption of cesium on a metal surface in contact with a plasma is presented. Finally, the negative-ion formation process in a plasma environment is studied in Ch. 6. Measurements done on a hollow-cathode discharge equipped with a novel type of converter, a porous tungsten button, are discussed. Liquid cesium diffuses through this button towards the side in contact with the plasma. (Auth.)

  13. Low jitter metal vapor vacuum arc ion source for electron beam ion trap injections

    International Nuclear Information System (INIS)

    Holland, Glenn E.; Boyer, Craig N.; Seely, John F.; Tan, J.N.; Pomeroy, J.M.; Gillaspy, J.D.

    2005-01-01

    We describe a metal vapor vacuum arc (MeVVA) ion source containing eight different cathodes that are individually selectable via the control electronics which does not require moving components in vacuum. Inside the vacuum assembly, the arc plasma is produced by means of a 30 μs pulse (26 kV,125 A) delivering 2.4 mC of charge to the cathode sample material. The trigger jitter is minimized ( 9 ions/cm 2 , measured by an unbiased Faraday cup positioned 20 cm from the extractor grid, at discharge rates up to 5 Hz. The electronic triggering of the discharge is via a fiber optic interface. We present the design, fabrication details, and performance of this MeVVA, recently installed on the National Institute of Standards and Technology electron beam ion trap (EBIT)

  14. Sensitive metal ions (II) determination with resonance Raman method

    Science.gov (United States)

    Yu, Zhi; Bracero, Lucas A.; Chen, Lei; Song, Wei; Wang, Xu; Zhao, Bing

    2013-03-01

    In this paper, a new proposal for the quantitative evaluation of divalent metal ions (M2+) is developed by the use of the competitive resonance Raman (RR)-based method. Upon excitation with light of the appropriate wavelength (532 nm), a strong electric field is generated that couples with the resonance of the complex (zincon-M2+), increasing the character signals of these complexes, resulting in sensitive detection. Herein, the RR probe, zincon-M2+ complex that the RR intensity gets lower with the decreasing of the M2+ concentration, which leads to the transformation of the Raman information. As a result, by using the proposed RR-based method, we could find the liner calibration curves of Cu2+ and Ni2+, which show the potential in quantitative evaluation of an unknown sample. In addition, the abundant fingerprint information shows that RR leads to the successful analysis of a blended solution, which contains two ions: Cu2+ and Ni2+.

  15. Vitrification and Crystallization of Phase-Separated Metallic Liquid

    Directory of Open Access Journals (Sweden)

    Yun Cheng

    2017-02-01

    Full Text Available The liquid–liquid phase separation (LLPS behavior of Fe50Cu50 melt from 3500 K to 300 K with different rapid quenching is investigated by molecular dynamics (MD simulation based on the embedded atom method (EAM. The liquid undergoes metastable phase separation by spinodal decomposition in the undercooled regime and subsequently solidifies into three different Fe-rich microstructures: the interconnected-type structure is kept in the glass and crystal at a higher cooling rate, while the Fe-rich droplets are found to crystalize at a lower cooling rate. During the crystallization process, only Fe-rich clusters can act as the solid nuclei. The twinning planes can be observed in the crystal and only the homogeneous atomic stacking shows mirror symmetry along the twinning boundary. Our present work provides atomic-scale understanding of LLPS melt during the cooling process.

  16. Measuring free metal ion concentrations in situ in natural waters using the Donnan Membrane Technique

    NARCIS (Netherlands)

    Kalis, E.J.J.; Weng, L.P.; Dousma, F.; Temminghoff, E.J.M.; Riemsdijk, van W.H.

    2006-01-01

    Metal toxicity is not related to the total but rather to the free or labile metal ion concentration. One of the techniques that can be used to measure several free metal ion concentrations simultaneously is the Donnan Membrane Technique (DMT) in combination with the inductively coupled plasma-mass

  17. PHENOL OXIDATION USING NATURAL ZEOLITE SUPPORTED METAL ION CATALYST

    Directory of Open Access Journals (Sweden)

    Sri Wardhani

    2010-06-01

    Full Text Available Phenol which contained in waste water has to be reduced and it could be done by oxygen oxidation.  In order to increase the rate of reaction it was needed a catalyst. In this research the capability of various catalysts, namely zeolite-Zn(II, zeolite-Cu(II and zeolite-Co(IIin oxidation of phenol has been investigated. The aim of this research was to study the type of metal ion catalyst towards the percentage of oxidated phenol. The oxidation process were carried out in an aqueous phenol of 100 ppm with oxygen flow rate of 200 mL/min. in the presence of catalysts with 0.2M of initial impregnation concentration. The capabilities of catalysts were performed by calculating the activation energy and it was done at two different temperatures, i.e. 70 and 90 oC. The percentage of oxidated phenol was determinated by measuring its concentration using UV-VIS spectrophotometer. In addition, the impregnated metal was calculated by measuring the ion concentration remains in the filtrate solution and it was determined using Atomic Absorption Spectrophotometer. The results showed that metal ion types affected the catalytic activity. The order of phenol oxidationactivity decreased as Co(II > Cu(II > Zn(II. The surface characteristics of catalysts were supported by pore volume and pore diameter i.e 0.009 cm3/g and 16.59 Å for Zn(II whereas specific surface area was 10.32 m2/g for Zn(II, 0.004 cm3/g and 24.37 Å for Cu(II whereas specific surface area was 3.57 m2/g for Cu(II, 0.001 cm3/g and 19.63 Å for Co(II whereas specific surface area was 10.26m2/g for Co(II.   Keywords: phenol,natural zeolite, catalyst, oxidation

  18. Mechanical behavior and failure mechanisms of Li-ion battery separators

    Science.gov (United States)

    Kalnaus, Sergiy; Wang, Yanli; Turner, John A.

    2017-04-01

    Anisotropic mechanical properties were experimentally determined and compared for three types of commercially available Li-ion battery separators: Celgard 2325, Celgard PP2075 dry-processed polymer separators, and DreamWeaver Gold 40 non-woven separator. Significant amount of anisotropy of properties was determined, with the Young's modulus being different by up to a factor of 5 and ultimate strength being different by a factor of 10 between orthogonal directions within a polymer separator layer. Strain rate sensitivity was investigated by applying strain rates ranging from 1 ṡ10-4 s-1 to 0.1 s-1. Significant strengthening was observed and the strain rate strengthening coefficients were determined for both elastic modulus and yield stress in case of polymer separators. Digital image correlation technique was used to measure and map the strains over the specimen's gage section. Significant strain concentration in bands running perpendicular to the tensile axis was observed in polymer separator samples oriented in transverse direction. Such localized necking allows for extremely high strains close to 300% to develop in the material. The failure mode was remarkably different for all three types of separators which adds additional variable in safe design of Li-ion batteries for prevention of internal short circuits.

  19. Separation of rare earths from transition metals by liquid-liquid extraction from a molten salt hydrate to an ionic liquid phase.

    Science.gov (United States)

    Rout, Alok; Binnemans, Koen

    2014-02-28

    The solvent extraction of trivalent rare-earth ions and their separation from divalent transition metal ions using molten salt hydrates as the feed phase and an undiluted fluorine-free ionic liquid as the extracting phase were investigated in detail. The extractant was tricaprylmethylammonium nitrate, [A336][NO3], and the hydrated melt was calcium nitrate tetrahydrate, Ca(NO3)2·4H2O. The extraction behavior of rare-earth ions was studied for solutions of individual elements, as well as for mixtures of rare earths in the hydrated melt. The influence of different extraction parameters was investigated: the initial metal loading in the feed phase, percentage of water in the feed solution, equilibration time, and the type of hydrated melt. The extraction of rare earths from Ca(NO3)2·4H2O was compared with extraction from CaCl2·4H2O by [A336][Cl] (Aliquat 336). The nitrate system was found to be the better one. The extraction and separation of rare earths from the transition metals nickel, cobalt and zinc were also investigated. Remarkably high separation factors of rare-earth ions over transition metal ions were observed for extraction from Ca(NO3)2·4H2O by the [A336][NO3] extracting phase. Furthermore, rare-earth ions could be separated efficiently from transition metal ions, even in melts with very high concentrations of transition metal ions. Rare-earth oxides could be directly dissolved in the Ca(NO3)2·4H2O phase in the presence of small amounts of Al(NO3)3·9H2O or concentrated nitric acid. The efficiency of extraction after dissolving the rare-earth oxides in the hydrated nitrate melt was identical to extraction from solutions with rare-earth nitrates dissolved in the molten phase. The stripping of the rare-earth ions from the loaded ionic liquid phase and the reuse of the recycled ionic liquid were also investigated in detail.

  20. Metal ion-improved complexation countercurrent chromatography for enantioseparation of dihydroflavone enantiomers.

    Science.gov (United States)

    Han, Chao; Wang, Wenli; Xue, Guimin; Xu, Dingqiao; Zhu, Tianyu; Wang, Shanshan; Cai, Pei; Luo, Jianguang; Kong, Lingyi

    2018-01-12

    Cu(II) ion was selected as an additive to improve the enantioseparation efficiency of three dihydroflavone enantiomers in high-speed counter-current chromatography (HSCCC), using hydroxypropyl-β-cyclodextrin (HP-β-CyD) as the chiral selector. The influences of important parameters, including the metal ion, the concentrations of HP-β-CyD and the Cu(II) ion, and the sample size were investigated. Under optimal conditions, three dihydroflavone enantiomers, including (±)-hesperetin, (±)-naringenin, and (±)-farrerol, were successfully enantioseparated. The chiral recognition mechanism was investigated. The enantioseparation was attributed to the different thermodynamic stabilities of the binary complexes of HP-β-CyD and (±)-hesperetin, and Cu(II) ion could enhance this difference by forming ternary complexes with the binary complexes. This Cu(II) ion-improved complexation HSCCC system exhibited improved performance for chiral separation, and therefore it has great application potential in the preparative enantioseparation of other compounds with similar skeletons. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Formation of ion clusters in the phase separated structures of neutral-charged polymer blends

    Science.gov (United States)

    Kwon, Ha-Kyung; Olvera de La Cruz, Monica

    2015-03-01

    Polyelectrolyte blends, consisting of at least one charged species, are promising candidate materials for fuel cell membranes, for their mechanical stability and high selectivity for proton conduction. The phase behavior of the blends is important to understand, as this can significantly affect the performance of the device. The phase behavior is controlled by χN, the Flory-Huggins parameter multiplied by the number of mers, as well as the electrostatic interactions between the charged backbone and the counterions. It has recently been shown that local ionic correlations, incorporated via liquid state (LS) theory, enhance phase separation of the blend, even in the absence of polymer interactions. In this study, we show phase diagrams of neutral-charged polymer blends including ionic correlations via LS theory. In addition to enhanced phase separation at low χN, the blends show liquid-liquid phase separation at high electrostatic interaction strengths. Above the critical strength, the charged polymer phase separates into ion-rich and ion-poor regions, resulting in the formation of ion clusters within the charged polymer phase. This can be shown by the appearance of multiple spinodal and critical points, indicating the coexistence of several charge separated phases. This work was performed under the following financial assistance award 70NANB14H012 from U.S. Department of Commerce, National Institute of Standards and Technology as part of the Center for Hierarchical Materials Design (CHiMaD).

  2. Studies on the dryolysis reactions of metal ions

    International Nuclear Information System (INIS)

    Baes, C.F. Jr.

    1977-01-01

    Research is reported on metallic ions produced in solutions at low concentrations as mononuclear hydrolysis products. The method for studying the mononuclear species is to measure the solubility of the oxide or hydroxide solid phase that is stable under the conditions of interest. Column solubility measurements of Al(OH) 3 (Gibbsite) in NaCl solution as a function of pH, temperature, and ionic strength are being conducted in order to better establish the stability of the intermediate species Al(OH) 2 + and Al(OH) 3 (aq)

  3. Removal and recovery of metal ions from process and waste streams using polymer filtration

    International Nuclear Information System (INIS)

    Jarvinen, G.D.; Smith, B.F.; Robison, T.W.; Kraus, K.M.; Thompson, J.A.

    1999-01-01

    Polymer Filtration (PF) is an innovative, selective metal removal technology. Chelating, water-soluble polymers are used to selectively bind the desired metal ions and ultrafiltration is used to concentrate the polymer-metal complex producing a permeate with low levels of the targeted metal ion. When applied to the treatment of industrial metal-bearing aqueous process streams, the permeate water can often be reused within the process and the metal ions reclaimed. This technology is applicable to many types of industrial aqueous streams with widely varying chemistries. Application of PF to aqueous streams from nuclear materials processing and electroplating operations will be described

  4. Enhancing biological analyses with three dimensional field asymmetric ion mobility, low field drift tube ion mobility and mass spectrometry (μFAIMS/IMS-MS) separations.

    Science.gov (United States)

    Zhang, Xing; Ibrahim, Yehia M; Chen, Tsung-Chi; Kyle, Jennifer E; Norheim, Randolph V; Monroe, Matthew E; Smith, Richard D; Baker, Erin S

    2015-10-21

    Multidimensional high throughput separations are ideal for analyzing distinct ion characteristics simultaneously in one analysis. We report on the first evaluation of a platform coupling a high speed field asymmetric ion mobility spectrometry microchip (μFAIMS) with drift tube ion mobility and mass spectrometry (IMS-MS). The μFAIMS/IMS-MS platform was used to analyze biological samples and simultaneously acquire multidimensional FAIMS compensation fields, IMS drift times, and accurate ion masses for the detected features. These separations thereby increased the overall measurement separation power, resulting in greater information content and more complete characterization of the complex samples. The separation conditions were optimized for sensitivity and resolving power by the selection of gas compositions and pressures in the FAIMS and IMS separation stages. The resulting performance provided three dimensional separations, benefitting both broad complex mixture studies and targeted analyses by improving isomeric separations and allowing detection of species obscured by interfering peaks.

  5. Metal ion interaction of an oligopeptide fragment representing the regulatory metal binding site of a CueR protein

    DEFF Research Database (Denmark)

    Jancsó, Attila; Szokolai, Hajnalka; Roszahegyi, Livia

    2013-01-01

    Metalloregulatory proteins of the MerR family are transcriptional activators that sense/control the concentration of various metal ions inside bacteria.1 The Cu+ efflux regulator CueR, similarly to other MerR proteins, possesses a short multiple Cys-containing metal binding loop close to the C......-terminus. CueR has a high selectivity for Cu+, Ag+ and Au+, but exhibits no transcriptional activity for the divalent ions Hg2+ and Zn2+.2 The two Cys- residues of the metal binding loop were shown to settle M+ ions into a linear coordination environment but other factors may also play a role in the recognition...... of cognate metal ions.2 Nevertheless, it is an interesting question whether the same sequence, when removed from the protein, shows a flexibility to adopt different coordination environments and may efficiently bind metal ions having preferences for larger coordination numbers....

  6. Novel forward osmosis process to effectively remove heavy metal ions

    KAUST Repository

    Cui, Yue

    2014-10-01

    In this study, a novel forward osmosis (FO) process for the removal of heavy metal ions from wastewater was demonstrated for the first time. The proposed FO process consists of a thin-film composite (TFC) FO membrane made from interfacial polymerization on a macrovoid-free polyimide support and a novel bulky hydroacid complex Na4[Co(C6H4O7)2]·r2H2O (Na-Co-CA) as the draw solute to minimize the reverse solute flux. The removal of six heavy metal solutions, i.e., Na2Cr2O7, Na2HAsO4, Pb(NO3)2, CdCl2, CuSO4, Hg(NO3)2, were successfully demonstrated. Water fluxes around 11L/m2/h (LMH) were harvested with heavy metals rejections of more than 99.5% when employing 1M Na-Co-CA as the draw solution to process 2000ppm(1 ppm=1 mg/L) heavy metal solutions at room temperature. This FO performance outperforms most nanofiltration (NF) processes. In addition, the high rejections were maintained at 99.5% when a more concentrated draw solution (1.5M) or feed solution (5000ppm) was utilized. Furthermore, rejections greater than 99.7% were still achieved with an enhanced water flux of 16.5LMH by operating the FO process at 60°C. The impressive heavy metal rejections and satisfactory water flux under various conditions suggest great potential of the newly developed FO system for the treatment of heavy metal wastewater. © 2014 Elsevier B.V.

  7. Separation of heavy metal from water samples--The study of the synthesis of complex compounds of heavy metal with dithiocarbamates.

    Science.gov (United States)

    Kane, Sonila; Lazo, Pranvera; Ylli, Fatos; Stafilov, Trajce; Qarri, Flora; Marku, Elda

    2016-01-01

    The toxicity and persistence of heavy metal (HM) ions may cause several problems to marine organisms and human beings. For this reason, it is growing the interest in the chemistry of sulphur donor ligands such as dithiocarbamates (DDTC), due to their applications particularly in analytical chemistry sciences. The aim of this work has been the study of heavy metal complexes with DDTC and their application in separation techniques for the preconcentration and/or removing of heavy metals from the water solutions or the water ecosystems prior to their analysis. The HM-DDTC complexes were prepared and characterized by elemental analysis, FTIR and UV-Vis spectroscopic methods. The elemental analysis and the yield of the synthesis (97.5-99.9%) revealed a good purity of the complexes. High values of complex formation yields of HM-DDTC complexes is an important parameter for quantitatively removing/and or preconcentration of heavy metal ions from water solution even at low concentration of heavy metals. Significant differences founded between the characteristic parameters of UV/Vis (λmax and ϵmax) and FTIR absorption spectra of the parent DDTC and HM-DDTC complexes revealed the complex formation. The presence of the peaks at the visible spectral zone is important to M(nd(10-m))-L electron charge transfer of the new complexes. The (C=N) (1450-1500 cm(-1)) and the un-splitting (C-S) band (950-1002 cm(-1)) in HM-DDTC FTIR spectra are important to the identification of their bidentate mode (HM[S2CNC4H10]2). The total CHCl3 extraction of trace level heavy metals from water samples after their complex formation with DDTC is reported in this article.

  8. Methodologies for evaluation of metal-organic frameworks in separation applications

    NARCIS (Netherlands)

    Krishna, R.

    2015-01-01

    Metal-organic frameworks (MOFs) offer considerable potential for separating a wide variety of mixtures. For any given separation, there are several MOFs that could be employed. Therefore, there is a need for reliable procedures for screening and ranking MOFs with regard to their anticipated

  9. Exploiting large-pore metal-organic frameworks for separations through entropic molecular mechanisms

    NARCIS (Netherlands)

    Torres-Knoop, A.; Dubbeldam, D.

    2015-01-01

    We review the molecular mechanisms behind adsorption and the separations of mixtures in metal-organic frameworks and zeolites. Separation mechanisms can be based on differences in the affinity of the adsorbate with the framework and on entropic effects. To develop next-generation adsorbents, the

  10. Electrochemical transient techniques for determination of uranium and rare-earth metal separation coefficients in molten salts

    Energy Technology Data Exchange (ETDEWEB)

    Kuznetsov, S.A. [Institute of Chemistry, Kola Science Centre, RAS, Apatity, Murmansk Region 184200, Russia (Russian Federation)]. E-mail: kuznet@chemy.kolasc.net.ru; Hayashi, H. [Japan Atomic Energy Research Institute, Tokai-mura, Naka-gun, Ibaraki-ken 319-1195 (Japan); Minato, K. [Japan Atomic Energy Research Institute, Tokai-mura, Naka-gun, Ibaraki-ken 319-1195 (Japan); Gaune-Escard, M. [Ecole Polytechnique, IUSTI-CNRS UMR 6595, University of Provence, F-13453 Marseille, Cedex 13 (France)

    2006-02-25

    The main step in the pyrometallurgical recycling process of spent nuclear fuel is a molten salt electrorefining. The knowledge of separation coefficients of actinides (U, Np, Pu and Am) and rare-earth metals (Y, La, Ce, Nd and Gd) is very important for this step. Usually the separation coefficients are evaluated from the formal standard potentials of metals in melts containing their own ions, i.e. values obtained by potentiometric method. Electrochemical experiments were carried out at 723-823 K in order to estimate separation coefficients in LiCl-KCl eutectic melt containing uranium and lanthanum trichlorides. The electrochemical behaviour of UCl{sub 3} in LiCl-KCl melt was studied by different electrochemical methods. The diffusion coefficients of U(III) were determined by linear sweep voltammetry, chronopotentiometry and chronoamperometry. The standard rate constants of charge transfer for electroreduction of uranium, U(III) + 3e{sup -} {sup {yields}} U, were calculated by the impedance spectroscopy method. The values of constants testify that electroreduction of U(III) to U is mainly controlled by the rate of charge transfer. La(III) discharge on uranium electrode was also investigated. It was shown that for the calculation of uranium and lanthanum separation coefficients it is necessary to determine the voltammetric peak potentials of U(III) and La(III), their concentration in the melt and the kinetic parameters relating to U(III) discharge such as transfer and diffusion coefficients, and standard rate constants of charge transfer.

  11. Acetabular bone density and metal ions after metal-on-metal versus metal-on-polyethylene total hip arthroplasty; short-term results

    NARCIS (Netherlands)

    Zijlstra, Wierd P.; van der Veen, Hugo C.; van den Akker-Scheek, Inge; Zee, Mark J. M.; Bulstra, Sjoerd K.; van Raay, Jos J. A. M.

    Information on periprosthetic acetabular bone density is lacking for metal-on-metal total hip arthroplasties. These bearings use cobalt-chromium instead of titanium acetabular components, which could lead to stress shielding and hence periprosthetic bone loss. Cobalt and chromium ions have

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

    International Nuclear Information System (INIS)

    Marsh, B. A.

    2014-01-01

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

  13. Metal ion detection with oligo(ethylene glycol) monolayer-modified gold nanoparticles.

    Science.gov (United States)

    Li, Guangzhao; Yang, Bin; Lu, Zhiqiang; Xia, Sijing; Feng, Hui; Zhu, Xiaoqing; Wang, Anning; Zhu, Jin

    2011-11-01

    Two colorimetric sensors of gold nanoparticles (AuNPs) modified with different oligo(ethylene glycol)-containing organic molecules have been developed to detect metal ions by ultraviolet-visible (UV-vis) extinction spectroscopy. These sensors display different responses to some metal ions. One exhibits high selectivity for Hg2+ over a variety of competitive metal ions and the other one can respond to a multitude of metal ions. These differences might result from the different functionalized end groups of the modified molecules. Coordination effect, pH response, and ionic strength were investigated to understand the mechanism of the responses to metal ions. The results suggested that the colorimetric responses were mainly induced by the coordination effect of the modified organic molecules and the removing of the modified organic molecules caused by metal ions.

  14. Most spin-1/2 transition-metal ions do have single ion anisotropy

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Jia; Whangbo, Myung-Hwan, E-mail: hxiang@fudan.edu.cn, E-mail: mike-whangbo@ncsu.edu [Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695 (United States); Koo, Hyun-Joo [Department of Chemistry and Research Institute for Basic Sciences, Kyung Hee University, Seoul 130-701 (Korea, Republic of); Xiang, Hongjun, E-mail: hxiang@fudan.edu.cn, E-mail: mike-whangbo@ncsu.edu [Key Laboratory of Computational Physical Sciences (Ministry of Education), State Key Laboratory of Surface Physics, and Department of Physics, Fudan University, Shanghai 200433 (China); Kremer, Reinhard K. [Max-Planck-Institut für Festkörperforschung, Heisenbergstrasse 1, D-70569 Stuttgart (Germany)

    2014-09-28

    The cause for the preferred spin orientation in magnetic systems containing spin-1/2 transition-metal ions was explored by studying the origin of the easy-plane anisotropy of the spin-1/2 Cu{sup 2+} ions in CuCl{sub 2}·2H{sub 2}O, LiCuVO{sub 4}, CuCl{sub 2}, and CuBr{sub 2} on the basis of density functional theory and magnetic dipole-dipole energy calculations as well as a perturbation theory treatment of the spin-orbit coupling. We find that the spin orientation observed for these spin-1/2 ions is not caused by their anisotropic spin exchange interactions, nor by their magnetic dipole-dipole interactions, but by the spin-orbit coupling associated with their crystal-field split d-states. Our study also predicts in-plane anisotropy for the Cu{sup 2+} ions of Bi{sub 2}CuO{sub 4} and Li{sub 2}CuO{sub 2}. The results of our investigations dispel the mistaken belief that magnetic systems with spin-1/2 ions have no magnetic anisotropy induced by spin-orbit coupling.

  15. On Thermocapillary Mechanism of Spatial Separation of Metal Melts

    Science.gov (United States)

    Demin, V. A.; Mizev, A. I.; Petukhov, M. I.

    2018-02-01

    Theoretical research has been devoted to the study of binary metal melts behavior in a thin capillary. Earlier it has been found experimentally that unusually significant and quick redistribution of melts components takes place along capillary after the cooling. Numerical simulation of concentration-induced convection has been carried out to explain these experimental data. Two-component melt of both liquid metals filling vertical thin capillary with non-uniform temperature distribution on the boundaries is considered. It is assumed that the condition of absolute non-wetting is valid on the sidewalls. Because of this effect there is a free surface on vertical boundaries, where thermocapillary force is appeared due to the external longitudinal temperature gradient. It makes to move liquid elements at a big distance, compared with axial size of capillary. Effects of adsorption-desorption on the surface, thermal and concentration-capillary forces, convective motion in a volume and diffusion generate the large-scale circulation. This process includes the admixture carrying-out on the surface in the more hot higher part of the channel, its following transfer down along the boundary due to the thermocapillary force and its return in the volume over the desorption in the lower part of capillary. Intensity of motion and processes of adsorption-desorption on the free boundary have the decisive influence upon the formation of concentration fields and speed of components redistribution. Thus, one of the possible mechanisms of longitudinal division on components of liquid binary mixtures in thin channels has been demonstrated.

  16. Bubble separation at the interface between a liquid metal and a liquid slag

    Science.gov (United States)

    Chevrier, Vincent F.

    Due to more specific consumer demand, most steel manufacturers are developing techniques to produce quality steels by limiting the number of defects in the final product. There are several aspects to be considered when producing "clean steels", and this research project will focus on one of them: inclusion and bubble separation. Large inclusions (solid or liquid) and gas bubbles have to be removed from the liquid metal before casting, and separation occurs mostly at the slag-metal interface. The objective of this study to develop a fundamental understanding of bubble separation at the slag-metal interface by looking at the chemical engineering literature on separation and coalescence, and by studying experimentally bubble separation at a liquid-liquid interface, first using a water-oil system and then with a metal-slag system. The literature review and the water modeling experiments have shown that four separate steps need to be considered when studying the removal of a buoyant phase particle at a liquid-liquid interface: the transport to the interface, the separation at the interface (film drainage), the film rupture and the removal from the interface. The major factors influencing the rest-time of an argon bubble at an oil-water interface are determined experimentally. The high temperature apparatus permits direct visualization of bubble behavior in metal and slag. The separation of argon bubbles at the slag-metal interface exhibits a behavior similar to what is observed in water modeling: the bubbles impact the interface and rest there for some time before coalescing. A methodology of studying the separation of solid and liquid inclusions is also established using two complementary techniques: x-ray fluoroscopy and confocal scanning electron microscopy. This experimental study showed that inclusions and bubbles do not separate immediately upon reaching the slag-metal interface but can rest in the metal phase for long periods of time before separating. Enhancing

  17. Ultrafast optical phase modulation with metallic nanoparticles in ion-implanted bilayer silica

    Energy Technology Data Exchange (ETDEWEB)

    Torres-Torres, C [Seccion de Estudios de Posgrado e Investigacion, ESIME-Z, Instituto Politecnico Nacional, Mexico, DF, 07738 (Mexico); Tamayo-Rivera, L; Silva-Pereyra, H G; Reyes-Esqueda, J A; Rodriguez-Fernandez, L; Crespo-Sosa, A; Cheang-Wong, J C; Oliver, A [Instituto de Fisica, Universidad Nacional Autonoma de Mexico, 04510, Mexico, DF (Mexico); Rangel-Rojo, R [Departamento de Optica, Centro de Investigacion Cientifica y de Educacion Superior de Ensenada Apartado Postal 360, Ensenada, BC, 22860 (Mexico); Torres-Martinez, R, E-mail: crstorres@yahoo.com.mx [Centro de Investigacion en Ciencia Aplicada y TecnologIa Avanzada Unidad Queretaro, Instituto Politecnico Nacional, Santiago de Queretaro, Queretaro, 76090 (Mexico)

    2011-09-02

    The nonlinear optical response of metallic-nanoparticle-containing composites was studied with picosecond and femtosecond pulses. Two different types of nanocomposites were prepared by an ion-implantation process, one containing Au nanoparticles (NPs) and the other Ag NPs. In order to measure the optical nonlinearities, we used a picosecond self-diffraction experiment and the femtosecond time-resolved optical Kerr gate technique. In both cases, electronic polarization and saturated absorption were identified as the physical mechanisms responsible for the picosecond third-order nonlinear response for a near-resonant 532 nm excitation. In contrast, a purely electronic nonlinearity was detected at 830 nm with non-resonant 80 fs pulses. Regarding the nonlinear optical refractive behavior, the Au nanocomposite presented a self-defocusing effect, while the Ag one presented the opposite, that is, a self-focusing response. But, when evaluating the simultaneous contributions when the samples are tested as a multilayer sample (silica-Au NPs-silica-Ag NPs-silica), we were able to obtain optical phase modulation of ultra-short laser pulses, as a result of a significant optical Kerr effect present in these nanocomposites. This allowed us to implement an ultrafast all-optical phase modulator device by using a combination of two different metallic ion-implanted silica samples. This control of the optical phase is a consequence of the separate excitation of the nonlinear refracting phenomena exhibited by the separate Au and Ag nanocomposites.

  18. Ultrafast optical phase modulation with metallic nanoparticles in ion-implanted bilayer silica

    International Nuclear Information System (INIS)

    Torres-Torres, C; Tamayo-Rivera, L; Silva-Pereyra, H G; Reyes-Esqueda, J A; Rodriguez-Fernandez, L; Crespo-Sosa, A; Cheang-Wong, J C; Oliver, A; Rangel-Rojo, R; Torres-Martinez, R

    2011-01-01

    The nonlinear optical response of metallic-nanoparticle-containing composites was studied with picosecond and femtosecond pulses. Two different types of nanocomposites were prepared by an ion-implantation process, one containing Au nanoparticles (NPs) and the other Ag NPs. In order to measure the optical nonlinearities, we used a picosecond self-diffraction experiment and the femtosecond time-resolved optical Kerr gate technique. In both cases, electronic polarization and saturated absorption were identified as the physical mechanisms responsible for the picosecond third-order nonlinear response for a near-resonant 532 nm excitation. In contrast, a purely electronic nonlinearity was detected at 830 nm with non-resonant 80 fs pulses. Regarding the nonlinear optical refractive behavior, the Au nanocomposite presented a self-defocusing effect, while the Ag one presented the opposite, that is, a self-focusing response. But, when evaluating the simultaneous contributions when the samples are tested as a multilayer sample (silica-Au NPs-silica-Ag NPs-silica), we were able to obtain optical phase modulation of ultra-short laser pulses, as a result of a significant optical Kerr effect present in these nanocomposites. This allowed us to implement an ultrafast all-optical phase modulator device by using a combination of two different metallic ion-implanted silica samples. This control of the optical phase is a consequence of the separate excitation of the nonlinear refracting phenomena exhibited by the separate Au and Ag nanocomposites.

  19. Effects of heavy metal ions on EDTA-sensitive cell contacts of Dictyostelium discoideum

    OpenAIRE

    Yoshida, Motonobu

    2000-01-01

    [Synopsis] The effects of heavy metal ions on the EDTA-sensitive cell contacts, which exist from growthphase stage of Dictyostelium discoideum, was investigated. EDTA-sensitive cell contacts of cells at the growth-phase stage were analyzed in the presence of heavy metal ions. Heavy metal ions Hg^, Cd^ and Cu^ inhibited EDTA-sensitive cell contacts at concentrations higher than 10^M, whereas Pb^ did not show any recognizable effects at the same concentration range. The possible mechanisms of a...

  20. Separation of Fluoride Ions in an Electrolytic Cell by Using an AnionExchange Membrane

    International Nuclear Information System (INIS)

    Fathurrachman; Sunardi

    2000-01-01

    Separation of fluoride ions in an electrolytic cell with an anionexchange membrane which is so-called an electrodialysis process has beenperformed. The experiment have been taken place in room temperature in anelectrolytic cell made by plexiglas consisted on anode and cathode chambersseparated by an anion exchange membrane in dimension of 4 x 4 cm. The carbonand stainless steel are applied as an anode and platinum as s' cathode. Theanolyte is a HNO 3 0.3 M solution, while a solution of NaF 0.3 M, and amixture of NaF 0.3 M containing uranyl nitrate solution for separating offluoride ions and uranium are used as a catholyte. The distance between theelectrode and the membrane is 1.5 cm and this distance is kept constant. Theparameters observed are the current voltage, cathode applied, and uraniumconcentration. For the solution without uranium, the results show that thefluoride ions transferred are around 50 % using carbon as a cathode for 3hours and the voltage of 10 volts, while for SS as a cathode are around 93 %.For the solution containing uranium, the fluoride ions transferred are around78 % for 3.5 hours and the uranium ions remain in the catholyte in which mostof them are as 8 yellow deposit of Na 2 U 2 O 7 on the cathode surface andothers are as a white precipitate of NaUF 5 on the bottom of the cathodechamber. (author)

  1. Electrospray droplet exposure to organic vapors: metal ion removal from proteins and protein complexes.

    Science.gov (United States)

    DeMuth, J Corinne; McLuckey, Scott A

    2015-01-20

    The exposure of aqueous nanoelectrospray droplets to various organic vapors can dramatically reduce sodium adduction on protein ions in positive ion mass spectra. Volatile alcohols, such as methanol, ethanol, and isopropanol lead to a significant reduction in sodium ion adduction but are not as effective as acetonitrile, acetone, and ethyl acetate. Organic vapor exposure in the negative ion mode, on the other hand, has essentially no effect on alkali ion adduction. Evidence is presented to suggest that the mechanism by which organic vapor exposure reduces alkali ion adduction in the positive mode involves the depletion of alkali metal ions via ion evaporation of metal ions solvated with organic molecules. The early generation of metal/organic cluster ions during the droplet desolvation process results in fewer metal ions available to condense on the protein ions formed via the charged residue mechanism. These effects are demonstrated with holomyoglobin ions to illustrate that the metal ion reduction takes place without detectable protein denaturation, which might be revealed by heme loss or an increase in charge state distribution. No evidence is observed for denaturation with exposure to any of the organic vapors evaluated in this work.

  2. Measurement of Cadmium Ion in the Presence of Metal-Binding Biopolymers in Aqueous Sample

    Directory of Open Access Journals (Sweden)

    Jian Pu

    2013-01-01

    Full Text Available In aqueous environment, water-soluble polymers are effectively used to separate free metal ions from metal-polymer complexes. The feasibilities of four different analytical techniques, cadmium ion-selective electrode, dialysis sack, chelate disk cartridge, and ultrafiltration, in distinguishing biopolymer-bound and nonbound cadmium in aqueous samples were investigated. And two different biopolymers were used, including bovine serum albumin (BSA and biopolymer solution extracted from cultivated activated sludge (ASBP. The ISE method requires relatively large amount of sample and contaminates sample during the pretreatment. After the long reaction time of dialysis, the equilibrium of cadmium in the dialysis sack would be shifted. Due to the sample nature, chelate disk cartridge could not filter within recommended time, which makes it unavailable for biopolymer use. Ultrafiltration method would not experience the difficulties mentioned above. Ultrafiltration method measuring both weakly and strongly bound cadmium was included in nominally biopolymer-cadmium complex. It had significant correlation with the Ion-selective electrode (ISE method (R2=0.989 for BSA, 0.985 for ASBP.

  3. Magnetic Zr-MOFs nanocomposites for rapid removal of heavy metal ions and dyes from water.

    Science.gov (United States)

    Huang, Lijin; He, Man; Chen, Beibei; Hu, Bin

    2018-05-01

    Amino-decorated Zr-based magnetic Metal-Organic Frameworks composites (Zr-MFCs) were prepared by a facile and efficient strategy. The nano-sized Fe 3 O 4 @SiO 2 core (about 15 nm) was coated with a shell of Zr-MOFs (about 5 nm) by means of in-situ growth. And, Fe 3 O 4 @SiO 2 @UiO-66 and its amino derivatives (Fe 3 O 4 @SiO 2 @UiO-66-NH 2 and Fe 3 O 4 @SiO 2 @UiO-66-Urea) were successfully prepared by using different precursors. The obtained Zr-MFCs were demonstrated to be efficient adsorbents for metal ions/organic dyes removal from aqueous solution, with high adsorption capacity and fast adsorption kinetics. It was found that the amine-decorated MFCs were highly efficient for metal ions/dyes removal compared to raw MFC-O. Among them, MFC-N exhibited the highest capacity for Pb 2+ (102 mg g -1 ) and methylene blue (128 mg g -1 ), while MFC-O exhibited the highest capacity for methyl orange (219 mg g -1 ). Moreover, anionic and cationic dyes could be selectively separated and removed from the mixed solution just by adjusting the solution pH with Zr-MFCs as the adsorbents. And these Zr-MFCs materials can be easily regenerated by desorbing metal ions/organic dyes from the sorbents with appropriate eluents, and the adsorption capacity can be remained unchanged after 6 recycles. The obtained results demonstrated the great application potential of the prepared MFCs as fascinating adsorbents for water treatment. Copyright © 2018 Elsevier Ltd. All rights reserved.

  4. Metal ion sorption by untreated and chemically treated biomass

    Energy Technology Data Exchange (ETDEWEB)

    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.

  5. Physicochemical basis of the ion-exchange separation of gold cyanide complexes

    Science.gov (United States)

    Kononova, O. N.; Kononov, Yu. S.

    2014-10-01

    The mechanism of the separation of gold cyanide complexes is discussed, along with ion exchanger selection, selectivity, elution, and industrial applications. The ion-exchange mechanism for the sorption of gold cyanide complexes is established, and a criterion is suggested for selecting the anion exchanger for their extraction (specifically, the p K a of the anion exchanger). The selectivity of the sorption of gold cyanide complexes by anion exchangers with rarely distributed ionogenic groups is demonstrated. A procedure for the elution of gold cyanide complexes using alkaline solutions is developed.

  6. Separation of halogens from uranium compounds by means of pyrohydrolysis and their determination by ion chromatography

    International Nuclear Information System (INIS)

    Pires, M.A.F.; Brandao Filho, D.; Abrao, A.

    1987-07-01

    This paper describs the determination of fluorine in nuclear grade uranium compounds by means of phyrohydrolysis. A stream of wet oxygem at a temperature of 900 to 1000 0 C is passed through a quartz tube where the powdered samples is put. The halogens are volatilized as their respective acids that are absorbed in a buffer solution or water. The measurements are made with ion-seletive eletrodes or by ion chromatography. The sensitivity is of 1μg F - /g and 5μg Cl - /g. The separation of fluorine from uranium compounds by diferent methods is discussed. (Author) [pt

  7. Evaluation of cationite efficiency during extraction of heavy metal ions from diluted solutions

    OpenAIRE

    Gomelya, Nikolai; Ivanova, Veronika; Galimova, Valentina; Nosachova, Julia; Shabliy, Tatiana

    2017-01-01

    Ion exchange is one of the methods that has been successfully employed in industry for extracting heavy metals from wastewater. We conducted research into ion-exchange processes of extraction of heavy metal ions on the weak- and strong-acid cationites from distilled and tap water. Heavy metal ion concentration was less than 1 mg/dm3. We established that in all cases efficiency of water treatment decreased at a decrease in the starting concentration of a metal. The process took place regardles...

  8. Application of monocarboxylic acids for the extraction of metal ions-literature survey

    International Nuclear Information System (INIS)

    Brzozka, Z.; Rozycki, C.

    1980-01-01

    In the paper there is presented a literature review concerning the application of monocarboxylic acids for extraction of metal ions. The following problems are discussed: characteristic of monocarboxylic acids and their mixtures, the equilibria between the acid solution in organic solvent and aqueous phase, the mechanism of acid partition, complexes of carboxylic acids and metal ions in aqueous phase, mechanism of extraction by means of carboxylic acids as well as the problems concerning the extraction of individual metal ions. Data about the extraction of metal ions are presented in table. The 138 references are given. (author)

  9. Use of divalent metal ions in the DNA cleavage reaction of topoisomerase IV

    Science.gov (United States)

    Pitts, Steven L.; Liou, Grace F.; Mitchenall, Lesley A.; Burgin, Alex B.; Maxwell, Anthony; Neuman, Keir C.; Osheroff, Neil

    2011-01-01

    It has long been known that type II topoisomerases require divalent metal ions in order to cleave DNA. Kinetic, mutagenesis and structural studies indicate that the eukaryotic enzymes utilize a novel variant of the canonical two-metal-ion mechanism to promote DNA scission. However, the role of metal ions in the cleavage reaction mediated by bacterial type II enzymes has been controversial. Therefore, to resolve this critical issue, this study characterized the DNA cleavage reaction of Escherichia coli topoisomerase IV. We utilized a series of divalent metal ions with varying thiophilicities in conjunction with oligonucleotides that replaced bridging and non-bridging oxygen atoms at (and near) the scissile bond with sulfur atoms. DNA scission was enhanced when thiophilic metal ions were used with substrates that contained bridging sulfur atoms. In addition, the metal-ion dependence of DNA cleavage was sigmoidal in nature, and rates and levels of DNA cleavage increased when metal ion mixtures were used in reactions. Based on these findings, we propose that topoisomerase IV cleaves DNA using a two-metal-ion mechanism in which one of the metal ions makes a critical interaction with the 3′-bridging atom of the scissile phosphate and facilitates DNA scission by the bacterial type II enzyme. PMID:21300644

  10. Nanoparticles reduce nickel allergy by capturing metal ions

    Science.gov (United States)

    Vemula, Praveen Kumar; Anderson, R. Rox; Karp, Jeffrey M.

    2011-05-01

    Approximately 10% of the population in the USA suffer from nickel allergy, and many are unable to wear jewellery or handle coins and other objects that contain nickel. Many agents have been developed to reduce the penetration of nickel through skin, but few formulations are safe and effective. Here, we show that applying a thin layer of glycerine emollient containing nanoparticles of either calcium carbonate or calcium phosphate on an isolated piece of pig skin (in vitro) and on the skin of mice (in vivo) prevents the penetration of nickel ions into the skin. The nanoparticles capture nickel ions by cation exchange, and remain on the surface of the skin, allowing them to be removed by simple washing with water. Approximately 11-fold fewer nanoparticles by mass are required to achieve the same efficacy as the chelating agent ethylenediamine tetraacetic acid. Using nanoparticles with diameters smaller than 500 nm in topical creams may be an effective way to limit the exposure to metal ions that can cause skin irritation.

  11. Effect of large pore size of multifunctional mesoporous microsphere on removal of heavy metal ions.

    Science.gov (United States)

    Yuan, Qing; Li, Nan; Chi, Yue; Geng, Wangchang; Yan, Wenfu; Zhao, Ying; Li, Xiaotian; Dong, Bin

    2013-06-15

    Pore size of mesoporous materials is crucial for their surface grafting. This article develops a novel multifunctional microsphere with a large pore size mesoporous silica shell (ca. 10.3 nm) and a magnetic core (Fe₃O₄), which is fabricated using cetyltrimethylammonium bromide (CTAB) as pore-forming agents, tetraethyl orthosilicate (TEOS) as silicon source through a sol-gel process. Compared with small pore size mesoporous silica magnetic microspheres (ca. 2-4 nm), the large pore size one can graft 447 mg/g amino groups in order to adsorb more heavy metal ions (Pb(2+): 880.6 mg/g, Cu(2+): 628.3mg/g, Cd(2+): 492.4 mg/g). The metal-loaded multifunctional microspheres could be easily removed from aqueous solution by magnetic separation and regenerated easily by acid treatment. The results suggest that the large pore size multifunctional microspheres are potentially useful materials for high effectively adsorbing and removing different heavy metal ions in aqueous solution. Copyright © 2013 Elsevier B.V. All rights reserved.

  12. Determination of trace transition metals in environmental matrices by chelation ion chromatography.

    Science.gov (United States)

    Murgia, Sandro M; Selvaggi, Roberta; Poletti, Antonio

    2011-03-01

    Trace transition metals (Fe(3+), Mn, Cu, Cd, Co, Zn, Ni) in environmental samples were analyzed by chelation ion chromatography using a mixed bed ion-exchange column with pyridine-2,6-dicarboxylic acid (PDCA) and oxalic acid as eluent and large volume direct injection (1,000 μl). The two eluents, PDCA and oxalic acid, were tested, and repeatability and detection limits were compared. The total analysis time was ~15 min. The separation with PDCA was more successful than that obtained with acid oxalic. It was observed that utilizing PDCA resulted in lower detection limits, higher repeatability, and a quantitative detection of Cd and Mn, which coelute as a single peak when using the oxalic acid. At last, the PDCA calibration graphs resulted linear (r (2) > 0.999) in the range 0.4-1,000 μg/L. The procedure was applied to the analysis of metals in soils and in water samples. The results obtained from the analysis of natural waters have demonstrated that the method is simple and efficient, therefore, can be used for the determination of metals in natural waters using a continuous and automatic monitoring system.

  13. Application of the hybrid complexation-ultrafiltration process for metal ion removal from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Zeng Jianxian [College of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201 (China) and College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)], E-mail: zengjianxian@163.com; Ye Hongqi [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Hu Zhongyu [College of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201 (China)

    2009-01-30

    Complexation-ultrafiltration process was investigated for mercury and cadmium removal from aqueous solutions by using poly(acrylic acid) sodium salt (PAASS) as a complexing agent. The kinetics of complexation reactions of PAASS with the metal ions were studied under a large excess PAASS and pH 5.5. It takes 25 and 50 min for mercury and cadmium to get the complexation equilibrium, respectively, and the reaction kinetics can be described by a pseudo-first-order equation. Effects of various operating parameters such as loading ratios, pH values, etc. on metal rejection coefficients (R) were investigated. In the process of concentration, membrane fluxes decline slowly and R values are about 1. The concentrated retentates were used further for the decomplexation. The decomplexation ratio of mercury-PAASS complex is about 30%, whereas that of cadmium-PAASS complex reaches 93.5%. After the decomplexation, diafiltration experiments were carried out at pH 2.5. Cadmium can be diafiltrated satisfactorily from the retentate, but for mercury it is the contrary. Selective separation of the both metal ions was studied from a binary solution at pH 5. When mercury, cadmium and PAASS concentrations are 30, 30 and 40 mg L{sup -1}, respectively, mercury is retained by ultrafiltration while almost all cadmium passes through the membrane.

  14. Accelerated electron exchange between U4+ and UO22+ by foreign metal ions

    International Nuclear Information System (INIS)

    Obanawa, Heiichiro; Onitsuka, Hatsuki; Takeda, Kunihiko

    1990-01-01

    The rate constant of U 4+ -UO 2 2+ electron exchange (k et ) was increased by more than 100 times in the presence of various metal ions. The larger rate constant was observed for the smaller difference of the standard reduction potential strength between metal ion and UO 2 2+ ion (Δμ θ e ). Detailed investigation of the electron exchange reaction in the presence of Mo 5+ suggested that the mechanism of the electron transfer reaction catalyzed by metal ions is the outer-sphere type independent of U-Clcomplex ions. (author)

  15. Prostate cancer outcome and tissue levels of metal ions

    Science.gov (United States)

    Sarafanov, A.G.; Todorov, T.I.; Centeno, J.A.; MacIas, V.; Gao, W.; Liang, W.-M.; Beam, C.; Gray, Marion A.; Kajdacsy-Balla, A.

    2011-01-01

    BACKGROUNDThere are several studies examining prostate cancer and exposure to cadmium, iron, selenium, and zinc. Less data are available on the possible influence of these metal ions on prostate cancer outcome. This study measured levels of these ions in prostatectomy samples in order to examine possible associations between metal concentrations and disease outcome.METHODSWe obtained formalin fixed paraffin embedded tissue blocks of prostatectomy samples of 40 patients with PSA recurrence, matched 1:1 (for year of surgery, race, age, Gleason grading, and pathology TNM classification) with tissue blocks from 40 patients without recurrence (n = 80). Case–control pairs were compared for the levels of metals in areas adjacent to tumors. Inductively coupled plasma-mass spectrometry (ICP-MS) was used for quantification of Cd, Fe, Zn, and Se.RESULTSPatients with biochemical (PSA) recurrence of disease had 12% lower median iron (95 µg/g vs. 111 µg/g; P = 0.04) and 21% lower zinc (279 µg/g vs. 346 µg/g; P = 0.04) concentrations in the normal-appearing tissue immediately adjacent to cancer areas. Differences in cadmium (0.489 µg/g vs. 0.439 µg/g; 4% higher) and selenium (1.68 µg/g vs. 1.58 µg/g; 5% higher) levels were not statistically significant in recurrence cases, when compared to non-recurrences (P = 0.40 and 0.21, respectively).CONCLUSIONSThere is an association between low zinc and low iron prostate tissue levels and biochemical recurrence in prostate cancer. Whether these novel findings are a cause or effect of more aggressive tumors, or whether low zinc and iron prostatic levels raise implications for therapy, remains to be investigated. 

  16. Metal carbonates as anode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    Shao, Lianyi; Ma, Rui; Wu, Kaiqiang; Shui, Miao; Lao, Mengmeng; Wang, Dongjie; Long, Nengbing; Ren, Yuanlong; Shu, Jie

    2013-01-01

    Highlights: •Metal carbonates are probable anode materials for lithium ion batteries. •CoCO 3 /C composite can deliver an initial discharge capacity of 2096.6 mAh g −1 . •Co, Li 2 CO 3 , Li 2 O, and low-valence carbon are final lithiated products for CoCO 3 . -- Abstract: Six metal carbonates (Li 2 CO 3 , Na 2 CO 3 , SrCO 3 , BaCO 3 , K 2 CO 3 , CoCO 3 ) are tested and compared as anode materials for lithium ion batteries. The electrochemical results show that only CoCO 3 is electrochemically active material and can deliver a high initial capacity of 1425.9 mAh g −1 . The lithium storage mechanism in CoCO 3 is studied by ex situ X-ray diffraction technique, ex situ infrared method, ex situ X-ray photoelectron spectroscopy and in situ X-ray diffraction technique. It is found that the electrochemical reactions between CoCO 3 and Li firstly result in the formation of metal Co and Li 2 CO 3 , and then partial Li 2 CO 3 is further reduced into carbon (C 0 ), low-valence carbon (C 2+ ), and Li 2 O. It also demonstrates that the electrochemical reaction between CoCO 3 and Li is a partially reversible process. Based on these electrochemical results, it is obvious that narrow potential range can acquire a better reversibility for CoCO 3 /Li batteries by suppressing particle pulverization. Besides, the comparison of CoCO 3 , ball-milled CoCO 3 and ball-milled CoCO 3 /C composite also indicates that smaller active particle and carbon buffer are beneficial to obtain better cycling performance and higher reversible capacity

  17. Electrospun polyimide nanofiber-based nonwoven separators for lithium-ion batteries

    Science.gov (United States)

    Miao, Yue-E.; Zhu, Guan-Nan; Hou, Haoqing; Xia, Yong-Yao; Liu, Tianxi

    2013-03-01

    Polyimide (PI) nanofiber-based nonwovens have been fabricated via electrospinning for the separators of lithium-ion batteries (LIBs). Differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and hot oven tests show that the PI nanofiber-based nonwovens are thermally stable at a high temperature of 500 °C while the commercial Celgard membrane exhibits great shrinkage at 150 °C and even goes melting over 167 °C, indicating a superior thermal stability of PI nanofiber-based nonwovens than that of the Celgard membrane. Moreover, the PI nanofiber-based nonwovens exhibit better wettability for the polar electrolyte compared to the Celgard membrane. The PI nanofiber-based nonwoven separators are also evaluated to have higher capacity, lower resistance and higher rate capability compared to the Celgard membrane separator, which proves that they are ideal candidates for separators of high-performance rechargeable LIBs.

  18. Novel modified poly vinyl chloride blend membranes for removal of heavy metals from mixed ion feed sample

    Energy Technology Data Exchange (ETDEWEB)

    Nayak, Vignesh; Jyothi, M.S. [Centre for Nano and Material Sciences, Jain University, Jain Global Campus, Kanakapura Ramanagaram, Bangalore, 562112 (India); Balakrishna, R. Geetha, E-mail: br.geetha@jainuniversity.ac.in [Centre for Nano and Material Sciences, Jain University, Jain Global Campus, Kanakapura Ramanagaram, Bangalore, 562112 (India); Padaki, Mahesh, E-mail: sp.mahesh@jainuniversity.ac.in [Centre for Nano and Material Sciences, Jain University, Jain Global Campus, Kanakapura Ramanagaram, Bangalore, 562112 (India); National University of Science and Technology “MISIS”, Moscow, 119049 (Russian Federation); Deon, Sebastien [Institut UTINAM, UMR CNRS 6213, Université de Bourgogne-Franche-Comté,16 route de Gray, Besançon Cedex 25030 (France)

    2017-06-05

    Highlights: • Work reports the novel modification of poly vinyl chloride (PVC) using newly developed method. • Blend membranes were prepared using modified PVC and polysulfone in different compositions. • The prepared blend membranes were used for separation of different heavy metal ions. • The blend membranes showed improved rejection of heavy metal ions in comparison to Commercial NF 270 membrane. - Abstract: Herein, an attempt has been made to prepare a novel membrane with good efficiency for removal of heavy metal ions namely lead (Pb), cadmium (Cd) and chromium (Cr). 4-amino benzoic acid (ABA) was covalently grafted onto the poly vinyl chloride (PVC) backbone by C−N bond to enhance the hydrophilicity. {sup 1}H NMR and ATR-IR spectroscopy analysis confirmed the chemical modification of PVC. Further the modified polymer was blended in different compositions with polysulfone (PSf) for optimization. Morphological changes that occurred in blend membranes, due to the incorporation of modified PVC was studied by AFM and SEM techniques. The effect on hydrophilicity and performance of blends owing to incorporation of modified PVC was evaluated by water uptake, contact angle and flux studies. The density of functional groups in blends was analyzed by its ion-exchange capacity. Batch wise filtration of metal ions was carried out and the effect of pressure, feed pH and interference of ions was thoroughly investigated. Essentially, 100% rejection was obtained for all the metal ions in acidic pH with a productivity of 2.56 l/m{sup 2} h. The results were correlated with the results of commercially available NF 270 membrane under the same operating conditions.

  19. Novel modified poly vinyl chloride blend membranes for removal of heavy metals from mixed ion feed sample

    International Nuclear Information System (INIS)

    Nayak, Vignesh; Jyothi, M.S.; Balakrishna, R. Geetha; Padaki, Mahesh; Deon, Sebastien

    2017-01-01

    Highlights: • Work reports the novel modification of poly vinyl chloride (PVC) using newly developed method. • Blend membranes were prepared using modified PVC and polysulfone in different compositions. • The prepared blend membranes were used for separation of different heavy metal ions. • The blend membranes showed improved rejection of heavy metal ions in comparison to Commercial NF 270 membrane. - Abstract: Herein, an attempt has been made to prepare a novel membrane with good efficiency for removal of heavy metal ions namely lead (Pb), cadmium (Cd) and chromium (Cr). 4-amino benzoic acid (ABA) was covalently grafted onto the poly vinyl chloride (PVC) backbone by C−N bond to enhance the hydrophilicity. 1 H NMR and ATR-IR spectroscopy analysis confirmed the chemical modification of PVC. Further the modified polymer was blended in different compositions with polysulfone (PSf) for optimization. Morphological changes that occurred in blend membranes, due to the incorporation of modified PVC was studied by AFM and SEM techniques. The effect on hydrophilicity and performance of blends owing to incorporation of modified PVC was evaluated by water uptake, contact angle and flux studies. The density of functional groups in blends was analyzed by its ion-exchange capacity. Batch wise filtration of metal ions was carried out and the effect of pressure, feed pH and interference of ions was thoroughly investigated. Essentially, 100% rejection was obtained for all the metal ions in acidic pH with a productivity of 2.56 l/m 2 h. The results were correlated with the results of commercially available NF 270 membrane under the same operating conditions.

  20. Heavy metal ion removal by adsorption on to biological materials

    International Nuclear Information System (INIS)

    Jansson-Charrier, M.; Guibal, E.; Le Cloirec, P.; Surjous, R.

    1994-01-01

    The development of regulations constraints in the industrial waste-waters management leads to the study of new treatment processes, using raw or functionalized biological materials. These processes show competitive performances in metal ion sorption efficiency for the low metal content effluents. Uptake capacities of Uranium as high as 400 mg.g -1 chitosan, equivalent to the double of the uptake capacity of fungal origin biomass, can be reached. The application of these processes to real mine wastewaters gives efficiency coefficient upper to 90%, the residual concentrations are compatible to a direct injection into the environment. The grafting of functional groups onto the chitosan scales up the sorption performances to uptake capacity upper than 600 mg.g -1 polymer. pH, metal concentration are cited as major parameters, particle size influences both uptake kinetics and sorption equilibrium, in the case of the uranium accumulation by chitosan. The desorption of uranium from the sorbent allows the valorization of uranium and the re-use of the sorbent. (authors). 21 refs., 10 figs

  1. Towards metals analysis using corona discharge ionization ion mobility spectrometry.

    Science.gov (United States)

    Jafari, Mohammad T; Saraji, Mohammad; Sherafatmand, Hossein

    2016-02-25

    For the first time, the capability of corona discharge ionization ion mobility spectrometry (CD-IMS) in the determination of metal complex was evaluated. The extreme simplicity of dispersive liquid-liquid microextraction (DLLME) coupled to the high sensitivity of CD-IMS measurement could make this combination really useful for simple, rapid, and sensitive determination of metals in different samples. In this regard, mercury, as a model metal, was complexed with diethyldithiocarbamate (DEDTC), and then extracted into the carbon tetrachloride using DLLME. Some parameters affecting the extraction efficiency, including the type and volume of the extraction solvent, the type and volume of the disperser solvent, the concentration of the chelating agent, salt addition and, pH were exhaustively investigated. Under the optimized condition, the enrichment factor was obtained to be 142. The linear range of 0.035-10.0 μg mL(-1) with r(2) = 0.997 and the detection limit of 0.010 μg mL(-1) were obtained. The relative standard deviation values were calculated to be lower than 4% and 8% for intra-day and inter-day, respectively. Finally, the developed method was successfully applied for the extraction and determination of mercury in various real samples. The satisfactory results revealed the capability of the proposed method in trace analysis without tedious derivatization or hydride generation. Copyright © 2016 Elsevier B.V. All rights reserved.

  2. Observation of water separated ion-pairs between cations and phospholipid headgroups.

    Science.gov (United States)

    van der Post, Sietse T; Hunger, Johannes; Bonn, Mischa; Bakker, Huib J

    2014-04-24

    In this work, we present evidence for ion pair formation of cations with a high surface charge density (Na(+) and Ca(2+)) and phosphate groups of phospholipids. We used femto-second infrared pump-probe and dielectric spectroscopy to probe the dynamics of water molecules in solutions of phosphorylethanolamine and different types of cations. We find that sodium and calcium cooperatively retard the dynamics of water in solutions of phosphorylethanolamine, implying the formation of solvent separated ion pairs. This ion-specific interaction is absent for potassium, cesium and ammonium. We compare our results to dielectric spectroscopy experiments, which probes the rotation of all dipolar molecules and ions in solution. The rotation of the dipolar phosphorylethanolamine ion shows that long-lived ion-pairs are only formed with calcium and not with ammonium, cesium, potassium, and sodium. This finding implies that the association between calcium and the phosphate is strong with lifetimes exceeding 200 ps, while the interaction with sodium is relatively short-lived (∼20-100 ps).

  3. Outcome of revision arthroplasty for failed metal-on-metal total hip replacements; is there a relation with metal ions?

    Science.gov (United States)

    Iqbal, Hafiz J; Al-Azzani, Waheeb A K; Jackson-Taylor, Esther; Clatworthy, Elizabeth; John, Alun

    2017-05-12

    We aimed to assess the early outcome following revision arthroplasty for failed metal-on-metal (MoM) total hip replacements (THR) due to adverse reaction to metal debris (ARMD). We reviewed 106 consecutive revision arthroplasties. Case notes and radiological investigations were reviewed to assess the complications. Oxford Hip Score (OHS) and Euroqol (EQ-5D-3L) scores were used to assess the functional outcome and improvement of quality of life. At a mean follow-up of 20 months (12-48 months), the mean OHS was 28.7. Pain improved in 61% patients. A majority of patients were in level 2 for all the EQ-5D-3L dimensions. The overall complication rate was 16%. Survivorship free from further revision for any cause was 94.3% at 48 months. There was no correlation between pre-revision blood metal ions and the final outcome. Revision surgery for failed MoM hip replacement due to ARMD is associated with a relatively higher rate of complications and risk of chronic pain. There is poor correlation between serum metal ions and development of ARMD and outcome following revision surgery.

  4. Surface modification by metal ion implantation forming metallic nanoparticles in an insulating matrix

    International Nuclear Information System (INIS)

    Salvadori, M.C.; Teixeira, F.S.; Sgubin, L.G.; Cattani, M.; Brown, I.G.

    2014-01-01

    Highlights: • Metal nanoparticles can be produced through metallic ion implantation in insulating substrate, where the implanted metal self-assembles into nanoparticles. • The nanoparticles nucleate near the maximum of the implantation depth profile, that can be estimated by computer simulation using the TRIDYN. • Nanocomposites, obtained by this way, can be produced in different insulator materials. More specifically we have studied Au/PMMA (polymethylmethacrylate), Pt/PMMA, Ti/alumina and Au/alumina systems. • The nanocomposites were characterized by measuring the resistivity of the composite layer as function of the dose implanted, reaching the percolation threshold. • Excellent agreement was found between the experimental results and the predictions of the theory. - Abstract: There is special interest in the incorporation of metallic nanoparticles in a surrounding dielectric matrix for obtaining composites with desirable characteristics such as for surface plasmon resonance, which can be used in photonics and sensing, and controlled surface electrical conductivity. We have investigated nanocomposites produced by metal ion implantation into insulating substrates, where the implanted metal self-assembles into nanoparticles. The nanoparticles nucleate near the maximum of the implantation depth profile (projected range), which can be estimated by computer simulation using the TRIDYN code. TRIDYN is a Monte Carlo simulation program based on the TRIM (Transport and Range of Ions in Matter) code that takes into account compositional changes in the substrate due to two factors: previously implanted dopant atoms, and sputtering of the substrate surface. Our study show that the nanoparticles form a bidimentional array buried a few nanometers below the substrate surface. We have studied Au/PMMA (polymethylmethacrylate), Pt/PMMA, Ti/alumina and Au/alumina systems. Transmission electron microscopy of the implanted samples show that metallic nanoparticles form in

  5. Thiophilic metal ion rescue of phosphorothioate interference within the Tetrahymena ribozyme P4-P6 domain.

    OpenAIRE

    Basu, S; Strobel, S A

    1999-01-01

    Divalent metal ions are essential for the folding and catalytic activities of many RNAs. A commonly employed biochemical technique to identify metal-binding sites in RNA is the rescue of Rp alpha-phosphorothioate (PS) interference by the addition of soft divalent metal ions. To access the ability of such experiments to accurately identify metal-ion coordinations within a complex RNA fold, we report metal-rescue results from the Tetrahymena group I intron P4-P6 domain, where the location and c...

  6. Functional separator consisted of polyimide nonwoven fabrics and polyethylene coating layer for lithium-ion batteries

    Science.gov (United States)

    Shi, Chuan; Zhang, Peng; Huang, Shaohua; He, Xinyi; Yang, Pingting; Wu, Dezhi; Sun, Daoheng; Zhao, Jinbao

    2015-12-01

    In this paper, a composite membrane with nonwoven polyimide (PI) membrane as structural support and polyethylene (PE) particles coating layer as a thermal shutdown layer, is fabricated as the separator for lithium-ion battery. Different from PI nonwoven membrane, the PE coating PI nonwoven composite membrane (PE-PI-S) not only shows excellent thermal shutdown function, similar to traditional multilayer PP/PE/PP separator, but also exhibits much higher thermal stability, better wettability to the polar electrolyte and lower internal resistance than the PP/PE/PP separator. The electrolyte uptake and ionic conductivity of PE-PI-S increase from 58%, 0.84 mS cm-1 to 400%, 1.34 mS cm-1, respectively. Furthermore, the thermal shutdown function of PE-PI-S can be controlled widely in the temperature range from 120 °C to more than 200 °C while the multilayer PP/PE/PP separator only with a shutdown temperature range from 130 °C to 160 °C. Lithium ion battery with PE-PI-S nonwoven separator also shows excellent stable cycling and good rate performance.

  7. Electrospun montmorillonite modified poly(vinylidene fluoride) nanocomposite separators for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Fang, Changjiang; Yang, Shuli; Zhao, Xinfei [College of Materials and Textile, Zhejiang Sci-Tech University, Hangzhou 310018 (China); Du, Pingfan, E-mail: dupf@zstu.edu.cn [College of Materials and Textile, Zhejiang Sci-Tech University, Hangzhou 310018 (China); Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Ministry of Education), Zhejiang Sci-Tech University, Hangzhou 310018 (China); Xiong, Jie, E-mail: jxiong@zstu.edu.cn [College of Materials and Textile, Zhejiang Sci-Tech University, Hangzhou 310018 (China); Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Ministry of Education), Zhejiang Sci-Tech University, Hangzhou 310018 (China)

    2016-07-15

    Highlights: • Composite separators of PVDF and MMT for lithium-ion batteries were electrospun. • Thermal dimensional stability and tensile property of composite separators get improved. • Presence of montmorillonite promotes electrical properties of PVDF fibrous separators. • Batteries consisting of PVDF/MMT-5% separator achieve the best performance. - Abstract: Composite separators of poly(vinylidene fluoride) (PVDF) with different contents of montmorillonite (MMT) for Li-ion batteries have been fabricated by electrospinning. The morphology, function group, crystallinity, and mechanical properties of membranes were investigated by scanning electron microscope (SEM), Fourier Transform infrared spectra (FT-IR), differential scanning calorimetry (DSC), and tensile test, respectively. Interlayer spacing of MMT in polymer was characterized by X-ray diffraction (XRD). In addition, the results of electrochemical measurements suggest that PVDF/MMT-5% composite membrane has maximum ionic conductivity of 4.2 mS cm{sup −1}, minimum interfacial resistance of 97 Ω, and excellent electrochemical stability. The cell comprising PVDF/MMT-5% composite membrane shows higher capacity and more stable cycle performance than the one using commercial Celgard PP membrane.

  8. Swift heavy ion induced modification in polycarbonate membrane for gas separation

    International Nuclear Information System (INIS)

    Rajesh Kumar; Prasad, Rajendra; Vijay, Y.K.; Das, D.

    2003-01-01

    Polymeric membranes are extensively used for commercial gas separation applications. Makrofol-KG (polycarbonate) is a glassy polymer. 40 μm thick sheet of Makrofol-KG was irradiated with 40 Ar (14.9 MeV/n) of fluence 10 3 ions/cm 2 and 20 μm thick sheet with 5.3 MeV α-particles of fluence 10 7 ions/cm 2 . The permeability of these polycarbonate membranes for H 2 and CO 2 was measured and also after etching in 6 N NaOH at 60 degC for different periods. Permeability is found to be increased with etching time. At a definite time, critical etching time, the permeability rapidly increases in PC. Positron annihilation lifetimes for unirradiated and irradiated membranes were measured with fast fast coincidence system to study the correlation of free volume hole concentration with gas separation properties. (author)

  9. A study of an ion-exchange process for separation of strontium and yttrium

    International Nuclear Information System (INIS)

    Mubarek, M.A.

    1980-01-01

    A study has been carried out to determine optimum conditions for the separation of strontium and yttrium by ion-exchange. The parameters of interest for such separation such as the dimensions of the ion-exchange columns, flow rates through the columns and pH values of the solutions, which affect the overall yield in the process, have been investigated. Application of this method for routine quantitative determinations of Sr-90 in environmental samples, particularly the wet-ashed biological materials has also been studied. The method, although a rapid and convenient one has not been found to yield consistent results probably due to the requirement of stringent analytical controls during the process. (author)

  10. Water-soluble polymers for recovery of metal ions from aqueous streams

    Science.gov (United States)

    Smith, Barbara F.; Robison, Thomas W.

    1998-01-01

    A process of selectively separating a target metal contained in an aqueous solution by contacting the aqueous solution containing a target metal with an aqueous solution including a water-soluble polymer capable of binding with the target metal for sufficient time whereby a water-soluble polymer-target metal complex is formed, and, separating the solution including the water-soluble polymer-target metal complex from the solution is disclosed.

  11. Some aspects of metallic ion chemistry and dynamics in the mesosphere and thermosphere

    Science.gov (United States)

    Mathews, J. D.

    1987-01-01

    The relationship between the formation of sporadic layers of metallic ion and the dumping of these ions into the upper mesosphere is discussed in terms of the tidal wind, classical (i.e., windshear) and other more complex, perhaps highly nonlinear layer formation mechanisms, and a possible circulation mechanism for these ions. Optical, incoherent scatter radar, rocket, and satellite derived evidence for various layer formation mechanisms and for the metallic ion circulation system is reviewed. The results of simple one dimensional numerical model calculations of sporadic E and intermediate layer formation are presented along with suggestions for more advanced models of intense or blanketing sporadic E. The flux of metallic ions dumped by the tidal wind system into the mesosphere is estimated and compared with estimates of total particle flux of meteoric origin. Possible effects of the metallic ion flux and of meteoric dust on D region ion chemistry are discussed.

  12. Ion-implantation-induced phase separation and crystallization in lithia-silica glasses

    International Nuclear Information System (INIS)

    Arnold, G.W.; Peercy, P.S.; Doyle, B.L.

    1980-01-01

    Crystallization of annealed Li 2 O.2SiO 2 glasses implanted with inert ions and fused SiO 2 glass implanted with Li ions was monitored using infrared reflection spectroscopy. Elastic recoil detection analysis was used to study changes in the Li and H concentration induced in these glasses by implantation and annealing. Implantation of Li 2 O.2SiO 2 with inert ions results in Li depletion, accompanied by H indiffusion, in the implanted region. For Li-implanted SiO 2 , crystallization of α-quartz is accompanied by appreciable Li diffusion to the surface and attendant H migration to the Li-depleted region. The crystallization mechanisms are discussed in terms of phase separation in the lithia-silica system

  13. Ion chromatographic separation for analysis of radiostrontium in nuclear reprocessing solutions of high ionic strength

    International Nuclear Information System (INIS)

    Lamb, J.D.; Nordmeyer, F.R.; Drake, P.A.; Elder, M.P.; Miles, R.W.

    1989-01-01

    An ion chromatography (IC)-based method was developed for Sr 2+ concentration and separation showing high recoveries of strontium. This procedure permits complete automation. One of the potential weaknesses of the IC approach to sample preconcentration, i.e. sensitivity to solutions of high acid content, common in nuclear reprocessing solution, has been overcome by a novel application of acid suppression technology. (author) 12 refs.; 8 figs.; 3 tabs

  14. Strain distribution and failure mode of polymer separators for Li-ion batteries under biaxial loading

    Science.gov (United States)

    Kalnaus, Sergiy; Kumar, Abhishek; Wang, Yanli; Li, Jianlin; Simunovic, Srdjan; Turner, John A.; Gorney, Phillip

    2018-02-01

    Deformation of polymer separators for Li-ion batteries has been studied under biaxial tension by using a dome test setup. This deformation mode provides characterization of separator strength under more complex loading conditions, closer representing deformation of an electric vehicle battery during crash event, compared to uniaxial tension or compression. Two polymer separators, Celgard 2325 and Celgard 2075 were investigated by deformation with spheres of three different diameters. Strains in separators were measured in situ by using Digital Image Correlation (DIC) technique. The results show consistent rupture of separators along the machine direction coinciding with areas of high strain accumulation. The critical first principal strain for failure was independent of the sphere diameter and was determined to be approximately 34% and 43% for Celgard 2325 and Celgard 2075 respectively. These values can be taken as a criterion for internal short circuit in a battery following an out-of-plane impact. A Finite Element (FE) model was built with the anisotropic description of separator behavior, derived from tensile tests in orthogonal directions. The results of simulations predicted the response of separator rather well when compared to experimental results for various sizes of rigid sphere.

  15. Separation of ions in nanofluidic channels with combined pressure-driven and electro-osmotic flow.

    Science.gov (United States)

    Gillespie, Dirk; Pennathur, Sumita

    2013-03-05

    Separation of ionic species with the same electrophoretic mobility but different valence in electrolyte systems can occur within nanometer-scale channels with finite electrical double layers (EDLs). This is because EDL thicknesses are a significant fraction of slit height in such channels and can create transverse analyte concentration profiles that allow for unique separation modalities when combined with axial fluid flow. Previous work has shown such separation to occur using either pressure-driven flow or electro-osmotic flow separately. Here, we develop a Poisson-Boltzmann model to compare the separation of such ions using the combination of both pressure-driven and electro-osmotic flow. Applying a pressure gradient in the opposite direction of electro-osmotic flow can allow for zero or infinite retention of analyte species, which we investigate using three different wall boundary conditions. Furthermore, we determine conditions in fused silica nanochannels with which to generate optimal separation between two analytes of different charge but the same mobility. We also give simple rules of thumb to achieve the best separation efficacy in nanochannel systems.

  16. Application of reverse osmosis membrane for separation of toxic metal in water

    International Nuclear Information System (INIS)

    Syahril Ahmad

    2010-01-01

    Experimental separation of toxic metal in water has been done using reverse osmosis membrane made from composite material. Experiment was done by simulation in which metals that will be observed solved with water in different concentration and then used as feed solution in reverse osmosis process. Metals observed were Cr 6+ , Mn 2+ and Pb 2+ and reverse osmosis process was done at pressure of 40 Bar for all metals. Experiment result showed that value of feed solution concentration would affect flux and coefficient rejection of membrane. Composite membrane with polyacrylamide as active layer of membrane can reject metals observed with value of rejection coefficient more than 90%, except for Mn 2+ metal that have concentration 250 ppm and 500 ppm. (author)

  17. Thermosensitive gels incorporating polythioether units for the selective extraction of class b metal ions.

    Science.gov (United States)

    Chayama, K; Morita, Y; Iwatsuki, S

    2010-10-22

    Novel temperature-responsive copolymers of N-isopropylacrylamide and monoaza-tetrathioether derivative, were synthesized for the selective extraction of soft metal ions such as silver(I), copper(I), gold(III) and palladium(II) ion. The ratio between N-isopropylacrylamide group and monoaza-tetrathioether group in the copolymer was determined. The ratio between N-isopropylacrylamide group and monoaza-tetrathioether group varied in the range of 66:1-187:1. Each lower critical solution temperature (LCST) of the polymer solution was determined spectrophotometrically by the relative absorbance change at 750 nm via temperature of the polymer solution. Metal ion extraction using the copolymer with appropriate counter anions such as picrate ion, nitrate or perchlorate ion was examined. Soft metal ions such as silver(I), copper(I), gold(III) and palladium(II) ion were extracted selectively into the solid polymer phase. The extraction efficiency of a metal ion such as silver ion increased as the increase of the ratio of the monoaza-tetrathioether group to N-isopropylacrylamide group in the polymer. The quantitative extraction of class b metal ions as well as the liquid-liquid extraction of metal ions with monoaza-tetrathioether molecule was performed. Copyright © 2010 Elsevier B.V. All rights reserved.

  18. First laser ions at an off-line mass separator of the ISAC facility at TRIUMF

    CERN Document Server

    Rauth, C; Horn, R; Lassen, J; Bricault, P; Wendt, K; 10.1016/j.nimb.2003.08.029

    2004-01-01

    For efficient and in particular for selective production of radioactive ion beams at on-line mass separator facilities the technique of resonance ionization laser ion sources (RILlS) has become the most powerful tool. In facilities like ISOLDE at CERN they nowadays represent the most commonly used type of ion source for rare short-lived isotopes, delivering highest suppression of isobaric contaminations. For a first off-line demonstration preparing the development and installation of such a laser ion source at the new ISAC facility at TRIUMF in Vancouver (Canada), an all solid state laser system developed at the University of Mainz (Germany), was transferred and tested there at an off-line test separator. The laser system consists of three tunable titanium:sapphire lasers with a repetition rate of 12 kHz, pulse length of ~30 ns, up to 2.5 W output power in the infrared to red spectral region and features additional frequency doubling units. With this system first RILIS studies were performed in a number of el...

  19. Application of retention modelling to the simulation of separation of organic anions in suppressed ion chromatography.

    Science.gov (United States)

    Zakaria, Philip; Dicinoski, Greg W; Ng, Boon Khing; Shellie, Robert A; Hanna-Brown, Melissa; Haddad, Paul R

    2009-09-18

    The ion-exchange separation of organic anions of varying molecular mass has been demonstrated using ion chromatography with isocratic, gradient and multi-step eluent profiles on commercially available columns with UV detection. A retention model derived previously for inorganic ions and based solely on electrostatic interactions between the analytes and the stationary phase was applied. This model was found to accurately describe the observed elution of all the anions under isocratic, gradient and multi-step eluent conditions. Hydrophobic interactions, although likely to be present to varying degrees, did not limit the applicability of the ion-exchange retention model. Various instrumental configurations were investigated to overcome problems associated with the use of organic modifiers in the eluent which caused compatibility issues with the electrolytically derived, and subsequently suppressed, eluent. The preferred configuration allowed the organic modifier stream to bypass the eluent generator, followed by subsequent mixing before entering the injection valve and column. Accurate elution prediction was achieved even when using 5-step eluent profiles with errors in retention time generally being less than 1% relative standard deviation (RSD) and all being less than 5% RSD. Peak widths for linear gradient separations were also modelled and showed good agreement with experimentally determined values.

  20. Metal ions, not metal-catalyzed oxidative stress, cause clay leachate antibacterial activity.

    Directory of Open Access Journals (Sweden)

    Caitlin C Otto

    Full Text Available Aqueous leachates prepared from natural antibacterial clays, arbitrarily designated CB-L, release metal ions into suspension, have a low pH (3.4-5, generate reactive oxygen species (ROS and H2O2, and have a high oxidation-reduction potential. To isolate the role of pH in the antibacterial activity of CB clay mixtures, we exposed three different strains of Escherichia coli O157:H7 to 10% clay suspensions. The clay suspension completely killed acid-sensitive and acid-tolerant E. coli O157:H7 strains, whereas incubation in a low-pH buffer resulted in a minimal decrease in viability, demonstrating that low pH alone does not mediate antibacterial activity. The prevailing hypothesis is that metal ions participate in redox cycling and produce ROS, leading to oxidative damage to macromolecules and resulting in cellular death. However, E. coli cells showed no increase in DNA or protein oxidative lesions and a slight increase in lipid peroxidation following exposure to the antibacterial leachate. Further, supplementation with numerous ROS scavengers eliminated lipid peroxidation, but did not rescue the cells from CB-L-mediated killing. In contrast, supplementing CB-L with EDTA, a broad-spectrum metal chelator, reduced killing. Finally, CB-L was equally lethal to cells in an anoxic environment as compared to the aerobic environment. Thus, ROS were not required for lethal activity and did not contribute to toxicity of CB-L. We conclude that clay-mediated killing was not due to oxidative damage, but rather, was due to toxicity associated directly with released metal ions.

  1. MeRNA: a Database of Metal Ion Binding Sites in RNAStructures

    Energy Technology Data Exchange (ETDEWEB)

    Stefan, Liliana R.; Zhang, Rui; Levitan, Aaron G.; Hendrix, DonnaF.; Brenner, Steven E.; Holbrook, Stephen R.

    2005-10-05

    Metal ions are essential for the folding of RNA into stable tertiary structures and for the catalytic activity of some RNA enzymes. To aid in the study of the roles of metal ions in RNA structural biology, we have created MeRNA (Metals in RNA), a comprehensive compilation of all metal binding sites identified in RNA three-dimensional structures available from the Protein Data Bank (PDB) and Nucleic Acid Database (NDB). Currently, our database contains information relating to binding of 9764 metal ions corresponding to 23 distinct elements; in 256 RNA structures. The metal ion locations were confirmed and ligands characterized using original literature references. MeRNA includes eight manually identified metal-ion binding motifs, which are described in the literature. MeRNA is searchable by PDB identifier, metal ion, method of structure determination, resolution and R-values for X-ray structure, and distance from metal to any RNA atom or to water. New structures with their respective binding motifs will be added to the database as they become available. The MeRNA database will further our understanding of the roles of metal ions in RNA folding and catalysis and have applications in structural and functional analysis, RNA design and engineering.

  2. Cleavage reactions of the complex ions derived from self-complementary deoxydinucleotides and alkali-metal ions using positive ion electrospray ionization with tandem mass spectrometry.

    Science.gov (United States)

    Xiang, Yun; Abliz, Zeper; Takayama, Mitsuo

    2004-05-01

    The dissociation reactions of the adduct ions derived from the four self-complementary deoxydinucleotides, d(ApT), d(TpA), d(CpG), d(GpC), and alkali-metal ions were studied in detail by positive ion electrospray ionization multiple-stage mass spectrometry (ESI-MS(n)). For the [M + H](+) ions of the four deoxydinucleotides, elimination of 5'-terminus base or loss of both of 5'-terminus base and a deoxyribose were the major dissociation pathway. The ESI-MS(n) spectra showed that Li(+), Na(+), and Cs(+) bind to deoxydinucleotides mainly by substituting the H(+) of phosphate group, and these alkali-metal ions preferred to bind to pyrimidine bases rather than purine bases. For a given deoxydinucleotide, the dissociation pathway of [M + K](+) ions differed clearly from that of [M + Li](+), [M + Na](+), and [M + Cs](+) ions. Some interesting and characteristic cleavage reactions were observed in the product-ion spectra of [M + K](+) ions, including direct elimination of deoxyribose and HPO(3) from molecular ions. The fragmentation behavior of the [M + K](+) and [M + W](+) (W = Li, Na, Cs) adduct ions depend upon the sequence of bases, the interaction between alkali-metal ions and nucleobases, and the steric hindrance caused by bases.

  3. Superior lithium adsorption and required magnetic separation behavior of iron-doped lithium ion-sieves

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Shulei; Zheng, Shili; Wang, Zheming; Cui, Wenwen; Zhang, Hailin; Yang, Liangrong; Zhang, Yi; Li, Ping

    2018-01-01

    The recent research on adsorption-based lithium recovery from lithium-containing solutions has been centred on adsorption capacity and separation of lithium ion-sieves powder from solutions. Herein, an effective iron-doped lithium titanium oxide (Fe-doped Li2TiO3) was synthesized by Fe-doping via solid state reactions followed by acid treatment to form iron-doped lithium ion-sieves (Fe/Ti-x(H)). The resulting solid powder displays both superior adsorption capacity of lithium and high separation efficiency of the adsorbent from the solutions. SEM imaging and BET surface area measurement results showed that at Fe doping levels x0.15, Fe-doping led to grain shrinkage as compared to Li2TiO3 and at the same time the BET surface area increased. The Fe/Ti-0.15(H) exhibited saturated magnetization values of 13.76 emu g-1, allowing effective separation of the material from solid suspensions through the use of a magnet. Consecutive magnetic separation results suggested that the Fe/Ti-0.15(H) powders could be applied at large-scale and continuously removed from LiOH solutions with separation efficiency of 96% or better. Lithium adsorption studies indicated that the equilibrium adsorption capacity of Fe/Ti-0.15(H) in LiOH 2 solutions (1.8 g L-1 Li, pH 12) reached 53.3 mg g-1 within 24 h, which was higher than that of pristine Li2TiO3 (50.5 mg g-1) without Fe doping. Competitive adsorption and regeneration results indicated that the Fe/Ti-0.15(H) possessed a high selectivity for Li with facile regeneration. Therefore, it could be expected that the iron-doped lithium ion-sieves have practical applicability potential for large scale lithium extraction and recovery from lithium-bearing solutions.

  4. Recovery of ferrous and nonferrous metal from ASR by physical separation

    Science.gov (United States)

    Kim, Min-gyu; Han, Oh-hyung; Park, Chul-hyun

    2017-04-01

    A recycle ratio of waste automobiles in Korea is low, compared to that of the advanced countries. Especially in its recycle, separation of automotive shredder residue (ASR), the residual fraction of approximate 25% obtained after dismantling and shredding from waste car, is needed. However ASR is cannot be effectively separated due to its heterogeneous materials and coated or laminated complexes and then is largely deposited in land-fill sites as waste. In this study ASR was separated by a series of physical processing operations such as comminution, air classification and magnetic separation and electrostatic separations. In particular it focuses on estimating the optimal conditions of magnetic and electrostatic separations for improving the separation efficiency of valuable ferrous and non-ferrous metals such as iron (Fe), aluminum, copper and etc. In magnetic separation, 91.5% Fe grade and 91% recovery could be obtained at conditions of particle size under 10mm and magnetic intensity of 400 gauss. In corona electrostatic separation for recovering nonferrous metals, a grade of 79.2% and recovery of 90.7% could be successfully achieved under conditions of -6mm particle size, 50kV electrode potential, 35rpm drum speed and 20 degree splitter position, respectively. Acknowledgments This study was supported by the R&D Center for Valuable Recycling (Global-Top R&BD Program) of the Ministry of Environment. (Project No. 2016002250001)

  5. An improved ion-exchange separation of rare-earth elements for spectrographic analysis

    International Nuclear Information System (INIS)

    Jones, E.A.

    1978-01-01

    Rare-earth elements are separated from scandium and base metals by adsorption onto anion resin BIORAD AG1-X8 in the nitrate form from a mixture of 5 per cent 7M nitric acid and 95 per cent methanol. The yttrium subgroup is eluted with a mixture of 45 per cent 7M nitric acid and 55 per cent methanol, followed by elution of the cerium subgroup with 8M nitric acid. This separation facilitates the determination of the traces of the heavier yttrium subgroup of rare-earth elements

  6. Metal ion extractant in microemulsions: where solvent extraction and surfactant science meet

    International Nuclear Information System (INIS)

    Bauer, C.

    2011-01-01

    The presented work describes the supramolecular structure of mixtures of a hydrophilic surfactant n-octyl-beta-glucoside (C8G1), and the hydrophobic metal ion extractant tributylphosphate (TBP) in n-dodecane/water as well as in the presence of salts. In the first part, basic solvent extraction system, composed of water, oil and extractant, will be introduced. The focus, however, lies on the extraction of multivalent metal ions from the aqueous phase. During this extraction process and in the following thermodynamic equilibrium, aggregation and phase transition in supramolecular assemblies occur, which are already described in literature. Notably, these reports rest on individual studies and specific conclusions, while a general concept is still missing. We therefore suggest the use of generalized phase diagrams to present the physico-chemical behaviour of (amphiphilic) extractant systems. These phase diagrams facilitated the development of a thermodynamic model based on molecular geometry and packing of the extractant molecules in the oil phase. As a result, we are now in the position to predict size and water content of extractant aggregates and, thus, verify the experimental results by calculation.Consequently, the second part presents a systematic study of the aqueous and organic phase of water/C8G1 and water/oil/TBP mixtures. The focus lies on understanding the interaction between metal ions and both amphiphilic molecules by means of small angle x-ray scattering (SAXS), dynamic light scattering (DLS) and UV-Vis spectroscopy. We confirmed the assumption that extraction of metal ions is driven by TBP, while C8G1 remains passive. In the third and last part, microemulsions of C8G1, TBP, water (and salt) and n-dodecane are characterized by small angle neutron scattering (SANS), and chemical analytics (Karl Fischer, total organic carbon, ICP-OES,...). The co-surfactant behaviour of TBP was highlighted by comparison to the classical n-alcohol (4≤n≤8) co

  7. A new design of the sputter type metal ion source and its characteristics of ion beam extraction

    International Nuclear Information System (INIS)

    Kim, W.; Choi, B.H.; Jin, J.T.; Jung, K.S.; Do, S.H.; Chung, K.H.

    1993-01-01

    In an attempt to get a high current metal ion beam of various solid elements including refractory metals, a gaseous duoPIGatron ion source was modified by placing a grid type cathode and a sputter target in the PIG chamber. Tungsten mesh was adopted as the cathode grid, and Ar gas was used for a support gas for sputter induction. For Cu, Fe, and Al, ion current and ratio of the metal ion were obtained at various conditions of sputtering voltage, support gas pressure, arc current, magnet current, and beam extraction voltage. Results showed that the metal current density is linearly changed with the sputtering voltage and magnet current. Ratio of the metal ion in the total current is larger at lower support gas pressure. Current densities for Al, Cu, and Fe were 4 mA/cm 2 , 5.5 mA/cm 2 , and 2 mA/cm 2 , respectively, at an arc current of 3 A, extraction voltage of 20 kV, and a sputtering voltage of 1 kV. Ratios of the metals in the extracted ion currents were 9%, 8%, and 5% for Al, Cu, and Fe, respectively

  8. High energy metal ion implantation using 'Magis', a novel, broad-beam, Marx-generator-based ion source

    International Nuclear Information System (INIS)

    Anders, A.; Brown, I.G.; Dickinson, M.R.; MacGill, R.A.

    1996-08-01

    Ion energy of the beam formed by an ion source is proportional to extractor voltage and ion charge state. Increasing the voltage is difficult and costly for extraction voltage over 100 kV. Here we explore the possibility of increasing the charge states of metal ions to facilitate high-energy, broad beam ion implantation at a moderate voltage level. Strategies to enhance the ion charge state include operating in the regimes of high-current vacuum sparks and short pulses. Using a time-of-flight technique we have measured charge states as high as 7+ (73 kA vacuum spark discharge) and 4+ (14 kA short pulse arc discharge), both for copper, with the mean ion charge states about 6.0 and 2.5, respectively. Pulsed discharges can conveniently be driven by a modified Marx generator, allowing operation of ''Magis'' with a single power supply (at ground potential) for both plasma production and ion extraction

  9. Ion-irradiation studies of cascade damage in metals

    International Nuclear Information System (INIS)

    Averback, R.S.

    1982-03-01

    Ion-irradiation studies of the fundamental aspects of cascade damage in metals are reviewed. The emphasis of these studies has been the determination of the primary state of damage (i.e. the arrangement of atoms in the cascade region prior to thermal migration of defects). Progress has been made towards understanding the damage function (i.e. the number of Frenkel pairs produced as a function of primary recoil atom energy), the spatial configuration of vacancies and interstitials in the cascade and the cascade-induced mixing of atoms. It is concluded for these studies that the agitation of the lattice in the vicinity of energetic displacement cascades stimulates the defect motion and that such thermal spike motion induces recombination and clustering of Frenkel defects. 9 figures

  10. Effect of metal ion hydration on the interaction between sodium carboxylates and aluminum(III) or chromium(III) ions in aqueous solution.

    Science.gov (United States)

    Pereira, Rui F P; Tapia, Maria J; Valente, Artur J M; Burrows, Hugh D

    2012-01-10

    The interaction between sodium octanoate, decanoate, and dodecanoate and aluminum(III) and chromium(III) has been studied in water at natural pH values, starting well below the surfactant critical micelle concentration, using electrical conductivity, turbidity, and potentiometric measurements. With decanoate or dodecanoate, maximum interaction occurs at 3:1 stoichiometry, corresponding to charge neutralization. Although the solutions become turbid with both metal ions, indicating phase separation, differences are observed and attributed to the fact that aluminum(III) is relatively labile to substitution and rapidly replaces its water ligands, whereas chromium(III) is substitution inert. This shows up in well-defined floc formation with Al(3+), whereas Cr(3+) suspensions do not precipitate, probably because that replacement of coordinated water by carboxylate ligands is impeded. This can be overcome by increasing temperature, and differences in the thermal behavior with Al(3+) and Cr(3+) are suggested to be due to increased involvement of substitution reactions in the latter case. The effect of octanoate on the trivalent metal ions is less clear, and with Cr(3+) interaction only occurs when the carboxylate is in excess. Hydrophobic interactions between alkyl chains play a major role in driving phase separation. At high surfactant concentrations, the solid phases do not dissolve, in contrast to what is observed with the corresponding alkylsulfates. This has implications for use of these systems in metal separation through froth flotation. The concentration of metal ions in supernatant solution has been determined for sodium dodecanoate and sodium dodecylsulfate with Al(3+) and Cr(3+) over the whole surfactant concentration range by inductively coupled plasma-mass spectrometry (ICP-MS). From this, association constants have been determined and are found to be larger for the carboxylate than the alkylsulfate, in agreement with the greater Lewis basicity of the -CO(2

  11. Analysis of space-charge effects on the ion beam in a magnetic sector-type mass separator

    International Nuclear Information System (INIS)

    Nakai, A.

    1988-01-01

    Profiles of ion beams in a magnetic sector-type mass separator are analysed by comparing with calculated ion trajectories from viewpoint of the space-charge effect; the calculation is based on a new method which takes into account the space-charge effect analytically. In the analysis, the space-charge potential in the ion beam, an axial third order aberration at the ion beam source, the space-charge neutralization and a beam of neutral particles accompanied by the ion beam are discussed. Influences of the space-charge of the primary ions are also shown to be important in the analysis of the secondary electrons. (author)

  12. Interaction of High Flash Point Electrolytes and PE-Based Separators for Li-Ion Batteries

    Science.gov (United States)

    Hofmann, Andreas; Kaufmann, Christoph; Müller, Marcus; Hanemann, Thomas

    2015-01-01

    In this study, promising electrolytes for use in Li-ion batteries are studied in terms of interacting and wetting polyethylene (PE) and particle-coated PE separators. The electrolytes are characterized according to their physicochemical properties, where the flow characteristics and the surface tension are of particular interest for electrolyte–separator interactions. The viscosity of the electrolytes is determined to be in a range of η = 4–400 mPa∙s and surface tension is finely graduated in a range of γL = 23.3–38.1 mN∙m−1. It is verified that the technique of drop shape analysis can only be used in a limited matter to prove the interaction, uptake and penetration of electrolytes by separators. Cell testing of Li|NMC half cells reveals that those cell results cannot be inevitably deduced from physicochemical electrolyte properties as well as contact angle analysis. On the other hand, techniques are more suitable which detect liquid penetration into the interior of the separator. It is expected that the results can help fundamental researchers as well as users of novel electrolytes in current-day Li-ion battery technologies for developing and using novel material combinations. PMID:26343636

  13. Interaction of High Flash Point Electrolytes and PE-Based Separators for Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Andreas Hofmann

    2015-08-01

    Full Text Available In this study, promising electrolytes for use in Li-ion batteries are studied in terms of interacting and wetting polyethylene (PE and particle-coated PE separators. The electrolytes are characterized according to their physicochemical properties, where the flow characteristics and the surface tension are of particular interest for electrolyte–separator interactions. The viscosity of the electrolytes is determined to be in a range of η = 4–400 mPa∙s and surface tension is finely graduated in a range of γL = 23.3–38.1 mN∙m−1. It is verified that the technique of drop shape analysis can only be used in a limited matter to prove the interaction, uptake and penetration of electrolytes by separators. Cell testing of Li|NMC half cells reveals that those cell results cannot be inevitably deduced from physicochemical electrolyte properties as well as contact angle analysis. On the other hand, techniques are more suitable which detect liquid penetration into the interior of the separator. It is expected that the results can help fundamental researchers as well as users of novel electrolytes in current-day Li-ion battery technologies for developing and using novel material combinations.

  14. Separation of Aliphatic and Aromatic Carboxylic Acids by Conventional and Ultra High Performance Ion Exclusion Chromatography.

    Science.gov (United States)

    Mansour, Fotouh R; Kirkpatrick, Christine L; Danielson, Neil D

    2013-06-01

    An ion exclusion chromatography (IELC) comparison between a conventional ion exchange column and an ultra-high performance liquid chromatography (UHPLC) dynamically surfactant modified C18 column for the separation of an aliphatic carboxylic acid and two aromatic carboxylic acids is presented. Professional software is used to optimize the conventional IELC separation conditions for acetylsalicylic acid and the hydrolysis products: salicylic acid and acetic acid. Four different variables are simultaneously optimized including H 2 SO 4 concentration, pH, flow rate, and sample injection volume. Thirty different runs are suggested by the software. The resolutions and the time of each run are calculated and feed back to the software to predict the optimum conditions. Derringer's desirability functions are used to evaluate the test conditions and those with the highest desirability value are utilized to separate acetylsalicylic acid, salicylic acid, and acetic acid. These conditions include using a 0.35 m M H 2 SO 4 (pH 3.93) eluent at a flow rate of 1 mL min -1 and an injection volume of 72 μL. To decrease the run time and improve the performance, a UHPLC C18 column is used after dynamic modification with sodium dodecyl sulfate. Using pure water as a mobile phase, a shorter analysis time and better resolution are achieved. In addition, the elution order is different from the IELC method which indicates the contribution of the reversed-phase mode to the separation mechanism.

  15. An Aqueous Metal-ion Capacitor with Oxidised Carbon Nanotubes and Metallic Zinc Electrodes

    Directory of Open Access Journals (Sweden)

    Yuheng Tian

    2016-10-01

    Full Text Available An aqueous metal ion capacitor comprising of a zinc anode, an oxidized carbon nanotubes (oCNTs cathode and a zinc sulfate electrolyte is reported. Since the shuttling cation is Zn2+, this typical metal ion capacitor is named as zinc-ion capacitor (ZIC. The ZIC integrates the divalent zinc stripping/plating chemistry with the surface-enabled pseudocapacitive cation adsorption/desorption on oCNTs. The surface chemistry and crystallographic structure of oCNTs were extensively characterized by combining X-ray photoelectron spectroscopy, Fourier-transformed infrared spectroscopy, Raman spectroscopy and X-ray powder diffraction. The function of the surface oxygen groups in surface cation storage was elucidated by a series of electrochemical measurement and the surface-enabled ZIC showed better performance than the ZIC with an un-oxidized CNT cathode. The reaction mechanism at the oCNT cathode involves the additional reversible Faradaic process, while the CNTs merely show electric double layer capacitive behavior involving a non-Faradaic process. The aqueous hybrid ZIC comprising the oCNT cathode exhibited a specific capacitance of 20 mF cm-2 (corresponding to 53 F g-1 in the range of 0-1.8 V at 10 mV s-1 and a stable cycling performance up to 5000 cycles.

  16. Isomer Information from Ion Mobility Separation of High-Mannose Glycan Fragments.

    Science.gov (United States)

    Harvey, David J; Seabright, Gemma E; Vasiljevic, Snezana; Crispin, Max; Struwe, Weston B

    2018-03-05

    Extracted arrival time distributions of negative ion CID-derived fragments produced prior to traveling-wave ion mobility separation were evaluated for their ability to provide structural information on N-linked glycans. Fragmentation of high-mannose glycans released from several glycoproteins, including those from viral sources, provided over 50 fragments, many of which gave unique collisional cross-sections and provided additional information used to assign structural isomers. For example, cross-ring fragments arising from cleavage of the reducing terminal GlcNAc residue on Man 8 GlcNAc 2 isomers have unique collision cross-sections enabling isomers to be differentiated in mixtures. Specific fragment collision cross-sections enabled identification of glycans, the antennae of which terminated in the antigenic α-galactose residue, and ions defining the composition of the 6-antenna of several of the glycans were also found to have different cross-sections from isomeric ions produced in the same spectra. Potential mechanisms for the formation of the various ions are discussed and the estimated collisional cross-sections are tabulated. Graphical Abstract ᅟ.

  17. Chitosan-transition metal ions complexes for selective arsenic(V) preconcentration.

    Science.gov (United States)

    Shinde, Rakesh N; Pandey, A K; Acharya, R; Guin, R; Das, S K; Rajurkar, N S; Pujari, P K

    2013-06-15

    Chitosan is naturally occurring bio-polymer having strong affinity towards transition metal ions. Chitosan complexed with transition metal ions takes up inorganic arsenic anions from aqueous medium. In present work, As(V) sorption in the chitosan complexed with different metal ions like Cu(II), Fe(III), La(III), Mo(VI) and Zr(IV) were studied. Sorptions of As(V) in CuS embedded chitosan, (3-aminopropyl) triethoxysilane (APTS) embedded chitosan, epichlorohydrin (ECH) crosslinked chitosan and pristine chitosan were also studied. (74)As radiotracer was prepared specifically for As(V) sorption studies by irradiation of natural germanium target with 18 MeV proton beam. The sorption studies indicated that Fe(III) and La(III) complexed with chitosan sorbed 95 ± 2% As(V) from aqueous samples in the pH range of 3-9. However, Fe(III)-chitosan showed better sorption efficiency (91 ± 2%) for As(V) from seawater than La(III)-chitosan (80 ± 2%). Therefore, Fe(III)-chitosan was selected to prepare the self-supported membrane and poly(propylene) fibrous matrix supported sorbent. The experimental As(V) sorption capacities of the fibrous and self-supported Fe(III)-chitosan sorbents were found to be 51 and 109 mg g(-1), respectively. These materials were characterized by XRD, SEM and EDXRF, and used for preconcentration of As(V) in aqueous media like tap water, ground water and seawater. To quantify the As(V) preconcentrated in Fe(III)-chitosan, the samples were subjected to instrumental neutron activation analysis (INAA) using reactor neutrons. As(V) separations were carried out using a two compartments permeation cell for the self-supported membrane and flow cell using the fibrous sorbent. The total preconcentration of arsenic content was also explored by converting As(III) to As(V). Copyright © 2013 Elsevier Ltd. All rights reserved.

  18. Polyethylene terephthalate/poly(vinylidene fluoride) composite separator for Li-ion battery

    International Nuclear Information System (INIS)

    Wu, Dezhi; Huang, Shaohua; Xiao, Zhiming; Zhu, Rui; Sun, Daoheng; Lin, Liwei; Xu, Zhiqin; Shi, Chuan; Zhao, Jinbao

    2015-01-01

    Electrospun nanofiber membranes have been proved to enhance the performance of a Li-ion battery (LIB), but their poor mechanical strength hinders their industrial application. This paper combines a meltblown polyethylene terephthalate (PET) nonwoven and a electrospun poly(vinylidene fluoride) (PVDF) membrane together to improve the mechanical property via hot-pressing, wherein a dried 3 wt% PVDF solution coating on PET nonwoven is used as a binder. The experiment results indicate that the hot-pressing PET/PVDF separator exhibits an excellent mechanical property, whose transverse and longitudinal tensile strength could reach 13.70 MPa and 34.85 MPa respectively. Compared with a commercial PP separator, the hot-pressing PET/PVDF membrane separator shows better wettability, higher thermal shrinkage and excellent discharge capacity as well. (paper)

  19. Polyethylene terephthalate/poly (vinylidene fluoride) composite separator for Li-ion battery

    International Nuclear Information System (INIS)

    Wu, Dezhi; Huang, Shaohua; Xiao, Zhiming; Zhu, Rui; Sun, Daoheng; Lin, Liwei; Xu, Zhiqin; Shi, Chuan; Zhao, Jinbao

    2015-01-01

    Electrospun nanofiber membranes have been proved to enhance performances of Li-ion batteries, but their poor mechanical strength hinders their industrial application. This paper combines meltblown polyethylene terephthalate (PET) nonwoven and electrospun poly (vinylidene fluoride) (PVDF) membrane together to improve the mechanical property via hot-pressing, wherein a dried 3 wt% PVDF solution coating on PET nonwoven is used as a binder. The hot-pressing temperature is optimized to be 145 °C and the composite PET/PVDF separator exhibits an excellent mechanical property, whose transverse and longitudinal tensile strength could reach 13.70 and 34.85 MPa respectively. Compared with a commercial PP separator, the hot-pressed PET/PVDF membrane separator shows better wettability, higher thermal shrinkage and improved electrochemical performance as well. (paper)

  20. The ion-electron correlation function in liquid metals

    International Nuclear Information System (INIS)

    Takeda, S.; Tamaki, S.; Waseda, Y.

    1985-01-01

    The structure factors of liquid Zn at 723 K, Sn at 523 K and Bi at 573 K have been determined by neutron diffraction with sufficient accuracy and compared with those of X-ray diffraction. A remarkable difference in the structural information between the two methods is clearly found around the first peak region as well as in the slightly varied peak positions, and it is apparently larger than the experimental errors. With these facts in mind, a new method evaluating the ion-electron correlation function in liquid metals has been proposed by using the measured structural data of X-rays and neutrons, with the help of theoretical values of the electron-electron correlation function by he Utsumi-Ichimaru scheme. This method has been applied to liquid Zn, Sn and Bi, and the radial distribution function of valence electrons around an ion has been estimated, from which the ionic radius and the schematic diagram of the electron distribution map are obtained. The ionic radii evaluated in this work have been found to agree well with those proposed by Pauling. (author)