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Sample records for valuable metal ion

  1. Selective recovery of valuable metals from spent Li-ion batteries using solvent-impregnated resins.

    Science.gov (United States)

    Guo, Fuqiang; Nishihama, Syouhei; Yoshizuka, Kazuharu

    2013-01-01

    Selective recovery of valuable metals (Cu(2+), Co(2+) and Li(+)) from leachate of spent lithium-ion (Li-ion) batteries was investigated in acidic chloride media using solvent impregnated resins (SIRs). An SIR containing bis(2-ethylhexyl) phosphoric acid (D2EHPA) had high selectivity for Fe(3+) and Al(3+), with an order of selectivity Fe(3+) > Al(3+) > Cu(2+) > Co(2+). Fe(3+) and Al(3+) could be removed from synthetic leachate by precipitation, followed by column adsorption with the SIR containing D2EHPA. The synthetic leachate was then applied to chromatography for selective recovery of Cu(2+), Co(2+) and Li(+). The solution was first fed upward to a column packed with an SIR containing 2-ethylhexylphosphonic acid mono-2-ethylhexyl ester (PC-88A) for selective separation of Cu(2+), followed by upward feed to another column packed with an SIR comprising PC-88A and bis(2,4,4-trimethylpentyl) phosphinic acid (Cyanex 272) for selective recovery of Co(2+). Finally, a column packed with a synergistic SIR containing both 1-phenyl-1,3-tetradecanedione (C11phbetaDK) and tri-n-octylphosphine oxide (TOPO) was used for selective recovery of Li(+). A process flowsheet is proposed for selective recovery of Cu(2+), Co(2+) and Li(+) using several SIRs. This process was found to be simple and efficient for selective recovery of valuable metals from leachate of spent Li-ion batteries. Pure copper, cobalt and lithium products were obtained, with high elution yields.

  2. Recovery of valuable metals from spent lithium-ion batteries by ultrasonic-assisted leaching process

    Science.gov (United States)

    Li, Li; Zhai, Longyu; Zhang, Xiaoxiao; Lu, Jun; Chen, Renjie; Wu, Feng; Amine, Khalil

    2014-09-01

    The anticipated significant use of lithium-ion batteries (LIBs) for energy storage applications in electric grid modernization and vehicle electrification shall generate a large quantity of solid waste that could become potential environmental hazards and waste natural resources. Recycling of the major components from spent LIBs is, therefore, considered desirable to prevent environmental pollution and to recycle valuable metals. This study reports on the application of ultrasonic-assisted technology to the leaching of cobalt and lithium from the cathode active materials of spent LIBs. Three acids were tested for the leaching process: two inorganic acids (H2SO4 and HCl) and one organic acid (citric acid, C6H8O7·H2O). The results show that the leaching of Co and Li is more efficient with citric acid than with the two inorganic acids. More than 96% Co and nearly 100% Li were recovered from spent LIBs. The optimal leaching conditions were 0.5 M citric acid with 0.55 M H2O2, a solid-to-liquid ratio of 25 g L-1, a temperature of 60 °C, leaching time of 5 h, and ultrasonic power of 90 W. The high leaching efficiency is mainly ascribed to the unique cavitation action of the ultrasonic waves. This ultrasonic-assisted leaching process with organic acid is not only effective but also environmentally friendly.

  3. Bioleaching of valuable metals from spent lithium-ion mobile phone batteries using Aspergillus niger

    Science.gov (United States)

    Horeh, N. Bahaloo; Mousavi, S. M.; Shojaosadati, S. A.

    2016-07-01

    In this paper, a bio-hydrometallurgical route based on fungal activity of Aspergillus niger was evaluated for the detoxification and recovery of Cu, Li, Mn, Al, Co and Ni metals from spent lithium-ion phone mobile batteries under various conditions (one-step, two-step and spent medium bioleaching). The maximum recovery efficiency of 100% for Cu, 95% for Li, 70% for Mn, 65% for Al, 45% for Co, and 38% for Ni was obtained at a pulp density of 1% in spent medium bioleaching. The HPLC results indicated that citric acid in comparison with other detected organic acids (gluconic, oxalic and malic acid) had an important role in the effectiveness of bioleaching using A. niger. The results of FTIR, XRD and FE-SEM analysis of battery powder before and after bioleaching process confirmed that the fungal activities were quite effective. In addition, bioleaching achieved higher removal efficiency for heavy metals than the chemical leaching. This research demonstrated the great potential of bio-hydrometallurgical route to recover heavy metals from spent lithium-ion mobile phone batteries.

  4. Recovery of valuable metals from waste cathode materials of spent lithium-ion batteries using mild phosphoric acid.

    Science.gov (United States)

    Chen, Xiangping; Ma, Hongrui; Luo, Chuanbao; Zhou, Tao

    2017-03-15

    Sustainable recycling of valuable metals from spent lithium-ion batteries (LIBs) may be necessary to alleviate the depletion of strategic metal resources and potential risk of environmental pollution. Herein a hydrometallurgical process was proposed to explore the possibility for the recovery of valuable metals from the cathode materials (LiCoO2) of spent LIBs using phosphoric acid as both leaching and precipitating agent under mild leaching conditions. According to the leaching results, over 99% Co can be separated and recovered as Co3(PO4)2 in a short-cut process involved merely with leaching and filtrating, under the optimized leaching conditions of 40°C (T), 60min (t), 4 vol.% H2O2, 20mLg-1 (L/S) and 0.7mol/L H3PO4. Then leaching kinetics was investigated based on the logarithmic rate kinetics model and the obtained results indicate that the leaching of Co and Li fits well with this model and the activation energies (Ea) for Co and Li are 7.3 and 10.2kJ/mol, respectively. Finally, it can be discovered from characterization results that the obtained product is 97.1% pure cobalt phosphate (Co3(PO4)2). Copyright © 2016 Elsevier B.V. All rights reserved.

  5. Recovery of valuable metals from waste cathode materials of spent lithium-ion batteries using mild phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xiangping, E-mail: chenxiangping101@163.com [School of Environmental Science and Engineering, Shaanxi University of Science & Technology, Xi’an 710021 (China); College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Ma, Hongrui, E-mail: mahr@sust.edu.cn [School of Environmental Science and Engineering, Shaanxi University of Science & Technology, Xi’an 710021 (China); Luo, Chuanbao; Zhou, Tao [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)

    2017-03-15

    Graphical abstract: Cobalt can be directly recovered as Co{sub 3}(PO{sub 4}){sub 2} from waste LiCoO{sub 2} using H{sub 3}PO{sub 4} as leaching and precipitating agent. - Highlights: • Phosphoric acid was innovatively used as leaching and precipitating agent. • Over 99% Co and Li can be separated and recovered in a single leaching step. • Co and Li can be separated under mild conditions of 40 °C and 0.7 M H{sub 3}PO{sub 4}. • Activation energy values for Co and Li are 7.3 and 10.168 kJ/mol. • Cobalt phosphate (97.1% in purity) can be obtained as the leaching product. - Abstract: Sustainable recycling of valuable metals from spent lithium-ion batteries (LIBs) may be necessary to alleviate the depletion of strategic metal resources and potential risk of environmental pollution. Herein a hydrometallurgical process was proposed to explore the possibility for the recovery of valuable metals from the cathode materials (LiCoO{sub 2}) of spent LIBs using phosphoric acid as both leaching and precipitating agent under mild leaching conditions. According to the leaching results, over 99% Co can be separated and recovered as Co{sub 3}(PO{sub 4}){sub 2} in a short-cut process involved merely with leaching and filtrating, under the optimized leaching conditions of 40 °C (T), 60 min (t), 4 vol.% H{sub 2}O{sub 2}, 20 mL g{sup −1} (L/S) and 0.7 mol/L H{sub 3}PO{sub 4}. Then leaching kinetics was investigated based on the logarithmic rate kinetics model and the obtained results indicate that the leaching of Co and Li fits well with this model and the activation energies (Ea) for Co and Li are 7.3 and 10.2 kJ/mol, respectively. Finally, it can be discovered from characterization results that the obtained product is 97.1% pure cobalt phosphate (Co{sub 3}(PO{sub 4}){sub 2}).

  6. Enhanced recovery of valuable metals from spent lithium-ion batteries through optimization of organic acids produced by Aspergillus niger.

    Science.gov (United States)

    Bahaloo-Horeh, Nazanin; Mousavi, Seyyed Mohammad

    2017-02-01

    In the present study, spent medium bioleaching method was performed using organic acids produced by Aspergillus niger to dissolve Ni, Co, Mn, Li, Cu and Al from spent lithium-ion batteries (LIBs). Response surface methodology was used to investigate the effects and interactions between the effective factors of sucrose concentration, initial pH, and inoculum size to optimize organic acid production. Maximum citric acid, malic acid, and gluconic acid concentrations of 26,478, 1832.53 and 8433.76ppm, respectively, and a minimum oxalic acid concentration of 305.558ppm were obtained under optimal conditions of 116.90 (gl(-1)) sucrose concentration, 3.45% (vv(-1)) inoculum size, and a pH value of 5.44. Biogenically-produced organic acids are used for leaching of spent LIBs at different pulp densities. The highest metal recovery of 100% Cu, 100% Li, 77% Mn, and 75% Al occurred at 2% (wv(-1)) pulp density; 64% Co and 54% Ni recovery occurred at 1% (wv(-1)) pulp density. The bioleaching of metals from spent LIBs can decrease the environmental impact of this waste. The results of this study suggest that the process can be used for large scale industrial purposes. Copyright © 2016 Elsevier Ltd. All rights reserved.

  7. Succinic acid-based leaching system: A sustainable process for recovery of valuable metals from spent Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Li, Li; Qu, Wenjie; Zhang, Xiaoxiao; Lu, Jun; Chen, Renjie; Wu, Feng; Amine, Khalil

    2015-05-01

    A hydrometallurgical method involving natural organic acid leaching has been developed for recovery of lithium and cobalt from the cathode active materials in spent lithium-ion batteries. Succinic acid is employed as leaching agent and H2O2 as reductant. The cobalt and lithium contents from the succinic acid-based treatment of spent batteries are determined by inductively coupled plasma-optical emission spectroscopy to calculate the leaching efficiency. The spent LiCoO2 samples after calcination and the residues after leaching are characterized by X-ray diffraction and scanning electron microscopy. The results show that nearly 100% of cobalt and more than 96% of lithium are leached under optimal conditions: succinic acid concentration of 1.5 mol L-1, H2O2 content of 4 vol.%, solid-to-liquid ratio of 15 g L-1, temperature of 70 °C, and reaction time of 40 min. Results are also given for fitting of the experimental data to acid leaching kinetic models.

  8. Recovery of valuable metals from industrial wastes

    Directory of Open Access Journals (Sweden)

    A. K. Serikbayeva

    2013-10-01

    Full Text Available Recovery of valuable metals as osmium and rhenium from a industrial wastes are an actual problem. A wastes of copper production treat slime and cake. The content of rhenium in them makes 600 – 2 000 g/t, osmium to 50 g/t. In article results of research of a form of finding of osmium and rhenium in such waste and influence phase transformation of the main components on their extraction when processing are stated. The probable reactions, proceeding in this system are provided. The way of receiving enriched with osmium and rhenium of concentrates from a waste is offered.

  9. Technologies for Extracting Valuable Metals and Compounds from Geothermal Fluids

    Energy Technology Data Exchange (ETDEWEB)

    Harrison, Stephen [SIMBOL Materials

    2014-04-30

    Executive Summary Simbol Materials studied various methods of extracting valuable minerals from geothermal brines in the Imperial Valley of California, focusing on the extraction of lithium, manganese, zinc and potassium. New methods were explored for managing the potential impact of silica fouling on mineral extraction equipment, and for converting silica management by-products into commercial products.` Studies at the laboratory and bench scale focused on manganese, zinc and potassium extraction and the conversion of silica management by-products into valuable commercial products. The processes for extracting lithium and producing lithium carbonate and lithium hydroxide products were developed at the laboratory scale and scaled up to pilot-scale. Several sorbents designed to extract lithium as lithium chloride from geothermal brine were developed at the laboratory scale and subsequently scaled-up for testing in the lithium extraction pilot plant. Lithium The results of the lithium studies generated the confidence for Simbol to scale its process to commercial operation. The key steps of the process were demonstrated during its development at pilot scale: 1. Silica management. 2. Lithium extraction. 3. Purification. 4. Concentration. 5. Conversion into lithium hydroxide and lithium carbonate products. Results show that greater than 95% of the lithium can be extracted from geothermal brine as lithium chloride, and that the chemical yield in converting lithium chloride to lithium hydroxide and lithium carbonate products is greater than 90%. The product purity produced from the process is consistent with battery grade lithium carbonate and lithium hydroxide. Manganese and zinc Processes for the extraction of zinc and manganese from geothermal brine were developed. It was shown that they could be converted into zinc metal and electrolytic manganese dioxide after purification. These processes were evaluated for their economic potential, and at the present time Simbol

  10. Adsorption of valuable metals from leachates of mobile phone wastes using biopolymers and activated carbon.

    Science.gov (United States)

    Zazycki, Maria A; Tanabe, Eduardo H; Bertuol, Daniel A; Dotto, Guilherme L

    2017-03-01

    In this work, chitin (CTN), chitosan (CTS) and activated carbon (AC) were used as adsorbents to recover valuable metals from leachates of mobile phone wastes. The mobile phone wastes (contactors) were collected and characterized. The valuable metals were extracted by thiourea leaching. The adsorption of valuable metals from leachates was studied according to the kinetic and equilibrium viewpoints. It was found that the contactors were composed by Au, Ni, Cu and Sn. The thiourea leaching provided extraction percentages of 68.6% for Au, 22.1% for Ni and 2.8% for Cu. Sn was not extracted. The leachate presented 17.5 mg L-1 of Au, 324.9 mg L-1 of Ni and 573.1 mg L-1 of Cu. The adsorption was fast, being the equilibrium attained within 120 min. The adsorption of Au, Ni and Cu onto CTN and AC followed the Langmuir model, while, the adsorption of these metals onto CTS, followed the Freundlich model. Removal percentages higher than 95% were obtained for all metals, depending of the type and amount of adsorbent. It was demonstrated that the adsorption onto chitin, chitosan and activated carbon can be an alternative to recover valuable metals from leachates of mobile phone wastes. Copyright © 2016 Elsevier Ltd. All rights reserved.

  11. Effect of Acid Dissolution Conditions on Recovery of Valuable Metals from Used Plasma Display Panel Scrap

    Directory of Open Access Journals (Sweden)

    Kim Chan-Mi

    2017-06-01

    Full Text Available The objective of this particular study was to recover valuable metals from waste plasma display panels using high energy ball milling with subsequent acid dissolution. Dissolution of milled (PDP powder was studied in HCl, HNO3, and H2SO4 acidic solutions. The effects of dissolution acid, temperature, time, and PDP scrap powder to acid ratio on the leaching process were investigated and the most favorable conditions were found: (1 valuable metals (In, Ag, Mg were recovered from PDP powder in a mixture of concentrated hydrochloric acid (HCl:H2O = 50:50; (2 the optimal dissolution temperature and time for the valuable metals were found to be 60°C and 30 min, respectively; (3 the ideal PDP scrap powder to acid solution ratio was found to be 1:10. The proposed method was applied to the recovery of magnesium, silver, and indium with satisfactory results.

  12. Deep cleaning of a metallurgical zinc leaching residue and recovery of valuable metals

    Science.gov (United States)

    Xing, Peng; Ma, Bao-zhong; Zeng, Peng; Wang, Cheng-yan; Wang, Ling; Zhang, Yong-lu; Chen, Yong-qiang; Wang, Shuo; Wang, Qiu-yin

    2017-11-01

    Huge quantities of zinc leaching residues (ZLRs) generated from zinc production are dumped continuously around the world and pose a potential environmental threat because of their considerable amounts of entrained heavy metals (mainly lead). Most ZLRs have not been properly treated and the valuable metals in them have not yet been effectively recovered. Herein, the deep cleaning of a ZLR and recovery of valuable metals via a hydrometallurgical route were investigated. The cleaning process consists of two essential stages: acid leaching followed by calcium chloride leaching. The optimum conditions for extracting zinc, copper, and indium by acid leaching were a sulfuric acid concentration of 200 g·L-1, a liquid/solid ratio of 4:1 (mL/g), a leaching time of 2 h, and a temperature of 90°C. For lead and silver extractions, the optimum conditions were a calcium chloride concentration of 400 g·L-1, a pH value of 1.0, a leaching time of 1 h, and a temperature of 30°C. After calcium chloride leaching, silver and lead were extracted out and the lead was finally recovered as electrolytic lead by electrowinning. The anglesite phase, which poses the greatest potential environmental hazard, was removed from the ZLR after deep cleaning, thus reducing the cost of environmental management of ZLRs. The treatment of chlorine and spent electrolyte generated in the process was discussed.

  13. Energetical fly ashes – separation and utilization of metallic valuable components

    Directory of Open Access Journals (Sweden)

    Michalíková Františka

    2000-12-01

    Full Text Available In the contribution, methods of separating metals – Fe, Al, Ge from energetic wastes – fly ashes are presented along with further possibilities of utilization of particular valuable components for industrial purposes.In the contribution, properties of energetic wastes are presented influencing the contents, separability, and utilizability of metal-bearing valuable components. From among physical properties these are grain size distribution and surface area. Chemical properties are characterized by elements contained in combusted coal whose content after combustion is increased 2 to 4 times, depending on the content of ash and combustible matters in original coal. Mineralogical properties of energetic wastes are determined by the combustion process conditions in the course of which mineral novelties are produced in concentrations suitable for separation.In the contribution, methods of separation and utilization of metals such as Fe, Al, Ge are described. From literature information on the processing of Fe component, as well as from results of experiments made at the Department of Mineral Processing and Environmental Protection, Technical University of Kosice follows that the highest concentration and mass yield of the component can be obtained from black coal fly ashes produced in smelting boilers. The content of Al in Slovak energetic wastes is lower than the 30 % Al2O3 limit that conditions an economic technological processing. Only in the case of black coal fly ash from TEKO Kosice and EVO Vojany was the Al2O3 content of 32.93 %. Therefore, in an indirect way – by separating the residues of uncombusted coal and magnetite Fe – the content of Al in fly ash was increased.For Ge, a principle of selective sizing has been utilized.A complex utilization of energetic wastes, that is the separation of metallic components, elimination of particular metals and the subsequent treatment of nonmetallic residue, should be an effective solution in various

  14. An alternative approach to recovering valuable metals from zinc phosphating sludge.

    Science.gov (United States)

    Kuo, Yi-Ming

    2012-01-30

    This study used a vitrification process (with good potential for commercialization) to recover valuable metals from Zn phosphating sludge. The involved vitrification process achieves two major goals: it transformed hazardous Zn phosphating sludge into inert slag and it concentrated Fe (83.5%) and Zn (92.8%) into ingot and fine particulate-phase material, respectively. The Fe content in the ingot was 278,000 mg/kg, making the ingot a potential raw material for iron making. The fine particulate-phase material (collected from flue gas) contained abundant Zn (544,000 mg/kg) in the form of ZnO. The content (67.7%) of ZnO was high, so it can be directly sold to refineries. The recovered coarse particulate-phase material, with insufficient amount of ZnO, can be recycled as a feeding material for Zn re-concentration. Therefore, the vitrification process can not only treat hazardous materials but also effectively recover valuable metals. Copyright © 2011 Elsevier B.V. All rights reserved.

  15. Controllable Phase Transformation in Extracting Valuable Metals from Chinese Low-Grade Nickel Sulphide Ore

    Science.gov (United States)

    Cui, Fuhui; Mu, Wenning; Wang, Shuai; Xu, Qian; Zhai, Yuchun; Luo, Shaohua

    2017-10-01

    In this work, a two-stage sulphuric acid roasting and water leaching system was chosen to extract valuable metals from Chinese low-grade nickel sulphide ore. By optimizing the two-stage roasting process, first roasting temperature at 295°C with particle size of 80-91 μm with an acid-ore ratio of 1.1:1 for 2 h, and second roasting temperature at 620°C for 2 h, it was found that more than 98% of the nickel and 99% of the copper but less than 14.38% of Fe were leached into the water. Attempts were made via x-ray diffraction analysis, scanning electron microscopy, chemical phase analysis, and differential thermal and thermogravimetric analysis to reveal the phase transformations for Ni, Cu, and Mg, which could be expressed as mineral phases → sulphates hydrate → sulphates and for iron as mineral phases → hydrated ferrous sulphate → ferric sulphates and ferric oxide → oxide. The results of this work suggest that a controllable phase transformation by using a two-stage sulphuric acid roasting process is a feasible method for efficiently extracting valuable metals from Chinese nickel sulphide ore.

  16. Recovery of valuable metals from acid mine drainage by selective titration

    Energy Technology Data Exchange (ETDEWEB)

    Jenke, D.R.; Diebold, F.E.

    1983-01-01

    Acid solutions associated with the non-ferrous metal mining industry contain economically significant amounts of heavy metals including Al, Cu, Zn, Mn and Mg. These metals are usually rendered non-recoverable by the conventional neutralization treatment technologies used to create environmentally acceptable discharge. Acid solutions which are generated as the result of the mining of a porphyry Cu deposit were subjected to laboratory scale titration sequences. When these base titrations involve appropriate initial additions of an oxidizing agent and the sulfide ion, better than 85% of the dissolved metals are sequentially separated from the solution in distinct pH regimes. These precipitates include the sulfides of Cu and Zn and the hydroxides of Fe, Al, Mn and Mg. The possibility of using specific conductance and ionic strength of the solution as a means of determining appropriate endpoints in the titration sequence is discussed. These sequential metal separations provide a means for the recovery of a substantial amount of the cost of generating an environmentally acceptable discharge.

  17. An environmentally friendly ball milling process for recovery of valuable metals from e-waste scraps.

    Science.gov (United States)

    Zhang, Zhi-Yuan; Zhang, Fu-Shen; Yao, TianQi

    2017-10-01

    The present study reports a mechanochemical (MC) process for effective recovery of copper (Cu) and precious metals (i.e. Pd and Ag) from e-waste scraps. Results indicated that the mixture of K 2 S 2 O 8 and NaCl (abbreviated as K 2 S 2 O 8 /NaCl hereafter) was the most effective co-milling reagents in terms of high recovery rate. After co-milling with K 2 S 2 O 8 /NaCl, soluble metallic compounds were produced and consequently benefit the subsequent leaching process. 99.9% of Cu and 95.5% of Pd in the e-waste particles could be recovered in 0.5mol/L diluted HCl in 15min. Ag was concentrated in the leaching residue as AgCl and then recovered in 1mol/L NH 3 solution. XRD and XPS analysis indicated that elemental metals in the raw materials were transformed into their corresponding oxidation state during ball milling process at low temperature, implying that solid-solid phase reactions is the reaction mechanism. Based on the results and thermodynamic parameters of the probable reactions, possible reaction pathways during ball milling were proposed. Suggestion on category of e-waste for ball milling process was put forward according to the experiment results. The designed metal recovery process of this study has the advantages of highly recovery rate and quick leaching speed. Thus, this study offers a promising and environmentally friendly method for recovering valuable metals from e-waste. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Metal ions, Alzheimer's disease and chelation therapy

    National Research Council Canada - National Science Library

    Budimir, Ana

    2011-01-01

    .... In contrast to the direct chelation approach in metal ion overload disorders, in neurodegeneration the goal seems to be a better and subtle modulation of metal ion homeostasis, aimed at restoring ionic balance...

  19. Leaching capacity of metals-metalloids and recovery of valuable materials from waste LCDs.

    Science.gov (United States)

    Savvilotidou, Vasiliki; Hahladakis, John N; Gidarakos, Evangelos

    2015-11-01

    The purpose of Directive 2012/19/EU which is related to WEEE (Waste Electrical and Electronic Equipment), also known as "e-waste", is to contribute to their sustainable production and consumption that would most possibly be achieved by their recovery, recycling and reuse. Under this perspective, the present study focused on the recovery of valuable materials, metals and metalloids from LCDs (Liquid Crystal Displays). Indium (In), arsenic (As) and stibium (Sb) were selected to be examined for their Leaching Capacity (R) from waste LCDs. Indium was selected mainly due to its rarity and preciousness, As due to its high toxicity and wide use in LCDs and Sb due to its recent application as arsenic's replacement to improve the optimal clarity of a LCD screen. The experimental procedure included disassembly of screens along with removal and recovery of polarizers via thermal shock, cutting, pulverization and digestion of the shredded material and finally leaching evaluation of the aforementioned elements. Leaching tests were conducted under various temperatures, using various solid:liquid (S/L) ratios and solvents (acid mixtures), to determine the optimal conditions for obtaining the maximum leaching capacities. The examined elements exhibited different leaching behaviors, mainly due to the considerable diversity in their inherent characteristic properties. Indium demonstrated the highest recovery percentages (approximately 60%), while the recovery of As and Sb was unsuccessful, obtaining poor leaching percentages (0.16% and 0.5%, respectively). Copyright © 2015 Elsevier Ltd. All rights reserved.

  20. METAL ION SEQUESTRATION: AN EXCITING DIMENSION FOR ...

    African Journals Online (AJOL)

    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 route for a targeted metal ion, with potential for environmental remediation and restoration applications. Ethylene ...

  1. 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...

  2. [Electric current around dental metals as a factor producing allergenic metal ions in the oral cavity].

    Science.gov (United States)

    Nogi, N

    1989-11-01

    to be higher than with other metals. 5) The voltages and electric currents were often higher between mucous membrane and metals than between metals. These findings indicate that the patient's own mucous membrane acts as cathode for the electrochemical dissolution rather than the dental metals. 6) Measuring the voltage and electric current in the patient's oral cavities is technically easy, and is considered to be valuable since the tendancy of electrochemical dissolution of metal ions from the dental metals is clearly demonstrated.

  3. An environmentally friendly process for the recovery of valuable metals from spent refinery catalysts.

    Science.gov (United States)

    Rocchetti, Laura; Fonti, Viviana; Vegliò, Francesco; Beolchini, Francesca

    2013-06-01

    The present study dealt with the whole valorization process of exhaust refinery catalysts, including metal extraction by ferric iron leaching and metal recovery by precipitation with sodium hydroxide. In the leaching operation the effects on metal recovery of the concentration and kind of acid, the concentration of catalyst and iron (III) were determined. The best operating conditions were 0.05 mol L(-1) sulfuric acid, 40 g L(-1) iron (III), 10% catalyst concentration; almost complete extraction of nickel and vanadium, and 50%extraction efficiency of aluminium and less than 20% for molybdenum. Sequential precipitation on the leach liquor showed that it was not possible to separate metals through such an approach and a recovery operation by means of a single-stage precipitation at pH 6.5 would simplify the procedures and give a product with an average content of iron (68%), aluminium (13%), vanadium (11%), nickel (6%) and molybdenum (1%) which would be potentially of interest in the iron alloy market. The environmental sustainability of the process was also assessed by means of life cycle assessment and yielded an estimate that the highest impact was in the category of global warming potential with 0.42 kg carbon dioxide per kg recovered metal.

  4. Metal Ion Modeling Using Classical Mechanics

    Science.gov (United States)

    2017-01-01

    Metal ions play significant roles in numerous fields including chemistry, geochemistry, biochemistry, and materials science. With computational tools increasingly becoming important in chemical research, methods have emerged to effectively face the challenge of modeling metal ions in the gas, aqueous, and solid phases. Herein, we review both quantum and classical modeling strategies for metal ion-containing systems that have been developed over the past few decades. This Review focuses on classical metal ion modeling based on unpolarized models (including the nonbonded, bonded, cationic dummy atom, and combined models), polarizable models (e.g., the fluctuating charge, Drude oscillator, and the induced dipole models), the angular overlap model, and valence bond-based models. Quantum mechanical studies of metal ion-containing systems at the semiempirical, ab initio, and density functional levels of theory are reviewed as well with a particular focus on how these methods inform classical modeling efforts. Finally, conclusions and future prospects and directions are offered that will further enhance the classical modeling of metal ion-containing systems. PMID:28045509

  5. Computational Design of Metal Ion Sequestering Agents

    Energy Technology Data Exchange (ETDEWEB)

    Hay, Benjamin P.; Rapko, Brian M.

    2006-06-01

    Organic ligands that exhibit a high degree of metal ion recognition are essential precursors for developing separation processes and sensors for metal ions. Since the beginning of the nuclear era, much research has focused on discovering ligands that target specific radionuclides. Members of the Group 1A and 2A cations (e.g., Cs, Sr, Ra) and the f-block metals (actinides and lanthanides) are of primary concern to DOE. Although there has been some success in identifying ligand architectures that exhibit a degree of metal ion recognition, the ability to control binding affinity and selectivity remains a significant challenge. The traditional approach for discovering such ligands has involved lengthy programs of organic synthesis and testing that, in the absence of reliable methods for screening compounds before synthesis, have resulted in much wasted research effort.

  6. Computational Design of Metal Ion Sequestering Agents

    Energy Technology Data Exchange (ETDEWEB)

    Hay, Benjamin P.; Rapko, Brian M.

    2005-06-15

    Organic ligands that exhibit a high degree of metal ion recognition are essential precursors for developing separation processes and sensors for metal ions. Since the beginning of the nuclear era, much research has focused on discovering ligands that target specific radionuclides. Members of the Group 1A and 2A cations (e.g., Cs, Sr, Ra) and the f-block metals (actinides and lanthanides) are of primary concern to DOE. Although there has been some success in identifying ligand architectures that exhibit a degree of metal ion recognition, the ability to control binding affinity and selectivity remains a significant challenge. The traditional approach for discovering such ligands has involved lengthy programs of organic synthesis and testing that, in the absence of reliable methods for screening compounds before synthesis, have resulted in much wasted research effort.

  7. Recovery of valuable metals from electronic scraps by clays and organo-clays: Study on bi-ionic model solutions.

    Science.gov (United States)

    Iannicelli-Zubiani, Elena Maria; Cristiani, Cinzia; Dotelli, Giovanni; Gallo Stampino, Paola

    2017-02-01

    The demand of valuable metals, as precious metals and rare earths, is constantly increasing in the global market, as many and different technological applications exploit these materials because of their unique properties. Since natural resources are located just in focused areas, an interesting possibility could be the recovery of metals from Waste Electrical and Electronic Equipment (WEEE). The aim of this work is to evaluate the recovery potentialities of clays and organo-clay based systems towards the metals contained in the solutions of electronic scraps dissolved in strong acid, by preliminary tests on bi-ionic model solutions. Lanthanum has been chosen as representative of the rare earths while copper has been considered since it is by far the most used metal in electric and electronic equipment. The considered sorbents are a montmorillonitic clay and two polyamine based organo-clays. Uptake and release processes have been carried out in order to assess the performances of these solids and to evaluate the uptake and release mechanisms. The results showed that the cationic exchange is the prevailing mechanism in the case of pristine clay, while both coordinating effect due to amino groups and cationic exchange occur in the case of modified clays, respectively accounting for copper and lanthanum uptake. Furthermore the pH was found having a great influence in both the adsorption and desorption phenomena. Copyright © 2016 Elsevier Ltd. All rights reserved.

  8. Computational Design of Metal Ion Sequestering Agents

    Energy Technology Data Exchange (ETDEWEB)

    Hay, Benjamin P.; Rapko, Brian M.

    2005-06-15

    Organic ligands that exhibit a high degree of metal ion recognition are essential precursors for developing separation processes and sensors for metal ions. Since the beginning of the nuclear era, much research has focused on discovering ligands that target specific radionuclides. Members of the Group 1A and 2A cations (e.g., Cs, Sr, Ra) and the f-block metals (actinides and lanthanides) are of primary concern to DOE. Although there has been some success in identifying ligand architectures that exhibit a degree of metal ion recognition, the ability to control binding affinity and selectivity remains a significant challenge. The traditional approach for discovering such ligands has involved lengthy programs of organic synthesis and testing that, in the absence of reliable methods for screening compounds before synthesis, have resulted in much wasted research effort. This project seeks to enhance and strengthen the traditional approach through computer-aided design of new and improved host molecules. Accurate electronic structure calculations are coupled with experimental data to provide fundamental information about ligand structure and the nature of metal-donor group interactions (design criteria). This fundamental information then is used in a molecular mechanics model (MM) that helps us rapidly screen proposed ligand architectures and select the best members from a set of potential candidates. By using combinatorial methods, molecule building software has been developed that generates large numbers of candidate architectures for a given set of donor groups. The specific goals of this project are: • further understand the structural and energetic aspects of individual donor group- metal ion interactions and incorporate this information within the MM framework • further develop and evaluate approaches for correlating ligand structure with reactivity toward metal ions, in other words, screening capability • use molecule structure building software to generate

  9. 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.

  10. Metal ion levels and lymphocyte counts

    DEFF Research Database (Denmark)

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

    2013-01-01

    BACKGROUND AND PURPOSE: Wear particles from metal-on-metal arthroplasties are under suspicion for adverse effects both locally and systemically, and the DePuy ASR Hip Resurfacing System (RHA) has above-average failure rates. We compared lymphocyte counts in RHA and total hip arthroplasty (THA....../ppb. INTERPRETATION: Circulating T-lymphocyte levels may decline after surgery, regardless of implant type. Metal ions-particularly cobalt-may have a general depressive effect on T- and B-lymphocyte levels. Registered with ClinicalTrials.gov under # NCT01113762....

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

    African Journals Online (AJOL)

    Preferred Customer

    their tendency to undergo electrochemical corrosion while in contact with physiological fluids. The electrochemical reaction resulting to the release of metal ions is coupled with a corresponding reduction reaction of constituents in the aqueous environment to maintain charge neutrality [3]. The oral cavity is warm and damp, ...

  12. Metal ions and human sperm mannose receptors.

    Science.gov (United States)

    Benoff, S; Cooper, G W; Centola, G M; Jacob, A; Hershlag, A; Hurley, I R

    2000-09-01

    Zinc and lead concentrations were measured in seminal plasma from fertile donors, infertile men with varicocoele and men undergoing work-ups for in vitro fertilization. Ejaculated spermatozoa from these subjects were incubated in vitro with various metal ions and/or dibromoethane and dibromochloropropane. Mannose receptor expression was correlated with metal and toxicant levels. Sperm distributions of potassium channels were compared with lead ions and calcium channels with zinc ions. Mannose receptor expression by capacitated spermatozoa increased linearly with seminal plasma zinc levels, and correlated inversely with lead levels. Cobalt had no effect on mannose receptor expression, but nickel had a concentration-dependent biphasic effect. Mannose receptor expression was not affected by dibromoethane and dibromochloropropane if the cholesterol content of the sperm membrane was high, but mannose receptor expression was decreased in low cholesterol spermatozoa by exposures below estimated permissive exposure limits. Potassium channels and lead ions co-localized over the entire head of human spermatozoa, while both calcium channels and zinc ions were confined to the equatorial segment of the head. Mannose receptor expression on the external surface of the human sperm plasma membrane is a biomarker for the effects of transition and heavy metals and organic toxicants on sperm fertility potential.

  13. Uncoupling metallonuclease metal ion binding sites via nudge mutagenesis.

    Science.gov (United States)

    Papadakos, Grigorios A; Nastri, Horacio; Riggs, Paul; Dupureur, Cynthia M

    2007-05-01

    The hydrolysis of phosphodiester bonds by nucleases is critical to nucleic acid processing. Many nucleases utilize metal ion cofactors, and for a number of these enzymes two active-site metal ions have been detected. Testing proposed mechanistic roles for individual bound metal ions has been hampered by the similarity between the sites and cooperative behavior. In the homodimeric PvuII restriction endonuclease, the metal ion dependence of DNA binding is sigmoidal and consistent with two classes of coupled metal ion binding sites. We reasoned that a conservative active-site mutation would perturb the ligand field sufficiently to observe the titration of individual metal ion binding sites without significantly disturbing enzyme function. Indeed, mutation of a Tyr residue 5.5 A from both metal ions in the enzyme-substrate crystal structure (Y94F) renders the metal ion dependence of DNA binding biphasic: two classes of metal ion binding sites become distinct in the presence of DNA. The perturbation in metal ion coordination is supported by 1H-15N heteronuclear single quantum coherence spectra of enzyme-Ca(II) and enzyme-Ca(II)-DNA complexes. Metal ion binding by free Y94F is basically unperturbed: through multiple experiments with different metal ions, the data are consistent with two alkaline earth metal ion binding sites per subunit of low millimolar affinity, behavior which is very similar to that of the wild type. The results presented here indicate a role for the hydroxyl group of Tyr94 in the coupling of metal ion binding sites in the presence of DNA. Its removal causes the affinities for the two metal ion binding sites to be resolved in the presence of substrate. Such tuning of metal ion affinities will be invaluable to efforts to ascertain the contributions of individual bound metal ions to metallonuclease function.

  14. Material Removes Heavy Metal Ions From Water

    Science.gov (United States)

    Philipp, Warren H., Jr.; Street, Kenneth W.; Hill, Carol; Savino, Joseph M.

    1995-01-01

    New high capacity ion-exchange polymer material removes toxic metal cations from contaminated water. Offers several advantages. High sensitivities for such heavy metals as lead, cadmium, and copper and capable of reducing concentrations in aqueous solutions to parts-per-billion range. Removes cations even when calcium present. Material made into variety of forms, such as thin films, coatings, pellets, and fibers. As result, adapted to many applications to purify contaminated water, usually hard wherever found, whether in wastewater-treatment systems, lakes, ponds, industrial plants, or homes. Another important feature that adsorbed metals easily reclaimed by either destructive or nondestructive process. Other tests show ion-exchange polymer made inexpensively; easy to use; strong, flexible, not easily torn; and chemically stable in storage, in aqueous solutions, and in acidic or basic solution.

  15. Metal ions affecting reproduction and development.

    Science.gov (United States)

    Apostoli, Pietro; Catalani, Simona

    2011-01-01

    Many metal ions (lead, mercury, arsenic, cadmium, chromium, nickel, vanadium, copper, lithium) exert a wide variety of adverse effects on reproduction and development, including influence on male and female subfertility or fertility, abortions, malformations, birth defects, and effects on the central nervous system. The effects produced by metal ions depend on several factors, such as timing and duration of exposure, their distribution and accumulation in various organs (e.g., the nervous system), and on the interference with specific developmental processes. Neonatal and early postnatal periods are lifespan segments during which sensitivity to metals is high; e.g., lead toxicity on the developing organism is paradigmatic of related well known and still open questions. In more recent decades, important mechanisms of action have been suggested: the endocrine disruption via impact of metal ions on reproductive hormones and the oxidative stress. While experimental data provide clear evidence of effects of many metals, human data are scant and traditionally limited to high levels of a few metal ions, like lead on male fertility. Less documented are reproductive effects for mercury, manganese, chromium, nickel, and arsenic for the same gender. More complex is the demonstration of effects on female reproduction and on pregnancy. The action of lead, arsenic, cadmium, chromium, and mercury may in fact be relevant in several stages, beginning in fetal life, during early development or maturity, and is characterized by subfertility, infertility, intrauterine growth retardation, spontaneous abortions, malformations, birth defects, postnatal death, learning and behavior deficits, and premature aging. Also, for females the evidences of specific aspects such as fertility or abortions are usually higher and clearer from animal experiments than from human studies.

  16. Harnessing Aggregation-Induced Emission (aie) of Tetraphenylethylenes in Metal Ion Sensing and Luminescent Metal-Organic Frameworks

    Science.gov (United States)

    Pigge, F. Christopher

    2013-08-01

    Tetraphenylethylene derivatives have emerged as valuable building blocks for construction of luminescent molecular sensor materials based on their ability to display aggregation induced emission. This paper summarizes recent efforts aimed at combining the luminescent properties of tetraphenylethylenes with metal ligating capability as a means to achieve metal ion detection. Research describing the incorporation of tetraphenylethylene ligands in metal-organic frameworks is also discussed. Though these areas of investigation have not received a great deal of attention, metal coordination complexes of tetraphenylethylenes show tremendous promise as switchable fluorescent sensors/indicators with a variety of potential applications.

  17. 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 ...

  18. 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 Bi 2 + ions at room temperature from a GaBi capillary LMAIS will be presented and discussed.

  19. 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 ...

  20. Synthesis and characterization of metal ion imprinted polymers

    Indian Academy of Sciences (India)

    57

    ABSTRACT. In this study, ion-imprinted polymeric materials to remove metal ions (M2+) like Ni2+, Co2+ etc from an aqueous solution were prepared. To prepare ion-imprinted polymers, acrylic acid derivatives. (XA) like acrylamide (AAm) and methacrylic, itaconic acid were chosen as monomer. Metal ions formed binary ...

  1. Transporters of ligands for essential metal ions in plants.

    Science.gov (United States)

    Haydon, Michael J; Cobbett, Christopher S

    2007-01-01

    Essential metals are required for healthy plant growth but can be toxic when present in excess. Therefore plants have mechanisms of metal homeostasis which involve coordination of metal ion transporters for uptake, translocation and compartmentalization. However, very little metal in plants is thought to exist as free ions. A number of small, organic molecules have been implicated in metal ion homeostasis as metal ion ligands to facilitate uptake and transport of metal ions with low solubility and also as chelators implicated in sequestration for metal tolerance and storage. Ligands for a number of essential metals have been identified and proteins involved in the transport of these ligands and of metal-ligand complexes have been characterized. Here we review recent advances in understanding the role of mugineic acid, nicotianamine, organic acids (citrate and malate), histidine and phytate as ligands for iron (Fe), zinc (Zn), copper (Cu), manganese (Mn) and nickel (Ni) in plants, and the proteins identified as their transporters.

  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. Separation of traces of metal ions from sodium matrices

    Science.gov (United States)

    Korkisch, J.; Orlandini, K. A.

    1969-01-01

    Method for isolating metal ion traces from sodium matrices consists of two extractions and an ion exchange step. Extraction is accomplished by using 2-thenoyltrifluoracetone and dithizone followed by cation exchange.

  5. 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.

  6. Plasma-based ion implantation: a valuable technology for the elaboration of innovative materials and nanostructured thin films

    Science.gov (United States)

    Vempaire, D.; Pelletier, J.; Lacoste, A.; Béchu, S.; Sirou, J.; Miraglia, S.; Fruchart, D.

    2005-05-01

    Plasma-based ion implantation (PBII), invented in 1987, can now be considered as a mature technology for thin film modification. After a brief recapitulation of the principle and physics of PBII, its advantages and disadvantages, as compared to conventional ion beam implantation, are listed and discussed. The elaboration of thin films and the modification of their functional properties by PBII have already been achieved in many fields, such as microelectronics (plasma doping/PLAD), biomaterials (surgical implants, bio- and blood-compatible materials), plastics (grafting, surface adhesion) and metallurgy (hard coatings, tribology), to name a few. The major advantages of PBII processing lie, on the one hand, in its flexibility in terms of ion implantation energy (from 0 to 100 keV) and operating conditions (plasma density, collisional or non-collisional ion sheath), and, on the other hand, in the easy transferrability of processes from the laboratory to industry. The possibility of modifying the composition and physical nature of the films, or of drastically changing their physical properties over several orders of magnitude makes this technology very attractive for the elaboration of innovative materials, including metastable materials, and the realization of micro- or nanostructures. A review of the state of the art in these domains is presented and illustrated through a few selected examples. The perspectives opened up by PBII processing, as well as its limitations, are discussed.

  7. The charge state of hydrogen ions in metals and semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Bazhukov, S.I.; Kibardin, A.V.; Pyatkova, T.M.; Urmanov, A.R. (Urals Polytechnical Inst., Sverdlovsk (USSR))

    1991-06-01

    The charge state of hydrogen ions in metals and semiconductors has been studied based on a comparison of hydrogen ion stopping cross-sections in metal and semiconductor targets. It is shown that neutralization of the hydrogen ion in metals and semiconductors at ion speeds v{sub i} {proportional to} (1-2)v{sub 0}, where v{sub 0} = 2.2x10{sup 8} cm/s, is due to different mechanisms, i.e. to a bulk effect in metals and to a subsurface effect in semiconductors. (orig.).

  8. Structure simulation into a lamellar supramolecular network and calculation of the metal ions/ligands ratio

    Directory of Open Access Journals (Sweden)

    Visa Aurelia

    2012-08-01

    Full Text Available Abstract Background Research interest in phosphonates metal organic frameworks (MOF has increased extremely in the last two decades, because of theirs fascinating and complex topology and structural flexibility. In this paper we present a mathematical model for ligand/metal ion ratio of an octahedral (Oh network of cobalt vinylphosphonate (Co(vP·H2O. Results A recurrent relationship of the ratio between the number of ligands and the number of metal ions in a lamellar octahedral (Oh network Co(vP·H2O, has been deducted by building the 3D network step by step using HyperChem 7.52 package. The mathematical relationship has been validated using X ray analysis, experimental thermogravimetric and elemental analysis data. Conclusions Based on deducted recurrence relationship, we can conclude prior to perform X ray analysis, that in the case of a thermogravimetric analysis pointing a ratio between the number of metal ions and ligands number around 1, the 3D network will have a central metal ion that corresponds to a single ligand. This relation is valid for every type of supramolecular network with divalent metal central ion Oh coordinated and bring valuable information with low effort and cost.

  9. Highly charged Arq+ ions interacting with metals

    Science.gov (United States)

    Wang, Jijin; Zhang, Jian; Gu, Jiangang; Luo, Xianwen; Hu, Bitao

    2009-12-01

    Using computer simulation, alternative methods of the interaction of highly charged ions Arq+ with metals (Au, Ag) are used and verified in the present work. Based on the classical over-barrier model, we discussed the promotion loss and peeling off processes. The simulated total potential electron yields agree well with the experiment data in incident energy ranging from 100 eV to 5 keV and all charge states of Arq+ . Based on the TRIM code, we obtain the side-feeding rate as well as the motion and charge transfer of HCI below the surface. Some results, including the array of KLx x-ray satellite lines, the respective contribution of autoionization, and side-feeding to inner shells, and the filling rates and lifetime of inner shells for Ar agree well with experiment or theory.

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

    Indian Academy of Sciences (India)

    Unknown

    thus become unavailable for fluorescence quenching. In other words, in this approach, the metal ion-receptor interaction has been increased to reduce indirectly the undesired communication between the metal ion and fluorophore that leads to fluorescence quench- ing. While the above approach is indeed an elegant one, ...

  11. 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

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

    African Journals Online (AJOL)

    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 route for a targeted metal ion, with potential for environmental remediation and restoration applications. Ethylene glycol ...

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

    African Journals Online (AJOL)

    Waste materials like fruit and vegetable refuses were utilized as component of sensors capable of detecting heavy metals like lead ions and mercury ions by electrochemical method. The ability of the fabricated sensors to detect the presence of heavy metals was analyzed using electrochemical methods like cyclic ...

  14. Metal ion binding to peptides: Oxygen or nitrogen sites?

    NARCIS (Netherlands)

    Dunbar, R. C.; Polfer, N. C.; G. Berden,; Oomens, J.

    2012-01-01

    Infrared multiple-photon dissociation (IRMPD) spectroscopy was used to probe the conformations of gas-phase metal-ion complexes between a series of five metal ions and six small peptide ligands. This report is presented in recognition and tribute for the Armentrout group's long and hugely

  15. Metal ion binding to peptides: oxygen or nitrogen sites?

    NARCIS (Netherlands)

    Dunbar, R.C.; Polfer, N.C.; Berden, G.; Oomens, J.

    2012-01-01

    Infrared multiple-photon dissociation (IRMPD) spectroscopy was used to probe the conformations of gas-phase metal-ion complexes between a series of five metal ions and six small peptide ligands. This report is presented in recognition and tribute for the Armentrout group's long and hugely productive

  16. 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.

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

    African Journals Online (AJOL)

    A pseudo-second order kinetic model was used to characterize the metal ion transport mechanism and the correlation coefficients (r2) were high, confirming the validity of pseudosecond- order. The rate of adsorption was observed to increase with pillaring and does not only depend on the the metal ion concentration, but ...

  18. 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 ...

  19. 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 ...

  20. Neutralization by Metal Ions of the Toxicity of Sodium Selenide

    OpenAIRE

    Marc Dauplais; Myriam Lazard; Sylvain Blanquet; Pierre Plateau

    2013-01-01

    International audience; 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...

  1. Analysis of metal ion release from biomedical implants

    Directory of Open Access Journals (Sweden)

    Ivana Dimić

    2013-06-01

    Full Text Available Metallic biomaterials are commonly used for fixation or replacement of damaged bones in the human body due to their good combination of mechanical properties. The disadvantage of metals as implant materials is their susceptibility to corrosion and metal ion release, which can cause serious health problems. In certain concentrations metals and metal ions are toxic and their presence can cause diverse inflammatory reactions, genetic mutations or even cancer. In this paper, different approaches to metal ion release examination, from biometallic materials sample preparation to research results interpretation, will be presented. An overview of the analytical techniques, used for determination of the type and concentration of released ions from implants in simulated biofluids, is also given in the paper.

  2. DNA as Sensors and Imaging Agents for Metal Ions

    Science.gov (United States)

    Xiang, Yu

    2014-01-01

    Increasing interests in detecting metal ions in many chemical and biomedical fields have 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 attaching 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 detections. These sensors are highly sensitive (with 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 discs, 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. PMID:24359450

  3. Predictive factors for metal ion levels in metal-on-metal total hip arthroplasty.

    Science.gov (United States)

    Kasparek, Maximilian F; Renner, Lisa; Faschingbauer, Martin; Waldstein, Wenzel; Weber, Michael; Boettner, Friedrich

    2018-02-01

    Although metal-on-metal (MoM) total hip arthroplasty (THA) and hip resurfacings (HR) have similar bearing surfaces and comparable wear rates, metal ion levels and risk of failure are higher for MoM-THA. The mechanism behind the increased metal ion levels in large head MoM-THA is not completely understood. The current study aims to identify predictive factors for increased metal ion levels in unilateral and bilateral large head MoM-THA. 99 Birmingham modular MoM-THA in 87 patients with metal ion levels at least 36 months after index procedure were analyzed. Mean follow-up time was 61.3 months (range 37-108) and the relationship of the following variables (gender, age, BMI, follow-up time, UCLA Activity Score, cup inclination, femoral head size, bilateral surgery) on metal ion levels were analyzed with multivariate regression models. Multivariate regression analysis revealed that bilateral MoM-THA surgery (p MoM-THA (p = 0.004) were positively correlated with chromium levels. Positive independent predictors for the cobalt-chromium ratio in the multivariate analysis were overall follow-up time (p = 0.004), bilateral MoM-THA (p MoM-THA, increased patient activity levels and female gender are associated with increased chromium levels. Patients with larger component size, longer follow-up time and bilateral MoM-THAs have an increased cobalt-chromium ratio. These patients might be at increased risk for adverse local soft tissue reactions secondary to corrosion. Continuous close monitoring is recommended and bearing-surface change should be discussed if local tissue reactions occur.

  4. Preparation of Dithizone Functionalized Polystyrene for Detecting Heavy Metal Ion

    Energy Technology Data Exchange (ETDEWEB)

    Shin, Hyeon Ho; Kim, Younghun [Kwangwoon University, Seoul (Korea, Republic of)

    2015-04-15

    Colorimetric sensors were usually used to detect specific metal ions using selective color change of solutions. While almost organic dye in colorimetric sensors detected single molecule, dithizone (DTZ) solution could be separately detected above 5 kinds of heavy metal ions by the change of clear color. Namely, DTZ could be used as multicolorimetric sensors. However, DTZ was generally used as aqueous type and paper/pellet-type DTZ was not reported yet. Therefore, in this work, polystyrene (PS) was prepared to composite with DTZ and then DTZ/PS pellet was obtained, which was used to selectively detect 10 kinds of heavy metal ions. When 10 ppm of Hg and Co ions was exposed in DTZ/PS pellets, clear color change was revealed. It is noted that DTZ/PS pellet could be used in detecting of heavy metal ion as dry type.

  5. Role of Aspergillus niger in recovery enhancement of valuable metals from produced red mud in Bayer process.

    Science.gov (United States)

    Vakilchap, F; Mousavi, S M; Shojaosadati, S A

    2016-10-01

    Annual worldwide growth rate of red mud (RM) as a hazardous waste has caused serious environmental problems for its disposal in the mining and metallurgy industries. Accordingly, the aim of this study was to investigate biological leaching of RM and recovery of metals using organic acids exerted by Aspergillus niger. Experiments using A. niger were conducted in batch cultures with a pulp density of 2% (w/v) RM under one-step, two-step and spent-medium bioleaching. Based on HPLC results, the major lixiviant was the secretion of organic acids (citric, gluconic, oxalic and malic) by A. niger. Leaching efficiency of metals in the one-step process was the highest and the amounts of leached metals were 69.8%, 60% and 25.4% for Al, Ti and Fe, respectively. The fungal leaching technique demonstrated an adequate recovery of metals, with an efficient and cost-effective means and respect to a reuse of RM for economic and environmental purposes. Copyright © 2016 Elsevier Ltd. All rights reserved.

  6. 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.

  7. Catalysis using hydrous metal oxide ion exchangers

    Science.gov (United States)

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

    1983-07-21

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

  8. 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

  9. Bioinorganic Chemistry of the Alkali Metal Ions.

    Science.gov (United States)

    Kim, Youngsam; Nguyen, Thuy-Tien T; Churchill, David G

    2016-01-01

    The common Group 1 alkali metals are indeed ubiquitous on earth, in the oceans and in biological systems. In this introductory chapter, concepts involving aqueous chemistry and aspects of general coordination chemistry and oxygen atom donor chemistry are introduced. Also, there are nuclear isotopes of importance. A general discussion of Group 1 begins from the prevalence of the ions, and from a comparison of their ionic radii and ionization energies. While oxygen and water molecule binding have the most relevance to biology and in forming a detailed understanding between the elements, there is a wide range of basic chemistry that is potentially important, especially with respect to biological chelation and synthetic multi-dentate ligand design. The elements are widely distributed in life forms, in the terrestrial environment and in the oceans. The details about the workings in animal, as well as plant life are presented in this volume. Important biometallic aspects of human health and medicine are introduced as well. Seeing as the elements are widely present in biology, various particular endogenous molecules and enzymatic systems can be studied. Sodium and potassium are by far the most important and central elements for consideration. Aspects of lithium, rubidium, cesium and francium chemistry are also included; they help in making important comparisons related to the coordination chemistry of Na(+) and K(+). Physical methods are also introduced.

  10. 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.

  11. 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.

  12. Wastewater treatment from ions of heavy and non-ferrous metals by ion-exchange adsorption

    Directory of Open Access Journals (Sweden)

    Sevara Babazhanova

    2016-12-01

    Full Text Available This article presents the results of experimental research on wastewater treatment from ions of heavy and non-ferrous metals by ion exchange adsorption. The object of investigation was a model solution containing ions of heavy and non-ferrous metals and prepared of wastewater from Turkestan locomotive depot. As a sorbent, phosphorus–acidic cationite KRF-10P was used. The impact of the cation exchanger mass, reaction time of cationite and temperature of the solution on the degree of wastewater treatment from ions of heavy and non-ferrous metals (Zn2+, Pb2+, Cd2+ were studied. On the basis of experiments, optimal conditions of wastewater treatment from ions of heavy and non-ferrous metals were established: mKRF-10P = 2.0 g, t = 1.0 h, T = 55°C. At the optimized conditions, the degree of wastewater treatment from zinc ions reached 96.1%, the degree of removal of lead ions reached 89%, the degree of removal of cadmium ions reached 95%. Experimental results showed the possibility of wastewater treatment from ions of heavy and nonferrous metals by ion exchange adsorption using phosphorus–acidic cationite KRF-10P.

  13. Polysiloxane based CHEMFETs for the detection of heavy metal ions

    NARCIS (Netherlands)

    Lugtenberg, R.J.W.; Antonisse, M.M.G.; Egberink, Richard J.M.; Engbersen, Johannes F.J.; Reinhoudt, David

    1996-01-01

    The development of polysiloxane based chemically modified field effect transistors (CHEMFETs) for heavy metal ions is described. Different polar siloxane copolymers have been synthesized via an anionic copolymerization of hexamethylcyclotrisiloxane,

  14. An engineered palette of metal ion quenchable fluorescent proteins

    National Research Council Canada - National Science Library

    Yu, Xiaozhen; Strub, Marie-Paule; Barnard, Travis J; Noinaj, Nicholas; Piszczek, Grzegorz; Buchanan, Susan K; Taraska, Justin W

    2014-01-01

    .... With these sensors, changes in fluorescence report on chemical states in living cells. Transition metal ions such as copper, nickel, and zinc are crucial in many physiological and pathophysiological pathways...

  15. Metallic glass as a temperature sensor during ion plating

    Science.gov (United States)

    Miyoshi, K.; Spalvins, T.; Buckley, D. H.

    1985-01-01

    The temperature of the interface and/or a superficial layer of a substrate during ion plating was investigated using a metallic glass of the composition Fe67Co18B14Si1 as the substrate and as the temperature sensor. Transmission electron microscopy and diffraction studies determined the microstructure of the ion-plated gold film and the substrate. Results indicate that crystallization occurs not only in the film, but also in the substrate. The grain size of crystals formed during ion plating was 6 to 60 nm in the gold film and 8 to 100 nm in the substrate at a depth of 10 to 15 micrometers from the ion-plated interface. The temperature rise of the substrate during ion plating was approximately 500 C. Discontinuous changes in metallurgical microstructure, and physical, chemical, and mechanical properties during the amorphous to crystalline transition in metallic glasses make metallic glasses extremely useful materials for temperature sensor applications in coating processes.

  16. 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.

  17. Smart textile device using ion polymer metal compound.

    Science.gov (United States)

    Nakamura, Taro; Ihara, Tadashi

    2013-01-01

    We have developed a smart textile device that detects angular displacement of attached surface using ion polymer metal compound. The device was composed of ion polymer metal compound (IPMC) which was fabricated from Nafion resin by heat-press and chemical gold plating. The generated voltage from IPMC was measured as a function of bending angle. Fabricated IPMC device was weaved into a cotton cloth and multidirectional movements were detected.

  18. [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.

  19. A Cleaner Process for Selective Recovery of Valuable Metals from Electronic Waste of Complex Mixtures of End-of-Life Electronic Products.

    Science.gov (United States)

    Sun, Zhi; Xiao, Y; Sietsma, J; Agterhuis, H; Yang, Y

    2015-07-07

    In recent years, recovery of metals from electronic waste within the European Union has become increasingly important due to potential supply risk of strategic raw material and environmental concerns. Electronic waste, especially a mixture of end-of-life electronic products from a variety of sources, is of inherently high complexity in composition, phase, and physiochemical properties. In this research, a closed-loop hydrometallurgical process was developed to recover valuable metals, i.e., copper and precious metals, from an industrially processed information and communication technology waste. A two-stage leaching design of this process was adopted in order to selectively extract copper and enrich precious metals. It was found that the recovery efficiency and extraction selectivity of copper both reached more than 95% by using ammonia-based leaching solutions. A new electrodeposition process has been proven feasible with 90% current efficiency during copper recovery, and the copper purity can reach 99.8 wt %. The residue from the first-stage leaching was screened into coarse and fine fractions. The coarse fraction was returned to be releached for further copper recovery. The fine fraction was treated in the second-stage leaching using sulfuric acid to further concentrate precious metals, which could achieve a 100% increase in their concentrations in the residue with negligible loss into the leaching solution. By a combination of different leaching steps and proper physical separation of light materials, this process can achieve closed-loop recycling of the waste with significant efficiency.

  20. 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.

  1. 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 ...

  2. 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.

  3. Adsorption of strontium (II) metal ions using phosphonate ...

    Indian Academy of Sciences (India)

    tium (II) metal ion recovery using diethylallylphosphonate as staring material. .... gold nanoparticles, used as an active catalyst for breaking the double bond of alkene ..... Table 2. Repetition experiments on effect of pH on strontium adsorption. Polymer. Metal. Sr recovery. Sr recovery. Sr recovery concentration concentration.

  4. Sorption of Heavy Metal Ions from Mine Wastewater by Activated ...

    African Journals Online (AJOL)

    Michael

    2016-12-02

    Dec 2, 2016 ... Buah, W. K. and Dankwah, J. R. (2016), “Sorption of Heavy Metals from Mine Wastewater by Activated. Carbons Prepared ... A study on sorption of heavy metal ions: Lead (Pb2+), Copper (Cu2+) and Cadmium (Cd2+) from mine wastewater by activated ... (Pb), having relatively high densities and are toxic.

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

    African Journals Online (AJOL)

    GREGO

    2007-04-02

    Apr 2, 2007 ... diffusion rate constant, Ka show that adsorption of metal ions is particle diffusion controlled. The adsorbent produced from coconut fibre can be used to remove heavy metals from aqueous solution with high efficiency. Key words: Adsorption dynamics, fractional attianment of equilibrium, intraparticle ...

  6. [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.

  7. 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.

  8. Impact of metal ion homeostasis of genetically modified Escherichia coli Nissle 1917 and K12 (W3110) strains on colonization properties in the murine intestinal tract

    OpenAIRE

    Kupz, Andreas; Fischer, André; Nies, Dietrich H.; Grass, Gregor; Göbel, Ulf B.; Bereswill, Stefan; Heimesaat, Markus M.

    2013-01-01

    Metal ions are integral parts of pro- as well as eukaryotic cell homeostasis. Escherichia coli proved a valuable in vitro model organism to elucidate essential mechanisms involved in uptake, storage, and export of metal ions. Given that E. coli Nissle 1917 is able to overcome murine colonization resistance, we generated several E. coli Nissle 1917 mutants with defects in zinc, iron, copper, nickel, manganese homeostasis and performed a comprehensive survey of the impact of m...

  9. 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.

  10. High blood metal ion levels in 19 of 22 patients with metal-on-metal hinge knee replacements

    OpenAIRE

    Laitinen, Minna; Nieminen, Jyrki; Reito, Aleksi; Pakarinen, Toni-Karri; Suomalainen, Piia; Pamilo, Konsta; Parkkinen, Jyrki; Lont, Tonis; Eskelinen, Antti

    2017-01-01

    Background and purpose There has been increasing alarm regarding metal-on-metal (MoM) joint replacements leading to elevated levels of metal ions and adverse reactions to metal debris (ARMDs). There is little information available concerning the prevalence of and risk factors for these adverse reactions, except with MoM hip joint replacements. We determined the levels of metal ions in blood and the rate of revision due to ARMDs in patients treated with MoM hinge total knee arthroplasty (TKA)....

  11. Large fixed-size metal-on-metal total hip arthroplasty : higher serum metal ion levels in patients with pain

    NARCIS (Netherlands)

    Smeekes, Christiaan; Ongkiehong, Bastiaan; van der Wal, Bart; Wolterbeek, Ron; Henseler, Jan Ferdinand; Nelissen, Rob

    2015-01-01

    Purpose: Recently, concerns have arisen about metal-on-metal (MoM) total hip arthroplasty (THA). Therefore, the purpose of this cross-sectional cohort study was to describe the incidence of pain, pseudotumours, revisions and the relation between elevated metal ion levels, functional outcome and

  12. In vitro and in vivo metal ion release.

    Science.gov (United States)

    Brown, S A; Farnsworth, L J; Merritt, K; Crowe, T D

    1988-04-01

    A series of experiments was conducted to study in vitro and in vivo metal ion release and the urine excretion of metal ions. Metal salts were injected and urine analyzed. Anodic potentials were applied to stainless steel and cobalt-chromium-molybdenum (CCM) specimens to cause an acceleration of corrosion rates. Corrosion experiments were done in saline, 10% serum and in a subcutaneous space in hamsters. Corrosion rates were determined by measurements of weight loss and calculations of net charge transfer. Metal ion concentrations were determined with graphite furnace atomic absorption spectroscopy, and were calculated from total charge using Faraday's law. The results with stainless steel showed that the weight loss and metal ion release from stainless steel in vitro and in vivo can be calculated using Faraday's Law, assuming release in proportion to alloy composition. The results with CCM indicated that release rates in vitro can be used to determine the proportionality of release in vivo. All the nickel and most of the cobalt was rapidly excreted, while less than 50% of the chromium was excreted. The excretion of metals following salt injection or in vivo corrosion were very similar.

  13. Heavy metals in fish tissues/stomach contents in four marine wild commercially valuable fish species from the western continental shelf of South China Sea.

    Science.gov (United States)

    Gu, Yang-Guang; Lin, Qin; Huang, Hong-Hui; Wang, Liang-Gen; Ning, Jia-Jia; Du, Fei-Yan

    2017-01-30

    The concentrations of heavy metals (Cd, Pb, Cr, Ni, Cu and Zn) were determined in four commercially valuable fish species (Thunnus obesus, Decapterus lajang, Cubiceps squamiceps and Priacanthus macracanthus), collected in the western continental shelf of the South China Sea. Concentrations of Cd, Pb, Cr, Ni, Cu, and Zn in fish muscles were 0.006-0.050, 0.13-0.68, 0.18-0.85, 0.11-0.25, 0.12-0.77, and 2.41-4.73μg/g, wet weight, respectively. Concentrations of heavy metals in all species were below their acceptable daily upper limit, suggesting human consumption of these wild fish species may be safe, with health risk assessment based on the target hazard quotients (THQ) and total THQ, indicating no significant adverse health effects with consumption. The average concentrations of Zn were higher in gills than in stomach contents, backbones or muscle, while conversely, the other heavy metals had higher concentrations in stomach contents than in other tissues. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. Reducing hazardous heavy metal ions using mangium bark waste.

    Science.gov (United States)

    Khabibi, Jauhar; Syafii, Wasrin; Sari, Rita Kartika

    2016-08-01

    The objective of this study was to evaluate the characteristics of mangium bark and its biosorbent ability to reduce heavy metal ions in standard solutions and wastewater and to assess changes in bark characteristics after heavy metal absorption. The experiments were conducted to determine heavy metal absorption from solutions of heavy metals alone and in mixtures as well as from wastewater. The results show that mangium bark can absorb heavy metals. Absorption percentages and capacities from single heavy metal solutions showed that Cu(2+) > Ni(2+) > Pb(2+) > Hg(2+), while those from mixture solutions showed that Hg(2+) > Cu(2+) > Pb(2+) > Ni(2+). Wastewater from gold mining only contained Cu, with an absorption percentage and capacity of 42.87 % and 0.75 mg/g, respectively. The highest absorption percentage and capacity of 92.77 % and 5.18 mg/g, respectively, were found for Hg(2+) in a mixture solution and Cu(2+) in single-metal solution. The Cu(2+) absorption process in a single-metal solution changed the biosorbent characteristics of the mangium bark, yielding a decreased crystalline fraction; changed transmittance on hydroxyl, carboxyl, and carbonyl groups; and increased the presence of Cu. In conclusion, mangium bark biosorbent can reduce hazardous heavy metal ions in both standard solutions and wastewater.

  15. 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

  16. Formation of gels in the presence of metal ions.

    Science.gov (United States)

    Castellucci, Nicola; Falini, Giuseppe; Angelici, Gaetano; Tomasini, Claudia

    2011-08-01

    A small library of stereoisomeric pseudopeptides able to make gels in different solvents has been prepared and their attitude to make gels in the presence of several metal ions was evaluated. Four benzyl esters and four carboxylic acids, all containing a moiety of azelaic acid (a long chain dicarboxylic acid) coupled with four different pseudopeptide moieties sharing the same skeleton (a phenyl group one atom apart from the oxazolidin-2-one carboxylic group), were synthesized in solution, by standard coupling reaction. The tendency of these pseudopeptides to form gels was evaluated using the inversion test of 10 mM solutions of pure compounds and of stoichiometric mixtures of pseudopeptides and metal ions. To obtain additional information on the molecular association, the gel samples were left dry in the air to form xerogels that were further analyzed using SEM and XRD. The formation of gel containing Zn(II) or Cu(II) ions gave good results in term of incorporation of the metal ions, while the presence of Cu(I), Al(III) and Mg(II) gave less satisfactory results. This outcome is a first insight in the formation of stable LMWGs formed by stoichiometric mixtures of pseudopeptides and metal ions. Further studies will be carried out to develop similar compounds of pharmacological interest.

  17. 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.

  18. 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.

  19. Removal and recovery of toxic metal ions from aqueous waste sites using polymer pendant ligands

    Energy Technology Data Exchange (ETDEWEB)

    Fish, D. [Lawrence Berkeley National Lab., CA (United States)

    1996-10-01

    The purpose of this project is to investigate the use of polymer pendant ligand technology to remove and recover toxic metal ions from DOE aqueous waste sites. Polymer pendant lgiands are organic ligands, anchored to crosslinked, modified divinylbenzene-polystyrene beads, that can selectively complex metal ions. The metal ion removal step usually occurs through a complexation or ion exchange phenomena, thus recovery of the metal ions and reuse of the beads is readily accomplished.

  20. Nanopolysaccharides for adsorption of heavy metal ions from water

    OpenAIRE

    Liu, Peng

    2014-01-01

    With population expansion and industrialization, heavy metal has become one of the biggest and most toxic water pollutants, which is a serious problem for human society today. The aim of this work is to explore the potential of nanopolysaccharides including nanocellulose and nanochitin to remove metal ions from contaminated water. The above nano-polysaccharides are of interest in water purification technologies due to their high surface area, high mechanical properties, and versatile surface ...

  1. Heavy metal ions adsorption from mine waters by sawdust

    OpenAIRE

    G. Bogdanović; Milan Gorgievski; Dragana Božić; Velizar Stanković

    2009-01-01

    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 solut...

  2. 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.

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

    Science.gov (United States)

    Dauplais, Marc; Lazard, Myriam; Blanquet, Sylvain; Plateau, Pierre

    2013-01-01

    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.

  4. 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.

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

    African Journals Online (AJOL)

    NJD

    high stability.1,3,5 Porphyrin reagents have therefore received increasing attention and are widely applied for the simulta- neous determination of metal ions.9–19. The determination of trace amounts of lead, cadmium, mercury, nickel, cobalt and tin in tobacco and tobacco additives is important because of the biological ...

  6. Dislocation loop formation by swift heavy ion irradiation of metals

    Science.gov (United States)

    Khara, Galvin S.; Murphy, Samuel T.; Duffy, Dorothy M.

    2017-07-01

    A coupled two-temperature, molecular dynamics methodology is used to simulate the structural evolution of bcc metals (Fe and W) and fcc metals (Cu and Ni) following irradiation by swift heavy ions. Electronic temperature dependent electronic specific heat capacities and electron-phonon coupling strengths are used to capture the full effects of the variation in the electronic density of states. Tungsten is found to be significantly more resistant to damage than iron, due both to the higher melting temperature and the higher thermal conductivity. Very interesting defect structures, quite different from defects formed in cascades, are found to be created by swift heavy ion irradiation in the bcc metals. Isolated vacancies form a halo around elongated interstitial dislocation loops that are oriented along the ion path. Such configurations are formed by rapid recrystallization of the molten cylindrical region that is created by the energetic ion. Vacancies are created at the recrystallization front, resulting in excess atoms at the core which form interstitial dislocation loops on completion of crystallization. These unique defect structures could, potentially, be used to create metal films with superior mechanical properties and interesting nanostructures.

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

    Indian Academy of Sciences (India)

    tural and chemical properties of the composites were studied by means of an LCR meter, X-ray diffraction, FTIR spectroscopy and SEM/AFM, ... This reveals that ion beam irradiation promotes the metal/polymer bonding and converts polymeric ... stirrer at a high speed of around 700 rpm until all polymer grains dissolved.

  8. 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 ...

  9. Conformations and vibrational spectroscopy of metal-ion/polylalanine complexes

    NARCIS (Netherlands)

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

    2010-01-01

    The thermochemistry and structures of complexes of dialanine and trialanine with a series of singly and doubly charged metal ions have been examined by spectroscopic and computational approaches. Complexes with Li+, K+, Cs+, Ca2+, Sr2+ and Ba2+ were formed by electrospray ionization, and studied by

  10. 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 ...

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

    African Journals Online (AJOL)

    NICO

    A recent technique involving the use of paper electrophoresis is described for the study of equilibria in binary complex systems in solution. The stability ... metal ions have several significant applications in biological systems.3–20 Beryllium is ... complexes and no reports on Be(II)-hydroxyproline binary complexes. In view of ...

  12. 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 ...

  13. 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....

  14. Liquid metal ion source and alloy for ion emission of multiple ionic species

    Science.gov (United States)

    Clark, Jr., William M.; Utlaut, Mark W.; Wysocki, Joseph A.; Storms, Edmund K.; Szklarz, Eugene G.; Behrens, Robert G.; Swanson, Lynwood W.; Bell, Anthony E.

    1987-06-02

    A liquid metal ion source and alloy for the simultaneous ion evaporation of arsenic and boron, arsenic and phosphorus, or arsenic, boron and phosphorus. The ionic species to be evaporated are contained in palladium-arsenic-boron and palladium-arsenic-boron-phosphorus alloys. The ion source, including an emitter means such as a needle emitter and a source means such as U-shaped heater element, is preferably constructed of rhenium and tungsten, both of which are readily fabricated. The ion sources emit continuous beams of ions having sufficiently high currents of the desired species to be useful in ion implantation of semiconductor wafers for preparing integrated circuit devices. The sources are stable in operation, experience little corrosion during operation, and have long operating lifetimes.

  15. 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.

  16. Molecular design of the microbial cell surface toward the recovery of metal ions.

    Science.gov (United States)

    Kuroda, Kouichi; Ueda, Mitsuyoshi

    2011-06-01

    The genetic engineering of microorganisms to adsorb metal ions is an attractive method to facilitate the environmental cleanup of metal pollution and to enrich the recovery of metal ions such as rare metal ions. For the recovery of metal ions by microorganisms, cell surface design is an effective strategy for the molecular breeding of bioadsorbents as an alternative to intracellular accumulation. The cell surface display of known metal-binding proteins/peptides and the molecular design of novel metal-binding proteins/peptides have been performed using a cell surface engineering approach. The adsorption of specific metal ions is the important challenge for the practical recovery of metal ions. In this paper, we discuss the recent progress in surface-engineered bioadsorbents for the recovery of metal ions. Copyright © 2011 Elsevier Ltd. All rights reserved.

  17. Chitosan removes toxic heavy metal ions from cigarette mainstream smoke

    Science.gov (United States)

    Zhou, Wen; Xu, Ying; Wang, Dongfeng; Zhou, Shilu

    2013-09-01

    This study investigated the removal of heavy metal ions from cigarette mainstream smoke using chitosan. Chitosan of various deacetylation degrees and molecular weights were manually added to cigarette filters in different dosages. The mainstream smoke particulate matter was collected by a Cambridge filter pad, digested by a microwave digestor, and then analyzed for contents of heavy metal ions, including As(III/V), Pb(II), Cd(II), Cr(III/VI) and Ni(II), by graphite furnace atomic absorption spectrometry (GFAAS). The results showed that chitosan had a removal effect on Pb(II), Cd(II), Cr(III/VI) and Ni(II). Of these, the percent removal of Ni(II) was elevated with an increasing dosage of chitosan. Chitosan of a high deace tylation degree exhibited good binding performance toward Cd(II), Cr(III/VI) and Ni(II), though with poor efficiency for Pb(II). Except As(III/V), all the tested metal ions showed similar tendencies in the growing contents with an increasing chitosan molecular weight. Nonetheless, the percent removal of Cr(III/VI) peaked with a chitosan molecular weight of 200 kDa, followed by a dramatic decrease with an increasing chitosan molecular weight. Generally, chitosan had different removal effects on four out of five tested metal ions, and the percent removal of Cd(II), Pb(II), Cr(III/VI) and Ni(II) was approximately 55%, 45%, 50%, and 16%, respectively. In a word, chitosan used in cigarette filter can remove toxic heavy metal ions in the mainstream smoke, improve cigarette safety, and reduce the harm to smokers.

  18. Metal ion influence on eumelanin fluorescence and structure

    Science.gov (United States)

    Sutter, Jens-Uwe; Birch, David J. S.

    2014-06-01

    Melanin has long been thought to have an unworkably weak and complex fluorescence, but here we study its intrinsic fluorescence in order to demonstrate how metal ions can be used to control the rate of formation, constituents and structure of eumelanin formed from the well-known laboratory auto-oxidation of 3,4-dihydroxy-L-phenylalanine (L-DOPA). The effect on eumelanin absorption and fluorescence of a range of solvated metal ions is reported including Cu, Zn, Ni, Na and K. Monovalent cations and Zn have little effect, but the effect of transition metal cations can be considerable. For example, at pH 10, copper ions are shown to accelerate the onset of eumelanin formation, but not the rate of formation once it commences, and simplify the usual complex structure and intrinsic fluorescence of eumelanin in a way that is consistent with an increased abundance of 5,5-dihydroxyindole-2-carboxylic acid (DHICA). The presence of a dominant 6 ns fluorescence decay time at 480 nm, when excited at 450 nm describes a distinct photophysical species, which we tentatively assign to small oligomers. Copper is well-known to normally quench fluorescence, but increasing amounts of copper surprisingly leads to an increase in the fluorescence decay time of eumelanin, while reducing the fluorescence intensity, suggesting copper modification of the excited state. Such results have bearing on diverse areas. The most accepted morphology for melanin is that of a graphite-like sheet structure, and one which readily binds metal ions, an interaction that is thought to have an important, though as yet unclear bearing on several areas of medicine including neurology. There is also increasing interest in bio-mimicry by preparing and labelling sheet structures with metal ions for new electronic and photonic materials.

  19. 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.

  20. 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.

  1. 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...

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

    Energy Technology Data Exchange (ETDEWEB)

    Bischoff, Lothar, E-mail: l.bischoff@hzdr.de [Helmholtz-Zentrum Dresden-Rossendorf, Institute of Ion Beam Physics and Materials Research, Bautzner Landstrasse 400, 01328 Dresden (Germany); Mazarov, Paul, E-mail: Paul.Mazarov@raith.de; Bruchhaus, Lars, E-mail: Lars.Bruchhaus@raith.de [Raith GmbH, Konrad-Adenauer-Allee 8, 44263 Dortmund (Germany); Gierak, Jacques, E-mail: jacques.gierak@lpn.cnrs.fr [LPN-CNRS, Route de Nozay, 91460 Marcoussis (France)

    2016-06-15

    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.

  3. Mechanical property measurements on ion-irradiated metals

    Energy Technology Data Exchange (ETDEWEB)

    Zinkle, S.J.; Oliver, W.C.

    1986-08-01

    A recently developed mechanical properties microprobe (MPM) has been used to investigate strength and elastic modulus changes in ion-irradiated metals. The indenter load and its displacement are simultaneously monitored while the indentation is being made and also during unloading. Microindentation hardness measurements have been performed on ion-irradiated copper and Cu-0.15% Zr (AMZIRC). The depth dependence of the ion damage has been investigated in selected specimens which were prepared using a cross-section technique. This procedure allows a direct comparison to be made of hardness data from different irradiation depths while the indent size is held constant. The displacement damage associated with ion irradiation caused either hardening or softening, depending on the irradiation conditions and the material.

  4. 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.

  5. Metal-on-metal bearings total hip arthroplasty: the cobalt and chromium ions release concern.

    Science.gov (United States)

    Delaunay, C; Petit, I; Learmonth, I D; Oger, P; Vendittoli, P A

    2010-12-01

    With certain concerns recently reported on metal-on-metal bearing couples in total hip arthroplasty, this study's objective is to review the current knowledge concerning release of metal ions and its potential consequences. Each metal-on-metal implant presents different tribological properties. The analytical techniques for metals are accurate and the Co ion rates seem acceptable up to 2 μg/L. A delayed type IV hypersensitivity reaction (atypical lymphocytic vasculitis-associated lesion [ALVAL]) may be the source of arthroplasty failure. Idiosyncratic, it remains unpredictable even using cutaneous tests and apparently is rare (0.3%). Today, there are no scientific or epidemiologic data supporting a risk of carcinogenesis or teratogenesis related to the use of a metal-on-metal bearings couple. Solid pseudotumors nearly exclusively are observed with resurfacing procedures, carrying a high annual revision rate in women under 40 years of age, occurring particularly in cases of acetabular malposition and with use of cast molded Cr-Co alloys. Osteolysis manifests through complete and progressive radiolucent lines or through cavitary lesions stemming from ALVAL-type alterations or impingement problems or implant incompatibility. The formation of wear debris exceeding the biological tolerance is possible with implant malposition, subluxation, and jamming of the femoral head in cases of cup deformity. Moreover, each implant presents different metal ion production; assessment of their performance and safety is required before their clinical use. With the knowledge available today, metal-on-metal bearing couples are contraindicated in cases of metal allergies or end stage renal dysfunction and small size resurfacing should cautiously be used. Copyright © 2010. Published by Elsevier Masson SAS.

  6. Transition metal ions: charge carriers that mediate the electron capture dissociation pathways of peptides.

    Science.gov (United States)

    Chen, Xiangfeng; Fung, Yi Man Eva; Chan, Wai Yi Kelly; Wong, Pui Shuen; Yeung, Hoi Sze; Chan, T-W Dominic

    2011-12-01

    Electron capture dissociation (ECD) of model peptides adducted with first row divalent transition metal ions, including Mn(2+), Fe(2+), Co(2+), Ni(2+), Cu(2+), and Zn(2+), were investigated. Model peptides with general sequence of ZGGGXGGGZ were used as probes to unveil the ECD mechanism of metalated peptides, where X is either V or W; and Z is either R or N. Peptides metalated with different divalent transition metal ions were found to generate different ECD tandem mass spectra. ECD spectra of peptides metalated by Mn(2+) and Zn(2+) were similar to those generated by ECD of peptides adducted with alkaline earth metal ions. Series of c-/z-type fragment ions with and without metal ions were observed. ECD of Fe(2+), Co(2+), and Ni(2+) adducted peptides yielded abundant metalated a-/y-type fragment ions; whereas ECD of Cu(2+) adducted peptides generated predominantly metalated b-/y-type fragment ions. From the present experimental results, it was postulated that electronic configuration of metal ions is an important factor in determining the ECD behavior of the metalated peptides. Due presumably to the stability of the electronic configuration, metal ions with fully-filled (i.e., Zn(2+)) and half filled (i.e., Mn(2+)) d-orbitals might not capture the incoming electron. Dissociation of the metal ions adducted peptides would proceed through the usual ECD channel(s) via "hot-hydrogen" or "superbase" intermediates, to form series of c-/z(•)- fragments. For other transition metal ions studied, reduction of the metal ions might occur preferentially. The energy liberated by the metal ion reduction would provide enough internal energy to generate the "slow-heating" type of fragment ions, i.e., metalated a-/y- fragments and metalated b-/y- fragments. © American Society for Mass Spectrometry, 2011

  7. Polymer Catalysts Imprinted with Metal Ions as Biomimics of Metalloenzymes

    Directory of Open Access Journals (Sweden)

    Joanna Czulak

    2013-01-01

    Full Text Available This work presents the preparation and properties of molecularly imprinted polymers (MIPs with catalytic centers that mimic the active sites of metalloenzymes. The MIP synthesis was based on suspension polymerization of functional monomers (4-vinylpyridine and acrylonitrile with trimethylolpropane trimethacrylate as a crosslinker in the presence of transition metal ions and 4-methoxybenzyl alcohol as a template. Four metal ions have been chosen for imprinting from among the microelements that are the most essential in the native enzymes: Cu2+, Co2+, Mn2+, and Zn2+. To prepare catalysts, the required loading of metal ions was obtained during sorption process. The catalysts imprinted with Cu2+, Co2+, and Zn2+ were successfully used for hydroquinone oxidation in the presence of hydrogen peroxide. The Mn2+-imprinted catalyst showed no activity due to the insufficient metal loading. Cu2+ MIP showed the highest efficiency. In case of Cu- and Co-MIP catalysts, their activity was additionally increased by the use of surface imprinting technique.

  8. 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.

  9. Conversion of agonist site to metal-ion chelator site in the beta(2)-adrenergic receptor

    DEFF Research Database (Denmark)

    Elling, C E; Thirstrup, K; Holst, Birgitte

    1999-01-01

    effect of, for example Cu(2+), and in several cases increased the affinity of the ions for the agonistic site. Wash-out experiments and structure-activity analysis indicated, that the high-affinity chelators and the metal ions bind and activate the mutant receptor as metal ion guided ligand complexes...... in the mutant receptors not by normal catecholamine ligands but instead either by free zinc ions or by zinc or copper ions in complex with small hydrophobic metal-ion chelators. Chelation of the metal ions by small hydrophobic chelators such as phenanthroline or bipyridine protected the cells from the toxic....... Because of the well-understood binding geometry of the small metal ions, an important distance constraint has here been imposed between TM-III and -VII in the active, signaling conformation of 7TM receptors. It is suggested that atoxic metal-ion chelator complexes could possibly in the future be used...

  10. 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 ...

  11. 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.

  12. Photoelectric properties in metal ion modified DNA nanostructure.

    Science.gov (United States)

    Kulkarni, Atul; Dugasani, Sreekantha Reddy; Jang Ah Kim; Kim; Sung Ha Park; Taesung Kim

    2015-08-01

    Due to specific or as designed self-assembly, DNA nanostructures gaining popularity in various nanoscale electronic applications. Herein, a novel divalent metal ion-DNA complex known as M-DNA have been investigated for its photoelectric characteristics. The increased conductivity of M-DNA thin films is attributed to the metal ion electrical and optical properties. The gate voltage effect along with illumination on the conductivity of M-DNA demonstrates that M-DNA can be used as an active element of a field-effect transistor. The Zn DNA shows maximum conductivity of 300μS/cm at 480 nm light illumination suggest that M-DNA can be utilized in nano-opto-electronics and bio-sensing applications.

  13. 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.

  14. Speciation of heavy metal ions as influenced by interactions with montmorillonite, Al hydroxide polymers and citrate

    NARCIS (Netherlands)

    Janssen, R.P.T.

    1995-01-01

    Clay minerals, metal-hydroxides and organic matter can bind metal ions; moreover they also interact with each other. These mutual interactions influence the metal binding to a significant extent. In this study, the speciation of the heavy metal ions Zn and Ph was investigated in model

  15. Spent lithium-ion battery recycling - Reductive ammonia leaching of metals from cathode scrap by sodium sulphite.

    Science.gov (United States)

    Zheng, Xiaohong; Gao, Wenfang; Zhang, Xihua; He, Mingming; Lin, Xiao; Cao, Hongbin; Zhang, Yi; Sun, Zhi

    2017-02-01

    Recycling of spent lithium-ion batteries has attracted wide attention because of their high content of valuable and hazardous metals. One of the difficulties for effective metal recovery is the separation of different metals from the solution after leaching. In this research, a full hydrometallurgical process is developed to selectively recover valuable metals (Ni, Co and Li) from cathode scrap of spent lithium ion batteries. By introducing ammonia-ammonium sulphate as the leaching solution and sodium sulphite as the reductant, the total selectivity of Ni, Co and Li in the first-step leaching solution is more than 98.6% while it for Mn is only 1.36%. In detail understanding of the selective leaching process is carried out by investigating the effects of parameters such as leaching reagent composition, leaching time (0-480min), agitation speed (200-700rpm), pulp density (10-50g/L) and temperature (323-353K). It was found that Mn is primarily reduced from Mn4+ into Mn2+ into the solution as [Formula: see text] while it subsequently precipitates out into the residue in the form of (NH4)2Mn(SO3)2·H2O. Ni, Co and Li are leached and remain in the solution either as metallic ion or amine complexes. The optimised leaching conditions can be further obtained and the leaching kinetics is found to be chemical reaction control under current leaching conditions. As a result, this research is potentially beneficial for further optimisation of the spent lithium ion battery recycling process after incorporating with metal extraction from the leaching solution. Copyright © 2016 Elsevier Ltd. All rights reserved.

  16. Chemical modification of Chitosan for metal ion removal

    Directory of Open Access Journals (Sweden)

    Tariq R.A. Sobahi

    2014-11-01

    Full Text Available In the current work some modification reactions have been conducted to modify Chitosan with some organic compounds, such as aldehydes and organic acids. On the other hand, different blends of Chitosan with some carbohydrates were prepared to obtain Chitosan derivatives of certain physical and chemical properties. The obtained products have been characterized with the necessary chemical and spectroscopic techniques. The efficiency of the obtained modified materials has been investigated for separation of metal ions and for water uptake.

  17. 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.

  18. Nanostructure operations by means of the liquid metal ion sources.

    Science.gov (United States)

    Gasanov, I S; Gurbanov, I I

    2012-02-01

    Characteristics of a disperse phase of liquid metal ion source on the basis of various working substances are investigated. It is revealed that generation of the charged particles occurs in the threshold image and is simultaneously accompanied by excitation of capillary instability on a surface of the emitter. The majority of particles has the size about 2 nm (Sn) and a specific charge of 5 × 10(4) C∕kg. If the working liquid possesses high viscosity (Ni), generation of nanodroplets does not occur. Gold nanoparticles are used for deposition on a surface of quartz cantilevers with the purpose of increase in sensitivity of biosensors and on an external surface of carbon nanotubes for creation pressure sensors. By means of an ion source nanostructures can be etched on a flat surface of conductive materials without difficult ion optics.

  19. Seasonal changes in chemical and mineralogical composition of sewage sludge incineration residues and their potential for metallic elements and valuable components recovery

    Science.gov (United States)

    Kasina, Monika; Kowalski, Piotr R.; Michalik, Marek

    2017-04-01

    collected in the spring 2016. The highest concentrations for most of the elements were measured in summer 2016 except for the Ca, Sn, Zn, Cd, Sb, and Ag which concentrations were the highest in the winter time 2015. Even though the seasonal changes in metallic and/or potentially valuable elements concentrations are visible their overall content is low. In addition they are dispersed within crystalline and amorphous phase, therefore it seems to be inappropriate to consider this material as a source of valuable elements. Due to high phosphorus content in the fly ash, equal to the low grade phosphorus ore, both in the form of phosphate minerals as well as dispersed within minerals can be treated as a potential source of this critical raw material. Acknowledgment: The study was supported by Polish National Science Centre. NCN grant No UMO-2014/15/B/ST10/04171

  20. Adsorption of heavy metal ions by immobilized phytic acid

    Energy Technology Data Exchange (ETDEWEB)

    Tsao, G.T.; Zheng, Yizhou; Lu, J.; Gong, Cheng S. [Purdue Univ., West Lafayette, IN (United States)

    1997-12-31

    Phytic acid (myoinositol hexaphosphate) or its calcium salt, phytate, is an important plant constituents. It accounts for up to 85% of total phosphorus in cereals and legumes. Phytic acid has 12 replaceable protons in the phytic molecule rendering it the ability to complex with multivalent cations and positively charged proteins. Poly 4-vinyl pyridine (PVP) and other strong-based resins have the ability to adsorb phytic acid. PVP has the highest adsorption capacity of 0.51 phytic acid/resins. The PVP resin was used as the support material for the immobilization of phytic acid. The immobilized phytic acid can adsorb heavy metal ions, such as cadmium, copper, lead, nickel, and zinc ions, from aqueous solutions. Adsorption isotherms of the selected ions by immobilized phytic acid were conducted in packed-bed column at room temperature. Results from the adsorption tests showed 6.6 mg of Cd{sup 2+}, 7 mg of Cu{sup 2+}, 7.2 mg of Ni{sup 2+}, 7.4 mg of Pb{sup 2+}, and 7.7 mg of Zn{sup 2+} can be adsorbed by each gram of PVP-phytic acid complex. The use of immobilized phytic acid has the potential for removing metal ions from industrial or mining waste water. 15 refs., 7 figs., 2 tabs.

  1. Catalytic potential of selected metal ions for bioleaching, and potential techno-economic and environmental issues: A critical review.

    Science.gov (United States)

    Pathak, Ashish; Morrison, Liam; Healy, Mark Gerard

    2017-04-01

    Bioleaching is considered to be a low-cost, eco-friendly technique for leaching valuable metals from a variety of matrixes. However, the inherent slow dissolution kinetics and low metal leaching yields have restricted its wider commercial applicability. Recent advancements in bio-hydrometallurgy have suggested that these critical issues can be successfully alleviated through the addition of a catalyst. The catalyzing properties of a variety of metals ions (Ag + , Hg ++ , Bi +++ , Cu ++ , Co ++ etc.) during bioleaching have been successfully demonstrated. In this article, the role and mechanisms of these metal species in catalyzing bioleaching from different minerals (chalcopyrite, complex sulfides, etc.) and waste materials (spent batteries) are reviewed, techno-economic and environmental challenges associated with the use of metals ions as catalysts are identified, and future prospectives are discussed. Based on the analysis, it is suggested that metal ion-catalyzed bioleaching will play a key role in the development of future industrial bio-hydrometallurgical processes. Copyright © 2017 Elsevier Ltd. All rights reserved.

  2. 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

  3. Phytoremediation: an overview of metallic ion decontamination from soil

    Energy Technology Data Exchange (ETDEWEB)

    Singh, O.V.; Labana, S.; Pandey, G.; Budhiraja, R.; Jain, R.K. [Inst. of Microbial Technology, Chandigarh (India)

    2003-07-01

    In recent years, phytoremediation has emerged as a promising ecoremediation technology, particularly for soil and water cleanup of large volumes of contaminated sites. The exploitation of plants to remediate soils contaminated with trace elements could provide a cheap and sustainable technology for bioremediation. Many modern tools and analytical devices have provided insight into the selection and optimization of the remediation process by plant species. This review describes certain factors for the phytoremediation of metal ion decontamination and various aspects of plant metabolism during metallic decontamination. Metal-hyperaccumulating plants, desirable for heavily polluted environments, can be developed by the introduction of novel traits into high biomass plants in a transgenic approach, which is a promising strategy for the development of effective phytoremediation technology. The genetic manipulation of a phytoremediator plant needs a number of optimization processes, including mobilization of trace elements/metal ions, their uptake into the root, stem and other viable parts of the plant and their detoxification and allocation within the plant. This upcoming science is expanding as technology continues to offer new, low-cost remediation options. (orig.)

  4. 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......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...

  5. 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

  6. Luminescent zinc metal-organic framework (ZIF-90) for sensing metal ions, anions and small molecules.

    Science.gov (United States)

    Liu, Chang; Yan, Bing

    2015-09-26

    We synthesize a zinc zeolite-type metal-organic framework, the zeolitic imidazolate framework (ZIF-90), which exhibits an intense blue luminescence excited under visible light. Luminescent studies indicate that ZIF-90 could be an efficient multifunctional fluorescence material for high sensitivity metal ions, anions and organic small molecules, especially for Cd(2+), Cu(2+), CrO4(2-) and acetone. The luminescence intensity of ZIF-90 increases with the concentration of Cd(2+) and decreases proportionally with the concentration of Cu(2+), while the same quenched experimental phenomena appear in the sensing of CrO4(2-). With the increase of the amount of acetone, the luminescence intensity decreases gradually in the emulsions of ZIF-90. The mechanism of the sensing properties is studied in detail as well. This study shows that ZIF-90 could be a useful luminescent sensor for metal ions, anions and organic small molecules.

  7. Portable Multispectral Colorimeter for Metallic Ion Detection and Classification

    Science.gov (United States)

    Jaimes, Ruth F. V. V.; Borysow, Walter; Gomes, Osmar F.; Salcedo, Walter J.

    2017-01-01

    This work deals with a portable device system applied to detect and classify different metallic ions as proposed and developed, aiming its application for hydrological monitoring systems such as rivers, lakes and groundwater. Considering the system features, a portable colorimetric system was developed by using a multispectral optoelectronic sensor. All the technology of quantification and classification of metallic ions using optoelectronic multispectral sensors was fully integrated in the embedded hardware FPGA ( Field Programmable Gate Array) technology and software based on virtual instrumentation (NI LabView®). The system draws on an indicative colorimeter by using the chromogen reagent of 1-(2-pyridylazo)-2-naphthol (PAN). The results obtained with the signal processing and pattern analysis using the method of the linear discriminant analysis, allows excellent results during detection and classification of Pb(II), Cd(II), Zn(II), Cu(II), Fe(III) and Ni(II) ions, with almost the same level of performance as for those obtained from the Ultravioled and visible (UV-VIS) spectrophotometers of high spectral resolution. PMID:28788082

  8. Portable Multispectral Colorimeter for Metallic Ion Detection and Classification

    Directory of Open Access Journals (Sweden)

    Mauro S. Braga

    2017-07-01

    Full Text Available This work deals with a portable device system applied to detect and classify different metallic ions as proposed and developed, aiming its application for hydrological monitoring systems such as rivers, lakes and groundwater. Considering the system features, a portable colorimetric system was developed by using a multispectral optoelectronic sensor. All the technology of quantification and classification of metallic ions using optoelectronic multispectral sensors was fully integrated in the embedded hardware FPGA ( Field Programmable Gate Array technology and software based on virtual instrumentation (NI LabView®. The system draws on an indicative colorimeter by using the chromogen reagent of 1-(2-pyridylazo-2-naphthol (PAN. The results obtained with the signal processing and pattern analysis using the method of the linear discriminant analysis, allows excellent results during detection and classification of Pb(II, Cd(II, Zn(II, Cu(II, Fe(III and Ni(II ions, with almost the same level of performance as for those obtained from the Ultravioled and visible (UV-VIS spectrophotometers of high spectral resolution.

  9. 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)

  10. 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.

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

    Science.gov (United States)

    Ke, Fu-Sheng; Wu, Yu-Shan; Deng, Hexiang

    2015-03-01

    Porous materials have been widely used in batteries and supercapacitors attribute to their large internal surface area (usually 100-1000 m2 g-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 m2 g-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.

  12. Retention of metal and sulphate ions from acidic mining water by anionic nanofibrillated cellulose.

    Science.gov (United States)

    Venäläinen, Salla H; Hartikainen, Helinä

    2017-12-01

    We carried out an adsorption experiment to investigate the ability of anionic nanofibrillated cellulose (NFC) to retain metal and SO42- ions from authentic highly acidic (pH3.2) mining water. Anionic NFC gels of different consistencies (1.1-%, 1.4-% and 1.8-% w/w) were allowed to react for 10min with mining water, after which NFC-induced changes in the metal and SO42- concentrations of the mining water were determined. The sorption capacities of the NFC gels were calculated as the difference between the element concentrations in the untreated and NFC-treated mining water samples. All the NFCs efficiently co-adsorbed both metals and SO42-. The retention of metals was concluded to take place through formation of metal-ligand complexes. The reaction between the NFC ligand and the polyvalent cations renders the cellulose nanofibrils positively charged and, thus, able to retain SO42- electrostatically. Adsorption capacity of the NFC gels substantially increased upon decreasing DM content as a result of the dilution-induced weakening of the mutual interactions between individual cellulose nanofibrils. This outcome reveals that the dilution of the NFC gel not only increases its purification capacity but also reduces the demand for cellulosic raw material. These results suggest that anionic NFC made of renewable materials serves as an environmentally sound and multifunctional purification agent for acidic multimetal mining waters or AMDs of high ionic strength. Unlike industrial minerals traditionally used to precipitate valuable metals from acidic mining effluents before their permanent disposal from the material cycle, NFC neither requires mining of unrenewable raw materials nor produces inorganic sludges. Copyright © 2017 Elsevier B.V. All rights reserved.

  13. Electrolyte materials containing highly dissociated metal ion salts

    Energy Technology Data Exchange (ETDEWEB)

    Lee, H.S.; Geng, L.; Skotheim, T.A.

    1996-07-23

    The present invention relates to metal ion salts which can be used in electrolytes for producing electrochemical devices, including both primary and secondary batteries, photoelectrochemical cells and electrochromic displays. The salts have a low energy of dissociation and may be dissolved in a suitable polymer to produce a polymer solid electrolyte or in a polar aprotic liquid solvent to produce a liquid electrolyte. The anion of the salts may be covalently attached to polymer backbones to produce polymer solid electrolytes with exclusive cation conductivity. 2 figs.

  14. Electrolyte materials containing highly dissociated metal ion salts

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Hung-Sui (East Setauket, NY); Geng, Lin (Coram, NY); Skotheim, Terje A. (Shoreham, NY)

    1996-07-23

    The present invention relates to metal ion salts which can be used in electrolytes for producing electrochemical devices, including both primary and secondary batteries, photoelectrochemical cells and electrochromic displays. The salts have a low energy of dissociation and may be dissolved in a suitable polymer to produce a polymer solid electrolyte or in a polar aprotic liquid solvent to produce a liquid electrolyte. The anion of the salts may be covalently attached to polymer backbones to produce polymer solid electrolytes with exclusive cation conductivity.

  15. Clusters distributions on charges and dimensions at ion metal sputtering

    CERN Document Server

    Matveev, V I

    2001-01-01

    The theory on the metal sputtering in form of large (with the atoms number N >= 5) neutral and charged clusters under the impact of the ion bombardment is considered. The probability of the cluster emission, consisting of the N atoms, is calculated on the basis of the Einstein model. The charge state of the cluster, consisting of the N atoms, is determined. The obtained formulae agree well with the experimental results. It is noted, that the mass-spectra of the neutral clusters slightly depend on the target temperature, whereas the mass-spectra of the single charge clusters essentially depend on the target temperature

  16. 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.

  17. 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....

  18. Structure of the alkali-metal-atom + strontium molecular ions: Towards photoassociation and formation of cold molecular ions

    Energy Technology Data Exchange (ETDEWEB)

    Aymar, M.; Dulieu, O. [Laboratoire Aime Cotton, CNRS, UPR3321, Ba circumflex t. 505, Univ Paris-Sud, 91405 Orsay Cedex (France); Guerout, R. [Laboratoire Kastler-Brossel, CNRS, ENS, Univ Pierre et Marie Curie case 74, Campus Jussieu, F-75252 Paris Cedex 05 (France)

    2011-08-14

    The potential energy curves, permanent and transition dipole moments, and the static dipolar polarizability, of molecular ions composed of one alkali-metal atom and a strontium ion are determined with a quantum chemistry approach. The molecular ions are treated as effective two-electron systems and are treated using effective core potentials including core polarization, large gaussian basis sets, and full configuration interaction. In the perspective of upcoming experiments aiming at merging cold atom and cold ion traps, possible paths for radiative charge exchange, photoassociation of a cold lithium or rubidium atom and a strontium ion are discussed, as well as the formation of stable molecular ions.

  19. 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

  20. High blood metal ion levels in 19 of 22 patients with metal-on-metal hinge knee replacements.

    Science.gov (United States)

    Laitinen, Minna; Nieminen, Jyrki; Reito, Aleksi; Pakarinen, Toni-Karri; Suomalainen, Piia; Pamilo, Konsta; Parkkinen, Jyrki; Lont, Tonis; Eskelinen, Antti

    2017-06-01

    Background and purpose - There has been increasing alarm regarding metal-on-metal (MoM) joint replacements leading to elevated levels of metal ions and adverse reactions to metal debris (ARMDs). There is little information available concerning the prevalence of and risk factors for these adverse reactions, except with MoM hip joint replacements. We determined the levels of metal ions in blood and the rate of revision due to ARMDs in patients treated with MoM hinge total knee arthroplasty (TKA). Patients and methods - 22 patients with TKAs and MoM hinge connecting mechanisms were studied for whole-blood chromium and cobalt levels at 6 months, 1 year, and/or ≥2 years after surgery. Possible ARMDs were investigated by MRI. 12 patients with TKAs and metal-on-polyethylene (MoP) connecting mechanisms served as controls. Results - The cobalt levels were over 5 ppb in 19 of the 22 patients in the MoM group and in 1 of the 12 patients in the MoP group. The chromium levels were over 5 ppb in 11 of the 22 patients in the MoM group and in none of the 12 patients in the MoP group. Pseudotumors were operated in 4 of the 22 patients in the MoM group and in none of the patients in the MoP group. Interpretation - Our results clearly show that the MoM hinge TKA carries a high risk of increased levels of systemic metal ions and also local ARMD, leading to complicated knee revisions. We therefore discourage the use of MoM hinge TKA.

  1. Specificity of the metalloregulator CueR for monovalent metal ions

    DEFF Research Database (Denmark)

    Szunyogh, Dániel; Szokolai, Hajnalka; Thulstrup, Peter Waaben

    2015-01-01

    Metal-ion-responsive transcriptional regulators within the MerR family effectively discriminate between mono- and divalent metal ions. Herein we address the origin of the specificity of the CueR protein for monovalent metal ions. Several spectroscopic techniques were employed to study Ag(I) , Zn...... members of the MerR family is proposed. For CueR, the mechanism relies on the protonation of Cys 112....

  2. Mutual separation of metal ions by dithizone extraction-isotachophoresis on the basis of HSAB principle

    Energy Technology Data Exchange (ETDEWEB)

    Kawamoto, Hiroshi; Itabashi, Hideyuki; Ohnuki, Tomoyuki (Gunma Univ., Kiryu (Japan). Faculty of Engineering)

    1994-09-01

    Based on the hard and soft acids and bases (HSAB) principle, a method for extraction of metal ions with dithizone was developed for preconcentration and separation of trace metal ions. The extracted metal ions in organic phase were back-extracted to EDTA solution. The resulting solution was applied to isotachophoretic analysis. The separation of zinc(II), cadmium(II) and lead(II) at the 10[sup -6] mol dm[sup -3] level could performed by the present method. (author).

  3. Electrochemical Investigation of Anthraquinone-Based Chemodosimeter for Cu2+ Metal Ion

    Directory of Open Access Journals (Sweden)

    Yeo Woon Yoon

    2013-01-01

    Full Text Available The electrochemical properties of an anthraquinone-containing Cu2+-promoted desulfurization chemodosimeter (AQCD in the presence of various metal ions were investigated by voltammetry. AQCD showed voltammetric changes toward divalent metal ions (M2+, which are similar to those of anthraquinone (AQ and 1-aminoanthraquinone (AQNH2 with the metal ions except Cu2+. This can be explained on the electrostatic interaction (AQCD-M2+ and chemodosimetric reaction (AQCD-Cu2+.

  4. MINAS-a database of Metal Ions in Nucleic AcidS

    OpenAIRE

    Joachim Schnabl; Pascal Suter; Roland K. O. Sigel

    2012-01-01

    Correctly folded into the respective native 3D structure, RNA and DNA are responsible for uncountable key functions in any viable organism. In order to exert their function, metal ion cofactors are closely involved in folding, structure formation and, e.g. in ribozymes, also the catalytic mechanism. The database MINAS, Metal Ions in Nucleic AcidS (http://www.minas.uzh.ch), compiles the detailed information on innersphere, outersphere and larger coordination environment of > 70 000 metal ions ...

  5. Adsorption of heavy metal ion from aqueous single metal solution by chemically modified sugarcane bagasse.

    OpenAIRE

    Karnitz Júnior, Osvaldo; Gurgel, Leandro Vinicius Alves; Melo, Júlio César Perin de; Botaro, Vagner Roberto; Melo, Tânia Márcia Sacramento; Gil, Rossimiriam Pereira de Freitas; Gil, Laurent Frédéric

    2007-01-01

    This work describes the preparation of new chelating materials derived from sugarcane bagasse for adsorption of heavy metal ions in aqueous solution. The first part of this report deals with the chemical modification of sugarcane bagasse with succinic anhydride. The carboxylic acid functions introduced into the material were used to anchor polyamines, which resulted in two yet unpublished modified sugarcane bagasse materials. The obtained materials were characterized by elemental analysis and...

  6. 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.

  7. Recovery of metals from simulant spent lithium-ion battery as organophosphonate coordination polymers in aqueous media.

    Science.gov (United States)

    Perez, Emilie; Andre, Marie-Laure; Navarro Amador, Ricardo; Hyvrard, François; Borrini, Julien; Carboni, Michaël; Meyer, Daniel

    2016-11-05

    An innovative approach is proposed for the recycling of metals from a simulant lithium-ion battery (LIBs) waste aqueous solution. Phosphonate organic linkers are introduced as precipitating agents to selectively react with the metals to form coordination polymers from an aqueous solution containing Ni, Mn and Co in a hydrothermal process. The supernatant is analyzed by ICP-AES to quantify the efficiency and the selectivity of the precipitation and the materials are characterized by Scanning Electron Microscopy (SEM), Powder X-Ray Diffraction (PXRD), Thermogravimetric Analyses (TGA) and nitrogen gas sorption (BET). Conditions have been achieved to selectively precipitate Manganese or Manganese/Cobalt from this solution with a high efficiency. This work describes a novel method to obtain potentially valuable coordination polymers from a waste metal solution that can be generalized on any waste solution. Copyright © 2016 Elsevier B.V. All rights reserved.

  8. Reflection of low energy plasma ions from metal surfaces

    Science.gov (United States)

    Cuthbertson, J. W.; Langer, W. D.; Motley, R. W.

    1992-12-01

    Reflection of low energy (beam source based on acceleration and reflection of ions from a magnetically confined coaxial rf plasma source. The beam provides a large enough ion flux (over 4 A) to allow the characteristics of the reflected neutrals to be measured despite the inefficiency of detection. The energy distributions are measured by means of an electrostatic cylindrical mirror analyzer coupled with a quadrupole mass spectrometer. Energy distributions have been measured for oxygen, nitrogen and inert gas ions incident with from 10 to 70 eV reflected from amorphous metal surfaces of several compositions. The characteristics of particle reflection are commonly predicted in plasma modelling by use of simulation codes based on data from much higher incident energies. Measurements on this beam source allow the assumptions and approximations used in such codes to be tested. The predictions of the widely used TRIM code are compared to measured reflected energy distributions at low incident energies; significant differences are observed, particularly for lower target/projectile atomic mass ratios. The adequacy of the sequential binary collision approximation (used by TRIM) for modelling a collision process which at low energies is actually a simultaneous interaction between several atoms is tested by comparison with n-body trajectory calculations.

  9. 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. 

  10. 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.

  11. 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 ...

  12. Ligational behavior of Schiff bases towards transition metal ion and metalation effect on their antibacterial activity

    Science.gov (United States)

    Devi, Jai; Batra, Nisha; Malhotra, Rajesh

    2012-11-01

    New Schiff bases pyrazine-2-carboxylicacid (phenyl-pyridin-2-yl-methylene)-hydrazide (Hpch-bp) HL1 and pyrazine-2-carboxylicacid (pyridin-2-ylmethylene)-hydrazide (Hpch-pc) HL2 derived from condensation of pyrazine carboxylic hydrazide (Hpch) with 2-benzoyl pyridine (bp) or pyridine 2-carbaldehyde (pc) and their transition metal complexes of type ML(1-2)2 have been synthesized, where M = Mn(II), Co(II), Ni(II), Cu(II) and Zn(II). Characterization of ligands and their metal complexes was carried out by elemental analysis, conductimetric studies, magnetic susceptibility, spectroscopic techniques (IR, UV-VIS, NMR, ESR, Mass) and thermogravimetric analysis. The physico-chemical studies revealed octahedral geometry or distorted octahedral geometry around metal ion. These azomethine Schiff base ligands acted as tridentate ? coordinating through carbonyl, azomethine and pyridine nitrogen present in the ligand. The thermodynamic and thermal properties of the complexes have been investigated and it was observed on the basis of these studies that thermal stability of complexes follows the order Mn activity at different concentrations against bacteria viz. Gram positive Bacillus subtilis, Micrococcus luteus and Gram negative Pseudomonas aeruginosa, Pseudomonas mendocina. A marked enhancement in biocidal activity of the ligands under similar experimental conditions was observed as a consequence of coordination with metal ions. The trend of growth inhibition in the complexes was found to be in the order: Cu > Mn > Ni > Co > Zn.

  13. EPR of transition metal ions in NZP ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Yegor`kova, O.; Kryukova-Orlova, A.I. [Univ. of Nizhnii Novgorod (Russian Federation); Stefanovsky, S.V. [SIA Radon, Moscow (Russian Federation)

    1995-12-31

    NZP-ceramics have been produced by different methods such as sol-gel, flux melting and sintering of dry salts or phosphates. Formation of NZP and related phases was confirmed by X-ray diffraction analysis. Electron paramagnetic resonance (EPR) was applied to evaluate a structure positions of paramagnetic ions and nature of radiation-induced centers. EPR responses from transition metal ions Fe{sup 3+} and Mn{sup 2+} with electron configuration 3d{sup 5} (ground state {sup 6}S{sub 5/2}) which occurred as impurities in raw materials were registered in powders of NZP-ceramics. Fine structure arising due to high spin iron complexes is well resolved. A part of Fe{sup 3+} ions substitutes for Zr{sup 4+} and another part of one substitutes for Na{sup +} ions in six-fold coordinated positions. A great value of hyperfine structure (hfs) constant (9.3 mT) shows a high ionic character of Mn-O bonds in the first coordination sphere. A coordination number is close to 6. Fine structure of Mn{sup 2+} ions are not well resolved. A comparison of the spectra of samples containing various alkali cations shows the substitution for cations in series of Li-Na-K-Rb-Cs does not result in fundamental variation in spectra except for CZP ceramics where the response with g=4.3 due to Fe{sup 3+} in strong ligand field rather than response with g=2.0 due to Fe{sup 3+} in weak field is observed. An investigation of some samples doped by 0.1...0.5 mole % of Fe{sup 3+} or Gd{sup 3+} has been carried out and principal spin-Hamiltonian parameters have been determined. The increase of Fe and Gd ions content as compared to impurity substituting for Zr and possibly Na in their own structural positions results in noticeable site distortion. Gamma irradiation of NZP ceramics results in formation of radiation-induced paramagnetic centers connected to phosphorus-oxygen. The nature and concentration of these centers depend on production method. The lowest defect concentration is in hot-pressed ceramics.

  14. [Measurement of chromium and cobalt ions in metal-on-metal total hip arthroplasty].

    Science.gov (United States)

    Durazo-Villanueva, A; Benítez-Garduño, R

    2012-01-01

    New metal-on-metal hip replacement models emerged in the 1990 with modifications of the previous designs and alloys. This led to expect a lesser rate of ion and particle release in the body with the resulting decrease in wear, osteolysis and loosening. To measure blood and urine chromium and cobalt ions in a 28 mm metal-on-metal tribology during the first postoperative year. Blood and urine cobalt and chromium concentrations were measured in 10 patients (13 prostheses) with the atomic absorption method. The etiology was studied and they were functionally assessed with the Harris functional scale. Adverse metal reactions were also assessed. 8 male and 2 female patients, mean age 54.5 years; 6 had primary coxarthrosis, one was post-traumatic, and 3 had avascular necrosis. The final assessment according to the Harris scale was 92 points. Mean blood chromium was 1.26 ng/l, blood cobalt was 1.033 microg/l; (reference values: chromium 1.4 ng/l and cobalt 1.8 microg/l); only one figure, in a female patient, was found to be higher than normal (chromium 21.2 ng/l and cobalt 15.4 microg/l). Mean urine chromium was 0.95 ng/ml, urine cobalt was 0.53 microg/l (Reference values: chromium: 2.0 ng/ml and cobalt 0.5 microg/l). All patients, with the exception of a female patient, were within the normal ranges. No adverse effect was observed in patients with metal implants with a 28 mm tribology.

  15. Metal is not inert: role of metal ions released by biocorrosion in aseptic loosening--current concepts.

    Science.gov (United States)

    Cadosch, Dieter; Chan, Erwin; Gautschi, Oliver P; Filgueira, Luis

    2009-12-15

    Metal implants are essential therapeutic tools for the treatment of bone fractures and joint replacements. The metals and metal alloys used in contemporary orthopedic and trauma surgery are well tolerated by the majority of patients. However, complications resulting from inflammatory and immune reactions to metal implants have been well documented. This review briefly discusses the different mechanisms of metal implant corrosion in the human body, which lead to the release of significant levels of metal ions into the peri-implant tissues and the systemic blood circulation. Additionally, this article reviews the effects of the released ions on bone metabolism and the immune system and discusses their involvement in the pathophysiological mechanisms of aseptic loosening and metal hypersensitivity in patients with metal implants.

  16. Metal cation/anion adsorption on calcium carbonate: Implications to metal ion concentrations in groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Zachara, J.M.; Cowan, C.E.; Resch, C.T.

    1990-05-01

    This chapter evaluates the sorption behavior of metallic ions on specimen calcite as a basis for determining the importance of calcite relative to other subsurface sorbents, such as layer silicates and oxides, in controlling metal ion concentration in calcareous groundwaters. A review of the literature shows the sorption of both metallic cations and anions on calcite over ranges in pH and CO{sub 2} partial pressure to be consistent with a surface-exchange process where cations exchange with surface Ca and anions exchange with surface CO{sub 3}. A general surface-exchange model was developed to account for the effects of Ca and CO{sub 3} concentrations, pH, and calcite surface area on cation and anion sorption onto calcite. The model was applied to recently developed experimental sorption data of Zn and SeO{sub 3} on specimen calcite in equilibrium CaCO{sub 3}(aq) suspensions. The surface-exchange model was able to describe the effects of pH on both cation and anion sorption, and provided good predictions of the effects of variable CO{sub 2}(g) pressure on Zn sorption and of PO{sub 4} on SeO{sub 3} sorption. The surface-exchange model, combined with sorption constants for other phases, was used to calculate Cd sorption to a hypothetical aquifer material containing a mixture of sorbents. The sorbent concentrations were fixed to those expected in groundwater zones. The multi-sorbent calculation documented the importance of calcite as a sorbent for metallic ions in groundwater.93 refs., 18 figs., 5 tabs.

  17. Metal Ions, Not Metal-Catalyzed Oxidative Stress, Cause Clay Leachate Antibacterial Activity

    Science.gov (United States)

    Otto, Caitlin C.; Koehl, Jennifer L.; Solanky, Dipesh; Haydel, Shelley E.

    2014-01-01

    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. PMID:25502790

  18. 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.

  19. 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.

  20. The Relationship of Culture Media Composition and Chemical Composition on Spirulina sp for Metal Ion Adsorbent

    Directory of Open Access Journals (Sweden)

    Hilda Zulkifli

    2016-12-01

    Full Text Available The analysis relationship of Spirulina sp medium with chemical composition has been conducted. Chemical analysis was performed using X-Ray Fluorescence analysis. Furthermore, potention of Spirulina sp as adsorbent of metal ions was analyzed using FTIR spectroscopy. The results showed that metals such as Zn, Fe, Mn, Ca, Cu, and Mo were mainly metals in Spirulina sp. These metals were not correlated with cultivated medium of Spirulina sp. Analysis of potention Spirulina sp as metal ions adsorbent showed that Spirulina sp has functional groups –C=O and –OH as ligand. Intercation of metal ions Cu(II and Cr(III with Spirulina sp indicated that metal ions bond to –C=O functional group.

  1. Metal ion concentrations and semen quality in patients undergoing hip arthroplasty: A prospective comparison between metal-on-metal and metal-on-polyethylene implants.

    Science.gov (United States)

    Chen, Szu-Yuan; Chang, Chih-Hsiang; Hu, Chih-Chien; Chen, Chun-Chieh; Chang, Yu-Han; Hsieh, Pang-Hsin

    2016-03-01

    The widespread usage of metal-on-metal (MoM) articulations in total hip arthroplasty (THA) has been tempered by concerns of increased metal ion production. The purpose of the study is to evaluate the influence of metal ion exposure on semen quality in young male patients undergoing THA. Male patients who were scheduled for unilateral THA and aged between 20 and 45 years were prospectively enrolled. Patients were sorted into MoM and metal-on-polyethylene (MoP) groups with equal case number. Semen and blood metal ion levels were measured and sperm analysis was performed before, 6 months after, and 1 year after surgery. Compared to preoperative baseline, patients (n = 50) in both groups had increased cobalt (Co) and chromium (Cr) concentrations in blood and seminal fluid after surgery. Between-group comparisons at 6 months and 1 year after surgery showed that patients in the MoM group both had a greater Co concentration in blood and semen and a greater Cr concentration in blood and semen. Patients receiving MoM prosthesis had a reduced percentage of morphologically normal sperm, and decreases from the preoperative level (44.7%) were significant at 6 months (36.8%, p = 0.03) and 1 year (33.8%, p = 0.004). Our data shows a significantly greater concentration of metal ion in blood and semen in patients with MoM prosthesis with a reduced percentage of morphologically normal sperm. Despite small effects on sperm quality, some concerns remain. Further studies are necessary to determine sources of metal ion and to investigate effects on male fertility. © 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.

  2. 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.

  3. A Liquid Chromatography Detector for Transition and Rare-Earth Metal Ions Based on a Cupric Ion-Selective Electrode

    Science.gov (United States)

    1981-05-01

    selective Electrode A Transition Metal CuI) Rare Earth Potentiometry Lanthanide Flow-through Electrode 20. ABSTRACT (Continue on reverse side if necessary...Flow Potentiometry with Ion-selective Electrodes ..... . 19 i. Introduction - Ideal Ion-selective Electrodes . ... 19 2. Interferences...detector is less than I pL, creating much less peak broadening than the earlier polarographic detectors (9,10). C. Flow Potentiometry with Ion-Selective

  4. 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.

  5. Surface modification of nanoclays by catalytically active transition metal ions.

    Science.gov (United States)

    Nawani, Pranav; Gelfer, Mikhail Y; Hsiao, Benjamin S; Frenkel, Anatoly; Gilman, Jeffrey W; Khalid, Syed

    2007-09-11

    A unique class of nanoclays was prepared by modification of pristine clays or organoclays (Cloisite C20A) with transition metal ions (TMIs). The composition, structure, morphology and thermal properties of TMI-modified nanoclays were investigated by atomic absorption spectroscopy (AAS), elemental analysis (EA), scanning electron microscopy (SEM), small-angle X-ray scattering (SAXS), wide-angle X-ray diffraction (WAXD), thermal gravimetric analysis (TGA), differential scanning calorimetry (DSC) and X-ray absorption near-edge structure (XANES) spectroscopy. The content of TMIs in modified clays was found to be close to the limiting value of ion exchange capacity. SEM and X-ray results confirmed that TMIs were located between the mineral layers instead of being adsorbed on the surface of clay particles. TGA results indicated that the TMI treatment of organoclays could significantly increase the thermal stability, which was more pronounced in air than in nitrogen. Temperature-resolved SAXS measurements revealed that the presence of TMIs increased the onset temperature of structural degradation. The higher thermal stability of TMI-modified organoclays can be attributed to the change in the thermal degradation mechanism, resulting in a decrease in the yield of volatile products and the formation of char facilitated by the presence of catalytically active TMIs.

  6. Surface Modification of Nanoclays by Catalytically Active Transition Metal Ions

    Energy Technology Data Exchange (ETDEWEB)

    Nawani,P.; Gelfer, M.; Hsiao, B.; Frenkel, A.; Gilman, J.; Khalid, S.

    2007-01-01

    A unique class of nanoclays was prepared by modification of pristine clays or organoclays (Cloisite C20A) with transition metal ions (TMIs). The composition, structure, morphology and thermal properties of TMI-modified nanoclays were investigated by atomic absorption spectroscopy (AAS), elemental analysis (EA), scanning electron microscopy (SEM), small-angle X-ray scattering (SAXS), wide-angle X-ray diffraction (WAXD), thermal gravimetric analysis (TGA), differential scanning calorimetry (DSC) and X-ray absorption near-edge structure (XANES) spectroscopy. The content of TMIs in modified clays was found to be close to the limiting value of ion exchange capacity. SEM and X-ray results confirmed that TMIs were located between the mineral layers instead of being adsorbed on the surface of clay particles. TGA results indicated that the TMI treatment of organoclays could significantly increase the thermal stability, which was more pronounced in air than in nitrogen. Temperature-resolved SAXS measurements revealed that the presence of TMIs increased the onset temperature of structural degradation. The higher thermal stability of TMI-modified organoclays can be attributed to the change in the thermal degradation mechanism, resulting in a decrease in the yield of volatile products and the formation of char facilitated by the presence of catalytically active TMIs.

  7. Metal Ions Removal Using Nano Oxide Pyrolox™ Material

    Science.gov (United States)

    Gładysz-Płaska, A.; Skwarek, E.; Budnyak, T. M.; Kołodyńska, D.

    2017-02-01

    The paper presents the use of Pyrolox™ containing manganese nano oxides used for the removal of Cu(II), Zn(II), Cd(II), and Pb(II) as well as U(VI) ions. Their concentrations were analyzed using the atomic absorption spectrometer SpectrAA 240 FS (Varian) as well as UV-vis method. For this purpose the static kinetic and equilibrium studies were carried out using the batch technique. The effect of solution pH, shaking time, initial metal ion concentrations, sorbent dosage, and temperature was investigated. The equilibrium data were analyzed using the sorption isotherm models proposed by Freundlich, Langmuir-Freundlich, Temkin, and Dubinin-Radushkevich. The kinetic results showed that the pseudo second order kinetic model was found to correlate the experimental data well. The results indicate that adsorption of Cu(II), Zn(II), Cd(II), and Pb(II) as well as U(VI) ions is strongly dependent on pH. The value of pH 4-7 was optimal adsorption. The time to reach the equilibrium was found to be 24 h, and after this time, the sorption percentage reached about 70%. Kinetics of Cu(II), Zn(II), Cd(II), Pb(II), and U(VI) adsorption on the adsorbent can be described by the pseudo second order rate equation. Nitrogen adsorption/desorption, infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) measurements for adsorbent characterization were performed. Characteristic points of the double layer determined for the studied Pyrolox™ sample in 0.001 mol/dm3 NaCl solution are pHPZC = 4 and pHIEP < 2.

  8. Evaluation of Metal Ion Concentration in Hard Tissues of Teeth in Residents of Central Poland

    Directory of Open Access Journals (Sweden)

    Piotr Wychowanski

    2017-01-01

    Full Text Available Objectives. The aim of the study was an assessment of the content of trace elements in enamel and dentin of teeth extracted in patients residing in urban and agricultural areas of Poland. Methods. The study included 30 generally healthy patients with retained third molars. 65 samples of enamel and dentin from individuals living in urban areas and 85 samples of enamel and dentin from individuals living in agricultural areas were prepared. The content of manganese, lead, cadmium, and chromium in the studied enamel and dentin samples from retained teeth was determined by Graphite Furnace Atomic Absorption Spectrometry. In the process of statistical hypothesis testing, the level of significance was assumed at α=0.05. Results. A comparative analysis of the data showed that enamel and dentin of inhabitants of industrialized areas contain significantly higher amounts of lead and cadmium than hard tissues of teeth in residents of agricultural areas and comparable amounts of manganese and chromium. Significance. It appears that hard tissues of retained teeth may constitute valuable material for assessment of long-term environmental exposure to metal ions. The study confirms that the risk of exposure to heavy metals depends on the place of residence and environmental pollution.

  9. The removal of heavy metal ions from aqueous solutions using sour ...

    African Journals Online (AJOL)

    STORAGESEVER

    2008-12-17

    Dec 17, 2008 ... Key words: Toxic, heavy metal, ions, synthetic, adsorption, biosorption. INTRODUCTION ... heavy metal ions by sour sop seeds from synthetic waste .... Freeland GN, Hoskinson RN, Mayfield RJ (1974). Adsorption of mercury from aqueous solutions by polyethylenamine - modified wood fibers. Environ. Sci.

  10. Alzheimer’s disease: How metal ions define β-amyloid function

    DEFF Research Database (Denmark)

    Kepp, Kasper Planeta

    2017-01-01

    Alzheimer’s disease is increasingly recognized to be linked to the function and status of metal ions, and recently, the amyloid hypothesis has been strongly intertwined with the metal ion hypothesis; in fact, these two hypotheses fit well together and are not mutually contradictory. This review...

  11. Metal-ion dependent catalytic properties of Sulfolobus solfataricus class II α-mannosidase

    DEFF Research Database (Denmark)

    Nielsen, Jonas Willum; Poulsen, Nina Rødtness; Johnsson, Anna Margit Susanne

    2012-01-01

    The active site for the family GH38 class II α-mannosidase is constituted in part by a divalent metal ion, mostly Zn(2+), as revealed in the crystal structures of enzymes from both animal and bacterial sources. The metal ion coordinates to the bound substrate and side chains of conserved amino ac...

  12. Effects of Lability of Metal Complex on Free Ion Measurement Using DMT

    NARCIS (Netherlands)

    Weng, L.P.; Riemsdijk, van W.H.; Temminghoff, E.J.M.

    2010-01-01

    Very low concentrations of free metal ion in natural samples can be measured using the Donnan membrane technique (DMT) based on ion transport kinetics. In this paper, the possible effects of slow dissociation of metal complexes on the interpretation of kinetic DMT are investigated both theoretically

  13. Measuring free metal ion concentrations in multicomponent solutions using Donnan Membrane Technique

    NARCIS (Netherlands)

    Kalis, E.J.J.; Temminghoff, E.J.M.; Weng, L.P.; Riemsdijk, van W.H.

    2007-01-01

    Among speciation techniques that are able to measure free metal ion concentrations, the Donnan membrane technique (DMT) has the advantage that it can measure many different free metal ion concentrations simultaneously in a multicomponent sample. Even though the DMT has been applied to several

  14. Electromigration study of focused ion beam modified metal lines

    Energy Technology Data Exchange (ETDEWEB)

    Lee, J.L.; Yao, D.H. [IBM Microelectronics Div., Essex Junction, VT (United States)

    1995-12-31

    Focus ion beam (FIB) technology is a commonly used tool for integrated circuit device modification, failure analysis, and a variety of other applications. However, limited reliability data of FIB altered circuit is available. This study describes the electromigration mechanism of FIB-altered Al(Cu-Si)/Ti-layered metal lines. The electromigration failures encountered resulted in Al voids at the anode end of FIB-deposited W and Al{sub 2}Cu precipitates at the cathode end. A higher frequency of Al extrusions was also observed on samples stressed at higher temperatures. These observations indicated that FIB-W was an effective blocking boundary for Al and Cu, and confirmed that Cu does electromigrate before Al. The electromigration mechanism of the FIB-altered line closely resembles the published results from two-level Al/W-line/stud interconnect studies. An activation energy of 0.66 eV, with a current exponent of 1.9 and a lognormal sigma of 0.55, was determined from the kinetic analysis of the FIB-altered metal line.

  15. Polyazulene based materials for heavy metal ions detection

    Science.gov (United States)

    Oprisanu, A.; Ungureanu, E. M.; Isopescu, R.; Birzan, L.; Mihai, M.; Vasiliu, C.

    2017-06-01

    Azulene is a special monomer used to functionalize electrodes, due to its spontaneous electron drift from the seven-membered ring to the five-membered ring. The seven-membered ring of the molecule may act as electron acceptor, while the five-membered ring - as electron donor. This leads to very attractive properties for the synthesis of functional advanced materials like: materials with nonlinear optical and photorefractive properties, cathode materials for lithium batteries, or light emitting diodes based on organic materials. Azulene derivatives have been used rarely to the metal ions electroanalysis. Our study concerns the synthesis and electrochemical characterization of a new azulene based monomer 4-(azulen-1-yl)-2,6-bis((E)-2-(thiophen-3-yl)vinyl)pyridine (L). L has been used to obtain modified electrodes by electrochemical polymerization. PolyL films modified electrodes have been characterized by cyclic voltammetry in ferrocene solutions. The complexing properties of polyL based functional materials have been investigated towards heavy metals (Pb, Cd Hg, Cu) by preconcentration - anodic stripping technique in order to analyze the content of these cations from water samples.

  16. Effect of metal ions on Trichophyton rubrum culture

    Energy Technology Data Exchange (ETDEWEB)

    Chandra, A.K.; Banerjee, A.B.

    1975-01-01

    The mycelial growth of Trichophyton rubrum in a synthetic medium comprised of glucose, glutamic acid and salt mixture, could be correlated with the concentration of Fe/sup + +/, Zn/sup + +/, and Mn/sup + +/ up to the concentration 2.5 ..mu..g, 0.5 ..mu..g, and 0.05 ..mu..g/ml respectively. At higher concentrations these metal ions are growth inhibitory. In Zn/sup + +/ and Mn/sup + +/ deficient media, pH was reduced during the growth of the organism. Lactic acid was identified and found responsible for this shift. The culture of the organism under mineral deficiency is characteristically devoid of differentiated reproductive bodies. Ag/sup +/, Bi/sup + + +/, Ba/sup + +/ and Hg/sup + +/ are not growth inhibitory for T. rubrum in complex medium up to a dose level of 20 ppm. The organism is very sensitive to the toxic action of Pb/sup + +/, Cu/sup + +/ and Cd/sup + +/. The culture characteristics of the organism are changed in the presence of heavy metals even at subtoxic dose. 7 references, 2 figures, 2 tables.

  17. Porous metal oxide microspheres from ion exchange resin

    Science.gov (United States)

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

    2015-07-01

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

  18. Role of metal ions in the destruction of TATP: theoretical considerations.

    Science.gov (United States)

    Dubnikova, Faina; Kosloff, Ronnie; Oxley, Jimmie C; Smith, James L; Zeiri, Yehuda

    2011-09-29

    The safe decomposition of solid TATP (triacetone triperoxide) explosive is examined theoretically. The route to destruction starts with formation of metal complexes between a metal ion and the TATP molecule. The second step is decomposition of the molecules into stable final products. We examined the structure and stability of both metal ion (including Na(+), Cu(+), Cu(2+), Co(2+), and Zn(2+)) and proton complexes with TATP using quantum chemical calculations at the DFT-PBE0 level of theory. In addition, for each ion complex, we determined the initial steps in the pathway to decomposition together with the associated transition states. We find that the products of decomposition, in particular, acetone, are also stabilized by ion metal complexes. In agreement with experiment, we find the best candidates for metal ion induced decomposition are Cu(2+) and Zn(2+).

  19. Sunflower stalks as adsorbents for the removal of metal ions from wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Sun, G.; Shi, W. [Univ. of California, Davis, CA (United States). Div. of Textiles and Clothing

    1998-04-01

    Sunflower stalks as adsorbents for the removal of metal ions such as copper, cadmium, zinc, and chromium ions in aqueous solutions were studied with equilibrium isotherms and kinetic adsorptions. The maximum adsorptions of four heavy metals are 29.3 mg/g (Cu{sup 2+}), 30.73 mg/g (Zn{sup 2+}), 42.18 mg/g (Cd{sup 2+}), and 25.07 mg/g (Cr{sup 3+}), respectively. Particle sizes of sunflower stalks affected the adsorption of metal ions; the finer size of particles showed better adsorption to the ions. Temperature also plays an interesting role in the adsorption of different metal ions. Copper, zinc, and cadmium exhibited lower adsorption on sunflower stalks at higher temperature, while chromium showed the opposite phenomenon. The adsorption rates of copper, cadmium, and chromium are quite rapid. Within 60 min of operation about 60--80% of these ions were removed from the solutions.

  20. Barcoded materials based on photoluminescent hybrid system of lanthanide ions-doped metal organic framework and silica via ion exchange.

    Science.gov (United States)

    Shen, Xiang; Yan, Bing

    2016-04-15

    A multicolored photoluminescent hybrid system based on lanthanide ions-doped metal organic frameworks/silica composite host has potential in display and barcode applications. By controlling the stoichiometry of the lanthanides via cation exchange, proportional various lanthanide ions are successfully introduced into metal organic frameworks, whose emission intensity is correspondingly proportional to its amount. The resulting luminescent barcodes depend on the lanthanide ions ratios and compositions. Subsequently, the lanthanide ions located in the channels of metal organic frameworks are protected from any interaction with the environment after the modification of silica on the surface. The optical and thermal stability of the hybrid materials are improved for technological application. Copyright © 2016 Elsevier Inc. All rights reserved.

  1. Effect of the formation of EDTA complexes on the diffusion of metal ions in water

    Science.gov (United States)

    Furukawa, Kenji; Takahashi, Yoshio; Sato, Haruo

    2007-09-01

    The diffusion coefficients of aquo metal ions (M z+ ) and their EDTA complexes (M-EDTA ( z-4)+ ) were compared to understand the effect of EDTA complexation on the diffusion of metal ions by the diffusion cell method for Co 2+, Ga 3+, Rb +, Sr 2+, Ag +, Cd 2+, Cs +, Th 4+, UO22+, and trivalent lanthanides. Most studies about ionic diffusion in water have dealt with free ion (hydrated ion). In many cases, however, polyvalent ions are dissolved as complexed species in natural waters. Hence, we need to study the diffusion behavior of complexes in order to understand the diffusion phenomenon in natural aquifer and to measure speciation by diffusive gradient in thin films (DGT), which requires the diffusion coefficients of the species examined. For many ions, the diffusion coefficients of M-EDTA ( z-4)+ are smaller than those of hydrated ions, but the diffusion coefficients of M-EDTA ( z-4)+ are larger than those of hydrated ions for ions with high ionic potentials (Ga 3+ and Th 4+). As a result, the diffusion coefficients of EDTA complexes are similar among various metal ions. In other words, the diffusion of each ion loses its characteristics by the complexation with EDTA. Although the difference is subtle, it was also found that the diffusion coefficients of EDTA complexes increase as the ionic potential increases, which can be explained by the size of the EDTA complex of each metal ion.

  2. Multidiagnostics analysis of ion dynamics in ultrafast laser ablation of metals over a large fluence range

    Energy Technology Data Exchange (ETDEWEB)

    Anoop, K. K.; Polek, M. P.; Bruzzese, R.; Amoruso, S.; Harilal, Sivanandan S.

    2015-02-28

    The ions dynamics in ultrafast laser ablation of metals is studied over a fluence range spanning from the ablation threshold up to ~75 J/cm2 by means of three established diagnostic techniques. Langmuir probe, Faraday cup and spectrally resolved ICCD imaging simultaneously monitor the laser-produced plasma ions produced during ultrafast laser ablation of a copper target. The fluence dependence of ion yield is analyzed observing the occurrence of three different regimes. Moreover, the specific ion yield shows a maximum at about 4-5 J/cm2, followed by a gradual reduction and a transition to a high-fluence regime above ~50 J/cm2. The fluence variation of the copper ions angular distribution is also analyzed, observing a gradual increase of forward peaking of Cu ions for fluences up to ~10 J/cm2. Then, a broader ion component is observed at larger angles for fluences larger than ~10 J/cm2. Finally, an experimental characterization of the ions angular distribution for several metallic targets (Mg, Al, Cr, Fe, Cu, and W) is carried out at a relatively high fluence of ~66 J/cm2. Interestingly, the ion emission from the volatile metals show a narrow forward peaked distribution and a high peak ion yield compared to the refractory metals. Moreover, the width of ion angular distributions presents a striking correlation with the peak ion yield.

  3. Effect of pH, various divalent metal ion and different substrates on ...

    African Journals Online (AJOL)

    EZUGWU ARINZE LINUS

    Key words: Glucoamylase, pH, metal ions, Aspergillus niger, tiger nut starch, amylopectin. ... formation of a nucleophilic hydroxide ion at neutral pH by .... sodium acetate. Each of the reaction mixtures contains 0.5 ml of enzyme solution, 0.5 ml of starch solution (1%) and 1 ml of metal ion solutions (Ca2+, Mg2+, Mn2+, Fe2+, ...

  4. Effects of mixing metal ions on oxidative DNA damage mediated by a Fenton-type reduction.

    Science.gov (United States)

    Moriwaki, Hiroshi; Osborne, Martin R; Phillips, David H

    2008-02-01

    The formation of 8-hydroxy-deoxyguanosine (8-OHdG) and strand breaks in DNA by Fenton-type reactions by mixtures of two of five metal ions, iron (II), cadmium (II), nickel (II), chromium (III) or copper (II), has been investigated and compared to their formation by each single metal ion. Salmon sperm DNA and pBluescript K+ plasmid were each incubated with hydrogen peroxide and metal ions. The formation of 8-OHdG declined in the Fe (II) or Cu (II) Fenton reaction upon addition of Cd (II) or Ni (II) ion. In contrast, the Fe (II) reaction upon addition of Cr (III) ion showed an additive influence on the formation of 8-OHdG. Furthermore, the Cu (II) plus Cr (III) reaction showed a synergistic effect. These influences relate to the interaction of metal ions with DNA, the potentials of the metal ions to generate activated oxygen and electron transfer between metal ions. The formation of DNA strand breaks was investigated in plasmid DNA by agarose gel electrophoresis and subsequent densitometry. The formation of DNA strand breaks in the Fe (II) or Cu (II) Fenton reaction decreased upon the addition of Ni (II) ion, as with the formation of 8-OHdG mediated by these metal ions. On the other hand, the formation of DNA strand breaks in the Fe (II) reaction decreased upon addition of Cr (III) ion, and the Cu (II) plus Cr (III) reaction did not show the synergistic influence on DNA strand breaks. These results suggest that interactions between two metal ions can influence the generation of 8-OHdG and the formation of DNA strand breaks and demonstrate that these lesions can arise by different mechanisms.

  5. The Use of Coordination Chemistry Principles to Control Aggregation Processes of Metal Ions

    OpenAIRE

    Nayak, Sanjit

    2008-01-01

    The research presented in this thesis is based on the use coordination chemistry principles to control aggregation process of metal ions. Two important areas, which are currently being intensely researched, were chosen. Firstly, controlled aggregation of paramagnetic metal ions to produce cooperatively coupled molecule-based magnets was studied. In Chapter 3, the potential ways of producing single-molecule magnets (SMMs) using polyols as ligands and manganese and iron ions as the paramagnetic...

  6. Importance of diffuse metal ion binding to RNA.

    Science.gov (United States)

    Tan, Zhi-Jie; Chen, Shi-Jie

    2011-01-01

    RNAs are highly charged polyanionic molecules. RNA structure and function are strongly correlated with the ionic condition of the solution. The primary focus of this article is on the role of diffusive ions in RNA folding. Due to the long-range nature of electrostatic interactions, the diffuse ions can contribute significantly to RNA structural stability and folding kinetics. We present an overview of the experimental findings as well as the theoretical developments on the diffuse ion effects in RNA folding. This review places heavy emphasis on the effect of magnesium ions. Magnesium ions play a highly efficient role in stabilizing RNA tertiary structures and promoting tertiary structural folding. The highly efficient role goes beyond the mean-field effect such as the ionic strength. In addition to the effects of specific ion binding and ion dehydration, ion-ion correlation for the diffuse ions can contribute to the efficient role of the multivalent ions such as the magnesium ions in RNA folding.

  7. Heterocyclic ring based colorimetric and fluorescent chemosensor for transition metal ions in an aqueous medium

    Energy Technology Data Exchange (ETDEWEB)

    Udhayakumari, Duraisamy [Department of Chemistry, Organic and Polymer Synthesis Laboratory, National Institute of Technology, Tiruchirappalli 620015 (India); Velmathi, Sivan, E-mail: velmathis@nitt.edu [Department of Chemistry, Organic and Polymer Synthesis Laboratory, National Institute of Technology, Tiruchirappalli 620015 (India); Boobalan, Maria susai [Department of Chemistry, St. Joseph' s College (Autonomous), Tiruchirappalli 620002 (India); Venkatesan, Parthiban; Wu, Shu-Pao [Department of Applied Chemistry, National Chiao Tung University, Hsinchu 300, Taiwan, ROC (China)

    2015-02-15

    Heterocyclic ring based R1–R3 have been synthesized from the simple condensation method. R1–R3 exhibit highly selective and sensitive recognition towards transition metal ions in an aqueous medium via visual color change and were further confirmed by UV–vis and fluorescent spectroscopic methods. Fluorescent turn on and turn off behavior was observed for receptors tested with transition metal ions. The interaction of transition metal ions and receptors R1–R3 was confirmed to adopt 1:1 binding stoichiometry. Micromolar detection limit was found for R1–R3 with metal ions. DFT theoretical calculations were employed to understand the sensing mechanism of the sensors towards the metal ions. R1 and R2 were also successfully demonstrated as a fluorescent probe for detecting Cu{sup 2+} ions in living cells. - highlights: • R1–R3 act as colorimetric and fluorescent sensors for metal ions. • Receptors (R1–R3) detect Cu{sup 2+} ions in aqueous solution at nanomolar levels. • R1 and R2 act as a fluorescent probe for detecting Cu{sup 2+} ions in living cells.

  8. Selective retention of basic compounds by metal aquo-ion affinity chromatography.

    Science.gov (United States)

    Asakawa, Yoshiki; Yamamoto, Eiichi; Asakawa, Naoki

    2014-10-01

    A novel metal aquo-ion affinity chromatography has been developed for the analysis of basic compounds using heat-treated silica gel containing hydrated metal cations (metal aquo-ions) as the packing material. The packing materials of the metal aquo-ion affinity chromatography were prepared by the immobilization of a single metal component such as Fe(III), Al(III), Ag(I), and Ni(II) on silica gel followed by extensive heat treatment. The immobilized metals form aquo-ions to present cation-exchange ability for basic analytes and the cation-exchange ability for basic analytes depends on pKa of the immobilized metal species. In the present study, to evaluate the retention characteristics of metal aquo-ion affinity chromatography, the on-line solid-phase extraction of drugs was investigated. Obtained data clearly evidence the selective retention capability of metal aquo-ion affinity chromatography for basic analytes with sufficient capacity. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Metal-on-metal bearings in total hip arthroplasties : Influence of cobalt chromium ions on bacterial growth and biofilm formation

    NARCIS (Netherlands)

    Hosman, Anton H.; van der Mei, Henny C.; Bulstra, Sjoerd K.; Busscher, Henk J.; Neut, Danielle

    2009-01-01

    Metal-on-metal (MOM) bearings involving cobalt-chromium (Co-Cr) alloys in total hip arthroplasties are becoming more and more popular due to their low wear. Consequences of corrosion products of Co-Cr alloys are for the most part unclear, and the influence of cobalt and chromium ions on biofilm

  10. Electrochemical, optical and metal ion sensing properties of dithizone derivatised electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Mirkhalaf, F

    1998-07-01

    Derivatisation of electrode surfaces with ultra-thin films of organic molecules has been extensively studied for many applications in recent years. The present study is based on a new approach in the preparation and use of these electrodes for metal ion sensing. Modification of electrode surfaces with a ligand specific to heavy metal ions has been described. A new derivative of dithizone (DDz) and its secondary metal complexes have been synthesised and attached onto indium tin oxide (ITO) and gold electrodes. This was achieved by covalent bonding between carboxyl groups in DDz and terminal amine groups of molecules self-assembled on the electrode surfaces. These monolayer films were characterised by cyclic voltammetry, by in situ and ex situ surface spectroscopies and by their response to some transition metal ions. Mechanisms for the electrochemical and spectroscopic observations have been proposed. The coordination of heavy metal ions by the DDz film attached on electrode surfaces have been studied for its application as a metal ion sensing element. The uptake and release of metal ions by the ligand on the gold surface were followed by surface techniques and film characterisation was carried out by ellipsometry, Raman and in situ FTIR spectroscopy. A surface plasmon resonance (SPR) device with in situ electrochemical control was designed and constructed. The use of gold electrodes modified with DDz as a sensing element for metal ion detection in the SPR device was studied. Possible applications of these modified electrodes with potential control in metal ion detection are described. The electrochemical and SPR responses for the metal ion sensing by the monolayer films were compared with those of polymer films containing the same ligand. (author)

  11. Metal ions in biological catalysis: from enzyme databases to general principles.

    Science.gov (United States)

    Andreini, Claudia; Bertini, Ivano; Cavallaro, Gabriele; Holliday, Gemma L; Thornton, Janet M

    2008-11-01

    We analysed the roles and distribution of metal ions in enzymatic catalysis using available public databases and our new resource Metal-MACiE (http://www.ebi.ac.uk/thornton-srv/databases/Metal_MACiE/home.html). In Metal-MACiE, a database of metal-based reaction mechanisms, 116 entries covering 21% of the metal-dependent enzymes and 70% of the types of enzyme-catalysed chemical transformations are annotated according to metal function. We used Metal-MACiE to assess the functions performed by metals in biological catalysis and the relative frequencies of different metals in different roles, which can be related to their individual chemical properties and availability in the environment. The overall picture emerging from the overview of Metal-MACiE is that redox-inert metal ions are used in enzymes to stabilize negative charges and to activate substrates by virtue of their Lewis acid properties, whereas redox-active metal ions can be used both as Lewis acids and as redox centres. Magnesium and zinc are by far the most common ions of the first type, while calcium is relatively less used. Magnesium, however, is most often bound to phosphate groups of substrates and interacts with the enzyme only transiently, whereas the other metals are stably bound to the enzyme. The most common metal of the second type is iron, which is prevalent in the catalysis of redox reactions, followed by manganese, cobalt, molybdenum, copper and nickel. The control of the reactivity of redox-active metal ions may involve their association with organic cofactors to form stable units. This occurs sometimes for iron and nickel, and quite often for cobalt and molybdenum.

  12. Electrochemical, optical and metal ion sensing properties of dithizone derivatised electrodes

    CERN Document Server

    Mirkhalaf, F

    1998-01-01

    studied. Possible applications of these modified electrodes with potential control in metal ion detection are described. The electrochemical and SPR responses for the metal ion sensing by the monolayer films were compared with those of polymer films containing the same ligand. Derivatisation of electrode surfaces with ultra-thin films of organic molecules has been extensively studied for many applications in recent years. The present study is based on a new approach in the preparation and use of these electrodes for metal ion sensing. Modification of electrode surfaces with a ligand specific to heavy metal ions has been described. A new derivative of dithizone (DDz) and its secondary metal complexes have been synthesised and attached onto indium tin oxide (ITO) and gold electrodes. This was achieved by covalent bonding between carboxyl groups in DDz and terminal amine groups of molecules self-assembled on the electrode surfaces. These monolayer films were characterised by cyclic voltammetry, by in situ and ex...

  13. Protein C production: metal ion/protein interfacial interaction in immobilized metal affinity chromatography.

    Science.gov (United States)

    Lee, James J; Thiessen, Eileen; Bruley, Duane F

    2005-01-01

    Protein C (PC) is an essential blood factor in the human blood coagulation cascade. PC can help achieve blood hemostasis in many deadly disease conditions such as sepsis, cancer, HIV, etc.; reduced oxygen transport due to blood agglutination within the body can cause tissue death and organ failure as a result of low oxygen transport. Our goal is to produce large quantities of low cost zymogen PC for the treatment and prevention of blood clotting resulting from many disease states, as well as provide an effective therapy for PC deficiency. Current studies show that Immobilized Metal Affinity Chromatography (IMAC) has high specificity and can be used for difficult separations among homologous proteins at relatively low cost compared to current methods, such as Immunoaffinity Chromatography. Thus, we are investigating the optimization of IMAC for the separation and purification of PC from Cohn fraction IV-I. Molecular interactions within the chromatography column involve many parameters that include: the use and type of chromatographic gel and buffer solution, the pH, temperature, metal ion, chelator, and the sequence and structure of the protein itself. These parameters all influence the protein's interaction with the column. Experimental equilibrium isotherms show that PC has primary and secondary binding characteristics, demonstrating that the interaction is not just a simple process of one protein binding to one metal ion. Understanding the thermodynamics of interfacial interaction between proteins and surface-bound Cu2+ is essential to optimizing IMAC for PC purification, as well as for separation of other proteins in general. Hence we are undertaking theoretical and experimental studies of IDA-Cu/PC adsorption. The differences in structures of PC and other critical homologous blood factors are examined using the protein visualization program Cn3D. A better understanding of the interfacial phenomena will help determine the most effective conditions to achieve our

  14. Development of sensitive holographic devices for physiological metal ion detection

    Science.gov (United States)

    Sabad-e.-Gul; Martin, Suzanne; Cassidy, John; Naydenova, Izabela

    2017-08-01

    The development of selective alkali metal ions sensors in particular is a subject of significant interest. In this respect, the level of blood electrolytes, particularly H+, Na+, K+ and Cl- , is widely used to monitor aberrant physiologies associated with pulmonary emphysema, acute and chronic renal failure, heart failure, diabetes. The sensors reported in this paper are created by holographic recording of surface relief structures in a self-processing photopolymer material. The structures are functionalized by ionophores dibenzo-18-crown-6 (DC) and tetraethyl 4-tert-butylcalix[4]arene (TBC) in plasticised polyvinyl chloride (PVC) matrix. Interrogation of these structures by light allows indirect measurements of chemical analytes' concentration in real time. We present results on the optimisation and testing of the holographic sensor. A self-processing acrylamide-based photopolymer was used to fabricate the required photonic structures. The performance of the sensors for detection of K+ and Na+ was investigated. It was observed that the functionalisation with DC provides a selective response of the devices to K+ over Na+ and TBC coated surface structures are selectively sensitive to Na+. The sensor responds to Na+ within the physiological ranges. Normal levels of Na+ and K+ in human serum lie within the ranges 135-148mM and 3.5-5.3 mM respectively.

  15. Multidiagnostic analysis of ion dynamics in ultrafast laser ablation of metals over a large fluence range

    Science.gov (United States)

    Anoop, K. K.; Polek, M. P.; Bruzzese, R.; Amoruso, S.; Harilal, S. S.

    2015-02-01

    The dynamics of ions in ultrafast laser ablation of metals is studied over fluences ranging from the ablation threshold up to ≈75 J/cm2 by means of three well-established diagnostic techniques. Langmuir probe, Faraday cup, and spectrally resolved intensified charge coupled device imaging simultaneously monitored the ions produced during ultrafast laser ablation of a pure copper target with 800 nm, ≈50 fs, Ti: Sapphire laser pulses. The fluence dependence of ion yield is analyzed, resulting in the observance of three different regimes. The specific ion yield shows a maximum at about 4-5 J/cm2, followed by a gradual reduction and a transition to a high-fluence regime above ≈50 J/cm2. The fluence dependence of the copper ions angular distribution is also analyzed, observing a gradual increase in forward-peaking of Cu ions for fluences up to ≈10 J/cm2. A broader ion component is observed at larger angles for fluences larger than ≈10 J/cm2. Finally, an experimental characterization of the ionic angular distribution for several metallic targets (Mg, Al, Cr, Fe, Cu, and W) is carried out at a relatively high fluence of ≈66 J/cm2. Interestingly, the ion emission from the volatile metals shows a narrow, forward-peaked distribution, and a high peak ion yield compared to the refractory metals. Moreover, the width of ionic angular distributions presents a striking correlation with the peak ion yield.

  16. MCTBI: a web server for predicting metal ion effects in RNA structures.

    Science.gov (United States)

    Sun, Li-Zhen; Zhang, Jing-Xiang; Chen, Shi-Jie

    2017-08-01

    Metal ions play critical roles in RNA structure and function. However, web servers and software packages for predicting ion effects in RNA structures are notably scarce. Furthermore, the existing web servers and software packages mainly neglect ion correlation and fluctuation effects, which are potentially important for RNAs. We here report a new web server, the MCTBI server (http://rna.physics.missouri.edu/MCTBI), for the prediction of ion effects for RNA structures. This server is based on the recently developed MCTBI, a model that can account for ion correlation and fluctuation effects for nucleic acid structures and can provide improved predictions for the effects of metal ions, especially for multivalent ions such as Mg2+ effects, as shown by extensive theory-experiment test results. The MCTBI web server predicts metal ion binding fractions, the most probable bound ion distribution, the electrostatic free energy of the system, and the free energy components. The results provide mechanistic insights into the role of metal ions in RNA structure formation and folding stability, which is important for understanding RNA functions and the rational design of RNA structures. © 2017 Sun et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society.

  17. A review on various electrochemical techniques for heavy metal ions detection with different sensing platforms.

    Science.gov (United States)

    Bansod, BabanKumar; Kumar, Tejinder; Thakur, Ritula; Rana, Shakshi; Singh, Inderbir

    2017-08-15

    Heavy metal ions are non-biodegradable and contaminate most of the natural resources occurring in the environment including water. Some of the heavy metals including Lead (Pb), Mercury (Hg), Arsenic (As), Chromium (Cr) and Cadmium (Cd) are considered to be highly toxic and hazardous to human health even at trace levels. This leads to the requirement of fast, accurate and reliable techniques for the detection of heavy metal ions. This review presents various electrochemical detection techniques for heavy metal ions those are user friendly, low cost, provides on-site and real time monitoring as compared to other spectroscopic and optical techniques. The categorization of different electrochemical techniques is done on the basis of different types of detection signals generated due to presence of heavy metal ions in the solution matrix like current, potential, conductivity, electrochemical impedance, and electrochemiluminescence. Also, the recent trends in electrochemical detection of heavy metal ions with various types of sensing platforms including metals, metal films, metal oxides, nanomaterials, carbon nano tubes, polymers, microspheres and biomaterials have been evoked. Copyright © 2017 Elsevier B.V. All rights reserved.

  18. Metal ion enhanced binding of AMD3100 to Asp262 in the CXCR4 receptor

    DEFF Research Database (Denmark)

    Gerlach, Lars Ole; Jakobsen, Janus S; Jensen, Kasper P

    2003-01-01

    of the bicyclam is dependent on both Asp(171) and Asp(262), the enhancing effect of the metal ion was selectively eliminated by substitution of Asp(262) located at the extracellular end of TM-VI. It is concluded that the increased binding affinity of the metal ion substituted AMD3100 is obtained through enhanced...... interaction of one of the cyclam ring systems with the carboxylate group of Asp(262). It is suggested that this occurs through a strong concomitant interaction of one of the oxygen's directly with the metal ion and the other oxygen to one of the nitrogens of the cyclam ring through a hydrogen bond....

  19. Studies on calcium phosphate precipitation: effects of metal ions used in dental materials.

    Science.gov (United States)

    Okamoto, Y; Hidaka, S

    1994-12-01

    The effects of 26 metal ions, of which 23 are used in dental materials, on the conversion of amorphous calcium phosphate (ACP) to hydroxyapatite (HAP) in vitro were studied. From the effects on both the rate of HAP transformation and induction time, effects of metal ions were classified into three types; inhibitory (in the order: nickel, tin, cobalt, manganese, copper, zinc, gallium, thallium, molybdenum, cadmium, antimony, magnesium, and mercury); ineffective (cesium, titanium, chromium, iron [ferrous], iridium, palladium, platinum, silver, gold, aluminum, and lead); and stimulatory (iron [ferric] and indium). These results suggest that metal ions used in dental materials may modify the precipitation of oral calcium phosphate.

  20. Ion exchange system design for removal of heavy metals from acid mine drainage wastewater

    Directory of Open Access Journals (Sweden)

    R. S. Sapkal

    2010-11-01

    Full Text Available This paper discusses the methodology used to determine the optimal ion-exchange column size to process all separate batchesof feeds from acid mine drainage wastewater.The optimal design ensures the best utilization of resin material and therefore results in a minimum amount of spent resins.Ion exchanger materials have been studied for removing heavy metals from a metal bearing wastes. For the current treatment,a facility has been designed for the removal of heavy metals from the acid mine drainage (AMD waste by the ion-exchange technology.

  1. On the single-ion Magnetic Anisotropy of the Rare-Earth Metals

    DEFF Research Database (Denmark)

    Kolmakova, N.P.; Tishin, A.M.; Bohr, Jakob

    1996-01-01

    The temperature dependences of the single-ion magnetic anisotropy constants for Tb and Dy metals are calculated in terms of the multipole moments of the rare-earth ions utilizing the available crystal-field parameters. The results are compared with the existing experimental data.......The temperature dependences of the single-ion magnetic anisotropy constants for Tb and Dy metals are calculated in terms of the multipole moments of the rare-earth ions utilizing the available crystal-field parameters. The results are compared with the existing experimental data....

  2. Nanodiamonds act as Trojan horse for intracellular delivery of metal ions to trigger cytotoxicity.

    Science.gov (United States)

    Zhu, Ying; Zhang, Yu; Shi, Guosheng; Yang, Jinrong; Zhang, Jichao; Li, Wenxin; Li, Aiguo; Tai, Renzhong; Fang, Haiping; Fan, Chunhai; Huang, Qing

    2015-02-05

    Nanomaterials hold great promise for applications in the delivery of various molecules with poor cell penetration, yet its potential for delivery of metal ions is rarely considered. Particularly, there is limited insight about the cytotoxicity triggered by nanoparticle-ion interactions. Oxidative stress is one of the major toxicological mechanisms for nanomaterials, and we propose that it may also contribute to nanoparticle-ion complexes induced cytotoxicity. To explore the potential of nanodiamonds (NDs) as vehicles for metal ion delivery, we used a broad range of experimental techniques that aimed at getting a comprehensive assessment of cell responses after exposure of NDs, metal ions, or ND-ion mixture: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, Trypan blue exclusion text, optical microscope observation, synchrotron-based scanning transmission X-ray microscopy (STXM) and micro X-ray fluorescence (μXRF) microscopy, inductively coupled plasma-mass spectrometry (ICP-MS), reactive oxygen species (ROS) assay and transmission electron microscopy (TEM) observation. In addition, theoretical calculation and molecular dynamics (MD) computation were used to illustrate the adsorption properties of different metal ion on NDs as well as release profile of ion from ND-ion complexes at different pH values. The adsorption capacity of NDs for different metal ions was different, and the adsorption for Cu2+ was the most strong among divalent metal ions. These different ND-ion complexes then had different cytotoxicity by influencing the subsequent cellular responses. Detailed investigation of ND-Cu2+ interaction showed that the amount of released Cu2+ from ND-Cu2+ complexes at acidic lysosomal conditions was much higher than that at neutral conditions, leading to the elevation of intracellular ROS level, which triggered cytotoxicity. By theoretical approaches, we demonstrated that the functional carbon surface and cluster structures of NDs made them

  3. Metal ion concentrations in body fluids after implantation of hip replacements with metal-on-metal bearing--systematic review of clinical and epidemiological studies.

    Directory of Open Access Journals (Sweden)

    Albrecht Hartmann

    Full Text Available INTRODUCTION: The use of metal-on-metal (MoM total hip arthroplasty (THA increased in the last decades. A release of metal products (i.e. particles, ions, metallo-organic compounds in these implants may cause local and/or systemic adverse reactions. Metal ion concentrations in body fluids are surrogate measures of metal exposure. OBJECTIVE: To systematically summarize and critically appraise published studies concerning metal ion concentrations after MoM THA. METHODS: Systematic review of clinical trials (RCTs and epidemiological studies with assessment of metal ion levels (cobalt, chromium, titanium, nickel, molybdenum in body fluids after implantation of metalliferous hip replacements. Systematic search in PubMed and Embase in January 2012 supplemented by hand search. Standardized abstraction of pre- and postoperative metal ion concentrations stratified by type of bearing (primary explanatory factor, patient characteristics as well as study quality characteristics (secondary explanatory factors. RESULTS: Overall, 104 studies (11 RCTs, 93 epidemiological studies totaling 9.957 patients with measurement of metal ions in body fluids were identified and analyzed. Consistently, median metal ion concentrations were persistently elevated after implantation of MoM-bearings in all investigated mediums (whole blood, serum, plasma, erythrocytes, urine irrespective of patient characteristics and study characteristics. In several studies very high serum cobalt concentrations above 50 µg/L were measured (detection limit typically 0.3 µg/L. Highest metal ion concentrations were observed after treatment with stemmed large-head MoM-implants and hip resurfacing arthroplasty. DISCUSSION: Due to the risk of local and systemic accumulation of metallic products after treatment with MoM-bearing, risk and benefits should be carefully balanced preoperatively. The authors support a proposed "time out" for stemmed large-head MoM-THA and recommend a restricted

  4. MINAS--a database of Metal Ions in Nucleic AcidS.

    Science.gov (United States)

    Schnabl, Joachim; Suter, Pascal; Sigel, Roland K O

    2012-01-01

    Correctly folded into the respective native 3D structure, RNA and DNA are responsible for uncountable key functions in any viable organism. In order to exert their function, metal ion cofactors are closely involved in folding, structure formation and, e.g. in ribozymes, also the catalytic mechanism. The database MINAS, Metal Ions in Nucleic AcidS (http://www.minas.uzh.ch), compiles the detailed information on innersphere, outersphere and larger coordination environment of >70,000 metal ions of 36 elements found in >2000 structures of nucleic acids contained today in the PDB and NDB. MINAS is updated monthly with new structures and offers a multitude of search functions, e.g. the kind of metal ion, metal-ligand distance, innersphere and outersphere ligands defined by element or functional group, residue, experimental method, as well as PDB entry-related information. The results of each search can be saved individually for later use with so-called miniPDB files containing the respective metal ion together with the coordination environment within a 15 Å radius. MINAS thus offers a unique way to explore the coordination geometries and ligands of metal ions together with the respective binding pockets in nucleic acids.

  5. Effects of metal ions on proliferation of aortic smooth muscle cells and myoblastic cells in vitro

    Energy Technology Data Exchange (ETDEWEB)

    Vorpahl, M.; Wiemann, M.; Bingmann, D. [Essen Univ. (Germany). Inst. fuer Physiologie; Brauer, H. [Werkstofftechnik, Univ. Essen (Germany)

    2001-12-01

    Metal ions released from implanted stents into the surrounding tissue may contribute to vascular reactions which cause restenosis in about 30%. This assumption prompted us to investigate short term effects of metal ions (Ag, Al, Cr, Fe, Mo, Ni, V, all applied as chloride salts) on proliferation of swine aortic smooth muscle cells (SMC) and a myoblastic cell line (C2C12). Cell confluence was 30 or 50% when metal ions were added and cell growth was monitored with the MTT-test after 2 days. A clear concentration dependence of acute toxicity of the different metal ions was found for both cell types. The order of toxicity indicated by IC50 values was V > Ni > Fe > Mo > Al > Cr. The nearly insoluble silverchloride exerted unclear effects. In experiments starting at high confluence, the apparent toxicity of Fe, Ni, and V was reduced. Al, which to our knowledge is not a major constituent in medical stents, was the only metal ion found here to cause a slightly increased proliferation, but this effect was restricted to the low concentration range (16-250 {mu}mol/l). In general, results for both cell types, C2C12 and SMC, were very similar. We conclude that short term effects of metal ions, which may be released in the interface of stent and vessel wall tissue, comprise a reduction rather than a stimulation of cell proliferation. However, restenosis may be initiated as a complex tissue reaction to primary toxic metal effects. (orig.)

  6. Further insights into the metal ion binding abilities and the metalation pathway of a plant metallothionein from Musa acuminata.

    Science.gov (United States)

    Cabral, Augusto C S; Jakovleska, Jovana; Deb, Aniruddha; Penner-Hahn, James E; Pecoraro, Vincent L; Freisinger, Eva

    2017-12-07

    The superfamily of metallothioneins (MTs) combines a diverse group of metalloproteins, sharing the characteristics of rather low molecular weight and high cysteine content. The latter provides MTs with the capability to coordinate thiophilic metal ions, in particular those with a d 10 electron configuration. The sub-family of plant MT3 proteins is only poorly characterized and there is a complete lack of three-dimensional structure information. Building upon our previous results on the Musa acuminata MT3 (musMT3) protein, the focus of the present work is to understand the metal cluster formation process, the role of the single histidine residue present in musMT3, and the metal ion binding affinity. We concentrate our efforts on the coordination of ZnII and CdII ions, using CoII as a spectroscopic probe for ZnII binding. The overall protein-fold is analysed with a combination of limited proteolytic digestion, mass spectrometry, and dynamic light scattering. Histidine coordination of metal ions is probed with extended X-ray absorption fine structure spectroscopy and CoII titration experiments. Initial experiments with isothermal titration calorimetry provide insights into the thermodynamics of metal ion binding.

  7. Importance of Diffuse Metal Ion Binding to RNA

    Science.gov (United States)

    Tan, Zhi-Jie; Chen, Shi-Jie

    2016-01-01

    RNAs are highly charged polyanionic molecules. RNA structure and function are strongly correlated with the ionic condition of the solution. The primary focus of this article is on the role of diffusive ions in RNA folding. Due to the long-range nature of electrostatic interactions, the diffuse ions can contribute significantly to RNA structural stability and folding kinetics. We present an overview of the experimental findings as well as the theoretical developments on the diffuse ion effects in RNA folding. This review places heavy emphasis on the effect of magnesium ions. Magnesium ions play a highly efficient role in stabilizing RNA tertiary structures and promoting tertiary structural folding. The highly efficient role goes beyond the mean-field effect such as the ionic strength. In addition to the effects of specific ion binding and ion dehydration, ion-ion correlation for the diffuse ions can contribute to the efficient role of the multivalent ions such as the magnesium ions in RNA folding. PMID:22010269

  8. The impacts of common ions on the adsorption of heavy metal

    Science.gov (United States)

    He, Jiang; Xue, Hong-Xi; Lü, Chang-Wei; Fan, Qing-Yun; Liang, Ying; Sun, Ying; Shen, Li-Li; Bai, Saruli

    2009-10-01

    Researches on the impact of common ions onto sediments are of great importance for the study of the heavy metal adsorption mechanisms. Considering the surface sediments from the relatively clean reach in the Baotou section of the Yellow River as the adsorbent, this work presents the impacts of common ions (Na+, Mg2+, K+, Ca2+, Cl-, SO4 2-, and NH4 +) on heavy metals (Cu2+, Zn2+, Cd2+, and Pb2+) adsorption. The experimental results reveal that the adsorptive capacities of the heavy metals are controlled by different adsorption mechanisms in different ion concentration ranges. With the increase of the ionic strength, the adsorption of the heavy metals increases for the compression of the electric double layer, whereas decreases for the decreasing of the ionic activities of the heavy metals. The competitive adsorption and complexations between the heavy metals and common ions are also important factors controlling the heavy metal adsorption. According to the experimental results and the real concentration of common ions in the Baotou section of the Yellow River, the increase of the concentrations of Na+, Mg2+, K+, and Ca2+ would cause the increase of Zn2+ adsorption and reduce the Zn pollution. The NH4 + from the industrial discharge of the tributaries has a strong impact on the heavy metal adsorption.

  9. Factors controlling the reactivity of divalent metal ions towards pheophytin a.

    Science.gov (United States)

    Orzeł, Ł; Waś, J; Kania, A; Susz, A; Rutkowska-Zbik, D; Staroń, J; Witko, M; Stochel, G; Fiedor, L

    2017-08-01

    In this study, we evaluate the factors which determine the reactivity of divalent metal ions in the spontaneous formation of metallochlorophylls, using experimental and computational approaches. Kinetic studies were carried out using pheophytin a in reactions with various divalent metal ions combined with non- or weakly-coordinative counter ions in a series of organic solvents. To obtain detailed insights into the solvent effect, the metalations with the whole set of cations were investigated in three solvents and with Zn2+ in seven solvents. The reactions were monitored using electronic absorption spectroscopy and the stopped-flow technique. DFT calculations were employed to shed light on the role of solvent in activating the metal ions towards porphyrinoids. This experimental and computational analysis gives detailed information regarding how the solvent and the counter ion assist/hinder the metalation reaction as activators/inhibitors. The metalation course is dictated to a large extent by the reaction medium, via either the activation or deactivation of the incoming metal ion. The solvent may affect the metalation in several ways, mainly via H-bonding with pyrrolenine nitrogens and the activation/deactivation of the incoming cation. It also seems to affect the activation enthalpy by causing slight conformational changes in the macrocyclic ligand. These new mechanistic insights contribute to a better understanding of the "metal-counterion-solvent" interplay in the metalation of porphyrinoids. In addition, they are highly relevant to the mechanisms of metalation reactions catalyzed by chelatases and explain the differences between the insertion of Mg2+ and other divalent cations.

  10. Determination of metal ions by high-performance liquid chromatographic separation of their hydroxamic acid chelates

    Energy Technology Data Exchange (ETDEWEB)

    Palmieri, M.D.; Fritz, J.S.

    1987-09-15

    Metal ions are determined by adding N-methylfurohydroxamic acid to an aqueous sample and then separating the metal chelates by direct injection onto a liquid chromatographic column. Separations on a C/sub 8/ silica column and a polystyrene-divinylbenzene column are compared, with better separations seen on the polymeric column. The complexes formed at low pH values are cationic and are separated by an ion pairing mechanism. Retention times and selectivity of the metal complexes can be varied by changing the pH. Several metal ions can be separated and quantified; separation conditions, linear calibration curve ranges, and detection limits are presented for Zr(IV), Hf(IV), Fe(III), Nb(V), Al(III), and Sb(III). Interferences due to the presence of other ions in solution are investigated. Finally, an antiperspirant sample is analyzed for zirconium by high-performance liquid chromatography.

  11. Cross-Reactive Sensor Array for Metal Ion Sensing Based on Fluorescent SAMs

    NARCIS (Netherlands)

    Basabe Desmonts, M.L.; van der Baan, Frederieke; Zimmerman, R.S.; Reinhoudt, David; Crego Calama, Mercedes

    2007-01-01

    Fluorescent self assembled monolayers (SAMs) on glass were previouslydeveloped in our group as new sensing materials for metal ions. These fluorescent SAMs arecomprised by fluorophores and small molecules sequentially deposited on a monolayer onglass. The preorganization provided by the surface

  12. Process for the conversion of sugars to lactic acid and 2-hydroxy-3-butenoic acid or esters thereof comprising a metallo-silicate material and a metal ion

    DEFF Research Database (Denmark)

    2015-01-01

    A process for the preparation of lactic acid and 2-hydroxy- 3-butenoic acid or esters thereof from a sugar in the presence of a metallo-silicate material, a metal ion and a solvent, wherein the metal ion is selected from one or more of the group consisting of potassium ions, sodium ions, lithium...... ions, rubidium ions and caesium ions....

  13. Occurrence of metal ions in rice produced in Uruguay

    Directory of Open Access Journals (Sweden)

    Mario Rivero

    2011-04-01

    Full Text Available The United Nations General Assembly declared the year 2004 the International Year of Rice under the concept "Rice is Life". The largest nutritional problems occurring globally are protein-energy malnutrition, Ca, Fe, I, Zn and vitamin A deficiencies. Being rice the staple food more consumed worldwide, outstanding care is taken on its composition levels.Uruguay has emerged as medium-size rice producer and Latin America's major rice exporter, and is now amongst the world's top ten. Thus, the knowledge of toxic as well as micronutrient elements is very important. Here is reported the determination in forty nine samples of rice (Oryza sativa L. of As, Cd, Cr, and Pb by ET AAS in samples digested by dry ashing, and Ca, Co, Cu, Fe, K, Mg, Mo, Mn, Na, Ni and Zn by FAAS and Hg by CV AAS using microwave-assisted decomposition.The amount of all the metal ions studied in this work fall within the range typical of rice around the world. All the rice samples tested showed lower levels of As, Cd, Hg and Pb than the maximum limit permitted by governmental and international organizations.Potassium was the most abundant mineral followed by Mg and Ca and amongst microelements the presence of Cu, Fe, Mo, Mn, Na and Zn was outstanding.The milling process highly affects the contents of K, Mg, Mn, Na and Zn while little influence has on Ca, Co, Cu and Fe concentrations.Unexpected loss of Ca, Fe and Mn during parboiling process was detected. 

  14. Silica coated magnetite nanoparticles for removal of heavy metal ions from polluted waters

    CERN Document Server

    Dash, Monika

    2013-01-01

    Magnetic removal of Hg2+ and other heavy metal ions like Cd2+, Pb2+ etc. using silica coated magnetite particles from polluted waters is a current topic of active research to provide efficient water recycling and long term high quality water. The technique used to study the bonding characteristics of such kind of nanoparticles with the heavy metal ions is a very sensitive hyperfine specroscopy technique called the perturbed angular correlation technique (PAC).

  15. High-energy metal ion implantation for reduction of surface resistivity of alumina ceramica)

    Science.gov (United States)

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

    2012-02-01

    In this work, the possibility to increase the surface conductivity of ceramic insulators through their treatment with accelerated metal ion beams produced by a MevvaV.Ru vacuum arc source is demonstrated. The increase in surface conductivity is made possible due to experimental conditions in which an insulated collector is charged by beam ions to a potential many times lower than the accelerating voltage, and hence, than the average beam ion energy. The observed effect of charge neutralization of the accelerated ion beam is presumably associated with electrons knocked out of the electrodes of the accelerating system of the source and of the walls of the vacuum chamber by the accelerated ions.

  16. Characteristics of flows of energetic atoms reflected from metal targets during ion bombardment

    Science.gov (United States)

    Kuzmichev, A.; Perevertaylo, V.; Tsybulsky, L.; Volpian, O.

    2016-07-01

    Particle number and energy reflection coefficients for energetic neutralized gas ions (Ar and O atoms) backscattered from metal targets during ion bombardment have been calculated using TRIM code. The energy distributions of reflected atoms are computed, too, and their dependence on the primary ion energy and the angle of ion incidence is determined. The obtained data confirm the possibility of employing energetic atoms reflection for generation of high energy neutral beams and point out to take this phenomenon into account under analysis of the ion technology for coating deposition.

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

    Science.gov (United States)

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

    2017-10-01

    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 with a mean age of 65 years at surgery were randomized to a MoM (Metasul) or a MoP (Protasul) bearing. After 16 years, 38 patients had died and 4 had undergone revision surgery. 13 patients were unavailable for clinical follow-up, leaving 30 patients (n = 14 MoM and n = 16 MoP) for analysis of metal ion concentrations and clinical outcome. Results - 15-year implant survival was similar in both groups (MoM 96% [95% CI 88-100] versus MoP 97% [95% CI 91-100]). The mean serum cobalt concentration was 4-fold higher in the MoM (1.5 μg/L) compared with the MoP cohort (0.4 μg/L, p MoM (2.2 μg/L) compared with the MoP cohort (1.0 μg/L, p = 0.05). Mean creatinine levels were similar in both groups (MoM 93 μmol/L versus MoP 92 μmol/L). Harris hip scores differed only marginally between the MoM and MoP cohorts. Interpretation - This is the longest follow-up of a randomized trial on 28-mm MoM articulations, and although implant survival in the 2 groups was similar, metal ion concentrations remained elevated in the MoM cohort even in the long term.

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

    African Journals Online (AJOL)

    carbodithioate and imidazole-1-carbodithioate were employed as sorbents for heavy metals from aqueous environments. The equilibrating time, initial metal concentrations and sorbent mass for optimal adsorption were 40 min, 5 mg/ℓ and 8 mg, ...

  19. Development of a 10 GHz “Multi-Mode” ECR, Ion Source for the Production of Multiply Charged Ions from Metallic Elements

    Science.gov (United States)

    Trassl, R.; Thompson, W. R.; Broetz, F.; Pawlowsky, M.; McCullough, R. W.; Salzborn, E.

    An all-permanent magnet ECR “multi-mode” ion source with emphasis on the production of metallic ions has been built. The main feature of this ion source is a stepped plasma chamber with a larger diameter in the resonance region in order to allow the propagation of higher microwave modes than the ground mode. Ions from metallic elements can be produced using both the insertion technique and an evaporation oven. First spectra obtained for Oxygen and Bismuth are shown.

  20. Improving Passivation Process of Si Nanocrystals Embedded in SiO2 Using Metal Ion Implantation

    Directory of Open Access Journals (Sweden)

    Jhovani Bornacelli

    2013-01-01

    Full Text Available We studied the photoluminescence (PL of Si nanocrystals (Si-NCs embedded in SiO2 obtained by ion implantation at MeV energy. The Si-NCs are formed at high depth (1-2 μm inside the SiO2 achieving a robust and better protected system. After metal ion implantation (Ag or Au, and a subsequent thermal annealing at 600°C under hydrogen-containing atmosphere, the PL signal exhibits a noticeable increase. The ion metal implantation was done at energies such that its distribution inside the silica does not overlap with the previously implanted Si ion . Under proper annealing Ag or Au nanoparticles (NPs could be nucleated, and the PL signal from Si-NCs could increase due to plasmonic interactions. However, the ion-metal-implantation-induced damage can enhance the amount of hydrogen, or nitrogen, that diffuses into the SiO2 matrix. As a result, the surface defects on Si-NCs can be better passivated, and consequently, the PL of the system is intensified. We have selected different atmospheres (air, H2/N2 and Ar to study the relevance of these annealing gases on the final PL from Si-NCs after metal ion implantation. Studies of PL and time-resolved PL indicate that passivation process of surface defects on Si-NCs is more effective when it is assisted by ion metal implantation.

  1. Metal ion release from silver soldering and laser welding caused by different types of mouthwash.

    Science.gov (United States)

    Erdogan, Ayse Tuygun; Nalbantgil, Didem; Ulkur, Feyza; Sahin, Fikrettin

    2015-07-01

    To compare metal ion release from samples welded with silver soldering and laser welding when immersed into mouthwashes with different ingredients. A total of 72 samples were prepared: 36 laser welded and 36 silver soldered. Four samples were chosen from each subgroup to study the morphologic changes on their surfaces via scanning electron microscopy (SEM). Each group was further divided into four groups where the samples were submerged into mouthwash containing sodium fluoride (NaF), mouthwash containing sodium fluoride + alcohol (NaF + alcohol), mouthwash containing chlorhexidine (CHX), or artificial saliva (AS) for 24 hours and removed thereafter. Subsequently, the metal ion release from the samples was measured with inductively coupled plasma mass spectrometry (ICP-MS). The metal ion release among the solutions and the welding methods were compared. The Kruskal-Wallis and analysis of variance (ANOVA) tests were used for the group comparisons, and post hoc Dunn multiple comparison test was utilized for the two group comparisons. The level of metal ion release from samples of silver soldering was higher than from samples of laser welding. Furthermore, greater amounts of nickel, chrome, and iron were released from silver soldering. With regard to the mouthwash solutions, the lowest amounts of metal ions were released in CHX, and the highest amounts of metal ions were released in NaF + alcohol. SEM images were in accord with these findings. The laser welding should be preferred over silver soldering. CHX can be recommended for patients who have welded appliances for orthodontic reasons.

  2. Biosorption of heavy metal ions from aqueous solution by red macroalgae.

    Science.gov (United States)

    Ibrahim, Wael M

    2011-09-15

    Biosorption is an effective process for the removal and recovery of heavy metal ions from aqueous solutions. The biomass of marine algae has been reported to have high biosorption capacities for a number of heavy metal ions. In this study, four species of red seaweeds Corallina mediterranea, Galaxaura oblongata, Jania rubens and Pterocladia capillacea were examined to remove Co(II), Cd(II), Cr(III) and Pb(II) ions from aqueous solution. The experimental parameters that affect the biosorption process such as pH, contact time and biomass dosage were studied. The maximum biosorption capacity of metal ions was 105.2mg/g at biomass dosage 10 g/L, pH 5 and contact time 60 min. The biosorption efficiency of algal biomass for the removal of heavy metal ions from industrial wastewater was evaluated for two successive cycles. Galaxaura oblongata biomass was relatively more efficient to remove metal ions with mean biosorption efficiency of 84%. This study demonstrated that these seaweeds constitute a promising, efficient, cheap and biodegradable sorbent biomaterial for lowering the heavy metal pollution in the environment. Copyright © 2011 Elsevier B.V. All rights reserved.

  3. Infrared Spectroscopy of Metal Ion Complexes: Models for Metal Ligand Interactions and Solvation

    Science.gov (United States)

    Duncan, Michael

    2006-03-01

    Weakly bound complexes of the form M^+-Lx (M=Fe, Ni, Co, etc.; L=CO2, C2H2, H2O, benzene, N2) are prepared in supersonic molecular beams by laser vaporization in a pulsed-nozzle cluster source. These species are mass analyzed and size-selected in a reflectron time-of-flight mass spectrometer. Clusters are photodissociated at infrared wavelengths with a Nd:YAG pumped infrared optical parametric oscillator/amplifier (OPO/OPA) laser or with a tunable infrared free-electron laser. M^+-(CO2)x complexes absorb near the free CO2 asymmetric stretch near 2349 cm-1 but with an interesting size dependent variation in the resonances. Small clusters have blue-shifted resonances, while larger complexes have additional bands due to surface CO2 molecules not attached to the metal. M^+(C2H2)n complexes absorb near the C-H stretches in acetylene, but resonances in metal complexes are red-shifted with repect to the isolated molecule. Ni^+ and Co^+ complexes with acetylene undergo intracluster cyclization reactions to form cyclobutadiene. Transition metal water complexes are studied in the O-H stretch region, and partial rotational structure can be measured. M^+(benzene) and M^+(benzene)2 ions (M=V, Ti, Al) represent half-sandwich and sandwich species, whose spectra are measured near the free benzene modes. These new IR spectra and their assignments will be discussed as well as other new IR spectra for similar complexes.

  4. Production of multicharged metal ion beams on the first stage of tandem-type ECRIS

    Energy Technology Data Exchange (ETDEWEB)

    Hagino, Shogo, E-mail: hagino@nf.eie.eng.osaka-u.ac.jp; Nagaya, Tomoki; Nishiokada, Takuya; Otsuka, Takuro; Sato, Fuminobu; Kato, Yushi [Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita-shi, Osaka 565-0871 (Japan); Muramatsu, Masayuki; Kitagawa, Atsushi [National Institute of Radiological Sciences (NIRS), 4-9-1, Anagawa, Inage-ku, Chiba-shi, Chiba 263-8555 (Japan)

    2016-02-15

    Multicharged metal ion beams are required to be applied in a wide range of fields. We aim at synthesizing iron-endohedral fullerene by transporting iron ion beams from the first stage into the fullerene plasma in the second stage of the tandem-type electron cyclotron resonance ion source (ECRIS). We developed new evaporators by using a direct ohmic heating method and a radiation heating method from solid state pure metal materials. We investigate their properties in the test chamber and produce iron ions on the first stage of the tandem-type ECRIS. As a result, we were successful in extracting Fe{sup +} ion beams from the first stage and introducing Fe{sup +} ion beams to the second stage. We will try synthesizing iron-endohedral fullerene on the tandem-type ECRIS by using these evaporators.

  5. Heavy ion time-of-flight ERDA of high dose metal implanted germanium

    Energy Technology Data Exchange (ETDEWEB)

    Dytlewski, N.; Evans, P.J.; Noorman, J.T. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia); Wielunski, L.S. [Commonwealth Scientific and Industrial Research Organisation (CSIRO), Lindfield, NSW (Australia). Div. of Applied Physics; Bunder, J. [New South Wales Univ., Wollongong, NSW (Australia). Wollongong Univ. Coll

    1996-12-31

    With the thick Ge substrates used in ion implantation, RBS can have difficulty in resolving the mass-depth ambiguities when analysing materials composed of mixtures of elements with nearly equal masses. Additional, and complimentary techniques are thus required. This paper reports the use of heavy ion time-of-flight elastic recoil detection analysis (ToF- ERDA), and conventional RBS in the analysis of Ge(100) implanted with high dose Ti and Cu ions from a MEWA ion source . Heavy ion ToF ERDA has been used to resolve, and profile the implanted transition metal species, and also to study any oxygen incorporation into the sample resulting from the implantation, or subsequential reactions with air or moisture. This work is part of a study on high dose metal ion implantation of medium atomic weight semiconductor materials. 13 refs., 6 figs.

  6. Recovery of metals from simulant spent lithium-ion battery as organophosphonate coordination polymers in aqueous media

    Energy Technology Data Exchange (ETDEWEB)

    Perez, Emilie; Andre, Marie-Laure; Navarro Amador, Ricardo [ICSM, Institut de Chimie Séparative de Marcoule, UMR 5257, CEA/CNRS/ENSCM/UM, Bât 426, BP 17171, 30207 Bagnols-sur-Cèze cedex (France); Hyvrard, François; Borrini, Julien [SARPI VEOLIA, Direction Technique et Innovations, Zone portuaire de Limay-Porcheville, 427 route du Hazay, 78520 Limay (France); Carboni, Michaël, E-mail: michael.carboni@cea.fr [ICSM, Institut de Chimie Séparative de Marcoule, UMR 5257, CEA/CNRS/ENSCM/UM, Bât 426, BP 17171, 30207 Bagnols-sur-Cèze cedex (France); Meyer, Daniel [ICSM, Institut de Chimie Séparative de Marcoule, UMR 5257, CEA/CNRS/ENSCM/UM, Bât 426, BP 17171, 30207 Bagnols-sur-Cèze cedex (France)

    2016-11-05

    Highlights: • Original waste disposal strategies for battery. • Precipitation of metals as coordination polymers. • Organo-phosphonate coordination polymers. • Selective extraction of manganese or co-precipitation of manganese/cobalt. • The recycling process give a promising application on any waste solution. - Abstract: An innovative approach is proposed for the recycling of metals from a simulant lithium-ion battery (LIBs) waste aqueous solution. Phosphonate organic linkers are introduced as precipitating agents to selectively react with the metals to form coordination polymers from an aqueous solution containing Ni, Mn and Co in a hydrothermal process. The supernatant is analyzed by ICP-AES to quantify the efficiency and the selectivity of the precipitation and the materials are characterized by Scanning Electron Microscopy (SEM), Powder X-Ray Diffraction (PXRD), Thermogravimetric Analyses (TGA) and nitrogen gas sorption (BET). Conditions have been achieved to selectively precipitate Manganese or Manganese/Cobalt from this solution with a high efficiency. This work describes a novel method to obtain potentially valuable coordination polymers from a waste metal solution that can be generalized on any waste solution.

  7. Effect of transition metal ions on the conductivity and stability of stabilized zirconia

    DEFF Research Database (Denmark)

    Lybye, D.; Mogensen, Mogens Bjerg

    2007-01-01

    Zirconia compounds stabilised with rare-earth metal oxides like yttria, ytterbia and scandia are known to be good oxide ion conductors suitable as electrolyte material in solid oxide fuel cells. However. stabilised zirconia with high oxide ion conductivity is often only metastable at fuel cell...

  8. Metal Cation Binding to Gas-Phase Pentaalanine: Divalent Ions Restructure the Complex

    NARCIS (Netherlands)

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

    2013-01-01

    Ion-neutral complexes of pentaalalanine with several singly- and doubly charged metal ions are examined using conformation analysis by infrared multiple photon dissociation (IRMPD) spectroscopy and density functional theory (DFT) computations. The infrared spectroscopy in the 1500-1800 cm(-1) region

  9. The effects of metal ion contaminants on the double stranded DNA helix and diseases.

    Science.gov (United States)

    Theophanides, T; Anastassopoulou, J

    2017-08-24

    Mineral metal ions are essential for the maintenance of the reactions that regulate homeostasis and the functions of our body. It is known that the regulation of the neurodegenerative system depends directly on life metal ions, such as Na, K, Mg, Ca, Fe, Mo, Cu, Co, Zn, Cr, Mn, while the toxic metals Cd, Pb, Hg, etc disturb homeostasis, leading to diseases. Particularly significant is the effect of toxic metals on the double stranded forms of DNA and conformations. It was found that the toxic metal ions by reacting specifically with the nucleic bases and electrostatically with the negatively phosphate groups of the DNA backbone cause changes in the structure of the DNA double helix, leading to breaks of single or double strands. Accumulation of these defects affects the protecting systems of the body and induces mutations, eventually leading to serious diseases. There are many metal ions, such as Cr, Al, Cd, Cu, Ni, which by binding directly to DNA molecule or by developing oxidative stress increase the instability of DNA, promoting epigenetic changes that lead to DNA damage. Toxic metal ions induce indirect DNA damage and influence the gene stability by inactivating encoding proteins or by changing the redox potential and the signaling of metalloenzymes.

  10. Enhanced highly charged ion production using a metal-dielectric liner in the KVI 14 GHz ECR ion source

    NARCIS (Netherlands)

    Schachter, L; Dobrescu, S; Rodrigues, G; Drentje, AG

    Forming on an aluminum surface a dielectric layer of alumina (aluminum oxide) in order to create a metal-dielectric (MD) structure increases the secondary-electron emission properties. The idea of using this material as a MD (Al-Al2O3) cylindrical liner inside an ECR ion source was previously tested

  11. Role of metal ion incorporation in ion exchange resin on the selectivity of fluoride

    Energy Technology Data Exchange (ETDEWEB)

    Viswanathan, Natrayasamy [Department of Chemistry, Gandhigram Rural University, Gandhigram 624302, Tamilnadu (India)], E-mail: natrayasamy_viswanathan@rediffmail.com; Meenakshi, S. [Department of Chemistry, Gandhigram Rural University, Gandhigram 624302, Tamilnadu (India)], E-mail: drs_meena@rediffmail.com

    2009-03-15

    Indion FR 10 resin has sulphonic acid functional group (H{sup +} form) possesses appreciable defluoridation capacity (DC) and its DC has been enhanced by chemical modification into Na{sup +} and Al{sup 3+} forms by loading respective metal ions in H{sup +} form of resin. The DCs of Na{sup +} and Al{sup 3+} forms were found to be 445 and 478 mg F{sup -}/kg, respectively, whereas the DC of H{sup +} form is 265 mg F{sup (}/kg at 10 mg/L initial fluoride concentration. The nature and morphology of sorbents are characterized using FTIR and SEM analysis. The fluoride sorption was explained using the Freundlich, Langmuir and Redlich-Peterson isotherms and kinetic models. The calculated thermodynamic parameters such as {delta}G{sup o}, {delta}H{sup o}, {delta}S{sup o} and sticking probability (S{sup *}) explains the nature of sorption. Comparison was also made by the elution capacity of these resins in order to select a cost effective material. A field trial was carried out to test the suitability of the resins with fluoride water collected from a nearby fluoride-endemic area.

  12. Selective fluorescence sensors for detection of nitroaniline and metal Ions based on ligand-based luminescent metal-organic frameworks

    Science.gov (United States)

    Yu, Zongchao; Wang, Fengqin; Lin, Xiangyi; Wang, Chengmiao; Fu, Yiyuan; Wang, Xiaojun; Zhao, Yongnan; Li, Guodong

    2015-12-01

    Metal-organic frameworks (MOFs) are porous crystalline materials with high potential for applications in fluorescence sensors. In this work, two solvent-induced Zn(II)-based metal-organic frameworks, Zn3L3(DMF)2 (1) and Zn3L3(DMA)2(H2O)3 (2) (L=4,4‧-stilbenedicarboxylic acid), were investigated as selective sensing materials for detection of nitroaromatic compounds and metal ions. The sensing experiments show that 1 and 2 both exhibit selective fluorescence quenching toward nitroaniline with a low detection limit. In addition, 1 exhibits high selectivity for detection of Fe3+ and Al3+ by significant fluorescence quenching or enhancement effect. While for 2, it only exhibits significant fluorescence quenching effect for Fe3+. The results indicate that 1 and 2 are both promising fluorescence sensors for detecting and recognizing nitroaniline and metal ions with high sensitivity and selectivity.

  13. Ion exchange during heavy metal bio-sorption from aqueous solution by dried biomass of macrophytes.

    Science.gov (United States)

    Verma, V K; Tewari, Saumyata; Rai, J P N

    2008-04-01

    In this study, potentials of oven dried biomass of Eichhornia crassipes, Valisneria spiralis and Pistia stratiotes, were examined in terms of their heavy metal (Cd, Ni, Zn, Cu, Cr and Pb) sorption capacity, from individual-metal and multi-metal aqueous solutions at pH 6.0+/-0.1 (a popular pH of industrial effluent). V. spiralis was the most and E. crassipes was the least efficient for removal of all the metals. Cd, Pb and Zn were efficiently removed by all the three biomass. Cd was removed up to 98% by V. spiralis. Sorption data for Cr, Ni and Cd fitted better to Langmuir isotherm equation, while, the sorption data for Pb, Zn and Cu fitted better to Freundlich isotherm equation. In general, the presence of other metal ions did not influence significantly the targeted metal sorption capacity of the test plant biomasses. Ion exchange was proven the main mechanism involved in bio-sorption and there was a strong ionic balance between adsorbed (H(+) and M(2+)) to the released ions (Na(+) and K(+)) to and from the biomass. No significant difference was observed in the metal exchanged amount, by doubling of metal concentration (15-30 mg/l) in the solution and employing individual-metal and multi-metal solutions.

  14. Effects of complexing compounds on sorption of metal ions to cement

    Energy Technology Data Exchange (ETDEWEB)

    Loevgren, Lars [Umeaa Univ. (Sweden). Inorganic chemistry

    2005-12-15

    This present report is a literature review addressing the effects of complexing ligands on the sorption of radionuclides to solid materials of importance for repositories of radioactive waste. Focus is put on laboratory studies of metal ion adsorption to cement in presence of chelating agents under strongly alkaline conditions. As background information, metal sorption to different mineral and cement phases in ligand free systems is described. Furthermore, surface complexation model (SCM) theories are introduced. According to surface complexation theories these interactions occur at specific binding sites at the particle/water interface. Adsorption of cationic metals is stronger at high pH, and the adsorption of anions occurs preferentially at low pH. The adsorption of ions to mineral surfaces is a result of both chemical bonding and electrostatic attraction between the ions and charged mineral surfaces. By combining uptake data with spectroscopic information the sorption can be explained on a molecular level by structurally sound surface complexation models. Most of the metal sorption studies reviewed are dealing with minerals exhibiting oxygen atoms at their surfaces, mainly oxides of Fe(II,III) and Al(III), and aluminosilicates. Investigations of radionuclides are focused on clay minerals, above all montmorillonite and illite. Which mechanism that is governing the metal ion adsorption to a given mineral is to a large extent depending on the metal adsorbed. For instance, sorption of Ni to montmorillonite can occur by formation of inner-sphere mononuclear surface complexes located at the edges of montmorillonite platelets and by formation of a Ni phyllosilicate phase parallel to montmorillonite layers. Also metal uptake to cement materials can occur by different mechanisms. Cationic metals can both be attached to cement (calcium silicate hydrate, CSH) and hardened cement paste (HCP) by formation of inner-sphere complexes at specific surface sites and by

  15. Label-free histamine detection with nanofluidic diodes through metal ion displacement mechanism.

    Science.gov (United States)

    Ali, Mubarak; Ramirez, Patricio; Duznovic, Ivana; Nasir, Saima; Mafe, Salvador; Ensinger, Wolfgang

    2017-02-01

    We design and characterize a nanofluidic device for the label-free specific detection of histamine neurotransmitter based on a metal ion displacement mechanism. The sensor consists of an asymmetric polymer nanopore fabricated via ion track-etching technique. The nanopore sensor surface having metal-nitrilotriacetic (NTA-Ni2+) chelates is obtained by covalent coupling of native carboxylic acid groups with Nα,Nα-bis(carboxymethyl)-l-lysine (BCML), followed by exposure to Ni2+ ion solution. The BCML immobilization and subsequent Ni2+ ion complexation with NTA moieties change the surface charge concentration, which has a significant impact on the current-voltage (I-V) curve after chemical modification of the nanopore. The sensing mechanism is based on the displacement of the metal ion from the NTA-Ni2+ chelates. When the modified pore is exposed to histamine solution, the Ni2+ ion in NTA-Ni2+ chelate recognizes histamine through a metal ion coordination displacement process and formation of stable Ni-histamine complexes, leading to the regeneration of metal-free NTA groups on the pore surface, as shown in the current-voltage characteristics. Nanomolar concentrations of the histamine in the working electrolyte can be detected. On the contrary, other neurotransmitters such as glycine, serotonin, gamma-aminobutyric acid, and dopamine do not provoke significant changes in the nanopore electronic signal due to their inability to displace the metal ion and form a stable complex with Ni2+ ion. The nanofluidic sensor exhibits high sensitivity, specificity and reusability towards histamine detection and can then be used to monitor the concentration of biological important neurotransmitters. Copyright © 2016 Elsevier B.V. All rights reserved.

  16. Poultry litter-based activated carbon for removing heavy metal ions in water.

    Science.gov (United States)

    Guo, Mingxin; Qiu, Guannan; Song, Weiping

    2010-02-01

    Utilization of poultry litter as a precursor material to manufacture activated carbon for treating heavy metal-contaminated water is a value-added strategy for recycling the organic waste. Batch adsorption experiments were conducted to investigate kinetics, isotherms, and capacity of poultry litter-based activated carbon for removing heavy metal ions in water. It was revealed that poultry litter-based activated carbon possessed significantly higher adsorption affinity and capacity for heavy metals than commercial activated carbons derived from bituminous coal and coconut shell. Adsorption of metal ions onto poultry litter-based carbon was rapid and followed Sigmoidal Chapman patterns as a function of contact time. Adsorption isotherms could be described by different models such as Langmuir and Freundlich equations, depending on the metal species and the coexistence of other metal ions. Potentially 404 mmol of Cu2+, 945 mmol of Pb2+, 236 mmol of Zn2+, and 250-300 mmol of Cd2+ would be adsorbed per kg of poultry litter-derived activated carbon. Releases of nutrients and metal ions from litter-derived carbon did not pose secondary water contamination risks. The study suggests that poultry litter can be utilized as a precursor material for economically manufacturing granular activated carbon that is to be used in wastewater treatment for removing heavy metals.

  17. Removal of toxic heavy metal ions in runoffs by modified alfalfa and juniper

    Science.gov (United States)

    J.S. Han; J.K. Park; S.H. Min

    2000-01-01

    A series of batch isotherm tests was performed with alfalfa and juniper fibers to evaluate the effectiveness in filtering toxic heavy metals from stormwater. The adsorption of the heavy metal ions on the alfalfa and juniper fibers was strongly dependent on the equilibrium pH value of the solution. The change in sorption rate over time showed that two different sorption...

  18. Sono-electrochemical recovery of metal ions from their aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Bingfeng; Fishgold, Asher [Department of Materials Science and Engineering, The University of Arizona, 1235 E. James E. Rogers Way, Tucson, AZ 85721 (United States); Lee, Paul [Department of Chemistry and Biochemistry, The University of Arizona, 1306 E. University Blvd, Tucson, AZ 85721 (United States); Runge, Keith; Deymier, Pierre [Department of Materials Science and Engineering, The University of Arizona, 1235 E. James E. Rogers Way, Tucson, AZ 85721 (United States); Keswani, Manish, E-mail: manishk@email.arizona.edu [Department of Materials Science and Engineering, The University of Arizona, 1235 E. James E. Rogers Way, Tucson, AZ 85721 (United States)

    2016-11-15

    Highlights: • Sono-electrochemical method is effective in the recovery of Pd, Ga and Pb. • Recovery efficiency depends on the type of metal ion and megasonic frequency used. • Pd is recovered mainly in metallic form while Ga and Pb show presence of oxide. - Abstract: Metal recovery from aqueous waste streams is an important goal for recycling, agriculture and mining industries. The development of more effective methods of recovery have been of increasing interest. The most common methods for metal recovery include precipitation, electrochemical, ion exchange, flocculation/coagulation and filtration. In the current work, a sono-electrochemical technique employing sound field at megasonic frequency (500 kHz or 1 MHz) in conjunction with electrochemistry is evaluated for enhanced recovery of selected metal ions (palladium, lead and gallium) with different redox potentials from their aqueous solutions. The surface morphology and elemental composition of the metal deposits were characterized using scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. The percent recovery was found to depend on the type of metal ion and the megasonic frequency used. Palladium was recovered in its metal form, while lead and gallium were oxidized during or after the recovery process.

  19. Platinum metals-solution chemistry and separation methods (ion-exchange and solvent extraction)

    Energy Technology Data Exchange (ETDEWEB)

    Al-Bazi, S.J.; Chow, A. (Manitoba Univ., Winnipeg (Canada). Dept. of Chemistry)

    1984-10-01

    The effects of knowledge of the solution chemistry of the platinum metals on their separation by solvent extraction and ion-exchange methods are reviewed, for the period 1950 to 1983. The review concentrates on the chloro-complexes of these metals and indicates those areas which need more investigation or interpretation to provide adequate separational methods.

  20. Examining metallic glass formation in LaCe:Nb by ion implantation

    Directory of Open Access Journals (Sweden)

    Sisson Richard

    2017-01-01

    Full Text Available In order to combine niobium (Nb with lanthanum (La and cerium (Ce, Nb ions were deposited within a thin film of these two elements. According to the Hume-Rothery rules, these elements cannot be combined into a traditional crystalline metallic solid. The creation of an amorphous metallic glass consisting of Nb, La, and Ce is then investigated. Amorphous metallic glasses are traditionally made using fast cooling of a solution of molten metals. In this paper, we show the results of an experiment carried out to form a metallic glass by implanting 9 MeV Nb 3+ atoms into a thin film of La and Ce. Prior to implantation, the ion volume distribution is calculated by Monte Carlo simulation using the SRIM tool suite. Using multiple methods of electron microscopy and material characterization, small quantities of amorphous metallic glass are indeed identified.

  1. A Typical Metal-Ion-Responsive Color-Tunable Emitting Insulated π-Conjugated Polymer Film.

    Science.gov (United States)

    Hosomi, Takuro; Masai, Hiroshi; Fujihara, Tetsuaki; Tsuji, Yasushi; Terao, Jun

    2016-10-17

    We report the synthesis of an insulated π-conjugated polymer containing 2,2'-bipyridine moieties as metal coordination sites. Metal coordination to the polymer enabled easy and reversible tuning of the luminescent color without changes to the main chain skeleton. The permethylated α-cyclodextrin (PM α-CD)-based insulation structure allowed the metalated polymers to demonstrate efficient emission even in the solid state, with identical spectral shapes to the dilute solutions. In addition, the coordination ability of the metal-free polymer was maintained in the solid state, resulting in reversible changes in the luminescent color in response to the metal ions. The synthesized polymer is expected to be suitable for application in recyclable luminescent sensors to distinguish different metal ions. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Generation of oxygen, carbon and metallic ion beams by a compact microwave source

    Energy Technology Data Exchange (ETDEWEB)

    Walther, S.R.; Leung, K.N.; Ehlers, K.W.; Kunkel, W.B.

    1986-07-01

    A small microwave ion source fabricated from a quartz tube and enclosed externally by a cavity has been operated with different geometries and for various gases in a cw mode. This source has been used to generate oxygen ion beams with energy as low as 5.5 eV. Beam energy spread has been measured to be less than 1 eV. By installing different metal plates on the front extraction electrode, metallic ion beams such as (Be, Cu, Al, etc.) can be produced.

  3. Photoinduced charge accumulation by metal ion-coupled electron transfer.

    Science.gov (United States)

    Bonn, Annabell G; Wenger, Oliver S

    2015-10-07

    An oligotriarylamine (OTA) unit, a Ru(bpy)3(2+) photosensitizer moiety (Ru), and an anthraquinone (AQ) entity were combined to a molecular dyad (Ru-OTA) and a molecular triad (AQ-Ru-OTA). Pulsed laser excitation at 532 nm led to the formation of charge-separated states of the type Ru(-)-OTA(+) and AQ(-)-Ru-OTA(+) with lifetimes of ≤10 ns and 2.4 μs, respectively, in de-aerated CH3CN at 25 °C. Upon addition of Sc(OTf)3, very long-lived photoproducts were observed. Under steady-state irradiation conditions using a flux of (6.74 ± 0.21) × 10(15) photons per second at 450 nm, the formation of twofold oxidized oligotriarylamine (OTA(2+)) was detected in aerated CH3CN containing 0.02 M Sc(3+), as demonstrated unambiguously by comparison with UV-Vis absorption spectra obtained in the course of chemical oxidation with Cu(2+). Photodriven charge accumulation on the OTA unit of Ru-OTA and AQ-Ru-OTA is possible due to the lowering of the O2 reduction potential caused by the interaction of superoxide with the strong Lewis acid Sc(3+). The presence of the anthraquinone unit in AQ-Ru-OTA accelerates the rate-determining reaction step for charge accumulation by a factor of 10 compared to the Ru-OTA dyad. This is attributed to the formation of Sc(3+)-stabilized anthraquinone radical anion intermediates in the triad. Possible mechanistic pathways leading to charge accumulation are discussed. Photodriven charge accumulation is of key importance for solar fuels because their production will have to rely on multi-electron chemistry rather than single-electron reaction steps. Our study is the first to demonstrate that metal ion-coupled electron transfer (MCET) can be exploited to accumulate charges on a given molecular unit using visible light as an energy input. The approach of using a combination of intra- and intermolecular electron transfer reactions which are enabled by MCET is conceptually novel, and the fundamental insights gained from our study are relevant in the greater

  4. Transport of Alkali Metal Ions through a Liquid Membrane System ...

    African Journals Online (AJOL)

    crown-6, [K(MF18C6)](picrate) was determined by X-ray crystallography and showed that each potassium ion is eight-coordinate; each K+ ion is coordinated to the six oxygen atoms of the crown, to the phenolate oxygen atom and to one of the ...

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

    Indian Academy of Sciences (India)

    Home; Journals; Bulletin of Materials Science; Volume 34; Issue 1. Effect of ion beam ... Keywords. Composite materials; ion beam irradiation; dielectric properties; X-ray diffraction. ... Different concentrations (10, 20 and 40%) of Ni powder were dispersed in PMMA and the composite films were prepared by casting method.

  6. Removal of Heavy Metal Ions from Polluted Waters by Using of Low Cost Adsorbents: Review

    Directory of Open Access Journals (Sweden)

    M. Ghaedi

    2013-06-01

    Full Text Available Adsorption is a fundamental process in the physicochemical treatment of wastewaters which industries employ to reduce hazardous organic and inorganic wastes in effluents. In recent years the use of low-cost adsorbents has been widely investigated as a replacement for the currently costly methods of removing heavy metal ions from wastewater. It is well-known that cellulosic waste materials can be obtained and employed as cheap adsorbents and their performance to remove heavy metal ions can be affected upon chemical treatment. In this study, the use of some of low cost adsorbents for the removal of heavy metals from wastewater has been reviewed.

  7. Synthesis, Characterization and Metal Ion Detection of Novel Fluoroionophores Based on Heterocyclic Substituted Alanines

    Directory of Open Access Journals (Sweden)

    M. Manuela M Raposo

    2007-10-01

    Full Text Available The synthesis of new fluorescent probes containing the thiophene andbenzoxazole moieties combined with an alanine residue is described. The resulting highlyfluorescent heterocyclic alanine derivatives respond via a quenching effect, withparamagnetic Cu(II and Ni(II metal ions and with diamagnetic Hg(II, as shown by theabsorption and steady-state fluorescence spectroscopy studies. The formation ofmononuclear or dinuclear metal complexes was postulated based on the presence of thefree carboxylic acid as binding site and also with the interaction with the donor atoms inthe chromophore. Interaction with other important biological metal ions such as Zn(II,Ca(II and Na(I was also explored.

  8. Fluorescent nanoprobes for sensing and imaging of metal ions: recent advances and future perspectives.

    Science.gov (United States)

    Zhang, JingJing; Cheng, FangFang; Li, JingJing; Zhu, Jun-Jie; Lu, Yi

    2016-06-01

    Recent advances in nanoscale science and technology have generated nanomaterials with unique optical properties. Over the past decade, numerous fluorescent nanoprobes have been developed for highly sensitive and selective sensing and imaging of metal ions, both in vitro and in vivo. In this review, we provide an overview of the recent development of the design and optical properties of the different classes of fluorescent nanoprobes based on noble metal nanomaterials, upconversion nanoparticles, semiconductor quantum dots, and carbon-based nanomaterials. We further detail their application in the detection and quantification of metal ions for environmental monitoring, food safety, medical diagnostics, as well as their use in biomedical imaging in living cells and animals.

  9. Heavy metal ions in wines: meta-analysis of target hazard quotients reveal health risks

    Directory of Open Access Journals (Sweden)

    Petróczi Andrea

    2008-10-01

    Full Text Available Abstract Background Metal ions such as iron and copper are among the key nutrients that must be provided by dietary sources. Numerous foodstuffs have been evaluated for their contributions to the recommended daily allowance both to guide for satisfactory intake and also to prevent over exposure. In the case of heavy metal ions, the focus is often on exposure to potentially toxic levels of ions such as lead and mercury. The aim of this study is to determine target hazard quotients (THQ from literature reports giving empirical levels of metal ions in table wines using the reference upper safe limit value. Contributions to the THQ value were calculated for seven metal ions along with total values for each wine. Results The THQ values were determined as ranges from previously reported ranges of metal ion concentrations and were frequently concerningly high. Apart from the wines selected from Italy, Brazil and Argentina, all other wines exhibited THQ values significantly greater than one indicating levels of risk. The levels of vanadium, copper and manganese had the highest impact on THQ measures. Typical potential maximum THQ values ranged from 50 to 200 with Hungarian and Slovakian wines reaching 300. THQ values for a sample of red and white wines were high for both having values ranging from 30 to 80 for females based on a 250 mL glass per day. Conclusion The THQ values calculated are concerning in that they are mainly above the safe level of THQ

  10. Adaptation of intertidal biofilm communities is driven by metal ion and oxidative stresses

    KAUST Repository

    Zhang, Weipeng

    2013-11-11

    Marine organisms in intertidal zones are subjected to periodical fluctuations and wave activities. To understand how microbes in intertidal biofilms adapt to the stresses, the microbial metagenomes of biofilms from intertidal and subtidal zones were compared. The genes responsible for resistance to metal ion and oxidative stresses were enriched in both 6-day and 12-day intertidal biofilms, including genes associated with secondary metabolism, inorganic ion transport and metabolism, signal transduction and extracellular polymeric substance metabolism. In addition, these genes were more enriched in 12-day than 6-day intertidal biofilms. We hypothesize that a complex signaling network is used for stress tolerance and propose a model illustrating the relationships between these functions and environmental metal ion concentrations and oxidative stresses. These findings show that bacteria use diverse mechanisms to adapt to intertidal zones and indicate that the community structures of intertidal biofilms are modulated by metal ion and oxidative stresses.

  11. 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.

  12. Recent Progress in Graphite Intercalation Compounds for Rechargeable Metal (Li, Na, K, Al)-Ion Batteries.

    Science.gov (United States)

    Xu, Jiantie; Dou, Yuhai; Wei, Zengxi; Ma, Jianmin; Deng, Yonghong; Li, Yutao; Liu, Huakun; Dou, Shixue

    2017-10-01

    Lithium-ion batteries (LIBs) with higher energy density are very necessary to meet the increasing demand for devices with better performance. With the commercial success of lithiated graphite, other graphite intercalation compounds (GICs) have also been intensively reported, not only for LIBs, but also for other metal (Na, K, Al) ion batteries. In this Progress Report, we briefly review the application of GICs as anodes and cathodes in metal (Li, Na, K, Al) ion batteries. After a brief introduction on the development history of GICs, the electrochemistry of cationic GICs and anionic GICs is summarized. We further briefly summarize the use of cationic GICs and anionic GICs in alkali ion batteries and the use of anionic GICs in aluminium-ion batteries. Finally, we reach some conclusions on the drawbacks, major progress, emerging challenges, and some perspectives on the development of GICs for metal (Li, Na, K, Al) ion batteries. Further development of GICs for metal (Li, Na, K, Al) ion batteries is not only a strong supplement to the commercialized success of lithiated-graphite for LIBs, but also an effective strategy to develop diverse high-energy batteries for stationary energy storage in the future.

  13. Highly ordered three-dimensional macroporous carbon spheres for determination of heavy metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yuxiao; Zhang, Jianming [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China); Liu, Yang, E-mail: yangl@suda.edu.cn [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China); Huang, Hui [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China); Kang, Zhenhui, E-mail: zhkang@suda.edu.cn [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China)

    2012-04-15

    Highlights: Black-Right-Pointing-Pointer Highly ordered three dimensional macroporous carbon spheres (MPCSs) were prepared. Black-Right-Pointing-Pointer MPCS was covalently modified by cysteine (MPCS-CO-Cys). Black-Right-Pointing-Pointer MPCS-CO-Cys was first time used in electrochemical detection of heavy metal ions. Black-Right-Pointing-Pointer Heavy metal ions such as Pb{sup 2+} and Cd{sup 2+} can be simultaneously determined. -- Abstract: An effective voltammetric method for detection of trace heavy metal ions using chemically modified highly ordered three dimensional macroporous carbon spheres electrode surfaces is described. The highly ordered three dimensional macroporous carbon spheres were prepared by carbonization of glucose in silica crystal bead template, followed by removal of the template. The highly ordered three dimensional macroporous carbon spheres were covalently modified by cysteine, an amino acid with high affinities towards some heavy metals. The materials were characterized by physical adsorption of nitrogen, scanning electron microscopy, and transmission electron microscopy techniques. While the Fourier-transform infrared spectroscopy was used to characterize the functional groups on the surface of carbon spheres. High sensitivity was exhibited when this material was used in electrochemical detection (square wave anodic stripping voltammetry) of heavy metal ions due to the porous structure. And the potential application for simultaneous detection of heavy metal ions was also investigated.

  14. Synthesis and kinetics of growth of metal nanoparticles inside ion-exchange polymers

    Energy Technology Data Exchange (ETDEWEB)

    Zolotukhina, Ekaterina V., E-mail: ks-chem@mail.r [Voronezh State University of Technology, Moskovsky pr., 14, Voronezh 394026 (Russian Federation); Kravchenko, Tamara A. [Voronezh State University, Universitetskaya pl., 1, Voronezh 394006 (Russian Federation)

    2011-04-01

    Copper and silver nanoparticles have been obtained by means of saturation of a sulfostyrene-divinylbenzene cation-exchange polymer with metal ions and their subsequent chemical reduction. This procedure was repeated several times up to formation of a long-range conducting network (percolating cluster). Another system under study was an ensemble of Ag nanoparticles of various sizes on the silver electrode surface obtained by reduction of anodically formed layers of silver oxide. Recrystallization of deposited metal crystals inside the polymer matrix in contact with metal-ion containing solution is very slow for electrically separated particles. Formation of the electric network results in an enormous acceleration of this process via electron-ion mechanism, with growth of the average particle size, so that their potential will approach that of the compact metal with time. The initial period of the particle growth is well described by the parabolic law (Burke and Turnbull). The values of the particle-growth coefficient in this law, k, are drastically different for particles inside the matrix and on the electrode surface. Particle-to-particle electron transfer is impeded by insulating areas inside the polymer matrix. Besides, ionogenic centers of the matrix restrict the mobility of metal cations, thus slowing down the ion transfer within the recrystallization circuit. These observations have allowed us to establish the conditions resulting in long-term stabilization of metal nanoparticles inside the ion-exchange matrix with respect to their recrystallization.

  15. 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 coefficients. It is found that proper modeling of these solutions requires the inclusion of electronic polarization of the 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

  16. Designing antimicrobial bioactive glass materials with embedded metal ions synthesized by the sol–gel method

    Energy Technology Data Exchange (ETDEWEB)

    Palza, Humberto, E-mail: hpalza@ing.uchile.cl [Departamento de Ingeniería Química y Biotecnología, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Santiago (Chile); Escobar, Blanca; Bejarano, Julian [Departamento de Ingeniería Química y Biotecnología, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Santiago (Chile); Bravo, Denisse [Departamento de Patología, Facultad de Odontología, Universidad de Chile, Santiago (Chile); Diaz-Dosque, Mario [Departamento de Ciencias Básicas y Comunitarias, Facultad de Odontología, Universidad de Chile, Santiago (Chile); Perez, Javier [Departamento de Ingeniería Química y Biotecnología, Facultad de Ciencias Físicas y Matemáticas, Universidad de Chile, Santiago (Chile)

    2013-10-15

    Bioactive glasses (SiO{sub 2}–P{sub 2}O{sub 5}–CaO) having tailored concentrations of different biocide metal ions (copper or silver) were produced by the sol–gel method. All the particles release phosphorous ions when immersed in water and simulated body fluid (SBF). Moreover, a surface layer of polycrystalline hydroxy-carbonate apatite was formed on the particle surfaces after 10 day immersion in SBF as confirmed by X-ray diffraction and scanning electron microscopy (SEM) showing the bioactive materials. Samples with embedded either copper or silver ions were able to further release the biocide ions with a release rate that depends on the metal embedded and the dissolution medium: water or SBF. This biocide ion release from the samples explains the antimicrobial effect of our active particles against Escherichia coli DH5α ampicillin-resistant (Gram-negative) and Streptococcus mutans (Gram-positive) as determined by the Minimum Bactericidal Concentration (MBC) method. The antimicrobial behavior of the particles depends on the bacteria and the biocide ion used. Noteworthy, although samples with copper are able to release more metal ion than samples with silver, they present higher MBC showing the high effect of silver against these bacteria. - Highlights: • Copper and silver act as antimicrobial additives in bioactive glass materials. • Silver is more toxic than copper ions in these bioactive materials. • Sol–gel method allows the synthesis of antimicrobial bioactive materials.

  17. Hydration number of alkali metal ions determined by insertion in a conducting polymer

    DEFF Research Database (Denmark)

    Skaarup, Steen

    2008-01-01

    of all other water molecules whose properties are still influenced significantly by the cation. Knowing the hydration number is important when considering, for instance, the transport of Na+ and K+ in biological cell membranes, since their different behavior may depend on the details of ion hydration....... 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...... direct calculation of the number of M+ ions entering the film, and therefore the inserted M+ mass. The mass of the water molecules is calculated as a difference. The results yield the following primary hydration numbers: Li+: 5.5-5.6; Na+: 4.0-4.1; K+: 2.0-2.5; Rb+: 0.6-1.2; Cs+: ~0. The most important...

  18. A flexible zwitterion ligand based lanthanide metal-organic framework for luminescence sensing of metal ions and small molecules.

    Science.gov (United States)

    Wen, Rong-Mei; Han, Song-De; Ren, Guo-Jian; Chang, Ze; Li, Yun-Wu; Bu, Xian-He

    2015-06-28

    A new lanthanide metal-organic framework was constructed using a tripodal flexible zwitterion ligand (H3LBr3) which takes a chair-shaped configuration. The luminescence of the compound displays highly selective sensing of the Fe(3+) ion and nitrobenzene.

  19. Kinetics of metal ion binding by polysaccharide colloids

    NARCIS (Netherlands)

    Rotureau, E.; Leeuwen, van H.P.

    2008-01-01

    The dynamics of metal sorption by a gel-like polysaccharide is investigated by means of the electrochemical technique of stripping chronopotentiometry (SCP). The measured response reflects the diffusive flux properties of the metallic species in the dispersion. The colloidal ligand studied here is a

  20. Removal of some metal ions from aqueous solution using orange ...

    African Journals Online (AJOL)

    STORAGESEVER

    2008-09-03

    Sep 3, 2008 ... 1Department of Pure and Industrial Chemistry, University of Port Harcourt, P.M.B. 5323, Port Harcourt, Rivers State,. Nigeria. 2 Department ... removal of heavy metals from contaminated soil and waste water. A number of technologies have been deve- loped over the years to remove toxic metals from water.

  1. New polymer-supported ion-complexing agents: design, preparation and metal ion affinities of immobilized ligands.

    Science.gov (United States)

    Alexandratos, Spiro D

    2007-01-31

    Polymer-supported reagents are comprised of crosslinked polymer networks that have been modified with ligands capable of selective metal ion complexation. Applications of these polymers are in environmental remediation, ion chromatography, sensor technology, and hydrometallurgy. Bifunctional polymers with diphosphonate/sulfonate ligands have a high selectivity for actinide ions. The distribution coefficient for the uranyl ion from 1 M nitric acid is 70,000, compared to 900 for the monophosphonate/sulfonate polymer and 200 for the sulfonic acid ion-exchange resin. A bifunctional trihexyl/triethylammonium polymer has a high affinity and selectivity for pertechnetate and perchlorate anions from groundwater. In one example, its distribution coefficient for perchlorate ions in the presence of competing anions is 3,300,000, compared to 203,180 for a commercially available anion-exchange resin. Polystyrene modified with N-methyl-D-glucamine ligands is capable of selectively complexing arsenate from groundwater. It complexes 99% of the arsenate present in a solution of 100 mg/L arsenate with 560 mg/L sulfate ions. Its selectivity is retained even in the presence of 400 mg/L phosphate. There is no affinity for arsenate above pH 9, allowing for the polymer to be regenerated with moderate alkali solution. In studies aimed at developing a Hg(II)-selective resin, simple amine resins were found to have a high Hg(II) affinity and that affinity is dependent upon the solution pH and the counterion.

  2. Metallic Sn-Based Anode Materials: Application in High-Performance Lithium-Ion and Sodium-Ion Batteries.

    Science.gov (United States)

    Ying, Hangjun; Han, Wei-Qiang

    2017-11-01

    With the fast-growing demand for green and safe energy sources, rechargeable ion batteries have gradually occupied the major current market of energy storage devices due to their advantages of high capacities, long cycling life, superior rate ability, and so on. Metallic Sn-based anodes are perceived as one of the most promising alternatives to the conventional graphite anode and have attracted great attention due to the high theoretical capacities of Sn in both lithium-ion batteries (LIBs) (994 mA h g-1) and sodium-ion batteries (847 mA h g-1). Though Sony has used Sn-Co-C nanocomposites as its commercial LIB anodes, to develop even better batteries using metallic Sn-based anodes there are still two main obstacles that must be overcome: poor cycling stability and low coulombic efficiency. In this review, the latest and most outstanding developments in metallic Sn-based anodes for LIBs and SIBs are summarized. And it covers the modification strategies including size control, alloying, and structure design to effectually improve the electrochemical properties. The superiorities and limitations are analyzed and discussed, aiming to provide an in-depth understanding of the theoretical works and practical developments of metallic Sn-based anode materials.

  3. Kinetics of metal ion binding by polysaccharide colloids.

    Science.gov (United States)

    Rotureau, Elise; van Leeuwen, Herman P

    2008-08-07

    The dynamics of metal sorption by a gel-like polysaccharide is investigated by means of the electrochemical technique of stripping chronopotentiometry (SCP). The measured response reflects the diffusive flux properties of the metallic species in the dispersion. The colloidal ligand studied here is a functionalized carboxymethyldextran. Its complexation with Pb(II) reveals a time dependence that identifies strong differences in the dynamic nature of the successive metal complexes formed. Apparently, the formation of intramolecular bidentate complexes requires a slow conformational reorganization of the macromolecule that becomes the rate-limiting step in the complexation reaction. The relevant parameters for metal binding and release kinetics are computed and thus provide knowledge of the time-dependent stability and lability of metal polysaccharide complexes.

  4. Multidiagnostic analysis of ion dynamics in ultrafast laser ablation of metals over a large fluence range

    Energy Technology Data Exchange (ETDEWEB)

    Anoop, K. K., E-mail: anoop.kiliyanamkandy@unina.it; Bruzzese, R.; Amoruso, S. [CNR-SPIN and Dipartimento di Fisica, Universita degli Studi di Napoli Federico II, Complesso Universitario Monte S. Angelo, Via Cintia, Napoli 80126 (Italy); Polek, M. P. [Center for Materials Under Extreme Environment, School of Nuclear Engineering, Purdue University, West Lafayette, Indiana 47907 (United States); Harilal, S. S. [Pacific Northwest National Laboratory, P.O. Box 999, Richland, Washington 99352 (United States)

    2015-02-28

    The dynamics of ions in ultrafast laser ablation of metals is studied over fluences ranging from the ablation threshold up to ≈75 J/cm{sup 2} by means of three well-established diagnostic techniques. Langmuir probe, Faraday cup, and spectrally resolved intensified charge coupled device imaging simultaneously monitored the ions produced during ultrafast laser ablation of a pure copper target with 800 nm, ≈50 fs, Ti: Sapphire laser pulses. The fluence dependence of ion yield is analyzed, resulting in the observance of three different regimes. The specific ion yield shows a maximum at about 4–5 J/cm{sup 2}, followed by a gradual reduction and a transition to a high-fluence regime above ≈50 J/cm{sup 2}. The fluence dependence of the copper ions angular distribution is also analyzed, observing a gradual increase in forward-peaking of Cu ions for fluences up to ≈10 J/cm{sup 2}. A broader ion component is observed at larger angles for fluences larger than ≈10 J/cm{sup 2}. Finally, an experimental characterization of the ionic angular distribution for several metallic targets (Mg, Al, Cr, Fe, Cu, and W) is carried out at a relatively high fluence of ≈66 J/cm{sup 2}. Interestingly, the ion emission from the volatile metals shows a narrow, forward-peaked distribution, and a high peak ion yield compared to the refractory metals. Moreover, the width of ionic angular distributions presents a striking correlation with the peak ion yield.

  5. DFT study of the interaction between DOTA chelator and competitive alkali metal ions.

    Science.gov (United States)

    Frimpong, E; Skelton, A A; Honarparvar, B

    2017-09-01

    1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetracetic acid (DOTA) is an important chelator for radiolabeling of pharmaceuticals. The ability of alkali metals found in the body to complex with DOTA and compete with radio metal ions can alter the radiolabeling process. Non-covalent interactions between DOTA complexed with alkali metals Li + , Na + , K + and Rb + , are investigated with density functional theory using B3LYP and ωB97XD functionals. Conformational possibilities of DOTA were explored with a varying number of carboxylic pendant arms of DOTA in close proximity to the ions. It is found that the case in which four arms of DOTA are interacting with ions is more stable than other conformations. The objective of this study is to explore the electronic structure properties upon complexation of alkali metals Li + Na + , K + and Rb + with a DOTA chelator. Interaction energies, relaxation energies, entropies, Gibbs free energies and enthalpies show that the stability of DOTA, complexed with alkali metals decreases down the group of the periodic table. Implicit water solvation affects the complexation of DOTA-ions leading to decreases in the stability of the complexes. NBO analysis through the natural population charges and the second order perturbation theory, revealed a charge transfer between DOTA and alkali metals. Conceptual DFT-based properties such as HOMO/LUMO energies, ΔE HOMO-LUMO and chemical hardness and softness indicated a decrease in the chemical stability of DOTA-alkali metal complexes down the alkali metal series. This study serves as a guide to researchers in the field of organometallic chelators, particularly, radiopharmaceuticals in finding the efficient optimal match between chelators and various metal ions. Copyright © 2017 Elsevier Inc. All rights reserved.

  6. Selective fluorescence sensors for detection of nitroaniline and metal Ions based on ligand-based luminescent metal-organic frameworks

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Zongchao [College of Environment and Chemical Engineering & Key Lab of Hollow Fiber Membrane Materials & Membrane Process, Tianjin Polytechnic University, Tianjin 300387 (China); Wang, Fengqin, E-mail: wangfengqin@tjpu.edu.cn [College of Environment and Chemical Engineering & Key Lab of Hollow Fiber Membrane Materials & Membrane Process, Tianjin Polytechnic University, Tianjin 300387 (China); Lin, Xiangyi [Suzhou Huihe Pharmaceutical Limited Company, Suzhou 215200 (China); Wang, Chengmiao; Fu, Yiyuan; Wang, Xiaojun [College of Environment and Chemical Engineering & Key Lab of Hollow Fiber Membrane Materials & Membrane Process, Tianjin Polytechnic University, Tianjin 300387 (China); Zhao, Yongnan [College of Materials and Engineering & Key Lab of Hollow Fiber Membrane Materials & Membrane Process, Tianjin Polytechnic University, Tianjin 300387 (China); Li, Guodong [The State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130023 (China)

    2015-12-15

    Metal-organic frameworks (MOFs) are porous crystalline materials with high potential for applications in fluorescence sensors. In this work, two solvent-induced Zn(II)–based metal-organic frameworks, Zn{sub 3}L{sub 3}(DMF){sub 2} (1) and Zn{sub 3}L{sub 3}(DMA){sub 2}(H{sub 2}O){sub 3} (2) (L=4,4′-stilbenedicarboxylic acid), were investigated as selective sensing materials for detection of nitroaromatic compounds and metal ions. The sensing experiments show that 1 and 2 both exhibit selective fluorescence quenching toward nitroaniline with a low detection limit. In addition, 1 exhibits high selectivity for detection of Fe{sup 3+} and Al{sup 3+} by significant fluorescence quenching or enhancement effect. While for 2, it only exhibits significant fluorescence quenching effect for Fe{sup 3+}. The results indicate that 1 and 2 are both promising fluorescence sensors for detecting and recognizing nitroaniline and metal ions with high sensitivity and selectivity. - Graphical abstract: Two MOFs have been selected as the fluorescence sensing materials for selectively sensing mitroaromatic compounds and metal ions. The high selectivity makes them promising fluorescence sensors for detecting and recognizing nitroaniline and Fe{sup 3+} or Al{sup 3+}.

  7. Supercharging with Trivalent Metal Ions in Native Mass Spectrometry

    Science.gov (United States)

    Flick, Tawnya G.; Williams, Evan R.

    2012-11-01

    Addition of 1.0 mM LaCl3 to aqueous ammonium acetate solutions containing proteins in their folded native forms can result in a significant increase in the molecular ion charging obtained with electrospray ionization as a result of cation adduction. In combination with m-nitrobenzyl alcohol, molecular ion charge states that are greater than the number of basic sites in the protein can be produced from these native solutions, even for lysozyme, which is conformationally constrained by four intramolecular disulfide bonds. Circular dichroism spectroscopy indicates that the conformation of ubiquitin is not measurably affected with up to 1.0 M LaCl3, but ion mobility data indicate that the high charge states that are formed when 1.0 mM LaCl3 is present are more unfolded than the low charge states formed without this reagent. These and other results indicate that the increased charging is a result of La3+ preferentially adducting onto compact or more native-like conformers during ESI and the gas-phase ions subsequently unfolding as a result of increased Coulomb repulsion. Electron capture dissociation of these high charge-state ions formed from these native solutions results in comparable sequence coverage to that obtained for ions formed from denaturing solutions without supercharging reagents, making this method a potentially powerful tool for obtaining structural information in native mass spectrometry.

  8. Hydrometallurgical process for the recovery of metal values from spent lithium-ion batteries in citric acid media.

    Science.gov (United States)

    Chen, Xiangping; Zhou, Tao

    2014-11-01

    In this paper, a hydrometallurgical process has been proposed to recover valuable metals from spent lithium-ion batteries in citric acid media. Leaching efficiencies as high as 97%, 95%, 94%, and 99% of Ni, Co, Mn, and Li were achieved under the optimal leaching experimental conditions of citric acid concentration of 2 mol L(-1), leaching temperature of 80 °C, leaching time of 90 min, liquid-solid ratio of 30 ml g(-1), and 2 vol. % H2O2. For the metals recovery process, nickel and cobalt were selectively precipitated by dimethylglyoxime reagent and ammonium oxalate sequentially. Then manganese was extracted by Na-D2EHPA and the manganese-loaded D2EHPA was stripped with sulfuric acid. The manganese was recovered as MnSO4 in aqueous phase and D2EHPA could be reused after saponification. Finally, lithium was precipitated by 0.5 mol L(-1) sodium phosphate. Under their optimal conditions, the recovery percentages of Ni, Co, Mn, and Li can reach 98%, 97%, 98%, and 89%, respectively. This is a relatively simple route in which all metal values could be effectively leached and recovered in citric acid media. © The Author(s) 2014.

  9. Physicochemical studies on Ciclopirox olamine complexes with divalent metal ions.

    Science.gov (United States)

    Tarawneh, Ruba T; Hamdan, Imad I; Bani-Jaber, Ahmad; Darwish, Rula M

    2005-01-31

    Ciclopirox olamine (CPO) metal complexes have been prepared and characterized using elemental analysis, infra red (IR), melting point and differential scanning calorimetry (DSC). Spectroscopic titration using molar ratio method indicated the occurrence of 1:1 complexes for CPO with almost all the examined metals. Physicochemical properties were also studied including aqueous solubility and apparent partition coefficient. Results showed that generally complex formation dramatically decreased the solubility and increased apparent partition coefficient. However, some metal complexes exhibited opposite effect. It could be concluded that complex formation can modify the solubility and apparent partition coefficient, which may suggest the use of complexes to manipulate the physicochemical properties of the drug.

  10. 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.

  11. Removal of some metal ions by activated carbon prepared from Phaseolus aureus hulls

    Energy Technology Data Exchange (ETDEWEB)

    Rao, M. Madhava; Ramana, D.K.; Seshaiah, K. [Analytical and Environmental Chemistry Division, Department of Chemistry, Sri Venkateswara University, Tirupati 517 502 (India); Wang, M.C., E-mail: mcwang@cyut.edu.tw [Department of Environmental Engineering and Management, Chaoyang University of Technology, Wufong Township 41349, Taichung County, Taiwan (China); Chien, S.W. Chang [Department of Environmental Engineering and Management, Chaoyang University of Technology, Wufong Township 41349, Taichung County, Taiwan (China)

    2009-07-30

    Removal of lead [Pb(II)], zinc [Zn(II)], copper [Cu(II)], and cadmium [Cd(II)] from aqueous solutions using activated carbon prepared from Phaseolus aureus hulls (ACPAH), an agricultural waste was studied. The influence of various parameters such as effect of pH, contact time, adsorbent dose, and initial concentration of metal ions on the removal was evaluated by batch method. The removal of metal ions by ACPAH was pH dependent and the optimum pH values were 7.0, 8.0, 7.0 and 6.0 for Cu(II), Cd(II), Zn(II), and Pb(II), respectively. The sorption isotherms were studied using Langmuir, Freundlich, Dubinin-Radushkevich (D-R), and Temkin isotherm models. The maximum adsorption capacity values of ACPAH for metal ions were 21.8 mg g{sup -1} for Pb(II), 21.2 mg g{sup -1} for Zn(II), 19.5 mg g{sup -1} for Cu(II), and 15.7 mg g{sup -1} for Cd(II). The experiments demonstrated that the removal of metal ions followed the pseudo-second-order kinetic model. Desorption experiments were carried out using HCl solution with a view to regenerate the spent adsorbent and to recover the adsorbed metal ions.

  12. A mononuclear non-heme manganese(IV)-oxo complex binding redox-inactive metal ions.

    Science.gov (United States)

    Chen, Junying; Lee, Yong-Min; Davis, Katherine M; Wu, Xiujuan; Seo, Mi Sook; Cho, Kyung-Bin; Yoon, Heejung; Park, Young Jun; Fukuzumi, Shunichi; Pushkar, Yulia N; Nam, Wonwoo

    2013-05-01

    Redox-inactive metal ions play pivotal roles in regulating the reactivities of high-valent metal-oxo species in a variety of enzymatic and chemical reactions. A mononuclear non-heme Mn(IV)-oxo complex bearing a pentadentate N5 ligand has been synthesized and used in the synthesis of a Mn(IV)-oxo complex binding scandium ions. The Mn(IV)-oxo complexes were characterized with various spectroscopic methods. The reactivities of the Mn(IV)-oxo complex are markedly influenced by binding of Sc(3+) ions in oxidation reactions, such as a ~2200-fold increase in the rate of oxidation of thioanisole (i.e., oxygen atom transfer) but a ~180-fold decrease in the rate of C-H bond activation of 1,4-cyclohexadiene (i.e., hydrogen atom transfer). The present results provide the first example of a non-heme Mn(IV)-oxo complex binding redox-inactive metal ions that shows a contrasting effect of the redox-inactive metal ions on the reactivities of metal-oxo species in the oxygen atom transfer and hydrogen atom transfer reactions.

  13. Metal Ions-Stimulated Iron Oxidation in Hydroxylases Facilitates Stabilization of HIF-1α Protein

    Science.gov (United States)

    Kaczmarek, Monika; Cachau, Raul E.; Topol, Igor A.; Kasprzak, Kazimierz S.; Ghio, Andy; Salnikow, Konstantin

    2009-01-01

    The exposure of cells to several metal ions stabilizes HIF-1α protein. However, the molecular mechanisms are not completely understood. They may involve inhibition of hydroxylation by either substitution of iron by metal ions or by iron oxidation in the hydroxylases. Here we provide evidence supporting the latter mechanism. We show that HIF-1α stabilization in human lung epithelial cells occurred following exposure to various metal and metalloid ions, including those that cannot substitute for iron in the hydroxylases. In each case addition of the reducing agent ascorbic acid (AA)* abolished HIF-1α protein stabilization. To better understand the role of iron oxidation in hydroxylase inhibition and to define the role of AA in the enzyme recovery we applied molecular modeling techniques. Our results indicate that the energy required for iron substitution by Ni(II) in the enzyme is high and unlikely to be achieved in a biological system. Additionally, computer modeling allowed us to identify a tridentate coordination of AA with the enzyme-bound iron, which explains the specific demand for AA as the iron reductant. Thus, the stabilization of HIF-1α by numerous metal ions that cannot substitute for iron in the enzyme, the alleviation of this effect by AA, and our computer modeling data support the hypothesis of iron oxidation in the hydroxylases following exposure to metal ions. PMID:19074761

  14. Effect Of Metal Ions On Triphenylmethane Dye Decolorization By Laccase From Trametes Versicolor

    Directory of Open Access Journals (Sweden)

    Chmelová Daniela

    2015-12-01

    Full Text Available The aim of this study was investigate the influence of different metal ions on laccase activity and triphenylmethane dye decolorization by laccase from white-rot fungus Trametes versicolor. Laccase activity was inhibited by monovalent ions (Li+, Na+, K+ and Ag+ but the presence of divalent ions increased laccase activity at the concentration of 10 mmol/l. The effect of metal ions on decolorization of triphenylmethane dyes with different structures namely Bromochlorophenol Blue, Bromophenol Blue, Bromocresol Blue and Phenol Red was tested. The presence of metal ions (Na+, K+, Mg2+, Ca2+, Ba2+, Mn2+, Zn2+ slightly decreased triphenylmethane dye decolorization by laccase from T. versicolor except Na+ and Mg2+, which caused the increase of decolorization for all tested dyes. Decolorization of selected dyes showed that the presence of low-molecular-weight compounds is necessary for effective decolorization. Hydroxybenzotriazole (HBT is the most frequently used. Although HBT belongs to most frequently used redox mediator and generally increase decolorization efficiency, so its presence decreased decolorization percentage of Bromophenol Blue and Bromochlorophenol Blue, the influence of metal ions to dye decolorization by laccase has the similar course with or without presence of redox mediator HBT.

  15. Influence of metal ions intercalation on the vibrational dynamics of water confined between MXene layers

    Science.gov (United States)

    Osti, Naresh C.; Naguib, Michael; Ganeshan, Karthik; Shin, Yun K.; Ostadhossein, Alireza; van Duin, Adri C. T.; Cheng, Yongqiang; Daemen, Luke L.; Gogotsi, Yury; Mamontov, Eugene; Kolesnikov, Alexander I.

    2017-11-01

    Two-dimensional (2D) carbides and nitrides of early transition metals (MXenes) combine high conductivity with hydrophilic surfaces, which make them promising for energy storage, electrocatalysis, and water desalination. The effects of intercalated metal ions on the vibrational states of water confined in Ti3C2Tx MXenes have been explored using inelastic neutron scattering (INS) and molecular-dynamics simulations to better understand the mechanisms that control MXenes' behavior in aqueous electrolytes, water purification, and other important applications. We observe an INS signal from water in all samples, pristine and with lithium, sodium, or potassium ions intercalated between the 2D Ti3C2Tx layers. However, only a small amount of water is found to reside in Ti3C2Tx intercalated with metal ions. Water in pristine Ti3C2Tx is more disordered, with bulklike characteristics, in contrast to intercalated Ti3C2Tx , where water is more ordered, irrespective of the metal ions used for intercalation. The ordering of the confined water increases with the ion size. This finding is further confirmed from molecular-dynamics simulation, which showed an increase in interference of water molecules with increasing ion size resulting in a concomitant decrease in water mobility, therefore providing guidance to tailor MXene properties for energy and environmental applications.

  16. Determination of metal ion content of beverages and estimation of target hazard quotients: a comparative study

    Directory of Open Access Journals (Sweden)

    Barker James

    2008-06-01

    Full Text Available Abstract Background Considerable research has been directed towards the roles of metal ions in nutrition with metal ion toxicity attracting particular attention. The aim of this study is to measure the levels of metal ions found in selected beverages (red wine, stout and apple juice and to determine their potential detrimental effects via calculation of the Target Hazard Quotients (THQ for 250 mL daily consumption. Results The levels (mean ± SEM and diversity of metals determined by ICP-MS were highest for red wine samples (30 metals totalling 5620.54 ± 123.86 ppb followed by apple juice (15 metals totalling 1339.87 ± 10.84 ppb and stout (14 metals totalling 464.85 ± 46.74 ppb. The combined THQ values were determined based upon levels of V, Cr, Mn, Ni, Cu, Zn and Pb which gave red wine samples the highest value (5100.96 ± 118.93 ppb followed by apple juice (666.44 ± 7.67 ppb and stout (328.41 ± 42.36 ppb. The THQ values were as follows: apple juice (male 3.11, female 3.87, stout (male 1.84, female 2.19, red wine (male 126.52, female 157.22 and ultra-filtered red wine (male 110.48, female 137.29. Conclusion This study reports relatively high levels of metal ions in red wine, which give a very high THQ value suggesting potential hazardous exposure over a lifetime for those who consume at least 250 mL daily. In addition to the known hazardous metals (e.g. Pb, many metals (e.g. Rb have not had their biological effects systematically investigated and hence the impact of sustained ingestion is not known.

  17. Adsorption of heavy metal ions onto dithizone-anchored poly (EGDMA-HEMA) microbeads.

    Science.gov (United States)

    Salih, B; Denizli, A; Kavaklı, C; Say, R; Pişkin, E

    1998-08-01

    The dithizone-anchored poly (EGDMA-HEMA) microbeads were prepared for the removal of heavy metal ions (i.e. cadmium, mercury, chromium and lead) from aqueous media containing different amounts of these ions (25-500 ppm) and at different pH values (2.0-8.0). The maximum adsorptions of heavy metal ions onto the dithizone-anchored microbeads from their solutions was 18.3, Cd(II); 43.1, Hg(II); 62.2, Cr(III) and 155.2 mg g(-1) for Pb(II). Competition between heavy metal ions (in the case of adsorption from mixture) yielded adsorption capacities of 9.7, Cd(II); 28.7, Hg(II); 17.6, Cr(III) and 38.3 mg g(-1) for Pb(II). The same affinity order was observed under non-competitive and competitive adsorption, i.e. Cr(III)>Pb(II)>Hg(II)>Cd(II). The adsorption of heavy metal ions increased with increasing pH and reached a plateaue value at around pH 5.0. Heavy metal ion adsorption from artificial wastewater was also studied. The adsorption capacities are 4.3, Cd(II); 13.2, Hg(II); 7.2, Cr(III) and 16.4 mg g(-1) for Pb(II). Desorption of heavy metal ions was achieved using 0.1 M HNO(3). The dithizone-anchored microbeads are suitable for repeated use (for more than five cycles) without noticeable loss of capacity.

  18. Development of dithizone based fibre optic evanescent wave sensor for heavy metal ion detection in aqueous environments

    Science.gov (United States)

    Bhavsar, K.; Prabhu, R.; Pollard, P.

    2013-06-01

    Detection of highly toxic heavy metal ions requires rapid, simple, sensitive and selective detection methods in the environment. Optical fibre based sensing facilitates the remote, continuous and in-situ detection approaches in the environment. Herein, we report the development of a dithizone based fibre optic sensor with a simple procedure to detect heavy metal ions in the aqueous environment using an evanescent wave sensing approach. The chromogenic ligand dithizone and its spectral specificity with metal ions has been elaborated in this work.

  19. Method for intercalating alkali metal ions into carbon electrodes

    Science.gov (United States)

    Doeff, Marca M.; Ma, Yanping; Visco, Steven J.; DeJonghe, Lutgard

    1995-01-01

    A low cost, relatively flexible, carbon electrode for use in a secondary battery is described. A method is provided for producing same, including intercalating alkali metal salts such as sodium and lithium into carbon.

  20. Constructed molecular sensor to enhance metal detection by bacterial ribosomal switch-ion channel protein interaction.

    Science.gov (United States)

    Cuero, Raul; Lilly, J; McKay, David S

    2012-03-31

    Molecular biosensors are useful tools that detect metal ions or other potentially toxic chemicals. However, the efficiency of conventional sensors is limited in mixed metals substrates, which is the common way they are found in nature. The use of biosensors constructed from genetically modified living microbial systems has the potential of providing sensitive detection systems for specific toxic targets. Consequently, our investigation was aimed at assembling different genetic building blocks to produce a focused microbial biosensor with the ability to detect specific metals. This objective was achieved by using a synthetic biology approach. Our genetic building blocks, including a synchronized ribosomal switch-iron ion channel, along with sequences of promoters, metal-binding proteins (Fe, Pb), ribosomal binding sites, yellow fluorescence reporter protein (YFRP), and terminators, were constructed within the same biobrick in Escherichia coli. We used an rpoS ribosomal switch containing an aptamer, which responds to the specific metal ligands, in synchronization with an iron ion channel, TonB. This switch significantly stimulates translation, as expressed by higher fluorescence, number of colonies, and concentration of RNA in E. coli. The positive results show the effectiveness of using genetically tailored synchronized ribosomal switch-ion channels to construct microbial biosensors to detect specific metals, as tested in iron solutions. Copyright © 2012 Elsevier B.V. All rights reserved.

  1. Some features of ion mixing during simultaneous ion implantation and deposition of metallic coatings

    CERN Document Server

    Pogrebnyak, A D; Mikhalev, A D; Shablya, V T; Yanovskij, V P

    2001-01-01

    The results on the Ta, Cu ions implantation into the aluminium substrate by simultaneous deposition of these ions in the form of coatings are presented. The complex structure of these coatings from the given elements in the substrate, as well as the increase in the microhardness, adhesion and corrosion resistance growth are determined. It is shown on the basis of the results of the secondary ions energy distribution, that intermetallic phases are formed in the substrate surface layer

  2. Computational study of the effective three-ion interaction potentials in liquid metals with high density of electron gas

    OpenAIRE

    Vasiliu, E. V.

    2002-01-01

    Based on the many-body theory of metals in the third order of the perturbation expansion in electron-ion interaction pseudopotential, the potentials of pair and three-ion interactions are calculated in liquid lead, aluminium and beryllium at their melting temperatures. The reducible and irreducible three-ion interactions have an attractive nature on distances approximately equal to an average distance between ions in metals. It results in the shortening of average interatomic distance in an e...

  3. Direct trace analysis of metals and alloys in a quadrupole ion-trap mass spectrometer

    CERN Document Server

    Song, K S; Yang, M; Cha, H K; Lee, J M; Lee, G H

    1999-01-01

    An ion-trap mass spectrometer adopting a quadrupole ion-trap and laser ablation/ionization method was constructed. The developed system was tested for composition analysis of some metals (Cu, stainless), and alloys (hastalloy C, mumetal) by mass spectrometry. Samples were analyzed by using laser ablation from a sample probe tip followed by a mass analysis with the quadrupole ion-trap. The quadrupole ion-trap was modified to enable laser ablation by a XeCl excimer laser pulse that passed radially through the ring electrode. A mass scan of the produced ions was performed in the mass selective instability mode wherein trapped ions were successively detected by increasing the rf voltage through the ring electrode. Factors affecting the mass resolution, such as pressure of buffer gas and ablation laser power, are discussed.

  4. Fluorescent metal ion indicators based on benzoannelated crown systems: a green fluorescent indicator for intracellular sodium ions.

    Science.gov (United States)

    Martin, Vladimir V; Rothe, Anca; Gee, Kyle R

    2005-04-01

    The synthesis and metal binding properties of cation-sensitive fluorescent indicators intended for biological applications are described. The increase of the crown ether ring size enhances the affinity for larger cations, but weakens the fluorescent response and selectivity. A compound having a 15-crown-5 chelator directly attached to a 2,7-difluoroxanthenone fluorophore loads into live cells and responds to sodium ion concentration changes with large fluorescence increases in the visible wavelength range.

  5. 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.

  6. Environmental effects on the structure of metal ion-DOTA complexes: An ab initio study of radiopharmaceutical metals.

    Energy Technology Data Exchange (ETDEWEB)

    Lau, E Y; Lightstone, F C; Colvin, M E

    2006-02-10

    Quantum mechanical calculations were performed to study the differences between the important radiopharmaceutical metals yttrium (Y) and indium (In) bound by DOTA and modified DOTA molecules. Energies were calculated at the MP2/6-31+G(d)//HF/6-31G(d) levels, using effective core potentials on the Y and In ions. Although the minimum energy structures obtained are similar for both metal ion-DOTA complexes, changes in coordination and local environment significantly affect the geometries and energies of these complexes. Coordination by a single water molecule causes a change in the coordination number and a change in the position of the metal ion in In-DOTA; but, Y-DOTA is hardly affected by water coordination. When one of the DOTA carboxylates is replaced by an amide, the coordination energy for the amide arm shows a large variation between the Y and In ions. Optimizations including water and guandinium moieties to approximate the effects of antibody binding indicate a large energy cost for the DOTA-chelated In to adopt the ideal conformation for antibody binding.

  7. Asymptomatic prospective and retrospective cohorts with metal-on-metal hip arthroplasty indicate acquired lymphocyte reactivity varies with metal ion levels on a group basis

    Science.gov (United States)

    Hallab, NJ; Caicedo, M; McAllister, K; Skipor, A; Amstutz, H; Jacobs, JJ

    2012-01-01

    Some tissues from metal-on-metal (MoM) hip arthroplasty revisions have shown evidence of adaptive-immune reactivity (i.e., excessive peri-implant lymphocyte infiltration/activation). We hypothesized that, prior to symptoms, some people with MoM hip arthroplasty will develop quantifiable metal-induced lymphocyte reactivity responses related to peripheral metal ion levels. We tested 3 cohorts (Group-1: n=21 prospective longitudinal MoM hip arthroplasty; Group-2: n=17 retrospective MoM hip arthroplasty; and Group-3: n=20 controls without implants). We compared implant position, metal-ion release, and immuno-reactivity. MoM cohorts had elevated (p2), compared with 76% of Group-2 and 15% of Group-3 controls (patch testing was a poor diagnostic indicator with only 1/21 Group-1 positive). Higher cup-abduction angles (50° vs. 40°) in Group-1 were associated with higher serum Cr (p<0.07). However, sub-optimal cup-anteversion angles (9° vs. 20°) had higher serum Co (p<0.08). Serum Cr and Co were significantly elevated in reactive vs. non-reactive Group-1 participants (p<0.04). CD4+CD69+ T-helper lymphocytes (but not CD8+) and IL-1β, IL-12 and IL-6 cytokines were all significantly elevated in metal-reactive vs. non-reactive Group-1 participants. Our results showed that lymphocyte reactivity to metals can develop within the first 1 to 4 years after MoM arthroplasty in asymptomatic patients and lags increases in metal ion levels. This increased metal reactivity was more prevalent in those individuals with extreme cup angles and higher amounts of circulating metal. PMID:22941579

  8. A Selective Bioreduction of Toxic Heavy Metal Ions from Aquatic Environment by Saccharomyces cerevisiae

    Directory of Open Access Journals (Sweden)

    A. M. Rahatgaonkar

    2008-01-01

    Full Text Available The need to remove or recover metal ions from industrial wastewater has been established in financial as well as environmental terms. This need has been proved financially in terms of cost saving through metal reuse or sale and environmentally as heavy metal toxicity can affect organisms throughout the food chain, including humans. Bioremediation of heavy metal pollution remains a major challenge in environmental biotechnology. Current removal strategies are mainly based on bioreduction of Co++, Ni++, Cu++ and Cd++ to their metallic forms by Saccharomyces cerevisiae in buffered aqueous solution. The rate of biotransformation was significantly influenced by pH of aqueous solution, concentration of biomass and hardness of water. All reaction conditions were optimized and maximum reduction of Co++, Cd++, Ni++ and Cu++ were observed as 80%, 63%, 50%, and 44% respectively. Unreacted Co++, Cd++, Ni++metal ions were extracted by 8-hydroxyquinoline and Cu++ by diethylthio carbamate in CHCl3 at different pH. Furthermore, the concentrations of unreacted metal ions were established spectrophotometrically.

  9. Serum Metal Ion Concentrations in Paediatric Patients following Total Knee Arthroplasty Using Megaprostheses

    Directory of Open Access Journals (Sweden)

    Jörg Friesenbichler

    2014-01-01

    Full Text Available The purpose of this study was to determine the concentrations of cobalt, chromium, and molybdenum in the serum of paediatric tumour patients after fixed hinge total knee arthroplasty. Further, these metal ion levels were compared with serum metal ion levels of patients with other orthopaedic devices such as hip and knee prostheses with metal-on-metal or metal-on-polyethylene articulation to find differences between anatomical locations, abrasion characteristics, and bearing surfaces. After an average follow-up of 108 months (range: 67 to 163 of 11 paediatric patients with fixed hinge total knee arthroplasty, the mean concentrations for Co and Cr were significantly increased while Mo was within the limits compared to the upper values from the reference laboratory. Furthermore, these serum concentrations were significantly higher compared to patients with a standard rotating hinge device (P=0.002 and P<0.001 and preoperative controls (P<0.001. On the other hand, the serum levels of patients following MoM THA or rotating hinge arthroplasty using megaprostheses were higher. Therefore, periodic long-term follow-ups are recommended due to the rising concerns about systemic metal ion exposure in the literature. Upon the occurrence of adverse reactions to metal debris the revision of the fixed hinge implant should be considered.

  10. Metallic borophene polytypes as lightweight anode materials for non-lithium-ion batteries.

    Science.gov (United States)

    Xiang, Pan; Chen, Xianfei; Zhang, Wentao; Li, Junfeng; Xiao, Beibei; Li, Longshan; Deng, Kuisen

    2017-09-20

    Applications of rechargeable non-lithium-ion batteries (Na + , K + , Ca 2+ , Mg 2+ , and Al 3+ NLIBs) are significantly hampered by the deficiency of suitable electrode materials. Searching for anode materials with desirable electrochemical performance is urgent for the large-scale energy storage demands of next generation renewable energy technologies. In this study, three types of recently synthesized borophenes are predicted to serve as high-performing anodes for NLIBs based on density functional theory. All the borophenes considered here are metallic with favorable in-plane stiffness. Dirac fermions were identified in two types of borophenes, guaranteeing their high electron mobility. Moreover, borophene configuration-dependent metal-ion migration, theoretical capacities, and open-circuit voltages were demonstrated with respect to the different adsorption behaviors and atom mass densities of anode materials. Our results provide insights into the configuration-dependent electrode performance of borophene and the corresponding metal-ion storage mechanism.

  11. Design dopamine-modified polypropylene fibers towards removal of heavy metal ions from water

    Directory of Open Access Journals (Sweden)

    K. Liu

    2017-04-01

    Full Text Available A simple approach to preparing dopamine-modified polypropylene fibers with a controllable polydopamine amount is supplied. By the dopamine modification, the hydrophobic polypropylene fibers have been changed into hydrophilic. The hydrophilicity can be improved by increasing the amount of polydopamine, as revealed by the contact angle evolutions. The hydrophilic dopamine-modified polypropylene fibers can rapidly and effectively remove copper and lead ions in water. Moreover, the performance of removing heavy metals is prominently improved as the polydopamine amount increases. This is because the polydopamine introduction can supply many available sites for adsorbing heavy metal ions, as revealed by theoretical simulation results. These results are crucial in future engineering fiber filters towards efficiently removing heavy metal ions using dopamine-modified polypropylene fibers.

  12. Design dopamine-modified polypropylene fibers towards removal of heavy metal ions from water

    Science.gov (United States)

    Liu, K.; Zhou, N. Y.; Xie, C. X.; Mou, B.; Ai, Y. N.

    2017-04-01

    A simple approach to preparing dopamine-modified polypropylene fibers with a controllable polydopamine amount is supplied. By the dopamine modification, the hydrophobic polypropylene fibers have been changed into hydrophilic. The hydrophilicity can be improved by increasing the amount of polydopamine, as revealed by the contact angle evolutions. The hydrophilic dopamine-modified polypropylene fibers can rapidly and effectively remove copper and lead ions in water. Moreover, the performance of removing heavy metals is prominently improved as the polydopamine amount increases. This is because the polydopamine introduction can supply many available sites for adsorbing heavy metal ions, as revealed by theoretical simulation results. These results are crucial in future engineering fiber filters towards efficiently removing heavy metal ions using dopamine-modified polypropylene fibers.

  13. Effects of impregnated metal ions on air/CO2-gasification of woody biomass.

    Science.gov (United States)

    Hurley, Scott; Li, Hanning; Xu, Chunbao Charles

    2010-12-01

    Several impregnated metal ions (Fe (III), Co (II), Ni (II), and Ru (IV)) and a raw iron ore (natural limonite) were examined as catalysts for gasification of pine sawdust in air/CO(2) at 700 and 800 degrees C. The yields of char and tar both increased with increasing CO(2) content in the feed gas. All the impregnated metal ions, in particular Ni (II), Co (II) and Ru (IV), were very effective for promoting biomass gasification in CO(2), leading to greatly reduced yields of tar and char accompanied by significantly enhanced formation of CO and H(2). At 800 degrees C, the impregnation of Fe (III), Ni (II), Co (II) or Ru (IV) led to almost complete conversion of the solid biomass into gas/liquid products, producing an extremely low char yield (tar yield reduced from 32.1 wt.% without catalyst to 19-27 wt.% with the impregnated metal ions. 2010 Elsevier Ltd. All rights reserved.

  14. Bio-functionalized silver nanoparticles for selective colorimetric sensing of toxic metal ions and antimicrobial studies

    Science.gov (United States)

    Vinod Kumar, V.; Anbarasan, S.; Christena, Lawrence Rene; SaiSubramanian, Nagarajan; Philip Anthony, Savarimuthu

    2014-08-01

    Hibiscus Sabdariffa (Gongura) plant extracts (leaves (HL) and stem (HS) were used for the first time in the green synthesis of bio-functionalized silver nanoparticles (AgNPs). The bio-functionality of AgNPs has been successfully utilized for selective colorimetric sensing of potentially health and environmentally hazardous Hg2+, Cd2+ and Pb2+ metal ions at ppm level in aqueous solution. Importantly, clearly distinguishable colour for all three metal ions was observed. The influence of extract preparation condition and pH were also explored on the formation of AgNPs. Both selectivity and sensitivity differed for AgNPs synthesized from different parts of the plant. Direct correlation between the stability of green synthesized AgNPs at different pH and its antibacterial effects has been established. The selective colorimetric sensing of toxic metal ions and antimicrobial effect of green synthesized AgNPs demonstrated the multifunctional applications of green nanotechnology.

  15. Malic enzyme: Tritium isotope effects with alternative dinucleotide substrates and divalent metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Karsten, W.E.; Harris, B.G.; Cook, P.F. (Texas College of Osteopathic Medicine, Fort Worth (United States))

    1992-01-01

    The NAD-malic enzyme from Ascaris suum catalyzes the divalent metal ion dependent oxidative decarboxylation of L-malate to yield pyruvate, carbon dioxide and NADH. Multiple isotope effect studies suggest a stepwise chemical mechanism with hydride transfer from L-malate to NAD occurring first to form oxalacetate, followed by decarboxylation. Utilizing L-malate-2-T, tritium V/K isotope effects have been determined for the hydride transfer step using a variety of alternative dinucleotide substrates and divalent metal ions. Combination of these data with deuterium isotope effects data and previously determined [sup 13]C isotope effects has allowed the calculation of intrinsic isotope effects for the malic enzyme catalyzed reaction. The identity of both the dinucleotide substrate and divalent metal ion has an effect of the size of the intrinsic isotope effect for hydride transfer.

  16. Shot-to-shot reproducibility in the emission of fast highly charged metal ions from a laser ion source.

    Science.gov (United States)

    Krása, J; Velyhan, A; Margarone, D; Krouský, E; Krouský, L; Jungwirth, K; Rohlena, K; Ullschmied, J; Parys, P; Ryć, L; Wołowski, J

    2012-02-01

    The generation of fast highly charged metal ions with the use of the sub-nanosecond Prague Asterix Laser System, operated at a fundamental wavelength of 1315 nm, is reported. Particular attention is paid to shot-to-shot reproducibility in the ion emission. Au and Pd targets were exposed to intensities up to 5 × 10(16) W∕cm(2). Above the laser intensity threshold of ∼3 × 10(14) W∕cm(2) the plasma is generated in a form of irregular bursts. The maximum energy of protons constituting the leading edge of the fastest burst reaches a value up to 1 MeV. The fast ions in the following bursts have energy gradually decreasing with the increasing burst number, namely, from a value of about 0.5 MeV∕charge regardless of the atomic number and mass of the ionized species.

  17. Off-line production of transition-metal ions at BECOLA

    Science.gov (United States)

    Ryder, Caleb; Asberry, Hillary; Harris, Justin; Mantica, Paul; Minamisono, Kei; Rossi, Dominic; Strum, Ryan; Smith, April

    2014-09-01

    Collinear laser spectroscopy (CLS) of stable reference beams produced using off-line methods is critical in CLS experiments for calibrating the beam energy during experimental runs, developing atomic laser excitation schemes and reliably deducing nuclear properties from hyperfine spectra collected from on-line beams of radioisotopes. The BEam COoler and LAser Spectroscopy (BECOLA) facility at the National Superconducting Cyclotron Laboratory at Michigan State University employs several ion sources for off-line stable beam production, each specializing in ion generation from specific materials. The focus of this talk will be on the Penning Ionization Gauge (PIG) ion source, a plasma sputtering source that has been recently implemented at BECOLA to readily produce transition metal ion beams. Collinear laser spectroscopy (CLS) of stable reference beams produced using off-line methods is critical in CLS experiments for calibrating the beam energy during experimental runs, developing atomic laser excitation schemes and reliably deducing nuclear properties from hyperfine spectra collected from on-line beams of radioisotopes. The BEam COoler and LAser Spectroscopy (BECOLA) facility at the National Superconducting Cyclotron Laboratory at Michigan State University employs several ion sources for off-line stable beam production, each specializing in ion generation from specific materials. The focus of this talk will be on the Penning Ionization Gauge (PIG) ion source, a plasma sputtering source that has been recently implemented at BECOLA to readily produce transition metal ion beams. This work was supported in part by NSF Grant No. PHY-11-02511.

  18. [Fluorescent labeling of latent fingerprints with metallic ions modified ZnS/PAMAM nano-composites].

    Science.gov (United States)

    Jin, Yu-Juan; Duan, Xiao-Bo; Lin, Yu-Meng; Wang, Si-Kun

    2013-03-01

    Abstract Effects of metallic ions, such as Zn2+ , Mn , Cd2+, Na+, K+, Ag, CuZ+ and PbZ, on the photoluminescence properties of ZnS(ZINC sulfide) QDs (quantum dots)/poly (amido amine) (PAMAM) dendrimer nanocomposites(NCs) with blue emission under the irradiation of UV light were studied. The results show that the effects of different metallic ions on the photoluminescence properties of the prepared ZnS QDs were different. Zn+ , Mn2+ and Cd2+ ions enhance the PL(photoluminescence) intensity; Na+ and K+ ions don't change the PL intensity obviously while Ag+, Cu2+ and Pb2+ quench it. Compared with ZnS/PAMAM NCs, fingerprints treated with ZnxCd1-x) S/PAMAM NCs emitted brighter blue light, the contrast between abstracts and fingerprints was more obvious, which shows good reference

  19. Optical and magnetic properties of transition-metal ions in tetrahedral and octahedral compounds

    Science.gov (United States)

    Li, Huifang; Wang, Huaiqian; Kuang, Xiaoyu

    2011-10-01

    This paper presents the complete energy matrix of the 3d2 system containing the electron-electron interaction, the ligand-field interaction, the spin-orbit coupling interaction, and the Zeeman interaction, in which the optical spectra and g-factor of V3+and Ti2+ ions in the series of tetrahedral AIIBVI (AII=Zn, Cd, BVI=S, Se, Te) semiconductor materials are determined. In the investigation of the optical and magnetic properties of these transition-metal ions in the tetrahedral coordination complexes, we compared the data obtained from the transition-metal ions in the tetrahedral coordination complexes with those obtained from the corresponding ions in the octahedral ones, and found that the tetrahedral complexes have weaker crystal-field strength, inverse energy level ordering and stronger covalence effect.

  20. Determination of membrane hydration numbers of alkali metal ions by insertion in a conducting polymer

    DEFF Research Database (Denmark)

    Skaarup, Steen; Junaid Mohamed Jafeen, Mohamed; Careem, M.A.

    2010-01-01

    , and a secondary (or outer) solvation shell, consisting of all other water molecules whose properties are still influenced significantly by the cation. Knowing the hydration number is important when considering, for instance, the transport of Na+ and K+ in biological cell membranes, since their different behavior...... may depend on the details of ion hydration. Although the solvation of alkali metal ions in aqueous solution has been discussed for many years, there is still no clear consensus. Part of the discrepancy is simply that different methods measure over different time scales, and therefore do...... not necessarily define the same hydration shell. This work presents a systematic study of one special variant 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-). The technique...

  1. Study on the adsorption of heavy metal ions from aqueous solution on modified SBA-15

    Directory of Open Access Journals (Sweden)

    Liliana Giraldo

    2013-01-01

    Full Text Available Amino-functionalized SBA-15 mesoporous silica was prepared, characterized, and used as an adsorbent for heavy metal ions. The organic - inorganic hybrid material was obtained by a grafting procedure using SBA-15 silica with 3-aminopropyl-triethoxysilane and bis(2,4,4-trimethylpentyl phosphinic acid (Cyanex 272, respectively. The structure and physicochemical properties of the materials were characterized by means of elemental analysis, X-ray diffraction (XRD, nitrogen adsorption - desorption, thermogravimetric analysis, FTIR spectroscopy and immersion calorimetry. The organic functional groups were successfully grafted onto the SBA-15 surface and the ordering of the support was not affected by the chemical modification. The behavior of the grafted solids was investigated for the adsorption of heavy metal ions from aqueous solutions. The hybrid materials showed high adsorption capacity and high selectivity for zinc ions. Other ions, such as cooper and cobalt were absorbed by the modified SBA-15 material.

  2. Metal ion-humic acid nanoparticle interactions: role of both complexation and condensation mechanisms.

    Science.gov (United States)

    Town, Raewyn M; van Leeuwen, Herman P

    2016-07-21

    Purely Donnan type models for electrostatic binding by humic acid (HA) nanoparticles are shown to be physically incomplete. To describe the extent of ion binding by HA, such models need to invoke parameters that are not consistent with experimental observations. These disparate parameters include anomalously high Donnan potentials, as well as intrinsic affinity constants for electrostatically associating ions such as Ca(2+). In contrast, the recently introduced counterion condensation - Donnan model (CCD) provides a physicochemically realistic description of the electrostatic contribution to metal ion binding by humic acid nanoparticles. The extent of Ca(2+)-HA association can be adequately described solely in terms of electrostatics only, including counterion condensation in the intraparticulate double layer in addition to Donnan partitioning in the remainder of the particle body. The binding of Cd(ii), Pb, (ii) and Cu(ii) by HA also involves inner-sphere complex formation leading to intraparticulate metal species distributions with major proportions of condensed and complexed ions.

  3. Dense Metal Plasma in a Solenoid for Ion Beam Neutralization

    Energy Technology Data Exchange (ETDEWEB)

    Anders, Andre; Kauffeldt, Marina; Oks, Efim M.; Roy, Prabir K.

    2010-10-30

    Space-charge neutralization is required to compress and focus a pulsed, high-current ion beam on a target for warm dense matter physics or heavy ion fusion experiments. We described approaches to produce dense plasma in and near the final focusing solenoid through which the ion beam travels, thereby providing an opportunity for the beam to acquire the necessary space-charge compensating electrons. Among the options are plasma injection from pulsed vacuum arc sources located outside the solenoid, and using a high current (> 4 kA) pulsed vacuum arc plasma from a ring cathode near the edge of the solenoid. The plasma distribution is characterized by photographic means, by an array of movable Langmuir probes, by a small single probe, and by evaluating Stark broadening of the Balmer H beta spectral line. In the main approach described here, the plasma is produced at several cathode spots distributed azimuthally on the ring cathode. It is shown that the plasma is essentially hollow, as determined by the structure of the magnetic field, though the plasma density exceeds 1014 cm-3 in practically all zones of the solenoid volume if the ring electrode is placed a few centimeters off the center of the solenoid. The plasma is non-uniform and fluctuating, however, since its density exceeds the ion beam density it is believed that this approach could provide a practical solution to the space charge neutralization challenge.

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

    African Journals Online (AJOL)

    GREGO

    2007-04-02

    diffusion control- led, even though these two different mechanisms cannot be sharply demarcated (Okieimen et al., 1987). In this study the rate of adsorption of Cu(II) and Zn(II) ions onto dyed coconut pollens was investigated at pH of.

  5. Metal Ion Activation of Clostridium sordellii Lethal Toxin and Clostridium difficile Toxin B

    Directory of Open Access Journals (Sweden)

    Harald Genth

    2016-04-01

    Full Text Available Lethal Toxin from Clostridium sordellii (TcsL and Toxin B from Clostridium difficile (TcdB belong to the family of the “Large clostridial glycosylating toxins.” These toxins mono-O-glucosylate low molecular weight GTPases of the Rho and Ras families by exploiting UDP-glucose as a hexose donor. TcsL is casually involved in the toxic shock syndrome and the gas gangrene. TcdB—together with Toxin A (TcdA—is causative for the pseudomembranous colitis (PMC. Here, we present evidence for the in vitro metal ion activation of the glucosyltransferase and the UDP-glucose hydrolysis activity of TcsL and TcdB. The following rating is found for activation by divalent metal ions: Mn2+ > Co2+ > Mg2+ >> Ca2+, Cu2+, Zn2+. TcsL and TcdB thus require divalent metal ions providing an octahedral coordination sphere. The EC50 values for TcsL were estimated at about 28 µM for Mn2+ and 180 µM for Mg2+. TcsL and TcdB further require co-stimulation by monovalent K+ (not by Na+. Finally, prebound divalent metal ions were dispensible for the cytopathic effects of TcsL and TcdB, leading to the conclusion that TcsL and TcdB recruit intracellular metal ions for activation of the glucosyltransferase activity. With regard to the intracellular metal ion concentrations, TcsL and TcdB are most likely activated by K+ and Mg2+ (rather than Mn2+ in mammalian target cells.

  6. Synthesis and metal ion binding properties of thiaaza crown macrocycles

    Energy Technology Data Exchange (ETDEWEB)

    Alp, Hakan [Department of Chemistry, Faculty of Arts and Sciences, Giresun University, 28049 Giresun (Turkey); Goek, Halil Zeki; Kantekin, Halit [Department of Chemistry, Faculty of Arts and Sciences, KTU, 61080 Trabzon (Turkey); Ocak, Ummuehan [Department of Chemistry, Faculty of Arts and Sciences, KTU, 61080 Trabzon (Turkey)], E-mail: ummuhanocak@yahoo.com

    2008-11-30

    Two new macrocyclic ligands (3) and (4), containing nitrogen-sulfur donor atoms, were designed and synthesized in a multi-step reaction sequence. The macrocycles (3) and (4) were used in solvent extraction of metal picrates such as Ag{sup +}, Hg{sup 2+}, Cd{sup 2+}, Zn{sup 2+}, Cu{sup 2+}, Ni{sup 2+}, Mn{sup 2+}, Co{sup 2+}, and Pb{sup 2+} from aqueous phase to the organic phase. The metal picrate extractions were investigated at 25 {+-} 0.1 deg. C by using UV-visible spectrometry. The extractability and selectivity of the mentioned metal picrates were evaluated according to the organic solvents. The values of the extraction constants (log K{sub ex}) and the complex compositions were determined for the extracted complexes.

  7. Ion beam effects of 26.0 MeV Cu{sup 7+} ions in thin metallic and insulating films during Heavy Ion ERDA measurements

    Energy Technology Data Exchange (ETDEWEB)

    Mavhungu, H. [NECSA, Radiation Science Division, PLABS, P.O. Box 582, Pretoria 0001 (South Africa); University of Pretoria, Department of Physics, Private Bag X20 Hatfield, Pretoria 0028 (South Africa); Msimanga, M., E-mail: msimangam@tut.ac.za [Tshwane University of Technology, Department of Physics, P Bag X680, Pretoria 0001 (South Africa); iThemba LABS, National Research Foundation, P. Bag 11, WITS 2050, Johannesburg (South Africa); Hlatshwayo, T. [University of Pretoria, Department of Physics, Private Bag X20 Hatfield, Pretoria 0028 (South Africa)

    2015-04-15

    We report on an investigation carried out to determine effects of the probing beam on the structure of typical metallic and insulating thin films during Elastic Recoil Detection Analysis (ERDA) using a heavy ion beam. Metallic niobium nitride (NbN) and insulating calcium fluoride (CaF{sub 2}) thin films (used as test samples) were irradiated by 26.0 MeV {sup 63}Cu{sup 7+} ions to fluences of 1.70 × 10{sup 14} ions/cm{sup 2} and 2.70 × 10{sup 14} ions/cm{sup 2}, respectively. The effects of irradiation on the structural properties of the films were studied using Rutherford Backscattering Spectrometry (RBS), X-ray diffraction (XRD) and Atomic Force Microscopy (AFM). RBS results showed a significant (18%) reduction in the thickness of the CaF{sub 2} film due to electronic sputtering compared to only 1% reduction in the NbN film. XRD results showed no significant peak shifts in both films, but rather formation of unidentified peaks in the insulating film. AFM results indicated a substantial decrease in the average surface roughness of the insulating film and only a nominal increase in that of the metallic film. Results of electronic sputtering yield measurements carried out by ERDA are explained in terms of both the Coulomb explosion and the inelastic thermal spike models.

  8. Natural Jordanian zeolite: removal of heavy metal ions from water samples using column and batch methods.

    Science.gov (United States)

    Baker, Hutaf M; Massadeh, Adnan M; Younes, Hammad A

    2009-10-01

    The adsorption behavior of natural Jordanian zeolites with respect to Cd(2 + ), Cu(2 + ), Pb(2 + ), and Zn(2 + ) was studied in order to consider its application to purity metal finishing drinking and waste water samples under different conditions such as zeolite particle size, ionic strength and initial metal ion concentration. In the present work, a new method was developed to remove the heavy metal by using a glass column as the one that used in column chromatography and to make a comparative between the batch experiment and column experiment by using natural Jordanian zeolite as adsorbent and some heavy metals as adsorbate. The column method was used using different metal ions concentrations ranged from 5 to 20 mg/L with average particle size of zeolite ranged between 90 and 350 mum, and ionic strength ranged from 0.01 to 0.05. Atomic absorption spectrometry was used for analysis of these heavy metal ions, the results obtained in this study indicated that zeolitic tuff is an efficient ion exchanger for removing heavy metals, in particular the fine particle sizes of zeolite at pH 6, whereas, no clear effect of low ionic strength values is noticed on the removal process. Equilibrium modeling of the removal showed that the adsorption of Cd(2 + ), Cu(2 + ), Pb(2 + ), and Zn(2 + ) were fitted to Langmuir, Freundlich and Dubinin-Kaganer-Radushkevich (DKR). The sorption energy E determined in the DKR equation (9.129, 10.000, 10.541, and 11.180 kJ/mol for Zn(2 + ), Cu(2 + ), Cd(2 + ) and Pb(2 + ) respectively) which revealed the nature of the ion-exchange mechanism.

  9. 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.

  10. Quantum dot impregnated-chitosan film for heavy metal ion sensing and removal.

    Science.gov (United States)

    Jaiswal, Amit; Ghsoh, Siddhartha Sankar; Chattopadhyay, Arun

    2012-11-06

    We report the use of biopolymer-stabilized ZnS quantum dots (Q-dots) for cation exchange reaction-based easy sensing and removal of heavy metal ions such as Hg(2+), Ag(+), and Pb(2+) in water. Chitosan-stabilized ZnS Q-dots were synthesized in aqueous medium and were observed to have been converted to HgS, Ag(2)S, and PbS Q-dots in the presence of corresponding ions. The transformed Q-dots showed characteristic color development, with Hg(2+) being exceptionally identifiable due to the visible bright yellow color formation, while brown coloration was observed in other metal ions. The cation exchange was driven by the difference in the solubility product of the reactant and the product Q-dots. The cation exchanged Q-dots preserved the morphology of the reactant Q-dots and displayed volume increase based on the bulk crystal lattice parameters. The band gap of the transformed Q-dots showed a major increase from the corresponding bulk band gap of the material, demonstrating the role of quantum confinement. Next, we fabricated ZnS Q-dot impregnated chitosan film which was used to remove heavy metal ions from contaminated water as measured using atomic absorption spectroscopy (AAS). The present system could suitably be used as a simple dipstick for elimination of heavy metal ion contamination in water.

  11. pH- and Metal Ion- Sensitive Hydrogels based on N-[2-(dimethylaminoethylacrylamide

    Directory of Open Access Journals (Sweden)

    Leena Nebhani

    2016-06-01

    Full Text Available Smart hydrogels are promising materials for actuators and sensors, as they can respond to small changes in their environment with a large property change. Hydrogels can respond to a variety of stimuli, for example temperature, pH, metal ions, etc. In this article, the synthesis and characterization of polyampholyte hydrogels based on open chain ligands showing pH and metal ion sensitivity are described. Copolymer and terpolymer gels using different mixtures of monomers i.e., N-[2-(dimethylaminoethylacrylamide] (DMAEAAm, N,N-dimethylacrylamide (DMAAm, acrylic acid (AA and 2-acrylamido-2-methyl-1-propanesulphonic acid (AMPS, have been synthesized. The effect of copolymer composition, i.e., the ratio and amount of ionic monomers and the degree of crosslinking on the swelling characteristics, was evaluated as a function of pH. On this basis, metal ion sensitivity measurements were performed at selected pH values. The metal ion sensitivity was measured by varying the concentration of Cu2+, Zn2+ and Ag+ ions under acidic pH conditions.

  12. Syntheses and optical and electrochemical properties of porphyrin dimers linked by metal ions.

    Science.gov (United States)

    Richeter, Sébastien; Jeandon, Christophe; Gisselbrecht, Jean-Paul; Ruppert, Romain; Callot, Henry J

    2002-05-29

    The preparation, isolation, and characterization of several new peripherally functionalized monomeric porphyrins and metalloporphyrins and of porphyrin dimers are described. These dimers are obtained by linking with metal ions two monomeric porphyrins bearing at their periphery an enaminoketone chelate fully conjugated with the aromatic ring. Porphyrin dimers linked by metal ions display large interactions in the ground state as evidenced by their electronic spectra and their electrochemical behavior. Compared to the monomeric analogue, these dimers show absorption spectra with intensified red-shifted Q-bands and their first oxidation potentials are substantially lowered and split into two distinct redox steps.

  13. Adsorption of heavy metal ions, dyes and proteins by chitosan composites and derivatives — A review

    Science.gov (United States)

    Liu, Bingjie; Wang, Dongfeng; Yu, Guangli; Meng, Xianghong

    2013-09-01

    Chitosan composites and derivatives have gained wide attentions as effective biosorbents due to their low costs and high contents of amino and hydroxyl functional groups. They have showed significant potentials of removing metal ions, dyes and proteins from various media. Chemical modifications that lead to the formation of the chitosan derivatives and chitosan composites have been extensively studied and widely reported in literatures. The aims of this review were to summarize the important information of the bioactivities of chitosan, highlight the various preparation methods of chitosan-based active biosorbents, and outline its potential applications in the adsorption of heavy metal ions, dyes and proteins from wastewater and aqueous solutions.

  14. Heavy Metal Ions Adsorption from Wastewater Using Activated Carbon from Orange Peel

    Directory of Open Access Journals (Sweden)

    Juan Carlos Moreno-Piraján

    2012-01-01

    Full Text Available Activated carbon obtained from orange peel (ACOP was synthesized and used for the removal of heavy metal ions (Cr, Cd, and Co from aqueous solutions. Two different adsorption models were used for analyzing data. Adsorption capacities were determined: copper ions exhibit the greatest adsorption on activated carbon orange peel because of its size and pH conditions. Adsorption capacity varies as a function of pH. Adsorption isotherms from aqueous solution of heavy metals on ACOP were determined. Adsorption isotherms are consistent with Langmuir's adsorption model. Adsorbent quantity and immersion enthalpy were studied.

  15. EPR-based approach for the localization of paramagnetic metal ions in biomolecules.

    Science.gov (United States)

    Abdullin, Dinar; Florin, Nicole; Hagelueken, Gregor; Schiemann, Olav

    2015-02-02

    Metal ions play an important role in the catalysis and folding of proteins and oligonucleotides. Their localization within the three-dimensional fold of such biomolecules is therefore an important goal in understanding structure-function relationships. A trilateration approach for the localization of metal ions by means of long-range distance measurements based on electron paramagnetic resonance (EPR) is introduced. The approach is tested on the Cu(2+) center of azurin, and factors affecting the precision of the method are discussed. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Clean and efficient extraction of copper ions and deposition as metal

    Directory of Open Access Journals (Sweden)

    Hassan H. Elsentriecy

    2015-07-01

    Full Text Available A simple, clean and efficient one-pot process is offered as an alternative to the conventional complex processing presently used to extract copper ions from copper containing materials, like copper concentrate or slag, and to form copper metal. The alternative process uses a eutectic molten salt of potassium chloride, sodium chloride and zinc chloride as the reaction fluid which is recyclable, low in cost, environmentally benign, low melting (melting point 204°, high boiling (vapor pressure is only a few psi at 800° and chemically, thermally and physically stable. The metal completely dissolves out of copper concentrate or slag in the aerobic eutectic molten chloride salt in a graphite or glassy carbon pot, which serves as a cathode, with a graphite anode, to reduce the metal ions to metal which sinks to the bottom of the graphite pot. The total efficiency for extraction and deposition is virtually 100% as determined by elemental and gravimetric analyses.

  17. Pesticides Curbing Soil Fertility: Effect of Complexation of Free Metal Ions

    KAUST Repository

    Kaur, Sukhmanpreet

    2017-07-04

    Researchers have suggested that the reason behind infertility is pernicious effect of broad spectrum pesticides on non target, beneficial microorganism of soil. Here, studying the chelating effect of selective organophosphate and carbamate pesticides with essential metal ions, at all possible combinations of three different pH (4 ± 0.05, 7 ± 0.05 and 9 ± 0.05) and three different temperatures (15 ± 0.5°C, 30 ± 0.5°C and 45 ± 0.5°C), shows very fast rate of reaction which further increases with increase of pH and temperature. Carbonyl oxygen of carbamate and phosphate oxygen of organophosphate were found to be common ligating sites among all the complexes. Formed metal complexes were found to be highly stable and water insoluble on interaction with essential metal ions in solvent medium as well as over silica. Density functional theory (DFT) calculations not only reinforced the experimental observations, but, after a wide computational conformational analysis, unraveled the nature of the high stable undesired species that consist of pesticides complexed by metal ions from the soil. All in all, apart from the direct toxicity of pesticides, the indirect effect by means of complexation of free metal ions impoverishes the soil.

  18. Efficient and selective adsorption of multi-metal ions using sulfonated cellulose as adsorbent.

    Science.gov (United States)

    Dong, Cuihua; Zhang, Fulong; Pang, Zhiqiang; Yang, Guihua

    2016-10-20

    Contamination of heavy metal in wastewater has caused great concerns on human life and health. Developing an efficient material to eliminate the heavy metal ions has been a popular topic in recent years. In this work, sulfonated cellulose (SC) was explored as efficient adsorbent for metal ions in solution. Thermo gravimetric analyzer (TGA), X-ray diffraction (XRD) and Fourier-transform infrared spectrometer (FTIR) first analyzed the characterizations of SC. Subsequently, effects of solution pH, adsorbent loading, temperature and initial metal ion concentration on adsorption performance were investigated. The results showed that sulfonated modification of cellulose could decrease the crystallinity and thermostability of cellulose. Due to its excellent performance of adsorption to metal ions, SC could reach adsorption equilibrium status within as short as 2min. In multi-component solution, SC can orderly removes Fe(3+), Pb(2+) and Cu(2+) with excellent selectivity and high efficiency. In addition, SC is a kind of green and renewable adsorbent because it can be easily regenerated by treatment with acid or chelating liquors. The mechanism study shows that the sulfonic group play a major role in the adsorption process. Copyright © 2016 Elsevier Ltd. All rights reserved.

  19. Mechanism of Metal Ion Activation of the Diphtheria Toxin Repressor DtxR

    Energy Technology Data Exchange (ETDEWEB)

    D' Aquino,J.; Tetenbaum-Novatt, J.; White, A.; Berkovitch, F.; Ringe, D.

    2005-01-01

    The diphtheria toxin repressor (DtxR) is a metal ion-activated transcriptional regulator that has been linked to the virulence of Corynebacterium diphtheriae. Structure determination has shown that there are two metal ion binding sites per repressor monomer, and site-directed mutagenesis has demonstrated that binding site 2 (primary) is essential for recognition of the target DNA repressor, leaving the role of binding site 1 (ancillary) unclear. Calorimetric techniques have demonstrated that although binding site 1 (ancillary) has high affinity for metal ion with a binding constant of 2 x 10{sup -7}, binding site 2 (primary) is a low-affinity binding site with a binding constant of 6.3 x 10{sup -4}. These two binding sites act in an independent fashion, and their contribution can be easily dissected by traditional mutational analysis. Our results clearly demonstrate that binding site 1 (ancillary) is the first one to be occupied during metal ion activation, playing a critical role in stabilization of the repressor. In addition, structural data obtained for the mutants Ni-DtxR(H79A, C102D), reported here, and the previously reported DtxR(H79A) have allowed us to propose a mechanism of metal activation for DtxR.

  20. Pesticides Curbing Soil Fertility: Effect of Complexation of Free Metal Ions

    Science.gov (United States)

    Kaur, Sukhmanpreet; Kumar, Vijay; Chawla, Mohit; Cavallo, Luigi; Poater, Albert; Upadhyay, Niraj

    2017-07-01

    Researchers have suggested that the reason behind infertility is pernicious effect of broad spectrum pesticides on non target, beneficial microorganism of soil. Here, studying the chelating effect of selective organophosphate and carbamate pesticides with essential metal ions, at all possible combinations of three different pH (4±0.05, 7±0.05 and 9±0.05) and three different temperatures (15±0.5°C, 30±0.5°C and 45±0.5°C), shows very fast rate of reaction which further increases with increase of pH and temperature. Carbonyl oxygen of carbamate and phosphate oxygen of organophosphate were found to be common ligating sites among all the complexes. Formed metal complexes were found to be highly stable and water insoluble on interaction with essential metal ions in solvent medium as well as over silica. Density functional theory (DFT) calculations not only reinforced the experimental observations, but, after a wide computational conformational analysis, unraveled the nature of the high stable undesired species that consist of pesticides complexed by metal ions from the soil. All in all, apart from the direct toxicity of pesticides, the indirect effect by means of complexation of free metal ions impoverishes the soil.

  1. Energetic metallic ion implantation in polymers via cost-effective laser-driven ion source

    Science.gov (United States)

    Tahir, Muhammad Bilal; Rafique, M. Shahid; Ahmed, Rabia; Rafique, M.; Iqbal, Tahir; Hasan, Ali

    2017-07-01

    This research work reports the ions emission from the plasma generated by Nd:YAG laser having wavelength 1.064 μm, power 1.1 MW, pulse energy 10 mJ and intensity 1011 W/cm2 irradiated at 70° with respect to the target normal to the ions. These ions were accelerated through a home-made extraction assembly by means of a high voltage DC power supply. The energy of these ions were measured using Thomson parabola technique which utilizes Solid State Nuclear Track Detector (CR-39) and confirmed by Faraday cup as well that exploits a well-known technique known as time of flight. Interestingly, a significant increase in energy (from 490 to 730 keV) was observed with a discrete increase in acceleration potential from 0 to 18 kV. Polyethylene terephthalate (PET) and polypropylene were exposed to this recently developed ion source facility, to authenticate the reliability of this facility. The surface of the polymer is affected when energy of the irradiated ion is increased, which is evident from the optical micrographs. An increase in electrical conductivity was also observed with the increase in ion energy.

  2. The synergistic antibacterial activity and mechanism of multicomponent metal ions-containing aqueous solutions against Staphylococcus aureus.

    Science.gov (United States)

    Wang, Xiaolan; Liu, Shaoxiang; Li, Mei; Yu, Peng; Chu, Xiao; Li, Lihua; Tan, Guoxin; Wang, Yingjun; Chen, Xiaofeng; Zhang, Yu; Ning, Chengyun

    2016-10-01

    Silver (Ag+), zinc (Zn2+) and copper (Cu2+) ions, are well known for their broad-spectrum antibacterial activities while generating low resistance. However, whether or multiple metal ions in aqueous solutions acted synergistically or antagonistically antimicrobial properties, remained unknown. Therefore, it was of great significance to investigate the antibacterial properties of multicomponent metal ions-containing aqueous solutions. In this study, the antibacterial activities of multicomponent metal ions-containing aqueous solutions were investigated for the first time. We found that the antibacterial activities of multicomponent metal ions-containing aqueous solutions were higher than those of single metal ion-containing aqueous solution. Furthermore, the synergistic antibacterial mechanism of these multicomponent metal ions-containing aqueous solutions was first investigated. The generation of reactive oxygen species (ROS) through electron transfer in the enzymes and Fenton reactions formed the main synergistic antibacterial mechanism of the multicomponent metal ions-containing aqueous solutions. Therefore, the encouraging results demonstrate the great potential applications of multicomponent metal ions for the design of new biomaterials or prosthesis containing Ag-Cu-Zn alloy which can release Ag+, Zn2+ and Cu2+ and minimize the risk of hospital acquired infection. Copyright © 2016 Elsevier Inc. All rights reserved.

  3. Heavy metal ions adsorption by suspended particle and sediment of ...

    African Journals Online (AJOL)

    GREGORY

    2012-01-10

    Jan 10, 2012 ... samples in the laboratory, standard metals including Pb, Cu, Zn and Fe (15, 5, 5, and 5 mg/l, respectively) and sediments from the three stations, both arranged in the .... process, lead is separated from gold, silver, zinc and iron but much lead is deposited in waste. Figure 1 shows the situation of the Sorb ...

  4. Bioleaching of metal ions from low grade sulphide ore: Process ...

    African Journals Online (AJOL)

    STORAGESEVER

    2010-05-10

    May 10, 2010 ... 1Hubei Key Laboratory of Novel Reactor and Green Chemical Technology, Wuhan Institute of Technology, Wuhan, China. ... 10%, temperature 47°C and agitation 180 rpm, the percent bioleachabilities of metals were Zn 72%, Co .... sources of the laboratory medium in the bioleaching process. The.

  5. Ternary Complexes of some Divalent Metal Ions with Potentially ...

    African Journals Online (AJOL)

    ... and residual analysis. The predominant species detected were ML2XH2, MLXH2 and MLX2 for Ca(II), Mg(II) and Zn(II). The formation and distribution of different species with relative concentrations of metal and ligands with varying pH are represented in the form of distribution diagrams. The influence of the solvent on the ...

  6. Heavy metal ions adsorption by suspended particle and sediment of ...

    African Journals Online (AJOL)

    Nowadays, it is important to evaluate the self-purifying capacity of rivers because of the different kinds of pollutants discharged into them. Important kind of pollutants and heavy metals exist in wastewaters industries. When the Sorb Dona mine is placed in Upper Chalus River, in the west of Mazandaran, products of mine ...

  7. Adsorption of strontium (II) metal ions using phosphonate ...

    Indian Academy of Sciences (India)

    The metal binding was examined by the energy dispersive spectroscopy and scanning electron microscopy for the adsorbed Sr(II). Batch adsorption studies were performed by varying three parameters, namely initial pH, adsorbentdose and the contact time. The reaction kinetics was determined by the Langmuir, Freundlich, ...

  8. Preparation of magnetic carboxymethylchitosan nanoparticles for adsorption of heavy metal ions

    OpenAIRE

    Charpentier, Thibaut V.J.; Neville, Anne; Lanigan, Joseph L; Barker, Richard; Smith, Margaret J.; Richardson, Thomas

    2016-01-01

    The remediation of metal and heavy metal contaminants from water ecosystems is a long-standing problem in the field of water management. The development of efficient, cost effective, and environmentally friendly natural polymer-based adsorbents is reported here. Magnetic chitosan (CS) and carboxymethylchitosan (CMC) nanocomposites have been synthesized by a simple one-step chemical coprecipitation method. The nanoparticles were assessed for the removal of Pb2+, Cu2+, and Zn2+ ions from aqueou...

  9. Martian Metallic Ions Deposited by Comet Siding Spring Defy Expectations

    Science.gov (United States)

    Crismani, Matteo; Schneider, Nicholas M.; Plane, John; Jain, Sonal; Deighan, Justin; Yelle, Roger V.; Evans, J. Scott

    2017-10-01

    On October 19th 2014, comet C/2013 A1 (Siding Spring) had a close encounter with Mars and deposited cometary dust particles into the Martian atmosphere. Dust that impacted Mars was readily identifiable as the meteoric deposition of Mg, Fe, Na, etc. by the Imaging Ultraviolet Spectrograph (IUVS) and Neutral Gas and Ion Mass Spectrometer (NGIMS) on the NASA Mars Atmosphere and Volatile EvolutioN (MAVEN) spacecraft. While Mg+ from comet Siding Spring and in a persistent layer was identified previously by IUVS, this is the first remote sensing report on the abundance, spatial distribution and temporal evolution of Mg, Fe, and Fe+. Subsequent evolution of the distributions of ions and neutrals indicate distinct physical mechanisms for distribution. We find vertical and latitudinal inhomogeneities that are inconsistent with expected dynamical transport mechanisms.

  10. [Thermodynamic approach to the selection of polyuronide sequestrants for protection of the human body from toxic metal ions. Interactions of polyuronides with lead ions].

    Science.gov (United States)

    Braudo, E E; Danilova, I V; Dianova, V T; Kobak, V V; Plashchina, I G

    2001-01-01

    Binding isotherms of Pb2+ ions with potassium pectate and potassium alginate with relatively low content of blocks of L-guluronic residues (20%) have been determined. Interactions of Pb2+ ions with polyuronides studied is cooperative. Maximum values of binding constants are an order of magnitude higher than previously determined ones for Ca2+ and Sr2+ ions. Along with ion-coordination ("stoichiometric") interactions, alginate is typified by so-called extra-stoichiometric binding of Pb2+ ions, which presumably proceeds by a coprecipitation mechanism. Limitations of the thermodynamic approach to the selection of sequestrants for human body protection from toxic metal ions are discussed.

  11. Adsorption of Heavy Metal Ions to Floc-Type Biosorbents

    OpenAIRE

    Seki, Hideshi; Suzuki, Akira

    2002-01-01

    Adsorption of cadmium and lead ions to floc-type biosorbents was reported in this work. Two types of biosorbents containing a marine microalga, Heterosigma akashiwo (Hada) Hada or a purple non-sulfur bacterium, Rhodobacter sphaeroides were prepared. The microorganisms inactivated by steam sterilization were immobilized in casein floc and cross-linked with glutaraldehyde. In the present immobilizing method, we obtained the biosorbents comprising as much as 67% of microorganism on a dry-weight ...

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

    African Journals Online (AJOL)

    Michael Horsfall

    bioavailability are 95.83% to 99.84% at the pH ranges of 6.1 to 7.8 of the tested wells. Iron as free Fe2+ was bioavailable at 46.53% to 79.37% of the total iron. The lower values of free Fe2+ ions are related to the organic ... calcium, magnesium, potassium and iron in groundwater using geochemical models from the.

  13. Metal Ions Activate Vascular Endothelial Cells and Increase Lymphocyte Chemotaxis and Binding

    Science.gov (United States)

    Ninomiya, James T.; Kuzma, Scott A.; Schnettler, Timothy J.; Krolikowski, John G.; Struve, Janine A.; Weihrauch, Dorothee

    2014-01-01

    Metal on metal articulations in hip arthroplasty offer advantages, including lower volumetric wear compared to conventional metalonpolyethylene bearings, and increased resistance to dislocation. Reports described early failures, with histologic features similar to a Type IV immune response. Mechanisms by which metal wear products cause this reaction are not completely understood. We hypothesized a mechanism through direct activation of endothelial cells (ECs) by metal ions, resulting in both vasculitis and accumulation of lymphocytes without prior immune sensitization. Effects of metal ions were evaluated using human ECs in culture. Alterations in chemotactic proteins IL8 and MCP1 were assessed, as was upregulation of the adhesion molecule ICAM-1 and lymphocyte binding to ECs. Cobalt increased secretion of IL8 and MCP1 significantly, and upregulated the expression of ICAM-1 in ECs compared to stimulation by chromium and controls. Binding of lymphocytes to ECs and transEC migration were both significantly increased by cobalt but not chromium. These findings suggest that cobalt contributes more to the activation of ECs and lymphocyte binding than chromium without an allergic response. Some of the adverse tissue reactions to implants with components made of cobalt–chromium–molybdenium alloys may be due in part to activation of the endothelium by metal ions. PMID:23629852

  14. Effect on the concentration and metal ion concentration for the degradation of wastewater

    Science.gov (United States)

    Chen, M. T.; He, L. F.; Yu, W. Q.; Huo, J. H.; Xu, C. H.; Li, Z. Y.; Jiang, Z. X.

    2017-11-01

    The advanced oxidation technology based on the theory of sulfate radicals has been extensively studied. In this paper, the degradation of methyl orange over the transition metal catalysts and the catalytic effect on various metal ion catalysts were investigated. The wastewater degradation experiments were judged by the degradation rate and pH under the optimal conditions. In this study, the methyl orange was used as the simulation of the printing and dyeing wastewater, and the experiment was carried out. The vary concentration of methyl orange and metal ions were carried out.. The results showed that persulfate were activated by the metal salts the cobalt metal ions exhibited the strongest performance. The resulted indicated that the methyl orange degradation of 40 mg/L was the appropriate concentration. from varied from 40 mg/L to 120 mg/L interval 20 mg/L, and the catalytic activity of 2g m/L is the best dose at six metal concentrations of 0.5 mg/L, 1 mg/L, 2 mg/L, 3 mg/L, 4 mg/L and 5 mg/L, which provided a very rational basis for the treatment of the practical wastewater.

  15. Pillared metal organic frameworks for the luminescence sensing of small molecules and metal ions in aqueous solutions.

    Science.gov (United States)

    Liu, Fu-Hong; Qin, Chao; Ding, Yan; Wu, Han; Shao, Kui-Zhan; Su, Zhong-Min

    2015-01-28

    Two novel pillared MOFs (metal organic frameworks) [Zn2(trz)2(tda)]·DMA CH3OH (1) and [Zn2(trz)2(bpdc)]·DMA (2) were obtained under solvothermal conditions. The resulting MOFs show similar structures but with different interlayer distances based on the different carboxylate ligands. 1 and 2 display a certain degree of framework stability in both acid/base solutions and water. The luminescence intensities of the activated phases 1a and 2a are sensitive to metal ions, particularly Fe(3+) and Cd(2+) ions. Furthermore, the luminescent properties of 1a and 2a well dispersed in different solvents have also been investigated systematically, which demonstrate distinct solvent-dependent luminescent spectra with emission intensities that are significantly quenched by acetone, nitrobenzene and trinitrotoluene.

  16. Binary ion exchange of metal ions in Y and X zeolites

    Directory of Open Access Journals (Sweden)

    M.A.S.D. Barros

    2003-10-01

    Full Text Available The ion exchange of Na for Cr/K, Cr/Mg and Cr/Ca in Y and X zeolites was studied using breakthrough curves. It was observed that Cr3+ ions were able to remove some competitive ions that had already been exchanged at the zeolitic sites, producing a sequential ion exchange. Some mass transfer parameters such as length of unused bed, overall mass transfer coefficient, operational ratio and dimensionless variance were studied. Chromium uptake was influenced much more by the competing ion in the NaX zeolite columns. The dimensionless variance indicated that Cr/K solution produced a greater axial dispersion than the Cr/Mg and Cr/Ca systems, probably due to some interaction between Cr3+ and K+ ions. The order of dynamic selectivity, provided by the cation uptake, was Cr3+ > Ca2+, Cr3+ > Mg2+ and Cr3+ > K+ for NaY zeolite and Ca2+ ~Cr3+, Mg2+ > Cr3+ and Cr3+ > K+ for NaX zeolite. Due to the more favorable mass transfer parameters and higher affinity for Cr3+, it was concluded that NaY zeolite was more efficient at chromium uptake in competitive systems.

  17. Metal-ion spin-on glasses: Novel materials for active waveguides

    Energy Technology Data Exchange (ETDEWEB)

    Ashby, C.I.H.; Sullivan, C.T.; Vawter, G.A.; Hohimer, J.P.; Hadley, G.R.; Neal, D.R.

    1993-12-31

    Monolithic integration of a rare-earth-ion-based active waveguide on the same wafer as its diode pump laser would permit compact packaging of the technology demonstrated in fiber lasers and amplifiers. This new monolithic technology would offer the potential for developing compact infrared and visible (up-conversion) lasers, amplifiers, and other photonic integrated circuit components. One approach that we are investigating for such monolithic integration uses a high concentration of one or more rare-earth ions incorporated into polysiloxane spin-on glasses that are solvent-cast onto III-V semiconductor wafers. This ``fiber on a chip`` technology substitute a relatively high-ion-concentration, short-length metal-ion spin-on glass (MISOG) waveguide for the low-ion-concentration, long-length fiber. Progress to data on developing MISOG waveguide materials and technology is discussed.

  18. Obtaining sorbents of metal ions based on yeast cells Rhodotorula glutinis

    Directory of Open Access Journals (Sweden)

    Zh. Tattibayeva

    2013-05-01

    Full Text Available Ability to separate Cu2+ and Pb2+ ions from solution using yeast cells Rhodotorulа glutinis were considered. The degree of water purification in this case is of 60-70%. To increase the degree of binding of metal ions with cells and facilitate separation processes of water sorbents their immobilization on the surface of the water in the presence of polyethyleneimine was carried out. It is shown that under optimal conditions on the surface of 1 g diatomite 18 ∙ 106 cells is adsorbed. The high sorption capacity of diatomite justified its porosity. IR spectroscopic study of the interaction of the ions Cu2+ and Pb2+ with cell surface showed that high affinity Pb2 + ions to the surface of yeast cells is connected with form of slightly soluble compounds with the phosphate ions.

  19. X-ray and fast ion generation from metal targets by femtosecond laser irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Okano, Yasuaki; Kishimura, Hiroaki; Hironaka, Yoichiro; Nakamura, Kazutaka G.; Kondo, Ken-ichi

    2002-09-30

    X-ray and fast ion generation has been studied by femtosecond laser irradiation (52 fs, 790 nm) on metal targets (copper and iron), where hard X-ray emission takes place at power density up to 10{sup 17} W/cm{sup 2}. X-ray intensities and kinetic energy distributions of ions are observed as a function of the power density. The ion energy distributions for each target show several peak components, which are fast ions (high-energy component in keV range), and additional low-energy component (a few hundreds of eV). Average fast ion energshow a strong dependence on the power density, and are comparable to ponderomotive potential.

  20. Effect of metallic nanoparticles in thin foils for laser ion acceleration

    Science.gov (United States)

    Torrisi, L.; Cutroneo, M.; Ceccio, G.

    2015-01-01

    Nanostructured materials having a high absorption coefficient for visible and near-IR wavelengths can be employed to enhance the laser light energy release in micrometric thin foils in order to generate hot non-equilibrium plasmas and to transfer higher ion acceleration energy. Thin polymeric films containing nanometric spheres of metals (Ti, Cu, Ag, and Au) can be employed to be laser irradiated in a high vacuum and to study the consequent plasma ion acceleration process. Infrared laser irradiations at 1010 W cm-2 intensity, 3 ns pulse duration, and 1064 nm wavelength were employed to produce plasma accelerating ions in the backward direction. Measurements have demonstrated that the presence of nanostructures significantly increases the laser absorption effect and consequently the plasma electron temperature and density and the electric field driving the ion acceleration. Target preparation will be extended to submit thin targets to high laser intensity irradiation above 1015 W cm-2, where the effect of ion acceleration should be enhanced.

  1. Metal ion selectivities of the highly preorganized tetradentate ligand 1,10-phenanthroline-2,9-dicarboxamide with lanthanide(III) ions and some actinide ions

    Energy Technology Data Exchange (ETDEWEB)

    Merill, D.; Hancock, R.D. [North Carolina Univ., Wilmington, NC (United States). Dept. of Chemistry and Biochemistry

    2011-07-01

    Metal ion complexing properties of the ligand PDAM (1,10-phenanthroline-2,9-dicarboxamide) are reported in relation to its possible use as a functional group for solvent extractants in the separation of Am(III) from Ln(III) (lanthanide) ions. PDAM is only slightly water soluble, but variation of the intense {pi}-{pi}{sup *} transitions in the UV spectrum of 2 x 10{sup -5} M PDAM solutions as a function of pH or metal ion concentration allowed for the determination of the protonation constant (pK) and logK{sub 1} values with metal ions. The pK of PDAM is 0.6 {+-} 0.1 in 1.0 M NaClO{sub 4}, the lowest for any 1,10-phenanthroline (phen) derivative (in contrast, pK phen=5.1), which is attributed to the electron-withdrawing properties of the amide substituents of PDAM. The weak proton basicity of PDAM may be an important factor in its use as the functional group of a solvent extractant from acidic solutions. The formation constants are determined by UV-Visible spectroscopy for the Ln(III) ions from La(III) to Lu(III) (excluding Pm(III)), as well as for Y(III), Sc(III), Th(IV), and the UO{sub 2}{sup 2+} cation in 0.1 M NaClO{sub 4} at 25 C. The log K{sub 1} values for the Ln(III) ions show only small changes from La(III) to Lu(III) (both have log K{sub 1} = 3.80). The amide O-donors (oxygen donors) of the amide groups of PDAM appear to cause considerable stabilization of the complexes of PDAM as compared to those of phen, consistent with the idea that the neutral O-donor is a strong Lewis base towards large metal ions such as the Ln(III) ions. A reviewer has pointed out that the amide groups would also stabilize the complexes of PDAM by virtue of the chelate effect, in that PDAM is tetradentate, while phen is only bidentate. The small change in complex stability for PDAM complexes in passing from La(III) to Lu(III) is rationalized in terms of the idea that neutral O-donors stabilize the complexes of the large La(III) ion more than the smaller Lu(III) ion, offsetting the

  2. Divalent metal ions enhance DOPAL-induced oligomerization of alpha-synuclein.

    Science.gov (United States)

    Jinsmaa, Yunden; Sullivan, Patricia; Gross, Daniel; Cooney, Adele; Sharabi, Yehonatan; Goldstein, David S

    2014-05-21

    Parkinson disease (PD) features profound striatal dopamine depletion and Lewy bodies containing abundant precipitated alpha-synuclein. Mechanisms linking alpha-synucleinopathy with the death of dopamine neurons remain incompletely understood. One such link may be 3,4-dihydroxyphenylacetaldehyde (DOPAL). All of the intra-neuronal metabolism of dopamine passes through DOPAL, which is toxic. DOPAL also potently oligomerizes alpha-synuclein and alpha-synuclein oligomers are thought to be pathogenic in PD. Another implicated factor in PD pathogenesis is metal ions, and alpha-synuclein contains binding sites for these ions. In this study we tested whether divalent metal ions augment DOPAL-induced oligomerization of alpha-synuclein in cell-free system and in PC12 cells conditionally over-expressing alpha-synuclein. Incubation with divalent metal ions augmented DOPAL-induced oligomerization of alpha-synuclein (Cu(2+)>Fe(2+)>Mn(2+)), whereas monovalent Cu(1+) and trivalent Fe(3+) were without effect. Other dopamine metabolites, dopamine itself, and metal ions alone or in combination with dopamine, also had no effect. Antioxidant treatment with ascorbic acid and divalent cation chelation with EDTA attenuated the augmentation by Cu(2+) of DOPAL-induced alpha-synuclein oligomerization. Incubation of PC12 cells with L-DOPA markedly increased intracellular DOPAL content and promoted alpha-synuclein dimerization. Co-incubation with Cu(2+) amplified (p=0.01), while monoamine oxidase inhibition prevented, L-DOPA-related dimerization of alpha-synuclein (p=0.01). We conclude that divalent metal ions augment DOPAL-induced oligomerization of alpha-synuclein. Drugs that interfere with this interaction might constitute a novel approach for future treatment or prevention approaches. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

  3. Use of multi-transition-metal-ion-exchanged zeolite 13X catalysts in methane emissions abatement

    Energy Technology Data Exchange (ETDEWEB)

    Hui, K.S.; Chao, C.Y.H.; Kwong, C.W.; Wan, M.P. [Department of Mechanical Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong (China)

    2008-04-15

    Methane is a potent greenhouse gas. It has a global warming potential (GWP) 23 times greater than carbon dioxide. Reducing methane emissions would lead to substantial economic and environmental benefits. This study investigated the performance of multi-transition-metal-(Cu, Cr, Ni, and Co)-ion-exchanged zeolite 13X catalysts in methane emissions abatement. The catalytic activity in methane combustion using multi-ion-exchanged catalysts was studied with different parameters including the molar percentage of metal loading, the space velocity, and the inlet methane concentration under atmospheric pressure and at a relatively low reaction temperature of 500 C. The performance of the catalysts was determined in terms of the apparent activation energy, the number of active sites of the catalyst, and the BET surface area of the catalyst. This study showed that multi-ion-exchanged catalysts outperformed single-ion-exchanged and acidified 13X catalysts and that lengthening the residence time led to a higher methane conversion percentage. The enhanced catalytic activity in the multi-ion-exchanged catalysts was attributed to the presence of exchanged transition ions instead of acid sites in the catalyst. The catalytic activity of the catalysts was influenced by the metal loading amount, which played an important role in affecting the apparent activation energy for methane combustion, the active sites, and the BET surface area of the catalyst. Increasing the amount of metal loading in the catalyst decreased the apparent activation energy for methane combustion and also the BET surface area of the catalyst. An optimized metal loading amount at which the highest catalytic activity was observed due to the combined effects of the various factors was determined. (author)

  4. Comparison of different transition metal ions for immobilized metal affinity chromatography of selenoprotein P from human plasma

    DEFF Research Database (Denmark)

    Sidenius, U; Farver, O; Jøns, O

    1999-01-01

    Cu2+, Ni2+, Zn2+, Co2+ and Cd2+ were evaluated in metal ion affinity chromatography for enrichment of selenoprotein P, and immobilized Co2+ affinity chromatography was found to be the most selective chromatographic method. The chromatography was performed by fast protein liquid chromatography and....... The purity of the protein was determined by SDS-PAGE and by sequencing from polyvinylidene difluoride blots of SDS-PAGE gels....

  5. Age and Smoking Related Changes in Metal Ion Levels in Human Lens: Implications for Cataract Formation.

    Science.gov (United States)

    Langford-Smith, Alex; Tilakaratna, Viranga; Lythgoe, Paul R; Clark, Simon J; Bishop, Paul N; Day, Anthony J

    2016-01-01

    Age-related cataract formation is the primary cause of blindness worldwide and although treatable by surgical removal of the lens the majority of sufferers have neither the finances nor access to the medical facilities required. Therefore, a better understanding of the pathogenesis of cataract may identify new therapeutic targets to prevent or slow its progression. Cataract incidence is strongly correlated with age and cigarette smoking, factors that are often associated with accumulation of metal ions in other tissues. Therefore this study evaluated the age-related changes in 14 metal ions in 32 post mortem human lenses without known cataract from donors of 11 to 82 years of age by inductively coupled plasma mass spectrometry; smoking-related changes in 10 smokers verses 14 non-smokers were also analysed. A significant age-related increase in selenium and decrease in copper ions was observed for the first time in the lens tissue, where cadmium ion levels were also increased as has been seen previously. Aluminium and vanadium ions were found to be increased in smokers compared to non-smokers (an analysis that has only been carried out before in lenses with cataract). These changes in metal ions, i.e. that occur as a consequence of normal ageing and of smoking, could contribute to cataract formation via induction of oxidative stress pathways, modulation of extracellular matrix structure/function and cellular toxicity. Thus, this study has identified novel changes in metal ions in human lens that could potentially drive the pathology of cataract formation.

  6. Age and Smoking Related Changes in Metal Ion Levels in Human Lens: Implications for Cataract Formation.

    Directory of Open Access Journals (Sweden)

    Alex Langford-Smith

    Full Text Available Age-related cataract formation is the primary cause of blindness worldwide and although treatable by surgical removal of the lens the majority of sufferers have neither the finances nor access to the medical facilities required. Therefore, a better understanding of the pathogenesis of cataract may identify new therapeutic targets to prevent or slow its progression. Cataract incidence is strongly correlated with age and cigarette smoking, factors that are often associated with accumulation of metal ions in other tissues. Therefore this study evaluated the age-related changes in 14 metal ions in 32 post mortem human lenses without known cataract from donors of 11 to 82 years of age by inductively coupled plasma mass spectrometry; smoking-related changes in 10 smokers verses 14 non-smokers were also analysed. A significant age-related increase in selenium and decrease in copper ions was observed for the first time in the lens tissue, where cadmium ion levels were also increased as has been seen previously. Aluminium and vanadium ions were found to be increased in smokers compared to non-smokers (an analysis that has only been carried out before in lenses with cataract. These changes in metal ions, i.e. that occur as a consequence of normal ageing and of smoking, could contribute to cataract formation via induction of oxidative stress pathways, modulation of extracellular matrix structure/function and cellular toxicity. Thus, this study has identified novel changes in metal ions in human lens that could potentially drive the pathology of cataract formation.

  7. Study of structural and spectroscopic behavior of Sm3+ ions in lead-zinc borate glasses containing alkali metal ions

    Science.gov (United States)

    Sasi Kumar, M. V.; Babu, S.; Rajeswara Reddy, B.; Ratnakaram, Y. C.

    2017-06-01

    High luminescence behavior of rare earth inorganic glasses have a variety of uses in the industry. In the past few decades, rare earth ions with characteristic photonics applications are being hosted by heavy metal oxide glasses. Among the rare earth ions Sm3+ ion has features which make it apt for high density optical storage. The authors of the paper have experimented to synthesize Sm3+ doped glasses. In this regard a new series of borate glasses doped with 1 mol% Sm3+ ion are developed by using melt-quenching technique. XRD, FTIR, optical absorption, luminescence techniques are used to study the various characteristics of Sm3+ ion in the present glass matrices. The XRD spectra confirms the amorphous nature of glasses. Further, the researchers have used differential thermal analysis to study the glass transition temperature. The structural groups in the prepared glasses are studied using Fourier transform infrared spectra. From the measurement of its optical absorption, three phenomenological Judd-Ofelt intensity parameters (Ω2, Ω4 and Ω6) have been computed. Based on these Judd-Ofelt intensity parameters, radiative properties such as radiative probabilities (Arad), branching ratios (β), and radiative life time (τR) are calculated. The excitation spectra of Sm3+ doped lithium heavy metal borate glass matrix is recorded under the emission wavelength of 600 nm. The emission spectra are recorded under 404 nm excitation wavelength. From various emission transitions, 4G5/2 → 6H7/2 and 4G5/2 → 6H9/2 bands could be of interest for various applications. The decay profiles of 4G5/2 level exhibit single exponential nature in all the prepared glass matrices. The potassium glass matrix exhibits higher quantum efficiency than the other glass matrices. Finally, by going through these several spectroscopic characterizations, it is concluded that the prepared Sm3+ doped lead-zinc borate glasses might be useful for visible light applications.

  8. Ternary Complexes of some Divalent Metal Ions with Potentially ...

    African Journals Online (AJOL)

    NICO

    studied in varying concentrations (0.0–60.0 % v/v) of 1, 4-dioxane-water mixtures maintaining an ionic strength of 0.16 mol L–1 sodium chloride at 303.0 K. ... enzymes, the activity of which is due to metal-enzyme-substrate complexes. The active .... static interaction is related to the dielectric constant of the medium and log Д ...

  9. Validation of Transfer Functions Predicting Cd and Pb Free Metal Ion Activity in Soil Solution as a Function of Soil Characteristics and Reactive Metal Content

    NARCIS (Netherlands)

    Pampura, T.; Groenenberg, J.E.; Lofts, S.; Priputina, I.

    2007-01-01

    According to recent insight, the toxicity of metals in soils is better related to the free metal ion (FMI) activity in the soil solution than to the total metal concentration in soil. However, the determination of FMI activities in soil solution is a difficult and time-consuming task. An alternative

  10. The essential roles of metal ions in insect homeostasis and physiology.

    Science.gov (United States)

    Dow, Julian At

    2017-10-01

    Metal ions play distinct roles in living organisms, including insects. Some, like sodium and potassium, are central players in osmoregulation and 'blood and guts' transport physiology, and have been implicated in cold adaptation. Calcium is a key player as a second messenger, and as a structural element. Other metals, particularly those with multiple redox states, can be cofactors in many metalloenzymes, but can contribute to toxic oxidative stress on the organism in excess. This short review selects some examples where classical knowledge has been supplemented with recent advances, in order to emphasize the importance of metals as essential nutrients for insect survival. Copyright © 2017 Elsevier Inc. All rights reserved.

  11. Double metal ions synergistic effect in hierarchical multiple sulfide microflowers for enhanced supercapacitor performance.

    Science.gov (United States)

    Gao, Yang; Mi, Liwei; Wei, Wutao; Cui, Shizhong; Zheng, Zhi; Hou, Hongwei; Chen, Weihua

    2015-02-25

    In this paper, the design, synthesis, and measurement of a new and hierarchically structured series of NixCo1-xS1.097 electroactive materials are reported. The materials were synthesized through an ion-exchange process using hierarchically structured CoS1.097 as precursors, and a strategy utilizing the synergistic effect of double metal ions was developed. Two complementary metal ions were used to enhance the performance of electrode materials. The specific capacitance of the electroactive materials was continuously improved by increasing the nickel ion content, and the electric conductivity was also enhanced when the cobalt ion was varied. Experimental results showed that the nickel ion content in NixCo1-xS1.097 could be adjusted from x = 0 to 0.48. Specifically, when x = 0.48, the composite exhibited a remarkable maximum specific capacitance approximately 5 times higher than that of the CoS1.097 precursors at a current density of 0.5 A g(-1). Furthermore, the specific capacitance of Ni0.48Co0.52S1.097 electrodes that were modified with reduced graphene oxide could reach to 1152 and 971 F g(-1) at current densities of 0.5 and 20 A g(-1) and showed remarkably higher electrochemical performance than the unmodified electrodes because of their enhanced electrical conductivity. Thus, the strategy utilizing the synergistic effect of double metal ions is an alternative technique to fabricate high-performance electrode materials for supercapacitors and lithium ion batteries.

  12. A novel malonamide bridged silsesquioxane precursor for enhanced dispersion of transition metal ions in hybrid silica membranes

    NARCIS (Netherlands)

    Besselink, R.; Qureshi, H.F.; Winnubst, Aloysius J.A.; ten Elshof, Johan E.

    2015-01-01

    Microporous hybrid silica membranes are known to have superior (hydro)thermal and chemical stability. By incorporating metal ions, such as Ce4+ and Ni2+ into these membranes, their affinity and selectivity towards particular gases may be altered. To promote the dispersion of metal ions within the

  13. 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.

  14. The effect of hydrogen peroxide concentration on metal ion release from dental casting alloys.

    Science.gov (United States)

    Al-Salehi, S K; Hatton, P V; Johnson, A; Cox, A G; McLeod, C

    2008-04-01

    There are concerns that tooth bleaching agents may adversely affect dental materials. The aim of this study was to test the hypothesis that increasing concentrations of hydrogen peroxide (HP) are more effective than water at increasing metal ion release from two typical dental casting alloys during bleaching. Discs (n = 28 for each alloy) were prepared by casting and heat treated to simulate a typical porcelain-firing cycle. Discs (n = 7) of each alloy were immersed in either 0%, 3%, 10% or 30% (w/v) HP solutions for 24 h at 37 degrees C. Samples were taken for metal ion release determination using inductively coupled plasma-mass spectrometry and the data analysed using a two-way anova followed by a one-way anova. The surface roughness of each disc was measured using a Talysurf contact profilometer before and after bleaching and the data analysed using a paired t-test. With the exception of gold, the differences in metal ion concentration after treatment with 0% (control) and each of 3%, 10% and 30% HP (w/v) were statistically significant (P 0.05) Exposure of the two dental casting alloys to HP solutions increased metal ion release of all the elements except gold.

  15. Cooperative Effect of a Metal Ion and Hydrogen Bonds on Phosphodiester Cleavage in Acetonitrile

    National Research Council Canada - National Science Library

    Kondo, Shin-ichi; Sakuno, Yuichi; Yokoyama, Takashi; Yano, Yumihiko

    2001-01-01

    Cleavage of an activated phosphodiester by Zn(NO3)2·6H2O was accelerated (9 × 103-fold) by cooperative effect of a metal ion and hydrogen bonds in the presence of a bismelamine derivative bearing a 2,2...

  16. removal of heavy metal ions from aqueous solution using rice husks ...

    African Journals Online (AJOL)

    User

    ABSTRACT. This study reports on the preparation and characterization of rice husks-based adsorbents and their application in the removal of heavy metal ions from aqueous solution. Three different adsorbents were developed: rice husks ash (RHA), rice husks ash-derived silica (RHS) and triaminopropyl-silica hybrid ...

  17. Biosorption of Heavy Metal Ions from Aqueous Solutions Using a Biomaterial

    Directory of Open Access Journals (Sweden)

    Innocent OBOH

    2009-07-01

    Full Text Available An increase in population initiating rapid industrialization was found to consequently increase the effluents and domestic wastewater into the aquatic ecosystem. Heavy metals are major toxicants found in industrial wastewaters; they may adversely affect the biological treatment of wastewater. Conventional methods for the removal of heavy metals from waste waters are often cost prohibitive hence, there is a need for cheap methods for effluent treatment. The residual metallic ion concentrations were determined using an Atomic Absorption Spectrophotometer (AAS. The results obtained after contacting for 120 minutes showed that Neem leaves achieved the percent removal of 76.8, 67.5, 58.4 and 41.45 for Cu2+, Ni2+, Zn2+ and Pb2+ ions respectively. The percent removal of Ni2+ ions was 68.75 with an effective dose of 1.0 g of Neem leaves (bioadsorbent. The ability of Neem leaves to absorb metal ions as shown from the results can be used for the development of an efficient, clean and cheap technology for effluent treatment.

  18. Ion dynamics in laser ablation plumes from selected metals at 355 nm

    DEFF Research Database (Denmark)

    Thestrup Nielsen, Birgitte; Christensen, Bo Toftmann; Schou, Jørgen

    2002-01-01

    The dynamics of ions in a laser ablation plume from a number of metals irradiated by a ns-second pulse at 355 nm has been studied. The time-of-flight signals peak at flight times corresponding to velocities between 30 and 10 km/s with decreasing values for increasing atomic masses. The angular...

  19. Metal-ion complexes of functionalised 1,10-Phenanthrolines as hydrolytic synzymes

    NARCIS (Netherlands)

    Weijnen, J.G.J.

    1993-01-01

    In this thesis metal-ion complexes of functionalised 1,10-phenanthroline derivatives have been studied as model systems for hydrolytic metallo-enzymes. Amphiphilic metallo- complexes incorporated into micelles or vesicles and water-soluble complexes in pure aqueous buffer solutions, have

  20. The structure of a nucleolytic ribozyme that employs a catalytic metal ion.

    Science.gov (United States)

    Liu, Yijin; Wilson, Timothy J; Lilley, David M J

    2017-05-01

    The TS ribozyme (originally called "twister sister") is a catalytic RNA. We present a crystal structure of the ribozyme in a pre-reactive conformation. Two co-axial helical stacks are organized by a three-way junction and two tertiary contacts. Five divalent metal ions are directly coordinated to RNA ligands, making important contributions to the RNA architecture. The scissile phosphate lies in a quasihelical loop region that is organized by a network of hydrogen bonding. A divalent metal ion is directly bound to the nucleobase 5' to the scissile phosphate, with an inner-sphere water molecule positioned to interact with the O2' nucleophile. The rate of ribozyme cleavage correlated in a log-linear manner with divalent metal ion pKa, consistent with proton transfer in the transition state, and we propose that the bound metal ion is a likely general base for the cleavage reaction. Our data indicate that the TS ribozyme functions predominantly as a metalloenzyme.

  1. Interactions between humic acid and hematite and their effects on metal ion speciation

    NARCIS (Netherlands)

    Vermeer, A.W.P.

    1996-01-01


    The impact of toxic chemicals (like metal ions) on the environment is a phenomenon that has been recognised as a mayor problem over the last decades. The speciation of these chemicals determines whether or not a contaminated site has to be regarded as dangerous. The fate of the

  2. Effect of metal ion concentration on the biosorption of Pb2+ and ...

    African Journals Online (AJOL)

    The influence of initial metal ion concentration of the batch sorption of Pb2+ and Cd2+ onto a low-cost biosorbent was investigated. The experimental results were analysed in terms of Langmuir and Freundlich isotherms. According to the evaluation using Langmuir equation, the monolayer sorption capacity obtained were ...

  3. Functionalized Ionic Microgel Sensor Array for Colorimetric Detection and Discrimination of Metal Ions.

    Science.gov (United States)

    Zhou, Xianjing; Nie, Jingjing; Du, Binyang

    2017-06-21

    A functional ionic microgel sensor array was developed by using 1-(2-pyridinylazo)-2-naphthaleno (PAN)- and bromothymol blue (BTB)-functionalized ionic microgels, which were designed and synthesized by quaternization reaction and anion-exchange reaction, respectively. The PAN microgels (PAN-MG) and BTB microgels (BTB-MG) were spherical in shape with a narrow size distribution and exhibited characteristic colors in aqueous solution in the presence of various trace-metal ions, which could be visually distinguished by the naked eye. Such microgels could be used for the colorimetric detection of various metal ions in aqueous solution at submicromolar levels, which were lower than the U.S. Environmental Protection Agency standard for the safety limit of metal ions in drinking water. A total of 10 species of metal ions in aqueous solution, Ba 2+ , Cr 3+ , Mn 2+ , Pb 2+ , Fe 3+ , Co 2+ , Zn 2+ , Ni 2+ , Cu 2+ , and Al 3+ , were successfully discriminated by the as-constructed microgel sensor array combined with discriminant analysis, agglomerative hierarchical clustering, and leave-one-out cross-validation analysis.

  4. Removal of textile dyes and metallic ions using polyelectrolytes and macroelectrolytes containing sulfonic acid groups.

    Science.gov (United States)

    Caldera Villalobos, M; Peláez Cid, A A; Herrera González, Ana M

    2016-07-15

    This work reports the removal of textile dyes and metallic ions by means of adsorption and coagulation-flocculation using two polyelectrolytes and two macroelectrolytes containing sulfonic acid groups. The adsorption of textile dyes was studied in aqueous solutions containing cationic dyes and in wastewater containing a vat dye. Also, removal of vat and naphthol dyes was studied using the process of coagulation-flocculation. The results show these materials possess elevated adsorption capacity, and they accomplished removal rates above 97% in aqueous solutions. The removal of the vat dye improved the quality of the wastewater notably, and an uncolored effluent was obtained at the end of the treatment. The treatment using adsorption decreased the values for coloration, conductivity, suspended solids, and pH. The removal of vat and naphthol dyes by means of coagulation-flocculation was studied as well, and removal rates of 90% were obtained. The polyelectrolytes and macroelectrolytes also proved effective in the adsorption of metallic ions in wastewater. The treatment using adsorption accomplished high removal rates of metallic ions, and it showed greater selectivity towards Cu(2+), Fe(3+) and Pb(2+). A decrease in the content of solids as well as the values for COD and conductivity was observed in the wastewater as well. The analyses of FT-IR indicated that cationic dyes and metallic ions were chemisorbed by means of ionic exchange. Copyright © 2016 Elsevier Ltd. All rights reserved.

  5. 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.

  6. Polarographic Determination of Composition and Thermodynamic Stability Constant of a Complex Metal Ion.

    Science.gov (United States)

    Marin, Dolores; Mendicuti, Francisco

    1988-01-01

    Describes a laboratory experiment designed to encourage laboratory cooperation among individual undergraduate students or groups. Notes each student contributes results individually and the exchange of data is essential to obtain final results. Uses the polarographic method for determining complex metal ions. (MVL)

  7. Multiheteromacrocycles that Complex Metal Ions. Fourth Progress Report, 1 May 1977 -- 30 April 1978

    Science.gov (United States)

    Cram, D. J.

    1978-01-15

    Results are reported in a program to design, synthesize, and evaluate polycyclic host organic compounds for their abilities to complex and lipophilize guest metal ions. Work during the reporting period was devoted to synthesis and study of cyclohexametaphenylenes and cyclic phosphine oxides. (JRD)

  8. The connection between metal ion affinity and ligand affinity in integrin I domains

    DEFF Research Database (Denmark)

    Vorup-Jensen, Thomas; Waldron, TT; Astrof, N

    2007-01-01

    Integrins are cell-surface heterodimeric proteins that mediate cell-cell, cell-matrix, and cell-pathogen interactions. Half of the known integrin alpha subunits contain inserted domains (I domains) that coordinate ligand through a metal ion. Although the importance of conformational changes withi...

  9. No Giant Two-Ion Anisotropy in the Heavy-Rare-Earth Metals

    DEFF Research Database (Denmark)

    Lindgård, Per-Anker

    1976-01-01

    A new Bose-operator expansion of tensor operators is applied to the heavy-rare-earth metals. The Er data for the cone phase have been analyzed successfully with single-ion anisotropy and isotropic exchange interaction. The Tb data can be understood on the same basis. The previously found large two...

  10. Metal ion-mediated agonism and agonist enhancement in melanocortin MC1 and MC4 receptors

    DEFF Research Database (Denmark)

    Holst, Birgitte; Elling, Christian E; Schwartz, Thue W

    2002-01-01

    -melanocortin stimulating hormone (alpha-MSH) in the MC1 and MC4 receptors, respectively. In the presence of peptide agonist, Zn(II) acted as an enhancer on both receptors, because it shifted the dose-response curves to the left: most pronounced was a 6-fold increase in alpha-MSH potency on the MC1 receptor. The effect...... of the metal ion appeared to be additive, because the maximal cAMP response for alpha-MSH in the presence of Zn(II) was 60% above the maximal response for the peptide alone. The affinity of Zn(II) could be increased through binding of the metal ion in complex with small hydrophobic chelators. The binding...... in the MC1 receptor. Metal ion-chelator complexes having antagonistic properties were also found. An initial attempt to map the metal-ion binding site in the MC1 receptor indicated that Cys(271) in extracellular loop 3 and possibly Asp(119) at the extracellular end of TM-III, which are both conserved among...

  11. Metal ion site engineering indicates a global toggle switch model for seven-transmembrane receptor activation

    DEFF Research Database (Denmark)

    Elling, Christian E; Frimurer, Thomas M; Gerlach, Lars-Ole

    2006-01-01

    for monoamine binding in TM-III, was used as the starting point to engineer activating metal ion sites between the extracellular segments of the beta2-adrenergic receptor. Cu(II) and Zn(II) alone and in complex with aromatic chelators acted as potent (EC50 decreased to 0.5 microm) and efficacious agonists...

  12. Recovery process for phenolic compounds from coal-derived oils by ions of soluble metal salts

    Energy Technology Data Exchange (ETDEWEB)

    Yizhang Ge; Hong Jin [Hefei Institute of Coal, Hefei (China)

    1996-11-01

    Phenolic compounds in a fraction (170-210{degree}C) of multistage rotary furnace coal tar pyrolysed from Tian Zhu brown coal at 550{degree}C were efficiently recovered by precipitation using ions of soluble metal salts as precipitant. The method overcomes the defects of the extraction method using 10 wt% NaOH solution. 8 refs., 2 figs., 3 tabs.

  13. Coloring a Superabsorbent Polymer with Metal Ions: An Undergraduate Chemistry Experiment

    Science.gov (United States)

    Yaung, Jing-Fun; Chen, Yueh-Huey

    2009-01-01

    A novel undergraduate chemistry experiment involving superabsorbent polymers commonly used in diapers and other personal care products is described. Students observe the removal of divalent transition-metal ions from aqueous solutions by the polymers. With the procedures provided, students are able to color the superabsorbent polymers with metal…

  14. Preparation and characterization of gum karaya hydrogel nanocomposite flocculant for metal ions removal from mine effluents

    CSIR Research Space (South Africa)

    Fosso-Kankeu, E

    2016-02-01

    Full Text Available This research paper reports the removal of heavy metal ions from mine effluents using the gum karaya (GK)-grafted poly(acrylamide-co-acrylic acid) incorporated iron oxide magnetic nanoparticles (Fe3O4 MNPs) hydrogel nanocomposite [i.e., GK...

  15. Surface Modification of Polypropylene Membrane Using Biopolymers with Potential Applications for Metal Ion Removal

    Directory of Open Access Journals (Sweden)

    Omar Alberto Hernández-Aguirre

    2016-01-01

    Full Text Available This work aims to present the modification of polypropylene (PP membranes using three different biopolymers, chitosan (CHI, potato starch (PS, and cellulose (CEL, in order to obtain three new materials. The modified membranes may be degraded easier than polypropylene ones and could be used as selective membranes for metal ions removal, among other applications. For this purpose, the UV energy induced graft copolymerization reaction among polypropylene membrane, acrylic acid, benzophenone (as photoinitiator, and the biopolymer (CHI, PS, or CEL was conducted. The results of FT-IR-ATR, XRD, TGA, DSC, SEM, BET, and AFM analyses and mechanical properties clearly indicate the successful modification of the membrane surface. The change of surface wettability was monitored by contact angle. The grafting reaction depends on natural polymer, reaction time, and concentration. In order to prove the potential application of the modified membranes, a preliminary study of sorption of metal ion was carried out. For this purpose, the PP-CHI membrane was chosen because of the high hydrophilicity, proportionate to -OH and NH2; these groups could act as ligands of metal ions, provoking the interaction between PP-CHI and M+ (PP-CHI-M+ and therefore the metal ion removal from water.

  16. Bio-extraction of metal ions from laterite ore by Penicillium ...

    African Journals Online (AJOL)

    Administrator

    2011-09-19

    Sep 19, 2011 ... 2008). Microorganisms like heterotrophs require carbon as an energy source, and this requirement can be fulfilled by using organic wastes. Acidolysis is the principal mechanism in bioleaching of metal ions by fungus. The fungus produces organic acids such as citric, oxalic, malic and gluconic acids during ...

  17. Effect of metal ions on the growth and metabolites production of ...

    African Journals Online (AJOL)

    The effects of several metal ions on the cell growth, production of polysaccharides by Ganoderma lucidum in submerged fermentation were studied. The results showed that 50 ppm Se2+ and 25 ppm Se2+ was identified to be the most favorable for biomass (11.103 ± 0.6 g/l ) and polysaccharide production (IPS and EPS ...

  18. Metal ion coordination inR'andT'state hybrid hemoglobins as ...

    Indian Academy of Sciences (India)

    It is found that there exists a correlation between conformational change and metal ion environment, not only at the extreme R and T states but also the intermediate ... 600 036, India; Molecular Dynamics Section, National Institute on Aging, National Institutes of Health, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA ...

  19. Removal of heavy metal ions from wastewaters using dendrimer-functionalized multi-walled carbon nanotubes.

    Science.gov (United States)

    Iannazzo, Daniela; Pistone, Alessandro; Ziccarelli, Ida; Espro, Claudia; Galvagno, Signorino; Giofré, Salvatore V; Romeo, Roberto; Cicero, Nicola; Bua, Giuseppe D; Lanza, Giuseppe; Legnani, Laura; Chiacchio, Maria A

    2017-06-01

    Dendrimer-functionalized multi-walled carbon nanotubes (MWCNT) for heavy metal ion removal from wastewaters were developed. Triazole dendrimers (TD) were built directly onto the carbon nanotube surface by successive click chemistry reactions affording the zero- and first-generation dendrimer-functionalized MWCNT (MWCNT-TD1 and MWCNT-TD2). The Moedritzer-Irani reaction carried out on the amino groups present on the MWCNT-TD2 sample gave the corresponding α-aminophosphonate nanosystem MWCNT-TD2P. Both MWCNT-TD2 and MWCNT-TD2P nanosystems have been characterized by physical, chemical, and morphological analyses. Their chelating abilities towards the toxic metal ions Pb2+, Hg2+, and Ni2+ and the harmless Ca2+ ion have been experimentally evaluated in the two different sets of experiments and at the salt concentrations of 1 mg/mL or 1 μg/mL by inductively coupled plasma mass spectrometry (ICP-MS). The results of these studies pointed out the interesting chelating behavior for the phosphonated nanosystem towards the Hg2+ ion. The complexation mode of the best chelating system MWCNT-TD2P with mercury was investigated through density functional theory (DFT) calculations, suggesting a chelation mechanism involving the two oxygen atoms of the phosphate group. The synthesized dendrimers, supported on the multi-walled carbon nanotubes, have shown the potential to be used for the selective toxic metal ion removal and recovery.

  20. Method and apparatus for ion sequestration and a nanostructured metal phosphate

    Science.gov (United States)

    Mattigod, Shas V [Richland, WA; Fryxell, Glen E [Kennewic, WA; Li, Xiaohong [Richland, WA; Parker, Kent E [Kennewick, WA; Wellman, Dawn M [West Richland, WA

    2010-04-06

    A nanostructured substance, a process for sequestration of ionic waste, and an ion-sequestration apparatus are disclosed in the specification. The nanostructured substance can comprise a Lewis acid transition metal bound to a phosphate, wherein the phosphate comprises a primary structural component of the substance and the Lewis acid transition metal is a reducing agent. The nanostructured substance has a Brunner-Emmet-Teller (BET) surface area greater than or equal to approximately 100 m.sup.2/g, and a distribution coefficient for an analyte, K.sub.d, greater than or equal to approximately 5000 ml/g. The process can comprise contacting a fluid and a nanostructured metal phosphate. The apparatus can comprise a vessel and a nanostructured metal phosphate. The vessel defines a volume wherein a fluid contacts the nanostructured metal phosphate.

  1. Interaction between alpha-synuclein and metal ions, still looking for a role in the pathogenesis of Parkinson's disease.

    Science.gov (United States)

    Bisaglia, Marco; Tessari, Isabella; Mammi, Stefano; Bubacco, Luigi

    2009-01-01

    The most recent literature on the interaction between alpha-synuclein in its several aggregation states and metal ions is discussed. This analysis shows two major types of interactions. Binding sites are present in the C-terminal region, and similar, low affinity (in the millimolar range) is exhibited toward many different metal ions, including copper and iron. A more complex scenario emerges for these latter metal ions, which are also able to coordinate with high affinity (in the micromolar range) to the N-terminal region of alpha-synuclein. Moreover, these redox-active metal ions may induce chemical modifications on the protein in vitro and in the reducing intracellular environment, and these modifications might be relevant for the aggregation properties of alpha-synuclein. Finally, an attempt is made to contextualize the interaction between alpha-synuclein and these metal ions in the framework of the elusive and multifactorial pathogenesis of Parkinson's disease.

  2. Asparagus cochinchinensis Extract Alleviates Metal Ion-Induced Gut Injury in Drosophila: An In Silico Analysis of Potential Active Constituents

    Directory of Open Access Journals (Sweden)

    Weiyu Zhang

    2016-01-01

    Full Text Available Metal ions and sulfate are components of atmospheric pollutants that have diverse ways of entering the human body. We used Drosophila as a model to investigate the effect of Asparagus cochinchinensis (A. cochinchinensis extracts on the gut and characterized gut homeostasis following the ingestion of metal ions (copper, zinc, and aluminum. In this study, we found that the aqueous A. cochinchinensis extract increased the survival rate, decreased epithelial cell death, and attenuated metal ion-induced gut morphological changes in flies following chronic exposure to metal ions. In addition, we screened out, by network pharmacology, six natural products (NPs that could serve as putative active components of A. cochinchinensis that prevented gut injury. Altogether, the results of our study provide evidence that A. cochinchinensis might be an effective phytomedicine for the treatment of metal ion-induced gut injury.

  3. Interaction of different metal ions with carboxylic acid group: a quantitative study.

    Science.gov (United States)

    Bala, Tanushree; Prasad, B L V; Sastry, Murali; Kahaly, Mousumi Upadhyay; Waghmare, Umesh V

    2007-07-19

    The binding strength of the carboxylic acid group (-COOH) with different divalent metal ions displays considerable variation in arachidic acid (AA) thin films. It is considered that in AA thin films the metal ions straddle the hydrophilic regions of the stacked bilayers of AA molecules via formation of carboxylates. In this study first the uptake of different divalent cations in films of AA is estimated by atomic absorption spectroscopy (AAS). Through the amount of cation uptake, it is found that the strength of binding of different cations varies as Ca2+>Co2+>Pb2+>Cd2+. Variation in the binding strength of different ions is also manifested in experiments where AA thin films are exposed to metal ion mixtures. The higher binding strength of AA with certain metal ions when exposed individually, as well as the preference over the other metal ions when exposed to mixtures, reveal some interesting deviation from the expected behavior based on considerations of ionic radii. For example, Pb2+ is always found to bind to AA much more strongly than Cd2+ even though the latter has smaller ionic radius, indicating that other factors also play an important role in governing the binding strength trends apart from the effects of ionic radii. Then, to get a more meaningful knowledge regarding the binding capability, first-principles calculations based on density functional theory have been applied to study the interaction of different cations with the simplest carboxylic acid, acetic acid, that can result in formation of metal diacetates. Their electronic and molecular structures, cohesive energies, and stiffness of the local potential energy well at the cation (M) site are determined and attempts are made to understand the diversity in geometry and the properties of binding of different metal ions with -COOH group. We find that the calculated M-O bond energies depend sensitively on the chemistry of M atom and follow the experimentally observed trends quite accurately. The trends

  4. Research on Multi-Ion Interactions and Defects in Metals.

    Science.gov (United States)

    1982-07-09

    Reference 18; based on Sha %% data. fcc intrinsic-fault energy, while at the same time "Rderence 18; based on Animalu data. reducing the predicted values of...the de- tReference 19; based on Sha % 4ata. ’Reference 9; based on Harrson’s pseudopotential. sired characteristic is shown in Fig. 6. This ID. H...SCREENING EFFECT IN THE THEORY OF ELECTRIC FIELD GRADIENTS IN DILUTE ALLOYS OF SIMPLE METALS R.I, BIASSNIR .S)t l hvest Resa ’ra’ Inistitut’ San .4nt

  5. Linking Metal Ions via Inorganic Click (iClick) Reactions

    Energy Technology Data Exchange (ETDEWEB)

    Veige, Adam [Univ. of Florida, Gainesville, FL (United States)

    2015-11-17

    This final report discusses the major objectives of the project, a discussion of the objectives achieved, a discussion of the objectives that failed, and finally, a discussion of future directions given the new knowledge obtained. This one-year seed project (with one year no-cost extension) contained three objectives: A) Expand the scope of iClick synthesis beyond AuI/AuI reactions. B) Elucidate a CuI-catalyzed iClick reaction. C) Synthesize and characterize tri- and tetra-metallic complexes as models for metallopolymers. Objectives A and C were achieved, whereas only parts of objective B were achieved.

  6. Lead and other metal ions in United States precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Lazrus, A.L.; Lorange, E.; Lodge, J.P. Jr.

    1970-01-01

    Atmospheric precipitation samples collected by a nationwide network of 32 stations throughout the United States were analyzed for lead, zinc, copper, iron, manganese, and nickel by atomic absorption. Values for each station averaged over approximately six months during 1966 and 1967 indicate human activity as the primary source of these materials in atmospheric precipitation. The concentration of lead in precipitation was found to be correlated with the amount of gasoline consumed in the area in which the sample was collected. The overall mean concentrations of the metals in precipitation are compared with analogous values in surface water supplies.

  7. Development of an Electrochemical Metal-Ion Biosensor Using Self-Assembled Peptide Nanofibrils

    DEFF Research Database (Denmark)

    Viguier, Bruno; Zor, Kinga; Kasotakis, Emmanouil

    2011-01-01

    This article describes the combination of self-assembled peptide nanofibrils with metal electrodes for the development of an electrochemical metal-ion biosensor. The biological nanofibrils were immobilized on gold electrodes and used as biorecognition elements for the complexation with copper ions....... These nanofibrils were obtained under aqueous conditions, at room temperature and outside the clean room. The functionalized gold electrode was evaluated by cyclic voltammetry, impedance spectroscopy, energy dispersive X-ray and atomic force microscopy. The obtained results displayed a layer of nanofibrils able...... to complex with copper ions in solution. The response of the obtained biosensor was linear up to 50 µM copper and presented a sensitivity of 0.68 µAcm-2µM-1. Moreover, the fabricated sensor could be regenerated to a copper-free state allowing its re-utilization....

  8. Positive ions of the first- and second-row transition metal hydrides

    Science.gov (United States)

    Pettersson, Lars G. M.; Bauschlicher, Charles W., Jr.; Langhoff, Stephen R.; Partridge, Harry

    1987-01-01

    Theoretical dissociation energies for the first- and second-row transition metal hydride positive ions are critically compared against recent experimental values obtained from ion beam reactive scattering methods. Theoretical spectroscopic parameters and dipole moments are presented for the ground and several low-lying excited states. The calculations employ large Gaussian basis sets and account for electron correlation using the single-reference single- and double-excitation configuration interaction and coupled-pair-functional methods. The Darwin and mass-velocity contributions to the relativistic energy are included in the all-electron calculations on the first-row systems using first-order perturbation theory, and in the second-row systems using the Hay and Wadt relativistic effective core potentials. The theoretical D(0) values for the second-row transition metal hydride positive ions should provide a critical measure of the experimental values, which are not as refined as many of those in the first transition row.

  9. Synthesis of diethylaminoethyl dextran hydrogel and its heavy metal ion adsorption characteristics.

    Science.gov (United States)

    Demirbilek, Celile; Dinç, Cemile Özdemir

    2012-10-01

    Epichlorohydrin-crosslinked diethylaminoethyl dextran (DEAE-D/ECH) hydrogel was synthesized by intermolecular side-chain reaction of DEAE-D hydroxyl groups with monomeric crosslinking agent, ECH. Swelling ability, adsorption capacity and metal removal of the hydrogel were profoundly determined and some structural parameters for the hydrogel such as volume of non-swollen gel, percentages of gellation, swelling ratio and equilibrium water content were evaluated in this study. The ability of removing heavy metal ions from Orontes River by the synthesized hydrogel, thoroughly characterized by photometric spectrometer and the adsorption characteristics of metal ions, was investigated as well as surface morphologies of the hydrogel before and after metal adsorption were examined by SEM. Structure of DEAE-D/ECH gel was analyzed by FTIR, TGA, and DSC. Gellation point of binary system reaction between DEAE-D and ECH was determined via monitoring viscosity changes during reaction. The order of affinity based on amount of metal ion uptake was found as follows: Zn(2+)>Mn(2+)>Pb(2+)>Cd(2+). Copyright © 2012 Elsevier Ltd. All rights reserved.

  10. Metal ion leachates and the physico-chemical stability of biotherapeutic drug products.

    Science.gov (United States)

    Kumar, Sandeep; Zhou, Shuxia; Singh, Satish K

    2014-01-01

    Metal ions that leach into biotherapeutic drug product solution during manufacturing and storage, result in contamination that can cause physico-chemical degradation of the active molecule. In this review, we describe various mechanisms by which metal ion leachates can interact with therapeutic proteins and antibodies. Site-specific modifications due to metal catalyzed oxidation (MCO) of the therapeutic proteins cause them to become destabilized and potentially increasingly aggregation prone. We have examined the molecular sequences and structures for three case studies, human relaxin (hRlx), human growth hormone (hGH) and an IgG2 mAb to rationalize the experimental findings related to their MCO. The analysis indicates that metal-binding sites lie in close spatial proximities to predicted aggregation prone regions in these molecules. From the perspective of pharmaceutical development of biotherapeutic drugs, this link between molecular origins of MCO and subsequent aggregation is undesirable. This article further suggests molecular design strategies involving disruption of APRs that may also help mitigate the impact of metal ion leachates on biotherapeutic drug products as well as improving their solubility.

  11. Nanostructured Block Polymer Membranes as High Capacity Adsorbers for the Capture of Metal Ions from Water

    Science.gov (United States)

    Boudouris, Bryan; Weidman, Jacob; Mulvenna, Ryan; Phillip, William

    The efficient removal of metal ions from aqueous streams is of significant import in applications ranging from industrial waste treatment to the purification of drinking water. An emerging paradigm associated with this separation is one that utilizes membrane adsorbers as a means by which to bind metal salt contaminants. Here, we demonstrate that the casting of an A-B-C triblock polymer using the self-assembly and non-solvent induced phase separation (SNIPS) methodology results in a nanoporous membrane geometry. The nature of the triblock polymer affords an extremely high density of binding sites within the membrane. As such, we demonstrate that the membranes with binding capacities equal to that of state-of-the-art packed bed columns. Moreover, because the affinity of the C moiety can be tuned, highly selective binding events can occur based solely on the chemistry of the block polymer and the metal ions in solution (i.e., in a manner that is independent of the size of the metal ions). Due to these combined facts, these membranes efficiently remove heavy metal (e.g., lead- and cadmium-based) salts from contaminated water streams with greater than 95% efficiency. Finally, we show that the membranes can be regenerated through a simple treatment in order to provide long-lasting adsorber systems as well. Thus, it is anticipated that these nanostructured triblock polymer membranes are a platform by which to obtain next-generation water purification processes.

  12. Removal of heavy metal ions from aqueous solution by zeolite synthesized from fly ash.

    Science.gov (United States)

    He, Kuang; Chen, Yuancai; Tang, Zhenghua; Hu, Yongyou

    2016-02-01

    Zeolite was synthesized from coal fly ash by a fusion method and was used for the removal of heavy metal ions (Pb(2+), Cd(2+), Cu(2+), Ni(2+), and Mn(2+)) in aqueous solutions. Batch method was employed to study the influential parameters such as adsorbent dosage, pH, and coexisting cations. Adsorption isotherms and kinetics studies were carried out in single-heavy and multiheavy metal systems, respectively. The Langmuir isotherm model fitted to the equilibrium data better than the Freundlich model did, and the kinetics of the adsorption were well described by the pseudo-second-order model, except for Cd(2+) and Ni(2+) ions which were fitted for the pseudo-first-order model in the multiheavy metal system. The maximum adsorption capacity and the distribution coefficients exhibited the same sequence for Pb(2+) > Cu(2+) > Cd(2+) > Ni(2+) > Mn(2+) in both single- and multiheavy metal systems. In the end, the adsorption capacity of zeolite was tested using industrial wastewaters and the results demonstrated that zeolite could be used as an alternative adsorbent for the removal of heavy metal ions from industrial wastewater.

  13. Synthesis of ethylenediamine modified chitosan and evaluation for removal of divalent metal ions.

    Science.gov (United States)

    Chethan, P D; Vishalakshi, B

    2013-09-12

    Selective modification of chitosan has been achieved by incorporating ethylene-1,2-diamine molecule in a regioselective manner using N-phthaloylchitosan and chloro-6-deoxy N-phthaloylchitosan as precursors. The present modification results in additional nitrogen centres which function as potential binding sites during adsorption of metal ions. The derivative ethylene-1,2-diamine-6-deoxy-chitosan and its pthaloylated precursor have been evaluated for divalent metal ion removal. The former is found to have higher capacity for adsorption due to the presence of additional NH₂ group. The samples exhibited highest affinity for Cu and least for Zn. About 80% of the adsorbed metal ions could be stripped in a solution of pH 1.2. The interaction between acidic metal centres and basic nitrogen centres on surface of the adsorbent appears to govern adsorption. Intrachain and interchain co-ordinate bonding involving NH and NH₂ groups is proposed to be the mechanism of formation of metal-adsorbent complex. The adsorption process is described by Langmuir model. Copyright © 2013 Elsevier Ltd. All rights reserved.

  14. Effect of carbon ion implantation on the tribology of metal-on-metal bearings for artificial joints.

    Science.gov (United States)

    Koseki, Hironobu; Tomita, Masato; Yonekura, Akihiko; Higuchi, Takashi; Sunagawa, Sinya; Baba, Koumei; Osaki, Makoto

    2017-01-01

    Metal-on-metal (MoM) bearings have become popular due to a major advantage over metal-on-polymer bearings for total hip arthroplasty in that the larger femoral head and hydrodynamic lubrication of the former reduce the rate of wear. However, concerns remain regarding adverse reactions to metal debris including metallosis caused by metal wear generated at the taper-head interface and another modular junction. Our group has hypothesized that carbon ion implantation (CII) may improve metal wear properties. The purpose of this study was to investigate the wear properties and friction coefficients of CII surfaces with an aim to ultimately apply these surfaces to MoM bearings in artificial joints. CII was applied to cobalt-chromium-molybdenum (Co-Cr-Mo) alloy substrates by plasma source ion implantation. The substrates were characterized using scanning electron microscopy and a 3D measuring laser microscope. Sliding contact tests were performed with a simple geometry pin-on-plate wear tester at a load of 2.5 N, a calculated contact pressure of 38.5 MPa (max: 57.8 MPa), a reciprocating velocity of 30 mm/s, a stroke length of 60 mm, and a reciprocating cycle count of 172,800 cycles. The surfaces of the CII substrates were generally featureless with a smooth surface topography at the same level as untreated Co-Cr-Mo alloy. Compared to the untreated Co-Cr-Mo alloy, the CII-treated bearings had lower friction coefficients, higher resistance to catastrophic damage, and prevented the adhesion of wear debris. The results of this study suggest that the CII surface stabilizes the wear status due to the low friction coefficient and low infiltration of partner materials, and these properties also prevent the adhesion of wear debris and inhibit excessive wear. Carbon is considered to be biologically inert; therefore, CII is anticipated to be applicable to the bearing surfaces of MoM prostheses.

  15. Facile synthesis of nanostructured transition metal oxides as electrodes for Li-ion batteries

    Science.gov (United States)

    Opra, Denis P.; Gnedenkov, Sergey V.; Sokolov, Alexander A.; Minaev, Alexander N.; Kuryavyi, Valery G.; Sinebryukhov, Sergey L.

    2017-09-01

    At all times, energy storage is one of the greatest scientific challenge. Recently, Li-ion batteries are under special attention due to high working voltage, long cycle life, low self-discharge, reliability, no-memory effect. However, commercial LIBs usage in medium- and large-scale energy storage are limited by the capacity of lithiated metal oxide cathode and unsafety of graphite anode at high-rate charge. In this way, new electrode materials with higher electrochemical performance should be designed to satisfy a requirement in both energy and power. As it known, nanostructured transition metal oxides are promising electrode materials because of their elevated specific capacity and high potential vs. Li/Li+. In this work, the perspective of an original facile technique of pulsed high-voltage plasma discharge in synthesis of nanostructured transition metal oxides as electrodes for lithium-ion batteries has been demonstrated.

  16. Advanced material and approach for metal ions removal from aqueous solutions

    Science.gov (United States)

    Turhanen, Petri A.; Vepsäläinen, Jouko J.; Peräniemi, Sirpa

    2015-03-01

    A Novel approach to remove metals from aqueous solutions has been developed. The method is based on a resin free, solid, non-toxic, microcrystalline bisphosphonate material, which has very low solubility in water (59 mg/l to ion free Milli-Q water and 13 mg/l to 3.5% NaCl solution). The material has been produced almost quantitatively on a 1 kg scale (it has been prepared also on a pilot scale, ca. 7 kg) and tested successfully for its ability to collect metal cations from different sources, such as ground water and mining process waters. Not only was this material highly efficient at collecting several metal ions out of solution it also proved to be regenerable and reusable over a number of adsorption/desorption, which is crucial for environmental friendliness. This material has several advantages compared to the currently used approaches, such as no need for any precipitation step.

  17. Polydopamine-mediated surface-functionalization of graphene oxide for heavy metal ions removal

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Zhihui [Nano-Bionics Division and i-LAB, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123 (China); University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing 100049 (China); Zhang, Feng; Wang, Dong; Liu, Xia [Nano-Bionics Division and i-LAB, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123 (China); Jin, Jian, E-mail: jjin2009@sinano.ac.cn [Nano-Bionics Division and i-LAB, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123 (China)

    2015-04-15

    By utilizing polydopamine (PD) nano-thick interlayer as mediator, polyethylenimine (PEI) brushes with abundant amine groups were grafted onto the surface of PD coated graphene oxide (GO) uniformly via a Michael-Addition reaction and produced a PEI–PD/GO composite nanosheets. The PEI–PD/GO composite exhibited an improved performance for adsorption of heavy metal ions as compared to PEI-coated GO and pure GO. The adsorption capacities for Cu{sup 2+}, Cd{sup 2+}, Pb{sup 2+}, Hg{sup 2+} are up to 87, 106, 197, and 110 mg/g, respectively. To further make the GO based composite operable, PEI–PD/RGO aerogel was prepared through hydrothermal and achieved a high surface area up to 373 m{sup 2}/g. Although the adsorption capacity of PEI–PD/RGO aerogel for heavy metal ions decreases a little as compared to PEI–PD/GO composite dispersion (38, 32, 95, 113 mg/g corresponding to Cu{sup 2+}, Cd{sup 2+}, Pb{sup 2+}, and Hg{sup 2+}, respectively), it could be recycled several times in a simple way by releasing adsorbed metal ions, indicating its potential application for cleaning wastewater. - Graphical abstract: Polyethylenimine (PEI) brushes were grafted onto the surface of graphene oxide (GO) uniformly via a Michael-Addition reaction between the PEI and polydopamine interlayer coated on GO surface. The PEI–PD/GO composite exhibited an improved performance for adsorption of heavy metal ions compared to PEI-coated GO and pure GO. - Highlights: • We prepared polyethylenimine grafted polydopamine-mediated graphene oxide composites. • Introduction of PD layer increases metal ions adsorption capacity. • PEI–PD/RGO aerogel exhibited a superior adsorption performance. • PEI–PD/RGO aerogel can be recycled several times in a simple way.

  18. A novel Schiff base: Synthesis, structural characterisation and comparative sensor studies for metal ion detections.

    Science.gov (United States)

    Köse, Muhammet; Purtas, Savas; Güngör, Seyit Ali; Ceyhan, Gökhan; Akgün, Eyup; McKee, Vickie

    2015-02-05

    A novel Schiff base ligand was synthesized by the condensation reaction of 2,6-diformylpyridine and 4-aminoantipyrine in MeOH and characterised by its melting point, elemental analysis, FT-IR, (1)H, (13)C NMR and mass spectroscopic studies. Molecular structure of the ligand was determined by single crystal X-ray diffraction technique. The electrochemical properties of the Schiff base ligand were studied in different solvents at various scan rates. Sensor ability of the Schiff base ligand was investigated by colorimetric and fluorometric methods. Visual colour change of the ligand was investigated in MeOH solvent in presence of various metal ions Na(+), Mg(2+), Al(3+), K(+), Cr(3+), Mn(2+), Fe(3+), Co(2+), Ni(2+), Cu(2+), Zn(2+), Cd(2+), Hg(2+) and Pb(2+). Upon addition of Al(3+) ion into a MeOH solution of the ligand, an orange colour developed which is detectable by naked eye. Fluorescence emission studies showed that the ligand showed single emission band at 630-665nm upon excitation at 560nm. Addition of metal ions Na(+), Mg(2+), K(+), Cr(3+), Mn(2+), Fe(3+), Co(2+), Ni(2+), Cu(2+), Zn(2+), Cd(2+), Hg(2+) and Pb(2+) (1:1M ratio) cause fluorescence quenching, however addition of Al(+3) resulted in an increase in fluorescence intensity. No significant variation was observed in the fluorescence intensity caused by Al(3+) in presence of other metal ions. Therefore, the Schiff base ligand can be used for selective detection of Al(3+) ions in the presence of the other metal ions studied. Copyright © 2014 Elsevier B.V. All rights reserved.

  19. Characterization of charge and kinetic energy distribution of ions emitted during nanosecond pulsed laser ablation of several metals

    Science.gov (United States)

    Dogar, A. H.; Ullah, S.; Qayyum, H.; Rehman, Z. U.; Qayyum, A.

    2017-09-01

    The ion flux from various metals (Al, Ti, Cu, Sn and W) ablated with 20 ns Nd:YAG laser radiation at a wavelength of 1064 nm was investigated by an ion collector operating in time-of-flight (TOF) configuration. The laser irradiance at the target was varied in the range of 1.7  ×  108-5.73  ×  108 W cm-2. Ion yield from various metals showed a linearly increasing trend with increasing laser irradiance, whereas ion yield was found to decrease with an increasing atomic mass of the target. Our results clearly indicate that ion yield is not a function of the volatility of the metal. TOF ion spectra showed at least two groups of low intensity peaks due to fast ions. The first group of ion peaks, which was present in the spectra of all five metals, was due to surface contamination. The additional fast ion structures in the spectra of Sn and W can be related to the ion acceleration due to the prompt electron emission from these high-Z metals. The ion velocity follows the anticipated inverse square root dependence on the ion mass. For the range of laser irradiance investigated here, the most probable energy of the Cu ions increases from about 100-600 eV. The fast increase in ion energy above ~3  ×  108 W cm-2 is related to the increase of the Columb part of the ion energy due to the production of multiply charged ions.

  20. Electron and ion induced electron emission from metals and insulators

    CERN Document Server

    Steinbatz, M

    2001-01-01

    gradually exposed to oxygen as an experimental probe. The experimental data are fitted with an analytical model, that is able to describe the observed kinetics. The fit parameters give absolute values of sticking probabilities and of surface reaction rates. During oxidation of aluminum and magnesium also spontaneous emission of electrons (exoelectrons) is observed. This effect is quantitatively studied for different oxygen partial pressures. The experimental data also indicate a significant influence of the surface morphology on the exoemission process. An important consequence of atomic collisions in solids is ionization leading to electron ejection from the target atoms with subsequent migration through the solid. A certain fraction of these electrons finally reaches the surface and is ejected into vacuum. A standard measurement of this phenomenon is the observation of the particle (electron, ion) induced electron emission yield g, defined as the average number of ejected electrons per incoming projectile. ...

  1. Metals Ions Removal by Polymer Membranes of Different Porosity

    Directory of Open Access Journals (Sweden)

    Katarzyna Jasiewicz

    2013-01-01

    Full Text Available The effect of the amount of pore generating agent (polyvinylpyrrolidone added to standard polymer membranes containing 18 wt.% of polyethersulfone on the physicochemical properties of the membranes and their capacity for removal of iron and copper ions from the liquid phase was studied. The membranes were obtained by the phase inversion method. The results have shown that the modification of polymer membranes by the use of different amounts of the pore forming agent in their syntheses leads to significant changes in porosity and has beneficial effect on equilibrium water content. The membranes studied were found to show different acid-base surface character, but for all membranes studied, a significant dominance of oxygen groups of acidic character was evidenced. The most effective were the membranes of the lowest content of polyvinylpyrrolidone, while the lowest values of resistance showed the membranes of the highest content of PVP, and so the ones of the greatest porosity.

  2. Polymerization effect of electrolytes on hydrogen-bonding cryoprotectants: ion-dipole interactions between metal ions and glycerol.

    Science.gov (United States)

    Weng, Lindong; Elliott, Gloria D

    2014-12-11

    Protectants which are cell membrane permeable, such as glycerol, have been used effectively in the cryopreservation field for a number of decades, for both slow cooling and vitrification applications. In the latter case, the glass transition temperature (Tg) of the vitrification composition is key to its application, dictating the ultimate storage conditions. It has been observed that the addition of some electrolytes to glycerol, such as MgCl2, could elevate the Tg of the mixture, thus potentially providing more storage condition flexibility. The microscopic mechanisms that give rise to the Tg-enhancing behavior of these electrolytes are not yet well understood. The current study focuses on molecular dynamics simulation of glycerol mixed with a variety of metal chlorides (i.e., NaCl, KCl, MgCl2, and CaCl2), covering a temperature range that spans both the liquid and glassy states. The characteristics of the ion-dipole interactions between metal cations and hydroxyl groups of glycerol were analyzed. The interruption of the original hydrogen-bonding network among glycerol molecules by the addition of ions was also investigated in the context of hydrogen-bonding quantity and lifetime. Divalent metal cations were found to significantly increase the Tg by strengthening the interacting network in the electrolyte/glycerol mixture via strong cation-dipole attractions. In contrast, monovalent cations increased the Tg insignificantly, as the cation-dipole attraction was only slightly stronger than the original hydrogen-bonding network among glycerol molecules. The precursor of crystallization of NaCl and KCl was also observed in these compositions, potentially contributing to weak Tg-enhancing ability. The Tg-enhancing mechanisms elucidated in this study suggest a structure-enhancing role for divalent ions that could be of benefit in the design of protective formulations for biopreservation purposes.

  3. Chloride ion-aided self-assembly of pseudoclathrochelate metal tris-pyrazoloximates.

    Science.gov (United States)

    Varzatskii, Oleg A; Penkova, Larysa V; Kats, Svitlana V; Dolganov, Alexander V; Vologzhanina, Anna V; Pavlov, Alexander A; Novikov, Valentin V; Bogomyakov, Artem S; Nemykin, Victor N; Voloshin, Yan Z

    2014-03-17

    Chloride ion-aided one-pot template self-assembly of a mixed pyrazoloxime ligand with phenylboronic acid on a corresponding metal(II) ion as a matrix afforded the first boron-capped zinc, cobalt, iron, and manganese pseudoclathrochelate tris-pyrazoloximates. The presence of a pseudocross-linking hydrogen-bonded chloride ion is critical for their formation, as the same chloride-capped complexes were isolated even in the presence of large excesses of bromide and iodide ions. As revealed by X-ray diffraction, all complexes are capped with a chloride ion via three N-H···Cl hydrogen bonds that stabilize their pseudomacrobicyclic frameworks. The MN6 coordination polyhedra possess a distorted trigonal prismatic geometry, with the distortion angles φ between their nonequivalent N3 bases of approximately 0°. Temperature dependences of the effective magnetic moment for the paramagnetic complexes showed the encapsulated metal(II) ions to be in a high-spin state in the temperature range of 2-300 K. In the case of the iron(II) pseudoclathrochelate, density functional theory (DFT) and time-dependent DFT calculations were used to assess its spin state as well as the (57)Fe Mössbauer and UV-vis-NIR parameters. Cyclic voltammetry studies performed for these pseudomacrobicyclic complexes showed them to undergo irreversible or quasi-reversible metal-localized oxidations and reductions. As no changes are observed in the presence of a substantial excess of bromide ion, no anion-exchange reaction occurs, and thus the pseudoclathrochelates have a high affinity toward chloride anions in solution.

  4. COMPARATIVE STUDY ON METAL IONS ADSORPTION ON A LOW COST CARBONACEOUS ADSORBENT KINETIC EQUILIBRIUM AND MECHANISTIC STUDIES

    Directory of Open Access Journals (Sweden)

    S. Arivoli, M. Hema, C. Barathiraja

    2008-01-01

    Full Text Available A carbonaceous adsorbent prepared from an indigenous waste and treated by acid was tested for its efficiency in removing metal ions of Fe(II, Co(II and Ni(II. The process parameters studied included agitation time, initial metal ion concentration, carbon dosage, pH, other ions and temperature. The kinetics of adsorption followed first order reaction equation and the rate was mainly controlled by intraparticle diffusion. Freundlich and Langmuir isotherm models were applied to the equilibrium data. The adsorption capacity obtained from the Langmuir isotherm plots was found around 28mg/g for all selected metal ions at an initial pH of 6. The temperature variation study showed that the metal ions adsorption is endothermic and spontaneous with increased randomness at the solid solution interface. Significant effect on adsorption was observed on varying pH of the metal ion solutions. The type I and II isotherms obtained, positive H0 values, pH dependent results and desorption of metal ions in mineral acid suggests that the adsorption of metal ions on this type of adsorbent involves both chemisorption and physical adsorption mechanisms.

  5. Irradiation of sorbents by ions of polymorphic metals for modeling 90strontium sedimentation.

    Science.gov (United States)

    Kurbatova, Elena I; Ksenofontov, Alexandre I; Dmitriyev, Alexey M; Regens, James L

    2007-06-01

    Advances in radioecology can support improvements in environmental remediation technologies, especially by illuminating interaction processes between polymorphic metal radionuclides and various materials and their ions in aqueous solutions. This study modeled interaction processes of 90Sr with transitive metals to delineate the behavior of polymorphic metal radionuclides. Experimental and modeling results confirmed Sr sedimentation was sensitive to the physical impact of radionuclides on various sorbents and possible chemical reactions occurring between the radionuclides and sorbents. Models were developed to simulate 90Sr sedimentation process, and the potential physical and chemical reactions accompanying the process. Models were verified, inorganic salts were used as sorbents to absorb metal cations, activity levels were recorded before and after mixing the inorganic salts while the efficiency of sedimentation using the heavy metals composites was quantified. This research demonstrates that the process of the sedimentation is complex and occurs in several stages. Micro-structural analysis shows that zones of interaction between the sorbent and source metal are formed during the irradiation of the target's metal surface. Electrical-microscopic analysis indicates that the composition of the formed zones of interaction of Ti (Sr) with target metals has various structures. Roentgenophase analysis indicates that the interaction of the ions of a precipitable source and a target occurs according to constitution diagrams of equilibrium systems. The results indicate that application of inorganic salts composites based on modeling increases the efficiency of the deactivation of aqueous solutions when compared to standard aluminum sulfate composite. Experimental and modeling results confirm 90Sr sedimentation is sensitive to the physical impact of radionuclides on various sorbents and possible chemical reactions occurring between the radionuclides and sorbents. The models

  6. Molar absorption coefficients and stability constants of Zincon metal complexes for determination of metal ions and bioinorganic applications.

    Science.gov (United States)

    Kocyła, Anna; Pomorski, Adam; Krężel, Artur

    2017-11-01

    Zincon (ZI) is one of the most common chromophoric chelating probes for the determination of Zn 2+ and Cu 2+ ions. It is also known to bind other metal ions. However, literature data on its binding properties and molar absorption coefficients are rather poor, varying among publications or determined only in certain conditions. There are no systematic studies on Zn 2+ and Cu 2+ affinities towards ZI performed under various conditions. However, this widely commercially available and inexpensive agent is frequently the first choice probe for the measurement of metal binding and release as well as determination of affinity constants of other ligands/macromolecules of interest. Here, we establish the spectral properties and the stability of ZI and its complexes with Zn 2+ , Cu 2+ , Cd 2+ , Hg 2+ , Co 2+ , Ni 2+ and Pb 2+ at multiple pH values from 6 to 9.9. The obtained results show that in water solution the MZI complex is predominant, but in the case of Co 2+ and Ni 2+ , M(ZI) 2 complexes are also formed. The molar absorption coefficient at 618 nm for ZnZI and 599nm for CuZI complexes at pH7.4 in buffered (I=0.1M) water solutions are 24,200 and 26,100M -1 cm -1 , respectively. Dissociation constants of those complexes are 2.09×10 -6 and 4.68×10 -17 M. We also characterized the metal-assisted Zincon decomposition. Our results provide new and reassessed optical and stability data that are applicable to a wide range of chemical and bioinorganic applications including metal ion detection, and quantification and affinity studies of ligands of interest. Accurate values of molar absorption coefficients of Zincon complex with Zn 2+ , Cd 2+ , Hg 2+ , Co 2+ , Ni 2+ , Cu 2+ , and Pb 2+ for rapid metal ion quantification are provided. Zincon stability constants with Zn 2+ and Cu 2+ in a wide pH range were determined. Copyright © 2017 Elsevier Inc. All rights reserved.

  7. High intensity metallic ion beam from an ecr ion source using the Mivoc method

    Energy Technology Data Exchange (ETDEWEB)

    Barue, C.; Canet, C.; Dupuis, M.; Flambard, J.L.; Leherissier, P.; Lemagnen, F. [Grand Accelerateur National d' Ions Lourds (GANIL), 14 - Caen (France); Jaffres, P.A. [Institut des Sciences de la Matiere et du Rayonnement, SIMRa, 14 - Cean (France)

    2000-07-01

    The MIVOC method has been successfully used at GANIL to produce a high intensity nickel beam with the ECR4 ion source: 20 {mu}A {sup 58}Ni{sup 11+} at 24 kV extraction voltage. This beam has been maintained for 8 days and accelerated up to 74.5 MeV/u by our cyclotrons with a mean intensity of 0.13 p{mu}A on target. This high intensity, required for experiment, led to the discovery of the doubly magic {sup 48}Ni isotope. Experimental setup, handling and off-line preparation using a residual gas analyzer are described in this report. The ion source behavior, performances and limitations are presented in the case of nickel and iron. The ionization efficiencies have been measured and compared to the oven method usually used at GANIL. (author)

  8. Spectroscopic and metal-binding properties of DF3: an artificial protein able to accommodate different metal ions

    Science.gov (United States)

    Torres Martin de Rosales, Rafael; Faiella, Marina; Farquhar, Erik; Que, Lawrence; Andreozzi, Concetta; Pavone, Vincenzo; Maglio, Ornella; Nastri, Flavia

    2010-01-01

    The design, synthesis, and metal-binding properties of DF3, a new de novo designed di-iron protein model are described (“DF” represents due ferri, Italian for “two iron,” “di-iron”). DF3 is the latest member of the DF family of synthetic proteins. They consist of helix–loop–helix hairpins, designed to dimerize and form an antiparallel four-helix bundle that encompasses a metal-binding site similar to those of non-heme carboxylate-bridged di-iron proteins. Unlike previous DF proteins, DF3 is highly soluble in water (up to 3 mM) and forms stable complexes with several metal ions (Zn, Co, and Mn), with the desired secondary structure and the expected stoichiometry of two ions per protein. UV–vis studies of Co(II) and Fe(III) complexes confirm a metal-binding environment similar to previous di-Co(II)- and di-Fe(III)-DF proteins, including the presence of a µ-oxo-di-Fe(III) unit. Interestingly, UV–vis, EPR, and resonance Raman studies suggest the interaction of a tyro-sine adjacent to the di-Fe(III) center. The design of DF3 was aimed at increasing the accessibility of small molecules to the active site of the four-helix bundle. Indeed, binding of azide to the di-Fe(III) site demonstrates a more accessible metal site compared with previous DFs. In fact, fitting of the binding curve to the Hill equation allows us to quantify a 150% accessibility enhancement, with respect to DF2. All these results represent a significant step towards the development of a functional synthetic DF metalloprotein. PMID:20225070

  9. General Synthesis of Transition-Metal Oxide Hollow Nanospheres/Nitrogen-Doped Graphene Hybrids by Metal-Ammine Complex Chemistry for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Chen, Jiayuan; Wu, Xiaofeng; Gong, Yan; Wang, Pengfei; Li, Wenhui; Mo, Shengpeng; Peng, Shengpan; Tan, Qiangqiang; Chen, Yunfa

    2018-02-09

    We present a general and facile synthesis strategy, on the basis of metal-ammine complex chemistry, for synthesizing hollow transition-metal oxides (Co 3 O 4 , NiO, CuO-Cu 2 O, and ZnO)/nitrogen-doped graphene hybrids, potentially applied in high-performance lithium-ion batteries. The oxygen-containing functional groups of graphene oxide play a prerequisite role in the formation of hollow transition-metal oxides on graphene nanosheets, and a significant hollowing process occurs only when forming metal (Co 2+ , Ni 2+ , Cu 2+ , or Zn 2+ )-ammine complex ions. Moreover, the hollowing process is well correlated with the complexing capacity between metal ions and NH 3 molecules. The significant hollowing process occurs for strong metal-ammine complex ions including Co 2+ , Ni 2+ , Cu 2+ , and Zn 2+ ions, and no hollow structures formed for weak and/or noncomplex Mn 2+ and Fe 3+ ions. Simultaneously, this novel strategy can also achieve the direct doping of nitrogen atoms into the graphene framework. The electrochemical performance of two typical hollow Co 3 O 4 or NiO/nitrogen-doped graphene hybrids was evaluated by their use as anodic materials. It was demonstrated that these unique nanostructured hybrids, in contrast with the bare counterparts, solid transition-metal oxides/nitrogen-doped graphene hybrids, perform with significantly improved specific capacity, superior rate capability, and excellent capacity retention. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Intercalation of Coordinatively Unsaturated Fe(III) Ion within Interpenetrated Metal-Organic Framework MOF-5.

    Science.gov (United States)

    Holmberg, Rebecca J; Burns, Thomas; Greer, Samuel M; Kobera, Libor; Stoian, Sebastian A; Korobkov, Ilia; Hill, Stephen; Bryce, David L; Woo, Tom K; Murugesu, Muralee

    2016-06-01

    Coordinatively unsaturated Fe(III) metal sites were successfully incorporated into the iconic MOF-5 framework. This new structure, Fe(III) -iMOF-5, is the first example of an interpenetrated MOF linked through intercalated metal ions. Structural characterization was performed with single-crystal and powder XRD, followed by extensive analysis by spectroscopic methods and solid-state NMR, which reveals the paramagnetic ion through its interaction with the framework. EPR and Mössbauer spectroscopy confirmed that the intercalated ions were indeed Fe(III) , whereas DFT calculations were employed to ascertain the unique pentacoordinate architecture around the Fe(III) ion. Interestingly, this is also the first crystallographic evidence of pentacoordinate Zn(II) within the MOF-5 SBU. This new MOF structure displays the potential for metal-site addition as a framework connector, thus creating further opportunity for the innovative development of new MOF materials. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. In vivo effects of metal ions on conformation and mechanical performance of silkworm silks.

    Science.gov (United States)

    Wang, Xin; Li, Yi; Liu, Qingsong; Chen, Quanmei; Xia, Qingyou; Zhao, Ping

    2017-03-01

    The mechanism of silk fiber formation is of particular interest. Although in vitro evidence has shown that metal ions affect conformational transitions of silks, the in vivo effects of metal ions on silk conformations and mechanical performance are still unclear. This study explored the effects of metal ions on silk conformations and mechanical properties of silk fibers by adding K+ and Cu2+ into the silk fibroin solutions or injecting them into the silkworms. Aimed by CD analysis, FTIR analysis, and mechanical testing, the conformational and mechanical changes of the silks were estimated. By using BION Web Server, the interactions of K+ and N-terminal of silk fibroin were also simulated. We presented that K+ and Cu2+ induced the conformational transitions of silk fibroin by forming β-sheet structures. Moreover, the mechanical parameters of silk fibers, such as strength, toughness and Young's modulus, were also improved after K+ or Cu2+ injection. Using BION Web Server, we found that potassium ions may have strong electrostatic interactions with the negatively charged residues. We suggest that K+ and Cu2+ play crucial roles in the conformation and mechanical performances of silks and they are involved in the silk fiber formation in vivo. Our results are helpful for clarifying the mechanism of silk fiber formation, and provide insights for modifying the mechanical properties of silk fibers. Copyright © 2016 Elsevier B.V. All rights reserved.

  12. 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.

  13. High depth resolution SIMS analysis using metal cluster complex ion bombardment

    Energy Technology Data Exchange (ETDEWEB)

    Tomita, M; Kinno, T; Koike, M; Tanaka, H; Takeno, S [Corporate Research and Development Center, Toshiba Corporation, 8 Shinsugita-cho, Isogo-ku, Yokohama 235-8522 (Japan); Fujiwara, Y; Kondou, K; Teranishi, Y; Nonaka, H; Fujimoto, T; Kurokawa, A; Ichimura, S [National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 2, 1-1-1 Umezono, Tsukuba-shi, Ibaraki-ken 305-8568 (Japan)], E-mail: mitsuhiro.tomita@toshiba.co.jp

    2008-03-15

    SIMS depth profiles were measured using metal cluster complex ions of Ir{sub 4}(CO){sub 7}{sup +} as a primary ion beam in order to obtain high depth resolution. Depth resolution was evaluated as a function of primary ion species, energy and incident angle using a multiple boron delta-doped silicon sample. The depth resolution obtained using cluster ion bombardment was considerably better than that obtained by oxygen ion bombardment under the same bombardment condition due to reduction of atomic mixing in the depth. The best depth resolution was 0.9 nm under the bombardment condition of 5 keV, 45 deg. with oxygen flooding, which approaches the value measured with state of the art SIMS analyses. However, depth resolution was not improved by decreasing the cluster ion energy (less than 5 keV), even though the roughness of the sputtered surface was suppressed. The limit of depth resolution improvement may be caused by a carbon cover-layer that prevents the formation of surface oxide that buffers atomic mixing. To overcome this issue, it will be necessary to eliminate carbon from the cluster ion.

  14. Selectivity and permeation in calcium release channel of cardiac muscle: alkali metal ions.

    Science.gov (United States)

    Chen, D P; Xu, L; Tripathy, A; Meissner, G; Eisenberg, B

    1999-03-01

    Current was measured from single open channels of the calcium release channel (CRC) of cardiac sarcoplasmic reticulum (over the range +/-180 mV) in pure and mixed solutions (e.g., biionic conditions) of the alkali metal ions Li+, K+, Na+, Rb+, Cs+, ranging in concentration from 25 mM to 2 M. The current-voltage (I-V) relations were analyzed by an extension of the Poisson-Nernst-Planck (PNP) formulation of electrodiffusion, which includes local chemical interaction described by an offset in chemical potential, which likely reflects the difference in dehydration/solvation/rehydration energies in the entry/exit steps of permeation. The theory fits all of the data with few adjustable parameters: the diffusion coefficient of each ion species, the average effective charge distribution on the wall of the pore, and an offset in chemical potential for lithium and sodium ions. In particular, the theory explains the discrepancy between "selectivities" defined by conductance sequence and "selectivities" determined by the permeability ratios (i.e., reversal potentials) in biionic conditions. The extended PNP formulation seems to offer a successful combined treatment of selectivity and permeation. Conductance selectivity in this channel arises mostly from friction: different species of ions have different diffusion coefficients in the channel. Permeability selectivity of an ion is determined by its electrochemical potential gradient and local chemical interaction with the channel. Neither selectivity (in CRC) seems to involve different electrostatic interaction of different ions with the channel protein, even though the ions have widely varying diameters.

  15. Determination of metal ions released by stainless steel arch bar into bio-fluids

    Directory of Open Access Journals (Sweden)

    Lori A. Joseph

    2009-04-01

    Full Text Available 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 six-week immersion time at 37 oC, by atomic absorption spectrophotometry. The corrosion levels of the wires due to effects of media and incubation times in the bio-fluids were compared by Duncan’s two-way ANOVA (P less than 0.05. Pearson’s correlation was used in establishing relationship in the amounts of metal ions released by new and reused arch bars. The study indicated that the reused wires released more ions than new ones at all time points. The variation of pH and chloride ions of the bio-fluids had a significant effect on the amount of Ni, Mn and Cr ions released. Ageing prior use of arch bars significantly increased Ni ions released into the bio-fluids.

  16. Semi-Interpenetrating Polymer Networks with Predefined Architecture for Metal Ion Fluorescence Monitoring

    Directory of Open Access Journals (Sweden)

    Kyriakos Christodoulou

    2016-11-01

    Full Text Available The development of new synthetic approaches for the preparation of efficient 3D luminescent chemosensors for transition metal ions receives considerable attention nowadays, owing to the key role of the latter as elements in biological systems and their harmful environmental effects when present in aquatic media. In this work, we describe an easy and versatile synthetic methodology that leads to the generation of nonconjugated 3D luminescent semi-interpenetrating amphiphilic networks (semi-IPN with structure-defined characteristics. More precisely, the synthesis involves the encapsulation of well-defined poly(9-anthrylmethyl methacrylate (pAnMMA (hydrophobic, luminescent linear polymer chains within a covalent poly(2-(dimethylaminoethyl methacrylate (pDMAEMA hydrophilic polymer network, derived via the 1,2-bis-(2-iodoethoxyethane (BIEE-induced crosslinking process of well-defined pDMAEMA linear chains. Characterization of their fluorescence properties demonstrated that these materials act as strong blue emitters when exposed to UV irradiation. This, combined with the presence of the metal-binding tertiary amino functionalities of the pDMAEMA segments, allowed for their applicability as sorbents and fluorescence chemosensors for transition metal ions (Fe3+, Cu2+ in solution via a chelation-enhanced fluorescence-quenching effect promoted within the semi-IPN network architecture. Ethylenediaminetetraacetic acid (EDTA-induced metal ion desorption and thus material recyclability has been also demonstrated.

  17. CONSIDERATIONS REGARDING THE INFLUENCE OF METALIC IONS OF THE STABILITY OF CARBONATES FROM SOILS

    Directory of Open Access Journals (Sweden)

    D. Bulgariu

    2005-10-01

    Full Text Available The distribution of minor elements in heterogeneous mineral / aqueous solutions systems represent one of important problem, with many applications in environmental geochemistry field. Ours studies was focus on the metal ions distribution in carbonate (CaCO3 / solution systems, from applicability point of view to the estimation of formation conditions and of carbonates stability from soils. On the base of our results obtained by sequential solid / liquid extraction for 17 soil samples and theoretical modeling of CaCO3 / solution systems, and the results from literature we try to develop the McIntire prognosis models and the free Gibbs enthalpy linear correlation model, by the inclusion in calculus relations of distribution coefficients a higher number of factors which effective influenced the thermodynamics and kinetics of interphase distribution processes of metal ions. The established correlations has been used to the estimation of time evolution of carbonate / solution equilibrium under the influence of some metal ions (Cd, Zn, Cu, Pb, Bi, which appear usual as pollutants in soils. The prognosis realized on the base of the established correlations are in agreement with the theoretical modelling results and studies of case for different types of polluted soils with heavy metals.

  18. Sensitivity to Heavy-Metal Ions of Unfolded Fullerene Quantum Dots

    Directory of Open Access Journals (Sweden)

    Erica Ciotta

    2017-11-01

    Full Text Available A novel type of graphene-like quantum dots, synthesized by oxidation and cage-opening of C60 buckminsterfullerene, has been studied as a fluorescent and absorptive probe for heavy-metal ions. The lattice structure of such unfolded fullerene quantum dots (UFQDs is distinct from that of graphene since it includes both carbon hexagons and pentagons. The basic optical properties, however, are similar to those of regular graphene oxide quantum dots. On the other hand, UFQDs behave quite differently in the presence of heavy-metal ions, in that multiple sensitivity to Cu2+, Pb2+ and As(III was observed through comparable quenching of the fluorescent emission and different variations of the transmittance spectrum. By dynamic light scattering measurements and transmission electron microscope (TEM images we confirmed, for the first time in metal sensing, that this response is due to multiple complexation and subsequent aggregation of UFQDs. Nonetheless, the explanation of the distinct behaviour of transmittance in the presence of As(III and the formation of precipitate with Pb2+ require further studies. These differences, however, also make it possible to discriminate between the three metal ions in view of the implementation of a selective multiple sensor.

  19. Engineering Metal Ion Coordination to Regulate Amyloid Fibril Assembly And Toxicity

    Energy Technology Data Exchange (ETDEWEB)

    Dong, J.; Canfield, J.M.; Mehta, A.K.; Shokes, J.E.; Tian, B.; Childers, W.S.; Simmons, J.A.; Mao, Z.; Scott, R.A.; Warncke, K.; Lynn, D.G.

    2009-06-02

    Protein and peptide assembly into amyloid has been implicated in functions that range from beneficial epigenetic controls to pathological etiologies. However, the exact structures of the assemblies that regulate biological activity remain poorly defined. We have previously used Zn{sup 2+} to modulate the assembly kinetics and morphology of congeners of the amyloid {beta} peptide (A{beta}) associated with Alzheimer's disease. We now reveal a correlation among A{beta}-Cu{sup 2+} coordination, peptide self-assembly, and neuronal viability. By using the central segment of A{beta}, HHQKLVFFA or A{beta}(13-21), which contains residues H13 and H14 implicated in A{beta}-metal ion binding, we show that Cu{sup 2+} forms complexes with A{beta}(13-21) and its K16A mutant and that the complexes, which do not self-assemble into fibrils, have structures similar to those found for the human prion protein, PrP. N-terminal acetylation and H14A substitution, Ac-A{beta}(13-21)H14A, alters metal coordination, allowing Cu{sup 2+} to accelerate assembly into neurotoxic fibrils. These results establish that the N-terminal region of A{beta} can access different metal-ion-coordination environments and that different complexes can lead to profound changes in A{beta} self-assembly kinetics, morphology, and toxicity. Related metal-ion coordination may be critical to the etiology of other neurodegenerative diseases.

  20. Non-Native Metal Ion Reveals the Role of Electrostatics in Synaptotagmin 1-Membrane Interactions.

    Science.gov (United States)

    Katti, Sachin; Nyenhuis, Sarah B; Her, Bin; Srivastava, Atul K; Taylor, Alexander B; Hart, P John; Cafiso, David S; Igumenova, Tatyana I

    2017-06-27

    C2 domains are independently folded modules that often target their host proteins to anionic membranes in a Ca2+-dependent manner. In these cases, membrane association is triggered by Ca2+ binding to the negatively charged loop region of the C2 domain. Here, we used a non-native metal ion, Cd2+, in lieu of Ca2+ to gain insight into the contributions made by long-range Coulombic interactions and direct metal ion-lipid bridging to membrane binding. Using X-ray crystallography, NMR, Förster resonance energy transfer, and vesicle cosedimentation assays, we demonstrate that, although Cd2+ binds to the loop region of C2A/B domains of synaptotagmin 1 with high affinity, long-range Coulombic interactions are too weak to support membrane binding of individual domains. We attribute this behavior to two factors: the stoichiometry of Cd2+ binding to the loop regions of the C2A and C2B domains and the impaired ability of Cd2+ to directly coordinate the lipids. In contrast, electron paramagnetic resonance experiments revealed that Cd2+ does support membrane binding of the C2 domains in full-length synaptotagmin 1, where the high local lipid concentrations that result from membrane tethering can partially compensate for lack of a full complement of divalent metal ions and specific lipid coordination in Cd2+-complexed C2A/B domains. Our data suggest that long-range Coulombic interactions alone can drive the initial association of C2A/B with anionic membranes and that Ca2+ further augments membrane binding by the formation of metal ion-lipid coordination bonds and additional Ca2+ ion binding to the C2 domain loop regions.

  1. Distinct differences in metal ion specificity of RNA and DNA G-quadruplexes.

    Science.gov (United States)

    Guiset Miserachs, Helena; Donghi, Daniela; Börner, Richard; Johannsen, Silke; Sigel, Roland K O

    2016-12-01

    RNA G-quadruplexes, as their well-studied DNA analogs, require the presence of cations to fold and remain stable. This is the first comprehensive study on the interaction of RNA quadruplexes with metal ions. We investigated the formation and stability of two highly conserved and biologically relevant RNA quadruplex-forming sequences (24nt-TERRA and 18nt-NRAS) in the presence of several monovalent and divalent metal ions, namely Li + , Na + , K + , Rb + , Cs + , NH 4 + , Mg 2+ , Ca 2+ , Sr 2+ , and Ba 2+ . Circular dichroism was used to probe the influence of these metal ions on the folded fraction of the parallel G-quadruplexes, and UV thermal melting experiments allowed to assess the relative stability of the structures in each cationic condition. Our results show that the RNA quadruplexes are more stable than their DNA counterparts under the same buffer conditions. We have observed that the addition of mainly Na + , K + , Rb + , NH 4 + , as well as Sr 2+ and Ba 2+ in water, shifts the equilibrium to the folded quadruplex form, whereby the NRAS sequence responds stronger than TERRA. However, only K + and Sr 2+ lead to a significant increase in the stability of the folded structures, which is consistent with their coordination to the O6 atoms from the G-quartet guanosines. Compared to the respective DNA motives, dNRAS and htelo, the RNA sequences are not stabilized by Na + ions. Finally, the difference in response between NRAS and TERRA, as well as to the corresponding DNA sequences with respect to different metal ions, could potentially be exploited for selective targeting purposes.

  2. Metal ion dependence of DNA cleavage by SepMI and EhoI restriction endonucleases.

    Science.gov (United States)

    Belkebir, Abdelkarim; Azeddoug, Houssine

    2013-02-22

    Most of type II restriction endonucleases show an absolute requirement for divalent metal ions as cofactors for DNA cleavage. While Mg(2+) is the natural cofactor other metal ions can substitute it and mediate the catalysis, however Ca(2+) (alone) only supports DNA binding. To investigate the role of Mg(2+) in DNA cleavage by restriction endonucleases, we have studied the Mg(2+) and Mn(2+) concentration dependence of DNA cleavage by SepMI and EhoI. Digestion reactions were carried out at different Mg(2+) and Mn(2+) concentrations at constant ionic strength. These enzymes showed different behavior regarding the ions requirement, SepMI reached near maximal level of activity between 10 and 20mM while no activity was detected in the presence of Mn(2+) and in the presence of Ca(2+) cleavage activity was significantly decreased. However, EhoI was more highly active in the presence of Mn(2+) than in the presence of Mg(2+) and can be activated by Ca(2+). Our results propose the two-metal ion mechanism for EhoI and the one-metal ion mechanism for SepMI restriction endonuclease. The analysis of the kinetic parameters under steady state conditions showed that SepMI had a K(m) value for pTrcHisB DNA of 6.15 nM and a V(max) of 1.79×10(-2)nM min(-1), while EhoI had a K(m) for pUC19 plasmid of 8.66 nM and a V(max) of 2×10(-2)nM min(-1). Copyright © 2012 Elsevier GmbH. All rights reserved.

  3. Metal ion complexation by ionizable crown ethers. Final report, January 1, 1988--June 30, 1994

    Energy Technology Data Exchange (ETDEWEB)

    Bartsch, R.A.

    1994-12-31

    During the report period a variety of new lipophilic ionizable crown ethers with pendent proton-ionizable groups has been synthesized. The ligands possess one or more ionizable group (carboxylic acid, phosphonic acid monoethyl ester, para-nitrophenol, phosphonic acid) attached to crown ether, monoazacrown ether or diazacrown ether frameworks. These novel chelating agents have either pendent or inward-facing proton-ionizable groups. Such lipophilic proton-ionizable crown ethers are designed for use in multiphase metal ion separations (solvent extraction, liquid membrane transport). In addition a series of proton-ionizable crown ethers without lipophilic groups was prepared to study how structural variations within the ligand influence metal ion complexation in homogeneous media as assessed by NMR spectroscopy or titration calorimetry. A third class of new metal ion-complexing agents is a series of lipophilic acyclic polyether dicarboxylic acids. Competitive solvent extractions of alkali metal and alkaline earth cations and of the mixed species have been conducted to reveal the influence of ring size, nature and attachment site of the lipophilic group, sidearm length, and proton-ionizable group identity and location upon the selectivity and efficiency of metal ion complexation. In addition to such studies of structural variation within the lipophilic proton-ionizable crown ether, the effect of changing the organic solvent and variation of the stripping conditions have been assessed. The influence of structural variations within lipophilic acyclic polyether dicarboxylic acids upon competitive solvent extraction of alkaline earth cations has been probed. Also a new chromogenic, di-ionizable crown ether with extremely high selectivity for Hg{sup 2+} has been discovered.

  4. Recent advances in DNA-based electrochemical biosensors for heavy metal ion detection: A review.

    Science.gov (United States)

    Saidur, M R; Aziz, A R Abdul; Basirun, W J

    2017-04-15

    The presence of heavy metal in food chains due to the rapid industrialization poses a serious threat on the environment. Therefore, detection and monitoring of heavy metals contamination are gaining more attention nowadays. However, the current analytical methods (based on spectroscopy) for the detection of heavy metal contamination are often very expensive, tedious and can only be handled by trained personnel. DNA biosensors, which are based on electrochemical transduction, is a sensitive but inexpensive method of detection. The principles, sensitivity, selectivity and challenges of electrochemical biosensors are discussed in this review. This review also highlights the major advances of DNA-based electrochemical biosensors for the detection of heavy metal ions such as Hg 2+ , Ag + , Cu 2+ and Pb 2+ . Copyright © 2016 Elsevier B.V. All rights reserved.

  5. Production of Hydrated Metal Ions by Fast Ion or Atom Beam Sputtering. Collision-Induced Dissociation and Successive Hydration Energies of Gaseous Cu+ with 1-4 Water Molecules

    NARCIS (Netherlands)

    Magnera, Thomas F.; David, Donald E.; Stulik, Dusan; Orth, Robert G.; Jonkman, Harry T.; Michl, Josef

    1989-01-01

    Low-temperature sputtering of frozen aqueous solutions of metal salts, of hydrated crystalline transition-metal salts, of frosted metal surfaces, and of frosted metal salts with kiloelectronvolt energy rare gas atoms or ions produces copious amounts of cluster ions, among which M+(H2O)n and/or

  6. Theoretical and experimental studies on isotachophoresis in multi-moving chelation boundary system formed with metal ions and EDTA.

    Science.gov (United States)

    Zhang, Wei; Guo, Chen-Gang; Fan, Liu-Yin; Cao, Cheng-Xi

    2013-09-07

    In this paper, a general mode and theory of moving chelation boundary based isotachophoresis (MCB-based ITP), together with the concept of decisive metal ion (DMI) having the maximum complexation constant (lg Kmax) with the chelator, were developed from a multi-MCB (mMCB) system. The theoretical deductions were: (i) the reaction boundary velocities in the mMCB system at steady state were equal to each other, resulting in a novel MCB-based ITP separation of metal ions; (ii) the boundary directions and velocities in the system were controlled by the fluxes of chelator and DMI, rather than other metal ions; and (iii) a controllable stacking of metal ions could be simultaneously achieved in the developed system. To demonstrate the deductions, a series of experiments were conducted by using model chelator of EDTA and metal ions of Cu(II) and Co(II) due to characteristic colors of blue [Cu-EDTA](2-) and pink [Co-EDTA](2-) complexes. The experiments demonstrated the correctness of theoretical deductions, indicating the validity of the developed model and theory of ITP. These findings provide guidance for the development of MRB-based ITP separation and stacking of metal ions in biological sample matrix and heavy metal ions in environmental samples.

  7. Clinical Results and Serum Metal Ion Concentrations following Ceramic-on-Metal Total Hip Arthroplasty at a Mean Follow-Up of 60 Months

    Directory of Open Access Journals (Sweden)

    W. Maurer-Ertl

    2017-01-01

    Full Text Available Background. Increased metal ion levels following total hip arthroplasty (THA with metal-on-metal bearings are a highly debated topic. Local soft tissue reactions with chronic pain and systemic side effects such as neuropathy are described. The aim of the current study was to determine the serum metal ion concentrations of Cobalt (Co and Chrome (Cr after THA with a ceramic-on-metal (CoM bearing. Patients and Methods. Between 2008 and 2010, 20 patients underwent THA using a CoM bearing. Clinical function was evaluated by standardized scores systems (Harris Hip Score and WOMAC Score and radiological examination included X-rays. Patient’s blood samples were obtained for metal ion analysis and correlation analysis was done between these results and implant position. Results. Overall, 13 patients with 14 CoM devices were available for the current series. The mean age at time of surgery was 61 years (range, 41 to 85. The postoperative follow-up ranged from 49 to 68 months (mean, 58. Metal ion determination showed mean concentrations of 3,1 µg/L (range, 0,3–15,2 µg/L for Co and 1,6 µg/L (range, 0,1–5,5 µg/L for Cr, respectively. A correlation between cup anteversion and Co and Cr concentrations was shown. Conclusion. The current series showed increments for Co and Cr following CoM THA. However, these levels are lower compared to metal ion concentrations in patients with metal-on-metal bearings and the international accepted threshold for revision of MoM devices. We recommend routine follow-up including at least one obligatory evaluation of serum metal ion concentrations and an MRI once to exclude local soft tissue reactions.

  8. Rational composition control of mixed-lanthanide metal-organic frameworks by an interfacial reaction with metal ion-doped polymer substrates

    Science.gov (United States)

    Tsuruoka, Takaaki; Miyanaga, Ayumi; Ohhashi, Takashi; Hata, Manami; Takashima, Yohei; Akamatsu, Kensuke

    2017-09-01

    A simple composition control route to mixed-lanthanide metal-organic frameworks (MOFs) was developed based on an interfacial reaction with mixed-lanthanide metal ion-doped polymer substrates. By controlling the composition of lanthanide ion (Eu3+ and Tb3+) dopants in polymer substrates to be used as metal ion precursors and scaffolding for the formation of MOFs, [EuxTb2-x(bdc)3(H2O)4]n crystals with a tunable metal composition could be routinely prepared on polymer substrates. Inductively coupled plasma (ICP) measurements revealed that the composition of the obtained frameworks was almost the same as that of the initial polymer substrates. In addition, the resulting [EuxTb2-x(bdc)3(H2O)4]n crystals showed strong phosphorescence because of Eu3+ transitions, indicating that the energy transfer from Tb3+ to Eu3+ ions in the frameworks could be achieved with high efficiency.

  9. 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.

  10. Luminescent microporous metal-organic framework with functional lewis basic sites on the pore surface: specific sensing and removal of metal ions.

    Science.gov (United States)

    Jayaramulu, Kolleboyina; Narayanan, Raghu Pradeep; George, Subi J; Maji, Tapas Kumar

    2012-10-01

    A three-dimensional luminescent metal-organic framework, {Mg(DHT)(DMF)(2)}(n) (1), based on an excited-state intramolecular proton-transfer (ESIPT) responsive linker, 2,5-dihydroxyterephthalic acid (H(2)DHT), has been synthesized, and its desolvated microporous framework with pendent -OH groups on the pore surface was exploited for the binding and specific sensing of metal ions via Lewis acid-base interactions. The luminescence intensity significantly quenches with Cu(II) among various s- and d-block metal ions, and highly selective sensing of Cu(II) ions has been realized in both solid and solution states (up to nanomolar concentration). The immobilized Cu(II) metal ions can be selectively removed by chelating agents like ethylenediaminetetraacetic acid without any structural disintegration of the framework, as revealed by the luminescence and gas-adsorption studies.

  11. APPLICATION OF PRINCIPAL COMPONENTS ANALYSIS IN THE STUDY OF ADSORPTIVE VOLTAMMETRY OF METALICS IONS

    Directory of Open Access Journals (Sweden)

    Leandra de Oliveira Cruz da Silva

    2010-01-01

    Full Text Available The adsorptive stripping voltammetry with differential pulse cathodic through the use of a mixture of complexing agents dimethylglyoxime and oxine was used for an exploratory study simultaneously of ions cadmium, cobalt, copper, nickel, lead and zinc. Were obtained voltammograms of the 64 individual solutions used in planning and current data were submitted to principal component analysis (PCA, allowing to characterize the trends of the solutions of metal ions studied. The system can be described in eight principal components that explained 98.32% of variance. Since the first three principal components accumulated approximately 85.46% of the total variance.

  12. Transition metal swift heavy ion implantation on 4H-SiC

    Energy Technology Data Exchange (ETDEWEB)

    Ali, A. Ashraf; Kumar, J. [Crystal Growth Centre, Anna University, Chennai 600 025 (India); Ramakrishnan, V. [Indian Institute of Science Education and Research, Thiruvanthapuram (India); Asokan, K. [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110 067 (India)

    2016-03-01

    This work reports on the realization of Quantum Ring (QR) and Quantum Dot (QD) like structures on 4H-SiC through SHI implantation and on their Raman studies. 4H-SiC is SHI implanted with Transition Metal (TM) Ni ion at different fluences. It is observed that a vibrational mode emerges as the result of Ni ion implantation. The E{sub 2} (TO) and the A{sub 1} (LO) are suppressed as the fluence increases. In this paper Raman and AFM studies have been performed at room temperature and the queer anomalies are addressed so new devices can be fabricated.

  13. The influence of metal artefacts on the range of ion beams

    Energy Technology Data Exchange (ETDEWEB)

    Jaekel, Oliver; Reiss, Petra [German Cancer Research Center - Deutsches Krebsforschungszentrum, Division for Medical Physics in Radiotherapy (E040), Im Neuenheimer Feld 280, 69120 Heidelberg (Germany)

    2007-02-07

    The influence of artefacts due to metal implants on the range of ion beams is investigated, using a geometrically well-defined head and pelvic phantom together with inserts from steel, titanium and tungsten. The ranges along various beam paths including artefacts were calculated from the TPS and compared to known calculations for phantoms without any insert. In the head phantom, beams intersecting the streak artefacts lead to errors in the range of around or below 1%, which is mainly due to a cancellation of various effects. Beams through the metal or close to it show an underestimation of 3.5% of the range for tungsten. For the pelvic phantom, a large underestimation of the range is observed for a lateral path through the metal insert. In the case of tungsten and steel, range errors of -5% and -18% are observed, respectively. Such beam paths are typically used for pelvic tumours in radiotherapy with ion beams. For beams in the anterior-posterior direction through the inserts, an overestimation of ion ranges of up to 3% for titanium and 8% for steel is expected, respectively. Beam paths outside the metal insert show a large cancellation for the lateral beams (leading to errors of around 1% only) and somewhat higher errors for anterior-posterior beams (around 3% for titanium and 6% for steel). The analysis of CT data of patients with dental implants of gold as compared to patients with healthy teeth also showed a significant effect of the artefacts on the distribution of HU in the data, namely a redistribution of HU to higher and lower values as compared to patients with healthy teeth. The corresponding mean range variation was a 2.5% reduction in the data with artefacts as compared to the data without artefacts. It is concluded that beam paths through metal implants should generally be avoided in proton and ion therapy. In this case, the underestimation of ion range due to artefacts alone may amount to 3% for dental fillings and up to 5% and 18% for hip prosthesis

  14. 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

  15. pH-Dependent metal ion toxicity influences the antibacterial activity of two natural mineral mixtures.

    Directory of Open Access Journals (Sweden)

    Tanya M Cunningham

    2010-03-01

    Full Text Available Recent studies have demonstrated that several mineral products sold for medicinal purposes demonstrate antimicrobial activity, but little is known about the physicochemical properties involved in antibacterial activity.Using in vitro mineral suspension testing, we have identified two natural mineral mixtures, arbitrarily designated BY07 and CB07, with antibacterial activity against a broad-spectrum of bacterial pathogens. Mineral-derived aqueous leachates also exhibited antibacterial activity, revealing that chemical, not physical, mineral characteristics were responsible for the observed activity. The chemical properties essential for bactericidal activity against Escherichia coli were probed by testing antibacterial activity in the presence of metal chelators, the hydroxyl radical scavenger, thiourea, and varying pH levels. Chelation of the BY07 minerals with EDTA or desferrioxamine eliminated or reduced BY07 toxicity, respectively, suggesting a role of an acid-soluble metal species, particularly Fe(3+ or other sequestered metal cations, in mineral toxicity. This conclusion was supported by NMR relaxation data, which indicated that BY07 and CB07 leachates contained higher concentrations of chemically accessible metal ions than leachates from non-bactericidal mineral samples.We conclude that the acidic environment of the hydrated minerals significantly contributes to antibacterial activity by increasing the availability and toxicity of metal ions. These findings provide impetus for further investigation of the physiological effects of mineral products and their applications in complementary antibacterial therapies.

  16. Reactions of metallic Li or LiC6 with organic solvents for lithium ion battery

    Science.gov (United States)

    Nakajima, Tsuyoshi; Hirobayashi, Yuki; Takayanagi, Yuki; Ohzawa, Yoshimi

    2013-12-01

    DSC (Differential Scanning Calorimetry) study has been made on the reactions of metallic Li or LiC6 with organic solvents for lithium ion battery. Ethylene carbonate (EC) more easily reacts with metallic Li and LiC6 than propylene carbonate (PC). This may be because formation of lithium alkyl carbonate is more difficult for PC than EC. On the other hand, diethyl carbonate (DEC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) react with Li in the same manner. Reactions of Li and LiC6 with organic solvents have been discussed based on the results of quantum calculation.

  17. Where does the toxicity of metal oxide nanoparticles come from: The nanoparticles, the ions, or a combination of both?

    Science.gov (United States)

    Wang, Dali; Lin, Zhifen; Wang, Ting; Yao, Zhifeng; Qin, Mengnan; Zheng, Shourong; Lu, Wei

    2016-05-05

    The toxicity of metal oxide nanoparticles (NPs) has aroused great concern over the past few years. However, there still remains the question whether the toxicity of the metal oxide NPs originates from the released ions or the NPs themselves. In this study, the metal ion release of CuO, Fe2O3, ZnO, Co3O4, Cr2O3, and NiO NPs in aqueous media was investigated, and their contributions to the metal oxide NPs' inhibition on the bioluminescence of Photobacterium phosphoreum were studied. It was found that the ions release of the metal oxide NPs in aqueous media was complex, depending on both the dissolution and adsorption processes of the metal oxide NPs. The relationships between the metal oxide NPs' antibacterial effects and their released metal ions could be divided into three categories: (1) the ZnO NPs' antibacterial effect was due solely to the released Zn(2+); (2) the CuO NPs' antibacterial effect originated from both the released Cu(2+),and the CuO particles; and (3) the antibacterial effects of Fe2O3, Co3O4, Cr2O3, and NiO NPs were caused by the NPs themselves. Our findings suggest that the ions release and their contributions to the NPs' toxicity should be considered in the toxicity evaluations of the metal oxide NPs. Copyright © 2016 Elsevier B.V. All rights reserved.

  18. Role of Metal Ions on the Activity of Mycobacterium tuberculosis Pyrazinamidase

    Science.gov (United States)

    Sheen, Patricia; Ferrer, Patricia; Gilman, Robert H.; Christiansen, Gina; Moreno-Román, Paola; Gutiérrez, Andrés H.; Sotelo, Jun; Evangelista, Wilfredo; Fuentes, Patricia; Rueda, Daniel; Flores, Myra; Olivera, Paula; Solis, José; Pesaresi, Alessandro; Lamba, Doriano; Zimic, Mirko

    2012-01-01

    Pyrazinamidase of Mycobacterium tuberculosis catalyzes the conversion of pyrazinamide to the active molecule pyrazinoic acid. Reduction of pyrazinamidase activity results in a level of pyrazinamide resistance. Previous studies have suggested that pyrazinamidase has a metal-binding site and that a divalent metal cofactor is required for activity. To determine the effect of divalent metals on the pyrazinamidase, the recombinant wild-type pyrazinamidase corresponding to the H37Rv pyrazinamide-susceptible reference strain was expressed in Escherichia coli with and without a carboxy terminal. His-tagged pyrazinamidase was inactivated by metal depletion and reactivated by titration with divalent metals. Although Co2+, Mn2+, and Zn2+ restored pyrazinamidase activity, only Co2+ enhanced the enzymatic activity to levels higher than the wild-type pyrazinamidase. Cu2+, Fe2+, Fe3+, and Mg2+ did not restore the activity under the conditions tested. Various recombinant mutated pyrazinamidases with appropriate folding but different enzymatic activities showed a differential pattern of recovered activity. X-ray fluorescence and atomic absorbance spectroscopy showed that recombinant wild-type pyrazinamidase expressed in E. coli most likely contained Zn. In conclusion, this study suggests that M. tuberculosis pyrazinamidase is a metalloenzyme that is able to coordinate several ions, but in vivo, it is more likely to coordinate Zn2+. However, in vitro, the metal-depleted enzyme could be reactivated by several divalent metals with higher efficiency than Zn. PMID:22764307

  19. Interaction between coordinated metal ions and a metal substrate: Differently substituted cobalt porphyrins on Ag(111)

    Energy Technology Data Exchange (ETDEWEB)

    Bai, Yun; Buchner, Florian; Schmid, Martin; Kellner, Ina; Vollnhals, Florian; Marbach, Hubertus; Steinrueck, Hans-Peter; Gottfried, J. Michael [Universitaet Erlangen-Nuernberg, Lehrstuhl fuer Physikalische Chemie II, Egerlandstr. 3, 91058 Erlangen (Germany)

    2009-07-01

    Adsorbed metalloporphyrins are of increasing interest due to their potential applications in heterogeneous catalysis and in sensor systems. Previous studies from our group have suggested the existence of an electronic interaction between the metal centers of the adsorbed porphyrin complexes of iron and cobalt and the underlying substrate surface, which plays an important role in modifying the electronic structure and, thereby, the reactivity of these metal centers. However, with the previously used tetraphenylporphyrin (TPP) ligands, the adsorbed complexes undergo saddle-shape distortion, which could also influence the electronic structure. To separate the effects of distortion on the one hand and the coupling to the substrate on the other, we have studied cobalt octaethylporphyrin, which adsorbs in a flat, undistorted conformation on Ag(111). Comparison of our XPS, UPS, and STM results with previous CoTPP data confirms that indeed the metal center plays an essential role in the electronic interaction between the porphyrin complexes and the substrate.

  20. Hydrated and Solvated Tin(II) Ions in Solution and the Solid State, and a Coordination Chemistry Overview of the d10s2Metal Ions.

    Science.gov (United States)

    Persson, Ingmar; D'Angelo, Paola; Lundberg, Daniel

    2016-12-19

    The coordination chemistry of d 10 s 2 metal ions is strongly affected by an (at least partially) occupied d 10 s 2 metal ion-ligand atom antibonding orbital, which may cause a void in the coordination sphere due to repulsion between the electrons in the antibonding orbital on the metal ion and those on the ligands. The character of the formed d 10 s 2 metal ion-ligand atom bond plays an important role in the electron density in the antibonding orbital and thereby also in the coordination chemistry. The hydrated tin(II) ion, [Sn(H 2 O) 3 ] 2+ , and the trihydroxidostannate ion, [Sn(OH) 3 ] - , have very different mean Sn-O bond lengths (2.21 and 2.08 Å, respectively) and O-Sn-O angles (ca. 78 and 90°, respectively) both in the solid state and in solution. On increasing the covalency of the tin(II)-ligand bonds, the repulsion decreases and higher coordination numbers are obtained, as seen in the dimethylsulfoxide- and N,N-dimethylthioformamide-solvated tin(II) ions, both of which are five-coordinate with square-pyramidal structures. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Carbohydrate-linked asparagine-101 of prothrombin contains a metal ion protected acetylation site. Acetylation of this site causes loss of metal ion induced protein fluorescence change

    Energy Technology Data Exchange (ETDEWEB)

    Welsch, D.J.; Nelsestuen, G.L.

    1988-06-28

    Prothrombin fragment 1 (prothrombin residues 1-156) contains two acetylation sites that are protected from derivatization by calcium. The first site was protected by only calcium while the second site was protected by magnesium as well. To identify this second acetylation site, fragment 1 was first acetylated with unlabeled reagent in the presence of magnesium. Metal ions were removed, and the protein was acetylated with radiolabeled reagent. The incorporated radiolabel was stable over long periods of time and at acidic or basic pH as long as elevated temperatures were avoided. The radiolabel was removed by treatment of the protein at pH 10 and 50 /sup 0/C or with 0.2 M hydroxylamine at 50 /sup 0/C for at least 30 min. Proteolytic degradation of the protein showed that the radioactivity appeared in a tryptic peptide corresponding to residues 94-111 of prothrombin. Amino acid sequence analysis revealed that the radiolabel was associated with an unextracted sequence product. The major radiolabeled product contained Asn/sup 101/-Ser/sup 102/ along with the expected chitobiose attached to Asn-101. NMR analysis revealed the presence of three acetate groups which would correspond to two from the chitobiose plus the incorporated acetate residue. Mass spectral analysis showed the correct mass for this glycopeptide plus a single added acetyl group. Amide /sup 1/H NMR analysis showed only three amide protons rather than the anticipated four. On the basis of these several observations, it is postulated that the site of acetylation is the ..beta..-amide nitrogen of Asn-101. Consequently, these studies showed an unusual chemical reactivity in prothrombin fragment 1. They further show that metal ion binding to prothrombin fragment 1 and subsequent protein fluorescence quenching involve sites ion the kringle region of the protein.

  2. 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

    2017-11-27

    The first instance of an acidic aqueous biphasic system (AcABS) based on tributyltetradecyl phosphonium chloride ([P44414 ][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 CoII from NiII , here studied at 24 and 50 °C. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Cellulose Nanocrystals Obtained from Rice By-Products and Their Binding Potential to Metallic Ions

    Directory of Open Access Journals (Sweden)

    Vanessa L. Albernaz

    2015-01-01

    Full Text Available The present study aimed to develop and optimize a method to obtain cellulose nanocrystals from the agricultural by-products rice husk and straw and to evaluate their electrostructural modifications in the presence of metallic ions. First, different particle formation conditions and routes were tested and analyzed by spectrophotometry, dynamic light scattering (DLS, and Zeta potential measurements. Then, electrostructural effects of ions Na(I, Cd(II, and Al(III on the optimized nanoparticles were analyzed by atomic force microscopy (AFM, scanning electron microscopy (SEM, and electrical conductivity (EC assessments. The produced cellulose nanocrystals adopted a rod-like shape. AFM height distribution and EC data indicated that the nanocrystals have more affinity in binding with Na(I > Al(III > Cd(II. These data suggest that the use of these cellulose nanocrystals in the bioremediation field is promising, both in metal sorption from wastewater and as an alternative for water desalination.

  4. Computer optimization of background electrolyte composition in the separation of metal ions by capillary electrophoresis.

    Science.gov (United States)

    Billiet, H A; Andersson, P E; Haddad, P R

    1996-08-01

    The iterative regression design developed earlier for high performance liquid chromatography (HPLC) has been applied successfully to the optimization of the separation of 11 metal ions by capillary electrophoresis. The parameters used for optimization were pH (over the range 3.5-5.0) and the concentration of 2-hydroxyisobutyric acid (HIBA) (2-20 mM) used as the complex-forming ligand added to the background electrolyte. Five initial experiments were performed and the response surface was calculated using the relative resolution product as criterion. Three additional experiments were sufficient to establish a stable optimum, with which all 11 metal ions were separated and well spread in the electropherogram. The total analysis time was less than 5 min.

  5. Multicharged ion-induced emission from metal- and insulator surfaces related to magnetic fusion research

    Energy Technology Data Exchange (ETDEWEB)

    Winter, H.P. [Technische Univ., Vienna (Austria). Inst. fuer Allgemeine Physik

    1997-01-01

    The edge region of magnetically confined plasmas in thermonuclear fusion experiments couples the hot plasma core with the cold first wall. We consider the dependence of plasma-wall interaction processes on edge plasma properties, with particular emphasis on the role of slow multicharged ions (MCI). After a short survey on the physics of slow MCI-surface interaction we discuss recent extensive studies on MCI-induced electron emission from clean metal surfaces conducted at impact velocities << 1 a.u., from which generally reliable total electron yields can be obtained. We then demonstrate the essentially different role of the MCI charge for electron emission from metallic and insulator surfaces, respectively. Furthermore, we present recent results on slow MCI-induced `potential sputtering` of insulators which, in contrast to the well established kinetic sputtering, already occurs at very low ion impact energy and strongly increases with the MCI charge state. (J.P.N.). 55 refs.

  6. NANOSTRUCTURED METAL OXIDES FOR ANODES OF LI-ION RECHARGEABLE BATTERIES

    Energy Technology Data Exchange (ETDEWEB)

    Au, M.

    2009-12-04

    The aligned nanorods of Co{sub 3}O{sub 4} and nanoporous hollow spheres (NHS) of SnO{sub 2} and Mn{sub 2}O{sub 3} were investigated as the anodes for Li-ion rechargeable batteries. The Co{sub 3}O{sub 4} nanorods demonstrated 1433 mAh/g reversible capacity. The NHS of SnO{sub 2} and Mn{sub 2}O{sub 3} delivered 400 mAh/g and 250 mAh/g capacities respectively in multiple galvonastatic discharge-charge cycles. It was found that high capacity of NHS of metal oxides is sustainable attributed to their unique structure that maintains material integrity during cycling. The nanostructured metal oxides exhibit great potential as the new anode materials for Li-ion rechargeable batteries with high energy density, low cost and inherent safety.

  7. Metal-ion catalyzed polymerization in the eutectic phase in water-ice

    DEFF Research Database (Denmark)

    Monnard, Pierre-Alain; Szostak, Jack W.

    2008-01-01

    the main issue preventing an efficient template-directed RNA polymerization. We report here the investigation of template-directed RNA polymerization in the eutectic phase in water-ice. In particular, it was found that activated Uridilate monomers in the presence of metal-ion catalysts could efficiently...... elongate RNA hairpins whose 5’-overhangs served as the templating sequence. The same applies for every other pyrimidine and purine nucleobase. Moreover, the initial elongation rates were always higher in the presence of a template complementary to the nucleotide than in systems without proper base......-pairing opportunities. These results suggest that a template-directed RNA polymerization catalyzed by metal-ions could be carried out under eutectic phase in water-ice conditions....

  8. Effective optical Faraday rotations of semiconductor EuS nanocrystals with paramagnetic transition-metal ions.

    Science.gov (United States)

    Hasegawa, Yasuchika; Maeda, Masashi; Nakanishi, Takayuki; Doi, Yoshihiro; Hinatsu, Yukio; Fujita, Koji; Tanaka, Katsuhisa; Koizumi, Hitoshi; Fushimi, Koji

    2013-02-20

    Novel EuS nanocrystals containing paramagnetic Mn(II), Co(II), or Fe(II) ions have been reported as advanced semiconductor materials with effective optical rotation under a magnetic field, Faraday rotation. EuS nanocrystals with transition-metal ions, EuS:M nanocrystals, were prepared by the reduction of the Eu(III) dithiocarbamate complex tetraphenylphosphonium tetrakis(diethyldithiocarbamate)europium(III) with transition-metal complexes at 300 °C. The EuS:M nanocrystals thus prepared were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), inductively coupled plasma atomic emission spectroanalysis (ICP-AES), and a superconducting quantum interference device (SQUID) magnetometer. Enhanced Faraday rotations of the EuS:M nanocrystals were observed around 550 nm, and their enhanced spin polarization was estimated using electron paramagnetic resonance (EPR) measurements. In this report, the magneto-optical relationship between the Faraday rotation efficiency and spin polarization is discussed.

  9. New Insight into Metal Ion-Driven Catalysis of Nucleic Acids by Influenza PA-Nter.

    Directory of Open Access Journals (Sweden)

    Daria Kotlarek

    Full Text Available PA subunit of influenza RNA-dependent RNA polymerase deserves constantly increasing attention due to its essential role in influenza life cycle. N-terminal domain of PA (PA-Nter harbors endonuclease activity, which is indispensable in viral transcription and replication. Interestingly, existing literature reports on in vitro ion preferences of the enzyme are contradictory. Some show PA-Nter activity exclusively with Mn2+, whereas others report Mg2+ as a natural cofactor. To clarify it, we performed a series of experiments with varied ion concentrations and substrate type. We observed cleavage in the presence of both ions, with a slight preference for manganese, however PA-Nter activity highly depended on the amount of residual, co-purified ions. Furthermore, to quantify cleavage reaction rate, we applied fluorescence cross-correlation spectroscopy (FCCS, providing highly sensitive and real-time monitoring of single molecules. Using nanomolar ssDNA in the regime of enzyme excess, we estimated the maximum reaction rate at 0.81± 0.38 and 1.38± 0.34 nM/min for Mg2+ and Mn2+, respectively. However, our calculations of PA-Nter ion occupancy, based on thermodynamic data, suggest Mg2+ to be a canonical metal in PA-Nter processing of RNA in vivo. Presented studies constitute a step toward better understanding of PA-Nter ion-dependent activity, which will possibly contribute to new successful inhibitor design in the future.

  10. Effect on uptake of heavy metal ions by phosphate grafting of allophane.

    Science.gov (United States)

    Okada, Kiyoshi; Nishimuta, Koji; Kameshima, Yoshikazu; Nakajima, Akira

    2005-06-15

    The effect of phosphate grafting on the uptake of various heavy metal ions was investigated using allophane, a clay mineral having a chemical composition of 1-2SiO2Al2O3.5-6H2O with hollow nanoparticles 3.5-5 nm in size. Phosphate grafting was performed on allophane with an atomic ratio Si/Al=0.85 using the orthophosphates (NH4)2HPO4, Na2HPO4 and CaHPO4 and the triphosphate Na5P3O10. The cations in the phosphates were partially retained in the samples, along with the grafted phosphate. Uptake experiments were performed with various heavy metal ions (Cu2+, Zn2+, Ni2+, Co2+, and Mn2+) and alkaline earth ions (Mg2+ and Ca2+) using a batch method. With increasing amounts of grafted phosphate, the Cu2+ uptake capacity increases to about double of that of ungrafted allophane. Although part of the grafted phosphate is released during the uptake experiments, this can be largely suppressed by heat-treating the samples at 200-500 degrees C. The Cu2+ uptake ability of the (NH4)2HPO4-grafted sample showed a steep decrease with higher heating temperature according to the thermal decomposition of NH4+. The ratios of cations released from the samples to cations removed from solution (2Na/Cu and Ca/Cu) are close to unity. From these results, the replacement reaction is thought to be the main uptake mechanism of heavy metal ions in the present samples. The uptake abilities of the present samples for various cations are explained with respect to the solubilities of the corresponding metal phosphates.

  11. Synthesis of Zeolite from Fly Ash and Removal of Heavy Metal Ions from Newly Synthesized Zeolite

    OpenAIRE

    Solanki, Parag; Gupta, Vikal; Kulshrestha, Ruchi

    2010-01-01

    Coal fly ash was used to synthesize X-type zeolite by alkali fusion followed by hydrothermal treatment. Characteristics of the various Fly ash samples were carried out. Coal proximate analysis was done. Batch experiment was carried out for the adsorption of some heavy metal ions on to synthesized Zeolite. The cost of synthesized zeolite was estimated to be almost one-fifth of that of commercial 13X zeolite available in the market.

  12. Clean and efficient extraction of copper ions and deposition as metal

    OpenAIRE

    Hassan H. Elsentriecy; Abraham F. Jalbout; Dominic F. Gervasio

    2015-01-01

    A simple, clean and efficient one-pot process is offered as an alternative to the conventional complex processing presently used to extract copper ions from copper containing materials, like copper concentrate or slag, and to form copper metal. The alternative process uses a eutectic molten salt of potassium chloride, sodium chloride and zinc chloride as the reaction fluid which is recyclable, low in cost, environmentally benign, low melting (melting point 204°), high boiling (vapor pressure ...

  13. 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.

  14. Synthesis of Zeolite from Fly Ash and Removal of Heavy Metal Ions from Newly Synthesized Zeolite

    Directory of Open Access Journals (Sweden)

    Parag Solanki

    2010-01-01

    Full Text Available Coal fly ash was used to synthesize X-type zeolite by alkali fusion followed by hydrothermal treatment. Characteristics of the various Fly ash samples were carried out. Coal proximate analysis was done. Batch experiment was carried out for the adsorption of some heavy metal ions on to synthesized Zeolite. The cost of synthesized zeolite was estimated to be almost one-fifth of that of commercial 13X zeolite available in the market.

  15. Investigation of complexing ability of ionites with various groups to some heavy and transition metal ions

    Directory of Open Access Journals (Sweden)

    Yedil Yergozhin

    2013-05-01

    Full Text Available The physico-chemical and complexing properties of the sorbent based on chloromethylated styrene and divinylbenzene copolymer with nicotinamide groups and copolymers based on metacryloilaminobenzene acids with 2-methyl-5-vinylpyridineisomers are studied. By potentiometric titration method the constant of polyelectrolytes functional groups ionization, the composition and strength of the resulting complexes with ions of some heavy and transition metals are determined.

  16. Effects of metal nanoparticles on the secondary ion yields of a model alkane molecule upon atomic and polyatomic projectiles in secondary ion mass spectrometry.

    Science.gov (United States)

    Wehbe, Nimer; Heile, Andreas; Arlinghaus, Heinrich F; Bertrand, Patrick; Delcorte, Arnaud

    2008-08-15

    A model alkane molecule, triacontane, is used to assess the effects of condensed gold and silver nanoparticles on the molecular ion yields upon atomic (Ga(+) and In(+)) and polyatomic (C60(+) and Bi3(+)) ion bombardment in metal-assisted secondary ion mass spectrometry (MetA-SIMS). Molecular films spin-coated on silicon were metallized using a sputter-coater system, in order to deposit controlled quantities of gold and silver on the surface (from 0 to 15 nm equivalent thickness). The effects of gold and silver islets condensed on triacontane are also compared to the situation of thin triacontane overlayers on metallic substrates (gold and silver). The results focus primarily on the measured yields of quasi-molecular ions, such as (M - H)(+) and (2M - 2H)(+), and metal-cationized molecules, such as (M + Au)(+) and (M + Ag)(+), as a function of the quantity of metal on the surface. They confirm the absence of a simple rule to explain the secondary ion yield improvement in MetA-SIMS. The behavior is strongly dependent on the specific projectile/metal couple used for the experiment. Under atomic bombardment (Ga(+), In(+)), the characteristic ion yields an increase with the gold dose up to approximately 6 nm equivalent thickness. The yield enhancement factor between gold-metallized and pristine samples can be as large as approximately 70 (for (M - H)(+) under Ga(+) bombardment; 10 nm of Au). In contrast, with cluster projectiles such as Bi3(+) and C60(+), the presence of gold and silver leads to a dramatic molecular ion yield decrease. Cluster projectiles prove to be beneficial for triacontane overlayers spin-coated on silicon or metal substrates (Au, Ag) but not in the situation of MetA-SIMS. The fundamental difference of behavior between atomic and cluster primary ions is tentatively explained by arguments involving the different energy deposition mechanisms of these projectiles. Our results also show that Au and Ag nanoparticles do not induce the same behavior in Met

  17. Interaction of 3d transition metal atoms with charged ion projectiles from Electron Nuclear Dynamics computation

    Science.gov (United States)

    Hagelberg, Frank

    2003-03-01

    Computational results on atomic scattering between charged projectiles and transition metal target atoms are presented. This work aims at obtaining detailed information about charge, spin and energy transfer processes that occur between the interacting particles. An in-depth understanding of these phenomena is expected to provide a theoretical basis for the interpretation of various types of ion beam experiments, ranging from gas phase chromatography to spectroscopic observations of fast ions in ferromagnetic media. This contribution focuses on the scattering of light projectiles ranging from He to O, that are prepared in various initial charge states, by 3d transition metal atoms. The presented computations are performed in the framework of Electron Nuclear Dynamics (END)^1 theory which incorporates the coupling between electronic and nuclear degrees of freedom without reliance on the computationally cumbersome and frequently intractable determination of potential energy surfaces. In the present application of END theory to ion - transition metal atom scattering, a supermolecule approach is utilized in conjunction with a spin-unrestricted single determinantal wave function describing the electronic system. Integral scattering, charge and spin exchange cross sections are discussed as functions of the elementary parameters of the problem, such as projectile and target atomic numbers as well as projectile charge and initial kinetic energy. ^1 E.Deumens, A.Diz, R.Longo, Y.Oehrn, Rev.Mod.Phys. 66, 917 (1994)

  18. The role of metallic ions in nano-bio hybrid catalysts from ab initio first principles

    Science.gov (United States)

    Behera, Sushant; Deb, Pritam

    We employ high-accuracy linear-scaling density functional theory calculations with a near-complete basis set and a minimal parameter implicit solvent model, within the self-consistent calculation, on silver ion assimilated on bacteriorhodopsin (bR) at specific binding sites. The geometry optimization indicates the formation of stable active sites at the interface of nano-bio hybrid and density of states reflects the metallic behavior of the active sites. Detailed kinetics of the catalytic reaction is revealed using ab initio electronic structure calculations. We observed that the metal ion incorporated active sites are more efficient in electrolytic splitting of water than pristine sites due to their less value of Gibbs free energy for hydrogen evolution reaction and strong synergistic effect. The volcano plot analysis and free energy diagram are considered to understan hydrogen evolution efficiency. Moreover, the essential role of metallic ion on catalytic efficiency is elucidated. DBT, Government of India, vide Grant No BT/357/NE/TBP/ 2012. DST, GoI for financial support under INSPIRE Fellowship(IF150325).

  19. 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.

  20. Postage stamp-sized array sensor for the sensitive screening test of heavy-metal ions.

    Science.gov (United States)

    Zhang, Yu; Li, Xiao; Li, Hui; Song, Ming; Feng, Liang; Guan, Yafeng

    2014-10-07

    The sensitive determination of heavy-metal ions has been widely investigated in recent years due to their threat to the environment and to human health. Among various analytical detection techniques, inexpensive colorimetric testing papers/strips play a very important role. The limitation, however, is also clear: the sensitivity is usually low and the selectivity is poor. In this work, we have developed a postage stamp-sized array sensor composed of nine commercially available heterocyclic azo indicators. Combining filtration-based enrichment with an array of technologies-based pattern-recognition, we have obtained the discrimination capability for seven heavy-metal ions (Hg(2+), Pb(2+), Ag(+), Ni(2+), Cu(2+), Zn(2+), and Co(2+)) at their Chinese wastewater discharge standard concentrations. The allowable detection level of Hg(2+) was down to 0.05 mg L(-1). The heavy-metal ions screening test was readily achieved using a standard chemometric approach. And the array sensor applied well in real water samples.

  1. Adsorption of heavy metal ions by hierarchically structured magnetite-carbonaceous spheres.

    Science.gov (United States)

    Gong, Jingming; Wang, Xiaoqing; Shao, Xiulan; Yuan, Shuang; Yang, Chenlin; Hu, Xianluo

    2012-11-15

    Magnetically driven separation technology has received considerable attention in recent decade for its great potential application. In this work, hierarchically structured magnetite-carbonaceous microspheres (Fe(3)O(4)-C MSs) have been synthesized for the adsorption of heavy metal ions from aqueous solution. Each sphere contains numerous unique rattle-type structured magnetic particles, realizing the integration of rattle-type building unit into microspheres. The as-prepared composites with high BET surface area, hierarchical as well as mesoporous structures, exhibit an excellent adsorption capacity for heavy metal ions and a convenient separation procedure with the help of an external magnet. It was found that the maximum adsorption capacity of the composite toward Pb(2+) was ∼126mgg(-1), displaying a high efficiency for the removal of heavy metal ions. The Freundlich adsorption isotherm was applicable to describe the removal processes. Kinetics of the Pb(2+) removal was found to follow pseudo-second-order rate equation. The as-prepared composite of Fe(3)O(4)-C MSs as well as Pb(2+)-adsorbed composite were carefully examined by scanning electron microscopy (SEM), Zeta potential measurements, Fourier transform infrared spectroscopy (FT-IR), nitrogen sorption measurements, and X-ray photoelectron spectroscopy (XPS). Based on the characterization results, a possible mechanism of Pb(2+) removal with the composite of Fe(3)O(4)-C MSs was proposed. Copyright © 2012 Elsevier B.V. All rights reserved.

  2. Polydopamine-mediated surface-functionalization of graphene oxide for heavy metal ions removal

    Science.gov (United States)

    Dong, Zhihui; Zhang, Feng; Wang, Dong; Liu, Xia; Jin, Jian

    2015-04-01

    By utilizing polydopamine (PD) nano-thick interlayer as mediator, polyethylenimine (PEI) brushes with abundant amine groups were grafted onto the surface of PD coated graphene oxide (GO) uniformly via a Michael-Addition reaction and produced a PEI-PD/GO composite nanosheets. The PEI-PD/GO composite exhibited an improved performance for adsorption of heavy metal ions as compared to PEI-coated GO and pure GO. The adsorption capacities for Cu2+, Cd2+, Pb2+, Hg2+ are up to 87, 106, 197, and 110 mg/g, respectively. To further make the GO based composite operable, PEI-PD/RGO aerogel was prepared through hydrothermal and achieved a high surface area up to 373 m2/g. Although the adsorption capacity of PEI-PD/RGO aerogel for heavy metal ions decreases a little as compared to PEI-PD/GO composite dispersion (38, 32, 95, 113 mg/g corresponding to Cu2+, Cd2+, Pb2+, and Hg2+, respectively), it could be recycled several times in a simple way by releasing adsorbed metal ions, indicating its potential application for cleaning wastewater.

  3. Effect of pH and metal ions on the decomposition rate of S-nitrosocysteine.

    Science.gov (United States)

    Gu, Jun; Lewis, Randy S

    2007-09-01

    S-nitrosothiols (RSNOs) have many biological functions including platelet deactivation, immunosupression, neurotransmission, and host defense. Most of the functions are attributed to nitric oxide (NO) release during S-nitrosothiol decomposition. As the simplest biologically occurring S-nitrosothiol, S-nitrosocysteine (CySNO) has been widely used as an NO donor and has also been incorporated into biomedical polymers. Knowledge of the CySNO decomposition rate is important for assessing the impact of CySNO on various bioengineering applications or biological systems. In this work, spectrophotometer measurements of CySNO decomposition in the presence of metal ions showed that the decomposition rate is highly susceptible to the pH. The maximum decomposition occurs near physiological pH (near 7.4) while in the acidic (pH pH > 9) condition CySNO is very stable. This demonstrates that blood provides an optimized environment for the decomposition of CySNO leading to the release of NO. The CySNO decomposition rate can also be affected by buffers with different purity levels in the presence and absence of metal ion chelators-although all buffers show the same pH phenomenon of maximizing near physiological pH. An equilibrium model of metal ions as a function of pH provides a plausible explanation for the pH dependence on the experimental decomposition rate.

  4. Efficient removal of heavy metal ions from aqueous solution using salicylic acid type chelate adsorbent.

    Science.gov (United States)

    An, Fuqiang; Gao, Baojiao; Dai, Xin; Wang, Min; Wang, Xiaohua

    2011-09-15

    In this study, 5-aminosalicylic acid was successfully grafted onto the poly(glycidyl methacrylate) (PGMA) macromolecular chains of PGMA/SiO(2) to obtain a novel adsorbent designated as ASA-PGMA/SiO(2). The adsorption properties of ASA-PGMA/SiO(2) for heavy metal ions were studied through batch and column methods. The experimental results showed that ASA-PGMA/SiO(2) possesses strong chelating adsorption ability for heavy metal ions, and its adsorption capacity for Cu(2+), Cd(2+), Zn(2+), and Pb(2+) reaches 0.42, 0.40, 0.35, and 0.31 mmol g(-1), respectively. In addition, pH has a great influence on the adsorption capacity in the studied pH range. The adsorption isotherm data greatly obey the Langmuir and Freundlich model. The desorption of metal ions from ASA-PGMA/SiO(2) is effective using 0.1 mol l(-1) of hydrochloric acid solution as eluent. Consecutive adsorption-desorption experiments showed that ASA-PGMA/SiO(2) could be reused almost without any loss in the adsorption capacity. Copyright © 2011 Elsevier B.V. All rights reserved.

  5. Ion conductivity and transport by porous coordination polymers and metal-organic frameworks.

    Science.gov (United States)

    Horike, Satoshi; Umeyama, Daiki; Kitagawa, Susumu

    2013-11-19

    Ion conduction and transport in solids are both interesting and useful and are found in widely distinct materials, from those in battery-related technologies to those in biological systems. Scientists have approached the synthesis of ion-conductive compounds in a variety of ways, in the areas of organic and inorganic chemistry. Recently, based on their ion-conducting behavior, porous coordination polymers (PCPs) and metal-organic frameworks (MOFs) have been recognized for their easy design and the dynamic behavior of the ionic components in the structures. These PCP/MOFs consist of metal ions (or clusters) and organic ligands structured via coordination bonds. They could have highly concentrated mobile ions with dynamic behavior, and their characteristics have inspired the design of a new class of ion conductors and transporters. In this Account, we describe the state-of-the-art of studies of ion conductivity by PCP/MOFs and nonporous coordination polymers (CPs) and offer future perspectives. PCP/MOF structures tend to have high hydrophilicity and guest-accessible voids, and scientists have reported many water-mediated proton (H(+)) conductivities. Chemical modification of organic ligands can change the hydrated H(+) conductivity over a wide range. On the other hand, the designable structures also permit water-free (anhydrous) H(+) conductivity. The incorporation of protic guests such as imidazole and 1,2,4-triazole into the microchannels of PCP/MOFs promotes the dynamic motion of guest molecules, resulting in high H(+) conduction without water. Not only the host-guest systems, but the embedding of protic organic groups on CPs also results in inherent H(+) conductivity. We have observed high H(+) conductivities under anhydrous conditions and in the intermediate temperature region of organic and inorganic conductors. The keys to successful construction are highly mobile ionic species and appropriate intervals of ion-hopping sites in the structures. Lithium (Li

  6. Electrophoretic studies of polygalacturonate oligomers and their interactions with metal ions.

    Science.gov (United States)

    Wiedmer, S K; Cassely, A; Hong, M; Novotny, M V; Riekkola, M L

    2000-09-01

    Polygalacturonic acid, a linear homopolysaccharide, was investigated by capillary electrophoresis (CE) using linear polyacrylamide-coated capillaries and laser-induced fluorescence (LIF) detection. A successful separation of its fluorescently labeled oligomers was achieved through sieving in polyacrylamide entangled matrices. The reaction conditions for the derivatization of polygalacturonic acid were optimized. In studying the interactions between polygalacturonic acid and various metal ions, the end-label, free-solution electrophoretic (ELFSE) technique, developed earlier in our laboratory (Sudor, J., Novotny, M. V., Anal. Chem. 1995, 67, 4205-4209) was found preferable to the sieving method. ELFSE is fast and convenient in that no polymer solutions are needed for the separation. The investigation showed that for the moderately large oligomers, the strongest binding occurred with calcium and cadmium ions, while the smallest interaction was observed with magnesium ions.

  7. Influence of implantation of three metallic ions on the mechanical properties of two polymers

    Energy Technology Data Exchange (ETDEWEB)

    Swain, M.V. [Commonwealth Scientific and Industrial Research Organisation (CSIRO), Lindfield, NSW (Australia). Div. of Applied Physics; Perry, A.J. [Australian National Univ., Canberra, ACT (Australia); Treglio, J.R.

    1996-12-31

    Ion implantation of poly ethylene terephthalate (PET) and polystyrene (PS) with various high energy metallic ions at 70 kV to dose of 3 x 10{sup 16} ions/cm 2 have been made. Measurements of the mechanical properties of the polymers before and after implantation have been made with an ultra microindentation system using both pointed and a small (2 nm) radiused spherical tipped indenter. Significant differences have been observed between the Ti-B dual implanted surfaces and those of the Au and W implanted surfaces. For both the PET and PS the resistance to indenter penetration at very low loads was much greater for the Ti-B dual implanted surfaces. The estimated hardness and modulus versus depth of penetration for both indenters shows that the spherical indenter produces more consistent and less controversial values that are somewhat lower than the optimistic estimates from pointed indenters. 8 refs., 2 fig.

  8. A chiral lanthanide metal-organic framework for selective sensing of Fe(iii) ions.

    Science.gov (United States)

    Zhao, Xiao-Lin; Tian, Dan; Gao, Qiang; Sun, Hong-Wei; Xu, Jian; Bu, Xian-He

    2016-01-21

    A new luminescent lanthanide metal-organic framework was synthesized under hydrothermal conditions by introducing the tetracarboxylic acid ligand (H4bptc) as a chromophore to sensitize the luminescence of the Tb(3+) ion. Interestingly, despite the achiral nature of H4bptc, the resulting framework exhibited rare chiral helical channels. The luminescence studies revealed that this material showed a highly selective fluorescence quenching response to Fe(3+) ions in liquid suspension, which can be conveniently observed by the naked eye under UV light. Thus, this material can be potentially used as a chemosensor for sensing Fe(3+) ions and its selective luminescence quenching response can be explained in terms of the competitive absorption mechanism.

  9. Chelate-free metal ion binding and heat-induced radiolabeling of iron oxide nanoparticles.

    Science.gov (United States)

    Boros, Eszter; Bowen, Alice M; Josephson, Lee; Vasdev, Neil; Holland, Jason P

    2015-01-01

    A novel reaction for chelate-free, heat-induced metal ion binding and radiolabeling of ultra-small paramagnetic iron oxide nanoparticles (USPIOs) has been established. Radiochemical and non-radioactive labeling studies demonstrated that the reaction has a wide chemical scope and is applicable to p-, d- and f-block metal ions with varying ionic sizes and formal oxidation states from 2+ to 4+. Radiolabeling studies found that 89Zr-Feraheme (89Zr-FH or 89Zr-ferumoxytol) can be isolated in 93 ± 3% radiochemical yield (RCY) and >98% radiochemical purity using size-exclusion chromatography. 89Zr-FH was found to be thermodynamically and kinetically stable in vitro using a series of ligand challenge and plasma stability tests, and in vivo using PET/CT imaging and biodistribution studies in mice. Remarkably, ICP-MS and radiochemistry experiments showed that the same reaction conditions used to produce 89Zr-FH can be employed with different radionuclides to yield 64Cu-FH (66 ± 6% RCY) and 111In-FH (91 ± 2% RCY). Electron magnetic resonance studies support a mechanism of binding involving metal ion association with the surface of the magnetite crystal core. Collectively, these data suggest that chelate-free labeling methods can be employed to facilitate clinical translation of a new class of multimodality PET/MRI radiotracers derived from metal-based nanoparticles. Further, this discovery is likely to have broader implications in drug delivery, metal separation science, ecotoxicology of nanoparticles and beyond.

  10. Effect of denture cleansers on metal ion release and surface roughness of denture base materials.

    Science.gov (United States)

    Davi, Letícia Resende; Felipucci, Daniela Nair Borges; de Souza, Raphael Freitas; Bezzon, Osvaldo Luiz; Lovato-Silva, Cláudia Helena; Pagnano, Valéria Oliveira; Paranhos, Helena de Freitas Oliveira

    2012-01-01

    Chemical disinfectants are usually associated with mechanical methods to remove stains and reduce biofilm formation. This study evaluated the effect of disinfectants on release of metal ions and surface roughness of commercially pure titanium, metal alloys, and heat-polymerized acrylic resin, simulating 180 immersion trials. Disk-shaped specimens were fabricated with commercially pure titanium (Tritan), nickel-chromium-molybdenum-titanium (Vi-Star), nickel-chromium (Fit Cast-SB Plus), and nickel-chromium-beryllium (Fit Cast-V) alloys. Each cast disk was invested in the flasks, incorporating the metal disk to the heat-polymerized acrylic resin. The specimens (n=5) were immersed in these solutions: sodium hypochlorite 0.05%, Periogard, Cepacol, Corega Tabs, Medical Interporous, and Polident. Deionized water was used as a control. The quantitative analysis of metal ion release was performed using inductively coupled plasma mass spectrometry (ELAN DRC II). A surface analyzer (Surftest SJ-201P) was used to measure the surface roughness (µm). Data were recorded before and after the immersions and evaluated by two-way ANOVA and Tukey's test (α=0.05). The nickel release proved most significant with the Vi-Star and Fit Cast-V alloys after immersion in Medical Interporous. There was a significant difference in surface roughness of the resin (p=0.011) after immersion. Cepacol caused significantly higher resin roughness. The immersion products had no influence on metal roughness (p=0.388). It could be concluded that the tested alloys can be considered safe for removable denture fabrication, but disinfectant solutions as Cepacol and Medical Interporous tablet for daily denture immersion should be used with caution because it caused greater resin surface roughness and greater ion release, respectively.

  11. Roles of metal ion complexation and membrane permeability in the metal flux through lipophilic membranes. Labile complexes at permeation liquid membranes

    NARCIS (Netherlands)

    Zhang, Z.; Buffle, J.; Leeuwen, van H.P.; Wojciechowski, K.

    2006-01-01

    The various physicochemical factors that influence the flux of carrier-transported metal ions through permeation liquid membranes (PLM) are studied systematically. Understanding PLM behavior is important (i) to optimize the application of PLM as metal speciation sensors in environmental media and

  12. P and Si functionalized MXenes for metal-ion battery applications

    KAUST Repository

    Zhu, Jiajie

    2017-04-10

    MXenes are a family of two-dimensional materials, composed of early transition metal carbides, nitrides, and carbonitrides, with great potential in energy storage systems, in particular in electrodes for Li, Na, K-ion batteries. However, so far the capacities are not competitive. In this context, we investigate P and Si functionalized MXenes for metal-ion battery applications, using first-principles calculations, since P and Si provide reaction products with high ion content. Replacement of the F and OH ligands of Ti2C and V2C with P and Si is demonstrated to be feasible (energy barriers of less than 0.128 eV) and the ion diffusion barriers turn out to be less than 0.32 eV. Importantly, the Li, Na, and K capacities are predicted to be 1767 mAh g−1, 711 mAh g−1, and 711 mAh g−1, respectively, thus being much higher than in the case of F and OH functionalization.

  13. Supplementation of soft drinks with metallic ions reduces dissolution of bovine enamel

    Directory of Open Access Journals (Sweden)

    Heloisa Aparecida Barbosa da Silva Pereira

    2013-07-01

    Full Text Available OBJECTIVE: The aim of this study was to evaluate the effect of the addition of metallic ions to carbonated drinks on their erosive potential. MATERIAL AND METHODS: Powdered enamel was added to carbonated beverages (Coca-ColaTM or Sprite ZeroTM and shaken for 30 s. The samples were then immediately centrifuged and the supernatant removed. This procedure was repeated 5 times with the beverages containing Cu2+, Mg2+, Mn2+ or Zn2+ (1.25-60 mmol/L. For Coca-ColaTM, the concentration of each ion that exhibited the highest protection was also evaluated in combination with Fe2+. The phosphate or calcium released were analyzed spectrophotometrically. Data were analyzed using ANOVA and Tukey's test (p<0.05. RESULTS: For Coca-ColaTM, the best protective effect was observed for Zn2+ alone (10 mmol/L or in combination (1 mmol/L with other ions (12% and 27%, respectively, when compared with the control. Regarding Sprite ZeroTM, the best protective effect was observed for Cu2+ at 15 and 30 mmol/L, which decreased the dissolution by 22-23%. Zn2+ at 2.5 mmol/L also reduced the dissolution of powdered enamel by 8%. CONCLUSIONS: The results suggest that the combination of metallic ions can be an alternative to reduce the erosive potential of Coca-ColaTM. Regarding Sprite ZeroTM, the addition of Cu2+ seems to be the best alternative.

  14. In situ cleaning of metal cathodes using a hydrogen ion beam

    Directory of Open Access Journals (Sweden)

    D. H. Dowell

    2006-06-01

    Full Text Available Metal photocathodes are commonly used in high-field rf guns because they are robust, straightforward to implement, and tolerate relatively poor vacuum compared to semiconductor cathodes. However, these cathodes have low quantum efficiency (QE even at UV wavelengths, and still require some form of cleaning after installation in the gun. A commonly used process for improving the QE is laser cleaning. In this technique the UV-drive laser is focused to a small diameter close to the metal’s damage threshold and then moved across the surface to remove contaminants. This method does improve the QE, but can produce nonuniform emission and potentially damage the cathode. Ideally, an alternative process which produces an atomically clean, but unaltered, surface is needed. In this paper we explore using a hydrogen ion (H-ion beam to clean a copper cathode. We describe QE measurements over the wavelength range of interest as a function of integrated exposure to an H-ion beam. We also describe the data analysis to obtain the work function and derive a formula of the QE for metal cathodes. Our measured work function for the cleaned sample is in good agreement with published values, and the theoretical QE as a function of photon wavelength is in excellent agreement with the cleaned copper experimental results. Finally, we propose an in situ installation of an H-ion gun compatible with existing s-band rf guns.

  15. Peculiarities and application perspectives of metal-ion implants in glasses

    Energy Technology Data Exchange (ETDEWEB)

    Mazzoldi, P.; Gonella, F. [Padua Univ. (Italy). Dipt. di Fisica; Arnold, G.W. [Sandia National Labs., Albuquerque, NM (United States); Battaglin, G. [Venice Univ. (Italy). Dipt. di Chimica Fisica; Bertoncello, R. [Padua Univ. (Italy). Dipt. di Chimica Inorganica, Metallorganica e Analitica

    1993-12-31

    Ion implantation in insulators causes modifications in the refractive-index as a result of radiation damage, phase separation, or compound formation. As a consequence, light waveguides may be formed with interesting applications in the field of optoelectronics. Recently implantation of metals ions (e.g. silver, copper, gold, lead,...) showed the possibility of small radii colloidal particles formation, in a thin surface layer of the glass substrate. These particles exhibit an electron plasmon resonance which depends on the optical constants of the implanted metal and on the refractive-index of the glass host. The non-linear optical properties of such colloids, in particular the enhancement of optical Kerr susceptibility, suggest that the, ion implantation technique may play an important role for the production of all-optical switching devices. In this paper an analysis of the state-of-the-art of the research in this field will be presented in the framework of ion implantation in glass physics and chemistry.

  16. Alginate-based nanocomposites for efficient removal of heavy metal ions.

    Science.gov (United States)

    Esmat, Mohamed; Farghali, Ahmed A; Khedr, Mohamed H; El-Sherbiny, Ibrahim M

    2017-09-01

    Cobalt ferrite nanoparticles (CF), titanate nanotubes (T), alginate (G) and their nanocomposite microparticles (CF/G and T/G) were prepared and used for efficient removal of Cu(2+), Fe(3+) and As(3+) ions from water. The nanocomposites were characterized using field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), FTIR and vibrating sample magnetometer (VSM). In addition, the effects of pH, contact time, adsorbent weight and heavy metal ion concentration on the removal efficiency were investigated. Our results revealed a successful preparation of the nanocomposite particles. The optimized batch experiment conditions were found to be pH of 6.5, contact time of 2h and adsorbent weight of 0.15g. The removal efficiencies for Cu(2+) using G, CF, T, CF/G and T/G were found to be 91%, 100%, 99.9%, 95% and 98%, respectively. While that of Fe(3+) removal was 60%, 100%, 100%, 60% and 82%, respectively. Efficient removal of As(3+) ions was also attained (98% upon using T nanoadsorbents). The current study demonstrated that the developed nanomaterials (CF and T) and their corresponding alginate-based nanocomposite microparticles could be further tailored and used as efficient adsorbents for the uptake of different heavy metal ions from wastewater. Copyright © 2017 Elsevier B.V. All rights reserved.

  17. Ion-induced effects on metallic nanoparticles; Ioneninduzierte Effekte an metallischen Nanoteilchen

    Energy Technology Data Exchange (ETDEWEB)

    Klimmer, Andreas

    2010-02-25

    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{sub 0} phase. (orig.)

  18. Profiling measurements of metal ion distribution in thin polymer inclusion membranes by Rutherford backscattering spectrometry

    Science.gov (United States)

    Guedioura, B.; Bendjaballah, N.; Alioui, N.

    2014-05-01

    Polymer inclusion membranes (PIMs) composed of a homogeneous mixture of cellulose triacetate matrix, 2-nitro-phenyl-octyl-ether as plasticizer and tri-octyl-phosphine-oxyde as carrier were synthesized by the spin coating method. Synthesized membranes were doped with molybdenum metal ions and then characterized by four experimental techniques: thermo gravimetric and differential analyses, scanning electron microscopy (SEM), attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy and Rutherford backscattering (RBS) spectrometry using a 3.2 MeV He+ ion beam. The RBS analysis has established both the elemental composition as well as the Mo+ metal profiling of the studied PIMs. The experimental irradiation conditions were optimized in order to determine the ion fluence thresholds resulting in measurable changes in elemental composition of membranes. Changes in physico-chemical properties of the irradiated PIMs vs He+ ion fluence were observed with the ATR-FTIR analysis. Also, the SEM analysis of PIMs surfaces has revealed a porous texture, while the thermal analysis of annealed PIMs at 105°C has showed no significant changes of mass (∼1%) of the studied samples.

  19. Redox Active Transition Metal ions Make Melanin Susceptible to Chemical Degradation Induced by Organic Peroxide.

    Science.gov (United States)

    Zadlo, Andrzej; Pilat, Anna; Sarna, Michal; Pawlak, Anna; Sarna, Tadeusz

    2017-12-01

    With aging, retinal pigment epithelium melanosomes, by fusion with the age pigment lipofuscin, form complex granules called melanolipofuscin. Lipofuscin granules may contain oxidized proteins and lipid hydroperoxides, which in melanolipofuscin could chemically modify melanin polymer, while transition metal ions present in melanin can accelerate such oxidative modifications. The aim of this research was to examine the effect of selected transition metal ions on melanin susceptibility to chemical modification induced by the water-soluble tert-butyl hydroperoxide used as an oxidizing agent. Synthetic melanin obtained by DOPA autooxidation and melanosomes isolated from bovine retinal pigment epithelium were analyzed. To monitor tert-butyl hydroperoxide-induced oxidative changes of DMa and BMs, electron paramagnetic resonance spectroscopy, UV-vis absorption spectroscopy, dynamic light scattering, atomic force microscopy and electron paramagnetic resonance oximetry were employed. These measurements revealed that both copper and iron ions accelerated chemical degradation induced by tert-butyl hydroperoxide, while zinc ions had no effect. Strong prooxidant action was detected only in the case of melanosomes and melanin degraded in the presence of iron. It can be postulated that similar chemical processes, if they occur in situ in melanolipofuscin granules of the human retinal pigment epithelium, would modify antioxidant properties of melanin and its reactivity.

  20. Effect of Metal Ions of Chlorapatites on the Topotaxial Replacement by Hydroxyapatite under Hydrothermal Conditions

    Science.gov (United States)

    Rendón-Angeles, J. C.; Yanagisawa, K.; Ishizawa, N.; Oishi, S.

    2000-11-01

    The effect of the metal ions in the chlorapatite structure on the topotaxial conversion to the hydroxyapatite structure was investigated, using three different types of chlorapatite single crystals, calcium, strontium, and barium chlorapatite. The topotaxial conversion to the hydroxyapatite structure was conducted under hydrothermal conditions at a range of temperature from 300 to 800°C for intervals between 3 and 96 h in concentrated KOH solutions. The Cl- ion exchange in the calcium and strontium chlorapatite crystals was completed at 500 and 700°C in a 6.25 M KOH solution, respectively, which resulted in the formation of hydroxyapatite structure. The transformed crystals retained their original shape and dimensions due to the topotaxial transformation. In contrast, the rate of the topotaxial conversion was further reduced on the barium chlorapatite crystals that contain metal ions with large size such as Ba. These crystals were only partially converted to hydroxyapatite even at 800°C in 10 M KOH solution. Under these conditions, a dissolution of ion species of the topotaxially converted barium hydroxyapatite layer was observed, which resulted in the precipitation of new crystals on the surface of the remaining barium chlorapatite crystals. The structure of the new crystals was matched with the hexagonal apatite structure, but a great amount of K was incorporated in the structure.